Effect of water–rock interaction on the morphology of a rock surface

2010 ◽  
Vol 47 (5) ◽  
pp. 816-822 ◽  
Author(s):  
Yu Chen ◽  
Ping Cao ◽  
Rui Chen ◽  
Yun Teng
Processes ◽  
2018 ◽  
Vol 6 (10) ◽  
pp. 199 ◽  
Author(s):  
Xiaojie Yang ◽  
Jiamin Wang ◽  
Dinggui Hou ◽  
Chun Zhu ◽  
Manchao He

Taking Nanfen open-pit iron mine in Liaoning Province as the engineering background, this study analyzes the effect of water-rock circulation on the mechanical properties of rock through a combination of macro-mechanical experiments and microstructure tests in the laboratory. Uniaxial compression experiments and acoustic wave tests are used to determine the degradation law of the mechanical properties of chlorite under the periodic action of water. The experimental results show that dry-wet cycles have a continuous and gradual effect on the rock sampled: Its uniaxial compressive strength, elastic modulus, and acoustic velocity all decrease gradually with an increase in the number of cycles. After 15 wet-dry cycles, the uniaxial compressive strength and elastic modulus of the rock decreased by 34.21% and 44.63%, respectively. Electron microscope scans of the rock indicate that the particle size, characteristics, and pore distribution at the rock surface had changed significantly after water-rock interaction. Finally, a drainage system and sliding force monitoring devices have been arranged at the mine site that can effectively reduce the impact of water-rock interaction on the stability of the mine. This combination of macro-experiments and micro-analysis allowed the weakening effect of dry-wet cycles on slope rock to be studied quantitatively, providing a theoretical reference for stability evaluation in geotechnical engineering.


2020 ◽  
Author(s):  
Marie Haut-Labourdette ◽  
◽  
Daniele Pinti ◽  
André Poirier ◽  
Marion Saby ◽  
...  

2021 ◽  
Vol 3 (7) ◽  
Author(s):  
Otman EL Mountassir ◽  
Mohammed Bahir ◽  
Driss Ouazar ◽  
Abdelghani Chehbouni ◽  
Paula M. Carreira

AbstractThe city of Essaouira is located along the north-west coast of Morocco, where groundwater is the main source of drinking, domestic and agricultural water. In recent decades, the salinity of groundwater has increased, which is why geochemical techniques and environmental isotopes have been used to determine the main sources of groundwater recharge and salinization. The hydrochemical study shows that for the years 1995, 2007, 2016 and 2019, the chemical composition of groundwater in the study area consists of HCO3–Ca–Mg, Cl–Ca–Mg, SO4–Ca and Cl–Na chemical facies. The results show that from 1995 to 2019, electrical conductivity increased and that could be explained by a decrease in annual rainfall in relation to climate change and water–rock interaction processes. Geochemical and environmental isotope data show that the main geochemical mechanisms controlling the hydrochemical evolution of groundwater in the Cenomanian–Turonian aquifer are the water–rock interaction and the cation exchange process. The diagram of δ2H = 8 * δ18O + 10 shows that the isotopic contents are close or above to the Global Meteoric Water Line, which suggests that the aquifer is recharged by precipitation of Atlantic origin. In conclusion, groundwater withdrawal should be well controlled to prevent groundwater salinization and further intrusion of seawater due to the lack of annual groundwater recharge in the Essaouira region.


Author(s):  
Carleton R. Bern ◽  
Justin E. Birdwell ◽  
Aaron M. Jubb

Comparisons of hydrocarbon-produced waters from multiple basins and experiments using multiple shales illustrate water–rock interaction influence on produced water chemistry.


1990 ◽  
Vol 84 (1-4) ◽  
pp. 322-325 ◽  
Author(s):  
C.I. Steefel ◽  
P. Van Capellen ◽  
K.L Nagy ◽  
A.C. Lasaga

2014 ◽  
Vol 78 (6) ◽  
pp. 1473-1477
Author(s):  
Jan Přikryl ◽  
Andri Stefánsson

The interaction of CO2-rich water with olivine was studied using geochemical reaction modelling in order to gain insight into the effects of temperature, acid supply (CO2) and extent of reaction on the secondary mineralogy, water chemistry and mass transfer. Olivine (Fo93) was dissolved at 150 and 250ºC and pCO2 of 2 and 20 bar in a closed system and an open system with secondary minerals allowed to precipitate. The progressive water–rock interaction resulted in increased solution pH, with gradual carbonate formation starting at pH 5 and various Mg-OH and Mg-Si minerals becoming dominant at pH>8. The major factor determining olivine alteration is the pH of the water. In turn, the pH value is determined by acid supply, reaction progress and temperature.


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