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Manufacture and application of new products useful as assisting agents in the textile and leather industries

机译:新产品的制造和应用,可用作纺织和皮革行业的助剂

摘要

Products stated to have emulsifying properties are obtained by sulphonating cyclic amidines which are derived from o or peri diamines of the benzene or naphthalene series, and which are substituted in the m -position by an aliphatic residue containing at least three carbon atoms or a hydroaromatic residue. Before sulphonation the cyclic amidines may if desired be subjected to alkylation, aralkylation or arylation. In a further modification the same products are obtained by condensing a sulphonic acid of an o-or peri-diamine, in which one amino group may be substituted by an alkyl, aralkyl or aryl group, with an acidylating agent capable of introducing the residue of an aliphatic carboxylic acid containing at least four carbon atoms or the residue of a hydroaromatic carboxylic acid. The cyclic amidines are obtainable by condensing aliphatic carboxylic acids containing at least four carbon atoms, e.g. butyric, caproic, caprylic, capric, arachic, cerotic and naphthenic acids with o- or peri-arylenediamines. The following diamines are mentioned: o-toluylenediamine, chlorinated o-phenylenediamines, o-aminodiphenylamines and o-aminomonomethylaniline. o-Nitroamines may also be used as starting materials. For the alkylation, arylation or aralkylation, chlormethylnaphthalene, alkylhalides, halogenalkylsulphonic acids, chlorhydrins, epichlorhydrins, alkylsulphates and dichlornitrobenzene may be used. In examples, the following imidazoles and perimidines are sulphonated: m -heptadecylbenzimidazole, m - undecylbenzimidazole, m -naphthenylbenzimidazole, m - heptadecyl - N - phenylbenzimidazole, m - heptadecyl - N - benzyl benzimidazole, m - heptadecyl - 1 : 2 - naphthimidazole, m - heptadecylperimidine, m -undecylperimidine and the imidazoles or perimidines obtained from oleic acid or the fatty acids of coconut oil, palm oil, hard fat, soya oil, earthnut oil or bone fat. In a further example, the sodium sulphonates of the mixture of imidazoles obtained from o-phenylenediamine and a mixture of stearic and palmitic acids are added to molten grain soap.ALSO:Products stated to have wetting, softening, emulsifying, levelling, washing, and similar properties are obtained by sulphonating cyclic amidines which are derived from o or peri diamines of the benzene or naphthalene series, and which are substituted in the m -position by an aliphatic residue containing at least three carbon atoms or a hydroaromatic residue. Before sulphonation the cyclic amidines may if desired be subjected to alkylation, aralkylation or arylation. In a further modification the same products are obtained by condensing a sulphonic acid of an o- or peri-diamine, in which one amino group may be substituted by an alkyl, aralkyl or aryl group, with an acidylating agent capable of introducing the residue of an aliphatic carboxylic acid containing at least four carbon atoms or the residue of a hydroaromatic carboxylic acid. The products may be used in the leather as well as in the textile industry. The cyclic amidines are obtainable by condensing aliphatic carboxylic acids containing at least four carbon atoms, e.g. butyric, caproic, caprylic, capric, arachic, cerotic and naphthenic acids with o- or peri-arylenediamines. The following diamines are mentioned: o-toluylenediamine, chlorinated o-phenylenediamines, o-aminodiphenylamines and o-aminomonomethylaniline. o-Nitroamines may also be used as starting materials. For the alkylation, arylation or aralkylation, chlormethylnaphthalene, alkylhalides, halogenalkylsulphonic acids, chlorhydrins, epichlorhydrins, alkylsulphates and dichlornitrobenzene may be used. In the following examples, the imidazoles and perimidines are sulphonated with the usual sulphonating agents in some cases with diluents such as tetrachlorethane: (1) m -heptadecylbenzimidazole is sulphonated and neutralised, and if necessary bleached with a hypochlorite, hydrogenperoxide or a permanganate; the product foams readily and may also be used in a soda lye for treating cotton piece goods, and in a bath for wetting woollen yarn: (2) m -undecylbenzimidazole is sulphonated, and the product used for wetting cotton or wool; it may also be added to a mercerising bath for cotton goods containing soda lye and methylcyclohexanol: (3) a m -naphthenylbenzimidazole derived from the mixed naphthenic acids of Baku petroleum is sulphonated: (4) oleic acid and the fatty acids from coconut-oil, palm oil, hard fat, soya oil, earth nut oil and bone fat are used for the preparation of imidazoles or perimidines which are then sulphonated: (5) stearic acid is condensed with o-aminodiphenyl amine and the m -heptadecyl-N-phenylbenzimidazole sulphonated: (6) stearic acid is condensed with N-benzyl-o-phenylenediamine and the m -heptadecyl-N-benzylbenzimidazole sulphonated: (7) m -heptadecyl-1 : 2-naphthimidazole is sulphonated: (8) m -heptadecylperimidine is sulphonated; the neutralised product may be used for washing wool: (9) m -undecylperimidine is sulphonated: (10) m -heptadecylbenzimidazole is treated with benzyl chloride in the presence of sodium acetate, calcium carbonate or sodium carbonate, and the resulting m -heptadecyl-N-benzylbenzimidazole, after purification sulphonated; instead of the benzyl chloride, alkylchloride may be used: (11) o-phenylenediamine is condensed with a mixture of stearic and palmitic acids, the resulting mixture of benzimidazoles treated with benzyl chloride and the product sulphonated: (12) the benzimidazoles derived from oleic acid or the fatty acids of coconut oil or palm oil are benzylated and then sulphonated: (13) the mixture of benzylated benzimidazoles, prepared according to example 11 in the form of their hydrochlorides, is treated first with sodium carbonate and then with benzylchloride whereby the corresponding benzimidazolium chlorides are produced, which are finally sulphonated. In further examples: (14) stearic acid chloride is condensed with 1 : 8-naphthylene diamine-4-sulphonic acid; (15) woollen piece goods, after being washed in hard water are treated in an aqueous bath with sodium m -undecylbenzimidazolesulphonate to facilitate subsequent dyeing: (16) by mixing the sodium sulphonate of the imidazoles obtained from o-phenylenediamine and a mixture of palmitic and stearic acids, with grain soap, the latter may be used with hard water without the precipitation of calcium soaps: (17) cotton yarn is handled in an alkaline solution of 2 : 3-oxynaphthoic acid anilide containing sodium m -heptadecylbenzimidazole sulphonate and then developed with diazotised-4-chlor-2-amino-1 : 11-diphenylether: (18) hides are chrome tanned, neutralised and then handled in a solution containing sodium m -heptadecylbenzimidazolesulphonate; they are finally stretched and dried.
机译:通过磺化由苯或萘系列邻或二胺衍生的环状am而获得具有乳化性能的产品,并在间位被含至少三个碳原子的脂族残基或氢芳族残基取代。在磺化之前,如果需要,可以将环状am进行烷基化,芳烷基化或芳基化。在进一步的改进中,通过缩合邻或二胺的磺酸得到相同的产物,其中一个氨基可以被烷基,芳烷基或芳基取代,并带有能够引入残基的酸化剂。含有至少四个碳原子的脂族羧酸或氢芳族羧酸的残基。环状am可通过缩合至少含四个碳原子的脂族羧酸而获得。丁酸,己酸,辛酸,癸酸,花生酸,蜡酸和环烷酸与邻或二芳基二胺。提及以下二胺:邻甲苯二胺,氯化邻苯二胺,邻氨基二苯胺和邻氨基单甲基苯胺。邻硝基胺也可以用作起始原料。对于烷基化,芳基化或芳烷基化,可以使用氯甲基萘,烷基卤,卤代烷基磺酸,氯代醇,表氯代醇,烷基硫酸根和二氯硝基苯。在实施例中,以下咪唑和哌啶被磺化:间-十七烷基苯并咪唑,m-十一烷基苯并咪唑,m-萘基苯并咪唑,m-庚基-N-苯基苯并咪唑,m-庚基-N-苄基苯并咪唑,m-庚基甲基-1:从油酸或椰子油,棕榈油,硬脂,大豆油,花生油或骨脂的脂肪酸或油酸得到的间-十七癸基亚丙基,间-十一烷基亚丙基和咪唑或亚丙基。在另一个实例中,将由邻苯二胺制得的咪唑混合物与硬脂酸和棕榈酸混合物中的磺酸钠加入熔融谷物皂中。通过磺化衍生自苯或萘系列的邻或二胺的环am而获得类似的性质,所述环am在间位被含至少三个碳原子的脂族残基或氢芳族残基取代。在磺化之前,如果需要,可以将环状am进行烷基化,芳烷基化或芳基化。在进一步的改进中,通过缩合邻或二胺的磺酸(其中一个氨基可以被烷基,芳烷基或芳基取代)与能引入残基的酸化剂缩合,得到相同的产物。含有至少四个碳原子的脂族羧酸或氢芳族羧酸的残基。该产品可用于皮革以及纺织工业。环状am可通过缩合至少含四个碳原子的脂族羧酸而获得。丁酸,己酸,辛酸,癸酸,花生酸,蜡酸和环烷酸与邻或二芳基二胺。提及以下二胺:邻甲苯二胺,氯化邻苯二胺,邻氨基二苯胺和邻氨基单甲基苯胺。邻硝基胺也可以用作起始原料。对于烷基化,芳基化或芳烷基化,可以使用氯甲基萘,烷基卤化物,卤代烷基磺酸,氯醇,表氯醇,烷基硫酸盐和二氯硝基苯。在下列实施例中,在某些情况下用稀释剂如四氯乙烷用常规的磺化剂磺化咪唑和嘧啶:(1)将间-十七烷基苯并咪唑磺化并中和,必要时用次氯酸盐,过氧化氢或高锰酸盐漂白;该产品容易起泡沫,并且还可以用于处理棉片产品的苏打碱液和用于润湿羊毛纱线的浴中:(2)间-十一烷基苯并咪唑被磺化,该产品用于润湿棉花或羊毛;还可将其添加到丝光浴中,以用于含有苏打碱液和甲基环己醇的棉制品:(3)将来自巴库石油公司混合环烷酸的萘萘苯并咪唑磺化:(4)油酸和椰子油中的脂肪酸,棕榈油,硬脂,大豆油,花生油和骨脂用于制备咪唑或perimidine,然后将其磺化:(5)将硬脂酸与邻氨基二苯胺缩合,将间-十七烷基-N-苯基苯并咪唑磺化:(6)硬脂酸为与N-苄基-邻-苯二胺缩合,使间-十七烷基-N-苄基苯并咪唑磺化:(7)间-十七烷基-1:2-萘咪唑被磺化:(8)间-十七烷基哌啶被磺化;中和后的产物可用于洗涤羊毛:(9)将间十一烷基过嘧啶磺化:(10)在乙酸钠,碳酸钙或碳酸钠的存在下,用苄基氯处理间-十七烷基苯并咪唑,并将所得的间-十七烷基-纯化后磺化N-苄基苯并咪唑;可以使用烷基氯化物代替苄基氯:(11)将邻苯二胺与硬脂酸和棕榈酸的混合物缩合,将苯并咪唑经苄基氯处理的混合物和磺化的产物进行缩合:(12)衍生自油酸的苯并咪唑将椰子油或棕榈油的酸或脂肪酸苄基化,然后磺化:(13)首先用碳酸钠然后用苄基氯处理根据实施例11制备的苄基苯并咪唑盐酸盐形式的混合物。产生相应的苯并咪唑氯化物,最后将其磺化。在进一步的实例中:(14)将硬脂酰氯与1:8-萘二甲胺4-磺酸缩合; (15)羊毛件在硬水中洗涤后,在水浴中用间十一烷基苯并咪唑磺酸钠处理,以利于随后的染色:(16)通过混合从邻苯二胺中得到的咪唑的磺酸钠和棕榈酸酯的混合物和硬脂酸与谷物皂一起使用,后者可以与硬水一起使用而不会沉淀钙皂:(17)棉纱在2:3-氧萘甲酸苯胺的碱性溶液中处理,该溶液含有间庚基苯并咪唑磺酸钠,然后用重氮化的4-氯-2-氨基-1:1 1-二苯醚显影:(18)将皮革鞣制铬,中和,然后在含有间-十七烷基苯并咪唑磺酸钠的溶液中处理;他们终于被拉伸和干燥。

著录项

  • 公开/公告号GB403977A

    专利类型

  • 公开/公告日1934-01-01

    原文格式PDF

  • 申请/专利权人 SOCIETY OF CHEMICAL INDUSTRY IN BASLE;

    申请/专利号GB19320015451

  • 发明设计人

    申请日1932-05-31

  • 分类号

  • 国家 GB

  • 入库时间 2022-08-24 06:57:28

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