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