High temperature sealing material

Details High temperature sealing material High temperature sealing material

2002-07-10

2004-12-07

Sample, David (Department: 1755)

Compositions: ceramic

Ceramic compositions

Glass compositions, compositions containing glass other than...

C501S017000, C501S018000, C501S032000, C429S006000, C429S006000, C065S036000

Reexamination Certificate

active

06828263

ABSTRACT:

BACKGROUND OF THE INVENTION
The invention concerns a glass composition for use as sealing material in fuel cells! preferably in the solid oxide fuel cells (SOFC) of the stacked planar type. Typically, such fuel cells are composed of Y-stabilized ZrO
2
, (YSZ) electrolyte with electrodes and contact layers to the electron conducting plate Interconnect (IC), which makes the series connection between the cells. Gas tight sealings are vitally important for the performance, durability and safety operation of the fuel cells including the manifold and heat exchanger.
The difficulties in providing a suitable sealing material are numerous:
The sealing material should be able to adhere to the fuel cell components at a heat treatment not higher than 1300° C. which is the maximum temperature heat treatment of a fuel cell stack, and be resilient in order to take up deformations, e.g. due to TEC differences between the fuel cell components, and at the same being able to withstand a certain overpressure at the operation temperature which require a viscosity of more than 10
5
dPas·s. The thermal expansion coefficient (TEC) should be in the range 9-13·10
−6
K
−1
in order not to initiate cracks in the fuel cell components. Furthermore, the sealing material has to be stable over a time span of say 40.000 h without deteriorating crystallization or reactions with the other materials as well as with the ambient gasses, atmosphere containing steam, methane, hydrogen, carbonmonoxide and carbondioxide or nitrogen and oxygen.
Glass or glass ceramic seals may fulfil the requirements established above and according to literature quite a range of potential glasses have been reported:
TABLE 1
SOFC SEALING MATERIALS
Alkaline oxide silicate glasses
Na
2
O—CaO—SiO
2
Li
2
O—ZnO—Al
2
O
3
—SiO
2
and MgO—ZnO—SiO
2
Alkali-Al
2
O
3
—SiO
2
Alkali-B
2
O
3
—SiO
2
Na
2
O—SiO
2
Li
2
O—SiO
2
Mica Glass Ceramics
Commercially available mica glass-ceramic
Alkaline-Earth Oxide Borosilicate/Silicaborate Glasses
Alkaline-Earth-B
2
O
3
—SiO
2
SrO—La
2
O
3
—Al
2
O
3
—B
2
O
3
—SiO
2
/
SiO
2
—B
2
O
3
BaO—As
2
O
3
—Al
2
O
3
—B
2
O
3
—SiO
2
Alkaline-Earth Alumina Silicates
SiO
2
based glass-ceramics
MgO—Al
2
O
3
—SiO
2
CaO—Al
2
O
3
—SiO
2
According to Ley et al. (1996), each of these glass types have a drawback: the alkalis and alkali silicates and borates will react with the fuel cell components. The alkali borate glasses have too low TEC and soda-lime glasses too low viscosity.
In contrast several glass compositions within the SrO—La
2
O
3
—Al
2
O
3
—B
2
O
3
—SiO
2
system should be suitable (K. L. Ley, M. Krumpelt, R. Kumar, J. H. Meiser & I. Bloom, 1996, J. Mater. Res., Vol. 11, No 6, pages 1489-1493).
The present invention is in contrast to the conclusion of the authors above based on highly viscous polymerized alkali-alumina-silicate glass seals, which are reluctant to crystallize at elevated temperature. An example of a highly polymerized glass is pure SiO
2
glass, which has a polymerized 3D network (as the crystalline phase, quartz) based on SiO
4
4−
tetrahedra, where each oxygen ion connects two Si ions (B. E. Warren & Biscoe, 1938, J. Am. Ceram. Soc. 21, page 29). By addition of group I, II and III metal oxides this network is broken and the softening point, the viscosity and the melting point decreases significantly. It is possible to retain a polymerized structure of the melt with a high viscosity by substituting SiO
2
with NaAlO
2
(D. C. Boyd & D. A. Thompson, in Ullmann, Vol. 11, page 815). Accordingly, a NaAlSi
3
O
8
melt has a high viscosity of 10
8.5
dPas·s at 1120° C. (H. Rawson, 1967, Academic Press, London and New York, page 89). This melt is assumed to have a 3D network (Si
1-x
, Al
x
)O
4
4−x−
network structure, where xNa
+
compensate the extra negative charge, similar to the 3D network in the mineral albite with the same composition. Crystallization from such a highly viscous melt held nearly 100° C. below the melting point may take years due to the high viscosity (H. Rawson, 1967). By addition or subtraction of NaAlSiO
4
, SiO
2
, it is possible to reach two eutectic melting temperatures at 1062° and 1068° at compositions: NaAlSiO
4
: SiO
2
, 37.0:63.0 wt % and 65.0:35 wt %, respectively (J. F. Schairer, J. Geol. 58, No 5, 514, 1950). For the system: KAlSiO
2
, SiO
2
, an eutectic point of 990±20° C. may be obtained at a composition of KAlSiO
4
: SiO
2
equal to 32.8:67.2 wt % (J. F. Schairer, N. L. Bowen, Bull Soc, Geol. Finland, 20.74 (1947).
The TEC of a NaAlSi
3
O
8
glass is 7.5·10
−6
K
−1
, which is lower than the SOFC components 10.0-13·10
−6
. The TEC of the albite glass can be increased slightly by addition of NaAlO
2
, whereas a value of 10.4·10
−6
K
−1
may be obtained by addition of Na
2
O giving a cation composition of Na
3.33
Al
1.67
Si
5
(O. V. Mazurin, M. V. Streltsina & T. P. Shvaikoshvaikoskaya, Handbook of glass data, part C, page 371, from K. Hunold & R. Brûckner, 1980a, Glastech. Ber. 53, 6, pages 149-161). Higher values up to more than 12×10
−6
K
−1
can be obtained by further addition of Na
2
O according to these authors.
An example of a NaAlSi
3
O
8
+Na
2
O TEC matched glass for sealing yttria stabilized zirconia is shown in FIG.
1
. Addition of K
2
O will have an even higher effect on the TEC.
Addition of Na
2
O and K
2
O alone will decrease the viscosity and the T
glass
and T
softening
as illustrated in Table 2 for Na
2
O, which will be necessary for operation temperatures below 1000° C.
TABLE 2
T
g
(° C.)
T
s
(° C.)
11.8 Na
2
O − 19.4Al
2
O
3
− 68.7SiO
2
786
910
17.1 Na
2
O − 14.9Al
2
O
3
− 68.0SiO
2
515
607
11.8 Na
2
O − 19.4Al
2
O
3
− 68.7SiO
2
+ YSZ
814
929
Alkali-addition, however, will cause an increased reaction rate with the other fuel cell components and an evaporation of sodium and potassium, so that this solution is best suited for low operation temperatures. Small amounts of BO
3
addition can also be used to decrease the melt temperature and viscosity. An alternative to the addition of alkalies in order to increase the TEC is to use fillers with a high TEC and (Y. Harufuji 1992: Japanese Patent No 480,077 A2) and (Y. Harufuji 1994, Japanese Patent No 623,784 A2) thus Harufuji mentions different fibres of carbon, boron, SiC, polytitanocarbosilane, ZrO
2
and Al
2
O
3
and powders of Al
2
O
3
, ZrO
2
, SiO
2
, MgO, Y
2
O
3
and CaO and Al, Ag, Au and Pt. To this list we can add stabilized ZrO
2
, TiO
2
, MgO—MgAl
2
O
4
composites, (Mg,Ca)SiO
3
, Mg
2
SiO
4
, MgSiO
3
, CaSiO
3
, CaZrO
3
and M
II
AlSi
2
O
8
, where M
II
=Ca, Sr and/or Ba (rare earth oxides, e.g. CeO
2
, Eu
2
O
3
and ThO
2
) (Li
2
Si
2
O
5
may be used at temperatures below 1000° C.).
Other alkalisilicates may be used as fillers for low temperature operation. A combination of alkali and filler addition can be used to obtain optimal TEC, viscosity and the softening point T
s
. Also addition of small amounts (<wt %) B
2
O
3
instead of or together with Na
2
O combined with addition of high TEC fillers mentioned above is a possibility. The filler addition will reduce the exposed surface of the glass and thus the evaporation of the more volatile constituents of the glass.
Deteriorating Reactions May Involve:
(1) SiO evaporation may occur under reducing condition on the anode side condensation may take place in other areas of the fuel cell system. Apparently this process is slow.
(2) Volatile sodium and potassium may react with the other fuel cell materials, e.g. the chromite of the interconnection plate. The evaporation is strongly influenced by the sodium surplus of the glass. For this reason the sealing glasses with alkali/Al-ratios above 1 should only be used in fuel cells with low operation temperatures.
SUMMARY OF THE INVENTION
According to the invention there is provided a glass composition comprising a glass matrix with main components consisting of SiO
2
, Al
2
O
3
and one or more compounds from group I metal oxides, and a filler m

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