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I S S U E 8 A P R I L 2 0 0 3
acorganotesacorga notes
Metal Extract ion Products
(pages 4-6)
Compañía
MineraDisputada DeLas Condespages 2-3
Manufacturing
Qualitypages 7-8
Organizational
Newspage 8
Solvent Extraction of Copperfrom High Concentration
Pressure Acid Leach Liquors
Fifth Annual
TechnicalACORGASeminar inChilepage 9
Aqueous Con-
tinuous: Flexibilityto MaintainProduction withFalling PLS CuGradepages 10-11
Upcoming
Industry Eventspage 12
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Compañía Minera Disputada DeLas Condes: A New SX/EW Plant
At The San Francisco DepositGonzal o Al varez Brantes, Techni cal Manager, Avecia Chi le Ltda., Sant iago
Compañía Minera Disputada de
Las Condes harvested its first cathode
on February 27, 2002. This new
Solvent Extraction and Electrowinning
(SX/EW) plant is located only 65 km
Northeast of Santiago, at an altitude of
2,750 meters, and is fed by leaching
the low grade ore from the San
Francisco deposit. With this new plant
Minera Disputada adds 20,000 metrictons/year of cathode production to
the 5,200 tons/year produced by
the El Soldado property and the
11,900 tons/year produced by the
Los Bronces property.
The project feasibility studies
were completed in late 1999 and
engineering and construction began
in early 2000. Engineering design
work was completed by Ingeniería
SX, a group formed by the companies
Bechtel and ARA. Vial and Vives
Construction completed the project
construction work.
The Los Bronces Mine is expected
to generate a total of 1,200 million
metric tons of material from the San
Francisco deposit. Approximately 60%
of the total ore will be leached (720
million tons of low-grade ore at 0.2-
0.7% Cu). Mining is planned for a 25-
year period. Leaching design will pro-
vide 200,000 m3 of area for leaching.
Both the solvent extraction and
the electrowinning plants are unique
from the construction point of view
because they are located in the old Mill
and Concentrator buildings. These
structures have not been in operation
since 1992. The use of the existing
buildings provided a savings of $2.5
million dollars on the construction
project. The location of the SX/EW
processes in the enclosed facilities
also provides protection from the
2
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snow during the winter, when operations take place at tem-
peratures well below zero degrees Celsius. A traditional tank
farm is not seen at the Los Bronces plant.
The solvent extraction plant was designed withtwo stages of extraction and one stage of stripping using
traditional mixer settlers. The mixers consist of a primary
pump mixer, with two auxiliary mixers for extraction
stages and one auxiliary mixer for the stripping stage (all
stainless steel). Coalescers are used to reduce any aqueous
entrainment in the loaded organic. Flexibility was included
in the design to allow PLS flows to be fed as either: one
stream, processed through the two extract stages in series;
or, two separate PLS streams to each extract stage, processed
in parallel. Seven 1,000 HP impulsion pumps take the
raffinate up to the leaching area.
The Electrowinning plant, located in the same building,
operates with stainless steel starter sheets and has 66 cells.
Current density is 330 A/m2. To minimize the acid mist in
the tankhouse, Minera Disputada helped develop a system
to capture the acid mist from the EW operation. The SAME
system consists of a hood located over each electrolyte cell.
The hood collects the mist and processes it in a countercur-
rent scrubber with a water shower. The captured acid fromthe mist is then returned to the process.
The start up of the new plant was very smooth.
Several factors contributed to this success. Site staff was
hired early during the engineering and construction stages,
and personnel were selected who had significant experience
in plant operation. This approach allowed members of the
team to be incorporated in the project at the appropriate
time and, at the same time, allowed their participation
in appropriate training courses. One such example was
the SX/EW course given by the members of the Avecia
Santiago office. Minera Disputada’s approach and the
training received by the workers were significantcontributions to the successful start-up of the plant.
waste dump
1150 m3/ hr flow in series operation
(2645 m3/ hr flow in parallel operation)
2.27 gpl Cu; 1.8 – 3.0 pH; 3.6 gpl Fe+++; 42.7 gpl SO4—;
200 mg/ l Cl-; 438 mg/ l Mn; 4.37 gpl Al.
3 - 5.5 °C
90%
1156 m3
/ hr flow~9.0 v/o ACORGA® PT- 5050MD
Escaid 110; 0.5 % of aromatic diluent
2E + 1S (with flexibility to operate as 1E + 1E + 1S)
38 gpl Cu; 156.4 gpl H+; 0.6 gpl Fe+++; 18 mg/ l Cl-;
20 mg/l Mn; 140 mg/ l Co++ at 41 - 49 °C.
1112.5 m3/ hr flow
66
60
61
140 l/ hr per m2
276 - 370 A/ m2
92 %
OPERATIONAL PARAMETERS
Leaching:
PLS:
PLS Temperature:
Recovery Target:
Organic:
Configuration:
Lean Electrolyte:
Lean Electrolyte to Cells:
Number of cells:
Cathodes per cell:
Anodes per cell:
Specific flow to cells:
Current density:
Current efficiency:
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4
THE KONKOLA DEEPS EXPANSION PROJECT
Solvent Extraction of Copperfrom High Concentration
Pressure Acid Leach Liquors
Kathryn C. Sole, Anglo American Research Laboratori es (Pty) Ltd, Johannesburg, South Af ri ca
The Konkola Deeps sulphide
deposit in Zambia occurs in the
immediate vicinity of a large surface
oxide deposit known as the Chingola
refractory ore (CRO), as well as sometwo decades’ worth of accumulated
oxide tailings material from the
adjacent Nchanga Tail ings Leach Plant.
Both oxides contain economically
attractive quantities of copper (~1%).
As part of an assessment of various
scenarios associated with the expansion
of the underground mine, a hydromet-
allurgical process route for the
treatment of both the sulphide and
oxide materials was evaluated.
Process Conc ept
In the proposed hydrometallurgical
flow sheet (Figure 1), the sulphide
material was concentrated by flotation
to 40-45% Cu and then subjected to a
high pressure acid leach (HPAL) under
conditions that maximized recovery of
copper and cobalt while rejecting iron
as hematite. The autoclave discharge
contained 60 g/l Cu and 5 g/l H2SO4.
This enabled the pregnant leach
solution (PLS1) to be purified directly
by SX without neutralization. The high
tenor SX1 circuit removed the bulk
of the copper, the extraction of
50 g/l Cu generating a raffinate stream
that contained about 80 g/l H2SO4.
This acid was then used to leach
copper from the CRO. The aggressive
leaching conditions were necessitated
by the substantial amounts of
aluminum, magnesium, and calcium
oxides and carbonates in this material
that consume acid in leaching and
effectively act as an ‘acid sink’. Copper
was recovered from the atmospheric
leach liquor in the low tenor SX2
circuit. Both SX circuits were integrat-
ed with electrowinning to produce a
high-grade copper cathode product.
This flow sheet capitalized on the
synergy that exists between the leach-
ing of the sulphide copper concentrate
(acid producing) and the oxide copper
ore (acid consuming). Copper leachedin the autoclave provided a convenient
way of ‘transferring acid’ from the sul-
phide circuit to the oxide circuit. Key
to the concept was the specification of
a copper SX circuit operating at a high
extraction efficiency of copper (∆Cu =
50 g/l), thereby providing a raffinate
solution of sufficient acid strength to
successfully leach the refractory CRO
minerals. The high tenor SX circuit
(SX1) focused on maximizing the
copper extraction using a high
extractant concentration and a high
flow rate of the organic phase relative
to the aqueous phase (O:A). The low
tenor circuit (SX2) was responsible for
generating a raffinate as low in copper
as possible (<0.5 g/l).
Pilot-Plant Evaluation
The integrated flow sheet waspiloted at AARL during 2000, produc-
ing 24 kg/h cathode copper. The eight-
week campaign treated 27 tons of CRO
and 2.5 tons of Konkola concentrate,
and produced 940 kg of LME A Grade
copper cathode [1, 2].
The HPAL achieved high extrac-
tions of both copper (98.1%) and
cobalt (96.5%) from the concentrate.
The acid tenor of the autoclave dis-
charge liquor averaged 6.5 g/l.
O/ F
O/ FU/ F
Raffinate
Konkola concentrate
U/ F
CRO ore
ResidueCopper cathode
High tenor SX
Thickener
High pressureacid leach
Second-stageatmospheric leach
Thickener
Filtration
CCDLow tenor SX
Copper EW
First-stageatmospheric leach
Figure 1: The hydrom etallurgical flow sheet for the Konko la project.
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Figure 2: SX1 solvent-extraction circuit used in the Konkola pilot cam paign.
Although slightly higher than the target value of 5 g/l, this
was still low enough to allow the liquor to be fed directly to
the SX1 circuit. Copper extraction from the CRO material
averaged 77.5%. The acid concentration of the atmospheric
leach liquor was 2.7 g/l. Two extractants were tested during
the campaign. The Avecia extractant tested was ACORGA®
M-5640. The diluent was Shellsol 2325. The operating con-
ditions for the two SX circuits are shown in Table I.
Parameter
Extractant concentration (vol. % )Temperature (ºC)Mixer volume (l)
Settling area (m2
)
32407. 5
0.15
Clarified autoclave d ischarge60 g/ l Cu, 4.2 g/l H2SO 4
4. 950
0. 937 g/ l Cu, 170 g/ l H2SO 4
46 g/ l Cu, 156 g/ l H2SO 4
164012
0.22
Clarified CRO leach liquor5.3 g/ l Cu, 1.6 g/ l H2SO 4
1. 04. 8
1. 837 g/ l Cu, 170 g/ l H2SO 4
45 g/ l Cu, 157 g/ l H2SO 4
Extraction circuitPLSPLS compositionAdvance O: ATarget ∆Cu (g/l)
Strip circuitAdvance O:AStrip liquor (SE)Loaded strip liquor ( AE)
SX1 SX2
Table I: Konkola pilot-plant operating cond itions for the SX circuits.
The SX1 circuit consistentlyobtained the required copper extrac-
tion of 50 g/l. The performance of
the SX2 circuit also exceeded the
specifications; with average raffinate
tenors of 0.25 g/l Cu - well below the
target value of 0.5 g/l. Typical solution
analyses obtained during the campaign
are given in Table II. Although normal
crud formation occurred, no adverse
physical effects on the organic phase
were observed.
Electrowinning of copperfrom the loaded strip liquor
consistently produced LME A Grade
throughout the campaign, with all
cathodes meeting the BSI standard BS
6017:1981 with respect to individual
element impurities.
SX1
CuCoFeAl
MgCaMnZn
59.291.231.221.127.950.651.310.10
15.6< 0.001< 0.001< 0.001< 0.001< 0.001< 0.001
0.001
6.2< 0.001< 0.001< 0.001< 0.001
0.001< 0.001< 0.001
PLS
5.810.611.771.316.830.691.220.05
8.85< 0.001< 0.001< 0.001< 0.001< 0.001< 0.001< 0.001
3.8< 0.001< 0.001< 0.001< 0.001< 0.001< 0.001
0.001
LO SO
Element(g/ l)
SX2
PLS LO SO
Table II: Typical perform ance of SX1 and SX2 circuits during the Konkola piloting cam paign.
“Th e su ccessfu l compl et ion of t he Konkola pi lot plant d em onstr at ed tha t exi st in g ext racta nt s can be used in t hi s
non-trad i t ional appl icat ion wit hout problem s.”
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6
CONCLUSIONS
Pressure leaching technologies currently under
development for the treatment of copper sulphide concen-
trates yield leach liquors that can contain in excess of 50 g/l
Cu. The purification of such liquors by SX requires an
integrated flow sheet in which the large quantities of acidproduced by the extraction reaction can be accommodated.
This work demonstrated that extractant concentrations up
to 32 vol.% can achieve copper transfers of >50 g/l in three
stages. Adequate stripping is achieved in two stages with
a conventional composition of the spent electrolytes, and
producing an advance electrolyte from which LME A Grade
copper cathode can be electrowon.
The performance of conventional SX extractants and
circuit configurations for transferring such high amounts of
copper without neutralization had not been documented
previously for continuous trials. The successful completion of
the Konkola pilot plant demonstrated that existing
extractants can be used in this non-traditional application
without problems.
ACKNOWLEDGMENTS
This article is published courtesy of Anglo American
Research Laboratories (Pty) Ltd.
NOTE
This work was carried out in 2000, during whichtime Konkola Copper Mines was jointly owned by Zambian
Consolidated Copper Mines (ZCCM) and Zambian Copper
Investments (ZCI), of which Anglo American plc was the
major shareholder. Anglo American currently holds no
financial interest in KCM.
REFERENCES
1.Whyte, R. M., Schoeman, N., and Bowes, K. G. (2001),
Processing of Konkola copper concentrates and Chingola
refractory ore in a fully integrated hydrometallurgical
pilot plant circuit. Copper, Cobalt, Nickel and Zinc
Recover, South African Institute of Mining and
Metallurgy, Johannesburg, 15 pp.
2.Sole, K. C. (2002), Solvent extraction of copper from
high concentration pressure acid leach liquors,
Proceedings International Solvent Extraction
Conference ISEC 2002, Sole, K. C., Preston, J. S., Cole,
P. M. and Robinson, D. R. (eds.), South African Institute
of Mining and Metallurgy, Johannesburg, pp. 1033-1038.
FOR FURTHER INFORMATION on the work reported or
on the piloting capabilities available at AARL, please contact
Kathy Sole at [email protected] o.za or visit our Web site at
www.aarl.co.za.
Experiment
Model
00
4
8
12
16
20
20 40
[
C u ] o r g
( g / l )
[Cu]aq (g/ l)
60 80
SIMULATIONMODELING
Potential extractant systems that
could achieve the high copper transfers
required for the processing of autoclave
discharge solutions were identified
by simulation modeling, using the
software packages supplied by the
extractant manufacturers (MEUM™from Avecia). A comparison of experi-
mental isotherm data for ACORGA®
M-5774 with the model prediction
shows extremely good agreement
(Figure 1), thereby confirming the
validity of using modeling results for
predictive purposes and the prelimi-
nary selection of extractant composi-
tions and operating conditions.Figure 1. Comparison of experimental data with MEUM model predictions.
Extraction of copper from a synthetic solution (70 g/l Cu, pH 1.6) by 32
vol.% ACORGA M-5774.
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A key component to MEP's success is the ability of the
members of our manufacturing facility in Mt. Pleasant, TN toapply Avecia's values to guide their manufacture of the high-
est quality SX reagent available on the market; to work with
customers to meet tight demand schedules, especially in
times of critical need; and to keep a continual focus on SHE
(Safety, Health, and the Environment).
While much of this appears transparent to our
customers, all of these priorities are extremely important
because all these activities around Mt. Pleasant translate
into assurance of supply both in the short term as well
as the long term.
Manufacturing InnovationAvecia's innovative abilities go beyond new product
development. Avecia engineers applied this innovation to
redesign the reagent manufacturing process in 1993. The
improved process not only delivers a high quality reagent, it
also reduces the generation of hazardous waste from the
reagent manufacturing process. The Avecia patented process
reduced organic effluent by up to 85% compared to all other
practiced manufacturing routes. In the Avecia process, it is
also significant to note that the effluent from the process
contains essentially only benign inorganic salts. This
achievement was recognized through the presentation of a
Queen's Award for Environmental Achievement in 1999.
ManufacturingQuality
Mt. Pleasant Acorga Manufacturing Team, Avecia
•Safety, wh ich i s our number 1 objecti ve
•Givi ng signi fi cant val ue to our customers
th rough our products and servi ce
• Being flexible in meeti ng their needs
Avecia is commit ted to: In October 2002 the Mt. Pleasant site received another envi-
ronmental award for demonstrating outstanding achieve-
ment in environmental protection. The award was present-
ed by the Tennessee Association of Business (TAB) in recog-
nition of the site’s hazardous waste management program.
The Mt. Pleasant facility is ISO 9002 certified. But better
than having the procedures in place as directed by these
standards, Avecia has been able to deliver the highest level of
product quality that the ISO certifications hope to enable a
plant to achieve. Avecia is the only Cu SX reagent supplier
to never have a quality rejection of a delivery. The plant has
also never missed a scheduled reagent production delivery
date. This is due to the special efforts Avecia has made to
design the most robust process possible.
Improvements to the manufacture process and proce-
dures continue today with a focus on improving the safety
of the plant; exceeding environmental/regulatory targets;
and maintaining our high product quality while improv-
ing/maintaining plant reliability.
Quality of the People
The plant was commissioned in 1994 with a strong crewof people who brought the original plant on-line at Mt.
Pleasant within a very short time and met many large order
requirements right from the first months of operation.
Many are still working with the process today. This has
brought a lot of continuity to the plant and helped the focus
of the team remain on efforts to continually improve the
process. There is a procedure for every step of the process
ensuring good communication of what is occurring. Every
change is agreed upon and understood by all members of
the team. The supervisors are on call 24 hours per day to
assist if there is ever a problem.
Cont inued on page 8
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8
Organizational News
Brian Townson Tony Moore
Safety Program
At Avecia, safety is the number one priority. Avecia
employees are proud of their safety performance – but are
always looking for ways to improve. The Safety Through At
Risk Reduction (STARR) program is used to constantly
improve the safety of the plant. The STARR committee iscomposed of volunteer representatives from functions across
the manufacturing site. They work with members of the site
to observe and evaluate how job tasks are completed. Their
outside observations are used to improve the safety of proce-
dures across the plant.
The Acorga plant has never had a lost time accident
since it began operation at Mt. Pleasant. The last OSHA
recordable injury was in M ay of 1995. Not only does this
provide the safest possible work environment for our
employees, it helps guarantee that the facility will be in the
best condition to produce a quality reagent.
Manufacturing Quality continued
Brian Townson, Regional Manager for Australia and Europe,
retired at the end of 2002. Brian was a long service employee
with ICI, Zeneca, and Avecia and played a major role in
MEP's growth, particularly in Australia and China. Brian
chose to kick back in the UK after many years of successfulinternational business activities.
Tony Moore has been promoted to Manager-Australasia,
effective 12/1/02. In this expanded role, Tony will assume
commercial and technical responsibility for this region.
With the expanded geographic remit, additional technical
support will be provided to supplement Tony's activities.
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Avecia Chile Limitada held its fifth
annual Solvent Extraction Technical
Seminar in Iquique, Chile on October 3
and 4, 2002. The two-day seminar
was a remarkable success with much
sharing of invaluable knowledge and
experiences among the SX plant
operators as well as those who work to
support the plants. More than ninetyprofessionals attended the seminar and
their active participation helped make
the seminar a resounding success.
Attendees included professionals
from many different mining compa-
nies, including: C.M . Doña Inés de
Collahuasi; Codelco Norte (Radomiro
Tomic and Chuquicamata); Alliance
Copper; Andina, Salvador; C.M.
Mantos Blancos’ Manto Verde and
Mantos Blancos divisions; Lipesed;
Southern Perú; C.M . Cerro Dominador;
Grupo Milpo Minera RayRock S.A.;
BHP Billiton Escondida and Tintaya
divisions; Grupo Mexico’s Mexicana
de Cobre and Mexicana de Cananea
divisions; and Olympic Dam
from Australia.
In addition to representatives from
mining operations, many organizations
were also represented that support
the mining industry, including:
Kvaerner; Outokumpu; 3M; Oxiquim;
Universidad Técnica Federico Santa
María; Universidad Católica del Norte;
and Universidad Arturo Prat.
Participation in the event further
included authorities such as Mr. Olaff
Olmos, Seremi de Minería Región de
Tarapacá; Mr. Patricio Cartagena,
Executive Vice President of the
Comisión Chilena del Cobre; GIEC
President (International Group for
Copper studies) and Jorge Cristi,
Copper Sales Manager for North
America, Trading and Futures
Markets-Codelco Chile.
In addition to the strong technical
program of presentations from the
various operations, social and cultural
activities were also included. Attendees
enjoyed a dinner and performance of
the Artistic Folk Group from the City
Hall Theater. Attendees toured the
Iquique Port during which Mr. Osvaldo
Castro – Avecia Chile Ltda. and Mr.
Manuel Neira – BHP Billiton Tintaya,
made a presentation of flowers at the
Naval memorial.
Fifth Annual TechnicalACORGA Seminar in Chile
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0
Keith Cramer, Techni cal Special ist, M etal Extraction Products, Phoeni x
Troy Bednarski, Techni cal Special ist, M etal Extraction Products, Phoeni x
Aqueous Continuous: Flexibilityto Maintain Production with
Falling PLS Cu Grade
Without question, phase continuity is an important
consideration in the operation of a copper solvent
extraction circuit. Traditionally, conventional circuit
configurations with flows at or close to design are operated
with the E1 stage aqueous continuous and all other stages
organic continuous. Under design conditions, there are
benefits to operating with these continuities. But imposing
strict rules on stage mixer continuities can constrain howa plant reacts to changing solution conditions, possibly
limiting a plants production capacity and increasing its
operating costs. Running additional extract stages aqueous
continuous can have significant metallurgical benefits that
can reduce an SX plant’s overall operating costs.
Plant Operation Options
In a mature market such as North America, copper ore
grades have fallen steadily over the years at many sites. In
most cases the result of this is a reduction in the copper
concentration in the PLS. In order to maintain production,
increased flow through the leach circuit and solvent
extraction plant is required.
There are many ways that the increased PLS flow can
be processed in the plant depending on both plant capacity
and operational philosophy. One way to categorize these
options is to look at how the resulting mixer continuities
will be affected. Some options are presented below for a
series-parallel circuit that either 1) utilize aqueous continu-ous operation in additional extract stages, or 2) maintain tra-
ditional continuities.
Additional options with flexible mixer
continuity requirements.
• Increase PLS flow to series portion of circuit, with E1S
and E2S extract O:A ratios less than 1:1 (aqueous
continuous). (option 1)
• Increase PLS flow to both series and parallel portions of
the circuit equally, both flows above the organic flow
rate. All extracts operate at an O:A ratio less than 1:1
(aqueous continuous). (option 2)
5000
Option 1: Series-parallel, higher flow to series
9000 9000 6000 6000
organic (6000)
E1S E2S
11.0%
Parallel E1S E2S Parallel
E1S E2S Parallel
E1S E2S Parallel
Option 2: Series-parallel, balanced PLS flow
7500 7500 7500 7500
organic (6000)
E1S E2S Parallel
E1S E2S Parallel
Option 3: Extra PLS flow added directly to E2S m ixer
6000 9000 60003000 6000
organic (6000)
PLS
Raffinate
Organic
Option 4: Series-parallel, higher PLS flow to parallel
6000 6000 9000 9000
organic (6000)
Option 5: Extra PLS flow to E1S, then bypassed d irectly to raffinate
9000 60003000 6000 6000
organic (6000)
Option 6: 3 -parallel PLS streams
5000 5000 50005000 5000
organic (6000)
11.3%
11.5%
11.7%
12.5%
14.3%
Metallurgical Comparison of Flow Distribution Optionsv/ o Required for 90% Recovery
* PLS grade 1 .5 gp l Cu; 6,00 0 gp m m aximum organic flow rate;
series-parallel circuit; 15,000 gpm PLS flow
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• Add extra PLS flow directly to the E2S mixer (if E1S-E2S
advance line is at capacity). (option 3)
• Add extra PLS flow to the parallel stage, operating
at an extract O:A ratio less than 1:1 (aqueous
continuous). (option 4)
Options that maintain traditional continuities.
• Increase organic flow and/or organic recycle to maintain
mixer O:A ratios above 1:1. (Maximum PLS flow limited
by organic flow capacity.)
• Increase PLS flow to E1S stage but bypass the “extra”
flow directly to the raffinate pond rather than
advancing it to E2S. (see table, option 5)
• Operate with 3 parallel PLS feed streams. (option 6)
There are options available to maintain traditional
mixer continuities at increased PLS flow rates, but they
have lower limits to the maximum PLS flow and generally
have higher operational costs. The increased operational
costs come from higher reagent concentrations and higher
chemical transfer of Fe (lower Cu loading). The best
metallurgical and economic options typically involverunning additional extract stages aqueous continuous.
The actual “best” configuration and PLS flow limits
will be a little different for each plant based on its specific
PLS grade and physical flow capacities. In many situations,
the best metallurgical performance is obtained when more
PLS flow is processed through the series portion of the
circuit, generally requiring that the E2S stage run aqueous
continuous (rather than using a higher organic recycle
flow). The unbalanced PLS flow distribution is preferential
metallurgically even under “normal” flow conditions.
(see below).
Of course all plants cannot just push flows higher
without any consequences. Due to physical performanceconstraints, some plants need to run under all-parallel
flow conditions with traditional continuities. But this
is the exception rather than the rule. Cu production
does not necessarily need to be sacrificed due to concerns
about the physical capabilities of the reagent in the plant.
Can this be done in a com m ercial plant?
ACORGA® reagents used in plants today give the
needed operational flexibility to cope with demanding
conditions. It has been repeatedly shown that when a
plant seems to be “pushing the limit” of flow there is
actually more room to give. All of the circuits discussed
above have been, or are currently in use at large commercial
SX operations.
Yes, really, shift the PLS flow to the series not parallel stage.
0.00 0 . 0
0
2 . 0
0
4 . 0
0
6 . 0
0
8 . 0
0
0.38 0.75
Copper in Aqueous phase
Higher PLS flowto series extraction stages
C o p p e r i n O r g a n i c p h a s e
1.13 1.50
Extraction section
0.00 0 . 0
0
2 . 0
0
4 . 0
0
6 . 0
0
8 . 0
0
0.38 0.75
Copper in Aqueous phase
Higher PLS flowto parallel stages
C o p p e r i n O r g a n i c p h a s e
1.13 1.50
Extraction section
Typically in a series-parallel circuit, the recovery of the
parallel stream does not drop very much if you increase the
flow to this stage. Consequently the tendency is to put any
additional PLS flow into the parallel stage. The Cu recovery
is actually higher if you do the opposite – increase the
PLS flow to the series portion of the circuit. (see diagram
options 1 and 4)
When more PLS flow is directed to the series portion of
the circuit, less is directed to the parallel. The Cu recovery
for the parallel stream increases at the new higher O:A
ratio, but this is not where the biggest benefit comes from.
Because of the higher O:A ratio in the parallel stage, the Cu
concentration of the organic that advances to the E2S stage
is lower. The lower Cu loading entering the E2S stage allows
the series portion of the circuit to also achieve a higher
Cu recovery. The overall performance for the train is better.
The McCabe-Thiele diagrams below illustrate the effect of
changing the extract O:A ratios.
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