GB1029037A - Curable mixtures of epoxy resins and polyanhydrides or polycarboxylic acids - Google Patents
Curable mixtures of epoxy resins and polyanhydrides or polycarboxylic acidsInfo
- Publication number
 - GB1029037A GB1029037A GB8155/63A GB815563A GB1029037A GB 1029037 A GB1029037 A GB 1029037A GB 8155/63 A GB8155/63 A GB 8155/63A GB 815563 A GB815563 A GB 815563A GB 1029037 A GB1029037 A GB 1029037A
 - Authority
 - GB
 - United Kingdom
 - Prior art keywords
 - bis
 - unsaturated
 - prepared
 - compounds
 - compound
 - 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 8
 - 239000002253 acid Substances 0.000 title abstract 5
 - 229920002732 Polyanhydride Polymers 0.000 title abstract 4
 - 150000007513 acids Chemical class 0.000 title abstract 3
 - 229920000647 polyepoxide Polymers 0.000 title abstract 3
 - 239000003822 epoxy resin Substances 0.000 title 1
 - 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 title 1
 - 150000001875 compounds Chemical class 0.000 abstract 11
 - CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 4
 - 229910052799 carbon Inorganic materials 0.000 abstract 4
 - 239000003795 chemical substances by application Substances 0.000 abstract 4
 - 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
 - 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
 - OHUVHDUNQKJDKW-UHFFFAOYSA-N sodium;cyclopenta-1,3-diene Chemical compound [Na+].C=1C=C[CH-]C=1 OHUVHDUNQKJDKW-UHFFFAOYSA-N 0.000 abstract 4
 - 239000008096 xylene Substances 0.000 abstract 4
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
 - -1 Bis-(methyl)-cyclopentadienyl hydrocarbons Chemical class 0.000 abstract 3
 - FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 3
 - 239000004215 Carbon black (E152) Substances 0.000 abstract 2
 - 238000005698 Diels-Alder reaction Methods 0.000 abstract 2
 - 239000004606 Fillers/Extenders Substances 0.000 abstract 2
 - XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
 - 150000001298 alcohols Chemical class 0.000 abstract 2
 - 125000003118 aryl group Chemical group 0.000 abstract 2
 - IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 2
 - FPWYHHNBOYUKSS-UHFFFAOYSA-N di(cyclopenta-1,3-dien-1-yl)-dimethylsilane Chemical compound C=1C=CCC=1[Si](C)(C)C1=CC=CC1 FPWYHHNBOYUKSS-UHFFFAOYSA-N 0.000 abstract 2
 - 150000001991 dicarboxylic acids Chemical class 0.000 abstract 2
 - 150000002148 esters Chemical class 0.000 abstract 2
 - 239000000945 filler Substances 0.000 abstract 2
 - 125000005843 halogen group Chemical group 0.000 abstract 2
 - 229930195733 hydrocarbon Natural products 0.000 abstract 2
 - 230000003301 hydrolyzing effect Effects 0.000 abstract 2
 - 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
 - IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical compound CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 abstract 2
 - 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
 - 239000002904 solvent Substances 0.000 abstract 2
 - SYRHIZPPCHMRIT-UHFFFAOYSA-N tin(4+) Chemical compound [Sn+4] SYRHIZPPCHMRIT-UHFFFAOYSA-N 0.000 abstract 2
 - AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-Me3C6H3 Natural products CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 abstract 1
 - LBBAOPZMBSVRKG-UHFFFAOYSA-N 1,5-bis(cyclopenta-2,4-dien-1-ylmethyl)-2,4-dimethylbenzene Chemical compound C1(C=CC=C1)CC1=C(C=C(C(=C1)CC1C=CC=C1)C)C LBBAOPZMBSVRKG-UHFFFAOYSA-N 0.000 abstract 1
 - IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical compound BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 abstract 1
 - IPXDBJAYEDJFRY-UHFFFAOYSA-N 2,4-bis(cyclopenta-2,4-dien-1-ylmethyl)-1,3,5-trimethylbenzene Chemical compound C1(C=CC=C1)CC1=C(C(=C(C=C1C)C)CC1C=CC=C1)C IPXDBJAYEDJFRY-UHFFFAOYSA-N 0.000 abstract 1
 - OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical class C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 abstract 1
 - GDMNJXPBROHKAR-UHFFFAOYSA-N 5-(10-cyclopenta-2,4-dien-1-yldecyl)cyclopenta-1,3-diene Chemical compound C1(C=CC=C1)CCCCCCCCCCC1C=CC=C1 GDMNJXPBROHKAR-UHFFFAOYSA-N 0.000 abstract 1
 - AQAHYZBHLXLSHA-UHFFFAOYSA-N 5-(3-cyclopenta-2,4-dien-1-ylpropyl)cyclopenta-1,3-diene Chemical compound C1=CC=CC1CCCC1C=CC=C1 AQAHYZBHLXLSHA-UHFFFAOYSA-N 0.000 abstract 1
 - ARTSSUMMUAFQCN-UHFFFAOYSA-N 5-(4-cyclopenta-2,4-dien-1-ylcyclopent-2-en-1-yl)cyclopenta-1,3-diene Chemical compound C1C(C=CC1C1C=CC=C1)C1C=CC=C1 ARTSSUMMUAFQCN-UHFFFAOYSA-N 0.000 abstract 1
 - VBAHSPKUEILDMB-UHFFFAOYSA-N 5-(cyclopenta-2,4-dien-1-ylmethoxymethyl)cyclopenta-1,3-diene Chemical compound C1=CC=CC1COCC1C=CC=C1 VBAHSPKUEILDMB-UHFFFAOYSA-N 0.000 abstract 1
 - DXJYGHJLYRPZEJ-UHFFFAOYSA-N 5-[5-(5-cyclopenta-2,4-dien-1-ylpent-1-enoxy)pent-4-enyl]cyclopenta-1,3-diene Chemical compound C1(C=CC=C1)CCCC=COC=CCCCC1C=CC=C1 DXJYGHJLYRPZEJ-UHFFFAOYSA-N 0.000 abstract 1
 - IZSHZLKNFQAAKX-UHFFFAOYSA-N 5-cyclopenta-2,4-dien-1-ylcyclopenta-1,3-diene Chemical group C1=CC=CC1C1C=CC=C1 IZSHZLKNFQAAKX-UHFFFAOYSA-N 0.000 abstract 1
 - ZRRYUQJVPSKTQH-UHFFFAOYSA-N CC1(C=CC=C1)[Na] Chemical compound CC1(C=CC=C1)[Na] ZRRYUQJVPSKTQH-UHFFFAOYSA-N 0.000 abstract 1
 - OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
 - ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
 - 229910003910 SiCl4 Inorganic materials 0.000 abstract 1
 - 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
 - 239000000853 adhesive Substances 0.000 abstract 1
 - 230000001070 adhesive effect Effects 0.000 abstract 1
 - 125000001931 aliphatic group Chemical group 0.000 abstract 1
 - 239000004411 aluminium Substances 0.000 abstract 1
 - 229910052782 aluminium Inorganic materials 0.000 abstract 1
 - XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
 - 150000008064 anhydrides Chemical class 0.000 abstract 1
 - 125000002029 aromatic hydrocarbon group Chemical group 0.000 abstract 1
 - 230000001680 brushing effect Effects 0.000 abstract 1
 - 238000006243 chemical reaction Methods 0.000 abstract 1
 - 229920001577 copolymer Polymers 0.000 abstract 1
 - 125000006159 dianhydride group Chemical group 0.000 abstract 1
 - 150000001993 dienes Chemical class 0.000 abstract 1
 - ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 1
 - ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 abstract 1
 - 150000002170 ethers Chemical class 0.000 abstract 1
 - 238000010438 heat treatment Methods 0.000 abstract 1
 - 229910052742 iron Inorganic materials 0.000 abstract 1
 - 239000004922 lacquer Substances 0.000 abstract 1
 - 229910052751 metal Inorganic materials 0.000 abstract 1
 - 239000002184 metal Substances 0.000 abstract 1
 - 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
 - 230000003472 neutralizing effect Effects 0.000 abstract 1
 - 150000003961 organosilicon compounds Chemical class 0.000 abstract 1
 - 229920000642 polymer Polymers 0.000 abstract 1
 - 229910052700 potassium Inorganic materials 0.000 abstract 1
 - 239000011591 potassium Substances 0.000 abstract 1
 - 238000002360 preparation method Methods 0.000 abstract 1
 - 239000000047 product Substances 0.000 abstract 1
 - 239000001294 propane Substances 0.000 abstract 1
 - 239000000376 reactant Substances 0.000 abstract 1
 - 239000012262 resinous product Substances 0.000 abstract 1
 - FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 abstract 1
 - AXTNEYPUUFCBII-UHFFFAOYSA-N sodium;5-methylcyclopenta-1,3-diene Chemical compound [Na+].C[C-]1C=CC=C1 AXTNEYPUUFCBII-UHFFFAOYSA-N 0.000 abstract 1
 - 238000005507 spraying Methods 0.000 abstract 1
 - 239000010935 stainless steel Substances 0.000 abstract 1
 - 229910001220 stainless steel Inorganic materials 0.000 abstract 1
 - 150000005846 sugar alcohols Polymers 0.000 abstract 1
 - HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 1
 - 229920006305 unsaturated polyester Polymers 0.000 abstract 1
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
 - 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
 - C08G59/423—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof containing an atom other than oxygen belonging to a functional groups to C08G59/42, carbon and hydrogen
 
 - 
        
- 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
 
 - 
        
- 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
 - C08G59/4215—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
 
 - 
        
- 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)
 - Polyesters Or Polycarbonates (AREA)
 - Macromonomer-Based Addition Polymer (AREA)
 - Compositions Of Macromolecular Compounds (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| CH252262A CH427261A (de) | 1962-03-01 | 1962-03-01 | Heisshärtbares Gemisch | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| GB1029037A true GB1029037A (en) | 1966-05-11 | 
Family
ID=4235670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| GB8155/63A Expired GB1029037A (en) | 1962-03-01 | 1963-02-28 | Curable mixtures of epoxy resins and polyanhydrides or polycarboxylic acids | 
Country Status (9)
| Country | Link | 
|---|---|
| US (1) | US3271476A (en:Method) | 
| AT (1) | AT251890B (en:Method) | 
| BE (1) | BE629032A (en:Method) | 
| CH (1) | CH427261A (en:Method) | 
| DE (1) | DE1495284A1 (en:Method) | 
| DK (1) | DK103322C (en:Method) | 
| ES (1) | ES285600A1 (en:Method) | 
| GB (1) | GB1029037A (en:Method) | 
| NL (2) | NL135324C (en:Method) | 
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US3391223A (en) * | 1967-01-03 | 1968-07-02 | American Cyanamid Co | Polyesterification reaction products of a polyhydric alcohol and a 3, 4-dicarboxy-1, , 3, 4-tetrahydro-1-naphthalenesuccinic dianhydride | 
| US4034014A (en) * | 1970-10-16 | 1977-07-05 | Allied Chemical Corporation | Production of polyanhydride epoxide prepolymer compositions | 
| US3957727A (en) * | 1973-12-18 | 1976-05-18 | Canadian Patents And Development Limited | Epoxy composition containing acid anhydride compound obtained from nadic methyl anhydride | 
| DE3109900A1 (de) * | 1981-03-14 | 1982-09-23 | Hoechst Ag, 6000 Frankfurt | Mit wasser verduennbares epoxyd, verfahren zu seiner herstellung und dessen verwendung | 
| JPH0660294B2 (ja) * | 1986-06-05 | 1994-08-10 | ソマ−ル株式会社 | エポキシ樹脂系粉体塗料組成物 | 
| US5948922A (en) * | 1997-02-20 | 1999-09-07 | Cornell Research Foundation, Inc. | Compounds with substituted cyclic hydrocarbon moieties linked by secondary or tertiary oxycarbonyl containing moiety providing reworkable cured thermosets | 
| CN107868116B (zh) * | 2016-09-26 | 2021-02-26 | 华东师范大学 | 一类六环系甾体衍生物及其合成方法 | 
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US2667501A (en) * | 1953-02-10 | 1954-01-26 | Gen Electric | Cyclopentadienylsilanes | 
| GB812675A (en) * | 1956-10-24 | 1959-04-29 | Huels Chemische Werke Ag | Process for the preparation of unsaturated polyester copolymers | 
| US2912442A (en) * | 1956-11-23 | 1959-11-10 | Du Pont | 2, 3, 6, 7 naphthalenetetracarboxylic acid and its functional derivatives | 
| BE566688A (en:Method) * | 1957-04-12 | |||
| NL245996A (en:Method) * | 1958-12-02 | 
- 
        0
        
- BE BE629032D patent/BE629032A/xx unknown
 - NL NL289600D patent/NL289600A/xx unknown
 - NL NL135324D patent/NL135324C/xx active
 
 - 
        1962
        
- 1962-03-01 CH CH252262A patent/CH427261A/de unknown
 
 - 
        1963
        
- 1963-02-26 DK DK88063AA patent/DK103322C/da active
 - 1963-02-28 GB GB8155/63A patent/GB1029037A/en not_active Expired
 - 1963-02-28 DE DE19631495284 patent/DE1495284A1/de active Pending
 - 1963-02-28 ES ES285600A patent/ES285600A1/es not_active Expired
 - 1963-02-28 AT AT159363A patent/AT251890B/de active
 - 1963-02-28 US US261890A patent/US3271476A/en not_active Expired - Lifetime
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| CH427261A (de) | 1966-12-31 | 
| BE629032A (en:Method) | |
| AT251890B (de) | 1967-01-25 | 
| NL135324C (en:Method) | |
| DE1495284A1 (de) | 1969-04-10 | 
| DK103322C (da) | 1965-12-13 | 
| ES285600A1 (es) | 1963-08-01 | 
| NL289600A (en:Method) | |
| US3271476A (en) | 1966-09-06 | 
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