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Insight into the interaction of tetrabromobisphenol A with sediment-derived dissolved organic carbon in a multiphase system by direct immersion solid phase microextraction

四溴双酚A 化学 固相微萃取 吸附 吸附 溶解有机碳 离子强度 环境化学 分配系数 沉积物 色谱法 阻燃剂 水溶液 质谱法 有机化学 气相色谱-质谱法 地质学 古生物学
作者
Xiaohui Zhu,Liangzhong Li,Zhenyu Lu,Junyan Zhu,Lun Lu,Zhengdong Wang,Mingdeng Xiang,Guining Lu,Zhi Dang,Yunjiang Yu
出处
期刊:Science of The Total Environment [Elsevier]
卷期号:912: 169037-169037
标识
DOI:10.1016/j.scitotenv.2023.169037
摘要

Tetrabromobisphenol A (TBBPA), a ubiquitously used commercial brominated flame retardant (BFR), has been widely detected in aquatic environments, and has aroused much attention due to its potential adverse effects on aquatic organisms. However, current research on the environmental fate and transport of TBBPA in the sediment–dissolved organic carbon (DOC)–water polyphase system is lacking. In this study, the sorption behavior of TBBPA in a water–DOC–sediment system was investigated using the direct-immersion solid-phase microextraction (DI-SPME) method, and the free dissolved concentration (Cw-SPME) and DOC adsorption concentration (CDOC) of TBBPA in water were measured by applying this DI-SPME approach. In addition, the effects of pH, ionic strength, and soluble organic concentration on the adsorption of TBBPA in the multiphase system were evaluated. The adsorption kinetics experimental results show that the adsorption behavior of TBBPA on sediments conforms to a linear model, suggesting that it could be mainly absorbed by sediments. The solid–water partition coefficient (Kd) of TBBPA was artificially reduced 1.54 times using the traditional liquid–liquid extraction method because the sorption behavior of the DOC was ignored, which could be accurately corrected using the DI-SPME method. The logKd and logKOC of TBBPA in the multiphase system were 4.12 ± 0.25 and 6.48 ± 0.25, respectively. Finally, the interference experiment revealed that the sorption behavior of TBBPA was affected by the pH, ionic strength (calcium ion), and humic acid concentration, apart from the lead ion concentration itself.

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