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Yongbing Xie

Researcher at Chinese Academy of Sciences

Publications -  111
Citations -  5009

Yongbing Xie is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 34, co-authored 98 publications receiving 3213 citations. Previous affiliations of Yongbing Xie include Tianjin University.

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Organic pollutants removal in wastewater by heterogeneous photocatalytic ozonation

TL;DR: The present overview dissects the heterogeneous catalysts and the influences of different operational parameters, followed by the discussion on the kinetics, mechanism, economic feasibility and future trends of this integrated technology.
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Efficient Catalytic Ozonation over Reduced Graphene Oxide for p-Hydroxylbenzoic Acid (PHBA) Destruction: Active Site and Mechanism

TL;DR: Reduced graphene oxide with a low level of structural defects was synthesized via a scalable method for catalytic ozonation of p-hydroxylbenzoic acid (PHBA) and metal-free rGO materials were found to exhibit a superior activity in activating ozone for catalysttic oxidation of organic phenolics.
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Reactive Oxygen Species and Catalytic Active Sites in Heterogeneous Catalytic Ozonation for Water Purification

TL;DR: The catalytic active sites and adsorption behaviors of O3 molecules on the catalyst surface are regarded as the key clues for further elucidating the O3 activation processes, evolution of reactive oxygen species (ROS), organic oxidation pathways.
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2D/2D nano-hybrids of γ-MnO2 on reduced graphene oxide for catalytic ozonation and coupling peroxymonosulfate activation

TL;DR: Two-dimensional reduced graphene oxide was employed as both a shape-directing medium and support to fabricate 2D γ-MnO2/2D rGO nano-hybrids via a facile hydrothermal route for catalytic ozonation of 4-nitrophenol.
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Single-Atom Mn-N4 Site-Catalyzed Peroxone Reaction for the Efficient Production of Hydroxyl Radicals in an Acidic Solution.

TL;DR: A heterogeneous catalyst comprised of single Mn atoms anchored on graphitic carbon nitride is described, which effectively overcome such the drawback by altering the reaction pathway and, thus, dramatically promotes •OH generation in acid solution.