Extraction of Uranium(VI) and Thorium(IV) from Nitric Acid Solution by N,N,N′,N′ – Tetraoctylglutaricamide

Synthesis and characterization of N,N,N′,N′-tetraoctylglutaricamide (TOGA) was carried out and used for extraction of U(VI) and Th(IV) from nitric acid solutions. The processes of extraction were determined by the slope analysis and by analyzing a function that allows the simultaneous treatment of all the experimental points obtained in different conditions. The different factors affecting the extraction distribution ratio(D) of U(VI) and Th(IV) (extraction concentration, concentrations of nitric acid, salting-out agent NaNO₃ concentration, equilibration time, temperature, and types of diluents) were investigated. The results obtained indicated that the extraction species of U(VI) and Th(IV) are mainly extracted as UO₂(NO₃)₂·1.0TOGA and Th(NO₃)₄·1.5TOGA. The apparent equilibrium constant of U(VI) and Th(IV) extraction determined are 3.35 ± 0.03 L³/mol³ and 1.87 ± 0.01 L⁵/mol⁵ at 298 ± 1 K. Thermodynamic parameters such as the free energy(ΔG), enthalpy(ΔH), and entropy(ΔS) changes associated with the extraction processes could be evaluated. Back-extraction of U(VI) and Th(IV) from organic phases was also studied.     

The Vinylation of Aryl Iodides Catalyzed by Silica-Supported Poly-γ-aminopropylsilica Ni, Cu and Co Complexes

Silica-supported poly--aminopropylsilica Ni, Cu and Co complexes were prepared from poly--aminopropylsilane and fumed silica, followed by treatment with metal acetate in ethanol. These catalysts are highly active and stereoselective for vinylation of aryl iodides with olefins. They give a variety of trans-substituted products in high yields in both polar and non-polar solvents at 120-150 °C, and can be reused without loss in activity.     

Extraction of europium and electrodeposition of Al–Li–Eu alloy from Eu2O3 assisted by AlCl3 in LiCl–KCl melt

The work presents an electrochemical study on preparation of Al–Li–Eu alloys on a tungsten electrode in molten LiCl–KCl–AlCl₃–Eu₂O₃ system at 753 K and 953 K. Gibbs energy shows that AlCl₃ can chloridize Eu₂O₃, with a discharge in the form of Eu(III) ions on the cathode. The electrochemical behavior of Al(III), Li(I) and Eu(III) and alloy formation processes were investigated by cyclic voltammetry, square wave voltammetry, and chronopotentiometry. Cyclic voltammetry indicated that the underpotential deposition of europium on pre-deposited Al forms two Al–Eu intermetallic compounds at electrode potentials around ?2.00 V and ?2.34 V, respectively. And the underpotential deposition of lithium on Al surface at about ?2.24 V leads to a formation of Al–Li alloy. X-ray diffraction (XRD) indicated that Al–Li–Eu alloys with different phases were obtained via galvanostatic electrolysis. The microstructure and micro-zone chemical analysis of Al–Li–Eu alloy were characterized by scanning electron microscopy (SEM) with energy dispersive spectrometry (EDS), respectively. The analysis of EDS showed that element Eu mainly distributes on needle-like precipitate, and not homogeneously in the Al–Li–Eu alloy. Composition of the alloys was analyzed by inductive coupled plasma analysis, and current efficiency was also determined with respect to the alloy composition.     

Microstructure,phase, magnetic properties,and electromagnetic wave absorption of graphene oxide – Ni0.7Zn0.3Fe2O4 – Al2O3 aerogel

In this work, an ultralight nanocomposite of graphene oxide aerogels as a matrix and nickel-zinc ferrite (Ni_0.7Zn_0.3Fe₂O₄) nanoparticles as a second phase for the absorption of electromagnetic waves in the frequency of 1–18 GHz were fabricated by the hydrothermal - freeze-drying method. α-Al₂O₃ nanoparticles were used for further impedance matching for applications in electromagnetic wave absorption. XRD, SEM, EDS, and VNA analyses were used to characterize the sample. The effects of the amount of Ni_0.7Zn_0.3Fe₂O₄ (NZF) nanoparticles (GO: NZF volume percent ratio = 5:1 and 2:1) on the absorption of electromagnetic waves were investigated.     

Investigation of structural,magnetic and Mössbauer properties of Co2+ and Cu2+ substituted Ni–Zn nanoferrites

We investigated the effects of Co²⁺ and Cu²⁺ substitution on the super-exchange interactions in Ni–Zn nanoferrites. The cation distribution technique was taken into account to explain the results. To authenticate the cation distribution, we have estimated the cation distribution in the light of X-ray diffraction method, Mössbauer spectroscopic analysis, and magnetization study. Statistical model based on the cation distribution was used to calculate the Curie temperature. The values of magneton number n_B and Curie temperature T_C calculated by using the cation distribution is found to be in agreement with the experimentally obtained values.     

Nanostructured perovskite oxides – LaMO3 (M=Al,Co, Fe) prepared by co-precipitation method and their ethanol-sensing characteristics

Nanostructured La-based perovskite oxides − LaMO₃ (M=Al, Co, Fe) were synthesized by a new co-precipitation procedure using metal nitrate and carbonate salts as starting materials. X-ray diffraction and energy dispersive X-ray spectroscopic results confirmed the formation of single-phase nanocrystalline perovskite oxides with high purity. Characterizations by scanning/transmission electron microscopy and nitrogen adsorption revealed that LaAlO₃ was produced in the form of rectangular porous nanorods exhibiting much larger surface area and porosity compared with densely aggregated LaCoO₃ particles and loosely clustered LaFeO₃ nanoparticles with cracked-egg morphologies. The materials were characterized for gas sensing towards ethanol at 200–350 °C. From gas-sensing results, the LaAlO₃ sensor displayed n-type gas-sensing behaviors with considerably higher ethanol response than p-type LaFeO₃ and LaCoO₃ sensors, respectively. In particular, the LaAlO₃ sensor exhibited a high response of 16.45–1000 ppm ethanol and excellent ethanol selectivity against NO₂, SO₂, CO and H₂ at 350 °C. The superior gas-sensing performances could be attributed to the effective receptor function, transducer function and utility factor of LaAlO₃ nanorod structures prepared by the co-precipitation method.     

合成方法对NH_4MPO_4·H_2O(M=Mn,Fe,Co,Ni,Cu)颗粒形貌的影响

采用低温固相法与常规液相法合成系列磷酸铵复盐NH4MPO4.H2O(M=Mn,Fe,Co,Ni,Cu),用XRD,FT-IR和SEM对产物进行表征,比较两种合成工艺及产物的颗粒形貌和大小。结果表明,除铜盐为斜方晶系外,其余都为正交晶系。与常规液相法相比,低温固相法不需要使用溶剂,能在低温短时间内合成磷酸铵复盐类化合物,但是需要晶化才能得到良好结晶体,合成的条件较为苛刻,容易有副反应发生,所得产品是片状结构,厚度为纳米尺寸的二维纳米材料,液相反应得到的产物颗粒是层状结构的微米级产品。     

A comparative study of different concentrations of (Co/Ni/Cu) effects on elastic properties of Li–Mn ferrite employing IR spectroscopy and ultrasonic measurement

Three series of divalent ions (Co²⁺/Ni²⁺/Cu²⁺) substituted into lithium-manganese ferrites were synthesized using a typical ceramic technique. Two different methods were used to investigate their elastic properties. Infrared (IR) spectroscopy showed two essential bands referring to the tetrahedral ‘υ_A’ and the octahedral ‘υ_B’ sites. The force constant, elastic wave velocity and elastic moduli of all specimens have been calculated from the results of IR spectroscopy. Using the ultrasonic pulse transmission (UPT) technique, the longitudinal and shear wave velocities were measured. Using these values; bulk modulus (B), rigidity modulus (G), Young's modulus (E), and Poisson ratio (σ) were determined. In comparison, the elastic moduli resulting from IR spectroscopy results were larger than those obtained from UPT measurements. Because the present ferrite systems are porous, the elastic moduli of the compositions from UPT have been adjusted to zero porosity by two models. The values of the adjusted elastic moduli have been shown to have the same trend as those of the uncorrected elastic moduli. Elastic parameters have generally improved dramatically for Li–Mn–Co ferrite and Li–Mn–Ni ferrite compared to Li–Mn–Cu ferrite. Higher elastic moduli values have been obtained in Li–Mn–Co spinel ferrites, suggesting that such materials are ideal for use in core shapes. Two methods were used to evaluate the Debye temperature of all compositions.     

Adsorption of Cu(II) from Aqueous Solution by Porous Mn3[Co(CN)6]2 · nH2O Nanospheres

Prussian blue analogue of porous Mn₃[Co(CN)₆]₂ · nH₂O nanospheres with a large surface area were prepared by simple mixing K₃[Co(CN)₆]₂ and manganous nitrate solution at room temperature. The morphology and structure of the prepared products were characterized by XRD, FE-SEM, TEM, and BET. The results indicated that the product was composed of nanospheres with the diameter of ～250 nm, which was of porous structure with the pore diameter in the 2.5–4 nm range. The adsorption behavior of Cu(II) ions from aqueous solution onto porous nanospheres was investigated as a function of parameters, such as the equilibrium time, the pH, the initial concentration, and the temperature. A maximum adsorption capacity of 140.85 mg g^?1 of Cu(II) was achieved. Due to the simple synthetic method and its high adsorption capacity, the porous nanospheres had the potential to be utilized as an effective adsorbent for Cu(II) removal.     

Effect of the sintering temperature on microstructure and properties of Al2O3–Cu–Ni hybrid composites obtained by PPS

In the present research, the influence of sintering temperature on the microstructure and properties of Al₂O₃–Cu–Ni hybrid composites prepared by the Pulse Plasma Sintering (PPS) technique were described. In this research, three temperatures have been selected: 1250°C, 1300°C, and 1350°C. SEM observations were carried out to determine the distribution of the metallic phase in the composite depending on the sintering temperature. The conducted experiments and microscopic observations enabled a better understanding of the phenomena occurring between the ceramic matrix and metallic phase in the obtained materials. The mechanical properties like a hardness and fracture toughness were measured. The technology applied allowed us to obtain ceramic-metal composites with a homogeneous microstructure. It was found that the sintering temperature influences the selected physical and mechanical properties of the composites produced. It was found that samples produced at 1300°C are characterized by the highest relative density and the mechanical properties.     

Preparation of magnetically separable Cu6/7Co1/7Fe2O4–graphene catalyst and its application in selective reduction of nitroarenes

A magnetically separable and highly active Co–Cu mixed spinel catalyst, Cu_6/7Co_1/7Fe₂O₄–graphene (Cu_6/7Co_1/7Fe₂O₄–G), was fabricated by a hydrothermal method. The results demonstrated that the Cu_6/7Co_1/7Fe₂O₄–G possessed excellent catalytic activity for the reduction of a broad range of nitroarenes in the presence of NaBH₄. The composite catalyst was efficient, stable, low-cost and could be easily recovered due to its magnetic separability.     

Structural and mechanical properties of La0.6Sr0.4M0.1Fe0.9O3-δ (M: Co,Ni and Cu) perovskites

La_0.6Sr_0.4M_0.1Fe_0.9O_3-δ (M: Co, Ni and Cu) perovskite nanostructures were synthesized using low frequency ultrasound assisted synthesis technique and effect of substitution of Fe by Co, Ni and Cu on crystal structure and mechanical properties in La_0.6Sr_0.4FeO_3-δ perovskite was studied. The HRTEM and Rietveld refinement analyses revealed the uniform equi-axial shape of the obtained nanostructures with the existence of La_0.6Sr_0.4M_0.1Fe_0.9O_3−δ with mixed rhombohedral and orthorhombic structures. Substitution by Cu decreases the melting point of La_0.6Sr_0.4FeO_3-δ. The results of mechanical characterizations show that La_0.6Sr_0.4Co_0.1Fe_0.9O_3−δ and La_0.6Sr_0.4Ni_0.1Fe_0.9O_3−δ have ferroelastic behavior and comparable elastic moduli, however, substitution by Ni shows higher hardness and lower fracture toughness than Co in B-site doping.     

Structural analysis and characterization of doped spinel Co2−xMxTiO4 (M=Mg2+, Mn2+, Ni2+, Cu2+ and Zn2+) coated mica composite pigments

A new kind of composite mica pigments were prepared by coating Co_2−xM_xTiO₄ composite oxide nanoparticles onto mica, to investigate the effects of doping ions Mg²⁺, Mn²⁺, Ni²⁺, Cu²⁺ and Zn²⁺ on the properties of the doped composite pearlescent pigments, such as the crystal structure, color and shading power. The structure, morphology, color and shading power of the coated pigments were characterized by the X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis spectrophotometer and CIE L*a*b* methods. SEM images of coated pigments showed that mica were coated uniformly with a single layer of dispersed nanoparticles. Research of the doped composite pigments showed that the doping ions had entered into the spinel crystal structure, forming a new kind of composite mica pearlescent pigments coated with Co_2−xM_xTiO₄. For the analysis of color and shading power of the pigments, doping of Ni²⁺ and Zn²⁺ can improve the color and shading power of the doped pigments, but the larger dosage of Zn²⁺ doping can weaken the color and shading power of the doped pigments. Doping of Mg²⁺, Mn²⁺ and Cu²⁺ metal ions can also weaken the color and shading power of the doped pigments.     

Hierarchical Layered Porous SiO2 Supported Bimetallic NiM/EXVTM-SiO2 (M = Co,Cu, Fe) Catalysts Derived from Vermiculite for CO2 Reforming of Methane

Catalysis Letters - In this study, the two-dimensional layered porous silica material (EXVTM-SiO2) was designed and prepared by “expansion-acidification” modified vermiculite. Herein,...     

Hydrogenation of Sunflower Oil over M/SiO2 and M/Al2O3 (M = Ni,Pd, Pt,Co, Cu) Catalysts

This work is aimed at evaluating the performance of several catalysts in the partial hydrogenation of sunflower oil. The catalysts are composed of noble (Pd and Pt) and base metals (Ni, Co and Cu), supported on both silica and alumina. The following order can be proposed for the effect of the metal on the hydrogenation activity: Pd > Pt > Ni > Co > Cu. At a target iodine value of 70 (a typical value for oleomargarine), the production of trans isomers is minimum for supported nickel catalysts (25.7–32.4 %, depending on the operating conditions). Regarding the effect of the support, Al₂O₃ allows for more active catalysts based on noble metals (Pd and Pt) and Co, the effect being much more pronounced for Pt. Binary mixtures of catalysts have been studied, in order to strike a balance between catalyst activity and product distribution. The results evidence that Pd/Al₂O₃–Co/SiO₂ mixture has a good balance between activity and selectivity, and leads to a very low production of trans isomers (11.8 %) and a moderate amount of saturated stearic acid (13.5 %). Consequently, the utilization of cobalt‐based catalysts (or the addition of cobalt to other metallic catalysts) could be considered a promising alternative for the hydrogenation of edible oil.     

Preparation and Characterization of α-(Fe, Al)2O3 Solid Solutions by Sol–Gel Method

The aim of this paper is to synthesize α-(Fe, Al)₂O₃ solid solutions from precursors prepared by the sol–gel method. The powders were characterized by X-ray diffraction, particle size analysis and TGA-DSC. The results indicated that the precursor prepared by sol–gel method will translate into α-(Fe, Al)₂O₃ solid solutions after calcined at 1300 °C for 3 h, with the average grain size of 14 μm. And Fe₂O₃ reduced the temperature of the γ-Al₂O to α-Al₂O₃ phase transition from 1,300 to 850 °C.     

Effect of mechanical milling on structural,dielectric and magnetic properties of BaTiO3–Ni0.5Co0.5Fe2O4 multiferroic nanocomposites

The coexistence of ferroelectricity and ferromagnetism has triggered great interest in multiferroic materials. Multiferroic with strong room temperature magnetoelectric (ME) coupling can provide a platform for future technologies. In this paper, we have investigated the effect of mechanical milling on the properties of multiferroic nanocomposites synthesized by mixing barium titanate (BaTiO₃) (BT) and nickel cobalt ferrite (Ni_0.5Co_0.5Fe₂O₄) (NCF). This process has resulted into reliable disposal of a given quantity of NCF nanoparticles in BT grid and composite samples of different particle sizes (<500 nm) have been obtained by varying the duration of ball-milling for 12, 24, and 48 h. The presence of NCF within BT powder has been confirmed by X-ray Diffraction (XRD) and magnetization measurements (MH). Structural analysis was performed by using Reitveld refinement method that shows that the tetragonality of BaTiO₃ structure get reduced in submicron range. Variations in ferroelectric and dielectric properties with reduction in particle size/milling duration have been studied by P-E loop tracer and Impedance analyzer. The dielectric constant value of 400 has been observed for BT-NCF0 that increases to 9.7 K for composite sample ball mill at 48 h whereas remnant polarization increases to 4.2 μC/cm². These composites with high dielectric constant that changes with temperature and particles size find application in energy storage devices, sensor and memory devices.     

Study of structural,dielectric, electric,magnetic and magnetoelectric properties of K0.5Na0.5NbO3 − Ni0.2Co0.8Fe2O4 composites

Magnetoelectric composites with general formula (x) Ni_0.2Co_0.8Fe₂O₄- (1- x) (K_0.5Na_0.5)NbO₃ (x = 0, 0.10, 0.20, 0.30, 0.40, 0.50 and 1.0) have been synthesized by solid state reaction method. X-ray diffraction pattern asserts the existence of both the constituent phases in the synthesized composites. FESEM micrographs are used to investigate the microstructure and for calculation of average grain size of the composites. Temperature dependent dielectric properties are investigated as a function of temperature and found to enhance with addition of ferrite in the composites. P-E hysteresis loops obtained for individual (K_0.5Na_0.5)NbO₃ (KNN) phase and composites indicate the ferroelectric ordering in the composites. Saturation and remnant magnetization show increasing trend with increase in NCFO concentration. FC-ZFC magnetization curves indicate charge ordering, metal-insulator transition (Verwey transition) in NCFO and composites. Impedance spectroscopy shows that bulk resistance reduces with increase in temperature, thereby indicating negative temperature coefficient of resistance (NTCR) behaviour of the composites. The magnetoelectric effect is confirmed by measuring magnetoelectric voltage coefficient, α_ME and the maximum value of α_ME is 5.389 mV/cm-Oe for 20% NCFO-80% KNN composite.     

Determination of Cd,Cu, and Pb after Cloud Point Extraction using Multielemental Sequential Determination by Thermospray Flame Furnace Atomic Absorption Spectrometry (TS‐FF‐AAS)

Abstract

In the present paper a procedure for simultaneous preconcentration of Cd, Cu, and Pb using cloud point extraction (CPE) and multielemental sequential determination by thermospray flame furnace atomic absorption spectrometry (TS‐FF‐AAS) is proposed. This preconcentration procedure is based on the metals extraction into micellar media of octylphenoxypolythoxyethanol (Triton X‐114) after their reaction with 1‐(2‐pyridylazo)‐2‐naphtol (PAN). A Box‐Behnken design was used to optimize the variables (pH, buffer concentration and volume of NaCl) involved in the extraction procedure. Enrichment factors were calculated as the ratio between the slopes of calibration equations with and without the preconcentration procedure in the TS‐FF‐AAS, with values of 59, 25, and 21 respectively for Cd, Cu, and Pb. Limits of detection (LOD) (3s_b, n=10) were also calculated as 0.025, 0.38, and 0.43 µg L^?1 to Cd, Cu, and Pb, respectively. The precision (repeatability) expressed as relative standard deviation (RSD, n=10) for reference standards of 10.0 and 20.0 µg L^?1 were 6.1 and 4.5% for Cd, 7.2 and 3.4% for Cu and 5.2 and 8.7% for Pb. The accuracy was confirmed through the analysis of certified reference material (NIST 1643d, Trace elements in water). The developed procedure was also applied to Cd, Cu, and Pb determinations in mineral water samples.