US2096779A - Process for reducing oxidized ores of zinc - Google Patents
Process for reducing oxidized ores of zinc Download PDFInfo
- Publication number
- US2096779A US2096779A US713982A US71398234A US2096779A US 2096779 A US2096779 A US 2096779A US 713982 A US713982 A US 713982A US 71398234 A US71398234 A US 71398234A US 2096779 A US2096779 A US 2096779A
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- US
- United States
- Prior art keywords
- zinc
- reducing
- retort
- coke
- carbon monoxide
- Prior art date
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- Expired - Lifetime
Links
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title description 32
- 229910052725 zinc Inorganic materials 0.000 title description 32
- 239000011701 zinc Substances 0.000 title description 32
- 238000000034 method Methods 0.000 title description 14
- 239000000571 coke Substances 0.000 description 19
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 15
- 229910002091 carbon monoxide Inorganic materials 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 11
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 239000003638 chemical reducing agent Substances 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 239000011872 intimate mixture Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000003500 flue dust Substances 0.000 description 1
- -1 for example Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 238000006467 substitution reaction Methods 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
- C22B19/00—Obtaining zinc or zinc oxide
- C22B19/04—Obtaining zinc by distilling
- C22B19/14—Obtaining zinc by distilling in vertical retorts
Definitions
- This invention relates to the reduction of oxidized ores ofzinc.
- zinc oxide in a finely-divided state is introduced into a suitable reducing atmosphere under such conditions that the zinc is almost instantaneously reduced to zinc vapor which, after passage through a suitable reducing and filtering medium, is readily condensed to metallic zinc;
- Fig. 2 is a cross-section taken along the line 2-2 of Fi 1.
- FIG. 1 it! represents a combustion chamber defined by wall ll, fioor l2 and roof l3. Positioned in combustion chamber in are vertical retort M and coke filter l5 which .terminate at their lower ends into seals l6 and i1 respectively. Insulated storage bin it having feeding device I9 is connected to inlet 20 of retort it via pipe 2i while bin 22 associated with gates 23 is positioned above filter I 5. Passageways between retort M and filter l5 are provided by means of bafiies 24 in the common wall 25.
- a pipe 26 leads from the top of filter ii to condenser 21 equipped with tapping spout 28.
- Pipe 29 leads from the top of condenser 21 to storage container '30.
- with valve 32 is inserted in pipe 29 between condenser 21 and storage container 30.
- Pipe 33 leads from.
- the invention may be practised as follows: Theretort It and coke filter iii are brought to the proper temperature, preferably above 1100 C., by heat supplied by burners 40 inserted in the refractory wall M of combustion chamber Ill.
- the preheated charge comprising an intimate mixture of oxidized zinciferous material and coke dust in a finely divided state, preferably minus 200 55 mesh, is fed from bin it into pipe 2
- the charge passes downwardly through pipe 2
- the zinc vapor, carbon monoxide and any carbon dioxide then pass from retort l4 into coke filter l5 through the opening formed by bafiles 24 in common wall 25.
- any carbon dioxide is converted to carbon monoxide so that only zinc vapor and carbon monoxide enter the condenser 21.
- the coke filter also serves to separateout any dust carried over from the retort.
- the level of coke in the filter is' maintained by introducing the coke as needed from hopper 22 via gates 23 and residues from the retort and coke filter are periodically removed through seals 5 and I1 respectively.
- the zinc vapor is condensed to metal and may be removed through spout 28 while the carbon monoxide passes to storage container 30- from whence it is withdrawn as needed and supplied by blower 34 to inlets 20 and 36.
- Any carbon monoxide in excessof that needed for use as the reducing'agent in the retort may be withdrawn from the system through pipes 3
- the process of the invention marks a distinct advance in the art of reducing oxidized ores of zinc.
- the reducing reaction is accelerated to such a degree that it takes place practically instantaneously which is a remarkable improvement over the prior art retort processes which required hours for the complete reduction of a comparatively small charge.
- carbon monoxide has been specified as the reducing gas bu inasmuch finely-divided state in gaseous suspension, it will be readily appreciated that other reducing agents may be employed within the scopeof the invention.
- methane CH4 is probably, the most important. In fact, it is superior to carbon monoxide in some respects, for example, the reduction proceeds at a more rapid rate and is effected at lower temperatures. Also, with methane, the addition of carbon to the charge may be eliminated.
- the invention is applicable to the treatment of oxides of other metals, for example, cadmium, which require for reduction, a temperature greater than the boiling point of the metal.
- the method which comprises injecting an atomized charge of such ore and coke dust into a'preheated retort filled with carbon monoxide, passing the products of reaction through anincandescent layer of coke and into a .condenser in which zinc vapor is condensed to liquid zinc, withdrawing carbon monoxide from said condenser and recycling same to the retort for treating fur ther quantities of such atomized charge.
- a process for reducing oxidized ores of zinc which comprises forming an intimately mixedcharge of comminuted zinc ore and solid carbonaceous reducing agent, preheating said charge and passing same through a preheated retort maintained atzinc reduction temperatures thereby efiecting practically instantaneous and substantially complete reduction of theore, withdrawing the resulting zinc vapor and gaseous products of reaction from the retort through a. bed of incandescent coke and recovering zinc therefrom by condensation.
- the process for reducing oxidized ores of zinc which comprises continuously charging such ore and carbonaceous reducing agent to a retort maintained at zinc reduction temperatures, said ore and said reducing agent being charged to the 8.
- the process for treating zinc in the oxidized state to produce metallic zinc which comprises continuously passing oxidized zinciferous material in a finely-divided state through a hot reducing atmosphere to reduce said zinciferous material in gaseous suspension, passing the resulting zinc vapors and gaseous products of reaction through an incandescent, carbonaceous bed, and
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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
Get. 26,1937. 6: P. BARTHOLOMEW ET-AL 2,096,779
I PROCESS FOR REDUCING OXIDIZED GEES OF ZINC I Filed March '5, i934 Patented Oct. 26, 1 937 UNITED STATES PROCESS FOR REDUCING OXIDIZED QRES OF ZINC George P. Bartholomew, Essex Fells, N. J., and
Edward P. Fleming, Salt Lake City, Utah, assignors to American smelting and Refining' Company, New York, N. Y., a corporation of New Jersey Application March 5, 1934, Serial No. 713,982
8 Claims.
This invention relates to the reduction of oxidized ores ofzinc.
' In accordance with the invention, zinc oxide in a finely-divided state is introduced into a suitable reducing atmosphere under such conditions that the zinc is almost instantaneously reduced to zinc vapor which, after passage through a suitable reducing and filtering medium, is readily condensed to metallic zinc;
Although the novel features which are believed to be, characteristic of the invention are particularly pointed out in the appended claims, the invention itself, as to its objects and advantages, and the manner in which it may be carried out, will be better understood by referring to the following description taken in connection with the accompanying drawing forming a part thereof, in which Fig. 1 'is a view of an apparatus-suitable for practising the process of the invention; and
Fig. 2 is a cross-section taken along the line 2-2 of Fi 1.
Referring to the drawing, it! represents a combustion chamber defined by wall ll, fioor l2 and roof l3. Positioned in combustion chamber in are vertical retort M and coke filter l5 which .terminate at their lower ends into seals l6 and i1 respectively. Insulated storage bin it having feeding device I9 is connected to inlet 20 of retort it via pipe 2i while bin 22 associated with gates 23 is positioned above filter I 5. Passageways between retort M and filter l5 are provided by means of bafiies 24 in the common wall 25.
A pipe 26 leads from the top of filter ii to condenser 21 equipped with tapping spout 28. Pipe 29 leads from the top of condenser 21 to storage container '30. An ofitake pipe 8| with valve 32 is inserted in pipe 29 between condenser 21 and storage container 30. Pipe 33 leads from.
. Employing the above apparatus, the invention may be practised as follows: Theretort It and coke filter iii are brought to the proper temperature, preferably above 1100 C., by heat supplied by burners 40 inserted in the refractory wall M of combustion chamber Ill. The preheated charge comprising an intimate mixture of oxidized zinciferous material and coke dust in a finely divided state, preferably minus 200 55 mesh, is fed from bin it into pipe 2| by feeding device l9. The charge passes downwardly through pipe 2|, ls atomized and injected into preheated retort I! through inlet 20 with carbon 4 monoxide gas which has been preheated by passing through the coil in the flue 38 as shown in the drawing. Upon entering the retort which contains carbon monoxide gas introduced through pipe 35, the zinc is almost instantly reduced in gaseous suspension according to the reaction ZnO+CO ZN+COa while the carbon present reacts with the carbon dtoxide to form carbon monoxide according to the reaction COz+C- 2CO.
The zinc vapor, carbon monoxide and any carbon dioxide then pass from retort l4 into coke filter l5 through the opening formed by bafiles 24 in common wall 25. By passing the zinc vapor and gases through the incandescent coke column, any carbon dioxide is converted to carbon monoxide so that only zinc vapor and carbon monoxide enter the condenser 21. -The coke filter also serves to separateout any dust carried over from the retort. The level of coke in the filter is' maintained by introducing the coke as needed from hopper 22 via gates 23 and residues from the retort and coke filter are periodically removed through seals 5 and I1 respectively.
in condenser 21 the zinc vapor is condensed to metal and may be removed through spout 28 while the carbon monoxide passes to storage container 30- from whence it is withdrawn as needed and supplied by blower 34 to inlets 20 and 36. Any carbon monoxide in excessof that needed for use as the reducing'agent in the retort may be withdrawn from the system through pipes 3| by opening valve 32 and used as fuel for heating the combustion chamber Iii by means of suitable connections (not shown) with fuel supply line 39.
The process of the invention marks a distinct advance in the art of reducing oxidized ores of zinc. By atomizing the ore, thus obtaining a maximum surface for reaction with the reducing gas, and injecting the minute particles into the preheated reducing atmosphere, the reducing reaction is accelerated to such a degree that it takes place practically instantaneously which is a remarkable improvement over the prior art retort processes which required hours for the complete reduction of a comparatively small charge. W
In the example given, carbon monoxide has been specified as the reducing gas bu inasmuch finely-divided state in gaseous suspension, it will be readily appreciated that other reducing agents may be employed within the scopeof the invention. Of these, methane (CH4) is probably, the most important. In fact, it is superior to carbon monoxide in some respects, for example, the reduction proceeds at a more rapid rate and is effected at lower temperatures. Also, with methane, the addition of carbon to the charge may be eliminated.
In addition to treating oxidized ores of zinc, the invention is applicable to the treatment of oxides of other metals, for example, cadmium, which require for reduction, a temperature greater than the boiling point of the metal.
While certain novel feaures of the invention have been disclosed and are pointed out in the annexed claims, it -will be understood that various omissions, substitutions and changes may be made by those skilled in the art without departing from the spirit of the invention.
What is claimed is:
1. The process of treating zinciierous ore which comprises injecting an intimate mixture of such ore and coke in a finely-divided state into a hot carbon monoxide atmosphere thereby reducing the zinc to vapor, passing the products of reaction through a bed of incandescent coke thereby filtering out flue dust and reducing any carbon dioxide to carbon monoxide and condensing the zinc from the gases emerging from the coke filter. f
2. In reducing zinc, the process which comprises injecting an intimate mixture of zinc oxide and coke in a finestate of subdivision into a preheated atmosphere of carbon monoxide, passing the products of reaction through a bed of incandescent coke and condensing the zinc vapor emerging from the .bed of coke.
3. In reducing oxidized ores of zinc, the method which comprises injecting an atomized charge of such ore and coke dust into a'preheated retort filled with carbon monoxide, passing the products of reaction through anincandescent layer of coke and into a .condenser in which zinc vapor is condensed to liquid zinc, withdrawing carbon monoxide from said condenser and recycling same to the retort for treating fur ther quantities of such atomized charge.
4. The process for recovering zinc from oxidized ores thereof which consists in preheating a comminuted charge comprisingsaid ore and a solid reducing agent, feeding said charge into a preheated retort out of contact-with air in a manner calculated to reduce the ore in suspension, passing the products of reaction through a coke filter maintained under conditions favoring the reaction CO2+C 2CO and suitably condensing the zinc vapor emerging from said filter.
5. A process for reducing oxidized ores of zinc which comprises forming an intimately mixedcharge of comminuted zinc ore and solid carbonaceous reducing agent, preheating said charge and passing same through a preheated retort maintained atzinc reduction temperatures thereby efiecting practically instantaneous and substantially complete reduction of theore, withdrawing the resulting zinc vapor and gaseous products of reaction from the retort through a. bed of incandescent coke and recovering zinc therefrom by condensation.
6. The process for treating oxidized-ores of metals having reduction temperatures in excess of the boiling points of the respective metalswhich comprises forming a comminuted charge'of such an ore and a solid carbonaceous reducing agent, preheating said charge, passing said preheated charge through a retort maintained at reduction temperatures thereby reducing the ore in suspension, conducting the resulting gases and metal vapor from said retort to a condenser through an incandescent bed of carbonaceous reducing agent and condensing the metal vapor.
'7. The process for reducing oxidized ores of zinc which comprises continuously charging such ore and carbonaceous reducing agent to a retort maintained at zinc reduction temperatures, said ore and said reducing agent being charged to the 8. The process for treating zinc in the oxidized state to produce metallic zinc which comprises continuously passing oxidized zinciferous material in a finely-divided state through a hot reducing atmosphere to reduce said zinciferous material in gaseous suspension, passing the resulting zinc vapors and gaseous products of reaction through an incandescent, carbonaceous bed, and
suitably condensing zinc from the vapor emerging from said bed.
GEORGE P, BARTHOLOMEW. EDWARD P. FLEMING.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US713982A US2096779A (en) | 1934-03-05 | 1934-03-05 | Process for reducing oxidized ores of zinc |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US713982A US2096779A (en) | 1934-03-05 | 1934-03-05 | Process for reducing oxidized ores of zinc |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2096779A true US2096779A (en) | 1937-10-26 |
Family
ID=24868339
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US713982A Expired - Lifetime US2096779A (en) | 1934-03-05 | 1934-03-05 | Process for reducing oxidized ores of zinc |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2096779A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2457552A (en) * | 1946-01-17 | 1948-12-28 | New Jersey Zinc Co | Vertical retort process for zinc smelting |
| US2493823A (en) * | 1947-04-02 | 1950-01-10 | Nat Zinc Company Inc | Process for zinc smelting |
| US2497096A (en) * | 1945-04-20 | 1950-02-14 | Vernon F Parry | Process for the production of vaporizable metals |
| US2598742A (en) * | 1949-09-02 | 1952-06-03 | New Jersey Zinc Co | Smelting of zinciferous ore |
| US2637649A (en) * | 1949-09-02 | 1953-05-05 | New Jersey Zinc Co | Condensing zinc vapor |
| US3044870A (en) * | 1958-10-16 | 1962-07-17 | Callery Chemical Co | Production of sodium |
| US3414401A (en) * | 1965-03-11 | 1968-12-03 | Soc Metallurgique Imphy | Process for obtaining solid zinc from zinc vapour containing gases |
-
1934
- 1934-03-05 US US713982A patent/US2096779A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2497096A (en) * | 1945-04-20 | 1950-02-14 | Vernon F Parry | Process for the production of vaporizable metals |
| US2457552A (en) * | 1946-01-17 | 1948-12-28 | New Jersey Zinc Co | Vertical retort process for zinc smelting |
| US2493823A (en) * | 1947-04-02 | 1950-01-10 | Nat Zinc Company Inc | Process for zinc smelting |
| US2598742A (en) * | 1949-09-02 | 1952-06-03 | New Jersey Zinc Co | Smelting of zinciferous ore |
| US2637649A (en) * | 1949-09-02 | 1953-05-05 | New Jersey Zinc Co | Condensing zinc vapor |
| US3044870A (en) * | 1958-10-16 | 1962-07-17 | Callery Chemical Co | Production of sodium |
| US3414401A (en) * | 1965-03-11 | 1968-12-03 | Soc Metallurgique Imphy | Process for obtaining solid zinc from zinc vapour containing gases |
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