22.11.2014 Views

Hydrochemistry and energy storage in aquifers - NHV.nu

Hydrochemistry and energy storage in aquifers - NHV.nu

Hydrochemistry and energy storage in aquifers - NHV.nu

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

The heterogeneous reactions of Si02 generally <strong>in</strong>volve an activated complex; the dissolution<br />

reactions are zero-order whereas precipitation is first-order with regard to dissolved silica<br />

(Rimstidt <strong>and</strong> Barnes, 1980; Bird et al., 1986) (see Equations 4 - 7).<br />

where the * <strong>in</strong>dicates the activated complex.<br />

The slower rate of precipitation as opposed to dissolution has led to the widespread use of<br />

dissolved Si as a geothermometer (Fournier <strong>and</strong> Rowe, 1966; Arnorsson, 1975) of water<br />

temperatures at depth <strong>in</strong> geothermal exploration. This reaction rate differential m<strong>in</strong>imizes<br />

Si02 scal<strong>in</strong>g.<br />

3.4 Temperature dependent modell<strong>in</strong>g<br />

Scal<strong>in</strong>g is to be avoided <strong>in</strong> ATES systems because it results <strong>in</strong> <strong>in</strong>creased ma<strong>in</strong>tenance costs<br />

<strong>and</strong> decreased efficiency. Similarly, unnecessary capital costs for treatment should be<br />

avoided. The avoidance of scal<strong>in</strong>g requires that saturation <strong>in</strong>dices for pert<strong>in</strong>ent m<strong>in</strong>erals be<br />

calculated with a significantly greater reliability than is normally required by geochemists<br />

<strong>and</strong> environmental chemists for <strong>in</strong>terpretative studies. Therefore, a major aspect of the U.S.<br />

contribution to Annex VI of the International Energy Agency collaborative research has<br />

been focused on this problem. Solid solution modell<strong>in</strong>g of carbonates <strong>and</strong> ATESgroundwater<br />

mix<strong>in</strong>g models have already been mentioned. The <strong>in</strong>itial effort was to improve<br />

the temperature competence of our geochemical modell<strong>in</strong>g (Smith, 1988). Calculation of<br />

saturation <strong>in</strong>dices can be no more reliable than the aqueous speciation calculations on which<br />

they are based. However, thermodynamic data are conventionally determ<strong>in</strong>ed at 25°C <strong>and</strong><br />

require adjustment for use at higher temperatures. These adjustments can be estimated with<br />

the Van 't Hoff relationship but this estimation procedure often leads to significant error at

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!