1.
1 VAT LEACHING PROCESS
Vat leaching is a low cost process method used to treat low-grade gold ores, mine waste material,
or deposits too small to justify construction of milling facilities. The ore is flooded with the
cyanide solution for a lengthy period of time and the leaching solution will dissolve the gold and
silver. The pregnant liquor will be collected as it percolates out from the base of the Vat and sent
to the metal recovery circuit where the precious metals will be removed. (Kappes, 2002)
Gold is extracted by dissolving or leaching it with a solution of sodium cyanide (NaCN) until the
gold in solution falls to 0.20 g/t or below. In Zimbabwe, sodium cyanide is mostly used because
of its availability. In most cases, several leaching stages may have to be carried out before the
gold level in solution falls to the above stated value. In the first leaching stage; to the mass of
sample at hand (usually 10 kg), the mass of water added is 70% that of the sample. That is, if we
have 10 kg sample, 7 kg or 7000g of water is added. Sodium cyanide, lime (CaO) and lead
nitrate (Pb(NO3)2) are then added. The purpose of sodium cyanide is to dissolve the gold and
lime is added to neutralize the acidic constituents of the sample and to adjust the pH to at least
above 9 so that none of the noxious hydrogen cyanide fumes are evolved when sodium cyanide
is added. Lead nitrate is added to provide oxygen, which is essential for this operation. The
reaction is thought to occur as follows:
4Au(s) + 2H20(l) + 8CN-(aq) + O2(g) 4[Au(CN)2]-(aq) + 4OH-(aq)
The amount of lime added corresponds to the acidity or alkalinity of the sample. Samples that are
grayish or whitish are usually less acidic and thus do not require much lime, usually 15-20g per
10 kg of sample. The brownish or reddish samples are associated with iron oxides (particularly
haematite) and hence are considered more acidic. To these, a larger amount (30-40g per 10kg of
sample) of lime is added. Sodium cyanide is added to the sample at a concentration of 0.1%-
potassium cyanide equivalent. This concentration is chosen as it is the one at which the effective
dissolution of gold in cyanide usually occurs.
The amount of sodium cyanide added is calculated as follows (assuming that we are using a10kg
sample and hence 7000g of water):
Mass of NaCN required =0.1/100×7000×0.77
=5.4g
(where 0.77 is a conversion factor from KCN to NaCN)
The mixture is left for about 16 hrs before the solution is drained and weighed. Part of the
solution is sent for assaying (in a vial) and about 10 ml of it is used in titrating for the percentage
of CaO and percentage of KCN. %CaO is determined by titrating the solution with oxalic acid
(H2C2O4) and %KCN with silver nitrate (AgNO 3).If no lime is left in solution more is added.
From the assaying results if, as is usually the case, by the first stage of leaching the gold content
of the solution does not drop to 0.20g/t or below, more leaching stages are carried out. These are
done using 5kg (per 10kg of sample) of water, NaCN of 0.06% KCN concentration equivalent
and appropriate amounts of lime.
The mass of NaCN added in each of these stages is calculated as shown below:
Mass of NaCN required =0.06/100 × 5000 ×0.77
=2.3g
After every 24 hrs, the procedure, as described above, is carried out until the gold level in
solution falls to 0.2g/t or below. At each leaching stage, one tenth of the drained solution is
separated and kept in a bottle. This is mixed with corresponding solutions drained from other
leaching stages. The mixture so formed is called COMPOSITE SOLUTION. At the end of the
leaching operation, this solution is assayed and the result is used in verifying other extraction
results obtained. The assay value of this solution is also used in calculation #7 below:
1.2 CALCULATIONS
1. Head Assay (usually given). This is the amount of gold in the as-received sample in g/t. If not
given or when the sample to be leached is a blend, the head assay is calculated in the ratio of the
blended product as follows;
(AV1× % product 1 + AV2 × % product 2 +……+ AVn * % product n)
where AV1, AV2,…,AVn = the assay values of the blended products 1,2….n respectively.
2. Residue Value (given from the Fire Assay Section). This is the gold that remains in the
sample after leaching, also in g/t.
3. Extraction Value. Calculated as a percentage as follows:
(Head Value – Residue Value) x100%
Head value
4. Extraction by solution (given in g/t) is obtained by adding all the daily extraction values or
by taking the final cumulative extraction value from the table.
5. Composite solution value (given in g/t); is the assay value of the composite solution in the
tab AND
Extraction (Ext) = Composite solution value × L/S ratio (g/t)
6. Ratio: solution/charge or liquid/solid (L/S) ratio
L/S Ratio = Mass of water added excluding wash water (g)
Mass of charge (10 000g)
7. NaCN consumed, calculated in kg/t of the sample of ore leached
SUM of all cyanide added MINUS SUM of (Solution off × % KCN × 0.77/100 at each stage)/10
(including wash water).
OR
If the results do not agree or tie up, a titration of the composite solution is done to determine
the average value of %KCN. This value is then substituted for %KCN in the equation above.
8. Lime required = Total lime added (kg) × 1000
Total mass of sample (kg)
9. Leaching period = number of leaching days + number of washing days (usually one).
10. Calculated AA. (Atomic Absorption) value (g/t) :- It is calculated as follows :
The SUM of (SOLUTION OFF × AV) (at each stage)
(Sum of SOLUTION OFF at each stage) (Excluding wash water)
11. F.A. (Fire Assay) value (g/t):- It is the assay value figure obtained after fire assaying about
150 ml of the COMPOSITE SOLUTION.
the corresponding (F.A.) extraction = F.A. value × L/S ratio (g/t)
NB: The calculated AA. And the FA values are usually used for cross-checking so they are only
used if the extraction by solution and composite solution values do not tie up.
12. Extraction (g/t) = SOLUTION OFF × AV
Mass of sample (10 000g)
13. Cumulative extraction is calculated from the table, (in g/t), as the SUM of (extraction at
each stage).
o VAT LEACHING FOR OPTIMIZATION OF CN CONCENTRATION
In this method, gold is extracted by dissolving or leaching it with a solution of sodium cyanide
(NaCN) until the gold in solution falls to 0.20 g/t or below. In Zimbabwe, sodium cyanide is
mostly used because of its availability. In most cases, several leaching stages may have to be
carried out before the gold level in solution falls to the above stated value. In the first leaching
stage; to the mass of sample at hand (usually 10 kg), the mass of water added is 70% that of the
sample. That is, if we have 10 kg sample, 7 kg or 7000g of water is added. Sodium cyanide, lime
(CaO) and lead nitrate (Pb(NO3)2) are then added. The purpose of sodium cyanide is to dissolve
the gold and lime is added to neutralize the acidic constituents of the sample and to adjust the pH
to at least above 9 so that none of the noxious hydrogen cyanide fumes are evolved when sodium
cyanide is added. Lead nitrate is added to provide oxygen, which is essential for this operation.
Reagents and apparatus
Sodium cyanide
Lime
Lead nitrate
Ore sample and water
20l buckets
AAS machine
Titration apparatus
Procedure
1. Weigh 10 kg of the sample for vat leaching
2. Mix the sample with lime, 15 – 20 grammes for greyish samples and 30-40 grammes
for reddish-brown samples.
3. Charge the weighed sample into a vat leaching tank
4. Weigh 7kg of water and mix with varied amounts of sodium cyanide, 0.5grammes
Lead Nitrate and charge into the vat leaching tank and leave for 16 hrs.
5. Drain the solution and weigh.
6. Take one tenth of the solution and put in a bottle to make up a composite solution.
7. Take a vial of the solution for assaying of gold, 10ml to titrate for lime and free
cyanide
8. Weigh 5kg of water; mix with varied amounts of sodium cyanide, charge into the
leaching tank and drain the solution after 16 hrs.
9. Repeat the procedure as in 6 and 7 until the gold in solution falls below 0.2g/t.
10. Charge 5kg water into the vat leach tank to wash the sample.
11. Drain after 16hrs and titrate for free cyanide.
12. Dry the sample, cone and quarter, and then send a sample for fire assaying.