Xiangxiang Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Xiangxiang Wang has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Bai Sun
Engineering Research Center of Building Energy Efficiency Control and Evaluation, Ministry of Education, Anhui Jianzhu University, Hefei 230601, China
1 shared publication - Fengshou Zhao
Engineering Research Center of Building Energy Efficiency Control and Evaluation, Ministry of Education, College of Environment and Energy Engineering, Anhui Jianzhu University, Hefei 230601, China
1 shared publication - Hao Huang
Engineering Research Center of Building Energy Efficiency Control and Evaluation, Ministry of Education, College of Environment and Energy Engineering, Anhui Jianzhu University, Hefei 230601, China
1 shared publication - Mingjian Yi
Anhui Institute of Urban and Rural Green Development and Urban Renewal, College of Environment and Energy Engineering, Anhui Jianzhu University, Hefei 230601, China
1 shared publication - Rui Liu
Engineering Research Center of Building Energy Efficiency Control and Evaluation, Ministry of Education, College of Environment and Energy Engineering, Anhui Jianzhu University, Hefei 230601, China
1 shared publication - Shengnan He
Institutes of Physical Science and Information Technology, Anhui University, Hefei 230039, P. R. China
1 shared publication
Latest Publications
- Open Access
Efficiently Degrading RhB Using Bimetallic Co3O4/ZnO Oxides: Ultra-Fast and Persistent Activation of Permonosulfate
To address the issues of poor Co2+ regeneration and limited interfacial electron transfer in heterogeneous catalytic systems, this study proposes the synthesis of highly efficient and stable Co3O4/ZnO composites through the pyrolysis–oxidation reaction of Co/Zn MOFs for the degradation of rhodamine B (RhB) using activated peroxymonosulfate (PMS). The results confirmed that the catalyst exhibited a high electron transfer capacity, and the synergistic effect between the bimetals enhanced the reversible redox cycle of Co3+/Co2+. Under optimal conditions, complete removal of RhB was achieved in just 6 min using the Co3O4/ZnO composite, which demonstrated excellent stability after five cycles. Furthermore, the catalyst exhibited a high degradation efficiency in real water samples with a total organic carbon (TOC) removal rate of approximately 65% after 60 min. The electrochemical measurements, identification of active species, and X-ray photoelectron spectroscopy (XPS) analysis revealed that non-radicals (1O2 and direct charge transfer) played a major role in the degradation of RhB. Finally, the potential mechanisms and degradation pathways for RhB degradation using this catalyst were systematically investigated. This study opens new avenues for the development of efficient and stable PMS catalysts, and provides insights into the preparation of other emerging metal oxides.
Open AccessEfficiently Degrading RhB Using Bimetallic Co3O4/ZnO Oxides: Ultra-Fast and Persistent Activation of Permonosulfate
To address the issues of poor Co2+ regeneration and limited interfacial electron transfer in heterogeneous catalytic systems, this study proposes the synthesis of highly efficient and stable Co3O4/ZnO composites through the pyrolysis–oxidation reaction of Co/Zn MOFs for the degradation of rhodamine B (RhB) using activated peroxymonosulfate (PMS). The results confirmed that the catalyst exhibited a high electron transfer capacity, and the synergistic effect between the bimetals enhanced the reversible redox cycle of Co3+/Co2+. Under optimal conditions, complete removal of RhB was achieved in just 6 min using the Co3O4/ZnO composite, which demonstrated excellent stability after five cycles. Furthermore, the catalyst exhibited a high degradation efficiency in real water samples with a total organic carbon (TOC) removal rate of approximately 65% after 60 min. The electrochemical measurements, identification of active species, and X-ray photoelectron spectroscopy (XPS) analysis revealed that non-radicals (1O2 and direct charge transfer) played a major role in the degradation of RhB. Finally, the potential mechanisms and degradation pathways for RhB degradation using this catalyst were systematically investigated. This study opens new avenues for the development of efficient and stable PMS catalysts, and provides insights into the preparation of other emerging metal oxides.