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A method for dealkalization of poly saccharide xanthate solutions and entalkalisierte poly saccharide xanthogenate

机译:多糖黄原酸酯溶液的脱碱方法和糖化多糖黄原酸酯的方法

摘要

Decausticized viscose is used as a temporary soil binder. It can be used for preparing concrete or as an adjunct to other concrete binders (Example 58). For the method of preparation of the decausticized viscose, see Division C3. U.S.A. Specification 2,705,231 is referred to.ALSO:A decausticized solution of a polysaccharide xanthate is made by subjecting a crude caustic aqueous solution of an alkali xanthate of a film-forming polysaccharide to ion-exchange or ion-retardation or a combination thereof, to remove a substantial proportion of the free caustic therein. Viscose or amylose xanthate may be so treated. A decausticized viscose substantially free of alkali cellulose and free cellulose may be made by contacting an aqueous viscose solution with sufficient cation-exchange material in the hydrogen ion form to neutralize a substantial proportion of the alkali content of the viscose. A decausticized amylose xanthate substantially free of alkali amylose and free amylose may be made by an analogous method. Thus a predetermined amount of cation-exchange material may be mixed with the viscose at ambient temperature until reaction is complete and the cation exchange material is separated by settling or filtration. Alternatively the viscose may be passed through a column containing the cation-exchange material. In further methods the viscose is passed through a column containing either an anion-exchange material in the salt form or an ion-retarding resin, the effluent in either case comprising decausticized viscose having a pH less than 13. Similarly, decausticized amylose xanthate substantially free of alkali amylose and free amylose may be made by passing an aqueous amylose xanthate solution through a column containing an anion-exchange material in the salt form and recovering the effluent comprising decausticized amylose xanthate. In any of the preceding methods, the solution may be partially dealkalized by dialysis prior to the ion-exchange or ion-retardation treatment. Decausticized aqueous solutions of film-forming polysaccharide xanthates so obtained, e.g. of viscose or amylose xanthate, are of pH 4-13 and substantially free of regenerated polysaccharide. Specified products include decausticized viscose of pH 8-13 substantially free of regenerated cellulose and alkalization and xanthation by-products and containing sodium salts in an amount substantially equivalent to the free alkali content of the viscose when initially formed; decausticized viscose of pH 4-8 substantially free of regenerated cellulose and containing xanthic acid groups in excess of 40% of the xanthate content of the viscose; and analogous amylose xanthate products. A wide range of natural and synthetic ion-exchange materials may be used. Preparation of the decausticized viscose is described in Examples 1-4, 6-9 (cation-exchange), 10, 12-14 (anion-exchange), 15 (ion-retardation), 17 (liquid ion-exchanger), 19, 20 (dialysis followed by cation-exchange), 21 (anion-exchange followed by cation-exchange), 22 (cation-exchange followed by anion-exchange), and 23 (mixed-bed ion-exchange). Preparation of the decausticized amylose xanthate is described in Examples 5 (cation-exchange), 11 (anion-exchange), 16 (ion-retardation), and 18 (dialysis followed by cation-exchange). In Example 36, unidentified cellulose derivatives are obtained by treatment of the decausticized viscose with phenyl isocyanate or with adipoyl chloride. In Example 38, cyanoethylation and carbamoethylation of decausticized viscose are disclosed. Example 52 discloses the preparation of ammonium cellulose xanthate and the corresponding lithium and potassium salts by passing decausticized viscose through a cation-exchange resin in the ammonium form. Example 55 discloses etherification and esterification of decausticized viscose with chloracetic acid and adipoyl chloride respectively. Example 40 discloses the preparation of a dispersion comprising a mixture of nylon and graft polymers of nylon and cellulose by treatment of a mixture of decausticized viscose and hexamethylene diamine with adipoylchloride in carbon tetrachloride solution. U.S.A. Specification 2,705,231 is referred to.ALSO:Decausticized viscose is used as a pigment binder in ink formulations for printing on regenerated cellulose. Heat-treatment after printing converts the viscose into regenerated cellulose. In Example 29, a black ink formulation is made from carbon black and decausticized viscose and used to print regenerated cellulose meat casings, which are then cured by heating at 115 DEG C. For the method of preparation of the decausticized viscose, see Division C3. U.S.A. Specification 2,705,231 is referred to.ALSO:Decausticized solutions of polysaccharide xanthates, especially amylose xanthate and viscose, are used as coating materials, subseqquent thermal regeneration thereof yielding amylose or regenerated cellulose. For the method of preparation of the decausticized solutions (see Division C3). Example 24 describes the coating of hemp paper, starch-sized onion skin paper, rayon-hemp paper and wood pulp paper, with decausticized viscose, followed by drying at 80-100 DEG C. or at 180 DEG C. to obtain papers having high dry and wet strengths. Example 26 describes the use of decausticized viscose as an adhesive in seaming flat cellulose impregnated paper to form tubes. In Example 28, decausticized viscose is sprayed over a freshly printed surface of a cellulose casing and dried at 105 DEG C., to prevent smudging and offsetting of the printed matter. Example 39 discloses the use of decausticized viscose as a coating for thermoplastic film to impart adhesivity to regenerated cellulose and so permit heat sealing of the cellulose film to another object. In Example 44, a bast fibre paper is coated with decausticized viscose and regeneration is effected by standing or drying at 100 DEG C. Example 47 discloses the use of a coating of decausticized viscose, reacted with chloracetic acid, as an ultra-violet barrier. Example 48 discloses the coating of cellulose acetate and polyethylene terephthalate films with decausticized viscose to improve printability. Examples 50, 51 and 54 disclose the coating of nylon or "Dacron" (Registered Trade Mark) fibres, wool, silk, and cellulose esters and ethers with decausticized viscose to produce a regenerated cellulose coating. Example 56 discloses the use of decausticized viscose as a binder in the formation of non-woven textiles from glass, nylon, cellulose acetate and "Mylar" (Registered Trade Mark) fibres. Example 57 discloses the use of decausticized viscose as a protective coating for glass. U.S.A. Specification 2,705,231 is referred to.ALSO:Paper and textile materials are treated with decausticized solutions of polysaccharide xanthates, especially amylose xanthate and viscose, thermal regeneration of which yields amylose or regenerated cellulose. For the method of preparation of the decausticized solutions see Division C3. Example 30 discloses the sizing of cotton muslin in decausticized viscose, followed by air drying and force drying at 80 DEG C. Example 38 discloses the use of a decausticized viscose previously subjected to cyanoethylation or carbamoethylation as a water-regain or static-reducing additive on polyester fibres. Example 50 discloses the coating of nylon fibres with decausticized viscose to produce a composite fibre having a regenerated cellulose coating. Example 56 discloses the use of decausticized viscose as a binder in the formation of nonwoven textiles from glass, nylon, cellulose acetate and "Mylar" (Trade Mark) fibres. Example 24 describes the impregnation of hemp paper, starch sized onion-skin paper, rayon-hemp paper, and wood-pulp paper, with decausticized viscose, followed by drying at 80-100 DEG C., or at 180 DEG C., to obtain papers having high dry and wet strengths. Example 27 describes the impregnation of tissue paper with decausticized viscose, or amylose xanthate, the impregnated paper being formed into tubes and regenerated thermally or in an acid bath. Example 45 discloses the use of decausticized viscose in admixture with paper pulp in the formation of paper to promote the exhaustion of basic resins into the paper, and the use of decausticized viscose as a beater additive. Examples 50, 51 and 54 disclose the coating of nylon, "Dacron" (Trade Mark), wool, silk, and cellulose ester and ether fibres with decausticized viscose to produce a regenerated cellulose coating. U.S.A. Specification 2, 705, 231 is referred to.
机译:脱粘的粘胶用作临时的土壤粘合剂。它可用于制备混凝土或作为其他混凝土粘合剂的助剂(实施例58)。有关去碱化粘胶的制备方法,请参见C3部分。参见美国规范2,705,231。ALSO:通过使成膜多糖的碱性黄药的粗苛性碱水溶液经过离子交换或离子延迟或它们的组合进行离子交换而制得多糖黄药的脱碱溶液。其中很大一部分的游离苛性碱。粘胶或直链淀粉黄药可以这样处理。可以通过使粘胶水溶液与足够的氢离子形式的阳离子交换材料接触以中和该粘胶的大部分碱含量来制备基本上不含碱纤维素和游离纤维素的脱碱化粘胶。可以通过类似方法制备基本不含碱直链淀粉和游离直链淀粉的十碱化直链淀粉黄原酸酯。因此,可以在环境温度下将预定量的阳离子交换材料与粘胶混合,直到反应完成并且通过沉降或过滤分离阳离子交换材料。或者,可将粘胶通过含有阳离子交换材料的柱。在其他方法中,使粘胶通过含有盐形式的阴离子交换材料或离子延迟树脂的柱,在两种情况下,流出物均包含pH小于13的脱苛化粘胶。类似地,脱碱的直链淀粉黄原酸酯基本上不含碱性直链淀粉和游离直链淀粉的制备可以通过使直链淀粉黄原酸酯水溶液通过含有盐形式的阴离子交换材料的柱并回收包含脱碱的直链淀粉黄原酸酯的流出物来制备。在任何前述方法中,在离子交换或离子延迟处理之前,可通过透析使溶液部分脱碱。这样获得的成膜多糖黄药的去泡水溶液。粘胶或直链淀粉黄原酸酯的pH为4-13,并且基本上不含再生多糖。特定的产品包括pH 8-13的脱苛化粘胶,基本上不含再生纤维素和碱化及黄嘌呤副产物,且钠盐的含量基本上等于最初形成时的粘胶酶的游离碱含量; pH为4-8的去苛化粘胶,基本不含再生纤维素,并且含有的黄原酸基团超过粘胶黄原酸酯含量的40%;和类似的直链淀粉黄药产品。可以使用各种各样的天然和合成离子交换材料。实施例1-4、6-9(阳离子交换),10、12-14(阴离子交换),15(离子延迟),17(液体离子交换器),19, 20(透析后进行阳离子交换),21(阴离子交换后进行阳离子交换),22(阳离子交换后进行阴离子交换)和23(混合床离子交换)。实施例5(阳离子交换),11(阴离子交换),16(离子缓凝)和18(透析然后阳离子交换)中描述了脱苛化的直链淀粉黄药的制备。在实施例36中,通过用异氰酸苯酯或己二酰氯处理脱胶粘胶而获得未鉴定的纤维素衍生物。在实施例38中,公开了十碱化粘胶的氰基乙基化和氨基甲酸酯化。实施例52公开了通过使去苛化的粘胶通过铵形式的阳离子交换树脂来制备铵纤维素黄药铵和相应的锂和钾盐。实施例55公开了分别用氯乙酸和己二酰氯将苛化粘胶进行醚化和酯化。实施例40公开了通过在四氯化碳溶液中用己二酰氯处理脱粘的粘胶和六亚甲基二胺的混合物来制备包含尼龙以及尼龙和纤维素的接枝聚合物的混合物的分散体。参见美国专利说明书2705231。ALSO:去胶化粘胶用作油墨配方中的颜料粘合剂,用于在再生纤维素上印刷。印刷后的热处理将粘胶转化为再生纤维素。在实施例29中,由炭黑和去苛化的粘胶制成的黑色油墨配方,用于印刷再生的纤维素肉肠衣,然后在115℃加热固化。关于去苛化的粘胶的制备方法,见C3部分。参见美国专利说明书2,705,231.ALSO:多糖黄原酸酯,特别是直链淀粉黄原酸酯和粘胶的脱胶溶液用作涂料随后进行热再生,得到直链淀粉或再生的纤维素。有关去碱溶液的制备方法(请参阅C3部分)。实施例24描述了用去苛化的粘胶涂布麻纸,淀粉大小的洋葱皮纸,人造丝-大麻纸和木浆纸,然后在80-100℃或180℃下干燥以获得具有高粘度的纸。干湿强度。实施例26描述了用去碱化的粘胶作为粘合剂在缝合平纤维素浸渍纸以形成管中的用途。在实施例28中,将脱苛化的粘胶喷雾在纤维素外壳的新印刷的表面上,并在105℃下干燥,以防止印刷物弄脏和偏移。实施例39公开了使用脱碱的粘胶作为热塑性膜的涂层,以赋予再生纤维素以粘附性,从而使纤维素膜热封到另一个物体上。在实施例44中,韧皮纤维纸涂覆有脱苛化的粘胶,并通过在100℃下静置或干燥进行再生。实施例47公开了与氯乙酸反应的脱苛化的粘胶的涂层作为紫外线屏障的用途。实施例48公开了用去碱化的粘胶涂覆乙酸纤维素和聚对苯二甲酸乙二酯薄膜以改善可印刷性。实施例50、51和54公开了用去碱化的粘胶涂覆尼龙或“ Dacron”(注册商标)纤维,羊毛,丝绸和纤维素酯和醚的涂层,以产生再生的纤维素涂层。实施例56公开了在玻璃,尼龙,乙酸纤维素和“ Mylar”(注册商标)纤维形成的非织造织物中使用脱碱的粘胶酶作为粘合剂。实施例57公开了使用脱碱的粘胶作为玻璃的保护涂层。参见美国专利说明书2705231。ALSO:纸和纺织材料用多糖黄药,特别是直链淀粉黄药和粘胶的脱碱溶液处理,其热再生产生直链淀粉或再生的纤维素。有关去碱溶液的制备方法,请参见C3部分。实施例30公开了在脱粘的粘胶中对棉纱进行上浆,然后在80℃下空气干燥和强制干燥。实施例38公开了一种脱粘的粘胶在预先进行氰基乙基化或氨基甲酸酯化后作为去水剂或静电还原剂的用途。聚酯纤维。实施例50公开了用脱苛化的粘胶涂覆尼龙纤维,以生产具有再生纤维素涂层的复合纤维。实施例56公开了在玻璃,尼龙,乙酸纤维素和“ Mylar”(商标)纤维形成的非织造织物中,使用脱碱的粘胶酶作为粘合剂。实施例24描述了用去碱化的粘胶浸渍麻纸,淀粉大小的洋葱皮纸,人造丝-麻纸和木浆纸,然后在80-100℃或180℃下干燥至获得具有高干强度和湿强度的纸张。实施例27描述了用脱苛化的粘胶或直链淀粉黄原酸酯浸渍薄页纸,将浸渍的纸制成管并热或在酸浴中再生。实施例45公开了在纸的形成中将脱碱的粘胶纤维与纸浆混合使用以促进碱性树脂向纸中的消耗,以及脱碱的粘胶纤维作为打浆添加剂的用途。实施例50、51和54公开了用去碱化的粘胶对尼龙,“ Dacron”(商标),羊毛,丝绸和纤维素酯和醚纤维进行的涂层,以产生再生的纤维素涂层。参见美国规范2,705,231。

著录项

  • 公开/公告号DE1468735A1

    专利类型

  • 公开/公告日1969-08-07

    原文格式PDF

  • 申请/专利权人 TEE-PAK INC.;

    申请/专利号DE1963T024117

  • 发明设计人 J. BRIDGEFORDDOUGLAS;

    申请日1963-06-07

  • 分类号C08B9/00;C08B33/02;

  • 国家 DE

  • 入库时间 2022-08-23 12:18:10

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