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