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Process for increasing the wash fastness of dyed textiles or flexible organic sheet materials

机译:提高染色纺织品或柔性有机片材耐洗牢度的方法

摘要

The wash fastness of dyed textile or flexible organic sheet material is increased by heating said dyed materials with a monomeric poly-(N-alkoxymethyl)amide of a polybasic organic acid (including carbonic acid) or with a monomeric poly-(N-alkoxymethyl)melamine wherein the alkoxy groups comprise from 1 to 5 carbon atoms. In examples: (1) cotton fabric dyed with Pontamine blue, 1-(p-aminobenzoylamino)-2-methyl - 4 - aminobenzene sQ m-aminobenzoyl-J-acid (2 mols), N.N1-bis(p-aminobenzoyl)-2-sulpho-p-phenylenediamine sQ 1-(m-aminophenyl) - 3 - methyl - 5 - pyrazolone (2 mols) or 1.3 - di - (p - aminophenoxy)propane sQ m - aminobenzoyl-J-acid (2 mols) is impregnated with an aqueous solution of N.N1-bis(methoxymethyl)adipamide, wrung out and heated to 125 DEG C.; by way of contrast the untreated dyeings and dyeings aftertreated with dimethyloladipamide are described; (2) viscose yarn which has been rendered basic by incorporation of a protein or albuminous material and dyed with 1 - amino - 4 - (p - toluidino) - anthraquinone-2.8-disulphonic acid is steeped in a solution of N.N1-bis(methoxymethyl) urea containing ammonium chloride and acetic acid, dried and baked at 160 DEG C.; an aqueous solution of N.N1-bis(methoxymethyl) adipamide containing acetic acid can be used similarly; (3) bleached cotton muslin dyed with Pontamine blue is impregnated with aqueous solutions of N.N1-bis(methoxymethyl)-succinamide, -fumaramide or -sebacamide containing sufficient acetic acid to give a pH of 2.5, dried and ironed; (4) cotton fabrics dyed with Pontamine blue are impregnated with aqueous solutions of N.N1. N11-tris (methoxymethyl) melamine adjusted to various pH values with acetic acid, dried and heated to various temperatures; by way of contrast dyeings aftertreated with di- and trimethylolmelamines are described; (5) bleached cotton muslin dyed with Pontamine blue is impregnated with aqueous alcoholic solutions of N.N1.N11-tris(ethoxymethyl) melamine adjusted to various pH values by acetic acid or sodium acetate, dried and ironed; (6) bleached cotton muslin dyed with Pontamine blue is treated at raised temperature in an aqueous solution containing N.N1.N11 - tris(methoxy - methyl) melamine, sodium chloride and formic acid and dried; analogous treatments with melamine-formaldehyde condensation products are referred to; (7) bleached cotton muslin dyed with dianisidine sQ 1-amino-8-naph - thol-2.4-disulphonic acid (2 mols) (coppered), p-phenylenediamine (2 mols) sQ di-J-acid, 3.31 - diaminoazoxybenzene sQ J - acid (2 mols) or m-aminobenzoyl-p-toluylenediamine sQ N-(m-aminobenzoyl)-J-acid (2 mols) is impregnated with an aqueous solution of N.N1.N11 - tris(methoxymethyl)melamine containing acetic acid, dried and baked at 164 DEG C.; (8) viscose fabric dyed with p-phenylenediamine -- 1-naphthylamine-6-sulphonic acid -- 2-amino-7-naphthol-3-sulphonic acid -- 1-naphthylamine-6-sulphonic acid or aniline -- urea-J-acid sM p-aminoacetanilide are impregnated with an aqueous solution of N.N1.N11 - tris(methoxymethyl)melamine containing acetic acid, dried and baked at 165 DEG C.; (9) cellulose acetate or nylon fabric dyed with p-aminoacetanilide -- p-cresol or p-nitraniline -- aniline is treated as in (8); (10) woven wool or leather dyed with p-phenylenediamine -- 1.8-dihydroxynaphthalene-3.6-disulphonic acid or phenol sM benzidine -- 2 - naphthylamine - 3.6 - disulphonic acid (p - toluene sulphonated) is treated as in (8). Additional aftertreatment agents specified are N.N1 - bis(butoxymethyl)adipamide, N.N1.N11-tris(methoxymethyl)tricarballylamide and N.N1-bis(isopropoxymethyl)urea. The process is applicable to all types of dyeings, those effected with acid, direct, basic, pigment, sulphur and vat dyestuffs being specified. These dyestuffs may be azo, anthraquinone, indigo, thioindigo, azine, oxazine, azomethine, nitro, stilbene or triphenylmethane dyestuffs. Specified materials which may be treated are wood pulp, cotton, linen, ramie, hemp, jute, wool, silk, hair and fibres derived from nylons, vinyl polymers, casein, zein, soya protein, cellulose esters and ethers and regenerated cellulose. Solvents useful for the aftertreatment agents are water and alkanols of one to four carbon atoms and their ethers. Wetting, softening and swelling agents may be added to the solutions. Acidic catalysts can be employed before, during or after the impregnation and may be applied as vapours. Substances which become acidic during the heating stage may be employed, e.g. ammonium chloride or acetate. Specifications 486,577, 503,168, 537,971, 557,932 and 567,063 are referred to. The Specification as open to inspection under Sect. 91 comprises also heating dyed materials with any monomeric ether of a poly-(N-methylol) compound. By way of contrast with example (5) above dyeings aftertreated with an alcoholic or dimethyformamide solution of a condensation product from melamine and formaldehyde in absolute ethanol in presence of hydrochloric acid, are described. In a further example, cotton cloth dyed with Pontamine blue is impregnated with an aqueous solution of N.N1-bis(methoxymethyl)uron, N.N1-bis(methoxymethyl)ethyleneurea (prepared from dimethylolethyleneurea and methanol), 1.3-bis-(methoxymethyl)-5-methyl-s-triazone or N.N1-bis(methoxymethyl) - 5.5 - dimethylhydantoin (prepared from 5.5-dimethylhydantoin, formaldehyde and methanol) containing acetic acid and baked at 125 DEG C. In example (7) above the cotton may be dyed with a sulphonated copper phthalocyanine. The poly-(N-methylol) compounds may be derived from carbonamides, oxoamides, thioamides, amidines, guanidines, cyclic amides, cyclic amidines, cyclic ureas, sulphonamides and phosphonamides. Further compounds specified are: N.N1-bis(phenoxymethyl)adipamide, N.N1 - bis(a - naphthoxy - methyl)urea, N.N1.N11 - tris(cyclohexyl - or allyl - oxymethyl) melamine, N.N1.N11.N111 - tetrakis(methoxymethyl)methylenediurea, N. N1 - bis(methoxymethyl) - biuret, - adipic di - hydrazide, p - dicyandiamide, - terephthalamide, - hydantion, -adipohydroxamic acid, -guani - dine, -diketopiperazine, - pyrrolidinedicarbon - amide or -dithioxamide, N.N1 - bis(benzyloxymethyl)urea, N.N1-bis(ethoxymethyl)-thiourea or -uracil and N.N1.N11-tris(methoxymethyl)-phenybiguanide or -cyanuric acid. These are prepared from the methylol compounds and alcohols in the presence of an acidic catalyst. Dyestuff intermediates, e.g. coupling components, diazotisation components and compound which form colours by condensation reactions, may also be fixed upon materials by the process. This subject-matter does not appear in the Specification as accepted.
机译:通过将染色材料与多元有机酸(包括碳酸)的单体聚(N-烷氧基甲基)酰胺或单体聚(N-烷氧基甲基)一起加热,可提高染色织物或柔性有机片材的耐洗牢度。其中烷氧基包含1至5个碳原子的三聚氰胺。在实例中:(1)用Pont胺蓝,1-(对氨基苯甲酰基氨基)-2-甲基-4-氨基苯 sQ间氨基苯甲酰基-J-酸(2 mols),N.N1-双(p-氨基苯甲酰基)-2-磺基对苯二胺 sQ 1-(间氨基苯基)-3-甲基-5-吡唑啉酮(2 mols)或1.3-二-(对氨基苯氧基)丙烷 sQ m-氨基苯甲酰基-J-用N.N1-双(甲氧基甲基)己二酰胺水溶液浸渍酸(2摩尔),将其拧干并加热至125℃。相比之下,描述了未处理的染料和用二甲基奥糖酰胺处理的染料。 (2)将通过掺入蛋白质或白蛋白而变成碱性并用1-氨基-4-(对甲苯基)-蒽醌-2.8-二磺酸染色的粘胶纱浸渍在N.N1-bis溶液中将含有氯化铵和乙酸的(甲氧基甲基)脲干燥并在160℃下烘烤;类似地,可以使用含有乙酸的N.N1-双(甲氧基甲基)己二酰胺的水溶液。 (3)用含有足够的乙酸使pH值为2.5的N.N1-双(甲氧基甲基)-琥珀酰胺,-富马酰胺或-癸二酰胺的水溶液浸透用庞他敏蓝染色的漂白棉薄纱,干燥并熨烫; (4)用N.N1的水溶液浸渍用庞塔明蓝染色的棉织物。将N11-三(甲氧基甲基)三聚氰胺用乙酸调节至各种pH值,干燥并加热至各种温度;作为对比,描述了用二羟甲基蜜胺和三羟甲基蜜胺处理的染料。 (5)将用蓬塔明蓝染色的漂白棉薄纱浸以N.N1.N11-三(乙氧基甲基)三聚氰胺的乙醇溶液,用乙酸或乙酸钠调节至各种pH值,干燥并熨烫; (6)在升高的温度下在含有N.N1.N11-三(甲氧基-甲基)三聚氰胺,氯化钠和甲酸的水溶液中处理用蓬塔明蓝染色的漂白棉平纹细布,并干燥;涉及三聚氰胺-甲醛缩合产物的类似处理; (7)漂白的棉签,用二苯并核苷 sQ 1-氨基-8-萘酚-thol-2.4-二磺酸(2 mols),对苯二胺(2 mols) sQ二-J-酸3.31-染色用N.N1.N11-tris(N.N11.N11)水溶液浸渍N-(间氨基苯甲酰基)-J-酸(2摩尔)或N-(间氨基苯甲酰基)-J-酸(2摩尔)含乙酸的甲氧基甲基)三聚氰胺,干燥并在164℃下烘烤; (8)用对苯二胺染色的粘胶织物-> 1-萘胺-6-磺酸-> 2-氨基-7-萘酚-3-磺酸-> 1-萘胺-6-磺酸或苯胺- ->用N.N1.N11-含乙酸的三(甲氧基甲基)三聚氰胺的水溶液浸渍尿素-J-酸 sM对氨基乙酰苯胺,干燥并在165℃下烘烤; (9)按(8)处理用对氨基乙酰苯胺->对甲酚或对硝基苯胺->苯胺染色的醋酸纤维素或尼龙织物; (10)用对苯二胺染色的机织羊毛或皮革-> 1.8-二羟基萘-3.6-二磺酸或苯酚 sM联苯胺-> 2-萘胺-3.6-二磺酸(对甲苯磺化)按( 8)。指定的其他后处理剂是N.N1-双(丁氧基甲基)己二酰胺,N.N1.N11-三(甲氧基甲基)三碳烯丙基酰胺和N.N1-双(异丙氧基甲基)脲。该方法适用于所有类型的染色,其中规定了使用酸,直接,碱性,颜料,硫和还原染料进行的染色。这些染料可以是偶氮,蒽醌,靛蓝,硫靛蓝、,嗪,恶嗪,偶氮甲碱,硝基、,或三苯甲烷染料。可以处理的特定材料是木浆,棉,亚麻、,麻,大麻,黄麻,羊毛,丝绸,毛发和源自尼龙,乙烯基聚合物,酪蛋白,玉米蛋白,大豆蛋白,纤维素酯和醚以及再生纤维素的纤维。对于后处理剂有用的溶剂是水和具有1-4个碳原子的链烷醇及其醚。可以将润湿剂,软化剂和溶胀剂添加到溶液中。可以在浸渍之前,之中或之后使用酸性催化剂,并且可以将其用作蒸气。可以使用在加热阶段变成酸性的物质,例如。氯化铵或醋酸铵。规格486,577、503,168、537,971、557,932和567,063。该规范可供本节检查。 91还包括将染色的材料与聚(N-羟甲基)化合物的任何单体醚一起加热。通过与上述实施例(5)的对比,描述了在盐酸存在下用三聚氰胺和甲醛的缩合产物的醇或二甲基甲酰胺溶液在无水乙醇中的后处理染料。在另一实例中,用N.N1-双(甲氧基甲基)脲,N.N1-双(甲氧基甲基)亚乙基脲(由二羟甲基亚乙基脲和甲醇制备),1.3-双-(含乙酸的N.N1-双(甲氧基甲基)-N-N1-双(甲氧基甲基)-5.5-二甲基乙内酰脲(由5.5-二甲基乙内酰脲,甲醛和甲醇制得)并在125℃下烘烤。在上述实施例(7)中棉可以用磺化酞菁铜染色。聚(N-羟甲基)化合物可以衍生自碳酰胺,氧代酰胺,硫代酰胺,am,胍,环酰胺,环am,环脲,磺酰胺和膦酰胺。所指定的其他化合物是:N.N1-双(苯氧基甲基)己二酰胺,N.N1-双(α-萘氧基-甲基)脲,N.N1.N11-三(环己基-或烯丙基-氧甲基)三聚氰胺,N.N1。 N11.N111-四(甲氧基甲基)亚甲基二脲,N. N1-双(甲氧基甲基)-缩二脲,-己二酸二酰肼,对-双氰胺,-对苯二甲酰胺,-酰化,-己二羟肟酸,-胍基-丁,-二酮哌嗪,-吡咯烷二碳-酰胺或-二硫代乙酰胺,N.N1-双(苄氧基甲基)-脲,N.N1-双(乙氧基甲基)-硫脲或-尿嘧啶和N.N1-N11-三(甲氧基甲基)-苯并双胍或-氰尿酸。这些是在酸性催化剂存在下由羟甲基化合物和醇制备的。染料中间体,例如通过缩合反应形成颜色的偶合组分,重氮化组分和化合物也可以通过该方法固定在材料上。该主题未在接受的规范中出现。

著录项

  • 公开/公告号GB573790A

    专利类型

  • 公开/公告日1945-12-06

    原文格式PDF

  • 申请/专利权人 E. I. DU PONT DE NEMOURS AND CO.;

    申请/专利号GB19430014743

  • 发明设计人

    申请日1943-09-08

  • 分类号C09B35/22;C09B35/28;C09B35/56;D06P1/642;D06P1/649;

  • 国家 GB

  • 入库时间 2022-08-24 03:04:13

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