Effect of adsorption-catalytic deformation and partial deactivation on the determination of the absolute activity of a liquid phase hydrogenation catalyst
https://doi.org/10.32362/2410-6593-2023-18-4-341-354
Abstract
Objectives. To take into account the change in the number of active sites during the adsorptioncatalytic deformation and deactivation of a catalyst surface by means of a catalytic poison when calculating the turnover frequency (TOF) of a hydrogenation catalyst.
Methods. The activity was determined by a static method, using a titanium reactor having a volume of 400 mL, an experimental temperature controlled using a liquid thermostat with an accuracy of 0.5 K, with a paddle stirrer rotation speed of 3600 rpm and system hydrogen pressure equal to atmospheric. The consumption of hydrogen used to reduce the model compound was taken into account via the volumetric method. The heats of hydrogen adsorption were determined using a reaction calorimeter with an operating mode close to that of a chemical reactor. After measuring the specific surface area using low temperature nitrogen adsorption, the results were processed using Brunauer–Emmett–Teller theory approximations. Deactivation was carried out by introducing dosed amounts of catalytic poison into the system in titration mode.
Results. A kinetic experiment for the reduction of a multiple carbon bond in a sodium maleate molecule using aqueous solutions of sodium hydroxide with additions of monohydric aliphatic alcohols as solvents under conditions of partial deactivation of the catalyst was carried out. The obtained values of heats of hydrogen adsorption on skeletal nickel in the course of the experiment are given. The described approach is used to calculate TOF values taking into account changes in the number of active surface sites during the course of a catalytic reaction and upon the introduction of a deactivating agent. A refined equation for the correct calculation of TOF is proposed along with its mathematical justification. The results of TOF calculations under various assumptions for a number of catalytic systems are shown.
Conclusions. When calculating absolute activity values, a change in the number of active sites has a significant effect on the obtained values. The physical meaning of a number of constants in the proposed equation relates the activity of the catalyst to the distribution of hydrogen on its surface in terms of heats of adsorption.
Keywords
About the Authors
A. V. AfineevskiiRussian Federation
Andrey V. Afineevskii, Cand. Sci. (Chem.), Senior Researcher, Research Laboratory for Synthesis, Research and Testing of Catalytic and Adsorption Systems for Hydrocarbon Processing
7, pr. Sheremetevskii, Ivanovo, 153000
D. A. Prozorov
Russian Federation
Dmitry A. Prozorov, Dr. Sci. (Chem.), Senior Researcher, Research Laboratory for Synthesis, Research and Testing
of Catalytic and Adsorption Systems for Hydrocarbon Processing
7, pr. Sheremetevskii, Ivanovo, 153000
T. Yu. Osadchaya
Russian Federation
Tatyana Yu. Osadchaya, Cand. Sci. (Chem.), Researcher, Research Laboratory for Synthesis, Research and Testing
of Catalytic and Adsorption Systems for Hydrocarbon Processing
7, pr. Sheremetevskii, Ivanovo, 153000
N. E. Gordina
Russian Federation
Natalya E. Gordina, Rector
7, pr. Sheremetevskii, Ivanovo, 153000
References
1. Syrkin Ya.K. On the question of the rate of chemical reactions. Zhurnal Russkogo fiziko-khimicheskogo obshchestva. Chast’ khimicheskaya = J. Rus. Phys.-Chem. Society. Part Chem. 1926;58(8):1101–1128 (in Russ.).
2. Syrkin Ya.K. Types of active complexes and their role in homogeneous catalysis. In: Problemy kinetiki i kataliza (Problems of Kinetics and Catalysis). Institute of Physical Chemistry. Moscow: USSR Academy of Sciences Publishing House; 1960. P. 225–239 (in Russ.).
3. Syrkin Ya.K. Catalysis. Zhurnal khimicheskoi promyshlennosti = Сhem. Ind. J. 1926;39(13):1034–1039 (in Russ.).
4. Selivanova A.S., Syrkin Ya.K. On the influence of the solvent on the kinetics. Doklady Akademii nauk SSSR = Reports of the Academy of Sciences of the USSR. 1939;23(1):49–53 (in Russ.).
5. Startsev A.N. Sul’fidirovannye katalizatory gidroochistki: sintez, struktura, svoistva (Sulfated Hydrotreating Catalysts: Synthesis, Structure, Properties). Boreskov Institute of Catalysis SB RAS. Novosibirsk: Geo; 2007. 206 p. (in Russ.).
6. Korobov M.V. Programma kursa lektsii po “Fizicheskoi Khimii” (The program of the course of lectures on Physical Chemistry). Faculty of Chemistry, Lomonosov Moscow State University. Moscow; 2016 (in Russ.). https://korobov.chem.msu.ru/uploads/TOF.pdf
7. Harris T.K., Keshwani M.M. Measurement of enzyme activity. Methods Enzymol. 2009;463:57–71. https://doi.org/10.1016/S0076-6879(09)63007-X
8. Kozuch S., Martin J.M.L. “Turning over” definitions in catalytic cycles. ACS Catal. 2012;2(12):2787–2794. https://doi.org/10.1021/cs3005264
9. Kulakova I.I., Lisichkin G.V. Kataliticheskaya khimiya. Chast’ 1. Osnovy kataliza (Catalytic Chemistry. Part 1. Fundamentals of Catalysis). Lomonosov Moscow State University. Moscow; 2014. 112 p. URL: https://www.chem.msu.su/rus/teaching/oil-kadry/kulakova-lisichkin-catalysis-p1-2014.pdf
10. Syrkin Ya. K., Vasiliev V.G. Reaction rate and amount of catalyst. Doklady Akademii nauk SSSR = Reports of the Academy of Sciences of the USSR. 1935;1(7–8):513–517.
11. Hagen J. Industrial Catalysis: A Practical Approach. Wiley‐VCH Verlag GmbH & Co. KgaA; 2015. 522 p. http://doi.org/10.1002/9783527684625
12. Afineevskii A.V., Knyazev A.V., Lukin M.V., Osadchaya T.Yu., Prozorov D.A., Rumyantsev R.N. Kataliticheskie svoistva i dezaktivatsiya skeletnogo nikelya v reaktsiyah zhidkofaznoy gidrogenizatsii (Catalytic properties and deactivation of skeletal nickel in liquid-phase hydrogenation reactions). Knyazev A.V. (Ed.). Ivanovo State University of Chemistry and Technology. Kazan: BUK; 2018. 316 p. (in Russ.). ISBN 978-5-00118-185-9.
13. Afineevskii A.V., Prozorov D.A., Osadchaya T.Yu., Rumyantsev R.N. Gidrirovanie na geterogennykh katalizatorakh (Hydrogenation on heterogeneous catalysts). Kazan: BUK; 2018. 316 p. (in Russ.). ISBN 978-5-00118-597-0
14. Lee M.B., Yang Q.Y., Tang S.L., Ceyer S.T. Activated dissociative chemisorption of CH4 on Ni (111): Observation of a methyl radical and implication for the pressure gap in catalysis. J. Chem. Phys. 1986;85(3):1693–1694. https://doi.org/10.1063/1.451211
15. Coudert F.X., Boutin A., Fuchs A.H., Neimark A.V. Adsorption deformation and structural transitions in metal– organic frameworks: from the unit cell to the crystal. J. Phys. Chem. Lett. 2013;4(19):3198–3205. https://doi.org/10.1021/jz4013849
16. Kubota J., Zaera F. Adsorption geometry of modifiers as key in imparting chirality to platinum catalysts. J. Am. Chem. Soc. 2001;123(44):11115–11116. https://doi.org/10.1021/ja016722n
17. Ma X., Liu Y., Li X., Xu J., Gu G., Xia C. Water: the most effective solvent for liquid-phase hydrodechlorination of chlorophenols over Raney Ni catalyst. Appl. Catal. B: Environmental. 2015;165:351–359. https://doi.org/10.1016/j.apcatb.2014.10.035
18. Sanyal U., Song Y., Singh N., Fulton J.L., Herranz J., Jentys A., Lercher J.A. Structure sensitivity in hydrogenation reactions on Pt/C in aqueous‐phase. ChemCatChem. 2019;11(1):575–582. https://doi.org/10.1002/cctc.201801344
19. Prozorov D.A., Afineevskii A.V., Smirnov D.V., Nikitin K.A. Adsorption deformation during liquid-phase hydro-genation of unsaturated carbon bonds over bulk and supported nickel catalysts. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Technol. = ChemChemTech. 2022;65(1):66–75 (in Russ.). https://doi.org/10.6060/ivkkt.20226501.6426
20. Afineevskii A.V., Prozorov D.A., Osadchaya T.Y., Nikitin K.A., Knyazev A.V. The Influence of Adsorption Processes on Structural and Catalytic Properties of Nickel. Prot. Met. Phys. Chem. Surf. 2021;57:277–282. https://doi.org/10.1134/S2070205121020027 [Original Russian Text: Afineevskii A.V., Prozorov D.A., Osadchaya T.Y., Nikitin K.A., Knyazev A.V. The Influence of Adsorption Processes on Structural and Catalytic Properties of Nickel. Fizikokhimiya Poverkhnosti i Zashchita Materialov. 2021;57(2):160–165 (in Russ.). https://doi.org/10.31857/S0044185621020029 ]
21. Afineevskii A.V., Prozorov D.A., Knyazev A.V., Osadchaya T.Y. Correlation of Distribution Functions of Hydrogen Adsorption and Disodium Maleate Hydrogenation Activity for the Nickel Catalyst in Aqueous Solution. Chemistry Select. 2020;5(3):1007–1012. https://doi.org/10.1002/slct.201903608
22. Li J., Qian L. P., Hu L.Y., Yue B. Low-temperature hydrogenation of maleic anhydride to succinic anhydride and γ-butyrolactone over pseudo-boehmite derived alumina supported metal (metal = Cu, Co and Ni) catalysts. Chin. Chem. Lett. 2016;27(7):1004–1008. http://doi.org/10.1016/j.cclet.2016.03.021
23. Feng Y., Yin H., Wang A., Xie T., Jiang T. Selective hydrogenation of maleic anhydride to succinic anhydride catalyzed by metallic nickel catalysts. Appl. Catal. A: General. 2012;425–426:205–212. http://doi.org/10.1016/j.apcata.2012.03.023
24. Milone C., Crisafulli C., Ingoglia R., Schipilliti L., Galvagno S. A comparative study on the selective hydrogenation of α,β unsaturated aldehyde and ketone to unsaturated alcohols on Au supported catalysts. Catal. Today. 2007;122(3–4):341–351. https://doi.org/10.1016/j.cattod.2007.01.011
25. Klabunovskii E. I., Godunova L.F., Maslova L.K. The catalytic hydrogenation of (+)-carvone on palladium and platinum catalysts. Russ. Chem. Bull. 1972;21(5):1020–1024. https://doi.org/10.1007/BF00853760 [Translated from: Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya. 1972;(5):1063–1068 (in Russ.).]
26. Mélendrez R., Del Angel G., Bertin V., Valenzuela M.A., Barbier J. Selective hydrogenation of carvone and o-xylene on Pd–Cu catalysts prepared by surface redox reaction. J. Mol. Catal. A: Chemical. 2000;157(1):143–149. https://doi.org/10.1016/S1381-1169(99)00426-4
27. Gomez R., Arredondo J., Rosas N., Del Angel G. Selective Carvone Hydrogenation on Rh Supported Catalysts. Studies in Surface Science and Catalysis. 1991;59:185–191. https://doi.org/10.1016/S0167-2991(08)61120-9
28. Bertero N.M., Trasarti A.F., Apesteguía C.R., Marchi A. Solvent effect in the liquid-phase hydrogenation of acetophenone over Ni/SiO2 : A comprehensive study of the phenomenon. J. Appl. Catal. A: General. 2011;394(1):228–238. https://doi.org/10.1016/j.apcata.2011.01.003
29. Carey F.A., Sundberg R.J. Electrophilic Additions to Carbon-Carbon Multiple Bonds. In: Advanced Organic Chemistry: Part B: Reactions and Synthesis. Boston, MA: Springer; 1990. P. 167–218. https://doi.org/10.1007/978-1-4613-9797-7_4
30. Gilbert L., Mercier C. Solvent effects in Heterogeneous Catalysis: Application to the synthesis of Fine Chemicals. Studies in Surface Science and Catalysis. 1993;78:51–66. https://doi.org/10.1016/S0167-2991(08)63303-0
31. Ishmuratov G.Y., Yakovleva M.P., Valeeva E.F., Vydrina V.A., Tolstikov G.A. Monoterpene ketones in the synthesis of optically active insect pheromones. Russ. J. Bioorg. Chem. 2012;38(7):667–688. https://doi.org/10.1134/S1068162012070084
32. Battino R. The Ostwald coefficient of gas solubility. Fluid Phase Equilibria. 1984;15(3):231–240. https://doi.org/10.1016/0378-3812(84)87009-0
33. Zakumbaeva G.D. Vzaimodeistvie organicheskikh soedinenii s poverhnost’yu metallov VIII gruppy (Interaction of Organic Compounds with the Surface of Group VIII Metals). Alma-Ata: Nauka; 1978. Р. 6–229 (in Russ.).
Supplementary files
|
1. Influence of the amount of introduced catalytic poison on the specific surface area of the catalyst | |
Subject | ||
Type | Исследовательские инструменты | |
View
(165KB)
|
Indexing metadata ▾ |
- A kinetic experiment for the reduction of a multiple carbon bond in a sodium maleate molecule using aqueous solutions of sodium hydroxide with additions of monohydric aliphatic alcohols as solvents under conditions of partial deactivation of the catalyst was carried out.
- The obtained values of heats of hydrogen adsorption on skeletal nickel in the course of the experiment are given.
- The described approach is used to calculate turnover frequency (TOF) values taking into account changes in the number of active surface sites during the course of a catalytic reaction and upon the introduction of a deactivating agent.
- A refined equation for the correct calculation of TOF is proposed along with its mathematical justification.
Review
For citations:
Afineevskii A.V., Prozorov D.A., Osadchaya T.Yu., Gordina N.E. Effect of adsorption-catalytic deformation and partial deactivation on the determination of the absolute activity of a liquid phase hydrogenation catalyst. Fine Chemical Technologies. 2023;18(4):341-354. https://doi.org/10.32362/2410-6593-2023-18-4-341-354