The rational design of novel adsorption materials is imperative to remove toxic metal species from the polluted water. Herein, a core@shell structural Fe-FeO@poly (hexachlorocyclotriphosphazene-co-polyethylenimine) (Fe-FeO@PHCP) magnetic nanochain with high saturation magnetization was fabricated and used for effective adsorption and reduction of hexavalent chromium. The morphology and microstructure of Fe-FeO@PHCP were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The effects of concentration, pH, contact time, temperature and coexisting ions on Cr (VI) removal were studied. Four kinetic models (pseudo-first-order, pseudo-second-order, Bangham and intraparticle diffusion models) and two isotherm models (Freundlich and Langmuir) were used to fit experimental data. Results show the adsorption capacity of Fe-FeO@PHCP for Cr (VI) is up to 229.0 mg g. The excellent performance was ascribed to the favorable reduction of Cr (VI) to Cr (III), followed by the chelation of Cr (III) with imino groups. Meanwhile, the residual Cr (VI) were adsorbed on protonated amino and imino groups. The adsorption process is exothermic and spontaneous and nicely follows pseudo-second-order kinetics, intraparticle diffusion model and Langmuir isotherm model. These results indicated that easily separable Fe-FeO@PHCP magnetic nanochains could be a promising adsorbent to remediate chromate wastewater.
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http://dx.doi.org/10.1016/j.jhazmat.2019.121483 | DOI Listing |
J Phys Chem Lett
January 2025
Key Laboratory of Physics and Technology for Advanced Batteries, Ministry of Education, College of Physics, Jilin University, Qianjin Street No. 2699, Changchun 130012, China.
Developing heavy-metal-free materials with wide tunable emission is important to light-emitters. The alloying method is utilized in ZnSe magic size clusters (MSCs) with Te to form ZnSeTe and manipulate the band gap structure in ZnSe. The growth of ZnTe on alloyed ZnSeTe quantum dots (QDs) forms ZnSeTe/ZnTe core/shell nanostructures, showing the tunable photoluminescence emission peak from 450 to 760 nm with the different thicknesses of ZnTe shell.
View Article and Find Full Text PDFACS Chem Neurosci
January 2025
Unconventional Computing Laboratory, University of the West of England, Bristol BS16 1QY, U.K.
This study examines the effects of incorporating serotonin (5-HT) into proteinoid microspheres. It looks at the microspheres' structure and electrochemical properties. Proteinoid-serotonin assemblies have better symmetry and membrane organization than pristine proteinoids.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Department of Cardiology, The First People's Hospital of Wenling, Wenling Hospital of Wenzhou Medical University, Wenling, Zhejiang, 317500, China.
Immobilizing enzymes onto solid supports having enhanced catalytic activity and resistance to harsh external conditions is considered as a promising and critical method of broadening enzymatic applications in biosensing, biocatalysis, and biomedical devices; however, it is considerably hampered by limited strategies. Here, a core-shell strategy involving a soft-core hexahistidine metal assembly (HmA) is innovatively developed and characterized with encapsulated enzymes (catalase (CAT), horseradish peroxidase, glucose oxidase (GOx), and cascade enzymes (CAT+GOx)) and hard porous shells (zeolitic imidazolate framework (ZIF), ZIF-8, ZIF-67, ZIF-90, calcium carbonate, and hydroxyapatite). The enzyme-friendly environment provided by the embedded HmA proves beneficial for enhanced catalytic activity, which is particularly effective in preserving fragile enzymes that will have been deactivated without the HmA core during the mineralization of porous shells.
View Article and Find Full Text PDFSmall
January 2025
Institute of Translational Medicine, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, China.
In this study, we present an ultrasensitive and specific multiplexed detection method for SARS-CoV-2 and influenza (Flu) utilizing CRISPR/Cas13a technology combined with a hydrogel-encapsulated photonic crystal (PhC) barcode integrated with hybridization chain reaction (HCR). The barcodes, characterized by core-shell structures, are fabricated through partial replication of periodically ordered hexagonally close-packed silicon dioxide beads. Consequently, the opal hydrogel shell of these barcodes features abundant interconnected pores that provide a substantial surface area for probe immobilization.
View Article and Find Full Text PDFJ Mol Model
January 2025
Institute of Molecular Science, Shanxi University, Taiyuan, 030006, China.
Context: Inspired by the newly synthesized endohedral fullerene T CH@C (1) and based on extensive density functional theory calculations, we predict herein a series of endohedral borafullerenes C CH@BC (4), T BH@BC (5), C HO@BC (6), C NH@BC (7), and T C@BC (8) which possess a BC (3) shell isovalent with C, with the neutral D C@BC (9) obtained from C@BC (8) by symmetric C─B substitutions. Detailed adaptive natural density partitioning (AdNDP) bonding analyses and iso-chemical shielding surfaces (ICSSs) calculations indicate that these core-shell species are spherically aromatic in nature, rendering high stability to the systems. More interestingly, based on the calculated effective donor-acceptor interaction between LP(O) → LV(B@BC) in HO@BC (6), we propose the concept of boron bond (BB) in chemistry which is defined as the in-phase orbital overlap between an electronegative atom A as lone-pair (LP) donor and an electron-deficient boron atom with a lone vacant (LV) orbital as LP acceptor.
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