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Treating perfluorooctanoic acid (PFOA) in an aqueous environment is problematic due to its low concentration and its high resistance to biological and chemical degradation. To tackle this challenge, combinations of pre-enrichment and photodegradation processes are promising solutions. In this work, we investigated metal ion-exchanged zeolites as adsorbents and photocatalysts for PFOA treatment. Among various transition metal ion-exchanged BEA zeolites, Fe-exchanged BEA (Fe-BEA) zeolites showed significant activity for the photodegradation of PFOA. The isolated iron species in Fe-BEA zeolite are responsible for PFOA photodegradation, whereas other iron species present from excess iron loading in the zeolite will lower its photocatalytic activity. Furthermore, it was proved via size exclusion tests using branched PFOA isomers that the photodegradation of PFOA took place on the internal surface rather than the external surface of Fe-BEA zeolite. Photodegradation of PFOA was also tested to be effective with Fe-exchanged BEA-type zeolites having various SiO/AlO ratios, but ineffective with FAU-type zeolites. The optimal Fe-BEA zeolite showed a sorption coefficient of 6.0 × 10 L kg at an aqueous phase PFOA concentration of 0.7 μg L and a PFOA half-life of 1.8 h under UV-A irradiation. The presented study offers a deeper understanding of the use of metal ion-exchanged zeolites for photodegradation of PFOA.
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http://dx.doi.org/10.1021/acsestengg.3c00462 | DOI Listing |
Inorg Chem
August 2025
Research Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
We systematically explored the formation range of α-NaFeO-type layered titanate and its ion-exchange behaviors and electrochemical performance. The layered sodium titanate of NaTiLiO at = 0.68-0.
View Article and Find Full Text PDFNat Commun
May 2025
Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts, USA.
Sorbents capable of cycling water vapor under dry conditions are critical for applications such as atmospheric water harvesting, desiccation, and heat pumps; however, few existing sorbents demonstrate both hysteresis-free behavior and cycling stability. Here we show that post-synthetic exchange with lithium, sodium, potassium, magnesium, and tetramethylammonium in the metal-organic framework (MOF) SU-102 ([(CH)NH][Zr(HL)]; HL = ellagic acid) enables high-capacity water sorption under low humidity ranging from 11.1% to 4.
View Article and Find Full Text PDFSensors (Basel)
April 2025
Dukhov Automatics Research Institute (VNIIA), 22 Sushchevskaya St., 127055 Moscow, Russia.
Here, we study the fluorescence response of neutrophils stained with the wheat germ agglutinin Alexa Fluor 594 dye when the cells are placed on plasmonic nanoparticle substrates. Specifically, we focused on gold and silver nanoparticles with particle sizes ranging from 12 to 250 nm. It was demonstrated that the intensity of fluorescence can be increased by more than 10 times when using substrates with silver nanoparticles formed by Na-Ag ion exchange in glass.
View Article and Find Full Text PDFChemistry
May 2025
TUM School of Natural Sciences, Department Chemie, Technische Universität München, Lichtenbergstraße 4, Garching, Germany.
Zintl phases are excellent precursors for nine atom [E] clusters, which are readily accessible by dissolution of AE phases (A = Na-Rb; E = Ge-Pb) in ethylenediamine (en). In contrast, the binary alkali-metal tetrel phases of composition AE are insoluble in en. Furthermore, Li cations are rarely investigated as counterions for tetrel element Zintl clusters.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Department of Chemistry, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
Efficient separation of hydrogen isotopes, especially deuterium (D), is pivotal for advancing industries such as nuclear fusion, semiconductor processing, and metabolic imaging. Current technologies, including cryogenic distillation and Girdler sulfide processes, suffer from significant limitations in selectivity and cost-effectiveness. Herein, we introduce a novel approach utilizing an imidazolium-based Metal-Organic Framework (MOF), JCM-1, designed to enhance D/H separation through temperature-dependent gate-opening controlled by ion exchange.
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