GB2156828A - Metallic coating compositions - Google Patents

Metallic coating compositions Download PDF

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Publication number
GB2156828A
GB2156828A GB08508867A GB8508867A GB2156828A GB 2156828 A GB2156828 A GB 2156828A GB 08508867 A GB08508867 A GB 08508867A GB 8508867 A GB8508867 A GB 8508867A GB 2156828 A GB2156828 A GB 2156828A
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United Kingdom
Prior art keywords
coating compositions
solvent
chemical compound
metallic
parts
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.)
Granted
Application number
GB08508867A
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GB8508867D0 (en
GB2156828B (en
Inventor
Christopher Henry Such
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.)
Dulux Australia Ltd
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Dulux Australia Ltd
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
Priority claimed from AU40756/85A external-priority patent/AU579857B2/en
Application filed by Dulux Australia Ltd filed Critical Dulux Australia Ltd
Publication of GB8508867D0 publication Critical patent/GB8508867D0/en
Publication of GB2156828A publication Critical patent/GB2156828A/en
Application granted granted Critical
Publication of GB2156828B publication Critical patent/GB2156828B/en
Expired legal-status Critical Current

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    • 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
    • C09D5/38Paints containing free metal not provided for above in groups C09D5/00 - C09D5/36
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/45Anti-settling agents

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

This invention relates to solvent-based coating compositions which comprise metal flake pigments. The disadvantages of known "metallic" finishes, e.g. haziness and mottle, can be overcome by the inclusion at the pigment dispersion stage of a chemical compound which comprises at least one hydroxyl group and at least one group of the formula <IMAGE> Coating compositions thus prepared are useful in the automotive and refinish industries.

Description

SPECIFICATION Coating compositions This invention relates to coating compositions and more particularly to solvent-based coating compositions which comprise metallic flake pigments.
The demand for so-called "metallic" finishes has increased constantly ever since such finishes were first introduced, this being particularly true of the automotive industry where their attractive appearance is much valued. The "metallic" effect is brought about by the inclusion in the coating composition of pigments which are minute flakes or plates of metal (usually aluminium).
Metallic flake pigments are generally incorporated into coating compositions by first dispersing the pigment in solvent alone, and then blending this dispersion with the film-forming medium and the other ingredients. I have now found that the addition to metallic finish coating compositions of certain chemical compounds makes possible the achievement of a "metallic" finish whose appearance is substantially better than that of known compositions.I therefore provide, according to the present invention a solvent-based coating composition which comprises metallic flake pigment wherein the metallic flake pigment is initially dispersed in solvent in the presence of a chemical compound which comprises at least one hydroxyl group and at least one group of the fomula
The chemical compound comprising at least one hydroxyl group and at least one group of the abovementioned formula may be derived, for example, from the compound e-caprolactone.
This ring will readily open in the presence of certain chemical species, for example, an active hydrogen atom, to give a linear hydrocarbon structure with an ester group. Other units of the abovementioned formula can readily be added on to form a long chain of the general formula
where X is the radical of a chemical compound comprising the chemical species which opened the -caprolactone ring. The number n can in theory be infinite, but there is a practical limit to the size of the molecule, this being dictated by its compatibility with the coating composition.
This type of linear molecule is not the only type of chemical compound which can be used.
For example, a polymer or pre-polymer comprising suitable chemical species may be used as the basis of a suitable chemical compound. The chemical species can act as reactive sites for a molecule such as e-caprolactone and the result is a chemical compound having a polymer/prepolymer "backbone" and a number of side chains made up of groups of the abovementioned formula.
Although chemical compounds having at least one group of the abovementioned formula will work in my invention, I have found that for best results, there should be sufficient groups present such that the compounds are waxy solids. In practice, this means that there should be a minimum of about 5 groups present.
A typical example of a suitable chemical compound for use in my invention is pentaerythritol which has been reacted with e-caprolactone to give a compound with 80 groups of the abovementioned formula. It is of course permissible to blend two or more chemical compounds.
The quantity of chemical compound to be used in the coating compositions can vary enormously, depending on the nature of the composition and the quantity and type of metallic flake pigment to be used. I believe, without restricting the scope of my invention in any way, that there must be sufficient present to coat completely the surface of the pigment particles. It is thus impossible to put precise limits of the quantity, but in general terms, most coating compostions will have between 5 and 30% by weight of the weight of the pigment.
The use of the compound caprnlactone is an especially convenient way of preparing chemical compounds for use in my invention but it is by no means the only way of doing so, and suitable compounds prepared by alternative synthetic routes will work in my invention.
This invention is applicable to any of the solvent-based film-forming coating systems known to the art, for example, acrylic lacquers and acrylic, alkyd, polyester and polyurethane enamels. It may -also be used to advantage in the so-called ' "basecoat/clearcoat" ' finishes, to enhance their already excellent appearance.
The invention is further illustrated by the following examples in which all parts are expressed by weight.
EXAMPLE 1 Preparation of a thermoplastic "metallic" coating composition according to the invention and comparison with a conventional material.
Aluminium flake pigment was dispersed in toluene and a dispersant in the following proportions; aluminium flake pigment 1.11 parts dispersant 0.20 parts toluene 2.04 parts (The dispersant was prepared by heating 1 mol of oleic acid, 40 mol of e-caprolactone and 0.2 mol dibutyl tin dilaurate for 2 hours at 1 70'C. It was a waxy solid at room temperature).
The abovementioned dispersion was blended with an acrylic copolymer, cellulose acetate butyrate (CAB) and butyl benzyl phthalate to give a coating composition whose non-volatile content was as follows: aluminium flake pigment 1.10 Parts dispersant 0.20 Parts 94/6 methyl methacrylate/ butylacrylate copolymer 44.27 Parts CAB (EAB 381-2 ex Eastman Chemicals) 27.21 Parts CAB (EAB 381-20 ex Eastman Chemicals) 3.89 Parts butyl benzyl phthalate 23.33 Parts The coating composition thus prepared was thinned to spraying viscosity and applied to phosphated and primed steel panels. A commerically-available silver metallic acrylic lacquer having a film-forming medium comprising a methyl methacrylate copolymer, CAB and butyl benzyl and butyl cyclohexyl phthalate plasticisers was also sprayed on to identical panels.Both sets of panels were baked for 10 minutes at 80'C, lightly sanded and then reflow baked for 30 minutes at 1 35'C to give smooth glossy films.
The low angle (20 ) gloss of both compositions were tested and they were also assessed for the surface "haze" characteristic of known single layer "metallic" finishes. The composition according to the invention had a 20 gloss of 80% with complete freedom from the "haze", whereas the commercial composition had a 20 gloss of 67% with considerable "haze".
EXAMPLE 2 Preparation of a series of chemical compounds.
The chemical compounds prepared were the reaction products of (a) 1 mol pentaerythritol with 80 mols e-caprolactone monomer; (b) 1 mol dibutylamine with 30 mols e-caprolactone monomer; and (c) 1 mol oleic alcohol with 30 mols e-caprolactone monomer The preparations were identical and were carried out using the method described below.
The reactants were charged to a reaction vessel and 0.5% by weight of dibutyl tin dilaurate catalyst was added. The mixture was heated to 170"C maximum and held there until reaction was complete (measured by solids content and free e-caprolactone content).
All three chemical compounds were low melting point waxy solids which were readily soluble in common organic solvents.
EXAMPLE 3 Preparation of coating compositions using the chemical compounds of Example 2.
The three chemical compounds prepared according to Example 2 were each used as dispersants for aluminium flake pigment according to the following formula: aluminium flake pigment 0.98 parts chemical compound 0.1 5 parts toluene 1.0 parts These ingredients were mixed and stirred slowly to achieve dispersion of the aluminium pigment. This dispersion was utilised in the preparation of a coating composition whose nonvolatile content was identical to that of Example 1.
The three coating compositions thus prepared were thinned to spraying visocisty and applied to phosphated and pimed steel panels. A commercially-available silver metallic acrylic lacquer having as film-forming medium methyl methacrylate copolymer, cellulose acetate butyrate and plasticisers was applied to identical panels. All panels were baked for 10 minutes at 80"C, lightly sanded and then reflow baked at 135"C for 30 minutes to give smooth, glossy films.
The 20 gloss of the panels was measured and they were assessed visually for freedom from spray mottle". The degree of "mottle" (the presence of irregularly shaped and randomly distributed areas of non-uniform colour) is a measure of the contro! of the aluminium particles during spraying. In this case, it was rated on a subjective numerical scale of 1-10, where 10 represents complete freedom from mottle and 1 represents extremely bad mottle.
20 gloss mottle rating commerical composition 68 5 composition with chemical compound (a) 77 9 compound (b) 78 8 compound (c) 77 9 The compositions according to the invention thus showed significantly higher gloss and freedom from mottle than the commerical coating composition.
EXAMPLE 4 Use of chemical compounds according to the invention in a basecoat/clearcoat finish.
Three chemical compounds were prepared according to the method of Example 2. These were the reaction products of (a) 1 mol pentaerythritol with 80 mols e-caprolactone monomer; (b) 1 mol trimethylol propane with 60 mols e-caprolactone monomer, and (c) 1 mol ethylene glycol with 40 mols e-caprolactone monomer.
These were each used to prepare dispersions of aluminium flake pigment by blending the following materials; aluminium flake pigment 1.7 parts chemical compound 0.6 parts toluene 2.0 parts A standard aluminium pigment dispersion was prepared by repeating the above-described preparation without the chemical compound.
The dispersions were each processed into thermoplastic coating compositions suitable as the basecoat of a basecoat/clearcoat composition by blending the following film-forming components; acrylic copolymer 1 6.5 parts cellulose acetate butyrate 6.4 parts plasticiser 7.3 parts The four compositions were thinned identically and applied to primed phosphated steel panels. When the panels were touch dry, they were coated with a commercially-available thermoplastic acrylic clearcoat and the finish air dried.
The panels were assessed subjectively for mottle control and gloss, assessment being made on a scale of from 1 (very bad) to 10 (excellent). The results were as follows: Gloss Mottle standard Al dispersion 6 6 dispersion with compound (a) 8 8 dispersion with compound (b) 8 8 dispersion with compound (c) 9 9 The coating compositions comprising chemical compounds according to the invention have superior properties even when coated with a conventional clearcoat.

Claims (5)

1. A solvent-based coating composition comprising metallic flake pigment, wherein the metallic flake pigment is initially dispersed in solvent in the presence of a chemical compound which comprises at least one hydroxyl group and at least one group of the formula
2. A solvent-based coating composition according to claim 1, where the group is derived from caprnlactone.
3. A solvent-based coating composition according to claim 1 wherein the chemical compound comprises at least 5 groups of the formula.
4. A solvent-based coating composition according to claim 1, wherein the quantity of chemical compound present in the composition is from 5-30% by weight of the metallic flake pigment.
5. A solvent-based coating composition substantially as hereinabove described with reference to any one of the examples.
GB08508867A 1984-04-06 1985-04-04 }metallic} coating compositions Expired GB2156828B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPG446384 1984-04-06
AUPG525484 1984-05-29
AU40756/85A AU579857B2 (en) 1984-04-06 1985-04-02 Coating composition comprising metallic flake pigment

Publications (3)

Publication Number Publication Date
GB8508867D0 GB8508867D0 (en) 1985-05-09
GB2156828A true GB2156828A (en) 1985-10-16
GB2156828B GB2156828B (en) 1987-06-03

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GB08508867A Expired GB2156828B (en) 1984-04-06 1985-04-04 }metallic} coating compositions

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0794237A2 (en) * 1996-03-04 1997-09-10 Basf Corporation Single stage paint compositions
EP0860484A2 (en) * 1997-02-24 1998-08-26 Silberline Manufacturing Co. Inc. Lamellar pigment particle dispersion
WO2006061635A1 (en) * 2004-12-08 2006-06-15 Aerochrome Limited Flake pigment mixture and multilayer coating method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2056461A (en) * 1979-07-26 1981-03-18 Ici Ltd Dispersible inorganic pigment
GB2147307A (en) * 1983-09-09 1985-05-09 Dulux Australia Ltd Thermo plastic coating compositions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2056461A (en) * 1979-07-26 1981-03-18 Ici Ltd Dispersible inorganic pigment
GB2147307A (en) * 1983-09-09 1985-05-09 Dulux Australia Ltd Thermo plastic coating compositions

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0794237A2 (en) * 1996-03-04 1997-09-10 Basf Corporation Single stage paint compositions
EP0794237A3 (en) * 1996-03-04 1997-10-01 Basf Corporation Single stage paint compositions
EP0860484A2 (en) * 1997-02-24 1998-08-26 Silberline Manufacturing Co. Inc. Lamellar pigment particle dispersion
EP0860484A3 (en) * 1997-02-24 1998-12-30 Silberline Manufacturing Co. Inc. Lamellar pigment particle dispersion
US6306931B1 (en) 1997-02-24 2001-10-23 Silberline Manufacturing Co., Inc. Lamellar pigment particle dispersion
WO2006061635A1 (en) * 2004-12-08 2006-06-15 Aerochrome Limited Flake pigment mixture and multilayer coating method
AU2005313105B2 (en) * 2004-12-08 2011-07-14 Aerochrome Limited Flake pigment mixture and multilayer coating method
US8017187B2 (en) 2004-12-08 2011-09-13 Aerochrome Limited Flake pigment mixture and multilayer coating method

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Publication number Publication date
GB8508867D0 (en) 1985-05-09
GB2156828B (en) 1987-06-03

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