z-logo
open-access-imgOpen Access
Nitrate and oxidized organic ions in single particle mass spectra during the 1999 Atlanta Supersite Project
Author(s) -
Lee ShanHu,
Murphy Daniel M.,
Thomson David S.,
Middlebrook Ann M.
Publication year - 2003
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2001jd001455
Subject(s) - nitrate , sulfate , relative humidity , aerosol , particle (ecology) , ion , analytical chemistry (journal) , environmental chemistry , chemistry , mass spectrum , geology , meteorology , organic chemistry , physics , oceanography
We measured the chemical components of 0.35–2.5 μm diameter aerosols with a Particle Analysis by Laser Mass Spectrometry (PALMS) instrument during the Atlanta Supersite Project in August 1999. This paper presents the results for nitrate and oxidized organics. More than 20% of the negative ion spectra of single particles contained nitrate ion peaks. Nitrate peaks showed a clear maximum during the morning at the time of high ambient relative humidity. Nitrate peaks also had a small local maximum during the afternoon when the gas‐phase HNO 3 concentrations were high. This afternoon maximum was more significant for the particles containing soot/hydrocarbons or aluminosilicate components than for the typical organic/sulfate particles. About 45% of negative spectra contained ions indicative of the oxidized organics. Oxidized organic peaks showed a diurnal variation similar to the nitrate: a morning time maximum during the relative humidity maximum and a small maximum in the afternoon. However, in contrast to the nitrate peaks, the afternoon local maximum of oxidized organic peaks was apparent on the organic/sulfate particles. Both nitrate and oxidized organic peaks had larger ion fractions in particles with higher scattered light intensities.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here