格式化
吸附
甲酸脱氢酶
水溶液
化学工程
动力学
材料科学
化学
表面改性
催化作用
有机化学
物理化学
量子力学
物理
工程类
作者
Shadeera Rouf,Yaser E. Greish,Bart Van der Bruggen,Sulaiman Al‐Zuhair
标识
DOI:10.1016/j.crcon.2023.09.003
摘要
Post synthetic modification of a hydrophilic metal–organic framework (MOF), HKUST-1, with stearic acid (SA) was carried out to enhance the stability of HKUST-1 in aqueous solution to be used as a support for formate dehydrogenase (FDH) used for CO2 conversion to formate. SA modification improved the hydrophobicity without affecting the morphology and crystal structure of MOF. Adsorption of FDH on the modified MOF (SA@HKUST-1) was compared to that of the native HKUST-1 and ZIF-L. The adsorption kinetics on all MOFs was found to follow pseudo-second order kinetics and the isotherm was best described by Freundlich model. The high stability of SA@HKUST-1 and enhanced hydrophobic interaction between support and CO2 resulted in high catalytic efficiency and stability of FDH@SA@HKUST-1. The immobilized enzyme retained 95.1% of its initial activity after 4 cycles of repeated use. It was also shown that FDH@SA@HKUST-1 retained morphology and crystal structure after repeated use. Results of the present work provide novel insight into the influence of hydrophobic MOFs on the activity and stability of immobilized FDH. These findings are expected to assist in developing highly active and stable biocatalysts for CO2 hydrogenation at commercial level.
科研通智能强力驱动
Strongly Powered by AbleSci AI