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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 65 (1994), S. 3258-3262 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: We have developed a new technique for measuring thermal expansion of liquids at high temperature. Our device, the volumeter, is a volumetric dilatometer which uses liquid tin to transmit volume changes to a series of electrical contacts. Measurements can be carried out from 250 °C to at least 1450 °C irrespective of the viscosity of the sample. In addition, our technique allows for the direct determination of volume changes due to melting and crystallization, as well as the volumetric properties of heterogeneous mixtures of materials. Furthermore, the device is designed to operate inside an internally heated gas-pressured vessel, allowing for the determination of compressibility. We have measured the thermal expansivity of tin from 435 to 1445 °C. Our data match previous measurements using the Archimedean technique to within 4% and shows the volumetric expansivity of tin to have a temperature dependence of −4×10−9 °C−2. Preliminary measurements of the thermal expansivity of a high-viscosity silicate liquid show a wide degree of scatter but fall within previous estimates based on density data. Improved performance of the device may require its operation under pressure.
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemical reviews 91 (1991), S. 1353-1373 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 82 (1999), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Multiple-quantum magic-angle spinning (MQMAS) 17O NMR spectroscopy has been applied to study boron oxide, sodium borate, sodium potassium borosilicate, and sodium boroaluminate glasses. Up to eight distinct oxygen sites are identified, with the chemical shift and quadrupolar coupling parameters determined for each. Previous assignment of the B-O-B and Si-O-B resonances has been found to be incorrect. In contrast to standard models of glass structure, three-coordinated boron mixes with the silicon oxide network to a great extent. Sodium borosilicate glasses with low-sodium content are likely to be phase-separated on the nanoscale. Those with intermediate sodium content form homogeneous glasses with boron atoms distributed evenly in the SiO2 network. A boron avoidance rule analogous to the aluminum avoidance rule may apply in this region, when BO4 groups are abundant. Adding excess sodium cations to the system may again lead to compositional heterogeneity. The existence of diborate group as the basic building unit in glasses with appropriate sodium content is not well supported. The network-forming cations in sodium boroaluminate glasses are well mixed, with no Al-O-Al resonance observed by MQMAS. The effect of cation type and thermal history on glass structures is also discussed.
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 390 (1997), S. 60-62 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The most common of man-made glasses have aluminosilicate compositions, and such glasses also form from rapidly cooling magmas. Oxygen is the most abundant element in these materials, where it occupies either ‘bridging’ (BO) or ‘non-bridging’ (NBO) sites. BOs link two ...
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 351 (1991), S. 638-639 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Pressure-induced changes from SiIV to six-coordinated silicon (Sivl) are well known in crystalline silicates, and most of the silicon in the deep interior of the earth is probably present in the latter state. Data from 29Si magic angle spinning (MAS) NMR confirmed the beginning of this ...
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 330 (1987), S. 465-467 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] For a stoichiometric composition such as Na2Si2O5, the entire glass structure could be made up of a single Q species, as in the crystal (Q3 for this composition). For binary non-stoichiometric compositions, no more than two species are required. The central question is whether a range of species ...
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 20 (1994), S. 587-593 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract We have measured the isotropic chemical shifts (δiso) and the spin-lattice relaxation times (T1) for 17O and 25Mg in MgO from room temperature up to 1300° C. The 17O chemical shifts increase linearly from 47 ppm at room temperature to 57 ppm at 1300° C, and over the same temperature range the 25Mg chemical shift increases linearly from 25 to 27 ppm. These changes are not the result of changes in the bulk magnetic susceptibility of the samples, but may be due to increased orbital overlap which is the result of the increase in thermal vibration of the ions with temperature. In the case of 25Mg, the shift to lower shielding with increasing temperature is opposite to that expected from simple bond length versus chemical shift trends established for the oxides at room temperature. If this is a general phenomenon, high-temperature NMR data may be biased to lower shielding. Spin-lattice relaxation times (T1) were measured in order to study the energetics of defect motion. T1's for 17O and 25Mg exhibit similar behavior over the range of temperatures studied. Up to 800° C, T1's decrease gradually, but above 800° C, T1's drop rapidly, with slopes corresponding to apparent activation energies of 192±9 kJ/mol (2.0±0.1 eV) for 17O and 151±6 kJ/mol (1.56±0.06 eV) for 25Mg. While direct comparison of these activation energies to those derived from diffusion or conductivity measurements is complicated, the similar behavior for both nuclei suggests their relaxation phenomena are related.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 19 (1993), S. 480-485 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Stishovite, a high-pressure SiO2 polymorph in which each Si is coordinated by six O atoms, transforms to an amorphous phase when undergoing heat treatment below the glass transition temperature at ambient pressure. We have applied 29Si magic angle spinning nuclear magnetic resonance spectroscopy (MAS NMR) to study this amorphization process. We found that the amorphous phase generated after heating stishovite for up to 3 days at around 600 ° C consisted exclusively of four-coordinate Si, similar to glasses quenched from melts at ambient pressure. Furthermore, our data suggest that there are subtle structural differences between the amorphous phase transformed from stishovite at 600 ° C and glasses quenched from melts at ambient pressure: the amorphous phase from stishovite had a smaller mean Si-O-Si angle initially, and it gradually relaxed toward the latter with increasing heating time. There was no detectable change in the stishovite structure even after about 80% of it had been converted to the amorphous phase. The mechanism of the amorphization of stishovite is discussed in light of these results.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 20 (1993), S. 297-307 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract In order to decipher information about the local coordination environments of Na in anhydrous silicates from 23Na nuclear magnetic resonance spectroscopy (NMR), we have collected 23Na magic angle spinning (MAS) NMR spectra on several sodium-bearing silicate and aluminosilicate crystals with known structures. These data, together with those from the literature, suggest that the 23Na isotropic chemical shift correlates well with both the Na coordination and the degree of polymerization (characterized by NBO/T) of the material. The presence of a dissimilar network modifier also affects the 23Na isotropic chemical shift. From these relations, we found that the average Na coordinations in sodium silicate and aluminosilicate liquids of a range of compositions at 1 bar are nearly constant at around 6–7. The average Na coordinations in glasses of similar compositions also vary little with Na content (degree of polymerization). However, limited data on ternary alkali silicate and aluminosilicate glasses seem to suggest that the introduction of another network-modifier, such as K or Cs, does cause variations in the average local Na coordination. Thus it appears that the average Na coordination environments in silicate glasses are more sensitive to the presence of other network-modifiers than to the variations in the topology of the silicate tetrahedral network. Further studies on silicate glasses containing mixed cations are necessary to confirm this conclusion.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 16 (1989), S. 763-766 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Dynamics in minerals at time scales from seconds to microseconds are important in understanding mechanisms of displacive phase transitions, diffusion, and conductivity. High resolution, magic-angle-spinning (MAS) NMR spectroscopy can directly show the rates of exchange among sites, potentially providing less model-dependent information than more traditional NMR relaxation time measurements. Here we use a newly developed high temperature MAS probe (Doty Scientific, Inc.) to observe the exchange of Na+ among the alkali sites in a high-Na nepheline at temperatures as high as 500° C. Observed exchange rates are consistent with correlation times derived from cation diffusivity.
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