An adsorptive stripping voltammetric procedure for the determination of U(VI) at an in situ plated lead film electrode is described. The U(VI) complex with cupferron was accumulated from an acetate buffer solution of pH 4.2 at the potential -0.65V. The measurements were carried out from undeaerated solutions. The calibration graph for an accumulation time of 180s was linear from 5x10(-10) to 2x10(-8)molL(-1). The detection limit was 2x10(-10)molL(-1), the relative standard deviation for 2x10(-8)molL(-1) U(VI) was 4.3%. The proposed procedure was validated in the course of U(VI) determination in water certified reference materials.
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http://dx.doi.org/10.1016/j.talanta.2006.12.026 | DOI Listing |
Anal Chim Acta
February 2025
Chemistry Department, Faculty of Science, Ain-Shams University, Cairo, 11566, Egypt; Department of Chemistry, Faculty of Science, Galala University, New Galala City, Suez, Egypt. Electronic address:
Background: Electrochemical methods, particularly those utilizing sensors, offer distinct advantages over classical analytical methods. They are cost-effective, compatible with mass fabrication, suitable for remote sensing, and can be designed as handheld analyzers. In this context, MIL-101(Cr)-(COOH)₂@MWCNTs was utilized for the first time as a modifier for GCE for the sensitive voltammetric detection of Pb(II), Cu(II), and Hg(II).
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Chemistry, University College London, London, WC1E 7JE, UK.
Long-standing challenges including notorious side reactions at the Zn anode, low Zn anode utilization, and rapid cathode degradation at low current densities hinder the advancement of aqueous zinc-ion batteries (AZIBs). Inspired by the critical role of capping agents in nanomaterials synthesis and bulk crystal growth, a series of capping agents are employed to demonstrate their applicability in AZIBs. Here, it is shown that the preferential adsorption of capping agents on different Zn crystal planes, coordination between capping agents and Zn ions, and interactions with metal oxide cathodes enable preferred Zn (002) deposition, water-deficient Zn ion solvation structure, and a dynamic cathode-electrolyte interface.
View Article and Find Full Text PDFSmall Methods
January 2025
Hunan Provincial Key Laboratory of Chemical Power Sources, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, P. R. China.
Anode-less sodium metal batteries (SMBs) suffer from the formation of Na dendrites and inactive Na on an anode substrate though showing advantages of high energy densities and low costs. Herein, N,O co-doped carbon spheres (NOCS), which are synthesized via a scalable polymerization and pyrolysis method, are employed as a thin and stable sodiophillic nucleation layer on the Cu foil. Combined with electrochemical measurements, Na deposition morphology observations and density functional theory calculations, it is revealed that the introduced N and O heteroatoms can greatly enhance the adsorption of Na on the carbon substrate and reduce the nucleation overpotential, thus forming sufficient seeding sites and guiding homogeneous Na deposition.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, China.
Porous organic polymers have shown great potential in photocatalytic CO reduction due to their unique tunable structure favoring gas adsorption and metal sites integration. However, efficient photocatalysis in porous polymers is greatly limited by the low surface reactivity and electron mobility of bulk structure. Herein, we incorporate TiO nanoparticles and Ni(II) sites into a layered cationic imidazolium polymer (IP), in which the imidazolium moieties and free anions can stabilize the key intermediates and enhance the reaction kinetics of CO reduction.
View Article and Find Full Text PDFMikrochim Acta
December 2024
Chemistry Department, Faculty of Science, Tanta University, Tanta, Egypt.
The detection of 4-chloro-2-methylphenoxyacetic acid (CMPA) herbicide is crucial due to the potential health risks linked to exposure through drinking water, air, and food, which may adversely affect liver and kidney functions. To address this environmental concern and promote sustainable agriculture, a sensitive carbon paste sensor incorporating a composite material was developed. The composite sensor is based on porous cobalt-1,4-benzenedicarboxylate metal-organic framework and exfoliated montmorillonite nanolayers (Co-OF/MMt).
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