GB959028A - Epoxide resin compositions - Google Patents
Epoxide resin compositionsInfo
- Publication number
- GB959028A GB959028A GB375760A GB375760A GB959028A GB 959028 A GB959028 A GB 959028A GB 375760 A GB375760 A GB 375760A GB 375760 A GB375760 A GB 375760A GB 959028 A GB959028 A GB 959028A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- hydroxy
- nitro
- phenol
- aralkyl
- 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
- 239000000203 mixture Substances 0.000 title abstract 2
- 229920000647 polyepoxide Polymers 0.000 title abstract 2
- 239000003822 epoxy resin Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 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 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 4
- -1 nitro, hydroxy Chemical group 0.000 abstract 4
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 abstract 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 4
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 abstract 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 3
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 abstract 2
- 229940013085 2-diethylaminoethanol Drugs 0.000 abstract 2
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 abstract 2
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 2
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 abstract 2
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- AHDSRXYHVZECER-UHFFFAOYSA-N 2,4,6-tris[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(CN(C)C)=C(O)C(CN(C)C)=C1 AHDSRXYHVZECER-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- 150000008065 acid anhydrides Chemical class 0.000 abstract 1
- 239000000908 ammonium hydroxide Substances 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- XABJJJZIQNZSIM-UHFFFAOYSA-N azane;phenol Chemical class [NH4+].[O-]C1=CC=CC=C1 XABJJJZIQNZSIM-UHFFFAOYSA-N 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000002924 oxiranes Chemical group 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 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
- 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
- C08G59/68—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 catalysts used
- C08G59/686—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 catalysts used containing nitrogen
-
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL260711D NL260711A (cs) | 1960-02-02 | ||
NL127810D NL127810C (cs) | 1960-02-02 | ||
BE599759D BE599759A (cs) | 1960-02-02 | ||
GB375760A GB959028A (en) | 1960-02-02 | 1960-02-02 | Epoxide resin compositions |
CH29061A CH396410A (de) | 1960-02-02 | 1961-01-10 | Härtbares Gemisch aus Epoxydverbindungen und Polycarbonsäureanhydriden |
FR850902A FR1282310A (fr) | 1960-02-02 | 1961-01-27 | Mélanges durcissables à base de résines époxydes et d'anhydrides d'acides polycarboxyliques |
DE19611445284 DE1445284B2 (de) | 1960-02-02 | 1961-02-01 | Verwendung von quaternaeren substituierten ammoniumsalzen von phenolen als beschleuniger beim haerten von epoxydverbindungen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB375760A GB959028A (en) | 1960-02-02 | 1960-02-02 | Epoxide resin compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB959028A true GB959028A (en) | 1964-05-27 |
Family
ID=9764386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB375760A Expired GB959028A (en) | 1960-02-02 | 1960-02-02 | Epoxide resin compositions |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE599759A (cs) |
CH (1) | CH396410A (cs) |
DE (1) | DE1445284B2 (cs) |
GB (1) | GB959028A (cs) |
NL (2) | NL260711A (cs) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3151540A1 (de) * | 1980-12-29 | 1982-08-19 | Ciba-Geigy GmbH, 7867 Wehr | "verwendung von transparenten anhydridhaertbaren epoxidgiessharzen" |
EP0102916A3 (de) * | 1982-05-13 | 1984-09-05 | Siemens Aktiengesellschaft | Isolierband zur Herstellung einer mit einer heisshärtenden Epoxidharz-Säureanhydrid-Mischung imprägnierten Isolierhülse für elektrische Leiter |
EP0240459A1 (de) * | 1986-03-26 | 1987-10-07 | Ciba-Geigy Ag | Härtbare Stoffgemische |
-
0
- NL NL127810D patent/NL127810C/xx active
- BE BE599759D patent/BE599759A/xx unknown
- NL NL260711D patent/NL260711A/xx unknown
-
1960
- 1960-02-02 GB GB375760A patent/GB959028A/en not_active Expired
-
1961
- 1961-01-10 CH CH29061A patent/CH396410A/de unknown
- 1961-02-01 DE DE19611445284 patent/DE1445284B2/de not_active Ceased
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3151540A1 (de) * | 1980-12-29 | 1982-08-19 | Ciba-Geigy GmbH, 7867 Wehr | "verwendung von transparenten anhydridhaertbaren epoxidgiessharzen" |
EP0102916A3 (de) * | 1982-05-13 | 1984-09-05 | Siemens Aktiengesellschaft | Isolierband zur Herstellung einer mit einer heisshärtenden Epoxidharz-Säureanhydrid-Mischung imprägnierten Isolierhülse für elektrische Leiter |
EP0240459A1 (de) * | 1986-03-26 | 1987-10-07 | Ciba-Geigy Ag | Härtbare Stoffgemische |
Also Published As
Publication number | Publication date |
---|---|
DE1445284B2 (de) | 1973-04-19 |
CH396410A (de) | 1965-07-31 |
BE599759A (cs) | |
NL260711A (cs) | |
NL127810C (cs) | |
DE1445284A1 (de) | 1968-12-12 |
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