Optimization of a low flow sampler for improved assessment of gas and particle bound exposure to chlorinated paraffins.

Chemosphere

NILU-Norwegian Institute for Air Research, Fram Centre, NO-9296, Tromsø, Norway; UiT-The Arctic University of Norway, Department of Arctic and Marine Biology, Hansine Hansens Veg 18, 9037, Tromsø, Norway. Electronic address:

Published: July 2021

An optimized low volume sampler was developed to determine both gas- and particle bound concentrations of short and medium-chain chlorinated paraffins (S/MCCPs). Background contamination was limited by the sampler design, providing method quantification limits (MQLs) at least two orders of magnitude lower than other studies within the gas (MQL: 500 pg (ΣSCCPs), 1.86 ng (ΣMCCPs)) and particle (MQL: 500 pg (ΣSCCPs), 1.72 ng (ΣMCCPs) phases. Good repeatability was observed between parallel indoor measurements (RSD ≤ 9.3% (gas), RSD ≤ 14% (particle)) with no breakthrough/saturation observed after a week of continuous sampling. For indoor air sampling, SCCPs were dominant within the gas phase (17 ± 4.9 ng/m) compared to MCCPs (2.7 ± 0.8 ng/m) while the opposite was observed in the particle bound fraction (0.28 ± 0.11 ng/m (ΣSCCPs) vs. 2.7 ± 1.0 ng/m (ΣMCCPs)). Only SCCPs in the gas phase could be detected reliably during outdoor sampling and were considerably lower compared to indoor concentrations (0.27 ± 0.10 ng/m). Separation of the gas and particle bound phase was found to be crucial in applying the appropriate response factors for quantification based on the deconvoluted S/MCCP sample profile, thus avoiding over- (gas phase) or underestimation (particle phase) of reported concentrations. Very short chain chlorinated paraffins (vSCCPs, C-C) were also detected at equal or higher abundance compared to SCCP congener groups (C-C) congener groups, indicating an additional human indoor inhalation risk.

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http://dx.doi.org/10.1016/j.chemosphere.2021.130066DOI Listing

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