Related Experiment Video
Updated: Dec 4, 2025

A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
Published on: March 29, 2019
Regeneration of [Bmim]BF4 ionic liquid by ozonation: hydrogen bond roles, synergistic effect, and DFT calculation
Jingyu Ren1,2,3, Jie Li4, Lei Lv5,6
1School of Petroleum Engineering and Environmental Engineering, Yan'an University, Yan'an, 716000, China. renjingyuyau@163.com.
Abstract:
Ionic liquids (ILs) are a kind of promising extractants for removing undesirable organics from industrial wastewater and crude oil, etc. Herein, IL regeneration by ozonation was proposed for its recycling. 1-Butyl-3-methylimidazolium tetrafluoroborate ([Bmim]BF4) and phenol were used as the representative IL and organic matter, respectively. The regeneration performance, stability of [Bmim]BF4, and roles of hydrogen bonds between O3 and [Bmim]BF4 in the phenol removal were studied. The experimental results showed that 90.2% of phenol was degraded in [Bmim]BF4 after ozonation treatment for 30 min with the O3 concentration of 1.2 mg/L. The nonvolatility of [Bmim]BF4-made phenol was adequately degraded, while the concentration of phenol increased during ozone treatment in the conventional extractants (ethanol, ethyl acetate, and dichloromethane) due to their high volatility. The reuse experiments, spectra of Fourier transform infrared spectroscopy and 1H nuclear magnetic resonance spectroscopy indicated that [Bmim]BF4 was steady under the ozonation process. Density functional theory simulation confirmed that hydrogen bonds between [Bmim]+ and O3 could be formed, and calculational results of Hirshfeld charges indicated that the nucleophilicity of O3 was enhanced by the hydrogen bonds. The enhanced nucleophilicity resulted in the increase of phenol degradation efficiency by ozonation, and the synergistic effect between O3 and ILs was proportional to the hydrogen bond donor ability of ILs.
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
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...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Radical Formation: Homolysis

