JP5537790B2 - Propylene surface protective film - Google Patents

Description

  The present invention relates to a film for protecting a propylene-based surface, and more specifically, for protecting a surface of a building member such as a synthetic resin plate, a decorative plate, a metal plate, and a glass plate, and a liquid crystal display component such as a polarizing plate and a retardation plate. The present invention relates to a propylene-based surface protective film that is suitably used for surface protection.

  Surface protection films are affixed to building materials such as synthetic resin plates and liquid crystal display parts of optical equipment members from the viewpoint of preventing scratches and dirt on the surface during processing, transportation and transportation, and after processing or transportation and transportation. It is common to peel off and use the surface protection film which concerns later.

  Conventionally, as the surface protective film, there is a surface protective film mainly composed of an ethylene-based resin. For example, a surface protective film made of an ethylene-based resin that is polymerized from a metallocene catalyst, has a narrow composition distribution and molecular weight distribution, and does not have fish eye is described (for example, see Patent Document 1). Further, a polyethylene composed of 50 to 90% by weight of a specific low density polyethylene and 10 to 50% by weight of a specific high density polyethylene having a weight average molecular weight / number average molecular weight ratio of 9 to 15, and an ethylene-unsaturated ester A laminated film obtained by coextruding an adhesive layer made of a copolymer is described (for example, see Patent Document 2).

However, in the surface protective film described in the above patent document, since polyethylene is the main component, retention occurs inside the molding machine extruder during film formation, gelation occurs due to deterioration of the ethylene component, Since the fish eye is generated, when the product is attached to the object to be protected and stacked and stored as it is, the object to be protected is dented due to the presence of the fish eye. Therefore, for example, even if an attempt is made to use the laminated film as a polarizing plate or a retardation plate used as a liquid crystal display material, there is a problem that the image is distorted due to the dents and cannot be applied.
In addition, in view of problems of heat resistance, scratch resistance, and rigidity of polyethylene, and having improved the point defects of the metal thin film layer due to the influence of chlorine ions, it is made of polypropylene having a chlorine content of 5 ppm by weight or less. A surface protective film containing a characteristic propylene-based resin as a main component has also been proposed (see, for example, Patent Document 3). However, even in the propylene-based resin described in the patent document, gelation like polyethylene does not occur, but the molecular weight distribution is wide, that is, low molecular weight having a low molecular weight and high molecular weight having a high molecular weight are mixed. Therefore, when the high molecular weight component is formed into a film, an unmelted fine lump becomes a fish eye and exists in the film, resulting in a dent in the protected object.

Further, both ethylene-based resins and propylene-based resins have a crystallinity distribution, but there is a problem that if the crystallinity distribution is wide and there are many low crystal components, the object to be protected is contaminated. In addition, in the process of producing the polymer, sticking of the low crystal component causes polymer adhesion in a polymerization tank or the like, resulting in deterioration of the polymer due to stagnation, and as a result, fish eyes derived from polymer degradation products exist in the film. As a result, the object to be protected is dented, and there is a problem that it cannot be applied as a surface protective film. In addition, if the crystallinity distribution is wide, the compatibility between the low crystallinity component and the high crystallinity component becomes non-uniform, and the high crystallinity component tends to exist as fish eyes in the form of a fine unmelted mass. Similarly, there is a problem that it cannot be applied as a surface protective film.
JP-A-9-111208 JP 54-133578 A JP 2006-282761 A

  In view of the problems of the prior art described above, the present invention has very little fish eye, excellent blocking properties without using an anti-blocking agent, excellent transparency, and improved peel force control and feeding performance. Further, it is made of a propylene-based resin suitable as a film for protecting a surface of a building member such as a synthetic resin plate, a decorative plate, a metal plate, or a glass plate, and as a surface protecting film for a liquid crystal display component such as a polarizing plate or a retardation plate. It aims at providing the film for surface protection.

  As a result of repeating various studies to solve the above problems, the present inventor used a propylene-ethylene block copolymer having a tan δ curve obtained by a specific production method, MFR, and solid viscoelasticity measurement as a base material layer. Self-adhesive surface protection made of propylene resin with less fish eye and transparency by using acrylic adhesive for adhesive layer and silicone or long-chain alkyl release agent for release layer The present invention was completed by finding that a film for use was obtained.

That is, according to the first aspect of the present invention, in the surface protective film in which the adhesive layer is formed on one surface of the base material layer and the release treatment layer is formed on the other surface, the base material layer is a metallocene catalyst. Is formed from a propylene-ethylene block copolymer (A) having the following characteristics (a1) to (a3), the adhesive layer is formed from an acrylic adhesive (B), and the release treatment layer is silicone. When the release treatment layer is formed by applying a silicone-type or long-chain alkyl release agent (C) in a subsequent step, the release treatment agent is formed with a system or long-chain alkyl release agent (C). A coating film for surface protection is provided, wherein the coating amount of (C) is 10 g / m ² or less .
(A) Propylene-ethylene block copolymer (a1) Using a metallocene-based catalyst, 30 to 95% by weight of propylene alone or propylene-ethylene random copolymer component (A1) in the first step, component in the second step Propylene-ethylene block copolymer (a2) obtained by sequential polymerization of 70 to 5% by weight of propylene-ethylene random copolymer component (A2) containing more ethylene than (A1) Melt flow rate (MFR: 230 ° C. 2.16 kg) is 1-30 g / 10 min. (A3) In the temperature-loss tangent (tan δ) curve obtained by solid viscoelasticity measurement (DMA), the tan δ curve has a single peak at 0 ° C. or lower.

According to a second aspect of the present invention, there is provided a surface protective film characterized in that, in the first aspect, the propylene-ethylene block copolymer (A) further satisfies the following (a4). The
(A4) The component amount W (Mw ≦ 5,000) having a molecular weight of 5,000 or less obtained by gel permeation chromatography (GPC) is 0.8% by weight or less of the total.

According to the third aspect of the present invention, in the first or second aspect, the propylene-ethylene block copolymer (A) further satisfies the following (a5) to (a6): A protective film is provided.
(A5) The component (A1) obtained in the first step is a propylene-ethylene random copolymer having an ethylene content in the range of 0.5 to 6% by weight, and the proportion of the entire block copolymer is 30 to 85. In the range of% by weight, the component (A2) obtained in the second step has an ethylene content of 6 to 15% by weight more than (A1), and the ratio of the whole block copolymer is 70 to 15% by weight. (A6) It is obtained as a plot of the elution amount (dWt% / dT) against temperature by the temperature rising elution fractionation method (TREF) in the temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent. In the TREF elution curve, the peak temperature T (A1) observed on the high temperature side is in the range of 55 ° C. to 96 ° C., and the peak temperature T (A2) observed on the low temperature side is 45 ° C. or lower, or Over peak temperature T (A2) is not observed, propylene - the temperature T to 99 wt% of the ethylene block copolymer is eluted (A4) is 98 ° C. or less

According to the fourth invention of the present invention, in any one of the first to third inventions, the propylene-ethylene block copolymer (A) further satisfies the following (a7) to (a8). A surface protective film is provided.
(A7) The component (A1) obtained in the first step is a propylene-ethylene random copolymer having an ethylene content in the range of 1.5 to 6% by weight, and the proportion of the whole block copolymer is 30 to 70. In the range of% by weight, the component (A2) obtained in the second step has an ethylene content of 8 to 15% by weight more than (A1), and the ratio of the whole block copolymer is in the range of 70 to 30% (A8) It is obtained as a plot of the elution amount (dWt% / dT) against temperature by the temperature rising elution fractionation method (TREF) in the temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent. In the TREF elution curve, the peak temperature T (A1) observed on the high temperature side is in the range of 60 ° C. to 88 ° C., and the peak temperature T (A2) observed on the low temperature side is 40 ° C. or lower, or Over peak temperature T (A2) is not observed, propylene - the temperature T to 99 wt% of the ethylene block copolymer is eluted (A4) is 90 ° C. or less

According to a fifth aspect of the present invention, in any one of the first to fourth aspects, the propylene-ethylene block copolymer (A) further satisfies the following (a9): Films are provided.
(A9) Intrinsic viscosity [η] cxs measured in 135 ° C. decalin of 23 ° C. xylene solubles is 1 to 2 dl / g

  Moreover, according to the sixth invention of the present invention, in any one of the first to fifth inventions, it is used for surface protection of building members such as a synthetic resin plate, a decorative plate, a metal plate, and a glass plate. A surface protective film is provided.

  According to a seventh aspect of the present invention, in any one of the first to fifth aspects, the surface is used for protecting a surface of a liquid crystal display component such as a polarizing plate or a retardation plate. A protective film is provided.

  The propylene-based surface protective film of the present invention is obtained by using a specific propylene-ethylene block copolymer polymerized using a metallocene catalyst for a base material layer and an acrylic pressure-sensitive adhesive for the pressure-sensitive adhesive layer. When at least one of the layer and the pressure-sensitive adhesive layer is laminated in a molten state, it adheres firmly and has excellent delamination, so that there are very few unmelted fish eyes at the time of film formation, and the pressure-sensitive adhesive layer and the base material layer There is no risk of delamination and yet exhibits excellent tackiness. For this reason, even if a surface protection film is affixed on a to-be-protected object and stored in a stacked manner, the to-be-protected object does not dent. Moreover, the film for surface protection of this invention is excellent in blocking property without using an antiblocking agent, and is excellent in transparency. Furthermore, since a silicone-based or long-chain alkyl-based release treatment agent is used for the release treatment layer as the release treatment layer, when the roll is unwound from the roll winding state where both the adhesive layer and the release treatment layer are in contact with each other in a solid state, It can be made into a film for surface protection having the property that peeling and improving the drawability during use.

  The present invention relates to a propylene-based surface protective film having an adhesive layer formed on one surface of a base material layer and having a release treatment layer on the opposite surface of the adhesive layer, and the base material layer is polymerized using a metallocene catalyst. And the characteristics (a1) to (a3) and, if necessary, the propylene-ethylene block copolymer (A) further having characteristics (a4) to (a9), and the pressure-sensitive adhesive layer is an acrylic pressure-sensitive adhesive And a release treatment layer is formed of a silicone-type or long-chain alkyl-type release treatment agent (C). Hereinafter, the component of each layer of the film for surface protection of this invention and the manufacturing method of the film for surface protection are demonstrated in detail.

1. Base material layer The following propylene-ethylene block copolymer (A) is used for the base material layer and the adhesion layer in the film for surface protection of this invention.

  The propylene-ethylene block copolymer (A) used in the present invention is a propylene homopolymer or a propylene-ethylene random copolymer component (A1) (hereinafter sometimes referred to as component (A1)) and propylene-. It is composed of an ethylene random copolymer component (A2) (hereinafter sometimes referred to as component (A2)), and the following properties (a1) to (a3) and, if necessary, properties (a4) to (a9) It satisfies.

(A1) Using a metallocene-based catalyst, 30 to 95% by weight of propylene homopolymer or propylene-ethylene random copolymer component (A1) in the first step, and more ethylene than component (A1) in the second step Propylene-ethylene block copolymer obtained by sequentially polymerizing 70 to 5% by weight of the propylene-ethylene random copolymer component (A2). Such propylene-ethylene block copolymer (A) is a so-called block. Although it is commonly referred to as a copolymer, it is in a blended state of component (A1) and component (A2), and both are not bonded by polymerization.
(A2) Melt flow rate (MFR: 230 ° C. 2.16 kg) is 1 to 30 g / 10 minutes (a3) Temperature-loss tangent (tan δ) curve obtained by solid viscoelasticity measurement (DMA), tan δ curve is 0 ° C. The component amount W (Mw ≦ 5,000) having a molecular weight of 5,000 or less obtained by gel permeation chromatography (GPC) measurement having a single peak below is 0.8% by weight or less (Mw ≦ 5,000) ( a5) The component (A1) obtained in the first step is a propylene-ethylene random copolymer having an ethylene content in the range of 0.5 to 6% by weight, and the proportion of the block copolymer as a whole is 30 to 85% by weight. %, The component (A2) obtained in the second step has an ethylene content of 6 to 15% by weight more than (A1), and the proportion of the whole block copolymer is (A6) Elution amount with respect to temperature (dWt% /%) by temperature rising elution fractionation method (TREF) in a temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent. In the TREF elution curve obtained as a plot of dT), the peak temperature T (A1) observed on the high temperature side is in the range of 55 ° C. to 96 ° C., and the peak temperature T (A2) observed on the low temperature side is 45 ° C. Or the peak temperature T (A2) is not observed and the temperature T (A4) at which 99 wt% of the propylene-ethylene block copolymer elutes is 98 ° C. or less (a7) obtained in the first step. Component (A1) is a propylene-ethylene random copolymer having an ethylene content in the range of 1.5 to 6% by weight, and the proportion of the block copolymer in the whole is in the range of 30 to 70% by weight. The component (A2) obtained in the second step has an ethylene content of 8 to 15% by weight more than (A1), and the ratio of the entire block copolymer is in the range of 70 to 30% by weight ( a8) In a TREF elution curve obtained as a plot of elution amount (dWt% / dT) against temperature by a temperature rising elution fractionation method (TREF) in a temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent The peak temperature T (A1) observed on the high temperature side is in the range of 60 ° C. to 88 ° C., the peak temperature T (A2) observed on the low temperature side is 40 ° C. or lower, or the peak temperature T (A2) Is not observed, and the temperature T (A4) at which 99 wt% of the propylene-ethylene block copolymer elutes is 90 ° C. or less (a9) measured in 135 ° C. decalin that is soluble in 23 ° C. xylene. Intrinsic viscosity [eta] cxs is 1~2dl / g
Hereinafter, the characteristics (a1) to (a9) will be described in detail.

(1) Ethylene content in component (A1) ([E] _A1 )
The component (A1) produced in the first step suppresses stickiness of the film and exhibits heat resistance, so that the propylene homopolymer or propylene-ethylene random copolymer having a relatively high melting point and crystallinity. Must be coalesced. [E] _A1 preferably has an ethylene content ([E] _A1 ) of 7% by weight or less, more preferably 6% by weight or less, and further preferably 0.5 to 6% by weight. [E] When _A1 exceeds 7% by weight, the melting point becomes too low and the heat resistance of the film may be deteriorated.
Component (A1) exhibits improved transparency and heat resistance even with a propylene homopolymer, but when component (A1) is a propylene homopolymer, it exhibits sufficient flexibility while maintaining transparency. Therefore, it is necessary to extremely increase the proportion of the component (A2) to be described later, which may cause remarkable deterioration such as heat resistance, stickiness and blocking.
On the other hand, when the component (A1) is a propylene-ethylene random copolymer, the heat resistance seems to deteriorate due to a decrease in the melting point of the component (A1) itself, but it is necessary for exhibiting sufficient flexibility. Since the amount of the component (A2) can be suppressed, the heat resistance of the block copolymer as a whole is rather improved, and stickiness and blocking are less deteriorated, which is preferable.
Further, by reducing the melting point, it is possible to obtain a film excellent in odor and the like because sufficient extrusion stability and the like can be obtained even if the molding temperature during film molding is lowered.
From these viewpoints, the ethylene content in the component (A1) is preferably 0.5% by weight or more, more preferably 1.5% by weight or more.

(2) Ethylene content in component (A2) ([E] _A2 )
The propylene-ethylene random copolymer component (A2) produced in the second step is a component necessary for improving the flexibility, impact resistance and transparency of the propylene-ethylene block copolymer (A). .
Here, the component (A2) needs to have an ethylene content in a specific range in order to sufficiently exhibit the above effects. That is, in the block copolymer of the present invention, the lower the crystallinity of the component (A2) relative to the component (A1), the greater the flexibility improvement effect, and the crystallinity is the ethylene content in the propylene-ethylene random copolymer. Therefore, the ethylene content [E] _A2 in the component (A2) is preferably 3% by weight or more, more preferably 6% by weight, more than the ethylene content [E] _A1 E in the component (A1). As mentioned above, More preferably, it contains 8 weight% or more ethylene more than a component (A1).
Here, when the difference in ethylene content between the component (A1) and the component (A2) is defined as [E] gap ([E] _A2− [E] _A1 ), [E] gap is in the range of 3 to 20% by weight. More preferably, it is 6 to 15 weight%, More preferably, it is 8 to 15 weight%.
[E] If the gap is less than 3% by weight, the rubber elasticity is insufficient, which is not preferable. On the other hand, if it exceeds 20% by weight, a phase separation structure divided into a matrix and a domain of the component (A1) and the component (A2) produced in the first step is taken and the compatibility is deteriorated, so that the transparency is lowered. This is because polypropylene originally has low compatibility with polyethylene, and even in the case of propylene-ethylene random copolymers, although the ethylene content is different, the compatibility with each other decreases as the difference in ethylene content increases. is there.

(3) Ratio of component (A1) and component (A2) Ratio of component (A1) constituting propylene-ethylene block copolymer (W (A1)) and ratio of component (A2) (W (A2)) The content ratio should be such that W (A1) is 30 to 95% by weight and W (A2) is in the range of 70 to 5% by weight, and preferably the ratio of W (A1) is 30 to 85% by weight. %, More preferably in the range of 50 to 80% by weight.
If the ratio of W (A1) is less than 30% by weight, stickiness of the film may occur and heat resistance may be reduced. On the other hand, when the ratio of W (A1) exceeds 95% by weight, the effect of improving the flexibility, impact resistance and transparency of the propylene-ethylene block copolymer cannot be sufficiently exhibited.
When the proportion of the component (A2) is too large, the stickiness increases, the blocking is deteriorated, and the heat resistance is significantly reduced. On the other hand, if the proportion of the component (A2) is too small, the effect of improving flexibility and impact resistance cannot be obtained.

(4) Measurement of _{[E] A1} and _[E] measured in _A2 and W (A1) and W (A2) _{[E] A1} and _{[E] A2} and W (A1) and W (A2) is, at the time of manufacture Although it is possible to specify by the material balance (material balance), in order to specify these more accurately, it is desirable to use the following analysis.
(I) Identification of W (A1) and W (A2) by temperature-temperature elution fractionation (TREF) The technique for evaluating the crystallinity distribution of a propylene-ethylene random copolymer by TREF is well known to those skilled in the art. Yes, for example, detailed measurement methods are shown in the following documents.
G. Glockner, J. et al. Appl. Polym. Sci. : Appl. Polym. Symp. 45, 1-24 (1990)
L. Wild, Adv. Polym. Sci. 98, 1-47 (1990)
J. et al. B. P. Soares, A .; E. Hamielec, Polymer; 36,
8, 1639-1654 (1995)

  The propylene-ethylene block copolymer in the present invention is greatly different in the crystallinity of each of the components (A1) and (A2), and each crystallinity distribution is narrow by being produced using a metallocene catalyst. Therefore, there are very few intermediate components between the two, and both can be discriminated with high accuracy by TREF.

A specific method will be described with reference to the figure showing the elution amount and the elution amount integration by TREF in FIG. In the TREF elution curve (plot of elution amount with respect to temperature), components (A1) and (A2) show their elution peaks at T (A1) and T (A2) due to the difference in crystallinity, and the difference is sufficiently large. Separation is possible at an intermediate temperature T (C) (= {T (A1) + T (A2)} / 2).
In addition, the lower limit of the TREF measurement temperature is −15 ° C. in the apparatus used for this measurement, but in the case where the crystallinity of the component (A2) is very low or an amorphous component, There may be no peak in the range. (In this case, the concentration of the component (A2) dissolved in the solvent is detected at the measurement temperature lower limit (ie, −15 ° C.).)
At this time, T (A2) is considered to exist below the lower limit of the measurement temperature, but the value cannot be measured. In such a case, T (A2) is the lower limit of the measurement temperature. Defined as ° C.
Here, if the integrated amount of the component eluting up to T (C) is defined as W (A2) wt%, and the integrated amount of the portion eluting at T (C) or higher is defined as W (A1) wt%, W (A2) Almost corresponds to the amount of the component (A2) having low crystallinity or non-crystallinity, and the integrated amount W (A1) of the component eluted at T (C) or higher is the component (A1) having relatively high crystallinity. Almost corresponds to the amount of. The elution amount curve obtained by TREF and the above-described methods for calculating the various temperatures and amounts obtained therefrom are performed as illustrated in FIG.

(Ii) Method for measuring TREF In the present invention, TREF is specifically measured as follows.
A sample is dissolved in o-dichlorobenzene (containing 0.5 mg / mL BHT) at 140 ° C. to prepare a solution. This is introduced into a 140 ° C. TREF column, cooled to 100 ° C. at a rate of 8 ° C./min, subsequently cooled to −15 ° C. at a rate of 4 ° C./min, and held for 60 minutes. Thereafter, o-dichlorobenzene (containing 0.5 mg / mL BHT) as a solvent is flowed through the column at a flow rate of 1 mL / min, and components dissolved in o-dichlorobenzene at −15 ° C. are eluted in the TREF column for 10 minutes. Next, the column is linearly heated to 140 ° C. at a heating rate of 100 ° C./hour to obtain an elution curve.

(Iii) Specificity of ethylene content [E] _A1 and [E] _A2 in each component (a) Separation of component (A1) and component (A2) Based on T (C) determined by the above TREF measurement, Using a temperature-separating column separation method using a preparative type separation apparatus, the soluble component (A2) in T (C) and the insoluble component (A1) in T (C) are separated, and the ethylene content of each component is determined by NMR. .
The temperature rising column fractionation method refers to a measurement method disclosed in, for example, Macromolecules, 21 314 to 319 (1988). Specifically, the following method is used in the present invention.
(B) Fractionation conditions A cylindrical column having a diameter of 50 mm and a height of 500 mm is filled with a glass bead carrier (80 to 100 mesh) and maintained at 140 ° C. Next, 200 mL of the o-dichlorobenzene solution (10 mg / mL) of the sample dissolved at 140 ° C. is introduced into the column. Thereafter, the temperature of the column is cooled to 0 ° C. at a rate of temperature decrease of 10 ° C./hour. After holding at 0 ° C. for 1 hour, the column temperature is heated to T (C) at a heating rate of 10 ° C./hour and held for 1 hour. Note that the temperature control accuracy of the column through a series of operations is ± 1 ° C.
Next, while maintaining the column temperature at T (C), 800 mL of o (dichlorobenzene) of T (C) is allowed to flow at a flow rate of 20 mL / min, whereby components soluble in T (C) existing in the column are obtained. Elute and collect.
Next, the column temperature is increased to 140 ° C. at a temperature rising rate of 10 ° C./min, and after leaving still at 140 ° C. for 1 hour, by flowing 800 mL of a 140 ° C. solvent (o-dichlorobenzene) at a flow rate of 20 mL / min, Elute insoluble components with T (C) and collect.
The solution containing the polymer obtained by fractionation is concentrated to 20 mL using an evaporator and then precipitated in 5 times the amount of methanol. The precipitated polymer is recovered by filtration and then dried overnight in a vacuum dryer.
^(C) 13 C-NMR according to the measurement the fractionated by components obtained ethylene content ^{(A1) (A2) 13 C} -NMR spectrum ethylene content was determined according to the following conditions by complete proton decoupling method for each It is obtained by analyzing.
Model: GSX-400 manufactured by JEOL Ltd. or equivalent equipment (carbon nuclear resonance frequency of 100 MHz or more)
Solvent: o-dichlorobenzene / heavy benzene = 4/1 (volume ratio)
Concentration: 100 mg / mL
Temperature: 130 ° C
Pulse angle: 90 °
Pulse interval: 15 seconds Integration count: 5,000 times or more The attribution of the spectrum may be performed with reference to, for example, Macromolecules, 17 1950 (1984).
The spectrum assignments measured under the above conditions are as shown in Table 1 below. In Table 1, symbols such as S _αα are in accordance with the notation of Carman et al. (Macromolecules, 10 536 (1977)), P represents a methyl carbon, S represents a methylene carbon, and T represents a methine carbon.

Hereinafter, when “P” is a propylene unit in a copolymer chain and “E” is an ethylene unit, six kinds of triads of PPP, PPE, EPE, PEP, PEE, and EEE may exist in the chain. As described in Macromolecules, 15 1150 (1982), the concentration of these triads and the peak intensity of the spectrum are linked by the following relational expressions (1) to (6).
[PPP] = k × I (T _ββ ) (1)
[PPE] = k × I (T _βδ ) (2)
[EPE] = k × I (T _δδ ) (3)
[PEP] = k × I (S _ββ ) (4)
[PEE] = k × I (S _βδ ) (5)
[EEE] = k × {I (S _δδ ) / 2 + I (S _γδ ) / 4} (6)
Here, [] indicates the fraction of triads, for example, [PPP] is the fraction of PPP triads in all triads. Therefore,
[PPP] + [PPE] + [EPE] + [PEP] + [PEE] + [EEE] = 1
... (7)
It is.
Further, k is a constant, I indicates the spectral intensity, and for example, I (T _ββ ) means the intensity of the peak at 28.7 ppm attributed to T _ββ .

By using the relational expressions of the above formulas (1) to (7), the fraction of each triad is obtained, and the ethylene content is obtained by the following formula.
Ethylene content (mol%) = ([PEP] + [PEE] + [EEE]) × 100

  In addition, the propylene random copolymer of the present invention contains a small amount of a propylene hetero bond (2,1-bond and / or 1,3-bond), thereby producing the following minute peak.

In order to obtain an accurate ethylene content, it is necessary to include these peaks derived from heterogeneous bonds in the calculation, but it is difficult to completely separate and identify the peaks derived from heterogeneous bonds, and the amount of heterogeneous bonds is small Therefore, the ethylene content of the present invention is obtained by using the relational expressions (1) to (7) in the same manner as the analysis of the copolymer produced with a Ziegler catalyst that does not substantially contain a heterogeneous bond. To do.
Conversion from mol% to wt% of ethylene content is carried out using the following formula: ethylene content (wt%) = (28 × X / 100) / {28 × X / 100 + 42 × (1−X / 100) } × 100
Here, X is the ethylene content in mol%.

The ethylene content [E] _W of the entire propylene-ethylene block copolymer is calculated from the respective ethylene contents [E] _A1 , [E] _A2 and TREF measured from the components (A1) and (A2). From the weight ratios W (A1) and W (A2)% by weight of the respective components, the following formula is used.
[E] _W = {[E] _A1 × W (A1) + [E] _A2 × W (A2) / 100 (% by weight)

(4) Melt flow rate (MFR) of block copolymer (A)
The melt flow rate (MFR) of the propylene-ethylene block copolymer used in the present invention is 1 to 30 g / 10 minutes, preferably 4 to 15 g / 10 minutes. When the MFR is less than 1 g / 10 min, surface roughness called shark skin or melt fracture occurs on the surface of the film, and the transparency and appearance are significantly impaired. On the other hand, if the MFR is too high, the stability during molding deteriorates, the width and thickness of the film fluctuate, and a product cannot be obtained.
Here, MFR is a value measured at a heating temperature of 230 ° C. and a load of 21.18 N in accordance with JIS K7210 A method condition M.

(5) Definition by peak of tan δ curve In the present invention, in order to maintain good compatibility of the film, the component (A1) and the component (A2) constituting the propylene-ethylene block copolymer to be used are phase separated. It is necessary not to do. The phase separation conditions are affected not only by the ethylene content but also by the molecular weight and composition. Therefore, in addition to the above-mentioned regulations regarding the ethylene content, a temperature-loss tangent (tan δ) curve obtained by solid viscoelasticity measurement (DMA) Therefore, it is necessary to define the peak of the tan δ curve.
In the propylene-ethylene block copolymer (A) used in the present invention, in the temperature-loss tangent (tan δ) curve obtained by solid viscoelasticity measurement (DMA), the tan δ curve has a single peak at 0 ° C. or lower. It is necessary to have.
When the propylene-ethylene block copolymer (A) has a phase separation structure, the glass transition temperature of the amorphous part contained in the component (A1) and the glass transition temperature of the amorphous part contained in the component (A2) are Since each is different, there are a plurality of peaks. In this case, there arises a problem that the transparency is remarkably deteriorated.
Whether or not the phase separation structure is taken can be discriminated in the tan δ curve in the measurement of solid viscoelasticity. Is brought about by having.

  Specifically, solid viscoelasticity measurement is performed by applying a sinusoidal strain of a specific frequency to a strip-shaped sample piece and detecting the generated stress. Here, the frequency is 1 Hz and the measurement temperature is raised stepwise from −60 ° C. until the sample is melted and cannot be measured. Further, it is recommended that the magnitude of distortion is about 0.1 to 0.5%. From the obtained stress, the storage elastic modulus G ′ and the loss elastic modulus G ″ are obtained by a known method, and the loss tangent (= loss elastic modulus / storage elastic modulus) defined by this ratio is plotted against the temperature. It shows a sharp peak in the temperature range below 0 ° C. Generally, the peak of the tan δ curve below 0 ° C. is for observing the glass transition of the amorphous part, and here the peak temperature is defined as the glass transition temperature Tg (° C.). Define.

(6) Molecular weight The amount of the component having a weight average molecular weight of 5,000 or less as measured by the gel permeation (GPC) method of the propylene-ethylene block copolymer used in the present invention is preferably 0.8% by weight or less. More preferably, it is 0.5 wt% or less. The propylene-ethylene block copolymer (A) in the present invention has an additional feature that the low molecular weight component is small, and the low molecular weight component, particularly the component whose molecular weight is less than the entangled molecular weight, It seems to bleed out on the surface and deteriorate stickiness and transparency.
In addition, the molecular weight between the entanglement points of polypropylene is about 5,000 as described in Journal of Polymer Science: Part B: Polymer Physics; 37 1023-1103 (1999).

Here, the weight average molecular weight (Mw) refers to that measured by gel permeation chromatography (GPC).
Conversion from the retention volume to the molecular weight is performed using a calibration curve prepared in advance with standard polystyrene.
Standard polystyrenes used are the following brands manufactured by Tosoh Corporation. F380, F288, F128, F80, F40, F20, F10, F4, F1, A5000, A2500, A1000
A calibration curve is prepared by injecting 0.2 ml of a solution dissolved in o-dichlorobenzene (containing 0.5 mg / ml BHT) so that each is 0.5 mg / ml.
The calibration curve uses a cubic equation obtained by approximation by the least square method. The following numerical value is used for [η] = K × M ^α in the viscosity formula used for conversion to molecular weight.
PS: K = 1.38 × 10 ⁻⁴ α = 0.7
PE: K = 3.92 × 10 ⁻⁴ α = 0.733
PP: K = 1.03 × 10 ⁻⁴ α = 0.78
The measurement conditions for GPC are as follows.
Apparatus: GPC (ALC / GPC 150C) manufactured by WATERS
Detector: MIRAN 1A IR detector (measured wavelength: 3.42 μm) manufactured by FOXBORO
Column: AD806M / S (3 pieces) manufactured by Showa Denko KK
Mobile phase solvent: o-dichlorobenzene Measurement temperature: 140 ° C.
Flow rate: 1.0 ml / min
Injection volume: 0.2ml
Sample Preparation Prepare a 1 mg / ml solution using o-dichlorobenzene (containing 0.5 mg / ml BHT) and dissolve it at 140 ° C. for about 1 hour.
The amount of the component having a molecular weight of 5,000 or less can also be determined from a plot of the elution ratio with respect to the molecular weight obtained by GPC measurement.

(7) Intrinsic viscosity [η] cxs
In the propylene-ethylene block copolymer (A), it is a component (CXS component) that is soluble in xylene at room temperature, in which stickiness and bleed out are particularly problematic. Therefore, the measurement of intrinsic viscosity [η] cxs is: It is preferable to carry out for the CXS component.
Here, the CXS component was prepared by dissolving the propylene-ethylene block copolymer (A) in p-xylene at 130 ° C. to form a solution, and then leaving the solution at 25 ° C. for 12 hours. The intrinsic viscosity [η] cxs of the CXS component obtained by evaporating p-xylene can be measured by using an Ubbelohde viscometer at a temperature of 135 ° C. using decalin as a solvent.
At this time, since the propylene-ethylene block copolymer (A) of the present invention does not increase the generation of a component having a molecular weight of 5,000 or less that tends to bleed out, the conventional Ziegler-Natta catalyst is Even if the intrinsic viscosity [η] cxs of the CXS component is in the region of 2 or less, which has been a practical problem due to problems such as blocking and deterioration of blocking, it can be produced and used without causing any particular deterioration in physical properties. it can.
The propylene-ethylene block copolymer which does not increase the component having a molecular weight of 5,000 or less while lowering the intrinsic viscosity of such a CXS component has characteristics in terms of physical properties such as high tensile elongation at break and high tensile strength at break. In addition, there is an effect that there is little occurrence of an appearance defect called “butsu” or “fish eye”.

(8) Additional requirements for crystallinity distribution by TREF elution curve By using the TREF elution curve used to specify the amount of each component, it was added to the propylene-ethylene block copolymer of the present invention in the crystallinity distribution. Characteristic can be found.
(I) Elution peak temperature T (A1)
The higher the elution peak temperature T (A1) of the component (A1) in the TREF elution curve, the higher the crystallinity of the component (A1). At this time, the higher the crystallinity of the component (A1), the higher the propylene-ethylene block content. The component (A2) necessary for improving the adhesiveness and transparency of the polymer (A) must be increased.
On the other hand, if the proportion of the component (A2) is too large, stickiness and heat resistance are deteriorated. Therefore, in order to improve the balance between adhesiveness and transparency, T (A1) should not be too high. Further, odor properties and the like tend to deteriorate with an increase in molding temperature, but it is also preferable in that stable plasticization can be obtained by reducing T (A1) even if the extrusion temperature is lowered.
In the present invention, the component (A1) is propylene alone or a propylene / ethylene random copolymer, but T (A1) can be decreased by increasing the ethylene content. At this time, in order to exhibit a sufficient balance between adhesiveness, transparency and heat resistance, T (A1) is preferably 96 ° C. or lower, and the most preferable range is preferably 88 ° C. or lower.
On the other hand, when the peak temperature T (A1) is less than 55 ° C., the temperature at which the component (A1) crystals melt is low, and the block copolymer cannot exhibit sufficient heat resistance, resulting in poor blocking. Therefore, in the present invention, the peak temperature T (A1) is preferably 55 ° C. or higher, and more preferably 60 ° C. or higher.

(Ii) Elution end temperature T (A4)
Even if T (A1) is low, transparency is deteriorated when the crystallinity distribution is present on the high crystal side. The cause of this is not clear, but if there is a crystalline distribution on the high crystal side, the density of the crystal structure increases and the density difference from the amorphous part increases, or the nucleation frequency decreases and the spherulite size increases. This is probably because of this.
Therefore, it is preferable that the crystallinity spread to the high temperature side is suppressed in the TREF elution curve. The spread of crystallinity toward the high crystal side can be evaluated by TREF measurement, and the elution end temperature T (A4) of the entire component propylene-ethylene block copolymer (A) with respect to the peak temperature T (A1) (however, Considering errors in TREF measurement, it is difficult to define the temperature at which all elution occurs. Therefore, in the present invention, it is preferable that the temperature at which 99 wt% of the total elution is defined as the elution end temperature T (A4)) is not high. If there is an elution component on the high temperature side, the crystallinity of the component increases. Therefore, as a preferable requirement of the present invention, T (A4) is 98 ° C. or less, preferably 90 ° C. or less.
Furthermore, the temperature difference ΔT (T (A4) −T (A1)) from the elution peak to the end is preferably 5 ° C. or less, more preferably 4 ° C. or less, and even more preferably 3 ° C. or less.

(Iii) Elution peak temperature T (A2)
Since the adhesiveness and transparency of the propylene-ethylene block copolymer (A) cannot be ensured unless the crystallinity of the component (A2) is sufficiently lowered, T (A2) is preferably 45 ° C. or less. More preferably, it is 40 degrees C or less.

(9) Production of propylene-ethylene block copolymer (A) The method for producing the propylene-ethylene block copolymer (A) of the present invention requires the use of a metallocene catalyst. It is well known to those skilled in the art that stickiness and bleedout deteriorate when the molecular weight and crystallinity distribution are wide in the propylene-ethylene block copolymer, but also in the propylene-ethylene block copolymer used in the present invention, In order to suppress stickiness and bleed out and to exhibit sufficient transparency in film forming, it is necessary to polymerize using a metallocene-based catalyst capable of narrowing the molecular weight and crystallinity distribution. The fact that the excellent propylene-ethylene block copolymer of the present invention cannot be obtained with the system catalyst is also apparent from the comparison of Examples and Comparative Examples described later.

Here, the type of the metallocene-based catalyst is not particularly limited as long as a copolymer having the performance of the present invention can be produced, but in order to satisfy the requirements of the present invention, for example, as shown below: It is preferable to use a metallocene-based catalyst comprising the component (x), the component (y), and the component (z) used as necessary.
Component (x): At least one metallocene transition metal compound selected from the transition metal compounds represented by the general formula (1) Component (y): At least one selected from the following (y-1) to (y-4) Ionic compound capable of reacting with solid component (y-1), particulate carrier (y-2) component (x) on which solid organic component (y-1) is supported, and converting component (x) into a cation Fine carrier on which Lewis acid is supported (y-3) Solid acid fine particle (y-4) Ion exchange layered silicate component (z): Organoaluminum compound

Ingredient (x)
As the component (x), at least one metallocene transition metal compound selected from transition metal compounds represented by the following general formula (1) can be used.
^{_{Q (C 5 H 4-a}} -aR 1) (C 5 H 4-b -bR 2) MeXY ... (1)
[Wherein Q represents a divalent linking group that bridges two conjugated five-membered ring ligands, Me represents a metal atom selected from titanium, zirconium, and hafnium, and X and Y represent hydrogen atoms. Atom, halogen atom, hydrocarbon group, alkoxy group, amino group, nitrogen-containing hydrocarbon group, phosphorus-containing hydrocarbon group or silicon-containing hydrocarbon group, X and Y are each independently, ie, the same or different. Also good. R ¹ and R ² represent hydrogen, a hydrocarbon group, a halogenated hydrocarbon group, a silicon-containing hydrocarbon group, a nitrogen-containing hydrocarbon group, an oxygen-containing hydrocarbon group, a boron-containing hydrocarbon group, or a phosphorus-containing hydrocarbon group. . a and b are the number of substituents. ]

Specifically, Q represents a divalent linking group that bridges two conjugated five-membered ring ligands. For example, a divalent hydrocarbon group, a silylene group, an oligosilylene group, or a hydrocarbon group as a substituent. Examples thereof include a silylene group, an oligosilylene group, or a germylene group having a hydrocarbon group as a substituent. Among these, preferred is a silylene group having a divalent hydrocarbon group and a hydrocarbon group as a substituent.
X and Y represent a hydrogen atom, a halogen atom, a hydrocarbon group, an alkoxy group, an amino group, a nitrogen-containing hydrocarbon group, a phosphorus-containing hydrocarbon group, or a silicon-containing hydrocarbon group. Among these, hydrogen is preferable , Chlorine, methyl, isobutyl, phenyl, dimethylamide, diethylamide group and the like. X and Y may be independent, that is, may be the same or different.
R ¹ and R ² represent hydrogen, a hydrocarbon group, a halogenated hydrocarbon group, a silicon-containing hydrocarbon group, a nitrogen-containing hydrocarbon group, an oxygen-containing hydrocarbon group, a boron-containing hydrocarbon group, or a phosphorus-containing hydrocarbon group. . Specific examples of the hydrocarbon group include a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group, an octyl group, a phenyl group, a naphthyl group, a butenyl group, and a butadienyl group. In addition, halogenated hydrocarbon group, silicon-containing hydrocarbon group, nitrogen-containing hydrocarbon group, oxygen-containing hydrocarbon group, boron-containing hydrocarbon group or phosphorus-containing hydrocarbon group include methoxy group, ethoxy group, phenoxy group, trimethylsilyl group. Typical examples include a group, diethylamino group, diphenylamino group, pyrazolyl group, indolyl group, dimethylphosphino group, diphenylphosphino group, diphenylboron group, dimethoxyboron group and the like. In these, it is preferable that it is a C1-C20 hydrocarbon group, and it is especially preferable that they are a methyl group, an ethyl group, a propyl group, and a butyl group. By the way, adjacent R ¹ and R ² may combine to form a ring, on which a hydrocarbon group, halogenated hydrocarbon group, silicon-containing hydrocarbon group, nitrogen-containing hydrocarbon group, oxygen-containing You may have a substituent which consists of a hydrocarbon group, a boron containing hydrocarbon group, or a phosphorus containing hydrocarbon group.
Me is a metal atom selected from titanium, zirconium and hafnium, preferably zirconium and hafnium.

  Among the components (x) described above, preferred for the production of the propylene polymer of the present invention is a substituted cyclopentadienyl group crosslinked with a silylene group, a germylene group or an alkylene group having a hydrocarbon substituent. A transition metal compound comprising a ligand having a substituted indenyl group, a substituted fluorenyl group or a substituted azulenyl group, particularly preferably a 2,4-position crosslinked with a silylene group having a hydrocarbon substituent or a germylene group It is a transition metal compound comprising a ligand having a substituted indenyl group and a 2,4-position substituted azulenyl group.

Non-limiting specific examples include dimethylsilylene bis (2-methyl-4-phenylindenyl) zirconium dichloride, diphenylsilylene bis (2-methyl-4-phenylindenyl) zirconium dichloride, dimethylsilylene bis (2-methyl). Benzoindenyl) zirconium dichloride, dimethylsilylene bis {2-isopropyl-4- (3,5-diisopropylphenyl) indenyl} zirconium dichloride, dimethylsilylene bis (2-propyl-4-phenanthrylindenyl) zirconium dichloride, dimethyl Silylene bis (2-methyl-4-phenylazurenyl) zirconium dichloride, dimethylsilylene bis {2-methyl-4- (4-chlorophenyl) azurenyl} zirconium dichloride, dimethylsilylene bi (2-Ethyl-4-phenylazurenyl) zirconium dichloride, dimethylsilylenebis (2-isopropyl-4-phenylazurenyl) zirconium dichloride, dimethylsilylenebis {2-ethyl-4- (2-fluorobiphenyl) azurenyl} zirconium Dichloride, dimethylsilylenebis {2-ethyl-4- (4-t-butyl-3-chlorophenyl) azurenyl} zirconium dichloride, and the like can be given.
A compound in which the silylene group of these specific examples is replaced with a germylene group and zirconium is replaced with hafnium is also exemplified as a suitable compound. In addition, since the catalyst component is not an important element of the present invention, it avoids complicated listing and is limited to a representative example, but it is obvious that the effective range of the present invention is not limited thereby. It is.

Ingredient (y)
As the component (y), at least one solid component selected from the components (y-1) to (y-4) described above is used. Each of these components is a known component, and can be appropriately selected from known technologies and used. Specific examples and manufacturing methods thereof are described in detail in JP-A No. 2002-284808, JP-A No. 2002-53609, JP-A No. 2002-69116, JP-A No. 2003-105015, and the like.
Here, as the particulate carrier used for the component (y-1) and the component (y-2), inorganic oxides such as silica, alumina, magnesia, silica alumina, silica magnesia, magnesium chloride, magnesium oxychloride, chloride Examples thereof include inorganic halides such as aluminum and lanthanum chloride, and porous organic carriers such as polypropylene, polyethylene, polystyrene, styrene divinyl benzene copolymer, and acrylic acid copolymer.

Further, as a non-limiting specific example of the component (y), as the component (y-1), a fine particle carrier on which methylalumoxane, isobutylalumoxane, methylisobutylalumoxane, aluminum butylboronate tetraisobutyl, etc. are supported As component (y-2), triphenylborane, tris (3,5-difluorophenyl) borane, tris (pentafluorophenyl) borane, triphenylcarbonium tetrakis (pentafluorophenyl) borate, N, N-dimethyl A particulate carrier carrying anilinium tetrakis (pentafluorophenyl) borate, etc., component (y-3), alumina, silica alumina, magnesium chloride, etc., component (y-4), montmorillonite, zakonite, beidellite , Nontronic , Saponite, hectorite, stevensite, bentonite, smectite group such as taeniolite, vermiculite, and the like mica group. These may form a mixed layer.
Particularly preferred among the above components (y) is the ion-exchange layered silicate of component (y-4), and more preferred are chemical treatments such as acid treatment, alkali treatment, salt treatment, and organic matter treatment. It is an ion exchange layered silicate applied.

Ingredient (z)
Examples of the organoaluminum compound used as the component (z) as necessary include the following general formula AlR _a X _3-a
(Wherein R is a hydrocarbon group having 1 to 20 carbon atoms, X is hydrogen, halogen, alkoxy group, a is a number of 0 <a ≦ 3)
Or a trialkylaluminum such as trimethylaluminum, triethylaluminum, tripropylaluminum or triisobutylaluminum, or a halogen or alkoxy-containing alkylaluminum such as diethylaluminum monochloride or diethylaluminum monomethoxide. In addition, aluminoxanes such as methylaluminoxane can also be used. Of these, trialkylaluminum is particularly preferred.

The catalyst is formed by bringing the component (x), the component (y) and, if necessary, the component (z) into contact with each other. The contact method is not particularly limited, but the contact can be made in the following order. Moreover, this contact may be performed not only at the time of catalyst preparation but also at the time of prepolymerization with olefin or at the time of polymerization of olefin.
(I) Component (x) is contacted with component (y) (ii) Component (x) is contacted with component (y), and then component (z) is added (iii) Component (x) and component (z) ) Is added and then component (y) is added. (Iv) Component (y) and component (z) are contacted and then component (x) is added. (V) The three components are contacted simultaneously.

The amount of components (x), (y) and (z) used in the present invention is arbitrary. For example, the amount of component (x) used relative to component (y) is preferably in the range of 0.1 to 1,000 μmol, particularly preferably 0.5 to 500 μmol, relative to 1 g of component (y). The amount of component (z) used relative to component (y) is preferably such that the amount of transition metal is 0.001 to 100 μmol, particularly preferably 0.005 to 50 μmol, relative to 1 g of component (z). Therefore, the amount of the component (z) to the component (x) is preferably in the range of 10 ⁻⁵ to 50, particularly preferably 10 ^{−4 to} 5 in terms of the molar ratio of the transition metal.

It is preferable that the catalyst of the present invention is subjected to a prepolymerization treatment comprising a small amount of polymerization by contacting olefin in advance. The olefin to be used is not particularly limited, but ethylene, propylene, 1-butene, 1-hexene, 1-octene, 4-methyl-1-pentene, 3-methyl-1-butene, vinylcycloalkane, styrene and the like can be used. It is possible to use, and it is particularly preferable to use propylene. The olefin can be supplied by any method, such as a supply method for maintaining the olefin at a constant speed or in a constant pressure state, a combination thereof, or a stepwise change. The prepolymerization temperature and time are not particularly limited, but are preferably in the range of −20 ° C. to 100 ° C. and 5 minutes to 24 hours, respectively. The amount of prepolymerization is preferably 0.01 to 100, more preferably 0.1 to 50 with respect to the component (y). After completion of the prepolymerization, the catalyst can be used as it is, depending on the usage form of the catalyst, but may be dried if necessary.
Furthermore, a polymer such as polyethylene, polypropylene, or polystyrene, or an inorganic oxide solid such as silica or titania can be allowed to coexist during or after the contact of the above components.

In producing the component propylene-ethylene block copolymer (A) of the present invention, the crystalline propylene-ethylene random copolymer component (A1) and the low crystalline or amorphous propylene-ethylene random copolymer are used. It is necessary to sequentially polymerize the combined component (A2).
When the propylene-ethylene block copolymer is a random copolymer obtained by simply copolymerizing ethylene with propylene, if the ethylene content is low, the flexibility, impact resistance and transparency are not sufficient, and these physical properties are improved. Therefore, when the ethylene content is increased, the heat resistance is extremely deteriorated and the production becomes difficult, and it is difficult to satisfy all the required qualities.
Therefore, in the present invention, the propylene-ethylene block copolymer is a block copolymer obtained by sequentially polymerizing components having different ethylene contents in the first step and the second step. Necessary to balance.
Further, in the present invention, a copolymer having a low molecular weight and easily sticking alone may be used as the component (A2). Therefore, in order to prevent problems such as adhesion to the reactor, the component (A1) is polymerized. It is desirable to use a method of polymerizing component (A2).

(I) Sequential polymerization In producing the component propylene-ethylene block copolymer (A) of the present invention, the crystalline propylene-ethylene random copolymer component (A1) and the low crystalline or amorphous propylene-ethylene are used. It is necessary to sequentially polymerize the random copolymer component (A2) for the reasons described above.
When performing sequential polymerization, either a batch method or a continuous method can be used, but it is generally desirable to use a continuous method from the viewpoint of productivity.
In the case of a batch method, it is possible to polymerize component (A1) and component (A2) separately using a single reactor by changing the polymerization conditions with time. As long as the effects of the present invention are not impaired, a plurality of reactors may be connected in parallel.
In the case of the continuous method, it is necessary to use a production facility in which two or more reactors are connected in series because it is necessary to individually polymerize the component (A1) and the component (A2), but as long as the effect of the present invention is not impaired. A plurality of reactors may be connected in series and / or in parallel for each of component (A1) and component (A2).

(Ii) Polymerization process As the polymerization process (polymerization method), any polymerization method such as a slurry method, a bulk method, and a gas phase method can be used. Although supercritical conditions can be used as intermediate conditions between the bulk method and the gas phase method, they are substantially the same as the gas phase method, and are therefore included in the gas phase method without particular distinction.
Since the low crystalline or amorphous propylene-ethylene random copolymer component (A2) is easily soluble in organic solvents such as hydrocarbons and liquefied propylene, it is desirable to use a gas phase method for the production of the component (A2).
There is no particular problem in using any process for the production of the crystalline propylene-ethylene random copolymer component (A1). In order to avoid this problem, it is desirable to use a gas phase method.
Therefore, using a continuous method, the crystalline propylene-ethylene random copolymer component (A1) is first polymerized by the bulk method or the gas phase method, and then the low crystalline or amorphous propylene-ethylene random copolymer elastomer is used. It is most desirable to polymerize component (A2) by a gas phase method.

(Iii) Other polymerization conditions The polymerization temperature can be used without any particular problem as long as it is within a commonly used temperature range. Specifically, a range of 0 ° C. to 200 ° C., more preferably 40 ° C. to 100 ° C. can be used. The polymerization pressure varies depending on the process to be selected, but can be used without any problem as long as it is in a pressure range usually used. Specifically, a range of greater than 0 to 200 MPa, more preferably 0.1 MPa to 50 MPa can be used. At this time, an inert gas such as nitrogen can be coexisted.
In the case where the sequential polymerization of the component (A1) in the first step and the component (A2) in the second step is performed, it is desirable to add a polymerization inhibitor into the system in the second step. In the case of producing a propylene-ethylene block copolymer, if a polymerization inhibitor is added to a reactor that performs ethylene-propylene random copolymerization in the second step, the particle properties (fluidity, etc.) of the resulting powder, gel, etc. Product quality can be improved. Various technical studies have been made on this technique, and examples thereof include Japanese Patent Publication Nos. 63-54296, 7-25960, and 2003-2939. It is desirable to apply the method to the present invention.

  In addition, each element of the propylene-ethylene block copolymer (A) used for the polypropylene film of the present invention is controlled as follows, and is required for the propylene-ethylene block copolymer (A) of the present invention. Can be manufactured to meet the structural requirements.

(A) Component (A1) For the crystalline propylene-ethylene random copolymer component (A1), it is necessary to control the ethylene content ([E] _A1 ) and T (A1).
In the present invention, in order to control [E] _A1 within a predetermined range, the amount ratio of propylene and ethylene supplied to the polymerization tank in the first step may be appropriately adjusted. The relationship between the supply ratio and the ethylene content in the resulting propylene-ethylene random copolymer varies depending on the type of metallocene catalyst used, but the component (A1) having an ethylene content [E] _A1 required by adjusting the supply ratio Can be manufactured. For example, when [E] _A1 is controlled to 0 to 7 wt%, the supply weight ratio of ethylene to propylene may be in the range of 0 to 0.3, preferably in the range of 0 to 0.2.
At this time, the component (A1) has a narrow crystallinity distribution, and T (A1) decreases with an increase in [E] _A1 . Therefore, in order for T (A1) to satisfy the scope of the present invention, [E] _A1 and the relationship between these are grasped and adjusted to take the target range.

(B) Component (A2) For the low crystalline or amorphous propylene-ethylene random copolymer component (A2), it is necessary to control the ethylene content [E] _A2 , T (A2) and [η] cxs. is there.
In the present invention, in order to control [E] _A2 within a predetermined range, the ratio of ethylene supply to propylene in the second step may be controlled in the same manner as [E] _A1 . For example, when [E] _A2 is controlled to 5 to 20 wt%, the supply weight ratio of ethylene to propylene may be in the range of 0.01 to 5, preferably in the range of 0.05 to 2. At this time, although the crystallinity distribution of the component (A2) is slightly increased with the increase of the ethylene content, T (A2) is decreased with the increase of [E] _A2 as in the case of the component (A1).
Therefore, in order for T (A2) to satisfy the scope of the present invention, the relationship between [E] _A2 and T (A2) is grasped, and [E] _A2 is controlled to be within a predetermined range. Good. [Η] cxs will be described later.

(C) About W (A1) and W (A2) The amount W (A1) of component (A1) and the amount W (A2) of component (A2) are the production amounts of the first step for producing component (A1). It can be controlled by changing the ratio of the production amount of the component (A2). For example, in order to increase W (A1) and decrease W (A2), the production amount of the second step may be reduced while maintaining the production amount of the first step, which shortens the residence time of the second step. It can be easily controlled by lowering the polymerization temperature or increasing the amount of the polymerization inhibitor. The reverse is also true.
When actually setting the conditions, it is necessary to consider the activity decay. That is, in the range of the ethylene contents [E] _A1 and [E] _A2 to be carried out in the present invention, generally, when the ratio of ethylene supply to propylene is increased in order to increase the ethylene content, the polymerization activity is increased. The activity decay tends to increase. Therefore, in order to maintain the activity of the second step, it is necessary to suppress the polymerization activity of the first step. Specifically, the production amount W (A1) is lowered in the first step, and the polymerization is performed as necessary. Lower the temperature and / or shorten the polymerization time (residence time), or increase the ethylene content [E] _A2 in the second step, increase the production W (A2), and raise the polymerization temperature as necessary And / or conditions may be set in such a way as to increase the polymerization time (residence time).

(D) Glass transition temperature Tg In the propylene-ethylene block copolymer (A) used in the present invention, the glass transition temperature Tg needs to have a single peak. In order for Tg to have a single peak, the difference [E] gap between the ethylene content [E] _A1 in component (A1) and the ethylene content [E] _A2 in component (A2), ie [E _A2− [E] _{A1 is set} to 20 wt% or less, preferably 18 wt% or less, more preferably 15 wt% or less, and [E] gap may be reduced to a range where Tg becomes a single peak in actual measurement.
Depending on the ethylene content [E] _A1 of the crystalline copolymer component (A1), the ethylene content [E] _A2 of the low crystalline or amorphous copolymer component (A2) should be within the proper range. By setting the supply weight ratio of ethylene to propylene during the polymerization of component (A2), it is possible to obtain a polymer having a predetermined [E] gap.
The Tg of the block copolymer which does not take a phase separation structure as in the present invention is the ethylene content [E] _A1 in the component (A1) and the ethylene content [E] _A2 in the component (A2), and It is affected by the ratio of both components. In the present invention, the amount of the component (A2) is 5 to 70 wt%, but in this range, Tg is more strongly affected by the ethylene content [E] _{A2 in} the component (A2). That is, Tg reflects the glass transition of the amorphous part, whereas in the block copolymer component (A) of the present invention, the component (A1) has crystallinity and relatively few amorphous parts, This is because component (A2) is low crystalline or amorphous and most of it is an amorphous part.
Therefore, the value of Tg is controlled by substantially _{[E] A2,} the control method of _{[E] A2} are as described above.

(E) Melt flow rate (MFR) In the propylene-ethylene block copolymer (A) of the present invention, in order to maintain transparency, the crystalline copolymer component (A1) and low crystallinity or non-crystallinity. Since it is essential that the copolymer elastomer component (A2) is compatible, the viscosity [η] A1 of the component (A1), the viscosity [η] A2 of the component (A2), propylene-ethylene block copolymer An apparent viscosity mixing rule is generally established between the total viscosity [η] W of the combined (A). That is,
Log [η] W = {W (A1) × Log [η] A1 + W (A2) × Log [η] A2} / 100
Is generally established. In general, there is a certain correlation between MFR and [η], so from the viewpoint of flexibility and heat resistance, [η] A2, W (A1), and W (A2) are set first. The MFR can be freely controlled by changing [η] A1 according to the above equation.

(F) About T (A4) T (A) is an index indicating the crystallinity distribution. Since T (A4) is closer to T (A1) (lower) as the crystallinity distribution of component (A1) is narrower, controlling (A4) to be lower is the crystal of component (A1) and component (A2). It is none other than controlling the sex distribution narrowly.
In general, by using a metallocene catalyst, a polymer having a narrower crystallinity distribution can be obtained than when using a Ziegler-Natta catalyst. In order to narrow the property distribution, it is not necessary and sufficient to use a metallocene catalyst.

  In order to adjust the final propylene-ethylene block copolymer (A) to those having desirable physical properties, the component (A1) and the component (A2) need to have different specific polymer compositions. That is, in the first step and the second step, it is necessary to keep the polymerization conditions corresponding to the respective polymer compositions, particularly the monomer gas composition, at different specific values. Therefore, when the crystallinity distribution of the component (A2) is wide in the adopted process, the transfer step is adjusted so that the specific monomer gas mixture corresponding to the first step is not brought into the second step from the first step. It is necessary to devise such as. Specifically, the crystallinity distribution of the component (A2) can be narrowed by increasing the purge amount in the transfer step, or by diluting or substituting with an inert gas such as nitrogen.

(G) About W (Mw ≦ 5,000) Generally, a polymer having a narrower molecular weight distribution than that of a Ziegler-Natta catalyst can be obtained by using a metallocene catalyst. However, in a system that performs sequential polymerization as in the present invention, it is not always sufficient to use a metallocene catalyst in order to narrow the molecular weight distribution. In particular, in order to prevent the formation of low molecular weight components, the time for transferring from the first step to the second step can be shortened, or the monomer gas mixture corresponding to the first step in the transfer step can be replaced with an inert gas such as nitrogen. By completely substituting, W (Mw ≦ 5,000) can be controlled to be small independently of the polymerization conditions.

(H) Intrinsic Viscosity For [η] cxs, since the propylene-ethylene block copolymer (A) of the present invention uses a metallocene catalyst, the component (A1) contains almost no CXS component. It can be controlled by changing the molecular weight of the component (A2). In order to control [η] cxs, the ratio of hydrogen supply to the monomer in the second step may be controlled as usual. In general, a metallocene catalyst tends to have a lower molecular weight of the polymer as the polymerization temperature is higher. Therefore, it is possible to control [η] cxs by changing the polymerization temperature. [Η] cxs can also be controlled by combining both the hydrogen supply ratio and the polymerization temperature.

2. Adhesive layer In the surface protective film of the present invention, an adhesive layer is formed on one surface of the base material layer made of the propylene-ethylene block copolymer (A), and the adhesive is an acrylic adhesive (B). Is used.
By using an acrylic pressure-sensitive adhesive for the pressure-sensitive adhesive layer, when at least one of the base material layer and the pressure-sensitive adhesive layer is laminated in a molten state, the adhesive layer is firmly bonded, and therefore, the delamination property is excellent. Since the adhesive layer and the base material layer are firmly bonded, for example, after the surface protective film of the present invention is attached to the adherend, the adhesive layer does not remain on the adherend even if it is peeled off again. It can also be used as a surface protective film that can be repeatedly applied.
The acrylic pressure-sensitive adhesive is not particularly limited as long as the effects of the present invention are not impaired, but an acrylic pressure-sensitive adhesive containing a (meth) acrylic polymer containing a hydroxyl group as a functional group and an isocyanate-based crosslinking agent, etc. can give. An acrylic pressure-sensitive adhesive containing a (meth) acrylic polymer containing a hydroxyl group as a functional group and an isocyanate-based crosslinking agent is used from the balance of transparency, cohesiveness, and peeling properties.

  The (meth) acrylic polymer in the present invention contains an alkyl (meth) acrylate and a hydroxyl group-containing monomer as monomer units. The technique for introducing a hydroxyl group is not particularly limited, but for example, a technique for copolymerizing a hydroxyl group-containing monomer can be easily performed.

  In addition, the (meth) acrylic polymer in the present invention refers to an acrylic polymer and / or a methacrylic polymer, (meth) acrylate refers to an acrylate and / or methacrylate, and an alkyl (meth) acrylate includes Refers to alkyl acrylate and / or alkyl methacrylate.

  Examples of the alkyl (meth) acrylate include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, and the like. Can be given. These compounds may be used alone or in combination of two or more.

  Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, 8-hydroxyoctyl ( (Meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate, (4-hydroxymethylcyclohexyl) methyl acrylate, N-methylol (meth) acrylamide, N-hydroxy (meth) acrylamide, Examples include vinyl alcohol, allyl alcohol, 2-hydroxyethyl vinyl ether, 4-hydroxybutyl vinyl ether, and diethylene glycol monovinyl ether. These monomers may be used alone or in combination of two or more.

  The hydroxyl group-containing monomer may be used alone or in combination of two or more, but the total content is 1 to 100 parts by weight of the (meth) acrylic polymer. The amount is preferably 10 parts by weight, and more preferably 2 to 6 parts by weight. By copolymerizing the hydroxyl group-containing monomer, a reactive site due to crosslinking or the like is given.

  The (meth) acrylic polymer used in the present invention preferably has a weight average molecular weight of about 300,000 to 2.5 million. When the weight average molecular weight is smaller than 300,000, the adhesive force tends to be generated due to the reduced cohesive force of the pressure-sensitive adhesive composition. A weight average molecular weight means what was obtained by measuring by GPC (gel permeation chromatography).

In addition, the glass transition temperature (Tg) of the (meth) acrylic polymer is preferably 0 ° C. or lower (usually −100 ° C. or higher), preferably −10 ° C. or lower for the reason that it is easy to balance the adhesive performance. When the glass transition temperature is higher than 0 ° C., the polymer is difficult to flow and the wetting to the polarizing plate is insufficient, and there is a tendency to cause blisters generated between the polarizing plate and the pressure-sensitive adhesive composition layer of the pressure-sensitive adhesive sheet. is there.
In addition, the glass transition temperature (Tg) of a (meth) acrylic-type polymer can be adjusted in the said range by changing the monomer component and composition ratio to be used suitably.

  Moreover, as other polymerizable monomers other than the above-mentioned monomers, it is possible to use a polymerizable monomer for adjusting the glass transition point and peelability of the (meth) acrylic polymer as long as the effects of the present invention are not impaired. it can.

  Other polymerizable monomers used in (meth) acrylic polymers include, for example, cohesion and heat resistance of sulfonic acid group-containing monomers, phosphate group-containing monomers, cyano group-containing monomers, vinyl ester monomers, aromatic vinyl monomers, etc. It has a functional group that acts as a crosslinking point and improves adhesion, such as an acid-improving component, an acid anhydride group-containing monomer, an amide group-containing monomer, an amino group-containing monomer, an epoxy group-containing monomer, N-acryloylmorpholine, and a vinyl ether monomer. Components can be used as appropriate. These monomer compounds may be used alone or in admixture of two or more.

  Examples of the sulfonic acid group-containing monomer include styrene sulfonic acid, allyl sulfonic acid, 2- (meth) acrylamide-2-methylpropane sulfonic acid, (meth) acrylamide propane sulfonic acid, sulfopropyl (meth) acrylate, (meth And acryloyloxynaphthalene sulfonic acid.

  Examples of the phosphoric acid group-containing monomer include 2-hydroxyethylacryloyl phosphate.

  Examples of the cyano group-containing monomer include acrylonitrile and methacrylonitrile.

  Examples of the vinyl ester monomer include vinyl acetate, vinyl propionate, vinyl laurate, and the like.

  Examples of the aromatic vinyl monomer include styrene, chlorostyrene, chloromethyl styrene, α-methyl styrene, and the like.

  Examples of the acid anhydride group-containing monomer include maleic anhydride and itaconic anhydride.

  Examples of the amide group-containing monomer include acrylamide and diethyl acrylamide.

  Examples of the amino group-containing monomer include N, N-dimethylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylate, N- (meth) acryloylmorpholine, and alkylaminoalkyl (meth) acrylate. Examples include esters.

  Examples of the epoxy group-containing monomer include glycidyl (meth) acrylate and allyl glycidyl ether.

  Examples of the vinyl ether monomer include methyl vinyl ether, ethyl vinyl ether, isobutyl vinyl ether, and the like.

  In the present invention, other polymerizable monomers may be used alone or in combination of two or more, but the total content is 100 parts by weight of the (meth) acrylic polymer. On the other hand, it is preferably 0 to 300 parts by weight, and more preferably 0 to 150 parts by weight.

  In addition, the polymerization method in particular of (meth) acrylic-type polymer is not restrict | limited, Well-known polymerization methods, such as solution polymerization, emulsion polymerization, suspension polymerization, and UV polymerization, are employable. Further, the obtained copolymer may be any of a random copolymer, a block copolymer, a graft copolymer, and the like.

  The pressure-sensitive adhesive composition of the present invention is based on the (meth) acrylic polymer as described above.

  In the present invention, an isocyanate crosslinking agent and / or an epoxy crosslinking agent is used as the crosslinking agent. Isocyanate-based crosslinking agents and epoxy-based crosslinking agents are used for imparting adhesion and cohesiveness with the base material layer.

  As the isocyanate-based crosslinking agent, a polyfunctional isocyanate compound is used, and various compounds having two or more isocyanate groups in the molecule are included.

  Examples of the isocyanate compound include lower aliphatic polyisocyanates such as butylene diisocyanate and hexamethylene diisocyanate, alicyclic isocyanates such as cyclopentylene diisocyanate, cyclohexylene diisocyanate, and isophorone diisocyanate, 2,4-tolylene diisocyanate, Aromatic isocyanates such as 4,4′-diphenylmethane diisocyanate and xylylene diisocyanate, trimethylolpropane / tolylene diisocyanate trimer adduct (trade name Coronate L, manufactured by Nippon Polyurethane Industry Co., Ltd.), trimethylolpropane / hexamethylene Diisocyanate trimer adduct (trade name Coronate HL, manufactured by Nippon Polyurethane Industry Co., Ltd.), isocyanurate of hexamethylene diisocyanate Body (trade name: Coronate HX, manufactured by Nippon Polyurethane Industry Co., Ltd.) and isocyanate adducts and the like. Among these, those having an isocyanurate ring are particularly preferred. For example, polyisocyanate having a long-chain alkylene diol-modified isocyanurate ring (manufactured by Dainippon Ink & Chemicals, Vernock DN-995), isocyanurate of hexamethylene diisocyanate. (Trade name Coronate HX, manufactured by Nippon Polyurethane Industry Co., Ltd.). These compounds may be used alone or in combination.

  The content of the crosslinking agent used in the present invention may be blended to such an extent that it does not affect the physical properties of the adhesive, but is usually contained in an amount of 0.2 to 10 parts by weight with respect to 100 parts by weight of the (meth) acrylic polymer, It is preferable that 0.5-8 weight part is contained, and it is more preferable that 1-6 weight part is contained.

  As an epoxy type crosslinking agent, a polyfunctional epoxy compound is used, and various compounds having two or more epoxy groups in the molecule are included. Typical examples include sorbitol tetraglycidyl ether, trimethylolpropane glycidyl ether, tetraglycidyl-1,3-bisaminomethylcyclohexane, tetraglycidyl-m-xylenediamine, and triglycidyl-p-aminophenol. It is done. Examples of commercially available epoxy crosslinking agents include Tetrad C (manufactured by Mitsubishi Gas Chemical Co., Inc.).

  The number of parts of the epoxy crosslinking agent is generally 1 to 8 parts by weight per 100 parts by weight of the acrylic polymer, although it depends on the amount of acid introduced into the acrylic polymer and the structure of the epoxy crosslinking agent. It is preferable to contain 1-6 weight part.

  For the acrylic pressure-sensitive adhesive, a crosslinking agent (polyamine compound, melamine resin, aziridine derivative, urea resin) other than those exemplified above can also be used as appropriate. These components may be used alone or in combination of two or more.

  Examples of commercially available acrylic pressure-sensitive adhesives include trade name: AG105 manufactured by Soken Chemical Co., Ltd.

  In addition, when the adhesive layer is laminated by coextrusion molding with an extruder, an adhesive is added to the propylene-ethylene block copolymer used for the base material layer of the present invention in consideration of adhesion to the base material layer. It can mix | blend and can be used as an adhesive layer. When the propylene-ethylene block copolymer used in the present invention is blended with the above-mentioned pressure-sensitive adhesive, the total amount of propylene-ethylene block copolymer and pressure-sensitive adhesive used in the present invention is 100% by weight. -Content of an ethylene block copolymer is 1 to 99 weight%, and content of an adhesive is 99 to 1 weight%. Preferably, the content of the propylene-ethylene block copolymer is 5 to 75% by weight, the content of the pressure-sensitive adhesive is 95 to 25% by weight, and more preferably, the content of the propylene-ethylene block copolymer is 10 to 10%. The content of the pressure-sensitive adhesive is 50 to 90% by weight.

3. Release treatment layer
In the surface protective film of the present invention, a release treatment layer is formed on the other surface of the pressure-sensitive adhesive layer formed on one of the base material layers made of the propylene-ethylene block copolymer. By using a layer formed of a silicone-based or long-chain alkyl-based release treatment agent (C) as the release treatment layer, the roll is unwound from the roll winding state where both the adhesive layer and the release treatment layer are in contact with each other in a solid state. Sometimes the film can be peeled off smoothly, and when used, it can be made into a film for surface protection having the property that the feeding property is improved. Moreover, since it is possible to improve the feedability without roughening the surface of the release treatment layer, it is possible to obtain a surface protective film while maintaining excellent transparency.

  As the silicone-based release treatment agent used in the layer formed of the silicone-based or long-chain alkyl release treatment agent, a commonly used silicone-based release treatment agent mainly composed of dimethylpolysiloxane can also be used. It is also possible to use a silicone release treatment agent containing a three-dimensional organopolysiloxane. Specifically, a silicone-based mold release agent containing organopolysiloxane as a main component and blending cellulose derivatives such as methyl cellulose, ethyl cellulose and acetyl cellulose, alkyd resins, and the like is preferably used. By incorporating a cellulose derivative, an alkyd resin, or the like, it is possible to control the release property of the silicone release agent. Cellulose derivatives and alkyd resins are preferably blended in an amount of 5 to 50% by weight in the silicone release agent.

Depending on the type of curing reaction (crosslinking reaction) of the organopolysiloxane, it is roughly divided into a condensation reaction type and an addition reaction type, but in the present invention, any reaction type may be used.
For example, as the condensation reaction type silicone release agent, for example, a silicone release agent in which a cellulose derivative or an alkyd resin is blended with an organopolysiloxane having a silanol group at a molecular terminal is mentioned. Here, as the organopolysiloxane having a silanol group at the molecular end, a polysiloxane in which an alkyl group such as a methyl group or an ethyl group or a phenyl group is introduced as a side chain functional group (for example, dimethyl diphenylpolysiloxane) is used. It is preferable that the release agent has a good compatibility with the cellulose derivative and the alkyd resin, and a stable release property. In addition, the organopolysiloxane having a silanol group at the molecular end is appropriately blended with a crosslinking agent such as an alkoxy group-containing organopolysiloxane, or a catalyst such as dibutyltin dilaurate, dibutyltin diacetate, dibutyltin dioctate, or zinc octylate. May be. Moreover, resin, such as an acrylic resin, can also be suitably mix | blended as a 3rd component as needed. In the silicone release agent, the crosslinking agent is preferably 4 to 20% by weight, the catalyst is preferably 5 to 10% by weight, and the resin as the third component is preferably 5 to 26% by weight.

  As an addition reaction type silicone release agent, for example, a silicone release agent in which a cellulose derivative or alkyd resin is blended with organopolysiloxane having at least two alkenyl groups such as vinyl groups bonded to silicon atoms in one molecule. Agents. Here, as the above-mentioned organopolysiloxane, it is preferable to use an organopolysiloxane having an alkyl group such as a methyl group or an ethyl group or a phenyl group introduced as a functional group of the side chain, whereby cellulose derivatives or alkyds are used. A release agent having good compatibility with the resin and stable release characteristics can be obtained. The organopolysiloxane may be appropriately blended with a crosslinking agent such as an organohydrodiene polysiloxane and a catalyst such as a platinum compound such as chloroplatinic acid.

  The above-mentioned silicone release agent can be appropriately selected from commercially available products. For example, as a condensation reaction type silicone release agent, KS available from Shin-Etsu Chemical Co., Ltd. -723A / B (consisting of dimethyl diphenylpolysiloxane, methoxysilicone and ethylcellulose) is X-62-9201A / B available from Shin-Etsu Chemical Co., Ltd. as an addition reaction type silicone release agent. be able to.

Moreover, as a long-chain alkyl release agent used in a layer formed of a silicone-based or long-chain alkyl release agent, a polymer of a long-chain alkyl acrylate having 12 or more carbon atoms, a long-chain alkyl acrylate, and the like And a release treatment agent obtained from a reaction product obtained by reacting a long-chain alkyl component such as a long-chain alkyl isocyanate with a copolymer of the above-mentioned vinyl monomer or polyvinyl alcohol.
For example, BP type manufactured by Nitto Denko Corporation, ashioresin manufactured by Ashio Sangyo Co., Ltd., and Pyroleil manufactured by Yushi Co., Ltd. can be used.
In addition, the release treatment layer includes a method of forming a release treatment layer by applying a silicone-based or long-chain alkyl release treatment agent, but considering the adhesion with the base material layer, the base material layer of the present invention The propylene-ethylene block copolymer (A) can be blended with a release treatment agent and used as a release treatment layer. When the release agent is blended and used in the propylene-ethylene block copolymer (A) for the substrate layer of the present invention, the propylene-ethylene block copolymer (A) for the substrate layer of the present invention and the release treatment are used. When the total amount of the agent is 100% by weight, the content of the propylene-ethylene block copolymer (A) for the base material layer of the present invention is 99 to 99.95% by weight, and the content of the release treatment agent is 1 ~ 0.05% by weight.

4). Resin compounding agent that can be used in each layer The substrate layer made of the propylene-ethylene block copolymer in the present invention, the pressure-sensitive adhesive layer, and the release treatment layer that is used as needed include film-forming stability and secondary processing. Various additives used as known resin compounding agents, for example, antioxidants, anti-blocking agents, slip agents, as long as the purpose of the present invention is not impaired from the maintenance of quality as a film for surface handling and surface protection , Nucleating agent, neutralizing agent, light stabilizer, antistatic agent, tackifier and the like may be contained. Various additives are described in detail below.

(1) Antioxidants As antioxidants, specific examples of phenolic antioxidants include tris- (3,5-di-t-butyl-4-hydroxybenzyl) -isocyanurate, 1,1,3- Tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, octadecyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, pentaerythrityl-tetrakis {3- ( 3,5-di-tert-butyl-4-hydroxyphenyl) propionate}, 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl) benzene 3,9-bis [2- {3- (3-t-butyl-4-hydroxy-5-methylphenyl) propionyloxy} -1,1-dimethylethyl] -2,4,8,10- Examples thereof include tetraoxaspiro [5,5] undecane, 1,3,5-tris (4-t-butyl-3-hydroxy-2,6-dimethylbenzyl) isocyanuric acid and the like.

Specific examples of phosphorus antioxidants include tris (mixed, mono and dinonylphenyl phosphite), tris (2,4-di-t-butylphenyl) phosphite, 4,4′-butylidenebis (3- Methyl-6-tert-butylphenyl-di-tridecyl) phosphite, 1,1,3-tris (2-methyl-4-di-tridecylphosphite-5-tert-butylphenyl) butane, bis (2, 4-di-t-butylphenyl) pentaerythritol-di-phosphite, tetrakis (2,4-di-t-butylphenyl) -4,4'-biphenylenediphosphonite, tetrakis (2,4-di-t -Butyl-5-methylphenyl) -4,4'-biphenylenediphosphonite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol-di-phos You can list s fights.
Specific examples of the sulfur-based antioxidant include di-stearyl-thio-di-propionate, di-myristyl-thio-di-propionate, pentaerythritol-tetrakis- (3-lauryl-thio-propionate), and the like. it can.
These antioxidants can be used singly or in combination of two or more as long as the effects of the present object are not impaired.

  The compounding quantity of antioxidant is 0.01-1.0 weight part with respect to 100 weight part of each resin used for each layer of a base material layer, an adhesion layer, and a peeling process layer, Preferably it is 0.02-0. 5 parts by weight, more preferably 0.05 to 0.1 parts by weight. When the blending amount of the antioxidant is within the above range, the thermal stability is improved and the deterioration of the resin causing fish eyes is suppressed.

(2) Antiblocking agent The antiblocking agent has an average particle diameter of 1 to 7 μm, preferably 1 to 5 μm, and more preferably 1 to 4 μm. If the average particle diameter is less than 1 μm, the slipperiness and openability of the resulting film are inferior. On the other hand, if it exceeds 7 μm, the transparency and scratching property are remarkably inferior. Here, the average particle diameter is a value obtained by Coulter counter measurement.

Specific examples of the anti-blocking agent include, for example, inorganic or synthetic silica (silicon dioxide), magnesium silicate, aluminosilicate, talc, zeolite, aluminum borate, calcium carbonate, calcium sulfate, barium sulfate, calcium phosphate. Etc. are used.
Moreover, as an organic type, polymethyl methacrylate, polymethylsilyltosesquioxane (silicone), polyamide, polytetrafluoroethylene, epoxy resin, polyester resin, benzoguanamine / formaldehyde (urea resin), phenol resin, etc. may be used. it can.
In particular, synthetic silica and polymethyl methacrylate are preferable from the balance of dispersibility, transparency, blocking resistance, and scratch resistance.
The anti-blocking agent may be surface-treated, and as the surface treating agent, surfactant, metal soap, acrylic acid, oxalic acid, citric acid, tartaric acid and other organic acids, higher alcohols, esters, Condensed phosphates such as silicone, fluorine resin, silane coupling agent, sodium hexametaphosphate, sodium pyrophosphate, sodium tripolyphosphate, sodium trimetaphosphate, etc. can be used, especially those with citric acid treatment among organic acid treatments Is preferred. The treatment method is not particularly limited, and a known method such as surface spraying or dipping can be employed.
The anti-blocking agent may have any shape, and can be any shape such as a spherical shape, a square shape, a columnar shape, a needle shape, a plate shape, and an indefinite shape.
These anti-blocking agents can be used singly or in combination of two or more in a range that does not impair the effects of this object.

  When the antiblocking agent is blended, the blending amount is 0.01 to 1.0 part by weight with respect to 100 parts by weight of each resin used in each of the base layer, the adhesive layer and the release treatment layer, preferably 0.00. It is 05-0.7 weight part, More preferably, it is 0.1-0.5 weight part. When the blending amount of the anti-blocking agent is within the above range, the blocking property is improved and the feeding property is improved.

(3) Slip agent Examples of the slip agent include monoamides, substituted amides, bisamides, and the like, which can be used alone or in combination of two or more.
Specific examples of monoamides include lauric acid amide, palmitic acid amide, stearic acid amide, behenic acid amide, hydroxystearic acid amide and the like as saturated fatty acid monoamides.
Examples of the unsaturated fatty acid monoamide include oleic acid amide, erucic acid amide, ricinoleic acid amide and the like.
Specific examples of substituted amides include N-stearyl stearic acid amide, N-oleyl oleic acid amide, N-stearyl oleic acid amide, N-oleyl stearic acid amide, N-stearyl erucic acid amide, N-oleyl palmitic acid amide Etc.
Specific examples of bisamides include, as saturated fatty acid bisamides, methylene bis stearic acid amide, ethylene biscapric acid amide, ethylene bis lauric acid amide, ethylene bis stearic acid amide, ethylene bisisostearic acid amide, ethylene bishydroxystearic acid amide, Ethylene bisbehenic acid amide, hexamethylene bis stearic acid amide, hexamethylene bis behenic acid amide, hexamethylene bishydroxy stearic acid amide, N, N'-distearyl adipic acid amide, N, N'-distearyl Sepacic acid amide and the like can be mentioned.
Examples of the unsaturated fatty acid bisamide include ethylene bisoleic acid amide, hexamethylene bisoleic acid amide, N, N′-dioleyl adipic acid amide, N, N′-dioleyl sepasin acid amide and the like.
Examples of the aromatic bisamide include m-xylylene bis stearic acid amide and N, N′-distearylisophthalic acid amide.
Among these, oleic acid amide, erucic acid amide, and behenic acid amide are particularly preferably used among the fatty acid amides.

  The amount of the slip agent to be blended is 0.01 to 1.0 part by weight, preferably 0 with respect to 100 parts by weight of each resin used for each of the base layer, the adhesive layer and the release treatment layer. 0.05 to 0.7 parts by weight, more preferably 0.1 to 0.4 parts by weight. When the blending amount of the slip agent is within the above range, the slipping property is improved and the feeding property is improved.

(4) Nucleating agent Specific examples of the nucleating agent include sodium 2,2-methylene-bis (4,6-di-t-butylphenyl) phosphate, talc, 1,3,2,4-di (p-methyl). Benzyl compounds such as benzylidene) sorbitol, hydroxy-di (t-butylaluminum benzoate), 2,2-methylene-bis (4,6-di-t-butylphenyl) phosphoric acid and an aliphatic monocarbon having 8 to 20 carbon atoms Examples thereof include a carboxylic acid lithium salt mixture (manufactured by ADEKA, trade name NA21).
The blending amount when blending the nucleating agent is 0.0005 to 0.5 parts by weight, preferably 100 parts by weight of each resin used in each layer of the base material layer, the adhesive layer and the release treatment layer. 0.001 to 0.1 parts by weight, more preferably 0.005 to 0.05 parts by weight. When the blending amount of the nucleating agent is within the above range, the crystallization speed is increased and the transparency is improved.

Moreover, a high density polyethylene resin can be mentioned as a nucleating agent other than the above. The density of the high-density polyethylene resin is 0.94 to 0.98 g / cm ³ , preferably 0.95 to 0.97 g / 10 cm ³ . If the density is out of this range, the effect of improving transparency cannot be obtained. 190 degreeC melt flow rate (MFR) of a high density polyethylene resin is 5 g / 10min or more, Preferably it is 7-500 g / 10min, More preferably, it is 10-100 g / 10min. When the MFR is less than 5 g / 10 min, the dispersion diameter of the high-density polyethylene resin is not sufficiently small, and it itself becomes a foreign matter and causes fish eyes. In order to finely disperse the high-density polyethylene resin, the MFR of the high-density polyethylene resin is preferably larger than the MFR of the propylene-ethylene block copolymer of the present invention.

  The production of the high-density polyethylene resin used as the nucleating agent is not particularly limited with respect to the polymerization method and catalyst as long as a polymer having the desired physical properties can be produced. For catalysts, Ziegler type catalysts (ie, based on a combination of supported or unsupported halogen-containing titanium compounds and organoaluminum compounds), Kaminsky type catalysts (ie, supported or unsupported metallocene compounds and organoaluminum compounds, especially alumoxanes). Based on the combination). There is no restriction | limiting about the shape of a high density polyethylene-type resin, A pellet form may be sufficient and a powder form may be sufficient.

  When used as a nucleating agent, the blending amount of the high-density polyethylene is 0.01 to 5 parts by weight, preferably 100 parts by weight of each resin used in each layer of the base material layer, the adhesive layer and the release treatment layer. 0.05 to 3 parts by weight, more preferably 0.1 to 1 part by weight. When the blending amount of the high density polyethylene is within the above range, the crystallization speed is increased and the transparency is improved. Further, in the case of coextrusion molding, there is no transfer of the sweeper roll.

(5) Neutralizing agent Specific examples of the neutralizing agent include calcium stearate, zinc stearate, hydrotalcite, Mizukarak (manufactured by Mizusawa Chemical Co., Ltd.), and the like.
The blending amount in the case of blending the neutralizing agent is 0.01 to 1.0 part by weight, preferably 0.00 with respect to 100 parts by weight of each resin used for each of the base layer, the adhesive layer and the release treatment layer. It is 02-0.5 weight part, More preferably, it is 0.05-0.1 weight part. When the blending amount of the neutralizing agent is within the above range, the effect as an internal lubricant is improved, and scraping of deteriorated materials inside the extruder is suppressed.

(6) Light Stabilizer As the light stabilizer, a hindered amine stabilizer is preferably used, and a structure in which all hydrogen bonded to carbons at the 2-position and 6-position of a conventionally known piperidine is substituted with a methyl group. Although the compound which has this is used without being specifically limited, the following compounds are specifically used.
Specific examples include polycondensates of dimethyl oxalate and 1- (2-hydroxyethyl) -4-hydroxy-2,2,6,6-tetramethylpiperidine, tetrakis (1,2,2,6,6). -Pentamethyl-4-piperidyl) 1,2,3,4-butanetetracarboxylate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, N, N-bis (3-aminopropyl) ) Ethylenediamine · 2,4-bis [N-butyl-N- (1,2,2,6,6-pentamethyl-4-piperidyl) amino] -6-chloro-1,3,5-triazine condensate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, poly [{6- (1,1,3,3-tetramethylbutyl) imino-1,3,5-triazine-2,4- Jil} {(2,2, , 6-tetramethyl-4-piperidyl) imino} hexamethylene {2,2,6,6-tetramethyl-4-piperidyl} imino], poly [(6-morpholino-s-triazine-2,4-diyl) And [(2,2,6,6-tetramethyl-4-piperidyl) imino] hexamethylene {(2,2,6,6-tetramethyl-4-piperidyl) imino}].
These hindered amine stabilizers can be used singly or in combination of two or more in a range not impairing the effect of the present object.

When the hindered amine stabilizer is blended, the blending amount is 0.005 to 2 parts by weight, preferably 0.01 to 100 parts by weight of each resin used in each layer of the base material layer, the adhesive layer and the release treatment layer. -1 part by weight, more preferably 0.05-0.5 part by weight.
When the content of the hindered amine stabilizer is within the above range, stability such as heat resistance and aging resistance is improved.

(7) Antistatic agent The antistatic agent can be used without particular limitation as long as it is a known antistatic agent or antistatic agent conventionally used, and examples thereof include anionic surfactants and cations. Ionic surfactants, nonionic surfactants, amphoteric surfactants and the like.

  Examples of the anionic surfactant include fatty acid or rosin acid soap, N-acyl carboxylate, ether carboxylate, carboxylate such as fatty acid amine salt; sulfosuccinate, ester sulfonate, N-acyl sulfonate Sulfonates such as salts; sulfated oils, sulfate esters, alkyl sulfate salts, sulfate sulfate polyoxyethylene salts, sulfate ether salts, sulfate ester salts such as sulfate amide salts; alkyl phosphate salts, alkyl polyoxyethylene phosphates Examples thereof include phosphoric acid ester salts such as salts, phosphoric acid ether salts and phosphoric acid amide salts.

  Examples of the cationic surfactant include amine salts such as alkylamine salts; alkyltrimethylammonium chloride, alkylbenzyldimethylammonium chloride, alkyldihydroxyethylmethylammonium chloride, dialkyldimethylammonium chloride, tetraalkylammonium salt, N, N-di Quaternary ammonium salts such as (polyoxyethylene) dialkylammonium salts and N-alkylalkanamide ammonium salts; 1-hydroxyethyl-2-alkyl-2-imidazoline, 1-hydroxyethyl-1-alkyl-2-alkyl Examples include alkyl imidazoline derivatives such as -2-imidazoline; imidazolinium salts, pyridinium salts, isoquinolinium salts, and the like.

  Examples of the nonionic surfactant include ether forms such as alkyl polyoxyethylene ether and p-alkylphenyl polyoxyethylene ether; fatty acid sorbitan polyoxyethylene ether, fatty acid sorbitol polyoxyethylene ether, fatty acid glycerin polyoxyethylene ether, etc. Ether ester form of fatty acid polyoxyethylene ester, monoglyceride, diglyceride, sorbitan ester, sucrose ester, dihydric alcohol ester, boric acid ester, etc .; dialcohol alkylamine, dialcohol alkylamine ester, fatty acid alkanolamide, N, N-di (polyoxyethylene) alkanamide, alkanolamine ester, N, N-di (polyoxyethylene) alkaneamine, amine oxy De, a nitrogen-formed and fabricated and alkyl polyethylene imine.

  Examples of the amphoteric surfactant include amino acid forms such as monoaminocarboxylic acid and polyaminocarboxylic acid; N-alkyl-β-alanine such as N-alkylaminopropionate and N, N-di (carboxyethyl) alkylamine salt. Forms: Betaine forms such as N-alkylbetaines, N-alkylamidobetaines, N-alkylsulfobetaines, N, N-di (polyoxyethylene) alkylbetaines, imidazolinium betaines; 1-carboxymethyl-1-hydroxy- And alkyl imidazoline derivatives such as 1-hydroxyethyl-2-alkyl-2-imidazoline and 1-sulfoethyl-2-alkyl-2-imidazoline.

  Among these, nonionic surfactants and amphoteric surfactants are preferable. Among them, monoglycerides, diglycerides, boric acid esters, dialcohol alkylamines, dialcohol alkylamine esters, amides and the like or nitrogen-containing non-type surfactants are preferred. Ionic surfactants; betaine amphoteric surfactants are preferred.

  In addition, as an antistatic agent, a commercial item can be used, for example, electro stripper TS5 (trade name, glycerin monostearate manufactured by Kao Corporation), electro stripper TS6 (trade name, stearyl manufactured by Kao Corporation). Diethanolamine), electrostripper EA (trade name, lauryl diethanolamine, manufactured by Kao Corporation), electrostripper EA-7 (trade name, polyoxyethylene laurylamine capryl ester, manufactured by Kao Corporation), Denon 331P (maruhishi oil ( Co., Ltd., trademark, stearyl diethanolamine monostearate), Denon 310 (manufactured by Maruhishi Oil Chemical Co., Ltd., trademark, alkyldiethanolamine fatty acid monoester), Register PE-139 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd., trademark) , Stearic acid mono & diglyceride Ester), Chemistat 4700 (Sanyo Chemical Industries Co., Ltd., trademark, alkyl dimethyl betaine), rheostat S (Lion Co., Ltd., trademark, alkyl diethanolamide), and the like.

  When blending the antistatic agent, the blending amount is 0.01 to 2 parts by weight, preferably 0.05 to 1 with respect to 100 parts by weight of each resin used in the base layer, the adhesive layer and the release treatment layer. Parts by weight, more preferably 0.1 to 0.8 parts by weight, most preferably 0.2 to 0.5 parts by weight. These antistatic agents can be used singly or in combination of two or more in a range that does not impair the effects of this object. When the blending amount of the antistatic agent is within the above range, it is possible to prevent electrification and suppress deposits such as dust.

(8) Tackifier The tackifier includes, for example, aliphatic petroleum resins, alicyclic hydrogenated petroleum resins, aromatic petroleum resins, C5 petroleum resins, terpene resins, coumarone / indene resins, A phenol resin, a rosin resin, a tackifier, etc. are mentioned, These can be used 1 type or in combination of 2 or more types in the range which does not impair the effect of this invention remarkably.

  The blending amount in the case of blending the tackifier is not particularly limited as long as the effects of the present invention are not impaired, but 100 weights of each resin used for each of the base layer, the tacky layer and the release treatment layer. 0.0001 to 200 parts by weight with respect to parts. Preferably it is 0.01-150 weight part, More preferably, it is 1-150 weight part, Most preferably, it is 10-100 weight part. When the compounding amount of the tackifier is within the above range, the adhesive strength is improved.

(9) Others Further, an elastomer is blended as a component for appropriately adjusting flexibility and tackiness within a range that does not significantly impair the effects of the present invention, an ultraviolet absorber, a metal deactivator, a peroxide, and a filler. Antibacterial and antifungal agents, fluorescent whitening agents, antifogging agents, flame retardants, colorants, pigments, natural oils, synthetic oils, waxes, and the like can be blended, and the blending ratio is an appropriate amount.

The above-mentioned various additives can be added directly to each resin used for the base material layer, the adhesive layer, and the release treatment layer and melt kneaded for use, or may be added during melt kneading. Furthermore, it can be added directly after melt-kneading, or can be added as a masterbatch within a range that does not significantly impair the effects of the present invention. Moreover, you may add by these composite methods.
In general, additives such as an antioxidant and a neutralizing agent are blended, mixed, melted and kneaded, and then molded into a product for use. It is also possible to add and use other resins or other additional components (including a masterbatch) as long as the effects of the present invention are not significantly impaired during molding.

  For the above mixing, melting, and kneading, any conventionally known method can be used. Usually, a Henschel mixer, a super mixer, a V blender, a tumbler mixer, a ribbon blender, a Banbury mixer, a kneader blender, a uniaxial or biaxial kneading. It can be carried out in an extruder. Among these, it is preferable to perform mixing or melt-kneading with a uniaxial or biaxial kneading extruder.

5. Production of Surface Protection Film The surface protection film of the present invention can be produced by a known method for producing a laminated film.
For example, it manufactures by well-known techniques, such as a T die-cast method, a water cooling inflation method, an air cooling inflation method.
In the T-die casting method, the resin melt-kneaded by an extruder is extruded from the T-die and cooled by being brought into contact with a roll through which a coolant such as water is passed, and generally has good transparency and good thickness accuracy. A film can be produced. Such a method is a preferable manufacturing method for the film.

  Here, the thickness of the film for surface protection is not particularly limited, but is 10 to 500 μm, preferably 20 to 200 μm, more preferably 30 to 100 μm, and most preferably 40 to 80 μm. If the thickness is outside this range, processing becomes difficult.

As a means of providing the adhesive layer on one side of the base material layer, as a method obtained by application by a solution coating method or the like, an adhesive dissolved in an organic solvent such as a toluene solution is applied to one side of the base material layer by a roll coater or the like Thereafter, a method of forming an adhesive layer by drying can be mentioned. At that time, in order to improve the affinity between the base material layer and the pressure-sensitive adhesive layer, conventionally known corona discharge treatment, plasma discharge treatment, primer treatment, etc. are performed on one surface of the base material layer (adhesion surface with the pressure-sensitive adhesive layer). May be.
In addition, as a method for obtaining the adhesive layer by lamination, the adhesive is heated and melted by an extruder, extruded into a film form from a T die, and laminated on one side of the substrate layer, or the substrate layer is obtained by an extruder. And a method in which the pressure-sensitive adhesive is heated and melted and coextruded into a film shape from a T-die together with the base material layer.
In the present invention, adopting a method in which the adhesive layer is coextruded with the base material layer in the form of a film from a T-die is advantageous in terms of contamination problems and economical points.

  The thickness of the pressure-sensitive adhesive layer is not particularly limited since the pressure-sensitive adhesive strength varies depending on the application. However, in the case of a method of forming a pressure-sensitive adhesive layer by applying a pressure-sensitive adhesive in a subsequent process, it is also melted by heating from an extruder. Also in the case of the method of forming an adhesive layer, it is 0.1-100 micrometers normally, Preferably it is 1-50 micrometers, More preferably, it is 5-30 micrometers, Most preferably, it is 10-20 micrometers.

Examples of means for forming the release treatment layer provided on the other surface of the pressure-sensitive adhesive layer of the surface protective film of the present invention include known methods such as coating, curing, and lamination.
As a method for obtaining the release treatment layer by coating, a release treatment agent dissolved in an organic solvent such as a toluene solution is applied to one side of the base material layer with a roll coater, and then dried to cure the release treatment agent and release. The method of forming a process layer can be mentioned. At that time, in order to improve the affinity between the base material layer and the release treatment layer, conventionally known corona discharge treatment, plasma discharge treatment, primer treatment, etc. are performed on one side of the base material layer (adhesion surface with the release treatment layer). May be.
In addition, as a method for obtaining a release treatment layer by lamination, a release treatment agent is blended with a propylene-ethylene block copolymer (A) by an extruder and melted by heating, and the substrate layer is formed into a film form from a T-die. The base layer and the release treatment layer in which the release treatment agent is blended with the propylene-ethylene block copolymer (A) are heated and melted by a method of laminating on one side or an extruder, and a T-die together with the base layer. A method of co-extrusion into a film can be mentioned.
In the present invention, there is provided a method in which a release treatment layer obtained by blending a silicone-based or long-chain alkyl release treatment agent with a propylene-ethylene block copolymer (A) is coextruded in a film form from a T-die together with a base material layer. Adopting it is advantageous in terms of pollution and economy. Furthermore, it becomes the outstanding surface protection film with very few fish eyes.

The thickness of the release treatment layer is not particularly limited, but in the case of a method of forming a release treatment layer by applying a release treatment agent in a later step, the amount of the release treatment agent applied is usually 0 in the case of a silicone-based material. 0.01 to 10 g / m ² , preferably 0.5 to 0.7 g / m ² , and more preferably 0.1 to 0.4 g / m ² . In the case of long-chain alkyl-based, 0.005~10g / ^{m 2,} preferably 0.02~0.3g / ^{m 2,} particularly preferably preferably 0.01 to 0.1 g / ^{m 2.}
Moreover, in the case of the method of mix | blending a peeling agent with the propylene-ethylene block copolymer (A) for base material layers of this invention, and heat-melting from an extruder, in the method of forming normally, it is 0.1. It is 100 μm, preferably 1 to 50 μm, more preferably 5 to 30 μm, and most preferably 10 to 20 μm.

6). Applications of the surface protective film Applications of the surface protective film of the present invention include all known products that require surface protection. By field, for example, protective films for transporting electronic components and protective films for printed boards Electronics field such as window glass protective film, baking coating film, guard film for protecting automobiles to users, marking film for display, marking film for decoration, sponge film for buffering, protection, heat insulation and soundproofing, etc. Automotive field, medical and hygiene materials field such as adhesive bandages and transdermal patches, and electrical insulation, identification, duct construction, window glass protection, curing, packaging, packaging, office use, home use And housing / construction field such as protective film for fixing, bundling and repair.
Among these, it is particularly preferably used for surface protection of building members such as synthetic resin plates, decorative plates, metal plates and glass plates, and surface protection of liquid crystal display components such as polarizing plates and retardation plates. it can.

  Examples of the present invention will be specifically described below, but the present invention is not limited to these examples. The physical property measurement methods, characteristic evaluation methods, and resin materials used in Examples and Comparative Examples are as follows.

1. Physical property measurement method, characteristic evaluation method (1) MFR: A propylene-ethylene block copolymer was measured at 230 ° C. under a load of 21.18 N in accordance with JIS K-7210-1995.
(2) Density: Measured according to JIS K-6922-2: 1997 appendix (23 ° C.).
(3) Melting peak temperature: Using a differential scanning calorimeter (Seiko DSC), a sample amount of 5.0 mg was taken, held at 200 ° C. for 5 minutes, and then crystallized at a rate of temperature decrease of 10 ° C./min to 40 ° C. And the melting peak temperature (Tmp) when melted at a heating rate of 10 ° C./min was measured.
(4) Weight average molecular weight (Mw), number average molecular weight (Mn): measured by the method described in the description of the base material layer.

(5) TREF measurement of base layer resin: A sample is dissolved in o-dichlorobenzene (containing 0.5 mg / ml BHT) at 140 ° C. to obtain a solution. This is introduced into a 140 ° C. TREF column, cooled to 100 ° C. at a rate of 8 ° C./min, subsequently cooled to −15 ° C. at a rate of 4 ° C./min, and held for 60 minutes. Thereafter, o-dichlorobenzene (containing 0.5 mg / ml BHT) as a solvent is caused to flow through the column at a flow rate of 1 ml / min, and components dissolved in o-dichlorobenzene at −15 ° C. in the TREF column. Elution is performed for 10 minutes, and then the column is linearly heated to 140 ° C. at a heating rate of 100 ° C./hour to obtain an elution curve. (A) Apparatus (A-1) TREF part TREF column: 4.3 mmφ × 150 mm stainless steel column Column packing material: 100 μm Surface inactive glass beads )
Temperature distribution: ± 0.5 ° C
Temperature controller: Chino Corporation Digital Program Controller KP1000 (Valve Oven)
Heating method: Air bath oven Measurement temperature: 140 ° C
Temperature distribution: ± 1 ° C
Valve: 6-way valve 4-way valve (b-2) Sample injection part injection method: loop injection method Injection amount: loop size 0.1 ml
Inlet heating method: Aluminum heat block measurement temperature: 140 ° C
(I-3) Detector detector: fixed wavelength infrared detector MIRAN 1A manufactured by FOXBORO
Detection wavelength: 3.42 μm
High-temperature flow cell: Micro flow cell for LC-IR Optical path length: 1.5 mm Window shape: 2φ x 4 mm long circle Synthetic sapphire window measurement temperature: 140 ° C
(A-4) Pump unit liquid feed pump: SSC-3461 pump (b) manufactured by Senshu Kagaku Co., Ltd. (b) Measurement conditions Solvent: o-dichlorobenzene (including 0.5 mg / ml BHT)
Sample concentration: 5 mg / ml
Sample injection volume: 0.1 ml
Solvent flow rate: 1 ml / min

(6) Measurement of solid viscoelasticity A sample cut into a strip shape of 10 mm width × 18 mm length × 2 mm thickness from a 2 mm thick sheet injection-molded under the following conditions was used. The apparatus used was ARES manufactured by Rheometric Scientific. The frequency is 1 Hz. The measurement temperature was raised stepwise from −60 ° C., and the measurement was performed until the sample melted and became impossible to measure. The strain was performed in the range of 0.1 to 0.5%.
Test piece preparation conditions Standard number: JIS-7152 (ISO294-1)
Molding machine: TU-15 injection molding machine manufactured by Toyo Machine Metal Co., Ltd. Molding machine set temperature: 80, 80, 160, 200, 200, 200 ° C. from below the hopper
Mold temperature: 40 ℃
Injection speed: 200 mm / sec (speed in the mold cavity)
Injection pressure: 800 kgf / cm ²
Holding pressure: 800 kgf / cm ²
Holding time: 40 seconds
Mold shape: Flat plate (2mm thickness, 30mm width, 90mm length)
(7) Intrinsic viscosity (synonymous with intrinsic viscosity) of normal temperature xylene soluble component (CXS)
A 2 g sample is dissolved in 300 ml of p-xylene (containing 0.5 mg / ml BHT) at 130 ° C. to make a solution, and then left at 23 ° C. for 12 hours. Thereafter, the precipitated polymer is filtered off, p-xylene is evaporated from the filtrate, and further dried under reduced pressure at 100 ° C. for 12 hours, and CXS is collected and weighed. The intrinsic viscosity of the obtained CXS component was measured at 135 ° C. using Decalin as a solvent using an Ubbelohde viscometer.
(8) Calculation of ethylene content It measured by the method described by description of the base material layer.

(9) Haze: The film was conditioned at 23 ° C. and 50% RH for 24 hours, and then measured with a haze meter according to JIS-K7136-2000.
The smaller the value obtained, the better the transparency.
(10) Tensile elastic modulus: The film was measured for tensile elastic modulus in the flow direction (MD) under the following conditions in accordance with ISO 527.
The higher the obtained numerical value, the higher the rigidity of the film and the easier it is to handle it as a surface protecting film.
Sample length: 150mm
Sample width: 10mm
Distance between chucks: 100mm
Crosshead speed: 25mm / min
(11) Fish eye: The film was cut into a size of 20 cm × 15 cm, five films were visually observed, the number of fish eyes was counted, and the number per 1 m ^{2 of} area was calculated. The size of the fish eye is 0.4 mm or more in the major axis (≧ 0.4 mm), 0.2 mm or less smaller than 0.4 mm (<0.4 mm to ≧ 0.2 mm), 0.1 mm or larger smaller than 0.2 mm (< 0.2 mm to ≧ 0.1 mm), and the number of each was divided (unit: pieces / m ² ).
When the number of fish eyes is small, even if the surface protective film is attached to the object to be protected and stacked and stored, the object to be protected does not dent, and is better as the surface protective film.
(12) Tackiness: Acrylic resin plate (mirror surface acrylic plate (manufactured by Mitsubishi Rayon Co., Ltd. LIGHT L001 ”3 mm plate) After aging the pasted film at a temperature of 23 ° C. and a humidity of 50% for 12 hours, in accordance with JIS Z0237, at a pulling speed of 300 mm / min, at a peeling angle of 180 ° C. The adhesive strength per 25 mm width was measured.
The higher the value, the higher the adhesive strength. Although the target strength varies depending on the non-adherent body, the adhesive strength is generally used in the range of 1 to 400 g / 25 mm. If the adhesive strength is too low, bonding to the adherend cannot be performed. If the adhesive strength is too high, it cannot be easily peeled off from the adherend.
(13) Peeling treatment layer-adhesive delamination property: Usually, the surface protective film is wound around a paper tube in a form in which the peeling treatment layer and the pressure sensitive adhesive layer are in contact with each other, fed out, and adhered to a product. As an evaluation of unwinding property, the molded film is rolled up in a form in which a release treatment layer and an adhesive layer are in contact with a 3-inch paper tube. When mounted on the unwinding machine, it is smooth without wrinkles or sagging. It was visually confirmed whether it could be fed out smoothly, and ○ that could be smoothly fed out was marked with ○, and that that could not be smoothly fed out was marked with ×.
(14) Contamination resistance of adherend: In the above-described adhesion evaluation, when the film is peeled off from the acrylic plate, ○ indicates that no peeling trace remains, and the peeling trace or adhesive layer resin remains on the acrylic plate. X.

2. Resin Material (1) Base Layer Resin As the propylene-ethylene block copolymer of the base layer resin, the propylene-ethylene block copolymers (PEB-1 to 9) obtained in Production Examples 1 to 9 described later are used. It was. The polymerization conditions and polymerization results are shown in Table 3, and the physical properties are shown in Table 4.

(Production Example 1)
(I) Preparation of prepolymerization catalyst (a) Chemical treatment of silicate In a 10-liter glass separable flask equipped with a stirring blade, 3.75 liters of distilled water, followed by 2.5 kg of concentrated sulfuric acid (96%) Slowly added. At 50 ° C., 1 kg of montmorillonite (Menzawa Chemical Co., Ltd. Benclay SL; average particle size = 25 μm, particle size distribution = 10-60 μm) was dispersed, heated to 90 ° C., and maintained at that temperature for 6.5 hours. After cooling to 50 ° C., the slurry was filtered under reduced pressure to recover the cake. 7 liters of distilled water was added to this cake to reslurry it, and then filtered. This washing operation was performed until the pH of the washing solution (filtrate) exceeded 3.5. The collected cake was dried at 110 ° C. overnight under a nitrogen atmosphere. The weight after drying was 707 g.
(B) Drying of silicate The silicate previously chemically treated was dried with a kiln dryer. Specifications and drying conditions are as follows.
Rotating cylinder: Cylindrical inner diameter 50 mm Heating zone 550 mm (Electric furnace) Speed with rotating blade: 2 rpm Tilt angle: 20/520 Silicate feed rate: 2.5 g / min Gas flow rate: Nitrogen 96 liters / hour Countercurrent drying Temperature: 200 ° C (powder temperature)
(C) Preparation of catalyst An autoclave having an internal volume of 16 liters having a stirring and temperature control device was sufficiently substituted with nitrogen. To this, 200 g of dry silicate was introduced, 1,160 ml of mixed heptane and 840 ml of a heptane solution of triethylaluminum (0.60 M) were added and stirred at room temperature. After 1 hour, the mixture was washed with mixed heptane to prepare 2,000 ml of silicate slurry. Next, 9.6 ml of a heptane solution of triisobutylaluminum (0.71 ML) was added to the silicate slurry prepared above and reacted at 25 ° C. for 1 hour. In parallel, 187 ml of (r) -dichloro [1,1′-dimethylsilylenebis {2-methyl-4- (4-chlorophenyl) -4H-azurenyl}] zirconium and 2,180 mg (0.3 mM) of mixed heptane Then, 33.1 ml of a heptane solution of triisobutylaluminum (0.71 M) was added and the mixture reacted at room temperature for 1 hour was added to the silicate slurry. After stirring for 1 hour, 5,000 ml was added with mixed heptane. Prepared.
(D) Preliminary polymerization / washing Subsequently, the temperature in the tank was raised by 40 ° C., and when the temperature was stabilized, propylene was supplied at a rate of 100 g / hour to maintain the temperature. After 4 hours, the supply of propylene was stopped and maintained for another 2 hours.
After completion of the prepolymerization, the remaining monomer was purged, the stirring was stopped and the mixture was allowed to stand for about 10 minutes, and then the supernatant was decanted to 2,400 ml. Subsequently, 9.5 ml of a heptane solution of triisobutylaluminum (0.71 ML) and 5600 ml of mixed heptane were further added, stirred at 40 ° C. for 30 minutes, allowed to stand for 10 minutes, and then 5600 ml of the supernatant was removed. This operation was further repeated 3 times. When the component analysis of the final supernatant was performed, the concentration of the organoaluminum component was 1.23 mmol / liter, the Zr concentration was 8.6 × 10 −6 g / L, and the abundance in the supernatant relative to the charged amount was It was 0.016%. Subsequently, 170 ml of a heptane solution of triisobutylaluminum (0.71 ML) was added, followed by drying at 45 ° C. under reduced pressure. A prepolymerized catalyst containing 2.0 g of polypropylene per 1 g of catalyst was obtained.

(Ii) First Step In the first step, propylene-ethylene random copolymerization was carried out using a liquid phase polymerization tank with an agitator having an internal volume of 0.4 m ³ . Liquefied propylene, liquefied ethylene, and triisobutylaluminum were continuously fed at 90 kg / hour, 4.2 kg / hour, and 21.2 g / hour, respectively. The hydrogen supply amount was adjusted so that the MFR in the first step became a target value.
Further, the above prepolymerized catalyst was supplied as a catalyst (excluding the weight of the prepolymerized polymer) so as to be 6.9 g / hour. The polymerization tank was cooled so that the polymerization temperature was 45 ° C.
When the propylene-ethylene random copolymer obtained in the first step was analyzed, BD (bulk density) was 0.46 g / cc, MFR was 7.0 g / 10 min, and ethylene content was 3.7 wt%. .

(Iii) Second Step In the second step, propylene-ethylene random copolymerization was carried out using a stirred gas phase polymerization tank having an internal volume of 0.5 m ³ . The slurry containing polymer particles was continuously withdrawn from the liquid phase polymerization tank in the first step, flushed with liquefied propylene, and then pressurized with nitrogen and continuously supplied to the gas phase polymerization tank.
The polymerization tank was controlled so that the temperature was 80 ° C. and the total partial pressure of propylene, ethylene, and hydrogen was 1.5 MPa. At that time, the concentration of propylene, ethylene and hydrogen in the total partial pressure of propylene, ethylene and hydrogen was controlled to be 66.97 vol%, 32.99 vol% and 420 volppm, respectively.
Furthermore, ethanol was supplied to the gas phase polymerization tank as an activity inhibitor. The supply amount of ethanol was set to 0.3 mol / mol with respect to aluminum in TIBA supplied along with the polymer particles supplied to the gas phase polymerization tank.
When the propylene-ethylene block copolymer thus obtained was analyzed, the activity was 8.7 kg / g-catalyst, the BD was 0.41 g / cc, the MFR was 7.0 g / 10 min, and the ethylene content was 8.7 wt. %Met.

(Iv) Granulation The following antioxidant was added to the blender to the block copolymer powder obtained above, and the mixture was sufficiently stirred and mixed.
Antioxidant: Tetrakis [methylene-3- (3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate] methane (manufactured by Ciba Specialty Chemicals Co., Ltd., Irganox 1010) 0.05 Part by weight, Tris (2,4-di-t-butylphenyl) phosphite (manufactured by Ciba Specialty Chemicals Co., Ltd., Irgafos 168) 0.10 part by weight Copolymer powder added with additives is added to a Henschel mixer. After mixing at 750 rpm for 1 minute at room temperature with a PCM twin screw extruder manufactured by Ikegai Seisakusho with a screw diameter of 30 mm, the mixture is melt-kneaded at a screw rotation speed of 200 rpm, a discharge rate of 10 kg / hr, and an extruder temperature of 190 ° C. The molten resin extruded from is taken out while being cooled and solidified in a cooling water tank, and a strand cutter is removed. The strand was cut into a diameter of about 2 mm and a length of about 3 mm to obtain a propylene-ethylene block copolymer raw material pellet (PEB-1).

(Production Example 2)
(I) 1st process The horizontal reactor (L / D = 6, internal volume 100 liters) which has a stirring blade was fully dried, and the inside was fully substituted with nitrogen gas. In the presence of a polypropylene powder bed, a prepolymerized catalyst prepared by the same method as in Production Example 1 was added to the upstream part of the reactor while stirring at a rotation speed of 30 rpm (as a solid catalyst amount excluding the prepolymerized powder). 444 g / hr, triisobutylaluminum was continuously supplied at 15.0 mmol / hr. The monomer mixed gas is continuously reacted so that the reactor temperature is maintained at 65 ° C., the pressure is maintained at 2.00 MPaG, the ethylene / propylene molar ratio in the gas phase in the reactor is 0.058, and the hydrogen concentration is 150 ppm. It was made to distribute | circulate in a container and vapor phase polymerization was performed. The polymer powder produced by the reaction was continuously extracted from the downstream portion of the reactor so that the amount of the powder bed in the reactor was constant. At this time, the amount of the polymer extracted when the steady state was reached was 10.0 kg / hr.
When the propylene-ethylene random copolymer obtained in the first step was analyzed, BD (bulk density) was 0.47 g / cc, MFR was 9.0 g / 10 min, and ethylene content was 1.7 wt%. .
(Ii) Second Step The propylene-ethylene copolymer extracted from the first step was continuously supplied to a horizontal reactor (L / D = 6, internal volume 100 liters) having a stirring blade. While stirring at a rotation speed of 25 rpm, the temperature of the reactor is maintained at 70 ° C., the pressure is maintained at 1.88 MPaG, the ethylene / propylene molar ratio in the gas phase portion in the reactor is 0.450, and the hydrogen concentration is 300 ppm. A monomer mixed gas was continuously passed through the reactor to carry out gas phase polymerization. The polymer powder produced by the reaction was continuously extracted from the downstream portion of the reactor so that the amount of the powder bed in the reactor was constant. At this time, oxygen was supplied as an activity inhibitor so that the amount of polymer extracted was 18.0 kg / hr, and the polymerization reaction amount in the second step was controlled.
When the propylene-ethylene block copolymer thus obtained was analyzed, the activity was 40.5 kg / g-catalyst, BD was 0.48 g / cc, MFR was 7.0 g / 10 min, and the ethylene content was 6.3 wt. %Met.
From the obtained polymer powder, (PEB-2) raw material pellets were obtained under the same additive formulation and granulation conditions as in Production Example 1.

(Production Examples 3 to 7)
In the same manner as in Production Example 1, the polymerization conditions were changed to produce a propylene-ethylene block copolymer.
From the obtained polymer powder, (PEB-3 to 7) raw material pellets were obtained by the same additive formulation and granulation conditions as in Production Example 1.

(Production Example 8)
(I) Preparation of solid catalyst component 2,000 ml of dehydrated and deoxygenated n-heptane was introduced into a fully nitrogen-substituted flask, and then 2.6 mol of MgCl ₂ and Ti (On-C ₄ H) were introduced. ₉ ) 5.2 mol of ₄ was introduced and reacted at 95 ° C. for 2 hours. After completion of the reaction, the temperature was lowered to 40 ° C., and then 320 ml of methylhydropolysiloxane (20 centistokes) was introduced and reacted for 3 hours. The resulting solid component was washed with n-heptane.
Next, 4,000 milliliters of n-heptane purified in the same manner as described above was introduced into a sufficiently nitrogen-substituted flask, and 1.46 mol of the solid component synthesized above was introduced in terms of Mg atoms. Next, 25 ml of n-heptane was mixed with 2.62 mol of SiCl ₄ , introduced into the flask at 30 ° C. for 30 minutes, and reacted at 70 ° C. for 3 hours. After completion of the reaction, washing with n-heptane was performed. Next, 0.15 mol of phthalic acid chloride was mixed with 25 ml of n-heptane, introduced into the flask at 70 ° C. for 30 minutes, and reacted at 90 ° C. for 1 hour. After completion of the reaction, washing with n-heptane was performed. Next, 11.4 mol of TiCl ₄ was introduced and reacted at 110 ° C. for 3 hours. After completion of the reaction, the solid component was obtained by washing with n-heptane. The titanium content of this solid component was 2.0 wt%.
Next, an autoclave having an internal volume of 16 liters having a stirring and temperature control device was sufficiently replaced with nitrogen, and 5,000 milliliters of n-heptane purified in the same manner as above was introduced into the autoclave to synthesize the solid component synthesized above. Gram was introduced, and 0.875 mol of SiCl ₄ was introduced and reacted at 90 ° C. for 2 hours. After completion of the reaction, further (CH ₂ ═CH) Si (CH ₃ ) ₃ 0.15 mol, (t-C ₄ H ₉ ) (CH ₃ ) Si (OCH ₃ ) ₂ 0.075 mol and Al (C ₂ H ₅ ) ₃ 0.4 mol was sequentially introduced and contacted at 30 ° C. for 2 hours. After completion of the contact, the catalyst was thoroughly washed with n-heptane to obtain a solid catalyst component mainly composed of magnesium chloride. The titanium content of this product was 1.8 wt%.
(Ii) Prepolymerization An autoclave having an internal volume of 16 liters equipped with a stirring and temperature control device was sufficiently replaced with nitrogen. To this, 100 g of the n-heptane slurry of the solid catalyst component prepared above was introduced as a solid catalyst component, and n-heptane was further introduced to adjust the liquid level to 5,000 ml. Next, the temperature in the tank was adjusted to 15 ° C., and 0.1 mol of triethylaluminum / n-heptane solution (10 wt%) was added as Al (C ₂ H ₅ ) ₃ . Thereafter, prepolymerization was performed by supplying propylene at a rate of 50 g / hour for 2 hours. After completion of the prepolymerization, the residual monomer was purged and the solid catalyst was thoroughly washed with n-heptane. After the washing, drying under reduced pressure was performed to obtain a prepolymerized catalyst. The prepolymerized catalyst contained 2.0 g of polypropylene per 1 g of the catalyst.
(Iii) Polymerization Production Example except that the prepolymerized catalyst thus obtained was used, and triethylaluminum was continuously fed at 10 g / hour instead of triisobutylaluminum, and the polymerization conditions shown in Table 3 were used. In the same manner as in No. 1, a propylene-ethylene block copolymer was produced.
From the obtained polymer powder, (PEB-8) raw material pellets were obtained by the same additive formulation and granulation conditions as in Production Example 1.

(Production Example 9)
In Production Example 1, polymerization was carried out in the same manner as in Polymerization Production Example 1 except that only the first step was carried out without carrying out the second step, and a propylene-ethylene random copolymer was produced.
From the obtained polymer powder, (PEB-9) raw material pellets were obtained by the same additive formulation and granulation conditions as in Production Example 1.

(2) Adhesive layer As the acrylic adhesive used as the adhesive layer, the adhesive solutions (S-1) to (S-3) prepared as follows were used. As a comparative example, Novatec EVA / LV342 (manufactured by Nippon Polyethylene Co., Ltd.) having a vinyl acetate content (VAC) of 10% obtained by a high-pressure radical polymerization method was used as an ethylene / vinyl acetate copolymer (EVA).

Preparation of acrylic pressure-sensitive adhesive solution (S-1) In ethyl acetate, 100 parts by weight of 2-ethylhexyl acrylate and 4 parts by weight of 2-hydroxyethyl acrylate were copolymerized so as to be 35% on a monomer basis, and the weight average molecular weight. A solution containing 600,000 acrylic polymers was obtained. Into this solution, 4 parts by weight of an isocyanate-based cross-linking agent having an isocyanurate ring (manufactured by Nippon Polyurethane Industry Co., Ltd., Coronate HX) is blended with 100 parts by weight of an acrylic polymer (dry weight), and ethyl acetate is further added to form a solid. An acrylic pressure-sensitive adhesive solution (S-1) having a partial concentration adjusted to 20% was prepared.

Preparation of acrylic pressure-sensitive adhesive solution (S-2) In ethyl acetate, 100 parts by weight of 2-ethylhexyl acrylate and 3 parts by weight of acrylic acid were copolymerized so as to be 35% on a monomer basis, and the weight average molecular weight was 500,000. A solution containing an acrylic polymer was obtained. To this solution, 4 parts by weight of an epoxy crosslinking agent (Mitsubishi Gas Co., Ltd., Tetrad C) is blended with 100 parts by weight of an acrylic polymer (dry weight), and ethyl acetate is added to make the solid content concentration 20%. An adjusted acrylic pressure-sensitive adhesive solution (S-2) was prepared.

Preparation of acrylic pressure-sensitive adhesive solution (S-3) In ethyl acetate, 100 parts by weight of 2-ethylhexyl acrylate and 3 parts by weight of acrylic acid were copolymerized so as to be 35% on a monomer basis, and the weight average molecular weight was 500,000. A solution containing an acrylic polymer was obtained. In this solution, 100 parts by weight of an acrylic polymer (dry weight), 4 parts by weight of an epoxy crosslinking agent (Mitsubishi Gas Chemical Co., Ltd., Tetrad C) and an isocyanate crosslinking agent (manufactured by Nippon Polyurethane Industry Co., Ltd., An acrylic pressure-sensitive adhesive solution (S-3) was prepared by adding 1 part by weight of Coronate L) and further adding ethyl acetate to adjust the solid content concentration to 20%.

(3) Release treatment layer As the release treatment layer, as a silicone release agent, X-62-2378 (manufactured by Shin-Etsu Chemical Co., Ltd.), polydimethylsiloxane SH200 (manufactured by Dow Corning Toray), three-dimensional organopoly X-92-140 (manufactured by Shin-Etsu Chemical Co., Ltd.) was used as the siloxane, and Pyroyl 101 (manufactured by Yushi Co., Ltd.) was used as the long-chain alkyl release agent.

Example 1
As a base material layer, PEB-1 was formed using a T-die molding machine having an extruder 35 mmφ, an air knife and a cooling roll at a molding temperature of 230 ° C. and a cooling roll temperature of 30 ° C., with a base layer thickness of 40 μm. A single layer film was prepared. On one surface of the base layer of the obtained single layer film, an acrylic pressure-sensitive adhesive solution (S-1) was used as an adhesive layer, applied with a reverse coater, and dried in a drying oven at 100 ° C. for 2 minutes. Then, an acrylic pressure-sensitive adhesive layer having a thickness of 10 μm was formed. Furthermore, a three-dimensional organopolyethylene is added to a toluene solution (solid content 30%) of X-62-2378 (manufactured by Shin-Etsu Chemical Co., Ltd.) as an addition-type silicone release agent on the other surface of the adhesive layer of the base material layer. As a siloxane, 0.38 g of a solution obtained by mixing a toluene / xylene solution (solid content 30%) of X-92-140 (manufactured by Shin-Etsu Chemical Co., Ltd.) so that the three-dimensional organopolysiloxane content is 30%. After coating so as to be / m ² , a surface protective film having a release treatment layer formed by heat treatment at 120 ° C. for 1 minute was produced. Table 5 shows the evaluation results of the obtained surface protective film.

(Example 2)
Evaluation was performed by forming a film by the same method as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-2. The results are shown in Table 5.

(Example 3)
Evaluation was performed by forming a film in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-3. The results are shown in Table 5.

Example 4
A film was formed and evaluated in the same manner as in Example 2 except that the pressure-sensitive adhesive solution used in Example 2 was replaced with an acrylic pressure-sensitive adhesive solution (S-2). The results are shown in Table 5.

(Example 5)
A film was formed and evaluated in the same manner as in Example 2 except that the pressure-sensitive adhesive solution used in Example 2 was replaced with an acrylic pressure-sensitive adhesive solution (S-3). The results are shown in Table 5.

(Example 6)
A film was formed and evaluated in the same manner as in Example 2 except that the thickness of the pressure-sensitive adhesive layer used in Example 2 was changed to 20 μm. The results are shown in Table 5.

(Example 7)
Except that the release treatment agent used in Example 2 was replaced with a layer formed by applying a 2% toluene solution of Pyroyl 101 (manufactured by Yushi Co., Ltd.) as a long-chain alkyl release treatment agent. The film was formed by the same method as in Example 1 and evaluated. In addition, the processing method apply | coated 2% toluene solution of Pyroyl 101 (made on the other hand company oil and fat Co., Ltd.) so that it might become 0.02 g / m < ² >, and heat-processed at 80 degreeC x 1 minute, and formed the peeling process layer. The results are shown in Table 5.

(Example 8)
PEB-2 as the base material layer, acrylic pressure-sensitive adhesive solution (S-1) as the pressure-sensitive adhesive layer, 99.75% by weight of PEB-2 as the release treatment layer and polydimethylsiloxane SH200 (Toray as the silicone-based release agent) -A 0.25 wt% melt-extruded mixed composition was used.
Extruder 35 mmφ for the base material layer, 20 mmφ for the exfoliation treatment layer, a two-layer T-die molding machine having an air knife and a cooling roll, using a molding temperature of 230 ° C. and a cooling roll temperature of 30 ° C. A co-pressed two-layer film made of a two-layer T-die film having a thickness of 30 μm and an adhesive layer thickness of 10 μm was prepared. Using the acrylic adhesive solution (S-1) on the surface opposite to the release treatment layer of the base layer of the obtained two-layer film, it was applied with a reverse coater and dried at 100 ° C. for 2 minutes in a drying oven. The surface protective film which dried and formed the 10-micrometer-thick acrylic adhesive layer was produced. Table 5 shows the evaluation results of the obtained surface protective film.

(Comparative Example 1)
A film was formed and evaluated in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-4. The results are shown in Table 6.

(Comparative Example 2)
A film was formed and evaluated in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-5. The results are shown in Table 6.

(Comparative Example 3)
A film was formed and evaluated in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-6. The results are shown in Table 6.

(Comparative Example 4)
A film was formed and evaluated in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-7. The results are shown in Table 6.

(Comparative Example 5)
A film was formed and evaluated in the same manner as in Example 1 except that the base layer resin PEB-1 used in Example 1 was replaced with PEB-8. The results are shown in Table 6.

(Comparative Example 6)
A film was formed and evaluated in the same manner as in Example 1 except that the base material layer resin PEB-1 used in Example 1 was replaced with PEB-9. The results are shown in Table 6.

(Comparative Example 7)
PEB-2 as the base material layer, Novatec EVA / LV342 (made by Nippon Polyethylene Co., Ltd.) having a vinyl acetate content (VAC) of 10% as the adhesive layer, and an addition-type silicone-based release as the release treatment layer X-62-2378 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a solution in a toluene solution (solid content 30%) and a three-dimensional organopolysiloxane as a 3-dimensional organopolysiloxane in toluene / xylene solution (solid) 30%) was used so that the content of the three-dimensional organopolysiloxane was 30%.
Extruder 35 mmφ for substrate layer, 20 mmφ for adhesive layer, multilayer T-die molding machine with air knife and cooling roll, forming temperature 230 ° C, cooling roll temperature 30 ° C, substrate layer thickness 40 µm A co-pressed two-layer film composed of a two-layer T-die film having an adhesive layer thickness of 10 μm was prepared. On the surface opposite to the adhesive layer of the base layer of the obtained two-layer film, a toluene solution (solid content 30%) of X-62-2378 (manufactured by Shin-Etsu Chemical Co., Ltd.) as an addition type silicone release agent. A solution prepared by mixing a toluene / xylene solution (solid content 30%) of X-92-140 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a three-dimensional organopolysiloxane so that the three-dimensional organopolysiloxane content is 30%. Was applied so as to be 0.38 g / m ² , followed by heat treatment at 120 ° C. for 1 minute to prepare a surface protective film on which a release treatment layer was formed. Table 6 shows the evaluation results of the obtained surface protective film.

(Comparative Example 8)
X-92-140 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a three-dimensional organopolysiloxane in a toluene solution (solid content 30%) of X-62-2378 (manufactured by Shin-Etsu Chemical Co., Ltd.) of the release treatment layer used in Example 2. ) In a toluene / xylene solution (solid content 30%) mixed so that the three-dimensional organopolysiloxane content is 30%, the coating amount is changed from 0.38 g / m ² to 12 g / m ² Except for the above, a film was formed in the same manner as in Example 2 and evaluated. The results are shown in Table 6.

(Comparative Example 9)
Except for the use of 100% by weight of PEB-2 without using the silicone release agent of the mixed composition of PEB-2 of the release treatment layer and the silicone release agent (polydimethylsiloxane SH200) used in Example 8. Films were formed in the same manner as in Example 8 and evaluated. The results are shown in Table 6.

From the results of Table 5 and Table 6, it can be seen that the surface protective film of the present invention is excellent in transparency and flexibility and has few fish eyes (Examples 1 to 8). On the other hand, when the ethylene content of the propylene-ethylene random copolymer component (A2) is increased, the compatibility with the propylene-ethylene random copolymer component (A1) is poor (glass transition temperature is a double peak) and transparent. The properties deteriorate (Comparative Example 1). Further, when the amount of the propylene-ethylene random copolymer component (A2) is too large, the feeding property and adherend contamination resistance are deteriorated (Comparative Example 2), and when the amount is too small, the rigidity becomes too high and the flexibility is lowered. (Comparative Example 6) Further, when the MFR of the propylene-ethylene block copolymer used for the base material layer is outside the range of the present invention, the film-forming property of the film is not stable, or shark skin is generated (Comparative Examples 3 to 4). ). Moreover, when the propylene-ethylene block copolymer manufactured except the metallocene catalyst is used for the base material layer, fish eyes increase and the appearance deteriorates (Comparative Example 5).
In addition, by using an acrylic pressure-sensitive adhesive for the pressure-sensitive adhesive layer, it is possible to provide a film for surface protection that has high adhesive strength and is excellent in stain resistance to an adherend (Examples 1 to 8). On the other hand, a film using EVA for the pressure-sensitive adhesive layer instead of an acrylic pressure-sensitive adhesive layer has low adhesive strength and poor stain resistance to the adherend (Comparative Example 7).
Moreover, even if the adhesive strength is strong, the peelability between the outer layer and the adhesive layer is improved by using a silicone-based or long-chain alkyl-based release treatment agent in the release treatment layer, and the pay-out property is improved (Examples 1 to 8). On the other hand, a film that does not use a silicone-based or long-chain alkyl-based release treatment agent in the release treatment layer has poor drawability (Comparative Example 9). Moreover, when there is too much quantity of the silicone type or long-chain alkyl type release processing agent of a peeling process layer, the stain resistance to a to-be-adhered body will be inferior (Comparative Example 8).

  The surface protective film of the present invention uses a specific propylene-ethylene block copolymer as a base layer, an acrylic pressure-sensitive adhesive as an adhesive layer, and a silicone-based or long-chain alkyl-based release treatment agent as a release treatment layer. As it is used, there are very few unmelted fish eyes at the time of film molding, and even if the surface protection film is stuck on the object to be stacked and stored, the object to be protected does not have a dent and is transparent. Excellent flexibility, and excellent stain resistance to the adherend. Furthermore, since a silicone-based or long-chain alkyl-based release treatment agent is used for the release treatment layer, when the roll is unwound from the roll winding state where both the adhesive layer and the release treatment layer are in contact with each other in a solid state, it is used. Sometimes it can be used as a surface protective film having the property of improving the feeding performance, and for protecting the surface of building members such as synthetic resin plates, decorative plates, metal plates, glass plates, and liquid crystals such as polarizing plates and retardation plates. It can be suitably used as a film for protecting the surface of the constituent member of the display.

It is a figure which shows the elution amount by TREF, and elution amount integration.

Claims (7)

In the surface protective film in which the adhesive layer is formed on one surface of the base material layer and the release treatment layer is formed on the other surface, the base material layer is polymerized using a metallocene catalyst, and the following (a1) to (a3) Formed of a propylene-ethylene block copolymer (A) having the following characteristics, the pressure-sensitive adhesive layer is formed of an acrylic pressure-sensitive adhesive (B), and the release treatment layer is a silicone-based or long-chain alkyl release treatment agent (C) When the release treatment layer is formed by applying a silicone-based or long-chain alkyl release treatment agent (C) in a later step, the application amount of the release treatment agent (C) is 10 g / m ² or less. A film for surface protection , which is characterized in that
(A) Propylene-ethylene block copolymer (a1) Using a metallocene-based catalyst, 30 to 95% by weight of propylene alone or propylene-ethylene random copolymer component (A1) in the first step, component in the second step Propylene-ethylene block copolymer (a2) obtained by sequential polymerization of 70 to 5% by weight of propylene-ethylene random copolymer component (A2) containing more ethylene than (A1) Melt flow rate (MFR: 230 ° C. 2.16 kg) is 1-30 g / 10 min. (A3) In the temperature-loss tangent (tan δ) curve obtained by solid viscoelasticity measurement (DMA), the tan δ curve has a single peak at 0 ° C. or lower. The film for surface protection according to claim 1, wherein the propylene-ethylene block copolymer (A) further satisfies the following (a4).
(A4) The component amount W (Mw ≦ 5,000) having a molecular weight of 5,000 or less obtained by gel permeation chromatography (GPC) is 0.8% by weight or less of the total. The film for surface protection according to claim 1 or 2, wherein the propylene-ethylene block copolymer (A) further satisfies the following (a5) to (a6).
(A5) The component (A1) obtained in the first step is a propylene-ethylene random copolymer having an ethylene content in the range of 0.5 to 6% by weight, and the proportion of the entire block copolymer is 30 to 85. In the range of% by weight, the component (A2) obtained in the second step has an ethylene content of 6 to 15% by weight more than (A1), and the ratio of the whole block copolymer is 70 to 15% by weight. (A6) It is obtained as a plot of the elution amount (dWt% / dT) against temperature by the temperature rising elution fractionation method (TREF) in the temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent. In the TREF elution curve, the peak temperature T (A1) observed on the high temperature side is in the range of 55 ° C. to 96 ° C., and the peak temperature T (A2) observed on the low temperature side is 45 ° C. or lower, or Over peak temperature T (A2) is not observed, propylene - the temperature T to 99 wt% of the ethylene block copolymer is eluted (A4) is 98 ° C. or less The film for surface protection according to any one of claims 1 to 3, wherein the propylene-ethylene block copolymer (A) further satisfies the following (a7) to (a8).
(A7) The component (A1) obtained in the first step is a propylene-ethylene random copolymer having an ethylene content in the range of 1.5 to 6% by weight, and the proportion of the whole block copolymer is 30 to 70. In the range of% by weight, the component (A2) obtained in the second step has an ethylene content of 8 to 15% by weight more than (A1), and the ratio of the whole block copolymer is in the range of 70 to 30% (A8) It is obtained as a plot of the elution amount (dWt% / dT) against temperature by the temperature rising elution fractionation method (TREF) in the temperature range of −15 ° C. to 140 ° C. using an o-dichlorobenzene solvent. In the TREF elution curve, the peak temperature T (A1) observed on the high temperature side is in the range of 60 ° C. to 88 ° C., and the peak temperature T (A2) observed on the low temperature side is 40 ° C. or lower, or Over peak temperature T (A2) is not observed, propylene - the temperature T to 99 wt% of the ethylene block copolymer is eluted (A4) is 90 ° C. or less The film for surface protection according to any one of claims 1 to 4, wherein the propylene-ethylene block copolymer (A) further satisfies the following (a9).
(A9) Intrinsic viscosity [η] cxs measured in 135 ° C. decalin of 23 ° C. xylene solubles is 1 to 2 dl / g   It is used for surface protection of building members, such as a synthetic resin board, a decorative board, a metal plate, and a glass plate, The film for surface protection of any one of Claims 1-5 characterized by the above-mentioned.   The film for surface protection according to any one of claims 1 to 5, which is used for surface protection of liquid crystal display components such as a polarizing plate and a retardation plate.

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