Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
American Mineralogist Signup for GSW Email News
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

American Mineralogist; October; v. 93; no. 10; p. 1620-1629; DOI: 10.2138/am.2008.2821
© 2008 Mineralogical Society of America
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Branlund, J. M.
Right arrow Articles by Hofmeister, A. M.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

Factors affecting heat transfer in natural SiO2 solids

Joy M. Branlund* and Anne M. Hofmeister

Department of Earth and Planetary Sciences, Washington University in St. Louis, 1 Brookings Drive, St. Louis, Missouri 63130-4899, U.S.A.

To determine which factors affect thermal diffusivity (D) of mineral aggregates, we compared accurate measurements of D for five quartzites, two microcrystalline samples (chert and agate), chalcedony, and two partially crystalline opal specimens (of type opal-CT) with single-crystal quartz. Samples were characterized using infrared (IR) spectroscopy, electron microprobe analysis, optical microscopy, and X-ray powder diffractometry (XRD). Using laser flash analysis, we measured D of the quartzites and microcrystalline samples between room temperature and 1000 °C, and D of the opal specimens and chalcedony up to the temperatures where these samples failed (300 and 650 °C, respectively). Data between 20 and 500 °C can be fit by 1/D = AT + B. Values of A and B for quartzites, microcrystalline samples, opal specimens, and chalcedony are distinct from each other and from those of directionally averaged quartz single-crystals. Lower D at room temperature correlates with inflated B values of polycrystalline samples and results from porosity (all samples), hydration (all samples), grain boundaries (microcrystalline samples and chalcedony), and disorder (opal specimens and chalcedony). Dehydration and pore space reduction alter the temperature derivatives of D; dehydration causes the low A in chalcedony and opal. Above 600 °C, D changes negligibly with temperature and is lower than directionally averaged quartz, suggesting an increase in contact resistance as cracks open during heating. Thermal cracking is greatest in samples with large grain sizes and abundant, fluid-filled pores. The prevalence of cracking in polycrystalline samples suggests that high-temperature laboratory measurements generally underestimate heat transport properties in geologic environments, wherein confining pressures limit thermal expansion.

Key Words: Quartzite • silica • thermal diffusivity • laser flash analysis • porosity • grain size • temperature







JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Mineralogical Society of America