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The evaluation of the ecotoxicological risk of nickel (Ni) in surface water is hampered by a lack of speciation data. Six surface waters were sampled and speciation of Ni(II) was measured by the Donnan membrane technique (DMT) combined with radiochemical determination of 63Ni. The free Ni2+ ion fraction in the dissolved (<0.45 microm) phase was determined at background Ni concentration ((4-8) x 10(-8) M) and at concentrations in the range of toxicity thresholds for the Ni sensitive species Cerodaphnia dubia (5 x 10(-8) to 2 x 10(-6) M). The free ion fraction ranged from 4 to 45% at background Ni and increased with increasing Ni concentration and water hardness and with decreasing pH. The equilibration time after addition of Ni2+ (3h-7d) did not significantly change the measured free ion fraction. Predictions of the Humic-Ion Binding Model WHAM (Windermere Humic Aqueous Model) VI overestimated the observed free Ni2+ fraction (median>two-fold), even when assuming that all dissolved organic matter (DOM) was present as fulvic acid (FA). The impact of several model parameters affecting the prediction of Ni speciation were evaluated, including the solubility product of Fe(OH)3, which affects the Fe competition for complexation by DOM. The best fit (R2=0.88) was obtained by increasing only the distribution term DeltaLK2, which modifies the binding strength of multi-dentate sites, to accommodate the observed dependence of free ion fraction on Ni concentration.
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http://dx.doi.org/10.1016/j.aca.2006.06.070 | DOI Listing |
J Colloid Interface Sci
September 2025
Hebei Provincial Key Laboratory of Green Chemical Technology and High Efficient Energy Saving, Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China. Electronic address:
Enhancing anodic hydroxyl (OH) coverage and suppressing leaching of active metal sites are essential for developing efficient and durable alkaline oxygen evolution reaction (OER) electrocatalysts. Herein, we propose amorphous cerium oxide (CeO)-mediated amorphous/crystalline heterointerface engineering to enhance OH coverage and leaching resistance in CeO/Mo-NiS for high-performance OER. CeO with an oxyphilic surface facilitates OH adsorption, promoting in situ reconstruction of NiS into nickel hydroxyl oxide (NiOOH) with significantly enhanced OH coverage and thereby accelerating OER kinetics.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Cross-electrophile coupling (XEC) reactions are considered to be among the most fundamental construction of carbon-carbon bonds in organic chemistry. Traditionally, stoichiometric reductants, including metallic and organic reagents, are required to promote these conversions, resulting in significant waste that contributes to environmental pollution and increased disposal costs. In this study, we report a divided electrochemical synthesis-based cross-coupling platform in which HO is oxidized at the anode surface to generate electrons that produce a lower oxidation state nickel catalyst on the cathode surface, enabling XEC reactions without the need for metallic or organic reagents.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, and College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
The enantioselective construction of quaternary carbon stereocenters bearing amine functionalities represents a significant challenge in organic synthesis despite their prevalence in pharmaceutically active compounds. Herein, we report a versatile metallaphotoredox platform for the asymmetric incorporation of amine fragments onto quaternary carbons via coupling of alkene-tethered aryl bromides with readily available α-silylamines. This transformation proceeds under mild conditions without requiring organometallic reagents or stoichiometric reductants.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, PR China; Zhejiang Sci-Tech University Shengzhou Innovation Research Institute, Shengzhou 312400, PR China. Electronic address:
Suppressing photoinduced charge recombination represents a critical challenge in photocatalytic ammonia (NH) decomposition for hydrogen (H) production. Herein, we propose a dual-cocatalyst system comprising plasmonic silver (Ag) and nickel oxide (NiO), which synergistically construct an Ag → titanium dioxide (TiO) → NiO directional electron cascade on TiO surfaces through work-function-induced interfacial charge transfer. The optimized 3 %Ag-1 %NiO-TiO reaches a significantly photocatalytic H production rate of 2366.
View Article and Find Full Text PDFJASA Express Lett
September 2025
IEMN (UMR CNRS 8520), University Polytechnique Hauts-de-France, CNRS, University Lille, INSA HdF, F-59313 Valenciennes,
This study presents a non-destructive method for estimating surface acoustic wave attenuation, which is highly sensitive to microstructural features, especially at high frequencies. The method uses a single wideband dispersive interdigital transducer (IDT) that remotely emits acoustic waves at the sample's edge. Chirp compression of the temporal displacement response is achieved by correlating the excitation signal with the spatial configuration of the IDT's electrodes.
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