Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 76 (1972), S. 442-446 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 958-963 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 8327-8333 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 8334-8343 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 6880-6890 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The binding energy, surface energy, surface atom coordination numbers, and bond lengths and angles of small clusters at low temperatures are calculated with parameters fitted to Ni using both the Lennard-Jones (LJ) potential and the embedded atom (EA) potential to assess the sensitivity of interatomic potential on cluster structure. Simulations are performed by implementation of the simulated annealing method in a canonical ensemble Monte Carlo technique. We examine clusters with n≤34 atoms and we find that they are noncrystalline (with the exception of n=6). The most stable structure of clusters consisting of n≤15 atoms and n=19 atoms is the same for both potentials (with the exception of n=8). However, the most stable structure of clusters with n≥16 atoms is different for the two potentials (with the exception of n=19). Smeared angular distribution and pair distribution functions are found for many EA clusters whereas sharp, well defined peaks exist for LJ clusters. A discontinuous transition from polyicosahedral to quasicrystalline structure is found from n=30 to n=31 atoms for the LJ potential. This transition occurs at smaller n for the EA potential. Surface atom coordination numbers are found to be nonmonotonic functions of cluster size. The existence of multiple structures of small clusters and the effect of quenching rate during crystallization on the final shape of clusters are also examined.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...