Enhanced aqueous solubility of naphthalene and pyrene by binary and ternary Gemini cationic and conventional nonionic surfactants

Chemosphere

Volumn 89, Issue 11, 2012, Pages 1347-1353

  Wei, Jia ^a   Huang, Guohe ^a   Zhu, Lei ^b   Zhao, Shan ^a   An, Chunjiang ^a   Fan, Yurui ^a  

^a UNIVERSITY OF REGINA   (Canada)

^b BEIJING INSTITUTE OF GRAPHIC COMMUNICATION   (China)

Author keywords

Gemini; Multi component surfactant systems; Polycyclic aromatic hydrocarbon; Solubilization

Indexed keywords

CATIONIC SURFACTANTS; DYES; FREE ENERGY; MICELLES; MINERAL OILS; MOLAR RATIO; NAPHTHALENE; POLYCYCLIC AROMATIC HYDROCARBONS; PYRENE; SOLUBILITY;

GEMINI; GEMINI CATIONIC SURFACTANTS; MOLAR SOLUBILIZATION RATIOS; POLYCYCLIC AROMATIC HYDROCARBONS (PAHS); SOLUBILIZATION; SURFACTANT SYSTEM; TERNARY SURFACTANT SYSTEMS; WATER PARTITION COEFFICIENTS;

NONIONIC SURFACTANTS;

CATIONIC SURFACTANT; GEMINI; IONIC SURFACTANT; NAPHTHALENE; POLYCYCLIC AROMATIC HYDROCARBON; PYRENE; UNCLASSIFIED DRUG; WATER;

CATION; CHEMICAL PROPERTY; COLLOID; NAPHTHALENE; ORGANIC COMPOUND; PAH; PYRENE; SOLUBILITY; SOLUBILIZATION; SOLUTE; SURFACTANT; SYNERGISM; TENSIOMETER;

AQUEOUS SOLUTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL PARAMETERS; CHEMICAL REACTION; CONTROLLED STUDY; ENERGY; MEASUREMENT; MICELLE; MOLAR SOLUBILIZATION RATIO; SOLUBILITY; SURFACE TENSION MEASUREMENT;

EID: 84866608965     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2012.05.091     Document Type: Article

References (44)

1. Atkins A., Bignal K.L., Zhou J.L., Cazier F. Profiles of polycyclic aromatic hydrocarbons and polychlorinated biphenyls from the combustion of biomass pellets. Chemosphere 2010, 78:1385-1392.
2. Berthod A., Tomer S., Dorsey J.G. Polyoxyethylene alkyl ether nonionic surfactants: physicochemical properties and use for cholesterol determination in food. Talanta 2001, 55:69-83.
3. Burman A.D., Dey T., Mukherjee B., Das A.R. Solution properties of the binary and ternary combination of sodium dodecyl benzene sulfonate, polyoxyethylene sorbitan monlaurate, and polyoxyethylene lauryl ether. Langmuir 2000, 16:10020-10027.
4. Rangel-Yagui C.O., Hsu H.W.L., Pessoa A., Tavares L.C. Micellar solubilization of ibuprofen: influence of surfactant head groups on the extent of solubilization. Braz. J. Pharm. Sci. 2005, 41:237-246.
5. Chavda S., Kuperkar K., Bahadur P. Formation and growth of gemini surfactant (12-s-12) micelles as a modulate by spacers: a thermodynamic and small-angle neutron scattering (SANS) study. J. Chem. Eng. Data 2011, 56:2647-2654.
6. Clint J.H. Micellization of mixed nonionic surface active agents. J. Chem. Soc. Faraday Trans. 1974, 71:1327-1334.
7. Dar A.A., Rather G.M., Das A.R. Mixed micelle formation and solubilization behavior toward polycyclic aromatic hydrocarbons of binary and ternary cationic-nonionic surfactant mixtures. J. Phys. Chem. B 2007, 111:3122-3132.
8. Din K.U., Sheikh M.S., Dar A.A. Analysis of mixed micellar and interfacial behavior of cationic gemini hexanediyl-1,6-bis(dimethylcetylammonium bromide) with conventional ionic and nonionic surfactants in aqueous medium. J. Phys. Chem. B 2010, 114:6023-6032.
9. Edwards D.A., Luthy R.G., Liu Z. Solubilization of polycyclic aromatic hydrocarbons in micellar nonionic surfactant solutions. Environ. Sci. Technol. 1991, 25:127-133.
10. Gan S., Lau E.V., Ng H.K. Remediation of soils contaminated with polycyclic aromatic hydrocarbons (PAHs). J. Hazard. Mater. 2009, 172:532-549.
11. Guo C., Zhou P., Shao J., Yang X., Shang Z. Integrating statistical and experimental protocols to model and design novel Gemini surfactants with promising critical micelle concentration and low environmental risk. Chemosphere 2011, 84:1608-1616.
12. Holland P.M., Rubingh D.N. Nonideal multicomponent mixed micelle model. J. Phys. Chem. 1983, 87:1984-1990.
13. 42 with a cationic gemini surfactant in aqueous solutions. J. Colloid Interface Sci. 2011, 356:605-613.
14. Kabir ud D., Shafi M., Bhat P.A., Dar A.A. Solubilization capabilities of mixtures of cationic Gemini surfactant with conventional cationic, nonionic and anionic surfactants towards polycyclic aromatic hydrocarbons. J. Hazard. Mater. 2009, 167:575-581.
15. Khan I.A., Khanam A.J., Sheikh M.S., Kabir ud D. Influence of ionic and nonionic hydrotropes on micellar behavior of a cationic gemini surfactant butanediyl-1,4-bis(dimethylcetylammonium bromide). J. Colloid Interface Sci. 2011, 359:467-473.
16. Kile D.E., Chiou C.T. Water solubility enhancements of DDT and trichlorobenzene by some surfactants below and above the critical micelle concentration. Environ. Sci. Technol. 1989, 23:832-838.
17. Li J.L., Chen B.H. Solubilization of model polycyclic aromatic hydrocarbons by nonionic surfactants. Chem. Eng. Sci. 2002, 57:2825-2835.
18. Rosen M.J. Micelle Formation by Surfactants 1989, John Wiley and Sons, New York.
19. Madni I., Hwang C.Y., Park S.D., Choa Y.H., Kim H.T. Mixed surfactant system for stable suspension of multiwalled carbon nanotubes. Colloids Surf. A 2010, 358:101-107.
20. Mehta S.K., Chaudhary S., Kumar R., Bhasin K.K. Facile solubilization of organochalcogen compounds in mixed micelle formation of binary and ternary cationic-nonionic surfactant mixtures. J. Phys. Chem. B 2009, 113:7188-7193.
21. Menger F.M., Littau C.A. Gemini surfactants: a new class of self-assembling molecules. J. Am. Chem. Soc. 1993, 115:10083-10090.
22. Mir M.A., Chat O.A., Najar M.H., Younis M., Dar A.A., Rather G.M. Solubilization of triphenylamine, triphenylphosphine, triphenylphosphineoxide and triphenylmethanol in single and binary surfactant systems. J. Colloid Interface Sci. 2011, 364:163-169.
23. Moulik S.P., Haque M.E., Jana P.K., Das A.R. Micellar properties of cationic surfactants in pure and mixed states. J. Phys. Chem. 1996, 100:701-708.
24. Mulligan C.N., Yong R.N., Gibbs B.F. Surfactant-enhanced remediation of contaminated soil: a review. Eng. Geol. 2001, 60:371-380.
25. Petitgirard A., Djehiche M., Persello J., Fievet P., Fatin-Rouge N. PAH contaminated soil remediation by reusing an aqueous solution of cyclodextrins. Chemosphere 2009, 75:714-718.
26. Rao K.J., Paria S. Solubilization of naphthalene in the presence of plant-synthetic mixed surfactant systems. J. Phys. Chem. B 2008, 113:474-481.
27. Rubingh D.N. Solution Chemistry of Surfactants 1979, Plenum, New York.
28. Sales P.S., de Rossi R.H., Fernández M.A. Different behaviours in the solubilization of polycyclic aromatic hydrocarbons in water induced by mixed surfactant solutions. Chemosphere 2011, 84:1700-1707.
29. Sharma K.S., Hassan P.A., Rakshit A.K. Self aggregation of binary surfactant mixtures of a cationic dimeric (gemini) surfactant with nonionic surfactants in aqueous medium. Colloids Surf. A 2006, 289:17-24.
30. 6 in aqueous medium. J. Colloid Interface Sci. 2003, 268:482-488.
31. Sheikh M.S., Kabir ud D., Dar A.A. Synergistic interaction of Gemini surfactant pentanediyl-1,5-bis(dimethylcetylammonium bromide) with conventional (ionic and nonionic) surfactants and its impact on the solubilization. Colloids Surf. A 2011, 378:60-66.
32. Sun Y., Feng Y., Dong H., Chen Z. Adsorption of dissymmetric cationic gemini surfactants at silica/water interface. Surface Sci. 2007, 601:1988-1995.
33. Tan H., Xiao H. Synthesis and antimicrobial characterization of novel l-lysine gemini surfactants pended with reactive groups. Tetrahedron Lett. 2008, 49:1759-1761.
34. Tanford C. The Hydrophobic Effect: Formation of Micelles and Biological Membranes 1980, John Wiley and Sons, New York.
35. Verschueren K. Handbook of Environmental Data on Organic Chemicals 1996, John Wiley and Sons, New York. third ed.
36. Vilasau J., Solans C., Gómez M.J., Dabrio J., Mújika-Garai R., Esquena J. Phase behaviour of a mixed ionic/nonionic surfactant system used to prepare stable oil-in-water paraffin emulsions. Colloids Surf. A 2011, 384:473-481.
37. Wang X., Wang J., Wang Y., Ye J., Yan H., Thomas R.K. Properties of mixed micelles of cationic gemini surfactants and nonionic surfactant triton X-100: effects of the surfactant composition and the spacer length. J. Colloid Interface Sci. 2005, 286:739-746.
38. Wei J., Huang G., Yu H., An C. Efficiency of single and mixed Gemini/conventional micelles on solubilization of phenanthrene. Chem. Eng. J. 2011, 168:201-207.
39. Wu Y., Teng Y., Li Z., Liao X., Luo Y. Potential role of polycyclic aromatic hydrocarbons (PAHs) oxidation by fungal laccase in the remediation of an aged contaminated soil. Soil Biol. Biochem. 2008, 40:789-796.
40. Moroi Y. Micelles: Theoretical and Applied Aspects 1992, Plenum, New York.
41. Zana R. Dimeric and Oligomeric Surfactants. Behavior at Interfaces and in Aqueous Solution: A Review. Adv. Colloid Interface Sci. 2002, 97:205-253.
42. Zhou W., Zhu L. Solubilization of pyrene by anionic-nonionic mixed surfactants. J. Hazard. Mater. 2004, 109:213-220.
43. Zhou W., Zhu L. Solubilization of polycyclic aromatic hydrocarbons by anionic-nonionic mixed surfactant. Colloids Surf. A 2005, 255:145-152.
44. Zhou W., Zhu L. Enhanced soil flushing of phenanthrene by anionic-nonionic mixed surfactant. Water Res. 2008, 42:101-108.