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Petroleum-based polymers pose significant environmental challenges; this prompts researchers to seek alternatives for the same. The foremost solution to replace petroleum-based packaging lies in bio-based polymers that can degrade with water, soil, and the environment. The most common and economical bio-based polymer today is polyvinyl alcohol (PVA), however, it has certain limitations such as brittleness, hydrophilic nature, etc. The primary objective of this study is to enhance the flexibility, transparency, barrier properties, and thermal stability of PVA by incorporating glycerol as a plasticizer. In this regard, thin films were prepared by utilizing a solution-casting technique (blade coating) upon the addition of numerous concentrations of glycerol ranging from 1 to 5 wt%. Here two sets of thin films were prepared i.e., with glycerol (modified) and without glycerol (pure PVA). Results suggest exceptional mechanical flexibility and enhanced optical properties in terms of improved transmittance (>90%) upon incorporation of glycerol into PVA. The modified films also demonstrated a significant increase in their water barrier capabilities in comparison to pure PVA films. When the concentration of glycerol reached to 5 wt%, a substantial increase in biodegradability and flexibility was witnessed resulting in reduced brittleness. Thus, the mechanical properties of the modified thin films exceeded that of pure PVA counterparts. The prepared thin films unveil exciting possibilities to be used in diverse applications; such as food packaging, membranes, biodegradable materials, etc,. The extensive discussion is presented in the light of observed results.

Green approaches for nanoparticle synthesis have emerged as biocompatible, economical, and environment-friendly alternatives to counteract the menace of microbial drug resistance. Recently, the utilization of honey as a green source to synthesize Fe2O3-NPs has been introduced, but its antibacterial activity against one of the opportunistic MDR pathogens, Klebsiella pneumoniae, has not been explored. Therefore, this study employed Apis mellifera honey as a reducing and capping agent for the synthesis of iron oxide nanoparticles (Fe2O3-NPs). Subsequent to the characterization of nanoparticles, their antibacterial, antioxidant, and anti-inflammatory properties were appraised. In UV-Vis spectroscopic analysis, the absorption band ascribed to the SPR peak was observed at 350 nm. XRD analysis confirmed the crystalline nature of Fe2O3-NPs, and the crystal size was deduced to be 36.2 nm. Elemental analysis by EDX validated the presence of iron coupled with oxygen in the nanoparticle composition. In ICP-MS, the highest concentration was of iron (87.15 ppm), followed by sodium (1.49 ppm) and other trace elements (2O3-NPs. Morphological properties of Fe2O3-NPs revealed by SEM demonstrated that their average size range was 100–150 nm with a non-uniform spherical shape. The antibacterial activity of Fe2O3-NPs was ascertained against 30 clinical isolates of Klebsiella pneumoniae, with the largest inhibition zone recorded being 10 mm. The MIC value for Fe2O3-NPs was 30 µg/mL. However, when mingled with three selected antibiotics, Fe2O3-NPs did not affect any antibacterial activity. Momentous antioxidant (IC50 = 22 µg/mL) and anti-inflammatory (IC50 = 70 µg/mL) activities of Fe2O3-NPs were discerned in comparison with the standard at various concentrations. Consequently, honey-mediated Fe2O3-NP synthesis may serve as a substitute for orthodox antimicrobial drugs and may be explored for prospective biomedical applications.

Concrete structural properties are compromised largely due to corrosion susceptibility of steel reinforcements. This results in weakening and eventual failure of structures. Several strategies have been employed in past to control corrosion and increase mechanical strength of concretes, in particular for structural applications. In this study, fly ash and polypropylene fibers were utilized as the admixtures for preparation of concrete blocks with variable water-cement (w/c) ratios i.e. 0.45, 0.5 and 0.65. Three different grades of cements were selected in this study namely OPC 43, OPC 53 and sulfate resistant one. Also, two different steel alloys were used i.e. ASTM-615 and ASTM-706, since both of them are very common reinforcement materials (rebars). The curing time of 56 consecutive days was employed before testing and characterization. The results suggest remarkable improvement in the mechanical properties of blocks upon the incorporation of admixtures. However, rebars exhibited highest corrosion rate in the presence of OPC 43 cement at w/c ratio of 0.65.

Wastewater treatment is indispensable as wastewater can lead to adverse health effects and deteriorate the quality of life on earth. Photocatalysis is a facile methodology to address this issue. In this study, nanocomposites (NCs) of manganese oxide (Mn3O4) and nickel oxide (NiO) were synthesized in different weight ratios via the solid-state reaction route. Structural properties, optical properties, surface morphology, and functional group analysis of the synthesized nanomaterials were conducted using X-ray diffraction (XRD), UV– Vis spectroscopy, scanning electron microscopy (SEM) along with energy-dispersive X-ray (EDX) analysis, and Fourier-transform infrared (FTIR) spectroscopy, respectively. The bandgap of the nanocomposite decreases significantly from 2.35 eV for the Mn3O4 NPs to 1.65 eV for the Mn3O4/NiO nanocomposite (NC). Moreover, adsorption studies followed by the photocatalytic performance of the Mn3O4/NiO NCs were evaluated to determine the removal of methylene blue (MB) dye from wastewater. The photocatalytic performance of the nanocomposite enhances as the ratio of Mn3O4 in the composite increases from one weight percentage to three weight percentage. The photocatalytic degradation efficiency was calculated to be 95%. The results show that the synthesized NCs could play an important role in photocatalytic wastewater purification and environmental remediation.

Titanium alloys, particularly Ti6Al4V, are commonly used in biomedical applications. However, the inclusion of aluminum (Al) and vanadium (V) in this alloy can cause cytotoxic effects in the human body, resulting in Alzheimer’s disease and cancer. This study compares the performance of biocompatible alloys containing non-toxic elements, such as tin (Sn) and niobium (Nb), which are considered safe for implantation. Two sets of alloys were selected, Ti5Sn and Ti5Sn5Nb, and their properties were compared to Ti6Al4V. First, the alloys were prepared using a power metallurgical technique. Then, their phase analysis, hardness, wear resistance, strength, and corrosion performance in simulated body fluid (SBF) solution were characterized. Optical microscopy was used to study the microstructure, XRD was used to identify phases, and electrochemical testing was conducted to assess the alloys’ anodic and cathodic characteristics. Nanoindentation techniques were used to analyze surface characteristics, such as elastic modulus, nano hardness, and wear resistance. The results showed the alloys containing Nb and Sn had lower corrosion rates in SBF solution compared to Al-containing alloys. Moreover, Nb-containing alloys exhibited the highest hardness, 72% higher than Al-containing alloys. The corrosion-resistant properties of the alloys containing Nb and Sn were higher than those without Nb or Sn, suggesting they may be ideal for orthopedic implants in humans.

The wide variety of uses for nanoparticles (NPs) is due to their unique combination of features in a single assembly. The arc melted copper-cobalt ingot sample were qualitatively studied using laser induced breakdown spectroscopy (LIBS). Later, using the fabricated alloy as a target material for Nd:YAG laser ablation, CuCo2O4 NPs were synthesized. The magnetic properties of the synthesized NPs were studied using a vibrating sample magnetometer (VSM). To determine the composition and morphology of the synthesized NPs, X-ray diffraction (XRD), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and dynamic light scattering (DLS) techniques were used. The TEM and DLS showed that particles were spherical in shape with an average size of 32 nm and 28 nm, respectively. The antibacterial activity of the synthesized NPs was studied against S. aureus and E. coli strains as positive and negative controls using a standard approach. CuCo2O4 nanoparticles exhibited non-mutagenic potential against S. typhimurium TA-98 and TA-100 strains. Furthermore, the magnetic hyperthermia study of CuCo2O4 nanofluid was examined using a lab-made apparatus. The specific absorption rates (SAR) of 4.57 and 5.17 W/g were determined for the magnetic field strength of 230 μT and 247 μT, respectively. The study shows antibacterial activity and magnetic hyperthermia potential of the synthesized nanoparticles.

This research is aimed at the up-gradation of indigenous Pakistani iron ore, i.e., Dilband iron ore (hematite), by utilizing common metallurgical processes. First, the magnetic properties of the ore were determined. Initially, the iron ore samples contained 34 wt. % Fe in addition to other gangue materials. Therefore, the ore was subjected to a high-temperature reduction roasting process between 800 °C and 1000 °C. Additionally, the magnetic separation process was also employed. The influence of different roasting parameters, such as the reduction time, coal-to-ore ratio, and temperature, was examined. This was followed by characterization techniques using XRD (X-ray diffraction analysis), the Rietveld method, wet chemistry analysis, and a VSM (Vibrating Sample Magnetometer). The results suggest an excellent reduction at 900 °C for a coal/ore ratio of 20 wt. %, which was achieved within 2 h of the process. The Fe concentration increased tremendously from 34 to 56 wt. %, and in conjunction, magnetic properties were also induced (1.5 emu). The recovery was found to be substantial for the ore when the Fe content was 75 wt. %. Additionally, the economic feasibility of the processed ore was also studied, followed by an extensive analysis of the roasting and magnetic separation processes.

Nickel-supported hierarchical zeolite catalysts were prepared through a desilication reassembly process under optimized conditions and applied in one-pot menthol synthesis. In this work, the hierarchical zeolite-supported metal bifunctional catalysts were prepared with the help of desilication re-assembly and wetness impregnation techniques and applied in menthol synthesis via citral hydrogenation. The prepared catalysts were characterized using PXRD, BET, FE-TEM, NH3-TPD, H2-TPR, pyridine adsorption, and ICP-OES techniques. As a result, the physicochemical and acidic properties, such as mesopore surface area, metal dispersion, acidity, catalytic activity, and strong Lewis acid sites of pure microporous ZSM-5/USY zeolites, were significantly improved. Consequently, with the occurrence of superior physicochemical and acidic properties, the Ni/HZ-0.5 M catalyst exhibited outstanding catalytic activity (100% conversion, TOF 7.12 h−1) and menthol selectivity (83%, 4 h) with uniform stability at 100 °C, 1.0 MPa hydrogen. Similarly, the cracking rate decreased with the decrease in Bronsted acid sites.

Herein, polymeric cryogels containing poly(N-isopropylacrylamide) were synthesized by cryo-polymerization at subzero temperature. The synthesized cryogels were loaded with silver and palladium nanoparticles by the chemical reduction method at room temperature using the reducing agent NaBH4. Moreover, for comparison with cryogels, pure poly(N-isopropylacrylamide) hydrogel and its silver hybrid were also prepared by the conventional method at room temperature. The chemical structure and functional group analysis of the pure cryogels was confirmed by Fourier transform infrared spectroscopy. The synthesis of hybrid cryogels was confirmed by the X-ray diffraction technique and energy dispersive X-ray. The pore size and surface morphology of the pure cryogels, their respective hybrid cryogels and of conventional hydrogels were studied by using the scanning electron microscopy technique. The hybrid cryogels were successfully used as a catalyst for the degradation of methyl orange dye. The degradation performance of the hybrid cryogels was much better than its counterpart hybrid hydrogel for methyl orange dye. The effect of temperature and amount of catalyst on catalytic performance was studied by UV-visible spectroscopy. The reduction follows pseudo-first-order reaction kinetics. In addition, the antibacterial activities of these cryogels were evaluated against Gram-positive bacteria (Staphylococcus aureus, ATCC: 2593) and Gram-negative bacteria (Escherichia coli, ATCC: 25922). Both hybrid cryogels have shown much better antibacterial activity for these two strains of bacteria compared to pure cryogels. The results indicate that these cryogels are potential candidates for water purification systems as well as biomedical applications.

Aluminum nitride (AlN) is a semiconductor material possessing a hexagonal wurtzite crystal structure with a large band gap of 6.2 eV. AlN thin films have several potential applications and areas for study, particularly in optoelectronics. This research study focused on the preparation of Ni-doped AlN thin films by using DC and RF magnetron sputtering for optoelectronic applications. Additionally, a comparative analysis was also carried out on the as-deposited and annealed thin films. Several spectroscopy and microscopy techniques were considered for the characterization of structural (X-ray diffraction), morphological (SEM), chemical bonding (FTIR), and emission (PL spectroscopy) properties. The XRD results show that the thin films have an oriented c-axis hexagonal structure. SEM analysis validated the granular-like morphology of the deposited sample, and FTIR results confirm the presence of chemical bonding in deposited thin films. The photoluminescence (PL) emission spectra exhibit different peaks in the visible region when excited at different wavelengths. A sharp and intense photoluminescence peak was observed at 426 nm in the violet-blue region, which can be attributed to inter-band transitions due to the incorporation of Ni in AlN. Most of the peaks in the PL spectra occurred due to direct-band recombination and indirect impurity-band recombination. After annealing, the intensity of all observed peaks increases drastically due to the development of new phases, resulting in a decrease in defects and a corresponding increase in the crystallinity of the thin film. The observed structural, morphological, and photoluminescence results suggest that Ni: AlN is a promising candidate to be used in optoelectronics applications, specifically in photovoltaic devices and lasers.

There are two common categories of implants that are used in medical sciences, i.e., orthopedic and dental ones. In this study, dental implant materials are focused such as Ti6Al4V alloys that are used for the replacement of lost teeth due to their high strength and biocompatibility. However, they cause infections in nearby tissues due to elemental release (potentially Al and V). Thus, manganese is selected to be incorporated into the alloy since it is also present in the human body in the form of traces. Different sets of implants were produced, i.e., Ti5Mn and Ti10Mn (where 5 and 10 describe the percentage of Mn) by using the powder metallurgy technique. This was followed by characterization techniques, including X-ray fluorescence spectroscopy (XRF), X-ray diffractometer (XRD), optical microscope (OM), and nanoindenter. The very aim of this study is to compare the microstructural evolutions, density, and mechanical properties of reference alloys and the ones produced in this study. Results show the microstructure of Ti6Al4V consists of the alpha (α) and beta (β) phases, while Ti5Mn and Ti10Mn revealed the beta (β) phases. The Ti5Mn alloy showed excellent mechanical properties than that of the Ti6Al4V counterpart. Extensive discussion is presented in light of the observed results. The relative density of Ti5Mn alloy was found to be enhanced than that of reference alloy.

Wastewater from the textile industry is chronic and hazardous for the human body due to the presence of a variety of organic dyes; therefore, its complete treatment requires efficient, simple, and low cost technology. For this purpose, we grew ZnO microstructures in the presence of psyllium husk, and the role of psyllium husk was to modify the surface of the ZnO microstructures, create defects in the semiconducting crystal structures, and to alter the morphology of the nanostructured material. The growth process involved a hydrothermal method followed by calcination in air. Additionally, the psyllium husk, after thermal combustion, added a certain value of carbon into the ZnO nanomaterial, consequently enhancing the photocatalytic activity towards the degradation of methylene blue. We also investigated the effect of varying doses of photocatalyst on the photocatalytic properties towards the photodegradation of methylene blue in aqueous solution under the illumination of ultraviolet light. The structure and morphology of the prepared ZnO microstructures were explored by scanning electron microscopy (SEM) and powder X-ray diffraction (XRD) techniques. The degradation of methylene blue was monitored under the irradiation of ultraviolet light and in the dark. Also, the degradation of methylene blue was measured with and without photocatalyst. The photodegradation of methylene blue is highly increased using the ZnO sample prepared with psyllium husk. The photodegradation efficiency is found to be approximately 99.35% for this sample. The outperforming functionality of psyllium-husk-assisted ZnO sample is attributed to large surface area of carbon material from the psyllium husk and the synergetic effect between the incorporated carbon and ZnO itself. Based on the performance of the hybrid material, it is safe to say that psyllium husk has high potential for use where surface roughness, morphology alteration, and defects in the crystal structure are vital for the enhancing the functionality of a nanostructured material. The observed performance of ZnO in the presence of psyllium husk provides evidence for the fabrication of a low cost and efficient photocatalyst for the wastewater treatment problems.

This paper aimed to study the effect of aqueous, aqueous polyethylene glycol (1.0 %w/v) and aqueous polyvinyl pyrrolidone (1.0 %w/v) on the physicochemical behaviour of three pharmaceuticals substantial drugs by viscosity method. Viscosity measurements of the drugs (chloroquine phosphate, acefylline piperazine and gentamicin sulfate) solutions were performed within concentration ranges from 2.0 × 10−2 to 10.0 × 10−2 ± 0.001 mol.dm−3 at varying temperatures (293.15, 298.15, 303.15, 308.15, 313.15 and 318.15 ± 0.01 K). The viscosity data used to interpret the interactions (drug-drug and drug-solvent) existing in the solutions of drugs in terms of ‘A’ and ‘B’ coefficients of Jones–Dole equation respectively. Temperature derivatives of the B-coefficient (dB/dT) were also calculated which help to establish the relation between the nature of the solute and the structural modifications in the solution. Hence, the structure promoting ability of the AP in aqueous system and structure destroying effect of CP, AP and GS in the aqueous-polymeric system was observed. The FTIR studies of CP, AP and GS show that the chemical identity of the drug was not affected by the polymers and no binding of the new forming compound was detected.

From last epoch till to date, AISI 4340 and AISI 4140 have been widely used in different engineering applications. These applications include bolt, screws, gears, drive shafts, crane shaft and piston rods for engines due to its upright mechanical properties, cost-effective and easily available in market. In present work, deep cryogenic treatment effect on the mechanical properties of AISI 4340 and AISI 4140 have been studied. Present work was carried out at laboratory scale and can be extended for mass production. Our work is simple, straight forward safe and economical. In our work, samples were heat treated in simple muffle furnace and followed by cryogenic treatment in liquid nitrogen. Before cryogenic treatment, all samples were normalized at 860°C to obtain homogenized microstructure. Samples were also compared conventionally heat treatment with quenched in oil quenchant. Experimental results showed that after cryogenic treatment with tempering treatment, one could easily increase the tensile strength, impact toughness and hardness. Advanced optical microscopy (IMM 901) and SEM (Scanning Electron Microscopy), FIT Quanta 200 methods have also been deployed to reveal and interpret the internal structure of samples. It was found from microstructure that cryogenic treated sample increases the impact strength, hardness and tensile strength as compared conventional heat treated quenching approaches.

Aluminum alloys have been attracted by several engineering sectors due to their excellent strengthweight ratio and corrosion resistant properties. These are categorized into 1, 2, 3, 4, 5, 6, 7and 8xxx on the basis of alloying elements. Among these 6xxx series contains aluminum–magnesium–silicon as alloying elements and are widely used in extruded products and automotive body panels. The major advantages of these alloys are good corrosion resistance, medium strength, low cost, age hardening response no yield point phenomenon and Ludering. 6xxx series alloys generally have lower formability than other aluminum alloys which restrict their utilization for wide applications. Keeping in view of the shortcomings in the set of mechanical properties of 6xxx series the efforts were made to improve the tensile strength and toughness properties through age hardening. In present study heat treatment cycles were studied for 6061 aluminum alloy. Three different age hardening temperatures 160, 200 and 240oC were selected. The obtained results showed that 17.26, 7.69, and 10.51% improvement in tensile strength, toughness and hardness respectively was achieved with solution treatment at 380oC followed by an aging 240oC. Microstructural study revealed that substantial improvements in the mechanical properties of 6061 aluminum alloy under heat treatment were achieved due to precipitation of Mg2Si secondary phase.

The present study describes the use of a leaf extract from Ficus carica as a source of natural antioxidants for the surface alteration of bulk titanium dioxide (TiO2) in two steps. First, the hydro-thermal treatment of the bulk TiO2 material was carried out and followed by thermal annealing at 300 °C for 3 h in air. The role of the leaf extract of Ficus carica on the performance of the bulk TiO2 material for the removal of methylene blue (MB) was also studied. Various analytical techniques such as powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) were used to explore the crystalline structure, morphology, and composition. The bulk TiO2 material after the leaf-extract treatment exhibited mixed anatase and rutile phases, a flower-like morphology, and Ti, O, and C were its main elements. The average crystallite size was also calculated, and the obtained values for the bulk TiO2 material, 18.11 nm, and the treated bulk TiO2 material with various amounts, 5, 10, and 15 mL, of leaf extract were 16.4, 13.16, and 10.29 nm respectively. Moreover, Fourier-transform infrared spectroscopy validated the typical metal–oxygen bonds and strengthened the XRD results. The bulk TiO2 material chemically treated with Ficus carica has shown outstanding activity towards the degradation of MB under sunlight. The 15 mL of Ficus carica extract significantly enhanced the photocatalytic activity of the bulk TiO2 material towards the degradation of MB. The dye degradation efficiency was found to be 98.8%, which was experimentally proven by the Fourier Transform Infrared spectroscopoyy (FTIR) analysis. The obtained performance of the bulk TiO2 material with Ficus carica revealed excellent surface modifying properties for poorly-performing photocatalysts towards the degradation of synthetic dyes when used in their pristine form. The presented approach suggests that Ficus carica could be of great interest for tuning the surface properties of materials, either in the form of nano-size or bulk-phase in a particular application.

The majority of food packaging materials are petroleum-based polymers, which are neither easily recyclable nor ecologically friendly. Packaging films should preferably be transparent, light in weight, and easy to process, as well as mechanically flexible, and they should meet the criteria for food encapsulation. In this study, poly (vinyl alcohol) (PVA)-based films were developed by incorporating glass flakes into the films. The selection of PVA was based on its well-known biodegradability, whereas the selection of glass flakes was based on their natural impermeability to oxygen and moisture. The films were processed using the blade coating method and were characterized in terms of transparency, oxygen transmission rate, mechanical strength, and flexibility. We observed that the incorporation of glass flakes into the PVA matrix did not significantly change the transparency of the PVA films, and they exhibited a total transmittance of around 87% (at 550 nm). When the glass flakes were added to the PVA, a significant reduction in moisture permeation was observed. This reduction was also supported and proven by Bhardwaj’s permeability model. In addition, even after the addition of glass flakes to the PVA, the films remained flexible and showed no degradation in terms of the water vapor transmission rate (WVTR), even after bending cycles of 23,000. The PVA film with glass flakes had decent tensile characteristics, i.e., around >50 MPa. Increasing the concentration of glass flakes also increased the hardness of the films. Finally, a piece of bread was packaged in a well-characterized composite film. We observed that the bread packaged in the PVA film with glass flakes did not show any degradation at all, even after 10 days, whereas the bread piece packaged in a commercial polyethylene bag degraded completely. Based on these results, the developed packaging films are the perfect solution to replace commercial non-biodegradable films.

This research aims to study the variation in properties of hot-rolled SAE 1006 IF steel sheets during cold rolling to reveal the factors causing the decrease in formability of SPCG steel sheets during deep drawing. Results have shown that pickling does not affect the mechanical properties; however, cold rolling results in an increase in hardness, tensile strength and yield strength. Stress relieve annealing results in coarsening and homogenizing of grains which reduces brittleness and impart ductility. Temper rolling causes an increment in mechanical parameters again, improve surface hardness and flatness. By analyzing the microstructure and comparing it with the HESCO sample, it is revealed that there are still some elongated grains found along with coarse grains after annealing. Soaking time is not sufficient for the growth of homogenized structure, resulting in decreased ductility and formability during deep drawing.

The βNiAl coating was deposited onto Nickel based CMSX-4 superalloy by in-situ CVD (Chemical Vapor Deposition) method. Main focus of this contribution was to study the influence of aluminizing time and temperature on the microstructure and thickness of the coating; this was followed by examination by XRD (X-Ray Diffraction), electron microscope. Results suggest that an incremental variation in temperature alters the coating activities from HA (High Activity) to LA (Low Activity). This is exhibited by the resultant CT (Coating Thickness) since HA coatings are thicker than LA counterparts. The microstructure of the coating formed at low temperature (or HA ones) showed a large amount of α-Cr precipitates while one formed at high temperature (or LA ones) exhibited lower amounts of such precipitates. Moreover, incremental aluminizing time showed linear trend of CT at initial stage, thereafter (10 hrs) it leveled off. Whereas it does not affect microstructure of the coating

CHQ (Cold Heading Quality) steels are assumed to be non-heat treatable so strengthened by cold forming which is a quick and mass production makes it low cost manufacturing process. In this study, microstructure and phase transformation in steels is a fundamental aspect of governing the properties. A large number of studies are dedicated on the subject phase transformations owing to availability of several commercial steel grades. Due to several grades of steels commercially available shows differently behavior so it is hard to conclude that phase transformation is universally understood completely. In this study the influence of heating rate on the development of microstructure of CHQ steel has been studied thoroughly by using different heating techniques.For characterization, optical microscope connected with high resolution camera and SEM (Scanning Electron Microscope) was utilized to interpret the microstructural results. In addition, heat treatment methods have been utilized as to vary the microstructure in the steel under experimentation. It was found that heating rate could have major effect on phase transformation of CHQ steel (under study). Rate of heating enhances the austenite development kinetics with respect to dwell time and such austenite has been changed to martensite upon cooling. In addition, heating rate also promotes nucleation sites for the formation of austenite phase of CHQ steel.

Sacrificial anodes possessing higher electrochemical efficiency is the demand of marine, oil and gas industries. Due to high energy capability and long life light weight aluminum based anodes are more favorable as compare to magnesium and zinc based anodes to protect the engineering structures from corrosion. In present study an attempt was made to develop Al-5% Zn based composite with nano-ceria. The effect of nano-ceria on physiognomies of Al-5% Zn anode was determined through weight loss, CPR (Corrosion Penetration Rate) and emf study in CCP (Close Circuit Potential) conditions. The results indicated that by incorporating the ceria in the matrix of Al-5% Zn anode the corrosion inhibition efficiency and hardness were increased significantly.

In hybridization different fibers are stacked layer by layer to produce laminates have specific strength and stiffness and employed in light weight high strength applications. Physically mean fabricated hybrid composites used in aerospace, under water, body armors and armed forces establishment. In present work drop-weight impact response of hybrid composites were investigated by making laminates of hybrid composites. In Hybridization layers of E-glass (roving) and Kevlar 49 fabrics stacked with epoxy resin. The layers formulation was set up by hand layup method. Impregnationsof epoxy resin of commercial grade (601A) in fabrics were accomplished by VRTM (Vacuum Bagging Resin Transfer Molding) technique. Layup placementof Glass fibers/ Kevlar at 0°/90°, 45°/45° and 30°/60° were set for this work. Mechanical properties such as impact strength, bear resistance and break resistance were analyzed by usingASTM D-256 and D-3763 standard.Experimental investigation was conducted using instrumented Dart impact and Izod Impact test. E-glass/Kevlar 49 at layup 0°/90°and 30°/60°exhibited improvedimpact strength than 45°/45°. The surface morphology and fractography were also investigated by capturing different images of Specimens by using the SEM (Scanning Electron Microscopy). The fiberreinforcement and matrix fracture were also observed by using SEM.The SEM images suggest that epoxy resin tightly bonded with Kevlar fibers whereas Glass fibers were pulled out from laminations.

Plasmonic materials are the artificially manufactured materials (metamaterials) typically composed of nanostructure noble metals which give the unique optical properties superior to naturally occurring materials. Such plasmonic material has ability to give surface plasmon when electromagnetic light wave interact with free electrons in conduction band of the noble metals. Entirely absorption of light wave is the one of the major property of such plasmonicmetamaterials. Recently, these metamaterials has drawn the attention of scientists because of its wide range of applications in harvesting energy and sensors. These applications are strongly dependent on adjusting the absorption band-width, peak position and absorption intensity. In this work we show that using ultra-thin multicomponent (i.e. Au NPs incorporated in mixture of SiO2 and TiO2 matrix) nanocomposite deposited on optically thick gold film through subsequent magnetron sputtering. Experimental results show that one can broaden the bandwidth and peak position to span Ultraviolet up to near infrared wavelength range

Martensitic stainless steels are commercially significant materials owing to the remarkable properties they offer because of their martensitic structure during application. The paper aimed to investigate the effects of tempering temperature on mechanical properties and microstructure. Determination of carbide morphology was also included in the study to substantiate the results. This study used AISI 420 samples of 10 mm thickness, hardened at 1050oC and then subjected to tempering treatment at temperatures: 150oC, 250oC, 350oC, 450oC, 550oC and 650oC. Each sample was oil quenched after a soaking time of 25 minutes. Optical Microscopy and Scanning Electron Microscopy was conducted to examine the changes in the microstructure and the morphology of carbides. The results have shown that at various temperatures during tempering there is subsequent increase in toughness where hardness decreases and vice versa. Matrix of martensite contains some carbide precipitates. Due to Temper embrittlement occurring between 350°C-450oC, toughness has been decreased as a result of secondary hardening between the temperatures of 450°C-550°C, hardness has been increased drastically.

Corrosion is one of the major problems of mild steels in acidic medium. This can be minimized by the application of corrosion inhibitors, however; the most of inhibitors are toxic in nature. Therefore inhibitors from green sources are highly desirable to maintain the sustainability of the environmental system. Consequently, in this study ginger was selected; its juice extracted mechanically and used as an inhibitor. The different concentrations of ginger extract such as 0.25ml, 0.5ml, 0.75ml and 1ml were mixed in 0.1 M HCl solution to record the effect of inhibitor on corrosion rate at room temperature and at an elevated temperature of 50ᵒC. Electrochemical linear polarization resistance (LPR) tests were carried out to determine the corrosion rates at both temperatures with different additions of the inhibitor respectively. The LPR test uses three electrodes, first electrode of AISI 1019 (mild steel), second electrode is standard electrode of saturated calomel while the third electrode consists of graphite, which is called counter electrode, to measure potential difference. The whole assembly was dipped in the solution having varying concentration of inhibitors. The corrosion rate was found to be higher in the absence of ginger- extract. Conversely, the corrosion rate was dramatically reduced more prominently at 50oC but was less effective at Troom; with the trace-additions of ginger-inhibitor. So this research would be the good contribution to overcome the deterioration of mild steel and increase its life at ambient temperatures, by using economically available environmentally-friendly organic compound specially the use of locally available raw material should be focused.

Different compositions of Si-Ge nanowires (SGNWs) have been fabricated by Vapor Liquid Solid (VLS) mechanism by using Ni as a catalyst with different SiCl4: GeCl4 ratios and temperatures respectively. The SEM results show that the SGNWs could be grown successfully vertical on the surface of the silicon with temperatures of 1000oC, 950oC, 900oC and 850oC. But for 900oC and 850oC, some of the NWs were observed to be grown as flower like structures instead of vertical. The growth rates are observed to be depending upon the ratio and the flowing times of the precursors greatly. For equal ratio of precursors (SiCl4: GeCl4=1:1) and the precursors’ flowing times of 5 min and 10 min, the growth rates of the SGNWs were observed to be around 20um/min and 30um/min respectively. The SEM results showed that the SGNWs could be grown successfully, vertical on the surface of the silicon with varying temperatures. Keywords: SiGe Nanowire, growth rate, optical characteristics.