Aluminum hydroxide is an effective defluoridation adsorbent; however, the poor defluoridation performance limits its wide application. In this work, amorphous and crystalline AlOOH adsorbents are synthesized through hydrolysis of Al salts, and their defluoridation performances are evaluated in terms of adsorption capacity and rate, sensitivity to pH value, and water quality after defluoridation. The defluoridation performance of AlOOH is closely related to the hydrolysis pH value, but hardly to the type of Al salts. The adsorbent can remove >95% fluoride in the first 2 min and reach adsorption equilibrium within 2 h, and the maximum defluoridation capacity is 41.9 mg/g. Furthermore, the adsorbent exhibits an excellent defluoridation efficiency at a wide pH range of 4.5-10.5. After fluoride removal, the adsorbents prepared at pH values of 6 and 7 exhibit low residual Al concentration. The Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) results confirm that the fluoride removal mechanism is the ligand exchange between fluoride and hydroxyl groups. The excellent defluoridation capacity and low residual Al demonstrate that AlOOH is a potential adsorbent for fluoride separation from water.
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http://dx.doi.org/10.1021/acsomega.1c01620 | DOI Listing |
Chem Sci
January 2025
Yusuf Hamied Department of Chemistry, University of Cambridge Lensfield Road Cambridge CB2 1EW UK
The pharmaceutical industry cares about reducing toxic side effects of drugs in oral formulation. The best solution is to reduce the drug dose. To do so, drugs are required to have high aqueous solubility to ensure good bioavailability.
View Article and Find Full Text PDFACS Nano
January 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China.
Orbital structures are strongly correlated with catalytic performance, whereas their regulation strategy is still in pursuit. Herein, the Fe 3 and O 2 orbital hybridization was optimized by controlling the content of amorphous NiFe(OH) (a-NiFe(OH)), which was grown in situ on crystalline NiFeO (c-NiFeO) using an ultrasonic reduction method. The results of electron energy loss spectroscopy (EELS) and X-ray absorption spectra (XAS) revealed that the Fe-O orbital hybridization in a-NiFe(OH) is effectively strengthened by jointing with the adjacent oxygen (O) in c-NiFeO, which is further confirmed by the higher antibonding orbital energies based on density functional theory (DFT) calculations.
View Article and Find Full Text PDFOptical metasurfaces offer significant advantages in enhancing the speed, efficiency, and miniaturization of imaging systems. However, most existing metasurfaces are limited to static functionalities and lack reconfigurability, which is a key feature for practical applications in dynamic environments. In this work, we demonstrate a reconfigurable optical metasurface capable of switching between two distinct imaging functions (edge detection and bright-field imaging) within the visible spectrum.
View Article and Find Full Text PDFDynamic control of bound states in the continuum (BICs) is usually achieved by engineering structural geometries of lossless optical systems, leading to a passive nature for most current BIC devices. Introducing materials with tunable permittivity, i.e.
View Article and Find Full Text PDFMetasurfaces based on chalcogenide phase-change materials offer a highly promising route towards the realization of non-volatile reconfigurable metasurfaces. However, since their switching mechanism between amorphous and crystalline states is based on thermal stimuli, phase-change metasurfaces should be treated carefully when operating under high power laser sources, since optically induced heating could trigger unwanted state changes during their operation. In this work, therefore, we develop a thermodynamic model capable of tracking the crystallization, melting and reamorphization dynamics of phase-change optical metadevices, and so too their optical performance, when operating under (i.
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