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    • 专利摘要:
    1330992 Coating compositions VIANOVA KUNSTHARZ AG 16 June 1971 [22 July 1970] 28303/71 Addition to 1229759 Headings C3G C3P and C3R [Also in Division C7] Coating compositions, for use in conventional or electrodeposition processes, comprise (A) the product obtained by reacting a diene polymer with an α,#-ethylenically unsaturated component and then esterifying up to 70% of the present or latent carboxyl groups with a monohydric alcohol, and (B) the reaction product of formaldehyde with a phenol carboxylic acid; and optionally (C) a polyhydroxy compound of M.W. 50-3000 or a derivative thereof; together with water, a water-tolerant solvent, pigments &c. if desired. In the specific examples, the following components are used: (A) products obtained by partial esterification, with methanol or ethylene glycol monomethyl ether, an adduct of maleic anhydride with either polybutadiene or a graft polymer of vinyl toluene on polybutadiene, the maleic anhydride adduction being conducted in the presence of either copper naphthenate or diphenyl-p-phenylene diamine; (B) the reaction products of formaldehyde with (i) 4,4 - bis - (4 - hydroxyphenyl) pentanoic acid, (ii) a phenol carboxylic acid formed from monochloracetic acid and 2,2-bis-(4-hydroxyphenyl) propane or (iii) a phenol carboxylic acid formed from monochloracetic acid and p-tertbutyl phenol; (C) an allyl alcohol/styrene copolymer or diethoxy diphenylolpropane; solvents: ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, isophorone and isopropanol; pigments &c.: mixture of aluminium silicate, TiO 2 and either red iron oxide or carbon black; and water, the pH of the compositions being adjusted as desired with NH 3 , triethylamine or KOH. The compositions are used to coat phosphated steel plate (as anode) by electrodeposition or steel coils by roller application. The coatings are cured by heating.
    公开号:SU738515A3
    申请号:SU711680552
    申请日:1971-07-08
    公开日:1980-05-30
    发明作者:Даймер Вольфганг；Клинчар Герфрид；Вердино Хейнер
    申请人:Вианова Кунстхарц Аг (Фирма)；
    IPC主号:
    专利说明:

    (54) PAINT AND VARNISH COMPOSITION
    The invention relates to paints and varnishes, coatings based on which have a high resistance to corrosion. Known paint composition vklyuchakhtsa reaction product I - diene polymer, p-unsaturated carboxylic acid or dikarbonsEvry acid or anhydride or half ester or semi-amides, Product II thermosetting phenol-formaldehyde resin obtained by formaldehyde condensation with phenol or fenokarbonovoy acid, and the solvent 1. The disadvantage A known composition is the low corrosion resistance of the coating. . In order to improve the corrosion resistance of the coating, they propose a composition which as product I contains the product of the interaction of a diene polymer with cX, p, unsaturated carboxylic acid, OR dicarboxylic acid, OR its anhydride, or half-ester, OR semi-amber, containing 50-70 esterified carboxyl groups at the following the ratio of products I and II, calculated on the dry matter, S; Product I70-95 30- 5.0 Product II Due to the partial esterification of product I, the proposed composition has a reduced tendency to self-oxidation. After neutralization with an alkaline agent, the proposed composition is water soluble. A polyhydroxyl compound can be added to the composition, a compound containing at least two hydroxyl groups and having a gel weight of from 50 to 3000. Diene polymers that are abbreviated polymers should be understood as diens, for example 1,3-AND / OR 2-methylbutadiene-1,3, AND / OR 2,3-dimethylbutadiene-1,3 and / or chloropropene in butadiene and so on, under certain conditions, with other mixed polymerizable monomers, t such as styrene, (α-methylstyrene, ortho, meta- or parachlorstyrene, vinyl naphthalene, vinylcyclohexane, vinylcyclohexene, vinyl acetate, COMPLEX ester of (meth) acrylic acid, (meth) acrylonitrile, and so on. They have molecular weights between. and 20,000 and contain predominantly double bonds that, under certain conditions, can be partially hydrated. Also, it is possible to modify the polymers with suitable diene by graft copolymerization with styrene, vinyl toluene (A-methyl styrene, ester (meth) acrylic kit lots, acrylnitrile others in order to obtain extremely high electrically insulating; properties obtained by anodic deposition of film-forming substances.
    As "L, ethylene-non-saturated carboxylic acids can be added:.
    (meth) acrylic acid, maleic acid, maleic anhydride, umaronic acid, itaconic acid. Using the complex half-ester maleinone acid, the temperatures of the reaction with ienpolymerization agent are recycled into maleic anhydride with simultaneous removal of the alcohol.
    For the preparation of component I, the dienes polymer is heated and, preferably, the maleic acid anhydride used is heated to 150-250 °, until complete fermentation. anhydrous Then, the formed addition process is subjected to reaction in a reflux vessel with mono alcohol. Catalysts, preferably tertiary amines, can be used to accelerate the reaction. The reaction temperature may be higher than the boiling point of the alcohol used. Over the course of the reaction
    followed by determining the acid value.
    Sootvetstvunadimi monoalcohols are all alkanols, e.g., methanol, ethanol, n-propanol, isopropanol, 35 N-butanol, isobutanol, secondary butanol and t. N. Also monoesters of ethylene glycol, diethylene glycol, polyethylene glycol, propylene glycol, e.g. monsmetilovy ether, ethylene glycol monoetilszhogo ethylene glycol ether, mono-butyl ether of ethylene glycol, monoethyl ether of diethylene glycol, mono-ethyl ether of propylene glycol, etc.
    As component II, reoolcarboxylic acids obtained by known methods of condensation of formaldehyde with phenolcarboxylic acids, such as 2- (4-hydroxyphenyl) -2- (carboethoxyfephenyl) -propyl or 4, 4-6c- ( 4-hydroxyphenyl) -valeric acid, under known conditions, after partial or complete esterification. methylol groups.
    The condensation products of formaldehyde with phenols, such as m-tert-butylphenol, 2,2-iS Mc- (4-hydroxyphenyl) propane or urea, thiourea, melamine, can also be used. benzoguanamine and others under known conditions, after esterification of CAO with lower alcohols. When using aminoplast components, drying temperatures can be reduced.
    Suitable compounds for polyhydroxy compounds are co-65.
    At drying temperatures used for the film-forming substances described in this invention, they are so low-volatile that they contribute to the creation of a hardened film-forming substance. Organic compounds include: ethylene glycol, propylene glycol, butylene glycol neopentyl glycol, glycerin, trimethyl propane, pentaerythritol, derivatives of diphenylol propane esters with epichlorohydrin without epoxy groups, for example, partial fatty acid esters, further amino alcohols, such as triethanolamine, as well as epoxy groups, and epoxy groups; tetrakis-2-hydrospropylethylenediamine, then polymers containing hydroxyl groups, which, for example, are obtained by polymerizing ally alcohol or monoethylene glycol ester of (meth) acrylic acid , under known conditions, with other L, monosaturated with two bonds (such as styrene, vinyl toluene, esters of (meth) acrylic acid, vinyl acetate, (meth) acrylamide, (methacrylonitrile) or by reacting ethylene oxide with freshly prepared carboxyl groups to polymers. In addition, products with special properties are obtained if polyhydroxy compounds are partially replaced by isocyanates, so that at least two hydroxyl groups remain in the final product
    The following bases are suitable for neutralizing the invented products: in addition to ammonia, primary, secondary, tertiary alkylamine, for example (iso) propylamine, butylamine, amylamine, diethylamine, diisopropylamine, diiaobutylamine, morpholine, Pineridine, trimethylamine, triethylamine, and alkanolim, morpholine, Pineridine, trimethylamine, triethylamine, and alkanolim, morpholine, Pineridine, trimethylamine, triethylamine, and alkanalamines, i-nam, amiminomine, triethylamine, as well as alcanols, which are also the numbers for which I and , and alkylene polysin1, for example, ethylene diamine, diethylenetriamine, triethylene tetramine, etc.
    When using the proposed co-bruising agents to neutralize electrophoretic varnishes, alkaline and / or alkaline-earth oxide hydrates and acid salts can also be used, whose dissociation constant is lower than that of the proposed synthetic resin, since they are, under known conditions in the presence of co-containing solvents, form water-soluble soaps.
    Examples of corresponding salts of weakly dissociated acids are alkali carbonates, alkaline carbamates, etc.
    In order to maintain solubility in the cave and to better utilize the resin, the film-forming substances invented may also contain solvents. The following solvents can be mixed indefinitely with water: methaNOL, ethanol, (iso) propanol, sec-6-butanol ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol mononopropyl ether, diacetone alcohol, dimethylformamide, etc. In fewer quantities, ethylene glycol monoethyl ether, diacetone alcohol, dimethylformamide and others. Water soluble solvents can also be used as a binder. Under these solvents are higher alcohols, such as n-butanol, (iso) octanol, (iso) tridecanol, higher glycol esters, such as n-butyl glycolic esters, diethylene glycol monobutyl ether, aliphatic, hydroaromatic or aromatic hydrocarbons, such as gasoline fractions, tetrahydronaphthalene, decahydronaphthalene, benzene, toluene, xylene, ethylenebenzene, etc. Higher ketones, such as trimethylcyclohexanone (isophorone), etc.
    The proposed film-forming substances can be applied in pigmented or non-pigmented form by all known methods.
    When deposited by anthrax deposition, deposited films provide good anti-corrosion protection of metals when tested in a salt cloud and in an industrial atmosphere. It is particularly important that coating films of the invented film-forming substances provide good protection for steel surfaces that are not subjected to pre-treatment. Thus, during the mass production of lacquered metal objects, it is possible to eliminate the unpleasant processes of phosphatization and chromatising.
    In contrast to the film-forming substances, the proposed ones have an increased resistance of the solutions to oxidation, and give a more uniform varnish coating for a longer period.
    Production instructions for component I.
    1.400 g of polybutadiene having a viscosity of 5 P (20 ° C), containing about 80% of the cis - and 20% trans isomers and having a molecular weight of 1400 g, together with 1.5 g of copper naphthenate, containing 9% of metal and 100 g maleic anhydride, heated to 200 ° C. After 2.5 h, the content in the reaction mixture of maleic anhydride drops to 0. The acid number of the reaction product is 190 mg KOH / g. The mixture is cooled to 100 ° C, 50 g of diacetone alcohol are added and 35 g of methanol are gradually added under reflux. Maintain a temperature of 90100 ° C, while the acid number decreases
    up to 90-95 mg KOH / H ..
    2,500 g of polybutadiene having a viscosity of 9 P (45 ° C), isomeric composition
    80% 1,2-vinyl and 20% tpoHC forms and molecular weight 1200, together with 0.1 g diphenyl-p-phenylenediamine and 100 g maleic anhydride, are heated to 200 ° C until the content of free maleic anhydride is reduced to zero. Cool until. Acid number 160 mg KOH / g. Add 90 g ethylene glycol monomethyl ether mixed with 3 g triethylamine and maintain the temperature at 140 until the acid number drops to 65 mg KOH / g.
    3. 400 g of polybutadiene having a viscosity of 5 P (20 s), an isomeric composition of 80%, 1,4-TsIS- and 20% 1,4-trans structure and molecular, are heated in an inert gas atmosphere to. A solution consisting of 0.6 g of di-tert-butyl peroxide in 60 g of vinyl toluene is added evenly over 2 hours and the temperature is maintained at 150 ° C until at least 95% of the solid is formed.
    Unreacted vinyl toluene is removed in vacuo and a graft copolymer with a viscosity of 13 P (20 ° C) is obtained.
    400 g of this material, together with 0.1 g of diphenyl-p-phenylenediamine and 100 g of maleic anhydride, are heated to 200 ° C. After 3 hours of reaction, the content of maleic acid free anhydride decreases to zero. A product with an acid number of 190 mg KOH / g and a viscosity of 1 P (Gardner-Holt) measured in a solution consisting of 60 g of resin and 40 g of ethylene glycol monoethyl ether acetate is obtained.
    After cooling, a solution of 1GO of ethylene glycol monoethyl ether and 3 g of N, N-dimethylbenzylamine is added. Acid number after the last reaction 90 mg KOH / g.
    Production instructions for component II.
    1.360 g of a 36% formaldehyde solution, 106 g of triethylamine and 286 g of H, 4-bis- (4-hydroxyphenyl) -valerian, its acid is heated up to the pH of the reaction mixture (measured 1:10 in distilled water) with further the addition of triethylamine is established. 7.7-8.0.
    Hold 10h at 80 ° C and cool.
    2.288 g of 2,2-6-sis- (4-hydroxyphenyl) propane are dissolved in 500 ml of 2 sodium alkali when heated. Then, a solution of 110 g of sodium salt of chloroacetic acid (technical.) In 170 g of water is mixed in, the temperature is gradually changed to 60–90 ° C and the mixture is constantly stirred for 1 hour.
    权利要求:
    Claims (1)
    [1]
    The reaction mass is combined with 200 g of formaldehyde (35% solution) to form a clear solution, and is kept for 3 days at 40 ° C. Then, in the presence of 100 g of butanol and the calculated amount of hydrochloric acid, rezolcaric acid and resole are precipitated. After repeated washing, 500 g of butanol solution are obtained, with an acid number of 140 mg KOH / g on average. The content of the solid substance is 65%. After the solution has been neutralized with ammonia, it is infinitely diluted with water. 3. An excess, in excess of the theoretical amount, of the sodium salt of chloroacetic acid is used, which favors practically quantitative esterification of the phenolic hydroxyl group and in this way obtaining a significant amount of diphenylol glycol ether or sodium salt. Then, as described in paragraph 2, it is condensed with 175 g of formaldehyde and finally processed with 114 g of butane ol or Cyclohexanol. The condensate has an acid value of an average of 155 mg KOH / H. Instead of 2.2-6is - (4-hydroxyphenyl) -propane, other analogous bisphenols derived from higher ketones, such as methyl ethyl ketone cyclohexanone, methylene cyclohexanone, etc., can be used. Instead of alkane radical, a bridge in bisphenol can form so, or as bisphocion or la can serve directly dioxydiphenyl. 4. To a mixture of 180 g of formaldegnd 36% and 3 g of 40% sodium alkali, 150 g of p-tert-butylphenol are continuously added over 1 hour, then another 12 g of 40% sodium is added over 6 hours. alkali. After 48 hours at 40 ° C, a transparent solution was formed containing 2% free formal sugar. 50 g of secondary butanol and 100 g of 40% sodium alkali, etc., are added at 50 ° C, according to the exothermic: reaction, 120 g of sodium salt of chloroacetic acid. The mixture was kept for 5 hours at a temperature of 80 ° C. The precipitate of carboxylic acid was extracted with 103 r of 50% sulfuric acid and washed several times with water. The solids content is about 70%, the acid number is about 140 mg KOH / g. The following examples clarify the invention, but without limiting it. Example 1. 58 5 g of compo nent I (p. I) 200 g of ethylene glycol monoethyl efl and 60 g of copolymerization consisting of allyl alcohol and styrene with a hydroxyl equivalent of 300 U mol. 1600, with stirring, heated to 110 ° C. This temperature is maintained until a sample of the reaction mixture, after neutralization with ammonia, gives a clear solution with water. It is cooled to (eO-C and 200 g of component II is added. Acid number is 90-100 mg KOH / g. 70 ml of concentrated ammonia is added with stirring at the room temperature. Neutralized resin has 70% solids. 290 g of this neutralized binder the substances are ground on a three-roll machine together with 20 g of TiOg (rutile), 20 g of red iron oxide pigment (redoxide) and 20 g of aluminum silicate. This varnish paste is diluted with 1600 g of deionized water and pH is 7.5 with further ammonia. metallic A 2.5-liter vessel connected as a cathode on an anode with a surface of 200 cm from a phosphated steel sheet from a varnish solution at 2 for 1 min at 100 V DC a dense, well-rinsing layer is deposited. After curing for 30 min at 180 s a 28 µm tolcina coating was formed.After 240 hours of testing, according to the ASTM instructions, 3 mm of corrosion was found on the cross-shaped scratch of the metal sample. The varnish solution is stirred for 200 hours at 40 ° C and then cooled to 25 ° C. The deposited deposition is repeated and an immaculate coating is obtained with the same corrosion effect. Example 2. 690 g of component II (p. 2) 200 g of ethylene glycol monobutyl ether and 100 g of diethoxydiphenylol propane are heated to and kept at this temperature until the sample of the mixture after neutralization with triethylamine forms a clear solution in water. 100 g of component II (p. 2) is added and diluted with ethylene glycol monobutyl ether to a content of 70% solid veutecTBa, the resin is diluted with triethylamine and water to a 25% solution with a pH of 7, 8. This solution is applied using rollers on a large moving steel strip, after 10 seconds of curing it forms a highly elastic, solid, corrosion resistant film with a thickness of 5 microns. Example 3 600 g of component 1 (p. 3) are mixed with 200 g of component B (p. 3), then 60 g of isoferone are added and the reaction mixture is diluted with isopropanol to 70% solids . The resin solution is treated with an amount of 40% potassium hydroxide solution so that an aqueous solution with a 10% resin content has a pH of 7.5. 330 g of this neutralized solution in a suspending agent on a three-roll machine rolls with 32 g of TiO (rutile), 32 g of aluminum silicate and 2 g of carbon black. After the addition of 1600 g of water, a solution of varnish is obtained, further processed as described in ia of Example 1. The films obtained are 25 µm thick. After 240 hours of testing in salt mist according to ASTM 117-61 on a cross-shaped scratch of a 2 mm corrosion test plate. After 200 hours of stirring at 40 ° C, immaculate coatings with good corrosion protection are also obtained from this lacquer solution. To test the setting (Throwi Power), the lacquer solution is poured into a plastic cylinder with a diameter of b cm and a capacity of 1 liter, having a cathode in the form of a washer of the same diameter at the bottom. As an anode, a metal strip 5 cm wide is immersed in the test material. The end of the strip is 2 cm away from the cathode. One minute after applying a layer at 200 V by rinsing with deionized water and 30 minutes of curing at the bottom of the strip, the measured thickness of the coating is 26 Mkm. parts of the strip. (at the boundary of immersion) - thickness of the coating is 15 µm. Compared to the main patent, where the coating thickness of the upper end of the strip is only 4 µm, the example -3 given compares favorably. PRI me R 4. 585 g of component I (p. 1) is well mixed with 65 g of component (p. 4) and 240 g of ethylene glycol monoethyl ether at room temperature. The resulting resin solution contains 65% solids. After neutralization with ammonia to a pH of 7.0 (measured in 10% solution of distilled water, the resin is pigmented as in Example 1, dissolves and is deposited anodically. The test according to Example 3 of the steel plate and the measurements showed the thickness of the film layer in the lower part of the plate 20 µm and in the upper part - 14 m. Covered with a 28 µm layer, the dried phosphated steel plate after 240 hours of testing in a salt chamber according to ASTM B 117-61 instructions, on a cross-shaped scratch, gives a corrosion depth of 2 mm. The primary composition comprising the product (I) of reacting a diene polymer with an el, p-unsaturated carboxylic acid or dicarboxylic acid or its anhydride, or a polyester or semi-amide, the product II is a tar-reactive phenol-formaldehyde resin, obtained by condensing a formaldehyde acid with a phenol carboxylic acid or a polymerase or a phenol-formaldehyde resin, obtained by condensation of a formaldehyde with a phenol carboxylic acid or a phenol or phenol formaldehyde resin, obtained by condensing formaldehyde with a phenol carboxylic acid or a phenol-formaldehyde resin, obtained by condensation of a formaldehyde with a phenol carboxylic acid or a phenol or phenol formaldehyde resin, obtained by condensing formaldehyde with a phenol carboxylic acid or a phenol-formaldehyde resin, obtained by condensation of a formaldehyde with a phenolcarboxylic acid or a phenol or phenol formaldehyde resin; a solvent, characterized in that, in order to increase the corrosion resistance of the coating, as product I it contains the product of the interaction of a diene polymer with (X, p) non-saturated carboxylic acid, or dicarboxylic acid, or its anhydride, or half-rum, or semi-amide, containing 50-70% of esterified carboxyl groups, with a ratio of products I and II, calculated on dry matter,%: Product I70-95 Product II30-5 Information sources, tie into account during the examination 1. USSR Patent No. 305666, l. C 09 D 3/48, 1969 (prototype).
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    同族专利:
    公开号 | 公开日
    CH561269A5|1975-04-30|
    BE767776R|1971-10-18|
    DE2120962B2|1976-05-20|
    NO134163C|1976-08-25|
    SE380284B|1975-11-03|
    PL88912B3|1976-10-30|
    RO59429A7|1976-02-15|
    US3796770A|1974-03-12|
    IT983135B|1974-10-31|
    ES391931A2|1973-08-01|
    CA991338A|1976-06-15|
    BG20388A3|1975-11-05|
    CS183651B2|1978-07-31|
    JPS5328460B1|1978-08-15|
    HU163652B|1973-09-27|
    ZA712674B|1972-01-26|
    GB1330992A|1973-09-19|
    NO134163B|1976-05-18|
    DE2120962A1|1972-01-27|
    引用文献:
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    CA976290A|1972-12-29|1975-10-14|Canada Wire And Cable Limited|Process and bath composition for increasing the rate of polymer deposition in electrocoating|
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    US4025473A|1975-03-26|1977-05-24|Union Carbide Corporation|Process for producing water-dilutable coating compositions|
    AT350157B|1976-08-20|1979-05-10|Herberts & Co Gmbh|Aqueous, phenolic resin-free coating agent and process for its manufacture|
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    JPH0318093A|1989-06-15|1991-01-25|Matsushita Electric Works Ltd|Cleaning device for wiring board|
    AT407253B|1997-10-06|2001-02-26|Vianova Kunstharz Ag|WATER-THINNABLE RESINS, METHOD FOR THEIR PRODUCTION AND THEIR USE|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    AT666770A|AT303920B|1970-07-22|1970-07-22|Aqueous coating agent|
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