RU2703620C2 - Полимерная композиция, способ ее получения, ее применение и содержащая ее композиция - Google Patents
Полимерная композиция, способ ее получения, ее применение и содержащая ее композиция Download PDFInfo
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- RU2703620C2 RU2703620C2 RU2017126036A RU2017126036A RU2703620C2 RU 2703620 C2 RU2703620 C2 RU 2703620C2 RU 2017126036 A RU2017126036 A RU 2017126036A RU 2017126036 A RU2017126036 A RU 2017126036A RU 2703620 C2 RU2703620 C2 RU 2703620C2
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- Prior art keywords
- polymer
- epoxy resin
- composition
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- 229920000642 polymer Polymers 0.000 title claims abstract description 275
- 239000000203 mixture Substances 0.000 title claims abstract description 127
- 238000004519 manufacturing process Methods 0.000 title description 23
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 140
- 239000003822 epoxy resin Substances 0.000 claims abstract description 137
- 239000007787 solid Substances 0.000 claims abstract description 47
- 230000009477 glass transition Effects 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 27
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 22
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- 238000001694 spray drying Methods 0.000 claims abstract description 7
- 230000015271 coagulation Effects 0.000 claims abstract description 6
- 238000005345 coagulation Methods 0.000 claims abstract description 6
- 239000012798 spherical particle Substances 0.000 claims abstract description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 73
- 239000002245 particle Substances 0.000 claims description 53
- 239000012071 phase Substances 0.000 claims description 29
- 239000000843 powder Substances 0.000 claims description 28
- 239000006185 dispersion Substances 0.000 claims description 16
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 11
- 150000002170 ethers Chemical class 0.000 claims description 11
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 claims description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- 229920003986 novolac Polymers 0.000 claims description 8
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 239000008346 aqueous phase Substances 0.000 claims description 6
- CXXSQMDHHYTRKY-UHFFFAOYSA-N 4-amino-2,3,5-tris(oxiran-2-ylmethyl)phenol Chemical compound C1=C(O)C(CC2OC2)=C(CC2OC2)C(N)=C1CC1CO1 CXXSQMDHHYTRKY-UHFFFAOYSA-N 0.000 claims description 5
- 239000002612 dispersion medium Substances 0.000 claims description 5
- KGSFMPRFQVLGTJ-UHFFFAOYSA-N 1,1,2-triphenylethylbenzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 KGSFMPRFQVLGTJ-UHFFFAOYSA-N 0.000 claims description 4
- UUODQIKUTGWMPT-UHFFFAOYSA-N 2-fluoro-5-(trifluoromethyl)pyridine Chemical compound FC1=CC=C(C(F)(F)F)C=N1 UUODQIKUTGWMPT-UHFFFAOYSA-N 0.000 claims description 4
- RDIGYBZNNOGMHU-UHFFFAOYSA-N 3-amino-2,4,5-tris(oxiran-2-ylmethyl)phenol Chemical compound OC1=CC(CC2OC2)=C(CC2OC2)C(N)=C1CC1CO1 RDIGYBZNNOGMHU-UHFFFAOYSA-N 0.000 claims description 4
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 4
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- 229920002379 silicone rubber Polymers 0.000 claims description 3
- 239000004945 silicone rubber Substances 0.000 claims description 3
- 239000008247 solid mixture Substances 0.000 claims description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract description 14
- 238000009826 distribution Methods 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 description 39
- 239000010410 layer Substances 0.000 description 17
- 239000004593 Epoxy Substances 0.000 description 16
- 229920001971 elastomer Polymers 0.000 description 9
- 229920000058 polyacrylate Polymers 0.000 description 9
- 239000011258 core-shell material Substances 0.000 description 8
- 238000004630 atomic force microscopy Methods 0.000 description 7
- 230000008901 benefit Effects 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 238000007720 emulsion polymerization reaction Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- -1 cycloaliphatic Chemical group 0.000 description 6
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000004816 latex Substances 0.000 description 5
- 229920000126 latex Polymers 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 5
- 238000000399 optical microscopy Methods 0.000 description 5
- 238000009827 uniform distribution Methods 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 239000004609 Impact Modifier Substances 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 125000005250 alkyl acrylate group Chemical group 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 239000011164 primary particle Substances 0.000 description 4
- 230000000930 thermomechanical effect Effects 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 241000519995 Stachys sylvatica Species 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010556 emulsion polymerization method Methods 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000000386 microscopy Methods 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000003921 particle size analysis Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2451/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
- C08J2451/04—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2451/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
- C08J2451/06—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2463/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Dispersion Chemistry (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1463304 | 2014-12-24 | ||
| FR1463304A FR3031109B1 (fr) | 2014-12-24 | 2014-12-24 | Composition de polymeres, son procede de preparation, son utilisation et composition la comprenant |
| PCT/EP2015/081142 WO2016102658A1 (en) | 2014-12-24 | 2015-12-23 | Polymer composition, its method of preparation, its use and composition comprising it |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| RU2017126036A RU2017126036A (ru) | 2019-01-24 |
| RU2017126036A3 RU2017126036A3 (enExample) | 2019-05-16 |
| RU2703620C2 true RU2703620C2 (ru) | 2019-10-21 |
Family
ID=53514225
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2017126036A RU2703620C2 (ru) | 2014-12-24 | 2015-12-23 | Полимерная композиция, способ ее получения, ее применение и содержащая ее композиция |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10597499B2 (enExample) |
| EP (1) | EP3237501B1 (enExample) |
| JP (1) | JP7133312B2 (enExample) |
| KR (1) | KR102477079B1 (enExample) |
| CN (1) | CN107250266B (enExample) |
| BR (1) | BR112017013703B1 (enExample) |
| FR (1) | FR3031109B1 (enExample) |
| MY (1) | MY185543A (enExample) |
| RU (1) | RU2703620C2 (enExample) |
| SG (1) | SG11201705085UA (enExample) |
| WO (1) | WO2016102658A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2839050C1 (ru) * | 2020-08-17 | 2025-04-25 | ХАНТСМАН ЭДВАНСТ МАТИРИАЛЗ АМЕРИКАС ЭлЭлСи | Композиции термореактивных смол |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10259937B2 (en) * | 2014-10-29 | 2019-04-16 | Kaneka Corporation | Resin-modifying particles and vinyl chloride resin composition containing same |
| EP3547028A1 (fr) * | 2018-03-28 | 2019-10-02 | Mimotec S.A. | Methode de preparation de resine photosensible seche et resine photosensible obtenue par la methode |
| EP3778765B1 (en) * | 2018-03-30 | 2024-08-28 | Kaneka Corporation | Powder/granular material having improved dispersibility in thermosetting matrix resin |
| WO2020138263A1 (ja) | 2018-12-27 | 2020-07-02 | 株式会社カネカ | 樹脂組成物およびその利用 |
| EP4036134A4 (en) | 2019-09-27 | 2023-10-11 | Kaneka Corporation | POWDER AND METHOD FOR MANUFACTURING POWDER |
| CA3189331A1 (en) * | 2020-08-17 | 2022-02-24 | Huntsman Advanced Materials Americas Llc | Thermoset resin compositions |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1632533A1 (en) * | 2003-06-09 | 2006-03-08 | Kaneka Corporation | Process for producing modified epoxy resin |
| EP1724299A1 (en) * | 2004-02-16 | 2006-11-22 | Mitsubishi Rayon Co., Ltd. | Modifier for resin and resin composition using the same and formed article |
| WO2007025007A1 (en) * | 2005-08-24 | 2007-03-01 | Henkel Kommanditgesellschaft Auf Aktien | Epoxy compositions having improved impact resistance |
| FR2934866A1 (fr) * | 2008-08-05 | 2010-02-12 | Arkema France | Particules de type "coeur-ecorce" comprenant une ecorce a base de monomeres hydrophiles. |
| US20130115442A1 (en) * | 2011-11-09 | 2013-05-09 | Cytec Technology Corp. | Structural adhesive and bonding application thereof |
| RU2491309C2 (ru) * | 2007-11-14 | 2013-08-27 | Зика Текнолоджи Аг | Термоотверждаемые композиции на основе эпоксидных смол, содержащие неароматические мочевины в качестве ускорителей |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3674902D1 (de) * | 1985-06-26 | 1990-11-15 | Dow Chemical Co | Mit rubber modifizierte epoxyzusammensetzungen. |
| DE59310074D1 (de) * | 1992-07-09 | 2000-08-17 | Ciba Sc Holding Ag | Härtbare Suspensionen auf Basis von Epoxidharzen |
| JP3365065B2 (ja) * | 1994-08-09 | 2003-01-08 | 松下電工株式会社 | 封止用エポキシ樹脂組成物 |
| JPH09263066A (ja) * | 1996-03-27 | 1997-10-07 | Toppan Printing Co Ltd | 熱転写記録媒体及び、それを用いて製造した画像記録体 |
| DE19746006A1 (de) | 1997-10-20 | 1999-04-22 | Agomer Gmbh | Schäumbare Polyvinylhalogenidharzmassen, Verwendung von Polymerisaten darin als Verarbeitungshilfsmittel, daraus hergestellte Formteile |
| AU774649B2 (en) | 1998-10-21 | 2004-07-01 | Kitasato Daiichi Sankyo Vaccine Co.,Ltd. | Vaccine preparations containing attenuated toxin |
| US6313221B1 (en) * | 1999-05-28 | 2001-11-06 | Nippon Paint Co., Ltd. | Powder coating of epoxy-acrylic resin, polycarboxylic acid, crosslinked particles and liquid resin |
| US7485680B2 (en) | 2003-09-18 | 2009-02-03 | Kaneka Corporation | Process for producing rubbery polymer particle and process for producing resin composition containing the same |
| JP5027509B2 (ja) * | 2004-08-18 | 2012-09-19 | 株式会社カネカ | 半導体封止剤用エポキシ樹脂組成物およびエポキシ樹脂成形材料 |
| JP2007146150A (ja) * | 2005-11-02 | 2007-06-14 | Hitachi Chem Co Ltd | 封止用エポキシ樹脂組成物及びそれを用いた電子部品装置 |
| JP5409373B2 (ja) * | 2006-11-13 | 2014-02-05 | ヘンケル コーポレイション | コア−シェルゴムを有するベンゾキサジン組成物 |
| EP2123711B1 (en) * | 2007-02-28 | 2016-12-14 | Kaneka Corporation | Thermosetting resin composition having rubbery polymer particle dispersed therein, and process for production thereof |
| JP2008235669A (ja) * | 2007-03-22 | 2008-10-02 | Shin Etsu Chem Co Ltd | 半導体装置及びその製造方法 |
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- 2015-12-23 EP EP15820161.6A patent/EP3237501B1/en active Active
- 2015-12-23 JP JP2017534198A patent/JP7133312B2/ja active Active
- 2015-12-23 US US15/536,168 patent/US10597499B2/en active Active
- 2015-12-23 CN CN201580076837.7A patent/CN107250266B/zh active Active
- 2015-12-23 SG SG11201705085UA patent/SG11201705085UA/en unknown
- 2015-12-23 RU RU2017126036A patent/RU2703620C2/ru active
- 2015-12-23 MY MYPI2017000946A patent/MY185543A/en unknown
- 2015-12-23 WO PCT/EP2015/081142 patent/WO2016102658A1/en not_active Ceased
- 2015-12-23 KR KR1020177020410A patent/KR102477079B1/ko active Active
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| RU2839050C1 (ru) * | 2020-08-17 | 2025-04-25 | ХАНТСМАН ЭДВАНСТ МАТИРИАЛЗ АМЕРИКАС ЭлЭлСи | Композиции термореактивных смол |
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| Publication number | Publication date |
|---|---|
| WO2016102658A1 (en) | 2016-06-30 |
| FR3031109A1 (enExample) | 2016-07-01 |
| EP3237501A1 (en) | 2017-11-01 |
| US20170362395A1 (en) | 2017-12-21 |
| KR20170101254A (ko) | 2017-09-05 |
| US10597499B2 (en) | 2020-03-24 |
| JP2018500439A (ja) | 2018-01-11 |
| BR112017013703A2 (pt) | 2018-03-13 |
| JP7133312B2 (ja) | 2022-09-08 |
| FR3031109B1 (fr) | 2018-08-17 |
| MY185543A (en) | 2021-05-19 |
| BR112017013703B1 (pt) | 2022-02-01 |
| CN107250266B (zh) | 2021-10-29 |
| SG11201705085UA (en) | 2017-07-28 |
| RU2017126036A (ru) | 2019-01-24 |
| KR102477079B1 (ko) | 2022-12-12 |
| RU2017126036A3 (enExample) | 2019-05-16 |
| CN107250266A (zh) | 2017-10-13 |
| EP3237501B1 (en) | 2021-07-21 |
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