CH615451A5 - Curable preparation based on epoxy resins and use thereof for producing coatings on metallic and non-metallic surfaces. - Google Patents

Curable preparation based on epoxy resins and use thereof for producing coatings on metallic and non-metallic surfaces. Download PDF

Info

Publication number: CH615451A5
Authority: CH; Switzerland
Prior art keywords: weight; preparation; epoxy resin; metallic; preparation according
Prior art date: 1975-03-28

Application number

CH383876A

Other languages

German (de)

English (en)

Inventor

Rainer Dr Schinabeck

Original Assignee

American Velodur Metal

Priority date (The priority date 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 date listed.)

1975-03-28

Filing date

1976-03-26

Publication date

1980-01-31

1975-03-28 Priority claimed from US05/562,969 external-priority patent/US3976613A/en

1975-05-20 Priority claimed from US05/579,203 external-priority patent/US3992358A/en

1976-03-26 Application filed by American Velodur Metal filed Critical American Velodur Metal

1980-01-31 Publication of CH615451A5 publication Critical patent/CH615451A5/de

Links

238000002360 preparation method Methods 0.000 title claims abstract description 66
229920000647 polyepoxide Polymers 0.000 title claims abstract description 34
239000003822 epoxy resin Substances 0.000 title claims abstract description 32
238000000576 coating method Methods 0.000 title claims abstract description 26
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 claims description 11
239000004848 polyfunctional curative Substances 0.000 claims abstract description 18
239000000945 filler Substances 0.000 claims abstract description 17
239000004593 Epoxy Substances 0.000 claims abstract description 16
239000002904 solvent Substances 0.000 claims abstract description 16
239000007788 liquid Substances 0.000 claims abstract description 9
239000002270 dispersing agent Substances 0.000 claims abstract description 8
238000010438 heat treatment Methods 0.000 claims abstract description 8
239000000446 fuel Substances 0.000 claims abstract description 5
239000004850 liquid epoxy resins (LERs) Substances 0.000 claims abstract description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 22
239000011248 coating agent Substances 0.000 claims description 17
239000000463 material Substances 0.000 claims description 10
239000000203 mixture Substances 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 9
239000000377 silicon dioxide Substances 0.000 claims description 7
229910000831 Steel Inorganic materials 0.000 claims description 6
125000003700 epoxy group Chemical group 0.000 claims description 6
239000003921 oil Substances 0.000 claims description 6
150000002894 organic compounds Chemical class 0.000 claims description 6
239000000843 powder Substances 0.000 claims description 6
229920002545 silicone oil Polymers 0.000 claims description 6
239000010959 steel Substances 0.000 claims description 6
229910021485 fumed silica Inorganic materials 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
230000015572 biosynthetic process Effects 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 3
239000002245 particle Substances 0.000 claims description 3
229910001220 stainless steel Inorganic materials 0.000 claims description 3
239000010935 stainless steel Substances 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 2
150000007513 acids Chemical class 0.000 claims description 2
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
150000001491 aromatic compounds Chemical class 0.000 claims description 2
239000002828 fuel tank Substances 0.000 claims description 2
230000009931 harmful effect Effects 0.000 claims description 2
150000002391 heterocyclic compounds Chemical class 0.000 claims description 2
239000003350 kerosene Substances 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
239000000758 substrate Substances 0.000 claims description 2
239000000126 substance Substances 0.000 abstract description 5
239000003502 gasoline Substances 0.000 abstract description 2
230000001464 adherent effect Effects 0.000 abstract 1
238000004062 sedimentation Methods 0.000 abstract 1
229920000570 polyether Polymers 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
150000002989 phenols Chemical class 0.000 description 5
239000001294 propane Substances 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
239000004721 Polyphenylene oxide Substances 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 3
-1 4-hydroxy-2-methylphenyl Chemical group 0.000 description 3
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
239000000470 constituent Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
239000000047 product Substances 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
239000003513 alkali Substances 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 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 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
238000005259 measurement Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
229920003986 novolac Polymers 0.000 description 2
KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 2
229960001553 phloroglucinol Drugs 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
239000004575 stone Substances 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 1
ZPANWZBSGMDWON-UHFFFAOYSA-N 1-[(2-hydroxynaphthalen-1-yl)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CC3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 ZPANWZBSGMDWON-UHFFFAOYSA-N 0.000 description 1
RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 1
WZCQOMUGRAWORP-UHFFFAOYSA-N 4-[4-(4-hydroxyphenyl)cyclohexyl]phenol Chemical compound C1=CC(O)=CC=C1C1CCC(C=2C=CC(O)=CC=2)CC1 WZCQOMUGRAWORP-UHFFFAOYSA-N 0.000 description 1
229910052580 B4C Inorganic materials 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
229910000906 Bronze Inorganic materials 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000530268 Lycaena heteronea Species 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
229940106691 bisphenol a Drugs 0.000 description 1
238000009835 boiling Methods 0.000 description 1
INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
239000010951 brass Substances 0.000 description 1
239000010974 bronze Substances 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
239000001273 butane Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
238000005266 casting Methods 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000004568 cement Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
238000005536 corrosion prevention Methods 0.000 description 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
150000002118 epoxides Chemical group 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000010439 graphite Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001282 iso-butane Substances 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
238000000034 method Methods 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000000178 monomer Substances 0.000 description 1
PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229940079877 pyrogallol Drugs 0.000 description 1
239000010453 quartz Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000004576 sand Substances 0.000 description 1
HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
229910010271 silicon carbide Inorganic materials 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000002023 wood Substances 0.000 description 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
- C08G59/62—Alcohols or phenols
- C08G59/621—Phenols
- C08G59/623—Aminophenols

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Epoxy Resins (AREA)

CH383876A 1975-03-28 1976-03-26 Curable preparation based on epoxy resins and use thereof for producing coatings on metallic and non-metallic surfaces. CH615451A5 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US05/562,969 US3976613A (en)	1975-03-28	1975-03-28	Composition and process for treating and repairing metallic and non-metallic surfaces
US05/579,203 US3992358A (en)	1975-04-10	1975-05-20	Epoxy resin compositions

Publications (1)

Publication Number	Publication Date
CH615451A5 true CH615451A5 (en)	1980-01-31

Family

ID=27073136

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH383876A CH615451A5 (en)	1975-03-28	1976-03-26	Curable preparation based on epoxy resins and use thereof for producing coatings on metallic and non-metallic surfaces.

Country Status (5)

Country	Link
AT (1)	AT372095B (ro)
CH (1)	CH615451A5 (ro)
MX (1)	MX147887A (ro)
NL (1)	NL7602955A (ro)
RO (1)	RO70251A (ro)

1976
- 1976-03-17 AT AT195076A patent/AT372095B/de not_active IP Right Cessation
- 1976-03-22 NL NL7602955A patent/NL7602955A/xx not_active Application Discontinuation
- 1976-03-26 MX MX16405576A patent/MX147887A/es unknown
- 1976-03-26 RO RO7685317A patent/RO70251A/ro unknown
- 1976-03-26 CH CH383876A patent/CH615451A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
AT372095B (de)	1983-08-25
MX147887A (es)	1983-01-31
NL7602955A (nl)	1976-09-30
RO70251A (ro)	1982-05-10
ATA195076A (de)	1983-01-15

Legal Events

Date	Code	Title	Description
1984-11-30	PL	Patent ceased
1985-02-28	AEN	Scope or validity of the patent modified	Free format text: DAS PATENT IST AM 841207 GESTUETZT AUF DAS AM 841116 EINGEREICHTE WIEDEREINSETZUNGSGESUCH, AUFGRUND VON ART. 47 PATG WIEDER IN KRAFT GESETZT WORDEN
1985-03-29	PUE	Assignment	Owner name: SIGAL TRADING SOCIETE ANONYME
1996-04-15	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
US2765288A (en)	1956-10-02	Coating compositions containing coal tar pitch and an epoxy ether resin
US3356624A (en)	1967-12-05	Epoxy resin based traffic paint compositions
DE4206392A1 (de)	1993-09-02	Haertungsmittel fuer epoxidharze
US3355511A (en)	1967-11-28	Flame retardant epoxy compositions containing polyglycidyl ethers of hexahalo bicycloheptadiene bisphenols
US2528417A (en)	1950-10-31	Epoxy ether compositions containing phenolic pitch
EP0200674A1 (de)	1986-11-05	(Acylthiopropyl)-Polyphenole
DE1595484C3 (de)	1974-11-07	Verfahren zur Herstellung von Ricinusölpolyglycidyläthem und deren Verwendung zur Herstellung einer härtbaren Masse
US3062771A (en)	1962-11-06	Compositions of epoxy resin and aromatic hydrocarbon oils
DE2549656A1 (de)	1976-05-13	Neue haertungsmittel fuer epoxidharze
US5759691A (en)	1998-06-02	Phosphorus-modified coating compositions, a process for their preparation, and their use
EP0794206B1 (de)	2002-06-12	Phosphormodifizierte Überzugsmassen, ein Verfahren zu ihrer Herstellung und ihre Verwendung als Intumeszenzbeschichtung
US2910455A (en)	1959-10-27	Glycidyl polyethers from an epihalohydrin and a bis(4-hydroxy-3 allyl phenyl) alkane
DE2612211C2 (ro)	1990-09-06
US3294742A (en)	1966-12-27	Halogen-containing thermosetting epoxy resin
DE2025159B2 (de)	1977-03-31	Verfahren zum herstellen von formkoerpern und ueberzuegen
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DE1570366A1 (de)	1969-09-04	Haertbare Mischungen aus Epoxydharzen und ditertiaeren Aminen