DE1964998C3 - Verfahren zur Herstellung von Polyurethanelastomeren - Google Patents
Verfahren zur Herstellung von PolyurethanelastomerenInfo
- Publication number
- DE1964998C3 DE1964998C3 DE1964998A DE1964998A DE1964998C3 DE 1964998 C3 DE1964998 C3 DE 1964998C3 DE 1964998 A DE1964998 A DE 1964998A DE 1964998 A DE1964998 A DE 1964998A DE 1964998 C3 DE1964998 C3 DE 1964998C3
- Authority
- DE
- Germany
- Prior art keywords
- molecular weight
- hexanediol
- adipic acid
- polyester
- mol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000034 method Methods 0.000 title claims description 17
- 229920003225 polyurethane elastomer Polymers 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 36
- 229920000728 polyester Polymers 0.000 claims description 25
- 235000011037 adipic acid Nutrition 0.000 claims description 18
- 239000001361 adipic acid Substances 0.000 claims description 18
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 14
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 13
- -1 diaryl carbonate Chemical compound 0.000 claims description 11
- 125000005442 diisocyanate group Chemical group 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 6
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 3
- 238000005886 esterification reaction Methods 0.000 claims description 3
- 150000002513 isocyanates Chemical class 0.000 claims description 3
- 238000005809 transesterification reaction Methods 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 12
- 229920001971 elastomer Polymers 0.000 description 12
- 239000000806 elastomer Substances 0.000 description 12
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 11
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 239000004970 Chain extender Substances 0.000 description 8
- 229920000515 polycarbonate Polymers 0.000 description 7
- 239000004417 polycarbonate Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 150000002440 hydroxy compounds Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 6
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000000465 moulding Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- WPEOOEIAIFABQP-UHFFFAOYSA-N hexanedioic acid;hexane-1,6-diol Chemical compound OCCCCCCO.OC(=O)CCCCC(O)=O WPEOOEIAIFABQP-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000007493 shaping process Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 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 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- 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 1
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 230000003301 hydrolyzing effect Effects 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
- 238000002844 melting Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000004072 triols Chemical class 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
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/675—Low-molecular-weight compounds
-
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
- C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
-
- 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
- C08G2410/00—Soles
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)
- Polyesters Or Polycarbonates (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1964998A DE1964998C3 (de) | 1969-12-24 | 1969-12-24 | Verfahren zur Herstellung von Polyurethanelastomeren |
| GB54087/70A GB1270077A (en) | 1969-12-24 | 1970-11-13 | Process for the production of polyurethane elastomers |
| SE16998/70A SE366329B (enExample) | 1969-12-24 | 1970-12-15 | |
| JP45111327A JPS492358B1 (enExample) | 1969-12-24 | 1970-12-15 | |
| CA100863A CA934090A (en) | 1969-12-24 | 1970-12-16 | Process for the production of polyurethane elastomers |
| NL7018662A NL7018662A (enExample) | 1969-12-24 | 1970-12-22 | |
| BE760826A BE760826A (fr) | 1969-12-24 | 1970-12-24 | Procede de preparation d'elastomeres de |
| FR7046624A FR2074265A5 (enExample) | 1969-12-24 | 1970-12-24 | |
| US00247212A US3758443A (en) | 1969-12-24 | 1972-04-24 | Icular polyol polycarbonate process for the production of polyurethane elastomers based on a part |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1964998A DE1964998C3 (de) | 1969-12-24 | 1969-12-24 | Verfahren zur Herstellung von Polyurethanelastomeren |
| US24721272A | 1972-04-24 | 1972-04-24 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE1964998A1 DE1964998A1 (de) | 1971-07-01 |
| DE1964998B2 DE1964998B2 (de) | 1977-07-07 |
| DE1964998C3 true DE1964998C3 (de) | 1979-02-15 |
Family
ID=25758287
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1964998A Expired DE1964998C3 (de) | 1969-12-24 | 1969-12-24 | Verfahren zur Herstellung von Polyurethanelastomeren |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3758443A (enExample) |
| JP (1) | JPS492358B1 (enExample) |
| BE (1) | BE760826A (enExample) |
| CA (1) | CA934090A (enExample) |
| DE (1) | DE1964998C3 (enExample) |
| FR (1) | FR2074265A5 (enExample) |
| GB (1) | GB1270077A (enExample) |
| NL (1) | NL7018662A (enExample) |
| SE (1) | SE366329B (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4216298A (en) | 1976-11-12 | 1980-08-05 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid bis-diphenol esters of polyester-diols and their use for the preparation of high-molecular segmented polyester/polycarbonates which can be processed as thermoplastics |
| US4217437A (en) | 1977-06-11 | 1980-08-12 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid bis-diphenol esters of polyalkylene oxide-diols lengthened via carbonate groups and their use for the preparation of high-molecular, segmented polyether/polycarbonates which can be processed as thermoplastics |
| US4217297A (en) | 1977-03-22 | 1980-08-12 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups |
| US4297455A (en) | 1977-03-22 | 1981-10-27 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups and their use for the preparation of polyester-diol bis-diphenol carbonates and polyester/polycarbonates |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE29623E (en) * | 1972-05-04 | 1978-05-02 | Bayer Aktiengesellschaft | Polyurethane-ureas based on cis-trans-1,4-diaminocyclohexane |
| DE2221751C3 (de) * | 1972-05-04 | 1978-08-10 | Bayer Ag, 5090 Leverkusen | Polyurethanharnstoff elastomere |
| USRE29224E (en) * | 1972-05-04 | 1977-05-17 | Bayer Aktiengesellschaft | Polyurethane urea elastomers based on polycarbonate macrodiols |
| DE2221798C3 (de) * | 1972-05-04 | 1978-07-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyurethanharnstoff-Lösungen |
| JPS50119675A (enExample) * | 1974-03-04 | 1975-09-19 | ||
| DE2651639A1 (de) * | 1976-11-12 | 1978-05-24 | Bayer Ag | Verfahren zur herstellung von kohlensaeureestern von polyesterpolyolen |
| DE2732718A1 (de) * | 1977-07-20 | 1979-02-15 | Bayer Ag | Carbonatgruppen enthaltende polyester |
| EP0004020B1 (de) | 1978-03-10 | 1981-07-15 | Bayer Ag | Polycarbonat-Formmassen mit verbesserten zähelastischen Eigenschaften |
| US4267120A (en) * | 1979-12-14 | 1981-05-12 | Texaco Development Corp. | Polyester polycarbonates |
| BR8001404A (pt) * | 1980-03-10 | 1981-09-15 | Torrington Co | Cinta anular de retencao de arruela axial armacao para cortinas, aplicavel em boxes |
| DE3219156A1 (de) * | 1982-05-21 | 1983-11-24 | Kaco Gmbh Co | Dichtung fuer waelz- und/oder gleitlager |
| US4456745A (en) * | 1982-05-24 | 1984-06-26 | Ethyl Corporation | Polyurethanes prepared from polycarbonates |
| US4423205A (en) * | 1982-05-24 | 1983-12-27 | Ethyl Corporation | Cationic polymerization of cyclic carbonates |
| DE3717060A1 (de) * | 1987-05-21 | 1988-12-01 | Bayer Ag | Polyether-polycarbonat-diole, ihre herstellung und verwendung als ausgangsprodukte fuer polyurethankunststoffe |
| US4916207A (en) * | 1987-12-17 | 1990-04-10 | Allied-Signal, Inc. | Polycarbonate homopolymer-based fiber compositions and method of melt-spinning same and device |
| US4891263A (en) * | 1987-12-17 | 1990-01-02 | Allied-Signal Inc. | Polycarbonate random copolymer-based fiber compositions and method of melt-spinning same and device |
| US4916193A (en) * | 1987-12-17 | 1990-04-10 | Allied-Signal Inc. | Medical devices fabricated totally or in part from copolymers of recurring units derived from cyclic carbonates and lactides |
| US5145945A (en) * | 1987-12-17 | 1992-09-08 | Allied-Signal Inc. | Homopolymers and copolymers having recurring carbonate units |
| US5120802A (en) * | 1987-12-17 | 1992-06-09 | Allied-Signal Inc. | Polycarbonate-based block copolymers and devices |
| US5256764A (en) * | 1987-12-17 | 1993-10-26 | United States Surgical Corporation | Medical devices fabricated from homopolymers and copolymers having recurring carbonate units |
| US5274074A (en) * | 1987-12-17 | 1993-12-28 | United States Surgical Corporation | Medical devices fabricated from homopolymers and copolymers having recurring carbonate units |
| US5152781A (en) * | 1987-12-17 | 1992-10-06 | Allied-Signal Inc. | Medical devices fabricated from homopolymers and copolymers having recurring carbonate units |
| IT1227136B (it) * | 1988-10-14 | 1991-03-19 | Enichem Sintesi | Policarbonati copoliesteri dioli, procedimento per la loro produzione e loro impiego. |
| US5096992A (en) * | 1989-03-20 | 1992-03-17 | Reeves Brothers, Inc. | Use of modified diisocyanates for preparing linear thermoplastic polyurethane elastomers having improved properties |
| US5298303A (en) * | 1989-03-20 | 1994-03-29 | Reeves Brothers, Inc. | Fabric structure for severe use applications |
| US5001208A (en) * | 1989-03-20 | 1991-03-19 | Reeves Brothers, Inc. | Linear polyurethane elastomer compositions based on mixed polycarbonate and polyether polyols |
| US5130384A (en) * | 1989-03-20 | 1992-07-14 | Reeves Brothers, Inc. | Calenderable thermoplastic polyurethane elastomer compositions containing millable linear polyurethanes |
| DE3932949A1 (de) * | 1989-10-03 | 1991-04-11 | Bayer Ag | Elasthanfasern hoher dehnbarkeit und festigkeit und ein verfahren zu ihrer herstellung |
| CA2037606C (en) * | 1990-03-13 | 2002-06-04 | Yukiatsu Komiya | Polyurethane, elastic polyurethane fiber and polyesterpolycarbonatediol used for the same |
| US5110666A (en) * | 1991-05-06 | 1992-05-05 | Reeves Brothers, Inc. | Coated fabric structure for air bag applications |
| JPH07211584A (ja) * | 1994-01-17 | 1995-08-11 | Diafoil Co Ltd | 金属蒸着ポリエステルフィルムコンデンサ |
| DE19513164A1 (de) * | 1995-04-07 | 1996-10-10 | Bayer Ag | Polycarbonat-Diole, ihre Herstellung und Verwendung als Ausgangsprodukte für Polyurethan-Kunststoffe |
| DE19819847A1 (de) * | 1998-05-05 | 1999-11-11 | Spindelfabrik Neudorf Gmbh | Lagerbuchse für die Umhüllung der Lagerringe von Wälzlagern an Textilspindeln |
| DE10303881A1 (de) | 2003-01-31 | 2004-08-12 | Bayer Ag | Verfahren zur Herstellung von oligomeren aliphatischen Diolen, darauf basierenden Polycarbonatdiolen und deren Prepolymeren |
| DE102005011448A1 (de) * | 2005-03-12 | 2006-09-21 | Bayer Materialscience Ag | Poly(urethancarbonat)polyole |
| JP4798156B2 (ja) * | 2008-03-17 | 2011-10-19 | 三菱樹脂株式会社 | 積層フィルム |
| CN115044029B (zh) * | 2021-03-08 | 2024-12-03 | 旭化成株式会社 | 聚酯聚碳酸酯多元醇和合成皮革 |
-
1969
- 1969-12-24 DE DE1964998A patent/DE1964998C3/de not_active Expired
-
1970
- 1970-11-13 GB GB54087/70A patent/GB1270077A/en not_active Expired
- 1970-12-15 SE SE16998/70A patent/SE366329B/xx unknown
- 1970-12-15 JP JP45111327A patent/JPS492358B1/ja active Pending
- 1970-12-16 CA CA100863A patent/CA934090A/en not_active Expired
- 1970-12-22 NL NL7018662A patent/NL7018662A/xx unknown
- 1970-12-24 BE BE760826A patent/BE760826A/xx not_active IP Right Cessation
- 1970-12-24 FR FR7046624A patent/FR2074265A5/fr not_active Expired
-
1972
- 1972-04-24 US US00247212A patent/US3758443A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4216298A (en) | 1976-11-12 | 1980-08-05 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid bis-diphenol esters of polyester-diols and their use for the preparation of high-molecular segmented polyester/polycarbonates which can be processed as thermoplastics |
| US4217297A (en) | 1977-03-22 | 1980-08-12 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups |
| US4297455A (en) | 1977-03-22 | 1981-10-27 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid aryl esters of polyester-diols lengthened via carbonate groups and their use for the preparation of polyester-diol bis-diphenol carbonates and polyester/polycarbonates |
| US4217437A (en) | 1977-06-11 | 1980-08-12 | Bayer Aktiengesellschaft | Process for the preparation of carbonic acid bis-diphenol esters of polyalkylene oxide-diols lengthened via carbonate groups and their use for the preparation of high-molecular, segmented polyether/polycarbonates which can be processed as thermoplastics |
Also Published As
| Publication number | Publication date |
|---|---|
| SE366329B (enExample) | 1974-04-22 |
| DE1964998B2 (de) | 1977-07-07 |
| FR2074265A5 (enExample) | 1971-10-01 |
| JPS492358B1 (enExample) | 1974-01-19 |
| NL7018662A (enExample) | 1971-06-28 |
| BE760826A (fr) | 1971-05-27 |
| DE1964998A1 (de) | 1971-07-01 |
| CA934090A (en) | 1973-09-18 |
| GB1270077A (en) | 1972-04-12 |
| US3758443A (en) | 1973-09-11 |
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| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |