Scavenging efficiency of 'aerosol carbon' and sulfate in supercooled clouds at Mt. Sonnblick (3106 m a.s.l., Austria)

被引:39
作者
Kasper-Giebl, A
Koch, A
Hitzenberger, R
Puxbaum, H
机构
[1] Vienna Tech Univ, Inst Analyt Chem, A-1060 Vienna, Austria
[2] Univ Vienna, Inst Expt Phys, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
scavenging efficiency; total carbon; aerosol carbon; sulfate; liquid water content; cloud water;
D O I
10.1023/A:1006250508562
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cloud water and interstitial aerosol samples collected at Mt. Sonnblick (SBO) were analyzed for sulfate and 'aerosol carbon' to calculate in-cloud scavenging efficiencies. Scavenging efficiencies for sulfate (epsilon(SO4)) ranged from 0.52 to 0.99 with an average of 0.80. 'Aerosol carbon' was scavenged less efficiently with an average value (epsilon(AC)) of 0.45 and minimum and maximum values of 0.14 and 0.81, respectively. Both epsilon(SO) and epsilon(AC) showed a marked, but slightly different, dependence on the liquid water content (LWC) of the cloud. At low LWC, epsilon(SO) increased with rising LWC until it reached a relatively constant value of 0.83 above an LWC of approximate to 0.3 g/m(3). In the case of 'aerosol carbon', we obtained a more gradual increase of epsilon(AC) up to an LWC of approximate to 0.5 g/m(3). At higher LWCs, epsilon(AC) remained relatively constant at 0.60. As the differences between epsilon(SO) and epsilon(A) varied across the LWC range observed at SBO, we assume that part of the `aerosol carbon' was incorporated into the cloud droplets independently from sulfate. This hypothesis is supported by size classified aerosol measurements. The differences in the size distributions of sulfate and total carbon point to a partially external mixture. Thus, the different chemical nature and the differences in the size and mixing state of the aerosol particles are the most likely candidates for the differences in the scavenging behavior.
引用
收藏
页码:33 / 46
页数:14
相关论文
共 31 条
[1]   SAMPLING OF CARBONACEOUS PARTICLES IN THE ATMOSPHERE .2. [J].
APPEL, BR ;
CHENG, W ;
SALAYMEH, F .
ATMOSPHERIC ENVIRONMENT, 1989, 23 (10) :2167-2175
[2]  
BERNER A, 1984, AEROSOLS SCI TECHNOL, P139
[3]  
BRANTNER B, 1994, WATER AIR SOIL POLL, V74, P363
[4]   PROBLEMS IN THE SAMPLING AND ANALYSIS OF CARBON PARTICULATE [J].
CADLE, SH ;
GROBLICKI, PJ ;
MULAWA, PA .
ATMOSPHERIC ENVIRONMENT, 1983, 17 (03) :593-600
[5]   The Great Dun Fell Cloud Experiment 1993: An overview [J].
Choularton, TW ;
Colvile, RN ;
Bower, KN ;
Gallagher, MW ;
Wells, M ;
Beswick, KM ;
Arends, BG ;
Mols, JJ ;
Kos, GPA ;
Fuzzi, S ;
Lind, JA ;
Orsi, G ;
Facchini, MC ;
Laj, P ;
Gieray, R ;
Wieser, P ;
Engelhardt, T ;
Berner, A ;
Kruisz, C ;
Moller, D ;
Acker, K ;
Wieprecht, W ;
Luttke, J ;
Levsen, K ;
Bizjak, M ;
Hansson, HC ;
Cederfelt, SI ;
Frank, G ;
Mentes, B ;
Martinsson, B ;
Orsini, D ;
Svenningsson, B ;
Swietlicki, E ;
Wiedensohler, A ;
Noone, KJ ;
Pahl, S ;
Winkler, P ;
Seyffer, E ;
Helas, G ;
Jaeschke, W ;
Georgii, HW ;
Wobrock, W ;
Preiss, M ;
Maser, R ;
Schell, D ;
Dollard, G ;
Jones, B ;
Davies, T ;
Sedlak, DL ;
David, MM .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (16) :2393-2405
[6]   PHYSICAL FACTORS INFLUENCING WINTER PRECIPITATION CHEMISTRY [J].
COLLETT, JL ;
PREVOT, ASH ;
STAEHELIN, J ;
WALDVOGEL, A .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (04) :782-788
[7]   MEASUREMENTS OF THE CHEMICAL-COMPOSITION OF STRATIFORM CLOUDS [J].
DAUM, PH ;
KELLY, TJ ;
SCHWARTZ, SE ;
NEWMAN, L .
ATMOSPHERIC ENVIRONMENT, 1984, 18 (12) :2671-2684
[8]   A MULTIPLE-SYSTEM, MULTICHANNEL DIFFUSION DENUDER SAMPLER FOR THE DETERMINATION OF FINE-PARTICULATE ORGANIC MATERIAL IN THE ATMOSPHERE [J].
EATOUGH, DJ ;
WADSWORTH, A ;
EATOUGH, DA ;
CRAWFORD, JW ;
HANSEN, LD ;
LEWIS, EA .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (08) :1213-1219
[9]   Phase partitioning of aerosol constituents in cloud based on single-particle and bulk analysis [J].
Gieray, R ;
Wieser, P ;
Engelhardt, T ;
Swietlicki, E ;
Hansson, HC ;
Mentes, B ;
Orsini, D ;
Martinsson, B ;
Svenningsson, B ;
Noone, KJ ;
Heintzenberg, J .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (16) :2491-2502
[10]  
GROLLERT C, 1999, IN PRESS WATER AIR S