ISOMERIZATION OF 1-BUTENE TO 2-BUTENES
931
Synth. Catal., 2007, vol. 349, pp. 1604–1608.
24. Rosynek, M.P. and Fox, J.S., J. Catal., 1977, vol. 49,
pp. 285–293.
8. Panov, G.I., Dubkov, K.A., and Kharitonov, A.S., Modern
Heterogeneous Oxidation Catalysis: Design, Reactions,
and Characterization, Mizuno, N., Ed., Weinheim:
Wiley–VCH, 2009, pp. 217–252.
25. Goldwasser, J. and Hall, W.K., J. Catal., 1980, vol. 63,
pp. 520–522.
26. Chang, C.C., Conner, W.C., and Kokes, R.J., J. Phys.
Chem., 1973, vol. 77, no. 16, pp. 1957–1964.
9. Newman, S.G., Lee, K., Cai, J., Yang, L., Green, W.H.,
and Jensen, K., Ind. Eng. Chem. Res., 2015, vol. 54,
pp. 4166–4173.
27. Tsuchiya, S., Kawasaki, S., Mikami, M., and Imamura, H.,
Zeolites, 1987, vol. 7, pp. 4–6.
10. Dubkov, K.A., Panov, G.I., and Parmon, V.N., Russ.
Chem. Rev., 2017, vol. 86, no. 6, pp. 510–529.
28. Tsuchiya, S. and Ito, S., Zeolites, 1983, vol. 3, pp. 193–
194.
29. Harrison, I.D., Leach, H.F., and Whan, D.A., Zeolites,
11. BASF Starts up a New Production Facility for
Intermediates (BASF News Release, Dec. 1, 2009). http://
A-New-Production-Facility-For-0001. Cited Sept. 21,
2018.
1987, vol. 7, pp. 21–27.
30. Tsuji, H., Yagi, F., and Hattori, H., Chem. Lett., 1991,
vol. 20, no. 11, pp. 1881–1884.
31. Li, J.H. and Davis, R.J., Appl. Catal. A: General, 2003,
12. Semikolenov, S.V., Dubkov, K.A., Starokon, E.V.,
Babushkin, D.E., and Panov, G.I., Russ. Chem. Bull.,
2005, vol. 54, no. 4, pp. 948–956.
vol. 239, pp. 59–70.
32. Slomkiewicz, P.M., Appl. Catal. A: General, 2006,
vol. 301, no. 2, pp. 232–240.
13. Sheldon, R.A. and Kochi, J.K., Metal-Catalyzed
Oxidations of Organic Compounds, London: Academic,
1981.
33. Slomkiewicz, P.M., React. Funct. Polym., 1997, vol. 33,
nos. 2–3, pp. 299–304.
34. Chesnokov, V.V., Bedilo, A.F., Heroux, D.S.,
Mishakov, I.V., and Klabunde, K.J., J. Catal., 2003,
vol. 218, pp. 438–446.
14. Hudlicky, M., Oxidation in Organic Chemistry,
Washington, DC: ACS, 1990.
15. Kharitonov, A.S., Ivanov, D.P., Parfenov, M.V.,
Piryutko, L.V., Semikolenov, S.V., Dubkov, K.A.,
Pereima, V.Y., Noskov, A.S., Kondrashev, D.O.,
Kleymenov, A.V., Vedernikov, O.S., Kuznetsov, S.E.,
Galkin, V.V., and Abrashenkov, P.A., Catal. Ind., 2017,
vol. 9, no. 3, pp. 204–211.
35. Simon, M., Sui, S., and O’Young, C.L., J. Catal., 1994,
vol. 147, pp. 484–493.
36. Wichterlova, B., Zilkova, N., Uvarova, E., Cejka, J.,
Sarv, P., Paganini, C., and Lercher, J.A., Appl. Catal. A:
General, 1999, vol. 182, pp. 297–308.
37. Hensen, E.J.M. and van Veen, J.A.R., Catal. Today, 2003,
16. Patent RU 2570818 С1, Publ. 2015.
vol. 86, pp. 87–109.
17. Stull, D.R., Westrum, E.F., and Sinke, G.C., The Chemical
Thermodynamics of Organic Compounds, New York:
Wiley, 1969.
38. Qiao, Z.A. and Huo, Q.-S., Modern Inorganic Synthetic
Chemistry, Xu, R. and Xu, Y., Eds., Amsterdam: Elsevier,
2017, 2nd ed., pp. 389–428.
18. Dent, A.L. and Kokes, R.J., J. Phys. Chem., 1970, vol. 76,
39. Weeks, T.J. and Bolton, A.P., J. Chem. Soc., Faraday
Trans. 1, 1974, vol. 70, pp. 1676–1684.
no. 4, pp. 487–491.
19. Meyer, E.F. and Stroz, D.G., J. Am. Chem. Soc., 1972,
40. Jacobs, P.A., Declerck, L.J., Vandamme, L.J., and
Uytterhoeven, J.B., J. Chem. Soc., Faraday Trans. 1,
1975, vol. 71, pp. 1545–1556.
vol. 94, no. 18, pp. 6344–6347.
20. Matsuda, T., Tanabe, J., Hayashi, N., Sasa-
ki, Y., Miura, H., and Sugiyama, K., Bull. Chem. Soc.
Jpn., 1982, vol. 55, pp. 22–31.
41. Haag, W.O., Lago, R.M., and Weisz, P.B., Nature, 1984,
vol. 309, pp. 589–591.
42. Woolery, G.L., Kuehl, G.H., Timken, H.C., Chester,A.W.,
21. Baird, M.J. and Lunsford, J.H., J. Catal., 1972, vol. 26,
and Vartuli, J.C., Zeolites, 1997, vol. 19, pp. 288–296.
pp. 440–450.
43. Costa, C., Dzikh, I.P., Lopes, J.M., Lemos, F., and
Ribeiro, F.R., J. Mol. Catal. A: Chemical, 2000, vol. 154,
pp. 193–201.
22. Gerberich, H.R. and Hall, W.K., J. Catal., 1966, vol. 5,
pp. 99–110.
23. Rosynek, M.P., Fox, J.S., and Jensen, J.L., J. Catal.,
44. Benito, P.-L., Gayubo, A.G., Aguayo, A.T., Olazar, M.,
1981, vol. 71, pp. 64–77.
RUSSIAN JOURNAL OF APPLIED CHEMISTRY Vol. 92 No. 7 2019