Lyotropic Liquid Crystal Formed in Oleyl Polyoxyethylene Solutions by Adding Different Additives: NaDC,Tween 80, Alkyl Esters

Lyotropic liquid crystalline of oleylpolyoxyethylene(20)(AEO₂₀)/oil/water system was investigated at 25°C. The phase behavior, microstructure, and rheological properties of liquid crystalline were investigated by rheological techniques and polarizingoptical microscopy in the presence of various additives including Tween 80, sodium deoxycholate (NaDC), isoamylacetate, butyl acetate, isopropyl myristate. Diagrams show that cubic phase transforms to hexagonal phase when a shorter chain length oil is applied or NaDC or Tween 80 is added to the system.Flow experiments indicate the shear-thinning properties and a plastic behavior. The turning points of flow curves of the system AEO₂₀ and system AEO₂₀/NaDC were found. The dynamic modulus increase with increase in water content however the tendency is weaken by adding NaDC. Frequency dependence of experimental G ′ and G ′ were fitted using the multiple Maxwell model the cubic LLCs described by three relaxation times while hexagonal LLCs described by 5–8 elements. When AEO₂₀ mixes with Tween 80, the hexagonal have a monotonic decrease distribution of relaxation times without valleys.     

Inhibition Effect of N-(Pyridin-2-yl-Carbamothioyl) Benzamide on the Corrosion of C-Steel in Sulfuric Acid Solutions

N-(Pyridin-2-yl-carbamothioyl)benzamide (PCMB) was newly synthesized and tested as a corrosion inhibitor for C-steel in 0.5 M H₂SO₄ using chemical and electrochemical techniques. Polarization measurements showed that the synthesized compound acted as a mixed inhibitor. The inhibition efficiencies obtained from the different methods were in good agreement. The inhibitive action of this compound is discussed in terms of blocking the electrode surface by adsorption of the inhibitor according to the Langmuir isotherm. The effect of temperature on the corrosion behavior in the absence and presence of 2.5 × 10^?5 M of PCMB was studied (283–308 K). The associated activation energies (E _a) and the thermodynamic parameters (ΔH*, ΔS*, K _ads, ΔG°_ads) for the adsorption process were determined. The ΔG°_ads value is ?36.55 kJ/mol, which indicated that the adsorption mechanism of PCMB on C-steel in 0.5 M H₂SO₄ solution was combined between physisorption and chemisorption processes.     

Comparative Studies of Removal of Methyl Green and Basic Fuchsin from Wastewater by a Novel Magnetic Nanoparticles Mg-Ferrites

Adsorptions of methyl green (MG) and basic fuchsin (BF) by magnetic MgFe₂O₄ were compared in this study. Adsorption mechanism studies indicated that electrostatic interaction may play a main role for MG, but for BF, hydrogen-bond interaction may be more predominant. Kinetics data of both dyes conformed to the pseudo-second order model. The overall rate process was mainly governed by intraparticle diffusion. Comparative isotherm studies indicated that MG followed the Langmuir isotherm and BF followed the Freundlich isotherm. Thermodynamic parameters revealed that the adsorption process was endothermic (ΔH ⁰ > 0) for MG, but it was exothermic (ΔH ⁰ < 0) for BF.     

Comparison of the Rheological Behavior of Solutions and Formulated Oil-in-Water Emulsions Containing Carboxymethylcellulose (CMC)

In this study, it was aimed to compare the rheological properties of carboxymethylcellulose (CMC) in aqueous solutions and their corresponding emulsions containing 0.05, 0.1, 0.25, and 0.5% CMC in the aqueous phase. Samples with 0.05 and 0.1% CMC showed Newtonian behavior, but shear-thinning behavior was observed in CMC solutions and emulsions with increasing CMC concentrations to 0.25% and 0.5%. Rheological behavior of all samples were modeled by Power law (R ² = 0.986–197) and Casson models (R ² = 0.968–1). According to the Ostwald–de Waele model, the consistency index of all samples was increased and the flow behavior index decreased with increasing CMC concentration. Comparison of our data with four predicting models (Einstein, Larson, Pal, and Dougherty-Krieger equations) showed that the viscosity of continuous phase controls the viscosity of emulsions with high CMC concentrations and these models are not applicable for such situations. Addition of CMC increased the emulsion stability of O/W emulsions. This stability was increased with increasing CMC concentrations.     

Dielectric analysis on phase transition and micelle shape of polyoxyethylene trisiloxane surfactant in dilute aqueous solution

The cloudy Silwet L-77 aqueous solution on the concentration range from 0.5%to 50%was investigated by dielectric relaxation spectroscopy.The concentration dependence of phase microstructure was confirmed by means of analyzing the dielectric parameters of bulk solution.The relaxation behavior was assigned to the interfacial polarization between the micelle and the medium,and the relaxation distribution parameter was used to figure the shape transition from sphere to ellipsoid with the concentration increasing.The synchronous reduction of permittivity and conductivity indicated the formation of the lamellar phase. As compensation,the quantity of the surfactant liquid phase gradually decreased,whose shape constantly kept ellipsoidal.     

Membrane Permeability and Stability of Liposomes Suspended in Shear Flow

The 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) liposome has been characterized in its stability and membrane permeability to 5(6)-carboxyfluorescein (CF) in the shear flow generated in the cone-and-plate geometry. The CF-containing liposomes (CFLs) were 101–323 nm in the mean diameter D _P as measured with the dynamic light scattering (DLS) method. Adsorption of lipids to the cone-and-plate was observed, which clearly depended on the shear stress applied at the shear rate γ up to 1.5 × 10³ s^?1. The permeability of CFLs with D _P of 101 and 117 nm definitely increased at the maximum γ value where the adsorption was negligible. The permeability coefficient of CF at 40°C in the shear flow was 5.7 times larger than that in the static liquid system. The DLS measurements revealed that the size distribution of CFLs with D _P of 101–189 nm was practically unchanged under the shear stress even at 55°C. The results obtained show that the shear stress can permeabilize the CFL membranes with neither structural collapse nor coalescence.     

Surface and Structural Properties of Gold Nanoparticles and Their Biofunctionalized Derivatives in Aqueous Electrolytes Solution

Gold nanoparticles reduced by sodium citrate (d ～ 10 nm) and purchased gold colloid particles (d ～ 500 nm) were examined and compared. The properties of both gold particles and their biofunctionalized derivatives with L-cysteine and L-glutathione were studied in the presence of sodium nitrate. The structural investigations indicated an aggregated inner structure.

The isoelectric points of pure gold, citrate reduced gold, and functionalized gold were measured and compared. The low isoelectric point of pure gold/water interface was explained by considering the distribution and accumulation of H⁺ and OH^? ions within the interfacial water layer, being more pronounced for OH^? ions.      

Separation and Extraction of Uranium from Leach Liquor Containing Uranium and Molybdenum by Solvent Extraction with LIX 622N

The leach liquor (0.5 g/L Mo, 0.05 g/L U) obtained from the leaching process of molybdenum-uranium ore material was treated using solvent extraction to recover U(VI) by LIX 622N, which is a salicylaldoxime derivative. The influence of various basic variables such as pH, concentration of LIX 622N, temperature, different stripping reagents, phase ratio, and diluents was examined. Using 10% LIX 622N with the aqueous solution of equilibrium pH 6.0 and a phase ratio organic phase:aqueous phase (O:A) = 1:1, a two-stage McCabe-Thiele plot was constructed, which showed 99.9% of U extraction with no co-extraction of molybdenum. This was confirmed by a 6-cycle counter current simulation (CCS) study. The obtained data of temperature on the extraction of uranium showed that the extraction process is exothermic with enthalpy change of ?20.949 kJ mol^?1. The stripping of U(VI) was quantitative using 4 M H₂SO₄. The stable complex UO₂(HSO₄)R_org formed during extraction, which supports the cation exchange mechanism, and was confirmed by FTIR spectral analysis.