Generation of submicron Arizona test dust aerosol:: Chemical and hygroscopic properties

被引:81
作者
Vlasenko, A
Sjögren, S
Weingartner, E
Gäggeler, HW
Ammann, M [1 ]
机构
[1] Paul Scherrer Inst, Lab Radio & Environm, CH-5232 Villigen, Switzerland
[2] Univ Bern, Dept Chem & Biochem, Bern, Switzerland
[3] Paul Scherrer Inst, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
关键词
D O I
10.1080/027868290959870
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This article describes a submicron dust aerosol generation system based on a commercially available dust disperser intended for use in laboratory studies of heterogeneous gas-aerosol interactions. Mineral dust particles are resuspended from Arizona Test Dust (ATD) powder as a case study. The system output in terms of number and surface area is adjustable and stable enough for aerosol flow reactor studies. Particles produced are in the 30-1000 nm size range with a lognormal shape of the number size distribution. The particles are characterized with respect to morphology, electrical properties, hygroscopic properties, and chemical composition. Sub-micron particle elemental composition is found to be similar for the particle surface and bulk as revealed by X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma optical emission spectroscopy (ICP-OES), respectively. A significant difference in chemical composition is found between the submicron aerosol and the ATD bulk powder from which it was generated. The anionic composition of the water-soluble fraction of this dust sample is dominated by sulfate. Resuspended dust particles show, as expected, nonhygroscopic behavior in a humid environment. Small hygroscopic growth of about 1% (relative change in mobility diameter) was observed for 100 nm particles when the relative humidity (RH) was changed from 12 to 94%. Particles larger than 100-200 nm shrank about 1% once exposed to RH > 90%. This was interpreted as a restructuring of the larger agglomerates of dust to particles of smaller mobility diameter, under the influence of water vapor.
引用
收藏
页码:452 / 460
页数:9
相关论文
共 38 条
[1]   Heterogeneous production of nitrous acid on soot in polluted air masses [J].
Ammann, M ;
Kalberer, M ;
Jost, DT ;
Tobler, L ;
Rössler, E ;
Piguet, D ;
Gäggeler, HW ;
Baltensperger, U .
NATURE, 1998, 395 (6698) :157-160
[2]  
[Anonymous], CLIMATE CHANGE 2001, DOI DOI 10.1088/1748-9326/4/4/045112
[3]  
[Anonymous], 1977, ATMOSPHERIC AEROSOLS
[4]   Global modeling of heterogeneous chemistry on mineral aerosol surfaces: Influence on tropospheric ozone chemistry and comparison to observations [J].
Bauer, SE ;
Balkanski, Y ;
Schulz, M ;
Hauglustaine, DA ;
Dentener, F .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D2)
[5]  
Bian H.S., 2003, J GEOPHYS RES, V108, DOI [DOI 10.1029/2002JD003143, 10.1029/2002JD003143.]
[6]  
BLACKFORD DB, 1986, TIZ FACHBERICHTE, V10, P645
[7]  
BUONICORE AJ, 1992, AIR POLLUTION ENG MA, P912
[8]  
COOPER DW, 2001, METHODS SIZE DISTRIB, P667
[9]   African dust aerosols as atmospheric ice nuclei [J].
DeMott, PJ ;
Sassen, K ;
Poellot, MR ;
Baumgardner, D ;
Rogers, DC ;
Brooks, SD ;
Prenni, AJ ;
Kreidenweis, SM .
GEOPHYSICAL RESEARCH LETTERS, 2003, 30 (14) :ASC1-1
[10]   The pH-dependent dissolution of wind-transported Saharan dust [J].
Desboeufs, KV ;
Losno, R ;
Vimeux, F ;
Cholbi, S .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D17) :21287-21299