JP2017132910A - Polycarbonate resin composition for optical components and optical component - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a polycarbonate resin composition that has an excellent hue and also has extremely low mold-contamination during molding, and an optical component.SOLUTION: A polycarbonate resin composition for optical components has, based on polycarbonate resin (A) 100 pts.mass, a polyalkylene glycol polymer (B) having a neopentyl ether unit of 0.05-4 pts.mass and a phosphorous stabilizer (C) of 0.005-0.5 pts.mass.SELECTED DRAWING: None

Description

  The present invention relates to a polycarbonate resin composition for optical parts and an optical part, and more particularly relates to a polycarbonate resin composition for optical parts having a good hue and extremely low mold contamination during molding, and an optical part molded therefrom. .

  A surface light source device is incorporated in a liquid crystal display device used for a personal computer, a cellular phone and the like in order to meet demands for thinning, lightening, labor saving, and high definition. The surface light source device has a wedge-shaped cross-section light guide plate or a flat plate shape with a uniform inclined surface for the purpose of uniformly and efficiently guiding incident light to the liquid crystal display side. A light guide plate is provided. In some cases, an uneven pattern is formed on the surface of the light guide plate to provide a light scattering function.

  Such a light guide plate is obtained by injection molding of a thermoplastic resin, and the above concavo-convex pattern is imparted by transferring a concavo-convex portion formed on the surface of the nest. Conventionally, the light guide plate has been molded from a resin material such as polymethylmethacrylate (PMMA). Recently, however, a display device that displays a clearer image has been demanded, and the temperature inside the device is increased by heat generated near the light source. Therefore, it is being replaced with a polycarbonate resin material having higher heat resistance.

  Polycarbonate resin is excellent in mechanical properties, thermal properties, electrical properties, and weather resistance, but its light transmittance is lower than that of PMMA, etc., so that a surface light source body is formed from a light guide plate made of polycarbonate resin and a light source. When configured, there is a problem that the luminance is low. Recently, it has been demanded to reduce the difference in chromaticity between the light incident portion of the light guide plate and a location away from the light incident portion, but there is a problem that the polycarbonate resin is more easily yellowed than the PMMA resin.

  Patent Document 1 describes a method for improving light transmittance and luminance by adding an acrylic resin and an alicyclic epoxy. Patent Document 2 describes a method for modifying the end of the polycarbonate resin to transfer the uneven portion to the light guide plate. A method for improving the brightness by increasing the brightness, and Patent Document 3 propose a method for improving the brightness by introducing a copolyester carbonate having an aliphatic segment to improve the transferability.

  However, although the method of Patent Document 1 improves the hue by adding an acrylic resin, the light transmittance and luminance cannot be increased due to white turbidity, and the transmittance is improved by adding an alicyclic epoxy. Although there is a possibility, the effect of improving the hue is not recognized. In the case of Patent Document 2 and Patent Document 3, although an improvement effect of fluidity and transferability can be expected, there is a drawback that heat resistance is lowered.

On the other hand, it is known that polyethylene glycol or the like is blended with a thermoplastic resin such as a polycarbonate resin. Patent Document 4 discloses a γ-irradiation-resistant polycarbonate resin containing the same, and Patent Document 5 blends with PMMA or the like. A thermoplastic resin composition having excellent antistatic properties and surface appearance is described.
And in patent document 6, the proposal which improves the transmittance | permeability and a hue is made | formed by mix | blending the polyalkylene glycol comprised by a linear alkyl group. By adding polytetramethylene ether glycol, the transmittance and yellowing degree (yellow index: YI) are improved.

  However, in recent years, especially in various portable terminals such as smartphones and tablet terminals, thinning and large-sized thinning are proceeding at a remarkable speed, and the edge type in which light is incident on the light guide plate from the direct edge type to the side edge. Has been adopted, and sufficient luminance as an ultra-thin light source has been required. In such a high-end light guide plate, at present, the required specifications are not satisfied at the transmittance and YI level achieved by the above-described conventional technology.

JP-A-11-158364 JP 2001-208917 A JP 2001-215336 A JP-A-1-22959 JP-A-9-227785 Japanese Patent No. 5699188

  The present invention has been made in view of the above circumstances, and its purpose is to provide a polycarbonate resin for optical components that has a good hue and extremely little mold contamination during molding without impairing the original properties of the polycarbonate resin. It is to provide a composition and an optical component.

As a result of intensive studies to achieve the above-mentioned problems, the present inventor is good by blending a polyalkylene glycol polymer having a neopentyl ether unit in a specific amount and further containing a phosphorus stabilizer. The present inventors have found that a polycarbonate resin composition for optical parts having an excellent hue and extremely little mold contamination during molding can be obtained, and the present invention has been completed.
The present invention provides the following polycarbonate resin composition for optical parts and optical parts.

[1] Polyalkylene glycol polymer (B) having a neopentyl ether unit of 0.05 to 4 parts by mass and phosphorus stabilizer (C) of 0.005 to 0.5 with respect to 100 parts by mass of the polycarbonate resin (A). A polycarbonate resin composition for optical parts, comprising a mass part.
[2] The polycarbonate resin composition for optical components according to [1], further containing 0.0005 to 0.2 parts by mass of the epoxy compound (D) with respect to 100 parts by mass of the polycarbonate resin (A).
[3] The polycarbonate resin composition for optical components according to the above [1] or [2], wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol copolymer having a neopentyl ether unit and a tetramethylene ether unit. object.
[4] The polycarbonate resin composition for optical parts according to any one of [1] to [3], wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol polymer having a dineopentyl ether unit.
[5] The optical component according to any one of [1] to [4], wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol copolymer having a dineopentyl ether unit and a tetramethylene ether unit. Polycarbonate resin composition.
[6] The polycarbonate resin composition for optical parts according to any one of the above [1] to [5], wherein the polycarbonate resin (A) has a viscosity average molecular weight (Mv) of 10,000 to 15,000.
[7] An optical component comprising the polycarbonate resin composition according to any one of [1] to [6].

  The polycarbonate resin composition for optical parts of the present invention contains a polyalkylene glycol polymer (B) having a neopentyl ether unit in combination with a phosphorus stabilizer (C), thereby suppressing the amount of deposits on the mold. As a result, the hue is greatly improved, the mold contamination is extremely small during molding, and an optical component having a good hue can be obtained without impairing the original properties of the polycarbonate resin.

In the Example of this invention, it is a schematic diagram which shows the drop type | mold metal mold | die used by evaluation of metal mold | die contamination | contamination property.

Hereinafter, the present invention will be described in detail with reference to embodiments and examples.
In the present specification, “to” is used in the sense of including the numerical values described before and after the lower and upper limits unless otherwise specified.

[Overview]
The polycarbonate resin composition for optical parts of the present invention comprises 0.05 to 4 parts by mass of a polyalkylene glycol polymer (B) having a neopentyl ether unit and a phosphorus stabilizer (100 parts by mass) with respect to 100 parts by mass of the polycarbonate resin (A). C) 0.005 to 0.5 parts by mass is contained.
Hereinafter, each component, optical component and the like constituting the polycarbonate resin composition of the present invention will be described in detail.

[Polycarbonate resin (A)]
There is no restriction | limiting in the kind of polycarbonate resin used in this invention, A polycarbonate resin may use 1 type and may use 2 or more types together by arbitrary combinations and arbitrary ratios.

The polycarbonate resin is a polymer having a basic structure having a carbonic acid bond represented by the formula: — [— O—X—O—C (═O) —] —.
In the formula, X is generally a hydrocarbon, but for imparting various properties, X into which a hetero atom or a hetero bond is introduced may be used.

  The polycarbonate resin can be classified into an aromatic polycarbonate resin in which carbon directly bonded to a carbonic acid bond is aromatic carbon and an aliphatic polycarbonate resin in which aliphatic carbon is aliphatic carbon, either of which can be used. Of these, aromatic polycarbonate resins are preferred from the viewpoints of heat resistance, mechanical properties, electrical characteristics, and the like.

  Although there is no restriction | limiting in the specific kind of polycarbonate resin, For example, the polycarbonate polymer formed by making a dihydroxy compound and a carbonate precursor react is mentioned. At this time, in addition to the dihydroxy compound and the carbonate precursor, a polyhydroxy compound or the like may be reacted. Further, a method of reacting carbon dioxide with a cyclic ether using a carbonate precursor may be used. The polycarbonate polymer may be linear or branched. Further, the polycarbonate polymer may be a homopolymer composed of one type of repeating unit or a copolymer having two or more types of repeating units. At this time, the copolymer can be selected from various copolymerization forms such as a random copolymer and a block copolymer. In general, such a polycarbonate polymer is a thermoplastic resin.

  Among monomers used as raw materials for aromatic polycarbonate resins, examples of aromatic dihydroxy compounds include:

Dihydroxybenzenes such as 1,2-dihydroxybenzene, 1,3-dihydroxybenzene (ie, resorcinol), 1,4-dihydroxybenzene;
Dihydroxybiphenyls such as 2,5-dihydroxybiphenyl, 2,2′-dihydroxybiphenyl, 4,4′-dihydroxybiphenyl;

2,2′-dihydroxy-1,1′-binaphthyl, 1,2-dihydroxynaphthalene, 1,3-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 1,6-dihydroxynaphthalene, 2,6-dihydroxynaphthalene, , 7-dihydroxynaphthalene, dihydroxynaphthalene such as 2,7-dihydroxynaphthalene;

2,2′-dihydroxydiphenyl ether, 3,3′-dihydroxydiphenyl ether, 4,4′-dihydroxydiphenyl ether, 4,4′-dihydroxy-3,3′-dimethyldiphenyl ether, 1,4-bis (3-hydroxyphenoxy) Dihydroxy diaryl ethers such as benzene and 1,3-bis (4-hydroxyphenoxy) benzene;

2,2-bis (4-hydroxyphenyl) propane (ie, bisphenol A),
1,1-bis (4-hydroxyphenyl) propane,
2,2-bis (3-methyl-4-hydroxyphenyl) propane,
2,2-bis (3-methoxy-4-hydroxyphenyl) propane,
2- (4-hydroxyphenyl) -2- (3-methoxy-4-hydroxyphenyl) propane,
1,1-bis (3-tert-butyl-4-hydroxyphenyl) propane,
2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane,
2,2-bis (3-cyclohexyl-4-hydroxyphenyl) propane,
2- (4-hydroxyphenyl) -2- (3-cyclohexyl-4-hydroxyphenyl) propane,
α, α′-bis (4-hydroxyphenyl) -1,4-diisopropylbenzene,
1,3-bis [2- (4-hydroxyphenyl) -2-propyl] benzene,
Bis (4-hydroxyphenyl) methane,
Bis (4-hydroxyphenyl) cyclohexylmethane,
Bis (4-hydroxyphenyl) phenylmethane,
Bis (4-hydroxyphenyl) (4-propenylphenyl) methane,
Bis (4-hydroxyphenyl) diphenylmethane,
Bis (4-hydroxyphenyl) naphthylmethane,
1,1-bis (4-hydroxyphenyl) ethane,
1,1-bis (4-hydroxyphenyl) -1-phenylethane,
1,1-bis (4-hydroxyphenyl) -1-naphthylethane,
1,1-bis (4-hydroxyphenyl) butane,
2,2-bis (4-hydroxyphenyl) butane,
2,2-bis (4-hydroxyphenyl) pentane,
1,1-bis (4-hydroxyphenyl) hexane,
2,2-bis (4-hydroxyphenyl) hexane,
1,1-bis (4-hydroxyphenyl) octane,
2,2-bis (4-hydroxyphenyl) octane,
4,4-bis (4-hydroxyphenyl) heptane,
2,2-bis (4-hydroxyphenyl) nonane,
1,1-bis (4-hydroxyphenyl) decane,
1,1-bis (4-hydroxyphenyl) dodecane,
Bis (hydroxyaryl) alkanes such as;

1,1-bis (4-hydroxyphenyl) cyclopentane,
1,1-bis (4-hydroxyphenyl) cyclohexane,
1,1-bis (4-hydroxyphenyl) -3,3-dimethylcyclohexane,
1,1-bis (4-hydroxyphenyl) -3,4-dimethylcyclohexane,
1,1-bis (4-hydroxyphenyl) -3,5-dimethylcyclohexane,
1,1-bis (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane,
1,1-bis (4-hydroxy-3,5-dimethylphenyl) -3,3,5-trimethylcyclohexane,
1,1-bis (4-hydroxyphenyl) -3-propyl-5-methylcyclohexane,
1,1-bis (4-hydroxyphenyl) -3-tert-butyl-cyclohexane,
1,1-bis (4-hydroxyphenyl) -4-tert-butyl-cyclohexane,
1,1-bis (4-hydroxyphenyl) -3-phenylcyclohexane,
1,1-bis (4-hydroxyphenyl) -4-phenylcyclohexane,
Bis (hydroxyaryl) cycloalkanes such as;

9,9-bis (4-hydroxyphenyl) fluorene,
Cardio structure-containing bisphenols such as 9,9-bis (4-hydroxy-3-methylphenyl) fluorene;

4,4′-dihydroxydiphenyl sulfide,
Dihydroxydiaryl sulfides such as 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfide;

Dihydroxydiaryl sulfoxides such as 4,4'-dihydroxydiphenyl sulfoxide, 4,4'-dihydroxy-3,3'-dimethyldiphenyl sulfoxide;

4,4′-dihydroxydiphenyl sulfone,
Dihydroxydiaryl sulfones such as 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfone;
Etc.

Among these, bis (hydroxyaryl) alkanes are preferable, and bis (4-hydroxyphenyl) alkanes are particularly preferable, and 2,2-bis (4-hydroxyphenyl) propane (especially from the viewpoint of impact resistance and heat resistance). That is, bisphenol A) is preferred.
In addition, 1 type may be used for an aromatic dihydroxy compound and it may use 2 or more types together by arbitrary combinations and a ratio.

In addition, when an example of a monomer that is a raw material of the aliphatic polycarbonate resin is given,
Ethane-1,2-diol, propane-1,2-diol, propane-1,3-diol, 2,2-dimethylpropane-1,3-diol, 2-methyl-2-propylpropane-1,3- Alkanediols such as diol, butane-1,4-diol, pentane-1,5-diol, hexane-1,6-diol, decane-1,10-diol;

Cyclopentane-1,2-diol, cyclohexane-1,2-diol, cyclohexane-1,4-diol, 1,4-cyclohexanedimethanol, 4- (2-hydroxyethyl) cyclohexanol, 2,2,4, Cycloalkanediols such as 4-tetramethyl-cyclobutane-1,3-diol;

Glycols such as ethylene glycol, 2,2'-oxydiethanol (ie, diethylene glycol), triethylene glycol, propylene glycol, spiro glycol and the like;

1,2-benzenedimethanol, 1,3-benzenedimethanol, 1,4-benzenedimethanol, 1,4-benzenediethanol, 1,3-bis (2-hydroxyethoxy) benzene, 1,4-bis ( 2-hydroxyethoxy) benzene, 2,3-bis (hydroxymethyl) naphthalene, 1,6-bis (hydroxyethoxy) naphthalene, 4,4′-biphenyldimethanol, 4,4′-biphenyldiethanol, 1,4- Aralkyl diols such as bis (2-hydroxyethoxy) biphenyl, bisphenol A bis (2-hydroxyethyl) ether, bisphenol S bis (2-hydroxyethyl) ether;

1,2-epoxyethane (ie ethylene oxide), 1,2-epoxypropane (ie propylene oxide), 1,2-epoxycyclopentane, 1,2-epoxycyclohexane, 1,4-epoxycyclohexane, 1-methyl And cyclic ethers such as -1,2-epoxycyclohexane, 2,3-epoxynorbornane, and 1,3-epoxypropane;

  Among the monomers used as the raw material for the polycarbonate resin, carbonyl halides, carbonate esters and the like are used as examples of the carbonate precursor. In addition, 1 type may be used for a carbonate precursor and it may use 2 or more types together by arbitrary combinations and a ratio.

  Specific examples of carbonyl halides include phosgene; haloformates such as bischloroformate of dihydroxy compounds and monochloroformate of dihydroxy compounds.

  Specific examples of the carbonate ester include diaryl carbonates such as diphenyl carbonate and ditolyl carbonate; dialkyl carbonates such as dimethyl carbonate and diethyl carbonate; biscarbonate bodies of dihydroxy compounds, monocarbonate bodies of dihydroxy compounds, and cyclic carbonates. And carbonate bodies of dihydroxy compounds such as

Manufacturing method of polycarbonate resin The manufacturing method of polycarbonate resin is not specifically limited, Arbitrary methods are employable. Examples thereof include an interfacial polymerization method, a melt transesterification method, a pyridine method, a ring-opening polymerization method of a cyclic carbonate compound, and a solid phase transesterification method of a prepolymer.
Hereinafter, a particularly preferable one of these methods will be described in detail.

Interfacial Polymerization Method First, a case where a polycarbonate resin is produced by an interfacial polymerization method will be described.
In the interfacial polymerization method, a dihydroxy compound and a carbonate precursor (preferably phosgene) are reacted in the presence of an organic solvent inert to the reaction and an aqueous alkaline solution, usually at a pH of 9 or higher. Polycarbonate resin is obtained by interfacial polymerization in the presence. In the reaction system, a molecular weight adjusting agent (terminal terminator) may be present as necessary, or an antioxidant may be present to prevent the oxidation of the dihydroxy compound.

  The dihydroxy compound and the carbonate precursor are as described above. Of the carbonate precursors, phosgene is preferably used, and a method using phosgene is particularly called a phosgene method.

  Examples of the organic solvent inert to the reaction include chlorinated hydrocarbons such as dichloromethane, 1,2-dichloroethane, chloroform, monochlorobenzene and dichlorobenzene; aromatic hydrocarbons such as benzene, toluene and xylene; It is done. In addition, 1 type may be used for an organic solvent and it may use 2 or more types together by arbitrary combinations and a ratio.

  Examples of the alkali compound contained in the alkaline aqueous solution include alkali metal compounds and alkaline earth metal compounds such as sodium hydroxide, potassium hydroxide, lithium hydroxide, and sodium hydrogen carbonate, among which sodium hydroxide and water Potassium oxide is preferred. In addition, 1 type may be used for an alkali compound and it may use 2 or more types together by arbitrary combinations and a ratio.

  Although there is no restriction | limiting in the density | concentration of the alkali compound in alkaline aqueous solution, Usually, in order to control pH in the alkaline aqueous solution of reaction to 10-12, it is used at 5-10 mass%. For example, when phosgene is blown, the molar ratio of the bisphenol compound and the alkali compound is usually 1: 1.9 or more in order to control the pH of the aqueous phase to be 10 to 12, preferably 10 to 11. Among these, it is preferable that the ratio is 1: 2.0 or more, usually 1: 3.2 or less, and more preferably 1: 2.5 or less.

  Examples of the polymerization catalyst include aliphatic tertiary amines such as trimethylamine, triethylamine, tributylamine, tripropylamine, and trihexylamine; alicyclic rings such as N, N′-dimethylcyclohexylamine and N, N′-diethylcyclohexylamine. Formula tertiary amines; aromatic tertiary amines such as N, N′-dimethylaniline and N, N′-diethylaniline; quaternary ammonium salts such as trimethylbenzylammonium chloride, tetramethylammonium chloride, triethylbenzylammonium chloride, etc. Pyridine or a salt thereof; and the like. In addition, 1 type may be used for a polymerization catalyst and it may use 2 or more types together by arbitrary combinations and a ratio.

  Examples of the molecular weight regulator include aromatic phenols having a monohydric phenolic hydroxyl group; aliphatic alcohols such as methanol and butanol; mercaptans; phthalimides and the like. Of these, aromatic phenols are preferred. Specific examples of such aromatic phenols include alkyl groups such as m-methylphenol, p-methylphenol, m-propylphenol, p-propylphenol, p-tert-butylphenol, and p-long chain alkyl-substituted phenol. Examples thereof include substituted phenols; vinyl group-containing phenols such as isopropanyl phenol; epoxy group-containing phenols; carboxyl group-containing phenols such as o-hydroxybenzoic acid and 2-methyl-6-hydroxyphenylacetic acid; In addition, a molecular weight regulator may use 1 type and may use 2 or more types together by arbitrary combinations and a ratio.

  The usage-amount of a molecular weight regulator is 0.5 mol or more normally with respect to 100 mol of dihydroxy compounds, Preferably it is 1 mol or more, and is 50 mol or less normally, Preferably it is 30 mol or less. By making the usage-amount of a molecular weight modifier into this range, the thermal stability and hydrolysis resistance of a resin composition can be improved.

In the reaction, the order of mixing the reaction substrate, reaction medium, catalyst, additive and the like is arbitrary as long as a desired polycarbonate resin is obtained, and an appropriate order may be arbitrarily set. For example, when phosgene is used as the carbonate precursor, the molecular weight regulator can be mixed at any time as long as it is between the reaction (phosgenation) of the dihydroxy compound and phosgene and the start of the polymerization reaction.
In addition, reaction temperature is 0-40 degreeC normally, and reaction time is normally several minutes (for example, 10 minutes)-several hours (for example, 6 hours).

Next, a case where a polycarbonate resin is produced by a melt transesterification method will be described.
In the melt transesterification method, for example, a transesterification reaction between a carbonic acid diester and a dihydroxy compound is performed.

The dihydroxy compound is as described above.
On the other hand, examples of the carbonic acid diester include dialkyl carbonate compounds such as dimethyl carbonate, diethyl carbonate, and di-tert-butyl carbonate; diphenyl carbonate; substituted diphenyl carbonate such as ditolyl carbonate, and the like. Among these, diphenyl carbonate and substituted diphenyl carbonate are preferable, and diphenyl carbonate is more preferable. In addition, carbonic acid diester may use 1 type and may use 2 or more types together by arbitrary combinations and a ratio.

  The ratio of the dihydroxy compound and the carbonic acid diester is arbitrary as long as the desired polycarbonate resin is obtained, but it is preferable to use an equimolar amount or more of the carbonic acid diester with respect to 1 mol of the dihydroxy compound, and above all, 1.01 mol or more is used. It is more preferable. The upper limit is usually 1.30 mol or less. By setting it as such a range, the amount of terminal hydroxyl groups can be adjusted to a suitable range.

  In the polycarbonate resin, the amount of terminal hydroxyl groups tends to have a great influence on thermal stability, hydrolysis stability, color tone and the like. For this reason, you may adjust the amount of terminal hydroxyl groups as needed by a well-known arbitrary method. In the transesterification reaction, a polycarbonate resin in which the amount of terminal hydroxyl groups is adjusted can be usually obtained by adjusting the mixing ratio of the carbonic diester and the aromatic dihydroxy compound; the degree of vacuum during the transesterification reaction, and the like. In addition, the molecular weight of the polycarbonate resin usually obtained can also be adjusted by this operation.

When adjusting the amount of terminal hydroxyl groups by adjusting the mixing ratio of the carbonic acid diester and the dihydroxy compound, the mixing ratio is as described above.
Further, as a more aggressive adjustment method, there may be mentioned a method in which a terminal terminator is mixed separately during the reaction. Examples of the terminal terminator at this time include monohydric phenols, monovalent carboxylic acids, carbonic acid diesters, and the like. In addition, 1 type may be used for a terminal terminator and it may use 2 or more types together by arbitrary combinations and a ratio.

  When producing a polycarbonate resin by the melt transesterification method, a transesterification catalyst is usually used. Any transesterification catalyst can be used. Among them, it is preferable to use, for example, an alkali metal compound and / or an alkaline earth metal compound. In addition, auxiliary compounds such as basic boron compounds, basic phosphorus compounds, basic ammonium compounds, and amine compounds may be used in combination. In addition, 1 type may be used for a transesterification catalyst and it may use 2 or more types together by arbitrary combinations and a ratio.

  In the melt transesterification method, the reaction temperature is usually 100 to 320 ° C. The pressure during the reaction is usually a reduced pressure condition of 2 mmHg or less. As a specific operation, a melt polycondensation reaction may be performed under the above-mentioned conditions while removing a by-product such as an aromatic hydroxy compound.

  The melt polycondensation reaction can be performed by either a batch method or a continuous method. When performing by a batch type, the order which mixes a reaction substrate, a reaction medium, a catalyst, an additive, etc. is arbitrary as long as a desired aromatic polycarbonate resin is obtained, What is necessary is just to set an appropriate order arbitrarily. However, considering the stability of the polycarbonate resin and the like, the melt polycondensation reaction is preferably carried out continuously.

  In the melt transesterification method, a catalyst deactivator may be used as necessary. As the catalyst deactivator, a compound that neutralizes the transesterification catalyst can be arbitrarily used. Examples thereof include sulfur-containing acidic compounds and derivatives thereof. In addition, 1 type may be used for a catalyst deactivator and it may use 2 or more types together by arbitrary combinations and a ratio.

  The amount of the catalyst deactivator used is usually 0.5 equivalents or more, preferably 1 equivalent or more, and usually 10 equivalents or less, relative to the alkali metal or alkaline earth metal contained in the transesterification catalyst. Preferably it is 5 equivalents or less. Furthermore, it is 1 ppm or more normally with respect to polycarbonate resin, and is 100 ppm or less normally, Preferably it is 20 ppm or less.

The molecular weight of the polycarbonate resin (A) is preferably 10,000 to 15,000 in terms of viscosity average molecular weight (Mv) converted from the solution viscosity measured at a temperature of 25 ° C. using methylene chloride as a solvent. Preferably it is 10,500 or more, More preferably, it is 11,000 or more, Especially, 11,500 or more, Most preferably, it is 12,000 or more, More preferably, it is 14,500 or less. By making the viscosity average molecular weight more than the lower limit of the above range, the mechanical strength of the polycarbonate resin composition of the present invention can be further improved, and by making the viscosity average molecular weight not more than the upper limit of the above range, The fluidity of the polycarbonate resin composition of the invention can be suppressed and improved, and the molding processability can be improved and the thin-wall molding process can be easily performed.
Two or more types of polycarbonate resins having different viscosity average molecular weights may be mixed and used, and in this case, a polycarbonate resin having a viscosity average molecular weight outside the above-mentioned preferred range may be mixed.

The viscosity average molecular weight [Mv] is obtained by using methylene chloride as a solvent and obtaining an intrinsic viscosity [η] (unit: dl / g) at a temperature of 20 ° C. using an Ubbelohde viscometer. , Η = 1.23 × 10 ⁻⁴ Mv ^0.83 . The intrinsic viscosity [η] is a value calculated from the following equation by measuring the specific viscosity [η _sp ] at each solution concentration [C] (g / dl).

  The terminal hydroxyl group concentration of the polycarbonate resin is arbitrary and may be appropriately selected and determined, but is usually 1000 ppm or less, preferably 800 ppm or less, more preferably 600 ppm or less. Thereby, the residence heat stability and color tone of polycarbonate resin can be improved more. In addition, the lower limit is usually 10 ppm or more, preferably 30 ppm or more, more preferably 40 ppm or more, particularly for polycarbonate resins produced by the melt transesterification method. Thereby, the fall of molecular weight can be suppressed and the mechanical characteristic of a resin composition can be improved more.

  In addition, the unit of a terminal hydroxyl group density | concentration represents the mass of the terminal hydroxyl group with respect to the mass of polycarbonate resin in ppm. The measurement method is colorimetric determination (method described in Macromol. Chem. 88 215 (1965)) by the titanium tetrachloride / acetic acid method.

  The polycarbonate resin is a polycarbonate resin alone (the polycarbonate resin alone is not limited to an embodiment containing only one type of polycarbonate resin, and is used in a sense including an embodiment containing a plurality of types of polycarbonate resins having different monomer compositions and molecular weights, for example. .), Or an alloy (mixture) of a polycarbonate resin and another thermoplastic resin may be used in combination. Further, for example, for the purpose of further improving flame retardancy and impact resistance, a polycarbonate resin is copolymerized with an oligomer or polymer having a siloxane structure; for the purpose of further improving thermal oxidation stability and flame retardancy A monomer, oligomer or polymer having a copolymer; a monomer, oligomer or polymer having a dihydroxyanthraquinone structure for the purpose of improving thermal oxidation stability; A copolymer with an oligomer or polymer having an olefin structure; a copolymer with a polyester resin oligomer or polymer for the purpose of improving chemical resistance; Good.

  Further, in order to improve the appearance of the molded product and improve the fluidity, the polycarbonate resin may contain a polycarbonate oligomer. The viscosity average molecular weight [Mv] of this polycarbonate oligomer is usually 1500 or more, preferably 2000 or more, and is usually 9500 or less, preferably 9000 or less. Furthermore, the polycarbonate ligomer contained is preferably 30% by mass or less of the polycarbonate resin (including the polycarbonate oligomer).

Further, the polycarbonate resin may be not only a virgin raw material but also a polycarbonate resin regenerated from a used product (so-called material-recycled polycarbonate resin).
However, the regenerated polycarbonate resin is preferably 80% by mass or less of the polycarbonate resin, and more preferably 50% by mass or less. Recycled polycarbonate resin is likely to have undergone deterioration such as heat deterioration and aging deterioration, so when such polycarbonate resin is used more than the above range, hue and mechanical properties can be reduced. It is because there is sex.

[Polyalkylene glycol polymer (B)]
The polycarbonate resin composition for optical components of the present invention contains a polyalkylene glycol polymer (B) having a neopentyl ether unit.
The neopentyl ether unit is an ether-containing unit represented by the following formula (1) derived from neopentyl glycol, that is, (2,2-diethyl) trimethylene glycol.
_{- [- CH 2 -C (CH} 3) 2 CH 2 O -] - ... (1)
The neopentyl ether unit is preferably a dineopentyl ether unit, and is an ether-containing unit represented by the following formula (2) derived from dineopentyl glycol.
_{- [- CH 2 -C (CH} 3) 2 CH 2 O-CH 2 -C (CH 3) 2 CH 2 O -] - ... (2)
In the following description, the ether-containing unit derived from dineopentyl glycol of the above formula (2) is calculated as a molar amount twice as much as 1 mol of neopentyl ether unit of the formula (1).

  The polyalkylene glycol polymer (B) having a neopentyl ether unit may be a homopolymer composed of neopentyl ether units represented by the above formulas (1) and (2), and has other alkylene ether units. A copolymer may also be used. Examples of other alkylene ether units other than those represented by formulas (1) and (2) include linear or side chain units.

  As a linear alkylene ether unit, when this is mentioned as alkylene glycol, ethylene glycol, trimethylene glycol, tetramethylene glycol, pentamethylene glycol and hexamethylene glycol are preferable, and tetramethylene glycol is more preferable.

Moreover, as a branched alkylene ether unit, if it mentions as alkylene glycol, ethylene glycol which has branches, such as (2-methyl) ethylene glycol, (2-ethyl) ethylene glycol, (2,2-dimethyl) ethylene glycol;
(2-methyl) trimethylene glycol, (3-methyl) trimethylene glycol, (2-ethyl) trimethylene glycol, (3-ethyl) triethylene glycol, (2,2-dimethyl) trimethylene glycol, (2, 2-Methyleneethyl) trimethylene glycol, (3,3-dimethyl) trimethylene glycol, (3,3-methylethyl) trimethylene glycol, (3,3-diethyl) trimethylene glycol and other trimethylene glycols having branches Kind;

  (3-methyl) tetramethylene glycol, (4-methyl) tetramethylene glycol, (3-ethyl) tetramethylene glycol, (4-ethyl) tetramethylene glycol, (3,3-dimethyl) tetramethylene glycol, (3 3-methylethyl) tetramethylene glycol, (3,3-diethyl) tetramethylene glycol, (4,4-dimethyl) tetramethylene glycol, (4,4-methylethyl) tetramethylene glycol, (4,4-diethyl) Tetramethylene glycols having branches such as tetramethylene glycol;

  (3-methyl) pentamethylene glycol, (4-methyl) pentamethylene glycol, (5-methyl) pentamethylene glycol, (3-ethyl) pentamethylene glycol, (4-ethyl) pentamethylene glycol, (5-ethyl) Pentamethylene glycol, (3,3-dimethyl) pentamethylene glycol, (3,3-methylethyl) pentamethylene glycol, (3,3-diethyl) pentamethylene glycol, (4,4-dimethyl) pentamethylene glycol, ( 4,4-methylethyl) pentamethylene glycol, (4,4-diethyl) pentamethylene glycol, (5,5-dimethyl) pentamethylene glycol, (5,5-methylethyl) pentamethylene glycol, (5,5- Diethyl) pentamethylene glycol, etc. Such as pentamethylene glycol having a branching thereof.

  As mentioned above, although the alkylene ether unit was described as glycol for convenience, it should be understood that not only these glycols but also these alkylene oxides or these polyether-forming derivatives are described in the same manner.

  When the polyalkylene glycol polymer (B) is a copolymer with other alkylene ether units other than those represented by formulas (1) and (2), the other alkylene ether units may be one kind or two or more kinds of copolymers. The copolymer may be a random copolymer or a block copolymer.

The amount of neopentyl ether units is preferably 10 mol% or more in terms of mol%, more preferably 15 mol% or more, still more preferably 20 mol% or more, particularly preferably 25 mol% or more, and preferably 80 mol% or more. It is less than mol%, more preferably less than 70 mol%, still more preferably less than 60 mol%, and particularly preferably less than 50 mol%.
When the amount of the neopentyl ether unit is less than 10 mol%, the polyalkylene glycol polymer (B) tends to be decomposed and the amount of deposits on the mold tends to increase. Compatibility with (A) tends to decrease.
Further, the amount of the dineopentyl ether unit is preferably 5 mol% or more, more preferably 10 mol% or more, and still more preferably calculated as 2 mol of neopentyl ether unit as described above. It is 15 mol% or more, preferably less than 60 mol%, more preferably less than 50 mol%, and particularly preferably less than 40 mol%, particularly preferably 30 mol% or less.
The molar fraction can be measured by various methods, but is preferably measured using a ¹ H-NMR measuring apparatus and deuterated chloroform as a solvent.

  As a method for producing a polyalkylene glycol polymer having a neopentyl ether unit, a known method can be applied, and the above-described glycol, alkylene oxide or a polyether-forming derivative thereof is usually reacted with an acid catalyst. It can be produced by condensation.

  In the polyalkylene glycol polymer (B), the terminal group is preferably a hydroxyl group. In addition, even if one end or both ends are blocked with alkyl ether, aryl ether, aralkyl ether, fatty acid ester, aryl ester or the like, there is no effect on the performance, and etherified products or esterified products can be used similarly.

  As the alkyl group constituting the terminal alkyl ether, either linear or branched, alkyl groups having 1 to 22 carbon atoms such as methyl group, ethyl group, propyl group, butyl group, octyl group, lauryl group can be used. And stearyl group, and preferred examples include polyalkylene glycol methyl ether, ethyl ether, butyl ether, lauryl ether, stearyl ether and the like.

  The aryl group constituting the terminal aryl ether is preferably an aryl group having 6 to 22 carbon atoms, more preferably 6 to 12 carbon atoms, still more preferably 6 to 10 carbon atoms, such as a phenyl group, a tolyl group, or a naphthyl group. A phenyl group, a tolyl group and the like are preferable. The aralkyl group is preferably an aralkyl group having 7 to 23 carbon atoms, more preferably 7 to 13 carbon atoms, still more preferably 7 to 11 carbon atoms, and examples thereof include a benzyl group and a phenethyl group. Particularly preferred.

The fatty acid constituting the terminal fatty acid ester may be linear or branched, and may be a saturated fatty acid or an unsaturated fatty acid.
The fatty acid constituting the terminal fatty acid ester is a monovalent or divalent fatty acid having 1 to 22 carbon atoms, for example, a monovalent saturated fatty acid, such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, enanthate. Acid, caprylic acid, capric acid, lauric acid, myristic acid, pentadecylic acid, palmitic acid, heptadecylic acid, stearic acid, nonadecanoic acid, arachidic acid, behenic acid and monounsaturated fatty acids such as oleic acid, elaidic acid Unsaturated fatty acids such as linoleic acid, linolenic acid, and arachidonic acid, and divalent fatty acids having 10 or more carbon atoms, such as sebacic acid, undecanedioic acid, dodecanedioic acid, tetradecanedioic acid, tapsiaic acid and decenedioic acid, Undecenedioic acid, dodecenedioic acid.

  The aryl group constituting the terminal aryl ester is preferably an aryl group having 6 to 22 carbon atoms, more preferably 6 to 12 carbon atoms, still more preferably 6 to 10 carbon atoms, such as a phenyl group, a tolyl group, or a naphthyl group. A phenyl group, a tolyl group and the like are preferable. Since the end-capping group exhibits good compatibility with polycarbonate even if it is an aralkyl group, it can exhibit the same action as an aryl group. The aralkyl group preferably has 7 to 23 carbon atoms, more preferably Aralkyl groups having 7 to 13 carbon atoms, more preferably 7 to 11 carbon atoms are preferable, and examples thereof include benzyl group and phenethyl group, and benzyl group is particularly preferable.

The number average molecular weight of the polyalkylene glycol polymer (B) is preferably 200 to 5,000, more preferably 300 or more, further preferably 500 or more, more preferably 4,000 or less, still more preferably. Is 3,000 or less. Exceeding the upper limit of the above range is not preferable because the compatibility tends to decrease, and if it is lower than the lower limit of the above range, gas is likely to be generated during molding, which is not preferable.
The number average molecular weight of a polyalkylene glycol copolymer here is a number average molecular weight calculated based on the hydroxyl value measured based on JISK1577.

The polyalkylene glycol polymer (B) is particularly preferably a polyalkylene glycol copolymer having a neopentyl ether unit and a tetramethylene ether unit, and the neopentyl ether unit is 10 mol% or more and less than 90 mol%, tetra The methylene ether unit is preferably more than 10 mol% and 90 mol% or less, more preferably the neopentyl ether unit is 15 mol% or more, and the tetramethylene ether unit is less than 80 mol%, particularly less than 70 mol%, especially 60 mol. % Or less is preferable.
The polyalkylene glycol polymer (B) is also particularly preferably a copolymer comprising a dineopentyl ether unit and a tetramethylene ether unit. At this time, the dineopentyl ether unit is preferably 5 mol% or more, more preferably 10 mol% or more, and even more preferably 15 mol, as calculated as 2 mol of the neopentyl ether unit as described above. It is at least mol%, preferably less than 60 mol%, more preferably less than 50 mol%, particularly preferably less than 40 mol%, particularly preferably not more than 30 mol%.

As such a polyalkylene glycol polymer (B), specifically, for example, “Polyserine DCB” manufactured by NOF Corporation (hereinafter the same), “PTG-L” manufactured by Hodogaya Chemical Co., Ltd., manufactured by Asahi Kasei Corporation “PTXG” and the like can be mentioned.
Moreover, the copolymer which consists of a tetramethylene ether unit and a 2, 2- dimethyl trimethylene ether unit can also be manufactured by the method as described in Japanese Patent Application No. 2015-2533.

  Content of a polyalkylene glycol polymer (B) is 0.05-4 mass parts with respect to 100 mass parts of polycarbonate resin (A). Preferable content is 0.1 parts by mass or more, more preferable content is 0.15 parts by mass or more, more preferably 0.2 parts by mass or more, preferably 3.5 parts by mass or less, more preferably 3 parts by mass. Hereinafter, it is further preferably 2.5 parts by mass or less, particularly preferably 2 parts by mass or less. When the content is less than 0.05 parts by mass, the hue and yellowing are not sufficiently improved. When the content exceeds 4 parts by mass, the transmittance decreases due to white turbidity of the polycarbonate resin, and at the time of melt kneading by an extruder. The strand breaks frequently, making it difficult to produce resin composition pellets.

[Phosphorus stabilizer (C)]
The polycarbonate resin composition of the present invention needs to contain a phosphorus stabilizer. By containing a phosphorus stabilizer, the hue of the polycarbonate resin composition of the present invention is improved, and the heat discoloration is further improved.
Any known phosphorous stabilizer can be used. Specific examples include phosphorus oxo acids such as phosphoric acid, phosphonic acid, phosphorous acid, phosphinic acid, and polyphosphoric acid; acidic pyrophosphate metal salts such as acidic sodium pyrophosphate, acidic potassium pyrophosphate, and acidic calcium pyrophosphate; phosphoric acid Phosphates of Group 1 or Group 2B metals such as potassium, sodium phosphate, cesium phosphate, and zinc phosphate; phosphate compounds, phosphite compounds, phosphonite compounds and the like are mentioned, and phosphite compounds are particularly preferred. By selecting a phosphite compound, a polycarbonate resin composition having higher discoloration resistance and continuous productivity can be obtained.

Here, the phosphite compound is a trivalent phosphorus compound represented by the general formula: P (OR) ₃ , and R represents a monovalent or divalent organic group.
Examples of such phosphite compounds include triphenyl phosphite, tris (monononylphenyl) phosphite, tris (monononyl / dinonyl phenyl) phosphite, tris (2,4-di-tert-butylphenyl) phosphine. Phyto, monooctyl diphenyl phosphite, dioctyl monophenyl phosphite, monodecyl diphenyl phosphite, didecyl monophenyl phosphite, tridecyl phosphite, trilauryl phosphite, tristearyl phosphite, distearyl pentaerythritol diphosphite, Bis (2,4-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite, bis (2,6-di-tert-butylphenyl) octyl phosphite, 2,2-methyle Bis (4,6-di-tert-butylphenyl) octyl phosphite, tetrakis (2,4-di-tert-butylphenyl) -4,4′-biphenylene-diphosphite, 2,4,8,10-tetra- and tert-butyl-6- [3- (3-tert-butyl-hydroxy-5-methylphenyl) propoxy] dibenzo [d, f] [1,3,2] -dioxaphosphine.

  Among such phosphite compounds, an aromatic phosphite compound represented by the following formula (a) or (b) is more preferable because the heat discoloration resistance of the polycarbonate resin composition of the present invention is effectively increased. .

In the formula (a), R ¹ , R ² and R ³ may be the same or different and each represents an aryl group having 6 to 30 carbon atoms.

In formula (b), R ⁴ and R ⁵ may be the same or different and each represents an aryl group having 6 to 30 carbon atoms.

  As the phosphite compound represented by the above formula (a), triphenyl phosphite, tris (monononylphenyl) phosphite, tris (2,4-di-tert-butylphenyl) phosphite and the like are preferable. Of these, tris (2,4-di-tert-butylphenyl) phosphite is more preferable. Specific examples of such organic phosphite compounds include “ADEKA STAB 1178” manufactured by ADEKA, “SUMILIZER TNP” manufactured by Sumitomo Chemical Co., Ltd., “JP-351” manufactured by Johoku Chemical Industry Co., Ltd., and “ADEKA STAB manufactured by ADEKA. 2112 "," Irgaphos 168 "manufactured by BASF," JP-650 "manufactured by Johoku Chemical Industry Co., Ltd., and the like.

  Examples of the phosphite compound represented by the above formula (b) include bis (2,4-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite and bis (2,6-di-tert- Those having a pentaerythritol diphosphite structure such as butyl-4-methylphenyl) pentaerythritol diphosphite and bis (2,4-dicumylphenyl) pentaerythritol diphosphite are particularly preferred. Specific examples of such an organic phosphite compound include “Adeka Stub PEP-24G”, “Adeka Stub PEP-36” manufactured by Adeka Corporation, “Doverphos S-9228” manufactured by Doverchemical, and the like.

Among the phosphite compounds, the aromatic phosphite compound represented by the above formula (b) is more preferable because the hue is more excellent.
In addition, 1 type may contain phosphorus stabilizer and 2 or more types may contain it by arbitrary combinations and a ratio.

  Content of phosphorus stabilizer (C) is 0.005-0.5 mass part with respect to 100 mass parts of polycarbonate resin (A), Preferably it is 0.007 mass part or more, More preferably, it is 0.00. 008 parts by mass or more, particularly preferably 0.01 parts by mass or more, preferably 0.4 parts by mass or less, more preferably 0.3 parts by mass or less, still more preferably 0.2 parts by mass or less, particularly 0.1 parts by mass or less. When the content of the phosphorus stabilizer (C) is less than 0.005 parts by mass of the above range, the hue and heat discoloration are insufficient, and the content of the phosphorus stabilizer (C) is 0.5 parts by mass. If it exceeds 1, not only the heat discoloration is deteriorated, but also the wet heat stability is lowered.

[Epoxy compound (D)]
It is also preferable that the resin composition of the present invention contains an epoxy compound (D). By including the epoxy compound (D) together with the polyalkylene glycol polymer (B), the heat discoloration can be further improved.

As the epoxy compound (D), a compound having one or more epoxy groups in one molecule is used. Specifically, phenyl glycidyl ether, allyl glycidyl ether, t-butylphenyl glycidyl ether, 3,4-epoxycyclohexylmethyl-3 ′, 4′-epoxycyclohexylcarboxylate, 3,4-epoxy-6-methylcyclohexylmethyl -3 ', 4'-epoxy-6'-methylcyclohexyl carboxylate, 2,3-epoxycyclohexylmethyl-3', 4'-epoxycyclohexyl carboxylate, 4- (3,4-epoxy-5-methylcyclohexyl) Butyl-3 ′, 4′-epoxycyclohexylcarboxylate, 3,4-epoxycyclohexylethylene oxide, cyclohexylmethyl 3,4-epoxycyclohexylcarboxylate, 3,4-epoxy-6-methylcyclohexylmethyl-6 ′ -Methylsiloxyl carboxylate, bisphenol-A diglycidyl ether, tetrabromobisphenol-A glycidyl ether, diglycidyl ester of phthalic acid, diglycidyl ester of hexahydrophthalic acid, bis-epoxy dicyclopentadienyl ether, bis- Epoxyethylene glycol, bis-epoxycyclohexyl adipate, butadiene diepoxide, tetraphenylethylene epoxide, octyl epoxytalate, epoxidized polybutadiene, 3,4-dimethyl-1,2-epoxycyclohexane, 3,5-dimethyl-1,2, -Epoxycyclohexane, 3-methyl-5-t-butyl-1,2-epoxycyclohexane, octadecyl-2,2-dimethyl-3,4-epoxycyclohexylcarboxy N-butyl-2,2-dimethyl-3,4-epoxycyclohexyl carboxylate, cyclohexyl-2-methyl-3,4-epoxycyclohexyl carboxylate, n-butyl-2-isopropyl-3,4-epoxy -5-methylcyclohexyl carboxylate, octadecyl-3,4-epoxycyclohexylcarboxylate, 2-ethylhexyl-3 ', 4'-epoxycyclohexylcarboxylate, 4,6-dimethyl-2,3-epoxycyclohexyl-3', 4′-epoxycyclohexylcarboxylate, 4,5-epoxytetrahydrophthalic anhydride, 3-tert-butyl-4,5-epoxytetrahydrophthalic anhydride, diethyl 4,5-epoxy-cis-1,2-cyclohexyldicarboxylate Rate, j-n-b Le -3-t-butyl-4,5-epoxy - cis-1,2-cyclohexyl dicarboxylate, epoxidized soybean oil, can be preferably exemplified such as epoxidized linseed oil.
Epoxy compounds may be used alone or in combination of two or more.

  Of these, alicyclic epoxy compounds are preferably used, and 3,4-epoxycyclohexylmethyl-3 ', 4'-epoxycyclohexylcarboxylate is particularly preferable.

  The content of the epoxy compound (D) is preferably 0.0005 to 0.2 parts by mass, more preferably 0.001 parts by mass or more, and still more preferably 0 with respect to 100 parts by mass of the polycarbonate resin (A). 0.003 parts by mass or more, particularly preferably 0.005 parts by mass or more, more preferably 0.15 parts by mass or less, still more preferably 0.1 parts by mass or less, particularly preferably 0.05 parts by mass or less. . When the content of the epoxy compound (D) is less than 0.0005 parts by mass, the hue and the heat discoloration tend to be insufficient, and when it exceeds 0.2 parts by mass, the heat discoloration is not only deteriorated. Also, hue and wet heat stability are likely to decrease.

[Additives, etc.]
The polycarbonate resin composition of the present invention includes other additives other than those described above, for example, antioxidants, mold release agents, ultraviolet absorbers, fluorescent brighteners, pigments, dyes, other polymers other than polycarbonate resins, Additives such as a flame retardant, an impact resistance improver, an antistatic agent, a plasticizer, and a compatibilizing agent can be contained. These additives may be used alone or in combination of two or more.

[Production Method of Polycarbonate Resin Composition]
There is no restriction | limiting in the manufacturing method of the polycarbonate resin composition of this invention, The manufacturing method of a well-known polycarbonate resin composition can be employ | adopted widely, polycarbonate resin (A), polyalkylene glycol polymer (B), and phosphorus stabilizer (C ), And other components to be blended as needed, for example, using various mixers such as a tumbler and a Henschel mixer, then, Banbury mixer, roll, Brabender, single screw kneading extruder, twin screw kneading Examples of the method include melt kneading using a mixer such as an extruder or a kneader. The temperature for melt kneading is not particularly limited, but is usually in the range of 240 to 320 ° C.

[Optical parts]
The polycarbonate resin composition for optical components of the present invention can be produced by molding pellets obtained by pelletizing the above-described polycarbonate resin composition by various molding methods. Moreover, the resin melt-kneaded by an extruder can be directly molded into an optical component without going through the pellets.

Since the polycarbonate resin composition of the present invention is excellent in transmittance and hue and reduces mold contamination during molding, an optical component, particularly a thin optical component that is prone to mold contamination is molded by injection molding. It is used suitably for. The resin temperature at the time of injection molding is preferably molded at a resin temperature higher than 260 to 300 ° C., which is a temperature generally applied to injection molding of polycarbonate resin, and a resin temperature of 305 to 380 ° C. is preferable. The resin temperature is preferably 310 ° C. or higher, more preferably 315 ° C. or higher, particularly preferably 320 ° C. or higher, and more preferably 370 ° C. or lower. When the conventional polycarbonate resin composition is used, there is a problem that white spot foreign matter tends to be generated on the surface of the molded product if the resin temperature at the time of molding is increased in order to mold a thin molded product. By using the resin composition of the present invention, it is possible to produce a thin molded article having a good appearance even in the above temperature range.
The resin temperature is grasped as the barrel set temperature when it is difficult to directly measure the resin temperature.

  Here, the thin molded article refers to a molded article having a plate-like portion having a thickness of usually 1 mm or less, preferably 0.8 mm or less, more preferably 0.6 mm or less. Here, the plate-like portion may be a flat plate or a curved plate, may be a flat surface, may have irregularities on the surface, and the cross section has an inclined surface. Or a wedge-shaped cross section.

Examples of optical components include components of equipment and instruments that directly or indirectly use light sources such as LEDs, organic EL, incandescent bulbs, fluorescent lamps, and cathode tubes, and light guide plates and surface light emitter members are typical. It is illustrated as a thing.
The light guide plate is used to guide light from a light source such as an LED in a liquid crystal backlight unit, various display devices, and lighting devices. It diffuses by the unevenness and emits uniform light. The shape is usually flat, and the surface may or may not have irregularities.
The light guide plate is usually formed preferably by an injection molding method, an ultra-high speed injection molding method, an injection compression molding method, or the like.
The light guide plate molded using the resin composition of the present invention has a good hue, little molding failure due to mold contamination, no white turbidity or a decrease in transmittance, and a very good transmittance and hue.

  The light guide plate made of the polycarbonate resin composition of the present invention can be suitably used in the fields of liquid crystal backlight units, various display devices, and lighting devices. Examples of such devices include mobile phones, mobile notebooks, netbooks, slate PCs, tablet PCs, smartphones, tablet terminals, and other portable terminals, cameras, watches, notebook computers, various displays, lighting devices, and the like. It is done.

Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not construed as being limited to the following examples.
The raw materials and evaluation methods used in the following examples and comparative examples are as follows. In addition, the measuring method of the viscosity average molecular weight of polycarbonate resin (A) is as having mentioned above.

(Examples 1-8, Comparative Examples 1-5)
[Production of resin composition pellets]
Each component described above was blended in the proportions (parts by mass) shown in Table 2 below, mixed for 20 minutes with a tumbler, and then a single screw extruder with a vent with a screw diameter of 40 mm (“VS-” manufactured by Tanabe Plastic Machinery Co., Ltd.). 40 ”), the mixture was melt-kneaded at a cylinder temperature of 240 ° C., and pellets were obtained by strand cutting.

[Measurement of Hue (YI)]
The obtained pellets were dried at 120 ° C. for 5 to 7 hours with a hot air circulating dryer, and then with an injection molding machine (“EC100SX-2A” manufactured by Toshiba Machine Co., Ltd.) at a resin temperature of 340 ° C. and a mold temperature of 80 ° C. A long optical path molded product (300 mm × 7 mm × 4 mm) was molded.
About this long optical path molded product, YI (yellowing degree) was measured at an optical path length of 300 mm. For the measurement, a long optical path spectral transmission color meter (“ASA 1” manufactured by Nippon Denshoku Industries Co., Ltd., C light source, 2 ° visual field) was used.

[Evaluation of mold contamination (mold deposits)]
(I) Evaluation of contamination in injection molding (mold contamination)
After the pellets obtained above were dried at 120 ° C. for 5 hours, an injection molding machine (“MINIMAT M8 / 7A” manufactured by Sumitomo Heavy Industries, Ltd.) was used, and a drop mold as shown in FIG. 1 was used. Then, 200 shot injection molding was performed under conditions of a cylinder temperature of 340 ° C., a molding cycle of 10 seconds, and a mold temperature of 40 ° C., and the state of dirt due to white deposits generated on the metal mirror surface on the mold fixing side after completion was The following criteria compared with Comparative Example 3 were evaluated and judged visually.
A: Mold deposits are much less than the state after 200 shot molding of Comparative Example 3, and the mold contamination resistance is very good.
B: Although mold deposits are less than the state after 200-shot molding in Comparative Example 3, mold contamination resistance is slightly observed.
C: Although mold deposits are less than the state after 200 shot molding of Comparative Example 3, mold contamination is clearly seen.
D: Mold adhering material is at the same level as that after the 200-shot molding in Comparative Example 3, and the mold contamination is noticeable.

The drop mold shown in FIG. 1 is a mold designed to introduce a resin composition from the gate G so that the generated gas easily accumulates at the tip P portion. The gate G has a width of 1 mm and a thickness of 1 mm. In FIG. 1, the width h1 is 14.5 mm, the length h2 is 7 mm, the length h3 is 27 mm, and the thickness of the molded part is 3 mm.
The above evaluation results are shown in Table 2 below.

As is apparent from Table 2, the molded product of the example has a small YI at 300 mm with a long optical path length, and shows little yellowing. In addition, it can be seen that the amount of deposits on the mold is small.
On the other hand, in Comparative Examples 1, 4 and 5, it can be seen that 300 mmYI is higher than that of the Example. Moreover, it turns out that the comparative examples 2 and 3 have much mold deposit amount compared with an Example.
Therefore, it can be seen that the object of the present invention to provide a polycarbonate resin composition for optical parts having a good hue and no adhesion to a mold is achieved only when all the requirements of the present invention are satisfied.

  The polycarbonate resin composition of the present invention has a good hue, has very little mold contamination, and does not have white turbidity or a decrease in transmittance. Therefore, it can be used suitably for optical parts, and has very high industrial applicability. high.

Claims (7)

  0.05 to 4 parts by mass of a polyalkylene glycol polymer (B) having a neopentyl ether unit and 0.005 to 0.5 parts by mass of a phosphorus stabilizer (C) with respect to 100 parts by mass of the polycarbonate resin (A). A polycarbonate resin composition for optical parts, comprising:   Furthermore, the polycarbonate resin composition for optical components of Claim 1 which contains an epoxy compound (D) 0.0005-0.2 mass part with respect to 100 mass parts of polycarbonate resin (A).   The polycarbonate resin composition for optical parts according to claim 1 or 2, wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol copolymer having a neopentyl ether unit and a tetramethylene ether unit.   The polycarbonate resin composition for optical parts according to any one of claims 1 to 3, wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol polymer having a dineopentyl ether unit.   The polycarbonate resin composition for an optical component according to any one of claims 1 to 4, wherein the polyalkylene glycol polymer (B) is a polyalkylene glycol copolymer having a dineopentyl ether unit and a tetramethylene ether unit. object.   The polycarbonate resin composition for optical parts according to any one of claims 1 to 5, wherein the polycarbonate resin (A) has a viscosity average molecular weight (Mv) of 10,000 to 15,000.   The optical component which consists of a polycarbonate resin composition of any one of Claims 1-6.