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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 3 (1987), S. 1098-1102 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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 93 (1990), S. 8306-8313 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Kinetic oscillations in catalytic reactions are often attributed either to attractive absorbate–absorbate interactions between adatoms or to required vacant sites for chemical reaction and are usually described by ordinary differential equations. These mechanisms are examined as possible causes for oscillations in surface reactions using Monte Carlo simulations. Self-sustained oscillations driven by a phase transition on the catalyst surface are found. It is shown that spatial inhomogeneity of the surface controls the existence of oscillations which therefore cannot be modeled using ordinary differential equations. The problem of synchronization of numerous oscillators on the surface is investigated. In particular, the influence of adatom migration and surface defects on Hopf bifurcation is examined. It is demonstrated that sites on surface with strong binding energy result in more chaotic oscillations whose amplitude decreases. The influence of concentration and distribution of defects on the kinetic oscillations is discussed.
    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 91 (1989), S. 5374-5386 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Oscillations with large amplitudes (〉500 K), high frequencies (〉8 Hz), and good reproducibility are observed in methylamine decomposition on electrically heated Pt, Rh, and Ir wires at pressures of 0.25–8.0 Torr and temperatures between 900 and 1500 K. The major reaction involves formation of HCN which is endothermic by 37 kcal/mol, so that the reaction strongly cools the wire, which counteracts resistive heating. A photodiode array was used to monitor spatial and temporal oscillations with resolutions of 1 mm and 30 Hz, respectively. On Pt, the frequency increased with increasing pressure and with decreasing wire diameter, while amplitude was a weak function of these parameters. On Ir, oscillations were more complex with regions of the wire often oscillating independently and more variability between experiments. However, the overall behavior resembles that on Pt. On Rh, frequencies were much lower (〈0.03 Hz), oscillations occurred over a smaller temperature range and halves of the wire frequently oscillated out of phase with each other. Oscillatory behavior of methylamine decomposition on Pt was modeled by a simple lumped model which gives semiquantitative agreement with observations. The model assumes a simple unimolecular reaction with CH3NH2 adsorption blocked at low temperatures by formation of a strongly adsorbed CN which is known to be very stable on Pt (Ed (approximately-equal-to)50 kcal/mol). Calculated frequencies, pressure dependencies, amplitudes, and temperature range of oscillations agree quite well with experiments using reasonable values for adsorption and reaction rate parameters, and wire geometry and properties.
    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 88 (1988), S. 6597-6604 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Surface diffusion of hydrogen, deuterium, and CO on Rh(111) has been investigated by laser-induced thermal desorption (LITD) and compared with previous results for these species on Pt(111) and on other metals. As the coverage θ of deuterium increases from 0.02 to 0.33, the preexponential factor D0 remains constant at 8×10−2 cm2/s, but the diffusion activation energy Ediff rises from 3.7 to 4.3 kcal/mol. Ediff for hydrogen is 0.6 kcal/mol lower than for deuterium, consistent with the difference in zero-point energy. For CO, Ediff =7 kcal/mol at all coverages, but D0 rises from 10−3 to 10−2 cm2/s between θ=0.01 and 0.40. Values of Ediff for these adsorbates vary by several orders of magnitude for surfaces on which heats of adsorption are essentially identical. These differences appear to correlate with differences in heats of adsorption in different binding states which form saddle point configurations in surface diffusion. Ediff is found to be nearly identical to the reaction activation energies for the CO and hydrogen oxidation reactions on Rh and on several other transition metal surfaces. This suggests that surface diffusion of the reducing agent may be the rate-limiting step in their bimolecular surface reactions.
    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 92 (1990), S. 745-756 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Complex behavior of an oscillating reaction on an array of catalytic regions was modeled using a distributed model consisting of a 10×10 matrix with ten randomly placed oscillators coupled via heat transfer. Each single oscillator was described by a very simple system of two differential equations chosen to model the CO/NO reaction on supported Pd. However, the coupled system exhibited very complex behavior with periodic oscillations, period multiplications, beat structures and chaos. All of these complex features predicted by the model have also been found in experiments. In addition, the model was able to predict the experimentally observed tendencies in the development of complex behavior with changing reaction conditions. Changing distributions of the cells or introducing small differences in the description of the single oscillators did not change the principal features of the system. However, the transition to chaos could be changed in that for one distribution of active cells a Feigenbaum sequence to chaos was found but not in another. With one oscillator twice as active as the rest of the cells, the high activity cell was dominant and entrained the whole system, leading to completely synchronized behavior. Also in this situation, however, chaotic responses were found, when the high activity oscillator was in a stable ignited state. Possible generalizations of this treatment to other oscillating systems are discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 4679-4686 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electron energy loss spectroscopy (EELS) has been used to study the adsorption of nitric oxide on Rh(111). NO adsorbs in twofold bridge sites at all coverages. The dissociation rate of NO on this surface at low coverage has been measured directly using EELS. The first order dissociation rate parameters are Ea =19.2±0.3 kcal/mol and ν(1)0 =1×1014±0.3 s−1 at θNO ≈0.2. Ordered low energy electron diffraction (LEED) patterns are observed only for partially dissociated NO adlayers and not for NO adsorbed molecularly at 95 K. Because NO adsorbs in twofold bridge sites at all coverages, the N–O stretching frequency exhibits a 150 cm−1 shift from zero to saturation coverage.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 4687-4695 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High resolution electron energy loss spectroscopy has been used to examine the effects of coadsorbed oxygen and carbon monoxide on the bonding of nitric oxide adsorbed on the Rh (111) surface. NO is converted from twofold bridge sites (1500–1600 cm−1) to linear sites (1840 cm−1) when annealed to 275 K in the presence of coadsorbed oxygen. Terminally bound linear NO does not dissociate, but desorbs molecularly, a finding consistent with the commonly observed oxygen inhibition of NO dissociation over noble metals. Coadsorbed CO does not significantly inhibit or promote the dissociation of a low coverage of nitric oxide compared to the clean Rh (111) surface. CO and NO appear to segregate and form islands of each species at 95 K if CO is adsorbed first. Annealing this adlayer above 250 K disperses the islands and mixes the adsorbate layer at temperatures below where NO dissociation and reaction with CO are significant. The Rh–CO bond is weakened in well-mixed CO+NO adlayers, indicating that the NO–CO repulsive interaction acts through the Rh substrate rather than directly between the adsorbed molecules.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 40 (1948), S. 607-620 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 4908-4914 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 6194-6200 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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