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geothermal resource potential of the safford-san simon basin, arizona

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Equation (1)<br />

Alumino-silicate + H 2<br />

C0 3<br />

(solid)<br />

Cations + HC0 3<br />

+ Si (OH)4 + kaolinite<br />

(solid)<br />

where H 2<br />

C0 3<br />

= CO (g) 2<br />

+ H29<br />

Si (HO)4 is dissolved silica<br />

Comparisons <strong>of</strong> calculated dissolved carbon dioxide concentrations with silica<br />

concentrations in all three types <strong>of</strong> ground water in <strong>the</strong> Cactus Flat-Artesia<br />

area suggest that a steady-state disequilibrium with alumino-silicates and<br />

quartz has a more important influence on silica concentration than does temperature-dependent<br />

equilibrium with quartz (Figure 24).<br />

Calculation <strong>of</strong> dissolved<br />

carbon dioxide was accomplished using equation (2) from Paces (1972).<br />

Equation (2)<br />

-log pC0 2<br />

= pH-log HC0 - 3<br />

7.689 - (4.22 x lO-3T) - (3.54 x lO-5T2)<br />

where T = Temperature<br />

a<br />

C<br />

and concentration :<br />

activity<br />

Silica analyses were corrected for ionization at higher pH because analyses<br />

report total silica.<br />

Silica (Si(OH)4) derived from dissolution <strong>of</strong> quartz<br />

or alumino-silicates dissociates to form SiO (OH);, which at higher pH becomes<br />

an important form <strong>of</strong> dissolved silica.<br />

The following equation is used to<br />

correct for silica ionization:<br />

Equation (3)<br />

log Si (OH)4<br />

corrected<br />

log Si (OH)4<br />

analyzed<br />

log Si (OR);<br />

dissociated<br />

where log Si (OH);<br />

equation (4)<br />

and concentration ~<br />

= - 720.15 - 7.3 + pH + log Si (OH)4<br />

273.15 + TOC<br />

analyzed<br />

activity<br />

Equation (4) is derl\Ted in Appendix 2.<br />

65

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