Strontium isotope fractionation during precipitation of strontianite in aqueous solutions as a function of temperature and reaction rate

dc.contributor.authorAlkhatib, Mahmoud
dc.contributor.authorQutob, Mutaz
dc.contributor.authorAlkhatib, Samia
dc.contributor.authorEisenhauer, Anton
dc.date.accessioned2021-12-18T12:11:46Z
dc.date.available2021-12-18T12:11:46Z
dc.date.issued2021-11-07
dc.description.abstractIn order to study Strontium (Sr) isotope fractionation during the precipitation of strontianite (SrCO3) as a function of the specific precipitation rate (R*) and temperature (T), strontianite was precipitated at 12.5, 25.0 and 37.5 ◦C by diffusing NH3 and CO2 gases into aqueous solutions. The specific precipitation rate R* (mol/ cm2.h) for every sample was determined by applying the initial rate method. The mean isotope difference be- tween bulk solution and precipitate (∆88/86Srstrontianite-solution) was found to be − 0.279 ± 0.005‰ (2σmean) in- dependent of both rate and temperature. Hence, Sr isotope fractionation in strontianite is completely different from that in calcite and aragonite, where a strong dependency from both rate and temperature can be observed. The latter is interpreted to reflect the competition between Sr2+ and Ca2+ ions for incorporation into the calcium carbonate crystal lattice, which is absent during the precipitation of pure strontianite. The isotope difference between strontianite and bulk solution then simply reflects the intermolecular forces in the aqueous solutions as well as the kinetic effect. The difference in the (∆88/86Srstrontianite-solution between experiments then reflects the dehydration energy of Sr ions in the adsorption layer of SrCO3.en_US
dc.identifier.issn0009-2541
dc.identifier.urihttps://dspace.alquds.edu/handle/20.500.12213/6496
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectStrontium isotopeen_US
dc.subjectFractionationen_US
dc.subjectStrontianite precipitationen_US
dc.titleStrontium isotope fractionation during precipitation of strontianite in aqueous solutions as a function of temperature and reaction rateen_US
dc.typeArticleen_US
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