Dendritic Pattern Formation and Contact Line Forces during Dewetting of Dilute Polymer Solutions on a Hydrophobic Surface

The micro-scale morphology of the receding contact line of dilute polyethylene oxide solution drops (c ∼ 100 ppm) after impact and inertial spreading on a fluorinated hydrophobic surface is investigated. One can observe the formation of transient liquid filaments and dendritic structures that evolve into a bead-on-a-string structure similar to the well-known capillary breakup mechanism of dilute polymer solutions, which confirm the interaction between stetched polymer coils and the receding three-phase contact line. The estimation of the average polymer force per unit contact line lenght provides a quantitative explanation for the reduction of the contact line retraction velocity reduction observed experimentally.

Catalytic Production of Levulinic and Formic Acids from Fructose over Superacid ZrO2–SiO2–SnO2 Catalyst

Catalytic conversion of fructose to levulinic and formic acids over tin-containing superacid (H0 = −14.52) mixed oxide was studied. Mesoporous ZrO2–SiO2–SnO2 (Zr:Si:Sn = 1:2:0.4) was synthesized by the sol–gel method. The fructose transformation was carried out in a rotated autoclave at 160–190 °C for 1–5 h using a 20 wt.% aqueous solution. The results showed that doping ZrO2–SiO2 samples with Sn4+ ions improved both fructose conversion and selectivity toward levulinic and formic acids. Under optimal conditions of 180 °C, 3.5 h and fructose to catalyst weight ratio 20:1, levulinic and formic acids yields were 80% and 90%, respectively, at complete fructose conversion. At this, humic substances formed in the quantity of 10 wt.% based on the target products.

Microrheology to Understand the Viscosity Behavior of a Sophorolipid Biosurfactant

The microstructure of the aqueous solutions of purified acidic Sophorolipid (SL) has previously been studied using highly sophisticated methods such as SANS and Cryo-TEM. We were interested in whether (a) the main findings also apply to commercially available SL (which is a mixture of acidic and lactonic SL) and (b) more readily available methods such as DLS can be used to gain insight into the molecular aggregation of SL. Our work was motivated by the increasing interest in biosurfactants for applications in personal and household care. Moreover, the origin behind the more or less lack of rheological response to changes in pH is of practical relevance, as it is somewhat unusual for a carboxylate-group containing surfactant. By using DLS microrheology, we could elucidate the aggregation structure and dynamics of the surfactant on a microscopic scale. Surprisingly, the different degrees of protonation only impacted the microscopic properties such as exchange kinetics and the plateau values of the storage moduli.

Effect of Water and Salt on the Colloidal Stability of Latex Particles in Ionic Liquid Solutions

The colloidal stability of sulfate (SL) and polyimidazolium-modified sulfate (SL-IP-2) latex particles was studied in an ionic liquid (IL) of ethylammonium nitrate (EAN) and its water mixtures. Aggregation rates were found to vary systematically as a function of the IL-to-water ratio. Repulsive electrostatic interactions between particles dominated at low IL concentrations, while they were significantly screened at intermediate IL concentrations, leading to destabilization of the dispersions. When the IL concentration was further increased, the aggregation of latex particles slowed down due to the increased viscosity and finally, a striking stabilization was observed in the IL-rich regime close to the pure IL solvent. The latter stabilization is due to the formation of IL layers at the interface between particles and IL, which induce repulsive oscillatory forces. The presence of the added salt in the system affected differently the structure of the interfaces around SL and SL-IP-2 particles. The sign of the charge and the composition of the particle surfaces were found to be the most important parameters affecting the colloidal stability. The nature of the counterions also plays an important role in the interfacial properties due to their influence on the structure of the IL surface layers. No evidence was observed for the presence of long-range electrostatic interactions between the particles in pure ILs. The results indicate that the presence of even low concentrations of water and salt in the system (as undesirable impurities) can strongly alter the interfacial structure and thus, the aggregation mechanism in particle IL dispersions.

Stable and Efficient Photoinduced Charge Transfer of MnFe2O4/Polyaniline Photoelectrode in Highly Acidic Solution

Tailoring conductive polymers with inorganic photocatalysts, which provide photoinduced electron-hole generation, have significantly enhanced composites leading to excellent photoelectrodes. In this work, MnFe2O4 nanoparticles prepared by a hydrothermal method were combined with polyaniline to prepare mixed (hybrid) slurries, which were cast onto flexible FTO to prepare photoelectrodes. The resulting photoelectrodes were characterized by XRD, FESEM, HRTEM and UV-VIS. The photoelectrochemical performance was investigated by linear sweep voltammetry and chronoamperometry. The photocurrent achieved by MnFe2O4/Polyaniline was 400 μA/cm2 at 0.8 V vs. Ag/AgCl in Na2SO4 (pH = 2) at 100 mW/cm2, while polyaniline alone achieved only 25 μA/cm2 under the same conditions. The best MnFe2O4/Polyaniline displayed an incident photon-to-current conversion efficiency (IPCE) and applied bias photon-to-current efficiency (ABPE) of 60% at 405 nm wavelength, and 0.17% at 0.8 V vs. Ag/AgCl, respectively. High and stable photoelectrochemical performance was achieved for more than 900 s in an acidic environment.

Prediction of Aqueous Solution Surface Tension of Some Surfactant Mixtures and Composition of Their Monolayers at the Solution–Air Interface

Measurements of the surface tension of the aqueous solution of SDDS mixture with fluorocarbon surfactants (FC) were carried out and considered in light of the surface tension of aqueous solutions of individual surfactants. Similar analyses were made for many other aqueous solutions of binary and ternary mixtures, taking into account the literature data of the surface tension of aqueous solutions of TX100, TX114, TX165, SDDS, SDS, CTAB, CPyB and FC. The possibility of predicting the surface tension of the aqueous solution of many surfactant mixtures from that of the mixture components using both the Szyszkowski, Fainerman and Miller and Joos concepts was analyzed. The surface tension of the aqueous solutions of surfactant mixtures was also considered based on the particular mixture component contribution to the water surface tension reduction. As a result, the composition of the mixed surface layer at the solution–air interface was discussed and compared to that which was determined using the Hua and Rosen concept. As follows from considerations, the surface tension of the aqueous solution of binary and ternary surfactant mixtures can be described and/or predicted.

Equilibrium, Kinetic, and Thermodynamic Studies of Cationic Dyes Adsorption on Corn Stalks Modified by Citric Acid

The modification of agricultural wastes and their use as low-cost and efficient adsorbents is a prospective pathway that helps diminish waste and decrease environmental problems. In the present research, the natural adsorption capacity of corn stalks (CS) was improved by modification of their surface with citric acid. The adsorption capacity of the modified corn stalks (CS-C) was determined with the help of cationic dyes (methylene blue and malachite green). The equilibrium, kinetics, and thermodynamics of the cationic dyes on CS-C were studied. The Langmuir isotherm model best fitted the data both for methylene blue and malachite green adsorption on CS-C. The adsorption kinetics of the cationic dyes was well described by the pseudo-second order model. Thermodynamic studies revealed that adsorption of the cationic dyes on CS-C was an endothermic process. Negative results of ΔGo (between −31.8 and −26.3 kJ mol−1) indicated that the adsorption process was spontaneous in all the tested temperatures. The present study verified that citric acid-modified corn stalks can be used as a low-cost and effective adsorbent for removal of cationic dyes from aqueous solutions.

Dense Phases of γ-Gliadins in Confined Geometries

The binary phase diagram of γ-gliadin, a wheat storage protein, in water was explored thanks to the microevaporator, an original PDMS microfluidic device. This protein, usually qualified as insoluble in aqueous environments, displayed a partial solubility in water. Two liquid phases, a very dilute and a dense phase, were identified after a few hours of accumulation time in the microevaporator. This liquid–liquid phase separation (LLPS) was further characterized through in situ micro-Raman spectroscopy of the dilute and dense protein phases. Micro-Raman spectroscopy showed a specific orientation of phenylalanine residues perpendicular to the PDMS surfaces only for the diluted phase. This orientation was ascribed to the protein adsorption at interfaces, which would act as nuclei for the growth of dense phase in bulk. This study, thanks to the use of both aqueous solvent and a microevaporator, would provide some evidence for a possible physicochemical origin of the gliadin assembly in the endoplasmic reticulum of albumen cells, leading to the formation of dense phases called protein bodies. The microfluidic tool could be used also in food science to probe protein–protein interactions in order to build up phase diagrams.

Performance of Oleic Acid and Soybean Oil in the Preparation of Oil-in-Water Microemulsions for Encapsulating a Highly Hydrophobic Molecule

This work analyzes the dispersion of a highly hydrophobic molecule, (9Z)-N-(1,3-dihydroxyoctadecan-2-yl)octadec-9-enamide (ceramide-like molecule), with cosmetic and pharmaceutical interest, by exploiting oil-in-water microemulsions. Two different oils, oleic acid and soybean oil, were tested as an oil phase while mixtures of laureth-5-carboxylic acid (Akypo) and 2-propanol were used for the stabilization of the dispersions. This allowed us to obtain stable aqueous-based formulations with a relatively reduced content of oily phase (around 3% w/w), that may enhance the bioavailability of this molecule by its solubilization in nanometric oil droplets (with a size range of 30–80 nm), that allow the incorporation of a ceramide-like molecule of up to 3% w/w, to remain stable for more than a year. The nanometric size of the droplet containing the active ingredient and the stability of the formulations provide the basis for evaluating the efficiency of microemulsions in preparing formulations to enhance the distribution and availability of ceramide-like molecules, helping to reach targets in cosmetic and pharmaceutical formulations.

Bacteria Cell Hydrophobicity and Interfacial Properties Relationships: A New MEOR Approach

For microbial enhanced oil recovery (MEOR), different mechanisms have been introduced. In some of these papers, the phenomena and mechanisms related to biosurfactants produced by certain microorganisms were discussed, while others studied the direct impacts of the properties of microorganisms on the related mechanisms. However, there are only very few papers dealing with the direct impacts of microorganisms on interfacial properties. In the present work, the interfacial properties of three bacteria MJ02 (Bacillus Subtilis type), MJ03 (Pseudomonas Aeruginosa type), and RAG1 (Acinetobacter Calcoaceticus type) with the hydrophobicity factors 2, 34, and 79% were studied, along with their direct impact on the water/heptane interfacial tension (IFT), dilational interfacial visco-elasticity, and emulsion stability. A relationship between the adsorption dynamics and IFT reduction with the hydrophobicity of the bacteria cells is found. The cells with highest hydrophobicity (79%) exhibit a very fast dynamic of adsorption and lead to relatively large interfacial elasticity values at short adsorption time. The maximum elasticity values (at the studied frequencies) are observed for bacteria cells with the intermediate hydrophobicity factor (34%); however, at longer adsorption times. The emulsification studies show that among the three bacteria, just RAG1 provides a good capability to stabilize crude oil in brine emulsions, which correlates with the observed fast dynamics of adsorption and high elasticity values at short times. The salinity of the aqueous phase is also discussed as an important factor for the emulsion formation and stabilization.