Activated aluminum pellets meet water; the passivating oxide is stripped by a liquid‑metal alloy and the bare metal splits water into hydrogen. Fuel that is a solid you can hold, water you can find, and an exhaust that is water again.
Exothermic hydrolysis, aqueous, near‑ambient pressure, optimal ~50 °C. Bare aluminum reduces water; the metal is oxidized to hydroxide and hydrogen is liberated. Under reactor heat some Al(OH)3 dehydrates to boehmite: Al(OH)₃ → AlOOH + H₂O.
The oxide skin (Al2O3) that normally passivates aluminum in air is disrupted by a gallium‑indium liquid‑metal alloy penetrating the grain boundaries, keeping fresh metal exposed. Imidazole acts as a bifunctional proton‑transfer catalyst, accelerating hydrolysis roughly 24× versus plain water.
| Quantity (per kg Al) | Value |
|---|---|
| moles Al | 37.06 mol |
| H₂ yield (stoich.) | 0.1121 kg |
| H₂O consumed | ~2.00 kg |
| Boehmite (AlOOH) | 2.224 kg |
| Reaction heat ΔH | 15.49 MJ |
| H₂ energy (LHV) | 12.92 MJ |
CHEMISTRY.md / SPECS.md in this repo.
With activation OFF the catalyst multiplier collapses toward ~1/24 of nominal (the uncatalysed plain‑water rate) and the oxide is only slowly breached — the numbers fall accordingly. Range uses the SPECS reference chain: 3.876 kg H₂ per 36 kg cartridge → 80.1 kWh → ≈400 km at a 15 kW / 80 km·h⁻¹ average draw.
2Al + 6H₂O → 2Al(OH)₃ + 3H₂, its ~0.112 kg H₂/kg Al stoichiometry, the ΔH ≈ −418 kJ/mol exothermicity, and the H₂ energy content (LHV 120 MJ/kg) are established chemistry, correctly implemented here from first principles.