Polar organic chemical integrative sampler (POCIS) contains sorbent, which is typically enclosed between two polyethersulfones (PES) membranes. A significant PES uptake is reported for many contaminants, yet, aqueous concentration is mainly correlated with the sorbent uptake using first-order kinetics. Under high PES sorption, the first-order kinetics often provide erroneous sampling rate for the sorbent phase due to increased membrane resistance. This work evaluated the uptake of four high PES sorbing chemicals, i.e., three Cl- and CH-substituted nitrobenzenes and one chlorinated aniline using POCIS and the potential of a single-phase PES sampler using laboratory experiments. POCIS calibration results demonstrated that both sorbent and membrane had similar affinity for the target compounds. A rapid PES sorption occurred in the earlier days (<7 days) followed by a gradual increase in the PES phase concentration (equilibrium not achieved after 60 days). Especially, the membrane was the primary sink for 3,4-dichloroaniline and 3,4-dichloronitrobenzene for up to 14 and 31 days, respectively. On the other hand, the single-phase PES sampler showed similar mass uptake as POCIS and reached equilibrium within 19 days under static condition, indicating its potential suitability in the equilibrium regime. PES-water partition coefficient of the target compounds was between 1.2 and 6.5 L/g. Finally, we present a poly-parameter linear-free energy relationship (pp-LFER) using published data to predict the PES-water partition coefficients. The pp-LFER models showed moderate predictability as indicated by R values between 0.7 and 0.9 for both internal and external data set consisting of a wide range of hydrophobic and hydrophilic compounds (-0.1 ≤ logK ≤ 7.4). The proposed pp-LFER model can be used to screen high PES-sorbing chemicals to increase the reliability and accuracy of aqueous concentration prediction from POCIS sampling and to select the most appropriate sampling approach for new compounds.
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http://dx.doi.org/10.1016/j.scitotenv.2022.157898 | DOI Listing |
Nat Commun
December 2024
Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Spin-polarized lasers have demonstrated many superiorities over conventional lasers in both performance and functionalities. Hybrid organic-inorganic perovskites are emerging spintronic materials with great potential for advancing spin-polarized laser technology. However, the rapid carrier spin relaxation process in hybrid perovskites presents a major bottleneck for spin-polarized lasing.
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December 2024
Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China.
Piezoelectric electronics possess great potential in flexible sensing and energy harvesting applications. However, they suffer from low electromechanical performance in all-organic piezoelectric systems due to the disordered and weakly-polarized interfaces. Here, we demonstrated an all-polymer piezo-ionic-electric electronics with PVDF/Nafion/PVDF (polyvinylidene difluoride) sandwich structure and regularized ion-electron interfaces.
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December 2024
Beijing Key Laboratory for Membrane Materials and Engineering, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Two-dimensional (2D) metal-organic framework (MOF) nanosheet membranes hold promise for exact molecular transfer due to their structural diversity and well-defined in-plane nanochannels. However, achieving precise regulation of stacking modes between neighboring nanosheets in membrane applications and understanding its influence on separation performance remains unrevealed and challenging. Here, we propose a strategy for accurately controlling the stacking modes of MOF nanosheets via linker polarity regulation.
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December 2024
State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Collaborative Innovation Center for Guangxi Ethnic Medicine, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, 541004, PR China. Electronic address:
Sensitive and accurate determination of tumour biomarkers is extremely important for early cancer diagnosis. Herein, a photoelectrochemical biosensor platform was constructed for ultrasensitive tumour biomarker detection by utilizing Au@CuO to switch the photocurrent polarity of CdS/Ni-catecholates metal-organic framework (Ni-CAT) nanorod arrays grown in situ on ITO. The Ni-CAT obtains close contact with ITO and forms a Z-scheme heterojunction with CdS, which improves the photogenerated electron transfer ability.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
December 2024
Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Flemingovo náměstí 2, 16610, Prague, Czech Republic; Department of Analytical Chemistry, University of Chemistry and Technology, Technická 5, 16628 Prague, Czech Republic. Electronic address:
Water is a greatly convenient solvent in Raman spectroscopy. However, non-additive effects sometimes make its signal difficult to subtract. To understand these effects, spectra for clusters of model ions, including transition metal complexes and water molecules, were simulated and analyzed.
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