TECHNICAL FIELD

The present invention relates to a polycarbonate-based resin composition containing a white pigment and a molded article thereof, and more specifically, to a polycarbonate-based resin composition and a molded article thereof excellent in appearance and impact resistance.

BACKGROUND ART

A polycarbonate resin is excellent in mechanical strength, electrical characteristics, transparency, and the like, and hence has been widely utilized as an engineering plastic in various fields, such as the field of electrical and electronic equipment, and the field of automobiles. And also, the polycarbonate resin is utilized in a casing for a cellular phone, a mobile personal computer, a digital camera, a video camera, an electric tool, or the like. In these applications, impact resistance is important because of a possibility of dropping during handling in these application. In addition, a design property (especially a color) is also an important factor.

A resin material can be relatively easily colored and a colorful resin material has been used in many everyday things. In particular, a resin material having, for example, a white or gray color is frequently used. Meanwhile, a polycarbonate-polyorganosiloxane copolymer (hereinafter sometimes referred to as “PC-POS”) obtained by copolymerizing a polyorganosiloxane has been known. The PC-POS has been expected to find use in the above applications because the PC-POS is excellent in properties, such as impact resistance. Titanium oxide is desirably used as a pigment in the applications because while impact resistance is important, a design property is also important.

A composition obtained by combining a PC-POS and titanium oxide, the composition having a white external appearance and a satisfactory impact strength, has been known. For example, a polycarbonate-based resin composition that is excellent in mechanical properties, such as impact resistance and rigidity, optical characteristics, and the like, and that is also excellent in reflectance characteristic (see Patent Document 1) has been known. According to Patent Document 1, a PC-POS-containing composition whose titanium oxide content has been set to 5 to 10% shows a satisfactory reflectance and a satisfactory mechanical strength. In another example, a polycarbonate-based resin composition that shows excellent flame retardancy without a phosphorus-based flame retardant nor a halogen-based flame retardant, that has high reflectivity and a high light-shielding property, and that is excellent in thermal stability has been known (see Patent Document 2). According to Patent Document 2, a PC-POS-containing composition whose titanium oxide content has been set to 5 to 50% shows a satisfactory reflectance, a satisfactory Izod impact strength, and satisfactory flame retardancy.

The compositions disclosed in those Documents show high light-reflecting characteristics, but meanwhile, their strengths are lower than a strength inherent in a PC-POS because their titanium oxide contents are large. In addition, in the above applications, the specific gravities of the compositions were larger than a proper value. Accordingly, the development of a PC-POS-containing composition reduced in titanium oxide content while having a satisfactory reflectance, a satisfactory mechanical strength, and the like has been desired.

A composition containing a relatively small amount (e.g., 1 to 2.5 wt %) of titanium oxide and a PC-POS has also been known (see Patent Document 3).

In the PC-POS-containing composition disclosed in Patent Document 3, titanium oxide has been used in a small amount as means for improving its flame retardancy. In this Document, however, there is no disclosure concerning its color appearance.

In Patent Document 4, there is a disclosure of a polycarbonate-based resin composition excellent in appearance and impact resistance of a molded product as a result of the use of a PC-POS whose polyorganosiloxane (hereinafter sometimes referred to as “POS”) moiety has a short chain length and a PC-POS whose POS moiety has a long chain length. In Patent Document 4, a polycarbonate-based resin composition that is free of the occurrence of a black streak or the like and is hence excellent in surface appearance can be obtained, but a problem in that its impact resistance, in particular its impact resistance at low temperature is not sufficient occurs.

CITATION LIST
Patent Document

Patent Document 1: JP 05-320519 A

Patent Document 2: JP 2004-91567 A

Patent Document 3: JP 2007-509208 A

Patent Document 4: WO 2013/051557 A1

SUMMARY OF INVENTION
Technical Problem

An object of the present invention is to provide a polycarbonate-based resin composition containing a white pigment, the composition being excellent in appearance of molded product and being improved in impact resistance at low temperature, and a molded article thereof.

Solution to Problem

The inventors of the present invention have found that the object is achieved by controlling the molecular weight distribution of the polyorganosiloxane block of a polycarbonate-polyorganosiloxane copolymer in a polycarbonate-based resin composition within a specific region.

That is, the present invention relates to the following items 1 to 21.

1. A polycarbonate-based resin composition, comprising a polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer (E-1), and 0.5 to 5 parts by mass of a white pigment with respect to 100 parts by mass of the polycarbonate-based resin, wherein:

the polycarbonate-polyorganosiloxane copolymer (E-1) has a polycarbonate block (A) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B) containing a repeating unit represented by the following general formula (II); and

in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.0, and

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%:

[Image Omitted]

wherein R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂—, —O—, or —CO—, R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a and b each independently represent an integer of 0 to 4.

2. A polycarbonate-based resin composition, comprising a polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer (E-1), and 0.5 to 5 parts by mass of a white pigment with respect to 100 parts by mass of the polycarbonate-based resin, wherein:

the polycarbonate-polyorganosiloxane copolymer (E-1) has a polycarbonate block (A) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B) containing a repeating unit represented by the following general formula (II); and

the polycarbonate-based resin composition uses, as a raw material, a polyorganosiloxane having the following features: in a differential molecular weight distribution curve obtained from measurement by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.0, and

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%:

[Image Omitted]

wherein R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂⁻, —O—, or —CO—, R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a and b each independently represent an integer of 0 to 4.

3. A polycarbonate-based resin composition, comprising a polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer, and 0.5 to 5 parts by mass of a white pigment with respect to 100 parts by mass of the polycarbonate-based resin, wherein:

the polycarbonate-polyorganosiloxane copolymer comprises a polycarbonate-polyorganosiloxane copolymer (E′-1) having a polycarbonate block (A′) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B′) containing a repeating unit represented by the following general formula (II);

in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B′) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1′) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.5,

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40% or less, and

(3) a product of, a log (M) value at which the dw/d log (M) value becomes maximum and a percentage (%) of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve, is 20 to 130; and

the composition has an Izod impact strength at −40° C. of 30 kJ/m²or more:

[Image Omitted]

wherein R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂⁻, —O—, or —CO—, R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a and b each independently represent an integer of 0 to 4.

4. The polycarbonate-based resin composition according to any one of Items 1 to 3, wherein the polyorganosiloxane block (B) or the polyorganosiloxane block (B′) has an average chain length of 30 to 85.

5. The polycarbonate-based resin composition according to any one of Items 1 to 4, wherein a content of the polyorganosiloxane block (B) in the polycarbonate-polyorganosiloxane copolymer (E-1) or a content of the polyorganosiloxane block (B′) in the polycarbonate-polyorganosiloxane copolymer (E′-1) is 0.5 to 20.0 mass %.

6. The polycarbonate-based resin composition according to any one of Items 1 to 5, wherein the polycarbonate-polyorganosiloxane copolymer (E-1) or the polycarbonate-polyorganosiloxane copolymer (E′-1) has a viscosity-average molecular weight of 12,000 to 40,000.

7. The polycarbonate-based resin composition according to any one of Items 1 to 6, wherein in the general formula (I), a and b each represent 0, and X represents a single bond or an alkylidene group having 2 to 8 carbon atoms.

8. The polycarbonate-based resin composition according to any one of Items 1 to 7, wherein in the general formula (I), a and b each represent 0, and X represents an alkylidene group having 3 carbon atoms.

9. The polycarbonate-based resin composition according to any one of Items 1 to 8, wherein in the general formula (II), R³and R⁴each represent a methyl group.

10. The polycarbonate-based resin composition according to any one of Items 1 to 9, wherein a content of the polycarbonate-polyorganosiloxane copolymer (E-1) in the polycarbonate-based resin or a content of the polycarbonate-polyorganosiloxane copolymer (E′-1) in the polycarbonate-based resin is 10 mass % or more.

11. The polycarbonate-based resin composition according to any one of Items 1 to 10, wherein a content of the polyorganosiloxane block (B) in the polycarbonate-based resin or a content of the polyorganosiloxane block (B′) in the polycarbonate-based resin is 0.5 to 20.0 mass %.

12. The polycarbonate-based resin composition according to any one of Items 1 to 11, wherein the white pigment comprises at least one selected from titanium oxide, zinc oxide, talc, barium sulfate, calcium carbonate and zinc sulfide.

13. The polycarbonate-based resin composition according to Item 12, wherein the white pigment comprises titanium oxide.

14. The polycarbonate-based resin composition according to Item 13, wherein the titanium oxide comprises titanium oxide coated with at least one selected from a polyol compound, an amine compound, alumina, silica and a polyorganosiloxane.

15. The polycarbonate-based resin composition according to Item 14, wherein the titanium oxide comprises titanium oxide coated with a polyol compound.

16. The polycarbonate-based resin composition according to Item 15, wherein the polyol compound comprises at least one selected from trimethylolpropane, trimethylolethane, ditrimethylolpropane, trimethylolpropane ethoxylate and pentaerythritol.

17. The polycarbonate-based resin composition according to any one of Items 1 to 16, further comprising 0.001 to 0.5 parts by mass of an antioxidant with respect to 100 parts by mass of the polycarbonate-based resin.

18. The polycarbonate-based resin composition according to any one of Items 1 to 17, further comprising 0.01 to 1.0 part by mass of a UV absorber with respect to 100 parts by mass of the polycarbonate-based resin.

19. A molded article, comprising the polycarbonate-based resin composition of any one of Items 1 to 18.

20. The molded article according to Item 19, wherein the molded article comprises a part for electrical and electronic equipment.

21. The molded article according to Item 20, wherein the molded article comprises a casing for electrical and electronic equipment.

Advantageous Effects of Invention

According to the present invention, the polycarbonate-based resin composition containing a white pigment, the composition being excellent in appearance of molded article and being improved in impact resistance at low temperature, and the molded article thereof can be obtained by controlling the molecular weight distribution of the polyorganosiloxane block of the polycarbonate-polyorganosiloxane copolymer in the polycarbonate-based resin composition within a specific region.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a graph for showing an example of the differential molecular weight distribution curve of a polyorganosiloxane to be used as a production raw material for a polycarbonate-polyorganosiloxane copolymer to be used in a polycarbonate-based resin composition of the present invention.

FIG. 2 is a photograph for showing a molded article including a sprue and a runner, and a test piece for performing each test.

DESCRIPTION OF EMBODIMENTS

A polycarbonate-based resin composition according to a first embodiment of the present invention comprises a polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer (E-1), and 0.5 to 5 parts by mass of a white pigment with respect to 100 parts by mass of the polycarbonate-based resin, wherein:

the polycarbonate-polyorganosiloxane copolymer (E-1) has a polycarbonate block (A) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B) containing a repeating unit represented by the following general formula (II); and

in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.0, and

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%:

[Image Omitted]

wherein R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂⁻, —O—, or —CO—, R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a and b each independently represent an integer of 0 to 4.

A polycarbonate-based resin composition according to a second embodiment of the present invention comprises a polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer, and 0.5 to 5 parts by mass of a white pigment with respect to 100 parts by mass of the polycarbonate-based resin, wherein:

the polycarbonate-polyorganosiloxane copolymer comprises a polycarbonate-polyorganosiloxane copolymer (E′-1) having a polycarbonate block (A′) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B′) containing a repeating unit represented by the following general formula (II);

in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B′) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1′) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.5,

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40% or less, and

(3) a product of, a log (M) value at which the dw/d log (M) value becomes maximum and a percentage (%) of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve, is 20 to 130; and

the composition has an Izod impact strength at −40° C. of 30 kJ/m²or more:

[Image Omitted]

wherein R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂⁻, —O—, or —CO—, R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a and b each independently represent an integer of 0 to 4.

That is, according to the first embodiment of the present invention, the polycarbonate-based resin composition comprises, as the polycarbonate-based resin, the polycarbonate-polyorganosiloxane copolymer (E-1) having the polyorganosiloxane block (B) having the predetermined molecular weight distribution. The polycarbonate-based resin composition according to the first embodiment may comprise, as the polycarbonate-based resin, a polycarbonate-polyorganosiloxane copolymer except the (E-1).

According to the second embodiment of the present invention, the polycarbonate-based resin composition comprises the polycarbonate-polyorganosiloxane copolymer as the polycarbonate-based resin, wherein the polycarbonate-polyorganosiloxane copolymer is the polycarbonate-polyorganosiloxane copolymer (E′-1) having the polyorganosiloxane block (B′) having the predetermined molecular weight distribution. The polycarbonate-polyorganosiloxane copolymer (E′-1) may be formed of one of polycarbonate-polyorganosiloxane copolymer, or may be formed of a mixture of two or more of polycarbonate-polyorganosiloxane copolymers. Therefore, for example, when the (E′-1) is formed of a mixture of two or more of polycarbonate-polyorganosiloxane copolymers, the “polyorganosiloxane block (B′) containing a repeating unit represented by the general formula (II)” in the (E′-1) refers to a polyorganosiloxane block in the mixture.

In the following description, the term “polycarbonate-based resin composition of the present invention” refers to both the polycarbonate-based resin compositions of the first embodiment and the second embodiment unless otherwise stated.

In addition, in the following description, the polycarbonate block (A), the polyorganosiloxane block (B), and the PC-POS copolymer (E-1) in the polycarbonate-based resin composition of the first embodiment, and their preferred modes, and the polycarbonate block (A′), the polyorganosiloxane block (B′), and the PC-POS copolymer (E′-1) in the polycarbonate-based resin composition of the second embodiment, and their preferred modes are identical to each other unless otherwise stated.

[Polycarbonate-Based Resin]

The polycarbonate-based resin containing the polycarbonate-polyorganosiloxane copolymer (E-1) is used in the polycarbonate-based resin composition according to the first embodiment of the present invention. The polycarbonate-polyorganosiloxane copolymer (E-1) is described below.

The polycarbonate-polyorganosiloxane copolymer (E-1) is required to have the following features:

the polycarbonate-polyorganosiloxane copolymer (E-1) has a polycarbonate block (A) formed of a repeating unit represented by the following general formula (I) and a polyorganosiloxane block (B) containing a repeating unit represented by the following general formula (II); and

in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.0, and

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%:

[Image Omitted]

In the general formula (I), R¹and R²each independently represent a halogen atom, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, X represents a single bond, an alkylene group having 1 to 8 carbon atoms, an alkylidene group having 2 to 8 carbon atoms, a cycloalkylene group having 5 to 15 carbon atoms, a cycloalkylidene group having 5 to 15 carbon atoms, a fluorenediyl group, an arylalkylene group having 7 to 15 carbon atoms, an arylalkylidene group having 7 to 15 carbon atoms, —S—, —SO—, —SO₂—, —O—, or —CO—, and a and b each independently represent an integer of 0 to 4.

In the general formula (II), R³and R⁴each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms.

Examples of the halogen atom that R¹and R²in the general formula (I) each independently represent include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.

Examples of the alkyl group that R¹and R²each independently represent include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, various butyl groups (“various” means that a linear group and any branched group are included, and the same applies hereinafter), various pentyl groups, and various hexyl groups. An example of the alkoxy group that R¹and R²each independently represent is an alkoxy group whose alkyl group moiety is the alkyl group described above.

The alkylene group represented by X is, for example, a methylene group, an ethylene group, a trimethylene group, a tetramethylene group, or a hexamethylene group, and is preferably an alkylene group having 1 to 5 carbon atoms. Examples of the alkylidene group represented by X include an ethylidene group and an isopropylidene group. The cycloalkylene group represented by X is, for example, a cyclopentanediyl group, a cyclohexanediyl group, or a cyclooctanediyl group, and is preferably a cycloalkylene group having 5 to 10 carbon atoms. The cycloalkylidene group represented by X is, for example, a cyclohexylidene group, a 3,5,5-trimethylcyclohexylidene group, or a 2-adamantylidene group, and is preferably a cycloalkylidene group having 5 to 10 carbon atoms, more preferably a cycloalkylidene group having 5 to 8 carbon atoms. As an aryl moiety of the arylalkylene group represented by X, there are given, for example, aryl groups each having 6 to 14 ring-forming carbons, such as a phenyl group, a naphthyl group, a biphenyl group, and an anthryl group. As an aryl moiety of the arylalkylidene group represented by X, there are given, for example, aryl groups each having 6 to 14 ring-forming carbons, such as a phenyl group, a naphthyl group, a biphenyl group, and an anthryl group.

a and b each independently represent an integer of 0 to 4, preferably 0 to 2, more preferably 0 or 1.

Among them, the following is suitable: a repeating unit in which a and b each represent 0, and X represents a single bond or an alkylidene group having 2 to 8 carbon atoms, or a repeating unit in which a and b each represent 0, and X represents an alkylidene group having 3 carbon atoms, particularly an isopropylidene group.

Examples of the halogen atom represented by R³or R⁴in the general formula (II) include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Examples of the alkyl group represented by R³or R⁴include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, various butyl groups, various pentyl groups, and various hexyl groups. An example of the alkoxy group represented by R³or R⁴is an alkoxy group whose alkyl group moiety is the alkyl group described above. Examples of the aryl group represented by R³or R⁴include a phenyl group and a naphthyl group.

R³and R⁴each preferably represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and each more preferably represent a methyl group.

The content of the polyorganosiloxane block (B) containing a repeating unit represented by the general formula (II) in the polycarbonate-polyorganosiloxane copolymer (E-1) to be used in the present invention is preferably 0.5 to 20.0 mass %, more preferably 1.5 to 15.0 mass %. When the content of the polyorganosiloxane block (B) is 0.5 mass % or more, sufficient low-temperature impact resistance is obtained, and when the content is 20.0 mass % or less, sufficient heat resistance is obtained.

The polyorganosiloxane block (B) containing a repeating unit represented by the general formula (II) in the PC-POS copolymer (E-1) to be used in the present invention is preferably represented by any one of the following general formulae (ii-I) to (ii-III):

[Image Omitted]

wherein R³to R⁶each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a plurality of R³, R⁴, R⁵, or R⁶may be identical to or different from each other, Y represents —R⁷O—, —R⁷COO—, —R⁷NH—, —R⁷NR⁸—, —COO—, —S—, —R⁷COO—R⁹—O—, or —R⁷O—R¹⁶—O—, and a plurality of Y may be identical to or different from each other, the R⁷represents a single bond, a linear, branched or cyclic alkylene group, an aryl-substituted alkylene group, a substituted or unsubstituted arylene group, or a diarylene group, R⁸represents an alkyl group, an alkenyl group, an aryl group or an aralkyl group, R⁹represents a diarylene group, R¹⁰represents a linear, branched or cyclic alkylene group, or a diarylene group, β represents a divalent group derived from a diisocyanate compound, or a divalent group derived from a dicarboxylic acid or a halide of a dicarboxylic acid, p and q each represent an integer of 1 or more, and the sum of p and q is n−2, and n represents an average chain length.

Examples of the halogen atom that R³to R⁶each independently represent include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. Examples of the alkyl group that R³to R⁶each independently represent include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, various butyl groups, various pentyl groups and various hexyl groups. An example of the alkoxy group that R³to R⁶each independently represent is an alkoxy group whose alkyl group moiety is the alkyl group described above. Examples of the aryl group that R³to R⁶each independently represent include a phenyl group and a naphthyl group.

R³to R⁶each preferably represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms.

R³to R⁶in the general formula (ii-I), the general formula (ii-II), and/or the general formula (ii-III) each preferably represent a methyl group.

The linear or branched alkylene group represented by R⁷in —R⁷O—, —R⁷COO—, —R⁷NH—, —R⁷NR⁸—, —R⁷COO—R⁹—O— or —R⁷O—R¹⁰—O— represented by Y is, for example, an alkylene group having 1 to 8, preferably 1 to 5 carbon atoms, and the cyclic alkylene group represented by R⁷is, for example, a cycloalkylene group having 5 to 15, preferably 5 to 10 carbon atoms.

The average chain length n of the polyorganosiloxane block (B) in the polycarbonate-polyorganosiloxane copolymer (E-1) to be used in the present invention is preferably 30 to 85, more preferably 40 to 75, and still more preferably 58 to 72. The average chain length is calculated by nuclear magnetic resonance (NMR) measurement. When the average chain length n is 30 or more, a resin composition and a molded article each having sufficient impact resistance at low temperature can be obtained. In addition, when the average chain length n is 85 or less, a resin composition and a molded article each of which is excellent in appearance of molded product can be obtained.

The polyorganosiloxane block (B) containing a repeating unit represented by the general formula (II) for forming the polycarbonate-polyorganosiloxane copolymer (E-1) to be used in the present invention has a feature in that in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.0, and

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%.

In order that the polyorganosiloxane block (B) for forming the polycarbonate-polyorganosiloxane copolymer (E-1) to be used in the present invention may have the above feature, a polyorganosiloxane represented by the following general formula (2), the following general formula (3), and/or the following general formula (4) can be used as a raw material:

[Image Omitted]

wherein R³to R⁶each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms, and a plurality of R³, R⁴, R⁵, or R⁶may be identical to or different from each other, Y represents —R⁷O—, —R⁷COO—, —R⁷NH—, —R⁷NR⁸—, —COO—, —S—, —R⁷COO—R⁹—O—, or —R⁷O—R¹⁰—O—, and a plurality of Y may be identical to or different from each other, the R⁷represents a single bond, a linear, branched or cyclic alkylene group, an aryl-substituted alkylene group, a substituted or unsubstituted arylene group or a diarylene group, R⁸represents an alkyl group, an alkenyl group, an aryl group or an aralkyl group, R⁹represents a diarylene group, R¹⁰represents a linear, branched or cyclic alkylene group, or a diarylene group, Z represents a hydrogen atom or a halogen atom and a plurality of Z may be identical to or different from each other, β represents a divalent group derived from a diisocyanate compound, or a divalent group derived from a dicarboxylic acid or a halide of a dicarboxylic acid, p and q each represent an integer of 1 or more, and the sum of p and q is n−2, and n represents an average chain length.

Examples of the halogen atom that R³to R⁶each independently represent include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Examples of the alkyl group that R³to R⁶each independently represent include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, various butyl groups, various pentyl groups, and various hexyl groups. An example of the alkoxy group that R³to R⁶each independently represent is an alkoxy group whose alkyl group moiety is the alkyl group described above. Examples of the aryl group that R³to R⁶each independently represent include a phenyl group and a naphthyl group.

R³to R⁶each preferably represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms.

The polyorganosiloxane represented by the general formula (2), the general formula (3) and/or the general formula (4) is preferably a polyorganosiloxane in which R³to R⁶each represent a methyl group.

The linear or branched alkylene group represented by R⁷in —R⁷O—, —R⁷COO—, —R⁷NH—, —R⁷NR⁸—, —R⁷COO—R⁹—O— or represented by Y is, for example, an alkylene group having 1 to 8, preferably 1 to 5 carbon atoms, and the cyclic alkylene group represented by R⁷is, for example, a cycloalkylene group having 5 to 15, preferably 5 to 10 carbon atoms.

The aryl-substituted alkylene group represented by R⁷may have a substituent, such as an alkoxy group or an alkyl group, on its aromatic ring, and a specific structure thereof may be, for example, a structure represented by the following general formula (5) or (6), provided that when the block has the aryl-substituted alkylene group, the alkylene group is bonded to Si:

[Image Omitted]

wherein c represents a positive integer and typically represents an integer of 1 to 6.

The diarylene group represented by any one of R⁷, R⁹, and R¹⁰is a group in which two arylene groups are linked to each other directly or through a divalent organic group, and is specifically a group having a structure represented by —Ar¹—W—Ar²—. Here, Ar¹and Ar²each represent an arylene group, and W represents a single bond or a divalent organic group. Examples of the divalent organic group represented by W include an isopropylidene group, a methylene group, a dimethylene group and a trimethylene group.

Examples of the arylene group represented by any one of R⁷, Ar¹and Ar²include arylene groups each having 6 to 14 ring-forming carbon atoms, such as a phenylene group, a naphthylene group, a biphenylene group, and an anthrylene group. Those arylene groups may each have an arbitrary substituent, such as an alkoxy group or an alkyl group.

The alkyl group represented by R⁸is a linear or branched group having 1 to 8, preferably 1 to 5 carbon atoms. The alkenyl group represented by R⁸is, for example, a linear or branched group having 2 to 8, preferably 2 to 5 carbon atoms. The aryl group represented by R⁸is, for example, a phenyl group or a naphthyl group. The aralkyl group represented by R⁸is, for example, a phenylmethyl group or a phenylethyl group.

The linear, branched, or cyclic alkylene group represented by R¹⁰is the same as that represented by R⁷.

Y preferably represents —R⁷O—. R⁷preferably represents an aryl-substituted alkylene group, in particular a residue of a phenol-based compound having an alkyl group, and more preferably represents an organic residue derived from allylphenol or an organic residue derived from eugenol.

With regard top and q in the general formula (3), it is preferred that p=q, i.e., p=(n-2)/2 and q=(n-2)/2.

As described above, the average chain length n is preferably 30 to 85, more preferably 40 to 75, and still more preferably 58 to 72.

β represents a divalent group derived from a diisocyanate compound, or a divalent group derived from a dicarboxylic acid or a halide of a dicarboxylic acid, and examples thereof include divalent groups represented by the following general formulae (7-1) to (7-5).

[Image Omitted]

Examples of the polyorganosiloxane represented by the general formula (2) include compounds represented by the following general formulae (2-1) to (2-11):

[Image Omitted]

In the general formulae (2-1) to (2-11), R³to R⁶, n, and R⁸are as defined above, and preferred examples thereof are also the same as those described above, and c represents a positive integer and typically represents an integer of from 1 to 6.

Among them, a phenol-modified polyorganosiloxane represented by the general formula (2-1) is preferred from the viewpoint of its ease of polymerization. In addition, an α,ω-bis[3-(o-hydroxyphenyl)propyl]polydimethylsiloxane, which is one of compound represented by the general formula (2-2), or an α,ω-bis[3-(4-hydroxy-3-methoxyphenyl)propyl]polydimethylsiloxane, which is one of compound represented by the general formula (2-3), is preferred from the viewpoint of its ease of availability.

In addition to the polyorganosiloxane shown above, polyorganosiloxane compounds disclosed in the following Documents may also be suitably used: JP 2013-523938 A, JP 04-225059 A, JP 2006-518803 A, WO 2013/115604 A1, and the like.

The average chain length n of the polyorganosiloxane represented by the general formula is preferably 30 to 85, more preferably 40 to 75, still more preferably 58 to 72. The average chain length is calculated by nuclear magnetic resonance (NMR) measurement. When the average chain length n is 30 or more, the impact resistance at low temperature is sufficiently obtained. When the average chain length n is 85 or less, a copolymer excellent in appearance of molded product can be obtained.

A gel permeation chromatographic (GPC) apparatus for obtaining the measured values of the molecular weight and molecular weight distribution of the polyorganosiloxane is not particularly limited, and a GPC apparatus that is generally on the market such as a high-temperature GPC measuring machine with internal refractive index (RI) detector “HLC-8200” manufactured by Tosoh Corporation, can be utilized. In particular, a product obtained by coupling “TSK-GEL G4000HXL” and “TSK-GEL G2000HXL” manufactured by Tosoh Corporation is used as a GPC column. A column temperature is set to 40° C., tetrahydrofuran (THF) is used as an eluent, and measurement is performed at a flow rate of 1.0 ml/min. A standard polystyrene manufactured by Tosoh Corporation is used to obtain a calibration curve. The logarithmic value of a molecular weight thus obtained is referred to as “logarithmic molecular weight (log (M)).”

In the time curve of an intensity distribution detected with the refractive index (RI) detector of the GPC apparatus (generally referred to as “elution curve”), an elution time is converted into a molecular weight by using the calibration curve obtained from the substance having a known molecular weight. Here, the intensity detected with the RI is in proportion to a component concentration, and hence a concentration fraction at each elution time is determined by determining an intensity area when the total area of the elution curve is set to 100%. An integral molecular weight distribution curve can be obtained by sequentially integrating the concentration fraction, and plotting the logarithmic value of the molecular weight (log (M)) along an axis of abscissa and the integrated value of the concentration fraction (w) along an axis of ordinate.

Subsequently, a differential molecular weight distribution curve can be obtained by determining the differential value of the curve at each logarithmic value of the molecular weight (i.e., the gradient of the integral molecular weight distribution curve), and plotting the logarithmic value of the molecular weight (log (M)) along an axis of abscissa and the differential value (dw/d log (M)) along an axis of ordinate. Therefore, a differential molecular weight distribution means a value obtained by differentiating the concentration fraction (w) with respect to the logarithmic value of the molecular weight (log (M)), i.e., “dw/d log (M).” The differential molecular weight distribution dw/d log (M) at a specific log (M) can be read from the differential molecular weight distribution curve. It should be noted that in the case of a polyorganosiloxane blend obtained by blending a plurality of polyorganosiloxanes as well, a differential molecular weight distribution curve can be obtained by the same approach after the measurement of the polyorganosiloxane blend by a GPC method.

In the present invention, (1) the dw/d log (M) value becomes maximum in the range of 3.4≤log (M)≤4.0, preferably in the range of 3.5≤log (M)≤3.8. The maximum value of the differential molecular weight distribution dw/d log (M) refers to a peak top in the differential molecular weight distribution curve. When the value for the log (M) of the peak top in the differential molecular weight distribution curve is 3.4 or more, sufficient low-temperature impact resistance is obtained, and when the value is 4.0 or less, a satisfactory appearance is obtained.

In the present invention, (2) the ratio of a value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40% or less, preferably 6.5 to 30%. When the ratio is 6% or more, sufficient low-temperature impact resistance is obtained. When the ratio is 40% or less, a satisfactory appearance is obtained. Here, the ratio of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) refers to the ratio at which a component having a log (M) of 4.00 or more and 4.50 or less is present with respect to the entirety of the POS in the molecular weight distribution of the POS.

A method of producing the polyorganosiloxane is not particularly limited. According to, for example, a method described in JP 11-217390 A, a crude polyorganosiloxane can be obtained by: causing cyclotrisiloxane and disiloxane to react with each other in the presence of an acid catalyst to synthesize α,ω-dihydrogen organopentasiloxane; and then subjecting a phenolic compound (such as 2-allylphenol, 4-allylphenol, eugenol, or 2-propenylphenol) or the like to an addition reaction with the α,ω-dihydrogen organopentasiloxane in the presence of a catalyst for a hydrosilylation reaction. In addition, according to a method described in JP 2662310 B2, the crude polyorganosiloxane can be obtained by: causing octamethylcyclotetrasiloxane and tetramethyldisiloxane to react with each other in the presence of sulfuric acid (acid catalyst); and subjecting a phenolic compound or the like to an addition reaction with the resultant α,ω-dihydrogen organopolysiloxane in the presence of the catalyst for a hydrosilylation reaction in the same manner as described above. The chain length n of the α,ω-dihydrogen organopolysiloxane can be appropriately adjusted depending on a polymerization condition therefor before its use, or a commercially available α,ω-dihydrogen organopolysiloxane may be used.

Examples of the catalyst for a hydrosilylation reaction include transition metal-based catalysts. Among them, a platinum-based catalyst is preferably used in terms of a reaction rate and selectivity. Specific examples of the platinum-based catalyst include chloroplatinic acid, a solution of chloroplatinic acid in an alcohol, an olefin complex of platinum, a complex of platinum and a vinyl group-containing siloxane, platinum-supported silica, and platinum-supported activated carbon.

An adsorbent is preferably caused to adsorb and remove a transition metal derived from a transition metal-based catalyst used as the catalyst for a hydrosilylation reaction in the crude polyorganosiloxane by bringing the crude polyorganosiloxane into contact with the adsorbent.

An adsorbent having an average pore diameter of, for example, 1,000 Å or less can be used as the adsorbent. When the average pore diameter is 1,000 Å or less, the transition metal in the crude polyorganosiloxane can be efficiently removed. From such viewpoint, the average pore diameter of the adsorbent is preferably 500 Å or less, more preferably 200 Å or less, still more preferably 150 Å or less, yet still more preferably 100 Å or less. In addition, from the same viewpoint, the adsorbent is preferably a porous adsorbent.

The adsorbent is not particularly limited as long as the adsorbent has the above-mentioned average pore diameter. For example, there may be used activated clay, acidic clay, activated carbon, synthetic zeolite, natural zeolite, activated alumina, silica, a silica-magnesia-based adsorbent, diatomaceous earth, and cellulose. Among them, preferred is at least one selected from the group consisting of activated clay, acidic clay, activated carbon, synthetic zeolite, natural zeolite, activated alumina, silica, and a silica-magnesia-based adsorbent.

After the adsorbent has been caused to adsorb the transition metal in the crude polyorganosiloxane, the adsorbent can be separated from the polyorganosiloxane by arbitrary separating means. Examples of the means for separating the adsorbent from the polyorganosiloxane include a filter and centrifugation. When the filter is used, a filter such as a membrane filter, a sintered metal filter, or a glass fiber filter can be used. Among them, the membrane filter is particularly preferably used.

The average particle diameter of the adsorbent is typically 1 μm to 4 mm, preferably 1 μm to 100 μm from the viewpoint of separating the adsorbent from the polyorganosiloxane after the adsorption of the transition metal.

When the adsorbent is used, its usage amount is not particularly limited. A porous adsorbent can be used in an amount in the range of preferably 1 to 30 parts by mass, more preferably 2 to 20 parts by mass with respect to 100 parts by mass of the crude polyorganosiloxane.

When the crude polyorganosiloxane to be treated has so high a molecular weight that the crude polyorganosiloxane is not in a liquid state, the polyorganosiloxane may be heated to such a temperature as to be in a liquid state upon performance of the adsorption with the adsorbent and the separation of the adsorbent. Alternatively, the adsorption and the separation may be performed under a state in which the polyorganosiloxane is dissolved in a solvent, such as methylene chloride or hexane.

A polyorganosiloxane having a desired molecular weight distribution is obtained by regulating its molecular weight distribution through, for example, the blending of a plurality of polyorganosiloxanes. With regard to the blending, a crude polyorganosiloxane having a desired molecular weight distribution can be obtained by blending a plurality of α,ω-dihydrogen organopolysiloxanes and then subjecting a phenol compound or the like to an addition reaction with the resultant in the presence of a catalyst for a hydrosilylation reaction. In addition, purification, such as the removal of the catalyst for a hydrosilylation reaction, may be performed after a plurality of crude polyorganosiloxanes have been blended. A plurality of polyorganosiloxanes after the purification may be blended. In addition, a molecular weight distribution can be appropriately adjusted depending on a polymerization condition at the time of the production of a polyorganosiloxane. In addition, a desired molecular weight distribution can be obtained by fractionating only part of existing polyorganosiloxanes through means such as various kinds of separation.

A known production method, such as an interfacial polymerization method (phosgene method), a pyridine method, or an ester exchange method, can be employed as a method of producing the PC-POS copolymer (E-1) to be used in the present invention. Particularly in the case of the interfacial polymerization method, the step of separating an organic phase containing the PC-POS copolymer (E-1) and an aqueous phase containing an unreacted substance, a catalyst residue, or the like becomes easy, and hence the separation of the organic phase containing the PC-POS copolymer (E-1) and the aqueous phase in each washing step based on alkali washing, acid washing, or pure water washing becomes easy. Accordingly, the PC-POS copolymer (E-1) is efficiently obtained.

The method of producing the PC-POS copolymer (E-1) is not particularly limited and the copolymer can be produced with reference to a known method of producing a PC-POS copolymer, such as a method described in JP 2010-241943 A.

Specifically, the PC-POS copolymer (E-1) can be produced by: dissolving a polycarbonate oligomer produced in advance and the polyorganosiloxane in a water-insoluble organic solvent (such as methylene chloride); adding an alkaline aqueous solution (such as aqueous sodium hydroxide) of a dihydric phenol-based compound (such as bisphenol A) to the solution; and subjecting the mixture to an interfacial polycondensation reaction through the use of a tertiary amine (such as triethylamine) or a quaternary ammonium salt (such as trimethylbenzylammonium chloride) as a polymerization catalyst in the presence of a terminal stopper (a monohydric phenol such as p-t-butylphenol). In addition, the PC-POS copolymer (E-1) can be produced by copolymerizing a polyorganosiloxane, a dihydric phenol, and phosgene, a carbonate, or a chloroformate.

In one embodiment of the present invention, as described above, a polyorganosiloxane having the following features is used as a raw material for the copolymer: when an axis of ordinate and an axis of abscissa in a differential molecular weight distribution curve obtained from the results of measurement by the GPC method using the polystyrene calibration curve indicate dw/d log (M) and log (M), where w represents a concentration fraction and M represents a molecular weight, respectively, (1) a dw/d log (M) value becomes maximum in the range of 3.4≤log (M)≤4.0, and (2) the ratio of a value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%. Specifically, a polyorganosiloxane represented by the formula (2), the formula (3), or the formula (4) is used.

The polycarbonate oligomer can be produced through a reaction of a dihydric phenol and a carbonate precursor, such as phosgene or triphosgene, in an organic solvent, such as methylene chloride, chlorobenzene, or chloroform. When the polycarbonate oligomer is produced by using an ester exchange method, the oligomer can also be produced through a reaction of a dihydric phenol and a carbonate precursor, such as diphenyl carbonate.

A dihydric phenol represented by the following general formula (i) is preferably used as the dihydric phenol:

[Image Omitted]

wherein R¹, R², a, b, and X are as described above.

Examples of the dihydric phenol represented by the general formula (i) include a bis(hydroxyaryl)alkane, a bis(hydroxyaryl)cycloalkane, a dihydroxyaryl ether, a dihydroxydiaryl sulfide, a dihydroxydiaryl sulfoxide, a dihydroxydiaryl sulfone, a dihydroxydiphenyl, a dihydroxydiarylfluorene, and a dihydroxydiaryladamantane. Those dihydric phenols may be used alone or as a mixture thereof.

Examples of the bis(hydroxyaryl)alkane include bis(4-hydroxyphenyl)methane, 1,1-bis(4-hydroxyphenyl)ethane, 2,2-bis(4-hydroxyphenyl)propane [bisphenol A], 2,2-bis(4-hydroxyphenyl)butane, 2,2-bis(4-hydroxyphenyl)octane, bis(4-hydroxyphenyl)phenylmethane, bis(4-hydroxyphenyl)diphenylmethane, 2,2-bis(4-hydroxy-3-methylphenyl)propane, bis(4-hydroxyphenyl)naphthylmethane, 1,1-bis(4-hydroxy-3-t-butylphenyl)propane, 2,2-bis(4-hydroxy-3-bromophenyl)propane, 2,2-bis(4-hydroxy-3,5-dimethylphenyl)propane, 2,2-bis(4-hydroxy-3-chlorophenyl)propane, 2,2-bis(4-hydroxy-3,5-dichlorophenyl)propane, and 2,2-bis(4-hydroxy-3,5-dibromophenyl) propane.

Examples of the bis(hydroxyaryl)cycloalkane include 1,1-bis(4-hydroxyphenyl)cyclopentane, 1,1-bis(4-hydroxyphenyl)cyclohexane, 1,1-bis(4-hydroxyphenyl)-3,5,5-trimethylcyclohexane, 2,2-bis(4-hydroxyphenyl)norbornene, and 1,1-bis(4-hydroxyphenyl)cyclododecane. Examples of the dihydroxyaryl ether include 4,4′-dihydroxydiphenyl ether and 4,4′-dihydroxy-3,3′-dimethylphenyl ether.

Examples of the dihydroxydiaryl sulfide include 4,4′-dihydroxydiphenyl sulfide and 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfide. Examples of the dihydroxydiaryl sulfoxide include 4,4′-dihydroxydiphenyl sulfoxide and 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfoxide. Examples of the dihydroxydiaryl sulfone include 4,4′-dihydroxydiphenyl sulfone and 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfone.

An example of the dihydroxydiphenyl is 4,4′-dihydroxydiphenyl. Examples of the dihydroxydiarylfluorene include 9,9-bis(4-hydroxyphenyl)fluorene and 9,9-bis(4-hydroxy-3-methylphenyl)fluorene. Examples of the dihydroxydiaryladamantane include 1,3-bis(4-hydroxyphenyl)adamantane, 2,2-bis(4-hydroxyphenyl)adamantane, and 1,3-bis(4-hydroxyphenyl)-5,7-dimethyladamantane.

Examples of the dihydric phenol other than the above-mentioned dihydric phenols include 4,4′-[1,3-phenylenebis(1-methylethylidene)]bisphenol, 10,10-bis(4-hydroxyphenyl)-9-anthrone, and 1,5-bis(4-hydroxyphenylthio)-2,3-dioxapentane.

The dihydric phenols may be used alone or as a mixture thereof.

Among them, bis(hydroxyphenyl)alkanes are preferred, and bisphenol A is more preferred. When bisphenol A is used as the dihydric phenol, X represents an isopropylidene group and a relationship of a=b=0 is satisfied in the general formula (i).

In order to control the molecular weight of the PC-POS copolymer to be obtained, a terminal stopper can be used. Examples of the terminal stopper may include monohydric phenols, such as phenol, p-cresol, p-tert-butylphenol, p-tert-octylphenol, p-cumylphenol, p-nonylphenol, m-pentadecylphenol, and p-tert-amylphenol. Those monohydric phenols may be used alone or in combination thereof.

After the interfacial polycondensation reaction, the liquid is appropriately left at rest to be separated into an aqueous phase and an organic solvent phase [separating step], the organic solvent phase is washed (preferably washed with a basic aqueous solution, an acidic aqueous solution, and water in the stated order) [washing step], and the resultant organic phase is concentrated [concentrating step], and dried [drying step]. Thus, the PC-POS copolymer can be obtained.

The PC-POS copolymer (E-1) to be used in the present invention can be produced by appropriately using, for example, a molecular weight modifier so that its viscosity-average molecular weight may be a molecular weight intended for an application or product in which the copolymer is used. The copolymer is produced so as to have a viscosity-average molecular weight in the range of typically 12,000 to 40,000, preferably about 15,000 to about 30,000. When the viscosity-average molecular weight is 12,000 or more, the strength of a molded article is sufficient. When the viscosity-average molecular weight is 40,000 or less, injection molding or extrusion molding can be performed in a proper temperature region, and hence a satisfactory appearance is obtained.

In addition, the viscosity of the PC-POS copolymer (E-1) can be reduced by increasing its molding temperature. In that case, however, its molding cycle lengthens to result in poor economical efficiency. Moreover, when the temperature is excessively increased, the transparency tends to reduce owing to the heat deterioration of the PC-POS copolymer (E-1).

The viscosity-average molecular weight (Mv) is a value calculated from Schnell's equation ([η]=1.23×10⁻³×Mv^0.83) by measuring the limiting viscosity [η] of a methylene chloride solution at 20° C.

In addition to the polycarbonate-polyorganosiloxane copolymer (E-1), a homopolycarbonate formed of a repeating unit represented by the general formula (I) or copolymerized polycarbonate, and a polycarbonate-polyorganosiloxane copolymer except the (E-1), the copolymer having the polycarbonate block (A) formed of a repeating unit represented by the general formula (I) and the polyorganosiloxane block (B) containing a repeating unit represented by the general formula (II), can each be incorporated as the polycarbonate-based resin to be used in the polycarbonate-based resin composition according to the first embodiment of the present invention. The content of the polycarbonate-polyorganosiloxane copolymer (E-1) in the polycarbonate-based resin is preferably 10 mass % or more. The content is more preferably 20 mass % or more, still more preferably 40 mass % or more, still further more preferably 50 mass % or more and 100 mass % or less from the viewpoint that the effects of the present invention are obtained.

In addition, it is desired that the content of the polyorganosiloxane block (B) containing a repeating unit represented by the general formula (II) in the polycarbonate-based resin containing the polycarbonate-polyorganosiloxane copolymer (E-1) be set to preferably 0.5 to 20.0 mass %, more preferably 1.5 to 15.0 mass %. When the content of the polyorganosiloxane block (B) is 0.5 mass % or more, sufficient low-temperature impact resistance is obtained, and when the content is 20.0 mass % or less, sufficient heat resistance is obtained.

Next, the polycarbonate-based resin to be used in the polycarbonate-based resin composition according to the second embodiment of the present invention is described.

A polycarbonate-based resin containing a polycarbonate-polyorganosiloxane copolymer is used in the polycarbonate-based resin composition according to the second embodiment of the present invention. The polycarbonate-polyorganosiloxane copolymer is required to have the following features: the polycarbonate-polyorganosiloxane copolymer comprises a polycarbonate-polyorganosiloxane copolymer (E′-1) having a polycarbonate block (A′) formed of a repeating unit represented by the general formula (I) and a polyorganosiloxane block (B′) containing a repeating unit represented by the general formula (II); in a differential molecular weight distribution curve obtained from measurement of the polyorganosiloxane block (B′) by gel permeation chromatography using a polystyrene calibration curve, the curve having an axis of abscissa indicating a logarithmic value log (M) of a molecular weight M and an axis of ordinate indicating dw/d log (M) obtained by differentiating a concentration fraction w with respect to the logarithmic value log (M) of the molecular weight,

(1′) a dw/d log (M) value becomes maximum in a range of 3.4≤log (M)≤4.5,

(2) a ratio of a value obtained by integrating the dw/d log (M) value over a range of 4.00≤log (M)≤4.50 to a value obtained by integrating the dw/d log (M) value over an entire range of the log (M) in the differential molecular weight distribution curve is 6 to 40%, and

(3) a product, of a log (M) value at which the dw/d log (M) value becomes maximum and a percentage (%) of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve, is 20 to 130.

Here, when the value for the log (M) at which the dw/d log (M) value becomes maximum in (1′) is 3.4 or more, sufficient low-temperature impact resistance is obtained, and when the value is 4.5 or less, a satisfactory external appearance is obtained. It is more preferred that, in (1′), the dw/d log (M) value become maximum in the range of 3.5≤log (M)≤4.2.

In (2), when the ratio of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve is 6% or more, sufficient low-temperature impact resistance is obtained, and when the ratio is 40% or less, a satisfactory appearance is obtained. The ratio of the value in (2) is more preferably 6.5 to 30%.

Further, in (3), when the product of, the log (M) value at which the dw/d log (M) value becomes maximum and the percentage (%) of the value obtained by integrating the dw/d log (M) value over the range of 4.00≤log (M)≤4.50 to the value obtained by integrating the dw/d log (M) value over the entire range of the log (M) in the differential molecular weight distribution curve, is 20 or more, sufficient low-temperature impact resistance is obtained, and when the product is 130 or less, a satisfactory appearance is obtained. In (3), the product is more preferably 25 to 125.

A method of regulating the molecular weight distribution of the polyorganosiloxane block (B′) in the polycarbonate-polyorganosiloxane copolymer (E′-1) is, for example, the same method as that in the case of the PC-POS copolymer (E-1) to be used in the polycarbonate-based resin composition according to the first embodiment. In addition to the foregoing, a method involving using a mixture obtained by mixing a plurality of PC-POS copolymers as the (E′-1) is also permitted.

The PC-POS copolymer (E′-1) to be used in the polycarbonate-based resin composition according to the second embodiment of the present invention preferably contains the PC-POS copolymer (E-1) from the viewpoint that the effects of the present invention are obtained.

The structures represented by the general formula (I) and the general formula (II) in the PC-POS copolymer (E′-1) to be used in the polycarbonate-based resin composition according to the second embodiment, raw materials to be used in the production of a PC-POS copolymer in the (E′-1), a method of producing the PC-POS copolymer, and their preferred modes are identical to those of the (E-1) unless otherwise stated.

The average chain length of the polyorganosiloxane block (B′) of the PC-POS copolymer (E′-1) to be used in the polycarbonate-based resin composition of the second embodiment is preferably 30 to 85, more preferably 40 to 75, still more preferably 58 to 72. The average chain length is calculated by nuclear magnetic resonance (NMR) measurement. When the average chain length is 30 or more, impact resistance at low temperature is sufficiently obtained. In addition, when the average chain length n is 85 or less, a copolymer excellent in appearance of molded product can be obtained.

When the PC-POS copolymer (E′-1) is a mixture of a plurality of PC-POS copolymers, the average chain length of the polyorganosiloxane block (B′) can be determined by calculation from the average chain length and content ratio of the POS block of each PC-POS copolymer.

The content of the polyorganosiloxane block (B′) in the PC-POS copolymer (E′-1) is preferably 0.5 to 20.0 mass %, more preferably 1.5 to 15.0 mass %. When the content of the polyorganosiloxane block (B′) is 0.5 mass % or more, sufficient low-temperature impact resistance is obtained, and when the content is 20.0 mass % or less, sufficient heat resistance is obtained.

The viscosity-average molecular weight of the PC-POS copolymer (E′-1) is typically 12,000 to 40,000, preferably 15,000 to 30,000. When the viscosity-average molecular weight is 12,000 or more, the strength of a molded article is sufficient. When the viscosity-average molecular weight is 40,000 or less, injection molding or extrusion molding can be performed in a proper temperature region, and hence a satisfactory appearance is obtained.

The polycarbonate-based resin to be used in the polycarbonate-based resin composition of the second embodiment can contain a homopolycarbonate formed of a repeating unit represented by the general formula (I) or copolymerized polycarbonate, in addition to the PC-POS copolymer (E′-1). The content of the PC-POS copolymer (E′-1) in the polycarbonate-based resin is preferably 10 mass % or more, more preferably 20 mass % or more, still more preferably 40 mass % or more, still further more preferably 50 mass % or more and 100 mass % or less from the viewpoint that the effects of the present invention are obtained.

In the polycarbonate-based resin composition of the second embodiment, the content of the polyorganosiloxane block (B′) containing a repeating unit represented by the general formula (II) in the polycarbonate-based resin is preferably 0.5 to 20.0 mass %, more preferably 1.5 to 15.0 mass %. When the content of the polyorganosiloxane block (B′) is 0.5 mass % or more, sufficient low-temperature impact resistance is obtained, and when the content is 20.0 mass % or less, sufficient heat resistance is obtained.

[White Pigment]

The white pigment is used in the polycarbonate-based resin composition of the present invention. The white pigment is used for making the color tone of the polycarbonate-based resin composition of the present invention white. The white pigment is not particularly limited, but at least one selected from titanium oxide, zinc oxide, talc, barium sulfate, calcium carbonate, and zinc sulfide is preferably used. Among those white pigments, titanium oxide is preferably used from the viewpoint that the color tone is made whiter.

The white pigment is preferably used after its surface has been coated by treating the surface with a surface treatment agent from the viewpoint of suppressing a reduction in impact resistance of the composition. Examples of the surface treatment agent for coating the surface of the white pigment may include: a polyol compound; an amine compound; a hydrous oxide and/or oxide of at least one of metal selected from the group consisting of aluminum, silicon, zirconium, tin, cerium, titanium, and zinc; and a polyorganosiloxane. Among them, at least one selected from the polyol compound, the amine compound, alumina, silica, and the polyorganosiloxane is preferred, and at least one selected from the polyol compound, alumina, silica, and the polyorganosiloxane is more preferred. The white pigment is more preferably titanium oxide coated with at least one selected from the polyol compound, the amine compound, alumina, silica, and the polyorganosiloxane, still more preferably titanium oxide coated with at least one selected from the polyol compound, alumina, silica, and the polyorganosiloxane.

Specific examples of the polyol compound include trimethylolpropane, trimethylolethane, ditrimethylolpropane, trimethylolpropane ethoxylate, and pentaerythritol. Among them, trimethylolpropane and trimethylolethane are preferred.

In addition, when the white pigment is used, a polyorganosiloxane is preferably added to the polycarbonate-based resin composition from the viewpoint of suppressing a reduction in impact-resisting characteristic of the composition.

Specific examples of the polyorganosiloxane include an alkyl hydrogen silicone and an alkoxy silicone. Examples of the alkyl hydrogen silicone include methyl hydrogen silicone and ethyl hydrogen silicone. Examples of the alkoxy silicone include methoxy silicone and ethoxy silicone. A preferred alkoxy silicone is specifically a silicone compound containing an alkoxysilyl group in which an alkoxy group is bonded to a silicon atom directly or through a divalent hydrocarbon group, and examples thereof include linear, cyclic, and network organopolysiloxanes, and a linear organopolysiloxane having a partial branch. Among them, the linear organopolysiloxane is particularly preferred. More specifically, a polyorganosiloxane having a molecular structure in which an alkoxy group is bonded to a silicone main chain through a methylene chain is preferred. As such polyorganosiloxane, for example, commercially available products, such as SH1107, SR2402, BY16-160, BY16-161, BY16-160E, and BY16-161E manufactured by Dow Corning Toray Co., Ltd., may be suitably used.

The white pigment needs to be incorporated in an amount of 0.5 to 5 parts by mass into 100 parts by mass of the polycarbonate-based resin. When the amount of the white pigment is 0.5 part by mass or more, the white pigment exhibits a sufficient effect. When the amount is 5 parts by mass or less, the reduction in impact-resisting characteristic can be sufficiently suppressed. The amount of the white pigment is preferably 1 to 4 parts by mass, more preferably 2 to 4 parts by mass, still more preferably 2 to 3 parts by mass, with respect to 100 parts by mass of the polycarbonate-based resin.

[Antioxidant]

An antioxidant is preferably incorporated into the polycarbonate-based resin composition of the present invention. The incorporation of the antioxidant into the polycarbonate-based resin composition can prevent the oxidative deterioration of the polycarbonate-based resin composition at the time of its melting, and hence can prevent its coloring or the like due to the oxidative deterioration. For example, a phosphorus-based antioxidant and/or a phenol-based antioxidant is suitably used as the antioxidant.

Examples of the phosphorus-based antioxidant include triphenyl phosphite, diphenylnonyl phosphite, diphenyl(2-ethylhexyl) phosphite, tris(2,4-di-t-butylphenyl) phosphite, trisnonylphenyl phosphite, diphenylisooctyl phosphite, 2,2′-methylenebis(4,6-di-t-butylphenyl)octyl phosphite, diphenylisodecyl phosphite, diphenyl mono(tridecyl) phosphite, phenyl diisodecyl phosphite, phenyl di(tridecyl) phosphite, tris(2-ethylhexyl) phosphite, tris(isodecyl) phosphite, tris(tridecyl) phosphite, dibutyl hydrogen phosphite, trilauryl trithiophosphite, tetrakis(2,4-di-t-butylphenyl)-4,4′-biphenylene diphosphonite, 4,4′-isopropylidenediphenol dodecyl phosphite, 4,4′-isopropylidenediphenol tridecyl phosphite, 4,4′-isopropylidenediphenol tetradecyl phosphite, 4,4′-isopropylidenediphenol pentadecyl phosphite, 4,4′-butylidenebis(3-methyl-6-t-butylphenyl)ditridecyl phosphite, bis(2,4-di-t-butylphenyl)pentaerythritol diphosphite, bis(2,6-di-t-butyl-4-methylphenyl)pentaerythritol diphosphite, bis(nonylphenyl)pentaerythritol diphosphite, distearyl-pentaerythritol diphosphite, phenyl bisphenol A pentaerythritol diphosphite, tetraphenyl dipropylene glycol diphosphite, 1,1,3-tris(2-methyl-4-di-tridecyl phosphite-5-t-butylphenyl)butane, 3,4,5,6-dibenzo-1,2-oxaphosphane, triphenylphosphine, diphenylbutylphosphine, diphenyloctadecylphosphine, tris-(p-tolyl)phosphine, tris-(p-nonylphenyl)phosphine, tris-(naphthyl)phosphine, diphenyl-(hydroxymethyl)-phosphine, diphenyl-(acetoxymethyl)-phosphine, diphenyl-ethylcarboxyethyl)-phosphine, tris-(p-chlorophenyl)phosphine, tris-(p-fluorophenyl)phosphine, diphenylbenzylphosphine, diphenyl-β-cyanoethylphosphine, diphenyl-(p-hydroxyphenyl)-phosphine, diphenyl-1,4-dihydroxyphenyl-2-phosphine, and phenylnaphthylbenzylphosphine.

Examples of the phosphorus-based antioxidant may include commercially available products, such as Irgafos 168 (manufactured by BASF Japan, trademark), Irgafos 12 (manufactured by BASF Japan, trademark), Irgafos 38 (manufactured by BASF Japan, trademark), ADK STAB 2112 (manufactured by ADEKA Corporation, trademark), ADK STAB C (manufactured by ADEKA Corporation, trademark), ADK STAB 329K (manufactured by ADEKA Corporation, trademark), ADK STAB PEP36 (manufactured by ADEKA Corporation, trademark), JC-263 (manufactured by Johoku Chemical Co., Ltd., trademark), Sandstab P-EPQ (manufactured by Clariant, trademark), Weston 618 (manufactured by GE, trademark), Weston 619G (manufactured by GE, trademark), and Weston 624 (manufactured by GE, trademark).

Examples of the phenol-based antioxidant include hindered phenols, such as n-octadecyl-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate, 2,6-di-t-butyl-4-methylphenol, 2,2′-methylenebis(4-methyl-6-t-butylphenol), and pentaerythrityl-tetrakis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate].

Among those antioxidants, antioxidants each having a pentaerythritol diphosphite structure, such as bis(2,6-di-tert-butyl-4-methylphenyl)pentaerythritol diphosphite and bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite, and triphenylphosphine are preferred.

Examples of the phenol-based antioxidant may include commercially available products, such as Irganox 1010 (manufactured by BASF Japan, trademark), Irganox 1076 (manufactured by BASF Japan, trademark), Irganox 1330 (manufactured by BASF Japan, trademark), Irganox 3114 (manufactured by BASF Japan, trademark), Irganox 3125 (manufactured by BASF Japan, trademark), BHT (manufactured by Takeda Pharmaceutical Company, trademark), Cyanox 1790 (manufactured by American Cyanamid Company, trademark), and Sumilizer GA-80 (manufactured by Sumitomo Chemical Co., Ltd., trademark).

The content of the antioxidant is about 0.001 to about 0.5 parts by mass, preferably 0.01 to 0.3 parts by mass, more preferably 0.05 to 0.3 parts by mass, with respect to 100 parts by mass of the polycarbonate-based resin. When the content of the antioxidant is 0.001 part by mass or more, a sufficient antioxidant effect is obtained, and when the content is 0.5 part by mass or less, the contamination of a die to be used at the time of the molding of the composition can be sufficiently suppressed.

[UV Absorber]

A UV absorber can be incorporated into the polycarbonate-based resin composition of the present invention as required. Examples of the UV absorber include a benzotriazole-based compound, a benzoxazinone-based compound, a salicylate-based compound, a malonate-based compound, an oxalyl anilide-based compound, a triazine-based compound, a benzophenone-based compound, and a cyanoacrylate-based compound. Those UV absorbers may be used alone or in combination thereof.

Specific examples of the benzotriazole-based compound may include 2-(2′-hydroxy-5′-tert-octylphenyl)benzotriazole, 2-(2′-hydroxy-3′,5′-di-tert-amylphenyl)benzotriazole, 2-(2′-hydroxy-5′-tert-butylphenyl)benzotriazole, 2-(2′-hydroxy-3′,5′-di-tert-butylphenyl)benzotriazole, 2-[2′-hydroxy-3′,5′-bis(α,α-dimethylbenzyl)phenyl]-2H-benzotriazole, and 2,2′-methylene-bis[4-methyl-6-(benzotriazol-2-yl)phenol].

Specific examples of the triazine-based compound may include 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxy-phenol and 2-(4,6-bis-2,4-dimethylphenyl-1,3,5-triazin-2-yl)-5-(hexyl)oxy-phenol.

Specific examples of the benzophenone-based compound may include 2-hydroxy-4-n-octoxybenzophenone, 2-hydroxy-4-methoxy-benzophenone, and 2-hydroxy-4-ethoxy-benzophenone.

Specific examples of the cyanoacrylate-based compound may include 2-ethyl-2-cyano-3,3-diphenylacrylate, 2-ethylhexyl-2-cyano-3,3-diphenylacrylate and 1,3-bis-[2′-cyano-3,3′-diphenylacryloyloxy]-2,2-bis-[(2-cyano-3′,3′-diphenylacryloyl) oxy]methylpropane.

Among them, at least one selected from the group consisting of a benzotriazole-based compound and a triazine-based compound is preferred.

Examples of the UV absorber may include commercially available products, such as SEESORB 709 (ShiproKaseiKaisha, Ltd., trademark), ChemiSorb 79 (Chemipro Kasei Kaisha, Ltd., trademark), Hostavin B-CAP (manufactured by Clariant, trademark), Tinuvin 1577 (manufactured by BASF Japan, trademark), and Cyasorb UV-3638 (manufactured by Cytec Technology Corporation).

The content of the UV absorber is about 0.01 to about 1.0 part by mass, preferably 0.05 to 0.7 parts by mass, more preferably 0.1 part to 0.5 parts by mass, with respect to 100 parts by mass of the polycarbonate-based resin. When the content of the UV absorber is 0.01 part by mass or more, a sufficient light-resisting characteristic is obtained, and when the content is 1.0 part by mass or less, the contamination of the die to be used at the time of the molding can be sufficiently suppressed.

Any other additive can be incorporated into the polycarbonate-based resin composition of the present invention to the extent that the effects of the present invention are not impaired. Examples of the other additive may include a flame retardant, a flame retardant aid, a release agent, a reinforcing material, a filler, an elastomer for improving impact resistance, and a dye.

The polycarbonate-based resin composition according to the second embodiment of the present invention needs to have an Izod impact strength at −40° C. of 30 kJ/m²or more, and is hence excellent in low-temperature impact resistance. The Izod impact strength can be measured as follows: a test piece is produced by making a notch in a test piece having a thickness of 3.2 mm (about ⅛ inch), which has been obtained by using the polycarbonate-based resin composition, through a post-treatment, and its Izod impact strength is measured in conformity with ASTM Standard D-256. Specifically, the Izod impact strength can be measured by a method described in Examples. The Izod impact strength at −40° C. is preferably 40 kJ/m²or more.

The polycarbonate-based resin composition of the present invention is obtained by: blending the above-mentioned respective components at the above-mentioned ratios and various optional components to be used as required at appropriate ratios; and kneading the components.

The blending and the kneading may be performed by a method involving premixing with a typically used apparatus, such as a ribbon blender or a drum tumbler, and using, for example, a Henschel mixer, a Banbury mixer, a single-screw extruder, a twin-screw extruder, a multi-screw extruder, or a Ko-kneader. In normal cases, a heating temperature at the time of the kneading is appropriately selected from the range of 240 to 320° C. An extruder, in particular a vented extruder is preferably used as the melt-kneading molding machine.

[Molded Article]

A molded article of the present invention comprises the polycarbonate-based resin composition of the present invention. Various molded articles can be produced by using the polycarbonate-based resin composition of the present invention through molding with the melt-kneading molding machine, or by using a pellet obtained from the composition as a raw material through molding by an injection molding method, an injection compression molding method, an extrusion molding method, a blow molding method, a press molding method, a vacuum molding method, an foam molding method, and the like. In particular, the resultant pellet can be suitably used in the production of injection-molded articles by injection molding and injection compression molding.

The molded article comprising the polycarbonate-based resin composition of the present invention can be suitably used as, for example,

(1) a part for electrical and electronic equipment, such as a television, a radio-cassette player, a video camera, a videotape recorder, an audio player, a DVD player, an air conditioner, a cellular phone, a display, a computer, a register, an electronic calculator, a copying machine, a printer, or a facsimile, or

(2) a casing for the electrical and electronic equipment described in the (1).

EXAMPLES

The present invention is more specifically described by way of Examples. However, the present invention is by no means limited by these Examples. In each of Examples, characteristic values and evaluation results were determined in the following manner.

(1) Gel Permeation Chromatography (GPC)

The GPC measurement of the polyorganosiloxane was carried out under the following conditions.

Test apparatus: TOSOH HLC 8220

Column: TOSOH TSK-GEL GHXL-L, G4000HXL, G2000HXL

Solvent: tetrahydrofuran (THF)

Column temperature: 40° C.

Flow rate: 1.0 ml/min

Detector: RI

Injection concentration: 0.2 w/v %

Injection amount: 0.1 ml

Standard polystyrene manufactured by Tosoh Corporation was used to obtain a calibration curve.

A differential molecular weight distribution curve can be obtained by such method as described below. First, the time curve of an intensity distribution detected with a RI detector (elution curve) was converted into a molecular weight distribution curve with respect to the logarithmic value of a molecular weight (log (M)) by using a calibration curve. Next, an integral molecular weight distribution curve with respect to the log (M) when the total area of the distribution curve was set to 100% was obtained. After that, a differential molecular weight distribution curve with respect to the log (M) can be obtained by differentiating the integral molecular weight distribution curve with respect to the log (M). It should be noted that a series of operations up to the acquisition of the differential molecular weight distribution curve can be typically performed with analysis software built in a GPC measuring apparatus. FIG. 1 is a graph for showing an example of the differential molecular weight distribution curve to be obtained. In the graph, the log (M) value at which a dw/d log (M) value becomes maximum is shown and a value obtained by integrating dw/d log (M) over the range of 4.00≤log (M)≤4.50 is shown in a shaded area.

The GPC measurement of the polyorganosiloxane block (B) in the polycarbonate-polyorganosiloxane copolymer (E-1) was performed under the following conditions.

20 ml of methylene chloride was added to 4.3 g of the resultant PC-POS copolymer flake to completely dissolve the flake. While the solution was stirred with a magnetic stirrer, 20 ml of a solution of sodium hydroxide in methanol (obtained by mixing 48 mass % aqueous NaOH and methanol at a volume ratio of 1:9) was added to the solution, followed by stirring for 30 minutes. In order for a precipitated solid crystal derived from a PC to be dissolved, 25 ml of ion-exchanged water was added to the mixture, and the whole was stirred for 1 minute and then left at rest to be separated into an organic layer and an aqueous layer. Thus, the organic layer was obtained. The organic layer was washed by adding 15 vol % of 0.03 mol/L aqueous NaOH with respect to the organic layer to the organic layer and stirring the mixture, and then the mixture was subjected to settled separation to provide an organic layer; the foregoing operation was performed twice. The resultant organic layer was washed by adding 15 vol % of 0.2 mol/L hydrochloric acid with respect to the organic layer to the organic layer and stirring the mixture, and then the mixture was subjected to settled separation to provide an organic layer. Next, the organic layer was washed by adding 15 vol % of pure water with respect to the organic layer to the organic layer and stirring the mixture, and then the mixture was subjected to settled separation to provide an organic layer. The resultant organic layer was dried with a dryer at 60° C. for 16 hours. The spectrum of the resultant sample was measured by GPC. Here, it is found from the resultant GPC spectrum that when a molecular weight in terms of polystyrene is represented by M, the sample is formed of a low-molecular weight component derived from the PC having the maximum value at a log (M) of 2.0 or more to less than 3.0, and a POS component having the maximum value at a log (M) of 3.0 or more to less than 4.5. The molecular weight distribution of the used polyorganosiloxane can be identified by identifying the spectrum of the POS.

In addition, the GPC measurement of the polyorganosiloxane block (B′) in the polycarbonate-polyorganosiloxane copolymer (E′-1) was performed under the same conditions except that “4.3 g of the PC-POS copolymer flake” was changed to “4.3 g of a pellet of a resin composition obtained in each example.”

(2) Chain Length and Content of Polydimethylsiloxane

The chain length and content of a polydimethylsiloxane were calculated by NMR measurement from the integrated value ratio of a methyl group of the polydimethylsiloxane.

<Quantification Method for Chain Length of Polydimethylsiloxane>
¹H-NMR Measurement Conditions

NMR apparatus: ECA500 manufactured by JEOL Resonance Co., Ltd.

Probe: 50TH5AT/FG2

Observed range: −5 to 15 ppm

Observation center: 5 ppm

Pulse repetition time: 9 sec

Pulse width: 45°

NMR sample tube: 5φ

Sample amount: 45 to 55 mg

Solvent: deuterochloroform

Measurement temperature: room temperature

Number of scans: 256 times

In the Case of Allylphenol-terminated Polydimethylsiloxane

A: an integrated value of a methyl group in a dimethylsiloxane moiety observed around δ−0.02 to δ 0.5

B: an integrated value of a methylene group in allylphenol observed around δ 2.50 to δ 2.75

Chain length of polydimethylsiloxane=(A/6)/(B/4)

In the Case of Eugenol-terminated Polydimethylsiloxane

A: an integrated value of a methyl group in a dimethylsiloxane moiety observed around δ−0.02 to δ 0.5

B: an integrated value of a methylene group in eugenol observed around δ 2.40 to δ 2.70

Chain length of polydimethylsiloxane=(A/6)/(B/4)

Quantification Method for Copolymerization Amount of Polydimethylsiloxane in p-t-Butylphenol (PTBP)-terminated Polycarbonate obtained by copolymerizing Allylphenol-terminated Polydimethylsiloxane

NMR apparatus: ECA-500 manufactured by JEOL Resonance Co., Ltd.

Probe: TH5 corresponding to 5 cp NMR sample tube

Observed range: −5 to 15 ppm

Observation center: 5 ppm

Pulse repetition time: 9 sec

Pulse width: 45°

Number of scans: 256 times

NMR sample tube: 5φ

Solvent: deuterochloroform

Measurement temperature: room temperature

A: an integrated value of a methyl group in a BPA moiety observed around δ 1.5 to 1.9

B: an integrated value of a methyl group in a dimethylsiloxane moiety observed around δ−0.02 to 0.3

C: an integrated value of a butyl group in a p-tert-butylphenyl moiety observed around δ 1.2 to 1.4

a=A/6

b=B/6

c=C/9

T=a+b+c

f=a/T×100

g=b/T×100

h=c/T×100

TW=f×254+g×74.1+h×149

PDMS (wt %)=g×74.1/TW×100

(3) Viscosity-Average Molecular Weight

A viscosity-average molecular weight (Mv) was calculated from the following equation (Schnell's equation) by using a limiting viscosity [η] determined through the measurement of the viscosity of a methylene chloride solution at 20° C. with an Ubbelohde-type viscometer.

[η]=1.23×10⁻⁵×Mv^0.83

To 5.6 mass % aqueous sodium hydroxide, 2,000 ppm of sodium dithionite with respect to bisphenol A (BPA) (to be dissolved later) was added. BPA was dissolved in the solution so that the concentration of BPA became 13.5 mass %. Thus, a solution of BPA in aqueous sodium hydroxide was prepared. The solution of BPA in aqueous sodium hydroxide, methylene chloride, and phosgene were continuously passed through a tubular reactor having an inner diameter of 6 mm and a tube length of 30 m at flow rates of 40 L/hr, 15 L/hr, and 4.0 kg/hr, respectively. The tubular reactor had a jacket portion and the temperature of a reaction liquid was kept at 40° C. or less by passing cooling water through the jacket. The reaction liquid that had exited the tubular reactor was continuously introduced into a baffled vessel-type reactor having an internal volume of 40 L provided with a sweptback blade, and then the solution of BPA in aqueous sodium hydroxide, 25 mass % aqueous sodium hydroxide, water, and a 1 mass % aqueous solution of triethylamine were further added to the reactor at flow rates of 2.8 L/hr, 0.07 L/hr, 17 L/hr, and 0.64 L/hr, respectively, to thereby perform a reaction. The reaction liquid flowing out of the vessel-type reactor was continuously taken out, and then an aqueous phase was separated and removed by leaving the liquid at rest, followed by the collection of a methylene chloride phase.

The concentration of the polycarbonate oligomer thus obtained was 330 g/L and the concentration of a chloroformate group thereof was 0.71 mol/L.

<Production of PC-POS Copolymer (E-1)>
Production Example 1 (Production of SiPC-a1)

14 L of the polycarbonate oligomer solution produced as described above, 11.9 L of methylene chloride, a solution obtained by dissolving 264 g of an allylphenol terminal-modified polydimethylsiloxane (a polydimethylsiloxane is hereinafter sometimes referred to as “PDMS”) having an average chain length n of 64, a log (M) at which dw/d log (M) became the maximum value of 3.7, and a ratio of a value obtained by integrating the dw/d log (M) value over the log (M) range of 4.00 to 4.50 to a value obtained by integrating the dw/d log (M) value over the entire range of the log (M) (hereinafter, in Examples, the ratio is sometimes referred to as “ratio of a log (M) of 4.00 to 4.50”) of 15.0% in 800 ml of methylene chloride, and 7.9 mL of triethylamine were loaded into a 50-liter vessel-type reactor including a baffle board, a paddle-type stirring blade, and a cooling jacket. 1,388 g of 6.4 mass % aqueous sodium hydroxide was added to the mixture under stirring, and a reaction between the polycarbonate oligomer and the allylphenol terminal-modified PDMS was performed for 20 minutes. The allylphenol terminal-modified PDMS used here is obtained by blending, at a mass ratio of 5:5, an allylphenol terminal-modified PDMS having an average chain length n of 34, a log (M) at which dw/d log (M) becomes the maximum value of 3.6, and a ratio of a log (M) of 4.00 to 4.50 of 5.6%, and an allylphenol terminal-modified PDMS having an average chain length n of 92, a log (M) at which dw/d log (M) becomes the maximum value of 4.1, and a ratio of a log (M) of 4.00 to 4.50 of 34.8%.

A solution of p-t-butylphenol (PTBP) in methylene chloride (prepared by dissolving 132.9 g of PTBP in 1.3 L of methylene chloride) and a solution of BPA in aqueous sodium hydroxide (prepared by dissolving 997 g of BPA in an aqueous solution prepared by dissolving 588 g of NaOH and 2.0 g of sodium dithionite in 8.6 L of water) were added to the polymerization liquid, and the mixture was subjected to a polymerization reaction for 40 minutes.

10 L of methylene chloride was added to the resultant for dilution, and the mixture was stirred for 20 minutes. After that, the mixture was separated into an organic phase containing a PC-PDMS, and an aqueous phase containing excess amounts of BPA and NaOH, and the organic phase was isolated.

A solution of the PC-PDMS in methylene chloride thus obtained was sequentially washed with 0.03 mol/L aqueous NaOH and 0.2 N hydrochloric acid in amounts of 15 vol % each with respect to the solution. Next, the solution was repeatedly washed with pure water until an electric conductivity in an aqueous phase after the washing became 0.01 μS/m or less.

A solution of the polycarbonate in methylene chloride obtained by the washing was concentrated and pulverized, and the resultant flake was dried under reduced pressure at 120° C. The flake had a PDMS concentration of 4.8 mass %, a viscosity number measured in conformity with ISO 1628-4 (1999) of 47.4, and a viscosity-average molecular weight Mv of 17,700. Thus, an SiPC-a1 was obtained as the PC-POS (E-1). The characteristic values of the resultant SiPC-a1 are shown in Table 1.

Production Example 2 (Production of SiPC-a2)

In Production Example 1, the amount of the allylphenol terminal-modified polydimethylsiloxane (PDMS) was changed to 350 g. The resultant SiPC-a2 had a PDMS concentration of 6.0 mass %, a viscosity number measured in conformity with ISO 1628-4 (1999) of 47.4, and a viscosity-average molecular weight Mv of 17,700.

Production Example 3 (Production of SiPC-a3)

In Production Example 1, 264 g of the allylphenol terminal-modified polydimethylsiloxane was changed to 350 g of a eugenol terminal-modified polydimethylsiloxane (PDMS) having an average chain length n of 63, a log (M) at which dw/d log (M) became the maximum value of 3.8, and a ratio of a log (M) of from 4.00 to 4.50 of 15.1%. The resultant SiPC-a3 had a PDMS concentration of 6.0 mass %, a viscosity number measured in conformity with ISO 1628-4 (1999) of 47.4, and a viscosity-average molecular weight Mv of 17,700. The eugenol terminal-modified PDMS used here is obtained by blending, at a mass ratio of 5:5, a eugenol terminal-modified PDMS having an average chain length n of 35, a log (M) at which dw/d log (M) becomes the maximum value of 3.6, and a ratio of a log (M) of 4.00 to 4.50 of 5.6%, and a eugenol terminal-modified PDMS having an average chain length n of 91, a log (M) at which dw/d log (M) becomes the maximum value of 4.1, and a ratio of a log (M) of 4.00 to 4.50 of 34.5%.

<Production of PC-POS Copolymer Except PC-POS Copolymer (E-1)>
Production Example 4 (Production of SiPC-b1)

A flake of a PC-POS copolymer (SiPC-b1) was obtained in the same manner as in Production Example 1 except that the allylphenol terminal-modified PDMS used in Production Example 1 was changed to 350 g of an allylphenol terminal-modified PDMS having an average chain length n of 92, a log (M) at which dw/d log (M) took the maximum value of 4.1, and a ratio of a log (M) of 4.00 to 4.50 of 34.8%. The resultant flake had a PDMS amount of 6.0 mass %, a viscosity number measured in conformity with ISO 1628-4 (1999) of 47.4, and a viscosity-average molecular weight of 17,700. The characteristic values of the resultant SiPC-b1 are shown in Table 1.

Production Example 5 (Production of SiPC-c1)

A flake of a PC-POS copolymer (SiPC-c1) was obtained in the same manner as in Production Example 1 except that the allylphenol terminal-modified PDMS used in Production Example 1 was changed to an allylphenol terminal-modified PDMS having an average chain length n of 34, a log (M) at which dw/d log (M) took the maximum value of 3.6, and a ratio of a log (M) of 4.00 to 4.50 of 5.6%. The resultant flake had a PDMS amount of 5.9 mass %, a viscosity number measured in conformity with ISO 1628-4 (1999) of 47.3, and a viscosity-average molecular weight of 17,500. The characteristic values of the resultant SiPC-c1 are shown in Table 1.

TABLE 1

Production Examples

1
2
3
4
5

SiPC-a1
SiPC-a2
SiPC-a3
SiPC-b1
SiPC-c1

Average chain length (n)

64
64
65
92
34

(1) log(M) at which dw/dlog(M)

3.8
3.8
3.8
4.1
3.6

becomes maximum

(2) Ratio of log(M) of
%
18.4
18.4
18.5
34.5
5.4

from 4.00 to 4.50

PDMS content
mass %
4.8
6.0
6.0
6.0
5.9

Viscosity number (V/N)

47.4
47.4
47.4
47.4
47.3

Viscosity-average molecular

17,700
17,700
17,700
17,700
17,500

weight (Mv)

Examples 1 to 16 and Comparative Examples 1 to 7

Any one of the PC-POS copolymers obtained in Production Examples 1 to 5 and other respective components were mixed at a blending ratio (unit; parts by mass) shown in Table 2 or Table 3, and the mixture was supplied to a vented twin-screw extruder (manufactured by Toshiba Machine Co., Ltd., TEM-35B) and melt-kneaded at a screw revolution number of 150 rpm, an ejection amount of 20 kg/hr, and a resin temperature of from 295° C. to 300° C. to provide an evaluation pellet sample. The evaluation pellet sample was dried at 120° C. for 8 hours, and was then subjected to injection molding with an injection molding machine (manufactured by Nissei Plastic Industrial Co., Ltd., NEX110, screw diameter: 36 mmϕ) at a cylinder temperature of 280° C. and a die temperature of 80° C. to produce a test piece for performing each test (a test piece size is described below). In addition, the other respective components are described below. The respective components and the results of evaluation tests are shown in Table 2 and Table 3.

(Test Piece Size)

Molded article weight (sprue+runner (8 mmϕ)+test piece): 49 g

Test pieces: two Izod test pieces each measuring 63 mm by 13 mm by 3.2 mm, a HDT test piece measuring 126 mm by 13 mm by 3.2 mm, a flat test piece measuring 34 mm by 25 mm by 3.2 mm, a tensile test piece measuring 173 mm in length by 10 mm in width in a parallel portion by 3.2 mm in thickness, and a bending test piece measuring 99 mm by 10 mm by 4.0 mm.

[Evaluation Test]
<Izod Impact Strength>

Notched Izod impact strengths at measurement temperatures of 23° C. and −40° C. were measured by using a test piece, which had been obtained by making a notch in a test piece having a thickness of 3.2 mm (about ⅛ inch) produced with an injection molding machine through a post-treatment, in conformity with ASTM Standard D-256. Judgment criteria for the notched Izod impact strengths are as follows: a notched Izod impact strength at 23° C. of 60 kJ/m²or more means that impact resistance at 23° C. is excellent, and a notched Izod impact strength at −40° C. of 30 kJ/m²or more means that impact resistance at low temperature is excellent.

The amount (×10²mL/sec) of a molten resin flowing out of a nozzle having a diameter of 1 mm and a length of 10 mm was measured with a Koka flow tester in conformity with JIS K 7210 at 280° C. under a pressure of 15.7 MPa. A higher Q value means that a resin composition is more excellent in flowability.

A vertical flame test was performed with a test piece (measuring 127 mm long by 12.7 mm wide by 1.5 mm thick) produced in conformity with UL Standard 94. UL Standard 94 is a method of evaluating flame retardancy from an after flame time after the flame of a burner has been brought into contact with a test piece having a predetermined size, which has been vertically held, for 10 seconds.

The HDT of a test piece was measured in conformity with ASTM D648 at a load of 1.83 MPa. The HDT serves as a guideline on heat resistance, and a judgment criterion therefor is as follows: a HDT of 120° C. or more means that the test piece has sufficient heat resistance.

The surface appearance of the molded article for a tensile test was visually observed and evaluated in accordance with the following evaluation criteria.

A: No brown to black streak is observed on the surface of the molded article.

C: A brown to black streak is observed on the surface of the molded article.

[Other Components]
<Aromatic Polycarbonate Resin>

PC-1: aromatic homopolycarbonate resin [manufactured by Idemitsu Kosan Co., Ltd., TARFLON FN1700 (product name), viscosity-average molecular weight=17,700]

PC-2: aromatic homopolycarbonate resin [manufactured by Idemitsu Kosan Co., Ltd., TARFLON FN1900 (product name), viscosity-average molecular weight=19,300]

PC-3: aromatic homopolycarbonate resin [manufactured by Idemitsu Kosan Co., Ltd., TARFLON FN2200 (product name), viscosity-average molecular weight=21,300]

PC-4: aromatic homopolycarbonate resin [manufactured by Idemitsu Kosan Co., Ltd., TARFLON FN2500 (product name), viscosity-average molecular weight=23,500]

CR63: titanium dioxide [manufactured by Ishihara Sangyo Kaisha, Ltd., titanium dioxide subjected to surface treatment with 1% of silica-alumina and 0.5% of dimethyl silicone, average particle diameter: 0.21 μm]

CR-60-2: titanium dioxide [manufactured by Ishihara Sangyo Kaisha, Ltd., titanium oxide coated with polyol, average particle diameter: 0.21 μm]

PC3: titanium dioxide [manufactured by Ishihara Sangyo Kaisha, Ltd., rutile type titanium dioxide, surface acid amount: 10 μmol/g, surface base amount: 4 μmol/g]

ZnS: zinc sulfide powder [manufactured by Sachtleben Chemie GmbH, average particle diameter: 0.3 μm]

Flame retardant aid: “Metablen A-3800 (product name)” [modified polytetrafluoroethylene (modified PTFE), manufactured by Mitsubishi Rayon Co., Ltd.]

Flame retardant: “EFTOP KFBS (product name)” (potassium perfluorobutane sulfonate, manufactured by Mitsubishi Materials Electronic Chemicals Co., Ltd.)

Antioxidant: “IRGAFOS 168 (product name)”

[tris(2,4-di-t-butylphenyl)phosphite, manufactured by BASF Japan] UV absorber: “SEESORB 709 (product name)”

[2-(2′-hydroxy-5′-t-octylphenyl)benzotriazole, manufactured by Shipro Kasei Kaisha, Ltd.]

TABLE 2

Examples

Blended component (parts by mass)
1
2
3
4
5
6
7
8

PC-based
SiPC (E-1)
SiPC-a1
100
100
100

resin

SiPC-a2

100
100
80
60
40

SiPC-a3

Other SiPC-1
SiPC-b1

40

Homo PC
PC-1

10

PC-2

10

PC-3

PC-4

60

Other SiPC-2
SiPC-c1

White pigment
CR63
2
1
4
2

2
2
2

CR-60-2

PC3

ZnS

1

PTFE
A3800

Flame retardant
KFBS

Antioxidant
Irgafos 168
0.1
0.1
0.1
0.1
0.1
0.1
0.1
0.1

UV absorber
SEESORB

709

Average chain length n of (B′)
64
64
64
64
64
64
75
64

Viscosity-average molecular weight of (E′-1)
17,700
17,700
17,700
17,700
17,700
17,860
17,700
21,180

Content of (B′) in (E′-1)
mass %
4.8
4.8
4.8
6.0
6.0
6.0
6.0
6.0

Analysis
(1)′ Log(M)

3.7
3.7
3.7
3.7
3.7
3.7
3.8
3.7

evaluation
at which dw/dlog(M)

result
becomes maximum

(2) Ratio of Log(M) of
%
15.1
15.1
15.0
15.1
15.1
15.0
26.5
14.9

from 4.00 to 4.50

(3) {(1) × (2)}

55.9
55.9
55.5
55.9
55.9
55.5
100.7
55.1

Amount of PDMS in
mass %
4.8
4.8
4.8
6
6
4.8
6
2.4

PC-based resin

Izod impact strength
23° C.
73
71
67
66
66
73
69
79

(kJ/m²)
−40° C.
51
55
49
51
51
51
57
58

Flowability (Q value) × 0.01 ml/sec
11
11
11
11
11
11
11
6

Flame retardancy

HDT (1.83 MPa) ° C.
126
126
126
125
125
126
125
128

Molded article external
A
A
A
A
A
A
A
A

appearance

Examples

Blended component (parts by mass)
9
10
11
12
13
14
15
16

PC-based
SiPC (E-1)
SiPC-a1

resin

SiPC-a2
25
40
45
45
45

80
40

SiPC-a3

45

Other SiPC-1
SiPC-b1
40
25
20
20
20
20

40

Homo PC
PC-1
22
22
22
22
22
22

PC-2
13
13
13
13
13
13

PC-3

20
20

PC-4

Other SiPC-2
SiPC-c1

White pigment
CR63
2
2
2

2
2
2

CR-60-2

2

PC3

2

ZnS

PTFE
A3800

0.3
0.3

Flame retardant
KFBS

0.05
0.05

Antioxidant
Irgafos 168
0.1
0.1
0.1
0.1
0.1
0.1
0.1
0.1

UV absorber
SEESORB

0.3

709

Average chain length n of (B′)
81
75
73
73
73
73
64
78

Viscosity-average molecular weight of (E′-1)
17,908
17,908
17,908
17,908
17,908
17,908
18,420
18,420

Content of (B′) in (E′-1)
mass %
6.0
6.0
6.0
6.0
6.0
6.0
6.0
6.0

Analysis
(1)′ Log(M)

4.1
3.8
3.8
3.8
3.8
3.8
3.7
3.8

evaluation
at which dw/dlog(M)

result
becomes maximum

(2) Ratio of Log(M) of
%
29.6
26.6
25.1
25.1
25.0
25.2
14.9
28.1

from 4.00 to 4.50

(3) {(1) × (2)}

121.4
101.1
95.4
95.4
95.0
95.8
55.1
106.8

Amount of PDMS in
mass %
3.9
3.9
3.9
3.9
3.9
3.9
4.8
4.8

PC-based resin

Izod impact strength
23° C.
68
70
70
70
69
70
74
76

(kJ/m²)
−40° C.
50
46
43
42
43
43
55
57

Flowability (Q value) × 0.01 ml/sec
14
15
15
15
15
15
10
10

Flame retardancy

V-0
V-0

HDT (1.83 MPa) ° C.
126
126
125
125
125
125
126
126

Molded article external
A
A
A
A
A
A
A
A

appearance

TABLE 3

Comparative Examples

Blended component (parts by mass)
1
2
3
4
5
6
7

PC-based resin
SiPC (E-1)
SiPC-a1

SiPC-a2

SiPC-a3

Other SiPC-1
SiPC-b1

100
65
20
25

Homo PC
PC-1

22
22
22
22

PC-2

13
13
13
13

PC-3

PC-4

60

Other SiPC-2
SiPC-c1
100
40

45
40
65

White pigment
CR63
2
2
2
2
2
2
2

CR-60-2

PC3

ZnS

PTFE
A3800

Flame retardant
KFBS

Antioxidant
Irgafos 168
0.1
0.1
0.1
0.1
0.1
0.1
0.1

UV absorber
SEESORB 709

Average chain length n of (B′)
34
34
92
92
52
56
34

Viscosity-average molecular weight of (E′-1)
17,500
21,100
17,700
17,908
17,818
17,828
17,778

Content of (B′) in (E′-1)
mass %
5.9
5.9
6.0
6.0
5.9
5.9
5.9

Analysis
(1)′ Log(M) at which

3.6
3.6
4.1
4.1
3.7
3.7
3.6

evaluation result
dw/dlog(M) becomes

maximum

(2) Ratio of Log(M) of from
%
5.5
5.5
36.0
35.9
14.3
17.3
5.4

4.00 to 4.50

(3) {(1) × (2)}

19.8
19.8
147.6
147.2
52.9
64.0
19.4

Amount of PDMS in
mass %
6
2.4
6
3.9
3.9
3.9
0

PC-based resin

Izod impact strength (kJ/m²)
23° C.
66
78
67
71
71
70
65

−40° C.
25
20
52
53
25
27
20

Flowability (Q value) × 0.01 ml/sec
10
6
11
15
14
15
14

Flame retardancy

HDT (1.83 MPa) ° C.
121
127
125
127
124
125
122

Molded article external appearance
A
A
C
C
A
A
A

As is apparent from Table 2, each of the molded articles obtained from the polycarbonate-based resin compositions of Examples 1 to 16 is excellent in impact resistance, in particular impact resistance at low temperature, and is also excellent in heat resistance and appearance of molded article. Meanwhile, as shown in each of Comparative Examples 1 to 7, when a polycarbonate-based resin containing a specific polycarbonate-polyorganosiloxane copolymer in which the molecular weight distribution of a polyorganosiloxane has been controlled is not used, an excellent molded article that achieves both impact resistance, in particular impact resistance at low temperature and an appearance of molded article is not obtained.

INDUSTRIAL APPLICABILITY

The polycarbonate-based resin composition obtained in the present invention can be suitably used in parts for electrical and electronic equipment, parts for the interior and exterior of lighting equipment, parts for the interior and exterior of a vehicle, food trays, and eating utensils because the composition is excellent in molding external appearance and impact resistance.