Effect of zinc concentration on the magnetic properties of cobalt–zinc nanoferrite

Nano-cobalt–zinc ferrite (CZFO) Co_(1?x)Zn_xFe₂O₄ with varied quantities of zinc (x = 0.0, 0.1, 0.2, 0.3, 0.4) have been prepared by solution combustion method. X-ray diffraction and transmission electron microscopy confirmed the size, structure and morphology of the nanoferrites. The addition of zinc in cobalt ferrite has been shown to play a crucial role in enhancing the magnetic properties. Ferromagnetic ordering is observed in nano samples at room temperature. Zn substitution shows maximum saturation magnetization for x = 0.1, that is 56.74 emu/g and then decreases for further increase in Zn substitution. The dependence of Mössbauer parameters viz. isomer shift and hyperfine magnetic field with zinc concentration has been studied. Mössbauer results are also supported by magnetization data. The results obtained from this method make these samples suitable for preparing high quality nanocrystalline ferrite for high density data storage applications.     

Deposition of zinc–zinc phosphate composite coatings on steel by cathodic electrochemical treatment

The present work aims at the development of an energy-efficient and eco-friendly approach for the deposition of zinc phosphate coatings on steel. The study describes the possibility of preparing zinc–zinc phosphate composite coatings by cathodic electrochemical treatment using dilute phosphoric acid as an electrolyte and zinc as an anode. The methodology enables the preparation of coatings with different proportions of zinc and zinc phosphate by suitably varying the applied current density, pH, and treatment time. Adhesion of the coating on mild steel and adhesion of paint film on the phosphate coating were found to be good. The surface morphology of the coatings exhibited platelet-type features and small white crystals (agglomerated at some places) which represented zinc and zinc phosphate, respectively. An increase in current density (from 20 to 50 mA/cm²) increased the size of the zinc crystals, and coatings prepared at 40 and 50 mA/cm² resembled that of electrodeposited zinc. Since the proportions of zinc and zinc phosphate could be varied with applied current density, pH, and treatment time, it would be possible to use this methodology to prepare coatings that would offer different degrees of corrosion protection.     

Effect of dispersant agents on morphology and optical–electrical properties of nano indium tin oxide ink-jet ink

In this study, the effect of dispersant agents on rheology, surface tension, dynamic light scattering and morphology of two nano-ITO inks were investigated. The inks were formulated using two different dispersant agents and the rest of constituents remained unchanged. The inks were printed onto a glass substrate using an ink-jet printer. The printing task was set to one, three and five runs, in order to evaluate variations in optical and electrical properties, by changing the thickness of the printed film. Following initial drying of the printed pattern on to the substrate, the samples were subsequently heat-treated at different temperatures (350 °C, 450 °C, 550 °C) to assess the effect, if any, of heat-treatment temperature on morphology, optical and electrical properties of the treated ITO films. It was concluded that the type of dispersant, heat-treatment parameters and number of printing runs had a substantial effect on the electrical and optical properties of the ITO films.     

Effect of electrolyte concentration on morphology,microstructure and electrochemical impedance of anodic oxide film on titanium alloy Ti-10V–2Fe–3Al

Anodic oxide films were fabricated on titanium alloy Ti-10V–2Fe–3Al in ammonium tartrate solutions at the concentrations: 1, 3, 5, 10 and 15 g L⁻¹. The morphological characteristics and microstructures of the films of the alloy were studied by optical microscopy (OM) and Raman spectroscopy (Raman), respectively. The electrochemical impedances of the films in 0.5 mol L⁻¹ H₂SO₄ solution were investigated by electrochemical impedance spectroscopy (EIS). It was showed that different electrolyte concentrations led to different change rates of anodizing forming voltage. The change rate significantly affected the morphology, microstructure and electrochemical impedance of anodic oxide film. When electrolyte concentration was 5 g L⁻¹, anodic oxide film was the most uniform, exhibited by the least and smallest breakpoints on the film. In addition, the amount of crystal phase of the film was the largest at 5 g L⁻¹, showed by the highest intensity of Raman peaks. Furthermore, the electrochemical impedance of the film of the alloy was the greatest at 5 g L⁻¹, demonstrated by the highest values of polarization resistances and lowest values of capacitances. These phenomenon were associated with the minimum value of the change rate of anodizing forming voltage at 5 g L⁻¹.     

Effects of thiourea and urea on zinc–cobalt electrodeposition under continuous current

The effect of thiourea and urea on zinc-cobalt alloys obtained from chloride baths under continuous current deposition are described and discussed. The deposit morphology was analyzed using Scanning Electron Microscopy (SEM) and an X-Ray Diffraction (XRD) was used to determine the preferred crystallographic orientations of the deposits. The use of additives does not refine the grain size of the Zn–Co alloy and an especially porous alloy was produced in the presence of urea. The preferred crystallographic orientations of zinc–cobalt alloys do not change in the presence additives. Zinc–cobalt alloys were without texture in the presence and absence of additives. Also, in the absence of additive and in the presence of urea, the XRD lines of the Zn–Co alloys are slightly shifted with respect to the pure zinc XRD lines, whereas, in the presence of thiourea, the XRD lines are not shifted. The alloy composition was examined using Energy Dispersive X-ray Fluorescence Spectroscopy (EDXRF). The percentage of cobalt in the alloy decreases slightly from 1.04 to 0.91 wt.% in the presence of urea and in the presence of thiourea it increases from 1.04 to 7.70 wt.%. Voltammetric studies show that thiourea increases the reduction rate of cobalt. This explains the increase in cobalt percentage in the alloy in the presence of thiourea.     

Synthesis of lithium LiNi1−yCoyO2 from lithium carbonate,nickel oxide and cobalt carbonate and their electrochemical properties

LiNi_1?yCo_yO₂ (y = 0.1, 0.3 and 0.5) were synthesized by solid state reaction method at 800 °C and 850 °C from Li₂CO₃, NiO and CoCO₃ as starting materials. The electrochemical properties of the synthesized LiNi_1?yCo_yO₂ were investigated. As the content of Co decreases, particle size decreases rapidly and particle size gets more homogeneous. When the particle size is compared at the same composition, the particles synthesized at 850 °C are larger than those synthesized at 800 °C. Among LiNi_1?yCo_yO₂ (y = 0.1, 0.3 and 0.5) synthesized at 850 °C, LiNi_0.7Co_0.3O₂ has the largest intercalated and deintercalated Li quantity Δx at the first charge–discharge cycle, followed in order by LiNi_0.9Co_0.1O₂ and LiNi_0.5Co_0.5O₂. LiNi_0.7Co_0.3O₂ synthesized at 850 °C has the largest first discharge capacity (142 mAh/g), followed in order by LiNi_0.9Co_0.1O₂ synthesized at 850 °C (113 mAh/g), and LiNi_0.5Co_0.5O₂ synthesized at 800 °C (109 mAh/g).     

The influence of polyaniline (PANI) coating on corrosion behaviour of zinc–cobalt coated carbon steel electrode

Zinc–cobalt alloy plating (ZnCo) was successfully deposited on carbon steel (CS) applying current of 2 mA with galvanostatic technique. Polyaniline film (PANI) was synthesized with cyclic voltammetry technique from 0.20 M aniline containing 0.20 M sodium tartrate solution on zinc–cobalt plated carbon steel (CS/ZnCo) electrode. PANI film characterized by scanning electron microscopy (SEM), was covered with a dark green-brown homopolymer film of strongly adherent homogeneous characteristic while the other one was plated with a porous light ZnCo one. The corrosion behaviour of zinc–cobalt deposited carbon steel electrodes with and without polyaniline (PANI) film in 3.5% NaCl solution was investigated with AC impedance spectroscopy (EIS) technique and anodic polarization curves. The results showed that PANI coating led to decrease of the permeability of metallic plating. The PANI homopolymer film provided an effective barrier property on zinc–cobalt coating and a remarkable anodic protection to substrate for longer exposure time.     

Fretting wear and electrochemical corrosion of well-adhered CVD diamond films deposited on steel substrates with a WC–Co interlayer

Diamond films have been grown on carbon steel substrates by hot-filament chemical vapour deposition methods. A Co-containing tungsten-carbide (WC–Co) coating prepared by high velocity oxy-fuel spraying was used as an intermediate layer on the steel substrates to minimize the early formation of graphite (and thus growth of low quality diamond films) and to enhance the diamond film adhesion. The effects of the WC–Co interlayer on nucleation, quality, adhesion, tribological behaviour and electrochemical corrosion of the diamond film were investigated. The diamond films exhibit excellent adhesion under Rockwell indentation testing (1500 N load) and when subjected to high-speed, high-load, long-time reciprocating dry sliding ball-on-flat wear tests against a Si₃N₄ counterface in ambient air (500 rpm, 200 N, 300,000 cycles). A WC–Co interlayer with appropriate chemical pretreatment is shown to play an important role in improving the nucleation, quality and adhesion of the diamond film, relative to that shown by substrates without such pretreatment.     

Structure and thermal stability of zinc–nickel electrodeposits

ZnNi alloys were electrodeposited from a chloride bath on steel substrates. The effect of nickel bath concentration on chemical composition, structure and microstructure of the deposits is demonstrated. From 0 to 13 nickel, the phases obtained do not correspond to that reported on the thermodynamic phase diagram. It is shown that the substitution of zinc by nickel is responsible for the formation of distorted _d and _d phases corresponding to the supersaturated hexagonal phase of zinc and to the unsaturated cubic phase of Zn–Ni alloy, respectively. Differential scanning calorimetry indicates that the thermal instability of the alloys containing up to 13 wt of nickel, results from the crystallization of the phase from the _d and _d phases at around 200 °C and 250 °C, respectively.     

Role of defect states on nonlinear properties of 8 MeV electrons irradiated zinc oxide thin films under off-resonant regime

In the present work, ZnO thin films were synthesized by sol-gel with subsequent spin coating on corning glass substrates. To understand the variations in the structural, optical, and nonlinear optical properties of ZnO thin films, 8?MeV electron irradiation with different dose rates (0?kGy, 1?kGy, 5?kGy, and 10?kGy) was performed. The XRD spectra showed transition from polar crystal growth orientation to non-polar crystal growth orientation of the films when the irradiation dose rate was increased from 0?kGy to 10?kGy and this was attributed to the reduced thickness of the irradiated films. The generation of localized surface states below the conduction band upon electron irradiation was confirmed by the quantification of the Urbach energy. A large band gap shrinkage was observed in the irradiated films (3.31–3.10?eV) due to the enhanced surface states. The photoluminescence spectra showed reduction in the NBE emission due to the enhanced surface states in the irradiated films. Open aperture and closed aperture Z-scan measurements were performed to extract the nonlinear absorption coefficient (β) and nonlinear refractive index (n₂) values using 532?nm Nd:YAG laser having pulse width of 7?ns. The open aperture Z-scan profiles of the films showed the presence of normalized transmittance valley, which was attributed to the two photon absorption (TPA) behaviour. The reduction in the depth of the normalized transmittance valley in irradiated films was ascribed to the bleaching of carriers in the ground states due to their trapping in the defect states. The closed aperture Z-scan curves showed the presence of normalized pre-focal peak, followed by a valley, which is characteristic of the self-defocusing nonlinear refraction behaviour. The electron irradiation with different dose rates provided an opportunity to understand the variations in the optoelectronic properties of the ZnO thin films considering the various defect states generated upon irradiation.     

Synthesis,characterization and controlled release properties of zinc–aluminium-beta-naphthoxyacetate nanocomposite

An organic–inorganic nanohybrid nanocomposite was synthesized by co-precipitation method using beta-naphthoxyacetate (BNOA) as guest anion and zinc–aluminium layered double hydroxide (Zn–Al-LDH) as the inorganic host. A well-ordered nanohybrid nanocomposite was formed when the concentration of BNOA was 0.08 M and the molar ratio of Zn to Al, R = 2. Basal spacing of layered double hydroxide containing nitrate ions expanded from 8.9 to 19.5 Å in resulting of Zn–Al-BNOA nanocomposite was obtained indicates that beta-naphthoxyacetate was successfully intercalated into interlayer spaces of layered double hydroxide. It was also found out the BET surface area increased from 1.13 to 42.79 m² g^?1 for Zn–Al-LDH and Zn–Al-BNOA nanocomposite, respectively. The BJH average pore diameter of the synthesized nanocomposite is 199 Å which shows mesoporous-type of material. CHNS analysis shows the Zn–Al-BNOA nanocomposite material contains 36.2 % (w/w) of BNOA calculated based on the percentage of carbon in the sample. Release of BNOA from the lamella of Zn–Al-BNOA was controlled by the zeroth and first order kinetics at the beginning of the deintercalation process up to 200 min and controlled by pseudo-second order kinetics for the whole process. This study suggests that layered double hydroxide can be used as a carrier for organic acid herbicide controlled release formulation of BNOA.     

Effects of different chelating agents on the composition,morphology and electrochemical properties of LiV3O8 crystallites synthesized via sol–gel method

Lithium trivanadate (LiV₃O₈) crystallites have been synthesized via sol–gel processing using oxalic, tartaric, citric and malic acid as the chelating agents. The thermal decomposition process of the as-prepared LiV₃O₈ precursor was investigated by thermogravimetric (TG) and differential scanning calorimetry (DSC). The structure, morphology and electrochemical performance of the as-synthesized LiV₃O₈ samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and the galvanostatic charge–discharge test. Different chelating agents were introduced to investigate their effects on the products composition, morphology and electrochemical properties. Result show that the samples prepared with oxalic and tartaric acid are similar to show thin rod-like morphology in submicron size distribution while the samples prepared with citric and malic acid are found consisting of block-like crystallities in micron size. Further electrochemical results exhibit that the LiV₃O₈ particles with oxalic, tartaric, citric and malic acid exhibit an initial discharge capacity of 304.4 mA h/g, 296.8 mA h/g, 268.7 mA h/g and 275.3 mA h/g, respectively. After 20 cycles, they retain discharge capacity of 250.2 mA h/g, 237.6 mA h/g, 198.5 mA h/g and 206.8 mA h/g, respectively.     

Effects of hard-segment compositions on properties of polyurethane–nitrolignin films

Segmented polyurethane (PU) films from castor-oil-based PU prepolymer with different hard-segment compositions and nitrolignin (NL) were synthesized. Diisocyanates (DIs), such as 2,4-tolylene DI (TDI) and 4,4′-diphenylmethane DI (MDI), 1,4-butanediol (BDO) as a chain extender, and trimethanol propane (TMP) as a crosslinker were used to obtain PU films containing NL (UL) which were named as UL–TB for TDI and BDO, UL–TT for TDI and TMP, UL–MB for MDI and BDO, and UL–MT for MDI and TMP, respectively. The mechanical properties and thermal stability of the films were characterized by a tensile test and thermogravimetric analysis, respectively. The MDI-based UL films exhibited a higher tensile strength (σ_b) and thermal stability than TDI-based UL. However, the recoverability of the TDI-based UL films was better than that of others. The UL films with TMP (UL–TT and UL–MT) had higher σ_b and lower breaking elongation (ϵ_b) than the UL films with BDO (UL–TB and UL–MB), caused by enhancement in the crosslinking network of hard segments and microphase separation between soft and hard segments. The values of σ_b and ϵ_b of the UL films that contained NL were much higher than those of the PU films, which indicates that the introduction of NL increased the interaction between hard segments by crosslinking. The hydrogen bonding in the UL films was studied by infrared spectroscopy, which indicated that MDI favored the formation of hydrogen bonds, especially in the ordered domain. Differential scanning calorimetry, dynamic mechanical analysis, and wide-angle X-ray diffraction indicated that the UL films were compatible as a whole, but microphase separation existed between soft and hard segments and significantly affected the mechanical properties. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 3251–3259, 2001     

Processing influence on dielectric,mechanical, and electrical properties of reduced graphene oxide–TPU nanocomposites

Two different reduced graphene oxides (rGOs) with similar concentration of oxygen and defects and differences in exfoliation were prepared to produce the rGO/thermoplastic polyurethane nanocomposites by solution blending (SB) and melt compounding (MC). Morphology, electrical, and dielectric properties were studied. Large agglomerates have been observed for the composites produced by SB and discrete and low agglomerated rGO particles in the case on the composites produced by MC. These morphological differences justify the observations in hardness, electrical conductivity, and even in the dielectric properties. The composites do not follow Jonscher's universal power law (UPL) and a linear trend between UPL factors (Log A vs n) has been observed for composites produced by SB, however, no trend is observed in the composites produced by MC, being the first time observed. Differences in the tunneling effect and breakage of H-bonds within the polymer can be suggested from the dielectric relaxation characterization. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47220.     

Effect of particle morphology on viscoelastic and flexural properties of epoxy–alumina polymer nanocomposites

Nanocomposites were synthesised by dispersing two different types of alumina nanoparticles in epoxy matrix by ultrasonication. Alumina nanoparticles of two shapes, rod and spherical were selected to investigate the effect of particle morphology on viscoelastic and flexural properties of nanocomposites. Specific surface area of both the selected nanoparticles was kept in the similar range. Good dispersion of nanoparticles was observed through transmission electron microscopy. The addition of nanoparticles in epoxy had significant enhancement in the viscoelastic properties and moderate improvement in flexural properties of composites. Composites having alumina nanorods showed higher improvement both in storage modulus as well as in flexural properties in comparison to composites having spherical alumina nanoparticles. Efficacy of Mori-Tanaka method was explored in modelling storage modulus of nanocomposites. Assorted size of alumina nanorods based on particle size distribution was used to model composites with nanorods to see the effect of size assortment on storage modulus.     

Synthesis,characterization, and electrical properties of polypyrrole–bimetallic oxide composites

In this study, polypyrrole (PPy) and its bimetallic oxide composites (PPy–V₂O₅–MnO₂) were synthesized via a modified chemical oxidation polymerization method in the aqueous medium with FeCl₃·6H₂O as an oxidant. The synthesized materials were characterized with various analytical techniques to investigate their structural, crystallographic, thermal, morphological, optical, and electrical properties. The Fourier transform infrared study confirmed the successful synthesis of the materials, whereas the X-ray diffraction analyses showed the amorphous and crystalline natures of the PPy and PPy–V₂O₅–MnO₂ composites, respectively. The bimetallic oxide content improved the thermal stability of the composites, as ratified by thermal analysis. The synthesized PPy had a globular and spongy nature, whereas the composites were mixtures of short and long rod-shaped particles. The bimetallic oxide blend enhanced the doping, surface area and semiconducting nature of composites, and lower electrical resistance compared with those of the PPy. The resistance of the synthesized materials depended on the V₂O₅–MnO₂ blend content in the composites and the temperature. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 47680.     

Transparent semiconductor zinc oxide thin films deposited on glass substrates by sol–gel process

Transparent semiconductor ZnO thin films were spin-coated onto alkali-free glass substrates by a sol–gel process. The influence of ZnO sols synthesized via different solvents (2-ME, EtOH or IPA) on the surface morphologies, microstructures, optical properties and resistivities of the obtained films were investigated. The as-coated films were annealed in ambient air at 500 °C for 1 h. X-ray diffraction results showed all polycrystalline ZnO thin films to have preferred orientation along the (0 0 2) plane. The surface morphologies, optical transmittances and resistivity values of the sol–gel derived ZnO thin films depended on the solvent used. The ZnO thin films synthesized with IPA as the solvent exhibited the highest average transmittance 92.2%, an RMS roughness of 4.52 nm and a resistivity of 1.5 × 10⁵ Ω cm.