Cloud condensation nuclei activity of fresh primary and aged biomass burning aerosol

被引:93
|
作者
Engelhart, G. J. [1 ]
Hennigan, C. J. [1 ]
Miracolo, M. A. [1 ]
Robinson, A. L. [1 ]
Pandis, S. N. [1 ,2 ,3 ]
机构
[1] Carnegie Mellon Univ, Ctr Atmospher Particle Studies, Pittsburgh, PA 15217 USA
[2] Univ Patras, Dept Chem Engn, Patras, Greece
[3] Fdn Res & Technol, Inst Chem Engn Sci, Patras, Greece
关键词
ORGANIC AEROSOL; CCN ACTIVITY; HYGROSCOPICITY; ACTIVATION; PARTICLES; SIZE; EMISSIONS; PHOTOOXIDATION; UNCERTAINTIES; DISTRIBUTIONS;
D O I
10.5194/acp-12-7285-2012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We quantify the hygroscopic properties of particles freshly emitted from biomass burning and after several hours of photochemical aging in a smog chamber. Values of the hygroscopicity parameter, kappa, were calculated from cloud condensation nuclei (CCN) measurements of emissions from combustion of 12 biomass fuels commonly burned in North American wildfires. Prior to photochemical aging, the kappa of the fresh primary aerosol varied widely, between 0.06 (weakly hygroscopic) and 0.6 (highly hygroscopic). The hygroscopicity of the primary aerosol was positively correlated with the inorganic mass fraction of the particles. Photochemical processing reduced the range of kappa values to between 0.08 and 0.3. The changes in kappa were driven by the photochemical production of secondary organic aerosol (SOA). SOA also contributed to growth of particles formed during nucleation events. Analysis of the nucleation mode particles enabled the first direct quantification of the hygroscopicity parameter kappa for biomass burning SOA, which was on average 0.11, similar to values observed for biogenic SOA. Although initial CCN activity of biomass burning aerosol emissions are highly variable, after a few hours of photochemical processing kappa converges to a value of 0.2 +/- 0.1. Therefore, photochemical aging reduces the variability of biomass burning CCN kappa, which should simplify analysis of the potential effects of biomass burning aerosol on climate.
引用
收藏
页码:7285 / 7293
页数:9
相关论文
共 50 条
  • [21] Absorption of chemically aged biomass burning carbonaceous aerosol
    Tasoglou, Antonios
    Saliba, Georges
    Subramanian, R.
    Pandis, Spyros N.
    [J]. JOURNAL OF AEROSOL SCIENCE, 2017, 113 : 141 - 152
  • [22] Size distribution and chemical composition of primary particles emitted during open biomass burning processes: Impacts on cloud condensation nuclei activation
    Chen, Li
    Li, Qing
    Wu, Di
    Sun, Hao
    Wei, Yaqi
    Ding, Xiang
    Chen, Hui
    Cheng, Tiantao
    Chen, Jianmin
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2019, 674 : 179 - 188
  • [23] Role of Aerosol Physicochemical Properties on Aerosol Hygroscopicity and Cloud Condensation Nuclei Activity in a Tropical Coastal Atmosphere
    Ajith, T. C.
    Kompalli, Sobhan Kumar
    Babu, S. Suresh
    [J]. ACS EARTH AND SPACE CHEMISTRY, 2022, 6 (06): : 1527 - 1542
  • [24] AEROSOL AND CLOUD CONDENSATION NUCLEI MEASUREMENTS IN THE KUWAIT PLUME
    HUDSON, JG
    CLARKE, AD
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D13) : 14533 - 14536
  • [25] Cloud condensation nuclei from biomass burning during the Amazonian dry-to-wet transition season
    Martins, Jorge Alberto
    Goncalves, Fabio Luiz T.
    Morales, Carlos A.
    Fisch, Gilberto F.
    Pinheiro, Francisco Geraldo M.
    Leal, Joao Bosco V., Jr.
    Oliveira, Carlos J.
    Silva, Emerson M.
    Oliveira, Jose Carlos P.
    Costa, Alexandre A.
    Silva Dias, Maria Assuncao F.
    [J]. METEOROLOGY AND ATMOSPHERIC PHYSICS, 2009, 104 (1-2) : 83 - 93
  • [26] Cloud condensation nuclei from biomass burning during the Amazonian dry-to-wet transition season
    Jorge Alberto Martins
    Fábio Luiz T. Gonçalves
    Carlos A. Morales
    Gilberto F. Fisch
    Francisco Geraldo M. Pinheiro
    João Bosco V. Leal Júnior
    Carlos J. Oliveira
    Emerson M. Silva
    José Carlos P. Oliveira
    Alexandre A. Costa
    Maria Assunção F. Silva Dias
    [J]. Meteorology and Atmospheric Physics, 2009, 104 : 83 - 93
  • [27] Contribution of primary carbonaceous aerosol to cloud condensation nuclei: processes and uncertainties evaluated with a global aerosol microphysics model
    Pierce, J. R.
    Chen, K.
    Adams, P. J.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2007, 7 (20) : 5447 - 5466
  • [28] Laboratory studies of the chemical composition and cloud condensation nuclei (CCN) activity of secondary organic aerosol (SOA) and oxidized primary organic aerosol (OPOA)
    Lambe, A. T.
    Onasch, T. B.
    Massoli, P.
    Croasdale, D. R.
    Wright, J. P.
    Ahern, A. T.
    Williams, L. R.
    Worsnop, D. R.
    Brune, W. H.
    Davidovits, P.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2011, 11 (17) : 8913 - 8928
  • [29] Combustion organic aerosol as cloud condensation nuclei in ship tracks
    Russell, LM
    Noone, KJ
    Ferek, RJ
    Pockalny, RA
    Flagan, RC
    Seinfeld, JH
    [J]. JOURNAL OF THE ATMOSPHERIC SCIENCES, 2000, 57 (16) : 2591 - 2606
  • [30] Global cloud condensation nuclei influenced by carbonaceous combustion aerosol
    Spracklen, D. V.
    Carslaw, K. S.
    Poeschl, U.
    Rap, A.
    Forster, P. M.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2011, 11 (17) : 9067 - 9087