BR112017013703B1 - Composição de polímero, seu método de preparação, seu uso e composição compreendendo a mesma - Google Patents
Composição de polímero, seu método de preparação, seu uso e composição compreendendo a mesma Download PDFInfo
- Publication number
- BR112017013703B1 BR112017013703B1 BR112017013703-8A BR112017013703A BR112017013703B1 BR 112017013703 B1 BR112017013703 B1 BR 112017013703B1 BR 112017013703 A BR112017013703 A BR 112017013703A BR 112017013703 B1 BR112017013703 B1 BR 112017013703B1
- Authority
- BR
- Brazil
- Prior art keywords
- polymer
- epoxy resin
- multistage
- polymer composition
- composition
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 280
- 239000000203 mixture Substances 0.000 title claims abstract description 123
- 238000000034 method Methods 0.000 title claims description 46
- 238000002360 preparation method Methods 0.000 title description 2
- 239000003822 epoxy resin Substances 0.000 claims abstract description 118
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 118
- 239000012141 concentrate Substances 0.000 claims abstract description 20
- 239000000945 filler Substances 0.000 claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 230000015271 coagulation Effects 0.000 claims abstract description 6
- 238000005345 coagulation Methods 0.000 claims abstract description 6
- 238000001694 spray drying Methods 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims description 50
- 239000007787 solid Substances 0.000 claims description 46
- 230000009477 glass transition Effects 0.000 claims description 39
- 239000004593 Epoxy Substances 0.000 claims description 29
- 239000000843 powder Substances 0.000 claims description 28
- 239000006185 dispersion Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 229920001187 thermosetting polymer Polymers 0.000 claims description 16
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 11
- 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
- 239000012071 phase Substances 0.000 claims description 9
- 239000007771 core particle Substances 0.000 claims description 7
- 239000010420 shell particle Substances 0.000 claims description 7
- 239000008346 aqueous phase Substances 0.000 claims description 6
- 125000000524 functional group Chemical group 0.000 claims description 4
- 125000005395 methacrylic acid group Chemical group 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 3
- 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 3
- 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 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 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
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
- 239000000178 monomer Substances 0.000 description 39
- 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 description 15
- 229920001971 elastomer Polymers 0.000 description 11
- 238000009826 distribution Methods 0.000 description 10
- 238000007720 emulsion polymerization reaction Methods 0.000 description 9
- 229920000058 polyacrylate Polymers 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 8
- 238000004630 atomic force microscopy Methods 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 7
- -1 cycloaliphatic Chemical group 0.000 description 6
- 239000004634 thermosetting polymer Substances 0.000 description 6
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- 238000004458 analytical method Methods 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
- 238000000399 optical microscopy 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
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 239000004971 Cross linker Substances 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
- 150000002170 ethers Chemical class 0.000 description 4
- 238000000386 microscopy Methods 0.000 description 4
- 229920003986 novolac Polymers 0.000 description 4
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 4
- 230000000930 thermomechanical effect Effects 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 239000007788 liquid Substances 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
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 239000011164 primary particle Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 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 description 2
- 229940018563 3-aminophenol Drugs 0.000 description 2
- PHZREHARUPHHCU-UHFFFAOYSA-N 4-methylbenzene-1,2,3-triol Chemical compound CC1=CC=C(O)C(O)=C1O PHZREHARUPHHCU-UHFFFAOYSA-N 0.000 description 2
- 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
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 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
- 125000005250 alkyl acrylate group Chemical group 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
- 229920001400 block copolymer Polymers 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005516 engineering process 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
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000003039 volatile agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FAUAZXVRLVIARB-UHFFFAOYSA-N 4-[[4-[bis(oxiran-2-ylmethyl)amino]phenyl]methyl]-n,n-bis(oxiran-2-ylmethyl)aniline Chemical compound C1OC1CN(C=1C=CC(CC=2C=CC(=CC=2)N(CC2OC2)CC2OC2)=CC=1)CC1CO1 FAUAZXVRLVIARB-UHFFFAOYSA-N 0.000 description 1
- 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
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 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
- 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
- 238000010008 shearing Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000003786 synthesis reaction Methods 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
- 238000012876 topography Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
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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)
- Graft Or Block Polymers (AREA)
- Dispersion Chemistry (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 (2)
| Publication Number | Publication Date |
|---|---|
| BR112017013703A2 BR112017013703A2 (pt) | 2018-03-13 |
| BR112017013703B1 true BR112017013703B1 (pt) | 2022-02-01 |
Family
ID=53514225
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112017013703-8A BR112017013703B1 (pt) | 2014-12-24 | 2015-12-23 | Composição de polímero, seu método de preparação, seu uso e composição compreendendo a mesma |
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) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016068239A1 (ja) * | 2014-10-29 | 2016-05-06 | 株式会社カネカ | 樹脂改質用粒子、及びそれを含む塩化ビニル系樹脂組成物 |
| 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 |
| CN111936574B (zh) * | 2018-03-30 | 2023-12-29 | 株式会社钟化 | 相对于热固化性基质树脂的分散性得以改善了的粉粒体 |
| EP3904453B1 (en) | 2018-12-27 | 2023-05-10 | Kaneka Corporation | Resin composition and use for same |
| WO2021060482A1 (ja) | 2019-09-27 | 2021-04-01 | 株式会社カネカ | 粉粒体および粉粒体の製造方法 |
| KR20230052295A (ko) * | 2020-08-17 | 2023-04-19 | 헌츠만 어드밴스드 머티리얼스 아메리카스 엘엘씨 | 열경화성 수지 조성물 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU574932B2 (en) * | 1985-06-26 | 1988-07-14 | Dow Chemical Company, The | Rubber-modified epoxy compounds |
| ES2148213T3 (es) * | 1992-07-09 | 2000-10-16 | Vantico Ag | Suspensiones endurecibles a base de resinas epoxi. |
| 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 |
| EP1123711B9 (en) | 1998-10-21 | 2009-08-12 | The Kitasato Institute | Attenuated toxins as adjuvants |
| 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 |
| CA2526461C (en) * | 2003-06-09 | 2013-03-19 | Kaneka Corporation | Process for producing modified epoxy resin |
| AU2004274270A1 (en) | 2003-09-18 | 2005-03-31 | Kaneka Corporation | Process for producing rubbery polymer particle and process for producing resin composition containing the same |
| EP1724299B1 (en) * | 2004-02-16 | 2011-05-18 | Mitsubishi Rayon Co., Ltd. | Modifier for resin and resin composition using the same and formed article |
| 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 |
| JP5307544B2 (ja) * | 2005-08-24 | 2013-10-02 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | 改善された耐衝撃性を有するエポキシ組成物 |
| 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 |
| CA2669040C (en) * | 2006-11-13 | 2014-10-07 | Henkel Corporation | Benzoxazine compositions with core shell rubbers |
| US8217098B2 (en) * | 2007-02-28 | 2012-07-10 | 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 |
| JP4966123B2 (ja) * | 2007-07-26 | 2012-07-04 | パナソニック株式会社 | 封止用液状エポキシ樹脂組成物および半導体装置 |
| DE502007002766D1 (de) * | 2007-11-14 | 2010-03-18 | Sika Technology Ag | Hitzehärtende Epoxidharzzusammensetzung enthaltend nichtaromatische Harnstoffe als Beschleuniger |
| US8217089B2 (en) | 2007-11-30 | 2012-07-10 | Synztec Co., Ltd. | Elastomer porous material and method of producing the same |
| FR2934866B1 (fr) * | 2008-08-05 | 2012-12-28 | Arkema France | Particules de type "coeur-ecorce" comprenant une ecorce a base de monomeres hydrophiles. |
| US8895148B2 (en) * | 2011-11-09 | 2014-11-25 | Cytec Technology Corp. | Structural adhesive and bonding application thereof |
| EP2934866B1 (de) | 2012-12-21 | 2020-10-14 | Dieffenbacher GmbH Maschinen- und Anlagenbau | Verfahren für die herstellung komplexer geometrischer strukturen aus mehreren formteilen |
-
2014
- 2014-12-24 FR FR1463304A patent/FR3031109B1/fr active Active
-
2015
- 2015-12-23 RU RU2017126036A patent/RU2703620C2/ru active
- 2015-12-23 BR BR112017013703-8A patent/BR112017013703B1/pt active IP Right Grant
- 2015-12-23 SG SG11201705085UA patent/SG11201705085UA/en unknown
- 2015-12-23 WO PCT/EP2015/081142 patent/WO2016102658A1/en not_active Ceased
- 2015-12-23 US US15/536,168 patent/US10597499B2/en active Active
- 2015-12-23 EP EP15820161.6A patent/EP3237501B1/en active Active
- 2015-12-23 KR KR1020177020410A patent/KR102477079B1/ko active Active
- 2015-12-23 JP JP2017534198A patent/JP7133312B2/ja active Active
- 2015-12-23 MY MYPI2017000946A patent/MY185543A/en unknown
- 2015-12-23 CN CN201580076837.7A patent/CN107250266B/zh active Active
Also Published As
| Publication number | Publication date |
|---|---|
| FR3031109B1 (fr) | 2018-08-17 |
| RU2703620C2 (ru) | 2019-10-21 |
| EP3237501B1 (en) | 2021-07-21 |
| CN107250266A (zh) | 2017-10-13 |
| RU2017126036A (ru) | 2019-01-24 |
| BR112017013703A2 (pt) | 2018-03-13 |
| US10597499B2 (en) | 2020-03-24 |
| CN107250266B (zh) | 2021-10-29 |
| KR20170101254A (ko) | 2017-09-05 |
| SG11201705085UA (en) | 2017-07-28 |
| RU2017126036A3 (enExample) | 2019-05-16 |
| US20170362395A1 (en) | 2017-12-21 |
| FR3031109A1 (enExample) | 2016-07-01 |
| EP3237501A1 (en) | 2017-11-01 |
| KR102477079B1 (ko) | 2022-12-12 |
| WO2016102658A1 (en) | 2016-06-30 |
| JP7133312B2 (ja) | 2022-09-08 |
| JP2018500439A (ja) | 2018-01-11 |
| MY185543A (en) | 2021-05-19 |
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