Chemical composition of different morphological parts from ‘Dwarf Cavendish’ banana plant and their potential as a non-wood renewable source of natural products

The study on chemical composition and structure of components from different morphological parts of ‘Dwarf Cavendish’ banana plant (petioles/midrib, leaf blades, floral stalk, leaf sheaths and rachis) have been carried out aiming to evaluate their potential as eventual raw materials for the chemical processing. Macromolecular components were analysed using solid-state NMR, ATR-FTIR and wet chemistry methods. Mineral components were assessed by ICP analysis of ashes obtained after raw material calcinations. It was verified that chemical composition of the studied fractions of banana plant varies significantly. The major extremes were found in the contents of cellulose (37.3% in leaf sheaths and only 15.7% in floral stalk), starch (26.3 in floral stalk and 0.4% in petioles/midrib), lignin (24.3% in leaf blades and 10.5% in rachis) and lipophilic extractives (5.8% in leaf blades and 1.2% in petioles/midrib). All morphologic parts of banana plant contained considerable amounts of ashes (from 11.6 to 26.8%) composed mainly by potassium, calcium and silicium salts. The hemicelluloses in banana plant are proposed to be mainly glucuronoxylan and xyloglucan (from 5.5% in floral stalk to 21.5% in petioles/midrib). Rather significant amount of proteins was found in leaf blades (8.3%). Lignin analysis revealed that it is of HGS type with H:G:S proportion ranged of (5–17):(18–54):(35–71). The significant variation of lignin structure among the different morphological parts of banana plant was highlighted. Results of this study allowed some propositions about possible applications of banana plant residues as non-wood renewable source of natural products.info:eu-repo/semantics/publishedVersio

Catalytic oxidation of formaldehyde by ruthenium multisubstituted tungstosilicic polyoxometalate supported on cellulose/silica hybrid

Cellulose/silica hybrid material produced by a sol–gel method from cellulosic fibres and silica precursors (tetraethoxysilane and 3-aminopropyltriethoxysilane) was functionalized with α-[SiW9O37RuIII3(H2O)xCl3−x](10−x)− (Ru-POM), and thoroughly characterised by 13C and 29Si solid state NMR, FTIR spectroscopy, UV–vis reflectance spectroscopy, X-ray diffraction, thermogravimetric analysis, scanning electron microscopy (SEM), and chemical analysis. The supported Ru-POM exhibited catalytic activity for the gas phase heterogeneous aerobic oxidation of formaldehyde (ca. 830 ppm in polluted air) at room temperature, in a packed-bed reactor operating at a linear velocity ca. 0.33 m/s and ca. 0.5 s residence time. Maximum formaldehyde uptake was 1.10 g/min per kg of hybrid material doped with Ru-POM (ca. 1.4% w/w). More than 400 turnovers were achieved without significant loss of catalytic activity and the only detected oxidation products of formaldehyde were carbon dioxide and water. A plausible mechanism for the catalytic oxidation of formaldehyde by supported Ru-POM has been proposed and includes formaldehyde oxidation in oxygenated ruthenium complex

Thermophysical characterization of ionic liquids able to dissolve biomass

Among new potential solvents for lignocellulosic materials, ionic liquids (ILs) are attracting considerable attention. Hence, the knowledge of the thermophysical properties of such fluids is essential for the design of related industrial processes. Therefore, in this work, a set of thermophysical properties, namely, density, viscosity, and refractive index, as a function of temperature, and isobaric thermal expansivity and heat capacities at a constant temperature, were determined for eight ionic liquids with the 1-ethyl-3-methylimidazolium cation combined with the following anions: acetate, methylphosphonate, methanesulfonate, trifluoromethanesulfonate, dicyanamide, thiocyanate, tosylate, and dimethylphosphate. Imidazolium-based ILs were chosen since these are the most studied ionic fluids in biomass dissolution approaches, while a large array of anions was investigated because it was already demonstrated that it is the IL anion that mainly governs the dissolution