Ni Content Research Articles

Improving the Performance of LiNi0.925Co0.065Mn0.01O2 via Ti4+& Nb5+ Co-Modifications.

Ni-rich layer-structured materials are some of the most promising cathodes owing to their attractive reversible capacity and cost-effectiveness. When the Ni content is increased to 90% and higher, mechanical deterioration becomes serious and leads to accelerated cyclic degradation, since removable Li+ is ∼0.85, accompanied by large lattice variation during operation. Here, we investigate the influences of Ti4+ bulky substitution, Nb5+ surface treatment, and their coutilization on the behavior of LiNi0.925Co0.065Mn0.01O2 (NCM92). In contrast to the limited positive effects of monousage, the coutilization of Ti4+ and Nb5+ obviously suppresses particles' pulverization, relying on their synergistic effects of the shape of lattice variation and the protection of a tough shell layer. As a result, Ti & Nb-LiNi0.925Co0.065Mn0.01O2 (TiNb-NCM92) presents the best capacity retention, as high as 90.2% after 300 cycles, much higher than NCM92 (49.0%), Ti-NCM92 (76.3%), and Nb-NCM92 (72.4%). Our approaches demonstrate that the serious mechanical challenges of ultrahigh nickel cathodes could be alleviated by various remedies coutilized together.

Degradation of toxic components in kitchen waste during hydrothermal carbonization process

Hydrothermal carbonization (HTC) is a promising technique for kitchen waste (KW) disposal. However, KW may contain heavy metals (HMs), aflatoxin, nitrites and sulfites, posing risk for hydrochar utilization. In order to clarify the migration of these toxic components during hydrochar formation process, 7 kinds of kitchen wastes were adopted to carry out HTC experiments at 180–240 °C. Concentration detections results showed that Fe, Mn, Cr, Ni, Cu, and Zn contents were relatively high with a range of 30–2500 mg/kg in KW feedstocks. After HTC treatment, Fe, Cr, Cu were mainly (>80 %) enriched in hydrochar, the enrichment factors of Mn, Ni, Zn was almost above 50 %. From the perspective of species and valence distributions, Mn, Fe, Ni, and Zn in hydrochar were below moderate risk level. No aflatoxin was detected in hydrochar, because AFB1 and AFB2 can be completely degraded into organic acids in the HTC environment at 180 °C. Part benzene rings in aflatoxin were reduced and the C-C bonds were further broken, the C-O bonds were oxidized to produce carboxylic acids. Some benzene rings in aflatoxin remained to form organic acids with aromatic structures. NO2− and SO32- ions with strong ecotoxicity were mostly converted into NO3− and SO42- and flowed into the liquid phase. Some NO2− ions were also converted to and ammonia N and pyridine N; some SO32- ions were converted to sulfonic and sulfinic acid organics, which were successively transformed into sulfonyl/sulfinyl and sulfone/sulfoxide organics. The above findings are of great significance for the transformation mechanism of toxic substances in HTC environment and environment-friendly utilization of hydrochar.

Understanding the Self‐Reconfiguration Properties of a Novel Spinel‐Type High‐Entropy Catalyst

AbstractHigh‐entropy oxides (HEOs), known for their excellent thermodynamic stability due to their high‐entropy effect. In this study, high‐entropy (NixAlCoCrMn)3O4 oxides of spinel structure were synthesized by sol‐gel method. This HEO has a self‐reconfiguration properties in the reaction, and its internal Ni and Co ions exsolve to form a uniformly dispersed NiCo alloy on the surface. The increase of Ni content promotes the exsolution of Ni and Co ions from the interior of the spinel. The high‐entropy with a large number of oxygen vacancies not only possesses a stable structure to limit the migration of NiCo alloys, but also enhances the hydrogen overflow. In the CO methanation reaction, it has 99 % CO conversion with 87 % methane selectivity within 400 °C, and it is stable in the long‐term test. This work provides a new idea for exploring the use of high‐entropy materials to improve thermal catalytic activity and stability.

New insights from crystallography into the effect of Ni content on ductile-brittle transition temperature of 1000 MPa grade high-strength low-alloy steel

The significant effect of Ni content (0.92, 1.94 and 2.94 wt%) on ductile-brittle transition temperature (DBTT) and microstructure in a 1000 MPa grade high-strength low-alloy (HSLA) steel was studied. Using scanning electron microscopy (SEM), electron backscatter diffraction (EBSD), transmission electron microscopy (TEM), Charpy impact test and low-temperature tensile test to study the fundamental reasons for the effect of Ni content on toughness. The results indicated that increasing the Ni content can reduce the DBTT of HSLA steel and improve the impact toughness at low temperatures. EBSD data post-processing analysis revealed that the key reason for the increase in low-temperature toughness is the refinement of the microstructural crystallographic structure, specifically the significant increase in the boundary density of the block and packet. With the increase of Ni content, the density of grain boundary with an orientation difference greater than 5° between two adjacent {110} crystal planes was higher, which can form a higher density of dislocation pile-up group, thus better reducing local stress concentration. Meanwhile, the stacking fault energy (SFE) increases with the increase of Ni content, which made the screw dislocation more prone to cross slip at low temperature, resulting in an increase in plasticity at low temperatures. These observed phenomena and reasons provided a theoretical explanation for the role of Ni content in reducing DBTT and enhancing the toughness of the core in heavy gauge plates.

INFLUENCE OF Ni CONTENT OF ELECTRODEPOSITED Pd-Ni ALLOY COATINGS ON THEIR ELECTROCATALYTIC ACTIVITY IN ALKALINE MEDIUM

The influence of the Ni content (1.4 - 9.0 wt. %) in electrodeposited Pd-Ni alloy coatings on the rate of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in an alkaline media was investigated. Electrocatalytic activity of the electrodeposited layers towards methanol oxidation reaction (MOR) was also studied. The composition and surface morphology of the samples were characterized by energy dispersive spectroscopy (EDS) and scanning electron microscopy (SEM). The crystal structure of the Pd-Ni alloys was examined by X-ray diffraction (XRD). Electrochemical experiments were performed by cyclic voltammetry (CV). The presence of concentration ranges with respect to the Ni content is shown, wherein the electrocatalytic activity of the Pd-Ni alloy towards HER, OER and MOR is higher than that of pure Pd.

Formation Characteristics of Pt-Ni Alloy Nanoparticles Fabricated by Nanolamination of Atomic Layer Deposition in Hydrogen.

Forced-flow atomic layer deposition nanolamination is employed to fabricate Pt-Ni nanoparticles on XC-72, with the compositions ranging from Pt94Ni6 to Pt67Ni33. Hydrogen is used as a co-reactant for depositing Pt and Ni. The growth rate of Pt is slower than that using oxygen reactant, and the growth exhibits preferred orientation along the (111) plane. Ni shows much slower growth rate than Pt, and it is only selectively deposited on Pt, not on the substrate. Higher ratios of Ni would hinder subsequent stacking of Pt atoms, resulting in lower overall growth rate and smaller particles (1.3-2.1nm). Alloying of Pt with Ni causes shifted lattice that leads to larger lattice parameter and d-spacing as Ni fraction increases. From the electronic state analysis, Pt 4f peaks are shifted to lower binding energies with increasing the Ni content, suggesting charge transfer from Ni to Pt. Schematic of the growth behavior is proposed. Most of the alloy nanoparticles exhibit higher electrochemical surface area and oxygen reduction reaction activity than those of commercial Pt. Especially, Pt83Ni17 and Pt87Ni13 show excellent mass activities of 0.76 and 0.59AmgPt -1, respectively, higher than the DOE target of 2025, 0.44AmgPt -1.

The Effect of Nickel Content and Mechanical Activation on Combustion in the 5Ti + 3Si + <i>х</i>Ni System

Intermetallic alloys were synthesized in the 5Ti + 3Si + xNi system by the method of self-propagating high-temperature synthesis (SHS) and mechanosynthesis. The influence of nickel content on the morphology, size and yield of composite particles after mechanical activation (MA) of mixtures was studied. The dependences of the maximum temperatures and combustion rates, phase composition, morphology and elongation of synthesis products on the nickel content for the initial and MA mixtures are studied. Under the conditions of the experiments conducted in this work, combustion process was able to realize and at the same time the samples burned completely at a nickel content of 10 to 60 wt.% in the 5Ti + 3Si + xNi system. After MA, the samples from the 5Ti + 3Si mixture burned to the end, and during the activation of the 5Ti + 3Si + 40% Ni mixture, mechanochemical synthesis occurred. With increasing nickel content combustion temperature decreases, and combustion velocity behaves nonmonotonically, increases the size of composite particles and decreases the yield of the mixture after MA. MA practically did not affect the maximum combustion temperatures of mixtures of 5Ti + 3Si + xNi. A multiple (from 0.7 to 2.9 cm/s) increase in the burning rate of samples from MA mixtures with an increase in the Ni content from 20 to 30 wt. % was recorded. An increase in the nickel content leads to an increase in the content of triple phases and the amount of melt in the synthesis products of mixtures of 5Ti + 3Si + xNi. Shrinkage of product samples increases with increasing nickel content in the initial mixtures. After MA, the shrinkage of the product samples is replaced by their growth. Explanations of the observed dependencies are proposed.

Mechanisms of Co enrichment in the Zhubu Ni–Co–PGE deposit in the Emeishan LIP, SW China: Constraints from mineral geochemistry and Fe–S isotopes of sulfides

The Zhubu Ni–Co–PGE sulfide deposit in the Permian Emeishan Large Igneous Province (LIP), SW China is hosted by a mafic–ultramafic intrusion that comprises two morphologically distinct ore-forming spaces: a central, layered sequence that represents a magma chamber surrounded by a marginal sub-vertical conduit zone. The marginal conduit zone contains significant Ni–Co–PGE sulfide mineralization, suggesting that high volumes of sulfide-bearing silicate melt flowed through the magma conduit system. Determining the hosts of Co is key to understanding the Co enrichment process in the Zhubu deposit, as well as in the Emeishan LIP as a whole. We assess this here using the geochemistry and Fe–S isotope compositions of sulfides in the Zhubu deposit. Cobalt is mainly concentrated in pentlandite sulfide in the websterite, with Co contents increasing in the order pyrrhotite < chalcopyrite < pyrite < pentlandite < violarite; the abundance of violarite, however, is notably lower than that of the other sulfides. The Co contents of pentlandite, pyrite, and chalcopyrite are negatively correlated with their Ni and Fe contents, suggesting that Co substitutes isomorphically for Ni and Fe in the sulfide structure. The δ56Fe values of sulfides increase in the order pyrrhotite < chalcopyrite < pentlandite < pyrite resulted from kinetic fractionation of Fe isotopes. The δ56Fe values of pentlandite and chalcopyrite in lherzolite are higher than those in websterite, implying that lherzolite and websterite formed in compositionally distinct magmas, Fe isotope compositions become heavier with crystal fractionation. The δ34S values of sulfides increase in the order pyrrhotite < pentlandite < chalcopyrite < pyrite, similar to the fractionation sequence of sulfide melts, suggesting that externally derived S was added to the magma and contributed to its sulfide saturation. The Co contents of chalcopyrite and pyrite vary positively with δ56Fe values, and negatively with δ34S values, indicating that the addition of externally derived S and resulting sulfide segregation were critical to Co enrichment.

Influence of Ni content on electrochemical corrosion and tribological behavior of Cu-10Sn coatings by laser cladding

In this work, Cu-10Sn-xNi (x = 0, 3, 6, 9, and 12 wt%) alloy coatings were prepared using laser cladding technology. The influence of Ni content on the phase composition, microstructure, crystallographic characteristics, microhardness, electrochemical corrosion, dry sliding wear and corrosive wear behavior of the coatings were studied. The results indicated that the coatings formed good metallurgical bond with the substrate. The coatings were composed primarily of the α-Cu matrix and small γ precipitates. The Ni element effectively reduced component segregation, and with the increased of Ni content, the grain size in the coating was significantly refined, resulting in fine equiaxed grains. Under the effect of fine grain strengthening, the Cu-10Sn-12Ni (C12NS) coating achieved a higher microhardness of approximately 222.9 ± 5.3 HV0.2. In the electrochemical corrosion test, the increased in the number of grain boundaries significantly reduced the corrosion resistance of the Cu-10Sn-xNi coatings. The Cu-10Sn-6Ni (C6NS) coating exhibited excellent corrosion resistance, with an Icorr of only 1.37 μA/cm2. The results of the dry sliding wear test showed that under the influence of the hardness gradient between the hard precipitate phase and the soft matrix of the coating, the C6NS coating achieved satisfactory wear resistance with a specific wear rate of 3.30 × 104 μm3/Nm. Meanwhile, due to the good corrosive resistance, the C6NS coating showed the best tribological performance in 3.5 wt% NaCl environment, and the specific wear rate was 1.58 × 104 μm3/Nm.

Exploring the role of trace Indium in enhancing the cyclic stability and initial capacity of Lithium–ion cathodes

Developing Ni content over 80 % in Li–ion cathodes for batteries is crucial for achieving higher energy density. However, these materials suffer from instability and rapid capacity loss during repeated charging and discharging cycles. This is primarily due to unwanted structural changes caused by Ni2+ and Li+ ions mixture within the material. This study presents a novel approach using trace amounts of indium (In) doping to significantly improve the lifespan and capacity retention of high–nickel cathodes, even at high discharge rates. Additionally, our fabrication method is simple and scalable, utilizing calcination at a moderate temperature of 720 °C. The In-doped cathode exhibited impressive performance. For a cathode with 82 % nickel content with 0.1 mol% In dopant, the battery delivers a discharge capacity of 231 mAh g-1 at a low discharge rate (0.1 C) and maintains a remarkable capacity retention of 95.1 % even after 50 cycles. This enhanced performance can be ascribed to two key factors: the formation of radially oriented nanorods and a reduction in the overall pore volume within the material. These features contribute to improved stability and reduced cation mixing, leading to a longer–lasting and more efficient battery.

The role of phase transformation (tetragonal – spinel) on the structural and mechanical properties of Ni doped CuFe2O4

Nano-ferrites of Cu1–xNixFe2O4 (x = 0 to 1 with step 0.2) system was synthesized utilizing the flash auto combustion process annealed at 600oC for 3 h. The structural characterization for synthesized samples was carried out using x-ray Diffraction (XRD), Fourier transition infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The hardness of the prepared material was measured using micro-indentation creep technology. XRD pattern verified the creation of a single-phase cubic spinel structure. The undesired CuO phase forms around \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\:2\ heta\\:={50}^{^\\circ\\:}\\:$$\\end{document}for pure Copper ferrite and decreases with increasing Ni content. The average crystalline size decreases from 27.92 nm to 13.28 nm by doping process from x = 0.2 to x = 1 which retards the growth of crystalline size. FTIR spectra are distinguished by the presence of two prominent absorption bands, ν2 for the octahedral site and ν1 for the tetrahedral site, in the range of approximately 593 and 471 cm− 1, respectively. FTIR analysis verified the formation of the ferrite system’s spinel structure. The TEM images show a nanocrystalline nature with some agglomeration and the crystallites are spherical in shape which their sizes are agrees well with that obtained from XRD measurements. The hardness decreases as the dwell time increases. The hardness and yield strength (Y) values were significantly improved due to the decrease in the crystallite size after Ni doping. The stress exponent (n) value increases by increasing Ni content which means that the mechanical properties improved due to increment of resistance.

Refining Alnico 8 magnets with composition optimization of matrix phase, directional solidification and magnetic field annealing

Optimized shape anisotropy of the Fe-Co rich ferromagnetic (α1) phase and the effective separation of the α1 and α2 phases with maximum magnetization difference—where α2 represents a paramagnetic magnetic phase—are the key parameters for maximizing the magnetic properties of Alnico magnets. In this manuscript, efforts have been undertaken to optimize the shape anisotropy of the α1 phase and increase the difference in magnetization and separation between α1 and α2 phases by fine tuning Al and Ni contents, directional solidification and magnetic field annealing methods. At first, Alnico magnets were fabricated by adjusting the content of α2 phase followed by homogenization, magnetic field annealing at high temperature, and low-temperature tempering. Intrinsic coercivity (Hcj) of ⁓146.0 kA/m, remanence (Br) of ⁓0.90 T and maximum energy density ((BH)max) of 46.02 kJ/m3 are achieved in the magnet with 8.2 wt% Al and 12.8 wt% Ni treated in field of 1.5 T for 10 minutes. At the second stage, the magnet with optimal magnetic properties is directionally solidified to develop columnar grains, and then the α1 phase is grown in the direction of the columnar grains by magnetic field annealing to enhance the (BH)max to 79.8 kJ/m3. The axial ratio of the α1 phase increased significantly with the increase of the grain size, particularly in the directionally solidified magnets. The Curie temperature of the α1 phase is noted near 1150 K, while the Curie temperature of the α2 phase is below 400 K. The magnets demonstrated excellent temperature stability, with magnetic properties decreasing by only 10–12 % at 800 K. These results may pave the way for further development of Alnico magnets specifically for high temperature applications.

Optimization of Ni-Cu binder composition and sintering time for enhanced mechanical properties of Mo alloys via liquid phase sintering

Liquid phase sintering of refractory alloys offers a promising approach to enhance mechanical properties while ensuring cost-effectiveness and near-net shaping capabilities. This study systematically explores the impact of sintering time and Ni-Cu binder composition on densification, shape retention, and mechanical properties of Mo alloys processed via liquid phase sintering. The aim is to identify optimal binder composition and sintering time for low-cost production of dense, near-net-shape Mo alloys with superior mechanical properties. The sinterability of Mo compacts is enhanced as the Ni-Cu ratio increases. However, excessive Ni content induces geometric distortion during sintering. Alloys with Ni-rich binders exhibit two liquids at the sintering temperature, each with differing Mo solubility, resulting in a dual-phase matrix on solidification. Both Cu-rich and Ni-rich binder compositions exhibit brittle δ-MoNi intermetallic compound formation, whose quantity increases with prolonged sintering times. Alloys characterized by low Mo solubility in the matrix, high Mo volume fraction, high Mo grain contiguity, and large dihedral angles demonstrate high structural integrity and resistance to geometric distortion. Conversely, alloys featuring high matrix volume fraction, low grain contiguity, elevated Mo solubility in the binder, and strong Mo-matrix interfaces exhibit enhanced strength, hardness, and ductility. Notably, an alloy with a Ni-Cu ratio of 3:1 sintered for just 30 min at 1420°C demonstrates outstanding mechanical properties—hardness of 410 HV, tensile strength of 920 MPa, and elongation of 9 %—comparable to or better than many previously reported refractory alloys.

The oxidation resistance of Ni nanoparticle incorporated SiOC coating for TiAl alloy

In this work, SiOC coatings incorporated with Ni nanoparticles were fabricated on γ-TiAl alloy by dip-coating. The microstructure and high temperature oxidation behavior of the SiOC-Ni coatings with different Ni contents were investigated. Results showed that the incorporation of Ni nanoparticles improved the oxidation resistance of the SiOC coating at 850 ℃. During thermal exposure to air, the incorporated Ni particles would react with both oxygen and the SiOC coating, forming NiO and Ni2Si, respectively, therefore changing the structure of the SiOC coating. The generation of NiO and Ni2Si is beneficial in reducing the oxygen partial pressure at the coating/substrate interface, thereby facilitating the formation of a protective aluminum oxide layer.

Controlled Compositions in Zn–Ni Coatings by Anode Material Selection for Replacing Cadmium

Cadmium-based coatings have long been used to protect high-strength steel in aerospace, but due to cadmium’s toxic and carcinogenic nature, its use is increasingly restricted. Zinc–nickel coatings, containing 10–14 wt% Ni, offer superior corrosion resistance compared to pure zinc, making them a promising alternative. However, Zn–Ni coatings are prone to cracking, which can compromise their protection. This study investigates how different anode materials influence crack formation and coating properties during electrodeposition. Zinc and nickel anodes produced coatings with consistent thicknesses of 13–15 µm, while 1020 steel and stainless steel resulted in thicker coatings of up to 33 µm. Notably, coatings deposited with nickel anodes demonstrated strong adhesion and consistent interface quality. Zinc anodes achieved a high Ni content of about 13.5 wt%, whereas 1020 steel and stainless steel produced lower Ni content, around 7 wt%. Additionally, zinc and nickel anodes led to fewer defects and minimal porosity, in contrast to the higher porosity observed with 1020 steel and stainless steel anodes. Furthermore, zinc anodes maintained stable voltages (~0.5 V), contributing to more uniform coatings. In terms of corrosion resistance, zinc anodes exhibited a lower corrosion rate of 0.44 mm/year compared to 1.54 mm/year for nickel anodes. This study highlights the importance of anode selection in reducing cracking and optimizing Zn–Ni coatings, presenting them as a safer and more effective alternative to cadmium-based coatings.

Performance enhancement of SAW based hydrogen sensor employing Pd/Ni alloy thin film

Abstract This study focuses on determining the optimized design parameters of palladium/nickel (Pd/Ni) thin film coated surface acoustic wave (SAW) hydrogen (H2) sensors with high sensitivity and fast response by modulating the ratio and thickness of Pd/Ni thin film. The Pd/Ni thin films deposited on the wave propagation path of delay-line patterned SAW sensors had Ni content ranging from 0 to 30 at% and thickness ranging from 20 to 400 nm. A phase discrimination circuit was used to collect the signal of SAW H2 sensor. The experimental results indicated that the response sensitivity of the sensor decreased with the increase of Ni content, while the response time gradually accelerated. Besides, the stability of the sensor deteriorated with increasing thickness, and there existed a non-linear relationship between sensitivity and thickness, and the response time slowed down as the thickness increased. To analyze the SAW sensing mechanism, a theoretical simulation model of the Pd/Ni thin film coated SAW H2 sensor was established using perturbation theory, which was well-validated by experimental results. Considering the requirements of fast response, high sensitivity, and stability of the H2 sensor, the optimal thin film structure parameters were determined as Pd9Ni1 thin film with the thickness of 40 nm.

Prolonged arc accretion during growth of juvenile crust in the Arabian Nubian Shield: Insights from the granitoids of northern Ethiopia

The Arabian Nubian Shield (ANS) is one of the largest juvenile continental crust formed after the Archean. To determine the timing and understand the mechanism of its early crustal growth, we conducted geochronological and geochemical studies on granitoids from northern Ethiopia. A plagiogranite, dated at 929.7 ± 2.2 Ma, represents one of the early granitoids from the ANS. It shows low K2O, TiO2, and REE contents, flat REE pattern and absence of Eu anomaly. Moreover, it exhibits (87Sr/86Sr)i, ƐNd(t) and ƐHf(t) values of 0.70341, +5.0 and +8.4, respectively. Its zircon δ18O value is 4.8‰, lower than the mantle value. These characteristics suggest that it was derived from partial melting of altered oceanic crust. The oxygen fugacity obtained from zircon trace elements is ΔFMQ+1.3, consistent with a subduction setting.Other plutons have much younger ages ranging from 860 to 840 Ma and are mainly medium K, I-type granitoids. These granitoids show low MgO, Ni and Cr contents, low Sr/Y, (La/Yb)N, Nb/Ta and Zr/Sm ratios. They exhibit whole-rock (87Sr/86Sr)i values of 0.70236–0.70304, ƐNd(t) values of 4.2–5.2, ƐHf(t) values of 5.8–7.6 and zircon ƐHf(t) values of 5.5–10.4, slightly lower than coeval depleted mantle. Furthermore, they exhibit fractionated REE patterns, enrichments in LILE and depletion in HFSE. These geochemical features suggest that these granitoids were generated by remelting of arc crust. Compiled data show that the associated basaltic rocks are of arc affinity, which confirms the coeval development of arc magmatism in the southern ANS. Our results suggest that the growth of juvenile crust in the southern ANS started from the early Neoproterozoic and peaked at ca. 880 to 800 Ma, much earlier than those in the northern ANS. The prolonged history accounts for the growth of the vast juvenile crust in the ANS.

Physicochemical, Morphological and Anticorrosive Properties of Electrodeposited ZnNi Alloy Coating

Corrosion in its many forms is a major problem for many types of materials, extending from machining to manufacturing and daily use. In fact, it affects practically all engineering projects, from the biggest to the smallest: energy production, construction, transport, medical sector, electronics, etc. Consequently, corrosion generates both economic and environmental problems. To prevent corrosion and preserve materials' durability, several protection methods can be applied. These included protection by applying a coating on the metal surface. In this context, Zinc based alloy coatings have attracted much interesting scientific community because of their excellent mechanical and anti-corrosive properties. In the present work, ZnNi coatings were electrodeposited on steel substrates using a chloride bath containing ammonium salts. The effect of some experimental parameters, namely, potential and metal ion concentration ratio on the deposition kinetics of ZnNi system as well as on its physicochemical, morphological and anticorrosive properties has been investigated. For this purpose, an appropriate experimental work was performed by using both electrochemical (cyclic voltammetry, chronoamperometry, open circuit potential, potentiodynamic polarization) and nonelectrochemical (SEM-EDX) analysis methods. Based on the obtained results, it has been revealed that simultaneous codeposition of both elements Zn and Ni is possible in our experimental conditions. However, deposition kinetics exhibited a strong dependence on explored parameters. Also, morphological aspect and chemical composition of deposits are strongly influenced by metal ion concentration ratio. Investigation of corrosion behaviour confirms the protective effect of coatings acted as a sacrificial anode. Furthermore, increasing Ni content in the deposits induces a significant enhancement in corrosion resistance. Thus, Zn-Ni alloy coatings prepared from the Ni(II)-rich bath exhibited better corrosion resistance.

Impact of Hf alloying on the functional properties of Ni-Mn-Ga high temperature shape memory alloys

The paper reports on the functional properties and microstructure of polycrystalline Ni-Mn-Ga-Hf high temperature shape memory alloys, in which different amounts of Hf up to 4 at.% are added in substitution of Mn and Ga, while the nominal Ni content is kept constant. The increase in the amount of Hf promotes a decrease in the valence electron concentration (e/a), tetragonality (c/a) of the martensitic unit cell, and martensitic transformation temperatures, as well as a significant decrease of the transformation hysteresis. The non-modulated tetragonal martensite, typical of Ni-Mn-Ga high temperature shape memory alloys, is formed in all the alloys studied here, though the alloy with 4 at.% of Hf also contains a small fraction of modulated 14M martensite. Hf addition improves the thermomechanical response of the alloys under compressive stress up to 300 MPa and leads to nearly closed cycles with minimal irrecoverable strain and low hysteresis (8 K) for the alloys with 3 and 4 at.% of Hf. These alloys also demonstrate excellent stability under repetitive thermal cycling and little change upon aging at 870 K. A second phase rich in Hf and Ni starts to precipitate at 1 at.% of Hf addition and its volume fraction experiences an abrupt and progressive increase for higher Hf contents. The structure of the second phase looks like the usual f.c.c. γ phase reported in other Ni-Mn-Ga-based alloys, but it has a double lattice parameter. Two structural models based on the A6 face-centered tetragonal unit cell with space group I4/mmm (No. 139), equivalent to the double f.c.c. lattice, are proposed for this new phase.

Influence of Ni substitution on Structural, Optical, magnetic and transport properties of Mn0.5-xNixZn0.4Cu0.1Fe1.95Al0.05O4

A series of spinel ferrites Mn0.5-xNixZn0.4Cu0.1Fe1.95Al0.05O4 have been prepared by auto-combustion technique. X-ray diffraction (XRD) and Field Emission Scanning Electron Microscopy (FESEM) have been used for structural and morphological investigations. The XRD patterns confirm the formation of cubic spinel structure of ferrites. The lattice constants decrease with the increase of Ni contents due to the smaller ionic radii of Ni2+ compared to Mn2+ as well as particle size decreases. Density is increased and porosity is decreased with the increase of Ni contents in the samples due to the higher atomic weight of Ni2+ compared to Mn2+. The FESEM analysis reveal that the average size of the irregularly shaped grains increased with Ni contents. The mixed spinel structure is further confirmed by the FTIR spectra, which show a doublet band at about 600 cm−1. The observed optical band gap and the particle size variations are comparable, and the quantum size effect supports this conclusion. The real part of initial permeability and relative quality factor increase with the increase of Ni contents due to increase of density and grain size as well as decrease of porosity. Also, it is found that magnetic loss decreased with the increase of Ni contents. All the samples exhibit ferrimagnetic behavior and the number of Bohr magneton has been calculated for all compositions. The dielectric constant shows large value in the lower frequencies and decreases with frequency shows dispersion due to Maxwell-Wagner space charge polarization. The investigation of electric modulus has demonstrated the existence of the hopping conduction mechanism. The AC conductivity is very low at lower frequency region and very large at higher frequency region which can be explain according to the polaron hopping model of Austin and Mott. The AC conductivity enhances nearly linearly with frequency, suggesting that the mechanism of conduction is due to small polaron hopping, which can be described according to Jonscher’s power law. Also, the effect of grain and grain boundary resistance on transport properties has been investigated using complex impedance analysis and it has been observed that both exhibit an increase trend as the Ni content increases.