• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Binders for cathodically depositable aqueous coating compositions comprising the reaction product of (A) one mole polyisocyanate with (B) at least one mole dialkylalkanolamine and a monohydroxyalkyl(meth)acrylate and/or monohydroxyalkoxy(meth)acrylate and/or a monohydroxyallylether of a polyol. Optionally, there can be included a saturated and/or unsaturated fatty alcohol or fatty acid. The binders have an NCO-value of substantially zero; a molecular weight of from about 500 to 5000, and in each 1000 molecular weight unit a basic content of from about 0.5 to 3 and a double bond content of from about 0.5 to 4. The binders in coating compositions cure at relatively low temperatures and relatively short curing times to provide films having excellent resistance to water, chemicals, and corrosion.
    公开号:SU871738A3
    申请号:SU782565899
    申请日:1978-01-18
    公开日:1981-10-07
    发明作者:Пампоухидис Георгиос；Хениг Хельмут
    申请人:Вианова Кунстхарц Аг (Фирма)；
    IPC主号:
    专利说明:

    one
    The invention relates to the field of producing polyurethane coatings, in particular coatings deposited on a cathode, and can be used in the paint industry.
    A known method for producing polyurethane coatings, occluding ttilx on a cathode, by electroplating a binder obtained by reacting the JQ of the isocyanate component with compounds containing an active hydrogen atom, followed by curing by heating (1.
    . 15
    However, during the curing process, a significant amount of toxic products is released, which makes the process low-tech.
    The closest to the invention to the technical essence is the method of obtaining urethane coatings deposited on the cathode by reacting the isocyanate component with a compound containing an active hydrogen atom, followed by partial or complete neutralization with inorganic or organic acids C2B30
    However, the resulting coatings are not strong enough in conditions of high humidity.
    The aim of the invention is to increase the stability of the final product against saline mist, as well as to reduce the amount of toxic decomposition products during firing of coatings.
    This goal is achieved by the fact that upon receipt of the installation coatings deposited on the cathode by reacting the isocyanate component with the compound containing the active hydrogen atom, followed by partial or complete neutralization with inorganic or organic acids, di- or tri-isocyanate component is used alone or in mixture with 1-1,5 mol. dialkylalkanolamine and 0.7-2 mol of monohydroxyalkyl (meth) acrylate and / or monohydroxyl allyl ether of a polyhydric alcohol, with 25-50 mol,% of this unsaturated Nogo compounds may be replaced by unsaturated monohydric alcohol having 12 - 24 carbon atoms.
    The proposed method of coating is obtained by interaction in one or
    several stages 1 mol of the corresponding isocyanate with a minimum of 1 mol of dialkylalkanolamine and 1-3 mol of the corresponding saturated or unsaturated hydroxyl or carboxyl component at 20-80 s, the reaction can also be carried out in the presence of a solvent inert with respect to the isocyanate and a catalyst active with respect to isocyanate.
    Suitable polyisocyanates are, for example, aromatic isocyanates of the type 2,4- or 2.6-toluene diisocyanate or the products of their di- or trimerization, 4,4-diphenylmethane diisocyanate, 4,4, 4-triphenylmethanate triisocyanate, trimethylol propane-tris-toluenylisocyanate, tris-cis-isocyanates, tri-methylispropane, 1-isocyanate, trimethylol propane trisulfuylenesocyanate, tris (I-cis). ) - to phosphate, or cycloaliphatic isocyanates such as isophorone diisocyanate, cyclohexane 1,4 - diisocyanate, dimethyl diisocyanate, and aliphatic isocyanates like trimethylhexamethylene - 1,6-diisocyanate, trihexamethylene triisocyanate. Suitable dialkylalkanolamines are, for example, dimethylethanolamine, diethylethanolamine and their higher glogologists or isomers.
    Suitable polymerizable monohydroxy compounds are, for example, hydroxyalkyl esters of acrylic or methacrylic acid, tri- or tetrapropylene glycol-mono (meth) acrylates, trimethylol-propanediyl ester, tri-ethyl ester of pentaerythritol.
    . Saturated alcohols can also be partially used as monohydroxy compounds. Finally, saturated or unsaturated monocarboxylic acids can also be partially used.
    The interaction of carboxylic acids with isocyanate, as is known, occurs with the elimination of carbon dioxide.
    As the unsaturated aliphatic fatty alcohols, 10-undecan-1-ol can be used; 9c-octadecen-1-ol (oleyl alcohol); 9-t-OKtacen-1-ol (elaidyl alcohol); 9c, 12c - octadecadien-1-ol (linoleyl alcohol); 9c, 12c, 15c-octadecatrien-1-ol (linolenyl alcohol); 9-o-eikozen-1-ol (gadoleyl alcohol); IScDVAS-1-ol (erucic alcohol); 13-t-docosen-1-ol (brassidyl alcohol).
    Saturated mono-alcohols containing at least 6 carbon atoms can also be used to improve bottling.
    As such, hexanol, nonanol, decanol and other homologues thereof, for example dodecanol (lauryl alcohol), octadecainol (stearyl alcohol), and alkyl alcohols such as 2-ethylhexanol, 2-pentylponanol, 2-decyl tetradecanol, can be used.
    Unsaturated fatty acids can be, for example, linoleic, oleic, linoleic acids and other acids found in natural oils or in modified natural oils. The same applies to saturated monocarboxylic acids.
    As saturated or unsaturated monocarboxylic acids may,
    5 20 25 finally, polyester anhydrides of dicarboxylic acids with mono-alcohols are also used.
    The amino groups of the cationic components are partially or fully neutralized by organic and / or inorganic acids, for example, formic, acetic, lactic, phosphoric.
    The degree of neutralization in each case depends on the properties of the binder used. In general, so much acid is added so that the coating agent has a pH of 4-9, preferably 5-8, and can be easily diluted with water or dispersed.
    The concentration of the binder in water depends on the parameters of the method during the processing by the method of electrical loading and is in the range of 2-30 wt.%, Preferably 5-15 wt.%.
    When deposited, the initial composition comes into contact with the electrically conductive anode and the electrophore cathode, while the cathode surface
    about 35 is coated. The coating layer can be applied to various electrically conductive substrates, in particular metallized, such as steel, aluminum, copper, and also to metallized polymer materials or materials having an electrically conductive coating layer.
    After deposition, the coating layer is cured at an elevated temperature of 130-200 ° C, preferably 150-180 seconds. The cure time is 5-30 minutes, usually 1.0-25 minutes.
    5 50 55
    Examples 1-12. 1 mol of the corresponding polyisocyanate is diluted with a solvent inert to the isocyanate to a concentration of the target product of 60% and with stirring under conditions that exclude the presence of moisture, the compound capable of reacting with the isocyanate is added in an amount of 20-60 seconds for 1 hour equivalent to the amount of isocyanate. Then, the reaction mixture, whereby a polymerization inhibitor can also be used, is reacted with BO-SCO until the magnitude of 65 NCO is less than 1.
    .
    Below are the molar ratios of the reaction components (examples 1–12).
    EGA - ethyl glycol acetate (monoethylene glycol monoethyl acetate) DMF - dimethylformamide
    TDI - toluylenediocyanate (marketable product - a mixture of zomers)
    IPDI - isophoroidiisocyanate TFMT - triphenide methane triisocyanate TMPTTI - trimethylpropantristoluenilisocyanate TIFTP - tris- (4-isocyanatophenyl) -thiophosphate
    d- dimethyl diisocyanate DMEL dimethyl ethanol amine DMP dimethyl propanol amine HEM hydroxyethyl methacrylate GBA hydroxy butyl acrylate TPGMM tripropylene glycol monomethacrylate
    OS - oleic alcohol TMPDM - trimethylolprbpandimethacrylate
    PETM - pentaerythritol methacrylate PETAE - pentaerythritol triethyl
    ether
    The calculated molecular weights, the number of basic nitrogen atoms for every 1000 units of molecular weight, and the number of polymerizable double bonds for every 1000 units of molecular weight are given in Table. one.
    For this test, non-pretreated cleaned steel sheets are coated with a pigmented lacquer which contains (based on 100 parts by weight of hard resin; 20 parts by weight of 5 aluminum silicate pigment and 2 parts by weight of carbon black.
    Test bout zich according to examples 1-12.
    A sample of 100 g of solid resin is sampled from each of the abovementioned Q agents, treated with an appropriate acid and diluted with stirring with deionized water to a weight of 1000 g. 10% solutions are precipitated using the cathodic fob method on a steel sheet. The deposition time in all cases is 60 s.
    The material with the coating layer is then washed with demonized water and cured at elevated temperature. Get the film coated with a thickness of 13-17 nm.
    In tab. 2 shows the test results.
    Table 1
    670
    927
    1007
    1046
    1146
    1062
    1173 1173
    1314 1361 1397 1160 1174
    3.00
    2.16

    2.04
    2.3
    3.55
    2.91
    3.4 3.4
    2.66
    2.94
    3.2
    2.6
    权利要求:
    Claims (2)
    [1]
    2.65 Claims of Invention A method of producing urethane coatings deposited on a cathode by reacting an isocyanate component with a compound containing an active hydrogen atom followed by partial or complete neutralization with inorganic or organic acids, in order to increase the stability of the final product against saline mist, as well as reducing the amount of toxic decomposition products during annealing of coatings, di- or triisocyanates are used as an isodioate component, alone or in 1-1.5 mol of dialkylssccanolamine and 0.7-2 mol of monohydroxyethyl (meth) acrylate and / or monohydroxyallyl ether of polyhydric alcohol are mixed with 25 to 50 mol% of this unsaturated compound which can be replaced by unsaturated monohydric alcohol containing 12 to 24 atoms carbon. Sources of information taken into account in the examination 1. US patent number 2726216, cl. 252-313, published. 1955.
    [2]
    2. US patent 3883483, cl. 260-77.5, publ. 1975 (prototype).
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    同族专利:
    公开号 | 公开日
    AT346988B|1978-12-11|
    DE2732955B2|1979-09-27|
    GB1578413A|1980-11-05|
    JPS53118437A|1978-10-16|
    FR2379587B1|1982-06-04|
    US4179425A|1979-12-18|
    ATA75777A|1978-04-15|
    IT1093478B|1985-07-19|
    DE2732955A1|1978-08-10|
    ES466685A1|1978-10-16|
    IT7819845D0|1978-01-31|
    FR2379587A1|1978-09-01|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3883483A|1971-08-02|1975-05-13|Ppg Industries Inc|Electrodepositable cationic thermosetting coating compositions|
    DE2249446C3|1972-10-09|1979-02-15|Basf Farben + Fasern Ag, 2000 Hamburg|Use of a coating agent curable by ionizing radiation for coating surfaces|
    US3939126A|1974-09-05|1976-02-17|Union Carbide Corporation|Acrylyl-terminated urea-urethane compositions|AT356226B|1977-10-24|1980-04-10|Vianova Kunstharz Ag|METHOD FOR PRODUCING CATHODICALLY DEPOSIBLE BINDERS|
    AT357247B|1978-12-27|1980-06-25|Vianova Kunstharz Ag|METHOD FOR THE PRODUCTION OF SELF-CROSS-LINKING BINDING AGENTS FOR CATHODICALLY DEPOSITABLE ELECTRO DIP COATINGS|
    DE3124088A1|1981-06-19|1983-01-05|Basf Ag, 6700 Ludwigshafen|BATH COMPOSITION FOR CATAPHORETIC ELECTRO DIP PAINTING|
    EP0443537A3|1990-02-20|1992-05-06|Takeda Chemical Industries, Ltd.|Water soluble photocurable polyurethane polyacrylate, adhesives containing the same, and production of laminated articles|
    GB2270916A|1992-09-23|1994-03-30|Sericol Ltd|Urethaneacrylates|
    ES2111933T3|1993-06-22|1998-03-16|Basf Coatings Ag|AQUEOUS ELECTRO-IMMERSION LACQUERES AND LACQUERING PROCEDURE OF ELECTRIC CONDUCTING SUBSTRATES.|
    DE4332014A1|1993-09-21|1995-03-23|Basf Lacke & Farben|Electrocoating lacquers and methods for lacquering electrically conductive substrates|
    US6025068A|1998-02-13|2000-02-15|Ppg Industries Ohio, Inc.|Inkjet printable coating for microporous materials|
    DE19958488A1|1999-12-04|2001-06-21|Dupont Performance Coatings|Aqueous electrocoating paints, their manufacture and use|
    JP5229501B2|2009-09-02|2013-07-03|荒川化学工業株式会社|Active energy ray curable resin, active energy ray curable resin composition, coating agent and plastic molding|
    JP5201125B2|2009-12-15|2013-06-05|荒川化学工業株式会社|Urethaneacrylate resin, active energy ray-curable resin composition, coating agent and plastic molding|
    WO2013113739A1|2012-02-01|2013-08-08|Bayer Intellectual Property Gmbh|Low-viscosity, cationically hydrophilised polyurethane dispersions|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    AT75777A|AT346988B|1977-02-07|1977-02-07|PROCESS FOR THE PRODUCTION OF CATHODICALLY SEPARABLE URETHANE BINDERS|
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