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Nitrate reduction to nitrogen in wastewater using mesoporous carbon encapsulated Pd-Cu nanoparticles combined with in-situ electrochemical hydrogen evolution.
Cai, Wenlue; Chen, Chen; Bao, Chenyu; Gu, Jia-Nan; Li, Kan; Jia, Jinping.
Afiliación
  • Cai W; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
  • Chen C; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
  • Bao C; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
  • Gu JN; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
  • Li K; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China. Electronic address: likan@sjtu.edu.cn.
  • Jia J; School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, PR China.
J Environ Manage ; 362: 121346, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38824884
ABSTRACT
The conversion of NO3--N to N2 is of great significance for zero discharge of industrial wastewater. Pd-Cu hydrogenation catalysis has high application prospects for the reduction of NO3--N to N2, but the existing form of Pd-Cu, the Pd-Cu mass ratio and the H2 evolution rate can affect the coverage of active hydrogen (*H) on the surface of Pd, thereby affecting N2 selectivity. In this work, mesoporous carbon (MC) is used as support to disperse Pd-Cu catalyst and is applied in an in-situ electrocatalytic H2 evolution system for NO3--N removal. The Pd-Cu particles with the average size of 6 nm are uniformly encapsulated in the mesopores of MC. Electrochemical in-situ H2 evolution can not only reduce the amount of H2 used, but the H2 bubbles can also be efficiently dispersed when PPy coated nickel foam (PPy/NF) is used as cathode. Moreover, the mesoporous structure of MC can further split H2 bubbles, reducing the coverage of *H on Pd. The highest 77% N2 selectivity and a relatively faster NO3--N removal rate constant (0.10362 min-1) can be achieved under the optimal conditions, which is superior to most reported Pd-Cu catalytic systems. The prepared catalyst is further applied to the denitrification of actual deplating wastewater. NO3--N with the initial concentration of 650 mg L-1 can be completely removed after 180 min of treatment, and the TN removal can be maintained at 72%.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carbono / Aguas Residuales / Hidrógeno / Nitratos / Nitrógeno Idioma: En Revista: J Environ Manage Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carbono / Aguas Residuales / Hidrógeno / Nitratos / Nitrógeno Idioma: En Revista: J Environ Manage Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido