Sorption of pharmaceuticals and personal care products to polyethylene debris

被引:338
作者
Wu, Chenxi [1 ]
Zhang, Kai [1 ,2 ]
Huang, Xiaolong [1 ,2 ]
Liu, Jiantong [1 ]
机构
[1] Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Donghu South Rd 7, Wuhan 430072, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Microplastics; PPCPs; Sorption; Hydrophobic interaction; Salinity; Dissolved organicmatter; DISSOLVED ORGANIC-MATTER; PLASTIC DEBRIS; MARINE-SEDIMENTS; TRACE-METALS; MICROPLASTICS; ACCUMULATION; ENVIRONMENT; SHORELINES; POLLUTANTS; BEHAVIORS;
D O I
10.1007/s11356-016-6121-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Presence of plastic debris in marine and freshwater ecosystems is increasingly reported. Previous research suggested plastic debris had a strong affiliation for many pollutants, such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and heavy metals. In this study, the sorption behavior of pharmaceuticals and personal care products (PPCPs), including carbamazepine (CBZ), 4-methylbenzylidene camphor (4MBC), triclosan (TCS), and 17 alpha-ethinyl estradiol (EE2), to polyethylene (PE) debris (250 to 280 mu m) was investigated. The estimated linear sorption coefficients (K-d) are 191.4, 311.5, 5140, and 53,225 L/kg for CBZ, EE2, TCS, and 4MBC, and are related to their hydrophobicities. Increase of salinity from 0.05 to 3.5 % did not affect the sorption of 4MBC, CBZ, and EE2 but enhanced the sorption of TCS, likely due to the salting-out effect. Increase of dissolved organic matter (DOM) content using Aldrich humic acid (HA) as a proxy reduced the sorption of 4MBC, EE2, and TCS, all of which show a relatively strong affiliation to HA. Results from this work suggest that microplastics may play an important role in the fate and transport of PPCPs, especially for those hydrophobic ones.
引用
收藏
页码:8819 / 8826
页数:8
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