US3326672A - Refining of metals and alloys - Google Patents
Refining of metals and alloys Download PDFInfo
- Publication number
- US3326672A US3326672A US390042A US39004264A US3326672A US 3326672 A US3326672 A US 3326672A US 390042 A US390042 A US 390042A US 39004264 A US39004264 A US 39004264A US 3326672 A US3326672 A US 3326672A
- Authority
- US
- United States
- Prior art keywords
- slag
- metal
- refining
- chamber
- outlet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B19/00—Obtaining zinc or zinc oxide
- C22B19/04—Obtaining zinc by distilling
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/04—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in tank furnaces
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/12—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in shaft furnaces
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/10—Making spongy iron or liquid steel, by direct processes in hearth-type furnaces
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C1/00—Refining of pig-iron; Cast iron
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
- C21C5/42—Constructional features of converters
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/56—Manufacture of steel by other methods
- C21C5/567—Manufacture of steel by other methods operating in a continuous way
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B13/00—Obtaining lead
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0026—Pyrometallurgy
- C22B15/0028—Smelting or converting
- C22B15/003—Bath smelting or converting
- C22B15/0045—Bath smelting or converting in muffles, crucibles, or closed vessels
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0026—Pyrometallurgy
- C22B15/0054—Slag, slime, speiss, or dross treating
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B15/00—Obtaining copper
- C22B15/0026—Pyrometallurgy
- C22B15/006—Pyrometallurgy working up of molten copper, e.g. refining
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B23/00—Obtaining nickel or cobalt
- C22B23/02—Obtaining nickel or cobalt by dry processes
- C22B23/025—Obtaining 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B25/00—Obtaining tin
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B5/00—General methods of reducing to metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/10—Reduction of greenhouse gas [GHG] emissions
- Y02P10/134—Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S75/00—Specialized metallurgical processes, compositions for use therein, consolidated metal powder compositions, and loose metal particulate mixtures
- Y10S75/957—Continuous refining of molten iron
Definitions
- the invention is concerned particularly with methods and apparatus in'which the said oxidation is achieved by blowing or feeding an oxygen-containing gas into or onto a slowly flowing stream of molten crude metal or matte, through a succession of lances or tuyeres disposed along the path of flow of the molten material. It applies, for example, to the continuous refining of molten pig iron to steel and to the continuous conversion of copper or nickel mattes to copper and nickel respectively.
- metal includes crude metals, alloys and mattes
- each of the terms oxygen and oxygen-containing gas includes oxygen, air and other suitable oxygen-containing gases.
- FIGURE 7 is a view in sectional plan of an L-shaped furnace
- the location of the gas off-take 26 in or on the branch 18 rather than in the roof of the main refining chamber 10 also simplifies the roof design of the latter and permits freer access by crane to the whole length of the roof in the refining chamber 10. This is of importance when it is desired to make rapid replacement of a burnt-out section of the roof or to effect other repairs to the top of the furnace.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
- Glass Melting And Manufacturing (AREA)
- Vertical, Hearth, Or Arc Furnaces (AREA)
- Glass Compositions (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
June 20, 1967 H. K. WORNER 3,326,672
REFINING OF METALS AND ALLOYS Filed Aug. 17, 1964 y r x 46 E 25 10b 29 ii 5 Sheets-Sheet l June 20, 1967 H. K. WORNER REFINING OF METALS AND ALLOYS 3 Sheets-Sheet 2 Filed Aug. 17, 1964 United States Patent 3,326,672 REFINING 0F METALS AND ALLOYS Howard Knox Worner, New Lambton, New South Wales,
Australia, assignor to Farnsfield Limited, Nassau, Bahamas Filed Aug. 17, 1964, Ser. No. 390,042 Claims priority, application Australia, Aug. 28, M63, 34,738/63 12 Claims. (Cl. 75-46) This invention relates to improvements in methods of and apparatus for continuously or semi-continuously refining crude metals or alloys or mattes to metals, in which the oxidation of unwanted substances is achieved by reactions involving oxygen, or oxygen-containing gas. The invention is concerned particularly with methods and apparatus in'which the said oxidation is achieved by blowing or feeding an oxygen-containing gas into or onto a slowly flowing stream of molten crude metal or matte, through a succession of lances or tuyeres disposed along the path of flow of the molten material. It applies, for example, to the continuous refining of molten pig iron to steel and to the continuous conversion of copper or nickel mattes to copper and nickel respectively. In this specification the term metal includes crude metals, alloys and mattes, and each of the terms oxygen and oxygen-containing gas includes oxygen, air and other suitable oxygen-containing gases.
It is an object of this invention to achieve higher refining efiiciency than is obtained with other known refining processes.
In earlier attempts at continuous refining of molten crude metals or mattes the slag has been removed directly through a taphole in the Wall of the main refining chamber. With this arrangement and practice it is not easy to achieve low metal or matte losses in the outgoing slag. The principal contributing factors to this carryover of metal or matte, mainly in the form of fine prills or beads, are:
'(ii) In cases where the taph-ole was located near to the crude metal or matte entry end, the more viscous nature of the slag in this cooler region.
The methods and furnace designs covered by this present invention aim to reduce considerably the carryover of metal or matte prills while at the same time achieving high refining efiiciency.
The invention in one general form is a method of refining metals which comprises introducing unrefined metal into a refining chamber, flowing the metal through the refining chamber to an outlet, introducing oxygen into the refining chamber at a succession of points therealong, introducing fiuxing materials into the refining chamber, flowing slag into a slag settling chamber, discharging slag from the slag settling chamber, and discharging refined metal from the refining chamber outlet.
The invention in another general form is apparatus for refining metals which comprises a furnace having an elongated refining chamber, an inlet through which unrefined metal is admitted to the refining chamber, the metal being caused to flow slowly through the refining chamber, an outlet through which refined metal is discharged from the refining chamber, means for introducing oxygen into or onto the metal at a succession of points during its flow through the refining chamber, means for introducing fluxing materials into the refining chamber,
a slag settling chamber communicating with the refining chamber, slag being caused to flow from the refining chamber into the slag settling chamber, and a slag outlet in the slag settling chamber.
In the case of elements like carbon or sulphur the products of oxidation are mostly gaseous, for example, carbon monoxide or sulphur dioxide, and these gases bubble out of the bath to enter the gas exit stream. Most of the other products of oxidation need fluxing to enable them to enter the slag phase, and in this invention it is envisaged that the fluxing additions will be made at appropriate points along the length of flow of the metal, preferably including additions near the metal outflow end of the furnace, and that the slag formed will flow countercurrent to the metal in order to pass out of the slag settling chamber at some position remote from the metal taphole. In some forms of the invention both concurrent slag flow and countercurrent slag fl-ow relative to metal are achieved.
In this present invention, the fiuxing additions may be made either through lances or tuyeres or through separate ports in the furnace roof or walls.
The term lance in this specification includes a tube having one or more discharge outlets through which an oxygen-containing gas, such as air, oxygen, or oxygen enriched air and/or gaseous liquid or particulate solid fuel and/or fluxes or other additives are injected or fed into the furnace. The lance may or may not be fluid cooled.
The refractories used to line the furnace are appropriate to the reactants used and to the products formed in the furnace and to the temperature and other conditions existing in the furnace; for example in the refining of molten pig iron, high quality basic refractories rich in magnesium oxideare appropriate. In the refining of copper or nickel mattes, dense chrome-magnesite refractories are suitable. Alternatively in certain zones of the furnace, fluid cooled jackets may be used to form the Walls and/or roof of the furnace.
The slag settling chamber preferably comprises a branch of the furnace which communicates with the refining chamber, either at or near the metal inlet or at a point intermediate between the metal inlet and the metal outlet, and the said slag branch may be disposed in line with, at right angles to or parallel to, the refining chamber, the furnace design being thus linear, L-shaped, U- shaped, T-shaped or of other appropriate shape when viewed in plan.
The slag outlet is suitably arranged at or near the end of the slag settling branch remote from the junction of said branch with the refining chamber, and said outlet may comprise a taphole, overfiow lip or other approved discharge means.
The floor of the slag settling branch preferably slopes upwards from the region of the junction with the refining chamber towards the slag outlet, so that metal which enters the slag branch or which settles out from the slag in the slag branch flows back into the refining branch. The level of the floor of the slag branch at the entry end of the said branch is preferably located at or near the intended level of the metal in the refining chamber, and the slag outlet is preferably located above the intended level of the metal and just below the slag level.
A slag Wall or barrier is provided in the refining chamber at or near the metal outlet.
A gas ofltake or outlet is provided in the furnace for removal of exit gases, and is preferably located in the slag settling branch at or near the slag outlet to ensure flow of gases concurrently with the slag from the refining chamber towards the slag outlet.
The unrefined metal is fed continuously or semi-continuously to the inlet of the refining branch, the refined metal is tapped continuously or semi-continuously from the metal outlet, and slag is discharged continuously, semi-continuously or intermittently from the slag outlet.
In a further form of the invention simultaneous concurrent slag fiow and countercurrent slag flow are achieved by employing a T-shaped furnace having a slag branch which extends preferably at right angles to the refining chamber and is joined with said chamber at a point intermediate between the metal inlet and the metal outlet, for example, at a point about midway between said inlet and outlet. Slag is withdrawn from the end of the slag branch remote from the junction thereof wit-h the refining chamber. The floor of the slag branch slopes upwardly towards the slag outlet and for most or all of its length is above the level of the metal in the refining chamber.
In an alternative arrangement, the slag branch is disposed linearly relative to the refining chamber, that is, it extends substantially in line with the elongated refining chamber and communicates therewith at the entry or inlet end thereof. In another arrangement the slag branch is disposed substantially at right angles to the refining chamber and communicates with said chamber at or near its inlet end, thereby forming a substantially L-shaped furnace. In a still further arrangement the refining chamber and slag branch are arranged substantially parallel to one another and are connected by a common inlet section.
In all forms of the invention the provision of a raised and sloping floor in the slag branch or section of the furnace ensures that (a) little stirring action can take place between metal and slag because there is little reacting underlying metal in the slag branch or section, and (b) the beads or prills of metal which settle out from the slag in the slag branch are caused to gravitate back to the main refining chamber or section of the furnace.
Other features and variations of the invention will become apparent from the ensuing description of the forms of the invention illustrated in the accompanying drawings, wherein:
FIGURE 1 is a view in longitudinal elevation of a T-shaped furnace,
FIGURE 2 is a view in sectional plan of the furnace shown in FIGURE 1,
FIGURE 3 is a view in sectional transverse elevation taken on the line 33 of FIGURE 2,
FIGURE 4 is a semi-isometric view of a linear furnace,
FIGURE 5 is a view in sectional longitudinal elevation of the furnace shown in FIGURE 4,
FIGURE 6 is a view in sectional end elevation taken on the line 6-6 of FIGURE 5,
FIGURE 7 is a view in sectional plan of an L-shaped furnace, and
FIGURE 8 is a view in sectional plan of a U-shaped furnace.
Referring to the drawings, in which the same references are used to indicate like or corresponding parts or features, and with particular reference to FIGURES 1, 2 and 3, the main refining chamber 10 has a refractory floor 11, side walls 12 and arched roof 13, and a metal or matte entry or inlet 14 and a metal outlet 15. A slag barrier 16 is provided ahead of or near to the metal outlet 15.
A slag branch 18 having a floor 19, side walls 20 and roof 21 is connected at its inner or entry end 22 to the main refining chamber 10. The upper surface 23 of the fioor of slag branch 18 slopes upwardly from at or near the expected level of the metal or matte 24 in the chamber It) to above that level at the slag outlet 25. An auxil iary slag outlet 29 for testing purposes, may be provided. The slag branch 18 connects with the refining chamber 10 at about its centre and between the sections 10a and 10b of said chamber 14).
A gas off-take 26 is provided, either (as shown) through the roof 21 of the slag branch 18, or (not shown) through the end wall of the said branch 18. In some applications (not shown) the gas outlet may be located in the roof or walls of the refining chamber 10.
An oxygen-containing gas is introduced under pressure through lances 27 at successive points or intervals along the length of the main refining chamber 10. Alternatively, the oxygen-containing gas may be introduced through tuyeres (not shown) in a side wall 12 of the refining chamber 10. The number and size of the lances 27 or tuyeres are chosen to suit the type of material being treated and the design of the furnace employed. The oxygen-containing gas is injected into or onto the molten metal 24 in the refining chamber 10 and causes turbulence therein.
Fluxes, preferably in particulate form, may be introduced, through the lances 27 or tuyeres, in an entrained state in the oxygen-containing gas, or may be introduced separately through ports or lances (not shown) in the roof or sides of the refining chamber 10. The fiuxing material or materials is or are preferably introduced into the refining chamber 10 near to the metal inlet 14 and also near to the metal outlet 15. It would generally be less efiicient to add fiuxing material near to the centre of the refining chamber 10 and about opposite to the slag branch 18 which is designed to take away the slag 28 to the slag taphole or outlet 25, since if this were done there would be inadequate contact between the fiuxing chemicals and the bath containing the elements they are to remove. Another advantage of adding fiuxing materials near to the inlet 14 and near to the outlet 15 is that it ensures that there is ample flux to react with the first impurity oxides formed, namely SiO in the case of pig iron refining and FeO in matte converting, while the flux added near to the metal outlet 15 acts as a scavenger of fiuxable impurities. Usually the amount of fiuxing material added near the outlet 15 will be considerably less than that added near the inlet 14.
While the T-branched form of furnace shown in FIG- URES 1 to 3 is preferred for certain applications, the benefits of a separate slag settling branch 18, with its raised and sloping floor 19, and of sequential jetting of oxygen-containing gases in the refiner branch 10, can be achieved with other arrangements of the principal features. Thus, the slag branch 18 can be disposed so as to become a linear continuation of the refining chamber 10. An example of this form is shown in FIGURES 4, 5 and 6. Other arrangements or relationships of the refining chamber 10 and slag branch 18 are shown in plan in FIG- URES 7 and 8.
Referring to FIGURES 4 to 6, there is illustrated therein a linear form of furnace 31 of substantially circular cross-section which is set up on roll supports 32 so that the furance 31 may be tilted, when desired, either for the purpose of fettling the refractories or to repair a tuyere or to facilitate draining at the end of a furnace campaign. This particular form of furnace has been found to be particularly suitable for continuous conversion of mattes although, with minor modifications, it can also be used for other continuous refining operations, as for example the continuous production of steel from molten pig iron.
The matte or crude metal 24 is fed to the refining chamber 10 via a launder 33 and through the side or top opening 34 in the furnace 31. The matte or crude metal 24 then makes its way slowly along refining chamber 10 towards the metal outlet 15, the floor 35 of the refining chamber 10 being arranged to slope gently towards the said metal outlet 15. The metal 24 during its passage along the refining chamber 10 is vigorously stirred and reacted with successive jets of oxygen-containing gas which are injected from the tuyeres 36, into the matte or crude metal 24 in the bath. The oxygencontaining gas supply to the tuyeres 36 is supplied under pressure from tube 37 and if the gas is hot air this tube is well lagged.
Fluxes may be added, as in other forms of the invention, usually in particulate form, either entrained in the oxygen-containing gas and via the tuyeres 36, or through separate ports as, for example, those shown at 38 and 39 the fluxes being added through hoppers 41 connecting with said ports.
The slag 28 formed along the length of the refining section moves countercurrent to the matte or metal 24 on the surface of the metal 24 and passes into the slag settling section 18 and ultimately passes out of the furnace over the ridge or lip 42 and via taphole 25. Auxiliary slag outlets 45 and 46 may be provided for testing purposes.
The hot gases move generally in the same direction as the slag 28 and leave the furnace via gas off-take 26, which is conveniently located approximately centrally in the end wall of the slag branch 18; the stack position is therefore able to register with the ofi-take aperture 45a in the furnace 31 at all times, even when the furnace is tilted through an appreciable angle, as may be required occasionally during fettling or a tuyere repair.
In the application of this form of the invention to copper matte conversion it is advantageous to provide a well or sump 43 at the metal outlet end. This provides a reservoir for the metallic copper 44 which is forming continuously by the oxidation reactions with the white matte, Cu S. The copper 44 is tapped continuously or semi-continuously via the outlet 15. If desired, a small jet (not shown) of oxygen-containing gas may be directed at the copper as it is held or flows out of the outlet 15. This helps to remove much of the residual sulphur which may exist in the copper collected in the well or sump 43. With 'the same end in view, an oxygen-containing gas may be injected through a refractory tube (not shown) passed down the tapping spout into the well 43.
With continuous matte conversion it is often advantageous to add a little pyrites to the slag branch 18 at a position such as that of the port 40. The pyrites helps to wash out of the slag 28 very small prills of copper matte which may have been carried into the branch 13 in the slag 28. It also provides an extra source of heat in the slag branch 18 and additional sulphur dioxide. If it is desired to add oxidised ores or concentrates or dried cement copper, these may conveniently and advantageously be added at positions such as 38 or 39 together with silica flux.
In FIGURE 7 the slag branch 18 is more or less at right angles to the refining chamber 10. Matte or crude metal enters at inlet 14 in the corner region of the furnace, refined metal is withdrawn at 15, and slag is tapped at 25.
FIGURE 8 shows another arrangement of the slag branch 18 relative to the refining chamber 10. In this U- shaped furnace in which the slag branch 18 and refining chamber 10 are substantially parallel, the matte or crude metal is conveniently admitted via inlet 14 (e.g., a spout or small furnace branch) at the bend of the U, and re fined metal is withdrawn at outlet 15 and slag at outlet 25.
While the furnaces shown in FIGURES 7 and 8 are not ireadily tiltable, they have an advantage over the straight line arrangement shown in FIGURES 4 to 6 in that there is less tendency for splashes of matte or metal to be carried into the slag settling branch 18.
In each furnace arrangement, countercurrent fiow of slag relative to the metal is achieved, and metal which 7 enters or settles out in the slag branch is returned to the refining chamber, refined metal being withdrawn from the refining chamber and slag being withdrawn from the slag branch. In the furnace arrangement shown in FIG- URES 1 to 3, both concurrent flow and countercurrent flow of slag relative to metal are achieved, the former occurring in the section 10a of the chamber 10 and the latter occurring in the section 10b of said chamber, and the slag enters the slag branch 18 from both the section 10a and the section 1012.
Reference will now be made to the application of the invention to the continuous refining to steel of molten pig iron or of semi-steel, from whatever production source, and containing silicon, phosphorus and sulphur as impurities, as well as carbon. The description applies particularly to the T-branched form of furnace shown in FIGURES 1 to 3 but those familiar with the art will readily appreciate how, with minor modifications, the refining can be carried out in other furnace shapes covered by this invention.
The flux additions are either particulate limestone or burnt lime. The limestone or lime added through or close to the lance or lances 27 nearest to the entry end 14 is immediately available to flux the silica formed by the oxidation of the readily oxidisable silicon in the bath metal 24. At the entry end of the refining chamber the slag has the lowest basicity, as measured by the CaO/SiO ratio. On the other hand, the limestone or lime added or blown in near to the exit end 15 has little or no silica to flux and so a high basicity is established and maintained. This high basicity is associated with a high degree of oxidation, the slag here containing a significant proportion of ferritic ions. These conditions, combined with the stirring of metal and slag by the jetting action and the gentle carbon boiling action (mainly CO evolution), ensures a high refining efiiciency with respect to sulphur and phosphorus.
As the slag formed in the section 10b of the furnace flows countercurrent to the steel bath underneath it, its composition progressively changes, giving back to the metal bath much of its iron content but retaining its sulphur and phosphorus. Finally, as indicated by the arrow 2812, it blends with the somewhat lower basicity concurrent-flow slag stream from the section 10a of the furnace (indicated by the arrow 28a) to flow out into the slag branch 18; Until this point, both the concurrent slag stream 28a and the countercurrent slag stream 28b have been subjected to active mixing with the metal, because of the aforementioned jetting actions of the oxygen-containing gas and the boiling resulting from the liberation of carbon monoxide from the progressively refined metal bath. Once the slag streams enter the slag branch 18, however, this vigorous stirring action substantially ceases, because, as has previously been explained, the fioor level 23 of the branch 18 is at or above the level of the metal 24 in the main refining chamber 10. These more quiescent conditions in the slag branch 1.8 ensure that any prills or beads of metal carried in the slag 28 will have opportunity to settle down to the floor of branch 18 and as the said floor is sloped gently towards the refining chamber 10, such metal rejoins the metal in the main bath.
It is, ofcourse, necessary to maintain an appropriate temperature in the slag 28 within the slag branch 18. The location of the gas off-take 26 towards the end of the branch 18 contributes materially to that end. The hot carbon monoxide-rich gases leaving the main refining chamber 10 radiate heat down onto the slag surface. If it should prove necessary to increase the temperature of these exit gases over the slag branch 18 a little oxygen can be injected through a turbulent jet through a small port (not shown) at a point in the branch 18, preferably .near to the main refining chamber 10. This auxiliary oxygen leads to combustionof some of the carbon monoxide in the outgoing gases and gives a corresponding rise in temperature.
The location of the gas off-take 26 in or on the branch 18 rather than in the roof of the main refining chamber 10 also simplifies the roof design of the latter and permits freer access by crane to the whole length of the roof in the refining chamber 10. This is of importance when it is desired to make rapid replacement of a burnt-out section of the roof or to effect other repairs to the top of the furnace.
In the application to matte refining, it is highly desirable that the oxidation conditions in the refining branch be controlled so that the iron passes mostly into the ferrous condition, FeO, and thence to the slag as 2FeO.SiO or its equivalent, rather than to magnetite, Fe O Magnetite is not readily fiuxed by silica at normal operating temperatures. Should magnetite form to an undesirable degree and build up on the walls or end bafiles, the accretions can usually be removed by raising the temperature locally and particularly by firing, via a lance, a mixture of pyrites concentrates and sand at the accreted region. As the exothermic oxidation of pyrite raises the temperature, above 1280 C., a reaction of the type:
sets in and takes the iron oxide into solution in the slag. The necessary localised rise in temperature can also be achieved by lancing with an oxy-fuel burner.
In the refining of nickel-iron sulphides, difficulties may develop if the conditions in the outlet end of the refining chamber are allowed to become too quiescent and oxidising. This is because of the tendency to form refractory layers of nickel oxide and nickel. These tend to retard or even stop further refining action. These difiiculties can be avoided by (a) ensuring that vigorous turbulence is maintained in the refining zone, as by jetting with gas, and (b) incorporating a little fine coal or other hydrocarbon with the oxygen-containing gas blown into the final refining zone. It will be appreciated that nickel, having a much higher melting point than copper, must be produced at temperatures 300400 C. higher than those of the reactions necessary to refine copper matte to blister copper. It will also be appreciated that this invention is applicable to the conversion of mixed sulphide mattes, as for example copper-nickel mattes, to produce alloys, for example cupro-nickels.
In all forms of the invention, the heat in the exit gases may be used for preheating air or other oxygen-containing gas or for steam raising or for other purposes. In the case of continuous matte refining, the exit gases contain a sufficiently high tenor of sulphur dioxide to make them well suited to acid manufacture. In the application to pigiron refining, the exit gases not only carry much sensible heat but may also contain appreciable chemical heat in the form of unburnt carbon monoxide, and the combined heat value can be utilised in various ways.
The following examples illustrate the invention:
Example 1 Continuous refining of molten pig iron to steel was effected in a furnace similar to that shown in FIGURES 1, 2 and 3. Hot metal at 1290 C.:15 C. and containing 4.1% C, 0.95% Si, 0.76% Mn, 0.12% P, and 0.05% S was fed from an oil-fired tilting ladle at the rate of 4 tons per hour into entry end 14 of the refining chamber and was subjected to successive jetting with 99.5% oxygen from five lances 27. Powdered burnt lime was added via small roof ports near to the first and last lances 27, thus developing both concurrent and countercurrent slag fiow over the bath metal. Steel was tapped from outlet at 1590 0:20 C. and contained 0.35% C, 0.005% Si, 0.12% Mn, 0.012% P and 0.023% S. The slag tapped from the slag branch 18 at outlet 25 had a ratio of 1.4 and contained 11% to 13% FeO with less than 0.5% metallic iron in the form of prills.
To illustrate the benefit of the slag branch 18 with its sloping floor and of the practice of concurrent-countercurrent slag flow, some samples of steel and slag were taken when:
(a) Lime was added only at the entry end 14 of the refiner chamber 10, and
(b) Slag was tapped through an auxiliary taphole 29 in the furnace wall located just before the taphole 15.
8 In this case the steel contained 0.39% C, 0.005% Si, 0.18% Mn, 0.06% P and 0.04% S while the slag contained 19% total iron of which between 4% and 6.5% was in the form of prills of steel.
Example 2 Continuous conversion of copper matte: Matte of the following composition, Cu 41.2%, Fe 20.1%, S 24.8%, was raised to 1250 C. in an auxiliary oil-fired tilting furnace and poured at a steady rate of 2 tons per hour into the middle entry port 34 of a straight line furnace of the type shown in FIGURES 4 to 6. On refining by jetting with a 50:50 mixture of air and 99.5% oxygen and using silica sand as flux, copper containing 99.0% Cu and 0.85% S was tapped at the outlet spout 15, while the slag tapped at outlet 25, after settling in a slag branch 18, five feet long with sloping bottom, contained 0.65% Cu, most of this being in the for-m of very fine prills of white matte. By contrast, slag tapped from slag branch of the same furnace but from an auxiliary taphole 45 (see FIGURE 5) located in the side wall at a position about 9 inches away from the refiner section 10, contained between 1.8 and 3.6% copper, some of which was in the form of prills visible to the naked eye. Slag tapped from another auxiliary taphole 46 (see FIGURE 5) at the inlet end of the refining chamber 10 contained between 4% and 6% copper.
The addition of a little pyrites to the slag branch 18 at position 40 (see FIGURE 5) lowered the copper in the slag from the outlet 25 to below 0.5%.
I claim:
1. A method of refining metals which comprises the steps of: introducing unrefined metal into the refining chamber of a refining furnace, flowing the metal through the refining chamber to a metal outlet, injecting oxygencontaining gas into the flowing metal in the refining chamber during the fiow of metal therethrough; maintaining turbulent agitation in the molten metal in the refining chamber by the injection of the oxygen-containing gas; inducing flow of slag countercurrently to the flow of metal in at least a part of the refining chamber; flowing the slag formed in the refining chamber into a slag separation chamber which communicates with the refining chamber; maintaining substantially quiescent conditions in the slag separation chamber; discharging slag from a slag outlet in the slag separation chamber; and discharging refined metal from the metal outlet.
2. A method according to claim 1 wherein in one part of the refining chamber slag is flowed concurrent to the fiow of metal and in another part of the refining chamber slag is flowed countercurrent to the flow of metal.
3. A method according to claim 1 wherein the slag separation chamber connects with the refining chamber at a point between the metal inlet and the metal outlet; and wherein slag flows concurrent to the metal in the part of the refining chamber between the metal inlet and the entry to the slag separation chamber and flows countercurrent to the metal in the part of the refining chamber between the entry to the slag separation chamber and the metal outlet.
4. A method according to claim 1 wherein the oxygencontaining gas is injected into the molten material in the refining chamber at an angle to the surface thereof and in the direction of flow of the slag.
5. A method according to claim 1 wherein the oxygencontaining gas is injected into the molten material in the refining chamber at a succession of points along the refining chamber.
6. A method according to claim 1 wherein metal which settles from the slag in the slag separation chamber flows under gravity back into the refining chamber.
7. A method according to claim 1 wherein the level of the floor of the slag separation chamber is generally above the intended level of the metal in the refining chamber and said floor slopes upwardly away from the refining chamber.
8. A method according to claim 1 wherein the slag separation chamber has a slag entry and a slag outlet, and the floor of the slag separation chamber slopes upwardly from the slag entry towards the slag outlet.
9. A method according to claim 1 wherein the floor of the refining chamber slopes downwardly towards the metal outlet.
10. A method according to claim 9 wherein the floor of the refining chamber slopes downwardly towards a metal reservoir, and metal flows from the refining chamber through said reservoir to the metal outlet.
11. A method according to claim 1 wherein the slag separation chamber extends substantially at right angles to'the refining chamber.
12. A method according to claim 1 wherein the slag separation chamber and the refining chamber are substantially parallel.
References Cited UNITED STATES PATENTS Garretson 266-11 X Fowler 7572 Simpson 75-92 X Gronningsalter 75-89 X Gilliland 75-65 X Sittner 266-37 Gilliland 75-40 Jordan 75-46 Perrin 266-37 Alexandrovsky 75-46 X Huntington 75-46 X Johnson 75-24 Zimmerley 75- 65 X Gray 75-24 DAVID L. RECK, Primary Examiner. 20 H. W. TARRING, Assistant Examiner.
Claims (1)
1. A METHOD OF REFINING METALS WHICH COMPRISES THE STEPS OF: INTRODUCING UNREFINED METAL INTO THE REFINING CHAMBER OF A REFINING FURNACE, FLOWING THE METAL THROUGH THE REFINING A CHAMBER TO A METAL OUTLET, INJECTING OXYGENCONTAINING GAS INTO THE FLOWING METAL IN THE REFINING CHAMBER DURING THE FLOW OF METAL THERETHROUGH; MAINTAINING TURBULENT AGITATION IN THE MOLTEN METAL IN THE REFINING CHAMBER BY THE INJECTION OF THE OXYGEN-CONTAINING GAS; INDUCING FLOW OF SLAG COUNTERCURRENTLY TO THE FLOW OF METAL IN AT LEAST A PART OF THE REFINING CHAMBER; FLOWING THE SLAG FORMED IN THE REFINING CHAMBER INTO A SLAG SEPARATION CHAMBER WHICH COMMUNICATES WITH THE REFINING CHAMBER; MAINTAINING SUBSTANTIALLY QUIESCENT CONDITIONS IN THE SLAG SEPARATION CHAMBER; DISCHARGING SLAG FROM A SLAG OUTLET IN THE SLAG SEPARATION CHAMBER; AND DISCHARGING REFINED METAL FROM THE METAL OUTLET.
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU27676/63A AU273494B2 (en) | 1963-02-21 | Continuous production of furnace products | |
AU29505/63A AU281236B2 (en) | 1963-04-11 | Direct smelting of metallic ores and concentrates | |
AU3039263 | 1963-05-07 | ||
AU3473863 | 1963-08-28 | ||
AU3803463 | 1963-11-25 | ||
AU4124464 | 1964-02-24 | ||
US570270A US3326671A (en) | 1963-02-21 | 1966-08-04 | Direct smelting of metallic ores |
US61910867A | 1967-01-05 | 1967-01-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3326672A true US3326672A (en) | 1967-06-20 |
Family
ID=27570041
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US345987A Expired - Lifetime US3288451A (en) | 1963-02-21 | 1964-02-19 | Continuous production of furnace products |
US390042A Expired - Lifetime US3326672A (en) | 1963-02-21 | 1964-08-17 | Refining of metals and alloys |
US619108A Expired - Lifetime US3463472A (en) | 1963-02-21 | 1967-01-05 | Apparatus for the direct smelting of metallic ores |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US345987A Expired - Lifetime US3288451A (en) | 1963-02-21 | 1964-02-19 | Continuous production of furnace products |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US619108A Expired - Lifetime US3463472A (en) | 1963-02-21 | 1967-01-05 | Apparatus for the direct smelting of metallic ores |
Country Status (12)
Country | Link |
---|---|
US (3) | US3288451A (en) |
AT (1) | AT266461B (en) |
BE (3) | BE644174A (en) |
DE (2) | DE1519752A1 (en) |
FI (1) | FI43791C (en) |
FR (3) | FR1387509A (en) |
GB (3) | GB1003026A (en) |
LU (1) | LU45859A1 (en) |
MY (1) | MY7000089A (en) |
NL (1) | NL6403867A (en) |
SE (2) | SE304581B (en) |
YU (1) | YU31189B (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3427150A (en) * | 1965-08-19 | 1969-02-11 | Niehaus Eng Sa | Process for manufacturing iron or steel with low sulphur content |
US3432289A (en) * | 1966-03-23 | 1969-03-11 | Milton I Schwab | Method of refining copper |
US3514280A (en) * | 1967-10-19 | 1970-05-26 | Sherwood William L | Continuous steelmaking method |
DE1800131B1 (en) * | 1968-10-01 | 1971-05-27 | Conzinc Riotinto Ltd | Multi-zone melting process and multi-zone melting furnace for the continuous production of steel |
FR2083585A1 (en) * | 1970-03-26 | 1971-12-17 | Kaiser Aluminium Chem Corp | |
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 |
US3791816A (en) * | 1972-03-30 | 1974-02-12 | Kaiser Aluminium Chem Corp | Production of nickel from nickel-bearing materials |
US3865579A (en) * | 1970-01-05 | 1975-02-11 | Koppers Co Inc | Method and apparatus for the production of steel |
US3941587A (en) * | 1973-05-03 | 1976-03-02 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3980283A (en) * | 1971-02-16 | 1976-09-14 | Gesellschaft Zur Forderung Der Eisenhuttentechnik Mbh | Apparatus for performing a continuous metallurgical refining process |
US3988148A (en) * | 1973-05-03 | 1976-10-26 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3988149A (en) * | 1973-05-03 | 1976-10-26 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3990889A (en) * | 1973-05-03 | 1976-11-09 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3990890A (en) * | 1972-05-17 | 1976-11-09 | Creusot-Loire | Process for refining molten copper matte with an enriched oxygen blow |
US4115108A (en) * | 1975-12-04 | 1978-09-19 | Elkem-Spigerverket A/S | Matte smelting |
US4252560A (en) * | 1978-11-21 | 1981-02-24 | Vanjukov Andrei V | Pyrometallurgical method for processing heavy nonferrous metal raw materials |
US4294433A (en) * | 1978-11-21 | 1981-10-13 | Vanjukov Andrei V | Pyrometallurgical method and furnace for processing heavy nonferrous metal raw materials |
US4478394A (en) * | 1980-04-16 | 1984-10-23 | Outokumpu Oy | Apparatus for the separation of lead from a sulfidic concentrate |
EP0171845A1 (en) * | 1984-08-16 | 1986-02-19 | Norddeutsche Affinerie Ag | Process and apparatus for the continuous pyrometallurgical treatment of a copper-lead matte |
US5284812A (en) * | 1992-01-06 | 1994-02-08 | Minnesota Mining And Manufacturing Company | Thiazolo[5,4-d]thiazole color-formers |
US5374298A (en) * | 1990-11-20 | 1994-12-20 | Mitsubishi Materials Corporation | Copper smelting process |
US5733358A (en) * | 1994-12-20 | 1998-03-31 | Usx Corporation And Praxair Technology, Inc. | Process and apparatus for the manufacture of steel from iron carbide |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1130255A (en) * | 1965-11-22 | 1968-10-16 | Conzinc Riotinto Ltd | Reverberatory smelting of copper concentrates |
FR1502663A (en) * | 1966-05-17 | 1967-11-24 | Saint Gobain | Glass manufacturing process |
US3473918A (en) * | 1966-06-17 | 1969-10-21 | Anaconda Co | Production of copper |
US3617042A (en) * | 1967-08-14 | 1971-11-02 | Nat Res Inst Metals | Apparatus for continuous refining of molten metals |
AU421598B2 (en) * | 1968-03-29 | 1972-02-21 | Monzino Riotinto Of Australia Limited | Separation of molten materials |
DE1758537B1 (en) * | 1968-06-22 | 1973-03-22 | Salzgitter Peine Stahlwerke | METHOD AND DEVICE FOR CONTINUOUS REFRESHING OF BIG IRON TO STEEL |
US3554519A (en) * | 1968-09-09 | 1971-01-12 | United States Steel Corp | Furnace for producing steel continuously |
CA934968A (en) * | 1970-03-20 | 1973-10-09 | C. Liang Shou | Lead smelting process |
CA938111A (en) * | 1970-03-26 | 1973-12-11 | E. Mahin William | Production of metals from metalliferous materials |
US4006003A (en) * | 1975-10-29 | 1977-02-01 | Owens-Illinois, Inc. | Process for melting glass |
US4180251A (en) * | 1977-03-25 | 1979-12-25 | Dravo Corporation | Apparatus for recovering lead from battery mud |
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 |
US4249722A (en) * | 1979-05-11 | 1981-02-10 | Dravo Corporation | Apparatus for the flash oxidation of metal concentrates |
US4389243A (en) * | 1979-05-11 | 1983-06-21 | Dravo Corporation | Method for the flash oxidation of metal concentrates |
JPS57188427A (en) * | 1981-01-23 | 1982-11-19 | Bethlehem Steel Corp | Mineral wool and manufacture |
DE3304504A1 (en) * | 1983-02-10 | 1984-08-16 | Metallgesellschaft Ag, 6000 Frankfurt | METHOD FOR CONTINUOUSLY MELTING IRON SPONGE |
US4472195A (en) * | 1983-08-15 | 1984-09-18 | Olin Corporation | Process for decarburizing alloy melts |
US4632687A (en) * | 1985-06-25 | 1986-12-30 | Ppg Industries, Inc. | Method of melting raw materials for glass or the like using solid fuels or fuel-batch mixtures |
US4701217A (en) * | 1986-11-06 | 1987-10-20 | University Of Birmingham | Smelting reduction |
US5223234A (en) * | 1988-12-22 | 1993-06-29 | Kloeckner-Humboldt-Deutz Ag | Method for producing molybdenum trioxide (MOO3) from raw materials that contain MOS2 |
US5060913A (en) * | 1989-08-30 | 1991-10-29 | Regents Of The University Of Minnesota | Integrated metallurgical reactor |
US5069715A (en) * | 1990-04-02 | 1991-12-03 | Regents Of The University Of Minnesota | Direct smelting process and apparatus |
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 |
US5258054A (en) * | 1991-11-06 | 1993-11-02 | Ebenfelt Li W | Method for continuously producing steel or semi-steel |
US5558696A (en) * | 1993-12-15 | 1996-09-24 | Bechtel Group, Inc. | Method of direct steel making from liquid iron |
US5429658A (en) * | 1992-10-06 | 1995-07-04 | Bechtel Group, Inc. | Method of making iron from oily steel and iron ferrous waste |
AUPP570098A0 (en) | 1998-09-04 | 1998-10-01 | Technological Resources Pty Limited | A direct smelting process |
AUPQ152299A0 (en) | 1999-07-09 | 1999-08-05 | Technological Resources Pty Limited | Start-up procedure for direct smelting process |
DE102004049234B4 (en) * | 2004-10-09 | 2011-06-09 | Xstrata Technology Pty Ltd. | Process for recovering pure copper |
GB0608080D0 (en) * | 2006-04-25 | 2006-05-31 | Warner Noel A | Co-production of steel, titanium and high-grade oxide |
CN100535133C (en) * | 2006-12-30 | 2009-09-02 | 李继宗 | Steel making lime additive and its production process |
US20100107820A1 (en) * | 2008-11-04 | 2010-05-06 | Euston Charles R | Method for drying copper sulfide concentrates |
US11492281B2 (en) * | 2017-06-28 | 2022-11-08 | Corning Incorporated | Melters for glass forming apparatuses |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US596991A (en) * | 1898-01-11 | g-abretson | ||
US1822588A (en) * | 1929-01-14 | 1931-09-08 | United Verde Copper Company | Recovering copper from slags |
US1940977A (en) * | 1932-03-08 | 1933-12-26 | Internat Chromium Process Corp | Metallurgical process and apparatus |
US2426607A (en) * | 1945-04-21 | 1947-09-02 | Falconbridge Nickel Mines Ltd | Production of metals |
US2526473A (en) * | 1950-10-17 | giu-iland | ||
US2550502A (en) * | 1948-01-30 | 1951-04-24 | Gen Electric | Apparatus for purifying metals |
US2557650A (en) * | 1948-07-30 | 1951-06-19 | Standard Oil Dev Co | Metallurgical process |
US2639984A (en) * | 1952-08-07 | 1953-05-26 | Jordan James Fernando | Continuous cupola-bessemer process |
US2718389A (en) * | 1950-11-17 | 1955-09-20 | Electro Chimie Metal | Skimmer for holding slag back during pouring metal |
US2862810A (en) * | 1950-02-02 | 1958-12-02 | Alexandrovsky Georges | Process and apparatus for reducing the silicon content and increasing the temperature of molten pig iron |
US3022157A (en) * | 1959-05-21 | 1962-02-20 | Pyromet Corp | Method for continuous hearth refining of steel and beneficiation of ores of ferro alloys |
US3091524A (en) * | 1959-10-23 | 1963-05-28 | Strategic Materials Corp | Metallurgical process |
US3102806A (en) * | 1958-06-10 | 1963-09-03 | Kennecott Copper Corp | Reverberatory smelting method and apparatus |
US3171735A (en) * | 1960-07-06 | 1965-03-02 | Metallurgical Processes Ltd | Treatment of arsenical drosses |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US596992A (en) * | 1898-01-11 | Xmethod o of and apparatus for-bgssemerizinq matte | ||
US1803663A (en) * | 1926-04-06 | 1931-05-05 | Carson Invest Company | Method and means for producing blister copper from copper bearing materials |
US1815946A (en) * | 1928-04-19 | 1931-07-28 | Langer Arthur | Extracting of iron |
US1911379A (en) * | 1930-01-03 | 1933-05-30 | Marx Peter | Cupola furnace |
US2161180A (en) * | 1936-04-27 | 1939-06-06 | Marx Peter | Apparatus for melting metals |
US2161181A (en) * | 1936-11-12 | 1939-06-06 | Marx Peter | Melting furnace |
US2451582A (en) * | 1941-09-09 | 1948-10-19 | American Rock Wool Corp | Apparatus for producing mineral wool |
US2603476A (en) * | 1949-09-17 | 1952-07-15 | Howard C Whiston | Circular open hearth melting furnace |
US2750277A (en) * | 1951-05-14 | 1956-06-12 | Armco Steel Corp | Process and apparatus for reducing and smelting iron |
US2689433A (en) * | 1952-05-12 | 1954-09-21 | Phoenix Glass Company | Glass melting tank |
US2872175A (en) * | 1955-02-14 | 1959-02-03 | Cie De Pont A Mousson | Annealing furnace |
FR1238667A (en) * | 1959-10-15 | 1960-08-12 | Process for obtaining a metallic product, in particular iron or steel, furnace for carrying out this process, or similar processes | |
US3214264A (en) * | 1959-10-23 | 1965-10-26 | Huettenwerk Oberhausen Ag | Treatment of metal oxides |
US3215424A (en) * | 1960-12-07 | 1965-11-02 | Kanamori Kuro | Apparatus for refining iron |
US3140168A (en) * | 1961-05-31 | 1964-07-07 | Inland Steel Co | Reduction of iron ore with hydrogen |
US3326671A (en) * | 1963-02-21 | 1967-06-20 | Howard K Worner | Direct smelting of metallic ores |
US3287006A (en) * | 1963-04-08 | 1966-11-22 | Yawata Iron & Steel Co | Continuous steel making furnace |
-
1964
- 1964-02-17 GB GB6523/64A patent/GB1003026A/en not_active Expired
- 1964-02-19 SE SE2015/64A patent/SE304581B/xx unknown
- 1964-02-19 US US345987A patent/US3288451A/en not_active Expired - Lifetime
- 1964-02-20 DE DE19641519752 patent/DE1519752A1/en active Pending
- 1964-02-21 BE BE644174D patent/BE644174A/xx unknown
- 1964-02-21 FR FR964764A patent/FR1387509A/en not_active Expired
- 1964-04-09 GB GB14818/64A patent/GB1055935A/en not_active Expired
- 1964-04-09 AT AT309464A patent/AT266461B/en active
- 1964-04-10 NL NL6403867A patent/NL6403867A/xx unknown
- 1964-04-10 SE SE4457/64A patent/SE315741B/xx unknown
- 1964-04-10 FI FI640758A patent/FI43791C/en active
- 1964-04-10 YU YU498/64A patent/YU31189B/en unknown
- 1964-04-10 BE BE646429A patent/BE646429A/xx unknown
- 1964-04-11 LU LU45859D patent/LU45859A1/xx unknown
- 1964-04-11 FR FR970642A patent/FR1429265A/en not_active Expired
- 1964-08-17 US US390042A patent/US3326672A/en not_active Expired - Lifetime
- 1964-08-18 DE DE19641458306 patent/DE1458306B2/en active Pending
- 1964-08-21 GB GB34235/64A patent/GB1064826A/en not_active Expired
- 1964-08-27 FR FR986427A patent/FR1405775A/en not_active Expired
- 1964-08-28 BE BE652436D patent/BE652436A/xx unknown
-
1967
- 1967-01-05 US US619108A patent/US3463472A/en not_active Expired - Lifetime
-
1970
- 1970-12-31 MY MY197089A patent/MY7000089A/en unknown
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US596991A (en) * | 1898-01-11 | g-abretson | ||
US2526473A (en) * | 1950-10-17 | giu-iland | ||
US1822588A (en) * | 1929-01-14 | 1931-09-08 | United Verde Copper Company | Recovering copper from slags |
US1940977A (en) * | 1932-03-08 | 1933-12-26 | Internat Chromium Process Corp | Metallurgical process and apparatus |
US2426607A (en) * | 1945-04-21 | 1947-09-02 | Falconbridge Nickel Mines Ltd | Production of metals |
US2550502A (en) * | 1948-01-30 | 1951-04-24 | Gen Electric | Apparatus for purifying metals |
US2557650A (en) * | 1948-07-30 | 1951-06-19 | Standard Oil Dev Co | Metallurgical process |
US2862810A (en) * | 1950-02-02 | 1958-12-02 | Alexandrovsky Georges | Process and apparatus for reducing the silicon content and increasing the temperature of molten pig iron |
US2718389A (en) * | 1950-11-17 | 1955-09-20 | Electro Chimie Metal | Skimmer for holding slag back during pouring metal |
US2639984A (en) * | 1952-08-07 | 1953-05-26 | Jordan James Fernando | Continuous cupola-bessemer process |
US3102806A (en) * | 1958-06-10 | 1963-09-03 | Kennecott Copper Corp | Reverberatory smelting method and apparatus |
US3022157A (en) * | 1959-05-21 | 1962-02-20 | Pyromet Corp | Method for continuous hearth refining of steel and beneficiation of ores of ferro alloys |
US3091524A (en) * | 1959-10-23 | 1963-05-28 | Strategic Materials Corp | Metallurgical process |
US3171735A (en) * | 1960-07-06 | 1965-03-02 | Metallurgical Processes Ltd | Treatment of arsenical drosses |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3427150A (en) * | 1965-08-19 | 1969-02-11 | Niehaus Eng Sa | Process for manufacturing iron or steel with low sulphur content |
US3432289A (en) * | 1966-03-23 | 1969-03-11 | Milton I Schwab | Method of refining copper |
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 |
DE1800131B1 (en) * | 1968-10-01 | 1971-05-27 | Conzinc Riotinto Ltd | Multi-zone melting process and multi-zone melting furnace for the continuous production of steel |
US3725044A (en) * | 1968-12-07 | 1973-04-03 | Mitsubishi Metal Corp | Method of continuous processing of sulfide ores |
US3865579A (en) * | 1970-01-05 | 1975-02-11 | Koppers Co Inc | Method and apparatus for the production of steel |
FR2083585A1 (en) * | 1970-03-26 | 1971-12-17 | Kaiser Aluminium Chem Corp | |
US3980283A (en) * | 1971-02-16 | 1976-09-14 | Gesellschaft Zur Forderung Der Eisenhuttentechnik Mbh | Apparatus for performing a continuous metallurgical refining process |
US3791816A (en) * | 1972-03-30 | 1974-02-12 | Kaiser Aluminium Chem Corp | Production of nickel from nickel-bearing materials |
US3990890A (en) * | 1972-05-17 | 1976-11-09 | Creusot-Loire | Process for refining molten copper matte with an enriched oxygen blow |
US3988149A (en) * | 1973-05-03 | 1976-10-26 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3988148A (en) * | 1973-05-03 | 1976-10-26 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3990889A (en) * | 1973-05-03 | 1976-11-09 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US3941587A (en) * | 1973-05-03 | 1976-03-02 | Q-S Oxygen Processes, Inc. | Metallurgical process using oxygen |
US4085923A (en) * | 1973-05-03 | 1978-04-25 | Q-S Oxygen Processes, Inc. | Apparatus for a metallurgical process using oxygen |
US4115108A (en) * | 1975-12-04 | 1978-09-19 | Elkem-Spigerverket A/S | Matte smelting |
US4294433A (en) * | 1978-11-21 | 1981-10-13 | Vanjukov Andrei V | Pyrometallurgical method and furnace for processing heavy nonferrous metal raw materials |
US4252560A (en) * | 1978-11-21 | 1981-02-24 | Vanjukov Andrei V | Pyrometallurgical method for processing heavy nonferrous metal raw materials |
US4478394A (en) * | 1980-04-16 | 1984-10-23 | Outokumpu Oy | Apparatus for the separation of lead from a sulfidic concentrate |
EP0171845A1 (en) * | 1984-08-16 | 1986-02-19 | Norddeutsche Affinerie Ag | Process and apparatus for the continuous pyrometallurgical treatment of a copper-lead matte |
US5374298A (en) * | 1990-11-20 | 1994-12-20 | Mitsubishi Materials Corporation | Copper smelting process |
US5284812A (en) * | 1992-01-06 | 1994-02-08 | Minnesota Mining And Manufacturing Company | Thiazolo[5,4-d]thiazole color-formers |
US5350857A (en) * | 1992-01-06 | 1994-09-27 | Minnesota Mining And Manufacturing Company | Thiazolo[5,4-D]thiazsole Color-formers |
US5733358A (en) * | 1994-12-20 | 1998-03-31 | Usx Corporation And Praxair Technology, Inc. | Process and apparatus for the manufacture of steel from iron carbide |
Also Published As
Publication number | Publication date |
---|---|
DE1458306B2 (en) | 1971-09-02 |
BE644174A (en) | 1964-06-15 |
BE646429A (en) | 1964-10-12 |
DE1458306A1 (en) | 1969-02-20 |
BE652436A (en) | 1964-12-16 |
US3288451A (en) | 1966-11-29 |
LU45859A1 (en) | 1965-10-11 |
DE1519752A1 (en) | 1970-02-26 |
FR1387509A (en) | 1965-01-29 |
GB1064826A (en) | 1967-04-12 |
SE304581B (en) | 1968-09-30 |
YU31189B (en) | 1973-02-28 |
FI43791B (en) | 1971-03-01 |
FR1429265A (en) | 1966-02-25 |
NL6403867A (en) | 1964-10-12 |
FR1405775A (en) | 1965-07-09 |
AT266461B (en) | 1968-11-25 |
MY7000089A (en) | 1970-12-31 |
FI43791C (en) | 1971-06-10 |
US3463472A (en) | 1969-08-26 |
GB1003026A (en) | 1965-09-02 |
SE315741B (en) | 1969-10-06 |
GB1055935A (en) | 1967-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3326672A (en) | Refining of metals and alloys | |
US3326671A (en) | Direct smelting of metallic ores | |
US4085923A (en) | Apparatus for a metallurgical process using oxygen | |
US4457777A (en) | Steelmaking | |
US9499872B2 (en) | Iron reduction process and equipment | |
US3912501A (en) | Method for the production of iron and steel | |
US3634065A (en) | Method for refining metals | |
WO1997020954A1 (en) | Simplified duplex processing of nickel ores and/or concentrates for the production of ferronickels, nickel irons and stainless steels | |
US4294433A (en) | Pyrometallurgical method and furnace for processing heavy nonferrous metal raw materials | |
RU2346056C2 (en) | Method of steel direct production from iron-bearing materials | |
US4052197A (en) | Process for making steel from pig iron | |
US7749301B2 (en) | Process for copper converting | |
US3473918A (en) | Production of copper | |
US3752663A (en) | Continuous production of liquid steel using arc furnaces | |
US3022157A (en) | Method for continuous hearth refining of steel and beneficiation of ores of ferro alloys | |
US3988148A (en) | Metallurgical process using oxygen | |
US3432157A (en) | Apparatus for refining metals | |
US5885325A (en) | Process and apparatus for the manufacture of steel | |
US3990889A (en) | Metallurgical process using oxygen | |
US5733358A (en) | Process and apparatus for the manufacture of steel from iron carbide | |
US693062A (en) | Manufacture of pig-iron. | |
WO1997020958A1 (en) | Recovery of cobalt from slag | |
RU2548871C2 (en) | Method for direct production of metals from materials containing iron oxides (versions) and device for implementing it | |
Pehlke | An overview of contemporary steelmaking processes | |
Fruehan | Evaluation of steelmaking processes |