Accelerating Catalytic Oxyanion Reduction with Inert Metal Hydroxides

Authors

Jinyu Gao
Qiang Zhao
Cheng Tan
Shaohua Xie
Yadong Yin
Fudong Liu
Haizhou Liu
Baoliang Chen
Jinyong Liu

Publication Date

1-12-2023

Journal

Environmental Science & Technology

Abstract

Adding CrIII or AlIII salts into the water suspension of platinum group metal (PGM) catalysts accelerated oxyanion pollutant reduction by up to 600%. Our initial attempts of adding K2CrVIO4, K2CrVI2O7, or KCrIII(SO4)2 into Pd/C enhanced BrO3– reduction with 1 atm H2 by 6-fold. Instrument characterizations and kinetic explorations collectively confirmed the immobilization of reduced CrVI as CrIII(OH)3 on the catalyst surface. This process altered the ζ-potentials from negative to positive, thus substantially enhancing the Langmuir–Hinshelwood adsorption equilibrium constant for BrO3– onto Pd/C by 37-fold. Adding AlIII(OH)3 from alum at pH 7 achieved similar enhancements. The Cr–Pd/C and Al–Pd/C showed top-tier efficiency of catalytic performance (normalized with Pd dosage) among all the reported Pd catalysts on conventional and nanostructured support materials. The strategy of adding inert metal hydroxides works for diverse PGMs (palladium and rhodium), substrates (BrO3– and ClO3–), and support materials (carbon, alumina, and silica). This work shows a simple, inexpensive, and effective example of enhancing catalyst activity and saving PGMs for environmental applications.

Keywords

aluminum, chromium, chlorate, bromate, catalyst support, zeta-potential, X-ray photoelectron spectroscopy (XPS), scanning transmission electron microscopy (STEM)

Comments

Supplementary Materials

PMID: 36633933