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Self-sacrificial biomass-derived silica is a rising and promising approach to fabricate large metal silicates, which are practical water treatment agents ascribed for easy sedimentation and separation. However, the original biomass architecture is difficult to be maintained and utilized. Furthermore, sufficient ion diffusion pathways need to be created to satisfy massive mass transport in large bulk materials. Herein, a series of metal silicates, including cobalt silicate (CoSiO), copper silicate, nickel silicate, iron silicate, and magnesium silicate, are synthesized from Indocalamus tessellatus leaf as the biomass-derived silica source and investigated as catalysts in sulfate-radical-based advanced oxidization processes (SR-AOPs) for the first time. Among them, CoSiO presents an analogical sandwich structure as a leaf-derived template of micron-level size. More importantly, the interior hollow nanotubes assembled by small nanosheets provide numerous pathways for ion diffusion and remarkably promote the mass transport in such large bulk materials. Owing to the combination of the unique structure with the high reactivity of Co (II) toward peroxymonosulfate, CoSiO exhibits excellent catalytic performance with 0.242 and 0.153 min rate constants for the removal of methylene blue and phenol, respectively, which outperforms/is comparable to that of the reported nanomaterials toward organic contaminants in SR-AOPs.
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http://dx.doi.org/10.1016/j.jcis.2019.03.017 | DOI Listing |
Environ Sci Technol
August 2025
College of Chemistry, Chemical Engineering & Environmental Science, Minnan Normal University, Zhangzhou 363000, China.
Polymetallic nodules' (PMNs) deep-sea mining poses risks to marine ecosystems, yet its effects on surface picophytoplankton remain unclear. This study assessed metal release from PMNs and its impact on picophytoplankton in the Clarion-Clipperton zone through laboratory and field incubation experiments. PMNs particles, particularly finer ones, released chromium, cobalt, nickel, and copper more rapidly under light exposure, high salinity, and algal secretion.
View Article and Find Full Text PDFNanotechnology
July 2025
Zhejiang University of Technology, Hangzhou chaowang road 18, Hangzhou, Zhejiang, 310014, CHINA.
Cobalt-based catalysts demonstrate significant activity in activating peroxymonosulfate (PMS) for the degradation of water pollutants. Nevertheless, their practical application remains constrained due to concerns regarding potential cobalt leaching, associated toxicity risks, and overall stability under operational conditions. A novel CoCa-SBA-600 catalyst was synthesized via a hydrothermal-assisted SBA-15 sacrificial templating strategy, where the zeolite simultaneously served as a silicate precursor and structural scaffold.
View Article and Find Full Text PDFWater Res
October 2025
Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, PR China. Electronic address:
Understanding and controlling the structure-activity relationship of single atom catalysts (SACs) is crucial for optimizing their catalytic performance. This study investigated the influence of montmorillonite (MT) as a support material on the microstructure of SACs, and how these influences modulate the catalytic performance and mechanism of peroxymonosulfate (PMS) activation. The enrichment effect within the MT interlayer space significantly enhanced the interaction between organic pollutant molecules, PMS, and active sites, thereby improving adsorption capacity and mass transfer efficiency.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Hubei Key Laboratory of Radiation Chemistry and Functional Materials, School of Nuclear Technology and Chemistry & Biology, Hubei University of Science and Technology, Xianning 437100, PR China. Electronic address:
The development of cost-effective, high-efficiency oxygen evolution reaction (OER) catalysts through precise compositional and structural design via guest doping engineering represents a significant research challenge. While cobalt silicate (CoSi) has emerged as a promising OER catalyst, its practical application has been limited by relatively high overpotential (η). In this study, we presented a strategic Fe-doping approach to engineer the electronic structure of CoSi, significantly enhancing its OER performance.
View Article and Find Full Text PDFJ Colloid Interface Sci
November 2025
Key Laboratory of Special Functional Materials for Ecological Environment and Information (Hebei University of Technology), Ministry of Education, Tianjin 300130, China; Institute of Power Source and Ecomaterials Science, Hebei University of Technology, Tianjin 300130, China. Electronic address: wan
The slow reaction rate of the oxygen evolution process (OER) and the high economic burden associated with precious metal catalysts significantly impede the practical adoption of OER-driven technologies. Despite recent advancements, the development of non-precious electrocatalysts with high OER activity and remarkable stability remains a significant scientific challenge. Herein, novel iron-doped cobalt silicate hydroxide (CoFeSi) electrocatalysts assembled with ultrathin nanosheets were successfully prepared using a facile hydrothermal method.
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