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polymeric membranes for reverse osmosis high flow of water and high salt rejection and method of preparing such membranes

机译:用于反渗透,高水流量和高除盐率的聚合物膜及其制备方法

摘要

1391559 Reverse osmosis membranes MONTECATINI EDISON SpA 1 Jan 1973 [30 Dec 1971] 59662/72 Heading B5B An isotropic reverse osmosis membrane of a polypiperazinamide having recurring units of the general formula is disclosed, where R is an organic substituent of the piperazine ring, x is from 1 to 8 and Y is an oxygen or sulphur atom. Preferably R is C 1 to C 4 alkyl, especially methyl or ethyl and x = 1 or 2. Specified polypiperazinamides include poly (2-methyl piperazin-thiofurazanamide), poly (2 - methylpiperazin - furazanamide), poly (trans - 2,5 - dimethylpiperazin - thio furazanamide), and poly (trans - 2,5 - dimethyl piperazin-furazanamide). A solution of the polypiperazinamide in an organic water soluble aprotic polar solvent is spread preferably at room temperature, on a smooth surface to form a film suitably of 0À002 to 0À2 cm. thickness, a membrane made therefrom by surface evaporation of the solvent, e.g. at 70‹ to 200‹ C., especially 80‹ to 180‹ C., for from 1 min. to 3 hours, especially 3 to 30 mins. and the membrane congulated by immersion in a coagulating bath, suitably water or an aqueous saline solution, e.g. of sodium or calcium chloride or magnesium sulphate, or alternatively mixtures of water with methanol, ethanol or isopropyl alcohol. The congulating liquid temperature is suitably 0‹ to 30‹ C. especially 0‹ to 5‹C. Specified solvents include dimethylformamide, dimethyl-acetamide, dimethyl sulphoxide, N- methylpyrrolidone and tetramethyl sulphone, which may also contain dissolved therein, water, and a salt soluble in water and in the organic solvent, e.g. lithium chloride, bromide and nitrate, calcium, zinc and magnesium chlorides and magnesium chlorate. The membrane may be subjected to a heat treatment before use by immersion in water at 60-100‹ C. for from 1 min. to 5 hours.
机译:1391559反渗透膜MONTECATINI EDISON SpA 1973年1月1日[1971年12月30日]标题B5B公开了具有通式重复单元的聚哌嗪酰胺的各向同性反渗透膜,其中R是哌嗪环的有机取代基,x是1至8,且Y是氧或硫原子。优选地,R是C 1至C 4烷基,尤其是甲基或乙基且x = 1或2。特定的聚哌嗪酰胺包括聚(2-甲基哌嗪-硫呋喃酰胺),聚(2-甲基哌嗪-呋喃酰胺),聚(反式-2,5 -二甲基哌嗪-硫呋喃酰胺)和聚(反式-2,5-二甲基哌嗪-呋喃酰胺)。聚哌嗪酰胺在有机水溶性非质子极性溶剂中的溶液最好在室温下铺展在光滑的表面上,以形成合适的0-002至0-2 cm的薄膜。厚度,通过溶剂例如溶剂的表面蒸发由其制成的膜。在70℃至200℃,尤其是80℃至180℃下放置1分钟。到3小时,尤其是3到30分钟。并通过浸入凝结浴中而使膜凝结,适当地用水或盐水溶液,例如水。氯化钠或氯化钙或硫酸镁,或水与甲醇,乙醇或异丙醇的混合物。凝结液体温度合适地为0℃至30℃,特别是0℃至5℃。特定的溶剂包括二甲基甲酰胺,二甲基乙酰胺,二甲基亚砜,N-甲基吡咯烷酮和四甲基砜,它们也可包含溶解于其中的水,水和可溶于水和有机溶剂的盐,例如有机溶剂。氯化锂,溴化物和硝酸盐,钙,锌和镁的氯化物以及氯酸镁。在使用之前,可通过在60-100°C的水中浸泡1分钟来对膜进行热处理。 5个小时。

著录项

  • 公开/公告号FR2166115B1

    专利类型

  • 公开/公告日1976-04-23

    原文格式PDF

  • 申请/专利权人 MONTECATINI EDISON SPA;

    申请/专利号FR19720046566

  • 发明设计人

    申请日1972-12-28

  • 分类号B01D13/00;C08G41/00;C08G53/00;

  • 国家 FR

  • 入库时间 2022-08-23 01:54:33

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