乳酸发酵过程中乳酸胺的形成。1,4‐哌嗪‐(L,L)‐苯二甲酸酯的发酵生产及其作为苯二甲酸酯合成原料的应用(第二部分)

B. Kamm, M. Kamm, K. Richter, W. Reimann, A. Siebert
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引用次数: 13

摘要

介绍了一种利用可再生原料发酵生产1,4-哌嗪-(L,L)-dilactate的工艺及将该产品加工成L,L- dilactate的方法。对副干酪乳杆菌的乳酸发酵进行了改进,通过使用哌嗪水溶液代替氢氧化钠溶液来控制pH值。当pH为5.0时,可以生产化学计量组成的乳酸哌嗪。在发酵过程中,由5.0 kg葡萄糖和2.15 kg哌嗪生成6.65 kg 1,4-哌嗪-(L,L)-dilactate。通过超滤、纳滤和电渗析对发酵液进行分离、纯化和水溶液浓缩。所使用的膜的总产物保留率约为33%。采用真空蒸发法制备结晶盐。在专用玻璃反应器中将1,4-哌嗪-(L,L)-dilactate加工成L,L- dilactate。产品收率达70%。通过元素分析、溶解度、极性和光谱数据对纯化产物进行了表征。整个过程包括发酵阶段,纯化和浓缩的戊二酸哌嗪,以及后者的环化到戊二酸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation of aminium lactates in lactic acid fermentation. Fermentative production of 1,4‐piperazinium‐(L,L)‐dilactate and its use as a starting material for the synthesis of dilactide (Part 2)
A fermentation process for manufacturing 1,4-piperazinium-(L,L)-dilactate from renewable raw materials and a method for processing this product into L,L-dilactide are described. Lactic acid fermentation with Lactobacillus paracasei was modified in such a way that pH control occurred by using an aqueous solution of piperazine as a correcting agent instead of sodium hydroxide solution. The production of a stoichiometrically composed piperazinium lactate was possible when the pH was 5.0. From 5.0 kg of glucose and 2.15 kg of piperazine, 6.65 kg of 1,4-piperazinium-(L,L)-dilactate were formed in the fermentation process. Separation from fermentation broth, purification and concentration of the product in aqueous solutions were carried out by means of ultrafiltration, nanofiltration and electrodialysis. Total product retention by the membranes used was about 33%. The crystalline salt was obtained by vacuum evaporation. Processing of the 1,4- piperazinium-(L,L)-dilactate into L,L-dilactide was performed in a special glass reactor. A product yield of 70% was achieved. The purified product was characterized by elementary analysis, as well as solubility behaviour, polarity and spectroscopic data. An overall process consisting of the stages fermentation, purification and concentration of piperazinium dilactate as well as cyclization of the latter to dilactide is described.
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