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DE1292286B - Coating agent for the anodic coating of electrically conductive workpieces by electrophoresis - Google Patents

Coating agent for the anodic coating of electrically conductive workpieces by electrophoresis

Info

Publication number
DE1292286B
DE1292286B DEF45204A DEF0045204A DE1292286B DE 1292286 B DE1292286 B DE 1292286B DE F45204 A DEF45204 A DE F45204A DE F0045204 A DEF0045204 A DE F0045204A DE 1292286 B DE1292286 B DE 1292286B
Authority
DE
Germany
Prior art keywords
coating
electrically conductive
electrophoresis
coating agent
anodic
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
Application number
DEF45204A
Other languages
German (de)
Inventor
Tsou Ivan H
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ford Werke GmbH
Original Assignee
Ford Werke GmbH
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.)
Filing date
Publication date
Application filed by Ford Werke GmbH filed Critical Ford Werke GmbH
Publication of DE1292286B publication Critical patent/DE1292286B/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/16Amines or polyamines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/44Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
    • C09D5/448Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications characterised by the additives used
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates 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
    • C08G59/18Macromolecules 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
    • C08G59/40Macromolecules 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
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4292Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/03Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D155/00Coating compositions based on homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C09D123/00 - C09D153/00
    • C09D155/04Polyadducts obtained by the diene synthesis
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/44Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
    • C09D5/4419Coating 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
    • C09D5/4423Polyesters, esterified polyepoxides
    • C09D5/4426Esterified polyepoxides
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Molecular Biology (AREA)
  • Dispersion Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Paints Or Removers (AREA)
  • Epoxy Resins (AREA)

Description

1 ■■■·■" 2 ·■■1 ■■■ · ■ "2 · ■■

Die Erfindung bezieht sich auf ein Überzugsmittel handelsüblichen Epoxyharz mit einem mittleren für das anodische Beschichten elektrisch leitender Molekulargewicht von etwa 370 bis 450, wurden mit Werkstücke durch Elektrophorese auf der Grundlage 320 kg Leinölfettsäuren gemischt, und 1000 ecm von wäßrigen Dispersionen von Salzen carboxyl- Xylol wurden in ein Reaktionsgefäß gegeben und auf gruppenhaltiger Harze. Erfindungsgemäß enthält die 5 200° C für IV2 Stunden beheizt und alsdann auf Dispersion Salze von Polyäthylenglykol mit Mole- 230° C 4 Stunden lang beheizt, während denen kulargewicht über 200 veresterten, bei etwa über 53 ecm Wasser entnommen wurden und ein Harz 160° C hergestellten Umsetzungsprodukten einer gebildet wurde.The invention relates to a coating agent commercially available epoxy resin with a medium for anodic plating, electrically conductive molecular weights of about 370 to 450 have been used with Workpieces mixed by electrophoresis on the basis of 320 kg of linseed oil fatty acids, and 1000 ecm of aqueous dispersions of salts carboxyl-xylene were placed in a reaction vessel and on grouped resins. According to the invention, the 5 200 ° C for IV2 hours heated and then on Dispersion salts of polyethylene glycol with mol- 230 ° C heated for 4 hours during which Kular weight over 200 esterified, at about 53 ecm of water were removed and a resin 160 ° C produced reaction products one was formed.

Säurezahl von über etwa 30 aus Trimellithsäure- Stufe 2. Die Reaktionsmischung nach Stufe 1Acid number above about 30 from trimellitic acid stage 2. The reaction mixture after stage 1

anhydrid und leinölfettsäuremodifizierten Epoxyd- 10 wurde auf 160° C abgekühlt,
harzen. , Stufe 3. Dem Reaktionsprodukt der Stufe 1 wur-
anhydride and linseed oil fatty acid modified epoxy 10 was cooled to 160 ° C,
resins. , Stage 3. The reaction product of stage 1 was

Für die Herstellung'von "durch Elektrophorese . den 85kg Trimellithsäureanhydrid hinzugefügt, welaufzubringenden Lacken ist die Verwendung-von -"cties die'"Temperatur im Augenblick senkte. Die Harzen bekannt. Es handelt sich bei diesen Lack- Temperatur wurde auf 160° C zurückgebracht und Überzügen um synthetische Harzverbiridungen, die 15 so lange gehalten, bis die Reaktionsmischung klar mit Aminen und/oder Ammoniak oder schwachen wurde. "-"' For the production 'of' by electrophoresis. The 85kg of trimellitic anhydride added to which paints to be applied is the use-of - 'cties the'"lowered temperature at the moment. The resins are known. It is at this paint temperature was brought back to 160 ° C and coatings around synthetic resin compounds that held until the reaction mixture became clear with amines and / or ammonia or weak. "-"'

Alkalien neutralisiert sind. Die Harzverbindungen Stufe 4. Der klaren Reaktionsmischuiig, nachAlkalis are neutralized. The resin compounds stage 4. The clear reaction mixture after

sind löslich oder köniien mit Wasser verdünnt wer- Stufe 3 wurden 100 kg Polyäthylenglykol eines den. Als Harz wird ein Alkydharz verwendet, dessen Molekulargewichtes von 200 hinzugesetzt. Diese Bewesentlicher Bestandteil ein Additionsprodukt einer ao standteile wurden auf 160° C aufgeheizt, bis die Äthylendicarbonsäure, z.B. Maleinsäure und/oder Säurezahl von etwa 36,5 erreicht war, alsdann geseines Anhydrids ist. Die Alkydharze sind Konden- kühlt und hierauf 132 kg Methyläthylketon zusationsprodukte von Polyalkohol einerseits und Poly- gesetzt. ;..:.:; .;;;.. .-.x\:. \
carbonsäuren andererseits, wobei als Polyalkohol Stufe 5. Die Reaktionsmischung nach Stufe 4
are soluble or can be diluted with water. Stage 3 was 100 kg of polyethylene glycol. An alkyd resin with a molecular weight of 200 is used as the resin. This essential constituent, an addition product of an ao constituent, was heated to 160 ° C. until the ethylene dicarboxylic acid, for example maleic acid, and / or acid number of about 36.5 was reached, when its anhydride is then complete. The alkyd resins are condensed and 132 kg of methyl ethyl ketone addition products of polyalcohol on the one hand and poly are set on them. ; ..:.:; . ;;; .. .-. x \ :. \
carboxylic acids on the other hand, the polyalcohol being stage 5. The reaction mixture after stage 4

unter anderem Polyäthylenglykol verwendet werden 25 wurde mit 150 kg rotem Eisenoxyd auf Stufe 6 nach kann. Diese Harze können gegebenenfalls mit Fett- Hegman zerrieben, und es, wurden 85 kg. Triisosäure modifiziert sein. propanolamin hinzugefügltv" !i · -Among other things, polyethylene glycol can be used 25 with 150 kg of red iron oxide on level 6 according to can. These resins can optionally be ground with Fett-Hegman, and it was 85 kg. Triiso acid modified. propanolamine addedv " ! i · -

Bei den erfindungsgemäßen Überzugsmitteln ist Stufe 6. Alsdann wurde eine, Emulsion dutch Mi-In the case of the coating agents according to the invention, level 6 was then used.

zunächst ein leinölfettsäuremodifiziertes Harz ge- schung des Materials nach Stufe 5 mit 3800^g entbildet, das dann mit Trimellithsäureanhydrid in Re- 3° ionisiertem Wasser und Verrühren hergestellt'
aktion gebracht und schließlich mit Polyäthylenglykol :; Ein elektrisches Überzugsbad" mit einem pH-Wert „verestert ist. Letzteres, dient also zur Veresterung von. 7,0 und mit. 3,4_Gewichtsprozent Farbstoffen eines modifizierten Epoxyharzes und nicht zur BiI- wurde vorbereitet, indem die oben beschriebene dung eines Kondensationsproduktes von Polycarbon- ·· ,Emulsion mit entionisiertem Wässer verdünritwurde. säure und Polyalkohol, wie das bei dem; bekannten .35.Der elektrophoretische Niederschlag der emulgierten Alkydharz der Fall ist. Die unterschiedliche Art des Farbe wurde in einem stählernen geschliffenen Übererfindungsgemäßen Überzugsmittels bringt wesent- zugsbehälter vorgenommen, der als Kathode der liehe Vorteile mit sich. elektrischen Niederschlagszelle, diente. Stahltafeln,
First a linseed oil fatty acid-modified resin is formed from the material after stage 5 with 3800 g, which is then produced with trimellitic anhydride in re-ionized water and stirring '
action brought and finally with polyethylene glycol:; An electrical coating bath "with a pH value" is esterified. The latter, therefore, serves for the esterification of. 7.0 and with. 3.4 weight percent dyes of a modified epoxy resin and not for the formation of the above-described formation of a condensation product of Polycarbonate ··, emulsion diluted with deionized water, acid and polyalcohol, as is the case with the known .35. The electrophoretic precipitation of the emulsified alkyd resin is the case. The different type of color was brought into a steel, polished coating medium according to the invention made, which served as the cathode of the lent advantages with it. electric precipitation cell.

Die Vorteile gegenüber den bekannten Harzver- die in das Bad eingetaucht waren, wurden elektrisch bindungen bestehen nun einmal darin, daß es sich 4° geladen und dienten als Anoden der Zelle. Das Überdurch die Streukraft leichter elektrophoretisch nieder- ziehen wurde bei 37° C und einer Spannung von schlagen läßt, und das andere Mal, daß die aufge- 450 V durchgeführt. Es wurde ein gleichmäßiger brachten Überzüge ganz besonders dauerhaft sind, Niederschlag von etwa 0,025 mm Stärke erhalten, wodurch sich gute Auslaufeigenschaften ergeben. Das und die Werkstücke wurden dem Bad entnommen, modifizierte Epoxyharz gemäß der Erfindung ist im 45 Die Überzüge der Tafeln wurden anschließend wäßrigen Bad äußerst stabil und daher auch leicht 15 Minuten lang bei 200° C eingebrannt. Alsdann dispergierbar. Auf allen Flächen von metallischen wurden die Tafeln mit Salz bespritzt, und zwar geGegenständen einschließlich derjenigen mit Aus- maß dem ASTM-Testverfahren No. B 117, und sparungen oder unregelmäßig gestalteten Flächen hielten 250 Stunden aus. Andere Tafeln wurden bei lassen sich die Überzüge anbringen. Sie bilden einen 5o 250, 300 und-350 V überzogen,
hochkorrosiven Widerstand. Neben diesen Eigen- Um die Streukraft dieser Formulierung auszu-
The advantages over the known resin compounds, which were immersed in the bath, were electrical connections consist in the fact that it is charged 4 ° and served as the anodes of the cell. The lighter electrophoretically pulling down by the scattering force was carried out at 37 ° C and a voltage of 450 V, and the other time that the increased. A more evenly applied coatings are particularly durable, deposits of about 0.025 mm thick are obtained, which results in good leakage properties. That and the workpieces were removed from the bath, modified epoxy resin according to the invention is in the 45 The coatings of the panels were then extremely stable in an aqueous bath and therefore easily baked for 15 minutes at 200 ° C. Then dispersible. The panels have been sprayed with salt on all surfaces of the metal, including objects as measured by ASTM test method no. B 117, and savings or irregularly designed surfaces lasted 250 hours. Other panels were used to attach the covers. They form a 5o 250, 300 and -350 V plated,
highly corrosive resistance. In addition to these intrinsic In order to make use of the scattering power of this formulation

schaften besitzt das Überzugsmittel die, daß es das probieren, wurde ein Versuch mit drei Platten ausübliche Besandungsverfahren aushält, und die, daß geführt. Dieser Versuch erfolgte mit 370 V unter ein weiterer Überzug gleicher oder unterschiedlicher Benutzung einer Vorrichtung, die durch Zusammen-Zusammensetzung aufgebracht werden kann. Beim 55 nieten von drei rechtwinkligen .Flußeisenblechen mit Salzspritzverfahren ergeben die Überzüge einen ganz einem einzigen Niet hergestellt wurde. Jedes Blech außerordentlich hohen Test (ASTM) von 250 Stunden maß 75 · 200 mm, und die Bleche waren so zu- und mehr. sammengesetzt, daß, von der Seite gesehen, das mitt-The coating agent has properties that make it a test, a test with three plates was customary Withstands sanding processes, and the ones that led. This experiment was carried out with 370 V below Another coating of the same or different use of a device, which can be achieved by assembling it together can be applied. When riveting three right-angled Salt spray processes result in the coatings being made entirely from a single rivet. Every sheet extremely high test (ASTM) of 250 hours measured 75 x 200 mm, and the sheets were and more. composed that, seen from the side, the middle

An Hand der nachfolgenden Beispiele wird die lere Rechteck von zwei Platten verdeckt war, die Erfindung näher erläutert. 6° etwa 0,0625 mm maximal aus der vernieteten GrundThe invention is explained in more detail using the following examples, the lere rectangle was covered by two plates. 6 ° about 0.0625 mm maximum from the riveted base

linie divergierten. Der überzogene Flächenbereich der mittleren Platte ist ein Maß für die Streuung derline diverged. The covered area of the middle plate is a measure of the spread of the

Beispiel I Formulierung bei den verwendeten Bedingungen. BeiExample I Formulation under the conditions used. at

dieser Formulierung waren 75% der mittleren Platte 6g überzogen, und zwar in einer Tiefe von etwaof this formulation, 75% of the middle plate 6g was coated, to a depth of about

Eine Farbe zum elektrischen Überziehen wurde 0,025 mm innerhalb einer Minute nach der Anwenin der folgenden Weise zubereitet: dung einer Spannung, welche eine hohe StreukraftAn electric plating paint became 0.025 mm within one minute after application prepared in the following manner: generation of a voltage which has a high scattering power

Stufe 1. 800 kg eines Harzes, bestehend aus einem bedeutet.Stage 1. 800 kg of a resin consisting of one means.

Beispiel IIExample II

Es wurden wirksame Farben für elektrophoretische Überzüge wie in dem vorausgehenden Beispiel zubereitet mit der Ausnahme, daß die Polyäthylenglykole ein mittleres Molekulargewicht von 400 und 600 besaßen, an Stelle von einem Molekulargewicht von 200 für das Polyäthylenglykol des vorausgehenden Beispiels.There have been effective colors for electrophoretic Coatings prepared as in the previous example except that the polyethylene glycols possessed an average molecular weight of 400 and 600 instead of a molecular weight of 200 for the polyethylene glycol of the previous example.

Die Emulsion wurde verdünnt, so daß sie ein Überzugsbad wie in dem vorausgehenden Beispiel bildete, und wurde hierauf in gleicher Weise auf metallische Werkstücke aufgebracht.The emulsion was diluted to make a coating bath as in the previous example formed, and was then applied in the same way to metallic workpieces.

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Claims (1)

Patentanspruch:Claim: Überzugsmittel für das anodische Beschichten elektrisch leitender Werkstücke durch Elektrophorese auf der Grundlage von wäßrigen Dispersionen von Salzen carboxylgruppenhaltiger Harze, dadurch gekennzeichnet, daß sie Salze von mit Polyäthylenglykol mit Molekulargewicht über 200 veresterten, bei etwa über 160° C hergestellten Umsetzungsprodukten einer Säurezahl von über etwa 30 aus Trimellithsäureanhydrid und leinölfettsäuremodifizierten Epoxyharzen enthalten.Coating agent for the anodic coating of electrically conductive workpieces by electrophoresis based on aqueous dispersions of salts of resins containing carboxyl groups, characterized in that they contain salts of molecular weight polyethylene glycol over 200 esterified reaction products with an acid number produced at about 160 ° C of over about 30 epoxy resins modified from trimellitic anhydride and linseed oil fatty acid contain.
DEF45204A 1964-04-30 1965-02-11 Coating agent for the anodic coating of electrically conductive workpieces by electrophoresis Pending DE1292286B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US36381264A 1964-04-30 1964-04-30

Publications (1)

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DE1292286B true DE1292286B (en) 1969-04-10

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DEF45204A Pending DE1292286B (en) 1964-04-30 1965-02-11 Coating agent for the anodic coating of electrically conductive workpieces by electrophoresis
DE19651519142 Pending DE1519142A1 (en) 1964-04-30 1965-02-11 Process for the production of a coating material which is electrically deposited from an aqueous bath

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Country Status (7)

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BE (1) BE663219A (en)
DE (2) DE1292286B (en)
DK (1) DK128281B (en)
FR (1) FR1459753A (en)
GB (1) GB1100472A (en)
NL (1) NL6505500A (en)
SE (1) SE313385B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
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

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE633074A (en) * 1962-07-30
US2634245A (en) * 1950-04-27 1953-04-07 Pittsburgh Plate Glass Co Water dispersible alkyd type resins
DE1036426B (en) * 1954-11-08 1958-08-14 Bergwerksverband Gmbh Process for the production of stoving enamels
US3102868A (en) * 1960-06-17 1963-09-03 Standard Oil Co Water soluble composition for baked surface coatings comprising a polyester resin and an amino resin

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2634245A (en) * 1950-04-27 1953-04-07 Pittsburgh Plate Glass Co Water dispersible alkyd type resins
DE1036426B (en) * 1954-11-08 1958-08-14 Bergwerksverband Gmbh Process for the production of stoving enamels
US3102868A (en) * 1960-06-17 1963-09-03 Standard Oil Co Water soluble composition for baked surface coatings comprising a polyester resin and an amino resin
BE633074A (en) * 1962-07-30

Also Published As

Publication number Publication date
GB1100472A (en) 1968-01-24
DE1519142A1 (en) 1970-10-08
DK128281B (en) 1974-04-01
NL6505500A (en) 1965-11-01
SE313385B (en) 1969-08-11
BE663219A (en) 1965-08-17
FR1459753A (en) 1966-11-25

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