JPS6352045B2 - - Google Patents
Info
- Publication number
- JPS6352045B2 JPS6352045B2 JP58242180A JP24218083A JPS6352045B2 JP S6352045 B2 JPS6352045 B2 JP S6352045B2 JP 58242180 A JP58242180 A JP 58242180A JP 24218083 A JP24218083 A JP 24218083A JP S6352045 B2 JPS6352045 B2 JP S6352045B2
- Authority
- JP
- Japan
- Prior art keywords
- molecular weight
- oxide
- polyurethane elastomer
- polyoxytetramethylene glycol
- polyether diol
- 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
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 51
- -1 polyoxytetramethylene Polymers 0.000 claims description 38
- 229920003225 polyurethane elastomer Polymers 0.000 claims description 28
- 229920005862 polyol Polymers 0.000 claims description 25
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 24
- 150000003077 polyols Chemical class 0.000 claims description 24
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 22
- 150000002009 diols Chemical class 0.000 claims description 22
- 229920000570 polyether Polymers 0.000 claims description 22
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 19
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000006353 oxyethylene group Chemical group 0.000 claims description 7
- 229920001228 polyisocyanate Polymers 0.000 claims description 7
- 239000005056 polyisocyanate Substances 0.000 claims description 7
- 239000002994 raw material Substances 0.000 claims description 6
- 239000004970 Chain extender Substances 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 description 16
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000007259 addition reaction Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000004984 aromatic diamines Chemical class 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920006311 Urethane elastomer Polymers 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 239000005336 safety glass Substances 0.000 description 2
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- 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
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- PQXKWPLDPFFDJP-UHFFFAOYSA-N 2,3-dimethyloxirane Chemical compound CC1OC1C PQXKWPLDPFFDJP-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
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- GKGXKPRVOZNVPQ-UHFFFAOYSA-N diisocyanatomethylcyclohexane Chemical compound O=C=NC(N=C=O)C1CCCCC1 GKGXKPRVOZNVPQ-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- XJRAOMZCVTUHFI-UHFFFAOYSA-N isocyanic acid;methane Chemical compound C.N=C=O.N=C=O XJRAOMZCVTUHFI-UHFFFAOYSA-N 0.000 description 1
- 239000005340 laminated glass Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 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 1
Landscapes
- Polyurethanes Or Polyureas (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58242180A JPS60135421A (ja) | 1983-12-23 | 1983-12-23 | ポリウレタン系エラストマ−の製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58242180A JPS60135421A (ja) | 1983-12-23 | 1983-12-23 | ポリウレタン系エラストマ−の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60135421A JPS60135421A (ja) | 1985-07-18 |
| JPS6352045B2 true JPS6352045B2 (no) | 1988-10-17 |
Family
ID=17085496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58242180A Granted JPS60135421A (ja) | 1983-12-23 | 1983-12-23 | ポリウレタン系エラストマ−の製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60135421A (no) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4621113A (en) * | 1985-10-07 | 1986-11-04 | The Dow Chemical Company | Repeating block, oligomer-free, polyphase, thermoformable polyurethanes and method of preparation thereof |
| JPH0793778B2 (ja) * | 1988-02-25 | 1995-10-09 | 日立電線株式会社 | ケーブルシース接続工法 |
| FR2797450B1 (fr) * | 1999-08-12 | 2002-12-06 | Inst Francais Du Petrole | Derives de polytetrahydrofuranne utilisables dans des compositions detergentes pour carburants de type essence |
| CZ297662B6 (cs) | 2001-05-21 | 2007-02-28 | Huntsman International Llc | Velmi mekký polyurethanový elastomer |
| WO2006043569A1 (ja) * | 2004-10-21 | 2006-04-27 | Asahi Glass Company, Limited | ポリウレタン樹脂およびポリウレタン樹脂溶液の製造方法 |
| JP4604807B2 (ja) * | 2005-04-14 | 2011-01-05 | 旭硝子株式会社 | スキン付きポリウレタンフォーム成形品およびその製造方法 |
| US8637629B2 (en) | 2007-01-18 | 2014-01-28 | Lubrizol Advanced Materials, Inc. | High moisture vapor transmissive polyurethanes |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5450100A (en) * | 1977-09-06 | 1979-04-19 | Du Pont | Polyether*urethane polymer |
-
1983
- 1983-12-23 JP JP58242180A patent/JPS60135421A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5450100A (en) * | 1977-09-06 | 1979-04-19 | Du Pont | Polyether*urethane polymer |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60135421A (ja) | 1985-07-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4242468A (en) | Use of monohydroxylated polybutadiene as a reactive plasticizer in polyurethanes | |
| JP3097854B2 (ja) | ポリウレタン類の製造方法 | |
| AU2008200020B2 (en) | Polyurethanes cured with amines and their preparation | |
| WO1993019110A1 (en) | Thermoplastic polyurethane elastomers and polyurea elastomers | |
| JPH021842B2 (no) | ||
| EP3632958B1 (en) | Method for producing a biopolyether polyol, biopolyether polyol, and biopolyurethane resin | |
| WO2008033224A1 (en) | Isocyanate terminated polycaprolactone polyurethane prepolymers | |
| CA2523398A1 (en) | Flexible foams with low bulk densities and compressive strengths | |
| EP0556758A2 (en) | Process for producing polyurethane elastomers | |
| CA2618053A1 (en) | Polyurethanes cured with amines and their preparation | |
| JPS6352045B2 (no) | ||
| JP3613957B2 (ja) | 軟質ポリウレタンフォームの製造方法 | |
| CA1172009A (en) | Reinforced reaction injection molded elastomers | |
| KR19990083197A (ko) | 열가소성 폴리우레탄의 제법 | |
| EP0156950B1 (en) | A polyether derivative, a process for preparing the polyether derivative, a poly(urethane)ureamide obtained therefrom and a process for preparing the poly(urethane)ureamide | |
| JP7072344B2 (ja) | ポリウレタン形成性組成物 | |
| JPH11171963A (ja) | 軟質ポリウレタンフォームの製造方法 | |
| JP2002322236A (ja) | 軟質ポリウレタンスラブフォームの製造方法 | |
| US4814411A (en) | Increased reactivity of isocyanate terminated polyether prepolymers with metal halide salt complexes of methylenedianiline | |
| JPS6352046B2 (no) | ||
| JP3937811B2 (ja) | 軟質ポリウレタンフォームの製造方法 | |
| JP2592057B2 (ja) | 軟質ポリウレタンフオームの製造方法 | |
| JPH0156088B2 (no) | ||
| JPH02263818A (ja) | 新規なポリウレタンエラストマー | |
| JPH0446967B2 (no) |