4.8 Article

Combination of Pd-Cu Catalysis and Electrolytic H2 Evolution for Selective Nitrate Reduction Using Protonated Polypyrrole as a Cathode

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 53, 期 23, 页码 13868-13877

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.9b04447

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资金

  1. National Natural Science Foundation of China [21976119, 21607103, 21737002]
  2. Centre of Hydrogen Science, Shanghai Jiao Tong University, China

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Pd-Cu catalysis is combined with in situ electrolytic H-2 evolution for NO3- reduction with protonated polypyrrole (PPy) as a cathode. The surface of PPy is not only beneficial for H-2 evolution, but exclusive for NO(3)(- )adsorption, and thus inhibits NO3- reduction. Meanwhile, the in situ H-2 generation exhibits a much higher utilization efficiency because of the smaller bubble size and higher dispersion. The Pd-Cu catalysts with the ratios of 6:1 and 4:1 exhibit the highest NO3- N removal (100%) and N-2 selectivity (93-95%) after 90 min. In comparison with the results obtained with other cathode materials (Ti, Cu, Co3O4, and Fe2O3) and obtained by other researchers, the new process shows a faster NO3--N reduction rate and much higher N-2 selectivity. However, the O-2 generated on the anode can oxidize Cu to Cu2O that may work as the catalyst for NO3- -N reduction to NH4+-N by H-2 , resulting in more than 60% NH4+-N generated without a proton exchange membrane. Both the PPy film and Pd-Cu catalyst exhibit good stability and there is no Cu2+ or Pd2+ in solution after reaction. Real industrial wastewater is further treated in this system, the NO3--N is reduced from 670 mg L(-1 )to less than 100 mg L-1 in 90 min, and only little amount of NH4+-N is generated.

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