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A Miniature Membrane Reactor for Evaluation of Process Design Options on the Enzymatic Degradation of Pectin

机译:微型膜反应器评价酶法降解果胶的工艺设计方案

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摘要

The objective of this paper is to assess if a membrane microbioreactor system could potentially be used to diagnose consequences of different process design and reactor operation options relevant for larger-scale enzymatic degradation of pectin reactions. The membrane microbioreactor prototype was fabricated from poly(methylmethacrylate) (PMMA) and poly(dimethylsiloxane) (PDMS) with a working volume of ∼190 μL. The prototype also contained the necessary sensors and actuators, i.e., pressure transducer, mixing via magnetic stirrer bar and a temperature controller. The functionality of the prototype was demonstrated by performing a continuous enzymatic degradation of pectin experiment for a range of reactor conditions: different membrane molecular weight cutoff (MWCO) values, enzyme-to-substrate ratios (E/S), and substrate feeding rates (F) were assessed. Based on the experimental data, it was found that the apparent reaction rate increased from 0.11 μmol/h to 0.13 μmol/h when the E/S ratio was doubled from 0.2% (g/g) to 0.4% (g/g). In contrast, when the substrate feeding rate was reduced from 200 μL/h to 100 μL/h (i.e., longer residence time), a higher yield was achieved (producing a pectin fragment concentration of 0.82 mM in the permeate) and the apparent reaction rate increased by ∼50% (i.e., from 0.11 μmol/h to 0.17 μmol/h). Clearly, this signifies that the substrate feeding rate is a critical variable that influences the conversion rate and the process yield. The data also showed that the process design affected the membrane rejection profile. The results obtained thus underlined the suitability of a miniature membrane reactor system for evaluating different process design options that are relevant for larger-scale reactions of enzymatic pectin degradation.
机译:本文的目的是评估膜微生物反应器系统是否可以潜在地用于诊断与果胶反应的大规模酶促降解相关的不同工艺设计和反应器操作选项的后果。膜微生物反应器原型是由工作量约为190μL的聚甲基丙烯酸甲酯(PMMA)和聚二甲基硅氧烷(PDMS)制成的。原型还包含必要的传感器和执行器,即压力传感器,通过磁力搅拌棒和温度控制器进行混合。通过对一系列反应器条件进行果胶实验的连续酶促降解来证明原型的功能:不同的膜分子量截断值(MWCO)值,酶与底物之比(E / S)和底物进料速率( F)进行了评估。根据实验数据,发现当E / S比从0.2%(g / g)翻倍至0.4%(g / g)时,表观反应速率从0.11μmol/ h增加至0.13μmol/ h。相反,当底物进料速率从200μL/ h降低至100μL/ h(即,更长的停留时间)时,可获得更高的产量(在渗透液中产生的果胶碎片浓度为0.82 mM)和表观反应速率增加了约50%(即从0.11μmol/ h增加到0.17μmol/ h)。显然,这表明基材的进料速度是影响转化率和工艺产量的关键变量。数据还表明,工艺设计影响了膜的截留率。因此获得的结果强调了微型膜反应器系统用于评估与酶果胶降解的大规模反应有关的不同工艺设计方案的适用性。

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