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This study introduces an innovative and cost-effective biomass adsorbent, the sulfur/cardanol/potato starch composite (SCP), synthesized through inverse vulcanization for the remediation of mercury-contaminated waters. The SCP was characterized using Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM/EDS), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis (TGA) and X-ray Diffraction (XRD) to confirm its composition, morphology, and properties. The adsorption capacity of SCP for Hg(II) was 246.88 mg/g with a removal rate of 98.75 %. Adsorption kinetics followed a pseudo-second-order model, indicating chemisorption as the dominant mechanism, while adsorption isotherms were best described by the Langmuir model. Thermodynamic studies confirmed the adsorption process as spontaneous and endothermic. Density Functional Theory (DFT) calculations further elucidate the interaction mechanisms between mercury and the adsorbent, revealing that the thiyl radicals play a crucial role in the adsorption process. The SCP also exhibited a high selectivity for Hg(II) over other co-existing ions and maintains an adsorption capacity over 223.93 mg/g after five regeneration cycles, thus promising practical applications in environmental mercury management.
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http://dx.doi.org/10.1016/j.ijbiomac.2024.135868 | DOI Listing |
Environ Sci Technol
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China.
Pd-zeolites are promising passive NO adsorber (PNA) materials for mitigating cold-start emissions from lean-burn engines. However, their practical deployment is constrained by insufficient densities and dispersion of isolated Pd active sites as well as their susceptibility to hydrothermal degradation and phosphorus poisoning encountered in vehicle exhaust environments. Herein, we develop a rationally engineered core-shell Pd/SSZ-13@AlO composite, featuring a Pd/SSZ-13 core encapsulated within a mesoporous AlO shell.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University, Changzhou 213164, P. R. China.
The development of high-performance, cost-effective non-noble metal catalysts for the oxygen evolution reaction (OER) is critical to advancing sustainable hydrogen production via water electrolysis. Herein, we report a facile and mild strategy for synthesizing amorphous bimetallic organic framework materials (NiFe-MOFs) using pyridine-modified threonine (l-PyThr) as an organic ligand. The optimized NiFe-PyThr-4:1 catalyst exhibits remarkable OER activity, requiring low overpotentials of only 162 and 222 mV to achieve current densities of 10 and 100 mA cm, respectively, along with a small Tafel slope of 34.
View Article and Find Full Text PDFJ Vis Exp
August 2025
Tencent Quantum Laboratory;
Electrolytes are important components in lithium-ion batteries. However, battery degradation due to irreversible electrochemical reactions in the electrolyte can consume electrolyte molecules and severely reduce its effective operation lifetime. It is hence important to study the electrochemical reaction pathways in the battery electrolyte to further improve lithium-ion battery reliability.
View Article and Find Full Text PDFACS Nano
September 2025
School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China.
Chemical C-N coupling from CO and N toward urea synthesis is an appealing approach for Bosch-Meiser urea production. However, this process faces significant challenges, including the difficulty of N activation, high energy barriers, and low selectivity. In this study, we theoretically designed a Ni triple-atom doped CuO catalyst, Ni TAC@CuO, which exhibits exceptional urea synthesis performance.
View Article and Find Full Text PDFLangmuir
September 2025
College of Applied Science and Technology, Hainan University, Haikou 570228, China.
This study systematically investigates the role of nitrogen annealing in enhancing the structural and electrochemical properties of ZnNiO/NF composite anode materials synthesized via hydrothermal methods. By comparing air-annealed and nitrogen-annealed (400 and 600 °C) samples, it is demonstrated that nitrogen annealing at 400 °C induces the densely stacked nanosheet morphology with optimized lattice regularity, which can significantly improve the charge transport kinetics and the interfacial stability. Electrochemical evaluations reveal an outstanding initial discharge capacity of 1873.
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