Coal-based humic acid residue (HAS), as a waste generated during humic acid production, has been gaining attention in recent years due to its adsorption capacity and containing nutrients. In this study, to improve the adsorption capacity of HAS for and Hg, phosphate-modified materials (N-HAS) were prepared by a hydrothermal method and HAS and N-HAS were characterized by scanning electron microscopy (SEM), Fourier transforms infrared spectroscopy (FTIR), X-ray fluorescence (XRF); batch adsorption experiments investigated the adsorption capacity of N-HAS on Hg under different pH, and isothermal adsorption model and kinetic model fitted the adsorption process to explore the adsorption mechanism; the effects of various amounts of N-HAS on the Hg content in maize and the effective Hg in the soil under Hg-contaminated soil were investigated by field trial. The results showed that the pseudo-second-order kinetic model (R=0.9641) and Langmuir isothermal (R=0.95) adsorption model could better describe the adsorption behavior of N-HAR on Hg, the maximum adsorption amount was 124.20 mg/g, and the time to reach adsorption equilibrium was shorter for N-HAS compared to HAS; after 5 times of adsorption-desorption, the removal rate of Hg by N-HAS was still higher than 80%, with stable cyclic adsorption performance; the adsorption mechanism of Hg by N-HAS included physical adsorption, precipitation, and surface complexation, and compared with HAS, the percentage of complexation for Hg adsorption by N-HAS increased by 77.81%, and the percentage of precipitation increased by 7.68%; compared to the control group, it was shown that the addition of N-HAS significantly decreased (p < 0.05) the Hg content of maize kernels by 27.44% ∼ 72.09%, increased biomass by 4.34% ∼ 11.26%, and decreased the available Hg content in soil by 50.00% ∼ 82.80%. In addition, the addition of N-HAS at 0.4 kg/m was optimal for the field trial. The study showed that N-HAS not only achieved resource utilization but also demonstrated great potential for treating Hg in water and soil.
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http://dx.doi.org/10.1016/j.envpol.2025.125657 | DOI Listing |
ACS Nano
January 2025
Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.
Transition-metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS), have emerged as a generation of nonprecious catalysts for the hydrogen evolution reaction (HER), largely due to their theoretical hydrogen adsorption energy close to that of platinum. However, efforts to activate the basal planes of TMDs have primarily centered around strategies such as introducing numerous atomic vacancies, creating vacancy-heteroatom complexes, or applying significant strain, especially for acidic media. These approaches, while potentially effective, present substantial challenges in practical large-scale deployment.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Energy Engineering, Hanyang University, Seoul 04763, Republic of Korea.
Lithium-tellurium (Li-Te) batteries are gaining attention as a promising next-generation energy storage system due to their superior electrical conductivity and high volumetric capacity compared to sulfur and selenium. Tellurium's unique properties, such as suitable redox potential, excellent conductivity, high volumetric capacity, and greatest stability, position it as a strong candidate for negative electrode materials. This study explores the potential of metal tellurides, specifically CuTe and FeTe monolayers, as effective tellurium host materials, leveraging their polar interactions with lithium polytellurides.
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January 2025
State Key Laboratory of Fine Chemicals, Research and Development Center of Membrane Science and Technology, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China.
The electrocatalytic nitrogen reduction reaction (eNRR) is an attractive strategy for the green and distributed production of ammonia (NH); however, it suffers from weak N adsorption and a high energy barrier of hydrogenation. Atomically dispersed metal dual-site catalysts with an optimized electronic structure and exceptional catalytic activity are expected to be competent for knotty hydrogenation reactions including the eNRR. Inspired by the bimetallic FeMo cofactor in biological nitrogenase, herein, an atomically dispersed FeMo dual site anchored in nitrogen-doped carbon is proposed to induce a favorable electronic structure and binding energy.
View Article and Find Full Text PDFAdv Mater
January 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225009, P. R. China.
Biomimetic calcification is a micro-crystallization process that mimics the natural biomineralization process, where biomacromolecules regulate the formation of inorganic minerals. In this study, it is presented that a protein-assisted biomimetic calcification method for the in situ synthesis of nitrogen-doped metal-organic framework (MOF) materials. A series of unique core-shell structures are created by utilizing proteins as templates and guiding agents in the nucleation step, creating ideal conditions for shell growth.
View Article and Find Full Text PDFAdv Mater
January 2025
State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, China.
Copper-based electrocatalysts are recognized as crucial catalysts for CO electroreduction into multi-carbon products. However, achieving copper-based electrocatalysts with adjustable valences via one-step facile synthesis remains a challenge. In this study, Cu/CuO heterostructure is constructed by adjusting the anion species of the Cu ions-containing electrolyte during electrodeposition synthesis.
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