Thermochemical transformations in 2MNH(2)-3MgH(2) systems (M = Li or Na)
| Title | Thermochemical transformations in 2MNH(2)-3MgH(2) systems (M = Li or Na) |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | Dolotko O, Paulson N, Pecharsky VK |
| Journal Title | International Journal of Hydrogen Energy |
| Volume | 35 |
| Pages | 4562-4568 |
| Date Published | 05/01 |
| ISBN Number | 0360-3199 |
| Accession Number | ISI:000278418700013 |
| Keywords | amides, complex hydrides, destabilization, h system, hydrides, hydrogen release, hydrogen storage-system, imides, mg3n2, temperature programmed dehydrogenation, x-ray diffraction |
| Abstract | Thermochemical reactions between alkali metal amides and magnesium hydride taken in 2:3 molar ratios have been investigated using pressure-composition-temperature, X-ray powder diffraction and residual gas analysis measurements. The thermally induced reactions in both title systems are stoichiometric and proceed as a following solid state transformation: 2MNH(2)+ 3MgH(2) -> Mg3N2 + 2MH + 4H(2)up arrow. A total of 6.45 wt.% of hydrogen is released by the 2LiNH(2)-3MgH(2) system beginning at 186 degrees C, and a total of 5.1 wt.% H-2 is released by the 2NaNH(2)-3MgH(2) system starting at 130 degrees C. Combined structure/property investigations revealed that the transformation in the lithium containing system proceeds in two steps. In the first step, lithium amide reacts with MgH2 to form Li2Mg(NH)(2) and hydrogen. In the second step, reaction between Li2Mg(NH) and MgH2 leads to the formation of the Mg3N2 nitride, lithium hydride and additional gaseous hydrogen. The transformation in the sodium containing system appears to proceed through a series of competing solid state processes with formation of Mg(NH2)(2) and NaMgH3 intermediates. Partial rehydrogenation in 190 bar hydrogen pressure leading to formation of the MgNH imide was observed in the dehydrogenated 2NaNH(2)-3MgH(2) system at 395 degrees C. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved. |
| URL | <Go to ISI>://000278418700013 |
| DOI | Doi 10.1016/J.Ijhydene.2010.02.104 |
















