Skip to content

Chemistry · Ch 9 — Hydrogen

Preparation

9.7.1

Preparation

Preparing Hydrogen Peroxide

1. From barium peroxide. Acidifying barium peroxide octahydrate with sulphuric acid, then removing excess water by evaporation under reduced pressure, gives hydrogen peroxide:

BaO2⋅8H2O(s)+H2SO4(aq)→BaSO4(s)+H2O2(aq)+8H2O(l)BaO_2\cdot8H_2O(s) + H_2SO_4(aq) \rightarrow BaSO_4(s) + H_2O_2(aq) + 8H_2O(l)

2. Via peroxodisulphate. Electrolytic oxidation of acidified sulphate solutions at high current density gives peroxodisulphuric acid, which is then hydrolysed to release hydrogen peroxide:

2HSO4−(aq)→electrolysisHO3SOOSO3H(aq)→hydrolysis2HSO4−(aq)+2H+(aq)+H2O2(aq)2HSO_4^-(aq) \xrightarrow{\text{electrolysis}} HO_3SOOSO_3H(aq) \xrightarrow{\text{hydrolysis}} 2HSO_4^-(aq) + 2H^+(aq) + H_2O_2(aq)

This same route, run with D2OD_2O, is now the standard laboratory preparation of deuterium peroxide, D2O2D_2O_2:

K2S2O8(s)+2D2O(l)→2KDSO4(aq)+D2O2(l)K_2S_2O_8(s) + 2D_2O(l) \rightarrow 2KDSO_4(aq) + D_2O_2(l)

3. Industrial route — auto-oxidation of 2-alkylanthraquinols. This is the process used at scale:

2-ethylanthraquinol→O2(air)/H2, PdH2O2+(oxidised product)\text{2-ethylanthraquinol} \xrightarrow{O_2(\text{air})/H_2,\ Pd} H_2O_2 + \text{(oxidised product)} …