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
    Biochemistry 21 (1982), S. 3831-3835 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    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.] : Macmillan Magazines Ltd.
    Nature 387 (1997), S. 580-583 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Biosensors are molecular sensors that combine a biological recognition mechanism with a physical transduction technique. They provide a new class of inexpensive, portable instrument that permit sophisticated analytical measurements to be undertaken rapidly at decentralized locations. However, ...
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 51-58 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Amorphous polymers are assumed to possess a quasicrystalline structure with chain bundles that are locally parallel over distances ∼1 nm. Two possible types of random motion for a spherical penetrant in such a substrate are described, one type determining the jump frequency and activation energy of diffusion, the other type determining the jump length. The former quantities may be calculated from the model, but not the latter. Sorption of simple gases at low penetrant pressures is assumed to occur mostly in pre-existing holes, both above and below Tg, and the same penetrant diffusion mechanism is assumed to hold in the two regions. The changes in apparent heat of solution and activation energy of diffusion observed at Tg are explained in terms of additional hole formation with increase in temperature above Tg. The theory is shown to be consistent with experimental diffusion data for several glassy and rubbery systems. Evidence is given that hole formation in simple polymers such as polyethylene may occur by chain “kinking”. For polymers possessing articulated side groups, however, it appears that hole formation arises principally from motions within these groups.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Following Di Benedetto it is proposed that noncrystalline polymer regions possess an approximate semicrystalline order with chain bundles that are locally parallel along distances of several nanometers. Packing with on-average four nearest neighbors is assumed. A spherical molecule may move through such a substrate in two distinct ways: (a) along the axis of a “tube” formed by locally parallel chains or (b) perpendicular to this axis by two polymer chains separating sufficiently to permit passage of the molecule. The first process is relatively fast, generally requires little activation energy, and determines the effective jump length in diffusion. The second is responsible for the activation energy of diffusion, which is taken as the minimum energy necessary to produce a symmetrical chain separation which allows transfer of a molecule. This is calculated as a function of the penetrant diameter d and parameters Γ and β which characterize the interchain cohesion and chain stiffness, respectively. Γ is estimated from the polymer density and cohesive energy density by suitably linearizing a relation given by Di Benedetto for the potential between two polymer chains approximated as infinite strings of Lennard-Jones force centers. β is shown to be approximately obtainable from the polymer chain backbone geometry and bond rotation potentials. An expression for the diffusion coefficient D is developed which contains only one disposable parameter, the effective jump length.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory developed in Part I of this series is modified to accommodate polymers that possess closely spaced, bulky side groups on the chains. The side groups give rise to free space between the chain “cores,” which reduces the chain separation required for penetrant motion transverse to the local chain axis. The theory is then identical to that of Part I, except that penetrant diameters minus a constant factor are employed in place of the normal diameters. In most of the cases studied the reduction factor for a given polymer may be estimated with reasonable precision from chain geometry data. This diameter-reduction effect is the likely explanation of the apparent proportionality between the activation energy of diffusion and the square of the penetrant diameter reported earlier for vinyl polymers. The data quoted here and in Part II are analyzed to give a semitheoretical correlation between the effective jump length L̄ and ΔE, the activation energy of diffusion. This correlation appears to be equally valid for glassy and rubbery noncrystalline polymers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory developed in Part I of this series is applied to a number of nonvinyl “smooth” chained homopolymers. The agreement between predicted and observed activation energies of diffusion for simple penetrants is generally good, particularly for polyethylene. Discrepancies observed for the smallest penetrants, He and H2, in some polymers may be rationalized in terms of atomic scale irregularities on the polymer chain surface. It is shown that in favorable cases the theory may permit diffusion data to be used as an additional check on the accuracy of conformational energy maps for polymers.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1675-1692 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A previously developed model of simple penetrant diffusion is extended to encompass complex penetrants of idealized molecular shape, characterized by dimensions of length, width, and thickness. Expressions are obtained for D(0,T), the diffusion coefficient at zero penetrant concentration (c), and the fractional increase in D(0,T) as a function of c and temperature (T). The model predicts that D(0,T) will exhibit Arrhenius behavior at temperatures well above Tg and gives the limiting activation energy as a function of penetrant thickness and the polymer energy/distance constants used previously. For Tg 〈 T ≲ Tg + 150 K the model requires two new disposable parameters, in addition to the jump-length parameter of the simple penetrant theory. These parameters, however, have precise physical meanings (all are lengths) and together with the penetrant dimensions and polymer constants determine the absolute magnitude of the diffusion coefficient as well as its relative dependence on c and T. For T ≳ Tg + 40 the relative concentration dependence may be calculated in terms of the penetrant dimensions and polymer constants only.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1693-1708 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The theory of Part I is applied to the diffusion of several aromatic diffusants in two “smooth chained” polymers: poly(ethylene terephthalate) (PET) and natural rubber. Modifications of the theory necessary to accommodate vinyl polymers are discussed and applied to benzene in PMA and PEA. In all cases the theory agrees satisfactorily with the experimental D(0,T) and D(c,T)/D(0,T) data, and the values of the disposable rg and Δ parameters are of the expected order. The limiting Arrhenius behavior of benzene in natural rubber appears to be correctly predicted. The cell model is definitely more appropriate than the free volume model for the calculation of enfolding chain effects in highly crystalline PET. For the three amorphous polymers the two models give comparable results, the cell model being somewhat superior for natural rubber and PMA.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 1657-1658 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1103-1124 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model of simple molecule sorption in polymers is proposed which embraces both the glassy and rubbery regions, and incorporates the successful dual-mode model below the glass-transition temperature. Hole filling is shown to be an important sorption mechanism both above and below Tg, although saturation effects do not occur in the rubbery polymer. The model interprets the “dual-mode” Langmuir and Henry's law parameters at the molecular level, and a simple statistical mechanical analysis allows estimation of the parameter values, as well as specifying certain interrelationships between the parameters. Applications of the model to gas solubility data in five polymers are considered [polyethylene (PE), poly(ethylene terephthalate) (PET), polystyrene (PS), polymethacrylate (PMA), poly(vinyl acetate) (PVAc)] and semiquantitative agreement is obtained for PE, PET, and to a lesser extent, PS. For PMA and PVAc, the agreement is qualitative only.
    Additional Material: 14 Ill.
    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...