This study involves the investigation of altering the photocatalytic activity of TiO2 using composite materials. Three different forms of modified TiO2, namely, TiO2/activated carbon (AC), TiO2/carbon (C), and TiO2/PANi, were compared. The TiO2/carbon composite was obtained by pyrolysis of TiO2/PANi prepared by in situ polymerization method, while the TiO2/activated carbon (TiO2/AC) was obtained after treating TiO2/carbon with 1.0 M KOH solution, followed by calcination at a temperature of 450°C. X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FTIR), thermogravimetric analysis (TG-DTA), Brunauer-Emmet-Teller (BET), and UV-Vis spectroscopy were used to characterize and evaluate the prepared samples. The specific surface area was determined to be in the following order: TiO2/AC > TiO2/C > TiO2/PANi > TiO2 (179 > 134 > 54 > 9 m(2) g(-1)). The evaluation of photocatalytic performance for the degradation of methylene blue under UV light irradiation was also of the same order, with 98 > 84.7 > 69% conversion rate, which is likely to be attributed to the porosity and synergistic effect in the prepared samples.
Iron (III) oxide, a stable semiconductor with versatile applications, was synthesized alongside Sn-doped Fe2O3 (Sn-Fe2O3) using the sol-gel technique. Characterization via X-ray diffraction, field-emission scanning electron microscopy, and UV-visible spectroscopy confirmed the presence of α- and γ-Fe2O3 phases in the synthesized powders. Incorporation of the dopant reduced the initial band gap energy of Fe2O3 (2.2 eV) by approximately 0.1 eV. To evaluate photocatalytic performance, Fe2O3 and Sn-Fe2O3 were tested for decolorization efficiency of a methyl orange solution. Results revealed the 5 wt% Sn-doped catalyst as optimal, achieving complete degradation of methyl orange within 120 min under simulated solar light. The addition of small amounts of Sn effectively reduced the Fe2O3 band gap and significantly enhanced photocatalytic performance. Investigation of pH and dye concentration impact on photocatalytic degradation revealed superior activity under acidic conditions compared to alkaline. Furthermore, maintaining a moderate concentration of methyl orange (10 ppm) ensured optimum photocatalytic activity.
Due to growing environmental concerns and regulations limiting the use of harmful and toxic synthetic corrosion inhibitors, there is a high demand for sustainable corrosion inhibitors. In this study, a green and rapid technique was used to synthesize amide N-(4-aminobutyl)palmitamide (BAPA) which yielded 91.17% of the product within 2 min, compared to a low yield of 75-80% and a very long 8-10 h reaction time with the conventional thermal condensation method. The chemical structure of BAPA was analyzed by FT-IR, 1HNMR and 13CNMR spectra, as well as CHNS elemental analysis. When applied to mild steel exposed to 1 M HCl, BAPA delayed and reduced corrosion by adsorbing to the steel surface to form a protective layer. The inhibition efficiency increased with increasing amide concentration, and maximal inhibition of 91.5% was observed at 0.5 mM BAPA. The adsorption of BAPA on mild steel in an acidic solution was studied and inhibition performance was correlated with the calculated adsorption-free energy ΔGads, indicating good agreement between the experimental and adsorption findings. Surface morphology of untreated and treated mild steel coupons was evaluated by SEM, and based on density functional theory (DFT) computations and atomic charges analysis, a stronger interaction was observed between BAPA and mild steel surface leading to the formation of a compact protective film on the metallic surface. This protective film is attributed to the presence of nitrogen atoms and carbonyl group in the chemical structure of BAPA.
In the recent decades, the researchers have been focused on the use of photovoltaic thermal (PVT) systems that provide the best performance and cooling for the photovoltaic panels. In this study, a PVT system consisting of a monocrystalline PV panel and a spiral heat exchanger was connected to an underground heat exchanger that is buried at a depth of 4 m below the surface of the earth. The procedure of the current study can be considered the first of its kind in the Middle East and North Africa region (based on the researchers' knowledge). The study was carried out on agricultural land in Baghdad-Iraq during months of July and August-2022, which are considered the harshest weather conditions for this city. The heat exchanger consists of a copper tube with a length of 21 m and formed in the shape of 3U, and it was buried in the earth and connected with a PVT system. The results of the study showed that the site chosen to bury the heat exchanger (4 m deep) has a stable soil temperature at 22.5 °C. From various volumetric flow rates, a flow rate of 0.18 l/s was selected which is considered the highest flow rate that can show vibration in the PVT system which may harm the system. The practical measurements showed that the largest difference in the surface temperatures of standalone PV and PVT was around 20 °C in favor of the latter. The electrical efficiency of the studied PVT system also increased to outperform the standalone PV system by 127.3%. By comparing the results of the current study with studies of water-cooled PVT systems from the literature, it is clear that the proposed system is feasible and has an acceptable efficiency in such harsh weather conditions tested during the experiment.