过硫酸盐
化学
电子顺磁共振
阿累尼乌斯方程
自旋俘获
声化学
水溶液
动力学
分析化学(期刊)
羟基自由基
活化能
光化学
激进的
物理化学
核磁共振
催化作用
有机化学
物理
量子力学
作者
Zongsu Wei,Frederick A. Villamena,Linda K. Weavers
标识
DOI:10.1021/acs.est.6b05392
摘要
Ultrasound (US) was shown to activate persulfate (PS) providing an alternative activation method to base or heat as an in situ chemical oxidation (ISCO) method. The kinetics and mechanism of ultrasonic activation of PS were examined in aqueous solution using an in situ electron paramagnetic resonance (EPR) spin trapping technique and radical trapping with probe compounds. Using the spin trap, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), hydroxyl radical (•OH) and sulfate radical anion (SO4•-) were measured from ultrasonic activation of persulfate (US-PS). The yield of •OH was up to 1 order of magnitude greater than that of SO4•-. The comparatively high •OH yield was attributed to the hydrolysis of SO4•- in the warm interfacial region of cavitation bubbles formed from US. Using steady-state approximations, the dissociation rate of PS in cavitating bubble systems was determined to be 3 orders of magnitude greater than control experiments without sonication at ambient temperature. From calculations of the interfacial volume surrounding cavitation bubbles and using the Arrhenius equation, an effective mean temperature of 340 K at the bubble-water interface was estimated. Comparative studies using the probe compounds tert-butyl alcohol and nitrobenzene verified the bubble-water interface as the location for PS activation by high temperature with •OH contributing a minor role in activating PS to SO4•-. The mechanisms unveiled in this study provide a basis for optimizing US-PS as an ISCO technology.
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