Iranian Journal of Materials Science and Engineering

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Abstract: The performance of an Imidazoline based commercial corrosion inhibitor in CO2 corrosion of a gas-well tubing steel was studied by employing Electrochemical Impedance Spectroscopy (EIS) technique. Inhibitor performance was investigated by means of its efficiency at various concentration and also its behavior at various exposure time. EIS results showed that inhibitor interaction to the electrode surface obeys Lungmuir adsorption isotherm. Interpretation of some parameters such as Rct, Rpf, Cdl, and Cpf associated to the equivalent circuit fitted to the experimental rsults showed that not only inhibitor efficiency and surface coverage improve by increasing in inhibitor concentration in the solution but also at constant inhibitor concentration both surface coverage and efficiency improve with exposure time and reach to their highest value after 4 hours.

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In this study, the effect of different parameters such as time and temperature of calcination and milling on the formation of calcium aluminosilicates was investigated. Raw materials used in this study were calcium carbonate and kaolin in high purity. Powder X-ray diffraction patterns were obtained from all samples after heat treatment at various temperatures and times. To study the microstructure scanning electron microscope was used. Milling the samples contributed to the amorphous structure due to inducing defects in the structure. Moreover, increasing the milling time reduced crystallization temperature of anorthite. Uptake experiments were performed using solutions containing different concentrations of nickel. Samples were exposed to the solution for 24 h with stirring then the samples were filtered and the concentrations of the cations in the separated solutions were analyzed. FTIR analysis was conducted on the adsorbents before and after nickel uptake. Nevertheless, they hardly helped understand sorption mechanisms. Therefore, adsorption isotherms were studied instead. Three adsorption isotherms of Langmuir, Freundlich and DKR were used to model sorption data. Results suggested monolayer sorption occurs on the surface of the adsorbent and sorption energy calculated by DKR model was 22.36 kJ/mol which can be described as a strong chemical adsorption mechanism

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The inhibition behavior of N,N′-bis(2,4,6-trihydroxyacetophenone)-propandiimine (THAPP) as an environmentally friendly Salen Ligand on the corrosion inhibition of mild steel was studied in alkaline solution (pH=10) containing 3% NaCl. Measurements were carried out using electrochemical and surface techniques. The experimental results suggested that this compound was an effective corrosion inhibitor for mild steel and the protection efficiency was increased with the increase in inhibitor concentration. Polarization curves indicated that this organic compound was a mixed-type inhibitor. Adsorption on the mild steel surface follows the Langmuir isotherm model. Activation parameters and thermodynamic adsorption parameters of the corrosion process such as E a , ΔH, ΔS, K ads , and ΔG ads were calculated by the obtained corrosion currents at different temperatures

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Jatropha curcas leaves extract was tested as a green corrosion inhibitor for mild steel in aqueous hydrochloric acid solution using gravimetric and thermometric techniques. The results reveal that the inhibition efficiency vary with concentration of the leaf extract and the time of immersion. Maximum inhibition efficiency was found to be 95.92% in 2M HCl with 0.5 g/l concentration of the extract in gravimetric method, while 87.04% was obtained in thermometric method. The inhibiting effect was attributed to the presence of alkaloids, flavonoids, saponins, tannins and phenol in the extract. The adsorption processes of the Jatropha curcas leaves extract onto the mild steel is consistent with the assumptions of Langmuir isotherm model and also found to be spontaneous. From the results, a physical adsorption mechanism is proposed for the adsorption of Jatropha curcas leaves extract onto mild steel surface.

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In this study, an  organic compound  inhibitor, namely N-benzyl-N-(4-chlorophenyl)-1H-tetrazole-5-amine (NBTA), was synthesized and the role of this inhibitor for corrosion protection of stainless steel (SS) exposed to 0.5 M H₂SO₄ was investigated using electrochemical, and quantum analysis. By taking advantage of potentiodynamic polarization, the inhibitory action of NBTA was found to be mainly mixed type with dominant anodic inhibition. The effectiveness of the inhibitor was also indicated using electrochemical impedance spectroscopy (EIS). Moreover, to provide further insight into the mechanism of inhibition, quantum chemical calculations of the inhibitor were performed. The adsorption of NBTA onto the SS surface followed the Langmuir adsorption model with the free energy of adsorption ΔG⁰_ads of of -7.88 kJ mol^-1. Quantum chemical calculations were employed to give further insight into the mechanism of inhibition action of NBTA.

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In this study, the adsorption of hexavalent chromium and zinc ions from the solution is investigated by raw red mud and mechanical-chemical activated red mud along with the possibility of selective reclamation of these ions from the solution. The mechanical-chemical activation of red mud was done by employing high-energy milling and subsequent acid treatment with HNO₃. Raw red mud (RRM) and mechanical-chemical activated red mud (MCARM) adsorbents were characterized with Fourier transform infrared spectroscopy (FTIR), X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscope (SEM), and Brunauer–Emmett–Teller (BET) methods. In order to determine the suitable adsorption conditions, effects of pH of the solution, amount of adsorption, temperature, and time of adsorption were investigated. It was found that the optimum pH for the adsorption of hexavalent chromium and zinc ions by MCARM adsorbent was 2 and 6, respectively. According to these pH values, MCARM had the ability to separately adsorb more than 95 and 79% of hexavalent chromium and zinc ions from the solution, respectively. Experimental results were in good agreement with Langmuir and Freundlich isotherms. By considering the kinetic models of adsorption, the kinetics of the adsorption of both ions followed the pseudo-second-order reaction model. It was also determined that almost 25.8 and 61.8% of the hexavalent chromium and zinc ions adsorbed in MCARM could be recovered

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The synthesed foam-shaped zeolite ZSM-5 material w:::as char:::acterized by X-ray diffraction (XRD), (FTIR) spectroscopy, scanning electron microscopy (SEM) and BET technique. The adsorption performances of the material were evaluated for the basic blue-41 dye removal. A maximum removed amount of 161.29 mg/g  at 323K was achieved. Experimental kinetic data of this new adsorbent fitted well the pseudo-second order model. The apparent diffusion coefficient values was in the range of 10^-12 cm²/s. The regeneration tests revealed that the adsorption efficiency of the foam-shaped zeolite was retained after three  regeneration runs, with a loss of 6% of the original adsorbed value.

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ABSTRACT
In this paper, novel Nanohybrid CuO-Fe₃O₄/Zeolite nanocomposites (HCFZ NCs) have been synthesized to improve the adsorption capacity and activity for removing the Arsenic and Lead cations from the contaminated water solutions. The nanohybrid 4, 10, and 20 -HCFZ NC samples were investigated by XRD, FT-IR, TEM, FESEM, EDX, and BET. The characterization results of these catalysts confirmed the presence of CuO and Fe₃O₄ NPs in nanospherical shapes as Nanohybrid Cu and Fe oxides on the zeolite surface. Notably, the 10-HCFZ NC sample showed the highest removal efficiency of harmful metallic pollutants from the water in comparison to the prepared neat zeolite, 4-HCFZ NC, and 20-HCFZ NC samples, with a percentage removal of (97.9 %) for Pb ions and (93.5 %) for As ions within 30 minutes (100 ppm). According to the adsorption isotherms results, R² values for the Langmuir isotherm were the highest, suggesting that the experimental results fit better the Langmuir isotherm model. Generally, according to the obtained results, there is a possibility of enhancing the efficiency of Nanohybrid CuO-Fe₃O₄/Zeolite NCs to remove Arsenic and Lead ions from polluted aqueous solutions.
 

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In this work, blast furnace slag (BFS) was used as an adsorbent material for the removal of Pb(II) ions in solution in batch mode. The physico-chemical analyzes used indicated that the BFS is essentially composed of silica, lime, and alumina. Its specific surface area corresponds to 275.8m²/g and its PZC is around 3.8.
The adsorption study indicated that the maximum amount of Pb(II) adsorbed under optimum conditions (agitation speed (V_ag): 150rpm; pH: 5.4; particle size (Øs): 300µm, T: 20°C) is 34.26mg/g after 50 minutes of agitation, and adsorption yield is best for feeble initial concentrations. The most appropriate isothermal model was that of Langmuir, and the adsorption speed was better characterized by the pseudo-second order kinetic model. The adsorption mechanism revealed that internal diffusion is not the only mechanism that controls the adsorption process; there is also external diffusion, which contributes enormously in the transfer of Pb(II) from solution to adsorbent. Thermodynamic study indicated that the Pb(II) adsorption on the blast furnace slag (BFS) was spontaneous, exothermic, and that the adsorbed Pb(II) is more ordered at the surface of the adsorbent. Finally, we estimate that BFS is a superb adsorbent for water containing Pb(II).
 

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The growth of industries, populations, and industrial activities includes environmental pollutants. Pollution causes problems such as reduced light transmission, anaerobic conditions, and complications such as allergies and cancer for humans and other living organisms. The adsorption method is one of the most attractive, and efficient methods for removing environmental pollutants such as pharmaceuticals. Among the standard methods for wastewater treatment, adsorption is more efficient than other methods and is more economical. They have a meager price. Adsorption of pollutants can be an excellent way to remove toxic substances from polluted waters and industrial effluents. In this review, pharmaceutical removal by adsorption process was reviewed in details.

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Rice husk carbon by-product from the industrial combustion is a promising source to produce a vast amount of activated carbon adsorbent. This research prepared rice husk-activated carbon adsorbent by varying the concentration of potassium hydroxide solution (5, 10, 15, 20 % w/v) and activation time (2, 4, 6, 8 hours). Fourier-transform infrared spectral characterization (FTIR) indicated a significant effect before and after activation, especially the presence of hydroxyl groups. Based on the iodine adsorption, the specific surface area of the produced-activated carbon was approximately 615 m²/g. Experimental results showed that increasing potassium hydroxide concentration and activation time increases the water vapor adsorption capacity of the activated carbon. Compared with the rice husk carbon, the KOH-activated carbon enhanced the water vapor adsorption capacity to 931%. In the adsorption observation, changing the temperature from 15 to 27 ℃ caused a higher water vapor uptake onto the activated carbon. Two adsorption kinetics (pseudo-first- and pseudo-second-order models) were used to evaluate the adsorption mechanism. This research found that rice husk-activated carbon performed a higher water vapor adsorption capacity than other adsorbents (silica gel, zeolite, and commercially activated carbon).