Transformations of ethylene and propylene on molybdenum oxide catalysts deposited on γ-alumina and silica gel
https://doi.org/10.18412/1816-0387-2025-6-31-44
Abstract
The physicochemical properties, the state of the active component, the activity and selectivity of deposited molybdenum-containing catalysts in the processes of ethylene to propylene conversion and propylene metathesis are considered. It is shown that the activity of molybdenum-containing catalysts in the transformations of ethylene and propylene increases with an increase in the number of medium-strength and strong acid centers on their surface. The alumina-based catalyst is active at temperatures of 100-250 °C. At the same time, a silica gel-based catalyst requires temperatures up to 500 °C. The higher activity of the MoO3/γ-Al2O3 catalyst in metathesis reactions is associated with the formation of highly dispersed molybdenum compounds and Brensted acid centers.
About the Authors
T. R. KarpovaRussian Federation
A. V. Lavrenov
Russian Federation
M. A. Moiseenko
Russian Federation
T. I. Gulyaeva
Russian Federation
A. B. Arbuzov
Russian Federation
A. V. Bukhtiyarov
Russian Federation
E. Yu. Gerasimov
Russian Federation
T. S. Glazneva
Russian Federation
References
1. Sadrameli S.M. // Fuel. 2016. V. 173. P. 285 – 297. https://doi.org/10.1016/j.fuel.2016.01.047.
2. Speight J.G. // Refin. Futur. 2011. № 1. P. 315 – 340. https://doi.org/10.1016/B978-0-8155-2041-2.10010-4.
3. Speight J.G. // Heavy Extra-heavy Oil Upgrad. Technol. 2013. P. 39 – 67. https://doi.org/10.1016/B978-0-12-404570-5.00003-X.
4. Третьяков В.Ф., Илолов А.М., Будняк А.Д., Французова Н.А., Рагуткин А.В., Латышков А.А., Никоноров С.И. // НефтеГазоХимия. 2017. № 3. С. 35 – 40.
5. Bao J., Yang G., Yoneyama Y., Tsubaki N. // ACS Catal. 2019. V. 9. P. 3026 – 3053. https://doi.org/10.1021/acscatal.8b03924.
6. Голинский Д.В., Виниченко Н.В., Затолокина Е.В., Пашков В.В., Паукштис Е.А., Гуляева Т.И., Павлюченко П.Е., Кроль О.В., Белый А.С. // Рос. Хим. Ж. 2019. Т. 62. № 1-2. С. 55 – 72. https://doi.org/10.6060/rcj.2018621-2.5
7. Speight J.G. // Handbook of Industrial Hydrocarbon Processes. 2020. P. 55 – 93. https://doi.org/10.1016/B978-0-12-809923-0.00002-3.
8. Vogt E.T.C., Whiting G.T., Chowdhury A.D., Weckhuysen B.M. // Adv. Catal. 2015. V. 58. P. 143 – 314. https://doi.org/10.1016/bs.acat.2015.10.001
9. Matar S., Hatch L.F. Chemistry of petrochemical processes. Houston: Gulf Publishing Company, 1995. 392 p. https://doi.org/10.5860/CHOICE.32-2746.
10. Mol J.C. // J. Mol. Catal. A: Chem. 2004. V. 213. P. 39 − 45. https://doi.org/10.1016/j.molcata.2003.10.049.
11. Mol J.C., van Leeuwen P.W.N.M. Handbook of Heterogeneous Catalysis. Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA, 2008. P. 3240 – 3256. https://doi.org/10.1002/9783527610044.hetcat0164.
12. Патент US 4575575, опубл. 11.03.1986.
13. van Schalkwyk C., Spamer A., Moodley D.J., Dube T., Reynhardt J., Botha J.M. // Appl. Catal. A Gen. 2003. V. 255. P. 121 – 131. https://doi.org/10.1016/S0926-860X(03)00534-9.
14. Fierro J.L.G., Mol J.C. Metal Oxides: Chemistry and Applications. Boca Raton: Taylor & Francis, 2006. P. 517 – 520. https://doi.org/10.1201/9781420028126.
15. Chakrabarti A., Wachs, I.E. // J. Phys. Chem. C. 2019. V. 123. P. 12367 − 12375. https://doi.org/10.1021/acs.jpcc.9b02426.
16. Otroshchenko T., Zhang Q., Kondratenko E.V. // Catal. Let. 2022. V. 152. P. 2366 – 2374. https://doi.org/10.1007/s10562-021-03822-2.
17. Hahn T., Bentrup U., Armbruster M., Kondratenko E.V., Linke D. // ChemCatChem. 2014. V. 6. P. 1664 – 1672. https://doi.org/10.1002/cctc.201400040.
18. Topka P., Balcar H., Rathousky J., Zilkova N., Verpoort F., Cejka J. // Microporous Mesoporous Mater. 2006. V. 96. P. 44 – 54. https://doi.org/10.1016/j.micromeso.2006.06.016.
19. Debecker D.P., Schimmoeller B., Stoyanova M., Poleunis C., Bertrand P., Rodemerck U., Gaigneaux E.M. // J. Catal. 2011. V. 277. P. 154 – 163. https://doi.org/10.1016/j.jcat.2010.11.003.
20. Debecker D.P., Stoyanova M., Rodemerck U., Gaigneaux E.M. // J. Mol. Catal. A. 2011. V. 340. P. 65 – 76. https://doi.org/10.1016/j.molcata.2011.03.011.
21. Debecker D.P., Stoyanova M., Rodemerck U., Lonard A., Su B.-L., Gaigneaux E.M. // Catal. Today. 2011. V. 169. P. 60 – 68. https://doi.org/10.1016/j.cattod.2010.07.026.
22. Nikiforov A.I., Chesnokov E.A., Popov A.G., Ivanova I.I. // J. Catal. 2024. V. 436. P. 115578. https://doi.org/10.1016/j.jcat.2024.115578.
23. Amakawa K., Wrabetz S., Kröhnert J., Tzolova-Müller G., Schlögl R., Trunschke A. // J. Am. Chem. Soc. 2012. V. 134. P. 11462 – 11473. https://doi.org/10.1021/ja3011989.
24. Исмагилов З.Р., Шкрабина Р.А., Корябкина Н.А. // Экология. Серия аналитических обзоров мировой литературы. 1998. Т. 50. С. 1 – 80.
25. Неймарк И.Е., Шейнфайн Р.Ю. Силикагель, его получение, свойства и применение. Киев: Наукова думка, 1973. 202 с.
26. Karpova T., Buluchevskiy E., Lavrenov A., Moiseenko M., Trenikhin M., Arbuzov A., Gulyaeva T., Savelyeva G., Muromtsev I. // Molecular Catalysis. 2021. V. 499. P. 111316:1-9. https://doi.org/10.1016/j.mcat.2020.111316.
27. Scofield J.H. // J. Electron. Spectrosc. Relat. Phenom. 1976. V. 8, P. 129 – 137. https://doi.org/10.1016/0368-2048(76)80015-1.
28. Tian H., Roberts C.A., Wachs I.E. // J. Phys. Chem. C. 2010. V. 114. P. 14110 – 14120. https://doi.org/10.1021/jp103269w.
29. Cui Y., Liu N., Xia Y., Lv J., Zheng S., Xue N., Peng L., Guo X., Ding W. // J. Mol. Catal. A Chem. 2014. V. 394. P. 1 – 9. https://doi.org/10.1016/j.molcata.2014.06.027.
30. Li X., Zhang W., Liu S., Xie S., Zhu X., Bao X., Xu L. // J. Mol. Catal. A Chem. 2009. V. 313. P. 38 – 43. https://doi.org/10.1016/j.molcata.2009.07.020.
31. Morales-Ortuno J.C., Klimova T.E. // Fuel. 2017. V. 198. P. 99 – 109. https://doi.org/10.1016/j.fuel.2017.01.007.
32. Wang B., Ding G., Shang Y., Lv J., H. Wang, Wang E., Li Z., Ma X., Qin S., Sun Q. // Appl. Catal. A Gen. 2012. V. 431 – 432. P. 144 – 150. https://doi.org/10.1016/j.apcata.2012.04.029.
33. Ramanathan A., Wu J.-F., Maheswari R., Hu Y., Subramaniam B. // Microporous Mesoporous Mater. 2017. V. 245. P. 118 – 125. https://doi.org/10.1016/j.micromeso.2017.03.001.
34. Zhang D., Li X., Liu S., Zhu X., Chen F., Xu L. // Appl. Catal. A Gen. 2014. V. 472. P. 92 – 100. https://doi.org/10.1016/j.apcata.2013.12.019.
35. Handzlik J., Ogonowski J., Stoch J., Mikolajczyk M., Michorczyk P. // Appl. Catal. A Gen. 2006. V. 312. № 1 – 2. P. 213 – 219. https://doi.org/10.1016/j.apcata.2006.07.002.
36. Harlin M.E., Backman L.B., Krause A.O.I., Jylha O.J.T. // J. Catal. 1999. V. 183, № 2. P. 300 – 313. https://doi.org/10.1006/jcat.1999.2413.
37. Kerkhof F.P.J.M., Moulijn J.A. // J. Phys. Chem. 1979. V. 83. № 12. P. 1612 – 1619. https://doi.org/10.1021/J100475A011.
38. Grunert W., Stakheev A.Yu., Morke W., Feldhaus R., Anders K., Shpiro E.S., Minachev K.M. // J. Catal. 1992. V. 135. № 1. P. 269 – 286. https://doi.org/10.1016/0021-9517(92)90285-P.
39. Knözinger H., Ratnasamy P. // Catal. Rev. 1978. V. 17. № 1. P. 31 – 70. https://doi.org/10.1080/03602457808080878.
40. Morterra C., Magnacca G. // Catal. Today. 1996. V. 27. № 3 – 4. P. 497 – 532. https://doi.org/10.1016/0920-5861(95)00163-8.
41. Flego C., Carluccio L., Rizzo C., Perego C. // Catal. Commun. 2001. V. 2. № 2. P. 43 – 48. https://doi.org/10.1016/S1566-7367(01)00006-1.
42. Morrow B.A. // Langmuir. 1991. V. 7. № 8. P. 1695 – 1701. https://doi.org/10.1021/la00056a022.
43. Паукштис Е.А. ИК-спектроскопия в гетерогенном кислотно-основном катализе. Новосибирск: Наука, 1992. 253 с.
44. Zecchina A., Platero E.E., Arean C.O. // J. Catal. 1987. V. 107. P. 244 – 247. https://doi.org/10.1016/0021-9517(87)90290-9.
45. Nasser H., Redey A., Yuzhakova T., Toth Z.N., Ollar T. // React. Kinet. Catal. Lett. 2007. V. 92. № 2. P. 329 – 335. https://doi.org/10.1007/s11144-007-5026-3.
46. Bonelli B., Cozzolino M., Tesser R., Di Serio M., Piumetti M., Garrone E., Santacesaria E. // J. Catal. 2007. V. 246. № 2. P. 293 – 300. https://doi.org/10.1016/j.jcat.2006.12.015.
47. Williams C.C., Ekerdt J.G. // J. Phys. Chem. 1993. V. 97. № 26. P. 6843 – 6852. https://doi.org/10.1021/j100128a017.
48. Zaki M.I., Vielhaber B., Knözinger H. // J. Phys. Chem. 1986. V. 90. № 14. P. 3176 – 3183. https://doi.org/10.1021/j100405a026.
49. Лавренов А.В., Островский Н.М., Деманов Ю.К. // Нефтехимия. 2001. Т 41. № 2. С. 144 – 148.
50. Karpova T., Buluchevskiy E., Lavrenov A., Moiseenko M., Trenikhin M., Arbuzov A., Gulyaeva T., Savelyeva G., Muromtsev I. // Mol. Catal. 2021. V. 499. P. 111316:1-9. https://doi.org/10.1016/j.mcat.2020.111316.
51. Карпова Т.Р., Булучевский Е.А., Лавренов А.В., Моисеенко М.А., Арбузов А.Б., Гуляева Т.И., Юрпалов В.Л. // Катализ в промышленности. 2021. Т. 21. № 3. С. 154 – 162. https://doi.org/10.18412/1816-0387-2021-3-154-162.
52. Карпова Т.Р., Лавренов А.В., Моисеенко М.А., Потапенко О.В., Ковеза В.А., Булучевский Е.А., Арбузов А.Б., Василевич А.В. // Катализ в промышленности. 2024. Т. 24. № 6. С. 60 – 69. https://doi.org/10.18412/1816-0387-2024-6-60-69.
53. Karpova T.R., Stepanova L.N., Moiseenko M.A., Lavrenov A.V., Arbuzov A.B., Buluchevskiy E.A., Bukhtiyarov A.V., Glazneva T.S., Gerasimov E.Y. // Appl. Catal. A Gen. 2023. V. 650. P. 119012:1-8. https://doi.org/10.1016/j.apcata.2022.119012.
Review
For citations:
Karpova T.R., Lavrenov A.V., Moiseenko M.A., Gulyaeva T.I., Arbuzov A.B., Bukhtiyarov A.V., Gerasimov E.Yu., Glazneva T.S. Transformations of ethylene and propylene on molybdenum oxide catalysts deposited on γ-alumina and silica gel. Kataliz v promyshlennosti. 2025;25(6):31-44. (In Russ.) https://doi.org/10.18412/1816-0387-2025-6-31-44
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