Effect of imidazolium-based ionic liquids on the aggregation behavior of twin-tailed cationic gemini surfactant in aqueous solution

Micellization behavior of the twin-tailed surfactants can be modulated by the addition of various modifiers. Ionic liquids (ILs) are one of them and are documented here. The beauty of these environmentally benign neoteric molecules lies in their structural versatility. Here, we have investigated the effect of three ILs: 1-butyl-3-methylimidazolium bromide ([C₄mim][Br]), 1-hexyl-3-methylimidazolium bromide ([C₆mim][Br]), and 1-octyl-3-methylimidazolium bromide ([C₈mim][Br]) on the aggregation and surface adsorption behavior of cationic gemini surfactant, bis(hexadecyldimethyl ammonium)propane dibromide (16-3-16) through experimentally measured electrical conductivities, surface tensions, and by spectral methods (UV-vis absorbance and fluorescence measurements). The main focus of the study is to observe the effect of added ILs on the critical micelle concentration (cmc), various surface parameters, aggregation number, and size of the aggregates of gemini surfactant. The results show that the more hydrophobic ILs, that is, [C₆mim][Br] and [C₈mim][Br] behave as electrolyte at lower concentration and cosurfactant at higher concentration, whereas moderately hydrophobic IL [C₄mim][Br] acts as an electrolyte at all concentration ranges studied. The modulating effects of ILs were also compared with conventional electrolyte (NaBr) at similar conditions.     

Aggregation and thermodynamic properties of ionic liquid-type gemini imidazolium surfactants with different spacer length

The aggregation behavior and thermodynamic properties of micellization for the ionic liquid-type gemini imidazolium surfactants with different spacer length ([C₁₂–s–C₁₂im]Br₂, s = 2, 4, 6) have been investigated by means of surface tension, electrical conductivity, dynamic light scattering and fluorescence measurements. The values of cmc, γ _cmc, Γ _max, A _min, π _cmc, pc₂₀ and cmc/pc₂₀ suggest that the shorter the spacer, the higher the surface activity of [C₁₂–s–C₁₂im]Br₂ is. The cmc and γ _cmc values are decreased significantly in the presence of sodium halides, and the values decrease in the order NaCl < NaBr < NaI. The thermodynamic parameters of micellization (, , ) indicate that the micellization of [C₁₂–2–C₁₂im]Br₂ and [C₁₂–4–C₁₂im]Br₂ is entropy-driven, whereas aggregation of [C₁₂–6–C₁₂im]Br₂ is enthalpy-driven at lower temperature but entropy-driven at higher temperature. Finally, the fluorescence measurements show that the micropolarity of micelles increases but the aggregation numbers decrease with increasing the spacer length of [C₁₂–s–C₁₂im]Br₂.     

Synthesis and monolayer film of a series of new twin-tailed gemini cationic surfactants at the air/water interface

A series of new dimeric surfactants, twin-tailed gemini surfactants, 2(12)-s-2(12), were successfully prepared and characterized, and their monolayer films investigated by the measurement of surface pressure-area (π-A) and surface pressure-time (π-t) isotherms at the air/water interface by a Langmuir film balance. Compared to their monomeric counterparts, their collapse pressure (γ_collapse) is smaller, whilst all the molecular area parameters are larger. The limited area (A_limited) and the initial area (A_initial) of these twin-tailed gemini surfactants change with increasing spacer length s, and the surface pressure decreases with increasing time. It was also found that the higher the initial surface pressure, the larger the attenuation.      

Micellization and mixed micellization of cationic gemini (dimeric) surfactants and cationic conventional (monomeric) surfactants: Conductometric,dye solubilization,and surface tension studies

In the present study, we have investigated the self-association, mixed micellization, and thermodynamic studies of a cationic gemini (dimeric) surfactant, hexanediyl-1,6-bis(dimethylcetylammonium bromide (16-6-16)) and a cationic conventional (monomeric) surfactant, cetyltrimethylammonium bromide (CTAB). The critical micelle concentration (CMC) of pure (16-6-16 and CTAB) and mixed (16-6-16+CTAB) surfactants was measured by electrical conductivity, dye solubilization, and surface tension measurements. The surface properties (viz., C₂₀ (the surfactant concentration required to reduce the surface tension by 20 mN/m), Π_CMC (the surface pressure at the CMC), Γ_max (maximum surface excess concentration at the air/water interface), A_min (the minimum area per surfactant molecule at the air/water interface), etc.) of micellar (16-6-16 or CTAB) and mixed micellar (16-6-16+CTAB) surfactant systems were evaluated. The thermodynamic parameters of the micellar (16-6-16 and CTAB) and mixed micellar (16-6-16+CTAB) surfactant systems were also evaluated.     

双子表面活性剂及其保护的纳米金作为缓冲添加剂用于毛细管电泳蛋白质分离

报道了使用阳离子双子表面活性剂作为毛细管电泳的缓冲添加剂用于同时分离酸性和碱性蛋白质.在酸性的缓冲条件下,只需要使用低浓度的阳离子双子表面活性剂（0.1mmol/L18-s-18）作为缓冲液的添加剂,就可以有效地抑制酸性和碱性蛋白质在毛细管壁的吸附,从而得到高效的蛋白质分离.实验表明,较小的胶束尺寸（如s=5～8）比大的胶束尺寸（如s〈4或〉10）能更有效地抑制酸性蛋白质的吸附.改变双子表面活性剂的中间基的长度能够对蛋白质的电泳淌度进行一定的调节,从而对分离的选择性进行一定的优化.在最优的实验条件下,蛋白质迁移时间的日内和日间标准偏差（RSD）分别小于0.8%和2.2%,回收率为79%到100.4%.另外,还考察了双子表面活性剂保护的金纳米颗粒用作毛细管电泳缓冲添加剂在蛋白质分离中的应用.实验表明,在缓冲液中加入纳米金能够缩短分析时间,并能小幅度地提高分离效率.最后,使用该方法分析了一系列复杂生物样品,包括血浆、红细胞和鸡蛋清样品,均得到了满意的结果.     

Separation of acidic and basic proteins by capillary electrophoresis using gemini surfactants and gemini-capped nanoparticles as buffer additives

This paper demonstrated simultaneous separation of acidic and basic proteins using cationic gemini surfactants as buffer additives in capillary electrophoresis. We showed that even at a low concentration (0.1 mmol·L-1) of alkanediyl-α,ω-bis(dimethyloctadecylammonium bromide) (18-s-18), the wall adsorption of both acidic and basic proteins could be effectively suppressed under acidic conditions. Smaller micelle size (e.g., s=5-8) is more effective for the separation of acidic proteins than larger micelle siz...     

Mercury extraction by ionic liquids: temperature and alkyl chain length effect

The preliminary results described here show the complete transfer of Hg(II) ions, in the absence of a chelating agent in 1-alkyl-3-methylimidazolium hexafluorophosphate ionic liquids; the lag time required to gain the quantitative metal ion partition turned out to be strongly dependent both on alkyl chain length on the imidazolium ring and on the working temperature.     

Study on the adsorption and aggregation of dilute gemini surfactant solutions

As a function of temperature in aqueous solutions, the adsorption and aggregation of N,N’-bis (tetradecyl dimethyl)-1,2-dibromide-ethanediyl ammonium salt (GS14-2-14) and N,N’-bis (hexadecyl dimethyl)-1,2-dibromide-ethanediyl ammonium salt (GS16-2-16), were researched with drop-volume technique and conductometry, respectively. The results of surface tension measurements, which were analyzed by originally developed thermodynamic equations, illustrate that GS14-2-14 has a better surface activity and arranges more tightly in the adsorbed film than GS16-2-16. The data of conductivity were used to find critical micelle concentration (cmc) and counterion binding degree of micelle (β). Thermodynamic parameters of micellization were also obtained from the temperature dependence of cmc values. From the study, it is discovered that the micellization process is spontaneous and exothermic in nature and it is mainly driven by entropy.     

Effect of (chloride salt) electrolytes on the mixed micellization of (equimolar) a cationic gemini (dimeric) surfactant and a cationic conventional (monomeric) surfactant

Herein we report the effect of (chloride salt) electrolytes on the mixed micellization of (equimolar) a cationic gemini (dimeric) surfactant, hexanediyl-1,6-bis(dimethylcetylammonium bromide) (16-6-16), and a cationic conventional (monomeric) surfactant, cetyltrimethylammonium bromide (CTAB) in aqueous solutions. In absence and presence of (chloride salt) MCl (where M?Li, Na, and K) electrolytes, the critical micelle concentration (CMC) of mixed (16-6-16 + CTAB) surfactants was measured by surface tension measurements. With increasing the concentration of electrolyte, the CMCs were increasing. The surface properties and the thermodynamic parameters of the mixed micellar systems were also evaluated. From these evaluated thermodynamic parameters, it was found that in presence of electrolyte the stability of the mixed micellar system is more.     

Kinetics of the Esterification Reaction Catalyzed by Lipase in W／O Microemulsions of Alkyl Polyglucoside

A novel kinetic mechanism of esterification reaction of 1-hexanoic acid with 1-butanol,catalyzed by lipase, was studied in water-in-oil microemulsions. The microemulsions were formed by alkyl polyglucoside C10G1.54/1-butanol/cyclohexane/phosphate buffer solution. The restult shows that when the ratio of mol concentration of 1-butanol to 1-hexanoic acid is about 3.0,the initial rate V0 get the maximum values. This phenomenon was explained by the modified fishlike phase diagrams.     

FT-IR studies on the conformation and effective head-group area of AOT molecules in W/O microemulsions

Using Fourier transform infrared(FT-IR) spectroscopy technique, the carbonyl stretching vibration bands of AOT in sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/isooctane/water reverse (W/O) microemulsions system have been investigated by least square curve fitting. The results indicate that an asymmetric adsorbed peak of carbonyl stretching vibration of AOT molecule is situated in (1739 ± 1) and (1725 ± 2) cm-1. The two peaks correspond to different carbonyls in gauche conformation and trans conformation of AOT molecules, respectively. With different water contents (W0), the variations of peak intensity ratio (/= l1739/l1725) reflect the change of the ratio for the two conformation populations and the variations of the effective head-group area of AOT molecule have relations to the ratio of two conformation populations.     

Strong effect of NaBr on self-assembly of quaternary ammonium gemini surfactants at air/water interface and in aqueous solution studied by surface tension and fluorescence techniques

The effects of NaBr on the adsorption of alkanediyl-bis-(dimethyl dodecyl- ammonium bromide) (referred to as C₁₂-s-C₁₂ 2Br) at the air/water interface and on the micellization in the solution have been investigated by surface tension and fluorescence techniques. The results showed that the addition of NaBr greatly enhances their efficiency and effectiveness in surface tension reduction as well as the ability of micellization, even induces strong premicellar aggregation before the cmc. These were attributed to the unique molecular structure of gemini surfactant, where the flexible polymethylene chain was the spacer linking the two quaternary ammonium heads. By a short spacer, the charges of the two quaternary ammonium head groups are concentrated. Even for a long spacer (s = 12), since it is bent toward the alkyl tails, the similar effect is also produced. This results in the high sensitivity of their ionic head groups to salt. Besides, the addition of salt also effectively promotes the hydrophobic interaction between the alkyl tails of gemini surfactants. The addition of NaBr strongly promotes the adsorption of quaternary ammonium gemini surfactants C₁₂-s-C₁₂ 2Br at the air/water interface and the micellization in the solution.     

Salt effects on the protonation of imidazole in aqueous solution at different ionic strengths: A tentative explanation by a complex formation model

Imidazole protonation constants were determined potentiometrically, using a (H⁺)-glass electrode, in LiCl, NaCl, KCl, CaCl₂, MgCl₂, tetramethylammonium (Me₄N-) iodide and chloride, Et₄N-, Pr₄N- and Bu₄N-iodides. Salt effects were tentatively explained by assuming that complexes [H(Im)X]^o (Im = imidazole, X^–=Cl^– or I^–), [M(Im)]²⁺ (M²⁺=Mg²⁺ or Ca²⁺) and [A(Im)]⁺ (A⁺ = tetraalkylammonium cation) were formed in solution. Calcium(II)-selective electrode measurements confirmed our hypothesis about the formation of the Ca²⁺-imidazole complex. The reliability of the complex formation model is discussed on the basis of its self consistency and in light of previous results.     

Blockcopolymers in microemulsions differential heats of solution and shift of the percolation temperature in W/O microemulsions

Solutions of blockcopolymers (POE-b-PI-b-POE) in fluids of interacting aqueous nanodroplets (W/O microemulsions) are studied. The interaction strength between the (pseudo) two components is measured by the shift of the percolation temperature relative to that of the pure microemulsion. A quantitative measure of the interaction, the differential heat of solution, is thermodynamically related to the slopes of the equilibrium temperature of the system with varying monomeric nanodroplet concentration and the experimental percolation line in the presence of copolymer.     

DPD Simulation on the Transformation and Stability of O/W and W/O Microemulsions

The dissipative particle dynamics simulation method is adopted to investigate the microemulsion systems prepared with surfactant (H1T1), oil (O) and water (W), which are expressed by coarse-grained models. Two topologies of O/W and W/O microemulsions are simulated with various oil and water ratios. Inverse W/O microemulsion transform to O/W microemulsion by decreasing the ratio of oil-water from 3:1 to 1:3. The stability of O/W and W/O microemulsion is controlled by shear rate, inorganic salt and the temperature, and the corresponding results are analyzed by the translucent three-dimensional structure, the mean interfacial tension and end-to-end distance of H1T1. The results show that W/O microemulsion is more stable than O/W microemulsion to resist higher inorganic salt concentration, shear rate and temperature. This investigation provides a powerful tool to predict the structure and the stability of various microemulsion systems, which is of great importance to developing new multifunctional microemulsions for multiple applications.     

Effects of additional salts on the interfacial tension of crude oil/zwitterionic gemini surfactant solutions

Zwitterionic gemini surfactants, which have the advantages of both zwitterionic and gemini surfactants, have been widely used in various disciplines. Sulfobetaine-type zwitterionic gemini surfactants consisting of 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (2C_nSb with 6, 8 and 10 carbon atoms) were evaluated for their interfacial activities at the water/crude oil interface. The 2C₁₀Sb molecules showed a remarkable ability to decrease the interface tension (IFT) of water/crude oil, and the degree of decrease was much greater than those in either zwitterionic or gemini surfactant systems by at least two orders of magnitude. Furthermore, the effects of salts (NaCl, CaCl₂, and MgCl₂) on the IFT of the 2C₁₀Sb system were thoroughly investigated. Interestingly, the delicate balance between the effects of additional cations and the intramolecular interactions of 2C₁₀Sb molecules played crucial roles in the interfacial arrangements of 2C₁₀Sb molecules, which were mainly dependent on the bonding abilities of the cations. Moreover, a zwitterionic surfactant and a cationic gemini surfactant were employed in control experiments to verify the proposed mechanisms.     

Molecularly imprinted SPE coupled with HPLC for the selective separation and enrichment of alkyl imidazolium ionic liquids in environmental water samples

A novel 1‐butyl‐3‐methylimidazolium chloride ionic liquid surface imprinted solid‐phase sorbent was synthesized. The as‐prepared material was characterized by SEM, Brunauer–Emmett–Teller surface area analysis and Fourier Transform IR measurements. Then its adsorption properties for alkyl imidazolium ionic liquids, including adsorption capacities, adsorption kinetics, and properties of selective separation and enrichment were studied in detail. It was shown that the ionic liquid surface imprinted polymer exhibited high selective recognition characteristics for the imidazolium chloride ionic liquids with short alkyl chains (C_nmimCl, n = 2, 4, 6, 8) and the adsorption equilibrium was achieved within 25 min. Various parameters were optimized for the 1‐butyl‐3‐methylimidazolium chloride ionic liquid surface imprinted polymer SPE column, such as flow rate, eluent solvent, selectivity, and reusability of the column. Then, the SPE column coupled with HPLC was used for the determination of alkyl imidazolium ionic liquids. Experimental results showed that the existence of their structural analogs and common concomitants in environmental matrices did not affect the enrichment of 1‐butyl‐3‐methyl imidazolium chloride ionic liquid. The average recoveries of 1‐butyl‐3‐methylimidazolium chloride ionic liquid in spiked water samples were in the range of 92.0–102.0% with the RSD lower than 5.8%.     

Preparation of hollow silica nanospheres in O/W microemulsion system by hydrothermal temperature changes

Hollow silica nanospheres with wrinkled or smooth surfaces were successfully fabricated through a hydrothermal method. In this method, oil-in-water microemulsion (composed of cyclohexane, water, ethanol, and cetyltrimethylammonium bromide), and polyvinylpyrrolidone were utilized as template and capping agent, respectively. In such a facile synthesis, we can well realize the morphological transformation of spheres with radially oriented mesochannels to hollow structures of silica nanoparticle only by regulating the hydrothermal temperature from 100 °C to 200 °C. Synthesized samples with different mesostructures were then used as supports to immobilize Candida rugosa lipase (CRL). The immobilized CRL was employed as a new biocatalyst for biodiesel production through the esterification of heptanoic acid with ethanol. The conversion ratio of heptanoic acid with ethanol catalyzed by the immobilized CRL was also evaluated. Results of this study suggest that the prepared samples have potential applications in biocatalysis.