Preview

Proceedings of Universities. Applied Chemistry and Biotechnology

Advanced search

Gelation in the aqueous solutions of oxyethylated nonylphenols

https://doi.org/10.21285/achb.965

EDN: UTPISA

Abstract

The study was aimed at ascertaining gelation conditions for the systems water – oxyethylated nonylphenol and water – oxyethylated nonylphenol – salting agent. The work involved analyzing scientific and technical literature on the use of surfactants in extraction processes. Systems containing nonionic surfactants are shown to be promising extraction systems. The effect that the concentration of nonionic surfactants and temperature can have on gelation in aqueous solutions is examined. The problem of using oxyethylated nonylphenols in gel extraction is considered. The phase diagrams of the systems water – neonol AF 9-6 and water – neonol AF 9-6 – sodium sulfate were constructed using the visual polythermal method. Gelation conditions were ascertained for the systems water – neonol AF 9-6 and water – neonol AF 9-6 – sodium sulfate. For the gel to form in the system water – oxyethylated nonylphenol (neonol AF 9-6), the concentration of the surfactant must exceed 25 wt%. For achieving gelation at lower concentrations of neonol AF 9-6, it is necessary to introduce a salting agent (sodium sulfate). The phase diagrams of the systems water – oxyethylated nonylphenol – sodium sulfate were constructed within the temperature range of 20–65 °C. The gel structure was found to form at a 3:1 weight ratio of oxyethylated nonylphenol to sodium sulfate. It is shown that for gelation, the minimum concentrations of neonol AF 9-6 and sodium sulfate are 15 and 5 wt%, respectively. An increase in the concentrations of neonol AF 9-6 and sodium sulfate to 24 and 8 wt%, respectively, leads to a decrease in the gelation temperature to 46 °C.

About the Authors

V. I. Zholnerkevich
Belarusian State Technological University
Belarus

Veronika I. Zholnerkevich, Graduate Student

13a, Sverdlov St., Minsk, 220006



A. O. Shrubok
Belarusian State Technological University
Belarus

Alexandra O. Shrubok, Cand. Sci. (Engineering), Associate Professor

13a, Sverdlov St., Minsk, 220006



References

1. Lesnov A.E., Denisova S.A. Surfactant gel extraction. Bulletin of Perm University. Chemistry. 2014;1:79-92. (In Russian). EDN: SPWJOL.

2. Mouronte N., Álvarez M.S., Deive F.J., Rodríguez A. Combining biodegradable surfactants and potassium inorganic salts for efficiently removing polycyclic aromatic hydrocarbons from aqueous effluents. Journal of Water Process Engineering. 2022;47:102796. DOI: 10.1016/j.jwpe.2022.102796.

3. Hung K.-C., Chen B.-H., Yu L.E. Cloud-point extraction of selected polycyclic aromatic hydrocarbons by nonionic surfactants. Separation and Purification Technology. 2007;57(1):1-10. DOI: 10.1016/j.seppur.2007.03.004.

4. Silva W.P.N., do Nascimento A.E.G., de Alencar Moura M.C.P., de Oliveira H.N.M., de Barros Neto E.L. Study of phenol removal by cloud point extraction: a process optimization using experimental design. Separation and Purification Technology. 2015;152:133-139. DOI: 10.1016/j.seppur.2015.08.007.

5. Shilykovskaya D.O., Elokhov A.M., Denisova S.A., Lesnov A.E. Phase equilibria and extraction of metal ions in systems based on mixtures of oxyethylated nonylphenols. Izvestiya Akademii nauk. Seriya khimicheskaya. 2023;72(9):2036-2040. (In Russian). EDN: JSUGRW.

6. Isaeva Yu.I., Elokhov A.M., Denisova S.A., Kudryashova O.S. Phase equlibria and extraction of metal ions in systems based on mixtures of alkylbenzyldimethylammonium chloride and oxyethylated nonylphenols. Russian Journal of Physical Chemistry A. 2020;94(7):1346-1349. DOI: 10.1134/S0036024420070158.

7. Stankova A.V., Elokhov A.M., Lesnov A.E. Phase and extraction equilibria in the water – ethoxylated nonylphenol – sodium sulfate system. Izvestiya Akademii nauk. Seriya khimicheskaya. 2020;4:671-674. (In Russian). EDN: KJWYYM.

8. Elokhov A.M., Khomutova A.O., Denisova S.A. Phase equilibria and the extraction of metals in oxyethylated alkylamine – anionic surfactant – water systems. Russian Journal of Physical Chemistry A. 2021;95(6):1160-1164. DOI: 10.1134/s0036024421060108.

9. Laptedulche N.K., Gumerov F.M., Sergeeva E.S. Prospects of the use of ethoxylated high spirits for the purification of water. Energy saving and water treatment. 2011;6:16-18. (In Russian). EDN: ONRFCD.

10. Liu J.-L., Zhou X.-M., Sun M., Jia A.-Q., Shi H.-T., Zhang Q.-F. A resorcinarene based chelating agent for selective cloud point extraction of Pb2+ ions in water: synthesis, structural characterization and analytical applications. Arabian Journal of Chemistry. 2023;16(7):104866. DOI: 10.1016/j.arabjc.2023.104866.

11. Kori S. Cloud point extraction coupled with back extraction: a green methodology in analytical chemistry. Forensic Sciences Research. 2021;6(1):19-33. DOI: 10.1080/20961790.2019.1643567.

12. Kojro G., Wroczynski P. Cloud point extraction in the determination of drugs in biological matrices. Journal of Chromatographic Science. 2020;58(2):151-162. DOI: 10.1093/chromsci/bmz064.

13. Elokhov A.M., Kydryashova O.S., Lesnov A.E. Anionic surfactant in extraction. Bulletin of Perm University. Chemistry. 2015;1:30-43. (In Russian). EDN: SKSUJX.

14. Poteshnova M.V., Zadymova N.M. Features of the solubilizing effect of ethoxylated nonionic surfactants in relation to toluene in an aqueous environment. Vestnik moskovskogo universiteta. Seriya 2. Khimiya. 2002;43(3):185-189. (In Russian).

15. Mortada W.I. Recent developments and applications of cloud point extraction: a critical review. Microchemical Journal. 2020;157:105055. DOI: 10.1016/j.microc.2020.105055.

16. Elokhov A.M. Cloud point phenomenon in oxyethylated nonionic surfactants and water-soluble polymers solutions (review). I. Nature of phenomenon. Bulletin of Perm University. Chemistry. 2016;2:79-91. (In Russian). EDN: WJZQAR.

17. Shilykovskaya D.O., Denisova S.A., Elokhov A.M. Study of solubility and extraction ability of systems based on neonol mixtures AF 9-6 and AF 9-12. Vse materialy. entsiklopedicheskii spravochnik. 2022;14:30-35. (In Russian). DOI: 10.31044/1994-6260-2022-0-14-30-35. EDN: YDWNLS.

18. Shilykovskaya D.O., Elokhov A.M. Extractionspectrophotometric determination of nickel with 4-(2-pyridylazo) resorcinol in the neonol AF 9-10 – water system. Bulletin of Perm University. Chemistry. 2021;11(4):223-233. (In Russian). DOI: 10.17072/2223-1838-2021-4-223-233.

19. Stankova A.V., Elokhov A.M., Kudryashova O.S., Lesnov A.E. Temperature-induced transformation of phase diagrams for water – oxyethylated nonylphenol – MgCl2 systems. Russian Journal of Inorganic Chemistry. 2020;65(12):1922-1927. DOI: 10.1134/S0036023620120177.

20. Elokhov A.M. Phenomen of cloud point in oxyethylated nonionic surfactants and water-soluble polymers solutions (review). II. Inorganic salts influence on cloud point. Bulletin of Perm University. Chemistry. 2017;7(2):167-186. (In Russian). DOI: 10.17072/2223-1838-2017-2-167-186. EDN: ZFLVPH.

21. Arkhipov V.P., Arkhipov R.V., Idiyatullin Z.Sh. Extraction properties of aqueous solutions of ethoxylated isononylphenols in the presence of sodium salts with singly and doubly charged anions. Herald of Technological University. 2017;20(19):21-25. (In Russian). EDN: ZXFIQH.

22. Stankova A.V., Elokhov A.M., Denisova S.A., Kudryashova O.S., Lesnov A.E. Specific features of the salting-out of oxyethylated nonylphenols using inorganic salts at 25 °С. Russian Journal of Physical Chemistry A. 2017;91(5):880-886. DOI: 10.1134/S0036024417050247.

23. Idrisov A.R., Kuryashov D.A., Bashkirtsev N.Yu., Ismagilov I.F., Naisyrova A.M. Effect of low molecular weight salt on the structure of micellar surfactant solutions. Vestnik Kazanskogo tekhnologicheskogo universiteta. 2013;16(18):40-43. (In Russian). EDN: RCCRBZ.


Review

For citations:


Zholnerkevich V.I., Shrubok A.O. Gelation in the aqueous solutions of oxyethylated nonylphenols. Proceedings of Universities. Applied Chemistry and Biotechnology. 2025;15(1):112-118. (In Russ.) https://doi.org/10.21285/achb.965. EDN: UTPISA

Views: 46


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2227-2925 (Print)
ISSN 2500-1558 (Online)