AU2001288269A1 - Process for continuous production of reactive polymers with in-line post-modification and products thereof - Google Patents

Process for continuous production of reactive polymers with in-line post-modification and products thereof

Info

Publication number: AU2001288269A1
Authority: AU; Australia
Prior art keywords: polymeric product; reaction zone; unsaturated; polymerization process; side chains
Prior art date: 2000-08-25
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

AU2001288269A

Other languages

English (en)

Inventor

Michihiro Kaai

Yasuhiko Mori

David D. Schatz

Warunee Srisiri-Sisson

Marco A. Villalobos

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Johnson Polymer LLC

Original Assignee

Johnson Polymer LLC

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-08-25

Filing date

2001-08-16

Publication date

2002-03-13

2001-08-16 Application filed by Johnson Polymer LLC filed Critical Johnson Polymer LLC

2002-03-13 Publication of AU2001288269A1 publication Critical patent/AU2001288269A1/en

Status Abandoned legal-status Critical Current

Links

229920013730 reactive polymer Polymers 0.000 title claims abstract description 130
238000000034 method Methods 0.000 title claims description 45
230000008569 process Effects 0.000 title claims description 32
238000012986 modification Methods 0.000 title description 25
238000010924 continuous production Methods 0.000 title description 8
238000006243 chemical reaction Methods 0.000 claims abstract description 236
239000000178 monomer Substances 0.000 claims abstract description 124
239000003607 modifier Substances 0.000 claims abstract description 60
239000000376 reactant Substances 0.000 claims abstract description 60
238000006116 polymerization reaction Methods 0.000 claims abstract description 54
125000000524 functional group Chemical group 0.000 claims abstract description 52
230000000295 complement effect Effects 0.000 claims abstract description 4
230000000379 polymerizing effect Effects 0.000 claims abstract description 4
229920000058 polyacrylate Polymers 0.000 claims description 62
229920000642 polymer Polymers 0.000 claims description 59
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 48
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 40
239000002904 solvent Substances 0.000 claims description 37
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 33
238000000576 coating method Methods 0.000 claims description 32
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 29
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-1 styrenics Substances 0.000 claims description 19
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ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims 4
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125000002009 alkene group Chemical group 0.000 claims 2
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238000004519 manufacturing process Methods 0.000 description 25
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239000002253 acid Substances 0.000 description 13
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 13
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 12
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239000003054 catalyst Substances 0.000 description 10
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
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239000004820 Pressure-sensitive adhesive Substances 0.000 description 9
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239000000194 fatty acid Substances 0.000 description 9
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150000002978 peroxides Chemical class 0.000 description 9
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 8
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
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239000004831 Hot glue Substances 0.000 description 8
238000001816 cooling Methods 0.000 description 8
235000014113 dietary fatty acids Nutrition 0.000 description 8
229930195729 fatty acid Natural products 0.000 description 8
238000012545 processing Methods 0.000 description 8
238000005886 esterification reaction Methods 0.000 description 7
230000007246 mechanism Effects 0.000 description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
150000008065 acid anhydrides Chemical class 0.000 description 6
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229920001577 copolymer Polymers 0.000 description 6
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 6
230000032050 esterification Effects 0.000 description 6
239000000126 substance Substances 0.000 description 6
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XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 5
230000005494 condensation Effects 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
239000007788 liquid Substances 0.000 description 5
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229920005862 polyol Polymers 0.000 description 5
239000000243 solution Substances 0.000 description 5
UQFSVBXCNGCBBW-UHFFFAOYSA-M tetraethylammonium iodide Chemical compound [I-].CC[N+](CC)(CC)CC UQFSVBXCNGCBBW-UHFFFAOYSA-M 0.000 description 5
239000008096 xylene Substances 0.000 description 5
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BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
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RUZYUOTYCVRMRZ-UHFFFAOYSA-N doxazosin Chemical compound C1OC2=CC=CC=C2OC1C(=O)N(CC1)CCN1C1=NC(N)=C(C=C(C(OC)=C2)OC)C2=N1 RUZYUOTYCVRMRZ-UHFFFAOYSA-N 0.000 description 4
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ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
150000002430 hydrocarbons Chemical group 0.000 description 4
229940032007 methylethyl ketone Drugs 0.000 description 4
150000003077 polyols Chemical class 0.000 description 4
239000000758 substrate Substances 0.000 description 4
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VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 3
SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 3
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Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/14—Esterification
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2810/00—Chemical modification of a polymer
- C08F2810/30—Chemical modification of a polymer leading to the formation or introduction of aliphatic or alicyclic unsaturated groups

Landscapes

Chemical & Material Sciences (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polymerisation Methods In General (AREA)
Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)

AU2001288269A 2000-08-25 2001-08-16 Process for continuous production of reactive polymers with in-line post-modification and products thereof Abandoned AU2001288269A1 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US09648848		2000-08-25
US09/648,848 US7230048B1 (en)	2000-08-25	2000-08-25	Process for continuous production of reactive polymers with in-line post-modification and products thereof
PCT/US2001/025652 WO2002018456A2 (fr)	2000-08-25	2001-08-16	Procede de production de polymeres reactifs par post-modification en ligne et produits correspondants

Publications (1)

Publication Number	Publication Date
AU2001288269A1 true AU2001288269A1 (en)	2002-03-13

Family

ID=24602473

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AU2001288269A Abandoned AU2001288269A1 (en)	2000-08-25	2001-08-16	Process for continuous production of reactive polymers with in-line post-modification and products thereof

Country Status (11)

Country	Link
US (2)	US7230048B1 (fr)
EP (1)	EP1311560B1 (fr)
JP (1)	JP4533971B2 (fr)
KR (1)	KR100787749B1 (fr)
CN (1)	CN1308356C (fr)
AT (1)	ATE307148T1 (fr)
AU (1)	AU2001288269A1 (fr)
CA (1)	CA2421095C (fr)
DE (1)	DE60114216T2 (fr)
MX (1)	MX240540B (fr)
WO (1)	WO2002018456A2 (fr)

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US7431969B2 (en) *	2005-08-05	2008-10-07	Massachusetts Institute Of Technology	Chemical vapor deposition of hydrogel films
JP5076323B2 (ja) *	2006-01-25	2012-11-21	東亞合成株式会社	環状エーテル構造含有（共）重合体の製造方法およびその用途
CN101981065B (zh) *	2008-03-31	2013-07-24	帝斯曼知识产权资产管理有限公司	含有可自动氧化组分的涂料组合物
KR20120089857A (ko)	2009-09-30	2012-08-14	바스프 에스이	알콕실화 중합체
DE102009046922A1 (de)	2009-11-20	2011-05-26	Evonik Röhm Gmbh	Substanzpolymerisation von (Meth)acrylat-Copolymeren, die im Wässrig-alkalischen löslich sind
US9434793B1 (en) *	2015-07-24	2016-09-06	Technology Investment & Development, LLC	Continuous adiabatic inverse emulsion polymerization process

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USRE31309E (en)	1979-07-18	1983-07-12	E. I. Du Pont De Nemours And Company	High solids ambient temperature curing coatings of acrylic-fatty acid drying oil resins
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JPH0644150B2 (ja)	1986-05-09	1994-06-08	関西ペイント株式会社	プリント配線フオトレジスト用電着塗料組成物
CA1321851C (fr) *	1988-01-11	1993-08-31	Kathleen Anne Hughes	Procede pour la preparation de compositions polymeriques a groupes fonctionnels
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2000
- 2000-08-25 US US09/648,848 patent/US7230048B1/en not_active Expired - Lifetime
2001
- 2001-08-16 AU AU2001288269A patent/AU2001288269A1/en not_active Abandoned
- 2001-08-16 CA CA002421095A patent/CA2421095C/fr not_active Expired - Fee Related
- 2001-08-16 JP JP2002523969A patent/JP4533971B2/ja not_active Expired - Fee Related
- 2001-08-16 WO PCT/US2001/025652 patent/WO2002018456A2/fr active IP Right Grant
- 2001-08-16 MX MXPA03001659 patent/MX240540B/es active IP Right Grant
- 2001-08-16 KR KR1020037002723A patent/KR100787749B1/ko not_active Expired - Fee Related
- 2001-08-16 DE DE60114216T patent/DE60114216T2/de not_active Expired - Lifetime
- 2001-08-16 AT AT01967990T patent/ATE307148T1/de not_active IP Right Cessation
- 2001-08-16 EP EP01967990A patent/EP1311560B1/fr not_active Expired - Lifetime
- 2001-08-16 CN CNB018161936A patent/CN1308356C/zh not_active Expired - Fee Related
2007
- 2007-01-26 US US11/627,668 patent/US20070265399A1/en not_active Abandoned

Also Published As

Publication number	Publication date
US20070265399A1 (en)	2007-11-15
WO2002018456A3 (fr)	2002-05-30
KR20030029855A (ko)	2003-04-16
JP4533971B2 (ja)	2010-09-01
CN1466597A (zh)	2004-01-07
US7230048B1 (en)	2007-06-12
MX240540B (es)	2006-09-26
JP2004507590A (ja)	2004-03-11
WO2002018456A2 (fr)	2002-03-07
DE60114216D1 (de)	2005-11-24
MXPA03001659A (es)	2003-10-15
CA2421095A1 (fr)	2002-03-07
KR100787749B1 (ko)	2007-12-24
CN1308356C (zh)	2007-04-04
CA2421095C (fr)	2008-12-09
ATE307148T1 (de)	2005-11-15
DE60114216T2 (de)	2006-07-13
EP1311560B1 (fr)	2005-10-19
EP1311560A2 (fr)	2003-05-21

Legal Events

Date	Code	Title	Description
2007-06-07	MK5	Application lapsed section 142(2)(e) - patent request and compl. specification not accepted

Publication	Publication Date	Title
KR100619649B1 (ko)	2006-09-05	자유 라디칼 중합 및 축합 반응에 의한 중합체의 제조방법, 및 그와 관련된 장치 및 제품
Saithai et al.	2013	Effects of different epoxidation methods of soybean oil on the characteristics of acrylated epoxidized soybean oil-co-poly (methyl methacrylate) copolymer
US20070265399A1 (en)	2007-11-15	Process for continuous production of reactive polymers with in-line post-modification and products thereof
JP4237935B2 (ja)	2009-03-11	マクロマーの製造方法
US3676384A (en)	1972-07-11	Copolymers of hydroxyalkyl methacrylates and an acrylate of methacrylate ester reacted with a partially epoxidized drying oil
EP0703250B1 (fr)	1999-01-07	Polymères d'esters allyliques et d'alcool allylique ou d'alcool allylique propoxylé
JP4898072B2 (ja)	2012-03-14	部分枝分かれしたポリマー
US5480954A (en)	1996-01-02	Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols
CA1337890C (fr)	1996-01-02	Liants diluables dans l'eau et reticulables par oxydation; methode de preparation et utilisation
JP4337594B2 (ja)	2009-09-30	ポリカルボン酸マクロモノマー組成物の製造方法
EP0887361B1 (fr)	2005-01-26	Résines préparées de monomères Alpha-Beta insaturées et acides gras saturés
JPH055845B2 (fr)	1993-01-25
JPS62195002A (ja)	1987-08-27	硬化性樹脂の製造方法