WO1996017879A1 - Binder composition comprising amine polyol reaction product - Google Patents
Binder composition comprising amine polyol reaction product Download PDFInfo
- Publication number
- WO1996017879A1 WO1996017879A1 PCT/US1995/015882 US9515882W WO9617879A1 WO 1996017879 A1 WO1996017879 A1 WO 1996017879A1 US 9515882 W US9515882 W US 9515882W WO 9617879 A1 WO9617879 A1 WO 9617879A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- resin composition
- reaction product
- polyol
- resin
- melamine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
Definitions
- thermosetting formaldehyde-based resins which are based on formaldehyde, has been desired because of regulatory and health concerns regarding formaldehyde. Due to the high performance, strength and rigidity of these thermosetting formaldehyde-based resins in industrial applications, replacement products maintaining suitable performance have been difficult to find.
- This invention discloses a resin composition which performs in many applications like phenol-formaldehyde and melamine-formaldehyde resins, but contain no phenol or formaldehyde.
- thermosetting, film- forming compositions which offer tensile strength, rigidity and water-resistance comparable to the phenol-formaldehyde and melamine-formaldehyde resins now in use.
- French Patent Application number 94-10186 filed August 22, 1994 by Societe Francaise Hoechst discloses a novel aminoplast resin comprising the reaction product of an amine derivative such as melamine, glycolurile or their mixtures with an aldehyde of the formula R-CHO in which R represents a dialkoxy methyl group, l,3-dioxolan-2-yl possibly substituted up to 4 and/or 5 times by one or more alkyl groups (preferably up to C 4 alkyl), or a 1,3-dioxan- 2-yl group possibly substituted up to 4, 5 and/or 6 times by one or more alkyl groups (preferably up to C 4 alkyl); in mixtures possibly with glyoxal.
- R represents a dialkoxy methyl group, l,3-dioxolan-2-yl possibly substituted up to 4 and/or 5 times by one or more alkyl groups (preferably up to C 4 alkyl), or a 1,3-dioxan- 2-y
- the subject invention provides a resin composition
- a resin composition comprising the reaction product of an amine derivative chosen from the group consisting of melamine, glycolurile or their mixtures with a C, to C g dialkoxyethanal (which may also be referred to as a dialkoxyacetaldehyde or a glyoxal mo ⁇ oacetal), the reaction product is then mixed with a polyol having 2 or more hydroxyl groups.
- the amine derivative and dialkoxyethanal can also be reacted with a dialdehyde, preferably glyoxal.
- the polyol is reacted with the reaction product.
- the resin composition comprises a reaction product mixed with a polyol.
- the reaction product is the addition product of an amine derivative with dialkoxyethanal.
- the amine derivative is either melamine, glycolurile or a mixture thereof, with melamine preferred because the products provide stronger and tougher films.
- the C, - C 8 dialkoxyethanal is reacted with the amine derivative generally at a molar ratio of 1 to 6 equivalents of dialkoxyethanal to melamine and 1 to 4 equivalents for glycolurile, preferably 2 to 4 equivalents of dialkoxyethanal to the amine derivative.
- a dialdehyde preferably glyoxal
- the dialdehyde is added generally at a level of 0.05 to 3 preferably 0.5 to 1, molar equivalents of aldehyde to the amine derivative.
- the Cj to C 8 dialkoxyethanal generally has the following formula:
- R 2 O H wherein R, and R 2 are C, - C Pain alkyl or R, and R 2 are joined to form a cyclic dioxolano or a dioxano substituent.
- the C, to C 8 dialkoxyethanol can also be described as a glyoxal monacetal in which the acetal is comprised of linear substituents or is a cyclic acetal.
- R, and R 2 are a C, - C 4 alkyl group, preferably the same group and preferably a methyl group as this is the most economical derivative which is commercially available, manufactured by Societe Francaise Hoechst and sold under the trademark Highlink DM (TM).
- a polyol having 2 or more hydroxyl groups is mixed in to form the resin composition.
- Suitable polyols include dialkylene glycol, polyalkylene glycol, glycerin, alkoxylated glycerin, polyvinyl alcohol, dextrose (and dextrose oligomers and derivatives), starch, starch derivatives, polyglycidol or polysaccharrides (and derivatives).
- Preferred polyols are dipropylene glycol, tripropoxylated glycerin, polyvinyl alcohol and mixtures thereof.
- the polyol is added at a level of at least 0.05 molar equivalents of polyol to the reaction product, preferably at least 0.1 molar equivalents.
- the resin composition comprises an amount of about 1 % to 99%, with 15 - 50% preferred of polyol by weight (dry basis) of the resin composition.
- a resin is provided which upon crosslinking provides films which are strong, hard, tough and water resistant.
- the polyol is reacted with the reaction product.
- the resultant resin composition has been shown to have significantly improved properties, namely improvement in ambient tensile and hot wet tensile for a textile product using the resin composition as a binder where the polyol is reacted with the reaction product verses being mixed with the reaction product.
- the polyol is reacted with the reaction product under the following conditions: 75 to 110° C, or at reflux; at a pH of 4-7, preferably 5.5 to 6.5; and for a time period of 0.5 to 5 hours, preferably 2-3 hours.
- an acid catalyst to the resin composition is also desirable.
- Suitable catalysts are sulfuric acid, hydrochloric acid, phosphoric acid, p-toluene sulfonic acid, methane sulfonic acid, aluminum salts such as aluminum hydroxychloride and aluminum chloride, magnesium chloride, zirconium sulfate and zinc chloride and the like. These catalysts facilitate the reaction(s) which effects the crosslinking.
- the acid catalyst is generally added in an amount of 0.1 % to 15% preferably, 1 % to 10% based on the weight (dry basis) of the reaction product.
- the resin composition obtained herein contains neither phenol nor formaldehyde but has been found to maintain the strength and integrity of phenolic resins under conditions of severe usage including high temperature and water immersion.
- This resin composition is useful as a binder for cellulosic automotive oil filters, or for fiberglass in such uses as fiberglass, textiles or insulation.
- the resin composition can be added to a hydroxyl containing polymer (e.g. polyvinyl alcohol) wherein the resin composition is used to crosslink the polymer.
- Example I A reaction product of melamine with dimethoxyethanal was prepared as follows: 12.6g (0.1 mole) melamine was mixed at ambient temperature with 31.2g (0.3 mole) of dimethoxyethanal in solution with 31.2g of water and an amount of 30% soda (sodium hydroxide) for obtaining a pH around 9. This mixture was then heated under agitation, for 2 hours at 60° C while maintaining the pH around 9 with adjustment, if necessary, with as many drops of 30% soda by weight as needed. This reaction product was a clear yellow liquid of 54% active solids after dilution with 6g of water.
- Example II A reaction product of melamine, glyoxal and dimethoxyethanal was prepared as follows: 252g (2 moles) melamine was mixed at ambient temperature with 145g (1 mole) glyoxal in aqueous solution at 40% by weight, 416g (4 moles) dimethoxyethanal in solution with 277g of water and an amount of 30% soda by weight for obtaining a pH around 7. The mixture is next heated under agitation for 2 hours at 60° C while maintaining the pH at around 7 by addition if necessary of as many drops of 30% soda as needed. Approximately 1090g of an aqueous solution containing approximately 726g of an aminoplast resin according to the invention was obtained.
- Example III A resin prepared as in Example II was comprised of 1 equivalent of glyoxal, 2 equivalents of melamine and 4 equivalents of dimethoxyethanal (60% aqueous solution) reacted together. It was a clear, viscous liquid of 67% solids. A series of blends was prepared using this resin, p-toluene sulfonic acid (pTSA) in isopropanol (IPA, 1:1) as catalyst, and various amounts of either diethylene glycol (DEG) or dipropylene glycol (DPG). Samples of these mixtures weighing 2.0 grams were cured for 75 minutes at 130° C and evaluated for film properties.
- pTSA p-toluene sulfonic acid
- IPA isopropanol
- DEG diethylene glycol
- DPG dipropylene glycol
- Example IV A resin prepared as in Example I consisted of 3 molar equivalents of dimethoxyethanal (DME) reacted onto 1 molar equivalent of melamine. This product was a clear, pale yellow liquid of 55% active solids. This resin was evaluated as a replacement for melamine-formaldehyde resin as a binder on filter paper. The resin was evaluated alone and with various polyols according to the formulations of Table 2. Aluminum chloride solution was found to be a suitable catalyst for the resin, but caused precipitation of the melamine formaldehyde resin. Phosphoric acid was therefore used as catalyst for the melamine formaldehyde resin.
- DME dimethoxyethanal
- the formulations (by dry weight) of Table 2 were applied to Whatman filter paper, achieving a 19% add-on. The paper was dried and cured for 5 minutes at 177° C (350° F).
- Example V Various melamine/DME-polyol combinations were evaluated against a melamine/formaldehyde (MF) resin and a phenol/formaldehyde (PF) resin as controls.
- the MF resin is the same used in Example IV.
- the PF resin is a precondensed aqueous resin having pH of 8.4, Brookfield viscosity of 760 cps, solids (by refractive index) of 68% and 2% free formaldehyde.
- the resins were padded onto Whatman filter paper, dried and cured at 350° F (177° C) for 5 minutes. The % add-on ranged from 19.6 to 20.4.
- the phenolic resin readily dispersed in the aqueous pad bath, but coagulated upon addition of catalyst. Therefore, it was applied without catalyst.
- the paper was tested for dry Mullen burst, Mullen burst after a 5 minute boil, cross-directional tensile at ambient temperature, 220° F (104° C), 320° F (160° C), 420° F (216° C), and Gurley stiffness (MD and CD). Formulations are shown in Table 4 and results in Table 5.
- the melamine/DME resins may allow the advantage of being fully cured, yet not so brittle as to preclude folding. This could save a step in manufacturing.
- Example VI To better understand the performance characteristics of the novel resin composition, a cure profile study was done. Resin solutions were padded onto Whatman filter paper at 20% add-on and air dried. The paper was then cured at 300° F (149° C), 350° F (177° C) or 400° F (204° C) for 0.5, 1, 2, 3 or 5 minutes. The paper was tested for ambient tensile strength (cross direction), wet tensile and hot tensile (220° F/104° C). The data indicate that the resins may be applied with a light or partial cure, then fully cured at a subsequent treatment.
- Example I resin should be a suitable crosslinking agent for various formulations containing PVOH or derivatives of PVOH or similarly hydroxylated substrates. To this end, the Example I resin was utilized as a crosslinking agent for a PVOH/acrylic graft copolymer.
- the graft copolymer consisted, on a dry basis, of 25% ultra low molecular weight, fully hydrolyzed PVOH grafted with 43.5% ethyl acrylate, 0.75% butyl acrylate, 1.5% bis-phenol-A-diepoxydiacrylate and 29.25% methyl methacrylate.
- the latex was a white, opaque dispersion with a viscosity of 300 cps at 30% solids, with pH raised to 6.5 with ammonium hydroxide.
- the formulations of Table 10 were applied to non-woven polyester roofing mat and cured 3 minutes at 350° F, achieving 23-24% add-on.
- the mat was tested for ambient tensile strength and % elongation at 180° C under loads ranging from 5 kg to 18 kg. Results are shown in Table 11. Sequabond* 145 (by Sequa Chemicals Inc.), a vinyl acetate/acrylic copolymer used commercially as a polymat roofing binder was used as the control. High tensile strength and low elongation values are desirable properties.
- Example 11 The results of Table 11 show that the resin of Example I can serve as a non-formaldehyde crosslinker for PVOH graft lattices with equal or better performance than that seen in commercial lattices using N-methylol acrylamide.
- Example IX The DME/melamine resins prepared in Example VIII which incorporated the polyols during the reaction were compared to the condensed resin in which comparable amounts of the same polyols were added to (blended into) the formulation. These resins were applied to a non-reactive substrate (polyester non-woven mat) and compared for ambient tensile and hot wet tensile. The add-on was 20% and substrates were dried and cured for 5 minutes at 350° F. The results below show significant improvement in ambient tensile and hot wet tensile for the reacted product vs. the blend.
- Example X To further illustrate the utility of this invention, a dimethoxyethanal/melamine resin as described in Example I, was added at levels of 6, 9, 12, and 18% of the total binder with 3% aluminum hydroxy dichloride as catalyst, with the remainder being the PVOH graft copolymer described in Example VII.
- the binder was applied at 22-24% add-on to a non-woven polyester roofing mat substrate, and cured for 3 minutes at 350° F. The mat was tested for ambient tensile strength and % elongation at 180° C under loads ranging from 5 to 18 kg.
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA 2203099 CA2203099C (en) | 1994-12-07 | 1995-12-04 | Binder composition comprising amine polyol reaction product |
AT95943694T ATE236939T1 (en) | 1994-12-07 | 1995-12-04 | BINDER COMPOSITION CONTAINING A REACTION PRODUCT OF AMINES AND POLYOLS |
JP51775796A JP3694027B2 (en) | 1994-12-07 | 1995-12-04 | Binder composition comprising an amine polyol reaction product |
DE1995630319 DE69530319T2 (en) | 1994-12-07 | 1995-12-04 | BINDER COMPOSITION CONTAINING AN IMPLEMENTATION PRODUCT OF AMINES AND POLYOLS |
EP95943694A EP0796288B1 (en) | 1994-12-07 | 1995-12-04 | Binder composition comprising amine polyol reaction product |
AU45102/96A AU4510296A (en) | 1994-12-07 | 1995-12-04 | Binder composition comprising amine polyol reaction product |
FI972391A FI116570B (en) | 1994-12-07 | 1997-06-05 | Binder composition containing an amine polyol reaction product |
MXPA/A/1997/004208A MXPA97004208A (en) | 1994-12-07 | 1997-06-06 | Agglutinant composition comprising an am polyol reaction product |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/350,692 US5539077A (en) | 1994-12-07 | 1994-12-07 | Resin composition |
US08/350,692 | 1994-12-07 | ||
US08/420,356 | 1995-04-11 | ||
US08/420,356 US5830978A (en) | 1994-12-07 | 1995-04-11 | Resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996017879A1 true WO1996017879A1 (en) | 1996-06-13 |
Family
ID=26996738
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/015882 WO1996017879A1 (en) | 1994-12-07 | 1995-12-04 | Binder composition comprising amine polyol reaction product |
Country Status (10)
Country | Link |
---|---|
US (2) | US5830978A (en) |
EP (1) | EP0796288B1 (en) |
JP (1) | JP3694027B2 (en) |
CN (1) | CN1078894C (en) |
AT (1) | ATE236939T1 (en) |
AU (1) | AU4510296A (en) |
CA (1) | CA2203099C (en) |
DE (1) | DE69530319T2 (en) |
FI (1) | FI116570B (en) |
WO (1) | WO1996017879A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997011119A1 (en) * | 1995-09-20 | 1997-03-27 | Cytec Technology Corp. | Formaldehyde-free crosslinkers |
WO2004094497A1 (en) * | 2003-03-31 | 2004-11-04 | Cytec Technology Corp. | Crosslinking composition |
EP1652868A1 (en) | 2004-10-29 | 2006-05-03 | Clariant (France) | Aminoplast resin composition |
US7442325B2 (en) * | 2004-09-29 | 2008-10-28 | Cytec Technology Corp. | Stabilized crosslinking composition |
WO2009073836A1 (en) * | 2007-12-06 | 2009-06-11 | Cytec Technology Corp. | Process for the preparation of a crosslinker composition |
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US7323634B2 (en) * | 1998-10-14 | 2008-01-29 | Patterning Technologies Limited | Method of forming an electronic device |
US6201095B1 (en) | 1999-06-22 | 2001-03-13 | Omnova Solutions Inc. | Color improvement of DME-melamine resins |
US6861099B2 (en) * | 2002-08-26 | 2005-03-01 | Georgia-Pacific Resins, Inc. | Ammonium hydroxide scavenged binder for low TMA fiberglass insulation products |
US20060090436A1 (en) * | 2004-10-29 | 2006-05-04 | Georgia-Pacific Resins, Inc. | Filter media saturating resole resin |
US20070155944A1 (en) * | 2005-12-30 | 2007-07-05 | Shooshtari Kiarash A | Fiberglass binder comprising cured benzohydro-benzofurane |
FR2901559B1 (en) * | 2006-05-24 | 2008-08-29 | Clariant Specialty Fine Chemicals Sas | AMINOPLAST OR PHENOPLAST RESIN BASED ON AT LEAST ONE MONOACETAL OF GLYOXAL AND GLYOXYLIC ACID, AND USES THEREOF |
US20100040832A1 (en) * | 2008-08-13 | 2010-02-18 | Saint-Gobain Technical Fabrics America, Inc. | Formaldehyde free woven and non-woven fabrics having improved hot wet tensile strength and binder formulations for same |
US20100197185A1 (en) * | 2009-01-30 | 2010-08-05 | Saint-Gobain Technical Fabrics America, Inc. | Low and ultra-low formaldehyde emission binders for non-woven glass mat |
JP5901623B2 (en) * | 2010-06-25 | 2016-04-13 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | Stable formaldehyde-free microcapsules |
CN102304337B (en) * | 2011-05-27 | 2015-04-08 | 天津市鑫源森达新材料科技有限公司 | Novel environmental-friendly modified glue for impregnated paper and preparation method thereof |
CN103945929B (en) * | 2011-11-10 | 2016-03-16 | 弗门尼舍有限公司 | Stable formaldehydeless microcapsules |
US8791198B2 (en) | 2012-04-30 | 2014-07-29 | H.B. Fuller Company | Curable aqueous composition |
US9416294B2 (en) | 2012-04-30 | 2016-08-16 | H.B. Fuller Company | Curable epoxide containing formaldehyde-free compositions, articles including the same, and methods of using the same |
US11472987B2 (en) * | 2012-06-07 | 2022-10-18 | Johns Manville | Formaldehyde free binder compositions with urea-aldehyde reaction products |
US8980774B2 (en) | 2012-06-15 | 2015-03-17 | Hexion Inc. | Compositions and methods for making polyesters and articles therefrom |
EP2749595B1 (en) * | 2012-12-27 | 2018-07-11 | Dow Global Technologies LLC | A crosslinkable composition and method of producing the same |
DE102013217654B4 (en) * | 2013-09-04 | 2017-02-16 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Formaldehyde-free amino or amide resins based on a reactive protective group and a di- or trialdehyde as a network former |
CN109235129A (en) * | 2018-10-11 | 2019-01-18 | 杭州富阳青禾化工有限公司 | Water repellent agent and its preparation method and application, Paper Coating coating |
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US3420799A (en) * | 1966-06-29 | 1969-01-07 | Jefferson Chem Co Inc | Process for preparing aminoplasts from alkoxyacetaldehyde with an azine |
US4835320A (en) * | 1986-06-03 | 1989-05-30 | Societe Francaise Hoechst | Process for the preparation of glyoxal monoactals |
US4851577A (en) * | 1986-03-13 | 1989-07-25 | Societe Francaise Hoechst | New substituted derivatives of N-ethyl(meth)acrylamide and a method for the preparation thereof |
US4968774A (en) * | 1989-01-10 | 1990-11-06 | Societe Francaise Hoechst | Amino-plastic resins intended for the improvement of cellulosed fibres and their application |
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US496874A (en) * | 1893-05-09 | Chaeles p | ||
DE2163853B2 (en) * | 1971-12-22 | 1974-09-19 | Basf Ag, 6700 Ludwigshafen | Process for the production of textile finishing agents |
DE2616983C2 (en) * | 1976-04-17 | 1978-12-07 | Hoechst Ag, 6000 Frankfurt | Process for the joint fixing and condensation of pigment prints or pad dyeing and high-quality finishing products |
US4198462A (en) * | 1978-08-02 | 1980-04-15 | American Cyanamid Company | Processes for preparing textile finishing composition and finishing textile materials therewith |
US4471087A (en) * | 1983-02-28 | 1984-09-11 | Diamond Shamrock Chemicals Company | Formaldehyde-free insolubilizers for binders for paper coating compositions |
FR2613361B1 (en) * | 1987-04-02 | 1989-07-21 | Hoechst France | SUBSTITUTED UREAS, THEIR PREPARATION PROCESS AND THEIR APPLICATION IN PARTICULAR IN THE ENNOBLISSEMENT OF CELLULOSIC FIBERS |
FR2723742B1 (en) * | 1994-08-22 | 1996-11-15 | Hoechst France | AMINOPLAST RESINS AND THEIR APPLICATION AS A CELLULOSE CROSS-LINING. |
US5539077A (en) * | 1994-12-07 | 1996-07-23 | Sequa Chemicals, Inc. | Resin composition |
-
1995
- 1995-04-11 US US08/420,356 patent/US5830978A/en not_active Expired - Lifetime
- 1995-12-04 WO PCT/US1995/015882 patent/WO1996017879A1/en active IP Right Grant
- 1995-12-04 EP EP95943694A patent/EP0796288B1/en not_active Expired - Lifetime
- 1995-12-04 CA CA 2203099 patent/CA2203099C/en not_active Expired - Fee Related
- 1995-12-04 CN CN95196671A patent/CN1078894C/en not_active Expired - Lifetime
- 1995-12-04 AU AU45102/96A patent/AU4510296A/en not_active Abandoned
- 1995-12-04 DE DE1995630319 patent/DE69530319T2/en not_active Expired - Lifetime
- 1995-12-04 JP JP51775796A patent/JP3694027B2/en not_active Expired - Fee Related
- 1995-12-04 AT AT95943694T patent/ATE236939T1/en active
-
1997
- 1997-02-28 US US08/807,253 patent/US5691426A/en not_active Expired - Lifetime
- 1997-06-05 FI FI972391A patent/FI116570B/en not_active IP Right Cessation
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US3420799A (en) * | 1966-06-29 | 1969-01-07 | Jefferson Chem Co Inc | Process for preparing aminoplasts from alkoxyacetaldehyde with an azine |
US4851577A (en) * | 1986-03-13 | 1989-07-25 | Societe Francaise Hoechst | New substituted derivatives of N-ethyl(meth)acrylamide and a method for the preparation thereof |
US4835320A (en) * | 1986-06-03 | 1989-05-30 | Societe Francaise Hoechst | Process for the preparation of glyoxal monoactals |
US4968774A (en) * | 1989-01-10 | 1990-11-06 | Societe Francaise Hoechst | Amino-plastic resins intended for the improvement of cellulosed fibres and their application |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997011119A1 (en) * | 1995-09-20 | 1997-03-27 | Cytec Technology Corp. | Formaldehyde-free crosslinkers |
WO2004094497A1 (en) * | 2003-03-31 | 2004-11-04 | Cytec Technology Corp. | Crosslinking composition |
US7442325B2 (en) * | 2004-09-29 | 2008-10-28 | Cytec Technology Corp. | Stabilized crosslinking composition |
US8043526B2 (en) | 2004-09-29 | 2011-10-25 | Cytec Technology Corp. | Stabilized crosslinking composition |
EP1652868A1 (en) | 2004-10-29 | 2006-05-03 | Clariant (France) | Aminoplast resin composition |
US7169881B2 (en) | 2004-10-29 | 2007-01-30 | Clariant (France) | Aminoplast resin compositions |
US7399529B2 (en) | 2004-10-29 | 2008-07-15 | Clariant (France) | Aminoplast resin composition |
WO2009073836A1 (en) * | 2007-12-06 | 2009-06-11 | Cytec Technology Corp. | Process for the preparation of a crosslinker composition |
EP2292686A1 (en) * | 2007-12-06 | 2011-03-09 | Cytec Technology Corp. | Process for the Preparation of a Crosslinker Composition |
US8460758B2 (en) | 2007-12-06 | 2013-06-11 | Cytec Technology Corp. | Process for the preparation of a crosslinker composition |
AU2008333838B2 (en) * | 2007-12-06 | 2014-04-24 | Allnex Ip S.A.R.L. | Process for the preparation of a crosslinker composition |
RU2531809C2 (en) * | 2007-12-06 | 2014-10-27 | Аллнекс США Инк., | Method of preparing crosslinking composition |
Also Published As
Publication number | Publication date |
---|---|
FI116570B (en) | 2005-12-30 |
MX9704208A (en) | 1997-09-30 |
CA2203099A1 (en) | 1996-06-13 |
EP0796288A4 (en) | 1998-01-28 |
FI972391A0 (en) | 1997-06-05 |
CA2203099C (en) | 2005-05-17 |
US5830978A (en) | 1998-11-03 |
JPH10510309A (en) | 1998-10-06 |
US5691426A (en) | 1997-11-25 |
FI972391A (en) | 1997-06-05 |
DE69530319T2 (en) | 2004-03-04 |
DE69530319D1 (en) | 2003-05-15 |
EP0796288B1 (en) | 2003-04-09 |
CN1078894C (en) | 2002-02-06 |
CN1169153A (en) | 1997-12-31 |
JP3694027B2 (en) | 2005-09-14 |
AU4510296A (en) | 1996-06-26 |
ATE236939T1 (en) | 2003-04-15 |
EP0796288A1 (en) | 1997-09-24 |
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