US862987A - Art of treating ores. - Google Patents
Art of treating ores. Download PDFInfo
- Publication number
- US862987A US862987A US344?4406A US862987DA US862987A US 862987 A US862987 A US 862987A US 862987D A US862987D A US 862987DA US 862987 A US862987 A US 862987A
- Authority
- US
- United States
- Prior art keywords
- ore
- chlorid
- metals
- treating
- metal
- 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
- 229910052751 metal Inorganic materials 0.000 description 27
- 239000002184 metal Substances 0.000 description 27
- 150000002739 metals Chemical class 0.000 description 17
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 16
- 239000002253 acid Substances 0.000 description 16
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 11
- 229910052721 tungsten Inorganic materials 0.000 description 11
- 239000010937 tungsten Substances 0.000 description 11
- 229910052714 tellurium Inorganic materials 0.000 description 8
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 7
- 229910052783 alkali metal Inorganic materials 0.000 description 7
- 150000001340 alkali metals Chemical class 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 229910052750 molybdenum Inorganic materials 0.000 description 7
- 239000011733 molybdenum Substances 0.000 description 7
- 229910052720 vanadium Inorganic materials 0.000 description 7
- 229940045605 vanadium Drugs 0.000 description 7
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 7
- 229910052770 Uranium Inorganic materials 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- SURLGNKAQXKNSP-DBLYXWCISA-N chlorin Chemical compound C\1=C/2\N/C(=C\C3=N/C(=C\C=4NC(/C=C\5/C=CC/1=N/5)=CC=4)/C=C3)/CC\2 SURLGNKAQXKNSP-DBLYXWCISA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910000442 triuranium octoxide Inorganic materials 0.000 description 1
- -1 vans dium Chemical compound 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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
- C22B60/00—Obtaining metals of atomic number 87 or higher, i.e. radioactive metals
- C22B60/02—Obtaining thorium, uranium, or other actinides
- C22B60/0204—Obtaining thorium, uranium, or other actinides obtaining uranium
- C22B60/0217—Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes
- C22B60/0221—Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching
- C22B60/0226—Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching using acidic solutions or liquors
- C22B60/0234—Obtaining thorium, uranium, or other actinides obtaining uranium by wet processes by leaching using acidic solutions or liquors sulfurated ion as active agent
Definitions
- My invention has reference to a treatment of ores containing one or more of the acid forming rare metals tungsten, uranium, vanadium, molybdenum and tellurium which are weakly basic and acid forming in which I effeet the separation and recovery of the rare metal or metals by mixing the ore with an alkaline chlorid, preferably much in excess of the amount required to furnish chlorin for the chloridizable constituents of the ore, and heating the resulting mixture until the alkaline chlorid and rare metal or metals have reacted and'volatile and soluble chlorids or double chlorids of the alkali metal used and the rare metals in the ore have been formed.
- the ore containing tungsten as the rare metal and using sodium chlorid as the alkaline chlorid
- the ore is preferably reduced to a fine consistency, most advantageously, to about thirty (30) mesh. It is then mixed with about double the amount of ordinary commercial sodium chlorid and fed into the heating furnace, which is preferably 0f the revolving cylindrical type, feeding, agitating and discharging the ore automatically; or the ore and salt may be fed separately into the furnace and allowed to mix within it.
- suitable acid such as hydrochloric.
- the ore contains a metal whose oxid is soluble in ammonia, such as silver, copper, nickel, zinc, etc.
- a metal whose oxid is soluble in ammonia such as silver, copper, nickel, zinc, etc.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Geology (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
OFFICE.
ROBERT McKNIGHT, OF PITTSBURG, PENNSYLVANIA.
ART OF TREATING ORES.
T9 all whom it may concern:
Be it known that I, Bonsai MCKNIGH'I', a citizen of the United States, residing at the city of Pittsburg, in the county of Allegheny and State of Pennsylvania, have invented new and useful Improvemehts in the Art of Treating Ores, of which the following is a specification.
My invention has reference to a treatment of ores containing one or more of the acid forming rare metals tungsten, uranium, vanadium, molybdenum and tellurium which are weakly basic and acid forming in which I effeet the separation and recovery of the rare metal or metals by mixing the ore with an alkaline chlorid, preferably much in excess of the amount required to furnish chlorin for the chloridizable constituents of the ore, and heating the resulting mixture until the alkaline chlorid and rare metal or metals have reacted and'volatile and soluble chlorids or double chlorids of the alkali metal used and the rare metals in the ore have been formed.
I will describe now in detail the manner in which I practice my invented art.
Taking as a specific case an ore containing tungsten as the rare metal and using sodium chlorid as the alkaline chlorid, I treat it as follows The ore is preferably reduced to a fine consistency, most advantageously, to about thirty (30) mesh. It is then mixed with about double the amount of ordinary commercial sodium chlorid and fed into the heating furnace, which is preferably 0f the revolving cylindrical type, feeding, agitating and discharging the ore automatically; or the ore and salt may be fed separately into the furnace and allowed to mix within it. As to the amount of salt to be used, the more used the quicker and better are the results obtained, In practice, however, it is found that the advantages derived from the use of a large excess of the salt, such as would be expected from the law of mass action, become after a certain point counterbalanced by the disadvantage of having to handle too large a bulk of material; and hence the optimum maximum amount of, salt to be used in each case is best determined experimentally ior each ore. The temperature in most cases need not exceed 700 (3., which can be obtained through any available fuel. Where electricity is obtainable, a good furnace in which to carryout my invention is that described in my application for Letters Patent Ser. No. 332,403 filed August 28th, 1906. By this treatment the tungsten in the ore is converted into a volatile and soluble chlorid or double chlorid of the sodium and tungsten, what is volatilized is condensed in a suitable condenser, such as is described in U. S. Patent No. 737,003, August 25th, 1903; granted to me, and entitled Apparatus for condensingfumes; and the residue, preferably while hot from the furnace, is allowed to fall into water, and thus by the sudden change of the temperature quickly disintegrated and crumbled and the portion of the tungsten which has not volatilized is ob- Specification of Letters Patent. Application filed November 20,1QI1B. flsrlal -30. 844.844- 4 o Iatented Aug. 13, 1907.
tained in solution, from which its acid or the metal itself can be obtained in any suitable manner. cases it is found advantageous to let the ore which has passed through the furnace pass also through asuitable pulverizer, which is preferably done after the hot ore has been suddenly cooled by the water and thus disintegrated and made easy to crush. In this way the complete solution of the portion which has. not volatilized is insured to be effected easily .and wel I prefer also to use a limited amount of water, whichI keep in circulation through all the apparatus used, including the pulverizer, by means of a suitable pufnp, and thus I can obtain a supersaturated solution of the metal or metals in question, which on standing is precipitated, usually as the hydrated oxid or acid, and use the filtrate from this precipitate for the recovery by spontaneous evaporation Insome or otherwise the alkaline chlorid in solution, which can be used-over again in the treatment of new ore.
In some cases I prefer to precipitate the acid of the rare metal by rendering its solution acid by means ofsome suitable acid, such as hydrochloric. When the latter acid is used there is obtained the additional advantage that most of the alkaline chlorid is thrown down along with the acid of the rare metal, especially when the hydrochloric acid is led into the solution in the gaseous form, on account of the decrease in the ionization by the common anion in the solution and precipitating acid; and thus it becomes a simple matter to recover and separate the alkaline chlorid used, all that is necessary being the washing with water of the mixed rare metal acid and alkaline chlorid, obtaining the latter in the filtrate and the former as the residue on the filter.
In cases where the ore contains a metal whose oxid is soluble in ammonia, such as silver, copper, nickel, zinc, etc., I prefer 'to use as the condensing liquid for the volatilized portion and as the solvent for the residual portion a solution containing ammonia. This avoids the partial loss of rare metal by reason of the slight solubilityor insolubility of the double compounds which the oxids of the metals that are electropositive with reference to the rare metals, in some cases,
- apparently form with the oxids of the latter.
Representing by X the variable excess of alkaline chlorid used in the specific case of the tungsten ore described above, we may represent symbolically the principal reactions taking place as follows: i
Similarly in the case of an ore containing pitchblende the following equation represents the principal probable Similar and analogous equations represent the principal reaction taking place in the cases of vanadium, molybdenum and tellurium ores. Thus in the case of a vanadium ore such as vanad te, the principal reaction may be represented by the following equation:
In the case of a tellurium ore siich as tetradyinite, the principal reaction may be represented by the following equation: 7
Bi Tm-l-XbTaCl-l-QQ (the atmosphere) 2Bi0 Cl3TeOl .7Na O (X-14)Na01.
Having now described my invention what I claim and desire to secure by Letters Patent is:
'1. The art of treating ores which contain one or more of the acid forming rare metals tungsten, uranium, vana dium, molybdenum and tellurium, which consists in treating the ore with an alkali-metal chlorid and heating the resulting mixture until volatile and soluble chlorids of these metals have been formed, condensing what has been volatilized' and treating the residue with an aqueous liquid. substantially as described.
2. The art of treating ores which contain one or more of the acid forming rare metals tungsten, uranium, vans dium, molybdenum and tellurium, which consists in treating the ore with a large excess of an alkali-metal chlorid and heating the resulting mixture until volatile and soluble chlorids of these metals have been formed, condensing what is volatllized and treating theresidue with an aqueous liquid, substantially as described.
3. The art of treating ores which'contain one or more of the acid forming rare metals tungsten, uranium, vanadium, molybdenum and tellurium, which consists in treating the ore with an alkali-metal chlorid and heating the resultlng mixture until volatile and soluble chlorids of these metals have been formed, condensing what has been volatilized and passing the residual ore and the thus resulting salts while hot from the furnace into a solvent liquid, substantially as described.
4. The art of treating ores which contain one or more of the acid forming rare metals tungsten, uranium, vanadium, molybdenum and tellurium, which consists in treating the ore with an alkali-metal chlorid and heating the re sulting mixture until volatile and soluble chlorids or douhle chlorids of these metals have been formed, con- (lensing what is volatilized, passing the residue while hot from' the furnace into water, and therefrom throughin suitable pulverizer through which circulates a limited amount of the solvent for the thus resulting metallic compounds, substantially as described.
5. The art of treating ores which contain one or more of the acid forming rare metals tungsten, uranium, vanadium, molybdenum and tellurium, which consists in treating the ore with an alkali-metal chlorid and heating the resulting mixture until volatile and soluble chlorids or double chlorids of these metals have been formed, condensing what is volatilized, passing the residue while hot from the furnace into water, and thereafter through a suitable pulverizer through which circulates the solvent for the thus resulting metallic compounds, using the same solution ovr and over again until it becomes super-sat urated and deposits the less soluble rare metal compounds, thus leaving the alkali metal chlorid in solution, which can be used in the treatment of new ore, substantially as described. a
In witness whereof I aflix my signature in presence of two witnesses.
ROBERT MCKNIGHT.
Witnesses:
WALTER S. BUTLER, B. C. BARTON.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US862987TA |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US862987A true US862987A (en) | 1907-08-13 |
Family
ID=2931438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US344?4406A Expired - Lifetime US862987A (en) | Art of treating ores. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US862987A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2576101A (en) * | 1948-04-17 | 1951-11-27 | Climax Uranium Company | Method for treatment of vanadium and uranium ores |
| US3429671A (en) * | 1965-05-26 | 1969-02-25 | Nuclear Materials & Equipment | Method of treating carbon containing material |
-
0
- US US344?4406A patent/US862987A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2576101A (en) * | 1948-04-17 | 1951-11-27 | Climax Uranium Company | Method for treatment of vanadium and uranium ores |
| US3429671A (en) * | 1965-05-26 | 1969-02-25 | Nuclear Materials & Equipment | Method of treating carbon containing material |
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