Direct observation of completely processed calcium carbonate dust particles

被引:165
作者
Laskin, A
Iedema, MJ
Ichkovich, A
Graber, ER
Taraniuk, I
Rudich, Y
机构
[1] Pacific NW Natl Lab, William R Wiley Environm Mol Sci Lab, Richland, WA 99352 USA
[2] Weizmann Inst Sci, Dept Environm Sci, IL-76100 Rehovot, Israel
[3] Agr Res Org, Volcani Ctr, Inst Soil Water & Environm Sci, IL-50250 Bet Dagan, Israel
关键词
D O I
10.1039/b417366j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study presents, for the first time, field evidence of complete, irreversible processing of solid calcium carbonate (calcite)-containing particles and quantitative formation of liquid calcium nitrate particles apparently as a result of heterogeneous reaction of calcium carbonate-containing mineral dust particles with gaseous nitric acid. Formation of nitrates from individual calcite and sea salt particles was followed as a function of time in aerosol samples collected at Shoresh, Israel. Morphology and compositional changes of individual particles were observed using conventional scanning electron microscopy with energy dispersive analysis of X-rays (SEM/EDX) and computer controlled SEM/EDX. Environmental scanning electron microscopy (ESEM) was utilized to determine and demonstrate the hygroscopic behavior of calcium nitrate particles found in some of the samples. Calcium nitrate particles are exceptionally hygroscopic and deliquesce even at very low relative humidity (RH) of 9-11 % which is lower than typical atmospheric environments. Transformation of non-hygroscopic dry mineral dust particles into hygroscopic wet aerosol may have substantial impacts on light scattering properties, the ability to modify clouds and heterogeneous chemistry.
引用
收藏
页码:453 / 468
页数:16
相关论文
共 88 条
[1]  
[Anonymous], GEN AEROSOLS
[2]  
ARMSTRONG JT, 1991, ELECTRON PROBE QUANTITATION, P261
[3]   Minerals in the air:: An environmental perspective [J].
Buseck, PR ;
Jacob, DJ ;
Pósfai, M ;
Li, J ;
Anderson, JR .
INTERNATIONAL GEOLOGY REVIEW, 2000, 42 (07) :577-593
[4]   Non-sea-salt-sulphate formation in sea-salt aerosol [J].
Clegg, NA ;
Toumi, R .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D23) :31095-31102
[5]   INTRODUCTION TO THE ESEM INSTRUMENT [J].
DANILATOS, GD .
MICROSCOPY RESEARCH AND TECHNIQUE, 1993, 25 (5-6) :354-361
[6]   Single particle analysis of aerosols, observed in the marine boundary layer during the Monterey Area Ship Tracks Experiment (MAST), with respect to cloud droplet formation [J].
De Bock, LA ;
Joos, PE ;
Noone, KJ ;
Pockalny, RA ;
Van Grieken, RE .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2000, 37 (03) :299-329
[7]   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
[8]   Measurements of the concentration and composition of nuclei for cirrus formation [J].
DeMott, PJ ;
Cziczo, DJ ;
Prenni, AJ ;
Murphy, DM ;
Kreidenweis, SM ;
Thomson, DS ;
Borys, R ;
Rogers, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :14655-14660
[9]   Role of mineral aerosol as a reactive surface in the global troposphere [J].
Dentener, FJ ;
Carmichael, GR ;
Zhang, Y ;
Lelieveld, J ;
Crutzen, PJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D17) :22869-22889
[10]   The impact of aerosols on solar ultraviolet radiation and photochemical smog [J].
Dickerson, RR ;
Kondragunta, S ;
Stenchikov, G ;
Civerolo, KL ;
Doddridge, BG ;
Holben, BN .
SCIENCE, 1997, 278 (5339) :827-830