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Dames & Moore, 1999 - USDA Forest Service

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The acid in the water can be removed by interaction of the solutions with other types of minerals, or by<br />

mixing of acidic solutions with waters containing dissolved alkalinity produced by contact with these<br />

minerals. An example is the buffering of acidity by contact with calcium carbonate minerals.. These<br />

control pH at between 6 and 8:<br />

At the Holden Mine, carbonate minerals generally appear to be rare, but alumino-silicate minerals can<br />

potentially buffer acidity, primarily resulting in the release of aluminum, for example, reaction of the<br />

calcium end-member of plagioclase feldspar (anorthite):<br />

The crystallinity of the silicates limits their reactivity. Framework silicates such as feldspars, have<br />

limited reactivity. Layer silicates (for example, chlorite, biotite and sericite) can be very effective buffers<br />

due to their weak crystalline structure. Bioite is a relatively abundant mineral at the Holden Mine. It<br />

consumes acidity, releasing magnesium, iron, aluminum and silica. Diopside, a relatively abundant<br />

mineral at the Holden Mine, also reacts with acid releasing calcium and magnesium.<br />

The aluminum released when alumino-silicates dissolve in acid can be hydrolyzed to aluminum<br />

hydroxide, releasing acidity:<br />

This buffer controls pH at between pH 4 and 5 and commonly results in the formation of pale precipitates<br />

in mine drainage (for example, the 1500-level main portal, P-1 discharge station). These precipitates are<br />

typically amorphous (non-crystalline) and incorporate other elements.<br />

Ferric hydroxide also buffers acidity, though at a level considered undesirable because the pH of 3 to 3.5<br />

is below the pH at which hydroxides of heavy metals such as copper will precipitate. The fenic<br />

hydroxide buffer reaction is:<br />

63.2 Seasonal Leaching Effects<br />

The above processes describe how acidity and metals are possibly released and neutralized by reaction<br />

with nearby minerals. An important component in these interactions is the rate and flow of water. If water<br />

flow is completely absent, the processes largely proceed in isolation. For example, sulfide minerals will<br />

oxidize producing soluble weathering products but the resulting acidity and metal load will remain stored<br />

on the mineral surface. Neutralizing minerals will also slowly weather but the alkalinity produced will<br />

not be available. This is often the case for mine workings and waste rock associated with hard rock metal<br />

mine sites since preferential flow paths (for example, along fractures in the bedrock within the<br />

underground mine) develop. The weathering products remain stored and do not influence leachate quality<br />

unless contacted by water from a storm event or flooding.<br />

\\DMMSEAl\VOLI\COMMOMWP\~WI~~2\m60.~<br />

6- 12<br />

17693M)5019Uuly 21. <strong>1999</strong>:4:11 PMDRAFT FINAL RI REPORT

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