Measurements comparison of oxygenated volatile organic compounds at a rural site during the 1995 SOS Nashville Intensive

被引:27
作者
Apel, EC
Calvert, JG
Riemer, D
Pos, W
Zika, R
Kleindienst, TE
Lonneman, WA
Fung, K
Fujita, E
Shepson, PB
Starn, TK
Roberts, PT
机构
[1] Natl Ctr Atmospher Res, Boulder, CO 80307 USA
[2] Univ Miami, Rosenstiel Sch Marine & Atmospher Sci, Miami, FL 33149 USA
[3] ManTech Environm, Atmospher Chem Grp, Res Triangle Pk, NC 27709 USA
[4] US EPA, Natl Environm Res Lab, Res Triangle Pk, NC 27711 USA
[5] AtmAA, Calabasas, CA 91302 USA
[6] Univ Nevada, Desert Res Inst, Energy & Environm Engn Ctr, Reno, NV 89506 USA
[7] Purdue Univ, W Lafayette, IN 47907 USA
[8] Sonoma Technol Inc, Santa Rosa, CA 95403 USA
关键词
D O I
10.1029/98JD01753
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Simultaneous measurements of oxygenated volatile organic compounds (OVOCs) by four independent research groups at the Youth Incorporated (YI) site during the 1995 Southern Oxidants Study Nashville Intensive, between July 4 and 30, 1995, provided a unique opportunity to compare results from different techniques. 2,4-Dinitrophenylhydrazine (DNPH) coated C18 (C18(AtmAA)) and Si-Gel (Si-Gel(MTE)) cartridges were compared with each other and with two sorbent-based preconcentration gas chromatographic (GC) techniques coupled with mass spectrometric (MS) detection (GC/MSUM and GC/MSPU) or flame ionization detection GC/FIDUM. The experiment consisted of both a laboratory (part A) and an ambient air comparison (part B). In part A of the study, standard mixtures of OVOCs were diluted in a flowing gas stream of humidified, purified air, both with and without addition of O3, and distributed to participant's instrumentation. Concentrations were compared with the expected values based on known cylinder concentrations and dilution factors. In part B of the study, the instruments sampled ambient air from a common glass manifold. Species intercompared were formaldehyde, acetaldehyde, acetone, and propanal. The C18(AtmAA) data were typically higher than the Si-GelMTE data for the four intercompared compounds, and possible explanations are given. Agreement between the cartridge systems and the GC/MS, GC/FID systems for comeasured compounds was poorer than expected but improved towards the end of the experiment. The GC/MS systems tracked each other well for acetone, but there were differences in the absolute concentration values. These results show that improvements in the accuracy and comparability of techniques should be of high priority.
引用
收藏
页码:22295 / 22316
页数:22
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