US752320A - Jose baxeees de alzugaray - Google Patents
Jose baxeees de alzugaray Download PDFInfo
- Publication number
- US752320A US752320A US752320DA US752320A US 752320 A US752320 A US 752320A US 752320D A US752320D A US 752320DA US 752320 A US752320 A US 752320A
- Authority
- US
- United States
- Prior art keywords
- solution
- ore
- chlorid
- zinc
- copper
- 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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- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 44
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 38
- 229910052802 copper Inorganic materials 0.000 description 38
- 239000010949 copper Substances 0.000 description 38
- 239000011133 lead Substances 0.000 description 34
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 34
- 229910052725 zinc Inorganic materials 0.000 description 34
- 239000011701 zinc Substances 0.000 description 34
- 229910052751 metal Inorganic materials 0.000 description 32
- 239000002184 metal Substances 0.000 description 32
- 238000002386 leaching Methods 0.000 description 28
- 150000002739 metals Chemical class 0.000 description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 229910052709 silver Inorganic materials 0.000 description 14
- 239000004332 silver Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 238000001354 calcination Methods 0.000 description 10
- WGSLWEXCQQBACX-UHFFFAOYSA-N Chlorin Chemical compound C=1C(C=C2)=NC2=CC(C=C2)=NC2=CC(C=C2)=NC2=CC2=NC=1CC2 WGSLWEXCQQBACX-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 239000003513 alkali Substances 0.000 description 8
- 229910052742 iron Inorganic materials 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 4
- LQCOCUQCZYAYQK-UHFFFAOYSA-N (2-aminophenyl)arsonic acid Chemical compound NC1=CC=CC=C1[As](O)(O)=O LQCOCUQCZYAYQK-UHFFFAOYSA-N 0.000 description 2
- 229960005069 Calcium Drugs 0.000 description 2
- 108010077798 Calcium Proteins 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- XCAUINMIESBTBL-UHFFFAOYSA-N Lead(II) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 2
- 235000015450 Tilia cordata Nutrition 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 235000001465 calcium Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- -1 chlorids or sulfates Chemical class 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 229910052803 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- MBMLMWLHJBBADN-UHFFFAOYSA-N iron-sulfur Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 2
- 229910052981 lead sulfide Inorganic materials 0.000 description 2
- 229940056932 lead sulfide Drugs 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative Effects 0.000 description 2
- 230000002035 prolonged Effects 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- C22B11/04—Obtaining noble metals by wet processes
Definitions
- the object of this invention is to treat what are known as complex ores or other metal containing compounds for the purpose of extracting, as the case may be, cobalt, copper, lead, nickel, silver, zinc, and other heavy metals therefrom, and an essential feature of the invention consists in leaching the crushed ores with an acidulated solution of a chlorid of an alkali or alkali-earth metal and of a calcination or roasting of the metals contained in the complex ore being extracted by means of this invention successively or, selectively,
- the materials which have been found useful in solution are chlorid of sodium, cal cium, or magnesium and proto and per chlorid of iron acidulated with a suitable acid.
- An acid which has been found exceedingly satisfactory in this connection is hydrochloric acid; but other acids or mixtures thereof which will yield free chlorin may also be employed.
- chlorid of manganese formed by dissolving peroxid of manganese in hydrochloric acid.
- the copper will have been extracted and by continuing the treatment for from five to seven days a total percentage .of from eighty-six as ninety-four per centcan be obtained.
- Lead sulfid being less oxidizable, only some thirty percent. of lead will be extracted during this stage of the process; but from the Zinc sulfid, upon which the oxidizing mixture has little effect, only about 1.14 percent. of the zinc will be obtained at this stage. It will thus be seen that after this first stage of the treatment practically all the copper con-' tents are recovered; but it will be necessary to proceed further to extract the remaining lead and zinc. To this end the residual ore is well washed and dried, and it is then roasted at a low temperature.
- the action of the strongly-oxidizing acidulated chlorid solution on the crushed ore is such that the ore becomes partially disintegrated or rendered porous by the leaching operation, and therefore the roasting operation canbe carried out at a relatively low temperature.
- the roasting operation is thus rendered much easier than under ordinary circumstances. In fact, about twenty-five per cent. of the sulfur contents are volatilized at a temperature ranging from 165 to 200 cent-igrade.
- the roasted ore will consist of amixture of oxids, chiefly of zinc and lead, from which these metals can be extracted in the form of suitable salts, such as chlorids or sulfates, by a second leaching with a weak solution having a character consonant with the nature of the salt to be produced.
- suitable salts such as chlorids or sulfates
- the metals may be obtained as chlorids by leaching for afew hours with a Weaker acidulated solution of the chlorids above mentioned, which converts the zinc into a soluble chlorid. From this solution the zinc may be precipitated with a suitable alkali earthy oxid, such as lime or magnesia.
- the zinc thus obtained will be distilled in the usual way for metal.
- the lead will precipitate as chlorid.
- the copper obtained during the first stage of the operation may be separated by means of iron, the silver, if there is any, by means of copper, and such lead as has been dissolved will separate as a crystallized chlorid.
- the acids may be added to the chlorid solution in the liquid state in suitable proportions or may be blown through the mixture of ore and chlorid solution in the gaseous state.
- sulfuric acid will be used for the leaching solution at the later stage after the calcination. In this case the lead will remain as an insoluble precipitate of sulfate and separate in this form.
- the solutions may be electrolyzed and the metals deposited at the cathode, as is well understood.
- the ore subjected to treatment according to this invention may be treated in lump (which, however, requires a longer period of. treatment) or in any degree of fineness; but it has been found on the average that thirty mesh answers the best.
- the leaching solutions at the several stages of the treatment may be warmed to a suitable degree. This will render the operation more rapid.
- What I claim as my invention is 1.
- the process of extracting the said metals selectively which consists in leaching the ore with a solution composed of a mixture of a chlorid of an alkali or earth-alkali metal with a chlorid of a metal other than those of the alkali or earth-alkali series and an acid before calcination or roasting whereby the copper is obtained in solution, then washing and drying the ore, roastingthe partially-disintegrated ore at a low temperature, extracting the metals from the roasted ore in form ofsalts by means of a second and weaker leaching solution having a character consonant with the nature of the salt it is desired to obtain, and recovering the metals in the usual way as herein described.
Description
U NITED STATES Patented February 16, 1904.
PATENT OFFICE.
ExTRAoTloN'oF' METALS FR M COMPLEX ones.
SPECIFICATION forming part of Letters Patent RIO. "752,320, dated February 16, 1904.
Application filed July 14,1903. Serial No. 165,501. (No specimens.)
To all whom it may concern: 7 Be it known that 1, Jose BAXERES DE ALzU- GARAY, a citizen of Argentina, and a resident of Lola Villa, Bromley, in the county of Kent, England, have invented certain new and useful Improvements in or Relating to the Extraction of Metals from Complex Ores, of which the following is a specification. a
The object of this invention is to treat what are known as complex ores or other metal containing compounds for the purpose of extracting, as the case may be, cobalt, copper, lead, nickel, silver, zinc, and other heavy metals therefrom, and an essential feature of the invention consists in leaching the crushed ores with an acidulated solution of a chlorid of an alkali or alkali-earth metal and of a calcination or roasting of the metals contained in the complex ore being extracted by means of this invention successively or, selectively,
as will be hereinafter more particularly explained. The materials which have been found useful in solution are chlorid of sodium, cal cium, or magnesium and proto and per chlorid of iron acidulated with a suitable acid. An acid which has been found exceedingly satisfactory in this connection is hydrochloric acid; but other acids or mixtures thereof which will yield free chlorin may also be employed, To the acidulated chlorid solution may be added, if desired, chlorid of manganese, formed by dissolving peroxid of manganese in hydrochloric acid. v v
In working this invention it has been found that complex sulfid ores are attacked and decomposed by the above-described mixture of acidulated chlorids in,.the following order: first, the sulfids of copper and silver; second, the sulfid of lead, and, third, the sulfid of zinc, while iron sulfid, if there is any, remains practically undecomposed even after prolonged treatment by the leaching solution. The mechanism of this reaction is that free chlorin is generated most probably by the dissociation of unstable intermediate chlorin compoundsformed in the mixture, which free chlorin in the presence of the water acts as a powerful oxidizer.
For the purpose of testing the efiicacy of the process which forms the subject of the present invention ores of an extremely intractable character have been experimented upon-such, for instance, as an ore containing on an average: zinc, 21.64 per cent; lead, 19.37 per cent; copper, 6.48 per cent; iron,
5.39 per cent; sulfur, 20.28 per cent; but
the invention is not confined to treating such an ore. I r
; In carrying out the invention as applied to the treatment of ore represented by the above analysis the crushed ore is treated with an equal weight of the acidulated chlorid solution without previous calcination. ()n account of the Well-known ready oxidizability of'copper sulfid it will be found that after some five hours treatment about fifty per cent. of
the copper will have been extracted and by continuing the treatment for from five to seven days a total percentage .of from eighty-six as ninety-four per centcan be obtained. Lead sulfid being less oxidizable, only some thirty percent. of lead will be extracted during this stage of the process; but from the Zinc sulfid, upon which the oxidizing mixture has little effect, only about 1.14 percent. of the zinc will be obtained at this stage. It will thus be seen that after this first stage of the treatment practically all the copper con-' tents are recovered; but it will be necessary to proceed further to extract the remaining lead and zinc. To this end the residual ore is well washed and dried, and it is then roasted at a low temperature. The action of the strongly-oxidizing acidulated chlorid solution on the crushed ore is such that the ore becomes partially disintegrated or rendered porous by the leaching operation, and therefore the roasting operation canbe carried out at a relatively low temperature. The roasting operation is thus rendered much easier than under ordinary circumstances. In fact, about twenty-five per cent. of the sulfur contents are volatilized at a temperature ranging from 165 to 200 cent-igrade. The roasting of the ore containing the zinc and lead sulfide, otherwise a lengthy and difficult operation, after the treatment with the acidulated chlorid solution takes place with great rapidity and is V I V as easy as the roasting of arsenical pyrites and even easier. Y
The roasted ore will consist of amixture of oxids, chiefly of zinc and lead, from which these metals can be extracted in the form of suitable salts, such as chlorids or sulfates, by a second leaching with a weak solution having a character consonant with the nature of the salt to be produced. The metals may be obtained as chlorids by leaching for afew hours with a Weaker acidulated solution of the chlorids above mentioned, which converts the zinc into a soluble chlorid. From this solution the zinc may be precipitated with a suitable alkali earthy oxid, such as lime or magnesia. The zinc thus obtained will be distilled in the usual way for metal. The lead will precipitate as chlorid.
The copper obtained during the first stage of the operation may be separated by means of iron, the silver, if there is any, by means of copper, and such lead as has been dissolved will separate as a crystallized chlorid.
The acids may be added to the chlorid solution in the liquid state in suitable proportions or may be blown through the mixture of ore and chlorid solution in the gaseous state.
If sulfates are the salts desired, sulfuric acid will be used for the leaching solution at the later stage after the calcination. In this case the lead will remain as an insoluble precipitate of sulfate and separate in this form.
Instead of separating the metals in solution byother metals or reagents the solutions may be electrolyzed and the metals deposited at the cathode, as is well understood.
The ore subjected to treatment according to this invention may be treated in lump (which, however, requires a longer period of. treatment) or in any degree of fineness; but it has been found on the average that thirty mesh answers the best. The leaching solutions at the several stages of the treatment may be warmed to a suitable degree. This will render the operation more rapid.
What I claim as my invention is 1. In the treatment of complex ores, such for instance, as contain copper, lead, silver and zinc in comparatively large quantities, the process of extracting the said metals selectively which consists in leaching the ore with a solution composed of a mixture of a chlorid of an alkali or earth-alkali metal with a chlorid of a metal other than those of the alkali or earth-alkali series and an acid before calcination or roasting whereby the copper is obtained in solution, then washing and drying the ore, roastingthe partially-disintegrated ore at a low temperature, extracting the metals from the roasted ore in form ofsalts by means of a second and weaker leaching solution having a character consonant with the nature of the salt it is desired to obtain, and recovering the metals in the usual way as herein described.
2. In the treatment of complex ores, such for instance as contain copper, lead, silver and zinc in comparatively large quantities, the process of extracting the said metals selectively which consists in leaching the ore with an acidulated chlorid solution, before roasting or calcination whereby the copper is obtained in solution, then washing and drying the ore, roasting the partially-disintegrated ore at a low temperature, and finally leaching the roasted ore with a weaker acidulated chlorid solution, whereby the zinc is obtained in solution, while the lead precipitates, and recovering from the solutions the copper with iron and the zinc with an earthy or alkali-earthy oxid, as herein described, and the silver by meansof copper or of any suitable metal or reagent.
3. The process for extracting copper from complex ores containing copper, lead, silver and zinc in comparatively large quantities, which consists in leaching the crushed ore with a solution composed of a mixture of an alkaline chlorid, a metallic chlorid and an acid without calcination-or roasting, and drawing oif the solution and separating the copper in any well-known manner as herein described.
4. The process for extracting zinc and lead from complex ores containing copper, lead'and zinc in comparatively large quantities, which consists in first leaching the ore in an acidulated chlorid solution whereby it is partially disintegrated and the copper is obtained therefrom in solution, then washing, drying and roasting the so partially-disintegrated ore, and finally leaching the roasted ore in a weak acidulated chlorid solution, whereby the lead precipitates as a chlorid, and the zinc enters into solution and is precipitated by means of an alkali-earthy oxid and is finally recovered by distillation in the usual way, all as herein de scribed.
In testimony whereof Ihave signed my name to this specification in the presence of two subscribing witnesses.
JOSE BAXERES DE ALZUGARAY.
Witnesses:
ALFRED S. BISHOP, W. M. HARRIS.
Publications (1)
Publication Number | Publication Date |
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US752320A true US752320A (en) | 1904-02-16 |
Family
ID=2820813
Family Applications (1)
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US752320D Expired - Lifetime US752320A (en) | Jose baxeees de alzugaray |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3896208A (en) * | 1972-06-26 | 1975-07-22 | Ethyl Corp | HCl Treatment of copper sulfide minerals |
US4288304A (en) * | 1975-04-21 | 1981-09-08 | Societe Miniere Et Metallurgique De Penarroya | Hydrometallurgical process for treatment of sulphur ores |
US20050118081A1 (en) * | 2003-09-30 | 2005-06-02 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
-
0
- US US752320D patent/US752320A/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3896208A (en) * | 1972-06-26 | 1975-07-22 | Ethyl Corp | HCl Treatment of copper sulfide minerals |
US4288304A (en) * | 1975-04-21 | 1981-09-08 | Societe Miniere Et Metallurgique De Penarroya | Hydrometallurgical process for treatment of sulphur ores |
US20050118081A1 (en) * | 2003-09-30 | 2005-06-02 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
US20090013829A1 (en) * | 2003-09-30 | 2009-01-15 | Harris G Bryn | Process for the recovery of value metals from base metal sulfide ores |
US7736606B2 (en) | 2003-09-30 | 2010-06-15 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
US7968065B2 (en) | 2003-09-30 | 2011-06-28 | Jaguar Nickel Inc. | Process for the recovery of value metals from base metal sulfide ores |
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