US2192741A - Method of making a sintered alloy - Google Patents

Method of making a sintered alloy Download PDF

Info

Publication number
US2192741A
US2192741A US164354A US16435437A US2192741A US 2192741 A US2192741 A US 2192741A US 164354 A US164354 A US 164354A US 16435437 A US16435437 A US 16435437A US 2192741 A US2192741 A US 2192741A
Authority
US
United States
Prior art keywords
alloy
iron
aluminum
sintered
cooling
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US164354A
Inventor
Goodwin H Howe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Priority to US164354A priority Critical patent/US2192741A/en
Priority to US182087A priority patent/US2142846A/en
Priority to US183146A priority patent/US2197642A/en
Priority to US196691A priority patent/US2192743A/en
Application granted granted Critical
Publication of US2192741A publication Critical patent/US2192741A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • 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
    • 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
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/4902Electromagnet, transformer or inductor
    • Y10T29/49075Electromagnet, transformer or inductor including permanent magnet or core
    • Y10T29/49076From comminuted material

Definitions

  • the present invention relates to sintered alloys containing a readily oxidizable element and more particularly to sintered permanent magnets of the type disclosed in Mishima Patents 2,027,994 to 2,028,000 inclusive, and in Ruder Patents 1,947,274 and 1,968,569 and to a method of making the same.
  • Permanent magnet alloys of the type disclosed in the Mishima and Ruder patents contain iron, nickel and aluminum as the basic or essential ingredients. However, it is well known to include other elements such as cobalt, copper, silicon, titanium, chromium, molybdenum, tungsten and manganese in the alloys if desired and as indicated in the above patents.
  • Preferred permanent magnet compositions are those containing about 6 to aluminum, 17 to 35% nickel with the remainder iron; or 6 to 15% aluminum, l2 to 35% nickel, an appreciable quantity up to 18% cobalt with the remainder iron; or an alloy disclosed in Ruder application Serial No. 96,854 filed August 19, 1936, which may consist of about 14 to 25% nickel, about 8 to 13% aluminum, about 2 to 18% cobalt, about 2 to 16% copper with the remainder iron.
  • One of the objects of the present invention is to provide a hard, dense, sintered alloy containing a readily oxidizable ingredient such as aluminum. It is also an object of the -invention to provide a continuous method for producing sintered alloys containing aluminum as one of the principal ingredients. It is a further object of ythe invention to provide permanent magnets of the composition disclosed in the above noted Ruder and Mishima patents which will require a minimum of finish grinding, which shall be fine grained, uniform in character and have a high tensile and transverse strength as well as highly desirable permanent magnet characteristics. Other objects will appear hereinafter.
  • Fig. 1 is a view in elevation of a hydrogen furnace which may be employed in carrying my invention into effect
  • Fig. 2 is a longitudinal sectional view, broken away and on an enlarged scale, of the apparatus disclosed in Fig. 1
  • Fig. 3 is anend view of the apparatus shown in Fig. 2
  • Fig. 4 is a perspective view of a boat employed in the operation of the furnace and adapted to hold the material to be sintered.
  • the process which I employ may or may not be continuous. In both processes, however, oxidation of the aluminum content of the alloy may be avoided by the use of a foundation alloy.
  • the foundation alloy preferably is a very brittle iron-aluminum alloy which consists of about 50% aluminum and 50% iron, and contains all the aluminum present in the final alloy.l
  • the necessary quantity of iron which may comprise several pieces of ordinary melting stock, is heated in a high frequency induction or other suitable furnace to an elevated temperature, for example, a temperature in the neighborhood of 1000 C. This temperature is several hundred degrees below the melting point of iron but is suiiiciently high to permit alloyage of aluminum with iron.
  • Aluminum which likewise may comprise several pieces of ordinary melting stock, is added to the iron to form an alloy consisting substantially of 50% iron and 50% aluminum.
  • the molten alloy is poured into a graphite or other suitable mold to solidify.
  • the alloy thus produced is very brittle and may be crushed easily, it also remains stable; that is, it does not disintegrate physically when exposed to atmospheric conditions.
  • the foundation alloy is crushed to the desired extent and added to the other nely divided ingredients present in the magnetic alloy, for example, iron and nickel, or iron, nickel and cobalt, etc., to provide the desired alloy composition.
  • the finely divided materials are mixed, usually in a ball mill, for about iive hours and then pressed into a desired shape in a steel mold. The pressed mixture may then be placed in a closed tube having a small outletopeningat one end.
  • the tube Vis supplied with pure dry hydrogen or other reducing gas, positioned in ahydrcgen furnace, and sintered at a temperature above 1000 and preferably at about 1400" C.
  • the time required to complete the sintering action may vary from about one-half to iive hours depending upon the load and size of the pieces to be sintered.
  • the material After the material has been sintered into a hard, dense mass, it preferably is normalized by heating for about one hour at a temperature above 1000". C. but not materially higher than 1400" C. and preferably at a temperature of about 1050 to about 1100 C. No advantage is obtained by employing a normalizing temperature materially higher than about 1l00 C. Any red furnace may be employed in the normalizing operation since the sintered alloy does not tend to become appreciably oxidized.
  • the alloy may be cooled from the normalizing temperature in still air although, under certain circumstances, the cooling may be accelerated by means of an air blast or slowed down by cooling a plurality of parts in contact with one another. Also parts of small cross sections that would cool too fast in still air can be retarded to a proper rate of cooling by introduction into an air furnace running at about 500 to 600 C.
  • the cross section of the magnetic material determines to some extent the cooling rate to be employed.
  • a bar consisting of iron, nickel, aluminum and cobalt about one-cuarter inch square preferably should be cooled in still air to obtain the best magnetic qualities, while bars of the same composition and about one-half inch souare should be cooled in moving air. If bars of the same composition are about one inch square and over they should be cooled in an air blast or in an air blast moistened with a cooling medium.
  • the permanent magnet properties of the alloy vary with the rate of cooling from the normalizing temperature. For example, an iron, nickel, aluminum alloy one-quarter inch by onehalf inch in cross section cooled in an air-blast at the rate of about 600 C. per minute has a residual of about 6900 and a coercive force of about 445.
  • the same cooling rate applied to an iron, nickel, aluminum, cobalt alloy of the same cross section gives a residual of 8100 but a low coercive force of about 315.
  • the same iron, nickel, aluminum. cobalt alloy Vof the same dimensions when cooled at a slower rate, as in still air, has a residual of 7800 and a coercive force of about 360.
  • the alloy may be cooled at the desired rate directly after the sintering operation and the normalizing treatment omitted without impairment of the magnetic properties of the alloy.
  • Such a process however is not as satisfactory economically as the process employing the normalizing step.
  • the container with the sintered material therein may be removed from the furnace and the sintered material taken out of the container while the container is at an elevated temperature. Under such circumstances the interior of the container will become oxidized and the oxide coating must be removed before the tube is again used for the sintering operation. If the container and load therein are removed from the furnace and allowed to cool to room temperature the rate of cooling may be too slow due to the bulk of the container and the load therein.
  • the alloy after sintering or normalizing, is cooled in air at the proper rate for that alloy the optimum atomic arrangement for best permanent magnet properties is obtained so that reheating of the material at temperatures between about 500 C. and 700 C.'at the end of cooling period to eifect ageing or precipitation may be omitted if desired.
  • cooling in air after the sintering or normalizing treatment my invention is not limited to cooling in any particular atmosphere. If desired, the cooling action may be carried out in substantially any gaseous medium without adversely affecting the magnetic or physical properties of the material, for example in the cooling chamber of the ordinary hydrogen furnace. Where I employ the expression cooling in air in the specification or claims, I have reference to a type of cooling rather than to cooling in a certain gaseous medium.
  • the sintered alloy containing iron, nickel, and aluminum as basic ingredients may be machined. However, in general, it will be found easier to carry out any desired machining operation either on the material as pressed and before sintering, or on the pressed and partly sintered material. In the latter case the material which has been mixed and pressed, as heretofore pointed out, is heated at a temperature oi about 600 C. for about one hour in a hydrogen or other suitable reducing atmosphere to effect partial sintering. It is then cooled rapidly, preferably in the cooling chamber of the furnace, to prevent oxidation of the iron, nickel and aluminum.
  • I may employ a modified form of hydrogen furnace i.
  • the furnace comprises the usual heating chamber 2, supplied With hydrogen gas through the pipe
  • An elongated rectangular shaped steel tube l which extends through and beyond each .end of the heating chamber of furnace i, comprises a heating or sintering chamber 5 coextensive with the heating chamber 2, and a cooling chamber 6 which forms an extension of the sintering chamber 5.
  • the inlet and outlet ends of tube S are provided with doors or closure members l and 8 respectively.
  • y Outlet door is provided with an opening il which in the present case is about .040" in diameter, while the inlet door ll is provided with .an opening l about .052" in diameter.
  • Slotted pipes i l and l2 positioned beneath these doors, supply a curtain of hydrogen over the ends of the tube l and prevent access of air, particularly by convection, to the interior of the tube when either door is opened.
  • the portion of the .tube El comprising the cooling chamber 6 is cooled by a water jacket i3, having an inlet pipe l0 and an outlet pipe l5 for the circulation of a cooling medium therethrough.
  • the tube i is heated to a temperature above 1000 C. and preferably at about 1400 l C. by means of the usual heater coil it.
  • Hydrogen which preferably has been purified and dried to remove moisture therefrom, lis supplied to the tube at a point between the heating and cooling zones through a pipe il.
  • Ordinary line hydrogen may be supplied to the heating zone 2 of the furnace I through pipe 3. This hydrogen is burned as it emerges from the opening i8, while the hydrogen intube d is burned as it emerges from openings 9 and I0.
  • 'I'he pieces of material I9 to be sintered are positioned on metal boats 20 which are pushed slowly through tube 4 by means of a rod 2l operated by a driving device 22.
  • the purified hydrogen is further purified by the removalof substantially all traces of oxygen therefrom. No reaction to form water takes place, however, as the surface of the sintered material, in this case, permanent magnet material containing as essential ingredients, iron,
  • nickel, and aluminum is practically inert to re- In a 4 furnace of the type disclosed and havingoutlets as designated, the magnetic properties of sintered alloy are progressively improved as the hydrogen ow is increased from about 4 to 10 cubic feet per hour.
  • powdered materials aire employed in fabricating the alloys, some degree of oxidation of the powdered materials occurs during mixing and pressing.
  • the hydrogen iiow is in the proper direction to maintain an extremely high degree of purity at the inlet point of tube l*l where the demand is most critical.
  • the time required for a boat 20 to pass through the heating zone in the tube i usually varies from about one-half to two hours depending upon the size of the pieces to be sintered.
  • the temperature of the hot zone grades off from about 1400" C. at the center to about 1050 C. to 1150 C. at the end adjoining the cooling chamber.
  • the cooling period usually varies from about 10 to about 30 minutes according to the composition, size of pieces i9, and magnetic properties desired.
  • the cooling rate may be co-ntrolled by varying the rate of ow of the cooling medium in water jacket I3.
  • 'I'he atmospheric conditions in the hot section of the sintering section of tube i are ideal for causing sticking of the boats to the tube d owing to the reducing action of the hydrogen and the high temperature employed.
  • a. composite type of boat 20 may be employed.
  • iron powder is mixed with a smaller quantity of aluminum oxide powder, for example about 75% iron and about 25% aluminum oxide and spread into a relatively thin even layer having the surface dimensions desired for the finished part.
  • a second and thicker layer of powdered iron is then superimposed on the first mentioned layer and the two layers pressed together in a mold and then sintered for about two hours at about 1450 C.
  • Two or more metal pieces thus fabricated may be readily welded together, owing to the presence of the iron layer, to provide boats of any desired width. End pieces 23 having the oxide-iron mixture on the outside are welded to the base portion of the boat. A boat may be pressed entirely of the 25 A1203- 75 Fe mixture but such material cannot be welded and unless a. large enough mold is available to press a complete boat it is necessary to use pieces of composite construction having weldable material on one side. Another advantage in using a composite boat is that any deformation of the boat due to alternate heating and cooling may be removed by cold pressing without danger of breakage or oxidation.
  • the product obtained by mixing and pressing powdered iron, nickel, and aluminum, or other similar mixtures containing aluminum, and thereafter sintering in a hydrogen atmosphere is substantially as good magnetically and in appearance as that obtained when a foundation alloy of iron and aluminum is employed in fabricating the alloy.
  • the finished sintered alloy has permanent magnet properties equal to those of an alloy of the same composition made by casting and heat treating.
  • the sintered alloy is fine grained and has tensile and transverse strengths which are respectively ten and ve times greater than the tensile and transverse strengths of cast alloys cf the same composition.
  • Thelsintered alloy requires a minimum of grinding which may be carried out without any danger of cracking the alloy.
  • solid or hollow inserts may be made in the pressed material. Under such circumstances however the holes drilled in the pressed material should be slightly larger than the inserts to thereby prevent cracking or distortion when the material is sintered.
  • the sintered product made by the continuous process has the additional advantage of having a very bright finish.
  • the mixed ingredients In fabricating the sintered magnetic alloy, the mixed ingredients usually are subjected to a pressure of about 10 to 30 tons per square inch. Material which has been subjected to such pressure shrinks about 6 to 14% during the sintering operation, the greater shrinkage occurring ,With
  • Sintered magnets have an additional advantage in economy of material due to the fact that there is no waste material such as the gates and risers which are formed during the process of manufacturing cast materials.
  • the alloy material preferably is shaped by pressure in a steel mold, it also may be formed in some cases by extruding the mixed ingredients with a binder material of which starch is an example. The extruded material may then be heat treated as hereinbefore set forth.v
  • foundation alloy consisting of about 50% iron and about 50% aluminum
  • other percentages of iron and aluminum may be employed in the fabrication of the foundation alloy.
  • the foundation alloy may be formed by alloying the aluminum with either cobalt or nickel, or with iron and cobalt in Various percentages.
  • the alloy consisting of 50% iron and 50 aluminum is, in general, the most satis factory owing to the low temperature at which it can be manufactured and the ease with which it may be crushed.
  • oxidation resistant alloys containing iron, aluminum and chromium may be formed either by pressing a mixture of the powdered elements and then sintering itin a hydrogen furnace as hereinbefore set forth, or by first making a base or foundation alloy of iron and aluminum, as also hereinbefore set forth, and then crushing the foundation alloy, mixing it with the chromium and the remainder of the iron, pressing the mixture into a desired shape and then sintering the shaped material.
  • Such alloys when made by melting and casting are very brittle but when fabricated in the manner indicated above they are ductile and when employed as resistance wire have a far longer life at temperatures of say 1200 C. than wire containing the same ingredients and made from cast material.
  • a magnetic alloy consisting substantially of iron, aluminum and metal from a group consisting of nickel and coamarsi balt which comprises alloying the aluminum with a portion of the iron to provide a foundation alloy consisting of about 50% aluminum and 50% iron, pulverizing said alloy and mixing it with the remaining ingredients present in the final alloy, pressing and sintering the mixed powdered materials, normalizing the sintered product at a temperature of about 1050 C. and air cooling from the normalizing temperature.
  • the method of making a magnetic alloy containing aluminum and iron which comprises forming a casting containing about 50% aluminum and 50% iron, pulverizing said casting, mixing said pulverized material with the other ingredients of said alloy, pressing the mixture into a desired shape, sintering the pressed material at a temperature above 1000 C. and air cooling the sintered material.
  • the method of making a sintered alloy which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving said pressed material through the heating zone of a furnace to thereby sinter said alloy and suddenly removing the sintered alloy from said heating zone to a controlled cooling zone the rate of cooling employed in said cooling zone eecting precipitation in said alloy.
  • the method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the mixed powdered ingredients comprising the alloy into a desired shape, continuously moving a series of boats containing said pressed material through a hydrogen furnace heated to a temperature of about 1400 C. and in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy.
  • the method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the mixed powdered ingredients comprising the alloy into a desired shape, moving the pressed material through the heating zone of a hydrogen furnace in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy, and suddenly moving the sintered material from the heating zone into the cooling zone of said furnace the rate of cooling employed in said cooling zone eilecting precipitation in said alloy.
  • the method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the powdered ingredients comprising the alloy into a desired shape, moving the pressed material through the heating zone of a hydrogen furnace in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy, and cooling the alloy in a current of hydrogen having a direction of flow which is opposite to that of the hydrogen in said heating zone.
  • the method of making an alloy containin iron, nickel and aluminum as basic ingredients which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving the pressed material through the heating zone of a furnace while said material is in contact with a puried reducing atmosphere to thereby sinter the alloy, suddenly removing the alloy from said heating zone to a cooling zone in said furnace and controlling the temperature of said cooling zone to eiect a condition of precipitation in said alloy.
  • the method of making an alloy containing iron, nickel and aluminum as basic ingredients which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving the pressed material through a container which extends through the heating zone of a furnace whereby said pressed material may be sintered, surrounding the portion of said container Within said heating zone with a reducing atmosphere. supplying a purified reducing atmospherev to said container, suddenly removing the sintered material from said heating zone to a cooling zone in said container and controlling the temperature of said cooling zone to effect a condition of precipitation in said sintered material.

Description

Mwah 5, M4@ G. H. How
METHOD OF MAKING A SINTERED ALLOY Original Filed Sept. 1'7, 1937' inventor: Goodwin H. Howe,
or precipitation.
Patented Mar. 5, 1940 G A SINTERED ALLOY Good H. Howe, Scotia, N. Y., assignor to General Electric Company, a corporation of New York Application September 17, 1937, Serial No. 164,354- Renewed October 11, 1939 This application is a continuation in part of my prior application Serial No. 758,990, led December 24, 1934, and entitled Permanent magnet and method of making the same.
The present invention relates to sintered alloys containing a readily oxidizable element and more particularly to sintered permanent magnets of the type disclosed in Mishima Patents 2,027,994 to 2,028,000 inclusive, and in Ruder Patents 1,947,274 and 1,968,569 and to a method of making the same.
Permanent magnet alloys of the type disclosed in the Mishima and Ruder patents contain iron, nickel and aluminum as the basic or essential ingredients. However, it is well known to include other elements such as cobalt, copper, silicon, titanium, chromium, molybdenum, tungsten and manganese in the alloys if desired and as indicated in the above patents. Preferred permanent magnet compositions are those containing about 6 to aluminum, 17 to 35% nickel with the remainder iron; or 6 to 15% aluminum, l2 to 35% nickel, an appreciable quantity up to 18% cobalt with the remainder iron; or an alloy disclosed in Ruder application Serial No. 96,854 filed August 19, 1936, which may consist of about 14 to 25% nickel, about 8 to 13% aluminum, about 2 to 18% cobalt, about 2 to 16% copper with the remainder iron.
In the manufacture of alloys of the above type, it has been customary to melt the ingredients of the alloy and cast the molten metal in molds. After castings have been made they generally are normalized by heating at a temperature above 1000 C. but not materially higher than 1400 C. after which they are quenched and reheated between about 600 C. and 700 C. to eiect ageing Magnets made in accordance with this process have highly desirable magnetic characteristics but are hard and brittle. Such magnets cannot be machined and usually require considerable finish grinding.
Prior to the present inventionattempts have been made to press and sinter metal compositions containing aluminum but such processes, in general, have been unsuccessful owing to the ease with which aluminum is oxidized. For example, if a, mixture of powdered iron, nickel, and aluminum comprising ingredients as disclosed in the Ruder and Mishima patents is pressed in a mold and then sintered, it will be found that even when the sintering is carried out in hydrogen which has been purified and dried by means heretofore employed for that purpose the resulting product is a swollen mass lacking coalescence due to the very (Ci. 'i5-22) pronounced ainity of the finely divided aluminum particles for oxygen. 1 A One of the objects of the present invention is to provide a hard, dense, sintered alloy containing a readily oxidizable ingredient such as aluminum. It is also an object of the -invention to provide a continuous method for producing sintered alloys containing aluminum as one of the principal ingredients. It is a further object of ythe invention to provide permanent magnets of the composition disclosed in the above noted Ruder and Mishima patents which will require a minimum of finish grinding, which shall be fine grained, uniform in character and have a high tensile and transverse strength as well as highly desirable permanent magnet characteristics. Other objects will appear hereinafter.
The novel features which are characteristic of my invention will be-set forth with particularity in the appended claims. 'I'he invention itself, however, will best be understood by reference to the following specification when considered in connection with the accompanying drawing in which Fig. 1 is a view in elevation of a hydrogen furnace which may be employed in carrying my invention into effect; Fig. 2 is a longitudinal sectional view, broken away and on an enlarged scale, of the apparatus disclosed in Fig. 1; Fig. 3 is anend view of the apparatus shown in Fig. 2, while Fig. 4 is a perspective view of a boat employed in the operation of the furnace and adapted to hold the material to be sintered.
In manufacturing sintered magnet alloys containing iron, nickel .and aluminum as essential ingredients, the process which I employ may or may not be continuous. In both processes, however, oxidation of the aluminum content of the alloy may be avoided by the use of a foundation alloy. The foundation alloy preferably is a very brittle iron-aluminum alloy which consists of about 50% aluminum and 50% iron, and contains all the aluminum present in the final alloy.l In making the foundation alloy the necessary quantity of iron, which may comprise several pieces of ordinary melting stock, is heated in a high frequency induction or other suitable furnace to an elevated temperature, for example, a temperature in the neighborhood of 1000 C. This temperature is several hundred degrees below the melting point of iron but is suiiiciently high to permit alloyage of aluminum with iron. Aluminum, which likewise may comprise several pieces of ordinary melting stock, is added to the iron to form an alloy consisting substantially of 50% iron and 50% aluminum. The molten alloy is poured into a graphite or other suitable mold to solidify. The alloy thus produced is very brittle and may be crushed easily, it also remains stable; that is, it does not disintegrate physically when exposed to atmospheric conditions.
In fabricating the magnetic alloy the foundation alloy is crushed to the desired extent and added to the other nely divided ingredients present in the magnetic alloy, for example, iron and nickel, or iron, nickel and cobalt, etc., to provide the desired alloy composition. The finely divided materials are mixed, usually in a ball mill, for about iive hours and then pressed into a desired shape in a steel mold. The pressed mixture may then be placed in a closed tube having a small outletopeningat one end. The tube Vis supplied with pure dry hydrogen or other reducing gas, positioned in ahydrcgen furnace, and sintered at a temperature above 1000 and preferably at about 1400" C. The time required to complete the sintering action may vary from about one-half to iive hours depending upon the load and size of the pieces to be sintered.
After the material has been sintered into a hard, dense mass, it preferably is normalized by heating for about one hour at a temperature above 1000". C. but not materially higher than 1400" C. and preferably at a temperature of about 1050 to about 1100 C. No advantage is obtained by employing a normalizing temperature materially higher than about 1l00 C. Any red furnace may be employed in the normalizing operation since the sintered alloy does not tend to become appreciably oxidized. The alloy may be cooled from the normalizing temperature in still air although, under certain circumstances, the cooling may be accelerated by means of an air blast or slowed down by cooling a plurality of parts in contact with one another. Also parts of small cross sections that would cool too fast in still air can be retarded to a proper rate of cooling by introduction into an air furnace running at about 500 to 600 C.
The copending application of William E. Ruder, Serial No. 758,441, filed December 20, 1934. discloses that for the production of alloys having the best permanent magnet qualities, therate employed in cooling the magnet material from the sintering or normalizing temperature to about 500 C. will vary with the composition and the size of the magnet alloy pieces: also that the magnetic properties of the nished alloy such as residual and coercive force may be varied by varying the cooling rate. For example, alloys consisting of iron. nickel and aluminum should be cooled from the normalizing temperature to about 500 C. at about 400 to 600 C. per minute, and preferably at about 500 C. per minute, While alloys consisting of iron. nickel, aluminum and cobalt should be cooled at a slower rate. for example 175 to 325 C. per minute. and preferably at about 250 C. per minute. The cross section of the magnetic material determines to some extent the cooling rate to be employed. For example, a bar consisting of iron, nickel, aluminum and cobalt about one-cuarter inch square preferably should be cooled in still air to obtain the best magnetic qualities, while bars of the same composition and about one-half inch souare should be cooled in moving air. If bars of the same composition are about one inch square and over they should be cooled in an air blast or in an air blast moistened with a cooling medium.
The permanent magnet properties of the alloy vary with the rate of cooling from the normalizing temperature. For example, an iron, nickel, aluminum alloy one-quarter inch by onehalf inch in cross section cooled in an air-blast at the rate of about 600 C. per minute has a residual of about 6900 and a coercive force of about 445. The same cooling rate applied to an iron, nickel, aluminum, cobalt alloy of the same cross section gives a residual of 8100 but a low coercive force of about 315. The same iron, nickel, aluminum. cobalt alloy Vof the same dimensions when cooled at a slower rate, as in still air, has a residual of 7800 and a coercive force of about 360. With a further decrease in the cooling rate, for ex ample with two bars in contact with one another, a residual of 7400 and a coercive force of 435 may be obtained. By selecting a proper cooling rate, it is possible to secure a wide range of residual and coercive force, and if residual is more important than coercive force in an iron, nickel, aluminum, cobalt alloy, it should be cooled more rapidly than would be the case if coercive force were the more important.
If desired the alloy may be cooled at the desired rate directly after the sintering operation and the normalizing treatment omitted without impairment of the magnetic properties of the alloy. Such a process however is not as satisfactory economically as the process employing the normalizing step. For example, in cooling the alloy directly from the sintering temperature the container with the sintered material therein may be removed from the furnace and the sintered material taken out of the container while the container is at an elevated temperature. Under such circumstances the interior of the container will become oxidized and the oxide coating must be removed before the tube is again used for the sintering operation. If the container and load therein are removed from the furnace and allowed to cool to room temperature the rate of cooling may be too slow due to the bulk of the container and the load therein. These difficulties are avoided when the normalizing step is employed since there is no danger of oxidizing the sintered alloy. It is preferable therefore always to normalize the alloy unless the continuous process hereinafter disclosed is employed.
If the alloy, after sintering or normalizing, is cooled in air at the proper rate for that alloy the optimum atomic arrangement for best permanent magnet properties is obtained so that reheating of the material at temperatures between about 500 C. and 700 C.'at the end of cooling period to eifect ageing or precipitation may be omitted if desired.
Although I have referred to cooling in air after the sintering or normalizing treatment, my invention is not limited to cooling in any particular atmosphere. If desired, the cooling action may be carried out in substantially any gaseous medium without adversely affecting the magnetic or physical properties of the material, for example in the cooling chamber of the ordinary hydrogen furnace. Where I employ the expression cooling in air in the specification or claims, I have reference to a type of cooling rather than to cooling in a certain gaseous medium.
The sintered alloy containing iron, nickel, and aluminum as basic ingredients may be machined. However, in general, it will be found easier to carry out any desired machining operation either on the material as pressed and before sintering, or on the pressed and partly sintered material. In the latter case the material which has been mixed and pressed, as heretofore pointed out, is heated at a temperature oi about 600 C. for about one hour in a hydrogen or other suitable reducing atmosphere to effect partial sintering. It is then cooled rapidly, preferably in the cooling chamber of the furnace, to prevent oxidation of the iron, nickel and aluminum.
In the partial sintering operation, it is not necessary to employ a pure dry hydrogen atmosphere. Ordinary line hydrogen, which contains some moisture, may be employed since the ferroaluminum foundation alloy employed in making the magnetic alloy is not oxidized in such an atmphere at 600 C. Material which has been partially sintered may be machined readily. Moreover, the partial sintering action does not adversely aect the magnetic properties of the iinished magnets. Material which has been partially sintered and then machined should, of course, be sintered thereafter at a temperature above 1000 C. and preferably at about 1400 C.
and then cooled at the proper rate, or reheated to effect precipitation, as hereinbefore indicated.
In quantity production of permanent magnet alloys of the Ruder and Mishima. type, I prefer to employ a continuous process in which sinterlng and precipitation may be effected without any reheating. In carrying out my improved process, I may employ a modified form of hydrogen furnace i. The furnace comprises the usual heating chamber 2, supplied With hydrogen gas through the pipe An elongated rectangular shaped steel tube l, which extends through and beyond each .end of the heating chamber of furnace i, comprises a heating or sintering chamber 5 coextensive with the heating chamber 2, and a cooling chamber 6 which forms an extension of the sintering chamber 5. The inlet and outlet ends of tube S are provided with doors or closure members l and 8 respectively.y Outlet door is provided with an opening il which in the present case is about .040" in diameter, while the inlet door ll is provided with .an opening l about .052" in diameter. Slotted pipes i l and l2, positioned beneath these doors, supply a curtain of hydrogen over the ends of the tube l and prevent access of air, particularly by convection, to the interior of the tube when either door is opened. The portion of the .tube El comprising the cooling chamber 6 is cooled by a water jacket i3, having an inlet pipe l0 and an outlet pipe l5 for the circulation of a cooling medium therethrough.
In operation the tube i is heated to a temperature above 1000 C. and preferably at about 1400 l C. by means of the usual heater coil it. Hydrogen, which preferably has been purified and dried to remove moisture therefrom, lis supplied to the tube at a point between the heating and cooling zones through a pipe il. As the hydrogen enters tube d it divides. One part flows towards the outlet opening 9, while the remainder and greater portion ows towards and out of the larger opening I0 in the closure member l. Ordinary line hydrogen may be supplied to the heating zone 2 of the furnace I through pipe 3. This hydrogen is burned as it emerges from the opening i8, while the hydrogen intube d is burned as it emerges from openings 9 and I0. 'I'he pieces of material I9 to be sintered are positioned on metal boats 20 which are pushed slowly through tube 4 by means of a rod 2l operated by a driving device 22.
That portion of the hydrogen in tube 4 which' ows towards the opening i0 comes in contact with the sintered pieces emerging from the.
hottest zone in the furnace. At this temperature, about 1400 C., the purified hydrogen is further purified by the removalof substantially all traces of oxygen therefrom. No reaction to form water takes place, however, as the surface of the sintered material, in this case, permanent magnet material containing as essential ingredients, iron,
nickel, and aluminum, is practically inert to re- In a 4 furnace of the type disclosed and havingoutlets as designated, the magnetic properties of sintered alloy are progressively improved as the hydrogen ow is increased from about 4 to 10 cubic feet per hour. Although freshly hydrogen cleaned, powdered materials aire employed in fabricating the alloys, some degree of oxidation of the powdered materials occurs during mixing and pressing. However, since the relatively large hydrogen discharge opening is at the inlet end of the tube d, the hydrogen iiow is in the proper direction to maintain an extremely high degree of purity at the inlet point of tube l*l where the demand is most critical.
The time required for a boat 20 to pass through the heating zone in the tube i usually varies from about one-half to two hours depending upon the size of the pieces to be sintered. The temperature of the hot zone grades off from about 1400" C. at the center to about 1050 C. to 1150 C. at the end adjoining the cooling chamber. As a boat approaches the end of the hot zone 5 the outlet door 8 is opened and the operator inserts a rod and pulls the boat quickly into the cooling chamber 6, Where the sintered material is permitted to cool below 600 C. The cooling period, usually varies from about 10 to about 30 minutes according to the composition, size of pieces i9, and magnetic properties desired. The cooling rate may be co-ntrolled by varying the rate of ow of the cooling medium in water jacket I3.
'I'he material carried on the fore-end of the rst boat load which is passed through the sintering chamber may under some conditions be oxidized. To avoid any spoilage of good material, it is advisable to push through the tube d, a preliminary load of scrap material which will serve to clean up the hydrogen in preparation for succeeding loads.
'I'he atmospheric conditions in the hot section of the sintering section of tube i are ideal for causing sticking of the boats to the tube d owing to the reducing action of the hydrogen and the high temperature employed. To avoid such action a. composite type of boat 20 may be employed. In constructing the boats, iron powder is mixed with a smaller quantity of aluminum oxide powder, for example about 75% iron and about 25% aluminum oxide and spread into a relatively thin even layer having the surface dimensions desired for the finished part. A second and thicker layer of powdered iron is then superimposed on the first mentioned layer and the two layers pressed together in a mold and then sintered for about two hours at about 1450 C. Two or more metal pieces thus fabricated may be readily welded together, owing to the presence of the iron layer, to provide boats of any desired width. End pieces 23 having the oxide-iron mixture on the outside are welded to the base portion of the boat. A boat may be pressed entirely of the 25 A1203- 75 Fe mixture but such material cannot be welded and unless a. large enough mold is available to press a complete boat it is necessary to use pieces of composite construction having weldable material on one side. Another advantage in using a composite boat is that any deformation of the boat due to alternate heating and cooling may be removed by cold pressing without danger of breakage or oxidation.
I prefer to employ a mixture of about 75% iron and 25% aluminum oxide in the construction of the boat 20 but these percentages are not critical and may be varied to a considerable extent. Furthermore, I may, if desired, employ in the construction of the boats a mixture of aluminum oxide or any other inert oxide with metals other than iron. For example, if unusually high temperatures are to be employed in the sintering operation, metals such as tungsten and the like may be employed to replace the iron in whole or in part.
Although I prefer to make sintered material in accordance with the process hereinbefore set forth in which a foundation alloy of 50% iron and 50% aluminum is first produced and thereafter pulverized and mixed with the desired quantity of iron and nickel or other powdered ingredients of the alloy and then pressed into shape, it is possible by the use of certain precautionary measures to avoid the formation of a foundation alloy o-f iron and aluminum and to make the nished product by mixing powdered iron, nickel and aluminum in the desired proportions. These precautionary measures comprise the use of very pure ingredients, particularly pure iron; the use of a Very ne and dense aluminum; the proper control of gas flow; and the use of hydrogen having a degree of purity substantially equal to that of the hydrogen flowing through the hot zone of the tube in the above continuous process. The product obtained by mixing and pressing powdered iron, nickel, and aluminum, or other similar mixtures containing aluminum, and thereafter sintering in a hydrogen atmosphere is substantially as good magnetically and in appearance as that obtained when a foundation alloy of iron and aluminum is employed in fabricating the alloy.
The finished sintered alloy has permanent magnet properties equal to those of an alloy of the same composition made by casting and heat treating. In addition, the sintered alloy is fine grained and has tensile and transverse strengths which are respectively ten and ve times greater than the tensile and transverse strengths of cast alloys cf the same composition. Thelsintered alloy requires a minimum of grinding which may be carried out without any danger of cracking the alloy. i Furthermore, if desired, solid or hollow inserts may be made in the pressed material. Under such circumstances however the holes drilled in the pressed material should be slightly larger than the inserts to thereby prevent cracking or distortion when the material is sintered. The sintered product made by the continuous process has the additional advantage of having a very bright finish.
In fabricating the sintered magnetic alloy, the mixed ingredients usually are subjected to a pressure of about 10 to 30 tons per square inch. Material which has been subjected to such pressure shrinks about 6 to 14% during the sintering operation, the greater shrinkage occurring ,With
material pressed at the lower pressures. Notwithstanding such shrinkage, the sintered alloy can be made to very close tolerances, i. e., plus or minus ve mils. Sintered magnets have an additional advantage in economy of material due to the fact that there is no waste material such as the gates and risers which are formed during the process of manufacturing cast materials.
Although the alloy material preferably is shaped by pressure in a steel mold, it also may be formed in some cases by extruding the mixed ingredients with a binder material of which starch is an example. The extruded material may then be heat treated as hereinbefore set forth.v
While I prefer to employ a foundation alloy consisting of about 50% iron and about 50% aluminum, other percentages of iron and aluminum may be employed in the fabrication of the foundation alloy. Also, the foundation alloy may be formed by alloying the aluminum with either cobalt or nickel, or with iron and cobalt in Various percentages. However, although various foundation alloys containing the aluminum may be employed, the alloy consisting of 50% iron and 50 aluminum is, in general, the most satis factory owing to the low temperature at which it can be manufactured and the ease with which it may be crushed.
While my invention relates more particularly to permanent magnets of the type disclosed in the above-mentioned Ruder and Mishima patents, it is not restricted to alloys of that type. For example, oxidation resistant alloys containing iron, aluminum and chromium may be formed either by pressing a mixture of the powdered elements and then sintering itin a hydrogen furnace as hereinbefore set forth, or by first making a base or foundation alloy of iron and aluminum, as also hereinbefore set forth, and then crushing the foundation alloy, mixing it with the chromium and the remainder of the iron, pressing the mixture into a desired shape and then sintering the shaped material. Such alloys when made by melting and casting are very brittle but when fabricated in the manner indicated above they are ductile and when employed as resistance wire have a far longer life at temperatures of say 1200 C. than wire containing the same ingredients and made from cast material. A
What I claim as new and desire to secure by Letters Patent of the United States is:
1. The process of making an alloy which if made by a casting process would be very brittle by reason of the presence therein of a readily oxdizable metal, said process comprising making a foundation alloy containing said readily oxidizable metal and at least one other ingredient of said alloy, pulverizing said alloy casting, and pressing and sintering it with the other ingredients of said alloy.
2. The process of making a ferrous alloy which contains suflicient aluminum to make it very brittle and unmachinable if made by casting, said process comprising pulverizinga foundation alloy casting consisting substantially of all the aluminum and at least one other ingredient of said alloy, pulverizing said alloy casting, mixing said pulverized material with the other ingredients of said alloy, pressing the mixture into a desired shape, heating the pressed material at a temperature above 1000o C. and cooling it.
3. The method of making a magnetic alloy consisting substantially of iron, aluminum and metal from a group consisting of nickel and coamarsi balt which comprises alloying the aluminum with a portion of the iron to provide a foundation alloy consisting of about 50% aluminum and 50% iron, pulverizing said alloy and mixing it with the remaining ingredients present in the final alloy, pressing and sintering the mixed powdered materials, normalizing the sintered product at a temperature of about 1050 C. and air cooling from the normalizing temperature.
4. The method of makinga magnetic alloy containing aluminum and iron which comprises forming a casting containing about 50% aluminum and 50% iron, pulverizing said casting, mixing said pulverized material with the other ingredients of said alloy, pressing the mixture into a desired shape, sintering the pressed material at a temperature above 1000 C. and air cooling the sintered material.
5. The method of making a sintered alloy which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving said pressed material through the heating zone of a furnace to thereby sinter said alloy and suddenly removing the sintered alloy from said heating zone to a controlled cooling zone the rate of cooling employed in said cooling zone eecting precipitation in said alloy.
6. The method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the mixed powdered ingredients comprising the alloy into a desired shape, continuously moving a series of boats containing said pressed material through a hydrogen furnace heated to a temperature of about 1400 C. and in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy.
'7. The method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the mixed powdered ingredients comprising the alloy into a desired shape, moving the pressed material through the heating zone of a hydrogen furnace in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy, and suddenly moving the sintered material from the heating zone into the cooling zone of said furnace the rate of cooling employed in said cooling zone eilecting precipitation in said alloy. 1
8. The method of making a sintered alloy containing a readily oxidizable metal which comprises pressing the powdered ingredients comprising the alloy into a desired shape, moving the pressed material through the heating zone of a hydrogen furnace in the opposite direction to the flow of hydrogen therein to thereby sinter the alloy, and cooling the alloy in a current of hydrogen having a direction of flow which is opposite to that of the hydrogen in said heating zone.
9. The method of making an alloy containin iron, nickel and aluminum as basic ingredients which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving the pressed material through the heating zone of a furnace while said material is in contact with a puried reducing atmosphere to thereby sinter the alloy, suddenly removing the alloy from said heating zone to a cooling zone in said furnace and controlling the temperature of said cooling zone to eiect a condition of precipitation in said alloy.
10. The method of making an alloy containing iron, nickel and aluminum as basic ingredients, which comprises pressing mixed powdered ingredients comprising the alloy into a desired shape, continuously moving the pressed material through a container which extends through the heating zone of a furnace whereby said pressed material may be sintered, surrounding the portion of said container Within said heating zone with a reducing atmosphere. supplying a purified reducing atmospherev to said container, suddenly removing the sintered material from said heating zone to a cooling zone in said container and controlling the temperature of said cooling zone to effect a condition of precipitation in said sintered material.
GOODWIN H. HOWE.
US164354A 1937-09-17 1937-09-17 Method of making a sintered alloy Expired - Lifetime US2192741A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US164354A US2192741A (en) 1937-09-17 1937-09-17 Method of making a sintered alloy
US182087A US2142846A (en) 1937-09-17 1937-12-28 Metallic boat for use in high temperature furnaces
US183146A US2197642A (en) 1937-09-17 1938-01-03 Furnace
US196691A US2192743A (en) 1937-09-17 1938-03-18 Sintered permanent magnet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US164354A US2192741A (en) 1937-09-17 1937-09-17 Method of making a sintered alloy

Publications (1)

Publication Number Publication Date
US2192741A true US2192741A (en) 1940-03-05

Family

ID=22594108

Family Applications (1)

Application Number Title Priority Date Filing Date
US164354A Expired - Lifetime US2192741A (en) 1937-09-17 1937-09-17 Method of making a sintered alloy

Country Status (1)

Country Link
US (1) US2192741A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519502A (en) * 1964-08-04 1970-07-07 Elect & Magn Alloys Res Inst Method of manufacturing sintered metallic magnets
US5520748A (en) * 1993-07-27 1996-05-28 Pohang Iron & Steel Co., Ltd. Process for manufacturing Alnico system permanent magnet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519502A (en) * 1964-08-04 1970-07-07 Elect & Magn Alloys Res Inst Method of manufacturing sintered metallic magnets
US5520748A (en) * 1993-07-27 1996-05-28 Pohang Iron & Steel Co., Ltd. Process for manufacturing Alnico system permanent magnet

Similar Documents

Publication Publication Date Title
US2225424A (en) Manufacture of alloys, in particular steel alloys
US2192743A (en) Sintered permanent magnet
US3150444A (en) Method of producing alloy steel
US2205865A (en) Method of manufacturing alloys, in particular steel alloys
US2342799A (en) Process of manufacturing shaped bodies from iron powders
US2192744A (en) Sintered permanent magnet
US3183127A (en) Heat treatable tool steel of high carbide content
JPH03166335A (en) Dispersively reinforcing material
US2192741A (en) Method of making a sintered alloy
US3658604A (en) Method of making a high-speed tool steel
US2159231A (en) Producing nickel alloy articles
US2352316A (en) Method of producing shaped bodies from powdery ferrous material
US3975193A (en) Powder metallurgy process for producing stainless steel stock
KR960003721B1 (en) Mixed powder for powder metallurgy and the sintered product thereof
US1703416A (en) Metallic article of manufacture
US2159604A (en) Metallic article
US3419383A (en) Producing pulverulent iron for powder metallurgy by multistage reduction
US3752712A (en) Iron copper prealloys
US4069043A (en) Wear-resistant shaped magnetic article and process for making the same
DE10064056B9 (en) A process for producing a sintered body of high-hardness, high-chromium-content cast iron
JP2612419B2 (en) Method for producing powder for MPP core and method for producing MPP core using the powder
US1669649A (en) Magnetic material
US2366371A (en) Powder metallurgy
US3331712A (en) Method of making magnetic material
JPS6314838A (en) Production of fe-si type sintered soft magnetic material