可重用性
金属有机骨架
吸附
固定化酶
脂肪酶
化学工程
催化作用
多孔性
化学
材料科学
色谱法
有机化学
酶
工程类
计算机科学
程序设计语言
软件
作者
Reem Shomal,Mohammad Ali Abdelkareem,A.G. Olabi,Sulaiman Al‐Zuhair
标识
DOI:10.1016/j.mtsust.2023.100632
摘要
In recent years, metal–organic frameworks (MOFs) have emerged as promising supports for enzyme immobilization because they are highly designable and structurally diverse. However, the high porosities of conventional MOFs cannot be fully utilized for reactions involving large molecules, such as triglyceride transesterification reactions that produce biodiesel. Macroporous MOFs have been used to enhance diffusivity and, consequently, the reaction rate. Modifying MOFs with alginate to form MOF–polymer beads has also been proposed as a method for simplifying separation and reusability. Macroporous ZIF-8 (M-ZIF-8), sodium alginate ZIF-8 beads (SA@ZIF-8), and M-ZIF-8 combined with SA@ZIF-8 (SA@M-ZIF-8) were prepared for immobilizing lipase. M-ZIF-8 showed the highest adsorption capacity of 113.7 mg/g at 40 °C and was found to be more thermodynamically stable than ZIF-8. The experimental data for all three supports are best fitted to the Freundlich isotherm model. The adsorption kinetic data for M-ZIF-8 and SA@M-ZIF-8 are best described by a pseudo-first-order model, whereas a pseudo-second-order model provided a better fit for SA@M-ZIF-8. Lipase immobilized on M-ZIF-8 showed the highest catalytic activity, whereas that immobilized on SA@M-ZIF-8 showed the best reusability.
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