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 (es) |
| EP (1) | EP0951493B1 (es) |
| JP (1) | JP4536163B2 (es) |
| KR (1) | KR20000062385A (es) |
| AT (1) | ATE202577T1 (es) |
| AU (1) | AU5857898A (es) |
| BR (1) | BR9714451A (es) |
| CA (1) | CA2276523A1 (es) |
| DE (2) | DE19700014A1 (es) |
| DK (1) | DK0951493T3 (es) |
| ES (1) | ES2158616T3 (es) |
| HU (1) | HUP0000484A3 (es) |
| NO (1) | NO993273D0 (es) |
| NZ (1) | NZ336543A (es) |
| PL (1) | PL189023B1 (es) |
| PT (1) | PT951493E (es) |
| SI (1) | SI0951493T1 (es) |
| SK (1) | SK89299A3 (es) |
| TR (1) | TR199901462T2 (es) |
| WO (1) | WO1998029466A1 (es) |
| ZA (1) | ZA9711666B (es) |
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 |
| ES2215706T3 (es) * | 1999-07-02 | 2004-10-16 | Henkel Kommanditgesellschaft Auf Aktien | Empleo de composiciones de poliuretano con contenido reducido en monomero como pegamento autoadhesivo. |
| DE50015969D1 (de) * | 1999-11-29 | 2010-09-16 | 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 |
| DE10259248A1 (de) * | 2001-12-18 | 2003-07-10 | Henkel Kgaa | Verfahren zur Herstellung von Polyurethan-Prepolymeren |
| 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) |
| ATE402208T1 (de) * | 2004-04-01 | 2008-08-15 | 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 |
| US7569653B2 (en) | 2006-02-01 | 2009-08-04 | Momentive Performance Materials Inc. | 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 |
| US20070178256A1 (en) * | 2006-02-01 | 2007-08-02 | Landon Shayne J | Insulated glass unit with 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 |
| 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 |
| EP2207830B1 (en) * | 2007-11-07 | 2018-12-26 | Dow Global Technologies LLC | 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 |
| JP2013527266A (ja) | 2010-03-29 | 2013-06-27 | ビーエーエスエフ ソシエタス・ヨーロピア | 熱可塑性ポリウレタンでのホットメルト接着 |
| 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 |
| MX344974B (es) | 2010-12-20 | 2017-01-12 | Akzo Nobel Coatings Int Bv | Membranas y revestimientos a base de mdi de los prepolimeros con muy bajo contenido de isocianatos monomericos. |
| US9085716B2 (en) | 2011-02-17 | 2015-07-21 | Dow Global Technologies Llc | Alkoxysilane containing polyurethane adhesive compositions containing calcium carbonate |
| DE102011080513A1 (de) | 2011-08-05 | 2013-02-07 | Henkel Ag & Co. Kgaa | Monomerarme Polyurethanschäume |
| WO2013070227A1 (en) | 2011-11-10 | 2013-05-16 | Momentive Performance Materials Inc. | Moisture curable composition of a polymer having silyl groups |
| WO2013071078A1 (en) | 2011-11-10 | 2013-05-16 | Momentive Performance Materials, Inc. | Moisture curable organopolysiloxane composition |
| US9523002B2 (en) | 2011-12-15 | 2016-12-20 | Momentive Performance Materials Inc. | Moisture curable organopolysiloxane compositions |
| US9663657B2 (en) | 2011-12-15 | 2017-05-30 | Momentive Performance Materials Inc. | Moisture curable organopolysiloxane compositions |
| US9527959B2 (en) | 2011-12-29 | 2016-12-27 | 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 |
| CN105229091B (zh) | 2013-02-15 | 2019-03-08 | 莫门蒂夫性能材料股份有限公司 | 包含硅水凝胶的防污体系 |
| KR20150122201A (ko) | 2013-02-25 | 2015-10-30 | 바스프 에스이 | 지방족 이소시아네이트의 도입을 통한 폴리머 폴리올계 열가소성 폴리우레탄의 변색 감소 |
| 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 |
| KR20160008584A (ko) | 2013-05-10 | 2016-01-22 | 모멘티브 퍼포먼스 머티리얼즈 인크. | 비-금속 촉매형 실온 수분 경화성 오가노폴리실록산 조성물 |
| KR20160046854A (ko) | 2013-08-23 | 2016-04-29 | 모멘티브 퍼포먼스 머티리얼즈 인크. | 수분 경화성 조성물 |
| JP6735668B2 (ja) | 2013-11-26 | 2020-08-05 | 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Ｍｏｍｅｎｔｉｖｅ Ｐｅｒｆｏｒｍａｎｃｅ Ｍａｔｅｒｉａｌｓ Ｉｎｃ． | 金属−アレーン錯体を有する湿気硬化型組成物 |
| 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 |
| WO2015135833A1 (de) * | 2014-03-11 | 2015-09-17 | Sika Technology Ag | Polyurethan-heissschmelzklebstoff mit niedrigem gehalt an monomeren diisocyanaten und guter vernetzungsgeschwindigkeit |
| 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. |
| 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. |
| DE102014212999A1 (de) | 2014-07-04 | 2016-01-07 | Henkel Ag & Co. Kgaa | Polyurethan-Kaschierklebstoff enthaltend Füllstoffe |
| WO2016137881A1 (en) | 2015-02-23 | 2016-09-01 | King Industries | Curable coating compositions of silane functional polymers |
| ES2938990T3 (es) * | 2015-03-12 | 2023-04-18 | Henkel Ag & Co Kgaa | Poliuretanos ultrabajos en monómeros |
| FR3045616B1 (fr) * | 2015-12-21 | 2020-07-10 | Bostik Sa | Mastics polyurethane superelastiques |
| CA3010144A1 (en) | 2016-01-13 | 2017-07-20 | Henkel Ag & Co. Kgaa | Reactive polyurethane hot-melt adhesives containing fillers |
| WO2017165652A1 (en) | 2016-03-23 | 2017-09-28 | H.B. Fuller Company | Reactive hot melt adhesive composition |
| CN109563313B (zh) | 2016-08-19 | 2021-08-17 | 汉高股份有限及两合公司 | 制备疏水改性的粘土的方法 |
| 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 |
| EP3327057A1 (de) | 2016-11-25 | 2018-05-30 | Henkel AG & Co. KGaA | Polyester-freie kaschierklebstoff-zusammensetzung |
| ES2913527T3 (es) | 2016-11-25 | 2022-06-02 | Henkel Ag & Co Kgaa | Composición de adhesivo de laminación de endurecimiento rápido, de baja viscosidad |
| 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 |
| ES2924345T3 (es) | 2019-05-20 | 2022-10-06 | Henkel Ag & Co Kgaa | Método para preparar una arcilla exfoliada por lo menos parcialmente utilizando un agente exfoliante que comprende un éster parcial de (meta)acrilato de poli(óxido de alquileno), un carbonato cíclico y agua |
| EP4291588A1 (en) | 2021-02-11 | 2023-12-20 | Basf Se | Reduction of monomeric isocyanates by porous material |
| AU2022226294A1 (en) | 2021-02-26 | 2023-10-12 | Henkel Ag & Co. Kgaa | Flame-retardant adhesive composition for structural wood bonding |
| WO2022192316A1 (en) | 2021-03-09 | 2022-09-15 | Momentive Performance Materials Inc. | Silicon-based compositions and applications thereof |
| 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 WO PCT/EP1997/007131 patent/WO1998029466A1/de not_active Application Discontinuation
- 1997-12-18 BR BR9714451A patent/BR9714451A/pt not_active IP Right Cessation
- 1997-12-18 DE DE59703925T patent/DE59703925D1/de not_active Expired - Lifetime
- 1997-12-18 KR KR1019997005952A patent/KR20000062385A/ko not_active Application Discontinuation
- 1997-12-18 PL PL97334288A patent/PL189023B1/pl unknown
- 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 SI SI9730113T patent/SI0951493T1/xx unknown
- 1997-12-18 TR TR1999/01462T patent/TR199901462T2/xx unknown
- 1997-12-18 AT AT97954425T patent/ATE202577T1/de not_active IP Right Cessation
- 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 NZ NZ336543A patent/NZ336543A/xx unknown
- 1997-12-18 DK DK97954425T patent/DK0951493T3/da active
- 1997-12-18 AU AU58578/98A patent/AU5857898A/en not_active Abandoned
- 1997-12-18 PT PT97954425T patent/PT951493E/pt unknown
- 1997-12-18 HU HU0000484A patent/HUP0000484A3/hu unknown
- 1997-12-18 US US09/341,080 patent/US6515164B1/en not_active Expired - Lifetime
- 1997-12-18 SK SK892-99A patent/SK89299A3/sk unknown
- 1997-12-29 ZA ZA9711666A patent/ZA9711666B/xx unknown
-
1999
- 1999-07-01 NO NO993273A patent/NO993273D0/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| SI0951493T1 (en) | 2001-10-31 |
| US6515164B1 (en) | 2003-02-04 |
| PL334288A1 (en) | 2000-02-14 |
| EP0951493B1 (de) | 2001-06-27 |
| CA2276523A1 (en) | 1998-07-09 |
| HUP0000484A3 (en) | 2000-11-28 |
| HUP0000484A2 (en) | 2000-07-28 |
| EP0951493A1 (de) | 1999-10-27 |
| DE19700014A1 (de) | 1998-07-09 |
| DK0951493T3 (da) | 2001-10-01 |
| NZ336543A (en) | 2000-05-26 |
| BR9714451A (pt) | 2000-03-21 |
| ATE202577T1 (de) | 2001-07-15 |
| ES2158616T3 (es) | 2001-09-01 |
| NO993273L (no) | 1999-07-01 |
| ZA9711666B (en) | 1998-07-22 |
| PL189023B1 (pl) | 2005-06-30 |
| TR199901462T2 (xx) | 1999-08-23 |
| KR20000062385A (ko) | 2000-10-25 |
| DE59703925D1 (de) | 2001-08-02 |
| PT951493E (pt) | 2001-12-28 |
| WO1998029466A1 (de) | 1998-07-09 |
| NO993273D0 (no) | 1999-07-01 |
| JP4536163B2 (ja) | 2010-09-01 |
| JP2001508097A (ja) | 2001-06-19 |
| AU5857898A (en) | 1998-07-31 |
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 | |
| US7253244B2 (en) | Fast setting 1k-polyurethane glue | |
| CN110520498B (zh) | 具有耐化学品性的聚氨酯粘合剂 | |
| 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 | |
| US7923574B2 (en) | Prepolymers | |
| CZ239699A3 (cs) | Polyurethanové prepolymery | |
| MXPA99006031A (es) | Prepolimero pu con bajo contenido de monomero | |
| 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 |