Monolithic Porous Magnéli-phase Ti₄O₇ for Electro-oxidation Treatment of Industrial Wastewater

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• 作者：Shijie You^a ; ^{sjyou@hit.edu.cn" class="auth_mail" title="E-mail the corresponding author} ; Bo Liu^a ; Yifan Gao^a ; Yu Wang^a ; Chuyang Y. Tang^b ; ^{tangc@hku.hk" class="auth_mail" title="E-mail the corresponding author} ; Yibing Huang^c ; Nanqi Ren^a
• 关键词：Magné ; li-phase Ti4O7 electrode ; Electrochemical oxidation ; Dyeing and finishing wastewater
• 刊名：Electrochimica Acta
• 出版年：2016
• 出版时间：1 October 2016
• 年：2016
• 卷：214
• 期：Complete
• 页码：326-335
• 全文大小：1441 K

文摘

Electrochemical oxidation (EO) processes have been gaining a growing popularity in wastewater treatment. Their engineered applications inspire the search for conductive, stable, inexpensive, and sustainable electrode materials. Magnéli-phase titanium oxides have unique crystal and electron structure, which result in good electrical conductivity approaching that of metal and excellent corrosion resistance close to that of ceramics. We fabricated a monolithic porous Magnéli-phase Ti₄O₇ electrode for EO of refractory industrial dyeing and finishing wastewater (DFWW). The results demonstrated that the electrochemically active area of porous Ti₄O₇ electrode was 2–3 orders of magnitude higher than the apparent surface area of bulk electrode. The Ti₄O₇ electrode achieved efficient and stable abatement of recalcitrant organic pollutants on site without any extra addition of chemicals. The soluble chemical oxygen demand (COD) and dissolved organic carbon (DOC) were removed by 66.5% and 46.7%, respectively, at current density of 8 mA cm⁻² after 2 h reaction. The bioavailability of treated wastewater was improved substantially, indicated by one order of magnitude increase in BOD₅/COD. The Ti₄O₇ electrode had good long-term stability, with its maximum COD removal declined only slightly (<8%) at current density of 20 mA cm⁻² during a 50-cycle operation. The organic pollutants appear most likely to be oxidized by electrochemically generated active species like physisorbed OH radical and aqueous ClO⁻ species under mass transfer control condition. The current study provides important insights for achieving efficient and sustainable electrochemical wastewater treatment using the novel porous Ti₄O₇ electrode material.