Polychlorinated alkanes in indoor environment: A review of levels, sources, exposure, and health implications for chlorinated paraffin mixtures.

Chemosphere

Department of Physics, Chemistry and Biology (IFM), Linköping University, 581 83, Linköping, Sweden; Department of Thematic Studies - Environmental Change, Linköping University, 581 83, Linköping, Sweden.

Published: October 2024

AI Article Synopsis

  • - Polychlorinated n-alkanes (PCAs), found in chlorinated paraffins categorized by chain length (SCCPs, MCCPs, LCCPs), pose significant health risks due to their persistence and toxic nature in indoor environments.
  • - A lack of standardized terminology and methods makes it tough to compare PCA contamination across studies, highlighting challenges in assessing exposure risks from indoor dust, air, and organic materials.
  • - Key indoor sources of PCA emissions include building materials and household products, with dermal absorption and ingestion as the highest risk pathways for human exposure, influenced by factors such as local legislation, product availability, cleaning habits, and ventilation.

Article Abstract

Polychlorinated n-alkanes (PCAs) are the main components of chlorinated paraffins (CPs) mixtures, that have been commonly grouped into short-chain (SCCPs, C), medium-chain (MCCPs, C), and long-chain (LCCPs, C) CPs. PCAs pose a significant risk to human health as they are broadly present in indoor environments and are potentially persistent, bioaccumulative, and toxic. The lack of specific terminology and harmonization in analytical methodologies for PCA analysis complicates direct comparisons between studies. The present work summarizes the different methodologies applied for the analysis of PCAs in indoor dust, air, and organic films. The large variability between the reviewed studies points to the difficulties to assess PCA contamination in these matrices and to mitigate risks associated with indoor exposure. Based on our review of physicochemical properties of PCAs and previously reported sum of measurable S/M/LCCPs levels, the homologue groups PCAs-C are found to be mostly present in the gas phase, PCAs-C in particulate matter and organic films, and PCAs-C in settled dust. However, we emphasized that mapping PCA sources and distribution in the indoors is highly dependent on the individual homologues. To further comprehend indoor PCA distribution, we described the uses of PCA in building materials and household products to apportion important indoor sources of emissions and pathways for human exposure. The greatest risk for indoor PCAs were estimated to arise from dermal absorption and ingestion through contact with dust and CP containing products. In addition, there are several factors affecting indoor PCA levels and exposure in different regions, including legislation, presence of specific products, cleaning routines, and ventilation frequency. This review provides comprehensive analysis of available indoor PCA data, the physicochemical properties, applied analytical methods, possible interior sources, variables affecting the levels, human exposure to PCAs, as well as need for more information, thereby providing perspectives for future research studies.

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Source
http://dx.doi.org/10.1016/j.chemosphere.2024.143326DOI Listing

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