GB819107A - Coating compositions containing coal products and polyepoxides - Google Patents
Coating compositions containing coal products and polyepoxidesInfo
- Publication number
- GB819107A GB819107A GB2396357A GB2396357A GB819107A GB 819107 A GB819107 A GB 819107A GB 2396357 A GB2396357 A GB 2396357A GB 2396357 A GB2396357 A GB 2396357A GB 819107 A GB819107 A GB 819107A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- epoxy
- coal tar
- added
- xylene
- 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 5
- 239000003245 coal Substances 0.000 title 1
- 239000008199 coating composition Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 9
- 239000004593 Epoxy Substances 0.000 abstract 6
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 abstract 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 4
- 239000011280 coal tar Substances 0.000 abstract 4
- -1 epoxide compounds Chemical class 0.000 abstract 4
- 239000008096 xylene Substances 0.000 abstract 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- 239000004744 fabric Substances 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 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 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000011294 coal tar pitch Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 abstract 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 abstract 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 2
- 125000003700 epoxy group Chemical group 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000011521 glass Substances 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 150000002989 phenols Chemical class 0.000 abstract 2
- 239000000049 pigment Substances 0.000 abstract 2
- 229920000570 polyether Polymers 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- AVGQTJUPLKNPQP-UHFFFAOYSA-N 1,1,1-trichloropropane Chemical compound CCC(Cl)(Cl)Cl AVGQTJUPLKNPQP-UHFFFAOYSA-N 0.000 abstract 1
- ODGBRFFGIINVHG-UHFFFAOYSA-N 1-[2-(cyclohexen-1-yl)propan-2-yl]cyclohexene Chemical compound C=1CCCCC=1C(C)(C)C1=CCCCC1 ODGBRFFGIINVHG-UHFFFAOYSA-N 0.000 abstract 1
- 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
- ATTHUQCSFAMCJI-UHFFFAOYSA-N 2-(cyclohexene-1-carbonyloxy)ethyl cyclohexene-1-carboxylate Chemical compound C=1CCCCC=1C(=O)OCCOC(=O)C1=CCCCC1 ATTHUQCSFAMCJI-UHFFFAOYSA-N 0.000 abstract 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical class CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 abstract 1
- DDNLLYYWFSTMHR-UHFFFAOYSA-N 2-[2-[2-chloro-4-[2-(oxiran-2-yl)ethoxy]cyclohexyl]oxyethyl]oxirane Chemical compound ClC1CC(OCCC2OC2)CCC1OCCC1CO1 DDNLLYYWFSTMHR-UHFFFAOYSA-N 0.000 abstract 1
- FADZHHSLTCASRS-UHFFFAOYSA-N 2-[3-[3-chloro-5-[3-(oxiran-2-yl)propoxy]phenoxy]propyl]oxirane Chemical compound C=1C(OCCCC2OC2)=CC(Cl)=CC=1OCCCC1CO1 FADZHHSLTCASRS-UHFFFAOYSA-N 0.000 abstract 1
- FSYPIGPPWAJCJG-UHFFFAOYSA-N 2-[[4-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane Chemical compound C1OC1COC(C=C1)=CC=C1OCC1CO1 FSYPIGPPWAJCJG-UHFFFAOYSA-N 0.000 abstract 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 abstract 1
- KGYYLUNYOCBBME-UHFFFAOYSA-M 4-fluoro-2-phenyl-4-(4-propylcyclohexyl)cyclohexa-1,5-diene-1-carboxylate Chemical compound C1CC(CCC)CCC1C1(F)C=CC(C([O-])=O)=C(C=2C=CC=CC=2)C1 KGYYLUNYOCBBME-UHFFFAOYSA-M 0.000 abstract 1
- 241000272525 Anas platyrhynchos Species 0.000 abstract 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 229910000831 Steel Inorganic materials 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000008360 acrylonitriles Chemical class 0.000 abstract 1
- 238000007792 addition Methods 0.000 abstract 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- DALDUXIBIKGWTK-UHFFFAOYSA-N benzene;toluene Chemical compound C1=CC=CC=C1.CC1=CC=CC=C1 DALDUXIBIKGWTK-UHFFFAOYSA-N 0.000 abstract 1
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- YVWBQGFBSVLPIK-UHFFFAOYSA-N cyclohex-2-ene-1-carboxylic acid Chemical compound OC(=O)C1CCCC=C1 YVWBQGFBSVLPIK-UHFFFAOYSA-N 0.000 abstract 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 abstract 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 229920001971 elastomer Polymers 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000002657 fibrous material Substances 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 229920003986 novolac Polymers 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 150000007519 polyprotic acids Polymers 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 239000010453 quartz Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 239000005060 rubber Substances 0.000 abstract 1
- 239000004576 sand Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 239000010959 steel Substances 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- 150000003626 triacylglycerols Chemical class 0.000 abstract 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 239000005050 vinyl trichlorosilane Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L95/00—Compositions of bituminous materials, e.g. asphalt, tar, pitch
-
- 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Structural Engineering (AREA)
- Civil Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paints Or Removers (AREA)
Abstract
Compositions suitable for the production of laminates or coatings consists of a coal tar, refined coal tar, or coal tar pitch having a softening point below 90 DEG C. and a solubility in carbon disulphide of at least 50 per cent in admixture with a polyepoxide containing more than one epoxy group per molecule. For the production of non-skid coatings siliceous material, e.g. sand may be added up to 50 per cent by weight of the mixture or alternately glass cloth or fibres may be added to produce laminates. Types of epoxide compounds used are (1) epoxy monomers, e.g. epoxidized triglycerides; 1,4 - bis - (2,3 - epoxypropoxy) - benzene; 4,4-bis-(2,3-epoxypropoxy)-diphenyl ether; 1,8 - bis - (2,3 - epoxypropoxy) - cyclo - hexane; 1,3 - bis - (4,5 - epoxypentoxy) - 5 - chlorobenzene; 1,4 - bis - (3,4 - epoxybutoxy)-2-chlorocyclohexane; (2) and (4) epoxy polyethers of phenols or alcohols obtained by reacting epichlorhydrin in alkaline medium with polyhydric phenols or alcohols; (3) glycidyl ethers of novolac resins; (5) epoxy esters of polybasic acids, e.g. diglycidylphthalate or adipate; (6) polymers or copolymers of epoxy-containing monomers possessing at least one ethylenic linkage, e.g. allyl glycidyl ether; (7) polyepoxides having one or more internal epoxy groups, e.g. vinyl cyclohexene dioxide, epoxidized 2,2 - bis - (cyclohexenyl) - propane and epoxidized unsaturated esters, e.g. epoxidized tetrahydrobenzoate, dicrotyl phthalate and ethylene glycol dicyclohexenecarboxylate. The polyepoxide may be present in amounts of 15-75 per cent by weight of the mixture. When the components are both liquid the composition may be prepared by simple admixture or the components may be liquefied by heating; alternatively they may be dissolved in solvents, e.g. isopropyl or butyl alcohols, acetone, methyl ethyl or methyl butyl ketones esters, e.g. ethyl acetate, butyl acetate, cellosolve acetate; ether alcohols, e.g. ethers of glycols; chlorinated hydrocarbons, e.g. trichloropropane, chloroform. aromatic hydrocarbons, e.g. toluene benzene, xylene. Solvents which remain in the cured composition may also be used, e.g. diethyl phthalate, dibutyl phthalate liquid epoxy compounds, e.g. glycidyl phenyl ether; acetonitrile. Solid or semi-solid polyepoxides may be used with the liquid epoxy compounds. Pigments, dyes, fillers, stabilizers may be added or resins, e.g. alkyd resins, vinyls or rubbers. Curing agents comprise polycarboxylic acids or anhydrides; amines and adducts of amines and epoxides; urea-melamine- or phenol-formaldehyde resins dicyandiamide. In preparing non-skid surfaces for ashphalt runways, roads, warehouse floors, pavements, tennis courts, ship decks; the additions of small inert particles of silicious materials are desirable. Laminates are made by impregnating sheets of fibrous materials with the compositions. The sheets may be made of glass cloth, cotton wool, leather or synthetic fibres, e.g. acrylonitriles, polyesters, polyurethanes. polyvinyls, paper duck muslin cloth previously sized with chrome methacrylate or vinyl trichlorosilane. Moulded products may also be obtained. In examples: (1) a refined coal tar having a softening point of 25 DEG C. sp. gr. 1.25 and 86.5 per cent soluble in carbon disulphide was mixed with a polyether obtained by reacting epichlorhydrin and 2,2 - bis - (4 - hydroxyphenyl) - propane pigment consisting of Asbestibe 3X and Carbosil was added with xylene to give the required viscosity diethylamine triamine as added as curing agents and the mixture applied to steel panels and air-dried; (5) the compositions consisted of refined coal tar, vinylcyclohexene dioxide, xylene and benzyldimethylamine; (8) a non-skid surfacing composition was prepared from a polyglydicyl phenyl ether, coal tar pitch, xylene diethylamine triamine and crushed quartz.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60072056A | 1956-07-30 | 1956-07-30 | |
| US60520556A | 1956-07-30 | 1956-07-30 | |
| US605206A US3033088A (en) | 1956-08-20 | 1956-08-20 | Composition comprising a coal product, a polyepoxide and abrasive particles and process for treating surfaces therewith |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB819107A true GB819107A (en) | 1959-08-26 |
Family
ID=27416813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2396357A Expired GB819107A (en) | 1956-07-30 | 1957-07-29 | Coating compositions containing coal products and polyepoxides |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE559629A (en) |
| CH (1) | CH368624A (en) |
| DE (1) | DE1162963C2 (en) |
| FR (1) | FR1188506A (en) |
| GB (1) | GB819107A (en) |
| NL (1) | NL101001C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2660319A1 (en) * | 1990-03-27 | 1991-10-04 | Intevep Sa | CORROSION - RESISTANT COATING BASED ON OIL COKE AND EPOXY RESIN AND PROCESS FOR PREPARING THE SAME. |
| CN107083070A (en) * | 2017-04-28 | 2017-08-22 | 华北水利水电大学 | Composite epoxy asphalt ground surface material and preparation method thereof |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1165791B (en) * | 1964-03-19 | Gelsenkirchener Bergwerks Ag | Corrosion protection agent with thixotropic properties | |
| NL237472A (en) * | 1958-03-27 | |||
| DE1184311B (en) * | 1962-03-24 | 1964-12-31 | Bergwerksverband Gmbh | Process for elastic and / or plastic consolidation of coals and secondary rocks |
| NL292892A (en) * | 1962-05-17 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2060715A (en) * | 1933-01-13 | 1936-11-10 | Du Pont | Synthetic resins |
| US2599817A (en) * | 1948-01-12 | 1952-06-10 | Shell Dev | Carbo-polymerization homopolymers of unsaturated alcohol ethers of glycidols and their homologs |
| US2506486A (en) * | 1948-04-21 | 1950-05-02 | Union Carbide & Carbon Corp | Thermosetting resin from a diphenol and a diglycidyl ether of a diphenol |
| US2528417A (en) * | 1949-01-25 | 1950-10-31 | Shell Dev | Epoxy ether compositions containing phenolic pitch |
-
1957
- 1957-07-29 BE BE559629A patent/BE559629A/xx unknown
- 1957-07-29 GB GB2396357A patent/GB819107A/en not_active Expired
- 1957-07-29 FR FR1188506D patent/FR1188506A/en not_active Expired
- 1957-07-29 DE DE1957N0013951 patent/DE1162963C2/en not_active Expired
- 1957-07-29 CH CH4893657A patent/CH368624A/en unknown
- 1957-07-29 NL NL219412A patent/NL101001C/xx active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2660319A1 (en) * | 1990-03-27 | 1991-10-04 | Intevep Sa | CORROSION - RESISTANT COATING BASED ON OIL COKE AND EPOXY RESIN AND PROCESS FOR PREPARING THE SAME. |
| CN107083070A (en) * | 2017-04-28 | 2017-08-22 | 华北水利水电大学 | Composite epoxy asphalt ground surface material and preparation method thereof |
| CN107083070B (en) * | 2017-04-28 | 2019-05-31 | 华北水利水电大学 | Composite epoxy asphalt ground surface material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| BE559629A (en) | 1958-01-29 |
| DE1162963B (en) | 1964-02-13 |
| NL101001C (en) | 1962-04-16 |
| FR1188506A (en) | 1959-09-23 |
| DE1162963C2 (en) | 1975-08-14 |
| CH368624A (en) | 1963-04-15 |
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