“…The reactivity of forsterite and its silicate alteration products has received increasing attention as a potential source material for the divalent cations required to carbonate CO 2 during carbon storage efforts (e.g. Giammar et al, 2005;Oelkers and Schott, 2005;Bearat et al, 2006;Matter et al, 2007;Oelkers et al, 2008;Dufaud et al, 2009;Prigiobbe et al, 2009;Matter and Kelemen, 2009;King et al, 2010;Daval et al, 2011;Guyot et al, 2011;Broecker, 2012;Kohler et al, 2013;Gislason and Oelkers, 2014;Sissmann et al, 2014). This interest has led to a large number of studies aimed at characterizing forsterite dissolution behavior and rates at various fluid compositions and temperatures (Luce et al, 1972;Sanemasa et al, 1972, Grandstaff, 1978, 1986, Murphy and Helgeson, 1987, 1989Blum andLasaga, 1988, Banfield et al, 1990;Walther, 1991, 1992;Casey and Westrich, 1992, Awad et al, 2000, Chen and Brantley, 2000, Rosso and Rimstidt, 2000, Pokrovsky and Schott, 2000a, 2000b, Oelkers, 2001b, Giammar et al, 2005, Hänchen et al, 2006, Olsen and Rimstidt, 2008Davis et al, 2009;Rimstidt et al, 2012;Olsson et al, 2012;Plümper et al, 201...…”