The ability to measure and predict molecular diffusion coefficients in multicomponent mixtures is not only of fundamental scientific interest but also of significant relevance in understanding how catalytic processes proceed. In the present work, the direct measurement of the molecular diffusion of H and CO gas-phase species diffusing in -alkane mixtures using pulsed-field gradient (PFG) nuclear magnetic resonance (NMR) methods is reported. The work is of direct relevance to Fischer-Tropsch (FT) catalysis, with the measurements being made of the gas-wax system with the wax in both the bulk liquid state and when confined within a titania catalyst support, at temperatures and pressures typical of low-temperature FT synthesis. Molecular diffusion coefficients of H and CO within wax-saturated porous titania in the range (1.00-2.43) × 10 and (6.44-8.50) × 10 m s, respectively, were measured in the temperature range of 140-240 and 200-240 °C for H and CO, respectively, at a pressure of 40 bar. The wax mixture was typical of a wax produced during FT catalysis and had a molar average carbon number of 36. It is shown that the hydrogen diffusion coefficient within this wax mixture is consistent, to within experimental error, with the hydrogen diffusion coefficient measured in pure single-component -hexatriacontane (-C) wax; this result held with the waxes in the bulk liquid state and when confined within the porous titania. The tortuosity of the porous titania was also measured using PFG NMR and found to be 1.77; this value is independent of temperature. The ability of existing correlations to predict these experimentally determined data was then critically evaluated. Although the Wilke-Chang correlation was found to underestimate the molecular diffusion coefficients of both H and CO diffusing in the wax in both the bulk state and when confined within the porous titania, parameterized correlations based on the rough hard sphere model, having accounted for the experimentally determined tortuosity factor, predicted the H and CO diffusion within bulk and confined wax to within 3%.
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http://dx.doi.org/10.1021/acs.jpcb.0c07440 | DOI Listing |
PLoS One
January 2025
Department of Crop and Soil Sciences, College of Agricultural and Environmental Sciences, University of Georgia, Griffin, Georgia, United States of America.
Previous studies have indicated the great performance of electrooxidation (EO) to mineralize per- and polyfluoroalkyl substances (PFASs) in water, but different anions presented in wastewater may affect the implementation of EO treatment in field applications. This study invetigated EO treatment of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA), two representative perfluoroalkyl acids (PFAAs), using porous Magnéli phase titanium suboxide anodes in electrolyte solutions with different anions present, including NO3-, SO42-, CO32- and PO43-. The experiment results indicate that CO32- enhanced PFAS degradation, while NO3- suppressed the degradation reactions with its concentration higher than 10 mM.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Department of Chemistry, College of Natural and Mathematical Sciences, The University of Dodoma, P.O Box 259, Dodoma, Tanzania. Electronic address:
In this study, a highly crystalline anatase/rutile mixed phase carrageenan/TiO nanocomposite with a larger surface area was synthesized via the sol-gel process and calcined at 450 °C and 650 °C. The synthesized composite materials were characterized by FTIR, XRD, SEM, EDX, TEM, BET and TGA. FTIR confirms the presence of C-Ti-O bond formation in composite.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Process Engineering Division, CSIR-Central Electrochemical Research Institute, Karaikudi, Tamilnadu 630003, India.
The present study aims to analyze the thermal regulation of the Ce/Ce ratio on the nanonetwork titania layer over the titanium (Ti) surface developed by the alkali-mediated surface modification approach. The effect of sequential heat treatment from 200 to 800 °C was evaluated for its surface characteristics such as morphology, phase formation, roughness, hardness, hydrophilicity, etc. Surface oxidation by temperatures up to 600 °C demonstrated a progressive increase in the Ce (CeO) content with a rutile TiO network layer over the Ti surface.
View Article and Find Full Text PDFMaterials (Basel)
December 2024
Institute of Materials and Surface Engineering, Faculty of Natural Science and Technology, Riga Technical University, Paula Valdena st. 3/7, LV-1048 Riga, Latvia.
Sintered porous mullite-alumina ceramics are obtained from the concentrated suspension of powdered raw materials such as kaolin, gamma and alpha AlO, and amorphous SiO, mainly by a solid-state reaction with the presence of a liquid phase. The modification of mullite ceramic is achieved by the use of micro- and nanosize TiO powders. The phase compositions were measured using an X-ray powder diffraction (XRD) Rigaku Ultima+ (Tokyo, Japan) and microstructures of the sintered specimens were analysed using scanning electron microscopy (SEM) Hitachi TM3000-TableTop (Tokyo, Japan).
View Article and Find Full Text PDFMaterials (Basel)
November 2024
Osipyan Institute of Solid State Physics of the Russian Academy of Sciences, Ac. Osipyan Str. 2, 142432 Chernogolovka, Russia.
The simple oxides like titania, zirconia, and ZnO are famous with their antibacterial (or even antimicrobial) properties as well as their biocompatibility. They are broadly used for air and water filtering, in food packaging, in medicine (for implants, prostheses, and scaffolds), etc. However, these application fields can be broadened by switching to the composite multicomponent compounds (for example, titanates) containing in their unit cell, together with oxygen, several different metallic ions.
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