US52834A - Improved process for separating gold and silver from ores - Google Patents
Improved process for separating gold and silver from ores Download PDFInfo
- Publication number
- US52834A US52834A US52834DA US52834A US 52834 A US52834 A US 52834A US 52834D A US52834D A US 52834DA US 52834 A US52834 A US 52834A
- Authority
- US
- United States
- Prior art keywords
- ores
- silver
- sulphurets
- improved process
- gold
- 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
- 238000000034 method Methods 0.000 title description 34
- 229910052709 silver Inorganic materials 0.000 title description 16
- 239000004332 silver Substances 0.000 title description 16
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 title description 12
- 229910052737 gold Inorganic materials 0.000 title description 12
- 239000010931 gold Substances 0.000 title description 12
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 235000011149 sulphuric acid Nutrition 0.000 description 12
- 239000001117 sulphuric acid Substances 0.000 description 12
- 238000000354 decomposition reaction Methods 0.000 description 10
- 239000010970 precious metal Substances 0.000 description 10
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 10
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 8
- 229910052753 mercury Inorganic materials 0.000 description 8
- 238000005267 amalgamation Methods 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N Potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 4
- VWDWKYIASSYTQR-UHFFFAOYSA-N Sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
- 239000005864 Sulphur Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 150000002823 nitrates Chemical class 0.000 description 4
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052904 quartz Inorganic materials 0.000 description 4
- 239000010453 quartz Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 241001272996 Polyphylla fullo Species 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 230000001264 neutralization Effects 0.000 description 2
- 230000001590 oxidative Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000010333 potassium nitrate Nutrition 0.000 description 2
- 238000003303 reheating Methods 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 235000002639 sodium chloride Nutrition 0.000 description 2
- 159000000000 sodium salts Chemical class 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
- C22B11/00—Obtaining noble metals
- C22B11/08—Obtaining noble metals by cyaniding
Definitions
- the object of our invention is to effect the decomposition of sulphurets containing gold and silver, and thereby to free the precious metals contained therein, so as to be acted upon by subsequent processes of amalgama tion, and to accomplish this decomposition by means so economical as to effect a great saving over any processes heretofore used.
- Auriferous or argentiferous sulphurets, or ores containing such sulphurets, after being removed from the mine, are broken into lumps of convenient size, and are subjected to any known process of roasting, which may be effected in reverberatory furnaces or in kilns, or by heaping the ore with combustibles upon logs so that a free current of air shall pass through the ignited pile. It is advisable that the temperature to which the ores are subjected shall be as nearly as possible that of a dull red heat.
- the pyrites containing the precious metals are partially oxidized, the sulphurets being more or less converted into sulphates.
- WVe next take the roasted ore while still at a high temperature and immerse it in a bath composed of a strong solution of nitrate of potash or nitrate of soda; but we prefer crude nitrate of soda, as being more economical.
- This solution may be contained in suitable vats, and successive portions of the ore may be treated with the same solution.
- a decomposition of the nitrate takes place.
- the sulphuric acid of the sulphate contained in the heated ores having a higher affinity for the alkali than for the bases with which it was before combined, leaves these bases and combines with the alkali of the nitrate, forming a sulphate of the alkalie.
- a sulphate of soda or potash which remains neutral, performing no part in the required decomposition. Free nitric acid in excess is disengaged.
- a portion of the oxygen of the nitric acid so produced combines with the metallic bases, such as the iron,copper, and silver, forming oxides of the metals, and another portion of the oxygen combines with the sulphur of the sulphurets, converting it into sulphuric acid, which, uniting with the oxides of the metals, forms sulphates-c. g., sulphates of iron, copper, and silver.
- These reactions separate, divide,and decompose the sulphurets, rendering them friable and exposing the precious metals.
- the sulphurets are mixed with quartz the latter is also made friable by the same process. This process should be repeated until entire decomposition is effected.
- the object is the treatment of gold ores for amalgamation, it will be necessary to remove the sulphuric acid from the sulphates formed as above. This may be done by exposing the ores which have passed through the process above described to a full red heat, when the sulphuric acid will distill oft'and leave the oxides of the base metals and fully expose the particles of gold to the action of the mercury in the amalgamating process.
- the ores will be sufficiently decomposed by the process above described to be subjected to the usual processes of amalgamation, either in amalgamating-pans with mullers or in arastra mills.
- the reheating process is dispensed with.
- the ore containing the sulphates is in a condition to decompose the chloride of sodium or sea-salt to which it is subjected by Well-known processes for the formation of chloride of silver, which yields its silver readily to the mercury.
- the process of oxidizing sulphurets containin g the precious metals and converting them into sulphates by the use of solutions of nitrates, for the purpose and in the manner substantially as above described.
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
UNTTnn STATES PATENT FFEQEQ JOHN 'H. ELWVARI), OF POLO, ILL., AND JOHN L. HAYES, OF BOSTON, MASS.
IMPROVED PROCESS FOR SEPARATING GOLD AND SILVER FROM ORES.
Specification forming part of Letters Patent No. 52,534, dated February 27, 1866.
To all whom it may concern:
Be it known that we, JOHN H. ELWARD, of Polo, in the county of Ogle and State of Illinois, and JOHN L. HAYES, of Boston, in the countyof Suffolk and Common wealth of Massaehusetts, have invented a new and Improved Process for Extracting the Precious Metals from sulphurets and Ores containing Sulphurets; and we do hereby declare that the followingis a full and exact description thereof.
It is well known that free gold, such as is found mixed with earthy deposits in placerdiggings or is combined with quartz after the same has been crushed, is readily separated by the action of mercury, and it is also well known that gold is often included in exceedingly fine particles within sulphurets of iron and copper, and being thus shielded from contact with mercury cannot be perfectly amalgamated.
The object of our invention is to effect the decomposition of sulphurets containing gold and silver, and thereby to free the precious metals contained therein, so as to be acted upon by subsequent processes of amalgama tion, and to accomplish this decomposition by means so economical as to effect a great saving over any processes heretofore used.
To enable others skilled in metallurgical arts to use our invention, we will proceed to describe its operation.
Auriferous or argentiferous sulphurets, or ores containing such sulphurets, after being removed from the mine, are broken into lumps of convenient size, and are subjected to any known process of roasting, which may be effected in reverberatory furnaces or in kilns, or by heaping the ore with combustibles upon logs so that a free current of air shall pass through the ignited pile. It is advisable that the temperature to which the ores are subjected shall be as nearly as possible that of a dull red heat. By this process the pyrites containing the precious metals are partially oxidized, the sulphurets being more or less converted into sulphates. We are aware that this portion of the process is well known, and we do notclaim it as any part of ourinvention. WVe next take the roasted ore while still at a high temperature and immerse it in a bath composed of a strong solution of nitrate of potash or nitrate of soda; but we prefer crude nitrate of soda, as being more economical. This solution may be contained in suitable vats, and successive portions of the ore may be treated with the same solution. We do not limit ourselves 'to this mode of applying the solution of nitrates aforesaid to the heated ores, as the application may be made to the ores by sprinkling or drenching. By bringing the heated ores into contact with the solution aforesaid a decomposition of the nitrate takes place. The sulphuric acid of the sulphate contained in the heated ores, having a higher affinity for the alkali than for the bases with which it was before combined, leaves these bases and combines with the alkali of the nitrate, forming a sulphate of the alkalie. a sulphate of soda or potashwhich remains neutral, performing no part in the required decomposition. Free nitric acid in excess is disengaged. A portion of the oxygen of the nitric acid so produced combines with the metallic bases, such as the iron,copper, and silver, forming oxides of the metals, and another portion of the oxygen combines with the sulphur of the sulphurets, converting it into sulphuric acid, which, uniting with the oxides of the metals, forms sulphates-c. g., sulphates of iron, copper, and silver. These reactions separate, divide,and decompose the sulphurets, rendering them friable and exposing the precious metals. Where the sulphurets are mixed with quartz the latter is also made friable by the same process. This process should be repeated until entire decomposition is effected.
If the object is the treatment of gold ores for amalgamation, it will be necessary to remove the sulphuric acid from the sulphates formed as above. This may be done by exposing the ores which have passed through the process above described to a full red heat, when the sulphuric acid will distill oft'and leave the oxides of the base metals and fully expose the particles of gold to the action of the mercury in the amalgamating process. The ores will be sufficiently decomposed by the process above described to be subjected to the usual processes of amalgamation, either in amalgamating-pans with mullers or in arastra mills. If the object is to prepare argentiferous ores, it being necessary to retain the sulphur in the form of sulphuric acid combined with the silver andbase metals, the reheating process is dispensed with. The ore containing the sulphates is in a condition to decompose the chloride of sodium or sea-salt to which it is subjected by Well-known processes for the formation of chloride of silver, which yields its silver readily to the mercury. In
" other words, sulphuric acid is left in the pro- What we claim as our invention, and desire to secure by Letters Patent, is'
The process of oxidizing sulphurets containin g the precious metals and converting them into sulphates by the use of solutions of nitrates, for the purpose and in the manner substantially as above described.
JOHN H. ELWARD. JOHN L. HAYES.
\Vitnesses to the signature of John L. Hayes: FRANCIS G. DYER, BYRON RosE.
Witnesses to the signature of John'H. El-
Ward:
WM. H. LORD, J. I. PEYTON.
Publications (1)
Publication Number | Publication Date |
---|---|
US52834A true US52834A (en) | 1866-02-27 |
Family
ID=2122380
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US52834D Expired - Lifetime US52834A (en) | Improved process for separating gold and silver from ores |
Country Status (1)
Country | Link |
---|---|
US (1) | US52834A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5096486A (en) * | 1990-12-13 | 1992-03-17 | Sunshine Precious Metals Incorporated | Treatment of metal bearing mineral material |
-
0
- US US52834D patent/US52834A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5096486A (en) * | 1990-12-13 | 1992-03-17 | Sunshine Precious Metals Incorporated | Treatment of metal bearing mineral material |
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