HK13197A - Polyisocyanate compositions - Google Patents

Polyisocyanate compositions Download PDF

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Publication number
HK13197A
HK13197A HK13197A HK13197A HK13197A HK 13197 A HK13197 A HK 13197A HK 13197 A HK13197 A HK 13197A HK 13197 A HK13197 A HK 13197A HK 13197 A HK13197 A HK 13197A
Authority
HK
Hong Kong
Prior art keywords
isocyanate
imino
groups
reactive
prepolymer
Prior art date
Application number
HK13197A
Other languages
German (de)
English (en)
Inventor
Francis Cassidy Edward
Russell Gillis Herbert
Willem Leenslag Jan
Parfondry Alain
Original Assignee
Ici Americas Inc.
Imperial Chemical Industries Plc
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 GB878724348A external-priority patent/GB8724348D0/en
Priority claimed from GB888821186A external-priority patent/GB8821186D0/en
Application filed by Ici Americas Inc., Imperial Chemical Industries Plc filed Critical Ici Americas Inc.
Publication of HK13197A publication Critical patent/HK13197A/en

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/80Masked polyisocyanates
    • C08G18/8003Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
    • C08G18/8054Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/38
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5021Polyethers having heteroatoms other than oxygen having nitrogen
    • C08G18/5024Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5021Polyethers having heteroatoms other than oxygen having nitrogen
    • C08G18/5024Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
    • C08G18/503Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups being in latent form
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6681Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6685Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/7806Nitrogen containing -N-C=0 groups
    • C08G18/7818Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/7806Nitrogen containing -N-C=0 groups
    • C08G18/7818Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • C08G18/7831Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing biuret groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/7806Nitrogen containing -N-C=0 groups
    • C08G18/7818Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
    • C08G18/7837Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing allophanate groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/79Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/797Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing carbodiimide and/or uretone-imine groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2115/00Oligomerisation
    • C08G2115/02Oligomerisation to isocyanurate groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2120/00Compositions for reaction injection moulding processes

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Claims (9)

  1. Prépolymère à terminaison isocyanate et modification allophanate, pouvant être obtenu par réaction d'un polyol polymérique possédant une fonctionnalité hydroxyle moyenne nominale de 2 à 3 et un poids équivalent d'hydroxyle moyen de 1000 à 3000 avec au moins 5 équivalents, par équivalent d'hydroxyle, d'un isomère de diisocyanate de diphénylméthane ou de mélanges de tels isomères facultativement en association avec une petite proportion de polyphénylène-polyméthylène-polyisocyanates de plus haute fonctionnalité, le produit contenant des groupes allophanate en un rapport de ces groupes aux groupes uréthanne au moins égal à 1:4.
  2. Prépolymère suivant la revendication 1, dans lequel le rapport est au moins égal à 1:1.
  3. Prépolymère suivant la revendication 1, dans lequel le polyol polymérique est un polyéther-polyol.
  4. Prépolymère suivant la revendication 2, dans lequel le polyéther-polyol est un polyoxypropylène-diol ou -triol ou un polyoxyéthylène-oxypropylène-diol ou -triol.
  5. Formulation réactionnelle pour la préparation d'un élastomère moulé par injection-réaction, ladite formulation comprenant les constituants suivants qui sont placés dans des récipients distincts :
    (A) un prépolymère répondant à la définition suivant la revendication 1, et
    (B) un constituant réactif avec les isocyanates.
  6. Formulation réactionnelle suivant la revendication 5, dans laquelle le constituant réactif avec les isocyanates comprend une polyamine aromatique.
  7. Formulation réactionnelle suivant les revendications 5 et 6, comprenant :
    (A) un prépolymère répondant à la définition suivant la revendication 1, et
    (B) une composition réactive avec les isocyanates, comprenant :
    (i) un agent d'allongement de chaîne du type polyamine aromatique possédant une fonctionnalité amine primaire et/ou secondaire à liaison aromatique de 2 à 3,0, un poids moléculaire moyen de 100 à 400, au moins 50 moles % des entités constituant ladite polyamine consistant en diamines, et
    (ii) un polyéther à fonctionnalité amino, imino, énamino et/ou hydroxyle, possédant un nombre moyen de 1,1 à 5 groupes réactifs avec les isocyanates par molécule et ayant un poids moléculaire moyen de 1000 à 10 000.
  8. Formulation réactionnelle suivant la revendication 5, comprenant :
    (A) un prépolymère répondant à la définition suivant la revendication 1, et
    (B) une composition réactive avec les isocyanates, comprenant :
    (i) un agent d'allongement de chaîne comprenant :
    (a) 0 à 100 % d'une polyamine aromatique possédant une fonctionnalité amine primaire et/ou secondaire à liaison aromatique de 2 à 3,0, un poids moléculaire moyen de 100 à 400, au moins 50 moles % des entités formant ladite polyamine consistant en diamines, et
    (b) 100 à 0 % d'un composé aliphatique à fonctionnalité imino et/ou énamino ayant 1 à 3 groupes imino et/ou énamino réactifs avec les isocyanates par molécule et un poids moléculaire inférieur à 1000, et
    (ii) un polyéther à fonctionnalité imino et/ou énamino ayant un nombre moyen de 1,1 à 5 groupes imino et/ou énamino réactifs avec les isocyanates par molécule et un poids moléculaire moyen de 1000 à 10 000, lesdits groupes imino et/ou énamino constituant au moins 50 moles % des groupes réactifs avec les isocyanates dans ledit polyéther, et au moins 50 moles % desdits polyéthers à fonctionnalité imino et/ou énamino contenant 2 ou plus de 2 groupes imino et/ou énamino par molécule.
  9. Utilisation d'un prépolymère suivant les revendications 1 à 4 pour la préparation d'un élastomère moulé par injection-réaction.
HK13197A 1987-10-16 1997-02-05 Polyisocyanate compositions HK13197A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB878724348A GB8724348D0 (en) 1987-10-16 1987-10-16 Elastomers
GB888821186A GB8821186D0 (en) 1988-09-09 1988-09-09 Compositions of matter

Publications (1)

Publication Number Publication Date
HK13197A true HK13197A (en) 1997-02-14

Family

ID=26292912

Family Applications (1)

Application Number Title Priority Date Filing Date
HK13197A HK13197A (en) 1987-10-16 1997-02-05 Polyisocyanate compositions

Country Status (13)

Country Link
US (2) US4906674A (fr)
EP (2) EP0312366A3 (fr)
JP (2) JPH01245010A (fr)
KR (2) KR890006753A (fr)
AT (1) ATE109808T1 (fr)
AU (1) AU609197B2 (fr)
CA (1) CA1334235C (fr)
DE (1) DE3851032T2 (fr)
DK (2) DK574488A (fr)
ES (1) ES2056938T3 (fr)
HK (1) HK13197A (fr)
NZ (2) NZ226358A (fr)
PT (2) PT88774B (fr)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5142013A (en) * 1987-03-11 1992-08-25 Ici Americas Inc. Isocyanate reactive polymers having imino/enamine functionality
US5093383A (en) * 1987-03-11 1992-03-03 Ici Americas Inc. Polyurethane/urea foams from isocyanate prepolymers and isocyanate reactive imino/enamino functional reactants
GB8807684D0 (en) * 1988-03-31 1988-05-05 Ici Plc Internal mould release composition
GB8821183D0 (en) * 1988-09-09 1988-10-12 Ici America Inc Composition of matter
GB8908495D0 (en) * 1989-04-14 1989-06-01 Ici Plc Polyisocyanate compositions
US5227450A (en) * 1990-12-12 1993-07-13 Air Products And Chemicals, Inc. Hydroxyl-containing organotin catalysts for making polyurethane rim elastomers
US5256704A (en) * 1990-12-12 1993-10-26 Air Products And Chemicals, Inc. Polyurethane RIM elastomers obtained with hydroxyl-containing organotin catalysts
GB9125918D0 (en) * 1991-12-05 1992-02-05 Ici Plc Reaction system for preparing polyurethane/polyurea
US5319053A (en) * 1993-09-02 1994-06-07 Miles Inc. Liquid diphenylmethane diisocyanate
US5440003A (en) * 1993-09-02 1995-08-08 Miles Inc. Liquid methylene diphenyl diisocyanate
US5319054A (en) * 1993-09-02 1994-06-07 Miles Inc. Liquid methylene diphenyl diisocyanate
DE19502198A1 (de) * 1995-01-25 1996-08-01 Bayer Ag Verfahren zur Herstellung von Formkörpern
US6828405B1 (en) 1995-05-23 2004-12-07 The Sherwin-Williams Company Polyimine/polyisocyanate coating composition
US5591807A (en) * 1995-05-23 1997-01-07 The Sherwin-Williams Company Polyimine/polyisocyanate coating composition containing polymeric anhydride
US5567793A (en) * 1995-06-06 1996-10-22 Bayer Corporation Urethane-free, diphenylmethane diisocyanate prepolymers and process for their production
US5686042A (en) * 1995-06-07 1997-11-11 Bayer Corporation Rim process using liquid methylene diphenyl diisocyanate
US5648445A (en) * 1995-12-22 1997-07-15 Bayer Corporation Liquid 1,3-phenylene diisocyanate, 1,1'-biphenyl diisocyanate and 1,1'-oxy-bis-(isocyanato-benzene)
US5663272A (en) * 1995-12-22 1997-09-02 Bayer Corporation Allophanate-modified diphenylmethane diisocyanates and processes for their production and use
US5889068A (en) * 1997-07-24 1999-03-30 Bayer Corporation Water blown polyurethane soling systems
US5821275A (en) * 1997-11-10 1998-10-13 Bayer Corporation Flexible foams and flexible molded foams based on liquid isocyanate-terminated allophanate-modified MDI prepolymer blends and processes for the production of these foams
US5874485A (en) * 1997-11-10 1999-02-23 Bayer Corporation Flexible foams and flexible molded foams based on allophanate-modified diphenylmethane diisocyanates and processes for the production of these foams
US7087698B1 (en) * 1999-11-18 2006-08-08 Ppg Industries Ohio, Inc. Method of preparing an optical polymerizate
US7098290B1 (en) * 1999-11-18 2006-08-29 Ppg Industries Ohio, Inc. Method of preparing an optical polymerizate
US6482913B1 (en) 2000-02-07 2002-11-19 Bayer Aktiengesellschaft Liquid MDI adducts wtih improved freeze stability
US6271279B1 (en) 2000-07-10 2001-08-07 Bayer Corporation High resilient flexible urethane foam and flexible molded foams based on allophanate modified isocyanates
US8017720B2 (en) 2005-12-16 2011-09-13 Ppg Industries Ohio, Inc. Sulfur-containing oligomers and high index polyurethanes prepared therefrom
US6639040B1 (en) 2002-06-13 2003-10-28 Bayer Corporation Continuous process for the production of MDI allophanates
US7009032B2 (en) 2002-12-20 2006-03-07 Ppg Industries Ohio, Inc. Sulfide-containing polythiols
DE102004015985A1 (de) * 2004-04-01 2005-10-20 Bayer Materialscience Ag Verfärbungsstabile Polyetherallophanate
WO2006009443A1 (fr) 2004-07-21 2006-01-26 Stichting Voor De Technische Wetenschappen Polyacylurethanes bases sur des diisocyanates et des polyesterpolyols
US11591436B2 (en) 2004-09-01 2023-02-28 Ppg Industries Ohio, Inc. Polyurethane article and methods of making the same
US11008418B2 (en) 2004-09-01 2021-05-18 Ppg Industries Ohio, Inc. Polyurethanes, articles and coatings prepared therefrom and methods of making the same
US11248083B2 (en) 2004-09-01 2022-02-15 Ppg Industries Ohio, Inc. Aircraft windows
US20090280329A1 (en) 2004-09-01 2009-11-12 Ppg Industries Ohio, Inc. Polyurethanes, Articles and Coatings Prepared Therefrom and Methods of Making the Same
US11149107B2 (en) 2004-09-01 2021-10-19 Ppg Industries Ohio, Inc. Polyurethanes, articles and coatings prepared therefrom and methods of making the same
US9464169B2 (en) 2004-09-01 2016-10-11 Ppg Industries Ohio, Inc. Polyurethanes, articles and coatings prepared therefrom and methods of making the same
US9598527B2 (en) 2004-09-01 2017-03-21 Ppg Industries Ohio, Inc. Polyurethanes, articles and coatings prepared therefrom and methods of making the same
US20090280709A1 (en) 2004-09-01 2009-11-12 Ppg Industries Ohio, Inc. Polyurethanes, Articles and Coatings Prepared Therefrom and Methods of Making the Same
DE102005047560A1 (de) * 2005-10-04 2007-04-05 Bayer Materialscience Ag Zusammensetzung zur Herstellung von Polyharnstoffbeschichtungen
KR101029908B1 (ko) 2006-05-05 2011-04-18 피피지 인더스트리즈 오하이오 인코포레이티드 싸이오에터 작용성 올리고머성 폴리싸이올로부터 제조된 조성물 및 제품
US20090156777A1 (en) * 2007-12-17 2009-06-18 Nodelman Neil H Freeze-stable aromatic diisocyanates and processes for the preparation of these freeze-stable products
CA2761093C (fr) * 2009-05-19 2017-10-10 Basf Se Polyurees pouvant etre preparees a partir de deux polyetheramines et d'un prepolymere
US9090012B2 (en) * 2010-12-30 2015-07-28 Baker Hughes Incorporated Process for the preparation of conformable materials for downhole screens
US9568643B2 (en) 2012-12-13 2017-02-14 Ppg Industries Ohio, Inc. Polyurethane urea-containing compositions and optical articles and methods for preparing them
EP3129353B1 (fr) * 2014-04-11 2024-02-28 Covestro Deutschland AG Procédé de fabrication de diisocyanates de xylylène en phase gazeuse
WO2015164408A1 (fr) 2014-04-21 2015-10-29 Gaco Western, LLC Compositions de mousse
US10179830B2 (en) 2014-06-13 2019-01-15 Covestro Deutschland Ag Thioallophanate polyisocyanates containing silane groups
WO2015189169A1 (fr) * 2014-06-13 2015-12-17 Covestro Deutschland Ag Polyisocyanates ayant une structure de thioallophanate
KR102555281B1 (ko) * 2015-09-09 2023-07-14 코베스트로 도이칠란트 아게 스크래치-내성 2-성분 폴리우레탄 코팅
WO2025102202A1 (fr) * 2023-11-13 2025-05-22 万华化学集团股份有限公司 Composition de polyisocyanate et couche de revêtement présentant une résistance chimique améliorée

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3314922A (en) * 1961-08-21 1967-04-18 Du Pont Polymers and process of making same
BE637578A (fr) * 1962-09-19
GB1064841A (en) * 1963-02-04 1967-04-12 Ici Ltd Manufacture of polymers containing biuret and urea groups
DE1618422A1 (de) * 1967-05-12 1970-10-29 Bayer Ag Verfahren zur Herstellung von Isocyanaten
DE2002064C2 (de) * 1970-01-17 1983-09-01 Bayer Ag, 5090 Leverkusen Verfahren zur Herstellung von flammwidrigen elastischen oder halbelastischen Schaumstoffen
DE2043645A1 (de) * 1970-09-03 1972-03-16 Koelbel H Selbsthaltende Epoxidharze
GB1520846A (en) * 1976-05-21 1978-08-09 Ici Ltd Isocyanates
DE2729990A1 (de) * 1977-07-02 1979-01-18 Bayer Ag Verfahren zur herstellung von isocyanatgruppen aufweisenden allophanaten
DE2737670A1 (de) * 1977-08-20 1979-03-01 Bayer Ag Verfahren zur herstellung von schaumstofformkoerper
JPS5736115A (en) * 1980-08-12 1982-02-26 Mitsui Tekisako Chem Kk Curing agent composition for polyurethane
DE3215909A1 (de) * 1982-04-29 1983-11-03 Basf Ag, 6700 Ludwigshafen Verfahren zur herstellung von gegebenenfalls zellhaltigen formkoerpern aus polyharnstoff-elastomeren
US4465858A (en) * 1983-07-20 1984-08-14 Texaco Inc. Procedure for the partial alkoxylation of polyoxyalkyleneamines
US4595743A (en) * 1985-01-22 1986-06-17 The Dow Chemical Company High modulus polyurea elastomers prepared with amine-initiated polyols
US4686242A (en) * 1985-03-25 1987-08-11 The Dow Chemical Company Polyurea polymers prepared from urea containing prepolymers
US4689356A (en) * 1985-12-10 1987-08-25 The Dow Chemical Company Polyurethane elastomers prepared in a two-step process using mixtures of chain extenders
DE3607996A1 (de) * 1986-03-11 1987-09-17 Basf Ag Feuchtigkeitshaertende, lagerstabile einkomponenten-polyurethansysteme und deren verwendung
GB8705801D0 (en) * 1987-03-11 1987-04-15 Ici Plc Injection moulding compositions
US4786703A (en) * 1987-04-15 1988-11-22 Air Products And Chemicals, Inc. Process for the preparation of polyisocyanate prepolymers and polyurethanes having high temperature performance and low hysteresis
US4810820A (en) * 1987-08-12 1989-03-07 Mobay Corporation Process for the production of polyisocyanates containing allophanate groups

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DK574488D0 (da) 1988-10-14
NZ226357A (en) 1990-06-26
JPH01245010A (ja) 1989-09-29
JPH01252622A (ja) 1989-10-09
KR890006754A (ko) 1989-06-15
EP0312366A2 (fr) 1989-04-19
EP0312365A2 (fr) 1989-04-19
DE3851032D1 (de) 1994-09-15
AU609197B2 (en) 1991-04-26
EP0312365A3 (en) 1989-11-15
CA1334235C (fr) 1995-01-31
PT88774B (pt) 1992-12-31
KR970010750B1 (ko) 1997-06-30
ATE109808T1 (de) 1994-08-15
DK574488A (da) 1989-04-17
ES2056938T3 (es) 1994-10-16
KR890006753A (ko) 1989-06-15
US4906674A (en) 1990-03-06
NZ226358A (en) 1990-07-26
PT88773B (pt) 1992-12-31
DE3851032T2 (de) 1994-12-08
US4866103A (en) 1989-09-12
EP0312365B1 (fr) 1994-08-10
DK574388D0 (da) 1988-10-14
AU2376988A (en) 1989-04-20
EP0312366A3 (fr) 1989-07-26
DK574388A (da) 1989-04-17

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