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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 2079-2082 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 65 (1994), S. 2156-2158 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A novel synthetic route to the formation of less air sensitive fullerene superconductors by mixing oxygen-containing alkaline compounds with C60 has been discovered. A high-resolution single-crystal x-ray study on the K-doped samples shows that the ratio of potassium to C60 is not 3:1. The observed stability enhancement and the off-stoichiometry of potassium content may originate from the presence of oxygen which serves as an oxidative agent. © 1994 American Institute of Physics.
    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 84 (1986), S. 6401-6409 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The limiting concentration dependence of the heat of transport of electrolyte solutions has been investigated. The ionic contribution to the Onsager phenomenological coefficients for heat-matter coupling Lqi have been calculated by the time-correlation function method using the Fokker–Planck operator as the time-evolution operator. It is shown that the limiting slope due to the direct ion–ion electrostatic effect obtained in the present work agrees with the result in the literature. It is also shown that the contribution to the limiting slope due to ion–solvent interaction may be written in terms of the differences in the Stokes law radii of the ions as well as the reduced ionic heats of transport at infinite dilution. Although our result resembles Agar's result based on a hydrodynamic theory, we point out that there exist substantial differences in the implications of the two results. Finally, an error in the theory of Kahana and Lin [J. Chem. Phys. 75, 5043 (1981)] has been uncovered and corrected.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Section 47 (1991), S. 1575-1581 
    ISSN: 0584-8539
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 179 (1991), S. 237-242 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 18 (1978), S. 19-38 
    ISSN: 1572-9613
    Keywords: Chemical reactions ; fluctuations ; instabilities ; master equation ; renormalization group ; singular perturbations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Two new approaches for investigating critical fluctuations near an instability point of unstable chemical models are proposed. The master equation approach is used. For a homogeneous system without the effect of diffusion, three single-component chemical systems exhibiting critical behavior are considered. The cumulant functions are expanded in a small parameter-the inverse size of the system-and singular perturbation solutions of the master equation are developed. Exponents describing the divergence of the second-order variance are found to be classical. For a system including diffusion effects, spatial correlations for a quasi-one-dimensional case are investigated by considering scale transformation behavior within the multivariate master equation formalism.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1213-1221 
    ISSN: 0887-6266
    Keywords: carbon dioxide ; spin relaxation ; polyisobutylene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Recently we presented the dynamics of 13CO2 molecules sorbed in silicone rubber (PDMS) ascertained from spin relaxation experiments. Results of a similar investigation for 13CO2 sorbed in polyisobutene (PIB) are presented in this report. The spin-lattice and spin-spin relaxation times as well as nuclear Overhauser enhancements (NOE) were determined as a function of temperature and Larmor frequency. The relaxation mechanisms found to be important for 13CO2/PIB system are intermolecular dipole-dipole relaxation and chemical shift anisotropy with a minor contribution from spin rotation relaxation. We have determined the parameters which characterize correlation times for 13CO2 collisional motion, rotational motion, and translational motions in the PIB. The self-diffusion coefficient of 5.15 × 10-8 cm2/s obtained from the nuclear magnetic resonance (NMR) data is close to the literature value of the mutual diffusion coefficient of CO2 in PIB at 300 K obtained from permeability measurements. In contrast to the case of CO2/PDMS in which a broad distribution (characterized by a fractional exponential correlation function of the Williams-Watts type with α = 0.58) is observed, a sharp distribution with a fractional exponent, α, of 0.99 is found for the CO2/PIB system. Instead of assuming an Arrhenius type temperature dependence, we used a Williams-Landel-Ferry type temperature dependence and found it to be better suited to describe the behavior of this system. PIB is a densely packed “strong” chain polymer which responds gradually to the temperature variation and gas sorption. In contrast PDMS is a relatively loosely packed “fragile” polymer with a propensity to exhibit rapid dynamic responses to the temperature change and gas sorption. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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