Jökull


Jökull - 01.01.2010, Side 168

Jökull - 01.01.2010, Side 168
A. Stefánsson bilities were selected. The key aqueous species in the data set included H2O, OH−, H+, Na+, K+, Mg2+, Ca2+, Al(OH)4−, Fe2+, Fe(OH)4−, H4SiO4(aq), Ti(OH)4(aq), H2S(aq), SO42−, HCO3−, Cl−, F− and H2(aq). Their Gibbs energy values were selected from Supcrt92 slop07.dat (Johnson et al., 1992), Gun- narsson and Arnórsson (2000), Benezeth et al. (2001), Ziemniak et al. (1993), Hill (1990), Diakonov et al. (1999) and Marshall and Franck (1981). Values for the apparent Gibbs energy formation of secondary minerals were selected from the data sets given by Holland and Powell (1998), Robie and Hemingway (1995), Neuhoff (2000), Arnórsson and Stefánsson (1999), Fridriksson et al. (2001) and Stefánsson and Gíslason (2001). The saturation of the basaltic glass was estimated according to its dissolution mechanism proposed by Oelkers and Gíslason (2001) and Gíslason and Oelk- ers (2003). The mechanism assumes the solubility of the basaltic glass to be controlled by a leached layer enriched in Al and Si that may be approximated as a mixture of amorphous silica and aluminium hydrox- ide. Reaction path modelling calculations were carried out to simulate the interactions of basaltic glass with water. The initial water composition was either that of pure rainwater from Langjökull, Iceland, or dilute non-thermal groundwater from Thingvellir, Iceland, that had gained some alkalinity. The water compo- sition is given in Table 1. The initial water was allowed to react with basaltic glass in accordance with the dissolution rates reported by Gíslason and Oelkers (2003) and saturated sec- ondary minerals in each step allowed to precipitate. Commonly, 0.1 to 1 mol of basaltic glass (∼10 to ∼100 g) was dissolved in 1 kg of water in >1000 steps. The composition of the basaltic glass used for the cal- culations is given in Table 2 and the secondary miner- als incorporated in the calculations are given in Table 3. The effect of acid supply was conducted by addi- tion of CO2 (weak acid) and H2SO4 (strong acid) to the starting solutions with concentrations of 0.1, 1 and 10 mmol/kg. The thermodynamic properties for phyllosilicates and carbonate solid solutions were calculated using the approach of Tardy and Fritz (1981), assuming ideal solid solution behaviour and, in the case of phyl- Table 1. Chemical composition of the starting water composition used in the model calculations. The con- centrations are in µmol/kg. – Upphafleg efnasetnings vatns sem notast var við í líkanreikningum. Efnastyrk- urinn er gefin í míkrómól/kg. Vellankatla ground water Langjökull precipit. Thingvellir, Iceland a Iceland b pH/◦C 7.54/22 6.05/20 Si 256 3.3 Na 269 61.1 K 11.9 1.01 Ca 71 0.7 Mg 38 6.7 Al 1.09 0.046 Fe 0.16 0 Cl 120 60.2 CO2 354 55.1 SO4 15 0 a Gysi and Stefánsson (2010). b Pogge von Strandmann et al. (2008). Table 2. The chemical composition of Stapafell bas- altic glass (after Oelkers and Gíslason, 2001). – Efnasamsetning basaltglers frá Stapafelli (samkvæmt Oelkers and Gíslason, 2001). wt. % SiO2 48.12 TiO2 1.564 Al2O3 14.62 Fe2O3 1.11 FeO 9.82 MnO 0.191 MgO 9.08 CaO 11.84 Na2O 1.97 K2O 0.29 P2O5 0.195 168 JÖKULL No. 60
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