U.S. patent application number 13/693158 was filed with the patent office on 2014-06-05 for hydrogen generation from stabilized alane.
This patent application is currently assigned to EVEREADY BATTERY COMPANY, INC.. The applicant listed for this patent is EVEREADY BATTERY COMPANY, INC.. Invention is credited to Guanghong Zheng.
Application Number | 20140154171 13/693158 |
Document ID | / |
Family ID | 48746126 |
Filed Date | 2014-06-05 |
United States Patent
Application |
20140154171 |
Kind Code |
A1 |
Zheng; Guanghong |
June 5, 2014 |
Hydrogen Generation from Stabilized Alane
Abstract
A hydrogen generator and a method of producing hydrogen gas
using stabilized aluminum hydroxide and water are disclosed. The
hydrogen generator contains stabilized aluminum hydride, water, a
base, and a reaction chamber within which at least a portion of the
stabilized aluminum hydride reacts with at least a portion of the
water to produce hydrogen gas. The water that reacts with the
stabilized aluminum hydride is contained in a basic aqueous
solution including at least a portion of the base. The base can be
included with the water in the basic aqueous solution, stored in a
reservoir separate from the stabilized aluminum hydroxide, or the
base can be a solid contained in a mixture with the stabilized
aluminum hydroxide and mix with water when added to the mixture to
form the basic aqueous solution.
Inventors: |
Zheng; Guanghong; (Westlake,
OH) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
EVEREADY BATTERY COMPANY, INC. |
St. Louis |
MO |
US |
|
|
Assignee: |
EVEREADY BATTERY COMPANY,
INC.
St. Louis
MO
|
Family ID: |
48746126 |
Appl. No.: |
13/693158 |
Filed: |
December 4, 2012 |
Current U.S.
Class: |
423/657 ;
422/162 |
Current CPC
Class: |
C01B 3/56 20130101; Y02E
60/362 20130101; C01B 3/065 20130101; Y02E 60/36 20130101; C01B
2203/0405 20130101; B01J 7/02 20130101 |
Class at
Publication: |
423/657 ;
422/162 |
International
Class: |
C01B 3/06 20060101
C01B003/06 |
Claims
1. A method of producing hydrogen gas, the method comprising the
steps of: providing a solid stabilized aluminum hydride, a base and
water; storing the solid stabilized aluminum hydride separate from
the water until production of hydrogen gas is desired; and when the
production of hydrogen gas is desired, contacting at least a
portion of the stabilized aluminum hydride with at least a portion
of the water in a basic aqueous solution comprising at least a
portion of the base to produce hydrogen gas.
2. The method according to claim 1, wherein the stabilized aluminum
hydride comprises alpha aluminum hydride.
3. The method according to claim 1, wherein the stabilized aluminum
hydride comprises particles of aluminum hydride with a crystallite
size of greater than 1 .mu.m.
4. The method according to claim 3, wherein the crystallite size is
100 .mu.m or less.
5. The method according to claim 1, wherein the stabilized aluminum
hydride comprises particles with a passivation layer.
6. The method according to claim 5, wherein the passivation layer
comprises at least one of an oxide of aluminum, a hydroxide of
aluminum and a combination thereof.
7. The method according to claim 1, wherein the basic aqueous
solution is formed by mixing the base and the water and then
contacting the solution with the stabilized aluminum hydride.
8. The method according to claim 7, wherein the basic aqueous
solution is at least a 0.01 molar solution of the base.
9. The method according to claim 1, wherein the basic aqueous
solution is formed as the water is brought in contact with a
mixture of a solid base and stabilized aluminum hydride.
10. The method according to claim 9, wherein the solid base
comprises at least one of a hydride, a borohydride and an alanate
that can initially react with the water to produce hydrogen
gas.
11. The method according to claim 1, wherein no heat is added
during production of the hydrogen gas.
12.-20. (canceled)
21. The method according to claim 1, wherein the solid stabilized
aluminum hydride is stored separate from the base until the
production of hydrogen gas is desired.
22. The method according to claim 1, wherein the solid stabilized
aluminum hydride and the base are stored as a solid mixture before
the production of hydrogen gas is desired.
23. The method according to claim 1, wherein the hydrogen gas is
produced in a reaction area containing all materials required for a
reaction to produce hydrogen gas, and the materials consist
essentially of the aluminum hydride, the base and the water.
24. A method of producing hydrogen gas, the method comprising the
steps of: storing a solid stabilized aluminum hydride and water in
separate containers; and contacting at least a portion of the solid
stabilized aluminum hydride with at least a portion of the water in
the presence of a base to undergo a reaction to produce hydrogen
gas on demand.
25. The method according to claim 24, wherein the base is a solid
stored with the solid stabilized aluminum hydride.
26. The method according to claim 24, wherein the base is stored in
a solution with the water.
27. The method according to claim 24, wherein materials required
for the reaction consist essentially of the stabilized aluminum
hydride, the base and the water.
Description
TECHNICAL FIELD
[0001] This invention relates to the generation of hydrogen gas
from stabilized alane, particularly to the production of hydrogen
gas from the hydrolysis of stabilized alane.
BACKGROUND
[0002] A key limiting factor in the widespread adoption of proton
exchange membrane fuel cell (PEMFC) based power systems is hydrogen
fuel storage. The development of a viable hydrogen storage solution
will have a profound impact on how consumers will power portable
devices, since batteries simply cannot match demands for runtime,
energy density and reliability.
[0003] Because hydrogen has poor energy content per volume (0.01
MJ/L at standard temperature and pressure and 8.4 MJ/L for liquid
hydrogen vs. 32 MJ/L for petroleum), physical transport and storage
as a gas or liquid is impractical. Additionally, the compression
process to achieve the pressures necessary to reach a high density
is energy-intensive and doesn't solve the hazard issue. Also, the
densities of compressed H.sub.2 or liquefied H.sub.2 are still
below those required to reach practical fuel storage goals.
[0004] Physical means to store hydrogen include sorbents such as
carbon nanotubes and foams, zeolites, metal-organic frameworks; and
intermetallics such as titanium-manganese alloy 5800, complex
hydrides such as metal alanates, amides, and borohydrides, and
chemical hydrides such as sodium borohydride/water and ammonia
borane (AB). Despite intensive and elegant work on sorbents and
complex hydrides, practical systems that can store and release
.gtoreq.6 wt % hydrogen at moderate temperatures are still far from
realization.
[0005] Aluminum hydride (alane) is an attractive candidate for
solid hydrogen storage. Alane's formula is sometimes represented
with the formula (AlH.sub.3).sub.n because it is a polymeric
network solid. Alane is formed as numerous polymorphs: the alpha
(.alpha.), alpha prime (.alpha.'), beta (.beta.), delta (.delta.),
epsilon (.epsilon.), zeta (.xi.), or gamma (.gamma.) polymorphs.
Each of the polymorphs has different physical properties and
varying stability. The most thermally stable polymorph is
.alpha.-alane, featuring aluminum atoms surrounded by six hydrogen
atoms that bridge to six other aluminum atoms. However, alane,
including .alpha.-alane, is very reactive with water, including
moisture in ambient air (e.g., see "Right to Know, Hazardous
Substance Fact Sheet" for Aluminum Hydride, available from New
Jersey Department of Health & Senior Services, Right to Know
Program, PO Box 368, Trenton, N.J. 08625-0368;
http://www.nj.gov/health/eoh/rtkweb). For example, It is known that
aluminum hydride reacts violently with oxidizing agents and is not
compatible with strong acids and metal salts), unless it has been
passivated to make it more stable (i.e., stabilized). Consequently,
stabilized alane is generally preferred as a hydrogen containing
material from which hydrogen gas is generated to prevent loss of a
significant portion of the hydrogen from the alane due to wasteful
reactions during manufacturing, shipping and storage. The use of
stabilized alane can also minimize the need for special packaging
and manufacturing under special conditions.
[0006] Alane can react to produce aluminum metal and hydrogen gas
when heated, according to the following reaction:
AlH.sub.3.fwdarw.Al+1.5H.sub.2 (reaction 1)
Alternatively, alane can also react with water according to the
reaction:
AlH.sub.3+3H.sub.2O.fwdarw.Al(OH).sub.3+3H.sub.2 (reaction 2)
However, the hydrolysis of stabilized alane is not normally
effective for producing hydrogen gas at a reasonable rate for most
applications.
[0007] Alane can be prepared by several different processes, such
as those disclosed in U.S. Pat. Nos. 3,852,043; 6,228,338; and
6,617,064. Several different processes for stabilizing or reducing
the reactivity of alane are disclosed in the prior art, such as:
(a) storing in an inert atmosphere below 0.degree. C. for an
extended period of time (U.S. Pat. No. 3,852,043); (b) contacting
with an aqueous buffer at pH 7 at 70.degree. C. (U.S. Pat. No.
3,821,044); (c) treating with a liquid including an organic
compound and a small amount of water (U.S. Pat. No. 3,869,544); and
(d) washing with 10 w/w percent HCl (U.S. Pat. No. 6,228,338 and
U.S. Pat. No. 6,617,064).
[0008] In view of the above, an object of the invention is to
provide a method of producing hydrogen gas at a relatively high
rate by the hydrolysis of stabilized alane.
[0009] Another object of the invention is to provide a hydrogen
generator capable of producing hydrogen gas at a relatively high
rate by the hydrolysis of stabilized alane.
SUMMARY
[0010] The above objects are met and the above disadvantages of the
prior art are overcome by reacting stabilized alane with water in a
basic aqueous solution to produce hydrogen gas.
[0011] One aspect of the present invention is a method of producing
hydrogen gas, the method including the steps of providing
stabilized aluminum hydride, a base and water, and reacting at
least a portion of the stabilized aluminum hydride with at least a
portion of the water to produce hydrogen gas, wherein the water
that reacts with the stabilized aluminum hydride is in a basic
aqueous solution including at least a portion of the base.
Embodiments of the method can include the following, alone or in
combination. [0012] the stabilized aluminum hydride includes alpha
aluminum hydride; [0013] the stabilized aluminum hydride includes
particles of aluminum hydride with a crystallite size having a
D.sub.50 value of greater than 1 .mu.m; the D.sub.50 value can be
100 .mu.m or less; [0014] the stabilized aluminum hydride includes
particles with a passivation layer; the passivation layer can have
a thickness of less than 100 nm; the passivation layer can have a
thickness of at least 1 nm; the passivation layer can include at
least one of an oxide of aluminum, a hydroxide of aluminum and a
combination thereof; [0015] the basic aqueous solution is formed by
mixing the base and the water and then contacting the solution with
the stabilized aluminum hydride; the basic aqueous solution is at
least a 0.01 molar and preferably at least a 0.1 molar solution of
the base; the base can include at least one of sodium hydroxide,
potassium hydroxide, lithium hydroxide, calcium hydroxide, sodium
carbonate, sodium amide and alkyl-lithium; the basic solution can
have a pH of 12 or greater; [0016] the basic aqueous solution is
formed as the water is brought in contact with a mixture of a solid
base and stabilized aluminum hydride; the solid base can be at
least one of a hydroxide, a hydride, a borohydride and an alanate;
the solid base is preferably at least one of a hydride, a
borohydride and an alanate that can initially react with the water
to produce hydrogen gas; [0017] the molar ratio of water to
stabilized aluminum hydride is greater than 3; [0018] the molar
ratio of base to alane is greater than 0.0005; [0019] no heat is
added during production of the hydrogen gas; and [0020] the
reaction of the water and the stabilized aluminum hydride is
capable of producing hydrogen gas at a rate of greater than 1.0
liter of hydrogen gas per kilogam of stabilized aluminum hydride
per hour at without providing additional heat, the reaction of the
water and the stabilized aluminum hydride is preferably capable of
producing up to 100 liters and more preferably up to 500 liters of
hydrogen gas per kilogram of stabilized aluminum hydride per
hour.
[0021] A second aspect of the invention is a hydrogen generator for
producing hydrogen gas, the hydrogen generator including stabilized
aluminum hydride, water, a base, and a reaction chamber within
which at least a portion of the stabilized aluminum hydride reacts
with at least a portion of the water to produce hydrogen gas;
wherein the water that reacts with the stabilized aluminum hydride
is in a basic aqueous solution including and at least a portion of
the base. Embodiments of the hydrogen generator can include the
following, alone or in combination. [0022] the stabilized aluminum
hydride includes alpha aluminum hydride; [0023] the stabilized
aluminum hydride includes particles of aluminum hydride with a
crystallite size having a D.sub.50 value of greater than 1 .mu.m;
the crystallite D.sub.50 value can be 100 .mu.m or less; [0024] the
stabilized aluminum hydride includes particles with a passivation
layer; the passivation layer can have a thickness of less than 100
nm; the passivation layer can have a thickness of at least 1 nm;
the passivation layer can include at least one of an oxide of
aluminum, a hydroxide of aluminum and a combination thereof; [0025]
the water is stored in a reservoir separate from the stabilized
aluminum hydroxide; the water and the base can be part of the basic
solution, and the basic solution can be stored in the reservoir;
the basic aqueous solution can include at least 0.01 molar and
preferably at least 0.1 molar base; the base can include at least
one of sodium hydroxide, potassium hydroxide, lithium hydroxide,
calcium hydroxide, sodium carbonate, sodium amide and
alkyl-lithium; the basic solution can have a pH of 12 or greater;
[0026] the stabilized aluminum hydride and the base are contained
in the hydrogen generator as a solid mixture; the water can be
stored in a separate reservoir; the base can be at least one of a
hydroxide, a hydride, a borohydride and an alanate; the solid base
is preferably at least one of a hydride, a borohydride and an
alanate that can initially react with the water to produce hydrogen
gas; [0027] the molar ratio of water to stabilized aluminum hydride
is greater than 3; [0028] the molar ratio of base to alane is
greater than 0.0005; [0029] the hydrogen generator includes no
heater; [0030] the reaction of the water and the stabilized
aluminum hydride is capable of producing hydrogen gas at a rate of
greater than 1.0 liter of hydrogen gas per kilogram of stabilized
aluminum hydride per hour at without providing additional heat, the
reaction of the water and the stabilized aluminum hydride is
preferably capable of producing up to 100 liters and more
preferably up to 500 liters of hydrogen gas per kilogram of
stabilized aluminum hydride per hour; and [0031] the reaction of
the stabilized aluminum hydroxide with the water is controllable by
controlling transport of the water from a reservoir to the
stabilized aluminum hydroxide to produce hydrogen gas on an as
needed basis.
[0032] These and other features, advantages and objects of the
present invention will be further understood and appreciated by
those skilled in the art by reference to the following
specification, claims and appended drawings.
[0033] Unless otherwise specified, the following definitions and
methods are used herein: [0034] .alpha.-alane (alpha-alane) is
aluminum hydride with a cubic, rhombohedral or hexagonal
morphology; and [0035] stabilized alane is aluminum hydride that is
not classified as a Division 4.3 material for transportation
according to the United Nations "Recommendations of the Transport
of Dangerous Goods, Model Regulations" and the "Globally Harmonized
System of Classification and Labelling of Chemicals (GHS);" in
particular, stabilized alane is aluminum hydride that is not
classified in Division 4.3 if, when tested according to
.sctn.33.4.1.1, Substances which in contact with water emit
flammable gasses, "Recommendations of the Transport of Dangerous
Goods, Manual of Tests and Criteria," the rate of emission of any
hydrogen gas evolved on the test is equal to or less than 1 liter
of hydrogen per kilogram of alane per hour.
[0036] Unless otherwise specified herein, all disclosed
characteristics and ranges are as determined at room temperature
(20-25.degree. C.).
BRIEF DESCRIPTION OF THE DRAWINGS
[0037] In the drawings:
[0038] FIG. 1 is a cross-sectional drawing of an embodiment of a
hydrogen generator;
[0039] FIG. 2 is a graph of cumulative hydrogen volume evolved as a
function of time for stabilized alane in water containing from 0 to
0.51 molar sodium hydroxide; and
[0040] FIG. 3 is a graph of average hydrogen gas evolution rate as
a function of sodium hydroxide concentration during the first hour
of reaction.
DESCRIPTION
[0041] The present invention provides a method of producing
hydrogen gas at a relatively high rate by the hydrolysis of
stabilized alane. A preferred form of alane is .alpha.-alane, which
can have a cubic, rhombohedral or hexagonal morphology. A preferred
stabilized alane has particles or agglomerates of particles having
a passivation layer that renders the alane essentially stable when
in contact with water or moisture in the air. The composition of
the passivation layer can vary, depending on the method of
stabilization. In one embodiment the passivation layer includes one
or a combination of oxides and hydroxides of aluminum (e.g.,
aluminum oxyhydroxide, aluminum hydroxide and aluminum (III)
oxide). Preferably the alane size will have a D.sub.50 value
greater than 1.0 .mu.m. Preferably the D.sub.50 value is no greater
than 100 .mu.m. If the crystallites are too small the total surface
area will be large and the hydrogen gas output will be reduced, and
if the crystallites are too large the particles will be easily
fractured and passivation layers will be broken down during
processing. Preferably the thickness of the passivation layer is
less than 100 nm. Preferably the thickness of the passivation layer
is at least 1 nm. If the passivation layer is too thick the overall
hydrogen content will be reduced and the alane may not react as
desired during use, and if the passivation layer is too thin the
alane will not be as stable as desired.
[0042] Stabilized alane produces little or no hydrogen gas when
exposed to water or to ambient air for up to 24 hours. Test N.5
(described in .sctn.33.4.1.4 of the "Recommendations on the
Transport of Dangerous Goods, Manual of Tests and Criteria," Fifth
revised edition, United Nations, 2009) can be used to determine if
alane is stabilized alane as defined herein. The test method
includes four subtests, the first three to determine if the alane
reacts violently with water or spontaneous ignition of any gas
produced occurs (the first three subtests may be skipped if it is
already known that the alane does reacts violently with water and
spontaneous ignition of any gas produced does not occur. In the
first subtest small quantity (approximately 2 mm diameter) of the
alane to be tested is placed in a trough of distilled water at
20.degree. C.; in the second subtest a small quantity of the alane
(approximately 2 mm diameter) is placed on the center of a filter
paper which is floated flat on the surface of distilled water at
20.degree. C. in a suitable vessel; and in the third subtest alane
is placed in a pile approximately 20 mm high and 30 mm diameter
with a hollow in the top, and a few drops of water are added to the
hollow. For the fourth subtest: [0043] This test should be
performed three times at ambient temperature (20.degree. C.) and
atmospheric pressure. Water is put into the dropping funnel and
enough of the substance (up to a maximum mass of 25 g) to produce
between 100 ml and 250 ml of gas is weighed and placed in a conical
flask. The tap of the dropping funnel is opened to let the water
into the conical flask and a stop watch is started. The volume of
gas evolved is measured by any suitable means. The time taken for
all the gas to be evolved is noted and where possible, intermediate
readings are taken. The rate of evolution of gas is calculated over
7 hours at 1 hour intervals. If the rate of evolution is erratic or
is increasing after 7 hours, the measuring time should be extended
to a maximum time of 5 days. The five day test may be stopped if
the rate of evolution becomes steady or continually decreases and
sufficient data has been established to assign a packing group to
the substance or to determine that the substance should not be
classified in Division 4.3. If the chemical identity of the gas is
unknown, the gas should be tested for flammability. If the alane
tested in the fourth subtest does not react violently with the
water or evolve gas at a rate of greater than 1 liter of hydrogen
per kilogram of alane per hour at any time during the test, and
there is no spontaneous ignition of any gas produced during the
test, the alane is considered to be stabilized alane as defined
herein.
[0044] It is known that the rate of reaction between metal hydrides
and water to produce hydrogen gas can be a function of the pH of
the reaction solution. For example, U.S. Patent Publication No.
2010/0150824 discloses that the hydration reaction typically
proceeds at a faster pace at low pHs, and the addition of an acid
to the reactant may accelerate the evolution of hydrogen gas
(paragraph [0114]); and it may be desirable in some circumstances
to increase the pH to make the composition less reactive and safer
to handle (paragraph [0118]).
[0045] It has been discovered that lowering the pH of a reaction
solution of stabilized alane in water does not substantially
increase the rate of evolution of hydrogen gas. It is believed that
this is because the acid solution does not reduce the passivation
layer on the surface of the alane; in fact, the acid solution may
prevent the disruption of the passivation layer or even add to it.
Contrary to the conventional knowledge that the rate of hydrogen
gas evolution increases with decreasing pH, it has been found that
by making the reaction solution basic the reaction rate of
stabilized alane is increased. It has also been discovered that, at
least to a point, the more base that is added to the water, the
greater the rate of hydrogen gas evolution. Based on the above
discoveries, a method for producing hydrogen gas from stabilized
alane and water has been developed. It includes either mixing a
base with water to form a basic aqueous solution that is then
brought into contact with the stabilized alane or mixing a solid
base with stabilized alane and bringing the water into contact with
the alane/base mixture to form a basic aqueous solution so water
with a high pH can react with the stabilized alane to produce
hydrogen gas.
[0046] Preferably the ratio of water/stabilized alane is greater
than about 3 and more preferably greater than about 5. Preferably
the ratio of water/stabilized alane is no greater than about 20 and
more preferably no greater than about 10. Preferably the molar
ratio of base/stabilized aluminum hydride is greater than about
0.0005 and more preferably greater than about 0.002. to about 0.2,
Preferably the molar ratio of base/stabilized aluminum hydride is
no greater than about 2 and more preferably no greater than about
1.
[0047] When the base is mixed with water in advance, the resultant
basic aqueous solution is preferably at least a 0.01 molar
solution, and more preferably at least a 0.1 molar solution of the
base. Preferably the pH of the solution is at least 12, and more
preferably at least 14.
[0048] Suitable bases will preferably be stable in an aqueous
solution and be soluble in water at the desired concentration and
across the temperature range at which the basic solution is
expected to be used. Preferably the base will have a high
solubility in water, a low molecular weight, and high activity with
the passivation layer of the alane. Suitable bases include
hydroxides (such as those of sodium, potassium, lithium and
calcium), sodium carbonate, sodium amide and alkyl-lithium. If the
base is a solid mixed with the alane, other bases can be used,
including those that can initially react with the water when it is
added to the solid alane/base mixture; examples of such bases
include hydrides (e.g., those of lithium, sodium and potassium),
borohydrides (e.g., those of sodium, lithium, potassium and
calcium), and alanates (e.g., sodium, lithium and potassium
aluminum hydride).
[0049] Preferably the reaction of the water and stabilized alane
will be capable of producing hydrogen gas at a rate of greater than
1.0 liter per kilogram of stabilized alane per hour for at least
short periods of time, though the reaction may be controlled to
produce hydrogen gas at a slower rate or intermittently in order to
provide hydrogen gas only as needed. More preferably the maximum
rate of hydrogen generation will be at least 100 liters per
kilogram, and most preferably at least 500 liters per kilogram of
stabilized alane per hour.
[0050] Stabilized alane can be added to a basic aqueous solution in
a reaction chamber, the basic solution can be added to stabilized
alane in a reaction chamber, or both the basic solution and the
stabilized alane can be added to a reaction chamber. A hydrogen
generator using a basic aqueous solution and stabilized alane as
reactants can use any of these methods. For example, one or both of
the solution and the stabilized alane can be contained in a storage
container and transported to a reaction chamber where the solution
and the stabilized alane come in contact and react to produce
hydrogen gas. In another embodiment, the stabilized alane and water
at a neutral or acidic pH can be present together, with a base
added to the water to raise the pH and cause the water and the
stabilized alane to react. The storage container(s) can be
replaceable or refillable to allow the hydrogen generator to be
recharged with fresh reactants. The reaction chamber can be emptied
or replaced to remove reaction byproducts (e.g., metallic
aluminum). In this way, other components of the hydrogen generator
can be reused, making the hydrogen generator more economical to
use.
[0051] Any suitable means can be used to transport one or more of
the water, base, solution and stabilized alane from a storage
container to the reaction chamber. For example, a liquid (water,
basic solution or liquid base) can be pumped or forced by the
application of pressure on or within the storage container to flow
into the reaction chamber. The stabilized alane can be in a
flowable particulate form (e.g., a dry powder or granular form, or
in a slurry with a liquid slurry). Dry stabilized alane can be
transported using a mechanical device such as a hopper, gravity,
auger or screw feeder. Stabilized alane in a slurry can be
transported by pumping or otherwise flowing under pressure. Because
transporting stabilized alane may be more difficult than
transporting a liquid, it may be desirable to store the stabilized
alane in one or more reaction chambers (or multiple compartments in
the reaction chamber). The generation of hydrogen gas can be
controlled in various ways; e.g., by controlling the rate and
amount of liquid that is transported to the reaction chamber and by
controlling the amount and location of stabilized alane that is
contacted by the basic solution at any given time. A controller can
be used to control the reaction of the water and the stabilized
alane, based on the demand for hydrogen gas from the hydrogen
generator for example.
[0052] A hydrogen generator producing hydrogen gas from the
hydrolysis reaction of water and stabilized alane at a basic pH
will contain a basic aqueous solution and the stabilized alane and
a reaction chamber within which at least a portion of the solution
and the stabilized alane can contact each other and react. The
basic aqueous solution can be provided to the hydrogen generator
(e.g., by filling a storage container or inserting a filled storage
container in the hydrogen generator), or water and a concentrated
base can be provided separately and mixed within the hydrogen
generator. The stabilized alane can be provided by filling or
inserting a storage container or reaction chamber.
[0053] An embodiment of a hydrogen generator is shown in FIG. 1.
The hydrogen generator 10 includes a liquid reservoir 14, a
reaction area 16 and an effluent storage area 18 within a housing
12. Water 20 is contained within the reservoir 14, and stabilized
alane 22 is contained within the reaction area 16. The effluent
storage area 18 includes a filter, which can have one or more
filter components, such as three filter components 24, 26, 28. The
reservoir 14 is enclosed by an enclosure 30. The reaction area 16
can be at least partially enclosed by an optional enclosure 32. The
effluent storage area 18 can be enclosed by an optional enclosure
(not shown). The effluent storage area 18 is in a volume exchanging
relationship with at least one of the reactant storage area 14 and
the reaction area 16. During use of the hydrogen generator 10 the
water 20 is transported from the reactant storage area 14 to the
reaction area 16 through a liquid outlet passage 34 by a pump 54,
preferably located externally. The water 20 can be pumped through
the liquid outlet passage 34, such as a tube, and an outlet
connection 36 to the pump. The water 20 can flow to the reactant
area 16 through a liquid inlet passage 40, such as a tube. The
water 20 exits the liquid inlet passage 40 though a dispersing
member 42 to disperse the water over a larger portion of the
reaction area 16. The stabilized alane 22 can be in a convenient
form such as a pellet, which can include a mixture containing
optional additives. As the water 20 comes in contact with the
stabilized alane 22 they react to produce hydrogen gas. The water
20 can included with a base in a basic aqueous solution stored in
the reservoir 14, or the base can be included in the mixture with
the stabilized alane 22 and dissolve in the water 20 as the water
20 is added to the reaction area. The hydrogen gas flows out of the
reaction area 22 and through an effluent passage to an effluent
entryway 46, where it enters the effluent storage area 18. The
hydrogen gas carries with it effluent that includes reaction
byproducts as well as unreacted water and stabilized alane. The
effluent exits the reaction area 16 though an aperture in the
enclosure 32. The opening in the reaction area enclosure 32 can
include an effluent exit nozzle 44, which can help keep the
aperture open. Hydrogen gas and effluent entering the effluent
storage area 18 through the effluent entryway 46 flows through the
filters 24, 26, 28 toward a distal portion of the effluent storage
area 18. As the hydrogen gas and effluent flow through the filters
24, 26, 28, hydrogen gas is separated from solid particles of the
effluent by the filters 24, 26, 28. The hydrogen gas is separated
from liquids and any remaining solids in the effluent before
exiting the hydrogen generator 10 by a hydrogen permeable, liquid
impermeable material 58. The hydrogen gas flows from the distal
portion of the effluent storage area 18 to the hydrogen outlet
connection 50 through a hydrogen outlet passage 48, from its distal
end 52 to a hydrogen outlet connection 50, where it can exit the
hydrogen generator.
[0054] The following examples illustrate the invention and its
advantages.
Example 1
[0055] Stabilized .alpha.-alane was tested on test N.5, described
above. In subtests 1 to 3, no gas generation or ignition was
observed. In phase 4, 133 mg of stabilized was placed on the bottom
of a 125 cm.sup.3 sidearm (Buchner) flask. About 8 g of distilled
water (enough to flood the stabilized alane sample) was added to
the flask by opening a tap in a dropping funnel that closed the top
of the flask. The tap was immediately closed. An apparatus had been
set up to measure the volume of gas evolved during the test by
water displacement. No evolved gas was observed or measured was
over three days. The fourth subtest was repeated two times with the
same results. This testing confirmed that the alane tested was
stabilized alane as defined herein.
[0056] To the stabilized alane remaining from the first three
subtests was added hydrogen peroxide, sulfuric acid and potassium
hydroxide solution, respectively. The stabilized alane did not
react with the hydrogen peroxide or sulfuric acid, but it did react
with the potassium hydroxide solution as follows. About 9 g of 6.0
molar (27 weight percent) potassium hydroxide solution (pH 15) was
added to the stabilized alane remaining in the sidearm flask at the
end of the three day test. A reaction started immediately when the
potassium hydroxide was added, then the reaction stopped and the
solution became clear after about 10 minutes. A total of 333
cm.sup.3 of evolved gas was measured. The calculated theoretical
amount of hydrogen that would be produced from 133 mg of alane
according to reaction 2 above is 26.87 mg, or 323 cm.sup.3 at
20.degree. C., which is consistent with the measured volume of 333
cm.sup.3, since it was observed that the gas measurement apparatus
had gotten warm during the test as a result of heat produced by the
reaction. This testing showed that the reaction of stabilized alane
and water is not accelerated (or even initiated) with water with a
pH below 7, but that a basic aqueous solution can react with
stabilized alane.
Example 2
[0057] To determine a relationship between stabilized alane and the
pH and concentration of a basic aqueous solution, stabilized
.alpha.-alane was reacted with water at different concentrations of
base to determine the effect of pH of the solution on the rate at
which hydrogen gas is evolved. The test method used was test N.5,
subtest 4, as described above. For each test 10 cm.sup.3 of
deionized water or deionized water containing sodium hydroxide was
added to approximately 150 mg of stabilized .alpha.-alane powder,
measuring the cumulative volume of hydrogen gas evolved during the
test. The results are shown in FIG. 2, in which time in minutes is
on the x-axis and the cumulative volume of hydrogen gas evolved per
gram of stabilized alane is on the y-axis. Line 100 represents the
results with water containing no sodium hydroxide, line 102
represents the results with water containing 0.13 molar (0.5 weight
percent) sodium hydroxide solution (pH 13.0), line 104 represents
the results with water containing 0.25 molar (1.0 weight percent)
sodium hydroxide solution (pH 13.3), line 106 represents the
results with 0.38 molar (1.5 weight percent) sodium hydroxide
solution (pH 13.4), and line 108 represents the results with 0.51
molar (2.0 weight percent) sodium hydroxide solution (pH 13.6).
Stabilized alane immersed in water with no sodium hydroxide for 24
hours produced no measurable amount of hydrogen gas, confirming
that the alane being tested was stabilized alane. Each of the other
samples, in which basic aqueous solution was added to stabilized
alane, evolved hydrogen gas, with the initial rate of hydrogen gas
evolution being greater the higher concentrations of sodium
hydroxide. With a basic solution containing 0.51 molar sodium
hydroxide, essentially all of the stabilized alane reacted (a 100
percent yield) in less than 10 minutes.
[0058] These results show that stabilized alane does not readily
react with water to produce hydrogen gas, but adding at least 0.13
molar sodium hydroxide to the water causes the water and the
stabilized alane to react, and the greater the sodium hydroxide
concentration (up to at least 0.51 molar), the greater the initial
rate of the reaction, and reaction rate levels off such that little
or no additional hydrogen gas is evolved.
[0059] The results are replotted in the graph in FIG. 3 to show the
average hydrogen gas generation rate (in liters of hydrogen gas per
kilogram of stabilized alane per hour) as a function of sodium
hydroxide concentration (in weight percent of solution) during the
first hour on test. This graph shows a significant increase in the
average hydrogen evolution rate as the sodium hydroxide
concentration increases to 1.0 weight percent, but a relatively
small increase in rate from 0.25 to 0.51 molar sodium
hydroxide.
[0060] All references cited herein are expressly incorporated
herein by reference in their entireties. To the extent publications
and patents or patent applications incorporated by reference
contradict the disclosure contained in the present specification,
the present specification is intended to supersede and/or take
precedence over any such contradictory material.
[0061] It will be understood by those who practice the invention
and those skilled in the art that various modifications and
improvements may be made to the invention without departing from
the spirit of the disclosed concept. The scope of protection
afforded is to be determined by the claims and by the breadth of
interpretation allowed by law.
* * * * *
References