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Kinetics of the reaction H_2O+O=2OH in rhyolitic and albitic glasses: Preliminary results

Zhang, Youxue and Stolper, E. M. and Ihinger, P. D. (1995) Kinetics of the reaction H_2O+O=2OH in rhyolitic and albitic glasses: Preliminary results. American Mineralogist, 80 (5-6). pp. 593-612. ISSN 0003-004X. https://resolver.caltech.edu/CaltechAUTHORS:20120827-121639823

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Abstract

The kinetics of homogeneous reactions are important in understanding the cooling history of rocks and in understanding experimental speciation data. We have experimentally studied the kinetics of the interconversion reaction between H_2O molecules and OH groups in natural rhyolitic glasses (0.5-2.3% total water) and a synthetic albitic glass (l% total water) at 400-600°C. The reaction rate increases with temperature and total water content. Equilibrium is not always approached monotonically; the speciation may first depart from equilibrium and then come back to equilibrium. Experimental reaction rates agree with those inferred from previous speciation data of rhyolitic glasses quenched from 850°C. The experimental data are modeled successfully by considering both the reaction and the diffusion of OH that brings OH groups together to react. This study shows that species concentrations in glasses quenched from ≤ 600°C reflect those at experimental temperatures unless the water content is higher than that used in the present study. Species concentrations in glasses with total water contents ≥0.8 wt% and which were rapidly quenched in water from 850°C do not represent their equilibrium concentrations in the melt at 850°C, but record a lower apparent equilibrium temperature that depends on water content and quench rate. Natural rhyolitic glasses and glass inclusions do not record preeruptive melt speciation, though total water content may be conserved. The experimental data are used to infer cooling rates for natural obsidian glasses. Pyroclastic glass fragments from the bb site of Mono Craters have cooling rates similar to air-cooled experimental charges (~3°C/s). Different types of glasses from the Mono Craters have different cooling rates, which cover four orders of magnitude. Some natural obsidians appear to have had complex cooling histories. The wide range of cooling rates and thermal histories is consistent with previous inferences that some obsidian clasts at the Mono Craters formed as glass selvages lining volcanic conduits or dikes that were subsequently caught up in the explosive eruption, which led to variable degrees of transient heating followed by rapid cooling and deposition. These experimental data reveal surprisingly rich detail in water speciation in volcanic glasses and show how, at least in principle, quantitative constraints on thermal histories can be extracted by experimentation and application of kinetic models.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://www.minsocam.org/MSA/AmMin/TOC/1995/MJ95.htmlPublisherArticle
ORCID:
AuthorORCID
Zhang, Youxue0000-0002-7439-0086
Stolper, E. M.0000-0001-8008-8804
Additional Information:© 1995 Mineralogical Society of America. Manuscript received April 7, 1994; Manuscript accepted January 23, 1995. Discussions with G.R Gavalas (of California Institute of Technology), A.C Lasaga, and S. Newman have been most helpful. Comments by D.B. Dingwell, E.J. Essene, RA. Lange, H.N. Pollack, E.B. Watson, B.H. Wilkinson, and an anonymous reviewer are appreciated. Y.Z. thanks J.G. Blank and P.F. Dobson for their help in collecting some of the samples from the "bb" site used in this study, and R. Belcher for some FTIR analyses. This work was supported by NSF grants EAR-8916707, EAR-9219899, EAR-9304161, and EAR-9315918 and DOE grant DE-FG03-85ER13445. Division of Geological and Planetary Sciences Contribution no. 5386.
Funders:
Funding AgencyGrant Number
NSFEAR-8916707
NSFEAR-9219899
NSFEAR-9304161
NSFEAR-9315918
Department of Energy (DOE)DE-FG03-85ER13445
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Caltech Division of Geological and Planetary Sciences5386
Issue or Number:5-6
Record Number:CaltechAUTHORS:20120827-121639823
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20120827-121639823
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ID Code:33566
Collection:CaltechAUTHORS
Deposited By:INVALID USER
Deposited On:27 Aug 2012 20:33
Last Modified:27 Nov 2019 18:16

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