Search Results (14)

The microstructure, phase composition, and high-temperature oxidation resistance of Fe-free AlCoCrNiNb_0.2 and AlCoCr_0.5NiNb_0.2 high-entropy alloys (HEAs) were investigated. In the as-cast HEAs, niobium was found to mainly release as a Laves phase in the interdendritic region, and its solubility in the dendrites of the BCC solid solution was about 2 at.%. Both samples exhibited parabolic behavior during 100 h oxidation at 1000 °C and 1100 °C. The AlCoCrNiNb_0.2 alloy demonstrated higher resistance to high-temperature oxidation compared to AlCoCr_0.5NiNb_0.2. The specific weight changes after 100 h of isothermal holding at 1000 °C and 1100 °C were 0.65 mg/cm² and 1.31 mg/cm², respectively, which are superior compared to the Fe-containing HEAs. Cr was revealed to play an important role in the oxidation behavior of the HEAs, decreasing the parabolic oxidation rate constant and increasing the activation energy of the oxidation process in the alloys. Full article

The effects of micro-alloying gamma titanium aluminide (γ-TiAl) with niobium (Nb) using a laser melt pool as a melting pot are reported. The Optomec LENS machine was used to carry out the laser in situ alloying experiments where Nb, ranging from 6 to 10 (at. %), was added to the stable binary γ-TiAl alloy. The results of this study concluded that when a stable binary γ-TiAl alloy is micro-alloyed with Nb, there is a definite microstructural transformation, anneal twinning, promotion, and retardation of aluminium solubility in the dual and pure γ phases, respectively. Twinning in the as-built in situ alloyed ternary Ti–48Al–xNb was for the first time reported in this study. It was observed that 6 at. % Nb promoted twinning in the as-built sample, which inferred that the sample might have room temperature ductility. In fact, it was shown that the twins formed in the as-built sample dissipated with the addition of Nb. A heat treatment temperature of 1200 °C promoted anneal twinning only in the binary alloy, as confirmed by XRD data. Meanwhile, this twinning was absent in all the ternary alloys when they were heat treated to a temperature of 1200 °C. Anneal twinning was confirmed only for the alloy containing 8 Nb (at. %) at 1400 °C. Stalk faults, dislocations, and dislocation pile-ups were observed in the α₂ phase of the alloys. Aluminium solubility was seen to increase in the α₂ + γ (±49 at. %) phase alloy and sharply decrease in the pure γ (>49 at. %) phase alloys. Most importantly, this study determined that the laser in situ alloying process was highly exothermic. The heat gained by the reaction was found to increase with the increase in niobium content. Full article

The results of a study of heavy implantation of a LiNbO₃ crystal with iron ions are reported for the first time. The X-cut LiNbO₃ substrate was implanted with 40-keV Fe⁺ ions to the fluence of 1.5·10¹⁷ ions/cm². The sample reveals pronounced ferromagnetic properties at room temperature. However, the ferromagnetic response observed in the iron-implanted LiNbO₃ differs from the magnetic behavior of other oxides implanted with iron ions under the same conditions. This difference occurs from the unusual magnetic phase composition of the implanted surface layer of the LiNbO₃ in which the iron implant precipitates in the form of the nanoscale alloy of metallic iron with niobium. Based on Mössbauer spectroscopy data, we estimated the Nb content in the ion-synthesized nanosized alloy as ~12 at.%, which is much higher than the solid solubility limit of Nb in bulk Fe. Full article

Metal additive processing in polymer: fullerene bulk heterojunction systems is recognized as a viable way for improving polymer photovoltage performance. In this study, the effect of niobium (Nb) metal nanoparticles at concentrations of 2, 4, 6, and 8 mg/mL on poly(3-hexylthiophene-2,5-diyl) (P3HT)-6,6]-phenyl C61-butyric acid methyl ester (PCBM) blends was analyzed. The effect of Nb volume concentration on polymer crystallinity, optical properties, and surface structure of P3HT and PCBM, as well as the enhancement of the performance of P3HT:PC61BM solar cells, are investigated. Absorption of the P3HT:PC61BM mix is seen to have a high intensity and a red shift at 500 nm. The reduction in PL intensity with increasing Nb doping concentrations indicates an increase in PL quenching, suggesting that the domain size of P3HT or conjugation length increases. With a high Nb concentration, crystallinity, material composition, surface roughness, and phase separation are enhanced. Nb enhances PCBM’s solubility in P3HT and decreases the size of amorphous P3HT domains. Based on the J–V characteristics and the optoelectronic study of the thin films, the improvement results from a decreased recombination current, changes in morphology and crystallinity, and an increase in the effective exciton lifespan. At high doping concentrations of Nb nanoparticles, the development of the short-circuit current (J_SC) is associated with alterations in the crystalline structure of P3HT. The highest-performing glass/ITO/PEDOT:PSS/P3HT:PCBM:Nb/MoO₃/Au structures have short-circuit current densities (J_SC) of 16.86 mA/cm², open-circuit voltages (V_OC) of 466 mV, fill factors (FF) of 65.73%, and power conversion efficiency (µ) of 5.16%. Full article

Commercial niobium and synthesized zirconium phosphates were tested as water-tolerant heterogeneous acid catalysts in the hydrothermal conversion of different bio-based substrates. Different acid-catalyzed reactions were performed using biomass-derived model compounds and more complex real lignocellulosic biomasses as the substrate. The conversion of glucose and cellulose was preliminarily investigated. Then, a wide plethora of raw lignocellulosic biomasses, such as conifer wood sawdust, Jerusalem artichoke, sorghum, miscanthus, foxtail millet, hemp and Arundo donax, were valorized towards the production of water-soluble saccharides, 5-hydroxymethylfurfural (HMF), levulinic acid (LA) and furfural. The different catalytic performances of the two phosphates were explained on the basis of their acid features, total acidity, Brønsted/Lewis acid sites ratio and strength. Moreover, a better insight into their structure–acidity relationship was proposed. The different acid properties of niobium and zirconium phosphates enabled us to tune the reaction towards target products, achieving from glucose maximum HMF and LA yields of 24.4 and 24.0 mol%, respectively. Remarkably, when real Jerusalem artichoke biomass was adopted in the presence of niobium and zirconium phosphate, maximum yields of furanic compounds and cellulose-derived sugars of 12.7 and 50.0 mol%, respectively, were obtained, after only 1 h of reaction. The synthesized hydrolysates, which were found to be rich in C5 and C6 carbohydrates, can be better exploited for the cascade production of more added-value bio-products. Full article

In order to realize sustainable development, it is beneficial to explore an appropriate process to recover the radionuclides contained in tantalum-niobium slag. By micro-mineralogical analysis and roasting experiments, the effect of uranium-thorium leaching from a refractory tantalum-niobium slag is investigated. The uranium and thorium content in the slag is 2.26 × 10³ mg/kg and 7.84 × 10³ mg/kg, which have large recovery value. As the surface area and pore size of the slag are very small, the leaching agent cannot fully penetrate the particles. Various methods of characterization are used to analyze the mineralogical properties of roasted slag at different temperatures. The leaching ratio of U-Th is 90.84% and 96.62% at the optimum roasting temperature of 500 °C, which are about 39% and 27% higher than original samples. The oxidants Fe³⁺, O₂ and Mn can also promote the conversion of insoluble U(IV) to soluble U(VI). Roasting reduces the content of organic C and S, thereby preventing reduction of U(VI), and increasing pore size as well as specific surface area also promote radionuclide leaching. Thus, the roasting method at 500 °C can destroy the surface wrapping structure of radionuclides, reduce the internal density of minerals, and improve uranium-thorium leaching ratio significantly. It is of great practical significance to reduce the radioactive hazard of waste tantalum-niobium slag and to strengthen the sustainable utilization of resources by suitable process improvement techniques. Full article

The influence of the nickel content and cooling rate on niobium nitride precipitation in as-cast stainless steels were analysed. Niobium microalloying is important for mechanical properties and the prevention of intergranular corrosion in stainless steels. However, coarse precipitates can negatively affect steel properties. The precipitation of NbN depends on thermodynamic conditions, which are dictated by the chemical composition and temperature. The thermodynamic computations were used to estimate niobium nitride precipitation. Additionally, segregation models were used to predict precipitation. Three steel batches with different nickel contents (9 wt.%, 4.7 wt.%, and 0.16 wt.%) were prepared in an induction furnace and cast into sand moulds. The polished and etched samples were examined with an optical microscope, followed by a more detailed examination using a scanning electron microscope. An automatic scanning electron microscope analysis of the niobium particles was performed to obtain particle number and size distribution. Primary niobium carbonitrides, eutectic phases, and heterogenous nucleations on MnS inclusions were observed. As the proportion of nickel in the solution decreased, the solubility of nitrogen in the melt increased, which is manifested by a lower formation of primary and eutectic niobium carbonitrides, while MnS non-metallic inclusions played an important role in the heterogeneous nucleation. Full article

Because of their superior mechanical performance at ultra-high temperatures, refractory niobium–silicon-based alloys are attractive high-temperature structural alloys, particularly as structural components in gas turbine engines. However, the development of niobium–silicon-based alloys for applications is limited because of the trade-off between room temperature fracture toughness and high-temperature strength. Here, we report on the fabrication of a Nb-18Si alloy with dispersion of hafnium carbide (HfC) particles through selective laser melting (SLM). XRD and SEM-BSE were used to examine the effects of scanning speed on the microstructure and the phase structure of the deposited Nb-18Si-5HfC alloy. The results show that when the scanning speed rises, the solid solubility of the solid solution improves, the interlamellar spacing of eutectics slowly decrease into nano-scale magnitude, and the corresponding hafnium carbide distribution becomes more uniform. We also discover the hafnium carbide particles dispersion in the inter-lamella structure, which contributes to its high fracture toughness property of 20.7 MPa∙m^1/2 at room temperature. Hardness and fracture toughness are simultaneously improved because of the control of microstructure morphology and carbide distribution. Full article

The microstructure, isothermal oxidation, and hardness of the Nb-23Ti-5Si-5Al-5Hf-5V-2Cr-2Sn alloy and the hardness and Young’s moduli of elasticity of its Nb_ss and Nb₅Si₃ were studied. The alloy was selected using the niobium intermetallic composite elaboration (NICE) alloy design methodology. There was macrosegregation of Ti and Si in the cast alloy. The Nb_ss, αNb₅Si₃, γNb₅Si₃, and HfO₂ phases were present in the as-cast or heat-treated alloy plus TiN in the near-the-surface areas of the latter. The vol.% of Nb_ss was about 80%. There were Ti- and Ti-and-Hf-rich areas in the solid solution and the 5-3 silicide, respectively, and there was a lamellar microstructure of these two phases. The V partitioned to the Nb_ss, where the solubilities of Al, Cr, Hf, and V increased with increasing Ti concentration. At 700, 800, and 900 °C, the alloy did not suffer from catastrophic pest oxidation; it followed parabolic oxidation kinetics in the former two temperatures and linear oxidation kinetics in the latter, where its mass change was the lowest compared with other Sn-containing alloys. An Sn-rich layer formed in the interface between the scale and the substrate, which consisted of the Nb₃Sn and Nb₆Sn₅ compounds at 900 °C. The latter compound was not contaminated with oxygen. Both the Nb_ss and Nb₅Si₃ were contaminated with oxygen, with the former contaminated more severely than the latter. The bulk of the alloy was also contaminated with oxygen. The alloying of the Nb_ss with Sn increased its elastic modulus compared with Sn-free solid solutions. The hardness of the alloy, its Nb_ss, and its specific room temperature strength compared favourably with many refractory metal-complex-concentrated alloys (RCCAs). The agreement of the predictions of NICE with the experimental results was satisfactory. Full article

To realize light-weight materials with high strength and ductility, an effective route is to incorporate strong and stiff metallic elements in light-weight matrices. Based on this approach, in this work, magnesium–iron (Mg-Fe) composites were designed and characterized for their microstructure and mechanical properties. The Mg-Fe binary system has extremely low solubility of Fe in the Mg-rich region. Pure magnesium was incorporated with 5, 10, and 15 wt.% Fe particles to form Mg-Fe metal–metal composites by the disintegrated melt deposition technique, followed by hot extrusion. Results showed that the iron content influences (i) the distribution of Fe particles in the Mg matrix, (ii) grain refinement, and (iii) change in crystallographic orientation. Mechanical testing showed that amongst the composites, Mg-5Fe had the highest hardness, strength, and ductility due to (a) the uniform distribution of Fe particles in the Mg matrix, (b) grain refinement, (c) texture randomization, (d) Fe particles acting as effective reinforcement, and (e) absence of deleterious interfacial reactions. Under impression creep, the Mg-5Fe composite had a creep rate similar to those of commercial creep-resistant AE42 alloys and Mg ceramic composites at 473 K. Factors influencing the performance of Mg-5Fe and other Mg metal–metal composites having molybdenum, niobium, and titanium (elements with low solubility in Mg) are presented and discussed. Full article

Dual phase (DP) steels are widely applied in today’s automotive body design. The favorable combination of strength and ductility in such steels is in first place related to the share of ferrite and martensite. The pronounced work hardening behavior prevents localized thinning and allows excellent stretch forming. Niobium microalloying was originally introduced to dual phase steel for improving bendability by refining the microstructure. More recently developed “high ductility” (HD) DP steel variants provide increased drawability aided by a small share of austenite retained in the microstructure. In this variant niobium microalloying produces grain refinement and produces a dispersion of nanometer-sized carbide precipitates in the steel matrix which additionally contributes to strength. This study investigates the microstructural evolution and progress of niobium precipitation during industrial processing of high-ductility DP 980. The observations are interpreted considering the solubility and precipitation kinetics of niobium. The influences of niobium on microstructural characteristics and its contributions to strength and formability are discussed. Full article

Two high Nb-containing TiAl alloys, Ti46.6Al7.5Nb0.5Si0.2B (Alloy A) and Ti46.1Al7.4Nb5C0.5Si0.2B (Alloy B), were prepared by graphite mold casting. As-cast microstructures of the two alloys were characterized to clarify the effect of carbon addition. The results show that 5 at.% carbon addition can change the primary solidification phase from β phase to α phase. The as-cast microstructure of Alloy A consists of a fully α₂ + γ lamellar structure and interdendritic eutectic silicide with a volume fraction of 2.3%. However, in Alloy B, the lamellar structure only forms in the dendritic stem and the massive γ is observed in the interdendritic regions. Two types of carbides, ${\mathrm{Ti}}_2\mathrm{AlC}$ and TiC, are produced in Alloy B. A large number of randomly distributed primary ${\mathrm{Ti}}_2\mathrm{AlC}$ particles with volume fraction of 14.9% are observed in both the dendritic and interdendritic regions. Irregularly shaped TiC remains inside of the large ${\mathrm{Ti}}_2\mathrm{AlC}$ particle, suggesting TiC carbides transformed to ${\mathrm{Ti}}_2\mathrm{AlC}$ during cooling. The addition of carbon also changes the morphology of the silicides from a eutectic structure to a blocky structure in the massive γ matrix or at the interface of the Ti₂AlC and the γ matrix. High level of niobium greatly increases the solid solution limit of carbon, since C content in the matrix is much higher than the solid solubility of that in the TiAl binary system. The hardness of the matrix increases from 325 HV to 917 HV caused by the addition of carbon. Full article

Eudialyte, a sodium rich zirconosilicate, is one of the promising sources for REEs (rare earth elements), particularly for HREEs + Y (heavy rare earth elements and yttrium). The key challenge in hydrometallurgical processing is the prevention of silica gel formation and REE separation from resulting multi-element leach solutions. This study deals with the selective extraction of REE from eudialyte concentrate by selective roasting. In this method, metal ions are converted into sulfates, followed by the decomposition of non-REE sulfates in a roasting step and the water leaching of the calcine. The effect of acid addition, roasting temperature, roasting time, pulp density and leaching time is studied. For sufficient conversion of REEs into sulfates, sulfuric acid is added in excess. At a roasting temperature of ≥750 °C sulfates of zirconium, hafnium, niobium, aluminum and iron decompose into sparingly soluble compounds, while REE and manganese sulfates remain stable up to a roasting time of 120 min. The silica present in the calcine is found to be metastable even after roasting. The amount of leached Si⁴⁺ is dependent predominantly on the pH value of the leaching medium. Applying the method, REEs can be efficiently separated from zirconium, hafnium, niobium, aluminum and iron. However, only diluted solutions can be produced. Water leaching of calcine at high solid/liquid ratios causes REE losses resulting from formation of double sulfates and gypsum. The acid excess removed from the reaction mixture in the roasting stage can be simply recovered by treatment of the gas phase. Full article

Irreversible hydrocolloids (IR) is a dental impression material commonly used in Brazilian and European dental practice because it is inexpensive, easy to handle, has good reproductive detail and is comfortable for the patient. This research aimed to analyze the chemical composition of eight different IRs for dental use. A sample of 0.2 g was weighed and transferred to a Teflon beaker moistened with drops of distilled or deionized water; 5 mL of nitric acid was added until total solubility of the sample; the solution was transferred to a 100 mL volumetric flask, the volume was filled with distilled or deionized water and homogenized. Thirty-five chemical elements were found: Lithium, Beryllium, Boron, Sodium, Magnesium, Aluminum, Silicon, Phosphorus, Potassium, Titanium, Manganese, Cobalt, Nickel, Vanadium, Zinc, Rubidium, Arsenic, Iron, Copper, Strontium, Yttrium, Zirconium, Niobium, Molybdenum, Ruthenium, Cadmium, Tin, Antimony, Barium, Lanthanum, Cerium, Mercury, Lead, Thorium and Uranium. Only one of the samples contained no Nickel, Antimony and Lead; and Arsenic and Uranium were found in 2 samples. This study provided evidence of high toxicity of the IR brands, pointing out the need for better quality control of this product, in order to prevent health damage in dentists, prosthesis technicians and patients. Full article