Hydrogen diffusion mechanisms in quartz: insights from H–Li, <sup>2</sup>H–H and <sup>2</sup>H–H–Li exchange experiments

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Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_988C498EBDF9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Hydrogen diffusion mechanisms in quartz: insights from H–Li, <sup>2</sup>H–H and <sup>2</sup>H–H–Li exchange experiments
Périodique
Mineralogical Magazine
Auteur⸱e⸱s
Jollands Michael C., Tollan Peter M. E., Baumgartner Lukas P., Müntener Othmar
ISSN
0026-461X
1471-8022
Statut éditorial
Publié
Date de publication
02/2022
Peer-reviewed
Oui
Volume
86
Numéro
1
Pages
112-126
Langue
anglais
Résumé
The diffusivity and diffusion mechanisms of hydrogen together with with deuterium and lithium, parallel to the c axis of quartz, were investigated experimentally at 800°C, 0.1 GPa with the activity of H2O or 2H2O ≈ 1 [2H is used throughout this work to describe deuterium rather than D, to avoid confusion with the diffusion coefficient, D]. The pH was set using mixtures of H2O (or 2H2O) and HCl. Three types of experiment were conducted: (1) H-in/Li-out; (2) 2H-in/H-out; and (3) 2H-in/H + Li out, using three different natural quartz crystals as starting materials. Profiles of H, 2H and Li were measured using Fourier-transform infrared (FTIR) spectroscopy and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). H, 2H and Li are charge-compensated by Al3+ replacing Si4+, or by excess O2–. The total atomic concentration of monovalent cations appears to remain constant over the duration of the experiments. The resulting diffusion profiles are different for the three experimental designs and three starting materials, and some show complex shapes inconsistent with simple diffusion. A multi-site diffusion–reaction model is developed, with the theory based on previous models that have been derived mainly on the basis of conductivity measurements. In these models, the monovalent cations move away from their charge-balancing ion then diffuse rapidly to another site. The mobility of the monovalent cations is described by both a diffusion coefficient and an equilibrium constant that enables dissociation of the immobile charge-balanced defects. This model can describe complex step-shaped profiles formed in H-in/Li-out experiments, profiles with local maxima ('humped’ profiles) in 2H-in/H + Li out experiments, and error function-shaped profiles in 2H-in/H-out and previously published Li-in/H-out experiments. Our data provide support for models previously proposed for quartz. Studies of the lengths and forms of diffusion profiles from such experiments provide a useful complement to assertions from conductivity experiments.
Mots-clé
quartz, diffusion, Fourier transform infrared spectroscopy, point defects
Web of science
Open Access
Oui
Création de la notice
08/04/2022 14:47
Dernière modification de la notice
22/02/2023 8:13
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