[0001] This invention relates to a method of making powder compacts.
[0002] Powdered metal compacts have been used in some industrial applications, but have
not generally found full acceptance because the extra method steps and the added cost
required to obtain a reasonable strength level and density in the powdered metal compact
have been excessive-, particularly when compared to similar parts obtained by melt
formation.
[0003] The conventional commercial mode of processing powdered metal to form compacts typically
comprises (a) blending and milling together selected ponder elements in the presence
of a lubricant, (b) compacting the mechanicelly blended charge (c) heating the compact
under a reducing atmosphere for a period of 30 min. at 810°C to volatilize the lubricant,
and (d) sintering the compact at an appropriate temperature. This has resulted at
best in a green density prior to sintering of about 79-86% and a sintered density
of 80-89% of theoretical. A higher density level would require additional hot forging
to increase the strength level and reduce porosity.
[0004] In order to increase the strength and aensity of the parts witnout secondary consolidstion
(hot forging), it has been proposed to effect cold briquetting or cold compacting
with a low melting matrix element effective to close pores; this processing is then
followed by conventional sintering (U.S. Patents Nos. 1,922,548 and 1,793,757 disclose
such proposals). Another method is to raise the temperature of the blended powders
to a liquid-solid condition and then sinter such powders in such multiphase condition
while under pressure. This is exemplified in U.S. Patent 3,393,630. The principal
difficulty that is experienced with cold briquetting is that it promotes a negative
effect on density even when low melting filler agents are employed. The principal
difficulty of sintering under pressure while in the liquiu-solid condition without
any pre-compaction is that the equipment is severely stressed and subjected to considerable
wear resulting in increased cost of processing.
[0005] According to the present invention, there is provided a method of producing a metal
powder compact which comprises compacting metal powder in the presence of from 1 to
5% by weight of a low-melting point metal at a temperature sufficient to melt , the
low-melting point metal.
[0006] In the preferred embodiment of the invention, 1-5%, preferably 2-4% of a low melting
metal ingredient (preferably selected from copper-tin, copper-lead, and lead) is added
to a coarse or fine iron powder and the mixture is subsequently warm- briquetted (preferably
at a temperature of 450-650°F) to form a liquid phase of said addition agent while
consolidating the powder. The particle size of the base iron powder is preferably
relatively fine (4-5 microns) and about 2.5% of a liquid phase promoting ingredient,
particularly tin, is preferably added thereto, the blended mixture has warm briquetted
at a temperature of from 450 to 650°F. The compact may then be sintered. Desirably
a cryogenically-produced fine powder is used as the source of the powdered metal.
[0007] The present invention includes two preferred embodiments:-(I) the addition of 1-5%
of a low-melting metal, such as which results, after warm briquetting, in a compact
having 25% less porosity and increased strength compared with a conventional cold
briquetted compact; and (II) the adaition of 1-5% of a low melting metal, such as
tin or lead, to a fine particle sizeiron powder, which results, after warm briquetting
and sintering, in a product having only 3% porosity compared with 20% porosity when
tin or lead is not used. The unprecedented strength and density level of the warm
briquetted compact makes it possible to produce certain powder metal parts without
sintering, resulting in significant energy savings. Candidate parts would be heat
sinks (such as diodes) and steering column collars. With respect to the 97% dense
sintered powder product, it can be produced with existing equipment (no forging) which
represents a major potential for a new class of powder metal business.
[0008] A preferred method for carrying out the first aspect of this invention is as follows:
(1) An iron powder is prepared preferably by water atomization which may have either
a coarse or a fine particle configuration. If a coarse configuration is employed,
the average particle size should be in the range of 80-100 microns and if a fine particle
size configuration is used, the average particle size should be about 4-5 microns.
When the powder is produced by water atomization, the chemical content of the powder
will typically consist of 99.8% Fe, 0.05%C, 0.04% Mn, and .035 Si. Since the water
atomization technique will require subsequent grinding and screening, the ultimate
product from this production cycle will result in a screen analysis such as 20% coarse,
60% fine, and 20; ultrafine. The particle size of the powder to be used herein should
preferably be uniform but may be a blend of coarse and fine particle configurations
provided the ratio is within the range of or less. If other powder making techniques
are employed, such as tie carbonyl process, the particle size range and chemistry
will be affected.
(2) The selected and sized iron powder is dry impact coated with a low-melting metal
selected from the group consisting of tin, copper-tin, lead, and copper-lead. One
preferred method for carrying out this dry impact coating is by use of a ball milling
apparatus employing large impact or milling balls consisting solely of the low-melting
metal, such as tin. The powder is placed preferably in a ball milling machine for
purposes of the trials herein, an interior chamber of 8" high x 8" in diameter was
used). Tin laden milling elements, preferably in the form of solid tin balls of about
.5" diameter, may be used. The powder charge was about 10 cubic inches and the milling
time about 48 hours. Milling time and the milling rate depend upon mill volume, mill
diameter, size of the tin balls, and the speed of rotation. The ball milling elements
should have a diameter at least 50 times the largest dimension of any of the particle
shapes of the powder.
[0009] The function of this step is to transfer, by impact, a portion of the tin ingredient,
carried by the ball milling elements, to form a tin shell about substantially each
particle of the powder. The coating is generated by abrasion or scratching of the
powder particle against the surface of' the ball milling elements. This obviously
is accomplished by rotating the housing of the ball mill machine to impart a predetermined
abrading force from the balls. The ball milling operation will cold work or generate
defect sites in substantially all of the powder particles above 124 microns; since
the majority of the particles selected for the process will be below said size range,
they will generally be free of cold work or defect sites. Theball milling operation
should be carried sufficiently long so that substantially each particle will be fully
coated; this requires statistically a minimum period of time so that tin coating will
preferably be continuous. When this step is completed, the particles will be in a
condition where they will all substantially have a continuous tin envelope (coating
or shell). Although the shell should preferably be an impervious continuous envelope
about each particle, it is not critical that it be absolutely impervious.
[0010] (3) The dry impact coatediron particles are then subjected to a heating treatment
while an agglomerating pressure is applied. Heat is applied to raise the temperature
of the mass of particles to a level slightly above the melting temperature of the
metal coating, whichsbould be in the range of 450-650 F, 419°F being necessary to
melt pure tin, 446°F being necessary to melt an alloy of 99.6% tin and .4% copper,
a melting temperature of 594°F is necessary to melt an alloy of 95% lead and 5% tin,
and a melting temperature of 561°F is necessary to melt an alloy of 63% tin and 37%
lead and a melting temperature of 618°F is necessary to melt pure lead. The warm briquetting
temperature could be mised to as much as 1350°F (723°C) if necessitated by the requirement
to melt the metal coating, or to improve densification by plastic deformation 450-1358°F
encompass warm briquetting herein. The pressure applied shoulu be no more than 30
tsi (and preferably in the range of 10-30 tsi) so that wear on the tooling used for
agglomeration is reduced to a minimum. Agglomerition or compaction may be-carried.
out by a conventional press to obtain the maximum desired densities herein. Compact
densities herein are considerably improved to 80% or more of theoretical density.
The presence of the solie tin or low melting envelope about the particles inproves
conpressibility acting as a lubricant, and the liquified metal phese acts as a pore
filler during the compaction operation. With prier uncoated powders, a density of
about 82% of theoretical or 6.4 gr. per cubic centimeter is typically obtained using
a compressive force of about 30 tsi; with a dry impact coated pewder herein densities
of about 7.0 gm. per cubic centimeter can be obtained at the same force level.
[0011] (4) The application of heat and pressure is removed al- lesing the low-melting metal
to solidify and form an auxiliary bend between the particles in addition to the normal
compressive and mechanical interlocking bond therebetween. Test results of this kind
of a warm briquetted product shows that it can be subjected to a hardness test evidencing
a Rockwell value of about R
B45. Moreover, a special bend test for such a product will show that it has a strength
level of at least 2000 psi, which is 400% greater than that of a product produced
without the use of the low-melting metal lubricant.
[0012] with respect to the second aspect of this invention, the first method is varied in
either or both of two respects. First, the iron powder selected is limited to a fine
particle size, averaging 4-5 microns. This can preferably be obtained by extracting
the iron powder as a by-product of processing of scrap or machining chips from industrial
metal work. To this end, scrap metal in the form of machine turnings are segregated
or selectad. Machine turnings are segments of ribbons of low carbon or alloy steel;
the turnings should be selected to have a surface to volume ratio of at least 60:1.
The machine turnings may be shavings cut from alloy bar, and the bar may have a chemistry
which includes alloying ingredients such as manganese, silicon, chromium, nickel and
molybdenum. The turnings will have a size characterized by a width of .1-1.0", thickness
of .005-.03"m and a length of 1-100". Machine turnings are usually not suitable for
melting in an electric furnace because they prevent efficient melt down due to such
surface to volume ratio. The turnings should be selected to be generally compatible
in chemistry when in the final product; this is achieved optimally when the turnings
are selected from a common machining operation where the same metal stock was utilized
in forming all the turnings.
[0013] The selected scrap pieces are put into a suitable charging passage leading to a ball
milling machine (or equivalent impacting device). within the passage means, an ingredient
for freezing the metal pieces is introduced, such as liquid nitrogen; it is sprayed
directly onto the metal pieces. Mere contact of the liquid nitrogen with the scrap
pieces will freeze them instantly. The liquid nitrogen should be applied uniformly
throughout its path to the point of impaction. The ballnilling elements are motivated
preferably by rotation of the housing to contact and impact the frozen pieces of scrap
metal causing them to fracture and be comminuted. Such impaction is carried out to
apply a sufficient fracturing force for a sufficient period of time and rate to reduce
said scrap pieces to a powder form. The resulting powder will be layered or flake
in configuration and typically have both coarse and fine powder proportions. A typical
screen analysis for a cryogenic powder would be as follows (for a 100 gm. sample):

[0014] Secondly, the method is varied in another important aspect: the compact or briquetted
product is subjected to sintering. This treatment can be carried out in a conventional
sintering furnace with heating to a temperature preferably about 2000°F. The temperature
to which the briquetted or compact is heated should be at least to the plastic region
for the metal constituting the powder. A controlled or protective atmosphere may be
maintained in the furnace, preftrably consisting of inert or reducing gases.
[0015] Whith sintering, a final density of about 97% has been achieved without the necessity
for secondary consolidation such as forging. This is an extremely high density for
a process which is essentially two step and devoid of secondary consolidation. Since
the compact does not contain a volatile lubricating agent, such as Acrowax, the delubrication
step is eliminated from the process or from the zone in a sintering furnace. The resulting
mechanical properties for such a sintered product would be as follows: tensile strength
115,000 psi, % elongation 10%, and hardness R
B78.
[0016] Test results to support the above methods are depicted in Table I. In one test example,
an iron powder specimen identified as Atomet 28 was employed which has a chemistry
of 99.8% Fe 0.05%C and an average particle size of 70-80 microns. The second powder
specimen consisted of carbonyl powder, having a chemistry of 99.9% Fe 0.1%C and a
particle size range of 4-5 microns. Each of the powders were subjected to dry impact
coating according to the step (2) described in the preferred method. Tin was employed
in amount of 2.5% weight percentage of the powder mass. This required ball milling
to be carried out for a period of 48 hours to achieve a coating thickness of about
0.1 micron. Each powder specimen was heated to a temperature level of 473°F. Density
measurements were obtained and compared with the same powder specimen but uncoated
and prepared according to a conventional technique using a 1% Zinc Stearate admixed
lubricant.

Although percentages of tin above 5% can be employed and will oporably work within
the system as described, it is suggested that more than 5% tin is not desirable because
of economic reasons, tin being considerably more expensive than iron. Also certain
physical characteristics are affected by the presence of large amounts of tin in the
resulting proauct. It is important to point out that the use of tin by itself without
the warm temperature to effect the liquid phase will create a negative effect on density.
[0017] The variation of density as a function of the percentage of tin employed is shown.
It increases for those compacts which are produced with warm compaction at a temperature
of about 473°F (245°C), the tin being in a liquid form during the compaction. Use
of 2.5 or 5% tin in the solid state reduces the density that can be obtained from
that achieved when tin is not present. It is therefor important to emphasize that
the use of a low-melting temperature metal additive is only effective when compaction
takes place with heat such that the additive is in liquid phase.
1. A method of producing a metal powder compact which comprises compacting metal powder
in the presence of from 1 to 5% by weight of a low-melting point metal at a temperature
sufficient to melt the low-melting point metal.
2. A method according to Claim 1 wherein the metal powder is compacted in the presence
of from 2 to 4%, by weight of the low-melting point metal.
3. A method according to Claim 1 or Claim 2 wherein the metal powder is compacted
at a pressure of less than 30 tons per square inch.
4. A method according to Claim 1 or Claim 2 wherein the metal powder is compacted
at a pressure of from 10 to 30 tons per square inch.
5. A method according to any one of Claims 1 to 4 wherein the metal powder is iron.
6. A method according to any one of Claims 1 to 5 wherein the low-melting point metal
is tin, a copper-tin alloy, a copper-lead alloy, or lead.
7. A method according to any one of Claims 1 to 5 wherein the low-melting point metal
is tin.
8. A method according to any one of Claims 1 to 7 wherein the metal powder is compacted
at a temperature of from 450 to 650°F.
9. A method according to any one of Claims 1 to 8 wherein the metal powder has a particle
size of from 60 to 120 microns.
10. A method according to any one of Claims 1 to 9 wherein the metal powder particles
are coated with the low-melting point metal prior to compacting.
11. A method according to Claim 10 wherein the coating is effected by dry-impact coating.
12. A method according to Claim 11 wherein the dry-impact coating is effected by ball
milling with milling elements composed of or carrying the low-melting point meatl.
13. A method according to Claim 11 wherein metal powder compact is sintered.
14. A method of making high density powdered metal compacts comprising adding 2-4%
by weight of a low-melting point metal to an iron powder supply having a uniform particle
size to form a mixture, and warm briquetting the mixture at a temperature effective
to melt the low-melting metal while employing a compacting pressure no greater than
30 T.s.i.
15. A method of making high density powdered metal compact, comprising:
(a) preparing a 99.8% pure iron powder having a uniform particle size of 60-120 microns,
(b) dry impact coating of the particles of prepared iron powder with a metal lubricating
agent constituting 1-5% by weight of said powder, said agent being characterized by
an ability to form a liquid phase in the temperature range of 450-650°F,
(c) heating said coated powder to said temperature range for forming a liquid phase
of said agent, while agglomerating said powder with a pressure of 10-30 tsi whereby
a compacted product is obtained having a theoretical density of at least 80%, a Rockwell
hardness of RB45, and a bend strength of 2000 psi.