Liang Yuting, Xue Yingying, Fang Dongxu, Tan Ting, Jiang Zhi, Shangguan Wenfeng, Yang Jiuzhong, Pan Yang
Research Center for Combustion and Environmental Technology, Shanghai Jiao Tong University, Shanghai 200240, China.
Laboratory of Theoretical and Computational Nanoscience, CAS Key Laboratory of Nanophotonic Materials and Devices, National Center for Nanoscience and Technology, Chinese Academy of Sciences, Beijing 100190, China.
Fundam Res. 2022 May 2;4(5):1100-1109. doi: 10.1016/j.fmre.2022.03.026. eCollection 2024 Sep.
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 (CO) conversion, NH 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.
非热等离子体(NTP)催化被认为是满足广泛能源和环境需求的最具前景的技术之一,例如二氧化碳(CO)转化、NH合成以及挥发性有机化合物(VOCs)去除。优化NTP系统的系统方法受益于了解VOCs的基本NTP破坏行为以及分析分子结构与转化率和选择性之间的相关性。在此,研究了NTP中甲苯破坏的机械性能,并与具有相似分子结构的苯进行了比较。应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(SVUV-PIMS)、热化学和量子化学。相比之下,在相同的NTP条件下,甲苯比苯更容易被破坏。更有趣的是,分解产物的分布有显著差异。理论计算表明,甲苯分解过程中产生的大量甲基自由基主要导致了各种产物分布。这些自由基促进了一些反应,如关键中间体之一邻苯醌的分解,从而导致了与苯不同的新反应途径和产物。最后,确定了当前非热等离子体条件下甲苯分解的关键机理步骤,包括甲苯与电子或活性自由基之间的相互作用、芳环的裂解以及涉及甲基自由基的各种反应途径。本研究提出了一种有效的方法来阐明由细微结构差异引起的独特基本反应机理,为推进非热等离子体系统各种有前景的环境和能源应用至关重要的潜在等离子体化学提供了新的见解。