Influence of the Mixtures of Vegetable Oil and Vitamin E over the Microstructure and Rheology of Organogels

Candelilla wax (CW) and 12-hydroxystearic acid (12HSA) are classic solid-fiber-matrix organogelators. Despite the high number of studies using those ingredients in oily systems, there is scarce literature using a mixture of oil and antioxidants. Vitamin E (VE) is an important candidate for its lipophilicity and several applications on pharmaceutical, cosmetics, and food industries. In this work, we investigated the influences of mixtures between vegetable oil (VO) and VE on the microstructures and rheological properties of CW and 12HSA organogels. A weak gel (G′′/G′ > 0.1) with a shear-thinning behavior was observed for all samples. The presence of VE impacted the gel strength and the phase transition temperatures in a dose-dependent pattern. Larger and denser packed crystals were seen for 12HSA samples, while smaller and more dispersed structures were obtained for CW organogels. The results obtained in this work allowed the correlation of the structural and mechanical properties of the organogels, which plays an important role in the physical-chemical characteristics of these materials.

Влияние дейтерирования на фазовые переходы в (NH-=SUB=-4-=/SUB=-)-=SUB=-3-=/SUB=-VOF-=SUB=-5-=/SUB=-

The (ND4)3VOF5 crystal was grown with a high degree of deuteration (D ~ 92%). Structural and thermophysical studies have been carried out, the parameters of phase transitions have been determined. It was found that the deuteration of the ammonium cation in (NH4)3VOF5 led to a change in the chemical pressure, which was accompanied by an increase in the unit cell volume and an increase in the phase transition temperatures. The baric coefficients dTi / dp were determined and the phase T-p diagram (ND4)3VOF5 was constructed. A decrease in the temperature stability of the initial cubic phase Fm 3m in (ND4)3VOF5, as well as a wedging out of the intermediate monoclinic phase at a lower pressure as compared to (NH4)3VOF5, was found.

Novel Naproxen Salts with Increased Skin Permeability

The paper presents the synthesis, full identification, and characterization of new salts-L-proline alkyl ester naproxenates [ProOR][NAP], where R was a chain from ethyl to butyl (including isopropyl). All obtained compounds were characterized by Nuclear Magnetic Resonance (NMR), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffractometry (XRD), and in vitro dissolution studies. The specific rotation, phase transition temperatures (melting point), and thermal stability were also determined. In addition, their lipophilicity, permeability, and accumulation in pigskin were determined. Finally, toxicity against mouse L929 fibroblast cells was tested. The obtained naproxen derivatives showed improved solubility and higher absorption of drug molecules by biological membranes. Their lipophilicity was lower and increased with the increase in the alkyl chain of the ester. The derivative with isopropyl ester had the best permeability through pigskin. The use of L-proline isopropyl ester naproxenate increased the permeation of naproxen through the skin almost four-fold. It was also shown that the increase in permeability is not associated with additional risk: all compounds had a similar effect on cell viability as the parent naproxen.

Phase transitions in natural C-O-H-N-S fluid inclusions - implications for gas mixtures and the behavior of solid H2S at low temperatures

C–O–H–N–S-bearing fluids are known as one of the most challenging geochemical systems due to scarcity of available experimental data. H2S-rich fluid systems were recognized in a wide array of world-class mineral deposits and hydrocarbon reservoirs. Here we report on a nature of low-temperature (T ≥ −192 °C) phase transitions observed in natural CH4–H2S–CO2–N2–H2O fluid inclusions, which are modeled as closed thermodynamic systems and thus serve as natural micro-laboratories representative of the C–O–H–N–S system. For the first time, we document solid–solid H2S (α ↔ β ↔ γ) transitions, complex clathrates and structural transformations of solid state H2S in natural inclusion gas mixtures. The new data on Raman spectroscopic features and a complete sequence of phase transition temperatures in the gas mixtures contribute to scientific advancements in fluid geochemistry. Enhanced understanding of the phase equilibria in the C–O–H–N–S system is a prerequisite for conscientious estimation of P-T-V-X properties, necessary to model the geologic evolution of hydrocarbon and mineral systems. Our findings are a driver for the future research expeditions to extraterrestrial H2S-rich planetary systems owing to their low temperature environments.

PHASE TRANSITION STUDIES OF CHOLESTERYL PALMITATE, CHOLESTERYL DECANOATE AND THEIR MIXTURES USING DIELECTRIC, EPR AND DTA TECHNIQUES

The phase transition of two liquid crystalline materials, namely cholesteryl palmitate and cholesteryl decanoate and their mixtures (by weight)are studied using dielectric, Electron paramagnetic resonance (EPR) and differential thermal analysis (DTA) techniques. From the dielectric measurements, the phase transition temperatures were determined from the discontinuities in the curve between dielectric constant and temperatures for all the samples investigated. Further, since mixing of two liquid crystals modifies the transition of phases, the measurements were carried out on the mixtures of the two liquid crystals. Order parameter for each sample was calculated at varying temperatures by measuring the hyperfine splitting of three line EPR spectrums. The discontinuities in the curve between order parameter and the temperature again indicated the phase transition of the liquid crystals and their mixtures. A DTA study on these samples was also carried out in order to probe further their transitional behaviour. The DTA records of both the liquid crystals and their mixtures support the transition behaviour observed from the dielectric and EPR measurements.

Thermal and Mesomorphic Investigations of 1:1 Supramolecular Assemblies of 4-[(4-(n-Alkoxy)phenylimino)methyl]benzoic Acids Having Symmetrical and Un-Symmetrical Terminal Chain Lengths

Thermal and mesomorphic properties of possible 1:1 supramolecular complexes (SMCs) (Im/In) designed from two members of 4-[(4-(n-alkoxy)phenylimino)methyl]benzoic acid with symmetrical or un-symmetrical alkoxy terminal flexible chains (carbons of m and n = 6, 8 and 16), were analyzed by differential scan-calorimetry (DSC), thermogravemetric (TG) analysis, and their mesophases identified by polarized optical microscopy (POM). The equimolecular mixtures of the two acids possess symmetrical and un-symmetrical terminal lengths. The mesomorphic properties of the binary mixtures were examined as a function of the total alkoxy chain length on both sides. Results revealed that the nematic mesophase temperature range increases as the total terminal length increases for all designed un-symmetrical mixtures. A comparison was constructed between the formed SMCs and of those of the previously prepared 4-n-alkoxyphenylazo benzoic acids as well as the 4-n-alkoxy benzoic acids, to examine the impact of mesogenic core on the mesomorphic properties. The comparison indicated that as the mesogenic portion lengthens the thermal mesophase stability exhibits higher values of phase transition temperatures; whereas, the azo and Schiff base moieties exhibited near thermal properties.

Conducting and dielectric properties of Na3Fe2(PO4)3 and Na2FePO4F

In this research, the structure parameters, conducting and dielectric properties of Na3Fe2(PO4)3 and Na2FePO4F polycrystals were studied obtained by solid-phase synthesis. The phase transition temperatures, conducting and dielectric parameters of Na3Fe2(PO4)3 and Na2FePO4F polycrystals were refined. A comparative evaluation of the conductive properties of Na3Fe2(PO4)3 and Na2FePO4F polycrystals is given in this article. The prospects of using of Na3Fe2(PO4)3 and Na2FePO4F are justified as electrode materials in sodium ion batteries.

Magnetic and Magnetostrictive Properties of Ni50Mn20Ga27Cu3 Rapidly Quenched Ribbons

The influence of the rapid solidification technique and heat treatment on the martensitic transformation, magnetic properties, thermo- and magnetic induced strain and electrical resistivity is investigated for the Cu doped NiMnGa Heusler-based ferromagnetic shape memory ribbons. The martensitic transformation temperatures are unexpectedly low (below 90 K—which can be attributed to the disordered texture as well as to the uncertainty in the elements substituted by the Cu), preceded by a premartensitic transformation (starting at around 190 K). A thermal treatment slightly increases the transformation as well as the Curie temperatures. Additionally, the thermal treatment promotes a higher magnetization value of the austenite phase and a lower one in the martensite. The shift of the martensitic transformation temperatures induced by the applied magnetic field, quantified from thermo-magnetic and thermo-magnetic induced strain measurements, is measured to have a positive value of about 1 K/T, and is then used to calculate the transformation entropy of the ribbons. The magnetostriction measurements suggest a rotational mechanism in low fields for the thermal treated samples and a saturation tendency at higher magnetic fields, except for the temperatures close to the phase transition temperatures (saturation is not reached at 5 T), where a linear volume magnetostriction cannot be ruled out. Resistivity and magnetoresistance properties have also been measured for all the samples.