Process for preparing a high-molecular-weight polyester
    1.
    发明授权
    Process for preparing a high-molecular-weight polyester 失效
    制备高分子量聚酯的方法

    公开(公告)号:US5439719A

    公开(公告)日:1995-08-08

    申请号:US294922

    申请日:1994-08-24

    Abstract: A high-molecular-weight polyester is to be prepared in such a way that it is possible to very quickly and advantageously obtain even relatively small amounts having a very high molecular weight.This is achieved by preparing a polyester containing proportions of an alkene diol by continuing the polycondensation step until a viscosity number from 5 to 150 cm.sup.3 /g is reached and subsequently subjecting the polyester thus obtained to a treatment with ionizing radiation until the required viscosity number is reached.With the aid of the process of the invention it is possible to obtain high-molecular-weight polyesters having the desired property profile.

    Abstract translation: 高分子量聚酯以这样的方式制备,使得可以非常快速且有利地获得具有非常高分子量的甚至更小的量。 这是通过继续缩聚步骤制备含有比例的烯烃二醇的聚酯来实现的,直到达到5至150cm 3 / g的粘度,然后将所得聚酯经电离辐射处理直到所需粘度数为 到达。 借助于本发明的方法,可获得具有所需性能特征的高分子量聚酯。

    Catalytic system and a process for preparing alpha, omega-C.sub.4
through C.sub.20 alkenols
    3.
    发明授权
    Catalytic system and a process for preparing alpha, omega-C.sub.4 through C.sub.20 alkenols 失效
    催化体系和制备α,ω-C4至C20链烯醇的方法

    公开(公告)号:US4695661A

    公开(公告)日:1987-09-22

    申请号:US841490

    申请日:1986-03-19

    CPC classification number: B01J27/1806 C07C29/60

    Abstract: In order to produce pure alpha, omega-C.sub.4 to C.sub.20 alkenols having purities in excess of 90% by dehydrating the corresponding alpha, omega-C.sub.4 to C.sub.20 diols, a catalyst is used which was prepared by using an alkaline earth orthophosphate or alkaline earth hydrogen phosphate or by reacting an alkaline earth compound with phosphoric acid into the corresponding phosphate and then adding an alkali or alkaline earth compound. This catalyst is suitable to be shaped, next it is dried and then calcined at temperatures between 350.degree. and 950.degree. C. The educt dehydration takes place at temperatures between 300.degree. and 500.degree. C. in selective and partial manner to obtain pure alpha, omega-C.sub.4 to C.sub.20 alkenols at conversions exceeding 90%.

    Abstract translation: 为了通过使相应的α,ω-C4至C20二醇脱水来生产纯度超过90%的纯α,ω-C4至C20链烯醇,使用的催化剂是通过使用碱土金属磷酸盐或碱土氢 或通过使碱土金属化合物与磷酸反应进入相应的磷酸盐,然后加入碱金属或碱土金属化合物。 该催化剂适于成型,然后将其干燥,然后在350℃和950℃之间的温度下煅烧。脱水脱水以选择性和部分方式在300-500℃的温度下进行,以获得纯的α, ω-C4至C20链烯醇,转化率超过90%。

    Process for the preparation of high molecular weight polyesters
    5.
    发明授权
    Process for the preparation of high molecular weight polyesters 失效
    制备高分子量聚酯的方法

    公开(公告)号:US5397529A

    公开(公告)日:1995-03-14

    申请号:US207079

    申请日:1994-03-08

    CPC classification number: C08G63/54

    Abstract: A process for producing high molecular weight polyester is provided which allows the production of small quantities of very high molecular weight polyester in a commercially convenient manner, comprising:polycondensing an aromatic dicarboxylic acid with a mixture of an alkanediol and an alkenediol in the presence of a catalyst and in the substatial absence of oxygen, up to a viscosity number in the range from 50 to 140 cm.sup.3 /g to obtain a polyester,contacting said polyester with 0.001 to 8% by weight of an agent which forms free radicals and dissociates with a half-life of 5 seconds to 120 minutes at temperatures in the range from 130.degree. to 350.degree. C., andreacting said polyester and said agent which forms free radicals to provide the high molecular weight polyester.

    Abstract translation: 提供了一种制备高分子量聚酯的方法,其允许以商业上方便的方式生产少量非常高分子量的聚酯,其包括:在芳族二羧酸与链烯二醇和烯二醇的混合物之间,在 催化剂,并且在不存在氧气的情况下,直到粘度数在50至140cm 3 / g范围内,以获得聚酯,使所述聚酯与0.001至8重量%的形成游离基的试剂接触,并与 在130-350℃的温度下半衰期为5秒至120分钟,并使所述聚酯和形成自由基的所述试剂反应以提供高分子量聚酯。

    Method for processing substituted 1,3-diols of low water solubility
    6.
    发明授权
    Method for processing substituted 1,3-diols of low water solubility 失效
    处理低水溶性的取代1,3-二醇的方法

    公开(公告)号:US4665241A

    公开(公告)日:1987-05-12

    申请号:US861760

    申请日:1986-05-09

    Inventor: Walter K. Homann

    CPC classification number: C07C29/136 C07C29/86

    Abstract: Crude product substituted 1,3-diols obtained by aldolization and subsequent hydrogenation are treated at elevated temperatures with at least sufficient basic additives to reduce the saponification number to zero. Thereupon, the saponified product is reacted with 5 to 30% water and possibly cooled to 1.degree. to 30.degree. C. The aqueous phase is separated mechanically, and following the separation and addition of 5 to 30% water the organic phase is adjusted to a pH of 8.0 to 10.5. A second aqueous phase is removed and, thereupon, the monovalent alcohol is removed by distillation from the second organic phase. Again the pH value of the second organic phase is set at 8.0 to 10.5 and the 1,3-diol is recovered by fractionation.

    Abstract translation: 通过醛醇缩合和随后氢化获得的粗产物取代的1,3-二醇在高温下用至少足够的碱性添加剂进行处理,以将皂化值减少至零。 因此,皂化产物与5至30%的水反应并可能冷却至1至30℃。将水相机械分离,并且在分离并加入5至30%的水后,将有机相调节至 pH为8.0〜10.5。 除去第二水相,然后通过蒸馏从第二有机相中除去一价醇。 再次将第二有机相的pH值设定为8.0〜10.5,通过分馏回收1,3-二醇。

    Process for preparing anhydrous cyclic imido esters
    7.
    发明授权
    Process for preparing anhydrous cyclic imido esters 失效
    制备无水环状酰亚胺酯的方法

    公开(公告)号:US4574157A

    公开(公告)日:1986-03-04

    申请号:US508621

    申请日:1983-06-28

    Inventor: Walter K. Homann

    CPC classification number: C07D265/08 C07D263/12

    Abstract: For the preparation of pure, anhydrous cyclic imido esters, nitriles are reacted with amino alcohols with splitting off of ammonia at temperatures of 90.degree.-230.degree. C. under a pressure of 1.1-10 bar. The catalysts employed are metallic compounds. The process results in substantially shorter reaction times.

    Abstract translation: 为了制备纯的无水环状亚氨基酯,腈在与氨基醇反应,在90〜-230℃的温度下,在1.1-10巴的压力下分解氨。 所使用的催化剂是金属化合物。 该过程导致显着更短的反应时间。

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