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The objective of this work was to synthesize cellulose acetate from sorghum bagasse, a promising raw material for the production of chemical inputs, both from a photosynthetic point of view and the maturation speed compared with that of sugarcane. The bagasse was treated with hydrogen peroxide, and then cellulose was isolated using sodium chlorite, acetic acid, and sodium hydroxide. The cellulose was subjected to an acetylation reaction, from which cellulose triacetate was obtained. By means of statistical analysis, it was observed that the conditions that generated the highest solubilization of lignin (62%) and higher yield from cellulose extraction (39.5%) were 60 °C, a 6% peroxide concentration, and 4 h. Cellulose acetate was obtained with a degree of substitution of 3.66 at 25 °C and 24 h. Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetry, differential thermogravimetry, and differential scanning calorimetry analyses confirmed that the obtained cellulose presented specific characteristics of this material. Also, the reaction of acetylation was confirmed through these techniques. [ABSTRACT FROM AUTHOR]

The objective of this work has been the synthesis of wollastonite by solution combustion method. The novelty of this work has been obtaining the crystalline phase without the need of thermal treatments after the synthesis. For this purpose, urea was used as fuel. Calcium nitrate was selected as a source of calcium and colloidal silica served as a source of silicon. The effect of the amount of fuel on the combustion process was investigated. Temperature of the combustion reaction was followed by digital pyrometry. The obtained products were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and specific surface area. The results showed that the combustion synthesis provides nanostructured powders characterized by a high surface area. When excess of urea was used, wollastonite-2M was obtained with a submicronic structure. [ABSTRACT FROM AUTHOR]

Abstract: Pt–Rare Earth/C electrocatalysts (Rare Earth=La, Ce, Pr, Nd, Sm, Tb, Dy, Ho and Er) were prepared by an alcohol reduction process using ethylene glycol as reduction agent and solvent and Vulcan XC72 as support. The electrocatalysts were characterized by energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electro-oxidation of methanol was studied in acid medium by cyclic voltammetry and chronoamperometry using thin porous coating technique. The XRD patterns indicate that all electrocatalysts present the face-centered cubic (fcc) structure of Pt and the presence of Rare Earth hydroxides. PtEr/C, PtTb/C, PtLa/C, PtDy/C and PtNd/C electrocatalysts prepared by this methodology showed superior performance for methanol electro-oxidation at room temperature compared to Pt/C. [Copyright &y& Elsevier]