Issue 3, 2012

Promoted hydrogen release from ammonia borane with mannitolvia a solid-state reaction route

Abstract

Promoted hydrogen release from ammonia borane (NH3BH3, AB) with mannitol (C6H8(OH)6, MA) additive is reported. It is found that for the MA/2AB sample, the dehydrogenation temperature is lowered by ∼25 °C compared to that of neat AB, the liberation of undesired byproduct borazine is suppressed, and the released ammonia can be removed by using anhydrous MgCl2 as absorber. The analyses of Raman, Fourier transform infrared spectroscopy and 11B nuclear magnetic resonance spectroscopy demonstrate the breaking of B–N, B–H and O–H bonds and the formation of B–O bonds for the dehydrogenation process of MA/2AB. These results suggest a solid-state dehydrogenation reaction between AB and MA: the B–Hδ bonds in AB and the O–Hδ+ bonds in MA combine with each other to release H2. Furthermore, the use of the perfect –OH carrier MA as additive leads to a straightforward understanding of the improved dehydrogenation of AB under the effect of hydroxyl groups in the solid state.

Graphical abstract: Promoted hydrogen release from ammonia borane with mannitolvia a solid-state reaction route

Article information

Article type
Paper
Submitted
20 Aug 2011
Accepted
02 Oct 2011
First published
14 Nov 2011

Dalton Trans., 2012,41, 871-875

Promoted hydrogen release from ammonia borane with mannitolvia a solid-state reaction route

Y. Pan, Y. Wang, Y. Liang, Z. Tao and J. Chen, Dalton Trans., 2012, 41, 871 DOI: 10.1039/C1DT11567G

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