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Kinetic Study of Propylene Hydrogenation over Pt/Al2O3 by Parahydrogen-Induced Polarization Full article

Journal Applied Magnetic Resonance
ISSN: 0937-9347 , E-ISSN: 1613-7507
Output data Year: 2013, Volume: 44, Number: 1-2, Pages: 279-288 Pages count : 10 DOI: 10.1007/s00723-012-0400-3
Tags Hydrogenation; Kinetic theory; Polarization; Propylene
Authors Salnikov Oleg G. 1,2 , Kovtunov Kirill V. 1,2 , Barskiy Danila A. 1,2 , Bukhtiyarov Valery I. 3 , Kaptein Robert 2,4 , Koptyug Igor V. 1,2
Affiliations
1 International Tomography Center, Siberian Branch, Russian Academy of Sciences, Institutskaya St. 3A, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova St. 2, Novosibirsk 630090, Russia
3 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, 5 Acad. Lavrentiev Pr., Novosibirsk 630090, Russia
4 Bijvoet Center, University of Utrecht, Padualaan 8, 3584 CH Utrecht, The Netherlands

Funding (9)

1 Russian Foundation for Basic Research 11-03-93995
2 Russian Foundation for Basic Research 12-03-00403
3 Siberian Branch of the Russian Academy of Sciences 57
4 Siberian Branch of the Russian Academy of Sciences 60
5 Siberian Branch of the Russian Academy of Sciences 61
6 Siberian Branch of the Russian Academy of Sciences 122
7 Президиум РАН 5.1.1
8 Government of the Russian Federation 11.G34.31.0045
9 Council for Grants of the President of the Russian Federation НШ-2429.2012.3

Abstract: Parahydrogen-induced polarization has been successfully used for a kinetic study of propylene hydrogenation over a Pt/Al2O3 catalyst. It was shown that the reaction orders with respect to hydrogen are different for the pairwise and the non-pairwise hydrogen addition and are equal to 0.7 and 0.1, respectively. This observation of different reaction orders confirms the coexistence of different types of active sites which are responsible for the overall and the pairwise hydrogen addition to the propylene C=C double bond. Moreover, 0.7 reaction order with respect to H2 for pairwise hydrogen addition indicates that the contribution of pairwise addition depends on the concentration of molecular hydrogen. Therefore, this observation can be developed into a practical tool for producing fluids with highly polarized nuclear spins by changing the hydrogen concentration.
Cite: Salnikov O.G. , Kovtunov K.V. , Barskiy D.A. , Bukhtiyarov V.I. , Kaptein R. , Koptyug I.V.
Kinetic Study of Propylene Hydrogenation over Pt/Al2O3 by Parahydrogen-Induced Polarization
Applied Magnetic Resonance. 2013. V.44. N1-2. P.279-288. DOI: 10.1007/s00723-012-0400-3 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jul 20, 2012
Published online: Oct 7, 2012
Published print: Feb 1, 2013
Identifiers:
Web of science: WOS:000313796500024
Scopus: 2-s2.0-84872654355
Elibrary: 20420449
Chemical Abstracts: 2013:144029
Chemical Abstracts (print): 159:196640
OpenAlex: W2467693202
Citing:
DB Citing
Web of science 15
Scopus 18
Elibrary 18
OpenAlex 18
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