Investigation of Dye Removal Efficiency of the Photoelectrocatalytic System Using Graphite and Stainless Steel as Electrodes

Abstract:
The removal of Acid Orange 7 by the photoelectrocatalytic process was investigated at ambient temperature under solar irradiation using graphite as the cathode and stainless steel coated with the ZnO/TiO2 nanocomposite as the anode. The microstructure of the ZnO/TiO2 coated electrode was characterized by the SEM test. The results revealed dye and COD removal efficiencies of 99% and 97%, respectively, over a period of 360 minutes. The best performance was achieved in 360 minutes with no aeration at a current of 1 mA/cm2, an initial dye concentration of 100 mg/L, an electrode surface area of 30 cm2, and an electrolyte concentration of 0.01 M; energy consumption under these optimum conditions was 0.15 KWh/ppm. It may be concluded that the photoelectrocatalytic process is well capable of removing organic compounds, especially textile effluents containing dyes and non-degradable contaminants, due to its ability to produce hydroxyl radicals, superoxide, etc. Thus, the technique may be recommended for use as a pre-treatment process to reduce operational costs.
Language:
Persian
Published:
Journal of Water & Wastewater, Volume:27 Issue: 104, 2016
Pages:
26 to 35
magiran.com/p1543919  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!