Effects of Water Removal from Palm Oil Reactant by Electrolysis on the Fuel Properties of Biodiesel

Biodiesel, which is composed of mono-alkyl esters of long carbon-chained fatty acids, is used as an alternative fuel to petro-diesel. The water content of the reactant mixture of feedstock oil influences the extent of transesterification and thus the fuel characteristics. Lower water content in feedstock oil is generally suggested for successful transesterification. This experimental study removed water from the reactant mixture of feedstock palm oil and methanol during transesterification using various systems composed of either electrodes or molecular sieves with rotary vibration. The effect of input electrical energy, number of electrodes, vibration modes, and operating time on the amount of water removed from the reactant mixture and the fuel properties of the final biodiesel product were analyzed and compared with those achieved using molecular sieves. The results show that the biodiesel—after water was removed during transesterification—appeared to have increased kinematic viscosity, cetane index, distillation temperature, and acid value, while the heating value, flash point, ignition point, and water content decreased with an increase in the input electrical energy of the electrodes responsible for electrolyzing water away. Electrolysis by the double-pair electrodes was more effective at reducing acid value and water content than that performed by the single-pair electrodes under the same input electrical energy. The biodiesel was found to have the lowest water content (0.0304 wt.%) and the highest water-removal rate (0.011 wt.%) when water was removed during transesterification by the double-pair electrodes with an input electrical energy of 9 J/(g palm oil). The water-removal rate of the rotary-vibrating molecular sieves was 11.24 times that of the single-pair electrodes. The biodiesel was found to have increased kinematic viscosity with higher input electrical energy, reaching 5.15 mm2/s when the double-pair electrodes with an input electrical energy of 11 J/(g palm oil) were used. Longer carbon-chained fatty acids, ranging from C20 to C24, amounted to 0.74 wt.% of the biodiesel produced using the double-pair electrodes, which was greater than that seen for the single-pair electrodes. However, the molecular sieve method consumed more energy than the double-pair electrodes did to remove the same amount of water from the palm oil reactant mixture via transesterification.

Алгоритм предварительного анализа дифракционных спектров для нанокомпозитных материалов с примесью массивной фракции

This contribution is devoted to discussion of questions related to the influence of a possible contribution from a bulk material on the lineshape of elastic peaks observed in diffraction experiments at neutron and / or X-ray radiation scattering on nanoporous matrices containing substances embedded into their porous space (channels). The proposed algorithm permits to estimate the input of massive component into diffraction peaks using the analysis of the experimentally observed distortions of the lineshape of the Bragg peaks. This preliminary analysis greatly simplifies the profile analysis of nanocomposite diffraction patterns, especially for molecular sieves based on powders of SBA-15, MCM-41, MCM-48, etc. types.

Features of the Gas-Permeable Crystalline Phase of Poly-2,6-Dimethylphenylene Oxide

Poly-2,6-dimethylphenylene oxide (PPO) film samples with varying degrees of crystallinity (from 0 to 69%) were obtained by means of different techniques. The films were studied by various physicochemical methods (Fourier-transform infrared spectroscopy, positron annihilation lifetime spectroscopy, X-ray diffraction, and 1H nuclear magnetic resonance relaxation). Solubility coefficients of gases in the PPO samples were measured via sorption isotherms of gases by volumetric technique with chromatographic detection. The apparent activation energy of permeation and the activation energy of diffusion of all gases were estimated based on temperature dependences of gas permeability and diffusivity for amorphous and semi-crystalline PPO in the range of 20–50 °C. The peculiarities of free volume, density, and thermal properties of gas transport confirm the nanoporosity of the gas-permeable crystalline phase of PPO. So, the PPO can be included in the group of organic molecular sieves.

Investigating the properties and performance of 3A molecular sieves as an adsorbent to prevent coke formation in olefin dehydration process

To study the affinity of 3A aluminosilicate adsorbents to prevent oligomerization of olefin molecules and forming green oil, physical and chemical properties of 3A molecular sieves are measured by using characterization techniques such as temperature-programmed desorption (TPD), nitrogen (N2) and water adsorptions, X-ray diffraction (XRD), X-ray fluorescence (XRF), crushing strength, and carbon dioxide (CO2) adsorption. Moreover, coke formation affinities of the understudy adsorbents are evaluated in a bench-scale system using 1-butene and 1,3-butadiene at temperatures of 220 and 260 °C, and outcomes are validated against the actual data gathered from an industrial scale olefin dehydration plant. Results confirm that the type of binder and the amount of ion exchange affect the performance of a 3A molecular sieve nominated for dehydrating olefinic streams. The binder with the least amount of acidity is preferred, and at least 35% of Na ions of the 4A zeolite should be exchanged with K ions to make it applicable for synthesizing an appropriate 3A molecular sieve. Furthermore, to control the oligomerization and inhibit green oil formation, the CO2 adsorption and acidity of Trisiv shape molecular sieves with the sizes of 1/4 inch should be less than 0.5 wt % and 1.7 mmol NH3/g, respectively. For extrudate shape with the sizes of 1/16 inch CO2 adsorption and acidity should be less than 0.2 wt % and 2.2 mmol NH3/g, respectively.

Preparation, characterization and evaluation of x-MoO3/Al-SBA-15 catalysts for biodiesel production

Biodiesel is an alternative source of renewable energy that can be produced by a transesterification of vegetable oils. Mesoporous molecular sieves, such as SBA-15, due to high surface area and thermal stability are promising precursors for heterogeneous catalysts in the transesterification reaction. In this work, Al-SBA-15 precursor was obtained by direct hydrothermal synthesis, impregnated with different MoO3 contents (5, 10 and 15 wt%) by the pore saturation method, and evaluated as heterogeneous catalyst in the production of biodiesel from a transesterification of soybean oil with methanol. Al-SBA-15 precursor as well as MoO3/Al-SBA-15 catalyst were characterized for its structural characteristic by X-ray diffraction, textural characteristic by N2 adsorption analysis, and thermal stability by thermogravimetric analysis. An experimental planning 22 + 3 CtPt was used to evaluate the influence of MoO3 content and reaction time on biodiesel yield from soybean oil and methanol. The biodiesel content in the final product was obtained by gas chromatography. An average biodiesel yield of 96% was obtained with the catalyst 10%MoO3/Al-SBA-15 under the following reaction conditions: 20:1 methanol/soybean oil molar ratio, and 3 wt% of catalyst loading at 150 °C in 3 h. After five consecutive reaction cycles, the biodiesel yield decreased by about 34%. The density and acidity of the biodiesel produced are within the specified values for commercialization according to international standards. Graphical abstract