US2186659A - Magnetic powder for iron dust cores - Google Patents

Magnetic powder for iron dust cores Download PDF

Info

Publication number
US2186659A
US2186659A US152204A US15220437A US2186659A US 2186659 A US2186659 A US 2186659A US 152204 A US152204 A US 152204A US 15220437 A US15220437 A US 15220437A US 2186659 A US2186659 A US 2186659A
Authority
US
United States
Prior art keywords
powder
particles
iron
magnetic powder
gas
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
US152204A
Inventor
Vogt Hans
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.)
MICRO PRODUCTS Corp
Original Assignee
MICRO PRODUCTS CORP
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 MICRO PRODUCTS CORP filed Critical MICRO PRODUCTS CORP
Application granted granted Critical
Publication of US2186659A publication Critical patent/US2186659A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/20Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of particles, e.g. powder
    • 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
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/06Metallic powder characterised by the shape of the particles
    • B22F1/065Spherical particles
    • 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
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/51Use of fluidized bed in molding
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S75/00Specialized metallurgical processes, compositions for use therein, consolidated metal powder compositions, and loose metal particulate mixtures
    • Y10S75/953Producing spheres
    • 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

Description

Jan. 9, 1940. l H. VOGT 2,186,659
MAGNETIC POWDER FOR IRON DUST CORES Filed July 6, 1937 T 1 El w 1 50 gozo 0 12 24 36 so 72 [k Zwen Zan Patented Jam 9, 1940 STAES PTENT OFFICE MAGNETIC POWDER FOR IRON DUST CORES Application July 6, 1937, Serial No. 152,204 In Germany July 17, 1936 6 Claims.
The present invention relates to a method for the production of magnetic powder which may be suitably compressed to nuclear masses with an insulatory agglomerant having minimum loss at frequencies of about 1000 kilocycles, perferably without setting up an organic insulating film. The purpose of this method is to produce in a specially economic manner this kind of magnetic powder and to obtain the finest quality as regards high-frequency losses and mechanical firmness at the same time. According to the invention. the powder is produced from finely divided alloy consisting of iron with silicon and/0r equivalents which increase the brittleness, hardness and the specific resistance, as e. g. aluminum, in particles of dimensions below 0.02, preferably even less than 0.01 mm. The particles are melted to balls by blowing through a compressed gas flame and collected in a manner that the minuteness of the particles and their spherical form are preserved.
The powdered alloy can be produced chemical- 1y or mechanically to the required fineness and composition. The chemical production can take place, starting with iron as a salt or in the form of an oxide, e. g. Fe,(OH) 2, which is either first reduced and .then mixed, or first mixed with the silicon in powder form and then reduced.
During the heating of the mixture to about 500-700 C. in the presence of hydrogen, the iron is reduced at the same time as the silicon diffuses into the iron. A sintering of the powder does not take place in this process. One can also commence with ground iron powder and alloy it with the silicon as in the above described manner.
In the mechanical comminution of the powder transformer sheet-iron may be utilized, having a .silicon content up to 4% and which can be.
Especiallyhardness and brittleness of the granulated metal are raised considerably and the comminution facilitated. A typical analysis of an original material thus produced is the following:
The impurities contained therein are not only non-injurious, but they actually facilitate pulverization. Methods for the production of this kind of powder by comminution have already been described in applicants copending application Serial Number 61,112, filed January 27, 1936.
Pulverizatiorr takes place effectively by wet or preferably dry mechanical grinding in two runs of a ball mill. In the first run comparatively coarse balls are applied and in the second run much smaller ones. The burden of the mill can 'be increased by forcing a stream of gas through the mechanism and thus the sufl'iciently small ground particles are continuously sifted through the mill. In this manner, the full crushing power of the balls acts upon the particles that are still too large and the cushion effect of the smaller particles is eliminated. In order to avoid undesired reactions (e. g. oxidation) the gas stream can at the same time serve as a protective gas and contains for this purpose hydrogen, nitrogen, illuminating gas, carbonic acid or similar substances. The product coming from the mill is then balled in the compressed gas flame and the balled material is caught in a liquid bath.
By a proper selection of the feed-powder as well as the air-gas proportion, speed and direction, a suitable speed can be imparted to. the particles so that they do not coalesce during flight and the temperature of combustion is increased to such a degree that the particles are melted in the course of their. rapid motion. The flame contains an excess of reducing gases by which the danger of oxidation of the particles is lessened. After melting, the powder can be retained in a vessel heated to 700-900 for a certain time whereby the loss of permeability caused by-cooling of the powder is compensated. The ball-shaped powder can, in addition, be winnowed by air.
The material thus produced is then immediately mixed with the agglomerating agent preferably consisting of artificial resins which can be solidified in such a manner that at least 30% of the volume of the agglomerating agent, preferably in dissolved form, are mixed, i. e. kneaded with the magnetic powder. The compression is then performed in the well-known manner.
The utilization of mechanically ground powder with high silicon content is already known in the Pupin nuclear coils. But such powders were not suitable for the special requirements in high frequency nuclei since they resulted in too high losses on account of their coarse granulation and irregular shape. The applicant has already suggested the utilization of mechanically ground ferric silicide for high frequency purposes. This suggestion did not, however, bring about any successful result because the particles were mechanically rounded. It was found that this mechanical method was insufilcient for the extremely small-sized particles required in high frequency nuclei. It has already been proposed to produce magnetic powder for mass nuclei by reducing iron wire to dust by means of a metal spraying device and conducting it into a cooling medium. In thus reducing the metal there are produced particles of a size which although entirely sumcient for use with Pupin coils are, far too coarse for high-frequency nuclei, causing great loss.
The special advantages derived from the utilization of ferric silicide rounded in the flame were not recognized in this suggestion regarding highfrequency nuclei. The method proposed for the making of glass balls by introducing pulverized material into the flame could not ofier any suggestion for the solution of the present special problem. The manner in which the powder is introduced into the flame outside the burner employed in this method does not permit as even a distribution as is necessary in the present case. It had also to be assumed that the extremely fine iron particles, necessary for high-frequency iron nuclei, would burn up or at least oxidize to a great'degree, or in other respects be affected disadvantageously resulting in a very inferior powder. This opinion is expressed in former works of the applicant in which he suggested that the substance be led through a chamber which is heated externally so as to avoid the direct effect of the flame. But it became evident that in applying this procedure. to industrial mass production, the small particles conglommerated on a large scale, thus giving rise to numerous coarse particles' n the other hand, by merely subjecting the substance to treatment by direct flame, hitherto considered impracticable for such fine powders, balling without agglomeration of the particles is achieved. In all former instructions for thermic balling, knowledge was lacking concerning the true significance of the silicon content in the attaining of the desired result.
Only through the utilization of a substantial silicon content and the brittleness attained thereby is it possible to comminute the particles to a sufliciently fine state bymeans of mechanical grinding. The fineness of the powder thus obtained gives ample insurance against any loss. The suitable range of the size 01 t e particles 18 not increased and the thermic balling improves the quality of the product on account of the higher specific resistance caused at the same time by the high silicon content.
characteristically, all reference as to procedure for the balling of the particles is lacking, especially in the proposals to utilize alloys of supraductility which have a high silicon content in the preparation of nuclear masses. For it was believed that in view of the high internal resistance the increased insulation of the particles, obtainable with particles of round form, was superfluous. This is, in fact, true to a certain extent for with the progressive pulverization to about 20 I get first a certain optimum in regard to the proposed losses. The particles are of completely irregular form and even balling does not result in any improvement.
When the pulverization is continued the powder becomes finer though it becomes electrically inferior. But even the best powder thus obtained is not of the same value as carbonyl iron, which, up to the present, has produced the best nuclei. Inasmuch, then, as the use of even high-siliconcontent alloys and the balling of the particles best obtained thereby, has not resulted in the production of a powder equivalent to carbonyl iron, this method had to be disregarded. In view 01 the high requirements in the selectivity of the receivers which decidedly depend on the degree of loss of the high-frequency iron nuclei, only the nucleus with minimum loss can be considered in the greatest number of cases "applied. Strangely enough, it was found that the passing of the at first inferior, finer powder through a blow-flame does not only make the latter equal in value to the coarser powder, but may even be enhanced in value and become equal in quality to carbonyl iron or even superior to it. Such improvement could not in any Way be expected.
The invention thus rested on the realization that it was possible by means of a definite combination of operations to produce a high-frequency pulverized iron, equal in value at least electrically to carbonyl iron powder, until then resulting in least loss and which is considerably superior to it economically. The advantage derived from my powder consists especially in the possibility of utilizing cheaper parent material together with a simple method of manufacture. But the powder thus produced, owing to its high internal and surface resistance and because of its greater hardness, may be continuously compressed merely by the application of a sufilcient volume of binding media without the additional formation of an'organic insulating film on the individual particles.
The omission of the insulation process means a considerable simplification of manufacture, as well as the elimination of sources of error. Moreover, the nuclei thus produced are especially. firm and mechanically durable. The procedures used one which brings about a considerably greater increase in self-induction when introduced into a slopes entirely downwardly to the right showsthe maximum magnitude of the particles in millimeters indicated by the letters mm. and plotted as ordinates, in relation to the time of pulverization indicated by the letters lb. and plotted as abscissa. The other curve gives the corresponding values of a '0011 indicated by the symbol mL at and plotted as ordinates with a core produced from a powder the particle size of which is plotted as abscissa in terms of the pulverization time corresponding to the particle size. Thus it is evident that a particle size of about 0.015 mm. gives the optimum coil value and that with continued pulverization the coil value not only does not improve, but actually becomes inferior (solid line curve). However, if the particles thus pulverized are led through a blow-flame, we get a sudden increase in coil value, but only in particles of a size less than 0.020 mm. (dotted curve). The increased value thus gained, results in reference to the prepared self-induction coils, in those very values (which are a measure for the value of the coil and therefore for the selectivity of the receivers) which make possible the general application of the nuclei thus produced even demanding the highest quality.
Fig. 2 shows a suitable plant for sifting and thermal balling. The parent powder to be used can be iron powder either mechanically pulverized or' chemically prepared.
According to the arrangement in Fig. 2 the iron powder I is poured into the feeding-funnel 2, supported by means of braces 9, and closed with the cover 3. The powder drops through a shaking sieve 4, driven by motor 6, by means of the eccentrics 5 into the induction tube 1, the bottom of which can be closed by a coarse sieve 36. The size of this sieve 4 and the manner in which shaking takes place regulates the amount of powder passing through the contrivance in a given time. An air-current 29 fiows up through tube. in colliding with the powder which is dropping from tube 1. The powder which is of sufficient fineness is forced by the current of air into tube l8 by way of the annular canal formed at 8.
'The annular cross-section at 8 should not measure more than the internal cross-sections of tube l0, so that no greater velocity of gas results than in tube II). By this means, the
dragging-along of the larger, 1. e. too heavy particles is prevented. The larger, heavier particles fall down rather perpendicularly through tube l0 and through the coarse sieve II and collect at l2. a receptacle l4 by means of a drawing-off mechanism and can be used again in the mill for further comminution. The air current 29 is regulated by means of a gauge IS in the air-pressure tube l1l5. The regulatory gauge l6 can be 75 connected with gauge 19 by means of a coupling From here the particles are emptiedinto rod 20 or similar positive device in such a manner as to result in the same total volumeof flow in any region between the two gauges. In this way, the power of the air-current I I0, determining the maximal size of the particles, can be regulated by valve IS, without affecting the total volume of air forced through the burner.
The air current flowing through gauge l9 can be additionally throttled at 2| forthe purpose of regulating the total volume of air. Then within tube 34, it mingles with the air current carrying the powder flowing through channel l8 and also the fuel gas passing through the regulator 22. The flame 24 is so formed that in a short time it melts the conducted particles into balls. The flame 24 strikes against the water surface found in receptor 23 which is kept at a constant level bymeans of the feed-pipe 25 and overflow tube 26.
The powder I is immediately cooled 011 in this manner and is collected in the lower part of the receptacle 23, from which it can be drawn off by means of the stopcock 28. The powder is thus drawn off into the suction filter below, consisting of receptacle 35, together with filter screen 30 and collecting receptor 32. The moisture adhering to the powder flows through the filter screen and collects in receptor 32, during which process powder I can from time to time be removed from the upper part of receptacle 35. By means of the tube 33, the air below the filter can be withdrawn through suction (vacuum) which hastens the drying process.
The receiving fluid in receptacle 23'may be water to which preferably alkaline ingredients are added. I prefer a. receiving fluid having a pH-value of about 9 to 10; 8 is the lower and 11 the upper limit in most practical cases. The alkaline character may be produced by adding ammonia, soda lye and/or potash lye to the liquid. I contemplate, moreover, to add to the alkaline receiving fluid ingredients acting as reducing agents in alkaline solution. One or more of the known photographic developing substances may be used for this purpose, such as for instance rodinal, pyrogallol, methol and/or hydrochinon and/or formalin. Stabilizators, such as for example sodium carbonate'and/or ammonium carbonate may be added to the reducing agent in order to avoid premature neutralization of the reducing agent.
The powder can now be subjected to an anhealing-treatment for 12-48 hours in vacuo or in nitrogen at temperatures of 700-900" C. which improves its permeability.
The powder thus prepared can then be mixed in a kneading machine with the binding medium, preferably artificial resin that can be solidified amounting to more than 30% by volume, or in dissolved form. After drying the substance is ready to be compressed into high-frequency nuclei of the required shape and in accordance with the well-known method.
The balling process described in this invention, according to which the powder to be bailed is first sifted by means of a gas current and then blown and melted in a compressed gas burner by means of the sifting gas current, may also be.
successfully applied to similar fusible powdered substances. The special method of feeding the powder to the burner by means of the sifting gas current renders possible a very even distribution of the powder. In this way, agglomeration and feeding of quantities that are too large are avoidg5 ed for the burner cannot melt such masses at a sufllcient rate.
'I claim:
1. In a process of producing magnetic powder, the steps which comprise producing a powdered alloy consisting 01. iron and about 5% to 15% of silicon, mechanically disintegrating said alloy to magnetic particles 01' a size less than 0.02 mm., blowing said magnetic particlesthrough a reducing gas flame at a temperature sumcient to melt the particles to spherical form, and cooling down and collecting the particles so obtained. I
2. A process as claimed in claim 1, characterized in that the particles are collected after melting in a receiving fluid consisting essentially of water.
3. A process as claimed in claim 1, characterized in that the particles are collected after melting in a receiving fluid of alkaline nature.
, 4. Aprocess as claimed in claim 1, characterized in that the particles are collected after melting in a receiving fluid of alkaline nature,
containing. ingredients which act as reducing agents in alkaline solution.
5. A process as claimed in claim 1, characterized in that the particles are collected after melting in a receiving fluid of alkaline nature, containing ingredientswhich act as reducing agents in alkaline solution and stabilizators for said reducing agents.
6. In a process of producing magnetic powder, the steps which comprise blowing magnetic particles of a size less than 0.02 mm. through the flame of a gas burner by means of a compressed gas current to which the magnetic powder has been added, said flame being at a temperature sufllcient to melt the particles to spherical form, leading to said burner a parallel gas current which carries no magnetic powder, the proportion of the two gas currents being adjustable while maintaining the gas quantity of the total gas currents constant, and cooling down and collecting the particles so obtained.
HANS VOGT.
US152204A 1936-07-17 1937-07-06 Magnetic powder for iron dust cores Expired - Lifetime US2186659A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2186659X 1936-07-17

Publications (1)

Publication Number Publication Date
US2186659A true US2186659A (en) 1940-01-09

Family

ID=7989130

Family Applications (1)

Application Number Title Priority Date Filing Date
US152204A Expired - Lifetime US2186659A (en) 1936-07-17 1937-07-06 Magnetic powder for iron dust cores

Country Status (1)

Country Link
US (1) US2186659A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2540593A (en) * 1947-12-11 1951-02-06 Standard Oil Dev Co Method of melting reduced metal dust
US2825095A (en) * 1952-05-28 1958-03-04 Int Standard Electric Corp Method of producing highly permeable dust cores
US2909808A (en) * 1954-11-29 1959-10-27 Deutsche Edelstahlwerke Ag Process of producing powdered or granular metallic material
US3001228A (en) * 1959-01-08 1961-09-26 G & A Lab Inc Coating and pelletizing of fusible materials
US3015852A (en) * 1957-04-04 1962-01-09 South African Iron & Steel Process of spheroidizing irregularly shaped particles
US3026568A (en) * 1958-11-14 1962-03-27 Schuller Services Ltd Method for producing coated bitumen pellets
US3036338A (en) * 1959-01-08 1962-05-29 G & A Lab Inc Coating and pelletizing of fusible materials
US3169851A (en) * 1960-02-04 1965-02-16 Union Carbide Corp Process for the oxidation of powders
US3180711A (en) * 1961-06-26 1965-04-27 United Aircraft Corp Scrap recovery device
US3341940A (en) * 1962-03-29 1967-09-19 Philips Corp Method of making a permanent magnet
US3849182A (en) * 1969-06-19 1974-11-19 Xerox Corp Highly shape-classified oxidized low carbon hypereutectoid electrostatographic steel carrier particles
US3923503A (en) * 1973-06-11 1975-12-02 Xerox Corp Electrostatic latent image development employing steel carrier particles
US4299622A (en) * 1978-11-06 1981-11-10 Sony Corporation Magnetic alloy
US4476071A (en) * 1981-12-23 1984-10-09 Swiss Aluminium Ltd. Process for rounding off granular particles of solid material
EP0149027A2 (en) * 1983-12-20 1985-07-24 Wolfgang Seidler Process and apparatus for manufacturing spheroidal metal particles
EP0259844A2 (en) * 1986-09-08 1988-03-16 GTE Products Corporation Fine spherical powder particles and process for producing same

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2540593A (en) * 1947-12-11 1951-02-06 Standard Oil Dev Co Method of melting reduced metal dust
US2825095A (en) * 1952-05-28 1958-03-04 Int Standard Electric Corp Method of producing highly permeable dust cores
US2909808A (en) * 1954-11-29 1959-10-27 Deutsche Edelstahlwerke Ag Process of producing powdered or granular metallic material
US3015852A (en) * 1957-04-04 1962-01-09 South African Iron & Steel Process of spheroidizing irregularly shaped particles
US3026568A (en) * 1958-11-14 1962-03-27 Schuller Services Ltd Method for producing coated bitumen pellets
US3001228A (en) * 1959-01-08 1961-09-26 G & A Lab Inc Coating and pelletizing of fusible materials
US3036338A (en) * 1959-01-08 1962-05-29 G & A Lab Inc Coating and pelletizing of fusible materials
US3169851A (en) * 1960-02-04 1965-02-16 Union Carbide Corp Process for the oxidation of powders
US3180711A (en) * 1961-06-26 1965-04-27 United Aircraft Corp Scrap recovery device
US3341940A (en) * 1962-03-29 1967-09-19 Philips Corp Method of making a permanent magnet
US3849182A (en) * 1969-06-19 1974-11-19 Xerox Corp Highly shape-classified oxidized low carbon hypereutectoid electrostatographic steel carrier particles
US3923503A (en) * 1973-06-11 1975-12-02 Xerox Corp Electrostatic latent image development employing steel carrier particles
US4299622A (en) * 1978-11-06 1981-11-10 Sony Corporation Magnetic alloy
US4476071A (en) * 1981-12-23 1984-10-09 Swiss Aluminium Ltd. Process for rounding off granular particles of solid material
EP0149027A2 (en) * 1983-12-20 1985-07-24 Wolfgang Seidler Process and apparatus for manufacturing spheroidal metal particles
US4627943A (en) * 1983-12-20 1986-12-09 Wolfgang Seidler Process for the production of spherical metallic particles
EP0149027A3 (en) * 1983-12-20 1987-09-02 Wolfgang Seidler Process and apparatus for manufacturing spheroidal metal particles
EP0259844A2 (en) * 1986-09-08 1988-03-16 GTE Products Corporation Fine spherical powder particles and process for producing same
EP0259844A3 (en) * 1986-09-08 1988-09-21 GTE Products Corporation Fine spherical powder particles and process for producing same

Similar Documents

Publication Publication Date Title
US2186659A (en) Magnetic powder for iron dust cores
JP6490259B2 (en) Method for producing Fe powder or alloy powder containing Fe
US3397057A (en) Method for producing flowable metal powders
US3272615A (en) Production of spheroidized particles
CA1235265A (en) Process and apparatus for the production of spherical metallic particles
JP2018186212A (en) Soft magnetic powder, method for manufacturing the same, soft magnetic material, and method for manufacturing powder-compact magnetic core
JPH0211701A (en) Production of fe-si alloy powder
US2990267A (en) Preparation of metal powders
US3597188A (en) Method of making high density iron powder
US2969281A (en) Process for making spherical metal particles
US3128172A (en) Non-spherical cupreous powder
CN109161680B (en) Segregation ore blending sintering method for iron ore
US3881912A (en) Welding filler material
US2721135A (en) Method of producing metallic powders
JPS604891B2 (en) Coarse ore-containing pellets
US3238037A (en) Artificial magnetic oxides
US3383198A (en) High green strength-low density copper powder and method for preparing same
JPS6267102A (en) Production of sintered bronze alloy powder
US2172626A (en) Magnetic material
US2645573A (en) Process for producing brass powder
JPH02263901A (en) Powder for metal injection-molding and manufacture thereof
US2876093A (en) Processes of smelting finely divided iron ore
JPS5953218B2 (en) Hollow spherical iron oxide powder and its manufacturing method
SU1581760A1 (en) Method of preparing charge for producing pellets
SU1082848A1 (en) Method for preparing agglomeration batch