Reaction mechanism of toluene decomposition in non-thermal plasma: How does it compare with benzene?

IF 6.2 3区 综合性期刊 Q1 Multidisciplinary
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Abstract

Non-thermal plasma (NTP) catalysis is considered one of the most promising technologies to address a wide range of energy and environmental needs, such as carbon dioxide (CO2) conversion, NH3 synthesis, and volatile organic compounds (VOCs) removal. A systematic approach to optimizing NTP systems benefits from understanding VOCs' fundamental NTP destruction behavior and analyzing the correlations between molecular structures and conversion and selectivity. Herein, the mechanical performance of the toluene destruction in NTP is examined and compared with benzene bearing a similar molecular structure. Different experimental and theoretical techniques are applied, including synchrotron vacuum ultraviolet photoionization mass spectrometry(SVUV-PIMS), thermochemistry, and quantum chemistry. Comparatively, toluene is more readily destroyed under the same NTP conditions than benzene. More intriguingly, the distribution of the decomposition species is significantly different. The theoretical calculations reveal that the abundant methyl radicals generated in toluene decomposition mainly lead to the various species distribution. These radicals promote some reactions, such as the decomposition of o-benzoquinone, one of the key intermediates, thus leading to new reaction pathways and products different from benzene. Finally, the critical mechanistic steps of toluene decomposition under the present non-thermal plasma conditions are established, which include the interactions between toluene and electrons or reactive radicals, the cleavage of the aromatic ring, and the various reaction pathways involving of methyl radicals. This study presents an effective approach to elucidate the distinct fundamental reaction mechanisms arising from subtle structural differences, offering new insights into the underlying plasma chemistry crucial for advancing various promising environmental and energy applications of non-thermal plasma systems.
甲苯在非热等离子体中分解的反应机理:与苯相比如何?
非热等离子体(NTP)催化技术被认为是最有前途的技术之一,可满足二氧化碳(CO2)转化、NH3 合成和挥发性有机化合物(VOCs)去除等广泛的能源和环境需求。了解挥发性有机化合物的基本 NTP 破坏行为并分析分子结构与转化率和选择性之间的相关性,是优化 NTP 系统的系统性方法。本文研究了甲苯在 NTP 中破坏的机械性能,并与具有类似分子结构的苯进行了比较。研究采用了不同的实验和理论技术,包括同步辐射真空紫外光电离质谱法(SVUV-PIMS)、热化学和量子化学。在相同的 NTP 条件下,甲苯比苯更容易被破坏。更有趣的是,分解物种的分布也有很大不同。理论计算显示,甲苯分解过程中产生的大量甲基自由基主要导致了各种物种的分布。这些自由基促进了一些反应,如关键中间产物之一邻苯醌的分解,从而导致了不同于苯的新反应途径和产物。最后,确定了甲苯在当前非热等离子体条件下分解的关键机理步骤,其中包括甲苯与电子或活性自由基之间的相互作用、芳香环的裂解以及涉及甲基自由基的各种反应途径。这项研究提出了一种有效的方法来阐明因微妙的结构差异而产生的不同的基本反应机制,为了解潜在的等离子体化学提供了新的视角,这对于推动非热等离子体系统在环境和能源领域的各种应用前景至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fundamental Research
Fundamental Research Multidisciplinary-Multidisciplinary
CiteScore
4.00
自引率
1.60%
发文量
294
审稿时长
79 days
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