US579872A - Ceaft - Google Patents
Ceaft Download PDFInfo
- Publication number
- US579872A US579872A US579872DA US579872A US 579872 A US579872 A US 579872A US 579872D A US579872D A US 579872DA US 579872 A US579872 A US 579872A
- Authority
- US
- United States
- Prior art keywords
- pan
- ore
- shoes
- chlorin
- charge
- 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
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- 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 12
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 11
- 229910052753 mercury Inorganic materials 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 6
- 229910052737 gold Inorganic materials 0.000 description 6
- 239000010931 gold Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 239000000615 nonconductor Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229910000497 Amalgam Inorganic materials 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000005267 amalgamation Methods 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 101150006573 PAN1 gene Proteins 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000007705 chemical test Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical compound [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 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
- 238000003756 stirring Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/90—Selection of catalytic material
- H01M4/92—Metals of platinum group
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/20—Electrolytic production, recovery or refining of metals by electrolysis of solutions of noble metals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Definitions
- JOSEPH HENRY IIAYORAFT OF ADELAIDE, SOUTH AUSTRALIA, ASSIGNOR TO THE I-IAYORAFTS GOLD EXTRACTION COMPANY, LIMITED, OF SAME PLACE.
- the stirrer is so arranged that it can be actuated at any desired speed and can be raised or lowered as required by the class of ore under treatment or for the discharge of the contents of the pan. Suitable connections are made with a dynamo-electric machine, the pan being made the cathode and the stirrer with its arms the anode.
- the shoes forming the positive poles of the bath are close to the cathode and revolve below the body of the ore-pulp under treatment and do not meet toward the center, so that the well of mercury at :0 is left undisturbed and unmixed with the ore-pulp.
- M yimproved process is as follows A charge of finely-divided ore hax ing been placed in the pan is covered with water, preferably hot, to any desired depth, according to the size of the charge. I find in practice that with a charge of about one ton a depth of three to six inches well answers the purpose. Mercury is added equal to about five per cent. of the weight of the charge of ore, but varying in quantity according to the nature and quality of ore under treatment; also, about one per cent. of chlorid of sodium and about one-eighth per cent. of chlorid of barium. I may use, however any other suitable'soluble salts capable of yielding ehlorin by electrolysis.
- the sodium chlorid may be replaced by chlorid of lime.
- the temperature of the contents of the pan is raised until the water commences to boil gently, and about this temperature is maintained during the operation.
- the stirrer is caused to revolve slowly, but at such sufficient speed as will prevent the ore from settling into a hard mass.
- the dynamo being connected so as to make the pan the oathode and the stirrer with its arms the anode, a current of electricityis passed continuously through the charge of sufficient intensity to decompose the soluble salt and cause it to yield chlorin.
- the mercury being the cathode
- the chlorid of gold is decomposed by electrolysis and deposited in metallic form on the particles of mercury, by which it is at once amalgamated.
- the amalgam as formed descends to the bottom of the pan, where the mercury seizes upon any particles of coarse gold which may descend by gravitation to the bottom of the charge.
- the black coating which gradually forms on the bottom of the pan around the mercurywell consists, mainly, of iron oxid, as proved by chemical tests. That it is practically a non-conductor of electricity is shown by the fact that the chlorin set free on the carbon shoes escapes as chlorin. This is proved by working the pan without any charge of ore in it and with only sufficient salt water in the pan to cover the carbon shoes. The gas then escapes at once and has been proved to be chlorin. If the black coating had been a good conductor of electricity, hydrogen would have been set free and, combining with the chlorin, would form hydrochloric acid. This is not found to be the case. Hence the black oxid is a non-conductor.
- thciron of the pan is naturally an electropositive metal, while the carbon shoes are electronegative. If now while the dynamo is cut off from the pan a connection is made by a wire from the pan to the shoes and a galvanometer placed in circuit, a reverse current will at once be shown-i. e., the pan has become the anode and the shoes the cathode.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Electrolytic Production Of Metals (AREA)
Description
(No Model.) 1
J. H. HAYGRAPT. PROCESS OF TREATING AURIPEROUS AND ARGENTIFEROUS DRES- No. 579,872. Patented Mar; 30,1897.
JOSEPH HENRY IIAYORAFT, OF ADELAIDE, SOUTH AUSTRALIA, ASSIGNOR TO THE I-IAYORAFTS GOLD EXTRACTION COMPANY, LIMITED, OF SAME PLACE.
PROCESS OF TREATING AURIFEROUS AND ARGENIiFl-IROUS ORES.
SPECIFICATION forming part of Letters Patent No, 579,872, dated March 30, 1897.
Application filed September 29, 1894.
To (LZZ whom it may concern.-
Be it known that I, JOSEPH HENRY HAY- CRAFT, metallurgical chemist, a subject of the Queen of Great Britain, and a resident of Adelaide,in the Province of South Australia, have invented a certain new and useful Improved Process of Treating Auriferous and Argentiferous Ores, of which the following is a specification.
My invention relates to an improved process of extracting gold and silver from certain finely-divided auriferous and argentiferous ores.
It consists, essentially, in a combination at same vessel of certain known processes of electrolytic chlorination and electro-amalgamation which have previously only been worked in separate combinations or in separate vessels.
I propose .to describe my invention with reference to auriferous ores, but consider it equally suitable for certain classes of argentiferous ores.
In order that my invention maybe the better understood, I will first describe the apparatus in which it is preferably to be carried into effect, though wishing it to be distinctly un derstood that I make no claim for the apparatus as part of my invention.
The accompanying drawingshows a pan in section with my furnace and stirrer combined therewith.
This apparatus consists of a circular iron pan 1 with a rounded bottom heated by a furnace 2, the pan being preferably so arranged as to be capable of being tilted for the discharge of its contents. IVithin the pan I provide a revolving stirrer 8, having four or more arms projecting downward and each terminating in a shoe or block 4:, the shoes being arranged so as not to meet in the center of the pan. The shoes or blocks are formed, preferably, of carbon, and are shaped to the contour of the bottom of the pan, so that the whole of the lower face of the block or shoe is as near as may be equidistant from the inside of the pan, with an intervening space of about a quarter of an inch or more, as required. I do not confine myself to any partieula-r intervening space, but find in practice one and the same time and in one and the,
Serial No. 524,463. (No specimens.)
that within certain limits the nearer the anodes are to the cathode the better the result. The stirrer is so arranged that it can be actuated at any desired speed and can be raised or lowered as required by the class of ore under treatment or for the discharge of the contents of the pan. Suitable connections are made with a dynamo-electric machine, the pan being made the cathode and the stirrer with its arms the anode.
The electrical connections are shown at G 7, one of which extends down through the stirrer-arm.
The shoes forming the positive poles of the bath are close to the cathode and revolve below the body of the ore-pulp under treatment and do not meet toward the center, so that the well of mercury at :0 is left undisturbed and unmixed with the ore-pulp.
M yimproved process is as follows A charge of finely-divided ore hax ing been placed in the pan is covered with water, preferably hot, to any desired depth, according to the size of the charge. I find in practice that with a charge of about one ton a depth of three to six inches well answers the purpose. Mercury is added equal to about five per cent. of the weight of the charge of ore, but varying in quantity according to the nature and quality of ore under treatment; also, about one per cent. of chlorid of sodium and about one-eighth per cent. of chlorid of barium. I may use, however any other suitable'soluble salts capable of yielding ehlorin by electrolysis. Thus if the ore contains a large proportion of pyrites the sodium chlorid may be replaced by chlorid of lime. The temperature of the contents of the pan is raised until the water commences to boil gently, and about this temperature is maintained during the operation. In the meantime the stirrer is caused to revolve slowly, but at such sufficient speed as will prevent the ore from settling into a hard mass. The dynamo being connected so as to make the pan the oathode and the stirrer with its arms the anode, a current of electricityis passed continuously through the charge of sufficient intensity to decompose the soluble salt and cause it to yield chlorin. I find in practice that a current of about two hundred amperes at an intensity of about three volts well answers the purpose with a charge of, say, one ten, but do not confine myself to any particular current. The operation is continued for about one hour, but dependent upon the class of ore under treatment, water being added from time to time to replace that lost by evaporation. The pan is then tilted and the contents removed into a separator. The mercury recovered maybe used over and over again with fresh quantities of ore untilit is judgedto be sufticiently charged with gold to render it desirable to separate'the amalgam in the usual way.
It must be well understood that the proportions of mercury and of the soluble salts are to be varied according to the class of ore undcr treatment and that the figures given are only approximate, though found to well answer the desired purpose.
The chemical reactions which take place ap' pear to be as follows: 011 the electric current being applied chlorin is set free by electrolysis upon the carbon blocks or shoes of the stirrer, and owing to the position of these the chlorin is forced to permeate the whole mass in rising to the surface of the charge. The chlorin, being in a nascent state, acts rapidly on the minute particles of gold with which it comes in contact and forms with them chlorid of gold. At the same time the mercury at the bottom of the pan under the action of the heat rises, and, assisted by the action of the stirrer, permeates the charge. The mercury being the cathode, the chlorid of gold is decomposed by electrolysis and deposited in metallic form on the particles of mercury, by which it is at once amalgamated. Under the constant circular action and agitation of the stirrer the amalgam as formed descends to the bottom of the pan, where the mercury seizes upon any particles of coarse gold which may descend by gravitation to the bottom of the charge.
Though described with respect to chlorin and soluble reagents yielding chlorin, I am of opinion that my process should equally answer with bromin and soluble salts yielding bromin.
I am well aware that the various parts of my process, either singly or in certain co1n biuations, are well known, and wish it to be well understood that I do not claim as my invention any one of them singly or specifically or any two or more of them together in any combination whatever, except as the entire and particular combination indicated.
The black coating which gradually forms on the bottom of the pan around the mercurywell consists, mainly, of iron oxid, as proved by chemical tests. That it is practically a non-conductor of electricity is shown by the fact that the chlorin set free on the carbon shoes escapes as chlorin. This is proved by working the pan without any charge of ore in it and with only sufficient salt water in the pan to cover the carbon shoes. The gas then escapes at once and has been proved to be chlorin. If the black coating had been a good conductor of electricity, hydrogen would have been set free and, combining with the chlorin, would form hydrochloric acid. This is not found to be the case. Hence the black oxid is a non-conductor. As to the reaction whereby the black coating is formed, thciron of the pan is naturally an electropositive metal, while the carbon shoes are electronegative. If now while the dynamo is cut off from the pan a connection is made by a wire from the pan to the shoes and a galvanometer placed in circuit, a reverse current will at once be shown-i. e., the pan has become the anode and the shoes the cathode. Now in practice when a charge of ore has been treated and is being run out of the pan the current from the dynamo is cut off, because if allowed to pass through the pan when the charge gets low, the escape of chlorin becomes inconvenient to the workman, but as soon as the dynamo is cut oil the reverse action comes into play and the bottom of the pan becomes for a short time the anode. Then it is that the iron becomes oxidized. \Vhen the current from the dynamois turned on again, the pan at once becomes the cathode and the peroxid is reduced to a suboxid. B y degrees the coating gets thicker and the reaction less and less, until in about a week the coating has become suflicient to make the bottom of the pan practically a non-conductor.
Having now particularly described and ascertained the nature of my said invention and in what manner the same is to be performed, I declare that what I claim is 1. The herein-described process of treating ores consisting in introducing the ore into a pan adding thereto mercury and soluble salts capable of yielding chlorin by electrolysis raising the ore contents of the pan to about the boiling-point of water and passing a current of electricity through the heated mass while stirring the same to secure a simultaneous electrolytic chlorination and eleetro-amalgamation, and maintaining the anode out of vertical alinement with the mercury cathode substantially as described.
2. In combination, the pan having a concave bottom with a central Well, the furnace under the pan, the stirrer-shoes arranged to revolve about the central well leaving the same free means for revolving the shoes about the well and electrical connections to the shoes and pans, said shoes forming the anodes being out of vertical alinement with'the mercury in the central well forming the cathode substantially as described.
In witness whereof I have hereunto set my hand in presence of two witnesses.
J OSEPII HENRY IIAYCRAFT.
Witnesses:
FRANCIS II. SNOW, CHARLES S. Buaonss.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US579872A true US579872A (en) | 1897-03-30 |
Family
ID=2648551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US579872D Expired - Lifetime US579872A (en) | Ceaft |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US579872A (en) |
-
0
- US US579872D patent/US579872A/en not_active Expired - Lifetime
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