Proceedings of the International Conference on Current Problems in Engineering and Applied Sciences (ICCPEAS 2025)

Liquid-Phase Catalytic Oxidation of Alkenyl and Cycloalkenyl Aromatic Hydrocarbons with Hydrogen Peroxide

Authors
T. A. Valiyeva1, *, E. S. Musayeva1, H. M. Alimardanov1, A. A. Mammadov1, N. I. Garibov1
1Y. H. Mamedaliyev Institute of Petrochemical Processes Ministry of Science and Education of the Republic of Azerbaijan, Baku, Azerbaijan
*Corresponding author. Email: tahminavaliyeva1@gmail.com
Corresponding Author
T. A. Valiyeva
Available Online 14 May 2026.
DOI
10.2991/978-94-6239-668-5_28How to use a DOI?
Keywords
Alicyclic unsaturated hydrocarbons; liquid phase; catalytic oxidation; alkenyL aromatic compounds; hydrogen peroxide; multiple bond
Abstract

The reaction of liquid-phase catalytic oxidation of alkenyl and cycloalkeyl aromatic hydrocarbons with hydrogen peroxide with the participation of a heteropoly acid of the Keggin series modified with compounds of rare earth elements was studied. The dependences of the main factors of the oxidation reaction of alkenyl and cycloalkeyl aromatic hydrocarbons on temperature, duration, amount of catalyst, and the molar ratio of hydrocarbon: hydrogen peroxide were determined. For alkenyl aromatic compounds they are as follows: reaction temperature 50–80 ℃, duration 5–8 h, molar ratio of alpha methyl styrene: hydrogen peroxide 1:2, catalyst GdPO4 + H3[PMo12O40] ∙nH2O 1–5% of the mass of the reaction mixture, under these conditions the conversion of alpha methyl styrene is about 55%, for hydrogen peroxide 52%. For alkenyl aromatic compounds they are as follows: reaction temperature 50–80 ℃, duration 5–8 h, molar ratio of alpha methyl styrene: hydrogen peroxide 1:2, catalyst GdPO4 + H3[PMo12O40] ∙nH2O 1–5% of the mass of the reaction mixture, under these conditions the conversion of alpha methyl styrene is about 55%, for hydrogen peroxide 52%. The selectivity for 2-phenylpropanal is 56.8%, for epoxide 30.2%, for diol 11.3%, for phenylacetone 2.0%. Higher results for alkenyl aromatic oxidation with hydrogen peroxide were achieved with the participation of the TbPO4 + H3[PMo12O40] ∙nH2O catalyst, and deeper oxidation of the diol to alpha oxyketone isomers was also achieved. The double bond in 1.2-norbornene compounds, as well as in those with the cyclohexenyl derivative, is quite strained and reacts rapidly with the addition of an oxygen group. At temperatures of 50–700 ℃, the glycol yield reaches 68–70%.

Copyright
© 2026 The Author(s)
Open Access
Open Access This chapter is licensed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.

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Volume Title
Proceedings of the International Conference on Current Problems in Engineering and Applied Sciences (ICCPEAS 2025)
Series
Advances in Engineering Research
Publication Date
14 May 2026
ISBN
978-94-6239-668-5
ISSN
2352-5401
DOI
10.2991/978-94-6239-668-5_28How to use a DOI?
Copyright
© 2026 The Author(s)
Open Access
Open Access This chapter is licensed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.

Cite this article

TY  - CONF
AU  - T. A. Valiyeva
AU  - E. S. Musayeva
AU  - H. M. Alimardanov
AU  - A. A. Mammadov
AU  - N. I. Garibov
PY  - 2026
DA  - 2026/05/14
TI  - Liquid-Phase Catalytic Oxidation of Alkenyl and Cycloalkenyl Aromatic Hydrocarbons with Hydrogen Peroxide
BT  - Proceedings of the International Conference on Current Problems in Engineering and Applied Sciences (ICCPEAS 2025)
PB  - Atlantis Press
SP  - 257
EP  - 263
SN  - 2352-5401
UR  - https://doi.org/10.2991/978-94-6239-668-5_28
DO  - 10.2991/978-94-6239-668-5_28
ID  - Valiyeva2026
ER  -