Application of Porous Glasses in Ophthalmic Prosthetic Repair

The ophthalmic prosthetic materials besides their necessary cosmetic view should be biologically inert. Silica porous glasses can be fabricated to satisfy the cosmetic requirements while their pores can be filled with medicines that would help to avoid complications when contacting the biological tissues. In this work the ability of different silica porous glasses to support a necessary level of the medicine around itself for long periods of time was studied. Hentamicini sulphate antibiotic was used as the biologically active substance while vitamin B₆ was employed as the nutrient. The concentration of the above substances in the normal saline solution that simulated the lachrymal liquid was controlled by the luminescent technique. It was demonstrated that the silica porous glass that was obtained by phase separation at 490°C without subsequent removal of the residual silica gel supported the necessary level of medicines around itself for the longest period of time.     

Use of photodegradable inhibitors in UV-curable compositions to form polymeric 2D-structures by visible light

The process of two-wave photopolymerization of a UV-curable composition with an optically degrading inhibitor is considered. By numerical simulation, it is shown that in the composition layer uniformly exposed to UV-radiation, such systems allow getting segments with different conversion under the action of inhomogeneous visible light. Based on the data on the photopolymerization kinetics of the compositions from triethylene glycol dimethacrylate (TEGDMA) and bisphenol-A glycidyl dimethacrylate (bis-GMA) with the UV-initiator 2,2-dimethoxy-2-phenylacetophenone (DMPA), it was shown that 3,5-di-tert-butyl-o-benzoquinone (35Q) with N,N-dimethylaniline (DMA, “Aldrich”, 99%) can serve as an inhibitor that degrades under action of visible radiation. Combining inhomogeneous visible light generated with a conventional DLP-projector and uniform UV-radiation of LED (365 nm) the two-wave lithographic process was implemented to create polymeric 2D-structures in 20 μm layer of the compositions from TEGDMA (70)/bis-GMA (30)/DMPA (0.05 wt%)/35Q (0.5 wt%)/DMA (1 wt%).     

Molar enthalpy of vaporization of ethanol-gasoline mixtures and their colloid state

Vapour pressure measurements are used to evaluate the enthalpy of vaporization of ethanol-gasoline mixtures. Partial molar values are also derived. The dispersed structure of ethanol-gasoline fuel is studied for the first time using the method of correlation spectroscopy of scattered light. A large range of dispersed particle sizes in different alcohol-gasoline systems is found. The dependence of the mean radius of drops on ethanol content is determined. It is found that coalescence phenomenon occurs in the systems when extra ethanol is added.     

Direct Measurement of Fusion Enthalpy of LaAlO3 and Comparison of Energetics of Melt,Glass, and Amorphous Thin Films

Enthalpy of fusion and melting temperature of perovskite LaAlO₃ were measured using thermal analysis method as 124 ± 10 kJ/mol at 2134 ± 10°C, providing a value of 52 ± 4 J·(mol·K)^?1 for entropy of fusion. Crystallization enthalpy of amorphous LaAlO₃ thin films was found to change from ?24 to ?17 kJ/mol with decrease in film thickness from 100 to 20 nm. Differences in energetics of amorphous LaAlO₃ films and glass cannot be explained exclusively by surface energy contribution but must reflect differences in structure between films and glasses in this system.     

Revisiting tetranitrophenolsulfonephthalein

Among the vast series of phenolsulfonephthalein dyes, the nitro derivatives and especially 3,3′,5,5′‐tetranitrophenolsulfonephthalein (nitrophenol crimson) remain practically unexplored, whereas the halogen and alkyl derivatives have been studied comprehensively. This striking difference is probably due to the enormous influence of the four NO₂ groups on the properties of the dye. As a result, the protolytic behaviour is unlike even that of tetrabromo phenolsulfonephthalein, and the recognised scheme of acid–base and tautomeric equilibrium of the sulfonephthaleins is unable to explain it. The molecular form H₂R was isolated as a sultonic tautomer, and an X‐ray crystal structure analysis was carried out. Our studies of the UV‐vis absorption spectra in water, methanol, dimethyl sulfoxide, acetonitrile, acetone, and dichloromethane, as well as in aqueous micellar solutions of surfactants, allowed us to evaluate the true molar absorptivity of the dianion R^2?, and to elucidate the enormous tendency to form yellow trianionic carbinol ROH^3?, even in the presence of traces of H₂O. Nuclear magnetic resonance and electrospray data confirm the proposed scheme of ionisation and tautomerism of nitrophenol crimson.     

Structure and Thermal Expansion of YSZ and La2Zr2O7 Above 1500°C from Neutron Diffraction on Levitated Samples

High‐temperature time‐of‐flight neutron diffraction experiments were performed on cubic yttria‐stabilized zirconia (YSZ, 10 mol% YO_1.5) and lanthanum zirconate (LZ) prepared by laser melting. Three spheroids of each composition were aerodynamically levitated and rotated in argon flow and heated with a CO₂ laser. Unit cell, positional and atomic displacement parameters were obtained by Rietveld analysis. Below ~1650°C the mean thermal expansion coefficient (TEC) for YSZ is higher than for LZ (13 ± 1 vs. 10.3 ± 0.6) × 10^?6/K. From ~1650°C to the onset of melting of LZ at ~2250°C, TEC for YSZ and LZ are similar and within (7 ± 2) × 10^?6/K. LZ retains the pyrochlore structure up to the melting temperature with Zr coordination becoming closer to perfectly octahedral. Congruently melting LZ is La deficient. The occurrence of thermal disordering of oxygen sublattice (Bredig transition) in defect fluorite structure was deduced from the rise in YSZ TEC to ~25 × 10^?6/K at 2350°C–2550°C with oxygen displacement parameters (U_iso) reaching 0.1 Å², similar to behavior observed in UO₂. Acquisition of powder‐like high‐temperature neutron diffraction data from solid‐levitated samples is feasible and possible improvements are outlined. This methodology should be applicable to a wide range of materials for high‐temperature applications.     

Developmental and Reproductive Effects of Iron Oxide Nanoparticles in Arabidopsis thaliana

Increasing use of iron oxide nanoparticles in medicine and environmental remediation has led to concerns regarding exposure of these nanoparticles to the public. However, limited studies are available to evaluate their effects on the environment, in particular on plants and food crops. Here, we investigated the effects of positive (PC) and negative (NC) charged iron oxide (Fe₂O₃) nanoparticles (IONPs) on the physiology and reproductive capacity of Arabidopsis thaliana at concentrations of 3 and 25 mg/L. The 3 mg/L treated plants did not show evident effects on seeding and root length. However, the 25 mg/L treatment resulted in reduced seedling (positive-20% and negative-3.6%) and root (positive-48% and negative-negligible) length. Interestingly, treatment with polyethylenimine (PEI; IONP-PC coating) also resulted in reduced root length (39%) but no change was observed with polyacrylic acid (PAA; IONP-NC coating) treatment alone. However, treatment with IONPs at 3 mg/L did lead to an almost 5% increase in aborted pollen, a 2%–6% reduction in pollen viability and up to an 11% reduction in seed yield depending on the number of treatments. Interestingly, the treated plants did not show any observable phenotypic changes in overall size or general plant structure, indicating that environmental nanoparticle contamination could go dangerously unnoticed.     

Microwave Dielectrics in the (La1/2Na1/2)TiO3–Ca(Fe1/2Nb1/2)O3 System

Dielectric properties of the system (1 − x)(La_1/2Na_1/2)TiO₃– _x Ca(Fe_1/2Nb_1/2)O₃, where 0.4 # x # 0.6, have been investigated at microwave frequencies. The temperature coefficient of resonant frequency (τ_f), nearly 0 ppm/°C, was realized at x = 0.58. These ceramics had perovskite structure and showed relatively low dielectric losses. A new dielectric material applicable to microwave devices having Q · f of 12000–14000 GHz and a dielectric constant (ε_r) of 59–60 has been obtained at 1300–1350°C for 5–15 h sintering.     

Exfoliated production of single- and multi-layer graphenes and carbon nanofibres from the carbonisation of a co-polymer

Non-catalysed growth methodologies of carbon nanomaterial synthesis can represent lower costs and greener approaches and cause less damage to the nanomaterial. During the carbonisation of a polyacrylonitrile-based co-polymer, carbon nanofibres (CNFs) and single- and multi-layer graphenes (SLG and MLG) are generated. The accumulated fragmentation products of the co-polymer coalesce to form CNFs that radiate away from the monolith, whose dimensions are linked to their template growth along crests, which were formed from the out-gassing of volatile products of the polymer during the stabilisation step. The slight shrinkage of the carbonising monolith also leads to exfoliation of larger areas of the surface yielding single- and multi-layered graphenes. These results reveal a potentially useful process for the facile production of carbon nanomaterials.     

Selective adsorption of multivalent ions into TiC-derived nanoporous carbon

A TiC-derived carbon (TiC-CDC) was prepared, and the adsorption of large hexacyanocobaltate and tetrabutylammonium ions of approximately same size was examined on this carbon. While selectively absorbing these large ions, it rejects smaller chloride and ammonium ions in mixed electrolyte solutions. The result demonstrates the important role of electrostatic repulsive forces, space-efficient charge packing and hydrophobic ion interactions with the pore walls of TiC-CDC, similar to what is known for a variety of biological membranes.