US2290843A - Method of recovering manganese - Google Patents
Method of recovering manganese Download PDFInfo
- Publication number
- US2290843A US2290843A US395236A US39523641A US2290843A US 2290843 A US2290843 A US 2290843A US 395236 A US395236 A US 395236A US 39523641 A US39523641 A US 39523641A US 2290843 A US2290843 A US 2290843A
- Authority
- US
- United States
- Prior art keywords
- manganese
- ores
- iron
- chlorides
- recovery
- 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
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- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title description 47
- 239000011572 manganese Substances 0.000 title description 47
- 229910052748 manganese Inorganic materials 0.000 title description 46
- 238000000034 method Methods 0.000 title description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 40
- 229910052742 iron Inorganic materials 0.000 description 19
- 150000001805 chlorine compounds Chemical class 0.000 description 13
- 239000007789 gas Substances 0.000 description 13
- 238000011084 recovery Methods 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 150000002739 metals Chemical class 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 4
- 229910000616 Ferromanganese Inorganic materials 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical class Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 3
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 3
- AMWRITDGCCNYAT-UHFFFAOYSA-L manganese oxide Inorganic materials [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910021380 Manganese Chloride Inorganic materials 0.000 description 2
- GLFNIEUTAYBVOC-UHFFFAOYSA-L Manganese chloride Chemical compound Cl[Mn]Cl GLFNIEUTAYBVOC-UHFFFAOYSA-L 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- 239000011565 manganese chloride Substances 0.000 description 2
- 229940099607 manganese chloride Drugs 0.000 description 2
- 235000002867 manganese chloride Nutrition 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- PPNAOCWZXJOHFK-UHFFFAOYSA-N manganese(2+);oxygen(2-) Chemical class [O-2].[Mn+2] PPNAOCWZXJOHFK-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910001021 Ferroalloy Inorganic materials 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000012716 precipitator Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- C22B47/00—Obtaining manganese
-
- 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
- Y02P10/20—Recycling
Definitions
- 'Ihis invention relates to a new and improved method of recovering manganese from manganiferous iron ores, and further to such a method adapted for use in connection with low grade iron ores with the subsequent separation of iron.
- the charge mixed with carbon is raised in temperature to a point Where the manganese is volatilized in the form of the oxide and carried out of the roasting furnace with the gases.
- the manganese is then recovered from the gas by using dust collectors of any type, and wet gas washers, or an electric precipitator, or any combination of such means of recovery.
- the recovered oxide is of a comparatively high purity and may subsequently be reduced in an electric furnace or may be sintered to form a high manganese content product for charging into the blast ⁇ furnace for the production of ferro-manganese.
- the volatilzation process may be carried out in any type of retort, coupled with a suitable condensing system for the recovery of the ⁇ oxide of manganese.
- the process of volatilization of manganese may also be carried out in a continuous manner on a traveling hearth,
- a grated hearth similar to that used in the sintering of ore, or any other hearth capable of withstanding high temperatures I prefer to mix the charge with carbon and place it on a moving grate or bed.
- the carbon in the charge is ignited by oil or other suitable means and the mass is raised to a high temperature which permits volatilization of the manganese and manganese oxides.
- the oxides of manganese and metallic manganese fumes are then recovered from the gas by means of a dust or fume recovery system.
- this invention the entire process is carried out at a comparatively low temperature and the metallics in the ore are taken away from the ore by volatilization rather than by melting and fluxing the gangue materials.
- a ilow sheet is shown giving a diagrammatic iiow of materials through the process.
- the lower part of the sheet shows diagrammatically the equipment required for reduction, volatilization and condensation and in the upper part of the sheet in diagrammatic form will be found the condensing system for handling the gases used in the process.
- the rst step in the process consists of charging the ore to a rotary kiln or multiple hearth type furnace in which the charge is dried and reduced with either solid carbon or other suitable means.
- hydrochloric acid is brought into contact with the charge and necessary heat is applied to volatilize the manganese and iron chlorides which are condensed in an adjoining chamber.
- These chlorides are conveyed to a kiln where they are contacted with hydrogen gas, and metallic manganese and iron are formed.
- the end products from the latter kiln that is, hydrochloric acid gas and other gases, are conveyed to an ordinary condensing tower where they are contacted with water and thence enter an ordinary condensing system.
- the products of combustion from the producer gas which is used in the last kiln are carried along with the hydrochloric gas and passed through the condensing system and any carbon or hydrogen remaining in the system from this combination are recirculated through the last kiln, as shown on the flow sheet.
- the process for the recovery of manganese from manganese bearing ores which comprises reducing the ores with carbon, treating the reduced ores with hydrochloric acid, heating and Volatilizing the manganese in the form of a chloride, condensing the manganese chloride, and treating the chloride with hydrogen to obtain metallic manganese.
- the process for the recovery of iron and manganese from ores bearing these metals which comprises reducing the ores with carbon, treating the reduced ores to form chlorides of iron and manganese, volatilizing and condensing the chlorides, treating them with hydrogen bearing gases to produce metallic iron and manganese, and separating the metals.
- the process for the recovery of iron and manganese from ores bearing these metals which comprises treating the ores to reduce iron and manganese oxides, treating the reduced metals to form chlorides of iron and manganese, volatilizing and condensing the chlorides, treating them with hydrogen bearing gases to produce metallic iron and manganese, and separating the metals.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
July 21, 1942. s. P. KINNEY 2,290,843
METHOD OF RECOVERING MANGANESE Filed May 26, 1941 MN INVENTOR Patented July 21, 1942 METHOD OF RECOVERING MANGANESE Selwyne P. Kinney, Pittsburgh, Pa., assignor to Minerals and Metals Corporation, New York, N. Y., a corporation of Delaware Application May 26, 1941, Serial No. 395,236
s claims.
'Ihis invention relates to a new and improved method of recovering manganese from manganiferous iron ores, and further to such a method adapted for use in connection with low grade iron ores with the subsequent separation of iron.
In the treatment of such ores I have found that in some cases it is more desirable to volatilize the manganese directly out of the ore, or to form a manganese product With a reagent, as, for example, chlorine, and volatilize the manganese chloride from the ore. In the process which is disclosed herein, I have found it is more desirable to take advantage ofthe phenomena of volatilization and to separate the manganese from the gangue in this manner rather than smelting where a fusion process is employed.
In the manufacture of ferro-manganese and other ferro alloys from manganese ores, a considerable loss is generally encountered due to volatilization of manganese. In the smelting of manganese ores for the production of ferromanganese in a blast furnace, the ore is mixed with limestone and coke for fuel. The shaft of this furnace is high and comparatively cool and even with a height of shaft of approximately 80 to 100', manganese is volatilized from the charge and the loss in the gases in the form of manganese or partially reduced oxide ranges from a minimum of 8% to sometimes as high as according to the operation.
I have noticed the tendency of the manganese to volatilize under the above described conditions, and in this invention I make use of volatilization for the recovery of the manganese from its ores and particularly its low grade ores containing large percentages of gangue and iron.
It is an object of the present invention to provide new and improved methods for the recovery of manganese from ores containing this material.
It is a further object to provide processes suitable for use with manganiferous iron ores and from low grade iron ores.
It is also an object to provide a method of this character in which the manganese is volatilized from the ores and is condensed from its volatile form and recovered as metallic manganese and manganese dioxide.
It is an additional object to provide a method by which the manganese may be recovered from the ores in the form of chlorides and the chlorides subsequently treated for the formation of the metallic manganese.
It is another object to provide methods of this character operation a hearth of carborundum or other suitable material can be used, which hearth is heated from the bottom and the charge is carried directly upon the hearth. The charge mixed with carbon is raised in temperature to a point Where the manganese is volatilized in the form of the oxide and carried out of the roasting furnace with the gases.
The manganese is then recovered from the gas by using dust collectors of any type, and wet gas washers, or an electric precipitator, or any combination of such means of recovery. The recovered oxide is of a comparatively high purity and may subsequently be reduced in an electric furnace or may be sintered to form a high manganese content product for charging into the blast` furnace for the production of ferro-manganese. In the process of recovery of manganese from 10W grade ores, the volatilzation process may be carried out in any type of retort, coupled with a suitable condensing system for the recovery of the `oxide of manganese. The process of volatilization of manganese may also be carried out in a continuous manner on a traveling hearth,
for instance, a grated hearth similar to that used in the sintering of ore, or any other hearth capable of withstanding high temperatures. In this case I prefer to mix the charge with carbon and place it on a moving grate or bed. The carbon in the charge is ignited by oil or other suitable means and the mass is raised to a high temperature which permits volatilization of the manganese and manganese oxides. The oxides of manganese and metallic manganese fumes are then recovered from the gas by means of a dust or fume recovery system.
In the recovery of manganese from low grade manganese ores or from low grade manganiferous ores, I have found it possible to eiect a separation of manganese and iron or a recovery of manganese alone by the formation of chlorides of these metals. It is a Well known fact that chlorides of manganese and iron are easily formed in which iron recovered with the manand that these chlorides volatilize at a comparatively low temperature. It is also known that the chlorides of these metals may be formed directly from the oxide, although in some cases it is preferable to form them directly from the individual metals.
In the process of the recovery of manganese I prefer to make a direct reduction either with gas `or solid carbon of the oxides oi' manganese and iron as a rst step. The reactions are as follows:
After reduction, the metals are contacted with hydrochloric acid gas with the resultant formation of manganese and iron chlorides as shown in the following equations covering this second step in the process:
In this second step, I prefer to apply heat t volatilize the manganese and iron chlorides out of gangue material. In the third step, these chlorides are condensed and treated with recirculated hydrogen or hydrogen bearing gas for the formation of metallic manganese and metallic iron and hydrochloric acid gas. The equations are as follows:
aration of the manganese from the iron, I prefer to use a magnetic or other suitable means. By
this invention the entire process is carried out at a comparatively low temperature and the metallics in the ore are taken away from the ore by volatilization rather than by melting and fluxing the gangue materials.
In the accompanying drawing, a ilow sheet is shown giving a diagrammatic iiow of materials through the process. The lower part of the sheet shows diagrammatically the equipment required for reduction, volatilization and condensation and in the upper part of the sheet in diagrammatic form will be found the condensing system for handling the gases used in the process.
The rst step in the process consists of charging the ore to a rotary kiln or multiple hearth type furnace in which the charge is dried and reduced with either solid carbon or other suitable means. In this reduction furnace hydrochloric acid is brought into contact with the charge and necessary heat is applied to volatilize the manganese and iron chlorides which are condensed in an adjoining chamber. These chlorides are conveyed to a kiln where they are contacted with hydrogen gas, and metallic manganese and iron are formed. The end products from the latter kiln, that is, hydrochloric acid gas and other gases, are conveyed to an ordinary condensing tower where they are contacted with water and thence enter an ordinary condensing system.
The products of combustion from the producer gas which is used in the last kiln are carried along with the hydrochloric gas and passed through the condensing system and any carbon or hydrogen remaining in the system from this combination are recirculated through the last kiln, as shown on the flow sheet.
While I have described in detail certain preferred methods of carrying out my invention, it is capable of modication to meet differing conditions and requirements, and I contemplate such variations as come within the spirit and scope of the appended claims.
What is claimed is:
1. The process for the recovery of manganese from manganese bearing ores, which comprises reducing the ores with carbon, treating the reduced ores with hydrochloric acid, heating and Volatilizing the manganese in the form of a chloride, condensing the manganese chloride, and treating the chloride with hydrogen to obtain metallic manganese.
2. The process for the recovery of iron and manganese from ores bearing these metals, which comprises reducing the ores with carbon, treating the reduced ores to form chlorides of iron and manganese, volatilizing and condensing the chlorides, treating them with hydrogen bearing gases to produce metallic iron and manganese, and separating the metals.
3. The process for the recovery of iron and manganese from ores bearing these metals, which comprises treating the ores to reduce iron and manganese oxides, treating the reduced metals to form chlorides of iron and manganese, volatilizing and condensing the chlorides, treating them with hydrogen bearing gases to produce metallic iron and manganese, and separating the metals.
SELWYNE P. KINNEY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US395236A US2290843A (en) | 1941-05-26 | 1941-05-26 | Method of recovering manganese |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US395236A US2290843A (en) | 1941-05-26 | 1941-05-26 | Method of recovering manganese |
Publications (1)
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US2290843A true US2290843A (en) | 1942-07-21 |
Family
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US395236A Expired - Lifetime US2290843A (en) | 1941-05-26 | 1941-05-26 | Method of recovering manganese |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2596073A (en) * | 1951-06-14 | 1952-05-06 | Henry L Crowley & Co Inc | Process of selectively reducing ferrous chloride in the solid phase from a solid mixture of fecl2 and mncl2 |
US2629650A (en) * | 1947-05-13 | 1953-02-24 | Internat Minerals & Chemicals | Method of purifying phosphate rock containing iron impurities |
US2658813A (en) * | 1951-10-05 | 1953-11-10 | Republic Steel Corp | Process of selectively chloridizing manganese in the treatment of materials containing iron and manganese |
US2701761A (en) * | 1951-05-05 | 1955-02-08 | Henry L Crowley & Company Inc | Integrated cyclic process for producing metallic iron from iron oxide-containing material |
US2701762A (en) * | 1951-09-13 | 1955-02-08 | Henry L Crowley & Company Inc | Integrated cyclic process for producing metallic iron from iron oxidecontaining material |
US2709131A (en) * | 1949-06-24 | 1955-05-24 | Armeo Steel Corp | Method of producing concentrates of iron and manganese from low-grade ores and slags |
US2723912A (en) * | 1949-07-21 | 1955-11-15 | United Steel Companies Ltd | Method of and plant for the treatment of iron ore |
US2752299A (en) * | 1952-01-08 | 1956-06-26 | Walter M Weil | Electrolytic production of manganese and ferromanganese |
DE1130185B (en) * | 1956-02-22 | 1962-05-24 | Walter M Weil | Process for the extraction of manganese from substances containing manganese |
US3244512A (en) * | 1963-03-04 | 1966-04-05 | Alberta Res Council | Hydrometallurgical iron process |
US3252787A (en) * | 1963-06-11 | 1966-05-24 | Oceanic Process Corp | Process for producing titanium dioxide concentrate and other useful products from ilmenite and similar ores |
US3258332A (en) * | 1962-10-16 | 1966-06-28 | Alberta Res Council | Hydrometallurgical method for selective metal removal |
US20220325375A1 (en) * | 2019-08-14 | 2022-10-13 | Minex Technology Group Limited | Metal recovery process |
-
1941
- 1941-05-26 US US395236A patent/US2290843A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2629650A (en) * | 1947-05-13 | 1953-02-24 | Internat Minerals & Chemicals | Method of purifying phosphate rock containing iron impurities |
US2709131A (en) * | 1949-06-24 | 1955-05-24 | Armeo Steel Corp | Method of producing concentrates of iron and manganese from low-grade ores and slags |
US2723912A (en) * | 1949-07-21 | 1955-11-15 | United Steel Companies Ltd | Method of and plant for the treatment of iron ore |
US2701761A (en) * | 1951-05-05 | 1955-02-08 | Henry L Crowley & Company Inc | Integrated cyclic process for producing metallic iron from iron oxide-containing material |
US2596073A (en) * | 1951-06-14 | 1952-05-06 | Henry L Crowley & Co Inc | Process of selectively reducing ferrous chloride in the solid phase from a solid mixture of fecl2 and mncl2 |
US2701762A (en) * | 1951-09-13 | 1955-02-08 | Henry L Crowley & Company Inc | Integrated cyclic process for producing metallic iron from iron oxidecontaining material |
US2658813A (en) * | 1951-10-05 | 1953-11-10 | Republic Steel Corp | Process of selectively chloridizing manganese in the treatment of materials containing iron and manganese |
US2752299A (en) * | 1952-01-08 | 1956-06-26 | Walter M Weil | Electrolytic production of manganese and ferromanganese |
DE1130185B (en) * | 1956-02-22 | 1962-05-24 | Walter M Weil | Process for the extraction of manganese from substances containing manganese |
US3258332A (en) * | 1962-10-16 | 1966-06-28 | Alberta Res Council | Hydrometallurgical method for selective metal removal |
US3244512A (en) * | 1963-03-04 | 1966-04-05 | Alberta Res Council | Hydrometallurgical iron process |
US3252787A (en) * | 1963-06-11 | 1966-05-24 | Oceanic Process Corp | Process for producing titanium dioxide concentrate and other useful products from ilmenite and similar ores |
US20220325375A1 (en) * | 2019-08-14 | 2022-10-13 | Minex Technology Group Limited | Metal recovery process |
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