NO116730B - - Google Patents
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- Publication number
 - NO116730B NO116730B NO15922665A NO15922665A NO116730B NO 116730 B NO116730 B NO 116730B NO 15922665 A NO15922665 A NO 15922665A NO 15922665 A NO15922665 A NO 15922665A NO 116730 B NO116730 B NO 116730B
 - Authority
 - NO
 - Norway
 - Prior art keywords
 - fatty acid
 - groups
 - acid esters
 - hydroxy
 - carboxyl groups
 - Prior art date
 
Links
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 35
 - 239000000194 fatty acid Substances 0.000 claims abstract description 35
 - 229930195729 fatty acid Natural products 0.000 claims abstract description 35
 - 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 29
 - -1 fatty acid ester Chemical class 0.000 claims abstract description 26
 - 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 15
 - 150000008064 anhydrides Chemical class 0.000 claims abstract description 11
 - 125000003700 epoxy group Chemical group 0.000 claims abstract description 6
 - 229920000728 polyester Polymers 0.000 claims abstract description 5
 - 150000001491 aromatic compounds Chemical class 0.000 claims abstract description 4
 - IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
 - 229910052757 nitrogen Inorganic materials 0.000 claims description 6
 - 238000004519 manufacturing process Methods 0.000 claims description 4
 - 238000000034 method Methods 0.000 claims description 4
 - 239000004033 plastic Substances 0.000 claims description 4
 - 229920003023 plastic Polymers 0.000 claims description 4
 - OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 20
 - 239000002253 acid Substances 0.000 abstract description 18
 - 239000011230 binding agent Substances 0.000 abstract description 16
 - QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 10
 - 150000004665 fatty acids Chemical class 0.000 abstract description 10
 - HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 9
 - 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 description 9
 - POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 abstract description 7
 - 239000000203 mixture Substances 0.000 abstract description 7
 - 235000020354 squash Nutrition 0.000 abstract description 7
 - ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract description 6
 - 239000007864 aqueous solution Substances 0.000 abstract description 6
 - 229910021529 ammonia Inorganic materials 0.000 abstract description 5
 - 239000003822 epoxy resin Substances 0.000 abstract description 5
 - 229920000647 polyepoxide Polymers 0.000 abstract description 5
 - YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract description 4
 - LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract description 4
 - AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract description 4
 - 229920001577 copolymer Polymers 0.000 abstract description 4
 - 235000021388 linseed oil Nutrition 0.000 abstract description 4
 - 239000000944 linseed oil Substances 0.000 abstract description 4
 - GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract description 3
 - JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 abstract description 2
 - BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract description 2
 - ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 2
 - 150000007513 acids Chemical class 0.000 abstract description 2
 - 239000013543 active substance Substances 0.000 abstract description 2
 - 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 abstract description 2
 - 230000003472 neutralizing effect Effects 0.000 abstract description 2
 - 150000002989 phenols Chemical class 0.000 abstract description 2
 - 229940086542 triethylamine Drugs 0.000 abstract description 2
 - 229920005989 resin Polymers 0.000 abstract 2
 - 239000011347 resin Substances 0.000 abstract 2
 - 150000001735 carboxylic acids Chemical class 0.000 abstract 1
 - 235000019864 coconut oil Nutrition 0.000 abstract 1
 - 239000003240 coconut oil Substances 0.000 abstract 1
 - 229940113083 morpholine Drugs 0.000 abstract 1
 - 235000011044 succinic acid Nutrition 0.000 abstract 1
 - 150000003444 succinic acids Chemical class 0.000 abstract 1
 - 229960004418 trolamine Drugs 0.000 abstract 1
 - 150000005846 sugar alcohols Polymers 0.000 description 8
 - PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
 - XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 6
 - 125000003118 aryl group Chemical group 0.000 description 6
 - 238000001035 drying Methods 0.000 description 6
 - 150000002148 esters Chemical group 0.000 description 6
 - LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 5
 - JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 5
 - 239000003921 oil Substances 0.000 description 5
 - 235000019198 oils Nutrition 0.000 description 5
 - 239000000047 product Substances 0.000 description 5
 - 239000000243 solution Substances 0.000 description 5
 - 230000015572 biosynthetic process Effects 0.000 description 4
 - 150000003839 salts Chemical group 0.000 description 4
 - OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
 - KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
 - 239000007795 chemical reaction product Substances 0.000 description 3
 - 238000000576 coating method Methods 0.000 description 3
 - 239000002274 desiccant Substances 0.000 description 3
 - 239000011521 glass Substances 0.000 description 3
 - FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
 - 238000006386 neutralization reaction Methods 0.000 description 3
 - 239000000049 pigment Substances 0.000 description 3
 - 238000003756 stirring Methods 0.000 description 3
 - 239000002966 varnish Substances 0.000 description 3
 - UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
 - 239000000853 adhesive Substances 0.000 description 2
 - 230000001070 adhesive effect Effects 0.000 description 2
 - 150000001412 amines Chemical class 0.000 description 2
 - 239000011248 coating agent Substances 0.000 description 2
 - 229960002887 deanol Drugs 0.000 description 2
 - 239000012972 dimethylethanolamine Substances 0.000 description 2
 - 239000006185 dispersion Substances 0.000 description 2
 - 239000003995 emulsifying agent Substances 0.000 description 2
 - 125000004185 ester group Chemical group 0.000 description 2
 - 238000010438 heat treatment Methods 0.000 description 2
 - 239000003960 organic solvent Substances 0.000 description 2
 - 239000003973 paint Substances 0.000 description 2
 - 235000013162 Cocos nucifera Nutrition 0.000 description 1
 - 244000060011 Cocos nucifera Species 0.000 description 1
 - 239000004593 Epoxy Substances 0.000 description 1
 - 244000068988 Glycine max Species 0.000 description 1
 - 235000010469 Glycine max Nutrition 0.000 description 1
 - 239000004640 Melamine resin Substances 0.000 description 1
 - 229920000877 Melamine resin Polymers 0.000 description 1
 - 239000004721 Polyphenylene oxide Substances 0.000 description 1
 - 239000002174 Styrene-butadiene Substances 0.000 description 1
 - MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
 - 150000008065 acid anhydrides Chemical class 0.000 description 1
 - 230000001680 brushing effect Effects 0.000 description 1
 - MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
 - 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
 - 239000004359 castor oil Substances 0.000 description 1
 - 235000019438 castor oil Nutrition 0.000 description 1
 - 238000006243 chemical reaction Methods 0.000 description 1
 - 239000003795 chemical substances by application Substances 0.000 description 1
 - 239000013078 crystal Substances 0.000 description 1
 - 230000003247 decreasing effect Effects 0.000 description 1
 - 230000001627 detrimental effect Effects 0.000 description 1
 - 239000000428 dust Substances 0.000 description 1
 - 230000001804 emulsifying effect Effects 0.000 description 1
 - 239000000839 emulsion Substances 0.000 description 1
 - 230000032050 esterification Effects 0.000 description 1
 - 238000005886 esterification reaction Methods 0.000 description 1
 - 150000002170 ethers Chemical class 0.000 description 1
 - 238000002474 experimental method Methods 0.000 description 1
 - 239000000945 filler Substances 0.000 description 1
 - 239000005002 finish coating Substances 0.000 description 1
 - 239000003292 glue Substances 0.000 description 1
 - ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
 - 239000011874 heated mixture Substances 0.000 description 1
 - 238000005470 impregnation Methods 0.000 description 1
 - 239000000976 ink Substances 0.000 description 1
 - 239000004922 lacquer Substances 0.000 description 1
 - 239000007788 liquid Substances 0.000 description 1
 - 125000005609 naphthenate group Chemical group 0.000 description 1
 - 230000007935 neutral effect Effects 0.000 description 1
 - 239000012299 nitrogen atmosphere Substances 0.000 description 1
 - 231100000252 nontoxic Toxicity 0.000 description 1
 - 230000003000 nontoxic effect Effects 0.000 description 1
 - 230000003647 oxidation Effects 0.000 description 1
 - 238000007254 oxidation reaction Methods 0.000 description 1
 - 229920000570 polyether Polymers 0.000 description 1
 - 238000006116 polymerization reaction Methods 0.000 description 1
 - 229920002689 polyvinyl acetate Polymers 0.000 description 1
 - 239000011118 polyvinyl acetate Substances 0.000 description 1
 - 238000001556 precipitation Methods 0.000 description 1
 - 238000002360 preparation method Methods 0.000 description 1
 - 239000002987 primer (paints) Substances 0.000 description 1
 - 239000011541 reaction mixture Substances 0.000 description 1
 - 239000002904 solvent Substances 0.000 description 1
 - 238000005507 spraying Methods 0.000 description 1
 - 239000011115 styrene butadiene Substances 0.000 description 1
 - 229920003048 styrene butadiene rubber Polymers 0.000 description 1
 
Classifications
- 
        
- 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
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
 - C08F8/00—Chemical modification by after-treatment
 - C08F8/14—Esterification
 
 - 
        
- 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
 - C08G59/4292—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids
 
 - 
        
- 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
 - C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
 - C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
 - C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
 - C08G63/40—Polyesters derived from ester-forming derivatives of polycarboxylic acids or of polyhydroxy compounds, other than from esters thereof
 - C08G63/42—Cyclic ethers; Cyclic carbonates; Cyclic sulfites; Cyclic orthoesters
 
 - 
        
- 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
 - C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
 - C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
 - C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
 - C08G63/46—Polyesters chemically modified by esterification
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
 - C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
 - C08L67/08—Polyesters modified with higher fatty oils or their acids, or with resins or resin acids
 
 - 
        
- 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
 - C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
 - C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
 - C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
 - C08F2810/00—Chemical modification of a polymer
 - C08F2810/30—Chemical modification of a polymer leading to the formation or introduction of aliphatic or alicyclic unsaturated groups
 
 - 
        
- 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)
 - Organic Chemistry (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Health & Medical Sciences (AREA)
 - Medicinal Chemistry (AREA)
 - Polymers & Plastics (AREA)
 - Oil, Petroleum & Natural Gas (AREA)
 - Life Sciences & Earth Sciences (AREA)
 - Engineering & Computer Science (AREA)
 - Materials Engineering (AREA)
 - Wood Science & Technology (AREA)
 - General Chemical & Material Sciences (AREA)
 - Epoxy Resins (AREA)
 - Polyesters Or Polycarbonates (AREA)
 - Paints Or Removers (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| NL6409137A NL6409137A (instruction) | 1964-08-07 | 1964-08-07 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| NO116730B true NO116730B (instruction) | 1969-05-12 | 
Family
ID=19790745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| NO15922665A NO116730B (instruction) | 1964-08-07 | 1965-08-05 | 
Country Status (10)
| Country | Link | 
|---|---|
| AT (1) | AT279902B (instruction) | 
| BE (1) | BE667945A (instruction) | 
| CH (1) | CH458740A (instruction) | 
| DE (1) | DE1570461C3 (instruction) | 
| DK (1) | DK115013B (instruction) | 
| FR (1) | FR1442890A (instruction) | 
| GB (1) | GB1090669A (instruction) | 
| NL (2) | NL6409137A (instruction) | 
| NO (1) | NO116730B (instruction) | 
| SE (1) | SE326040B (instruction) | 
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US3624013A (en) * | 1967-02-10 | 1971-11-30 | Desoto Inc | Heat-hardenable water-dispersible resins derived from polyhydric polyethers and mixtures thereof with benzoguanamine-formaldehyde condensates particularly adapted for electrodeposition | 
| EP0009526A1 (en) * | 1978-10-10 | 1980-04-16 | Mobil Oil Corporation | Water-solubilizable epoxy resin and coating composition comprising the resin for metal food contact surfaces | 
| US4357456A (en) * | 1981-08-28 | 1982-11-02 | Shell Oil Company | Low viscosity vinyl ester resins | 
| GB2353999B (en) * | 1999-09-07 | 2003-04-30 | Chinese Petroleum Corp | Curable system of self-emulsified aqueous epoxy resin and its polymeric hybrids | 
- 
        0
        
- NL NL126763D patent/NL126763C/xx active
 
 - 
        1964
        
- 1964-08-07 NL NL6409137A patent/NL6409137A/xx unknown
 
 - 
        1965
        
- 1965-08-05 BE BE667945D patent/BE667945A/xx unknown
 - 1965-08-05 DE DE1965D0047908 patent/DE1570461C3/de not_active Expired
 - 1965-08-05 CH CH1100265A patent/CH458740A/de unknown
 - 1965-08-05 DK DK402665A patent/DK115013B/da unknown
 - 1965-08-05 AT AT725465A patent/AT279902B/de not_active IP Right Cessation
 - 1965-08-05 NO NO15922665A patent/NO116730B/no unknown
 - 1965-08-05 GB GB3357165A patent/GB1090669A/en not_active Expired
 - 1965-08-05 SE SE1026565A patent/SE326040B/xx unknown
 - 1965-08-05 FR FR27428A patent/FR1442890A/fr not_active Expired
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| FR1442890A (fr) | 1966-06-17 | 
| DE1570461C3 (de) | 1978-10-26 | 
| DE1570461B2 (de) | 1975-02-27 | 
| BE667945A (instruction) | 1966-02-07 | 
| DK115013B (da) | 1969-08-25 | 
| AT279902B (de) | 1970-03-25 | 
| CH458740A (de) | 1968-06-30 | 
| NL6409137A (instruction) | 1966-02-08 | 
| SE326040B (instruction) | 1970-07-13 | 
| GB1090669A (en) | 1967-11-15 | 
| NL126763C (instruction) | |
| DE1570461A1 (de) | 1970-02-26 | 
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