Hydrogen sorption mechanisms in lithium amide and metal hydride reactive systems.
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Considerable effort has been devoted to the M-N-H system for solid-state hydrogen
storage. However, the desorption mechanism is still unclear and the desorption
temperature is too high for practical considerations. Here, the desorption characteristics
of LiNH2 and a mixture of (LiNH2+LiH) were firstly comparatively studied by
simultaneous then-nogravimetry, differential scanning calorimetry and mass
spectrometry for further understanding of H2 desorption in the (LiNH2+LiH) system.
Mass spectrometry and thermal analysis of (LiNH2+LiH) mixtures indicate that
approximately 5 mass % of H2 is released at 180*C after four hours of milling without
any apparent release of NH3, whereas insufficient mixing of the two compounds cannot
stop the escaping of NH3 from the mixture. Non-unifon-ri mixing can lead to the escape
of NH3 from the mixture. The evidence further supports the notion that NH3
intermediated reaction is a possible reaction path within the thermal desorption of the
(LiNH2+ LiH) mixture. BN additive, among selected nitrides shows the best effect on
desorption from (LiNH2+ LiH). (LiNH2+MgH2)materials with different molar ratios
(4: 3,4: 2 and 4: 1) were also studied for their sorption properties and mechanisms.
Results show that more than 6 mass% H2 is desorbed from 1500C for the (4LiNH2
+3MgH2)mixture, with two H2peaks at 200 and 320'C. Meanwhile, there is only -5
mass% for (4LiNH2 +2MgH2) mixture with one H2 peak at 200 T. Reversibility
measurements suggest that LiNH2 and MgH2 cannot be recovered after absorption;
instead, Li2NH and Mg(NH2)2 (or MgNH) take over to perform the H2 storage functions.
The (4LiNH2+3MgH2 ) mixture possess a greater H2 capacity in first desorption, but
shows less than 2 mass% reversible capacity in subsequent cycles. However, there is
only about I mass% capacity loss during the reversibility measurement for the (4LiNH2
+2MgH2)mixture. Other M-N-H systems, mainly NaH, KH, AlH3 and CaH2, were also
investigated, and only CaH2 shows the capability of reacting with LiNH2 to produce H2
among these candidates.
Authors
Yao, JinhanCollections
- Theses [3706]