The influence of pyrolysis type on shale oil generation and its composition (Upper layer of Aleksinac oil shale, Serbia)

The influence of pyrolysis type on shale oil generation and its composition was studied. Different methods such as Rock-Eval pyrolysis, thermogravimetric analysis (TGA) and pyrolysis in the open and closed systems were applied. Samples from the Upper layer of Aleksinac oil shale (Serbia) were used as a substrate and first time characterized in detail. The impact of kerogen content and type on the shale oil generation in different pyrolysis systems was also estimated. Majority of the analysed samples have total organic carbon content > 5 wt. % and contain oil prone kerogen types I and/or II. Therefore, they can be of particular interest for the pyrolytic processing. Thermal behavior of analysed samples obtained by TGA is in agreement with Rock-Eval parameters. Pyrolysis of oil shale in the open system gives higher yield of shale oil than pyrolysis in the closed system. The yield of hydrocarbons (HCs) in shale oil produced by open pyrolysis system corresponds to an excellent source rock potential, while HCs yield from the closed system indicates a very good source rock potential. The kerogen content has a greater impact on the shale oil generation than kerogen type in the open pyrolysis system, while kerogen type plays a more important role on generation of shale oil than the kerogen content in the closed system. The composition of obtained shale oil showed certain undesirable features, due to the relatively high contents of olefinic HCs (open system) and polar compounds (closed system), which may require further treatment to be used

Моделирование кинетики прямого амидирования жирных кислот диэтаноламином

BACKGROUND: , Aims and Scope. In oil spill investigations, one of the most important steps is a proper choice of approaches that imply an investigation of samples taken from different sedimentary environments, samples of oil contaminants taken in different periods of time and samples taken at different distances from the oil spill. In all these cases, conclusion on the influence of the environment, microorganisms or migration on the oil contaminants' composition can be drawn from the comparison of chemical compositions of the investigated contaminants. However, in case of water contaminants, it is very important to define which part of organic matter has been analyzed. Namely, previous investigations showed that there were some differences in chemical composition of the same oil contaminant depending on the intensity of its contact with ground water. The aim of this work is to define more precisely the interactions between oil contaminant and water, i.e. the influence of the intensity of interaction between the oil contaminant and water on its chemical composition. The study was based on a comparison of four fractionated extracts of an oil pollutant, after they had been analyzed in details. Methods. Oil polluted surface water (wastewater canal, Pancevo, Serbia) was investigated. The study was based on a comparison of four extracts of an oil contaminant: extract I (decanted part), and extracts 2, 3 and 4 (extracted by shaking for 1 minute, 5 minutes and 24 hours, respectively). The fractionated extracts were saponified with a solution of KOH in methanol, and neutralized with 10% hydrochloric acid. The products were dissolved in a mixture of dichloromethane and hexane, and individually fractionated by column chromatography on alumina and silica gel (saturated hydrocarbon, aromatic, alcohol and fatty acid fractions). n-Alkanes and isoprenoid aliphatic alkanes, polycyclic alkanes of sterane and triterpane types, alcohols and fatty acids were analyzed using gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). delta C-13(PDB) values of individual n-alkanes in the aliphatic fractions were determined using gas chromatography-isotope ratio monitoring-mass spectrometry (GC-irmMS). Results and discussion. Extracts 1 and 2 are characterized by uniform distribution of n-alkanes, whereas extract 3 is characterized by an even-numbered members dominating the odd-ones, and extract 4 showed a bimodal distribution. Extract I is characterized by the least negative delta C-13(PDB) values of C-19-C-26 n-alkanes. Sterane and triterpane analysis confirmed that all extracts originated from the same oil contaminant. n-Fatty acids, C-19-C-24, in all extracts are very low, being somewhat higher in extract 4. Even-numbered n-alcohols, C-12-C-16, were identified in the highest concentration in extract 3. It was assumed that algae were responsible for the composition of extract 3. Furthermore, a possible reason for higher concentrations of C-19-C-26 n-alkanes and C-19-C-24 fatty acids in extract 4 is the formation of inclusion compounds with colloidal micelles formed between the oil contaminant's NSO-compounds and water. Conclusion. It was undoubtedly confirmed that there were specific differences in the compositions of the different extracts depending on the intensity of the interaction between the oil contaminant and the surface water. Recommendation and Outlook. When comparing the composition of oil contaminants from different water samples (regardless of the ultimate investigation goal) it is necessary to compare the extracts isolated under the same conditions, in other words, extracts that were in the same or very similar interaction with water. Recommendation and Outlook. When comparing the composition of oil contaminants from different water samples (regardless of the ultimate investigation goal) it is necessary to compare the extracts isolated under the same conditions, in other words, extracts that were in the same or very similar interaction with water

The IR Spectra, Molar Absorptivity, and Integrated Molar Absorptivity of the C76-D2 and C84-D2:22 Isomers

The FT-IR spectra of the stable C76 and C84 isomers of D2 symmetry, isolated by the new, advanced extraction and chromatographic methods and processes, were recorded by the KBr technique, over the relevant region from 400 to 2000 cm−1, at room temperature. All the observed infrared bands are in excellent agreement with the semiempirical QCFF/PI, DFT, and TB potential calculations for these fullerenes, which is presented in this article, as the evidence of their validity. The molar absorptivity ε and the integrated molar absorptivity ψ of their IR absorption bands were determined and reported together with the relative intensities. Excellent agreement is found between the relative intensities of the main and characteristic absorption maxima calculated from ελ and from the ψλ values in adequate integration ranges. These results are significant for the identification and quantitative determination of the C76-D2 and C84-D2:22 fullerenes, either in natural resources on Earth and in space or in artificially synthesized biomaterials, electronic, optical, and biomedical devices, sensors, polymers, optical limiters, solar cells, organic field effect transistors, special lenses, diagnostic and therapeutic agents, pharmaceutical substances in biomedical engineering, and so forth