CA1061856A - Self-pumping electrochemical cell - Google Patents
Self-pumping electrochemical cellInfo
- Publication number
- CA1061856A CA1061856A CA232,686A CA232686A CA1061856A CA 1061856 A CA1061856 A CA 1061856A CA 232686 A CA232686 A CA 232686A CA 1061856 A CA1061856 A CA 1061856A
- Authority
- CA
- Canada
- Prior art keywords
- cell
- anode
- electrolyte
- cathode
- interior
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000005086 pumping Methods 0.000 title claims abstract description 7
- 239000003792 electrolyte Substances 0.000 claims abstract description 40
- 229910052751 metal Inorganic materials 0.000 claims abstract description 16
- 239000002184 metal Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000012530 fluid Substances 0.000 claims description 3
- 230000001681 protective effect Effects 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- 239000002918 waste heat Substances 0.000 abstract description 3
- 239000002912 waste gas Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 9
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 5
- 229910052744 lithium Inorganic materials 0.000 description 5
- 239000007800 oxidant agent Substances 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000003487 electrochemical reaction Methods 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- 229910013470 LiC1 Inorganic materials 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 1
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000028161 membrane depolarization Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/26—Cells without oxidising active material, e.g. Volta cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/70—Arrangements for stirring or circulating the electrolyte
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Primary Cells (AREA)
Abstract
ABSTRACT
In a reactive metal-water electrochemical cell, a configuration utilizing waste heat and evolved hydrogen gas for pumping electrolyte through the cell. More particularly, the cell is in a vertical, hollow tubular con-figuration with the reactive anode being bonded to the interior surface of the tube casing and a coiled metal screen cathode being positioned within the tubular cell and contacting the anode over essentially its full working sur-face. As the anode is consumed in operation, by reaction with an aqueous electrolyte filling the interior cavity of the tubular configuration, the coil configuration of the cathode forces it to expand and maintain contact with the anode. During operation, evolved waste heat and gas cause a flow of electrolyte through the interior of the cell.
In a reactive metal-water electrochemical cell, a configuration utilizing waste heat and evolved hydrogen gas for pumping electrolyte through the cell. More particularly, the cell is in a vertical, hollow tubular con-figuration with the reactive anode being bonded to the interior surface of the tube casing and a coiled metal screen cathode being positioned within the tubular cell and contacting the anode over essentially its full working sur-face. As the anode is consumed in operation, by reaction with an aqueous electrolyte filling the interior cavity of the tubular configuration, the coil configuration of the cathode forces it to expand and maintain contact with the anode. During operation, evolved waste heat and gas cause a flow of electrolyte through the interior of the cell.
Description
This application describes and claims certain improvements in the basic electrochemical cell disclosed in United States patent 3,791,871.
The basic mechanism of the cell is described in United States pat-ent 3,791,871. Briefly, the cell utilizes a reactive metal anode highly reactive with an aqueous electrolyte and spaced from the cathode by an elec~, trically insulating film which forms naturally on the anode in the presence of water. This thin film permits the cathode to be placed in direct contact with the anode. The resulting reduction in the anode-cathode spacing to a thickness no greater than the thickness of this film greatly reduces the I2R
-` 10 losses which would otherwise be present and results in increased power output and energy density. The anode and cathode operate in an aqueous electrolyte which supports the beneficial electrochemical reaction. The cathode is beneficially formed of an open-mesh metallic screen contoured to contact the anode over substantially the entire operating surface.
~uring operation of the cell, molarity of the electrolyte increases with a resulting decrease in power output. Further, excess heat must be re-moved from the electrolyte which would otherwise result in a loss of effici-ency. Likewise, depolarization of the cell must be accomplished by removal of hydrogen gas evolved at the cathode. Accordingly, the electrolyte is ` 20 normally pumped through the cell in order to remove heat, bring in additional ;; oxidant to maintain desired molarity and remove hydrogen. The use of mech-anical pumps and heat exchangers for this purpose are cumbersome, consume power and generate noise, all of which are undesirable.
This invention relates to a self-pumping reactive metal anode-aqueous electrolyte electrochemical cell consisting essentially of a vertical hollow tubular casing, a reactive anode bonded to the interior surface of said casing, said anode naturally forming on its surface a protective insul-ating film in the presence of water, an expandable coiled metal open-mesh - screen cathode positioned within the interior of said tubular casing and con-tacting said insulating film over substantially all of the anode surface .' ,.. . :
- - :
`` i(~il~S~; :
facing said cathode, said cathode pressing continuously against said insulating film during operation of said cell, an aqueous electrolyte filling the interior cavity of said hollow tubular casing and flowing from the bottom to the top of said cell, and a reservoir containing aqueous electrolyte in fluid communication with the top and bottom of said cell, whereby electrolyte is drawn up through said cell by evolved heat and gas generated during operation of said cell and electrolyte is drawn down through said reservoir as it cools.
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Briefly, in accordance with the invention, there is described a configuration which dispenses with the necessity of mechanical pumps and heat exchangers and, by use of the products of the electrochemical reaction, is self-pumping, the pumping force being supplied by the waste heat and hydrogen gas evolved. The configuration has the further advantage of reduc-ing non-working anode edge surfaces which would normally be exposed to the electrolyte and therefore subject to parasitic erosion.
More particularly, in accordance with the invention, a reactive anode is bonded to the interior surface of a tubular casing and a coiled metal screen cathode is positioned within the casing. The coiled screen presses continuously against the working surface of the anode during the lifetime of the battery. The circular construction of the anode does not provide ~ny non-working exposed edges other than the small top and bottom seams at the ends of the tube and parasitic erosion is accordingly minimized.
- During operation, reaction of the lithium with the electrolyte in the in-terior cavity of the casing causes the electrolyte to be heated thereby establishing a thermal gradient in the cell. This gradient and the buoyancy : .
of the hydrogen gas evolved at the cathode creates a flow of electrolyte through the cell, with hot electrolyte containing hydrogen gas exiting from - 20 the top of the cell and fresh oxidant being drawn into the bottom of the cell.
The various features and advantages of the invention will become apparent upon consideration of the following description taken in conjunction with the accompanying drawing of the preferred embodiment of the invention.
The views of the drawing are as follows:
~ FIGURE 1 is a top view of two self-pumping cells of the invention .- operating from a common reservoir; and ~.
'" -.
. ~
lo~
FIGURE 2 is a edge cross-sectional view of the cells of Figure l.
With reference to Figures 1 and 2, where like reference characters designate corresponding parts throughout the several views, there is depicted two cells of the invention 1 and 2 operating, in this.embodiment, from a com-mon reservoir 3. Reactive metal anodes 4 are bonded, for example by metal-urgical means, to the inside walls of the tubular metal casings 5. me in-sulating film 6 which forms naturally on anodes 4 electrically separates an-odes 4 from expanding coiled metal screen cathodes 7. As the anode 4 is con-sumed in operation, the cathode 7 expands to maintain contact with the anode.
A cathode current collector 8 is bonded to each screen cathode 7 and an an-ode connector 9 is bonded to the exterior of each cell casing 5.
In the embodiment shown in the drawing, two cells l and 2 are con-nected to a central reservoir 3 by means of pipes 10 and 11. me upper pipes 10 are for egress of the circulating electrolyte 12 and the lower pipes ll are for ingress of the electrolyte into the cells. To enhance rejection of heat to the environment the depicted cells and central reservoir may be im_ mersed in a liquid bath such as water. If the liquid bath is an electrically conducting fluid, the exterior surfaces of metal casings ~5) are electrically insulated, for example, with an insulating epoxy paint, not shown. Natur- --ally, there may be only one or more than two cells connected to a central reservoir instead of the two cells depicted in the drawing.
; As the cells operate, the electrolyte 12 circulates down through the reservoir 3 as it cools and evolves the entrained hydrogen and enters the cells 1 and 2 by way of pipes 11. Evolved hydrogen is vented through relief valve 13. Oxidant, norm~lly water, is admitted through inlet pipe 14 as ~e-quired to keep the cells operating at the desired power level.
; As discussed in United States Patent 3,791,871, molarity of the ,::. .
electrolyte is varied to control power output of the ceIls. Whereas conven-- tional batteries decline in both voltage and power during discharge reaching a point of unacceptable low voltage before the active materials are consumedS
'~: ' ' ti voltage and power in the cells of the invention are maintained at the desired level throughout the life of the anode. The voltage and power output per unit area of cel~s of the invention are primarily dependent on electrolyte concen-tration and temperature. The temperature is maintained relatively constant by the configuration of the cells of the invention. Accordingly, control of voltage and power is accomplished by varying the molarity of the electrolyte~
~uring operation, the cells of the invention produce a reactive metal hydrox-ide at the anode which tends to reduce power output as the concentration ex-ceeds in optimum molarity which can be readily calibrated. Accordingly, an oxidant, typically water, is added to the electrolyte to control molarity, that is, reduce the hydroxide concentration~ The control function used to control power output is total cell voltage. Variations of voltage above or below the desired level is sensed by an electronic sensor which actuates a solenoid value which in turn controls the rate of water addition through pipe :. ~
14 to the electrolyte. Excess electrolyte generated by such oxidant additions is vented through valve 13.
Anode 4 is formed of a reactive metal such as sodium or lithium which is highly reacting with and in the presence of water naturally forms on its surface a protective insulating film. Alloys and compounds of such ;
alkali metals and other reac~ive metals should be equally feasible for use as the anode provided they are substantially as reactive with water as are , sodium and lithium and furtherprovided, in common with sodium and lithium, they naturally form a continuous insulating film in the presence of water.
The open-mesh screen cathode is of any suitable electrically conductive material which is non-reactive with water and will permit electrochemical reduction of water during operation of the cell. Illustratively, iron and nickel are preferred materials with black platinum and black nickel provid-ing increased efficiency at the expense of high cost and reduced durability.
The minimum size of the screen is governed by the need to get ., .
.
' ~ ~ : . -,.: ' .
lVt~
electrolyte to the anode face plus the need to remove the products of reaction away from the face. The maxLmum screen si~e is governed by the desire to keep all parts of the anode face as near as possible to the cathode. Illus-tratively, for an anode surface measuring 5 inches by 11 inches, a metal screen- with 0,003 inch metal and 0 1 inch by 0.5 inch openings has produced excellent results.
During operation, the cells of the invention produce a metal hydr_ oxide, the particular metal being dependent on the composition of the anode.
Accordingly, for ease of operation, the aqueous electrolyte is preferably the same as that produced by the reactive metal-water reaction. However, any one of a number of other aqueous solutions sho~ld be equally feasible as a s~art-ing electrolyte provided such electrolytes have the requisite film forming charac~eristics, When dry storage is desired the reservoir 3 may be filled with appropriate dry electrolytes such as lithium hydroxide monohydrate and the cell activated by the introduction of water into the reservoir~
While a central reservoir is not required for single or multiple cell operation, it is considered desirable for multiple cell operation in that the reservoir contributes to maintaining electrical balance between multiple .:. .
-~ cells by providing all cells with electrolyte of equal molarity and temper-ature.
Illustratively, four tubular cells, 6 inches long and 1 inch in diameter, containing 1/8-inch of lithium bonded to the ~nner walls of each ` tube for a length of 52linches, were operated connected to a central reservoir containing 1,0 molar lithium hydroxide solution in LiC1 for two hours at a power level of 50 watts. The temperature of the electrolyte was 28C and the unit was operated in aqueous media at a temperature of 25C, ,...................................................................... :
''~
` .
_ 5 _ . ''~ `~' ' ,
The basic mechanism of the cell is described in United States pat-ent 3,791,871. Briefly, the cell utilizes a reactive metal anode highly reactive with an aqueous electrolyte and spaced from the cathode by an elec~, trically insulating film which forms naturally on the anode in the presence of water. This thin film permits the cathode to be placed in direct contact with the anode. The resulting reduction in the anode-cathode spacing to a thickness no greater than the thickness of this film greatly reduces the I2R
-` 10 losses which would otherwise be present and results in increased power output and energy density. The anode and cathode operate in an aqueous electrolyte which supports the beneficial electrochemical reaction. The cathode is beneficially formed of an open-mesh metallic screen contoured to contact the anode over substantially the entire operating surface.
~uring operation of the cell, molarity of the electrolyte increases with a resulting decrease in power output. Further, excess heat must be re-moved from the electrolyte which would otherwise result in a loss of effici-ency. Likewise, depolarization of the cell must be accomplished by removal of hydrogen gas evolved at the cathode. Accordingly, the electrolyte is ` 20 normally pumped through the cell in order to remove heat, bring in additional ;; oxidant to maintain desired molarity and remove hydrogen. The use of mech-anical pumps and heat exchangers for this purpose are cumbersome, consume power and generate noise, all of which are undesirable.
This invention relates to a self-pumping reactive metal anode-aqueous electrolyte electrochemical cell consisting essentially of a vertical hollow tubular casing, a reactive anode bonded to the interior surface of said casing, said anode naturally forming on its surface a protective insul-ating film in the presence of water, an expandable coiled metal open-mesh - screen cathode positioned within the interior of said tubular casing and con-tacting said insulating film over substantially all of the anode surface .' ,.. . :
- - :
`` i(~il~S~; :
facing said cathode, said cathode pressing continuously against said insulating film during operation of said cell, an aqueous electrolyte filling the interior cavity of said hollow tubular casing and flowing from the bottom to the top of said cell, and a reservoir containing aqueous electrolyte in fluid communication with the top and bottom of said cell, whereby electrolyte is drawn up through said cell by evolved heat and gas generated during operation of said cell and electrolyte is drawn down through said reservoir as it cools.
;, :
: .~
` -.
, . . .
' :
:,, .... .
'.'' .
~:
: . .
`'' .. ,., ~, .
, :
. ..
:, : -la-` .
, " ......... . . . - . :
:~ . . ~ ;.............. .. -l()~ St~
Briefly, in accordance with the invention, there is described a configuration which dispenses with the necessity of mechanical pumps and heat exchangers and, by use of the products of the electrochemical reaction, is self-pumping, the pumping force being supplied by the waste heat and hydrogen gas evolved. The configuration has the further advantage of reduc-ing non-working anode edge surfaces which would normally be exposed to the electrolyte and therefore subject to parasitic erosion.
More particularly, in accordance with the invention, a reactive anode is bonded to the interior surface of a tubular casing and a coiled metal screen cathode is positioned within the casing. The coiled screen presses continuously against the working surface of the anode during the lifetime of the battery. The circular construction of the anode does not provide ~ny non-working exposed edges other than the small top and bottom seams at the ends of the tube and parasitic erosion is accordingly minimized.
- During operation, reaction of the lithium with the electrolyte in the in-terior cavity of the casing causes the electrolyte to be heated thereby establishing a thermal gradient in the cell. This gradient and the buoyancy : .
of the hydrogen gas evolved at the cathode creates a flow of electrolyte through the cell, with hot electrolyte containing hydrogen gas exiting from - 20 the top of the cell and fresh oxidant being drawn into the bottom of the cell.
The various features and advantages of the invention will become apparent upon consideration of the following description taken in conjunction with the accompanying drawing of the preferred embodiment of the invention.
The views of the drawing are as follows:
~ FIGURE 1 is a top view of two self-pumping cells of the invention .- operating from a common reservoir; and ~.
'" -.
. ~
lo~
FIGURE 2 is a edge cross-sectional view of the cells of Figure l.
With reference to Figures 1 and 2, where like reference characters designate corresponding parts throughout the several views, there is depicted two cells of the invention 1 and 2 operating, in this.embodiment, from a com-mon reservoir 3. Reactive metal anodes 4 are bonded, for example by metal-urgical means, to the inside walls of the tubular metal casings 5. me in-sulating film 6 which forms naturally on anodes 4 electrically separates an-odes 4 from expanding coiled metal screen cathodes 7. As the anode 4 is con-sumed in operation, the cathode 7 expands to maintain contact with the anode.
A cathode current collector 8 is bonded to each screen cathode 7 and an an-ode connector 9 is bonded to the exterior of each cell casing 5.
In the embodiment shown in the drawing, two cells l and 2 are con-nected to a central reservoir 3 by means of pipes 10 and 11. me upper pipes 10 are for egress of the circulating electrolyte 12 and the lower pipes ll are for ingress of the electrolyte into the cells. To enhance rejection of heat to the environment the depicted cells and central reservoir may be im_ mersed in a liquid bath such as water. If the liquid bath is an electrically conducting fluid, the exterior surfaces of metal casings ~5) are electrically insulated, for example, with an insulating epoxy paint, not shown. Natur- --ally, there may be only one or more than two cells connected to a central reservoir instead of the two cells depicted in the drawing.
; As the cells operate, the electrolyte 12 circulates down through the reservoir 3 as it cools and evolves the entrained hydrogen and enters the cells 1 and 2 by way of pipes 11. Evolved hydrogen is vented through relief valve 13. Oxidant, norm~lly water, is admitted through inlet pipe 14 as ~e-quired to keep the cells operating at the desired power level.
; As discussed in United States Patent 3,791,871, molarity of the ,::. .
electrolyte is varied to control power output of the ceIls. Whereas conven-- tional batteries decline in both voltage and power during discharge reaching a point of unacceptable low voltage before the active materials are consumedS
'~: ' ' ti voltage and power in the cells of the invention are maintained at the desired level throughout the life of the anode. The voltage and power output per unit area of cel~s of the invention are primarily dependent on electrolyte concen-tration and temperature. The temperature is maintained relatively constant by the configuration of the cells of the invention. Accordingly, control of voltage and power is accomplished by varying the molarity of the electrolyte~
~uring operation, the cells of the invention produce a reactive metal hydrox-ide at the anode which tends to reduce power output as the concentration ex-ceeds in optimum molarity which can be readily calibrated. Accordingly, an oxidant, typically water, is added to the electrolyte to control molarity, that is, reduce the hydroxide concentration~ The control function used to control power output is total cell voltage. Variations of voltage above or below the desired level is sensed by an electronic sensor which actuates a solenoid value which in turn controls the rate of water addition through pipe :. ~
14 to the electrolyte. Excess electrolyte generated by such oxidant additions is vented through valve 13.
Anode 4 is formed of a reactive metal such as sodium or lithium which is highly reacting with and in the presence of water naturally forms on its surface a protective insulating film. Alloys and compounds of such ;
alkali metals and other reac~ive metals should be equally feasible for use as the anode provided they are substantially as reactive with water as are , sodium and lithium and furtherprovided, in common with sodium and lithium, they naturally form a continuous insulating film in the presence of water.
The open-mesh screen cathode is of any suitable electrically conductive material which is non-reactive with water and will permit electrochemical reduction of water during operation of the cell. Illustratively, iron and nickel are preferred materials with black platinum and black nickel provid-ing increased efficiency at the expense of high cost and reduced durability.
The minimum size of the screen is governed by the need to get ., .
.
' ~ ~ : . -,.: ' .
lVt~
electrolyte to the anode face plus the need to remove the products of reaction away from the face. The maxLmum screen si~e is governed by the desire to keep all parts of the anode face as near as possible to the cathode. Illus-tratively, for an anode surface measuring 5 inches by 11 inches, a metal screen- with 0,003 inch metal and 0 1 inch by 0.5 inch openings has produced excellent results.
During operation, the cells of the invention produce a metal hydr_ oxide, the particular metal being dependent on the composition of the anode.
Accordingly, for ease of operation, the aqueous electrolyte is preferably the same as that produced by the reactive metal-water reaction. However, any one of a number of other aqueous solutions sho~ld be equally feasible as a s~art-ing electrolyte provided such electrolytes have the requisite film forming charac~eristics, When dry storage is desired the reservoir 3 may be filled with appropriate dry electrolytes such as lithium hydroxide monohydrate and the cell activated by the introduction of water into the reservoir~
While a central reservoir is not required for single or multiple cell operation, it is considered desirable for multiple cell operation in that the reservoir contributes to maintaining electrical balance between multiple .:. .
-~ cells by providing all cells with electrolyte of equal molarity and temper-ature.
Illustratively, four tubular cells, 6 inches long and 1 inch in diameter, containing 1/8-inch of lithium bonded to the ~nner walls of each ` tube for a length of 52linches, were operated connected to a central reservoir containing 1,0 molar lithium hydroxide solution in LiC1 for two hours at a power level of 50 watts. The temperature of the electrolyte was 28C and the unit was operated in aqueous media at a temperature of 25C, ,...................................................................... :
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Claims (2)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A self-pumping reactive metal anode-aqueous electrolyte electro-chemical cell consisting essentially of a vertical hollow tubular casing, a reactive anode bonded to the interior surface of said casing, said anode naturally forming on its surface a protective insulating film in the presence of water, an expandable coiled metal open-mesh screen cathode positioned within the interior of said tubular casing and contacting said insulating film over substantially all of the anode surface facing said cathode, said cathode pressing continuously against said insulating film during operation of said cell, an aqueous electrolyte filling the interior cavity of said hollow tubular casing and flowing from the bottom to the top of said cell, and a reservoir containing aqueous electrolyte in fluid communication with the top and bottom of said cell, whereby electrolyte is drawn up through said cell by evolved heat and gas generated during operation of said cell and electrolyte is drawn down through said reservoir as it cools.
2. A plurality of electrochemical cells in accordance with claim 1 wherein said cells are connected to a common electrolyte reservoir.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49492974A | 1974-08-05 | 1974-08-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1061856A true CA1061856A (en) | 1979-09-04 |
Family
ID=23966539
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA232,686A Expired CA1061856A (en) | 1974-08-05 | 1975-08-01 | Self-pumping electrochemical cell |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS5924503B2 (en) |
CA (1) | CA1061856A (en) |
DE (1) | DE2530022C2 (en) |
FR (1) | FR2281652A1 (en) |
GB (1) | GB1472516A (en) |
IT (1) | IT1040459B (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3129248A1 (en) * | 1981-07-24 | 1983-02-10 | Accumulatorenwerke Hoppecke Carl Zoellner & Sohn GmbH & Co KG, 5790 Brilon | GALVANIC ELEMENT, IN PARTICULAR METAL AIR CELL |
DE3314174A1 (en) * | 1983-04-19 | 1984-10-25 | Volkswagenwerk Ag, 3180 Wolfsburg | Arrangement for automatic electrolyte circulation |
JPH0592473U (en) * | 1992-05-20 | 1993-12-17 | 川崎重工業株式会社 | Electrical engine cable clamp mechanism for general-purpose engine |
WO2002058171A2 (en) * | 2001-01-22 | 2002-07-25 | Evionyx, Inc. | Electrolyte balance in electrochemical cells |
FR3025055B1 (en) * | 2014-08-19 | 2016-08-26 | Jomi Leman | ELECTROCHEMICAL DEVICE FOR STORING ELECTRIC ENERGY AND HYDROGEN PRODUCTION, AND PROCESS FOR PRODUCING HYDROGEN |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3730776A (en) * | 1970-02-04 | 1973-05-01 | Lockheed Aircraft Corp | Electric current generator and method using consumable alkali metal anode |
US3791871A (en) * | 1971-04-14 | 1974-02-12 | Lockheed Aircraft Corp | Electrochemical cell |
-
1975
- 1975-07-04 DE DE2530022A patent/DE2530022C2/en not_active Expired
- 1975-07-23 JP JP50090014A patent/JPS5924503B2/en not_active Expired
- 1975-07-30 GB GB3188275A patent/GB1472516A/en not_active Expired
- 1975-08-01 CA CA232,686A patent/CA1061856A/en not_active Expired
- 1975-08-04 IT IT26079/75A patent/IT1040459B/en active
- 1975-08-05 FR FR7524442A patent/FR2281652A1/en active Granted
Also Published As
Publication number | Publication date |
---|---|
DE2530022C2 (en) | 1984-07-12 |
DE2530022A1 (en) | 1976-02-19 |
FR2281652A1 (en) | 1976-03-05 |
FR2281652B1 (en) | 1982-03-05 |
JPS5924503B2 (en) | 1984-06-09 |
GB1472516A (en) | 1977-05-04 |
JPS5138033A (en) | 1976-03-30 |
IT1040459B (en) | 1979-12-20 |
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