CA1246345A - Processes relating to the extraction of metals from laterites and ocean manganese nodules - Google Patents

Abstract

ABSTRACT

A process is disclosed for the reduction leaching of metal values from iron oxide and manganese oxide containing ores. The leaching is effected under acidic conditions employing stabilized cuprous ions. The solubilized metal ions are selectively extracted with the cuprous ion solution being regenerated.

Description

~2~3~5 PROCESSES REL~TING TO THE EXTRACTION OF METALS
FROM LATERITES AND OCEAN MANGANESE NODULES

TECHNICAL FIELD
The processes of the present invention are in-tended for the treatment of certain ores, generally considered lower grade, as a result of which certain desirable metals can be extracted. One major ~ource of these ores includes the terrestrial oxide type nickel ores or laterites, so named because they result from a process known as laterization whereby ultramafic magma undergoes prolonged and continuous'decomposition and weathering.
After intense oxidation, differential leachings and precipitations and differential dissolution of magnesia and silica from the ultramafic rock, the residual surface layers of the deposit become enriched in nickel, cobalt, iron, chromium, manganese and aluminum. Further enrichment in nickel occurs in the underlying layers. As is known, a lateritic deposit, somewhat idealized, is characterized by a vertical composition profile with a hematitic cap or over-burden under which lies nickeliferous Limonite, followed by altered Peridotite and finally unaltered Peridotite.
As a general rule, cobalt, iron and manganese concentrations are higher in the upper regions of the vertical profile and decrease with depth. Similarly, nickel, magnesium and silica concentrations become greater as the depth increases. The Limonitic ore is particularly suited for treatment by the processes of the present inven-tion. It typically comprises a high iron phase, goethite (alpha-FeOOH) and a lower amount of manganese oxide. The goethite contains a high fraction of the total nickel content, e.g.~ 75 to 95 percent of the nickel and low fraction of the total cobalt content, e.g., 0 to 20 percent of the cobalt. The manganese oxide phase is roughly reversed with a high cobalt content, e.g., 80 to 100 percent of the cobalt and a lower nickel c ntent, e.g., 5 to 15 percent of the nickel. The overall result is that Limonitic ;~

~ 5873 ores provide a higher amount of nickel than cobalt.
Manganese ocean or sea nodules offer a composition generally opposite that of the Limonitic ores, that is, having a greater manganese oxide content than iron oxide content. Composition of the manganese nodules is analogous to what has been observed for the limonitic ores and that is a variance depending upon location in the ocean. Inasmuch as manganese nodules form in oxidizing environments, ca~ions with higher valencies predominate over reduced valence ' 10 stateS.
In order to access and extract, the nickel and cobalt, the ore matrix mu'st be treated chemically, that is, ' converted or solubilized. Commonly, this can be achieved by j reducing Fe(III~ to Fe(II) or Fe and MnO2 to Mn(II).
Thermodynamically, such reductions are possible by carbon monoxide or hydrogen in acidic or alkaline solutions.
However, kinetically, such reductions do not occur under reasonable temperature and pressure unless a catalyst is provided.
! 2Q Both laterites and manganese ocean nodules will be important as a future source for nickel and cobalt. The present invention is directed toward treatment of these and like ores which are generally considered to be low grade as well as not being amenable to conventional beneficiation techniques, e.g., nickel and cobalt content is too low for an economically feasible recovery. However, given high enough recoveries, such as greater than 90 percent, and low ' energy requirements, e.g., temperature at or near 30 to 60 C and pressure between l to 10 atmospheres, the processes set forth herein are economically feasible. An important process of the present invention shall be referred to herein ¦ as the ARIS process for Ambient Reduction by Intermediary Solutions.

BAC~GROUND ART
A variety of methods are known for the recovery of nickel and cobalt from lateritic ores. One method, known as ~ 3'~S 5873 the high pressure sulfuric acid leaching process, ~ , the Moa Bay process, is practiced by pulping the ore to specific mesh and solids and then selectively leaching the nickel and cobalt with sulfuric acid at elevated temperature and pressure. After proper washing and pH adjustment, the leached pulp is subjected to sulfide precipitation at elevated temperature and pressure to obtain the nickel and cobalt but not without oxidation, additional pH adjustment and selective recovery steps are performed.
The foregoing process is discussed in greater detail in a U.S. patent owned by AMAX, Inc., ~o. 4,044,096, which also employs a high' pressure sulfuric acid leaching step of laterites at elevated temperature. The ore is first slurried and autoclaved, leached with acid and subsequently discharged into a flash tank to create turbulence.
U.S. Pat. No. 3,761,566 provides another method for leaching lateritic ores. Leaching is conducted at elevated temperature and pressure with waste solutions of ferrous sulfate.
Similarly, processes ars known for the recovery of I nickel and cobalt from manganese sea nodules. U.S. Pat. No~
4,085,188 provides a reductive leaching of sea nodules in an aqueous ammoniacal medium and with a reducing agent such as SO2, sulfides, NO2 or metallic iron. Manganese is reduced from its tetravelent state to manganous carbonate and, nickel, cobalt and copper are extracted.
U.S. Pat~ No. 3,983,017 provides for the recovery of copper, nickel, cobalt and molybdenum from sea nodules by I leaching with an aqueous ammoniacal solution containing ¦ 30 cuprous ions. Carbon monoxide is employed as a reductant for cupric ions in order to regenerate cuprous ions for the initial leaching step.
Once metals have been solubilized they mut be removed from solution in order to complete the recovery process. Recovery preferably does not consume costly materials nor does it provide useless or waste by-products.
One process for the recovery of copper, silver and mercury 5~73 ~"0 . . .
- ~24~3'~
~ .
~ -4-is described in UaS~ Pat. No. 3,820,979 which calls for contacting an aqueous solution of the metal with a solution of a quinonic compound in an organic solvent. After the metal precipitates and is separated, the organic phase is separated and the quinonic compound is optionally reduced for subsequent use.
Another process for the recovery of copper from acidic solutions is set forth in my U.S. Pat. No. 4,038,070 which provides for reduction of cupric ions to cuprous ions with hydrogen i'n the presence of a cuprous stabilizing ligand such as acetonitrile to produce cuprous~nitrile complexes that can be dis'proportionated to produce copper metal and cupric ions.
A similar process which employs a quinolic 15 reductant is described in my U.S. Pat. No. 4,095,975 which also provides for the recovery of copper from acidic solutions. The copper solution is initially contacted with a quinolic reductant and an aqueous nitrile-solubilized in a water immiscible solvent to produce a nitrile stabilized cuprous solution and an organic solution of the oxidized quinolic compound. By driving off the nitrile, the cuprous ions disproportionate, producing equimolar quantities of copper metal and cupric ions. The quinolic compound can be reduced by hydrogen gas.
Notwithstanding the disclosures of the foregoing art, more economic processes for the selective extraction of desired metals such as nickel and cobalt have not appeared heretofore. Such processes should be characterized by low temperature and low pressure parameters and almost 30 quantitative recoveries. By-products are desirably neither harmful nor costly to generate or dispose. Recycling adds to the economy and is desirably accomplished without resort to expensive reactants or processing conditions. Again, the body of art known to me has not met all of these 35 requirements.

a634S

~-- 4a -SUMMARY OF THE INVENTION
The invention relates to a process for the extraction of ferrous, manganous and nonferrous metals from iron oxide and manganese oxide containing ores by reduction leaching comprising the steps of:
contacting the pulverized ore with a stabilized acidic cuprous ion solution cu~L in a suitable reactor at a temperature of up to about 90C while maintaining the pH between about 1.5 and 2.5 with acid to form a slurry, wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl-, X
being -H or -OH and R being aliphatic having from one to about four carbon atoms;
separating the slurry into a solid tailings portion and a pregnant liquor, the pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous metal ions;
selectively extracting the solubilized metal ions; and regenerating the cuprous ion solution from the solubilized cupric ions and the ligand, L in the presence of a reductant.
In another aspect of the present invention, there is provided a process for the regeneration of stabilized cuprous ion solution~, usable as reductants, from acid~c cupric ion solutions comprising the steps of:
dividing the cupric ion solution into first and second streams;
combining the first stream with a quinolic compound selected from the group consisting of quinol and anthraquinols to form a three phase slurry consisting essentially of free copper metal, an aqueous acid phase and the corresponding quinonic compound;
separating the quinonic compound from the copper metal and aqueous acid; and combining the second stream with the copper metal and aqueous acid and with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H

~;~463 ~5 - 4b -and -OH and R is an aliphatic radical having one to four carbon atoms, whereby the stabilized cuprous ion solution, Cu+L is formed.
In a further aspect of the present invention there is provided a process for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions~
comprising the steps of:
reducing the solubilized cupric ions with CO to form a slurry comprising copper metal, cupric ions and acid; and cooling and combining the slurry with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H and -OH and R is an aliphatic radical having one to four carbon atoms, to form the stabiliæed ion solution Cu'L.
In still a further aspect of the present invention, there is provided a process for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions comprising the steps of:
reducing the solubilized cupric ions with syngas in an autoclave operating at a pressure of between about 1.5 and 5.0 MPa and at a temperature of from about 150 to 280 C to form a slurry comprising copper metal, cupric ions, cuprous ions and acid; and cooling and combining the slurry with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H or -OH and R is an aliphatic radical having one to four carbon atomsS to form the stabilized ion solution Cu+L.

, ' i ., . .

~11 ~'3 A ~` ~

DISCLOSURE OF THE INVENTION
The present invention provides several processes employing various combinations of steps that either allow selective leaching of metal ions from various ores with intermediary solutions or the generation of such solutions.
The leaching processes are based upon an acid leach step employing stabilized cuprous ions and, in one instance, a combination thereof with ferrous ions. Leaching is con-ducted at low temperatures under 90 C and low pressures, under 1.4 MPa and at a pH of about 1.5 to 2.5.
A variety of ores can be treated as will be dis-cussed hereinbelow in gre'ater detail. Such ores basically comprise iron oxide and manganese oxide ores which provide nickel and cobalt, respectively. Nickel and cobalt recoveries from the ores, employing these processes, will ; usually equal or exceed 90 percent. The intermediary solu-tions employed produce no by-products harmful to the environment such as SO2, H2S, NO and the like. Generally the final waste materials will be inert and directly suitable for landfills.
In general, one process for the extraction of ferrous, manganous and nonferrous metals from iron oxide and manganese oxide containing ores by reduction leaching com- -prises the steps of contacting the pulverized ore with a stabilized acidic cuprous ion solution Cu L at a temperature of up to about 65 C while maintaining the pH between about j 1.5 and 2.5 with acid to form a slurry, wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl , X being -H or -OH and R being aliphatic having from one to about four carbon atoms; separating the slurry into a solid tailings portion and a pregnant liquor, the pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous metal ions; selectively extracting the solubilized metal ions and, regenerating the cuprous ion solution from the solubilized cupric ions and the ligand, L, in the presence of a reductant.
Additional steps of the first process include . , .
~2~3~i removing a portion of the cuprous ions from the cuprous ion solution after the step of regenerating by drawing off a slipstream of the stabilized cuprous ion solution, allowing the slipstream to disproportionate, forminy free copper S metal and cupric ions and, separating the copper metal from the cupric ions.
Alternatively, a portion of the cupric ions can be removed from the cupric ion solution before the step of reyenerating by combining the solubilized cupric ions with a quinolic compound selected from the group consisting of quinol, anthraquinols and naphthoquinols to form a three phase slurry consisting e~ssentially of free copper metal, an aqueous acid phase and the corresponding quinonic compound and, separating the copper metal therefrom.
A second major process of the present invention also provides for the extraction of ferrous, manganous and nonferrous metals from iron oxide and manganese oxide containing ores by reduction leaching and comprises the steps of contacting the pulverized ore with a stabilized acidic cuprous ion solution Cu L at a temperature of up to about 65 C while maintaining the pH between about 1.5 and

2.5 with acid to form a slurry, wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl , X being -H or -OH and R being aliphatic having from one to about four carbon atoms; separating the slurry into a solid tailings portion and a pregnant liquor, the pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous metal ions and, selectively extracting the solubilized metal ions.
Another process provided by the present invention can be employed for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions. It comprises the steps of combining the solubilized curric ions with CO as a stabilizing ligand and a quinolic com~ound selected from the group consisting of quinol, anthraquinols and naphthoquinols at a pressure of from about 0 10 to about 1.4 MPa and at a temperature of ~Z9L~;3~5 from about 20 to 90 C to form an aqueous CuCO+ lixiviant and the corresponding quinonic compound, separating the lixiviant from the quinonic compound and, regenerating the quinolic compound from the quinonic.
Another process for the regeneration of stabilized cuprous ion solutions from acidic cupric ion solutions comprises the steps of dividiny the cupric ion solution into first and second streams, combining the first stream with a quinolic compound selected from the group consisting of quinol, anthraquinols and naphthoquinols to form a three phase slurry consisting essentially of free copper metal, an aqueous acid phase and th'e corresponding quinonic compound, separating the quinonic compound from the copper metal and aqueous acid and, cooling and combining the second stream with the copper metal and aqueous acid and with a stabilizing ligand L, where L is CO or XRCN, whereby the ! stabilized cuprous ion solution, Cu L is formed.
Yet another process for the regeneration of stabilized cuprous ion solutions from acidic cupric ion 20 solutions comprises the steps of reducing the solubilized cupric ions with CO to form a slurry comprising copper I metal, cupric ions and acid and, combining the s~urry with a ¦ stabilizing ligand L, where L is CO or XRCN, to form the stabilized ion solution Cu L.
Still another process for the regeneration of t stabilized cuprous ion solutions from acidic cupric ion ; solutions comprises the steps of reducing the solubilized .
cupric ions with syngas in an autoclave operating at a pressure of between about 0.5 and 5.0 MPa and at a tem-perature of from about 150 to 260 C to form a slurry comprising copper metal, cupric ions and acid and, combining the slurry after cooling to below 90 C with a stabilizing ligand L, where L is CO or XRCN, to form the stabilized ion solution Cu L.
Any of the foregoing individual processes for regeneration of the stabilized cuprous ion solutions can be employed in conjunction with the two extraction processes ~ ~ 5873 63~

presented hereinabove~ Insofar as those processes are concerned, yet another manner for the regeneration, where L
is XRCN, includes the steps of combining the solubilized cupric ions with the ligand XRCN and a ~uinolic compound selected from the group consisting of quinol, anthraquinols and naphthoquinols at a pressure of from about 0.1 to about 0.2 MPa and at a temperature of from abou~ 20 to 65 C to form a CuXRCN lixiviant and the corresponding quinonic compound, separating the lixiviant from the quinonic com-pound and, regenerating the quinolic compound from thequinonic.
Still another ~ocess for the regeneration, in conjunction with the extraction processes, includes the steps of reducing the solubilized cupric ions with hydrogen to form a slurry comprising copper metal, cupric ions and acid and, combining the slurry with the ligand L, where L is CO or XRCN, to form the stabilized ion solution Cu L.
A separate process for the extraction of ferrous, manganous and nonferrous metals from iron oxide and manganese oxide containing ores by reduction leaching is provided which comprises the steps of contacting the pul-verized ore with a stabilized acidic cuprous ion solution Cu+L at a temperature of up to about 65 C while maintaining the pH between about 1.5 and 2.5 with acid to form a slurry, wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl , X being -H or -OH and R
being aliphatic having from one to about four carbon atoms, separating the slurry into a solid tailings portion and a pregnant liquor, the pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous metal ions;
; feeding the pregnant liquor to a second pulverized ore feed, containing, at least partially, manganese oxide ore to form a second slurry; separating the second slurry into a solid tailings portion containing sub~antially unsolubilized iron oxide ore and a second pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous ions and, selectively extracting the solubilized metal ions.

3~S

Finally, a process for the selective extraction of manganous and nonferrous metals from iron oxide containing ores by reduction leaching is provided which comprises the steps of contacting the pulveri~ed ore with an acidic Fe2 solution in a suitable reaction at a temperature of up to about 90 C while maintaining the p~ between about 1.5 and 2.5 with acid to form a slurry, separating the slurry into a solid tailings portion and a pregnant liquor, the pregnant liquor containing solubilized ferric, manganous, cupric and other nonferrous metal ions and, selectively extracting the solubilized metal ions.
~.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a schematic diagram illustrating a major overall process of the present invention, the ARIS process;
Fig. 2 is a schematic diagram illustrating an independent process for the regeneration of cuprous ion solutions with various stabilizing ligands which can be employed in conjunction with the ARIS process;
Fig. 3 is a schematic diagram illustrating an alternative independent process for cuprous ion regenera-tion which can be employed in conjunction with the ARIS
process;
Fig. 4 is a schematic diagram illustrating an alternative process for cuprous ion regeneration which can be employed in conjunction with the ARIS process;
Fig. 5 is a schematic diagram illustrating an alternative process for cuprous ion regeneration which can be emplo~ed in conjunction with the ARIS process;
Fig. 6 îs a schematic diagram depicting a process for the removal of copper from a process such as depicted in Fig. l;
Fig. 7 is a schematic diagram illustrating another process of the present invention for the reduction of ores;
Fig. 8 is a schematic diagram illustrating another overall process of the present invention for the reduction of ores; and ~ 3~5 5873 Fig. 9 is a schematic diagram depicting another process for the reduction of ores.

PREFERRED MODE FOR CARRYING OUT THE INVENTION
- 5 Practice of the present invention leaches or dissolves the Goethite phase, Fe3 OOH and Mn4 2 phase in laterites and similar iron ores to provide Ni2~ and Co2 by reducing the iron and manganese to Fe2 and M2 states. The -process wil also accomodate manganese sea nodules as the feed ore to reduce manganese and iron to 2+ states and provide Ni2 and Co2+ for subsequent separation and recovery. The ~arious processes employ a Cu /ligand ~) reductant and include steps for the regeneration thereof.
Before proceeding with the details of the processes, a brief discussion of the two ores particularly suited for treatment thereby shall be provided. First, regarding the laterites, the limonitic or high iron type is preferred.
Other ores, having a relatively high Mg and Si content, could pose process problems such as acid consumption and large quantities of magnesium by-products. A typical chemical composition by weight percent for limonitic ore appears in Table I.
As to the manganese sea nodules, any type can be treated by the process of the present invention irrespective of the ocean, depth, or the environment, e.g., seamount, ridges, continental borderlands and the like. An average chemical composition (partial), by weight percent, for sea nodules also appears in Table I.

~ 5873 3~5 TABLE I
Partial Chemical Composition of Feed Materials Elements Lat ritesa Mn nodulesb ! 5 Ni 1.20 0.491 I Fe 33.20 15.61 Co 0.15 0.30 Mn 0.48 16.17 Cr 1.67 0.001 Mg 7.25 1.82 Al 1.73 3.10 Si '8.93 8.62 Cu 0.01 ~.26 I

a) U.S. Bureau of Mines analysis of Gasquet Mountain Laterites b) Marine Manganese Deposits, G. P. Glasby ed., Elsevier Oceanographic Series, (1977).

The remainder of the ores will consist of various oxides, clay, minerals and the like many of which are neither useful nor necessarily recoverable by the process of the present invention. It is to be understood that as the iron, manganese, nickel and cobalt are selectively leached, the waste material or tailings become enriched in the unleached materials. Some, such as chromium, are not substantially removed by the present invention and therefore their recovery by alternative means from the tailings may be economically feasible, given the greater concentration therein.
The ARIS process constitutes a preferred mode of the present invention and is characterized by being a low temperature, low pressure acid leach process. Leaching of the Fe2O3 anc MnO2 ore components in acidic aqueous solu tions with the stabilized cuprous ions results in the accessibility of cobalt, nickel and copper with minimal leaching of chromium, magnesium and precious metals other 63~5i than silver. The cuprous ions in the leach solution are stabilized against disproportionation with a ligand L such as CH3CN, CO or Cl to form a complex. During the leaching step the cuprous ions are oxidized to cupric which can be recycled and regenerated as cuprous in several additional steps.
As noted hereinabove, the process is adapted for treatment of high iron-containing (limonitic~ laterites, which can contain some manganese, and manganese sea nodules, which also contain some iron. These iron and manganese ores contain non-ferrous metals such as nickel, cobalt and copper which can be extracted in'nearly quantitative yields.
Although particle size is not critical to practice of the present invention, it i5 generally understood in the art that a large surface area greatly reduces the reaction time and, therefore, the ore, terrestrial or sea nodule, is ground and milled by any suitable means to reduce the size to about -100 mesh.
The ore is first sub~ected to a redox leach step , 20 which occurs at a pH o~ from about 1.5 to 2.5 and preferably ; less than about 2. Non-oxidizing acids are employed such as sulfuric, hydrochloric and the like with sulfuric being preferred. The leaching step should be monitored as to pH
and additional acid provided on demand in order to maintain a steady and low pH.
The reducing agent for this step is the cuprous ion. Inasmuch as it is not stable in acid medium, it is complexed with a recyclable ligand such as CH3CN or CO.
~ While both are highly satisfactory, carbon monoxide is ¦ 30 preferred as will be discussed hereinbelow. The complexed ~, cuprous ion solution, designated at Cu Lx where L is the ! ligand and x is 1 or 2; can be provided from a separate supply in the processing stream. During the reduction leaching, it becomes oxidized to the cupric stage while iron and manganese are reduced. If desired, the cupric ions can be withdrawn from the system for other use or treatment or even discarded as waste; however, economics will most likely ~ 46~S ~ 5873 favor a recycling stream whereby cuprous ions are regenerated.
The overall redox leaching reactions for the two basic ores discussed herein are embodied in the following equations:
I Laterite (and Fe3 phase in Mn nodules) 2Fe3 OOH ~ (Cu LX)2SO4 + 3H2SO4 -ore redox leachant 2FeSO4 ~ 2CuSO4 + 4H2O + (Ni ,Co ~ + 2xL
pregnant liquor II Mn nodules (and M~n4 phase in laterites) Mn4 2 + (Cu Lx)2S4 + 2H2S4 redox leachant MnSO4 + 2CuSO4 + 2H2O + (Ni ,Co ) + 2xL
pregnant liquor Equations I and II could be modified as will be understood by those skilled in the art where hydrochloric acid is substituted for sulfuric.
¦ Moreover, as stated hereinabove the ligand L can also be Cl . Those skilled in the art will appreciate that an excess of anion is required to maintain copper soluble in the process solution and therefore excess hydrochloric ; acid or other chlorides such as MgC12 should be present.
While the work which is discussed hereinbelow exemplifies ¦ two of the ligands, CO and CH3CN, it is to be understood ! that Cl could also be employed and that the present inven-tion does not exclude this ligand.
After the appropriate time, the leached ore is separated as to liquids, solids and gases according to known engineering techniques. The ligand, CO or CH3CN is with-drawn in one stream for recyc.ing if desired; the pregnant liquor containing Fe2 , Mn2 , Cu2+, Ni2+ and Co2+ is with-drawn for extraction of nickel and cobalt and/or recycling of the other metals. Solid waste material is easily ~ 5873 ~, S

separated and discarded or separately treated for extraction of chromium and possibly precious metals such as Au, Pd, Pt and Rh wherever analysis indicates a sufficient content to make extraction feasible. Generally, the insoluble residue or waste will be enriched in these metals, as the process of the present invention does not solubilize them. One precious metal, silver, is solubilized where the ligand is XRC~. It can be removed by cementation with copper powder.
Regarding the regeneration of the cuprous ion reductant, the cupric salt from the redox leaching can be reduced with a quinolic compound, ~H~ which itself is oxidized to the quinone Q'according to the following equation:
III Regeneration of (CuL2)2 SO4 Reductant 2Cu SO4 + QH2 + 4L
(aqueous) (organic) (CUL2)2so4 + H2S4 Q
(aqueous) (organic) Alternatively, the cuprous ions can also be regenerated via H2 or CO or syngas, H2/CO, as will be discussed hereinbelow.
~ith reference now to the drawings and Fig. 1, the ARIS process shall first be broadly and schematically des-cribed and then be considered in greater detail, with other processes of the invention, in subsequent figures. The ore feed, laterite or manganese nodule properly ground, is contacted with the aqueous cuprous ion reductant in a reactor, 10. It is to be understood that the process can be conducted as a batch or continuously in co-current or counter-current tanks or as otherwise known, and that the selection of any particular reactor system does not constitute a limitation of the present invention. The leaching is done, in acid medium from a supply 11 with stabilized aqueous cuprous solution, stream 12. The cuprous solution can be provided from a recycling step, depicted in box 13.
Leaching time for laterites is approximately 45 minutes, for manganese nodules, it i5 about three minutes.
Leaching is conducted at low temperaturel on the order of ii345 from about 20 to 90 C, with 50 C being pre~erred.
Pressure is also low, ranging from atmospheric up to about 15 atmospheres ~1.5 MPa). Where the complexing ligand is CH3CN, atmospheric pressure is satisfactory in an atmosphere such as CO/H~ or other in order to exclude air. Where the ligand is C~, about 15 atmospheres or less is suitable to maintain the Cu solubilized to the desired concentrations.
The complexing ligand L can be withdrawn from the reactor 10 via stream 14 and fed to the recycling step 13 where it will be combined with the regenerated cuprous ions and returned to reactor 10 via stream 12. Withdrawal from reactor 10 is especially favored where L is CO.
The reduced slurry from reactor 10 passes via stream 15 and is allowed to separate and depressurize if necessary in separator 16. The complexing ligand L can also be recycled via stream 14 taken from separator 16 to box 13 and the solids portion or tailings passes via stream 17 for disposal or separate treatments such as for the recovery of chromium. While chromium recovery is not specifically provided for in this process, as noted hereinabove, greater concentrations in the tailings or waste may make recovery feasible. Stream 18 carries the pregnant liquor, e.g., Fe2 , Mn2 , Cu , Ni2 and Co2 as well as any Ag to box 19 where a step or steps for the extraction of iron, manganese, nickel and/or cobalt and/or silver is conducted. Such steps are known in the art and therefore are not specifically described.
The removal of these metal ions at box 19 will leave a separate aqueous stream 20 of cupric ions to be fed to box 13 for regeneration of the CUprOUQ ions, with a stabilizing ligand L. This is accomplished in 13 with a reductant from stream 21 and the recycle of the ligand via stream 1~. Before proceeding with a discussion of the regeneration process in box 13, it should be nc'ed that the various metals can be removed at other stages such as, by way of example, iron and manganese first followed by nickel and/or cobalt at another stage, or vice-versa.

46;~S

All of the pr~gnant liquor can also go to the regeneration step box 13 in which instance nickel and cobalt will pass ~hrough unchanged and can be extracted from stream 12 prior to reaching reactor 10. Iron could also be with~
drawn from stream 12 or retained with the cuprous ions and fed to ~eactor 10. Usefulness of ferrous ions in this manner will be discussed hereinbelow. The manganese ions would be of no use in reactor 10 and therefore should be withdrawn from stream 12 or before reaching step 13 in order to maintain maximum economy. It is to be understood that the patentability of the processes disclosed herein, as well as their operability, is hot dependent upon a particular mode or time for the extraction of Fe2 , Mn2 , Ni2 , or Co2 from solution. The processes make these metals available for extraction as they are leached from the ore feed and provide for regeneration of the stabilized cuprous ions for reactor 10 in all but one instance to be discussed hereinbelow.
Now, with respect to the lixiviant regeneration, cupric to cuprous, which has been depicted in step 13 of Fig. l! greater detail shall be provided by referring to Figs. 2-5 and the following explanation. In the regenera-tion step, the cupric ions are reduced to the cuprous state and the latter are combined and stabilized with the ligand L. Reduction of the cupric ions can be achieved in several manners and in Fig. 2 the use of a quinolic compoundr designated generally as QH2, shall be discussed first.
Quinol or hydroquinone, the dihydroxy alcohol of benzene, can be employed for the reduction step as can the anthraquinols, AQH2, and naphthoquinols, NQH2. Particularly useful quinolics are disclosed in U.S. Pats. No. 3,820,979,

4,032,331, 4,032,332 and 4,033,765i. These patents are directed toward the recovery of copper metal, Cu from cupric ions.
Quinolics, a term used herein for the foregoing compounds are organic and employed in a water immiscible .~ ' ' , ' , 63~S;

solvent mixture comprising non-polar compounds, e.g., aromatics such as alkyl toluenes and alkyl naphthalenes and polar compounds such as alcohols and various esters. As they react with cupric ions, they become oxidized to the quinonic species. The quinolic compound selected with the proper solvent mixture is fed via stream 25 to a reactor 26 as is the cupric ion stream 20 and the ligand via stream 14 or otherwise. The ligand L can be either a nitrile or carbon monoxide, as discussed hereinabove, or in the `I 10 instance of a separate process for treatment of cupric ions, both the ligand stream and the cupric ion stream can be ~ provided from sources oth~r than those resulting from the ', process depicted in Fig. 1.
Dealing first with the instance where L is a nitrile, and particularly acetonitrile, it is fed to the reactor 26 and very quickly combines with the cuprous ions i resulting from the reaction of the quinolic compound and the acidic cupric ions. The combination of the nitrile ligand XRCN, with cuprous ions in reactor 26 occurs under pressure 20 of from about 0.1 MPa to about 1.0 MPa at a temperature of from about 20 to 90 C. Reaction time is short, taking from about five to 20 minutes. The cupric ions are provided in an acidic aqueous solution, e.g., CuSO4 and therefore a --two liquid phase mixture occurs in reactor 26 and passes via stream 28 to a separator 29. The aqueous, acidic cuprous ligand portion becomes stream 12 of Fig. 1 which is fed to ` the first reactor 10 for ore reduction.
; The organic phase, which now comprises the --oxidized quinonic compound, designated herein as a shorthand notation for quinones, anthraquinones or naphthoquinones ¦ passes via stream 30 to a step 31 for regeneration of the respective quinolic, designated herein as QH2. Regeneration or reduction to the quinolic can be achieved with hydrogen gas over a conventional hydrogenation catalyst such as Raney nickel, or platinium or palladium supported on conventional supports at a pressure ranging between about 0.1 and 1.2 MPa and at a temperature of from about 20 to 80 C. The ~ 63~ 5873 .
~18-process of hydrogen reduction of quinones to their respec-tive quinols is otherwise known in the production of hydrogen peroxide and need not be ~urther detailed herein.
~he reduced quinolic, QH2 is fed via stream 25 to the reactor 26 as was discussed hereinabove. Alternatively, a fresh supply of quinolic, not ~hown, could be fed to the reactor 26 where its regeneration is not desired.
The entire ~tep of lixivi~nt regeneration 13 thus described is set forth in greater detail in my a~ore-mentioned U.S. Pat. No. 4,095,975. That patent teaches the recovery of copper metal via disproportionation of a cu L solution wherein L is acetonitrile. In addition to acetonitrile other nitriles, designated generally by the formula XRCN, can be employed where R is aliphatic having 13 from one to about four carbon atoms and x is -OH or H. Such examples include 2-hydroxy-cyanoethane, acrylonitrile and priopionitrile. These nitriles are disclosed in u.S. Pat.
No. 3,865,744. Leaching of laterites and sea nodules with a Cu CH3CN lixiviant is exemplified hereinbelow.
While R has been defined as an aliphatic having from one to four carbon atoms, other moeities having more than four carbon atoms are not necessarily inoperable or to be prec~uded. It has been recognized only that they may not be economic-~ly-practical and, therefore, an upper limit o~
four carbons has been recited.
Although the particular regeneration of cupric ions, stabilized with a nitrile ligand, may not be novel per se~ it is a step in the ARIS process and its use in con-junction with the redox leaching of ores is believed to be novel. In lieu of a nitrile ligand, L can also be carbon monoxide as discussed hereinabove. Where L is CO, the regeneration of cuprous ions from cupric by reduction with quinols is not known and is therefore novel ~s a separate process ~r in conjunction with the other ~teps of the ARIS
process.
B

3~5 The procedure to follow where ~ is CO is much like the foregoing description of Fig. 2, in that a quinolic is again employed, and therefore a total description shall not be repeated. The ligand CO can be provided via stream 14 from reactor 10 (Fig. 1). It is combined with the quinolic compound and aqueous acid cupric solution in reactor 26 under pressure of from about 0.1 MPa to as high as 1.5 MPa at a temperature of from about 20 to 90 C. Reaction is quick, taking from about five to 20 minutes. Where L is CO, a pressure in excess of atmospheric must be maintained, otherwise the ligand will escape and the cuprous ions will disproportionate to coppe~ metal and cupric ions. Reduction of cupric to cuprous is exemplified hereinbelow as is the leaching of lateritic ore with Cu CO lixiviant.
The foregoing regeneration of cuprous ions occurred in a one-step process, i.e., in reactor 26. A two-step regeneration is also possible with quinolic compounds and will be described with reference now to Fig. 3. Practice of this regeneration requires a division of the aqueous, acid cupric ion stream 20 into two streams 20A and 20B.
Generally, about 50/50 volumes will be suitable. Stream 20A
is reduced directly to copper metal in reactor 35 with a quinolic compound QH2 as disclosed hereinabove. In the absence of a ligand, the cupric ions are reduced directly to the metal according to the aforementioned U.S. Pat. No.
3,820,979. Stream 36 contains three phases: the organic --quinone Q with solvents, the aqueous acid H2SO4 from CuSO4 and, the solid copper metal powder. It is passed to a ~
separator 38 wherein the quinonic compound Q is transferred via stream 39 to a reactor 40 where it is reduced to the corresponding quinolic QH2 with hydrogen gas in the same manner as described in Fig. 2. The quinolic is then returned via str~am 41 to the reactor 35.
The remaining slurry from separator 38 comprising the aqueous acid and copper metal is fed via stream 42 to a second reactor 43 to which is fed stream 20B. In this reactor, the combination of cupric ions and copper metal ~ ~hZ~3~ `` 5873 with the ligand via stream 14 results in the generation of the stabilized cuprous ligand or stream 12 for the reactor 10 in Fig. 1. The foregoing two-step regeneration of cuprous ions stabilized with a ligand is belived to be novel alone as well as in combination with the other steps of the ARIS process.
Other two-step processes are also possible which do not utilize a quinolic compound. Such processes are set forth in Fig. 4, wherein hydrogen gas is utilized as the reductant and Fig. 5, wherein carbon monoxide is utilized.
With reference first to Fig. 4, the aqueous acidic cupric ion stream 20 is fed in a first step to an autoclave 50 to which is also fed hydrogen gas. This reduction is conducted at pressures ranging between about 15 and 50 atmospheres, at a temperature of from about 200 to 280 C and for about i 0.5 to 3 hours. In the second step, a slurry is fed, from autoclave 50, via stream 51, comprising copper metal, cupric ions and H (acid) to a reactor 52 wherein it is combined, after appropriate cooling, with a ligand such as ~' 20 from stream 14. The resulting stabilized cuprous ion Cu L
and acid H is provided via stream 12 to reactor 10 (Fig.
1). Although this particular regeneration of cuprous ions may not be novel per se, it is a step in the ARIS process and its use in conjunction with the redox leaching of ores is believed to be novel.
Before combining the slurry with the ligand, the slurry must be appropriately cooled to accommodate the particular type of ligand. Cooling to at least 90 C or under is necessary where the ligand is XRCN and cooling to at least 140 C or under is necessary where the ligand is CO. Such cooling is to be followed in the two-step regeneration processes without quinolics where hydrogen, carbon monoxide or syngas is employed.
With reference to Fig. 5, the aqueous acidic cupric ion stream 20 is again fed in the first step to an autoclave 55 to be reacted with carbon monoxide as a reductant, not primarily as a ligand. Reduction is again

5~73 ;3~5 high pressure and temperature on the order of 15 to ~0 atmospheres and from about 150 to 260 C for about 0.5 to 2 hours. A by-product gas stream comprising CO2/CO is evolved which can be suitably utilized or disposed. The reaction of CO with an aqueous solution of CuS04 at elevated temperature (140~ to 150 C) and pressure has been described as a minor side reaction by E. Peters, T. Kurnsawa, F.
Loewen and M. Nishitani in a paper entitled "A Carbonyl-j Hydrometallurgy Method for Refining Copper" presented at the Joint Meeting of MMIJ-AIME 1972, Tokyo, Print No. T IV c4.
The reaction is as follows:
IV 2Cu + 3CO + H'2O ~ 2CutCO) + CO2 + 2~
Some stabilized cuprous ions result as CuCO , along with some copper metal and cupric ions. This slurry is allowed to cool to a temperature of at least about 140 C or under, as it passes via stream 58 to reactor 59 where, ! in the second step, it is combined with carbon monoxide as a ligand~ Again, the stabilized cuprous ion stream 12 results. The CO ligand supply could be provided from stream 14, recycled from reactor 10 (Fig. 1) or independently.
The foregoing two-step regeneration of cuprous ions is believed to be novel alone as well as in combination with the other steps of the ARIS process. It is to be understood that a combination of Figs. 4 and 5 could also be practiced utilizing H2/CO or syngas as yet another novel reduction step for the regeneration of cuprous ions for the ARIS process. Inasmuch as the latter would merely be a combination of the foregoing descriptions, a detailed dis-cussion thereof is not deemed necessary.
Having described several of the possible regenera-tions of Cu ions stabilized against disproportionation with CO or C3CN and the like, it should be noted that dispro-portionation may be desirable, to a degree, in the ARIS
process. Recognizing the ~ide variety of compositions represented by laterite and manganese ores, it is possible that some copper compounds can be present. As a result of the leaching in reactor 10, these become freed as Cu2 ions 2~63~S

and subsequently reduced to Cu ions in step 13. After a period of several recyclings via stream 12, the copper ion content would build up to an undesirable concentration.
Thus, at least one manner by which to control the amount would be to allow a portion of the stabilized ions Cu L to disproportionate, producing copper metal and cupric ions approximately in equal amounts. A bleed streaml for i instance, could be drawn off of stream 12, as is depicted in Fig. 6. There, stream 60 will remove a predetermined amount necessary to reduce the overall flow of copper through the process where new copper is continuously being leached and added. Stream 60 is fed ~to a suitable processing step 61 where the ligand L is removed either to recycle stream 14 or ¦ for other use or handling. Copper metal is removed via stream 62 and cuprous ions are returned to stream 12 via stream 63.
Removal of the ligand in step 61 is conventional;
for CO depressurization will result in disproportionation while for an organic nitrile, distillation of the ligand will destabilize the Cu ions. It is to be appreciated that the bleed stream 60 can comprise other components as only the cuprous ions will be affected. Alternatively, other processing steps can be employed for excess copper removal such as, electrolytically or cementation with iron metal.
Also, the point of copper removal is not necessarily limiting on the practice of the present invention. One other step could be the reduction of Cu~ to Cu, as depicted in Fig.
3, with a quinolic so long as the copper metal was not --subsequently treated in reactor 43 to form Cu L.
Thus far, the ARIS process has been described ! wherein stabilized cuprous ions in acid medium are utilized to leach lateritic ores and manganese sea nodules and, wherein the cuprous ions are regenerated. More broadly, a modification of the ARIS process is also contemplated as is next described with reference to Fig. 7. The process is comparable to that discussed with reference to Fig. 1 except regeneration of the cuprous ions is not included.

3~5 Crushed ore is again fed to the reactor 10 with a supply of acid to maintain a steady pH. Stabilized cuprous ions are provided from an independent source 60 via stream 12. If ~he ligand is CO, it can be vented from reactor 10 via stream 14 and suitably handled. The slurry from reactor 10 is fed via stream 15 to the separator 16, where nitrile ligands are removed by stream 1~, solid tailings and the like pass via stream 17 and the pregnant liquor passes via stream 18 to a suitable processing step or steps~ box 19 where iron, manganese, copper, nickel and/or cobalt can be extracted as desired. Reaction conditions such as temperature, pressure and pH are the s'ame as set forth hereinabove for the description of Fig. 1.
Another modification to the ARIS process exists where ferrous ions Fe2 with the cuprous ions previously described are employed in a leaching step, e.~., reactor 10 or other. It will first be recalled that ferrous ions result from the leaching of laterites in reactor 10 with the acidic cuprous ligand solution, stream 12. Ferrous ions would be useful on a feed stream of manganese sea nodules or a terrestrial manganese ore. An instance of the latter could be drawn from a lateritic deposit which is most often characterized by a vertical composition profile. Whereas the nickeliferous Limonite is preferred for the feed to reactor 10 with a cuprous ion reduction, the overlying hematitic cap is often more concentrated in manganese which, in turn, will carry a higher content of cobalt.
Inasmuch as the ferrous ions can only leach a manganese ore, that ore is the only instance where cuprous 3~ and ferrous solutions could be combined. If, for instance, the cuprous and ferrous solutions were employed on a lateritic ore, the cuprous ions would selectively leach first the manganese portion, this being preferred to cuprous attack of the Fe2O3 phase as well as ferrou; attack of the MnO2 phase. In a short time, the manganese phase would be reduced, leaving no ore for the ferrous ions which, of course, will not react with the Fe2O3 phase.

~- 5~73 24~39~S

With the foregoing as a background, reference to Fig. 8 should now be made wherein this embodiment will be further developed. A lateritic ore feed, Lat(a), is fed to a reactor 70, comparable to the reactor 10, via str~am 71.
The lixiviant solution is provided via stream 72 and includes acidic cuprous ions, properly stabilized, com-parable to stream 12 (Fig. 1) and ferrous ions Fe2+(c) from a separate source. The latter ions are optional and will be employed primarily in a second, separate leaching step set forth hereinbelow. Temperature, pressure and pH for this step is the same as was disclosed in conjunction with the description of Fig~ 1. A'-slurry results which is fed via stream 73 to a separator 74. Solids or tailings exit via stream 75 for the desired treatment, disposal or other handling and are essentially free from Fe and Mn. Meanwhile, the pregnant liquor, stream 76, is fed to a second leach reactor 80. The pregnant liquor comprises Mn (a) ions and Fe2 (a) ions from Lat(a) and Fe2 (b) and Fe2 (c) ions.
Co2+(a) and Ni2 (a) also result but have been omitted from the drawing to simplify the latter.
Into reactor 80 is also fed, via stream 81 a second lateritic ore, Lat~b) and/or manganese ore (c), sea nodules or terrestrial. The leaching that will occur will be based only upon Fe2 ions, Fe2+(a), (b) and (c), inasmuch as no Cu ions are left over from reactor 70 or otherwise fed into 80. Reaction conditions include the same tempera- -ture range of 20 to 90 C, a pressure ranging from ambient to about 0.3 MPa and the same overall pH. The resulting --slurry passes via stream Bl to separator 82. Where the Fe2O3 portion of laterite (b) contains desirable amounts of Ni, the stream 83 can carry the solids, essentially unreacted~ and tailings to the first reactor 70 where they can be reacted with the Cu ions. If the Ni content is too low or otherwise undesirable, stream 83 can be discarded (not shown). The pregnant liquor stream 84 now comprises Cu2 ions unchanged from the first redox leaching, reactor 70, Fe3 ions from the leaching reaction, Mn2 ions from ~4 ....

laterites (a) and (b) as well as the m~nganese ore feed (a).
The Mn ore having been solubilized, Co2 (b) ions will now also be present but again, do not appear in the drawing.
It will be appreciated from discussions pertaining to the other flow diagrams, that separations of the accessed Ni2+ and Co2+ ions could have been inserted into the process depicted in Fig. 8 and any convenient stage such as off of streams 7S, 83 or 84. Similarly, the Cu2 ions could have been recycled for Cu+ regeneration, per Figs. 2~5, at any of these streams.
Of course, variations of the process set forth in Fig. 8 are contemplated w~thin the scope of the present invention. Thus, while Fig. 8 depicts a second leaching step to be utilized in conjunction with the ARIS process set forth in Fig. 1 or the modified process set forth in Fig. 7, i.e., no Cu ion regeneration, it is entirely possible that the leaching in the second reactor 80 could comprise an independent process for the selective leaching of iron oxide containing ores which will be briefly discussed with reference to Fig. 9.
Reactor 90 is there fed, via stream 91, an ore having a useful content of manganese which, in turn, carries a desirable amount of cobalt. Such ores were discussed with reference to Fig. 8 and need not be repeated here. However, it should be borne in mind that the process of Fig. 9 is one that can be employed as a selective leaching of laterites - -and the like where it is desirable to extract only the cobalt. An acidic leach solution comprising Fe2+ ions is --fed via stream 92 and produces a slurry, stream 93 which is fed to a separator 94. Again, solids comprising unreacted Fe2O3 and tailings exit via stream 95 for desired handling and a pregnant liquor stream 96, is drawn off containing Fe3 ions from the leaching, and solubilized ~n2 , Ni2 and Co2 for further separation in box 98 and/or use as desired.
Although not specifically shown in combination with Fig. 9, any Fe2O3 content could then be fed to a series of steps as provided in Figs~ 1 or 7 wherein lateritic ore 3 ~

feed is treated with Cu ions. The latter would constitute a two-step differential leaching techni~ue whereby the manganese and a high concentration of cobalt was first accessed and then the iron with a high concentration of nickel followed.
A reduction of a laterite ore, employing Fe2 ions and inert Cu2 ions selectively to leach Co and Mn has been provided hereinbelow as Example No. 25, reported in Table X.

General Leaching Procedure In the several examples which are detailed herein-below, leaching of laterites was carried out in a 500 ml jacketed glass reactor which was provided with a stirrer~ pH
electrode, thermometer, refluxing condenser, sampling port and a nitrogen gas sparging tube, as well as an inlet for acid addition. The temperature in the flask was maintained at within + 1 ~ by circulating water from a thermostated bath into the jacket of the reactor.
A pH controller was employed to monitor and maintain the desired constant pH during the leaching experi-ments. A peristaltic pump, activated by the pH controller, was used to add a (50:50 by volume) solution of H2SO4/H2O
into the reactor during the course of the redox leaching experiments. The total amount of added acid solution was measured at the end of each experiment.
Nitrogen gas was passed throughout the reactor at -~
a low flow rate, however, a complete exclusion of air during these preliminar~ experiments was not attempted. Solution ~~
samples were taken at various time intervals with a 5 ml pipette through a ground joint opening in the reactor cover at which time air was free to diffuse into the reactor. The stirring was stopped and the slurry allowed to settle for one minute before the sample was withdrawn. The 5 ml sample was talen from as close to the surface as possible to minimize the amount of solids withdrawn. The amount of solids taken with the sample was small and not measured~
however, the concentrations obtained and reported herein are -~ 5873 2~3~5 somewhat lower than the actual ones due to the presence of these small amounts of solids in the samples taken. The samples taken were immediately "quenched" in an acidic solution containing H2O2 as an oxidant for cuprous and ferrous ions and brought to 100 ml total volume. Within five minutes, part of this solution was filtered to yield two parallel samples of about 25 ml each. These were then labeled ~or ready identification.
All samples taken and prepared in the above manner were analyzed by Atomic Absorption Spectroscopy. The con-centrations of nickel, iron, cobalt, manganese, chromium, magnesium, silicon and al~minum in the leach solution at various sampling times were calculated from the analytical results.
The general procedure for each series of redox leaching experiments was as follows: The measured amount of cupric sulfate solution, at the desired pH, was introduced first into the reactor flask and allowed to reach the selected operating temperature while stirring and purging with nitrogen to displace air from the reactor, and most of the dissolved ox~gen. The calculated amounts of copper powder and acetonitrile were then introduced into the reator and stirring continued until the copper powder dissolved completely. Dissolution of copper powder yielded the desired stabilized cuprous lixiviant for the redox leaching Of ore.
The stirring was then stopped and the weighed amount (50 g) of laterite was added into the cuprous solu- --tion. This addition was completed within three minutes after which stirring commenced. While some reaction took place during this addition time, time zero for the redox leaching was considered to coincide with the time when stirring commenced.

Leaching of Laterites with Cu (CH3CN)x Examples No. 1-9 Gasquet Mountain laterite, having the composition reported in Table ~ hereinabove, was leached with the ~24L~i3~S

-~8-Cu (CH3CN)x lixiviant in Examples No. 2-9 discussed herein-below~ 50 g samples of -100 + 150 mesh dry screened laterite was treated with the leach solution and under the conditions found in Table II. The copper reductant solution was made by dissolving 11.66 9 of copper metal in 382 ml of water (unless otherwise specified) containing 0.257 moles of CuSO4, to which 59 ml of CH3CN (unless otherwise specified) was added. Total volume of all but one solution was 441 ml.
The initial concentration of cuprous ions, approximately 0.83M, was calculated and fixed to a 20 percent excess over that stoichiometrically necessary to reduce all Fe(III) and Mn(IV) to Fe2 and Mn2 , '-This concentration was employed for Examples 2-8, half the concentration was employed for Example No. 9 and zero for Example No. 1, a control, where leaching was conducted in the absence of the active cuprous ions. Concentrations of metal ions at different sampling times ranging between three to as many as 420 minutes appear in Table III.

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~ ~2463~5 5873 TABLE III
Metal Ion Concentrations (~m) as a Function of Leachlng Time for Examples 1-9 Example Rxn time No. (min) Ni Fe Co Mn Cr . 30 670 12850 212 584 54 : 330 956 ' 23500 224 576 112 i 4 4 516 7700 164 - 30 : 30 830 16500 206 - 86 330 1058 25550 230 57q 160

6 3 220 760 200 574 4

7 3 388 4065 224 590 20 572 g648 226 586 4~
' 210 1042 .25745 230 544 150 i 8 3 306 1897 212 538 10 i 9 3 184 1376 106 292 8 270 564 11910 1'~7 298 72 ~ 2~63~5 5873 -31~

With reference to Table III, it will readily be noted that a signiicant amount of the metals Ni, Fe, Co and Mn were leached from the laterite ore with the Cu CH3CN
lixiviant as compared to Example No. l where the copper reductant was not employed.
Decreasing the reaction temperature to 25 C, Example No. 31 resulted in a corresponding decrease in metal ion yields over other examples, conducted at 45 C. On the other hand increasing the temperature to 65 C, Example No.
4, did not significantly affect the yields thereby demon-strating that the process can be conducted at relatively low temperatures, such as 45OrC.
The effects of pH between 1.5 and 2.5 and concen-tration of the copper reductant solution is also demonstrated in Table III. Generally, pH did not dramatically effect the leaching between l.5 and 2.0, Examples No. 2 and 5, while increasing it to 2.5, Example No. 6, did decrease the yields. Reduction in the CH3CN addition, Example No. 7, did not appear to effect yields, neither did dilution of the reductant, Example No. 9 did as long as at least the stoichiometric amount of Cu was supplied.
Analysis of the metal ion concentrations reported in Table III also establishes that the leaching process of --the present invention is highly selective insofar as most of the Ni, Co, Fe and Mn is leached from the ore while most of the Cr remains with the leach residue or tailings. It can --~
readily be noted that about three times the Ni and l0 times the Fe content were accessed in Examples 2-9 as compared to ~~
Example l, while Cr content remained relatively low in the pregnant liquor. In this manner, the tailings will be certain to carry a higher weight percent of Cr than the original ore, making recovery more economically feasible.
By selecting the right combination of temperature pH and leaching time it is possible to opitmize the extrac-tion of Ni and Co versus Cr. Drawing from specific examplesreported in Table III, namely Nos. 2-6, exemplary optimiza-tion can be demonstrated as has been reported in Tables IV and V

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At a ~onstant pH of 2.0 the lowest amount of Cr leached occurred where leaching continued for 30 minut0s.
Where greater times of 60 and 330 minutes were provided, some increase in Ni was observed but very little increase in Co. Temperature also had little effect of Co, but signifi-cantly greater effect on Cr and Ni. Maintaining a steady temperature, all three metal extractions generally increased as pH decreased (the solution was more acid), except for Co at 330 minutes.
A similar comparison can be made by examining the concentration ratios of Ni/Cr and Co/Cr at various sampling times provided in Table ~..

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The highest Ni/Cr concentration occurred at the lowest temperature and pH of 2.0 and decreased as the tem-perature rose. Increasing the pH, Example No. 6, improved the ratio at 45 C. The best Co/Cr concentrations were also obtained at the lowest temperature or highest pH.
A measurement of acid addition (H2SO4) versus metal ion solubilization was also examined and is reported in Table VI for a separate example, No. lOo The condi~ions for Example No. 10 were those employed for Example No. 2, but 50 9 of -100 + 150 mesh wet screened laterite was leached rather than dry screened.

TABLE VI
Acid Addition During Leach Reaction Time Conc. H2SO4 Ex. No. (min) (ppm) Ni Fe Co Mn tg) 10 3 444 3000 294 7622.7g 30 642 12060 298 76619.77 2090 712 15640 290 74~24.86 Separate analyses of the metal extraction data revealed that the addition of acid beyond a certain point, --e.g., 20 9, would not increase the extraction of Ni but would contribute to further dissolution of Fe and Cr.
In order to determine the efficiency of the ---present process, more specifically when the Cu CH3CN lixi-viant is employed, a separate evaluation was conducted --employing a two stage leaching.
A 50 gram sample of the laterite ore, -100 + 150 mesh dry screened, Example No. 11, was leached with the solution and under the conditions reported for Example No. 4 hereinabove for a total of 330 minutes. This solution was filtered and the leach residue collectc-d. This residue was then subjected to a second leaching step, identical to the first for 90 minutes after which the remaining leach residue was filtered and washed. This second residue was then ;3~5 digested with aqua regia to determine metal values not leached.
The laterite feed material was similarIy digested and analyzed following which a mass balance was then con-S ducted and the results were used to calculate the percentrecovery, or eventually solubilization for Ni, Co, Fe, Mn and Cr. The values were as follows: Ni 95.4%; Co 98.3%; Fe 97.2%; Mn 98.4%; and, Cr about 10 to 20%.

Leaching of Manganese ore with Cu (CH3CN) Having established the usefullness of the Cu (CH3CN) lixiviant with laterite o~e, further evaluations were con-ducted to demonstrate the ability of this material to reduce manganese sea nodules.
The reactor employed was similar to the one dis-cussed hereinabove in conjunction with the laterite leaching examplec, except that it had a 500 ml capacity and improved, high speed stirrers. Pacific ocean manganese nodulesl -150 ~ 200 mesh dry screened were employed and three exemplary ! 20 experiments were conducted. Example No. 12 was a control or blank where no Cu (CH3CN) was employed. Examples No. 13 and 14 represent practice of the present invention.

! Example No. 12 I

44.2 g of CuSO4 were dissolved in 225 ml of H2O and the pH was adjusted to 2.0 by the addition of the same ---H2SO4:H2O mixture (50:50 vol). The solution was added to the glass reactor under N2 purge and maintained at a con- --stant 45~ C. Then, 25 9 of the manganese nodule was added with 100 ml H2O. Stirring commenced at time zero and acid was provided on demand to maintain the pH at 2Ø 5 ml i samples of solution were withdrawn at various times, diluted to 100 ml with H2O/acid, filtered and analyzed by atomic absorption. After 90 minutes, the solution was filtered and 290 ml thereof were collected. Metal ion concentrations appear in Table VII with values for Examples No. 13 and 14.

~f4~3~ 5873 Example No. 13 Utilizing the same reactor as for Example 12~ 24 9 of CuS04 were dissolved in 250 ml of H20 and the pH was adjusted to 2Ø The solution and 8.0 9 of Cu metal were added to the reactor under N2 purge. The reactants were ~ vigorously stirred at 45 C under refluxing conditions.
¦ Next, was added 48 ml of CH3CN with acid on demand to main-tain pH and generate the cuprous lixiviant. Finally, 25.0 9 of manganese nodules was added with 50 ml of H20 at time ~-ero. 5 ml solution samples were again withdrawn at various . times, diluted to 100 ml with H20/acid, filtered and ; analyzed. After 90 minutes, 415 ml of filtered solution remained.

~ 15 Example No. 14 ¦ This procedure was conducted as the previous one except the addition of 25.0 9 of nodules was with 25 ml of H20. Supply of H2S04:H20 was not fast enough to maintain pH
which did rise to 3.8 upon addition of the sea nodules. It was returned to 2.0 after 15 minutes although by then the reaction was substantially complete.

~ .

~- - 5873 3at5 ~38-TABLE VII
Redox Leaching of Manganese Sea Nodules with Cuprous Aeetonitrile Example No. 12 13 14 Time Element(min) Mn 3 0.192 4.64 10.78 g/l 10 0.230 - , 14.64 - 10 15 - 10.5 0.240 - 15.34 ~0.258 - 15.36 0.264 10.68 15.32 Fe 3 0.088 2.42 6.18 9/1 10 0.119 - 9.94 - 5.98 0.131 - 10.62 0 ~ 142 ~ 10 r 96 0.135 6.24 11.02 Ni 3 6.0 177.6 386 ppm 10 10.6 - 544 - 412.0 19.2 - 570 -29.4 - 566 37.0 428.0 578 Co 3 1.2 29.6 64 - -ppm 10 1.4 - 80 ~ 59.4 1.4 - 81 1.8 - 78 2.2 60.0 79 Co 3 1.2 29.6 64 ppm 10 1.4 - 80 - 59.4 1.4 - ~1 1.8 - 78 2.2 60.0 79 ~4~3L~5 5873 The leach residue from Example No. 14 was digested in aqua regia and the solution analyzed by atomic absorp-tion~ The Mn nodule feed material was also subjected to this digestion and analysis. Mass balance calculations showed the following percent solubilizations by weight: Mn 99.9; Fe 94.3; Ni 99.4; and, Co 99.6.

Leaching of Laterite with Cu(C0) Acidic Solution Two experiments were conducted and evaluated utilizing Cu(C0) for the reduction of a laterite ore as follows: '`

Example No. 15 Into a one liter autoclave was charged 39.5 g CuS04, 5.24 9 of copper powder and 550 ml of water. The mixture was purged with C0 to remove air and the pH was adjusted to 1.5 using H2S04/H20 (50:50 vol). The reaction was stirred at 45 C under a C0 pressure of 175 psig (1.21 MPa) for four hours in order to insure complete dissolution of the copper metal.
Next, 500 ml of the cuprous solution formed in the first autoclave (A) was transferred to a two liter autoclave --(B) by pressure differential under C0. Autoclave B con-tained 25 9 Gasquet mountain laterite, -270 mesh wet screened, at 45 C and 75 psig (0.52 MPa) C0. When the - -transfer of solution from autoclave A to B was completed, stirring in B commenced as did leaching of the laterite and --time zero was established. Total C0 pressure during leaching was maintained at 1.21 MPa and the acid/water solution was added on demand to maintain pH at 1.5. The pH
probe monitoring device failed after 30 minutes and there-fore acid addition was discontinued. At the end of the leaching, the contents of B were filtered. Solids content was 11.~ 9 wet; filtra~e collected was 500 ml.

463~L5 Example No. 16 The procedure followed was identical to that for Example No. 15 except that 20 9 of Gasquet laterite was leached in Autoclave ~. The pH probe functioned properly and total acid/water addition on demand, 50:50 volume, was 11 9. The pH drifted from 105 to 1. over the total leaching time.
Metal ion concentrations were measured by with-drawing 5 ml solution samples from Br Each sample was quenched in H2O (acidic) containing a small amount of hydrogen peroxide and then diluted to 100 ml. Each solu-tion was analyzed after f'iltration, by atomic absorption spectroscopy. The metal ion concentrations for Fe, Ni, Mn and Co at various times in minutes from time zero were measured and have been reported in Table VIII. Concen-trations for Fe were 9/1 while for the other four metals ppm has been indicated.

TABLE VIII
Metal Ion Concentrations Following Laterite Leaching with Cu(CO) Time Fe Ni Mn Co Cr --Ex. No.(min) g/l ppm 3 5.45 134 103 33 30 9.52 251 164 57 56 --~
12.70 315 182 62 74 19.14 364 234 79109 120 20.70 400 2~2 80117 16 3 1.12 67 131 45 11 1.84 101 175 64 13 4.78 175 264 92 22 6.46 214 192 65 31

8.76 236 1~0 64 40 120 11.18 314 212 73 ~9 k~ 46 3 ~ 5 5873 Again, it can be observed that the leaching process produced large amounts of Fe and Ni, apparently less Mn and Co but nevertheless high values because laterites are low in these values and, little Cr.

Reduction of Cu to Cu (CO) j As has been developed hereinabove, the process of the present invention employs cuprous solutions to leach laterites, manganese sea nodules and similar ores. These 10 can be generated by any suitable means including those disclosed herein. At least one novel and preferred method for preparing the cuprous'`reductant is set forth herein and f it involves the use of a quinone Q, as disclosed herein-; above.
General Procedure In the examples which follow, the given anthra-quinone AQ was first dissolved in a solvent mixture of polar and non-polar organic solvents. The ratio of each is 20 optimized for the maximum solubility of both the anthraquinone and its corresponding anthraquinol and thus, neither the solvents nor the specific amounts should be construed as limiting. -The organic solvent mixture was introduced into a 25 first autoclave followed by the addition of a hydrogenation catalyst such as 5% Pd on A12O3. Air was displaced with an --inert gas Ar, although He, N2 and the like could be sub-stituted. Pressure was increased to 125 psi (0.86 MPa) with ~~
stirring and heating to 50 C. Hydrogen gas was introduced 30 to a total pressure of 175 psi (1.21 MPa) and was maintained ¦ by periodic addition.
The desired volume of reduced organic material was transferred from ~he first autoclave to a second under pressure. The liq id organic was transferred from the first 35 autoclave through a dip tube equipped with a filtering element in order to retain the hydrogenation catalyst. The second autoclave contained an aqueous acidic cupric sulfate L 6 3 ~ S

solution at a given pH, temperature, copper concentration and volume and under a CO pre ssure. Time zero for the reaction commenced with stirring of the transferred organic and aqueous solution with CO gas.
5 cc samples of aqueous phase were taken at time intervals indicated in Table IX. These were then oxidized with an acidic FeC13 (lM) 25 ml solution which was titrated with a cerric ammonium sulfate solution to determine ferrous ion. From this, the concentration of cuprous (generated) versus time in the autoclave ~as calculated and the total copper concentration was determined by atomic absorption spectroscopy.

Example No. 17 15 Organic (Autoclave 1) 60% vol xylene 40% vol 2-ethyl-1-hexanol 49 g/l 2-ethyl anthraquinone 550 ml of organic reduced with H2 over 5% Pd (1 g) on A12O3 in autoclave 1 at 472 ml of organic transferred to autoclave 2 Aqueous (~utoclave 2) 125 ml CuSO4 solution, [Cu] = 75.0 g/l pH = 2.0 T = 50 C
125 psig CO (0.B6 MPa) After transfer of the organic, the total pressure was increased to 225 psig (1.55 MPa) with CO and maintained. --Example No. 18 Organic Same as for No. 17, except 500 ml transferred to autoclave 20 Aqueous Same as for No. 17, except CO pressure was maintained at 150 psig (1.04 MPa).

i345 Example No. 19 Organic (Autoclave 1) 3000 ml xylene 1000 ml isobutyl-heptyl-ketone 220 g 2-t-butyl-anthraquinone 5S0 ml of organic reduced as in Example No. 17 485 ml of organic transferred to autoclave 2 Aqueous (Autoclave 2) 250 ml CuSO4 solution, ICu] = 48.6 g/l pH = 2.0 T = 50 C
50 psig CO (0.35 MPa) After transfer of the org~anic, total pressure was increased to 150 psig (1.04 MPa) with CO.

Example No. 20 Organic Same as for No. 19, except 495 ml transferred to autoclave 2.
Aqueous Same as for No . 19, except 167 ml volume of CUSO4.
Example No. 21 Organic Same as for No. 19, except 495 ml transferred to autoclave 2. --Aqueous Same as for No. 19, except 125 ml volume of CuSO4.

Example No. 22 Organic Same as for No. 20, except 495 ml transferred to autoclave 2. 0 Agueous Same as for No. 19 Total CO pressure, 225 psig (1.55 MPa).

Exa-mple No. 23 Organic Same as for No. 19 except 500 ml transferred to autoclave 2.
Aqueous Same as for No. 19 except 167 ml volume of CuSO4.
Total CO pressure, 225 psig (1.55 MPa).

^~ *~ ~4~3~ 5873 At the end of the reduction, the aqueous solution was color-less indicating almost total reduction to Cu .

TABLE IX
Cu+ Concentration (9/13 versus time Example Nos.
Time (min) 17 18 19 20 21 22 23 2 11.3 10.73.8 8.2 1S.37.3 20.3 26.4 27.09.515.1 30.819.4 34.6 39.4 42.917.8~20.8 49.935.4 50.8 51.8 62.827.922.1 49.738.7 50.2 As can be seen from Table IX, the highest cuprous concentrations were observed for Examples 17, 18, 21 and 23 with acceptable concentrations occurring ater only 20 minutes.

Selective leaching of Co, Ni and Mn from Laterite with Fe /Cu acid solution As stated hereinabove, the pregnant liquor from the first step of the ARIS process for the leaching of laterites contains reduced iron Fe2 and oxidized copper Cu2 . This material could be employed to reduce manganese from a fresh supply of ore which also results in the -dissolution of cobalt. In the work which is discussed next, two experiments were conducted to demonstrate the use of --this reductant solution. The first, Example No. 24 con-stitutes a control or blank with Cu2 and H2SO but no Fe2 . The second example, No. 25, employed Cu~ , H2SO4 and Ee2 which was added to simulate the pregnant liquor from the first step of the ARIS process.
The following ingredients were dissolved, stirred and heated in a 500 ml jacketed glass reactor at 45 C with the necessary addition of H2SO4 to maintain a pH of 2Ø
Example ~o. 24: 341 ml H2O plus 70.3 9 CUSO4; Example No.
-~ 63~S 5873 25: 341 ml H2O plus 70.3 9 CuSO4 plus 61.3 9 FeSO4.
At time zero, 50 g of Gasquet laterite, -270 mesh wet screened plus 100 ml of H2O were added to each reactor.
~amples were taken and analyzed as previously described and ! 5have been reported in Table X all concentrations being ppm.

TABLE X
Leaching with Fe2 /Cu2 Acid Solutions !

Time Example No.
Element (min) 24 25 Co 3 '~ 12.40 154.00 13.60 144.00 17.60 156.00 120 22.20 146.00 Mn 3 37.20 486.00 40.00 482.00 47.40 498.00 120 58.00 492.00 Ni 3 50.40 188.0 66.00 220.00 99 00 248.00 120 133 80 260.00 Clearly, the Fe2 ions accessed greater concen-trations of Co, Mn and Ni than occurred where they were not employed.
! In conclusion, it should be apparent that those ~--¦ processes disclosed herein for redox leaching are highly ! 30 effective in selectively extracting useful metals such as nickel and cobalt, as well as iron and manganese, and copper ! when present, from lateritic ores and manganese ores, both terrestrial and sea nodules. Not only are these metals extracted in nearly guantitative yields but the processes operate at low temperature and pressures and without incurring the expense of costly reagents or reagents that cannot be regenerated inexpensively~

~, .

Insofar as the latter regeneration i6 considered, those processes that have been disclosed herein can be characterized by fast, clean, relatively inexpensive steps utilizing only H2, CO or syngas and without elaborate processing or producing deleterious by-products. It should also be evident that, if desired, another useful feature of the present invention is that it provides processes whereby chromium and certain precious metals, contained in the ores treated can now be extracted inasmuch as the various processes do not access these metals to any significant extent, in effect, concentrating the content in the solid ore residue from whence t~o or three times the original percentage per unit weight is provided.
Thus, it should be apparent to those skilled in the art that the ARI~ processes and those modifications and adjuncts set forth herein are operable on a variety of ore feeds, in various combinations, described or otherwise disclosed, and within various processing parameters. The present processes should not be limited by known methods of final separations of the metal ions extracted in the pregnant liquor, i.e., Fe , Mn , Ni and Co or by their point of removal and these can readily be designed into an overall system in consideration of existing equipment and/or --the by-products desired by the operator.
Furthermore, it is to be understood that all of the variables, those disclosed as well as those falling --within the existing skill in the art, fall within the scope j of the claimed invention and that the subject invention is --in no way limited by the examples and respective tables set forth herein. These have been provided merely to provide a demonstration of operability and, therefore, the selection of ores, reactants, processing steps and parameters and the like can readily be determined without departing from the spirit of the invention herein disclosed and described.
Moreover, the scope of the invention shall include all modifications and variations that fall within the scope of - the attached claims.

Claims (12)

1. A process for the extraction of ferrous, manganous and nonferrous metals from iron oxide and manganese oxide containing ores by reduction leaching comprising the steps of:
contacting the pulverized ore with a stabilized acidic cuprous ion solution cu+L in a suitable reactor at a temperature of up to about 90°C while maintaining the pH between about 1.5 and 2.5 with acid to form a slurry wherein L is a stabilizing ligand selected from the group consisting of CO, XRCN and Cl-, X being -H or -OH and R being aliphatic having from one to about four carbon atoms;
separating said slurry into a solid tailings portion and a pregnant liquor said pregnant liquor containing solubilized ferrous, manganous, cupric and other nonferrous metal ions;
selectively extracting said solubilized metal ions; and regenerating said cuprous ion solution from said solubilized cupric ions and said ligand, L in the presence of a reductant.

2. A process as set forth in Claim 1 wherein L is CO and said step of regenerating includes the steps of:
combining said solubilized cupric ions with CO and a quinolic compound selected from the group consisting of quinol, anthraquinols and naphthoqulnols at a pressure of from about O.l to about 1.5 MPa and at a temperature of from about 20° to 90°C to form an aqueous CUCO+
lixiviant and the corresponding quinonic compound;

separating said lixiviant from said quinonic compound; and regenerating said quinolic compound from said quinonic.

3. A process as set forth in Claim 1, wherein said step of regenerating includes the steps of:
dividing said cupric ion solution into first and second streams;
combining said first stream with a quinolic compound selected from the group consisting of quinol and anthraquinols to form a three phase slurry consisting essentially of free copper metal an aqueous acid phase and the corresponding quinonic compound;
separating said quinonic compound from said copper metal and aqueous acid; and combining said second stream with said copper metal and aqueous acid and with said ligand L, where L is CO or XRCN, whereby the stabilized cuprous ion solution Cu+L is formed.

4. A process, as set forth in Claim 3, wherein L is CO and said second step of combining is conducted at a pressure of from about 0.1 to about 1.5 MPa and at a temperature of from about 20° to about 90°C .

5. A process as set forth in Claim 1, wherein said step of regenerating includes the steps of:
reducing said solubilized cupric ions with syngas to form a slurry comprising copper metal, cupric ions, cuprous ions and acid; and cooling and combining said slurry with said ligand L, where L
is CO or XRCN, to form the stabilized ion solution Cu+L.

6. A process as set forth in Claim 5, wherein said step of reducing is conducted in an autoclave operating at a pressure of between about 1.5 and 5.0 MPa and at a temperature of from about 150° to 280°C.

7. A process for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions comprising the steps of:
dividing said cupric ion solution into first and second streams;
combining said first stream with a quinolic compound selected from the group consisting of quinol and anthraquinols to form a three phase slurry consisting essentially of free copper metal, an aqueous acid phase and the corresponding quinonic compound;
separating said quinonic compound from said copper metal and aqueous acid; and combining said second stream with said copper metal and aqueous acid and with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H and -OH and R is an ali-phatic radical having one to four carbon atoms, whereby the stabilized cuprous ion solution, Cu+L is formed.

8. A process for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions comprising the steps of:

reducing said solubilized cupric ions with CO to form a slurry comprising copper metal, cupric ions and acid; and cooling and combining said slurry with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H and -OH and R is an aliphatic radical having one to four carbon atoms, to form the stabilized ion solution Cu+L.

9. A process for the regeneration of stabilized cuprous ion solutions, usable as reductants, from acidic cupric ion solutions comprising the steps of:
reducing said solubilized cupric ions with syngas in an autoclave operating at a pressure of between about 1.5 and 5.0 MPa and at a temperature of from about 150° to 280°C to form a slurry comprising copper metal, cupric ions, cuprous ions and acid; and cooling and combining said slurry with a stabilizing ligand L, where L is CO or XRCN and wherein X is selected from the group consisting of -H and-OH and R is an aliphatic radical having one to four carbon atoms, to form the stabilized ion solution Cu+L.

10. A process as set forth in Claim 7, wherein L is CO and said second step of combining is conducted at a pressure of from about 0.1 to about 1.5 MPa and at a temperature of from about 20° to about 90°C.

11. A process, as set forth in Claim 8, wherein said step of reducing is conducted in an autoclave operating at a pressure of between about 1.5 and 5.0 MPa and at a temperature of from about 200° to 280°C.

12. A process, as set forth in Claim 8, including the additional step of cooling said slurry to a temperature of at least about 140°C prior to said step of combining.