Abstract

A novel electrode consisting of a Ti/PbO2 shell and Fe3O4/Sb–SnO2 particles was developed for electrochemical oxidation treatment of wastewater. Scanning electron microscope (SEM), X-ray diffraction (XRD), the current limiting method, toxicity experiments, and high-performance liquid chromatography were adopted to characterize its morphology, crystal structure, electrochemical properties, the toxicity of the wastewater, and hydroxyl radicals. Acid Red G (ARG), a typical azo dye, was additionally used to test the oxidation ability of the electrode. Results indicated that the 2.5D electrode could significantly improve the mass transfer coefficient and •OH content of the 2D electrode, thereby enhancing the decolorization, degradation, and mineralization effect of ARG, and reducing the toxicity of the wastewater. The experiments revealed that, at higher current density, lower dye concentration and higher temperature, the electrochemical oxidation of ARG favored. Under the condition of 50 mA/cm2, 25 °C, and 100 ppm, the ARG, Chemical Oxygen Demand (COD) and Total Organic Carbon (TOC) removal efficiency reached 100%, 65.89%, and 52.52%, respectively, and the energy consumption and the current efficiency were 1.06 kWh/g COD, 8.29%, and energy consumption for TOC and mineralization current efficiency were 3.81 kWh/g COD, 9.01%. Besides, the Fe3O4/Sb–SnO2 particles after electrolysis for 50 h still had remarkable stability. These results indicated that the ARG solution could be adequately removed on the 2.5D electrode, providing an effective method for wastewater treatment.

Highlights

  • Electrochemical oxidation (EO) is an environmentally friendly technology for treatment of hazardous or refractory contaminants from wastewater [1,2,3,4,5]

  • In the 2.5D electrode system, the titanium tube-based lead dioxide electrode was covered by a certain amount of Sb–SnO2, magnetic powder used as the anode

  • This indicates that the number of electrode surface active sites in 2.5D electrode system was larger than that in the traditional 2D electrode system

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Summary

Introduction

Electrochemical oxidation (EO) is an environmentally friendly technology for treatment of hazardous or refractory contaminants from wastewater [1,2,3,4,5]. The DSA electrodes are are inexpensive, easy to prepare, and have high catalytic properties and strong stability [1,11,17,18]. The PbO2 electrode was a typical titanium-based electrode with excellent stability and high hydroxyl radical yield [29]. The new 2.5D electrode system (as shown in Scheme 1) consists of PbO2 electrode and Sb–SnO2 particles. That combination makes full (as shown in Scheme 1) consists of PbO2 electrode and Sb–SnO2 particles. That combination makes use of the high stability of PbO2 electrode and the high catalytic activity of Sb–SnO2 particles. At the full use of the high stability of PbO2 electrode and the high catalytic activity of Sb–SnO2 particles. The mass transfer and electrochemical performance of this new 2.5D electrode system were investigated in detail, and the electrocatalytic degradation experiments of relevant target organics were conducted

Chemicals and Reagents
Electrode and Magnetic Powder Preparation
Material Characterizations
Determination of Mass Transfer Coefficient
Cyclic Voltammogram Test
Electrochemical Oxidation Process
Toxicity Evaluation of Degradation Result
Mass Transfer Coefficient
Hydroxyl Radicals
Electrochemically Active Site
Electrocatalytic
Effect of Current Density
Effect of factors on degradation by using the
Effect of Initial Organic Concentration
As shown
Effect on ARG
Conclusions

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