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Laboratory astrochemistry: catalytic reactions of organic molecules over olivine-type silicates and SiC

Published online by Cambridge University Press:  04 September 2018

Qian Li
Affiliation:
Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China. email: hrsccsc@hku.hk
B. S. Liu
Affiliation:
Department of Chemistry, Tianjin University, Tianjin 300072, China.
P. J. Sarre
Affiliation:
School of Chemistry, The University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom
A. S-C. Cheung
Affiliation:
Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China. email: hrsccsc@hku.hk
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Abstract

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A series of catalytic reactions has been performed in our laboratory using olivine-type silicates (OTS) and SiC as catalysts for the conversion of carbon-containing molecules (such as acetylene, CO and methanol) to small organic molecules (C2H4, C3H3, CH3O) and also polycyclic aromatic hydrocarbons (PAHs). Experimentally, small-to-medium-sized gas-phase compounds such as PAHs, reaction intermediates and hydrocarbon compounds were detected in situ using the time-of-light mass-spectrometry technique. Solid deposition on the catalyst surface was examined by high-resolution transmission electron microscopy and thermo-gravimetric analysis techniques. Our laboratory results show that the conversion of acetylene to PAHs, the CO disproportionation reaction for producing CO2 and carbon deposition (graphitic and carbon nanostructures), and also the transformation of methanol to hydrocarbon compounds can easily be achieved with OTS as a catalyst. Furthermore, the conversion of acetylene to PAHs could also be achieved by SiC as the catalyst. It is proposed that these catalytic reactions mimic similar chemical processes in circumstellar envelopes (CSEs).

Type
Contributed Papers
Copyright
Copyright © International Astronomical Union 2018 

References

Dai, H., Rinzler, G., Nikolaev, P., Thess, A., Colbert, D. T., & Smalley, R. E., 1996, Chem. Phys. Lett., 260, 471Google Scholar
Draine, B. T. 2003 ARAA, 41, 241Google Scholar
Ertl, G., Knozinger, H., Schuth, F., & Weitkamp, J. 2008, Handbook of Hetero. Cat., Vol. 4Google Scholar
Ferrante, R. F., Moore, M. H., Nuth, J. A., & Smith, T., 2000, Icarus, 145, 297Google Scholar
Henning, T., 2010, ARAA, 48, 21Google Scholar
Herbst, E., Chang, Q., & Cuppen, H. M., 2005, J. Phys. Conf. Sers., 6, 18Google Scholar
Kress, M. E. & Tielens, A. G. G. M., 2001, Meteor. & Planet. Sci., 36, 75Google Scholar
Merino, P., Svec, M., Martinez, J. I., Jelinek, P., Lacovig, P., Dalmiglio, M., Lizzit, S., Soukiassian, P., Cernicharo, J., & Martin-Gago, J. A. 2014, Nat. Comm., 5, 3054Google Scholar
Öberg, K. I., 2016, Chem. Rev., 116, 9631Google Scholar
Olah, G. A., Mathew, T., Prakash, G. K. S., & Rasul, G., 2016, J. Am. Chem. Soc., 138, 1717Google Scholar
Pirronello, V., Biham, O., Liu, C., Shen, L., & Vidali, G., 1997, ApJ, 483, L131Google Scholar
Zhao, T. Q., Li, Q., Liu, B. S., Sarre, P. J., & Cheung, A. S.-C. 2016, PCCP, 18, 3489Google Scholar
Ziurys, L. M. 2016, Proc. Natl. Acad. Sci. U S A, 103, 12274Google Scholar