Search Results (3)

Escalating environmental concerns have dictated the need to develop innovative methods for efficiently desulfurizing marine fuels (heavy fuel oils). In this work, the oxidative desulfurization method using deep eutectic solvents (DESs) was applied to reduce the sulfur content in a commercially available heavy fuel oil (HFO) below 0.5 wt.%, as current regulations demand. Initially, the S-compounds in the fuel were oxidized using an oxidative mixture of H₂O₂ with carboxylic acid (either acetic or formic acid). Subsequently, the oxidized S-compounds were extracted from the fuel using a series of environmentally friendly deep eutectic solvents (DESs), the best of which was proven to be a mixture of choline chloride with ethylene glycol at a 1/2 molar ratio. The process was optimized by investigating the effect of several process parameters on the desulfurization efficiency, namely, the H₂O₂/S molar ratio, the H₂O₂/acid molar ratio, the acid type, the oxidation temperature and oxidation time, the solvent/fuel mass ratio, the extraction time, and the extraction temperature. A desulfurization efficiency of 75.7% was achieved under the optimized conditions, reducing the S content in the fuel to 0.33 wt.%. Furthermore, different methods to recycle the DESs were investigated, and consecutive desulfurization and solvent regeneration cycles were performed. The most efficient recycling method was determined to be the anti-solvent addition of excess water, which resulted in 89.5% DES purification by causing precipitation of the dissolved solids. After three cycles of desulfurization and regeneration using different recycling routes, it was found that the regeneration degree declines gradually; however, it is more than 79.3% in all cases. Full article

The synthesis of YBa₂Cu₃O_7−x (YBCO or 123) was carried out via the use of a variety of deep eutectic solvents (DESs), all formed by the interaction of choline hydroxide (as the cation source) and alkyl carboxylic acids with C_nH_2n+1 ranging from n = 2 to n = 10, namely acetic acid, propionic acid, butyric acid, pentanoic acid, nonanoic acid, and decanoic acid, as providers of the anion, all prepared in equimolar solutions. The behaviour of the synthetic media and the resulting morphology displayed by the crystallite product, using different molar ratios of DESs (X):1 YBaCu metal nitrates mixes, with x values of 20 ≤ x ≤ 60, is also reported. Synthetic performance results show a tendency to generate higher total phase percentage of the desired crystal with the increase of the alkyl chain length of the carboxylic acid up to butyric acid (92% belonging to the metal oxide), after which no enhancement was observed. Furthermore, the synthetic performance of the remaining, i.e., DES formed with pentanoic acid to decanoic acid, displayed a constant decay in total desired phase percentage belonging to the metal oxide. Morphological results were also analysed for all DESs (X):1 YBaCu metal nitrates mixes, with x values of 20 ≤ x ≤ 60. Well defined plate-like particles were generally observed however, in some cases fused plate-like particles of significantly bigger size were observed. Full article

Four novel choline carboxylate aqueous solution systems were developed by mixing H₂O with choline nicotinate [Ch][Na], choline ferulate [Ch][Fa], choline vanillate [Ch][Va] and choline syringate [Ch][Sa]. The solubility of lignin in the four solvents was determined at 25 °C. The influence of the molar ratio of H₂O to [Ch][Na] ([Ch][Fa], [Ch][Va] and [Ch][Sa]) and the anionic structure on lignin solubility were systematically investigated. It was found that, the anionic structure and H₂O content significantly affected lignin dissolution. Interestingly, H₂O/[Ch][Na] and H₂O/[Ch][Fa] solvents show efficient capacity for lignin dissolution even at room temperatures. The dissolution of lignin in H₂O/[Ch][Na] and H₂O/[Ch][Fa] solvents is mainly ascribed to the interaction of lignin with the alkyl chain in the anion and cation dissociated from [Ch][Na]([Ch][Fa]) by H₂O. In addition, the recycling of the lignin solvent was examined, and the structure and thermostability of the lignin regenerated from the solvent were also estimated. Full article