4.5 Article

An in situ gas chromatograph with automatic detector switching between PTR- and EI-TOF-MS: isomer-resolved measurements of indoor air

Journal

ATMOSPHERIC MEASUREMENT TECHNIQUES
Volume 14, Issue 1, Pages 133-152

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/amt-14-133-2021

Keywords

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Funding

  1. Alfred P. Sloan Foundation [G-2016-7173, G-2019-12444]

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The study presents a field-deployable gas chromatograph with thermal desorption preconcentration for in situ measurements of volatile organic compounds. The system demonstrated fast time-response data acquisition, molecular speciation, and high-resolution mass spectral information for each resolved GC peak. Results show successful identification and quantification of a range of VOCs in indoor environments, suggesting the production of DMSD from humidity-dependent heterogeneous reactions on surfaces.
We have developed a field-deployable gas chromatograph (GC) with thermal desorption preconcentration (TDPC), which is demonstrated here with automatic detector switching between two high-resolution time-of-flight mass spectrometers (TOF-MSs) for in situ measurements of volatile organic compounds (VOCs). This system provides many analytical advances, including acquisition of fast time-response data in tandem with molecular speciation and two types of mass spectral information for each resolved GC peak: molecular ion identification from Vocus proton transfer reaction (PTR) TOF-MS and fragmentation pattern from electron ionization (EI) TOF-MS detection. This system was deployed during the 2018 ATHLETIC campaign at the University of Colorado Dal Ward Athletic Center in Boulder, Colorado, where it was used to characterize VOC emissions in the indoor environment. The addition of the TDPC-GC increased the Vocus sensitivity by a factor of 50 due to preconcentration over a 6min GC sample time versus direct air sampling with the Vocus, which was operated with a time resolution of 1 Hz. The GC-TOF methods demonstrated average limits of detection of 1.6 ppt across a range of monoterpenes and aromatics. Here, we describe the method to use the two-detector system to conclusively identify a range of VOCs including hydrocarbons, oxygenates, and halocarbons, along with detailed results including the quantification of anthropogenic monoterpenes, where limonene accounted for 47%-80% of the indoor monoterpene composition. We also report the detection of dimethylsilanediol (DMSD), an organosiloxane degradation product, which was observed with dynamic temporal behavior distinct from volatile organosiloxanes (e.g., decamethylcyclopentasiloxane, D5 siloxane). Our results suggest DMSD is produced from humidity-dependent heterogeneous reactions occurring on surfaces in the indoor environment, rather than formed through gas-phase oxidation of volatile siloxanes.

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