Abstract

CO(2)-rich solutions are common in geological environments. An XANES (X-ray absorption near-edge structure) study of Br in CO(2)-bearing synthetic fluid inclusions has revealed that Br exhibits a strong pre-edge feature at temperatures from 298 to 423 K. Br in CO(2)-free solutions does not show such a feature. The feature becomes smaller and disappears as temperature increases, but reappears when temperature is reduced. The size of the feature increases with increasing X(CO(2)) in the fluid inclusion, where X(CO(2)) is the mole fraction of CO(2) in the solution [n(CO(2))/(n(CO(2)) + n(H(2)(O)) + n(RbBr)); n indicates the number of moles]. The pre-edge feature is similar to that shown by covalently bonded Br, but observed and calculated concentrations of plausible Br-bearing covalent compounds (Br(2), CH(3)Br and HBr) are vanishingly small. An alternative possibility is that CO(2) affects the hydration of Br sufficiently that the charge density changes to favour the 1s-p level transitions that are thought to cause the pre-edge peak. The distance between the first two post-edge maxima in the XANES also decreases with increasing X(CO(2)). This is attributed to a CO(2)-related decrease in the polarity of the solvent. The proposed causes of the observed features are not integrated into existing geochemical models; thus CO(2)-bearing solutions could be predicted poorly by such models, with significant consequences for models of geological processes such as ore-formation and metamorphism.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.