A series of functionalized metal organic frameworks (MOFs) were synthesized by the post-synthetic modification (PSM) of Zr(iv)-containing UiO-66-NH MOFs using covalent grafting with various functional groups utilizing pendant -NH moieties. The tethering of amide (with/without pendant carboxylic acid), iminopyridine, phoshinic amide and sulphur-containing functionalities produced a library of eight different UiO-66-NH derivatives. The functionalized MOFs were characterized by FT-IR spectroscopy, NMR, PXRD, TGA, SEM-EDX and BET surface area analysis. Uranyl ion extraction with the functionalized MOFs was investigated in acidic/neutral/basic conditions (pH 1 to 9). This work presents a comprehensive study of different functionalized MOFs to investigate the effects of various analytical parameters, including pH, contact time, and desorption process. The MOFs as solid phase extractants (SPEs) provide a direct comparison of the sorption efficiencies of different functional groups on a common solid support. A phosphorous-functionalized material, UiO-66-PO-Ph, with enhanced thermal stability (∼500 °C) exhibits the best sorption capacity (∼96%) in an acidic medium (pH 3). The parent MOF UiO-66-NH (92%) and iminopyridine-functionalized UiO-66-IMP (90%) showed excellent sorption in neutral conditions (pH 7). Amide-containing MOFs UiO-66-AM1 (40%), UiO-66-AMMal (31%) and UiO-66-AMGlu (70%), sulfur-based MOFs UiO-66-SMA (65%) and UiO-66-SSA (27%), and phosphorous-functionalized UiO-66-PO-OPh (50%) displayed maximum sorption in basic conditions (pH 8). The kinetics studies revealed rapid uranium sorption in about 2 h due to the effective binding of uranyl ions with the anchored functional groups of MOFs; quantitative elution of uranyl ions from the MOF framework was carried out with 0.1/0.01 M HNO. The MOFs also exhibit moderate recyclability for uranium sorption and can be regenerated by an acidic solution. The functionalized MOFs alter the stability in acidic/basic media; thus, UiO-66-NH is a versatile MOF material employed as an SPE for the extraction of radionuclides from aqueous media. This work also provides a platform for the development of new functionalized MOF materials for the efficient sorption of uranium as well as moderate recyclability for its removal, and the potential applications include the removal of uranium from aqueous waste streams.
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http://dx.doi.org/10.1039/d0ra00410c | DOI Listing |
Mikrochim Acta
January 2025
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science, Northwest University, Xi' an, 710069, PR, China.
Thiazolo[5,4-d]thiazole-2,5-dicarboxylic acid (HThz), a thiazolothiazole (TTz) derivative with carboxylic acid groups, was synthesized as a ligand for the creation of five MOFs, each associated with distinct metal ions including Ag, Mn, Co, Zn, and Cu. The cathodic electrochemiluminescence (ECL) of HThz and the resulting MOFs was investigated. HThz was found to generate ECL signals, but this process was heavily reliant on potassium persulfate (KSO) as a co-reactant.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001, P. R. China.
Defective MOFs have been identified as promising candidates for efficient membrane-based separation applications. However, the utilization of defective MOFs in membrane gas separation is still in its infancy due primarily to the inefficient molecular differentiation induced by structural defects. Herein, we report a strategic combination of ionic liquid (IL) and defective UiO-66-NH MOF to ameliorate the CO/N selectivity within the highly permeable PIM-1 polymer.
View Article and Find Full Text PDFSmall
January 2025
School of Materials and Chemical Engineering, Chuzhou University, Chuzhou, 239000, China.
Effectual CH reclamation from CH/N blends by existing physisorbents in industrialization confronts the adversity of frustrated separation performance, weak structural strength, and restricted scale-up preparation. To solve aforesaid bottlenecks, herein, a strategy is presented to fabricate synergistic strong recognition binding sites in a robust and scalable optimum Cu(pma) with ultramicroporous feature regarding superb CH separation versus N. By virtue of the synergistic contribution of multiple affinities accompanied by enormous potential field overlap of pore restriction, it imparts strong recognition binding toward CH molecules.
View Article and Find Full Text PDFSmall
January 2025
Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, School of Materials Science and Engineering, Hubei University, Wuhan, 430062, P. R. China.
Innovative design strategies of fog harvesting devices (FHDs) demonstrate promising remedy for water crisis in arid areas. 1D FHDs ensure unimpeded wind circulation and can be manufactured more cost-effectively for extensive regions. Inspired by cactus thorns, desert beetles, and spider silk, two metal organic frameworks (MOFs) functionalized Cu wires with opposite wettability are double-twisted by a mechanical twisting machine, forming 1D double-spiral Cu wires with alternating superhydrophobic/superhydrophilic dual-MOF patterns.
View Article and Find Full Text PDFSmall
January 2025
School of Materials Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education), Tianjin University, Tianjin, 300072, China.
Enhancing the catalytic performance and durability of M-N─C catalyst is crucial for the efficient operation of proton exchange membrane fuel cells (PEMFCs) and Zn-Air batteries (ZABs). Herein, an approach is developed for the in situ fabrication of a MOFs-derived porous carbon material, co-loaded with Co nanoparticles (NPs) and Co-N sites and integrated onto Fe-doped carbon nanotubes (CNTs), named Co-NC/Fe-NCNTs. Incorporating polymer-wrapped CNTs improves MOFs dispersion annealing at high temperature, which amplifies the three-phase boundary (TPB) by generating much more mesopores and exposing additional active sites within the catalysts layer.
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