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1.
Environ Sci Pollut Res Int ; 29(21): 31659-31674, 2022 May.
Artigo em Inglês | MEDLINE | ID: mdl-35006562

RESUMO

A membrane of triolein-embedded cellulose acetate membrane (TECAM), as an integrative passive sampler, was applied to adsorb 28 polychlorinated biphenyls (PCBs) from pure water and sea water in order to probe into the influence of concentration fluctuation and water matrix. The results demonstrated the temporal variations of PCBs concentrations in TECAM followed the first-order kinetics model. The periodic refreshment of solution and matrix effects of sea water significantly prolonged the time that PCBs reached equilibrium stage. The refreshment facilitated the uptake mass in TECAM. On the contrary, the matrix effects of sea water and dissolved organic matter (DOM) declined the PCBs absorption to TECAM. The average logKP values of PCBs in pure water were about 1.2 log unit higher than those in sea water in the experiments that the solution was not refreshed, while the difference of average logKP values narrowed to 0.3 log unit if the PCBs solutions were periodically refreshed. The correlation between logKP and logKOW values fitted the quadratic curve well, which was similar to semi-permeable membrane device (SPMD). The appropriate sampling times (t94%) ranged from 98.8 to 819 h (mean 500 h) for pure water with refreshment, much longer than those in sea water with refreshment (80.1~410 h, mean 189 h). The t94% values in the solution with high DOM content increased significantly, up to 409 h. Furthermore,  comparing the two experiments that the spiked pure water and sea water solution were refreshed frequently, the estimated sampling rates (Rs) in pure water (0.154~2.06 L/day with a mean value of 0.605 L/day) were slightly lower than those in sea water (0.292~3.84 L/day with a mean value of 1.69 L/day). However, the Rs values in sea water with DOM declined sharply to 0.042 L/day. Therefore, concentration fluctuation, matrix effect, and DOM contents of sea water evidently posed significant influence on dynamic parameters of TECAM absorption, which would be screened and probed detailed in future.


Assuntos
Bifenilos Policlorados , Poluentes Químicos da Água , Celulose/análogos & derivados , Matéria Orgânica Dissolvida , Monitoramento Ambiental/métodos , Trioleína , Água , Poluentes Químicos da Água/análise
2.
Sci Total Environ ; 798: 148985, 2021 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-34329931

RESUMO

Bisphenol analogues (BPs) are emerging contaminants that have been widely detected in water environments. The presence of substituted hydrophilic and hydrophobic groups in the molecule may lead to unclear performance in passive sampling. This study tested the accumulation capacity and passive sampling of fifteen BPs in a triolein-embedded cellulose acetate membrane (TECAM) passive sampler. In a dynamic accumulation experiment, twelve hydrophobic BPs accumulated in the TECAM with concentrations ranging from 251 ng g-1 to 6283 ng g-1, and three hydrophilic BPs did not accumulate during the 72 h exposure duration. BPs accumulations were determined by the hydrophilic and hydrophobic substituent groups in molecule structures. The estimated passive sampling parameters showed correlations to both the log Kow values and chemical structures, and compared to other contaminants, such as organophosphorus flame retardants. Environmental factors, including flow rate, temperature, salinity, and pH, that affect the accumulation of BPs in the TECAM were tested, and the flow rate was found to be an important factor affecting the uptake rate. The isotropic exchange kinetics for BPs in the TECAM were verified, and the results indicated that BPs can be calibrated with performance reference compounds (PRCs) in field applications. Finally, a field deployment of TECAM in river waters successfully estimated the time-weighted concentrations of two hydrophobic BPs. To address the inherent weaknesses of TECAM in sampling hydrophilic and moderately hydrophobic BPs, future studies should explore alternative passive samplers, such as hydrophilic-lipophilic balance sorbent-embedded cellulose acetate membranes, to sample BPs in surface waters.


Assuntos
Trioleína , Poluentes Químicos da Água , Celulose/análogos & derivados , Monitoramento Ambiental , Membranas Artificiais , Poluentes Químicos da Água/análise
3.
Environ Sci Pollut Res Int ; 25(21): 20823-20832, 2018 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-29761355

RESUMO

Hexabromocyclododecanes (HBCDs) are a class of widely used brominated flame retardants (BFRs) that exhibit strong hydrophobicity. The ubiquity and persistence of HBCDs in sediment have attracted significant attention because of public health concerns. The environmental fate and ecological risks of HBCDs closely depend on their phase distribution in sediments. However, little information is available regarding the freely dissolved concentrations (Cfree) of HBCDs in sediment porewater. In this study, we developed a method to measure Cfree of HBCDs in sediment porewater using triolein-embedded cellulose acetate membranes (TECAM). The TECAM-to-water partitioning coefficient (log KTECAM) was 4.69, 4.77, and 4.63 for α-HBCD, ß-HBCD, and γ-HBCD, respectively. In sediments, HBCDs sorbed to the sediment solid phase accounted for more than 99% of the total chemical mass. The dissolved organic carbon (DOC)-water partition coefficient (KDOC) values were derived from TECAM measurements, and the log KDOC values ranged from 5.77 to 6.23 for the three HBCD diastereomers, suggesting a strong tendency for HBCDs to sorb to DOC. The high sorption of HBDCs for DOC implies a potential for DOC-facilitated transport which may enhance the environmental mobility of HBCDs.


Assuntos
Celulose/análogos & derivados , Monitoramento Ambiental/métodos , Sedimentos Geológicos/química , Hidrocarbonetos Bromados/análise , Trioleína/química , Poluentes Químicos da Água/análise , Celulose/química , China , Retardadores de Chama , Hidrocarbonetos Bromados/química , Interações Hidrofóbicas e Hidrofílicas , Modelos Teóricos , Solubilidade , Estereoisomerismo , Água/química , Poluentes Químicos da Água/química
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