Background of the Invention
[0001] This invention relates to a method for introducing a controlled level of oxygen into
agglomerated molybdenum metal powder and in particular, into agglomerated molybdenum
plasma spray powder.
[0002] Flame spraying and plasma spraying are common techniques for the application of protective
and wear resistant coatings of various metals, ceramics, and cermets, usually to metal
surfaces (substrates). The piston ring industry commonly uses molybdenum coating on
rings for internal combustion engines.
[0003] In the flame spraying technique an electric arc or an oxyacetylene flame melts the
end of a continuous coil of molybdenum wire and a gas propels it onto a substrate
for example, the war surface of a cast iron piston ring where it splats and solidifies,
forming the coating in successive layers. Because of the presence of excess oxygen
either from the flame or the surrounding air, or both, the coatings produced by this
technique contain large quantities of oxygen, typically from about 7% to about 8%
in solution and as various molybdenum oxides. The large quantities of oxygen in the
molybdenum apparently harden the coating.
[0004] In the plasma spraying of molybdenum, there is usually a minimum of oxygen in the
sprayed coating due to the use of an oxygen-lean plasma gas system. That is, argon,
helium, hydrogen, nitrogen, or combinations of these gases, all of which are relatively
free from oxygen, are used in the plasma spraying process. Hence, any oxygen in the
sprayed coating is incidentally due to oxidation of the molten particles by oxygen
impurity in the plasma gas and/or surface oxidation of the freshly deposited coating.
In such "pure" molybdenum coatings the oxygen level is in the 1% to 2% range. Such
coatings are softer than their flame sprayed counterparts.
[0005] For higher hardness, therefore, a more expensive process such as the flame spray
process which requires wire, or a more expensive powder such as molybdenum plus nickel-base
alloy must be used.
[0006] It would be desirable therefore to have a method of producing molybdenum powders
of sufficiently high oxygen content to enable them to be used in a plasma spray process
to produce hard coatings.
[0007] US Patent 4,146,388 describes and claims molybdenum plasma spray powders and a process
for producing the powders of molybdenum having an oxygen content of from about 0.5
to about 15% by weight oxygen. The process involves passing molybdenum particles through
a plasma with oxygen or oxides of molybdenum to produce the oxygen containing (oxidized)
powder.
Summary of the Invention
[0008] In accordance with a first aspect of this invention, there is provided a method for
introducing a controlled level of oxygen into agglomerated molybdenum metal powder,
involving contacting the powder with a relatively dilute solution containing a sufficient
amount of oxidizing agent for a sufficient time to increase the oxygen content of
the powder followed by removing the resulting partially oxidized powder from the resulting
solution.
[0009] In accordance with a second aspect of this invention, there is provided a method
for introducing a controlled level of oxygen into agglomerated molybdenum metal powder,
involving heating the powder at sufficient temperature for a sufficient time in the
presence of water vapor, and a non-oxidizing atmosphere with the amount of the non-oxidizing
atmosphere being controlled to produce a partially oxidized molybdenum powder.
[0010] In accordance with a third aspect of this invention, there is provided a method for
introducing a controlled level of oxygen into agglomerated molybdenum plasma spray
powder. The method involves forming a relatively uniform mixture of agglomerated powders
containing essentially of molybdenum and one or more oxygen containing compounds of
molybdenum wherein the mixture has an oxygen content of greater than about 10% by
weight and reducing the mixture at a sufficient temperature for a sufficient time
to remove a portion of the oxygen therefrom and form a molybdenum powder having an
oxygen content of no greater than about 10% by weight.
Brief Description of the Drawing
[0011] Figure 1 is a plot of nitrogen flow rate versus weight percent oxygen in the oxidized
molybdenum powder (second aspect of the invention).
Detailed Description of the Invention
[0012] For a better understanding of the present invention, together with other and further
objects, advantages and capabilities thereof, reference is made to the following disclosure
and appended claims in connection with the above described drawing and description
of some of the aspects of the invention.
[0013] In particular applications in which the controlled oxygen molybdenum powders resulting
from the method of this invention are preferably used, that is, in plasma spray applications,
the desired oxygen content is from about 1% to about 15% and preferably from about
7% to about 10% by weight. At levels lower than this, the hardness of the plasma coating
is not improved. At levels higher than this range, coating integrity or bond strength
is compromised.
[0014] US Patent 4,146,388 discloses a process for producing molybdenum spray powders containing
oxygen by the plasma melting process or in conjunction with the plasma melting process.
By the process of this invention the oxygen level in molybdenum powders is controlled
in preparation for plasma coating applications.
[0015] In the practice of this invention, the molybdenum powder has been previously agglomerated
and sintered by well known methods.
[0016] One preferred method of agglomerating the molybdenum powder is described in US Patent
3,973,948. Methods are disclosed also in a paper entitled "Properties of Oxygen-Bearing
Molybdenum Coating," published in the proceedings of the Ninth International Thermal
Spray Conference, The Hague, Netherlands, May 19-23, 1980.
[0017] The preferred molybdenum powder of this invention is supplied by the Chemical and
Metallurigcal Division of GTE Products Corporation under the designation SA-101.
[0018] By the method according to the first aspect of this invention, the oxygen content
of conventional molybdenum powders which preferably consist essentially no greater
than about 0.05% by weight oxygen can be increased by contacting the powder with a
relatively dilute solution containing a sufficient amount of an oxidizing agent, which
is preferably hydrogen peroxide for a sufficient time to raise the oxygen content
to the desired level. The oxidizing agent must be present in a sufficient amount to
raise the oxygen to the desired level, but not in excess amounts to cause the reaction
to be uncontrolled.
[0019] A dilute solution of the oxidizing agent affords better control and avoids excessive
oxidized The solution contains preferably from about 1% to about 10% by weight of
the oxidizing agent.
[0020] By controlling the contact time, amount and dilution of the oxidizing solution, and
the ratio of the molybdenum to the oxidizing agent, the oxidation can be controlled.
[0021] It is the preferred practice, when using hydrogen peroxide, to have from about 2
to about 5 moles of the oxidizing agent present per mole of molybdenum.
[0022] The resulting partially oxidized molybdenum powder is then separated from the resulting
solution by any standard technique such as filtration.
[0023] To more fully illustrate this first aspect of the invention, the following non-limiting
example is presented.
Example
[0024] About 7 grams of molybdenum powder type SA-101 from GTE which has been spray dried
and which is -200, +325 mesh and containing about 0.2% by weight oxygen is contacted
with a solution consisting essentially of about 6 cc of 30% hydrogen peroxide in about
150 cc of deionized water for about 2 hours. The resulting partially oxidized molybdenum
powder is then filtered off and dried. Analysis of this powder shows an oxygen content
of about 1.8% by weight.
[0025] By the method according to the second aspect of this invention, the oxygen content
of conventional molybdenum powders which preferably consist essentially of less than
about 0.05% by weight oxygen can be increased by heating the agglomerated and sintered
powder at a sufficient temperature for a sufficient time in the presence of water
vapor and a non-oxidizing atmosphere with the amount of the non-oxidizing atmosphere
being controlled to produce a partially oxidized molybdenum powder.
[0026] The heating can be done by any standard method for heating metal powders.
[0027] Preferred methods involve the use of a rotary calciner or a fluidized bed.
[0028] Heating temperatures are generally from about 700°C to about 900°C with from about
750°C to about 850°C being preferred.
[0029] The heating time depends on the temperature and on the type of equipment used. For
example, the slope of the calciner tube can be adjusted to vary the length of time
that the powder remains in the calciner.
[0030] Water is introduced into the furnace to provide the necessary moisture for the process.
[0031] The preferred non-oxidizing atmosphere is nitrogen. By controlling the amount of
non-oxidizing atmosphere in the ambient atmosphere of the furnace, the degree of oxidation
or the oxygen content of the molybdenum powder is controlled. The amount of the non-oxidizing
gas can be controlled by controlling the flow rates. It has been found, for example,
that when the flow rate of the non-oxidizing atmosphere, for example, nitrogen, is
decreased, the oxygen content of the resulting partially oxidized molybdenum is increased.
This will be apparent in the example that follows.
[0032] The resulting partially oxidized molybdenum powder is made up of essentially spherical
particles. The oxygen content of this powder ranges from about 3% to about 15% by
weight.
[0033] X-ray analyses of the partially oxidized power generally shows molybdenum trioxide.
Undesirable molybdenum trioxide can be eliminated by using ammonia solution to dissolve
it without disturbing other desirable properties of the powder.
[0034] Also, in the event that the oxygen content is too high, the powder can be subjected
to standard reduction methods to reduce the oxygen content.
[0035] To more fully illustrate this second aspect of the invention, the following non-limiting
example is presented.
Example
[0036] Molybdenum powder type SA-101 from GTE which has been spray dried and which is -200,
+325 mesh (44 to 74µm) is fed at the rate of about 12 pounds (5.4 kg) per hour into
a 6" (152.44 mm) diameter rotating calciner at a temperature of about 800°C under
a nitrogen atmosphere. Water is fed by a separatory funnel at the rate of about 20
to 30 cm³/min to provide the necessary moisture for the oxidation process. The resulting
powder is in the form of essentially spherical brown particles with a bulk density
of from about 2.4 to about 2.8 g/cm³.
[0037] The above procedure is carried out with the flow rate of the nitrogen being varied.
[0038] The oxygen contents of the resulting powders are given below along with the flow
rates of the nitrogen.

[0039] A plot of the nitrogen flow rate versus weight percent oxygen in the resulting powder
is shown in Figure 1.
[0040] It can be seen that a direct correlation exists between the flow rate of the nitrogen
and the percent oxygen in the oxidized powder. As the nitrogen flow rate decreases,
the degree of oxidation as shown by the weight percent oxygen increases.
[0041] With regard to the third aspect of the present invention, the oxygen containing compounds
of molybdenum can be molybdenum dioxide, molbydenum trioxide, or ammonium paramolybdate.
[0042] It is to be understood that any mixture of molybdenum and oxygen containing compounds
of molybdenum can be used as long as the oxygen content of the agglomerated mixture
is greater than about 10% by weight.
[0043] A typical composition of the mixture of molybdenum powders to be agglomerated consists
essentially of in percent by weight about 40% molybdenum, about 50% molybdenum dioxide,
and about 10% molybdenum trioxide with the oxygen content being about 15.8% by weight.
[0044] The mixture of molybdenum and the oxygen containing compound or compounds can be
agglomerated by any of several methods well known in the art.
[0045] Within the third aspect of the invention, a preferred method involves generally forming
a slurry of water, ammonia or ammonium hydroxide, molybdenum trioxide, molybdenum
dioxide, and ultrafine (about 1 to 3 microns in diameter) molybdenum particles. Ammonium
paramolybdate is formed from the molybdenum trioxide and ammonium hydroxide and acts
as the binder in this system. The resulting slurry is then spray dried to remove the
water and form the relatively uniform agglomerated mixture which consists of essentially
spherical particles. The above method of forming the agglomerated mixture is described
in US Patent 3,973,948 which is hereby incorporated by reference.
[0046] Another method of forming the relatively uniform agglomerated mixture is by first
forming a slurry as described above. The water is allowed to evaporate while the slurry
is being continually stirred to break up the material. The resultant coarse moist
powder is then forced through a 100 mesh screen and collected. The powder is then
further dried with gentle agitation. The final agglomerated mixture is then screened
from this dried mixture.
[0047] Some preferred methods of agglomerating the molybdenum powder are disclosed in the
above-mentioned paper entitled "Properties of Oxygen-Bearing Molybdenum Coatings,"
published in the proceedings of the Ninth International Thermal Spray Conference,
The Hague, Netherlands, May 19-23, 1980.
[0048] In accordance with the third aspect of the invention, the resulting agglomerated
mixture is then reduced at a sufficient temperature for a sufficient time to remove
a portion of the oxygen and form a molybdenum powder having an oxygen content of no
greater than about 10% and preferably from about 7% to 10% by weight.
[0049] The reduction can be done in a standard furnace in a dry hydrogen atmosphere. The
preferred temperatures are from about 700°C to about 1000°C. The time depends on the
temperature and on the nature of the equipment. However, typical times are from about
2 hours to about 4 hours.
[0050] The reduction can be done in a fluidized bed or rotary calciner. The reducing conditions
are adjusted to give the final desired oxygen content. The advantages of using a fluidized
bed or rotary calciner over the above described static bed reduction are that a bed
depth problem is avoided resulting in a more uniform reduction than in the static
bed furnace. In a fluidized bed or rotary calciner the reduction of the agglomerate
takes place from the outside of the agglomerates to the inside resulting in the metal
phase being on the outside of the agglomerates. This results in a more efficient melting
of the agglomerates in the plasma application and therefore produces a harder coating.
[0051] The resulting powders with controlled oxygen levels are used in plasma spraying applications
to produce coatings such as on piston rings.
[0052] To more fully illustrate the third aspect of this invention, the following non-limiting
example is presented. All parts, portions, and percentages are on a weight basis unless
otherwise stated.
Example
[0053] An aqueous slurry is made up consisting essentially of about 85% solids, the solids
consisting essentially of about 11% molybdenum trioxide, about 52% molybdenum dioxide,
and about 36% molybdenum, the oxygen content of the solids being about 16.6%, and
ammonia in an amount equal to about 87% of the molybdenum trioxide. The slurry is
dried in a conventional dryer to produce a relatively uniform agglomerated mixture
consisting of particles which are essentially spherical in shape. The mixture is reduced
in dry hydrogen at about 800°C for about 2 hours resulting in a free-flowing molybdenum
spray powder having an oxygen content of from about 7% to about 8%.
[0054] While there has been shown and described what are at present considered the preferred
embodiments of the three aspects of the invention, it will be obvious to those skilled
in the art that various changes and modifications may be made therein without departing
from the scope of the invention as defined by the appended claims.
1. A method for introducing a controlled level of oxygen into agglomerated molybdenum
metal powder, said method comprising
a) contacting said powder with a relatively dilute solution containing a sufficient
amount of an oxidizing agent for a sufficient time to increase the oxygen content
of said powder; and
b) removing the resulting partially oxidized powder from the resulting solution.
2. A method of claim 1 wherein said powder is contacted with a solution consisting
essentially of in percent by weight from about 1% to about 10% of said oxidizing agent
with from about 2 moles to about 5 moles of said oxidizing agent being present per
mole of molybdenum.
3. A method of claim 2 wherein said oxidizing agent is hydrogen peroxide.
4. A method for introducing a controlled level of oxygen into agglomerated molybdenum
metal powder, said method comprising heating said molybdenum powder at a sufficient
temperature for a sufficient time in the presence of water vapor, and a non-oxidizing
atmosphere with the amount of said non-oxidizing temperature being controlled to produce
a partially oxidized molybdenum powder.
5. A method of claim 4 wherein the temperature is from about 700°C to about 900°C.
6. A method of claim 5 wherein said non-oxidizing atmosphere is nitrogen.
7. A method of claim 6 wherein the oxygen content of said partially oxidized molybdenum
powder is from about 3% to about 15% by weight.
8. A method for introducing a controlled level of oxygen into agglomerated molybdenum
plasma spray powder, said method comprising:
a) forming a relatively uniform mixture of agglomerated powders consisting essentially
of molybdenum, and one or more oxygen containing compounds of molybdenum wherein said
mixture has an oxygen content of greater than about 10% by weight; and
b) reducing said mixture at a sufficient temperature for a sufficient time to remove
a portion of the oxygen therefrom and form a molybdenum powder having an oxygen content
of no greater than about 10% by weight.
9. A method of claim 8 wherein said mixture consists essentially of molybdenum, ammonium
paramolybdate, and molybdenum oxides.
10. A method of claim 8 wherein the reducing temperature is from about 700°C to about
1000°C.
11. A method of claim 10 wherein the oxygen content of the reduced molybdenum powder
is from about 7% to about 10% by weight.