The dry erosion behavior of API-X120 pipeline steel was investigated, under the erosive interaction of aluminum oxide particulates, in a range of speed (43–167 m·s−1) and impact angle (30°–90°). Erosion behavior is characterized by surface profile measurement, weight loss measurement, and surface morphology analysis by SEM/EDX. Optical profilometry revealed that the eroded area increased with elevating speed of particles while the penetration depth increased with the increases in impact angle as well as particle speed. Percent weight loss and normalized erosion rate indicated that the lower impact angles and higher speeds led to higher materials loss and erosion. SEM analyses on various combinations of impact angles and particle speeds demonstrated the predominant erosion mechanism under those specific conditions; attributed to the intensity of the resolved components of the momentum vector horizontal or normal to the target metal surface under those conditions.
This work describes the preparation of novel fluorescent bentonite clay (BP), modified with carbon quantum dots nanomaterials (CDs), and its usage as lead removal platform, the CDs was prepared using graphitic waste serving as carbon source material via hydrothermal method, and the as obtained CDs were found to be fluorescent, in spherical shape, positively charged and smaller than 5 nm. Encouraged by their structure and photoluminescence feature, they were used hereafter as intercalants or surface modifiers, in order to make fluorescent bentonite nanocomposites. Bentonite was used as negatively charged model of aluminosilicate and reacted with the positively charged CDs. Interestingly, CDs were found to intercalate bentonite as judged from XRD patterns, and TEM. Indeed, the basal distance of bentonite clay d(001) shifted from 1.2 nm to 2.9 nm, after bentonite modification using the prepared carbon dots; moreover the XRD pattern of BP-CDs recorded in the some regions show some additional diffraction peaks along with those for bentonite. The peaks centered at 2Ѳ =27 degree allocated to the facets of graphitic-like carbon, originated from the introduced carbon dots inside bentonite galleries. The prepared materials were characterized by XPS, FTIR and fluorescence analysis. The obtained results indicate that CDs were successfully intercalated inside bentonite matrix and found to be stable over time. The BP-CD nanocomposites were finally used as efficient hybrid platform for led removal with and extraction efficiently of 95% under light condition, room temperature under alkaline conditions and after only 10 min of reaction.
Nickel-based alloys are usually used for a wide range of applications like petrochemical processing, oil and gas extraction, marine engineering and high temperature applications in power generation industry e.g., heat exchangers or turbine blades due to their excellent corrosion resistance and good mechanical properties. Nickel-based alloys are designed to resist high loading and severe corrosive environments during operations. The aim of this study is to investigate the effect of depositing copper nanoparticles of different sizes on top of the surface of different nickel-based alloys (e.g.alloys 825, 625 and 276) on their corrosion behavior in different electrolytes of different pH values and chloride and sulfide ions concentrations. The study included, electrochemical and non-electrochemical characterization techniques. Also, the surfaces of the corroded alloys were checked using optical and scanning electron microscopy, energy dispersive x-ray and atomic force microscopy.
Increasing CO2 emissions from industry has disastrous consequences for the environment. Effective utilization of CO2 as a carbon source can address the environmental challenges, and we can address the energy crisis caused by fossil fuel consumption. Electrochemical conversion of CO2 is a promising method recently gaining widespread popularity. Its high productivity, however, remains a major challenge. This work involved a facile novel preparation of a suitable CuO nanocomposite to reduce CO2 into useful fuels effectively. Hydrothermal synthesis was used to synthesize the nanocomposite. The synthesized NC's structure, morphology, and elemental analysis were evaluated using XRD, Raman spectroscopy, SEM, and TEM. ICP-OES analysis was performed to quantify Cu concentration in the CuO composite, confirming 98.6% of Cu of the prepared matrix. The cyclic voltammetry method has been used to study the electrochemical activity of NC for CO2 reduction. Additionally, the NMR & GC-MS analyses were performed to identify the product. Regarding CO2 reduction, the NC performed greatly better than the ordinary CuO. In addition, the NC exhibits high structural stability and durability, demonstrating its potential to reduce CO2 into fuels.
Abstract BackgroundFatty alcohol polyoxyethylene ether-7 (AEO-7), a non-ionic surfactant, has recently been receiving extensive attention from the ocean pipeline industry for its ability to inhibit corrosion. However, the present lack of information concerning the potential environmental toxicity of AEO-7, especially towards aquatic organisms, is a major impediment to its wider application. Here, we assess potential adverse effects of AEO-7 on zebrafish embryos employing a variety of assays, including (i) a mortality/survival assay which allowed the median lethal concentration (LC 50 ) to be calculated; (ii) a teratogenicity assay on the basis of which the no observed effect concentration (NOEC) was determined; and (iii) specific assays of cardiotoxicity, neurotoxicity (based on locomotion), hematopoietic toxicity (the level of hemoglobin as revealed by o-dianisidine staining) and hepatotoxicity (liver steatosis and yolk retention examined by staining with Oil Red O). ResultsAEO-7 caused mortality with a calculated LC 50 of 15.35 μg/L, which, according to the U.S. Fish and Wildlife Service (USFWS) Acute Toxicity Rating scale, should be considered “super toxic”. Although at its NOEC (0.8 μg/L), there were no signs of significant teratogenicity, cardiotoxicity, or hemopoiesis toxicity, 3.2 µg/L AEO-7 exerted dramatic detrimental effects on organ development. ConclusionOn the basis of these findings, we recommend that the industrial usage and environmental impact of AEO-7 be re-evaluated and strictly monitored by environmental and public health organizations.
A carbon nitride (C3N4) nanomaterial has superior mechanical, thermal, and tribological properties, which make them attractive for various applications, including corrosion-resistant coatings. In this research, newly synthesized C3N4 nanocapsules with different concentrations (0.5, 1.0, and 2.0 wt %) of ZnO as a dopant were incorporated into the NiP coating using an electroless deposition technique. The nanocomposite coatings either ZnO-doped (NiP-C3N4/ZnO) or undoped (NiP-C3N4) were heat-treated at 400 °C for 1 h. The as-plated and heat-treated (HT) nanocomposite coatings were characterized by their morphology, phases, roughness, wettability, hardness, corrosion protection, and antibacterial properties. The results indicated that the microhardness of as-plated and heat-treated nanocomposite coatings was significantly improved after the incorporation of 0.5 wt % ZnO-doped C3N4 nanocapsules. The outcomes of electrochemical studies revealed that the corrosion resistance of the HT coatings is higher than the corresponding as-plated ones. The highest corrosion resistance is achieved on the heat-treated NiP-C3N4/1.0 wt % ZnO coatings. Although the presence of ZnO in the C3N4 nanocapsules increased its surface area and porosity, the C3N4/ZnO nanocapsules prevented localized corrosion by filling the microdefects and pores of the NiP matrix. Furthermore, the colony-counting method used to evaluate the antibacterial behavior of the different coatings demonstrated superior antibacterial properties, namely, after heat treatment. Therefore, the novel perspective C3N4/ZnO nanocapsules can be utilized as a reinforcement nanomaterial in improving the mechanical and anticorrosion performance of NiP coatings in chloride media, together with providing superior antibacterial properties.
Halloysite nanotubes (HNTs) and their modifications with either NH2 (HNT-NH2) or NH2/Polypyrrole (HNT–NH2–PPy) were electroless-deposited into the NiP matrix for the first time to form NiP/HNT, NiP/HNT-NH2 and NiP/HNT–NH2–PPy nanocomposite coatings. The as-prepared nanocomposite coatings were heat-treated at 400 °C for 1 h. The transformation in microstructure, nanoindentation, Vicker's micro-hardness, surface morphology, and anti-corrosive properties of all prepared composite coatings were compared to the HNT-free (NiP) coating. Incorporating HNTs in the NiP coating made an appreciable enhancement in the hardness and corrosion resistance. Using the electrochemical impedance spectroscopy technique (EIS), the NiP/HNT-NH2 and NiP/HNT–NH2–PPy coatings showed more significant levels of enhancement in anticorrosion performance, offering about 16.5% and 25.4%, respectively, an increase in the inhibition efficiency of unmodified one (NiP/HNT), reached to 73 and 82%. Moreover, the modified HNT coatings revealed slightly high levels of betterment in microhardness, about 9% and 5.4% for HNT modification with NH2 and NH2-PPy, respectively. In addition, the heat treatment extra improved the hardness and the corrosion resistance of all HNTs nanocomposite coatings compared to HNT-free coating. Furthermore, the heat-treated NiP/HNT has the highest protection efficiency reached to about 95%, based on the polarization measurements. This momentous improvement in the hardness and electrochemical properties reflects the effect of adding the pristine and the modified HNTs into the NiP matrix, resulting in the development of high-performance NiP/HNT-NH2 and NiP/HNT–NH2–PPy composite coatings facilitating their use in various industries.
A ZnO-Fe-MXene nanocomposite was fabricated and examined with diverse spectroscopic techniques. The hexagonal structure of ZnO, MXene, and ZnO-Fe-MXene nanocomposites were validated through XRD. FTIR showed the characteristic vibrational frequencies of ZnO and MXene. The micrographs of the SEM showed nanoparticles with a flower-like structure. The electrocatalytic reduction efficiency of ZnO-Fe-MXene nanocomposite was analyzed through cyclic voltammetry and electrochemical impedance spectroscopy methods. The ZnO-Fe-MXene electrode was confirmed to have a high current density of 18.75 mA/cm2 under a CO2 atmosphere. Nyquist plots also illustrated a decrease in the impedance of the ZnO-Fe-MXene layer, indicating fast charge transfer between the Zn and MXene layers. Additionally, this electrochemical study highlights new features of ZnO-Fe-MXene for CO2 reduction.