The Department of Chemical System Engineering, The University of Tokyo, 7-3-1, Bunkyo-ku, Hongo, Tokyo 113-8656, Japan.
Phys Chem Chem Phys. 2010 Mar 14;12(10):2427-37. doi: 10.1039/b919644g. Epub 2010 Jan 21.
A highly efficient growth mechanism of polycyclic aromatic hydrocarbons (PAHs) initiated and accelerated by phenyl radicals has been investigated on the basis of kinetic analysis of gas phase reaction products of pyrolysis of benzene with and without addition of acetylene and acetylene only. Pyrolytic reactions were performed in a flow tube reactor and the resulting products were detected by an in situ direct sampling mass spectrometric technique using a vacuum ultraviolet (VUV) single photon ionization (SPI) time of flight mass spectrometry (TOFMS). The detected species varies from smaller to larger PAHs up to m/z = 454 (C(36)H(22)) including primary PAHs, polyphenyl-PAHs and cyclopentafused-PAHs (CP-PAHs). The peculiarity of this result is an appearance of mass peaks at regular mass number intervals of approximately 76 that correspond to phenyl-PAHs produced by phenyl radical addition (+C(6)H(5), +77) followed by hydrogen elimination (-H, -1). All such mass peaks were found diminishing with appearance of -2 mass number peaks with increasing temperatures, certainly due to a conversion of thermally rather unstable phenyl-PAHs into stable condensed PAHs through a dehydrocyclization (-H(2), -2) process. In the same way, in the case of only acetylene pyrolysis, mass peaks at regular mass number intervals of 24 corresponding to the HACA (hydrogen abstraction/C(2)H(2) addition) products, were observed. Kinetic analysis of formation pathways of those observed products showed the active role of PAC (phenyl addition/cyclization) because of its efficiency to continue the endless growth of PAHs, while the HACA was only found efficient for producing symmetrical PAHs by filling a triple fusing site (four carbon bay structure). Especially, acetylene was mixed with benzene to understand the impact of HACA on the PAC path ways that resulted in enhancement of phenyl-PAHs production in spite of trapping of active and chain carrier species phenyl radicals by C(2)H(2) to form phenylacetylene. The comparison of HACA and PAC concluded that PAC is a highly efficient mechanism for the growth of PAHs and lastly their combined roles in combustion have been discussed. Hopefully, PAC will be useful to understand the process of aromatic growth, from furnaces to stellar atmospheres.
已基于苯热解过程中气相反应产物的动力学分析,研究了由苯基自由基引发和加速的多环芳烃(PAHs)的高效生长机制,该分析研究中包括苯与乙炔的混合物以及纯乙炔。热解反应在流动管反应器中进行,通过使用真空紫外(VUV)单光子电离(SPI)飞行时间质谱(TOFMS)的原位直接采样质谱技术检测生成的产物。所检测的物质从较小的 PAHs 到较大的 PAHs 不等,质量数高达 m/z = 454(C(36)H(22)),包括初级 PAHs、多苯基-PAHs 和环戊并-PAHs(CP-PAHs)。该结果的特点是,出现了质量数以大约 76 的间隔规则分布的质量峰,这些质量峰对应于通过苯基自由基加成(+C(6)H(5),+77)和随后的氢消除(-H,-1)产生的苯基-PAHs。所有这些质量峰都随着温度的升高而减少,这肯定是由于通过脱氢环化(-H(2),-2)过程,热稳定性较差的苯基-PAHs 转化为稳定的缩合 PAHs。同样,在仅乙炔热解的情况下,观察到质量数以 24 的间隔规则分布的质量峰,这些质量峰对应于 HACA(氢提取/C(2)H(2)加成)产物。对观察到的产物形成途径的动力学分析表明,由于其能够使 PAHs 不断生长,PAC(苯基加成/环化)具有重要作用,而 HACA 仅通过填充三重融合位点(四个碳湾结构)有效地用于生成对称 PAHs。特别是,将乙炔与苯混合,以了解 HACA 对 PAC 途径的影响,结果是尽管 C(2)H(2)捕获了活性和链载物种苯基自由基,但仍增加了苯基-PAHs 的生成。HACA 和 PAC 的比较得出结论,PAC 是 PAHs 生长的高效机制,最后讨论了它们在燃烧中的联合作用。希望 PAC 将有助于了解从熔炉到恒星大气的芳香族生长过程。