論文

査読有り
2014年7月

Reflectance spectroscopy (350-2500 nm) of solid-state polycyclic aromatic hydrocarbons (PAHs)

ICARUS
  • M. R. M. Izawa
  • ,
  • D. M. Applin
  • ,
  • L. Norman
  • ,
  • E. A. Cloutis

237
開始ページ
159
終了ページ
181
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.icarus.2014.04.033
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

Polycyclic aromatic hydrocarbons (PAHs) are organic compounds based on fused aromatic rings, and are formed in a variety of astrophysical, solar nebula and planetary processes. Polycyclic aromatic hydrocarbons are known or suspected to occur in a wide variety of planetary settings including icy satellites, Titan's hazes, carbonaceous meteorites, comet nuclei, ring particles; and terrestrial organic-rich lithologies such as coals, asphaltites, and bituminous sands. Relatively few measurements of the visible and near-infrared spectra of PAHs exist, yet this wavelength region (350-2500 nm) is widely used for remote sensing. This study presents detailed analyses of the 350-2500 nm reflectance spectra of 47 fine-grained powders of different high-purity solid-state PAHs. Spectral properties of PAHs change with variations in the number and connectivity of linked aromatic rings and the presence and type of side-groups and heterocycles. PAH spectra are characterized by three strong features near similar to 880 nm, similar to 1145 nm, and similar to 1687 nm due to overtones of vCH fundamental stretching vibrations. Some PAHs are amenable to remote detection due to the presence of diagnostic spectral features, including: N-H stretching overtones at 1490-1515 nm in NH- and NH2-bearing PAHs, aliphatic or saturated bond C-H overtone vibrations at,similar to 1180-1280 nm and,similar to 1700-1860 nm; a broad asymmetric feature between similar to 1450 nm and similar to 1900 nm due to O-H stretching overtones in aromatic alcohols, C-H and C=0 combinations near similar to 2000-2010 nm and similar to 2060-2270 nm in acetyl and carboxyl-bearing PAHs. Other substituents such as sulphonyl, thioether ether and carboxyl heterocycles, or cyano, nitrate, and aromatic side groups, do not produce well-resolved diagnostic spectral features but do cause shifts in the positions of the aromatic C-H vibrational overtone features. Fluorescence is commonly suppressed by the presence of heterocycles, side-groups and in many non-alternant PAHs. The spectral characteristics of PAHs offer the potential, under suitable circumstances, for remote characterization of the classes of PAH present and in some cases, identification of particular heterocyclic or side-group substituents. (C) 2014 Elsevier Inc. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.icarus.2014.04.033
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000337556400014&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.icarus.2014.04.033
  • ISSN : 0019-1035
  • eISSN : 1090-2643
  • Web of Science ID : WOS:000337556400014

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