Role of solubilized water in the reverse ionic liquid microemulsion of 1-butyl-3-methylimidazolium tetrafluoroborate/TX-100/benzene

The ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4) can form nonaqueous microemulsions with benzene by the aid of nonionic surfactant TX-100. The effect of water on ionic liquid-in-oil (IL/O) microemulsions was studied, and it was shown that the addition of small amount of water to the IL microemulsion contributed to the stability of microemulsion and thus increased the amount of solubilized bmimBF4 in the microemulsion. The conductivity measurements also showed that the attractive interactions between IL microdroplets were weakened, that is, the IL/O microemulsion becomes more stable in the present of some water. Fourier transform IR was carried out to analyze the states of the added water, and the result showed that these water molecules mainly behaved as bound water and trapped water, indicating that the water molecules are located in the palisade layers of the IL/O microemulsion. Furthermore, 1H NMR and 19F NMR spectra suggested that the added water molecules built the hydrogen binding network of imidazolium cations and H2O, BF4- anion and H2O, and at the same time the electronegative oxygen atoms of the oxyethylene units of TX-100 and water in the palisade layers, which made the palisade layers more firm and thus increased the stability of the microemulsion. The study can help in further understanding the formation mechanism of microemulsions. In addition, the characteristic solubilization behavior of the added water can provide an aqueous interface film for hydrolysis reactions and therefore may be used as an ideal medium to prepare porous or hollow nanomaterials.     

The effect of water on the microstructure of 1-butyl-3-methylimidazolium tetrafluoroborate/TX-100/benzene ionic liquid microemulsions

The ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]) forms nonaqueous microemulsions with benzene with the aid of nonionic surfactant TX-100. The phase diagram of the ternary system was prepared, and the microstructures of the microemulsion were recognized. On the basis of the phase diagram, a series of ionic liquid-in-oil (IL/O) microemulsions were chosen and characterized by dynamic light scattering (DLS), which shows a similar swelling behavior to typical water-in-oil (W/O) microemulsions. The existence of IL pools in the IL/O microemulsion was confirmed by UV/Vis spectroscopic analysis with CoCl2 and methylene blue (MB) as the absorption probes. A constant polarity of the IL pool is observed, even if small amounts of water are added to the microemulsion, thus suggesting that the water molecules are solubilized in the polar outer shell of the microemulsion, as confirmed by FTIR spectra. 1H NMR spectroscopic analysis shows that these water molecules interact with the electronegative oxygen atoms of the oxyethylene (OE) units of TX-100 through hydrogen-bonding interactions, and the electronegative oxygen atoms of the water molecules attract the electropositive imidazolium rings of [bmim][BF4]. Hence, the water molecules are like a glue that stick the IL and OE units more tightly together and thus make the microemulsion system more stable. Considering the unique solubilization behavior of added water molecules, the IL/O microemulsion system may be used as a medium to prepare porous or hollow nanomaterials by hydrolysis reactions.     

Structural studies of 1-butyl-3-methylimidazolium tetrafluoroborate/TX-100/ p-xylene ionic liquid microemulsions.

The ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4) forms nonaqueous microemulsions with p-xylene, with the aid of the nonionic surfactant TX-100. The phase behavior of the ternary system is investigated, and three microregions of the microemulsions-ionic liquid-in-oil (IL/O), bicontinuous, and oil-in-ionic liquid (O/IL)-are identified by conductivity measurements, according to percolation theory. On the basis of a phase diagram, a series of IL/O microemulsions are chosen and characterized by dynamic light scattering (DLS). The size of aggregates increases on increasing the amount of added polar component (bmimBF(4)), which is a similar phenomenon to that observed for typical water-in-oil (W/O) microemulsions, suggesting the formation of IL/O microemulsions. The microstructural characteristics of the microemulsions are investigated by FTIR and 1H NMR spectroscopy. The results indicate that the interaction between the electronegative oxygen atoms of the oxyethylene (OE) units in TX-100 and the electropositive imidazolium ring may be the driving force for the solubilization of bmimBF4 into the core of the TX-100 aggregates. In addition, the micropolarity of the microemulsions is investigated by using methyl orange (MO) as a UV/Vis spectroscopic probe. A relatively constant polarity of the microemulsion droplets is obtained in the IL microemulsion. Finally, a plausible structure for the IL/O microemulsion is presented.     

Comparison of electrodeposition of silver in ionic liquid microemulsions

Both ionic liquid (IL) and water are typical green solvents and have high electric conductivity. The use of IL microemulsions as templates and media for electrochemical synthesis of nano-materials is attractive. In this work, water-in-ionic liquid (W/IL) microemulsion and ionic liquid-in-water (IL/W) microemulsion were prepared, in which hydrophobic ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate was used. The cyclic voltammetry (CV) behavior and electroplating in the W/IL and IL/W microemulsion systems containing silver nitrate were investigated for the first time. Both the CV curves exhibit the presence of reduction and oxidation peaks corresponding to the deposition and dissolution of silver from the two microemulsion systems. However, the CV obtained from IL/W microemulsion system exhibits a crossover, which is different from that obtained from W/IL microemulsion system. The electrodeposits obtained from W/IL microemulsion system are nano-granular, while those obtained from IL/W microemulsion system are planar. These results are attributed to the different microenvironments of the microemulsions.     

Decrease of droplet size of the reverse microemulsion 1-butyl-3-methylimidazolium tetrafluoroborate/Triton X-100/cyclohexane by addition of water

In the present contribution, results concerning the role of small amounts of water in the 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4)-in-cyclohexane ionic liquid (IL) reverse microemulsions are reported. Dynamic light scattering (DLS) revealed that the size of microemulsion droplets decreased remarkably with increasing water content although water is often used as a polar component to swell reverse microemulsions. It was thus deduced that the number of microemulsion droplets was increased which was confirmed by conductivity measurements. The states of dissolved water were investigated by Fourier transform IR (FTIR) spectroscopic analysis showing that water molecules mainly act as bound water. 1H NMR along with two-dimensional rotating frame nuclear Overhauser effect (NOE) experiments (ROESY) further revealed that water molecules were mainly located in the periphery of the polar core of the microemulsion droplets and behave like a chock being inserted in the palisade layer of the droplet. This increased the curvature of the surfactant film at the IL/cyclohexane interface and thus led to the decrease of the microemulsion droplet size. The order of surfactant molecules arranged in the interface film was increased and thus induced a loss of entropy. Isothermal titration calorimetry (ITC) indicated that an enthalpy increase compensates for the loss of entropy during the process of microstructural transition.     

Studies on the micropolarities of bmimBF4/TX-100/toluene ionic liquid microemulsions and their behaviors characterized by UV-visible spectroscopy

Ionic liquids (ILs), 1-butyl-3-methylimidazolium tetrafluoroborate (bmimBF4), were substituted for polar water and formed nonaqueous microemulsions with toluene by the aid of nonionic surfactant TX-100. The phase behavior of the ternary system was investigated, and microregions of bmimBF4-in-toluene (IL/O), bicontinuous, and toluene-in-bmimBF4 (O/IL) were identified by traditional electrical conductivity measurements. Dynamic light scattering (DLS) revealed the formation of the IL microemulsions. The micropolarities of the IL/O microemulsions were investigated by the UV-vis spectroscopy using the methyl orange (MO) and methylene blue (MB) as absorption probes. The results indicated that the polarity of the IL/O microemulsion increased only before the IL pools were formed, whereas a relatively fixed polar microenvironment was obtained in the IL pools of the microemulsions. Moreover, UV-vis spectroscopy has also shown that ionic salt compounds such as Ni(NO3)2, CoCl2, CuCl2, and biochemical reagent riboflavin could be solubilized into the IL/O microemulsion droplets, indicating that the IL/O microemulsions have potential application in the production of metallic or semiconductor nanomaterials, and in biological extractions or as solvents for enzymatic reactions. The IL/O microemulsions may have some expected effects due to the unique features of ILs and microemulsions.     

Second virial coefficient of bmimBF4/triton X-100/ cyclohexane ionic liquid microemulsion as investigated by microcalorimetry

The second virial coefficient of the ionic liquid (IL) microemulsion was obtained for the first time using microcalorimetry. The heat of dilution of the microemulsion solutions was measured by isothermal titration microcalorimetry (ITC), and the second virial coefficient was derived from the heat of dilution and the number density of the IL microemulsion solutions on the basis of a hard-sphere interaction potential assumption and as a function of the second-order polynomial. The validity of the second virial coefficient was confirmed by the percolation behavior of different ionic liquid microemulsion solutions of Triton X-100 in cyclohexane with or without added salts. The information obtained from the second virial coefficient shows that the interactions between ionic liquid microemulsion droplets are much stronger than those for traditional microemulsions, which may be attributed to the relatively larger size of the microemulsion droplets.     

Application of Multiple Linear Regression and Extended Principal-Component Analysis to Determination of the Acid Dissociation Constant of 7-Hydroxycoumarin in Water/AOT/Isooctane Reverse Micelles

The apparent pK(a) of dyes in water-in-oil microemulsions depends on the charge of the acid and base forms of the buffers present in the water pool. Extended principal-component analysis allows the precise determination of the apparent pK(a) and of the spectra of the acid and base forms of the dye. Combination with multiple linear regression increases the precision. The pK(a) of 7-hydroxycoumarin (umbelliferone) was spectrophotometrically measured in a water/AOT/isooctane microemulsion in the presence of a series of buffers carrying different charges at various different water/surfactant ratios. The spectra of the acid and base forms of the dye in the microemulsion are very similar to those in bulk water in the presence of Tris and ammonia. The presence of carbonate changes somewhat the spectrum of the acid form. Results are discussed taking into account the profile of the electrostatic potential drop in the water pool and the possible partition of umbelliferone between the aqueous core and the surfactant. The pK(a) values corrected for these effects are independent of w(0) and are close to the value of the pK(a) in bulk water. Copyright 2000 Academic Press.     

Microemulsions as reaction media for the synthesis of Pt nanoparticles

For the synthesis of Pt nanoparticles we used water-in-oil droplet microemulsions as templates. The focus was on the correlation between the size of the microemulsion droplets and that of the resulting Pt particles. To study this correlation in a systematic way, all particles were synthesized at the water emulsification failure boundaries where the microemulsion droplets are spherical and where their size can easily be tuned by the amount of added water. The metallic particles were synthesized by mixing two microemulsions one of which contains the metal salt H(2)PtCl(6) and the other the reducing agent NaBH(4). The size and structure of the microemulsion droplets was studied via small-angle X-ray scattering, while the Pt particles were characterized by high-resolution transmission electron microscopy in combination with energy-dispersive X-ray spectroscopy and selected area electron diffraction. The clear correlation between droplet and particle size was further supported by accompanying Monte Carlo simulations.     

Gelled polymerizable microemulsions. 2. Microstructure

Using bicontinuous microemulsions as templates opens a new field for the design of novel structures and thus novel materials, but has significant challenges due to the very small composition and temperature windows in which microemulsions are bicontinuous. In previous work we had shown that we can take a ternary base system (water-n-dodecane--C 13/15E 5), add monomer and cross-linker ( N-isopropylacrylamide and N, N'-methylenebisacrylamide) to the water phase, and add a gelator (12-hydroxyoctadecanoic acid) to the oil phase while remaining in the one-phase region of the phase diagram. It was also possible to allow the gelator to form an organogel by changing the temperature such that we crossed the sol--gel line, which fell within the one-phase region. In this work, we show conclusively that addition of the monomers and the gelator does not affect the microemulsion microstructure and that, even in the gelled state, the polymerizable microemulsion is indeed bicontinuous. 1H NMR self-diffusion, conductivity, and small-angle neutron scattering measurements all confirm the bicontinuous nature of the gelled polymerizable microemulsion.     

Tween80/BmimPF6/醇/甲苯体系的相行为

以环境友好型的Tween80为表面活性剂, 以醇(乙醇、正丁醇、正己醇、正辛醇、正癸醇和异戊醇)为助表面活性剂, 对离子液体1-丁基-3-甲基咪唑六氟磷酸盐(bmimPF6)和甲苯进行了微乳化实验, 绘制了不同条件下Tween80离子液体的微乳体系的拟三元相图, 考察了醇的种类、含量对单相微乳区的影响, 并用电导法研究了在乙醇为助表面活性剂情况下, 单相微乳区的结构转变. 结果表明, 当醇(异戊醇)固定时, 随着表面活性剂/醇的质量比增加, 单相微乳区的面积逐渐增大; 不同链长的直链醇对单相微乳区的面积影响与该醇在离子液体中的溶解情况有关, 单相微乳区的面积随着直链醇链长的增加而越小; 当乙醇作助表面活性剂时, 所得到的单相微乳区的面积最大, 且单相微乳区存在着O/IL(oil-in-ionic liquid)、双连续相和IL/O(ionic liquid-in-oil)三种微结构. 尤其对离子液体微乳体系的电导随油的含量的增加而最初增大的现象进行了解释, 这一现象是由于油主要起到减少离子液体中离子对或离子的积聚, 提高带电离子淌度的作用.     

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.     

Determination of the acid dissociation constant of bromocresol green and cresol red in water/AOT/isooctane reverse micelles by multiple linear regression and extended principal component analysis

The pKa of 3',3",5',5"tetrabromo-m-cresolsulfonephtalein (Bromocresol Green) and o-cresolsulphonephtalein (Cresol Red) was spectrophotometrically measured in a water/AOT/isooctane microemulsion in the presence of a series of buffers carrying different charges at different water/surfactant ratios. Extended Principal Component Analysis was used for a precise determination of the apparent pKa and of the spectra of the acid and base forms of the dye. The apparent pKa of dyes in water-in-oil microemulsions depends on the charge of the acid and base forms of the buffers present in the water pool. Combination with multiple linear regression increases the precision. Results are discussed taking into account the profile of the electrostatic potential in the water pool and the possible partition of the indicator between the aqueous core and the surfactant. The pKa corrected for these effects are independent of w0 and are close to the value of the pKa in bulk water. On the basis of a tentative hypothesis it is possible to calculate the true pKa of the buffer in the pool.     

Self-assembly in linker-modified microemulsions

Linker molecules are added to microemulsion systems to enhance the interaction between the surfactant and oil (lipophilic linkers) or water (hydrophilic linkers) phases. Previous results suggest that when lipophilic and hydrophilic linkers are combined they behave as a self-assembled surfactant at the oil/water interface. In this work we investigate this self-assembly phenomenon as a function of surfactant, linker and electrolyte concentration. We find that middle phase microemulsion appears at a specific concentration higher than the critical micelle concentration (CMC), which we denote as the critical middle phase microemulsion concentration (CmicroC). When the lipophilic linker dodecanol is added in equimolar ratio to the hydrophilic linker sodium mono- and dimethyl naphthalene sulfonate (SMDNS), the middle phase microemulsion did not appear until the surfactant sodium dihexyl sulfosuccinate (SDHS) concentration was larger than the CmicroC of the SDHS-alone system. Dodecanol is shown to segregate near the surfactant tails following a Langmuir-type adsorption process. This segregation is not affected by the electrolyte concentration but is significantly reduced when the surfactant (SDHS) concentration approaches the CmicroC. The data suggest that the self-assembly between hydrophilic and lipophilic linkers to form middle phase microemulsions is only possible if a minimum amount of surfactant is present.     

Study and Modeling of Metal Oxide Solubilization in (w/o) Microemulsions

Water-in-oil (w/o) microemulsions are very appealing reaction media due to their ability to provide huge surface of contact between water-soluble and oil-soluble reactants. Their application as reaction media, including the preparation of nanoparticles, is, however, limited to water soluble precursors. In this study, we present a first step scheme in a two-step process for the preparation of metal oxide nanoparticles starting from their water-insoluble metal oxide bulk powder. This step involves solubilizing the metal oxide in the water pools of the microemulsion with the aid of a solubilizing agent. The variables affecting the solubilizing capacity of iron and copper oxides, as examples of important metal oxides, in single HCl-containing AOT/water/isooctane microemulsions were investigated. The effect of the following variables on the solubilization capacity is reported, namely, mixing time, surfactant concentration, water to surfactant mole ratio (R), and the nominal concentration of HCl in the water pool. At 300-rpm, time-invariant concentration of the metals in the microemulsions was achieved in about 6 hours. These values were quoted as the solubilization capacity of the metal oxide at the corresponding conditions. Solubilization capacity increased linearly with the surfactant concentration and R, and portrait a power function with the nominal concentration of HCl in the water pool. A mathematical model previously derived to describe nanoparticle uptake by single microemulsion accurately accounted for the effect of the aforementioned variables on the solubilization capacity.     

A novel water-in-ionic liquid microemulsion and its interfacial effect on the activity of laccase

It is of great significance to develop an appropriate water-in-ionic liquid (W/IL) microemulsion suitable for the expression of the catalytic activity of a given enzyme. In this paper, the phase diagram of a new AOT/Triton X-100/H(2)O/[Bmim][PF(6)] pseudo ternary system is presented. With the aid of nonionic surfactant Triton X-100, AOT could be dissolved in hydrophobic ionic liquid [Bmim][PF(6)], forming a large single phase microemulsion region. The water-in-[Bmim][PF(6)] (W/IL) microemulsion domain was identified electrochemically by using K(3)Fe(CN)(6) as a probe. The existence of W/IL microemulsions was demonstrated spectrophotometrically by using CoCl(2) as a probe. New evidences from the FTIR spectroscopic study, which was first introduced to the W/IL microemulsion by substituting D(2)O for H(2)O to eliminate the spectral interference, demonstrated that there existed bulk water at larger ω(0) values (ω(0) was defined as the molar ratio of water to the total surfactant) in the W/IL microemulsion, which had remained unclear before. In addition to the inorganic salts, biomacromolecule laccase could be solubilized in the W/IL microemulsion. The laccase hosted in the microemulsion exhibited a catalytic activity and the activity could be regulated by the composition of the interfacial membrane.     

Research on electrochemical properties of nonaqueous ionic liquid microemulsions

The nonaqueous ionic liquid (IL) microemulsions composed of 1-butyl-3-methylimidazolium tetrafluoroborate, Triton X-100, and toluene were prepared and the electrochemical properties of the nonaqueous IL microemulsions were investigated in this paper. It is shown that characteristics of the nonaqueous IL microemulsions such as electrical conductivity, electrochemical window, and solubility are good, which indicate that the nonaqueous IL microemulsions can be used as electrolyte for electrochemical research. The electrochemical properties of the nonaqueous IL microemulsions were researched by cyclic voltammetry (CV) and electrochemical impedance spectroscopy methods using potassium ferricyanide as electroactive probe. It was found that the reversibility was better and the peak current densities of CV were higher for the [Fe(CN)₆]³⁻/[Fe(CN)₆]⁴⁻ electrode reaction in the nonaqueous IL microemulsions than those in IL. However, the electrochemical behavior of the probe in the nonaqueous IL microemulsions with different microenvironments (oil-in-IL, IL-in-oil, and bicontinuous) was different. The electrochemical property of the probe in the oil-in-IL microemulsion was the best, which was studied in detail.     

Preparation of metal nanoparticles in water-in-oil (w/o) microemulsions

The use of an inorganic phase in water-in-oil microemulsions has received considerable attention for preparing metal particles. This is a new technique, which allows preparation of ultrafine metal particles within the size range 5 nm相似文献   

Formation of Microemulsions in Aqueous NaCl/Sodium (3-Dodecanoyloxy-2-Hydroxy-Propyl) Succinate/Glycerol Mono(2-Ethylhexyl) Ether/Oil Systems

Sodium (3-dodecanoyloxy-2-hydroxy-propyl) succinate (SLGMS) forms microemulsions by mixing with cosurfactants such as glycerol mono(2-ethylhexyl) ether (MEH), although the combination with ordinary cosurfactant such as hexanol does not form a microemulsion of large solubilization. The middle-phase microemulsion coexists with excess water and oil (octane) phases at an optimum-mixing fraction of SLGMS and MEH in the presence of salt. The monomeric solubility of MEH in oil is low and MEH is mainly combined with SLGMS at an oil—water interface inside microemulsions. With decreasing salinity, the three-phase body shrinks and eventually disappears. The three-phase body may be terminated at a tricritical point, at which three phases simultaneously coexist. The effect of type of oil on the solubilization capacity of the microemulsions is also discussed.     

Comparison of O/W and IL/W Microemulsion Systems as Potential Carriers of Sparingly Soluble Celecoxib Drug

Active pharmaceutical ingredients with poor solubility in water and some organic solvents are a challenge in the pharmaceutical industry. To overcome this limitation, microemulsion systems are a choice to increase the solubility of a sparingly soluble active ingredient. The purpose of this study is to introduce and compare two types of oil-in-water (O/W) and ionic liquid-in-water (IL/W) microemulsions, which were formulated to increase the solubility of celecoxib as an active pharmaceutical ingredient. The proposed formulations are composed of the same nonionic surfactant/co-surfactant of Tween-80/transcutol®P, and different oil phases of isopropyl myristate, [BMIM][PF6] and [OMIM][PF6]. The pseudo-ternary phase diagrams for the microemulsion systems have been determined at a surfactant-to-co-surfactant mass ratio of 3:1 and 298.15 K. From the microemulsion region of the phase diagrams, four formulations was selected and their physico-chemical properties as density, viscosity, refractive index, electrical conductivity and surface tension were measured at 298.15 K. The solubilities of celecoxib in all selected formulations were also determined and compared. The results show considerable increases in solubility of the celecoxib in the ionic liquid-based microemulsion systems.