Crude glycerol esterification using biomass-derived carbon acid catalysts

In this work, carbons obtained from peanut shells (PC), activated with KOH (APC) and functionalized with H2SO4 (PC-F and APC-F, respectively) were evaluated as catalysts in the esterification of crude glycerol with acetic acid to obtain monoacetyl glycerol, diacetyl and triacetyl glycerol. The chara...

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Bibliographic Details
Main Authors: Federico M. Perez, Martín N. Gatti, Carla S. Fermanelli, Clara Saux, M. Soledad Renzini, Francisco Pompeo
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Next Materials
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2949822824000224
Description
Summary:In this work, carbons obtained from peanut shells (PC), activated with KOH (APC) and functionalized with H2SO4 (PC-F and APC-F, respectively) were evaluated as catalysts in the esterification of crude glycerol with acetic acid to obtain monoacetyl glycerol, diacetyl and triacetyl glycerol. The characterization revealed that both PC-F and APC-F have high specific surface areas and very strong acid sites due to the presence of -HSO3 groups. The activity of both catalysts was evaluated using crude glycerol obtained from biodiesel synthesis, which presented acid pH, water, methanol, Na2SO4 and non-glycerol organic matter (MONG) as major impurities. The APC-F catalyst was more active than PC-F due to the combination of its surface acidity and textural properties. After 5 reaction cycles at 120 °C, using an acetic acid/glycerol molar ratio of 6 and a catalyst/glycerol mass ratio of 0.25, APC-F showed a decrease in specific surface area and pore volume due to the adsorption of Na2SO4 present in the crude glycerol. However, it was able to maintain activity levels with 100% glycerol conversion and selectivity to monoacetyl glycerol, diacetyl glycerol and triacetyl glycerol of 55%, 35% and 10%, respectively.
ISSN:2949-8228