Investigations of the diurnal cycle and mixing state of oxalic acid in individual particles in Asian aerosol outflow. Sullivan, R., C. & Prather, K., A. Environmental Science & Technology, 41(23):8062-8069, 2007. abstract bibtex The mixing state of oxalic acid was measured in Asian outflow during ACE-Asia by direct shipboard measurements using an ATOFMS single-particle mass spectrometer. Oxalic and malonic acids were found to-be predominantly internally mixed with mineral dust and aged sea salt particles. A persistent diurnal cycle of oxalic acid in mineral dust occurred for over 25 days in marine, polluted marine, and dust storm air masses. The preferential enrichment of diacids in mineral dust over carbonaceous particles and their diurnal behavior indicate a photochemical source of the diacids. Oxalate was only detected simultaneously with elevated aged dust particle counts. This suggests that the diurnal production of diacids most likely results from episodic atmospheric processing of the polluted dust aerosol. We propose a mechanism to explain these observations in which the photochemical oxidation of volatile organic compounds is followed by partitioning of the diacids and precursors to the alkaline Asian dust, with subsequent heterogeneous and aqueous oxidation. Our data indicate that the particulate diacids were produced over just a few hours close to the source; no significant production or destruction appears to have occurred during long-range transport to the ship. No evidence of extensive cloud processing of the sampled aerosol was found. This mixing state of diacids has important implications for the solubility and cloud nucleation properties of the dominant fraction of water-soluble organics and the bioavailability of iron in dust.
@article{
title = {Investigations of the diurnal cycle and mixing state of oxalic acid in individual particles in Asian aerosol outflow},
type = {article},
year = {2007},
keywords = {Particulate dicarboxylic-acids,atmosphere,atofms,chemistry,climate,dicarbonyls,dust,long-range transport,mechanisms,organic aerosol},
pages = {8062-8069},
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abstract = {The mixing state of oxalic acid was measured in Asian outflow during ACE-Asia by direct shipboard measurements using an ATOFMS single-particle mass spectrometer. Oxalic and malonic acids were found to-be predominantly internally mixed with mineral dust and aged sea salt particles. A persistent diurnal cycle of oxalic acid in mineral dust occurred for over 25 days in marine, polluted marine, and dust storm air masses. The preferential enrichment of diacids in mineral dust over carbonaceous particles and their diurnal behavior indicate a photochemical source of the diacids. Oxalate was only detected simultaneously with elevated aged dust particle counts. This suggests that the diurnal production of diacids most likely results from episodic atmospheric processing of the polluted dust aerosol. We propose a mechanism to explain these observations in which the photochemical oxidation of volatile organic compounds is followed by partitioning of the diacids and precursors to the alkaline Asian dust, with subsequent heterogeneous and aqueous oxidation. Our data indicate that the particulate diacids were produced over just a few hours close to the source; no significant production or destruction appears to have occurred during long-range transport to the ship. No evidence of extensive cloud processing of the sampled aerosol was found. This mixing state of diacids has important implications for the solubility and cloud nucleation properties of the dominant fraction of water-soluble organics and the bioavailability of iron in dust.},
bibtype = {article},
author = {Sullivan, R. C. and Prather, Kimberly A},
journal = {Environmental Science & Technology},
number = {23}
}
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