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ZADRA Elution Circuit Optimisation and Operational Experience at the CIL

Plant of Gold Fields Ghana Limited‖, 4 th UMaT Biennial International Mining
and Mineral Conference

Conference Paper · August 2016

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 ZADRA Elution Circuit Optimisation and Operational
Experience at the CIL Plant of Gold Fields Ghana Limited
M. Beyuo and G. B. Abaka-Wood

Beyuo, M. and Abaka-Wood, G.B. (2016). ―ZADRA Elution Circuit Optimisation and Operational Experience
at the CIL Plant of Gold Fields Ghana Limited‖, 4th UMaT Biennial International Mining and Mineral
Conference, pp. MR 161-167.

Abstract
The ZADRA system is another elution process where gold that is adsorbed on to activated carbon is desorbed from the
carbon by a reversal of the adsorption kinetics. The ZADRA elution circuit at Gold Fields Ghana Limited was designed as a
pressure system with an operational pressure set point of 350 kPa. It consists of circulating 3% sodium hydroxide water
based solution up flow through a stationary bed of loaded activated carbon at a flow rate of 64m3/h at a temperature of 125
°C. The process was designed to take about 16 hours to complete 30 elutions per month. The ZADRA process is
characterised by simplicity of system design and operation, with low desorption rates. Manual control is the standard devoid
of the necessity for automated controls and expected low chemical consumption. However, fluctuations in flow and
temperatures recorded during commissioning and operational stages, reduced stripping efficiencies with its concomitant
effect as an extension of the required stripping cycle time. Consequent on the extension of the required stripping cycle time
and high chemical consumption, the ZADRA elution process hardly completed one batch of elution per day. A review on the
basis of the process design as to whether it is a pressure or atmospheric ZADRA was carried out necessitating in the
reduction of the pressure set point to 120 kPa culminating in a complete turnaround in the system‘s performance. Other
changes followed resulting in a reduction of the stripping cycle time to 13 hours completing two batches of elution per day.

Keywords: Elution, ZADRA elution, activated carbon, eluate, electrowinning, heat exchangers
1 Introduction
The CIL Plant of Gold Fields Ghana Limited (GGL)
Tarkwa Mine, currently exploits the tabular
auriferous conglomerates from seven active open
pits Pepe, Awonaben, Teberebie, Akontansi Central,
Akontansi Ridge, Underlap and Kottraverchy. The
CIL plant capacity was increased from 12.3 Mtpa to
13.5 Mtpa in 2014. Further expansions being
considered have the potential to increase the
capacity to 15.5Mtpa (Mineral resources report,
2014). The leaching circuit of the plant is made up
of 17 tanks in which sodium cyanide is used as the
lixiviant whiles activated carbon is introduced to
adsorb the leached gold. The plant employs both the
Anglo American Research Laboratory (AARL) and
ZADRA methods to strip loaded carbon (1000 -1500
g/t Au). The scope of this paper is aimed at
reviewing the performance of the ZADRA elution
circuit from its commissioning year to the end of
2015.
1.1 Review on Gold Elution
A variety of techniques are found in literature on the
recovery of gold from various solution. (Aylmore
and Muir, 2001; Grosse et al., 2003; Syed, 2012;
Van Deventer and Van der Merwe, 1995; Wan et al.,
1993; Yalcin and Arol, 2002). The adsorption of
gold complexes onto activated carbon (AC) is the
basis of modern techniques for gold recovery and it
is proceded by the desorption of adsorbed gold from
activated carbon with an efficient eluant. By means
1
of high temperature and pressure, treatment of gold
loaded AC with concentrated cyanide or caustic
solution followed by elution with potable water,
aurocyanide complex is desorbed from the gold
loaded activated carbon. Temperature is a key
variable in the elution process and temperatures of
100-120°C are necessary to achieve optimum
elution performance (Anon, 2016). A successful
desorption process requires proper selection of
eluants, which strongly depends on the mechanism
of desorption. Selected eluant should be: cost-
effective, eco-friendly and efficient.
The most common commercial techniques for
elution of gold cyanide from activated carbon are
the ZADRA and AARL procedure. In the ZADRA
elution process, hot solutions of 1% weight/volume
(w/v) sodium hydroxide (NaOH) and 0.2% w/v
sodium cyanide (NaCN) are recycled through a gold
cyanide-loaded AC bed for up to 72 h at 95–100 oC
and atmospheric pressure to desorb Au(CN)2. More
recently a modified Zadra procedure operating at
140 oC in a pressurized system has reduced elution
time to 10–12 h (Robles, 2001).
Soleimani & Kaghazchi (2008) sought to investigate
for a rapid, safe, ambient temperature method for
gold stripping from loaded activated carbon. Gold
loaded AC was contacted with a strong base
followed by elution with an aqueous solution
containing an organic solvent to investigate an
improved process for recovering gold from activated
carbon other than ZADRA or AARL methods. Gold
desorption from loaded activated carbon was carried
out using acetonitrile, acetone, methanol,
isopropanol and ethanol. Gold recovery for these
solvents was in the order: acetone > acetonitrile >
methanol > ethanol > isopropanol. It was concluded
that organic solvents could be used to strip gold
from activated carbon which compared well with
both ZADRA and AARL methods (Soleimani and
Kaghazchi, 2008).
van Deventer and van der Merwe (1994) studied the
functional relationship between the effect of pH,
temperature, concentrations of cyanide and cations
on the gold cyanide equilibrium during elution from
activated carbon in columns and in batch reactors.
They identified that the resistance to the mass
transfer were less intense under robust elution
conditions. It was identified that the elution of
aurocyanide was inhibited by the action of cations
through the formation of Mn+(Au(CN)2−) on
activated carbon. Gold desorption conditions namely
high temperatures and intense cyanide pre-
treatment, decreased the sensitivity of gold elution
to flow rate and the radial distribution of the gold
through the carbon particles. (van Deventer and van
der Merwe, 1994).
Boshoff (1994) suggested that the elution efficiency
is independent of the amount of gold present on the
activated carbon. It was proved that cyanide-free
elutions of carbons containing < 1 200 g/t copper,
are indeed possible and that under these conditions
acid wash conditions typically acid concentration
could be reduced without a detrimental effect on
gold elution efficiency (Boshoff, 1994).
ZADRA and AARL processes are known to be
effective in stripping of gold from activated carbon,
but both processes suffer from high-energy
consumption, high capital costs for pressurized
operations, long elution times and the use of
concentrations of environmentally obnoxious
sodium cyanide (Liebenberg and Deventer, 1997;
Soleimani and Kaghazchi, 2008; van Deventer and
van der Merwe, 1994).
2 Overview of CIL Plant (GGL)
ZADRA design parameters
The ZADRA elution circuit at the CIL Plant
constitute various stages including carbon recovery,
acid washing, carbon transfer, column fill, eluant
recirculation, elution and electrowinning, carbon
cooling and discharge with no cyanide addition. The
eluant is continuously circulated through the elution
column and the electrowinning cell in series.
The process begins with recovery of loaded carbon
into the acid wash vessel, where inorganic foulants
are removed using hydrochloric acid. The process
consists of circulating about 3% NaOH solution up
flow through a stationary bed of loaded activated
2
carbon at a flow rate of about 64m3/h at about
125°C. Pregnant eluate from the elution column is
cooled to below boiling point and passed through
the electro winning cells where gold is deposited on
the cathodes. On leaving the electrowinning cell, the
now gold depleted eluate is re-heated before it is
circulated back into the elution column. Achieving
the design electro winning single pass extraction in a
ZADRA elution circuit is critical. Unlike the AARL
elution system, poor single pass extraction in a
ZADRA process has a direct impact on the overall
elution efficiency. The process was designed to last
for about 14 to 16 hours. An elution column
temperature of 125 °C is maintained until the
process is over. Elution and electrowinning as
indicated occurs simultaneously, and solution
circulation and transfer from one stage to the other is
made possible by automated valves. Electrowinning
cells are operated within 750-800 A and 3.8-4.0 V.
The first ZADRA elution process started at the CIL
plant on 21st January 2009 and has since been
running to date.
3 ZADRA Elution Circuit Performance
Review
The scope of the performance review of the ZADRA
elution circuit, covers from the commissioning year
(2009) to the end of 2015. Selected operational
parameters and experiences in the running of the
circuit are presented in this section. Two sections of
performance review are presented; elution start-up
(February, 2009 to December 2012) and
interventions (January, 2013 to December, 2015).
The start-up period mainly discusses the
performance of the circuit from its commissioning to
the end of 2012. The intervention section, on the
other discusses the circuit performance whiles
various changes in operational parameters as a result
of challenges encountered during the start-up period.
For the periods under review, ZADRA elution
circuit performance data have been analyzed and
presented. Operational parameters considered
include gold loaded activated carbon concentration,
eluate flow, caustic concentration, elution duration,
and stripping and electrowinning efficiencies.
3.1 Elution Start-up Performance
In the commissioning year, 2009, a total of 270
elutions were performed, over 11 months,
representing approximately 24.5 elutions/month as
against the design of 30 elutions/month. The number
of elutions increased steadily from the month of
commissioning to the end of the year. The least
number of elutions, 19 was performed in February
and the highest, 32 was in December. On the other
hand, the strip cycle duration was observed to
decrease towards the end of the year. In December,
where the highest number of elutions was
performed, an average of about 16 hours of strip Table 1 Month Average AC Grade, Stripping
cycle was recorded. The longer the strip cycle the and Electrowinning Efficiency Data
less the number of elutions performed. The NaOH (2009).
concentration for the year was generally good,
recording an average of 3.01% with the least MONTH LC grade EC grade SE EE
monthly average concentration of 2.78% obtained in Feb-09 1331.32 164.45 76.96 64.54
February (see Table 2). A general improvement in Mar-09 1363.78 94.36 86.81 72.53
the stripping and electrowinning efficiency as the
Apr-09 1366.82 98.70 86.44 72.87
year progressed was achieved. It is a common
practice to experience fairly low stripping and May-09 1199.39 71.17 91.54 76.77
electrowinning efficiency during start-up of circuits, Jun-09 1181.10 46.83 90.03 78.44
as it takes some time to obtain optimum operating
Jul-09 1392.51 79.13 95.70 83.53
levels. Much stable efficiencies were observed
towards the end of the year. Gold loaded AC Aug-09 1502.75 70.04 89.56 83.25
stripped over the period (2009) averaged about 1372 Sep-09 1482.44 74.62 89.64 83.08
ppm. Month average gold loaded AC grade of 1168 Oct-09 1480.19 98.94 92.55 88.07
ppm was obtained in December, hence the increased
number of elutions (32), and the shorter strip cycle Nov-09 1420.71 78.60 95.03 91.05
period (16.63 hrs.) to compensate
2D Graph 1 for the relatively Dec-09 1168.36 79.80 93.26 84.97
poor gold loading on the AC. Average 1353.58 86.97 89.78 79.92

34 *LC – gold on loaded AC, EC – gold on eluted AC,

SE – stripping efficiency and EE – Electrowinning
32
efficiency.
Elution duration
Elution duration/Number of elution

30
Number of Elutions
28 After commissioning, the ZADRA circuit faced
26 some challenges, which included excessive metal
build-up in eluate, rampant scaling in heat
24
exchangers, blockage of bottom strainers in elution
22 column, excessive pressure build-up, high
20 electrowinning cell feed temperature and poor
18
deposited gold texture and high burn-off.
16
Table 2 Month Average Elution Circuit
14 Parameters (2009).
12 Month NaOH Flowrate, Duration, N
Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec conc., ppm m3/h h
Month, (in 2009)
Feb-09 2.78 28.82 18.21 19
Mar-09 3.07 35.66 16.78 23
Apr-09 3.08 37.37 18.36 22
Figure 1 Elution Duration and Number of May-09 2.89 38.35 20.80 26
Elutions Data in 2009 Jun-09 2.87 36.22 21.00 24
The circuit‘s performance has been summarized in Jul-09 3.21 33.05 22.43 23
Table 1. It is shown that both stripping and Aug-09 3.14 33.72 24.18 25
electrowinning efficiencies generally improved Sep-09 3.27 33.37 17.64 22
across the year (2009). The stripping efficiency
Oct-09 3.11 40.65 20.20 27
showed a much linear trend than electrowinning
efficiency, having an R2 value of 0.8631, as against Nov-09 3.28 37.12 19.33 27
0.5554 for electrowinning efficiency. The data Dec-09 2.83 25.62 16.63 32
indicates that stripping efficiency increased steadily Average 3.05 34.54 19.60 25
between February to July, plateaued between July *N – Number of elutions
and September, and increased in November, and
thereafter decreased marginally. The excessive metal build-up in the eluate may be
responsible for the poor electrowinning efficiencies
encountered over the period under review. These
metals, predominantly copper (Cu) and nickel (Ni)
are competitively deposited on the cathodes of the
electrowinning cells, affecting the electrowinning
efficiency. The year average of electrowinning
efficiency increased from 79.41% to 89.02%

3
between 2009 and 2010, and reduced by
approximately 9 % in 2011 (Fig. 3). The effect of
metal deposition on the cathode of the
electrowinning cell was pronounced in 2011.
Electrowinning samples were analysed and the
results showed significant amount of Cu and Ni
were present in the samples (Table 3). The high
concentration of these metal species were attributed
to co-leaching due to high NaCN concentration used
in the CIL circuit.
Table 3 Metal Distribution in Electrowinning
Samples at 250 ppm NaCN Set-point
(2011).
Metal concentration
Sample
Cu, ppm Ni, ppm
PE Start 22.00 3.20
PE Mid 6.88 2.65
PE End 2.9 1.8
LE 3.22 0.5
BE 4.78 0.5
EW Feed 1.00 1.45
EW Tail 0.2 0.5
*PE – Pregnant Eluate, LE – Lean eluate, BE –
Barren eluate and EW – Electrowinning
Excessive scaling in heat exchangers was one major
challenge the circuit encountered. The scale build up
in the heat exchangers impacted on the elution
temperature control system hence the extended
elution duration. The temperature control system is
automated, hence eluant had to be recirculated for a
longer period to attain the desired temperature. This
also explains why longer elution durations were
observed for less number of elutions relative to the
design. A year average of 19.89 h was taken to
complete approximately 25 elutions/month in 2009.
Excessive production of fine gold loaded AC at the
bottom of the elution column was also a huge
challenge the circuit faced. The high attrition rate of
the loaded AC led to the problem of ‗blinding‘
especially the bottom strainers of the ZADRA
elution column. These near mesh (fine) carbon end
up restricting the flow of eluant through the circuit.
Very poor eluant flow rates were observed from
2009 to 2010. The month average flow rates were
generally < 40 m3/h in 2009 (35.54 m3/h), relative to
64 m3/h per design, whilst in 2010 the average flow
rate was 37.54 m3/h.
Frequent boiling eluate was a norm in the
electrowinning cells in the gold room giving rise to a
very light and fluffy deposited gold texture and high
burn-off after smelting. It is also shown that the
average concentration of NaOH used in 2011 was
generally lower than in the previous year (Figure 2).
Half of the months in the year recorded
concentrations < 3.0%, with the least average of
4
2.03% reported in June. The low concentrations
were mainly as a results of reduction in purity of
NaOH supplied. Low caustic (NaOH)
concentrations may also haveCustic
negative impact on the
stripping efficiency.
4.5
2009
2010
4.0 2011
Design
Caustic concentration, %
3.5
3.0
2.5
2.0
1.5
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
Month
Figure 2 Caustic Concentration Data from 2009
to 2011.
3.2 Interventions
It was realized that the circuit performance was
dependent on the optimization of operating
parameters. Certain parameters had to be
compensated for others, whiles efforts were made to
maintain some parameters within plant design
levels, especially temperature. Along with parameter
changes, improved cleaning and maintenance
regimes were instituted to control/minimize some of
the identified problems.
In order to address the challenges posed by the fine
carbon due to attrition, regular strainer clean-up was
instituted followed, by changing the mesh size of
bottom strainers from 600 µm to 700 µm and as well
as changing the carbon recovery screen mesh size to
1000 µm from 700 µm. Investigations into
identifying and selecting AC brand with lower
attrition rate and high adsorptive capacity were
conducted on seven different AC brands by Abaka-
Wood et al. (2014). This was aimed at revising the
AC brand being used. PICA AC was thus introduced
as it showed optimum attrition rate and adsorption
capacity compared to the other brands investigated
(Abaka-Wood et al., 2014). PICA AC has been
blended with CHEMQUEST AC since the latter part
of 2012 to date. These implementations significantly
aided in reducing the rate of ‗blinding‘ of the bottom
strainers hence improved eluant flow rate. A gradual
increase in flow rate can be seen from Fig. 3. The
year average solution flow rate increased
significantly from 2012 to 2014 and decreased generally above 60 (up to 64) m3/h in accordance
marginally in 2015. The year average flow rates with design. The year average flow rate in 2014 was
recorded were 39.54, 53.52, 61.18 and 54.92 m3/h approximately 61 m3/h. The least month average in
for 2012, 2013, 2014 and 2015, respectively. The 2014 was approximately 58 m3/h in August. It is
increase in the flow rates also resulted in increase in important to note that the shorter elution duration,
the number of elution cycles conducted, as the resulted in generally lower gold loading on activated
increased flow rate reduced the elution duration. carbon, as the residence time of carbon in the CIL
With the exception of 2013, between 2012 and circuit was shortened to keep elution cycle running.
2015, the number of elutions conducted were more The trends in Fig. 4 indicate that the gold loadings
than 30 per month. An average of 40 elutions/month on activated carbon decreased significantly after the
were conducted in 2014, whiles 43 elutions/month period when the changes were implemented (that is
was achieved in 2015. The least year average within 2012). The average year gold loading on the AC for
this period was 28 elution/month in 2013 (due stripping was 1558.68 g/t in 2012, which reduced to
industrial action for 2D2 Graphmonths),
1 whilst 30 1327.67 g/t in 2013, 1159.32 g/t in 2014 and
elution/month was conducted in 2012. 1145.64 g/t in 2015. Stripping efficiency was
70 22 affected especially in 2015, where it reduced by
Number of elutions per month / Elution flow rate

about 2.5 %, relative to 90.1% in 2014. Furthermore,

an effective eluate cooling system and a strict eluate
20
60 temperature controls were put in place. Temperature
at which eluate reports to electrowinning cells which
Elution flow rate
18 Elution duration, h was initially set at 100 °C, was changed to 110 °C to
50 Elutions/month rid the eluate of all volatiles especially oxygen
Elution duration
16
which is particularly obnoxious to gold deposition at
the cathodes. This action not only improved gold
40 deposition but also contributed to the reduction in
14 the overall eluate circulation time. Electrowinning
efficiency was fairly constant between 2012 and
30
12 2014 (about 81%), after2Dwhich
Graph it2 increased to about
86% in 2015.
94 1600
20 10 Stripping Efficiency
2009 2010 2011 2012 2013 2014 2015 Electrowinning Efficiency
Stripping/Electrowinning Efficiencies, %

92 LC Grade
Year

Gold Loaded Carbon Grade, ppm

1500
Figure 3 Elution Flow Rate, Number of 90
Elutions/month and Elution Duration Data
from 2009 to 2015. Vertical line shows year of 88
1400
implementation of interventions.
86

Furthermore, a bi-weekly eluate ‗bleed-off‘ and 1300

84
monthly complete eluate change-out regimes were
instituted which improved stripping efficiency and 82
consequently reduced gold grade on eluted carbon 1200
drastically. This also improved the rate of 80
temperature rise to its set point in the elution
column. A bi-weekly sulphamic acid treatment of 78 1100
heat exchangers was also instituted which also 2008 2009 2010 2011 2012 2013 2014 2015 2016

reduced the regular heat exchanger bundle change- Year

out time of 3 to 8 months at the oil side and 4 to 12
months at the solution side of the heat exchanger. It
was observed that the elution column pressure and Figure 4 Electrowinning Efficiency, Stripping
the flow had an inverse relationship. This is Efficiency and Gold Loaded Carbon Grade Data
maintained by a process control valve. With a high from 2009 to 2015. Vertical line shows year of
set point (intending to be a pressure ZADRA) of 350 implementation of interventions.
kPa, the flow could not exceed 40 m3/hr. The
excessive pressure also forced so many near-mesh In effort to reduce the levels of metal impurities
size carbon particles into the elution column bottom that affect electrowinning efficiency and gold
strainers thereby restricting the flow of eluate deposition, the NaCN concentration set-point
through the column from the heat exchangers. The for leaching at the CIL circuit was reduced to
pressure set point was thus reduced to 120 kPa. This 200 ppm, with gold recovery unaffected.
also contributed massively to optimizing the elution However, the concentration of Cu and Ni in
flow rate. In 2014, the month average flow rate was

5
electrowinning samples analysed were lower assurance on reagents used must also be ensured.
compared to that presented in Table 3. Adherence to the cleaning regimes as instituted
should be ensured to minimize the production of
scales, especially in heat exchangers.

Table 4 Metal distribution in electrowinning

samples at 200 ppm NaCN set-point References
Metal concentration Abaka-Wood, G.B., Asamoah, R.K. and Abbey,
Sample
Cu, ppm Ni, ppm C.E., (2014), "Comparison of Selected
PE Start 9.5 1.06 Activated Carbon Brands‘ Characteristic
Properties for Gold Adsorption – A Case Study
PE Mid 4.81 0.89 at Goldfields Ghana Limited (GGL), Tarkwa
PE End 2.35 0.58 Mine", 3rd UMaT Biennial International
LE 0.26 0.07 Mining and Mineral Conference, Tarkwa,
BE 0.09 0.05 Ghana pp. 187-191.
EW Feed 0.69 0.11 Anon, (2016), "Elution and Carbon Reactivation",
Metalliferous Mining - Processing, 19 pp.
EW Tail 0.14 0.09
Aylmore, M.G. and Muir, D.M. (2001), "Thiosulfate
leaching of gold—a review", Minerals
Engineering, 14(2): 135-174.
4 Key findings and Conclusions Boshoff, P.T.E., (1994), "Cyanide-free AARL
elutions are feasible", Minerals Engineering,
The ZADRA elution circuit was characterized by 7(2): 251-264.
fluctuations in eluate flow, production of fine AC Grosse, A.C., Dicinoski, G.W., Shaw, M.J. and
from gold loaded AC, low desorption rate and Haddad, P.R., (2003), "Leaching and recovery
excess column pressure. Stripping and of gold using ammoniacal thiosulfate leach
electrowinning efficiencies were generally poor, liquors (a review)", Hydrometallurgy, 69(1): 1-
hence their concomitant effect of prolonged 21.
stripping cycle. The system produced poor textured Liebenberg, S. and Deventer, J.V., (1997),
deposited gold and high-burn off, due to the "Evaluating a dynamic model for the
presence of other metals and volatile matter. competitive elution of gold and base metals
from activated carbon", Separation science and
Optimization of NaCN concentration used in the technology, 32(11): 1787-1804.
CIL circuit was necessary in reducing the levels of Robles, A.T., (2001), "Process for eluting precious
Cu and Ni that pose threat to gold deposition on the metals from activated carbon", Google Patents.
cathodes of the electrowinning cells. Regular Soleimani, M. and Kaghazchi, T. (2008), "Gold
strainer clean-up, changing of the mesh size of recovery from loaded activated carbon using
bottom strainers from 600 µm to 700 µm and also different solvents", Journal of the Chinese
changing the recovery screen size to 1000 µm from Institute of Chemical Engineers, 39(1): 9-11.
700 µm, was necessary to control and/eliminate the Syed, S., (2012), "Recovery of gold from secondary
problems posed by fine carbon. Scaling in heat sources—a review", Hydrometallurgy, 115: 30-
exchangers was controlled with the introduction of 51.
the bi-weekly sulphamic acid treatment (de-scaling). Van Deventer, J. and Van der Merwe, P. (1995),
The elution column pressure and flow rate have "Kinetic model for the decomposition of
inverse relationship. With a high pressure set point, cyanide during the elution of gold from
the elution flow rate could not exceed 40 m3/h, activated carbon", Separation science and
hence reduction in the pressure set point saw the technology, 30(6): 883-898.
flow increasing up to 64 m3/h in accordance with van Deventer, J.S.J. and van der Merwe, P.F.,
design. The temperature of eluate reporting to the (1994), "Factors affecting the elution of gold
electrowinning cell was set to 110 °C to eliminate cyanide from activated carbon", Minerals
significant amount of volatiles especially oxygen. Engineering, 7(1): 71-86.
Wan, R.Y., Le Vier, M. and Miller, J.D. (1993),
"Research and development activities for the
5 Recommendations recovery of gold from non-cyanide solutions",
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An effective eluate cooling system and a strict eluate 415-436.
temperature controls must be adhered to, to ensure Yalcin, M. and Arol, A.I. (2002), "Gold cyanide
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6
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Authors

Martin Beyuo, CIL and Extraction Superintendent at Gold

Fields Ghana Limited, Tarkwa. He obtained both MPhil (2013)
and BSc (2005) degrees in Minerals Engineering from the
University of Mines and Technology (UMaT), Tarkwa. He has
worked as an Assay Technician at Precious Minerals Marketing
Company Limited (PMMC), Ghana (1996-2005). His research
interests are in CIL operations and gold desorption from activated
carbon.

George Blankson Abaka-Wood, PhD

candidate at the Future Industries Institute of
the University of South Australia, Australia.
He holds a BSc degree in Minerals
Engineering from the University of Mines
and Technology, Tarkwa (2011). He was a
research assistant at Process Innovation,
Ghana (2011). George, worked as a Metallurgist at the CIL Plant
of Gold Fields Ghana Limited, Tarkwa Mine (2012 – 2014). His
research interests are in Rare earth elements minerals
beneficiation, Comminution and CIL plant optimization issues.

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