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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Inorganica Chimica Acta 181 (1991), S. 201-205 
    ISSN: 0020-1693
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Applications of Surface Science 2 (1979), S. 335-351 
    ISSN: 0378-5963
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Micron (1969) 13 (1982), S. 267-268 
    ISSN: 0047-7206
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Micron (1969) 11 (1980), S. 321-322 
    ISSN: 0047-7206
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 11 (2000), S. 691-696 
    ISSN: 1573-482X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The present work reports equilibration kinetics for (La0.8,Sr0.2)CoO3(LSC) and (La0.72,Sr0.18)FeO3(LSF) in the temperature range 876–1114 K using a gravimetric method. Chemical diffusion determined in this way that depends on oxygen partial pressure, can be expressed by the following temperature dependence at low and high O2), respectively, for LSC: $$D_{chem} = 8.7 \times 10^{ - 3} {\text{exp}}\frac{{{\text{ - }}\left( {58.1 \pm 8.5} \right){\text{kJ/mol}}}}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (1)}}$$ $$D_{chem} = 6.2 \times 10^{ - 3} {\text{exp}}\frac{{{\text{ - }}\left( {75.4 \pm 6.5} \right){\text{kJ/mol}}}}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (2)}}$$ and for LSF: $$D_{chem} = 3.05 \times 10^{ - 5} {\text{exp}}\frac{{{\text{ - }}\left( {30.3 \pm 2.8} \right){\text{kJ/mol}}}}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (3)}}$$ $$D_{chem} = 6.3 \times 10^{ - 3} {\text{exp}}\frac{{{\text{ - }}\left( {82.7 \pm 10.2} \right){\text{kJ/mol}}}}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (4)}}$$
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 11 (2000), S. 697-702 
    ISSN: 1573-482X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The present work reports isothermal changes of oxygen non-stoichiometry for the perovskite-type electrode material (La0.8Sr0.2)MnO3 in the temperature range 945–1255 K. A thermogravimetric method was used to monitor the rate of the gas/solid equilibration. For equilibration degrees larger than 0.5, the equilibration kinetic data can be described by a diffusion equation. The determined chemical diffusion coefficient depends essentially on the oxygen partial pressure. Its temperature dependence can be expressed by the following expressions at low and high p(O2), respectively: $$D_{chem} = (1.9 \pm 1.6)10^{ - 3} {\text{exp}}\frac{{{\text{ - }}\left( {{\text{83}}{\text{.4}} \pm {\text{15}}{\text{.8}}} \right){\text{kJ mol}}^{{\text{ - 1}}} }}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (1)}}$$ $$D_{chem} = (1.6 \pm 0.6)10^{ - 1} {\text{exp}}\frac{{{\text{ - }}\left( {{\text{121}}{\text{.2}} \pm 8.2} \right){\text{kJ mol}}^{{\text{ - 1}}} }}{{RT}}({\text{cm}}^{\text{2}} {\text{s}}^{{\text{ - 1}}} ){\text{ (2)}}$$
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Electron Spectroscopy and Related Phenomena 15 (1979), S. 33-37 
    ISSN: 0368-2048
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 77-82 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The preparation of carbonate-containing rare-earth compounds and their thermal decomposition in 0%–17% CO2/N2 gas streams has been studied. Three types of rare-earth carbonate or hydroxycarbonate were produced by precipitation; with ammonium bicarbonate as the precipitant, La2 (CO3)3,CeOCO3 and Ln (OH) x (CO3) y (Sm, Tb, and Yb) were obtained, whereas with Na2CO3, only the normal carbonate, Ln2(CO3)3 (La, Sm, Tb, Er and Yb) was found. Temperature programmed decomposition studies revealed that the normal carbonate decomposed stepwise via a dioxocarbonate, Ln2O2CO3, to the oxide. In contrast, the hydroxycarbonates decomposed directly to the oxide. The presence of CO2 during heating had minimal effect on the decomposition of Ln2(CO3)3 to La2O2CO3 but raised significantly the decomposition temperature of Ln2O2CO3 to the oxide. As CO2 is a major product of the rare-earth oxide catalysed oxidative coupling of methane, these observations indicate that the state of catalyst carbonation will be dependent on the reaction temperature, overall catalyst selectivity and preparative method.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 77-82 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The preparation of carbonate-containing rare-earth compounds and their thermal decomposition in 0%–17% CO2/N2 gas streams has been studied. Three types of rare-earth carbonate or hydroxycarbonate were produced by precipitation; with ammonium bicarbonate as the precipitant, La2 (CO3)3,CeOCO3 and Ln (OH) x (CO3) y (Sm, Tb, and Yb) were obtained, whereas with Na2CO3, only the normal carbonate, Ln2(CO3)3 (La, Sm, Tb, Er and Yb) was found. Temperature programmed decomposition studies revealed that the normal carbonate decomposed stepwise via a dioxocarbonate, Ln2O2CO3, to the oxide. In contrast, the hydroxycarbonates decomposed directly to the oxide. The presence of CO2 during heating had minimal effect on the decomposition of Ln2(CO3)3 to La2O2CO3 but raised significantly the decomposition temperature of Ln2O2CO3 to the oxide. As CO2 is a major product of the rare-earth oxide catalysed oxidative coupling of methane, these observations indicate that the state of catalyst carbonation will be dependent on the reaction temperature, overall catalyst selectivity and preparative method.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 49 (1993), S. 261-269 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Reaction between methane and sulfur vapor (mainly S2) has been studied at 773–1073 K in the presence of possible catalysts and in the absence of a catalyst. Reaction was carried out in a silica tube reactor at a total pressure of 1 atm with excess methane, with prereaction sulfidation using H2S/H2. Sm2O3 had significant catalytic effect on CH4 conversion, but all other potential catalysts (including Li/MgO) gave CH4 conversion close to that in the absence of catalyst. CS2 was the major product, accompanied by C2 coupling product which in most cases was predominantly C2H4 with some C2H6. In some cases, small amounts of C3, C4 hydrocarbons and CH3SH, (CH3)2S, (CH3)2S2 were also found. Experiments with varying space velocity indicated that C2H6 was the primary coupling product. Possible reaction pathways are discussed in terms of homogeneous CH3·generation, augmented by CH3. generated heterogeneously at the surface of sulfided Sm2O3. Sulfidation of Li/MgO is considered to be the reason for the inactivity of this potential catalyst.
    Type of Medium: Electronic Resource
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