We demonstrate the successful functionalization of a porous aromatic framework for uranium extraction from water as exemplified by grafting PAF-1 with the uranyl chelating amidoxime group. The resultant amidoxime-functionalized PAF-1 (PAF-1-CHAO) exhibits a high uranium uptake capacity of over 300 mg g and effectively reduces the uranyl concentration from 4.1 ppm to less than 1.0 ppb in aqueous solutions within 90 min, well below the acceptable limit of 30 ppb set by the US Environmental Protection Agency. The local coordination environment of uranium in PAF-1-CHAO is revealed by X-ray absorption fine structure spectroscopic studies, which suggest the cooperative binding between UO and adjacent amidoxime species.
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http://dx.doi.org/10.1021/acsami.7b01711 | DOI Listing |
The carbon dioxide (CO) capture and utilization strategy has emerged as an innovative and multifaceted approach to counteract carbon emissions. In this study, a highly porous muffin polyhedral barium (Ba) ̵ organic framework (BaTATB; HTATB = 4,4',4″--triazine-2,4,6-triyl-tribenzoic acid) was synthesized solvothermally. The three-dimensional honeycomb pore architectures were densely populated with Lewis acidic Ba(II) metal sites and basic nitrogen-rich triazines.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
College of Natural Resources and Environment, Northwest A&F University, Yangling 712100, China; Key Laboratory of Plant Nutrition and the Agro-environment in Northwest China, Ministry of Agriculture, Yangling 712100, China. Electronic address:
The interactions between microplastic-derived dissolved organic matter (MPs-DOM) and heavy metals (Cu, Pb, and Cd) regulate the complex environmental transport behavior of pollutants in terrestrial and aquatic environments. In this study, fluorescence excited emission matrix spectroscopy combined with parallel factor analysis (EEM-PARAFAC) and electrospray ionization coupled Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS) were employed to investigate the complexation mechanism of MPs-DOM with heavy metals, as well as the effects of different environmental occurrences of MPs-DOM on the transport behaviors of heavy metals in saturated porous medium. The findings demonstrated that MPs-DOM, particularly humic-like substances containing aromatic structures and various oxygen functional groups, could form stable complexes with heavy metals.
View Article and Find Full Text PDFChem Asian J
January 2025
Qingdao University of Science and Technology, College of Polymer Science and Engineering, 53 ZHENGZHOU ROAD, 266000, Qingdao, CHINA.
Constructing highly conjugated three-dimensional covalent organic frameworks (3D COFs), particularly those with luminescent features, remains a significant challenge. In this work, we successfully synthesized a 3D COF, named 3D-Py-SP-COF, using a rigid and orthogonal spirobifluorene building block for the spatial 3D structure construction and planar pyrene as luminescent units. The incorporation of the pyrene and the unique rigid 3D network structure endow 3D-Py-SP-COF with fluorescent properties.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Tsinghua University, Institute of Nuclear and New Energy Technology, Room A320, Nengke Building, Qinghua Yuan No.1, Beijing, CHINA.
Exploiting supramolecular secondary building units (SSBUs) for developing porous crystalline materials represents an exciting breakthrough that extends the boundaries of reticular chemistry. However, shaping polynuclear clusters sustained by non-covalent interactions for the assembly of hydrogen-bonded frameworks remains a critical challenge. This study presents a novel strategy to stabilize SSBUs by tuning the π-stacking geometry of conjugated building blocks, facilitating the creation of hydrogen-bonded frameworks with tailored architectures for demanding gas separation.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Chemistry, Netaji Subhas University of Technology, Delhi, India.
Nanoporous organic polymers (NPOPs) have emerged as versatile materials with robust thermal stability, large surface area (up to 2500 m g), and customizable porosity, making them ideal candidates for advanced hydrogen (H) storage applications. This review provides a comprehensive analysis of various NPOPs, including covalent organic frameworks (COFs), hypercrosslinked polymers (HCLPs), conjugated microporous polymers (CMPs), and porous aromatic frameworks (POAFs). Notably, these materials demonstrate superior H storage capacities, achieving up to 10 wt% at cryogenic temperatures, which is essential for applying H as a clean energy carrier.
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