4.
    发明专利
    未知

    公开(公告)号:AT271376B

    公开(公告)日:1969-05-27

    申请号:AT1090866

    申请日:1966-11-25

    Applicant: BASF AG

    Abstract: 1,141,515. Mixed aminoplast textile treating compositions. BADISCHE ANILIN- & SODAFABRIK A.G. 25 Nov., 1966 [27 Nov., 1965; 8 June, 1966], No. 52871/66. Heading C3R. [Also in Division D1] A composition suitable for use in the treatment of cellulosic fabrics comprises (a) at least one poly-N-methylol compound which condenses at a temperature less than 140‹ C., (b) at least one poly-N-methylol compound which condenses at a temperature of at least 140‹ C. and (c) at least one acid curing catalyst which forms an acid under the conditions of condensation. The poly-N-methylol compounds contain two or more hydroxymethyl or alkoxymethyl groups having 1-5 carbon atoms in the alkoxy group which are attached to nitrogen. The compounds (a) may have the formula in which each R 1 is a hydrogen atom or when taken together the two substituents R 1 denote and the substituents R 2 which may be the same or different are hydrogen atoms or alkyl groups having 1-4 carbon atoms and the compounds (b) may have the formula or in which R 3 is a hydrogen atom or alkyl group having 1-4 carbon atoms, R 4 is R 5 is a hydrogen atom, an alkyl group having 1-4 carbon atoms or a group of the formula R 3 O-CH 2 -, R 6 is an alkylene group having 2-4 carbon atoms, R 7 is methyl or ethyl and n is 0 or 1, the compounds containing at least two R 3 O-CH 2 - groups. The acid curing catalyst may be aluminium sulphate, zinc chloride, zinc nitrate, ammonium chloride, ammonium nitrate, ammonium phosphate and salts of ethanolamine, diethanolamine, 2- hydroxy - 2 - methylpropylamine with hydrochloric acid, magnesium chloride and magnesium sulphate. The compounds (a), (b) and (c) may be applied to the fabrics from an aqueous bath which may also contain wetting agents, e.g. salts of alkylnaphthalene sulphonic acids, alkali metal salts of sulphonated dioctyl succinate and adducts of alkylene oxides with fatty alcohols, alkyl phenols or fatty amines, water repelling agents, e.g. paraffin wax emulsions containing aluminium or zirconium, silicon containing formulations and perfluorinated aliphatic compounds, softeners, e.g. ethenoxylation products of high molecular weight fatty acids, fatty alcohols or fatty amides, high molecular weight polyglycol ethers and esters thereof, high molecular weight fatty acids, fatty alcohol sulphonates, stearyl-N,N-ethyleneurea and stearylamidomethyl pyridimium chloride, finishes, e.g. cellulose ethers and esters, alginates, polyamides, ether-oxylated polyamides, polyvinyl ethers, polyvinyl alcohol, polyacrylic or methacrylic acid or esters or amides thereof, polyvinyl propionate, polyvinyl pyrrolidone, copolymers of vinyl chloride and acrylic esters, butadiene and styrene or acrylonitrile, α-dichloroethylene, #-chloroalkyl acrylic esters or vinyl-#-chloroethyl ether and acrylamide or amides of crotonic or maleic acid, or N-methylolmethacrylamide and other polymerizable compounds, or polyethylene, and optical brighteners. In examples the aminoplast mixtures are: dimethylol ethyleneurea plus (1) dimethylol glyoxal monoureine or (2) dimethylol ethyl - urethane or (4) dimethylol urea and dimethylol glyoxal monoureine; or (3) dimethylol propyleneurea plus dimethylol 4-methoxy-5: 5- dimethylpropyleneurea; or (5) dimethylol glyoxal monoureine plus dimethylol 5-isobutyl hexahydro - 1: 3: 5 - triazinone - 2. These are used in aqueous solution containing MgCl 2 or Mg(SO 4 ) 2 and optionally polyethylene emulsion and/or a copolymer of butyl acrylate/butylene diacrylate / methylol methacrylamide / acrylamide and optionally ethoxylated iso-octylphenol.

    6.
    发明专利
    未知

    公开(公告)号:DE2210283A1

    公开(公告)日:1973-09-20

    申请号:DE2210283

    申请日:1972-03-03

    Applicant: BASF AG

    Abstract: 1415206 Textile-treating urea-formaldehydeglyoxal resins BADISCHE ANILIN- & SODAFABRIK AG 2 March 1973 [3 March 1972] 10214/73 Headings C3R and C3P [Also in Divisions D1-D2] A textile-treating resin is obtained by condensing urea with formaldehyde in a 1 : 2-10 molar ratio in aqueous solution at pH 7-10 and 20-80‹ C. for 0À5-4 hours, then at pH 31-5 and 20-100‹ C. until 5 drops of the solution produce turbidity in 10 ml. of 50% aqueous MgSO 4 .7H 2 O, then adding urea, glyoxal and optionally formaldehyde and heating at pH 5-7 and 20-60‹ C. for 1-6 hours, the final molar ratio of urea : formaldehyde : glyoxal being 1 : 1À5-2À5 : 0À3-0À6. In Examples 1-4 initial condensates of U : F ratio 1 : 4 are acidified with H 2 SO 4 or H.COOH to pH 3À5 to 4À8, heated at 35-90‹ C. for 20 mins to 4 hours and neutralized with NaOH; urea and glyoxal (and in Ex. 4 formalin) are added and the mixture heated at 50-55‹ C. for 3-4 hours; the U : F : G ratios of the products are 1 : 2-2À24 : 0À4-0À5. In Examples 5-7 cotton fabrics are treated with aqueous compositions containing the product of Ex. 2 or 3 and MgCl 2 alone or with a polyethylene emulsion or polyvinyl acetate/ starch mixture.

    Crease-resistant finish on cellulose fibres

    公开(公告)号:DE1946290A1

    公开(公告)日:1971-03-25

    申请号:DE1946290

    申请日:1969-09-12

    Applicant: BASF AG

    Abstract: The finish is obtained by (1) reacting the cellulose with an acrylic acid N-methylolamide in (i) a first step, in the presence of 1 acetalisation catalysts and (ii) a second step, in the swollen state, in the presence of an alkaline catalyst, and then (2) treating the fibrous material with a bath containing an aqueous peroxide. The fibrous material has very good crease-recovery properties in both wet and dry state. The process leads to good Monsanto values and no yellowing. Loss of strength, especially after treatment with chlorine, is relatively low.

    8.
    发明专利
    未知

    公开(公告)号:AT264457B

    公开(公告)日:1968-09-10

    申请号:AT520466

    申请日:1966-06-01

    Applicant: BASF AG

    Abstract: A composition suitable for use in the treatment of textiles comprises an aqueous dispersion containing (a) a polyamide which is a co-condensate of 25-40% by weight of one or more lactams having 6-12 carbon atoms in the lactam ring or of equivalent omega-aminocarboxylic acids, 25-40% by weight of one or more salts of hexamethylene diamine with linear dicarboxylic acids having 6-12 carbon atoms, 25-40% by weight of one or more salts of 4,41-diamino-dicyclohexylmethane with linear dicarboxylic acids having 6-12 carbon atoms and 0-10% by weight of one or more other polyamide-forming substances and (b) a protective colloid which is a water-soluble copolymer having a K value of at least 90 and derived from 10-35% by weight of acrylic and/or methacrylic acid, 57.5-90% by weight of a mixture consisting of acrylamide and 5-40% by weight (on the whole of the monomers) of methacrylamide and 0-7.5% by weight of one or more other monomers. Suitable other polyamide-forming substances are dicarboxylic acids, omega-aminocarboxylic acids or diamines which are branched or contain a hetero atom in the chain, and C-substituted lactams. The other monomers in the protective colloid may be a -chloro-acrylic, phenylacrylic, crotonic, maleic, fumaric, itaconic, citraconic, mesaconic or vinylsulphonic acid or an anhydride, salt or ester thereof, methyl or ethyl acrylate or methacrylate, vinyl acetamide, N-dimethylacrylamide, N-methylacrylamide, N-ethylacrylamide or a vinyl lactam. Particularly preferred protective colloids contain 0.005-1% by weight of copolymerizable monomers containing N-methylol groups, e.g. derivatives of urea, melamine, dicyandiamide and guanidine containing N-methylol groups and groups with polymerizable olefinic double bonds and particularly N-methylolmethacrylamide and N-methylolacrylamide. The dispersion may contain 0.5-5% by weight of the protective colloid based on the weight of the polyamide. The dispersions may be prepared by mixing a solution of the polyamide in an organic solvent, e.g. ethanol, isopropanol, butanol or a mixture thereof, with water which contains the protective colloid and, if desired, distilling off all or part of the solvent. The dispersion may also contain polyolefines, polyacrylates, water repellents, dyes, pigments, thickening agents, organic solvents and reaction products, which may be etherified with alcohols containing up to four carbon atoms, of formaldehyde with urea, melamine, ethyleneurea, trimethyleneurea, 4,5-dihydroxy imidazolidone-(2), triazone (2) and its 5-alkyl and 5-hydroxy-alkyl derivatives having up to four carbon atoms in the alkyl or hydroxyl alkyl radical, 5-hydroxytrimethyleneurea or urones. In one example, the dispersion also includes an acrylonitrile-methyl acrylate (50/50) copolymer which has been incompletely hydrolysed with ammonia.ALSO:Fabrics e.g. of cotton, are coated with an aqueous dispersion containing (a) a polyamide which is a cocondensate of 25-40% by weight of one or more lactams having 6-12 carbon atoms in the lactam ring or of equivalent omega-aminocarboxylic acids, 25-40% by weight of one or more salts of hexamethylene diamine with linear dicarboxylic acids having 6-12 carbon atoms, 25-40% by weight of one or more salts of 4, 41-diaminodicyclohexylmethane with linear dicarboxylic acids having 6-12 carbon atoms and 0-10% by weight of one or more other polyamide-forming substances and (b) a protective colloid which is a water-soluble copolymer having a K value of at least 90 and derived from 10-35% by weight of acrylic and/or methacrylic acid, 57.5-90% by weight of a mixture consisting of acrylamide and 5-40% by weight (on the whole of the monomers) of methacrylamide and 0-7.5% by weight of one or more other monomers, and then dried and heated to at least 100 DEG C. Suitable other polyamide-forming substances are dicarboxylic acids, omega-aminocarboxylic acids or diamines which are branched or contain a hetero atom in the chain, and C-substituted lactams. The other monomers in the protective colloid may be a -chloro-acrylic, phenylacrylic, crotonic, maleic, fumaric, itaconic, citraconic, mesaconic or vinylsulphonic acid or an anhydride, salt or ester thereof, methyl or ethyl acrylate or methacrylate, vinyl acetamide, N-dimethylacrylamide, N-methyl acrylamide, N-ethyl-acrylamide or a vinyl lactam. Particularly preferred protective colloids contain 0.005-1% by weight of copolymerizable monomers containing N-methylol groups, e.g. derivatives of urea, melamine dicyandiamide and guanidine containing N-methylol groups, and groups with polymerizable olefinic double bonds and particularly N-methylolmethacrylamide and N-methylolacrylamide. The dispersion may contain 0.5-5% by weight of the protective colloid based on the weight of the polyamide. The dispersions may be prepared by mixing a solution of the polyamide in an organic solvent, e.g. ethanol, isopropanol, butanol or a mixture thereof, with water which contains the protective colloid and if desired distilling off all or part of the solvent. The dispersion may also contain polyolefines, poly-acrylates, water repellents, dyes, pigments, thickening agents, organic solvents and reaction products, which may be etherified with alcohols containing up to four carbon atoms, of formaldehyde with urea, melamine, ethyleneurea, trimethyleneurea, 4, 5-dihydroxy imidazolidone-(2), triazone (2) and its 5-alkyl and 5-hydroxyalkyl derivatives having up to four carbon atoms in the alkyl or hydroxyl alkyl radical, 5-hydroxytrimethyl-eneurea or uranes.ALSO:Textile material, e.g. cotton fabric, is finished and non-woven fabrics bonded by treating them with an aqueous dispersion containing (a) a polyamide which is a cocondencate of 25-40% by weight of one or more lactams having 6-12 carbon atoms in the lactam ring or of equivalent omega-aminocarboxylic acids, 25-40% by weight of one or more salts of hexamethylene diamine with linear dicarboxylic acids having 6-12 carbon atoms, 25-40% by weight of one or more salts of 4, 41-diaminodicyclohexylmethane with linear dicarboxylic acids having 6-12 carbon atoms and 0-10% by weight of one or more other polyamide-forming substances and (b) a protective colloid which is a water-soluble copolymer having a K value of at least 90 and derived from 10-35% by weight of acrylic and/or methacrylic acid, 57.5-90% by weight of a mixture consisting of acrylamide and 5-40% by weight (on the whole of the monomers) of methacrylamide and 0-7.5% by weight of one or more other monomers, and then drying and heating the treated material to at least 100 DEG C. Suitable other polyamide-forming substances are dicarboxylic acids, omega-aminocarboxylic acids or diamines which are branched or contain a hetero atom in the chain, and C-substituted lactams. The other monomers in the protective colloid may be a -chloro-acrylic, phenylacrylic, crotonic, maleic, fumaric, itaconic, citraconic, mesaconic or vinylsulphonic acid or an anhydride, salt or ester thereof, methyl or ethyl acrylate or methacrylate, vinyl acetamide, N-dimethylacrylamide, N-methyl acrylamide, N-ethylacrylamide or a vinyl lactam. Particularly preferred protective colloids contain 0.005-1% by weight of copolymerizable monomers containing N-methylol groups, e.g. derivatives of urea, melamine, dicyandiamide and guanidine containing N-methylol groups, and groups with polymerizable olefinic double bonds and particularly N-methylolmethacrylamide p and N-methylolacrylamide. The dispersion may contain 0.5-5% by weight of the protective colloid based on the weight of the polyamide. The dispersions may be prepared by mixing a solution of the polyamide in an organic solvent, e.g. ethanol, isopropanol, butanol or a mixture thereof, with water which contains the protective colloid and if desired distilling off all or part of the solvent. The dispersion may also contain polyolefines, poly-acrylates, water repellents, dyes, pigments, thickening agents, organic solvents and reaction products, which may be etherified with alcohols containing up to four carbon atoms, of formaldehyde with urea, melamine, ethyleneurea, trimethyleneurea, 4, 5-dihydroxy imidazolidone-(2), triazone-(2) and its 5-alkyl and 5-hydroxyalkyl derivatives having up to four carbon atoms in the alkyl or hydroxyl alkyl radical, 5-hydroxytrimethyleneurea or uronea.

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