Characterization and acid-mobilization study of iron-containing mineral dust source materials.

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TitleCharacterization and acid-mobilization study of iron-containing mineral dust source materials.
Publication TypeJournal Article
Year of Publication2008
JournalJournal of Geophysical Research, [Atmospheres]
Volume113
IssueD5
PaginationD05202/1-D05202/18
AuthorsCwiertny, David M., Jonas Baltrusaitis, Gordon J. Hunter, Alexander Laskin, Michelle M. Scherer, and Vicki H. Grassian
PublisherAmerican Geophysical Union
Keywordsiron mineral dust source material acid mobilization
Abstract

Processes that solubilize iron in mineral dust aerosol may increase the amt. of iron supplied to ocean surface waters, and thereby stimulate phytoplankton productivity. In particular, the uptake of acids such as H2SO4 and HNO3 on mineral dust surfaces can produce extremely acidic environments that promote iron dissoln. Here, four samples that represent source materials for mineral dust (Saudi Beach sand (SB), Inland Saudi sand (IS), Saharan Sand (SS) and China Loess (CL)) and one com. ref. material (Arizona Test Dust (AZTD)) were characterized, and examd. in dissoln. studies in solns. of sulfuric, nitric and hydrochloric acid ranging from pH 1 to 3. Mossbauer spectroscopy revealed Fe(III) in all samples, whereas SB, CL and AZTD also contained appreciable Fe(II). Spectra suggest that both Fe(II) and Fe(III) were substituted into aluminosilicates, although CL, AZTD and IS also contained Fe(III) oxide phases. Total iron soly. measured after 24 h ranged between 4-16% of the initial iron content for each material, but did not scale with either the sp. surface area or the total iron content of the samples. Instead, we show that Fe(II)-contg. solid phases such as Fe(II)-substituted aluminosilicates represent a significant, and sometimes dominant, source of sol. Fe in acidic environments. Results of dissoln. studies also show that the nature of the acid influences iron solubilization, as elevated concns. of nitrate encountered from nitric acid at pH 1 suppressed Fe(II) formation. We propose a surface-mediated, non-photochem. redox reaction between nitrate and Fe(II), which may contribute to Fe(II)/Fe(III) cycling in the atm. [on SciFinder(R)]