Related Experiment Video
Updated: Jul 4, 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
Producing Alkali Metal Hydrides from Hydroxides.
Ainee Ibrahim1, Mark Paskevicius1, Terry D Humphries1
1Physics and Astronomy, Institute for Energy Transition, Curtin University, GPO Box U1987, Perth, WA 6845, Australia.
Researchers developed a cost-effective method to produce alkali metal hydrides from hydroxides. This novel process simplifies purification and shows potential for sodium borohydride applications.
Area of Science:
- Inorganic Chemistry
- Materials Science
- Chemical Engineering
Background:
- Alkali metal hydrides are crucial chemical intermediates.
- Existing production methods can be complex and costly.
- There is a need for efficient and scalable hydride synthesis.
Purpose of the Study:
- To present a novel, cost-effective method for producing alkali metal hydrides (NaH, KH, RbH, CsH) from their corresponding metal hydroxides.
- To investigate various metallic reducing agents for sodium hydride (NaH) production from sodium hydroxide (NaOH).
- To explore the potential of this NaH production method for sodium borohydride (NaBH4) applications and hydrogen export.
Main Methods:
- Reactions conducted in an autoclave reactor under controlled conditions (250 °C, 14 bar H2 pressure) using paraffin oil.
- Investigated metallic reducing agents including Mg, Al, Si, CaH2, Cr, Mn, and Sr for NaH synthesis.
- Implemented a two-step process involving metal formation followed by hydrogenation to simplify purification.
Main Results:
- Successfully produced various alkali metal hydrides from their respective hydroxides.
- Identified effective metallic reducing agents for NaH production.
- Demonstrated that a two-step process enhances separation and purification of metal hydrides.
Conclusions:
- The presented method offers a viable, cost-effective alternative for alkali metal hydride production.
- The process is adaptable for producing sodium hydride, with implications for sodium borohydride synthesis and hydrogen storage.
- This research contributes to advancing efficient chemical synthesis and hydrogen economy technologies.
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...
Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids
Reducing carboxylic acid derivatives like acyl chlorides (RCOCl), esters (RCO2R′), and nitriles (RCN) using milder aluminum hydride agents like lithium tri-tert-butoxyaluminum hydride [LiAlH(O-t-Bu)3] and diisobutylaluminum hydride [DIBAL-H]...
Hydroboration-Oxidation of Alkenes
Carboxylic Acids to Primary Alcohols: Hydride Reduction
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...
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...

