Heteropoly Acid/Nitrogen Functionalized Onion‐like Carbon Hybrid Catalyst for Ester Hydrolysis Reactions. Issue 4 (25th November 2015)

• Record Type: Journal Article
• Authors: Liu, Wei; Qi, Wei; Guo, Xiaoling; Su, Dangsheng
• Is Part Of: Chemistry, an Asian journal. Volume 11:Issue 4(2016)
• Page Start: 491
• Page End: 497
• Publication Date: 2015-11-25
• Subjects: heterogeneous catalysis -- heteropoly acid -- hydrolysis -- onion-like carbon -- support; Chemistry -- Periodicals; 540.5
• DOI: 10.1002/asia.201500944
• Languages: English
• ISSNs: 1861-4728

Abstract

Abstract: A novel heteropoly acid (HPA)/nitrogen functionalized onion‐like carbon (NOLC) hybrid catalyst was synthesized through supramolecular (electrostatic and hydrogen bond) interactions between the two components. The chemical structure and acid strength of the HPA/NOLC hybrid have been fully characterized by thermogravimetric analysis, IR spectroscopy, X‐ray photoelectron spectroscopy, NH3 temperature‐programmed desorption and acid–base titration measurements. The proposed method for the fabrication of the HPA/NOLC hybrid catalyst is a universal strategy for different types of HPAs to meet various requirements of acidic or redox catalysis. The hydrophobic environment of NOLC effectively prevents the deactivation of HPA in an aqueous system, and the combination of uniformly dispersed HPA clusters and the synergistic effect between NOLC and HPA significantly promotes its activity in ester hydrolysis reactions, which is higher than that of bare PWA as homogeneous catalyst. The kinetics of the hydrolysis reactions indicate that the aggregation status of the catalyst particles has great influence on the apparent activity. Abstract : Know your onion‐like carbon : A heteropoly acid (HPA)/nitrogen functionalized onion‐like carbon (NOLC) hybrid catalyst was successfully synthesized. The hydrophobic environment of NOLC effectively prevents the deactivation of HPA in an aqueous system, and the synergistic effect between NOLC and HPA significantly promotes its activity in hydrolysis reactions.