Phase diagram of the Li2SO4–Na2SO4 system

The thermal analysis and X-ray powder diffraction studies of the Li₂SO₄–Na₂SO₄ system, including the high-temperature X-ray diffraction technique, have elucidated four phases of variable composition: three solid solutions based on the α-Li₂SO₄, α-Na₂SO₄, and α-LiNaSO₄ high-temperature polymorphs, and a low-temperature β-LiNaSO₄ phase. α-Na₂SO₄-Base solid solution disintegrates into two phases via a monotectoid phase transformation. It is quite probable that the monotectoid process is related to the conversion of the second-order phase transition to the first-order phase transition.     

Surface modification of poly(tetrafluoroethylene) and poly(ethylene terephthalate) films via environmental crazing

This work addresses the phenomenon of the development of a patterned surface relief on polymer films via different modes of environmental crazing. Commercial films of semicrystalline poly(tetrafluoroethylene) (PTFE) and amorphous glassy poly(ethylene terephthalate) (PET) were subjected to tensile drawing in the presence of physically active liquid environments (carbon tetrachloride or aliphatic alcohols). The structure parameters and wettability of the modified films were studied by AFM, SEM, profilometer measurements and contact angle measurements. Environmental intercrystallite crazing of PTFE is accompanied by the development of an unstable structure with a high free surface, which experiences marked strain recovery upon unloading. As a result of the relief formation, PTFE hydrophobicity is enhanced (the water contact angle increases by 25°). Classical environmental crazing of PET films is accompanied by the formation of an anisotropic surface relief which is an assembly of crazes oriented perpendicular to the direction of tensile drawing, thus leading to the phenomenon of anisotropic wetting. The proposed approach for structural surface modification makes it possible to use the advantages of surface instability and spontaneous self‐organization of the polymer towards the development of a unique surface microrelief. © 2020 Society of Chemical Industry     

Effect of Acidic Peptization on Formation of Highly Photoactive TiO2 Films Prepared without Heat Treatment

Nowadays, it is a great challenge to synthesize crystalline TiO₂ nanostructures using low‐temperature methods without annealing stage. Such an approach allows to perform functional and structural modification in the formed crystalline phase by thermally unstable compounds, such as biomaterials, MOFs, dye sets in situ, which was previously considered impossible. In this work, we have developed and analyzed the effect of acidic peptization on formation of highly photoactive titania crystallites in an aqueous solution using titanium tetraisopropylate as a precursor. Acids with different dissociation degrees in water were used as peptizing mediators to determine the effect of protonation on sol formation. The dip‐coating films were obtained with consequent drying of the sols via evaporation of the solvent. The as‐prepared catalysts were characterized by X‐ray diffraction, AFM microscopy, UV–V is spectroscopy, Brunauer–Emmett–Teller surface area. The aggregate size of TiO₂ in the colloidal suspension solution was measured by dynamic light scattering. Photocatalytic activity of films was studied by decomposition of Rhodamine B dye. It is found that the size of colloids in an aqueous solution is proportional to the protonation degree of the surface of particles and does not depend on the [Ti⁴⁺]/[H⁺] ratio, and peptization under weakly acidic conditions leads to anisotropic rod‐like nanoparticles. The highest photocatalytic activity was exhibited by the TiO₂–HCl‐based coatings, ~3.5 times higher than that of the Acet.‐prepared sample.     

Mechanochemical preparation of kaempferol intermolecular complexes for enhancing the solubility and bioavailability

Abstract

In this study, complexes of kaempferol (KF) with polysaccharide arabinogalactan (AG) and disodium glycyrrhizinate (Na₂GA) were prepared through mechanochemical technique to improve the solubility and bioavailability of KF. The physicochemical properties and the interactions of KF with AG/Na₂GA were investigated through dissolution, SEM, XRD, and DSC studies. The reduction of particle sizes and destruction of crystal forms revealed the formation of solid dispersion which may have assisted the dissolution of the drug. The accelerated stability study showed higher stability for KF–Na₂GA complex. In vivo pharmacokinetic study was performed to observe the plasma drug concentrations for KF complexes. Mechanochemical complexation of KF with AG/Na₂GA improved the pharmacological activity as evident by the inhibitory potential of the complexes towards carbohydrate metabolic enzymes. In vivo studies were performed in STZ-induced diabetic mice, where the group treated with KF–AG complex showed better liver and kidney function and lower blood glucose levels than pure KF. Therefore, mechanochemical complexes of KF with polysaccharide or glycyrrhizate may serve as a promising formulation for the treatment of diabetes.     

Oxidation of ZrB2–SiC–ZrSi2 ceramics in oxygen

The oxidation of ZrB₂–SiC and ZrB₂–SiC–ZrSi₂ ceramics of different composition has been studied experimentally at 1500 °C in pure oxygen for up to 50 h. ZrB₂–SiC–ZrSi₂ ceramics proved to be the most oxidation-resistant at ZrSi₂ contents of less then 4 wt%. These ceramics were more oxidation-resistant than ZrB₂–SiC ceramics. An analytical model of growth kinetics for a multilayered scale based on an oxidation–diffusion balance was developed and tested.     

Behaviour of an optically trapped probe approaching a dielectric interface

Abstract

The way in which reflection of the trapping beam from a dielectric interface influences the distance of the trapped sphere from the beam waist is studied theoretically and experimentally. The reflected wave interferes with the incident wave and they create a standing-wave component in the total axial intensity distribution. This component then modulates the trapping potential and creates several possible equilibrium positions for the trapped sphere. When the beam waist approaches the surface, the potential profile changes, which consequently causes jumps of the trapped probe from its current location to a deeper potential well. We suggested theoretically and proved experimentally that the magnitude of these unwanted jumps between the neighbouring equilibrium positions can be decreased by a suitable size of the sphere.     

Self-diffusion of low-generation PAMAM dendrimers with hydroxyl surface groups in solutions: a general regularity

An experimental study of the self-diffusion and nuclear magnetic relaxation of poly(amidoamine) dendrimers with hydroxyl surface groups (PAMAM-OH) dissolved in methanol over a wide range of concentration (?) is reported. It is shown that experimental concentration dependences of PAMAM-OH self-diffusion coefficients (D) can be reduced to the so-called generalized ? dependence. Over macromolecular concentration range studied, the generalized concentration dependence of PAMAM-OH D coincides with analogous curve obtained for poly(allylcarbosilane) dendrimers of high generations. This result confirms the existence of common regularities of the dendritic macromolecule self-diffusion, and their independence of the individual physicochemical and structural properties of dendrimer, solvent, and features of their interactions in the given systems. The concentration dependence of the PAMAM-OH diffusion also exhibits a clear signature of an inflexible molecule.