WO2003070783A1 - Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers - Google Patents

Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers Download PDF

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Publication number
WO2003070783A1
WO2003070783A1 PCT/US2003/004098 US0304098W WO03070783A1 WO 2003070783 A1 WO2003070783 A1 WO 2003070783A1 US 0304098 W US0304098 W US 0304098W WO 03070783 A1 WO03070783 A1 WO 03070783A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
film
monomer
forming composition
composite coating
Prior art date
Application number
PCT/US2003/004098
Other languages
English (en)
French (fr)
Inventor
Roxalana L. Martin
Edward R. Coleridge
Mark A. Tucker
Mary E. Grolemund
Original Assignee
Ppg Industries Ohio, Inc.
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.)
Filing date
Publication date
Priority claimed from US10/076,984 external-priority patent/US6686432B2/en
Application filed by Ppg Industries Ohio, Inc. filed Critical Ppg Industries Ohio, Inc.
Priority to CA 2476433 priority Critical patent/CA2476433C/en
Priority to KR1020047012561A priority patent/KR100586127B1/ko
Priority to DE2003615133 priority patent/DE60315133T2/de
Priority to BR0307662A priority patent/BR0307662A/pt
Priority to AU2003219738A priority patent/AU2003219738B2/en
Priority to JP2003569690A priority patent/JP2005517776A/ja
Priority to EP20030716009 priority patent/EP1474453B1/en
Publication of WO2003070783A1 publication Critical patent/WO2003070783A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D201/00Coating compositions based on unspecified macromolecular compounds
    • C09D201/02Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers

Definitions

  • Such copolymers may not be made using Lewis acids and/or transition metals as catalysts, and are preferably substantially free of Lewis acids and/or transition metals, in order to overcome any drawbacks associated with the use of Lewis acids and/or transition metals in coating compositions.
  • suitable aromatic diisocyanates are 4,4'-diphenylmethane diisocyanate, and toluene diisocyanate.
  • suitable aliphatic diisocyanates are straight chain aliphatic diisocyanates, such as 1 ,6- hexamethylene diisocyanate.
  • cycloaliphatic diisocyanates can be employed. Examples include isophorone diisocyanate and 4,4'-methylene- bis-(cyclohexyl isocyanate).
  • suitable higher polyisocyanates are 1,2,4-benzene triisocyanate and polymethylene polyphenyl isocyanate.
  • the polyurethanes can be prepared with unreacted carboxylic acid groups which, upon neutralization with bases such as amines, allows for dispersion into aqueous medium.
  • Stress is described as force per unit area. Although the precise mechanism by which the MICROFLUIDIZER ® emulsifier stresses the pre-emulsification mixture to particulate is not thoroughly understood, it is theorized that stress is exerted in more than one manner. It is believed that one manner in which stress is exerted is by shear; that is, the force is such that one layer or plane moves parallel to an adjacent, parallel plane. Stress can also be exerted from all sides as a bulk, compression stress. In this instance, stress could be exerted without any shear. A further manner of producing intense stress is by cavitation. Cavitation occurs when the pressure within a liquid is reduced enough to cause vaporization.
  • the polydispersity index of the copolymer is usually less than 4, in many cases less than 3.5, typically less than 3.0, and, in some cases, less than 2.5.
  • polydispersity index is determined from the following equation: (weight average molecular weight (Mw) / number average molecular weight (Mn)).
  • Mw weight average molecular weight
  • Mn number average molecular weight
  • Mn and Mw are determined from gel permeation chromatography using polystyrene standards.
  • R 6 , R 7 , and R 9 are independently selected from the group consisting of H, CF 3 , straight or branched alkyl of 1 to 20 carbon atoms, aryl, unsaturated straight or branched alkenyl or alkynyl of 2 to 10 carbon atoms, unsaturated straight or branched alkenyl of 2 to 6 carbon atoms substituted with a halogen, C 3 -C ⁇ cycloalkyl, heterocyclyl and phenyl;
  • R 8 is selected from the group consisting of H, Ci to C ⁇ alkyl, and COOR 15 , wherein R 15 is selected from the group consisting of H, an alkali metal, a Ci to C ⁇ alkyl group, glycidyl, and aryl.
  • Dynol® 604 ethoxylated acetylenic diol available from Air Products and Chemicals, Inc.
  • Cymel® 327 Highly methylated, high imino content melamine formaldehyde resin in isobutanol available from available from Cytec Industries, Inc.
PCT/US2003/004098 2002-02-15 2003-02-12 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers WO2003070783A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA 2476433 CA2476433C (en) 2002-02-15 2003-02-12 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers
KR1020047012561A KR100586127B1 (ko) 2002-02-15 2003-02-12 아이소뷰틸렌 유형 단량체의 교대 공중합체를 함유하는수성 필름-형성 조성물
DE2003615133 DE60315133T2 (de) 2002-02-15 2003-02-12 Wässrige, filmbildende zusammensetzungen enthaltend alternierende copolymere des isobutylens
BR0307662A BR0307662A (pt) 2002-02-15 2003-02-12 Composição formadora de filme e composição para revestimento compósita de vários componentes
AU2003219738A AU2003219738B2 (en) 2002-02-15 2003-02-12 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers
JP2003569690A JP2005517776A (ja) 2002-02-15 2003-02-12 イソブチレン型モノマーの交互コポリマーを含有する水系フィルム形成組成物
EP20030716009 EP1474453B1 (en) 2002-02-15 2003-02-12 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US10/076,984 US6686432B2 (en) 2002-02-15 2002-02-15 Alternating copolymers of isobutylene type monomers
US10/076,984 2002-02-15
US10/357,797 US6787597B1 (en) 2002-02-15 2003-02-04 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers
US10/357,797 2003-02-04

Publications (1)

Publication Number Publication Date
WO2003070783A1 true WO2003070783A1 (en) 2003-08-28

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2003/004098 WO2003070783A1 (en) 2002-02-15 2003-02-12 Waterborne film-forming compositions containing alternating copolymers of isobutylene type monomers

Country Status (10)

Country Link
US (1) US7101930B2 (US07101930-20060905-C00001.png)
EP (1) EP1474453B1 (US07101930-20060905-C00001.png)
JP (2) JP2005517776A (US07101930-20060905-C00001.png)
CN (1) CN1308358C (US07101930-20060905-C00001.png)
AU (1) AU2003219738B2 (US07101930-20060905-C00001.png)
BR (1) BR0307662A (US07101930-20060905-C00001.png)
CA (1) CA2476433C (US07101930-20060905-C00001.png)
DE (1) DE60315133T2 (US07101930-20060905-C00001.png)
ES (1) ES2290444T3 (US07101930-20060905-C00001.png)
WO (1) WO2003070783A1 (US07101930-20060905-C00001.png)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005016979A1 (en) * 2003-08-06 2005-02-24 Ppg Industries Ohio, Inc. Etherified carbamate functional copolymers of isobutylene type monomers, and their use in curable compositions
WO2005054305A2 (en) * 2003-11-26 2005-06-16 Ppg Industries Ohio, Inc. Method of making copolymers containing olefinic type monomers
WO2007057365A2 (de) * 2005-11-18 2007-05-24 Basf Se Verfahren zur herstellung einer wässrigen polymerisatdispersion
WO2011002831A1 (en) 2009-06-30 2011-01-06 Lubrizol Advanced Materials, Inc. Composite polymer emulsion
WO2021016613A1 (en) * 2019-07-25 2021-01-28 Ppg Industries Ohio, Inc. Acrylic polymers, aqueous polymeric dispersions prepared therefrom, and curable film-forming compositions prepared therefrom

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US6686432B2 (en) * 2002-02-15 2004-02-03 Ppg Industries Ohio, Inc. Alternating copolymers of isobutylene type monomers
TW200508286A (en) * 2003-03-25 2005-03-01 Nippon Paint Co Ltd Method of producing oil-in-water type emulsoid containing internally crosslinked fine resin particle, oil-in-water type emulsoid containing internally crosslinked fine resin particle, cation electrodeposition coating composition and substance coated
US20070014819A1 (en) * 2005-07-13 2007-01-18 Weckteck Biotechnology Company Limited Method of emulsifying phytosterol by natural saponin,emulsion prepared thereby and water dispersible phytosterol powder product
US20080163793A1 (en) * 2006-10-13 2008-07-10 Taminco Method of inhibiting nitrosamine formation in waterborne coating
US20090023862A1 (en) * 2007-07-17 2009-01-22 Ppg Industries Ohio, Inc. Solventborne thermosetting compositions containing copolymers of isobutylene type monomers
US20100160561A1 (en) * 2008-12-24 2010-06-24 Ppg Industries Ohio, Inc. Copolymers of alpha-olefin type monomers and curable film-forming compositions containing them
KR20140084267A (ko) * 2011-10-25 2014-07-04 유니-픽셀 디스플레이스, 인코포레이티드 디스플레이 장치를 위한 가요적인 내스크랫치성 필름
JP6166526B2 (ja) * 2011-12-09 2017-07-19 株式会社日本触媒 硬化性樹脂組成物及びその用途
JP6103107B2 (ja) * 2015-04-21 2017-03-29 ダイキン工業株式会社 水性分散体、塗膜及び塗装物品
EP3181595A1 (en) * 2015-12-17 2017-06-21 Lanxess Inc. Treatment of epoxidized unsaturated isoolefin copolymers
US9932486B1 (en) * 2016-10-05 2018-04-03 Eastman Chemical Company Coalescent and non-ionic surfactant blend
MX2021012092A (es) * 2019-04-04 2022-03-17 Arkema France Copolimeros acrilicos opticos hidrofobicos de calor elevado.
US20220177622A1 (en) * 2019-04-04 2022-06-09 Trinseo Europe Gmbh Impact resistant hydrophobic high heat optical acrylic copolymers
US11891466B2 (en) 2022-03-04 2024-02-06 Trinseo Europe Gmbh Heat resistant PMMA copolymers having high temperature and high humidity environmental stability for electronic component applications

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005016979A1 (en) * 2003-08-06 2005-02-24 Ppg Industries Ohio, Inc. Etherified carbamate functional copolymers of isobutylene type monomers, and their use in curable compositions
WO2005054305A2 (en) * 2003-11-26 2005-06-16 Ppg Industries Ohio, Inc. Method of making copolymers containing olefinic type monomers
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Also Published As

Publication number Publication date
JP2005517776A (ja) 2005-06-16
US7101930B2 (en) 2006-09-05
CN1308358C (zh) 2007-04-04
ES2290444T3 (es) 2008-02-16
AU2003219738B2 (en) 2005-07-14
DE60315133D1 (de) 2007-09-06
EP1474453A1 (en) 2004-11-10
BR0307662A (pt) 2005-01-04
AU2003219738A1 (en) 2003-09-09
CN1642996A (zh) 2005-07-20
CA2476433A1 (en) 2003-08-28
US20040249077A1 (en) 2004-12-09
EP1474453B1 (en) 2007-07-25
DE60315133T2 (de) 2008-04-10
JP2007297638A (ja) 2007-11-15
CA2476433C (en) 2010-06-22

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