Non-inflammable fiber materials and process for producing the same
    3.
    发明授权
    Non-inflammable fiber materials and process for producing the same 失效
    不易燃纤维材料及其制造方法

    公开(公告)号:US4723959A

    公开(公告)日:1988-02-09

    申请号:US795541

    申请日:1985-11-06

    摘要: A non-inflammable fiber material and a process for producing the same are disclosed, said process comprising the steps of:obtaining thready materials, knitted goods, or woven goods, which are composed of a mixed yarn consisting of polymetaphenylene isophthalamide fibers of thermal decomposition temperature not smaller than 350.degree. C. and rayon fibers, or which are composed of 100 weight parts of a mixed yarn consisting of polymetaphenylene isophthalamide fibers of thermal decomposition temperature not smaller than 350.degree. C. and rayon fibers, and from 20 to 100 weight parts of a polymetaphenylene isophthalamide fiber yarn of thermal decomposition temperature not smaller than 350.degree. C., at least said rayon fibers in said thready materials, knitted goods, or woven goods being treated with one or more chemical agents selected from a first chemical agent group consisting of ammonium sulfamate, diammonium imidodisulfonate, ammonium sulfate, ammonium bisulfate, ammonium thiosulfate, ammonium sulfite, and ammonium bisulfite, and one or more chemical agents selected from a second chemical agent group consisting of ammonium dihydrogen phosphate, diammonium hydrogen phosphate, and guanidine phosphate; andheat treating said thready materials, said knitted goods, or said woven goods at from 200 to 260.degree. C. so as to denaturate said rayon fibers in said thready material, said knitted goods, or said woven goods into thermally decomposed heat treated carbonized fibers.

    摘要翻译: 公开了一种不易燃纤维材料及其制造方法,所述方法包括以下步骤:获得由热分解温度的聚对苯二甲酰间苯二胺纤维组成的混合纱线的材料,针织物或编织物 不低于350℃,人造丝纤维,或由100重量份由热分解温度不低于350℃的聚对苯二甲酰间苯二胺纤维和人造丝纤维组成的混合纱线和20-100重量份 的热分解温度不低于350℃的聚邻亚苯基间苯二甲酰胺纤维纱线,至少所述材料中的所述人造丝纤维,针织物或织造物品用一种或多种选自以下的第一化学试剂组 的氨基磺酸铵,亚氨基二磺酸二铵,硫酸铵,硫酸氢铵,硫代硫酸铵,铵 亚硫酸氢铵和亚硫酸氢铵,以及一种或多种选自由磷酸二氢铵,磷酸氢二铵和磷酸胍形成的第二化学剂组的化学试剂; 在200-260℃下对所述材料,所述针织物或所述编织物进行热处理,以将所述材料,所述针织物或所述织造物中的所述人造丝纤维变性为热分解热处理碳化纤维 。

    Organic ammonium sulfite ester compounds and method of preparation
    10.
    发明授权
    Organic ammonium sulfite ester compounds and method of preparation 失效
    有机亚硫酸铵酯化合物及其制备方法

    公开(公告)号:US3168546A

    公开(公告)日:1965-02-02

    申请号:US7913960

    申请日:1960-12-29

    申请人: BAYER AG

    摘要: The invention comprises organic ammonium compounds of formula: where R1 is a hydrocarbon radical, optionally substituted, R2 and R3 are hydrogen or hydrocarbon radicals, optionally substituted, and R4 is an alkylene radical, optionally substituted, and two of the radicals R1, R2 and R3 may be linked to form a heterocyclic ring. R1, R2 and R3 may be substituted with free, esterified or etherified hydroxyl groups or carbocyclic or heterocyclic radicals, and R4 may be substituted with alkyl, hydroxyalkyl or aryl radicals. The compounds may be prepared by reacting an amine with an epoxide and sulphur dioxide, or with an addition product of ethylene oxide and sulphur dioxide, or by reacting a tertiary amine with a glycol sulphite. The reaction may be carried out with or without an inert solvent, e.g. water, dioxane or methylene chloride. In examples compounds are prepared by reacting ethylene oxide and sulphur dioxide with dodecyldimethylamine, dodecylamine and (HO.CH2.CH2.O.CH2.CH2)3N; by reacting the addition product of ethylene oxide and sulphur dioxide with dodecyldimethylamine, cyclohexyldimethylamine, stearylmethylamine, oleyldiethanolamine, triethylamine and products obtained by reacting ethylene oxide with triethanolamine, dimethylethanolamine and stearylmethylamine; by reacting propylene oxide and sulphur dioxide with stearylmethylamine; and by reacting glycol sulphite with dodecyldimethylamine and triethanolamine. A list of amines suitable for preparing the compounds is given including amines, alkanolamines, ethers of alkanolamines, esters of alkanolamines, 2-(dimethylaminomethylene)-tetrahydrofuran, piperidine, N-methylpiperidine and N-methylmorpholine. Other epoxides mentioned are glycide and styrene oxide.ALSO:Organic ammonium compounds which may be used as the reducing component in the redox system in the polymerization of unsaturated compounds, have the formula: where R1 is a hydrocarbon radical, optionally substituted, R2 and R3 are hydrogen or hydrocarbon radicals, optionally substituted, and R4 is an alkylene radical, optionally substituted, and two of the radicals R1, R2 and R3 may be linked to form a heterocyclic ring. R1, R2 and R3 may be substituted with free, esterified or etherified hydroxyl groups or carbocyclic or heterocyclic radicals, and R4 may be substituted with alkyl, hydroxyalkyl or aryl radicals. In the polymerization of acrylonitrile an aqueous solution of a compound of the above formula is added to a mixture of acrylonitrile, acrylic acid methyl ester, water, sulphuric acid and potassium peroxide disulphate, under nitrogen, and the polymerization carried out at 50 DEG C. with shaking.ALSO:The formation of electrostatic charges on synthetic fibres is prevented by contacting with organic ammonium compounds of formula where R1 is a hydrocarbon radical, optionally substituted, R2 and R3 are hydrogen or hydrocarbon radicals, optionally substituted, and R4 is an alkylene radical, optionally substituted, and two of the radicals R1, R2 and R3 may be linked to form a heterocyclic ring. R1, R2 and R3 may be substituted with free, esterified or etherified hydroxyl groups or carbocyclic or heretocyclic radicals, and R4 may be substituted with alkyl, hydroxyalkyl or aryl radicals. Compounds of the above formula are used to spray and impregnate polyamide fibres, based on e -caprolactam, polyacrylonitrile fibres, polyester fibres and polyvinylchloride fibres.