JPH057413B2 - - Google Patents
Info
- Publication number
- JPH057413B2 JPH057413B2 JP18007888A JP18007888A JPH057413B2 JP H057413 B2 JPH057413 B2 JP H057413B2 JP 18007888 A JP18007888 A JP 18007888A JP 18007888 A JP18007888 A JP 18007888A JP H057413 B2 JPH057413 B2 JP H057413B2
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- mol
- resistance
- ethylene oxide
- oil
- 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 - Fee Related
Links
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 12
- 229920000570 polyether Polymers 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 8
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 4
- 229920001971 elastomer Polymers 0.000 description 24
- 229920001577 copolymer Polymers 0.000 description 23
- 239000005060 rubber Substances 0.000 description 23
- 239000003921 oil Substances 0.000 description 17
- 239000010687 lubricating oil Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 230000007423 decrease Effects 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002685 polymerization catalyst Substances 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- OIFAHDAXIUURLN-UHFFFAOYSA-N 2-(fluoromethyl)oxirane Chemical compound FCC1CO1 OIFAHDAXIUURLN-UHFFFAOYSA-N 0.000 description 1
- AGIBHMPYXXPGAX-UHFFFAOYSA-N 2-(iodomethyl)oxirane Chemical compound ICC1CO1 AGIBHMPYXXPGAX-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- -1 Ethylene oxide-propylene oxide-epibromohydrin Chemical compound 0.000 description 1
- ZBASITASASAVOT-UHFFFAOYSA-N P(=O)(OCCCC)(OCCCC)OCCCC.C(CCC)[Sn](CCCC)=O Chemical compound P(=O)(OCCCC)(OCCCC)OCCCC.C(CCC)[Sn](CCCC)=O ZBASITASASAVOT-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 125000002370 organoaluminium group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Polyethers (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18007888A JPH0229425A (ja) | 1988-07-19 | 1988-07-19 | ポリエーテル共重合体 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18007888A JPH0229425A (ja) | 1988-07-19 | 1988-07-19 | ポリエーテル共重合体 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0229425A JPH0229425A (ja) | 1990-01-31 |
JPH057413B2 true JPH057413B2 (enrdf_load_stackoverflow) | 1993-01-28 |
Family
ID=16077072
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18007888A Granted JPH0229425A (ja) | 1988-07-19 | 1988-07-19 | ポリエーテル共重合体 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0229425A (enrdf_load_stackoverflow) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19549425A1 (de) * | 1995-09-13 | 1997-03-20 | Bayer Ag | Vernetzbare Raumtemperatur-vulkanisierende Massen |
FR2814088B1 (fr) * | 2000-09-15 | 2002-12-13 | Centre Nat Rech Scient | Membranes pour la separation selective gazeuse |
CN109762157A (zh) * | 2019-01-14 | 2019-05-17 | 蔡振云 | 一种高分子量聚氧乙烯醚的制备方法 |
-
1988
- 1988-07-19 JP JP18007888A patent/JPH0229425A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0229425A (ja) | 1990-01-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5332798A (en) | Fluorinated polyurethanes and polyurethane-ureas, and methods for preparing them | |
US3544655A (en) | Alkylene oxide copolymers with 0.01 to 2.0 percent of a polyepoxide | |
US5508380A (en) | Fluorinated polymers containing perfluoropolyoxyalkylene sequences and having thermoplastic elastomeric properties | |
Jha et al. | Thermoplastic elastomeric blends of nylon-6/acrylate rubber: influence of interaction on mechanical and dynamic mechanical thermal properties | |
Murbach et al. | Linear polyurethanes from polyalkylene ether glycols | |
US3341475A (en) | Vulcanizable copolymers of oxetanes and halogen substituted epoxides | |
JPH057413B2 (enrdf_load_stackoverflow) | ||
JPH057414B2 (enrdf_load_stackoverflow) | ||
US3917554A (en) | Butadiene-acrylonitrile alternating copolymer solution-type adhesive | |
Jong et al. | Synthesis, characterization, and rubber elasticity of end-linked poly (tetrahydrofuran) elastomer | |
Stefani et al. | Polyurethane‐ductilized epoxy resins | |
Toselli et al. | Fluorinated poly (butylene terephthalate): Preparation and properties | |
JPH0149374B2 (enrdf_load_stackoverflow) | ||
CA1210187A (en) | Rubbery solid polymer or copolymer of glycidyl carboxylate and composition thereof | |
Sathiyalekshmi et al. | Synthesis and characterisation of rigid polyurethanes based on hydroxyalkylated cardanol formaldehyde resin | |
JPS60123531A (ja) | グリシジルエステル−アリルグリシジルエ−テル−エチレン性エポキシド共重合体 | |
US3799895A (en) | Halocyanoalkyl epoxy ethers and polymers thereof | |
US3459721A (en) | Dialkylaluminum acetylacetonate polymerization catalysts | |
JP6589976B2 (ja) | 共重合体、重合体組成物及び架橋重合体 | |
US3435015A (en) | Tetrahydrofuran polymers | |
JPS63317527A (ja) | エポキシド共重合体 | |
US3728320A (en) | Polymeric epoxides | |
Mukhopadhyay et al. | Self‐vulcanizable rubber blend based on neoprene and carboxylated nitrile rubber: Effect of blend ratio on miscibility and physical properties | |
JPS6257654B2 (enrdf_load_stackoverflow) | ||
Semsarzadeh et al. | Polymerization of Three Bromo-2, 6-xylenols in THF Solution |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |