Fluorine doped tin oxide coated glass slides were evaluated for their chemical stability in different pH solutions at room temperature by carrying out potentiodynamic polarization and cyclic voltammetry (CV). The FTO was more stable in 0.1 M HNO3 and 0.1 M NaCl solutions under both anodic and cathodic polarization conditions. Cathodic polarization in 0.1 M HCl solution resulted in a reduction of SnO2 to lower valent species. The semiconductivity of FTO, which was n-type at low anodic potentials, was p-type at high anodic potentials possibly due to the formation of a SnO-type surface layer by the removal of lattice oxygen during the oxygen evolution reaction. Cyclic stability of the FTO was evaluated by conducting CV between −2.0 and vbn 2.0 VAg/AgCl at 1 V/s. Intergranular corrosion was observed and the stability was completely lost after 215 cycles in the 0.1 M HCl solution. The stability of FTO was better in the 0.1 M NaOH solution, wherein the electro-catalytic activity degraded after 500 cycles, the electrical connectivity was maintained even after 4500 cycles.
Inconel 718 (UNS N07718) is a nickel-base superalloy containing iron that is used at cryogenic temperatures (arctic pipe components) and at high temperatures (gas turbines). This alloy is also used in off-shore oil drilling due to its high overall strength and resistance to corrosion. Inconel 718 components are created by a selective laser melting (SLM) additive manufacturing route and result in isotropic fine-grained microstructures with metastable phases (such as Laves phases) that are not usually present in conventional manufacturing processes. In this work, SLM Inconel 718 alloy specimens were investigated in four different conditions: (1) As-manufactured (AS-AM), (2) Additively manufactured and hot isostatically pressed (AM-HIP), (3) As-manufactured and heat-treated (solution annealing followed by two-step aging), and 4) AM-HIP and heat-treated. Localized corrosion behavior was evaluated at room temperature in a 3.5% NaCl solution at three different pH conditions (pH 1.25, 6.25, and 12.25). Electrochemical tests, including linear polarization, cyclic polarization, potentiostatic conditioning, electrochemical impedance spectroscopy, and Mott–Schottky analyses, were used to compare the corrosion behaviors of the SLM specimens with that of the conventionally wrought IN718 samples. The results showed that the additively manufactured specimens showed better corrosion resistance than the wrought material in the acidic chloride solution, and the AM-HIP specimens exhibited superior corrosion resistance to the as-manufactured ones. Hot isostatic pressing resulted in the visible elimination of the dendritic structure, indicating compositional homogeneity as well as a significant decrease in porosity. In addition, the deleterious secondary phases, such as Laves and δ phases, were not observed in the microstructure of the HIPed samples. The AM-HIP material showed the highest corrosion resistance in all the pH conditions. The two-step aging treatment, in general, resulted in the deterioration of corrosion resistance, which could be attributed to the formation of γ′ and γ″ precipitates that increased the cathodic reaction catalytic activities. In the additively manufactured samples, the presence of the Laves phase was more detrimental to corrosion resistance than any other phases and MC carbide and grain boundary δ phase increased the susceptibility to corrosion in wrought materials.
This study aims to construct a novel and sustainable approach for remediating aquaculture-generated water contamination using various engineered biochars. Particularly, this study focuses on capturing nitrogen and phosphorus from downstream water of commercial fish farms in Magic Valley, Idaho, containing approximately 2.26 mg/L of nitrogen and 0.15 mg/L of phosphorous. The results indicate that the proposed approach can improve downstream waters by adsorbing micronutrients (e.g., nitrogen-ammonia, nitrate-n + nitrite-n, and total phosphorus). Water treatment time and biochar pH are two key parameters strongly associated with adsorbed compounds. Molecular-level characterization of solvent-extracted organics from biochar materials (before and after water treatment) suggests increased levels of highly oxygenated molecules as a function of increasing water treatment time. Also, the results show the enrichment in organic species with higher molecular weight and increased double bond equivalents, with a compositional range similar to that of dissolved organic matter. Upon water treatment, extracted organics revealed higher abundances of compounds with higher H/C and O/C ratios. The engineered biochars, after water treatment, can be reused as nutrient-rich fertilizers. This study concluded that the engineered biochars could sequester more nitrogen and phosphorous over time. Also, the proposed approach can simultaneously increase fish production capacity and support the aquaculture industry in different regions by improving water quality and enabling aquaculture expansion.
Dry storage canisters of used nuclear fuels are fabricated using SUS 304L stainless steel. Chloride-induced stress corrosion cracking (CISCC) is one of the major failure modes of dry storage canisters. The cracked canisters can be repaired by friction stir welding (FSW), a low-heat input ‘solid-phase’ welding process. It is important to evaluate the ClSCC resistance of the friction stir welded material. Stress corrosion cracking (SCC) studies were carried out on mill-annealed base materials and friction stir welded 304L stainless U-bend specimens in 3.5% NaCl + 5 N H2SO4 solution at room temperature and boiling MgCl2 solution at 155 °C. The engineering stress on the outer fiber of the FSW U-bend specimen was ~60% higher than that of the base metal (BM). In spite of the higher stress level of the FSW, both materials (FSW and BM) showed almost similar SCC failure times in the two different test solutions. The SCC occurred in the thermo-mechanically affected zone (TMAZ) of the FSW specimens in the 3.5% NaCl + 5 N H2SO4 solution at room temperature, while the stirred zone (SZ) was relatively crack-free. The failure occurred at the stirred zone when tested in the boiling MgCl2 solution. Hydrogen reduction was the cathodic reaction in the boiling MgCl2 solution, which promoted hydrogen-assisted cracking of the heavily deformed stirred zone. The emergence of the slip step followed by passive film rupture and dissolution of the slip step could be the SCC events in the 3.5% NaCl + 5 N H2SO4 solution at room temperature. However, the slip step height was not sufficient to cause passivity breakdown in the fine-grained SZ. Therefore, the SCC occurred in the partially recrystallized softer TMAZ. Overall, the friction-stirred 304L showed higher tolerance to ClSCC than the 304L base metal.