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Method of separation of glutamic acid of the residual liquid sugar juices after separation of the sugar

机译:分离糖后残留液体糖汁中谷氨酸的分离方法

摘要

Glutamic acid is prepared by concentrating the pyrrolidone carboxylic acid-containing residual liquids which are obtained after the production of sugar from sugar-containing juices and from which the remaining sugar or a large proportion thereof has been removed, heating the concentrate with an alkaline earth metal oxide or hydroxide for approximately 10 to 15 minutes at a temperature of 80 DEG to 110 DEG C., cooling, diluting with one or more organic polar liquids or aqueous organic polar liquids, separating solids from the resulting liquid, removing the organic liquid by evaporation, concentrating the remaining liquid to a specific gravity of 1.2 to 1.4, hydrolysing this solution of pyrrolidone carboxylic acid with acid or alkali, and concentrating and adjusting the hydrolysate to approximately the isoelectric point of glutamic acid in order to precipitate said acid. Suitable starting materials are desugarized molasses, Steffen process waste waters and vinasse. Preferably 1 to 3 parts by weight of organic polar liquid are added to 1 part by weight of alkaline earth metal oxide or hydroxide-evaporated starting solution mixture. The evaporated starting solution preferably contains 2-15 per cent by weight of the alkaline earth metal oxide or hydroxide. Calcium oxide and hydroxide are specified for the latter purpose. Methanol and ethanol are specified as suitable organic polar liquids. The hydrolysis step is preferably effected with hydrochloric acid, as much as possible of the NaCl formed being removed.
机译:通过浓缩含吡咯烷酮羧酸的残留液体来制备谷氨酸,所述残留液体是从含糖果汁中制糖后获得的,并且从中除去了剩余的糖或其大部分,并用碱土金属加热浓缩物。在80℃至110℃的温度下,用氧化物或氢氧化物处理约10至15分钟,冷却,用一种或多种有机极性液体或含水有机极性液体稀释,从所得液体中分离出固体,通过蒸发除去有机液体将剩余的液体浓缩至比重为1.2至1.4,将该吡咯烷酮羧酸溶液用酸或碱水解,并且将水解产物浓缩并调节至近似谷氨酸的等电点以沉淀所述酸。合适的原料是脱糖糖蜜,Steffen工艺废水和酒糟。优选将1至3重量份的有机极性液体添加至1重量份的碱土金属氧化物或氢氧化物蒸发的起始溶液混合物中。蒸发的起始溶液优选包含2-15重量%的碱土金属氧化物或氢氧化物。氧化钙和氢氧化钙被指定用于后一目的。甲醇和乙醇被指定为合适的有机极性液体。水解步骤优选用盐酸进行,尽可能多地除去形成的NaCl。

著录项

  • 公开/公告号FR1156050A

    专利类型

  • 公开/公告日1958-05-12

    原文格式PDF

  • 申请/专利号FRD1156050

  • 发明设计人

    申请日1956-08-20

  • 分类号A23J1;A23J3/32;

  • 国家 FR

  • 入库时间 2022-08-23 20:28:50

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