Application of high-resolution time-of-flight chemical ionization mass spectrometry measurements to estimate volatility distributions of α-pinene and naphthalene oxidation products

被引:41
作者
Chhabra, P. S. [1 ]
Lambe, A. T. [1 ,2 ]
Canagaratna, M. R. [1 ]
Stark, H. [1 ,3 ]
Jayne, J. T. [1 ]
Onasch, T. B. [1 ,2 ]
Davidovits, P. [2 ]
Kimmel, J. R. [1 ,3 ,4 ]
Worsnop, D. R. [1 ]
机构
[1] Aerodyne Res Inc, Billerica, MA USA
[2] Boston Coll, Dept Chem, Chestnut Hill, MA 02167 USA
[3] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[4] TOFWERK AG, Thun, Switzerland
基金
美国国家科学基金会;
关键词
SECONDARY ORGANIC AEROSOL; PRESSURE ESTIMATION METHODS; PURE COMPONENT PROPERTIES; VAPOR-PRESSURES; HETEROGENEOUS OXIDATION; INITIATED OXIDATION; PART; GAS; SOA; OH;
D O I
10.5194/amt-8-1-2015
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Recent developments in high-resolution time-of-flight chemical ionization mass spectrometry (HR-ToF-CIMS) have made it possible to directly detect atmospheric organic compounds in real time with high sensitivity and with little or no fragmentation, including low-volatility, highly oxygenated organic vapors that are precursors to secondary organic aerosol formation. Here, using ions identified by high-resolution spectra from an HR-ToF-CIMS with acetate reagent ion chemistry, we develop an algorithm to estimate the vapor pressures of measured organic acids. The algorithm uses identified ion formulas and calculated double bond equivalencies, information unavailable in quadrupole CIMS technology, as constraints for the number of possible oxygen-containing functional groups. The algorithm is tested with acetate chemical ionization mass spectrometry (acetate-CIMS) spectra of O-3 and OH oxidation products of alpha-pinene and naphthalene formed in a flow reactor with integrated OH exposures ranged from 1.2 x 10(11) to 9.7 x 10(11) molec scm(-3), corresponding to approximately 1.0 to 7.5 days of equivalent atmospheric oxidation. Measured gas-phase organic acids are similar to those previously observed in environmental chamber studies. For both precursors, we find that acetate-CIMS spectra capture both functionalization (oxygen addition) and fragmentation (carbon loss) as a function of OH exposure. The level of fragmentation is observed to increase with increased oxidation. The predicted condensed-phase secondary organic aerosol (SOA) average acid yields and O / C and H / C ratios agree within uncertainties with previous chamber and flow reactor measurements and ambient CIMS results. While acetate reagent ion chemistry is used to selectively measure organic acids, in principle this method can be applied to additional reagent ion chemistries depending on the application.
引用
收藏
页码:1 / 18
页数:18
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