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用于高效电催化降解甲酚的硼掺杂金刚石薄膜电极的制备。

Fabrication of boron-doped diamond films electrode for efficient electrocatalytic degradation of cresols.

机构信息

Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, PR China; University of Chinese Academy of Sciences, Beijing, 100049, PR China.

Beijing Key Laboratory of Fuels Cleaning and Advanced Catalytic Emission Reduction Technology, College of Chemical Engineering, Beijing Institute of Petrochemical Technology, Beijing, 102617, PR China.

出版信息

Chemosphere. 2020 May;246:125786. doi: 10.1016/j.chemosphere.2019.125786. Epub 2019 Dec 31.

Abstract

The choice of anode materials has a significant influence on the electrocatalytic degradation of organics. Accordingly, the electrocatalytic activity of several active anodes (Ti/Ru-Ir, Ti/Ir-Ta, Ti/Pt) and non-active anodes (Ti/PbO, Ti/SnO, Si/BDD (boron-doped diamond)) was compared by electrocatalytic degradation of m-cresol. The results indicated Si/BDD electrode had the strongest mineralization ability and the lowest energy consumption. And the order of the activity of m-cresol degradation was as follows: Si/BDD > Ti/SnO>Ti/PbO>Ti/Pt > Ti/Ir-Ta > Ti/Ru-Ir. Also their intermediate products were compared. The effects of experimental parameters on electrocatalytic degradation of m-cresol with Si/BDD electrode showed m-cresol conversion was affected slightly by the electrode spacing and electrolyte concentration, but affected greatly by the temperature and current density. And smaller electrode spacing and current density, higher electrolyte concentration and temperature were beneficial to reduce energy consumption. Their degradation processes were all accord with the pseudo-first-order reaction kinetics completely. In addition, the results of electrocatalytic degradation of m, o, p-cresol indicated there was almost no significant difference on conversion rate between cresols isomers with the current density of 30 mA cm. However, the influence of group position was shown when the current density was reduced to 10 mA cm and cresols conversion followed the sequence of m-cresol ≈ o-cresol > p-cresol.

摘要

阳极材料的选择对有机物的电催化降解有重要影响。因此,通过间甲酚的电催化降解比较了几种活性阳极(Ti/Ru-Ir、Ti/Ir-Ta、Ti/Pt)和非活性阳极(Ti/PbO、Ti/SnO、Si/BDD(掺硼金刚石))的电催化活性。结果表明,Si/BDD 电极具有最强的矿化能力和最低的能耗。间甲酚降解活性顺序为:Si/BDD>Ti/SnO>Ti/PbO>Ti/Pt>Ti/Ir-Ta>Ti/Ru-Ir。并比较了它们的中间产物。实验参数对 Si/BDD 电极电催化降解间甲酚的影响表明,电极间距和电解液浓度对间甲酚转化率的影响较小,但温度和电流密度的影响较大。较小的电极间距和电流密度、较高的电解液浓度和温度有利于降低能耗。它们的降解过程均完全符合准一级反应动力学。此外,间甲酚、邻甲酚和对甲酚电催化降解的结果表明,在电流密度为 30 mA cm 时,间甲酚异构体的转化率几乎没有显著差异。然而,当电流密度降低到 10 mA cm 时,基团位置的影响就显现出来,间甲酚的转化率顺序为间甲酚≈邻甲酚>对甲酚。

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