Gas-Microjet Reactive Scattering: Collisions of HCl and DCl with Cool Salty Water

被引:18
作者
Faust, Jennifer A. [1 ]
Sobyra, Thomas B. [1 ]
Nathanson, Gilbert M. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-BEAM; AQUEOUS-SOLUTIONS; LIQUID GLYCEROL; SURFACE; DISSOCIATION; DYNAMICS; CATION; HBR; EVAPORATION; EXCHANGE;
D O I
10.1021/acs.jpclett.5b02848
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
Liquid microjets provide a powerful means to investigate reactions of gases with salty water in vacuum while minimizing gas-vapor collisions. We use this technique to explore the fate of gaseous HCl and DCl molecules impinging on 8 molal LiCl and LiBr solutions at 238 K. The experiments reveal that HCl or DCl evaporate infrequently if they become thermally accommodated at the surface of either solution. In particular, we observe minimal thermal desorption of HCl following HCl collisions and no distinct evidence for rapid, interfacial DCl -> HCl exchange following DCl collisions. These results imply that surface thermal motions are not generally strong enough to propel momentarily trapped HCl or DCl back into the gas phase before they ionize and disappear into solution. Instead, only HCl and DCl molecules that scatter directly from the surface escape entry. These recoiling molecules transfer less energy upon collision to LiBr/H2O than to LiCl/H2O, reflecting the heavier mass of Br- than of Cl- in the interfacial region.
引用
收藏
页码:730 / 735
页数:6
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