Related Experiment Video
Updated: Sep 27, 2025

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Design of choline chloride modified USY zeolites for palladium-catalyzed acetylene hydrochlorination
Zeqing Long1, Lu Wang1, Haijun Yan1
1Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education, Xinjiang Uyghur Autonomous Region, School of Chemical Engineering and Technology, Xinjiang University Urumqi 830017 China wanglu_4951@163.com +86-0991-8581018 +86-0991-8581018.
Abstract:
USY zeolites (USY) were applied to design and synthesize palladium-based heterogeneous catalysts for exploring an efficient non-mercuric catalyst for acetylene hydrochlorination. Choline chloride (ChCl) was selected as the nitrogen-containing ligand to modify the Pd@USY catalysts and the proposed Pd@15ChCl@USY catalyst exhibited obviously the best catalytic performance with a stable acetylene conversion and vinyl chloride selectivity of over 99.0% for more than 20 h. According to the results of characterization and the density functional theory calculations, it is indicated that the addition of ChCl can significantly inhibit the agglomeration and loss of the Pd active species, prevent carbon deposition and enhance the ability of HCl and C2H2 adsorption and C2H3Cl desorption, resulting in promoting the catalytic performance of Pd@USY catalysts during the acetylene hydrochlorination reaction.
More Related Videos
19:58Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
Published on: July 30, 2017
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Related Concept Videos
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...
Preparation of Alkynes: Alkylation Reaction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
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.
Preparation of Alkynes: Dehydrohalogenation
Alkynes can be prepared by dehydrohalogenation of vicinal or geminal dihalides in the presence of a strong base like sodium amide in liquid ammonia. The reaction proceeds with the loss of two equivalents of hydrogen halide (HX) via two successive E2 elimination reactions.
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