Indoor air concentrations of PM2.5 quartz fiber filter-collected ionic PFAS and emissions to outdoor air: findings from the IPA campaign.

IF 4.3 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL Environmental Science: Processes & Impacts Pub Date : 2024-10-03 DOI:10.1039/d4em00359d
Naomi Y Chang, Clara M A Eichler, Daniel E Amparo, Jiaqi Zhou, Karsten Baumann, Elaine A Cohen Hubal, Jason D Surratt, Glenn C Morrison, Barbara J Turpin
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Abstract

Per- and polyfluoroalkyl substances (PFAS) are prevalent in consumer products used indoors. However, few measurements of ionic PFAS exist for indoor air. We analyzed samples collected on PM2.5 quartz fiber filters (QFFs) in 11 North Carolina homes 1-3 times in living rooms (two QFFs in series), and immediately outside each home (single QFF), for 26 ionic PFAS as part of the 9 months Indoor PFAS Assessment (IPA) Campaign. All targeted PFAS, except for PFDS and 8:2 monoPAP, were detected indoors. PFBA, PFHpA, PFHxA, PFOA, PFOS, and 6:2 diPAP were detected in >50% of indoor samples. PFHxA, PFOA, and PFOS had the highest detection frequency (DF = 80%; medians = 0.5-0.7 pg m-3), while median PFBA concentrations (3.6 pg m-3; DF = 67%) were highest indoors. Residential indoor air concentrations (sum of measured PFAS) were, on average, 3.4 times higher than residential outdoor air concentrations, and an order of magnitude higher than regional background concentrations. Indoor-to-outdoor emission rate estimates suggest that emissions from single unit homes could be a meaningful contributor to PFBA, PFOA, and PFOS emissions in populated areas far from major point sources. Backup QFFs were observed to adsorb some targeted PFAS from the gas-phase, making reported values upper-bounds for particle-phase and lower-bounds for total air (gas plus particle) concentrations. We found that higher concentrations of carbonaceous aerosol were associated with a shift in partitioning of short chain PFCAs and long chain PFSAs toward the particle phase.

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室内空气中 PM2.5 石英纤维过滤器收集的离子型全氟辛烷磺酸浓度以及向室外空气中的排放:IPA 运动的发现。
全氟和多氟烷基物质 (PFAS) 在室内使用的消费品中非常普遍。然而,对室内空气中离子型 PFAS 的测量却很少。作为为期 9 个月的 "室内全氟辛烷磺酸评估 (IPA) 运动 "的一部分,我们在北卡罗来纳州的 11 个家庭中,通过 PM2.5 石英纤维过滤器 (QFF) 对客厅(两个 QFF 串联)和每个家庭外(单个 QFF)的 26 种离子型全氟辛烷磺酸样本进行了 1-3 次分析。除全氟辛烷磺酸和 8:2 单羟基萘外,室内检测到了所有目标全氟辛烷磺酸。在超过 50% 的室内样本中检测到了 PFBA、PFHpA、PFHxA、PFOA、PFOS 和 6:2 diPAP。PFHxA、PFOA 和 PFOS 的检测频率最高(DF = 80%;中位数 = 0.5-0.7 pg m-3),而 PFBA 的浓度中位数(3.6 pg m-3;DF = 67%)在室内最高。住宅室内空气浓度(测得的 PFAS 总和)平均是住宅室外空气浓度的 3.4 倍,比区域背景浓度高出一个数量级。室内到室外的排放率估算表明,在远离主要点源的人口密集地区,单个单元住宅的排放可能是 PFBA、PFOA 和 PFOS 排放的重要来源。据观察,后备 QFF 可吸附气相中的某些目标 PFAS,从而使报告值成为颗粒相浓度的上限和总空气(气体加颗粒)浓度的下限。我们发现,碳质气溶胶浓度较高时,短链全氟辛烷磺酸和长链全氟辛烷磺酸会向颗粒相转移。
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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
期刊最新文献
Finding non-fluorinated alternatives to fluorinated gases used as refrigerants. Indoor air concentrations of PM2.5 quartz fiber filter-collected ionic PFAS and emissions to outdoor air: findings from the IPA campaign. Associations of indoor airborne microbiome with lung function: evidence from a randomized, double-blind, crossover study of microbial intervention. Physicochemical properties and their impact on ice nucleation efficiency of respiratory viral RNA and proteins. Improved prediction of PFAS partitioning with PPLFERs and QSPRs.
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