Office of Research and Development Publications

FORMATION OF POLYKETONES IN IRRADIATED TOLUENE/PROPYLENE/NOX/AIR MIXTURES

Citation:

Edney, E O., D J. Driscoll, W S. Weathers, T. E. Kleindienst, T. S. Conver, C. D. McIver, AND W. Li. FORMATION OF POLYKETONES IN IRRADIATED TOLUENE/PROPYLENE/NOX/AIR MIXTURES. AEROSOL SCIENCE AND TECHNOLOGY 35(6):998-1008, (2001).

Impact/Purpose:

1. Determine the secondary organic aerosol (SOA) yields of biogenic and aromatic hydrocarbons under real world concentration and relative humidity conditions.

2. Determine the organic composition of SOA from photooxidation of biogenic and aromatic compounds.

3. Measure the partitioning coefficients of atmospherically relevant semivolatile SOA.

4. Investigate the impact of the chemical composition of the organic fraction of the PM2.5 on the partitioning of SOA compounds.

5. Develop a first generation SOA chemistry module.

Description:

A laboratory study was carried out to investigate the formation of polyketones in secondary organic aerosol from photooxidation of the aromatic hydrocarbon toluene, a major constituent of automobile exhaust. The laboratory experiments consisted of irradiating toluene/propylene/NOx/air mixtures in a smog chamber operated in the dynamic mode and collecting submicron secondary organic aerosol samples on ZefluorTM filters and on stainless steel disks in a low pressure cascade impactor. Carbonyl oxidation products in methanol extracts of the filters were derivatized using O-(2,3,4,5,6,-pentafluorobenzyl)-hydroxylamine and the oxime derivatives were detected with a positive chemical ionization gas chromatography ion trap mass spectroscopy (GC-ITMS) system. Infrared spectra of the cascade impactor samples were used to determine the chemical functional group concentrations of the aerosol. The results of the GC-ITMS and infrared spectral analyses were consistent with the formation of multi-functional oxygenates, including hydroxy diones as well as triones, tetraones and pentaones.

The U.S. Environmental Protection Agency through its Office of Research and Development funded and collaborated in the research described here under Contract 68-D5-0049 to ManTech Environmental Technology, Inc. It has been subject to Agency review and approved for publication. Mention of trade names or commercial products does not constitute an endorsement or recommendation for use.

Record Details:

Record Type:DOCUMENT( JOURNAL/ PEER REVIEWED JOURNAL)
Product Published Date:12/01/2001
Record Last Revised:12/22/2005
Record ID: 65327