Browsing by Keyword "Biomass"
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Item Determination of Hemicellulose, Cellulose, and Lignin Content in Different Types of Biomasses by Thermogravimetric Analysis and Pseudocomponent Kinetic Model (TGA-PKM Method)(2020-09) Díez, David; Urueña, Ana; Piñero, Raúl; Barrio, Aitor; Tamminen, Tarja; BIOECONOMÍA Y CO2The standard method for determining the biomass composition, in terms of main lignocellulosic fraction (hemicellulose, cellulose and lignin) contents, is by chemical method; however, it is a slow and expensive methodology, which requires complex techniques and the use of multiple chemical reagents. The main objective of this article is to provide a new efficient, low-cost and fast method for the determination of the main lignocellulosic fraction contents of different types of biomasses from agricultural by-products to softwoods and hardwoods. The method is based on applying deconvolution techniques on the derivative thermogravimetric (DTG) pyrolysis curves obtained by thermogravimetric analysis (TGA) through a kinetic approach based on a pseudocomponent kinetic model (PKM). As a result, the new method (TGA-PKM) provides additional information regarding the ease of carrying out their degradation in comparison with other biomasses. The results obtained show a good agreement between experimental data from analytical procedures and the TGA-PKM method (±7%). This indicates that the TGA-PKM method can be used to have a good estimation of the content of the main lignocellulosic fractions without the need to carry out complex extraction and purification chemical treatments. In addition, the good quality of the fit obtained between the model and experimental DTG curves (R2Adj = 0.99) allows to obtain the characteristic kinetic parameters of each fraction.Item Electrosynthesis of 2,3-butanediol and methyl ethyl ketone from acetoin in flow cells(2019) Ochoa-Gómez, José R.; Fernández-Carretero, Francisco; Río-Pérez, Francisca; García-Luis, Alberto; Roncal, Tomás; García-Suárez, Eduardo J.; Tecnalia Research & Innovation; TECNOLOGÍAS DE HIDRÓGENO; BIOECONOMÍA Y CO2Acetoin could shortly become a platform molecule due to current progress in fermentation technology, the megatrend for shifting from an oil-based economy to one based on biomass, the quest for green manufacturing processes and its two highly reactive carbonyl and hydroxyl moieties. In this paper, the successful electro-conversion of acetoin into two valuable chemicals, 2,3-butandiol (2,3-BD) and methyl ethyl ketone (MEK), at constant electrical current in aqueous phase at room temperature using both divided and undivided 20 cm2 filter-press flow cells under experimental conditions suitable for industrial production is reported. Cathode material is the key parameter to drive the electroreduction towards one or another chemical. 2,3-BD is the major chemical produced by electrohydrogenation when low hydrogen overvoltage cathodes, such as Pt and Ni, of high surface area obtained by PVD coating on a carbon gas diffusion layer are used, while MEK is the principal product produced by electrohydrogenolysis when high hydrogen overvoltage cathodes, such as graphite, Pb and Cd foils, are employed. 2,3-BD and MEK can be obtained, respectively, in 92.8% and 85.7% selectivities, 71.7% and 80.4% current efficiencies, with 1.21 and 1.08 kg.h-1.m-2 productivities and power consumptions of 2.94 and 4.1 kWh.kg-1 using undivided cells and aqueous K2HPO4 electrolysis media at pHs of 3.6 and 5.5. The reported electroconversion of acetoin is highly flexible because 2,3-BD and MEK can be produced by changing just the cathode but using the same cell, with the same electrolyte at the same current density.