Micellar properties of zwitterionic surfactant - alkoxyethanol mixed micelles

2004 ◽  
Vol 82 (7) ◽  
pp. 1223-1229 ◽  
Author(s):  
Maria K Mullally ◽  
D Gerrard Marangoni
Keyword(s):  
Mixed Micelles ◽  
Hydrophobic Interactions ◽  
Mixed Solvents ◽  
Sodium Dodecylsulfate ◽  
Micelle Formation ◽  
Alcohol Concentration ◽  
Zwitterionic Surfactant ◽  
Micellar Systems ◽  
Aggregation Numbers ◽  
Ethoxylated Alcohols

The micelle formation process for a zwitterionic surfactant, N-dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate (ZW3-12), has been investigated in a series of mixed solvents consisting of different concentrations of ethoxylated alcohols and polymers. The critical micelle concentrations (cmc values) of the aggregates were determined by fluorescence spectroscopy, and the surfactant aggregation numbers were obtained from luminescence probing experiments. The cmc values for ZW3-12 changed very little in the presence of increasing amounts of poly(ethyleneoxide) (PEO) in the mixed solvent. In the case of the ethoxylated alcohol – ZW3-12 systems, the cmc values and aggregation numbers decreased systematically with increasing alcohol concentration. However, the cmc values of the mixed micelles showed little dependence on the number of ethylene oxide (EO) groups at constant alcohol concentration. These results are compared with the well-studied sodium dodecylsulfate – ethoxylated alcohol, and dodecyltrimethylammonium bromide – ethoxylated alcohol mixed micellar systems and to SDS–PEO systems and are discussed in terms of the contribution of the EO groups to the hydrophobic interactions. Key words: zwitterionic surfactant, alcohols, mixed micelles, luminescence probing.

Impacts of polyols and temperature on the micellization, interaction and thermodynamics behavior of the mixture of tetradecyltrimethylammonium bromide and polyvinyl alcohol

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Sharmin Sultana ◽  
Abdullah Al Mamun ◽  
Shahina Aktar ◽  
Shamim Mahbub ◽  
Kareem Yusuf ◽  
...  
Keyword(s):  
Thermodynamic Properties ◽  
Polyvinyl Alcohol ◽  
Hydrophobic Interactions ◽  
Specific Conductivity ◽  
Mixed Solvents ◽  
Conductivity Measurement ◽  
Micelle Formation ◽  
Tetradecyltrimethylammonium Bromide ◽  
Delta G ◽  
Free Energy Of Micellization

Abstract Herein, the aggregation manner of the mixture of polyvinyl alcohol (PVA) and tetradecyltrimethylammonium bromide (TTAB) was performed in polyols (glucose, maltose and galactose) media over 300.55–320.55 K temperatures range with 5 K interval through conductivity measurement method. The micelle formation of TTAB + PVA mixture was identified by the assessment of critical micelle concentration (CMC) from the plots of specific conductivity (κ) versus TTAB concentration. The degree of micelle ionization (α), the extent of bound counter ions (β) as well as thermodynamic properties ( Δ G m 0 ${\Delta}{G}_{m}^{0}$ , Δ H m 0 ${\Delta}{H}_{m}^{0}$ and Δ S m 0 ${\Delta}{S}_{m}^{0}$ ) of TTAB + PVA systems have been estimated. The CMC values reveal that the micelle formation of TTAB + PVA mixture experience an enhancement in the manifestation of polyols. The values of free energy of micellization ( Δ G m 0 ${\Delta}{G}_{m}^{0}$ ) are negative for the TTAB + PVA system in aqueous polyols media, suggesting a spontaneous aggregation phenomenon. The Δ H m 0 ${\Delta}{H}_{m}^{0}$ and Δ S m 0 ${\Delta}{S}_{m}^{0}$ values of TTAB + PVA systems direct that the PVA molecule interacts with TTAB through the exothermic, ion-dipole, and hydrophobic interactions. The thermodynamic properties of transfer were also determined for the move of TTAB + PVA mixture from H2O to water + polyols mixed solvents. The values of compensation temperature (T c) and intrinsic enthalpy gain ( Δ H m 0 , ∗ ${\Delta}{H}_{m}^{0,\ast }$ ) were evaluated and discussed for the studied system.

Rate enhancements for the nickel(II)–PADA complexation in mixed anionic micelles

1983 ◽  
Vol 61 (7) ◽  
pp. 1594-1597 ◽  
Author(s):  
Paul D. I. Fletcher ◽  
Joanne R. Hicks ◽  
Vincent C. Reinsborough
Keyword(s):  
Kinetic Analysis ◽  
Mixed Micelle ◽  
Mixed Micelles ◽  
Sodium Dodecylsulfate ◽  
Electrostatic Forces ◽  
Rate Enhancement ◽  
The Third ◽  
Micellar Systems ◽  
Sodium Decylsulfate ◽  
Anionic Micelles

Rate enhancements for the [Formula: see text] and pyridine-2-azo-p-dimethylaniline (PADA) reaction have been obtained in four simple equimolar binary micellar systems: sodium dodecylsulfate – sodium decylsulfate, sodium dodecylsulfate – sodium octylsulfate, sodium octylsulfate – sodium hexylsulfate, and sodium octylsulfate – sodium octanesulfonate. The rate enhancement curves were similar to those obtained for pure surfactants and were consistent with a 1:1 mixed micelle except for the third system where the micelle was richer in sodium octylsulfate. The kinetic analysis revealed no dramatic changes in hydrophobic or electrostatic forces on forming the mixed micelles

scholarly journals The Additive Influence of Propane-1,2-Diol on SDS Micellar Structure and Properties

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3773
Author(s):  
Martina Gudelj ◽  
Paola Šurina ◽  
Lucija Jurko ◽  
Ante Prkić ◽  
Perica Bošković
Keyword(s):  
Mixed Solvents ◽  
Sodium Dodecyl ◽  
Shielding Effect ◽  
Bulk Solution ◽  
Structure And Properties ◽  
Micellar Structure ◽  
Related Substances ◽  
Micellar Systems ◽  
Small Change ◽  
Additive Influence

Micellar systems are colloids with significant properties for pharmaceutical and food applications. They can be used to formulate thermodynamically stable mixtures to solubilize hydrophobic food-related substances. Furthermore, micellar formation is a complex process in which a variety of intermolecular interactions determine the course of formation and most important are the hydrophobic and hydrophilic interactions between surfactant–solvent and solvent–solvent. Glycols are organic compounds that belong to the group of alcohols. Among them, propane-1,2-diol (PG) is a substance commonly used as a food additive or ingredient in many cosmetic and hygiene products. The nature of the additive influences the micellar structure and properties of sodium dodecyl sulfate (SDS). When increasing the mass fraction of propane-1,2-diol in binary mixtures, the c.m.c. values decrease because propane-1,2-diol is a polar solvent, which gives it the ability to form hydrogen bonds, decreasing the cohesivity of water and reducing the dielectric constant of the aqueous phase. The values of ΔGm0 are negative in all mixed solvents according to the reduction in solvophobic interactions and increase in electrostatic interaction. With the rising concentration of cosolvent, the equilibrium between cosolvent in bulk solution and in the formed micelles is on the side of micelles, leading to the formation of micelles at a lower concentration with a small change in micellar size. According to the 1H NMR, with the addition of propylene glycol, there is a slight shift of SDS peaks towards lower ppm regions in comparison to the D2O peak. The shift is more evident with the increase in the amount of added propane-1,2-diol in comparison to the NMR spectra of pure SDS. Addition of propane-1,2-diol causes the upfield shift of the protons associated with hydrophilic groups, causing the shielding effect. This signifies that the alcohol is linked with the polar head groups of SDS due to its proximity to the SDS molecules.

Interaction of sulphone based reactive dyes with cationic surfactant: a spectroscopic and conductometric study

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Misbah Iram ◽  
Hamadia Sultana ◽  
Muhammad Usman ◽  
Bazgha Ahmad ◽  
Nadia Akram ◽  
...  
Keyword(s):  
Strong Interaction ◽  
Cetyltrimethylammonium Bromide ◽  
Hydrophobic Interactions ◽  
Reactive Dyes ◽  
Micellar System ◽  
Palisade Layer ◽  
Micellar Systems ◽  
Gibbs Energies ◽  
Electrostatic And Hydrophobic Interactions ◽  
Conductometric Study

Abstract Interaction of sulphone based reactive dyes, designated as dye-1 and dye-2, with cationic micellar system of cetyltrimethylammonium bromide (CTAB), has been investigated by spectroscopic and conductometeric measurements. Efficiency of the selected micellar systems is assessed by the values of binding constant (K b ), partition coefficient (K x ) and respective Gibbs energies. Critical micelle concentration (CMC) of surfactant, electrostatic and hydrophobic interactions as well as polarity of the medium plays significant role in this phenomenon. The negative values of Gibbs energies of binding (∆G b ) and partition (∆G p ) predicts the feasibility and spontaneity of respective processes. Similarly negative values of ∆G m and ∆H m and positive values of ∆S m , calculated from conductometeric data, further, revealed the exothermicity, spontaneity and, thus, stability of system. The results, herein, have disclosed the strong interaction between dye and surfactant molecules. The dye-2 has been observed to be solubilized to greater extent, as compared to dye 1, due to strong interaction ith hydrophiles of CTAB and accommodation of its molecules in palisade layer of micelle closer to the micelle/water interface.

Hydrophobic interactions in human casein micelle formation: β-casein aggregation

1989 ◽  
Vol 56 (3) ◽  
pp. 427-433 ◽  
Author(s):  
Charles W. Slattery ◽  
Satish M. Sood ◽  
Pat Chang
Keyword(s):  
Light Scattering ◽  
Conformational Transition ◽  
Hydrophobic Interactions ◽  
Micelle Formation ◽  
Tryptophan Fluorescence ◽  
Phosphate Esters ◽  
Casein Micelle ◽  
Protein Association ◽  
P Protein ◽  
Micelle Size

SummaryThe association of non-phosphorylated (0-P) and fully phosphorylated (5-P) human β-caseins was studied by fluorescence spectroscopy and laser light scattering. The tryptophan fluorescence intensity (FI) level increased between 20 and 35 °C, indicating a change in the environment of that residue. A similar transition occurred when ANS was used as a probe. Transition temperatures were slightly lower in 10 mM-CaCl2 but were not affected by an equivalent increase in ionic strength caused by NaCl. The magnitude of the FI change was less for the 5-P than the 0-P protein but was increased for both by CaCl2 addition. These FI data were characteristic of a conformational change and this was supported by fluorescence polarization which indicated that with CaCl2, tryptophan and ANS mobility increased at the transition temperature even though the extent of protein association also increased. Light scattering suggested that protein association proeeeded with the primary formation of submicellar aggregates containing 20–30 monomers which then associated further to form particles of minimum micelle size (12–15 submicelles), and eventually larger. The temperature of precipitation of the 5-P form in the presence of CaCl2 was lower than the conformational transition and suggested that both hydrophobic interactions and Ca bridges between phosphate esters on adjacent molecules are important in micelle formation.

scholarly journals Prospects for the use of mixed micellar structures as a template in synthesis of MCM-41-type silicas

2021 ◽  
pp. 79-89
Author(s):  
N.V. Roik ◽  
◽  
L.O. Belyakova ◽  
М.О. Dziazko
Keyword(s):  
Azo Dye ◽  
Cetyltrimethylammonium Bromide ◽  
Mixed Micelles ◽  
Hydrophobic Interactions ◽  
Sol Gel ◽  
Standard Free Energy ◽  
Reaction Medium ◽  
Total Pore Volume ◽  
Methyl Red ◽  
Sol Gel Synthesis

Formation of mixed micelles assisted by cetyltrimethylammonium bromide and methyl red was studied by means of conductometric and spectrophotometric methods. It follows from the analysis of conductometric dependences that the addition of azo dye leads to a decrease in critical micelle concentration of a long-chain quaternary ammonium salt. The respective thermodynamic parameters were calculated. The process of mixed micelles formation was stated to be spontaneous and the solubilization of azo dye by micelles of cetyltrimethylammonium bromide is profitable in terms of energy and accompanied by an increase in degrees of freedom of the system. Based on the data of spectrophotometric study of methyl red solutions in the presence of cetyltrimethylammonium bromide, the values of stability constant, partition coefficient and change in the standard free energy of methyl red distribution between aqueous and micellar medium were calculated. It was found that electrostatic and hydrophobic interactions arising between azo dye and cetyltrimethylammonium bromide molecules cause the orientation of methyl red from the shell towards the center of the micelles. It was shown that mixed micelles can be used as a template in sol-gel synthesis of mesoporous aminosilica of MSM-41 type. The results of low-temperature nitrogen adsorption-desorption and X-ray analysis revealed that the introduction of methyl red as a part of mixed micelles into the reaction medium of sol-gel synthesis causes substantial increase in specific surface area and total pore volume, noticeable reduction of pore diameter, thereby contributing to the formation of silica material with a pronounced long-range ordered mesoporous structure.

scholarly journals Molecular Interactions in Binary Surfactant Solutions: Effect of pH

2019 ◽  
Vol 64 (4) ◽  
pp. 437-445
Author(s):  
Olga Kochkodan ◽  
Victor Maksin ◽  
Nadiya Antraptseva ◽  
Tetyana Semenenko
Keyword(s):  
Molecular Interactions ◽  
Mixed Micelles ◽  
Ph Value ◽  
Chemical Properties ◽  
Micelle Formation ◽  
Bulk Solution ◽  
Surfactant Mixtures ◽  
Solution Ph ◽  
Solution Interface ◽  
Adsorption Layers

By using surface tension and conductivity measurements, the colloid-chemical properties of the mixtures of cationic hexadecylpyridinium bromide with nonionic Triton X-100 surfactants were investigated both in the bulk solution and at air/solution interface at different pH values. The composition of mixed micelles and adsorption layers, parameters of molecular interactions in mixed micelles βm and adsorption layers βσ, as well as standard free energies of micelle formation ΔG0mic and adsorption ΔG0ads were calculated. It was found that molecules of the nonionic surfactant presumably dominate in the mixed micelles and adsorption layers. It was shown that βm and βσ have negative values, which indicate the strengthening of intermolecular interactions in the mixed micelles and adsorption layers. Based on the data obtained, it was suggested that ion-dipole interactions are involved in the formation of intermolecular structures between nonionic and cationic surfactants in aqueous solution and at the air-solution interface. It was shown that βm, βσ as well as ΔG0mic and ΔG0ads parameter depends on the solution pH value. The complex interplay of ion-dipole, protonation and chelation processes, which occur in the surfactant mixtures at different pH and affect the strength of intermolecular interaction, should be taken into account for data analysis.

scholarly journals Solvation in pure and mixed solvents: Some recent developments

2007 ◽  
Vol 79 (6) ◽  
pp. 1135-1151 ◽  
Author(s):  
Omar A. El Seoud
Keyword(s):  
Hydrogen Bonding ◽  
Hydrophobic Interactions ◽  
Preferential Solvation ◽  
Mixed Solvents ◽  
Effect Of Temperature ◽  
Binary Solvent ◽  
Solvent Mixtures ◽  
Dispersion Interactions ◽  
Binary Solvent Mixtures ◽  
Recent Developments

The effect of solvents on the spectra, absorption, or emission of substances is called solvatochromism; it is due to solute/solvent nonspecific and specific interactions, including dipole/dipole, dipole-induced/dipole, dispersion interactions, and hydrogen bonding. Thermo-solvatochromism refers to the effect of temperature on solvatochromism. The molecular structure of certain substances, polarity probes, make them particularly sensitive to these interactions; their solutions in different solvents have distinct and vivid colors. The study of both phenomena sheds light on the relative importance of the solvation mechanisms. This account focuses on recent developments in solvation in pure and binary solvent mixtures. The former has been quantitatively analyzed in terms of a multiparameter equation, modified to include the lipophilicity of the solvent. Solvation in binary solvent mixtures is complex because of the phenomenon of "preferential solvation" of the probe by one component of the mixture. A recently introduced solvent exchange model allows calculation of the composition of the probe solvation shell, relative to that of bulk medium. This model is based on the presence of the organic solvent (S), water (W), and a 1:1 hydrogen-bonded species (S-W). Solvation by the latter is more efficient than by its precursor solvents, due to probe/solvent hydrogen-bonding and hydrophobic interactions. Dimethylsulfoxide (DMSO) is an exception, because the strong DMSO/W interactions probably deactivate the latter species toward solvation. The relevance of the results obtained to kinetics of reactions is briefly discussed by addressing temperature-induced desolvation of the species involved (reactants and activated complexes) and the complex dependence of kinetic data (observed rate constants and activation parameters) in binary solvent mixtures on medium composition.

Influence of taurocholate, taurochenodeoxycholate, and taurodehydrocholate on sulfobromophthalein transport into bile.

1979 ◽  
Vol 236 (1) ◽  
pp. E10
Author(s):  
S Binet ◽  
Y Delage ◽  
S Erlinger
Keyword(s):  
Bile Salts ◽  
Mixed Micelle ◽  
Mixed Micelles ◽  
Important Determinant ◽  
Micelle Formation ◽  
Similar Increase ◽  
Mixed Micelle Formation ◽  
Series Of Experiments

To test the hypothesis that incorporation of sulfobromophthalein (BSP) into mixed micelles could account for the increase in its biliary transport maximum (Tmax) by bile salts, we have compared in hamsters the influence on BSP Tmax of taurocholate and taurochenodeoxycholate (two micelle-forming physiological bile salts) to that of taurodehydrocholate, a bile salt which, in vitro, does not form micelles. In a first series of experiments, it was observed that taurocholate and taurochenodeoxycholate increased the secretion of phospholipid (40 and 53%, respectively), and cholesterol (50 and 110%, respectively), whereas taurodehydrocholate decreased the secretion of phospholipid (-31%) and cholesterol (-43%). This result suggests that, in vivo, taurodehydrocholate or its metabolites do not form mixed micelles. In a second series of experiments, it was seen that the three bile salts induced a similar increase in BSP Tmax (63% with taurocholate, 52% with taurochenodeoxycholate, and 51% with taurodehydrocholate). These results provide circumstantial evidence for the hypothesis that mixed micelle formation is not an important determinant of maximal BSP secretion into bile.

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