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  • 1
    Monograph available for loan
    Monograph available for loan
    Washington, D.C. : Mineralogical Society of America
    Associated volumes
    Call number: M 94.0161 / Regal 11
    In: Reviews in mineralogy
    Description / Table of Contents: Fourteen years ago the American Geological Institute (AGI) sponsored a Short Course on Chain Silicates. At that time, a substantial amount was known about the crystal chemistry and phase equilibria of pyroxenes, and this knowledge has been of fundamental importance in guiding research on pyroxenes in the years following the AGI Short Course. In 1966, single-crystal x-ray diffractometry was well advanced and good crystal structure refinements were available for jadeite, spodumene, hypersthene, c1inoferrosi1ite, orthoferrosi1ite, and omphacite; the distinction between the c1inoenstatite (pigeonite) and diopside (augite) structures had been established, and the structure of protoenstatite was known, although some doubt existed about the space group of protoenstatite. Phase diagrams for several joins in the pyroxene quadrilateral had been published, but often equilibrium had not been established in the experiments and not enough was known about the effects of pressure, oxygen fugacity, and non-quad elements such as aluminum on the phase equilibria. Also, inversion relations of Ca-poor pyroxenes were not well understood, and petrologists had just become aware of the effect of stress on orthoto-clinopyroxene transitions. In 1966 few of us would have guessed how-much new data and new analytical results would become available in the next fourteen years. Although most, if not all, of the important instrumental techniques we use today were available in 1966, the truly spectacular development and application of these techniques did not take place until the Apollo 11 samples and the attendant funding from NASA became available. Pyroxene research has profited immensely from the application of Mossbauer, optical, and infrared spectroscopy, x-ray and electron diffraction, transmission electron microscopy, automated electron microprobes, and digital computers. During these years experimentalists extended the capabilities of their equipment to examine the behavior of pyroxenes under conditions of controlled oxygen fugacity, pressure, and temperature, conditions more nearly like those under which pyroxenes crystallize in natural systems. Looking back, one remembers the excitement of seeing the first lunar samples. We were surprised at the large amounts of pigeonite and the quality of crystals unaffected by water or the presence of sodium. The influence of the lunar program on pyroxene research was extraordinary, and our understanding of pyroxene relationships in terrestrial occurrences benefited tremendously because the lunar pyroxenes provided a basis for comparison with the more complex chemical and structural behavior of terrestrial environments. Probably the most impressive development in the early lunar sample studies was the application of transmission electron microscopy to mineralogy. We were able to see exsolution and other textural features in crystals that looked homogeneous in the optical microscope, thus opening up a wide range of research possibilities that had not existed previously. Advanced crystal growth experiments, detailed phase equilibria, x-ray diffraction at high temperatures, and statistical analyses of microprobe data were all applied to lunar pyroxenes and then extended to terrestrial and meteorite investigations, making this period one of the most productive in history. In the compilation of this volume, an attempt has been made to review the essential aspects of pyroxene research, primarily those of the last ten or fifteen years. Although the largest fraction of pyroxene research has been performed in the U.S.A., significant advances have been made in other countries, particularly in Europe, Japan, Canada, and Australia, with interest and activity in these countries probably growing at a faster rate than in the United States. Recently, Deer, Howie and Zussman (DHZ) published a second edition of their volume in the Rock-Forming Minerals series, Single-Chain Silicates, Vol. 2A (John Wiley, New York, 1978). The present volume is intended to be complementary to DHZ and to provide material covered lightly or not at all in DHZ, such as electron microscopy, spectroscopy, and detailed thermodynamic treatments. However, because the range of pyroxene research has grown so much in recent years, there still are important areas not covered comprehensively in either of these volumes. Some of these areas are kinetics, diffusion, crystal defects, deformation, and nonsilicate pyroxene crystal chemistry. Because of these omissions and because this volume is intended for use with the MSA Short Course on Pyroxenes to be held at Emory University in conjunction with the November, 1980 meeting of the Society, a Symposium on Pyroxenes was organized by J. Stephen Huebner for the meeting that is designed to present the latest research results on several different topics, including those above. With DHZ, this volume, and publications from the Symposium, the student of pyroxenes should be well-equipped to advance our knowledge of pyroxenes in the decades ahead.
    Type of Medium: Monograph available for loan
    Pages: x, 525 S.
    Edition: 2nd print.
    ISBN: 0-939950-07-3 , 978-0-939950-07-2
    ISSN: 1529-6466
    Series Statement: Reviews in mineralogy 7
    Classification:
    Mineralogy
    Language: English
    Note: Chapter 1. Introduction by Charles T. Prewitt, p. 1 - 4 Chapter 2. Crystal Chemistry of Silicate Pyroxenes by Maryellen Cameron and James J. Papike, p. 5 - 92 Chapter 3. Pyroxene Spectroscopy by George R. Rossman, p. 93 - 116 Chapter 4. Subsolidus Phenomena in Pyroxene by Peter R. Buseck, Gordon L. Nord, Jr., and David R. Veblen, p. 117 - 212 Chapter 5. Pyroxene Phase Equilibria at Low Pressure by J. Stephen Huebner, p. 213 - 288 Chapter 6. Phase Equilibria of Pyroxenes at Pressure 〉1 Atmosphere by Donald H. Lindsley, p. 289 - 308 Chapter 7. Phase Equilibria at High Pressure of Pyroxenes Containing Monovalent and Trivalent Ions by Tibor Gasparik and Donald H. Lindsley, p. 309 - 340 Chapter 8. Thermodynamics of Pyroxenes by J. E. Grover, p. 341 - 418 Chapter 9. The Composition Space of Terrestrial Pyroxenes - Internal and External Limits by Peter Robinson, p. 419 - 494 Chapter 10. Pyroxene Mineralogy of the Moon and Meteorites by James J. Papike, p. 495 - 525
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  • 2
    Call number: 11/M 94.0644
    In: Reviews in mineralogy
    Description / Table of Contents: Oxygen and silicon are the two most common elements in the earth's crust, together constituting an estimated 74.32 weight % and 83.77 atom % of crustal rocks (Mason and Moore, 1982). Thus, it is not surprising that SiO2 or silica, is the most abundant oxide on the earth's surface. In his widely cited survey, Clarke (1904) calculated that quartz alone comprises 12.0% of the crust by volume, ranking behind the mineral groups that include feldspar (59.5%) and amphibole/pyroxene (16.8%). Consequently, research into the silica system is motivated foremost by the prevalence of silica in man's immediate environment. The ubiquity of silica in igneous, metamorphic, and sedimentary rocks has led earth scientists to seek its uses as an indicator of large-scale geological processes, ranging from mountain-building to meteorite impacts. In industry, quartz has long played a prosaic but essential role as an inexpensive and relatively inert constituent of concrete aggregates, and modern electronics technology still relies on quartz oscillators. Silica phases also have played a prominent role in our understanding of the solid state. Physicists first discovered optical activity in crystals and the existence of soft modes during their investigations of quartz. Many scientists have written substantial reviews documenting the importance of silica in the earth, materials, and physical sciences. Notable among these are Robert Sosman, who followed his Properties of Silica (1927) with The Phases of Silica (1965), and Clifford Frondel, who devoted the third volume of Dana's System of Mineralogy (1962) exclusively to the silica minerals. These treatises continue to serve as encyclopedic resources for those interested in silica, and their historical analyses and descriptions of mineral varieties, morphologies, and localities will remain forever useful. Nevertheless, the past three decades have witnessed a first-order expansion of our knowledge of the silica system, and it is time to provide an updated silica review. The present volume focuses on the most recent developments, and it is intended to supplement rather than replace the earlier works of Sosman and Frondel. The contributions to this volume cover silica chemistry in the following fashion: Chapters 1 through 3 describe the crystal structures and phase transitions of silica and its stuffed derivatives. Recent studies of the low-pressure polymorphs quartz, tridymite, and cristobalite have demonstrated unusual superperiodic phases and other anomalies associated with structural transformations (Chapter 1). Spectacular progress in multianvil and diamond cell technologies has made the high-pressure regime accessible, revealing new transitions in the coesite and stishovite systems as well as the phenomenon of pressureinduced amorphization (Chapter 2). Stoichiometric substitution of cations within the frameworks of both low- and high-pressure polymorphs produces a dizzying variety of derivative compounds that are of geological and industrial importance (Chapter 3). Chapters 4 through 9 bridge the relationship between the microstructural character of real silica minerals and the behavior of silica in the geological environment. Incorporation of small amounts of H dramatically weakens quartz exposed to stress (Chapter 4). Consequently, tectonic pressures may lead not to brittle fracture but to the production of high densities of dislocations and preferred orientation in polycrystalline quartz (Chapter 5). The low pressures and temperatures in sedimentary settings may promote the crystallization of highly defective silica phases that are frequently metastable (Chapter 6); through diagenetic processes, these minerals anneal to macrocrystalline quartz (Chapter 7). The nature of the surface structure of quartz strongly influences the mechanisms and kinetics of silica dissolution in aqueous fluids (Chapter 8). Chapters 9 through 13 treat the basic physical properties of the phases of silica. Recent calorimetric studies of some of the more unusual silica compounds have added insight into the stability of the silica framework (Chapter 9). Quantum mechanical considerations of the Si-O bond have yielded a fundamental understanding of the bond lengths and angles within the polymorphous silica system (Chapter 10). Calculations based upon first-principles theory have achieved significant success in explaining and predicting silica transitions at high temperatures and pressures (Chapter 11). Spectroscopic analyses of silica (Chapters 12 and 13) have revealed vibrational behaviors in response to variations in temperature, pressure, and composition that have deepened our understanding of the dynamic interactions within the silica structure. Chapters 14 through 16 detail the uses of silica for industrial purposes. For instance, doping silica with other cations produces ceramics with low expansion on heating (Chapter 14), and high-silica zeolites are being explored for their properties as catalysts and molecular sieves (Chapter 15). High concentrations of silica dust in the workplace long have been linked with the incidence of respiratory diseases, such as silicosis, and recent evidence suggests that crystalline silica may be carcinogenic (Chapter 16).
    Type of Medium: Monograph available for loan
    Pages: xviii, 606 S.
    ISBN: 0-939950-35-9 , 978-0-939950-35-5
    ISSN: 1529-6466
    Series Statement: Reviews in mineralogy 29
    Classification:
    Mineralogy
    Language: English
    Note: CRYSTAL CHEMISTRY OF SILICA AND ITS STUFFED DERIVATIVES Chapter 1. Structure and Chemistry of the Low-Pressure Silica Polymorphs by Peter J. Heaney, p. 1 - 40 Chapter 2. High-Pressure Behavior of Silica by Russell J. Hemley, Charles T. Prewitt, and Kathleen J. Kingma, p. 41 - 82 Chapter 3. Stuffed Derivatives of the Silica Polymorphs by David C. Palmer, p. 83 - 122 SILICA in the GEOLOGICAL ENVIRONMENT Chapter 4. Hydrogen Speciation and Chemical Weakening of Quartz by Andreas A. Kronenberg, p. 123 - 176 Chapter 5. Preferred Orientation Patterns in Deformed Quartzites by Hans-Rudolf Wenk, p. 177 - 208 Chapter 6. Structural Characteristics of Opaline and Microcrystalline Silica Minerals by Heribert Graetsch, p. 209 - 232 Chapter 7. Petrogenesis of Chert by L. Paul Knauth, p. 233 - 258 Chapter 8. Silica-Water Interactions by Patricia M. Dove and J. Donald Rimstidt, p. 259 - 308 PHYSICAL BEHAVIOR of SILICA Chapter 9. Thermochemistry of Crystalline and Amorphous Silica by Alexandra Navrotsky, p. 309 - 330 Chapter 10. The Elusive SiO Bond by Gerald V. Gibbs, James W. Downs, and Monte B. Boisen Jr., p. 331 - 368 Chapter 11. First-Principles Theory of Crystalline SiO2 by Ronald E. Cohen, p. 369 - 402 Chapter 12. Lattice Dynamical Behavior of Anhydrous Silica by Gerard Dolino and Marcel Vallade, p. 403 - 432 Chapter 13. Colored Varieties of the Silica Minerals by George R. Rossman, p. 433 - 468 SILICA as an INDUSTRIAL MATERIAL Chapter 14. Industrial Applications of Silica by George H. Beall, p. 469 - 506 Chapter 15. Silica Zeolites and Clathrasils by John B. Higgins, p. 507 - 544 Chapter 16. Health Effects of Silica Dust Exposure by David F. Goldsmith, p. 545 - 606
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 8 (1969), S. 1985-1993 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 7 (1968), S. 1090-1093 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 7 (1968), S. 2282-2288 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 10 (1971), S. 713-718 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 4 (1979), S. 105-113 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The thirteen single-crystal elastic moduli for diopside as determined by the acoustic technique based on Brillouin scattering are: c11=2.23, c22=1.71, c33=2.35, c44=0.74, c55=0.67, c66=0.66, c12=0.77, c13=0.81, c15=0.17, c23=0.57, c25=0.07, c35=0.43, c46=0.073. The Reuss bound of the adiabatic bulk and shear moduli calculated from these data are K s=1.08 Mbar and G=0.651 Mbar. The room-pressure isothermal bulk modulus, K T , and the pressure derivative of the bulk modulus, K′ T have also been determined on a four-circle diffractometer, from a single crystal mounted in a gasketed opposed-anvil diamond cell, giving values of K T =1.13 Mbar and K′ T =4.8. The principal axes of the strain ellipsoid, calculated from the elastic moduli and observed in the static compression data, are identical, and the linear compressibilities are in reasonable agreement. The single-crystal elastic moduli can be correlated with the structural features of diopside.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 16 (1989), S. 621-629 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The stable polymorph of MnTiO3 at room temperature and pressure has the ilmenite structure. At high temperatures and pressures, MnTiO3 ilmenite transforms to a LiNbO3 structure through a cation reordering process (Ko and Prewitt 1988). Single crystals of both phases have been studied with X-ray diffraction to 5.0 GPa. We have obtained the first experimental verification of the close relationship between the LiNbO3 and perovskite structures, first postulated by Megaw (1968). MnTiO3 with the LiNbO3 structure (MnTiO3 II) transforms directly to an orthorhombic perovskite structure (MnTiO3 III) between 2.0 and 3.0 GPa. The transition involves a change of volume of -5%, is reversible and has pronounced hysteresis. Only pressure is required to drive the transition because it involves no breaking of bonds; it simply involves rotation of the [TiO6] octahedra about their triad axes accompanied by displacement of the Mn cations to the distorted twelve-coordinated sites formed by the rotations. An unusual aspect of this transition is that twinned MnTiO3 II crystals transform to untwinned MnTiO3 III crystals with increasing pressure. The twin plane of MnTiO3 II, $$\left( {10\bar 1\bar 2} \right)$$ , corresponds to the (001) mirror plane of the orthorhombic perovskite structure. MnTiO3 III examined at 4.5 GPa is very distorted from the ideal cubic perovskite structure. The O(2)-O(2)-O(2) angle describing the tilting in the ab plane is 133.3(7)°, in contrast to 180° for a cubic perovskite and the O(2)-O(2)-O(2) angle describing the tilting in the ac plane is 109.3(4)°, as opposed to 90° in a cubic perovskite.
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