DE1519281A1 - Verfahren zum Beschichten von Metallen durch Elektrophorese - Google Patents
Verfahren zum Beschichten von Metallen durch ElektrophoreseInfo
- Publication number
- DE1519281A1 DE1519281A1 DE19621519281 DE1519281A DE1519281A1 DE 1519281 A1 DE1519281 A1 DE 1519281A1 DE 19621519281 DE19621519281 DE 19621519281 DE 1519281 A DE1519281 A DE 1519281A DE 1519281 A1 DE1519281 A1 DE 1519281A1
- Authority
- DE
- Germany
- Prior art keywords
- parts
- carrier
- neutralized
- acid
- product
- 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.)
- Pending
Links
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- OGVXYCDTRMDYOG-UHFFFAOYSA-N dibutyl 2-methylidenebutanedioate Chemical compound CCCCOC(=O)CC(=C)C(=O)OCCCC OGVXYCDTRMDYOG-UHFFFAOYSA-N 0.000 description 1
- VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical group [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- JHCKGVJZNIWNJK-UHFFFAOYSA-N diethyl pent-2-enedioate Chemical compound CCOC(=O)CC=CC(=O)OCC JHCKGVJZNIWNJK-UHFFFAOYSA-N 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- LDCRTTXIJACKKU-ONEGZZNKSA-N dimethyl fumarate Chemical compound COC(=O)\C=C\C(=O)OC LDCRTTXIJACKKU-ONEGZZNKSA-N 0.000 description 1
- 229960004419 dimethyl fumarate Drugs 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 235000004426 flaxseed Nutrition 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
- 230000003676 hair loss Effects 0.000 description 1
- SCFQUKBBGYTJNC-UHFFFAOYSA-N heptyl prop-2-enoate Chemical compound CCCCCCCOC(=O)C=C SCFQUKBBGYTJNC-UHFFFAOYSA-N 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- MCVVUJPXSBQTRZ-ONEGZZNKSA-N methyl (e)-but-2-enoate Chemical compound COC(=O)\C=C\C MCVVUJPXSBQTRZ-ONEGZZNKSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000019488 nut oil Nutrition 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- HPUOAJPGWQQRNT-UHFFFAOYSA-N pentoxybenzene Chemical compound CCCCCOC1=CC=CC=C1 HPUOAJPGWQQRNT-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 239000010491 poppyseed oil Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004248 saffron Substances 0.000 description 1
- 235000013974 saffron Nutrition 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- ANOBYBYXJXCGBS-UHFFFAOYSA-L stannous fluoride Chemical compound F[Sn]F ANOBYBYXJXCGBS-UHFFFAOYSA-L 0.000 description 1
- 229960002799 stannous fluoride Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4473—Mixture of polymers
-
- 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
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
-
- 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
- C08F242/00—Copolymers of drying oils with other monomers
-
- 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
-
- 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
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- 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
- C08F8/44—Preparation of metal salts or ammonium salts
-
- 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
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
- C08G63/553—Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4419—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
- C09D5/4423—Polyesters, esterified polyepoxides
-
- 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/04—Anhydrides, e.g. cyclic anhydrides
- C08F222/06—Maleic anhydride
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/901—Electrodepositable compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US222674A US3366563A (en) | 1962-09-10 | 1962-09-10 | Electropainting process and paint compositions therefor |
Publications (1)
Publication Number | Publication Date |
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DE1519281A1 true DE1519281A1 (de) | 1970-10-29 |
Family
ID=22833218
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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DE19621519281 Pending DE1519281A1 (de) | 1962-09-10 | 1962-12-29 | Verfahren zum Beschichten von Metallen durch Elektrophorese |
Country Status (8)
Country | Link |
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US (1) | US3366563A (en, 2012) |
JP (1) | JPS5222848B1 (en, 2012) |
BE (1) | BE637005A (en, 2012) |
CH (1) | CH473905A (en, 2012) |
DE (1) | DE1519281A1 (en, 2012) |
FR (1) | FR1394007A (en, 2012) |
GB (1) | GB1016957A (en, 2012) |
NL (1) | NL297540A (en, 2012) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
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US3532613A (en) * | 1963-08-14 | 1970-10-06 | Ford Motor Co | Electrocoating process |
US3674670A (en) * | 1964-12-04 | 1972-07-04 | Ppg Industries Inc | Coating method |
US3468779A (en) * | 1965-03-19 | 1969-09-23 | Celanese Coatings Co | Electrocoating process |
US3479306A (en) * | 1965-08-24 | 1969-11-18 | Dow Chemical Co | Water soluble epoxy esters |
US3428589A (en) * | 1965-09-30 | 1969-02-18 | Ashland Oil Inc | Electrocoating compositions comprising aromatic amine amidated drying oil copolymer-maleic anhydride adducts |
US3483109A (en) * | 1965-12-15 | 1969-12-09 | Ppg Industries Inc | Electrodeposition of polycarboxylic acid resin and an organophilic cation modified clay |
DE1273192B (de) * | 1966-02-05 | 1968-07-18 | Bayer Ag | Bestimmte Verbindungen als viskositaetserhoehender Zusatz zu Polyesterform- oder UEberzugsmassen |
US3532650A (en) * | 1966-03-28 | 1970-10-06 | Sherwin Williams Co | Paint vehicle prepared from homopolymers of 9-oxatetracyclo 4.4.1**2,5o**1,6o**8,10undecan 4 ol |
US3537970A (en) * | 1966-05-05 | 1970-11-03 | Gen Electric | Process for electrodepositing a polyamide acid |
US3507765A (en) * | 1966-05-05 | 1970-04-21 | Gen Electric | Method for electrocoating a polyamide acid |
US3487034A (en) * | 1966-05-16 | 1969-12-30 | Staley Mfg Co A E | Alkyd resins and their preparation from reaction mixtures comprising an alpha,alpha-dimethylol monocarboxylic acid |
US3457206A (en) * | 1966-05-16 | 1969-07-22 | Staley Mfg Co A E | Water dispersible alkyd resins comprising esterified units of an alkoxypolyoxyethylene glycol |
GB1204003A (en) * | 1966-11-07 | 1970-09-03 | Ju Kumanotani | Composition for electrophoretic deposition |
GB1206796A (en) * | 1966-11-07 | 1970-09-30 | Ju Kumanotani | Composition for electrophoretic deposition |
GB1134274A (en) * | 1966-11-29 | 1968-11-20 | British Resin Prod Ltd | Copolymer salts for water dilutable surface coating compositions |
US3533971A (en) * | 1967-02-02 | 1970-10-13 | Pan American Tung Research & D | Polymer forming composition and electrodeposition thereof |
US3445410A (en) * | 1967-05-23 | 1969-05-20 | Iowa Paint Mfg Co Inc | Storage stable coating composition comprising alkyd resin,esterified inorganic acid,and volatile buffer material |
US3518213A (en) * | 1967-08-05 | 1970-06-30 | Nippon Oil Co Ltd | Aqueous resinous coating compositions for electrophoretic deposition |
US3494882A (en) * | 1967-08-09 | 1970-02-10 | Celanese Coatings Co | Water reducible gloss enamels |
AT292151B (de) * | 1967-11-20 | 1971-08-10 | Vianova Kunstharz Ag | Wasserverdünnbares Überzugsmittel für Elektrobeschichtung |
JPS4843921B1 (en, 2012) * | 1967-12-30 | 1973-12-21 | ||
US3493482A (en) * | 1968-07-23 | 1970-02-03 | Ppg Industries Inc | Use of coal in electrodepositable compositions |
US3853803A (en) * | 1971-01-27 | 1974-12-10 | Ppg Industries Inc | Method of preparing a cationic acrylic electrodepositable interpolymer |
US3787338A (en) * | 1972-02-25 | 1974-01-22 | Gen Electric | Aqueous dispersions of finely divided lubricants in polyamide acid |
US3880793A (en) * | 1972-03-30 | 1975-04-29 | Kansai Paint Co Ltd | Emulsifiers for emulsion polymerization of vinyl monomers |
US3862067A (en) * | 1972-04-13 | 1975-01-21 | Atlantic Richfield Co | Flexible electrocoating composition derived from a low molecular weight copolymer of styrene and maleic anhydride |
US3878148A (en) * | 1972-09-28 | 1975-04-15 | Delux Australia Ltd | Film-farming compositions comprising autoxidizable material |
US3904569A (en) * | 1972-10-26 | 1975-09-09 | Continental Can Co | Metal coating compositions prepared from aqueous dispersions of carboxylic acid resin and an aliphatic polyamine |
JPS49128029A (en, 2012) * | 1973-04-09 | 1974-12-07 | ||
JPS5238573B2 (en, 2012) * | 1973-10-04 | 1977-09-29 | ||
JPS5425530B2 (en, 2012) * | 1974-03-28 | 1979-08-29 | ||
US4014830A (en) * | 1975-10-30 | 1977-03-29 | Celanese Coatings & Specialties Company | Acrylate or methacrylate modified alkyd resins and epoxy esters |
JPS5590566A (en) * | 1978-12-29 | 1980-07-09 | Kansai Paint Co Ltd | Cationic electrodeposition coating resin composition |
US4581111A (en) | 1984-03-28 | 1986-04-08 | Ppg Industries, Inc. | Treatment of ultrafiltrate by electrodialysis |
EP1873216A4 (en) * | 2005-03-22 | 2010-04-14 | Sakata Inx Corp | METHOD FOR PRODUCING AN INK COMPOSITION FOR THE OFFSET PRINT AND THE SOFTENING COMPOSITION FOR THE OFFSET PRINT THEREFOR |
US7868066B2 (en) * | 2007-07-20 | 2011-01-11 | Ppg Industries Ohio, Inc. | Aqueous dispersions and coatings comprising modified epoxy resins comprising the reaction product of rosin and a dienophile |
US8057592B2 (en) * | 2007-07-20 | 2011-11-15 | Ppg Industries Ohio, Inc. | Cationic electrodepositable coatings comprising rosin |
US8039551B2 (en) * | 2007-07-20 | 2011-10-18 | Ppg Industries Ohio, Inc. | Modified epoxy resins comprising the reaction product of rosin and a linking molecule and aqueous dispersions and coatings comprising such resins |
US7812101B2 (en) * | 2007-07-20 | 2010-10-12 | Ppg Industries Ohio, Inc. | Modified epoxy resins comprising the reaction product of a biomass derived compound and an epoxy resin, and aqueous dispersions and coatings comprising such resins |
EP2847248B1 (en) | 2012-05-08 | 2016-07-13 | DSM IP Assets B.V. | Resin, composition and use |
KR102504428B1 (ko) * | 2016-10-21 | 2023-02-27 | 바스프 에스이 | 관능성 수계 분산액의 제조 방법 |
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CA699414A (en) * | 1964-12-08 | M. Chairge Peter | Water dispersed coating compositions including neutralized drying oil-unsaturated acid anhydride adduct vehicles | |
US2414712A (en) * | 1947-01-21 | Methods of preparing modified de | ||
US2033132A (en) * | 1931-08-07 | 1936-03-10 | Ellis Foster Co | Diene type reaction product and method of making same |
US2188883A (en) * | 1936-12-22 | 1940-01-30 | Edwin T Clocker | Condensation product and method |
BE427261A (en, 2012) * | 1937-03-30 | |||
US2263923A (en) * | 1939-12-27 | 1941-11-25 | Textile Res Company | Picker check for looms |
US2386634A (en) * | 1940-03-20 | 1945-10-09 | Sprague Electric Co | Flexible electrical insulating layer |
US2820711A (en) * | 1953-06-22 | 1958-01-21 | Glidden Co | Combined stain and filler, and drying oil therefor |
BE530668A (en, 2012) * | 1953-07-27 | |||
US2941968A (en) * | 1954-11-03 | 1960-06-21 | Pittsburgh Plate Glass Co | Water dispersible interpolymers |
US2934506A (en) * | 1956-06-11 | 1960-04-26 | Devoe & Raynolds Co | Modified epoxide resins |
NL111927C (en, 2012) * | 1956-06-14 | |||
NL232342A (en, 2012) * | 1957-10-17 | |||
US3050478A (en) * | 1958-07-28 | 1962-08-21 | Glidden Co | Solidifiable fluid compositions prepared from enedioyl acids, epoxidized hydrocarbondrying oil, and conjugated dienes |
BE617996A (en, 2012) * | 1959-05-26 | |||
US3030321A (en) * | 1960-05-19 | 1962-04-17 | Cook Paint & Varnish Co | Water-soluble coating compositions |
US3200057A (en) * | 1960-12-27 | 1965-08-10 | Ford Motor Co | Electrophoretic coating process |
US3230162A (en) * | 1963-08-14 | 1966-01-18 | Ford Motor Co | Electropainting process and paint binder concentrate composition therefor |
-
0
- BE BE637005D patent/BE637005A/xx unknown
- NL NL297540D patent/NL297540A/xx unknown
-
1962
- 1962-09-10 US US222674A patent/US3366563A/en not_active Expired - Lifetime
- 1962-12-21 GB GB48306/62A patent/GB1016957A/en not_active Expired
- 1962-12-29 DE DE19621519281 patent/DE1519281A1/de active Pending
-
1963
- 1963-08-29 CH CH1065963A patent/CH473905A/de not_active IP Right Cessation
- 1963-09-02 FR FR946331A patent/FR1394007A/fr not_active Expired
- 1963-09-04 JP JP38046555A patent/JPS5222848B1/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
GB1016957A (en) | 1966-01-12 |
US3366563A (en) | 1968-01-30 |
FR1394007A (fr) | 1965-04-02 |
NL297540A (en, 2012) | 1900-01-01 |
JPS5222848B1 (en, 2012) | 1977-06-20 |
CH473905A (de) | 1969-06-15 |
BE637005A (en, 2012) | 1900-01-01 |
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