GB2045280A - Liquid Phase Sintering Iron- carbon Alloys - Google Patents

Liquid Phase Sintering Iron- carbon Alloys Download PDF

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Publication number
GB2045280A
GB2045280A GB7910800A GB7910800A GB2045280A GB 2045280 A GB2045280 A GB 2045280A GB 7910800 A GB7910800 A GB 7910800A GB 7910800 A GB7910800 A GB 7910800A GB 2045280 A GB2045280 A GB 2045280A
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approximately
carbon
iron
alloy
blend
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GB7910800A
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GB2045280B (en
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Amsted Industries Inc
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Amsted Industries Inc
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Priority to GB7910800A priority Critical patent/GB2045280B/en
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C33/00Making ferrous alloys
    • C22C33/02Making ferrous alloys by powder metallurgy
    • C22C33/0207Using a mixture of prealloyed powders or a master alloy
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C33/00Making ferrous alloys
    • C22C33/02Making ferrous alloys by powder metallurgy
    • C22C33/0257Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
    • C22C33/0278Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
    • C22C33/0285Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5% with Cr, Co, or Ni having a minimum content higher than 5%

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Powder Metallurgy (AREA)

Abstract

High carbon high density iron based alloys containing at least 1% Cx, U, Mo, W is made by atomising an iron based alloy melt containing <0.2% C and then adding sufficient C to the atomised powder to widen the gap between the solidus and liquidus temperatures of the mix. The mix is then compacted and liquid phase sintered.

Description

SPECIFICATION Method of Producing High Density Iron-based Material Background and Summary of the Invention This invention relates to a method of producing a high density iron-base material. It is more particularly concerned with a powdered metal process for producing an iron-base alloy wherein the desired high density is achieved by liquid phase sintering.
For various reasons, some parts or articles must be made of a material having certain special properties. Often, the most desirable method of producing such parts is by powdered metal methods.
For example, parts or articles subjected to certain service conditions are preferably made of an alloy having a high wear resistance. Materials having the required wear resistance are generally extremely difficult or impossible to machine into the desired configuration. Generally, articles made of these alloys are produced in the form of castings and ground to the desired dimensions.
Casting of wear-resistant articles may be satisfactory for the production of relatively large parts, but it may be impractical or uneconomical for the production of smaller articles. Therefore, it is desirable to be able to produce such smaller articles by a powdered metal process.
In a powdered metal process of producing these articles, the high density required may be achieved by liquid phase sintering. That is, the compacted article is sintered at a temperature between the solidus and liquidus temperatures of the particular alloy being produced in order to achieve a density of nearly the full theoretical density of the material.
However, some alloys which have very desirable properties such as high wear resistance are substantially eutectic. That is, their solidus and liquidus temperatures coincide or are so nearly equal that it is impractical to control the sintering temperature accurately enough to sinter an article between the two temperatures. Therefore, economical commercial production by powdered metal methods of articles made of substantially eutectic materials has been virtually impossible heretofore.
It is therefore an object of the present invention to provide a method of producing a high density iron-base material by a powdered metal process that overcomes the difficulties encountered heretofore.
According to the present invention, this is accomplished by adding carbon particles to powders of a substantially eutectic alloy, thereby increasing the difference between the solidus and liquidus temperatures and facilitating liquid phase sintering.
Brief Description of the Drawing The drawing is a portion of the phase diagram in relation to carbon content for an iron-base alloy having a chromium content of about 17%.
Description of the Preferred Embodiment Phase diagrams show the temperatures within which various phases of an alloy are present and the boundaries at which phase changes occur. Referring to the drawing, the solidus and liquidus lines of an iron-base alloy having a chromium content of about 17% are shown from a carbon content of about 1% to about 5%. The solidus line represents the temperature below which all components of the particular alloy are in a solid phase. The liquidus line represents the temperature above which all components of the particular alloy are in a liquid phase. At temperatures between the solidus and liquidus lines some solid phase is present and some liquid phase is present.
The drawing shows that as the carbon content increases from about 1%, the solidus and liquidus lines converge until they meet at a point representing a carbon content of about 3.3% at a temperature of about 1 2200C. With further increase of carbon content, the lines rapidly diverge.
The point at which the solidus and liquidus lines meet is designated as the eutectic point. That is, if the alloy having the phase diagram as represented by the drawing has a carbon content of 3.3%, at a temperature below 1 220cm all components of the alloy will be in a solid phase, and at a temperature above 1 2200C all components will be in a liquid phase.
Under these conditions it is theoretically impossible to perform liquid phase sintering of an alloy that is eutectic because there is no difference between the solidus and liquidus temperatures. A temperature can be determined between the solidus and liquidus temperatures of an alloy having a carbon content that approaches the eutectic point. However, the width of the liquid phase sintering range of such an alloy might be so narrow that it would be economically impractical to control the sintering temperature accurately enough in a commercial production operation.
This would be true for the iron-base alloy of the drawing if the carbon content were between about 3 and 3.5%. At 3% carbon, the solidus temperature is about 1 2250C, and the liquidus temperature is about 1 2500C. Thus, the liquid phase sintering range is merely 250C, which is too narrow a sintering range for practical commercial production of powdered metal articles.
Applicant has discovered that by increasing the carbon content of a substantially eutectic cold compactible powdered metal iron-base alloy, the difference between the liquidus and solidus temperatures may be increased sufficiently to provide a liquid phase sintering range which facilitates economical commercial production. Preferably the carbon content is increased by blending the cold compactible powder with carbon particles to achieve a carbon content of about 1 to 2 percentage points above that normally found in the substantially eutectic iron-base alloy.For example, if cold compactible powder of a 3% carbon alloy having a phase diagram as represented by the drawing is blended with an additional 1% by weight of carbon particles, the solidus temperature of the blend will be about 121 00C and the liquidus temperature will be about 1 2700C. Thus, the width of the liquid phase sintering range has been increased from about 250C to about 600 C.
If 2% by weight of carbon particles is blended with cold compactible powder of the same alloy, the solidus temperature (at 5% carbon in the drawing) is now about 11 950C and the liquidus temperature is about 1 3450C. The width of the liquid phase sintering range has therefore been increased to about 1 500 C. Temperature ranges as broad as 60 or 1 500C can be controlled economically in a commercial production operation.
Moreover, it has been found that the additional 1 to 2% carbon by weight has little or no effect on the properties of the resulting alloy. That is, the new higher carbon alloy has essentially the same characteristics as the substantially eutectic alloy from which it was produced.
It should be noted that in the preferred method of producing the high density iron-base material, the cold compactible powder of the substantially eutectic iron-base alloy is obtained by atomizing a melt having the same composition as the substantially eutectic alloy except for carbon content. The melt preferably has a carbon content of less than 0.2%. The powder obtained is cold compactible and can be blended with carbon particles to obtain the cold compactible powder of the substantially eutectic alloy. The details and advantages of this process are described more completely in United States Patent No. 4,121,927.When employing this method of practising the present invention it should be noted that the desired result of broadening the liquid phase sintering range may also be accomplished by blending only enough carbon particles with the low carbon powder to obtain a blend having a lower carbon content than the eutectic alloy. That is, for example, if sufficient carbon particles were added to the low carbon powder to obtain a blend having a carbon content of only about 2%, the solidus temperature of the resulting alloy would be about 1 2400C and the liquidus temperature would be about 1 3450C. The resulting liquid phase sintering range, therefore, would be about 1 050C. As described above, a temperature range of 1 050C can be controlled economically in a commercial production operation.
According to the present invention, the cold compactible powder may be obtained in any other manner desired. For example, a melt of the substantially eutectic iron-base alloy, including carbon, may be atomized to produce a hardened powder that cannot be cold compacted. The hardened powder may be treated to render it suitable for cold compaction.
The following is an example of applying the preferred method of the present invention to the production of a high density wear resistant material. One iron-base alloy which is normally cast into products and which has good wear resistant properties comprises the following analysis by weight: Chromium About 17% Molybdenum About 16% Cobalt About 6% Carbon About 3% Vanadium About 1.9% Silicon About 1.5% maximum Manganese About 1% maximum Nickel About 0% Others About 3% maximum Iron Essentially balance At 3% carbon by weight, this alloy is substantially eutectic, but as the carbon content is increased above 3%, the solidus and liquidus temperatures diverge along lines in much the same manner as graphically illustrated by a solidus and liquidus lines of the drawing. However, the phase diagram of the drawing is not exactly the phase diagram of the alloy of this example. The alloy described above is available commercially and is known as Haynes Alloy &num;93.
A heat of this alloy except for the carbon content was water atomized and screened to provide a -88 mesh cold compactible powdered metal having the following analysis by weight: Chromium About 17% Molybdenum About 16% Cobalt About 6% Carbon About 0.2% maximum Vanadium About 1.9% Silicon About 1.5% maximum Manganese About 1% maximum Nickel About 0% Others About 3% maximum iron Essentially balance.
The powdered metal was blended with 4% by weight natural graphite to achieve the desired elevated carbon content. The blend of powdered metal and graphite was then cold compacted in a closed die at about 7025 kg/cm2 to form blanks about 2.5 cm in diameter and about .75 cm thick. The green blanks had a density of about 5.65 gm/cc, or about 72.7% of the theoretical density. Finally, the blanks were sintered in a vacuum at 11 650C for two hours.
It has been found that 99% theoretical density can be achieved with controllable dimensions using this method. The parts produced by this method have a wear resistance substantially equal to parts made of the eutectic cast Haynes Alloy &num;93.

Claims (9)

Claims
1. A method of producing a high carbon, heat- and abrasion-resistant and high density, ironbased alloy having a final composition which includes at least 1% of one or more of chromium, vanadium, molybdenum and tungsten, said method comprising the steps of: atomizing a melt having an initial carbon content of less than 0.2% to form a cold compactible powder of an iron-based alloy, blending a quantity of carbon particles with said powder to create a blend of powdered metal having a carbon content greater than the carbon content found at the eutectic point of said iron-based alloy so as to provide a greater difference between the solidus and liquidus temperatures than the difference normally present in a eutectic iron-based alloy, compressing said blend into a compacted blank in a die at a pressure in excess of 2800 kg/cm2, removing said compacted blank from said die and then sintering said compacted blank at a temperature between the solidus and liquidus temperatures of said blend to provide a high density material.
2. A method according to Claim 1, wherein said cold compactible powder has a composition of the following analysis: Chromium Approximately 17% Molybdenum Approximately 16% Cobalt Approximately 6% Carbon Approximately 0.2% maximum Vanadium Approximately 1.9% Silicon Approximately 1.5% maximum Manganese Approximately 1% maximum Nickel Approximately 0% Others Approximately 3% maximum Iron Essentially balance.
3. A method according to Claim 1 or 2, wherein said carbon particles comprise from 3.8% to 4.8% of said blend by weight.
4. A method according to Claim 1 or 2, wherein said carbon particles comprise approximately 3.8% of said blend by weight and said sintering is performed at about 11 650C for about two hours.
5. A method according to any one of the preceding claims, wherein said sintering is performed in a near vacuum.
6. A method of producing a high carbon heat- and abrasion-resistant and high density iron-based alloy, having a final composition which includes at least 1% of one or more of chromium, vanadium, molybdenum and tungsten, substantially as hereinbefore described with reference to either of the foregoing Examples, or with reference to the accompanying drawing.
7. A high carbon heat- and abrasion-resistant and high density iron-based alloy blank having a composition which includes at least 1% of one or more of chromium, vanadium, molybdenum and tungsten, when produced by a method as claimed in any one of the preceding claims.
8. An article made from a blank as claimed in Claim 7.
9. The features hereinbefore disclosed, or their equivalents, in any novel selection.
GB7910800A 1979-03-28 1979-03-28 Liquid phase sintering iron-carbon alloys Expired GB2045280B (en)

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GB2045280B GB2045280B (en) 1983-03-23

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995026421A1 (en) * 1994-03-25 1995-10-05 Brico Engineering Limited A method of making a sintered article
GB2301376A (en) * 1994-03-25 1996-12-04 Brico Eng A method of making a sintered article
GB2354256A (en) * 1999-09-15 2001-03-21 Korea Atomic Energy Res uranium high-density dispersion fuel

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995026421A1 (en) * 1994-03-25 1995-10-05 Brico Engineering Limited A method of making a sintered article
GB2301376A (en) * 1994-03-25 1996-12-04 Brico Eng A method of making a sintered article
GB2301376B (en) * 1994-03-25 1997-09-10 Brico Eng A method of making a sintered article
GB2354256A (en) * 1999-09-15 2001-03-21 Korea Atomic Energy Res uranium high-density dispersion fuel
GB2354256B (en) * 1999-09-15 2001-11-07 Korea Atomic Energy Res Uranium high-density dispersion fuel

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 19980328