生物炭
零价铁
过硫酸盐
环境化学
降级(电信)
污染
化学
砜
二甲基亚砜
动力学
核化学
无机化学
吸附
催化作用
热解
有机化学
生物
生态学
电信
物理
量子力学
计算机科学
作者
Wenwen Gong,Dandan He,Xiao Wang,Yuting Yan,Dionysios D. Dionysiou,Lee Blaney,Guilong Peng
标识
DOI:10.1016/j.cej.2024.150553
摘要
In this paper, Fe(IV) was analyzed in the zero-valent iron biochar (ZVI-BC) activated persulfate (PS) process with methyl phenyl sulfoxide (PMSO) as the probe compound. Without a reaction terminator, PMSO degradation continued during the sample holding time, resulting in significant errors in the kinetics analysis. When 1 mM NaNO2, 1 mM NH2OH, 10 mM Na2S2O3, or 10 mM dimethyl sulfoxide were used as terminators, the concentrations of PMSO and its oxidation product, methyl phenyl sulfone (PMSO2), were effectively maintained without changes during the sample holding period. Furthermore, the terminators did not interfere with PMSO or PMSO2 analysis by high performance liquid chromatography. In addition to Fe(IV), free radical (i.e., SO4−, OH, O2−) and nonradical (i.e., 1O2) reactive species were also involved in the ZVI-BC/PS system; however, Fe(IV) was the predominant reactive species. Organic contaminants with electron-donating moieties rapidly reacted with Fe(IV), and the relative contribution of Fe(IV) to overall contaminant degradation decreased as the solution pH was increased. Overall, this study provided new insights into the quantitative analysis of Fe(IV) in the ZVI-BC/PS system and its application to treatment of organic contaminants in solutions with variable water quality.
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