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Annmarie G Carlton

Publications and source records attributed to Annmarie G Carlton.

3 recordsLinked to original sources

Evidence for oligomer formation in clouds: reactions of isoprene oxidation products.

Electrospray ionization mass spectrometry (ESI-MS) was used to investigate product formation in laboratory experiments designed to study secondary organic aerosol (SOA) formation in clouds. It has been proposed that water soluble aldehydes derived from aromatics and alkenes, including isoprene, oxidize further in cloud droplets forming organic acids and, upon droplet evaporation, SOA. Pyruvic acid is an important aqueous-phase intermediate. Time series samples from photochemical batch aqueous phase reactions of pyruvic acid and hydrogen peroxide were analyzed for product formation. In addition to the monomers predicted by the reaction scheme, products consistent with an oligomer system were found when pyruvic acid and OH radical were both present. No evidence of oligomer formation was found in a standard mix composed of pyruvic, glyoxylic, and oxalic acids prepared in the same matrix as the samples analyzed using the same instrument conditions. The distribution of high molecular weight products is consistent with oligomers composed of the mono-, oxo-, and di-carboxylic acids expected from the proposed reaction scheme.

Aldehydes↗

Isoprene forms secondary organic aerosol through cloud processing: model simulations.

Isoprene accounts for more than half of non-methane volatile organics globally. Despite extensive experimentation, homogeneous formation of secondary organic aerosol (SOA) from isoprene remains unproven. Herein, an incloud process is identified in which isoprene produces SOA. Interstitial oxidation of isoprene produces water-soluble aldehydes that react in cloud droplets to form organic acids. Upon cloud evaporation new organic particulate matter is formed. Cloud processing of isoprene contributes at least 1.6 Tg yr(-1) to a global biogenic SOA production of 8-40 Tg yr(-1). We conclude that cloud processing of isoprene is an important contributor to SOA production, altering the global distribution of hygroscopic organic aerosol and cloud condensation nuclei.

Aerosols↗

Design of a cost-effective weighing facility for PM2.5 quality assurance.

The U.S. Environmental Protection Agency (EPA) Quality Assurance (QA) Guidance Document 2.12: Monitoring PM2.5 in Ambient Air Using Designated Reference or Class I Equivalent Methods (Document 2.12) requires conditioning of PM2.5 filters at 20-23 degrees C and 30-40% relative humidity (RH) for 24 hr prior to gravimetric analysis. Variability of temperature and humidity may not exceed +/-2 degrees C and +/-5% RH during the conditioning period. The quality assurance team at EPA Region 2's regional laboratory designed a PM2.5 weighing facility that operates well within these strict performance requirements. The traditional approach to meeting the performance requirements of Document 2.12 for PM2.5 filter analysis is to build a walk-in room, with costs typically exceeding $100,000. The initial one-time capital cost for the laboratory at EPA's Edison, NJ, facility was approximately $24,000. Annual costs [e.g., National Institute of Standards and Technology (NIST) recertifications and nitrogen replacement cylinders used for humidity control] are approximately $500. The average 24-hr variabilities in temperature and RH in the Region 2 weighing chamber are small, +/-0.2 degrees C and +/-0.8% RH, respectively. The mass detection limit for the PM2.5 weighing system of 47-mm stretched Teflon (lab blank) filters is 6.3 microg. This facility demonstrates an effective and economical example for states and other organizations planning PM2.5 weighing facilities.

Air Pollutants↗