CA2001346C - Air cell - Google Patents
Air cellInfo
- Publication number
- CA2001346C CA2001346C CA002001346A CA2001346A CA2001346C CA 2001346 C CA2001346 C CA 2001346C CA 002001346 A CA002001346 A CA 002001346A CA 2001346 A CA2001346 A CA 2001346A CA 2001346 C CA2001346 C CA 2001346C
- Authority
- CA
- Canada
- Prior art keywords
- cathode
- anode
- air cell
- present
- current collector
- 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 - Fee Related
Links
- 239000007788 liquid Substances 0.000 claims description 13
- 239000003792 electrolyte Substances 0.000 claims description 7
- 239000005871 repellent Substances 0.000 claims description 5
- 230000003247 decreasing effect Effects 0.000 abstract description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 19
- 239000003208 petroleum Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910000861 Mg alloy Inorganic materials 0.000 description 2
- 229910003307 Ni-Cd Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- -1 polytetrafluoroethylene Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Classifications
-
- 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
Landscapes
- Inert Electrodes (AREA)
- Hybrid Cells (AREA)
Abstract
In an air cell in accordance with the present invention, a current collector (30) is so disposed between an anode (50) and a cathode (20) that it is in contact with the cathode (20), whereby the present invention is very advantageous in that the air cell can be made compact in size and light in weight yet is capable of generating a high output and decreasing the internal resistance. Furthermore, according to the present invention, the cathode (20) is fabricated by assembly a plurality of cathode sections or formed with at least one through hole so that the present invention can provide a cell which is compact in size and light in weight yet is capable of generating a high output.
Description
AIR CELL
BACKGROUND OF THE INVENTION
The present invention relates to an air cell.
In order to drive a motor mounted on a model airplane, one or more cells to be mounted must be compact in size and light in weight so that generally nickel-cadmium cells are used.
For instance, when seven U No. 3 cells (about 170 g) are mounted on a model helicopter, the flight time is of the order of two minutes.
In order to reduce to practical application of such model airplanes to uses such as cropdusting, surveying and photographing, there is a demand for lengthening the flight time. In this case, since the conventional cells have a small output per unit weight and many cells cannot be mounted on a model airplane, the flight time is short.
The conventional cells have a further problem that not only for model helicopters mentioned above but also for driving power supplies which must supply high power, the demands for higher power per unit weight and a longer service life cannot be satisfied.
SUb~iARY OF THE INVENTION
An object of the present invention is to provide an air cell which is compact in size and light in weight yet is capable of supplying a high output.
The air cell in accordance with the present invention is characterized in that a current collector is so disposed between an anode and a cathode that it contacts the cathode.
More specifically, there is provided in one aspect of the invention, an air cell comprising a cathode; an anode having a comb-like shape so that a plurality of openings are defined therethrough; and means for collecting electrons generated at said anode comprising a current collector, the means for collecting electrons contacting the cathode at a surface thereof facing toward the anode.
According to another aspect of the present invention, an air cell comprises a plurality of sections which constitute A
BACKGROUND OF THE INVENTION
The present invention relates to an air cell.
In order to drive a motor mounted on a model airplane, one or more cells to be mounted must be compact in size and light in weight so that generally nickel-cadmium cells are used.
For instance, when seven U No. 3 cells (about 170 g) are mounted on a model helicopter, the flight time is of the order of two minutes.
In order to reduce to practical application of such model airplanes to uses such as cropdusting, surveying and photographing, there is a demand for lengthening the flight time. In this case, since the conventional cells have a small output per unit weight and many cells cannot be mounted on a model airplane, the flight time is short.
The conventional cells have a further problem that not only for model helicopters mentioned above but also for driving power supplies which must supply high power, the demands for higher power per unit weight and a longer service life cannot be satisfied.
SUb~iARY OF THE INVENTION
An object of the present invention is to provide an air cell which is compact in size and light in weight yet is capable of supplying a high output.
The air cell in accordance with the present invention is characterized in that a current collector is so disposed between an anode and a cathode that it contacts the cathode.
More specifically, there is provided in one aspect of the invention, an air cell comprising a cathode; an anode having a comb-like shape so that a plurality of openings are defined therethrough; and means for collecting electrons generated at said anode comprising a current collector, the means for collecting electrons contacting the cathode at a surface thereof facing toward the anode.
According to another aspect of the present invention, an air cell comprises a plurality of sections which constitute A
2 a cathode when assembled together or a cathode is formed with at least one through hole.
As described above, the current collector is so disposed between the anode and the cathode that it contacts the cathode, so that the air cell can be made compact in size and light in weight, has a low degree of internal resistance, and accordingly is advantageous to the generation of a high current.
According to another aspect of the present invention, a cathode is constructed by assembling a plurality of cathode sections or has at least one through hole so that the air cell is compact in size and light in weight yet is capable of producing a high output.
BRIEF DESCRIPTION OF THE DRANINGS
FIG. lA is a longitudinal sectional view of a first embodiment of the present invention;
FIG. 1B is an exploded view illustrating the component parts thereof;
FIG. 2 is a graph indicating the relationship between cathode area and output density;
FIG. 3 illustrates the steps for the fabrication of a cathode 20 in the first embodiment;
FIG. 4 is a graph indicating the relationship between the quantity of active carbon contained in a petroleum-series graphite powder and the output density;
FIG. 5A is a longitudinal sectional view of a second embodiment of the present invention;
FIG. 5B is an exploded view illustrating the component parts thereof;
FIG. 6 is a graph showing discharge curves; and FIG. 7 is a sectional elevation for a description of a third embodiment of the invention.
BEST MODES FOR CARRYING OUT THE INVENTION
FIG. lA is a schematic longitudinal sectional view illustrating the first embodiment of the invention.
FIG. 1B is an exploded view of the right half of the air cell 1 shown in FIG. lA, illustrating its component parts separated from each other.
As described above, the current collector is so disposed between the anode and the cathode that it contacts the cathode, so that the air cell can be made compact in size and light in weight, has a low degree of internal resistance, and accordingly is advantageous to the generation of a high current.
According to another aspect of the present invention, a cathode is constructed by assembling a plurality of cathode sections or has at least one through hole so that the air cell is compact in size and light in weight yet is capable of producing a high output.
BRIEF DESCRIPTION OF THE DRANINGS
FIG. lA is a longitudinal sectional view of a first embodiment of the present invention;
FIG. 1B is an exploded view illustrating the component parts thereof;
FIG. 2 is a graph indicating the relationship between cathode area and output density;
FIG. 3 illustrates the steps for the fabrication of a cathode 20 in the first embodiment;
FIG. 4 is a graph indicating the relationship between the quantity of active carbon contained in a petroleum-series graphite powder and the output density;
FIG. 5A is a longitudinal sectional view of a second embodiment of the present invention;
FIG. 5B is an exploded view illustrating the component parts thereof;
FIG. 6 is a graph showing discharge curves; and FIG. 7 is a sectional elevation for a description of a third embodiment of the invention.
BEST MODES FOR CARRYING OUT THE INVENTION
FIG. lA is a schematic longitudinal sectional view illustrating the first embodiment of the invention.
FIG. 1B is an exploded view of the right half of the air cell 1 shown in FIG. lA, illustrating its component parts separated from each other.
3 The air cell 1 of the first embodiment of the present invention has a glass paper 10, the cathode 20, a current collector 30, a separator 40, an anode 50 and a liquid storage 60 storing therein KC1 liquid 61.
The glass paper 10 is a mounting plate for the cathode 20 and is water repellent.
The cathode 20 is a film mainly consisting of petroleum graphite powder.
As shown in FIG. 1B, the cathode 20 is caused to be in intimate contact with the surface on the side of the anode 50 of the glass paper 10 and is divided into a plurality of sections.
The current collector 30 is in the form of a wire net or a mesh which is fabricated with a metal such as nickel, copper or the like and has a mesh range of from 200 to 300 mesh, so that the air liquid may pass through the current collector 30. It is disposed between the cathode 20 and the anode 50 and is in intimate contact with the cathode 20.
The separator 40 is made of a water absorbing material such as glass paper which has not been subjected to a water repellent treatment. It electrically isolates the current collector 30 from .the anode 50 and absorbs KC1 or NaCl liquid (electrolyte) 61 to be caused by a capillary phenomenon, so that the cathode 20 and the anode 50 are wetted. Instead of glass paper, a sheet of paper can be used for the separator 40.
The anode 50 is made of a magnesium alloy, a zinc alloy, an aluminum alloy or the like. Only one alloy may be used to fabricate the anode 50, or the anode 50 may also be made of a plurality of alloys.
The following chemical reaction takes place at the cathode 20:
X02 + H20 + 2e- -~ 20H~
or 3 5 02 + H20 + 2 e- ~ OZH- + OH-02H- --~ OH- + ~p2
The glass paper 10 is a mounting plate for the cathode 20 and is water repellent.
The cathode 20 is a film mainly consisting of petroleum graphite powder.
As shown in FIG. 1B, the cathode 20 is caused to be in intimate contact with the surface on the side of the anode 50 of the glass paper 10 and is divided into a plurality of sections.
The current collector 30 is in the form of a wire net or a mesh which is fabricated with a metal such as nickel, copper or the like and has a mesh range of from 200 to 300 mesh, so that the air liquid may pass through the current collector 30. It is disposed between the cathode 20 and the anode 50 and is in intimate contact with the cathode 20.
The separator 40 is made of a water absorbing material such as glass paper which has not been subjected to a water repellent treatment. It electrically isolates the current collector 30 from .the anode 50 and absorbs KC1 or NaCl liquid (electrolyte) 61 to be caused by a capillary phenomenon, so that the cathode 20 and the anode 50 are wetted. Instead of glass paper, a sheet of paper can be used for the separator 40.
The anode 50 is made of a magnesium alloy, a zinc alloy, an aluminum alloy or the like. Only one alloy may be used to fabricate the anode 50, or the anode 50 may also be made of a plurality of alloys.
The following chemical reaction takes place at the cathode 20:
X02 + H20 + 2e- -~ 20H~
or 3 5 02 + H20 + 2 e- ~ OZH- + OH-02H- --~ OH- + ~p2
4 On the other hand, when the anode 50 is made of a Mg alloy, the following chemical reactions occur:
Mg + 2 OH- -~ Mg0 + H20 + 2 e-Mg + 2H20 -~ Mg (OH) Z + HZ f (side reaction) The above-described chemical reactions are similar to those of the conventional cells. When a load is connected to the air cell 1, the electron e~ produced in the anode 50 flows through the load and reaches the cathode 20 at which the electron e~ vanishes as described above. In this way, the current flows from the cathode 20 to the anode 50.
In the first embodiment, it is assumed that the cathode 20 is divided into a plurality of cathode sections so that the cathode 20 has flat surface portions 21 and edges 22 which are in contact with the current collector 30. The cathode 20 and the adjacent projections 22 are spaced apart from each other.
Meanwhile, when the quantity of transmitted gas is represented by Q; the coefficient of gas transmission, by P;
the gas pressure difference, by nP; the cross sectional area of the cathode 20, by A' ; the film pressure of the cathode 20, by ~; and the temperature, by t; the following equation (I) is established:
Q = P'(nP/~)'t'A (I) When the gas diffusion coefficient is represented by D; and the solubility by S, the following equation is established:
P - D'S (II) In the first embodiment, the diffusion coefficiency at the edges 22 is greater than that at the flat surface portions 21 of the cathode 20, so that it is seen from the Eq. (II) that the gas transmission coefficient P becomes high at the edges 22 at which the gas diffusion coefficient D is high.
Therefore, from Eq. (I), it is seen that the gas transmission quantity at the edges 22 is greater than that at the flat surface portion. The fact that the gas transmission quantity at each projection 22 is large means that the quantity of the oxygen transmission at each edge 22 is large.
In view of the above, when, instead of fabricating the cathode 20 from a single sheet, the cathode 20 consists . 2001346 of a plurality divided sections, the quantity of the transmitted oxygen becomes large. As a result, the reaction at the cathode which contributes to the power generation is accelerated, so that the generated power is increased.
Mg + 2 OH- -~ Mg0 + H20 + 2 e-Mg + 2H20 -~ Mg (OH) Z + HZ f (side reaction) The above-described chemical reactions are similar to those of the conventional cells. When a load is connected to the air cell 1, the electron e~ produced in the anode 50 flows through the load and reaches the cathode 20 at which the electron e~ vanishes as described above. In this way, the current flows from the cathode 20 to the anode 50.
In the first embodiment, it is assumed that the cathode 20 is divided into a plurality of cathode sections so that the cathode 20 has flat surface portions 21 and edges 22 which are in contact with the current collector 30. The cathode 20 and the adjacent projections 22 are spaced apart from each other.
Meanwhile, when the quantity of transmitted gas is represented by Q; the coefficient of gas transmission, by P;
the gas pressure difference, by nP; the cross sectional area of the cathode 20, by A' ; the film pressure of the cathode 20, by ~; and the temperature, by t; the following equation (I) is established:
Q = P'(nP/~)'t'A (I) When the gas diffusion coefficient is represented by D; and the solubility by S, the following equation is established:
P - D'S (II) In the first embodiment, the diffusion coefficiency at the edges 22 is greater than that at the flat surface portions 21 of the cathode 20, so that it is seen from the Eq. (II) that the gas transmission coefficient P becomes high at the edges 22 at which the gas diffusion coefficient D is high.
Therefore, from Eq. (I), it is seen that the gas transmission quantity at the edges 22 is greater than that at the flat surface portion. The fact that the gas transmission quantity at each projection 22 is large means that the quantity of the oxygen transmission at each edge 22 is large.
In view of the above, when, instead of fabricating the cathode 20 from a single sheet, the cathode 20 consists . 2001346 of a plurality divided sections, the quantity of the transmitted oxygen becomes large. As a result, the reaction at the cathode which contributes to the power generation is accelerated, so that the generated power is increased.
5 Alternatively, when, instead of fabricating the cathode 20 with a plurality of sectioned cathodes, the cathode 20 is made of a single flat sheet and is formed with at least one aperture or through hole, the generated power per unit weight is increased as described above.
In the first embodiment, the current collector 30 is placed in intimate contact with the cathode 20 on the side of the anode 50, so that the electrons generated in the anode 50 need not pass through the cathode 20. As a result, the internal voltage drop in the air cell 1 is less. In the case of a conventional air cell, anodes are disposed at the center portion of an air cell; cathodes are disposed outwardly of the anodes; and a wire net made of a metal such as nickel is disposed outwardly of the cathodes and used as a current collector. In this case, the above-described reactions occur at the cathode side of the anode, or the inner surface of the anode, so that when the electrons flow from the current collectors to the cathodes and further flow through the cathodes, they encounter the electric resistance of the order of 0.1 S2. When a high current of the order of 10 A flows, the voltage drop becomes 1 V.
However, according to the present invention, the current collector 30 is placed in intimate contact with the surface on the side of the anode 50 side of the cathode 20, so that the current collector 30 is disposed at the portion at which the above-mentioned reactions occur, and consequently the electrons generated at the anode 50 can flow directly to the reaction portion without passing through the cathode 20.
Therefore, the internal voltage drop resulting from the passage of electrons through the cathode is decreased. The above-described construction is especially advantageous in the case of flow of a high current.
FIG. 2 illustrates the variation of the output density with variation of the area of the cathode 20.
t~
In the first embodiment, the current collector 30 is placed in intimate contact with the cathode 20 on the side of the anode 50, so that the electrons generated in the anode 50 need not pass through the cathode 20. As a result, the internal voltage drop in the air cell 1 is less. In the case of a conventional air cell, anodes are disposed at the center portion of an air cell; cathodes are disposed outwardly of the anodes; and a wire net made of a metal such as nickel is disposed outwardly of the cathodes and used as a current collector. In this case, the above-described reactions occur at the cathode side of the anode, or the inner surface of the anode, so that when the electrons flow from the current collectors to the cathodes and further flow through the cathodes, they encounter the electric resistance of the order of 0.1 S2. When a high current of the order of 10 A flows, the voltage drop becomes 1 V.
However, according to the present invention, the current collector 30 is placed in intimate contact with the surface on the side of the anode 50 side of the cathode 20, so that the current collector 30 is disposed at the portion at which the above-mentioned reactions occur, and consequently the electrons generated at the anode 50 can flow directly to the reaction portion without passing through the cathode 20.
Therefore, the internal voltage drop resulting from the passage of electrons through the cathode is decreased. The above-described construction is especially advantageous in the case of flow of a high current.
FIG. 2 illustrates the variation of the output density with variation of the area of the cathode 20.
t~
6 The measurement conditions are that the electrolyte is 20s KC1; the film pressure is 180 micrometers; and the temperature is 24°C. It is apparent from FIG. 2 that the output power per unit area when the cathode 20 has a small surface is greater than the output power per unit area when the cathode 20 has a large surface. In the case of FIG. 2, when one cathode 20 has an area of the order of 3 cm2, the maximum power output per unit area can be obtained.
FIG. 3 is a view for a description of the fabrication of a plurality of sections which are assembled together as the cathode 20 as shown in FIG. 1B.
First, the above mentioned petroleum graphite powder and active carbon are mixed in a ratio of about 6:4, and then a polytetrafluoroethylene dispersion liquid is added and mixed. This mixture is a basic material of the cathode 20.
It should be noted here that active carbon is used as a catalyst.
Next, the glass paper 10 which is used as the mounting plate on which is mounted the cathode 20 is subj ected to a water-repellent treatment. Then a mold 60 is mounted on the glass paper 10. Thereafter the basic material of the cathode 20 is cast into the mold 60, and the upper surface of the cast basic material is compressed by a roller.
Next, the basic material of the cathode 20 which is squeezed out of the mold 60 is removed by a scraper, and then the mold 60 is removed. Thereafter the cast basic material of the cathode 20 is heated at a temperature of the order of about 380°C. A plurality of sections of the cathode 20 thus baked are joined to the glass paper 10 as shown in FIG. 1B.
When the mold 60 has a plurality of square openings, the cathode 20 is divided into the form of stripes, so that a high-output air cell can be obtained. Moreover, the mold 60 may be formed with a plurality of openings of a shape other than square such as triangular, pentagonal or round openings.
FIG. 4 indicates the variation of the output density (output power per unit area) with variation in the quantity of the active carbon in the petroleum graphite.
a The test conditions producing the results shown in FIG. 4 are a temperature of 34°C; size of the cathode 20 of cm x 1 cm x 180 micromicrons; quantity of the polytetrafluoroethylene which is diluted four times of four 5 drops (0.2 cc); quantity of water of four drops (0.2 cc); and electrolyte solution (5% NaCl).
The characteristic curve A in FIG. 4 is obtained when petroleum graphite powder A is used. The characteristic curve B is obtained when petroleum graphite powder B is used. The curve B' is obtained when petroleum graphite powder B is subj ected to a treatment with a catalyst . The curve A1 is obtained when petroleum graphite powder A is tested within 20 %
KC1.
As shown in FIG. 4, when the quantity of active carbon is between 30 and 70%, the output power per unit area becomes high. Preferably the quantity of active carbon is between 30 and 50% and, more preferably, between 35 and 45%.
The use of the air cell as an emergency power supply when the performance of the battery mounted on an automotive vehicle drops, as a power supply for a model, or as a power supply for leisure activities such as camping or fishing is very advantageous because the air cell is compact in size, light in weight and capable of generating a high output.
Normally, the cathode 20 and the anode 50 are not placed in contact with the electrolyte such as KC1. When and only when the air cell is used, they are placed in contact with the electrolyte. When the air cell is used in the manner just described above, prior to the use of the air cell, the power drop due to the natural discharge or the like does not occur, so that a long shelf life can be ensured so that the air cell may be used as a power supply in the case of an emergency.
So far it has been described that the electrolyte is KC1, but it is to be understood that sea water, a solution of salt or the like may be equally used.
Instead of the cathode 20 being divided into a plurality of sections as shown in FIG. 1B, the cathode may be in the form of a sheet or plate formed with many pores.
A
FIG. 5A illustrates second embodiment of the present invention. FIG. 5B is an exploded view thereof.
The same reference numerals are used to designate similar parts in the figures.
In the air cell la shown in FIG. 5A, the cathode 20a is in the form of a single flat plate, and the anode 50a is formed with a plurality of through holes 51. Furthermore, only one anode 50a is used.
As described above, the anode plate 50a is formed with a plurality of through holes 51, so that the hydrogen which is produced in the course of the auxiliary reaction when the power is generated can easily separate from the anode 50a.
Then, the reaction speed can be prevented from becoming slow, so that the decrease of the generated power can be decreased.
Furthermore, because of the use of only one anode 50a, the total weight of the air cell la can be decreased.
Furthermore, the anode 50a may be made in the form of a comb enlarging the through holes 51.
FIG. 6 shows the discharge curves of the first and second embodiments in accordance with the present invention and of conventional cells.
In this case, the load resistance is one ohm, and the voltage when the measurements are started is about 1.2 V. It follows therefore that when the output voltage is 1 V, the output current is 1 A.
It is seen from FIG. 6 that in the case of a manganese cell, the output voltage drops below 1 V within a few minutes after the test is started, and in the case of a Ni-Cd cell, the output voltage drops below 1 V within a little over 20 minutes. On the other hand, in the case of the air cell 1 shown in FIG. 1, even though the total weight thereof is only 12 g, and the output voltage drops below 1 V after only 70 minutes. The air cell 50a shown in FIG. 5 drops below 1 V only after 50 minutes even though the total weight of the air cell la is only 12 g.
FIG. 7 illustrates third embodiment of the present invention in which an electrolyte is supplied to a plurality of air cells 1. A plurality of air cells 1 are disposed in a vessel 72, and a tank 70 for storing KC1 liquid 71 is disposed upside down. It follows therefore that as long as the KC1 liquid 71 is stored in the tank 70, it is always supplied to the air cells 1, so that the service life of the air cells is increased. In this third embodiment, more than two tanks 70 can be used, and the air cells 1 may be connected in series or in parallel.
As described above, even though the third embodiment is very light in weight, it can generate high output for a long time. Furthermore, the magnesium used in the above-described examples is contained in sea water and is harmless, and the air cell does not contain any toxic substance such as cadmium used in Ni-Cd cells.
Referring back to FIG. 6, the voltages of the air cells 1 and la are gradually decreased and then increased at some time point. This phenomenon occurs because the KC1 liquid 61 is further supplied. The KC1 liquid 61 evaporates when the air cell is used, so that when the quantity of loss of the KC1 liquid 61 due to its evaporation is replenished, the voltage can be recovered to some extent.
When a plurality of cathodes 20 are fabricated, it is advantageous to carry out the steps shown in FIG. 3 because the fabrication process is simple. Furthermore, the characteristics of the air cell can be stabilized as shown in FIG. 6. The materials used are inexpensive, so that the cost of the air cells can be decreased. Moreover, when the fabrication process as shown in FIG. 3 is used, variations in the quality of the cathodes 20 can be decreased to a minimum.
So far the petroleum graphite powder has been described as being used as a cathode. However, even when a graphite other than petroleum graphite powder is used as a cathode consisting of a plurality of sections, the generated power per unit weight can be increased. Furthermore, even when graphite other than petroleum graphite powder is used as a cathode, the generated power per unit weight can be increased by disposing the current collectors between the anodes on the one hand and the cathodes on the other hand.
The air cell in accordance with the present invention can be used as a power supply cell which must be compact in size and light in weight. For instance, it can be used to drive a model airplane, a power supply in the case of an emergency and so on.
FIG. 3 is a view for a description of the fabrication of a plurality of sections which are assembled together as the cathode 20 as shown in FIG. 1B.
First, the above mentioned petroleum graphite powder and active carbon are mixed in a ratio of about 6:4, and then a polytetrafluoroethylene dispersion liquid is added and mixed. This mixture is a basic material of the cathode 20.
It should be noted here that active carbon is used as a catalyst.
Next, the glass paper 10 which is used as the mounting plate on which is mounted the cathode 20 is subj ected to a water-repellent treatment. Then a mold 60 is mounted on the glass paper 10. Thereafter the basic material of the cathode 20 is cast into the mold 60, and the upper surface of the cast basic material is compressed by a roller.
Next, the basic material of the cathode 20 which is squeezed out of the mold 60 is removed by a scraper, and then the mold 60 is removed. Thereafter the cast basic material of the cathode 20 is heated at a temperature of the order of about 380°C. A plurality of sections of the cathode 20 thus baked are joined to the glass paper 10 as shown in FIG. 1B.
When the mold 60 has a plurality of square openings, the cathode 20 is divided into the form of stripes, so that a high-output air cell can be obtained. Moreover, the mold 60 may be formed with a plurality of openings of a shape other than square such as triangular, pentagonal or round openings.
FIG. 4 indicates the variation of the output density (output power per unit area) with variation in the quantity of the active carbon in the petroleum graphite.
a The test conditions producing the results shown in FIG. 4 are a temperature of 34°C; size of the cathode 20 of cm x 1 cm x 180 micromicrons; quantity of the polytetrafluoroethylene which is diluted four times of four 5 drops (0.2 cc); quantity of water of four drops (0.2 cc); and electrolyte solution (5% NaCl).
The characteristic curve A in FIG. 4 is obtained when petroleum graphite powder A is used. The characteristic curve B is obtained when petroleum graphite powder B is used. The curve B' is obtained when petroleum graphite powder B is subj ected to a treatment with a catalyst . The curve A1 is obtained when petroleum graphite powder A is tested within 20 %
KC1.
As shown in FIG. 4, when the quantity of active carbon is between 30 and 70%, the output power per unit area becomes high. Preferably the quantity of active carbon is between 30 and 50% and, more preferably, between 35 and 45%.
The use of the air cell as an emergency power supply when the performance of the battery mounted on an automotive vehicle drops, as a power supply for a model, or as a power supply for leisure activities such as camping or fishing is very advantageous because the air cell is compact in size, light in weight and capable of generating a high output.
Normally, the cathode 20 and the anode 50 are not placed in contact with the electrolyte such as KC1. When and only when the air cell is used, they are placed in contact with the electrolyte. When the air cell is used in the manner just described above, prior to the use of the air cell, the power drop due to the natural discharge or the like does not occur, so that a long shelf life can be ensured so that the air cell may be used as a power supply in the case of an emergency.
So far it has been described that the electrolyte is KC1, but it is to be understood that sea water, a solution of salt or the like may be equally used.
Instead of the cathode 20 being divided into a plurality of sections as shown in FIG. 1B, the cathode may be in the form of a sheet or plate formed with many pores.
A
FIG. 5A illustrates second embodiment of the present invention. FIG. 5B is an exploded view thereof.
The same reference numerals are used to designate similar parts in the figures.
In the air cell la shown in FIG. 5A, the cathode 20a is in the form of a single flat plate, and the anode 50a is formed with a plurality of through holes 51. Furthermore, only one anode 50a is used.
As described above, the anode plate 50a is formed with a plurality of through holes 51, so that the hydrogen which is produced in the course of the auxiliary reaction when the power is generated can easily separate from the anode 50a.
Then, the reaction speed can be prevented from becoming slow, so that the decrease of the generated power can be decreased.
Furthermore, because of the use of only one anode 50a, the total weight of the air cell la can be decreased.
Furthermore, the anode 50a may be made in the form of a comb enlarging the through holes 51.
FIG. 6 shows the discharge curves of the first and second embodiments in accordance with the present invention and of conventional cells.
In this case, the load resistance is one ohm, and the voltage when the measurements are started is about 1.2 V. It follows therefore that when the output voltage is 1 V, the output current is 1 A.
It is seen from FIG. 6 that in the case of a manganese cell, the output voltage drops below 1 V within a few minutes after the test is started, and in the case of a Ni-Cd cell, the output voltage drops below 1 V within a little over 20 minutes. On the other hand, in the case of the air cell 1 shown in FIG. 1, even though the total weight thereof is only 12 g, and the output voltage drops below 1 V after only 70 minutes. The air cell 50a shown in FIG. 5 drops below 1 V only after 50 minutes even though the total weight of the air cell la is only 12 g.
FIG. 7 illustrates third embodiment of the present invention in which an electrolyte is supplied to a plurality of air cells 1. A plurality of air cells 1 are disposed in a vessel 72, and a tank 70 for storing KC1 liquid 71 is disposed upside down. It follows therefore that as long as the KC1 liquid 71 is stored in the tank 70, it is always supplied to the air cells 1, so that the service life of the air cells is increased. In this third embodiment, more than two tanks 70 can be used, and the air cells 1 may be connected in series or in parallel.
As described above, even though the third embodiment is very light in weight, it can generate high output for a long time. Furthermore, the magnesium used in the above-described examples is contained in sea water and is harmless, and the air cell does not contain any toxic substance such as cadmium used in Ni-Cd cells.
Referring back to FIG. 6, the voltages of the air cells 1 and la are gradually decreased and then increased at some time point. This phenomenon occurs because the KC1 liquid 61 is further supplied. The KC1 liquid 61 evaporates when the air cell is used, so that when the quantity of loss of the KC1 liquid 61 due to its evaporation is replenished, the voltage can be recovered to some extent.
When a plurality of cathodes 20 are fabricated, it is advantageous to carry out the steps shown in FIG. 3 because the fabrication process is simple. Furthermore, the characteristics of the air cell can be stabilized as shown in FIG. 6. The materials used are inexpensive, so that the cost of the air cells can be decreased. Moreover, when the fabrication process as shown in FIG. 3 is used, variations in the quality of the cathodes 20 can be decreased to a minimum.
So far the petroleum graphite powder has been described as being used as a cathode. However, even when a graphite other than petroleum graphite powder is used as a cathode consisting of a plurality of sections, the generated power per unit weight can be increased. Furthermore, even when graphite other than petroleum graphite powder is used as a cathode, the generated power per unit weight can be increased by disposing the current collectors between the anodes on the one hand and the cathodes on the other hand.
The air cell in accordance with the present invention can be used as a power supply cell which must be compact in size and light in weight. For instance, it can be used to drive a model airplane, a power supply in the case of an emergency and so on.
Claims (5)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An air cell comprising a cathode; an anode having a comb-like shape so that a plurality of openings are defined therethrough; and means for collecting electrons generated at said anode, said means comprising a current collector and contacting said cathode at a surface thereof facing toward said anode.
2. An air cell as set forth in claim 1, and further comprising a separator interposed between said cathode and said anode and a reservoir of liquid into which said separator extends, said anode and said cathode being wetted by said liquid via said separator.
3. An air cell as set forth in claim 1, and further comprising a liquid storage means for continuously supplying an electrolyte to said cathode and said anode.
4. An air cell comprising an anode; a cathode having a plurality of spaced-apart sections or at least one through-hole extending therethrough; and a porous water-repellent body to which said cathode is mounted.
5. An air cell as set forth in claim 1, and further comprising a porous water-repellent body to which said cathode is mounted.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CA002001346A CA2001346C (en) | 1989-10-24 | 1989-10-24 | Air cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CA002001346A CA2001346C (en) | 1989-10-24 | 1989-10-24 | Air cell |
Publications (2)
Publication Number | Publication Date |
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CA2001346A1 CA2001346A1 (en) | 1991-04-24 |
CA2001346C true CA2001346C (en) | 1999-12-21 |
Family
ID=4143385
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CA002001346A Expired - Fee Related CA2001346C (en) | 1989-10-24 | 1989-10-24 | Air cell |
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CA (1) | CA2001346C (en) |
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1989
- 1989-10-24 CA CA002001346A patent/CA2001346C/en not_active Expired - Fee Related
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CA2001346A1 (en) | 1991-04-24 |
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