DIRECT SYNTHESIS AND METHODS OF USING HYDROGEN STORAGE MATERIALS

Information

  • Patent Application
  • 20070231254
  • Publication Number
    20070231254
  • Date Filed
    March 30, 2007
    17 years ago
  • Date Published
    October 04, 2007
    17 years ago
Abstract
A method is described for the direct synthesis of reversible hydride materials by hydrogenating a mixture of aluminum, an alkali-metal hydride, and one or more of an alkali-metal amide or an alkali-metal imide, an alkaline-earth-metal or alkaline-earth-metal hydride, and a transition metal catalyst. In one embodiment, the mixture includes aluminum, LiH, LiNH2, magnesium, and TiF3 in the molar ratio of 1:1:2:1:0.05. The material is capable of being repeatedly hydrogenated and dehydrogenated. The method is likely capable of forming a variety of hydrogen storage materials that includes alanates and amides or imides, and which have high hydrogen storage capabilities without the use of ammonia. A method is also described of using two component hydrogen storage materials by segregating the material components.
Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING


FIG. 1 is a graph showing a measurement of hydrogen concentration as a function of time during the first desorption of hydrogen from a mixture;



FIG. 2 is a graph showing a measurement of hydrogen concentration as a function of time during the first absorption of hydrogen from a mixture;



FIG. 3 is a graph showing a measurement of hydrogen concentration as a function of time during the second desorption of hydrogen from a mixture;



FIG. 4 is a graph showing a measurement of hydrogen concentration as a function of time during the third desorption of hydrogen from a mixture;



FIG. 5 as a linear plot of the hydrogen pressure surrounding the material as a function of time;



FIGS. 6 and 7 are a linear plot and log plot, respectively, of the pressure of hydrogen surrounding the material as a function of the hydrogen weight percent in the mixture; and



FIG. 8 is a van't Hoff Plot from PCT isotherm measurements at 250 C, 200 C, and 180 C.


Claims
  • 1. A method for producing compounds capable of reversible hydrogenation, comprising: forming a mixture including an alkali-metal hydride,one or more of an alkali-metal amide or an alkali-metal imide, anda material selected from the group consisting of aluminum, one or more of an alkaline-earth-metal or an alkaline-earth-metal hydride, and any combination thereof, andhydrogenating said mixture at an elevated temperature and elevated hydrogen pressure.
  • 2. The method of claim 1, where said mixture includes a transition metal catalyst.
  • 3. The method of claim 2, where said transition metal catalyst includes a titanium halide.
  • 4. The method of claim 1, where said group includes one or more of an alkaline-earth-metal or an alkaline-earth-metal hydride, and where said one or more of an alkaline-earth-metal or an alkaline-earth-metal hydride includes magnesium.
  • 5. The method of claim 1, where said alkali-metal hydride includes LiH.
  • 6. The method of claim 5, where said group includes aluminum, and where the molar ratio of said aluminum to said LiH is approximately 1:1.
  • 7. The method of claim 1, where said alkali-metal of said alkali-metal hydride, said alkali-metal amide or said alkali-metal imide includes one or more of lithium, sodium, or potassium.
  • 8. The method of claim 1, where said one or more of an alkali-metal amide or an alkali-metal imide includes one or more of lithium amide, sodium amide, or potassium amide.
  • 9. The method of claim 5, where said one or more of an alkali-metal amide or an alkali-metal imide includes LiNH2.
  • 10. The method of claim 9, where the molar ratio of said LiNH2 to said LiH is approximately 2:1.
  • 11. The method of claim 4, where said alkali-metal hydride includes LiH, and where the molar ratio of said Mg to said LiH is approximately 1:1.
  • 12. The method of claim 3, where said titanium halide is TiF3, where said alkali-metal hydride includes LiH, and where the molar ratio of said TiF3 to the LiH is approximately 0.05:1.
  • 13. The method of claim 1, where said group includes aluminum and one or more of an alkaline-earth-metal or an alkaline-earth-metal hydride.
  • 14. The method of claim 1, wherein said step of forming is carried out in an atmosphere consisting essentially of argon.
  • 15. The method of claim 1, wherein said elevated temperature is greater than approximately 200 C.
  • 16. The method of claim 1, wherein said elevated pressure is approximately 125 bar.
  • 17. The method of claim 1, where said mixing includes mixing in a ball mill.
  • 18. A method delivering hydrogen comprising: storing an amide and a complex hydride separately in one or more interconnected vessels;decomposing said amide; andreacting gases from said decomposing amide with said complex hydride to release hydrogen.
  • 19. The method of claim 18, where said complex hydride includes an alanate.
  • 20. The method of claim 19, where said alanate is one or more of a lithium alanate or a sodium alanate.
  • 21. The method of claim 18, where said amide is one or more of a lithium amide or a sodium amide.
  • 22. The method of claim 18, where said gases include ammonia.
Provisional Applications (2)
Number Date Country
60744113 Mar 2006 US
60744934 Apr 2006 US