The gas-phase hydroxyl (OH) radical emission was observed in the thermal decomposition of lithium hydroxide (LiOH). This phenomenon was investigated in a vacuum flow tube reactor at around 2 Torr by the temperature programmed reaction (TPR) experiments at 500-1300 K. The production of OH and other gaseous products was quantitatively investigated by the laser induced fluorescence method and quadrupole mass spectrometry, respectively. The TPR spectra of OH had a peak at 1100-1200 K, which largely exceeded the gas-phase thermodynamic equilibrium. The origin of OH was supposed to be either the surface OH groups on Li2O or the residual LiOH in the LiOH/Li2O solid solution. OH production exceeding the thermodynamic equilibrium was explained by means of the partial equilibrium in the reaction: LiOH + 1/4O2 ⇔ 1/2Li2O + OH. This phenomenon can be a new route for the OH production from H2O and O2 in cyclic reactions of lithium compounds.
|Number of pages||6|
|Journal||Journal of Physical Chemistry B|
|Publication status||Published - 1999 Mar 18|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Surfaces, Coatings and Films
- Materials Chemistry