DE102017221703A1 - Chemical-resistant polyacrylate and pressure-sensitive adhesive based thereon - Google Patents

Abstract

It is a question of providing a polyacrylate with high chemical resistance, which is suitable for use in pressure-sensitive adhesives. This is achieved with a polyacrylate, which is characterized in that the polyacrylate is due to the following monomer composition:
a) 25 to 70% by weight of at least one acrylic acid ester of the formula (I) CH ₂ = CH-C (O) OR ¹ (I), wherein R ^{1 is} a linear or branched alkyl group having 1 to 10 C atoms;
b) from 25 to 70% by weight of at least one acrylic acid ester of the formula (II) CH ₂ = CH-C (O) OR ² wherein R ^{2 is} an alkoxyalkyl radical having 2 to 5 C atoms; (II)
c) 0.5 to 10% by weight of at least one acrylate monomer of the formula (III) CH ₂ = CH-C (O) OR ³ (III), wherein R ^{3 is} an H atom or a hydroxyalkyl radical having 1 to 4 carbon atoms.
The invention further provides a pressure-sensitive adhesive comprising such a polymer, an adhesive tape with this pressure-sensitive adhesive and the use of the pressure-sensitive adhesive for the production of bonds in electronic, optical or precision mechanical devices.

Description

The invention relates to the technical field of polyacrylates, as they are often used as a base component in adhesives, especially in PSAs. More specifically, the invention relates to a polyacrylate having high resistance to chemicals and a pressure-sensitive adhesive composition containing such a polyacrylate.

With the spread of electronic devices, the fields of application of the same extend. This also results in growing demands on the installed components. For example, the development of body-worn electronic devices (so-called wearables), such as smart watches, has made it increasingly important that the adhesions used there have a high resistance to various chemicals and barely even after prolonged storage in various media do not lose their adhesive power. Similar requirements are increasingly being placed on other electronic devices such as smartphones, tablets, notebooks, cameras, video cameras, keyboards and touchpads.

Another area where chemical resistant bonds are important is the application of labels or labels in environments where contact with chemicals is possible, such as in engine compartments. Frequently, tamper-resistant labels also require high resistance to various chemicals. On various occasions, the use of polyacrylate-based PSAs has been described in this context.

So describes WO 2016/089687 A1 a pressure-sensitive adhesive composed of the reaction product of from 20 to 60% by weight of methyl acrylate; From 40 to 80% by weight of ethyl, propyl and / or butyl acrylate; 0.2 to 5 wt .-% of a functionalized acrylate monomer and a crosslinking agent derived.

WO 2017/132058 A1 discloses a pressure-sensitive adhesive composition comprising a polymer obtained by polymerizing i) 2-ethylhexyl acrylate, butyl acrylate, isooctyl acrylate, 2-propylheptyl acrylate, n-octyl acrylate, 2-ethylhexyl methacrylate, butyl methacrylate, isooctyl methacrylate, 2-propylheptyl methacrylate and / or n-octyl methacrylate; ii) acrylonitrile and / or methacrylonitrile; and iii) acrylic acid and / or methacrylic acid is formed.

DE 10 2015 215 247 A1 The object of the present invention is a pressure-sensitive adhesive composition comprising as base polymer at least one or more acrylonitrile-butadiene solid rubbers and tackifier resins, the proportion of tackifier resins being from 30 to 130 phr and the acrylonitrile content in the solid acrylonitrile-butadiene rubber (s) ) is between 10 and 30% by weight.

US 5,665,835 describes a high polar pressure-sensitive adhesive copolymer obtained by copolymerization of alkyl acrylate monomers having 4 to 8 C atoms in the alkyl group and 15 to 50% by weight of polar acrylic monomers functionalized with carboxy or methoxy groups.

There is a continuing need for polymers with high chemical resistance which are suitable for use in pressure-sensitive adhesives. The object of the present invention is to provide a polyacrylate which has these properties.

1. a) 25 bis 70 Gew.-% mindestens eines Acrylsäureesters gemäß der Formel (I) CH₂=CH-C(O)OR¹ (I), worin R¹ für eine lineare oder verzweigte Alkylgruppe mit 1 bis 10 C-Atomen steht;
2. b) 25 bis 70 Gew.-% mindestens eines Acrylsäureesters gemäß der Formel (II) CH₂=CH-C(O)OR² (II), worin R² für einen Alkoxyalkylrest mit 2 bis 5 C-Atomen steht;
3. c) 0,5 bis 10 Gew.-% mindestens eines Acrylatmonomers gemäß der Formel (III) CH₂=CH-C(O)OR³ (III), worin R³ für ein H-Atom oder einen Hydroxyalkylrest mit 1 bis 4 C-Atomen steht.

A first and general object of the invention, with which the above object is achieved, is a polyacrylate, which is characterized in that the polyacrylate is due to the following monomer composition:

1. a) 25 to 70% by weight of at least one acrylic acid ester of the formula (I) CH ₂ = CH-C (O) OR ¹ (I), wherein R ^{1 is} a linear or branched alkyl group having 1 to 10 C atoms;
2. b) from 25 to 70% by weight of at least one acrylic acid ester of the formula (II) CH ₂ = CH-C (O) OR ² (II), wherein R ^{2 is} an alkoxyalkyl radical having 2 to 5 C atoms;
3. c) 0.5 to 10% by weight of at least one acrylate monomer of the formula (III) CH ₂ = CH-C (O) OR ³ (III), wherein R ^{3 is} an H atom or a hydroxyalkyl radical having 1 to 4 carbon atoms.

As has been shown, such polymers have both the required chemical resistance and good pressure-sensitive adhesive properties and are therefore very suitable as a base material for corresponding PSAs.

In one embodiment, the polyacrylate of the present invention has a Hansen solubility parameter of polar interactions of 8.5 to 9.5, preferably 9.0 to 9.5.

A description of solubility parameters known in the literature is given by means of the one-dimensional Hildebrand parameter (δ). However, these one-dimensional δ values are subject to errors that are usually large in the case of polar compounds such as acrylates or those capable of undergoing hydrogen bonding, such as, for example, acrylic acid. Because the model of one-dimensional Hildebrand solubility parameters has only limited application, it has been further developed by Hansen ( Hansen Solubility Parameters: A User's Handbook, Second Edition; Charles M. Hansen; 2007 CRC Press; ISBN 9780849372483 ).

The Hansen solubility parameters widely used nowadays are three-dimensional solubility parameters. They consist of a disperse fraction (δ _d ), a fraction of polar interactions (δ _p ) and a contribution to the hydrogen bonds (δ _H ). With the Hildebrand parameter δ they are connected as follows: $${\mathrm{\delta }}^2={\mathrm{\delta }}_d^2+{\mathrm{\delta }}_p^2+{\mathrm{\delta }}_H^2$$

Δ _d , δ _p and δ _H can not be directly determined experimentally for polyacrylates, but can be calculated by means of increment systems. A common and also used in this writing - method is the after Stefanis / Panayiotou ( Prediction of Hansen Solubility Parameters with a New Group Contribution Method; Int. J. Thermophys. (2008) 29: 568-585 ; Emmanuel Stefanis, Costas Panayiotou):

To determine the Hansen solubility parameters for the polyacrylates, the solubility parameters of the components attributable to the individual monomers in the polymers, ie the repeating unit in a polymer chain (without the polymerizable double bond, instead taking into account a covalent σ bond, as in the polymer chain present) in accordance with the provision in the said document. In this case, a specific value for the disperse fraction (δ _d ), the proportion of polar interactions (δ _p ) and the hydrogen bond formation fraction (δ _H ) are tabulated for each group in the building block, see Prediction of Hansen Solubility Parameters with a New Group Contribution Method; Int. J. Thermophys. (2008), Tables 3 to 6, pages 578 to 582 ,

Examples:

Polyacrylic acid contains the repeating unit - [- CH ₂ -CHC (O) OH-] _n -;
according to the increment system of Stefanis / Panayiotou, the Hansen solubility parameters (a CH ₂ group, a CH group and a COOH group) for the corresponding building block are δ _d = 17.7, δ _p = 8.6 and δ _H = 11.1.

Polybutyl acrylate contains the repeating unit
- [- CH ₂ -CHC (O) O (CH ₂ ) ₃ CH ₃ -] _n -;
with four CH ₂ groups, a CH group, a COO group and a CH ₃ group, the Hansen solubility parameters for the corresponding building block are δ _d = 17.1, δ _p = 8.6 and δ _H = 6 ; 5.

After calculating the Hansen solubility parameters of the monomer building blocks, the determination of the corresponding Hansen solubility parameters of the polyacrylate copolymers can be carried out. The solubility parameters (δ _d , δ _p , δ _H ) for acrylate copolymers are determined from the molar fraction of the individual monomers (building blocks) of which the polyacrylate is composed, wherein the respective Hansen values with the molar fraction of the monomer building block multiplied in the copolymer and then the proportional parameters (δ _d , δ _p , δ _H for each monomer) are summed.

This is illustrated by the example of a polyacrylate consisting of 97% by weight of butyl acrylate and 3% by weight of acrylic acid, corresponding to a molar composition of 84.8% by mole of butyl acrylate and 5.2% by weight of acrylic acid. Table 1: Hansen solubility parameter calculation δ _d δ _p δ _H butyl acrylate 0.848 × 17.1 0.848 × 8.6 0.848 × 6.5 (δ _d = 17.1, δ _p = 8.6 and δ _H = 6.5) = 16.2 = 8.2 = 6.1 acrylic acid 0.052 × 17.7 0.052 × 8.6 0.052 × 11.1 (δ _d = 17.7, δ _p = 8.6 and δ _H = 11.1) = 0.9 = 0.4 = 0.6 + polyacrylate 17.1 8.6 6.7

The following procedure is followed for homogeneously miscible polymer mixtures: The Hansen solubility parameters of a respective polymer are multiplied in each case by the molar fraction of this polymer in the polymer component and the proportional values are then added in order to arrive at the respective parameter of the polymer component.

For a number of monomers suitable for the polyacrylate of the present invention, the respective Hansen solubility parameters are listed in Table 3 of the Examples, so that the above values for polymer components with polymers formed therefrom are readily ascertainable.

R ¹ in the formula (I) preferably represents a radical selected from the group consisting of methyl, n-butyl and 2-ethylhexyl radicals, more preferably n-butyl and 2-ethylhexyl radicals. Most preferably, R ¹ in the formula (I) is an n-butyl radical.

R ² in the formula (II) is preferably a methoxyethyl radical. Methoxyethyl acrylate is in the monomer composition of the polyacrylate according to the invention preferably up to 65 wt .-%, in particular to 30 to 60 wt .-%, included.

R ³ in the formula (III) is preferably a hydrogen atom.

In one embodiment, the polyacrylate according to the invention is attributable to the following monomer composition: 2-ethylhexyl acrylate up to 60% by weight, acrylic acid up to 10% by weight and methoxyethyl acrylate up to 65% by weight, in particular from 30 to 60% by weight .-%. In a further embodiment, the polyacrylate according to the invention is attributable to the following monomer composition: n-butyl acrylate up to 70% by weight, acrylic acid up to 10% by weight and methoxyethyl acrylate up to 65% by weight, in particular from 30 to 60% wt .-%.

The polyacrylate according to the invention is preferably crosslinked. Particularly preferably, the polyacrylate is thermally crosslinked. Thermal crosslinking can be carried out under much milder conditions than e.g. a radiation-induced cross-linking, which can occasionally also have a destructive effect. However, according to the invention it is also possible to effect crosslinking of the polyacrylate exclusively or additionally by actinic radiation, it being possible to add any necessary or promoting crosslinker substances, e.g. UV-crosslinking agents.

Preferably, the polyacrylate of the invention is thus thermally crosslinked, i. by means of substances which allow (initiate) and / or promote a crosslinking reaction under the influence of thermal energy. Preferred thermal crosslinkers are covalently reacting crosslinkers, in particular epoxides, isocyanates and / or aziridines, and coordinative crosslinkers, particularly preferably metal chelates, in particular aluminum, titanium, zirconium and / or iron chelates. Combinations of various crosslinkers, e.g. a combination of one or more epoxides with one or more metal chelates.

Very particularly preferred metal chelates are aluminum chelates, for example aluminum (III) acetylacetonate. These crosslinkers are preferably used in an amount of 0.01 to 0.1 part by weight, especially preferably from 0.02 to 0.08 parts by weight, in each case based on 100 parts by weight of the polyacrylate (solvent-free) used.

Very particularly preferred thermal crosslinkers are epoxides, especially those having tertiary amine functions such as e.g. Tetraglycidyl meta-xylenediamine (N, N, N ', N'-tetrakis (oxiranylmethyl) -1,3-benzenedimethanamine). These compounds are preferably used in an amount of 0.03 to 0.1 parts by weight, particularly preferably 0.04 to 0.07 parts by weight, in each case based on 100 parts by weight of the polyacrylate (solvent-free) ,

For the preparation of polyacrylates according to the invention, it is possible in principle to use all free-radical or free-radically controlled polymerizations, as well as combinations of different polymerization processes. In addition to conventional, free radical polymerization, these are z. For example, the ATRP, the nitroxide / TEMPO controlled polymerization or the RAFT process.

Another object of the invention is a pressure-sensitive adhesive which contains at least a total of at least 50 wt .-% of at least one inventive polyacrylate. A pressure-sensitive adhesive according to the invention is distinguished by high resistance to chemicals.

Under a pressure-sensitive adhesive or a pressure-sensitive adhesive according to the invention, as is common in common usage, understood a substance which is permanently tacky and tacky at least at room temperature. It is characteristic of a pressure-sensitive adhesive that it can be applied by pressure to a substrate and adhere there, whereby the pressure to be applied and the duration of this pressure are not further defined. In general, but basically depending on the precise nature of the pressure-sensitive adhesive and the substrate, the temperature and the humidity, the application of a short-term, minimal pressure, which does not exceed a slight touch for a short moment to achieve the adhesion effect ranges in In other cases, a longer-term exposure time of higher pressure may be necessary.

Pressure-sensitive adhesives have special, characteristic viscoelastic properties which lead to permanent tackiness and adhesiveness. Characteristic of them is that when they are mechanically deformed, it comes both to viscous flow processes as well as to build elastic restoring forces. Both processes are in a certain ratio with regard to their respective proportions, depending on the exact composition, the structure and the degree of crosslinking of the PSA as well as on the speed and duration of the deformation and on the temperature.

The proportional viscous flow is necessary to achieve adhesion. Only the viscous components, often caused by macromolecules with relatively high mobility, allow good wetting and good flow onto the substrate to be bonded. A high proportion of viscous flow leads to a high pressure tack (also referred to as tack or surface tack) and thus often to a high adhesion. Strongly crosslinked systems, crystalline or glassy solidified polymers are usually not or at least only slightly tacky due to the lack of flowable components.

The proportional elastic restoring forces are necessary to achieve cohesion. They are caused for example by very long-chained and strongly entangled as well as by physically or chemically crosslinked macromolecules and allow the transmission of forces acting on an adhesive bond forces. They result in an adhesive bond being able to withstand a sustained load acting on it, for example in the form of a permanent shearing load, to a sufficient extent over a relatively long period of time.

For a more detailed description and quantification of the amount of elastic and viscous portion and the ratio of the proportions to one another, the variables storage modulus (G ') and loss modulus (G ") which can be determined by means of dynamic mechanical analysis (DMA) are used Proportion, G "is a measure of the viscous component of a substance. Both quantities depend on the deformation frequency and the temperature.

The sizes can be determined with the help of a rheometer. The material to be examined is exposed to a sinusoidal oscillating shear stress in a plate-and-plate arrangement, for example. In shear stress controlled devices, the deformation as a function of time and the time lag of this deformation are compared with the introduction of the shear stress measured. This time offset is referred to as the phase angle δ.

The storage modulus G 'is defined as follows: G' = (τ / γ) • cos (δ) (τ = shear stress, γ = deformation, δ = phase angle = phase shift between shear stress vector and deformation vector). The definition of the loss modulus G "is: G" = (τ / γ) • sin (δ) (τ = shear stress, γ = deformation, δ = phase angle = phase shift between shear stress vector and deformation vector).

A composition is especially considered as a pressure-sensitive adhesive and is in the sense of the invention particularly defined as such, if at 23 ° C in the deformation frequency range of 10 ° to 10 ¹ rad / sec both G 'and G "at least in part in the range of 10 ^third There are up to 10 ⁷ Pa. "part" means that at least a portion of the G 'curve is within the window, the wheel through the deformation of the frequency range including 10 ° up to and including 10 ¹ / sec (abscissa) and the range of the G' Values of 10 ³ up to and including 10 ⁷ Pa (ordinate) are clamped, and if at least a portion of the G "curve is also within the corresponding window.

The polyacrylate according to the invention is preferably tacky. In the simplest case, the pressure-sensitive adhesive of the invention therefore consists of one or more polyacrylates according to the invention. Manufacturing-related impurities such as solvent residues or unreacted monomers are irrelevant here.

In one embodiment, the pressure-sensitive adhesive composition according to the invention comprises at least one tackifier resin, at least one reactive resin and / or at least one plasticizer.

Adhesive resins, also referred to as tackifying resins, are frequently mixed with pressure-sensitive adhesives for fine adjustment of the pressure-sensitive adhesive properties.

According to the invention, "resins" are understood to mean, in particular, those oligomeric and (low) polymeric compounds whose number-average molar mass Mn is not more than 5,000 g / mol. Of course, short-chain polymerization products which are formed during the polymerization of the polyacrylate according to the invention are not subsumed under the term "resins".

Adhesive resins often have softening points in the range of 80 to 150 ° C. The information on the softening point T _E of oligomeric and polymeric compounds, such as the resins, refer to the ring-ball method according to DIN EN 1427: 2007 with appropriate application of the provisions (investigation of Oligomer- or polymer sample instead of bitumen in otherwise maintained procedure). The measurements are carried out in the glycerol bath.

The pressure-sensitive adhesive composition according to the invention preferably contains at least one adhesive resin selected from the group consisting of pinene and indene resins; Rosin and rosin derivatives such as rosin esters, also by z. B. disproportionation or hydrogenation stabilized rosin derivatives; polyterpene; Terpene phenol resins; alkylphenol; and aliphatic, aromatic and aliphatic-aromatic hydrocarbon resins.

Reactive resins are understood as meaning those resins which have functional groups such that they can chemically react with other constituents of the PSA, in particular the polyacrylate or the polyacrylates, with suitable activation.

Adhesive and / or reactive resins are preferably contained in the pressure-sensitive adhesive of the invention to a total of at most 30% by weight. Both one or more tackifier resins and one or more reactive resins and one or more tackifier resins and one or more reactive resins may be present.

The pressure-sensitive adhesive of the invention preferably contains at least one plasticizer selected from the group consisting of (meth) acrylate oligomers, phthalates, hydrocarbon oils, cyclohexanedicarboxylic acid esters, water-soluble plasticizers, soft resins, phosphates and polyphosphates. Plasticizers are preferably contained in the pressure-sensitive adhesive of the invention to a total of at most 30% by weight.

Preferably, the proportion of tackifier resins, reactive resins and plasticizers together at the pressure-sensitive adhesive of the invention is at most 40% by weight.

In order to optimize the properties of the PSA according to the invention, it may also contain other common additives such as fillers, for example electrically conductive fillers, thermally conductive fillers and the like, or flame retardants, for example ammonium polyphosphate and its derivatives.

In one embodiment, the pressure-sensitive adhesive of the invention is foamed. A "foamed pressure-sensitive adhesive" is understood to mean a pressure-sensitive adhesive which comprises an adhesive-tacky matrix material and a plurality of gas-filled cavities, so that the density of this pressure-sensitive adhesive composition is reduced compared to the bare matrix material without cavities. The foaming of the matrix material of the foamed pressure-sensitive adhesive can in principle be effected in any desired manner. For example, the pressure-sensitive adhesive can be foamed by means of an introduced or released in its propellant gas. The foamed pressure-sensitive adhesive preferably contains at least partially expanded hollow microspheres. These are understood to mean at least partially expanded microspheres which are elastic and expandable in their ground state and have a thermoplastic polymer shell. These balls are - in the ground state - filled with low-boiling liquids or liquefied gas. As shell material find in particular polyacrylonitrile, PVDC, PVC or polyacrylates use. Hydrocarbons of the lower alkanes, for example isobutane or isopentane, which are enclosed as liquefied gas under pressure in the polymer shell, are in particular used as the low-boiling liquid. For such microspheres, the term "microballoons" is also common.

By heat on the microballoons softens the outer polymer shell. At the same time, the liquid propellant gas in the casing changes into its gaseous state. The microballoons expand irreversibly and expand in three dimensions. The expansion is completed when the internal and external pressures equalize. As the polymeric shell is preserved, this results in a closed-cell foam.

There are a variety of types of microballoons available commercially, which differ essentially by their size (6 to 45 microns in diameter in the unexpanded state) and their required for expansion starting temperatures (75 to 220 ° C). Unexpanded types of microballoon are also available as aqueous dispersion with a solids or microballoon content of about 40 to 45 wt .-%, also as polymer-bound microballoons (masterbatches), for example, in ethylene vinyl acetate having a microballoon concentration of about 65 wt .-%. Both the microballoon dispersions and the masterbatches, like the unexpanded microballoons, are suitable as such for producing the foamed pressure-sensitive adhesive.

A foamed PSA of the invention can also be produced with so-called pre-expanded hollow microspheres. In this group, the expansion takes place even before the mixing into the polymer matrix.

According to the invention, the foamed PSA preferably contains at least partially expanded hollow microspheres, irrespective of their preparation route and of the starting form of the hollow microspheres used. The term "at least partially expanded hollow microspheres" according to the invention is understood to mean that the hollow microspheres are expanded at least to the extent that a density reduction of the PSA is effected to a technically meaningful extent compared to the same adhesive with the unexpanded hollow microspheres. This means that the microballoons do not necessarily have to be fully expanded. Preferably, the "at least partially expanded hollow microspheres" are each expanded to at least twice their maximum extent in the unexpanded state.

The term "at least partially expanded" refers to the state of expansion of the individual hollow microspheres and is not intended to indicate that only a portion of the microspheres of interest must be expanded. If, therefore, "at least partially expanded hollow microspheres" and unexpanded hollow microspheres are contained in the pressure-sensitive adhesive, then this means that unexpanded (not expanded, ie also not expanded) hollow microspheres do not belong to the "at least partially expanded hollow microspheres".

The preparation of a pressure-sensitive adhesive composition according to the invention is preferably carried out in such a way that the polyacrylate or the polyacrylates are first prepared by free-radical polymerizations from the correspondingly basic monomer mixtures. In the case of several polyacrylates, these are then intimately mixed. If provided, crosslinkers are added during or preferably after the polymerization. If further additives are to be added, these are also added.

A pressure-sensitive adhesive according to the invention is preferably coated on a support or release liner as a solution, if appropriate after setting a certain solids content. The coating is preferably carried out by means of conventional coating methods such as anilox roller coating, comma coating, multi-roll coating or in a printing process. The solvent can then be removed in a drying tunnel or oven.

The crosslinking is carried out when using thermal crosslinkers usually lower proportions at room temperature and larger amounts of heat, especially during removal of the solvent. Coordinative crosslinkers cross-link the polyacrylate, as a rule, independently of temperature; For this reason, substances are added occasionally, which initially block the crosslinker. These are then removed with the solvent, so that at this time immediately uses the crosslinking.

Alternatively, the coating can also be carried out in a solvent-free process. For this purpose, the polyacrylate is heated in an extruder and melted. In the extruder, further process steps such as mixing with additives, filtration or degassing can take place. The melt is then applied by means of a calender on a support or a release liner as a layer.

Another object of the invention is an adhesive tape comprising a pressure-sensitive adhesive according to the invention.

In the simplest case, an adhesive tape according to the invention consists only of a pressure-sensitive adhesive of the invention. In order to be able to apply the adhesive tape wound into a roll of rolls or cross-wound into a bobbin without it sticking to itself, the pressure-sensitive adhesive is preferably covered with at least one release liner.

An adhesive tape according to the invention may comprise, in addition to a pressure-sensitive adhesive composition according to the invention, at least one support and optionally also further layers, for example further pressure-sensitive adhesive layers, barrier layers, further reinforcing support layers, etc. In principle, there are no restrictions with regard to the configuration of the carrier and the further layers. Typical support materials are, for example, fabrics, scrims and plastic films, for example PET films and polyolefin films. Also in such embodiments at least one pressure sensitive adhesive of the adhesive tape is preferably covered with a release liner to allow easy unwinding and to protect the pressure sensitive adhesive (s) from contamination. Release liners usually consist of a single- or double-sided siliconized plastic film (e.g., PET or PP) or a siliconized paper support. They are not attributed to the tape, but are only temporarily connected as an aid with this.

Another object of the invention is the use of a polyacrylate according to the invention or a pressure-sensitive adhesive according to the invention for the production of bonds in electronic, optical or precision mechanical devices.

Electronic, optical and precision mechanical devices within the meaning of the invention are, in particular, such devices as are used in Class 9 of the International Classification of Goods and Services for the Registration of Marks (Nice Classification); 10th edition (NCL (10-2013)); in the case of electronic, optical or precision engineering equipment, and also watches and timepieces in accordance with Class 14 (NCL (10-2013)),
in particular
scientific, nautical, surveying, photographic, cinematographic, optical, weighing, measuring, signaling, checking (supervision), life-saving and teaching apparatus and instruments;
Apparatus and instruments for conducting, switching, transforming, accumulating, regulating and controlling electricity;
Image recording, processing, transmitting and reproducing apparatus, such as televisions and the like;
Acoustic recording, processing, transmission and reproduction apparatus, such as radios and the like;
Computers, computing and data processing equipment, mathematical apparatus and instruments, computer accessories, office equipment - such as printers, fax machines, copiers, typewriters -, data storage devices;
Remote communication and multifunction devices with remote communication function, such as telephones, answering machines;
Chemical and physical measuring apparatus, control apparatus and instruments, such as accumulator chargers, multimeters, lamps, tachometers;
Nautical apparatus and instruments;
Optical apparatus and instruments;
Medical equipment and instruments and athletes;
Watches and chronometers;
Solar cell modules, such as electrochemical dye solar cells, organic solar cells, thin-film cells; and
Fire extinguishers.

The technical development is increasingly focused on such devices that are becoming smaller and lighter, so they can be carried by their owner at any time. This is usually done by implementing small weights and appropriate size of such devices. Such devices are referred to as mobile devices or portable devices. In this development trend, precision mechanical and optical devices are increasingly (also) provided with electronic components, which increases the possibilities of minimization. Due to the entrainment of the mobile devices, these are subjected to increased loads, in particular mechanical and chemical stresses, such as by abutment on edges, by dropping, by contact with other hard objects in the pocket, but also by the permanent movement by being carried along. However, mobile devices are also more exposed to exposure to moisture, temperature, and the like than "immobile" devices that are typically installed indoors and are not or rarely moved. The adhesive used according to the invention has been found to be particularly preferred to withstand such disturbing influences and in the ideal case also to weaken or compensate.

A polyacrylate according to the invention or a pressure-sensitive adhesive of the invention is therefore preferably used for the production of bonds in portable electronic, optical or precision mechanical devices. Such portable devices are in particular:

Cameras, digital cameras, photography accessories (such as light meters, flash units, irises, camera housings, lenses, etc.), movie cameras, video cameras small computers (mobile computers, handheld computers, calculators), laptops, notebooks, netbooks, ultrabooks, tablet computers, handhelds, electronic diaries and organizers (so-called "electronic organizers" or "personal digital assistants", PDAs, palmtops), modems;
Computer accessories and control units for electronic devices such as mice, character pads, graphics tablets, microphones, speakers, game consoles, gamepads, remote controls, remote controls, touch pads;
Monitors, displays, screens, touch screens (touch screens, touch screen devices), beamer;
Electronic book readers ("e-books");
Small TV sets, pocket televisions, movie players, video players Radios (also small and pocket radios), walkmen, discmen, music players for example CD, DVD, Bluray, cassettes, USB, MP3, headphones Cordless phones, mobile phones, smartphones, two-way radios, hands-free kits, pagers ( Pager, beeper);
Mobile defibrillators, blood glucose meters, sphygmomanometers, pedometers, heart rate monitors;
Flashlights, laser pointers;
Mobile detectors, optical magnifying devices, remote viewing devices, night vision devices, GPS devices, navigation devices, portable satellite communications interface devices;
Data storage devices (USB sticks, external hard drives, memory cards); and
Watches, digital watches, pocket watches, chain watches, stop watches.

In particular, a polyacrylate according to the invention or a pressure-sensitive adhesive according to the invention is used for the production of bonds in smartphones (mobile phones), tablets, notebooks, cameras, video cameras, touch-sensitive devices or touchpads.

Examples:

Preparation of polyacrylates

A 300 L reactor conventional for free-radical polymerizations was charged with a total of 100 kg of the monomers indicated in Table 2 in accordance with the composition likewise indicated there and 72.4 kg of gasoline / acetone (70:30). After passing nitrogen gas through with stirring for 45 minutes, the reactor was heated to 58 ° C and 50 g of Vazo® 67 was added. Subsequently, the jacket temperature was heated to 75 ° C and the reaction was carried out constantly at this outside temperature. After 1 h of reaction time, 50 g of Vazo® 67 were added again. After 3 hours, it was diluted with 20 kg of gasoline / acetone (70:30) and after 6 hours with 10.0 kg of gasoline / acetone (70:30). To reduce the residual initiators, 0.15 kg of Perkadox® 16 were added after 5.5 and after 7 hours. The reaction was stopped after a reaction time of 24 hours and cooled to room temperature. The solution was adjusted to a solids content of 38% by weight. Subsequently, 0.075% by weight, based on the polyacrylate, of Erysis GA 240 were stirred in as crosslinking agent.

The resulting composition was coated in solution by means of a comma bar on a siliconized PET film. The solvent was removed in a drying tunnel (20 min, 80 ° C). The polyacrylate thus obtained was applied to a backing (23 .mu.m etched PET film), the application weight was 50 g / cm ² .

Adhesion and chemical resistance test

After peeling off the siliconized PET film, the adhesive tapes as obtained above were applied in a width of 10 mm each onto a previously cleaned ASTM steel plate and rolled back and forth five times in each direction with a 4 kg roller. Subsequently, the bonds thus obtained for 24 h at standard conditions (air, 23 ° C, 50% relative humidity) stored.

The sample samples were then stored for 72 h in a sealed box in a temperature-controlled at 60 ° C water bath, each one sample was immersed in the test chemical and then stored completely surrounded by this and the respective reference sample was stored in air. Test chemical 1: Oleic acid with a purity of> 85% Test chemical 2: Ethanol / water 85/15 (parts by weight).

After the boxes had been removed from the water bath and the sample samples from the boxes, the sample samples were carefully cleaned with a cloth and after 2 h of conditioning in standard climate, the bond strength was determined.

The adhesive strength was determined at a test climate of 23 ° C +/- 1 ° C temperature and 50% +/- 5% relative humidity. The adhesive tape was peeled off the steel substrate at a speed of 300 mm / min and at an angle of 180 °.

The measurement results (Table 2) are given in N / cm and averaged from three measurements.

n-BA

- n-Butylacrylat

EHA

- 2-Ethylhexylacrylat

MA

- Methylacrylat

AS

- Acrylsäure

STA

- Stearylacrylat

IBOA

- Isobornylacrylat

MEA

- Methoxyethylacrylat

Vgl.

- Vergleichsbeispiel

Tabelle 3: Hansen-Löslichkeitsparameter ausgewählter Monomere HSP (Stefanis-Panayiotou) CAS Monomer δ_d δ_p δ_h 79-10-7 Acrylsäure 17,7 8,6 11,1 141-32-2 n-Butylacrylat 17,1 8,6 6,5 689-12-3 Isobutylacrylat 16,9 8,2 6,6 140-88-5 Ethylacrylat 17,1 9,2 7,3 103-11-7 2-Ethyhexylacrylat 16,7 7,0 4,7 2499-95-8 Hexylacrylat 17,0 7,9 5,7 818-61-1 Hydroxyethylacrylat 17,8 12,0 15,3 5888-33-5 Isobornylacrylat 17,6 6,1 4,1 29590-42-9 Isooctylacrylat 16,8 7,0 5,0 96-33-3 Methylacrylat 17,2 9,5 7,7 3121-61-7 Methoxyethylacrylat 17,5 10,7 7,8 925-60-0 Propylacrylat 17,1 8,9 6,9 149021-58-9 Propylheptylacrylat 16,7 6,4 3,9 1663-39-4 tert. -Butylacrylat 16,4 9,5 6,0 The tapes are considered to be resistant to the test chemicals, provided that they still show adhesion after storage. Table 2: Composition of polyacrylates, results No. Composition of the monomer base Hansen parameter δ _p Bond strength reference sample Adhesive strength after storage in oleic acid (N / cm) Adhesive strength after storage in ethanol / water (N / cm) 1 43.5% by weight of n-BA 8.2 7.5 0 0.57 (See.) 43.5% by weight EHA 10% by weight of MA 3% by weight of AS 2 47.5% by weight of n-BA 8.0 8.5 0 0.63 (See.) 47.5% by weight EHA 5% by weight of AS 3 76% by weight EHA 6.6 4.8 0 0.43 (See.) 20% by weight STA 4% by weight of AS 4 29% by weight of n-BA 7.9 15.13 0 0.56 (See.) 59% by weight EHA 12% by weight of AS 5 68% by weight EHA 6.8 7.9 0 0.74 (See.) 30% by weight of IBOA 2% by weight of AS 6 97% by weight MEA 10.6 10.9 5.9 0 (See.) 3% by weight of AS 7 40% by weight EHA 9.4 5.1 0.69 0.87 57% by weight MEA 3% by weight of AS 8th 50% by weight EHA 9.1 9.53 1 0.68 47% by weight MEA 3% by weight of AS 9 60% by weight of n-BA 9.3 12.6 2 0.5 37% by weight MEA 3% by weight of AS

n-BA

- n-butyl acrylate

EHA

2-ethylhexyl acrylate

MA

- Methyl acrylate

AS

- acrylic acid

STA

- stearyl acrylate

IBOA

- Isobornyl acrylate

MEA

- Methoxyethyl acrylate

See.

- Comparative Example

Table 3: Hansen solubility parameters of selected monomers HSP (Stefanis-Panayiotou) CAS monomer δ _d δ _p δ _h 79-10-7 acrylic acid 17.7 8.6 11.1 141-32-2 n-butyl acrylate 17.1 8.6 6.5 689-12-3 isobutyl 16.9 8.2 6.6 140-88-5 ethyl acrylate 17.1 9.2 7.3 103-11-7 2-Ethyhexylacrylat 16.7 7.0 4.7 2499-95-8 hexyl acrylate 17.0 7.9 5.7 818-61-1 hydroxyethyl 17.8 12.0 15.3 5888-33-5 isobornyl 17.6 6.1 4.1 29590-42-9 isooctyl 16.8 7.0 5.0 96-33-3 methyl acrylate 17.2 9.5 7.7 3121-61-7 methoxyethyl 17.5 10.7 7.8 925-60-0 propyl 17.1 8.9 6.9 149021-58-9 propylheptyl 16.7 6.4 3.9 1663-39-4 tert. butyl acrylate 16.4 9.5 6.0

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited patent literature

• WO 2016/089687 A1 [0004]
• WO 2017/132058 A1 [0005]
• DE 102015215247 A1 [0006]
• US 5665835 [0007]

Cited non-patent literature

• Hansen Solubility Parameters: A User's Handbook, Second Edition; Charles M. Hansen; 2007 CRC Press; ISBN 9780849372483 [0012]
• Prediction of Hansen Solubility Parameters with a New Group Contribution Method; Int. J. Thermophys. (2008) 29: 568-585 [0014]
• Int. J. Thermophys. (2008), Tables 3 to 6, pages 578 to 582 [0015]

Claims (9)

Polyacrylate, characterized in that the polyacrylate is attributable to the following monomer composition: a) from 25 to 70% by weight of at least one acrylic acid ester of the formula (I) CH ₂ = CH-C (O) OR ¹ (I), wherein R ^{1 is} a linear or branched alkyl group having 1 to 10 C atoms; b) from 25 to 70% by weight of at least one acrylic acid ester of the formula (II) CH ₂ = CH-C (O) OR ² (II), wherein R ^{2 is} an alkoxyalkyl radical having 2 to 5 C atoms; c) 0.5 to 10% by weight of at least one acrylate monomer of the formula (III) CH ₂ = CH-C (O) OR ³ (III), wherein R ^{3 is} an H atom or a hydroxyalkyl radical having 1 to 4 carbon atoms. Polyacrylate according to Claim 1 characterized in that the polyacrylate has a Hansen solubility parameter of polar interactions of 8.5 to 9.5. Polyacrylate according to one of Claims 1 and 2 , characterized in that R ^{1 is} a radical selected from the group consisting of methyl, n-butyl and 2-ethylhexyl radicals. Polyacrylate according to one of the preceding claims, characterized in that R ^{2 is} a methoxyethyl radical. Polyacrylate according to one of the preceding claims, characterized in that R ^{3 represents} a hydrogen atom. Pressure-sensitive adhesive composition comprising at least 50% by weight of at least one polyacrylate according to one of Claims 1 to 5 , Pressure-sensitive adhesive according to Claim 6 , characterized in that the pressure-sensitive adhesive composition contains an adhesive resin and / or a plasticizer. Adhesive tape comprising a pressure-sensitive adhesive according to one of Claims 6 and 7 , Use of a pressure-sensitive adhesive according to one of Claims 6 and 7 for the production of gluing in electronic, optical or precision mechanical devices.