The process of joint dehydration of high-boiling components (HBC) formed at various units of the dehydration process of methylphenyl carbinol (MPC) in the joint production of styrene and propylene oxide, and the MFC fraction in the presence of sulfamic acid was studied. It was shown that joint dehydration of HBC and the MFC fraction in the presence of sulfamic acid leads to an increase in the styrene content in the decomposition products (60.29 %) compared to the dehydration of the MFC fraction (52.19 %). In this case, complete conversion of MFC and HBC is not achieved. By introducing live steam into the bottom part of the dehydrator, a styrene fraction containing at least 95.55 % by weight of the main substance was obtained from a mixture of the methylphenylcarbinol fraction and high-boiling components. The mixture was dehydrated continuously in a specially designed laboratory unit with separate collection of low-boiling and high-boiling reaction products. Qualitative and quantitative analysis of dehydration products was performed by chromatographic-mass spectrometry on Agilent 5975 Series MSDs. Mass spectra were obtained at an ionizing ion energy of 69 eV. It was found that introducing live steam into the dehydration reactor allows achieving high conversion of methylphenylcarbinol and high-boiling aromatic ethers and selectivity of styrene formation due to its immediate separation from the reaction zone. The mass ratio of water vapor: batch = 64:100 was found, ensuring maximum styrene extraction.
STYRENE, METHYLPHENYL CARBINOL, HIGH-BOILING COMPONENTS, HIGH-BOILING AROMATIC ETHERS, DEHYDRATION, SULFAMIC ACID, LIQUID-PHASE PROCESS
1. Talanyuk V., Shadrin A., Yurzhenko M. Bull. Taras Shevchenko Natl. Univ. Kyiv Phys. Math. 2, 98-103 (2019). DOI:https://doi.org/10.17721/1812-5409.2019/2.13.
2. Shell Internationale Research Maatschappij BV. Pat. 3365314 B1 EP. (2018).
3. Pat. 2721772 Russian Federation, IPC B01J 20/08, B01J 21/04, B01J 23/78, C07C 1/24, C07C 15/46. [Title of the invention] / NPO “EVROCHIM” LLC; Applicant and patent holder: LLC NPO “EUROCHEM”. – No. 2019139330; filed Dec. 2, 2019; published May 22, 2020, Bulletin No. 15.
4. Sitmuratov T.S., Petukhova L.A., Petukhov A.A. Butlerov'smessages. 60(12), 104-109 (2019). DOI:https://doi.org/10.37952/ROI-jbc-01/19-60-12-104. EDN: https://elibrary.ru/ZELKCB
5. PJSC "Nizhnekamskneftekhim" website. URL: https://www.sibur.ru/nknh.ru (2026).
6. Lychkin I.P., Petykhin Y.M., Filimonova O.N. Neftepererabotka i neftekhimiya. 11, 29-31 (1995).
7. Vora B.V. Trans Indian Natl. Acad. Eng. 8, 201-219 (2023). DOI:https://doi.org/10.1007/s41403-023-00401-2. EDN: https://elibrary.ru/UMWVOR
8. Nabiullin I.R. et al. Catal. Ind. 14(4), 376-384 (2022). DOI: https://doi.org/10.1134/S2070050422040080
9. Karalin E.A. et al. Neftekhimiya. 6, 455-457 (2001). EDN: https://elibrary.ru/PQGTKT
10. Lange J.P., Otten V. J. Catal. 238(1), 6-12 (2006). DOI: https://doi.org/10.1016/j.jcat.2005.11.033; EDN: https://elibrary.ru/KEWUBH
11. Boretskaya A. et al. Research Square [Preprint]. (2022). DOI:https://doi.org/10.21203/rs.3.rs-1800475/v1.
12. Karalin E.A., Kharlampidi K.E., Busygin V.M., Batyrshin N.N., Cherkasova E.I. Tez. dokl. V Russian Conf. "Scientific foundations of catalyst preparation and technology". 137-139 (2004).
13. Filimonova O.N. Uspekhi sovremennogo estestvoznaniya. 2, 115-117 (2010).
14. Sitmuratov T.S. Razrabotka tekhnologii polucheniya stirola na osnove metilfenilkarbinola i vysokokipyashikh aromaticheskikh efirov: dis. kand. khim. nauk. – Kazan, 2022. 109 s. EDN: https://elibrary.ru/AHTEIO
15. Sitmuratov T.S., Chugunov Y.V., Petukhov A.A. Butlerov'smessages. 65(2), 130-136 (2021). DOI: https://doi.org/10.37952/ROI-jbc-01/21-65-2-130; EDN: https://elibrary.ru/DKSORM
16. Sitmuratov T.S., Petukhova L.A., Bakhtinova I.I., Petukhov A.A. Butlerov's messages. 56(10), 118-122 (2018). EDN: https://elibrary.ru/VQFVGM
17. Petukhov A.A., Vasiliev I.M., Galimzyanov R.M. Pat. 2141933 RF. (1999).
18. Linkova T.S., Dolganov A.V., Zemsky D.N. Herald of Kazan Technological University. 16(12), 211-213 (2013). EDN: https://elibrary.ru/QCWPOP
19. Vuitsik E.I., Dement'ev A.I., Podoplelov E.V. Mod. Technol. Sci. Technol. Progress. 1, 19-20 (2022). DOI:https://doi.org/10.36629/2686-9896-2022-1-19-20.
20. Petukhov A.A., Komarov V.A., Sakhapov G.Z. Pat. 2120934 RF. (1998).
21. Ikeda Y., Sugawara H. Appl. 59-67231 Japan. (1984).
22. Ikeda S. et al. Appl. 55-19247 Japan. (1980).
23. Gupta R., Uslu H., Majumder S. Chem. Eng. Technol. 45, 817-823 (2022). DOIhttps://doi.org/10.1002/ceat.202100577. EDN: https://elibrary.ru/METUDD
24. Hutajulu F.T.M., Vito A.A., Fakhira F., Izzati D.S. J. Chem. Eng. Res. Prog. 2(1), 61-71 (2025). DOI:https://doi.org/10.9767/jcerp.20312. EDN: https://elibrary.ru/XXGYUR
25. Wang R., Zhao Z., Gao P., Chen K., Gan Z., Fu Q., Hou G. J. Phys. Chem. C. 126(22), 10073-10084 (2022). DOI:https://doi.org/10.1021/acs.jpcc.2c03303. EDN: https://elibrary.ru/CUSZED
26. Polovnyak V.K., Fridland S.V. Herald of Kazan Technological University. 4, 17-25 (2009) EDN: https://elibrary.ru/KTZAGJ



