SK89299A3 - Monomer-poor polyurethane prepolymer comprising, free nco groups, process for its production and its use - Google Patents
Monomer-poor polyurethane prepolymer comprising, free nco groups, process for its production and its use Download PDFInfo
- Publication number
- SK89299A3 SK89299A3 SK892-99A SK89299A SK89299A3 SK 89299 A3 SK89299 A3 SK 89299A3 SK 89299 A SK89299 A SK 89299A SK 89299 A3 SK89299 A3 SK 89299A3
- Authority
- SK
- Slovakia
- Prior art keywords
- diisocyanate
- reaction
- nco groups
- groups
- diisocyanates
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 4
- 238000000034 method Methods 0.000 title claims description 8
- 229920001730 Moisture cure polyurethane Polymers 0.000 title abstract description 7
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 51
- 150000001298 alcohols Chemical class 0.000 claims abstract description 18
- 230000009257 reactivity Effects 0.000 claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 7
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 229920003023 plastic Polymers 0.000 claims abstract description 6
- 239000004033 plastic Substances 0.000 claims abstract description 6
- 239000011888 foil Substances 0.000 claims abstract description 5
- 238000004026 adhesive bonding Methods 0.000 claims abstract 2
- 238000006243 chemical reaction Methods 0.000 claims description 43
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
- 239000000178 monomer Substances 0.000 claims description 10
- 150000005846 sugar alcohols Polymers 0.000 claims description 6
- -1 aliphatic alcohols Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 239000004848 polyfunctional curative Substances 0.000 claims description 5
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 239000000123 paper Substances 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 150000002009 diols Chemical class 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
- 150000004072 triols Chemical class 0.000 claims 1
- 238000013508 migration Methods 0.000 abstract description 4
- 230000005012 migration Effects 0.000 abstract description 4
- 150000002739 metals Chemical class 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 abstract description 2
- 239000004814 polyurethane Substances 0.000 description 11
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 10
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 229920005862 polyol Polymers 0.000 description 8
- 150000003077 polyols Chemical class 0.000 description 8
- 229920001451 polypropylene glycol Polymers 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229920005906 polyester polyol Polymers 0.000 description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 150000003628 tricarboxylic acids Chemical class 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7607—Compounds of C08G18/7614 and of C08G18/7657
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7614—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
- C08G18/7621—Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring being toluene diisocyanate including isomer mixtures
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19700014A DE19700014A1 (de) | 1997-01-02 | 1997-01-02 | Monomerenarmes PU-Prepolymer |
PCT/EP1997/007131 WO1998029466A1 (de) | 1997-01-02 | 1997-12-18 | Monomerenarmes pu-prepolymer |
Publications (1)
Publication Number | Publication Date |
---|---|
SK89299A3 true SK89299A3 (en) | 1999-12-10 |
Family
ID=7816761
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK892-99A SK89299A3 (en) | 1997-01-02 | 1997-12-18 | Monomer-poor polyurethane prepolymer comprising, free nco groups, process for its production and its use |
Country Status (21)
Country | Link |
---|---|
US (1) | US6515164B1 (da) |
EP (1) | EP0951493B1 (da) |
JP (1) | JP4536163B2 (da) |
KR (1) | KR20000062385A (da) |
AT (1) | ATE202577T1 (da) |
AU (1) | AU5857898A (da) |
BR (1) | BR9714451A (da) |
CA (1) | CA2276523A1 (da) |
DE (2) | DE19700014A1 (da) |
DK (1) | DK0951493T3 (da) |
ES (1) | ES2158616T3 (da) |
HU (1) | HUP0000484A3 (da) |
NO (1) | NO993273L (da) |
NZ (1) | NZ336543A (da) |
PL (1) | PL189023B1 (da) |
PT (1) | PT951493E (da) |
SI (1) | SI0951493T1 (da) |
SK (1) | SK89299A3 (da) |
TR (1) | TR199901462T2 (da) |
WO (1) | WO1998029466A1 (da) |
ZA (1) | ZA9711666B (da) |
Families Citing this family (72)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19931997A1 (de) * | 1998-07-20 | 2000-01-27 | Henkel Kgaa | Monomerarmes Polyurethanbindemittel mit verbesserter Gleitmittelhaftung |
ATE258943T1 (de) * | 1999-07-02 | 2004-02-15 | Henkel Kgaa | Verwendung von polyurethanzusammensetzungen mit niedrigen monomergehalt als haftklebstoff |
ATE476455T1 (de) | 1999-11-29 | 2010-08-15 | Henkel Ag & Co Kgaa | Haftungsverstärker für monomerfreie reaktive polyurethane |
DE10013187A1 (de) * | 2000-03-17 | 2001-10-11 | Basf Ag | Hochfunktionelle Polyisocyanata |
DE10157488A1 (de) * | 2000-12-15 | 2002-06-20 | Henkel Kgaa | Polyurethan-Prepolymere mit NCO-Gruppen und niedrigem Gehalt an monomeren Polyisocyanat |
US20030212236A1 (en) * | 2001-05-01 | 2003-11-13 | Luigi Pellacani | Process for producing polyurethane elastomer |
DE10229519A1 (de) * | 2001-07-10 | 2003-01-30 | Henkel Kgaa | Reaktive Polyurethane mit einem geringen Gehalt an monomeren Diisocyanaten |
DE10150722A1 (de) * | 2001-10-13 | 2003-04-30 | Henkel Kgaa | Reaktive Polyurethan-Zusammensetzungen mit niedrigem Restmonomergehalt |
RU2004122092A (ru) * | 2001-12-18 | 2006-01-20 | Хенкель Коммандитгезелльшафт Ауф Акциен (DE) | Способ получения обедненных мономером форполимеров полиуретана |
DE10163857A1 (de) * | 2001-12-22 | 2003-07-10 | Henkel Kgaa | Reaktive Polyurethane mit einem geringen Gehalt an monomeren Diisocyanaten |
EP1338635B2 (de) * | 2002-02-22 | 2020-10-14 | Jowat AG | Polyurethan-Zusammensetzungen mit geringem Anteil an Diisocyanatmonomer(en) |
DE502005004768D1 (de) * | 2004-04-01 | 2008-09-04 | Basf Se | Polyisocyanatprepolymere und deren Verwendung zum Verguss von Nierenfiltern |
DE102004018048A1 (de) * | 2004-04-08 | 2005-11-10 | Henkel Kgaa | Verfahren zur Herstellung von Polyurethan-Prepolymeren |
US20060079661A1 (en) * | 2004-10-08 | 2006-04-13 | Zhu Huide D | Low volatile isocyanate monomer containing polyurethane prepolymer and adhesive system |
US20060223967A1 (en) * | 2005-03-29 | 2006-10-05 | Conner Mark D | Novel polyurea isocyanates |
DE102005048823A1 (de) * | 2005-10-10 | 2007-04-12 | Bayer Materialscience Ag | Reaktivsysteme, deren Herstellung und Verwendung |
US20070175621A1 (en) * | 2006-01-31 | 2007-08-02 | Cooligy, Inc. | Re-workable metallic TIM for efficient heat exchange |
US8580361B2 (en) * | 2006-02-01 | 2013-11-12 | Momentive Performance Materials Inc. | Insulated glass unit with sealant composition having reduced permeability to gas |
US7541076B2 (en) * | 2006-02-01 | 2009-06-02 | Momentive Performance Materials Inc. | Insulated glass unit with sealant composition having reduced permeability to gas |
US7569653B2 (en) | 2006-02-01 | 2009-08-04 | Momentive Performance Materials Inc. | Sealant composition having reduced permeability to gas |
US20070179236A1 (en) * | 2006-02-01 | 2007-08-02 | Landon Shayne J | Sealant composition having reduced permeability to gas |
US20070178256A1 (en) * | 2006-02-01 | 2007-08-02 | Landon Shayne J | Insulated glass unit with sealant composition having reduced permeability to gas |
DE102006059464A1 (de) * | 2006-12-14 | 2008-06-19 | Henkel Kgaa | Polyurethan-Kaschierklebstoff |
EP1947126A1 (de) | 2007-01-17 | 2008-07-23 | Sika Technology AG | Haftvermittlerzusammensetzung für Polymere Substrate |
WO2009061580A1 (en) * | 2007-11-07 | 2009-05-14 | Dow Global Technologies Inc. | Polyurethane adhesive compositions having high filler levels |
EP2062927B1 (de) | 2007-11-20 | 2016-06-29 | Henkel AG & Co. KGaA | 2K-PU-Klebstoff für Tieftemperaturanwendungen |
DE102007062316A1 (de) | 2007-12-21 | 2009-06-25 | Evonik Degussa Gmbh | Reaktive Isocyanatzusammensetzungen |
US8135563B2 (en) * | 2008-09-30 | 2012-03-13 | Texas Instruments Incorporated | Apparatus and method for evaluating the performance of systems having time-varying output characteristics |
US8410213B2 (en) | 2009-01-26 | 2013-04-02 | Michael James Barker | Primerless two-part polyurethane adhesive |
DE102009010069A1 (de) * | 2009-02-21 | 2010-08-26 | Bayer Materialscience Ag | Grundierung für mineralische Baustoffe |
EP2360196A1 (en) | 2010-02-12 | 2011-08-24 | Stichting Dutch Polymer Institute | Polyurethane prepolymer and aqueous polyurethane dispersion |
US9200160B2 (en) * | 2010-03-29 | 2015-12-01 | Momentive Performance Materials Inc. | Silylated polyurethane/polyorganosiloxane blend and sealant composition and fumed silica composition containing same |
BR112012024535A2 (pt) | 2010-03-29 | 2020-07-28 | Basf Se | método de ligação de adesivo de fusão, e, película, artigo de moldagem por injeção ou extrusado. |
EP2439219A1 (de) | 2010-10-06 | 2012-04-11 | Sika Technology AG | Verringerung des Anteils an Isocyanatgruppen aufweisenden Monomeren in feuchtigkeitshärtenden Polyurethanzusammensetzungen |
EP2439220A1 (de) | 2010-10-06 | 2012-04-11 | Sika Technology AG | Verringerung des Anteils an Isocyanatgruppen aufweisenden Monomeren in feuchtigkeitshärtenden Polyurethanzusammensetzungen |
NZ612548A (en) | 2010-12-20 | 2015-06-26 | Akzo Nobel Coatings Int Bv | Mdi based linings and membranes from prepolymers with very low free monomeric isocyanates |
KR20180004838A (ko) | 2011-02-17 | 2018-01-12 | 다우 글로벌 테크놀로지스 엘엘씨 | 탄산 칼슘을 함유하는 알콕시실란 함유 폴리우레탄 접착제 조성물 |
DE102011080513A1 (de) | 2011-08-05 | 2013-02-07 | Henkel Ag & Co. Kgaa | Monomerarme Polyurethanschäume |
CA2855120A1 (en) | 2011-11-10 | 2013-05-16 | Momentive Performance Materials Inc. | Moisture curable organopolysiloxane composition |
WO2013070227A1 (en) | 2011-11-10 | 2013-05-16 | Momentive Performance Materials Inc. | Moisture curable composition of a polymer having silyl groups |
JP6297498B2 (ja) | 2011-12-15 | 2018-03-20 | モーメンティブ・パフォーマンス・マテリアルズ・インク | 湿気硬化性オルガノポリシロキサン組成物 |
CA2859356A1 (en) | 2011-12-15 | 2013-06-20 | Momentive Performance Materials, Inc. | Moisture curable organopolysiloxane compositions |
CA2861659A1 (en) | 2011-12-29 | 2013-07-04 | Momentive Performance Materials, Inc. | Moisture curable organopolysiloxane composition |
WO2014123434A1 (en) | 2013-02-06 | 2014-08-14 | "Selena Labs" Społka Z Ograniczona Odpowiedzialnoscia | One component isocyanate prepolymer mixture for production in one step process of the polyurethane product |
WO2014126599A1 (en) | 2013-02-15 | 2014-08-21 | Momentive Performance Materials Inc. | Antifouling system comprising silicone hydrogel |
CN105143296B (zh) | 2013-02-25 | 2018-06-12 | 巴斯夫欧洲公司 | 通过引入脂族异氰酸酯降低基于聚合物多元醇的热塑性聚氨酯的变色 |
TW201434882A (zh) | 2013-03-13 | 2014-09-16 | Momentive Performance Mat Inc | 可濕氣固化之有機聚矽氧烷組成物 |
WO2014183029A2 (en) | 2013-05-10 | 2014-11-13 | Momentive Performance Materials Inc. | Non-metal catalyzed room temperature moisture curable organopolysiloxane compositions |
EP3036269A4 (en) | 2013-08-23 | 2017-04-12 | Momentive Performance Materials Inc. | Moisture curable compositions |
WO2015081146A1 (en) | 2013-11-26 | 2015-06-04 | Momentive Performance Materials Inc | Moisture curable compound with metal-arene complexes |
PL235304B1 (pl) | 2014-01-14 | 2020-06-29 | Selena Labs Spolka Z Ograniczona Odpowiedzialnoscia | Jednoskładnikowa mieszanina prepolimeru izocyjanianu oraz sposób wytwarzania pianki poliuretanowej w pojemniku dozującym w jednoetapowym procesie |
JP6291889B2 (ja) * | 2014-02-17 | 2018-03-14 | 東洋インキScホールディングス株式会社 | 接着剤組成物およびそれを用いた積層体 |
US9982173B2 (en) * | 2014-03-11 | 2018-05-29 | Sika Technology Ag | Polyurethane hot-melt adhesive having a low content of diisocyanate monomers and good cross-linking speed |
FR3021659B1 (fr) * | 2014-05-28 | 2017-11-17 | Bostik Sa | Composition de polyurethane a terminaisons nco a base de 2,4-tdi non thermofusible et a faible teneur en monomere tdi, comprenant au moins un compose isocyanate de volume molaire particulier. |
FR3021658B1 (fr) * | 2014-05-28 | 2017-12-08 | Bostik Sa | Composition de polyurethane a terminaisons nco a base mdi non thermofusible et a faible teneur en monomere mdi, comprenant au moins un compose isocyanate de volume molaire particulier. |
DE102014212999A1 (de) | 2014-07-04 | 2016-01-07 | Henkel Ag & Co. Kgaa | Polyurethan-Kaschierklebstoff enthaltend Füllstoffe |
DE112016000869T5 (de) | 2015-02-23 | 2018-01-18 | King Industries, Inc. | Härtbare Beschichtungszusammensetzungen von Silan-funktionellen Polymeren |
PL3067377T3 (pl) * | 2015-03-12 | 2023-05-02 | Henkel Ag & Co. Kgaa | Poliuretany o bardzo niskiej zawartości monomeru |
FR3045616B1 (fr) * | 2015-12-21 | 2020-07-10 | Bostik Sa | Mastics polyurethane superelastiques |
KR20180100572A (ko) | 2016-01-13 | 2018-09-11 | 헨켈 아게 운트 코. 카게아아 | 충전제를 함유하는 반응성 폴리우레탄 핫-멜트 접착제 |
MX2018011343A (es) | 2016-03-23 | 2019-01-31 | Fuller H B Co | Composicion de adhesivo termofusible reactivo. |
WO2018033551A1 (en) | 2016-08-19 | 2018-02-22 | Henkel Ag & Co. Kgaa | Method for preparing a hydrophobically modified clay |
EP3327057A1 (de) | 2016-11-25 | 2018-05-30 | Henkel AG & Co. KGaA | Polyester-freie kaschierklebstoff-zusammensetzung |
PL3327056T3 (pl) | 2016-11-25 | 2022-07-18 | Henkel Ag & Co. Kgaa | Szybko utwardzalna kompozycja kleju do laminowania o niskiej lepkości |
CN114921215A (zh) | 2016-11-25 | 2022-08-19 | 汉高股份有限及两合公司 | 不含聚酯的层合粘合剂组合物 |
EP3670576B8 (de) | 2018-12-19 | 2020-12-09 | Ems-Chemie Ag | Polyamid-formmassen für glasverbunde |
EP3683248A1 (en) * | 2019-01-17 | 2020-07-22 | Henkel AG & Co. KGaA | Process for the production of hot melt adhesives having a low emission of monomeric isocyanates |
PL3741812T3 (pl) | 2019-05-20 | 2022-10-03 | Henkel Ag & Co. Kgaa | Sposób wytwarzania co najmniej częściowo eksfoliowanej glinki z użyciem środka eksfoliującego obejmującego częściowy ester (met)akrylanu poli(tlenku alkilenu), cykliczny węglan i wodę |
WO2022171564A1 (en) | 2021-02-11 | 2022-08-18 | Basf Se | Reduction of monomeric isocyanates by porous material |
CN116897175A (zh) | 2021-02-26 | 2023-10-17 | 汉高股份有限及两合公司 | 用于结构木材粘合的阻燃粘合剂组合物 |
JP2024515436A (ja) | 2021-03-09 | 2024-04-10 | モメンティブ パフォーマンス マテリアルズ インコーポレイテッド | ケイ素系組成物およびその用途 |
WO2023229913A1 (en) | 2022-05-23 | 2023-11-30 | Momentive Performance Materials Inc. | Protective coating composition for metals and polymeric surfaces |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4038239A (en) * | 1973-11-23 | 1977-07-26 | Contech Inc. | Moisture curable polyurethane systems |
CA1074049A (en) | 1974-11-13 | 1980-03-18 | Russell Van Cleve | Polymer/polyols and polyurethane derivatives thereof |
DE2821001A1 (de) * | 1978-05-12 | 1979-11-15 | Bayer Ag | Verfahren zur herstellung von schichtstoffen |
DE3306559A1 (de) | 1983-02-25 | 1984-08-30 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von polyurethan-praepolymeren mit endstaendigen isocyanatgruppen und vermindertem restmonomergehalt |
DE3401129A1 (de) | 1984-01-14 | 1985-07-18 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung gemischter polyurethan-prepolymerer |
US4544763A (en) | 1984-10-19 | 1985-10-01 | Basf Wyandotte Corporation | Polyisocyanate binder having low toluene diisocyanate content |
US4814103A (en) * | 1988-02-18 | 1989-03-21 | Mobay Corporation | Color stable urethane prepolymer |
DE4006248A1 (de) * | 1990-02-28 | 1991-08-29 | Bayer Ag | Gemische aus urethangruppen enthaltenden praepolymeren und diisocyanatotoluolen sowie ihre verwendung |
-
1997
- 1997-01-02 DE DE19700014A patent/DE19700014A1/de not_active Withdrawn
- 1997-12-18 US US09/341,080 patent/US6515164B1/en not_active Expired - Lifetime
- 1997-12-18 PT PT97954425T patent/PT951493E/pt unknown
- 1997-12-18 KR KR1019997005952A patent/KR20000062385A/ko not_active Application Discontinuation
- 1997-12-18 NZ NZ336543A patent/NZ336543A/xx unknown
- 1997-12-18 TR TR1999/01462T patent/TR199901462T2/xx unknown
- 1997-12-18 PL PL97334288A patent/PL189023B1/pl unknown
- 1997-12-18 DE DE59703925T patent/DE59703925D1/de not_active Expired - Lifetime
- 1997-12-18 BR BR9714451A patent/BR9714451A/pt not_active IP Right Cessation
- 1997-12-18 CA CA002276523A patent/CA2276523A1/en not_active Abandoned
- 1997-12-18 JP JP52958398A patent/JP4536163B2/ja not_active Expired - Fee Related
- 1997-12-18 WO PCT/EP1997/007131 patent/WO1998029466A1/de not_active Application Discontinuation
- 1997-12-18 DK DK97954425T patent/DK0951493T3/da active
- 1997-12-18 HU HU0000484A patent/HUP0000484A3/hu unknown
- 1997-12-18 EP EP97954425A patent/EP0951493B1/de not_active Expired - Lifetime
- 1997-12-18 ES ES97954425T patent/ES2158616T3/es not_active Expired - Lifetime
- 1997-12-18 SK SK892-99A patent/SK89299A3/sk unknown
- 1997-12-18 SI SI9730113T patent/SI0951493T1/xx unknown
- 1997-12-18 AU AU58578/98A patent/AU5857898A/en not_active Abandoned
- 1997-12-18 AT AT97954425T patent/ATE202577T1/de not_active IP Right Cessation
- 1997-12-29 ZA ZA9711666A patent/ZA9711666B/xx unknown
-
1999
- 1999-07-01 NO NO993273A patent/NO993273L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0951493B1 (de) | 2001-06-27 |
JP4536163B2 (ja) | 2010-09-01 |
HUP0000484A3 (en) | 2000-11-28 |
ES2158616T3 (es) | 2001-09-01 |
TR199901462T2 (xx) | 1999-08-23 |
KR20000062385A (ko) | 2000-10-25 |
NO993273D0 (no) | 1999-07-01 |
ZA9711666B (en) | 1998-07-22 |
PL334288A1 (en) | 2000-02-14 |
PT951493E (pt) | 2001-12-28 |
ATE202577T1 (de) | 2001-07-15 |
NO993273L (no) | 1999-07-01 |
WO1998029466A1 (de) | 1998-07-09 |
US6515164B1 (en) | 2003-02-04 |
NZ336543A (en) | 2000-05-26 |
DE19700014A1 (de) | 1998-07-09 |
JP2001508097A (ja) | 2001-06-19 |
CA2276523A1 (en) | 1998-07-09 |
HUP0000484A2 (en) | 2000-07-28 |
SI0951493T1 (en) | 2001-10-31 |
EP0951493A1 (de) | 1999-10-27 |
PL189023B1 (pl) | 2005-06-30 |
AU5857898A (en) | 1998-07-31 |
DK0951493T3 (da) | 2001-10-01 |
DE59703925D1 (de) | 2001-08-02 |
BR9714451A (pt) | 2000-03-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SK89299A3 (en) | Monomer-poor polyurethane prepolymer comprising, free nco groups, process for its production and its use | |
US4623709A (en) | Adhesives based on polyurethane prepolymers having a low residual monomer content | |
JP4986447B2 (ja) | アルコキシシラン官能性組成物 | |
EP3067377B1 (en) | Ultralow monomer polyurethanes | |
EP2493946B1 (en) | Aqueous formulations based on crystalline or semicrystalline polyurethane polymers | |
EP2547744B1 (en) | Silane moisture curable hot melts | |
US20080071057A1 (en) | Curable composition | |
US4487910A (en) | Process for polyurethane prepolymers containing terminal isocyanate groups and having a reduced residual monomer content | |
CN110520498B (zh) | 具有耐化学品性的聚氨酯粘合剂 | |
JPH06340860A (ja) | ポリウレタンを含む水性分散液を接着剤として使用する方法 | |
US7253244B2 (en) | Fast setting 1k-polyurethane glue | |
US3915935A (en) | Polyurethane adhesive comprising a polyester and a prepolymer of the same polyester | |
WO2011144532A1 (en) | Polyurethane dispersions with an acid-base mixture as an additive | |
JP2009096996A (ja) | 粘着剤用主剤およびその製造方法、ウレタン樹脂系粘着剤製造用組成物、ならびにウレタン樹脂系粘着剤の製造方法 | |
TW201540739A (zh) | 經矽烷改質之甲醯胺 | |
EP0175474A2 (en) | Polyurethane adhesive compositions | |
JP2906029B2 (ja) | 熱溶融型アクリル系感圧接着剤組成物 | |
CA2656325A1 (en) | Prepolymers | |
CZ239699A3 (cs) | Polyurethanové prepolymery | |
MXPA99006031A (en) | Monomer-poor polyurethane prepolymer | |
JP2024024542A (ja) | ウレタンプレポリマー及びその製造方法 | |
KR20240065244A (ko) | 개선된 열안정성을 갖는 수분 경화성 폴리우레탄 핫멜트 접착제 |