Abstract
The etherification of glycerol with tert-butyl alcohol in the presence of acid catalysts gives rise to the production of ethers (monoethers, diethers and triethers) of high added-value, which can be used as oxygenated additives in fuels. This reaction is limited by the thermodynamic equilibrium, which can be modified by the addition of solvents that selectively solubilize the products of interest along with tert-butyl alcohol, leading to the progress of the reaction. In this work, it has been demonstrated that the addition of dibutyl ether allows shifting the reaction equilibrium, increasing the production of diethers. From the study of the main operating conditions, it was determined that an increase in the concentration of the solvent has a positive effect on the selectivity towards the production of diethers, the concentration of the catalyst (a commercial ion exchange resin, Amberlyst 15, named A-15) and the reaction temperature were also determining variables. Working with concentrations of tert-butyl alcohol above the stoichiometric one did not report great advantages. The optimal operating conditions to maximize the conversion of glycerol and the selectivity towards diethers were: 70 °C, 20% catalyst (referred to the total starting mass of the system), the stoichiometric ratio of glycerol:tert-butyl alcohol (G:TB = 1:3) and 1:2 molar ratio of dibutyl ether:tert-butyl alcohol. A study of three consecutive reaction cycles showed the high stability of the catalyst, obtaining identical results.
Highlights
The renewable and biodegradable character of biodiesel has made it an interesting alternative to the use of conventional fuels [1,2,3]
The aim of introducing dibutyl ether (DBE) as a solvent in the etherification reaction between tert-butyl alcohol (TB) and G is to improve the production of diethers
(to continue the etherification reaction), are selectively solubilized in the organic phase (DBE), keeping most of the water generated in the other phase
Summary
The renewable and biodegradable character of biodiesel has made it an interesting alternative to the use of conventional fuels [1,2,3]. There are several industrial processes that use glycerol as raw material (oligomerization/polymerization, pyrolysis and gasification, selective oxidation, steam reforming, selective transesterification, etherification to fuel-oxygenates, etc.) [12,13]. Another alternative is the production of glycerol carbonate (an important glycerol derivative commonly used as a solvent in cosmetics, personal care items and medicine) from the catalytic oxidative carbonylation of the parent compound [14]. An interesting alternative for the excess of glycerol generated is its transformation into oxygenated additives
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