4.7 Article

Effect of initial pH on hydrothermal decomposition of cellobiose under weakly acidic conditions

Journal

FUEL
Volume 158, Issue -, Pages 315-321

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2015.05.023

Keywords

Biofuel; Cellobiose; Hydrothermal; Isomerization; Acidic conditions

Funding

  1. Centre for Research into Energy for Sustainable Transport (CREST) through the Western Australian Government Centre of Excellence Program
  2. Australian Research Council's Discovery Projects Program
  3. Malaysian Agricultural Research and Development Institute (MARDI)

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The paper reports the cellobiose hydrothermal decomposition at 200-250 degrees C under non-catalytic (with an initial pH close to 7) and weakly acidic conditions (with an initial pH of 4-6). It was found cellobiose decomposition under both non-catalytic and weakly acidic conditions follows similar primary decomposition pathways, i.e., isomerization and hydrolysis reactions being the main primary reactions. However, cellobiose decomposition under acidic conditions decreases the selectivities of isomerization reactions but increases the selectivity of hydrolysis reaction. While the rate constants of isomerization reactions under various pH conditions are found to be similar, that of hydrolysis reaction increases significantly with reducing the initial pH of the solution. Therefore, the acceleration of cellobiose decomposition under acidic conditions is mainly due to the increased contribution of hydrolysis reaction. Further analysis suggests that the rate constant of hydrolysis reaction is dependent on the hydrogen ion concentration of the solution at reaction temperature. A kinetic model was then developed, considering the isomerization and hydrolysis reactions. The model can well predict the cellobiose hydrothermal decomposition under various initial pH conditions at low temperatures (i.e., <225 degrees C). However, the model underestimates the rate constant of cellobiose hydrothermal decomposition at higher temperatures (i.e., 250 degrees C), suggesting the increased contribution of other reactions (e.g., reversion reactions) under the conditions. (C) 2015 Elsevier Ltd. All rights reserved.

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