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US3615339A - Process for producing iron powder from hematite ores - Google Patents

Process for producing iron powder from hematite ores Download PDF

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US3615339A
US3615339A US768543A US3615339DA US3615339A US 3615339 A US3615339 A US 3615339A US 768543 A US768543 A US 768543A US 3615339D A US3615339D A US 3615339DA US 3615339 A US3615339 A US 3615339A
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iron powder
reduction
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iron
hematite
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W J Dennis Stone
David Stewart Hay
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W J DENNIS STONE
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    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21B—MANUFACTURE OF IRON OR STEEL
    • C21B15/00—Other processes for the manufacture of iron from iron compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00—Making metallic powder or suspensions thereof
    • B22F9/16—Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/20—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21B—MANUFACTURE OF IRON OR STEEL
    • C21B13/00—Making spongy iron or liquid steel, by direct processes
    • C21B13/006—Starting from ores containing non ferrous metallic oxides
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21B—MANUFACTURE OF IRON OR STEEL
    • C21B13/00—Making spongy iron or liquid steel, by direct processes
    • C21B13/14—Multi-stage processes processes carried out in different vessels or furnaces
    • C21B13/146—Multi-step reduction without melting
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00—Technologies related to metal processing
    • Y02P10/10—Reduction of greenhouse gas [GHG] emissions
    • Y02P10/134—Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen

Definitions

  • ABSTRACT A process for producing iron powder in which a hematite ore concentrate is ground and passed through a highintensity wet magnetic separator to remove silica and other acid insoluble impurities, after which the purified hematite is reduced in the presence of hydrogen to form iron powder.
  • PROCESS FOR PRODUCING IRON POWDER FROM HEMATITE ORES BACKGROUND OF THE INVENTION 1.
  • Field of the Invention The invention relates to a powder.
  • powders produced by the known methods are usually pulverized, screened and blended to assure that they have the desired properties before use.
  • an iron powder to be acceptable for most purposes must conform to the following requirements:
  • the material should be less than 100 mesh in particle size, and a maximum of 60 percent may be less than 325 mesh. Within these limits, the particle size distribution or gradient may vary somewhat, but should be approximately of the order of one-third greater than 200 mesh, one-third greater than 325 mesh, and one third less than 325 mesh.
  • mill scale It is known to produce iron powder by direct reduction of iron oxide and typical sources of this iron oxide include chemically produced oxide, mill scale and natural ore concentrates.
  • the chemically produced oxide is of very high purity but is prohibitively expensive for pressing powders.
  • Mill scale has the obvious disadvantage of only being available in very limited quantities and subject to considerable variations in grade.
  • powder produced from mill scale contains undesirable alloy elements such as manganese, which were in the steel.
  • mill scale must be collected from a large number of sources, which cannot be uniform, and dirt and contamination are picked up during collection in the mill and shipment. This means that extensive cleaning and blending is required before it may be used and, on occasion, as much as 30 percent must be discarded as being unsuitable.
  • lron powder can also be produced by processes other than direct reduction.
  • One such process involves atomizing molten process for producing iron low-carbon steel by spraying. The steel becomes partly oxidized during spraying but depending on the carbon content, more oxide, usually mill scale, is mixed with it. This mixture is then reduced in a furnace, at which time oxygen combines to remove the carbon.
  • This is obviously a relatively complex and expensive process but again the main problem is the source of raw materials. Only scrap is sufficiently cheap to be considered and not all scrap is suitable.
  • the raw material supply is governed independently of the demand for powder.
  • the powder contains the undesirable alloying elements present in the steel.
  • Some iron powder is also produced electrolytically but sells at three times the price of reduced powders so that it can obviously be considered only for very special applications.
  • an iron powder meeting the above requirements can be simply and inexpensively obtained by passing a finely divided natural hematite ore through a high-intensity wet magnetic separator to reduce silica and other acid insoluble impurities therein to preferably less than 0.2 percent and treating the purified hematite obtained with a reducing agent at reducing temperatures below the melting point of iron to produce a substantially pure iron product.
  • the iron product is obtained in the form of an agglomerate of lightly adhering particles which is easily broken down into discrete particles.
  • hematite for the production of iron powder has the great advantages of low cost and unlimited availability. As stated above, it is already known to purify magnetite by magnetic separation but it has been found to be very difficultto obtain a clean separation of magnetite during magnetic separation. Thus, since hematite is considered to be a nonmagnetic material, it could not have been expected that it could be purified magnetically and it is particularly surprising that hematite can be purified in this manner, to the very high degree necessary to permit direct reduction to substantially pure iron. It has also surprisingly been found that the hematite can be initially ground to a particle size range such that after magnetic separation and reduction, iron powder is obtained without further grinding or classifying which is within the commercially acceptable particle size distribution.
  • the reduction can be conducted by means of any of the usual reducing agents, such as solid carbon, gaseous reducing agents such as hydrogen or a mixture of both the solid and gaseous reducing agents.
  • reducing agents such as solid carbon
  • gaseous reducing agents such as hydrogen or a mixture of both the solid and gaseous reducing agents.
  • a wide range of temperatures are possible during reduction with higher temperatures providing a faster reaction rate. Temperatures between l,600 F. and the melting point of iron are preferred and a temperature between 2,000 2,200 F. has been found to be particularly desirable.
  • the reduction can be conducted in any suitable furnace and as indirect gas fired belt furnace has been found to be very satisfactory. According to a preferred procedure both solid carbon and hydrogen gas are used during reduction with the carbon being deposited in finely divided form on the belt under the purified hematite particles. It has also been found to be advantageous to conduct the reduction in a two state operation.
  • the iron product obtained from the reduction furnace was found to be in the form of an agglomerate of loosely adhering particles. This agglomerate. was easily broken down into its component particles.
  • the particles of iron powder obtained from the reduction stage are advantageously subjected to densification to adjust density requirements. This can be conveniently done by impact densification, e.g. in a hammer mill. it has also been found that the agglomerate obtained from the reduction furnace can be fed directly to the hammer mill where the agglomerate is broken down to particle size and the particles are densified in a single operation. When a two stage reduction is used, densification is carried out after each stage.
  • the iron powder obtained by the preferred procedure of this invention which includes the steps of forming the agglomerate of loosely adhering particles and impact densification, has the very important advantage that the particles have sharp edges.
  • sharp-edged particles not only produce a superior sintered product but also provide better green strength.
  • the green strength is a measure of the strength of a compact of iron powder before sintering.
  • the iron powder obtained according to the invention also has a very low silica content, which results in the very desirable property of the powder being soft.
  • a soft powder is highly desirable because it facilitates removal of a molded part from a mold and also decreases the amount of wear on the mold face.
  • EXAMPLE 1 As starting material a commercial specular hematite ore concentrate was used containing 66.2 percent iron, 5.] per cent silica and 0.61 percent alumina. A screen analysis of this ore concentrate is given below in table I:
  • the ore concentrate can be ground to a desired particle size in a ball mill or rod mill.
  • the purified iron oxide was subjected to hydrogen reduction in two stage operation.
  • the reduction was carried out in a belt furnace with indirect gas heating.
  • the theoretically required amount of hydrogen is used i.e. about 25,000 cubic feet per ton of ore.
  • the purified iron oxide was contacted with the hydrogen at a furnace temperature of 2,220 F. and remained in contact with the hydrogen for approximately 4 hours.
  • the partly reduced powder emerging from the furnace was then subjected to densification in a hammer mill and the densitied, partially reduced product had the screen analysis given in table [11 below:
  • the final product contained approximately 0.62 percent by weight of acid insolubles and showed a hydrogen loss of 0.15 percent. Its flow rating was 35 seconds and its apparent density 2.2 grams per cc.
  • the iron powder produced in accordance with this invention was subjected to a series of tests by an independent testing organization.
  • the standard used for comparison was an iron powder available from Hoeganaes Sponge lron Corporation under the trademark Hoeganaes Ancor MH100, which is generally accepted in the industry as the standard.
  • EXAMPLE 2 A sample or iron powder was prepared using the same process as Example 1 with the following properties.
  • EXAMPLE 3 The softness or lack of abrasiveness of iron powder is an important characteristic since it affects the ease with which a molded part can be removed from a mold and also the amount of wear on the mold face. Accordingly, comparative tests were conducted comparing the ejection pressures for iron compacts made with the powder of this invention and l-loeganaes Ancor Mil-400 iron powder.
  • Ejection load Wall pressure contact Weight Dlam., Length, Density, pressure, gm. in. in. g./ec. Lbs. Psi. p.s.i.
  • the iron powder of this invention has appreciably lower ejection and wall contact pressures than the standard iron powder, pressed under the same conditions. This means that the iron powder of the invention ejects more readily and less friction heat is created and this represents a major improvement in iron powder.
  • a process for producing iron powder which comprises passing a finely divided natural hematite ore through a high intensity wet magnetic separator to remove silica and other acid insoluble impurities, treating the purified finely divided hematite with a reducing agent at reducing temperatures below the melting point of iron and collecting the substantially pure iron produce obtained.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)

Abstract

A process for producing iron powder in which a hematite ore concentrate is ground and passed through a high-intensity wet magnetic separator to remove silica and other acid insoluble impurities, after which the purified hematite is reduced in the presence of hydrogen to form iron powder.

Description

United States Patent Inventors W. J. Dennis Stone 253 Westcroit Ave; David Stewart lllny, 355 Penn St, both of Beaconsfield, Quebec, Canada Appl. No. 768,543 Filed Oct. 17,1968 Patented Oct. 26, 1971 Priority Oct. 19, 11967 Great Britain 47738/67 PROCESS FOR PRODUCING IRON POWDER FROM HEMATITE ORES 8 Claims, No Drawings ILLS. Cl 75/0.5 AA lint. Cl BZZi W00 [m [50] Field of Search 75/0.5, 1
[56] References Cited UNITED STATES PATENTS 3,148,972 9/]964 Peras 75/1 3,414,402 12/1968 Volk et al. 75/l 3 ,441 ,401 4/1969 Stone et al 75/1 Primary Examiner-L. Dewayne Rutledge Assistant Examiner-W. W. Stallard Attorney-Fetherstonhaugh & Co.
ABSTRACT: A process for producing iron powder in which a hematite ore concentrate is ground and passed through a highintensity wet magnetic separator to remove silica and other acid insoluble impurities, after which the purified hematite is reduced in the presence of hydrogen to form iron powder.
PROCESS FOR PRODUCING IRON POWDER FROM HEMATITE ORES BACKGROUND OF THE INVENTION 1. Field of the Invention The invention relates to a powder.
2. Description of the Prior Art There has been a rapidly expanding industrial interest in iron powder, particularly for use in powder metallurgy. Powdered metal parts have the advantages of requiring no hightemperature melting furnaces and little or no machining. Moreover, powder formulations can be closely controlled to meet specific needs. One of the newest uses of iron powder is in the molding of gears for automobile transmissions.
For best results in powder-metallurgy processes, the particular size distribution, uniformity and apparent density of the powder must be appropriately controlled within well defined limits. Accordingly, powders produced by the known methods are usually pulverized, screened and blended to assure that they have the desired properties before use. For example, an iron powder to be acceptable for most purposes must conform to the following requirements:
1. It must have an apparent specific gravity between 2.2 and 2.5
2. It must have a flow rate of 40 seconds or less, as determined by the time required for 50 grams to pass through a Hall Flowmeter.
3. The material should be less than 100 mesh in particle size, and a maximum of 60 percent may be less than 325 mesh. Within these limits, the particle size distribution or gradient may vary somewhat, but should be approximately of the order of one-third greater than 200 mesh, one-third greater than 325 mesh, and one third less than 325 mesh.
It is known to produce iron powder by direct reduction of iron oxide and typical sources of this iron oxide include chemically produced oxide, mill scale and natural ore concentrates. The chemically produced oxide is of very high purity but is prohibitively expensive for pressing powders. Mill scale has the obvious disadvantage of only being available in very limited quantities and subject to considerable variations in grade. In addition, powder produced from mill scale contains undesirable alloy elements such as manganese, which were in the steel. Moreover, mill scale must be collected from a large number of sources, which cannot be uniform, and dirt and contamination are picked up during collection in the mill and shipment. This means that extensive cleaning and blending is required before it may be used and, on occasion, as much as 30 percent must be discarded as being unsuitable.
Natural ore concentrates are available in unlimited quantities but these contain as much as 6 percent silica. Magnetites may be processed using conventional magnetic techniques but acceptable separation of the silica from most magnetite ores is almost impossible and few are suitable. Canadian Pat. No. 519,725, issued Dec. 20, 1955 describes a process for producing iron powder from magnetite ore in which the silica is removed by chemical treatment with hydrofluoric acid.
Another process for producing iron powder from magnetite is described in Canadian Pat. No. 527,302, issued July 3, 1956. This process employed magnetic separation to purify the magnetite ore but in order to reduce the silica content to below 0.2 percent by magnetic separation it was necessary to grind the'ore such that over 90 percent was -325 mesh. Since this produced particles too small for iron powder it was necessary to sinter and pregrind the purified material to produce particles which after reduction would meet the requirements of iron powder.
Moreover, it is suggested in Canadian Pat. No. 496,781, issued Oct. 13, 1953 that ores such as hematite should first be converted into magnetites and then concentrated by wet mag netic separation.
lron powder can also be produced by processes other than direct reduction. One such process involves atomizing molten process for producing iron low-carbon steel by spraying. The steel becomes partly oxidized during spraying but depending on the carbon content, more oxide, usually mill scale, is mixed with it. This mixture is then reduced in a furnace, at which time oxygen combines to remove the carbon. This is obviously a relatively complex and expensive process but again the main problem is the source of raw materials. Only scrap is sufficiently cheap to be considered and not all scrap is suitable. Here again the raw material supply is governed independently of the demand for powder. In addition, the powder contains the undesirable alloying elements present in the steel.
Some iron powder is also produced electrolytically but sells at three times the price of reduced powders so that it can obviously be considered only for very special applications.
Thus, it will be seen that up until now iron powder has not been available in unlimited supplies at a low cost because of the short supply of the raw material from which it could be produced and/or because of the cost of production.
SUMMARY OF INVENTION According to our invention, an iron powder meeting the above requirements can be simply and inexpensively obtained by passing a finely divided natural hematite ore through a high-intensity wet magnetic separator to reduce silica and other acid insoluble impurities therein to preferably less than 0.2 percent and treating the purified hematite obtained with a reducing agent at reducing temperatures below the melting point of iron to produce a substantially pure iron product. The iron product is obtained in the form of an agglomerate of lightly adhering particles which is easily broken down into discrete particles.
The use of hematite for the production of iron powder has the great advantages of low cost and unlimited availability. As stated above, it is already known to purify magnetite by magnetic separation but it has been found to be very difficultto obtain a clean separation of magnetite during magnetic separation. Thus, since hematite is considered to be a nonmagnetic material, it could not have been expected that it could be purified magnetically and it is particularly surprising that hematite can be purified in this manner, to the very high degree necessary to permit direct reduction to substantially pure iron. It has also surprisingly been found that the hematite can be initially ground to a particle size range such that after magnetic separation and reduction, iron powder is obtained without further grinding or classifying which is within the commercially acceptable particle size distribution.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The reduction can be conducted by means of any of the usual reducing agents, such as solid carbon, gaseous reducing agents such as hydrogen or a mixture of both the solid and gaseous reducing agents. A wide range of temperatures are possible during reduction with higher temperatures providing a faster reaction rate. Temperatures between l,600 F. and the melting point of iron are preferred and a temperature between 2,000 2,200 F. has been found to be particularly desirable.
The reduction can be conducted in any suitable furnace and as indirect gas fired belt furnace has been found to be very satisfactory. According to a preferred procedure both solid carbon and hydrogen gas are used during reduction with the carbon being deposited in finely divided form on the belt under the purified hematite particles. It has also been found to be advantageous to conduct the reduction in a two state operation.
The iron product obtained from the reduction furnace was found to be in the form of an agglomerate of loosely adhering particles. This agglomerate. was easily broken down into its component particles.
The particles of iron powder obtained from the reduction stage are advantageously subjected to densification to adjust density requirements. This can be conveniently done by impact densification, e.g. in a hammer mill. it has also been found that the agglomerate obtained from the reduction furnace can be fed directly to the hammer mill where the agglomerate is broken down to particle size and the particles are densified in a single operation. When a two stage reduction is used, densification is carried out after each stage.
The iron powder obtained by the preferred procedure of this invention, which includes the steps of forming the agglomerate of loosely adhering particles and impact densification, has the very important advantage that the particles have sharp edges. Thus, sharp-edged particles not only produce a superior sintered product but also provide better green strength. The green strength is a measure of the strength of a compact of iron powder before sintering.
The iron powder obtained according to the invention also has a very low silica content, which results in the very desirable property of the powder being soft. A soft powder is highly desirable because it facilitates removal of a molded part from a mold and also decreases the amount of wear on the mold face.
The invention will now be illustrated by the following examples:
EXAMPLE 1 As starting material a commercial specular hematite ore concentrate was used containing 66.2 percent iron, 5.] per cent silica and 0.61 percent alumina. A screen analysis of this ore concentrate is given below in table I:
TABLE 1 Mesh by weight 6+l0 3.7 l+20 23.2 2+35 38.1 -35+65 22.8 65+l00 5.6 l00+l 50 4.2 l50+200 1.3 200+325 0.6 -325 0.1
If necessary, the ore concentrate can be ground to a desired particle size in a ball mill or rod mill. V
The ore concentrates was passed through a Jones high-intensity wet magnetic separator to obtain an iron oxide powder containing less than 0.2 percent by weight of acid insolubles. A screen analysis of the purified iron oxide powder is given in table II below:
The purified iron oxide was subjected to hydrogen reduction in two stage operation. The reduction was carried out in a belt furnace with indirect gas heating. For the reduction approximately two times the theoretically required amount of hydrogen is used i.e. about 25,000 cubic feet per ton of ore.
The purified iron oxide was contacted with the hydrogen at a furnace temperature of 2,220 F. and remained in contact with the hydrogen for approximately 4 hours. The partly reduced powder emerging from the furnace was then subjected to densification in a hammer mill and the densitied, partially reduced product had the screen analysis given in table [11 below:
TABLE I11 Mesh I: by weight +65 65+80 +l00 2.1 l00+l50 23.2 l50+200 22.7 200+270 22.6 270+32$ 8.4 -325 21.0
TABLE IV Mesh k by weight 80+l00 0.6 l00+l50 22.9 l50+200 26.6 ZOO-+270 25.1 -270+325 8.6 -325 16.2
, The final product contained approximately 0.62 percent by weight of acid insolubles and showed a hydrogen loss of 0.15 percent. Its flow rating was 35 seconds and its apparent density 2.2 grams per cc.
The iron powder produced in accordance with this invention was subjected to a series of tests by an independent testing organization. In these the standard used for comparison was an iron powder available from Hoeganaes Sponge lron Corporation under the trademark Hoeganaes Ancor MH100, which is generally accepted in the industry as the standard.
Compaction tests were conducted on the two samples with each being compacted at 30 and 50 tons per square inch with 0.75 percent stearate lubricant. The samples were sintered in dissociated ammonia at 2,050 F. for 45 minutes.
The results of physical tests on these samples were as follows:
EXAMPLE 2 A sample or iron powder was prepared using the same process as Example 1 with the following properties.
Apparent Density, gJcc. 2.41 Flow, sec. 25.0 Screen analysis 91:
+100 mesh 1.4 l+l 50 14.8 -l 50+200 25.9 -200+270 15.5 -270+325 17.6 325 24.8 Average Particle Size, microns 23.5 Weight Loss in Hydrogen.
(l,150C.-l hour) 0.18
Comparative physical tests were conducted on the above sample and a corresponding sample of Hoeganaes Ancor Ml-l-IOO. The samples were each compacted at 30 tons per square inch with 0.75 percent zinc stearate lubricant and were sintered in dissociated ammonia at 2,050 F. for 45 minutes. The results of tests on the sintered samples are as follows:
Product of Hoeganaes Invention Ancor NIH-100 Green Density, glee. 6.!3 6.26 Green Strength. psi. 2150 1850 Sintered Density, glee. 6.12 6.25 Change in Length on Sintering, i: 0.l8 0.l3 Tensile Strength, p.s.i. 18,800 16,800 Elongation, in 1 inch 10.0 8.2 Rockwell Hardness 11,,65 R 66 This test shows an improvement over the standard iron powder not only in tensile strength and elongation but also in green strength.
EXAMPLE 3 The softness or lack of abrasiveness of iron powder is an important characteristic since it affects the ease with which a molded part can be removed from a mold and also the amount of wear on the mold face. Accordingly, comparative tests were conducted comparing the ejection pressures for iron compacts made with the powder of this invention and l-loeganaes Ancor Mil-400 iron powder.
The powders were compacted in 11 inch cylindrical dies with a compacting pressure of 50 tons per square inch. The results were as follows:
Ejection load Wall pressure contact Weight, Dlam., Length, Density, pressure, gm. in. in. g./ec. Lbs. Psi. p.s.i.
Iron powder of invention plus zinc stcarate 90. 1.005 1. 008 6. 93 8, 225 10, 360 2, 580 90. 75 1. 005 1. 006 6. 92 9, 000 11, 330 2, 830 90.41 1.005 1. 003 6. 92 12,000 15, 3 790 Hoeganaes Ancor MH-IOO plus zinc stcarate l i erage.
From the above results it will be seen that the iron powder of this invention has appreciably lower ejection and wall contact pressures than the standard iron powder, pressed under the same conditions. This means that the iron powder of the invention ejects more readily and less friction heat is created and this represents a major improvement in iron powder.
What we claim as our invention is:
1. A process for producing iron powder which comprises passing a finely divided natural hematite ore through a high intensity wet magnetic separator to remove silica and other acid insoluble impurities, treating the purified finely divided hematite with a reducing agent at reducing temperatures below the melting point of iron and collecting the substantially pure iron produce obtained.
2. A process according to claim 1 wherein the purified hematite contains less than about 0.2 percent by weight of silica and other acid insoluble impurities.
3. A process according to claim 1 wherein the reducing agent is a reducing gas containing free hydrogen.
4. A process according to claim 3 wherein a carbonaceous reducing agent is also used.
5. A process according to claim 3 wherein the reduction is conducted in two stages.
6. A process according to claim 3 wherein the reduction is conducted at temperatures within the range of l,600 F. to the melting point of iron.
7. A process according to claim 6 wherein the reduction is conducted at a temperature of 2,000 2,200 F.
8. A process according to claim 3 wherein the iron is obtained from the reduction zone in the form of a mass of loosely adhering particles which are separated into discrete particles and densified by means of impact densification.

Claims (7)

  1. 2. A process according to claim 1 wherein the purified hematite contaiNs less than about 0.2 percent by weight of silica and other acid insoluble impurities.
  2. 3. A process according to claim 1 wherein the reducing agent is a reducing gas containing free hydrogen.
  3. 4. A process according to claim 3 wherein a carbonaceous reducing agent is also used.
  4. 5. A process according to claim 3 wherein the reduction is conducted in two stages.
  5. 6. A process according to claim 3 wherein the reduction is conducted at temperatures within the range of 1,600* F. to the melting point of iron.
  6. 7. A process according to claim 6 wherein the reduction is conducted at a temperature of 2,000* - 2,200* F.
  7. 8. A process according to claim 3 wherein the iron is obtained from the reduction zone in the form of a mass of loosely adhering particles which are separated into discrete particles and densified by means of impact densification.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4227166A (en) * 1977-06-08 1980-10-07 Nippon Kinzoku Co., Ltd. Reactor
US4272749A (en) * 1976-08-09 1981-06-09 Nippon Kinzoku Co., Ltd. Reactor core of insulated iron powder
US6051203A (en) * 1996-04-30 2000-04-18 American Scientific Materials Technologies, L.P. Thin-walled monolithic metal oxide structures made from metals, and methods for manufacturing such structures
CN112267003A (en) * 2020-09-24 2021-01-26 山东鲁银新材料科技有限公司 Preparation method of water atomized pure iron powder with ultrahigh cleanliness, low oxygen and high performance
US11612769B2 (en) * 2017-09-14 2023-03-28 Muniyal Ayurvedic Research Centre Oral health care formulation and method of preparation thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4154608A (en) * 1978-07-19 1979-05-15 Uop Inc. Production of high purity iron powder

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Publication number Priority date Publication date Assignee Title
US3148972A (en) * 1960-03-15 1964-09-15 Renault Method of preparation of pure powdered iron
US3414402A (en) * 1967-06-16 1968-12-03 Hydrocarbon Research Inc Beneficiation of low grade iron ores
US3441401A (en) * 1966-10-26 1969-04-29 Bethlehem Steel Corp Method of removing fatty acid coating from hematite concentrate

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3148972A (en) * 1960-03-15 1964-09-15 Renault Method of preparation of pure powdered iron
US3441401A (en) * 1966-10-26 1969-04-29 Bethlehem Steel Corp Method of removing fatty acid coating from hematite concentrate
US3414402A (en) * 1967-06-16 1968-12-03 Hydrocarbon Research Inc Beneficiation of low grade iron ores

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4272749A (en) * 1976-08-09 1981-06-09 Nippon Kinzoku Co., Ltd. Reactor core of insulated iron powder
US4227166A (en) * 1977-06-08 1980-10-07 Nippon Kinzoku Co., Ltd. Reactor
US6051203A (en) * 1996-04-30 2000-04-18 American Scientific Materials Technologies, L.P. Thin-walled monolithic metal oxide structures made from metals, and methods for manufacturing such structures
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CN112267003B (en) * 2020-09-24 2022-05-03 山东鲁银新材料科技有限公司 Preparation method of water atomized pure iron powder with ultrahigh cleanliness, low oxygen and high performance

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GB1248203A (en) 1971-09-29
FR1587984A (en) 1970-04-03
BE722472A (en) 1969-04-01
DE1803642A1 (en) 1969-06-19

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