GB788806A - Compositions comprising polyepoxides and silicon-containing compounds, and cured products prepared therefrom - Google Patents
Compositions comprising polyepoxides and silicon-containing compounds, and cured products prepared therefromInfo
- Publication number
- GB788806A GB788806A GB1229255A GB1229255A GB788806A GB 788806 A GB788806 A GB 788806A GB 1229255 A GB1229255 A GB 1229255A GB 1229255 A GB1229255 A GB 1229255A GB 788806 A GB788806 A GB 788806A
- Authority
- GB
- United Kingdom
- Prior art keywords
- silicon
- polyepoxide
- compounds
- heated
- cured
- 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
- 229920000647 polyepoxide Polymers 0.000 title abstract 7
- 239000000203 mixture Substances 0.000 title abstract 6
- 239000002210 silicon-based material Substances 0.000 title 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- 239000007795 chemical reaction product Substances 0.000 abstract 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 4
- -1 cycloaliphatic Chemical group 0.000 abstract 4
- 239000000047 product Substances 0.000 abstract 4
- 239000002904 solvent Substances 0.000 abstract 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 229920001807 Urea-formaldehyde Polymers 0.000 abstract 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 229910052710 silicon Inorganic materials 0.000 abstract 3
- 239000010703 silicon Substances 0.000 abstract 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
- 239000004593 Epoxy Substances 0.000 abstract 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 2
- 229960001231 choline Drugs 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 150000002763 monocarboxylic acids Chemical class 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 150000003961 organosilicon compounds Chemical class 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229910000077 silane Inorganic materials 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- 239000008096 xylene Substances 0.000 abstract 2
- 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 abstract 1
- 229930185605 Bisphenol Natural products 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- QLTIQRMARFXIDD-UHFFFAOYSA-N [dihydroxy(methyl)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(O)O QLTIQRMARFXIDD-UHFFFAOYSA-N 0.000 abstract 1
- 239000011354 acetal resin Substances 0.000 abstract 1
- 150000001241 acetals Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 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 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 238000005266 casting Methods 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- NKKMVIVFRUYPLQ-NSCUHMNNSA-N crotononitrile Chemical compound C\C=C\C#N NKKMVIVFRUYPLQ-NSCUHMNNSA-N 0.000 abstract 1
- OLLFKUHHDPMQFR-UHFFFAOYSA-N dihydroxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](O)(O)C1=CC=CC=C1 OLLFKUHHDPMQFR-UHFFFAOYSA-N 0.000 abstract 1
- ZSZHHJYVXOIHKJ-UHFFFAOYSA-N dihydroxy-bis[2-(trifluoromethyl)phenyl]silane Chemical class FC(F)(F)C1=C(C=CC=C1)[Si](O)(O)C1=C(C=CC=C1)C(F)(F)F ZSZHHJYVXOIHKJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001033 ether group Chemical group 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229920001519 homopolymer Polymers 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 1
- NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 229920001228 polyisocyanate Polymers 0.000 abstract 1
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229920006324 polyoxymethylene Polymers 0.000 abstract 1
- 235000011118 potassium hydroxide Nutrition 0.000 abstract 1
- 238000004382 potting Methods 0.000 abstract 1
- 239000012262 resinous product Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 150000004756 silanes Chemical class 0.000 abstract 1
- 150000004819 silanols Chemical class 0.000 abstract 1
- 150000003377 silicon compounds Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- MJCYPBSRKLJZTB-UHFFFAOYSA-N trifluoroborane;dihydrate Chemical class O.O.FB(F)F MJCYPBSRKLJZTB-UHFFFAOYSA-N 0.000 abstract 1
- NLSXASIDNWDYMI-UHFFFAOYSA-N triphenylsilanol Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(O)C1=CC=CC=C1 NLSXASIDNWDYMI-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4085—Curing agents not provided for by the groups C08G59/42 - C08G59/66 silicon containing compounds
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42691054A | 1954-04-30 | 1954-04-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB788806A true GB788806A (en) | 1958-01-08 |
Family
ID=23692702
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1229255A Expired GB788806A (en) | 1954-04-30 | 1955-04-28 | Compositions comprising polyepoxides and silicon-containing compounds, and cured products prepared therefrom |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE537769A (enrdf_load_stackoverflow) |
CH (1) | CH385492A (enrdf_load_stackoverflow) |
FR (1) | FR1130032A (enrdf_load_stackoverflow) |
GB (1) | GB788806A (enrdf_load_stackoverflow) |
NL (2) | NL196867A (enrdf_load_stackoverflow) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2999836A (en) * | 1959-04-16 | 1961-09-12 | Du Pont | Reaction product of n-glycidyl-phthalimide and a dianhydride compound, process for preparing same, and modification thereof |
US3072594A (en) * | 1959-04-22 | 1963-01-08 | Walter J Saeman No Drawing | Silamine curing agents |
DE1218396B (de) * | 1960-09-01 | 1966-06-08 | Dow Corning | Verfahren zum Knitterfestmachen von Cellulosegeweben mittels Epoxyverbindungen |
US4877822A (en) * | 1985-10-07 | 1989-10-31 | Shin-Etsu Chemical Co., Ltd. | Epoxy resin composition |
US5006614A (en) * | 1988-07-05 | 1991-04-09 | Shin-Etsu Chemical Co., Ltd. | Epoxy resin composition and semiconductor device encapsulated therewith containing polymaleimide and (allyl-epoxy)novolac/siloxane graft copolymer |
US5389727A (en) * | 1988-09-09 | 1995-02-14 | Kansai Paint Company, Limited | Resin compositions and a method of curing the same |
RU2283333C2 (ru) * | 2003-08-27 | 2006-09-10 | Татьяна Валентиновна Лапицкая | Эпоксидная композиция |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU17818A1 (enrdf_load_stackoverflow) * | 1958-10-21 | 1900-01-01 | ||
BE597283A (enrdf_load_stackoverflow) * | 1959-11-21 | |||
BE790533A (fr) * | 1971-10-25 | 1973-04-25 | Ciba Geigy | Polyepoxyde-polysiloxanes durcissables |
US4038338A (en) | 1971-10-25 | 1977-07-26 | Ciba-Geigy Corporation | New polyepoxide-polysiloxane compounds |
-
0
- BE BE537769D patent/BE537769A/xx unknown
- NL NL96555D patent/NL96555C/xx active
- NL NL196867D patent/NL196867A/xx unknown
-
1955
- 1955-04-28 CH CH1910755A patent/CH385492A/de unknown
- 1955-04-28 FR FR1130032D patent/FR1130032A/fr not_active Expired
- 1955-04-28 GB GB1229255A patent/GB788806A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2999836A (en) * | 1959-04-16 | 1961-09-12 | Du Pont | Reaction product of n-glycidyl-phthalimide and a dianhydride compound, process for preparing same, and modification thereof |
US3072594A (en) * | 1959-04-22 | 1963-01-08 | Walter J Saeman No Drawing | Silamine curing agents |
DE1218396B (de) * | 1960-09-01 | 1966-06-08 | Dow Corning | Verfahren zum Knitterfestmachen von Cellulosegeweben mittels Epoxyverbindungen |
US4877822A (en) * | 1985-10-07 | 1989-10-31 | Shin-Etsu Chemical Co., Ltd. | Epoxy resin composition |
US5053445A (en) * | 1985-10-07 | 1991-10-01 | Shin-Etsu Chemical Co., Ltd. | Epoxy resin composition |
US5006614A (en) * | 1988-07-05 | 1991-04-09 | Shin-Etsu Chemical Co., Ltd. | Epoxy resin composition and semiconductor device encapsulated therewith containing polymaleimide and (allyl-epoxy)novolac/siloxane graft copolymer |
US5389727A (en) * | 1988-09-09 | 1995-02-14 | Kansai Paint Company, Limited | Resin compositions and a method of curing the same |
US5492968A (en) * | 1988-09-09 | 1996-02-20 | Kansai Paint Company Limited | Resin compositions and a method of curing the same |
RU2283333C2 (ru) * | 2003-08-27 | 2006-09-10 | Татьяна Валентиновна Лапицкая | Эпоксидная композиция |
Also Published As
Publication number | Publication date |
---|---|
BE537769A (enrdf_load_stackoverflow) | |
FR1130032A (fr) | 1957-01-30 |
NL196867A (enrdf_load_stackoverflow) | |
NL96555C (enrdf_load_stackoverflow) | |
CH385492A (de) | 1964-12-15 |
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