Plaste-forming resin for universal pigment paste

FIELD: chemistry.

SUBSTANCE: paste-forming resin AB which is a mixture of a water-reducible alkyd resin B and a basic acrylic copolymer resin A, wherein the basic acrylic copolymer resin A is a copolymer of at least three classes of vinyl monomers having each at least one copolymerisable olefinic unsaturation, the vinyl monomers comprising at least one amino group-containing vinyl type monomer Al, at least one monomer A2 selected from a group consisting of linear or branched alkyl(meth)acrylates having from 1 to 13 carbon atoms in the alkyl group, and at least one hydrophilic vinyl monomer A3 having a moiety derived from a polyether glycol which is a polyethylene glycol or a mixed ether of ethylene and propylene glycol having a weight ratio of at least 60% of oxyethylene groups in the total mass of oxyalkylene groups, where one of the hydroxyl groups of the polyether glycol is converted to an ether group, and the other hydroxyl group is removed by esterification with an olefinically unsaturated monocarboxylic acid, or by etherification with an olefinically unsaturated alcohol, or by urethane formation via reaction with an adduct of a hydroxyalkyl(meth)acrylate and a diisocyanate. The pigment paste contains a paste-forming resin AB and at least one pigment selected from a group comprising inorganic pigments and organic pigments. The method of applying the paste-forming resin involves mixing said paste-forming resin AB with at least one pigment, homogenisation of the mixture with a shearing force to obtain a pigment paste and mixing said pigment paste with a non-pigmented or white pigmented dye which contains an organic binder for dye.

EFFECT: obtaining a pigment paste which contains a pigment-forming resin which is compatible with most types of pigments and binding resins.

12 cl, 4 tbl, 7 ex

 

The technical FIELD

The present invention relates to a paste resin for universal pigment paste for kolorowania color paints.

The LEVEL of TECHNOLOGY

In the paint and coatings industry, raw material control and procurement carried out through the use of systems of color mixing. In such systems, paint color selected by the user, is obtained by selecting a base paint from a number of available base colors and add to the selected base paint one or more pigment pastes, which are homogeneous mixtures of one or more pigments with paste resins, the latter have good dispersing properties. Such systems are widely used in the field of decorative coatings, as disclosed, for example, in the publication EP 0311209 A1.

Examples of pigment paste for tinting paints disclosed in the publications WO 91/06607 A1 (polyesters, water-based), WO 99/49963 A1 (polyether oil-based) and EP 0458479 A2 (modified acrylic polyol for paints oil-based). In addition, at least one pigment pigment pastes typically include special resins, solvents and also, typically, additives. Pigments for different colors vary in their chemical nature from simple inorganic elements,such as carbon in the form of a gas channel carbon black or lamp black, to inorganic oxides (such as iron oxide, pigments based on copper, cobalt, chromium and lead) and organic pigments (such as azo pigments, phthalocyanine pigments and polycyclic aromatic pigments such as Pereladova, antrahinonove and chinaredorbit pigments). For each pigment, you must use a compatible resin. This resin, in turn, must be compatible with the binder system of basic paints and resins used in other pigment pastes, because most of the colors you want to add more than one pigment paste. The resin must also be capable of dispersing a sufficient amount of pigment. Up to now, no you can't use system kolorowania compatible with paints oil-based and water-based paints, and which is also compatible with the usual assortment of binder resins.

The INVENTION

Thus, the objective of the present invention to provide pigment paste containing a resin ("paste resin"), which is compatible with most types of pigments, as well as with most of the resins, whether they are oil-based or water-based. Paste resin must have sufficient dispersing and wetting ability to atomized R is neobreznye pigments based on various raw materials, for example, the materials mentioned above.

The purpose of the invention is achieved through the development of paste resin which is a mixture with water-dilutable alkyd resin and acrylic base copolymer resin A, where the base acrylic copolymer resin A is a copolymer of at least three classes of vinyl monomers, each of which has at least one capable of copolymerization of olefinic unsaturation, and vinyl monomers contain at least one vinyl monomer of type A1 containing the amino group, at least one monomer A2 selected from the group including linear or branched alkyl(meth)acrylates, containing from 1 to 13 carbon atoms in the alkyl group, and at least one hydrophilic vinyl monomer A3 containing the residue obtained from polifonicos, which is a polyethylene glycol or a mixed ether of ethylene - and propylene glycol having a mass fraction of at least 60% oxyethylene groups in the total mass oxyalkylene groups, where one of the hydroxyl groups of polifonicos converted to simple ester group and the other hydroxyl group is removed by esterification with refinancing monocarboxylic acid or by etherification with refinancing alcohol, or by the formation of urethane on R. the action with the adduct hydroxyalkyl(meth)acrylate and diisocyanate.

A DETAILED DESCRIPTION of the PREFERRED embodiments

With water-dilutable alkyd resin preferably has an acid number of from 0.2 to 5 mg/g, particularly preferably from 0.5 to 3 mg/g, and preferably dynamic viscosity, measured at 50% concentration dispersion in water at a temperature of 23ºC and shear stress 25 sec-1in accordance with DIN EN ISO 3219, from 5 to 25 MPa·s.

Alkyd resin-based condensation product of an alkyd resin BA and adduct Bb C1-C4-monoalkyl ether Bb1 of polyoxyethyleneglycol or C1-C4-monoalkyl ether Bb2 simple mixed ether of ethylene - and propylene glycol, or mixtures thereof, and anhydride Bb3 cycloaliphatic carboxylic acids, and the ratio of the sum of the quantities of substances Bb1 and Bb2 to the amount of matter B3 is preferably from 0.95:1.05 of the mol. to 1.05: 0.95 to say.

With water-dilutable alkyd resin is preferably obtained by reaction of BA and Bb in the conditions of the esterification reaction, i.e. removal of water, preferably in the presence of the arresting agent such as xylene, by azeotropic distillation and recycling of the arresting agent. It is also possible to use conventional esterification catalysts. The esterification at a temperature of preferably from 170 to 260º hold up until the selected sample will not have the acid number of 3 mg/g or lower.

In U.S. patent 3878140 covering disclosed a composition comprising a mixture of (A) a mixture of acrylic copolymer (A1)derived from a methacrylate and alkylacrylate or alkylmethacrylamide, each of which contains from 2 to 12 carbon atoms in the alkyl group, the second acrylic copolymer (A2)derived from a methacrylate and monomer, stimulating adhesion, such as 3-(2-methacryloxyethyl)-2,2-Spiro-cyclohexylacetate, and the plasticizer (A3), which is either an ester of phthalic acid, or alkyd resins, and pigmented acrylic composition (B)containing the copolymer (B1), which is a polymethyl methacrylate or a copolymer of methyl methacrylate or a mixture of these polymers, and acetobutyrate cellulose (B2) and an organic plasticizer (B3). The plasticizer alkyd resin, disclosed herein, is a reaction product is non-drying fatty acid, a polyhydric alcohol and a dicarboxylic acid or its anhydride.

Antifouling agent, known from the published patent application U.S. 2005/00964075 A1, is a combination of biocidal active substances and non-aqueous dispersion of a polymeric binder containing as a dispersing medium for the polymerization of acrylic resin, at least one alkyd resin, having a Mac is UNIX share of non-volatile material, at least 90%, z-average molecular weight of between 10 and 250 kg/mol, with a mass ratio of alkyd parts acrylic pieces from 50:50 to 30:70. Used alkyd resin may be a fatty Alcide or Alcide medium oil-based fatty acid soybean or linseed oil, which is also confirmed by the example 1A (soybean oil, trimellitic anhydride and trimethylated) and 1B (fatty acid of soybean oil, pentaerythritol, CROTONALDEHYDE and isophthalic acid).

The acid number is determined, as is customary in accordance with DIN EN ISO 3682, as the ratio of the mass m (KOH) potassium hydroxide required to neutralize the sample with a mass m (sample), for a given mass m (sample); in the case of a solution or dispersion in sample m (sample) replace weight solids m (solids) in the specified solution or dispersion, and adopted by the measurement unit is "mg/g".

Alkyd resin BA usually obtained by deposition of one or more polyols Ba1 having in the molecule two or more hydroxyl groups, one or more polybasic acids (which have in the molecule two or more acid groups) Ba2 and one or more fatty acids Ba3, which can be substituted or mixed with one or more triglyceride oils VA. Optionally the reaction mixture to which hensachi may also contain one or more monobasic acids WA. Preferably, at least one of the fatty acids Ba3 contains in the molecule at least one olefinic unsaturation. Preferably, at least one of triglyceride oils V contains at least one residue formed from fatty acids having in the molecule at least one olefinic unsaturation.

The polyols Ba1 are aliphatic linear or branched hydroxyl compounds containing in the molecule from two to six hydroxyl groups, preferably up to four hydroxyl groups in the molecule, such as ethylene glycol, 1,2 - and 1,3-propylene glycol, 1,2 - and 1,4-butanediol, glycerin, trimethylolpropane, trimethylacetyl, aritra, threitol, pentaerythritol, ditrimethylol, ditrimethylol, sorbitol and beckoning.

Polybasic acid Ba2 can be aliphatic linear, branched or cyclic, or aromatic, containing from two to four acid groups, and preferably from 3 to 20 carbon atoms, and preferably may be selected from the group comprising phthalic acid, trimellitic acid, tetrahydrophthalic acid, adipic acid, malonic acid, cyclohexanecarbonyl acid, isophthalic and terephthalic acid, and benzophenonetetracarboxylic acid.

Fatty acids Ba3 preferably represent from the fight, at least mooreindonesia aliphatic monocarboxylic acid, preferably containing from 4 to 24 carbon atoms. Preferred acids are lauric, Mirandolina, palmitoleic, oleic, gadolinia, erucic, ricinoleic, linoleic and linolenic acids, and their mixtures, especially existing in the nature of the mixture, such as fatty acid, soybean oil fatty acid, linseed oil fatty acid, sunflower oil fatty acid, safflower oil fatty acid seed oil rubber and tall oil fatty acid.

Triglyceride oils We represent oil, preferably having an iodine number of from 120 to 200 IG/g (centigram/g), particularly preferably soybean oil, linseed oil, sunflower oil, safflower oil, seed oil, rubber and tall oil.

Monobasic acid We preferably are aromatic monobasic acids such as benzoic acid or alkyl substituted benzoic acid, cycloaliphatic monobasic acids, especially those in the so-called resin acids, branched aliphatic carboxylic acids, such as isononanoic acid, 2-ethylhexanoate acid or acid "Versatic"®the mixture of alpha-branched dejanovich acids.

Preferably alkyd with the Ola VA have an acid number less than 5 mg/g, particularly preferably from 0.1 to 4 mg/g and most preferably from 0.2 to 3.5 mg/year of Their hydroxyl number is preferably from 30 to 100 mg/g, particularly preferably from 40 to 90 mg/g and most preferably from 60 to 85 mg/g

Adduct Bb is a reaction product containing a hydroxyl group monoalkyl ether Bb1 selected from the group comprising From1-C4-monoalkyl esters of Bb11 polyoxyethyleneglycol,1-C4-monoalkyl ether Bb12 mixed ether of ethylene and propylene glycol and mixtures thereof, and anhydride Bb2 cycloaliphatic dicarboxylic acids, and the ratio of the sum of the quantities of substances Bb11 and Bb12 to the amount of matter Bb2 is preferably from 0.95:1.05 of the mol. to 1.05:0.95 to say. Adduct Bb preferably has an acid number of from 5 to 60 mg/g, particularly preferably from 10 to 45 mg/g and most preferably from 15 to 40 mg/g

Hydroxyquinoline ethers, Bb11 preferably represent methyl, ethyl, n-propyl and n-butyl monoether of polyethylene glycol, where the polyethylene glycol has srednevekovoy molecular weight of from 500 to 4000 g/mol, particularly preferably from 750 to 3000 g/mol. The average number of hydroxyl groups in the molecule is preferably from 0.8 to 1.2, particularly preferably from 0.9 to 1.1. The most preferred polyethylene glycols, partly tarifitsirovannyim ethanol and having a molecular weight of from 1000 to 2000 g/mol.

Hydroxyquinoline ethers, Bb12 preferably represent methyl, ethyl, n-propyl and n-butyl monoether mixed ether of ethylene and 1,2-propylene glycols, where the mass fraction oxyethylene groups is from 10 to 85%, and the mass fraction oxypropylene groups ranges from 90%to 15%, calculated as the ratio of mass oxyalkylene groups, having two or three carbon atoms, respectively, and the sum of the masses of all oxyalkylene groups in mixed ether Bb12, and have srednevekovoy molecular weight of preferably from 500 to 10000 g/mol, particularly preferably from 1000 to 8000 g/mol. The average number of hydroxyl groups in the molecule is preferably from 0.8 to 1.2, particularly preferably from 0.9 to 1.1.

Anhydride Bb2 cycloaliphatic dicarboxylic acids preferably contain from 8 to 12 carbon atoms and is preferably selected from the group comprising tetrahydrophthalic anhydride, hexahydrophthalic anhydride and their homologues, such as methyltetrahydrophthalic anhydride or butyltetrahydrofuran anhydride. Unexpectedly found that cyclic acyclic anhydrides of dicarboxylic acids, such as maleic or succinic anhydride, may not be applied in the context of the present invention, because they degrade the compatibility of the pigment.

Basic acrylic copolymer what I resin And is a copolymer, at least three classes of vinyl monomers, each of which has at least one capable of copolymerization of olefinic unsaturation. It contains, at least, one containing the amino group of the monomer A1 vinyl type, which preferably contains at least one amino group, which particularly preferably is a tertiary amino group. Especially useful amidofunctional vinyl monomers are esters of tertiary aminoalcohols with acrylic or methacrylic acid, such as dimethylaminoethyl(meth)acrylate, dimethylaminopropyl(meth)acrylate, and amides, diamines with one tertiary and one primary groups, such as dimethylaminoethyl(meth)acrylamide, 3-N,N-dimethylaminopropyl(meth)acrylamide, and the corresponding diethylamino connection.

Other monomers A2 are linear or branched alkyl(meth)acrylates containing 1 to 13 carbon atoms in the alkyl group, such as methyl(meth)acrylate, ethyl(meth)acrylate, n-butyl(meth)acrylate, isobutyl(meth)acrylate and 2-ethylhexyl(meth)acrylate. Additional monomers present in the polymerization reaction leading to compound a, are hydrophilic vinyl monomers A3, with the remainder derived from polyethylene glycol or a mixed ether of ethylene and propylene, having masses of the new share at least 60% oxyethylene groups in the total mass oxyalkylene groups, polyether fragment having a molecular weight of preferably from 200 to 5000 g/mol, particularly preferably from 500 to 1500 g/mol, where one of the hydroxyl groups of polifonicos transformed into a simple ester group, preferably methyl, ethyl or boutelou ester group and the other hydroxyl group is removed by esterification with (meth)acrylic acid or other refinancing monocarboxylic acids, or by etherification with refinancing alcohol, such as allyl or metalalloy alcohol, or due to the formation of urethane by reaction with the adduct hydroxyalkyl(meth)acrylate and diisocyanate. Particularly preferably used monomers A3, which are adducts hydroxyethyl(meth)acrylate, an aromatic isocyanate such as toluylenediisocyanate or bis(4-isocyanatophenyl)methane, and polyethylene glycol with a molecular weight of from 200 to 5000 g/mol, esters of the specified glycol with (meth)acrylic acid and esters of the specified glycol with (meth)allyl alcohol. A mixture of two or more monomers A3 can also be used. Mass fraction of monomers A1, A2 and A3 is preferably from 15 to 40%, from 15 to 45% and from 30% to 60%, respectively, particularly preferred from 20 to 35%, from 20 to 40% and the 35% and 55%, respectively, and most preferably from 25%to 30%, from 25 to 35% and from 40% to 50% respectively. The polymerization is carried out, as usual, in solution with the use of alcohols, such as isopropanol, or ethers, such as butyl acetate as solvents, and azo - or peroxide catalysts, such as azobisisobutyronitrile, tert-AMYLPEROXY or tert-AMYLPEROXY.

It is also possible to copolymerization with the monomers A1 to A3 any other monomers A4, which are monomers of the vinyl type, i.e. they contain in their molecules at least one capable of copolymerization refinancing group. These monomers A4 can also be used in mixtures of two or more such monomers A4. Such monomers are preferably styrene, any isomers alkylthiols, especially methylsterols ("vinyl-toluene"), vinylnaphthalene, alkalemia esters refinancing of carboxylic acids, dialkyl ethers refinancing dicarboxylic acids, hydroxyalkyl esters of the same acids, unsaturated amides and NITRILES derived from such acids, alkylvinyl esters and alkalinisation. Acidic vinyl monomers such as acrylic or methacrylic acid, of course, less preferred.

Components a and b are mixed in a mass ratio of from 45 to 75% of a component a and from 55 to 25% component In preferably from 50 to 70% of component a and from 50 to 30% of component B, particularly preferably from 55 to 65% and from 45 to 35% Century

The pigments are inorganic and organic pigments. Examples of inorganic pigments include titanium dioxide, zinc oxide, carbon black, iron oxide, bismuth Vanadate, natural and burnt Sienna or umber, chromium oxide green, cadmium pigments, chromium pigments, etc. are Examples of organic pigments include phthalocyanines, chinagreen, hinaplanon, anthraquinones, isoindoline, parentani, indanthrene, derivatives dioxazine, diketopiperazines, azo-compounds, etc. may not Necessarily be added pigments and fillers such as clay, silica, talc, mica, wollastonite, wood flour and the like.

The pigment paste may be obtained from the paste resin AB and at least one pigment selected from the group comprising inorganic pigments and organic pigments. Preferably the paste is obtained by mixing the paste resin AB, at least one pigment, the homogenization of the mixture with a shift of obtaining pigment paste and mixing the specified pigment paste with a non-pigmented or white pigmented ink containing the organic binder of the paint. The organic binder of the ink is preferably chosen from the group comprising al is ednie resin, acrylic resin, modified acrylic alkyd resins, urethane Alcide and modified urethane-acrylic resin.

However, it can also be used other organic binding substances paints, such as polyurethane resins, individually or in a mixture with one or more of the above-mentioned binders. Thus obtained pigment paste can be used in combination with water-based paint or paint oil-based and offers all the combinations of color or tinting of paints with high gloss and good coloring ability.

In pigment pastes in accordance with the present invention can be obtained a high content of pigment without the use of large quantities of solvent. If you use organic pigments, pigment content, respectively, is in the range of mass fractions of from 5 to 45%, preferably 25 to 40%. If you use inorganic pigments, pigment content in mass should preferably be more than 10% wt. or even more preferably more than 60%. When using translucent pigments, such as semi-transparent iron oxide pigment in mass must be more than 5%, preferably above 20% or even 30% or more.

If desired, the pigment paste in compliance and with the present invention may also include defoamers, matting agents that prevent settling of pigment substances, agents that prevent the formation of a surface film, such as methylethylketoxime and/or other suitable additives.

The invention also relates to a method of kolorowania paint by selecting a base paint from a set of basic colors and the subsequent mixing of base paint with one or more of the above pigment paste. Although it is theoretically possible to mix all the colors, using one colorless basic dye, usually in the systems of kolorowania also use a base of white paint to get the colors with sufficient covering power.

Can be used different varieties pigmented base paints in white, if so desired.

Also typically use a limited number of pre-tinted base paints to increase the amount of mixed colors with sufficient hiding power. Also, if desirable, can be used separate base paint for gloss or itinerancy colors.

Pigment paste in accordance with the present invention are particularly useful as they can be used with a wide range of binder resins for paints, such as drying in air alkyd resin, acrylic resin and polyurethane resin, water-based, and alkene the resin or acrylic resin oil-based. This gives the paint with good gloss and excellent dispersion of the pigment, and with good fastness.

The following examples are intended to further illustrate the invention without limiting the scope of the claims, the features which are disclosed in the examples.

In the examples, all values of components in "%" are mass fractions unless stated otherwise.

The viscosity measured at 23ºC at the shear rate of 100 sec-1in accordance with ISO 3219. Mass fraction of solids ("fixed content") calculated in accordance with ISO 3251. The oil content represents the mass fraction of oil (oils) in the weight of the alkyd resin in the usual units of "%".

EXAMPLES

Example 1. The production of alkyd resins In

Adduct receive when interacting 929 g monometoksipolietilenglikolya having a molecular weight of 2000 g/mol, with 71 g tetrahydrophthalic anhydride in the presence of 1 g of triethylamine as a catalyst at 150 º C until, until it reaches a constant acid number of 26.5 mg/g

After cooling, 644 g of this adduct is mixed with 409 g of an alkyd resin having a hydroxyl number of 70 mg/g and an acid number of less than 3 mg/g, prepared from 160 g of sunflower oil, 72 g of benzoic acid as an agent of chain breakage, 100 g of phthalic anhydride and 100 g of pentaerythritol. To the mixture DOB is given in xylene in an amount of 10% by weight of the resin in the mixture, the resulting mixture was heated to 220º, and completely separate water, then distilled xylene. The remaining product has an acid number of less than 2.5 mg/g Dynamic viscosity of the resin is 9.5 PA·s when measured at a 50%aqueous solution. The viscosity does not change when stored for two weeks at 40 º C.

Example 2. Obtaining acrylic copolymer And

A mixture of 270 g of dimethylaminoethylmethacrylate, 50 g of butyl acrylate and 230 g of 2-ethylhexyl acrylate and 450 g of the adduct obtained by the interaction of 1 pray hydroxyethylmethacrylate, toluylene diisocyanate and dried nanometrology ether of polyethylene glycol with a molecular weight of 750 g/mol, added simultaneously with 20 g of tert-amaliastraat dissolved in 200 g of isopropanol for 5 hours to 330 g of isopropanol at the boiling under reflux and under stirring in nitrogen atmosphere. At the end of the addition the mixture is stirred for 1 hour, and then add 20 g of the solution of catalyst. When the reaction is stopped and the residual monomer concentration is 0.3%, the solvent is distilled at approximately 110 º C under reduced pressure. The reaction vessel is then washed with nitrogen and the reaction mass allowed to cool down to ambient temperature.

Example 3. Obtaining a paste resin

Alkyd resin of example 1 (600 g) and the acrylic resin of example 2 (400 g)is mixed after downloading both of the resin in the reactor for the production of resin and stirring at 80 ° C for 1 hour to obtain a homogeneous mixture. The heating off, while stirring is continued, and then add 1222 g of water for 30 minutes, then the reactor was allowed to cool down to ambient temperature. Get poluvyazkie, colorless solution of powdered resin having a mass fraction of solids of about 45%.

Example 4. Formulation of the basic colors white

4.1. White alkyd paint oil-based

Mix 303 g of alkyd resin oil-based (Vialkyd®AS 6172/55 SD60, Cytec Surface Specialties Austria GmbH, alkyd resin based on soya oil, with the oil content of 57%, dissolved in Shellsol®D60, mix With10-C12-paraffins and naphthenes having a low mass fraction of less than 0.1% of aromatic compounds), 67 g of Shellsol®D60 and 268 g of a white pigment of titanium dioxide (Kronos® 2190 Kronos Titan GmbH) and ground in a ball mill at room temperature for 30 minutes and then diluted with a mixture of another 303 Vialkyd®AS 6172/55 SD60, 6.7 g agent for preventing precipitation of the pigment (Additol®XL 297/100-based oxime, Cytec Surface Specialties Austria GmbH), siccatives a mixture of 16.8 g of each Octa-Soligen Cobalt®1, Octa-Soligen Calcium®2 and Octa-Soligen Zirconium®6 (dryers on the basis of octoate metal, Borchers GmbH, the number indicates the mass fraction in % of octoate metal in solution when used as a solvent Shellsol®D60) and 1.9 g increases the fluidity of the leveling additives (Additol ®VXL 4930 based on modified polyester silicone, Cytec Surface Specialties Austria GmbH). The obtained white paint (approximately 1000 g) had a viscosity, measured as described above, 542 MPa·s.

4.2. White alkyd paint water-based

Mix 395 g of alkyd resin water-based (Resydrol®AY 586w/38WA, modified acrylic alkyd resin, Cytec Surface Specialties Austria GmbH) and 254 g of a white pigment of titanium dioxide (Kronos® 2059 treated hydrophilic, Kronos Titan GmbH), a 21.5 g of a combined desiccant (Additol®VXW 4940, emulsion dryers on the basis of the connection, BA and Zr, diluted to a concentration of 50% deionized water, Cytec Surface Specialties Austria GmbH), 1.45 g of antifoam (based on liquid hydrocarbons, Additol®VXW 6211, Cytec Surface Specialties Austria GmbH) and 5.35 g increases the fluidity and leveling additives (Additol®XW 329 on the basis of modified polyester silicone, Cytec Surface Specialties Austria GmbH) and ground in a ball mill at room temperature for 30 minutes and then diluted with a mixture of another 268 g Resydrol® AY 586w/38WA, 5.35 g Additol®XL 297, 24.4 g of deionized water and 7.3 g of 25%aqueous ammonia solution. The obtained white paint (approximately 1000 g) has a viscosity, measured as described above, 949 MPa·s and a pH ranging from 8.5 to 9.0, measured at 10%dispersion in water.

Example 5. Obtaining pigment pastes

Colored pigment paste obtained from osteoblastoma resin according to the invention of example 3 as follows (mass components in g):

Table 1
Pigment paste in accordance with the invention
Pigment paste5,15,25,3of 5.4
The resin of example 340,3040,3040,3035,40
Deionized water22,5022,5022,5022,40
Additive (1)0,200,200,201,20
Additive (2)2,002,002,002,0
Pigment35,0035,0035,0040,0
Color pigmentYellow (3)Red (4)Purple (5) Green (6)
(1) preservative additive based on isothiazolinone (Additol®VXW 6372, Cytec Surface Specialties Austria GmbH)
(2) the antifoam based on liquid hydrocarbons (Additol®VXW 6211, Cytec Surface Specialties Austria GmbH)
(3) Hostaperm®yellow H3G (yellow pigment 154)
(4) Hostaperm®red E3B (purple pigment 19)
(5) Hostaperm®violet RL special (violet pigment 23)
(6) Hostaperm®green GC01

Example 6. The results of applying the tinted paints

Commercial pigment paste water-based (Colanyl®, Clariant International Ltd.) and pigment paste oil-based (Hostaint®the same manufacturer) different colors, using pigment Hostaperm®yellow H3G (yellow pigment 154), Hostaperm®red E3B (purple pigment 19), Hostaperm®violet RL special (violet pigment 23) and Hostaperm®green GC01, compared with the pigment paste of example 5 is made from the same pigments as commercial varieties, but with the paste resin of example 3, by making the tinted paints from alkyd paints oil-based white example 4.1 and alkyd paints, water based white color of example 4.2.

Pigment paste 5.1-5.4 and for comparison a commercial pigment paste water-based and oil-bases is used as koleroga pastes for color inks on the basis of white paints of examples 4.1 and 4.2 in accordance with the following formulas:

32
Table 2
Formulation of paints (pigment paste and the weight of the pigment paste in g)
Parameters pigment pasteThe weight of the pigment paste in g for:
PaintViscosity in MPa·sThe mole fraction of the pigment in %white paint
(-1) oil-based example 4.1
white paint
(-2) water-based example 4.2
6.1-868355,05,0
S-706335,35,3
N-1700335,05,0
6.4-439355,05,0
S-580of 5.4of 5.4
6.6-300355,05,0
S-502305,85,8
N-1000208,88,8
6.9-326405,05,0
S-340504,04,0
N-970454,44,4

Paint 6.1, 6.4, 6.6 and 6.9 obtained using koleroga pastes 5.1, 5.2, 5.3 and 5.4 respectively. Paint S, S, S and S obtained using pigment pastes with water-based Colanyl®yellow H3G100, Colanyl®red V, Colanyl®purple RL131 and Colanyl®green GG131 respectively, and paint N, N and N obtained using the pigment is s pastes, oil-based Hostaint ®yellow AH3G100, Hostaint®purple ARL 100 and Hostaint®green GC30, respectively. The indexes "1" or "2" is added to the paint markings depending on whether the paint is made with 152 g of white paint 4.1 oil-based (mo) or 162 g of white paint 4.2 water-based (in).

The Shine and color saturation measured on the paint films obtained from these colors by using the frame of the applicator (BYK-Gardner PA-2056) when the film strength in the wet state 150 μm on the glass panel (10x15 cm), and dried for 24 hours at room temperature (21º). The results are summarized in table 3. The gloss is measured at room temperature (21º) and a relative humidity of 50% using gloss BYK micro-TRI-glossmeter, and color saturation assessed using the indicator "1", meaning the highest colorous ability, and "5"meaning the lowest colorous capability.

Table 3
The results of the tests of paints
Paint 6.xx are supported-1
(oil-based)
Paint 6.xx are supported-2
(water-based)
PaintShine 20ºGloss 60ºThe feast upon the face color Shine 20ºGloss 60ºColor saturation
6.1-is 83.892,0176,586,51
S-80,890,6575,686,51
N-82,391,8153,077,75
6.4-83,290,5175,185,11
S-80,988,24-573,584,53
6.6-82,689,81 71,384,32
S-80,186,9473,484,21
N-82,5of 89.13-462,480,75
6.9-83,190,7275,9to 85.23
S-81,087,7576,085,83
N-82,190,4266,181,55
white paint-76,586,7-

From this table it can be seen that the pigment paste made using a paste resin in accordance with the present invention, yielded positive results in combination with white water-based paint, which is comparable to results obtained with a commercial pigment paste is water-based; whereas commercial pigment paste oil-based in combination with the same water-based paint has less Shine and color intensity.

On the other hand, pigment paste, made using a paste resin in accordance with the present invention, with positive results in combination with the white paint is oil-based, comparable with the results obtained with a commercial pigment paste oil-based; whereas commercial pigment paste water-based in combination with the same paint oil-based has less Shine and color intensity.

Thus, the paste resin in accordance with the present invention has extremely good compatibility with paints on oil and aq is th basis in both cases shows the performance on a par with the same class of commercially available pigment pastes of modern technology without compromise for universal compatibility. Similar results were obtained when pigmented inks are prepared based on acrylic binders paints water-based and oil-based. Thus, for the compilation of paint is sufficient to prepare only one colorous pasta-based paste resin in accordance with the present invention for use with alkyd paints, water-or oil-based, as well as for use with acrylic paints, water-or oil-based, which eliminates the need to stock different pigment pastes for each of these binders in the paint.

Also found that the pigment paste prepared with paste resins in accordance with the present invention can be used in the case of hybrid resins based accelerandi alkyd resins, as well as in the case Ratanakiri and urethaneacrylate resins as binders paints, and also in combination with inorganic and organic pigment materials mentioned earlier.

An important impact of the monomers of the class A3 base acrylic copolymer resin best you can do is idet when comparing, when this class of monomers A3 is absent.

Example 7. Pigment paste of comparative acrylic copolymer resin

7.1. Comparative acrylic resin

A mixture of 250 g of dimethylaminoethylmethacrylate, 650 g of n-butyl acrylate and 100 g of hydroxyethylacrylate added simultaneously with a solution of 20 g of azobisisobutyronitrile in 70 g of methoxypropanol, for 8 hours in a glass vessel, containing 160 g of methoxypropanol at 85 º C, and the contents of the vessel are stirred in nitrogen atmosphere. After the addition was finished the reaction mixture is stirred for another two hours, then add 1 g of the same radical polymerization initiator, dissolved in 10 g of methoxypropanol, and the reaction mixture is stirred for another two hours. Add 20 g of methoxypropanol, and the mixture is allowed to cool to room temperature.

7.2. The mixture of alkyd and acrylic resins

In a glass reactor transfer 129 g of the solution of acrylic resin of example 7.1, the solvent methoxypropanol removed by distillation at 140º under reduced pressure. Then the reactor is washed with nitrogen and, after cooling to a temperature below 100ºC add 133 grams alkyd resin of example 1 and thoroughly mixed with acrylic resin at 80 ° C for one hour. The mixture is cooled with stirring by heating and adding 313 g of fully deionized water for 30 minutes. The reactor and gooderism allowed to cool to ambient temperature. Get a non-homogeneous mixture of resin and water, having a mass fraction of solids of about 45%.

7.3. Obtaining a pigment paste

Sample (30.1 g) of the mixture of example 7.2 is taken immediately after homogenization and before separation of the phases, mixed with 27.7 g of deionized water, 0.2 g of preservative based on isothiazolinone (Additol® VXW 6372, Cytec Surface Specialties Austria GmbH), 2 g of antifoam, based on liquid hydrocarbons (Additol® VXW 6211, Cytec Surface Specialties Austria GmbH) and 40 g of pigment hinkreonsok red (Pigment Violet 19, Hostaperm® Red E3B, Clariant Deutschland GmbH). The mixture is homogenized in a ball mill at room temperature (21º) for thirty minutes.

7.4. Preparation of the tinted paint

The tinted paint is prepared by adding 5 g of the pigment paste of example 7.3 to 152 g of white alkyd paint oil-based example 4.1. The Shine and color saturation measured on the paint films obtained from these colors by using the frame of the applicator (BYK-Gardner PA-2056) when the film strength in the wet state 150 μm on the glass panel (10x15 cm) and dried within twenty-four hours at room temperature (21º). The results are summarized in table 4. The gloss is measured at room temperature (21º) and a relative humidity of 50% using gloss BYK micro-TRI-glossmeter, and color saturation assessed using the indicator "1", meaning the highest colorous ability, and "5", snachalo the lowest colorous capability.

Table 4
The results of the use of paste resin,
made from comparative acrylic resin
PaintShine 20ºGloss 60ºColor saturation
7,451795

Similar results were obtained when using alkyd paints, water-based white paint of example 4.2) in combination with the pigment paste of example 7.3.

This comparison shows that the Shine and the color intensity is markedly improved in the tinted paints, if one component paste resin used hydrophilic modified core acrylic resin together with alkyd resins in accordance with the present invention. This positive effect is observed as in paints oil-based and water-based paints.

1. Paste resin AB, which is a mixture of a waterborne alkyd resin and acrylic base copolymer resin And, where basic acrylic copolymer resin And is a copolymer of at least three classes vinyls the x monomers, each of which has at least one capable of copolymerization of olefinic unsaturation, and vinyl monomers include at least one vinyl monomer of type A1 containing the amino group, at least one monomer A2 selected from the group including linear or branched alkyl(meth)acrylates containing 1 to 13 carbon atoms in the alkyl group, and at least one hydrophilic vinyl monomer A3 containing the residue obtained from polifonicos, which is a polyethylene glycol or a mixed ether of ethylene - and propylene glycol having a mass share at least 60% oxyethylene groups in the total mass oxyalkylene groups, where one of the hydroxyl groups of polifonicos converted to simple ester group and the other hydroxyl group is removed terifically with refinancing monocarboxylic acid or by etherification with refinancing alcohol, or by the formation of urethane by reaction with the adduct hydroxyalkyl(meth)acrylate and diisocyanate.

2. Paste resin AB according to claim 1, where with water-dilutable alkyd resin has an acid number of from 0.2 to 5 mg/g

3. Paste resin AB according to claim 1, where with water-dilutable alkyd resin based on the condensation product of an alkyd resin BA and adduct b1-C4-monoalkylated EPE is and b1 of polyoxyethyleneglycol or C 1-C4-monoalkyl ether b2 simple mixed ether of ethylene - and propylene glycol, or mixtures thereof, and anhydride b3 cycloaliphatic carboxylic acids, and where with water-dilutable alkyd resin In the ratio of the sum of the quantities of substances b1 and b2 to the amount of matter b3 is preferably from 0.95:1.05 of the mol. to 1.05:0.95 to say.

4. Paste resin AB according to claim 1, where the mass fraction of monomers A1 is from 15 to 40%, mass fraction of the monomer A2 is from 15 to 45%, and the mass fraction of monomers A3 ranges from 30%to 60%.

5. Paste resin AB according to claim 1, where the monomer A3 is a reaction product of monoether of polyethylene glycol, toluene diisocyanate and hydroxyethylmethacrylate.

6. Paste resin AB according to claim 3, where the alkyd resin BA is produced by deposition of one or more polyols Ba1 containing in the molecule two or more hydroxyl groups, one or more polybasic acids Ba2 and one or more fatty acids Ba3, which can be substituted or mixed with one or more triglyceride oils VA.

7. Paste resin AB according to claim 1, where the components a and b are mixed in a mass ratio of from 45 to 75% of a component a and from 55 to 25% of component C.

8. Pigment paste containing paste resin AB according to claim 1 and at least one pigment selected from the group comprising h the organic pigments and organic pigments.

9. The method of applying the paste resin according to claim 1, comprising mixing the specified paste resin AB, at least one pigment, homogenization of the mixture when shifting the effort from obtaining the pigment paste and the mixture specified pigment paste with a non-pigmented or white pigmented ink containing the organic binder of the paint.

10. The method according to claim 9, where the specified binder paint selected from the group comprising alkyd resins, acrylic resins, acrylic-modified alkyd resins, Ratanakiri and urethane-modified acrylic resin.

11. The method according to claim 9, where the paint is a water-based paint.

12. The method according to claim 9, where the paint is a paint oil-based.



 

Same patents:
Pigment paste // 2484112

FIELD: chemistry.

SUBSTANCE: invention relates to production of composite additives for plastisol dyes used in making toys and also to a pigment paste. The pigment paste contains dioctyl phthalate, titanium dioxide, disperplast and an iron oxide pigment, with the following ratio of ingredients, wt %: pigment grade titanium dioxide - 16-17, iron oxide pigment - 1.7-1.75, disperplast - 0.18-0.2, dioctyl phthalate - the balance.

EFFECT: low toxicity with improved quality by excluding pigment which is not broken up.

2 ex

FIELD: chemistry.

SUBSTANCE: invention relates to a dialdimine of formula , where R is a radical of formula , where R1 and R2 are either independently univalent hydrocarbon radicals with 1-6 C atoms; R3 is a hydrogen atom; R4 is a radical of formula , where R5 is a linear or branched alkyl radical with 1-12 C atoms, A is a C4-C10 diamine group DA with two primary aliphatic amino groups after removal of both primary aliphatic amino groups and containing two ether groups, Q is a diisocyanate group DI after removal of both isocyanate groups; n equals 0 or an integer from 1 to 15; and where A and R do not contain groups which, in the absence of water, are capable of reacting with isocyanate groups. The invention also relates to a method of producing said dialdimine and use of dialdimine in emulsions for use as a curing or accelerating component for polymers with isocyanate groups.

EFFECT: invention provides two-component compositions which are fast-hardening and have exclusively high strength in the early period and do not have undesirable weak points.

22 cl, 2 tbl, 4 ex, 11 dwg

FIELD: process engineering.

SUBSTANCE: invention relates to multilayer combined materials. Proposed material comprises: top layer of textile web with porous polymer layer applied on its wrong side, adhesion layer and bottom layer. Porous polymer layer is formed on said working side and consists of the following components in wt %: polyesterurethane - 92.08-94.84; dimethyl formamide - 0.759-1.106; surfactant - 0.759-1.106; di-(2-ethylhexyl)phthalate - 0.759-1.106; microcrystalline cellulose - 2.884-4.604. Said composition is diluted by dimethyl formamide to viscosity of 170-180 poises.

EFFECT: optimised thermophysical and hygienic properties.

6 cl, 5 tbl, 2 ex

FIELD: chemistry.

SUBSTANCE: invention relates to a method of producing a latex paint composition containing biocides. The method of producing a paint composition involves preparation of a ground phase by mixing one or more pigments, other components of the ground phase and a biocide which is insoluble in water and mixing the ground phase with one or more latex resins and other liquefying components, where the biocide which is insoluble in water is a composition with high content of solid particles which preferably contains at least 50 wt % biocide. Components of the ground phase are selected from one or more components such as: cosolvents, coalescence agents, thickeners, surfactants, pigment dispersers, neutralising substances and antifoaming agents. Liquefying components are selected from one or more components such as: latex resins, pigment suspensions, coalescence agents, thickeners, neutralising substances and antifoaming agents. The water-insoluble biocide is particularly 1,2-benzisothiazol-3(2H)-one and is a composition with high content of solid particles which preferably contains at least 80 wt % biocide. The invention also relates to a ground phase for use in the method of producing latex paint which contains one or more pigments, ground phase components and a biocide which is insoluble in water, said biocide being a composition with high content of solid particles which preferably contains at least 50 wt % biocide. Components of the ground phase are selected from one or more components such as: water, cosolvents, coalescence agents, thickeners, surfactants, pigment dispersers, neutralising substances and antifoaming agents.

EFFECT: method enables to include a biocide in a form which does not contain volatile organic compounds.

11 cl, 3 tbl

FIELD: chemistry.

SUBSTANCE: present invention relates to versions of a water-based coating composition which is suitable for use particularly in the aerospace field. The water-based coating composition contains: (a) an essentially anhydrous basic component containing at least one hydrophilic polyol resin and at least one hydrophobic polyol resin, (b) an activating component containing at least one hydrophobic polyisocyanate and (c) water, wherein said composition contains 1-3 wt % of an organic solvent of the total weight of the water-based coating composition and component (a), (b) and (c) are mixed shortly before applying the water-based coating composition. In one version of the composition, the hydrophilic polyol resin can be selected from a group consisting of polyesters, polyethers, polyurethanes, caprolactones, alkyde resins and combinations thereof. Described also is a coating made using the polyurethane compositions disclosed herein.

EFFECT: obtaining water-based coating compositions which are stable during storage and have significantly low content of volatile organic compounds, coatings from which have improved technical characteristics such as impact resistance, specular gloss and longevity.

15 cl, 17 tbl, 7 ex

FIELD: chemistry.

SUBSTANCE: invention relates to pipeline construction and is used in field and basic conditions when laying underground main pipelines for protection thereof from corrosion, mechanical damage and during construction of gas or liquid transporting field and industrial pipelines in conditions of permanently frozen soil, when laying pipelines on swamps, on waterlogged areas, particularly for repairing anti-corrosion coatings of oil pipelines, oil product pipeline and gas pipelines during repair thereof in field conditions, including without stopping transportation of the product, and during corrosion protection of piping of compressor stations at pipeline temperature of 70-90°C, on a section of a pipeline transporting gas at temperature above zero after a compressor station, e.g. at a section of a discharge line transporting compressed gas at temperature of plus 40°C. Versions of anti-corrosion paint for obtaining an external polyurethane two-component protective coating are given. The paint is obtained by mixing component A and component B - polyisocyanate based on diphenyl methane diisocyanate with equivalent mass of 131-135. Component A is a suspension of substances in a hydroxyl-containing polyatomic alcohol with ether and ester bonds with equivalent mass of 230….250.

EFFECT: providing high rate of hardening of the coating with improved protective properties thereof, which prevents development of underfilm and stress corrosion on the pipeline for a period of time comparable with the life of the pipeline.

6 cl

Coating composition // 2479609

FIELD: chemistry.

SUBSTANCE: composition contains the following, wt %: 19.4-24.30 - polyester - polydiethylene glycol adipate with molecular weight of 800, 0.22-1.16 - dicyandiamide, 44.76-48.94 - aromatic isocyanate - 4,4'-diphenylmethane diisocyanate or polyisocyanate based on 4,4'-diphenylmethane diisocyanate, 0.99 - dye and organic solvent - the balance.

EFFECT: improved processing and operational characteristics of the composition, the coating from which has improved strength, chemical resistance to acid solutions, alkali solutions and mixtures of solvents, high thermal stability and hydrolytic stability.

2 tbl, 10 ex

FIELD: chemistry.

SUBSTANCE: aqueous dispersion contains the following structural components: (A) 10-40 wt % of one or more aliphatic polyisocyanate compounds; (B) 40-70 wt % of at least one polyhydroxy compound having molecular weight Mn ranging from 400 g/mol to 8000 g/mol; (C) 19-49 wt % of a non-ionically hydrophilising monofunctional polyoxyalkylene ether which contains only one hydroxyl or amino group and 50-100 wt % of structural components derived from ethylene oxide, and having molecular weight Mn ranging from 1200 g/mol to 3000 g/mol; (D) 0.5-10 wt % of at least one polyamine compound having molecular weight Mn ranging from 32 g/mol to 400 g/mol and functionality greater than or equal to 1; (E) 0.5-10 wt % of a polyhydroxy compound having molecular weight Mn ranging from 62 g/mol to 320 g/mol and functionality greater than or equal to 1; and (F) 0-10 wt % of auxiliary substances and additives; wherein the sum of said structural components (A) through (F) equals 100 wt %.

EFFECT: obtaining novel aqueous polyurethane carbamide dispersions which have sufficiently high storage stability.

6 cl, 9 ex, 2 tbl

FIELD: nanotechnology.

SUBSTANCE: invention relates to a method of obtaining a nanocomposite material for thermal and chemoresistant coatings and planar layers with high dielectric capacitivity. The method is proposed in which, as the polymer binder the poly (o-hydroxy amide) is used - a product of polycondensation of 3,3'-dihydroxy-4,4'-diamino-diphenylmethane and isophthalic acid dichloride in amide solvent, and as a filler the ferroelectric material nanopowder CTSNV-1 Pb0.81 Sr0.04Na0.075Bi0.075(Zr0.58Ti0.42)O3 at a weight ratio of poly(o-hydroxy amide): filler from 1:1.15 to 1:1.5. The ratio of components in the nanocomposite (wt %): poly(o-hydroxy amide) 6-12; filler CTSNV-1-6.9-18, solvent - the rest. Mixing of the components is carried out at room temperature without preliminary dispersion of ferroelectric filler, before applying to the conductive substrate the nanocomposite suspension is subjected to ultrasonic treatment. Films formed on the conductive surfaces are dried at 95-100°C and subsequent stepped heat processing in the temperature range of 200-350°C.

EFFECT: obtained coatings are chemically stable, have a heat resistance up to 400°C, high adhesive capacity to various types of substrates and dielectric capacitivity ε of 23 to 185.

1 cl, 1 tbl, 9 ex

FIELD: chemistry.

SUBSTANCE: present invention relates to a double-component coating composition (2C), as well as a coated article, a method of making a coated article and use of material which contains a phosphorus-containing polyol as a fireproof material in the disclosed composition. The composition contains: (a) first component containing isocyanate, wherein said isocyanate contains a prepolymer having isocyanate functional groups formed from a reaction mixture containing isocyanate and a material containing a phosphorus-containing polyol with the equivalent ratio of isocyanate groups to hydroxyl groups greater than 1 and the phosphorus-containing polyol which acts as fireproof material is (i) a product of reaction of the source phosphorus-containing polyol, selected from polyphosphate polyols, polyphosphite polyols, polyphosphonate polyols and mixtures thereof and compounds having epoxy functional groups; or (and) a product of reaction of a phosphorus-containing acid, a compound having epoxy functional groups and, optionally, a phosphorus-containing polyol; and (b) a second component containing a polyamine, wherein the first and second components are stored separately and form polyurea after mixing and the composition further contains an additional fireproof material which is added to the first and/or second component and is selected from graphite, halogenated phosphates, phosphates without a halogen, tris(2-chloropropyl)phosphate, tris(2,3-dibromopropyl)phosphate, tris(1,3-dichloropropyl)phosphate, diammonium phosphate, powdered or pyrogenic silicon dioxide, sheet silicates, aluminium hydroxide, bromated fire-retardants, halogenated aromatic compounds, antimony oxide, aluminium oxide trihydrate, metal borates, zinc borate, barium metaborate pentahydrate, ester phosphates, polyvinyl chloride, melamine cyanurate, melamine phosphates, polymelamine phosphates, melamine pyrophosphates, polylmelamine pyrophosphates, melamine borate, other melamine derivatives and mixtures of compounds.

EFFECT: obtaining a double-component coating composition, having improved fire-resistance and heat-resistance.

12 cl, 7 ex, 1 tbl

FIELD: chemistry.

SUBSTANCE: present invention relates to making coatings from aqueous dispersions and an aqueous dispersion containing at least one alkyd resin and at least one polymerisate having at least one (meth)acrylate segment. The (meth)acrylate segment contains 1-30 wt % of structural units derived from (meth)acrylates which in the alkyl residue have at least one double bond and 8-40 carbon atoms, 0.1-10 wt % of structural units derived from monomers containing acid groups, and 50-98.9 wt % of structural units derived from (meth)acrylates having 1-6 carbon atoms in the alkyl residue, based on the weight of the (meth)acrylate segment.

EFFECT: invention enables to obtain dispersions with prolonged storage stability and coatings with high mechanical strength.

39 cl, 2 tbl, 7 ex

FIELD: chemistry.

SUBSTANCE: invention relates to production of paint materials. The paint composition is prepared by mixing varnish with fine powder of an inorganic material. The powder of inorganic material used is water treatment sludge sieved through a No.0056 sieve, said sludge being formed as a result of removing hardness salts during water treatment at thermal power plants. Components are in the following ratio, wt %: varnish 35-65; said powder of water treatment sludge 35.0-65.0.

EFFECT: method is simple and enables to obtain dough-like and ready-to-use paint compositions.

FIELD: chemistry.

SUBSTANCE: polystyrene paint composition contains the following, wt %: film-forming agent - polystyrene or derivatives thereof 1-9, pigments 1-20, colloxylin 5-15, alkyd resins 10-15, plasticiser 1-15 and solvents - the balance.

EFFECT: obtaining coatings which provide high degree of protection from corrosion of components and surfaces in conditions of atmospheric exposure or exposure to a liquid or moist environment.

2 ex

FIELD: metallurgy.

SUBSTANCE: electrical steel coating method using lacquer composition for charged core involves application at least of one coating layer of lacquer composition and curing of the applied layer. Lacquer composition for charged core contains 5-95 wt % at least of one alkyd resin with OH nucleophilic groups, 0-70 wt % at least of one polyamid resin containing groups of amide of α-carboxy-β-oxocycloalkylcarboxylic acid, and 5-95 wt % at leas of one organic solvent and/or water. Weight fraction in percents is calculated relative to total weight of the coating composition.

EFFECT: method ensures excellent adhesion and corrosion resistance of coatings, as well as compliance with high-profile standards in combination with various technical requirements.

10 cl, 3 tbl

FIELD: chemistry.

SUBSTANCE: composition for fixing wrapping articles contains A) 1-60 wt % of at lest one resin of α,β-unsaturated polyether based on at least one unsaturated mono-, di- or tricarboxylic acid and/or substance containing molecules with mono-, di- or tricarboxylic acid groups, at least one polyol, B) 0.1-80 wt % of at least one inorganic and/or an organic-inorganic hybrid component, having functional groups for reaction with components A) and C), where said hybrid components are polymers or colloidal solutions based on silicon, titanium or zirconium and oxygen atoms, which contain hydroxyl and/or alkoxy groups and/or hydroxyalkyloxy groups and/or organic fragments, which have epoxy and/or isocyanate and/or unsaturated groups, C) 2-80 wt % of at least one monomer and/or oligomeric unsaturated component, which is styrene, vinyl toluene, hexanediol dimethacrylate, butanediol dimethacrylate and/or (meth)acrylates of products of a polyaddition reaction of ethylene oxide with trimethylolpropane capable of reaction with components A and B, and D) 0-15 wt % conventional additives, where wt % is calculated relative the total weight of the composition.

EFFECT: excellent heat conductivity properties and high level of electrical insulation along with excellent adhesion and thermal stability.

6 cl, 1 tbl, 2 ex

Liquid hardening // 2447114

FIELD: chemistry.

SUBSTANCE: invention relates to curing agents for air-drying alkyd-based resins, coating compositions, such as paint, varnish, wood stain, inks and linoleum floor coverings. Described is a curable liquid medium containing a) from 1 to 90 wt % of an alkyd-based resin and b) from 0.0001 to 0.1 wt % of a siccative in form of an iron or manganese complex with a tetradentate, pentadentate or hexadentate nitrogen donor ligand.

EFFECT: said siccative has high activity and enables hardening of compositions at relatively low concentration in a curable liquid medium.

19 cl, 8 tbl, 5 ex

FIELD: metallurgy.

SUBSTANCE: binding consists of cross-linking agent and branched poly-ether with partially remote functional groups with acidic functional groups. Said branched poly-ether consists of at least one multi-functional component, of at least one di-functional component reaction capable relative to a functional group of multi-functional component and at least one mono-functional component containing fat acid. Temperature of poly-ether vitrification is 40°C or more.

EFFECT: production of binding applicable for compositions of powder coating where binding improves corrosion resistance.

12 cl, 3 tbl, 2 ex

FIELD: chemistry.

SUBSTANCE: composition contains the following in wt %: 16-23 film-forming agent; 38-40 mixed pigments; 2.0-3.0 organic complexing agent - tanning and derivatives thereof; 1.0-2.0 inorganic filler - talc; 3.0-4.0 mixture of C2-C4 alcohols and an organic solvent - the rest. The film-forming agent is 12-15 wt % alkyd varnish and additional 4-8 wt % synthetic chlorinated rubber. The mixed pigments are in form of a mixture of zinc oxide, zinc powder and micaceous iron. The mixture of alcohols contains ethyl alcohol, butyl alcohol and isobutyl alcohol in ratio 1.0:1.0:1.4. The invention enables to obtain compositions with service life of coatings of at least 10-15 years.

EFFECT: coatings have good impact properties and high rate of drying, priming composition does not require surface mechanical pre-treatment in order to remove scales and rust.

6 cl, 3 tbl, 3 ex

FIELD: chemistry.

SUBSTANCE: composition contains the following, wt %: alkyde primer 90-98, organosilicon amide of perfluorocarboxylic acid of formula C3F7OCF(CF3)CF2OCF(CF3)CONH(CH2)3Si(OC2H5)3 1-5 and 1-5 product of reaction of boric acid, diethanolamine and fatty acid of plant oil. The fatty acid of plant oil is selected from oleic acid, linoleic acid and linolenic acid, in molar ratio of 1:4:2, respectively.

EFFECT: invention enables to obtain anticorrosion coatings with good physical-mechanical and water-, oil- and gasoline-resistant properties.

3 tbl, 5 ex

Composite oil paint // 2415897

FIELD: chemistry.

SUBSTANCE: invention is used in shipbuilding, construction works in shafts, for repair works on metallurgical factories, for painting concrete and plastered structures, for painting metal structures, wooden structures and slate roofing. The paint contains components in the following ratio in wt %: film-forming agent 50-90, titanium dioxide and/or chalk 0.1-32.0, cement and/or cement dust 0.1-30.0, siccative 0.5-5.0, microtalc and/or micromica or sand and/or lime or lime milk and/or flue ash and/or microcalcium and/or sulphanol and/or iron oxide - the rest. The film-forming agent contains components in the following ratio in wt %: pentaphthalate and/or glyphtal lacquer or mixture thereof with nitrocellulose and/or perchlorovinyl and/or ethylcellulose and/or coal-tar varnish 1-55.0, drying oil or masut or bitumen 1-45.0, bustilat and/or liquid glass 1-10.0, water and/or nefras and/or solvent and/or benzine and/or solvents 647, 646, 650, 651 3-20.0, sulphanol or butyldiglycol - the rest.

EFFECT: paint film has good adhesion to surfaces, coating does not crack during bending and sharp change in temperature, paint film has high resistance to water, acid, alkali, benzene, the paint can be applied on a rusty, oily or wet surface, does not form a dried up film during storage and is environmentally safe.

3 cl, 4 tbl, 70 ex

FIELD: chemistry.

SUBSTANCE: composition contains 55.5-86.2 pts.wt aqueous dispersion of a copolymer with particle size of not more 0.1 mcm, containing 35.5-38.0 wt % butyl acrylate, 16.5-18.0 wt % 2-ethylhexyl acrylate, 10.0-11.0 wt % methyl methacrylate, 13.5-15.0 wt % styrene, 14.0-15.0 wt % α-methyl styrene, 5.0-5.5 wt % methacrylic acid, and 13.8-44.5 pts.wt aqueous solution of isopropyl alcohol mixed with water in ratio 1:1-3:1. The aqueous acrylic dispersion can additionally contain triallyl isocyanurate and/or vinyl triethoxy silane. The primer composition can additionally contain a wetting agent, an antifoaming agent, complexing agents, adhesive and biocidal additives.

EFFECT: improved continuity and adhesion strength of a polymer coating on aluminium foil, which ensures strong adhesion of printing ink on foil.

4 cl, 2 tbl, 24 ex

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