SOLUBILITY OF SINGLE CHEMICAL-COMPOUNDS FROM AN ATMOSPHERIC AEROSOL IN PURE WATER

Citation
P. Hoffmann et al., SOLUBILITY OF SINGLE CHEMICAL-COMPOUNDS FROM AN ATMOSPHERIC AEROSOL IN PURE WATER, Atmospheric environment, 31(17), 1997, pp. 2777-2785
Citations number
34
Categorie Soggetti
Environmental Sciences","Metereology & Atmospheric Sciences
Journal title
ISSN journal
13522310
Volume
31
Issue
17
Year of publication
1997
Pages
2777 - 2785
Database
ISI
SICI code
1352-2310(1997)31:17<2777:SOSCFA>2.0.ZU;2-N
Abstract
The water-solubility differentiates atmospheric particles into cloud c ondensation nuclei (CCN) and interstitial aerosol. This interaction be tween aerosol and cloud influences the climate in different known and hypothetical ways [Hansson et al. (1994) In Proceedings of EUROTRAC Sy mposium'94, (edited by Borrell P. M.), p. 984. SPB Academic Publishing , The Hague; Schwartz et al. (1995) In Aerosol Forcing of Climate (edi ted by Charlson R. J. and Heintzanberg J.), p. 251. Wiley, London]. So me authors studied the fraction of water-soluble amounts with particle size [Meszaros (1968) Tellus 20, 443; Winkler (1974) Meteorol. Rdsch. 27, 129; Fuzzi et al. (1988) Journal of geophysics Research 93, 1114) ; Svenningsson et al. (1992) Tellus 44B, 556; (1994) Journal of Atmosp heric Chemistry 19, 129). As the water-solubility (or hygroscopicity) is a property of chemical compounds it is of great interest to identif y the chemical composition of aerosols and of the dissolved fraction. Using an optimal combination of analytical methods, the elemental and species concentrations were determined in the original aerosol as well as in the resulting solutions. The fraction of soluble species were c alculated from the measured values and three groups were found: with h igh (50-73%), medium (20-26%), and low (2%) dissolved fraction. In a f urther series of experiments the rate constants of dissolution of vari ous species were determined. These can be arranged in the order of dec reasing rate of dissolution: the alkaline and alkaline earth elements K+ approximate to Mg2+ > NH4+ > Na+ > Ca2+, the anions NO3- approximat e to SO42- approximate to Cl-, and for the iron oxidation states Fe3much greater than Fe2+. A photolytic reduction of Fe3+ to Fe2+ was als o observed. For Mg2+, Ca2+, and SO42- a dependance of the rate constan ts for dissolution on time was discovered. This can be explained by th e presence of different chemical compounds in the aerosol. The discuss ion of the results with regard to the time scale of the formation of c loud or fog droplets shows that the slightly soluble inventory of a so lid aerosol of the alkaline and alkaline earth elements, as well as of the anions, is dissolved into the aqueous phase in a relatively short time interval of 10-700 s. On the other hand, Fe3+ is dissolved in a time period of 3000-4500 s, whereas Fe2+ appears in the solution in a time period of up to 7000 s. (C) 1997 Elsevier Science Ltd.