Composition Of Nickel Research Articles

Phase composition and microstructure of intermetallic alloys obtained using electron-beam additive manufacturing

The paper investigates the microstructure and phase composition of nickel- and aluminum-based intermetallic alloys obtained using two-wire electron-beam additive manufacturing (EBAM). Relevance of the research is related to the widespread use of intermetallic alloys based on nickel and aluminum (mainly Ni3Al) in various high-temperature applications and the need to use modern production methods when creating machine parts and mechanisms from these alloys. Using EBAM, the billets from intermetallic alloys with different ratios of the content of main components were obtained. Change in concentrations of the basic elements was carried out varying the ratio of feed rates of nickel and aluminum wires during additive manufacturing in the range from 1:1 to 3:1, respectively. The results of microscopic studies of the obtained alloys showed that, regardless of nickel content, the obtained alloys are characterized by a large–crystalline structure with grain sizes in the range of 100 – 300 μm for alloys with a component ratio of 1:1 and 150 – 400 μm for alloys with a component ratio of 2:1 and 3:1. At the same time, the alloy with an equal content of base components is characterized by more uniform grain and microstructure compared to those with high content of Ni. By changing the concentration ratio of the components, phase composition of the resulting billet can be purposefully controlled. In the case of an “equiatomic” content of the base components in the alloy, a NiAl-based compound with a small phase content based on the intermetallides Ni3Al5 and Ni3Al is formed. At high concent­rations of nickel, the intermetallic Ni3Al phase is formed, and at a component ratio of 3:1, structure of the resulting billet consists mainly of Ni3Al phase and the γ solid substitutional solution based on nickel. The paper demonstrates the possibility of direct production of intermetallic alloys with a given phase composition during electron-beam additive manufacturing.

Assessment of vacancy migration energy in a ternary austenitic steel Fe–Cr-Ni with 16% chromium and 20% nickel composition, using kinetic Monte Carlo method, considering an ordering model via vacancy diffusion mechanism

Assessment of vacancy migration energy in a ternary austenitic steel Fe–Cr-Ni with 16% chromium and 20% nickel composition, using kinetic Monte Carlo method, considering an ordering model via vacancy diffusion mechanism

Impact of mineral and non-mineral sources of iron and sulfur on the metalloproteome of Methanosarcina barkeri.

Methanogens often inhabit sulfidic environments that favor the precipitation of transition metals such as iron (Fe) as metal sulfides, including mackinawite (FeS) and pyrite (FeS2). These metal sulfides have historically been considered biologically unavailable. Nonetheless, methanogens are commonly cultivated with sulfide (HS-) as a sulfur source, a condition that would be expected to favor metal precipitation and thus limit metal availability. Recent studies have shown that methanogens can access Fe and sulfur (S) from FeS and FeS2 to sustain growth. As such, medium supplied with FeS2 should lead to higher availability of transition metals when compared to medium supplied with HS-. Here, we examined how transition metal availability under sulfidic (i.e., cells provided with HS- as sole S source) versus non-sulfidic (cells provided with FeS2 as sole S source) conditions impact the metalloproteome of Methanosarcina barkeri Fusaro. To achieve this, we employed size exclusion chromatography coupled with inductively coupled plasma mass spectrometry and shotgun proteomics. Significant changes were observed in the composition and abundance of iron, cobalt, nickel, zinc, and molybdenum proteins. Among the differences were alterations in the stoichiometry and abundance of multisubunit protein complexes involved in methanogenesis and electron transport chains. Our data suggest that M. barkeri utilizes the minimal iron-sulfur cluster complex and canonical cysteine biosynthesis proteins when grown on FeS2 but uses the canonical Suf pathway in conjunction with the tRNA-Sep cysteine pathway for iron-sulfur cluster and cysteine biosynthesis under sulfidic growth conditions.IMPORTANCEProteins that catalyze biochemical reactions often require transition metals that can have a high affinity for sulfur, another required element for life. Thus, the availability of metals and sulfur are intertwined and can have large impacts on an organismismal biochemistry. Methanogens often occupy anoxic, sulfide-rich (euxinic) environments that favor the precipitation of transition metals as metal sulfides, thereby creating presumed metal limitation. Recently, several methanogens have been shown to acquire iron and sulfur from pyrite, an abundant iron-sulfide mineral that was traditionally considered to be unavailable to biology. The work presented here provides new insights into the distribution of metalloproteins, and metal uptake of Methanosarcina barkeri Fusaro grown under euxinic or pyritic growth conditions. Thorough characterizations of this methanogen under different metal and sulfur conditions increase our understanding of the influence of metal availability on methanogens, and presumably other anaerobes, that inhabit euxinic environments.

Fabrication of an In‐situ Synthesized Porous Silica‐Ruthenium‐Nickel Composite Catalyst for Hydrolysis of Ammonia Borane

AbstractThis work investigated in‐situ synthesis of porous silica‐nickel‐ruthenium composite catalysts for hydrolysis of ammonia borane. The precursors were prepared with an anionic surfactant, sodium dodecyl sulfate (SDS), to form porous structure in the precursor particles, and the precursors was treated in aqueous solution including sodium borohydride and ammonia borane for in‐situ process to parallelly activate and use the catalysts for hydrolysis of ammonia borane. The result of TEM and nitrogen sorption measurements suggested that the primary particle size of the in‐situ synthesized catalysts decrease with increasing the amount of SDS and sodium chloride as the additive for controlling the primary particle size probably because of the effect of sodium ions to inhibit nuclei growth of the primary particles. From the EDS analyses, the composition of active nickel and ruthenium contents increased with increasing the amount of SDS and sodium chloride except for the highest amount of SDS probably because of adsorption of the metal cations with the excess amount of the surfactant anion to decrease the amount of the metal cations including the catalyst. The in‐situ synthesized catalyst including small size primary particles and high nickel and ruthenium content tended to exhibit high activity for hydrolysis of ammonia borane.

Electrodeposition of Non-Noble High-Entropy Alloys for Effective Hydrogen Evolution Electrocatalysts

As society works towards reducing its carbon footprint, various sectors such as energy, steelmaking and fertilizer production have begun to look increasingly towards decarbonization. Hydrogen production through electrolysis, when linked to renewables (solar, wind), provides a promising low-emission alternative as an energy carrier and chemical feedstock. With the decreasing cost of said renewables, greater focus is now on the capital cost of the electrolyser, and particularly the membrane/electrode structures. Conventional Proton Exchange Membrane (PEM) electrolysers rely on the use of electrocatalysts made with expensive noble metals such as platinum, ruthenium, and palladium [1]. Anion Exchange Membrane (AEM) electrolysers present an effective means of alkaline water splitting with low carbon emissions and can effectively utilize non-noble metal electrocatalysts for the Hydrogen Evolution Reaction (HER). A novel class of materials, High-Entropy Alloys (HEAs), made of non-noble metals or with reduced noble metal content have shown great promise as active electrocatalytic materials [2]. HEAs are typically defined as metal alloys made of five or more constituent elements each comprising at least 5% of the total material [3]. Having such a large number of principal alloying elements can lead to enhanced phase stability due to an increased configurational entropy, have unique chemical clustering, and can help prevent degradation of the material in harsh environments [2]. Additionally, the large lattice parameter mismatch between constituent elements can result in a high degree of strain which can help shift electronic states in a way that is favourable to hydrogen electrocatalysis [4]. These properties along with the so called “cocktail effect,” whereby combining multiple elements can result in unexpected synergistic interactions, makes HEAs uniquely suited to electrocatalytic applications [5].In this work, we investigate the electrocatalytic performance of electrodeposited FeNiCoMoW HEAs. The goal is to combine three hyper-d transition metals with two hypo-d transition metals to alter the electronic structure and improve electrocatalytic performance. Using chronoamperometric measurements, the Tafel slopes for FeNiCoMoW HEAs electrodeposited at pH 5, 6 and 7 were determined, with the pH 5 HEA demonstrating the smallest average Tafel slope of approximately 83 mV/dec. Compared to some electrodeposited binary alloys reported on in the literature, this marks an improvement and may be the result of unexpected interactions within the compositionally complex alloy. In the FeNiCoMoW HEA, the magnitude of the Tafel slope increased in tandem with the electrochemically active surface area (ECSA) as determined by Cyclic Voltammetry (CV) which suggests that the composition may be more important for improving performance. As the pH of the electrodeposition solution increased, the amount of cobalt in the as-deposited HEA decreased while the amounts of molybdenum and tungsten remained constant. The composition of nickel and iron appeared to vary inversely, reaching a maximum and minimum respectively at pH 6. From these results it seems that maximizing cobalt content and minimizing nickel content could potentially help to improve HER performance in the FeNiCoMoW system.

Green synthesis and multifunctional properties of Cu/NiO nanocomposites using Commelina benghalensis leaf extract

This study presents the green synthesis and multifunctional properties of Cu/NiO nanocomposites (NCs) fabricated with varying ratios (90:10, 80:20, and 70:30) using Commelina benghalensis leaf extract. X-ray diffraction (XRD) analysis confirmed the polycrystalline nature of the NCs, revealing crystallite sizes of 13.62, 13.22, and 7.14 nm. Scanning electron microscopy (SEM) showed rod-shaped and agglomerated particles with sizes ranging from 17.64 to 22.97 nm. Energy-dispersive X-ray spectroscopy (EDX) verified the elemental composition of copper, nickel, oxygen, and carbon. UV–visible spectroscopy determined the energy band gaps to be in the range of 1.24–1.56 eV. Fourier-transform infrared spectroscopy (FT-IR) indicated the presence of bioactive compounds responsible for the reduction of precursor metal salts. The Cu/NiO NCs exhibited remarkable antimicrobial activity, with the 90:10 ratio showing the highest zones of inhibition at 32.76 ± 0.23 mm, 18.66 ± 0.33 mm, and 14.36 ± 0.32 mm against Bacillus subtilis, Staphylococcus aureus, and Escherichia coli, respectively. Additionally, the 70:30 Cu/NiO NCs demonstrated superior antioxidant activity, with a radical scavenging efficiency of 83.22%, closely approaching that of ascorbic acid (96.98%). Photocatalytic evaluations revealed that the NCs were highly effective in degrading environmental pollutants, achieving 97.69% degradation of malachite green and 96.52% of congo red under UV light irradiation. The novelty of this work lies in the use of Commelina benghalensis leaf extract as a sustainable and eco-friendly reducing and stabilizing agent for synthesizing Cu/NiO NCs, offering a green alternative to conventional methods. The synergistic effects between Cu and NiO in the different compositions (90:10, 80:20, and 70:30) enhanced the overall antimicrobial and photocatalytic activities, highlighting their potential for environmental remediation applications.

Temperature-Dependent Structural Properties of Nickel and Cobalt Selenite Hydrates as Solar Water Evaporators.

Solar water evaporation offers a promising solution to address global water scarcity, utilizing renewable energy for purification and desalination. Transition-metal selenite hydrates (specifically nickel and cobalt) have shown potential as solar absorbers with high evaporation rates of 1.83 and 2.34 kg∙m-2∙h-1, but the reported discrepancy in evaporation rate deserves further investigation. This investigation aims to clarify their thermal stability for applications and determine the underlying mechanisms responsible for the differences. Nickel and cobalt selenite hydrate compositions were synthesized and investigated via thermogravimetric analysis, X-ray diffraction, and Raman spectroscopy to assess their temperature-induced structural and compositional variations. The results reveal distinct phase transitions and structural alterations under various temperature conditions for these two photothermal materials, providing valuable insights into the factors influencing water transportation and evaporation rates.

Synergistic effects of chemical composition on precipitates, dislocations, and mechanical properties of precipitation-strengthened alloys

The properties of materials are intricately dependent on their chemical composition, and microstructures. Achieving a precise modulation in the composition and microstructure of materials to enhance properties significantly is a huge challenge. In this work, we uncovered the effects of nickel and silicon composition on the precipitates, dislocations, and properties of Cu–Ni–Si alloys. The results show that the volume fraction of precipitates increased from 0.84 % to 4.80 % with the increase of Ni and Si contents. The average diameter of the precipitates increased from 6.20 nm to 20.21 nm, and the dislocation density increased from 2.16 × 1013 m−2 to 4.08 × 1015 m−2 concerning the Ni and Si contents. In addition, the dislocation type changes from half-edge dislocation and half-screw dislocation to screw dislocation. The modified WHWA (Williamson Hall-Warren Averbach) method was proved to be the most accurate way of calculating dislocation density. As anisotropy was present in the alloy, adding a dislocation contrast factor and removing some lower-intensity diffraction peaks could further correct the obtained results and reduce the calculation error. Furthermore, the above analysis and findings were employed to design a Cu-3.21Ni-0.66Si alloy with a high yield strength (814 MPa), high ultimate tensile strength (970 MPa), and comparable electrical conductivity of 42.4 % IACS. This work offers a meaningful way to develop precipitation-strengthening alloys.

Improved electrochemical performance of hydrothermally synthesized Zn-Ni-S/rGO nanocomposite as an electrode for supercapacitor application

This present work reports on the hydrothermal synthesis of zinc-nickel sulfide with reduced graphene oxide (Zn-Ni-S/rGO) nanocomposite for supercapacitor applications. The synthesized samples are evaluated using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FE-SEM), and high-resolution scanning transmission electron microscopy (HR-TEM), which are employed to examine the structure, morphology, and chemical composition of the Zn-Ni-S/rGO nanocomposite. The XRD results indicates formation of high crystalline Zn-Ni-S/ rGO nanocomposites. FE-SEM equipped with an EDX spectrum, illustrates a spherical morphology of Zn-Ni-S combined with a thin layer of rGO in the form of composite nature. Furthermore, elemental composition of Zinc, Nickel, Sulfur and Carbon presence in the EDS spectra further supports the formation of Zn-Ni-S/rGO nanocomposite. The electrochemcial properties of ZnS and Zn-Ni-S/rGO nanocomposite are studied through cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy. High specific capacitance of 284 F/g is obtained at 11 mA g−1 current density. The Zn-Ni-S/rGO nanocomposite demonstrates high capacitance retention of 96 % over 3,000 cycles. The potential application of the Zn-Ni-S/rGO nanocomposite as an efficient electrode material for pseudocapacitors is supported by its favourable performance.

THE DESIGN AND CHARACTERIZATION OF MODIFIED POLYTHIOPHENE SUPPORTED PLANT MEDIATED CO-NI BIMETALLIC NANOCOMPOSITES

Ficus mucuso leaf extract was employed as reducing agent in the synthesis of Co-Ni bimetallic nanoparticles (BMNPs) with two precursors namely; Cobalt (ii) nitrate hexahydrate; [CO(NO3)2.6H2O] and nickel (ii) nitrate hexahydrate; [Ni (NO3)2.6H2O]. Afterwards, acid modified polythiophene was synthesized through the in-situ and ex-situ coupling approach. The nanocomposite obtained from the in-situ method was labelled ‘A’ and that of the ex-situ, ‘B’. The in-situ approach was considered to be more appropriate for synthesizing the BMNPs as confirmed by characterization using Fourier Transform Infrared Spectroscopy (FTIR), X-Ray diffraction analysis (XRD), Energy dispersive X-ray (EDX) analysis, Transmission electron microscopy (TEM), Thermogravimetric analysis (TGA) and Scanning electron microscopy (SEM) techniques. The hexagonal cobalt and the cubic nickel were investigated using XRD to determine the particle sizes taking Debye-Scherrer’s equation to be around 14.495nm for sample A and 15.689nm for sample B. This was reported to be responsible for the corresponding intense peak at A over B. The SEM and TEM measurements portray good correlation indicating the presence of agglomerates in sample B. The EDS analysis taken reported a higher weight of the cobalt and nickel compositions in A than in B. TGA explained the higher decomposition rate of B than A. Also, a more pronounced intense peak was observed in A than in B using FTIR technique. This comparison of both samples makes in-situ synthesis unquestionably the best because of its outstanding performance over ex-situ approach. This is the first report of Ficus Mucuso plant extract being used in nanosynthesis.

Calcium-, magnesium-, and yttrium-doped lithium nickel phosphate nanomaterials as high-performance catalysts for electrochemical water oxidation reaction

Abstract Electrochemical water oxidation reaction (WOR) lies among the most forthcoming approaches toward eco-conscious manufacturing of green hydrogen owing to its environmental favors and high energy density values. Its vast commoditization is restricted by high-efficiency and inexpensive catalysts that are extensively under constant research. Herein, calcium, magnesium, and yttrium doped lithium nickel phosphate olivines (LiNi1−x M x PO, LNMP; x = 0.1–0.9; M = Ca2+, Mg2+, and Y3+) were synthesized via non-aqueous sol-gel method and explored for catalytic WOR. Lithium nickel phosphates (LNP) and compositions were characterized via Fourier transform infrared, scanning electron microscopy, X-ray diffraction, and energy dispersive X-ray diffraction techniques for the structural and morphological analyses. Glassy carbon electrode altered with the LNMPs when studied in a standard redox system of 5 mM KMnO4, displayed that yttrium doped LNP, i.e. LNYP-3 exhibits the highest active surface area (0.0050 cm2) displaying the lowest average crystallite size (D avg) i.e. ∼7 nm. Electrocatalytic behavior monitored in KOH showed that LNMP-2 offers the highest rate constant “k o,” value, i.e. 3.9 10−2 cm s−1 and the largest diffusion coefficient “D o,” i.e. 5.2 × 10−5 cm2 s−1. Kinetic and thermodynamic parameters demonstrated the facilitated electron transfer and electrocatalytic properties of proposed nanomaterials. Water oxidation peak current density values were indicative of the robust catalysis and facilitated water oxidation process besides lowering the Faradic onset potential signifying the transformation of less LNP into more conducive LNMP toward water oxidation.

X-ray Fluorescence Analysis of the Elemental Composition of Tungsten, Nickel and Copper

The purpose of this work was to conduct an X-ray fluorescence analysis of the elemental composition of tungsten, nickel and copper metal waste using an Olympus Delta portable spectrometer.Methods. To determine the chemical composition of raw materials, samples of metal waste in the form of copper rods, tungsten rods of various diameters and scraps of nickel plates intended for recycling were examined. To determine the elemental composition of metal waste, the method of X-ray fluorescence analysis (XFA) was chosen. The X-ray fluorescence method is based on the ratio of the intensity of X-ray fluorescence to the concentration of elements in the sample. Samples irradiated with powerful X-ray tube radiation, in response, emit characteristic fluorescent radiation of atoms proportional to their concentration in the sample. This method allows us to qualitatively assess the elemental composition of complex samples without violating their physico-chemical properties with minimal time costs. The Olympus Delta spectrometer was used as an express analyzer of metals and alloys, with the help of which experimental data on the composition of metal waste of tungsten, nickel and copper were obtained.Results. Based on the conducted studies aimed at X-ray fluorescence analysis of the elemental composition of tungsten, nickel and copper metal waste using the Olympus Delta portable spectrometer, it was found that the samples of the studied metal waste correspond to the following grades of alloys: tungsten rod made of tungsten grade VA; nickel plate made of nickel grade PNK-0T1; copper rod made of copper grade M3r.Conclusion. The results obtained will allow further research on their processing by the method of electroerosive dispersion and reuse in the production of heavy tungsten alloys. Renovation of metal waste, including tungsten, nickel and copper metal waste, will contribute to resource conservation, import substitution and ensuring the technological sovereignty of the Russian Federation.

Multicomponent solvent extraction modelling of lithium, cobalt, nickel, and manganese from simulated black mass leachate

The role of lithium-ion batteries in facilitating the global shift towards renewable energy is paramount. Managing the responsible lifecycle of these batteries, including their disposal and recycling at the end of their operational life, holds considerable importance. These practices not only mitigate the environmental impact but also address the supply vulnerability of battery metals sourced from primary natural reserves. The major compositions of batteries, notably lithium, nickel, and cobalt, are typically concentrated within a material known as black mass, a vital commodity in the battery recycling sector. Solvent extraction is a proficient method for the simultaneous recovery of these materials, to produce a feedstock for new battery manufacturing, aligning with the principles of a circular economy. The separation and purification of these metals, while still challenging, are comparatively less difficult than the requirement posed by primary resource extraction. The co-extraction of multiple compositions in a single step holds tremendous potential for reducing the cost associated with the separation process. Nevertheless, this approach is an unconventional solvent extraction method, necessitating advanced multicomponent extraction models. The present study employed the equilibrium status iteration (ESI) model to describe and predict the extraction performance of battery metals in aqueous solutions. This model is instrumental to the design and optimisation of scaled-up solvent extraction facilities. To illustrate the model, ESI was applied to resolve equilibrium data related to a three-stage counter-current extraction scheme. This removes the laborious trial-and-error phase of experimental inquiry when designing the process involving multiple target metals.

Association between nickel exposure and body compositions in the United States: a population-based cross-sectional study

BackgroundIncreasing body fat or decreasing muscle and bone mass were associated with worse health outcomes in the adult population. The effects of nickel exposure on body composition are not known. The aim of the current study was to investigate the relationship between urinary nickel levels and body compositions.Materials and methodsTwo thousand seven hundred sixty-two participants were included in the analysis from the National Health and Nutrition Examination Surveys of 2017–2018 after excluding participants who have missing data on urinary nickel and those with missing all body mass component data. We used weighted generalized linear models to explore the relationship between urinary nickel and body mass components under interpolating missing covariable values. Simultaneously, sensitivity analyses and subgroup analysis were conducted to verify stability of analysis result. Curve fitting and saturation effect analysis were used to explore the possible nonlinear relationship between urine nickel and body compositions.ResultsAmong the 2,762 participants, the average urinary nickel level was 1.58 ug/L. The weighted generalized linear models, the sensitivity analyses and subgroup analyses found no significant linear relationship between urinary nickel and body compositions. For body weight, BMI, TLM, ALM, TRF, TOF and BMC, the urine nickel saturation effect values were 0.76, 0.74, 0.5, 0.67, 0.64, 0.48, and 0.45 ug/L, respectively. For each 1 ug/L rise in urinary nickel levels at levels below the turning point, body weight increases (β = 9.06, 95% CI = 2.75, 15.36, p = 0.01), BMI increases (β = 3.20, 95% CI = 1.36, 5.05, p = < 0.001), TLM decreases (β = -47.39, 95% CI = -97.38, 2.59, p = 0.06), ALM decreases (β = -37.25, 95% CI = -63.25, -11.24, p = 0.01), TRF increases (β = 20.68, 95% CI = 1.50, 39.86, p = 0.03), TOF increases (β = 57.92, 95% CI = -0.12, 115.95, p = 0.05), and BMC decreases (β = -6.84, 95% CI = -12.64, -1.04, p = 0.02).ConclusionsIn summary, our study demonstrated that a dose–response relationship exists between urinary nickel and body compositions, with a low inflection point level of urinary nickel for the saturation effect.

First-principles theory of the pressure-induced invar effect in FeNi alloys

Beside the classic Fe${}_{64}$Ni${}_{36}$ Invar alloy, which shows an anomalously low thermal expansion at ambient pressure, Fe-Ni alloys with a higher nickel composition can be driven to Invar behavior by pressure. The authors investigate the pressure induced Invar effect theoretically and demonstrate that it can be explained by a magnetic transition from a ferromagnetic state at high volume to a complex noncollinear state upon compression. They relate the Invar effect to the increasing contribution of magnetic entropy with pressure.

Investigation of 500 keV Si ion induced surface structuring of Ni and Ti for enhancement of field emission properties

The present paper reports the investigation of surface morphology, elemental composition, phase changes and field emission properties of Si ion irradiated nickel (Ni) and titanium (Ti). The Ni and Ti targets have been irradiated with 500 keV Si ions generated by Pelletron accelerator at various fluences ranging from 6.9 × 1013 to 77.1 × 1013 ions/cm2. Stopping range of ions in matter analysis revealed higher values of electronic stopping and sputtering yield for Ni as compared with Ti. For both irradiated metals, electronic energy loss dominant over the nuclear stopping. The growth of induced surface structures have been analysed by using field emission scanning electron microscopy (FESEM) analysis. In case of Ni, as the ion fluence increases from 6.9 × 1013 to 65.8 × 1013 ions/cm2, the formation of spherical particulates, agglomers and sputtering is observed. Although in the case of Ti, with the increase of Si ion fluence from 11.6 × 1013 to 77.1 × 1013 ions/cm2, the formation of irregular‐shaped particulates along with crater and sputtered channels is observed. X‐ray diffraction (XRD) analysis shows that no new phase is identified. However, a significant increase in peak intensity is observed with increasing ion fluence. The variation in crystallite size and dislocation line density is also observed as a function of Si ion fluence. Fourier transform infrared spectroscopy analysis shows that no bands are formed after the Si ion irradiation. Field emission properties of ion‐structured Ni and Ti are well correlated with the growth of surface structures observed by SEM and dislocation line density evaluated by XRD analysis.

Fractional Composition of Nickel, Manganese and Iron in Municipal Solid Waste Incineration Bottom Ash

Fractional Composition of Nickel, Manganese and Iron in Municipal Solid Waste Incineration Bottom Ash

High performance of non-enzymatic glucose biosensors based on the design of microstructure of Ni2P/Cu3P nanocomposites

The transition-metal phosphides with metalloid characterics, exhibiting great application potential in the field of glucose detection that plays an important role in the treatment of diabetes, can achieve high sensitivity as a eletrocatalyst for nonenzymatic glucose sensors. However, it has the drawbacks of low detection range and difficulty in manufacture. In this work, a hybrid heterogeneous nanocomposite of copper and nickel phosphide (Ni2P-Cu3P) has been designed and successfully prepared by a mild one-step solvothermal method. Inspired by the porous characteristic of sponges, the mesoporous structure with a much larger surface area has been constructed by adjusting the reaction conditions and the element composition of copper and nickel to have more active sites, thus broadening linear range. The precisely designed heterogeneous nanostructure and the unique mesoporous morphology of Ni2P-Cu3P were confirmed and characterized by the XRD and TEM analysis. Electrochemical oxidation of glucose on the composite modified glassy-carbon electrode (Ni2P-Cu3P/GCE) was measured by chronoamperometry and cyclic voltammetry. At the optimal test potential of + 0.64 V, the Ni2P-Cu3P/GCE hybrid electrode possessed an ultra-high sensitive response of 4700 μA mM−1 cm−2 to glucose, in a broad linear range from 4 μM to 5 mM, and a low detection limit of 0.1 μM at an S/N ratio of 3. The electrode also exhibits excellent anti-interference properties towards other common co-existing electroactive distractions, such as ascorbic acid, uric acid, urea, dopamine, etc.

Nickel and Chromium Stable Isotopic Composition of Ureilites: Implications for the Earth's Core Formation and Differentiation of the Ureilite Parent Body

AbstractWe report the first Ni and Cr stable isotope data for ureilite meteorites that are the mantle residue of a carbon‐rich differentiated planet. Ureilites have similar Ni stable isotope compositions as chondrites, suggesting that the core‐mantle differentiation of ureilite parent body (UPB) did not fractionate Ni isotopes. Since the size of Earth is potentially larger than that of UPB; with diameter &gt;690 km), resulting in higher temperatures at the core‐mantle boundary of Earth, it can be predicted that the terrestrial core formation may not directly cause Ni stable isotope fractionation. On the other hand, we also report high‐precision Cr stable isotope composition of ureilites, including one ureilitic trachyandesite (ALM‐A) that is enriched in lighter Cr stable isotopes relative to the main‐group ureilites, which suggests that the partial melting occurred on UPB. The globally heavy Cr in the UPB compared to chondrites can be caused by sulfur‐rich core formation processes.

Synthesis and characterization of nickel oxide nanoparticles using Clitoria ternatea flower extract: Photocatalytic dye degradation under sunlight and antibacterial activity applications

The present study is aimed to synthesize nickel oxide nanoparticles (NiO NPs) by using medicinal flower extract of Clitoria ternatea and examine its antibacterial and photocatalytic dye degradation activities. The synthesized NPs were investigated using UV–visible spectroscopy wherein they exhibited a color change pattern and confirmed their maximum absorption peak at 280 nm, which is distinct for NiO NPs. The FTIR analysis showed the presence of various functional groups in the flower extract as well as on the NiO NPs. XRD studies revealed the high crystalline nature of NiO NPs with 9.6 nm average size. The TEM micrograph shows hexagonal shape of the NPs that are non-agglomerated with a particle size of 13 nm. The composition of nickel and oxygen elements was confirmed through EDX studies. Using the well diffusion method, the antibacterial activity of NiO NPs was tested against both gram positive and gram-negative bacterial strains of Staphylococcus aureus and Escherichia coli. Additionally, photocatalytic degradation of Fast Green (FG) and Rose Bengal (RB) dye molecules were performed by using NiO NPs. Based on the obtained results, we confirmed that NiO NPs degrade FG by 89 % and RB by 77 % in the presence of sun light.