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This study aimed to improve the production of biodiesel from white palm larvae (WPL) and to evaluate its potential as a feedstock. The larvae were grown using kitchen and palm waste for 21 days, and the crude oil was then extracted. The extracted oil was analyzed for its physicochemical properties and fatty acid composition. The analysis found that the feedstock oil contained a high quantity of monounsaturated fatty acids, indicating its suitability for biodiesel production. To optimize the production process, response surface methodology (RSM) was employed. A central composite design was used to study four operating conditions: temperature, methanol‐to‐oil mole ratio, esterification time, and catalyst loading for esterification, as well as transesterification time and catalyst concentration. The best conditions for esterification were a methanol‐to‐oil ratio of 18:1, a temperature of 70 °C, 120 min of reaction time, and a 4% H2SO4 catalyst. For transesterification, the optimal conditions were a methanol‐to‐oil ratio of 10:1, a temperature of 65 °C, 90 min of reaction time, and a 2% KOH catalyst concentration. The experimental data fit well with models, with significant P‐values and high R2 values. The biodiesel produced under the optimized conditions met the fuel quality standards set by Brazilian, European, and American standards. In conclusion, this study successfully optimized the biodiesel production process from white palm larvae and confirmed its suitability as a feedstock. The feedstock oil had properties that were suitable for biodiesel production, and the optimized conditions resulted in biodiesel that met fuel‐quality standards. [ABSTRACT FROM AUTHOR]

The present study aimed at characterizing the oil extracted from Bertholletia excelsa H.B.K. almond, a native species from the Amazon region. Analytical methods used for oils and fats were employed through pharmacopoeia assays, AOCS (American Oil Chemists Society) standard methods as well as those recommended by ANVISA (National Health Surveillance Agency) such as acidity, peroxide value, saponification index, iodine value and refractive index, pH and relative density, and also thermoanalytical analyses (thermogravimetry, differential thermogravimetry and differential thermal analysis) as well as chromatographic analysis (gas chromatography). The characterization assessments of B. excelsa oil showed results indicating that the oil contains polyunsaturated fatty acids in large proportion. The termoanalytical tests indicated that B.excelsa oil showed thermal stability up to 220 °C, These results showed that the oil extracted from B. excelsa has acceptable characteristics and is of good quality. [ABSTRACT FROM AUTHOR]

The interaction of copaiba oil in the polymer matrix of chitosan can produce a favorable synergistic effect and potentiate properties. Indeed, the bioactive principles present in copaiba oil have anti-inflammatory and healing action. In the present work, chitosan membranes containing different contents of copaiba oil copaíba (0.1, 0.5, 1.0 and 5.0% (v/v)) were for the first time investigated. The membranes were developed by the casting method and analyzed for their morphology, degree of intumescence, moisture content, contact angle, Scanning Electron Microscope, and X-ray diffractometry. These chitosan/copaiba oil porous membranes disclosed fluid absorption capacity, hydrophilic surface, and moisture. In addition, the results showed that chitosan membranes with the addition of 1.0% (v/v) of copaiba oil presented oil drops with larger diameters, around 123.78 μm. The highest fluid absorption indexes were observed in chitosan membranes containing 0.1 and 0.5% (v/v) of copaiba oil. In addition, the copaiba oil modified the crystalline structure of chitosan. Such characteristics are expected to favor wound treatment. However, biological studies are necessary for the safe use of chitosan/copaiba oil membrane as a biomaterial. [ABSTRACT FROM AUTHOR]

In this work, a new morphology was obtained for bismuth tungstate (Bi2WO6-glyc) using a hydrothermal method with the addition of glycerol as a surfactant. In order to compare, the bismuth tungstate without glycerol as the surfactant, i.e., Bi2WO6, was synthesized. Structural characterization by XRD and Rietveld refinement confirmed the orthorhombic structure as a single phase for all samples with high crystallinity. All active modes in Raman spectroscopy for the orthorhombic phase of bismuth tungstate were confirmed in agreement with XRD analysis. N2 adsorption/desorption and size pore distribution confirmed the high surface area (85.7 m2/g) for Bi2WO6-glyc when compared with Bi2WO6 (8.5 m2/g). The optical band gap by diffuse reflectance was 2.78 eV and 2.88 eV for Bi2WO6-glyc and Bi2WO6, respectively. SEM images confirmed the different morphology for these materials, and microstructures with cheese crisp were observed for Bi2WO6-glyc (cheese crisp). On the other hand, flower-like microcrystals were confirmed for Bi2WO6 sample. The photocatalytic performance of Bi2WO6-glyc (94.2%) in the photodegradation of rhodamine B (RhB) dye solutions at 60 min was more expressive than Bi2WO6 (81.3%) and photolysis (8.2%) at 90 min. [ABSTRACT FROM AUTHOR]

Production of alternative fuels, such as biodiesel, from transesterification of vegetable oil driven by heterogeneous catalysts is a promising alternative to fossil diesel. However, achieving a successful substitution for a new renewable fuel depends on several quality parameters. (1)H NMR spectroscopy was used to determine the amount of methyl esters, free glycerin and acid number in the transesterification of soybean oil with methanol in the presence of hydrotalcite-type catalyst to produce biodiesel. Reaction parameters, such as temperature and time, were used to evaluate soybean oil methyl esters rate conversion. Temperatures of 100 to 180 °C and times of 20 to 240 min were tested on a 1 : 12 molar ratio soybean oil/methanol reaction. At 180 °C/240 min conditions, a rate of 94.5 wt% of methyl esters was obtained, where free glycerin and free fatty acids were not detected., (Copyright © 2012 John Wiley & Sons, Ltd.)