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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 6832-6838 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 112 (1990), S. 5750-5759 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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. 4593-4596 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have measured the rate coefficients for radiative (RCT) and dissociative (DCT) charge transfer from He+ to H2 at temperatures 15(approximately-less-than)T(approximately-less-than)40 K. We find the radiative charge transfer reaction to be essentially independent of temperature, while the rate coefficient for the dissociative reaction increases with increasing temperature in this temperature range. We compare our results with those of other experimenters and comment on sources of uncertainty unique to this experiment.
    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 92 (1990), S. 3442-3447 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The tandem flowing afterglow-selected ion flow tube was employed to study the isotopically labeled reactions of O−+N2O→NO−+NO at 300 K. In the reactions of 16O−+15N14N16O, 16O−+14N15N16O and 18O−+14N14N16O, both of the possible NO− products are formed with equal probability, indicating that equilibration is achieved within the reaction complex before dissociation. In the totally labeled reactions of 18O−+15N14N16O and 18O−+14N15N16O all possible NO− products are observed which strongly supports the formation of both trigonal and linear N2O−2 intermediates along the reaction path. The reaction mechanism is discussed and these results are compared with those of other workers.
    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 85 (1986), S. 3851-3859 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In the gas phase O+2 reacts with methane at 300 K to produce a hydrogen atom and the CH3O+2 ion. The structure of this ion has recently been determined to be H2COOH+, methylene hydroperoxide ion. The reaction rate coefficients and product distributions have now been measured at 300 K for the CHnD4−n isotopes. The reaction shows both inter- and intramolecular isotope effects, e.g., CH2D2 reacts more slowly than methane and more rapidly than CD4, but loses hydrogen or deuterium with equal probability. The ion readily transfers HO+ to alkenes, CS2, and many other neutral molecules. The reaction with CS2 has been used to investigate the isotopic distribution within mixed isotope product ions. In addition, the reaction rate coefficients for both CH4 and CD4 have been measured as functions of temperature between 20 and 500 K; in both cases a clear minimum is observed in the reaction rate coefficient near room temperature. A mechanism for the reaction is proposed which allows us to model the temperature dependence of the reaction rate coefficient over the entire range for which there are data.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 90 (2001), S. 1612-1624 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The common description of the electrostatic force, F(x)=−q∇φ(x), provides an incomplete description of the force on the charge q at a point x when the charge itself induces additional fields, e.g., image charges, polarizations, etc. The equation may be corrected through the introduction of a "pseudopotential" formalism. Exploration of some of the elementary properties of the pseudopotential demonstrates its essential simplicity. This simplicity allows it to be incorporated directly into dynamics calculations. We explicitly evaluate the pseudopotential in a number of simple but important cases including the sphere, parallel plates, the rectangular prism, and the cylindrical box. The pseudopotential formalism may be expanded to include extended charge distributions; in this latter form we are able to directly apply the results to experimental measurements. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 2772-2777 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 481-488 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Pulsed-laser-irradiated surfaces sometimes emit positive ions at energies several volts higher than one would expect, even at modest (〈0.1 J/cm2) fluences. A mechanism that can account for this phenomenon is discussed. Intense surface photoemission of electrons during the laser pulse leads to the formation of a space-charge layer near the surface. If the laser fluence were constant, the ions would accelerate and subsequently decelerate as they pass through this steady potential well. As the laser pulse ends, however, some ions may undergo extended acceleration as this space-charge layer moves away from the surface. The maximum possible ion acceleration is analytically calculated and the acceleration for a range of realistic experimental parameters is numerically predicted. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Physics of Plasmas 3 (1996), S. 2859-2863 
    ISSN: 1089-7674
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A scheme that allows stable confinement of a weakly ionized non-neutral plasma is discussed. The method requires the forced rotation of the neutral gas within the trap about an axis that roughly coincides with the trap's magnetic and mechanical axes. A number of the basic equilibrium and nonequilibrium properties of such a trapped plasma are calculated. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 4877-4886 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The destruction of low concentrations (〈1000 ppm) of gas-phase carbon tetrachloride (CCl4) using a low-temperature, dielectric barrier/packed-bed corona reactor was studied. We compare, in particular, the destruction efficiencies using either borosilicate or zirconia oxide (ZrO2) packing materials in dry and moist air, and nitrogen buffer gases. Measurements of contaminant removal in the effluent gas were made at atmospheric pressure as a function of energy dissipated in the reactor. In dry N2, destruction of CCl4 was most efficient using ZrO2 beads, whereas, in dry air, contaminant removal was approximately equal for borosilicate glass and ZrO2. The presence of water in the gas stream reduced the CCl4 destruction efficiency under all conditions. This reduction was likely a synergistic effect that involves changes in the plasma density, scavenging of low energy secondary electrons, and possible surface passivation. Assuming the primary step in CCl4 destruction is dissociative electron attachment, an estimate of the average density of low energy electrons as a function of input energy was made. We relate the enhancement in CCl4 destruction using the ZrO2 beads in N2 to a slight increase in the number density of low energy secondary electrons. A discussion of the importance of energy density measurements and a useful phenomenological kinetic model consistent with the observed results are presented. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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