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Effects of Reaction Operation Policies on Properties of Core–Shell Polymer Supports Used for Preparation of Highly Active Biocatalysts

机译:反应运作政策对高活性生物催化剂的核心 - 壳聚合物支撑件性能的影响

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摘要

Core-shell polymer supports with different morphological features and compositions are prepared through combined suspension and emulsion polymerizations. It is shown that proper manipulation of the divinylbenzene (DVB) feed content allows for maximization of specific areas, porosities, and mechanical resistances. Additionally, it is shown that feeding of previously prepared miniemulsions leads to core-shell particles with smaller specific areas, due to less efficient coating of the cores. Particularly, the combined manipulation of polymerization times and DVB feed compositions allows for production of particles with pronounced specific area (50 m(2) g(-1)) and porosity (0.30 cm(3) g(-1)). Produced core-shell polymer particles are employed as supports for the immobilization of lipase B from Candida antarctica, and the obtained enzymatic activities for both hydrolysis (A(hyd)) and esterification (A(est)) reactions are very high (A(hyd) = 34.7 +/- 3.8 U/g; A(est) = 3564.6 +/- 581 U/g), even when compared to activities obtained using the reference commercial biocatalyst Novozym 435 (A(hyd) = 7.6 +/- 1.8 U/g, A(est) = 2384.7 +/- 307.2 U/g). Finally, biocatalysts prepared with the core-shell supports present higher enzymatic activities than biocatalysts prepared with supports of higher specific area obtained through conventional emulsion polymerizations, indicating that the porous structure of the shell can be beneficial for the immobilization and activity of the enzymes.
机译:通过组合悬浮液和乳液聚合制备具有不同形态学特征和组合物的核 - 壳聚合物支持。结果表明,二乙烯基苯(DVB)饲料含量的适当操纵允许最大化特定区域,孔隙率和机械电阻。另外,由于芯的有效涂层,因此显示出先前制备的小乳液的进料导致具有较小特异性区域的核壳颗粒。特别地,聚合时间和DVB进​​料组合物的组合操纵允许用明显的特异性面积(50μm(2 )g(-1))和孔隙率(0.30cm(3 )g(-1))产生颗粒。制备的核 - 壳聚合物颗粒作为从念珠菌抗蚁癌固定的脂肪酶B的载体,以及用于水解的酶活性(A(HYD))和酯化(A(EST))反应非常高(A(HYD) )= 34.7 +/- 3.8 U / g; a(EST)= 3564.6 +/- 581 U / g),即使与使用参考商业生物催化剂Novozym 435获得的活性相比(a(hyd)= 7.6 +/- 1.8 U / G,A(EST)= 2384.7 +/- 307.2 U / g)。最后,用核壳支撑件制备的生物催化剂具有比通过通过常规乳液聚合所获得的较高特异性面积所述制备的生物催化剂的酶活性更高,表明壳的多孔结构可以有利于酶的固定和活性。

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