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Surface modification of HKUST-1 for enhanced activity of immobilized formate dehydrogenase used in CO_(2)hydrogenation

作     者:Shadeera Rouf Yaser E.Greish Bart Van der Bruggen Sulaiman Al-Zuhair 

作者机构:Department of Chemical and Petroleum EngineeringUAE University15551 Al AinUnited Arab Emirates Department of ChemistryUAE University15551 Al AinUnited Arab Emirates Department of Chemical EngineeringKU Leuven3000 LeuvenBelgium 

出 版 物:《Carbon Resources Conversion》 (碳资源转化(英文))

年 卷 期:2024年第7卷第1期

页      面:89-102,F0004页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 070304[理学-物理化学(含∶化学物理)] 08[工学] 0817[工学-化学工程与技术] 0703[理学-化学] 

基  金:The authors express their gratitude to Zayed Center of Health Sciences(grant number 31R236) the College of Graduate Studies(PhD fund 31N438)at UAE University,for financially supporting this study 

主  题:CO_(2)hydrogenation Formate dehydrogenase Metal organic frameworks Hydrophobic MOFs Formate 

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 CO_(2)conversion to *** modification improved the hydrophobicity without affecting the morphology and crystal structure of *** of FDH on the modified MOF(SA@HKUST-1)was compared to that of the native HKUST-1 and *** adsorption kinetics on all MOFs was found to follow pseudo-second order kinetics and the isotherm was best described by Freundlich *** high stability of SA@HKUST-1 and enhanced hydrophobic interaction between support and CO_(2)resulted in high catalytic efficiency and stability of FDH@SA@*** immobilized enzyme retained 95.1%of its initial activity after 4 cycles of repeated *** was also shown that FDH@SA@HKUST-1 retained morphology and crystal structure after repeated *** of the present work provide novel insight into the influence of hydrophobic MOFs on the activity and stability of immobilized *** findings are expected to assist in developing highly active and stable biocatalysts for CO_(2)hydrogenation at commercial level.

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