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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 6 (1967), S. 2119-2121 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 7 (1995), S. 1816-1823 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 5 (1993), S. 1805-1813 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 8 (1969), S. 756-758 
    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
    Springer
    Pure and applied geophysics 141 (1993), S. 615-629 
    ISSN: 1420-9136
    Keywords: Experimental techniques ; calorimetry ; high-pressure ; mineral physics ; phase transitions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract We have designed and calibrated a piston-cylinder cell assembly suitable for conductingin situ measurements of enthalpies of phase transitions at elevated pressures by heat-flux differential scanning calorimetry (DSC). The high-pressure DSC detector consists of a Pt-Pt13%Rh thermopile wrapped around a frame of fired pyrophyllite. Four thermocouple junctions, arranged radially around the sample capsule, are connected in series, with four reference thermocouple junctions located 3–4 mm above the sample and embedded in thermally inert ceramic. A W-W25%Re control thermocouple is situated directly above the top of the sample; the whole detector assembly is enclosed in a 1.5 mm thick cylindrical ceramic sleeve located at the center of a 8–10 mm long “hot-zone” in the tapered graphite furnace. Using this detector design and cell assembly, we have observed the thermal signal associated with the fusion of Au at 0.5 and 1.2 GPa, and have calculated a calibration factor (K) for this detector based on the gold melting curve ofMirwald andKennedy (1979). Detector sensitivity decreases by a factor of four over this pressure-temperature interval. The reproducibility of the enthalpy of fusion of gold at 0.5 GPa suggests that detector geometry is reproducible from one experiment to the next, and thus confirms the viability of this particular detector design for quantitative DSC measurements. Subsequent experiments will assess the dependence of (K) on temperature and pressure by measuring the enthalpies of fusion of additional metals (e.g., Ag, Cu, Al, Ge) and salts (e.g., NaCl, CsCl).
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillian Magazines Ltd.
    Nature 408 (2000), S. 844-847 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] During the subduction of oceanic lithosphere, water is liberated from minerals by progressive dehydration reactions and is thought to be critical to several geologically important processes such as island-arc volcanism, intermediate-depth seismicity and chemical exchange between the subducting ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 87 (2004), 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: The relative partial molar enthalpies, ΔH̄SiO2, of SiO2 in SiO2–M2O (M = Li, Na, K and Cs) binary and SiO2–CaO–Al2O3ternary melts were directly measured by drop-solution calorimetry at 1465 K and 1663 K. ΔH̄SiO2 changes from exothermic to endothermic as silica content increases, confirming the tendency toward immisciblity seen from activity measurements. It is concluded that ΔH̄SiO2 is negative due to acid-base reactions and charge-coupled substitutions when the melt is composed of fewer Q4 and more Q3 and Q2 species, but positive due to structural strain when the melt is composed of mostly Q4 species. The ΔH̄SiO2 obtained by calorimetry is a useful measure of basicity, when comparing different alkali and alkaline earth oxides.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 85 (2002), 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: The crystal structures for a suite of substituted pollucites with the compositions CsTixAl1–xSi2O6+0.5x, 0 ≤x≤ 1, have been determined from Rietveld analysis of powder synchrotron XRD data. Our results indicate that the pollucite end member (CsAlSi2O6) has a tetragonal structure (space group I41/a), whereas all other compositions are cubic (space group Ia3d). The increased symmetry for the titanium-substituted structures is presumably due to the incorporation of additional O2− anions (needed for compensating the charge imbalance between Ti4+ and Al3+), which effectively holds open the expanded cubic framework. In situ cooling experiments of the substituted phase CsTi0.1Al0.9Si2O6.05 reveal a displacive transformation to the tetragonal structure at ∼230 K. This transformation is tricritical in nature and is analogous to the tetragonal-to-cubic transition in pollucite on heating.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 85 (2002), 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: Thermodynamics of the Na1−xLixNbO3 system is investigated by high-temperature drop-solution calorimetry in molten 3Na2O–4MoO3 solvent at 973 K. Standard molar enthalpies of formation are derived. The estimated heats of transition between hypothetical and stable structures, lithium niobate and perovskite for NaNbO3 and vice versa for LiNbO3 are −6 kJ/mol and −10 kJ/mol, respectively. X-ray diffraction studies at room temperature showed for 0 ≤x≤ 0.14 there are three phases based on different ordering of the perovskite type lattice: orthorhombic with a quadrupled reduced perovskite cell at 0 ≤x≤ 0.02, orthorhombic with a doubled reduced perovskite cell at 0.015 ≤x≤ 0.14, and rhombohedral at 0.08 ≤x≤ 0.13. There are two two-phase (morphotropic) regions with coexistence of the two orthorhombic phases at 0.015 ≤x≤ 0.02 and with the second orthorhombic phase coexisting with the rhombohedral phase at 0.08 ≤x≤ 0.13. A reproducible anomaly in specific heat at ∼600 K, not reported previously, has been observed in pure NaNbO3. Heat-capacity measurements confirm a phase transition at 553 K for 0.07 ≤x≤ 0.09. With increasing lithium concentration, a gradual disappearance of high-temperature phase transitions associated with tilting of oxygen octahedra has been observed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    Journal of the American Ceramic Society 88 (2005), 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: High-temperature differential thermal analysis provided data on phase transitions in zirconia and yttria. The tetragonal form of ZrO2 transforms to the cubic fluorite structure at 2311°±15°C with an enthalpy of 3.4±3.1 kJ/mol. Cubic C-type Y2O3 transforms, probably to the fluorite structure, at 2308°±15°C with ΔH=47.7±3.0 kJ/mol. This high-temperature polymorph melts at 2382°±15°C with an enthalpy of fusion of 35.6±3.0 kJ/mol.
    Type of Medium: Electronic Resource
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