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Effect of Steam Treatment on the Catalytic Performance of ZSM-5 in the Co-conversion of Methanol and n-Hexane to Aromatics
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作者 Wei Shumei Xu Yarong +2 位作者 Yang Fan Zhu Kake Zhu Xuedong 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS CSCD 2024年第3期73-81,共9页
Steam pretreatment is a widely used method for modifying the acidity and structure of zeolites,thereby enhancing their catalytic properties.This study systematically investigated the effects of steam treatment on ZSM-... Steam pretreatment is a widely used method for modifying the acidity and structure of zeolites,thereby enhancing their catalytic properties.This study systematically investigated the effects of steam treatment on ZSM-5 zeolites at varying treatment temperatures and durations.The structural evolution of the catalysts was monitored using N2 adsorptiondesorption,X-ray diffraction,inductively coupled plasma optical emission spectroscopy,scanning electron microscopy,NH3 temperature-programmed desorption,in situ pyridine infrared spectroscopy,and thermogravimetric analysis.The characterization results revealed that mesopores were introduced into the ZSM-5 zeolite catalysts through dealumination induced using steam treatment at moderate temperatures(400 and 500℃).Moreover,compared with the parent catalyst,the steam-treated catalysts exhibited a lower amount of acid sites and relative crystallinity,while the n(Si)/n(Al)ratio increased.In the co-conversion of methanol and n-hexane in a fixed bed reactor at 400℃and 0.5 MPa(N2 atmosphere),with a weight hourly space velocity of 1 h−1 and a stoichiometric ratio of 1:1(CH3OH to n-hexane),the steam-treated catalysts displayed a prolonged catalyst lifetime.Particularly,the parent zeolite had a lifetime of 96 h,while the catalyst treated at 500℃for 12 h had a lifetime of up to 240 h.Additionally,the steam-treated catalysts maintained stable n-hexane conversion and improved aromatic selectivity.Notably,these treated catalysts exhibited a lower deactivation rate than the parent catalyst,and would be conducive to industrial scale-up production. 展开更多
关键词 steam ZSM-5 zeolites co-conversion AROMATIZATION METHANOL N-HEXANE
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Gas Chromatography as an Analytical Monitoring Technique for Hydrogen Production from Spirulina maxima 2342
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作者 A. U. Juantorena E. Santoyo +4 位作者 O. Lastres G. Hernández A. Bustos S. A. Gamboa P. J. Sebastian 《Green and Sustainable Chemistry》 2016年第2期78-87,共10页
Hydrogen (H<sub>2</sub>) production from experiments with Spirulina maxima 2342 is reported in this work. The performance of this photosynthetic microorganism for producing H<sub>2</sub> was ev... Hydrogen (H<sub>2</sub>) production from experiments with Spirulina maxima 2342 is reported in this work. The performance of this photosynthetic microorganism for producing H<sub>2</sub> was evaluated for the first time under specific experimental conditions (e.g., a biomass concentration of 0.34 ± 0.02 g, a light intensity of 150 μE.s<sup>-1</sup>.m<sup>-2</sup> and reaction times of 19.3 ± 1.2 h). The performance of this photosynthetic microorganism for producing hydrogen was successfully improved by the addition of sodium dithionite (a reducing agent) as an innovative method for increasing the gas production, and as a main contribution of this work. Quantitative gas chromatography (GC) analyses of H<sub>2</sub> to verify the production performance were successfully carried out at low concentration levels. GC analyses were performed by means of a conventional thermal conductivity detector coupled to a separation system of a Molecular Sieve column 500 mm × 3175 mm (L × ID). Low detection limits were consistently obtained with the GC system used. The separation of H<sub>2</sub> in culture samples was efficiently achieved in average retention times of 1.47 min. The H<sub>2</sub> produced in this process was subsequently used for power generation using a Proton Exchange Membrane Fuel Cell (PEMFC). 展开更多
关键词 Hydrogen Fuel Biological Catalysts photo-biological Production CYANOBACTERIA Fuel Cell Solar Energy
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High‑Temperature Electrochemical Devices Based on Dense Ceramic Membranes for CO_(2) Conversion and Utilization
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作者 Wenping Li Jing‑Li Luo 《Electrochemical Energy Reviews》 SCIE EI 2021年第3期518-544,共27页
The adverse effects of global warming and climate change have driven the exploration of feasible routes for CO_(2) capture,storage,conversion and utilization.The processes related to CO_(2) conversion in high-temperat... The adverse effects of global warming and climate change have driven the exploration of feasible routes for CO_(2) capture,storage,conversion and utilization.The processes related to CO_(2) conversion in high-temperature electrochemical devices(HTEDs)using dense ceramic membranes are particularly appealing due to the simultaneous realization of highly efficient CO_(2) conversion and value-added chemical production as well as the generation of electricity and storage of renewable energy in some cases.Currently,most studies are focused on the two processes,CO_(2) electrolysis and H2O/CO_(2) co-electrolysis in oxygen-conducting solid oxide electrolysis cell(O-SOEC)reactors.Less attention has been paid to other meaningful CO_(2)-conversion-related processes in HTEDs and systematic summary and analysis are currently not available.This review will fill the gap and classify the CO_(2)-conversion-related processes in HTEDs reported in recent years into four types accord-ing to the related reactions,including assisted CO_(2) reduction to CO,H2O and CO_(2) co-conversion,dry reforming of methane and CO_(2) hydrogenation.Firstly,an overview of the fundamentals of HTED processes is presented,and then the related mechanism and research progress of each type of reactions in different HTEDs are elucidated and concluded accordingly.The remaining major technical issues are also briefly introduced.Lastly,the main challenges and feasible solutions as well as the future prospects of HTEDs for CO_(2)-conversion-related processes are also discussed in this review. 展开更多
关键词 Electrochemical devices High temperature CO_(2)reduction co-conversion Dry reforming of methane CO_(2)hydrogenation
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