
CNT-added surface treatment (CAST) is a newly developed technology that incorporates single-walled carbon nanotubes (SWCNTs) into a metal surface through alternate current electrolysis using a dispersion of SWCNTs in an alkaline aqueous solution. We apply this method to Al-plates and characterize their surface morphology and components through scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. After CAST processing, protrusion structures of Al-oxide containing SWCNTs are formed on the surface of the Al-plate, and the surface morphology differs significantly from that of the surface of Al films treated through conventional anodic oxidation. The height and spacing of the protrusion structures formed on the surface of the CAST-treated Al-plates are 100 - 200 nm and 50 - 100 nm, respectively. In addition, we investigate the formation mechanism of the protrusion structure by applying a DC voltage between the working electrode (Al-plate) and a counter electrode immersed in a dispersion of SWCNTs in an alkaline aqueous solution. Comparing the Al-plate surface after treatment under both current directions, we propose a model for the formation process of protrusion structures containing SWCNTs based on catalyst surface etching.
The performance of many optical glass elements depends on the structure of the surface.The high refractive index of flint glass is advantageous in constructing some optical elements (lenses, prisms, beam splitters, …).Also, high achromaticity and size reduction in oblique incidence TIR (total internal reflection) phase retarders require high-index glass.The present work is interested in studying the optical properties of the thin surface layer formed on TIR rhomb retarder at different wavelengths to indicate the extent to which this surface layer affects the performance of this TIR rhomb retarder and show how to overcome this effect.
This study uses Steel Slag Coarse Aggregate (SSCA) as a mixture replacement, preamble material to improve soft soils, which is economic, and has good effect environment.Recently, the development and utilization of by-product, waste and recycle materials must be studied and investigated as a source of improved material for soft soils as, an economic and good effect environmental.The study analyzes effects of both replaced mixtures, (SSCA) or (TSCA) on improved soil bearing capacity and expected settlement after verifying the model.Numerical modeling of the one of real store loaded strip using, PLAXIS, 2D, strain deformation behavior to achieve field visible and measured deformations of untreated soft soil.Numerical studies were devolved to investigate geomechanics parameters improved to compare between using (SSCA) or (TSCA) as, replacement mixture.Results demonstrate that using (SSCA) improved compressibility and strength of shallow soft soil layer significantly than using (TCSA) mixture, while (SSCA) improved strip footing ultimate bearing capacity, (UBC), by 84.4% compared with increase of 20.5% when using (TCSA) mixture at the same thickness.In addition, the study highlights the effective (SSCA) replacement thickness ranges between (0.65 ~ 0.80) footing width.
Herein, we demonstrate a simple and inexpensive one-pot green synthesis of silver nanoparticles (Ag-NPs) functionalised with a combination of banana peel (Musa paradisiaca) and grape (Vitis vinifera) fruit extracts.The reaction mixture of aqueous silver nitrate, banana peel and grapefruit extracts revealed a dark brown colour after a reaction time of 18 minutes, which indicates the presence and the successful synthesis of silver nanoparticles.The optical and structural properties of the green synthesised nanoparticles were analysed using UV-Visible spectroscopy (UV-Vis) which confirmed an absorption band at 440 nm.The polydispersity nature and the AgNPs sizes of 30 nm were revealed using small angle X-ray scattering (SAXS) and high-resolution transmission electron microscopy (HR-TEM) techniques.Fourier transform infrared spectroscopy (FT-IR) studies revealed the structure of these nanoparticles which included carbonyl groups, primary amine groups, OH groups and other stabilizing functional groups characteristic of the properties of combined extracts.A simple, quick, less time-consuming surface plasmon resonance (SPR) and electrochemical method in the form of optical and electrochemical sensors have been developed for the detection of Escherichia coli 0157:H7.The obtained limit of detection (LOD) values for SPR and GBPE-Ag-NPs/GCE-based sensor systems were found to be 1 × 102 CFU/mL and 3.5 × 101 CFU/mL, respectively.The obtained values fall within the range for E. coli 0157:H7 in seawater.
This study reports on the novel and simple green method involving the use of apple (Malus domestica) and tomato (Solanum lycopersicum) extracts in the synthesis of electroactive layers of silver nanoparticles|graphene oxide (AgNPs|GO) and zinc oxide nanoparticles|graphene oxide (ZnONPs|GO).The surface morphology of the green synthesized nanocomposites was studied using High-Resolution Transmission Electron Microscopy (HRTEM), High-Resolution Scanning Electron Microscopy (HRSEM) while the elemental analysis was studied using Fourier Transform Infrared Spectroscopy (FTIR), Raman spectroscopy and X-Ray diffraction (XRD) and their optical properties were further characterised using Ultraviolet Spectroscopy (UV-vis).The electrochemical studies of these nanocomposites were achieved using cyclic voltammetry (CV) where an increase in electron conductivity of the AgNPs|GO and ZnONPs|GO nanocomposite was observed.Comparatively, the silver nanoparticulate-based platforms were observed to have superior electrochemical properties as opposed to the zinc oxide-based platform.The observed electrochemical activities of the synthesized nanocomposites are a good indication of their suitability as electroactive platforms towards the development of electrochemical sensors.Electrochemical sensors are popular in the Electrochemistry field because they may be developed using different methods in order to suit their intended analytes.As such, the synthesis of a variety of electrochemical platforms provides researchers with a vast range of options to select from for the detection of analytes.
The fundamental scientific problem for micro- and nano-electronics has been solved—methods for creating and investigating properties of physically doped materials with spatially inhomogeneous structure at the micro- and nano-meter scale have been developed. For the application of functional nanocomposite film coatings based on carbides of various transition metals structured by nanocarbon, for the first time in the world, we developed a new technique for their plasma deposition on a substrate without the use of reaction gases (hydrocarbons such as propane, acetylene, etc.). We have created nanostructured film materials, including those with increased strength and wear resistance, heterogeneous at the nanoscale, physically doped with nanostructures—quantum traps for free electrons. We learned how to simultaneously spray (in a plasma of a stationary magnetron discharge) carbides and graphite from a special mosaic target (carbide + carbon) made mechanically. As a result of such stationary sputtering of carbides and carbon, plasma nanostructured coatings were obtained from nanocarbides, metal nanocrystals and nanocarbon. Our design of such a target made it possible to intensively cool it in the magnetron body and spray its parts (carbide + carbon) simultaneously with a high power density of a constant plasma discharge—in the range of values from 40 W/cm2 to 125 W/cm2. Such sputtering with a change in the power or the initial relative surface areas of various parts of the mosaic target (carbon and carbide) made it possible to change the average density of carbide, metal and carbon in a nanostructured (nanocarbon and metal nanostructures) coating. The changed relative density of various components of the nanocomposite (nanostructures of carbide, metal, and carbon in the form of graphite) significantly affected the physical properties of the nanocomposite coating. The creating method of multiphase nanostructured composite coatings (based on carbides of transition metals) with high hardness of 30 GPa, a low coefficient of friction to dry 0.13 - 0.16, with high heat resistance up to 3000°C and thermal stability in the nanocrystalline state over 1200°C is developed. It is established that the presence of nanographite in the composite significantly improves the impact strength and extends the range of possible applications, compared with pure carbides. The solution to this problem will allow creating new nanostructured materials, investigating their various physical parameters with high accuracy, designing, manufacturing and operating devices with new technical and functional capabilities, including for the nuclear industry and rocket science.
Most reports on the fabrication of high-quality Gallium nitride (GaN) are typically based on physical techniques that require very expensive equipment. Therefore, the electrodeposition was adopted and examined to develop a simple and economical method for GaN synthesis. GaN films are synthesized on aluminum substrates that are heat-treated at various temperatures using a low-cost and low-temperature electrochemical deposition technique. The electrochemical behavior of source ions in aqueous solutions is examined by cyclic voltammetry (CV). In the solution at pH 1.5 containing 0.1M Ga(NO3)3, 2.5 M NH4NO3 and 0.6 M H3BO3, reduction of gallium and nitrate ions are observed in CV. The presence of hexagonal GaN and gallium oxide (Ga2O3) phases is detected for the films deposited on Al substrates at -3.5 mAcm-2 for 3 h. The energy dispersive X-ray and mapping results reveal that Ga, O, and N coexist in these films. Raman analysis shows hexagonal GaN formation on Al substrates. The changes in the morphology and preferred orientation of GaN were found, which was caused by the reactivity of aluminum surface and the aluminum oxide layer formed by the heat treatment.
In the construction of biosensors, enzymes function as mediators converting biological signals generated by specific biological processes, into electrochemical signals. The ideology of bio-sensor design is retention of electron transfer activity of the enzyme utilizing superior interfacial architecture. In this work a Schiff-base macromolecule has been synthesized by reflux of 2, 3-diaminonaphthalene and pyrrole-2-carboxaldehyde starting materials. The Schiff-base ligand was subsequently complexed with FeCl2?4H2O under reflux, to produce the Fe-Schiff-base complex. The Schiff-base ligand and Fe-Schiff-base complex were characterized using nuclear magnetic resonance (NMR) spectroscopy, Ultra Violet/Visible (UV/Vis) spectroscopy, Fourier transfer infrared resonance (FTIR) and electron energy loss spectroscopy (EELS) to confirm the structure of the synthesis products. NMR spectroscopy confirmed the imide linkage of Schiff-base formation as two symmetrical peaks at 8.1 and 7.7 ppm respectively. Comparison of starting materials and product spectra by UV/Vis spectroscopy confirmed the disappearance of the diaminonaphthalene peak at 250 nm as evidence of complete conversion to product. FTIR spectroscopy of the Schiff-base ligand confirmed the formation of the imine bond at 1595 cm-1. EELS spectra comparing FeCl2?4H2O and the Fe-Schiff-base complex, showed good agreement in the energy loss profiles associated with changes to the electronic arrangement of Fe d-orbitals. EDS clearly identified a spectral band for Fe (7 - 8 eV) in the Fe-Schiff-base complex. Electrochemical evaluation of the Fe-Schiff-base complex was compared to the electrochemical signature of denatured cytochrome-C using cyclic voltammetry and square wave voltammetry. The Fe2+/Fe3+ quasi-reversible behavior for iron in the metallated complex was observed at -0.430 V vs. Ag/AgCl, which is consistent with reference values for iron in macromolecular structures.
Titanium alloys are widely used in the aerospace industries because of their excellent strength-to-weight ratio, high resistance to corrosion, high chemical reactivity and low thermal conductivity and ability to withstand high temperatures. However, these properties make titanium alloys difficult to machine. Drilling of titanium alloy may generate high temperature and high cutting forces. This paper is aimed at determining the suitable cutting parameters in the drilling of titanium alloys to minimize the cutting temperature and cutting forces. A finite element 3D model of the drilling process is simulated in this research. A combination of drilling speeds and feed rates are simulated to obtain the resulting responses of cutting force and temperature. The central composite design (CCD) is used to generate different combinations of cutting parameters to reduce the number of experiments and optimize the temperature and cutting force responses. Results show at the drilling speed of 5000 rpm with a feed rate of 0.1 mm/rev, temperature and cutting force significantly reduced.
The synthesis of the thenoyltrifluoroacetone compound doped with terbium, dysprosium and europium encapsulated in a silica matrix (TTA:Tb:Dy:Eu@SiO2) were performed by the sol-gel method. The precursors to obtain the vitreous phase (SiO2) were: Tetraethylorthosilicate (TEOS, C8H2O4Si, 98%, Aldrich), and ethyl alcohol (CH3CH2OH, 99.5%, Meyer), distilled water and 0.05 ml of hydrochloric acid (HCl, Meyer). The sample with molar ratio 20:80 TTA:Tb:Dy:Eu@SiO2 has the best emission intensity. Thermogravimetric analysis (TGA) shown that silica encapsulated samples decompose at lower temperatures than pure TTA:Tb:Dy:Eu luminescent material. Fourier Transform Infrared (IR-TF) shown the characteristic Si-O-Si bands that are presented at a wavelength of 1049, 853 and 440 cmǃ confirming that the luminescent material is encapsulated in a silica matrix, finally X-ray diffraction (XRD) shown that TTA:Tb:Dy:Eu@SiO2 composite is amorphous.
Laser Chemical Machining (LCM) is a non-conventional processing method, which enables very accurate and precise ablation of metallic surfaces. Material ablation results from laser-induced thermal activation of heterogeneous chemical reactions between electrolytes and a metallic surface. However, when processing metallic surfaces with LCM, large fluctuations in ablation quality can occur due to rising bubbles. The for-mation of bubbles during laser chemical machining and their influence on the ablation quality has not been investigated. For a more detailed investigation of the bubbles, ablation experiments on Titanium and Ce-ramic under different thermal process conditions were performed. The experiments were recorded by a high-speed camera. The evaluation of the video sequences was performed using Matlab. The resulting bubbles were analyzed regarding their size and frequency. The results show that boil-ing bubbles formed on both materials during processing. Titanium also produces smaller bubbles, which can be identified as process bubbles ac-cording to their size. Furthermore, it was found that undisturbed laser chemical ablation can be achieved in the presence of a boiling process, since both boiling bubbles and process bubbles were detected during machining within the process window.
The paper describes the research of coatings on the AK9 aluminum alloy substrate and hybrid coatings deposited on graphite substrate. Coatings on the AK9 alloy were deposited by thermal spraying and PVD method (physical vapour deposition). Hybrid coatings consisting of a tungsten interlayer and an external layer of Zr + DLC (diamond-like carbon) and CVD were deposited on the graphite surface. Plasma methods—PVD and CVD—were used. The structure and composition of coatings were analyzed.
Snails’ protection is essential because this species is to maintain a balanced ecology of water sources. They occur in rivers as well as ponds and balance the pH level of water. But these sources of water are contaminated by effluents, pollutants, acid rain, particulates, biological wastes etc. They can change the pH of water. Water is absorber of carbon dioxide and it converts carbon dioxide into carbonic. Other above mentioned wastes also increase the concentration of H+ ions in water. They produce hostile environment for snails. The outer part of snails is made of CaCO3. It produces chemical reaction in acidic medium and corrosion reaction is accelerated, and thus deterioration starts on the surface of snails. This medium makes their survival become miserable. For this work, corrosion of the snails’ study in the pH values of water is 6.5 in H2CO3 environment. The corrosion rates of snails were calculated by gravimetric methods and potentiostat technique. Aloe Vera was used for corrosion protection in acidic medium. The surface adsorption phenomenon was studied by Langmuir isotherm. Aloe Vera formed thin surface film on the interface of snails which adhered with chemical bonding. It was confirmed by activation energy, heat of adsorption, free energy, enthalpy and entropy. The results of surface coverage area and inhibitors efficiency indicated that Aloe Vera developed a strong protective barrier in the acidic medium.
Stainless steel alloy SS-304 is widely used in many engineering applications primarily for its excellent corrosion resistance, ease of fabrication and aesthetic appeal. Many kitchen appliances are made from SS-304 alloy because of its durability, ease of cleaning and beautiful finish. However, over the years of continuous usage and cleaning by detergent bar and abrasive clothes the initial brightness and shine of the plates and dishes undergo considerable degradation. In this work, we report the results of a thorough investigation of the physico-chemical characteristics of the surface regions of both new and old SS-304 plates of known history of continuous usage to identify the key physical and chemical factors that are responsible for the loss of shine. Several analytical techniques viz. SEM/EDX, AFM, XPS, XRD, Reflectance FTIR, Profilometry and Reflectance spectrometry in the visible region have been used for experimental investigation of surface structure, morphology, roughness profile, chemical composition and appearance measurements of several steel samples. In addition, glossmeter has been used to measure the gloss of the samples at certain specific angles. It seems that surface roughness is one of the key physical parameters that play an important role in the reduction of brightness and shine. The other parameter is the presence of a thin surface film on the steel surface. In order to analyze the experimental data and to predict the shine and brightness phenomena quantitatively, we have used Fresnel’s theory to compute first the reflectance from each component of SS-304 alloy assuming it to be a smooth surface and then extended it to compute the reflectance of the alloy surface (SS-304). In order to interpret the reflectance from old and used plates, we have further used Beckmann’s theory of light scattering from random rough surface to analyze and predict the appearance aspects of the alloy surface quantitatively. Both the experimental and computed results show good agreement, thus validating the reflectance model used for computing the reflectance from SS-304 alloy surface and the appropriateness of Beckmann’s model of random rough surface.
The addition of superelastic NiTi to electroless Ni-P coating has been found to toughen the otherwise brittle coatings in static loading conditions, though its effect on erosion behaviour has not yet been explored. In the present study, spherical WC-Co erodent particles were used in single particle impact testing of Ni-P-nano-NiTi composite coatings on API X100 steel substrates at two average velocities—35 m/s and 52 m/s. Erosion tests were performed at impact angles of 30°, 45°, 60°, and 90°. The effect of NiTi concentration in the coating was also examined. Through examination of the impact craters and material response at various impact conditions, it was found that the presence of superelastic NiTi in the brittle Ni-P matrix hindered the propagation of cracks and provided a barrier to crack growth. The following toughening mechanisms were identified: crack bridging and deflection, micro-cracking, and transformation toughening.
The frictional resistance and machining quality when cutting carbon fiber reinforced plastics (CFRP) laminates are associated with tribological behavior of tool materials. In the present study, the tribological properties of three types of monolayer microcrystalline diamond (MCD) coatings, nanocrystalline diamond (NCD) coatings and dual-layer MCD/NCD coatings sliding against CFRP are investigated under dry lubricated conditions using the rotational friction tester. The coefficients of friction (COF), wear rate and worn surfaces of the contacted surfaces are analyzed for the MCD-CFRP, NCD-CFRP and MCD/NCD-CFRP contacting pairs. The results show that compared with the monolayer MCD and NCD, the bilayer of MCD/NCD coating displays the lowest COF with the value of ~0.13, it is 42% and 55% of the values for MCD and NCD coatings. Due to the rough surfaces of MCD, the wear debris of CFRP on MCD samples exhibits the plowing effect. While for the NCD and MCD/NCD samples, the wear fragments display the planar shapes. The wear rate of CFRP against MCD is more than twice that of CFRP against NCD, due to the excellent loading capacity. While the wear rate of CFRP against MCD/NCD is about twice than that of CFRP-NCD pairs. The bilayer of MCD/NCD combines the excellent advantages of high hardness of MCD and the smooth surface of NCD. It shows the broad application potential for the bilayer coatings.
Electrochemical impedance spectroscopy was employed to investigate the permeation of electrolyte ions in thioctic acid self-assembled monolayer when its structure was changed by the interaction of copper ions. The ion permeation was evaluated by using relatively low excitation frequencies, 0.2 Hz to 1000 Hz, and quantified by an extra resistive component in the equivalent circuit (RSAM). The extent of ion permeation affected by the electrode potentials and the electrolyte concentration were investigated. The experimental results verified that RSAM decreased ~70% by interaction with copper ions and that RSAM increased ~2 - 3 times when the electrolyte concentration was decreased by 10 times. This analysis can be performed without addition of redox species.