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A highly efficient growth mechanism of polycyclic aromatic hydrocarbons. | LitMetric

A highly efficient growth mechanism of polycyclic aromatic hydrocarbons.

Phys Chem Chem Phys

The Department of Chemical System Engineering, The University of Tokyo, 7-3-1, Bunkyo-ku, Hongo, Tokyo 113-8656, Japan.

Published: March 2010

AI Article Synopsis

  • The study investigates the growth mechanism of polycyclic aromatic hydrocarbons (PAHs), focusing on how phenyl radicals enhance this process during the pyrolysis of benzene, both alone and with acetylene.
  • Using advanced mass spectrometry, researchers detected a range of PAH products, identifying patterns in mass peaks that reflect the formation and transformation of phenyl-PAHs and other PAH structures as temperature increased.
  • The analysis indicates that phenyl addition/cyclization (PAC) is a more efficient pathway for PAH growth compared to the hydrogen abstraction/C(2)H(2) addition (HACA) mechanism, especially when acetylene is mixed with benzene, leading to higher production of phenyl-containing PA

Article Abstract

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.

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Source
http://dx.doi.org/10.1039/b919644gDOI Listing

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