US2464517A - Method of making porous metallic bodies - Google Patents

Method of making porous metallic bodies Download PDF

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US2464517A
US2464517A US486815A US48681543A US2464517A US 2464517 A US2464517 A US 2464517A US 486815 A US486815 A US 486815A US 48681543 A US48681543 A US 48681543A US 2464517 A US2464517 A US 2464517A
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crystals
metal
ingot
mesh
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Kurtz Jacob
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CALLITE TUNGSTEN Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/10Sintering only
    • B22F3/11Making porous workpieces or articles
    • B22F3/1143Making porous workpieces or articles involving an oxidation, reduction or reaction step
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • B22F2998/10Processes characterised by the sequence of their steps
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12021All metal or with adjacent metals having metal particles having composition or density gradient or differential porosity
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12153Interconnected void structure [e.g., permeable, etc.]

Definitions

  • the present invention relates to porous metallic bodies and methods of making the same. More particularly, it relates to porous metallic bodies suitable for use as filters and while the method may be used with a wide variety of metals, in its preferred form it is applicable to the formation of porous bodies of refractory metals such as tungsten and molybdenum. It has, however, a special adaptation to alloys such as iron molybdenum manganese alloy, and generally to metals that can be cast and suddenly chilled in a manner to produce a brittle formation of large crystals.
  • the method may generally be described as, first, forming an ingot or body of other shape having large crystals and a consequent brittleness of structure which permits the breaking up of the body into its component crystals.
  • the individual crystals are of considerable strength and hardness although the body as a whole formed from these crystals is quite brittle.
  • the body is first formed into large crystals either by heating the ingot in the case of the more refractory metals to the germinating temperature, or by casting the ingot and immediately chilling it.
  • the ingot is then broken up into its component crystals and these crystals are again broken down by mechanical means such as ball milling, crushing or hammering.
  • the crystal fragments so produced vary considerably in size and it is, therefore, desirable to screen the fragments into different batches in which the particles are of approximately equal sizes. This may be done by passing the powdered crystalline material through a series of screens varying from say 40 mesh to about 350 mesh. There may thus be screens of the following sizes which are given by way of example merely: 40 mesh, 60 mesh, 100 mesh, 150 mesh, 20'.) mesh, 250 mesh, 300 mesh, and 350 mesh. By combining the material retained on certain screens with that retained on others, a considerable degree of control of the porosity of the finished body is permitted.
  • a certain degree of porosity of the finished body may be secured, and this porosity may be increased by increasing the proportion of larger size fragments or it may be diminished by increasing the proportion of the smaller size fragments.
  • a batch When a batch is prepared having a predetermined proportion of large and small size fragments, it is thoroughly wetted with a solution of a soluble salt of a metal such as silver, copper or nickel.
  • the salt used should be one yvhich will break down to the oxide under temperature.
  • an aqueous solution of silver nitrate may be used and the powdered crystalline metal is thoroughly wetted with this solution and dried so as to form a coating of silver nitrate on the individual particles. It is then heated to a temperature sufficient to break down the nitrate tc the oxide.
  • a binding material which is decomposable at temperatures below sintering temperature, of the metal with which the powdered base metal is coated and which will volatilize at that temperature without leaving a residue, should be used.
  • binding materials are paraffin dissolved in carbon tetrachloride, salicyclic acid, naphthalene, benzyldichloride, and ammonium chloride, and many others.
  • the coated powdered metal is thoroughly mixed with this binding material and the mass is shaped in a die under hydraulic pressure.
  • the mass is then heated in an atmosphere of hydrogen to a temperature suificient to volatilize the binder out of the mass without leaving a carbon residue, and when volatilization is complete the temperature is held sufiiciently high to reduce the oxide coating to a metallic coating.
  • This temperature should be further increased to a point at which the coating metal on the particles will s'inter but it should not be sufficientlyhigh to melt the coating metal to a fluid condition at which it would flow off the particles.
  • There is very little shrinkage of the body under this treatment owing to the fact that at the temperatures used the crystalline fragments show little tendency to coalesce and the voids remaining after the volatilization of the binding material show practically no diminution of size or number. Nowithstanding this lack of shrinkage, the final product has considerable mechanical strength.
  • the method may be illustrated by describing the formation of such a body from tungsten.
  • Tungsten powder is first formed under hydraulic pressure in a die to the shape of a bar or ingot. This bar is then sintered and heat treated in a hydrogen atmosphere at the temperature of aspen-1,0 a l fore described, and the particles thus graded cording to size. Batches selected according to e are then thoroughly mixed together in a pretermined manner to produce the desired degree porosity in the finished body and the mass so .”med is thoroughly wetted with an aqueous lution of silver nitrate and then dried. Into e same so formed a solution of parafiin dislved in carbon teterachloride is thoroughly xed and dried, and the whole is then formed to e desired shape in a die under hydraulic presre.
  • the body so formed isthen heated to a nperature of about 400 C. until the parafiin iding material is completely volatilized without lving any residue.
  • the temperature is regu- ;ed so that the silver nitrate coating has broken wn to silver oxide and the temperature is then adually raised to about 800 0., the oxide coat being thus reduced to metallic silver and the ztallic silver coated particles are sintered tother.
  • the resulting body is highly porous and considerable mechanical strength.
  • Fig. 1 represents an paratus for carrying out the method of the inntion and the formation of a porous metallic dy having zones of difierent degrees of porosity
  • d Fig. 2 represents a finished porous metallic dy having such zones.
  • An ingot of base atal is heat treated as hereinabove described as to form large crystals and then broken down to individual crystals.
  • the crystals are ished, the broken particles screened to form tches graded as to size, and then thoroughly :tted with an aqueous solution of silver nitrate (1 dried.
  • Each batch is then mixed thoroughly th a binding material, such as parafiin dis- .ved in carbon tetrachloride.
  • a batch of very le screenings consisting, for instance, of peanuts that pass through a 300 mesh screen and e retained on a 350 mesh screen, mixed With is binder, is then introduced into the die I to :m a layer as indicated at 4.
  • the plunger 2 then forced down under hydraulic pressure the layer 4 with sufiicient pressure to reduce is material to about two-thirds of its original lume.
  • the plunger is then removed and a :ond batch of screenings 5 consisting, for ample, of particles that pass through a screen 150 mesh and are retained on a 200 mesh reen, is then placed in the die I on top of the rtially pressed layer 4. This material is then 'draulically pressed in about the same degree the bottom layer 4.
  • the plunger 2 is again re- )ved and a third batch 6 consisting of particles ssing a 40 mesh screen and being retained on 60 mesh screen, is then filled into the die I top of the partially compressed layer 5 and bjected to very heavy pressure of the order about 30,000 lbs. to the square inch, thus closely mpacting the entire mass.
  • the block thus formed is then removed from e die I. It is heat treated, as hereinabove deribed, to volatilize out the binder, to reduce the ver nitrate to oxide and ultimately to a metallic ver coating on the particles and to sinter the ated particles into a mechanically strong, corent but porous mass.
  • the resultant body is illustrated in Fig.
  • the first step in the process namely, that of forming the-metal into large crystals, may be accomplished in a variety of ways, and it will be noted that the method used will depend upon the nature of the metal dealt with. If the metal concerned is one having a high melting point, such as tungsten, molybdenum and similar refractory metals, the method given in the example of tungsten will be found most convenient under ordinary circumstances. They Will be formed into an ingot by pressing and sintering and then heat treated to the germinating temperature of the metal.
  • the metal will be melted and cast and then suddenly chilled by quenching it in cold Water.
  • the ingot so formed will be found to have exceedingly large crystals.
  • any method which is effective to produce large crystals in a given particular metal may be used.
  • Metallic bodies formed according to the present invention are characterized by a porous continuity permeating the entire structure and permit the passage of fluids therethrough while obstructing the passage of contaminating solid matter that may be contained in said fluids.
  • Such bodies may be constructed with very small pores intercommunicating with each other so as to retain lubricants within the pores that constantly feed to the surface and function very efliciently as self-lubricating bearings.
  • Metals such as an iron molybdenum manganese alloy or tungsten having the particles coated with lead reduced from lead nitrate in the manner hereinabove described, are especially suitable for use as bearings.
  • Method of making a porous metallic body that comprises making an ingot of metal and treating said metal so as to cause it to form into large crystals; breaking said ingot into its individual crystals, crushing the crystals into crystalline particles; then wetting said particles with a solution of a metallic salt reducible to an oxide under heat, drying said solution on said particles and heat treating said particles until said salt is reduced to an oxide coating on said particles; thenmixing said oxide coated particles With a binding medium, pressing said material in a die to a desired shape and heating at temperatures regulated to volatilize said binding material completely, reduce said oxide coating on said particles to metal and sinter said particles into a strong, coherent, metallic body permeated by intercommunicatin pores.
  • Method of making a porous body of tungsten that comprises making an ingot of tungsten and heat treating said ingot at a temperature of about 2800 C. until said ingot is formed into large crystals; breaking said ingot into its component crystals and crushing said crystals into crystalline particles of irregular sizes and shapes; grading said crystals into batches according to size by screening and mixing the material from said batches in predetermined proportions according to the degree of porosity desired in the finished body; then thoroughly wetting said mixed particles with an aqueous solution of silver nitrate and heating until said nitrate breaks down into a silver oxide coating; then thoroughly mixing said silver oxide coated particles with a solution of paraifin in carbon tetrachloride and shaping the mass so formed in a die under hydraulic pressure; and finally heating said formed mass at temperatures regulated, first, to volatilize said paraffin without leaving a residue, then, to reduce said silver oxide coating to metallic silver and then to sinter said silver coated tungsten particles into a strong, coherent body permeated by intercommunicating
  • Method of making a porous metallic body according to claim 1 in which a plurality of batches of crystalline particles from separate screenings through screens of different mesh after being coated and mixed with binding material are each separately partially pressed in a die in layers one above the other and then further pressed and heat treated to volatilize out said binding material, reduce said coating to metal and finally to sinter the same into a strong, coherent, porous body having zones of different degrees of intercommunicating porosity corresponding to said layers.
  • Method of making a metalli body permeated by intercommunicating pores comprises coating a metal powder consisting of broken crystals with a metallic salt, mixing said coated powder with a volatil-izable binding material, pressing said mixture to a desired shape and heating said body so formed first to a temperature sufiicient to volatilize said binder without leaving any residue, then to a temperature sufllcient to reduce said metal salt coating tometal and then to sinter said coated powder to a strong, coherent, porous body.
  • Method of making a tungsten body permeated by intercommunicating pores comprises coating a tungsten powder consisting of broken tungsten crystals with silver nitrate, mixing said coated tungsten powder with paraffin, pressing said mixture to a desired shape and heating said pressed body at increasing temperatures to volatilize said parafiin without leaving any residue, to reduce said silver nitrate to a metallic silver coating and to sinter said silver coated particles to a strong, coherent, porous body.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Powder Metallurgy (AREA)

Description

March 15, 1949. J. KURTZ METHOD OF MAKING POROUS METALLIC BODIES Filed May 15, 1945 INVENTOR. (/4605 A 0/?7 Z ATTORNEY Patented Mar. 15, 1949 FFECE METHOD OF MAKING POROUS METALLIC BODIES Jacob Kurtz, Tcaneck, N. J., assignor to Callite Tungsten Corporation, Union City, N. J a corporation of Delaware 8 Claims.
The present invention relates to porous metallic bodies and methods of making the same. More particularly, it relates to porous metallic bodies suitable for use as filters and while the method may be used with a wide variety of metals, in its preferred form it is applicable to the formation of porous bodies of refractory metals such as tungsten and molybdenum. It has, however, a special adaptation to alloys such as iron molybdenum manganese alloy, and generally to metals that can be cast and suddenly chilled in a manner to produce a brittle formation of large crystals.
The method may generally be described as, first, forming an ingot or body of other shape having large crystals and a consequent brittleness of structure which permits the breaking up of the body into its component crystals. The individual crystals are of considerable strength and hardness although the body as a whole formed from these crystals is quite brittle. The body is first formed into large crystals either by heating the ingot in the case of the more refractory metals to the germinating temperature, or by casting the ingot and immediately chilling it. The ingot is then broken up into its component crystals and these crystals are again broken down by mechanical means such as ball milling, crushing or hammering.
The crystal fragments so produced vary considerably in size and it is, therefore, desirable to screen the fragments into different batches in which the particles are of approximately equal sizes. This may be done by passing the powdered crystalline material through a series of screens varying from say 40 mesh to about 350 mesh. There may thus be screens of the following sizes which are given by way of example merely: 40 mesh, 60 mesh, 100 mesh, 150 mesh, 20'.) mesh, 250 mesh, 300 mesh, and 350 mesh. By combining the material retained on certain screens with that retained on others, a considerable degree of control of the porosity of the finished body is permitted. Thus, if a given proportion of larger size fragments is mingled with a given proportion of fragments of smaller sizes, a certain degree of porosity of the finished body may be secured, and this porosity may be increased by increasing the proportion of larger size fragments or it may be diminished by increasing the proportion of the smaller size fragments.
When a batch is prepared having a predetermined proportion of large and small size fragments, it is thoroughly wetted with a solution of a soluble salt of a metal such as silver, copper or nickel. The salt used should be one yvhich will break down to the oxide under temperature. For instance, an aqueous solution of silver nitrate may be used and the powdered crystalline metal is thoroughly wetted with this solution and dried so as to form a coating of silver nitrate on the individual particles. It is then heated to a temperature sufficient to break down the nitrate tc the oxide.
A binding material which is decomposable at temperatures below sintering temperature, of the metal with which the powdered base metal is coated and which will volatilize at that temperature without leaving a residue, should be used. Among such binding materials are paraffin dissolved in carbon tetrachloride, salicyclic acid, naphthalene, benzyldichloride, and ammonium chloride, and many others. The coated powdered metal is thoroughly mixed with this binding material and the mass is shaped in a die under hydraulic pressure.
After pressing and shaping in this manner, the mass is then heated in an atmosphere of hydrogen to a temperature suificient to volatilize the binder out of the mass without leaving a carbon residue, and when volatilization is complete the temperature is held sufiiciently high to reduce the oxide coating to a metallic coating. This temperature should be further increased to a point at which the coating metal on the particles will s'inter but it should not be sufficientlyhigh to melt the coating metal to a fluid condition at which it would flow off the particles. There is very little shrinkage of the body under this treatment owing to the fact that at the temperatures used the crystalline fragments show little tendency to coalesce and the voids remaining after the volatilization of the binding material show practically no diminution of size or number. Nowithstanding this lack of shrinkage, the final product has considerable mechanical strength.
The method may be illustrated by describing the formation of such a body from tungsten.
Tungsten powder is first formed under hydraulic pressure in a die to the shape of a bar or ingot. This bar is then sintered and heat treated in a hydrogen atmosphere at the temperature of aspen-1,0 a l fore described, and the particles thus graded cording to size. Batches selected according to e are then thoroughly mixed together in a pretermined manner to produce the desired degree porosity in the finished body and the mass so ."med is thoroughly wetted with an aqueous lution of silver nitrate and then dried. Into e same so formed a solution of parafiin dislved in carbon teterachloride is thoroughly xed and dried, and the whole is then formed to e desired shape in a die under hydraulic presre. The body so formed isthen heated to a nperature of about 400 C. until the parafiin iding material is completely volatilized without lving any residue. The temperature is regu- ;ed so that the silver nitrate coating has broken wn to silver oxide and the temperature is then adually raised to about 800 0., the oxide coat being thus reduced to metallic silver and the ztallic silver coated particles are sintered tother. The resulting body is highly porous and considerable mechanical strength.
The invention will be more clearly understood )m the drawings in which Fig. 1 represents an paratus for carrying out the method of the inntion and the formation of a porous metallic dy having zones of difierent degrees of porosity, d Fig. 2 represents a finished porous metallic dy having such zones.
Referring now to Fig. 1, a mold or die I having erein a movable plunger 2 and a stationary inger or stop 3, is provided. An ingot of base atal is heat treated as hereinabove described as to form large crystals and then broken down to individual crystals. The crystals are ished, the broken particles screened to form tches graded as to size, and then thoroughly :tted with an aqueous solution of silver nitrate (1 dried. Each batch is then mixed thoroughly th a binding material, such as parafiin dis- .ved in carbon tetrachloride. A batch of very le screenings consisting, for instance, of parles that pass through a 300 mesh screen and e retained on a 350 mesh screen, mixed With is binder, is then introduced into the die I to :m a layer as indicated at 4. The plunger 2 then forced down under hydraulic pressure the layer 4 with sufiicient pressure to reduce is material to about two-thirds of its original lume. The plunger is then removed and a :ond batch of screenings 5 consisting, for ample, of particles that pass through a screen 150 mesh and are retained on a 200 mesh reen, is then placed in the die I on top of the rtially pressed layer 4. This material is then 'draulically pressed in about the same degree the bottom layer 4. The plunger 2 is again re- )ved and a third batch 6 consisting of particles ssing a 40 mesh screen and being retained on 60 mesh screen, is then filled into the die I top of the partially compressed layer 5 and bjected to very heavy pressure of the order about 30,000 lbs. to the square inch, thus closely mpacting the entire mass. The block thus formed is then removed from e die I. It is heat treated, as hereinabove deribed, to volatilize out the binder, to reduce the ver nitrate to oxide and ultimately to a metallic ver coating on the particles and to sinter the ated particles into a mechanically strong, corent but porous mass. The resultant body is illustrated in Fig. 2 in 11611 it Will be seen that the original layers 4, 5 d 6 are still roughly preserved but that where e layers contact each other, part of each layer is forced into the other by reason of the heavy pressure ultimately applied. Marginal layers of this sort are indicated in Fig. 2 at I and 8. It will thus be obvious that in this manner the porosity of the finished body may be regulated from a high porosity at 6 through zones of decreasing porosity to 4.
The first step in the process, namely, that of forming the-metal into large crystals, may be accomplished in a variety of ways, and it will be noted that the method used will depend upon the nature of the metal dealt with. If the metal concerned is one having a high melting point, such as tungsten, molybdenum and similar refractory metals, the method given in the example of tungsten will be found most convenient under ordinary circumstances. They Will be formed into an ingot by pressing and sintering and then heat treated to the germinating temperature of the metal. On the other hand, with lower melting point metals and many alloys, such as the alloy of iron, molybdenum and manganese hereinabove suggested, the metal will be melted and cast and then suddenly chilled by quenching it in cold Water. The ingot so formed will be found to have exceedingly large crystals. In fact, any method which is effective to produce large crystals in a given particular metal may be used.
Metallic bodies formed according to the present invention are characterized by a porous continuity permeating the entire structure and permit the passage of fluids therethrough while obstructing the passage of contaminating solid matter that may be contained in said fluids. Such bodies may be constructed with very small pores intercommunicating with each other so as to retain lubricants within the pores that constantly feed to the surface and function very efliciently as self-lubricating bearings. Metals such as an iron molybdenum manganese alloy or tungsten having the particles coated with lead reduced from lead nitrate in the manner hereinabove described, are especially suitable for use as bearings.
Having thus described my invention, what I claim is:
1. Method of making a porous metallic body that comprises making an ingot of metal and treating said metal so as to cause it to form into large crystals; breaking said ingot into its individual crystals, crushing the crystals into crystalline particles; then wetting said particles with a solution of a metallic salt reducible to an oxide under heat, drying said solution on said particles and heat treating said particles until said salt is reduced to an oxide coating on said particles; thenmixing said oxide coated particles With a binding medium, pressing said material in a die to a desired shape and heating at temperatures regulated to volatilize said binding material completely, reduce said oxide coating on said particles to metal and sinter said particles into a strong, coherent, metallic body permeated by intercommunicatin pores.
2. Method of making a porous body of tungsten that comprises making an ingot of tungsten and heat treating said ingot at a temperature of about 2800 C. until said ingot is formed into large crystals; breaking said ingot into its component crystals and crushing said crystals into crystalline particles of irregular sizes and shapes; grading said crystals into batches according to size by screening and mixing the material from said batches in predetermined proportions according to the degree of porosity desired in the finished body; then thoroughly wetting said mixed particles with an aqueous solution of silver nitrate and heating until said nitrate breaks down into a silver oxide coating; then thoroughly mixing said silver oxide coated particles with a solution of paraifin in carbon tetrachloride and shaping the mass so formed in a die under hydraulic pressure; and finally heating said formed mass at temperatures regulated, first, to volatilize said paraffin without leaving a residue, then, to reduce said silver oxide coating to metallic silver and then to sinter said silver coated tungsten particles into a strong, coherent body permeated by intercommunicating pores.
3. Method of making a porous metallic body according to claim 1, in which a plurality of batches of crystalline particles from separate screenings through screens of different mesh after being coated and mixed with binding material are each separately partially pressed in a die in layers one above the other and then further pressed and heat treated to volatilize out said binding material, reduce said coating to metal and finally to sinter the same into a strong, coherent, porous body having zones of different degrees of intercommunicating porosity corresponding to said layers.
4. Method of making a porous metallic body according to claim 1 in which an ingot is made of a refractory metal and is formed into large crystals by heating at the temperature of rapid germination until said ingot is formed into large crystals.
5. Method of making a porous metallic body according to claim 1 in which an ingot is formed of a metal that is cast and suddenly chilled, thereby forming said ingot into large crystals.
6. The method of forming a porous metallic body having zones of different degrees of porosity that consists in forming a metallic body and heat treating it to form large crystals therein; then breaking said body down to its component crystals and crushing said crystals; then screening said crushed crystals to separate the crushed particles into batches of diiferent sizes; then wetting said batches with metallic salts and heating to reduce said salts to oxides, thereby forming an oxide coating on the crystalline fragments; then mixing batches of difierent sized particles with a binding material and filling said batches into a die in layers of difierent sized particles and pressing said layers under hydraulic pressure; then heating to volatilize said binding material without leaving any residue and to reduce the oxide coating on said particles to metal; and finally further heating so as to sinter said coated metal powders into a body comprising layers of diifereni degrees of intercommunicating porosity according to the particle sizes of the crystalline fragments composing each layer.
7. Method of making a metalli body permeated by intercommunicating pores that comprises coating a metal powder consisting of broken crystals with a metallic salt, mixing said coated powder with a volatil-izable binding material, pressing said mixture to a desired shape and heating said body so formed first to a temperature sufiicient to volatilize said binder without leaving any residue, then to a temperature sufllcient to reduce said metal salt coating tometal and then to sinter said coated powder to a strong, coherent, porous body.
8. Method of making a tungsten body permeated by intercommunicating pores that comprises coating a tungsten powder consisting of broken tungsten crystals with silver nitrate, mixing said coated tungsten powder with paraffin, pressing said mixture to a desired shape and heating said pressed body at increasing temperatures to volatilize said parafiin without leaving any residue, to reduce said silver nitrate to a metallic silver coating and to sinter said silver coated particles to a strong, coherent, porous body.
JACOB KURTZ.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 912,246 Kuzel Feb. 9, 1909 1,205,080 Baumann Nov. 14, 1916 1,226,470 Coolidge May 15, 1917 1,566,793 Gero Dec. 22, 1925 1,739,068 Harris Dec. 10, 1929 1,823,869 Baur Sept. 15, 1931 2,110,967 Andrews Mar. 15, 1938 2,133,292 Gordon Oct, 18, 1938 2,199,620 Davis May, 7, 1940 2,206,616 Devereux July 2, 1940 2,267,918 I-Iildabolt Dec. 30, 1941 2,298,908 Wentworth Oct. 13, 1942 2,319,240 Larsen May 18, 1943 2,332,737 Marvin et al Oct. 26, 1943 2,370,242 Hensel Feb. 27, 1945 FOREIGN PATENTS Number Country Date 555,983 Great Britain Sept. 15. 1943
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Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2666696A (en) * 1950-01-31 1954-01-19 Rca Corp Method of treating metal powders
US2702021A (en) * 1948-09-11 1955-02-15 Parker Pen Co Fountain pen
US2712299A (en) * 1948-08-24 1955-07-05 Parker Pen Co Fountain pen
US2721378A (en) * 1951-06-11 1955-10-25 Birmingham Small Arms Co Ltd Process for manufacture of porous structure
US2728134A (en) * 1950-03-20 1955-12-27 Allied Prod Corp Process of making perforated composite oil well bearings
US2751293A (en) * 1951-07-31 1956-06-19 Allied Prod Corp Process of making perforated powdered metal article
US2776887A (en) * 1952-08-22 1957-01-08 Westinghouse Electric Corp Preparation of molybdenum
US2935396A (en) * 1957-03-07 1960-05-03 Dow Chemical Co Cellularized light metal
US2973842A (en) * 1956-07-06 1961-03-07 Gen Motors Corp Friction element
US3087233A (en) * 1960-11-16 1963-04-30 Fram Corp Pervious metal fiber material and method of making the same
DE1149972B (en) * 1956-07-25 1963-06-06 Commissariat Energie Atomique Method of making a permeable membrane
US3145102A (en) * 1961-02-24 1964-08-18 Herman C Simonich Method of and apparatus for making sintered powdered metal parts
US3350200A (en) * 1964-06-27 1967-10-31 Bosch Gmbh Robert Method of making a sintered fuel cell electrode structure
US3360348A (en) * 1964-05-15 1967-12-26 Siemens Ag Composite structure of inter-bonded metals for heavy-duty electrical switch contacts
US3364019A (en) * 1965-01-21 1968-01-16 Leesona Corp Method of making fuel cell electrodes
DE1261482B (en) * 1961-04-08 1968-02-22 Sintermetallwerke Krebsoege G Filter cartridge made of sintered materials
US3382067A (en) * 1965-07-20 1968-05-07 Bosch Gmbh Robert Preparation of double-layer electrodes
US3414394A (en) * 1965-06-21 1968-12-03 Owens Illinois Inc Sintered glass article and method of making
US3421864A (en) * 1965-06-07 1969-01-14 Nasa Multilayer porous ionizer
US3441933A (en) * 1967-04-03 1969-04-29 Raytheon Co Radio frequency absorber
US3471287A (en) * 1966-06-29 1969-10-07 Leesona Corp Process of making multiporous fuel cell electrodes
US3873392A (en) * 1971-06-14 1975-03-25 Ethyl Corp Pressure contouring and bonding of metal foams
US4100664A (en) * 1975-01-17 1978-07-18 Caterpillar Tractor Co. Apex seal for rotary engines
US4381998A (en) * 1981-08-27 1983-05-03 U.S. Environmental Products, Inc. Rigid filter plate and process for manufacture of the same
US4452698A (en) * 1981-08-27 1984-06-05 U.S. Environmental Products, Inc. Rigid filter plate and process for manufacture of the same
US4481114A (en) * 1980-10-30 1984-11-06 International Sludge Reduction Company Sludge dewatering system
US4632764A (en) * 1979-11-30 1986-12-30 International Sludge Reduction Company Sludge dewatering process using multiple layer plate
US4724078A (en) * 1983-10-25 1988-02-09 Ceraver Porous material and tubular filter made of said material
US4822312A (en) * 1983-12-05 1989-04-18 Gte Products Corporation Electrode for high intensity discharge lamps
US4830822A (en) * 1985-08-26 1989-05-16 Gte Products Corporation Variable density article and method for producing same
US4957819A (en) * 1988-06-10 1990-09-18 Haruyuki Kawahara Frameless and coreless porous endosseous implant
EP0446673A1 (en) * 1990-03-14 1991-09-18 Asea Brown Boveri Ag Process for preparing a sintered article having a compact outer layer and a smooth surface
US5820721A (en) * 1991-07-17 1998-10-13 Beane; Alan F. Manufacturing particles and articles having engineered properties
US5943546A (en) * 1992-09-24 1999-08-24 Toto Ltd. Gradient function material
US20080112833A1 (en) * 2003-01-08 2008-05-15 Inco Limited Component produced or processed by powder metallurgy, and process for producing it

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US912246A (en) * 1907-03-26 1909-02-09 Hans Kuzel Manufacturing alloys.
US1205080A (en) * 1913-03-08 1916-11-14 Wolfram Lampen Ag Process of manufacturing filaments for incandescent electric lamps.
US1226470A (en) * 1915-02-20 1917-05-15 Gen Electric Refractory-metal tube.
US1566793A (en) * 1923-06-14 1925-12-22 Westinghouse Lamp Co Method of alloying rare metals and articles made therefrom
US1739068A (en) * 1929-01-31 1929-12-10 Bell Telephone Labor Inc Method of producing materials in finely-divided form
US1823869A (en) * 1926-09-11 1931-09-15 Baur Walter Coating of bodies with metal
US2110967A (en) * 1935-01-15 1938-03-15 Western Electric Co Magnetic materials and methods of making such materials
US2133292A (en) * 1934-08-16 1938-10-18 Gordon Frederick Felix Compound metal bodies
US2199620A (en) * 1937-11-10 1940-05-07 Gen Motors Corp Method of sizing and riveting porous metal articles
US2206616A (en) * 1938-09-17 1940-07-02 Andrew R Devereux Osmium composition and method of making same
US2267918A (en) * 1940-03-27 1941-12-30 Gen Motors Corp Porous article and method of making same
US2298908A (en) * 1940-12-31 1942-10-13 Rca Corp Powdered metal
US2319240A (en) * 1940-03-19 1943-05-18 Mallory & Co Inc P R Electric contact and the like
GB555983A (en) * 1941-03-22 1943-09-15 Sandvikens Jernverks Ab Process of manufacturing sintered moulded bodies of metals and alloys
US2332737A (en) * 1940-07-23 1943-10-26 Gen Motors Corp Composite metal article
US2370242A (en) * 1943-01-15 1945-02-27 Mallory & Co Inc P R Refractory metal composition

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US912246A (en) * 1907-03-26 1909-02-09 Hans Kuzel Manufacturing alloys.
US1205080A (en) * 1913-03-08 1916-11-14 Wolfram Lampen Ag Process of manufacturing filaments for incandescent electric lamps.
US1226470A (en) * 1915-02-20 1917-05-15 Gen Electric Refractory-metal tube.
US1566793A (en) * 1923-06-14 1925-12-22 Westinghouse Lamp Co Method of alloying rare metals and articles made therefrom
US1823869A (en) * 1926-09-11 1931-09-15 Baur Walter Coating of bodies with metal
US1739068A (en) * 1929-01-31 1929-12-10 Bell Telephone Labor Inc Method of producing materials in finely-divided form
US2133292A (en) * 1934-08-16 1938-10-18 Gordon Frederick Felix Compound metal bodies
US2110967A (en) * 1935-01-15 1938-03-15 Western Electric Co Magnetic materials and methods of making such materials
US2199620A (en) * 1937-11-10 1940-05-07 Gen Motors Corp Method of sizing and riveting porous metal articles
US2206616A (en) * 1938-09-17 1940-07-02 Andrew R Devereux Osmium composition and method of making same
US2319240A (en) * 1940-03-19 1943-05-18 Mallory & Co Inc P R Electric contact and the like
US2267918A (en) * 1940-03-27 1941-12-30 Gen Motors Corp Porous article and method of making same
US2332737A (en) * 1940-07-23 1943-10-26 Gen Motors Corp Composite metal article
US2298908A (en) * 1940-12-31 1942-10-13 Rca Corp Powdered metal
GB555983A (en) * 1941-03-22 1943-09-15 Sandvikens Jernverks Ab Process of manufacturing sintered moulded bodies of metals and alloys
US2370242A (en) * 1943-01-15 1945-02-27 Mallory & Co Inc P R Refractory metal composition

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2712299A (en) * 1948-08-24 1955-07-05 Parker Pen Co Fountain pen
US2702021A (en) * 1948-09-11 1955-02-15 Parker Pen Co Fountain pen
US2666696A (en) * 1950-01-31 1954-01-19 Rca Corp Method of treating metal powders
US2728134A (en) * 1950-03-20 1955-12-27 Allied Prod Corp Process of making perforated composite oil well bearings
US2721378A (en) * 1951-06-11 1955-10-25 Birmingham Small Arms Co Ltd Process for manufacture of porous structure
US2751293A (en) * 1951-07-31 1956-06-19 Allied Prod Corp Process of making perforated powdered metal article
US2776887A (en) * 1952-08-22 1957-01-08 Westinghouse Electric Corp Preparation of molybdenum
US2973842A (en) * 1956-07-06 1961-03-07 Gen Motors Corp Friction element
DE1149972B (en) * 1956-07-25 1963-06-06 Commissariat Energie Atomique Method of making a permeable membrane
US2935396A (en) * 1957-03-07 1960-05-03 Dow Chemical Co Cellularized light metal
US3087233A (en) * 1960-11-16 1963-04-30 Fram Corp Pervious metal fiber material and method of making the same
US3145102A (en) * 1961-02-24 1964-08-18 Herman C Simonich Method of and apparatus for making sintered powdered metal parts
DE1261482B (en) * 1961-04-08 1968-02-22 Sintermetallwerke Krebsoege G Filter cartridge made of sintered materials
US3360348A (en) * 1964-05-15 1967-12-26 Siemens Ag Composite structure of inter-bonded metals for heavy-duty electrical switch contacts
US3350200A (en) * 1964-06-27 1967-10-31 Bosch Gmbh Robert Method of making a sintered fuel cell electrode structure
US3364019A (en) * 1965-01-21 1968-01-16 Leesona Corp Method of making fuel cell electrodes
US3421864A (en) * 1965-06-07 1969-01-14 Nasa Multilayer porous ionizer
US3414394A (en) * 1965-06-21 1968-12-03 Owens Illinois Inc Sintered glass article and method of making
US3382067A (en) * 1965-07-20 1968-05-07 Bosch Gmbh Robert Preparation of double-layer electrodes
US3471287A (en) * 1966-06-29 1969-10-07 Leesona Corp Process of making multiporous fuel cell electrodes
US3441933A (en) * 1967-04-03 1969-04-29 Raytheon Co Radio frequency absorber
US3873392A (en) * 1971-06-14 1975-03-25 Ethyl Corp Pressure contouring and bonding of metal foams
US4100664A (en) * 1975-01-17 1978-07-18 Caterpillar Tractor Co. Apex seal for rotary engines
US4632764A (en) * 1979-11-30 1986-12-30 International Sludge Reduction Company Sludge dewatering process using multiple layer plate
US4481114A (en) * 1980-10-30 1984-11-06 International Sludge Reduction Company Sludge dewatering system
US4381998A (en) * 1981-08-27 1983-05-03 U.S. Environmental Products, Inc. Rigid filter plate and process for manufacture of the same
US4452698A (en) * 1981-08-27 1984-06-05 U.S. Environmental Products, Inc. Rigid filter plate and process for manufacture of the same
US4724078A (en) * 1983-10-25 1988-02-09 Ceraver Porous material and tubular filter made of said material
US4822312A (en) * 1983-12-05 1989-04-18 Gte Products Corporation Electrode for high intensity discharge lamps
US4830822A (en) * 1985-08-26 1989-05-16 Gte Products Corporation Variable density article and method for producing same
US4957819A (en) * 1988-06-10 1990-09-18 Haruyuki Kawahara Frameless and coreless porous endosseous implant
EP0446673A1 (en) * 1990-03-14 1991-09-18 Asea Brown Boveri Ag Process for preparing a sintered article having a compact outer layer and a smooth surface
US5820721A (en) * 1991-07-17 1998-10-13 Beane; Alan F. Manufacturing particles and articles having engineered properties
US5943546A (en) * 1992-09-24 1999-08-24 Toto Ltd. Gradient function material
US5972067A (en) * 1992-09-24 1999-10-26 Toto Ltd. Gradient function material seal cap for discharge lamp bulb
US20080112833A1 (en) * 2003-01-08 2008-05-15 Inco Limited Component produced or processed by powder metallurgy, and process for producing it
US8802004B2 (en) * 2003-01-08 2014-08-12 Alantum Corporation Component produced or processed by powder metallurgy, and process for producing it

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