US512531A - Process of treating ores - Google Patents
Process of treating ores Download PDFInfo
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- US512531A US512531A US512531DA US512531A US 512531 A US512531 A US 512531A US 512531D A US512531D A US 512531DA US 512531 A US512531 A US 512531A
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- United States
- Prior art keywords
- ore
- coal
- furnace
- ores
- blast
- Prior art date
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- 238000000034 method Methods 0.000 title description 13
- 230000008569 process Effects 0.000 title description 13
- 239000003245 coal Substances 0.000 description 19
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 10
- 239000005864 Sulphur Substances 0.000 description 10
- 239000000446 fuel Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 238000002485 combustion reaction Methods 0.000 description 8
- 238000003723 Smelting Methods 0.000 description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 7
- 229910052725 zinc Inorganic materials 0.000 description 7
- 239000011701 zinc Substances 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 239000003500 flue dust Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000002366 mineral element Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 241001062472 Stokellia anisodon Species 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 238000004939 coking Methods 0.000 description 3
- 239000011133 lead Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 230000001427 coherent effect Effects 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 150000003568 thioethers Chemical class 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
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
Definitions
- Natural granular ores may also be used or the ore may be crushed to pea and dust size, and then operated on.
- material especially that containing the sulphides of iron, copper, zinc and' lead if mixed with any slack or waste coal, and submitted to an air blast either on perforated grates or on closed hearths, may be quickly cemented or clinkered and that such material, or clinker, can be made to retain a large portion of the fuel in an available form and that in this spongy or cemented condition the clinker is combustible and may be desulphurized by self sustained combustion carried on either in heaps in the open air or in stalls or kilns.
- the combustion may be checked by withdrawing the charge from the furnace before the combustion is completed and While a large part of the unconsumed fuel is retained within the mass. This mass of ore and fuel may then be smelted in a blast or other furnace without the addition of other fuel.
- Figure 1 is a side view with a portion in section on the line Y Y of Fig. 2.
- Fig. 2. is a section on the line Z Zof Fig. 1
- Fig. 3. is a section on line X X of Fig. 1.
- the furnaces A A as here shown are arranged in the form of a double bank back to back the two sets being separated by a bridge wall e.
- Each furnace is provided with a perforated grate d of ordinary construc tion.
- a is the charging door, b the ash door, and c the air blast opening beneath each grate connected with a blower or other source of supply.
- Extending above the furnaces is a fine B and there is an opening 4; at the top of each furnace through which the gases pass into the fine.
- the flue B is connected with any suitable exhaust apparatus for the purpose of creating a draft.
- a pipe f carries off the products of combustion and discharges into the end of the flue B.
- a perforated air pipe j extends along the bottom of the kiln and is connected with the blower or air supply.
- This cake is then broken up byabar and pulled out of the furnace to cool, fresh ore and coal are spread over the hearth and the operation repeated making the process continuous and rapid.
- the caked I 5 ore is firmly cemented together in a spongy form having distributed evenly through it the coked coal.
- a small proportion of the sulphur is removed, also zinc and arsenic to some extent. No silver, gold or copper is lost by the operation and but a trifling amount of lead.
- Some latitude however exists according to the object to be at tained. For instance, if it be desired to retain the sulphur, zinc, and lead, the blast is increased and the operation quickened so that the process will be completed before the sulphur has time to burn or the zinc to vaporize.
- the coke obtained at anominal cost as slack coal is a waste product of little value when compared with coke as ordinarily produced. If it is desirable to fully desulphurize the ore, then the cemented spongy mass as drawn from the furnace A is immediately (while hot) thrown into the kiln G where it ignites and burns slowly, consuming all its sulphur and coal contained in the mass until it is thoroughly desulphurized, the operation in the kiln G being perpetual, the clinkerbeing charged in at the top opening g and as fast as desulphurized drawn out at the bottom opening h.
- the perforated pipe at the bottom furnishes a small amount of air to help sustain combustion if necessary,
- the ores which work best are those which contain considerable sulphide of iron or those commonly known as sulphurets. Ores of different kinds may be mixed to form the proper charge for the furnace, but it is in all cases desirable that the ore contain at least ten per cent. of sulphide of iron, copper, or lead. For treating fine dust sulphide ores may-be mixed with it, or if it contains lead in considerable proportion, no sulphide ore is necessary. The fume arising from the combustion of the ore may be drawn off and saved, but this is not usually of much value, especially when the process is conducted with rapidity.
- the quantity of coal used in the process can be varied to suit the character of the ore. If desirable a large quantity of fuel can be used with perfect results. No benefit arises however from the introduction of much fuel if the cemented ore is to be subsequently roasted to get rid of the sulphur, but it would be desirable if it is desired to smelt the ore;
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
UNrTEn STATES PATENT FFICEQ FRANK L. BARTLETT, OFOAFION CITY, COLORADO.
PROCESS OF TREATING ORES.
! SPECIFICATION forming part of Letters Patent No. 512,531, dated January 9, 1894.
Application filed January 11, 1893. Serial No. 457,981. (No specimens.)
To all whom it may concern:
" tion of certain finely divided ores for the process of smelting in blast or other furnaces. It is well known that fine ores, or granular ores, are exceedingly difficult to smelt in blast furnaces owing to their tendency to pack in the furnace or to blow outwith the blast. Many devices have been tried for working these ores, such as making bricks or balls of the ore, or by cementing the grains together with chemicals. Besides being expensive, the bricked or balled ore falls to pieces when heat is applied and the results have not been satisfactory. In order to smelt such ores they now have to be used in small quantities at a time or else previous to smelting they have to be roasted very slowly and at great expense and partly clinkered or cemented by raising the heat at the latter end of the operation. I have'discovered a cheap process whereby such ores may be cemented quickly and cheaply by waste fuel, in sucha manner that the ore becomes combustible and may be burned to get rid of the sulphur, may be partially fused and cemented with a certain amount of fuel contained or entangled in the mass so that the ore may be smelted direct without additional fuel. Any finely divided ore may be used, such as concentrates of gold, silver, copper, zinc and lead, or flue dust and iron and copper mattes. Natural granular ores, may also be used or the ore may be crushed to pea and dust size, and then operated on. I have discovered that such material, especially that containing the sulphides of iron, copper, zinc and' lead if mixed with any slack or waste coal, and submitted to an air blast either on perforated grates or on closed hearths, may be quickly cemented or clinkered and that such material, or clinker, can be made to retain a large portion of the fuel in an available form and that in this spongy or cemented condition the clinker is combustible and may be desulphurized by self sustained combustion carried on either in heaps in the open air or in stalls or kilns.
If it is not desired to desulphurize the ore but to prepare it for subsequent smelting the combustion may be checked by withdrawing the charge from the furnace before the combustion is completed and While a large part of the unconsumed fuel is retained within the mass. This mass of ore and fuel may then be smelted in a blast or other furnace without the addition of other fuel.
I have illustrated in the accompanying drawings a set of furnaces well adapted to carry out my process.
In the drawings Figure 1. is a side view with a portion in section on the line Y Y of Fig. 2. Fig. 2. is a section on the line Z Zof Fig. 1, and Fig. 3. is a section on line X X of Fig. 1.
The furnaces A A as here shown are arranged in the form of a double bank back to back the two sets being separated bya bridge wall e. Each furnace is provided with a perforated grate d of ordinary construc tion. a is the charging door, b the ash door, and c the air blast opening beneath each grate connected with a blower or other source of supply. Extending above the furnaces is a fine B and there is an opening 4; at the top of each furnace through which the gases pass into the fine. The flue B is connected with any suitable exhaust apparatus for the purpose of creating a draft.
At the end of the furnaces A,I construct two kilns G having charge openings gg at thetop and lower doors h for withdrawing the burned'charge. A pipe f carries off the products of combustion and discharges into the end of the flue B.
A perforated air pipe j extends along the bottom of the kiln and is connected with the blower or air supply.
In operating my furnace an air blast of four to ten ounces is used and the furnaces A are first heated by an ordinary coal fire until the hearth and walls are sufficiently heated to ignite coal quickly. The operation then begins by spreading over the grate a thin layer of slack coal preferably of the coking class, then a layer of the ore to be treated, then another layer of coal and ore until it has a depth of three to five inches. The heavy blast ignites the gas of the heated coal and the sulphur of the ore, resulting in partially oxidizing the ore and coking the coal. In a few moments the mass is sufficiently heated to partially fuse, cementing the particles to- [O gether forming a cake. This cake is then broken up byabar and pulled out of the furnace to cool, fresh ore and coal are spread over the hearth and the operation repeated making the process continuous and rapid. The caked I 5 ore is firmly cemented together in a spongy form having distributed evenly through it the coked coal. At the same time a small proportion of the sulphur is removed, also zinc and arsenic to some extent. No silver, gold or copper is lost by the operation and but a trifling amount of lead. Some latitude however exists according to the object to be at tained. For instance, if it be desired to retain the sulphur, zinc, and lead, the blast is increased and the operation quickened so that the process will be completed before the sulphur has time to burn or the zinc to vaporize. Or, on the other hand,if it be desirable to remove a portion of the sulphur and zinc c the blast is lowered and the operation made slower. I have discovered that fine ores treated this way can be made to hold coke in sufficient quantity to be self smelting in the blast furnace and that ore so treated is more 3 5 easily and quickly smelted than the untreated ore. Moreover ore so treated desulphurizes to a large extent in the blast furnace, zinc is more fully eliminated, and the loss by blowing outof the furnace is largely reduced.
Moreover the coke obtained at anominal cost as slack coal is a waste product of little value when compared with coke as ordinarily produced. If it is desirable to fully desulphurize the ore, then the cemented spongy mass as drawn from the furnace A is immediately (while hot) thrown into the kiln G where it ignites and burns slowly, consuming all its sulphur and coal contained in the mass until it is thoroughly desulphurized, the operation in the kiln G being perpetual, the clinkerbeing charged in at the top opening g and as fast as desulphurized drawn out at the bottom opening h. The perforated pipe at the bottom furnishes a small amount of air to help sustain combustion if necessary,
and the flue f draws off the products of combustion. When much sulphur is present the cemented material can be burned in heaps in the open air, but the desulphurization is not so complete as when burned in the kiln described.
The ores which work best are those which contain considerable sulphide of iron or those commonly known as sulphurets. Ores of different kinds may be mixed to form the proper charge for the furnace, but it is in all cases desirable that the ore contain at least ten per cent. of sulphide of iron, copper, or lead. For treating fine dust sulphide ores may-be mixed with it, or if it contains lead in considerable proportion, no sulphide ore is necessary. The fume arising from the combustion of the ore may be drawn off and saved, but this is not usually of much value, especially when the process is conducted with rapidity.
The quantity of coal used in the process can be varied to suit the character of the ore. If desirable a large quantity of fuel can be used with perfect results. No benefit arises however from the introduction of much fuel if the cemented ore is to be subsequently roasted to get rid of the sulphur, but it would be desirable if it is desired to smelt the ore;
I claim-- 1. The herein described process of ccmenting finely divided 'ore, flue-dust, matte &c. preparatory to smelting, which consists of mixing it with slack coal and subjecting it to the action of a quick air blast in a suitable ,furnace whereby the coal is partially burned and the mineral elements melted to form a spongy coherent mass, without reduction of the metals substantially as described.
2. The herein described process of preparing finely divided ore, flue dust, matte, &c. for subsequent smelting which consists of mixing it with finely divided cokingcoal and subjecting the mixture to the action of heat and aquick airblast in a suitable furnace until the coal is coked and the mineral elements fused to cement the mass together without reduction of the metals, substantially as described.
3. The herein described process of treating finely divided ore, flue dust the. which consists of mixing it with finely divided coking coal and subjecting the mixture to the action of heat and aquick air blast in a suitable furnace until the coal is coked and the mineral elements fused to cement the mass together and subsequently smelting the ore without the addition of otherfuel, without reduction of themetals substantially as described.
4:. The herein described process of desulphurizing ores the. which consists of reducing them to a finely divided state mixing them with slack coal and subjecting the mixture to the action of a quick air blast in a suitable furnace until the coal is partially burned and the mineral elements are fused to form a spongy coherent mass, withdrawing the charge and subsequently completing the combustion of carbonaceous matter and sulphur without reduction of the metals, substantial] y as described.
In testimony whereofI affix my signature in presence of two witnesses.
FRANK L. BARTLETT.
Witnesses:
. S. W. Barns,
CHAS. P. WILLIAMS.
IIO
Publications (1)
Publication Number | Publication Date |
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US512531A true US512531A (en) | 1894-01-09 |
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US512531D Expired - Lifetime US512531A (en) | Process of treating ores |
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