Method of preparing water soluble binder for hot-setting lacquers

专利摘要:

公开号:SU1748650A3
申请号:SU874203919
申请日:1987-12-22
公开日:1992-07-15
发明作者:Штаритцбихлер Вернер；Дворак Герт；Даймер Вольфганг
申请人:Вианова Кунстхарц, Аг (Фирма)；
IPC主号:

专利说明:

PRI me R 1, Component (1/1). In a suitable reaction vessel, a mixture of 165 parts by weight is subjected to transesterification. dehydrated castor oil and 135 wt.h. linseed oil for 1 h at 250 ° C. After cooling to 170 ° C, 100 wt.h. maleic anhydride and perform the reaction at 210 ° C until more unbound maleic acid is detected. The resulting adduct is cooled to 90 ° C and after adding a mixture of 30 wt.h. water and 3 wt.h, triethylamine is subjected to hydrolysis. Then, the initial mixture is diluted with methoxypropanol to a solid content of 80%. The resin has a viscosity limit (dimethylformamide at 20 ° C) of 6.5 ± 0.3 ml / g, acid number 268 mgKOH / g,
Component (11/1).
475 parts by weight Epoxy resin (epoxy equivalent weight EEV - about 475 ± 25) is dissolved in 100 wt.h. diethylene glycol dimethyl ether. At 80 ° C, a mixture of 105 parts by weight, diztanolamine and 45 parts by weight is added. dimethyl ether diethylene glycol and carry out the reaction almost to complete conversion. Then, in the initial mixture with the help of methyl ethyl ketone, the solids content is 65% and the addition of parts of about 40 wt.h. toluene diisocyanate increases the viscosity limit (measured in dimethylformamide at 20 ° C) to 10 ± 0.3 ml / g, the hydroxyl number 230 mg COH / g, the solvent is distilled off in vacuo to a solids content of 8%.
The binder is prepared as follows.
25 wt.h. component (1/1) and 100 wt.h. component (11/1) are mixed (mass ratio of 20:80). Partial condensation occurs at approximately 100 ° C until the limiting viscosity number (measured in dimethylformamide at 20 ° C) reaches 16 ± Of 3 ml / g. After cooling, the initial mixture is neutralized with 6 wt.h. dimethylethanolamine and diluted with deionized water to a solids content of 35%.
Example 2. Component (I / 2) was prepared according to example 1 out of 80 wt.h. dehydrated castor oil, 100 wt.h. linseed oil, 70 May, h, soybean oil and 100 wt.h. maleic anhydride. In this case, the anhydride groups are cleaved using the amount of methanol needed to form the half-ester after the addition of a catalytic amount of triethylamine. The initial mixture is diluted with methoxypropanol to a solids content of 80%. The resin has a viscosity limit (dimethylformamide at
20 ° C) 5.5 ± 0.3 ml / g, acid number 146 mgKOH / g.
Component (And / 2) receive, dissolving 925 wt.h. epoxy resin (EEV 925 ± 50) 250 wt.h. dimethyl ether
diethylene glycol, at 80 ° C. The mixture was added from May 133, hours. diisopropanolamine and 100 wt.h. diethylene glycol dimethyl ether and reacted until complete conversion. Initial mixture
with methyl ethyl ketone, it is adjusted to a solids content of 65%. By adding parts of about 35 wt.h. and hexamethylenediisocyanate increases the viscosity limit of 20 ° C to 10.2 ± 0.3 ml / g;
the hydroxyl number is 130 mgKOH / g. The solvent is distilled off in vacuo to a solids content of 80%.
The binder is prepared as follows.
37.5 wt.h. 80% solution of the component (/ 2) and 87.5 wt.h. The 80% solution of the component (I / 2) is condensed at 110 ° С (mass ratio 30:70), while the limiting viscosity number (dimethylformamide
at 20 ° C) does not reach 14.2 ± 0.3 ml / g, the initial mixture is neutralized after cooling on 5 May, including diethanolamine and diluted with deionized water to a solids content of 35%,
PRI me R 3. Component (I / 3) is prepared according to Example 1 out of 250 parts by weight. dehydrated castor oil, 100 wt.h. linseed oil and 100 wt.h. maleic anhydride. Anhydrite groups are cleaved with the help of May 30, h, water in the presence of 3 wt.h. triethylamine. The initial mixture is diluted with methoxypropanol to a solid content of 80%. The resin has a viscosity limit of 6.0 ± 0.3 dimethylformamide
ml / g, acid number 239 mgKOH / g.
Component (I / 3) ready to dissolve 237 wt.h. Epoxy resin EEV 475 ± 25 and 462 wt.h. Epoxy resin EEV 925 ± 50 200 wt.h, dimethyl ether
diethylene glycol. At 80 ° C, a mixture of 105 parts by weight is added to the solution. diethanolamines and 100 May, h, diethylene glycol dimethyl ether and carried out the reaction until complete conversion. The original mixture using
5 methyl ethyl ketone is adjusted to a solids content of 65%. By adding parts about 40 May, h. toluene diisocyanate increase the viscosity limit hydroxyl number 168 mgKOH / g to
11.8 ± 0.3 ml / g; the solvent is distilled off in vacuo to a solid content of 80%.
The binder is obtained by subjecting condensation at 120 ° С to 31.25 wt.h of the 80% solution of the component (/ 3) and 93.75 wt.h. 80% solution of the component (M / 3), mass ratio 25:75, while the maximum viscosity number does not reach 15.2 ± 0.3 ml / g. After cooling, the initial mixture is neutralized with 6 mph. dimethylethanolamine and diluted with deionized water to a solids content of 35%
EXAMPLE 4. Component (I / 4) is identical to component (1/1).
Component (And / 4) was obtained as follows.
In the corresponding reaction vessel 150 wt.h. triethylene glycol, 134 mph. trimethylolpropane and 148 wt.h. phthalic anhydride is brought to 220 ° C and esterified at this temperature until the acid number reaches about 3 mg KOH / g, the viscosity of DIN 53 211/20 ° C (70% in butyl glycol) is 75-125 seconds The resulting hydroxyl-containing polyester. To a mixture of 105 wt.h diethanolamine, 116 wt.h. the obtained polyester and 74 wt.h. diethylene glycol dimethyl ether was added in portions at 80 ° C to 594 parts by weight. a solution consisting of 475 wt.h. epoxy - dian resin EEV 475 ± 20 and 119 wt.h. dimethyl ether diethylene glycol. The reaction is carried out until complete conversion of the oxirane groups. Then 75 parts by weight of mono-epoxy compound (tertiary Cd-Mono-carboxylic acid glycidyl ester) is added.
The temperature is raised to 160 ° C and maintained until more unrelated epoxy groups are detected,
At 70 ° C, a solid content of 66% is established in the initial mixture using methyl ethyl ketone and by adding portions to about 45 wt.h. toluene diisocyanate exceeds the viscosity limit to a value of about 10.3 ± 0.3 ml / g, a hydroxyl number 280 mg COH / g. The solvent is distilled off in vacuum to a solid content of 80%.
Binder is prepared as follows.
Mix 25 wt.h. component (1/1) and 100 wt.h. component (P / 4) mass ratio of 20:80. Partial condensation occurs at approximately 105 ° C until the limiting viscosity number reaches about 17 ± 0.3 mg / g. After cooling to 90 ° C, the initial mixture is neutralized with 6 parts by weight. dimethylethanolamine and diluted with deionized water to containing and solid matter 35%.
In a known manner, pigment-like pigments are obtained on a bead 5 mill, which are lacquered with an appropriate binder and mixed with melamine formaldehyde resin.
Lacquer formulation, wt.h / 0 Binder solution
35% in Example 1-4 123 Deionized water25
Titanium dioxide
5 (Rutile) 80
Barium sulphate 40
Flame Soot0,2
Pasta268.2
Binder Solution 0 35% in Example 1-4.193 Hexamethoxymethylmelamine 100% 12 Lac 473.2 5 The solids content is about 51-52%, pH 9.0, spreading time according to DIN 53 211/20 ° About 30 s
Pigmented standard varnish with 0 resin by a known method.
Pigment in the form of a paste is obtained from 57.4 wt.h 75% binder, 37.8 wt.h. ethylene glycol monobutyl ether, 80 wt.h. titanium dioxide (Rutile type), 40 5 wt.h. barium sulfate and 0.2 wt.h. soot flame; Paste in the form of varnish is made up of 90.1 wt.h. resin 75%, 12 wt.h. hexa-methoxyethylmelamine (100%), 17.5 wt.h. ethylene glycol monobutyl ether 0 and 14 wt.h. deionized water.
A binder according to a known method is prepared as follows.
Component (I / 5): 156 g of dihydrated castor oil and 78 g of flax 5 oil are stirred for 1 hour at 250 ° C in an inert gas atmosphere. At 200 ° C, 100 g of maleic anhydride is added. After about 30 seconds of reaction at 210 ° C, unbound ana-0 maleic acid hydride is no longer detected. At 100 ° C, 70 g of diacetone alcohol, 30 g of water and 2 g of triethylamine are added. Stand 2 hours at 100 ° C and then cool. The resin has a solids content of 85% and an acid value of 250 mgKOH / g.
Component (11/5): 150 g of triethylene glycol and 148 g of phthalic anhydride are heated in a reaction vessel with a stirrer, a water separator and incubated to those
until the acid number reaches 188 mgKOH / r, 134 g of trimethylolpropane is added and esterified at 220 ° C to an acid number of less than 5 kg KOH / r, about 27 g of the reaction water are distilled off, the resin is cooled and it is ready for for use, the spreading time of a 70% aqueous solution of resin in ethylene glycol monobutyl ether over DIN 53 211 is about 80 seconds.
A known binder is prepared as follows. In a reaction vessel with a stirrer and reflux condenser, 36 g of polycarboxylic component (I / 5) and 70 g of polyhydroxyl component (H / 5) are heated together to 120 ° C and condensed to about 1 hour to an acid number, which is first 76 and 68 mgKOH / g, and viscosity limit 14.3 ± 0.3 ml / g. 14 g of ethylene glycol monobutyl ether and 9 g of secondary butanol are diluted. To neutralize the initial mixture is mixed with 6 mph. dimethyl ethane; Lamin.
The results of technical testing varnish.
The varnishes are sprayed onto untreated steel sheet and dried by hot drying at 120; 140 and 160 ° C. The films have a dry film thickness of 25 to 30 mm.
Coating properties are listed in the table.

权利要求:
Claims (1)
[1]
Invention Formula
The method of producing a water-soluble binder for hot-drying varnishes by reacting polycarboxylic and polyhydroxylic components at 100-120 ° C, characterized in that
the purpose of increasing the salt resistance and tropical stability of coatings based on a binder, as the polycarboxylic component, the product of the interaction 100 wt.h. maleic anhydride and 250-350 wt.h. dehydrated castor and flax oils or their mixture with soybean oil with an acid number of 146– 268 mgKOH / g, with a viscosity value after
treatment with water or its mixture with methanol, measured in dimethylformamide at 20 ° C, 5.2-6.8 ml / g, as a polyhydroxy component use the product of the interaction of diethanolamine, an epoxy-diane resin with an epoxy equivalent of 450-975 and toluene diisocyanate or the product of interaction diisopropanolamine, 450-975 epoxy resin with epoxy equivalent and hexamethylene diisocyanate, or the product of diethanolamine, 475 ± 20 epoxy resin, epoxy resin, trimethyl polyether propane and phthalic anhydride with
acid number 3 mgKOH / g, glycidyl ether of tertiary Cd-Sp-mono carboxylic acid and toluene diisocyanate with viscosity value of the reaction product, measured in dimethylformamide at
20 ° C, 9.7-12.1 ml / g and a hydroxyl number of 130-280 mgKOH / g, with the mass ratio of the polycarboxyl and polyhydroxyl components being (20-30}; (70-80), respectively, and the interaction of the components to obtain a product with viscosity values measured in dimethylformamide at 20 ° C, 13.9-17.3 ml / g.

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法律状态:

优先权:

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