JP2017014530A - Polycarbonate resin composition and manufacturing method therefor - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a polycarbonate resin composition excellent in surface hardness, heat resistance moldability, color tone and impact resistance.SOLUTION: There is provided a polycarbonate resin composition containing at least a polycarbonate resin (a) and a polycarbonate resin (b) having different structural unit from the polycarbonate resin (a) and satisfying following conditions. (i) pencil hardness defined in ISO 15184 of the polycarbonate resin (a) is higher than pencil hardness defined in ISO 15184 of the polycarbonate resin (b). (ii) weight ratio between the polycarbonate (a) and the polycarbonate (b) in the polycarbonate resin composition is in a range of 1:99 to 45:55. (iii) melt viscosity of the polycarbonate resin (b) at temperature of 280°C and shear rate of 122 secis higher than melt viscosity of the polycarbonate resin (a) at temperature of 280°C and shear rate of 122 sec.SELECTED DRAWING: None

Description

  The present invention relates to a polycarbonate resin composition and a method for producing the same. More specifically, the present invention relates to a polycarbonate resin composition containing at least two types of polycarbonate resins having different structural units and a method for producing the same.

  Polycarbonate resins are excellent in mechanical strength, electrical properties, transparency, and the like, and are widely used as engineering plastics in various fields such as the electrical / electronic equipment field and the automotive field. In recent years, in these fields of application, thinner, smaller, and lighter molded products have been developed, and further improvements in the performance of molding materials are required. However, the conventional polycarbonate resin using bisphenol A as a raw material has not been sufficiently excellent in surface hardness. Therefore, it has been desired to develop a polycarbonate resin having a high surface hardness, and several proposals have been made.

  For example, Patent Document 1 and Patent Document 2 propose a method for producing a polycarbonate / copolycarbonate having excellent surface hardness using a bisphenol different from bisphenol A as a monomer.

  Further, Patent Document 3 proposes a method in which different types of polymers are pasted on a molded piece such as a hard coat treatment to form a multilayer structure.

  Patent Document 4 proposes to improve the surface hardness with a blended material of a polycarbonate resin derived from dimethylbisphenolcyclohexane and a bisphenol A type polycarbonate resin.

Japanese Unexamined Patent Publication No. 64-69625 JP-A-8-6183852 JP 2010-188719 A International Publication No. 2009/083933 Pamphlet

However, the material obtained by the conventional method could not obtain a polycarbonate resin polycarbonate resin composition that is thin, high in strength, excellent in heat resistance and moldability, high in surface hardness, and excellent in color tone.
Under such circumstances, an object of the present invention is to provide a polycarbonate resin composition that is particularly excellent in surface hardness and excellent in heat resistance, moldability (fluidity), color tone, and impact resistance.

  As a result of intensive studies to solve the above problems, the present inventors have found that a polycarbonate resin composition containing two specific types of polycarbonate resins can be a polycarbonate resin composition meeting the above purpose. The present invention has been reached. Specifically, a polycarbonate resin composition comprising a polycarbonate resin (a) having a relatively high pencil hardness and a specific melt viscosity, and a polycarbonate resin (b), wherein the polycarbonate resin (a) and the polycarbonate resin By making the polycarbonate resin (b) a specific weight ratio, an excellent polycarbonate resin composition having excellent surface hardness, good color tone, impact resistance and moldability comparable to conventional polycarbonate resins is obtained. I found out that

The gist of the present invention resides in the following <1> to <12>.
That is, the present invention first relates to the following polycarbonate resin composition invention.
<1> A polycarbonate resin composition comprising at least a polycarbonate resin (a) and a polycarbonate resin (b) having a structural unit different from the polycarbonate resin (a),
A polycarbonate resin composition that satisfies the following conditions.
(I) The pencil hardness specified by ISO 15184 of the polycarbonate resin (a) is higher than the pencil hardness specified by ISO 15184 of the polycarbonate resin (b) (ii) the polycarbonate resin (a) in the polycarbonate resin composition; The weight ratio with respect to the polycarbonate resin (b) is in the range of 1:99 to 45:55 (iii) The melt viscosity of the polycarbonate resin (b) at a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ is the polycarbonate resin (a ) At a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ <2> The polycarbonate resin composition according to <1>, wherein the polycarbonate resin (a) has a pencil hardness defined by ISO 15184 of F or higher. object.
<3> The polycarbonate resin composition according to <1> or <2>, wherein the pencil hardness defined by ISO 15184 of the polycarbonate resin composition is HB or more.
<4> The polycarbonate resin according to any one of <1> to <3>, wherein the polycarbonate resin (a) is a polycarbonate resin containing at least a structural unit derived from a compound represented by the following general formula (1). Composition.
(In General Formula (1), R ₁ and R ₂ each independently represent a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms or a substituted or unsubstituted aryl group, and R ₃ and R 2 ₄ each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group, and X represents a single bond, a carbonyl group, a substituted or unsubstituted group. An alkylidene group, a substituted or unsubstituted sulfur atom, or an oxygen atom.)
<5> The <4>, wherein the polycarbonate resin (a) is a polycarbonate resin containing at least a structural unit derived from at least one compound selected from the group consisting of the following general formulas (1a) to (1c). Polycarbonate resin composition.


<6> The polycarbonate resin according to any one of <1> to <5>, wherein the polycarbonate resin (b) is a polycarbonate resin mainly including a structural unit derived from a compound represented by the following general formula (2). Composition.
<7> The polycarbonate resin composition according to any one of <1> to <6>, wherein YI of the polycarbonate resin composition is 4.0 or less.

Next, this invention concerns on invention of the manufacturing method of the following polycarbonate resin compositions.
<8> In the method for producing a polycarbonate resin composition according to any one of <1> to <7>, the polycarbonate resin (a) and the polycarbonate resin (b) are melt-kneaded. A method for producing a polycarbonate resin composition.
<9> The method for producing a polycarbonate resin composition according to any one of <1> to <7>, wherein the polycarbonate resin (a) and the polycarbonate resin (b) are dry blended. A method for producing a polycarbonate resin composition.

Furthermore, this invention concerns on invention of the molded article obtained using the following polycarbonate resin compositions.
<10> An injection molded product obtained by injection molding the polycarbonate resin composition according to any one of <1> to <7>.
<11> An extruded product obtained by extrusion molding the polycarbonate resin composition according to any one of <1> to <7>.
<12> The extruded product according to <11>, wherein the extruded product is a sheet or a film.

  According to the present invention, a polycarbonate resin composition can be obtained in which the surface hardness is greatly improved, the color tone is good, and the impact resistance and moldability are balanced. That is, by making a polycarbonate resin composition containing a polycarbonate resin (b) and a polycarbonate resin (a) having a relatively high pencil hardness and a specific melt viscosity in a specific weight ratio, the polycarbonate resin (b) Without impairing the physical properties, it is possible to increase the surface hardness, maintain a good color tone, and balance impact resistance and moldability. For example, when a bisphenol A type polycarbonate is used for the polycarbonate resin (b), it is a disadvantage of the bisphenol A type polycarbonate while minimizing the reduction in impact resistance, transparency, color tone, etc., which are the characteristics of the bisphenol A type polycarbonate. The surface hardness can be improved.

The present invention is a polycarbonate resin composition comprising at least a polycarbonate resin (a) and a polycarbonate resin (b) having a structural unit different from that of the polycarbonate resin (a). The present invention relates to a polycarbonate resin composition characterized by satisfying the condition (iii).
In the present invention, “having different structural units” means
[I] When each of the polycarbonate resin (a) and the polycarbonate resin (b) is a homopolymer, it means “different types of structural units”
[II] When at least one of the polycarbonate resin (a) and the polycarbonate resin (b) is a copolymer (copolymer),
(A) The type of structural unit is different,
Or (B) the type of the structural unit is the same and the composition ratio of the structural unit is different,
It is a concept that includes
That is, a specific example of the above [I] is a case where the polycarbonate resin (a) is a homopolymer composed of the structural unit A and the polycarbonate resin (b) is a homopolymer composed of the structural unit B.
A specific example of the above [II] (A) is a copolymer in which the polycarbonate resin (a) is composed of the structural unit A and the structural unit C, and the polycarbonate resin (b) is a copolymer composed of the structural unit B and the structural unit C. This is the case.
A specific example of the above [II] (B) is that the polycarbonate resin (a) and the polycarbonate resin (b) each comprise a structural unit A and a structural unit B. In the polycarbonate resin (a) and the polycarbonate resin (b), This is a case where the ratio between the structural unit A and the structural unit B is different.

First, as the condition (i), the pencil hardness defined by ISO 15184 of the polycarbonate resin (a) constituting the polycarbonate resin composition of the present invention is higher than the pencil hardness defined by ISO 15184 of the polycarbonate resin (b). It is essential. The pencil hardness of the polycarbonate resin or polycarbonate resin composition specified here is described in detail in the evaluation method “(1) Pencil hardness of molded product” in the examples, and the pencil hardness measured as an injection molded product. It is. Hereinafter, unless otherwise specified, in this specification, when “pencil hardness” is simply described, it means the pencil hardness of the injection-molded product.
When the pencil hardness of the polycarbonate resin (a) is the same as or lower than the pencil hardness of the polycarbonate resin (b), the pencil hardness of the polycarbonate resin composition may be lowered, and the surface of the molded body is easily damaged.
The pencil hardness specified in ISO 15184 is 2B, B, HB, F, H, 2H, 3H, 4H from the lowest rank. The preferred pencil hardness of the polycarbonate resin (a) is F or more. is there. When the pencil hardness of the polycarbonate resin (a) is less than F, the pencil hardness of the polycarbonate resin composition may not be sufficiently improved.

  Next, as the condition (ii), the weight ratio of the polycarbonate resin (a) to the polycarbonate resin (b) in the polycarbonate resin composition of the present invention is in the range of 1:99 to 45:55. Preferably it is 3: 97-45: 55, More preferably, it is 5: 95-40: 60, More preferably, it is 10: 90-30: 70. When the proportion of the polycarbonate resin (a) is too large, the color tone of the resulting polycarbonate resin composition deteriorates, and sufficient impact resistance cannot be obtained. When the proportion of the polycarbonate resin (a) is too small, a pencil is used. Hardness may be insufficient.

Further, as the condition (iii), the melt viscosity of the polycarbonate resin (b) at a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ (hereinafter sometimes simply referred to as “the melt viscosity of the polycarbonate resin (b)”) is polycarbonate. It is required to be higher than the melt viscosity of the resin (a) at a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ (hereinafter sometimes simply referred to as “the melt viscosity of the polycarbonate resin (a)”).
If this condition is not satisfied, the effect of improving the surface hardness is reduced, and the color tone may be deteriorated. In addition, melt viscosity can be measured using the capillary rheometer (made by Toyo Seiki Co., Ltd.) mentioned later in an Example.

The melt viscosity of the polycarbonate resin (a) is usually in the range of 500 to 30,000 poise, preferably 1,000 to 25,000 poise, and more preferably 1,500 to 20,000 poise.
When the melt viscosity of the polycarbonate resin (a) is too high, the effect of improving the surface hardness of the obtained polycarbonate resin composition may be reduced, and the color tone (YI) of the molded product may be increased.
Further, if the melt viscosity of the polycarbonate resin (a) is too low, the glass transition temperature (Tg) of the obtained polycarbonate resin composition may be lowered, and the heat resistance may be deteriorated, and the impact resistance of the obtained polycarbonate resin composition may be reduced. It is not preferable because the property may be lowered.

The melt viscosity of the polycarbonate resin (b) is usually in the range of 1,000 to 40,000 poise, preferably 3,000 to 30,000 poise, and more preferably 5,000 to 25,000 poise.
If the melt viscosity of the polycarbonate resin (b) is too high, the effect of improving the surface hardness of the obtained polycarbonate resin composition may be reduced, and the YI of the molded product may be increased.
Further, if the melt viscosity of the polycarbonate resin (b) is too low, the glass transition temperature (Tg) of the obtained polycarbonate resin composition may be lowered, and the heat resistance may be deteriorated, and the impact resistance of the obtained polycarbonate resin composition may be reduced. It is not preferable because the property may be lowered.

The melt viscosity at a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ of the polycarbonate resin composition of the present invention is preferably 30,000 poise or less, particularly preferably 25,000 poise or less. If the melt viscosity is 30,000 poise or more, the fluidity is greatly lowered and the moldability may be deteriorated.

Thus, the first feature of the present invention is that the polycarbonate resin composition of the present invention has a relatively low pencil hardness and a high melt viscosity, and a relatively high pencil hardness and a high melt viscosity. A polycarbonate resin composition comprising a polycarbonate resin (a) having a low viscosity at a specific weight ratio.
By adopting the above-described configuration, a polycarbonate resin composition having a high hardness even in a thin wall, a high surface hardness, a high moldability and a good color tone and impact resistance can be obtained.

  In general, the polycarbonate blend and the copolymer polycarbonate resin having the same structural unit and amount thereof often have the same physical properties, but the detailed reason is not clear at present, but the polycarbonate resin ( The surface hardness of the polycarbonate resin composition containing a) and the polycarbonate resin (b) is significantly higher than the surface hardness of the copolymer polycarbonate having the same structural units as the polycarbonate resin composition in the same weight ratio.

  The polycarbonate resin composition of the present invention preferably further satisfies the following.

  YI of the polycarbonate resin composition of the present invention is usually 4.0 or less, preferably 3.5 or less, more preferably 3.0 or less, and particularly preferably 2.5 or less. When YI is too high, the color tone is deteriorated and the design property is lacking as a molded product. In particular, in a molded product product that needs to be colored, the brightness is not sufficient, and the color may become dull.

  The Charpy impact strength value of the polycarbonate resin composition is appropriately determined depending on the form and use of the final product, but is usually 11 or more. If it is less than 11, the final product may be easily broken.

  Hereinafter, a polycarbonate resin suitable as the polycarbonate resin (a) and the polycarbonate resin (b) constituting the polycarbonate resin composition of the present invention will be described.

<Polycarbonate resin (a)>
As a polycarbonate resin (a), first, a polycarbonate resin containing at least a structural unit derived from a compound represented by the following general formula (1) is a preferred example.

(In General Formula (1), R ₁ and R ₂ each independently represent a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms or a substituted or unsubstituted aryl group, and R ₃ and R 2 ₄ each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group, and X represents a single bond, a carbonyl group, a substituted or unsubstituted group. An alkylidene group, a substituted or unsubstituted sulfur atom, or an oxygen atom.)

Here, in the general formula (1), examples of the substituted or unsubstituted alkyl group having 1 to 20 carbon atoms of R ₁ and R ₂ include, for example, a methyl group, an ethyl group, an n-propyl group, and an isopropyl group. , N-butyl group, isobutyl group, sec-butyl group, tert-butyl group, n-pentyl group, sec-pentyl group, n-hexyl group, n-heptyl group, n-octyl group and the like. Examples of the unsubstituted aryl group include a phenyl group, a benzyl group, a tolyl group, a 4-methylphenyl group, and a naphthyl group.
Examples of the substituted or unsubstituted alkyl group having 1 to 20 carbon atoms of R ₃ and R ₄ include, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec -Butyl group, tert-butyl group, n-pentyl group, sec-pentyl group, n-hexyl group, n-heptyl group, n-octyl group and the like. Examples of the substituted or unsubstituted aryl group include: A phenyl group, a benzyl group, a tolyl group, 4-methylphenyl group, a naphthyl group, etc. are mentioned.
Among these, R ₁ and R ₂ are preferably a methyl group, an ethyl group, an n-propyl group, or a 4-methylphenyl group, and particularly preferably a methyl group. R ₃ and R ₄ are preferably a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, or a 4-methylphenyl group, and particularly preferably a hydrogen atom. Here, the bonding positions of R ₁ , R ₂ , R ₃ and R ₄ in the general formula (1) are arbitrarily selected from 2-position, 3-position, 5-position and 6-position with respect to X on each phenyl ring. And preferably the 3rd and 5th positions.

In the general formula (1), when X is a substituted or unsubstituted alkylidene group, it is represented by the following structural formula. Examples of the substituted or unsubstituted sulfur atom for X include —S— and —SO ₂ —.

Here, R ₅ and R ₆ each independently represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group, and Z is substituted or unsubstituted. A substituted alkylene group having 4 to 20 carbon atoms is shown.

Examples of the substituted or unsubstituted alkyl group having 1 to 20 carbon atoms of R ₅ and R ₆ include, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec- Examples include a butyl group, a tert-butyl group, an n-pentyl group, a sec-pentyl group, an n-hexyl group, an n-heptyl group, and an n-octyl group. Examples of the substituted or unsubstituted aryl group include phenyl Group, benzyl group, tolyl group, 4-methylphenyl group, naphthyl group and the like.
Among these, R ₅ and R ₆ are preferably a methyl group, an ethyl group, an n-propyl group, or a 4-methylphenyl group, and particularly preferably a methyl group.
Z is bonded to carbon bonded to two phenyl groups in the general formula (1) to form a substituted or unsubstituted divalent carbocycle. Examples of the divalent carbocycle include a cycloalkylidene group such as a cyclopentylidene group, a cyclohexylidene group, a cycloheptylidene group, a cyclododecylidene group or an adamantylidene group (preferably having a carbon number of 4 to Examples of the substituted group include those having these methyl substituents and ethyl substituents. Among these, a cyclohexylidene group, a methyl-substituted cyclohexylidene group, and a cyclododecylidene group are preferable.

Among the polycarbonate resins (a) including at least a structural unit derived from the compound represented by the general formula (1), at least one compound selected from the group consisting of the following general formulas (1a) to (1i) A polycarbonate resin containing the derived structural unit is preferably used.

  Among the above compounds, a polycarbonate resin containing a structural unit derived from at least one compound selected from the group consisting of the general formulas (1a) to (1c) is more preferably used.

The polycarbonate resin (a) may contain a structural unit other than the structural unit derived from the compound represented by the general formula (1) as long as the performance is not impaired.
Such a structural unit is not particularly limited. Specifically, 2,2-bis (4-hydroxyphenyl) propane (hereinafter sometimes referred to as “bisphenol A”), anhydrosugar alcohol, and the like. And structural units derived from cyclic ether compounds such as alicyclic dihydroxy compounds and spiroglycols. Among these, the structural unit derived from bisphenol A is particularly preferable.

<Polycarbonate resin (b)>
Next, as the polycarbonate resin (b), a polycarbonate resin containing a structural unit derived from at least one compound selected from the group consisting of the following general formulas (2) to (13) is preferably used. A bisphenol A type polycarbonate resin mainly containing a structural unit derived from bisphenol A represented by the formula (2) is more preferably used. Here, “mainly containing structural units derived from bisphenol A” means 50% by weight or more, preferably 80% by weight or more, more preferably 90% by weight or more, among the structural units constituting the polycarbonate resin (b). Means a structural unit derived from bisphenol A.
In addition, content of the structural unit in polycarbonate resin (b) can be calculated | required by NMR method. Specifically, it is used when synthesizing a polycarbonate resin (b), which is observed when a deuterated chloroform solution of the polycarbonate resin (b) is measured by ¹ H-NMR using a nuclear magnetic resonance apparatus (NMR apparatus). The molar composition of each structural unit can be determined by the characteristic signal area intensity ratio depending on the dihydroxy compound. The weight ratio of each structural unit is obtained from the obtained molar composition and the formula amount of each structural unit.

<Production method of polycarbonate resin>
Next, the manufacturing method of the polycarbonate resin (a) and the polycarbonate resin (b) of the present invention will be described. (Hereinafter, “polycarbonate resin (a) and polycarbonate resin (b)” may be collectively referred to as “polycarbonate resin”.)
The polycarbonate resin of the present invention can be obtained by polymerization using a dihydroxy compound and a carbonyl compound. Specifically, a polycarbonate resin is obtained by reacting a dihydroxy compound and carbonyl chloride (hereinafter sometimes referred to as “CDC” or “phosgene”) at the interface between an organic phase and an aqueous phase that are not arbitrarily mixed. A polycarbonate resin is produced by transesterification of a dihydroxy compound and a carbonyl compound in a molten state in the presence of a transesterification catalyst in the presence of an interfacial polycondensation method (hereinafter sometimes referred to as “interface method”). There is a melt polycondensation method (hereinafter sometimes referred to as “melting method”).
Hereinafter, each of the interface method and the melting method will be specifically described.

<Interface method>
The polycarbonate resin of the present invention by the interfacial method is usually prepared by preparing an alkaline aqueous solution of a dihydroxy compound, performing an interfacial polycondensation reaction between the dihydroxy compound and phosgene as a condensation catalyst, for example, in the presence of an amine compound, and then neutralizing. A polycarbonate resin is obtained through water washing and drying processes. Specifically, the polycarbonate resin production process by the interfacial method includes a raw material process for preparing raw materials such as monomer components, an oligomerization process in which an oligomerization reaction is performed, a polycondensation process in which a polycondensation reaction using an oligomer is performed, A washing step for washing the reaction solution after the polycondensation reaction by alkali washing, acid washing and water washing, a polycarbonate resin isolation step for pre-concentrating the washed reaction solution and isolating the polycarbonate resin after granulation, It has at least a drying step for drying the polycarbonate resin particles. Hereinafter, each step will be described.

(Primary process)
In the primary process, the primary tank is filled with a dihydroxy compound, an aqueous solution of an alkali metal compound such as sodium hydroxide (NaOH) or an alkaline earth metal compound such as magnesium hydroxide, demineralized water (DMW), and A raw material such as an alkaline aqueous solution of a dihydroxy compound containing a reducing agent such as hydrosulfite (HS) is prepared as necessary.

(Dihydroxy compound)
Specific examples of the dihydroxy compound that is a raw material of the polycarbonate resin according to the present invention include dihydroxy compounds represented by the general formulas (1) to (13).

(Alkali metal compound or alkaline earth metal compound)
As the alkali metal compound or alkaline earth metal compound, a hydroxide is usually preferable, and examples thereof include sodium hydroxide, lithium hydroxide, potassium hydroxide, magnesium hydroxide, and calcium hydroxide. Among these, sodium hydroxide is particularly preferable.
The ratio of the alkali metal compound or alkaline earth metal compound to the dihydroxy compound is usually 1.0 to 1.5 (equivalent ratio), preferably 1.02 to 1.04 (equivalent ratio). When the ratio of the alkali metal compound or alkaline earth metal compound is excessively large or excessively small, it affects the terminal group of the carbonate oligomer obtained in the oligomerization step described later, and as a result, the polycondensation reaction tends to be abnormal. There is.

(Oligomerization process)
Next, in the oligomerization step, the alkaline aqueous solution of the dihydroxy compound and phosgene (CDC) prepared in the original preparation step are mixed in a predetermined reactor in the presence of an organic solvent such as methylene chloride (CH ₂ Cl ₂ ). A phosgenation reaction of a dihydroxy compound is performed.
Subsequently, a condensation catalyst such as triethylamine (TEA) and a chain terminator such as pt-butylphenol (pTBP) are added to the mixed solution in which the phosgenation reaction of the dihydroxy compound is performed, and the oligomerization reaction of the dihydroxy compound Is done.
Next, the oligomerization reaction liquid of the dihydroxy compound was introduced into a predetermined stationary separation tank after further oligomerization reaction, and the organic phase containing the carbonate oligomer and the aqueous phase were separated and separated. The organic phase is fed to the polycondensation process.
Here, the residence time in the oligomerization step from when the alkaline aqueous solution of the dihydroxy compound is supplied to the reactor in which the phosgenation reaction of the dihydroxy compound is performed until entering the stationary separation tank is usually 120 minutes or less, preferably 30 minutes to 60 minutes.

(phosgene)
The phosgene used in the oligomerization step is usually used in liquid or gaseous form. The preferred amount of CDC used in the oligomerization step is appropriately selected depending on the reaction conditions, particularly the reaction temperature and the concentration of the dihydroxy compound in the aqueous phase, and is not particularly limited. Usually, the amount of CDC is 1 mol to 2 mol, preferably 1.05 mol to 1.5 mol, per 1 mol of the dihydroxy compound. When the amount of CDC used is excessively large, unreacted CDC increases and the basic unit tends to be extremely deteriorated. On the other hand, if the amount of CDC used is excessively small, the amount of chloroformate group is insufficient and proper molecular weight elongation tends not to be performed.

(Organic solvent)
In the oligomerization step, an organic solvent is usually used. As the organic solvent, reaction products such as phosgene and carbonate oligomers and polycarbonate resins are dissolved at the reaction temperature and reaction pressure in the oligomerization step and are not compatible with water (or do not form a solution with water). An active organic solvent is mentioned.
Examples of such inert organic solvents include aliphatic hydrocarbons such as hexane and n-heptane; chlorinations such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, trichloroethane, tetrachloroethane, dichloropropane, and 1,2-dichloroethylene. Aliphatic hydrocarbons; aromatic hydrocarbons such as benzene, toluene and xylene; chlorinated aromatic hydrocarbons such as chlorobenzene, o-dichlorobenzene and chlorotoluene; and other substituted aromatic hydrocarbons such as nitrobenzene and acetophenone It is done.
Among these, chlorinated hydrocarbons such as dichloromethane or chlorobenzene are preferably used. These inert organic solvents can be used alone or as a mixture with other solvents.

(Condensation catalyst)
The oligomerization reaction can be performed in the presence of a condensation catalyst. The addition timing of the condensation catalyst is preferably after CDC is consumed. The condensation catalyst can be arbitrarily selected from many condensation catalysts used in the two-phase interfacial condensation method. For example, trialkylamine, N-ethylpyrrolidone, N-ethylpiperidine, N-ethylmorpholine, N-isopropylpiperidine, N-isopropylmorpholine and the like can be mentioned. Of these, triethylamine and N-ethylpiperidine are preferable.

(Chain terminator)
In the present embodiment, monophenol is usually used as a chain terminator in the oligomerization step. Examples of monophenols include phenols; alkylphenols having 1 to 20 carbon atoms such as pt-butylphenol and p-cresol; halogenated phenols such as p-chlorophenol and 2,4,6-tribromophenol. Can be mentioned. The usage-amount of monophenol is suitably selected according to the molecular weight of the carbonate oligomer obtained, and is 0.5 mol%-10 mol% normally with respect to a dihydroxy compound.

In the interface method, the molecular weight of the polycarbonate resin is determined by the addition amount of a chain terminator such as monophenol. For this reason, from the viewpoint of controlling the molecular weight of the polycarbonate resin, the chain stopper is preferably added immediately after the consumption of the carbonate-forming compound is completed and before the molecular weight elongation starts.
When monophenol is added in the presence of a carbonate-forming compound, a large amount of condensates (diphenyl carbonates) of monophenols are produced, and it is difficult to obtain a polycarbonate resin having a target molecular weight. When the addition time of monophenol is extremely delayed, it becomes difficult to control the molecular weight, and furthermore, the resin has a specific shoulder on the low molecular weight side of the molecular weight distribution, and there is a tendency that problems such as dripping occur during molding.

(Branching agent)
In the oligomerization step, any branching agent can be used. Examples of such a branching agent include 2,4-bis (4-hydroxyphenylisopropyl) phenol, 2,6-bis (2-hydroxy-5-methylbenzyl) -4-methylphenol, 2- (4- Hydroxyphenyl) -2- (2,4-dihydroxyphenyl) propane, 1,4-bis (4,4′-dihydroxytriphenylmethyl) benzene and the like. In addition, 2,4-dihydroxybenzoic acid, trimesic acid, cyanuric chloride and the like can also be used. Among these, a branching agent having at least three phenolic hydroxyl groups is preferable.
The amount of branching agent used is appropriately selected according to the degree of branching of the carbonate oligomer obtained, and is usually 0.05 mol% to 2 mol% with respect to the dihydroxy compound.

In the oligomerization step, when the two-phase interfacial condensation method is employed, the organic phase containing the dihydroxy compound and the alkali metal compound or alkaline earth are contacted prior to the contact between the aqueous solution of the alkali metal compound or alkaline earth metal compound of the dihydroxy compound and phosgene. It is particularly preferred that an aqueous phase containing a metal group compound is brought into contact with an organic phase that is not arbitrarily mixed with water to form an emulsion.
Examples of means for forming such an emulsion include a stirrer having a predetermined stirring blade, a homogenizer, a homomixer, a colloid mill, a flow jet mixer, a dynamic mixer such as an ultrasonic emulsifier, a static mixer, and the like. It is preferable to use a mixer. The emulsion usually has a droplet diameter of 0.01 μm to 10 μm and has emulsion stability.
The emulsion state of the emulsion is usually represented by the Weber number or P / q (load power value per unit volume). The Weber number is preferably 10,000 or more, more preferably 20,000 or more, and most preferably 35,000 or more. Also, the upper limit is about 1,000,000 or less. P / q is preferably 200 kg · m / L or more, more preferably 500 kg · m / L or more, and most preferably 1,000 kg · m / L or more.

  The contact between the emulsion and the CDC is preferably carried out under a mixing condition that is weaker than the emulsification conditions described above in order to suppress the dissolution of CDC in the organic phase. The Weber number is less than 10,000, preferably less than 5,000, and more preferably less than 2,000. Further, P / q is less than 200 kg · m / L, preferably less than 100 kg · m / L, and more preferably less than 50 kg · m / L. CDC contact can be achieved by introducing CDC into a tubular reactor or tank reactor.

  The reaction temperature in the oligomerization step is usually 80 ° C. or lower, preferably 60 ° C. or lower, more preferably 10 ° C. to 50 ° C. The reaction time is appropriately selected depending on the reaction temperature, and is usually 0.5 minutes to 10 hours, preferably 1 minute to 2 hours. If the reaction temperature is excessively high, side reactions cannot be controlled and the CDC basic unit tends to deteriorate. If the reaction temperature is excessively low, this is a favorable situation in terms of reaction control, but the refrigeration load increases and the cost tends to increase.

  The concentration of the carbonate oligomer in the organic phase may be in a range in which the obtained carbonate oligomer is soluble, and is specifically about 10 wt% to 40 wt%. The proportion of the organic phase is preferably a volume ratio of 0.2 to 1.0 with respect to the aqueous phase containing the aqueous alkali metal salt solution or alkaline earth metal salt solution of the dihydroxy compound.

(Polycondensation process)
Next, in the polycondensation step, the organic phase containing the carbonate oligomer separated from the aqueous phase in the stationary separation tank is transferred to an oligomer storage tank having a stirrer. A condensation catalyst such as triethylamine (TEA) is further added to the oligomer storage tank.
Subsequently, the organic phase stirred in the oligomer storage tank is introduced into a predetermined polycondensation reaction tank. Subsequently, an organic solvent such as demineralized water (DMW) or methylene chloride (CH ₂ Cl ₂ ) is added to the polycondensation reaction tank. Then, an aqueous sodium hydroxide solution is supplied and mixed with stirring to carry out a polycondensation reaction of the carbonate oligomer.

Thereafter, the polycondensation reaction liquid in the polycondensation reaction tank is successively introduced successively into a plurality of polycondensation reaction tanks, and the polycondensation reaction of the carbonate oligomer is completed.
Here, in the polycondensation step, the residence time in the polycondensation reaction tank in which the polycondensation reaction of the carbonate oligomer is continuously performed is usually 12 hours or less, preferably 0.5 to 5 hours.
As a preferred embodiment of the polycondensation step, first, an organic phase containing a carbonate oligomer and an aqueous phase are separated, and an inert organic solvent is added to the separated organic phase as necessary to adjust the concentration of the carbonate oligomer. In this case, the amount of the inert organic solvent is adjusted so that the concentration of the polycarbonate resin in the organic phase obtained by the polycondensation reaction is 5% by weight to 30% by weight. Next, an aqueous solution containing water and an alkali metal compound or an alkaline earth metal compound is newly added, and in order to further adjust the polycondensation conditions, a condensation catalyst is preferably added, and a polycondensation reaction is performed according to an interfacial polycondensation method. . The ratio of the organic phase to the aqueous phase in the polycondensation reaction is preferably about volume ratio of organic phase: aqueous phase = 1: 0.2 to 1: 1.

Examples of the alkali metal compound or alkaline earth metal compound include compounds similar to those used in the oligomerization step described above. Of these, sodium hydroxide is preferred industrially. The amount of the alkali metal compound or alkaline earth metal compound used may be more than the amount that the reaction system is always kept alkaline during the polycondensation reaction. In addition, it may be divided and added as appropriate during the polycondensation reaction.
When the amount of the alkali metal compound or alkaline earth metal compound used is excessively large, the hydrolysis reaction as a side reaction tends to proceed. Therefore, the concentration of the alkali metal compound or alkaline earth metal compound contained in the aqueous phase after the completion of the polycondensation reaction is 0.05N or more, preferably 0.05N to 0.3N.
The temperature of the polycondensation reaction in the polycondensation step is usually around room temperature. The reaction time is about 0.5 to 5 hours, preferably about 1 to 3 hours.

(Washing process)
Next, after the polycondensation reaction in the polycondensation reaction tank is completed, the polycondensation reaction solution is subjected to alkali washing with an alkali washing solution, acid washing with an acid washing solution, and water washing with washing water by a known method. In addition, the total residence time of the washing step is usually 12 hours or less, preferably 0.5 to 6 hours.

(Polycarbonate resin isolation process)
In the polycarbonate resin isolation step, first, the polycondensation reaction solution containing the polycarbonate resin washed in the washing step is prepared as a concentrated solution concentrated to a predetermined solid content concentration. The solid content concentration of the polycarbonate resin in the concentrate is usually 5% to 35% by weight, preferably 10% to 30% by weight.
Next, the concentrate is continuously supplied to a predetermined granulation tank, and stirred and mixed with demineralized water (DMW) at a predetermined temperature. And the granulation process which evaporates an organic solvent is performed, maintaining a suspended state in water, and the water slurry containing a polycarbonate resin granular material is formed.
Here, the temperature of the demineralized water (DMW) is usually 37 ° C to 67 ° C, preferably 40 ° C to 50 ° C. Moreover, the solidification temperature of polycarbonate resin by the granulation process performed in a granulation tank is 37 to 67 degreeC normally, Preferably, it is 40 to 50 degreeC.
The water slurry containing the polycarbonate resin powder continuously discharged from the granulation tank is then continuously introduced into a predetermined separator, and water is separated from the water slurry.

(Drying process)
In the drying process, in the separator, the polycarbonate resin powder from which water has been separated from the water slurry is continuously supplied to a predetermined dryer, retained for a predetermined residence time, and then continuously extracted. . Examples of the dryer include a fluidized bed dryer. A plurality of fluidized bed dryers may be connected in series to continuously perform the drying process.
Here, the dryer usually has a heating means such as a heat medium jacket, for example, with water vapor, usually 0.1 MPa-G to 1.0 MPa-G, preferably 0.2 MPa-G to 0. .6 MPa-G. Thus, the temperature of nitrogen (N ₂₎ flowing through the dryer, usually, 100 ° C. to 200 DEG ° C., preferably, it is held in 120 ° C. to 180 ° C..

<Melting method>
Next, the melting method will be described.

(Dihydroxy compound)
Specific examples of the dihydroxy compound that is a raw material of the polycarbonate resin according to the present invention include dihydroxy compounds represented by the general formulas (1) to (13).

(Carbonated diester)
Examples of the carbonic acid diester that is a raw material of the polycarbonate resin according to the present invention include compounds represented by the following general formula (14).

Here, in the general formula (14), A ′ is an optionally substituted linear, branched, or cyclic monovalent hydrocarbon group having 1 to 10 carbon atoms. Two A ′ may be the same or different from each other.
In addition, as a substituent on A ′, a halogen atom, an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a phenyl group, a phenoxy group, a vinyl group, a cyano group, and an ester group Amide group, nitro group and the like.

Specific examples of the carbonic acid diester compound include substituted diphenyl carbonates such as diphenyl carbonate and ditolyl carbonate, and dialkyl carbonates such as dimethyl carbonate, diethyl carbonate, and di-t-butyl carbonate.
Among these, diphenyl carbonate (hereinafter sometimes referred to as “DPC”) and substituted diphenyl carbonate are preferable. These carbonic acid diesters can be used alone or in admixture of two or more.

Moreover, the amount of the carbonic acid diester compound is preferably 50 mol% or less, more preferably 30 mol% or less, and may be substituted with dicarboxylic acid or dicarboxylic acid ester.
Typical dicarboxylic acids or dicarboxylic acid esters include terephthalic acid, isophthalic acid, diphenyl terephthalate, diphenyl isophthalate, and the like. When substituted with such a dicarboxylic acid or dicarboxylic acid ester, a polyester carbonate is obtained.

  In the production method of the polycarbonate resin of the present invention by the melting method, the amount of these carbonic acid diesters (including the above-mentioned substituted dicarboxylic acid or dicarboxylic acid ester; the same shall apply hereinafter) is usually based on 1 mol of the dihydroxy compound. The carbonic acid diester compound is used in a ratio of 1.01 mol to 1.30 mol, preferably 1.02 mol to 1.20 mol. If the molar ratio of the carbonic acid diester is excessively small, the transesterification rate decreases, making it difficult to produce a polycarbonate resin having a desired molecular weight, or increasing the terminal hydroxyl group concentration of the resulting polycarbonate resin, resulting in thermal stability. Tend to get worse. In addition, if the molar ratio of the carbonic acid diester is excessively large, the reaction rate of the transesterification decreases, and it becomes difficult to produce a polycarbonate resin having a desired molecular weight, and the residual amount of the carbonic acid diester compound in the resin. Is unfavorable because it may cause odor when being molded or formed into a molded product.

(Transesterification catalyst)
The transesterification catalyst used in the production method of the polycarbonate resin of the present invention by a melting method is not particularly limited, and may be a catalyst usually used for producing a polycarbonate resin by the transesterification method.
In general, for example, basic compounds such as alkali metal compounds, alkaline earth metal compounds, beryllium compounds, magnesium compounds, basic boron compounds, basic phosphorus compounds, basic ammonium compounds, and amine compounds can be used. Among these, alkali metal compounds and alkaline earth metal compounds are preferable for practical use. These transesterification catalysts may be used alone or in combination of two or more.

The amount of the transesterification catalyst used is usually in the range of 1 × 10 ⁻⁹ mol to 1 × 10 ⁻³ mol with respect to 1 mol of all dihydroxy compounds, in order to obtain a polycarbonate resin excellent in molding characteristics and hue. In the case of using an alkali metal compound and / or an alkaline earth metal compound, the amount of the transesterification catalyst is preferably 1.0 × 10 ⁻⁸ mol to 1 × 10 ^{−4 with} respect to 1 mol of the total dihydroxy compound. Within a range of moles, more preferably within a range of 1.0 × 10 ⁻⁸ moles to 1 × 10 ⁻⁵ moles, particularly preferably 1.0 × 10 ⁻⁷ moles to 5.0 × 10 ⁻⁶ moles. Within range. If the amount is less than the above lower limit amount, the polymerization activity necessary for producing a polycarbonate resin having a desired molecular weight cannot be obtained. If the amount is more than the above upper limit amount, the polymer hue deteriorates, the amount of branching components is too large, and the fluidity. The polycarbonate resin having excellent target melting characteristics cannot be produced.

Examples of the alkali metal compound include inorganic alkali metal compounds such as alkali metal hydroxides, carbonates and hydrogencarbonate compounds; organic alkali metal compounds such as salts with alkali metal alcohols, phenols and organic carboxylic acids. It is done. Here, as an alkali metal, lithium, sodium, potassium, rubidium, cesium etc. are mentioned, for example.
Among these alkali metal compounds, cesium compounds are preferable, and cesium carbonate, cesium hydrogen carbonate, and cesium hydroxide are particularly preferable.

  Examples of the alkaline earth metal compound include inorganic alkaline earth metal compounds such as alkaline earth metal hydroxides and carbonates; alkaline earth metal alcohols, phenols, salts with organic carboxylic acids, and the like. It is done. Here, examples of the alkaline earth metal include calcium, strontium, barium and the like.

  Examples of the beryllium compound and magnesium compound include inorganic metal compounds such as metal hydroxides and carbonates; salts of the metals with alcohols, phenols, and organic carboxylic acids.

  Examples of basic boron compounds include sodium salts, potassium salts, lithium salts, calcium salts, magnesium salts, barium salts, strontium salts, and the like of boron compounds. Here, as the boron compound, for example, tetramethylboron, tetraethylboron, tetrapropylboron, tetrabutylboron, trimethylethylboron, trimethylbenzylboron, trimethylphenylboron, triethylmethylboron, triethylbenzylboron, triethylphenylboron, tributyl Examples include benzylboron, tributylphenylboron, tetraphenylboron, benzyltriphenylboron, methyltriphenylboron, and butyltriphenylboron.

  Examples of the basic phosphorus compound include trivalent phosphine compounds such as triethylphosphine, tri-n-propylphosphine, triisopropylphosphine, tri-n-butylphosphine, triphenylphosphine, and tributylphosphine, or derivatives thereof. And quaternary phosphonium salts.

  Examples of the basic ammonium compound include tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, trimethylethylammonium hydroxide, trimethylbenzylammonium hydroxide, trimethylphenylammonium hydroxide, Triethylmethylammonium hydroxide, triethylbenzylammonium hydroxide, triethylphenylammonium hydroxide, tributylbenzylammonium hydroxide, tributylphenylammonium hydroxide, tetraphenylammonium hydroxide, benzyltriphenylammonium hydroxide, methyltriphenylammonium hydroxide Sid, butyl triphenyl ammonium hydroxide, and the like.

  Examples of the amine compound include 4-aminopyridine, 2-aminopyridine, N, N-dimethyl-4-aminopyridine, 4-diethylaminopyridine, 2-hydroxypyridine, 2-methoxypyridine, 4-methoxypyridine, 2 -Dimethylaminoimidazole, 2-methoxyimidazole, imidazole, 2-mercaptoimidazole, 2-methylimidazole, aminoquinoline and the like.

(Catalyst deactivator)
In the present invention, a catalyst deactivator for neutralizing and deactivating the transesterification catalyst may be added after completion of the transesterification reaction. The heat resistance and hydrolysis resistance of the polycarbonate resin obtained by such treatment are improved.
As such a catalyst deactivator, an acidic compound having a pKa of 3 or less, such as sulfonic acid and sulfonic acid ester, is preferable. Specifically, benzenesulfonic acid, p-toluenesulfonic acid, methyl benzenesulfonate, benzenesulfone Examples include ethyl acetate, propyl benzenesulfonate, butyl benzenesulfonate, methyl p-toluenesulfonate, ethyl p-toluenesulfonate, propyl p-toluenesulfonate, and butyl p-toluenesulfonate.
Among these, p-toluenesulfonic acid and butyl p-toluenesulfonate are preferably used.

The method for producing a polycarbonate resin by a melting method is to prepare a raw material mixed melt of a raw material dihydroxy compound and a carbonic acid diester (original preparation step), and the raw material mixed melt is melted in the presence of a transesterification reaction catalyst. The polycondensation reaction is performed in multiple stages using a plurality of reaction tanks (polycondensation step). The reaction system may be any of a batch system, a continuous system, or a combination of a batch system and a continuous system. As the reaction tank, a plurality of vertical stirring reaction tanks and, if necessary, at least one horizontal stirring reaction tank subsequent thereto are used. Usually, these reaction tanks are installed in series and processed continuously.
After the polycondensation process, the reaction is stopped, the unreacted raw materials and reaction byproducts in the polycondensation reaction liquid are devolatilized and removed, the process of adding a thermal stabilizer, mold release agent, colorant, etc., polycarbonate resin You may add suitably the process etc. which form in a predetermined particle size.
Next, each process of the manufacturing method will be described.

(Primary process)
The dihydroxy compound and the carbonic acid diester compound used as the raw material of the polycarbonate resin are usually raw materials using a batch type, semi-batch type or continuous type stirring tank type apparatus in an atmosphere of an inert gas such as nitrogen or argon. Prepared as a mixed melt. For example, when bisphenol A is used as the dihydroxy compound and diphenyl carbonate is used as the carbonic acid diester compound, the melt mixing temperature is usually selected from the range of 120 ° C. to 180 ° C., preferably 125 ° C. to 160 ° C.
Hereinafter, a case where bisphenol A is used as a dihydroxy compound and diphenyl carbonate is used as a raw material as a carbonic acid diester compound will be described as an example.
At this time, the ratio of the dihydroxy compound and the carbonic acid diester compound is adjusted so that the carbonic acid diester compound becomes excessive. The carbonic acid diester compound is usually 1.01 mol to 1.30 mol with respect to 1 mol of the dihydroxy compound. Preferably, it is adjusted to a ratio of 1.02 mol to 1.20 mol.

(Polycondensation process)
The polycondensation by the transesterification reaction between the dihydroxy compound and the carbonic acid diester compound is usually carried out continuously in a multistage system of two or more stages, preferably 3 to 7 stages. Specific reaction conditions for each stage are temperature: 150 ° C. to 320 ° C., pressure: normal pressure to 0.01 Torr (1.3 Pa), and average residence time: 5 minutes to 150 minutes.
In each multi-stage reactor, in order to more effectively remove monohydroxy compounds such as phenol as a by-product from the system as the transesterification progresses, the reaction temperature is increased stepwise in the above reaction conditions. Set to high vacuum.

When the polycondensation step is performed in a multistage manner, usually, a plurality of reaction vessels including a vertical stirring reaction vessel are provided to increase the average molecular weight of the polycarbonate resin. The reaction tank is usually installed in 2 to 6 groups, preferably 4 to 5 groups.
Here, as a reaction tank, for example, a stirring tank type reaction tank, a thin film reaction tank, a centrifugal thin film evaporation reaction tank, a surface renewal type biaxial kneading reaction tank, a biaxial horizontal type stirring reaction tank, a wet wall reaction tank, a free tank A perforated plate type reaction vessel that polycondenses while dropping, a perforated plate type reaction vessel with wire that polycondenses while dropping along a wire, and the like are used.

  The types of stirring blades in the vertical stirring reaction tank include, for example, turbine blades, paddle blades, fiddler blades, anchor blades, full zone blades (manufactured by Shinko Environmental Solution Co., Ltd.), Sun Meller blades (manufactured by Mitsubishi Heavy Industries, Ltd.), Max blend blades (manufactured by Sumitomo Heavy Industries, Ltd.), helical ribbon blades, twisted lattice blades (manufactured by Hitachi Plant Technology Co., Ltd.), and the like.

  Moreover, a horizontal stirring reaction tank means that the rotating shaft of a stirring blade is a horizontal type (horizontal direction). As a stirring blade of a horizontal stirring reaction tank, for example, a uniaxial stirring blade such as a disk type or a paddle type, HVR, SCR, N-SCR (manufactured by Mitsubishi Heavy Industries, Ltd.), Vivolak (Sumitomo Heavy Industries, Ltd.) )), Or biaxial stirring blades such as spectacle blades and lattice blades (manufactured by Hitachi Plant Technology Co., Ltd.).

  In addition, the transesterification catalyst used for the polycondensation of a dihydroxy compound and a carbonic acid diester compound may usually be prepared as a solution in advance. The concentration of the catalyst solution is not particularly limited, and is adjusted to an arbitrary concentration according to the solubility of the catalyst in the solvent. As the solvent, acetone, alcohol, toluene, phenol, water and the like can be appropriately selected.

  When water is selected as the solvent for the catalyst, the nature of the water is not particularly limited as long as the type and concentration of impurities contained are constant, but usually distilled water or deionized water is preferably used.

<Production method of polycarbonate resin composition>
The method for producing the polycarbonate resin composition of the present invention is not particularly limited,
1) A method of melt-kneading a polycarbonate resin (a) and a polycarbonate resin (b); 2) A method of melt-kneading a molten polycarbonate resin (a) and a molten polycarbonate resin (b);
3) A method of mixing the polycarbonate resin (a) and the polycarbonate resin (b) in a solution state;
4) A method of dry blending the polycarbonate resin (a) and the polycarbonate resin (b);
Etc.
Hereinafter, each method will be described.

1) A method of melt-kneading the polycarbonate resin (a) and the polycarbonate resin (b);
The pellets or granules of the polycarbonate resin (a) and the pellets or granules of the polycarbonate resin (b) are melt kneaded using a mixing device such as a kneader, a twin screw extruder, or a single screw extruder. The pellets or granules of the polycarbonate resin (a) and the pellets or granules of the polycarbonate resin (b) may be mixed in advance in a solid state and then kneaded, or either one may be mixed with the mixing device first. It may be melted and the other polycarbonate resin added thereto and kneaded. The kneading temperature is not particularly limited, but is preferably 240 ° C or higher, more preferably 260 ° C or higher, and further preferably 280 ° C or higher.
Moreover, 350 degrees C or less is preferable and 320 degrees C or less is especially preferable. When the kneading temperature is low, the mixing of the polycarbonate resin (a) and the polycarbonate resin (b) is not complete, and there is a possibility that the hardness and impact resistance may vary when a molded product is produced, which is not preferable. Moreover, when the kneading | mixing temperature is too high, the color tone of a polycarbonate resin composition may deteriorate, and it is unpreferable.

2) A method of melt-kneading the molten polycarbonate resin (a) and the molten polycarbonate resin (b);
The molten polycarbonate resin (a) and the molten polycarbonate resin (b) are mixed using a mixing device such as a stirring tank, a static mixer, a kneader, a twin screw extruder, or a single screw extruder. At this time, for example, a polycarbonate resin obtained by a melt polymerization method may be introduced into the mixing apparatus in a molten state without being cooled and solidified. Although there is no restriction | limiting in particular as temperature to mix, 150 degreeC or more is preferable, 180 degreeC or more is more preferable, and 200 degreeC or more is preferable. Moreover, 300 degrees C or less is preferable and 250 degrees C or less is especially preferable. If the mixing temperature is low, the mixing of the polycarbonate resin (a) and the polycarbonate resin (b) is not complete, and there is a possibility that the hardness and impact resistance may vary when a molded product is produced, which is not preferable. Moreover, when the temperature to mix is too high, the color tone of a polycarbonate resin composition may deteriorate, and it is unpreferable.

3) A method of mixing the polycarbonate resin (a) and the polycarbonate resin (b) in a solution state;
In this method, the polycarbonate resin (a) and the polycarbonate resin (b) are dissolved in an appropriate solvent to form a solution, mixed in a solution state, and then isolated as a polycarbonate resin composition. Suitable solvents include, for example, aliphatic hydrocarbons such as hexane and n-heptane; chlorinated aliphatic carbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, trichloroethane, tetrachloroethane, dichloropropane and 1,2-dichloroethylene. Hydrogen; aromatic hydrocarbons such as benzene, toluene and xylene; and other substituted aromatic hydrocarbons such as nitrobenzene and acetophenone. Among these, for example, chlorinated hydrocarbons such as dichloromethane or chlorobenzene are preferably used. These solvents can be used alone or as a mixture with other solvents.
Examples of the mixing device include a stirring tank and a static mixer. Further, the mixing temperature is not particularly limited as long as the polycarbonate resin (a) and the polycarbonate resin (b) are dissolved, and the mixing temperature is usually carried out below the boiling point of the solvent used.

4) A method of dry blending the polycarbonate resin (a) and the polycarbonate resin (b);
In this method, pellets or granules of polycarbonate resin (a) and pellets or granules of polycarbonate resin (b) are dry blended using a tumbler, super mixer, Henschel mixer, Nauter mixer or the like.

Among the methods 1) to 4) above, the methods 1) and 2) in which the polycarbonate resin (a) and the polycarbonate resin (b) are melt-kneaded, and the polycarbonate resin (a) and the polycarbonate resin (b) are dry blended. The method 4) is preferred.
In producing the composition, in any of the above methods, a pigment, a dye, a release agent, a heat stabilizer and the like can be appropriately added within a range not impairing the object of the present invention.

<Production method of molded products>
In order to produce a resin molded product from the polycarbonate resin composition of the present invention, an ordinary extrusion molding machine / injection molding machine is used.

  The molding temperature is preferably 200 ° C. or higher, more preferably 250 ° C. or higher, and further preferably 280 ° C. or higher. Moreover, 350 degrees C or less is preferable and 320 degrees C or less is especially preferable. If the molding temperature is too low, the melt viscosity becomes high, the fluidity is lowered, the moldability may be lowered, the effect of improving the surface hardness is reduced, and the surface hardness of the resulting resin composition may be lowered. is there. If the molding temperature is too high, the polycarbonate resin is colored, and the color tone of the polycarbonate resin composition may be deteriorated.

<Production method of injection molded products>
In order to produce an injection molded product from the polycarbonate resin composition of the present invention, a normal injection molding machine is used.

  The mold temperature in the case of using an injection molding machine or the like is preferably 150 ° C. or lower, more preferably 120 ° C. or lower, and further preferably 100 ° C. or lower. Moreover, 30 degreeC or more is preferable and 50 degreeC or more is especially preferable. If the mold temperature is too high, it is necessary to lengthen the cooling time at the time of molding, the manufacturing cycle of the molded product becomes long, and the productivity may decrease. If the mold temperature is too low, the melt viscosity of the resin composition becomes too high, and there is a possibility that a uniform molded product may not be obtained, resulting in problems such as unevenness on the surface of the molded product.

<Manufacturing method of extruded product>
In order to produce an extruded product from the polycarbonate resin composition of the present invention, an ordinary extruder is used. In general, a T-die, a round die or the like is mounted on the extrusion molding machine, and various shapes of extrusion-molded products can be obtained. Examples of the obtained extrusion-molded product include a sheet, a film, a plate, a tube, and a pipe. Among these, a sheet or a film is preferable.

  In order to improve the adhesion, paintability, and printability of the extruded product of the polycarbonate resin composition of the present invention, a hard coat layer is laminated on both sides or one side of the extruded product, and weather resistance and / or scratch resistance is improved. The film may be heat-laminated on both sides or one side of the extrusion-molded product, or the surface may be subjected to processing such as graining, translucent and opaque processing.

  In addition, when performing injection molding or extrusion molding, pigments, dyes, mold release agents, heat stabilizers, and the like can be appropriately added as long as the object of the present invention is not impaired.

  The molded article can be used in various fields such as buildings, vehicles, electrical / electronic devices, machinery, and the like.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example, unless the summary is changed.

EXAMPLES Hereinafter, although this invention is demonstrated more concretely based on an Example, this invention is not limited to a following example.
The physical properties of the polycarbonate resin and the composition used in the examples were evaluated by the following methods.

(1) Pencil hardness of molded product Polycarbonate resin having a thickness of 3 mm, a length of 60 mm, and a width of 60 mm under the conditions of a barrel temperature of 280 ° C. and a mold temperature of 90 ° C. using an injection molding machine (J50E2 manufactured by Nippon Steel) The plate (molded product) or polycarbonate resin composition plate (molded product) was injection molded. For this molded product, the pencil hardness measured under a load of 750 g was obtained using a pencil hardness tester (manufactured by Toyo Seiki Co., Ltd.) in accordance with ISO 15184.

(2) Melt viscosity The polycarbonate resin or polycarbonate resin composition dried at 120 ° C. for 5 hours is heated to 280 ° C. using a capillary rheometer (manufactured by Toyo Seiki Co., Ltd.) having a die diameter of 1 mmφ × 30 mm and shear rate Measurement was performed at 122 (sec ⁻¹ ). If the melt viscosity is too high, the fluidity is lowered and the moldability is deteriorated, so it is necessary to keep it within an appropriate range.

(3) Viscosity average molecular weight (Mv)
A polycarbonate resin was dissolved in methylene chloride (concentration 6.0 g / L) to obtain a solution. Using this solution, the specific viscosity (ηsp) at 20 ° C. was measured with an Ubbelohde viscosity tube, and the viscosity average molecular weight (Mv) was calculated by the following formula.
ηsp / C = [η] (1 + 0.28ηsp)
[η] = 1.23 × 10 ⁻⁴ Mv ^0.83

(4) Charpy impact strength of polycarbonate resin or polycarbonate resin composition Polycarbonate resin or polycarbonate resin composition under conditions of barrel temperature of 280 ° C. and mold temperature of 90 ° C. using an injection molding machine (J50E2 manufactured by Nippon Steel Co., Ltd.) The product was molded to obtain a molded piece. The molded piece was used to measure the impact strength at a notch of 0.25 mmR based on JIS K-7111.

(5) Yellow index (YI) of polycarbonate resin or polycarbonate resin composition
The yellow index (YI) was measured with a spectrocolorimeter (CM-3700d manufactured by Minolta Co., Ltd.) using the molded product molded in (1). The smaller the value, the better the color tone.

(6) Glass transition temperature (Tg)
Using a differential operation calorimeter (DSC 6220, manufactured by SII), about 10 mg of a polycarbonate resin sample is heated at a rate of temperature increase of 20 ° C./min to measure the amount of heat. In accordance with JIS-K7121, a baseline on the low temperature side is measured. The extrapolated glass transition start temperature, which is the temperature at the intersection of the straight line extended to the high temperature side and the tangent drawn at the point where the slope of the step-like change portion of the glass transition is maximized, was determined. The extrapolated glass transition temperature was defined as the glass transition temperature (Tg).

(7) Pencil hardness of the extruded product Polycarbonate having a thickness of 240 μm and a width of 140 ± 5 mm using a 25 mmφ single-screw extruder (manufactured by Isuzu Chemical Industries Ltd.) under conditions of a barrel temperature of 280 ° C. and a roll temperature of 90 ° C. The resin or polycarbonate resin composition was extruded into a sheet (extruded product). About this extrusion molded product, the pencil hardness measured by 750g load was calculated | required using the pencil hardness tester (made by Toyo Seiki Co., Ltd.) based on ISO15184.

(8) Extruded product yellow index (YI)
The yellow index (YI) was measured with a spectrocolorimeter (CM-3700d manufactured by Minolta Co., Ltd.) using the extruded product molded in (7). The smaller the value, the better the color tone.

(9) Pencil hardness of polycarbonate resin cast product When the polycarbonate resin has a low molecular weight and a molded product for pencil hardness evaluation cannot be molded by the method described in (1) above, an evaluation sample was prepared as follows.
After adding 100 g of polycarbonate resin in a glass container with a stirring blade, nitrogen substitution was performed, and the pressure in the glass container was maintained at 101.3 kPa (760 Torr) in absolute pressure. The glass container was immersed in an oil bath heated to 280 ° C. to melt the polycarbonate resin. After the polycarbonate resin was uniformly melted, the molten polycarbonate resin was taken out from the glass container into a stainless steel bat so as to have a thickness of about 3 mm and cooled to room temperature. The cooled polycarbonate resin was measured according to ISO 15184 using a pencil hardness tester (manufactured by Toyo Seiki Co., Ltd.) under a load of 750 g.

  In addition, the polycarbonate resin used by the Example and the comparative example is as follows.

(1) Polycarbonate resin (a):
Reference Example 1 Synthesis of PC (a1) 2,2-bis (4-hydroxy-3-methylphenyl) propane (hereinafter sometimes abbreviated as “BPC”) as a raw material dihydroxy compound (Honshu Chemical Co., Ltd.) The mixture was adjusted by adding an aqueous solution of cesium carbonate to 37.60 kg (about 147 mol) and diphenyl carbonate (DPC) 32.20 kg (about 150 mol) so that the amount of cesium carbonate was 2 μmol per mol of dihydroxy compound. Next, the mixture was charged into a first reactor having an internal volume of 200 L equipped with a stirrer, a heating medium jacket, a vacuum pump, and a reflux condenser.
Next, the operation of depressurizing the inside of the first reactor to 1.33 kPa (10 Torr) and then restoring the pressure to the atmospheric pressure with nitrogen was repeated 5 times, and the inside of the first reactor was replaced with nitrogen. After nitrogen substitution, the internal temperature of the first reactor was gradually raised through a heat medium having a temperature of 230 ° C. through the heat medium jacket to dissolve the mixture. Then, the stirrer was rotated at 55 rpm, the temperature in the heat medium jacket was controlled, and the internal temperature of the 1st reactor was kept at 220 degreeC. The pressure in the first reactor was 101.3 kPa (760 Torr) in absolute pressure over 40 minutes while distilling off phenol produced as a by-product by the oligomerization reaction of BPC and DPC performed in the first reactor. To 13.3 kPa (100 Torr).
Subsequently, a transesterification reaction was performed for 80 minutes while maintaining the pressure in the first reactor at 13.3 kPa and further distilling off the phenol.
Thereafter, the inside of the system was restored to the absolute pressure of 101.3 kPa with nitrogen, the gauge pressure was increased to 0.2 MPa, and the oligomer in the first reactor was passed through a transfer pipe heated to 200 ° C. or higher in advance. Was pumped to the second reactor. The second reactor had an internal volume of 200 L, was equipped with a stirrer, a heat medium jacket, a vacuum pump and a reflux condenser, and the internal pressure was controlled to atmospheric pressure and the internal temperature was controlled to 240 ° C.
Next, the oligomer fed into the second reactor was stirred at 16 rpm, the internal temperature was raised with a heat medium jacket, and the inside of the second reactor was absolute pressure from 101.3 kPa to 13.3 kPa over 40 minutes. The pressure was reduced to. Thereafter, the temperature increase was continued, and the internal pressure was reduced from 13.3 kPa to 399 Pa (3 Torr) as an absolute pressure over an additional 40 minutes, and phenol distilled out was removed out of the system. Further, the temperature was continuously raised, and after the absolute pressure in the second reactor reached 70 Pa (about 0.5 Torr), the pressure was maintained at 70 Pa, and a polycondensation reaction was performed. The final internal temperature in the second reactor was 285 ° C. The polycondensation reaction was completed when the stirrer of the second reactor reached a predetermined stirring power.
Next, the inside of the second reactor is restored to 101.3 kPa in absolute pressure with nitrogen, and the gauge pressure is increased to 0.2 MPa, and the polycarbonate resin is extracted in a strand form from the bottom of the second reactor, The mixture was pelletized by using a rotary cutter while being cooled at the same time. The resulting polycarbonate resin had a viscosity average molecular weight of 18,500 and a melt viscosity of 2,361 Poise.

Reference Example 2 Synthesis of PC (a2) As a raw material dihydroxy compound, 1,1-bis (4-hydroxy-3-methylphenyl) cyclohexane or below may be abbreviated as “Bis-OCZ” instead of BPC. ) (Manufactured by Honshu Chemical Co., Ltd.) 43.48 kg was used, and the same procedure as in Reference Example (1) was carried out except that an aqueous solution of cesium carbonate was added so that cesium carbonate was 5 μmol per 1 mol of the dihydroxy compound. The resulting polycarbonate resin had a viscosity average molecular weight of 10,200 and a melt viscosity of 1,641 Poise.

(Reference Example 3) Synthesis of PC (a3) A polycarbonate resin was obtained in the same manner as in Reference Example 1 except that a predetermined predetermined stirring power value at the end of the stirrer of the second reactor was changed. The obtained polycarbonate resin had a viscosity average molecular weight of 33,000 and a melt viscosity of 18,195 poise.

(Reference Example 4) Synthesis of PC (a4) 100 parts by weight of Bis-OCZ, 272.1 parts by weight of 25% by weight sodium hydroxide (NaOH) aqueous solution and 411.3 parts by weight of water as the raw dihydroxy compound were hydrosulfite In the presence of 0.339 parts by weight, it was dissolved at 60 ° C. and then cooled to room temperature to obtain a Bis-OCZ aqueous solution. This Bis-OCZ aqueous solution (8.87 kg / hour) and methylene chloride (4.37 kg / hour) were introduced into a 1.8 L glass first reactor having a reflux condenser, a stirrer, and a refrigerant jacket, and supplied separately here. Room temperature phosgene 0.775 kg / hr. The reaction temperature at this time reached 38 ° C. Next, this reaction liquid and reaction gas were introduced into a second reactor (1.8 L) having the same shape as that of the next first reactor through an overflow pipe attached to the reactor, and reacted. Separately, 0.037 kg / hour of pt-butylphenol (8 wt% methylene chloride solution) was introduced into the second reactor as a molecular weight regulator. Subsequently, the reaction liquid and the reaction gas were introduced into an oligomerization tank (4.5 L) having the same shape as that of the first reactor from an overflow pipe attached to the second reactor. As an additional catalyst, 0.016 kg / hour (0.00083 mol per 1 mol of Bis-OCZ) was introduced into the oligomerization tank as a catalyst. Next, the oligomerized emulsion thus obtained was further introduced into a separation tank (settler) having an internal volume of 5.4 L, and the aqueous phase and the oil tank were separated to obtain an oligomeric methylene chloride solution.
Of the above oligomeric methylene chloride solution, 2.44 kg was charged into a reaction vessel equipped with a paddle blade with an internal volume of 6.8 L, and 2.60 kg of methylene chloride for dilution was added thereto. 245 kg, 0.953 kg of water, and 8.39 g of a 2 wt% triethylamine aqueous solution were added, and the mixture was stirred at 10 ° C. and subjected to a polycondensation reaction for 180 minutes.
3.12 kg of the above polycondensation reaction solution was charged into a reaction vessel equipped with a paddle blade with an internal volume of 5.4 L, added with 2.54 kg of methylene chloride and 0.575 kg of water, stirred for 15 minutes, and then stopped. The aqueous phase and the organic phase were separated. To the separated organic phase, 1.16 kg of 0.1N hydrochloric acid was added and stirred for 15 minutes to extract triethylamine and a small amount of remaining alkali component, and then stirring was stopped to separate the aqueous phase and the organic phase. Further, 1.16 kg of pure water was added to the separated organic phase, and the mixture was stirred for 15 minutes, and then the stirring was stopped to separate the aqueous phase and the organic phase. This operation was repeated three times. The obtained polycarbonate solution was pulverized by feeding into warm water at 60 to 75 ° C. and dried to obtain a powdery polycarbonate resin. The obtained polycarbonate resin had a viscosity average molecular weight of 49,900 and a melt viscosity of 127,200 poise.

Reference Example 5 Synthesis of PC (a5): Synthesis of CDOBC / BPA (50/50 wt%) copolymer (melting method)
BPA 20.62 kg (about 90 mol), 1,1 bis (4-hydroxy-3-methylphenyl) cyclododecane (hereinafter sometimes abbreviated as “CDOBC”) as a raw material dihydroxy compound (produced by Taoka Chemical Co., Ltd.) 20 .62 kg (about 54 mol) was used, and the same procedure as in Reference Example 3 was carried out except that the mixture was prepared by adding an aqueous solution of cesium carbonate so that cesium carbonate was 1 μmol per 1 mol of the dihydroxy compound. The resulting polycarbonate resin had a viscosity average molecular weight of 11,700 and a pencil hardness of 2H.

(2) Polycarbonate resin (b):
Reference Example 6 PC (b1): BPA homopolymer (melting method):
As the PC (b1), a commercially available polycarbonate resin (M7022J manufactured by Mitsubishi Engineering Plastics Co., Ltd.) by a melting method composed only of structural units derived from BPA was used. The viscosity average molecular weight of the PC (b1) was 20,600, and the melt viscosity was 9,010 Poise.

Reference Example 7 PC (b2): BPA homopolymer (melting method):
As the PC (b2), a commercially available polycarbonate resin (M7027J, manufactured by Mitsubishi Engineering Plastics Co., Ltd.) formed by a melting method composed only of structural units derived from BPA was used. The viscosity average molecular weight of the PC (b2) was 25,600, and the melt viscosity was 22,120 Poise.

(Reference Example 8) Synthesis of PC (b3) Reference Example, except that 3.4 kg of BPC (manufactured by Honshu Chemical) and 30.5 kg of BPA (manufactured by Mitsubishi Chemical) were used instead of BPC as the raw dihydroxy compound. 3 was carried out to obtain a polycarbonate resin. The viscosity average molecular weight of the obtained polycarbonate resin was 21,000.

(Reference Example 9) Synthesis of PC (b4) Instead of BPC, 3.4 kg of Bis-OCZ (Honshu Chemical) and 30.9 kg of BPA (Mitsubishi Chemical) were used as the raw dihydroxy compound. The same procedure as in Reference Example 3 was carried out to obtain a polycarbonate resin. The viscosity average molecular weight of the obtained polycarbonate resin was 19,800.

"Example 1"
As a polycarbonate resin (a) and a polycarbonate resin (b), each of PC (a1) and PC (b1) in the ratio shown in Table 1 is a Nippon Steel Works twin screw extruder (LABOTEX30HSS-32). The mixture was melt-kneaded, extruded into a strand form from the exit of the twin-screw extruder, cooled and solidified with water, and then pelletized with a rotary cutter to obtain a polycarbonate resin composition. At this time, the barrel temperature of the twin screw extruder was 280 ° C., and the temperature of the polycarbonate resin at the outlet of the twin screw extruder was 300 ° C. During melt kneading, the vent port of the twin screw extruder was connected to a vacuum pump, and the pressure at the vent port was controlled to 500 Pa.
The polycarbonate resin composition was evaluated for surface hardness, glass transition temperature (Tg), Charpy impact strength, and yellow index (YI) according to the method described in the above evaluation items. The results are shown in Table 1.
Further, the polycarbonate resin composition was evaluated for pencil hardness and yellow index (YI) as an extruded product (sheet) by the above-described method. The results are also shown in Table 1.

"Examples 3, 4, 6" and "Reference Example A"
The same procedure as in Example 1 was carried out except that the two types of polycarbonate resins shown in Table 1 were used, and the polycarbonate resin compositions of Examples 3, 4, 6 and Reference Example A were obtained.
The polycarbonate resin composition was evaluated for surface hardness, glass transition temperature (Tg), Charpy impact strength, and yellow index (YI) according to the method described in the above evaluation items. The results are shown in Table 1.
Furthermore, the polycarbonate resin composition of Example 3 was evaluated for pencil hardness and yellow index (YI) as an extruded product (sheet) by the above-described method. The results are also shown in Table 1.

"Example 5"
As the polycarbonate resin (a) and the polycarbonate resin (b), the pellets of PC (a1) and the pellets of PC (b1) were dry blended in the ratios shown in Table 1 to obtain the polycarbonate resin composition of Example 5.
The polycarbonate resin composition was evaluated for surface hardness, glass transition temperature (Tg), Charpy impact strength, and yellow index (YI) according to the method described in the above evaluation items. The results are shown in Table 1.
Further, the polycarbonate resin composition was evaluated for pencil hardness and yellow index (YI) as an extruded product (sheet) by the above-described method. The results are also shown in Table 1.

"Comparative Examples 1-4"
Except having set it as two types of polycarbonate resin shown in Table 1, it implemented similarly to Example 1, and obtained the polycarbonate resin composition of Comparative Examples 1-4.
The polycarbonate resin composition was evaluated for surface hardness, glass transition temperature (Tg), Charpy impact strength, and yellow index (YI) according to the method described in the above evaluation items. The results are shown in Table 1.
Furthermore, the polycarbonate resin composition of Comparative Example 1 was evaluated for pencil hardness and yellow index (YI) as an extruded product (sheet) by the above method. The results are also shown in Table 1.

"Comparative Examples 5-8"
PC (b1) as Comparative Example 5, PC (a1) as Comparative Example 6, PC (b3) as Comparative Example 7, PC (b4) as Comparative Example 8 alone, surface hardness, glass transition temperature (Tg), Charpy impact strength The results of evaluating the yellow index (YI) are also shown in Table 1.
Furthermore, the polycarbonate resin compositions of Comparative Examples 5 to 7 were evaluated for pencil hardness and yellow index (YI) as extruded products (sheets) by the above method. The results are also shown in Table 1.

  In Example 1 and Comparative Example 7, since the blending ratio of the dihydroxy compound is the same, it can be estimated that the content of the structural unit derived from each dihydroxy compound is the same. 1 shows that the pencil hardness defined by ISO 15184 is 2 ranks higher than the pencil hardness of Comparative Example 7. In addition, also in the yellow index (YI), Example 1 is better than Comparative Example 7. Also in Example 2 and Comparative Example 8 in which the content of structural units derived from each dihydroxy compound can be estimated to be the same as described above, the pencil hardness of Example 2 is significantly higher than that of Comparative Example 8. Are better. Moreover, when Example 1 and Comparative Example 1 and Example 2 and Comparative Example 3 are compared, if the weight ratio of the polycarbonate resin (a) and the polycarbonate resin (b) exceeds a specific range, the glass transition temperature (Tg). It can be seen that the Charpy impact strength and the yellow index (YI) are significantly deteriorated. Further, comparing Example 3 with Comparative Example 2 and Example 4 with Comparative Example 4, if the melt viscosity of the polycarbonate resin (a) and the melt viscosity of the polycarbonate resin (b) do not satisfy a specific range, the Charpy impact strength is It can be seen that the yellow index (YI) has deteriorated significantly.

  According to the present invention, it is possible to obtain a polycarbonate resin composition and a molded product having a surface hardness greatly improved, a good color tone, and a balance between impact resistance and moldability by a simple method.・ It is possible to expand the field of application to applications that require surface hardness, such as the field of electrical and electronic equipment such as personal computers, the field of automobiles such as headlamp lenses and vehicle windows, and the field of building materials such as lighting and exterior. Become.

Claims (10)

A polycarbonate resin composition comprising a polycarbonate resin (a) and a polycarbonate resin (b) having a structural unit different from the polycarbonate resin (a),
A polycarbonate resin composition characterized by satisfying the following conditions.
(I) The pencil hardness specified by ISO 15184 of the polycarbonate resin (a) is higher than the pencil hardness specified by ISO 15184 of the polycarbonate resin (b) (ii) the polycarbonate resin (a) in the polycarbonate resin composition; The weight ratio with respect to the polycarbonate resin (b) is in the range of 1:99 to 45:55 (iii) The melt viscosity of the polycarbonate resin (b) at a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ is the polycarbonate resin (a ) At a temperature of 280 ° C. and a shear rate of 122 sec ⁻¹ (iv) The polycarbonate resin (a) contains a structural unit derived from a compound represented by the following formula (1a) or (1c) And a structural unit derived from the compound represented by formula (1a) or (1c) As the weight ratio of the unit / other structural units, 100: 0 to 50: which contains between 50


(V) The polycarbonate resin (b) contains 80% by weight or more of a structural unit derived from the compound represented by the following formula (2).

(Vi) The Charpy impact strength value of the polycarbonate resin composition is 9 kJ / m ² or more.   The polycarbonate resin composition according to claim 1, wherein the polycarbonate resin (a) has a pencil hardness defined by ISO 15184 of F or more.   The polycarbonate resin composition according to claim 1 or 2, wherein the polycarbonate resin composition has a pencil hardness defined by ISO 15184 of HB or more.   The polycarbonate resin composition according to any one of claims 1 to 3, wherein YI of the polycarbonate resin composition is 4.0 or less.   The polycarbonate resin composition according to any one of claims 1 to 4, wherein a weight ratio of the polycarbonate resin (a) to the polycarbonate resin (b) is 5:95 to 40:60. A polycarbonate resin composition.   The method for producing a polycarbonate resin composition according to any one of claims 1 to 5, wherein the polycarbonate resin (a) and the polycarbonate resin (b) are melt-kneaded. Manufacturing method.   The method for producing a polycarbonate resin composition according to any one of claims 1 to 5, wherein the polycarbonate resin (a) and the polycarbonate resin (b) are dry blended. Manufacturing method.   An injection-molded article obtained by injection-molding the polycarbonate resin composition according to any one of claims 1 to 5.   An extruded product obtained by extrusion molding the polycarbonate resin composition according to any one of claims 1 to 5.   The extruded product according to claim 9, wherein the extruded product is a sheet or a film.