Identification of Emerging Per- and Polyfluoroalkyl Substances (PFAS) in E-waste Recycling Practices and New Precursors for Trifluoroacetic Acid

被引:11
作者
Baqar, Mujtaba [1 ,2 ]
Zhao, Maosen [1 ]
Saleem, Rimsha [2 ]
Cheng, Zhipeng [1 ]
Fang, Bo [1 ]
Dong, Xiaoyu [1 ]
Chen, Hao [1 ]
Yao, Yiming [1 ]
Sun, Hongwen [1 ]
机构
[1] Nankai Univ, Coll Environm Sci & Engn, MOE Key Lab Pollut Proc & Environm Criteria, Tianjin 300350, Peoples R China
[2] Govt Coll Univ, Sustainable Dev Study Ctr, Lahore 54000, Pakistan
基金
中国国家自然科学基金;
关键词
high-resolution mass spectrometry (HRMS); e-waste; emerging PFAS; hazardous recycling; precursorsof TFA; TOP assay; PERFLUOROALKYL ACIDS; WATER; DEGRADATION; FATE;
D O I
10.1021/acs.est.4c05646
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electronic waste is an emerging source of per- and polyfluoroalkyl substance (PFAS) emissions to the environment, yet the contribution from hazardous recycling practices in the South Asian region remains unclear. This study detected 41 PFAS in soil samples from e-waste recycling sites in Pakistan and the total concentrations were 7.43-367 ng/g dry weight (dw) (median: 37.7 ng/g dw). Trifluoroacetic acid (TFA) and 6:2 fluorotelomer sulfonic acid emerged as the dominant PFAS, constituting 49% and 13% of the total PFAS concentrations, respectively. Notably, nine CF3-containing emerging PFAS were identified by the high-resolution mass spectrometry (HRMS)-based screening. Specifically, hexafluoroisopropanol and bistriflimide (NTf2) were consistently identified across all the samples, with quantified concentrations reaching up to 854 and 90 ng/g dw, respectively. This suggests their potential association with electronic manufacturing and recycling processes. Furthermore, except for NTf2, all the identified emerging PFAS were confirmed as precursors of TFA with molar yields of 8.87-40.0% by the TOP assay validation in Milli-Q water. Overall, this study reveals significant emission of PFAS from hazardous e-waste recycling practices and emphasizes the identification of emerging sources of TFA from precursor transformation, which are essential for PFAS risk assessment.
引用
收藏
页码:16153 / 16163
页数:11
相关论文
共 74 条
[1]  
[Anonymous], SHODEX JJ 50 2D RSPA
[2]  
[Anonymous], 2021, Multi-Industry Per- and Polyfluoroalkyl Substances (PFAS) Study - 2021 Preliminary Report
[3]  
[Anonymous], 2019, UNOSEK Proposal
[4]  
Balde C. P., 2015, GLOBAL E WASTE MONIT
[5]  
Balde C. P., 2017, GLOBALE WASTE MONITO
[6]   Combustion of high-calorific industrial waste in conventional brick kilns: An emerging source of PFAS emissions to agricultural soils [J].
Baqar, Mujtaba ;
Saleem, Rimsha ;
Zhao, Maosen ;
Zhao, Leicheng ;
Cheng, Zhipeng ;
Chen, Hao ;
Yao, Yiming ;
Sun, Hongwen .
SCIENCE OF THE TOTAL ENVIRONMENT, 2024, 906
[7]   Discovery and Implications of C2 and C3 Perfluoroalkyl Sulfonates in Aqueous Film-Forming Foams and Groundwater [J].
Barzen-Hanson, Krista A. ;
Field, Jennifer A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY LETTERS, 2015, 2 (04) :95-99
[8]   Screening for perfluoroalkyl acids in consumer products, building materials and wastes [J].
Becanova, Jitka ;
Melymuk, Lisa ;
Vojta, Simon ;
Komprdova, Klara ;
Klanova, Jana .
CHEMOSPHERE, 2016, 164 :322-329
[9]   Challenges in the analytical determination of ultra-short-chain perfluoroalkyl acids and implications for environmental and human health [J].
Bjornsdotter, Maria K. ;
Yeung, Leo W. Y. ;
Karrman, Anna ;
Jogsten, Ingrid Ericson .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2020, 412 (20) :4785-4796
[10]   Atmospheric Degradation of Ozone Depleting Substances, Their Substitutes, and Related Species [J].
Burkholder, James B. ;
Cox, R. A. ;
Ravishankara, A. R. .
CHEMICAL REVIEWS, 2015, 115 (10) :3704-3759