Surface activity, micellization and solubilization of cationic gemini surfactant-conventional surfactants mixed systems

Journal of Molecular Liquids

Volumn 225, Issue , 2017, Pages 888-896

  Patel, U ^a   Parekh, P ^a   Sastry, N V ^b   Aswal, V K ^c   Bahadur, P ^a  

^a VEER NARMAD SOUTH GUJARAT UNIVERSITY   (India)

^b SARDAR PATEL UNIVERSITY   (India)

^c BHABHA ATOMIC RESEARCH CENTRE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBONS; MICELLES; NAPHTHALENE; NEUTRON SCATTERING; POLYCYCLIC AROMATIC HYDROCARBONS; SOLUBILITY; SURFACE ACTIVE AGENTS;

CATIONIC GEMINI SURFACTANT; CRITICAL MICELLES CONCENTRATIONS; DODECYL TRIMETHYL AMMONIUM BROMIDE; MOLAR SOLUBILIZATION RATIOS; POLYCYCLIC AROMATIC HYDROCARBONS (PAHS); SOLUBILIZATION CAPACITIES; SURFACE EXCESS CONCENTRATION; WATER PARTITION COEFFICIENTS;

CATIONIC SURFACTANTS;

EID: 85006741789     PISSN: 01677322     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molliq.2016.11.017     Document Type: Article

References (72)

1. [1] Ogino, K., Abe, M., Mixed Surfactant Systems. 1992, CRC Press.
2. [2] Bakshi, M.S., et al. Mixed micelles of cationic 12-2-12 gemini with conventional surfactants: the head group and counterion effects. Colloids Surf. A Physicochem. Eng. Asp. 237 (2004), 61–71.
3. [3] Szymczyk, K., et al. The properties of mixtures of two cationic surfactants in water at water/air interface. Colloids Surf. A Physicochem. Eng. Asp. 264 (2005), 147–156.
4. [4] Al-Wardian, A., Glenn, K.M., Palepu, R.M., Thermodynamic and interfacial properties of binary cationic mixed systems. Colloids Surf. A Physicochem. Eng. Asp. 247 (2004), 115–123.
5. [5] Chakraborty, T., Ghosh, S., Moulik, S.P., Micellization and related behavior of binary and ternary surfactant mixtures in aqueous medium: cetyl pyridinium chloride (CPC), cetyl trimethyl ammonium bromide (CTAB), and polyoxyethylene (10) cetyl ether (Brij-56) derived system. J. Phys. Chem. 109 (2005), 14813–14823.
6. [6] Das, S., Maiti, S., Ghosh, S., Synthesis of two biofriendly anionic surfactants (N-n-decanoyl-L-valine and N-n-decanoyl-L leucine) and its mixed micellization with nonionic surfactant Mega-10 in tris-buffer medium at pH 9. RSC Adv. 4 (2014), 12275–12286.
7. [7] Ghosh, S., Surface chemical and micellar properties of binary and ternary surfactant mixtures (cetyl pyridinium chloride, Tween-40, and Brij-56) in an aqueous medium. J. Colloid Interface Sci. 244 (2001), 128–138.
8. [8] Tsubone, K., The interaction of an anionic gemini surfactant with conventional anionic surfactants. J. Colloid Interface Sci. 261 (2003), 524–528.
9. [9] Islam, M.N., Kato, T., Adsorption and micellar properties of a mixed system of nonionic–nonionic surfactants. J. Colloid Interface Sci. 289 (2005), 581–587.
10. [10] Ghosh, S., et al. Interfacial and self-aggregation of binary mixtures of anionic and nonionic amphiphiles in aqueous medium. J. Phys. Chem. 115 (2011), 11098–11112.
11. [11] Haque, M.E., et al. Properties of mixed micelles of binary surfactant combinations. Langmuir 12 (1996), 4084–4089.
12. [12] Yin, H., et al. Two-phase region in the DTAB/SL mixed surfactant system. Langmuir 18 (2002), 9198–9203.
13. [13] Miraglia, D.B., et al. Effect of the concentration and composition on the size and shape of micelles of sodium oleate–cetyltrimethylammonium bromide mixtures. J. Colloid Interface Sci. 351 (2010), 197–202.
14. [14] Høiland, H., et al. Solubilization of alcohols in SDS and TTAB from isentropic partial molar compressibilities and solubilities. Colloids Surf. A Physicochem. Eng. Asp. 183 (2001), 651–660.
15. [15] Ghosh, S., Ray, G.B., Mondal, S., Physicochemical investigation on the bulk and surface properties of the binary mixtures of N-methyl-N-dodecanoyl sodium glycinate (SDDS) and N-methyl-N-decanoyl glucamine (MEGA 10) in aqueous medium. Fluid Phase Equilib. 405 (2015), 46–54.
16. [16] Matsuoka, K., Lee, J., Moroi, Y., Micellization of bile salts and solubilization into the micelles. J. Surf. Sci. Technol. 26 (2010), 105–136.
17. [17] Parekh, P., et al. Anionic–cationic mixed surfactant systems: micellar interaction of sodium dodecyl trioxyethylene sulfate with cationic gemini surfactants. Colloids Surf. A Physicochem. Eng. Asp. 385 (2011), 111–120.
18. [18] Zana, R., Xia, J., Gemini Surfactants: Synthesis, Interfacial and Solution-Phase Behavior, and Applications. 2003, CRC Press.
19. [19] Zhu, S., et al. Anionic gemini surfactants: synthesis and aggregation properties in aqueous solutions. Colloids Surf. A Physicochem. Eng. Asp. 281 (2006), 35–39.
20. [20] Yoshimura, T., Esumi, K., Synthesis and surface properties of anionic gemini surfactants with amide groups. J. Colloid Interface Sci. 276 (2004), 231–238.
21. [21] Tsubone, K., Ghosh, S., Micelle ionization degree of anionic gemini surfactant having N, N-dialkylamide and carboxylate groups. J. Surfactant Deterg. 6 (2003), 225–229.
22. [22] Chakraborty, T., Ghosh, S., Mixed micellization of an anionic gemini surfactant (GA) with conventional polyethoxylated nonionic surfactants in brine solution at pH 5 and 298 K. Colloid Polymer Sci. 285 (2007), 1665–1673.
23. [23] Sharma, V., et al. Synthesis, characterization, and SANS studies of novel alkanediyl-α, ω-bis (hydroxyethylmethylhexadecylammonium bromide) cationic gemini surfactants. J. Colloid Interface Sci. 277 (2004), 450–455.
24. [24] Das, S., Naskar, B., Ghosh, S., Influence of temperature and organic solvents (isopropanol and 1, 4-dioxane) on the micellization of cationic gemini surfactant (14-4-14). Soft Matter 10 (2014), 2863–2875.
25. [25] Das, S., et al. Physicochemical behaviors of cationic gemini surfactant (14-4-14) based microheterogeneous assemblies. Langmuir 30 (2014), 12483–12493.
26. [26] Tikariha, D., et al. Interaction between cationic gemini and monomeric surfactants: micellar and surface properties. J. Nano fluids 2 (2013), 316–324.
27. [27] Sharma, P., Sachar, S., Kaur, G., Thakur, P., Bakshi, S.M., Banipal, T.S., Mixed micelle behaviour of Dodecyl-β-D-glucopyranoside with cationic gemini surfactants: a fluorescence study. J. Surf. Sci. Technol. 23:3–4 (2007), 131–147.
28. [28] FitzGerald, P.A., et al. Preparation and dilute solution properties of model gemini nonionic surfactants. J. Colloid Interface Sci. 275 (2004), 649–658.
29. [29] Sikirić, M., et al. Effect of the spacer length on the association and adsorption behavior of dissymmetric gemini surfactants. J. Colloid Interface Sci. 281 (2005), 473–481.
30. [30] Borse, M., et al. Effect of head group polarity and spacer chain length on the aggregation properties of gemini surfactants in an aquatic environment. J. Colloid Interface Sci. 284 (2005), 282–288.
31. [31] Singh, K., Marangoni, D.G., Synergistic interactions in the mixed micelles of cationic gemini with zwitterionic surfactants: the pH and spacer effect. J. Colloid Interface Sci. 315 (2007), 620–626.
32. [32] Siddiqui, U.S., Kumar, S., Viscometric studies on aqueous gemini micelles in the presence of additives. Colloids Surf. A Physicochem. Eng. Asp. 301 (2007), 209–213.
33. [33] Oliviero, C., et al. Gemini surfactant–water mixtures: some physical–chemical properties. Colloids Surf. A Physicochem. Eng. Asp. 201 (2002), 247–260.
34. [34] Ali, M.S., et al. Interactions between cationic gemini/conventional surfactants with polyvinylpyrrolidone: specific conductivity and dynamic light scattering studies. Colloids Surf. A Physicochem. Eng. Asp. 350 (2009), 51–56.
35. [35] Murguía, M.C., et al. Synthesis, surface-active properties, and antimicrobial activities of new neutral and cationic trimeric surfactants. J. Surfactant Deterg. 11 (2008), 41–48.
36. [36] Chavda, S., Bahadur, P., Micellization of a cationic gemini surfactant in aqueous solutions with different alkanols and alkanediols as additives: effect of nonpolar chain and position of hydroxyl groups. J. Mol. Liq. 161 (2011), 72–77.
37. [37] Li, F., Rosen, M.J., Sulthana, S.B., Surface properties of cationic gemini surfactants and their interaction with alkylglucoside or-maltoside surfactants. Langmuir 17 (2001), 1037–1042.
38. [38] Bakshi, M.S., et al. Mixed micelle behavior of Pluronic L64 and Triton X-100 with conventional and dimeric cationic surfactants. J. Colloid Interface Sci. 286 (2005), 369–377.
39. [39] Esumi, K., et al. Mixed micellar properties of a cationic gemini surfactant and a nonionic surfactant. Colloids Surf. A Physicochem. Eng. Asp. 135 (1998), 117–122.
40. [40] 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 56 (2011), 2647–2654.
41. [41] De, S., et al. Role of spacer chain length in dimeric micellar organization. Small angle neutron scattering and fluorescence studies. J. Phys. Chem. 100 (1996), 11664–11671.
42. [42] 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. 111 (2007), 3122–3132.
43. [43] Edwards, D.A., Luthy, R.G., Liu, Z., Solubilization of polycyclic aromatic hydrocarbons in micellar nonionic surfactant solutions. Environ. Sci. Technol. 25 (1991), 127–133.
44. [44] Fatma, N., Panda, M., Ansari, W.H., Solubility enhancement of anthracene and pyrene in the mixtures of a cleavable cationic gemini surfactant with conventional surfactants of different polarities. Colloids Surf. A Physicochem. Eng. Asp. 467 (2015), 9–17.
45. [45] Lakra, J., et al. Mixed micellization of gemini and cationic surfactants: physicochemical properties and solubilization of polycyclic aromatic hydrocarbons. Colloids Surf. A Physicochem. Eng. Asp. 451 (2014), 56–65.
46. [46] 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. 167 (2009), 575–581.
47. [47] Chun, C.L., Lee, J.-J., Park, J.-W., Solubilization of PAH mixtures by three different anionic surfactants. Environ. Pollut. 118 (2002), 307–313.
48. [48] Bernardez, L.A., Ghoshal, S., Solubilization kinetics for polycyclic aromatic hydrocarbons transferring from a non-aqueous phase liquid to non-ionic surfactant solutions. J. Colloid Interface Sci. 320 (2008), 298–306.
49. [49] Bernardez, L.A., Effects of flow rate and temperature on the dissolution of polycyclic aromatic hydrocarbons transferring from a nonaqueous phase liquid to nonionic surfactant solutions. Chem. Eng. Commun. 199 (2012), 151–163.
50. [50] Jiang, Y., et al. NMR study of the dynamics of cationic Gemini surfactant 14 − 2 − 14 in mixed solutions with conventional surfactants. J. Phys. Chem. 113 (2009), 8357–8361.
51. [51] Hait, S., Moulik, S., Gemini surfactants: a distinct class of self-assembling molecules. Curr. Sci. Bangalore 82 (2002), 1101–1111.
52. [52] Bucci, S., et al. Small-angle neutron-scattering study of ionic-nonionic mixed micelles. Langmuir 7 (1991), 824–826.
53. [53] De, S., et al. Small-angle neutron scattering studies of different mixed micelles composed of dimeric and monomeric cationic surfactants. J. Phys. Chem. 101 (1997), 5639–5645.
54. [54] Goyal, P., Aswal, V., Micellar structure and inter-micelle interactions in micellar solutions: results of small angle neutron scattering studies. Curr. Sci. Bangalore 80 (2001), 972–979.
55. [55] Moroi, Y., et al. Solubilization of benzene, naphthalene, anthracene, and pyrene in 1-dodecanesulfonic acid micelle. J. Phys. Chem. 99 (1995), 2372–2376.
56. [56] Patel, V., et al. Triton X-100 micelles modulated by solubilized cinnamic acid analogues: the pH dependant micellar growth. Colloids Surf. A Physicochem. Eng. Asp. 450 (2014), 106–114.
57. [57] Kumar, S., Aswal, V.K., Kohlbrecher, J., Size-dependent interaction of silica nanoparticles with different surfactants in aqueous solution. Langmuir 28 (2012), 9288–9297.
58. [58] Rosen, M.J., Sulthana, S.B., The interaction of alkylglycosides with other surfactants. J. Colloid Interface Sci. 239 (2001), 528–534.
59. [59] Sheikh, M.S., Dar, A.A., Interaction of a cationic gemini surfactant with conventional surfactants in the mixed micelle and monolayer formation in aqueous medium. J. Colloid Interface Sci. 333 (2009), 605–612.
60. [60] Zana, R., Bolaform and dimeric (gemini) surfactants, in specialist surfactants. Springer, 1997, 81–103.
61. [61] Zana, R., Benrraou, M., Rueff, R., Alkanediyl-alpha, omega.-bis (dimethylalkylammonium bromide) surfactants. 1. Effect of the spacer chain length on the critical micelle concentration and micelle ionization degree. Langmuir 7 (1991), 1072–1075.
62. [62] Clint, J.H., Micellization of mixed nonionic surface active agents. J. Chem. Soc. Faraday Trans. 1 Phys. Chem. Condens. Phases 71 (1975), 1327–1334.
63. [63] Tanford, C., The Hydrophobic Effect: Formation of Micelles and Biological Membranes. second ed., 1980, J. Wiley.
64. [64] Maeda, H., Dodecyldimethylamine oxide micelles: stability, aggregation number and titration properties. Colloids Surf. A Physicochem. Eng. Asp. 109 (1996), 263–271.
65. [65] Ruiz, C.C., Aguiar, J., Interaction, stability, and microenvironmental properties of mixed micelles of Triton X100 and n-alkyltrimethylammonium bromides: influence of alkyl chain length. Langmuir 16 (2000), 7946–7953.
66. [66] 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. 114 (2010), 6023–6032.
67. [67] Bai, G., et al. Thermodynamics of molecular self-assembly of cationic gemini and related double chain surfactants in aqueous solution. J. Phys. Chem. 105 (2001), 3105–3108.
68. [68] Sharma, K.S., et al. Studies of mixed surfactant solutions of cationic dimeric (gemini) surfactant with nonionic surfactant C 12 E 6 in aqueous medium. J. Colloid Interface Sci. 268 (2003), 482–488.
69. [69] Israelachvili, J.N., Mitchell, D.J., Ninham, B.W., Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers. J. Chem. Soc. Faraday Trans. 2 Mol. Chem. Phys. 72 (1976), 1525–1568.
70. [70] Dar, A.A., et al. Mixed micellization and interfacial properties of dodecyltrimethylammonium bromide and tetraethyleneglycol mono-n-dodecyl ether in absence and presence of sodium propionate. J. Colloid Interface Sci. 298 (2006), 395–405.
71. [71] Flory, P.D., Statistical thermodynamics of liquid mixtures. J. Am. Chem. Soci. 87 (1965), 1833–1838.
72. [72] Dharaiya, N., Aswal, V.K., Bahadur, P., Characterization of Triton X-100 and its oligomer (Tyloxapol) micelles vis-à-vis solubilization of bisphenol A by spectral and scattering techniques. Colloids Surf. A Physicochem. Eng. Asp. 470 (2015), 230–239.