Liquid phase catalytic hydrogenation reduction of Cr(VI) using highly stable and active Pd/CNT catalysts coated by
Minghui Li1, Jiao He1, Yuqiong Tang1
1State Key Laboratory of Pollution Control and Resource Reuse, Jiangsu Key Laboratory of Vehicle Emissions Control, School of the Environment, Nanjing University, Nanjing 210093, PR China.
Abstract:
Liquid catalytic hydrogenation is a green and cost-effective technique for the reductive removal of pollutants in water. Supported noble metals are the most frequently used catalysts in liquid phase catalytic hydrogenation, whereas marked catalyst deactivation is commonly identified. In this study, we coated supported Pd catalyst on carbon nanotube (denoted as Pd/CNT) by different overcoatings (including SiO2, carbon and N-doped carbon) to prevent catalyst deactivation. The activities of the coated catalysts for liquid phase catalytic hydrogenation reduction of hexavalent chromium (Cr(VI)) differed with the overcoating properties. Negligible Cr(VI) conversion was observed on SiO2 coated Pd/CNT, while feasible Cr(VI) reduction was identified on carbon coated (denoted as Pd/CNT@C) and N-doped carbon coated catalysts (denoted as Pd/CNT@CN). Pd/CNT@CN exhibited a much higher catalytic activity than Pd/CNT@C, which was ascribed to the stronger Cr(VI) adsorption on CN overcoating. The catalytic activity of Pd/CNT@CN was positively correlated with the conductivity and hydrophilicity of CN overcoating, which could be optimized by varying carbonization temperature. Furthermore, Pd/CNT@CN retained its initial activity after ten consecutive catalyst cycles without any deactivation, whereas Pd/CNT only retained 8.2% of its initial activity, reflecting much higher catalytic stability of Pd/CNT@CN than Pd/CNT. The findings in the present study highlight that liquid catalytic reduction using Pd/CNT@CN as the catalyst is a highly stable and effective method to remove Cr(VI) in water.
More Related Videos
19:58Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
09:17Reductive Electropolymerization of a Vinyl-containing Poly-pyridyl Complex on Glassy Carbon and Fluorine-doped Tin Oxide Electrodes
Published on: January 30, 2015
Related Concept Videos
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Phase I Reactions: Reductive Reactions
Oxidation-Reduction Reactions
