[go: up one dir, main page]

US2104530A - Electric furnace process - Google Patents

Electric furnace process Download PDF

Info

Publication number
US2104530A
US2104530A US113096A US11309636A US2104530A US 2104530 A US2104530 A US 2104530A US 113096 A US113096 A US 113096A US 11309636 A US11309636 A US 11309636A US 2104530 A US2104530 A US 2104530A
Authority
US
United States
Prior art keywords
metal
electrode
core
oxide
cores
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
US113096A
Inventor
Gilbert E Seil
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to US113096A priority Critical patent/US2104530A/en
Application granted granted Critical
Publication of US2104530A publication Critical patent/US2104530A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/52Manufacture of steel in electric furnaces
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Definitions

  • This invention revolves about smelting operations, such as the refining of alloys and relates more particularly to term-alloys including chromium.
  • This reagent is produced by supplying to the bore oi an energized hollow substantially horizontal electrode of an electric furnace having an atmosphere oi carbon monoxide, cores containing comminuted materials capable of yielding under the influence of the heated zone of the electrode,
  • molten metal having a metal oxide dispersed therein, detaining the core materials in the heated zone long enough for the molten metal to attain a temperature substantially above its melting point, to increase the solubility function of the metal for'the metal oxide.
  • FIG. 1 shows in skeleton form the essential parts and elements of an electric furnace suitable for carrying out this invention. Such a furnace is shown in greater detail in my said copending l0 patent application Ser. No. 22,963.
  • Fig. 2 illustrates the novel effects attained by the rotation of the hollow electrodes showing particularly the behavior of the cores due to that rotation;
  • Fig. 3 is a transverse cross sectional View taken along the lines 3-3 in Fig. 2.
  • ill and l 2 indicate substantially horizontal hollow energizable electrodes having adjacent ends it and it respectively for supporting an arc therebetween of sufiicient intensity to heat the region of the arc ends of the electrodes to a. requisite temperature. it indicates a bore of each electrode, and it any suitable mechanism for rotating the electrodes while en- 'ergized.
  • the electrodes are to be housed in an operable electric furnace with usual boundary walls and. top and provided with a hearth ll adapted to hold a bath of molten metal material it having an oxidizable impurity to be refined therefrom and having on the bath a slag it containing oxide material.
  • the reagent 5 is highly oxidizing and includes a metal desirable in the refined metal to be recovered from the bath saturated with a metal oxide dispersed or dissolved therein whose metal also is desirable in the refined metal.
  • the oxide is reduced to metal 40 by the transference of the oxygen thereof to combine with the omdizable impuritypf the bath (such as carbon).
  • the impurity in the form of an oxide departs from the bath of metal being refined as a gas if gaseous, or into the slag if a solid.
  • impurity is carbon, when oxidized it formscarbon monoxide and this, in being continually evolved, forms the atmosphere of the furnace.
  • the reduced metal forms an addition to the metal content of the bath.
  • the cores 20 are composed of comminuted materials comprising those that are translatable under the conditions of temperature obtaining in the heated zone of the electrode, into a metal refining reagent. More particularly those mc.- 55
  • terials can be a metal oxide preferably as an ore; a reducing agent such as carbon in quantity insufficient to reduce all of the metal oxide so that the end product of the reactions in the electrode will be reduced metal and unreduced metal oxide; and a corrective for controlling the passage of the reactive materials through the heated zone of the electrode whereby the reduced metal yield ed therein is retained therein long enough to become superheated high enough above its melting point to become a solvent for the unreduced oxide but below the melting point of the oxide.
  • a satisfactory degree of superheat is of the order of 600 'F. above the melting point of the metal. The result is the emission from the electrode of an oxidizing metal refining reagent.
  • the reduced metal occupies less volume than the constituents which yield it. This causes the cores to become pitted or possessed of pores. The outer surface sections of the cores disintegrate slowly.
  • the drop is not allowed to remain in too long contact with the carbon. Otherwise the metal will stick to the carbon and freeze the core against further forward progress thereof through the bore of the electrode. Such a prolonged contact of the core with one spot in the electrode tends to cause the oxide present in the core to give up some of its oxygen to the carbon of the electrode.
  • the metal oxide usually used in this process is chromium oxide, or an ore containing it such as chromite
  • the reduced chromium being the heaviest constituent of the mass in the electrode tends to settle out and stratify therein whereas it is highly desirable to keep the molten or fiuid constituents in the electrode in well dispersed or mingled condition.
  • the reduced metal such as chromium should stick to the electrode, the carbon thereof being hotter than the metal, will result in a detrimental pick up of carbon by the metal.
  • the space 22 existing be tween the core and the bore, that increases toward the arc end of the electrode, is useful and advantageous because it provides a ready escape for the carbon monoxide of the furnace that is constantly produced due to the oxidation of the carbon impurity of the metal being refined by the oxygen of the oxidizing refining reagent.
  • the step of rotating the electrode serves the several purposes of preventing the reduced metal and its oxide from remaining in fixed relationship with any particular spot in the bore of the electrode; of maintaining the fiuid constituents of the mass in the electrode in intermixed and intermingled condition; and of causing the cores to disintegrate gradually without breaking and thus avoid jamming thereof in the At the same time it assures the disintegration of the cores with the translation of their reactant materials to progress uniformly, dependably and in an orderly manner.
  • the process for modifying the proportion of certain constituents thereof which comprises forming a molten bath of the material to be refined and an oxidizing slag M thereon in a carbon monoxideatmosphere, forming an oxidizing reagent composed essentially of metallic oxide and a reduced metal at a temperature in excess of the melting point oi the reduced metal while conflned'in a substantially horizontal hollow electrode, meanwhile rotating the electrode, supplying a quantity of reagent to the bath for liquid admixture therewith under conditions for inducing an oxidizing action of the reagent upon the oxidizable undesirable constituent of the molten bath by virtue of which the proportion thereof is decreased through conversion into an oxide, and then recovering refined metallic material from the bath.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)

Description

Jan. 4, 1938. G. E. SEIL 2,104,530
ELECTRIC FURNACE PROCESS Filed Nov. 28, 1936 H m II I FIG.
Q INVENTOR GILBERT 5.5511.
a mrm ATTORNEY.
patented Jana ti, iddd I fi th? Claims.
This invention revolves about smelting operations, such as the refining of alloys and relates more particularly to term-alloys including chromium.
i-lleretoiore, I have proposed for this purpose a process, the essence of which is the production within a hollow electrode of a highly oxidizing reagent for use subsequently in admixture in liquid phase with a bath of molten metal to be refined, by virtue of which the oxidizing reagent omdlizes in that hath oxidizrable impurities present therein, coupled with increments to the bath of desirable metal released from the reagent when it gives up its oxygen to the impurity.
This reagent is produced by supplying to the bore oi an energized hollow substantially horizontal electrode of an electric furnace having an atmosphere oi carbon monoxide, cores containing comminuted materials capable of yielding under the influence of the heated zone of the electrode,
molten metal having a metal oxide dispersed therein, detaining the core materials in the heated zone long enough for the molten metal to attain a temperature substantially above its melting point, to increase the solubility function of the metal for'the metal oxide.
When attempt was made to practice this process, disadvantages were experienced under certain conditions in uninterruptedly passing the cores into the bore of the electrode and through the heated zone thereof. So to overcome this is an object of this invention to the end that the functioning of the furnace shall program smoothly and dependably. This object is attained by rotating the hollow electrode while the production oi the refining reagent proceeds therein.
a furnace with these advantages has been devised by me. It forms the subject-matter of my patent application Ser. No. 22,963, filed May 23, 1935. That case is drawn to describe a multiplicity of details of a complete electric furnace including features of construction of electrode carriage, electrode cooling, core feeding mechanisin, and so on. That case has its emphasis directed to apparatus even though it describes a mechanism in which the process of this invention may be carried out. So this case has its emphasis directed toward the process irrespective of the specific apparatus that may be used in its carrylog out. Nevertheless, since everything disclosed in that case is contemplated herein, the priority date of that case will be claimed for this one, on the principle that this is a continuation-in-part of my said earlier application.
Rather than reuse, in reiteration, all of the (or. is-1c) many pages of description and drawings of that case, only that portion thereof is used herein- Which has direct reference to the novel process steps to be claimed in this patent.
The invention hereof is diagrammatically il- 6 lustratedin the accompanying drawing in which,
Figure 1 shows in skeleton form the essential parts and elements of an electric furnace suitable for carrying out this invention. Such a furnace is shown in greater detail in my said copending l0 patent application Ser. No. 22,963.
Fig. 2 illustrates the novel effects attained by the rotation of the hollow electrodes showing particularly the behavior of the cores due to that rotation; and
Fig. 3 is a transverse cross sectional View taken along the lines 3-3 in Fig. 2.
In Fig. l of the drawing, ill and l 2 indicate substantially horizontal hollow energizable electrodes having adjacent ends it and it respectively for supporting an arc therebetween of sufiicient intensity to heat the region of the arc ends of the electrodes to a. requisite temperature. it indicates a bore of each electrode, and it any suitable mechanism for rotating the electrodes while en- 'ergized. The electrodes, of course, are to be housed in an operable electric furnace with usual boundary walls and. top and provided with a hearth ll adapted to hold a bath of molten metal material it having an oxidizable impurity to be refined therefrom and having on the bath a slag it containing oxide material. To the bores of the electrodes are forcibly supplied cores 2!], and from the are ends of the electrodes there fall drops it of the refining reagent. The reagent 5 is highly oxidizing and includes a metal desirable in the refined metal to be recovered from the bath saturated with a metal oxide dispersed or dissolved therein whose metal also is desirable in the refined metal. The oxide is reduced to metal 40 by the transference of the oxygen thereof to combine with the omdizable impuritypf the bath (such as carbon). The impurity in the form of an oxide departs from the bath of metal being refined as a gas if gaseous, or into the slag if a solid. As the usual impurity is carbon, when oxidized it formscarbon monoxide and this, in being continually evolved, forms the atmosphere of the furnace. The reduced metal forms an addition to the metal content of the bath.
The cores 20 are composed of comminuted materials comprising those that are translatable under the conditions of temperature obtaining in the heated zone of the electrode, into a metal refining reagent. More particularly those mc.- 55
terials can be a metal oxide preferably as an ore; a reducing agent such as carbon in quantity insufficient to reduce all of the metal oxide so that the end product of the reactions in the electrode will be reduced metal and unreduced metal oxide; and a corrective for controlling the passage of the reactive materials through the heated zone of the electrode whereby the reduced metal yield ed therein is retained therein long enough to become superheated high enough above its melting point to become a solvent for the unreduced oxide but below the melting point of the oxide. A satisfactory degree of superheat is of the order of 600 'F. above the melting point of the metal. The result is the emission from the electrode of an oxidizing metal refining reagent. These reactions and the manner of attaining these results form the subject-matter of my patent application Ser. No. 59,690, filed January 18, 1936, (now Patent No. 2,070,186) and of its predecessor patent applications referred to therein, on which it depends for priority.
As the metal oxide is reduced to metal which first appears in the form of drops thereof, the reduced metal occupies less volume than the constituents which yield it. This causes the cores to become pitted or possessed of pores. The outer surface sections of the cores disintegrate slowly.
under the influence of the heat, although they 'hold the metal in place long enough to attain its desired superheat. As long as the cores are in core form, they exhibit a spon e-like function. Nevertheless, as the drops of metal form, they should be kept away from the carbon of the electrode and this is done to some extent by the sponge-like action of the core provided however,
the drop is not allowed to remain in too long contact with the carbon. Otherwise the metal will stick to the carbon and freeze the core against further forward progress thereof through the bore of the electrode. Such a prolonged contact of the core with one spot in the electrode tends to cause the oxide present in the core to give up some of its oxygen to the carbon of the electrode. Again, as the metal oxide usually used in this process is chromium oxide, or an ore containing it such as chromite, the reduced chromium being the heaviest constituent of the mass in the electrode tends to settle out and stratify therein whereas it is highly desirable to keep the molten or fiuid constituents in the electrode in well dispersed or mingled condition. And further, if the reduced metal such as chromium should stick to the electrode, the carbon thereof being hotter than the metal, will result in a detrimental pick up of carbon by the metal.
For overcoming or at least discouraging the encountering of these disadvantages, it is proposed herein to rotate the hollow electrodes. Rotation I thereof results in an action illustrated in Figs. 2 and 3. Herein is illustrated what happens to the cores as they are forced through the heated zone of the electrode so 20a represents a core 20 in one condition, 20b a core in a condition of partial disintegration, 200 a core in an advanced state of disintegration, and so on. The bore of the electrode is shown in dotted lines in order to show the decreased diameter and conical shape assumed by cores during their advance through the heated zone as a result of the joint causes of the reduction of some of the metal oxide of the core to metal and of the rotation of the electrode. The reaction between the reducing agent in the core and some of the metal oxide therein takes place under the influence Of the electrode.
temperature encountered by the cores in the heated zone of the electrode with the result that pores appear in the core and their size diminishes. Rotation of the electrode keeps the core and its contents free from the bore of the electrode because the core is caused to roll at a different rate than the speed of the inner wall of the electrode because the diameter of the core is less than that of the bore. The steady wear on the core and steady translation of its constituents discourages the core from breaking into fragments which would in turn cause jamming thereof in the bore. The space 22 existing be tween the core and the bore, that increases toward the arc end of the electrode, is useful and advantageous because it provides a ready escape for the carbon monoxide of the furnace that is constantly produced due to the oxidation of the carbon impurity of the metal being refined by the oxygen of the oxidizing refining reagent.
Satisfactory results have been attained by rotating the electrodes at a peripheral speed of three inches per minute, that is, one revolution of a ten inch diameter electrode in ten and a half minutes.
Thus, the step of rotating the electrode serves the several purposes of preventing the reduced metal and its oxide from remaining in fixed relationship with any particular spot in the bore of the electrode; of maintaining the fiuid constituents of the mass in the electrode in intermixed and intermingled condition; and of causing the cores to disintegrate gradually without breaking and thus avoid jamming thereof in the At the same time it assures the disintegration of the cores with the translation of their reactant materials to progress uniformly, dependably and in an orderly manner.-
I claim:
1. The steps in a process of refining metal material comprising passing into a substantially horizontal hollow electrode of an'electric furnace cores of a mixture capable of yielding metal and a metal oxide, meanwhile rotating the electrode.
2. The steps in a process of refining metal material comprising passing into an energized substantially horizontal hollow electrode of an electric furnace cores containing reactive materials capable of yielding in the heated zone of the electrode a superheated molten metal having a metal oxide dispersed therein, meanwhile rotating the electrode.
3. The steps in a process of refining metal material comprising supplying to the bore of an energized substantially horizontal hollow electrode of an electric furnace cores containing materials capable of being translated under the influence of heat into molten metal having a metal oxide dispersed therein, detaining the core materials in the heated zone of the electrode long enough for the molten metal to attain a temperature substantially above its melting point, meanwhile rotating the electrode whereby the cores disintegrate gradually into conical shapes as the core material thereof is translated.
4. The process of refining metal material comprising forming a molten bath of metal having an oxidizable impurity therein and an oxide containing slag thereon; passing into an energized substantially horizontal hollow electrode of an electric furnace cores containing materials capable of yielding in the heated zone of the electrode a molten metal having a metal oxide dispersed therein, meanwhile rotating the electrode, supplying the metal and oxide to the molten bath of metal in an atmosphere of carbon monoxide whereby there is effected an oxidation of the impurity of the bath with an increase of the metal content thereof and there is a departing of the resulting oxide from the molten metal, and then recovering the refined metal from the bath.
5. In the refining of a metal bearing material made up of a plurality of constituents including at least one metal as a desirable constituent thereof and at least one oxidizable undesirable constituent thereof, the process for modifying the proportion of certain constituents thereof which comprises forming a molten bath of the material to be refined and an oxidizing slag M thereon in a carbon monoxideatmosphere, forming an oxidizing reagent composed essentially of metallic oxide and a reduced metal at a temperature in excess of the melting point oi the reduced metal while conflned'in a substantially horizontal hollow electrode, meanwhile rotating the electrode, supplying a quantity of reagent to the bath for liquid admixture therewith under conditions for inducing an oxidizing action of the reagent upon the oxidizable undesirable constituent of the molten bath by virtue of which the proportion thereof is decreased through conversion into an oxide, and then recovering refined metallic material from the bath.
GILBERT E. SEIL.
US113096A 1936-11-28 1936-11-28 Electric furnace process Expired - Lifetime US2104530A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US113096A US2104530A (en) 1936-11-28 1936-11-28 Electric furnace process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US113096A US2104530A (en) 1936-11-28 1936-11-28 Electric furnace process

Publications (1)

Publication Number Publication Date
US2104530A true US2104530A (en) 1938-01-04

Family

ID=22347563

Family Applications (1)

Application Number Title Priority Date Filing Date
US113096A Expired - Lifetime US2104530A (en) 1936-11-28 1936-11-28 Electric furnace process

Country Status (1)

Country Link
US (1) US2104530A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2464008A (en) * 1945-10-10 1949-03-08 Commerce Pattern Foundry & Mac Continuous replenishment of electrodes in electric salt bath structures
US3010796A (en) * 1959-01-12 1961-11-28 Monsanto Chemicals Electric furnace operation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2464008A (en) * 1945-10-10 1949-03-08 Commerce Pattern Foundry & Mac Continuous replenishment of electrodes in electric salt bath structures
US3010796A (en) * 1959-01-12 1961-11-28 Monsanto Chemicals Electric furnace operation

Similar Documents

Publication Publication Date Title
US3005246A (en) Method of producing high-quality ingots of reactive metals
US2446637A (en) Method for melting brass chips
US4133517A (en) Continuous reflux refining of metals
US2104530A (en) Electric furnace process
US3746533A (en) Process of producing ferro-nickel in a rotary furnace including pelletizing and pre-reducing ore
SU1128844A3 (en) Method of obtaining blister copper from copper ore
US2403419A (en) Method of recovering the constituents of scrap bi-metal
NO128620B (en)
US3091525A (en) Deoxidation of refractory metal
JPH0873906A (en) Method for producing titanium powder
US2805148A (en) Method of melting refractory metals
US2320206A (en) Reaction method
US2226967A (en) Production of stainless steels
US3317308A (en) Process for reduction of iron ores
US3077396A (en) Method of feni alloy production from nickel bearing iron ores
US1542784A (en) Refractory crucible
JPS58130232A (en) Method of refining high strength lead
US2240231A (en) Production of alloys of chromium
US807271A (en) Process of extracting metals from their sulfids.
US2387014A (en) Rotary kiln
US2182129A (en) Metallurgy
US2084978A (en) Refining alloys
US3001863A (en) Process for obtaining ferrous metals and alloys from their ores
USRE18930E (en) Refining i
US2237867A (en) Method of making sponge iron powder