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〉 88 (1984), S. 2758-2764 
    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〉 90 (1986), S. 3466-3466 
    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
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 6451-6459 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present the results of quasiclassical trajectory (QCT) and quantum centrifugal sudden hyperspherical (CSH) scattering calculations for the Cl+HCl→ClH+Cl reaction using a semiempirical potential energy surface. In particular, we report state-to-state integral and differential cross sections in the vicinity of a transition state resonance that occurs at a total energy E of 0.642 eV. This resonance, which is labeled by the transition state quantum numbers (0,0,2), strongly perturbs the cross sections for the initial rovibrational state HCl(v=1, j=5), which was therefore considered in all our calculations. For E≥0.680 eV, which is well removed from the resonance energy, the QCT and CSH results are in good agreement, but for E near the resonance energy, important quantum effects are found in the integral cross sections, product state distributions, and differential cross sections. The CSH integral cross sections show smooth steplike increases for E≈0.642 eV, which are not seen in the QCT results. Associated with these steps are increased branching to the v'=0 product HCl vibrational state, and a strong propensity for the production of rotational states with j'=15 and 16 for v'=0. These features of the product energy partitioning are not present in the QCT results, although the correct rotational distributions are approximately recovered if the final vibrational action is constrained to match its quantum value. The CSH differential cross sections show a sudden shift from backward to sideward scattering between 0.642 and 0.660 eV, while the QCT cross sections remain backward peaked. An analysis of the "number of atom–diatom encounters,'' during the course of a reactive collision, shows that there are chattering trajectories. These are associated with sideward scattering, but their probability is low and as a result they do not produce distinct features in the angular distributions. However, if the classical deflection function is weighted by the quantum reaction probability, angular distributions are obtained that are in reasonable agreement with the CSH angular distributions (including resonance features).
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5544-5551 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A quantum calculation has been performed using the centrifugal-sudden distorted-wave (CSDW) method for the three-dimensional Cl+DCl→ClD+Cl reaction. Three potential energy surfaces have been employed: two extended London–Eyring–Polanyi–Sato surfaces [denoted Bondi–Connor–Manz–Römelt (BCMR) and Persky–Kornweitz 3 (PK3)] and a scaled and fitted ab initio one (denoted sf-POLCI). Quantities calculated include: cumulative reaction probabilities, integral cross sections, rotational product distributions, and rate coefficients. Differential cross reactions are also reported for the PK3 surface, which are compared with the results from a simple semiclassical optical model (close agreement is found). We also compare the Cl+DCl results with earlier CSDW calculations for Cl+HCl→ClH+Cl. The rotational distributions are strongly perturbed by isotope substitution and are sensitive to variations in the potential surface. In contrast, the H and D rate coefficients for all three surfaces agree with experimental values, except for Cl+DCl on PK3.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 4893-4898 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Quantum calculations of product rotational distributions, cross sections and rate coefficients have been performed for the Cl+HCl→ClH+Cl reaction using the centrifugal-sudden distorted-wave (CSDW) technique. The CSDW method has been shown to be nearly exact at low total energies where the total reaction probability for each partial wave is small. The potential energy surface used is the extended London–Eyring–Polanyi–Sato surface No. 3 of Persky and Kornweitz. This surface has a tighter bending potential near the saddle point than many of the other commonly used Cl+HCl potentials. This difference in bending potential is found to have a profound influence on the product rotational distributions, producing much colder HCl molecules than is the case for the other potentials. In contrast, quantities such as rate coefficients and cumulative reaction probabilities are found to be only weakly sensitive to the strength of the bending potential. Comparison with quasiclassical trajectory results shows reasonable agreement with respect to the shape of the rotational distributions, but the magnitudes of the cross sections and rate coefficients are substantially different.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Reduced dimensionality (RD) cumulative reaction probabilities (CRPs) are reported for the Cl+HCl→ClH+Cl reaction using two semiempirical extended London–Eyring–Polanyi–Sato potential energy surfaces. Comparison is made with CRPs from centrifugal-sudden distorted wave (CSDW) calculations, and with accurate coupled channel hyperspherical (CCH) CRPs for total angular momentum quantum number J=0. Rotational and bending energy-shift approximations are applied to the CCH CRPs for J=0 to obtain approximate CRPs for J〉0. A test of this approximation is made using CSDW partial wave CRPs. New expressions for the thermal rate coefficient are derived using these approximations. The rate coefficients calculated from RD and energy-shifted CCH CRPs are in excellent agreement with each other. They also agree well with the CSDW and experimental rate coefficients.
    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 91 (1989), S. 1668-1687 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new complex angular momentum (CAM) theory of rotationally inelastic scattering has been developed for atom homonuclear–diatomic molecule collisions. The CAM theory is valid for sudden collisions, when the infinite-order-sudden (IOS) approximation for atom rigid-rotator scattering is appropriate. In the IOS/CAM theory, the inelastic scattering amplitude is written in terms of two subamplitudes: a background integral and a residue series. Physically the background integral corresponds to particles scattered by the repulsive potential core, while the residue series corresponds to short lived surface waves that propagate around the potential core. Diffraction effects arise from the interference of these two subamplitudes. The IOS/CAM theory is more general and accurate than the simple Drozdov–Blair theory of inelastic diffraction scattering. The weak coupling limit of the IOS/CAM equations has also been investigated and a new phase rule has been derived that is more general than the Blair phase rule. Approximate conditions for the validity of the new phase rule have been investigated using a model anisotropic potential of the form [g(γ)/r]n, n≥3. Numerical calculations of inelastic angular distributions using the IOS/CAM equations have been made for the strongly anisotropic He–N2 and weakly anisotropic Ne–D2 collision systems. Using a semiclassical approximation to the background integral and a single Regge pole term in the residue series, we obtain good agreement with conventional partial wave IOS angular distributions.
    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 94 (1991), S. 4311-4319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An accurate quantum scattering calculation for the Cl+HCl→ClH+Cl reaction has been performed. In particular, we study the influence of the lowest transition state resonance on the energy dependence of the state-to-state integral cross sections and product rovibrational distributions. The calculations use a recently developed centrifugal sudden hyperspherical (CSH) coordinate reactive scattering code. The Bondi–Connor–Manz–Römelt semiempirical potential energy surface is employed. All 161 partial waves needed for the convergence of the cross sections are included in the calculations. We find that the resonance perturbs certain reagent and product rotational levels of the vibrational ground state (v=0, j=14–16), as well as all open rotational levels (j=0–8) of the first vibrationally excited state (v=1). Transitions from the ground reagent to the ground product vibrational state, such as v=0, j=15→v'=0, j '=15, show almost no resonance structure in the integral cross sections; rather direct scattering dominates the partial wave sum. On the other hand, transitions between perturbed v=0 rotational states and any v'=1 rotational state, or between any v=1 state and perturbed v'=0 states, or between any v=1 and any v'=1 state, show a novel resonance feature in the integral cross sections. This novel feature is a sudden smooth "step'' in the integral cross section, centered at the resonance energy for the partial wave with zero total angular momentum quantum number (J=0). The step has a width equal to the J=0 resonance width. Sometimes this step is superimposed on a slowly varying background which arises from direct scattering. A quantitative description of these resonant steps in the integral cross sections is developed using a J-shift approximation. Because the resonance influences all rotational states for v=v'=1 in a similar way, there is no significant effect on the product rotational distributions due to the resonance. However, the resonance does produce detectable stepping behavior in the product vibrational distribution.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Physics of Plasmas 8 (2001), S. 2835-2848 
    ISSN: 1089-7674
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The polarization current plays an important role in the evolution of magnetic islands with a width comparable to the characteristic ion orbit width. Understanding the evolution of such small magnetic islands is important for two reasons: (1) to investigate the threshold mechanisms for growth of large-scale islands (e.g., neoclassical tearing modes), and (2) to describe the drive mechanisms for small-scale magnetic turbulence and consequent transport. This article presents a two-fluid, cold ion, collisional analysis of the role of the polarization current in magnetic island evolution in slab geometry. It focuses on the role played by the conjunction of parallel electron dynamics and perpendicular transport (particle diffusion and viscosity) in determining the island rotation frequency and the distribution of the polarization current within the island. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Physics of Plasmas 4 (1997), S. 3211-3216 
    ISSN: 1089-7674
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The bootstrap current in a non-Maxwellian tokamak plasma with electron cyclotron heating is calculated. The calculation is exact in the limit of highly charged ions, where pitch-angle scattering dominates over quasilinear diffusion, and shows that the current is entirely determined by the pressure of the trapped electrons. If the ion charge is finite, the current is shown to consist of two terms: one driven by collisions, and one driven by the heating and losses. The former is calculated approximately by using a model collision operator, and is found to be determined by the distribution of trapped electrons alone; the latter is discussed qualitatively.
    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...