Oxidation mechanism of ammonia in water clusters

被引:0
|
作者
Acosta, Yanitza [1 ]
Gerber, R. Benny [2 ,3 ,4 ]
Varner, Mychel E. [1 ]
机构
[1] Iona Coll, Chem & Biochem Dept, New Rochelle, NY 10801 USA
[2] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
[3] Hebrew Univ Jerusalem, Dept Phys Chem, Jerusalem, Israel
[4] Hebrew Univ Jerusalem, Fritz Haber Res Ctr, Jerusalem, Israel
基金
美国国家科学基金会; 以色列科学基金会;
关键词
Ammonia oxidation; amidogen radical; solvation; MOLECULAR-ORBITAL METHODS; GAUSSIAN-TYPE BASIS; AB-INITIO; RATE CONSTANTS; BASIS-SETS; NH2; OH; RADICALS; DYNAMICS; KINETICS;
D O I
10.1080/00268976.2021.1983057
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
Oxidation of ammonia is an important atmospheric process, but detailed mechanisms are for the most part yet unknown. Here the later steps in a mechanism forming nitric oxide and water from NH2 and O-2 are studied. The transition states for isomerisation of NH2OO to HNOOH and for dissociation of HNOOH to HNO and OH are identified and the subsequent formation of nitric oxide and water is discussed. This process is studied in small water clusters to model the effect of the nearest neighbouring water molecules in larger clusters or at extended surfaces, demonstrating the effect of solvation in lowering the barrier height for NH2OO to HNOOH isomerisation. Proton transfer through the surrounding water provides a feasible reaction path in this system. As a result, it is shown that the high barrier for isomerisation between intermediates in the gas phase is not likely to prevent ammonia oxidation in small water clusters or aerosols.
引用
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页数:6
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