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In this study, we tested several amino acids as eco-friendly inhibitors against corrosion of mild steel by used cooking oils (UCOs). The corrosion inhibition was studied by immersing mild steel rods in the UCOs and reference fresh rapeseed and olive oils mixed with amino acids. The immersion tests were conducted at room temperature for three days. The roles of water and bio-oil preservatives (formic and propionic acids) in the corrosion were explored. The mild steel surface morphology changes after exposure to the oils were analyzed with a scanning electron microscope coupled with an energy dispersive spectroscope (SEM-EDS). The concentration of iron dissolved in the oils was determined with a spectrophotometer. A thick layer was analyzed on the surfaces of the mild steel rods immersed in the oils containing formic or propionic acid and water. This layer provided a minor barrier against corrosion. According to the Fourier transform infrared spectrometer (FTIR) analytical results, the layer consisted of an acid and iron salt mixture. All the tested amino acids decreased the concentration of dissolved iron in the UCOs; particularly, cationic amino acids, L-lycine and L-arginine showed adequate corrosion inhibition properties at low concentrations. [ABSTRACT FROM AUTHOR]

Used cooking oils (UCOs) have a high potential as renewable fuels for the maritime shipping industry. However, their corrosiveness during storage and usage are some of the concerns yet to be investigated for addressing compatibility issues. Thus, the corrosion of steels and copper exposed to the UCOs was studied through the immersion of metal rods for different periods. The changes on the rod surfaces were analyzed with a scanning electron microscope (SEM). After the immersion, the copper concentration dissolved in the bio-oils was measured using inductively coupled plasma-optical emission spectrometry (ICP-OES). The free fatty acids and glycerides were analyzed using gas chromatography with flame ionization detection (GC-FID). The acid number (AN), water concentration, as well as density and kinematic viscosity of the bio-oils were determined with standard methods. The UCOs with the highest water content were corrosive, while the oils with lower water concentrations but higher ANs induced lower corrosion. After mixing two different UCOs, the metal corrosion decreased with an increasing concentration of the oil with lower corrosive properties. The lower corrosion properties were most likely due to the monounsaturated fatty acids, e.g., oleic acid in oils. These acids formed a barrier layer on the rod surfaces, thereby inhibiting the permeation of oxygen and water to the surface. Even adding 0.025 wt% of tert-butylamine decreased the corrosivity of UCO against polished steel rod. The results suggested that mixing several oil batches and adding a suitable inhibitor reduces the potential corrosive properties of UCOs. [ABSTRACT FROM AUTHOR]

Waste fish oils (FOs) and used cooking vegetable oils (UCOs) are increasingly becoming alternative renewable fuels. However, different physicochemical aspects of these renewable fuels, including the effect of storage, are not well-known. In this work, the effect of the storage period on physicochemical properties of selected samples of FOs and UCOs was investigated. The bio-oils were stored at 4 °C for up to five years before each experimentation. The chemical properties were characterized using capillary gas chromatography with flame ionization detection (GC-FID) and high-performance size exclusion chromatography including an evaporative light scattering detector (HPSEC-ELSD). Water contents and acid numbers of the bio-oils were determined using the Karl Fischer (KF) titration and the ASTM D 664 methods. Furthermore, the average heating values and surface tension of the bio-oils were determined. According to the results obtained, for all bio-oil types, the concentrations of polymerized triglycerides, diglycerides, and fatty acids and monoglycerides had increased during the storage periods. The physical properties of the bio-oils also showed a small variation as a function of the storage period. The overall results observed indicate that the deterioration of the physicochemical properties of bio-oils can be controlled through storage in dark, dry, and cold conditions. [ABSTRACT FROM AUTHOR]

Hazelnut (HS) and walnut (WS) shells, an abundant by-product of the processing industries of these edible nuts, are traditionally considered as a low-value waste. However, they are a source of valuable compounds with an interesting chemical profile for the chemical and pharmaceutical sectors. In this study, the lipophilic and hydrophilic extracts present in HS and WS were quantified and identified, then the polar fractions were chromatographically separated, and their antioxidant capacity was studied. The experimental work includes the isolation of crude lipophilic and hydrophilic extracts by an accelerated extraction process, chromatographic analysis (gas chromatography-flame ionization (GC-FID), GC-mass spectroscopy (GC-MS), high-performance size-exclusion chromatography (HPSEC), thin-layer chromatography (TLC)), and quantification of the components. In addition, a thorough compositional characterization of the subgroups obtained by flash chromatography and their antioxidant capacity was carried out. The gravimetric concentrations showed different lipophilic/hydrophilic ratios (0.70 for HS and 0.23 for WS), indicating a higher proportion of polar compounds in WS than in HS. Moreover, the lipophilic extracts were principally composed of short-chain fatty acids (stearic, palmitic, and oleic acid), triglycerides, and sterols. The polar fractions were screened by thin-layer chromatography and then separated by flash chromatography, obtaining fractions free of fatty acids and sugar derivatives (97:3 in HS and 95:5 in WS), and mixtures richer in phenolic compounds and flavonoids such as guaiacyl derivatives, quercetin, pinobanksin, and catechin. The most polar fractions presented a higher antioxidant capacity than that of the crude extracts. [ABSTRACT FROM AUTHOR]

The corrosion behavior of three used cooking oils and one non-edible fish oil was experimentally investigated by the immersion test of iron rods at room temperature. The corrosivity of the tested oils was indirectly determined from the amount of the dissolved iron in the tested oils after the immersion test. Different factors that affect the corrosive behavior of the tested oils were assessed. Among the tested oils, the fish oil showed the highest amount of dissolved iron owing to its chemical properties such as high water content and acid number. In general, water content and acid number have direct effects on the amount of dissolved iron. The addition of oleic acid to the used cooking oil resulted in a 60% less amount of dissolved iron. It was suggested that the addition of oleic acid prompted the formation of a monolayer, which inhibited the permeation of oxygen and water to the surface of the iron rod. Moreover, the addition of glycerol gave the lowest amount of dissolved iron in the oil sample owing to its ability to bind water molecules and form microemulsions in the presence of a surfactant (for example, oleic acid). [ABSTRACT FROM AUTHOR]