CA2053034C - Sodium-sulfur cell and method of joining solid electrolyte tube and insulative ring - Google Patents

Sodium-sulfur cell and method of joining solid electrolyte tube and insulative ring

Info

Publication number
CA2053034C
CA2053034C CA002053034A CA2053034A CA2053034C CA 2053034 C CA2053034 C CA 2053034C CA 002053034 A CA002053034 A CA 002053034A CA 2053034 A CA2053034 A CA 2053034A CA 2053034 C CA2053034 C CA 2053034C
Authority
CA
Canada
Prior art keywords
solid electrolyte
electrolyte tube
glass
joining
insulative ring
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
Application number
CA002053034A
Other languages
French (fr)
Other versions
CA2053034A1 (en
Inventor
Toshiyuki Mima
Michimasa Fujii
Hirohiko Iwasaka
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.)
NGK Insulators Ltd
Original Assignee
NGK Insulators 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.)
Filing date
Publication date
Priority claimed from JP2290266A external-priority patent/JP2693264B2/en
Priority claimed from JP27338391A external-priority patent/JPH07100632B2/en
Application filed by NGK Insulators Ltd filed Critical NGK Insulators Ltd
Publication of CA2053034A1 publication Critical patent/CA2053034A1/en
Application granted granted Critical
Publication of CA2053034C publication Critical patent/CA2053034C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/24Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/02Frit compositions, i.e. in a powdered or comminuted form
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B37/00Joining burned ceramic articles with other burned ceramic articles or other articles by heating
    • C04B37/003Joining burned ceramic articles with other burned ceramic articles or other articles by heating by means of an interlayer consisting of a combination of materials selected from glass, or ceramic material with metals, metal oxides or metal salts
    • C04B37/005Joining burned ceramic articles with other burned ceramic articles or other articles by heating by means of an interlayer consisting of a combination of materials selected from glass, or ceramic material with metals, metal oxides or metal salts consisting of glass or ceramic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/36Accumulators not provided for in groups H01M10/05-H01M10/34
    • H01M10/39Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature
    • H01M10/3909Sodium-sulfur cells
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings; Jackets or wrappings
    • H01M50/183Sealing members
    • H01M50/186Sealing members characterised by the disposition of the sealing members
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings; Jackets or wrappings
    • H01M50/183Sealing members
    • H01M50/19Sealing members characterised by the material
    • H01M50/191Inorganic material
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • C04B2235/6565Cooling rate
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/02Aspects relating to interlayers, e.g. used to join ceramic articles with other articles by heating
    • C04B2237/10Glass interlayers, e.g. frit or flux
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/30Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
    • C04B2237/32Ceramic
    • C04B2237/34Oxidic
    • C04B2237/343Alumina or aluminates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/64Forming laminates or joined articles comprising grooves or cuts
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/70Forming laminates or joined articles comprising layers of a specific, unusual thickness
    • C04B2237/708Forming laminates or joined articles comprising layers of a specific, unusual thickness of one or more of the interlayers
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/76Forming 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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/76Forming 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
    • C04B2237/765Forming 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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/82Two substrates not completely covering each other, e.g. two plates in a staggered position
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making
    • Y10T29/4911Electric battery cell making including sealing

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Electrochemistry (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Structural Engineering (AREA)
  • Secondary Cells (AREA)

Abstract

An excellent stable sodium-sulfur cell having a high mechanical strength and a very long life is provided. The cell eliminates formation of cracks in a joining portion of the solid electrolyte tube and the insulative ring of the cell with the aid of a solder glass filled in a gap between the solid electrolyte tube and the insulative ring, preferably with the aid of a tapered portion formed at at least one of the solid electrolyte tube and the insulative ring, thereby to completely obviate a direct reaction of active substances of the positive electrode and the negative electrode, overheat and destruction of the cell.
The sodium-sulfur cell, comprises a solid electrolyte tube, an insulative ring, a gap of 100-500 µm formed between the solid electrolyte tube and the insulative ring, and a solder glass filled in the gap for joining the insulative ring to the solid-electrolyte tube.

Description

SODIUM-SULFUR CELL AND METHOD OF
JOINING SOLID ELECTROLYT~ TUBE AND INSULATIVE RING
The present invention relates to a sodium-sulfur cell, particularly a sodium sulfur cell having a solid electrolyte tube joined to an insulative ring which electrically insulates a positive electrode chamber from a negative electrode chamber, and a method of joining the solid electrolyte tube and the insulative ring.
A sodium-sulfur cell is a sealed type high temperature secondary cell which is operated at a high temperature of 300-350~C having a sodium ion-conductive solid electrolyte tube made of ~-alumina, ~"-alumina or the like for separating sodium which is an active substance of the negative electrode from sulfur which is an active substance of the positive electrode.
For a better understanding of the present invention, reference is made to the accompanying drawings, in which:
Figure 1 is a schematic cross-sectional view of an embodiment of the present sodium-sulfur cell;
Figure 2a is a schematic cross-sectional view of another embodiment of the present sodium-sulfur cell;
Figure 2b is an enlarged view of the main portion thereof;
Figures 2c and 2d are enlarged views of another embodiment of the main portion of Figure 2a;
Figure 3a is a schematic cross-sectional view of another embodiment of the present sodium-sulfur cell;
Figure 3b is an enlarged view of the main portion thereof;

.~ 2 ~: , , ' ' -:- .,,, . ~ :

Figures 3c and 3d are enlarged views of another embodiment of the main portion of Figure 3b;
Figure 4a is a schematic cross-sectional view of a conventional sodium-sulfur cell;
Figure 4b is an enlarged view of the main portion thereof;
Figure 5 is an enlarged cross-sectional view of another embodiment of the main portion of Figure 2a; and Figure 6 is a cross-sectional view of an apparatus used for preparation of the present sodium-sulfur cell.
Numbering the drawings.
1 ... solid electrolyte tube 2 ... insulative ring 3 ... lid of positive electrode chamber 4 ... lid of negative electrode chamber 5 ... positive electrode chamber 6 ... negative electrode chamber 7 ... cell vessel 8 ... terminal tube 9 ... solder glass 10 ... gap lla, 12a ... tapered portion of solid electrolyte tube llb, 12b ... tapered portion of insulative ring 13 ... fixing jig 14 ... glass ring 15 ... atmosphere-protecting jig 16 ... crack ~ , . . . :... ., . ~ ~
.. ., , : . : . :
: ,~ . .,.. ,.,,. , : .
:, ~
~ . : ~ :. . .
,, . -A structure of a conventional sodium-sulfur cell is shown in the attached Figure 4a, having a solid electrolyte tube 1, a negative electrode chamber 6 filled with sodium arranged at the inside of the solid electrolyte tube 1, a positi~e electrode chamber 5 filled with sulfur arranged at the outside of the solid electrolyte tube 1, and an insulative ring 2 made of a-alumina joined to the upper end of the outer circumferential surface of the solid electrolyte tube 1 by means of a solder glass 9.
Reference numerals 3 and 4 are metallic lids made of aluminum or coated with aluminum which are joined under pressure and heating to the bottom surface and the top surface of the insulative ring 2 for covering the positive electrode chamber and the negative electrode chamber, respectively. Reference numeral 7 is a cell vessel, and 8 is a negative electrode terminal tube.
A joining portion of the solid electrolyte tube 1 and the lnsulative ring 2 of Figure 4a is shown in enlarged view in the attached Figure 4b, wherein reference numeral 9 is a solder glass made of an alumina-borosilicate series glass, etc.
~ lthough the sodium-sulfur cell of the conventional structure of Figures 4a and 4b has the positive electrode chamber 5 and the negative electrode chamber 6 at the outside and the inside, respectively, of the solid electrolyte tube 1, the sodium-sulfur cell may also be formed by arranging the negative electrode chamber 5 and the positive electrode 6 vice versa, namely at the inside and the outside, respectively, of the solid electrolyte tube 1.
As the sodium-sulfur cell is a type of cell which is operated at a high temperature typically at 300-350 C, it .P 4 ,, i , ,:
,, - : , .

undergoes a large thermal change due to start and stop of its operation, and the amount of ions in the sodium which i~ the active substance is increased or decreased by transfer thereof through the solid electrolyte tube 1 due to charge and discharge of the cell, so that the jolnlng portion of the solid electrolyte 1 and the insulating ring 2 is liable to suffer from a thermal stress or a mechanical stress, and cracks and damage are likely to occur at the solder glass 9 or the solid electrolyte ~ube 1.
Particularly, the joining portion of the solid electrolyte tube 1 and the lnsulative ring 2 of the conventional sodium-sulfur cell as shown in Figures ~a and 4b is more liable to ~uffer from a thermal stress or a mechanlcal stress at a ~oining portion of the solder glass 9 and the upper end corner la of the solid electrolyte 1 due to an internal stress of the solder glas~
9 when the $older glass 9 is corroded by metalllc sodlum or sodlum vapor, and a danger of inducing a crack 16 in the solder glass 9 as shown in Figure 4b ls lncreased. Thus, a very dangerous state ls likely to occur in that sodium or a sodium vapor invades from the negative electrode chamber to the positlve electrode chamber 5 2~ through the crack 16 to directly react with sulfur or a sulfide whlch is the active substance of the positive electrode, thereby generating an extraordlnary excesslve heat which further broadens the crack or breakage 16.
Moreover, the solid electrolyte tube having a bottomed tube shape, separatlng the posltive electrode chamber from the ne~ative electrode chamber ls joined at its upper end to the upper end of the posltlve electrode chamber via the insulative rlng made ~ .~, .

: , ~ : . . :, . : : . :
~, .: .

: . :. :; . .. :
.: ~:
,. ~, ;.,. ; .:
,,, :. .

6~881-395 of ~-alumina for electrically insulating the positive electrode from the negative electrode, and the joining portion is exerted by various stresse~ at the time of ascent or de cent o~ the cell temperature, so that a superior mechanical strength is required for the joining portion whlch desirably should not break over a long period of use. However, the joining portion of the conventional cell has not paid attention to such consideration, 80 that it is rather weak in mechanical strength and poor in corrosion resistant property which is prsne to crack thereby incurring a direct reaction of the active substances of the electrodes with each other resulting in troubles due to overheating of the cells.
As a ~older glass 9 at the joining portion for joining the solid electrolyte tube 1 and the insulative ring 2, an alumina borosilicate series glass is usually used. The joining is effected by a method of in~erting the lower portion of the solid electrolyte tube 1 through the in~ulative rlng 2, inserting a glass ring into a gap formed between the solid electrolyte tube 1 and the insulative ring 2, and then heating and melting the glass rlng in an electric furnace. However, joined bodie~ of the solid electrolyte tubes 1 and the insulatlve rlngs 2 have a large fluctuatlon in mechanical strength and are deflclent in reliability.
~ herefore, an objeat of the present lnventlon is to provide a sodium-sulfur cell which obvlate~ the above drawbacks and maintalns a stable state of joining of the solid electrolyte tube and the lnsulatlve rlng and may be used for a long perlod of .

.

:. i . . ~ , . , ~ - ; ~ '., . ' ;

time without a crack formlng at the joining portion.
Another object of the present invention is to reduce any residual stress remaining in the joinlng glass or solder glass so as to prevent formation of a crack in the solder gla~s even when the solder glass is corroded by the active sodium material or its vapor in the negative electrode chamber.
A further object of the present lnvention is to provide a method of joining the solid electrolyte tube and the insulative ring by means of the joining portion having a high mechani~al strength and a small fluctuation in the mechanical ~trength.
In the first aspect, the present invention is a sodium-sulfur cell, comprising a solid electrolyte tube, an insulative ring, a gap o 100-500 ~m formed between the solid electrolyte tube and the insulative ring, and a solder glass filled in the gap for joining the insulative ring to the solid electrolyte tube.
Preferably, a tapered portion is formed on at least one of the solid electrolyte tube and the insulative ring f or providing a glass reservoir at the end portion of the negative electrode chamber facing the solder glass.
"A tapered portion" formed on the ~olid electrolyte tube or the insulative ring for providing a glass reservoir used herein broadly includes both a smooth linear surface and a curved surface.
Preferably, the solder glass is an alumina borosillcate series glass and maintains a concentration of boron B at a depth of 10 ~m from the surface of the alumina borosilicate series glass in the joining portion to at least 90~ of the concentration of ,. . ,~ ,:
: , . : . .

, .. ~ ,.
~: ,. :. :
:.: :

boron B at a depth of 1000 ~m from the surface of the alumina borosilicate series glass in the joining portion.
In the second aspect, the present invention is a method of joining a solid electrolyte tube and an insulative ring by means of an alumina borosilicate series glass, comprising, defining a small space surrounding a joining portion of the solid electrolyte tube and the insulative rlng with the aid of an atmosphere-protecting jig, and ~oining the solid electrolyte tube and the insulative ring in the small space, while preventing evaporation of components of the alumina borosilicate series glass from the surface o~ the glass.
Hereinafter, the present invention will be explained in more detail with reference to examples.
Example~ 1-15 and ComParative Exa~Ple~ 1-10 In Figure 1, a solid electrolyte tube 1 of a bottomed cylinder shape made of ~-alumina separates a positive electrode chamber 5 filled with sulfur from a negative electrode chamber 6 filled with sodium. An insulative ring 2 made of a-alumina is joined to an outer peripheral surface of an upper end of the solid electrolyte tube 1 with a solder glass 9. The insulative ring 2 is joined, under heating and pressure, between a positive electrode lid 3 at an upper end of a h 8 . .
: , - ' 205~3~

cell vessel 7 and a negative electrode lid 4 having a terminal tube 8 of the negative electrode so that the insulative ring 2 ensures electric insulation between the lids 3 and 4. The insulating ring 2 is spaced from the outer peripheral surface of the solid electrolyte tube 1 by a gap 10 of a given distance, and joined to the solid electrolyte tube 1 with an alumina borosilicate based solder glass filled into the gap 10, so that sodium or sodium vapor as a negative electrode active substance may be prevented from directly reacting with sulfur or sulfide as a positive electrode active substance.
In the present invention, it is necessary to set the gap 10 defined between the outer peripheral surface of the upper end of the solid electrolyte tube 1 and the inner peripheral surface of the insulative ring 2 to a distance S of 100-500 ~m. When the solder glass 9 is filled into the gap 10, the solid electrolyte tube 1 and the insulative ring 2 can be uniformly and assuredly joined together. The above distance was determined by thoroughly examining properties of the solder glass.
If the distance S of the gap 10 is smaller than 100 ~m, the solder glass does not sufficiently flow into the gap 10 on joining with the solder glass, so that the filled state of the solder glass on the side of the end portion of the solid electrolyte tube 1 within the 2~
gap 10 becomes non-uniform, and sufficient corrosion ., ~
.~ ~

205~3~

reslstance against sodium vapor cannot be exhibited.
As a result, a danger arises that the solder glass 9 is cracked. On the other hand, if the distance S is greater than 500 ~m, the filled amount of the solder 0~ glass 9 is so much that mechanical strength thereof decreases, and the solder glass cannot withstand various loads occurring on increase and decrease in temperature of the cell, which may destruct the solder glass.
Preferably, the len~th ~ of a straight portion of the gap 10 is set at at least 3 mm to ensure mechanical strength thereof. Furthermore, preferably, the solder glass 9 to be filled into the gap 10 is composed of an aIumina borosilicate series glass, for example, compris-ing four ingredients of 0-B0 wt% of SiO2, 0-30 wt~ of A12O3, 0-80 wt% of B2O3 and 0-30 wt% of Na2O, and has a coefficient of thermal expansion of substantially equal to or slightly smaller than that of the solid electrolyte tube 1 and the insulating ring 2 to reduce the residual stresses and maintain sufficient joining strength. Moreover, preferably, the solder glass is a glass having a sufficient fluidity giving viscosity in a range of 800-1,200 Pa.S in a temperature range of not more than 1,200~C so that the solder glass may not form a reaction phase with ~-alumina during the joining with the glass solder to decrease the joining strength, and 2~
the glass has small influences upon the filling " ~

' ' :

2 ~ 3 ~

properties and joining strength inside the gap 10 in a heating step during the joining under heating and pressure between the insulative ring 2 and the neyative electrode lid 4 or the positive electrode lid 3 in a post treatment.
Concrete examples of the solder glass 9 used in these Examples are shown in the following Table 1.

Table 1 Composition (wt~) CTE Softening Viscosity No.(X10-6/oc) point [103 Pa.S]
SiO2 A1203 B203 Na20 (~C) (~C) A 65.0 10.0 14.0 11.0 6.0 750 1050 B 70.0 5.0 18.0 7.0 6.1 710 980 C 40.0 15.0 30.0 15.0 6.3 700 990 D 30.0 20.0 40.0 10.0 6.0 690 980 E 70.1 8.1 7.7 13.8 7.0 580 F 65.1 7.4 14.0 13.5 6.9 550 -G 60.0 13.1 15.7 11.2 6.7 545 H 64.9 7.4 16.4 11.3 6.85 520 CTE is an abbreviation of coefficient of thermal expansion Next, a glass ring was prepared from a glass having a composition and physical properties of the glasses A-D shown in the above Table 1. Meanwhile, the lower portion of the solid electrolyte tube 1 was inserted into the insulative ring 2, and the glass rinq was set in a space between the solid electrolyte tube 1 ~/

, 2 ~ 3 4 and the insulative ring 2. The glass ring had an inner diameter greater than the outer diameter of an opened portion of the solid electrolyte tube 1 by 200 ~m, and a weight corresponding to a volume of a gap 10 to be defined by the solid electrolyte tube 1 and the glass ring. The glass ring was then heated at a temperature-increasing rate of 150~C/Hr, maintained at a maximum temperature for 1 hour, and then cooled. The thus joined bodies of the solid electrolyte tube 1 and the insulative ring 2 were evaluated on glass-filling property, cantilever bending strength and durability.
Evaluations were made in the following ways:
With respect to the glass-filling property, a joined body in which the glass was filled into the gap 10 in the entire circumferential direction is expressed with a symbol O, one in which the glass was filled into the gap not in the entire circumferential direction but in 50%
or more of the entire circumferential direction is expressed with a symbol O, and one in which the glass was filled into the gap in less than 50% of the entire circumferential direction is expressed with a symbol x, respectively. With respect to the cantilever bending strength, destruction strengths of each twenty joined bodies (n=each 20) were measured for each case when a load was exerted on a tip portion of the solid electro-lyte tube 1 in a direction perpendicular to the axial ' ' : ~
.. ~
.~ . .
~ : . .

64~81-395 direction thereof in ~he state that the insulative ring 2 was grasped or held. The maximum average strength is taken as 100, and symbols ~ ,~ , ~ and x, respectively, denote a joined body in which the average destruction strength was 95% or more, one in which the average destruction strength was 85% or more and less than 95%, one in which the average destruction strength was 70% or more and less than 85%, and one in which the average destruction strength was less than 70%. With respect to the durability, the joined portions were immersed in metallic sodium at 500~C, and an average life until occurrence of cracks due to corrosion of the glass was measured for each five joined bodies (n=each 5) for each case. The maximum average strength is taken as 100, and symbols ~3, o , ~ and x, respectively denotes a joined body in which the average life was 90% or more, one in which the average life was 70% or more and less than 90%, one in which the average life was 50% or more and less than 70%, and one in which the average life was less than 50%. As shown in the following Table 2, it is acknowledged that the joined bodies according to the present invention have splendid properties and shows results of Comparative Examples 1-10.

:: - ' :
. ~ . ' -: ; :: :
. .~, 2~5~3~
Table 2 Example No. (ym)g~olnlng ~oln~L9 filling lever DUlr~a 1 A100 2.01050 0 ~ O
2 A100 3.01050 0 0 ~ 7 3 A150 2.01050 0 0 4 A150 3.01050 0 0 3 A150 4.01050 0 0 0 6 A250 3.01050 0 0 7 A250 4.01050 0 0 Invention 8 A 4004.0 1050 0 0 g A500 5.01050 0 0 B100 3.01000 0 0 O
11 C100 3.0980 12 C250 5.0980 O ~ ~
13 D150 3.01000 0 0 0 14 D250 3.01000 ~ O O
D350 3.01000 0 0 1 A50 1.01050 0 X O
2 A50 3.01050 X X X
3 A50 3.01150 X X X
Compar- 4 A550 5.01050 0 X
ative 5 B50 3.01000 X X X
6 B550 3.01000 0 X
7 C600 3.0950 ~ X
8 C600 5.0980 ~ X
g D50 3.01000 X X X
D50 3.01200 0 X

As apparent from the above description, the cell of this embodiment can prevent formation of cracks in the joining portion of the solid electrolyte tube and the insulative ring for a long period by using the solder glass as described in the above Table 1 of a desired thickness as a joining agent between the solid .:
, ~

2 ~ 3 ~L

electrolyte tube and the insulative ring, so that the cell can prevent a direct reaction of the active substances of the electrodes with each other thereby to securedly prevent overheat troubles and exceedingly Oh prolong the life of the cell.
Examples 16-45 and Comparative Examples 11-14 In the embodiment shown in Figs. 2b, a solid electrolyte body 1 has at the upper end of the outer circumferential surface thereof a tapered portion lla formed by grinding of the tube 1 with a diamond grinding stone, etc., for forming a glass reservoir at the top portion of the solder glass 9 which is attacked most by sodium or sodium vapor of the positive electrode chamber 6. In Figs. 2c and 2d another embodiments are shown of forming the reservoir at the top portion of the solder glass 9, wherein a tapered portion llb is formed at an insulative ring 2, and tapered portions lla and llb are formed at the solid electrolyte tube 1 and the insulative ring 2, respectively, by grinding, for example. Preferably, the tapered portion lla and llb have a height or depth of around 0.5-2 mm, preferably around 1 mm, an inclination angle ~lla and ~llb to the vertical direction of around 5-75~, preferably 15-~5~.
If the inclination angle 911a and 911b are less than 5~, the stresses tend to concentrate on the top portions of the solder glasses 9, 9 at the tapered portions lla and -~} /s~

-.
:. ~

20~a~3~
.

llb. While, if the inclination angles ~lla and ~llb are larger than 75~, the stresses are likely concentrated on the bottom portions of the solder glasses 9, 9 at the tapered portions lla and llb resulting in frequent occurring of cracks of the solder glasses 9l 9.
Concrete shapes of the tapered portion are shown in the following Table 3.

Table 3 Shape ~a (~-alumina) ~b (a-alumina) 1 non-tapered (0~) non-tapered (0~) 9 0 30 .

Another embodiment of the present sodium-sulfur cell is shown in cross-sectlon in Fig. 3a. This tape of cell in this embodiment has a positive electrode chamber 5 at the inside of the solid electrolyte tube 1, a negative electrode chamber 6 at the outside of the solid ,: - ~

:, -20~34 electrolyte tube 1, and a tapered portion 12b formed at an insulative ring 2 by grinding for providing a glass reservoir at the bottom portion of the solder glass 9 which is likely invaded by sodium or sodium vapor.
Fig. 3b shows this main portion of Fig. 3a in enlarged view for clarification.
In Figs. 3c and 3d ~nother embodiments of the main portion of Fig. 3a are shown in enlarged views, wherein a tapered portion 12a is formed at the solid electrolyte 1, and tapered portions 12a and 12b are formed at the solid electrolyte tube 1 and the insula-tive ring 2, respectively. In the embodiments shown in Fig. 3a-3d, preferably, the tapered portions 12a and 12b have a height or depth of around 0.5-1.5 mm, preferably around 1 mm, an inclination angle ~12a and ~12b to the 1~ .
vertical direction of 5-75~, preferably 15-60~. If the inclination angle ~12a and ~12b are less than 5~, the stresses are likely concentrated on the bottom portions of the solder glasses 9, 9 at the tapered portions 12a and 12b. While, if the inclination angle is larger than 75~, the stresses are likely concentrated on the top portions of the solder glasses 9, 9 at the tapered portions 12a and 12b.
Sodium-sulfur cells constructed in these fashions have glass reservoirs formed by providing a 2~
tapered portion at the top portion of the solder glass 9 "- ~ ;
' I , 2~3Q34 facing the negative electrode chamber as shown in Figs. 2a-~d, and at the bottom portion of the solder glass 9 facing the negative electrode chamber as shown in Figs. 3a-3d, so that they have small residual stresses 06 remaining in the solder glass 9 and they receive less concentrated stresses, such as thermal stress and mechanical stress, etc., on the top portion of the solder glass 9 at the joining portion joined to the upper end of the outer circumferential surface of the solid protective tube 1 in the embodiments shown in Figs. 2a-2d, and on the bottom portion of the solder glass 9 at the joining portion joined to the lower end of the outer circumfer-ential surface of the insulative ring 2 in the embodiments shown in Figs. 3a-3d. This is because the tapered portions have more smooth surfaces by grinding work than non-ground portions, which smooth surfaces can prevent formation of cracks in the solder glass 9~
The joining portion of the solid electrolyte tube 1 made of sintered ~-alumina and the insulative ring made of ~-alumina by means of the solder glass is formed by melting and reacting the solder glass 9 at high temperatures, so that components of the solder glass, i.e., SiO2, A12O3, ~2~3 and Na2O in the case of the present invention, form an intermediate product with ~-alumina at the interface thereof. The intermediate product is rich in Na component and considered weak to /~

~ .; ' , " ' ' ' ' ~''' .

2~5~û3~

corrosion by metallic Na at high temperatures.
The surface of the solid electrolyte body made of the sintered ~-alumina has many undulations due to forming thereof and the stresses are likely concentrated at micro areas thereof. The inventors have found out that when ~-alumina and a-alumina respectively not having a tapered portion is actually joined by the solder glass and subjected to a test of resistance to corrosion by metallic Na at high temperatures, a crack is formed from the surface of ~-alumina at the joining intersurface of ~-alumina and the solder glass. This fact means that the joining interface has uneven distribution of composition and is weak in corrosion resistant property and that the surface shape of ~-alumina is participated largely in the crack formation. From the viewpoint, it is considered that an effect of preventing a crack which is formed on the ~-alumina surface and causes final destruction of the joining portion can be obtained by providing a slight tapering treatment on the ~-alumina facing the end portion of the joining portion which is exposed to metal-lic Na or Na vapor of the negative electrode chamber.
~ he stresses generated in the joining portion of ~-alumina and ~-alumina by means of the solder glass depends principally on a difference between coefficients of thermal expansion (CTE) of the materials constituting 2~
the joining portion. From a practical viewpoint, '-~,; \ /~

: , , \

.

2 ~ 4 particularly the residual stress generated in the solder glass at the time of cooling thereof after joining has to be designed to be minimum, among the stresses generated in the joining portion. The residual stress Oh can be decreased by providing a tapered portion at at least one of ~-alumina and ~-alumina. This is because a wettable shape of the solder glass at the end of the joining portion assumes a dull angle so as to avoid concentration of the stresses.

However, if the end of the worked or tapered surface of ~-alumina is embedded in the solder glass, tensile stresses are concentrated on the end portion of the solder glass. The stresses generated in this portion has a tendency of increasing with increase of edge angle or tapered angle of the tapered portion relative to the longitudinal axis of ~-alumina.
Therefore, it is considered that, when the edge angle is large~ if a crack formed at the joining interface of ~-alumina and the solder glass is developed to the edge portion of the tapered portion, the tensile stresses are liberated resulting in destruction of the cell.

,20 . : ~ . :. : . : .
: . .:: ~ . ...
::

:. :, .: ''. ;,' ~ ' ~ '' ; . .
~ :

2 ~
Table 4 Reaction Time with Hiqh Temperature Metallic Na and Crack Occurrence Sample Glass Reaction time (hr~
shape 100 200 400 1000 2000 4000 16 2 B O O O x x x 17 2 C O O ~ x x x 18 3 A O O O ~ x x l9 3 B O O O x x x 4 B O O O ~ x x 21 4 D O O O O ~ x 22 5 A O O o O O O
23 5 C O O O O o O

26 7 B O O O O O ~
27 7 C O O o O O O
28 8 A O O ~ x x x Example 29 8 C O O ~ x x x 9 A O O O ~ x x 31 9 B O O O x x x 32 9 D O O O O x x 33 10 B O O O ~ x x 34 10 D O O O ~ x x 36 ll C O O O O O x 37 11 D O O O O O ~

42 13 B O O o O O O

11 1 A ~ x x x x x Compar- 12 1 B O ~ x x x x Example 13 1 C O ~ x x x x 14 1 D O ~ x x x x g~
~ &/

. .

-- : ,:: . . :.. - . :
., .
. . .. . . . - ~ . . -.

. . , . ~ .
- ; ~

... :: -., .
. ~ . - .
: ..... , .. : , 2 ~ 3 ~
Examples 46-58 and Comparative Example 15-18 Hereinafter, the effects of the present invention are shown.
In these examples, the glasses of Table 1 are used and samples are prepared in the same manner as described in Examples 1-13.
(Evaluation method of corrosion-resistant properties of samples) The thus obtained joined bodies of sample shapes of Nos. 1-14 of Table 4 are sealed together with metallic Na in securedly air-tight metallic vessels at a high temperature of 400~C in vacuo, and left to stand for a determined time. The high temperature of 400~C in the vessels used herein is a severe condition which is higher than operating temperatures of 300-350~C of sodium-sulfur cells, and corresponds to an acceleration test of about 50 times of 330~C, for example.
The resultant sample are annealed to room temperature, and metallic Na thereof are solved in an alcohol and removed from the joining portions, and then the joining portions joined by the joining glasses A-D are inspected at the metallic Na-contacted surfaces on formation of cracks.
Occurrence or non-occurrence of crocks in the joining portions is checked by immersion of the samples in a damage survey fluorescent liquid and irradiating ~'~

- .. . ~ : :~ :
~, 2 ~ 3 ~

the samples with an ultraviolet ray.
The measurements are made on 20 test pieces for each sample and average values thereof are obtained.
Non-cracked samples are further subjected to the corrosion test.
0~
(Results of evaluation test) The results of the valuation test on the samples are shown in the Table 4. In Table 4, crack occurrence of 0% (no test piece cracked) is shown with a symbol ~, 5% (l~ test piece cracked) with a symbol O, lO-30% (2-6 test pieces cracked) with a symbol ~, and 35% or more (7 or more test pieces cracked) with a symbol x.
As apparent from the above evaluation results, the surface of the tapered portion can be made smooth, and cracks in the joining portions joined by the solder glass can be prevented from occurring, by providing a tapered portion at the solid electrolyte tube and/or the insulative ring by grinding work so as to form a glass reservoir in the joining portion of the solid electro-lyte tube and the insulative ring at the contacting20 portion of the solder glass with metallic Na or Na vapor.
Thus, by providing a tapered portion on at least one of the solid electrolyte tube l and the insulative ring 2 at the joining portion thereof by means of the solder glass, cracks in the joining portion can be completely prevented from occurring, leakage of the '~ ~3 '' "' 2~5~3~

active substance Na from the negative electrode chamber can be prevented, and the dangers of the direct reaction of the active substance Na of the negative electrode chamber with the active substance S of the positive electrode chamber can be eliminated as well as the exce5s/~ c~ ~'n ; danger of generation of an extraordinary ~~the cell, so that a highly safe sodium-sulfur cell of an exceedingly long life can be obtained.
As described above, in the joining method of the present invention, at the time of joining the solid electrolyte tube and the ceramic insulative ring the joining is effected by means of the solder glass while covering the joining portion with the aid of the atmo-sphere protecting jig thereby to prevent the evaporation of the solder glass components from the glass surface.
As a result, a difference between the compositions of the solder glass at the surface and the interior thereof is decreased. Particularly, when a concentration of easily vaporizable boron B is attentioned, the concen~

tration of boron at a depth of 10 ~m from the surface of the glass can be maintained to at least 90% of the concentration of boron at a depth of 1000 ym from the surface of the glass. Because the compositions of the glass at the interior and the surface are uniformed in this way, CTE of the joining portion at the surface and 2~
the interior are also uniformed to reduce the residual , .

2 ~ 3 ~

stresses, so that superior joined bodies having joining portion of high mechanical strength can be obtained.
The difference of the concentration of boron between the interior and the surface of the joining portion or the solder glass is defined as less than 10% as descr.ibed above, because if the difference exceeds 10~, the joining portion and hence the sodium-sulfur cell gradually reach to the levels of conventioned ones.
In this embodiment, a solid electrolyte tube l made of ~-alumina of a shape of one end sealed cylinder having an outer diameter of 30.0 mm and a length of 300 mm, and an insulative ring 2 made of ~-alumina having an outer diameter of 42.0 mm and a height of lO.0 mm, are prepared and set on a fixing jig 13, and a glass ring 14 made of an alumina borosilicate series glass is disposed therebetween, as shown in Fig. 6. The insulative ring 2 has a preliminarily formed tapered portion for determin-ing a height of the glass ring 14. The glass ring 14 has a thickness of 1 mm and a height of 2 mm and a composi-tion of either one of 4 types E-H of compositions as ao shown in the above Table 1, and is a well defoamed one.
A cylinder made of ~-alumina having an outer diameter slightly larger than the solid electrolyte tube l and a shape of covering the glass ring 14 is prepared as an atmosphere-protecting jig 15 and placed on the upper surface of the insulative ring 2. In order to ascertain : : ,.
-2~5i~0~

the effect of the present invention, 5 types of a-e of atmosphere-protecting jig having an inner diameter and a height as shown in the following Table 5 are prepared.
For comparison, joinings are effected without using the atmosphere-protecting jig 15.

Table 6 Shape of Atmosphere-protecting Jig Type Inner diameter (mm) Height (mm)Space volume (cm3) a 30.2 5 5.1 b 30.2 100 102.1 c 30.2 300 306.3 d 31.0 5 5.1 e 32.0 5 5.1 Joining tests are performed in combinations of the glass compositions E-H and the atmosphere-protecting jigs a-e and in a same glass melting condition as those of Examples 1-15. The joinings are effected under condi-tions corresponding to high temperature viscosities of respective glass. For example, in the case of glass E, temperature is raised from room temperature up to a maximum temperature of 1 r 150~C at a temperature-increasing rate of 200~C/hr, held thereat for 1 Hr, decreased to around a glass transition temperature at a temperature-decreasing rate of 200~C/hr, and annealed to room temperature at a temperature-decreasing rate of 20~C/hr.
The thus obtained glass-joining bodies are ,~

:
. . :. .
:: ;

205~34 measured on mechanical strength.
The measuring method is comprised of grasping the upper and the lower surfaces of the insulative ring 2 of the glass-joining body, exerting a moment load on the joining portion by loading a weight or pressure on the sealed end portion of the solid electrolyte 1, and measuring the load at the destruction of the joining portion.
The measurements of destruction of the joining portion are ~ffected on 20 test pieces for each joining condition as described in the following Table 6, and an average load at the destruction and standard deviation thereof are also shown in Table 6. A11 the positions of destruction were at the solder glass joining the solid electrolyte 1 and the insulative ring 2.

~0 ' .t. -~

: .

- 20~3034 Table 6 Load at Glass Shape Destruction (N) Example Average Deviation 46 E a 265 18 47 " b 254 24 -.
48 F a 368 24 49 " b 350 18 " c 330 55 51 " d 325 23 Invention 52 " e 305 65 53 G b 389 16 54 " c 365 55 " e 374 60 56 H a 366 16 57 " c 348 43 58 " d 352 21 E none 133 45 16 F " 186 52 Comparative 17 G .. 200 64 18 H " 154 54 In any composition of the glass, the glass-joining bodies obtained by using the atmosphere-protecting jig 15 have large loads at destruction, exhibiting the remarkable effect of the present invention. In the embodiments using the atmosphere-protecting jig 15, when the protected space volume is small or when the gap between the solid electrolyte tube 1 and the atmosphere-protecting jig 15 is small, the standard deviation which represents scattering of the loads at destruction is small, so that such cases are considered as more splendid combinations from th * - ~

2~a~3~

viewpoint of reliability.
The joining glass portions after destruction were studied on distribution of composition at cross-sections of the joining portions for evaluating the h uniformity or homogeneity of the glass portions.
For that purpose, the glass joining portions are severed along the axial direction of the solid electrolyte tube 1, and the severed surfaces are optically polished, and states of deviation of chemical composition at the surface and the interior of the glass protected by the jig 15 were analyzed using EPMA. The analyses are effected by spot analysis at interior of around 30 ~m and 1000 ~m from the surface of the glass protected by the jig 15. The results are shown in the following Table 7. The analyses are effected also by linear analyses to study distribution of concentrations of specific elements from the surface towards the interior of the glass. The results are shown in the following Table 8.

2~ :

: .:. ~ ;, ~ .. :

, :
. . . -:

2 ~ 3 ~

Table 7 Chemical Composition (wt~) Glass Jig Near the Surface Interior Example Type Shape Sio2 A1203 s203 Na20 SiO2 A1203 8203 Na20 48 F a 65.2 7.4 14.0 13.4 65.1 7.4 14.0 13.5 49 F b 65.3 7.4 13.9 13.4 65.1 7.5 14.0 13.4 tion 50 F c 65.4 7.4 13.8 13.4 65.2 7.5 13.9 13.4 51 F d 65.2 7.5 13.9 13.4 65.1 7.5 14.0 13.4 52 F e 65.4 7.5 13.7 13.4 65.2 7.4 14.0 13.4 Compar- 16 F none 68.5 7.8 9.5 14.2 65.2 7.4 14.0 13.4 ative 17 G none 62.7 13.7 11.5 11.7 60.1 13.1 15.6 11.2 Table 8 Dpeth from the Glass Surface(ym) and Example GTlaSs ShJai~ Element Concentration of Element 48 F a B100 100 100 100 100 100 100 " " Si100 100 100 100 100 100 100 " " Al100 100 100 100 100 100 100 " " Na100 100 100 100 100 100 100 49 F b B100 100 100 100 100 100 100 " " Si100 100 100 100 100 100'100 " " Al100 100 100 100 100 100 100 " " Na100 100 100 100 100 100 100 52 F e B95 95 100 100 100 100 100 " " Si100 100 100 100 100 100 100 " " Al100 100 100 100 100 100 100 " " Na100 100 100 100 100 100 100 16 Fnone B60 65 65 80 100 100 100 " " Si105 105 105 105 100 100 100 " " Al105 105 105 100 100 100 100 " " Na105 105 105 105 100 100 100 17 Gnone B70 75 80 90 100 100 100 " " Si105 105 105 100 100 100 100 " " Al105 105 105 105 100 100 100 " " Na105 105 105 100 100 100 100 ffl_ ~-~ ' 3~

- ~ :

:
J

' 20~3~

As apparent from the above explanations, when the joining of the solid electrolyte tube and the insulative ring by means of a solder glass is effected by the method of defining a small space surrounding the 0~ joining portion of the solid electrolyte tube and the insulative ring with the aid of the atmosphere-protecting jig, and joining the solid electrolyte tube and the insulative ring in the small space, while preventing evaporation of the solder glass components from the surface of the solder glass, a difference of compositions between the surface and the interior of the solder glass can be made small, so that the solder glass becomes uniform. Particularly, in conventional methods of not using an atmosphere-protecting jig, a concentra-tion of boron B at a depth of 10 ~m from the surface of a solder glass in the joining portion is decreased to a very low value of not more than 60~ relative to a concentration of B at a depth of 1000 ~m from the surface of the solder glass. In contrast, in the method of the present invention, the concentration of boron B
at the depth of 10 ym from the solder glass surface is maintained at a very high value of 90~ or more, so that the mechanical strength of the joining portion can be made exceedingly high as compared to that of conventional joining portion.
As described in detail in the foregoing .

-"~ ': , " , ' - - .
.

: . , ::: :
;:
' , 2~5,303~

explanations, the present invention provides a sodium-sulfur cell and a method of joining the solid electrolyte tube and the insulative ring which obviates prior problems, so that it is eminently useful to the development of the industry.
Although the present invention has been explained with specific examples and numeral values, it is of course apparent to those skilled in the art that various changes and modifications thereof are possible without departing from the broad spirit and aspect of the present invention as defined in the appended claims.

Ih ~,' ~i ~ ?

. . .
-,

Claims (8)

1. A method of joining a solid electrolyte tube and an insulative ring by means of an alumina borosilicate series glass, comprising the steps of:
defining a small space surrounding a joining portion between the solid electrolyte tube and the insulative ring with the aid of an atmosphere-protecting jig; and joining the solid electrolyte tube and the insulative ring in the small space;
whereby the atmosphere-protecting jig prevents evaporation of components of the alumina borosilicate series glass from the surface of the glass.
2. A sodium-sulfur cell, comprising a solid electrolyte tube, an insulative ring, a gap of 100-500 µm formed between the solid electrolyte tube and the insulative ring, and a solder glass filled in the gap for joining the insulative ring to the solid electrolyte tube, wherein a tapered portion is formed on at least one of the solid electrolyte tube and the insulative ring for providing a glass reservoir at an end portion of the solder glass which faces the negative electrode chamber.
3. A sodium-sulfur cell, comprising a solid electrolyte tube, an insulative ring, a gap of 100-500 µm formed between the solid electrolyte tube and the insulative ring, and a solder glass filled in the gap for joining the insulative ring to the solid electrolyte tube, wherein the solder glass is an alumina borosilicate series glass and maintains a concentration of boron B at a depth of 10 µm from the surface of the alumina borosilicate series glass in the joining portion between the solid electrolyte tube and the insulative ring to at least 90% of the concentration of boron B at a depth of 1000 µm from the surface of the alumina borosilicate series glass in the joining portion.
4. The sodium-sulfur cell of claim 2, wherein said gap has an axial length of at least 3 mm.
5. The sodium-sulfur cell of claim 2, wherein said solder glass has a viscosity of 800-1200 Pa.S in a temperature range of not more than 1200°C.
6. The sodium-sulfur cell of claim 2, wherein said tapered portion has an inclination angle, with respect to the longitudinal axis of the solid electrolyte tube, of 5°-75°.
7. The sodium-sulfur cell of claim 2, wherein said tapered portion has an inclination angle, with respect to the longitudinal axis of the solid electrolyte tube, of 15°-60°.
8. The sodium-sulfur cell of claim 2, wherein said tapered portion has an inclination angle, with respect to the longitudinal axis of the solid electrolyte tube, of 15°-45°.
CA002053034A 1990-10-25 1991-10-08 Sodium-sulfur cell and method of joining solid electrolyte tube and insulative ring Expired - Fee Related CA2053034C (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2290266A JP2693264B2 (en) 1990-10-25 1990-10-25 Sodium-sulfur battery
JP2-290,266 1990-10-25
JP3-273,383 1991-09-24
JP27338391A JPH07100632B2 (en) 1991-09-24 1991-09-24 Glass bonded body of β-alumina tube and ceramics and bonding method thereof

Publications (2)

Publication Number Publication Date
CA2053034A1 CA2053034A1 (en) 1992-04-26
CA2053034C true CA2053034C (en) 1997-12-02

Family

ID=26550642

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002053034A Expired - Fee Related CA2053034C (en) 1990-10-25 1991-10-08 Sodium-sulfur cell and method of joining solid electrolyte tube and insulative ring

Country Status (4)

Country Link
US (1) US5196277A (en)
EP (2) EP0482785B1 (en)
CA (1) CA2053034C (en)
DE (2) DE69131538T2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4309069A1 (en) * 1993-03-20 1994-09-22 Licentia Gmbh Method of connecting the end faces of two ceramic parts in a vacuum-tight manner
DE4336236C1 (en) * 1993-10-23 1995-01-05 Abb Patent Gmbh Electrochemical storage cell
DE19859563B4 (en) * 1998-12-22 2008-01-24 Basf Ag Improved process for the electrochemical production of alkali metal from alkali metal amalgam
EP1431422B1 (en) * 2002-12-16 2006-12-13 Basf Aktiengesellschaft Method for manufacturing lithium
GB2421238A (en) 2004-12-16 2006-06-21 Basf Ag Solid polycrystalline potassium ion conductor having beta-alumina structure
US8603659B2 (en) * 2008-10-03 2013-12-10 General Electric Company Sealing glass composition and article
FR2947540B1 (en) 2009-07-03 2012-01-06 Commissariat Energie Atomique GLASS COMPOSITIONS FOR JOINTS OF APPLIANCES OPERATING AT HIGH TEMPERATURES AND ASSEMBLY METHOD USING THEM.
US8757471B2 (en) * 2012-08-27 2014-06-24 General Electric Company Active braze techniques on beta-alumina
CN103123221B (en) * 2012-12-12 2015-08-05 上海电气钠硫储能技术有限公司 A kind of device for sodium-sulphur battery earthenware sintering
CN103500856B (en) * 2013-10-17 2015-10-28 上海电气钠硫储能技术有限公司 A kind of sodium-sulphur battery
DE102013224111B4 (en) * 2013-11-26 2017-01-12 Schott Ag Sodium-resistant joining glass and its use, joint connection, energy storage device and / or energy generating device
US20170043424A1 (en) * 2015-08-10 2017-02-16 General Electric Company Process for joining metallic and ceramic structures

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
JPS5827565B2 (en) * 1977-09-19 1983-06-10 松下電器産業株式会社 Magnetic head and its manufacturing method
GB2029817A (en) * 1978-09-06 1980-03-26 Thorn Electrical Ind Ltd Sealing of ceramic and cermet partds
DE3412206A1 (en) * 1984-04-02 1985-10-10 Brown, Boveri & Cie Ag, 6800 Mannheim ELECTROCHEMICAL STORAGE CELL
US4661424A (en) * 1985-10-04 1987-04-28 Yuasa Battery Co. Sodium-sulfur storage battery
DE3615240A1 (en) * 1986-05-06 1987-11-12 Bbc Brown Boveri & Cie ELECTROCHEMICAL STORAGE CELL
US4792348A (en) * 1987-03-02 1988-12-20 Powerplex Technologies, Inc. Method of forming glass bonded joint of beta-alumina
GB2207545A (en) * 1987-07-28 1989-02-01 Lilliwyte Sa Glass seal for sodium-sulphur cells
DE3736843A1 (en) * 1987-10-30 1989-05-11 Asea Brown Boveri METHOD FOR JOINING METAL AND CERAMIC MATERIALS
JPH02236970A (en) * 1989-03-10 1990-09-19 Ngk Insulators Ltd Bonding glass beads for forming sodium-sulfur battery and bonding method using the same

Also Published As

Publication number Publication date
EP0632515B1 (en) 1999-08-18
EP0482785A2 (en) 1992-04-29
EP0632515A2 (en) 1995-01-04
DE69112335T2 (en) 1996-04-25
DE69131538T2 (en) 2000-01-20
CA2053034A1 (en) 1992-04-26
US5196277A (en) 1993-03-23
EP0482785A3 (en) 1993-08-25
DE69131538D1 (en) 1999-09-23
EP0482785B1 (en) 1995-08-23
DE69112335D1 (en) 1995-09-28
EP0632515A3 (en) 1996-06-26

Similar Documents

Publication Publication Date Title
CA2053034C (en) Sodium-sulfur cell and method of joining solid electrolyte tube and insulative ring
EP0660810B1 (en) Sealing members for alumina arc tubes and method of making the same
EP2327118B1 (en) Seal ring and associated method
CA2042771C (en) Glass joint body and method of manufacturing the same
KR102398188B1 (en) Method for joining ceramic to metal, and sealing structure thereof
CN113871804B (en) Base body for a feed-through conductor and housing part of a housing, in particular of a battery housing having such a base body
US4215466A (en) Method of sealing ceramic electrolyte material in electrochemical cells
US3985576A (en) Seal for energy conversion devices
US4413043A (en) Electrochemical storage cell
KR102709875B1 (en) Joint, electrical feedthrough, and sensor
JPH11111225A (en) Closure for discharge lamp
JP3479187B2 (en) Solid electrolyte tube and method for producing the same
JP2619061B2 (en) Bonding glass for forming sodium-sulfur battery and method for bonding bottomed cylindrical solid electrolyte and insulator ring using the bonding glass
JP3205851B2 (en) Sodium-sulfur battery and manufacturing method thereof
JP3292994B2 (en) Sodium-sulfur battery
JPH11307118A (en) Glass joined body of solid electrolyte body and insulating member, method for producing the same, and high-temperature secondary battery using this glass joined body
JP2693264B2 (en) Sodium-sulfur battery
GB2140608A (en) Energy conversion devices using liquid sodium and beta alumina ceramic electrolyte material
JPH03291860A (en) Sodium sulpher cell
JPH0585844A (en) Glass joining body of beta-alumina tube and ceramic and its joining method
JPH04175271A (en) Glass joining body and production thereof

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed