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Study of Morphological Changes in MgH2 Destabilized LiBH4 Systems Using Computed X-ray Microtomography

Journal Article · · Materials
DOI:https://doi.org/10.3390/ma5101740· OSTI ID:1628435
 [1];  [2];  [3]
  1. Rowan Univ., Glassboro, NJ (United States). Dept. of Physics and Astronomy; DOE/OSTI
  2. Louisiana Tech Univ., Ruston, LA (United States). Inst. for Micromanufacturing. Dept. of Chemical Engineering
  3. Louisiana State Univ., Baton Rouge, LA (United States). Dept. of Chemistry
The objective of this study was to apply three-dimensional x-ray microtomographic imaging to understanding morphologies in the diphasic destabilized hydride system: MgH2 and LiBH4. Each of the single phase hydrides as well as two-phase mixtures at LiBH4:MgH2 ratios of 1:3, 1:1, and 2:1 were prepared by high energy ball milling for 5 minutes (with and without 4 mol % TiCl3 catalyst additions). Samples were imaged using computed microtomography in order to (i) establish measurement conditions leading to maximum absorption contrast between the two phases and (ii) determine interfacial volume. The optimal energy for measurement was determined to be 15 keV (having 18% transmission for the MgH2 phase and above 90% transmission for the LiBH4 phase). This work also focused on the determination of interfacial volume. Results showed that interfacial volume for each of the single phase systems, LiBH4 and MgH2, did not change much with catalysis using 4 mol % TiCl3. However, for the mixed composite system, interphase boundary volume was always higher in the catalyzed system; increasing from 15% to 33% in the 1:3 system, from 11% to 20% in the 1:1 system, and 2% to 14% in the 2:1 system. The parameters studied are expected to govern mass transport (i.e., diffusion) and ultimately lead to microstructure-based improvements on H2 desorption and uptake rates.
Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences & Engineering Division
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1628435
Journal Information:
Materials, Journal Name: Materials Journal Issue: 10 Vol. 5; ISSN 1996-1944; ISSN MATEG9
Publisher:
MDPICopyright Statement
Country of Publication:
United States
Language:
English

References (11)

Bulk observation of metal powder sintering by X-ray synchrotron microtomography journal February 2004
Ultrasmall-angle X-ray scattering (USAXS) studies of morphological trends in high energy milled NaAlH4 powders journal October 2007
Hydrogen storage in destabilized chemical systems journal May 2007
Investigation of the Sintering of Heterogeneous Powder Systems by Synchrotron Microtomography and Discrete Element Simulation journal July 2009
X-ray tomography system, automation, and remote access at beamline 2-BM of the Advanced Photon Source conference August 2006
In situ microtomography investigation of metal powder compacts during sintering journal January 2003
Reaction of hydrogen with alloys of magnesium and copper journal December 1967
Reversible Storage of Hydrogen in Destabilized LiBH 4 journal March 2005
Identification of Destabilized Metal Hydrides for Hydrogen Storage Using First Principles Calculations journal May 2006
Predicting Reaction Equilibria for Destabilized Metal Hydride Decomposition Reactions for Reversible Hydrogen Storage journal January 2007
Stability and Reversibility of LiBH 4 journal January 2008

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