Abstract
Hydrogen production from aluminum-water reactions is often limited by the formation of a passive alumina (Al2O3) layer that hinders reactivity. In this study, a new system was developed by incorporating sodium aluminate (NaAlO2) into a sodium hydroxide (NaOH) solution, with all parameters, room temperature and pH 13, kept constant to isolate the effect of solution composition. A maximum hydrogen yield of 77.4 % was achieved at a NaAlO2 concentration of 0.5 M. In-situ electrochemical characterization showed that the reaction is governed by charge transfer across three stages: Al2O3 hydration, formation of Al(OH)4− accompanied by hydrogen release, and subsequent conversion to Al(OH)3. The precipitation of Al(OH)3 occurs in two phases gibbsite and bayerite through fast and slow reaction pathways, respectively. These pathways governed by solution stability, as a NaOH + NaAlO2 mixture tends to destabilize Al(OH)3 precipitation.
| Original language | English |
|---|---|
| Pages (from-to) | 112-120 |
| Number of pages | 9 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 143 |
| DOIs | |
| Publication status | Published - 1 Jul 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Al(OH)
- Aluminum
- Electrochemical
- Hydrogen
- Water
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