Background of the Invention
1. Field of the Invention
[0001] The present invention relates to zirconium-based alloys suitable for use in nuclear
reactor service, and more specifically for use in the cladding of fuel elements.
2. Description of Related Art
[0002] Zirconium-based alloys have long been used in the cladding of fuel elements in nuclear
reactors. A desirable combination is found in zirconium by virtue of its low thermal
neutron cross-section and its generally acceptable level of resistance to corrosion
in a boiling water reactor environment. Zircaloy 2, a Zr-Sn-Ni-Fe-Cr alloy, has enjoyed
widespread use and continues to be used at present in nuclear reactor applications.
This alloy has provided adequate performance in reactor service, but also possesses
some deficiencies which have prompted further research to find materials which would
provide improved performance. Zircaloy 4 was one alloy developed as a result of that
research. This alloy essentially eliminates the Ni (0.007% max. wt. percent) from
a Zircaloy 2-type alloy. Zircaloy 4 was developed as an improvement to Zircaloy 2
to reduce problems with hydriding, which causes Zircaloy 2 to become brittle when
cooled to ambient temperatures (e.g. when the reactor is shut down) after absorbing
hydrogen at higher temperatures.
[0003] The Zircaloy alloys are among the best corrosion resistant materials when tested
in water at reactor operating temperatures (approx. 290°C) in the absence of the
radiation from the nuclear fission reaction. The corrosion rate under those conditions
is very low and the corrosion product is a uniform, tightly adherent, black ZrO₂ film/layer.
In actual service, however, the Zircaloy is irradiated and is also exposed to radiolysis
products present in reactor water. The corrosion resistance properties of Zircaloy
deteriorate under these conditions and the corrosion rate thereof is accelerated.
[0004] Research efforts directed at improving the corrosion properties of the zirconium-based
alloys have yielded some advances. Corrosion resistance has been enhanced in some
instances through carefully controlled heat treatments of the alloys either prior
to or subsequent to material fabrication. Added heat treatment cycles, however, generally
increase the expense of making finished products, and in those instances where an
installation requires welding to be performed, the area affected by the heat of the
welding operation may not possess the same corrosion resistance characteristics as
the remainder of the article. Variations in the alloying elements employed and the
percentages of the alloying elements have also been propounded in an effort to address
corrosion-resistance deterioration of these alloys.
[0005] The deterioration under actual reactor conditions of the corrosion resistance properties
of Zircaloy is not manifested in merely an increased uniform rate of corrosion. Rather,
in addition to the black ZrO₂ layer formed, a localized, or nodular corrosion phenomenon
has been observed especially in boiling water reactors (BWR). In addition to producing
an accelerated rate of corrosion, the corrosion product of the nodular corrosion reaction
is a highly undesirable white ZrO₂ bloom which is less adherent and lower in density
than the black ZrO₂ layer.
[0006] The increase rate of corrosion caused by the nodular corrosion reaction will be
likely to shorten the service life of the tube cladding, and also this nodular corrosion
will have a detrimental effect on the efficient operation of the reactor. The white
ZrO₂, being less adherent, may be prone to spalling or flaking away from the tube
into the reactor water. On the other hand, if the nodular corrosion product does not
spall away, a decrease in heat transfer efficiency through the tube into the water
is created when the nodular corrosion proliferates and the less dense white ZrO₂ covers
all or a large portion of a tube.
[0007] Actual reactor conditions cannot be readily duplicated for normal laboratory research
due to the impracticality of employing a radiation source to simulate the irradiation
experience in a reactor. Additionally, gaining data from actual use in reactor service
is an extremely time consuming process. For this reason, there is no conclusory evidence
in the prior art which explains the exact corrosion mechanism which produces the nodular
corrosion. This limits, to some degree, the capability to ascertain whether other
alloys will be susceptible to nodular corrosion before actually placing samples made
from these alloys into reactors.
[0008] Laboratory tests conducted under the conditions normally experienced in a reactor
(absent radiation) at approximately 300°C and 1000 psig in water, will not produce
a nodular corrosion product on Zircaloy alloys like that found on Zircaloy alloys
which have been used in reactor service. However, if steam is used, with the temperature
increased to over 500°C and the pressure raised to 1500 psig, a nodular corrosion
product like that found on Zircaloy in reactor service can be produced on Zircaloy
alloys in laboratory tests. Specimens of Zircaloy alloys which are annealed at 750°C
for 48 hours are particularly susceptible to nodular corrosion under these test conditions.
These annealed Zircaloy specimens will produce, in tests run for relatively short
times, i.e. 24 hours, a degree of nodular corrosion comparable to that of Zircaloy
tube cladding in actual reactor service. At this higher temperature and pressure,
a simulated nuclear reactor environment is provided which will allow researchers
to determine the susceptibility of new alloys to nodular corrosion. Results of these
tests can be generally compared to those of Zircaloy specimens tested under the same
conditions.
[0009] Any new alloy which would be considered as a suitable alternate or replacement for
the Zircaloy alloys must not only be less susceptible than the Zircaloy alloys to
nodular corrosion, but should maintain acceptable uniform corrosion rates, to ensure
sufficient service life.
[0010] It is therefore a principal object of the present invention to provide a group of
alloys having improved corrosion resistance characteristics in a nuclear reactor
environment.
[0011] It is another important object of the present invention to provide a group of alloys
which do not depend on carefully controlled heat treatment for their corrosion resistance
properties.
Summary of the Invention
[0012] The present invention relates to zirconium-based alloys which, in one preferred embodiment,
consist essentially of about 0.5 to 2.5 weight percent bismuth, approximately 0.5-1.0
weight percent of a solute composed of a member selected from the group consisting
of molybdenum, niobium, tellurium and mixtures thereof, and the balance being zirconium.
[0013] In another preferred embodiment, the corrosion resistant alloys consist essentially
of about 0.5 to 2.5 weight percent of bismuth, 0.3-1.0 weight percent of a solute
composed of tellurium, and the balance zirconium.
[0014] In another preferred embodiment the amount of bismuth is in the range of about 0.7-2.0%
by weight of the alloy.
[0015] In another preferred embodiment, the corrosion-resistant alloys consist essentially
of about 0.5 to 2.5 weight percent of a mixture of tin and bismuth, approximately
0.5-1.0 weight percent of a solute composed of a member selected from the group consisting
of molybdenum, niobium, tellurium and mixtures thereof, and the balance being zirconium.
[0016] In another preferred embodiment, the alloys consist essentially of about 0.5-2.5
weight percent of a mix ture of tin and bismuth, a solute composed of tellurium and
the balance zirconium.
[0017] In another preferred embodiment, the amount of the tin-bismuth mixture is in the
range of 2.0-2.2 percent by weight.
[0018] In other preferred embodiments, the alloy will further consist essentially of 0.09
to 0.16 weight percent of oxygen.
[0019] In another preferred embodiment the alloy consists essentially of about 0.7-2.0 weight
percent bismuth, a solute composed of niobium and molybdenum, the amount of niobium
being substantially 0.5% by weight, the amount of molybdenum being substantially 0.5%
by weight, and the balance zirconium.
[0020] In another preferred embodiment, the alloy consists essentially of about 0.7-2.0
weight percent bismuth, a solute composed of niobium and molybdenum, the amount of
niobium being substantially 0.3 weight percent, the amount of molybdenum being substantially
0.3 weight percent, and the balance zirconium.
[0021] In another preferred embodiment, the alloy consists essentially of about 0.7-2.0
weight percent bismuth, a solute composed of niobium and tellurium, the amount of
niobium being substantially 0.3 weight percent, the amount of tellurium being substantially
0.3 weight percent, and the balance zirconium.
[0022] In another preferred embodiment, the alloy consists essentially of about 0.7-2.0
weight percent bismuth, a solute composed of molybdenum, tellurium and niobium, the
amount of each being substantially 0.2 weight percent, and the balance zirconium.
[0023] In another preferred embodiment, the alloy consists essentially of about 2.0-2.2
weight percent of a mixture of tin and bismuth, a solute composed of niobium and
molybdenum, the amount of niobium being substantially 0.3 weight percent, the amount
of molybdenum being substantially 0.3 weight percent, and the balance zirconium.
[0024] In another preferred embodiment, the alloy consists essentially of about 2.0-2.2
weight percent of a mixture of tin and bismuth, a solute composed of niobium and
tellurium, the amount of niobium being substantially 0.3 weight percent, the amount
of tellurium being substantially 0.3 weight percent, and the balance zirconium.
[0025] In another preferred embodiment, the alloy consists essentially of about 2.0-2.2
weight percent of a mixture of tin and bismuth, a solute composed of molybdenum,
tellurium and niobium, the amount of each being substantially 0.3 weight percent,
and the balance zirconium.
[0026] These alloys provide increased resistance to nodular corrosion in high pressure and
temperature steam testing, and will maintain acceptable uniform corrosion rates in
water and steam tests.
Detailed Description of the Invention
[0027] The alloys of the present invention will provide sufficient resistance to uniform
corrosion to be considered for nuclear reactor service. The alloys of the present
invention have demonstrated improved resistance to nodular corrosion.
[0028] There are several parameters which should be considered in choosing alloying elements
for the candidate Zr-based alloys to be used for fuel cladding in boiling water reactor
service. The thermal neutron cross-section of the element is preferably relatively
low to permit products of the fission reaction to easily pass through the fuel rods
thereby allowing the boiling water reactor operate efficiently. The cost of the material
should be taken into account, and must not be prohibitively high. The ease or difficulty
with which an alloy containing the element or elements and zirconium can be produced
must also be considered. It is further desired that the element or elements will
enhance the corrosion resistance properties of the zirconium under actual or simulated
boiling water reactor conditions.
[0029] The thermal neutron cross-section of an element is generally a known property of
the element if it has ever come under consideration for use in a nuclear reactor.
The costs of the materials can be ascertained from historic price data, with extrapolation
if required. The alloying process of the alloys of the present invention is similar
to conventional methods for alloying zirconium and thus ease of alloying is fairly
predictable. The alloying is accomplished preferably by arc melting a zirconium billet
having a suitable amount of the alloying metals encased in a hollow portion of the
billet. This molten metal is then cast as an alloy billet, which will then be subject
to finishing processes to produce final shapes.
[0030] Generally, the most difficult of these parameters to predict is whether the element
will contribute to the enhancement of corrosion resistance.
[0031] The addition of tin to zirconium has been practiced in the art prior to this invention,
as evidenced by Zircaloy alloys and other known zirconium-based alloy compositions.
The presence of Sn, which stabilizes the α-form of Zr, primarily contributes to the
strength of the alloy, although there is some improvement in uniform corrosion resistance
attributable to the Sn.
[0032] Bismuth, also an α-stabilizer in zirconium, has received little attention from the
nuclear materials community. It has been discovered in the present invention that
when bismuth, or a combination of bismuth and tin are used in a zirconium-based alloy,
two advantages are realized. First, bismuth has an exceptionally low thermal neutron
cross-section, lower even than zirconium and tin, and much lower than most other elements
commonly alloyed with zirconium.
[0033] An additional advantage is obtained when bismuth is included in a zirconium-based
alloy. The presence of bismuth in alloys of this type improves resistance to nodular
corrosion. It was determined in corrosion tests performed leading to the present invention
that zirconium alloyed with only bismuth (or with a tin-bismuth mixture) would provide
adequate protection against nodular corrosion.
[0034] It has been discovered in the present invention that the addition of certain other
alloying elements to zirconium-bismuth and zirconium-tin-bismuth alloys produces alloys
possessing acceptable uniform corrosion rates as well as improved resistance to nodular
corrosion. More specifically, the addition of an element or mixture of elements,
termed collectively herein as a solute portion of the alloy, selected from the group
consisting of niobium, tellurium and molybdenum, making up about 0.5-1.0% by weight,
or if tellurium alone is used, making up about 0.3-1% by weight of an alloy also
containing about 0.5% to 2.5% by weight of bismuth, or in the alternative containing
about 0.5 to 2.5% by weight of a tin-bismuth mixture, the balance being zirconium,
produces alloys which show substantial improvement in nodular corrosion resistance
compared to that of Zircaloy 2. In addition to providing improved resistance to nodular
corrosion, alloys having compositions in these ranges also possess the other desired
features previously mentioned;
i.e., low thermal neutron cross-section, and acceptable cost and ease of alloying. These
alloys will also contain the conventional impurities found in sponge zirconium and
zirconium alloys.
[0035] It should be noted that, in addition to the specified elements and conventional
impurities, the alloys of the present invention will also optionally contain from
about 0.09 to 0.16 weight percent of oxygen. Most commercial grade sponge zirconium
which would be used in making alloys such as the ones in the present invention will
contain small amounts of oxygen, roughly on the order of about 800-1300 parts per
million. In some instances, it will be desirable to increase the concentration of
oxygen in the alloy. Adding oxygen is one way to increase room temperature yield
strength. Thus, the alloys of the present invention may be produced with or without
the addition of oxygen, as this will have little or no effect on the corrosion resistance
of the alloys.
[0036] Tests for both uniform corrosion resistance and nodular corrosion resistance have
been conducted on alloys of the present invention. These tests have shown that a dramatic
decrease in susceptibility to nodular corrosion can be attained in an alloy which
is relatively insensitive to heat treatment, while retaining essentially the same
uniform corrosion resistance of Zircaloy 2.
[0037] The alloying elements which make up the solute portion are most effective in these
alloys at a total solute concentration of about 0.6-0.7 weight percent of the alloy.
Solute concentrations ranging from as low as about 0.3 weight percent (when tellurium
alone is used) to as high as about 1.0 weight percent have been tested and have been
shown to exhibit superior resistance to nodular corrosion, compared to the performance
of Zircaloy 2.
[0038] Table 1 lists several alloys which employ bismuth alone is on α-stabilizing element
and one alloy which employs a tin-bismuth mixture as stabilizing elements, with various
solute combinations in accordance with the present invention, along with three entries
at the bottom of the table which are Zircaloy 2 alloys in three (3) different heat
treatment states. These alloys were tested in water containing 8 ppm oxygen, at 288°C
and 1500 psig, conditions similar to a reactor operating temperature and pressure
(minus a radiation source), to evaluate the resistance of these alloys to uniform
corrosion.
[0039] It can be seen from the results in this table that the tested alloys of the present
invention exhibited adequate resistance to uniform corrosion. Some of these alloys
equalled or bettered the excellent performance of the Zircaloy 2 alloys. None of the
specimens tested under these conditions exhibited any sign of the formation of nodular
corrosion products.
[0040] Table 2 reports the results of tests conducted to determine the susceptibility to
nodular corrosion of alloys containing zirconium, bismuth, and a solute according
to the present invention. Tests were conducted on samples of the alloys in the as-cast
form with no special heat treatment as well as on samples which were annealed at 750°C
for 48 hours. This heat treatment, as previously mentioned, is one which essentially
strips the Zircaloy 2 alloy of its resistance to nodular corrosion in the laboratory
steam tests. Additional tests were conducted on samples in which cast buttons were
cold rolled to a 0.1 inch thickness and subsequently heat treated at either 750°C
for 48 hours or at 920°C for three hours.
[0041] Table 3 reports the results of tests performed to determine the susceptibility to
nodular corrosion of alloys containing zirconium, a mixture of bismuth and tin, and
a solute according to the present invention. These tests were conducted on samples
of the alloys in plate form (0.1 inch thickness). The alloys were tested in both a
cold-worked state, that is, no heat treatment being performed subse quent to the
plate-rolling procedure, and an annealed state wherein the samples were annealed at
750°C for 48 hours after being rolled into plate.
[0042] The test conditions used in Tables 2 and 3 (steam at 510°C, 1500 psig) were those
which induce, in the laboratory, the formation of the nodular corrosion product on
Zircaloy alloys (with a 750°C/48 hour anneal) like that found on Zircaloy alloys after
being used in reactor service. For purposes of comparison, the weight gains seen
in the annealed Zircaloy (not tabulated herein) under these same test conditions are
on the order of several thousand milligrams per square decimeter.
[0043] The results reported in both Table 2 and Table 3 show that the alloys of the present
invention undergo weight gains which are far superior to the weight gains evidenced
in the annealed Zircaloy alloys. Most of the results were lower than 200 mg/dm², compared
to the several thousand mg/dm² mentioned previously for the Zircaloy alloys. Additionally,
with only one exception noted by an asterisk (*) in the table, the alloys of the present
invention showed no sign of the formation of nodular corrosion products.
[0045] While other modifications of this invention and variations thereof which may be employed
within the scope of the invention have not been described, the invention is intended
to include such that may be embraced with the following claims.
1. A corrosion-resistant alloy consisting essentially of 0.5 to 2.5 weight percent
of bismuth, 0.5-1.0 weight percent of a solute composed of a member selected from
the group consisting of molybdenum, tellurium, niobium and mixtures thereof; and the
balance zirconium.
2. A corrosion-resistant alloy according to Claim 1 wherein the amount of solute is
substantially 0.6 weight percent.
3. A corrosion-resistant alloy according to Claim 1 wherein the amount of bismuth
is in the range 0.7-2.0 weight percent.
4. A corrosion-resistant alloy according to Claim 2 wherein the amount of bismuth
is in the range 0.7-2.0 weight percent
5. A corrosion-resistant alloy consisting essentially of 0.5 to 2.5 weight percent
of a mixture of tin and bismuth, 0.5-1.0 weight percent of a solute composed of molybdenum,
tellurium, niobium and mixtures thereof; and the balance zirconium.
6. A corrosion-resistant alloy according to Claim 5 wherein the amount of the mixture
of tin and bismuth is in the range of 2.0 to 2.2% by weight.
7. A corrosion-resistant alloy according to Claim 5 wherein the amount of the solute
is substantially 0.6% by weight.
8. A corrosion-resistant alloy according to Claim 6 wherein the amount of the solute
is substantially 0.6% by weight.
9. The corrosion-resistant alloy of Claim 1 further consisting essentially of 0.09
to 0.16% by weight of oxygen.
10. The corrosion-resistant alloy of Claim 5 further consisting essentially of 0.09
to 0.16% by weight of oxygen.
11. A corrosion-resistant alloy consisting essentially of 0.5 to 2.5 weight percent
of bismuth, 0.3-1.0 weight percent of a solute composed of tellurium; and the balance
zirconium.
12. A corrosion-resistant alloy according to Claim 11 wherein the amount of bismuth
is in the range 0.7-2.0 weight percent.
13. The corrosion-resistant alloy of Claim 11 further consisting essentially of 0.09
to 0.16% by weight of oxygen.
14. A corrosion-resistant alloy consisting essentially of 0.5 to 2.5 weight percent
of a mixture of tin and bismuth, 0.3-1.0 weight percent of a solute composed of tellurium;
and the balance zirconium.
15. A corrosion-resistant alloy according to Claim 14 wherein the amount of the mixture
of tin and bismuth is in the range of 2.0 to 2.2% by weight.
16. The corrosion-resistant alloy of Claim 14 further consisting essentially of 0.09
to 0.16% by weight oxygen.
17. A corrosion-resistant alloy according to Claim 3 wherein the solute is composed
of niobium and molybdenum, the amount of niobium being substantially 0.5% by weight
and the amount of molybdenum being substantially 0.5% by weight of the alloy.
18. A corrosion-resistant alloy according to Claim 4 wherein the solute is composed
of niobium and molybdenum, the amount of niobium being substantially 0.3% by weight
and the amount of molybdenum being substantially 0.3% by weight.
19. A corrosion-resistant alloy according to Claim 4 wherein the solute is composed
of niobium and tellurium the amount of niobium being substantially 0.3% by weight
and the amount of tellurium being substantially 0.3% by weight.
20. A corrosion-resistant alloy according to Claim 4 wherein the solute is composed
of molybdenum, tellurium and niobium, the amount of each being substantially 0.2%
by weight.
21. A corrosion-resistant alloy according to Claim 8 wherein the solute is composed
of niobium and molybdenum, the amount of niobium being substantially 0.3% by weight
and the amount of molybdenum being substantially 0.3% by weight.
22. A corrosion-resistant alloy according to Claim 8 wherein the solute is composed
of niobium and tellurium, the amount of niobium being substantially 0.3% by weight
and the amount of tellurium being substantially 0.3% by weight.
23. A corrosion-resistant alloy according to Claim 8 wherein the solute is composed
of molybdenum, tellurium and niobium, the amount of each being substantially 0.2%
by weight.