US45048A - Improved mode of preparing ores - Google Patents
Improved mode of preparing ores Download PDFInfo
- Publication number
- US45048A US45048A US45048DA US45048A US 45048 A US45048 A US 45048A US 45048D A US45048D A US 45048DA US 45048 A US45048 A US 45048A
- Authority
- US
- United States
- Prior art keywords
- ore
- ores
- salt
- improved mode
- metals
- 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
- 150000003839 salts Chemical class 0.000 description 22
- 239000011780 sodium chloride Substances 0.000 description 22
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- 150000002739 metals Chemical class 0.000 description 16
- 238000005267 amalgamation Methods 0.000 description 12
- 239000011449 brick Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 238000001354 calcination Methods 0.000 description 10
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 10
- 229910052737 gold Inorganic materials 0.000 description 10
- 239000010931 gold Substances 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 6
- 235000015450 Tilia cordata Nutrition 0.000 description 6
- 235000011941 Tilia x europaea Nutrition 0.000 description 6
- 235000012970 cakes Nutrition 0.000 description 6
- 150000003841 chloride salts Chemical class 0.000 description 6
- 239000000428 dust Substances 0.000 description 6
- 239000004571 lime Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 4
- 238000004166 bioassay Methods 0.000 description 4
- MJBPUQUGJNAPAZ-AWEZNQCLSA-N butin Chemical compound C1([C@@H]2CC(=O)C3=CC=C(C=C3O2)O)=CC=C(O)C(O)=C1 MJBPUQUGJNAPAZ-AWEZNQCLSA-N 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
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
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/04—Dry methods smelting of sulfides or formation of mattes by aluminium, other metals or silicon
Definitions
- My invention consists in taking tailings or crushed ore as it comes from the stamps or mills and mixing it with a solution of chloride of sodium or its equivalent in such proportions as to form a stiff paste,and then form or press it into cakes, lumps, or hiicks, which, after drying by exposure to the air, are calcined in a common stove, furnace, heap,or kiln'constructed so as to have a draltof heated air through the interstices of the cakes, lumps,or bricks in such a manner as to bring thechemical into the most intimate contact with every particle of the crushed ore, and admit of the subsequent calcination in the best and cheapest manner.
- Ore prepared in this manner is not only desulphurized in the best manner without the trouble and expense of building reverberatory furnaces, and the loss of dust by constantstirring or violent agitation in a current of air, but it contains all the metals, except gold, in the condition of chlorides, and when these are dissolved or decomposed the gold, if any is present,is left clear and bright and in the best possible condition for amalgamation.
- Arsenic, zinc, and antimony are the most troublesome metals in ores submitted to amalgamation; but by this process of preparingthe ore these metals are removed as volatile and soluble chlorides during the calciuation and subsequent amalgamation, and when the last operation is performed in close vessels, or by the barrel process,with metallic iron and m'ercury the chloride of silver is reduced to metallic silver and saved, and more gold may thus be obtained than by any other processot' amalgamation; but by any process of amalgamation more gold can be obtained from the prepared ore than from crude ore or roasted ore when calcined or roasted alone.
- Al'teramalgamaringor washing theprepared ore the failings may be concentrated to oneor two per cent. of its former weight, and, if do sirable, this may be smelted for nickel matte, or metallic lead, if these metals are present; but I prefer to dress or concentrate the tailings in such a manner as to leave about onefourth (more or less) of the original weight of the ore, and, after draining the concentrated residue or dressed ore, to mix this with sufficient crude ore and solution of salt to make the original quantity, and calcine, wash, or amalgamate as before, and so on continuously.
Landscapes
- 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
I UNITED STATES PATENT OEEICE.
EDWARD N. KENT, OF NEWV YORK, N. Y.
IMPROVED MODE OF PREPARING ORES.
Specification forming part of Letters Patent No. 15,048, dated November 15, 1864.
To all whom it may concern Be it known that I, EDWARD N. KENT, of the United States Assay Office, in the city, county, and State ofNewYork,haveinvented a new and useful Improvement in the Preparation of Ores; and I do hereby declare that the following is a full, clear, and exact description thereof, which will enable those skilledin the art to fully understand and use the same.
My invention consists in taking tailings or crushed ore as it comes from the stamps or mills and mixing it with a solution of chloride of sodium or its equivalent in such proportions as to form a stiff paste,and then form or press it into cakes, lumps, or hiicks, which, after drying by exposure to the air, are calcined in a common stove, furnace, heap,or kiln'constructed so as to have a draltof heated air through the interstices of the cakes, lumps,or bricks in such a manner as to bring thechemical into the most intimate contact with every particle of the crushed ore, and admit of the subsequent calcination in the best and cheapest manner.
I am aware that dry salt has been used for calcination in a reverberatory furnace; butin this case a great deal of manual labor is required at the furnace, and by constant stirring a large amount of dust is lost. The salt and ore cannot be so intimately mixed, the chemical action is less perfect, and the quantity of ore operated upon is limited to the capacity of the furnace, which is very expensive.
I am also aware that water has been used for making a paste of certain ores with lime or clay for smelting; but I am not'aware that salt and water together, or a solution of salt, has been before used for the purposes herein specified.
By the use of a solution of salt and by caking the ore a common stove, furnace, or kiln, such as is usedfor burning lime or bricks, may be used for the calcination of crushed ores or tailings; or the caked ore may be calcined in heaps. No manual labor or stirringis required during the calcination, and consequently no dust. is lost. The mixture of the salt and ore is perfect,and the quantity operatedupon may be almost unlimited, as in a limekiln the pro cess ofcalcination is continuous, and a brickkiln of ordinary dimensions containing five hundred thousand bricks of five pounds each would equal one thousand two hundred and fifty tons of ore to be calcined at one operation. It is estimated that one cord of wood is sufficient fuel for two thousand bricks or five tons of ore, and that ten thousand bricks or twenty-five tons of ore can be prepared with one machine per day.
Ore prepared in this manner is not only desulphurized in the best manner without the trouble and expense of building reverberatory furnaces, and the loss of dust by constantstirring or violent agitation in a current of air, but it contains all the metals, except gold, in the condition of chlorides, and when these are dissolved or decomposed the gold, if any is present,is left clear and bright and in the best possible condition for amalgamation.
Arsenic, zinc, and antimony are the most troublesome metals in ores submitted to amalgamation; but by this process of preparingthe ore these metals are removed as volatile and soluble chlorides during the calciuation and subsequent amalgamation, and when the last operation is performed in close vessels, or by the barrel process,with metallic iron and m'ercury the chloride of silver is reduced to metallic silver and saved, and more gold may thus be obtained than by any other processot' amalgamation; but by any process of amalgamation more gold can be obtained from the prepared ore than from crude ore or roasted ore when calcined or roasted alone.
By washing pyritic ores prepared by this process an acid solution of nickel, copper,zinc, or iron, according to the nature of the ore, together With sulphate of soda and other salts, is obtained, from which the metals may be precipitated by soda, lime, iibmsulphureted hydrogen or sulphide of sodium; or the solution may be evaporated at once to dryness, and from the chlorides thus obtained the metals, or any other compound of the metals, may be prepared without difficulty and with less expense than by the use of acids.
Al'teramalgamaringor washing theprepared ore the failings may be concentrated to oneor two per cent. of its former weight, and, if do sirable, this may be smelted for nickel matte, or metallic lead, if these metals are present; but I prefer to dress or concentrate the tailings in such a manner as to leave about onefourth (more or less) of the original weight of the ore, and, after draining the concentrated residue or dressed ore, to mix this with sufficient crude ore and solution of salt to make the original quantity, and calcine, wash, or amalgamate as before, and so on continuously.
In this way the valuable metals and the im-,
purities in the native ores are gradually separated, and the concentrated residue becoming constantly richer at every subsequent concentration, the quantity of gold which may be obtained by close amalgamation from ores prepared by this process averages from seventyfive per cent. to the full assay value of the ore.-
Having thus described my invention, I claim asnew and desire to secure by Letters Patent 1. The preparation of crushed or pulverized ores and tailings by caking them with a solution of chloride of sodium, or salt and water, introduced in any manner, so as to admit of forming the crushed ore into cakes, lumps, or bricks, as specified.
2. The calcination of crushed ores and tailings in a common stove, furnace, heap,orkiln when previously prepared by the use of a solution of chloride of sodium, or salt and water, and made into lumps of any form, so as to admit of thedecomposition of the salt by the passage of a current of heated air through the interstices of the lumps so formed, substantially as herein described.
EDWARD N. KENT. Witnesses:
M. M. LIVINGSTON, I. P. HALL.
Publications (1)
Publication Number | Publication Date |
---|---|
US45048A true US45048A (en) | 1864-11-15 |
Family
ID=2114611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US45048D Expired - Lifetime US45048A (en) | Improved mode of preparing ores |
Country Status (1)
Country | Link |
---|---|
US (1) | US45048A (en) |
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0
- US US45048D patent/US45048A/en not_active Expired - Lifetime
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