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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 5522-5533 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 11283-11285 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-879X
    Keywords: EXAFS ; Pt/Al2O3 catalyst ; temperature ; pressure ; carbon deposition ; carbon removal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract EXAFS has been used to follow in situ the structural evolution of a Pt/Al2O3 catalyst during removal of carbon by hydrogenation, after reduction and carbon deposition. After reduction at 350 °C, the total hydrogen pressure was raised to 3 atm. and n-heptane was injected over the sample. EXAFS measurements at the Pt edge were carried out with simultaneous on-line EXAFS analysis of the spectra. After observing the rapid formation of a carbon-platinum bond which is unmodified with time, we stopped the heptane flow, raised the temperature to 450 °C, and maintained hydrogen flow at 3 atm. The disappearance of the platinum-carbon bond during heat treatment in hydrogen was monitored via on-line analysis. No sintering of the metal particles was observed. EXAFS is thus proven to be an efficient tool to study not just structural changes of a catalyst during a hydrocarbon reaction [1], but also to use it as a technique to study other catalytic phenomena as well.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-879X
    Keywords: EXAFS ; Pt/Al2O3 catalysts ; chlorine ; temperature ; pressure ; reduction ; deactivation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract EXAFS has been used to follow in situ the structural evolution of a chlorinated and non-chlorinated Pt/Al2O3 catalyst during reduction in the temperature range of 300–500 °C. Smaller metal clusters are formed from the hydrogen reduction of the chlorinated catalyst, in contrast to the larger cluster formed from the non-chlorinated one. At 460 °C, the total hydrogen pressure was raised to 5 atm. and n-heptane was injected over the samples. EXAFS measurements at the Pt edge were carried out while hydrocarbon conversion was monitored with a gas Chromatograph. We observe the rapid formation of a carbon-platinum bond. This is unmodified while turnover rates and selectivities indicate evidence for deactivation. From this structural information supplied by EXAFS, correlated with the data obtained from gas chromatography, we find that our results are consistent with a model proposed by others where deactivation is due to the build-up of a multilayer of carbon.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-879X
    Keywords: EXAFS ; Pt ; Pt-Re ; Pt-Sn ; in situ ; deactivation ; coking ; sintering
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Extended X-ray absorption fine structure (EXAFS) spectroscopy has been used to study the structural evolution of monometallic (Pt/Al2O3) and bimetallic (Pt-Re/Al2O3) catalysts with metal loadings representative of those used industrially under conditions close to those seen during preparation (calcination and reduction), during catalysis (under a hydrogen-hydrocarbon mixture), and during regeneration (simulated by cycles of reduction and oxidation). During the catalytic reforming ofn-heptane, the formation of bonds to carbon species is observed directly by EXAFS. Despite the fact that only platinum-carbon bonds are observed, bimetallic systems show significant differences compared with monometallic systems with, in the case of Pt-Re, a reduction in the temperature range over which carbon bonding is observed, and structural modifications of the metallic particles. Under the same conditions, no carbon bonding is observed for the Pt-Sn system. In the case of Pt-Sn/Al2O3, the EXAFS results, confirmed by transmission electron microscopy, demonstrate the high resistance to sintering of this bimetallic system compared to the monometallic system.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 28 (1993), S. 5019-5031 
    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 Uniform particles of controlled morphology of CeOSO4·H2O may be prepared by forced hydrolysis, at 90 °C, of solutions of cerium (IV) sulphate. A structural description is given here of the different steps of the forced hydrolysis before precipitation takes place. It uses essentially the complementary techniques of extended X-ray absorption fine structure spectroscopy and small-angle X-ray scattering to characterize, at different length scales, the structural evolution of the solution. The first step, which occurs as temperature is raised above 60 °C, is an inorganic polymerization that transforms molecular dimeric precursors Ce2(OH)2O12 into colloidal particles. In the second step, at the ageing temperature of 90 °C, no chemical and structural changes are revealed; the solution has reached an equilibrium state characterized by the presence of 3 nm large monodisperse colloids which use 85% of the initial cerium ions and smaller particles (15%). The detailed local structure around the cerium atoms in the colloids is compatible with the formation of a chain-like structure of Ce(IV) ions via hydroxo bridges (Ce(OH)2) n 2n+ . A mechanism to explain the transformation of precursors into colloids is proposed.
    Type of Medium: Electronic Resource
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