Related Experiment Video
Updated: Sep 30, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Ti3AlC2/Pd Composites for Efficient Hydrogen Production from Alkaline Formaldehyde Solutions
Xiaogang Liu1, Wenjie Chen1, Xin Zhang1
1College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang 464000, China.
Abstract:
Research on catalytic oxidation in a promising but mild manner to remove formaldehyde and produce hydrogen is rarely reported. Here, the use of the Ti3AlC2 MAX phase as support for palladium nanoparticles was explored for the hydrogen generation from alkaline formaldehyde solution at room temperature. The results showed that Ti3AlC2/Pd catalyst with 3 wt% Pd loading had a much higher capability for hydrogen production than conventional Pd nanoparticles. In addition, by further optimizing the formaldehyde concentration, NaOH concentration, and the reaction temperature, the hydrogen production rate could be further increased to 291.6 mL min-1g-1. Moreover, the obtained apparent activation energy of the Ti3AlC2/Pd catalyzed hydrogen production reaction is 39.48 kJ mol-1, which is much lower than that of the literature results (65 kJ mol-1). The prepared Ti3AlC2/Pd catalysts as well as the catalytic process could act as a "two birds with one stone" effect, that is, they not only eliminate noxious formaldehyde but also generate clean hydrogen.
Related Concept Videos
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...
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...
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...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Carboxylic Acids to Primary Alcohols: Hydride Reduction

