Several biodiesel fuel samples produced from rapeseed oil by the noncatalyzed transesterification reaction with supercritical ethanol at various temperatures from (593 to 653) K and molar ethanol to rapeseed oil ratios from (6:1 to 20:1) were used to measure kinematic viscosity. Measurements were made using the capillary viscometer (VPZ-2, Labtex Com., Moscow). The combined expanded uncertainty of the kinematic viscosity measurements at the 95 % confidence level with a coverage factor of k = 2 is estimated to be 0.35 %. All measurements were made at temperature of 313.5 K (ASTM D445) and at atmospheric pressure. The effect of fatty acid ethyl esters (FAEEs) content on the kinematic viscosity of biodiesel fuel samples at 313.15 K was studied. The correlation between the FAEEs concentration in biodiesel fuel samples and their measured kinematic viscosity at 313.15 K was found. The derived correlation between the kinematic viscosity and the FAEEs contents allows controlling the progress of the rapeseed oil transesterification process with supercritical ethanol.
A quantum-chemical study of the mechanism of transesterification reaction carried out in the traditional and supercritical fluid (SCF) conditions has been performed. Samples of biodiesel fuel have been derived from rapeseed oil in the environment of supercritical ethanol using a flow type unit, both in the absence and in the presence of heterogeneous catalysts-metal oxides. Experimental studies of kinematic viscosity of a large array of samples of derived biodiesel have been performed. The viscous correlation allowing determining the content of the desired product-fatty acid ethyl esters (FAEE)-in biodiesel samples, has been made based on the obtained experimental data on the kinematic viscosity of biodiesel samples. The influence of change of the dielectric permittivity of working environments on the rate of reaction of transesterification in the supercritical fluid conditions has been revealed.
This work reports supercritical water oxidation (SCWO) of organic pollutants in industrial wastewater in the absence and presence of catalysts. To increase the efficiency of the oxidation process, the SCWO of organic compounds in industrial wastewater was performed in the presence of various iron- and manganese-containing heterogeneous catalysts (Fe-Ac, Fe-OH, and Mn-Al). The catalytic and non-catalytic SCWO of organic compounds in wastewater from PJSC “Nizhnekamskneftekhim”, generated from the epoxidation of propylene with ethylbenzene hydroperoxide in the process of producing propylene oxide and styrene (PO/SM), was performed. The effect of operational parameters (temperature, pressure, residence time, type of catalysts, oxygen excess ratio, etc.) on the efficiency of the process of oxidation of organic compounds in the wastewater was studied. SCWO was studied in a flow reactor with induction heating under different temperatures (between 673.15 and 873.15 K) and at a pressure of 22.5 MPa. The reaction time ranged from 1.8 to 4.83 minutes. Compressed air was used as an oxidizing agent (oxidant) with an oxidant ratio of two to four. A pseudo-first-order model expressed the kinetics of the SCWO processes, and the rate constants were evaluated. In the present work, in order to optimize the operation parameters of the SCWO process, we used the thermodynamic properties of near- and supercritical water by taking into account the asymmetric behavior of the liquid–vapor coexistence curve.
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