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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 8595-8604 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A two-variable Langmuir–Hinshelwood mechanism for isothermal CO oxidation on a catalytically active surface is presented. It shows bistability stemming from 2 cusp bifurcations, which can be obtained analytically for low pressure. Inclusion of CO diffusion on the surface leads to a system of partial differential equations, which exhibits nucleation and front propagation phenomena in the bistable region. While the line of equistability could with good accuracy be solved for analytically, the front velocities and critical radii for nucleation had to be determined numerically (using the method of heteroclinic orbits). Throughout the calculations the kinetics and rate constants for the CO oxidation on Pt(111) are used. Here the model can be reduced by adiabatic elimination of one variable (namely oxygen coverage) allowing a comparison to the exactly solved one-variable Schlögl model. Possible implications for future experimental work are briefly discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 5193-5204 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A Pt single crystal of cylindrical shape (axis II [001]) whose surface exhibits all orientations of the [001] zone has been used to study coupling effects between orientations which exhibit kinetic oscillations in catalytic CO oxidation. On the clean surface, one can distinguish between an orientational range in between (110) and (320) which exhibits a 1×2 reconstruction, a nonreconstructed surface range around (210) and a hex reconstructed surface range around (100). Structural transitions proceed continuously via atomic steps between (110) and (210), while the orientational range extending from (210) to (100) is faceted. With a rotatable Kelvin probe, the orientational dependence of the work function could be followed. The results revealed that the variation of the oxygen sticking coefficient sO2 displays a mirror-like behavior with respect to the work function variation of the clean surface such that the orientation with the lowest work function (210) exhibits the highest sO2. Kinetic oscillations were studied in the 10−5 and 10−4 Torr range. By means of two Kelvin probes, the Δφ oscillations could be followed simultaneously at two different orientations, while the integral behavior of the cylinder surface was monitored via the CO2 production rate. A strong broadening of the oscillatory region in parameter space, as compared to a flat surface, was detected for the oscillatory range around (100). In the vicinity of this orientation, spatial coupling is provided via reaction fronts which propagate from (210) toward (110). Gas-phase coupling is only observed with the (110) orientations. Prolonged oscillation experiments cause faceting resulting in an increase of catalytic activity around (100), while the orientations around (210) lose catalytic activity by faceting.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 307-319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The periodically perturbed oscillations in the isothermal CO oxidation on a Pt(110) surface at low pressure were modeled using the recently developed reconstruction model of kinetic oscillations, in which the usual Langmuir–Hinshelwood mechanism is coupled with the CO-driven 1×2(arrow-right-and-left)1×1 phase transition of the surface. The experimental findings (entrainment bands, quasiperiodicity, critical slowing down) could be well reproduced with this model. The calculations revealed a complicated bifurcation fine structure of the Arnol'd tongues. While the skeleton structure turned out to be the same as in other studies, some additional features were found, and several details (mainly in the p/2 tongues) were different from forced systems examined previously. A co-dimension-3 bifurcation (in which a second-order resonance coincides with a degenerate period doubling) is discussed in this context.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 1582-1589 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The NO+CO reaction, which has been shown to exhibit damped kinetic oscillations on a Pt(100) surface after initial excitation, has been subjected to periodic and random forcing of the temperature and of the CO partial pressure. The experiments were conducted in the 10−7 mbar range and measurements of the CO2 production rate and of the work function were used to follow the response of the system. The response behavior is characterized by strong resonance effects and by the absence of quasiperiodic oscillations. The system is highly sensitive to temperature modulation, but rather insensitive to modulation of pCO with the latter requiring an amplitude of more than 5% of pCO for producing sustained oscillations. Random forcing experiments demonstrate that the response of the system can be described as a bandpass filter since only frequencies close to the natural frequency of the system are amplified. The results of the experiments led to the conclusion that the damping effect is due to the absence of an efficient synchronization mode under isothermal conditions at low pressures.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 9161-9172 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The parameters entering the kinetics for the mechanism of catalytic CO oxidation have been adapted for a Pt(110) surface, giving rise to a two-variable model correctly predicting bistability. Oscillations are obtained when, in addition, the adsorbate-driven 1×2–1×1 structural phase transition of Pt(110) is taken into account. Mixed-mode oscillations can be qualitatively explained by including the faceting of the surface as a fourth variable. The limitations of the model essentially stem from the fact that only ordinary differential equations have been analyzed so far neglecting spatial pattern formation. It is discussed which dynamic phenomena observed experimentally in the CO oxidation on Pt(110) will probably not be adequately describable without taking spatial effects into account.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 12 (1992), S. 331-344 
    ISSN: 1572-879X
    Keywords: XPS of Pt black catalyst ; UPS of Pt black catalyst ; surface state of Pt black ; catalytic properties of Pt black
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract XPS and UPS of a Pt black catalyst after customary H2-O2 regeneration shows considerable amounts of residual C as well as surface OH/H2O species. Surface C could not be removed even by O2 at 800 K. Oxygenates are stable even after H2 treatment up to 750 K. Their chemical state has been tentatively identified by comparing XPS and UPS results. Catalytic transformations of n-hexane on Pt black treated analogously is reported and the effect of surface species on catalytic properties discussed. Possible consequences of the presence of stable surface OH/H2O species on H2-O2 titrations are mentioned.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-879X
    Keywords: Ammonia synthesis ; Ru-zeolite ; metal clusters ; conversion measurements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Na-Y zeolite was cation exchanged with Ru(NH3)6Cl3 yielding at 25% exchange level a light-purple solid which was active in ammonia synthesis at atmospheric pressure. Pulse conversion experiments show that the catalyst stores nitrogen as it was observed with the conventional iron catalyst. At 810 K the conversion reached about 20% of the maximum conversion of the iron catalyst. The catalyst deactivated reversibly within 30 h due to agglomeration. The active species in the catalyst is most likely a cluster-like Ru metal particle prevented from sintering under the reducing conditions of catalysis by the zeolite framework.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Na—Y zeolite was cation exchanged with Ru and tested in ammonia synthesis at atmospheric pressure. Activities up to ∼10% of the commercial iron catalyst scaled by the active surface area were observed. Characterization of the zeolites with XPS was complemented with reference thermal desorption spectroscopy data on a polycrystalline Ru metal surface. The catalysts showed high thermal stability in in situ reduction-oxidation cycles. The chemical state of the Ru will be discussed. From shift measurements the Ru is metallic in the active state, but line shape arguments point to a cluster-like particle morphology. The location of the Ru inside or outside the zeolite framework will be discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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