JPS60262821A - グリシジルエステル共重合体 - Google Patents
グリシジルエステル共重合体Info
- Publication number
- JPS60262821A JPS60262821A JP11874084A JP11874084A JPS60262821A JP S60262821 A JPS60262821 A JP S60262821A JP 11874084 A JP11874084 A JP 11874084A JP 11874084 A JP11874084 A JP 11874084A JP S60262821 A JPS60262821 A JP S60262821A
- Authority
- JP
- Japan
- Prior art keywords
- mol
- glycidyl ether
- copolymer
- formula
- glycidyl ester
- 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.)
- Granted
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 18
- -1 alkyl orthophosphate Chemical compound 0.000 claims abstract description 15
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 10
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 239000000178 monomer Substances 0.000 claims abstract description 6
- 239000007787 solid Substances 0.000 claims abstract description 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- 229920000570 polyether Polymers 0.000 claims abstract description 4
- 125000005843 halogen group Chemical group 0.000 claims abstract description 3
- 150000002118 epoxides Chemical class 0.000 claims abstract 2
- 241000238557 Decapoda Species 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000003944 halohydrins Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000003054 catalyst Substances 0.000 abstract description 15
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 239000007859 condensation product Substances 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 2
- 229920000388 Polyphosphate Polymers 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000001205 polyphosphate Substances 0.000 abstract 1
- 235000011176 polyphosphates Nutrition 0.000 abstract 1
- 238000007142 ring opening reaction Methods 0.000 abstract 1
- 150000004671 saturated fatty acids Chemical class 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 description 13
- 150000002924 oxiranes Chemical class 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 9
- 239000005060 rubber Substances 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical group ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 6
- JKXONPYJVWEAEL-UHFFFAOYSA-N oxiran-2-ylmethyl acetate Chemical compound CC(=O)OCC1CO1 JKXONPYJVWEAEL-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000007334 copolymerization reaction Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- ZVNYKZKUBKIIAH-UHFFFAOYSA-N 2-(oxiran-2-yl)acetic acid Chemical compound OC(=O)CC1CO1 ZVNYKZKUBKIIAH-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 210000003127 knee Anatomy 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Landscapes
- Polyethers (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11874084A JPS60262821A (ja) | 1984-06-08 | 1984-06-08 | グリシジルエステル共重合体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11874084A JPS60262821A (ja) | 1984-06-08 | 1984-06-08 | グリシジルエステル共重合体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60262821A true JPS60262821A (ja) | 1985-12-26 |
| JPH0149374B2 JPH0149374B2 (enrdf_load_stackoverflow) | 1989-10-24 |
Family
ID=14743890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11874084A Granted JPS60262821A (ja) | 1984-06-08 | 1984-06-08 | グリシジルエステル共重合体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60262821A (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103443160A (zh) * | 2011-03-15 | 2013-12-11 | 气体产品与化学公司 | 来自选择性改性胺的聚酰胺和酰胺基胺 |
| CN103917576A (zh) * | 2011-10-19 | 2014-07-09 | 迈图专业化学股份有限公司 | 聚醚多元醇树脂组合物 |
| US9663597B2 (en) | 2011-10-19 | 2017-05-30 | Hexicon Inc. | Acrylic polyol resins compositions |
| US9803051B2 (en) | 2011-10-19 | 2017-10-31 | Hexion Inc. | Acrylic polyol resins compositions |
| US9879113B2 (en) | 2010-12-22 | 2018-01-30 | Hexion Inc. | Glycidyl esters of alpha, alpha branched acids compositions |
| CN118149182A (zh) * | 2024-05-09 | 2024-06-07 | 海南中盛旭鑫低碳科技有限公司 | 一种桥联枢纽模块防腐输送管及其制备方法 |
-
1984
- 1984-06-08 JP JP11874084A patent/JPS60262821A/ja active Granted
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9879113B2 (en) | 2010-12-22 | 2018-01-30 | Hexion Inc. | Glycidyl esters of alpha, alpha branched acids compositions |
| CN103443160A (zh) * | 2011-03-15 | 2013-12-11 | 气体产品与化学公司 | 来自选择性改性胺的聚酰胺和酰胺基胺 |
| CN103917576A (zh) * | 2011-10-19 | 2014-07-09 | 迈图专业化学股份有限公司 | 聚醚多元醇树脂组合物 |
| US9663597B2 (en) | 2011-10-19 | 2017-05-30 | Hexicon Inc. | Acrylic polyol resins compositions |
| US9751982B2 (en) | 2011-10-19 | 2017-09-05 | Hexion Inc | Polyether polyol resins compositions |
| US9803051B2 (en) | 2011-10-19 | 2017-10-31 | Hexion Inc. | Acrylic polyol resins compositions |
| CN118149182A (zh) * | 2024-05-09 | 2024-06-07 | 海南中盛旭鑫低碳科技有限公司 | 一种桥联枢纽模块防腐输送管及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0149374B2 (enrdf_load_stackoverflow) | 1989-10-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0719293A1 (en) | Latent, thermal cure accelerators for epoxy-aromatic amine resins | |
| Liu et al. | Bio‐based benzoxazines based on sesamol: synthesis and properties | |
| US3544655A (en) | Alkylene oxide copolymers with 0.01 to 2.0 percent of a polyepoxide | |
| WO1989006253A1 (en) | Hydrogenated derivative of ring-opening copolymer and process for its production | |
| US3945972A (en) | Curable epoxy resin composition comprising an epoxy resin and a reactive diluent | |
| JPS60262821A (ja) | グリシジルエステル共重合体 | |
| Bouillon et al. | Influence of different imidazole catalysts on epoxy‐anhydride copolymerization and on their network properties | |
| GB2085011A (en) | Heat curable epoxy resin compositions | |
| WO1993017063A1 (en) | Crosslinkable carbosilane polymer formulations | |
| CN110078894A (zh) | 一种萘二酚型超支化环氧树脂及其制备方法和应用 | |
| Caşcaval et al. | Curing of some epoxy-acrylate glycidyl ethers based on para-alkyl substituted phenols | |
| Mas et al. | Improved thermosets obtained from cycloaliphatic epoxy resins and γ‐butyrolactone with lanthanide triflates as initiators. I. Study of curing by differential scanning calorimetry and Fourier transform infrared | |
| EP0220072A2 (en) | Method of improving flame resistance of epoxy resins and resulting compositions | |
| US3684787A (en) | Preparation of polyalkenamers | |
| 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 | |
| Cantor et al. | Synthesis and polymerization studies of cyano epoxides | |
| Giannetti et al. | Ammonium salt catalyzed crosslinking mechanism of acrylic rubbers | |
| CA1105042A (en) | Epoxy resins and process for producing the same | |
| JPS60123530A (ja) | グリシジルエステル−エピハロヒドリン−エチレン性エポキシド共重合体 | |
| JPS62225506A (ja) | イソブチレン共重合体、その製法及び用途 | |
| GB1582414A (en) | Process for the production of butadiene-propylene copolymers | |
| JPS6023423A (ja) | グリシジルエステル−エピハロヒドリン共重合体 | |
| JPS6023422A (ja) | グリシジルエステル−アリルグリシジルエ−テル共重合体 | |
| US4530994A (en) | Rubbery solid polymer or copolymer of glycidyl carboxylate and composition thereof | |
| JP7639383B2 (ja) | トリアリルイソシアヌレート重合体、その製造方法、硬化性組成物及び高分子成形体 |