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Effect of several metal chlorides on the thermal decomposition behaviour of α-Mg(BH 4) 2
Mechanochemical alloying of Mg(BH 4) 2 with small amounts of metal chlorides (PdCl 2, TiCl 3, VCl 3, MoCl 3, RuCl 3, CeCl 3 and NbCl 5) results in the formation of transition metal doped nanocomposites with different hydrogen desorption properties. The thermal decomposition properties of ball-milled...
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Published in: | International journal of hydrogen energy 2011-09, Vol.36 (19), p.12313-12318 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Mechanochemical alloying of Mg(BH
4)
2 with small amounts of metal chlorides (PdCl
2, TiCl
3, VCl
3, MoCl
3, RuCl
3, CeCl
3 and NbCl
5) results in the formation of transition metal doped nanocomposites with different hydrogen desorption properties. The thermal decomposition properties of ball-milled as well as doped α-Mg(BH
4)
2 have been studied. An amorphization reaction of Mg(BH
4)
2 is induced by ball milling, nevertheless a partial recrystallization of the alpha phase takes place after heating up to 150 °C. The effect of ball milling Mg(BH
4)
2 with each additive has been investigated in detail by using differential scanning calorimetry, thermogravimetric analysis and X-ray diffraction. The onset temperature of Mg(BH
4)
2 is lowered by more than 100 °C through the addition of Nb- or Ti chloride. Moreover, a mixed Ti-Nb-nanocomposite was also synthesized and investigated. The onset temperature of hydrogen evolution during decomposition of the mixed Ti-Nb-nanocomposite is considerably lowered by up to 125 °C.
► Transition metal chlorides as dopants of magnesium borohydride. ► Thermal decomposition behaviour of several nanocomposites investigated. ► Onset temperature of Ti–Ni nanocomposite lowered up to 125 °C. ► Improvement of the hydrogen desorption properties of magnesium borohydride. |
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ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2011.07.008 |