NAPHTHALENE HYDROGENATION OVER CATALYSTS
1219
8
. S. Eijsbouts, V. J. H. de Beer, and R. Prins, J. Catal. 109
Naphthalene conversion
Selectivity for tetralin
(
1), 217 (1988).
. M. J. Ledoux and B. Djellouli, J. Catal. 115 (2), 580
1989).
%
9
100
(
1
0. www.cmmarket.ru/markets/rtworld.htm. Cited Janu-
80
60
40
20
0
ary 12, 2017.
11. M. Lacroix, N. Boutarfa, C. Guillard, M. Vrinat, and
M. Breysse, J. Catal. 120 (2), 473 (1989).
12. J. Quartararo, S. Mignard, and S. Kasztelan, J. Catal.
1
92 (2), 307 (2000).
13. A. Infantes-Molina, A. Romero-Perez, D. Eliche-
Quesada, J. Merida-Robles, A. Jimenez-Lopez, and
E. Rodriguez-Castellon, Transition Metal Sulfide Cata-
lysts for Petroleum Upgrading – Hydrodesulfurization
Reactions (InTech, 2012), 248 p.
P1–Ni P1–Ni P1–Ni P1–Ni P1–Ni
14. A. Romero-Perez, A. Infantes-Molina, E. Rodriguez-
in IL
in IL
in IL
in IL
Castellon, and A. Jimenez-Lopez, Appl. Catal., B 97
(1 cycle) (2 cycle) (3 cycle) (4 cycle)
(1–2), 257 (2010).
1
5. A. Romero-Perez, A. Infantes-Molina, A. Jimenez-
Fig. 6. Comparison of the activities of catalysts formed
from precursor P1–Ni and precursor in ionic liquid.
Lopez, JalilE. Roca, K. Sapag, and E. Rodriguez-Cas-
tellon, Catal. Today 187, 88 (2012).
1
6. S. Zhang, D. Liu, W. Deng, and G. Que, Energy Fuels
2
1 (6), 3057 (2007).
Thus, we showed that the degree of conversion of
naphthalene and the selectivity of hydrogenation for 17. M. T. Nguyen, N. T. Nguyen, J. Cho, C. Park, S. Park,
J. Jung, and C. W. Lee, J. Ind. Eng. Chem. 43, 1 (2016).
Ni/[BMPip]Ru S precursors depend on the method 18. M. I. Onishchenko, A. B. Kulikov, and A. L. Maksi-
the catalysts formed in situ from [BMPip]Ru S and
x
y
x
y
mov, Pet. Chem. 57 (14), 1225 (2017).
were synthesized in situ in a thermally stable ionic liq- 19. E. M. Zakharyan, M. I. Onishchenko, and A. L. Mak-
simov, Pet. Chem. 58 (1), 22 (2018).
reaction of naphthalene hydrogenation without any 20. I. A. Sizova and A. L. Maksimov, Pet. Chem. 57 (7),
595 (2017).
of preparing precursors. Sulfide ruthenium catalysts
uid, and it was shown that they can be reused in the
loss in activity.
2
1. I. A. Sizova, S. I. Serdyukov, and A. L. Maksimov, Pet.
Chem. 55 (6), 470 (2015).
ACKNOWLEDGMENTS
2
2. E. A. Karakhanov, A. L. Maksimov, E. A. Runova, Y.
S. Kardasheva, M. F. Terenina, T. S. Buchneva, and A.
Ya. Guchkova, Macromol. Symp. 204 (2003).
This work, supported by the Federal Agency for
Scientific Organizations of Russia, was performed
within the scope of State Task for the Topchiev Insti- 23. D. N. Gorbunov, A. V. Volkov, Yu. S. Kardasheva, A.
tute of Petrochemical Synthesis, Russian Academy of
Sciences.
L. Maksimov, and E. A. Karakhanov, Pet. Chem. 55
8), 587 (2015).
(
2
2
2
4. P. J. Dyson, D. J. Ellis, and T. Welton, Platinum Metals
Rev. 42 (4), 135 (1998).
REFERENCES
5. E. A. Karakhanov and A. L. Maksimov, Ross. Khim.
1
2
3
4
. A. Stanislaus, A. Marafi, and M. S. Rana, Catal. Today
53 (2010).
. R. R. Aliev, Petroleum Refining Catalysts and Processes
Khimiya, Moscow, 2010) [in Russian].
. Z. L. Solodova and A. R. Nurmukhametova, Vestn.
Tekhnol. Univ. 20 (10), 53 (2017).
Zh. 52 (4), 125 (2009).
1
6. L. A. Aslanov, M. A. Zakharov, and N. L. Abramy-
cheva, Ionic Liquids in the Series of Solvents (Mosk.
Univ., Moscow, 2005) [in Russian].
(
27. A. L. Maksimov, S. N. Kuklin, Yu. S. Kardasheva, and
E. A. Karakhanov, Pet. Chem. 53 (3), 157 (2013).
28. E. A. Karakhanov, A. L. Maksimov, and E. A. Runova,
. M. Fahim, T. Al-Sahhaf, and A. Elkilani, Fundamen-
Russ. Chem. Rev. 74 (1), 97 (2005).
tals of Petroleum Refining (Elsevier Science, 2009), 516
p.
29. T. Welton, Coord. Chem. Rev. 248 (21-24), 2459
(2004).
5
. A. L. Maximov, I. A. Sizova, and S. N. Khadzhiev,
Pure Appl. Chem. 89 (8), 1145 (2017).
30. L. M. Kustov, T. V. Vasina, and V. A. Ksenofontov,
Russ. Chem. J. 43 (5), 45 (2004).
6
. H. Toulhoat and P. Raybaud, Catalysis by Transition
Metal Sulphides: From Molecular Theory to Industrial 31. A. Taubert and Z. Li, Dalton Trans., No. 7, 723 (2007).
Application (Editions Technips, 2013), 787 p.
3
2. C. Hardacre and V. Parvulescu, Catalysis in Ionic Liq-
uids: From Catalyst Synthesis to Application (Royal Soci-
ety of Chemistry, 2014), 620 p.
7
. T. A. Pecoraro and R. R. Chianelli, J. Catal. 67 (2), 430
(1981).
PETROLEUM CHEMISTRY Vol. 58 No. 14 2018