Related Experiment Video
Updated: Feb 13, 2026

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
Published on: February 7, 2017
Palladium Supported on Titanium Carbide: A Highly Efficient, Durable, and Recyclable Bifunctional Catalyst for the
Guangyin Fan1, Xiaojing Li2, Caili Xu3
1College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610068, China. fanguangyin@sicnu.edu.cn.
Abstract:
Developing highly efficient and recyclable catalysts for the transformation of toxic organic contaminates still remains a challenge. Herein, Titanium Carbide (Ti₃C₂) MXene modified by alkali treatment process was selected as a support (designated as alk-Ti₃C₂X₂, where X represents the surface terminations) for the synthesis of Pd/alk-Ti₃C₂X₂. Results show that the alkali treatment leads to the increase of surface area and surface oxygen-containing groups of Ti₃C₂X₂, thereby facilitating the dispersion and stabilization of Pd species on the surface of alk-Ti₃C₂X₂. The Pd/alk-Ti₃C₂X₂ catalyst shows excellent catalytic activity for the hydrodechlorination of 4-chlorophenol and the hydrogenation of 4-nitrophenol in aqueous solution at 25 °C and hydrogen balloon pressure. High initial reaction rates of 216.6 and 126.3 min-1· g pd - 1 are observed for the hydrodechlorination of 4-chlorophenol and hydrogenation of 4-nitrophenol, respectively. Most importantly, Pd/alk-Ti₃C₂X₂ exhibits excellent stability and recyclability in both reactions without any promoters. The superior property of Pd/alk-Ti₃C₂X₂ makes it as a potential material for practical applications.
Related Concept Videos
Dipeptidyl Peptidase 4 Inhibitors
Piaget's Stage 4 of Cognitive Development
Abstract Reasoning and Hypothetical-Deductive Thinking
Unlike the concrete operational...
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Criteria for Aromaticity and the Hückel 4n + 2 Rule
For the first time, Eric Hückel, a German chemical physicist, derived a set of structural features for a compound to be classified as aromatic. This is now known as Hückel’s rule or the 4n +...

