The impact of different volume fractions of crystalline structures on the electrochemical behaviour of Mg67Zn29Ca4 alloys for biomedical applications

ABSTRACT

In this work, the influence of various volume fractions of the crystalline phase in an amorphous matrix of Mg₆₇Zn₂₉Ca₄ alloys was investigated for its corrosion resistance for biodegradable applications. An amorphous Mg₆₇Zn₂₉Ca₄ alloy was successfully fabricated using melt casting into a copper mould. Then, to obtain different ratios of the crystalline phase in an amorphous matrix, the obtained amorphous rods with 3?mm diameters were annealed at 190, 230, 250, and 400°C. The volume fraction of the crystalline phase was measured by X-ray diffraction, and the microstructures of the obtained alloys were determined based on scanning electron microscopy images. Electrochemical testing was conducted in simulated body fluid at 37°C. This report shows that the ratio of the volume fractions of amorphous and crystalline phases in alloy microstructures strongly influences their corrosion behaviours. The alloy with a fully amorphous structure was the most resistive in the analysed media.     

Experimental Results on the Fixed Matrix Regenerator Effectiveness for a Glass Stove Furnace

This paper presents experimental results on the effectiveness of regenerators working integrally with an open hearth glass furnace. The presented data refer to two apparatus of identical size and geometry arranged in parallel but operating in a one-period-shifted mode. The effectiveness figures with corresponding uncertainties for each unit have been determined by making use of experimental data accounting for both heating and cooling periods. For the heating period the effectiveness is bound within the range 0.8795 ± 0.0683 to 0.9272 ± 0.0715. Considering those for the cooling period the effectiveness holds 0.9142 ± 0.0305 to 0.9499 ± 0.0329, shown to be accompanied by a bit lower uncertainty. Due to the difference in effectiveness, averaging was applied to calculate mean effectiveness value measured as weighted based on the uncertainties for both periods. As the result, the final averaged effectiveness of the investigated regenerators was found to be within the ranges of 0.9153 ± 0.0278 to 0.9367 ± 0.0296.     

Solvent effects on the rates and mechanisms of reaction of phenols with free radicals

The rates of formal abstraction of phenolic hydrogen atoms by free radicals, Y* + ArOH --> YH + ArO*, are profoundly influenced by the hydrogen-bond-accepting and anion-solvation abilities of solvents, by the electron affinities and reactivities (Y-H bond dissociation enthalpies) of radicals, and by the phenol's ring substituents. These apparently simple reactions can occur by at least three different, nonexclusive mechanisms: hydrogen atom transfer, proton-coupled electron transfer, and sequential proton-loss electron transfer. The delicate balance among these mechanisms depends on both the environment and the reactants. The main features of these mechanisms are described, together with some interesting kinetic consequences.     

Integrated three-dimensional shape and reflection properties measurement system

Creating accurate three-dimensional (3D) digitalized models of cultural heritage objects requires that information about surface geometry be integrated with measurements of other material properties like color and reflectance. Up until now, these measurements have been performed in laboratories using manually integrated (subjective) data analyses. We describe an out-of-laboratory bidirectional reflectance distribution function (BRDF) and 3D shape measurement system that implements shape and BRDF measurement in a single setup with BRDF uncertainty evaluation. The setup aligns spatial data with the angular reflectance distribution, yielding a better estimation of the surface's reflective properties by integrating these two modality measurements into one setup using a single detector. This approach provides a better picture of an object's intrinsic material features, which in turn produces a higher-quality digitalized model reconstruction. Furthermore, this system simplifies the data processing by combining structured light projection and photometric stereo. The results of our method of data analysis describe the diffusive and specular attributes corresponding to every measured geometric point and can be used to render intricate 3D models in an arbitrarily illuminated scene.     

Poly(methyl vinyl ether‐alt‐maleic anhydride) functionalized with 3‐aminophenylboronic acid: A new boronic acid polymer for sensing diols in neutral water

Amidation of poly(methyl vinyl ether‐alt‐maleic anhydride) with 3‐aminophenylboronic acid was used to prepare a new boronic acid polymer. The binding of catechol dye, Alizarin Red S to the polymer obtained resulted in getting a stable, colored sensor which was used to establish association constants with different diols in competitive assay. The binding of different diols was readily detected by color change and absorbance values measured at 450 nm were used to calculate the association constants. The polymer obtained formed high‐affinity complexes with ribonucleosides, particularly cytidine and uridine. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40778.     

The Composites of PCL and Tetranuclear Titanium(IV)-oxo Complexes as Materials Exhibiting the Photocatalytic and the Antimicrobial Activity

Excessive misuse of antibiotics and antimicrobials has led to a spread of microorganisms resistant to most currently used agents. The resulting global threats has driven the search for new materials with optimal antimicrobial activity and their application in various areas of our lives. In our research, we focused on the formation of composite materials produced by the dispersion of titanium(IV)-oxo complexes (TOCs) in poly(ε-caprolactone) (PCL) matrix, which exhibit optimal antimicrobial activity. TOCs, of the general formula [Ti₄O₂(OⁱBu)₁₀(O₂CR’)₂] (R’ = PhNH₂ (1), C₁₃H₉ (2)) were synthesized as a result of the direct reaction of titanium(IV) isobutoxide and 4-aminobenzoic acid or 9-fluorenecarboxylic acid. The microcrystalline powders of (1) and (2), whose structures were confirmed by infrared (IR) and Raman spectroscopy, were dispersed in PCL matrixes. In this way, the composites PCL + nTOCs (n = 5 and 20 wt.%) were produced. The structure and physicochemical properties were determined on the basis of Raman microscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), electron paramagnetic resonance spectroscopy (EPR), and UV–Vis diffuse reflectance spectroscopy (DRS). The degree of TOCs distribution in the polymer matrix was monitored by scanning electron microscopy (SEM). The addition of TOCs micro grains into the PCL matrix only slightly changed the thermal and mechanical properties of the composite compared to the pure PCL. Among the investigated PCL + TOCs systems, promising antibacterial properties were confirmed for samples of PCL + n(2) (n = 5, 20 wt.%) composites, which simultaneously revealed the best photocatalytic activity in the visible range.     

Effect of randomly methylated beta-cyclodextrin on physical properties of soils

The application of cyclodextrins in several soil remediation technologies has been increasingly studied, but little is known about their effects on soil physical properties. One of the popular soil remediation additives, randomly methylated beta-cyclodextrin (RAMEB), was found to significantly alter surface and pore properties of soil clay minerals. Therefore, in this paper we studied the effect of various RAMEB doses on physical properties of selected soils, representing a wide range of clay content (3-49%). The results showed that soil physical properties were greatly modified by RAMEB treatment. Analysis of water vapor adsorption isotherms revealed that RAMEB increased water adsorption and surface area in sandy soils and decreased them in clayey soils. An increase in adsorption energy of water in RAMEB-treated soils indicated that desorption of nonpolar pollutants can be enhanced. Water vapor desorption isotherms showed that the volumes and radii of micropores (nanometers range) increased above 1% RAMEB concentration. The micropores became more rough and complex after RAMEB treatment as deduced from an increase in fractal dimensions. The volume of soil mesopores measured by mercury intrusion porosimetry (micrometers range) gradually decreased in most soils with an increase in RAMEB concentration whereas the average mesopore radius increased, indicating that finer mesopores were blocked by RAMEB. Measurements of the granulometric composition of soils by sedimentation analysis showed that the amount of coarse-size soil fractions increased on the expense of finer fractions due to aggregation of smaller particles. Behavior of the studied soils after RAMEB treatment depended on their clay content and the dose of cyclodextrin. In clay-rich soils, strong interactions of cyclodextrins with the soil solid phase governed the resulting soil properties. In clay-poor soils, the cyclodextrin excess (not interacted with clays) played a dominant role. Modification of surface, pore, and aggregation properties of soils by RAMEB can have a significant effect in soil remediation technologies.     

Studies on dimerisation of tocopherols under the influence of methyl linoleate peroxides

The stability of plant oils is related to the level of polyunsaturated fatty acids and the presence of native antioxidants--especially tocopherols. During storage, lipids or the fat products undergo oxidation and tocopherol dimers and trimers are formed. These compounds possess reducing and antioxidant properties and participate in oxidation clearly inhibiting this process. In the present study, the correlation between levels of peroxides formed during autoxidation of methyl linoleate and simultaneous decomposition of tocopherols was examined. The peroxide value was investigated. Quantities of decomposed tocopherols and formation of their dimers were determined by high-performance liquid chromatography (HPLC). Mass spectrum analysis confirmed thatthe analysed compounds were dimes. Dimerisation of gamma-T begins at the smaller quantity of the methyl linoleate peroxides than dimerisation of delta-T. At the beginning of methyl linoleate autoxidation dimerisation of gamma-T in relation to its loss was smaller. The quantity of gamma-T dimers with ether bonds in total dimers pointed to faster binding of phenoxy radicals than transformation into the phenyl ones. delta-T dimers with phenyl bonds constitute about 65% of the total. The quantity of peroxides in methyl linoleate, necessary for quantitative and qualitative changes of homologous tocopherols, decreased from delta-T to alpha-T.