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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:反应操作策略对用于制备高活性生物催化剂的核壳聚合物载体性能的影响

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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:具有不同形态特征和组成的核-壳聚合物载体是通过悬浮和乳液聚合相结合制备的。结果表明,适当控制二乙烯基苯(DVB)的进料量可以使比表面积,孔隙率和机械抗性最大化。此外,显示出,由于核的包覆效率较低,先前制备的细乳液的进料导致具有较小比表面积的核-壳颗粒。特别是,聚合时间和DVB进​​料组成的组合操作可生产具有明显比表面积(50 m(2)g(-1))和孔隙率(0.30 cm(3)g(-1))的颗粒。产生的核-壳聚合物颗粒用作固定化南极假丝酵母脂肪酶B的载体,获得的水解(A(hyd))和酯化(A(est))反应的酶活性都很高(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 +/- 307.2U / g)。最后,用核-壳载体制备的生物催化剂比通过常规乳液聚合获得的用比表面积更高的载体制备的生物催化剂具有更高的酶促活性,这表明壳的多孔结构可有利于酶的固定和活性。

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