DE3316550C2 - Process for priming plastics - Google Patents

Process for priming plastics

Info

Publication number
DE3316550C2
DE3316550C2 DE3316550A DE3316550A DE3316550C2 DE 3316550 C2 DE3316550 C2 DE 3316550C2 DE 3316550 A DE3316550 A DE 3316550A DE 3316550 A DE3316550 A DE 3316550A DE 3316550 C2 DE3316550 C2 DE 3316550C2
Authority
DE
Germany
Prior art keywords
plastics
polyacrylate
weight
priming
polyurethane
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.)
Expired
Application number
DE3316550A
Other languages
German (de)
Other versions
DE3316550A1 (en
Inventor
Frank 1000 Berlin Clasen
Karl-Heinz Weinert
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.)
Chemulack Chemische- und Lackfabrik & Co Kg 1000 Berlin De GmbH
Original Assignee
Chemulack Chemische- und Lackfabrik & Co Kg 1000 Berlin De 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 Chemulack Chemische- und Lackfabrik & Co Kg 1000 Berlin De GmbH filed Critical Chemulack Chemische- und Lackfabrik & Co Kg 1000 Berlin De GmbH
Priority to DE3316550A priority Critical patent/DE3316550C2/en
Priority to DE3440534A priority patent/DE3440534A1/en
Priority to DE19843440537 priority patent/DE3440537A1/en
Priority to DE19843440535 priority patent/DE3440535A1/en
Publication of DE3316550A1 publication Critical patent/DE3316550A1/en
Application granted granted Critical
Publication of DE3316550C2 publication Critical patent/DE3316550C2/en
Expired legal-status Critical Current

Links

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
    • C09D17/00—Pigment pastes, e.g. for mixing in paints
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
    • 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
    • C09D133/00—Coating compositions based on homopolymers or 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08—Homopolymers or copolymers of acrylic acid esters
    • 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
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2433/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2433/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2433/08—Homopolymers or copolymers of acrylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

Die Erfindung bezieht sich auf eine pigment- und bindemittelhaltige Mischung zum Grundieren von Kunststoffen. Die Erfindung besteht darin, daß das Bindemittel in Wasser dispergiertes, aliphatisches Polyurethan und in Wasser dispergiertes Polyacrylat ist. Eine solche Mischung greift Kunststoff nicht an und ist umweltfreundlich.The invention relates to a mixture containing pigments and binders for priming plastics. The invention consists in that the binder is aliphatic polyurethane dispersed in water and polyacrylate dispersed in water. Such a mixture does not attack plastic and is environmentally friendly.

Description

enthält, wobei das Verhältnis von Polyurethan zu Polyacrylat zwischen 70 :30 und 30 :70 liegtcontains, the ratio of polyurethane to polyacrylate between 70:30 and 30:70

2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man eine wäßrige Dispersion verwendet, in der das Verhältnis von Polyurethan zu Polyacrylat 50 :50 ist.2. The method according to claim 1, characterized in that that an aqueous dispersion is used in which the ratio of polyurethane to polyacrylate 50:50 is.

3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß man eine wäßrige Dispersion verwendet, die als Härter (d) ein Aikyl-Aziridin enthält.3. The method according to claim 1 or 2, characterized in that that an aqueous dispersion is used which contains an alkyl aziridine as hardener (d).

4. Verfahren nach Anspruch 1 bis 3, dadurch gekennzeichnet, daß man eine wäßrige Dispersion verwendet, in der der Festkörperanteil (a), (b) und (c), bezogen auf (a), (b), (c) und Wasser, 35-70 Gew.-%, insbesondere 52—58 Gew.-% beträgt.4. The method according to claim 1 to 3, characterized in that an aqueous dispersion is used, in which the solids content (a), (b) and (c), based on (a), (b), (c) and water, 35-70% by weight, in particular is 52-58% by weight.

5. Verfahren nach Anspruch 1 bis 4, dadurch gekennzeichnet, daß man eine wäßrige Dispersion verwendet, in der der Anteil des Härters (d), bezogen auf (a), (b), (c) und Wasser, 0,5—4 Gew.-%, insbesondere 2 Gew.-%, beträgt5. The method according to claim 1 to 4, characterized in that an aqueous dispersion is used, in which the proportion of hardener (d), based on (a), (b), (c) and water, 0.5-4% by weight, in particular 2% by weight

6. Verfahren nach Anspruch 1 bis 5, dadurch gekennzeichnet, daß man eine wäßrige Dispersion verwendet, die geringe Mengen eines organischen Lösungsmittels enthält6. The method according to claim 1 to 5, characterized in that an aqueous dispersion is used, which contains small amounts of an organic solvent

7. Verfahren nach Anspruch 1 bis 6, dadurch gekennzeichnet daß man eine wäßrige Dispersion verwendet, die zusätzlich einen Extender enthält, wobei dann der Festkörper aus 5—80Gew.-%, insbesondere 50Gew.-%, Pigment und Extender und 95—20 Gew.-%, insbesondere 50 Gew.-%, Polyurethan und Polyacrylat besteht.7. The method according to claim 1 to 6, characterized in that an aqueous dispersion is used, which additionally contains an extender, in which case the solids then consist of 5-80% by weight, in particular 50% by weight, pigment and extender and 95-20% by weight, especially 50% by weight, polyurethane and polyacrylate.

Bisher hat man Mischungen aus Polyurethan und Polyacrylat in organischen Lösungsmitteln zum Grundieren von Kunststoffen verwendet. Die Lösungsmittel wirken jedoch mehr oder weniger stark zerstörend auf die Kunststoffe ein. Hinzu kommt, daß das verdunstende Lösungsmittel umweltfeindlich ist.So far, mixtures of polyurethane and polyacrylate in organic solvents have been used for priming used by plastics. However, the solvents have a more or less destructive effect the plastics one. In addition, the evaporating solvent is harmful to the environment.

Weiterhin ist es aus der US-PS 42 78 578 bekannt, daß im Wasser dispergierte Polyurethane, welche ionische Gruppen enthalten, mit Härtern (Aziridinen) vernetzt werden können. Außerdem können die Dispersionen mit Acryl-, Alkyd- oder Vinyl-Latices gemischt werden. Ferner wird in der US-PS darauf hingeweisen, daß die polyfunktionellen Aziridine zum Vernetzen von Carboxylgruppen aufweisenden Polyacrylaten verwendet werden können (US-PS 42 78 578, Sp. 2, Z. 12-28). Aus diesem Stand der Technik ist zwar zu entnehmen, daß sowohl das genannte Polyurethan als auch das Carboxylgruppen aufweisende Polyacrylat jeweils für sich vernetzt werden können und daß die Mischung des dispergierten Polyurethans mit einem Acryllatex in einer unvernetzten Form zu Filmen mit günstigen Eigenschaften führt, jedoch konnte daraus nicht geschlossen werden, daß gerade die Mischung aus Carboxylgruppen enthaltendem Polyurethan und Carboxylgruppen enthaltendem Polyacrylat durch gemeinsame Vernetzung zu Produkten mit besonderen Verwendungseigenschaften führt und zwar zu Verwendungseigenschaften, die in der US-PS nicht einmal genannt sind, nämlich zur Grundierung von Kunststoffen.It is also known from US Pat. No. 4,278,578 that polyurethanes dispersed in water, which are ionic Contain groups that can be crosslinked with hardeners (aziridines). In addition, the dispersions mixed with acrylic, alkyd or vinyl latices. It is also pointed out in the US-PS that the polyfunctional aziridines are used for crosslinking polyacrylates containing carboxyl groups (US-PS 4,278,578, col. 2, lines 12-28). From this prior art it can be seen that both the polyurethane mentioned and the polyacrylate containing carboxyl groups are each crosslinked individually can be and that the mixture of the dispersed polyurethane with an acrylic latex in an uncrosslinked Form leads to films with favorable properties, but it could not be concluded from this that just the mixture of carboxyl-containing polyurethane and carboxyl-containing Polyacrylate through joint cross-linking to form products with special application properties leads to use properties that are not even mentioned in the US-PS, namely the primer of plastics.

Wie wenig das beanspruchte Verfahren durch die Lehre aus der US-PS nahegelegt wurde, ist auch daraus ersichtlich, daß in der US-PS zur Weiterentwicklung des dort genannten Standes der Technik nun eine Kombination verwendet wird, welche neben dem Härter (Aziridin) ein Carboxylgruppen aufweisendes Polyurethan, ein Carboxylgruppen aufweisendes Polyacrylat und als drittes Polymer einen mit einer monoäthylenivr? ungesättigten zweibasigen Säure modifizierten Ester eines Naturharzes oder ein Styrol-Maleinsäureanhydrid-Copolymerisat enthält Es wird also noch eine dritte Polymer-Komponente hinzugenommen, woraus an sich zu schließen ist daß mit der Mischung aus Polyurethan, Polyacrylat und Härter keine zufriedenstellenden Ergebnisse zu erhalten waren. Zudem wird auch die in der US-PS beanspruchte Zusammensetzung nicht zum Grundieren von Kunststoffen unter Verwendung eines Pigmentes, sondern zum Überziehen von Kunststoffen eingesetztHow little the claimed method was suggested by the teaching of the US patent is also therefrom It can be seen that in the US-PS for the further development of the prior art cited there now a combination is used, which in addition to the hardener (aziridine) is a carboxyl-containing polyurethane, a polyacrylate containing carboxyl groups and, as the third polymer, one with a monoäthylenivr? unsaturated dibasic acid-modified ester of a natural resin or a styrene-maleic anhydride copolymer It also contains a third polymer component, from which to itself The conclusion is that the mixture of polyurethane, polyacrylate and hardener does not give satisfactory results were to be obtained. In addition, the composition claimed in US Pat Priming of plastics using a pigment, but for coating plastics used

Aus dem Journal of Coated Fabrics, Vol. 3 (1974), S. 181 —193, insbesondere S. 186, ist es bekannt, daß einer wäßrigen Dispersion von Carboxylgruppen enthaltendem Polyurethan ein Pigment und — als Verdikkungsmittel — ein Polyacrylat zugesetzt werden können, wobei unterstellt werden kann, daß das Polyacrylat für seine Funktion als Verdickungsmittel Carboxylgruppen aufweist. Da in dieser Literaturstelle ein Härter nicht genannt ist und das Polyacrylat lediglich die Funktion eines Verdickungsmittels ausübt und somit auch nur in entsprechend geringen Mengen vorhanden sein dürfte, konnte aus dieser Literaturstelle ebenfalls nicht auf die gemeinsame Härtung von Polyurethan und Polyacrylat geschlossen werden und noch weniger auf die Eignung einer wäßrigen Dispersion aus jewiels Carboxylgruppen enthaltendem Polyurethan und Polyacrylat sowie Härter für das Grundieren von Kunststoffen, zumal dieser Verwendungszweck in der Literaturstelle gar nicht genannt ist.
Der Erfindung liegt die Aufgabe zugrunde, ein Verfahren zum Grundieren von Kunststoffen zu schaffen, bei dem einerseits der Kunststoff nicht angegriffen wird und daj andererseits umweltfreundlich istFrom the Journal of Coated Fabrics, Vol. 3 (1974), pp. 181-193, in particular p. 186, it is known that a pigment and - as a thickening agent - a polyacrylate can be added to an aqueous dispersion of polyurethane containing carboxyl groups, it can be assumed that the polyacrylate has carboxyl groups for its function as a thickener. Since a hardener is not mentioned in this reference and the polyacrylate only functions as a thickener and is therefore only likely to be present in correspondingly small quantities, this reference also did not allow conclusions to be drawn about the joint hardening of polyurethane and polyacrylate, and even less the suitability of an aqueous dispersion of polyurethane and polyacrylate each containing carboxyl groups as well as hardeners for priming plastics, especially since this purpose is not mentioned in the reference.
The invention is based on the object of creating a method for priming plastics in which, on the one hand, the plastic is not attacked and, on the other hand, is environmentally friendly

Diese Aufgabe wird erfindungsgemäß durch das im Anspruch 1 genannte Verfahren gelöst, wobei die Ausgestaltungen dieses Verfahrens in den Ansrüchen 2—7 beschrieben sind.According to the invention, this object is achieved by the method mentioned in claim 1, with the embodiments this method are described in claims 2-7.

Es wird somit eine pigment- und bindemittelhaltige Mischung zum Grundieren von Kunststoffen verwendet, deren Bindemittel durch in Wasser dispergiertes, aliphatisches Polyurethan und in Wasser dispergiertes Polyacrylat gekennzeichnet ist.A mixture containing pigments and binders is used to prime plastics, their binders by aliphatic polyurethane dispersed in water and dispersed in water Polyacrylate is marked.

Als Polyurethane und Polyacrylate kommen all jene Stoffe in Frage, die in Wasser dispergiert (als Dispersion oder Hydrosol) sind, obheralb von 00C filmbildende Eigenschaften aufweisen, pigmentverträglich und lagerstabil sind und die reaktionsfähige Carboxylgruppen enthalten. Ferner müssen beide Produkte scherkraftstabi! sein, um auf handelsüblichen Dispergiergeräten (z. B.As polyurethanes and polyacrylates those are suitable are dispersed in water (as a dispersion or hydrosol) obheralb film-forming from 0 0 C properties, are compatible and storage stable pigment and containing reactive carboxyl groups. Furthermore, both products must be shear-resistant! in order to be able to use commercially available dispersing devices (e.g.

PerimOhlen) verarbeitet werden zu können.PerimOhlen) to be processed.

Zur Herstellung der zu verwendenden Grundierungsmjttel werden Polyurethan-Dispersionen eingesetzt, die bei einem Festkörpergehalt (Gew.-%) von 25—50%, vorzugsweise 35—40%, eine Konsistenz von < 1000 mPas, vorzugsweise 100—500 mPas, aufweisen. Das Polyacrylat-Hydrosol hat bei einem Festkörperanteil in Gew.-% von 35—55%, vorzugsweise 45%, eine Konsistenz von < 400 mPas, vorzugsweise <200mPas.To produce the primers to be used, polyurethane dispersions are used which at a solids content (% by weight) of 25-50%, preferably 35-40%, a consistency of <1000 mPas, preferably 100-500 mPas. The polyacrylate hydrosol has a solids content in% by weight of 35-55%, preferably 45% Consistency of <400 mPas, preferably <200mPas.

In der srfindungsgemäß verwendeten Mischung be- ίο trägt der Festkörperanteil 35—70 Gew.-%, insbesondere 52-58 Gew.-%.In the mixture used according to the invention be ίο the solids content is 35-70% by weight, in particular 52-58% by weight.

Der Flüssigkeitsanteil braucht nicht nur aus Wasser zu bestehen, sondern er kann auch aus 75—99 Gew.-%, insbesondere 81—92Gew.-%, Wasser und 25—1 Gew.-%, insbesondere 19—8Gew.-%, organischen Lösungsmitteln und zugesetztem Neutralisationsmittel bestehen.The liquid part need not only consist of water, but it can also consist of 75-99% by weight, in particular 81-92% by weight, water and 25-1% by weight, in particular 19-8% by weight, organic solvents and added neutralizing agent.

Eine solche vollständig oder weitgehend von Lösungsmitteln organischer Art freie Dispersion greift den Kunststoff, der gradiert wird, nicht an. Hinzu kommt, daß die Dispersion keine Verunreinigung der Atmosphäre bewirken kann.Such a dispersion which is completely or largely free of solvents of an organic nature takes effect Plastic that is graded is not on. Come in addition, that the dispersion cannot cause pollution of the atmosphere.

Die Dispersion kann mit und ohne Härtungsbeschleuniger verwendet werden. Als Pigment können die sonst üblichen Pigmente eingesetzt werden.The dispersion can be used with or without a hardening accelerator. As a pigment they can otherwise customary pigments are used.

Die wäßrige Dispersion kann durch die üblichen Verfahren aufgetragen werden.The aqueous dispersion can be applied by the usual methods.

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Claims (1)

Patentansprüche:Patent claims: 1. Verfahren zur Grundierung von Kunststoffen, dadurch- gekennzeichnet, daß man als Grundierungsmittel eine wäßrige Dispersion verwendet, welche1. A method for priming plastics, characterized in that as Primer uses an aqueous dispersion, Which (a) ein aliphatisches, reaktionsfähige Carboxylgruppen aufweisendes Polyurethan,(a) an aliphatic, reactive polyurethane containing carboxyl groups, (b) ein reaktionsfähige Carboxylgruppen aufweisendes Polyacrylat(b) a reactive polyacrylate containing carboxyl groups (c) ein Pigment und gegebenenfalls(c) a pigment and optionally (d) einen Härter(d) a hardener
DE3316550A 1983-05-03 1983-05-03 Process for priming plastics Expired DE3316550C2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
DE3316550A DE3316550C2 (en) 1983-05-03 1983-05-03 Process for priming plastics
DE3440534A DE3440534A1 (en) 1983-05-03 1984-11-02 Process for coating plastics
DE19843440537 DE3440537A1 (en) 1983-05-03 1984-11-02 Process for coating plastic parts
DE19843440535 DE3440535A1 (en) 1983-05-03 1984-11-02 Process for priming plastics

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE3316550A DE3316550C2 (en) 1983-05-03 1983-05-03 Process for priming plastics
DE3440534A DE3440534A1 (en) 1983-05-03 1984-11-02 Process for coating plastics
DE19843440537 DE3440537A1 (en) 1983-05-03 1984-11-02 Process for coating plastic parts
DE19843440535 DE3440535A1 (en) 1983-05-03 1984-11-02 Process for priming plastics

Publications (2)

Publication Number Publication Date
DE3316550A1 DE3316550A1 (en) 1984-11-08
DE3316550C2 true DE3316550C2 (en) 1985-07-25

Family

ID=37831451

Family Applications (4)

Application Number Title Priority Date Filing Date
DE3316550A Expired DE3316550C2 (en) 1983-05-03 1983-05-03 Process for priming plastics
DE19843440537 Ceased DE3440537A1 (en) 1983-05-03 1984-11-02 Process for coating plastic parts
DE19843440535 Ceased DE3440535A1 (en) 1983-05-03 1984-11-02 Process for priming plastics
DE3440534A Ceased DE3440534A1 (en) 1983-05-03 1984-11-02 Process for coating plastics

Family Applications After (3)

Application Number Title Priority Date Filing Date
DE19843440537 Ceased DE3440537A1 (en) 1983-05-03 1984-11-02 Process for coating plastic parts
DE19843440535 Ceased DE3440535A1 (en) 1983-05-03 1984-11-02 Process for priming plastics
DE3440534A Ceased DE3440534A1 (en) 1983-05-03 1984-11-02 Process for coating plastics

Country Status (1)

Country Link
DE (4) DE3316550C2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3316550C2 (en) * 1983-05-03 1985-07-25 Chemulack Chemische- Und Lackfabrik Gmbh & Co Kg, 1000 Berlin Process for priming plastics
WO1986002655A1 (en) * 1984-11-02 1986-05-09 Chemulack Chemische-Und Lackfabrik Gmbh & Co. Kg Process for providing plastics with a primer
DE3628125A1 (en) * 1986-08-19 1988-03-03 Herberts Gmbh AQUEOUS COATING AGENT, METHOD FOR THE PRODUCTION THEREOF AND THE USE THEREOF
US4889762A (en) * 1986-12-26 1989-12-26 Mitsui Petrochemical Industries Ltd. Molded articles of thermoplastic elastomer
EP0350157B2 (en) * 1988-05-30 1997-12-17 Dainippon Ink And Chemicals, Inc. Aqueous coating composition
DE3844435C1 (en) * 1988-12-31 1990-08-23 Kurz, Geb. Sendtko, Waldtraud, 8011 Vaterstetten, De
ZA913801B (en) * 1990-05-21 1993-01-27 Dow Chemical Co Latent catalysts,cure-inhibited epoxy resin compositions and laminates prepared therefrom
US5916960A (en) * 1993-12-21 1999-06-29 The Sherwin-Williams Company Water-based, storage stable, self-curing coating composition
US6180181B1 (en) 1998-12-14 2001-01-30 Ppg Industries Ohio, Inc. Methods for forming composite coatings on substrates
US6613830B2 (en) * 1999-01-29 2003-09-02 Michael J. Stevenson Aqueous base coating composition for polyolefin surfaces
US20150104635A1 (en) * 2013-10-14 2015-04-16 Ticona Llc Coatings for polyoxymethylene polymer molded articles
CN104212321B (en) * 2014-07-31 2016-04-20 昆山市大地化工新技术开发有限公司 Two component multifunctional type priming paint of PU and preparation method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2551094A1 (en) * 1975-11-14 1977-05-26 Bayer Ag PROCESS FOR THE MANUFACTURING OF WATER DISPERSIBLE POLYURETHANES
US4278578A (en) * 1979-11-05 1981-07-14 Hillyard Enterprises, Inc. Coating composition for synthetic plastic substrates and methods for preparing and using same
US4301053A (en) * 1980-01-29 1981-11-17 General Electric Company Polyurethane resin coating composition
DE3316550C2 (en) * 1983-05-03 1985-07-25 Chemulack Chemische- Und Lackfabrik Gmbh & Co Kg, 1000 Berlin Process for priming plastics

Also Published As

Publication number Publication date
DE3316550A1 (en) 1984-11-08
DE3440535A1 (en) 1986-05-07
DE3440537A1 (en) 1986-05-07
DE3440534A1 (en) 1986-05-07

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