CA1152670A

CA1152670A - Aqueous coating compositions for wood surfaces

Info

Publication number: CA1152670A
Application number: CA000363044A
Authority: CA
Inventors: Herbert Zima; Laszlo Tulacs
Original assignee: Vianova Resins AG
Current assignee: Allnex Austria GmbH
Priority date: 1979-11-09
Filing date: 1980-10-23
Publication date: 1983-08-23
Also published as: AT365218B; EP0029144B1; ATA719379A; DE3061641D1; US4366282A; EP0029144A1

Abstract

ABSTRACT
The present invention is concerned with aqueous coating compositions for wood surfaces which can be used to obtain clear open-pore or closed pore coatings. The coatings are based on polymer dispersions containing N-methylol acrylamide units, which optionally can be processed together with a basic paint based on a water soluble acrylic copolymer.

Description

6~i'0 The painting of wood with clear varnishes is described in detail in "Lehrbuch der Lacke und Beschichtungen", H. Kittel, vol. V, pages 305 - 317, edition W.A. Colomb, 1977. As said there, for this purpose mainly nitrocellulose lacquers ~cellulose nitrate lacquers, shortly called NC-lacquers) and acid cur-ing alkyd-amine resin enamels, polyurethane paints and paints based on unsatu-rated polyesters are used. All these coating compositions require a large amount of organic solvents for processing and application or of polymerisable monomers, which, some of which have a narcotic effect.
Thus, nowadays, there is a pronounced need for coating compositions based on water as a solvent, which does not mean environmental pollution, and where the paints correspond to nitrocellulose lacquers in performance.
Polymer dispersions containing N-methylol acrylamide units are known in the literature for various purposes.
United States patent specification 3,856,734 describes the preparation of dispersions from vinylacetate, N-methylol acrylamide and acrylic acid. The dispersions are used as adhesive for plywood.
According to United States patent specification 3,790,520, acrylic dispersions, besides the normal acrylates or methacrylates also optionally con-taining N-methylol acrylamide, are used in the textile industry, and for the surface protection of plastics, metal or wood.
The dispersions described in Deutsche Auslegeschrift 1,047,431 also contain methylol acrylamide units which are used for crosslinking the particles during production of the dispersion.
Deutsche Offenlegungsschrift 2,535,660 describes the preparation of auto-crosslinking polymer dispersions containing methylolated carboxylic acid amides and polymer solutions, wherein emulsion polymers containing acrylamide are produced which are subsequently reacted with methylolated carboxylic acid ., - 1 - ~.

~Z~'70 amides.
These known dispersions, when stoved at the conditions applicable to wood, give coatings which do not meet the requirements of practical use, neither `-with regard to mar resistance, hardness and flexibility nor with regard to what may be termed pile strength.
It is the task of the present invention to provide coating compositions for wood surfaces, particularly for furniture coating, replacing the normal nitro-cellulose lacquers and containing the lowest possible content of organic solvents.
The furniture industry requires such coatings to exhibit, on short cure at from 70 - 90C, great hardness and mar resistance in order to allow the objects to be piled within a short time and without damage to the coated surface.
Thus the coatings must exhibit an adequate pile strength. Furthermore, the coat-ing should not mask but bring out wood grain and colour and should have a high resistance, particularly to water.
These requirements can be met with the present invention through poly-mer dispersions which contain copolymers with high glass transition temperatures, in conjunction with speci~ically selected coalescing agents, and by providing an auto-crosslinking mechanism.
The present invention is thus concerned with polymer dispersions con-taining N-methylol acrylamide, consisting of 30 - 65 % by weight of methylmethacrylate 10 - 17 % by weight of ethylacrylate 10 - 30 % by weight of butylmethacrylate 5 - 20 % by weight of styrol 3 - 10 ~ by weight of N-methylol(meth)acrylamide and containing as coalescing agent 5 to 15 % by weight (of the dispersion~ of a blend consisting of 1~5~6'70 20 - 65 % by weight of a high boiling paint solvent such as 2,2,4-trimethylpen-tane-1,5-diol-mono-trimethylacetate and 80 - 35 % by weight of ethylene glycol monoethyletheracetate, and/or ethylene glycol monobutyletheracetate, optionally in conjunction with basic varnishes on the basis of cationic water soluble acrylic copolymers, for open pore or closed pore coatings for wood sur-faces.
In a particularly advantageous embodiment of the invention the disper-sions consist of 45 - 55 % by weight of methylmethacrylate 12 - 15 % by weight of ethylacrylate 15 - 25 % by weight of butylmethacrylate 5 - 10 % by weight of styrol 7 - 9 % by weight of N-methylol methacrylamide with the addition of a coalescing agent consisting of (calculated on the emulsicn) 4 - 6 % by weight of the mentioned high boiling paint solvent, 7 - 9 % by weight of ethylene glycol monoethylether acetate or 3 - 5 % by weight of ethylene glycol monobutylether acetate.
The coating compositions of the invention, after drying for 5 to 10 minutes at 75 to 90C, form coatings on wood which show excellent appearance, excellent hardness and mar resistance, and very good water resistance. The over-all performance is in all cases equal to the optimum of a nitrocellulose lacquer, with the additional essential advantage of non-flammability and non-toxicity.
The toxicity rating of the dispersions of the invention corresponds to YSAM, group 0. Furthermore, pile strength of the coatings is excellent after short cooling subsequent to the curing procedure. They are particularly suited for open pore coatings.

6'~0 The preparation of the polymer dispersions is effected in known manner by emulsion polymerisation, in the presence of anionic and non-ionic emulsifiers and free radical initiators. Water and the emulsifiers are charged to the poly-merisation reactor and heated to 85 to 88C and from 3 separate addition funnels monomer blend, methylolmethacrylamide and initiator solution are added simulta-neously over a period of 90 minutes. After the end of the addition, the batch is allowed to react at 88 to 90C for about 40 minutes.
The polymer dispersions of the invention are prepared from 30 - 65, preferably 45 - 55 % by weight of methylmethacrylate 10 - 17, preferably 12 - 15 % by weight of ethylacrylate 10 - 30, preferably 15 - 25 % by weight of butylmethacrylate 5 - 20, preferably 5 - 10 % by weight of Styrol and 3 - 10, preferably 7 - 9 % by weight of N-methylol~meth)acrylamide.
Suitable anionic emulsifiers are alkylarylethoxylate sulfates, the sul-fates of ethoxylated fat alcohols, dodecylbenzol sulfonate, or sulfosuccinamates.
With advantage, also non-ionic emulsifiers, such as ethoxylated alkylphenols, are used in conjunction with the anionic emulsifiers. Furthermore, also small quantities of sodium vinyl sulfonate can be copolymerised as additional emulsi-fier.
Suitable coalescing agents are blends of 2,2,4-trimethylpentane-1,5-diolmonotrimethyl acetate with ethylene glycolmonoethylether acetate or with ethyleneglycolmonobutylether acetate in a ratio of between 20 : 80 and 65 : 35.
The coalescing agents are mixed before addition and the blend is very slowly ad-ded to the dispersion while stirring well. Storage stability of the dispersion, also with the coalescing agents, is very good. The level of coalescing agents is from 5 to 15 % by weight of the dispersion.
It is the optical appearance of the clear varnish coated wood, such as 6'~0 the accentuation of the grain and the uniformity of the coating which may be still further enhanced through the use of a basic varnish of special water solu-ble acrylic copolymers.
The acrylic copolymers suitable for this purpose are amine adducts of copolymers carrying glycidyl groups, which can be rendered water soluble owing to neutralisation of their cationic groups with inorganic or organic acids. The copolymers have the following monomer composition:
20 - 40 % by weight of glycidylmethacrylate 40 - 80 % by weight of methylmethacrylate 0 - 40 % by weight of other (cyclo)alkylmethacrylates, the homopolymers of which have glass transition temperatures of over + 40C.
The copolymers produced in known manner are reacted with secondary amines carrying 1 or 2 hydroxyalkyl radicals, the ratio being 1 mole of a second-ary amine per 1 glycidyl group. The copolymers for the basic paint are prepared in known manner through solution polymerisation in ethanol or isopropanol. The method is to add the monomer blend mixed with the chain transfer agent to the charged solvent and initiator. When a conversion of practically 100 % is reached, the amine is slowly added in drops at 80 - 85C. The obtained adduct is prac-tically infinitely dilutable with water upon neutralisation with an organic or inorganic acid.
Suitable amines are secondary mono- or dialkanol amines, such as di-ethanol amine, di-~iso) propanol amine, cyclohexylethanol amine or ethylethanol amine. The basic paint shows excellent penetration of the wood and, upon dry-ing at normally applied conditions of 3 - 10 minutes at 70 - 90C, has the hard-ness, flexibility and sanding characteristics as required by the industry.
The polymer dispersions and the optionally used basic paint can be applied by brushing, curtain coating, spray gun, etc.
The following examples illustrate the invention without limiting the ~1~2~'70 scope of it. Parts and percentages are by weight.
Example 1:
In a polymerisation reactor equipped with reflux condensor, thermometer and inert gas supply, a batch is charged consisting of 1322 parts of deionised water, 18 parts of the sodium salt of an octylphenol reacted with 2 moles of ethyl-ene oxide and sulfated, 12 parts of an octylphenol reacted with 16 moles of ethyl-ene oxide and 7.2 parts of sodium vinyl sulfonate. The charge is heated to 85 -87C. While continuously stirring, the following ingredients are added simulta-neously, from 3 separate addition funnels, within a period of 90 minutes:
1. monomer blend consisting of 645 parts of methylmethacrylate, 267 parts of n-butylmethacrylate, 180 parts of ethylacrylate and 66 parts of styrol,

2. 246 parts of a 36 % aqueous solution of N-methylolmethacrylamide,

3. a solution of 3 parts of ammonium peroxodisulfate in 90 parts of water.
During polymerisation a temperature of 86 - 88C is maintained. After the end of the monomer addition, the batch is reacted at 88 - 90C for another 40 minutes.
The dispersion is cooled, and, while stirring well, a blend of 143 parts of a paint solvent on the basis of 2,2,4-trimethylpentane-1,5-diol mono-trimethylacetate (boiling range 180 - 182C, at 125 mm Hg, f. i. Texanol C~ of EASTMAN KODAK PROD. INC.) and 228 parts of ethyleneglycolmonoethylether acetate or 114 parts of butyletheracetate is added.
A stable, fine particle dispersion of about 41 % solids is obtained.
For testing, it is applied to various types of wood, i.e. oak, walnut and maho-gany panels, by spraying and curtain coating. After a flash-off of 1 minute the coats are dried at 85C for 5 minutes.
The obtained coatings have a film thickness of about 30 ~m. They are very hard, have good mar resistance and an excellent appearance. The Buchholz ~15;~6'70 test (Erichsen, DIN 53 153) gives a value of 1.7 mm. Colour and wood grain of all types of wood are accentuated considerably.
Example 2:
The process of example 1 is repeated using a bath of 1268 parts of de-ionised water, 18 parts of the sodium salt of an octylphenol reacted with 2 moles of ethylene oxide and sulfated, 12 parts of an octylphenol reacted with 16 moles of ethylene oxide and 7.2 parts of sodium vinylsulfonate. At 85 - 87C the fol-lowing ingredients are added:
1. monomer blend of 481 parts of methylmethacrylate, 342 parts of n-butylmeth-acrylate, 144 parts of ethylacrylate and 156 parts of styrol;
2. 282 parts of a 36 % aqueous solution of N-methylolmethacrylamide;
3. a solution of 3 parts of ammonium peroxodisulfate in 90 parts of water.
The coalescing agent in this case is a blend of 111 parts of the high boiling solvent used in example 1 and 84 parts of ethylene glycol monobutyl-etheracetate.
The obtained dispersion has the same properties as that obtained accord-ing to example 1.
The water soluble cationic copolymers used in suitable base paints are prepared as follows.
In a reactor equipped with stirrer, thermometer and reflux condensor, 40 parts of isopropanol containing dissolved 2.5 parts of azobisisobutyronitrile, are charged and heated to about 80C. Then the monomer blends listed in table 1 are added, and 2 parts of dodecyl mercaptan or a solution of 2.5 parts of azo-bisisobutyronitrile in 20 parts of isopropanol and ethyl acetate (1:1) are added simultaneously and continuously from separate vessels. The addition is made at such a rate as to guarantee a conversion of 90 % at any time of the polymerisation.
The polymerisation is finished, when, at the end of the addition, the polymer ~15;~670 content corresponds to a conversion of 98 - 100 %. Then, at 40 - 50C, a solu-tion of diisopropanol amine in isopropanol is added slowly, as listed in table 1.
The exothermic reaction is monitored such that the temperature does not exceed 80C. After the end of the addition, a temperature of 80 to 85C is held for 2 hours.
Table 1:
Copolymer A B C D E F G H
monomer blend:

BMA ~~ 10 -- 10 -- 10 10 --amine solution DIPA 23,4 18,7 18,7 18,7 18,7 37,5 18,7 18,7 MMA : Methylmethacrylate BMA : Butylmethacrylate IMA : Isobutylmethacrylate TBA : Tert.-butylacrylate GMA : Glycidylmethacrylate DIPA : Diisopropanolamine IP : Isopropanol In examples B and C tert.butylperhexanoate was used instead of azo-bisisobutyronitrile.
The copolymers have a slightly yellow colour and are infinitely dilut-11~i2670 able with water upon neutralisation with acetic acid to a pH-value of from 4 to 6.
In preparing a base paint the resin solution is neutralised with diluted acetic acid (about 30 %) to a pH-value of from 5 to 6 and diluted with deionisedwater to a solid content of 15 to 30 %.
The wood types mentioned in example 2 were coated with a double coat system, the base coat consisting of the copolymers A - H of table 1. The finish-ing coats were the dispersions of examples 1 and 2.
The base coat was applied in a quantity of about 30 g/m2 and dried for 5 minutes at 85C. The coated surface could be sanded well ~emery paper no.
P 320). After sanding, the top dispersion coat was applied and also cured for 5 minutes at 85C. The coating with a thickness of 30 ~m had an excellent appear-ance, with fine gloss and great hardness and mar resistance. The differences between the various coatings were only slight. Piled panels did not stick together, even with loads. The Buchholz test gave a result of 1.7 mm in all cases. Colour and wood grain were strongly accentuated. The performance of the coatings cor-responds to that of an optimum quality nitrocellulose lacquer. On water soak a slight swelling could be observed after 2 hours.
~:.
Practically the same results were obtained with dispersions prepared according to the method of example 1 from 1314 parts of deionised water, 18 parts of the sodium salt of an octylphenol reacted with 2 moles of ethylene oxide and sulfated, 12 parts of an octylphenol reacted with 16 moles of ethylene oxide and7.2 parts of sodium vinyl sulfonate, with the following 3 components:
1. monomer blend of 697 parts of methylmethacrylate, 192 parts of n-butylmeth-acrylate, 180 parts of ethylacrylate and 60 parts of styrol;
2. 203 parts of a 36 % aqueous solution of N-methylolmethacrylamide;

~ . _ g _ , ~152670 3. a solution of 3 parts of ammonium peroxodisulfate in 90 parts of water.
The coalescing agent is a blend of 139 parts of the high boiling paint solvent used in example 1 and 194 parts of ethylene glycol monoethyletheracetate.

Claims

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. Polymer dispersions containing N-methylol(meth)acrylamide consist-ing of 30 - 65 % by weight of methylmethacrylate 10 - 17 % by weight of ethylacrylate 10 - 30 % by weight of butylmethacrylate 5 - 20 % by weight of styrol 3 - 10 % by weight of N-methylol(meth)acrylamide and containing as coalescing agent 5 to 15 % by weight (of the dispersion) of a blend consisting of 20 - 65 % by weight of a high boiling paint solvent of the type of 2,2,4-trimethylpentane-1,5-diol-mono-trimethyl acetate and 80 - 35 % by weight of ethyleneglycol monoethyletheracetate, and/or ethyleneglycolmonobutylether acetate.

2. Dispersions according to claim 1 containing from 45 - 55 % by weight of methylmethacrylate 12 - 15 % by weight of ethylacrylate 15 - 25 % by weight of butylmethacrylate 5 - 10 % by weight of styrol 7 - 9 % by weight of N-methylol methacrylamide with the addition of a coalescing agent consisting of (calculated on the emulsion) 4 - 6 % by weight of the high boiling paint solvent, 7 - 9 % by weight of ethylene glycol monoethylether acetate or 3 - 5 % by weight of ethyleneglycolmonobutylether acetate.

3. Dispersion according to claim 1 additionally containing an aqueous solution of a cationic amine adduct of copolymers carrying glycidyl groups.

4. Dispersion according to claim 3 wherein the cationic amine adduct is prepared from:
20 - 40 % by weight of glycidylmethacrylate 40 - 80 % by weight of methylmethacrylate 0 - 40 % by weight of other (cyclo)alkylmethacrylates, the homopolymers of which have a glass transition temperature of over + 40°C.

5. A method of coating wood surfaces which comprises applying thereto a polymer dispersion as claimed in claims 1, 2 or 3.