JP2015127141A - Carbon fiber composite laminate - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a carbon fiber composite laminate having an excellent balance between low expansivity, good surface appearance, and press formability.SOLUTION: There is provided a carbon fiber composite laminate having at least a structure of three layers, comprising thermoplastic resin layers (A layers) containing 30 pts.mass or more and 200 pts.mass or less of a tabular inorganic filler having an aspect ratio of 20 or more and 500 or less relative to 100 pts.mass of a thermoplastic resin and a carbon fiber layer (B layer). The A layers form the front and back layers. A carbon fiber bundle in the B layer has a maximum diameter of 10 μm or more and 1000 μm or less, and the carbon fiber has a mean fiber length of 0.1 mm or more and less than 5 mm.

Description

  The present invention relates to a laminate in which a thermoplastic resin and carbon fiber are combined.

  In recent years, there is a growing need for molded products that are lightweight, high-strength, and excellent in heat resistance, such as housings for large electrical appliances, interior materials and exterior materials for automobiles and railways. In particular, such a molded article is required to have a low responsiveness to dimensional change with respect to heat, that is, a low linear expansion material. Based on such a background, a low linear expansion material in which a thermoplastic resin and inorganic fibers are combined has been proposed.

  For example, Patent Document 1 (Japanese Patent Laid-Open No. 2010-254276) discloses a laminate for an automobile exterior having a carbon fiber reinforced layer containing carbon fibers and a thermoplastic resin layer and having a specific linear expansion coefficient. And discloses that the thermoplastic resin layer is a polyolefin-based resin, and various inorganic fillers that are fillers may be included as additives.

  Patent Document 2 (Japanese Patent Application Laid-Open No. 2008-45040) discloses that the main layer includes a thermoplastic resin (A) and a filler (B) composed of glass fiber and at least one filler other than glass fiber. Thus, there is disclosed a single-layer or multi-layer low-linear expansion extruded sheet in which the main layer contains the filler (B) in a specific ratio and has a specific linear expansion coefficient and Charpy impact strength.

  Patent Document 3 (Japanese Patent Application Laid-Open No. 2007-169561) discloses (A) polypropylene resin, (B) elastomer, (C) talc, and (D) fine carbon fibers having a fiber diameter of 100 nm or less. A molded body is disclosed, which is characterized in that the average fiber length of the component (D) in the molded body is 2.5 μm or more.

JP 2010-254276 A JP 2008-45040 A JP 2007-169561 A

  In the laminate disclosed in Patent Document 1, an attempt is made to express low linear expansion with a single carbon fiber reinforced layer, and a known filler or reinforcing fiber is further contained to improve the overall warpage. It is said that a thermoplastic resin layer may be provided. However, in this configuration, the formability (press formability) when the laminate is subjected to secondary processing by thermoforming or vacuum forming is not sufficient, and it is not sufficient from the viewpoint of reducing the weight of the laminate itself. Further, no consideration is given to the appearance failure due to the unevenness of the surface of the laminate depending on the carbon fiber used, and there is room for improvement in the appearance of the laminate.

  Since the sheet disclosed in Patent Document 2 contains a considerable amount of glass fiber and filler in the main layer, it has low linear expansion, but press formability during secondary processing, particularly drawing die The following ability is not sufficient, and both formability and low linear expansion are not achieved.

  The molded body disclosed in Patent Document 3 is excellent in press formability at the time of secondary processing, but low linear expansion is not sufficient because carbon fiber is too fine, and formability and low linear expansion Are not compatible.

  That is, in the prior art, it has not been possible to obtain a laminate that balances low linear expansion, good surface appearance, and the ability to follow a drawing die during press molding.

  An object of the present invention is to solve the above-mentioned conventional problems and to provide a carbon fiber composite laminate excellent in the balance between low linear expansion, good surface appearance and press formability.

  As a result of intensive studies in view of the above problems, the present inventors have found that a specific carbon fiber composite laminate is excellent in balance between low linear expansion, good surface appearance and press formability, and completed the present invention. It came to do.

That is, the present invention is as follows.
[1] A carbon fiber composite laminate having at least a three-layer structure, wherein 30 to 200 parts by mass of plate-like inorganic particles having an aspect ratio of 20 to 500 with respect to 100 parts by mass of the thermoplastic resin. It has a thermoplastic resin layer (A layer) and a carbon fiber layer (B layer), the A layer is a front and back layer, and the maximum diameter of the carbon fiber bundle in the B layer is 10 μm or more and 1000 μm or less. And an average fiber length of the carbon fibers is 0.1 mm or more and less than 5 mm.
[2] The carbon according to [1], wherein the thermoplastic resin used in the A layer is at least one resin selected from the group consisting of a polyolefin resin, a polycarbonate resin, a polyamide resin, and a polyester resin. Fiber composite laminate.
[3] The carbon fiber composite laminate according to [1] or [2], wherein the B layer is a layer formed using carbon fiber mat or carbon fiber paper as a carbon fiber material.
[4] The carbon fiber composite laminate according to any one of [1] to [3], wherein the maximum cross-sectional height (Rt) of the surface of the A layer is 3 μm or less.

  According to the present invention, a carbon fiber composite having an excellent balance of low linear expansion, good surface appearance and press formability, and suitable for a casing of a large electrical appliance, an interior material of an automobile or a railway, an exterior material, etc. A laminate can be provided.

[Thermoplastic resin layer (A layer)]
The thermoplastic resin layer (A layer) constituting the carbon fiber composite laminate of the present invention (hereinafter referred to as “the present laminate”) is a plate having an aspect ratio of 20 or more and 500 or less with respect to 100 parts by mass of the thermoplastic resin. It is a layer containing 30 parts by mass or more and 200 parts by mass or less of inorganic particles, and exists as a front and back layer of the laminate.

[Thermoplastic resin]
The thermoplastic resin that can be used for the A layer is preferably at least one resin selected from the group consisting of polyolefin resins, polycarbonate resins, polyamide resins, and polyester resins. These resins may be used alone or in combination of two or more.
For example, by using a polyolefin-based resin, the laminate is excellent in moldability and particularly in impact resistance. Moreover, by using a polycarbonate resin, a polyamide resin, or a polyester resin, the laminate is excellent in moldability and particularly in heat resistance.

<Polyolefin resin>
The polyolefin resin that can be used for the A layer is not particularly limited, and is a homopolymer obtained by polymerizing an α-olefin such as ethylene, propylene, 1-butene, 4-methyl-1-pentene, 1-hexene. Or a copolymer is mentioned. Also, two or more of these homopolymers or copolymers can be mixed. Among these, it is preferable to use a polypropylene resin or a polyethylene resin, and it is particularly preferable to use a polypropylene resin from the viewpoint of lightness.

(Polypropylene resin)
The polypropylene-based resin used for the A layer is a resin in which propylene exceeds 50 mol%, preferably 70 mol% or more, more preferably 90 mol% or more, among the constituent monomers. Propylene homopolymer), or one of α-olefins such as propylene and ethylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene or the like Examples thereof include random copolymers and block copolymers with two or more kinds. Among these, homopolypropylene is more preferably used from the viewpoint of rigidity and heat resistance.

  In addition, the polypropylene resin may be one in which a part of its molecular structure is modified with acid or alkali. Specific examples include maleic acid-modified polypropylene resins and amine-modified polypropylene resins.

Moreover, as a polypropylene resin, it is preferable that the isotactic pentad fraction (mmmm fraction) which shows stereoregularity is 80 to 99%. The isotactic pentad fraction of the polypropylene resin is more preferably 83 to 98%, and still more preferably 85 to 97%. If the isotactic pentad fraction is within such a range, there is little possibility that the strength of the laminate is lowered. The upper limit of the isotactic pentad fraction is defined by the upper limit that can be obtained industrially at the present time, but this is not the case when a more regular resin is developed in the industrial level in the future. is not.
The isotactic pentad fraction (mmmm fraction) is the same direction for all five methyl groups that are side chains with respect to the main chain of carbon-carbon bonds composed of arbitrary five consecutive propylene units. Means the three-dimensional structure located at or its proportion. Signal assignment of the methyl group region is as follows. It conforms to Zambelli et al (Macromolecules 8,687, (1975)).

The melt mass flow rate R _A of the polypropylene resin used for the A layer is measured in accordance with JIS K7210 (1999) under conditions of a temperature of 230 ° C. and a load of 2.16 kgf, and is 0.1 g / 10 min or more and 60 g / 10 min or less. It is preferably 0.1 g / 10 min or more and 30 g / 10 min or less, more preferably 0.1 g / 10 min or more and 20 g / 10 min or less. When R _A is 0.1 g / 10 min or more, followability to the mold during press molding of the laminate is facilitated. On the other hand, when it is 60 g / 10 min or less, there is no fear of flowing out of the mold due to pressurization during press molding of the laminate, and resin impregnation between carbon fibers and fillers becomes easy.

  Mw / Mn, which is a parameter indicating the molecular weight distribution of the polypropylene resin used for the A layer, is measured by a GPC (gel permeation chromatography) method according to JIS K7252-1 (2008), and is 1.5 or more, 10 Or less, more preferably 1.5 or more and 8 or less, and particularly preferably 1.5 or more and 6 or less. The smaller the Mw / Mn, the narrower the molecular weight distribution. When the Mw / Mn is 1.5 or more, the followability to the mold during press molding of the laminate is facilitated. On the other hand, when Mw / Mn is 10 or less, various mechanical properties of the laminate can be satisfied.

  The production method of the polypropylene resin used for the A layer is not particularly limited, and a known polymerization method using a known olefin polymerization catalyst, for example, a multisite catalyst represented by a Ziegler-Natta type catalyst or a metallocene system. Examples thereof include a slurry polymerization method, a melt polymerization method, a bulk polymerization method, a gas phase polymerization method using a single site catalyst represented by a catalyst, and a bulk polymerization method using a radical initiator.

(Polyethylene resin)
The polyethylene-based resin used for the layer A is a resin in which ethylene is more than 50 mol%, preferably 70 mol% or more, more preferably 90 mol% or more among the constituent monomers. , Linear low density polyethylene, linear ultra-low density polyethylene, medium density polyethylene, high density polyethylene, and copolymers based on ethylene, ie, ethylene, propylene, butene-1, pentene-1, hexene 1, α-olefins such as heptene-1 and octene-1; vinyl esters such as vinyl acetate and vinyl propionate; unsaturated carboxylic acid esters such as methyl acrylate, ethyl acrylate, methyl methacrylate, and ethyl methacrylate; conjugates One or two selected from unsaturated compounds such as dienes and non-conjugated dienes It includes copolymers or multicomponent copolymer or a mixture composition with more comonomers.

  Among these polyethylene resins, at least one polyethylene resin selected from low-density polyethylene, linear low-density polyethylene, and high-density polyethylene is preferable, and high in terms of improving the strength and heat resistance of the laminate. More preferred is density polyethylene.

The melt mass flow rate _RA of the polyethylene resin used for the A layer is measured in accordance with JIS K7210 (1999) under conditions of a temperature of 190 ° C. and a load of 2.16 kgf, and is 0.05 g / 10 min or more and 30 g / 10 min or less. It is preferably 0.1 g / 10 min or more and 20 g / 10 min or less, more preferably 1 g / 10 min or more and 20 g / 10 min or less. When _RA is 0.05 g / 10 min or more, followability to the mold during press molding of the laminate is facilitated. On the other hand, when it is 30 g / 10 min or less, there is no risk of flowing out of the mold due to pressurization during press molding of the laminate, and resin impregnation between carbon fibers and fillers is facilitated.

The density of the polyethylene resin used for the A layer can be measured using a density gradient tube method according to JIS K7112 (1999), and is preferably 0.910 to 0.970 g / cm ^3. more preferably .930~0.970g / cm ^3, further preferably 0.940 to 0.970 g / cm ^3. If the density is 0.910 g / cm ³ or more, the laminate satisfies various mechanical properties. On the other hand, if it is 0.970 g / cm < ³ > or less, this laminated body can maintain a lightweight property.

  The production method of the polyethylene resin used for the A layer is not particularly limited, and a known polymerization method using a known olefin polymerization catalyst, for example, a multisite catalyst or a metallocene catalyst represented by a Ziegler-Natta type catalyst. And a polymerization method using a single site catalyst represented by. As a polymerization method of the polyethylene resin, there are a one-stage polymerization, a two-stage polymerization, or a multistage polymerization more than that, and any of these methods can be used.

<Polycarbonate resin>
The polycarbonate resin used for the A layer may be either a homopolymer or a copolymer. Further, the polycarbonate-based resin may have a branched structure, a linear structure, or a mixture of a branched structure and a linear structure. A plurality of polycarbonate resins may be mixed and used.
The so-called polyester carbonate resin (resin having both ester bond and carbonate bond in the molecular chain) is also included in the polycarbonate resin.

Representative examples of the dihydric alcohol (diol) constituting the polycarbonate resin used in the A layer include bisphenols. In particular, 2,2-bis (4-hydroxyphenyl) propane, that is, bisphenol A is preferably used.
In addition, a diol other than bisphenol A may be used alone, or a polycarbonate resin using a plurality of diols may be used, and any of an aromatic diol, an aliphatic diol, and an alicyclic diol may be used.

The melt mass flow rate _RA of the polycarbonate-based resin used for the A layer is measured under conditions of a temperature of 300 ° C. and a load of 1.2 kgf according to JIS K7210 (1999), and is 1 g / 10 min or more and 40 g / 10 min or less. It is preferably 2 g / 10 min or more and 35 g / 10 min or less, more preferably 3 g / 10 min or more and 30 g / 10 min or less. When _RA is 1 g / 10 min or more, followability to the mold during press molding of the laminate is facilitated. On the other hand, when it is 40 g / 10 min or less, there is no fear of flowing out of the mold due to pressurization during press molding of the laminate, and resin impregnation between carbon fibers and fillers is facilitated.

  The production method of the polycarbonate resin used for the A layer is not particularly limited, and examples thereof include a known polymerization method such as a phosgene method, a transesterification method, and a pyridine method.

<Polyamide resin>
The polyamide-based resin used for the A layer is preferably an aliphatic polyamide, obtained by ring-opening homopolymerization of ω-amino acids, obtained by ring-opening copolymerization of different ω-amino acids, or by copolymerization of diamine and dicarboxylic acid. Any of those obtained may be used. An aromatic polyamide or an aromatic-aliphatic polyamide can also be used.

In the case of aliphatic polyamide, the melt mass flow rate _RA of the polyamide-based resin used for the A layer is measured under the conditions of a temperature of 230 ° C. and a load of 2.16 kgf in accordance with JIS K7210 (1999), 0.1 g / 10 min or more, It is preferably 60 g / 10 min or less, more preferably 0.5 g / 10 min or more and 30 g / 10 min or less, and particularly preferably 1 g / 10 min or more and 20 g / 10 min or less. When R _A is 0.1 g / 10 min or more, followability to the mold during press molding of the laminate is facilitated. On the other hand, when it is 60 g / 10 min or less, there is no fear of flowing out of the mold due to pressurization during press molding of the laminate, and resin impregnation between carbon fibers and fillers becomes easy.

  The manufacturing method of the polyamide-type resin used for A layer is not specifically limited, A well-known polymerization method is employable.

<Polyester resin>
The polyester-based resin that can be used for the A layer is preferably an aromatic polyester-based resin from the viewpoint of heat resistance and moldability, and specifically, polyethylene terephthalate, polyethylene naphthalate, polybutylene terephthalate, polytrimethylene terephthalate, and the like. Can be mentioned.

The melt mass flow rate _RA of the polyester-based resin used for the A layer is measured under conditions of a temperature of 230 ° C. and a load of 2.16 kgf in accordance with JIS K7210 (1999), and is 0.1 g / 10 min or more and 60 g / 10 min or less. It is preferably 0.5 g / 10 min or more and 30 g / 10 min or less, more preferably 1 g / 10 min or more and 20 g / 10 min or less. When R _A is 0.1 g / 10 min or more, followability to the mold during press molding of the laminate is facilitated. On the other hand, when it is 60 g / 10 min or less, there is no fear of flowing out of the mold due to pressurization during press molding of the laminate, and resin impregnation between carbon fibers and fillers becomes easy.

  The manufacturing method of the polyester-type resin used for A layer is not specifically limited, A well-known polymerization method is employable.

[Plate-like inorganic particles]
The layer A of the laminate contains 30 to 200 parts by mass of plate-like inorganic particles having an aspect ratio of 20 to 500 with respect to 100 parts by mass of the thermoplastic resin.
The content ratio of the plate-like inorganic particles is preferably 30 parts by mass or more and 160 parts by mass or less, and particularly preferably 30 parts by mass or more and 120 parts by mass or less with respect to 100 parts by mass of the polyolefin resin.
By containing 30 parts by mass or more of the plate-like inorganic particles with respect to 100 parts by mass of the polyolefin-based resin, this laminate contributes to the improvement of low linear expansion. Moreover, it contributes to the improvement of the moldability of this laminated body by containing 200 mass parts or less of plate-shaped inorganic particles with respect to 100 mass parts of polyolefin resin.

Specific examples of the plate-like inorganic particles used for the A layer include metal carbonates such as calcium carbonate, magnesium carbonate, and barium carbonate, metal sulfates such as calcium sulfate, barium sulfate, and magnesium sulfate, calcium oxide, and oxidation. Examples thereof include metal oxides such as magnesium, zinc oxide, alumina, silica, and titanium oxide, metal chlorides such as sodium chloride, magnesium chloride, silver chloride, and calcium chloride, and clay minerals such as talc, clay, mica, and montmorillonite.
Among these, talc or mica is preferably used from the viewpoint of low linear expansion and cost, and mica is particularly preferable.

The average particle size of the plate-like inorganic particles used for the A layer is preferably 1 μm or more and 500 μm or less, more preferably 5 μm or more and 300 μm or less, and particularly preferably 5 μm or more and 100 μm or less.
When the average particle size of the plate-like inorganic particles is 1 μm or more, this laminate contributes to the improvement of low linear expansion. Moreover, if an average particle diameter is 500 micrometers or less, it will contribute to the improvement of the surface external appearance of this laminated body.
In the present invention, the “average particle diameter of the plate-like inorganic particles” means, for example, the short diameter and long diameter of a two-dimensional projection image when the inorganic particles are projected from a certain direction using an image analyzer. After calculating the averaged values for projection images from ten different directions, the maximum value and the minimum value can be calculated as a further averaged value.

The aspect ratio (major axis / minor axis value) of the plate-like inorganic particles used for the A layer is 20 or more and 500 or less, preferably 20 or more and 300 or less, and particularly preferably 20 or more and 100 or less. .
When the aspect ratio of the plate-like inorganic particles is 20 or more, the laminate is excellent in low linear expansion. On the other hand, if the aspect ratio of the plate-like inorganic particles is 500 or less, the laminate is excellent in surface appearance.
The aspect ratio of the plate-like inorganic particles is, for example, the ratio of the minor axis to the major axis (major axis / minor axis) of the two-dimensional projection image when the inorganic particles are projected from a certain direction using an image analyzer. It is possible to calculate and average the projection images from 10 different directions.

  The plate-like inorganic particles used in the A layer may be surface-treated. The surface treatment method is not particularly limited, and examples thereof include a method using a surface treatment agent such as a general silane coupling agent. By surface-treating the plate-like inorganic particles, the effects of improving the dispersibility of the plate-like inorganic particles in the thermoplastic resin and preventing the plate-like inorganic particles from falling off from the A layer can be obtained.

  These plate-like inorganic particles may be used alone or in combination of two or more kinds having different materials, particle sizes and aspect ratios, presence / absence of surface treatment, type of surface treatment agent, and the like.

[Other ingredients]
When the laminate is required to have flame retardancy, the layer A can further contain a flame retardant. The flame retardant used in the A layer is not particularly limited, such as phosphorus flame retardants such as various condensed phosphate esters, nitrogen flame retardants such as melamine, phosphorus / nitrogen flame retardants such as phosphazene, brominated aromatic compounds, etc. One or more known flame retardants such as bromine flame retardants and antimony flame retardants such as antimony trioxide can be appropriately selected and used.

When the flame retardant is contained in the A layer, the content is preferably 20 parts by mass or more and 60 parts by mass or less, and 25 parts by mass or more and 60 parts by mass or less with respect to 100 parts by mass of the thermoplastic resin. Is more preferably 30 parts by mass or more and 60 parts by mass or less.
By containing 20 parts by mass or more of the flame retardant with respect to 100 parts by mass of the thermoplastic resin, the laminate can exhibit excellent flame retardancy. On the other hand, by including 60 parts by mass or less of the flame retardant with respect to 100 parts by mass of the thermoplastic resin, the laminate satisfies various mechanical properties.

  In addition to the components described above, the A layer may appropriately contain other thermoplastic resins and additives generally blended into the resin composition within a range not impairing the characteristics and effects of the present invention. Specific examples of additives include pigments such as carbon black, weather resistance stabilizers, heat resistance stabilizers, antistatic agents, melt viscosity improvers, crosslinking agents, lubricants, nucleating agents, plasticizers, antiaging agents, and antioxidants. , Light stabilizers, ultraviolet absorbers, neutralizers, antifogging agents, antiblocking agents, slip agents or coloring agents.

[Method for producing layer A]
As will be described later, the laminate is obtained by preparing and laminating a thermoplastic resin sheet constituting the A layer and a carbon fiber material constituting the B layer.
It does not specifically limit as a preparation method of the thermoplastic resin sheet which comprises A layer, A well-known melt film-forming method, such as a T die-cast method, a calendar method, a press method, is employable.

  More specifically, the thermoplastic resin, the plate-like inorganic particles, and other components including a flame retardant as required, a method of directly mixing and melt-forming, the thermoplastic resin, Examples include a method of melt-kneading the plate-like inorganic particles and other components including a flame retardant as necessary to prepare a pellet of a mixture and melt-forming a thermoplastic resin sheet using the mixture. Can do.

[Thickness of layer A]
The thickness of the thermoplastic resin sheet constituting the A layer before producing the laminate is not particularly limited, but is preferably 0.5 mm or more and 2.5 mm or less, and is 0.5 mm or more and 2 mm or less. Is more preferably 0.5 mm or more and 1.5 mm or less, and particularly preferably 0.5 mm or more and 1 mm or less. When the thickness of the thermoplastic resin sheet constituting the A layer is 0.5 mm or more, deterioration of the surface appearance such as the exposure of the carbon fiber layer of the B layer on the product surface after press molding can be suppressed. Moreover, if the thickness of the thermoplastic resin sheet which comprises A layer is 2.5 mm or less, lightness can be maintained.

  Further, the thickness of the A layer in the laminate is not particularly limited, but is preferably 0.5 mm or more and 2.5 mm or less, more preferably 0.5 mm or more and 2 mm or less, 0.5 mm or more, More preferably, it is 1.5 mm or less, and particularly preferably 0.5 mm or more and 1 mm or less.

[Carbon fiber layer (B layer)]
The carbon fiber layer (B layer) constituting the laminate is a layer mainly composed of a carbon fiber material. By having a carbon fiber layer, it is possible to achieve excellent low linear expansion for the laminate.

  As a kind of carbon fiber used for B layer, any of pitch type carbon fiber and PAN type carbon fiber may be used, and these may be used in combination, but pitch type carbon fiber is preferred from the viewpoint of low linear expansion. The pitch-based carbon fiber may be either a mesophase pitch-based carbon fiber or an isotropic pitch-based carbon fiber. From the viewpoint of improving the strength and low linear expansion of the laminate, the mesophase pitch-based carbon fiber is used. Is more preferable.

  As the carbon fiber material used for the B layer, a carbon fiber mat or carbon fiber paper is preferable. Both “carbon fiber mat” and “carbon fiber paper” are materials in which carbon fiber bundles are opened and dispersed, and formed and paper-formed by a wet method or a dry method to form a flat film.

  Any carbon fiber material described above preferably contains a binder resin so that the carbon fibers do not easily dissociate, and may be a so-called prepreg in which carbon fiber is impregnated with a binder resin. In general, “carbon fiber mat” is distinguished from “carbon fiber paper” in terms of the content and thickness of the binder resin. Usually, the carbon fiber mat has a larger binder resin content and a larger thickness than the carbon fiber paper.

  The binder resin is not particularly limited, and examples thereof include crystalline thermoplastic resins such as polyolefin resins, polyester resins, polyacetal resins, polyphenylene sulfide resins, and crystalline polyamide resins; aromatic vinyl compound resins (polystyrene elastomers). ), Polycarbonate resins, polyphenylene ether resins, polysulfone resins, polyolefin elastomers, amorphous polyamide resins, and other amorphous thermoplastic resins; unsaturated polyester resins, vinyl ester resins, and other polyester resins; epoxy resins, phenols (resol type) Examples thereof include thermosetting resins such as resins, urea resins, melamine resins, polyimide resins, bismaleimide resins, and cyanate ester resins. Moreover, these copolymers, modified bodies, etc. may be sufficient and these may be used in combination of 2 or more types.

The content when the binder resin is contained in the carbon fiber material is preferably 1 part by mass or more and 90 parts by mass or less, and preferably 5 parts by mass or more and 80 parts by mass or less with respect to 100 parts by mass of the carbon fiber. More preferably, it is more preferably 10 parts by mass or more and 70 parts by mass or less.
By containing a binder resin in such a range, the carbon fiber can be stably formed into a carbon fiber material such as a carbon fiber mat or carbon fiber paper.

Above all, as the carbon fiber material used for the laminate, from the viewpoint of resin impregnation property, low linear expansion property, and cost, the fiber opening can be promoted at the time of paper making, and the carbon fiber paper capable of maintaining a high carbon fiber amount. Is particularly preferred.
The carbon fiber paper is usually produced by either a dry papermaking method or a wet papermaking method, but it is preferable to use one produced by a wet papermaking method from the viewpoint of better fiber opening.
Further, from the viewpoint of low linear expansion, the carbon fiber paper preferably has a large basis weight (carbon fiber amount), but preferably 20 to 100 g / m in view of the balance between the productivity of the paper itself and the cost. ² , more preferably 30 to 100 g / m ² , and particularly preferably 40 to 100 g / m ² basis weight.

In this laminated body, the maximum diameter of the carbon fiber bundle in the B layer is 10 μm or more and 1000 μm or less. The maximum diameter of the carbon fiber bundle in the B layer is more preferably 10 μm or more and 950 μm or less, and particularly preferably 10 μm or more and 900 μm or less.
Normally, the average fiber diameter of one carbon fiber is 7 to 10 μm, but these are aggregated by electrostatic adhesion or a converging agent to form a carbon fiber bundle. For such a carbon fiber bundle, the balance between the low linear expansion property, good surface appearance and press formability of the laminate is maintained by controlling the maximum diameter of the laminate to 10 μm or more and 1000 μm or less. Can do.
The maximum diameter of the carbon fiber bundle can be measured and evaluated by the method described in the examples described later.

Moreover, in this laminated body, the average fiber length of the carbon fiber in B layer is 0.1 mm or more and less than 5 mm. The average fiber length of the carbon fibers in the B layer is more preferably 0.1 mm or more and 4.5 mm or less, and particularly preferably 0.1 mm or more and 4.0 mm or less.
By controlling the average fiber length of the carbon fibers to be 0.1 mm or more and less than 5 mm, the balance between the low linear expansion property, good surface appearance and press formability of the laminate can be maintained.
In addition, the average fiber length of carbon fiber can be measured and evaluated by the method as described in the Example mentioned later.

  As a preferable method for setting the maximum diameter of carbon fiber bundles in B layer and the average fiber length of carbon fibers in the above-mentioned range in the present laminate, for example, a method of sufficiently opening the fibers when producing the carbon fiber material. Is mentioned. Specifically, when carbon fiber paper is produced by a wet papermaking method, a method of controlling the number of revolutions of a disaggregator used for fiber opening is exemplified. In the case of producing by a dry papermaking method, or for carbon fiber materials other than carbon fiber paper, the fiber opening may be performed by controlling the fiber opening conditions.

  The maximum diameter of the carbon fiber bundle and the average fiber length of the carbon fiber are contradictory characteristics.If the fiber is excessively opened, the maximum diameter of the carbon fiber bundle becomes small, but the average fiber length becomes too short, resulting in low linear expansion. Not fully expressed. On the other hand, if the fiber opening is insufficient, the maximum diameter of the carbon fiber bundle becomes large, and the laminate may have a poor appearance or the press formability may be insufficient. By controlling the maximum diameter of the carbon fiber bundle and the average fiber length of the carbon fibers in the above range, the present laminate can maintain a balance between low linear expansion, good surface appearance and press formability.

  The preferable range of the maximum diameter of the carbon fiber bundle and the average fiber length of the carbon fiber in the carbon fiber material used for the B layer is the same as the range of the maximum diameter of the carbon fiber bundle and the average fiber length of the carbon fiber in the B layer. It is.

The thickness of the B layer in the present laminate is not particularly limited, but is preferably 0.1 mm or more and 0.3 mm or less, more preferably 0.1 mm or more and 0.25 mm or less, 0.1 mm or more, It is especially preferable that it is 0.2 mm or less.
If the thickness of the B layer is 0.1 mm or more, the laminate can exhibit excellent low linear expansion. Moreover, if the thickness of B layer is 0.3 mm or less, there are few surface unevenness | corrugations of this laminated body, and it is excellent in surface appearance.
The carbon fiber material used for the B layer has a variety of thicknesses because the porosity varies depending on the type. Therefore, the carbon fiber material having such a thickness that the preferable thickness when provided in the laminate is within the above range is preferable.

[Other layers]
In addition to the A layer and the B layer, the present laminate may be provided with other layers as long as the features and effects of the present invention are not impaired.
Specifically, in this laminate, the A layer is a front and back layer, and for example, it may have a configuration of A layer / B layer / A layer, but between the A layer and the B layer, an adhesive layer as necessary Etc. can also be provided. Furthermore, it can also be set as the laminated body which provided two B layers and provided the other layer between the layers like A layer / B layer / other layer / B layer / A layer.
Moreover, although this laminated body uses A layer as a front and back layer, it does not prevent providing surface protection layers, such as a layer which has designability, such as a printing layer, and an antifouling layer, in the further outside of A layer.

[Method for producing the present laminate]
As described above, the present laminate is obtained by producing and laminating the thermoplastic resin sheet constituting the A layer and the carbon fiber material constituting the B layer, respectively.

More specifically, for example, a step of producing a thermoplastic resin sheet used for the A layer, a step of producing a carbon fiber material used for the B layer by opening a carbon fiber bundle, and the thermoplastic resin sheet and A manufacturing method comprising a step of laminating the carbon fiber material so as to have a configuration of A layer / B layer / A layer, and press molding at an appropriate temperature and pressure condition according to the thermoplastic resin used for the A layer Thus, the present laminate can be obtained.
The manufacturing method described above may be a so-called batch method. While producing the thermoplastic resin sheet used for the A layer, the carbon fiber material used for the B layer is supplied, and press forming while continuously laminating them. The continuous press method may be used.

For example, when the thermoplastic resin used for the A layer is a polyolefin resin, the press molding temperature is preferably 180 to 230 ° C, more preferably 180 to 220 ° C, and particularly preferably 190 to 210 ° C. . Further, the pressing pressure is preferably 0.5 to 4.0 MPa, more preferably 0.5 to 3.0 MPa, and particularly preferably 1 to 3 MPa.
When the thermoplastic resin used for the A layer is a polycarbonate resin, the press molding temperature is preferably 230 to 280 ° C, more preferably 240 to 280 ° C, and particularly preferably 250 to 280 ° C. . Further, the pressing pressure is preferably 0.5 to 4.0 MPa, more preferably 0.5 to 3.0 MPa, and particularly preferably 1 to 3 MPa.
By press-molding in such a range, a laminate excellent in the balance between low linear expansion and good surface appearance can be produced.

[Physical properties of this laminate]
In this laminate, the maximum cross-sectional height (Rt) of the surface of the layer A is measured according to JIS B0601 (2013), preferably 3 μm or less, more preferably 2.5 μm or less, and 2 μm. It is particularly preferred that
If the maximum cross-sectional height (Rt) of the surface of the A layer is 3 μm or less, the laminate has a particularly good surface appearance. The maximum cross-sectional height (Rt) of the surface of the A layer is preferably as small as possible, and the lower limit is not particularly defined.
Examples of a method for setting the maximum cross-sectional height (Rt) of the surface of the A layer as the range include the content ratio of the plate-like inorganic particles in the A layer and the maximum diameter of the carbon fiber bundle in the B layer. The method of adjusting in the range specified in (1) is mentioned.

The thickness of the laminate is not particularly limited, but is preferably 1.7 mm or more and 5 mm or less, more preferably 1.7 mm or more and 4 mm or less, and 1.7 mm or more and 3 mm or less. Is particularly preferred.
When the thickness of the laminate is 1.7 mm or more, the laminate and a product obtained by press-molding the laminate are excellent in surface appearance. Moreover, if the thickness of this laminated body is 5 mm or less, this laminated body is excellent in low linear expansion property.

The present laminate is excellent in low thermal expansion properties, JIS K7197 (2012 year) linear expansion coefficient measured in accordance with is preferably at 5 × ^{10 -5} / ℃ less, 1 × 10 ^- More preferably, it is ⁵ / ° C. or less.

  Note that the two A layers included in the laminate need not necessarily have the same thickness using the same thermoplastic resin and plate-like inorganic particles in the same composition, but the thermoplastic resin and the plate-like inorganic particles. , The content ratio of the plate-like inorganic particles, the content ratio of other components, and the like may be different, and the thickness may be different. In terms of uniformity of physical properties in the thickness direction of the laminate, warpage problems, ease of production, etc., the two A layers in the laminate are of the same physical properties or thickness, each made of the same material. It is preferable.

  EXAMPLES Hereinafter, examples for more specifically explaining the present invention will be shown, but the present invention is not limited to the specific modes shown in the examples.

[Measurement / Evaluation]
Measurement and evaluation in Examples and Comparative Examples were performed by the following methods and standards.

(1) Melt mass flow rate According to JIS K7210 (1999), the melt mass flow rate of the thermoplastic resin was measured.

(2) Mw / Mn
Mw / Mn of the thermoplastic resin was measured by a GPC (gel permeation chromatography) method according to JIS K7252-1 (2008).

(3) Maximum diameter of carbon fiber bundle in layer B A cross section in the thickness direction of the produced laminate was observed using an optical microscope. For the B layer, 50 visual fields having a height of 500 μm and a width of 2 mm were arbitrarily observed, and the maximum diameter of the carbon fiber bundle existing in the entire visual field was defined as the maximum diameter of the carbon fiber bundle in the B layer.

(4) Average fiber length of carbon fibers in layer B A cross section in the thickness direction of the produced laminate was observed using an optical microscope. Observe 50 fields of view of height 500 μm x width 2 mm for layer B, measure the length of each carbon fiber in the entire field of view one by one, and the average of this sum is the average fiber of carbon fibers in layer B It was long.

(5) Low linear expansion Using a TMA measuring device 7100 manufactured by Hitachi High-Tech Science Co., Ltd., the linear expansion coefficient from 20 ° C. to 150 ° C. was measured for the produced laminate in accordance with JIS K7197 (2012). Coefficients were calculated and evaluated according to the following criteria.
A: The linear expansion coefficient is 1 × 10 ⁻⁵ / ° C. or less. ○: The linear expansion coefficient is greater than 1 × 10 ⁻⁵ / ° C. and 5 × 10 ⁻⁵ / ° C. or less. X: The linear expansion coefficient is 5 × 10 ⁻⁵ / ° C. Greater than

(6) Surface appearance (maximum cross-sectional height (Rt) of layer A)
The maximum cross-sectional height (Rt) of the surface of layer A of the produced laminate was measured according to JIS B0601 (2013) using a three-dimensional roughness meter manufactured by Kosaka Laboratory Ltd., and evaluated according to the following criteria: did.
○: The maximum cross-sectional height is 3 μm or less. X: The maximum cross-sectional height is larger than 3 μm.

(7) Press formability When the thermoplastic resin used for the A layer is a PP resin using a shaping mold with a step height of 10 mm, the temperature is 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and when the thermoplastic resin used for the A layer is PC resin, press molding is performed under the conditions of temperature = 260 ° C., pressure = 2 MPa, molding time = 15 minutes. The surface of layer A was visually observed and evaluated according to the following criteria.
○: The carbon fiber is not exposed on the surface of the A layer and the crack is not generated. ×: The carbon fiber is exposed on the surface of the A layer, or the laminate cannot follow the shaping die. A state in which cracking occurs.

[Materials used]
The materials used in Examples and Comparative Examples are as follows.

Polypropylene (PP) resin: Novatec PP EA9 (Nippon Polypro Co., Ltd. homopolypropylene, melt mass flow rate (temperature = 230 ° C., load = 2.16 kgf) = 0.5 g / 10 min, Mw / Mn = 5)
Polycarbonate (PC) resin: Caliber 301-30 (Bisphenol-A homopolycarbonate manufactured by Sumika Stylon Co., Ltd., melt mass flow rate (temperature = 300 ° C., load = 1.2 kgf) = 30 g / 10 min)
Plate-like inorganic particles 1 (mica 1): muscovite W400 (manufactured by Kirara Co., Ltd., average particle size = 18 μm, aspect ratio = 35)
Plate-like inorganic particles 2 (mica 2): muscovite 200W (manufactured by Kirara Co., Ltd., average particle size = 100 μm, aspect ratio = 60)
Plate-like inorganic particles 3 (mica 3): muscovite 30-C (manufactured by Kirara Co., Ltd., average particle size = 680 μm, aspect ratio = 90)
Flame retardant: Fire cut P-1590 (Suzuhiro Chemical Co., Ltd. antimony flame retardant + bromine flame retardant)
Lubricant: MS-6 (12-hydroxystearic acid manufactured by Nitto Kasei Kogyo Co., Ltd.)
Antioxidant: IRGANOX B225 (Phosphorus heat stabilizer + hindered phenol antioxidant manufactured by BASF Corporation)
Carbon fiber: DIALEAD K6371T (Mesophase pitch carbon fiber manufactured by Mitsubishi Plastics, Inc.)

[Example 1]
(Preparation of sheet used for layer A)
Mica 1, flame retardant, lubricant, and antioxidant are mixed in proportions shown in Table 1 with respect to 100 parts by mass of PP resin, and supplied to a plastograph mixer manufactured by Toyo Seiki Co., Ltd., temperature = 190 ° C., Melting and kneading were carried out under the conditions of rotational speed = 50 rpm and kneading time = 5 minutes to obtain a resin composition. The obtained resin composition is sandwiched between two metal plates, press molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a plate-like inorganic particle-containing polypropylene resin having a thickness of 0.925 mm A sheet was produced.

(Production of carbon fiber material used for layer B)
The carbon fiber was spread and dispersed by a wet paper making method using a disaggregator according to JIS P8220-1 (2012), and paper was made to prepare a carbon fiber paper having a weight of 100 g / m ² . At this time, the disaggregator was operated under the conditions of propeller rotation speed = 3000 rpm and rotation time = 10 seconds. The obtained carbon fiber paper is referred to as “highly spread paper”.

(Production of laminate)
The sheet used for the layer A and the carbon fiber material used for the layer B are stacked so as to have the structure of layer A / layer B / layer A, and sandwiched between two metal plates. Temperature = 200 ° C., pressure = 2 MPa Then, press molding was carried out under the condition of molding time = 15 minutes to produce a laminate having a thickness of 2 mm. At this time, the thickness of the A layer = 925 μm and the thickness of the B layer = 150 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 2]
In Example 1, a laminate was produced in the same manner except that the content ratio of mica 1 in the sheet used for the A layer was changed as described in Table 1. At this time, the thickness of the A layer = 925 μm and the thickness of the B layer = 150 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 3]
In Example 1, a laminate was produced in the same manner except that the content ratio of mica 1 in the sheet used for the A layer was changed as described in Table 1. At this time, the thickness of the A layer = 925 μm and the thickness of the B layer = 150 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 4]
A laminate was prepared in the same manner as in Example 1, except that mica 1 in the sheet used for the A layer was changed to mica 2. At this time, the thickness of the A layer = 925 μm and the thickness of the B layer = 150 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 5]
A laminate was prepared in the same manner as in Example 1 except that mica 1 in the sheet used for the A layer was changed to mica 3. At this time, the thickness of the A layer = 925 μm and the thickness of the B layer = 150 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 6]
(Preparation of sheets used for other layers)
A PP resin was sandwiched between two metal plates and press molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a polypropylene resin sheet having a thickness of 1 mm was produced.

(Production of laminate)
The sheet used for the other layer produced, the sheet used for the A layer produced in Example 2, and the high-spread paper used for the B layer produced in Example 1 were divided into A layer / B layer / other layer / B Layered / A layered and sandwiched between two metal plates, press-molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes to produce a 2 mm thick laminate did. At this time, the thickness of the A layer = 500 μm, the thickness of the B layer = 150 μm, and the thicknesses of the other layers = 700 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 7]
(Preparation of sheet used for layer A)
Mica 1 is mixed at a ratio shown in Table 1 with respect to 100 parts by mass of PC resin and supplied to a plastograph mixer manufactured by Toyo Seiki Co., Ltd., temperature = 260 ° C., rotation speed = 50 rpm, kneading time = 5. The resin composition was obtained by melt-kneading under the conditions of minutes. The obtained resin composition is sandwiched between two metal plates, press molded under the conditions of temperature = 260 ° C., pressure = 2 MPa, molding time = 15 minutes, and a plate-like inorganic particle-containing polycarbonate resin having a thickness of 0.5 mm. A sheet was produced.

(Preparation of sheets used for other layers)
A PC resin was sandwiched between two metal plates and press molded under the conditions of temperature = 260 ° C., pressure = 2 MPa, molding time = 15 minutes, and a polycarbonate resin sheet having a thickness of 1 mm was produced.

(Production of laminate)
The sheet used for the produced A layer and other layers and the high spread paper used for the B layer produced in Example 1 are configured to be A layer / B layer / other layers / B layer / A layer. The laminate was sandwiched between two metal plates and press-molded under the conditions of temperature = 260 ° C., pressure = 2 MPa, molding time = 15 minutes, and a 2 mm-thick laminate was produced. At this time, the thickness of the A layer = 500 μm, the thickness of the B layer = 150 μm, and the thicknesses of the other layers = 700 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Example 8]
(Preparation of sheets used for other layers)
Mica 1, flame retardant, lubricant, and antioxidant are mixed in proportions shown in Table 1 with respect to 100 parts by mass of PP resin, and supplied to a plastograph mixer manufactured by Toyo Seiki Co., Ltd., temperature = 190 ° C., Melting and kneading were carried out under the conditions of rotational speed = 50 rpm and kneading time = 5 minutes to obtain a resin composition. The obtained resin composition was sandwiched between two metal plates and press molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a 1 mm thick plate-like inorganic particle-containing polypropylene resin sheet was obtained. Produced.

(Production of laminate)
The sheet used for the other layer produced, the sheet used for the A layer produced in Example 2, and the high-spread paper used for the B layer produced in Example 1 were divided into A layer / B layer / other layer / B Layered / A layered and sandwiched between two metal plates, press-molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes to produce a 2 mm thick laminate did. At this time, the thickness of the A layer = 500 μm, the thickness of the B layer = 150 μm, and the thicknesses of the other layers = 700 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Comparative Example 1]
A PP resin was sandwiched between two metal plates and press-molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a single-layer polypropylene resin sheet having a thickness of 2 mm was produced.
The obtained sheet was evaluated and the results are shown in Table 1.

[Comparative Example 2]
As a sheet used for the A layer, a PP resin is sandwiched between two metal plates, press-molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a polypropylene resin sheet having a thickness of 0.5 mm is obtained. Produced.
The high-spreading paper used for the B layer as in Example 1 and the sheet used for the other layers as in Example 6 were prepared, and the configuration of A layer / B layer / other layer / B layer / A layer Then, the laminate was sandwiched between two metal plates and press-molded under the conditions of temperature = 200 ° C., pressure = 2 MPa, molding time = 15 minutes, and a laminate having a thickness of 2 mm was produced. At this time, the thickness of the A layer = 425 μm, the thickness of the B layer = 150 μm, and the thicknesses of the other layers = 850 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Comparative Example 3]
Mica 1, a flame retardant, a lubricant, and an antioxidant were mixed at a ratio shown in Table 1 with respect to 100 parts by mass of the PP resin to prepare a sheet used for the A layer in the same manner as in Example 1.
Next, in the production of the carbon fiber material used for the B layer, a carbon fiber paper was produced in the same manner as in Example 1 except that the disintegrator was operated under the conditions of the rotation speed of the propeller = 500 rpm and the rotation time = 10 seconds. . This carbon fiber paper is referred to as “low spread paper”.
The sheet | seat used for another layer similarly to Example 6 is produced, it piles up so that it may become a structure of A layer / B layer / other layer / B layer / A layer, and is pinched | interposed between two metal plates, temperature = The laminate was press-molded under the conditions of 200 ° C., pressure = 2 MPa, and molding time = 15 minutes to produce a laminate having a thickness of 2 mm. At this time, the thickness of the A layer = 500 μm, the thickness of the B layer = 150 μm, and the thickness of the C layer = 700 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Comparative Example 4]
Mica 1, a flame retardant, a lubricant, and an antioxidant were mixed at a ratio shown in Table 1 with respect to 100 parts by mass of the PP resin to prepare a sheet used for the A layer in the same manner as in Example 1.
Next, in the production of the carbon fiber material used for the B layer, a carbon fiber paper was produced in the same manner as in Example 1 except that the disintegrator was operated under the conditions of the rotation speed of the propeller = 1000 rpm and the rotation time = 10 seconds. . This carbon fiber paper is referred to as “standard spread paper”.
The sheet | seat used for another layer similarly to Example 6 is produced, it piles up so that it may become a structure of A layer / B layer / other layer / B layer / A layer, and is pinched | interposed between two metal plates, temperature = The laminate was press-molded under the conditions of 200 ° C., pressure = 2 MPa, and molding time = 15 minutes to produce a laminate having a thickness of 2 mm. At this time, the thickness of the A layer = 500 μm, the thickness of the B layer = 150 μm, and the thicknesses of the other layers = 700 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Comparative Example 5]
Mica 1, a flame retardant, a lubricant, and an antioxidant were mixed at a ratio shown in Table 1 with respect to 100 parts by mass of the PP resin to prepare a sheet used for the A layer in the same manner as in Example 1.
A sheet used for other layers was prepared in the same manner as in Example 6, and was stacked between two metal plates so as to have a configuration of A layer / other layers / A layer, temperature = 200 ° C., pressure = 2 MPa. Then, press molding was carried out under the condition of molding time = 15 minutes to produce a laminate having a thickness of 2 mm. At this time, the thickness of the A layer was 500 μm, and the thicknesses of the other layers were 1000 μm.
The obtained laminate was evaluated and the results are shown in Table 1.

[Comparative Example 6]
Mica 1, a flame retardant, a lubricant, and an antioxidant were mixed at a ratio shown in Table 1 with respect to 100 parts by mass of PP resin, and an attempt was made to produce a sheet used for layer A in the same manner as in Example 1. The content ratio of was too large to obtain a sheet.

As shown in Table 1, the carbon fiber composite laminate of the present invention produced in the examples has an excellent balance between low linear expansion, good surface appearance and press formability.
On the other hand, those produced in the comparative examples do not satisfy the ranges specified in the present invention, the maximum diameter of the carbon fiber bundle, the average fiber length of the carbon fiber, low linear expansion, surface appearance, and press formability. At least one of them was insufficient.

  This laminate is a carbon fiber composite laminate that has an excellent balance of low linear expansion, good surface appearance and press formability, and can meet the demands for light weight and low cost. It can be suitably used for various molded products such as product casings, automobile and railway interior materials and exterior materials.

Claims (4)

  A carbon fiber composite laminate having at least a three-layer structure, comprising 30 to 200 parts by mass of plate-like inorganic particles having an aspect ratio of 20 to 500 with respect to 100 parts by mass of the thermoplastic resin. It has a plastic resin layer (A layer) and a carbon fiber layer (B layer), the A layer is a front and back layer, the maximum diameter of the carbon fiber bundle in the B layer is 10 μm or more, 1000 μm or less, And the carbon fiber composite laminated body whose average fiber length of this carbon fiber is 0.1 mm or more and less than 5 mm.   The carbon fiber composite laminate according to claim 1, wherein the thermoplastic resin used for the A layer is at least one resin selected from the group consisting of polyolefin resins, polycarbonate resins, polyamide resins, and polyester resins. body.   The carbon fiber composite laminate according to claim 1 or 2, wherein the B layer is a layer formed by using a carbon fiber mat or carbon fiber paper as a carbon fiber material.   The carbon fiber composite laminate according to any one of claims 1 to 3, wherein a maximum cross-sectional height (Rt) of the surface of the A layer is 3 µm or less.