Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractAttenuation of luteinizing hormone surges in neuropeptide Y knockout mice    Next AbstractCorrigendum: Olfactory perception and behavioral effects of sex pheromone gland components in Helicoverpa armigera and Helicoverpa assulta »

J Hazard Mater


Title:Degradation of carbon tetrachloride in aqueous solution in the thermally activated persulfate system
Author(s):Xu M; Gu X; Lu S; Qiu Z; Sui Q; Miao Z; Zang X; Wu X;
Address:"State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237, China. State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237, China. Electronic address: lvshuguang@ecust.edu.cn"
Journal Title:J Hazard Mater
Year:2015
Volume:20141219
Issue:
Page Number:7 - 14
DOI: 10.1016/j.jhazmat.2014.12.031
ISSN/ISBN:1873-3336 (Electronic) 0304-3894 (Linking)
Abstract:"Thermal activation of persulfate (PS) has been identified to be effective in the destruction of organic pollutants. The feasibility of carbon tetrachloride (CT) degradation in the thermally activated PS system was evaluated. The experimental results showed that CT could be readily degraded at 50 degrees C with a PS concentration of 0.5M, and CT degradation and PS consumption followed the pseudo-first order kinetic model. Superoxide radical anion (O2(*-)) was the predominant radical species responsible for CT degradation and the split of CCl was proposed as the possible reaction pathways for CT degradation. The process of CT degradation was accelerated by higher PS dose and lower initial CT concentration. No obvious effect of the initial pH on the degradation of CT was observed in the thermally activated PS system. Cl(*-), HCO3(*-), and humic acid (HA) had negative effects on CT degradation. In addition, the degradation of CT in the thermally activated PS system could be significantly promoted by the solvents addition to the solution. In conclusion, the thermally activated PS process is a promising option in in-situ chemical oxidation/reduction remediation for degrading highly oxidized organic contaminants such as CT that is widely detected in contaminated sites"
Keywords:"Carbon Tetrachloride/*chemistry Groundwater Hot Temperature Humic Substances Hydrogen-Ion Concentration Kinetics Oxidation-Reduction Oxygen/chemistry Solvents/chemistry Sulfides/*chemistry Superoxides/chemistry Volatile Organic Compounds Water Pollutants, ;"
Notes:"MedlineXu, Minhui Gu, Xiaogang Lu, Shuguang Qiu, Zhaofu Sui, Qian Miao, Zhouwei Zang, Xueke Wu, Xiaoliang eng Research Support, Non-U.S. Gov't Netherlands 2014/12/30 J Hazard Mater. 2015 Apr 9; 286:7-14. doi: 10.1016/j.jhazmat.2014.12.031. Epub 2014 Dec 19"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 01-07-2024