Far from equilibrium enstatite dissolution rates in alkaline solutions at earth surface conditions

2011 ◽  
Vol 75 (23) ◽  
pp. 7486-7493 ◽  
Author(s):  
Sougata Halder ◽  
John V. Walther
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Tsing Bohu ◽  
Ravi Anand ◽  
Ryan Noble ◽  
Mel Lintern ◽  
Anna H. Kaksonen ◽  
...  

Science ◽  
1971 ◽  
Vol 173 (3996) ◽  
pp. 533-535 ◽  
Author(s):  
F. T. Mackenzie ◽  
R. Gees

2014 ◽  
Vol 78 (6) ◽  
pp. 1449-1464 ◽  
Author(s):  
Tamara Diedrich ◽  
Jacques Schott ◽  
Eric H. Oelkers

Steady-state tremolite dissolution rates, at far-from-equilibrium conditions, were measured as a function of aqueous silica and magnesium activity, pH from 1.9 to 6.7, and temperature from 25 to 150ºC. Calcium is released from tremolite faster than either Mg or Si throughout most of the experiments even after these latter elements attained steady-state release rates. The preferential removal of Ca releases fine Mg-Si rich needle-like fibres from the tremolite, probably promoting its toxicity. In contrast, Mg was released in stoichiometric or near to stoichiometric proportion to Si once steady-state was attained. Measured steady-state tremolite dissolution rates based on Si release can be described using where r+ signifies the BET surface area-normalized forward tremolite steady-state dissolution rate, AA refers to a pre-exponential factor = 6610–3 mol cm–2 s–1, EA designates an activation energy equal to 80 kJ mol–1, R represents the gas constant, T denotes absolute temperature, and ai refers to the activity of the subscripted aqueous species. This rate expression is consistent with tremolite dissolution rates at acidic pH being controlled by the detachment of partially liberated silica tetrahedra formed from the exchange of Mg2+ for two protons near the mineral surface after the near-surface Ca has been removed. Nevertheless, Mg release rates from tremolite are ~3 orders of magnitude slower than those from forsterite and enstatite suggesting that tremolite carbonation will be far less efficient than the carbonation of these other Mg-silicate minerals.


2015 ◽  
Vol 168 ◽  
pp. 222-235 ◽  
Author(s):  
Eric H. Oelkers ◽  
Liane G. Benning ◽  
Stefanie Lutz ◽  
Vasileios Mavromatis ◽  
Christopher R. Pearce ◽  
...  

2008 ◽  
Vol 72 (1) ◽  
pp. 155-158 ◽  
Author(s):  
S. Gudbrandsson ◽  
D. Wolff-Boenisch ◽  
S. R. Gíslason ◽  
E. H. Oelkers

AbstractFar-from-equilibrium dissolution rates of crystalline basalt were measured in a mixed-flow reactor at pH 4 and 10, and at temperatures from 25 to 75ºC. The material used was obtained from a dyke on Stapafell Mountain on Reykjanes peninsula in Iceland because of its similarity with previous experiments on dissolution rates on basaltic glass by Oelkers and Gislason (2001) and Gislason and Oelkers (2003). Comparison of dissolution rates of basaltic glass and of crystalline basalt of similar chemical composition (from Gislason and Oelkers, 2003) indicates lower rates for crystalline material.


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