Understanding the transport behaviors of thallium (Tl) in porous media is of considerable interest for both natural soils and artificial filtration removal of Tl. In this context, the transport behaviors of Tl(I) in water-saturated sand columns under different conditions were systematically investigated. It was found that, in addition to the effects of pH and ionic strength (IS), the transport of Tl(I) depended on the carbonate, phosphate and macromolecular organic matter as well. Tl(I) broken the columns more difficultly under higher pH and lower IS conditions. Moreover, the adsorption of carbonate and phosphate on sand surfaces may increase the retention of Tl(I) in columns. As for macromolecular organic matter, humic acid (HA) facilitated Tl(I) transport, especially under neutral and alkaline conditions (7.0 and 9.8), which was possibly associated with Tl-complexes formation and competed adsorption between Tl(I) and HA. However, bovine serum albumin (BSA) impeded Tl(I) transport for the reason that deposited BSA might provide more adsorption sites for Tl(I), though Tl(I) had a slight effect on BSA transport. In order to evaluate the mechanisms of transport, a dual-sites non-equilibrium model was applied to fit the breakthrough curves of Tl(I). Retardation factor (R) values of individual Tl(I) transport from model calculations were found to be higher than that of Tl(I) transport with HA and lower than that of Tl(I) transport with BSA. The fraction of instantaneous sorption sites (β) was found to decrease with increasing pH, implying nonequilibrium sorption is a main sorption mechanism of Tl(I) with pH increasing. The fundamental data obtained herein demonstrated that carbonate, phosphate and macromolecular organic matter significantly influenced the Tl(I) migration and could lead to the leaking or bindings of Tl(I) at Tl-occurring sites.
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http://dx.doi.org/10.1016/j.watres.2020.116325 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
State Key Laboratory of Organic-Inorganic Composites, School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
With significantly high lithium-ion (Li) transport efficiency, single-ion conducting polymer electrolytes (SIPEs) often suffer from low ionic conductivity due to the covalently bonded anions to the polymer backbone. Adding plasticizers to SIPEs to improve ionic conductivity usually reduces the polymer matrix's mechanical robustness, negatively affecting overall performance as solid electrolytes. Herein, to surpass such a trade-off relationship, we successfully designed a single-ion conducting composite membrane (c-SIPM60) with cross-linked linear SIPEs and incorporated glass-mesh substrate, which shows a cation transport number close to 1, ultrahigh tensile strength of 22 MPa (modulus of 547.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Department of Physics, Nanchang University, Nanchang 330031, China. Electronic address:
Polyvinylidene fluoride (PVDF) materials have been widely investigated as polymer matrix for solid polymer electrolytes (SPEs) due to their high dielectric constant, electroactive effect (piezo-, pyro-, and ferroelectricity), and excellent thermal stability. However, the poor interface compatibility caused by highly reactive residual solvents and unsatisfactory ionic conductivity owing to sluggish Li transport kinetics are principal bottlenecks impeding the further development of PVDF-based electrolytes. Herein, we design a PVDF-based electrolytes with the assistance of hydrophilic-amorphous silica (HA-SiO).
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November 2024
Guangxi Key Laboratory of Automobile Components and Vehicle Technology, Guangxi University of Science & Technology, Liuzhou 545006, China.
Lithium-ion batteries have garnered significant attention owing to their exceptional energy density, extended lifespan, rapid charging capabilities, eco-friendly characteristics, and extensive application potential. These remarkable features establish them as a critical focus for advancing next-generation battery technologies. However, the commonly used organic liquid electrolytes in batteries are explosive, volatile, and possess specific toxic properties, resulting in persistent safety concerns that remain to be addressed.
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January 2025
Beijing Key Laboratory for Optical Materials and Photonic Devices, Department of Chemistry, Capital Normal University, Beijing 100048, China.
Crystalline porous metal-organic frameworks (MOFs) have attracted great interest, including in the field of solid-state electrolytes. Herein, we report a new type of solid-state electrolyte based on an MOF matrix and a Li ionic liquid. By covalently bonding the Li ionic liquid (MIMS·LiTFSI) on the stable UiO-67 framework, the obtained crystalline IL-MOF material exhibited high ion conductivities within a wide temperature range (30 °C 1.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Xinjiang Key Laboratory of High Value Green Utilization of Low-Rank Coal, School of Physics and Materials Science, Changji University, Changji, Xinjiang, 831100, China.
The low lithium-ion conductivity of polyethylene oxide (PEO)-based polymer electrolytes limits their application in solid-state lithium batteries and related fields. Here, ionic liquids (ILs) are injected into hollow silicon nanorods (HSNRs) to prepare a composite solid polymer electrolyte (CSPE) with aligned HSNRs containing ILs (F-ILs@HSNRs). Applying a magnetic field promoted uniform dispersion and orientation of F-ILs@HSNRs in CSPE.
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