Oxidation of benzoic acid by heat-activated persulfate: Effect of temperature on transformation pathway and product distribution

被引:186
|
作者
Zrinyi, Nick [1 ]
Pham, Anh Le-Tuan [1 ]
机构
[1] Carleton Univ, Dept Civil & Environm Engn, Ottawa, ON K1S 5B6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Heat-activated persulfate; Soil and groundwater treatment; Advanced oxidation process; SITU CHEMICAL OXIDATION; HYDROXYL RADICALS; RATE CONSTANTS; MN(IV)-CONTAINING OXIDES; AQUIFER MATERIALS; AQUEOUS-SOLUTION; WATER; MECHANISM; SULFATE; PEROXYDISULFATE;
D O I
10.1016/j.watres.2017.04.066
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heat activates persulfate (S2O82-) into sulfate radical (SO4 center dot-), a powerful oxidant capable of transforming a wide variety of contaminants. Previous studies have shown that an increase in temperature accelerates the rates of persulfate activation and contaminant transformation. However, few studies have considered the effect of temperature on contaminant transformation pathway. The objective of this study was to determine how temperature (T = 22-70 degrees C) influences the activation of persulfate, the transformation of benzoic acid (i.e., a model compound), and the distribution of benzoic acid oxidation products. The time-concentration profiles of the products suggest that benzoic acid was transformed via decarboxylation and hydroxylation mechanisms, with the former becoming increasingly important at elevated temperatures. The pathway through which the products were further oxidized was also influenced by the temperature of persulfate activation. Our findings suggest that the role of temperature in the persulfate-based treatment systems is not limited only to controlling the rates of sulfate and hydroxyl radical generation. The ability of sulfate radical to initiate decarboxylation reactions and, more broadly, fragmentation reactions, as well as the effect of temperature on these transformation pathways could be important to the transformation of a number of organic contaminants. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:43 / 51
页数:9
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