Related Experiment Video
Updated: Jun 27, 2026

Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Ultra-Low Pt Loading Bimetallic PtNi Catalyst on Nano-LTL Zeolite for the Selective Hydrogenation of
Zhen Liu1,2, Guoan Xi1,2, Yin Hu1
1Key Laboratory of Jiangxi Province for Environment and Energy Catalysis, Institute of Materials and Intelligent Manufacturing, Jiangxi Academy of Sciences, Nanchang 330096, China.
Abstract:
The selective hydrogenation of p-chloronitrobenzene (p-CNB) to p-chloroaniline (p-CAN) is of great importance for the production of dyes, pesticides, and pharmaceuticals, but it is often plagued by the undesired hydrodechlorination side reaction. In this work, we report a PtNi bimetallic catalyst supported on nano-sized LTL zeolite (PtNi/Nano-HL) for the selective hydrogenation of p-chloronitrobenzene under mild conditions. The catalyst was systematically characterized by X-ray diffraction (XRD), nitrogen sorption (N2 sorption), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and ammonia temperature-programmed desorption (NH3-TPD). The results reveal abundant oxygen vacancies (RIR = 0.73) and an optimized distribution of medium-strong acid sites on the catalyst surface, as well as electronic interaction between Pt and Ni, which collectively enhance the catalytic performance. Remarkably, the PtNi/Nano-HL catalyst achieves 100% conversion and over 99% selectivity for p-chloroaniline under ambient conditions (30 °C, 0.1 MPa H2) using ethanol as a solvent. Even after 24 recycling runs, it retains 100% conversion and >93% selectivity, demonstrating excellent stability. Moreover, the catalyst requires an extremely low Pt loading (only 0.11 wt%) and exhibits good substrate universality for various substituted nitroarenes. This work provides a promising strategy for designing high-performance bimetallic catalysts on nano-zeolite supports for the selective hydrogenation of halonitrobenzenes.
Related Concept Videos
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,...
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...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
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 surface of...
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.
Reactions at the Benzylic Position: Halogenation

