Apparent Kinetics of Co-Gasification of Biomass and Vacuum Gas Oil (VGO).

This communication reports the beneficial effects of co-gasification of biomass and residual oil to produce syngas. In this regard, various blends of glucose (a biomass surrogate) to vacuum gas oil (VGO) have been employed to investigate the synergic effects on the gasification process. The non-isothermal co-gasification experiments were conducted in a thermogravimetric analyzer at different heating rates and gasifying agents. The analysis showed that the co-gasification rate increased with the increase of glucose content in the feedstock. The presence of the oxygen in the biomass molecules helped the overall gasification process. The maximum gasification rate of 42.70 wt/min (DTGmax ) was observed with 25 wt% glucose containing sample. The use of gasifying agents appeared to have some influence, especially during high temperature gasification of the glucose-VGO blends. At a same gasification temperature, the co-gasification rate of glucose-VGO blends were found to be 125.7 wt/min and 98.59 wt%/min for N2 and CO2 , respectively. The kinetics of the co-gasification of glucose-VGO blends was conducted based on modified random pore model using TGA experimental data and implemented in MATLAB. The estimated activation energy and rate constants were found to be consistent to the observed co-gasification rates. The apparent activation energies of co-gasification of VGO/biomass blends with different weight percentages shows values ranging 60.56-48.25 kJ/mol. The kinetics analysis suggested that the addition of biomass helped to increase the reaction rate by lowering the activation energy required for accomplishing the reactions compared with petroleum carbonaceous feedstocks. The reaction rate constants isotherms are plotted to show that the k-values are exhibiting similar trends at moderate heating rates between 20 and 60 °C/min. This remark arises due to the nature of the reactions involved which are considered to be inherently similar in this range of heating rate.

Zr doping on one-dimensional titania nanomaterials synthesized in supercritical carbon dioxide.

The growth mechanism of one-dimensional metal oxide nanotubular structures is of tremendous current interest to tailor materials using "green" synthetic procedures for emerging industries in alternative energy and biomaterials. In this study, ZrO(2)-modified TiO(2) nanorods and tubular structures were successfully synthesized via a surfactant-free sol-gel route using supercritical carbon dioxide (scCO(2)) as the solvent/drying agent. The effect of metal alkoxide concentration (0.35-1.4 mol/L), acid/metal alkoxide ratio (R = 3-7), and Zr ratio (0-20%) was examined on the morphology and crystallinity of the resulting nanostructures as measured by electron microscopy (SEM and TEM), EDX, XPS, and XRD. The electron microscopy results showed that the crystal growth of the synthesized binary Ti-Zr nanomaterials could be tailored by changing the operating variables with nanotubular structure formed at metal alkoxide concentration of 1.2 mol/L, R = 5-6, and Zr ratio between 4% and 20%. Gelation kinetics for this new system was also studied and revealed that increasing alkoxide concentration and R value enhanced the gelation kinetics. In situ and powder FTIR results revealed that this Ti-Zr binary system follows a similar reaction scheme to that of either single-component system, showing the flexibility of this approach for tailoring nanotubular production.

One-pot procedure to synthesize high surface area alumina nanofibers using supercritical carbon dioxide.

For the first time, high surface area nanofibers were synthesized using aluminum isopropoxide monomer with acetic acid as the polycondensation agent in the green solvent, supercritical carbon dioxide (scCO(2)). It was found that the synthesis temperature, pressure, concentration, and acid/alkoxide ratio had a large effect on fiber formation. By optimizing the experimental conditions at 80 degrees C and 6000 psi of scCO(2) using aluminum isopropoxide at a concentration of 0.3 mmol/mL and acid/alkoxide ratio of 10, alumina nanofibers were formed ranging from 11 to 22 nm in diameter and 500 to 1000 nm in length, and with surface areas up to 580 m(2)/g. Lower temperatures gave irregular shaped nanoparticles, while a lower acid/alkoxide ratio (5:1) resulted in the formation of low surface area alumina bars. Increasing pressure led to better separation of the nanofibers and higher surface areas. In addition to the synthesis conditions, the influence of calcination temperature on the structural, textural, and morphological properties of the materials was examined using various physicochemical techniques including electron microscopy, TGA/DTA, powder XRD, FTIR, XPS, and nitrogen adsorption/desorption analysis. The long fibers with high aspect ratios were found to be thermally stable even after calcining at up to 1050 degrees C. The mechanism of fiber formation in scCO(2) is proposed based on a [Al(OH)(CH(3)CO(2))(2)](n) polycondensate backbone.

Study of the RESS process for producing beclomethasone-17,21-dipropionate particles suitable for pulmonary delivery.

The purpose of this research was to micronize beclomethasone-17,21-dipropionate (BDP), an anti-inflammatory inhaled corticosteroid commonly used to treat asthma, using the rapid expansion of supercritical solution (RESS) technique. The RESS technique was chosen for its ability to produce both micron particles of high purity for inhalation, and submicron/nano particles as a powder handling aid for use in next generation dry powder inhalers (DPIs). Particle formation experiments were carried out with a capillary RESS system to determine the effect of experimental conditions on the particle size distribution (PSD). The results indicated that the RESS process conditions strongly influenced the particle size and morphology; with the BDP mean particle size decreasing to sub-micron and nanometer dimensions. An increase in the following parameters, i.e. nozzle diameter, BDP mol fraction, system pressure, and system temperature; led to larger particle sizes. Aerodynamic diameters were estimated from the SEM data using three separate relations, which showed that the RESS technique is promising to produce particles suitable for pulmonary delivery.