The M/SSZ-39 catalysts (M = In, Co, Cu, Fe) with different metal species and metal loadings were synthesized using the wet impregnation method on a small-pore SSZ-39 molecular sieve. X-ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen adsorption-dehydrogenation and hydrogen temperature program reduction (H-TPR) were employed to characterize the effects of various metal components and metal loadings on the performance of CH selective catalytic reduction of NO reaction (CH-SCR). The characterization results showed that the In/SSZ-39 catalyst exhibited significantly higher catalytic activity compared to the Cu-, Co-, and Fe/SSZ-39 catalysts, suggesting that indium (In) is a more suitable active ingredient for the CH-SCR reaction. The xIn/SSZ-39 (x = 1, 2, 3, x represents the In loadings of 1.0 wt%, 2.0 wt% and 3.0 wt%) catalysts, with different In loadings, all present excellent CH-SCR performance. By varying the In loadings, the type of In species present in the catalyst can be regulated, thus enhancing DeNOx activity and CH selectivity in the CH-SCR reaction. At a low temperature of 400 °C and a low CH/NO feed ratio (CH/NO = 1), the 3In/SSZ-39 catalyst, featuring highly active InOx clusters, achieves the best low-temperature CH-SCR performance, with a high NO conversion rate of up to 90% and a CH selectivity of up to 74.2%.
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http://dx.doi.org/10.3389/fchem.2024.1439581 | DOI Listing |
Chem Sci
December 2024
Department of Chemistry, The Scripps Research Institute 10550N. Torrey Pines Road, La Jolla CA 92037 USA
Catalytic alkene isomerization is a powerful synthetic strategy for preparing valuable internal alkenes from simple feedstocks. The utility of olefin isomerization hinges on the ability to control both positional and stereoisomerism to access a single product among numerous potential isomers. Within base-metal catalysis, relatively little is known about how to modulate reactivity and selectivity with group 6 metal-catalyzed isomerization.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
China University of Petroleum East China, State Key Laboratory of Heavy Oil Processing, 66 The Yangtze River West Road, 266580, Qingdao, CHINA.
The production of hydrogen peroxide (H2O2) through two-electron oxygen reduction reaction (2e- ORR) has emerged as a more environmentally friendly alternative to the traditional anthraquinone method. Although oxidized carbon catalysts have intensive developed due to their high selectivity and activity, the yield and conversion rate of H2O2 under high overpotential still limited. The produced H2O2 was rapidly consumed by the increased intensity of H2O2 reduction, which could ascribe to decomposition of peroxide radicals under high voltage in the carbon catalyst.
View Article and Find Full Text PDFBr J Pharmacol
January 2025
Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
Background And Purpose: Tumour hypoxia frequently presents a major challenge in the treatment of neuroblastoma (NBL). The neuroblastoma cells produce carbonic anhydrase IX (CA IX), an enzyme crucial for the survival of cancer cells in low-oxygen environments.
Experimental Approach: We designed and synthesised a novel high-affinity inhibitor of CA IX.
Parasitol Res
January 2025
Department of Biology, Faculty of Science, Marmara University, Goztepe, 34722, Istanbul, Türkiye.
Babesia bigemina is an apicomplexan parasite responsible for causing "Texas fever" in bovines. Current treatments for bovine babesiosis are hindered by several limitations, including toxicity, insufficient efficacy in eliminating the parasite, and the potential for resistance development. A promising approach to overcome these challenges is the identification of compounds that specifically target essential metabolic pathways unique to the parasite.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Institute of Energy Materials Science (IEMS), University of Shanghai for Science and Technology, Shanghai 200093, China.
Room-temperature sodium-sulfur (RT Na-S) batteries that typically feature multielectron conversion chemistries can allow an ultrahigh specific capacity of 1675 mA h g and a high energy density of 1275 W h kg but unfortunately suffer from a lot of intractable challenges from sulfur cathodes. These issues cover the poor electronic conductivity of pristine sulfur and solid products, the severe shuttle effect of polysulfides, and the sluggish redox kinetics, The shuttling behavior of polysulfides always leads to cathode/anode instability and performance degeneration. Recently, the emerging catalysis strategy has been demonstrated as a reliable pathway to tackle the central issues caused by sulfur electrochemistry and revitalize RT Na-S batteries.
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