Abstract

A new cathodic material for electro-Fenton (EF) process was prepared based on a macroscopic fiber (CNTF) made of mm long carbon nanotubes directly spun from the gas phase by floating catalyst CVD, on a carbon fiber (CF) substrate. CNTF@CF electrode is a highly graphitic material combining a high surface area (~ 260 m2/g) with high electrical conductivity and electrochemical stability . One kind of azo dye, acid orange 7 (AO7), was used as model bio-refractory pollutant to be treated at CNTF@CF cathode in acidic aqueous medium (pH 3.0). The experimental results pointed out that AO7 and its organic intermediate compounds were totally mineralized by hydroxyl radical generated from Fenton reaction. In fact, 96.7 % of the initial TOC was eliminated in 8h of electrolysis by applying a current of -25 mA and ferrous ions as catalyst at concentration of 0.2 mM. At the same electrolysis time, only 23.7 % of TOC removal found on CF support which proved the high mineralization efficiency of new material thanks to CNTs deposition. The CNTF@CF cathode maintained stable its activity during five experimental cycles of EF set-up. The results indicated that CNTF@CF material could be a potential choice for wastewater treatment containing bio-refractory by electrochemical advanced oxidation processes (EAOPs).

Highlights

  • Urban industrial operation has long been identified as a major cause of environmental contaminations through atmospheric deposition and wastewater discharge

  • The increase of total organic carbon (TOC) removal on both carbon fiber (CF) and carbon nanotube fiber (CNTF)@CF cathode was explained by the oxidation of acid orange 7 (AO7) and its intermediate by-products by hydroxyl radicals generated via Eq 1 between H2O2 and Fe2+ catalyst

  • The CNTF@CF was fabricated for the first time as cathodic material to remove the azo dye (AO7) by EF treatment from acid aqueous solution

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Summary

Introduction

Urban industrial operation has long been identified as a major cause of environmental contaminations through atmospheric deposition and wastewater discharge. The mineralization efficiency was monitored by measuring the TOC removal from initial period to several treatment times at 2, 4, 6, and 8 h, respectively. The increase of TOC removal on both CF and CNTF@CF cathode was explained by the oxidation of AO7 and its intermediate by-products by hydroxyl radicals generated via Eq 1 between H2O2 and Fe2+ catalyst.

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