JPWO2017038421A1 - Liquid crystalline resin composition for camera module and camera module using the same - Google Patents

Abstract

Provided a liquid crystalline resin composition for a camera module that has high fluidity when melted, used to produce parts for a camera module that have a hard-to-brush surface, low warpage, high mechanical strength, and excellent heat resistance. To do. The liquid crystalline resin composition for a camera module according to the present invention contains (A) liquid crystalline resin, (B) fibrous wollastonite, (C) an epoxy group-containing copolymer, and (D) a plate-like filler. The content of the component (A) is 55 to 95.5% by mass, the content of the component (B) is 2.5 to 25% by mass, and the content of the component (C) is 1.0 to 4.5% by mass. %, The content of the component (D) is 10 to 35% by mass, and the total content of the component (B) and the component (D) is 20 to 37.5% by mass.

Description

  The present invention relates to a liquid crystalline resin composition for a camera module and a camera module using the same.

  Liquid crystalline resins typified by liquid crystalline polyester resins have excellent mechanical strength, heat resistance, chemical resistance, electrical properties, etc. in a well-balanced manner and have excellent dimensional stability. It's being used. Recently, liquid crystal resins have been used for precision equipment parts by taking advantage of these features.

  In the case of precision equipment, particularly optical equipment with a lens, slight dust, dust, etc. affect the performance of the equipment. For example, in a part used in an optical device such as a camera module, if small dust, oil, or dust adheres to the lens, the optical characteristics of the camera module are significantly deteriorated. In order to prevent such deterioration of optical characteristics, the parts that make up the camera module (hereinafter sometimes referred to as “camera module parts”) are ultrasonically cleaned before being assembled and attached to the surface. Small dust, oil, dust, etc. are removed.

  As described above, the molded body formed by molding the liquid crystalline resin composition is easy to peel off because the molecular orientation of the polymer is particularly large in the surface portion. The fluffing phenomenon of peeling and fluffing occurs, and the fluffed raised portion causes small dust.

  Therefore, when the liquid crystalline resin composition is used as a raw material for camera module parts, a special liquid crystalline resin composition is used in which the surface of the molded body is not raised even when the molded body is ultrasonically cleaned. As a special liquid crystalline resin composition, a liquid crystalline resin composition for a camera module containing a liquid crystalline resin, a specific talc, and carbon black is disclosed (see Patent Document 1).

JP 2009-242453 A

  However, according to the study by the present inventors, the liquid crystalline resin composition for a camera module described in Patent Document 1 has insufficient suppression of raising of the surface of the molded article, and the molded article is more difficult to raise the surface of the molded article. A liquid crystalline resin composition for a camera module for manufacturing the above is required.

  Further, according to the study by the present inventors, when a molded product such as a lens holder is manufactured by molding a conventional liquid crystalline resin composition for a camera module, warpage deformation is large, causing problems when the camera module is assembled. There was a thing.

  Furthermore, in recent years, mobile phones equipped with a camera module and a function equivalent to a non-contact type IC card have become widespread. Such a cellular phone is held over a non-contact type reader when reading and writing information. At that time, since the mobile phone may collide with the non-contact type reader with a strong force, a camera for manufacturing a molded body having high mechanical strength so that the camera module in the mobile phone is less likely to be defective. A liquid crystalline resin composition for modules is required.

  In addition, a liquid crystalline resin composition for a camera module for producing a molded article having excellent heat resistance is required from the viewpoint of making it difficult to cause problems during processing and use of the camera module.

  In addition, the liquid crystalline resin composition for camera modules is required to have high fluidity when melted from the viewpoint of moldability.

  The present invention has been made in order to solve the above-mentioned problems, and its purpose is to produce a camera module component that has a surface that is less likely to be raised, is prevented from warping, has high mechanical strength, and is excellent in heat resistance. Another object of the present invention is to provide a liquid crystalline resin composition for a camera module that is used in the above and has high fluidity when melted.

  The inventors of the present invention have made extensive studies to solve the above problems. As a result, the liquid crystal resin, the fibrous wollastonite, the epoxy group-containing copolymer, and the plate-like filler are used in a specific ratio to solve the above problems. The present inventors have found that this can be done and have completed the present invention. More specifically, the present invention provides the following.

(1) (A) Liquid crystalline resin,
(B) Fibrous wollastonite,
(C) an epoxy group-containing copolymer, and (D) a plate-like filler,
The content of the component (A) is 55 to 95.5% by mass, the content of the component (B) is 2.5 to 25% by mass, the content of the component (C) is 1.0 to 4.5% by mass, (D) The liquid crystalline resin composition for camera modules whose content of a component is 10-35 mass% and whose total content of (B) component and (D) component is 20-37.5 mass%.

  (2) The (C) epoxy group-containing copolymer is at least one selected from the group consisting of (C1) an epoxy group-containing olefin copolymer and (C2) an epoxy group-containing styrene copolymer. The composition according to (1).

  (3) A camera module part comprising the composition according to (1) or (2).

  (4) A camera module comprising the component according to (3).

  The liquid crystalline resin composition for a camera module of the present invention has high fluidity at the time of melting. When a camera module part is produced using this composition as a raw material, the surface is hardly raised and warpage deformation is suppressed. Camera module parts with high strength and excellent heat resistance can be obtained.

It is sectional drawing which shows a common camera module typically.

  Hereinafter, embodiments of the present invention will be described. In addition, this invention is not limited to the following embodiment.

<Liquid crystal resin composition for camera module>
The liquid crystalline resin composition for a camera module of the present invention contains (A) liquid crystalline resin, (B) fibrous wollastonite, (C) an epoxy group-containing copolymer, and (D) a plate-like filler. .

[(A) Liquid crystalline resin]
The (A) liquid crystalline resin used in the present invention refers to a melt processable polymer having a property capable of forming an optically anisotropic molten phase. The property of the anisotropic molten phase can be confirmed by a conventional polarization inspection method using an orthogonal polarizer. More specifically, the anisotropic molten phase can be confirmed by using a Leitz polarizing microscope and observing a molten sample placed on a Leitz hot stage under a nitrogen atmosphere at a magnification of 40 times. When the liquid crystalline polymer applicable to the present invention is inspected between crossed polarizers, the polarized light is normally transmitted even in the molten stationary state, and optically anisotropic.

  The kind of the above (A) liquid crystalline resin is not particularly limited, and is preferably an aromatic polyester and / or an aromatic polyester amide. Moreover, the polyester which partially contains aromatic polyester and / or aromatic polyester amide in the same molecular chain is also within the range. (A) The liquid crystalline resin is preferably at least about 2.0 dl / g, more preferably 2.0 to 10.0 dl / g when dissolved in pentafluorophenol at 60 ° C. at a concentration of 0.1% by mass. Those having a logarithmic viscosity (IV) of 1 are preferably used.

  The aromatic polyester or aromatic polyester amide as the liquid crystalline resin (A) applicable to the present invention is particularly preferably at least one selected from the group consisting of aromatic hydroxycarboxylic acids, aromatic hydroxyamines, and aromatic diamines. An aromatic polyester or aromatic polyester amide having a repeating unit derived from a seed compound as a constituent component.

More specifically,
(1) A polyester mainly composed of repeating units derived from one or more aromatic hydroxycarboxylic acids and derivatives thereof;
(2) Mainly (a) a repeating unit derived from one or more of aromatic hydroxycarboxylic acids and derivatives thereof, and (b) one of aromatic dicarboxylic acids, alicyclic dicarboxylic acids, and derivatives thereof Or a polyester comprising a repeating unit derived from two or more and (c) a repeating unit derived from at least one or more of aromatic diol, alicyclic diol, aliphatic diol, and derivatives thereof;
(3) a repeating unit mainly derived from (a) one or more of an aromatic hydroxycarboxylic acid and a derivative thereof; and (b) one or two of an aromatic hydroxyamine, an aromatic diamine, and a derivative thereof. A polyesteramide comprising a repeating unit derived from at least one species and (c) a repeating unit derived from one or more of aromatic dicarboxylic acid, alicyclic dicarboxylic acid, and derivatives thereof;
(4) a repeating unit mainly derived from (a) one or more of aromatic hydroxycarboxylic acids and derivatives thereof; and (b) one or two of aromatic hydroxyamines, aromatic diamines and derivatives thereof. A repeating unit derived from more than one species, (c) a repeating unit derived from one or more of aromatic dicarboxylic acid, alicyclic dicarboxylic acid and derivatives thereof, and (d) aromatic diol, alicyclic And polyester amides composed of a repeating unit derived from at least one or more of an aliphatic diol, an aliphatic diol, and derivatives thereof. Furthermore, you may use a molecular weight regulator together with said structural component as needed.

（Ｘ：アルキレン（Ｃ_１〜Ｃ_４）、アルキリデン、−Ｏ−、−ＳＯ−、−ＳＯ_２−、−Ｓ−、及び−ＣＯ−より選ばれる基である）

（Ｙ：−（ＣＨ_２）_ｎ−（ｎ＝１〜４）及び−Ｏ（ＣＨ_２）_ｎＯ−（ｎ＝１〜４）より選ばれる基である。）Preferable examples of the specific compound constituting the liquid crystalline resin (A) applicable to the present invention include aromatic hydroxycarboxylic acids such as p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid, and 2,6-dihydroxy. Aromatic diols such as naphthalene, 1,4-dihydroxynaphthalene, 4,4′-dihydroxybiphenyl, hydroquinone, resorcin, a compound represented by the following general formula (I), and a compound represented by the following general formula (II) Aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, 4,4′-diphenyldicarboxylic acid, 2,6-naphthalenedicarboxylic acid, and compounds represented by the following general formula (III); p-aminophenol, p- Aromatic amines such as phenylenediamine are listed.

(X is a group selected from alkylene (C _{1 to} C ₄ ), alkylidene, —O—, —SO—, —SO ₂ —, —S—, and —CO—)

(Y is a group selected from — (CH ₂ ) _n — (n = 1 to 4) and —O (CH ₂ ) _n O— (n = 1 to 4).

The (A) liquid crystalline resin used in the present invention can be prepared from the above monomer compound (or a mixture of monomers) by a known method using a direct polymerization method or a transesterification method, and usually a melt polymerization method. Or a slurry polymerization method. The above compounds having ester-forming ability may be used for polymerization in the form as they are, or may be modified from a precursor to a derivative having ester-forming ability in the previous stage of polymerization. In the polymerization, various catalysts can be used. Typical examples include dialkyl tin oxide, diaryl tin oxide, titanium dioxide, alkoxy titanium silicates, titanium alcoholates, and alkali of carboxylic acid. And alkaline earth metal salts, Lewis acid salts such as BF _{3 and} the like. The amount of the catalyst used is generally about 0.001 to 1% by weight, particularly about 0.01 to 0.2% by weight, based on the total weight of the monomers. If the polymer produced by these polymerization methods is further necessary, the molecular weight can be increased by solid-phase polymerization by heating in a reduced pressure or an inert gas.

The melt viscosity of the (A) liquid crystalline resin obtained by the above method is not particularly limited. Generally, those having a melt viscosity at a molding temperature of 10 MPa or more and 600 MPa or less at a shear rate of 1000 sec ⁻¹ can be used. However, those having a very high viscosity are not preferable because the fluidity is extremely deteriorated. The (A) liquid crystalline resin may be a mixture of two or more liquid crystalline resins.

  In the liquid crystalline resin composition for a camera module of the present invention, the content of (A) liquid crystalline resin is 55 to 95.5% by mass. If the content of the component (A) is 55% by mass or more, it is preferable because of fluidity and suppression of raising of the surface of the molded body, and if the content of the component (A) is 95.5% by mass or less, the reason is heat resistance. Is preferable. Moreover, preferable content of (A) component is 60-80 mass%, and more preferable content of (A) component is 62-70 mass%.

[(B) Fibrous wollastonite]
In the present specification, (B) fibrous wollastonite means wollastonite having an aspect ratio, that is, an average fiber length / average fiber diameter value of 8 or more. The aspect ratio is preferably 10 to 25 and more preferably 15 to 20 from the viewpoint of the effect of suppressing the raising of the surface of the molded body. In the present specification, wollastonite having an aspect ratio of less than 8 is referred to as granular wollastonite.

  (B) It does not specifically limit as fibrous wollastonite, For example, a well-known fibrous wollastonite can be used. (B) A fibrous wollastonite may be used individually by 1 type, and may be used in combination of 2 or more types from which an aspect ratio, an average fiber length, an average fiber diameter, etc. differ.

  (B) The average fiber diameter of fibrous wollastonite is preferably 3.0 to 50 μm, and more preferably 4.5 to 40 μm. When the average fiber diameter is 3.0 μm or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured. When the average fiber diameter is 50 μm or less, the effect of suppressing napping on the surface of the molded body tends to be high. In the present specification, as the average fiber diameter, a value obtained by capturing a stereoscopic microscope image from a CCD camera into a PC and measuring the image by an image processing method is employed.

  (B) The average fiber length of the fibrous wollastonite is preferably 30 to 800 μm, and more preferably 50 to 600 μm. When the average fiber length is 30 μm or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured. When the average fiber length is 800 μm or less, the effect of suppressing napping on the surface of the molded body tends to increase. In this specification, as the average fiber length, a value obtained by taking a stereoscopic microscope image from a CCD camera into a PC and measuring by an image processing method using an image measuring machine is adopted.

  (B) Content of a component is 2.5-25 mass% in the liquid crystalline composition for camera modules of this invention. When the content of the component (B) is 2.5% by mass or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured. When the content of the component (B) is 25% by mass or less, the fluidity at the time of melting the composition is easily improved, the effect of suppressing the raising of the surface of the molded body is likely to be high, and the effect of suppressing warpage deformation of the molded body is high. Prone. More preferably, the content is 5 to 20% by mass.

[(C) Epoxy group-containing copolymer]
(C) The epoxy group-containing copolymer can be used alone or in combination of two or more. The (C) epoxy group-containing copolymer is not particularly limited. For example, at least selected from the group consisting of (C1) an epoxy group-containing olefin copolymer and (C2) an epoxy group-containing styrene copolymer. One type is mentioned. Mixing the component (C) with the liquid crystalline resin composition for a camera module contributes to suppressing raising of the surface of the molded product when the molded product obtained by molding the composition is subjected to ultrasonic cleaning.
The reason for suppressing the raising is not clarified, but it is considered that by adding a certain amount, the surface state of the molded body is changed, and the change contributes to suppressing the raising.

  Examples of the (C1) epoxy group-containing olefin copolymer include a copolymer composed of a repeating unit derived from an α-olefin and a repeating unit derived from a glycidyl ester of an α, β-unsaturated acid. It is done.

The α-olefin is not particularly limited, and examples thereof include ethylene, propylene, and butene. Among them, ethylene is preferably used. The glycidyl ester of α, β-unsaturated acid is represented by the following general formula (IV). Examples of the glycidyl ester of α, β-unsaturated acid are glycidyl acrylate, glycidyl methacrylate, glycidyl ethacrylate, glycidyl itaconate, and the like, and glycidyl methacrylate is particularly preferable.

  (C1) In the epoxy group-containing olefin copolymer, the content of the repeating unit derived from α-olefin is 87 to 98% by mass, and the content of the repeating unit derived from glycidyl ester of α, β-unsaturated acid The amount is preferably 13-2% by mass.

  The (C1) epoxy group-containing olefin copolymer used in the present invention is an acrylonitrile, acrylic ester, methacrylic ester, α-methylstyrene, anhydrous maleic as a third component in addition to the two components as long as the present invention is not impaired. You may contain 0-48 mass parts of repeating units derived from 1 type, or 2 or more types of olefin type unsaturated esters, such as an acid, with respect to 100 mass parts of said 2 components.

  The epoxy group-containing olefin copolymer which is the component (C1) of the present invention can be easily prepared by a normal radical polymerization method using a monomer and a radical polymerization catalyst corresponding to each component. More specifically, usually an α-olefin and a glycidyl ester of an α, β-unsaturated acid are present in the presence of a radical generator at 500 to 4000 atmospheres and 100 to 300 ° C. in the presence of a suitable solvent or chain transfer agent. It can be produced by a method of copolymerization under or in the absence. It can also be produced by a method in which an α-olefin, a glycidyl ester of α, β-unsaturated acid and a radical generator are mixed and subjected to melt graft copolymerization in an extruder.

  Examples of the epoxy group-containing styrenic copolymer (C2) include a copolymer composed of a repeating unit derived from styrene and a repeating unit derived from a glycidyl ester of an α, β-unsaturated acid. It is done. Since the glycidyl ester of α, β-unsaturated acid is the same as that described in the component (C1), the description thereof is omitted.

  Examples of styrenes include styrene, α-methylstyrene, brominated styrene, divinylbenzene and the like, and styrene is preferably used.

  The (C2) epoxy group-containing styrene copolymer used in the present invention is a multi-component copolymer containing a repeating unit derived from one or more other vinyl monomers as a third component in addition to the above two components. There may be. Suitable as the third component is a repeating unit derived from one or more olefinic unsaturated esters such as acrylonitrile, acrylic acid ester, methacrylic acid ester, and maleic anhydride. An epoxy group-containing styrene copolymer containing 40% by mass or less of these repeating units in the copolymer is preferred as the component (C2).

  (C2) In the epoxy group-containing styrene copolymer, the content of the repeating unit derived from the glycidyl ester of α, β-unsaturated acid is 2 to 20% by mass, and the content of the repeating unit derived from styrenes Is preferably 80 to 98% by mass.

  (C2) The epoxy group-containing styrene-based copolymer can be prepared by a normal radical polymerization method using a monomer corresponding to each component and a radical polymerization catalyst. More specifically, styrenes and glycidyl esters of α, β-unsaturated acids are usually present in the presence of a radical generator at 500 to 4000 atm and 100 to 300 ° C. in the presence of a suitable solvent or chain transfer agent. Or it can manufacture by the method of copolymerizing in absence. It can also be produced by a method in which styrenes, a glycidyl ester of an α, β-unsaturated acid and a radical generator are mixed and subjected to melt graft copolymerization in an extruder.

  As the (C) epoxy group-containing copolymer, (C1) an epoxy group-containing olefin copolymer is preferable from the viewpoint of heat resistance. When the component (C1) and the component (C2) are used in combination, the ratio between these components can be appropriately selected according to the required characteristics.

  (C) Content of an epoxy group containing copolymer is 1.0-4.5 mass% in the resin composition for camera modules of this invention. The content of the component (C) is 1.0% by mass or more from the viewpoint of suppressing raising of the surface of the molded body, and 4.5% by mass or less is good without impairing fluidity. Necessary for the reason of obtaining a molded body. More preferably, the content is 2.0 to 4.0% by mass.

[(D) Plate-like filler]
(D) The plate-like filler preferably has an average particle size of 20 to 50 μm. When the average particle diameter is 20 μm or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured, and the warpage deformation suppressing effect of the molded body is likely to increase. When the average particle size is 50 μm or less, the effect of suppressing napping on the surface of the molded body tends to increase. The average particle diameter is preferably 23 to 30 μm. In this specification, the value measured by the laser diffraction / scattering particle size distribution measurement method is adopted as the average particle size.

  (D) It does not specifically limit as a plate-shaped filler, For example, mica, talc, glass flake, graphite, various metal foils (for example, aluminum foil, iron foil, copper foil) etc. are mentioned. As the component (D), two or more kinds may be used. In the present invention, mica and talc are preferably used as the component (D), and mica is more preferably used.

  (D) Content of a component is 10-35 mass% in the liquid crystalline composition for camera modules of this invention. When the content of the component (D) is 10% by mass or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured, and the warpage deformation suppressing effect of the molded body is likely to increase. When the content of the component (D) is 35% by mass or less, the effect of suppressing the raising of the surface of the molded body tends to be high. The above-mentioned content is preferably 15 to 30% by mass.

  Furthermore, the total content of the component (B) and the component (D) is 20 to 37.5% by mass, preferably 25 to 35% by mass in the liquid crystal composition for a camera module of the present invention. . When the total content is 20% by mass or more, the mechanical strength and the deflection temperature under load necessary for the camera module are easily secured. When the total content is 37.5% by mass or less, the fluidity at the time of melting of the composition is easily improved, the effect of suppressing the raising of the surface of the molded body is easily increased, and the impact resistance of the molded body is increased. Cheap.

[(E) Carbon black]
The carbon black (E) used as an optional component in the present invention is not particularly limited as long as it is generally available for use in resin coloring. Normally, (E) carbon black contains a lump formed by agglomeration of primary particles, but the resin composition of the present invention is molded unless a large amount of lump having a size of 50 μm or more is contained. Many bumps (fine bumpy projections (fine irregularities) in which carbon black is aggregated) hardly occur on the surface of the molded body. When the content of particles having a lump particle diameter of 50 μm or more is 20 ppm or less, the effect of suppressing napping on the surface of the molded product tends to be high. A preferable content rate is 5 ppm or less.

  (E) As a compounding quantity of carbon black, the range of 0.5-5 mass% is preferable in the liquid crystalline resin composition for camera modules. When the blending amount of the carbon black is 0.5% by mass or more, the jetness of the obtained resin composition is not easily lowered, and the light shielding property is less likely to be anxious. When the blending amount of the carbon black is 5% by mass or less, it is difficult to be uneconomical, and it is difficult to generate bumps.

[Other ingredients]
The liquid crystalline resin composition for a camera module of the present invention includes other polymers, other fillers, known substances generally added to synthetic resins, that is, antioxidants, as long as the effects of the present invention are not impaired. Stabilizers such as UV absorbers, antistatic agents, flame retardants, colorants such as dyes and pigments, lubricants, mold release agents, crystallization accelerators, crystal nucleating agents, etc. may be added as appropriate according to the required performance. it can.

  Other fillers refer to fillers other than (B) fibrous wollastonite, (D) plate-like filler, and (E) carbon black, such as wollastonite having an aspect ratio of less than 8. (B) Wollastonites other than fibrous wollastonite; (B) Fibrous fillers other than fibrous wollastonite, such as glass fibers; and particulate fillers such as silica.

[Preparation of liquid crystalline resin composition for camera module]
The preparation of the resin composition for a camera module of the present invention is not particularly limited. For example, by blending the above components (A), (B), (C), and (D), and melt-kneading these using a single screw or twin screw extruder, a liquid crystalline resin for a camera module Preparation of the composition takes place.

[Liquid crystalline resin composition for camera modules]
The shape of the component (B) in the liquid crystalline resin composition for a camera module of the present invention is different from the shape of the component (B) before blending. The shape of the above component (B) is the shape before blending. If the shape before blending is as described above, a camera module component that is less prone to raising the surface is obtained.

  Similarly, the shape of (D) component in the liquid crystalline resin composition for camera modules of this invention and the shape of (D) component before mix | blending are different. The shape of the above component (D) is the shape before blending. If the shape before blending is as described above, a camera module component in which warpage deformation is suppressed can be obtained.

The liquid crystalline resin composition for a camera module of the present invention obtained as described above preferably has a melt viscosity of less than 50 Pa · sec. One of the characteristics of the liquid crystalline resin composition for a camera module of the present invention is that the fluidity at the time of melting is high and the moldability is excellent. In this specification, as the melt viscosity, a value obtained by a measurement method based on ISO 11443 under conditions of a cylinder temperature 10 to 20 ° C. higher than the melting point of the liquid crystalline resin and a shear rate of 1000 sec ⁻¹ is adopted.

  The liquid crystalline resin composition for a camera module of the present invention preferably has a deflection temperature under load of 240 ° C. or higher. The point which is excellent in heat resistance is also one of the characteristics of the liquid crystalline resin composition for camera modules of this invention. In addition, the value measured by the method based on ISO75-1 and 2 is employ | adopted for deflection temperature under load.

<Camera module parts and camera module>
A camera module component is manufactured using the liquid crystalline resin composition for a camera module. If the resin composition of this invention is used as a raw material, it will become difficult to raise the surface of the components for camera modules. Since the camera module component is ultrasonically cleaned, it is required that the surface is not easily raised even if the ultrasonic cleaning is performed. If the resin composition of the present invention is used, even if the ultrasonic cleaning of camera module parts is performed under stronger conditions, there will be no or almost no dropouts causing dust and the like. Accordingly, after the camera module parts are incorporated into the finished product, the dust generated by raising the surface of the camera module parts hardly affects the quality of the finished product.

  A camera module component formed by molding the liquid crystalline resin composition for a camera module of the present invention will be described. A cross section of a general camera module is schematically shown in FIG. As shown in FIG. 1, the camera module 1 includes a substrate 10, an optical element 11, a lead wire 12, a lens holder 13, a barrel 14, a lens 15, an IR filter 16, and a guide 17.

  The optical element 11 is disposed on the substrate 10, and the optical element 11 and the substrate 10 are electrically connected by a lead wiring 12.

  The guide 17 is disposed on the substrate 10, the lens holder 13 is disposed on the guide 17, and the guide 17 and the lens holder 13 cover the optical element 11. The lens holder 13 has an opening at the top, and a spiral groove is formed on the wall surface of the opening.

  The barrel 14 has a cylindrical shape, and the lens 15 is held inside the cylindrical shape so as to be substantially horizontal. In addition, a spiral convex portion is formed on the side wall of one end of the cylinder, and this spiral convex portion and the spiral groove portion formed on the opening wall surface of the lens holder 13 are screwed together, The barrel 14 is connected to the lens holder 13. An IR filter 16 is disposed at one end of the barrel 14 so as to close one end of the cylindrical barrel 14. As shown in FIG. 1, the IR filter 16 and the lens 15 are arranged substantially in parallel.

  In the camera module 1 as shown in FIG. 1, the lens holder 13 includes a magnetic force generated by a coil (not shown) wound around the lens holder 13 and a permanent magnet (not shown) arranged around the coil. The distance between the lens 15 and the optical element 11 changes by moving up and down on the guide 17 by the action of. The focus of the camera can be adjusted by adjusting this distance.

  In the camera module 1 as described above, the lens holder 13 and / or the barrel 14 which are parts for the camera module can be manufactured using the liquid crystalline resin composition for a camera module of the present invention as a raw material. A general liquid crystalline resin composition is not suitable as a raw material for producing these parts. When the lens holder 13 and / or the barrel 14 are manufactured using a general liquid crystalline resin composition as a raw material, the following problems occur.

  A molded body formed by molding a general liquid crystalline resin composition has a particularly high molecular orientation of the polymer at the surface portion, so that the surface of the molded body is easily raised, and this raising causes generation of small dust. If this small dust adheres to the lens 15 or the like, the performance of the camera module is degraded.

  Camera module parts such as the lens holder 13 and the barrel 14 are ultrasonically cleaned before being assembled into the camera module 1 for the purpose of removing dust and small dust on the surface. However, since the surface of a molded product formed by molding a general liquid crystalline resin composition is easily raised, the surface becomes fluffy when ultrasonically cleaned. Since such a problem arises, the molded object formed by shape | molding a liquid crystalline resin composition cannot usually be ultrasonically cleaned.

  The focus adjustment is performed on the guide 17 by the action of the magnetic force generated by the coil (not shown) wound around the lens holder 13 and the permanent magnet (not shown) arranged around the coil. It is done by moving up and down. At this time, since the surface of the molded body formed by molding a general liquid crystalline resin composition is likely to be raised as described above, the surface may be peeled off to produce a peeled material. There is a high possibility that the peeled material becomes small dust and adheres to the lens 15 or the like, thereby reducing the performance of the camera module.

  As described above, usually, when the liquid crystalline resin composition is used as a raw material for the lens holder 13 and / or the barrel 14, problems are likely to occur. However, when the liquid crystalline resin composition for a camera module of the present invention is formed into a molded body, Since the surface state of the molded body has been improved so that even if the molded body is ultrasonically cleaned, the problem of raising the hair hardly occurs, it can be preferably used as a raw material for the lens holder 13 and / or the barrel 14.

  When the liquid crystalline resin composition for a camera module of the present invention is used for the lens holder 13, examples of the material for the guide 17 include materials other than the liquid crystalline resin composition for a camera module of the present invention. Etc.

  EXAMPLES Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited only to these examples.

<Liquid crystal resin>
-Liquid crystalline polyesteramide resin The following raw materials were charged in a polymerization vessel, and then the temperature of the reaction system was raised to 140 ° C and reacted at 140 ° C for 1 hour. Thereafter, the temperature is further raised to 340 ° C. over 4.5 hours, and then the pressure is reduced to 10 Torr (ie, 1330 Pa) over 15 minutes while acetic acid, excess acetic anhydride, and other low-boiling components are distilled off. Melt polymerization was performed. After the stirring torque reached a predetermined value, nitrogen was introduced and the pressure was changed from the reduced pressure state to the normal pressure state, the polymer was discharged from the lower part of the polymerization vessel, and the strands were pelletized to obtain pellets. The obtained pellets were heat-treated at 300 ° C. for 2 hours under a nitrogen stream to obtain the target polymer. The obtained polymer had a melting point of 334 ° C. and a melt viscosity of 14.0 Pa · s. The melt viscosity of the polymer was measured in the same manner as the melt viscosity measurement method described later.
(I) 4-hydroxybenzoic acid; 188.4 g (60 mol%)
(II) 2-hydroxy-6-naphthoic acid; 21.4 g (5 mol%)
(III) terephthalic acid; 66.8 g (17.7 mol%)
(IV) 4,4′-dihydroxybiphenyl; 52.2 g (12.3 mol%)
(V) 4-acetoxyaminophenol; 17.2 g (5 mol%)
Metal catalyst (potassium acetate catalyst); 15 mg
Acylating agent (acetic anhydride); 226.2 g

<Material other than liquid crystalline resin>
-Fibrous wollastonite: NYGLOS 8 (manufactured by NYCO Materials, aspect ratio 17, average fiber length 136 μm, average fiber diameter 8 μm)
Granular wollastonite: NYAD 325 (manufactured by NYCO Materials, aspect ratio 5, average fiber length 50 μm, average fiber diameter 5 μm)
Glass fiber: PF70E-001 (manufactured by Nittobo Co., Ltd., milled fiber, average fiber diameter 10 μm, average fiber length 70 μm)
Epoxy group-containing olefin copolymer: Bond First 2C (manufactured by Sumitomo Chemical Co., Ltd., ethylene-glycidyl methacrylate copolymer, glycidyl methacrylate content 6 mass%)
-Epoxy group-free copolymer: Tuftec M1913 (manufactured by Asahi Kasei Corporation, maleic anhydride-modified hydrogenated styrene-ethylene-butadiene-styrene block copolymer)
Plate filler 1: AB-25S (manufactured by Yamaguchi Mica Industry Co., Mica, average particle size 24 μm)
Plate filler 2: Crown talc PP (manufactured by Matsumura Sangyo Co., Ltd., talc, average particle size 12.8 μm, average aspect ratio 6)
Carbon black: VULCAN XC305 (manufactured by Cabot Japan Co., Ltd., average particle size 20 nm, ratio of particles having a particle size of 50 μm or more is 20 ppm or less)

<Manufacture of liquid crystalline resin composition for camera module>
The above components are melt kneaded at a cylinder temperature of 350 ° C. using a twin-screw extruder (TEX30α type, manufactured by Nippon Steel Works) at the ratio shown in Table 1 or Table 2, and a liquid crystalline resin composition for a camera module. Pellets were obtained.

<Melt viscosity>
The melt viscosity of the liquid crystalline resin compositions for camera modules of Examples and Comparative Examples was measured using the pellets. Specifically, the apparent melt viscosity under conditions of a cylinder temperature of 350 ° C. and a shear rate of 1000 sec ⁻¹ was measured based on ISO 11443 using a capillary rheometer (Capillograph 1D manufactured by Toyo Seiki: piston diameter 10 mm). For the measurement, an orifice having an inner diameter of 1 mm and a length of 20 mm was used. The results are shown in Tables 1 and 2.

<Load deflection temperature>
The pellets of Examples and Comparative Examples were molded under the following molding conditions using a molding machine (“SE100DU” manufactured by Sumitomo Heavy Industries, Ltd.) to obtain test specimens (4 mm × 10 mm × 80 mm). . Using this test piece, the deflection temperature under load was measured by a method in accordance with ISO 75-1,2. Note that 1.8 MPa was used as the bending stress. The results are shown in Tables 1 and 2.
〔Molding condition〕
Cylinder temperature: 350 ° C
Mold temperature: 80 ℃
Back pressure: 2.0MPa
Injection speed: 33mm / sec

<Bending test>
The pellets of Examples and Comparative Examples were molded under the following molding conditions using a molding machine (“SE100DU” manufactured by Sumitomo Heavy Industries, Ltd.) to produce a bending test piece of 130 mm × 13 mm × 0.8 mm. . Using this test piece, bending strength, bending elastic modulus, and breaking strain were measured in accordance with ASTM D790. The results are shown in Tables 1 and 2.
〔Molding condition〕
Cylinder temperature: 350 ° C
Mold temperature: 90 ℃
Injection speed: 33mm / sec
Holding pressure: 50 MPa

<Charpy impact test>
The pellets of Examples and Comparative Examples were molded into test specimens (4 mm × 10 mm × 80 mm) under the following molding conditions using a molding machine (“SE100DU” manufactured by Sumitomo Heavy Industries, Ltd.). Using this test piece, Charpy impact strength was measured by a method based on ISO 179-1. The results are shown in Tables 1 and 2.
〔Molding condition〕
Cylinder temperature: 350 ° C
Mold temperature: 80 ℃
Back pressure: 2.0MPa
Injection speed: 33mm / sec

<Flatness>
The pellets of Examples and Comparative Examples were molded under the following molding conditions using a molding machine (“SE-100DU” manufactured by Sumitomo Heavy Industries, Ltd.), and 5 flat plate test pieces of 80 mm × 80 mm × 1 mm were formed. A sheet was produced. The first flat plate test piece was left on a horizontal plane, and a CNC image measuring machine (model: QVBHU404-PRO1F) manufactured by Mitutoyo Co., Ltd. was used at nine locations on the flat plate test piece from the horizontal plane. The height was measured, and the average height was calculated from the obtained measurement values. The position where the height was measured is that each vertex of this square is placed on a principal plane of a flat specimen when a square with a side of 74 mm is placed so that the distance from each side of the principal plane is 3 mm. , A position corresponding to the midpoint of each side of the square and the intersection of two diagonal lines of the square. The height from the horizontal plane was the same as the average height, and a plane parallel to the horizontal plane was used as a reference plane. The maximum height and the minimum height from the reference plane were selected from the heights measured at the nine locations, and the difference between the two was calculated. Similarly, the above difference was calculated for the other four flat test pieces, and the obtained five values were averaged to obtain the flatness value. The results are shown in Tables 1 and 2.
〔Molding condition〕
Cylinder temperature: 350 ° C
Mold temperature: 80 ℃
Injection speed: 33mm / sec
Holding pressure: 60 MPa

<Number of dust generation>
The pellets of Examples and Comparative Examples were molded under the following molding conditions using a molding machine (“SE30DUZ” manufactured by Sumitomo Heavy Industries, Ltd.) to obtain a molded body of 12.5 mm × 120 mm × 0.8 mm. This molded body was used as a test piece.
〔Molding condition〕
Cylinder temperature: 350 ° C
Mold temperature: 90 ℃
Injection speed: 80mm / sec
[Evaluation]
The test piece was subjected to an ultrasonic cleaner (output 300 W, frequency 45 kHz) in water at room temperature for 3 minutes. Thereafter, the number of particles of 2 μm or more present in the water was measured with a particle counter (RION Co., Ltd., fine particle counter KL-11A (PARTICLECOUNTER)) and evaluated as the number of dust generation. The results are shown in Tables 1 and 2.

  As is clear from the results shown in Tables 1 and 2, it was confirmed that the compacts produced using the pellets of the Examples had a small number of dusts even when ultrasonically cleaned. Moreover, the said molded object had a small numerical value of flatness. From these results, the molded body formed by molding the pellets of the examples is greatly different in surface condition from the molded body formed by molding normal liquid crystalline resin composition pellets such as comparative examples, and warped deformation. Can be said to be suppressed.

  Moreover, it was confirmed that the molded object manufactured using the pellet of an Example is excellent in heat resistance.

  Furthermore, it was confirmed that the molded bodies produced using the pellets of the examples have high mechanical strength such as bending strength and impact resistance. Therefore, by molding the pellets of the embodiment, the mechanical strength is high. Specifically, for example, a camera that is less likely to break due to an impact at the time of a collision with a non-contact reader or an impact of a drive. Module parts can be manufactured.

  In addition, it was confirmed that the pellets of the examples had high fluidity during melting and excellent moldability.

DESCRIPTION OF SYMBOLS 1 Camera module 10 Board | substrate 11 Optical element 12 Lead wiring 13 Lens holder 14 Barrel 15 Lens 16 IR filter 17 Guide

Claims (4)

(A) liquid crystalline resin,
(B) Fibrous wollastonite,
(C) an epoxy group-containing copolymer, and (D) a plate-like filler,
The content of the component (A) is 55 to 95.5% by mass, the content of the component (B) is 2.5 to 25% by mass, the content of the component (C) is 1.0 to 4.5% by mass, (D) The liquid crystalline resin composition for camera modules whose content of a component is 10-35 mass% and whose total content of (B) component and (D) component is 20-37.5 mass%.   2. The (C) epoxy group-containing copolymer is at least one selected from the group consisting of (C1) an epoxy group-containing olefin copolymer and (C2) an epoxy group-containing styrene copolymer. A composition according to 1.   A camera module part comprising the composition according to claim 1.   A camera module comprising the component according to claim 3.

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