
Real-Time Measurements of Gas-Phase Medium-Chain Chlorinated Paraffins Reveal Daily Changes in Gas-Particle Partitioning Controlled by Ambient Temperature
Daniel John Katz, Bri Dobson, Mitchell Alton, Harald Stark, Douglas R. Worsnop, Manjula R. Canagaratna, and Eleanor C. Brown
ACS Environmental Au
ACS Environ. Au 2025
Publication Date: June 5, 2025
https://doi.org/10.1021/acsenvironau.5c00038
© 2025 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.
Abstract.
Chlorinated paraffins (CPs) are synthetic polychlorinated n-alkanes produced as mixtures of a range of CxClyH2x–y+2 formulas. CPs have numerous industrial applications but are toxic, long-lived, and environmentally ubiquitous with environmental releases occurring throughout their production, use, and disposal. Short-chain chlorinated paraffins (SCCPs, C10–13) have been regulated by the United States Environmental Protection Agency since 2009 and by the Stockholm Convention since 2017. SCCP regulation is expected to cause increased production of medium-chain chlorinated paraffins (MCCPs; C14–17), which are currently under consideration for Stockholm Convention regulations. Thus, there is a need to improve the understanding of MCCP environmental transport, distribution, and fate. Existing measurements are limited in their spatial and temporal coverage. Measurements of CP atmospheric loading are particularly scarce. Historically, these measurements have required long sampling times, obscuring the temporal behavior of atmospheric CPs. We report real-time in situ measurements of 18 gas-phase MCCPs. These measurements were made in the United States Southern Great Plains with nitrate ion chemical ionization mass spectrometry (NO3–CIMS). The estimated average lower-limit concentration of MCCPs is on the order of single-digit ng/m3. MCCP diel behavior is partially explained by gas-particle partitioning with implications for MCCP transport and lifetimes.