等离子体辅助甲烷在介质阻挡放电反应器中的非氧化偶联:非催化玻璃材料的影响

IF 3 3区 化学 Q2 CHEMISTRY, APPLIED
Rajesh Kumar Sethi, Mudadla Umamaheswara Rao, Subrahmanyam Challapalli
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引用次数: 0

摘要

采用同轴介质阻挡放电(DBD)作为非热等离子体反应器,在环境条件下实现了甲烷与高级碳氢化合物的非氧化偶联。随后将DBD反应器作为填充床介质阻挡放电,使用非催化材料,包括玻璃微珠、玻璃棉和玻璃毛细管,研究非催化反应机理。典型观察表明,填充DBD的介质玻璃材料可以在不使用任何氧化剂和额外热能的情况下,成功激活稳定的C-H键,生成氢和C2-C4高级碳氢化合物。在所研究的填料中,玻璃毛细管填料的DBD反应器在放电功率为1.38 W, SEI为4.14 J mL−1时,CH4转化率最高为6.1%,能量效率最高为0.66 mmol kJ−1。CH4转化率的提高归因于非催化玻璃材料的等离子体放电行为的改变。此外,在这些条件下,放电区的低温使得等离子体反应器内电极表面的固体碳积累最少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma-Assisted Non-Oxidative Coupling of Methane in a Dielectric Barrier Discharge Reactor: Effect of Non-Catalytic Glass Materials

A coaxial dielectric barrier discharge (DBD) as a non-thermal plasma reactor was utilized for the non-oxidative coupling of methane into higher hydrocarbons under ambient conditions. The DBD reactor was subsequently performed as a packed-bed dielectric barrier discharge using non-catalytic materials, including glass beads, glass wool, and glass capillary, which were introduced to investigate the non-catalytic reaction mechanism. Typical observation demonstrated that the dielectric glass materials packed with DBD might successfully activate the stable C–H bond to produce hydrogen and C2–C4 higher hydrocarbons without the application of any oxidants and additional thermal energy. Among the packing materials investigated, the DBD reactor packed with a glass capillary obtained a maximum CH4 conversion of 6.1%, with the energy efficiency reaching a maximum of 0.66 mmol kJ−1 at a discharge power of 1.38 W with an SEI of 4.14 J mL−1. The enhanced CH4 conversion was attributed to an alternation in the plasma discharge behavior with non-catalytic glass materials. Moreover, under these conditions, the low temperature of the discharge zone resulted in minimal solid carbon accumulation on the inner electrode surface of the plasma reactor.

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来源期刊
Topics in Catalysis
Topics in Catalysis 化学-物理化学
CiteScore
5.70
自引率
5.60%
发文量
197
审稿时长
2 months
期刊介绍: Topics in Catalysis publishes topical collections in all fields of catalysis which are composed only of invited articles from leading authors. The journal documents today’s emerging and critical trends in all branches of catalysis. Each themed issue is organized by renowned Guest Editors in collaboration with the Editors-in-Chief. Proposals for new topics are welcome and should be submitted directly to the Editors-in-Chief. The publication of individual uninvited original research articles can be sent to our sister journal Catalysis Letters. This journal aims for rapid publication of high-impact original research articles in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
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