Reaction-Transport Models for Radiocarbon in Groundwater: The Effects of Longitudinal Dispersion and the use of Sr Isotope Ratios to Correct for Water-Rock Interaction

1996 ◽  
Vol 32 (7) ◽  
pp. 2203-2212 ◽  
Author(s):  
T. M. Johnson ◽  
D. J. DePaolo
Keyword(s):  
Isotope Ratios ◽  
Longitudinal Dispersion ◽  
Sr Isotope ◽  
Transport Models ◽  
Rock Interaction ◽  
Reaction Transport ◽  
Water Rock Interaction

scholarly journals The calculation of water-rock ratios using trace element (Li, B) stable isotopes

2017 ◽  
Vol 71 ◽  
pp. 79
Author(s):  
Laurent Simon ◽  
Christophe Lécuyer ◽  
Thibaut Putelat
Keyword(s):  
Mass Balance ◽  
Isotopic Exchange ◽  
Open Systems ◽  
Elemental Distribution ◽  
Sr Isotope ◽  
Balance Equations ◽  
Rock Interaction ◽  
Circulating Water ◽  
Li Isotope ◽  
Water Rock Interaction

The amount of aqueous fluids circulating into the oceanic crust can be estimated using mass balance equations based on stable isotope exchange between rock and water. Unlike oxygen and strontium, isotopic exchange of trace elements (such as B or Li) between fluids and rocks, operates along with a chemical evolution of the rocks (e.g. a large enrichment of B or Li) that must be integrated into any model of water-rock interaction. We propose a general dimensionless mass balance equation for single-pass open systems that describes the equilibrium elemental distribution and the isotopic composition of reacting rocks as a function of the amount of circulating water. Water-rock ratios calculated from B compositions of hydrothermally-altered basalts range from 8 to 100. They are lower than those previously published (most W/R > 300) but comparable to those inferred from Sr isotope ratios measured in the same samples (3 < W/R < 30). Similar low water-rock ratios from 2 to 20 are calculated from Li isotope compositions of altered basalts and serpentinized peridotites.

TRACING MOISTURE SOURCES OF THE EXTREME STORM EVENT IMPACTING THE CAROLINAS IN OCTOBER, 2015 USING O, H, AND SR ISOTOPE RATIOS

2016 ◽  
Author(s):  
Donna Surge ◽  
◽  
Karly R. Schmidt ◽  
Corey Moore ◽  
Drew S. Coleman ◽  
...  
Keyword(s):  
Isotope Ratios ◽  
Storm Event ◽  
Sr Isotope ◽  
Moisture Sources ◽  
Extreme Storm

87SR/86SR, δ18O AND NOBLE GASES AS TRACERS OF WATER-ROCK INTERACTION IN THE THEISTAREYKIR GEOTHERMAL FIELD

2020 ◽  
Author(s):  
Marie Haut-Labourdette ◽  
◽  
Daniele Pinti ◽  
André Poirier ◽  
Marion Saby ◽  
...  
Keyword(s):  
Noble Gases ◽  
Geothermal Field ◽  
Rock Interaction ◽  
Water Rock Interaction

scholarly journals Geochemical and isotopic evidence of groundwater salinization processes in the Essaouira region, north-west coast, Morocco

2021 ◽  
Vol 3 (7) ◽  
Author(s):  
Otman EL Mountassir ◽  
Mohammed Bahir ◽  
Driss Ouazar ◽  
Abdelghani Chehbouni ◽  
Paula M. Carreira
Keyword(s):  
Groundwater Recharge ◽  
West Coast ◽  
Exchange Process ◽  
Environmental Isotopes ◽  
Annual Rainfall ◽  
Groundwater Salinization ◽  
Rock Interaction ◽  
North West ◽  
The North ◽  
Water Rock Interaction

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.

scholarly journals Water–rock interaction and the concentrations of major, trace, and rare earth elements in hydrocarbon-associated produced waters of the United States

2021 ◽  
Author(s):  
Carleton R. Bern ◽  
Justin E. Birdwell ◽  
Aaron M. Jubb
Keyword(s):  
United States ◽  
Rare Earth ◽  
Rare Earth Elements ◽  
Water Chemistry ◽  
Produced Water ◽  
The United States ◽  
Rock Interaction ◽  
Produced Waters ◽  
Water Rock Interaction

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

Modeling water-rock interaction in the surficial environment: The role of precursors, nucleation, and Ostwald ripening

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

scholarly journals CO2 mineralization by olivine at hydrothermal conditions

2014 ◽  
Vol 78 (6) ◽  
pp. 1473-1477
Author(s):  
Jan Přikryl ◽  
Andri Stefánsson
Keyword(s):  
Ph Value ◽  
Hydrothermal Conditions ◽  
Solution Ph ◽  
Rock Interaction ◽  
Carbonate Formation ◽  
Effects Of Temperature ◽  
Co2 Mineralization ◽  
Geochemical Reaction ◽  
Insight Into ◽  
Water Rock Interaction

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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