US591141A - Process of and apparatus for electrolytic extraction of metals from their solutions - Google Patents
Process of and apparatus for electrolytic extraction of metals from their solutions Download PDFInfo
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- US591141A US591141A US591141DA US591141A US 591141 A US591141 A US 591141A US 591141D A US591141D A US 591141DA US 591141 A US591141 A US 591141A
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- 229910052751 metal Inorganic materials 0.000 title description 24
- 239000002184 metal Substances 0.000 title description 24
- 238000000034 method Methods 0.000 title description 21
- 150000002739 metals Chemical class 0.000 title description 12
- 238000000605 extraction Methods 0.000 title description 2
- 229910000497 Amalgam Inorganic materials 0.000 description 46
- 239000000243 solution Substances 0.000 description 37
- 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 11
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 11
- 239000010931 gold Substances 0.000 description 11
- 229910052737 gold Inorganic materials 0.000 description 11
- 239000011734 sodium Substances 0.000 description 11
- 229910052708 sodium Inorganic materials 0.000 description 10
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 9
- 229910052753 mercury Inorganic materials 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 238000005868 electrolysis reaction Methods 0.000 description 6
- 238000005192 partition Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 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 2
- 230000002706 hydrostatic effect Effects 0.000 description 2
- 239000011244 liquid electrolyte Substances 0.000 description 2
- 229910001023 sodium amalgam Inorganic materials 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910000567 Amalgam (chemistry) Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- MJGFBOZCAJSGQW-UHFFFAOYSA-N mercury sodium Chemical compound [Na].[Hg] MJGFBOZCAJSGQW-UHFFFAOYSA-N 0.000 description 1
- 238000010310 metallurgical process Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/23—Oxidation
Definitions
- My invention relates to those metallurgical processes in which a metal is recovered from Isolution by means of electrolysis, and the Imain feature of my improvement lies in the composition, preparation, disposal, and treat" finent of the positive pole or anode which is I to be employed in conducting the electrolysis. Briefly stated, it consists in employing as the anode an amalgam of such composition that the attack of the electrolyte shall be'substantially limited to the non-mercurial ingredient of such physical character as to be substantially liquid and so disposed as to permit the renewal of the anode as the consumption thereof occurs.
- the mercury acts as a vehicle for the continual supply of the electropositive ingredient to the attack of the elec- I contemplate the use of a great va- I POIJZtSSIUm, aluminium, zinc, or ammonia, the proportion of mercury being always, however,
- the cathode or receiv ing plate upon which the metal in solution is to be deposited When convenient, this plate may be formed of the same metal as that which is to be deposited. If this is not convenient, any other substance which is capable of receiving the metal as it is deposited and from which it can be removed will answer the purpose.
- the anode In order to practice my invention, however, it is necessary that the anode should consist of a combination of mercury and one or more of the metals (or ammonia) with which mercury is capable of forming an amalgam. It is, furthermore,
- the proportion of mercury shall be sufficient-ly great to preserve the mobility of the amalgam.
- the nature of the metal in the amalgam may vary as the character of the solution from which the metal is to be extracted or the convenience of the operation may dictate.
- Figures 1 and 2 are cross-sections of such apparatus, while Fig. 3 is a longitudinal sec tion of either apparatus when fitted with means for obtaining constant motion of the 1 Fig. 2 differs from Fig. 1 in I that it shows combined with the electrolytic cathode-plates.
- A represents the tank, which be of any convenient size and shape.
- cyanid plates are constituted cathodes and the amalgain an anode.
- a porous plate or diaphragm e is interposed between these electrodes, dividing the tank horizontally into two compartments.
- the lower compartment is filled from the surface of the amalgam to the plate with any suitable electrolyteas, for exam- ;ple, a simple solution of cyanid of sodium.
- the rate of flow of the cyanid solution should depend upon the rapidity of the electrolysis, due precaution being taken to keep either the solution or the cathode-plates in constant motion, so as to minimize deleterious second- I 5 ary reactions and insure full efficiency of deposition by the current passing.
- the plates 0 are supported by means of a horizontal frame L, which rests upon the sides of the tank A. Said frame is connected by means of a pitman m with an eccentric M, whose shaft is provided with a driving-pulley N, actuated by means of a belt 72. By the rotation of the eccentric M at any desired speed a reciprocating movement of the entire sys- 3 5 tem of the cathode-plates c is effected.
- liquid-amalgam anode For the greater protection of the amalgam, which is exposed in the external passage-way, its surface may be covered by a layer of naphtha.
- the liquid-amalgam anode may thus be maintained at any'desired level and its mercurial ingredient may be drawn off, the two operations being entirely independent of one another.
- the advantage of the interposed diaphragm is that the gold solution and the amalgam do not come in physical contact, thus preventing the possibility of any chemical action between them. There is also the further advantage that any gold which may fall off the receiving-plate will be caught by the diaphragm instead of falling into the amalgam.
- amalgam gives up its nonmercurial ingredient to draw off the mercury by means of the spigot (Z and replace it by fresh amalgam, which amalgam may be manufactured by means of any well-known process.
- FIG. 2 An alternative form of apparatus is illustrated in Fig. 2, by means of which the continuous formation of amalgam may be eifected electrolytically by the same current which effects the electrolytic deposition of the gold.
- the right-hand portion corresponds in all details to the apparatus which is shown in Fig. 1, I) representing the amalgam at the bottom of the tank, 6 the diaphragm, and c the suspended cathodes.
- hydrostatic pressure may be obtained by the stand-pipe f.
- a second electrolytic cell is provided, which cell occupies the left-hand portion of the drawings,communicating at the bottom with the right-hand portion in precisely the same manner as does the external passage-way shown in Fig. 1.
- This left-hand compartment 9 has a covered top. It is filled with a suitable electrolyte, as hereinafter explained, within which is suspended a positive electrode II, say, of carbon. The bottom of this compartment is also filled with amalgam and means are to be assumed for maintaining its free circulation from one compartment to the other beneath the partition, but as. such means are well known they are not shown.
- the compartment 9 is kept filled (by means of the intake and outlet openings j k) with a strong solution of chlorid of sodium.
- the course of the current is from the positive electrode II through the brine to the amalgam, and thence under the partition through the cyanid solution, the diaphragm, and the gold solution to the negative receiving-plate 0.
- the chlorid of sodium is decomposed, the chlorin being released and collected through the discharge-tube m, (whence it may be employed as a useful by-product,) while the sodium enters into the amalgam, continually renewing that which is lost by reason of the action of the cathode, which has been explained.
- the electrolytic action in the right-hand compartthus continuous, simultaneous, and correlative to each other.
- the anode being in a liquid form it is capable of being continuously renewed, (by means of the simple apparatus which I have described) from which it results that all of the disadvantages ordinarily incident to solid but soluble anodes are obviated.
- the anode whatever be its constitution, is more or less rap-- idly destroyed and must be replaced.
- Such ireplacement requires time and trouble and ITO Both processes are causes an interruption of the continuity of the process.
- the salt from which the amalgam is to be formed. can frequently be chosen so that its other ingredients are of immediate value.
- the by-product resulting from the decomposition of the chlorid of sodium, which results in the formation of sodium amalgam is chlorin gas, which in very many gold processes is of the highest utility in the treatment by chlorination. of certain portions of the gold ore which are not amenable to the cyanid process.
- My invention is based upon the peculiar availability of a liquid amalgam as an anode under specified conditions and in a specific process forwhich it has a peculiar and definite value, and in which I believe myself to be the first to so organize its employment as to render it commercially practicable.
- I claim- 1 The process of extracting metals from their solutions, which consists in subjecting such solutions to the electrolytic action of an electric current passing into the solution by a liquid-amalgam anode, and separating said anode from its cathode bya porous partition, substantially as described.
- An apparatus for electrolytically separating metals from their solutions which consists in the combination of a cell with means for electrolytically producing an amalgam therein; a second cell to which the amalgam formed in the first cell is conveyed; a cathode in said second cell as to which the amalgam therein is constituted an anode; a porous partition between said anode and cathode; means for passing the metal-containing solution through the cathode-compartment thus formed; and means for subjecting the liquid in the anode-compartment to a pressure greater than that existingin the cathode-compartment, substantially as described.
- An apparatus for electrolytically separating metals from their solutions which consists in the combination, with a tank containing a liquid-amalgam anode in its bottom region, and an electrolyte in the region above said anode, and having a cathode-plate arranged in the region of the electrolyte; of a porous partition arranged above said anode and dividing the region of the electroyte horizontally into two compartments; and means, substantially as set forth, (as a stand-pipe,) communicating with the lower of said two compartments, whereby a body of liquid electrolyte maybe maintained in said lowercompartment at a pressure in excess of the pressure of the body of liquid electrolyte in the upper compartment,substantially as and for the purposes specified.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Metals (AREA)
Description
(No Model.)
J. W. RICHARDS.
PROCESC OI AND APPARATUS FOR ELECTROLYTIC EXTRACTION OI METALS FROM THEIR SOLUTIONS.
No. 591,141. Patented 001. 5,1897.
WITNESSES: 4 I INVENTOR:
WAR;
Ma mums Perms co. wow-1mm WASHINGTON. nfc
TJ'NTTED STATES PATENT OFFICE.
JOSEPH W. RICHARDS, OF BETHLEHEM, PENNSYLVANIA.
PROCESS OF AND APPARATUS FOR ELECTROLYTIC EXTRACTION F METALS FROM THEIR SOLUTIONS.
SPECIFICATION forming part of Letters Patent No. 591,141, dated October 5, 1897. Application filed March 6, 1897. 1 Serial No. 626,305. (No model.)
To aZZ whom it may concern.-
Be it known that I, JOSEPH W'. RICHARDS, a subject of the Queen of Great Britain, residing at Bethlehem, in the State of Pennsylvania, have invented certain new and useful Improvements in Processes of and Apparatus for the Electrolytic Extraction of Metals from Their Solutions, of which the. following is a specification, reference being had to the accompanying drawings.
My invention relates to those metallurgical processes in which a metal is recovered from Isolution by means of electrolysis, and the Imain feature of my improvement lies in the composition, preparation, disposal, and treat" finent of the positive pole or anode which is I to be employed in conducting the electrolysis. Briefly stated, it consists in employing as the anode an amalgam of such composition that the attack of the electrolyte shall be'substantially limited to the non-mercurial ingredient of such physical character as to be substantially liquid and so disposed as to permit the renewal of the anode as the consumption thereof occurs. In this composition and disposal of the anode the mercury acts as a vehicle for the continual supply of the electropositive ingredient to the attack of the elec- I contemplate the use of a great va- I POIJZtSSIUm, aluminium, zinc, or ammonia, the proportion of mercury being always, however,
,f kept sufficiently great to preserve the fluidity of the compound.
For the purposes of my invention it is immaterial what may be the source of the electric current by means of which the electrolysis is conducted. It is also immaterial what may be the nature of the cathode or receiv ing plate upon which the metal in solution is to be deposited. When convenient, this plate may be formed of the same metal as that which is to be deposited. If this is not convenient, any other substance which is capable of receiving the metal as it is deposited and from which it can be removed will answer the purpose. In order to practice my invention, however, it is necessary that the anode should consist of a combination of mercury and one or more of the metals (or ammonia) with which mercury is capable of forming an amalgam. It is, furthermore,
necessary that the proportion of mercury shall be sufficient-ly great to preserve the mobility of the amalgam. Within these limits the nature of the metal in the amalgam may vary as the character of the solution from which the metal is to be extracted or the convenience of the operation may dictate.
For the purpose of explaining a convenient method of practicing my invention I have shown in the accompanying drawings alternative forms of suitable apparatus.
Figures 1 and 2 are cross-sections of such apparatus, while Fig. 3 is a longitudinal sec tion of either apparatus when fitted with means for obtaining constant motion of the 1 Fig. 2 differs from Fig. 1 in I that it shows combined with the electrolytic cathode-plates.
tank a receptacle and apparatus by means of which the same current which conducts the electrolysis of the metal-containing solution may also be rendered effective for the purpose of producing continuously and elec- In Fig. 1, A represents the tank, which be of any convenient size and shape. One
of the sides a of the tank fails bya short distance of reaching the bottom of the tank, the
bottom being extended and turned up beyond this side, so as to form an external supply I passage-way isolated from the main body of the tank. The entire bottom of the tank. is I filledwith a liquid amalgam bas, for instance, sodium amalgam-the height of the amalgam being well above the space left at the bottom of the side a. Above the amalgam is hung a series of receiving-plates c, which may either be of gold or of any sub stance capable of receiving a deposit of gold upon it and also of acting as an electrode. By means of electrical connections these.
plates are constituted cathodes and the amalgain an anode. A porous plate or diaphragm e is interposed between these electrodes, dividing the tank horizontally into two compartments. Through the upper of these com- 5 partments flows the cyanid solution carrying the gold. The lower compartment is filled from the surface of the amalgam to the plate with any suitable electrolyteas, for exam- ;ple, a simple solution of cyanid of sodium. Id The rate of flow of the cyanid solution should depend upon the rapidity of the electrolysis, due precaution being taken to keep either the solution or the cathode-plates in constant motion, so as to minimize deleterious second- I 5 ary reactions and insure full efficiency of deposition by the current passing. If the rate of flow of the solution through the tank is sufficiently great, this flow in itself supplies the requisite motion; otherwise motion of the cathode-plates may be resorted to, which motion may be obtained by mounting the entire series of plates upon a slowly-reciprocating frame, as shown in Fig. 3, where I have illustrated in transverse section an apparatus provided with convenient means for effecting this motion of the cathode-plates.
The plates 0 are supported by means of a horizontal frame L, which rests upon the sides of the tank A. Said frame is connected by means of a pitman m with an eccentric M, whose shaft is provided with a driving-pulley N, actuated by means of a belt 72. By the rotation of the eccentric M at any desired speed a reciprocating movement of the entire sys- 3 5 tem of the cathode-plates c is effected.
In order to prevent any passage of the goldcontaining solution through the porous diaphragm to the lower solution, a slight hydrostatic pressure may be maintained in the 4.0 lower solution by means of the stand-pipe f. i The action of the electrolytic current causes 3 the decomposition of the double cyanid salt, s the gold being deposited on the plate 0 and being replaced in the solution by a propor- 5 tionate quantity of sodium set free from the amalgam. As the process proceeds the amalgam, constantly loosing its sodium, is replaced by fresh amalgam supplied from an external source through the isolated passageway, that which is exhausted being drawn off by means of the spigot (1 upon the other side of the tank. For the greater protection of the amalgam, which is exposed in the external passage-way, its surface may be covered by a layer of naphtha. The liquid-amalgam anode may thus be maintained at any'desired level and its mercurial ingredient may be drawn off, the two operations being entirely independent of one another.
The advantage of the interposed diaphragm is that the gold solution and the amalgam do not come in physical contact, thus preventing the possibility of any chemical action between them. There is also the further advantage that any gold which may fall off the receiving-plate will be caught by the diaphragm instead of falling into the amalgam.
ment proceeds as before.
In the apparatus illustrated in Fig. 1 it is necessary as the amalgam gives up its nonmercurial ingredient to draw off the mercury by means of the spigot (Z and replace it by fresh amalgam, which amalgam may be manufactured by means of any well-known process.
An alternative form of apparatus is illustrated in Fig. 2, by means of which the continuous formation of amalgam may be eifected electrolytically by the same current which effects the electrolytic deposition of the gold. In this figure of the drawings the right-hand portion corresponds in all details to the apparatus which is shown in Fig. 1, I) representing the amalgam at the bottom of the tank, 6 the diaphragm, and c the suspended cathodes. As above, hydrostatic pressure may be obtained by the stand-pipe f. Instead, however, of the external passage-way for the supply of the amalgam a second electrolytic cell is provided, which cell occupies the left-hand portion of the drawings,communicating at the bottom with the right-hand portion in precisely the same manner as does the external passage-way shown in Fig. 1. This left-hand compartment 9 has a covered top. It is filled with a suitable electrolyte, as hereinafter explained, within which is suspended a positive electrode II, say, of carbon. The bottom of this compartment is also filled with amalgam and means are to be assumed for maintaining its free circulation from one compartment to the other beneath the partition, but as. such means are well known they are not shown.
Let it be supposed that the compartment 9 is kept filled (by means of the intake and outlet openings j k) with a strong solution of chlorid of sodium. The course of the current is from the positive electrode II through the brine to the amalgam, and thence under the partition through the cyanid solution, the diaphragm, and the gold solution to the negative receiving-plate 0. At the anode the chlorid of sodium is decomposed, the chlorin being released and collected through the discharge-tube m, (whence it may be employed as a useful by-product,) while the sodium enters into the amalgam, continually renewing that which is lost by reason of the action of the cathode, which has been explained. The electrolytic action in the right-hand compartthus continuous, simultaneous, and correlative to each other.
The following advantages of myinvention may be especially pointed out:
First. The anode being in a liquid form it is capable of being continuously renewed, (by means of the simple apparatus which I have described) from which it results that all of the disadvantages ordinarily incident to solid but soluble anodes are obviated. In the ordinary practice of the electrolytic deposition of metals from their solutions the anode, whatever be its constitution, is more or less rap-- idly destroyed and must be replaced. Such ireplacement requires time and trouble and ITO Both processes are causes an interruption of the continuity of the process.
, Second. Not only is the regeneration of the" anode continuous, but whatever be the salt used as a solvent to bring the metal into solution the use of mercury as a vehicle makes it possible to choose the amalgam so that it shall contain a metallic base of that salt, and
i in such case the salt-is regenerated by the electrolysis. Thus, as has been explained, for cyanid solutions, whether of sodium or of potassium,sodium or potassium amalgam may be employed. For a solution of zinc in an ammonium salt ammonium amalgam may be employed, &c., and it must be particularly emphasized that the metals which most commonly form the base of those salts which are employed in metallurgical-solution processes are the alkaline and earthy metals'and those allied to them, which metals, by reason of their nature, it-is either impossible or very difficult to employ as anodes in any other instances be cheaply prepared from its cheapest salt, thus costing far less than if it were bought or prepared and used in its metallic state without being in an amalgam.
Fourth. The salt from which the amalgam is to be formed. can frequently be chosen so that its other ingredients are of immediate value. Thus in the process which has been outlined as an example the by-product resulting from the decomposition of the chlorid of sodium, which results in the formation of sodium amalgam, is chlorin gas, which in very many gold processes is of the highest utility in the treatment by chlorination. of certain portions of the gold ore which are not amenable to the cyanid process.
Fifth. The process lends itself readily to such a combination as has been outlined in connection with the description of Fig. 2, by which the amalgam-producing apparatus is combinedwitlr'the apparatus for the decomposition of the metal-carrying solution, so as to render it possible to employ not only the same source of electricity but the same elec- .tric circuit to do both the work of producing electrolytically the amalgam and of effecting the electrolytic decomposition of the metalcarrying solution.
I desire it to be distinctly borne in mind that in my process neither the amalgam nor either of its constituents has any independent chemical action upon the solution apart from that which is incident to the electrolytic action.
I am aware that it has hitherto been proposed to use an amalgam-as, for example, sodium amalgamfor the purpose of chemically decomposing gold solutions. Such processes have nothing in common with my process, not only by reason of the fact that in my process the decomposition of the solution is electrolytic rather than chemical, but because the practical result of the chemical precipitation is inevitably the combination of the mercury with the metal which it is desired to obtain, resulting in the formation of a second amalgam, while in my process the metal to be obtained cannot possibly associate itself with the amalgam, but is driven away from it and deposited upon the receiving surface which is constituted the cathode.
I am also aware that it is not new, broadly speaking, to employ a body of mercury in such relation to an electric circuit as that it shall actas an anode, and I do not broadly claim the same.
My invention is based upon the peculiar availability of a liquid amalgam as an anode under specified conditions and in a specific process forwhich it has a peculiar and definite value, and in which I believe myself to be the first to so organize its employment as to render it commercially practicable.
In using the word liquid in this specification and in the following claims to designate the physical condition of the anode, I do not desire to limit myself to an amalgam which is liquid in the more restricted sense, but mean to comprehend thereunder any amalgam which has a mobility approximating that of aliquid, even though it be somewhat viscous or pasty.
Having thus described my invention, I claim- 1. The process of extracting metals from their solutions, which consists in subjecting such solutions to the electrolytic action of an electric current passing into the solution by a liquid-amalgam anode, and separating said anode from its cathode bya porous partition, substantially as described.
2. The process of extracting metals from their solutions, which consists in subjecting such solutions to the electrolytic action of a pair of electrodes, of which the anode is composed of a liquid amalgam, with a porous plate interposed between the electrodes, the solution from which the metal is to be extracted passing through the cathode-compartment, substantially as described.
3. The process of extracting metals from their solutions, which consists in subjecting them to electrolytic action by means of a liquid-amalgam anode situated in one of two 4 ten-141 formed in the first cell is conveyed; a cathode in said second cell as to which the amalgam therein is constituted an anode; a porous means substantially as set forth by which the amalgam formed in the first cell is conveyed to the second cell; a cathode in said second cell, as to which the amalgam therein is constituted an anode; a porous partition between said anode and cathode; and electrical con nections whereby said first and second cells are maintained in series in the same electric circuit, substantially as described.
6. An apparatus for electrolytically separating metals from their solutions, which consists in the combination of a cell with means for electrolytically producing an amalgam therein; a second cell to which the amalgam formed in the first cell is conveyed; a cathode in said second cell as to which the amalgam therein is constituted an anode; a porous partition between said anode and cathode; means for passing the metal-containing solution through the cathode-compartment thus formed; and means for subjecting the liquid in the anode-compartment to a pressure greater than that existingin the cathode-compartment, substantially as described.
7. An apparatus for electrolytically separating metals from their solutions, which consists in the combination, with a tank containing a liquid-amalgam anode in its bottom region, and an electrolyte in the region above said anode, and having a cathode-plate arranged in the region of the electrolyte; of a porous partition arranged above said anode and dividing the region of the electroyte horizontally into two compartments; and means, substantially as set forth, (as a stand-pipe,) communicating with the lower of said two compartments, whereby a body of liquid electrolyte maybe maintained in said lowercompartment at a pressure in excess of the pressure of the body of liquid electrolyte in the upper compartment,substantially as and for the purposes specified.
J O-SEPII W. RICHARDS.
Witnesses:
R. W. LEIBERT, ADELE S. LEIBERT.
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| Publication Number | Publication Date |
|---|---|
| US591141A true US591141A (en) | 1897-10-05 |
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| US591141D Expired - Lifetime US591141A (en) | Process of and apparatus for electrolytic extraction of metals from their solutions |
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