(263d) Identification and Characterization of Semivolatile Organic Carbon Using Proton Transfer Reaction - Mass Spectrometry (Ptr-MS) | AIChE

(263d) Identification and Characterization of Semivolatile Organic Carbon Using Proton Transfer Reaction - Mass Spectrometry (Ptr-MS)

Authors 

Presto, A. A. - Presenter, Carnegie Mellon University
Huff Hartz, K. E., Carnegie Mellon University
Donahue, N. M., Carnegie Mellon University


We present an analysis of volatile and semivolatile species produced during monoterpene oxidation using proton transfer reaction - mass spectrometry (PTR-MS). Partitioning theory dictates that atmospheric organic species with finite saturation vapor pressures must exist in both the gas and aerosol phases. Such species are typically defined as semivolatile, and a number of semivolatile species, particularly monoterpene oxidation products, have been identified using filter-based methods. However, the relative abundances of these semivolatile products in the gas and aerosol phases has not been investigated previously. The high time resolution of the PTR-MS allows us to investigate changes in organic concentrations on the order of a few minutes; this time resolution starkly contrasts filter-based measurements, which may take hours to collect.

Secondary organic aerosol (SOA) is generated in an environmental chamber by the ozonolysis of a monoterpene precursor (typically alpha-pinene or limonene) in the presence of an OH radical scavenger. The particle mass and number distributions are measured with an SMPS, and organic concentrations are monitored using PTR-MS. Species identified with PTR-MS are consistent with results from filter-based measurements, and include limononaldehyde, 7-hydroxy-limononaldehyde, and 7-hydroxy-keto-limononaldehyde from limonene ozonolysis, and pinonaldeyhde, norpinonaldehyde, norpinonic acid, and pinonic acid from alpha-pinene ozonolysis.

Additionally, PTR-MS allows us to investigate the differences between dark chamber experiments conducted in the absence of NOx with experiments conducted in high-NOx environments or in the presence of UV light. We have previously observed that the gas-phase conditions (i.e., NOx concentration) can significantly affect SOA yield. Filter-based measurements allow little insight into the underlying gas-phase chemistry that controls SOA yield. The higher time resolution (and low detection limit) of the PTR-MS allows for the investigation of changes in organic speciation both during and after terpene consumption.