JP2010043201A5 - - Google Patents

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JP2010043201A5
JP2010043201A5 JP2008208745A JP2008208745A JP2010043201A5 JP 2010043201 A5 JP2010043201 A5 JP 2010043201A5 JP 2008208745 A JP2008208745 A JP 2008208745A JP 2008208745 A JP2008208745 A JP 2008208745A JP 2010043201 A5 JP2010043201 A5 JP 2010043201A5
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stirring
methylene chloride
reaction vessel
demineralized water
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JP2008208745A
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JP2010043201A (en
JP5315851B2 (en
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実施例4−2・ポリカーボネート(5)の重合
反応槽に、撹拌しながら、先に調製したビスフェノールA/Cオリゴマー溶液(745.79g)、塩化メチレン(771.60g)、p−tert−ブチルフェノール(0.3237g)を加え、内部温度を10℃にした。
別途、25重量%水酸化ナトリウム水溶液(86.97g)、脱塩水(275.17g)、2重量%トリエチルアミン水溶液(2.51mL)を均一に混合したものを調製し、これを先の反応槽に仕込み、5時間撹拌を続けた。
塩化メチレン(2124.34g)、脱塩水(481.51g)を反応槽に添加し、20分間そのまま撹拌した後、撹拌を停止し、水層と有機層を分離した。
以降、実施例1−2と同様の洗浄、分液、溶媒除去および乾燥操作を行って、目的のポリカーボネート(5)を得た。分析値を表2に示す。構造式を以下に示す。

Figure 2010043201
Example 4-2 Polymerization of Polycarbonate (5) While stirring, the previously prepared bisphenol A / C oligomer solution (745.79 g), methylene chloride (771.60 g), p-tert-butylphenol ( 0.3237 g) was added to bring the internal temperature to 10 ° C.
Separately, a 25% by weight sodium hydroxide aqueous solution (86.97 g), demineralized water (275.17 g), and 2% by weight triethylamine aqueous solution (2.51 mL) were uniformly mixed, and this was added to the previous reaction vessel. The charging was continued for 5 hours.
Methylene chloride (2124.34 g) and demineralized water (481.51 g) were added to the reaction vessel, and the mixture was stirred as it was for 20 minutes. Then, the stirring was stopped and the aqueous layer and the organic layer were separated.
Later, a similar washing, liquid separation as in Example 1-2, and subjected to solvent removal and drying operation, to obtain a port Rica Boneto object (5). The analytical values are shown in Table 2. The structural formula is shown below.
Figure 2010043201

JP2008208745A 2008-08-13 2008-08-13 Polycarbonate resin, coating solution for electrophotographic photoreceptor using the same, and electrophotographic photoreceptor Active JP5315851B2 (en)

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JP2008208745A JP5315851B2 (en) 2008-08-13 2008-08-13 Polycarbonate resin, coating solution for electrophotographic photoreceptor using the same, and electrophotographic photoreceptor

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JP2008208745A JP5315851B2 (en) 2008-08-13 2008-08-13 Polycarbonate resin, coating solution for electrophotographic photoreceptor using the same, and electrophotographic photoreceptor

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JP2010043201A JP2010043201A (en) 2010-02-25
JP2010043201A5 true JP2010043201A5 (en) 2011-09-22
JP5315851B2 JP5315851B2 (en) 2013-10-16

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EP2557105B1 (en) * 2010-03-31 2014-12-10 Mitsubishi Chemical Corporation Polycarbonate resin, composition of said resin, and molded body of said resin
JP2011219636A (en) * 2010-04-09 2011-11-04 Mitsubishi Chemicals Corp Method for producing polycarbonate resin, and polycarbonate resin
JP5922879B2 (en) * 2010-05-14 2016-05-24 三菱化学株式会社 Polycarbonate resin composition and polycarbonate resin molded body
JP5953691B2 (en) * 2011-09-29 2016-07-20 三菱化学株式会社 Method for producing polycarbonate resin
WO2015005442A1 (en) 2013-07-12 2015-01-15 三菱化学株式会社 Electrophotographic photoreceptor, electrophotographic photoreceptor cartridge, image formation device, and polyarylate resin
JP6354506B2 (en) * 2013-10-01 2018-07-11 三菱ケミカル株式会社 Electrophotographic photosensitive member, electrophotographic photosensitive member cartridge, and image forming apparatus

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JP3778756B2 (en) * 1999-02-10 2006-05-24 帝人化成株式会社 Halogenated carbonate compound, method for producing the same, and flame-retardant resin composition using the same
JP4800468B2 (en) * 2000-09-06 2011-10-26 出光興産株式会社 Electrophotographic photoreceptor
JP2003206349A (en) * 2002-01-10 2003-07-22 Mitsubishi Chemicals Corp Polycarbonate copolymer, its manufacturing method, and electrophotographic photoreceptor using it
JP4067417B2 (en) * 2003-02-07 2008-03-26 三菱化学株式会社 Electrophotographic photoreceptor
JP4155061B2 (en) * 2003-03-03 2008-09-24 三菱化学株式会社 Method for producing polycarbonate copolymer for electrophotographic photoreceptor and electrophotographic photoreceptor

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