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The use of construction waste red brick powder (RBP) to prepare adsorbents for phosphate removal from wastewater represents a promising technology with substantial research potential. This study investigates the preparation of La-based magnetic red brick powder (La-Fe-RBP) via bimetallic modification to enhance its adsorption performance. The key characteristics, adsorption process, adsorption mechanism, and practical applications of the modified adsorbent were analyzed. The obtained results suggested that the underlying adsorption mechanism of La-Fe-RBP was best described by the Langmuir and pseudo-second-order kinetic models, which suggested that the adsorption mechanism was monolayer chemical adsorption. La-Fe-RBP exhibited rapid kinetics, achieving adsorption saturation in just 40 min, significantly faster than RBP (360 min). Additionally, isotherm experiments determined the highest theoretical adsorption capacity as 42.835 mg/g. More importantly, La-Fe-RBP exhibited efficient phosphate adsorption within a pH ranging from 3 to 8. Furthermore, La-Fe-RBP exhibited high selectivity for phosphate ions in the presence of coexisting ions (SO42-, NO3-, Cl, HCO3-, Mg, and Ca), demonstrating its robustness and effectiveness in complex water conditions. FTIR and XPS analyses demonstrated that ligand exchange and electrostatic attraction were the primary mechanisms underlying phosphate adsorption by La-Fe-RBP. Domestic sewage treated with La-Fe-RBP met the Class IV surface water environmental quality standards in China. The findings of this study prove that the La-Fe-RBP composite material, characterized by high adsorption efficiency and strong selectivity, holds significant potential for removing phosphates from real wastewater.
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http://dx.doi.org/10.3390/ma18061326 | DOI Listing |
Mikrochim Acta
September 2025
Department of Public Health Laboratory Sciences, College of Public Health, Hengyang Medical School, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, China.
We systematically evaluated the DNA adsorption and desorption efficiencies of several nanoparticles. Among them, titanium dioxide (TiO₂) nanoparticles (NPs), aluminum oxide (Al₂O₃) NPs, and zinc oxide (ZnO) NPs exhibited strong DNA-binding capacities under mild conditions. However, phosphate-mediated DNA displacement efficiencies varied considerably, with only TiO₂ NPs showing consistently superior performance.
View Article and Find Full Text PDFAdv Mater
September 2025
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, State Key Laboratory of Organic-Inorganic Composites, Bionanomaterials & Translational Engineering Laboratory, Beijing Key Laboratory of Bioprocess, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical
Sonocatalytic therapy (SCT) is a non-invasive tumor treatment modality that utilizes ultrasound (US)- activated sonocatalysts to generate reactive oxygen species (ROS), whose production critically dependent on the electronic structural properties of the catalytic sites. However, the spin state, which is a pivotal descriptor of electronic properties, remains underappreciated in SCT. Herein, a Ti-doped zirconium-based MOF (Ti-UiO-66, denoted as UTN) with ligand-deficient defects is constructed for SCT, revealing the important role of the electronic spin state in modulating intrinsic catalytic activity.
View Article and Find Full Text PDFLangmuir
September 2025
School of Resources and Safety Engineering, Chongqing University, Chongqing 400044, China.
Hydrogen energy is pivotal for driving sustainable development and achieving deep decarbonization; yet, its storage remains a significant challenge. Notably, depleted methane reservoirs can serve as a promising large-scale solution for underground hydrogen storage (UHS). Based on adsorption experiments, Monte Carlo and molecular dynamics methods, the adsorption behavior of H and CH in anthracite and the applicability of five models were discussed.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Electrochemical synthesis of ammonia (NH) is a promising green alternative to the conventional Haber-Bosch process. Here, we report the synthesis of a heteroatomic metal-metal bonded dual atomic (DA) Mn-Cu catalytic site embedded within nitrogen-doped carbon (NC) matrix for high-performance electrochemical reduction of N to NH. The asymmetric electronic distribution localized at the dual atomic sites synergistically enhances the adsorption and activation of N, facilitating the complex proton-coupled electron transfer process.
View Article and Find Full Text PDFInorg Chem
September 2025
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, PR China.
Confronting the dual challenges of carbon neutrality and sustainable energy, photocatalytic CO reduction requires precise control over product selectivity. This study demonstrates that surface hydroxyl (-OH) density serves as a molecular switch for reaction pathways in graphene oxide/cobalt tetraphenylporphyrin (GO/CoTPP) hybrids. By tuning the reduction degree of GO supports via gradient hydrazine hydrate treatment (0-85%), we constructed catalysts with controlled -OH concentrations.
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