Field observations of SIV in cloud

被引:8
作者
Cape, JN
McFadyen, GG
Storeton-West, RL
Choularton, TW
Gallagher, MW
Bower, KN
Lee, DS
Dore, C
Berner, A
机构
[1] Inst Terr Ecol, Penicuik EH26 0QB, Midlothian, Scotland
[2] UMIST, Dept Appl Phys, Manchester M60 1QD, Lancs, England
[3] AEA Technol, Abingdon, Oxon, England
[4] Univ Vienna, Inst Expt Phys, A-1090 Vienna, Austria
基金
英国自然环境研究理事会;
关键词
kinetics; peroxide; bisulphite; chemical analysis;
D O I
10.1016/S0169-8095(98)00101-X
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
A novel technique for measuring dissolved sulphur dioxide/bisulphite/sulphite (S-IV) continuously in cloud water has been used in a study of the oxidation of S-IV in a hill cap cloud. In March/April 1995 measurements were made at Great Dun Fell, Cumbria, of the concentrations of gases and particles entering and leaving a hill cap cloud, and of the ions dissolved in the cloud. An approximate sulphur balance was obtained, but the precision was not sufficient to demonstrate sulphate formation under the observed conditions of very low sulphur dioxide (SO2) concentrations (< 1 ppb). However, measurements of SO2 and hydrogen peroxide (H2O2) upwind of the cloud, and of S-IV and H2O2 in cloud water, showed that: (i) in conditions when H2O2 concentrations were small (< 0.1 ppb in the gas phase below cloud), S-IV concentrations in the cloud were consistent with Henry's Law equilibrium (cloud water pH was around 6, with ammonium (NH4+) concentrations over 100 mu M), suggesting negligible loss of S-IV between sampling and analysis; (ii) in the presence of larger concentrations of H2O2 the measured S-IV concentration was much smaller than predicted from solution pH and measured SO, concentrations, but consistent with losses between sampling and analysis caused by reaction with formaldehyde (HCHO) and metal-catalysed oxidation by O-2. Use of the method in future should aim to minimise the time between sampling and analysis of S-IV. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:345 / 358
页数:14
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