Particle-Phase Chemistry of Secondary Organic Material: Modeled Compared to Measured O:C and H:C Elemental Ratios Provide Constraints

被引:133
作者
Chen, Qi [1 ]
Liu, Yingjun [1 ]
Donahue, Neil M. [2 ]
Shilling, John E. [3 ]
Martin, Scot T. [1 ,4 ]
机构
[1] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Carnegie Mellon Univ, Ctr Atmospher Particle Studies, Pittsburgh, PA 15213 USA
[3] Pacific NW Natl Lab, Atmospher Sci & Global Change Div, Richland, WA 99352 USA
[4] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02138 USA
关键词
RESOLUTION MASS-SPECTROMETRY; ALPHA-PINENE OZONOLYSIS; AEROSOL SOA FORMATION; 2ND-GENERATION PRODUCTS; MCM V3; ISOPRENE; OXIDATION; PHOTOOXIDATION; MONOTERPENES; IDENTIFICATION;
D O I
10.1021/es104398s
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Chemical mechanisms for the production of secondary organic material (SOM) are developed in focused laboratory studies but widely used in the complex modeling context of the atmosphere. Given this extrapolation, a stringent testing of the mechanisms is important. In addition to particle mass yield as a typical standard for model-measurement comparison, particle composition expressed as O:C and H:C elemental ratios can serve as a higher dimensional constraint. A paradigm for doing so is developed herein for SOM production from a C-5-C-10-C-15 terpene sequence, namely isoprene, a-pinene, and beta-caryopyhllene. The model MCM-SIMPOL is introduced based on the Master Chemical Mechanism (MCM v3.2) and a group contribution method for vapor pressures (SIMPOL). The O:C and H:C ratios of the SOM are measured using an Aerosol Mass Spectrometer (AMS). Detailed SOM-specific AMS calibrations for the organic contribution to the H2O+ and CO+ ions indicate that published O:C and H:C ratios for SOM are systematically too low. Overall, the measurement-model gap was small for particle mass yield but significant for particle-average elemental composition. The implication is that a key chemical pathway is missing from the chemical mechanism. The data can be explained by the particle-phase homolytic decomposition of organic hydroperoxides and subsequent alkyl-radical-promoted oligomerization.
引用
收藏
页码:4763 / 4770
页数:8
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