GB1586072A - Creación de Inventos y Patentes con Inteligencia Artificial

GB1586072A – Sealing of ceramic electrolyte material in electrochemical cells
– Google Patents

GB1586072A – Sealing of ceramic electrolyte material in electrochemical cells
– Google Patents
Sealing of ceramic electrolyte material in electrochemical cells

Download PDF
Info

Publication number
GB1586072A

GB1586072A
GB18870/77A
GB1887077A
GB1586072A
GB 1586072 A
GB1586072 A
GB 1586072A
GB 18870/77 A
GB18870/77 A
GB 18870/77A
GB 1887077 A
GB1887077 A
GB 1887077A
GB 1586072 A
GB1586072 A
GB 1586072A
Authority
GB
United Kingdom
Prior art keywords
ceramic
metal
annular
elements
shaped
Prior art date
1977-05-05
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

Application number
GB18870/77A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Chloride Silent Power Ltd

Original Assignee
Chloride Silent Power Ltd
Priority date (The priority date 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 date listed.)
1977-05-05
Filing date
1977-05-05
Publication date
1981-03-18

1977-05-05
Application filed by Chloride Silent Power Ltd
filed
Critical
Chloride Silent Power Ltd

1977-05-05
Priority to GB18870/77A
priority
Critical
patent/GB1586072A/en

1977-05-18
Priority to SE7705920A
priority
patent/SE7705920L/en

1977-05-18
Priority to NL7705506A
priority
patent/NL7705506A/en

1977-05-19
Priority to AU25307/77A
priority
patent/AU510297B2/en

1978-05-03
Priority to US05/902,528
priority
patent/US4215466A/en

1978-05-03
Priority to FR7813118A
priority
patent/FR2390024B1/fr

1978-05-04
Priority to JP5285578A
priority
patent/JPS5412416A/en

1978-05-05
Priority to DE19782819815
priority
patent/DE2819815A1/en

1980-03-25
Priority to US06/133,723
priority
patent/US4294897A/en

1981-03-18
Publication of GB1586072A
publication
Critical
patent/GB1586072A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

Classifications

H—ELECTRICITY

H01—ELECTRIC ELEMENTS

H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY

H01M10/00—Secondary cells; Manufacture thereof

H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34

H01M10/39—Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature

H01M10/3909—Sodium-sulfur cells

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B37/00—Joining burned ceramic articles with other burned ceramic articles or other articles by heating

C04B37/02—Joining burned ceramic articles with other burned ceramic articles or other articles by heating with metallic articles

C04B37/023—Joining burned ceramic articles with other burned ceramic articles or other articles by heating with metallic articles characterised by the interlayer used

C04B37/026—Joining burned ceramic articles with other burned ceramic articles or other articles by heating with metallic articles characterised by the interlayer used consisting of metals or metal salts

H—ELECTRICITY

H01—ELECTRIC ELEMENTS

H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY

H01M10/00—Secondary cells; Manufacture thereof

H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34

H01M10/39—Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating

C04B2237/02—Aspects relating to interlayers, e.g. used to join ceramic articles with other articles by heating

C04B2237/12—Metallic interlayers

C04B2237/121—Metallic interlayers based on aluminium

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating

C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates

C04B2237/32—Ceramic

C04B2237/34—Oxidic

C04B2237/343—Alumina or aluminates

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating

C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates

C04B2237/40—Metallic

C04B2237/405—Iron metal group, e.g. Co or Ni

C04B2237/406—Iron, e.g. steel

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating

C04B2237/50—Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating

C04B2237/76—Forming laminates or joined articles comprising at least one member in the form other than a sheet or disc, e.g. two tubes or a tube and a sheet or disc

C04B2237/765—Forming laminates or joined articles comprising at least one member in the form other than a sheet or disc, e.g. two tubes or a tube and a sheet or disc at least one member being a tube

C—CHEMISTRY; METALLURGY

C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES

C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE

C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating

C04B2237/50—Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating

C04B2237/84—Joining of a first substrate with a second substrate at least partially inside the first substrate, where the bonding area is at the inside of the first substrate, e.g. one tube inside another tube

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

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

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION

Y10T29/00—Metal working

Y10T29/49—Method of mechanical manufacture

Y10T29/49002—Electrical device making

Y10T29/49108—Electric battery cell making

Y10T29/4911—Electric battery cell making including sealing

Description

PATENT SPECIFICATION
Application No 18870/77 ( 22) Complete Specification Filed 4 May 1978
Complete Specification Published 18 Mar 1981
INT CL 3 CO 4 B 37/02 HOM 10/39 ( 11) Filed 5 May 1977 ( 52) Index at Acceptance B 3 V HIB ( 72) Inventor:
PETER JOHN BINDIN ( 54) IMPROVEMENTS IN OR RELATING TO THE SEALING OF CERAMIC ELECTROLYTE MATERIAL IN ELECTROCHEMICAL CELLS ( 71) We, CHLORIDE SILENT POWER LIMITED, a British Company, of 52 Grosvenor Gardens, London, SW 1 W OAU, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:-
This invention relates to the sealing of ceramic electrolyte material into electrochemical cells and is concerned more particularly with the sealing-of cells having tubular ceramic electrolyte material.
Sodium sulphur cells are typical examples of cells having a solid ceramic electrolyte Such cells utilising a molten alkali metal have to operate at elevated temperatures where the electrode materials are liquid Seals necessary to seal these electrode materials within the cells have therefore not only to withstand highly reactive materials at these elevated temperatures but are also subjected to temperature cycling As a typical example, a sodium sulphur cell might contain a beta-alumina electrolyte tube closed at one end and having sodium on one face of the tube, preferably the outer face, and the sulphur/polysulphides on the other face The cell has to be sealed to prevent escape or mixing of these materials and a number of proposals have been made for the sealing of such cells.
Compared with most metals, ceramic materials are generally weak, particularly in tensile strength and it is necessary therefore in any seal for such a cell to ensure that the ceramic material is not overstressed.
It is well-known in a sodium sulphur cell to provide a beta-alumina electrolyte tube with an alpha-alumina tubular extension at its open end so that the end portion is not ionically conductive The alpha-aluminia and beta-alumina have similar coefficients of thermal expansion and the alpha-alumina extension can be secured to the beta-alumina with a glass seal.
The present invention is directed to an improved form of sealing for electrochemical cells having tubular electrolyte material providing a simple and convenient form of manufacture.
According to one aspect of the present invention, a method of sealing annular metal members to the open end of a ceramic electrolyte tube for an electrochemical cell comprises the 50 steps of providing a rigid annular element of a ceramic material having a coefficient of expansion substantially the same as that of the electrolyte material, forming’upper and lower shaped surfaces on said annular ceramic element 55 at or near the ends thereof, the shaping being arranged so that the outside diameter decreases in the direction towards the respective end of the ceramic annular element, putting conical metal elements or coatings over the shaped sur 60 faces, such metal elements or coatings being of a relatively soft metal compared with said annular metal members, putting said annular metal members over the respective soft metal covered upper and lower shaped surfaces of the ceramic 65 element, and then forcing the annular metal members axially together to deform the soft metal so that said metal members are secured on the ceramic element, said ceramic annular element being secured to the electrolyte tube 70 either before putting on the metal elements or after forming the assembly with the metal elements.
With this construction, the soft metal is deformed by the axial pressure to seal the 75 metal elements to the annular ceramic element.
The metal elements, in an electrochemical cell may be closure elements for the regions inside and outside the electrolyte tube They would typically be formed of a metal resistant to the 80 electrochemical reactants in the cell or coated with a suitable coating The annular ceramic element would typically be of substantially greater radial thickness than the electrolyte tube 85 The annular metal elements are preferably of a material having a coefficient of thermal expansion greater than that of the ceramic material The assembly comprising the annular element and the metal elements or coatings and 90 the metal members may be heated either before or while forcing the metal members axially into tight engagement with the ceramic material The material is tightly secured by the pressing on of ( 21) ( 23) ( 44) ( 51) O 0 o to ra) 1 586 072 1039 202 1 586072 the metal members The heating can give a further advantage in that the metal members will contract more than the ceramic on cooling.
The shaped surfaces of the ceramic material may be tapered surfaces, for example with straight tapers, but as described later, preferably an annular groove is formed in each surface of the ceramic The annular metal elements have conical surfaces and these may have a straight taper corresponding to the taper on the ceramic surfaces.
The metal members and the ceramic element may both be coated with the aforementioned soft material and, in this case, the securing of the elements together may be effected by pressure without heating, a cold weld being formed between the two coatings of soft material Preferably however the assembly is heated either before or while the pressure is applied; in this case, the soft metal may conveniently be in the form of separate elements put over the shaped ceramic surfaces before the assembly is heated and the pressure is applied.
The ceramic annular element may be secured, for example with glass, to the end of the electrolyte tube either before putting on the metal elements or after forming the assembly with the metal elements.
It will be seen that with the above-described construction, the hoop stress is taken by the annular ceramic element which can be made quite thick in the radial direction and hence capable of withstanding the stresses which might arise.
By the above-described technique, it becomes readily possible, in a simple operation which can be automated, to secure the metal elements onto the rigid ceramic element The metal elements can conveniently both be made of the same material and this facilitates the sealing operation because the similarly shaped surfaces with the same maximum and minimum diameters may be used and it is readily possible to obtain the same thermal conditions for effecting seals to both of the tapered surfaces since these are both external surfaces.
Preferably at least one annular groove is formed on each of said shaped surfaces of the ceramic material The soft metal can deform into such a groove In the region of the groove, the soft metal deforming into the groove relieves interfacial pressure and thus the provision of such a groove enables the development of interfacial pressure to be avoided except where it is needed More generally such a groove or grooves enables a non-linear pressure distribution to be developed across the shaped surface.
The choice of materials to be used will, in general, depend on the materials in the cell In an electrochemical cell having a liquid alkali metal and a liquid cathodic reactant such as for example sulphur/polysulphides, the various materials would have to be chemically inert with respect to the cell materials at the operating temperature of the cell For a sodium sulphur cell, conveniently the ceramic annular element is formed of alpha-alumina The soft metal interlayer may be formed of aluminium alloy.
Very conveniently the aluminium interlayer between the hard metal and the ceramic is 70 extended beyond the seal region, for example to form an internal protective coating protecting the outer hard metal members for contact with the anodic and cathodic reactants in the cell 75 One of the two hard metal annular members may be formed integrally with an outer casing for the cell This member, which may be formed for example of steel, would be secured on the shaped surface at that end of the ceramic ele 80 ment which is joined to the electrolyte tube, the casing extending from the annular portion around the outside of the electrolyte tube which has the anodic and cathodic reactants on opposite faces Preferably in a sodium sulphur 85 cell, the sodium forming the anode is arranged in the region outside the electrolyte tube and the sulphur/polysulphides forming the cathodic reactant is put inside the electrolyte tube.
According to another aspect of this inven 90 tion, in an electrochemical cell having a ceramic electrolyte tube closed at one end and separating anodic and cathodic reactants, an annular element of ceramic material is sealed with glass to the open end of the electrolyte tube, said 95 annular element having shaped external surfaces such that, over these surfaces, the diameter of the element decreases from a maximum diameter intermediate the ends of the element to minimum diameters at or near the respective ends 100 of the element, soft metal being provided over said shaped surfaces and outer metal elements being provided around said shaped surfaces and secured thereto by the soft metal, one of said metal elements forming part of a housing enclo 105 sing the electrolyte tube and the other of the metal elements forming a top closure extending at least partly across the top of said annular ceramic element.
The following is a description of one embodi 110 ment of the invention, reference being made to the accompanying drawing which is part of a diagrammatic axial section illustrating the construction of a sodium sulphur cell.
Referring to the drawing there is shown part 115 of a cylindrical ceramic electrolyte tube 30 which, in this particular embodiment, is formed of beta-alumina and which serves to separate an anodic region from a cathodic region This electrolyte tube 30 is closed at one end (the 120 lower end in the drawing) In this embodiment the anodic region 31 containing liquid sodium is on the outside of the electrolyte tube 30.
Inside this tube is the cathodic region containing, in the known way, a porous matrix of electron 125 ically-conductive material, e g carbon or graphite fibre 32, impregnated with the cathodic reactant which comprises sulphur/polysulphides.
Centrally within the cathodic region is a cathode current collector This current collector corm 130 1 586 072 prises an outer tube 33 of electrically-conductive material which is impermeable to the cathodic reactant and chemically and electrochemically inert to the cathodic reactant, and within the tube 33 is a conductive metal core 34 with a deformable interface material 35 between the core 34 and the tube 33 The cell has an outer steel housing 36 which extends around the outside of the anodic region 31.
The present invention is concerned more particularly with the sealing of the cell at the open end of the electrolyte tube 30 An annular element 40 which is formed of ceramic material having a coefficient of thermal expansion similar to that of the electrolyte tube 30 but which is an electronic insulator and also an ionic insulator is secured to the upper end of the electrolyte tube Conveniently this member is formed of alpha-alumina and is bonded by glass 41 to the end of the electrolyte tube.
The member 40 has a radial thickness substantially greater than that of the electrolyte tube so as to be capable of withstanding substantially higher radial stresses than the electrolyte tube This member 40 is shaped on its external surface to have two tapered regions 43 and 44.
The lower region 43 tapers from a maximum diameter half way up the height of the element to a minimum diameter at the lower extremity The tapered surface 44 extends over the upper half of the element 40 and is tapered in the opposite sense The two tapers are of substantially the same angle and are linear tapers.
Annular grooves 45, 46 are formed around the element 40 in respective tapered surfaces 43, 44 The outer steel housing 36, at its upper end is flared outwardly as shown at 47 to have a shape corresponding to the taper on the surface 43 A top steel closure member 49 has a downwardly-extending flange portion 50 at an angle conforming to the slope of the tapered surface 44 An interlayer 51 of a deformable metal such as aluminium or aluminium alloy is provided between the flared portion 47 of the housing and the surface 43 and a similar interlayer 52 is provided between the sloping flange portion and the tapered surface 44.
Deformation seals are made between the outer housing 36 and the element 40 and between the top closure 49 and the element 40 by loading the closure member 49 in the direction of the axis of the assembly against a reactive load on the housing 36 This loading is effected at an elevated temperature above the normal working temperature of the cell (which might typically be 3500 C); preferably the seal is effected at a temperature of about 6000 C The loading causes the interlayers 51, 52 to be extensively deformed during relative movement between the housing 36 and the closure 49 This extensive deformation breaks up the oxide surface layer on the material of the interlayers and exposes the pure metal surface Deformation can also scrub oxide layers from the inner surfaces of the housing and the top closure member where they extend over the tapered surfaces.
The freshly exposed metal of the interlayers bonds strongly to the metal housing 36 and the top closure member 49 and also to the alphaalumina element 40 so that all three are sealed 70 and bonded together.
The grooves 45, 46 reduce the area of contact of the tapered surface and thus increase the compressive stress on the interlayer and thereby cause increased deformation These 75 grooves provide a region into which material from the deformed interlayers is able to flow.
This reduces the interfacial pressure in the immediate region of the grooves and hence causes, for any given axial loading of the 80 assembly, increased interfacial pressure in other parts remote from the groove It thereby increases the amount of deformation that is able to occur at a given stress level The provision of such a groove or grooves enables a 85 non-linear pressure distribution to be obtained with the maximum stress occurring in chosen areas.
The interlayers 51, 52 of soft deformable metal might be coatings bonded to one or both 90 of the tapered surfaces but, as illustrated in the drawing, are preferably separate elements which conveniently extend beyond the region of the seal to perform further functions The lower interlayer 51 extends down inside the housing 95 36 to form a protective barrier 54 The anodic region 31 between this barrier 54 and the electrolyte tube 30 is formed as a capillary region or contains a sodium electrode capillary feeder means so that the outer surface of the electro 100 lyte tube 30 can be kept wet with liquid sodium from a sodium reservoir Such an interlayer member 51, 54 may conveniently be formed as a deep drawn tube of aluminium or aluminium alloy with a hemispherical closed lower end 105 Suitable small holes or fissures may be formed in this layer at appropriate locations to allow a restricted feed of sodium metal from the sodium reservoir In a cell having a cylindrical casing, the sodium is conveniently stored in a reservoir 110 (not shown) beyond the closed end of the ceramic electrolyte tube 30 In a cell with a square section housing, the sodium may be stored between the outer surface of the electrolyte tube and the inner surface of the outer 115 casing In such a cell, the housing 36 may be of substantially square cross section over the greater part of its length with a short transformation region from the square cross section to a round cross section at the upper end where 120 the housing is formed with a flared portion 47 of conical form which is sealed to the alphaalumina element 40.
The upper interlayer 52 extends across the top of the alpha-alumina element 40 across 125 the top of the cell to the current collector as a protective lining 55 inside the closure member to give protection against corrosion by the cathodic reactants during operation of the cell.
This interlayer 52, 55 is conveniently also used 130 1 586 072 as an interlayer for a deformation seal 56.
between the closure member and the outer tube 33 of the current collector; this current collector is provided with an internal closure 57 through which electrical connection between the current collector and an external terminal is effected.
In the above-described method of effecting the closure, the assembly is heated It is possible to use cold friction welds if aluminium is coated onto the tapered surfaces of the alumina element and the outer metal components A cold weld enables a faster process time to be obtained for the welding operation The required plating of the aluminium onto the alumina and the metal components may conveniently be effected using an ion plating technique to ensure firm bonding of the aluminium coating onto the components The cold welding technique furthermore would enable the cell to be sealed with the sulphur electrode in place.
On the other hand a process in which the load is applied while the assembly is heated and in which the outer metal elements must shrink onto the alpha-alumina element when the assembly cools ensures high interfacial pressure with a smaller loading in the assembly.
In the specification of Application No.
22211/78 (divided out of the present application) and Cognate No 42149/77 (Serial No.

Claims (19)

1586073), there is claimed a method of sealing
an annular metal element or elements to a cylindrical ceramic element, one of the elements to be sealed together having an external cylindrical surface shaped so that the diameter of that surface varies along the axis and the other element having an inside cylindrical surface shaped so that its inside diameter varies along the axis whereby the shaped surfaces can be nested together, the two elements being pressed together in an axial direction with an interlayer of a deformable metal between said shaped surfaces, the pressure and the relative movement being such as to cause deformation of at least part of the interlayer around the whole of the annular region between the elements with the formation of cold pressure bonds giving hermetic seals between the interlayer material and both the inner and outer elements.
In the above-mentioned specification, there is also claimed an assembly comprising a cylindrical ceramic member having shaped inner and outer surfaces at or near one end of the member, these surfaces being such that the outer diameter decreases towards the end of the member and the inner diameter increases towards the end of the member, and inner and outer annular elements of a hard metal having complementary tapered surfaces bonded to the shaped surfaces of the ceramic member with interlayers of a soft metal between the ceramic and each of the inner and outer elements by cold pressure bonding.
WHAT WE CLAIM IS:1 A method of sealing annular metal members to the open end of a ceramic electrolyte tube for an electrochemical cell comprising the steps of providing a rigid annular element of a ceramic material having a coefficient of expan 70 sion substantially the same as that of the electrolyte material, forming upper and lower shaped surfaces on said annular ceramic element at or near the ends thereof, the shaping being arranged so that the outside diameter 75 decreases in the direction towards the respective end of the ceramic annular element, putting conical metal elements or coatings over the shaped surfaces, such metal elements or coatings being of a relatively soft metal compared with 80 said annular metal members, putting said annular metal members over the respective soft metal covered upper and lower shaped surfaces of the ceramic element, and then forcing the annular metal members axially together to 85 deform the soft metal so that said metal members are secured on the ceramic element, said ceramic annular element being secured to the electrolyte tube either before putting on the metal elements or after forming the assembly 90 with the metal elements.

2 A method as claimed in Claim 1 wherein at least one annular groove is provided in each shaped surface of said rigid annular element of ceramic material, into which groove the soft 95 metal deforms as the annular metal members are forced axially together.

3 A method as claimed in either Claim 1 or Claim 2 wherein said rigid annular element is of substantially greater radial thickness than 100 the electrolyte member.

4 A method as claimed in any of the preceding claims wherein the annular metal elements are of a material having a coefficient of thermal expansion greater than that of the ceramic 105 material.

A method as claimed in any of the preceding claims wherein the shaped surfaces of the ceramic material are tapered surfaces.

6 A method as claimed in Claim 5 wherein 110 the annular metal elements have conical surfaces with a taper corresponding to the taper on the ceramic surfaces.

7 A method as claimed in any of the preceding claims wherein the assembly comprising 115 the annular element and the metal elements or coatings and the metal members is heated either before or while forcing the metal members axially into tight engagement with the ceramic material 120

8 A method as claimed in any of Claims 1 to 6 wherein the metal members and the ceramic element are coated with the aforementioned soft material arid wherein the securing of the elements together is effected by pressure of soft 125 material.

9 A method as claimed in any of Claims 1 to 7 and in which the assembly is heated before or while the pressure is applied wherein the soft metal is in the form of separate elements put 130 1 586072 over the shaped ceramic surfaces.

A method as claimed in any of the preceding claims wherein the ceramic annular element is secured with glass to the end of the electrolyte tube.

11 A method as claimed in any of the preceding claims and for sealing a sodium’ sulphur cell, wherein the ceramic annular element is formed of alpha-alumina.

12 A method as claimed in any of the preceding claims wherein the soft metal interlayer is formed of aluminium of aluminium alloy.

13 A method as claimed in Claim 12 wherein the aluminium interlayer between the annular metal members and the ceramic is extended beyond the seal region to form an internal protective coating protecting the outer annular metal members from contact with the anodic and cathodic reactants in the cell.

14 An electrochemical cell having a ceramic electrolyte tube closed at one end and separating anodic and cathodic reactants, wherein an annular element of ceramic material is sealed with glass to the open end of the electrolyte tube, said annular element having shaped external surfaces such that, over these surfaces, the diameter of the element decreases from a maximum diameter intermediate the ends of the element to minimum diameters at or near the respective ends of the element, soft metal being provided over said shaped surfaces and outer metal elements being provided around said shaped surfaces and secured thereto by the soft metal, one of said metal elements forming part of a housing enclosing the electrolyte tube 35 and the other of the metal elements forming a top closure extending at least partly across the top of said annular ceramic element.

An electrochemical cell as claimed in Claim 14 wherein said annular element is of a 40 radial thickness substantially greater than the wall thickness of the electrolyte tube.

16 An electrochemical cell as claimed in either Claim 14 or Claim 15 and having at least one annular groove in each of said shaped sur 45 faces, into which grooves the soft metal is deformed.

17 An electrochemical cell as claimed in any of Claims 14 to 16 wherein the soft metal extends beyond said annular element of ceramic 50 material to form a protective coating for protecting one or both outer metal elements from contact with the anodic and/or cathodic reactant in the cell.

18 A method of sealing a sodium sulphur 55 cell substantially as hereinbefore described with reference to the accompanying drawing.

19 A cell sealed by the method of any of Claims 1 to 13.
A sodium sulphur cell substantially as 60 hereinbefore described with reference to the accompanying drawing.
BOULT, WADE & TENNANT, Chartered Patent Agents, 34 Cursitor Street, London, EC 4 A 1 PQ.
Printed for Her Majesty’s Stationery Office by MULTIPLEX techniques ltd, St Mary Cray, Kent 1981 Published at the Patent Office, 25 Southampton Buildings, London WC 2 l AY, from which copies may be obtained.

GB18870/77A
1976-05-20
1977-05-05
Sealing of ceramic electrolyte material in electrochemical cells

Expired

GB1586072A
(en)

Priority Applications (9)

Application Number
Priority Date
Filing Date
Title

GB18870/77A

GB1586072A
(en)

1977-05-05
1977-05-05
Sealing of ceramic electrolyte material in electrochemical cells

SE7705920A

SE7705920L
(en)

1976-05-20
1977-05-18

WAY TO REPLACE METAL TO CERAMIC JOINTS

NL7705506A

NL7705506A
(en)

1976-05-20
1977-05-18
Packed sealing gland for sodium sulphur cell – couples joint formation between metallic and ceramic surfaces by conical faces and metal rings

AU25307/77A

AU510297B2
(en)

1976-05-20
1977-05-19
Sulphur-sodium cell seal

US05/902,528

US4215466A
(en)

1977-05-05
1978-05-03
Method of sealing ceramic electrolyte material in electrochemical cells

FR7813118A

FR2390024B1
(en)

1977-05-05
1978-05-03

JP5285578A

JPS5412416A
(en)

1977-05-05
1978-05-04
Method of sealing ceramiccelectrolyte tube

DE19782819815

DE2819815A1
(en)

1977-05-05
1978-05-05

METHOD OF SEALING RING-SHAPED METALLIC SEALING ELEMENTS TO THE OPEN END OF A CERAMIC ELECTROLYTE TUBE FOR AN ELECTROCHEMICAL CELL AND ELECTROCHEMICAL CELL WITH A ROLLED ON AN OPEN END OF A CYLINDER

US06/133,723

US4294897A
(en)

1977-05-05
1980-03-25
Sealing of ceramic electrolyte tubes in electrochemical cells

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

GB18870/77A

GB1586072A
(en)

1977-05-05
1977-05-05
Sealing of ceramic electrolyte material in electrochemical cells

Publications (1)

Publication Number
Publication Date

GB1586072A
true

GB1586072A
(en)

1981-03-18

Family
ID=10119841
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB18870/77A
Expired

GB1586072A
(en)

1976-05-20
1977-05-05
Sealing of ceramic electrolyte material in electrochemical cells

Country Status (5)

Country
Link

US
(2)

US4215466A
(en)

JP
(1)

JPS5412416A
(en)

DE
(1)

DE2819815A1
(en)

FR
(1)

FR2390024B1
(en)

GB
(1)

GB1586072A
(en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

JPS5665213U
(en)

1979-10-25
1981-06-01

DE3166814D1
(en)

1980-07-21
1984-11-29
Chloride Silent Power Ltd
Sodium sulphur cells

GB2080607B
(en)

1980-07-21
1983-08-03
Chloride Silent Power Ltd
Sodium-sulphur cells

DE3033438C2
(en)

1980-09-05
1986-08-21
Brown, Boveri & Cie Ag, 6800 Mannheim

Electrochemical storage cell

DE3117619A1
(en)

1981-05-05
1982-11-25
Brown, Boveri & Cie Ag, 6800 Mannheim

«ELECTROCHEMICAL STORAGE CELL»

JPS5917562U
(en)

1982-07-26
1984-02-02
株式会社ユアサコーポレーション

sodium-sulfur battery

JPS5961480U
(en)

1982-10-18
1984-04-21
株式会社ユアサコーポレーション

sodium-sulfur battery

CH658342A5
(en)

1983-01-07
1986-10-31
Sonval S A

GAS-TIGHT PRIMARY BATTERY.

DE3340264A1
(en)

1983-11-08
1985-05-15
Brown, Boveri & Cie Ag, 6800 Mannheim

ELECTROCHEMICAL STORAGE CELL

US4624732A
(en)

1985-03-25
1986-11-25
501 Oliver Rubber Company
Tire envelope sealing apparatus for recapping tires

JPS61286276A
(en)

1985-06-11
1986-12-16
三菱電機株式会社
Manufacture of ceramic part

JPS63130234A
(en)

1986-11-20
1988-06-02
Sannohashi Seisakusho:Kk
Manufacture of grooved bolt

GB8818050D0
(en)

1988-07-28
1988-09-01
Lilliwyte Sa
Joining of ceramic components to metal components

GB8911944D0
(en)

1989-05-24
1989-07-12
Lilliwyte Sa
Electrochemical cell

US5042847A
(en)

1989-07-20
1991-08-27
Ford Motor Company
Metal to ceramic sealed joint

GB9111982D0
(en)

1991-06-04
1991-07-24
Chloride Silent Power Ltd
An alkali metal energy conversion cell

US6203937B1
(en)

1994-06-22
2001-03-20
Medtronic, Inc.
Hermetic closure seal

US5998728A
(en)

1997-05-21
1999-12-07
Advanced Modular Power Systems, Inc.
Ionically insulating seal for alkali metal thermal to electric conversion (AMTEC) cells

US7041413B2
(en)

2000-02-02
2006-05-09
Quallion Llc
Bipolar electronics package

US6607843B2
(en)

2000-02-02
2003-08-19
Quallion Llc
Brazed ceramic seal for batteries with titanium-titanium-6A1-4V cases

US7166388B2
(en)

2000-02-02
2007-01-23
Quallion Llc
Brazed ceramic seal for batteries

WO2001082397A1
(en)

2000-04-26
2001-11-01
Quallion, Llc
Lithium battery suitable for hybrid electric vehicles

US8603659B2
(en)

2008-10-03
2013-12-10
General Electric Company
Sealing glass composition and article

US8043986B2
(en)

2008-11-13
2011-10-25
General Electric Company
Sealing glass composition, method and article

US8962193B2
(en)

2010-12-22
2015-02-24
Samsung Sdi Co., Ltd.
Electrochemical cell with solid electrolyte having alumina edge portion

US9028997B2
(en)

2012-12-28
2015-05-12
General Electric Company
Ceramic collars for active brazing in sodium-based thermal batteries

Family Cites Families (18)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US1363843A
(en)

1919-12-04
1920-12-28
Henry M Crowther
Spark-plug

US2250355A
(en)

1937-06-08
1941-07-22
Bruck Josef
Packing for insulators in sparking plugs

GB540991A
(en)

1939-07-14
1941-11-07
British Thomson Houston Co Ltd
Improvements in ceramic-to-metal seals

US2267416A
(en)

1939-12-18
1941-12-23
Imp Brass Mfg Co
Flared fitting

US2482178A
(en)

1944-02-29
1949-09-20
Western Electric Co
Composite structure for forming a seal with glass

US3036674A
(en)

1960-02-23
1962-05-29
Rca Corp
Compression seal and sealing material therefor

IT1003398B
(en)

1973-03-19
1976-06-10
British Railways Board

SODIUM-SULFUR ELEMENT HAVING ANODIC AND CATHODIC PARTITION SEPA RATI FROM A SOLID ELECTROLYTE WITH SODIUM ION DUCTOR

GB1513681A
(en)

1974-02-15
1978-06-07
Electricity Council
Sodium-sulphur cells

GB1508803A
(en)

1974-07-03
1978-04-26
Secretary Industry Brit
Electric batteries

US3946751A
(en)

1975-02-18
1976-03-30
General Electric Company
Cell casing with a hermetic mechanical seal and a hermetically sealed sodium-sulfur cell

US3959013A
(en)

1975-06-11
1976-05-25
General Electric Company
Cathode cell casing portion, a cell casing, and a hermetically sealed sodium-sulfur cell

GB1545502A
(en)

1975-06-23
1979-05-10
Secretary Industry Brit
Electric cells having a solid electrolyte

GB1506505A
(en)

1975-07-03
1978-04-05
Chloride Silent Power Ltd
Alkali metal-sulphur cells

FR2333358A1
(en)

1975-11-28
1977-06-24
Comp Generale Electricite

SULFUR-SODIUM ELECTROCHEMICAL GENERATOR

GB1502693A
(en)

1976-02-09
1978-03-01
Chloride Silent Power Ltd
Sealing of electro-chemical devices utilising liquid sodium and a solid ceramic electrolyte permeable to sodium ion

GB1574804A
(en)

1976-05-20
1980-09-10
Chloride Silent Power Ltd
Metal-to-ceramic seals

US4071663A
(en)

1977-04-01
1978-01-31
Interpace Corporation
Battery feedthrough penetrator

US4170694A
(en)

1978-12-04
1979-10-09
Ford Aerospace & Communications Corp.
Hermetically sealed alkali metal battery container

1977

1977-05-05
GB
GB18870/77A
patent/GB1586072A/en
not_active
Expired

1978

1978-05-03
US
US05/902,528
patent/US4215466A/en
not_active
Expired – Lifetime

1978-05-03
FR
FR7813118A
patent/FR2390024B1/fr
not_active
Expired

1978-05-04
JP
JP5285578A
patent/JPS5412416A/en
active
Pending

1978-05-05
DE
DE19782819815
patent/DE2819815A1/en
not_active
Withdrawn

1980

1980-03-25
US
US06/133,723
patent/US4294897A/en
not_active
Expired – Lifetime

Also Published As

Publication number
Publication date

US4294897A
(en)

1981-10-13

JPS5412416A
(en)

1979-01-30

US4215466A
(en)

1980-08-05

FR2390024B1
(en)

1983-08-12

FR2390024A1
(en)

1978-12-01

DE2819815A1
(en)

1978-11-16

Información de contacto