WO1986001526A1 - Aqueous electrophoretic coating by cathodic deposition and method for coating an electric conductor substrate - Google Patents

Aqueous electrophoretic coating by cathodic deposition and method for coating an electric conductor substrate Download PDF

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Publication number
WO1986001526A1
WO1986001526A1 PCT/DE1985/000261 DE8500261W WO8601526A1 WO 1986001526 A1 WO1986001526 A1 WO 1986001526A1 DE 8500261 W DE8500261 W DE 8500261W WO 8601526 A1 WO8601526 A1 WO 8601526A1
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WO
WIPO (PCT)
Prior art keywords
mixture
crosslinking
parts
agents
polyisocyanates
Prior art date
Application number
PCT/DE1985/000261
Other languages
German (de)
English (en)
French (fr)
Inventor
Michael Geist
Georg SCHÖN
Arnold Dobbelstein
Günther OTT
Original Assignee
Basf Lacke + Farben Ag
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 Basf Lacke + Farben Ag filed Critical Basf Lacke + Farben Ag
Priority to DE8585903983T priority Critical patent/DE3567902D1/de
Priority to BR8507240A priority patent/BR8507240A/pt
Priority to AT85903983T priority patent/ATE40397T1/de
Publication of WO1986001526A1 publication Critical patent/WO1986001526A1/de

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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
    • C09D5/4488—Cathodic paints
    • C09D5/4496—Cathodic paints characterised by the nature of the curing agents
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
    • C08G18/0809—Manufacture of polymers containing ionic or ionogenic groups containing cationic or cationogenic groups
    • C08G18/0814—Manufacture of polymers containing ionic or ionogenic groups containing cationic or cationogenic groups containing ammonium groups or groups forming them
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
    • C08G18/6415—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63 having nitrogen
    • C08G18/643—Reaction products of epoxy resins with at least equivalent amounts of amines
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen

Definitions

  • Aqueous electrodeposition coating composition which can be deposited by cathode and method for coating an electrically conductive substrate
  • the invention relates to a cathodically depositable aqueous electrodeposition coating composition which comprises a synthetic resin binder which contains amino and / or hydroxyl groups and can be made water-soluble by protonation with acids, and a mixture of crosslinking agents and pigments, fillers and corrosion ⁇ protection inhibitors, paint auxiliaries, optionally catalysts and in an amount up to 15% by weight, based on the total weight of the coating composition, contains organic solvents.
  • the coating compositions contain crosslinking or hardening agents.
  • Blocked polyisocyanates can be used as preferred crosslinking agents. These only react with the reactive amino or hydroxyl groups when the coated article has been heated to a higher temperature which is sufficient to remove the blocking of the isocyanate. Mixtures of different polyisocyanates are also used.
  • EP-B 4 090 likewise describes a cathodically depositable aqueous electrodeposition coating composition which consists of a synthetic resin binder with amino groups, which can be made water-soluble by adding acid, and a crosslinking agent containing ester groups, which in the basic medium at temperatures above 140 C react with the primary and / or secondary amino groups of the synthetic resin binder to form amides.
  • small amounts of other modifying resins such as blocked isocyanates, may also be emulsified in.
  • deposited films with an acceptable surface can be produced. Nevertheless, there is an urgent desire to significantly improve these surfaces in order to possibly enable a two-layer structure in the overall coating.
  • the cause of the film surface defects is often that the surface roughness of the sheet to be coated is caused by the burned-in film. by becoming visible on its surface. This also results in a topcoat with a disturbed surface. The surface roughness is therefore shown upwards.
  • the invention is therefore based on the object of avoiding the formation of background defects in the baked film and of providing an electrocoating material which leads to a better surface quality.
  • an electrocoating material which contains an externally crosslinking synthetic resin binder and a mixture of differently reactive crosslinking agents.
  • the present invention thus relates to an electrocoating material of the type mentioned at the outset, which is characterized in that the mixture of the crosslinking agents contains at least two differently reactive crosslinking agents based on activated esters and / or polyisocyanates blocked with different blocking agents , where differently reactive means that the
  • Crosslinking reaction when heated at temperatures which are o at least 10 ° C apart and where the first reacting crosslinker is present in a proportion of 15 to 60 mol%, based on the crosslinking agent mixture.
  • DSC Different scanning calorimetry
  • Another method familiar to the paint specialist is to mix the various crosslinking agents with a standard binder and to prepare a paint therefrom.
  • This varnish is used to make films and bake them at different temperatures.
  • the baked films are now rubbed off with solvent.
  • This test determines the stoving temperature at which the films are exposed by the solvent, e.g. 20 double strokes can no longer be attacked with a cotton ball soaked in solvent. This makes it very easy to rank different networkers.
  • the test binder which is advantageously chosen is the binder which is also to later contain the crosslinker mixture.
  • epoxy resins in various designs are particularly suitable, as described, inter alia, in the patents DE-PS 27 01 002, EP-B 4 090, DE-PS 31 08 073 and the patent application EP-A 12 463 are described. There and also at other points, other groups of binders are also mentioned which are suitable for the use according to the invention. Because of the particularly good protection against corrosion, however, epoxy resins are currently preferred.
  • Cationic water-dispersible synthetic resins are known as binders for electrocoating paints.
  • DE-OS 27 01 002 describes such a resin, which is a reaction product of a polyepoxide, a secondary amine and an organic polyol with at least 2 alcoholic primary hydroxyl groups.
  • the resins are formed by chain extension of high molecular weight polyepoxides with at least 2 epoxy groups per molecule. The chain extension is achieved by an organic polyol and the water dispersibility by addition of a secondary amine.
  • DE-OS 31 08 073 describes a binder for electrocoating, the application of which results in greater layer thicknesses.
  • the binders used are reaction products of
  • C) optionally up to 60% by weight, based on the total binder, polyfunctional alcohols, carboxylic acids and / or SH compounds with a molecular weight of 500 to 5000 and
  • polyepoxides Materials which contain two or more epoxy groups in the molecule can be used as polyepoxides (component A). Compounds with two epoxy groups in the molecule are preferred.
  • the polyepoxides have a relatively low molecular weight of at most 750, preferably 400-500.
  • the polyepoxides can, for example, be polyglycidyl ethers of polyphenols, such as bisphenols, advantageously e.g. Bisphenol A. These polyepoxides can be prepared by etherifying a polyphenol with an epihalohydrin in the presence of alkali.
  • Suitable phenolic compounds are bis (4-hydroxyphenyl) 2,2-propane, 4,4 * -dihydroxybenzophenone, bis (4-hydroxyphenyl) -1, 1-ethane, bis (4-hydroxyphenyl) -1, 1 -isobutane, bis (4-hydroxy-tertiary-butylphenyl) -2,2-propane, bis (2-hydroxynaphthyl methane, 1,5-dihydroxynaphthalene and hydantoin epoxides.
  • polyepoxides are polyglycidyl ethers of phenolic novolak resins.
  • Polyglycidyl esters of aromatic polycarboxylic acids can also advantageously be used.
  • component B aliphatic and / or alicyclic see polyfunctional alcohols or carboxylic acids with a molecular weight below 350 used.
  • Diols such as ethylene glycol, diglycol, dipropylene glycol, dibutylene glycol, triglycol, 1,2-propanediol, 1,3-propanediol, 2,2-dimethyl-1,3-propanediol, 2,2-diethyl-1,3-pro pandiol, 2-methyl-2-ethyl-l, 3-propanediol, 2-methyl-2-propyl-l, 3-propanediol, 2-ethyl-2-butyl-l, 3-propanediol, 1,2-butanediol , 1,4-butanediol, 2,3-butanediol, 2-ethyl-1,4-butanediol, 2,2-diethyl-l, 3-butanediol, butene-2-diol-1,4, 1,2-pendanediol , 1,5-pentanediol, 3-
  • Some preferred diols are 2,2-dimethyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 2,2-dimethyl-3-hydroxypropyl-2,2-dimethylhydroxy-propionate and 4,4 * -Isopropylidene biscyclohexanol.
  • dicarboxylic acids are suitable as carboxylic acids, such as oxalic acid, malonic acid, 2,2-dimethylmalonic acid, succinic acid, glutaric acid, adipic acid, hexahydrophthalic acid, maleic acid, fumaric acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, itaconic acid, citraconic acid , Mesaconic acid and glutaconic acid.
  • Preferred dicarboxylic acids are e.g. 2,2-dimethylmalonic acid and hexahydrophthalic acid.
  • Polyfunctional alcohols, carboxylic acids and SH compounds are suitable as component C.
  • the diols, triols and higher polymeric polyols such as polyester polyols and polyether polyols.
  • Polyester polyols, and among them the polycaprolactone polyols are particularly preferred.
  • the polyester polyols can be prepared by polyesterification of organic polycarboxylic acids or their anhydrides with organic polyols which contain primary hydroxyl groups.
  • the polycarboxylic acids and the polyols are usually aliphatic or aromatic dicarboxylic acids and diols.
  • the diols used to make the polyesters include alkylene glycols such as ethylene glycol, butylene glycol, neopentyl glycol and other glycols such as cyclohexane dimethanol.
  • the acid component of the polyester consists primarily of low molecular weight carboxylic acids or their anhydrides with 2 to 18 carbon atoms in the molecule.
  • Suitable acids are, for example, phthalic acid, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, glutaric acid, hexachlorheptanedicarboxylic acid and tetrachlorophthalic acid.
  • their anhydrides can also be used, insofar as they exist / are used.
  • Suitable polyester polyols are those which are derived from lactones.
  • the amine used for the reaction with the epoxy compound as component D can be primary, secondary or tertiary, secondary amines being particularly suitable.
  • the amine should preferably be water-soluble. Examples of such amines are mono- and dialkylamines, such as methylamine, ethylamine, propylamine, butylamine, dimethylamine, diethylamine, dipropylamine, methylbutylamine and the same.
  • Polyamines with primary and secondary amino groups can be reacted with the epoxide groups in the form of their ketimines. The reaction of the amine with the epoxy groups often already occurs when the starting substances are mixed. If necessary, heating to 50 to 150 ° C. is necessary.
  • At least such an amount of amine must be used that the resin assumes a cationic character, that is to say that it moves to the cathode under the influence of a voltage in the coating bath if it is soluble by adding an acid has been made.
  • Acids suitable for neutralizing the amines include boric acid, lactic acid, formic acid, acetic acid, propionic acid, butyric acid and hydrochloric acid. The modification with amino groups therefore has the purpose of making the binder water-soluble and cationic.
  • ketins Modification with ketins has also proven particularly useful in the binder of the electrocoat coating composition according to the invention.
  • ketimines are the reaction product of primary amines with ketones. In this way, in addition to other methods not described in more detail here, free primary amino groups can be realized in the resin after the resin has dispersed in the water.
  • the epoxy resins also contain free hydroxyl groups, which are introduced by a specific synthetic route.
  • hydroxyl groups and frequently also amino groups are available in the customary and also market-relevant binders for crosslinking with an admixed external crosslinker.
  • These and other known cationic binders can be used in the present invention.
  • a crosslinking agent is added to the electrocoat material, which effects the crosslinking of the binder at elevated temperatures.
  • the crosslinkers suitable for the crosslinking agent mixture according to the invention must therefore be reactive towards hydroxyl and amino groups.
  • Suitable crosslinking components for the electrodeposition coating composition according to the invention are e.g. blocked polyisocyanates as described in detail in DE-AS 20 57 799 and DE-OS 31 08 073.
  • the blocked polyisocyanates are stable at room temperature and are only unblocked at elevated temperature.
  • the polyisocyanates released can then react both with the hydroxyl groups formed by opening the epoxy rings to form urethane and with the free amino groups of the binder with urea formation during the stoving process.
  • Crosslinking agents or mixtures of crosslinking agents generally make up about 5 to 60% by weight of the binder. 20 to about 40% by weight of the binder are preferred.
  • Any polyisocyanates in which the isocyanate groups have been reacted with a compound can be used in the invention, so that the blocked polyisocyanate formed is resistant to hydroxyl groups at room temperature, at elevated temperature, generally from about 90 to about 300 C, but reacts
  • Any organic polyisocyanates suitable for crosslinking can be used in the production of the blocked polyisocyanates.
  • the isocyanates which contain about 3 to about 36, in particular about 8 to about 15, carbon atoms are preferred.
  • suitable diisocyanates are trimethylene diisocyanate, tetramethylene diisocyanate ,.
  • Polyisocyanates of higher isocyanate functionality are used, examples of which are tris (4-isocyanatophenyl) methane, 1,3,5-triisocyanatobenzene, 2,4,6-triisocyanatotoluene, 1,3,5-tris (6-isocyanatohexyl) biuret, bis (2,5-diisocyanato-4-methylphenyl) methane and polymeric polyisocyanates such as dimers and trimers of diisocyanatotoluene.
  • Any suitable aliphatic, cycloaliphatic or aromatic alkyl monoalcohols can be used to block the polyisocyanates.
  • suitable aliphatic, cycloaliphatic or aromatic alkyl monoalcohols can be used to block the polyisocyanates.
  • aliphatic alcohols such as methyl, ethyl, chloroethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, 3,3,5-trimethylhexyl, decyl and lauryl alcohol
  • cycloaliphatic alcohols such as cyclopentanol and cyclohexanol
  • aromatic alkyl alcohols such as phenylcarbinol and methylphenylcarbinol.
  • the blocked polyisocyanates are prepared by reacting a sufficient amount of an alcohol with the organic polyisocyanate so that no free isocyanate groups are present.
  • the reaction between the organic polyisocyanate and the blocking agent is exothermic. Therefore, the polyisocyanate and the blocking agent are preferably mixed at a temperature which is not higher than 80 ° C., in particular lower than 50 ° C.
  • the chemistry of the blocked isocyanates is based on the reversible equilibrium reaction of urethane formation at higher temperatures.
  • the NCO groups can be blocked and regenerated by heating if necessary.
  • the blocked isocyanates unlike the free isocyanates, do not react at room temperature, the mixtures prepared with hydroxyl-containing polyesters or polyethers are stable in storage.
  • One-component polyurethane lacquers of this type are "stoving systems" which only crosslink at higher temperatures with the blocking agent being split off. The tendency towards thermal dissociation of the blocked isocyanates depends both on the isocyanate component and on the chemical structure of the blocking agent.
  • the thermally most stable are urethanes from aliphatic isocyanates and primary alcohols, which only split up at about 230 ° C.
  • the urethanes of the aromatic isocyanates with primary alcohols are less stable.
  • the phenyl urethanes of the aromatic isocyanates are the easiest to split.
  • the temperature range in which the cleavage to the isocyanate occurs can be determined by heating the dissolved cleaver with a solution of acetyl cellulose.
  • aliphatic amines can be used as blocking agents for polyisocyanates.
  • cleavage temperatures of blocked polyisocyanates depend in each case on the blocking agent and on the type of isocyanate, it is possible to obtain differently reactive crosslinking agents in the electrodeposition coating composition according to the invention by using different blocking agents for a particular isocyanate.
  • Either different alcohols, different amines or, at the same time, alcohols and amines are used as blocking agents for polyisocyanates in the electrodeposition coating composition according to the invention.
  • crosslinkers includes the group of crosslinkers which bring about crosslinking by transesterification or amidation.
  • the reactive ester group can be activated both in the acid and in the alcohol part.
  • Examples of this are the transesterification crosslinkers described in EP-A 12 463, which are activated in the alcohol part by a ⁇ -hydroxy group.
  • DE-OS 31 03 642 describes the crosslinking by aminolysis of crosslinking agents containing / - -hyrdoxyalkyl ester groups.
  • the crosslinking is carried out by means of alkoxy esters, ester groups, amino groups and by means of ⁇ T and ⁇ £ - activating groups described.
  • the crosslinking agent mixture of the electrodeposition coating composition according to the invention can also consist simultaneously of blocked polyisocyanates and crosslinking agents with activated ester groups.
  • EP-B 4 090 describes a crosslinking agent mixture which, in addition to activated ester components, also to a small extent from other crosslinking agents, such as blocked isocyanates. It was found that small additions of other crosslinkers to activated esters do not lead to an improvement in the surface quality of the baked films. In view of the statement in EP-B 4 090 that the admixed crosslinkers should only be used to a small extent, it was not obvious to mix differently reactive crosslinkers in the claimed molar ratios, since an improvement in the surface quality was not predictable.
  • the crosslinkers react in a graduated manner due to their different reactivity, ie. H. at different times and at different stoving temperatures.
  • the temperatures at which the crosslinking reaction of the differently reactive crosslinkers begins are at least 10 ° C. apart.
  • the first reacting crosslinker fixes a good flow before the overall film could shrink over the roughness of the metallic substrate.
  • the crosslinking agent which then becomes effective serves for the final crosslinking of the pre-fixed, gel-like coating film. If only one crosslinker component is used, the shrinking process occurs during the baking in such a way that the roughness of the metallic substrate is imaged upwards.
  • the invention also relates to a method for coating an electrically conductive substrate, in which the substrate is immersed in an aqueous bath based on a synthetic resin binder containing at least partially neutralized with acids, cationic amino and / or hydroxyl groups
  • a reactor equipped with a heater, a cooler, a stirrer, a thermometer, an outlet line leading to a washing device and a device for introducing
  • reaction mixture is kept at 50 ° C. for 75 minutes, then the condenser is turned off and 3.6 parts of dibutyltin dilaurate are added.
  • the heating device is switched on and the reaction _ ,. mixture is heated to 65.6 ° over the course of 45 minutes. In the course of two hours and 50 minutes, 3,184 parts of 1,1,1-trimethylolpropane are added, the temperature rising from 65.6 to 120 ° C. The reaction mixture is held at this temperature for 90 minutes, then 10 560 0 parts of 2-ethoxyethanol are added.
  • the resulting product is a solution of a polyurethane crosslinking agent.
  • the minimum baking temperature of this polyurethane crosslinking agent is 165 ° C. 5 b) Representation of crosslinker II
  • Desmodur N trimerized hexamethylene diisocyanate, 75% strength in ethylglycol acetate-xylene
  • 1,290 parts of dibutylamine are then added dropwise over a period of 6 hours.
  • the temperature is kept below 45 ° C.
  • the mixture is then cooled to room temperature and the crosslinker solution is filtered.
  • the minimum baking temperature of this polyurethane crosslinker is 140 C.
  • the binder is prepared analogously to ⁇ Example A of EP-A 70 550.
  • a suitable reactor 1,019 parts of a commercially available Epoxy resin based on bisphenol A (epoxy equivalent weight 485), 39 parts of xylene and 265 parts of a polycaprolactone polyol (available under the trade name PCP 0200 from Union Carbide Corp.).
  • PCP 0200 commercially available Epoxy resin based on bisphenol A
  • PCP 0200 polycaprolactone polyol
  • 1,024 parts of a commercially available epoxy resin based on bisphenol A (epoxy equivalent weight 188), 142 parts of neopentyl glycol and 40 parts of xylene are placed in a suitable reactor and heated to 125.degree. 4.1 parts of dimethylbenzylamine are added and the temperature is allowed to rise to 130.degree. This temperature is maintained / until an epoxy equivalent weight of 425 is reached and 366 parts of a polycaprolactone polyol (available under the trade name PCP 0200 from Union Carbide Corp.) and 3.1 parts of dimethylbenzylamine are added. The temperature is kept at 130 ° C. until the epoxy equivalent weight has reached 1085.
  • 1,800 parts of this product are introduced with 2,447 parts of deionized water and mixed with 2,460 parts of titanium dioxide, 590 parts of an extender based on aluminum silicate, 135 parts of lead silicate and 37 parts of carbon black. This mixture is reduced to a Hegman fineness of 5 to 7 in a grinding unit. Then 1,255 parts of deionized water are added in order to achieve the desired paste consistency. This gray paste is very stable in storage.
  • electrocoat materials are Coatings made.
  • 2,000 parts by weight of the binder dispersions are mixed with 775 parts by weight of the gray pigment paste.
  • the bath solid is adjusted to 20% (150 ° C., 30 ') with deionized water.
  • the bath is then left to age for 3 days with stirring.
  • the coating films are deposited on zinc-phosphated sheet for 2 minutes.
  • the voltage is chosen so that typical layer thicknesses are achieved for the individual binders.
  • the bath temperature is 27 C.
  • the deposited films are baked at 180 ° C for 20 minutes.
  • 802 parts of the polyurethane crosslinker I are added to the binder I. After the addition and incorporation of hexylglycol, 201 parts of crosslinker II and 12 parts of lead octoate are added and mixed in for 15 minutes. 2350 parts of the batch are dispersed in another reactor with 3,015 parts of deionized water, 24.7 parts of glacial acetic acid and 48.3 parts of an emulsifier solution.
  • binder III 1 854 parts of the binder III are mixed with 452 parts of the crosslinking agent II and 194 parts of the crosslinking agent III and with 60 parts of lead octoate and then dispersed in 3 220 parts of deionized water and 35 parts of glacial acetic acid.
  • Binder I is mixed with 1 003 parts of polyurethane crosslinker I.
  • the reaction mixture is thereby cooled to 110 ° C., and 64 parts of methylethanolamine and 40 parts of a 70% strength solution of methylisobutyldiketimine of diethylene triamine are added.
  • the diketimine is obtained from 1 mole of diethylene triamine and 2 moles of methyl isobutyl ketone.
  • the manufacture is described in US Pat. No. 3,523,925.
  • the reaction mixture is now kept at 115 ° C. for 1 hour.
  • the mixture is then diluted with 104 parts of hexylglycol and the reaction mixture is kept at 115 ° C. for a further hour.
  • 2,350 parts of the batch are mixed in another reactor with 3,015 parts of deionized water, 24.7 parts of glacial acetic acid and 840.3 parts of an emulsifier solution dispersed.
  • 1,189 parts of the crosslinking agent j are mixed to give the binder II described above. As a result, the temperature drops. 107 parts of the above-mentioned ketimine and 80 parts of methylethanolamine are added. This causes the temperature to rise again. It is kept at 115 ° C. for one hour and 76 parts of phenoxypropanol and 38 parts are added
  • binder III 1 854 parts of the binder III are mixed with 646 parts of the crosslinking agent II and 60 parts of lead octoate and then in 3 220 parts of deionized water and
  • the primed sheets were coated with 50 ⁇ m of an acrylate topcoat.
  • the DOI value is determined in a relative measurement and is a measure of the gloss behavior of an almost ideally reflective surface.
  • the measured value at the reflection maximum that is to say the angle of incidence of a light beam is equal to the angle of reflection, is related to the measured value which is obtained when the angles differ by 0.3 °.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
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  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Polyurethanes Or Polyureas (AREA)
PCT/DE1985/000261 1984-09-01 1985-08-02 Aqueous electrophoretic coating by cathodic deposition and method for coating an electric conductor substrate WO1986001526A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DE8585903983T DE3567902D1 (en) 1984-09-01 1985-08-02 Aqueous electrophoretic coating by cathodic deposition and method for coating an electric conductor substrate
BR8507240A BR8507240A (pt) 1984-09-01 1985-08-02 Composicao de revestimento de laca de eletroimersao aquosa,catodicamente precipitavel e processo para o revestimento de um substrato eletricamente condutor
AT85903983T ATE40397T1 (de) 1984-09-01 1985-08-02 Kathodisch abscheidbares waessriges elektrotauchlackueberzugsmittel und verfahren zum beschichten eines elektrisch leitenden substrats.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19843432233 DE3432233A1 (de) 1984-09-01 1984-09-01 Kathodisch abscheidbares waessriges elektrotauchlackueberzugsmittel und verfahren zum beschichten eines elektrisch leitenden substrats
DEP3432233.7 1984-09-01

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WO1986001526A1 true WO1986001526A1 (en) 1986-03-13

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PCT/DE1985/000261 WO1986001526A1 (en) 1984-09-01 1985-08-02 Aqueous electrophoretic coating by cathodic deposition and method for coating an electric conductor substrate

Country Status (8)

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US (1) US4781808A (en, 2012)
EP (1) EP0214998B1 (en, 2012)
JP (1) JPS62500107A (en, 2012)
BR (1) BR8507240A (en, 2012)
CA (1) CA1317395C (en, 2012)
DE (2) DE3432233A1 (en, 2012)
ES (1) ES8703156A1 (en, 2012)
WO (1) WO1986001526A1 (en, 2012)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0249884A3 (en) * 1986-06-16 1988-10-26 Kansai Paint Co. Ltd. Resin composition for use in electrodeposition paints
DE3809695A1 (de) * 1988-03-23 1989-10-12 Hoechst Ag Haerter fuer kunstharze, diesen enthaltende haertbare mischungen sowie deren verwendung
EP0349873A3 (de) * 1988-07-04 1991-11-13 Vianova Kunstharz Aktiengesellschaft Verfahren zur Herstellung von Vernetzungskomponenten für Lackbindemittel
EP0403044A3 (en) * 1989-06-16 1992-01-02 Hunter Douglas Industries B.V. Blocked isocyanates and their production and use
EP0625530A1 (en) * 1993-05-17 1994-11-23 Nippon Paint Co., Ltd. Oxazolidone ring-containing modified epoxy resins and cathodic electrodeposition paints containing same
CN1066465C (zh) * 1994-03-22 2001-05-30 日本油漆株式会社 含嵌段异氰酸酯部分和阳离子基的改性环氧树脂和它们在阴极电沉积涂料中的应用

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DE3800474A1 (de) * 1988-01-11 1989-07-20 Basf Lacke & Farben Verfahren und vorrichtung zum messen der viskositaet von stoffen
DE3906143A1 (de) * 1989-02-28 1990-09-06 Basf Lacke & Farben Hitzehaertbares ueberzugsmittel fuer die kathodische elektrotauchlackierung
US5070149A (en) * 1990-04-09 1991-12-03 E. I. Du Pont De Nemours And Company Cationic resin composition with reduced emissions during baking
DE4015703A1 (de) * 1990-05-16 1991-11-21 Basf Lacke & Farben Verfahren zum beschichten elektrisch leitfaehiger substrate und kathodisch abscheidbarer waessriger elektrotauchlack
US5338479A (en) * 1991-02-12 1994-08-16 Cargill, Incorporated Blocked isocyanate blend having a high isocyanate content
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US5243011A (en) * 1992-04-09 1993-09-07 Cargill, Incorporated Low temperature curing, high solids, low VOC coating composition
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Publication number Priority date Publication date Assignee Title
EP0249884A3 (en) * 1986-06-16 1988-10-26 Kansai Paint Co. Ltd. Resin composition for use in electrodeposition paints
DE3809695A1 (de) * 1988-03-23 1989-10-12 Hoechst Ag Haerter fuer kunstharze, diesen enthaltende haertbare mischungen sowie deren verwendung
EP0349873A3 (de) * 1988-07-04 1991-11-13 Vianova Kunstharz Aktiengesellschaft Verfahren zur Herstellung von Vernetzungskomponenten für Lackbindemittel
EP0403044A3 (en) * 1989-06-16 1992-01-02 Hunter Douglas Industries B.V. Blocked isocyanates and their production and use
EP0625530A1 (en) * 1993-05-17 1994-11-23 Nippon Paint Co., Ltd. Oxazolidone ring-containing modified epoxy resins and cathodic electrodeposition paints containing same
CN1066465C (zh) * 1994-03-22 2001-05-30 日本油漆株式会社 含嵌段异氰酸酯部分和阳离子基的改性环氧树脂和它们在阴极电沉积涂料中的应用

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JPH027982B2 (en, 2012) 1990-02-21
BR8507240A (pt) 1987-10-27
ES8703156A1 (es) 1987-02-01
EP0214998A1 (de) 1987-03-25
US4781808A (en) 1988-11-01
EP0214998B1 (de) 1989-01-25
DE3567902D1 (en) 1989-03-02
CA1317395C (en) 1993-05-04
DE3432233A1 (de) 1986-03-13
JPS62500107A (ja) 1987-01-16
ES546621A0 (es) 1987-02-01

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