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  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 4830-4834 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 492-499 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 75 (1994), S. 2312-2316 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The stopping power for hydrogen (1H)and helium (4He) in thermally imidized pyromellitic dianhydride-oxydianaline polyimide was measured using the thin-film backscattering method. As the incident energy increased from 1 to 3 MeV, the hydrogen stopping power decreased from 4.2 to 1.8 eV/(1015 atoms/cm2), whereas the helium stopping power decreased from 33.6 to 18.6 eV/(1015 atoms/cm2). These results were in excellent agreement with values predicted by either Bragg's rule or the cores-and-bonds model. This work demonstrates the advantages of using spun-cast thin (〈3 μm) polymer films supported on silicon wafers for stopping power measurements. Prior measurements of the stopping power relied on transmitting the ion beam through relatively thick (∼10 μm) free-standing films where the uncertainty in the film thickness often introduced significant systematic errors. With polymer films supported on silicon, ellipsometry can be used to accurately determine film thickness.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 26 (1991), S. 2815-2822 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The concentration versus depth profile in diffusion couples initially consisting of layers of pure polystyrene (PS) and poly(xylenyl ether) (PXE) were measured. To reveal the profile, the PXE molecules (after diffusion) were preferentially stained in the glass by exposing the couple to a solution of 2 mol % Br in methanol; the covalently bound Br nuclei serve as heavy nuclear tags which permit a sensitive determination of the PXE depth profile by Rutherford backscattering spectrometry (RBS). The samples were annealed at temperatures, T, ranging from 177–210 °C that are above the glass transition temperature, T g, of the pure PS (105 °C) but below the T g of pure PXE (216 °C). The measured concentration versus depth profile is markedly asymmetric, with a low slope at low values of the volume fraction of PXE, φPXE, but with a much greater slope at high values of φPXE. These results are in qualitative agreement with the variation in the mutual diffusion coefficient, D, expected as φPXE increases, causing the T g of the blend to increase towards, and finally exceed, the diffusion temperature. Values of D extracted from these concentration versus depth profiles at low values of φPXE using the Boltzmann-Matano analysis are in good agreement with those measured by forward recoil spectrometry (FRES) in deuterated-PS: PXE couples with only small composition differences.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 26 (1991), S. 2815-2822 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The concentration versus depth profile in diffusion couples initially consisting of layers of pure polystyrene (PS) and poly(xylenyl ether) (PXE) were measured. To reveal the profile, the PXE molecules (after diffusion) were preferentially stained in the glass by exposing the couple to a solution of 2 mol % Br in methanol; the covalently bound Br nuclei serve as heavy nuclear tags which permit a sensitive determination of the PXE depth profile by Rutherford backscattering spectrometry (RBS). The samples were annealed at temperatures,T, ranging from 177–210 °C that are above the glass transition temperature,T g, of the pure PS (105 °C) but below theT g of pure PXE (216 °C). The measured concentration versus depth profile is markedly asymmetric, with a low slope at low values of the volume fraction of PXE, φPXE, but with a much greater slope at high values of φPXE. These results are in qualitative agreement with the variation in the mutual diffusion coefficient,D, expected as φPXE increases, causing theT g of the blend to increase towards, and finally exceed, the diffusion temperature. Values ofD extracted from these concentration versus depth profiles at low values of φPXE using the Boltzmann-Matano analysis are in good agreement with those measured by forward recoil spectrometry (FRES) in deuterated-PS: PXE couples with only small composition differences.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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