The performance of many chemical gas-phase reactions is strongly influenced by the interaction of reactants with interfaces. Nanoporous materials, which exhibit pore diameters up to 100 nm and high specific surface areas, can be utilized to reduce the amount of cost-intensive materials (e.g. noble metals). However, due to limitations in material transport and reaction kinetics detailed knowledge of the diffusion and the kinetics of a chemical reaction is necessary to improve the performance of chemical processes in industry and research. To experimentally study the diffusion and reaction kinetics of gaseous species inside such pores, the chemoresistive behavior of certain metal oxides such as InO can be utilized. In this work, we present a model system based on hierarchically porous monolithic indium oxide (InO) which allows the determination of kinetic effects by utilizing its gas transducing properties. The experimental data obtained by electrical measurements are compared to two diffusion and diffusion-reaction models. Using these methods, the rate constant of ozone decomposition in porous InO is estimated. The results are the basis for a suitable material design for semiconducting gas sensors, on the nano-, meso- and macroscale, which helps in understanding the underlying mechanisms of diffusion and reaction.
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http://dx.doi.org/10.1039/c6cp08874k | DOI Listing |
J Phys Chem A
January 2025
Centro de Bioinformática, Simulación y Modelado (CBSM), Departamento de Bioinformática, Facultad de Ingeniería, Universidad de Talca, Talca 3465548, Chile.
In this research, we investigated the essential role of biogenic volatile organic compound emissions in regulating tropospheric ozone levels, atmospheric chemistry, and climate dynamics. We explored linalool ozonolysis and secondary organic aerosol formation mechanisms, providing key insights into atmospheric processes. Computational techniques, such as density functional theory calculations and molecular dynamics simulations, were employed for the analysis.
View Article and Find Full Text PDFFoods
December 2024
State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou 310027, China.
Developing and implementing technologies that can significantly reduce food loss during storage and transport are of paramount importance. Ozone synergistic catalytic oxidation (OSCO) technology has been developed, which sterilizes bacteria and viruses on the surface of food and degrades ethylene released during fruit storage through the active oxygen produced by the catalytic decomposition of ozone. Herein, we report the hydrothermal synthesis of MnO with distinct phase compositions and nanostructures through simply varying the reaction temperatures.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China; Key Laboratory of New Low-carbon Green Chemical Technology, Education Department of Guangxi Zhuang Autonomous Region, Nanning 530004, China. Electronic address:
Front Microbiol
December 2024
College of Forestry, Gansu Agricultural University, Lanzhou, China.
Alpine wet meadows are known as NO sinks due to nitrogen (N) limitation. However, phosphate addition and N deposition can modulate this limitation, and little is known about their combinative effects on NO emission from the Qinghai-Tibet Plateau in wet meadows. This study used natural wet meadow as the control treatment (CK) and conducted experiments with N (CONH addition, N15), P (NaHPO addition, P15), and their combinations (CONH and NaHPO addition, N15P15) to investigate how N and P supplementation affected soil NO emissions in wet meadow of QTP.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemical Engineering, Virginia Tech, Blacksburg, Virginia 24061, United States.
The decomposition of ozone on supported manganese oxide catalysts, studied here, exemplifies reactions involving electron transfer. In situ extended X-ray absorption fine-structure spectra (Mn K-edge) on in situ treated samples show that the supported phase in MnO/SiO resembles MnO while that in MnO/AlO samples resembles MnO. In situ Raman spectroscopy shows the involvement of a common peroxide surface species.
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