Related Experiment Video
Updated: Sep 24, 2025

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Highly effective carbon-supported gold-ionic liquid catalyst for acetylene hydrochlorination
Xueyan Qi1,2, Weifeng Chen3, Jinli Zhang2
1College of Materials Science and Engineering, Hebei University of Engineering Handan 056038 Hebei PR China qixueyan001@163.com.
A novel non-mercuric catalyst using trimethylsulfonium iodide (C3H9SI) and gold on active carbon (Au-IL/SAC) shows high efficiency and stability for acetylene hydrochlorination, offering a greener alternative.
Area of Science:
- Catalysis
- Materials Science
- Green Chemistry
Background:
- Acetylene hydrochlorination traditionally uses mercury-based catalysts, posing environmental risks.
- Developing efficient, non-mercuric catalysts is crucial for sustainable industrial processes.
Purpose of the Study:
- To synthesize and evaluate a novel non-mercuric catalyst for acetylene hydrochlorination.
- To investigate the role of a sulfur-containing ionic liquid (trimethylsulfonium iodide, C3H9SI) in catalyst performance.
Main Methods:
- Synthesis of gold-ionic liquid/spherical active carbon (Au-IL/SAC) catalysts via incipient wetness impregnation.
- Testing catalytic performance in acetylene hydrochlorination under various conditions.
- Characterization using BET, TGA, TPD, XRD, TEM, and XPS.
Main Results:
- The 0.3% Au-IL/SAC catalyst achieved 90% acetylene conversion at 170 °C and 360 h⁻¹ GHSV.
- The catalyst demonstrated excellent stability, maintaining 97% conversion for 200 hours.
- C3H9SI improved gold dispersion and inhibited coke deposition.
Conclusions:
- The Au-IL/SAC catalyst is a highly active and stable non-mercuric alternative for acetylene hydrochlorination.
- The ionic liquid additive plays a key role in enhancing catalyst performance and longevity.
- This catalyst presents a promising green option for industrial applications.
More Related Videos
11:02Synthesis and Catalytic Performance of Gold Intercalated in the Walls of Mesoporous Silica
Published on: July 9, 2015
08:40Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Related Concept Videos
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
Catalysis