Thermodynamic characterization of Mexico City aerosol during MILAGRO 2006

被引:100
作者
Fountoukis, C. [1 ]
Nenes, A. [1 ,2 ]
Sullivan, A. [2 ]
Weber, R. [2 ]
Van Reken, T. [3 ]
Fischer, M. [4 ]
Matias, E. [5 ]
Moya, M. [5 ]
Farmer, D. [6 ]
Cohen, R. C. [6 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[3] Natl Ctr Atmospher Res, Boulder, CO 80307 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
[5] Univ Nacl Autonoma Mexico, Ctr Ciencias Atmosfera, Mexico City 04510, DF, Mexico
[6] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
AMMONIUM-NITRATE; MCMA-2003; CAMPAIGN; EQUILIBRIUM MODEL; PEROXY NITRATES; ORGANIC AEROSOL; ALKYL NITRATES; GAS; CENICA; HNO3; NO2;
D O I
10.5194/acp-9-2141-2009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fast measurements of aerosol and gas-phase constituents coupled with the ISORROPIA-II thermodynamic equilibrium model are used to study the partitioning of semivolatile inorganic species and phase state of Mexico City aerosol sampled at the T1 site during the MILAGRO 2006 campaign. Overall, predicted semivolatile partitioning agrees well with measurements. PM2.5 is insensitive to changes in ammonia but is to acidic semivolatile species. For particle sizes up to 1 mu m diameter, semi-volatile partitioning requires 15-30 min to equilibrate; longer time is typically required during the night and early morning hours. Aerosol and gas-phase speciation always exhibits substantial temporal variability, so that aerosol composition measurements (bulk or size-resolved) obtained over large integration periods are not reflective of its true state. When the aerosol sulfate-to-nitrate molar ratio is less than unity, predictions improve substantially if the aerosol is assumed to follow the deliquescent phase diagram. Treating crustal species as "equivalent sodium" (rather than explicitly) in the thermodynamic equilibrium calculations introduces important biases in predicted aerosol water uptake, nitrate and ammonium; neglecting crustals further increases errors dramatically. This suggests that explicitly considering crustals in the thermodynamic calculations is required to accurately predict the partitioning and phase state of aerosols.
引用
收藏
页码:2141 / 2156
页数:16
相关论文
共 38 条
[1]   A new inorganic atmospheric aerosol phase equilibrium model (UHAERO) [J].
Amundson, NR ;
Caboussat, A ;
He, JW ;
Martynenko, AV ;
Savarin, VB ;
Seinfeld, JH ;
Yoo, KY .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2006, 6 :975-992
[2]  
[Anonymous], 2007, ATMOS CHEM PHYS, DOI DOI 10.5194/ACPD-7-11257-2007
[3]   Prediction of multicomponent inorganic atmospheric aerosol behavior [J].
Ansari, AS ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (05) :745-757
[4]   The effect of metastable equilibrium states on the partitioning of nitrate between the gas and aerosol phases [J].
Ansari, AS ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (01) :157-168
[5]   An analysis of four models predicting the partitioning of semivolatile inorganic aerosol components [J].
Ansari, AS ;
Pandis, SN .
AEROSOL SCIENCE AND TECHNOLOGY, 1999, 31 (2-3) :129-153
[6]  
Capaldo KP, 2000, ATMOS ENVIRON, V34, P3617
[7]   The effect of dioctyl phthalate films on the ammonium nitrate aerosol evaporation rate [J].
Cruz, CN ;
Dassios, KG ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (23) :3897-3905
[8]   The mass accommodation coefficient of ammonium nitrate aerosol [J].
Dassios, KG ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (18) :2993-3003
[9]   A thermal dissociation laser-induced fluorescence instrument for in situ detection of NO2, peroxy nitrates, alkyl nitrates, and HNO3 -: art. no. 4046 [J].
Day, DA ;
Wooldridge, PJ ;
Dillon, MB ;
Thornton, JA ;
Cohen, RC .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D5-6)
[10]   The T1-T2 study: evolution of aerosol properties downwind of Mexico City [J].
Doran, J. C. ;
Barnard, J. C. ;
Arnott, W. P. ;
Cary, R. ;
Coulter, R. ;
Fast, J. D. ;
Kassianov, E. I. ;
Kleinman, L. ;
Laulainen, N. S. ;
Martin, T. ;
Paredes-Miranda, G. ;
Pekour, M. S. ;
Shaw, W. J. ;
Smith, D. F. ;
Springston, S. R. ;
Yu, X. -Y. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2007, 7 (06) :1585-1598