Thermodynamic characteristics and mineral dissolution model of the H2O-CO2-CaCO3-Albite-SiO2 system in sedimentary basins

Fuel ◽  
2022 ◽  
Vol 308 ◽  
pp. 121992
Author(s):  
Wei Meng ◽  
Fenggui Sui ◽  
Xuefeng Hao ◽  
Shoupeng Zhang ◽  
Yue Jiang ◽  
...  
Geofluids ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-20 ◽  
Author(s):  
Sergio A. Bea ◽  
Danyang Su ◽  
K. Ulrich Mayer ◽  
Kerry T. B. MacQuarrie

Geochemical conditions in intracratonic sedimentary basins are currently reducing, even at relatively shallow depths. However, during glaciation-deglaciation events, glacial meltwater production may result in enhanced recharge (Bea et al., 2011; and Bea et al., 2016) potentially having high concentrations of dissolved oxygen (O2). In this study, the reactive transport code Par-MIN3P-THCm was used to perform an informed, illustrative set of simulations assessing the depth of penetration of low salinity, O2-rich, subglacial recharge. Simulation results indicate that the large-scale basin hydrostratigraphy, in combination with the presence of dense brines at depth, results in low groundwater velocities during glacial meltwater infiltration, restricting the vertical ingress of dilute recharge waters. Furthermore, several geochemical attenuation mechanisms exist for O2, which is consumed by reactions with reduced mineral phases and solid organic matter (SOM). The modeling showed that effective oxidative mineral dissolution rates and SOM oxidation rates between 5 × 10−15 and 6 × 10−13 mol dm−3 bulk s−1 were sufficient to restrict the depth of O2 ingress to less than 200 m. These effective rates are low and thus conservative, in comparison to rates reported in the literature. Additional simulations with more realistic, yet still conservative, parameters reaffirm the limited ability for O2 to penetrate into sedimentary basin rocks during a glaciation-deglaciation event.


Clay Minerals ◽  
1986 ◽  
Vol 21 (4) ◽  
pp. 711-733 ◽  
Author(s):  
A. C. Morton

AbstractHeavy-mineral studies on Jurassic sandstones from the central and northern North Sea areas and from the Lossiemouth Borehole (onshore NE Scotland) show that the dissolution of apatite is a function of depositional environment rather than burial depth. In the shallow marine Upper Jurassic sands of the Claymore, Clyde and Tartan Fields, and in the deeper-water Magnus sands, apatite is ubiquitous, even where burial depths exceed 3800 m. Conversely, the fluvio-deltaic sands of the Beatrice, Heather, Ninian and Murchison Fields, and of the Lossiemouth Borehole, have suffered apatite dissolution, although burial depths range from very shallow (Lossiemouth Borehole) to about 3300 m. This clearly indicates that apatite dissolution has taken place through penetration of low-pH meteoric groundwaters at a very early stage in diagenesis, and that high-temperature fluids circulating in deep burial have had little or no effect. This is in accord with patterns of mineral dissolution observed in other sedimentary basins and in the North Sea Palaeocene. Although dissolution of heavy minerals is unlikely to generate significant secondary porosity, the process is nevertheless caused by the same pore-fluids that dissolve major framework constituents. Patterns of heavy-mineral dissolution therefore provide clues to the nature of these pore-fluids. Here, the relative stability of apatite is particularly significant. The order of stability apatite > garnet > kyanite, which characterizes deep burial of North Sea sandstones, has previously been simulated experimentally using fluids of pH 8 at room temperature. This suggests that high-temperature acidic pore-fluids may not have played a significant role in the development of secondary porosity in North Sea sandstones.


2000 ◽  
Vol 12 (3-4) ◽  
pp. 219-226 ◽  
Author(s):  
P. Bellingham ◽  
N. White

Author(s):  
I. Khidirov ◽  
V. V. Getmanskiy ◽  
A. S. Parpiev ◽  
Sh. A. Makhmudov

This work relates to the field of thermophysical parameters of refractory interstitial alloys. The isochoric heat capacity of cubic titanium carbide TiCx has been calculated within the Debye approximation in the carbon concentration  range x = 0.70–0.97 at room temperature (300 K) and at liquid nitrogen temperature (80 K) through the Debye temperature established on the basis of neutron diffraction analysis data. It has been found out that at room temperature with decrease of carbon concentration the heat capacity significantly increases from 29.40 J/mol·K to 34.20 J/mol·K, and at T = 80 K – from 3.08 J/mol·K to 8.20 J/mol·K. The work analyzes the literature data and gives the results of the evaluation of the high-temperature dependence of the heat capacity СV of the cubic titanium carbide TiC0.97 based on the data of neutron structural analysis. It has been proposed to amend in the Neumann–Kopp formula to describe the high-temperature dependence of the titanium carbide heat capacity. After the amendment, the Neumann–Kopp formula describes the results of well-known experiments on the high-temperature dependence of the heat capacity of the titanium carbide TiCx. The proposed formula takes into account the degree of thermal excitation (a quantized number) that increases in steps with increasing temperature.The results allow us to predict the thermodynamic characteristics of titanium carbide in the temperature range of 300–3000 K and can be useful for materials scientists.


Sign in / Sign up

Export Citation Format

Share Document