The electromagnetic pulse (EMP) is a destructive phenomenon which harms the building, telecommunication, and IT based infrastructure. Thus, it is required to reduce the effect of EMP using shielding materials. In the present study, we have used different thickness of concrete walls by incorporating 1 and 5 wt% of carbon black, as well as 100 µm thick Zn–Al coating using the arc thermal metal spraying method (ATMSM). The EMP was evaluated using waveguide measurement fixture for shielding performance of the concrete wall in the range of 0.85 to 1 GHz frequency. The results reveal that the maximum value, i.e., 41.60 dB is shown by the 5-300-N specimen before application of Zn–Al coating where the thickness of concrete wall was 300 mm and 5% carbon black. However, once the 100 µm thick Zn–Al coating was applied on concrete specimen, this value was increased up to 89.75 dB. The increase in shielding values around 48 dB after using the Zn–Al coating is attributed to the reflection loss of the metal thermal spray coating. Thus, the Zn–Al coating can be used for EMP application instead of metallic plate.

In the present study, different amounts, i.e., 1–3 v/v% of 1 M ammonium phosphate monobasic, were used as an eco-friendly corrosion inhibitor to mitigate the corrosion of steel rebar exposed to simulated concrete pore (SCP) + 3.5 wt% NaCl solution at a prolonged duration. Potentiodynamic polarization results show that as the amount of inhibitor is increased, the corrosion resistance of steel rebar is increased. The steel rebar exposed to 3% inhibitor-containing SCP + 3.5 wt% NaCl solution exhibited nobler corrosion potential (Ecorr), the lowest corrosion current density (icorr), and 97.62% corrosion inhibition efficiency after 1 h of exposure. The steel rebars exposed to 3% inhibitor-containing SCP + 3.5 wt% NaCl solution revealed higher polarization resistance (Rp) and film resistance (R0) with exposure periods compared to other samples owing to the formation of passive film. The scanning electron microscopy (SEM) of steel rebar exposed to 3% inhibitor-containing SCP + 3.5 wt% NaCl solution showed homogenous and uniform dendritic passive film which covers all over the surface, whereas, bare, i.e., SCP + 3.5 wt% NaCl solution exposed samples exhibited pitting and irregular morphology. Raman spectroscopy results confirm the formation of goethite (α-FeOOH), maghemite (γ-Fe2O3), and iron phosphate (FePO4) as a passive film onto the steel rebar surface exposed to 3% inhibitor-containing SCP + 3.5 wt% NaCl solution. These phases are responsible for the corrosion mitigation of steel rebar which are very protective, adherent, and sparingly soluble.

The present study has been focused on the environment-friendly corrosion inhibitor. Conifer cone (Pinus resinosa) has been used as a novel corrosion inhibitor to mitigate the corrosion of steel rebars in simulated concrete pore solutions (SCPS) in the presence and absence of chloride ions. The corrosion inhibitor is extracted by simple chemical methods. The functional groups present in the extracted conifer cone (ECC) powder are characterized as well as the surface morphology of ECC has been examined. The corrosion inhibition performance has been evaluated by the electrochemical and weight loss methods. The experimental results indicate that ECC possesses a corrosion inhibition efficiency of 81.2% at a dosage of 1000 mg·L–1, after 720 h of immersion in chloride-contaminated SCPS. Adsorption isotherm and their standard Gibbs free energy (ΔG ads 0) values are calculated by Langmuir, Freundlich, and Temkin isotherm methods, and the results indicate that the ECC is initially adsorbed on the steel rebar surface by physisorption and then it turns to chemisorption. The steel rebar surfaces have been characterized after exposure to the ECC containing SCPS, and the results indicate that the ECC containing cationic adsorbate molecules, which interact with steel rebar, leads to retardation of metal dissolution in corrosive chloride medium.

This paper reports the crystallization kinetics of (Cu60Zr25Ti15)99.3Nb0.7 bulk metallic glass under isothermal conditions. Differential scanning calorimetry (DSC) has been employed for isothermal annealing at ten different temperatures prior to the onset of crystallization (To) temperature. X-ray diffraction and transmission electron microscopy have been used to confirm the amorphous structure of the as cast sample. Crystallized volume fractions (x) are calculated from the exothermic peaks of DSC scans. Crystallized volume fractions (x) against time show sigmoidal type of curves as well as the curves become steeper at higher annealing temperatures. Continuous heating transformation diagram has been simulated to understand the stability of the bulk metallic glass. Crystallization kinetics parameters are calculated using Arrhenius and Johnson–Mehl–Avrami equations. Activation energy (Ea) and Avrami exponential factor (n) have exhibited strong correlation with crystallized volume fraction (x). The average activation energy for isothermal crystallization is found to be 330 ± 30 kJ/mol by Arrhenius equation. Nucleation activation energy (Enucleation) is found to be higher than that of growth activation energy (Egrowth). The Avrami exponential factor (n) indicates about the diffusion controlled mechanism of the nucleation and three-dimensional growth.

In the present study, different contents, i.e., 1–3% of 0.5 M ammonium phosphate mono basic (APMB), were used as corrosion inhibitor to reduce the corrosion of steel rebar. Electrochemical impedance spectroscopy (EIS) results showed that up to 24 h of exposure, polarization resistance (Rp) and passive/oxide film resistance (Ro) gradually decreased in simulated concrete pore (SCP) + 3.5 wt.% NaCl solution owing to the reduction in pH of the solution. The steel rebar exposed in 2% inhibitor containing SCP + 3.5 wt.% NaCl solution exhibited 90% inhibition efficiency after 1 h of exposure. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the formation of thermodynamically very stable and sparingly soluble goethite (α-FeOOH), maghemite (γ-Fe2O3), and iron phosphate (FePO4) as passive/oxide film onto the steel rebar surface exposed to 2% inhibitor containing SCP + 3.5 wt.% NaCl solution.

Ground granulated blast furnace slag (GGBFS) conventionally has been incorporated with ordinary Portland cement (OPC) owing to reduce the environmental load and enhance the engineering performance. Concrete with GGBFS shows different strength development of normal concrete, but sensitive, to exterior condition. Thus, a precise strength evaluation technique based on a quantitative model like full maturity model is required. Many studies have been performed on strength development of the concrete using equivalent age which is based on the apparent activation energy. In this process, it considers the effect of time and temperature simultaneously. However, the previous models on the apparent activation energy of concrete with mineral admixtures have limitation, and they have not considered the effect of temperature on strength development. In this paper, the apparent activation energy with GGBFS replacement ratio was calculated through several experiments and used to predict the compressive strength of GGBFS concrete. Concrete and mortar specimens with 0.6 water/binder ratio, and 0 to 60% GGBFS replacement were prepared. The apparent activation energy (Ea) was experimentally derived considering three different curing temperatures. Thermodynamic reactivity of GGBFS mixed concrete at different curing temperature was applied to evaluate the compressive strength model, and the experimental results were in good agreement with the model. The results show that when GGBFS replacement ratio was increased, there was a delay in compressive strength.

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Lauric acid (LA) has been recommended as economic, eco-friendly, and commercially viable materials to be used as phase change materials (PCMs). Nevertheless, there is lack of optimized parameters to produce microencapsulated PCMs with good performance. In this study, different amounts of LA have been chosen as core materials while tetraethyl orthosilicate (TEOS) as the precursor solution to form silicon dioxide (SiO2) shell. The pH of precursor solution was kept at 2.5 for all composition of microencapsulated LA. The synthesized microencapsulated LA/SiO2 has been characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-Ray photoelectron spectroscopy (XPS), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM). The SEM and TEM confirm the microencapsulation of LA with SiO2. Thermogravimetric analysis (TGA) revealed better thermal stability of microencapsulated LA/SiO2 compared to pure LA. PCM with 50% LA i.e. LAPC-6 exhibited the highest encapsulation efficiency (96.50%) and encapsulation ratio (96.15%) through Differential scanning calorimetry (DSC) as well as good thermal reliability even after 30th cycle of heating and cooling process.