NO20023453L - Viskoelastiske polyuretanskum - Google Patents
Viskoelastiske polyuretanskum Download PDFInfo
- Publication number
- NO20023453L NO20023453L NO20023453A NO20023453A NO20023453L NO 20023453 L NO20023453 L NO 20023453L NO 20023453 A NO20023453 A NO 20023453A NO 20023453 A NO20023453 A NO 20023453A NO 20023453 L NO20023453 L NO 20023453L
- Authority
- NO
- Norway
- Prior art keywords
- foam
- isocyanate
- foams
- weight
- reactive mixture
- Prior art date
Links
- 229920005830 Polyurethane Foam Polymers 0.000 title claims description 14
- 239000011496 polyurethane foam Substances 0.000 title claims description 14
- 239000006260 foam Substances 0.000 claims description 92
- 239000000203 mixture Substances 0.000 claims description 75
- 229920005862 polyol Polymers 0.000 claims description 27
- 150000003077 polyols Chemical class 0.000 claims description 27
- PLFFHJWXOGYWPR-HEDMGYOXSA-N (4r)-4-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]pentan-1-ol Chemical compound C([C@]1(C)[C@H]2CC[C@H]34)CCC(C)(C)[C@@H]1CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@@H]1[C@@H](CCCO)C PLFFHJWXOGYWPR-HEDMGYOXSA-N 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 21
- 239000012948 isocyanate Substances 0.000 claims description 19
- 150000002513 isocyanates Chemical class 0.000 claims description 19
- 239000003054 catalyst Substances 0.000 claims description 17
- 241001539019 Monolene Species 0.000 claims description 16
- 239000005056 polyisocyanate Substances 0.000 claims description 16
- 229920001228 polyisocyanate Polymers 0.000 claims description 16
- 229920000728 polyester Polymers 0.000 claims description 15
- CWKVFRNCODQPDB-UHFFFAOYSA-N 1-(2-aminoethylamino)propan-2-ol Chemical compound CC(O)CNCCN CWKVFRNCODQPDB-UHFFFAOYSA-N 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000004970 Chain extender Substances 0.000 claims description 10
- 239000004971 Cross linker Substances 0.000 claims description 9
- 230000002688 persistence Effects 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 5
- -1 polyoxypropylene Polymers 0.000 claims description 5
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- 125000006353 oxyethylene group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000003190 viscoelastic substance Substances 0.000 description 19
- 238000009472 formulation Methods 0.000 description 18
- 238000007906 compression Methods 0.000 description 14
- 230000006835 compression Effects 0.000 description 13
- 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 13
- 230000000052 comparative effect Effects 0.000 description 12
- 238000012545 processing Methods 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- 150000004998 toluenediamines Chemical class 0.000 description 5
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 150000002924 oxiranes Chemical class 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000021523 carboxylation Effects 0.000 description 3
- 238000006473 carboxylation reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 3
- 150000004072 triols Chemical class 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 125000005702 oxyalkylene group Chemical group 0.000 description 2
- 238000013031 physical testing Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical group CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 241000699729 Muridae Species 0.000 description 1
- WWEXBGFSEVKZNE-UHFFFAOYSA-N N=C=O.N=C=O.C1=CC=CC2=CC=CC=C21 Chemical class N=C=O.N=C=O.C1=CC=CC2=CC=CC=C21 WWEXBGFSEVKZNE-UHFFFAOYSA-N 0.000 description 1
- 241000269978 Pleuronectiformes Species 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000000386 athletic effect Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000004202 carbamide Chemical group 0.000 description 1
- 150000001718 carbodiimides Chemical group 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- MQKMBXOZOISLIV-UHFFFAOYSA-N dioctadecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCCCCCCC MQKMBXOZOISLIV-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 150000004000 hexols Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 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
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000013518 molded foam Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920005896 rigid polyol Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/495,192 US6391935B1 (en) | 2000-01-31 | 2000-01-31 | Viscoelastic polyurethane foams |
| PCT/IB2001/000209 WO2001057104A2 (fr) | 2000-01-31 | 2001-01-24 | Mousses de polyurethanne viscoelastiques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO20023453D0 NO20023453D0 (no) | 2002-07-18 |
| NO20023453L true NO20023453L (no) | 2002-09-17 |
Family
ID=23967642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20023453A NO20023453L (no) | 2000-01-31 | 2002-07-18 | Viskoelastiske polyuretanskum |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6391935B1 (fr) |
| EP (1) | EP1268596A2 (fr) |
| JP (1) | JP2003522235A (fr) |
| AU (1) | AU2001230455A1 (fr) |
| BR (1) | BR0107957A (fr) |
| CA (1) | CA2398507C (fr) |
| MX (1) | MXPA02007351A (fr) |
| NO (1) | NO20023453L (fr) |
| PL (1) | PL356303A1 (fr) |
| WO (1) | WO2001057104A2 (fr) |
Families Citing this family (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6790871B1 (en) | 2000-11-13 | 2004-09-14 | Woodbridge Foam Corporation | Isocyanate-based polymer foam and process for production thereof |
| US6872270B2 (en) * | 2001-04-19 | 2005-03-29 | Textile Rubber & Chemical Co. | Bubble pack cushioned composite, method of making and article made therefrom |
| EP1404736B1 (fr) * | 2001-04-27 | 2008-12-10 | Huntsman International Llc | Procede de production d'une mousse viscoelastique |
| KR100793523B1 (ko) | 2001-05-21 | 2008-01-14 | 헌트스만 인터내셔날, 엘엘씨 | 매우 연질의 폴리우레탄 탄성체 |
| US6491846B1 (en) * | 2001-06-21 | 2002-12-10 | Bayer Antwerpen, N.V. | Process for the in-situ production of polyol blends, the in-situ produced polyol blends, and their use in the production of viscoelastic foam |
| US7051389B2 (en) * | 2002-05-24 | 2006-05-30 | Tempur World, Llc | Comfort pillow |
| CA2433137A1 (fr) * | 2002-06-22 | 2003-12-22 | Wendell Martens | Systeme de matelas de mousse a memoire |
| WO2004020496A1 (fr) * | 2002-08-27 | 2004-03-11 | Shell Internationale Research Maatschappij B.V. | Combinaison de polyol |
| US7341776B1 (en) * | 2002-10-03 | 2008-03-11 | Milliren Charles M | Protective foam with skin |
| US6908979B2 (en) | 2002-11-18 | 2005-06-21 | Huntsman International Llc | Polyurethane elastomer gels |
| JP4667726B2 (ja) * | 2003-04-25 | 2011-04-13 | 倉敷紡績株式会社 | 抗菌性軟質ウレタンフォーム及びそれを用いた枕 |
| US20040266900A1 (en) * | 2003-06-26 | 2004-12-30 | Raymond Neff | Viscoelastic polyurethane foam |
| US7238730B2 (en) * | 2003-06-26 | 2007-07-03 | Basf Corporation | Viscoelastic polyurethane foam |
| US7208531B2 (en) * | 2003-06-26 | 2007-04-24 | Basf Corporation | Viscoelastic polyurethane foam |
| US7078443B2 (en) * | 2003-10-22 | 2006-07-18 | Intellectual Property Holdings, Llc | Viscoelastic foam layer and composition |
| ES2313128T3 (es) * | 2003-10-31 | 2009-03-01 | Dow Global Technologies Inc. | Sistema de aislamiento de sonido. |
| US7185604B2 (en) * | 2004-04-12 | 2007-03-06 | Debra Leah Holte | Orthopedic pet cushion |
| US8039078B2 (en) | 2004-08-26 | 2011-10-18 | Intellectual Property Holdings, Llc | Energy-absorbing pads |
| DE102004047406A1 (de) * | 2004-09-28 | 2006-03-30 | Basf Ag | Verfahren zur Herstellung von Polyurethan-Weichschaumstoffen |
| DE102004054394A1 (de) * | 2004-11-10 | 2006-05-11 | Basf Ag | Polyurethane mit einer Asker C-Härte von 1 bis 70 |
| US8419701B2 (en) * | 2005-01-10 | 2013-04-16 | The Procter & Gamble Company | Absorbent articles with stretch zones comprising slow recovery elastic materials |
| US20060160977A1 (en) * | 2005-01-14 | 2006-07-20 | Jung-Shun Ou | Prescription for preparation of non-yellowing polyurethane foam |
| JP2006249270A (ja) * | 2005-03-11 | 2006-09-21 | Nippon Polyurethane Ind Co Ltd | 粘弾性ポリウレタンフォームの製造方法 |
| JP5266756B2 (ja) * | 2005-04-21 | 2013-08-21 | 旭硝子株式会社 | 低反発性軟質ポリウレタンフォームおよびその製造方法 |
| US7469437B2 (en) | 2005-06-24 | 2008-12-30 | Tempur-Pedic Management, Inc. | Reticulated material body support and method |
| US7958573B2 (en) * | 2006-01-19 | 2011-06-14 | Gentex Corporation | Size adjustable safety and comfort liner for a helmet |
| US20070234629A1 (en) * | 2006-02-06 | 2007-10-11 | Brooks Joseph D | Self-securing spring bobber |
| TW200801060A (en) | 2006-02-28 | 2008-01-01 | Asahi Glass Co Ltd | Flexible polyurethane foam and process for producing the same |
| US8656537B2 (en) | 2006-04-20 | 2014-02-25 | Dan Foam Aps | Multi-component pillow and method of manufacturing and assembling same |
| US10023683B2 (en) * | 2006-06-12 | 2018-07-17 | Evonik Degussa Gmbh | Catalyst compositions for improving polyurethane foam performance |
| US20070299153A1 (en) | 2006-06-23 | 2007-12-27 | Hager Stanley L | Viscoelastic foams with slower recovery and improved tear |
| WO2008021034A2 (fr) * | 2006-08-10 | 2008-02-21 | Dow Global Technologies, Inc. | Procédé de préparation de mousse de polyuréthanne viscoélastique |
| TW200831550A (en) | 2006-10-25 | 2008-08-01 | Asahi Glass Co Ltd | Method for producing soft polyurethane foam |
| JP5303885B2 (ja) * | 2007-09-18 | 2013-10-02 | 旭硝子株式会社 | 軟質ポリウレタンフォームの製造方法および軟質ポリウレタンフォーム |
| EP2194084A1 (fr) * | 2007-09-28 | 2010-06-09 | Asahi Glass Company, Limited | Procédé de fabrication d'une mousse flexible de polyuréthane, procédé de fabrication d'un article moulé par pressage à chaud et article moulé par pressage à chaud |
| US20090306235A1 (en) * | 2008-06-05 | 2009-12-10 | Wang Jin Quan | Memory Foam Pad |
| ES2655387T3 (es) | 2008-07-18 | 2018-02-19 | Dow Global Technologies Llc | Estructuras celulares y espumas de poliuretano viscoelásticas |
| CN101412798B (zh) | 2008-11-21 | 2011-08-10 | 优洁（亚洲）有限公司 | 软质聚氨酯低回弹泡沫及其制备方法 |
| US8455679B2 (en) * | 2008-12-12 | 2013-06-04 | Basf Se | Prepolymer systems having reduced monomeric isocyanate contents |
| US8503688B2 (en) * | 2009-08-24 | 2013-08-06 | Gregory DiRusso | Device to enhance an ear bud |
| USD617503S1 (en) | 2010-01-27 | 2010-06-08 | Intellectual Property Holdings, Llc | Helmet pad structure |
| US8726424B2 (en) | 2010-06-03 | 2014-05-20 | Intellectual Property Holdings, Llc | Energy management structure |
| KR101914020B1 (ko) | 2010-09-07 | 2018-10-31 | 다우 글로벌 테크놀로지스 엘엘씨 | 낮은 영구 압축 변형률 및 높은 공기 유동의 ｍｄｉ 점탄성 폴리우레탄 발포체 제조 방법 |
| ES2745737T3 (es) | 2010-09-29 | 2020-03-03 | Dow Global Technologies Llc | Proceso para fabricar espuma de poliuretano viscoelástica con deformación por compresión baja y circulación de aire alta |
| US20140000016A1 (en) * | 2010-12-09 | 2014-01-02 | Claudio Storelli | Slow Rebound Foam Padded Sports Shirt |
| USD679058S1 (en) | 2011-07-01 | 2013-03-26 | Intellectual Property Holdings, Llc | Helmet liner |
| US9516910B2 (en) | 2011-07-01 | 2016-12-13 | Intellectual Property Holdings, Llc | Helmet impact liner system |
| US8975335B2 (en) | 2011-09-23 | 2015-03-10 | Bayer Materialscience Llc | Process for the production of high air flow polyether foams and the foams produced by this process |
| USD683079S1 (en) | 2011-10-10 | 2013-05-21 | Intellectual Property Holdings, Llc | Helmet liner |
| EP2599810A1 (fr) | 2011-12-02 | 2013-06-05 | Basf Se | Mousses souples en polyuréthane lavables et viscoélastiques |
| DE102012203639A1 (de) | 2012-03-08 | 2013-09-12 | Evonik Industries Ag | Additiv zur Einstellung der Glasübergangstemperatur von viskoelastischen Polyurethanweichschaumstoffen |
| US9320311B2 (en) | 2012-05-02 | 2016-04-26 | Intellectual Property Holdings, Llc | Helmet impact liner system |
| US9894953B2 (en) | 2012-10-04 | 2018-02-20 | Intellectual Property Holdings, Llc | Helmet retention system |
| CN104031235B (zh) | 2013-03-05 | 2016-07-13 | 万华化学（北京）有限公司 | 一种粘弹性聚氨酯吸音泡沫的制备方法 |
| US10201205B2 (en) * | 2013-03-15 | 2019-02-12 | Moor Innovative Technologies, Llc | Helmet liner |
| JP6125451B2 (ja) * | 2013-03-28 | 2017-05-10 | 三洋化成工業株式会社 | 軟質ポリウレタンフォームの製造方法 |
| USD733972S1 (en) | 2013-09-12 | 2015-07-07 | Intellectual Property Holdings, Llc | Helmet |
| EP3062650B1 (fr) | 2013-10-28 | 2019-07-03 | Intellectual Property Holdings, LLC | Système de retenue de casque |
| US11754374B2 (en) | 2014-04-01 | 2023-09-12 | University Of Tennessee Research Foundation | Energy absorbing nanocomposite materials and methods thereof |
| MX2016014167A (es) | 2014-04-30 | 2017-02-22 | Honeywell Int Inc | Espumas termoestables, de celda abierta, flexibles, y agentes de soplado, y los metodos para prepararlas. |
| RU2697514C2 (ru) * | 2014-10-07 | 2019-08-15 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Улучшения, относящиеся к полиуретанам |
| USD793625S1 (en) | 2014-10-23 | 2017-08-01 | Intellectual Property Holdings, Llc | Helmet |
| US9951174B2 (en) | 2015-05-20 | 2018-04-24 | Covestro Llc | Polyol compositions, a process for the production of these polyol compositions, and their use in the production of open celled polyurethane foams having high airflow |
| CN107849212B (zh) | 2015-07-06 | 2021-01-08 | 陶氏环球技术有限责任公司 | 聚氨酯预聚物 |
| CN109451734B (zh) * | 2016-07-21 | 2021-05-18 | 陶氏环球技术有限责任公司 | 复合缓冲结构和其制造方法 |
| US10155837B2 (en) | 2016-07-29 | 2018-12-18 | Resinate Materials Group, Inc. | Sustainable polyester polyol compositions |
| WO2018022368A1 (fr) | 2016-07-29 | 2018-02-01 | Resinate Materials Group, Inc. | Compositions de polyester-polyols durables |
| US11021567B2 (en) | 2017-03-15 | 2021-06-01 | Covestro Llc | Polyols for improved viscoelastic foams with reduced temperature sensitivity |
| US10766998B2 (en) | 2017-11-21 | 2020-09-08 | Covestro Llc | Flexible polyurethane foams |
| PL3765558T3 (pl) | 2018-03-13 | 2023-05-29 | Dow Global Technologies Llc | Pianka lepkosprężysta o powolnym czasie powrotu do stanu wyjściowego |
| CN108570138B (zh) * | 2018-03-30 | 2020-08-25 | 黎明化工研究设计院有限责任公司 | 一种高阻燃低密度低温敏性聚氨酯慢回弹泡沫 |
| US10793692B2 (en) | 2018-10-24 | 2020-10-06 | Covestro Llc | Viscoelastic flexible foams comprising hydroxyl-terminated prepolymers |
| WO2021071808A1 (fr) | 2019-10-09 | 2021-04-15 | Covestro Llc | Procédés, systèmes et progiciels informatiques pour la production de produits en mousse de polyuréthane utilisant l'imagerie optique et infrarouge |
| WO2022074500A1 (fr) | 2020-10-06 | 2022-04-14 | Toscana Gomma S.P.A. | Siège pour véhicule et sa méthode de fabrication |
| US11572433B2 (en) | 2021-03-12 | 2023-02-07 | Covestro Llc | In-situ formed polyols, a process for their preparation, foams prepared from these in-situ formed polyols and a process for their preparation |
| EP4314104A1 (fr) * | 2021-03-23 | 2024-02-07 | Covestro Deutschland AG | Procédé de réduction de (di)amines aromatiques dans des mousses de polyuréthane |
| US11718705B2 (en) | 2021-07-28 | 2023-08-08 | Covestro Llc | In-situ formed polyether polyols, a process for their preparation, and a process for the preparation of polyurethane foams |
| US20230039276A1 (en) | 2021-07-28 | 2023-02-09 | Covestro Llc | Novel polyether polyol blends, a process for their preparation, foams prepared from these polyether polyol blends and a process for their preparation |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3405077A (en) | 1964-12-31 | 1968-10-08 | Dow Chemical Co | Process for making soft polyurethane foams and product |
| US3875086A (en) | 1973-08-10 | 1975-04-01 | Jefferson Chem Co Inc | Urethane containing monohydric polyether chain stoppers |
| CA1111996A (fr) | 1978-09-20 | 1981-11-03 | Som N. Khanna | Mousse de polyurethane amortisseuse semi-souple |
| US4367259A (en) | 1981-07-27 | 1983-01-04 | W. R. Grace & Co. | Sound deadening material |
| US4722946A (en) | 1986-07-03 | 1988-02-02 | Polymer Dynamics (Delaware), Ltd. | Energy-attenuating polyurethanes |
| DE3710731A1 (de) | 1987-03-31 | 1989-04-27 | Stankiewicz Alois Dr Gmbh | Polyurethanweichschaumstoff mit schallisolierenden und entdroehnenden eigenschaften |
| JPH0284421A (ja) | 1988-06-04 | 1990-03-26 | Achilles Corp | 衝撃吸収性ポリウレタンフォーム及びその製造方法 |
| US4981880A (en) | 1988-09-23 | 1991-01-01 | The Dow Chemical Company | Process for making low density flexible polyisocyanurate-polyurethane foams |
| NZ230729A (en) * | 1988-09-23 | 1992-04-28 | Dow Chemical Co | Preparation of soft flexible polyurethane foam from a composition comprising a polyol and a monohydric polyether, in the presence of a trimerisation catalyst |
| US4950695A (en) * | 1989-03-06 | 1990-08-21 | Pmc, Inc. | Reduction of firmness in flexible polyurethane foam by addition of monofunctional alcohols, polyesters, and polyethers |
| US4980386A (en) | 1989-04-28 | 1990-12-25 | Polymer Dynamics Technology, Inc. | Methods for the manufacture of energy-attenuating polyurethanes |
| DE3942330A1 (de) | 1989-12-21 | 1991-06-27 | Basf Ag | Verfahren zur herstellung von flexiblen polyurethan-weichschaumstoffen mit viskoelastischen, koerperschalldaempfenden eigenschaften und hierzu verwendbare polyoxyalkylen-polyol-mischungen |
| JP3500700B2 (ja) | 1994-05-31 | 2004-02-23 | 旭硝子株式会社 | 非フォーム状ポリウレタン樹脂の製造方法 |
| DE4443432A1 (de) | 1994-12-06 | 1996-06-13 | Elastogran Gmbh | Unter Druck stehende, Treibmittel enthaltende Isocyanat-Semirpräpolymermischungen auf Basis von Mischungen aus Polyhydroxylverbindungen und Monoalkoholen und/oder Hydroxyketonen, ihre Verwendung zur Herstellung von Polyurethanschaumstoffen und ein Verfahren hierfür |
| DE19744747A1 (de) | 1997-10-10 | 1999-04-15 | Basf Ag | Verfahren zur Herstellung von Polyurethan-Weichschaumstoffen |
| US6136879A (en) | 1997-10-28 | 2000-10-24 | Tokai Rubber Industries, Ltd. | Soft polyurethane foam, method of producing the same and vehicle interior member using the same |
| US5919395A (en) | 1997-10-30 | 1999-07-06 | Shell Oil Company | Polyol combination |
-
2000
- 2000-01-31 US US09/495,192 patent/US6391935B1/en not_active Expired - Lifetime
-
2001
- 2001-01-24 AU AU2001230455A patent/AU2001230455A1/en not_active Abandoned
- 2001-01-24 CA CA002398507A patent/CA2398507C/fr not_active Expired - Lifetime
- 2001-01-24 MX MXPA02007351A patent/MXPA02007351A/es active IP Right Grant
- 2001-01-24 PL PL01356303A patent/PL356303A1/xx unknown
- 2001-01-24 BR BR0107957-3A patent/BR0107957A/pt not_active Application Discontinuation
- 2001-01-24 WO PCT/IB2001/000209 patent/WO2001057104A2/fr not_active Application Discontinuation
- 2001-01-24 JP JP2001557934A patent/JP2003522235A/ja active Pending
- 2001-01-24 EP EP01902598A patent/EP1268596A2/fr not_active Withdrawn
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2002
- 2002-07-18 NO NO20023453A patent/NO20023453L/no not_active Application Discontinuation
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| Publication number | Publication date |
|---|---|
| MXPA02007351A (es) | 2003-10-14 |
| WO2001057104A2 (fr) | 2001-08-09 |
| JP2003522235A (ja) | 2003-07-22 |
| AU2001230455A1 (en) | 2001-08-14 |
| US6391935B1 (en) | 2002-05-21 |
| NO20023453D0 (no) | 2002-07-18 |
| CA2398507A1 (fr) | 2001-08-09 |
| WO2001057104A3 (fr) | 2002-01-10 |
| CA2398507C (fr) | 2009-09-29 |
| BR0107957A (pt) | 2002-10-29 |
| EP1268596A2 (fr) | 2003-01-02 |
| PL356303A1 (en) | 2004-06-28 |
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