The structure and mechanical properties of Cr-based Cr-Ti alloy films

Previous studies have dealt with Cr and its alloy films that exhibit promising characteristics as surface modification layers for antiwear, anticorrosive, and decorative applications. However, the effect of Ti alloying on the structure and mechanical properties of Cr films has not been studied. This work aimed to the structure and mechanical properties of Cr-Ti alloy films in the Cr-rich side. To this end, pure Cr, Cr-6 at.% Ti, Cr-11 at.% Ti, Cr-16 at.% Ti, and Cr-21 at.% Ti alloy films were prepared by magnetron sputtering, and the structure and mechanical properties of the films were evaluated. The results indicated that all the films exhibited a Cr-based growth with body-centered cubic structure, and increasing the Ti content decreased the (110) orientation growth of Cr basis. Ti alloying increased the hardness of the films, while leaded to a monotonic decrease in the modulus of the films. The first-principles method was employed to demonstrate that the reduced modulus was determined by the Ti alloying degree, rather than the orientation evolution of the films. The analysis of H/E value suggested that the wear resistance of the films was improved by Ti alloying. The mechanical properties of present Cr-Ti alloy films, and other Cr-based alloy films or metallic glasses in publications were compared and discussed. We proposed that Ti alloying is a considerable way to explore advanced mechanical properties of Cr-based alloy films.

Ti(IV)-exchanged nano-ZIF-8 and nano-ZIF-67 for Enhanced Photocatalytic Oxidation of Hydroquinone

The metal centres of nano-ZIF-8(Zn) and nano-ZIF-67(Co) were partially exchanged with titanium centres to form bimetallic nZIF-8(Zn/Ti) (52% Ti4+) and nZIF-67(Co/Ti) (38% Ti4+) respectively, for enhanced photocatalytic performance. A morphological and structural analysis by SEM, EDS-Mapping and PXRD showed that the particle size, distribution, and the structural integrity of the Sodalite frameworks of the parent ZIFs were retained during the exchange process to form the new bimetallic Ti-ZIFs. FTIR confirmed that no additional chemical bonds were formed during the process. XPS binding energies confirmed the preservation of the Zn(II), Co(II) and Ti(IV) oxidation states, as well as the Ti-content, consistent with ICP-OES and EDS measurements. The Ti-exchanged ZIFs showed higher activity during the photocatalytic oxidation of hydroquinone in comparison with their parent ZIFs. Their kinetic rates were nearly five times faster than those of the parent ZIFs, with the first-order rate constants k = 0.189 min-1 for nZIF-8(Zn/Ti) and k = 0.139 min-1 for nZIF-67(Co/Ti). These catalysts are efficient, stable, and reusable for three photocatalytic cycles without a significant loss of catalytic activity.

Kinetic study on the reaction between Incoloy 825 alloy and low-fluoride slag for electroslag remelting

A kinetic model for the reactions between the low-fluoride slag CaF2–CaO–Al2O3–MgO–Li2O–TiO2 and Incoloy 825 alloy was proposed based on the two-film theory. The applicability of the model was verified to predict the variation of components in the slag–metal reaction process. The results show that the controlling step of the reaction 4[Al] + 3(TiO2) = 3[Ti] + 2(Al2O3) is the mass transfer of Al and Ti in the liquid alloy and the controlling step of the reactions 4[Al] + 3(SiO2) = 3[Si] + 2(Al2O3) and [Si] + (TiO2) = [Ti] + (SiO2) is the mass transfer of SiO2 in the molten slag. With increasing TiO2 content in the slag from 3.57% to 11.27%, the Al content in the alloy decreased whereas the Ti content increased gradually. The Si content continued to decrease during the slag–metal reaction. Soluble oxygen in the alloy reacts with Al, Ti, and Si, resulting in a decrease of the oxygen content in the alloy. The variations of TiO2 content were in good agreement with the calculated results by the kinetic model whereas the measured results of Al2O3 and SiO2 in the slag were lower than the calculated results, which is mainly due to the volatilization of fluoride.

The Studies on α-Pinene Oxidation over the TS-1. The Influence of the Temperature, Reaction Time, Titanium and Catalyst Content

The work presents the results of studies on α-pinene oxidation over the TS-1 catalysts with different Ti content (in wt%): TS-1_1 (9.92), TS-1_2 (5.42), TS-1_3 (3.39) and TS-1_4 (3.08). No solvent was used in the oxidation studies, and molecular oxygen was used as the oxidizing agent. The effect of titanium content in the TS-1 catalyst, temperature, reaction time and amount of the catalyst in the reaction mixture on the conversion of α-pinene and the selectivities of appropriate products was investigated. It was found that it is most advantageous to carry out the process of α-pinene oxidation in the presence of the TS-1 catalyst with the titanium content of 5.42 wt% (TS-1_2), at the temperature of 85 °C, for 6 h and with the catalyst TS-1 content in the reaction mixture of 1 wt%. Under these conditions the conversion of α-pinene amounted to 34 mol%, and the selectivities of main products of α-pinene oxidation process were: α-pinene oxide (29 mol%), verbenol (15 mol%) and verbenone (12 mol%). In smaller quantities also campholenic aldehyde, trans-pinocarveol, myrtenal, myrtenol, L-carveol, carvone and 1,2-pinanediol were also formed. These products are of great practical importance in food, cosmetics, perfumery and medicine industries. Kinetic studies were also performed for the studied process.

Microstructure and Oxidation Behavior of Fe-25Mn-9Al-8Ni-1C-xTi Alloy Prepared by Vacuum Arc Melting

In this study, Fe-25Mn-9Al-8Ni-1C-xTi alloy (x = 0, 0.1, 0.2, 0.3, 0.4 wt.%) was prepared by vacuum arc melting, and the corresponding microstructure and oxidation behavior at 600 °C were studied. The results show that Fe-25Mn-9Al-8Ni-1C-xTi alloy mainly contains austenite phase, ferrite phase and TiC phase. With Ti content increasing, the austenite phase content decreases, while the contents of ferrite phase and TiC phase increase. The oxidation performance test results show that the addition of Ti element greatly reduces the oxidation weight gain of the alloys at the initial oxidation stage. With the extension of the oxidation time and the further increase of the Ti content, the alloys oxidation weight gain shows a trend of first increasing and then decreasing. When the Ti content is 0.2 wt.%, the oxidation weight gain of this series of alloy reaches the lowest value during the stable oxidation period. Compared with Fe-25Mn-9Al-8Ni-1C alloy, its weight gain per unit area is reduced by 21.1%. Fe-25Mn-9Al-8Ni-1C-xTi alloy oxide layer exhibits a double-layer structure. The outer oxygen layer is mainly loose iron-oxides, while in the inner oxygen layer, the oxides are mainly composed of manganese-oxides and aluminum-oxides, which are relatively dense.

Catching the Main Ethiopian Rift evolving towards plate divergence

Magmatism accompanies rifting along divergent plate boundaries, although its role before continental breakup remains poorly understood. For example, the magma-assisted Northern Main Ethiopian Rift (NMER) lacks current volcanism and clear tectono-magmatic relationships with its contiguous rift portions. Here we define its magmatic behaviour, identifying the most recent eruptive fissures (EF) whose aphyric basalts have a higher Ti content than those of older monogenetic scoria cones (MSC), which are porphyritic and plagioclase-dominated. Despite these differences, calculations highlight a similar parental melt for EF and MSC products, suggesting only a different evolutionary history after melt generation. While MSC magmas underwent a further step of storage at intermediate crustal levels, EF magmas rose directly from the base of the crust without contamination, even below older polygenetic volcanoes, suggesting rapid propagation of transcrustal dikes across solidified magma chambers. Whether this recent condition in the NMER is stable or transient, it indicates a transition from central polygenetic to linear fissure volcanism, indicative of increased tensile conditions and volcanism directly fed from the base of the crust, suggesting transition towards mature rifting.

Characterization of Sn–Sb–Ti Solder Alloy and the Study of Its Use for the Ultrasonic Soldering Process of SiC Ceramics with a Cu–SiC Metal–Ceramic Composite

The aim of this research was to characterize soldering alloys of the type Sn–Sb–Ti and to study the ultrasonic soldering of SiC ceramics with a metal–ceramic composite of the type Cu–SiC. The Sn5Sb3Ti solder exerts a thermal transformation of a peritectic character with an approximate melting point of 234 °C and a narrow melting interval. The solder microstructure consists of a tin matrix, where the acicular constituents of the Ti6(Sb,Sn)5 phase and the sharp-edged constituents of the TiSbSn phase are precipitated. The tensile strength of the soldering alloy depends on the Ti content and reaches values from 34 to 51 MPa. The average strength of the solder increases with increasing Ti content. The bond with SiC ceramics is formed owing to the interaction of titanium, activated by ultrasound, with SiC ceramics, forming the (Ti,Si)6(Sb,Sn)5 reaction product. The bond with the metal–ceramic composite Cu–SiC is formed owing to the solubility of Cu in a tin solder forming two phases: the wettable η-Cu6Sn5 phase, formed in contact with the solder, and the non-wettable ε-Cu3Sn phase, formed in contact with the copper composite. The average shear strength of the combined joint of SiC/Cu–SiC fabricated using the Sn5Sb3Ti solder was 42.5 MPa. The Sn–Sb–Ti solder is a direct competitor of the S-Bond active solder. The production of solders is cheaper, and the presence of antimony increases their strength. In addition, the application temperature range is wider.

Features of trace element composition of beryl from the Uralian Izumrudnye kopi

It was found as a result of SIMS study of beryl with various color zoning from the Uralian Izumrudnye Kopi that the content of a number of trace elements regularly varies to the margin of the crystal regardless of the color nature of the central and marginal crystal parts. The Na, Mn, Ga, Fe and Rb content increases towards the periphery of both crystals forming a U-shaped zoning. This pattern is less pronounced for Ni and Co. The Ti content, on the contrary, decreases towards the crystal margin forming a bell-shaped zoning. The distribution of a number of elements demonstrates another zoning pattern. For the beryl crystal (sample 24), the color saturation and transparency of which increases from a colorless to green-yellow from the center to the periphery of the crystal, the Sc, Cr and V forms U-shaped zoning with an increasing content to the margin of the crystal and Li exhibits a bell-shaped zoning. In transparent beryl crystal with more intense green color in the center (sample 25), the zoning pattern is dramatically distinct: bell-shaped for Sc, Cr and V and U-shaped for Li. The content of each element for both crystals coincides in the marginal zones, which have color comparable in intensity and transparency, despite the diferent color pattern with a sharply contrast¬ing distribution in the central part. In discriminant diagrams proposed for the identifcation of emeralds from various world regions, the composition of beryl from the Uralian Izumrudnye Kopi correspond to the feld of compositions of the Uralian emeralds or is close to them.