Degradation of 4-Nitrophenol from industrial wastewater by nano catalytic Ozonation

Author(s):
Abstract:
In this project, a nano catalyst (TiO2) and ozone combined with each other and they were used for the removal of 4-nitrophenol (4NP) from industrial wastewater. The effect of some operational parameters such as initial pH (3-9), the concentration of pollutant (20-80 mg/L), and amount of TiO2 were investigated. In O3/TiO2 process, the anion radical ( was formed before the production of hydroxyl radical. These results were different from the Ozonation process alone, in which high pH had a positive effect on the degradation of 4NP, because hydroxyl radicals was formed. In ozonation and O3/TiO2 processes, about 89 and 97% of 4NP were degraded respectively, at optimum pH and 60 min of reaction. In catalytic ozonation the degradation rate of 4NP was higher at weak acidic pH conditions (pH=5). The removal of chemical oxygen demand (COD) was increased from 49% (only ozonation) to 74% (O3/TiO2) at 90 min of reaction. The kinetic of degradation was pseudo-first-order and degradation and mineralization of 4NP were estimated by HPLC and COD tests, respectively.
Language:
English
Published:
International Journal of Nano Dimension, Volume:7 Issue: 2, Spring 2016
Pages:
160 to 167
magiran.com/p1548402  
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!