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Laboratory partitioning experiments were conducted to elucidate the sorption behaviour and partitioning of perfluoroalkyl compounds (PFCs). Three different sediment types were used and separately spiked with perfluorooctanoate (PFOA), perfluorooctane sulfonate (PFOS) and perfluorooctane sulfonamide (PFOSA) at low environmentally realistic concentrations. PFOA, PFOS and PFOSA were mainly distributed in the dissolved phase at low suspended solid concentrations, indicating their long-range transport potential in the marine environment. In all cases, the equilibrium isotherms were linear and the organic carbon normalised partition coefficients (KOC) decreased in the following order: PFOSA (log KOC = 4.1 ± 0.35 cm3 g−1) > PFOS (3.7 ± 0.56 cm3 g−1) > PFOA (2.4 ± 0.12 cm3 g−1). The level of organic content had a significant influence on the partitioning. For the sediment with negligible organic content the density of the sediment became the most important factor influencing the partitioning. Ultimately, data on the partitioning of PFCs between aqueous media and suspended solids are essential for modelling their transport and environmental fate.  相似文献   
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In this study, residual concentrations of chlorpyrifos (CPF) were determined in feed (40) and fodder (25) samples collected from various locations of Tarai region of Uttarakhand. For extracting residues, liquid–liquid partition followed by alumina column clean up was used and the detection and quantification of residues was undertaken with the help of high-performance liquid chromatography using C18 column and diode array detector at 220?nm. Of the total 40 feed samples analyzed, 7 (17.5%) samples were found positive for CPF with the mean residual concentration of 0.058?µg?g?1; while out of 25 fodder samples, CPF residues were detected in a single (4%) sample with residual concentration of 0.39?µg?g?1. However, none of the feed or fodder samples contained CPF residues above the prescribed limit.  相似文献   
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The bioaccumulation of perfluorooctanesulfonamide (PFOSA) and two fluorotelomer alcohols (8:2 FTOH, 10:2 FTOH) by rainbow trout (Oncorhynchus mykiss) through dietary exposure, including depuration rates and metabolism was investigated. Concentrations in the spiked feed ranged from 10.9 μg g−1 wet weight (wet wt) for PFOSA and 6.7 μg g−1 wet wt for 8:2 FTOH to 5.0 μg g−1 wet wt for 10:2 FTOH. Trout was fed at 1.5% body weight per day for 30 d and depuration was followed for up to 30 d following previously published dietary exposure protocols. Perfluorooctanesulfonate (PFOS) was the major perfluoroalkylsulfonate (PFSA) detected in fish following dietary exposure to PFOSA. Half-lives of PFOS and PFOSA were 16.9 ± 2.5 and 6.0 ± 0.4 d, respectively. A biomagnification factor (BMF) of 0.023 was calculated for PFOSA which indicates that dietary exposure to PFOSA does not result in biomagnification in the rainbow trout. PFOS had a BMF of 0.08. The fluorotelomer saturated acids (8:2 FTCA, 10:2 FTCA) and fluorotelomer unsaturated acids (8:2 FTUCA, 10:2 FTUCA) were the major products detected in rainbow trout following dietary exposure to 8:2 FTOH and 10:2 FTOH, respectively. Half-lives were 3.7 ± 0.4, 2.1 ± 0.5, 3.3, and 1.3 d for 10:2 FTCA, 10:2 FTUCA, 8:2 FTCA, and 8:2 FTUCA, respectively. Small amounts of perfluorooctanoate (PFOA) and perfluorodecanoate (PFDA) were also detected in the FTOH exposed fish.  相似文献   
4.
研究了不同培养介质和培养方式下全氟辛烷磺酰胺(PFOSA)在小麦、蚯蚓体内的生物富集和转化.结果表明:小麦根系可以从培养介质中吸收PFOSA并向上转运至茎叶.土壤中PFOSA生物有效性受总有机碳(TOC)的影响显著,高TOC含量土壤中PFOSA的生物有效性降低,导致其在小麦和蚯蚓中的生物富集因子分别由(61.24±8.42)和(21347.91±208.86)降至(5.61±0.23)和(1404.92±108.21).PFOSA在小麦的根和茎叶以及蚯蚓中都可以转化为PFOS,但在蚯蚓中的转化率((3.87±1.71)%)显著低于小麦((26.39±3.02)%).小麦根中PFOS的支链异构体(br-PFOS)比例在低、高TOC含量时分别为(14.8±2.0)%、(66.1±26.2)%,低于茎叶(分别为(63.0±21.3)%、(85.2±2.4)%)),可能是由于根部转化生成的br-PFOS更容易向茎叶转运.小麦特别是小麦茎叶中的br-PFOS比例((85.2±2.4)%)显著高于蚯蚓((16.5±4.0)%).小麦的存在可以提高土壤中PFOSA的生物有效性,从而促进蚯蚓对PFOSA的富集,但对其转化影响不大.本文为小麦和蚯蚓中PFOSA的富集和转化提供了证据,有助于探索环境中PFOS的间接来源.  相似文献   
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