A Detailed Reaction Mechanism for Thiosulfate Oxidation by Ozone in Aqueous Environments

被引:1
|
作者
Deal, Alexandra M. [1 ]
Prophet, Alexander M. [1 ,2 ]
Bernal, Franky [1 ,2 ]
Saykally, Richard J. [1 ,2 ]
Wilson, Kevin R. [1 ]
机构
[1] Lawrence Berkeley Natl Lab, Chem Sci Div, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
mining effluent; remediation; atmosphericaerosols; ozonation; polythionates; sulfuroxyanions; pH dependence; VALENCE SULFUR-COMPOUNDS; CHEMICAL BEHAVIOR; DITHIONITE ION; DECOMPOSITION; KINETICS; TETRATHIONATE; AEROSOL; WATER; TRITHIONATE; INTERFACES;
D O I
10.1021/acs.est.4c06188
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The ozone oxidation, or ozonation, of thiosulfate is an important reaction for wastewater processing, where it is used for remediation of mining effluents, and for studying aerosol chemistry, where its fast reaction rate makes it an excellent model reaction. Although thiosulfate ozonation has been studied since the 1950s, challenges remain in developing a realistic reaction mechanism that can satisfactorily account for all observed products with a sequence of elementary reaction steps. Here, we present novel measurements using trapped microdroplets to study the pH-dependent thiosulfate ozonation kinetics. We detect known products and intermediates, including SO32-, SO42-, S3O62-, and S4O62-, establishing agreement with the literature. However, we identify S2O42- as a new reaction intermediate and find that the currently accepted mechanism does not directly explain observed pH effects. Thus, we develop a new mechanism, which incorporates S2O42- as an intermediate and uses elementary steps to explain the pH dependence of thiosulfate ozonation. The proposed mechanism is tested using a kinetic model benchmarked to the experiments presented here, then compared to literature data. We demonstrate good agreement between the proposed thiosulfate ozonation mechanism and experiments, suggesting that the insights in this paper can be leveraged in wastewater treatment and in understanding potential climate impacts.
引用
收藏
页码:18959 / 18968
页数:10
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