Provided is a copolycarbonate comprising a first repeating unit of Chemical Formula 1, a second repeating unit of Chemical Formula 2, and a terminal capping group of Chemical Formula 3:

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Also provided are a method of preparing the copolycarbonate and a molded article including the copolycarbonate.

Provided is a copolycarbonate comprising a first repeating unit of Chemical Formula 1, a second repeating unit of Chemical Formula 2, and a terminal capping group of Chemical Formula 3:

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Also provided are a method of preparing the copolycarbonate and a molded article including the copolycarbonate.

A sheet formed from carbon fiber reinforced thermoplastic resin with high moldability, and a production method of said resin is provided. This sheet is formed from a carbon fiber reinforced thermoplastic resin that contains carbon fibers, dichloromethane, and a thermoplastic resin containing at least one of a polycarbonate resin and a polyarylate resin. The aforementioned at least one of a polycarbonate resin and a polyarylate resin has a terminal structure derived from a monohydric phenol represented by formula (1) and a constituent unit derived from a dihydric phenol, and the content of the dichloromethane contained in the sheet is 10-10,000 ppm by mass. (In formula (1), R.sub.1 represents an alkyl group with 8-36 carbons, or an alkenyl group with 8-36 carbons, and R.sub.2-R.sub.5 independently represent a hydrogen, a halogen, an alkyl group with 1-20 carbons optionally having a substituent, or an aryl group with 6-12 carbons optionally having a substituent.)

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A composition includes a polycarbonate resin formed via an interfacial polymerization process and from 0.05 ppm to 50 ppm of a sulfonic acid. A molded article formed from the composition may exhibit a yellowness index that is less than that of a reference molded article formed from substantially similar polycarbonate composition comprising the polycarbonate resin but in the absence of the sulfonic acid. Methods for forming the molded article in accordance with the above are also described.

A composition includes a polycarbonate resin formed via an interfacial polymerization process and from 0.05 ppm to 50 ppm of a sulfonic acid. A molded article formed from the composition may exhibit a yellowness index that is less than that of a reference molded article formed from substantially similar polycarbonate composition comprising the polycarbonate resin but in the absence of the sulfonic acid. Methods for forming the molded article in accordance with the above are also described.

A polycarbonate resin composition, a molded article, a polycarbonate resin, and an end-capping agent for polycarbonate resins are provided. The polycarbonate resin composition contains: a polycarbonate resin having a terminal structure represented by Formula (A) and having a viscosity average molecular weight from 110.sup.4 to 510.sup.4, and a stabilizer. In Formula (A), R.sup.1 is selected from the group consisting of a hydrogen atom, halogen atoms, linear alkyl groups having from 1 to 9 carbons, branched alkyl groups having from 3 to 9 carbons, linear alkenyl groups having from 2 to 9 carbons, branched alkenyl groups having from 3 to 9 carbons, and aryl groups having from 6 to 12 carbons; and R.sup.2 to R.sup.7 are each independently selected from the group consisting of a hydrogen atom, alkyl groups having from 1 to 9 carbons, and alkoxy groups having from 1 to 9 carbons.

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The present invention relates to an aromatic polycarbonate obtained via the melt transesterification of a diaryl carbonate, a bisphenol and an endcapping agent selected from paracumyl phenol, dicumyl phenol, p-tert-butyl phenol and mixtures of at least two of said endcapping agents, said polycarbonate having a melt volume rate of at least 20 cm.sup.3/10 min (ISO 1133, 300 C., 1.2 kg), a terminal hydroxyl group content of at most 800 ppm by weight, a Fries branching content of at most 1300 ppm by weight and a content of bulky end groups of at least 20 mol % defined as the sum of the mol % of end-groups based on said bisphenol and the mol % of end-groups based on said endcapping agent.

The present invention relates to an aromatic polycarbonate obtained via the melt transesterification of a diaryl carbonate, a bisphenol and an endcapping agent selected from paracumyl phenol, dicumyl phenol, p-tert-butyl phenol and mixtures of at least two of said endcapping agents, said polycarbonate having a melt volume rate of at least 20 cm.sup.3/10 min (ISO 1133, 300 C., 1.2 kg), a terminal hydroxyl group content of at most 800 ppm by weight, a Fries branching content of at most 1300 ppm by weight and a content of bulky end groups of at least 20 mol % defined as the sum of the mol % of end-groups based on said bisphenol and the mol % of end-groups based on said endcapping agent.

Provided is a polycarbonate-polyorganosiloxane copolymer including polycarbonate blocks (A-1) each formed of a specific repeating unit and polyorganosiloxane blocks (A-2) each containing a specific repeating unit, wherein the polycarbonate-polyorganosiloxane copolymer satisfies the following expression (F1a):

15wM1(F1a)

wherein wM1 represents the average content of the polyorganosiloxane blocks (A-2) in polycarbonate-polyorganosiloxane copolymers each having a molecular weight determined by using a polycarbonate as a conversion reference of from 56,000 or more to 200,000 or less among polycarbonate-polyorganosiloxane copolymers obtained through the separation of the polycarbonate-polyorganosiloxane copolymer by gel permeation chromatography.

Provided is a polycarbonate-polyorganosiloxane copolymer including polycarbonate blocks (A-1) each formed of a specific repeating unit and polyorganosiloxane blocks (A-2) each containing a specific repeating unit, wherein the polycarbonate-polyorganosiloxane copolymer satisfies the following expression (F1a):

15wM1(F1a)

wherein wM1 represents the average content of the polyorganosiloxane blocks (A-2) in polycarbonate-polyorganosiloxane copolymers each having a molecular weight determined by using a polycarbonate as a conversion reference of from 56,000 or more to 200,000 or less among polycarbonate-polyorganosiloxane copolymers obtained through the separation of the polycarbonate-polyorganosiloxane copolymer by gel permeation chromatography.