Liquid-Gas Interface of Iron Aqueous Solutions and FentonReagents

被引:10
作者
Gladich, Ivan [3 ]
Chen, Shuzhen [1 ,4 ]
Yang, Huanyu [1 ,4 ]
Boucly, Anthony [1 ]
Winter, Bernd [5 ]
van Bokhoven, Jeroen A. [2 ,6 ]
Ammann, Markus [1 ,4 ]
Artiglia, Luca [1 ,2 ]
机构
[1] Paul Scherrer Inst, Lab Environm Chem, CH-5232 Villigen, Switzerland
[2] Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, Switzerland
[3] European Ctr Living Technol ECLT, I-30123 Venice, Italy
[4] Swiss Fed Inst Technol, Inst Atmospher & Climate Sci, CH-8092 Zurich, Switzerland
[5] Fritz Haber Inst Max Planck Gesell, Mol Phys Dept, D-14195 Berlin, Germany
[6] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8092 Zurich, Switzerland
关键词
MOLECULAR-DYNAMICS; HYDROGEN-PEROXIDE; FENTON OXIDATION; FERRYL ION; C-H; PHOTOEMISSION; FILMS; WATER; DEGRADATION; ACTIVATION;
D O I
10.1021/acs.jpclett.2c00380
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fenton chemistry, involving the reaction between Fe2+and hydrogen peroxide,is well-known due to its applications in the mineralization of extremely stable molecules.Different mechanisms, influenced by the reaction conditions and the solvation sphere of ironions, influence the fate of such reactions. Despite the huge amount of effort spent investigatingsuch processes, a complete understanding is still lacking. This work combines photoelectronspectroscopy and theoretical calculations to investigate the solvation and reactivity of Fe2+andFe3+ions in aqueous solutions. The reaction with hydrogen peroxide, both in homogeneousFenton reagents and at the liquid-vapor interface, illustrates that both ions are homogeneouslydistributed in solutions and exhibit an asymmetric octahedral coordination to water in the caseof Fe2+. No indications of differences in the reaction mechanism between the liquid-vaporinterface and the bulk of the solutions have been found, suggesting that Fe3+and hydroxylradicals are the only intermediates.
引用
收藏
页码:2994 / 3001
页数:8
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