Dye-Modified, Sonochemically Obtained Nano-SnS2 as an Efficient Photocatalyst for Metanil Yellow Removal.

We investigate the possibility of modification of SnS2 powder through sonochemical synthesis with the addition of an organic ligand. For that purpose, two organic dyes are used, Phenol Red and Anthraquinone Violet. All obtained powders are characterized using XRD, SEM, EDX, FT-IR, and UV-Vis investigations. Synthesized samples showed composition and structural properties typical for sonochemically synthesized SnS2. However, investigation with the Tauc method revealed that SnS2 powder modified with Phenol Red exhibits a significant shift in value of optical bandgap to 2.56 eV, while unmodified SnS2 shows an optical bandgap value of 2.42 eV. The modification of SnS2 powder with Anthraquinone Violet was unsuccessful. The obtained nanopowders were utilized as photocatalysts in the process of Metanil Yellow degradation, revealing that SnS2 modified with Phenol Red shows about 23% better performance than the unmodified one. The mean sonochemical efficiency of the performed synthesis is also estimated as 9.35 µg/W.

Comparison of Microstructure, Texture, and Mechanical Properties of TZ61 and AZ61 Mg Alloys Processed by Differential Speed Rolling.

In this work, the comparison of microstructure, texture, and mechanical properties of the newly developed TZ61 (Mg-6Sn-1Zn) alloy with the commercially available AZ61 (Mg-6Al-1Zn) has been presented. Both analyzed Mg alloys were processed by conventional symmetric and asymmetric rolling (i.e., Differential Speed Rolling-DSR). The microstructure and texture were examined by EBSD and XRD, whereas the mechanical behavior was investigated by uniaxial tensile tests. DSR processing led to more effective grain refinement of both TZ61 and AZ61 sheets. However, a high fraction of Mg2Sn phase precipitates in the TZ61 sheets hindered grain growth what resulted in their smaller grain size as compared to AZ61 sheets. DSR processing lowered also the basal texture intensity in the TZ61 and AZ61 sheets. A unique basal poles splitting was observed for the as-rolled TZ61 alloy, while AZ61 alloy exhibited a typical single-peak basal texture. Finally, the reduced grain size and weakened basal texture by DSR processing caused increase of plasticity of the annealed TZ61 and AZ61 sheets. Nevertheless, the annealed AZ61 sheets showed higher uniform elongation and strength (as compared to TZ61 ones), which has been attributed to their significantly lower texture intensity and greater ability to strain hardening.

Analysis of the Morphology and Structure of Carbon Deposit Formed on the Surface of Ni3Al Foils as a Result of Thermocatalytic Decomposition of Ethanol.

This article presents the results of investigations of the morphology and structure of carbon deposit formed as a result of ethanol decomposition at 500 °C, 600 °C, and 700 °C without water vapour and with water vapour (0.35 and 1.1% by volume). scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM) observations as well as energy dispersive X-ray spectrometry (EDS), X-ray diffraction (XRD), and Raman spectroscopic analyses allowed for a comprehensive characterization of the morphology and structure of cylindrical carbon nanostructures present on the surface of the Ni3Al catalyst. Depending on the reaction mixture composition (i.e., water vapour content) and decomposition temperature, various carbon nanotubes/carbon nanofibres (CNTs/CNFs) were observed: multiwalled carbon nanotubes, herringbone-type multiwall carbon nanotubes, cylindrical carbon nanofibers, platelet carbon nanofibers, and helical carbon nanotubes/nanofibres. The discussed carbon nanostructures exhibited nickel nanoparticles at the ends and in the middle part of the carbon nanostructures as catalytically active centres for efficient ethanol decomposition.

Sonochemical preparation of SnS and SnS2 nano- and micropowders and their characterization.

Sonochemical production of tin(II) and tin(IV) sulfides is investigated. Different conditions of syntheses are examined: used solvent (ethanol or ethylenediamine), source of tin (SnCl2 or SnCl4), the molar ratio of thioacetamide to the tin source, and time of sonication. The obtained powders are characterized by the X-ray diffraction method (PXRD), scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), energy-dispersive X-ray spectroscopy (EDX), and the Tauc method. Raman and FT-IR measurements were performed for the obtained samples, which additionally confirmed the crystallinity and phase composition of the samples. The influence of experimental conditions on composition (is it SnS or SnS2), morphology, and on the bandgap of obtained products is elucidated. It was found that longer sonication times favor more crystalline product. Each of bandgaps is direct and most of them show typical values - c.a. 1.3 eV for SnS and 2.4 eV for SnS2. However, there are some exceptions. Synthesized powders show a variety of forms such as needles, flower-like, rods, random agglomerates (SnS2) and balls (SnS). Using ethanol as a solvent led to powders of SnS2 independently of which tin chloride is used. Sonochemistry in ethylenediamine is more diverse: this solvent protects Sn2+ cations from oxidation so mostly SnS is obtained, while SnCl4 does not produce powder of SnS2 but Sn(SO4)2 instead or, at a higher ratio of thioacetamide to SnCl4, green clear mixture.

Microstructure, Texture and Mechanical Properties of Mg-6Sn Alloy Processed by Differential Speed Rolling.

The effect of shear deformation introduced by differential speed rolling (DSR) on the microstructure, texture and mechanical properties of Mg-6Sn alloy was investigated. Mg-6Sn sheets were obtained by DSR at speed ratio between upper and lower rolls of R = 1, 1.25, 2 and 3 (R = 1 refers to symmetric rolling). The microstructural and textural changes were investigated by electron backscattered diffraction (EBSD) and XRD, while the mechanical performance was evaluated based on tensile tests and calculated Lankford parameters. DSR resulted in the pronounced grain refinement of Mg-6Sn sheets and spreading of basal texture as compared to conventionally rolled one. The average grain size and basal texture intensity gradually decreased with increasing speed ratio. The basal poles splitting to transverse direction (TD) or rolling direction (RD) was observed for all Mg-6Sn sheets. For the as-rolled sheets, YS and UTS increased with increasing speed ratio, but a significant anisotropy of strength and ductility between RD and TD has been observed. After annealing at 300 °C, Mg-6Sn sheets became more homogeneous, and the elongation to failure was increased with higher speed ratios. Moreover, the annealed Mg-6Sn sheets were characterized by a very low normal anisotropy (0.91-1.16), which is normally not achieved for the most common Mg-Al-Zn alloys.

The Effect of Oxygen Partial Pressure on Microstructure and Properties of Fe40Al Alloy Sintered under Vacuum.

This paper presents the results of studies on the influence of oxygen partial pressure (vacuum level in the chamber) on the properties of FeAl intermetallics. One of the problems in the application of classical methods of prepared Fe-Al intermetallic is the occurrence of oxides. Applying a vacuum during sintering should reduce this effect. In order to analyze the effect of oxygen partial pressure on sample properties, five samples were processed (by a pressure-assisted induction sintering-PAIS method) under the following pressures: 3, 8, 30, 80, and 300 mbar (corresponding to oxygen partial pressures of 0.63, 1.68, 6.3, 16.8, and 63 mbar, respectively). The chemical and phase composition, hardness, density, and microstructure observations indicate that applying a vacuum significantly impacts intermetallic samples. The compact sintered at pressure 3 mbar is characterized by the most homogeneous microstructure, the highest density, high hardness, and nearly homogeneous chemical composition.

Decomposition of Cyclohexane on Ni3Al Thin Foil Intermetallic Catalyst.

Micro-grained thin foils made of Ni3Al intermetallic alloy were fabricated, according to a previously described procedure, and tested as catalyst for decomposition of cyclohexane. The conversion efficiency of the catalyst was evaluated in a synthetic air atmosphere, and found to be as high as 98.7% ± 1.0% at 600 °C and 86.7% ± 3.6% at 500 °C. During the reaction, the growth of carbon nanofibers on the catalysts surface was observed. The chemical and phase composition of the nanofibers was investigated with scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and X-ray diffraction (XRD), finding them to be made of graphitic carbon. Additionally, nanoparticles of nickel appear to be incorporated in the fibers. The obtained material is promising for large scale fabrication in industrial applications because of its high efficiency in the hydrocarbon decomposition, the simple fabrication procedure, and the form of self-supporting foils with the presence of additional carbon nanofibers that increase its efficiency.