Related Experiment Video
Updated: May 18, 2026

Techniques for the Evolution of Robust Pentose-fermenting Yeast for Bioconversion of Lignocellulose to Ethanol
Published on: October 24, 2016
Valorization of glycerol via continuous etherification with ethanol: Thermodynamic modeling and process optimization
Carolina M Marinho1, Caroline O T Lemos1, Karen A Resende1
1Faculdade de Engenharia Química, Universidade Federal de Uberlândia, Av. João Naves de Ávila 2121, Campus Santa Mônica - Bloco 1K, 38400-902 Uberlândia, MG, Brazil.
Abstract:
The valorization of glycerol into value-added chemicals is essential for improving the sustainability of biodiesel and biorefinery systems. This study integrates a thermodynamic vapor-liquid equilibrium model with experimental etherification data to optimize superheated vapor-phase conversion of glycerol using ethanol. Phase behavior of the ethanol-glycerol system was predicted using the Peng-Robinson equation of state with classical van der Waals mixing rules. Experimental investigations evaluated the effects of temperature (210-370°C), catalyst loading (0-0.95 g), ethanol-to-glycerol molar ratio (4:1-30:1), and pressure (7-103 MPa) over a β-zeolite catalyst. Under optimized conditions, a maximum ether yield of 50% and glycerol conversion of 83% were achieved, showing competitive performance compared with existing glycerol upgrading technologies, particularly under continuous fixed-bed operation. Maintaining the reaction system in a single-phase superheated vapor state at moderate pressure (7.9 MPa) and elevated temperature (319°C) effectively reduced mass-transfer limitations typical of biphasic systems. The results demonstrate the potential of superheated vapor-phase processing as an efficient route for glycerol waste valorization and provide guidance for process optimization and scale-up toward sustainable chemical production.
Related Concept Videos
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more substituted...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Physical Properties of Ethers
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...

