Purification of As(V)-contaminated water through adsorption by FeO-based materials is a promising technology due to its low-cost and high efficiency. Dispersing the FeO phase on silica supports can improve both the adsorption rate and capacity due to the reduction in FeO particle sizes and the prevention of clumping of the FeO particles. However, the clusters in conventional silica materials largely impede the diffusion of As(V) to reach the FeO sites dispersed inside the clusters. Here, by applying a gelatin template strategy, the structure of silica materials was tailored by changing the gelatin-to-silica ratio (0, 0.6, 1.2 and 1.8) and hydrothermal temperature (60 °C, 100 °C and 140 °C). The silica cluster size could be reduced using either a low gelatin-to-silica ratio (0.6) or a low hydrothermal temperature (60 °C). Increasing the gelatin-to-silica ratio to 1.2 created porous silica spheres with a hollow structure. The FeO-loaded hollow porous silica spheres with a shell thickness of 280 nm had twice the maximum As(V) adsorption capacity (7.66 mg g) compared to the FeO-loaded silica product prepared in the absence of gelatin (3.82 mg g). The maximum As(V) adsorption capacity could be further enhanced to 9.94 mg g by reducing the shell thickness to 80 nm through increasing the gelatin-to-silica ratio to 1.8 and the hydrothermal temperature to 140 °C. In addition, the best FeO-loaded hollow porous silica spheres had rapid As(V) adsorption and showed excellent durability as the As(V) removal efficiency slightly decreased to 98.9% subsequent to five adsorption-regeneration cycles.
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http://dx.doi.org/10.1016/j.chemosphere.2022.136356 | DOI Listing |
Langmuir
January 2025
Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112-0850, United States.
Modification of silica interfaces by covalent attachment of functional ligands is a primary means of controlling the interfacial chemistry of porous silicas used in separations, environmental cleanup, and biosensing. Recently, modification of hydrophobic, -alkyl-silane-functionalized interfaces has been achieved through self-assembly of zwitterionic phospholipids or mixed-charged surfactants to form "hybrid bilayers", producing interfaces that mimic lipid-bilayer partitioning and provide shape-selective partitioning of aromatic hydrocarbons. Charged headgroups, however, introduce electrostatic interactions that strongly influence the retention of ionizable solutes and require careful control over pH and ionic strength in the solution phase.
View Article and Find Full Text PDFAnal Chim Acta
February 2025
Key Laboratory of Molecular Medicine and Biotherapy, School of Life Science, Beijing Institute of Technology, No. 5 Zhongguancun South Street, Beijing, 100081, China. Electronic address:
Background: The metal organic cages (MOCs) are an emerging type of porous material that has attracted considerable research interest due to their unique properties, including good stability and well-defined intrinsic cavities. The chiral MOCs with porous structures have broad application prospects in enantiomeric recognition and separation. However, there are almost no relevant reports on chiral MOCs as chiral stationary phases (CSPs) for enantioseparation by high-performance liquid chromatography (HPLC).
View Article and Find Full Text PDFMaterials (Basel)
December 2024
Department of Architecture, Faculty of Science and Technology, Tokyo University of Science, Noda City 278-8510, Japan.
A fundamental study has been conducted on the effective utilization of rice husk ash (RHA) in concrete. RHA is an agricultural byproduct characterized by silicon dioxide as its main component, with a content of 90% or more and a porous structure that absorbs water during mixing, thereby reducing fluidity. The quality of RHA varies depending on the calcination environment; however, the effect is not consistent.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Organic-inorganic hybrid materials are explored for application as solid electrolytes for lithium-ion batteries. The material consists of a porous silica network, of which the pores are infiltrated by poly(ethylene oxide) and lithium perchlorate. The synthesis involves two steps: First, the inorganic backbone is created by the acid-catalyzed sol-gel synthesis of tetraethyl orthosilicate to ensure continuity of the backbone in three dimensions.
View Article and Find Full Text PDFMikrochim Acta
January 2025
School of Material Science and Engineering, Henan University of Technology Zhengzhou, Henan, 450001, China.
A simple, fast, and cost-effective colorimetric nitrite (NO) sensor based on ZIF-67-derived CoO nanocomposite (ZCo-2 NC) structure has been developed. The prepared colorimetric sensor (ZCo-2 NC) was employed to sensitively detect NO in drinking water system by the exhibition of promising peroxidase-mimicking nanozyme-like features. The sensor manifest well-determined sensing response with excellent linear and wide range of NO sensitivity (0.
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