US1717160A - Reduction of complex ores - Google Patents
Reduction of complex ores Download PDFInfo
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- US1717160A US1717160A US753810A US75381024A US1717160A US 1717160 A US1717160 A US 1717160A US 753810 A US753810 A US 753810A US 75381024 A US75381024 A US 75381024A US 1717160 A US1717160 A US 1717160A
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- Prior art keywords
- reduction
- ore
- iron
- nickel
- chromium
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- 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
- C22B23/005—Preliminary treatment of ores, e.g. by roasting or by the Krupp-Renn process
Definitions
- This invention relates to a process for the reduction of complexores whereby the metallic components of the ore can be recovered and substantially separated. It relates more 5 particularly to an iron ore having, associated therewith reducible com ounds of other metals asfor example, oxi es, some of which other metals it may be desired to alloy with a of further metallic components of the ore, re-
- a particular ore which is amenable to treatment by. my process is the Mayari' iron ore of Cuba, said ore being mainly a limonite associllligd with chromite, and containing apao proxi tely 2.00% chromium, .7 5% nickel and 0.6% manganese. 1
- This ore also contains a high percentage of moisture, which on removal leaves a product, mainly in a state of fine subdivision, unsuitable for a blast furglomerating process .is
- the blast fur- 40 nace product is a chromiferous pig iron, containi approximately 2% of chromium and 1% o nic e].
- the chromium ma be sucvcessfu'll removed from this chromi erous pig iron by inerizing processes known to the art and the. dechromized iron containing nickel may be subsequently treated in the open hearth or in the electricfurnace in the well known manner.
- This may be effected by employing a limited amount of the reducing agent sufficient only to reduce the oxides of metals, or such portions of them, as it may be desired to reduce, provided said metals are those in the lower order of sequence with respect to their relative disposition to reduction, that is to sa in the example I have given, the order 0 sequence would be: nickel, iron,
- My present object however is to confine the primary reduction and metallizing of the ore to the recovery of nickel and iron, in suitable proportions to form a nickel iron alloy'substantially freefromchromium and to effect the reduction of the chromium in a second operation.
- the reduced portion may be utilized in a refining furnace for the manufacture of a nickel steel, while the unreduced portion may be submitted to a secondary process of reduction for the recovery of the balance of the iron with the major part of the chromium, so as to form a chromium iron alloy.
- the heating of the metallized particles to their fusion point may be carried out, either in the same furnace as that which has been used for reduction, or in a separate furnace as a subsequent operation.
- the process is likewise susceptible of further modification, so as to complete, in said subsequent melting operation, the partial reduction previously eifectedin the reduction furnace.
- said melting operation may be associated with such refining steps as may be required for the production of a finished steel product.
- the slag remaining may then be submitted to a further process of reduction, in orderto metallize the unreduced chromium and/or other desired metallic components present therein.
- the slag portion may be further treated for the recovery therefrom of chromium, and/or other desired metals, by the action of a reducing agent, such as carbon, in amount suflicient to reduce these metallic components of the slag, said reduction being effected in a manner similar to that already described for the reduc-.
- a reducing agent such as carbon
- a carbonaceous reducing agent in amount substantially that required to reduce the nickel and a major portion of the iron' present in the ore so as to effect. their reduction, in raising the temperature of the mass, after saidjreduction has been efiected, to a. temperature preferably ranging from 2400 F. to 2500 F. so as to agglomerate the reduced metal, in cooling and in crushing the mass, in separating the agglomerate from the slag and in submitting said slag to further reduction in the presence of suflicient carbonaceous reducing agent to reduce the chromium and other reducible metallic compounds present in the slag.
- Patent o. 1;.7-17,160
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- Chemical & Material Sciences (AREA)
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- Geochemistry & Mineralogy (AREA)
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- General Life Sciences & Earth Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Materials Engineering (AREA)
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- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
nace charge. An
Patented 11-, me. 1 UNITED'STATES 1.111.1 PATENT OFFICE.
rum: 0. xrcnmim, or LEBANON, PENNSYLVANIA, ASSIGNOR r nnrnnennm srnar. COMPANY.
REDUCTION OF COMPLEX ,OBES.
Io Application filed December 4, 1924, Serial No. 753,810. Renewed larch 3, 1 927.
This invention relates to a process for the reduction of complexores whereby the metallic components of the ore can be recovered and substantially separated. It relates more 5 particularly to an iron ore having, associated therewith reducible com ounds of other metals asfor example, oxi es, some of which other metals it may be desired to alloy with a of further metallic components of the ore, re-
. maining unreduced after a first reduction process, for the purpose of producing a metallic productsuitable for furnace treatment,
which is an alloy of said unreduced components of the ore.
A particular ore which is amenable to treatment by. my process is the Mayari' iron ore of Cuba, said ore being mainly a limonite associllligd with chromite, and containing apao proxi tely 2.00% chromium, .7 5% nickel and 0.6% manganese. 1 This ore also contains a high percentage of moisture, which on removal leaves a product, mainly in a state of fine subdivision, unsuitable for a blast furglomerating process .is
therefore necessary ir the urpose of reducing the moisture content and at the same time rendering-the ore in a suitable condition'to be charged to the blast furnace. The blast fur- 40 nace product is a chromiferous pig iron, containi approximately 2% of chromium and 1% o nic e]. The chromium ma be sucvcessfu'll removed from this chromi erous pig iron by inerizing processes known to the art and the. dechromized iron containing nickel may be subsequently treated in the open hearth or in the electricfurnace in the well known manner.
Itv is, however, a purpose of this invention to produce a metallic iron product direct from the ore, having associated with'it substantially all of the nickel originally contained in the ore, but ractically free'of chromium, and -which will be-suitable for charging directly .556 into refining metallurgical furnaces, as for that the extent of the reduction may be conexample, an electric furnace. In this manner I intend'to eliminate the operations of agglomerating, of blast furnace reduction, and of Bessemerizing, hitherto practiced in the manufacture of steel from this ore. The retention of the nickel with the primary metallic product obtained by my process is obviously advantageous for the manufacture of nickel steels.
In this method of reduction I take advantage of the relative disposition to reduction of the various metallic components of the ore. It is well known that nickel is reduced more readily than iron, and that iron is reduced more readily than chromium at appro riate 70 temperatures, in the presence of a re ucing agent, asfor example, carbon, carbonaceous gases, or hydrogen. In other words, a reducing agent such as carbon, will take its oxygen from a nickel oxide in preference to taking it from a chromium oxide. By applying this principle of preferential reduction by means of reducing agents, such as carbon, carbonaceous gases or hydrogen, I have found trolled, as desired, within substantially narrow limits. This may be effected by employing a limited amount of the reducing agent sufficient only to reduce the oxides of metals, or such portions of them, as it may be desired to reduce, provided said metals are those in the lower order of sequence with respect to their relative disposition to reduction, that is to sa in the example I have given, the order 0 sequence would be: nickel, iron,
chromium.
I have found that an addition of coal amounting to 15% of the ore charge, said addition having been intimately mixed with the ore, and submitted to a temperature of approximately 1800 F., results in the reduction of substantially all the nickel and about 70% of the iron, without however effecting a reduction of the manganese and silicon, and only very slightly reducing the chromium.
With an additlon of 25% coal, and suitable temperatures as above described, a greater amount of the iron is reduced and a considerable portion'of the chromium is also re-' duced, the latter to the extent of approximately 30% of that present in the ore. With increasing quantities of coal the reduced metallic portion will carry further additional amounts of chromium.
' In carrying out my invention I mix fine coal or other carbonaceous material with the finely-divided ore, the coal in one instance being 15% of the weight of the ore. This mixture is charged to a suitable furnace, as for example, a rotary kiln furnace, and submitted therein to the direct heat of combustion gases. At a temperature of 1800 F., I have found that.
.mium, as shown in the appended table.
Coal Per 7 Per Per added Ni cent Fe cent Cr cent percent conreconre conreol-ore tent covtent covtent cov charged ery ery ery Original ore .88 53.90 2. 34 Reduction product- 15% 2.31 99.9 96.99 68.4 .24 3.75 Reduction product. 20% 2.03 99.9 96.73 75.2 .65 11.23 Reduction product. 25% 1. 95 99. 8 95. 36 80. 2 1. 61 30. 02
My present object however is to confine the primary reduction and metallizing of the ore to the recovery of nickel and iron, in suitable proportions to form a nickel iron alloy'substantially freefromchromium and to effect the reduction of the chromium in a second operation.
In order to subsequently reduce the chromium, it is necessary to separate the products of the primary reduction, so that the reduced portion may be utilized in a refining furnace for the manufacture of a nickel steel, while the unreduced portion may be submitted to a secondary process of reduction for the recovery of the balance of the iron with the major part of the chromium, so as to form a chromium iron alloy.
It will be obvious to those skilled in the art, that the combined products of my primary reduction process may be heated to a temperature corresponding to the fusion points of the reduced metals, which in the example I have given will be principall nickel and iron. At these temperatures t e metallized particles may be caused to flow from the slag, in a. manner well known in metallurgical practice.
It will also be obvious that the heating of the metallized particles to their fusion point may be carried out, either in the same furnace as that which has been used for reduction, or in a separate furnace as a subsequent operation. The process is likewise susceptible of further modification, so as to complete, in said subsequent melting operation, the partial reduction previously eifectedin the reduction furnace. Furthermore, said melting operation may be associated with such refining steps as may be required for the production of a finished steel product. The slag remaining may then be submitted to a further process of reduction, in orderto metallize the unreduced chromium and/or other desired metallic components present therein.
The separation of the metalized particles inayhowever be effected in asomewhatdifferent manner. I have discovered that by raising the temperature of the product, resulting from the primary reduction, to a point between 2300 and 2400 F., the reduced or metallized portions dispersed in the mass are caused to agglomerate, .while the slag forming portion remains unchanged. On cooling and crushing the mass, this metallic agglomeration is readily separable from the slag by magnetic, by electro-static or by mechanical means, and is then in a condition eminently suitable for a refining operation in a metallurgical furnace. The slag portion may be further treated for the recovery therefrom of chromium, and/or other desired metals, by the action of a reducing agent, such as carbon, in amount suflicient to reduce these metallic components of the slag, said reduction being effected in a manner similar to that already described for the reduc-.
tion of the nickel and of the major portion of the iron. This secondary reduction results in a metallized product comprising metallic chromium, the balance of the iron left unreduced in the first reduction process, and small amounts of manganese and silicon; the remaining constituents of the ore forming the secondary reduction slag.
While I have taken as an example of my process a nickel bearing chromiferous iron ore, it is evident that the process is equally applicable to any complex ore containing reducible metallic compounds, and that a similar selective reduction of any of said compounds may be eifected in the manner aforementioned, provided the desired selection is in the natural sequence of their individual dispositions to reduction. It is also evident that one of the means employed in the second step of'my process, devised to effect the agglomeration of metallic particles widely diffused in a complex mass, (said agglomera- I tion being a preliminary step to their separation from the slag by magnetic, electro-static or other mechanical means), is susceptible of wide application. Hence it will be obvious to those skilled in the art that my invention is susceptible of various'changes and modifications without departing from the spirit thereof, and I desire, therefore, that only such limitations shall be placed thereupon as are imposed by the prior art, or as are specifically set forth in the appended claims.
In certain of the claims which follow, I refer to my process being applicable to the separation of components not widely different in their reduction temperatures. By this I intend to convey the idea that the process is applicable to complex ores or other associaembo iment of the invention which has been Q I claim as new and desire to secure by Letters Patent is:
1. The process ofselectively reducing the reducible components of a com lex ore which components are not widely di erent in their reduction temperatures, which consists in,
heating the ore to a suitable temperature with sufficient reducing agents to substantially reduce such of the more readily reducible components it may be desired to separate primarily from the ore, said,reducing temperature bein lower than the fusion point of the desire component, in heating the mass after said reduction has been effected to a higher temperature at which a substantial agglomeration of the dispersed metallic articles may be efiected, in cooling and in crus ing the mass, in effecting the mechanical separation of the metallic agglomerate from the unreduced portion of the mass, and-in submitting said unreduced portion to a secondary reduction by heating it at a suitable temperature I with suflicient reducing agent to reduce such further components as may be desired.
2. The process ofselectively reducing a nickel bearing chromi'ferous iron ore, which consists in heating the ore to'a temperature preferably ranging from 1750 to 1900 F. in
the presence of a carbonaceous reducing agent in amount substantially that required to reduce the nickel and a major portion of the iron' present in the ore so as to effect. their reduction, in raising the temperature of the mass, after saidjreduction has been efiected, to a. temperature preferably ranging from 2400 F. to 2500 F. so as to agglomerate the reduced metal, in cooling and in crushing the mass, in separating the agglomerate from the slag and in submitting said slag to further reduction in the presence of suflicient carbonaceous reducing agent to reduce the chromium and other reducible metallic compounds present in the slag.
3. The process of selectively reducing .a nickel bearing ehromiferousiron ore, which consists in intimately mixing with the ore further heating the roasted mass to a tem-' perature preferably between 2400 F. and
2500 F. so as to agglomerate the metallic particles dispersed therein, in cooling and crushing the mass, in separating the crushed metallic agglomerate from the unreduced portion of the mass by magnetic separation, and in submitting said unreduced portion to a further reduction by roasting it at a suitable temperature in the presence of substantially sufficient carbonaceous reducing a ent to reduce the oxide of chromium and ot er reducible compounds present in said unreduced portion.
4-. The process of selectively reducing a nickel bearing chromiferou's iron ore, which consists in intimately mixing with'the ore substantially suflicientcarbonaceous reducing agent to reduce the oxides of nickel and part of the oxides of iron present in the ore, in roasting the mixture in a suitable furnace at a temperature preferably between 17 50 F. and 1900 F. so as to effect the reduction of the nickel and of the iron, in further heating the roasted mass to a temperature preferably between 2400-F. and 2500 F. so as to ag- 1 glomerate the metallic particles dispersed therein, in cooling and crushing the mass, in removing the crushed. metallic agglomerate from the unreduced portion of the mass, by mechanical separation, and in submitting said unreduced portion to a further reduction by roasting it at a suitable temperature in the presence of substantially suflicient carbonaceous reducing agent to reduce the oxide of chromium and other reducible compounds present insaid unreduced rtion.
5. The process of. selectively reducing a nickel bearing chromiferous iron ore, which consists in intimately mixing with the ore substantially sufiicient reducin agent to reduce the oxides of nickel an part of the oxides of iron present in theore, n roasting the mixture in a suitable furnace at a tempera.-
ture preferably .between 17 50 F. and 1900 F. so as to effect the reduction of the nickel and of' the iron, in further heatin the roasted mass to a'temperature preferab y, be-
10 under the influence of sufiicient reducing agent and at temperatures suitable for reducing principally a desired component, said temperatures being in each case lower than the fusion point of the desired reduction product, and raising the temperature atthe end of each reduction to a degree favorable to agglomeration of the reduced components,
but insuificient to fuse the mass, and separating the agglomerate from the remainder o the mass.
In testimony whereof I hereunto afiix my signature this twenty first day of November,
FRANK O. KICHLINE.
GERTIFIGATEOF CORRECTION.
Patent o. 1;.7-17,160.
Granted June 11, 1929, o
FRANK O. KICHLINE.
- It is hereby-certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 1, line 9, for the word 'Zis" read "maybe"; and that the said Letters Patent should be read'with this correction therein that the same may conform to the record of the case in the Patent Office;
I Si'zned and sealed this lthday of Ahgust, A. 1). 1929.
i (se -1 M. J. Moore, Acting Commissioner of Patents.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US753810A US1717160A (en) | 1924-12-04 | 1924-12-04 | Reduction of complex ores |
Applications Claiming Priority (1)
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US753810A US1717160A (en) | 1924-12-04 | 1924-12-04 | Reduction of complex ores |
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US1717160A true US1717160A (en) | 1929-06-11 |
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US753810A Expired - Lifetime US1717160A (en) | 1924-12-04 | 1924-12-04 | Reduction of complex ores |
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Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2448882A (en) * | 1943-12-13 | 1948-09-07 | Electro Chimie Metal | Method for deironing chromium ore |
US2450343A (en) * | 1947-02-01 | 1948-09-28 | E J Lavino & Co | Treating oxide ores |
US2526659A (en) * | 1945-03-09 | 1950-10-24 | Eugene S Harman | Continuous smelting process |
US2582469A (en) * | 1948-08-11 | 1952-01-15 | Marvin J Udy | Metallurgy |
US2674531A (en) * | 1948-05-18 | 1954-04-06 | Marvin J Udy | Iron recovery |
US2704248A (en) * | 1949-11-07 | 1955-03-15 | Madaras Corp | Method of separating ferrous metal from its gangue |
US2811434A (en) * | 1954-12-21 | 1957-10-29 | Nat Lead Co | Process for treating ilmenite-containing materials to produce metallic iron concentrates and titanium dioxide concentrates |
US2879158A (en) * | 1954-04-08 | 1959-03-24 | Duisburger Kupferhuette | Method for the separation of impurities from cobalt-containing materials |
US2939782A (en) * | 1957-09-26 | 1960-06-07 | Julius D Madaras | Metallurgical refining process |
US2969281A (en) * | 1958-01-17 | 1961-01-24 | American Metal Climax Inc | Process for making spherical metal particles |
US2995455A (en) * | 1958-06-25 | 1961-08-08 | Tohoku Denki Seitetsu Kabushik | Method of recovering nickel and iron from laterite ores by preferential reduction |
US3077396A (en) * | 1958-08-09 | 1963-02-12 | Lucas S Mcussoulos | Method of feni alloy production from nickel bearing iron ores |
US3083090A (en) * | 1958-09-22 | 1963-03-26 | United Steel Companies Ltd | Production of sinter |
US3100700A (en) * | 1960-04-25 | 1963-08-13 | Freeport Sulphur Co | Recovery of nickel and cobalt by reduction and leaching |
US3131053A (en) * | 1961-05-22 | 1964-04-28 | Dow Chemical Co | Production of metallic iron and silicate glass |
US3165398A (en) * | 1962-08-31 | 1965-01-12 | Yawata Iron & Steel Co | Method of melting sponge iron |
US3238039A (en) * | 1964-07-22 | 1966-03-01 | Yawata Iron & Steel Co | Process for separating non-molten slag from nickel chromium-containing iron ores |
US3272616A (en) * | 1963-12-30 | 1966-09-13 | Int Nickel Co | Method for recovering nickel from oxide ores |
US3388870A (en) * | 1965-04-07 | 1968-06-18 | Int Nickel Co | Upgrading of lateritic ores |
US3453101A (en) * | 1963-10-21 | 1969-07-01 | Fuji Iron & Steel Co Ltd | Process for treating nickeliferous ore |
US3503735A (en) * | 1966-05-19 | 1970-03-31 | Hanna Mining Co | Process of recovering metallic nickel from nickeliferous lateritic ores |
US3656935A (en) * | 1970-04-24 | 1972-04-18 | Univ Minnesota | Process for recovering nickel from nickel ores |
-
1924
- 1924-12-04 US US753810A patent/US1717160A/en not_active Expired - Lifetime
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2448882A (en) * | 1943-12-13 | 1948-09-07 | Electro Chimie Metal | Method for deironing chromium ore |
US2526659A (en) * | 1945-03-09 | 1950-10-24 | Eugene S Harman | Continuous smelting process |
US2450343A (en) * | 1947-02-01 | 1948-09-28 | E J Lavino & Co | Treating oxide ores |
US2674531A (en) * | 1948-05-18 | 1954-04-06 | Marvin J Udy | Iron recovery |
US2582469A (en) * | 1948-08-11 | 1952-01-15 | Marvin J Udy | Metallurgy |
US2704248A (en) * | 1949-11-07 | 1955-03-15 | Madaras Corp | Method of separating ferrous metal from its gangue |
US2879158A (en) * | 1954-04-08 | 1959-03-24 | Duisburger Kupferhuette | Method for the separation of impurities from cobalt-containing materials |
US2811434A (en) * | 1954-12-21 | 1957-10-29 | Nat Lead Co | Process for treating ilmenite-containing materials to produce metallic iron concentrates and titanium dioxide concentrates |
US2939782A (en) * | 1957-09-26 | 1960-06-07 | Julius D Madaras | Metallurgical refining process |
US2969281A (en) * | 1958-01-17 | 1961-01-24 | American Metal Climax Inc | Process for making spherical metal particles |
US2995455A (en) * | 1958-06-25 | 1961-08-08 | Tohoku Denki Seitetsu Kabushik | Method of recovering nickel and iron from laterite ores by preferential reduction |
US3077396A (en) * | 1958-08-09 | 1963-02-12 | Lucas S Mcussoulos | Method of feni alloy production from nickel bearing iron ores |
US3083090A (en) * | 1958-09-22 | 1963-03-26 | United Steel Companies Ltd | Production of sinter |
US3100700A (en) * | 1960-04-25 | 1963-08-13 | Freeport Sulphur Co | Recovery of nickel and cobalt by reduction and leaching |
US3131053A (en) * | 1961-05-22 | 1964-04-28 | Dow Chemical Co | Production of metallic iron and silicate glass |
US3165398A (en) * | 1962-08-31 | 1965-01-12 | Yawata Iron & Steel Co | Method of melting sponge iron |
US3453101A (en) * | 1963-10-21 | 1969-07-01 | Fuji Iron & Steel Co Ltd | Process for treating nickeliferous ore |
US3272616A (en) * | 1963-12-30 | 1966-09-13 | Int Nickel Co | Method for recovering nickel from oxide ores |
US3238039A (en) * | 1964-07-22 | 1966-03-01 | Yawata Iron & Steel Co | Process for separating non-molten slag from nickel chromium-containing iron ores |
US3388870A (en) * | 1965-04-07 | 1968-06-18 | Int Nickel Co | Upgrading of lateritic ores |
US3503735A (en) * | 1966-05-19 | 1970-03-31 | Hanna Mining Co | Process of recovering metallic nickel from nickeliferous lateritic ores |
US3656935A (en) * | 1970-04-24 | 1972-04-18 | Univ Minnesota | Process for recovering nickel from nickel ores |
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