CA1080979A - Method for precipitating metal cement from a solution mixed with a precipitant - Google Patents
Method for precipitating metal cement from a solution mixed with a precipitantInfo
- Publication number
- CA1080979A CA1080979A CA260,174A CA260174A CA1080979A CA 1080979 A CA1080979 A CA 1080979A CA 260174 A CA260174 A CA 260174A CA 1080979 A CA1080979 A CA 1080979A
- Authority
- CA
- Canada
- Prior art keywords
- metal
- solution
- zinc
- precipitation
- precipitant
- 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
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 59
- 239000002184 metal Substances 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 31
- 230000001376 precipitating effect Effects 0.000 title claims abstract description 16
- 239000004568 cement Substances 0.000 title 1
- 238000001556 precipitation Methods 0.000 claims abstract description 35
- 239000002245 particle Substances 0.000 claims abstract description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 44
- 239000011701 zinc Substances 0.000 claims description 38
- 229910052725 zinc Inorganic materials 0.000 claims description 34
- 230000007935 neutral effect Effects 0.000 claims description 8
- 229910052793 cadmium Inorganic materials 0.000 claims description 6
- 229910021645 metal ion Inorganic materials 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052737 gold Inorganic materials 0.000 claims description 4
- 239000010931 gold Substances 0.000 claims description 4
- 238000002386 leaching Methods 0.000 claims description 4
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 28
- 239000010949 copper Substances 0.000 abstract description 24
- 229910052802 copper Inorganic materials 0.000 abstract description 16
- 229910052742 iron Inorganic materials 0.000 abstract description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 12
- 239000002923 metal particle Substances 0.000 abstract 5
- 229910052728 basic metal Inorganic materials 0.000 description 16
- 150000003818 basic metals Chemical class 0.000 description 16
- 150000002500 ions Chemical class 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 8
- 238000009854 hydrometallurgy Methods 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000011282 treatment Methods 0.000 description 5
- 239000012535 impurity Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000003053 immunization Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 238000010310 metallurgical process Methods 0.000 description 2
- 229910000510 noble metal Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical group [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 2
- HJTAZXHBEBIQQX-UHFFFAOYSA-N 1,5-bis(chloromethyl)naphthalene Chemical compound C1=CC=C2C(CCl)=CC=CC2=C1CCl HJTAZXHBEBIQQX-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001237728 Precis Species 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- GOLCXWYRSKYTSP-UHFFFAOYSA-N arsenic trioxide Inorganic materials O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009858 zinc metallurgy Methods 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
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
- C22B15/00—Obtaining copper
- C22B15/0063—Hydrometallurgy
- C22B15/0084—Treating solutions
- C22B15/0089—Treating solutions by chemical methods
- C22B15/0091—Treating solutions by chemical methods by cementation
-
- 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
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/44—Treatment or purification of solutions, e.g. obtained by leaching by chemical processes
- C22B3/46—Treatment or purification of solutions, e.g. obtained by leaching by chemical processes by substitution, e.g. by cementation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A precipitation method is provided in which a metal is precipitated from a solution of the metal which comprises, introducing into a solution of a first metal discrete particles of metal to precipitate the first metal from the solution, and maintaining the metal particles in motion effective to re-lease precipitated metal deposited on individual portions of the metal particles; for example the metal particles may comprise non-powderous pieces of iron for precipitating copper from solution; desirably the motion if effected by subjecting the metal particles to a vibrating motion, in a vibratory reactor having a frequency and amplitude such that individual portions of metal particles are maintained in constant motion and collide with each other.
A precipitation method is provided in which a metal is precipitated from a solution of the metal which comprises, introducing into a solution of a first metal discrete particles of metal to precipitate the first metal from the solution, and maintaining the metal particles in motion effective to re-lease precipitated metal deposited on individual portions of the metal particles; for example the metal particles may comprise non-powderous pieces of iron for precipitating copper from solution; desirably the motion if effected by subjecting the metal particles to a vibrating motion, in a vibratory reactor having a frequency and amplitude such that individual portions of metal particles are maintained in constant motion and collide with each other.
Description
The invention relates to a precipitation method for precipitating metal from a solution by means of a precipitant.
In the precipitation of metal in the form of metal precipitate from a solution of the metal mixed with another metal as the precipitant, the so-called precipitation process, substantially the same processes take place regardless of the metals involved, in which an exchange of ions takes place bet-ween a noble and a base metal in the electro-chemical series.
According to the "Lexicon der H~ttentechnik" by L~ger, 4th Edition, Volume 5, Deutsche Verlagsanstalt Stuttgart, page 733, 'iprecipitation" is defined as follows (translated from the German):
"Precipitating a metal out of a solution by means of a baser metal. The baser metal has a more negative potential t~an the metal to be precipitated and releases positive ions into solution, thus charging itself negatively and discharging all cations having more positive potentials. Precipitation in ` the form of metal. The deciding factor is thus the difference -:. -in potential between the various cations under the conditions obtaining.~l Major difficulties arise in the precipitation of the widest variety of metals, in that the precipitated metal,coats the surface of the metal used as the precipitant, thus impeding, or even bringing to a halt, the electro-chemical reaction, i.e.
the exchange of ions. Other obstacles to the reaction are:
the formation of a layer of oxide upon the surface of the metal precipitant, or the formation of a coating of very small : .
gas bubbles on the surface of the metal precipitant arising from electrolytic processes.
It is the purpose of this invention to overcome these known difficulties in all types of precipitation process, and thus to produce a definite improvement not only from the economic standpoint but also from the standpoint of the yield of metal, and therefore of the efficiency of the process as a whole.
Accord.ing to the invention there is provided a method for precipitating a metal from a solution of the metal comprising introducing into a solution of a first metal a more basic metal to precipitate said first metal from said solution, 10 and - .
maintaining said more basic metal in motion effective - to release precipitated metal deposited on individual ::
portions of said more basic metal. ~.
In particular the motion of the individual portions ~
of the more basic metal is preferably maintained by carrying -out the precipitation in a vibration mill wherein the more basic metal is subj~cted to a vibratory motion having a ~re- :
quency and amplitude such that individual portions of the more ~ basic metal are maintained in constant motion and the individual : 20 portions of the more basic metal collide with each other. In ~- this way rubbing contact between the individual port~ons of the more basic metal result in remo~al of deposits of the first -~ ;
metal precipitated from the solution onto the surface of the ~ -more basic metal. -In accordance with a broad aspect of the invention, there lS provided a process for precipitating a metal from a : ; .
solution containing metal ions, said precipitating being carried . out in a vibratory reactor which contains a precipitating agent in the form of discrete particles of metal, and in which the .
solution is subjected to such frequency and amplitude that deposits on the surface of the discrete particles of metal
In the precipitation of metal in the form of metal precipitate from a solution of the metal mixed with another metal as the precipitant, the so-called precipitation process, substantially the same processes take place regardless of the metals involved, in which an exchange of ions takes place bet-ween a noble and a base metal in the electro-chemical series.
According to the "Lexicon der H~ttentechnik" by L~ger, 4th Edition, Volume 5, Deutsche Verlagsanstalt Stuttgart, page 733, 'iprecipitation" is defined as follows (translated from the German):
"Precipitating a metal out of a solution by means of a baser metal. The baser metal has a more negative potential t~an the metal to be precipitated and releases positive ions into solution, thus charging itself negatively and discharging all cations having more positive potentials. Precipitation in ` the form of metal. The deciding factor is thus the difference -:. -in potential between the various cations under the conditions obtaining.~l Major difficulties arise in the precipitation of the widest variety of metals, in that the precipitated metal,coats the surface of the metal used as the precipitant, thus impeding, or even bringing to a halt, the electro-chemical reaction, i.e.
the exchange of ions. Other obstacles to the reaction are:
the formation of a layer of oxide upon the surface of the metal precipitant, or the formation of a coating of very small : .
gas bubbles on the surface of the metal precipitant arising from electrolytic processes.
It is the purpose of this invention to overcome these known difficulties in all types of precipitation process, and thus to produce a definite improvement not only from the economic standpoint but also from the standpoint of the yield of metal, and therefore of the efficiency of the process as a whole.
Accord.ing to the invention there is provided a method for precipitating a metal from a solution of the metal comprising introducing into a solution of a first metal a more basic metal to precipitate said first metal from said solution, 10 and - .
maintaining said more basic metal in motion effective - to release precipitated metal deposited on individual ::
portions of said more basic metal. ~.
In particular the motion of the individual portions ~
of the more basic metal is preferably maintained by carrying -out the precipitation in a vibration mill wherein the more basic metal is subj~cted to a vibratory motion having a ~re- :
quency and amplitude such that individual portions of the more ~ basic metal are maintained in constant motion and the individual : 20 portions of the more basic metal collide with each other. In ~- this way rubbing contact between the individual port~ons of the more basic metal result in remo~al of deposits of the first -~ ;
metal precipitated from the solution onto the surface of the ~ -more basic metal. -In accordance with a broad aspect of the invention, there lS provided a process for precipitating a metal from a : ; .
solution containing metal ions, said precipitating being carried . out in a vibratory reactor which contains a precipitating agent in the form of discrete particles of metal, and in which the .
solution is subjected to such frequency and amplitude that deposits on the surface of the discrete particles of metal
-2- . .. .
,. " . .. ,. ~ - - -- , . . . . .
become permanently removed by movement oE the precipitated metal, characterized in that the discrete particles consist of zinc and the solution is a neutral zinc leaching solution which in addition to zinc also contains polyvalent metal ions selected from the group consisting of Cd, Co, Ni, Ag and Au and which becomes free of these metal ions by precipitation.
The ~erm more basic metal as employed in this specification is to be understood as referring to a metal higher in the electrornotive series or more negative than the first metal to be precipitated from solution. Thus iron is a more basic metal than copper and is higher than copper in the electromotive series, so that iron will precipitate copper from . :
solution.
me more basic metal employed as the precipitating agent is suitably employed in a non-powdery form, suitably in the form of large lumps, pieces, fragments or granules or even in t~e form of scraps of metal. Although the invention is not limited to particular shapes or sizes of the pieces of more basic metal, suitable pieces are found to be granules measuring from about 2 to about 10 mm.
me method of the invention permits a much more rapid precipitation than the prior art methods.
In one aspect the process of the invention can be used for the precipitation of copper from a copper solution ., .
mixed with pieces of iron, the precipitated copper deposited upon the pieces of iron being released by constant movement thereof, and being removed Erom the decopperized solution by vibrating the pieces of iron at a frequency and an amplitude such that the said pieces of iron constantly come into . - .
colli~ion with each other.
The invention can be employed in other hydro-~ ~ .
~- .
, - - , . . .
. . . .
.
7~
metallurgical processes for precipitating any metals in metal form from solutions thereof using a more basic, electro-chemically more negative metal, the more basic metal being employed in the form of pieces of metal as the precipitant.
According to one advantageous embodiment, the inven~
tion is employed in zinc hydrometallurgy for the precipitation oE metals nobler than zinc, for example Cu, Cd, Co, Ni, as metal precipitates, from a zinc solution containing these metals which is mixed with pieces of metallic zinc as the precipitant.
In another advantageous embodiment, the invention is employed in noble-metal hydrometallurgy, for example for pre-cipitating silver or gold, as metal precipitates, from cyanide solutions thereof using mixes pieces of zinc as the precipitant.
In this different embodiment it is desirable to use a vibration mill as the precipitation reactor.
The invention, together with the technological and economical advantages attainable therewith, as compared with ~ . - .
existing processes, will be explained in greater detail, in -- conjunction with a representative example from zinc hydro-metallurgy.
In zinc hydrometallurgy it has hitherto be~n customary ; to remove foreign metals, such as Cu, Cd, Co and Ni, from the neutral liquors produced, by adding to the liquors, in agitators, metallic zinc powder and thus precipitating-out the said impu-rities.
; This known method, however, has the particular dis-`~ advantage, among others, that the zinc powder first of all has to be produced, for example by spraying metallic zinc. Further-more, the reaction between the precipitant powder and the liquor is extremely slow and may take several hours, because an immunizing layer of zinc oxide forms upon the particles of _~_ . :
.: . . , , . :
- :, ,'',',", ' '' ' '' . . ~ .: ' ' '. ''':'' .: ' , : . , : :: . . .
zinc, and this layer definitely inhibits the course of the reaction.
In contrast to this prior method, the invention makes use of larger non-powderous pieces of zinc instead of zinc powder, the zinc may for example be added to the liquor in the form of granules measuring from 2 and 10 mm, the entire precipitation process can be conclucted using a vibration mill as the precipitation reactor, in order to produce the intensive vibration required to cause the zinc granules to come into - 10 collision with each other.
In the method of the invention, this intensive vi-bration of the pieces o~ the zinc, which can be achieved simply and economically in a vibration mill, causes the surfaces of the pieces of zinc coated with the precipitated nobler metal to ~ -, . . .
; constantly collide with each other and to be rubbed bare, with the result that the activity of the surfaces of the zinc are maintained, so that the reaction by the exchange of ions con-tinues.
The intenqive vibration of the precipitation reactor containing the pieces of metal also produces intense tur~ulence in the liquor, and this brings about a thorough mixing of the solid and liquid phases in the boundary layer between the li-quid and the pieces of more basic metal. As a result of this, . ,~, ~
the ion concentration in the vicinity of the surface of the m~re basic metal precipitant is substantially higher than it is in conventional precipitation methods, and this speeds up still ~ `
further the transfer of material. Moreover, the hydrogen gas - -released by the reaction into the liquor is in the form of very small bubbles, and this considerably reduces its effect as a reducing agent.
In æinc hydrometallurgy, for example, the invention . . :, : . .. . .. , . ~ . . .. ... . ...
improves the economics of the process by replacing expensive zinc powder, used as the precipitant, by inexpensive zinc waste and intermediate products, for example as dross and slag from metallurgical processes. Some of the dross produced during the smelting and casting of zinc cathodes made by electrolysis consists only partly of metallic zinc~ Dross of this kind has to be refined by segregating the zinc, the residue being returned to the zinc-leaching operation where it is dissolved.
All of this costly processing becomes redundant and may be eliminated if, according to the teaching of the inven-tion, precipitation is carried out, not with zinc powder, but with dross, waste, granular or lump metallic zinc in a vibrat-~ ing container such as a precipitation reactor, since the ~-; energy produced by the precipitation reactor imparts to the content thereof a high energy potential such that the pieces - of zinc constantly knock and rub violently against each other.
e surfaces thereof are thus kept free of contaminants or immunizing coatings, be they in the form of oxides, deposits of metal precipitate, or collections of gas bubbles. mis :
results in an accelerated transfer of material produced by the .
exchange of ions between the metal and the solution.
The final result of this is a considerable reduction in the duration of the process and a better utilization of the metallic substances used, the consumption thereof being reduced a~most to the stoichiometric value, whereas in conventional precipitation drums, this consumption may amount to up to 500% ;
of the stoichiometric value.
m e technological and economic advantages and possi-I bilities demonstrated in the foregoing example taXen from zinc - 30 metallurgy also apply to other applications of the principle of the invention, in practically all precipitation processes in .~ .
. , ~
.
-6- ~
~. - . . .
. . " .. -.. .
the field of hydrometallurgy.
The invention is explained hereinafter in greater de-tail, in conjunction with two examples of precipitation according to the prior art and two examples of precipitation processes according to the invention.
EXAMPLE_I
Precipitation ~rocess according_to the prl r art:
A liquor was provided containing, in solution, metal compounds obtained by chlorinating the volatilization product from a complex iron ore the metal compounds having the follow-., ing metal contents 25 g/1 Cu, 3 g/l Fe; 80 g/l zinc, l g/l Pbremainder Bi, Co, Cd, Ag about 200 mg/l.
About 30 m3 of the liquor, containing the dissolved metals, is loaded into a precipitation drum having a capacity of about lO0 m3, the drum being pear-shaped and set at an angle for rotation about its axis, and having an acid-resistant lining. About 50 t of Fe scrap is introduced into the drum through a top opening. The load is moved for about 120 minutes at a temperature of 50C by rotating the drum.
m e final liquor contains about 380 mg/l of Cu.
The scrap consumed in this batch process was about 215% of the stoichiometric amount of Fe.
TEXAMPLE II
Canventional preci~itation:
In zinc metallurgy, neutral leaching produces a neutral liquor which contains, in addition to the dissolved zinc oxides, various amounts of dissolved ions of electro-chemically more noble metals, mainly Cu, Ni, Co and Cd~
.;
These foreign metals which, as compared with the zinc metal to be recovered, are to be regarded as impurities, must , . ..... ..
~, . .
, . . -, : ~, , "
' - ' ' , . ' ': ~. - . . ~ , , .:
be precipitated out of the liquor, since even small quantities thereof would have an extremely detrimental effect upon the subsequent electrolysis of the zinc.
These metallic impurities are precipitated with zinc dust, since the said impurities are electro-chemically more positive than the zinc.
Precipitation is carried out intermittently in a stirring kettle, the zinc dust being added batch-wise. The liquor introduced contains: 150 g/l Zn; 500 mg/l Cu:
- 10 400 mg/l Cd; 20 mg/l Ni; and 20 mg/l Co. ;
The liquor is subjected to the precipitation process 5 in the first stage at 95C, with additions of Zn dust, CUSO4 ~ ;
" and arsenic trioxide, the Cu, Co, Ni and As precipitate out a precipitate, whereas the Cd remains in solution.
The period of residence in each precipitation stage is l about 260 minutes. The consumption~of Zn dust is 530% of the -, theoretical, stoichiometric amount of Zn.
' The purified neutral liquor contains as residual im- ;
;
~ purities:Cu 0.1 mg/l; Co 0.2 mg/l; Ni 0.05 mg/l; Cd 0.2 . :
` 20 mg/l.
EXAMPLE III
Precip t tion acc_rdinq to the invention:
` The copper solution of a neutral liquox of oxidic -~i copper-ore concentrate is precipitated, using scrap iron as .~
t~e precipitant. The precipitation process is carried out in a test set-up with the aid of a vibrating mill, the r.p.m.
and amplitude of which are adjustable. The reactor is a heat-:j , able satellite rigidly attached to the said vibrating mill and having a capacity of 8.5 dm3. The charge of scrap iron pre-cipitating agent is 65% of the volume of the reactor, i~e. 5.5 dm3. The amount of liquor is 45% of the volume of the reactor, :~ , .
~ ~ 8 ~-., .
:: . ~ , . ,,: . .
:: . , : , . ~ , : .
i.e. 3 dm3.
Precipitation of the copper from the CuS04 solution with scrap iron starts at a Cu content of 36 g/l. The amplitu-de is 10 mm, the frequency of vibration 12.5 Hz. The treat-ment temperature is 18C. The treatment time 180 seconds.
A residual Cu content of 40 mg/l Cu is found by ana-lysis.
A parallel test carried out under strictly similar conditions, but at a treatment temperature of 63C produces a residual Cu content of 40 mg/l after only 32 seconds.
In both cases the scrap-iron consumption corresponds to 1.2 times the stoichiometric amount of iron.
EX~MPLE IV
Precipitation accordinq to the invention The precipitation of copper with granular zinc from a ~;~
neutral zinc liquor is carried out in the same test reactor on the vibrating mill.
`~ With 150 g/l of zinc, the content of dissolved copper at the start of the reaction amounts to about 500 mg/l.
Treatment temperature 95 C. pH value of the liquor 4.
The granular zinc used as the precipitant lies within the 3 to 10 mm grain ~ixe. The treatment is carried out with vibration at an amplitude of 10 mm and a frequency of 12.5 Hz.
~After a precipitating period of 32 seconds, analysis .:
r~vealed a final copper content of less than 0.1 mg/l.
Applications of the principle of the method to other - precipitation processes in the field of hydrometallurgy lie - :.
within the scope of the invention.
; ':
~9~ :
,. " . .. ,. ~ - - -- , . . . . .
become permanently removed by movement oE the precipitated metal, characterized in that the discrete particles consist of zinc and the solution is a neutral zinc leaching solution which in addition to zinc also contains polyvalent metal ions selected from the group consisting of Cd, Co, Ni, Ag and Au and which becomes free of these metal ions by precipitation.
The ~erm more basic metal as employed in this specification is to be understood as referring to a metal higher in the electrornotive series or more negative than the first metal to be precipitated from solution. Thus iron is a more basic metal than copper and is higher than copper in the electromotive series, so that iron will precipitate copper from . :
solution.
me more basic metal employed as the precipitating agent is suitably employed in a non-powdery form, suitably in the form of large lumps, pieces, fragments or granules or even in t~e form of scraps of metal. Although the invention is not limited to particular shapes or sizes of the pieces of more basic metal, suitable pieces are found to be granules measuring from about 2 to about 10 mm.
me method of the invention permits a much more rapid precipitation than the prior art methods.
In one aspect the process of the invention can be used for the precipitation of copper from a copper solution ., .
mixed with pieces of iron, the precipitated copper deposited upon the pieces of iron being released by constant movement thereof, and being removed Erom the decopperized solution by vibrating the pieces of iron at a frequency and an amplitude such that the said pieces of iron constantly come into . - .
colli~ion with each other.
The invention can be employed in other hydro-~ ~ .
~- .
, - - , . . .
. . . .
.
7~
metallurgical processes for precipitating any metals in metal form from solutions thereof using a more basic, electro-chemically more negative metal, the more basic metal being employed in the form of pieces of metal as the precipitant.
According to one advantageous embodiment, the inven~
tion is employed in zinc hydrometallurgy for the precipitation oE metals nobler than zinc, for example Cu, Cd, Co, Ni, as metal precipitates, from a zinc solution containing these metals which is mixed with pieces of metallic zinc as the precipitant.
In another advantageous embodiment, the invention is employed in noble-metal hydrometallurgy, for example for pre-cipitating silver or gold, as metal precipitates, from cyanide solutions thereof using mixes pieces of zinc as the precipitant.
In this different embodiment it is desirable to use a vibration mill as the precipitation reactor.
The invention, together with the technological and economical advantages attainable therewith, as compared with ~ . - .
existing processes, will be explained in greater detail, in -- conjunction with a representative example from zinc hydro-metallurgy.
In zinc hydrometallurgy it has hitherto be~n customary ; to remove foreign metals, such as Cu, Cd, Co and Ni, from the neutral liquors produced, by adding to the liquors, in agitators, metallic zinc powder and thus precipitating-out the said impu-rities.
; This known method, however, has the particular dis-`~ advantage, among others, that the zinc powder first of all has to be produced, for example by spraying metallic zinc. Further-more, the reaction between the precipitant powder and the liquor is extremely slow and may take several hours, because an immunizing layer of zinc oxide forms upon the particles of _~_ . :
.: . . , , . :
- :, ,'',',", ' '' ' '' . . ~ .: ' ' '. ''':'' .: ' , : . , : :: . . .
zinc, and this layer definitely inhibits the course of the reaction.
In contrast to this prior method, the invention makes use of larger non-powderous pieces of zinc instead of zinc powder, the zinc may for example be added to the liquor in the form of granules measuring from 2 and 10 mm, the entire precipitation process can be conclucted using a vibration mill as the precipitation reactor, in order to produce the intensive vibration required to cause the zinc granules to come into - 10 collision with each other.
In the method of the invention, this intensive vi-bration of the pieces o~ the zinc, which can be achieved simply and economically in a vibration mill, causes the surfaces of the pieces of zinc coated with the precipitated nobler metal to ~ -, . . .
; constantly collide with each other and to be rubbed bare, with the result that the activity of the surfaces of the zinc are maintained, so that the reaction by the exchange of ions con-tinues.
The intenqive vibration of the precipitation reactor containing the pieces of metal also produces intense tur~ulence in the liquor, and this brings about a thorough mixing of the solid and liquid phases in the boundary layer between the li-quid and the pieces of more basic metal. As a result of this, . ,~, ~
the ion concentration in the vicinity of the surface of the m~re basic metal precipitant is substantially higher than it is in conventional precipitation methods, and this speeds up still ~ `
further the transfer of material. Moreover, the hydrogen gas - -released by the reaction into the liquor is in the form of very small bubbles, and this considerably reduces its effect as a reducing agent.
In æinc hydrometallurgy, for example, the invention . . :, : . .. . .. , . ~ . . .. ... . ...
improves the economics of the process by replacing expensive zinc powder, used as the precipitant, by inexpensive zinc waste and intermediate products, for example as dross and slag from metallurgical processes. Some of the dross produced during the smelting and casting of zinc cathodes made by electrolysis consists only partly of metallic zinc~ Dross of this kind has to be refined by segregating the zinc, the residue being returned to the zinc-leaching operation where it is dissolved.
All of this costly processing becomes redundant and may be eliminated if, according to the teaching of the inven-tion, precipitation is carried out, not with zinc powder, but with dross, waste, granular or lump metallic zinc in a vibrat-~ ing container such as a precipitation reactor, since the ~-; energy produced by the precipitation reactor imparts to the content thereof a high energy potential such that the pieces - of zinc constantly knock and rub violently against each other.
e surfaces thereof are thus kept free of contaminants or immunizing coatings, be they in the form of oxides, deposits of metal precipitate, or collections of gas bubbles. mis :
results in an accelerated transfer of material produced by the .
exchange of ions between the metal and the solution.
The final result of this is a considerable reduction in the duration of the process and a better utilization of the metallic substances used, the consumption thereof being reduced a~most to the stoichiometric value, whereas in conventional precipitation drums, this consumption may amount to up to 500% ;
of the stoichiometric value.
m e technological and economic advantages and possi-I bilities demonstrated in the foregoing example taXen from zinc - 30 metallurgy also apply to other applications of the principle of the invention, in practically all precipitation processes in .~ .
. , ~
.
-6- ~
~. - . . .
. . " .. -.. .
the field of hydrometallurgy.
The invention is explained hereinafter in greater de-tail, in conjunction with two examples of precipitation according to the prior art and two examples of precipitation processes according to the invention.
EXAMPLE_I
Precipitation ~rocess according_to the prl r art:
A liquor was provided containing, in solution, metal compounds obtained by chlorinating the volatilization product from a complex iron ore the metal compounds having the follow-., ing metal contents 25 g/1 Cu, 3 g/l Fe; 80 g/l zinc, l g/l Pbremainder Bi, Co, Cd, Ag about 200 mg/l.
About 30 m3 of the liquor, containing the dissolved metals, is loaded into a precipitation drum having a capacity of about lO0 m3, the drum being pear-shaped and set at an angle for rotation about its axis, and having an acid-resistant lining. About 50 t of Fe scrap is introduced into the drum through a top opening. The load is moved for about 120 minutes at a temperature of 50C by rotating the drum.
m e final liquor contains about 380 mg/l of Cu.
The scrap consumed in this batch process was about 215% of the stoichiometric amount of Fe.
TEXAMPLE II
Canventional preci~itation:
In zinc metallurgy, neutral leaching produces a neutral liquor which contains, in addition to the dissolved zinc oxides, various amounts of dissolved ions of electro-chemically more noble metals, mainly Cu, Ni, Co and Cd~
.;
These foreign metals which, as compared with the zinc metal to be recovered, are to be regarded as impurities, must , . ..... ..
~, . .
, . . -, : ~, , "
' - ' ' , . ' ': ~. - . . ~ , , .:
be precipitated out of the liquor, since even small quantities thereof would have an extremely detrimental effect upon the subsequent electrolysis of the zinc.
These metallic impurities are precipitated with zinc dust, since the said impurities are electro-chemically more positive than the zinc.
Precipitation is carried out intermittently in a stirring kettle, the zinc dust being added batch-wise. The liquor introduced contains: 150 g/l Zn; 500 mg/l Cu:
- 10 400 mg/l Cd; 20 mg/l Ni; and 20 mg/l Co. ;
The liquor is subjected to the precipitation process 5 in the first stage at 95C, with additions of Zn dust, CUSO4 ~ ;
" and arsenic trioxide, the Cu, Co, Ni and As precipitate out a precipitate, whereas the Cd remains in solution.
The period of residence in each precipitation stage is l about 260 minutes. The consumption~of Zn dust is 530% of the -, theoretical, stoichiometric amount of Zn.
' The purified neutral liquor contains as residual im- ;
;
~ purities:Cu 0.1 mg/l; Co 0.2 mg/l; Ni 0.05 mg/l; Cd 0.2 . :
` 20 mg/l.
EXAMPLE III
Precip t tion acc_rdinq to the invention:
` The copper solution of a neutral liquox of oxidic -~i copper-ore concentrate is precipitated, using scrap iron as .~
t~e precipitant. The precipitation process is carried out in a test set-up with the aid of a vibrating mill, the r.p.m.
and amplitude of which are adjustable. The reactor is a heat-:j , able satellite rigidly attached to the said vibrating mill and having a capacity of 8.5 dm3. The charge of scrap iron pre-cipitating agent is 65% of the volume of the reactor, i~e. 5.5 dm3. The amount of liquor is 45% of the volume of the reactor, :~ , .
~ ~ 8 ~-., .
:: . ~ , . ,,: . .
:: . , : , . ~ , : .
i.e. 3 dm3.
Precipitation of the copper from the CuS04 solution with scrap iron starts at a Cu content of 36 g/l. The amplitu-de is 10 mm, the frequency of vibration 12.5 Hz. The treat-ment temperature is 18C. The treatment time 180 seconds.
A residual Cu content of 40 mg/l Cu is found by ana-lysis.
A parallel test carried out under strictly similar conditions, but at a treatment temperature of 63C produces a residual Cu content of 40 mg/l after only 32 seconds.
In both cases the scrap-iron consumption corresponds to 1.2 times the stoichiometric amount of iron.
EX~MPLE IV
Precipitation accordinq to the invention The precipitation of copper with granular zinc from a ~;~
neutral zinc liquor is carried out in the same test reactor on the vibrating mill.
`~ With 150 g/l of zinc, the content of dissolved copper at the start of the reaction amounts to about 500 mg/l.
Treatment temperature 95 C. pH value of the liquor 4.
The granular zinc used as the precipitant lies within the 3 to 10 mm grain ~ixe. The treatment is carried out with vibration at an amplitude of 10 mm and a frequency of 12.5 Hz.
~After a precipitating period of 32 seconds, analysis .:
r~vealed a final copper content of less than 0.1 mg/l.
Applications of the principle of the method to other - precipitation processes in the field of hydrometallurgy lie - :.
within the scope of the invention.
; ':
~9~ :
Claims (4)
1. Process for precipitating a metal from a solution containing metal ions, said precipitating being carried out in a vibratory reactor which contains a precipitating agent in the form of discrete particles of metal, and in which the solution is subjected to such frequency and amplitude that deposits on the surface of the discrete particles of metal become permanently removed by movement of the precipitated metal, characterized in that the discrete particles consist of zinc and the solution is a neutral zinc leaching solution which in addition to zinc also contains polyvalent metal ions selected from the group consisting of Cd, Co, Ni, Ag and Au and which becomes free of these metal ions by precipitation.
2. A process according to claim 1, wherein the discrete particles have a dimension of from about 2 to about 10 mm.
3. A process according to claim 2, wherein said frequency is about 12.5 Hz and said amplitude is about 10 mm.
4. A process according to claim 1, 2 or 3 wherein said solution is a cyanide solution of at least one metal selected from the group consisting of gold and silver and said discrete particles consist of zinc.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2540100A DE2540100C2 (en) | 1975-09-09 | 1975-09-09 | Use of a device for the continuous precipitation of cement copper from a copper solution mixed with pieces of iron |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1080979A true CA1080979A (en) | 1980-07-08 |
Family
ID=5955969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA260,174A Expired CA1080979A (en) | 1975-09-09 | 1976-08-30 | Method for precipitating metal cement from a solution mixed with a precipitant |
Country Status (13)
Country | Link |
---|---|
JP (1) | JPS5233802A (en) |
BE (1) | BE845761A (en) |
CA (1) | CA1080979A (en) |
DE (1) | DE2540100C2 (en) |
ES (1) | ES451241A2 (en) |
FI (1) | FI66911C (en) |
FR (1) | FR2323768A1 (en) |
GB (1) | GB1562705A (en) |
IT (1) | IT1069264B (en) |
NL (1) | NL7610036A (en) |
NO (1) | NO763073L (en) |
ZA (1) | ZA765396B (en) |
ZM (1) | ZM11276A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2007039788A (en) * | 2005-07-06 | 2007-02-15 | Kobelco Eco-Solutions Co Ltd | Process for recovery of metals and equipment therefor |
JP6205290B2 (en) * | 2014-02-14 | 2017-09-27 | 田中貴金属工業株式会社 | Method for recovering gold or silver from cyanic waste liquid containing gold or silver |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD64891A (en) * | ||||
GB518981A (en) * | 1938-09-12 | 1940-03-13 | Wilfred William Groves | A method for treating materials of different phases and apparatus therefor |
US3511488A (en) * | 1966-09-29 | 1970-05-12 | Robert Arthur Stubblefield | Ultrasonic copper precipitator |
BE789907A (en) * | 1971-10-27 | 1973-02-01 | Compania De | CEMENTATION PROCESS |
CH556391A (en) * | 1972-06-30 | 1974-11-29 | Pertusola Soc Mineraria | PROCEDURE AND APPARATUS FOR PURIFYING A ZINCIFIER SOLUTION, INTENDED IN PARTICULAR FOR THE ELECTROLYTIC PREPARATION OF ZINC. |
-
1975
- 1975-09-09 DE DE2540100A patent/DE2540100C2/en not_active Expired
-
1976
- 1976-08-24 GB GB35224/76A patent/GB1562705A/en not_active Expired
- 1976-08-27 ZM ZM112/76A patent/ZM11276A1/en unknown
- 1976-08-30 CA CA260,174A patent/CA1080979A/en not_active Expired
- 1976-09-01 BE BE170283A patent/BE845761A/en not_active IP Right Cessation
- 1976-09-03 ES ES451241A patent/ES451241A2/en not_active Expired
- 1976-09-06 FI FI762544A patent/FI66911C/en not_active IP Right Cessation
- 1976-09-07 FR FR7626846A patent/FR2323768A1/en not_active Withdrawn
- 1976-09-07 IT IT51156/76A patent/IT1069264B/en active
- 1976-09-08 NO NO763073A patent/NO763073L/no unknown
- 1976-09-09 ZA ZA765396A patent/ZA765396B/en unknown
- 1976-09-09 NL NL7610036A patent/NL7610036A/en not_active Application Discontinuation
- 1976-09-09 JP JP51107334A patent/JPS5233802A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE2540100C2 (en) | 1982-10-28 |
NL7610036A (en) | 1977-03-11 |
FI66911C (en) | 1984-12-10 |
ZA765396B (en) | 1977-08-31 |
NO763073L (en) | 1977-03-10 |
FI762544A (en) | 1977-03-10 |
ES451241A2 (en) | 1978-01-16 |
JPS5233802A (en) | 1977-03-15 |
DE2540100A1 (en) | 1977-03-17 |
GB1562705A (en) | 1980-03-12 |
IT1069264B (en) | 1985-03-25 |
FI66911B (en) | 1984-08-31 |
BE845761A (en) | 1976-12-31 |
FR2323768A1 (en) | 1977-04-08 |
ZM11276A1 (en) | 1977-07-21 |
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