甲苯
化学
苯
过氧化氢
芬顿反应
反应机理
过氧化物
转化(遗传学)
光化学
机制(生物学)
催化作用
氧气
羟基自由基
无机化学
有机化学
生物化学
哲学
认识论
基因
作者
Scott G. Huling,Sangchul Hwang,Dennis D. Fine,Saebom Ko
出处
期刊:Water Research
[Elsevier]
日期:2011-10-15
卷期号:45 (16): 5334-5342
被引量:11
标识
DOI:10.1016/j.watres.2011.08.001
摘要
In Fenton-driven oxidation treatment systems, reaction intermediates derived from parent compounds can play a significant role in the overall treatment process. Fenton-like reactions in the presence of toluene or benzene, involved a transformation mechanism that was highly efficient relative to the conventional Fenton-driven mechanism. A delay in hydrogen peroxide (H2O2) reaction occurred until the complete or near-complete transformation of toluene or benzene and involved the simultaneous reaction of dissolved oxygen. This highly efficient transformation mechanism is initiated by Fenton-like reactions, and therefore dependent on conventional Fenton-like parameters. Results indicated that several potential parameters and mechanisms did not play a significant role in the transformation mechanism including electron shuttles, Fe chelates, high valent oxo-iron complexes, anionic interferences in H2O2 reaction, and H2O2 formation. The Fenton-like initiation, formation, and propagation of a reaction intermediate species capable of transforming toluene, while simultaneously inhibiting H2O2 reaction is the most viable mechanism.
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