Startseite Synthesis and Properties of a Series of CO2 Switchable Gemini Imidazolium Surfactants
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Synthesis and Properties of a Series of CO2 Switchable Gemini Imidazolium Surfactants

  • Hongsheng Lu , Yu He und Zhiyu Huang
Veröffentlicht/Copyright: 25. September 2014
Veröffentlichen auch Sie bei De Gruyter Brill

Abstract

Novel switchable gemini imidazolium surfactants with different carbon atoms in hydrophobic group were successfully synthesized by condensation of fatty acid with triethylene tetramine, then the intermediates were reacted with CO2 to give the imidazolinium bicarbonates. The structures of intermediates and products were identified by IR and 1H-NMR spectra. As the results show, the structures of the products obtained correspond to the target compounds designed. By surface tension measurements, these Gemini surfactants have excellent surface activity with low cmc and surface tension. The conductivity and surface tension cycles show that these surfactants could be switched from imidazoline (neutral form) to imidazolium bicarbonate (charged form) reversibly and repeatedly.

Kurzfassung

Es wurden neue schaltbare Gemini-Imidazolintenside mit unterschiedlicher Anzahl an Kohlenstoffatomen in der hydrophoben Gruppe durch Kondensation von Fettsäuren mit Triethylentetramin und anschließender Reaktion der Zwischenprodukte mit CO2 zu den Imidazoliumbicarbonaten synthetisiert. Die Struktur der Zwischen- und Endprodukte wurden mittels IR- und 1H-NMR-Spektren festgestellt. Die Ergebnisse zeigen, dass die Strukturen der erhaltenen Produkte denen der erwünschten Zielprodukte entsprechen. Messungen der Oberflächenspannung zeigen, dass die Gemini-Tenside eine hervorragende Oberflächenaktivität mit einer geringen cmc und Oberflächenspannung bei der cmc aufweisen. Die Leitfähigkeit und die Oberflächenspannungszyklen zeigen, dass die Tenside zwischen ihrer Imidazolin-Form (ohne Ladung) und ihrer Imidazoliumbicarbonat-Form (geladene Form) hin und her geschaltet werden können.


* Correspondence address Dr. Hongsheng Lu, School of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, P. R. China. Tel.: +8628 83037305, Fax: +8628 83037305, E-Mail:

Dr Hongsheng Lu is currently associate professor at the College of Chemistry and Chemical Engineering, Southwest Petroleum University. He received his Ph.D. in Chengdu Institute of Organic Chemistry of Chinese Academy of Science. His research interests include synthesis and application of oil chamicals.

Mr. Yu He is currently a M.D. candidate at the College of Chemistry and Chemical Engineering, Southwest Petroleum University. His main research is synthesis and application of novel CO2 switchable surfactants.

Prof. Zhiyu Huang is currently the director of Gradate School, Southwest Petroleum University. He received his Ph.D. in Applied Chemistry at the college of Chemistry and Chemical Engineering, Southwest Petroleum University. His research interests include synthesis and application of oil chamicals.


References

1. Liu, Y., Jessop, P. G., Cunningham, M., Eckert, C. A. and Liotta, C. L.: Switchable surfactants, Science313 (2006) 958. DOI: 10.1126/science.1128142Suche in Google Scholar PubMed

2. Arthur, T., Harjani, J., Jessop, P. G. and Hodson, P. V.: Effects-driven chemical design: the acute toxicity of CO2-triggered switchable surfactants to rainbow trout can be predicted from octanol-water partition coefficients, Green Chemistry14 (2012) 357. DOI: 10.1039/C1GC15620ASuche in Google Scholar

3. Mihar, M., Jessop, P. G. and Cunningha, F.: Redispersible polymer colloids using carbon dioxide as an external stimulus, Macromolecules44 (2011) 3688. DOI: 10.1021/ma200249qSuche in Google Scholar

4. Jessop, P. G., Mercer, S. M. and Heldebrant, D. J.: CO2-triggered switchable solvents, surfactants, and other materials, Energy & Environmental Science5 (2012) 7240. DOI: 10.1039/C2EE02912JSuche in Google Scholar

5. Pinaud, J., Kowal, E., Cunningham, M. and Jessop, P. G.: 2-(Diethyl)aminoethyl methacrylate as a CO2-switchable co-monomer for the preparation of readily coagulated and redispersed polymer latexes, ACS Macro Letters1 (2012) 1103. DOI: 10.1021/mz3003215Suche in Google Scholar PubMed

6. Fowler, C. A., Jessop, P. G. and Cunningham, M.: Emulsion polymerization of styrene and methyl methacrylate using cationic switchable surfactants, Macromolecules44 (2011) 2501. DOI: 10.1021/ma102936aSuche in Google Scholar

7. Chen, L., Harjani, J. R., Robert, T., Rogel, E., Kuehne, D., Ovalles, C., Sampath, V. and Jessop, P. G.: Use of CO2-triggered switchable surfactants for the stabilization of heavy crude oil-in-water emulsions, Energy Fuels26 (2012) 488. DOI: 10.1021/ef200701 gSuche in Google Scholar

8. Holland, A., Wechsler, D., Patel, A., Molloy, B. M., Boyd, A. R. and Jessop, P. G.: Separation of bitumen from oil sands using a switchable hydrophilicity solvent, Can. J. Chem.90 (2012) 1. DOI: 10.1139/v2012-061Suche in Google Scholar

9. Zhang, Y., Feng, Y., Wang, J., He, S., Guo, Z., Chu, Z. and Dreiss, C. A.: CO2-switchable wormlike micellesChemical communications49 (2013) 4902. DOI: 10.1039/C3CC41059ESuche in Google Scholar

10. Zhang, Y., Feng, Y., Wang, Y. and Li, X.: CO2-switchable viscoelastic fluids based on a pseudogemini surfactant, Langmuir29 (2013) 4187. DOI: 10.1021/la400051aSuche in Google Scholar PubMed

11. Lu, H., He, Y. and Huang, Zh.: Foaming properties of CO2-triggered surfactants for switchable foam control, Journal of Dispersion Science and Technology. DOI: 10.1080/01932691.2013.817951.Suche in Google Scholar

12. Zana, R., Adv.: Dimeric and oligomeric surfactants. Behavior at interfaces and in aqueous solution: a review, J. Colloid. Interface. Sci.97 (2002) 20. DOI: 10.1016/s0001-8686(01)00069-0Suche in Google Scholar PubMed

13. Zana, R. and Xia, J.: Gemini Surfactants: Synthesis, Interfacial and Solution-Phase Behavior, and Applications, Marcel Dekker, New York (2004). DOI: 10.1016/j.jcis.2003.12.054Suche in Google Scholar

14. Zana, R.: Dimeric (Gemini) Surfactants: Effect of the spacer group on the association behavior in aqueous solution, J Colloid Interface Sci.248 (2002) 203. DOI: 10.1006/jcis.2001.8104Suche in Google Scholar PubMed

15. Zana, R. and Talmon, Y.: Dependence of aggregate morphology on structure of dimeric surfactants, Nature362 (1993) 228. DOI: 10.1038/362228a0Suche in Google Scholar

16. Han, L., Ye, Zh., Chen, H. and Luo, P.: The interfacial tension between cationic gemini surfactant solution and crude oil, Surf. Sci.552 (2004) L53. DOI: 10.1007/s11743-009-1109-7Suche in Google Scholar

17. Huo, Q., Leon, R., Petroff, P. M., and Stucky, G. D.: Mesostructure design with gemini surfactants: supercage formation in a three-dimensional hexagonal array, Science268 (1995) 1324. DOI: 10.1126/science.268.5215.1324Suche in Google Scholar PubMed

18. Badea, I., Wettig, S., Verrall, R. and Foldvari, M.: Topical non-invasive gene delivery using gemini nanoparticles in interferon-gamma-deficient mice, Eur. J. Pharmacol. Biopharmacol.65 (2007) 414. DOI: 10.1016/j.ejpb.2007.01.002Suche in Google Scholar PubMed

19. Wettig, S. D., Nowak, P. and Verrall, R. E.: Thermodynamic and aggregation properties of gemini surfactants with hydroxyl substituted spacers in aqueous solution, Langmuir18 (2002) 5354. DOI: 10.1021/la011782sSuche in Google Scholar

20. Aiad, I., Emam, D., El-Deeb, A. and Abd-Alrahman, E.: Novel imidazolium-based gemini surfactants: synthesis, surface properties, corrosion inhibition and biocidal activity against sulfate-reducingbacteria, J. Surfact. Deterg.1 (2013). DOI: 10.1007/s11743-013-1491-z.Suche in Google Scholar

21. Patial, P., Shaheen, A. and Ahmad, I.: Synthesis, characterization and evaluation of the surface active properties of novel cationic imidazolium gemini surfactants, J. Surfact. Deterg.1 (2013). DOI: 10.1007/s11743-013-1472-2.Suche in Google Scholar

22. Wang, S., Furuno, T. and Cheng, Z.: Synthesis of 1-hydroxyethyl-2-alkyl-2-imidazoline and its derivative sulfonate amphoteric surfactant from tall oil fatty acid, J. Wood Sci.49 (2003) 371, DOI: 10.1007/s10086-002-0476-8.Suche in Google Scholar

23. Scott, L. M., Robert, T., Harjani, J. R. and Jessop, P. G.: Designing the head group of CO2-triggered switchable surfactants, RSC Advances2 (2012) 4925. DOI: 10.1039/C2RA01242ASuche in Google Scholar

24. HinesJ. D., GarrettP. R., RennieG. K., ThomasR. K. and PenfoldJ. J.: Structure of an absorbed layer of n-dodecyl-N,N-dimethylamino acetate at the air/solution interface as determined by neutron reflection, Phys. Chem. B101 (1997) 7121. DOI: 10.1021/jp9711959Suche in Google Scholar

25. Eastoe, J., Nave, S., Downer, A., Paul, A., Rankin, A., Tribe, K. and Penfold, J.: Adsorption of ionic surfactants at the air-solution interface, Langmuir16 (2000) 4511. DOI: 10.1021/la991564nSuche in Google Scholar

26. Fowler, C. I., Jessop, P. G. and Cunningham, M.: Aryl amidine and tertiary amine switchable surfactants and their application in the emulsion polymerization of methyl methacrylate, Macromolecules45 (2012) 2955. DOI: 10.1021/ma2027484Suche in Google Scholar

27. Zana, R.: Critical micellization concentration of surfactants in aqueous solution and free energy of micellization, Langmuir12 (1996) 1208. DOI: 10.1021/la950691qSuche in Google Scholar

Received: 2013-10-10
Revised: 2014-04-08
Published Online: 2014-09-25
Published in Print: 2014-09-15

© 2014, Carl Hanser Publisher, Munich

Heruntergeladen am 9.10.2025 von https://www.degruyterbrill.com/document/doi/10.3139/113.110323/html
Button zum nach oben scrollen