US3326671A - Direct smelting of metallic ores - Google Patents

Direct smelting of metallic ores Download PDF

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Publication number
US3326671A
US3326671A US570270A US57027066A US3326671A US 3326671 A US3326671 A US 3326671A US 570270 A US570270 A US 570270A US 57027066 A US57027066 A US 57027066A US 3326671 A US3326671 A US 3326671A
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United States
Prior art keywords
zone
slag
furnace
smelting
molten material
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US570270A
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Howard K Worner
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Individual
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Individual
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Priority claimed from AU27676/63A external-priority patent/AU273494B2/en
Priority to GB6523/64A priority Critical patent/GB1003026A/en
Priority to SE2015/64A priority patent/SE304581B/xx
Priority to US345987A priority patent/US3288451A/en
Priority to DE19641519752 priority patent/DE1519752A1/en
Priority to FR964764A priority patent/FR1387509A/en
Priority to BE644174D priority patent/BE644174A/xx
Priority to DE1964F0042480 priority patent/DE1294022B/en
Priority to AT309464A priority patent/AT266461B/en
Priority to GB14818/64A priority patent/GB1055935A/en
Priority to BE646429A priority patent/BE646429A/xx
Priority to NL6403867A priority patent/NL6403867A/xx
Priority to SE4457/64A priority patent/SE315741B/xx
Priority to FI640758A priority patent/FI43791C/en
Priority to YU498/64A priority patent/YU31189B/en
Priority to FR970642A priority patent/FR1429265A/en
Priority to LU45859D priority patent/LU45859A1/xx
Priority to US390042A priority patent/US3326672A/en
Priority to DE19641458306 priority patent/DE1458306B2/en
Priority to GB34235/64A priority patent/GB1064826A/en
Priority to FR986427A priority patent/FR1405775A/en
Priority to BE652436D priority patent/BE652436A/xx
Application filed by Individual filed Critical Individual
Priority to US620568A priority patent/US3432157A/en
Priority to US619108A priority patent/US3463472A/en
Publication of US3326671A publication Critical patent/US3326671A/en
Application granted granted Critical
Priority to MY197089A priority patent/MY7000089A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/04Obtaining zinc by distilling
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B5/00Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
    • C03B5/04Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in tank furnaces
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B5/00Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
    • C03B5/12Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in shaft furnaces
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B13/00Making spongy iron or liquid steel, by direct processes
    • C21B13/10Making spongy iron or liquid steel, by direct processes in hearth-type furnaces
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B13/00Obtaining lead
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/02Obtaining nickel or cobalt by dry processes
    • C22B23/025Obtaining nickel or cobalt by dry processes with formation of a matte or by matte refining or converting into nickel or cobalt, e.g. by the Oxford process
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B25/00Obtaining tin
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B5/00General methods of reducing to metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B9/00General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
    • 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
    • Y02P10/10Reduction of greenhouse gas [GHG] emissions
    • Y02P10/134Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen
    • 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
    • Y10S75/957Continuous refining of molten iron

Definitions

  • ABSTRACT OF THE DISCLOSURE A method for continuously producing metals from ore and concentrate base material by providing in a furnace chamber intercommunicating smelting, refining and slag separation zones having molten material therein.
  • the base material is fed to the molten material in the smelting zone as the molten material continuously flows from the smelting zone to the refining zone from where metal is withdrawn while the slag produced flows into the separating zone from where it is withdrawn.
  • Oxygen containing gas is introduced into the molten material during its passage through the furnace chamber.
  • This invention relates to the direct smelting of metallic ores and concentrates, and refers particularly to a method for the production of metals directly from particulate ores and concentrates and to apparatus for car rying out such method.
  • the term metal in this Specification includes metals, alloys and other metal-nich prod-ucts of the smelting operation.
  • the invention is applicable to the smelting of ores or concentrates (e.g. sulphide ores or. concentrates) of metals such as copper, nickel and lead, and to the production of iron and steel from oxide ores or concentrates of iron. It is also applicable to the smelting of zinc bearing ores and concentrates, subject to the considerations referred to subsequently in this specification.
  • the invention can, with the appropriate modifications hereinafter described, be usedfor smelting ores or concentrates a proportion of which is in lump form or all or a pro portion of which comprises pelletisedor otherwise agglomerated fines.
  • particulate in this specification refers to and includes solid materials of the abovementioned types, the particles of which are fineenough to be handled in tubes pneumatically or 'by gravity flow. In most cases the particles are smaller than one centimetre in diameter.
  • ores includes ores, or concentrates of ores, in any form including pelletized form, and in the case of iron prereduced material in any form.
  • the invention makes use of the fast reactions between oxygen-containing gas, such as air, oxygen or oxygenenriched air, and hot particulate oxidisable solid materials such as sulphides or solid"carbonaceous fuels.
  • oxygen-containing gas such as air, oxygen or oxygenenriched air
  • hot particulate oxidisable solid materials such as sulphides or solid"carbonaceous fuels.
  • the heat generated by these fast reactions provides the energy necessary to keep the melting'and smelting operations going.
  • the invention may therefore be described as autogenous melting and/ or smelting. It differs from other autogenous smelting operations, in part, in that it involves reactions under or in proximity to' the surface of a flowing stream ofmoltenmaterial, such reactions being induced by injecting or feeding particulate reactants and an oxygencontaining gas onto or under the surface of the aforementioned flowing stream.
  • the movement of the flowing stream of molten ma- See terial may be induced by the design of the furnace, by the angles of impingement on the molten material of the particulate raw materials and/ or of the injected gases, or by the introduction into the furnace of an initiator stream of molten material from an auxiliary furnace or smelter, or by a combination of two or more of these factors.
  • the auxiliary furnace (if employed) may be contiguous with or separate from the furnace of this invention and may be of any suitable type, and'the flow of molten material therefrom may be reduced or discontinued when the smelting operation in the furnace of this invention has been stabilized.
  • the invention in one general form is a method of producing metals directly from particulate ores and concentrates which comprises the steps of: preparing in a furnace chamber a bath of molten material from the particulate ores or concentrates and/or from the products of a previous melting or smelting operation; maintaining in the furnace a feed and primary smelting zone, a refining zone and a slag settling zone; causing the molten material to flow in a stream continuously through the chamber and away from the feed and primary smelting zone; feeding the ores or concentrates in particulate form into or onto the stream of molten material in the feed and primary smelting zone; introducing an oxygen-containing gas into or onto the stream of molten material during its passage through the furnace chamber; developing an exothermic reaction with the bath of molten material between the oxygen-containing gas and at least one component of the molten material; withdrawing slag from the slag settling zone; withdrawing molten material from the refining zone; and withdrawing
  • the invention in another general form is a method of producing metals directly from particulate ores or concentrates which comprises the steps .of: preparing in a furnace chamber a bath of molten material from the particulate ores or concentrates and/or from the prod ucts of a previous melting or smelting operation; maintaining in the furnace chamber a feed and primary smelting zone; a secondary smelting zone, a slag settling zone, and a refining zone; causing the molten material to flow in a stream continuously through the chamber from the feed and primary smelting zone to the secondary smelting zone and to the refining zone; causing slag formed on the surface of the molten material to flow to the slag settling zone; feeding the particulate ores or concentrates into or onto the stream of molten material in the feed and primary smelting zone; introducing an oxygen-containing gas into or onto the stream of molten material at two or more points therealong; developing an exothermic
  • the invention in another general form is apparatus for carrying out the abovementioned method, comprising: a furnace having a substantially enclosed chamber in which is maintained a continuously flowing stream of molten material, means for feeding particulate ores or concentrates into or onto the stream of molten material, means for introducing oxygen-containing gas into or onto the stream of molten material, means for withdrawing slag from the furnace at one point, means for withdrawing molten metal from the furnace at another point, and
  • lance in this specification includes a tube raving one or more discharge outlets through which pariculate material and/ or oxygen-containing gas, such as .ir, oxygen or oxygen-enriched air, and/ or gaseous, liquid If particulate solid fuel and/ or fluxes or other additives, s or are injected or fed into the furnace.
  • pariculate material and/ or oxygen-containing gas such as .ir, oxygen or oxygen-enriched air, and/ or gaseous, liquid
  • the refractories used to line the furnace are appro wriate to the reactants used and products formed in the urnace and to the temperature and other conditions exsting in the furnace.
  • fluid-cooled jackets may be used to form the walls and/or roof of the furnace.
  • the furnace of this invention when viewed in plan may )e linear, annular, rectangular, D-shaped, U-shaped or )f other suitable shape, including the forms of the invenion illustrated in the accompanying drawings.
  • annular furnace refers :o a furnace whether circular or otherwise in which one )r more continuous circuits is provided for the fiow of molten material, and in which portion of the molten naterial is caused to recycle from the refining zone into ;he feed and primary smelting zone.
  • the invention includes, but is not limited to, the use of an annular furnace.
  • the slag settling zone and the refining zone of the furnace may comprise branches or extensions to the furnace which connect with the smelting zone or zones, and in one form of the invention the slag settling zone is disposed to connect with the stream of molten material before the latter reaches the refining zone.
  • the gas ofitake is conveniently located above the slag settling zone or branch.
  • the particulate raw materials (which are preferably preheated) are jetted or fed into or onto the molten material in the furnace at the feed and primary smelting zone. These materials may be fed by screw feeders, pneumatic injection or other means. Oxygen-containing gas is preferably introduced with the particulate materials, and may also be introduced into the furnace at other positions so as to impinge onto or into the flowing stream of molten material.
  • the heat developed within the bath of molten material by exothermic reactions may be supplemented by the burning of particulate materials in transit to the bath and/or by burning of combustible gases generated by reactions within the bath and/or by combustion of carbonaceous fuel added with the particulate raw materials.
  • the invention makes use of modern techniques for dispensing and injecting powders along with air or air enriched with oxygen or other gas. In some cases a proportion of the particulate materials and any lump materials may be fed into the bath under gravity or introduced by screw feeders.
  • the invention takes advantage of the speed of reaction between hot fine particulate sulphides on the one hand or finely particulate coal or the like on the other, and hot oxygen-containing gases. As soon as the particulate materials enter the hot furnace and certainly when they strike or enter the molten bath they react vigorously.
  • Means such as a gas barrier may be provided in the furnace above the stream of molten material to substantially prevent reverse flow of gases.
  • the slag settling zone or branch is preferably constructed with a ridge or slag overflow region and with the floor of said zone or branch sloping upwardly from the furnace chamber to the ridge or slag overflow region.
  • the end of the floor of the slag zone or branch adjacent to the smelting chamber of the furnace is preferably located at or near the intended level of the matte or metal in the said chamber, and the level of the ridge or slag overflow is preferably located above the intended level of the matte or metal.
  • the conditions in the slag settling zone, and in the lower region of the exit end of the refining zone from which the metal is tapped, are preferably quiescent. Gases may be caused to impinge into or onto the surface of the material in the refining zone, or a portion thereof, in such a manner as to create a countercurrent flow of slag in the refining zone, on the surface of the molten metal or matte, away from the metal outlet.
  • FIGURE 1 is -a view in sectional plan of one form of furnace
  • FIGURE 2 is a view in sectional elevation on the line 2-2 of FIGURE 1;
  • FIGURE 3 is a view in section on the line 33 of FIGURE 1;
  • FIGURE 4 is a view in sectional plan of another form of furnace
  • FIGURE 5 is a view in sectional elevation on the line 55 of FIGURE 4;
  • FIGURE 6 is a view in section on the line 6-6 of FIGURE 4;
  • FIGURE 7 is a view in sectional plan of a further form of furnace
  • FIGURE 8 is a view in sectional elevation on the line 8-8 of FIGURE 7;
  • FIGURE 9 is a perspective view of a further form of furnace.
  • FIGURE 10 is a view in sectional plan of the furnace shown in FIGURE 9;
  • FIGURE 11 is a view in sectional elevation on the line 11-11 of FIGURE 10;
  • FIGURE 12 is a view in sectional plan of a further form of furnace
  • FIGURE 13 is a view in sectional elevation on the line 13-13 of FIGURE 12;
  • FIGURE 14 is a perspective view of a further form of furnace
  • FIGURE 15 is a view in sectional plan of the furnace shown in FIGURE 14;
  • FIGURE 16 is a view in sectional elevation on the line 1616 of FIGURE 15;
  • FIGURE 17 is a view in sectional elevation on the line 1717 of FIGURE 15;
  • FIGURE 18 is a view in sectional plan of a further form of furnace
  • FIGURE 19 is a view in sectional elevation on the line 1919 of FIGURE 18.
  • FIGURE is a view in sectional elevation on the line 2020 of FIGURE 18;
  • FIGURE 21 is a sectional plan view of a substantially U-shaped furnace constructed in accordance with the invention.
  • FIGURE 22 is a view in sectional elevation on the line 22-22 of FIGURE 21;
  • FIGURE 23 is a view in sectional elevation on the line 23-23 of FIGURE 21;
  • FIGURE 24 is a view in sectional elevation on the line 24-24 of FIGURE 21;
  • FIGURE 25 is an isometric view of apparatus for the treatment of ores or concentrates, particularly of iron oxide ores or concentrates, according to the invention.
  • FIGURE 26 is a sectional plan view of the furnace shown in FIGURE 25;
  • FIGURE 27 is a view in sectional elevation of the furnace shown in FIGURE 25
  • FIGURE 28 is a sectional plan view of a modified form of furnace;
  • FIGURE 29' is a view in sectional elevation taken on the line 2929 of FIGURE 26;
  • FIGURE 30 is a view in sectional elevation of a modified ore feed arrangement
  • FIGURE 31 is a perspective view of a device for feeding and'pre-heating particulate ores or concentrates.
  • the furnace shown in these figures is of the annular type and comprises an external cricular wall 30, an internal circular wall 31, a floor 32, and annular chamber 33, and a domed annular roof 34.
  • a slag settling branch 35 and a refining branch 36 are connected to the annular chamber 33.
  • a gas oiftake 37 is provided above the slag settling branch 35.
  • Particulate ores or concentrates preferably preheated, and where necessary preblended with carbonaceous fuel, are fed pneumatically. or by other means into the annular chamber through lances or powder feeders 38, 39 which project through the roof 34 or through the external wall 30.
  • a bath of molten material 40 is formed in the bottom or trough of the chamber 33 and is caused to fiow generally in an anti-clockwise direction as shown in FIGURE 1.
  • the direction of flow of metal or matte is shown by arrows in full lines and the direction of flow of slag is shown by arrows in dotted lines.
  • the particulate ores or concentrates are fed into or onto the molten material 40 in the feed and primary smelting zone A.
  • Oxygen-containing gas is injected into or onto the molten material 40 through lances 41, 42 which project into the secondary smelting zone B, and also through lances 43, 44, which project into the refining zone D within the refining branch 36, and if desired oxygencontaining gas may also be injected with the particulate material through lances 38, 33.
  • the lances 38, 39, 41, 42, 43, 44 and 45- are shown in the drawings to terminate a short distance above the surface of the molten material 40 so that the particulate materials and/or gases injected therethrough are directed onto the surface of the molten material, but in an alternative form of the invention (not shown) any of the lances vmay be designed and arranged to project beneath the surface of the molten material.
  • All orsome of the lances 3 8, 39, 41 and 42 may be tilted 0r inclined at an angle to the vertical in order to impart or to assist in imparting forward movement to the molten material 40 in the required direction in the chamber 33 (anti-clockwise in the drawing).
  • the lances 43, 44, 45 are inclined in the reverse'direction to that of the flow of metal or matte in the refining branch 36, so as to create a countercurrent flow of slag in the re- .fining branch 36 away from the taphole 46 and towards the annular chamber 33.
  • the metal or matte flows outwardly in the refining branch 36 and is discharged through taphole or outlet 46.
  • the slag branch 35 is provided with an outwardly and upwardly sloping floor 47, a ridge or slag overflow 48, a slag pool or reservoir 49 and a slag settling zone C.
  • a gas barrier 51 may be provided in the annular chamber 33 to extend from the roof 34 almost to the surface of the molten material 40.
  • the process achieves the continuation of the oxidation of sulphur, iron and some other readily oxidisable elements commenced in the feed zone A.
  • the sulphur leaves the bath as S0 while the iron and other oxidisable elements enter the slag by a reaction of the type
  • the oxygen-containing gas blown in at positions such as 41 and 42 serves to combust any unburnt carbon or carbon monoxide leaving the feed zone A and entering the secondary smelting zone B.
  • the oxygen-containing gas blown in at positions such as 43, 44, 45 serves to oxidise out the carbon from the semi-steel bath to bring it to the desired value before steel is tapped through taphole 46.
  • Slag formed in the feed and primary smelting zone A and secondary smelting zone B flows slowly and quiescently out through the slag branch 35, over the ridge or overflow 48 and is discharged through taphole 50.
  • the slag in the slag branch 35 is kept liquid by heat exchange (from the'hot gases moving'to the gas ofitake, 37).
  • the metal or matte continues to flow around the annulus and a proportion enters the refining branch 36, where it is withdrawn continuously or semi-continuously through taphole 46. Any slag which forms in the refining branch 36 is caused to flow countercurrently back into the annular chamber 33 and portion of it may be recycled and portion may flow countercurrent to the matte or metal and leaves the furnace at 50.
  • Gases generated by lancing at positions such as 38, 39', '41, 42 tend to move concurrently with the molten material, whereas gases generated by lancing at positions such as 43, 44, 45 may tend to move countercurrent to the molten material, at least in portion of the annulus.
  • the proportion of the molten material which is recycled into the feed and primary smelting zone A is not critical and is determined mainly by the relative rate of feed of solids to the rate of tapping of slag through taphole 50 and of metal through taphole .46.
  • ing pool of molten material may be built up from either concentrates plus flux, and/or from the products of a previous run.
  • more finely particulate flux can appropriately be added through one or more of the lances in the refining branch 36 such as, for example, throughlance 45. Alternatively itmay be added in a position near to lance 45 through ports or side doors (not shown).
  • the slag generated by the reaction of this flux addition tends to move countercurrent to the matte or metal. In the smelting or sulphides this assists in the removal of the last traces of unwanted elements, for example, iron in the case of copper and nickel, and in the case of steelmaking, the countercurrent slag.
  • the floor of the refining branch 36 may be more or :ss horizontal in the case of iron and steelmaking. In he case of smelting of sulphides, however, it is often .n advantage for the said floor to slope gently downwards mm the main furnace floor towards the taphole 46 as hown at 36' in FIGURES 11, 13 and 16. -In the case If both copper and lead production, it is advantageous have at the end of the refining branch 36, a sump l6 (such as that shown in FIGURE 13) which is prefrably substantially deeper than the rest of the bath of he refining branch 36. The submerged taphole 46 or .yphon can appropriately be connected to the bottom of his sump 46'.
  • the metal in the bottom of the :ump 46 is cooled to within about 80 C. to 150 C. at its melting point before it passes out through the subnerged taphole or syphon. This is to cause as much as Jossible of the contained sulphur to come out of soluion in the metal before the metal leaves the furnace.
  • the cooling may be achieved by use of a deep sump or )y cooling fluid passing through metal coolers -or by slowing cold air through a lance or lances deeply submerged in the sump or by other suitable means.
  • lump materials as for example cement copper in the case of copper smeltlng
  • these materials can be added through ports or doors (not shown) in the walls or roof of either the annulus portion of the furnace or of the refining branch 36.
  • the sensible heat in the exit gases may be used for a number of purposes, such as drying and preheating the particulate feed materials, preheating the oxygen-containing gases, for steam raising or for other purposes.
  • some of the gas, utilized with fine coal or char may also be used for partial pre-reducing of the particulate ores before feeding to the furnace.
  • a drain plug In order to drain the furnace at the end of a campaign or run a drain plug can be provided at a convenient position; alternatively the whole furnace may be designed to permit slight tilting towards the taphole 46.
  • FIGURES 4, and 6 a furnace of rectangular shape is shown.
  • the references have the same connotations as in FIGURES 1, 2 and 3.
  • the furnace has an outer wall 30 and an internal island wall 55.
  • the lances 41 and 42 enter the furnace through the side wall 56 and are disposed at an angle as shown in FIGURE 4 in order to impart forward movement to the molten material which flows from the feed and primary smelting zone A towards the secondary smelting zone B and then continues its anticlockwise movement within the furnace.
  • the gas space 57 above the molten material to the left of the island wall 55 is considerably greater than the gas space 58 on the feed zone side of the wall 55. This has the advantage that the gas flow rate is lowered in the 8 larger space 57 thus enabling entrained particulate materials and slag droplets to fall back into the bath before the gases pass out through the slag branch 35 and gas olftake 37.
  • the slowing down of the gases in this space 57 also facilitates the burning of the carbon monoxide leaving the feed zone A. It is advantageous in this particular application to blow the oxygen-containing gas'through turbulant jets at positions such as 41 and 42. This assists the complete combustion of carbon monoxide and of fine entrained char or coke particles.
  • FIGURES 7 and 8 a furnace is shown having two island walls 55 and 55', two feed and primary smelting zones A and A, and two sets of lances 38, 3-? and 38' and 39', through which particulate materials may be in troduced either concurrently or alternately into the feed zones A and A respectively. Lances 41 and 41' inclined in opposite directions, are provided for injection of oxygen-containing gas. In this furnace the slag branch 35 is disposed opposite to the refining branch 36. p
  • a refractory barrier (not shown) is lowered through removable portions of the roof 34 of the furnace at positions at the ends of the island wall 55 and 55' as the case may be.
  • FIGURES 9, 10 and 11 a linear furnace is shown having a central feed and primary smelting zone A into which particulate raw materials and (if desired) oxygencontaining gas, are injected through inclined lances 38, 39. These lances are arranged approximately tangentially to the feed zone A, so as to impart a circulatory or rotary movement to the molten material in said zone.
  • the chamber is narrowed on either side of said zone A as shown at 62 and 63 in FIGURE 10, thereby providing an approximately circular feed zone in which the said circulatory movement of the molten materials is facilitated.
  • the slag branch 35 and the refining branch 36 are disposed on opposite sides of and are connected to the central feed zone A as shown in FIGURE 10.
  • the furnace may be tilted through a slight angle on rollers 59 to facilitate fettling of refractories and/ or draining of liquids at the end of a campaign.
  • a stationary chimney is provided over the gas oiftake aperture 37 at the end of the furnace.
  • FIGURES 12 and 13 a further modified form of furnace is shown having a circular feed smelter zone A into which particulate materials and (if desired) oxygencontaining gas are injected through lances 38, 39 which are angled so as to impart circulatory movement to the molten material in zone A.
  • the slag branch 35 extends laterally at right angles to the refining branch 36.
  • the branch leading to the secondary smelting zone B, slag settling zone C and refining zone D which are arranged in a straight line in said branch, extends tangentially from and connects with the feed and primary smelter zone A. Circulation is imparted to the molten material in the feed zone A, preferably in a direction which directs such material along the tangential branch to the secondary smelting zone B and hence to zones C and D.
  • the branch may be narrowed between zones C and D.
  • two circulatory feed zones may be provided in which circulation of molten material is effected in opposite directions, and the said branch leading to zones B, C and D is connected cen trally to the chamber containing the two circulatory feed zones.
  • FIGURES 14 to 17 a U-shaped furnace is shown in which the slag branch I 35 and refining branch 36 are parallel and side-by-side.
  • Particulate feed materials are injected through either or both lances 38, 39.
  • Oxygen-containing gas is injected through lances 41, 42 and lances 43, 44, 45.
  • Particulate materials and/or oxygen-containing gas may be fed together or separately through lances 38, 39 as desired.
  • a conical or domed roof (not shown) may be provided over the circulatory feed zone A and the said roof may be of good quality refractory or may be fluid cooled metal.
  • a gas otftake chimney 37 is provided at the end of the slag branch 35.
  • annular furnace which is provided with a central core 60 of lump ore or concentrates or agglomerated or pelletised fines.
  • the pelletised ore or the like is fed through chute 75 into a rotary kiln 76, heat exchange being effected to the incoming pelletised ore from the exit gases passing up stack 70.
  • the residence time in the kiln 76 is sufiicient to enable some pre-oxidation or pre-reduction (as the case may be) of the pelletised ore or concentrate to be effected before the material is discharged into the vertical shaft 61 and thence into the centre of the furnace.
  • Further particulate ore or concentrate may be charged to the feed-smelter zone A of the furnace by means of hoppers 77 and screw feeders 78, 79.
  • Oxygen-containing gas is introduced through lances 41, 42, 43, 44 and 45.
  • Other features of the furnace are similar to those of the furnace shown in FIGURES l to 3.
  • the pellets may be formed with or without binding agents and with or without fluxes incorporated.
  • the carbon monoxide-rich gases passing up shaft 61 to the kiln are too hot, they may appropriately be cooled by injecting steam in through a lance or port (not shown). Such steam, apart from its cooling effect, enters into a gas shift reaction with the very hot carbon monoxide thus:
  • the hot hydrogen thus produced acts as a highly efficient reductant in the kiln 76.
  • the furnace shown in FIGURES 21 to 24 is particularly useful for the direct smelting of copper sulphide concentrates by the process of the invention and this embodiment of the invention,
  • Warm dry copper sulphide concentrates are introduced in particulate form into the feed and smelting zone A through lance 38 which in this embodiment is arranged concentrically within an outer tube 91, air and sometimes air plus a little oil being blown under pressure through the annular space between the lance 38 and tube 91. Siliceous flux may be added with the concentrates.
  • the feed material is preferably preheated (e.g. to a temperature of between 200 C. and 650 C.) prior to or during its introduction into the furnace.
  • the concentrates are injected into the bath of molten material 40 in the smelting zone A in such .a manner as to cause turbulence and agitation of the molten material.
  • the lance 38 is arranged at an angle of between about 40 to about 80 to the horizontal as shown in FIG URE 22 so as to cause the concentrates to impinge at an angle onto the surface of the molten material 40 in zone A.
  • the lance 38 is disposed approximately tangentially to the circular smelting zone A so as to cause circulation of the molten material in the said zone in the direction shown by the arrows 92 in FIGURE 21.
  • the direction of circulation of the molten material 40 in zone A is such that slag flowing from the refiner zone D to the slag separation zone C travels by the longest route through zone A so that it has a maximum residence time in zone A.
  • the floor 93 of zone A of the furnace is substantially horizontal.
  • the refiner branch D of the furnace is of elongated rectangular shape in plan and its floor 94 slopes downwardly from the junction of zone D with zone A to a V-shaped passage or sump 95 formed in the end wall 83 through which molten copper 97 flows from the refiner zone D.
  • the angle of slope of the floor 94 is between 3 and 30", preferably between 5 and 10.
  • the lower end 96 of the end wall 83 projects downwardly below the level of copper 97 in the refiner zone D.
  • the sump 95 communicates with a metal reservoir 98 formed in furnace extension 99.
  • a copper tapho le 46 communicates with the metal reservoir 98 below the slag level in the refiner zone D and preferably at approximately the same level as that of the matte-white metal complex 100 in the refiner branch D.
  • Silica or siliceous ore flux is added mechanically or pneumatically through ports 102 in the internal wall 84.
  • the ports 102 are disposed more or less directly opposite to the lances 43, 44, 45 so that the silicious' material delivered from the ports 102 serves to protect the refractory of the wall 84 from erosion due to splashing of molten material caused by air injection through the said lances.
  • a main gas offtake 37 for sulphur dioxide bearing furnace gases is provided above the exit end of the refiner zone D.
  • a port 103 is provided in the roof 86 through 1 l vhich lump concentrates or lump ore may be added to he molten material in the refiner zone D.
  • the slag separation zone C of the furnace is provided vith a slag weir 48 which may be air-cooled, a slag pool )r well 4-9, a matte taphole 104 through which matte 105 nay be tapped at infrequent intervals as required, a slag aphole 50, and an auxiliary gas oiftake 106.
  • the floor 47 )f the slag separation zone C slopes gently upwards from he smelting zone A to the slag weir 48.
  • a port 107 is )rovided in the roof 86 through which a reducing agent, L1Ch as iron sulphide, in the form of pyrites, pyrrhotite r low grade copper sulphide concentrates, and/or a caraonaceous fuel, may be added to the molten material in the ;lag separation zone C.
  • a reducing agent L1Ch as iron sulphide, in the form of pyrites, pyrrhotite r low grade copper sulphide concentrates, and/or a caraonaceous fuel
  • An oil burner 108 projects through the wall 80 into the smelting zone A and its flame is directed onto the surface of the molten material 40 therein; an oil burner 109 projects into the furnace extension 99 and its flame which is preferably oxidising is directed onto the surface of the molten copper in the copper reservoir 98, and products of combustion enter the furnace proper through port 109a; and oil burner 110 projects through the side wall 81 and its flame, which is preferably reducing, is directed onto the surface of the slag in the slag separation zone C; and an oil burner 111 projects through the end wall 83 and its flame, which is preferably reducing, is directed onto the surface of the slag in the slag pool 49.
  • the oil burner 110 is directed transversely of the general direction of the flow of the slag through the slag separation zone C soas to impart a gentle circulation or eddying motion to the slag in the zone C as indicated by the arrows 112 in FIGURE 21.
  • the oil burner 111 is directed onto the slag in the slag pool 49 so as to cause a gentle circulation of the said slag as shown by the arrows 113 in FIGURE 21.
  • the circulation of slag indicated at 112, 113 is substantially confined to the surface layers of the said slag and is not such as to disturb the generally quiescent conditions prevailing in the slag separation zone C and slag pool 49.
  • the said circulation of slag is such as to increase the residence time of the slag in the slag separation zone C and the slag pool 49 and thus provide greater opportunity for the elimination of copper from the slag by settling out of fine prills of metal or matte.
  • Inspection and sampling ports 114 and 115 are formed in the end wall 82 and side wall 81 respectively, and are closed by refractory plugs 116, 117 respectively.
  • Port 115 is a convenient entry point for the addition to the bath of a reducing agent, such as a carbonaceous fuel, e.g. coal.
  • Matte generated in the smelting zone A being heavier than the slag, settles towards the floor of the furnace and then as it becomes heavier by the progressive elimination of sulphur and iron it gravitates down the sloping floor of the refiner branch D towards the sump 95.
  • Air under pressure is blown through the lances 43, 44, 45 into the molten material in the refiner branch D so as to create vigorous turbulence in the said material and to effect the progressive oxidation of sulphur and iron in the matte in said zone D.
  • Siliceous flux in the form of silica sand or finely crushed copper ore is added through ports 102.
  • the sulphur dioxide formed by oxidation of the sulphur enters the furnace gases which are withdrawn through gas oiftake.
  • the iron oxide formed in zone D reacts with the silica to form slag.
  • Lump copper sulphide concentrates are added through port 103, for the purpose of minimizing the formation of magnetite in the upper layers of the slag in the zone B.
  • the slag 101 formed in zone D rises to the surface of the matte and as it accumulates on the surface of said matte it flows towards the smelting zone A countercurrently to the flow of matte in zone D.
  • Copper 97 formed by oxidation of the white metal in the matte-white metal complex 100 in zone D settles out in the lower part of the zone D and flows through the sump 95 into the metal reservoir 98 from which it is tapped at taphole 46-.
  • An oxidising flame from burner 109 may be directed onto the surface of the copper in reservoir 98 in order tooxidise residual sulphur. Alternatively, the sulphur may be removed in a separate furnace.
  • the slag flowing countercurrently in the refiner zone D flows through the smelting zone A in the general direction of the circulation of material in zone A, that is, mainly adjacent to the outer wall of zone A, its residence time in zone A being thereby increased.
  • zone A the freshly melted concentrates, now substantially in the form of droplets of matte, are agitated with and dispersed into the said slag. This has the effect of stripping of a substantial proportion of copper in the slag stream passing through zone A.
  • the slag then flows from zone A into the relatively quiescent slag separation zone C, passing through the restricted portions 90a, 90b, of zone C into the larger portion 900 of said zone.
  • a convenient manner of maintaining such reducing conditions in the slag separation zone C is by the addition of pyrites or another source of iron sulphide :and/or by the addition of a reducing agent and/or by having a gentle jet of a reducing flame (such as, for example, from burner 110) directed at a relatively low angle over the slag so that gentle circulation is achieved and the iron sulphide and/or reducing agent is distributed and dispersed over the slag surface.
  • a gentle jet of a reducing flame such as, for example, from burner 110
  • the gentle circulation induced in the slag separation zone C increases the residence time of the top layers of slag in that zone and thus provides greater opportunity for matte particles to settle alnd thus decrease the amount of copper tapped in the s ag.
  • Another manner of creating reducing conditions in the slag separation zone C is by prilling iron sulphide with oil so that when the oiled pyrites is added to the slag separation zone C the oil burns with a reducing flame at the slag surface. This also promotes the melting and incorporation into the slag of iron sulphide which itself acts as a reducing agent.
  • Matte which settles out from the slag in the slag separation zone C flows down the sloping floor 47 of said zone C towards the smelting zone A in a direction countercurrent to the general flow of slag through the zone C.
  • the slag after separation of matter and stripping of copper in zone C, flows over the slag weir 48 into the slag pool 49 where fin-al separation of matte and copper therefrom is effected.
  • Burner 111 is operated to raise the temperature of the slag in pool 49, to impart a gentle circulation of said slag in the pool 49 to ensure maximum matte 13 separation, and, being a reducing flame, to minimize magnetite formation in the slag.
  • Slag is tapped through slag taphole 50.
  • the numeral 120 represents a disc pelletiser in which composite pellets P are produced from oxide ores or concentrates, carbonaceous material and a binder.
  • the pellets P are fed from pan feeder 121 into one end of a rotary metallisin g kiln 122.
  • air is admitted at pipe 125 and products of combustion are removed through stack 126.
  • the rotary kiln 122 delivers the metallised pellets into a column 123 which is mounted vertically over the smelting zone A of the furnace F, preferably to one side of said zone A.
  • the pellets fall by gravity in the column 123 into the circulating and turbulent bath of molten material in the said smelting zone.
  • Air or steam, or both, may be admitted to column 123 through heat resitsant retractable pipes 127a and 127b. Gases may be withdrawn through gas offtake 141a, which is controlled by a slide valve 145.
  • a similar control valve (not shown) may be provided on stack 126.
  • the furnace F is provided with a substantially circular smelting zone A and with an elongated refining zone D and a sla-g separation zone C which are connected to the smelting zone A by restricted openings or passages a and b respectively.
  • the furnace F is of U-shape, the refining zone D and slag separation zone C being arranged parallel to one another and separated by wall 131, but it will be understood that furnaces of other shapes may be employed.
  • Lances 128a and 128b project through the wall of the furnace F into the smelting zone A, and are inclined downwardly and are also arranged substantially tangentially to the zone A. Air and/or particulate carbonaceous material may be injected into the bath in zone A through lances 128a and 128b. A burner 129 also projects tangentially into the smelting zone A. Apertures 142, 142' are provided in the roof of the furnace F through which fine lump basic refractories, e.g.
  • dolomite, or other materials may be added to the bath, the apertures 142 being located above the smelting zone A and the aperture 142' being located above the slag separation zone C.”
  • Coke or other slag conditioning agents may be added to the slag separation zone through aperture 143.
  • Lances 132, 133, 134 pr-oject (if desired at an incline) into the refining zone D, and oxygen-containing gas is injected through the said lances into the turbulent molten material in the zone D.
  • the lances 132, 133, 134 preferably incline downwandly and towards zone A.
  • Metal is withdrawn from-the refining zone D at taphole 139 and underneath slag baffle 140.
  • a slag weir 137 is provided in the slag separation zone C over which slag overflows-into a slag pool 144, slag being withdrawn through taphole 138.
  • a gas offtake 14111 is provided above the slag pool 144.
  • the floor of the slag separation zone C slopes downwards from the slag weir 137 to the level of the surface of the metal in the smelting zone A.
  • Banks 135, 136 of dolomite or other suitable basic refractory material are provided on opposite sides of the passages a and b between the smelting zone A and the re fining zone D, and between the smelting zone A and the slag separation zone C, the banks 135, 136 serving to restrict the width of the passage a and b for the reasons hereinafter described.
  • FIGURE 28 a furnace is shown in which the refining zone D is divided by a slag barrier into two refining zones 130a and 1341b.
  • the said slag barrier is formed by banks 146 of dolomite, fluid-cooled U-tubes 147 and a layer of slag 148 which builds up on the tubes 147.
  • FIGURES 30 and 31 apparatus is shown in which a pressurised fluidised bed unit 160 is provided for preheating and prereducing fine unagglomerated iron ore or concentrates.
  • the iron ore or concentrates are blended with a proportion of carbonaceous material (e.g. about 4% by weight of powdered coal) and the blended mixture 166 is fed into hopper 163, from which it is fed by means of screw feeder 164 into the pressurised fluidised unit bed 160, the feed rate into the unit being controlled by the speed of screw feeder 164.
  • carbonaceous material e.g. about 4% by weight of powdered coal
  • a burner 168 e.g. an oxy-oil burner
  • a valve 169 for removal of fines is connected to the lower end of the fluidised bed unit 160 and delivers hot combustion gases upwardly through grate 170 into and through the fluidised bed 161. Heat is also generated in the fluidised bed 161 by partial burning in the bed of the coal mixed with the concentrate.
  • the preheated and partially prereduced concentrates leave the fluidised bed unit 160 through a heavily lagged Wear-resistant and heat-resistant pipe 165 which is connected to a feeder-burner device 172.
  • the device 172 projects through the side wall of the furnace F, for example in the position occupied by lance 128a in FIG- URES 25 to 28, and injects preheated prereduced particulate concentrates into the bath of molten material in the smelting zone A of the furnace, preferably 'with sufficient velocity to ensure that the concentrates penetrate through the slag layer and into the molten metal therebeneath.
  • the feeder burner device 172 is shown in more detail in FIGURE 31 and comprises a central pipe 165 through which the hot concentrates are fed, a series of oil or propane pipes 176, a series of oxygen or air pipes 177, and a surrounding water jacket 178.
  • the fine concentrates issuing in the form of a jet 179 from the end of pipe 165 are heated by the surrounding annulus of burner flames 180 formed by combustion of the jets of oil or propane and oxygen issuing from the ends of pipes. 176, 1'77.
  • the heat in the exit gases from all embodiments of the invention may be used for such purposes as preheating feed materials, and/or incoming air, or, if they contain carbon monoxide, they may be used for pre-reducing as well as preheating.
  • the preheating and either p-re-reduction or pre-oxidation is carried out in hot cyclones (not shown) in association with turbulent gas-solids mixing chambers.
  • the preheated and either pre-reduced or pre-oxidised particulate materials are then transferred in the hot gases directly to the ports or lances to the circulatory smelting zone.
  • Preheating of the raw materials may be carried out using a conventional downwardly converging cyclone. Hot gases are led through the usual tangential pipe to the upper end of the cyclone. A short distance from the entry to the cyclone, the appropriate ores are fed into the pipe from an auxiliary pipe as fines. To induce the entry of the fines, the main pipe may be formed as a venturi adjacent to the auxiliary pipe.
  • these difliculties may be avoided by (a) ensuring lat vigorous turbulence is maintained in the refining zone, a by jetting with gas, and (b) incorporating a little fine 3211 or oil or other hydrocarbon with the oxygen-contining gas blown into the refining zone.
  • Nickel having a much higher melting point than coper, must be produced at temperatures 300 to 400 C. igher than those of the reactions necessary to refine white Jetal (Cu S).
  • the process and apparatus of this invention can be aplied to the smelting of lead-zinc ores, preferably oxidised, r mixtures of roasted lead-zinc sulphide concentrates or ven slags containing lead and zinc.
  • lead-zinc ores preferably oxidised, r mixtures of roasted lead-zinc sulphide concentrates or ven slags containing lead and zinc.
  • he injection into the feed and primary smelting zone takes lace as with other concentrates or finely crushed material, he fuel-reductant preferred being powdered coke breeze u" low hydrogen content char or coal, although other :arbonaceous fuels can be used.
  • the fines )nly may be fed in through the tuyeres or lances while ump ore or slag is fed to the furnace via a heat exchanger shaft or kiln.
  • the zinc In the smelting of zinc bearing materials, the zinc is lot tapped with the reduced lead, or other less volatile netal, but leaves the furnace in the vapor phase in the hot :arbon monoxide containing gases.
  • gaseous zinc may :hen be condensed or absorbed in an appropriate separate apparatus, as for example the lead splash condenser developed by the Imperial Smelting Corporation Ltd. of Avonmouth, England.
  • the comoustible gases may be used for preheating air or lump feed materials or be used to entrain further fines to be fed to the furnace.
  • Example 1 Lead smelting in an annular furnace of the type shown in FIGURES 4 to 6 and lined with chrome magnesite bricks.
  • Lead concentrates containing were preheated in a screw type preheater to approximate 300 C. and injected with a hot 50:50 mixture of air and oxygen into the feed zone A of the furnace at position 38 at the rate of 1000 lbs. per hour.
  • the furnace had previously been charged with lead bullion and preheated to 1050 C. so that it had a fully liquid bath of lead covered with a high lead content slag.
  • Lime sand containing about 40% SiO and 50% CaCO was incorporated with the lead concentrates in the ratio of 50 parts of concentrates to one of lime sand. Further air-oxygen mixture was injected through lances at positions 41, 42 and 43 (see FIGURE 4). After the furnace had been operating for about 4 hours the proportion of oxygen in the injected gas was reduced somewhat so that the gas mixture contained approximately 35% oxygen. At this stage the lead being tapped from taphole 46 was relatively pure bullion containing about 98.9% lead, 0.42% sulphur, and the balance being made up of antimony, arsenic, zinc, copper, cadmium, gold and silver.
  • the slag tapped from taphole 50 contained Percent Lead 15 ZnO 12 FeO 10.5 Sulphur 1.5
  • Example 2 Copper smelting in an annular furnace of the general shape shown in FIGURE 1 and line with chrome-magnesite bricks.
  • the furnace chamber was first heated by oil firing to 1250 C. and charged with matte from a previous smelting operation, such matte containing about Percent Copper 40 Iron 32 Sulphur 29 After the bath had become completely liquid the feeding of concentrates through lances at positions 38 and 39 was begun.
  • the concentrates contained Percent Copper 24.2 Iron 30.5 Sulphur 32.1 Insolubles 7.0
  • a 50:50 air-oxygen mixture was blown in through lances at positions 41, 42, 43 and 44. After operating for about half an hour, white metal containing approximately copper was being tapped at 46. The copper tenor progressively increased as the amounts of oxygen-containing gases were increased relative to the feed rate, which was maintained at 1400 lbs. per hour.
  • the metal being tapped at 46 contained over 99% copper, the major impurity being sulphur, 0.75%, which, however, was concentrated in the top layer of the metal on solidification.
  • Example 3 Further trials with copper concentrates were carried out in a graphite-lined furnace of the linear type shown in FIGURES 9 to 11, the furnace preheating and other conditions being similar to that in Example 2. After approximately 2 hours operation a copper product containing 99.1% metallic copper was tapped continuously in a small stream from a bottom taphole at position 46. The slag tapped continuously at 50 contained approximately 1.5% copper.
  • Example 4 Several copper smelting trials were carried out in a two-branched furnace of the general shape shown in FIGURES 14 to 17. This furnace had graphite bricks lining the refining branch and chrome-magnesite bricks lining the feed-primary smelter zone. These trials gave improved performance in respect of general heat conservation and reduction of copper content in the slag tapped at 46. Using the same feed materials as in Examples 2 and 3 the slag tapped at 50 contained 0.5% copper, while the copper metal tapped at 46 was of the same degree of purity as in Example 3 and could readily be cast into anodes for electrolytic refining.
  • Example 5 Iron smelting at the rate of 0.5 tons per hour.
  • a crome-magnesite lined furnace of the type shown in FIGURES 13 to 20 preheated by oil burners to 1300 C., and charged first with pig-iron containing 4.1% carbon, 1.3% silicon to give a molten bath, a 50:50 mixture of ore and brown coal char were injected in hot air at feed positions 78 and 79 after preheating by heat exchange from exit combusted gases to about 350 C. The finely ground ore contained.
  • Pellets were made from a 80-20 mixture of finely ground ore and brown coal char of the above compositions. On discharge from the hot end of the kiln 76 into the chute 61 these pellets were found to contain 90.1% metallic iron and 4.2% carbon.
  • the carbon content in the steel tapped at 46 was not reduced below 0.6% so as to maintain relatively low melting point and good fluidity in the liquid steel. However, it is possible to lance the furnace metal with oxygen so as to produce steel of any desired carbon content down to the mild steel range.
  • Example 6 Copper sulphide flotation concentrates from Mount Morgan, Australia, containing 24.2% copper, 30.5% iron, 32.1% sulphur and 7.0% insolu'bles were smelted in a furnace substantially as shown in FIGURES 21 to 24.
  • the furnace was preheated and charged with matte of approximately 65 to 70% Cu level from a previous smelt-ing campaign.
  • dry concentrates at a temperature of between 200 and 350 C. were blown through the lance 38 (having an internal diameter of approximately 0.65 inch) air under pressure of between 20 to. 30 p.s.i. being introduced through the annular space (having a radial width of approximately 0.1 inch) between the lance 38 and tube 91.
  • the feed rate of concentrates during the run was about 600 lbs. per hour.
  • the lance 38 was disposed in the manner shown in FIGURES 21 and 22 and terminated approximately 10 inches above the surface of the-bath in the smelting zone A.
  • the lances 43, 44 and 45 were approximately disposed as shown in FIGURES 1 and 2 and terminated approximately at the level of the interface between the matte and the slag.
  • Siliceous flux (e.g. silica sand) was added by mechanical or pneumatic feeders through ports 102.
  • the sulphur dioxide-bearing gases formed were withdrawn through gas oiftake 37 and were taken via hot cyclones to a sulphuric acid plant.
  • the burner 108 was operated generally with a neutral flame, the oil burner 109 was operated with an oxidising flame, and the oil burners 110 and 111 were operated with reducing flames.
  • the copper product withdrawn from taphole 46 contained from 99.0 to 99.5% copper depending on the amount of further oxidising treatment it received by the jetting of the oxidising flame from burner 109.
  • a typical analysis of the copper product was as follows:
  • the slag withdrawn from taphole 50 usually contained less than 0.5% copper and for long periods when the furnace was operating under steady state conditions the copper-in-slag was in the range 0.30 to 0.36%.
  • the preferred range for SiO in slag is 36 to 42% while that for FeO is 45 to 50%.
  • the presence of between 2 and 5% of CaO-l-MgO in the slag seems to be advantageous.

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Description

June 20, 1967 H. K. WORNER ,6
I DIRECT SMELTING OF METALLIC ORES Filed Aug. 4, 1966 11 Sheets-Sheet 1 I/V, Vf/V T02 #0144420 A- WOENEQ A Tram/5.5?
June 1967 H. K. WORNER DIRECT SMELTING OF METALLIC ORES l1 Sheets-Sheet 3 Filed Aug. 4, 1966 55 as I \0 .7 VE V 701? #0014420 K WQEIVE/Z June 20, 1967 H. K. WORNER 3,325,571
I DIRECT SMELTING 0F METALLIC ORES Filed Aug. 4, 1966 l]. Sheets-Sheet 5 zm Awme 4 #010420 If. M/dQ/VER June 20, 1967 H. K. WORNER 3,326,671
DIRECT SMELTING OF METALLIC ORES Filed Aug. 4, 1966 ll Sheets-Sheet 7 June 20, 1967 H. K. WORNER DIRECT SMEL'IING OF METALLIC ORES Filed Aug. 4, 1966 ll Sheets-Sheet 8 June 20, 1967 H. K. WORNER 3,326,671
DIRECT SMELTING OF METALLIC ORES Filed Aug. 4, 1966 11 Sheets-Sheet 1o June 20, 1967 H. K. WORNER 3,326,671
DIRECT SMEL'I'ING OF METALLIC ORES Filed Aug. 4, 1966 11 sheets-sheet 11 .TA/VE/l/ 7012 #010 420 1% Ween/5Q United States Patent DIRECT SMELTING 0F METALLIC ORES Howard K. Worner, 18 The Blvd. N. Balwyn,
Melbourne, Victoria, Australia Filed Aug. 4, 1966, Ser. No. 570,270 Claims priority, application Australia, Apr. 11, 1963, 29,505/ 63 36 Claims. (Cl. 75--40) ABSTRACT OF THE DISCLOSURE A method for continuously producing metals from ore and concentrate base material by providing in a furnace chamber intercommunicating smelting, refining and slag separation zones having molten material therein. The base material is fed to the molten material in the smelting zone as the molten material continuously flows from the smelting zone to the refining zone from where metal is withdrawn while the slag produced flows into the separating zone from where it is withdrawn. Oxygen containing gas is introduced into the molten material during its passage through the furnace chamber.
This application is a continuation-in-part of my copending US. patent application Ser. No. 355,661, filed Mar. 20, 1964, and now abandoned. I
This invention relates to the direct smelting of metallic ores and concentrates, and refers particularly to a method for the production of metals directly from particulate ores and concentrates and to apparatus for car rying out such method. The term metal in this Specification includes metals, alloys and other metal-nich prod-ucts of the smelting operation.
The invention is applicable to the smelting of ores or concentrates (e.g. sulphide ores or. concentrates) of metals such as copper, nickel and lead, and to the production of iron and steel from oxide ores or concentrates of iron. It is also applicable to the smelting of zinc bearing ores and concentrates, subject to the considerations referred to subsequently in this specification.
While particularly suited to the direct smelting of finely particulate or powdered ores and-concentrates, the invention can, with the appropriate modifications hereinafter described, be usedfor smelting ores or concentrates a proportion of which is in lump form or all or a pro portion of which comprises pelletisedor otherwise agglomerated fines. The term particulate in this specification refers to and includes solid materials of the abovementioned types, the particles of which are fineenough to be handled in tubes pneumatically or 'by gravity flow. In most cases the particles are smaller than one centimetre in diameter. As used herein in the specification and claims the term ores includes ores, or concentrates of ores, in any form including pelletized form, and in the case of iron prereduced material in any form.
The invention makes use of the fast reactions between oxygen-containing gas, such as air, oxygen or oxygenenriched air, and hot particulate oxidisable solid materials such as sulphides or solid"carbonaceous fuels. The heat generated by these fast reactions provides the energy necessary to keep the melting'and smelting operations going. The invention may therefore be described as autogenous melting and/ or smelting. It differs from other autogenous smelting operations, in part, in that it involves reactions under or in proximity to' the surface of a flowing stream ofmoltenmaterial, such reactions being induced by injecting or feeding particulate reactants and an oxygencontaining gas onto or under the surface of the aforementioned flowing stream.
The movement of the flowing stream of molten ma- See terial may be induced by the design of the furnace, by the angles of impingement on the molten material of the particulate raw materials and/ or of the injected gases, or by the introduction into the furnace of an initiator stream of molten material from an auxiliary furnace or smelter, or by a combination of two or more of these factors. The auxiliary furnace (if employed) may be contiguous with or separate from the furnace of this invention and may be of any suitable type, and'the flow of molten material therefrom may be reduced or discontinued when the smelting operation in the furnace of this invention has been stabilized.
The invention in one general form is a method of producing metals directly from particulate ores and concentrates which comprises the steps of: preparing in a furnace chamber a bath of molten material from the particulate ores or concentrates and/or from the products of a previous melting or smelting operation; maintaining in the furnace a feed and primary smelting zone, a refining zone and a slag settling zone; causing the molten material to flow in a stream continuously through the chamber and away from the feed and primary smelting zone; feeding the ores or concentrates in particulate form into or onto the stream of molten material in the feed and primary smelting zone; introducing an oxygen-containing gas into or onto the stream of molten material during its passage through the furnace chamber; developing an exothermic reaction with the bath of molten material between the oxygen-containing gas and at least one component of the molten material; withdrawing slag from the slag settling zone; withdrawing molten material from the refining zone; and withdrawing gaseous products of reaction from the furnace chamber. As used herein in the specification and claims the term into, in reference to introduction and contact of a gas or ore with molten material, includes, without limitation, introduction of the gas or ore from either above, at or below the surface of the molten material.
The invention in another general form is a method of producing metals directly from particulate ores or concentrates which comprises the steps .of: preparing in a furnace chamber a bath of molten material from the particulate ores or concentrates and/or from the prod ucts of a previous melting or smelting operation; maintaining in the furnace chamber a feed and primary smelting zone; a secondary smelting zone, a slag settling zone, and a refining zone; causing the molten material to flow in a stream continuously through the chamber from the feed and primary smelting zone to the secondary smelting zone and to the refining zone; causing slag formed on the surface of the molten material to flow to the slag settling zone; feeding the particulate ores or concentrates into or onto the stream of molten material in the feed and primary smelting zone; introducing an oxygen-containing gas into or onto the stream of molten material at two or more points therealong; developing an exothermic reaction within the bath of molten material between the oxygen-containing gas and at least one component of the molten material; tapping slag from the slag settling zone, tapping metal from the refining zone; and withdrawing gaseous products of reaction from the furnace chamber.
The invention in another general form is apparatus for carrying out the abovementioned method, comprising: a furnace having a substantially enclosed chamber in which is maintained a continuously flowing stream of molten material, means for feeding particulate ores or concentrates into or onto the stream of molten material, means for introducing oxygen-containing gas into or onto the stream of molten material, means for withdrawing slag from the furnace at one point, means for withdrawing molten metal from the furnace at another point, and
means for discharging gaseous products from the furnace. I
The term lance in this specification includes a tube raving one or more discharge outlets through which pariculate material and/ or oxygen-containing gas, such as .ir, oxygen or oxygen-enriched air, and/ or gaseous, liquid If particulate solid fuel and/ or fluxes or other additives, s or are injected or fed into the furnace.
The refractories used to line the furnace are appro wriate to the reactants used and products formed in the urnace and to the temperature and other conditions exsting in the furnace. Alternatively in certain zones of he furnace fluid-cooled jackets may be used to form the walls and/or roof of the furnace.
The furnace of this invention when viewed in plan may )e linear, annular, rectangular, D-shaped, U-shaped or )f other suitable shape, including the forms of the invenion illustrated in the accompanying drawings.
In this specification the term annular furnace refers :o a furnace whether circular or otherwise in which one )r more continuous circuits is provided for the fiow of molten material, and in which portion of the molten naterial is caused to recycle from the refining zone into ;he feed and primary smelting zone. The invention includes, but is not limited to, the use of an annular furnace.
The slag settling zone and the refining zone of the furnace may comprise branches or extensions to the furnace which connect with the smelting zone or zones, and in one form of the invention the slag settling zone is disposed to connect with the stream of molten material before the latter reaches the refining zone. The gas ofitake is conveniently located above the slag settling zone or branch.
The particulate raw materials (which are preferably preheated) are jetted or fed into or onto the molten material in the furnace at the feed and primary smelting zone. These materials may be fed by screw feeders, pneumatic injection or other means. Oxygen-containing gas is preferably introduced with the particulate materials, and may also be introduced into the furnace at other positions so as to impinge onto or into the flowing stream of molten material.
It has also been found desirable to ensure vigorous motion, stirring or turbulence of the molten material at the point of introduction of the particulate materials, i.e., in the feed and primary smelting zone, and the injection or feeding of the particulate materials and/or oxygen-containing gas is preferably effected so as to achieve this condition.
The heat developed within the bath of molten material by exothermic reactions may be supplemented by the burning of particulate materials in transit to the bath and/or by burning of combustible gases generated by reactions within the bath and/or by combustion of carbonaceous fuel added with the particulate raw materials.
The invention makes use of modern techniques for dispensing and injecting powders along with air or air enriched with oxygen or other gas. In some cases a proportion of the particulate materials and any lump materials may be fed into the bath under gravity or introduced by screw feeders.
The invention takes advantage of the speed of reaction between hot fine particulate sulphides on the one hand or finely particulate coal or the like on the other, and hot oxygen-containing gases. As soon as the particulate materials enter the hot furnace and certainly when they strike or enter the molten bath they react vigorously. In the case of sulphides, exothermic reactions of the type occur, and in the case of coal, blown or fed in with fine ore, the carbon in the coal burns to CO and a little to CO but such CO tends, in the feed and primary smelting zone, immediately to react with further hot particles of coke or char producing CO according to the reaction The carbon monoxide is then available both to reduce metal oxides and to be burnt and thus give off more heat as the gases pass on through the furnace.
It might be thought that because particulate materials are being injected into the furnace, serious dust losses would result. This, in fact, is not the case because the rapidly heating, and in some cases partially molten, particles are readily absorbed into the bath (which is usually in a frothing or bubbling condition) into which they are fed or injected. In effect, a sort of scrubbing action is achieved.
Means such as a gas barrier may be provided in the furnace above the stream of molten material to substantially prevent reverse flow of gases.
The slag settling zone or branch is preferably constructed with a ridge or slag overflow region and with the floor of said zone or branch sloping upwardly from the furnace chamber to the ridge or slag overflow region. The end of the floor of the slag zone or branch adjacent to the smelting chamber of the furnace is preferably located at or near the intended level of the matte or metal in the said chamber, and the level of the ridge or slag overflow is preferably located above the intended level of the matte or metal.
The conditions in the slag settling zone, and in the lower region of the exit end of the refining zone from which the metal is tapped, are preferably quiescent. Gases may be caused to impinge into or onto the surface of the material in the refining zone, or a portion thereof, in such a manner as to create a countercurrent flow of slag in the refining zone, on the surface of the molten metal or matte, away from the metal outlet.
By the invention, a significant composition gradient is developed between the feed zone and the point at which the metal is tapped.
Some forms of the invention are illustrated in the accompanying drawings, wherein:
FIGURE 1 is -a view in sectional plan of one form of furnace;
FIGURE 2 is a view in sectional elevation on the line 2-2 of FIGURE 1;
FIGURE 3 is a view in section on the line 33 of FIGURE 1;
FIGURE 4 is a view in sectional plan of another form of furnace;
FIGURE 5 is a view in sectional elevation on the line 55 of FIGURE 4;
FIGURE 6 is a view in section on the line 6-6 of FIGURE 4;
FIGURE 7 is a view in sectional plan of a further form of furnace;
FIGURE 8 is a view in sectional elevation on the line 8-8 of FIGURE 7;
FIGURE 9 is a perspective view of a further form of furnace;
FIGURE 10 is a view in sectional plan of the furnace shown in FIGURE 9;
FIGURE 11 is a view in sectional elevation on the line 11-11 of FIGURE 10;
FIGURE 12 is a view in sectional plan of a further form of furnace;
FIGURE 13 is a view in sectional elevation on the line 13-13 of FIGURE 12;
FIGURE 14 is a perspective view of a further form of furnace;
FIGURE 15 is a view in sectional plan of the furnace shown in FIGURE 14;
FIGURE 16 is a view in sectional elevation on the line 1616 of FIGURE 15;
FIGURE 17 is a view in sectional elevation on the line 1717 of FIGURE 15;
FIGURE 18 is a view in sectional plan of a further form of furnace;
FIGURE 19 is a view in sectional elevation on the line 1919 of FIGURE 18; and
FIGURE is a view in sectional elevation on the line 2020 of FIGURE 18;
FIGURE 21 is a sectional plan view of a substantially U-shaped furnace constructed in accordance with the invention;
FIGURE 22 is a view in sectional elevation on the line 22-22 of FIGURE 21;
FIGURE 23 is a view in sectional elevation on the line 23-23 of FIGURE 21;
FIGURE 24 is a view in sectional elevation on the line 24-24 of FIGURE 21;
FIGURE 25 is an isometric view of apparatus for the treatment of ores or concentrates, particularly of iron oxide ores or concentrates, according to the invention;
FIGURE 26 is a sectional plan view of the furnace shown in FIGURE 25;
FIGURE 27 is a view in sectional elevation of the furnace shown in FIGURE 25 FIGURE 28 is a sectional plan view of a modified form of furnace;
FIGURE 29' is a view in sectional elevation taken on the line 2929 of FIGURE 26;
FIGURE 30 is a view in sectional elevation of a modified ore feed arrangement, and
FIGURE 31 is a perspective view of a device for feeding and'pre-heating particulate ores or concentrates.
Referring to the drawings, where the same reference characters are used to indicate like or corresponding parts, and with particular reference to FIGURES 1 to 3, the furnace shown in these figures is of the annular type and comprises an external cricular wall 30, an internal circular wall 31, a floor 32, and annular chamber 33, and a domed annular roof 34. A slag settling branch 35 and a refining branch 36 are connected to the annular chamber 33. A gas oiftake 37 is provided above the slag settling branch 35.
Particulate ores or concentrates, preferably preheated, and where necessary preblended with carbonaceous fuel, are fed pneumatically. or by other means into the annular chamber through lances or powder feeders 38, 39 which project through the roof 34 or through the external wall 30.
A bath of molten material 40 is formed in the bottom or trough of the chamber 33 and is caused to fiow generally in an anti-clockwise direction as shown in FIGURE 1. In this figure the direction of flow of metal or matte is shown by arrows in full lines and the direction of flow of slag is shown by arrows in dotted lines. The particulate ores or concentrates are fed into or onto the molten material 40 in the feed and primary smelting zone A.
Oxygen-containing gas is injected into or onto the molten material 40 through lances 41, 42 which project into the secondary smelting zone B, and also through lances 43, 44, which project into the refining zone D within the refining branch 36, and if desired oxygencontaining gas may also be injected with the particulate material through lances 38, 33.
The lances 38, 39, 41, 42, 43, 44 and 45- are shown in the drawings to terminate a short distance above the surface of the molten material 40 so that the particulate materials and/or gases injected therethrough are directed onto the surface of the molten material, but in an alternative form of the invention (not shown) any of the lances vmay be designed and arranged to project beneath the surface of the molten material.
All orsome of the lances 3 8, 39, 41 and 42 may be tilted 0r inclined at an angle to the vertical in order to impart or to assist in imparting forward movement to the molten material 40 in the required direction in the chamber 33 (anti-clockwise in the drawing). The lances 43, 44, 45 are inclined in the reverse'direction to that of the flow of metal or matte in the refining branch 36, so as to create a countercurrent flow of slag in the re- .fining branch 36 away from the taphole 46 and towards the annular chamber 33. The metal or matte flows outwardly in the refining branch 36 and is discharged through taphole or outlet 46.
The slag branch 35 is provided with an outwardly and upwardly sloping floor 47, a ridge or slag overflow 48, a slag pool or reservoir 49 and a slag settling zone C.
A gas barrier 51 may be provided in the annular chamber 33 to extend from the roof 34 almost to the surface of the molten material 40.
In the case of sulphide concentrate smelting, the process achieves the continuation of the oxidation of sulphur, iron and some other readily oxidisable elements commenced in the feed zone A. The sulphur leaves the bath as S0 while the iron and other oxidisable elements enter the slag by a reaction of the type In the case of iron ore smelting, the oxygen-containing gas blown in at positions such as 41 and 42 serves to combust any unburnt carbon or carbon monoxide leaving the feed zone A and entering the secondary smelting zone B. The oxygen-containing gas blown in at positions such as 43, 44, 45 serves to oxidise out the carbon from the semi-steel bath to bring it to the desired value before steel is tapped through taphole 46.
Slag formed in the feed and primary smelting zone A and secondary smelting zone B flows slowly and quiescently out through the slag branch 35, over the ridge or overflow 48 and is discharged through taphole 50. The slag in the slag branch 35 is kept liquid by heat exchange (from the'hot gases moving'to the gas ofitake, 37).
The metal or matte continues to flow around the annulus and a proportion enters the refining branch 36, where it is withdrawn continuously or semi-continuously through taphole 46. Any slag which forms in the refining branch 36 is caused to flow countercurrently back into the annular chamber 33 and portion of it may be recycled and portion may flow countercurrent to the matte or metal and leaves the furnace at 50.
Gases generated by lancing at positions such as 38, 39', '41, 42 tend to move concurrently with the molten material, whereas gases generated by lancing at positions such as 43, 44, 45 may tend to move countercurrent to the molten material, at least in portion of the annulus.
The proportion of the molten material which is recycled into the feed and primary smelting zone A is not critical and is determined mainly by the relative rate of feed of solids to the rate of tapping of slag through taphole 50 and of metal through taphole .46.
ing pool of molten material may be built up from either concentrates plus flux, and/or from the products of a previous run. p
In addition to the fluxing materials which may be added with the particulate ore or concentrates, more finely particulate flux can appropriately be added through one or more of the lances in the refining branch 36 such as, for example, throughlance 45. Alternatively itmay be added in a position near to lance 45 through ports or side doors (not shown). The slag generated by the reaction of this flux addition tends to move countercurrent to the matte or metal. In the smelting or sulphides this assists in the removal of the last traces of unwanted elements, for example, iron in the case of copper and nickel, and in the case of steelmaking, the countercurrent slag. flow assists refining with respect to sulphur and phosphorus The floor of the refining branch 36 may be more or :ss horizontal in the case of iron and steelmaking. In he case of smelting of sulphides, however, it is often .n advantage for the said floor to slope gently downwards mm the main furnace floor towards the taphole 46 as hown at 36' in FIGURES 11, 13 and 16. -In the case If both copper and lead production, it is advantageous have at the end of the refining branch 36, a sump l6 (such as that shown in FIGURE 13) which is prefrably substantially deeper than the rest of the bath of he refining branch 36. The submerged taphole 46 or .yphon can appropriately be connected to the bottom of his sump 46'.
It is advantageous if the metal in the bottom of the :ump 46 is cooled to within about 80 C. to 150 C. at its melting point before it passes out through the subnerged taphole or syphon. This is to cause as much as Jossible of the contained sulphur to come out of soluion in the metal before the metal leaves the furnace. The cooling may be achieved by use of a deep sump or )y cooling fluid passing through metal coolers -or by slowing cold air through a lance or lances deeply submerged in the sump or by other suitable means.
When it is desired to incorporate lump materials, as for example cement copper in the case of copper smeltlng, these materials can be added through ports or doors (not shown) in the walls or roof of either the annulus portion of the furnace or of the refining branch 36.
It will be appreciated that widely differing chemical reactions and conditions are involved in each of the several applications of the invention to different ores or concentrates. Thus, in the smelting of sulphides oxidising conditions exist right around the annulus, while in the smelting of iron oxides the atmosphere, at least in the feed zone A, is a reducing one.
In the latter case, it is an advantage to have the bath covered with solid carbonaceous material in the feed zone and for some distance along the path of liquid flow thereafter. The necessary carbon in the form of pulverulent coal or char is added along with the fine ore or it may be jetted into the bath through auxiliary lances in the vincinity of the feed zone A in the case of iron and steel production. The carbon content of the bath metal in the annulus portion of the furnace is maintained in the semi-steel range so that there is adaquate interna fuel in the metal for heat gene-ration during the final lancing with oxygen-containing gas in the refining branch 36.
The sensible heat in the exit gases, in each form of the invention, may be used for a number of purposes, such as drying and preheating the particulate feed materials, preheating the oxygen-containing gases, for steam raising or for other purposes. In the case of iron smelting, some of the gas, utilized with fine coal or char, may also be used for partial pre-reducing of the particulate ores before feeding to the furnace.
In order to drain the furnace at the end of a campaign or run a drain plug can be provided at a convenient position; alternatively the whole furnace may be designed to permit slight tilting towards the taphole 46.
In FIGURES 4, and 6 a furnace of rectangular shape is shown. The references have the same connotations as in FIGURES 1, 2 and 3.
The furnace has an outer wall 30 and an internal island wall 55. The lances 41 and 42 enter the furnace through the side wall 56 and are disposed at an angle as shown in FIGURE 4 in order to impart forward movement to the molten material which flows from the feed and primary smelting zone A towards the secondary smelting zone B and then continues its anticlockwise movement within the furnace.
It will be noted that the gas space 57 above the molten material to the left of the island wall 55, as viewed in FIGURES 4 and 5, is considerably greater than the gas space 58 on the feed zone side of the wall 55. This has the advantage that the gas flow rate is lowered in the 8 larger space 57 thus enabling entrained particulate materials and slag droplets to fall back into the bath before the gases pass out through the slag branch 35 and gas olftake 37.
In the case of the smelting of iron ore, the slowing down of the gases in this space 57 also facilitates the burning of the carbon monoxide leaving the feed zone A. It is advantageous in this particular application to blow the oxygen-containing gas'through turbulant jets at positions such as 41 and 42. This assists the complete combustion of carbon monoxide and of fine entrained char or coke particles.
In FIGURES 7 and 8 a furnace is shown having two island walls 55 and 55', two feed and primary smelting zones A and A, and two sets of lances 38, 3-? and 38' and 39', through which particulate materials may be in troduced either concurrently or alternately into the feed zones A and A respectively. Lances 41 and 41' inclined in opposite directions, are provided for injection of oxygen-containing gas. In this furnace the slag branch 35 is disposed opposite to the refining branch 36. p
In the case of this furnace it is possible to shut down and effect repairs to one of the feed zones A or A while the other is still operating. If, for the purpose of fettling or for other reasons it is desired to shut down and isolate one of the feed zones, a refractory barrier (not shown) is lowered through removable portions of the roof 34 of the furnace at positions at the ends of the island wall 55 and 55' as the case may be.
In FIGURES 9, 10 and 11 a linear furnace is shown having a central feed and primary smelting zone A into which particulate raw materials and (if desired) oxygencontaining gas, are injected through inclined lances 38, 39. These lances are arranged approximately tangentially to the feed zone A, so as to impart a circulatory or rotary movement to the molten material in said zone. The chamber is narrowed on either side of said zone A as shown at 62 and 63 in FIGURE 10, thereby providing an approximately circular feed zone in which the said circulatory movement of the molten materials is facilitated.
The slag branch 35 and the refining branch 36 are disposed on opposite sides of and are connected to the central feed zone A as shown in FIGURE 10. The furnace may be tilted through a slight angle on rollers 59 to facilitate fettling of refractories and/ or draining of liquids at the end of a campaign. A stationary chimney is provided over the gas oiftake aperture 37 at the end of the furnace.
In FIGURES 12 and 13 a further modified form of furnace is shown having a circular feed smelter zone A into which particulate materials and (if desired) oxygencontaining gas are injected through lances 38, 39 which are angled so as to impart circulatory movement to the molten material in zone A. The slag branch 35 extends laterally at right angles to the refining branch 36.
In a modified form of the invention (not shown) the branch leading to the secondary smelting zone B, slag settling zone C and refining zone D, which are arranged in a straight line in said branch, extends tangentially from and connects with the feed and primary smelter zone A. Circulation is imparted to the molten material in the feed zone A, preferably in a direction which directs such material along the tangential branch to the secondary smelting zone B and hence to zones C and D. The branch may be narrowed between zones C and D. In one alternative arrangement (not shown) two circulatory feed zones may be provided in which circulation of molten material is effected in opposite directions, and the said branch leading to zones B, C and D is connected cen trally to the chamber containing the two circulatory feed zones.
In the form of the invention shown in FIGURES 14 to 17, a U-shaped furnace is shown in which the slag branch I 35 and refining branch 36 are parallel and side-by-side.
Particulate feed materials are injected through either or both lances 38, 39. Oxygen-containing gas is injected through lances 41, 42 and lances 43, 44, 45. Particulate materials and/or oxygen-containing gas may be fed together or separately through lances 38, 39 as desired. By appropriate choice of angles of the lances 38, 39, 41, 42 and of the gas pressures used, it is possible to achieve a relatively long residence time of the reacting particulate materials in the gas space above the circulatory feed zone A before such materials impinge on the molten material in said zone. A conical or domed roof (not shown) may be provided over the circulatory feed zone A and the said roof may be of good quality refractory or may be fluid cooled metal. A gas otftake chimney 37 is provided at the end of the slag branch 35.
In the FIGURES -18 to 20, an annular furnace is shown which is provided with a central core 60 of lump ore or concentrates or agglomerated or pelletised fines. The pelletised ore or the like is fed through chute 75 into a rotary kiln 76, heat exchange being effected to the incoming pelletised ore from the exit gases passing up stack 70. The residence time in the kiln 76 is sufiicient to enable some pre-oxidation or pre-reduction (as the case may be) of the pelletised ore or concentrate to be effected before the material is discharged into the vertical shaft 61 and thence into the centre of the furnace. Further particulate ore or concentrate may be charged to the feed-smelter zone A of the furnace by means of hoppers 77 and screw feeders 78, 79. Oxygen-containing gas is introduced through lances 41, 42, 43, 44 and 45. Other features of the furnace are similar to those of the furnace shown in FIGURES l to 3.
It is undesirable to have too high a velocity of the hot gases passing out through kiln 76 otherwise dust losses may be considerable. This, however, is usually only a problem if much fine unagglomerated material is fed in via chute 75.
In some applications, and particularly with iron and steel manufacture, it is advantageous to add a little 'fine char or lump coal or charcoal to the feed to the kiln 76. These carbonaceous lumps help not only to ensure maintenance of strongly reducing conditions in the kiln but to prevent welding of the iron in the pellets or'other lumps to each other or to the inside walls of the kiln. I
It has been found to be a desirable practice to blend in with fine iron ore or concentrates before pelletising, a proportion of finely ground coke breeze, or char or noncoking coal. The proportion is normally between and 20%.] Such carbonaceous material in the pellets facilitates fast reduction reactions in the kiln 76; it also helps to prevent the aforementioned welding ofpellets to each other and to the kiln walls. Some of this carbon usually remains in the hot pellets as they are discharged into the smelting zone of the furnace proper where it is dissolved in the bath of hot metal. It then becomes part of the internal fuel in the bath as it moves into the refining zone D under the air and/ or oxygen jets.
The pellets may be formed with or without binding agents and with or without fluxes incorporated.
If it should be found that the carbon monoxide-rich gases passing up shaft 61 to the kiln are too hot, they may appropriately be cooled by injecting steam in through a lance or port (not shown). Such steam, apart from its cooling effect, enters into a gas shift reaction with the very hot carbon monoxide thus:
The hot hydrogen thus produced acts as a highly efficient reductant in the kiln 76. The furnace shown in FIGURES 21 to 24 is particularly useful for the direct smelting of copper sulphide concentrates by the process of the invention and this embodiment of the invention,
and connects at 88 with a refiner branch or zone D and at 89 with a slag separation branch or zone C. The portions 90a, 90b of the slag separation zone C connecting with the smelting zone A are constricted in width relative to the remaining portion 900 of said zone C.
Warm dry copper sulphide concentrates are introduced in particulate form into the feed and smelting zone A through lance 38 which in this embodiment is arranged concentrically within an outer tube 91, air and sometimes air plus a little oil being blown under pressure through the annular space between the lance 38 and tube 91. Siliceous flux may be added with the concentrates. The feed material is preferably preheated (e.g. to a temperature of between 200 C. and 650 C.) prior to or during its introduction into the furnace.
The concentrates are injected into the bath of molten material 40 in the smelting zone A in such .a manner as to cause turbulence and agitation of the molten material.
The lance 38 is arranged at an angle of between about 40 to about 80 to the horizontal as shown in FIG URE 22 so as to cause the concentrates to impinge at an angle onto the surface of the molten material 40 in zone A. The lance 38 is disposed approximately tangentially to the circular smelting zone A so as to cause circulation of the molten material in the said zone in the direction shown by the arrows 92 in FIGURE 21. The direction of circulation of the molten material 40 in zone A is such that slag flowing from the refiner zone D to the slag separation zone C travels by the longest route through zone A so that it has a maximum residence time in zone A. The floor 93 of zone A of the furnace is substantially horizontal.
The refiner branch D of the furnace is of elongated rectangular shape in plan and its floor 94 slopes downwardly from the junction of zone D with zone A to a V-shaped passage or sump 95 formed in the end wall 83 through which molten copper 97 flows from the refiner zone D. The angle of slope of the floor 94 is between 3 and 30", preferably between 5 and 10. The lower end 96 of the end wall 83 projects downwardly below the level of copper 97 in the refiner zone D. The sump 95 communicates with a metal reservoir 98 formed in furnace extension 99. A copper tapho le 46 communicates with the metal reservoir 98 below the slag level in the refiner zone D and preferably at approximately the same level as that of the matte-white metal complex 100 in the refiner branch D.
'Lances 43, 44, 45 project, at an angle to the horizontal,
through the side wall 80 of the furnace and air under pressure is injected through the lances 4 3, 44, 45 into the molten material in the refiner zone D, the angle of impingement of the lances and the air pressure being such that the injected air bubbles out into the molten matte and creates vigorous turbulence of the molten material in the said zone D.
Silica or siliceous ore flux is added mechanically or pneumatically through ports 102 in the internal wall 84. The ports 102 are disposed more or less directly opposite to the lances 43, 44, 45 so that the silicious' material delivered from the ports 102 serves to protect the refractory of the wall 84 from erosion due to splashing of molten material caused by air injection through the said lances.
A main gas offtake 37 for sulphur dioxide bearing furnace gases is provided above the exit end of the refiner zone D. A port 103 is provided in the roof 86 through 1 l vhich lump concentrates or lump ore may be added to he molten material in the refiner zone D.
The slag separation zone C of the furnace is provided vith a slag weir 48 which may be air-cooled, a slag pool )r well 4-9, a matte taphole 104 through which matte 105 nay be tapped at infrequent intervals as required, a slag aphole 50, and an auxiliary gas oiftake 106. The floor 47 )f the slag separation zone C slopes gently upwards from he smelting zone A to the slag weir 48. A port 107 is )rovided in the roof 86 through which a reducing agent, L1Ch as iron sulphide, in the form of pyrites, pyrrhotite r low grade copper sulphide concentrates, and/or a caraonaceous fuel, may be added to the molten material in the ;lag separation zone C.
An oil burner 108 projects through the wall 80 into the smelting zone A and its flame is directed onto the surface of the molten material 40 therein; an oil burner 109 projects into the furnace extension 99 and its flame which is preferably oxidising is directed onto the surface of the molten copper in the copper reservoir 98, and products of combustion enter the furnace proper through port 109a; and oil burner 110 projects through the side wall 81 and its flame, which is preferably reducing, is directed onto the surface of the slag in the slag separation zone C; and an oil burner 111 projects through the end wall 83 and its flame, which is preferably reducing, is directed onto the surface of the slag in the slag pool 49.
The oil burner 110 is directed transversely of the general direction of the flow of the slag through the slag separation zone C soas to impart a gentle circulation or eddying motion to the slag in the zone C as indicated by the arrows 112 in FIGURE 21. The oil burner 111 is directed onto the slag in the slag pool 49 so as to cause a gentle circulation of the said slag as shown by the arrows 113 in FIGURE 21. The circulation of slag indicated at 112, 113 is substantially confined to the surface layers of the said slag and is not such as to disturb the generally quiescent conditions prevailing in the slag separation zone C and slag pool 49. The said circulation of slag is such as to increase the residence time of the slag in the slag separation zone C and the slag pool 49 and thus provide greater opportunity for the elimination of copper from the slag by settling out of fine prills of metal or matte.
Inspection and sampling ports 114 and 115 are formed in the end wall 82 and side wall 81 respectively, and are closed by refractory plugs 116, 117 respectively. Port 115 is a convenient entry point for the addition to the bath of a reducing agent, such as a carbonaceous fuel, e.g. coal.
In the operation of the furnace shown in FIGURES 21 to 24, copper sulphide concentrates are blown in with air under pressure through lance 38 into the bath of molten material in the smelting zone A, the furnace having been preheated and charged with molten matte. Vigorous turbulence and circulation of the molten material in the smelting zone A is effected. Operation of the oil burner 108 assists the circulation of the molten material in zone A and supplements the heat provided by the oxidation of the sulphur and iron in the incoming concentrates.
Matte generated in the smelting zone A, being heavier than the slag, settles towards the floor of the furnace and then as it becomes heavier by the progressive elimination of sulphur and iron it gravitates down the sloping floor of the refiner branch D towards the sump 95. Air under pressure is blown through the lances 43, 44, 45 into the molten material in the refiner branch D so as to create vigorous turbulence in the said material and to effect the progressive oxidation of sulphur and iron in the matte in said zone D. Siliceous flux in the form of silica sand or finely crushed copper ore is added through ports 102. The sulphur dioxide formed by oxidation of the sulphur enters the furnace gases which are withdrawn through gas oiftake. The iron oxide formed in zone D reacts with the silica to form slag.
Lump copper sulphide concentrates are added through port 103, for the purpose of minimizing the formation of magnetite in the upper layers of the slag in the zone B. The slag 101 formed in zone D rises to the surface of the matte and as it accumulates on the surface of said matte it flows towards the smelting zone A countercurrently to the flow of matte in zone D. Copper 97 formed by oxidation of the white metal in the matte-white metal complex 100 in zone D settles out in the lower part of the zone D and flows through the sump 95 into the metal reservoir 98 from which it is tapped at taphole 46-. An oxidising flame from burner 109 may be directed onto the surface of the copper in reservoir 98 in order tooxidise residual sulphur. Alternatively, the sulphur may be removed in a separate furnace.
The slag flowing countercurrently in the refiner zone D flows through the smelting zone A in the general direction of the circulation of material in zone A, that is, mainly adjacent to the outer wall of zone A, its residence time in zone A being thereby increased. During its passage through zone A the freshly melted concentrates, now substantially in the form of droplets of matte, are agitated with and dispersed into the said slag. This has the effect of stripping of a substantial proportion of copper in the slag stream passing through zone A. The slag then flows from zone A into the relatively quiescent slag separation zone C, passing through the restricted portions 90a, 90b, of zone C into the larger portion 900 of said zone. Gentle circulation of the surface layers of the slag in portion 900 of zone C is effected by means of burner 110. Pyrites, or another source of iron sulphide, and/or a solid carbonaceous material, is added through port 107 and/or port 115 in order to effect removal of residual copper from the slag. The products of combustion of the burners 110 and 111 and sulphur dioxide from the combustion of the pyrites added through port 107 are withdrawn through auxiliary gas olftake 106.
It is desirable .to maintain reducing conditions in the slag separation zone C in order to assist the separation of copper from the slag and also to convert to and to maintain in the ferrous state as much as possible of the iron in the slag, thereby minimizing the formation of undesirable massive wall and hearth accretions of magnetite. As indicated, a convenient manner of maintaining such reducing conditions in the slag separation zone C is by the addition of pyrites or another source of iron sulphide :and/or by the addition of a reducing agent and/or by having a gentle jet of a reducing flame (such as, for example, from burner 110) directed at a relatively low angle over the slag so that gentle circulation is achieved and the iron sulphide and/or reducing agent is distributed and dispersed over the slag surface.
The gentle circulation induced in the slag separation zone C (for example by burner 110) increases the residence time of the top layers of slag in that zone and thus provides greater opportunity for matte particles to settle alnd thus decrease the amount of copper tapped in the s ag.
Another manner of creating reducing conditions in the slag separation zone C is by prilling iron sulphide with oil so that when the oiled pyrites is added to the slag separation zone C the oil burns with a reducing flame at the slag surface. This also promotes the melting and incorporation into the slag of iron sulphide which itself acts as a reducing agent.
Matte which settles out from the slag in the slag separation zone C flows down the sloping floor 47 of said zone C towards the smelting zone A in a direction countercurrent to the general flow of slag through the zone C. The slag, after separation of matter and stripping of copper in zone C, flows over the slag weir 48 into the slag pool 49 where fin-al separation of matte and copper therefrom is effected. Burner 111 is operated to raise the temperature of the slag in pool 49, to impart a gentle circulation of said slag in the pool 49 to ensure maximum matte 13 separation, and, being a reducing flame, to minimize magnetite formation in the slag. Slag is tapped through slag taphole 50.
Referring to FIGURES '25 to 27, the numeral 120 represents a disc pelletiser in which composite pellets P are produced from oxide ores or concentrates, carbonaceous material and a binder.
The pellets P are fed from pan feeder 121 into one end of a rotary metallisin g kiln 122. In the heat recuperator 124 air is admitted at pipe 125 and products of combustion are removed through stack 126. The rotary kiln 122 delivers the metallised pellets into a column 123 which is mounted vertically over the smelting zone A of the furnace F, preferably to one side of said zone A. The pellets fall by gravity in the column 123 into the circulating and turbulent bath of molten material in the said smelting zone. Air or steam, or both, may be admitted to column 123 through heat resitsant retractable pipes 127a and 127b. Gases may be withdrawn through gas offtake 141a, which is controlled by a slide valve 145. A similar control valve (not shown) may be provided on stack 126.
The furnace F is provided with a substantially circular smelting zone A and with an elongated refining zone D and a sla-g separation zone C which are connected to the smelting zone A by restricted openings or passages a and b respectively.
The furnace F is of U-shape, the refining zone D and slag separation zone C being arranged parallel to one another and separated by wall 131, but it will be understood that furnaces of other shapes may be employed.
Lances 128a and 128b project through the wall of the furnace F into the smelting zone A, and are inclined downwardly and are also arranged substantially tangentially to the zone A. Air and/or particulate carbonaceous material may be injected into the bath in zone A through lances 128a and 128b. A burner 129 also projects tangentially into the smelting zone A. Apertures 142, 142' are provided in the roof of the furnace F through which fine lump basic refractories, e.g. dolomite, or other materials may be added to the bath, the apertures 142 being located above the smelting zone A and the aperture 142' being located above the slag separation zone C." Coke or other slag conditioning agents may be added to the slag separation zone through aperture 143.
Lances 132, 133, 134 pr-oject (if desired at an incline) into the refining zone D, and oxygen-containing gas is injected through the said lances into the turbulent molten material in the zone D. The lances 132, 133, 134 preferably incline downwandly and towards zone A. Metal is withdrawn from-the refining zone D at taphole 139 and underneath slag baffle 140.
A slag weir 137 is provided in the slag separation zone C over which slag overflows-into a slag pool 144, slag being withdrawn through taphole 138. A gas offtake 14111 is provided above the slag pool 144. The floor of the slag separation zone C slopes downwards from the slag weir 137 to the level of the surface of the metal in the smelting zone A.
Banks 135, 136 of dolomite or other suitable basic refractory material are provided on opposite sides of the passages a and b between the smelting zone A and the re fining zone D, and between the smelting zone A and the slag separation zone C, the banks 135, 136 serving to restrict the width of the passage a and b for the reasons hereinafter described.
In FIGURE 28, a furnace is shown in which the refining zone D is divided by a slag barrier into two refining zones 130a and 1341b. The said slag barrier is formed by banks 146 of dolomite, fluid-cooled U-tubes 147 and a layer of slag 148 which builds up on the tubes 147.
In FIGURES 30 and 31, apparatus is shown in which a pressurised fluidised bed unit 160 is provided for preheating and prereducing fine unagglomerated iron ore or concentrates. The iron ore or concentrates are blended with a proportion of carbonaceous material (e.g. about 4% by weight of powdered coal) and the blended mixture 166 is fed into hopper 163, from which it is fed by means of screw feeder 164 into the pressurised fluidised unit bed 160, the feed rate into the unit being controlled by the speed of screw feeder 164.
A combustion chamber 167 fired by a burner 168 (e.g. an oxy-oil burner) and having a valve 169 for removal of fines, is connected to the lower end of the fluidised bed unit 160 and delivers hot combustion gases upwardly through grate 170 into and through the fluidised bed 161. Heat is also generated in the fluidised bed 161 by partial burning in the bed of the coal mixed with the concentrate.
The preheated and partially prereduced concentrates leave the fluidised bed unit 160 through a heavily lagged Wear-resistant and heat-resistant pipe 165 which is connected to a feeder-burner device 172. The device 172 projects through the side wall of the furnace F, for example in the position occupied by lance 128a in FIG- URES 25 to 28, and injects preheated prereduced particulate concentrates into the bath of molten material in the smelting zone A of the furnace, preferably 'with sufficient velocity to ensure that the concentrates penetrate through the slag layer and into the molten metal therebeneath.
Any fines which leave the upper end of the fluidised bed unit 160 through pipe 173 pass through cyclone 174 and are returned through pipe 175 to the fluidised bed.
The feeder burner device 172 is shown in more detail in FIGURE 31 and comprises a central pipe 165 through which the hot concentrates are fed, a series of oil or propane pipes 176, a series of oxygen or air pipes 177, and a surrounding water jacket 178. The fine concentrates issuing in the form of a jet 179 from the end of pipe 165 are heated by the surrounding annulus of burner flames 180 formed by combustion of the jets of oil or propane and oxygen issuing from the ends of pipes. 176, 1'77.
The heat in the exit gases from all embodiments of the invention may be used for such purposes as preheating feed materials, and/or incoming air, or, if they contain carbon monoxide, they may be used for pre-reducing as well as preheating. i
In another form of this invention, the preheating and either p-re-reduction or pre-oxidation is carried out in hot cyclones (not shown) in association with turbulent gas-solids mixing chambers. The preheated and either pre-reduced or pre-oxidised particulate materials are then transferred in the hot gases directly to the ports or lances to the circulatory smelting zone.
Preheating of the raw materials may be carried out using a conventional downwardly converging cyclone. Hot gases are led through the usual tangential pipe to the upper end of the cyclone. A short distance from the entry to the cyclone, the appropriate ores are fed into the pipe from an auxiliary pipe as fines. To induce the entry of the fines, the main pipe may be formed as a venturi adjacent to the auxiliary pipe.
In the cyclone the solids will be separated from the gases in conventional fashion, the solids falling and the gases escaping upwards.
Similar apparatus to that which has recently been de veloped to entrain fine coal in air or other gas streams and feed it through the tuyeres of iron blast furnaces may be used advantageously with this present invention.
In the smelting of nickel-iron sulphides, difiiculties may develop if the conditions in the refining zone or branch are allowed to become too quiescent and oxidising towards the metal outlet end. It has been found that in the batchwise conversion of nickel sulphide to metal, jetting of oxygen onto 'a non-turbulent bath can lead to excessive localised build-up of nickel oxide which may form impenetrable layers and virtually stop the refining reaction. In this invention these difliculties may be avoided by (a) ensuring lat vigorous turbulence is maintained in the refining zone, a by jetting with gas, and (b) incorporating a little fine 3211 or oil or other hydrocarbon with the oxygen-contining gas blown into the refining zone. By this means it possible to achieve vigorous stirring without excessive xidation of the hot bath, with its consequent tendency form regions high in nickel oxides.
Nickel, having a much higher melting point than coper, must be produced at temperatures 300 to 400 C. igher than those of the reactions necessary to refine white Jetal (Cu S).
The process and apparatus of this invention can be aplied to the smelting of lead-zinc ores, preferably oxidised, r mixtures of roasted lead-zinc sulphide concentrates or ven slags containing lead and zinc. With such materials, he injection into the feed and primary smelting zone takes lace as with other concentrates or finely crushed material, he fuel-reductant preferred being powdered coke breeze u" low hydrogen content char or coal, although other :arbonaceous fuels can be used. Alternatively, the fines )nly may be fed in through the tuyeres or lances while ump ore or slag is fed to the furnace via a heat exchanger shaft or kiln.
In the smelting of zinc bearing materials, the zinc is lot tapped with the reduced lead, or other less volatile netal, but leaves the furnace in the vapor phase in the hot :arbon monoxide containing gases. Such gaseous zinc may :hen be condensed or absorbed in an appropriate separate apparatus, as for example the lead splash condenser developed by the Imperial Smelting Corporation Ltd. of Avonmouth, England. After recovery of the zinc, the comoustible gases may be used for preheating air or lump feed materials or be used to entrain further fines to be fed to the furnace.
The following examples illustrate the invention.
Example 1 Lead smelting in an annular furnace of the type shown in FIGURES 4 to 6 and lined with chrome magnesite bricks.
Lead concentrates containing were preheated in a screw type preheater to approximate 300 C. and injected with a hot 50:50 mixture of air and oxygen into the feed zone A of the furnace at position 38 at the rate of 1000 lbs. per hour. The furnace had previously been charged with lead bullion and preheated to 1050 C. so that it had a fully liquid bath of lead covered with a high lead content slag.
Lime sand containing about 40% SiO and 50% CaCO was incorporated with the lead concentrates in the ratio of 50 parts of concentrates to one of lime sand. Further air-oxygen mixture was injected through lances at positions 41, 42 and 43 (see FIGURE 4). After the furnace had been operating for about 4 hours the proportion of oxygen in the injected gas was reduced somewhat so that the gas mixture contained approximately 35% oxygen. At this stage the lead being tapped from taphole 46 was relatively pure bullion containing about 98.9% lead, 0.42% sulphur, and the balance being made up of antimony, arsenic, zinc, copper, cadmium, gold and silver.
The slag tapped from taphole 50 contained Percent Lead 15 ZnO 12 FeO 10.5 Sulphur 1.5
16 Example 2 Copper smelting in an annular furnace of the general shape shown in FIGURE 1 and line with chrome-magnesite bricks.
The furnace chamber was first heated by oil firing to 1250 C. and charged with matte from a previous smelting operation, such matte containing about Percent Copper 40 Iron 32 Sulphur 29 After the bath had become completely liquid the feeding of concentrates through lances at positions 38 and 39 was begun. The concentrates contained Percent Copper 24.2 Iron 30.5 Sulphur 32.1 Insolubles 7.0
A 50:50 air-oxygen mixture was blown in through lances at positions 41, 42, 43 and 44. After operating for about half an hour, white metal containing approximately copper was being tapped at 46. The copper tenor progressively increased as the amounts of oxygen-containing gases were increased relative to the feed rate, which was maintained at 1400 lbs. per hour.
After about three hours of operation the metal being tapped at 46 contained over 99% copper, the major impurity being sulphur, 0.75%, which, however, was concentrated in the top layer of the metal on solidification.
Silicious flux in the form of fine d-une sand of the following composition Percent SiO 97.2 Al O 1.7 FeO 0.5
was added at positions 44 and 45 and the slag being tapped at 50 contained Percent FeO 41.7
Example 3 Further trials with copper concentrates were carried out in a graphite-lined furnace of the linear type shown in FIGURES 9 to 11, the furnace preheating and other conditions being similar to that in Example 2. After approximately 2 hours operation a copper product containing 99.1% metallic copper was tapped continuously in a small stream from a bottom taphole at position 46. The slag tapped continuously at 50 contained approximately 1.5% copper.
Example 4 Several copper smelting trials were carried out in a two-branched furnace of the general shape shown in FIGURES 14 to 17. This furnace had graphite bricks lining the refining branch and chrome-magnesite bricks lining the feed-primary smelter zone. These trials gave improved performance in respect of general heat conservation and reduction of copper content in the slag tapped at 46. Using the same feed materials as in Examples 2 and 3 the slag tapped at 50 contained 0.5% copper, while the copper metal tapped at 46 was of the same degree of purity as in Example 3 and could readily be cast into anodes for electrolytic refining.
Example 5 Iron smelting at the rate of 0.5 tons per hour. In a crome-magnesite lined furnace of the type shown in FIGURES 13 to 20 preheated by oil burners to 1300 C., and charged first with pig-iron containing 4.1% carbon, 1.3% silicon to give a molten bath, a 50:50 mixture of ore and brown coal char were injected in hot air at feed positions 78 and 79 after preheating by heat exchange from exit combusted gases to about 350 C. The finely ground ore contained.
Supplementary to the feed of particulate materials at 78 and 79, an approximately equal amount of iron bearing material was fed via a vertical refractory chute 61 from a preheating-prereducing kiln 76 into the centre chamber in the form of metallised pellets which themselves had been produced in the kiln by heating up to 1200 C. by partial combustion of the hot CO-rich gases leaving the furnace.
Pellets were made from a 80-20 mixture of finely ground ore and brown coal char of the above compositions. On discharge from the hot end of the kiln 76 into the chute 61 these pellets were found to contain 90.1% metallic iron and 4.2% carbon.
After about two hours operation the metal flowing around the annulus was found to have a composition of 3.1% carbon. By further lancing with oxygen at 99.5% purity at positions 43 and 44 in the refining branch 36 it was possible to oxidise out the carbon to produce any desired grade of steel at taphole 46. Burnt lime containing 95.2% CaO was injected as flux through a port near lance 45.
In most of the iron smelting experiments conducted, the carbon content in the steel tapped at 46 was not reduced below 0.6% so as to maintain relatively low melting point and good fluidity in the liquid steel. However, it is possible to lance the furnace metal with oxygen so as to produce steel of any desired carbon content down to the mild steel range.
Example 6 7 Copper sulphide flotation concentrates from Mount Morgan, Australia, containing 24.2% copper, 30.5% iron, 32.1% sulphur and 7.0% insolu'bles were smelted in a furnace substantially as shown in FIGURES 21 to 24. The furnace was preheated and charged with matte of approximately 65 to 70% Cu level from a previous smelt-ing campaign. After the bath was completely liquid, dry concentrates at a temperature of between 200 and 350 C. were blown through the lance 38 (having an internal diameter of approximately 0.65 inch) air under pressure of between 20 to. 30 p.s.i. being introduced through the annular space (having a radial width of approximately 0.1 inch) between the lance 38 and tube 91. The feed rate of concentrates during the run was about 600 lbs. per hour. The lance 38 was disposed in the manner shown in FIGURES 21 and 22 and terminated approximately 10 inches above the surface of the-bath in the smelting zone A.
Air under pressure between 12 and 20 p.s.i. was blown through the high chromium steel lances 43, 44, 45 (each having an internal diameter of approximately 0.7 inch) into the molten material in the refiner branch. The lances 43, 44 and 45 were approximately disposed as shown in FIGURES 1 and 2 and terminated approximately at the level of the interface between the matte and the slag.
Siliceous flux (e.g. silica sand) was added by mechanical or pneumatic feeders through ports 102. The sulphur dioxide-bearing gases formed were withdrawn through gas oiftake 37 and were taken via hot cyclones to a sulphuric acid plant. Additional ore or concentrates, preferably in lump form, and preferably in amounts ranging from 10% to 40% of the input of concentrates added through lance 38, were added through port 103, to reduce the formation of magnetite in the refining zone D.
The burner 108 was operated generally with a neutral flame, the oil burner 109 was operated with an oxidising flame, and the oil burners 110 and 111 were operated with reducing flames.
Pyrites, pre-prilled by rolling in a drum with a small proportion of a heavy mineral oil, was added through port 107 in amount equivalent to about 7% of the concentrate-s added through lance 38. Sulphur dioxide-bearing gases were withdrawn through gas oiftake 106. The hot gases drawn off through ofitake 106, still containing some partially combusted hydrocarbons, were used for drying ad preheating the incoming concentrates in separate apparatus (not shown).
Copper as formed was withdrawn from taphole 46, slag was withdrawn almost continuously from taphole 50, and small quantities of matte were tapped at approximately 48 hour intervals from taphole 104.
The copper product withdrawn from taphole 46 contained from 99.0 to 99.5% copper depending on the amount of further oxidising treatment it received by the jetting of the oxidising flame from burner 109. A typical analysis of the copper product was as follows:
Percent Copper 99.10 Sulphur 0.80 Iron 0.004 Lead 0.005 Antimony 0.007 Bismuth 0.005 Arsenic 0.005 Nickel 0.02 Zinc 0.004 Other 0.05
The slag withdrawn from taphole 50 usually contained less than 0.5% copper and for long periods when the furnace was operating under steady state conditions the copper-in-slag was in the range 0.30 to 0.36%. These figures are comparable to the best reverberatory furnace practice, where, of course, only matte is being produced and that on a batchwise basis.
. A typical analysis of slag was as follows:
. Percent Si0 38.3 FeO 1 49.7 Other oxides 10.9
S 0.7 Cu 0.36
The preferred range for SiO in slag is 36 to 42% while that for FeO is 45 to 50%. The presence of between 2 and 5% of CaO-l-MgO in the slag seems to be advantageous.
Example, 7

Claims (1)

1. A METHOD FOR THE CONTINUOUS PRODUCTION OF METALS FROM ORES COMPRISING THE STEPS OF PROVIDING IN A BATH OF MOLTEN MATERIAL A SMELTING ZONE, A REFINING ZONE AND A SLAG SEPARATION ZONE, THE SAID ZONES BEING SUBSTANTIALLY SEPARATE FROM BUT IN COMMUNICATION WITH EACH OTHER; INTRODUCING ORE SUBSTANTIALLY CONTINUOUSLY INTO THE MOLTEN MATERIAL IN THE SMELTING ZONE AND SMELTING THE ORE OR CONCENTRATE IN SAID ZONE; INCLUDING TURBULENCE AND CIRCULATION OF THE MOLTEN MATERIAL IN THE SMELTING ZONE; CAUSING MOLTEN MATERIAL TO FLOW IN A STREAM CONTINUOUSLY FROM THE SMELTING ZONE TO THE REFINING ZONE; INJECTING AN OXYGEN-CONTAINING GAS INTO THE STREAM OF MOLTEN MATERIAL IN THE REFINING ZONE; CAUSING SLAG PRODUCED TO FLOW SUBSTANTIALLY CONTINUOUSLY TO THE SLAG SEPARATION ZONE; INDUCING FLOW OF SLAG COUNTER-CURRENT TO THE FLOW OF MOLTEN METAL IN AT LEAST A PART OF THE REFINING ZONE; MAINTAINING SUBSTANTIALLY QUIESCENT CONDITIONS IN THE SLAG SEPARATION ZONE; WITHDRAWING SLAG FROM THE SLAG SEPARATION ZONE; AND WITHDRAWING MOLTEN METAL FROM THE REFINING ZONE.
US570270A 1963-02-21 1966-08-04 Direct smelting of metallic ores Expired - Lifetime US3326671A (en)

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GB6523/64A GB1003026A (en) 1963-02-21 1964-02-17 Continuous production of furnace products
SE2015/64A SE304581B (en) 1963-02-21 1964-02-19
US345987A US3288451A (en) 1963-02-21 1964-02-19 Continuous production of furnace products
DE19641519752 DE1519752A1 (en) 1963-02-21 1964-02-20 Method and device for the continuous production of molten silicates, melting furnace products
FR964764A FR1387509A (en) 1963-02-21 1964-02-21 Process for producing molten materials from particulate raw materials
BE644174D BE644174A (en) 1963-02-21 1964-02-21
DE1964F0042480 DE1294022B (en) 1963-02-21 1964-04-01 Hearth furnace for continuous simultaneous smelting and refining of ores and processes for operating the hearth furnace
GB14818/64A GB1055935A (en) 1963-02-21 1964-04-09 Direct smelting of ores and concentrates
AT309464A AT266461B (en) 1963-02-21 1964-04-09 Process for the continuous smelting of small-sized ores or concentrates in a hearth furnace and device for carrying out the process
FI640758A FI43791C (en) 1963-02-21 1964-04-10 Method for continuous smelting of ores and concentrates
NL6403867A NL6403867A (en) 1963-02-21 1964-04-10
SE4457/64A SE315741B (en) 1963-02-21 1964-04-10
BE646429A BE646429A (en) 1963-02-21 1964-04-10
YU498/64A YU31189B (en) 1963-02-21 1964-04-10 Uredaj za neprekidno jednovremeno topljenje i rafiniranje rude i/ili koncentrata
FR970642A FR1429265A (en) 1963-02-21 1964-04-11 Method and apparatus for the production of metals directly from ores and concentrates in particulate form
LU45859D LU45859A1 (en) 1963-02-21 1964-04-11
US390042A US3326672A (en) 1963-02-21 1964-08-17 Refining of metals and alloys
DE19641458306 DE1458306B2 (en) 1963-02-21 1964-08-18 DEVICE AND METHOD FOR REFINING LIQUID METALS
GB34235/64A GB1064826A (en) 1963-02-21 1964-08-21 Refining of metal and alloys
FR986427A FR1405775A (en) 1963-02-21 1964-08-27 Improvements to continuous metal refining processes and furnaces
BE652436D BE652436A (en) 1963-02-21 1964-08-28
US620568A US3432157A (en) 1963-02-21 1966-11-08 Apparatus for refining metals
US619108A US3463472A (en) 1963-02-21 1967-01-05 Apparatus for the direct smelting of metallic ores
MY197089A MY7000089A (en) 1963-02-21 1970-12-31 Direct smelting of ores and concentrates

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AU29505/63A AU281236B2 (en) 1963-04-11 Direct smelting of metallic ores and concentrates
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AU3473863 1963-08-28
AU3803463 1963-11-25
AU4124464 1964-02-24
US61910867A 1967-01-05 1967-01-05

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US4514217A (en) * 1983-05-17 1985-04-30 Boliden Aktiebolag Method of producing lead from sulphidic lead raw-material
US4676825A (en) * 1985-06-21 1987-06-30 Centro Sperimentale Metallurgico Spa Hot metal desulphurizing and dephosphorizing process
US4701217A (en) * 1986-11-06 1987-10-20 University Of Birmingham Smelting reduction
AU583906B2 (en) * 1985-04-03 1989-05-11 Cra Services Limited Smelting process
US5069715A (en) * 1990-04-02 1991-12-03 Regents Of The University Of Minnesota Direct smelting process and apparatus
EP0524399A2 (en) * 1991-07-26 1993-01-27 Steel Technology Corporation Two-zone countercurrent smelter system
US5466278A (en) * 1990-12-11 1995-11-14 Metallgesellschaft Aktiengesellschaft Process for the manufacture of steel
US5746805A (en) * 1995-07-18 1998-05-05 Metallgesellschaft Aktiengesellschaft Process for the continuous manufacture of steel
US5853452A (en) * 1992-05-23 1998-12-29 The University Of Birmingham Synthetic rutile production

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US3463472A (en) * 1963-02-21 1969-08-26 Conzinc Riotinto Ltd Apparatus for the direct smelting of metallic ores
US3437475A (en) * 1964-11-23 1969-04-08 Noranda Mines Ltd Process for the continuous smelting and converting of copper concentrates to metallic copper
US3462263A (en) * 1965-08-11 1969-08-19 John H Walsh Reduction of iron ore
US3473918A (en) * 1966-06-17 1969-10-21 Anaconda Co Production of copper
US3525604A (en) * 1966-10-21 1970-08-25 Edward M Van Dornick Process for refining pelletized metalliferous materials
US3514280A (en) * 1967-10-19 1970-05-26 Sherwood William L Continuous steelmaking method
US3634065A (en) * 1968-02-16 1972-01-11 Conzinc Riotinto Ltd Method for refining metals
US3725044A (en) * 1968-12-07 1973-04-03 Mitsubishi Metal Corp Method of continuous processing of sulfide ores
US3663207A (en) * 1969-10-27 1972-05-16 Noranda Mines Ltd Direct process for smelting of lead sulphide concentrates to lead
US3865579A (en) * 1970-01-05 1975-02-11 Koppers Co Inc Method and apparatus for the production of steel
US3847595A (en) * 1970-06-29 1974-11-12 Cominco Ltd Lead smelting process
US3769002A (en) * 1970-07-08 1973-10-30 Int Nickel Co Reduction of nickel and cobalt oxides in a molten metal bath of controlled oxygen content
US3861905A (en) * 1971-02-16 1975-01-21 Forderung Der Eisenhuttentechn Process for accelerating metallurgical reactions
US3980283A (en) * 1971-02-16 1976-09-14 Gesellschaft Zur Forderung Der Eisenhuttentechnik Mbh Apparatus for performing a continuous metallurgical refining process
US3868248A (en) * 1971-10-06 1975-02-25 Foseco Int Deoxidising molten non-ferrous metals
US3791816A (en) * 1972-03-30 1974-02-12 Kaiser Aluminium Chem Corp Production of nickel from nickel-bearing materials
US3929465A (en) * 1972-11-14 1975-12-30 Sam Proler Method employing barrier means to submerge particles in a molten metal stream
US3941587A (en) * 1973-05-03 1976-03-02 Q-S Oxygen Processes, Inc. Metallurgical process using oxygen
US3849120A (en) * 1973-06-25 1974-11-19 T Norman Smelting of copper-iron or nickel-iron sulfides
US4162915A (en) * 1976-09-06 1979-07-31 Metallurgie Hoboken-Overpelt Process for treating lead-copper-sulphur charges
FR2363634A1 (en) * 1976-09-06 1978-03-31 Metallurgie Hoboken LEAD-COPPER-SULFUR LOAD TREATMENT PROCESS
US4177063A (en) * 1977-03-16 1979-12-04 The Glacier Metal Company Limited Method and apparatus for reducing metal oxide
US4304595A (en) * 1977-07-22 1981-12-08 Boliden Aktiebolag Method of manufacturing crude iron from sulphidic iron-containing material
US4178174A (en) * 1977-08-24 1979-12-11 The Anaconda Company Direct production of copper metal
WO1980001287A1 (en) * 1978-12-19 1980-06-26 Anaconda Co Direct production of copper metal
EP0016595A1 (en) * 1979-03-09 1980-10-01 National Research Development Corporation A method of recovering non-ferrous metals from their sulphide ores
US4399983A (en) * 1980-03-05 1983-08-23 Arbed S.A. Apparatus for the production of liquid iron, especially for directly producing liquid iron from ore
EP0053594A1 (en) 1980-12-01 1982-06-09 Boliden Aktiebolag The manufacture of lead from sulphidic lead raw material
US4396426A (en) * 1980-12-01 1983-08-02 Boliden Aktiebolag Manufacture of lead from sulphidic lead raw material
US4514222A (en) * 1981-11-26 1985-04-30 Mount Isa Mines Limited High intensity lead smelting process
US4514217A (en) * 1983-05-17 1985-04-30 Boliden Aktiebolag Method of producing lead from sulphidic lead raw-material
AU583906B2 (en) * 1985-04-03 1989-05-11 Cra Services Limited Smelting process
US4676825A (en) * 1985-06-21 1987-06-30 Centro Sperimentale Metallurgico Spa Hot metal desulphurizing and dephosphorizing process
US4701217A (en) * 1986-11-06 1987-10-20 University Of Birmingham Smelting reduction
EP0266975A1 (en) * 1986-11-06 1988-05-11 The University Of Birmingham Smelting reduction
EP0427710A1 (en) * 1986-11-06 1991-05-15 The University Of Birmingham Smelting reduction
US5069715A (en) * 1990-04-02 1991-12-03 Regents Of The University Of Minnesota Direct smelting process and apparatus
US5466278A (en) * 1990-12-11 1995-11-14 Metallgesellschaft Aktiengesellschaft Process for the manufacture of steel
EP0524399A2 (en) * 1991-07-26 1993-01-27 Steel Technology Corporation Two-zone countercurrent smelter system
EP0524399A3 (en) * 1991-07-26 1994-02-02 Steel Tech Corp
US5378260A (en) * 1991-07-26 1995-01-03 The United States Of America As Represented By The Department Of Energy Two-zone countercurrent smelter system and process
US5853452A (en) * 1992-05-23 1998-12-29 The University Of Birmingham Synthetic rutile production
US5746805A (en) * 1995-07-18 1998-05-05 Metallgesellschaft Aktiengesellschaft Process for the continuous manufacture of steel

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