Journal
SCIENCE OF THE TOTAL ENVIRONMENT
Volume 627, Issue -, Pages 905-915Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.scitotenv.2018.01.273
Keywords
Laboratory calibration; Polar organic chemical integrative sampler (POCIS); Mixed polymer sampler (MPS); Sampling rate (R-S); Sampler-water partition coefficient (K-SW); Membrane sorption
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Funding
- internal project of KIST Europe [11796]
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In this work, Oasis HLB (R) beads were embedded in a silicone matrix to make a single phase passive sampler with a higher affinity for polar and ionisable compounds than silicone alone. The applicability of this mixed polymer sampler (MPS) was investigated for 34 aquatic contaminants (log K-OW -0.03 to 6.26) in batch experiments. The influence of flow was investigated by comparing uptake under static and stirred conditions. The sampler characteristics of the MPS was assessed in terms of sampling rates (R-S) and sampler-water partition coefficients (K-SW), and these were compared to those of the polar organic chemical integrative sampler (POCIS) as a reference kinetic passive sampler. The MPS was characterized as an equilibrium sampler for both polar and non-polar compounds, with faster uptake rates and a shorter time to reach equilibrium than the POCIS. Water flow rate impacted sampling rates by up to a factor of 12 when comparing static and stirred conditions. In addition, the relative accumulation of compounds in the polyethersulfone (PES) membranes versus the inner Oasis HLB sorbent was compared for the POCIS, and ranged from <1% to 83% depending on the analyte properties. This is indicative of a potentially significant lag-phase for less polar compounds within POCIS. The findings of this study can be used to quantitatively describe the partitioning and kinetic behaviour of MPS and POCIS for a range of aquatic organic contaminants for application in field sampling. (C) 2018 Elsevier B.V. All rights reserved.
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