JP2003064113A5 - - Google Patents

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JP2003064113A5
JP2003064113A5 JP2001252853A JP2001252853A JP2003064113A5 JP 2003064113 A5 JP2003064113 A5 JP 2003064113A5 JP 2001252853 A JP2001252853 A JP 2001252853A JP 2001252853 A JP2001252853 A JP 2001252853A JP 2003064113 A5 JP2003064113 A5 JP 2003064113A5
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alkyl group
carbon atoms
substituted
organic peroxide
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JP2001252853A
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JP4774172B2 (en
JP2003064113A (en
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【特許請求の範囲】
【請求項
双極子モーメント0.5以下で、沸点若しくは初留温度が110℃以上の溶媒10〜50%及び該溶媒に溶解した下記式(1)

Figure 2003064113
(式中、R は炭素数2から20のアルキル基、または水酸基で置換された炭素数1から20のアルキル基、アルコキシ基で置換された炭素数1から20のアルキル基、R 、R はそれぞれ、炭素数2から20のアルキル基、または水酸基で置換された炭素数2から20のアルキル基、アルコキシ基で置換された炭素数2から20のアルキル基、フェニル基、またはアルキル基で置換されたフェニル基、シクロアルキル基、またはアルキル基で置換されたシクロアルキル基を表す)
で示される有機過酸化物50%〜90%を含む有機過酸化物組成物。
【請求項
溶媒が初留温度140℃以上のイソパラフィン溶媒である請求項に記載の有機過酸化物組成物。
【請求項
下記式(1’)で示される新規有機過酸化物
Figure 2003064113
(式中、R’は、置換基として水酸基又はアルコキシ基を有する炭素数1から20のアルキル基、R、Rはそれぞれ、炭素数2から20のアルキル基、または水酸基で置換された炭素数2から20のアルキル基、アルコキシ基で置換された炭素数2から20のアルキル基、フェニル基、またはアルキル基で置換されたフェニル基、シクロアルキル基、またはアルキル基で置換されたシクロアルキル基を表す)
【請求項
請求項1に記載の有機過酸化物組成物を使用することを特徴とするアクリル樹脂の製造方法。
【請求項
式(1)におけるR1が水酸基又はアルコキシ基で置換された炭素数1から20のアルキル基である請求項に記載のアクリル樹脂の製造方法。
【請求項
式(1)におけるR2及びR3がそれぞれ、水酸基で置換された炭素数2から20のアルキル基又はアルコキシ基で置換された炭素数2から20のアルキル基である請求項またはに記載のアクリル樹脂の製造方法。
【請求項7】
請求項2に記載の有機過酸化物組成物を使用することを特徴とするアクリル樹脂の製造方法。 [Claims]
[Claim 1 ]
10-50% of a solvent having a dipole moment of 0.5 or less and a boiling point or initial boiling temperature of 110 ° C. or more, and the following formula (1) dissolved in the solvent:
Figure 2003064113
(Wherein, R 1 is an alkyl group having 2 to 20 carbon atoms, an alkyl group having 1 to 20 carbon atoms substituted with a hydroxyl group, an alkyl group having 1 to 20 carbon atoms substituted with an alkoxy group, R 2 , R 2 3 is an alkyl group having 2 to 20 carbon atoms, an alkyl group having 2 to 20 carbon atoms substituted with a hydroxyl group, an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group, a phenyl group, or an alkyl group, respectively. Represents a substituted phenyl group, a cycloalkyl group, or a cycloalkyl group substituted with an alkyl group)
An organic peroxide composition containing 50% to 90% of an organic peroxide represented by the formula:
[Claim 2 ]
The organic peroxide composition according to claim 1 , wherein the solvent is an isoparaffin solvent having an initial distillation temperature of 140 ° C or higher.
[Claim 3 ]
Novel organic peroxide represented by the following formula (1 ′)
Figure 2003064113
(Wherein, R 1 ′ is an alkyl group having 1 to 20 carbon atoms having a hydroxyl group or an alkoxy group as a substituent, and R 2 and R 3 are each substituted with an alkyl group having 2 to 20 carbon atoms or a hydroxyl group. An alkyl group having 2 to 20 carbon atoms, an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group, a phenyl group, or a phenyl group substituted with an alkyl group, a cycloalkyl group, or a cycloalkyl substituted with an alkyl group; Represents a group)
[Claim 4 ]
Method of manufacturing features and to luer acrylic resin using an organic peroxide composition according to claim 1.
[Claim 5 ]
The method for producing an acrylic resin according to claim 4 , wherein R1 in the formula (1) is an alkyl group having 1 to 20 carbon atoms and substituted with a hydroxyl group or an alkoxy group.
[ 6 ]
The acrylic according to claim 4 or 5 , wherein R2 and R3 in the formula (1) are each an alkyl group having 2 to 20 carbon atoms substituted with a hydroxyl group or an alkyl group having 2 to 20 carbon atoms substituted with an alkoxy group. Method of manufacturing resin.
7.
A method for producing an acrylic resin, comprising using the organic peroxide composition according to claim 2.

JP2001252853A 2001-08-23 2001-08-23 Acrylic resin production method Expired - Lifetime JP4774172B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001252853A JP4774172B2 (en) 2001-08-23 2001-08-23 Acrylic resin production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001252853A JP4774172B2 (en) 2001-08-23 2001-08-23 Acrylic resin production method

Publications (3)

Publication Number Publication Date
JP2003064113A JP2003064113A (en) 2003-03-05
JP2003064113A5 true JP2003064113A5 (en) 2008-10-02
JP4774172B2 JP4774172B2 (en) 2011-09-14

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JP2001252853A Expired - Lifetime JP4774172B2 (en) 2001-08-23 2001-08-23 Acrylic resin production method

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JP (1) JP4774172B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2971510B1 (en) * 2011-02-10 2013-03-22 Arkema France RADICAL POLYMERIZATION OF ETHYLENE STARCHED WITH HIGH-PRODUCTIVITY ORGANIC PEROXIDES
JP5861824B2 (en) * 2011-11-17 2016-02-16 スリーボンドファインケミカル株式会社 Thermosetting composition
WO2013146048A1 (en) * 2012-03-27 2013-10-03 日本ゼオン株式会社 Method for producing toner
FR3041645B1 (en) * 2015-09-29 2017-09-08 Arkema France RADICAL POLYMERIZATION OF ETHYLENE PRIMERED BY A COUPLE OF HIGH-PRODUCTIVITY ORGANIC PEROXIDES

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5791250A (en) * 1980-11-28 1982-06-07 Shin Etsu Chem Co Ltd Preparation of conductive silicone rubber sponge
JPS63168415A (en) * 1987-01-02 1988-07-12 ペンウオルト・コ−ポレ−シヨン Solution polymerization of acrylic acid derivative monomer using t-alkylhydroxyperoxide

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