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Improving the Chemical Utilization Efficiency of Pd Hydrodechlorination Catalysts through Hydrogen-Spillover Empowered Synergy between Pd and TiNiN Support.

Authors :
Wang W
Zhang X
Ran W
Ma C
Sun J
Zhao M
Pan W
Liu J
Liu R
Jiang G
Source :
Environmental science & technology [Environ Sci Technol] 2024 Nov 20. Date of Electronic Publication: 2024 Nov 20.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

The sustainable and affordable environmental application of Pd catalysis needs further improvement of Pd mass activity. Besides the well-recognized importance of physical utilization efficiency─the ratio of surface atoms forming reactant-accessible reactive sites─a lesser-known fact is that the congestion of these reactive sites, which we term as the chemical utilization efficiency, also influences the mass activity. Herein, by leveraging the 100% physical utilization efficiency of a fully exposed Pd cluster (Pd <subscript> n </subscript> ) and the hydrogenation activity of TiNiN, we developed Pd <subscript> n </subscript> /TiNiN as a high physical and chemical utilization efficiency catalyst. During the catalytic hydrodechlorination of 4-chlorophenol and the subsequent hydrogenation of phenol, Pd <subscript> n </subscript> focuses on H <subscript>2</subscript> dissociation and C-Cl cleavage, while TiNiN facilitates the subsequent hydrogenation of phenol into less toxic cyclohexanone via H-spillover. This synergy results in a 20-40-fold increase in the hydrodechlorination rate. The enhanced chemical utilization efficiency of Pd informs the design of Pd <subscript> n </subscript> /TiNiN microspheres for the conversion of halogenated organics from pharmaceutical wastewater and the design of a fixed-bed reactor to transfer trace amounts of 4-CP from river water. Ultimately, this approach decentralizes the use of Pd in environmental catalysis and reduction processes.

Details

Language :
English
ISSN :
1520-5851
Database :
MEDLINE
Journal :
Environmental science & technology
Publication Type :
Academic Journal
Accession number :
39568214
Full Text :
https://doi.org/10.1021/acs.est.4c05860