US3512049A - Electrolytic timer - Google Patents
Electrolytic timer Download PDFInfo
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- US3512049A US3512049A US708970A US3512049DA US3512049A US 3512049 A US3512049 A US 3512049A US 708970 A US708970 A US 708970A US 3512049D A US3512049D A US 3512049DA US 3512049 A US3512049 A US 3512049A
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- 239000010405 anode material Substances 0.000 description 16
- 239000003792 electrolyte Substances 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000000758 substrate Substances 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 5
- 210000005070 sphincter Anatomy 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 150000001879 copper Chemical class 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 229910052715 tantalum Inorganic materials 0.000 description 4
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- RAOSIAYCXKBGFE-UHFFFAOYSA-K [Cu+3].[O-]P([O-])([O-])=O Chemical compound [Cu+3].[O-]P([O-])([O-])=O RAOSIAYCXKBGFE-UHFFFAOYSA-K 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000003915 cell function Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229940116318 copper carbonate Drugs 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- PEVJCYPAFCUXEZ-UHFFFAOYSA-J dicopper;phosphonato phosphate Chemical compound [Cu+2].[Cu+2].[O-]P([O-])(=O)OP([O-])([O-])=O PEVJCYPAFCUXEZ-UHFFFAOYSA-J 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H43/00—Time or time-programme switches providing a choice of time-intervals for executing one or more switching actions and automatically terminating their operations after the programme is completed
- H01H43/32—Time or time-programme switches providing a choice of time-intervals for executing one or more switching actions and automatically terminating their operations after the programme is completed with timing of actuation of contacts due to electrolytic processes; with timing of actuation of contacts due to chemical processes
Definitions
- a Well designed cell will have (under given conditions as to temperature, applied voltage, etc.), a sub stantially constant resistance while the anodic material is plating and a higher resistance thereafter. In between, the resistance may rise due to partial removal of anodic material producing partial exposure of substrate, followed by a further rise as the anodic ions remaining in the electrolyte are cleared out, following the complete exhaustion of the anodic material from the anode itself.
- the result of such transitional phenomena is to lessen the sharpness of the resistance change and hence to increase possible error in the precise time of operation of the cell.
- the invention in its broader aspect is applicable to visual indicating cells and to cells adapted to measuring the elapsed time, as distinguished from those which merely indicate the end of a predetermined interval, its advantages are realized most fully in miniature, one-shot, electrically operating cells, and it is an object of the invention to provide a cell structure and operation which permit the production of such cells economically and with a high degree of reliability and accuracy.
- FIG. 1 is a schematic simplified circuit diagram
- FIG. 2 is an operating curve
- FIG. 3 is an axial section, taken on line iii-iii of FIG. 4, of the cell of the invention
- FIGS. 4 and 5 are, respectively, an end elevation and section on the line v-v of FIG. 3;
- FIGS. 6 and 7 are, respectively, an axial section and section on the line vii-vii thereof, of a modification.
- FIGS. 8 and 9 are, respectively, a view partly in central axial section and partly in elevation and a section on the line viivii, showing the cell of FIGS. 6 and 7 after plating of the anodic material.
- the leads 11, 17 of the timing cell are shown as connected through a voltage dropping resistor 2 to an indicated by the battery 1.
- a meter 3 reads the voltage across the cell. So long as the cell has not consumed a predetermined quantity of anodic material, the voltage across it will remain at a substantially constant low value (V0 in FIG. 2), which voltage will be the voltage across the source 1 less the voltage across resistor 2 (IXR). Once the anodic material is exhausted, the current drops, as also the voltage drop across resistor 2, so that the voltage across the cell rises and may approximate that of the source 1.
- the permissible stopped voltage across the cell cannot be permitted, in many applications, to remain for any length of time above the value at Which dissociation of the electrolyte and gas formation occur. This value is ordinarily about 0.7 volt, or less.
- Cells, as heretofore constructed with an insoluble (e.g., gold plated) substrate supporting the anodic material still have a fairly low resistance, corresponding to a voltage drop such as indicated by the dot-dash line Vs in FIG. 2, and a comparatively gradual transition from the operating voltage drop- V0.
- a cell constructed according to the present invention may have a very much increased Stopped voltage Vs and much sharper transition.
- the envelope or casing 10 is preferably formed from conductive metal (e.g., copper), and serves as the cathode, being provided with a lead 11 for connecting the cell to another conductor or circuit element.
- the anodic member 12 of the cell has a radial flange 13 for securing and sealing it into the cell envelope 10. As shown in FIG. 3, the flange periphery is held in position axially and radially, and in spaced relation to the wall of the envelope 10 by means of a pair of O-rings 14, which are compressed against the flange 13 and inside of the wall of envelope 10 by the narrowed neck 15 and turned in rim 16 of the envelope 10.
- the manufacture of the member 10 and its assembly with anodic member 12 involve only standard and economical mass production procedures.
- Anode 12 has a connecting lead 17 and extends into the envelope 10 as indicated at 18.
- anodic material 19 e.g., copper
- the portion of the anode member section 18 and flange 13 which are not covered by the anodic material 19 may be passivated so as to be rendered non-conductive or may be coated with a non-conductive varnish.
- the anodic member 12 generally is conductive, apart from its surface wherever passivated or coated with insulating material, and the voltage drop across the interface between section 18 and the anodic material 19 is negligible.
- the material of the anodic member, or at least the surface of section 18 thereof, is such, however, that as the section 18 is exposed to the electrolyte by removal of anodic material 19, its surface is passivated and forms a high resistance coating which also resists further attack by the electrolyte.
- the anode may be formed of a variety of metals, including aluminum, tantalum and titanium, tantalum being the preferred metal for use as the anodic member or substrate in the cell of the invention.
- the tantalum is first formed into the shape shown, and the part of the extension 18 which is to be covered by the anodic material 19 is then scraped, ground or abraded to remove the surface oxide layer, while submerged in an inert fluid such as alcohol or in an inert atmosphere. While still protected by an adhering layer of the alcohol or by other inert fluid or gas, the member is made the cathode of a plating bath and has a predetermined quantity of the anodic material plated onto it, this being accomplished before any substantial reformation of oxide coating can occur.
- the anodic material thus plated onto the anodic member is preferably copper, as also is the cathode member of the timing cell.
- a suitable electrolyte (E in FIG. 3) may consist of water, phosphoric acid and a copper salt.
- the phosphoric acid content of the electrolyte exceeds 50% concentration and the copper salt may be copper phosphate, copper pyrophosphate or copper carbonate.
- the electrolyte solution may be prepared by heating the phosphoric acid solution to 75 C. and dissolving the copper salt in it. Copper metal is then added and the solution is maintained at 75 C. until no more copper dissolves. After filtering, it is ready for use.
- the cell of the invention may be made with a glass or other transparent envelope, and may also be arranged for reading the elapse time at intermediate values, in addition to the terminal value.
- the cell construction and proportions may also be varied, as well as the manner of connecting it into a circuit, as by substituting for the wire leads 11, 17 prongs adapted to be plugged in suitable spring sockets.
- the preferred form, however, is generally as described above, utilizing a drawn or extruded cathode which also serves as the container for the electrolyte.
- the size of the cell is also varied to suit the requirements of particular applications, but a cell having a diameter of about one quarter inch will be found suitable for a wide variety of uses.
- One typical use for the cell is as a switching device, a transistor or relay being substituted for the meter 3 of 'FIG. 1.
- the cell when the controlled operation has continued for a predetermined time the cell functions to switch off the power, thus terminating the operation, or may switch over so as to initiate another operation.
- the circuit may be arranged so as to measure a chronological time interval or so as to measure the time integral of any desired quantity. Missiles, satellites, detonating devices and automatic equipment of a great many kinds involve uses of this type.
- the cell affords improved accuracy and also permits uses where it is left in place indefinitely in the stopped condition, due to its high stopped resistance and a consequent ability to take high stopped voltages without causing dissociation of the electrolyte and accompanying production of gas.
- the cell may be connected to the wiring of a motor vehicle or appliance of various kinds, the object being to measure either the lapse of a given period of operating time or the integral of a quantity representing rate of use.
- the cell may be connected through a dropping resistor to the battery of a car, whenever the car switch is turned on to a driving position. The cell will then indicate the expiration of a predetermined number of driving hours, which may be made the expiration period for a guarantee.
- the cell may also be connected to read a voltage proportional to speed of the engine or vehicle, thus providing fora guarantee period which depends upon the operating speed. In a particular case where the proportionality is direct, the interval measured will, of course, be the distance driven.
- the running out of the allotted time or service period may operate any desired signal or switch device, and, in cases such as just mentioned, may take place without any obvious indication whatsoever, the cell remaining in place unless and until a check on the service period is required, and this is readily accomplished by reading the cell resistance. If no such reading is required, the cell may remain in place indefinitely and require no provision to protect against gas production, even though subjected to a comparatively high voltage, as, for example, several volts in the automobile use discussed above.
- the cell of the invention is adapted to withstanding severe shock and vibration conditions, as required in many missile and other applications, and is also adapted to use over a wide temperature range, such as from 5S C. to +71 C.
- the cell can be made in convenient capacities, such as, for example, one, five, twenty or fifty hundred microampere hours, (0.0001, 0.0005, 0.0020 or 0.0050 ampere hour), and stored and used as required, a shelf life in excess of ten years being obtainable.
- FIGS. 6 to 10 show a modified form of the invention.
- the anode element 27-28 may be composed entirely of the platable material, such as copper, and is supported in an inert plastic member 21 which insulates most of the anode from the cathodic shell 10 and from the electrolyte E therein.
- Member 21 may be made of Teflon, polyethylene, or any other plastic having suitable mechanical and electrical properties.
- Member 21 is held and sealed in casing 10 by the enlarged section or flange 22 and has a shaft 23 extending into the interior of the cell and having a hollow center 24.
- the anode 27 passes through member 21, fitting in sealing relation to the passage 26 at one end of the space 24 and to the sphincter 25 (needle hole or slit) at the other end thereof.
- Anode 27 preferably terminates in an enlarged end 28 containing most of the metal to be plated.
- the space 24 may be filled with an inert material such as a silicone oil or grease, which may ooze out slightly, forming a bead 29 which assists in insulating the space 24 and anode 27 from the'electrolyte E, thereby producing an effect similar to the coating formation in the embodiment of FIGS. 3 to 5.
- an inert material such as a silicone oil or grease
- a sealed coulometer timer cell comprising a cathode, an anodic element and an electrolyte. contacting the cathode and anodic element, a quantity of material selectively platable electrolytically on either said cathode or anodic element, and means operable upon deplating a predetermined part of said material from the anodic element for covering the surface exposed thereby with an electrically insulating layer.
- a sealed coulometer timer cell in which the anodic element comprises a substrate of conductive metal and said quantity of material comprises a predetermined amount of a different metal carried on said substrate, and the said substrate metal reacts with the electrolyte to form an anodized electrically insulating surface layer, whereby exposure of'the substrate by deplating the said different metal results in the formation of said layer.
- a sealed coulometer timer cell in which the anodic element comprises a shaft and a sphincter of insulating material surrounding the same in sealed relation thereto, the said predetermined part of said material being immersed in the electrolyte and adjacent the sphincter, whereby deplating thereof permits closing of the sphincter to cover the remainder of the anodic element.
Landscapes
- Electroplating And Plating Baths Therefor (AREA)
Description
May 12, 1970 M. HOBERMAN' ET L 3,
ELECTROLYTIC TIMER Filed Feb. 28, 1968 INVENTORS BY WWW United States Patent 3,512,049 ELECTROLYTIC TIMER Max Hoberman, Teaneck, and Marshall Leibowitz, Englewootl, N.J., assignors to Bergen Laboratories, Inc., Paterson, N..l., a corporation of New Jersey Filed Feb. 28, 1968, Ser. No. 708,970 Int. Cl. H01g 9/00 US. Cl. 317230 4 Claims ABSTRACT OF THE DISCLOSURE This invention relates to electrolytic timing cells or coulometers, and more particularly to such cells in which elapsed time is measured by the plating of an anodic material.
One of the early uses of such devices was in the acceleration integrator of the German V-2 missile, in which the depletion of anodic silver chloride produced a cell functioning as a battery to produce an which signaled the occurrence of the condition to be sensed by the cell. In the nature of the case, the behavior of the cell thereafter was of but little interest. In later electrolytic timers, where the cell might remain in circuit after exhaustion of the predetermined quantity of anodic material, it has been found important to produce a large rise in the voltage drop across the cell in order to activate voltage operated auxiliary devices.
A Well designed cell will have (under given conditions as to temperature, applied voltage, etc.), a sub stantially constant resistance while the anodic material is plating and a higher resistance thereafter. In between, the resistance may rise due to partial removal of anodic material producing partial exposure of substrate, followed by a further rise as the anodic ions remaining in the electrolyte are cleared out, following the complete exhaustion of the anodic material from the anode itself. The result of such transitional phenomena is to lessen the sharpness of the resistance change and hence to increase possible error in the precise time of operation of the cell.
It is an object of the invention to lessen the transition time and increase the magnitude of the change of resistance and thereby increase the accuracy of the cell.
While the invention in its broader aspect is applicable to visual indicating cells and to cells adapted to measuring the elapsed time, as distinguished from those which merely indicate the end of a predetermined interval, its advantages are realized most fully in miniature, one-shot, electrically operating cells, and it is an object of the invention to provide a cell structure and operation which permit the production of such cells economically and with a high degree of reliability and accuracy.
With the foregoing objects in mind, as well as others which will appear in the course of the following description, the invention will now first be described with reference to a preferred embodiment, as illustrated in the accompanying drawing, and the features forming the invention will then be pointed out in the appended claims.
In the drawing:
FIG. 1 is a schematic simplified circuit diagram;
FIG. 2 is an operating curve;
FIG. 3 is an axial section, taken on line iii-iii of FIG. 4, of the cell of the invention;
3,512,049 Patented May 12, 1970 FIGS. 4 and 5 are, respectively, an end elevation and section on the line v-v of FIG. 3;
FIGS. 6 and 7 are, respectively, an axial section and section on the line vii-vii thereof, of a modification; and
FIGS. 8 and 9 are, respectively, a view partly in central axial section and partly in elevation and a section on the line viivii, showing the cell of FIGS. 6 and 7 after plating of the anodic material.
Referring now to FIG. 1, the leads 11, 17 of the timing cell (casing 10) are shown as connected through a voltage dropping resistor 2 to an indicated by the battery 1. A meter 3 reads the voltage across the cell. So long as the cell has not consumed a predetermined quantity of anodic material, the voltage across it will remain at a substantially constant low value (V0 in FIG. 2), which voltage will be the voltage across the source 1 less the voltage across resistor 2 (IXR). Once the anodic material is exhausted, the current drops, as also the voltage drop across resistor 2, so that the voltage across the cell rises and may approximate that of the source 1. However, the permissible stopped voltage across the cell cannot be permitted, in many applications, to remain for any length of time above the value at Which dissociation of the electrolyte and gas formation occur. This value is ordinarily about 0.7 volt, or less. Cells, as heretofore constructed with an insoluble (e.g., gold plated) substrate supporting the anodic material still have a fairly low resistance, corresponding to a voltage drop such as indicated by the dot-dash line Vs in FIG. 2, and a comparatively gradual transition from the operating voltage drop- V0. A cell constructed according to the present invention may have a very much increased Stopped voltage Vs and much sharper transition.
A preferred type of cell is shown by Way of example in FIGS. 1 to 3. The envelope or casing 10 is preferably formed from conductive metal (e.g., copper), and serves as the cathode, being provided with a lead 11 for connecting the cell to another conductor or circuit element. The anodic member 12 of the cell has a radial flange 13 for securing and sealing it into the cell envelope 10. As shown in FIG. 3, the flange periphery is held in position axially and radially, and in spaced relation to the wall of the envelope 10 by means of a pair of O-rings 14, which are compressed against the flange 13 and inside of the wall of envelope 10 by the narrowed neck 15 and turned in rim 16 of the envelope 10. As will be apparent to those skilled in the art, the manufacture of the member 10 and its assembly with anodic member 12 involve only standard and economical mass production procedures.
The anodic member 12 generally is conductive, apart from its surface wherever passivated or coated with insulating material, and the voltage drop across the interface between section 18 and the anodic material 19 is negligible. The material of the anodic member, or at least the surface of section 18 thereof, is such, however, that as the section 18 is exposed to the electrolyte by removal of anodic material 19, its surface is passivated and forms a high resistance coating which also resists further attack by the electrolyte. The anode may be formed of a variety of metals, including aluminum, tantalum and titanium, tantalum being the preferred metal for use as the anodic member or substrate in the cell of the invention. In any case, exposure of the substrate metal to the electrolyte will anodize the metal, producing an electrically insulating surface thereon, which inhibits any further current flow through the cell. In making the anodic member, the tantalum is first formed into the shape shown, and the part of the extension 18 which is to be covered by the anodic material 19 is then scraped, ground or abraded to remove the surface oxide layer, while submerged in an inert fluid such as alcohol or in an inert atmosphere. While still protected by an adhering layer of the alcohol or by other inert fluid or gas, the member is made the cathode of a plating bath and has a predetermined quantity of the anodic material plated onto it, this being accomplished before any substantial reformation of oxide coating can occur.
The anodic material thus plated onto the anodic member is preferably copper, as also is the cathode member of the timing cell. A suitable electrolyte (E in FIG. 3) may consist of water, phosphoric acid and a copper salt. The phosphoric acid content of the electrolyte exceeds 50% concentration and the copper salt may be copper phosphate, copper pyrophosphate or copper carbonate. the electrolyte solution may be prepared by heating the phosphoric acid solution to 75 C. and dissolving the copper salt in it. Copper metal is then added and the solution is maintained at 75 C. until no more copper dissolves. After filtering, it is ready for use.
The cell of the invention may be made with a glass or other transparent envelope, and may also be arranged for reading the elapse time at intermediate values, in addition to the terminal value. The cell construction and proportions may also be varied, as well as the manner of connecting it into a circuit, as by substituting for the wire leads 11, 17 prongs adapted to be plugged in suitable spring sockets. The preferred form, however, is generally as described above, utilizing a drawn or extruded cathode which also serves as the container for the electrolyte. The size of the cell is also varied to suit the requirements of particular applications, but a cell having a diameter of about one quarter inch will be found suitable for a wide variety of uses.
One typical use for the cell is as a switching device, a transistor or relay being substituted for the meter 3 of 'FIG. 1. In this case, when the controlled operation has continued for a predetermined time the cell functions to switch off the power, thus terminating the operation, or may switch over so as to initiate another operation.
Another typical use of the cell is toindicate an expiration of predetermined operating time, and in this case, a neon lamp may be substituted for the meter 3 of FIG. 1. The circuit may be arranged so as to measure a chronological time interval or so as to measure the time integral of any desired quantity. Missiles, satellites, detonating devices and automatic equipment of a great many kinds involve uses of this type. The cell affords improved accuracy and also permits uses where it is left in place indefinitely in the stopped condition, due to its high stopped resistance and a consequent ability to take high stopped voltages without causing dissociation of the electrolyte and accompanying production of gas.
Another use for the cell is the measurement of the lapse of guaranteed operating time. For example, the cell may be connected to the wiring of a motor vehicle or appliance of various kinds, the object being to measure either the lapse of a given period of operating time or the integral of a quantity representing rate of use. Thus, the cell may be connected through a dropping resistor to the battery of a car, whenever the car switch is turned on to a driving position. The cell will then indicate the expiration of a predetermined number of driving hours, which may be made the expiration period for a guarantee. The cell may also be connected to read a voltage proportional to speed of the engine or vehicle, thus providing fora guarantee period which depends upon the operating speed. In a particular case where the proportionality is direct, the interval measured will, of course, be the distance driven. The running out of the allotted time or service period may operate any desired signal or switch device, and, in cases such as just mentioned, may take place without any obvious indication whatsoever, the cell remaining in place unless and until a check on the service period is required, and this is readily accomplished by reading the cell resistance. If no such reading is required, the cell may remain in place indefinitely and require no provision to protect against gas production, even though subjected to a comparatively high voltage, as, for example, several volts in the automobile use discussed above.
The cell of the invention is adapted to withstanding severe shock and vibration conditions, as required in many missile and other applications, and is also adapted to use over a wide temperature range, such as from 5S C. to +71 C. The cell can be made in convenient capacities, such as, for example, one, five, twenty or fifty hundred microampere hours, (0.0001, 0.0005, 0.0020 or 0.0050 ampere hour), and stored and used as required, a shelf life in excess of ten years being obtainable.
FIGS. 6 to 10 show a modified form of the invention. In this form, the anode element 27-28 may be composed entirely of the platable material, such as copper, and is supported in an inert plastic member 21 which insulates most of the anode from the cathodic shell 10 and from the electrolyte E therein. Member 21 may be made of Teflon, polyethylene, or any other plastic having suitable mechanical and electrical properties. Member 21 is held and sealed in casing 10 by the enlarged section or flange 22 and has a shaft 23 extending into the interior of the cell and having a hollow center 24. The anode 27 passes through member 21, fitting in sealing relation to the passage 26 at one end of the space 24 and to the sphincter 25 (needle hole or slit) at the other end thereof. Anode 27 preferably terminates in an enlarged end 28 containing most of the metal to be plated. When the anode has been plated away so as to remove the enlargement 28, the sphincter 25 is permitted to close around the end of the remaining part of anode 27, insulating against further current flow. The space 24 may be filled with an inert material such as a silicone oil or grease, which may ooze out slightly, forming a bead 29 which assists in insulating the space 24 and anode 27 from the'electrolyte E, thereby producing an effect similar to the coating formation in the embodiment of FIGS. 3 to 5.
What is claimed is: v
1. A sealed coulometer timer cell comprising a cathode, an anodic element and an electrolyte. contacting the cathode and anodic element, a quantity of material selectively platable electrolytically on either said cathode or anodic element, and means operable upon deplating a predetermined part of said material from the anodic element for covering the surface exposed thereby with an electrically insulating layer.
2. A sealed coulometer timer cell according to claim 1, in which the anodic element comprises a substrate of conductive metal and said quantity of material comprises a predetermined amount of a different metal carried on said substrate, and the said substrate metal reacts with the electrolyte to form an anodized electrically insulating surface layer, whereby exposure of'the substrate by deplating the said different metal results in the formation of said layer.
3. A sealed coulometer timer cell according to claim 2, in which the substrate is tantalum, the said different metal is copper and the electrolyte is composed of phosphoric acid and a copper salt. 0
4. A sealed coulometer timer cell according to claim 1, in which the anodic element comprises a shaft and a sphincter of insulating material surrounding the same in sealed relation thereto, the said predetermined part of said material being immersed in the electrolyte and adjacent the sphincter, whereby deplating thereof permits closing of the sphincter to cover the remainder of the anodic element.
References Cited UNITED STATES PATENTS 6 3,210,662 10/ 1965 Steinmetz et a1. 324-94 3,423,644 1/ 1969 Mintz 317--23 1 3,423,648 1/1969 Mintz 'a. 317-23l JAMES D. KALLAM, Primary Examiner US. Cl. X.R.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US70897068A | 1968-02-28 | 1968-02-28 |
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US3512049A true US3512049A (en) | 1970-05-12 |
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Application Number | Title | Priority Date | Filing Date |
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US708970A Expired - Lifetime US3512049A (en) | 1968-02-28 | 1968-02-28 | Electrolytic timer |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3564347A (en) * | 1969-01-21 | 1971-02-16 | Sprague Electric Co | Electrochemical timer |
US3679945A (en) * | 1969-09-20 | 1972-07-25 | Matsushita Electric Ind Co Ltd | Electric quantity memory element |
US3700974A (en) * | 1971-11-10 | 1972-10-24 | Edward J Plehal | Electrolytic cell with inner electrode having non-reactive surface |
US3949279A (en) * | 1971-11-12 | 1976-04-06 | P. R. Mallory & Co., Inc. | Recessed anode with particulate metal deposit |
US3956676A (en) * | 1973-11-02 | 1976-05-11 | P. R. Mallory & Co., Inc. | Electrical device having anode riser assembly with polymeric film means |
US4164066A (en) * | 1971-11-12 | 1979-08-14 | P. R. Mallory & Co., Inc. | Fabrication of anodes by plasma spray deposition |
US20130163392A1 (en) * | 2011-12-23 | 2013-06-27 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9164493B2 (en) | 2001-12-13 | 2015-10-20 | Vision Works Ip Corporation | Time dependent-temperature independent color changing label |
US9188962B2 (en) | 2011-11-01 | 2015-11-17 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9606512B2 (en) | 2002-12-13 | 2017-03-28 | Vision Works Ip Corporation | Environment dependent—temperature independent color changing label |
US9632485B2 (en) | 2002-12-13 | 2017-04-25 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US10318604B2 (en) | 2017-02-13 | 2019-06-11 | Vision Works Ip Corporation | Electronically readable system and device with changing codes |
US10338537B2 (en) | 2014-09-08 | 2019-07-02 | Vision Works Ip Corporation | Indicators for external variables consisting of singular and multiple depletion cells |
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US3210662A (en) * | 1961-07-20 | 1965-10-05 | United Nuclear Corp | Electrolytic indicator with an electrode having a thin frangible coating thereon |
US3423648A (en) * | 1966-01-10 | 1969-01-21 | Bissett Berman Corp | Electrolytic cell with electrically conductive masking surface |
US3423644A (en) * | 1967-01-12 | 1969-01-21 | Bissett Berman Corp | Electrolytic cell with housing comprising electrode and seal portions |
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US2791473A (en) * | 1955-01-31 | 1957-05-07 | Gen Electric | Elapsed time indicator |
US3119754A (en) * | 1961-02-10 | 1964-01-28 | Sperry Rand Corp | Elapsed time indicator |
US3210662A (en) * | 1961-07-20 | 1965-10-05 | United Nuclear Corp | Electrolytic indicator with an electrode having a thin frangible coating thereon |
US3423648A (en) * | 1966-01-10 | 1969-01-21 | Bissett Berman Corp | Electrolytic cell with electrically conductive masking surface |
US3423644A (en) * | 1967-01-12 | 1969-01-21 | Bissett Berman Corp | Electrolytic cell with housing comprising electrode and seal portions |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3564347A (en) * | 1969-01-21 | 1971-02-16 | Sprague Electric Co | Electrochemical timer |
US3679945A (en) * | 1969-09-20 | 1972-07-25 | Matsushita Electric Ind Co Ltd | Electric quantity memory element |
US3700974A (en) * | 1971-11-10 | 1972-10-24 | Edward J Plehal | Electrolytic cell with inner electrode having non-reactive surface |
US3949279A (en) * | 1971-11-12 | 1976-04-06 | P. R. Mallory & Co., Inc. | Recessed anode with particulate metal deposit |
US4164066A (en) * | 1971-11-12 | 1979-08-14 | P. R. Mallory & Co., Inc. | Fabrication of anodes by plasma spray deposition |
US3956676A (en) * | 1973-11-02 | 1976-05-11 | P. R. Mallory & Co., Inc. | Electrical device having anode riser assembly with polymeric film means |
US9164493B2 (en) | 2001-12-13 | 2015-10-20 | Vision Works Ip Corporation | Time dependent-temperature independent color changing label |
US9632485B2 (en) | 2002-12-13 | 2017-04-25 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9606512B2 (en) | 2002-12-13 | 2017-03-28 | Vision Works Ip Corporation | Environment dependent—temperature independent color changing label |
US10274900B2 (en) | 2002-12-13 | 2019-04-30 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9188962B2 (en) | 2011-11-01 | 2015-11-17 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9395699B2 (en) | 2011-11-01 | 2016-07-19 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US9298167B2 (en) * | 2011-12-23 | 2016-03-29 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US20130163392A1 (en) * | 2011-12-23 | 2013-06-27 | Vision Works Ip Corporation | Timing system and device and method for making the same |
US10338537B2 (en) | 2014-09-08 | 2019-07-02 | Vision Works Ip Corporation | Indicators for external variables consisting of singular and multiple depletion cells |
US10318604B2 (en) | 2017-02-13 | 2019-06-11 | Vision Works Ip Corporation | Electronically readable system and device with changing codes |
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