• 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:

    公开号:SU971105A3
    申请号:SU792732900
    申请日:1979-03-12
    公开日:1982-10-30
    发明作者:Нахткамп Клаус；Педаин Иозеф；Граммель Юрген
    申请人:Байер Аг(Фирма)；
    IPC主号:
    专利说明:

    3971 dots are added after mixing the prepolymer with an extension. When carrying out the method uses chemically unrelated emulsifiers. Ionic emulsifiers, such as alkali metal or ammonium salts of long chain fatty acids, or long chain aryl (alkyl) sulfonic acids, and nonionic emulsifiers, such as ethoxylated alkyl benzenes with an average mol. weighing 500-10000. Before carrying out the process, chemically unbound emulsifiers are intensively mixed with the prepolymer. Usually they are used in an amount of 1-30 weight. % preferably weight. %, based on the weight of the prepolymer. Along with prepolymer1, CO units are used which, as a result of hydrolysis, form hydrazine (products of the interaction of hydrazine with carbonyl compounds with an equivalent ratio between hydrazine NH groups and carbonyl groups of 1: 1-2: 1). For carrying out the method, the Npl-terminated prepolymer is mixed with azines and / or hydrazones at an NCO-rpynnbi / NH2-rpynnbi ratio equal to C: 1 - 1: 1, 5, preferably 1.3: 1-1: 1, Mixing components carried out at a temperature of from -20 to + 100 ° C, preferably at 15-60 ° C. Water is introduced into the system all at once or gradually in an amount sufficient to provide a high solids content (up to 40-60% by weight). The water temperature is 0-90 ° C, preferably 15 6 ,. The particle size of the resulting dispersions is 20–200 µm. The polyurethanes contained in the aqueous dispersion can be used, for example, for the manufacture of adhesives and coatings for textiles, paper, for skin finishing, and also as fiberglass. For coating on inelastic materials, hard and resistant coatings can be made, which are used, for example, as varnishes for wood and metal, followed by crosslinking, if necessary, with formaldehyde, urea and melamine resins. In addition, the resulting dispersions are suitable for mixing with aqueous dispersions of polyacrylate. Example 1. Source components: g polyester based on adipic acid and diethylene glycol (mol. Weight. 2550); 200 g of polyether-based polyether (initiator propandiol-1,2, mol. Weight SO-O); 85.8 g of polyether from 15 wt. % propylene oxide and 85. weight. % ethylene oxide (initiator n-butanol, mol. weight); 85.0 g of propoxylated adduct from 2-butendiol-1, and NaHSOj (mol. Weight 425); 9.3 g of p-toluenesulfonic acid methyl ester, 313.2 g of diisocyanatotoluene (a mixture of 80 wt.% 2,4- and 20 wt.% 2,6-isomers); 71.7 g of acetone azine (bis-isopropylidene-hydrazine); 3290 g of deionized water. A mixture of p-toluenesulfonic acid methyl ester is added to the mixture of polyester, both zohydrates and bisulfite adduct, which is dehydrated at 120 ° C (for binding, possibly contained in the bisulphite alkali adduct), and then at 60 ° C diisocyanatotoluene. Stir at 80 ° C until the NCO reaches 3.1 wt. , is then cooled to 50 ° C and acetonazine is mixed in to the evenly viscous melt of the prepolymer, the temperature slightly decreases and the viscosity decreases. With thorough mixing, water is introduced and stirred for two hours. The resulting dispersion has a solids content of 40% by weight. % viscosity, determined by Ford glass (nozzle diameter, mm), - 18 s. Dispersion in translucent light has a Tyndall effect. It dries to produce a transparent, soft elastic film and is suitable for application to elastic materials. Gluing the first layers of polyurethane varnish with such a dispersion provides coating on textile material with a soft neck and very good resistance to washing and dry cleaning. In addition, the dispersion is suitable as a primer for finishing leather. EXAMPLE 2 A prepolymer was prepared according to Example 1. After cooling to 50 ° C, 89.6 g of methyl ethyl ketazine was mixed in and dispersed as described in Example 1. The resulting dispersion is in / 1 flowable and exhibits a Tyndall effect. Example 6 Prepare the prepolymer according to example 1. After cooling to 50 ° C, 89.6 g of isobuty are mixed in.
    : raldezin and then dispersed as described in example 1. The resulting dispersion is fluid and exhibits a Tyndall effect.
    P r i m e r. Prepolyme was prepared according to Example 1. After cooling to 50 ° C, 30.1 g of acetohydrazone was added dropwise over 30 minutes, while the temperature and viscosity increased slightly, but without danger of gelation. Then dispersed as described in example 1. The viscosity of the dispersion obtained, determined by the Ford glass, is 17 seconds. In translucent light, dispersion has a Tyndall effect. It dries to produce a film, the properties of which correspond to the properties of the product obtained in Example 1.
    Example 5. Source components: 1710 g of polyester based on adipic acid and butanediol (mol. Weight 2250); 85.5 g of polyether from 15 wt. % propylene oxide and 85 wt. % ethylene oxide (initiator n-butanol, mol. weight. 2X5); 93.5 g of propoxylated adduct from 2-butenediol-1, ft and NaHSOj (mol. Weight); BOO g acetone; 550 g, α-diisocyanatodiphenylmethane, 125.2 g of acetonazine; 3700 g of deionized water.
    To a mixture of polyester, polyether and bisulfate adduct, dehydrated at 120 ° C, to decrease the viscosity j of the resulting prepolymer to 056
    600 g anhydrous acetone is added. Then 4, 4-diisocyanatodiphenylmethane is added and stirred at 60 ° C until the NCO value is reached. The obtained prepolymer is cooled to 20 ° C, then acetonazine is added, and no reaction between the azine and the isocyanate groups is observed. Under intensive mixing, it is dispersed by adding water.
    In the resulting dispersion, the acetone content is 10 wt. % The dispersion can be freed from acetone by vacuum distillation, after which the solids content is 40 wt. % The viscosity determined by the Ford glass is & c. Dispersion in translucent light has a Tyndall effect. It is suitable as a primer for applying coatings on resilient materials, in particular textile materials.
    The dispersion dries to obtain a transparent, colorless elastic film, which is characterized by good mechanical properties, hydrolysis resistance and significantly enhanced, compared to known polyurethanes based on aromatic isocyanates, resistance to UV radiation and during heating (for example, 10 minutes at 150 ° C ) does not turn yellow.
    Properties of the obtained film are given in table. one.
    Table 1
    From the table. 1 shows that the residual strength after lOO h irradiation. The xenon lamp was 57 initial values. . PRI m and p 6. Source components: 558 g of polyester based on adipic acid and butanediol (mol. Weight 900); , 5 g. Simple poly7. 97110 ether from V5 weight. % propylene oxide and 85 wt. % ethylene oxide (initiator n-butanol, mol. weight); 29.8 g of propoxylated adduct from 2-butendiol-1, 4 and NaHSO (mol. Weight 25); S 300 g of acetone} 50 g of 4,4-diisocyanatobiphenylmethane; 2 g of butanediol-1, 4, 7 g of acetonazine; 1b90 g deionized water.
    The dehydrated at 120 C mixture from Ote has the effect of Tyndall. polyester, polyether Dispersion suitable for applying para and bisulfite adduct for lowering coatings on resilient materials. It does not viscosity of the obtained prepolymer to obtain a clear, add 300 g of anhydrous acetone. A color elastic film, which then is added, the di-isocyanatodife-15-je is strongly heated (e.g., nilmethane and stirred at 150 ° C for 10 min) does not yellow reaching the NCO value of 6.7. After the polymer is characterized by a higher addition of butanediol, the mixture at the same temperature is allowed to react to obtain an NCO value of 8 wt. % In comparison with the known polyurethylene prepolymer, it is cooled to 20 ° C, acetonazine is added on the basis of aromatic isocyanates, and the amines are resistant to UV irradiation. the reaction between azine and isocyanate. The properties of the obtained film by groups are not observed. With intensive prices in the table. 2.: From the data table. 2 that the residual strength after 00 hours of irradiation with a xenon lamp is about the initial value. EXAMPLE 7- A dispersion according to Example 6 is obtained with the difference that only 920 g of water is used. After distilling off the acetone, the solids content is 55% by weight. % The viscosity of the dispersion determined by the Ford glass is 56 seconds, the dispersion has the effect of Tyndall and can be maintained for 5 months. EXAMPLE 8 A prepolymer was prepared according to Example 6. After cooling to 30 minutes, add a prepolymer.
    melting point (220 ° C), hydrolysis resistant and significantly improved.
    权利要求:
    Claims (2)
    [1]
    Table 2 but stirring is dispersed by adding water. In the resulting dispersion, the acetone content is Juves. The dispersion can be freed from acetone by vacuum distillation, after which the solids content is tO.Bec.,%. The viscosity determined by a Ford glass is 15 seconds. The dispersion in the translucent beetroot A6.1 g of acetohydrazone, while the temperature and viscosity increase somewhat, but without the danger of gelling. Then dispersed as described in example 6. After distilling off the acetone, the solids content is tO weight. % The viscosity determined by the Ford glass is 21 seconds. Dispersion has a translucent light effect of Tyndall. It dries to produce a film, the properties of which correspond to the properties of the product prepared according to example 7. Example 9 (control). A prepolymer according to example 6 is obtained. 99 After cooling, 125 g of the mixture obtained from hydrazine hydrate and acetone are added in a 1: 2 molar ratio. Initially, the mixture is kneaded to a clear appearance, but after some time an exothermic reaction occurs with turbidity and an increase in viscosity. After 5-10 minutes, the product is fully gelated. If dispersed prior to the onset of gelling, a coarse dispersion is obtained without the Tyndall effect, which precipitates on settling. Thus, when carrying out the method, it is necessary to use azines or hydrazones free from water. EXAMPLE 10 Baseline: 400 g of phthalic acid-based polyethyl ester and ethanediol (mol weight 2000); 1050 g of phthalic acid-based polyester, adipic acid and ethanediol (mol. Weight 1750); 85.5 g of polyether from | 15 wt. % propylene oxide and 85 wt. ethylene oxide (initiator n-butanol, mol. weight); 76.6 g of propoxylated adduct from 2-butanediol-1, and NaN503 (mol. Weight 425); 500 g of acetone; 550 g of 4,4-diisocyanatodiphenylmethane; 107.5 g of acetone; 3290 g of de-ionized water. A mixture of both polyesters, polyether and bisulfite adduct, dehydrated at 120 ° C, is diluted with 500 g of anhydrous acetone. Then 4,4-diisocyanatodiphenium methane is added and heated with stirring to 60 ° C to obtain an NCO value of 3.8 weight. %, cooled to 20 ° C and acetonazine is mixed. With vigorous stirring, disperse by adding water. The resulting dispersion contains 8 wt. % acetone, which can be removed by vacuum distillation, and 40 wt. % solids. The viscosity determined by the Ford glass is 15 seconds. Dispersion in translucent light has a Tyndall effect. It dries to form a clear, colorless film and is suitable for application as a coating on paper. Fixture hardness 30 s. The film after 10-minute heating to 150 ° С does not turn yellow. Example 11: Source components: goiter and polyester on 510 ve of adipic acid and butanediol (mol. Weight: 900); 220 g of polyether-based polyether (initiator bisphenol A, mol. Weight 550); 2.7 g of polyether from 15 ppm of propylene oxide and 85 wt. % ethylene oxide (initiator n-butanol, mol. weight); , 5 g of propoxylated adduct from 2-butanediol-1, and NaHSOg (mol. Weight 425); 300 g of acetone; 450 g of 4 / -diisocyanatodiphenylmethane; 3i, g trimethylolpropane; 8.8 g of acetone; 1–50 g of deionized water. 300 g of water-free acetone is added to the viscosity of the resulting prepolymer, which is dehydrated with a mixture of polyester, both polyethers, and a bisulfate adduct. 1,4-Diisocyanatodiphenylmethane is then added and mixed with to obtain NCO. values of 5.8 weight. % After the addition of trimethyl lpropylene at the same temperature, the mixture is allowed to react to obtain an NCO value of k,) weight. % The obtained prepolymer is cooled to, then acetonazine is added and dispersed with vigorous stirring by adding water. The resulting dispersion contains 10 wt. ° / s of acetone, which can be removed by vacuum distillation, after which the solids content is 0 wt. % The viscosity determined by the Ford glass is 18 seconds. Dispersion in translucent light has a Tyndall effect. It dries to a clear, colorless solid film and can be used as an air-drying wood varnish. DETAILED DESCRIPTION A method for producing an aqueous dispersion of polyurethanes by mixing and reacting a prepolymer based on a mixture of polyethers and polyesters and a diol containing chemically bound hydrophilic groups and terminal NCO groups, with an amine type chain extender in the presence of water and an emulsifier, characterized in that in order to increase storage stability, acetonazine or methyl ethyl ketazine or isobutyral 1971105-12 are used as a mine chain extension.
    daein, or acetoni connotation, and in-1. Acceptance for Germany
    The dusts are introduced after mixing prepolymer No. CEBZ, Cl, C 08 G 18/08, published. with extension 1977, Sources of information, s If 558926, cl. C 08 J 3/02, 1975 (taken into account during the examination of the type).
    [2]
    2. USSR author's certificate
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    同族专利:
    公开号 | 公开日
    ES478619A1|1979-06-01|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE19782811148|DE2811148A1|1978-03-15|1978-03-15|PROCESS FOR THE PRODUCTION OF Aqueous POLYURETHANE DISPERSIONS AND SOLUTIONS|
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