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A trial of extracting gold from stream sediment and High Au/Ag ore ...

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A <strong>trial</strong> <strong>of</strong> <strong>extracting</strong> <strong>gold</strong> <strong>from</strong> <strong>stream</strong><br />

<strong>sediment</strong> <strong>and</strong> <strong>High</strong> <strong>Au</strong>/<strong>Ag</strong> <strong>ore</strong><br />

using halogen-containing<br />

organic system<br />

H. Murakami <strong>and</strong> Y. Nakao<br />

Institute for Geo-Resources <strong>and</strong> Environment, AIST<br />

Geological Survey <strong>of</strong> Japan


Contents<br />

Why did we chose this theme?<br />

( Meaning <strong>and</strong> Purpose )<br />

Outline <strong>of</strong> method using halogen-containing organic<br />

system<br />

Rough experiment <strong>of</strong> dissolution/deposition <strong>of</strong> <strong>gold</strong><br />

Application for <strong>stream</strong> <strong>sediment</strong> <strong>and</strong> <strong>ore</strong><br />

Summary


Man-made<br />

pollution<br />

• <strong>gold</strong>-mercury amalgamation<br />

Even in m<strong>ore</strong> recent times, mercury<br />

has been employed to extract <strong>gold</strong> in<br />

the small-scale mining. (e.g.<br />

Philippine, Brazil). Procedure <strong>from</strong><br />

creating amalgams with mercury<br />

through heating to drive <strong>of</strong>f mercury,<br />

results in a large number <strong>of</strong><br />

POISONINGs that attack to local<br />

people.<br />

View <strong>of</strong> high-grade Hg <strong>sediment</strong>s at the river (Murao, 2003).


<strong>Ag</strong>ainst cyanide leaching<br />

Tailing <strong>of</strong> waste <strong>from</strong> Cyanide-leaching<br />

• In case <strong>of</strong> <strong>extracting</strong> <strong>gold</strong> by using<br />

cyanide, cyanide-solution is quite<br />

dangerous for worker to treat.<br />

• Waste <strong>of</strong> cyanide-leaching process,<br />

especially aerosol <strong>from</strong> leaching<br />

pads has potential to damage the<br />

environments.<br />

• It takes too much time to extract<br />

<strong>gold</strong><br />

(several tens hour in usual)


Purpose<br />

• If we can establish another harmless technique to extract<br />

<strong>gold</strong>, that will be m<strong>ore</strong> effective for the above situations.<br />

• Halogen-containing organic solvent systems (HOS), wellknown<br />

as “tincture <strong>of</strong> iodine” can serve as good solvents<br />

for noble metal such as <strong>gold</strong>. Tincture <strong>of</strong> iodine is easy to<br />

h<strong>and</strong>le <strong>and</strong> poisoning-free as can be used for sterilizer.<br />

• Gold can be precipitate by adding ascorbic acid, wellknown<br />

as “Vitamin-C” into such a solvent containing<br />

<strong>gold</strong>.<br />

• In order to find some criteria in these phenomenon, we<br />

have here examined dissolution/deposition experiments<br />

with HOS <strong>and</strong> ascorbic acid.<br />

Tincture <strong>of</strong> iodine<br />

(HOS)


Outline <strong>of</strong> method<br />

using halogen-containing organic system<br />

(HOS)<br />

•Dissolution<br />

In our experiments, HOS is composed <strong>of</strong> I 2 , NaI <strong>and</strong> ethanol. A<br />

triiodide ion, I 3 - is isolated <strong>from</strong> this system <strong>and</strong> active for the<br />

dissolution <strong>of</strong> metal. A dark brown color <strong>of</strong> the system reflects<br />

presence <strong>of</strong> I 3 - .<br />

I 2 +I - (in NaI) ⇔ I 3<br />

-<br />

The I 3- ion is effective oxidant toward noble metal, <strong>and</strong> in the<br />

presence <strong>of</strong> I - , reacts with <strong>gold</strong> to form the very stable [<strong>Au</strong>I 4 ] -<br />

complex.<br />

2<strong>Au</strong> + 3I 3- ⇔ 2[<strong>Au</strong>I 4 ] - +I -


•Deposition<br />

After <strong>gold</strong> is dissolved, ascorbic acid is added to reduce I 2 .<br />

I 2 ⇒ 2I -<br />

This reduction results in deficiency <strong>of</strong> I 3 - , HOS begins to<br />

behave as “poor-solvent” for <strong>gold</strong>. A dark brown color <strong>of</strong> HOS<br />

is lost reflecting depletion <strong>of</strong> I 3 - . Gold can be precipitated.<br />

Hydrogen peroxide liquid (H2O2) can be oxidized the above solution.<br />

2 I − → I 2<br />

The system turns into original HOS which can dissolve <strong>gold</strong>.


Rough experiment <strong>of</strong><br />

dissolution/deposition <strong>of</strong> <strong>gold</strong><br />

In order to estimate dissolution rate <strong>of</strong> <strong>gold</strong> in HOS <strong>and</strong> how much<br />

ascorbic acid needs to be precipitated <strong>gold</strong>, model experiment has been<br />

carried out.<br />

1. A <strong>gold</strong> wire (ca. 1m, 0.2mm in diameter) was added into HOS<br />

(40ml) <strong>of</strong> I 2 (6mmol), NaI (6mmol) <strong>and</strong> ethanol (29.1g) with<br />

stirring at room temperature.<br />

2. After a hour, 10 ml HOS containing <strong>gold</strong> was separated, <strong>and</strong> used<br />

for deposition experiments using ascorbic acid <strong>and</strong> water.


1. Dissolution<br />

This graph shows dissolution <strong>of</strong><br />

<strong>gold</strong> into HOS with time. In first<br />

a hour, there is immediate sharp<br />

rise in dissolution <strong>of</strong> <strong>gold</strong>. After a<br />

hour, dissolution <strong>of</strong> <strong>gold</strong> slightly<br />

increase. It is likely to achieve<br />

equilibrium.<br />

If <strong>gold</strong> was saturated in 0.1g at<br />

room temperature, It can be<br />

estimated 0.1mol <strong>of</strong> <strong>gold</strong> can<br />

dissolve in HOS with I 3-<br />

<strong>of</strong> 1mol.<br />

The increase temperature caused<br />

a rapid growth <strong>of</strong> dissolution <strong>of</strong><br />

<strong>gold</strong>.


2. Deposition<br />

In order to check a condition for<br />

deposition <strong>of</strong> <strong>gold</strong> <strong>from</strong> HOS, water<br />

<strong>and</strong> ascorbic acid were added step by<br />

step. Intervals <strong>of</strong> each step are around<br />

20 minutes.<br />

This graph shows variation <strong>of</strong><br />

concentration for water <strong>and</strong> ascorbic<br />

acid in HOS with 0.175% <strong>of</strong> <strong>gold</strong>.<br />

At 1st <strong>and</strong> 2nd steps, <strong>gold</strong><br />

precipitation did not occur, however<br />

I 3-<br />

ion was lost. Deposition <strong>of</strong> <strong>gold</strong><br />

starts at high water content with<br />

making fine-grained particles.


Bef<strong>ore</strong> application<br />

Rough experiments here indicates that;<br />

1. HOS can be used to extract <strong>gold</strong>.<br />

2. Dissolution rate <strong>of</strong> <strong>gold</strong> reaches to the maximum in the first<br />

one hour.<br />

3. It can be estimated 0.1mol <strong>of</strong> <strong>gold</strong> can dissolve in HOS<br />

with I 3- <strong>of</strong> 1mol. It means that <strong>gold</strong> can be dissolved up<br />

until around 0.1% order <strong>of</strong> <strong>gold</strong> content in the system.<br />

4. By using ascorbic acid, deposition <strong>of</strong> <strong>gold</strong> is likely to be<br />

controlled by water content. Because ascorbic acid can be<br />

dissolve only in system including water.


Application for <strong>stream</strong> <strong>sediment</strong> <strong>and</strong> <strong>ore</strong><br />

In Japan, there are a lot <strong>of</strong> placer <strong>gold</strong><br />

regions. Of these, Kitakami mountain area<br />

in northern part <strong>of</strong> Japan represents<br />

mesothermal <strong>Au</strong> deposits which is<br />

characterized by production <strong>of</strong> native <strong>gold</strong>.<br />

Its <strong>Au</strong>/<strong>Ag</strong> ratio is generally ranges <strong>from</strong> 800<br />

to 950.<br />

Samples <strong>of</strong> <strong>stream</strong> <strong>sediment</strong> <strong>and</strong> <strong>ore</strong> were<br />

taken <strong>from</strong> Kitakami region.


Flow chart <strong>of</strong> experiments<br />

Samples<br />

• Pulverized auriferous quartz vein<br />

• Sieved <strong>stream</strong> <strong>sediment</strong>s (particles<br />

under 0.063mm in diameter)<br />

• HOS is composed <strong>of</strong> I 2<br />

, NaI <strong>and</strong><br />

ethanol.<br />

• Solutions after dissolution <strong>of</strong> sample<br />

<strong>and</strong> addition <strong>of</strong> ascorbic acid were<br />

analyzed by ICP-MS.<br />

• Sample dissolved by 100cc <strong>of</strong> HOS<br />

were carried out for 2 cycles, that by<br />

10cc for 1 cycle.


Sample:solvent=5g:100cc


Sample: solvent=5g:10cc<br />

Deposition<br />

<strong>of</strong> <strong>Au</strong>


Summary<br />

• It is necessary to consider volume ratio <strong>of</strong> sample / solvent in case<br />

<strong>of</strong> <strong>extracting</strong> <strong>gold</strong> <strong>from</strong> natural sample (showing low <strong>gold</strong> grade).<br />

Expected concentration <strong>of</strong> <strong>gold</strong> in HOS should be m<strong>ore</strong> than<br />

1000ppb <strong>of</strong> <strong>gold</strong>.<br />

• Gold in natural materials should be concentrated at the time <strong>of</strong><br />

sampling <strong>and</strong> preparation stage. (e.g. pan concentrate <strong>of</strong> <strong>stream</strong><br />

<strong>sediment</strong>s)<br />

• After the recycling HOS by H 2 O 2 , it seems that Mn <strong>and</strong> Fe<br />

occasionally prevent <strong>gold</strong> <strong>from</strong> <strong>extracting</strong> into HOS.<br />

• Using ascorbic acid to precipitate <strong>gold</strong> is disadvantage to recycling<br />

system due to its requirement water for dissolution into HOS.

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