


Том 53, № 6 (2017)
- Год: 2017
- Статей: 12
- URL: https://bakhtiniada.ru/1068-3755/issue/view/14265
Article
Influence of triazole stabilizers on the surface morphology of environmentally benign electroless nano copper deposition
Аннотация
In this work, we report the effect of triazole stabilizers: aminotriazole (ATA), benzotriazole (BTA), and tolytriazole (TTA) on the electroless deposition of copper thin film using xylitol containing copper methanesulphonate bath. Eco-friendly glyoxylic acid was used as reducing agent instead of p-formaldehyde which is carcinogenic. Potassium hydroxide was used for adjusting the pH, since it has the advantage of preventing the formation of insoluble byproducts in electroless bath, which is possible when NaOH is used. The electroless bath was optimized by addition of 1 ppm concentration of stabilizers, at 45°C and pH of 13.25 ± 0.25. Surface roughness, crystallite size and specific surface area of copper deposits were studied by the atomic force microscopy and X-ray diffraction. The anodic peak potential and corrosion current values were analyzed by the cyclic voltammetry and the Tafel plot. ATA was found to inhibit copper deposition while both BTA and TTA accelerated it. The crystallite size and surface roughness values were found to be less than 100 nanometer (nm) compare to the xylitol plain bath. TTA resulted in a better surface, structural, physical and electrochemical property of copper deposition than ATA and BTA.



Effect of vanadium doping on electrochemical properties of carbon coated nano lithium iron phosphate for high rate applications
Аннотация
Lithium iron phosphate (LiFePO4) is a promising electrode material for the lithium ion battery technology as it has the potential to meet the requirements of the high energy density and power density applications. However, its limitations such as low conductivity and a low diffusion coefficient lead to high impedance due to which its application is restricted. The cationic substitution of vanadium in the native LiFePO4/C is one of the methods to enhance the conductivity. Here the work is focused on obtaining a cathode material with improved electrical performance by doping it with different compositions of vanadium in the lithium site of LiFePO4/C. Nano powders of LiFePO4/C and Li1–xVxFePO4/C (x = 0.05, 0.1, 0.15–0.2) were synthesized from precursors via the solid state vacuum synthesis. The solid solution formation up to Li1–xVxFePO4/C (x = 0.2) without impurity phases is confirmed by the XRD and FTIR results. The particles distribution of synthesized powders was followed by the SEM. Also, dc conductivities are measured on sintered pellets and activation energies are calculated using the Arrhenius equation. The dependence of conductivity and activation energy of LiFePO4/C on variation of vanadium doping is also investigated in this study. The CR2032 cells were fabricated and subjected to cyclic voltammetry studies, charge-discharges at different C-rates and cycle life. The electrochemical impedance spectroscopy was used to obtain the ac impedance and diffusion coefficients, and the effect of doping on these parameters is discussed. It was observed that the room temperature dc conductivity was improved by vanadium doping when compared to LiFePO4/C (2.141 × 10–2 S cm–1) and it was maximum for Li0.85V0.15FePO4/C (22.201 × 10–2 S cm–1). It was also observed that the diffusion coefficient of Li+ in Li0.85V0.15FePO4/C (12.89 × 10–9 cm2 s–1) improved by two orders of magnitude as compared to that of pure LiFePO4 (10–12 cm2 s–1) and carbon coated nano LiFePO4/C (0.626 × 10–11 cm2 s–1). Cells with Li0.85V0.15FePO4/C are able to deliver useful capacity of around 101 mAh g–1 at 10C rate. More than 1000 cycles were achieved with Li0.85V0.15FePO4/C at 20C rate.



Methods for controlling the composition and morphology of electrodeposited Fe–Mo and Fe–Co–Mo coatings
Аннотация
The effect of the electrolyte composition and the stationary electrolysis parameters on the composition and morphology of Fe–Mo and Fe–Co–Mo coatings deposited from complex citrate electrolytes based on Fe(III) is studied. It is shown that, at a constant component ratio of с(Fe3+): с(Co2+): с(MoO2−4): с(Cit3–) = 2: 2: 1: 4, an increase in the electrolyte concentration leads to a decrease in the pH of the solution in a range of 4.85–4.30 and in the molybdenum content in the coating. An increase in the current density contributes to the molybdenum enrichment of the electrodeposited alloy in the entire range of electrolyte concentrations. The Fe–Mo alloy coatings have a rough microporous surface; an increase in the current density does not lead to significant changes in the surface topography. It is found that the formation of ternary coatings is characterized by the competitive reduction of iron and cobalt in the alloy; the molybdenum content depends on the current density. At a metal ratio of 3: 2: 1 and a molybdenum content of up to 17 at % in the Fe–Co–Mo alloy, the surface has a fine-grained needlelike structure typical of cobalt. With an increase in ic, the atomic fraction of molybdenum increases, while the surface becomes microglobular. The Fe–Co–Mo electrodeposits with a metal ratio of 2.5: 1.5: 1.0 and a molybdenum content of 19–20 at % have a more developed surface with a high density of spheroids.



Transport properties of solid solutions of хKYF4–(1–х)PbF2 system
Аннотация
In the system (1–x)PbF2–xYF3–xKF, solid solutions of aliovalent substitution with fluorite structure at 0.47 < x < 0.69 are formed, in which the fluorine ions are found to be in three structurally nonequivalent positions that differ in the local environment and mobility. There are immobile, locally mobile, and highly mobile anions. The conductivity of the synthesized polycrystalline samples is ensured by highly mobile interstitial fluoride ions, whose concentration and hence electrical conductivity increase on heating. The contribution of the surface conductivity of crystallites is not detected. The electronic component is two orders of magnitude lower than the ionic one.



Voltammetric responses of black radish enzyme preparation immobilized on kaolin and aerosil
Аннотация
The purpose of the paper was searching for new “green” energy sources. The changes in the mechanism and the selectivity of components binding from the enzyme mixture extracted from black radish adsorbed on kaolin and aerosil are demonstrated. The differences in the binding mechanisms of metal-containing sites of enzyme molecules based on the implementation of the spatial separation of enzyme fragments containing Fe, Ni, Cu and Zn-ions are mentioned. The implementation of the charge division forms of heterostructures improves the oxidation activity and stability of the immobilized enzyme mixture and creates conditions for the formation of regions capable for specific adsorption of a charge. The spatially separated binding of enzyme fragments to an inorganic carrier exhibits the stabilizing effect on the formation of the areas capable for charging and accumulating red-ox transformations. Electrochemical methods have shown a possibility for the formation of structures responsible for the accumulation of energy, like a supercapacitor, in the immobilized systems consisting of graphene covered by a natural enzyme bound to an inorganic carrier.



Electrochemical and adsorption studies for the corrosion control of 6061 Al alloy using eco-friendly inhibitor
Аннотация
Environmentally benign biopolymer dextran was used to control the corrosion of 6061 Al alloy in 1 M HCl. The electrochemical techniques employed for the studies were potentiodynamic polarization and electrochemical impedance spectroscopy. The surface morphology was studied by scanning electron microscopy and elemental mapping was done by the energy dispersive X-ray analysis. Dextran emerged as a potential green corrosion inhibitor for the corrosion control of 6061 Al alloy in an acidic medium. It acted as mixed inhibitor, underwent physisorption and followed the Langmuir adsorption isotherm.



Root and shoot extracts of Ajuga chamaecistus subsp. scoparia as natural inhibitors for 304 stainless steel corrosion in strong acidic medium
Аннотация
The inhibitive action of root and shoot extracts of Ajuga chamaecistus subsp. scoparia as a green inhibitors on corrosion of 304 stainless steel in the 6.0 M HCl solution was studied by the weight loss method, potentiodynamic polarization, electrochemical impedance spectroscopy, scanning electron microscopy, and atomic force microscopy. The results demonstrate that the extracts act as a show mixed-type inhibitor. The Nyquist plots display an increase of the charge transfer resistance with an increase of the inhibitor concentration and a decrease of the double layer capacitance. The effect of temperature and related activation parameters was deliberate. Adsorption of the extract followed the Langmuir isotherm model. The inhibition efficiencies found from electrochemical tests were in good agreement with those observed via the weight loss method. The inhibition efficiencies for root and shoot extracts are 99.4 and 99.6%, respectively.



Impact of supporting electrolytes on the stability of TiO2–Ti counter electrode during H2O2 electrogeneration
Аннотация
This work focuses on the role of common supporting electrolytes (SEs) in the electro-chemical inertness of Ti-based materials employed for the anodic (direct) oxidation coupled with H2O2 electro-generation at the graphite cathode for the concurrent decomposition of organic contaminants. SEs are added to boost up the ionic conductivity of solution but a question always remains on the effect of SEs on the stability of anode materials. The use of ClO4− is encouraged in the electro-Fenton process as it does not form complexes with Fe2+/Fe3+; however, it is found that ClO4− corroded the TiO2 coated Ti (TiO2–Ti) anode very fast (>60 min) and, Ti4+ ions formed a yellow color complex (λmax = 380 nm) with H2O2. The influence of Cl–, NO3− and SO 42− was insignificant on the stability of TiO2–Ti. The cell current efficiency of H2O2 formation dropped sharply with in the case of TiO2–Ti anode. The TiO2–Ti corrosion also reduced the mass transfer co-efficient of DO transport from bulk to the cathode surface because of Ti4+ adsorption on graphite.



Wear and corrosion studies of Fe–B–Cr alloy coating on en 24 steel by HVOF thermal spray method
Аннотация
This work investigate the wear behavior of Fe–B–Cr coatings on medium carbon steel (EN24) substrate is used for several automotive parts. The high velocity oxy-fuel (HVOF) method was used to create the new crystalline coating of Fe–B–Cr (composition of 59%Fe–26%B–15%Cr in wt %) on a medium carbon steel substrate (AISI 4340). The characteristics of powder and coating are investigated using scanning electron microscopy (SEM) merged with energy dispersive spectroscopy (EDS), optical microscopy (OM) and thermogravmentric analysis (TGA) which were undertaken in the partial characterization of the coating. The phase contents of both powder and coatings were studied by X-ray diffraction (XRD). The coatings consist of melted and un-melted particles identified in the coatings. Moreover, oxides and micro-cracks were observed at the surface. The mechanical property of the coatings was characterized using a microhardness test. The hardness value increased three times more than the substrate. The coated surface showed lower levels of porosity. Moreover, the electrochemical investigation found Fe–B–Cr coating on medium carbon steel. The corrosion test was carried out in an environment with 0.5 M of NaCl, which showed that the corrosion resistance improved by coating.



Corrosion inhibition behaviour of thiourea derivatives in acid media against mild steel deterioration: An overview
Аннотация
This paper summarizes the inhibitor activity of various reported thiourea derivatives in acid media used against the deterioration of mild steel. Acid solutions have been extensively employed in manufacturing and many industrial processes for pickling and removal of undesirable scale. Mild steel is highly susceptible to corrosion in such aggressive acid media. The additives such as inhibitors are widely employed in those cases to reduce the extent of corrosion as much as possible. The survey of literature on organic inhibitors clearly indicates the potential usage of thiourea derivatives as inhibitors of mild steel corrosion. The influence of physical-chemical properties on the inhibition activity of thiourea derivatives has been discussed. This information is highly useful for different industrial applications where good performing inhibitors are being required for protecting mild steel from aggressive acid media.






Elimination of irreversible effects during first charging of lithium battery anodes
Аннотация
The irreversible capacity of negative electrode in a lithium-ion cell is a widely described the phenomenon. Irreversible capacity losses are connected with formation of a solid electrolyte interface layer. This layer is growing on the electrode-electrolyte interface during first several charging cycles. The layer is indispensable for proper functioning of a lithium-ion cell. However, during this layer formation, the atoms of lithium are consumed in a range from 18 to 45% of the total amount of lithium atoms presented in cell. Demonstration of possibilities to suppress this phenomenon that occurs on a negative electrode interface is the main aim of this paper.


