Pyrolysis regulation of ZIF-8 to construct a robust multifunctional N-doped macroporous carbon for lipase immobilization

热解 碳纤维 脂肪酶 化学工程 材料科学 生物柴油 X射线光电子能谱 金属有机骨架 背景(考古学) 化学 热稳定性 兴奋剂 催化作用 有机化学 复合材料 吸附 古生物学 复合数 工程类 生物 光电子学
作者
Hao Zhou,Yongheng Shi,Lingmei Dai,Dehua Liu,Wei Du
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:473: 145218-145218 被引量:15
标识
DOI:10.1016/j.cej.2023.145218
摘要

Pyrolyzing ZIF-8 into N-doped carbon is now inspiring new potential of ZIF-8 for extensive applications. However, the exploration of such ZIF-8-derived carbon for biotechnological applications has been rarely investigated, especially in this context that imidazole derivatives are of rich functionality in life science. Herein, we reported a facile temperature-dependent pyrolysis method to achieve the effective N-doping in ZIF-8-derived macroporous carbon, which was systematically investigated for the immobilization of lipase from Thermomyces lanuginosus (TLL) in biodiesel production. MNC-600 (macroporous N-doped carbon derived at 600 °C) exhibited the best immobilization performance, with the highest specific activity of 190.6 U mg−1, a 36.9% increase than free TLL. Moreover, MNC-600@TLL showed superior effectiveness and robustness in biodiesel production. A much faster rate of conversion and the highest biodiesel yield of 87.4% were observed. After eight successive batches of recycling, MNC-600@TLL retained 93.4% of its initial activity. XPS analysis revealed the evolution of N species during the pyrolysis of ZIF-8. It was proposed that the abundant doping of pyrrolic N species played a major role in the surprising performance of MNC-600, mainly through hydrogen bonding interactions, which simultaneously realized the activation of reactants as well as the in-situ hydrophobization of biocatalyst. This report is anticipated to pave a way for the exploration of ZIF-8-derived N-doped carbon for extensive biotechnological applications.
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