NO333581B1 - Vannfortynnbare foretrede melaminformaldehydharpikser, fremgangsmate for deres fremstilling samt anvendelse derav - Google Patents
Vannfortynnbare foretrede melaminformaldehydharpikser, fremgangsmate for deres fremstilling samt anvendelse derav Download PDFInfo
- Publication number
- NO333581B1 NO333581B1 NO20022755A NO20022755A NO333581B1 NO 333581 B1 NO333581 B1 NO 333581B1 NO 20022755 A NO20022755 A NO 20022755A NO 20022755 A NO20022755 A NO 20022755A NO 333581 B1 NO333581 B1 NO 333581B1
- Authority
- NO
- Norway
- Prior art keywords
- melamine
- water
- formaldehyde
- formaldehyde resins
- dilutable
- Prior art date
Links
- 229920000877 Melamine resin Polymers 0.000 title claims abstract description 76
- 238000000034 method Methods 0.000 title claims abstract description 11
- 238000002360 preparation method Methods 0.000 title abstract description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 86
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000011541 reaction mixture Substances 0.000 claims abstract description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 23
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 claims abstract description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 8
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims description 51
- 239000011347 resin Substances 0.000 claims description 51
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 42
- 239000000243 solution Substances 0.000 claims description 34
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 21
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 19
- 238000006266 etherification reaction Methods 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 13
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 10
- 239000011521 glass Substances 0.000 claims description 10
- 239000000123 paper Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 7
- -1 aliphatic alcohols Chemical class 0.000 claims description 6
- 239000004753 textile Substances 0.000 claims description 6
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- BDPPZSFVSOBOIX-UHFFFAOYSA-N 6-nonyl-1,3,5-triazine-2,4-diamine Chemical compound CCCCCCCCCC1=NC(N)=NC(N)=N1 BDPPZSFVSOBOIX-UHFFFAOYSA-N 0.000 claims description 3
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 claims description 3
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000011111 cardboard Substances 0.000 claims description 3
- 239000003365 glass fiber Substances 0.000 claims description 3
- 229920005615 natural polymer Polymers 0.000 claims description 3
- 229920001059 synthetic polymer Polymers 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- VPVSTMAPERLKKM-UHFFFAOYSA-N glycoluril Chemical compound N1C(=O)NC2NC(=O)NC21 VPVSTMAPERLKKM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 235000010755 mineral Nutrition 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000011087 paperboard Substances 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- ZMGMDXCADSRNCX-UHFFFAOYSA-N 5,6-dihydroxy-1,3-diazepan-2-one Chemical class OC1CNC(=O)NCC1O ZMGMDXCADSRNCX-UHFFFAOYSA-N 0.000 claims 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 36
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 239000008367 deionised water Substances 0.000 description 15
- 229910021641 deionized water Inorganic materials 0.000 description 15
- 235000002639 sodium chloride Nutrition 0.000 description 14
- 235000011121 sodium hydroxide Nutrition 0.000 description 10
- 238000003860 storage Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 239000004640 Melamine resin Substances 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- 235000010262 sodium metabisulphite Nutrition 0.000 description 6
- QDWYPRSFEZRKDK-UHFFFAOYSA-M sodium;sulfamate Chemical compound [Na+].NS([O-])(=O)=O QDWYPRSFEZRKDK-UHFFFAOYSA-M 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 5
- 239000008098 formaldehyde solution Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 229920003180 amino resin Polymers 0.000 description 4
- 235000013877 carbamide Nutrition 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZHTJVFJXNTXXOV-UHFFFAOYSA-N 1-(5-acetyl-2,6-dimethyl-1,2-dihydropyridin-3-yl)ethanone Chemical compound CC1NC(C)=C(C(C)=O)C=C1C(C)=O ZHTJVFJXNTXXOV-UHFFFAOYSA-N 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229960004592 isopropanol Drugs 0.000 description 2
- 230000011987 methylation Effects 0.000 description 2
- 238000007069 methylation reaction Methods 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- 239000004289 sodium hydrogen sulphite Substances 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- LDTLADDKFLAYJA-UHFFFAOYSA-L sodium metabisulphite Chemical compound [Na+].[Na+].[O-]S(=O)OS([O-])=O LDTLADDKFLAYJA-UHFFFAOYSA-L 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 description 2
- XTLSNOYUBAFCBR-UHFFFAOYSA-N 1,3-diazinan-2-one;prop-1-ene;urea Chemical compound CC=C.NC(N)=O.O=C1NCCCN1 XTLSNOYUBAFCBR-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011489 building insulation material Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- QAULOJGTCHPJSY-UHFFFAOYSA-N ethene;imidazolidin-2-one;urea Chemical compound C=C.NC(N)=O.O=C1NCCN1 QAULOJGTCHPJSY-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000004296 sodium metabisulphite Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- SSGGNFYQMRDXFH-UHFFFAOYSA-N sulfanylurea Chemical compound NC(=O)NS SSGGNFYQMRDXFH-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C09D161/32—Modified amine-aldehyde condensates
-
- 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
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/40—Chemically modified polycondensates
- C08G12/42—Chemically modified polycondensates by etherifying
- C08G12/424—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
- C08G12/425—Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines
- C08G12/427—Melamine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10128420A DE10128420A1 (de) | 2001-06-12 | 2001-06-12 | Wasserverdünnbare verätherte Melamin-Formaldehyd-Harze |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20022755D0 NO20022755D0 (no) | 2002-06-10 |
NO20022755L NO20022755L (no) | 2002-12-13 |
NO333581B1 true NO333581B1 (no) | 2013-07-15 |
Family
ID=7687991
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20022755A NO333581B1 (no) | 2001-06-12 | 2002-06-10 | Vannfortynnbare foretrede melaminformaldehydharpikser, fremgangsmate for deres fremstilling samt anvendelse derav |
Country Status (11)
Country | Link |
---|---|
US (1) | US6579964B2 (pt) |
EP (1) | EP1266917B1 (pt) |
AR (1) | AR034233A1 (pt) |
AT (1) | ATE328922T1 (pt) |
BR (1) | BR0202164A (pt) |
CA (1) | CA2390324A1 (pt) |
DE (2) | DE10128420A1 (pt) |
ES (1) | ES2266349T3 (pt) |
MX (1) | MXPA02005886A (pt) |
NO (1) | NO333581B1 (pt) |
PL (1) | PL354428A1 (pt) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2382827B (en) * | 2002-01-23 | 2003-11-12 | Thermal Economics Ltd | Improved thermal insulation |
WO2004085506A1 (de) * | 2003-03-26 | 2004-10-07 | Ami Agrolinz Melamine International Gmbh | Aminotriazin-kondensationsprodukt, verwendung eines aminotriazin-kondensationsproduktes und verfahren zur herstellung des aminotriazin-kondensationsproduktes |
US20070072976A1 (en) * | 2005-09-29 | 2007-03-29 | Ineos Melamines Gmbh | Modified aminoplast resin solutions |
WO2011095376A1 (de) * | 2010-02-08 | 2011-08-11 | Construction Research & Technology Gmbh | Sulfoniertes kondensationsprodukt |
EP2758568B1 (en) | 2011-09-21 | 2020-01-15 | Donaldson Company, Inc. | Fine fibers made from polymer crosslinked with resinous aldehyde composition |
EP2758569A4 (en) | 2011-09-21 | 2015-07-08 | Donaldson Co Inc | FIBERS COMPOSED OF SOLUBLE POLYMERS |
BR122022002492B1 (pt) | 2013-03-09 | 2022-10-11 | Donaldson Company, Inc | Fibras finas feitas a partir de aditivos de reação |
WO2018115060A1 (en) | 2016-12-21 | 2018-06-28 | Basf Se | Process for preparing liquid compositions of etherified melamine formaldehyde resins |
CN110845681A (zh) * | 2019-11-28 | 2020-02-28 | 山东兄弟科技股份有限公司 | 一种改进的乙二醇改性三聚氰胺甲醛树脂的制备方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2928758A (en) | 1958-12-12 | 1960-03-15 | West Point Mfg Co | Treating process |
DE1595206A1 (de) | 1964-08-12 | 1970-04-16 | Reichhold Albert Chemie Ag | Verfahren zur Herstellung formaldehydarmer,veraetherter Aminotriazinharze |
US3487048A (en) | 1967-10-05 | 1969-12-30 | Fiberglas Canada Ltd | Production of water soluble or water dispersible methylated melamine-formaldehyde resins consisting largely of tri-methyl ether of tri-methylol melamine |
DE2259680C3 (de) | 1972-12-06 | 1975-10-16 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung wasserlöslicher, chlorechter Appreturmittel für Zellulose enthaltende oder daraus bestehende Textilien |
DE2502168C3 (de) * | 1975-01-21 | 1979-05-17 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung wäßriger Lösungen von Melamin-Formaldehyd-Kondensaten und deren Verwendung |
DE2637424A1 (de) * | 1976-08-20 | 1978-02-23 | Basf Ag | Verfahren zur herstellung hochreaktiver traenkharze |
JPS5624415A (en) | 1979-08-04 | 1981-03-09 | Hitachi Chem Co Ltd | Production of amino resin containing less unreacted formaldehyde |
FR2559491A1 (fr) * | 1984-02-09 | 1985-08-16 | Protex Manuf Prod Chimiq | Procede de reduction de la teneur en formol libre des resines destinees au finissage sur textiles ainsi que les textiles ayant subi ces traitements |
DE3430248A1 (de) | 1984-08-17 | 1986-02-27 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von lagerstabilen, waessrigen melamin-formaldehydharz-loesungen |
DE19510520A1 (de) | 1995-03-23 | 1996-09-26 | Hoechst Ag | Wäßrige Dispersionen von Aminoplastharzen, Verfahren zu ihrer Herstellung und ihre Verwendung als Härtungsmittel für wäßrige Kunstharze |
-
2001
- 2001-06-12 DE DE10128420A patent/DE10128420A1/de not_active Withdrawn
- 2001-10-31 US US10/016,095 patent/US6579964B2/en not_active Expired - Lifetime
-
2002
- 2002-05-20 AR ARP020101856A patent/AR034233A1/es unknown
- 2002-06-04 DE DE50207066T patent/DE50207066D1/de not_active Expired - Lifetime
- 2002-06-04 ES ES02012301T patent/ES2266349T3/es not_active Expired - Lifetime
- 2002-06-04 AT AT02012301T patent/ATE328922T1/de active
- 2002-06-04 EP EP02012301A patent/EP1266917B1/de not_active Expired - Lifetime
- 2002-06-07 BR BR0202164-1A patent/BR0202164A/pt not_active IP Right Cessation
- 2002-06-10 NO NO20022755A patent/NO333581B1/no not_active IP Right Cessation
- 2002-06-11 CA CA002390324A patent/CA2390324A1/en not_active Abandoned
- 2002-06-11 PL PL02354428A patent/PL354428A1/xx not_active Application Discontinuation
- 2002-06-12 MX MXPA02005886A patent/MXPA02005886A/es active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
NO20022755L (no) | 2002-12-13 |
CA2390324A1 (en) | 2002-12-12 |
NO20022755D0 (no) | 2002-06-10 |
MXPA02005886A (es) | 2006-01-16 |
ATE328922T1 (de) | 2006-06-15 |
EP1266917A1 (de) | 2002-12-18 |
DE10128420A1 (de) | 2002-12-19 |
EP1266917B1 (de) | 2006-06-07 |
ES2266349T3 (es) | 2007-03-01 |
US20020198355A1 (en) | 2002-12-26 |
AR034233A1 (es) | 2004-02-04 |
US6579964B2 (en) | 2003-06-17 |
BR0202164A (pt) | 2003-04-22 |
DE50207066D1 (de) | 2006-07-20 |
PL354428A1 (en) | 2002-12-16 |
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