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1. Introduction - Firenze University Press

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penalty, but without separate capture and long transport distances the energy use should at least be<br />

comparable to the capture step of CCGS, of the order of 2-5 GJ/ton CO2 (mainly heat).<br />

In recent years, research into CO2 mineralisation has taken a giant leap forward as demonstrated by<br />

the rate at which new process routes are suggested, patented and in several promising cases<br />

developed to large-scale application [20]. Many of these processes do not require pure CO2, but can<br />

be run with flue gases directly, such as the process routes suggested by Nottingham <strong>University</strong> [21],<br />

Hunwick [22] and also the ÅA route, to be described below in more detail.<br />

Fig <strong>1.</strong> The location of the Meri-Pori power plant, indicated as , and ultramafic rock in Finland.<br />

Also shown a photo of the nickel mine at Hitura and its location, and ultramafic rock findings in<br />

southern Finland at Vammala and Suomusjärvi (circled).<br />

3. Mineralisation of CO2<br />

3.1 - General<br />

Carbon dioxide mineralisation is the general term describing the sequestration of CO2 by reacting it<br />

with Mg- or Ca-containing compounds, to produce stable carbonates. Magnesium in particular is<br />

abundant in the earth’s crust, as silicates such as serpentinite and olivine. Calcium also has a<br />

potential to store significant amounts of CO2, although calcium silicates are not as abundant as<br />

magnesium silicates. In general, the exothermic reaction between magnesium or calcium silicates<br />

and CO2 can be described by reaction <strong>1.</strong><br />

(Mg,Ca)xSiyOx+2y+zH2z(s) + xCO2(g) x(Mg,Ca)CO3(s) + ySiO2(s) + zH2O(l/g) (1)<br />

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