US815881A - Process for the reduction of ores. - Google Patents

Process for the reduction of ores. Download PDF

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Publication number
US815881A
US815881A US10258302A US1902102583A US815881A US 815881 A US815881 A US 815881A US 10258302 A US10258302 A US 10258302A US 1902102583 A US1902102583 A US 1902102583A US 815881 A US815881 A US 815881A
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ore
ores
lead
reduction
electrolyte
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US10258302A
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Clinton P Townsend
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ELMER A SPERRY
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ELMER A SPERRY
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B13/00Obtaining lead
    • C22B13/04Obtaining lead by wet processes

Definitions

  • Such impurities are not reduced by the hydrogen set free by the current, and therefore remain to contaminate the sponge, from which it is impracticable to separate them.
  • I have discovered that such ores may be reduced with great facility in a fused bath, preferably a bath consisting of the haloid salts of the alkali or alkaline-earth metals, and that by effecting the reduction under these conditions all of the objections above referred to are obviated.
  • The'lead is recovered not as a sponge, but as molten metal, which may be tapped continuously from the fusionvessel, the ore being fed continuously
  • molten metal which may be tapped continuously from the fusionvessel, the ore being fed continuously
  • the lead is drawn off through a'siphon or other tap-and fresh ore added continuously or from time to time.
  • the lead ore may be'pla'ced in a basket or perforated holder, which may be constructed of metal,
  • the cathode'connection being made, prefer ably, to the central portion of the body of the ore.
  • the ore is reduced, and the molten lead escapes through the perforations to the bottom of the fusion vessel, from which it may be removed in any suitable manner.
  • Tt' will be understood that the method is applicable to the reduction of all classes of ores and that the reduction of lead sulfid is taken as an'illustration merely.
  • the process possesses several important advantages, as follows: First, no oxygen be the decomposition of the electrolyte is correspondingly reduced. Third, a certain amount of sodium sulfid is thus formed which accumulates in; the bath until it is sufficient in quantity tocarry the current. Thereafter sodium sulfid' alone is decomposed, sulfur distilling orburning aroundthe anode, according as access of air is prevented orpermitted.
  • this sodium sulfid is decomposed at a lower electromotive force than the haloid salts, exerting a favorable influence on the process. Thereafter the electromotive force required is merely that necessary to overcome the ohmic resistance of the bath. Fifth, the electrolyte is inert toward galena in all stages of the process. Hence no metal exists in solution. This is important, since otherwise unavoidable losses of electrolyte would entail loss of metal.
  • the electrolyte should preferably be so chosen as to be inca able of acting chemically upon the ore or of issolving it to an appreciable extent.
  • I claim-- 1 The herein-described method of reducing sulfid ores, which consists in supporting the ore in a body of fused electrolyte which is substantially inert toward the-ore, and passing an electric current to said ore as cathode.
  • the herein-described method of reduci lead sulfid, wh ch consists in floatin the s fid upon abody of molten lead un er a fused electrolyte, connecting such sulfid as the cathode, and passing an electric current through the bath.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)

Description

v UNITED STATES ATENT OFFICE.
CLINTON P. TOWNSEND, OF WASHINGTON, DISTRIOT OF COLUMBIA, ASSIGNO'R TO ELMER A. SPERRY, OF BROOKLYN, NEW YORK.
Application filed April 12, 1962' Serial No. 102,583.
To all whom it may concern:
Be it known that I, CLINTON P. TOWNSEND, a citizen of the United States, residing at Washington, District ofColumbia, have inhas been electrolytically reduced by constior at intervals thereto.
tuting it the cathode or by placing it in con tact with the cathode in an aqueous electrolyte, generally sulfuric acid, and passing an electric current through the bath for long per riods, .amounting'usually to several days for a single charge. In this manner a sponge of lead is produced. This method has'several defects. It .is very slow, and it is difficult to make the reduction complete. The lead sponge recovered is not in available form for many purposes, and" the presence of'impuri ties in the ore is. very troublesome. Such impurities, of which zinc-blende may be taken as a type, are not reduced by the hydrogen set free by the current, and therefore remain to contaminate the sponge, from which it is impracticable to separate them. I have discovered that such ores may be reduced with great facility in a fused bath, preferably a bath consisting of the haloid salts of the alkali or alkaline-earth metals, and that by effecting the reduction under these conditions all of the objections above referred to are obviated. The'lead is recovered not as a sponge, but as molten metal, which may be tapped continuously from the fusionvessel, the ore being fed continuously By reason of the great difference in the specific gravities of the molten lead, the ore, and the electrolyte the ore floats upon the surface of the lead beneath the electrolyte and remains, therefore,
in the field of most active reduction until it is itself reduced, and any irreducible impurities which may be present in the ore collect above the lead and are removed in any suitable manner. A high-current density may be used, and the reduction proceeds, therefore, with great rapidity.
In operation the electrolyte is fused in a suitable vessel and the charge of galena added, a cathode connection being made to Specification of Letters Patent.
PROCESS FOR THE I REDUCTlON OF .ORES.
Patented March 20, 1906.
the charge, preferably by means of a pool'of lead upon which'it rests. Current of sultable character is passed from anodes, which may be of carbon or of metal, located in the molten' bath in proximity to the charge.
If it is desired to make the operation continuous, the lead is drawn off through a'siphon or other tap-and fresh ore added continuously or from time to time.
As an alternative construction the lead ore may be'pla'ced in a basket or perforated holder, which may be constructed of metal,
the cathode'connection being made, prefer ably, to the central portion of the body of the ore. Upon the passage of the current the ore is reduced, and the molten lead escapes through the perforations to the bottom of the fusion vessel, from which it may be removed in any suitable manner.
Tt'will be understood that the method is applicable to the reduction of all classes of ores and that the reduction of lead sulfid is taken as an'illustration merely. For the reduction of galena and other sulfid ores, however, the process possesses several important advantages, as follows: First, no oxygen be the decomposition of the electrolyte is correspondingly reduced. Third, a certain amount of sodium sulfid is thus formed which accumulates in; the bath until it is sufficient in quantity tocarry the current. Thereafter sodium sulfid' alone is decomposed, sulfur distilling orburning aroundthe anode, according as access of air is prevented orpermitted. Fourth, this sodium sulfid is decomposed at a lower electromotive force than the haloid salts, exerting a favorable influence on the process. Thereafter the electromotive force required is merely that necessary to overcome the ohmic resistance of the bath. Fifth, the electrolyte is inert toward galena in all stages of the process. Hence no metal exists in solution. This is important, since otherwise unavoidable losses of electrolyte would entail loss of metal.
In all cases the electrolyte should preferably be so chosen as to be inca able of acting chemically upon the ore or of issolving it to an appreciable extent.
While the invention contemplates, primarily, the reduction of ores which are conductive and themselves constitute the cathode, it is nevertheless applicable under proper conditions to non conducting ores, and certain claims which specifiy that the ore is floated upon a body of molten metal are intended to cover the reduction of both conductive and non-conductive ores.
The term ore is herein employed in its technical sense to cover concentrates, mattes, and other sources of metal which are applicable to the purposes of this invention.
I claim-- 1. The herein-described method of reducing sulfid ores, which consists in supporting the ore in a body of fused electrolyte which is substantially inert toward the-ore, and passing an electric current to said ore as cathode.
2. The herein-described method of reducing galena, which consists in supporting the ga ena in a body of fused electro yte which is substantially inert toward the galena, and
passing an electric current to said galena as cathode.
3. The herein-described method of reduc ing sulfid ores, which consists in sup orting the ore in a body of fused haloid sa t, and passing an electric current to said ore as catho e.
4. The herein-described method of reducin galena, which consists in supporting the ga ena in a body of fused haloid salt, and passing an electric current to said galena as cathode.
5. The herein-described method for the reduction of ores, which consists infloating the ore upon a body of molten metal under a fused electrolyte and reducing the ore by the passage of a current.
6. The herein-described method for the reduction of ores, which consists in floating the ore upon a body of molten metal, under a fused electrolyte, connecting such ore as the cathode, and reducing the ore by the passage of a current.
7. The herein-described method for the reduction of ores, which consists in floating the ore upon a body of the metal which forms the base of the ore, under a fused electrolyte, and
reducing it by the passage of a current.
8. The herein-described method for the reduction of ores, which consists in floating the ore upon a body of the metal which forms the base of the ore, under a fused electrolyte, connecting such ore as the cathode, and reducing it by the passage of a current.
9. The hereindescribed process of reducing lead ores, which consists in floatin the ore upon a body of molten metal, un er a fused electrolyte, connecting such ore as the cathode, and passing an electric current through the bath.
10. The herein-described method of reducing ores, which consists in floating the ore upon a body of molten lead under a fused electrolyte, and reducing such ore by the passage of an electric current.
11. The herein-described method of reducing ore, which consists in floating the ore upon a body of molten lead, under a fused electrolyte, connecting such ore as the cathode, and passing an electric current through the bath.
12. The herein-described method of reduci lead sulfid, wh ch consists in floatin the s fid upon abody of molten lead un er a fused electrolyte, connecting such sulfid as the cathode, and passing an electric current through the bath.
13. The herein-described method of reducing ores, which consists in floating the ore upon a. body of molten metal, under a fused electrolyte,- and reducing the ore by passing a current through the bath from superposed anodes.
14. The process of decomposing lead sulfid which consists in electrolytically se arating lead therefrom by bringing said s (1 into contact with a'cathode, in a fused electrolyte in which lead sulfid is substantially insoluble.
15. The process of decomposing lead sulfid which consists in electrolytically se arating lead therefrom by bringing said su fid into contact with a cathode, in a fused electrolyte, mainly of sodium chlorid.
In testimony whereof I affix my signature in presence of two witnesses.
CLINTON P. TOWNSEND;
Witnesses:
EUGENE A. BYRNES, CLAUDE I. PARKER.
US10258302A 1902-04-12 1902-04-12 Process for the reduction of ores. Expired - Lifetime US815881A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3954938A (en) * 1973-02-21 1976-05-04 Institute Of Gas Technology Removal of hydrogen sulfide from reducing gases

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3954938A (en) * 1973-02-21 1976-05-04 Institute Of Gas Technology Removal of hydrogen sulfide from reducing gases

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