US509058A - Elwyn waller and charles augustus sniffin - Google Patents
Elwyn waller and charles augustus sniffin Download PDFInfo
- Publication number
- US509058A US509058A US509058DA US509058A US 509058 A US509058 A US 509058A US 509058D A US509058D A US 509058DA US 509058 A US509058 A US 509058A
- Authority
- US
- United States
- Prior art keywords
- lead
- ore
- sniffin
- elwyn
- acetic acid
- 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 42
- 238000000034 method Methods 0.000 description 17
- 239000000243 solution Substances 0.000 description 13
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 11
- 229910052709 silver Inorganic materials 0.000 description 11
- 239000004332 silver Substances 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 229940046892 lead acetate Drugs 0.000 description 8
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 7
- 229910000003 Lead carbonate Inorganic materials 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- 150000001242 acetic acid derivatives Chemical class 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000010970 precious metal Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- -1 real or combined Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- 229910001958 silver carbonate Inorganic materials 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 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
- C22B11/00—Obtaining noble metals
- C22B11/04—Obtaining noble metals by wet processes
Definitions
- acetic acid be used in a proportion greater than one hundred and twenty pounds of real acid to two hundred and seven pounds of lead as carbonate in the ore, and if, as may sometimes occur, the ore contains silver carbonate, some silver acetate may be formed and go into solution. In such a case the silver may be put back into the undissolvedresidue' by the addition to the charge of a small amount of metallic lead in a subdivided condition. The action which takes place is the substitution of lead for the silver in the solution, the silver separating out in the metallic state. The carbonic acid evolved in the process will be collected and utilized, and in order to recover this acid the process is carried on out of contact with the air.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Description
UNITED STATES PATENT OFFICE.
' ELWYN VVALLER AND CHARLES AUGUSTUS SNIFFIN, OF NElV YORK, N. Y.
METHOD OF CONCENTRATING oREs.
SPECIFIGATIONforming part of Letters Patent No. 509,058, dated November 21, 1893. Application filed May 2, I893. Serial No.472.787. (No specimens.)
To aZZ whom it may concern:
Be it known that we,-ELWYN WALLER and OHARLns AUGUSTUS SNIFFIN, both citizens of the Unlted States, and residents of the city, county, and State of New York, have invented certain new and useful Improvements in Methods. of Concentrating Ores, of which the following is a specification.
The methods ordinarily employed for concentrating ores depend chiefly or entirely upon the difierence of specific gravity between the ore or free metal and the gangue with WhlOll the ore is associated, whereby, when the finely pulverized material is agitated with air or water, or by some mechanical means, the material having the higher specific gravity is conveyed to or deposited in one place, while the portion having the lower speclfic gravity is conveyed to or deposited in another place. Thus a rough sort of separatlon 1s effected. and the major portion of the gangue disposed of. These methods are designed to separatethe metal-bearing ore or free metal from the gangue or rock, and not to separate one metal in the ore from another metal contained therein. Some ores are found vto contain both a base metal and a precious metal, the percentage of baser metal being usually much the larger, and in order to concentrate the precious metal, it is desirable to remove the baser metal from the crude ore or material. Our invention has reference more especlally to this latter class of concentration. Our method of concentrating has for its obect to remove from the ore certain portions thereof which portions are brought into solution, thus affording compounds valuable in the arts, while other portions of the valuable material are thus concentrated in the residue or undissolved gangue. This method may be employed either separately, or in conjunction with some other method or methods of separation and concentration, dependent upon specific gravity alone.
With the carbonate ores of lead, containing the mineral cerussite more or less mixed with other minerals, we are able by our process, when silver is present, to dissolve out the lead and leave the silver in the residue with the other undissolved substances, the result belng aconcentration of the silver in such argentiferous ores. It may be desirable to remove all of the lead, or to leave a portion of the lead with the silver in the residue from the concentration, in order to facilitate the extraction of the silver present; and the proportion of lead left in the residue may be regulated either by the strength of the solvent solution used, or by the length of time which said so lution is permitted to act, or by the proportion of the solvent to the amount of ore treated,or by the character of the solvent employed.
The solvents we have found very effective are acetic acid and solutions of acetate of lead. Practically all acetates, as well as acetic acid, when in aqueous solution, will, with the aid of heat, dissolve out the lead from lead carbonate ores. The action of all is the same .in kind but different in degree.
Our process may be carried out by mixing together in a suitable vessel acetic acid,water and argen tit'erous ore containing lead carbonate, and heating this mixture up to the point of ebullition. The acetic acid combines with the lead, forming lead acetate, and gaseous carbonic acid is set free. The solution of lead acetate is drawn off and the argentiferous residue reserved for treatment by any known process for the extraction of the silver.
It will be obvious that no exact proportions of the several ingredients can beprescribed, nor are any exact proportions essential: If the proportion of acid is equal to or greater than one hundred and twenty pounds of real acetic acid to two hundred and seven pounds of lead, as carbonate, in the ore, neutral lead acetate will be formed and will pass into solution. If the proportion of lead in the ore is greater than that given above, basic lead acetates will be formed by the action of the neutral acetate upon the lead carbonate remaining. This action is somewhat slower than when acetic acid is used, but at a boiling temperature the action is rapid, becoming gradually slower as the solution becomes more and more basic.
When a solution of the neutral lead acetate is subjected to prolonged boiling, some of the acetic acid passes on with the steamand watery vapor and may be condensed and utilized again as a solvent for concentration, on a fresh lot of ore. By this treatment the solotion is converted into a solution of basic lead acetate.
If acetic acid be used in a proportion greater than one hundred and twenty pounds of real acid to two hundred and seven pounds of lead as carbonate in the ore, and if, as may sometimes occur, the ore contains silver carbonate, some silver acetate may be formed and go into solution. In such a case the silver may be put back into the undissolvedresidue' by the addition to the charge of a small amount of metallic lead in a subdivided condition. The action which takes place is the substitution of lead for the silver in the solution, the silver separating out in the metallic state. The carbonic acid evolved in the process will be collected and utilized, and in order to recover this acid the process is carried on out of contact with the air.
The action of other acetates than lead acetate, at the boiling temperature, will be to form, chiefly, neutral lead acetate; a portion of the carbonic acid from the carbonate ore is driven off with the steam and a portion combines with the base of the acetate employed to form a carbonate.
We do not claim the manufacture of acetates bysprinkling the ground ore with acetic acid and exposing them to the air, nor do We claim the recovery of metals from ores by the combined action of the oxidizing influence of air and thatof acetic acid. Our process excludes the air and has for its object the'con centration of the precious metal in the residue by the extraction of the baser metal, lead.
Having thus described our invention, we clai-m-- 1. The herein described method of concentrating argentiferous lead carbonate ores which consists in dissolving out lead from the ore with the aid of acetic acid, real or combined, and water, out of contact with the air whereby the lead and carbonic acid elimi- 'nated from the ore are rendered capable of utilization in the arts, and the undissolved silver is concentrated in the residue, substantially as set forth.
2. The herein described method of concentrating argentiferous lead carbonate ores which consists in removing the lead, or the major portion thereof, from the one with the aid of water, acetic acid and heat, and out of contact with the air whereby the undissolved silver is concentrated in the residue, substantially as set forth.
3. In the treatment of lead carbonate ores, the method of recovering acetic acid from neutral acetate solutions, which consists in boiling the solution, whereby it is converted into a solution of basic lead acetate, and condensing the vaporized acetic acid,.substantially as set forth. I
In witness whereof we have hereunto signed our names in the presence of two subscribing witnesses.
' ELWYN WALLER.
CHARLES AUGUSTUS SNIFFIN.
Witnesses:
HERBERT BLossoM, J AS. KING DUFFY.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US509058A true US509058A (en) | 1893-11-21 |
Family
ID=2577887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US509058D Expired - Lifetime US509058A (en) | Elwyn waller and charles augustus sniffin |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US509058A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2839390A (en) * | 1954-07-23 | 1958-06-17 | Torrence D Galloway | Cyclic process of extracting lead and zinc metals |
| US5523066A (en) * | 1994-06-08 | 1996-06-04 | Centaur Mining Exploration Limited | Treatment of lead sulphide bearing minerals |
-
0
- US US509058D patent/US509058A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2839390A (en) * | 1954-07-23 | 1958-06-17 | Torrence D Galloway | Cyclic process of extracting lead and zinc metals |
| US5523066A (en) * | 1994-06-08 | 1996-06-04 | Centaur Mining Exploration Limited | Treatment of lead sulphide bearing minerals |
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