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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 9337-9342 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Creep experiments were carried out on amorphous selenium (Se) at temperatures in the vicinity of the glass temperature. The recoverable compliance lacks a plateau, indicating Se chains are too short to form an entanglement network. The measured compliance function was thermorheological complex, even after subtraction of the glassy level and normalizing by the steady state compliance. The temperature dependence determined from the viscosity was in accord with previous viscosity data, although weaker than the near-Arrhenius dependence deduced from the stress relaxation of Se. Based on a comparison to other, small-molecule glass-formers, the dynamic fragility calculated from the viscosity was larger than expected from Se's thermodynamic fragility (i.e., steepness of the normalized Kauzmann curve). In contrast, although polypropylene (PP) is substantially more dynamically fragile than Se, PP is less thermodynamic fragile. Thus, when compared to either small-molecule liquids or polymers, Se exhibits a disconnect between dynamic and thermodynamic measures of fragility. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 5593-5598 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The energy landscape model of the glass transition has received increasing attention, due to its potential for providing a thermodynamic interpretation of the dynamics of glass-forming liquids. Herein, the idea that the temperature-dependence of the dynamics near the glass temperature ("fragility") can be related to thermodynamic properties is tested for polymers. Previously, for several homologous series, we found deviations from a proposed correlation between fragility and the heat capacity increment at the glass temperature. A survey of 17 polymers likewise indicates no correlation between these two quantities. More recently, the landscape approach to the dynamics of glass-formers was extended to a proposal that fragility can be determined a priori from thermodynamic information. However, for the 11 polymers for which sufficient thermodynamic and relaxation data were available, we find that thermodynamic properties bear no relationship to fragility. Thus, it appears that the status of the glass transition as an important unsolved problem in condensed matter physics remains intact.
    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 110 (1999), S. 11585-11591 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Dielectric relaxation measurements were performed on propylene glycol (PG) and oligomers having different number of repeat units (N=2, 3, and 69). The primary α-relaxation had the Kohlrausch–Williams–Watts (KWW) form, with a stretch exponent (1−n) which decreased with increasing N. The temperature dependence of the α-relaxation time, as reflected in the fragility index, increased with N. A broad, rather symmetric secondary β-relaxation was observed at higher frequencies in the dielectric loss spectrum for all samples with N〉1. This is the first observation of the β-relaxation peak in dipropylene glycol (N=2) and tripropylene glycol (N=3). The separation between the α- and β-relaxations increased with increasing N. This trend indicates that the separation is minimal in PG, which makes it difficult to resolve the β-relaxation from the more intense α-relaxation. This, together with the fact that the strength of the β-relaxation decreases with the molecular weight of PPG, as found by Johari and coworkers, explains the absence of an observable β- peak or shoulder in isothermal or isochronal dielectric measurement on PG. It is proposed that the deviation of the dielectric loss peak for PG from either the KWW or the Cole–Davidson functions at higher frequencies is due to a β-relaxation masked by the α-process. The same conclusion was reached by Johari and co-workers, based on evidence from their "difference isochrone method." Finally, we show that the data from oligomers of propylene glycol support the recently proposed correlation of τβ(Tg) with (1−n) and the rough agreement between τβ(Tg) and the primitive relaxation time of the coupling model at temperatures above Tg.
    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 106 (1997), S. 1187-1190 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Coupling model analyses of short-time relaxation data of glycerol from quasielastic neutron scattering and ortho-terphenyl (OTP) by molecular dynamic simulation are shown to account for both the time dependence of the correlation function and its temperature dependence. The latter is expressible over a limited temperature range as an Arrhenius relation with an apparent activation energy for the fast α-relaxation process, with EA=6.2 and 3.9 kcal/mol for glycerol and OTP, respectively. The viscosities of these glass formers have also been measured up to temperatures sufficiently high that the mean viscosity relaxation time, 〈τη(T)〉, becomes short, approaching the crossover time, tc(approximate)2 ps, of the coupling model. When this condition is realized, 〈τη(T)〉 becomes comparable to τD(T) in both magnitude and temperature dependence. Hence, the asymptotic high temperature activation energy of 〈τη(T)〉 approximately equals the apparent activation energy of τD. The experimental data, supporting this connection between macroscopic variables such as viscosity and microscopic dynamics from neutron scattering and molecular dynamics simulation, indicate the significance of the fast α-relaxation process in both fragile and strong liquids.
    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 104 (1996), S. 2967-2970 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The correlation between the magnitude of the Debye–Waller anomaly and the temperature dependence of the relaxation time and viscosity of glass-forming liquids (i.e., their fragility) is investigated using the coupling model of relaxation. The correlation is shown to be a natural consequence of the relationship between the noncooperative and intermolecularly cooperative relaxation times of the model. Specifically, the deviation of the mean squared displacement from a linear temperature dependency increases as the fragility (in the Angell sense) of the glass-forming liquid increases because more fragile glasses exhibit substantially more short-time, noncooperative relaxation. This latter fact arises from their shorter noncooperative relaxation times, as deduced from the coupling model. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 8171-8172 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Our J. Chem. Phys. 103, 1152 (1995) article described synthetic data generated from the coupling model, which was analyzed in the framework of mode coupling theory (MCT). The purpose was to demonstrate that someone unaware of how the data was generated could carry out an MCT analysis and find some, though not necessarily all, of the features to be in conformance to MCT. The work thus served as a caution against fixation on only some features of short time experimental data, since this can lead to premature conclusions that MCT has been verified. Due to the limitations of experiments on real materials, most data either does not allow a test of all MCT predictions or, as has been found in polymers, is in disagreement with MCT. These points, which have evidently been missed, are reiterated in the present communication. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 4632-4636 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Results of molecular dynamics simulations (MDS) of o-terphenyl, a glass-forming liquid, are analyzed in terms of the coupling model of relaxation. At low temperatures thermally activated relaxation processes are suppressed, whereby the density–density correlation function, C(t), obtained by MDS is determined entirely by vibrational modes. This enables the low temperature data to be used to deduce the vibrational density of states, g(ω). With g(ω) determined, the vibrational contribution, Cpho(t), is calculated at higher temperatures assuming that g(ω) is independent of temperature. At higher temperatures, relaxation makes its appearance and is modeled here by the fast dynamics of the coupling model. Assuming that vibration and relaxation contribute independently, the density–density self-correlation function is given by the product Cpho(t)Crel(t), with the relaxation part obtained from the coupling model. There is good overall agreement between the calculated C(t) and the MDS data. Microscopic parameters, including the energy barrier for reorientation of the o-terphenyl molecule, are extracted from the MDS results. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 4033-4035 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 1152-1159 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Calculations have been presented for the intermediate scattering function, dynamic structure factor, and dynamic susceptibility of a complex correlated system undergoing relaxation with independent vibrations. The vibrational contribution was approximated by a Debye spectrum, smoothed at high frequency, while the coupling model was used to describe the relaxation. This model asserts for nonpolymeric glass-forming liquids a crossover at a microscopic time from intermolecularly uncorrelated relaxation at a constant rate to intermolecularly coupled relaxation with a time-dependent, slowed-down rate. Although the model has previously been employed to successfully predict and otherwise account for a number of macroscopic relaxation phenomena, critical phenomena are not included in, and cannot be addressed by, the coupling model. Notwithstanding an absence of any change in transport mechanism for the supercooled liquid at a critical temperature, the coupling model data, when analyzed in the manner used for mode coupling theory, shows various features interpreted by MCT as critical dynamic singularities. These include an apparent fast "β'' relaxation giving rise to a cusp in the temperature dependence of the Debye–Waller factor, a power-law divergence in the temperature dependence of the relaxation time for the α process, and critical exponents for the relaxation having a defined relationship to one another.Additionally, other experimental features of the short-time dynamics, such as the anomalous Debye–Waller factor and the von Schweidler law, are also observed in results derived from the coupling model. Whatever similarities underlie the coupling model and MCT, a crucial difference is that only the latter predicts the existence of critical phenomena. Yet these and other distinct features are exhibited by the coupling model data. Evidently, any interpretation of short-time behavior in terms of MCT is ambiguous, if not necessarily incorrect. This indicates the importance of the many macroscopic-time relaxation properties found over the years in glass forming liquids (including polymers, small molecule van der Waal liquids, and inorganic materials), and the necessity that they be addressed by any theory, including MCT, purporting to offer a fundamental description of relaxation phenomena.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 2825-2830 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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