Related Experiment Video
Updated: Sep 23, 2025

Organic Structure-directing Agent-free Synthesis for *BEA-type Zeolite Membrane
Published on: February 22, 2020
Insight into the active site nature of zeolite H-BEA for liquid phase etherification of isobutylene with ethanol
Nina V Vlasenko1, Yuri N Kochkin1, German M Telbiz1
1L. V. Pisarzhevskii Institute of Physical Chemistry, National Academy of Sciences of Ukraine Prospect Nauki 31 03039 Kiev Ukraine nvvlasenko@gmail.com.
Abstract:
The nature of active acid sites of zeolite H-BEA with different Si/Al ratios (15-407) in liquid phase etherification of isobutylene with ethanol in a continuous flow reactor in the temperature range 80-180 °C has been explored. We describe and discuss data concerning the strength and concentration of acid sites of H-BEA obtained by techniques of stepwise (quasi-equilibrium) thermal desorption of ammonia, X-ray diffraction, low-temperature adsorption of nitrogen, FTIR spectroscopy of adsorbed pyridine and solid-state 27Al MAS NMR. The average values of the adsorption energy of NH3 on H-BEA were experimentally determined as 63.7; 91.3 and 121.9 mmol g-1 (weak, medium, and strong, respectively). In agreement with this, a correlation between the rate of ethyl-tert-butyl ether synthesis and the concentration of weak acid sites (E NH = 61.6-68.9 kJ mol-1) has been observed. It was concluded that the active sites of H-BEA for this reaction are Brønsted hydroxyls representing internal silanol groups associated with octahedrally coordinated aluminum in the second coordination sphere.
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...
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene
Hydroboration-Oxidation of Alkenes
Acid-Catalyzed Dehydration of Alcohols to Alkenes
E2 Reaction: Stereochemistry and Regiochemistry
When a substrate with two different β hydrogens undergoes an E2 elimination, the presence of a strong base can yield two regioisomeric alkenes. The more-substituted alkene is the major...

