The conversion of methane, CH, into higher value chemicals using low temperature plasmas is challenged by both improving efficiency and selectivity. One path toward selectivity is capturing plasma-produced methyl radicals, CH, in a solvent for aqueous processing. Due to the rapid reactions of methyl radicals in the gas phase, the transport distance from the production of the CH to its solvation should be short, which then motivates the use of microplasmas. The generation of CH in Ar/CH/HO plasmas produced in nanosecond pulsed dielectric barrier discharge microplasmas is discussed using results from a computational investigation. The microplasma is sustained in the channel of a microfluidic chip in which the solvent flows along one wall or in droplets. CH is primarily produced by electron-impact of and dissociative excitation transfer to CH, as well as CH reacting with CH. CH is rapidly consumed to form CH which, in spite of being subject to these same dissociative processes, accumulates over time, as do other stable products including CH and CHOH. The gas mixture and electrical properties were varied to assess their effects on CH production. CH production is largest with 5% CH in the Ar/CH/HO mixture due to an optimal balance of electron-impact dissociation, which increases with CH percentage, and dissociative excitation transfer and CH reacting with CH, which decreases with CH percentage. Design parameters of the microchannels were also investigated. Increasing the permittivity of the dielectrics in contact with the plasma increased the ionization wave intensity, which increased CH production. Increased energy deposition per pulse generally increases CH production as does lengthening pulse length up to a certain point. The arrangement of the solvent flow in the microchannel can also affect the CH density and fluence to the solvent. The fluence of CH to the liquid solvent is increased if the liquid is immersed in the plasma as a droplet or is a layer on the wall where the ionization wave terminates. The solvation dynamics of CH with varying numbers of droplets was also examined. The maximum density of solvated methyl radicals CH occurs with a large number of droplets in the plasma. However, the solvated CH density can rapidly decrease due to desolvation, emphasizing the need to quickly react with the solvated species in the solvent.
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http://dx.doi.org/10.1021/acs.jpca.4c00073 | DOI Listing |
Int J Biol Macromol
January 2025
Beijing Key Laboratory of Lignocellulosic Chemistry, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China. Electronic address:
Due to the emphasis on the environmental and health issues caused by petroleum-based plastics, renewable lignocellulosic materials emerge as promising substitutes. However, their practical application remains hindered by unsatisfactory properties such as fragility and sensitivity to water. Dealing with the challenge of non-thermal processing of xylan and addressing the issue of performance degradation resulting from the hygroscopicity of materials.
View Article and Find Full Text PDFBiochemistry
January 2025
Department of Pharmaceutical Sciences, University of Shizuoka, Shizuoka 422-8526, Japan.
DtpC was isolated from the ditryptophenaline biosynthetic pathway found in filamentous fungi as a cytochrome P450 (P450) that catalyzes the dimerization of diketopiperazines. More recently, several similar P450s were discovered. While a vast majority of such P450s generate asymmetric diketopiperazine dimers, DtpC and other fungal P450s predominantly catalyze the formation of symmetric dimer products.
View Article and Find Full Text PDFEnviron Sci Process Impacts
January 2025
Univ. Lille, CNRS, UMR 8522, Physico-Chimie des Processus de Combustion et de l'Atmosphère - PC2A, 59000 Lille, France.
Fenpyrazamine (FPA) is a widely used fungicide in agriculture to control fungal diseases, but its environmental degradation by oxidants and the formation of potential degradation products remain unexplored. This study investigates the oxidation of FPA by hydroxyl radicals (HO˙) using density functional theory (DFT) calculations at the M06-2X/6-311++G(3df,3pd)//M06-2X/6-31+G(d,p) level of theory. Three standard oxidation mechanisms, including formal hydrogen transfer (FHT), radical adduct formation (RAF), and single electron transfer (SET), were evaluated in the aqueous phase, with reaction kinetics analyzed over a temperature range of 283-333 K.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
School of Chemistry, Xi'an Jiaotong University, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an 710049, China.
Herein, SUMO-LUMO inversion (SLI) radicals - were designed by the combination of the tris(2,4,6-trichlorophenyl)methyl (TTM) radical and pyridinium derivatives (electron-withdrawing groups) for the first time. The energy of the LUMO lies below that of the SUMO, which deviated from the Aufbau principle as an alternative electronic configuration beyond the well-established SOMO-HOMO inversed system. Thus, for SLI radicals, the injection of one extra electron preferred to occupy the LUMO rather than the SUMO, giving diradicals, one of which had been fully confirmed by single crystal analysis, VT-NMR and VT-EPR experiments, as well as DFT calculations.
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