4.7 Article

Perchlorate catalysis reduction by benzalkonium chloride immobilized biomass carbon supported Re-Pd bimetallic cluster particle electrode

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 348, Issue -, Pages 765-774

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2018.05.052

Keywords

Re-Pd/BC particles electrode; Three-dimensional electrochemical reactor; Electro-reduction; Perchlorate catalysis reduction

Funding

  1. National Natural Science Foundation of China [51679083]
  2. Interdisciplinary Research Funds for Hunan University [2015JCA03]
  3. scientific and technological project of Changsha City [KQ1602029]
  4. PetroChina Innovation Foundation [2016D-5007-0703]
  5. project of Shenzhen Science and Technology Funds [JCYJ20160530193913646]

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This work had demonstrated a novel and high-efficiency perchlorate reduction particle electrode using benzalkonium chloride as dynamics strengthener and coupling with rhenium (Re) and palladium (Pd) nanoparticles (Re-Pd/BC). Perchlorate ions could be rapidly adsorbed in the presence of benzalkonium chloride, facilitating its subsequent reduction on the Re-Pd/BC particle electrode. On the basis of the characterization results and kinetics analysis, a synergistic effect of Re and Pd was observed, perchlorate could be efficiently reduced and completely converted into chlorine in optimized conditions (pH 3.0, anaerobic and current density 20 mA/cm(2)) and the reduction rate constant of Re-Pd/BC was 0.9451 L-1 g(cat)(-1). The superfluous oxygen in solution could lead to Re-Pd/BC deactivation, and increased current density was beneficial of electro-reduction. The increased pH lead to decrease of reduction efficiency, and the coexisting anion of nitrate could be competed with perchlorate for reduction sites which lead to decrease of reduction rate. Based on the experimental results, it was found that the existing form of Re and Pd on the surface of Re-Pd/BC, the number of atomic H* and current density played an important role in perchlorate electro-reduction process.

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