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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 9174-9178 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Segment diffusion in a polyethyleneoxide melt (Mw = 5 000 000) was studied with the aid of the supercon fringe field version of field-gradient NMR diffusometry. The evaluation based on the second moment of the probability density function, i.e., the mean squared displacement, shows reasonable agreement with the predictions of the tube/reptation model. However, taking into account the whole probability density function, leads to substantial discrepancies. © 1996 American Institute of Physics.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 2247-2250 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Liquids filled in porous media such as porous glass do not freeze at the bulk freezing temperatures. Two phases must be distinguished. A one to at most two monolayer thick film adsorbed on the inner surfaces does not freeze at all, whereas free liquid within the pores freezes at reduced temperatures relative to the bulk values as predicted by the Gibbs/Thompson equation. The fraction of non-freezing liquid can be evaluated from the reduction factor of the low-frequency spin-lattice relaxation time upon freezing of the free liquid. A method for the determination of the pore size may be established on this basis. Water and tetradecane, i.e., a polar and a nonpolar adsorbate, filled in porous glass have been studied with the aid of field-cycling nuclear magnetic resonance (NMR) relaxometry. Above the freezing range the frequency dependences of the spin-lattice relaxation time T1 of the two liquids strongly deviate from each other owing to the different adsorption properties. On the other hand, with frozen samples the same frequency dependence of the liquid phase, that is essentially T1∝ν0.67, was found with both adsorbates. This proves that a nonpolar liquid confined to a thin layer on a polar surface underlies an equivalent relaxation mechanism as a strongly adsorbed polar liquid. As the dominating process, reorientations mediated by translational displacements along the curved and rugged surface are considered. © 1995 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 365-370 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A NMR method is presented which permits one to probe order fluctuations in ordered materials such as nematics. Information on the order parameter is also accessible. The principle is based on the standard stimulated-echo three-pulse sequence. Both the stimulated and the primary echo are recorded. The quotient of the echo amplitudes is measured as a function of the spacing of the first two rf pulses. The attenuation curves of the quotient corrected for spin-lattice relaxation show strong modulations directly reflecting the order parameter of the material. This dipolar-correlation effect moreover provides information on the distribution of the director fluctuation modes. The time scale exceeds the millisecond range by far. A formalism has been developed which permits us the quantitative description of experimental data measured in nematic 5CB. © 1995 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 3301-3306 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dipolar-correlation effect on the stimulated echo of nematics probes (a) the order parameter and (b) the distribution of the director fluctuations. This effect was employed for the study of orientational director fluctuations in a nematic liquid crystal confined in Bioran porous glasses with mean pore diameters of 30, 70, and 200 nm. No macroscopic preferential orientation of the director could be detected in the confined material. The reason is, that the local director is oriented by surface interactions rather than by the magnetic field. As already shown in our previous work, the attenuation of the dipolar correlation quotient (stimulated-echo amplitude divided by the primary echo amplitude) is able to monitor director fluctuations in the time scale of the pulse sequence. The echo attenuation rate exhibits a strong dependence on the pore size. It is determined by the mean squared fluctuation of the dipolar coupling constant and characterises the distribution of the director fluctuation modes. The mean squared fluctuation decreases with decreasing pore size. The dependence on the inverse pore diameter decays exponentially and suggests a critical mean pore size of about 120 nm for the crossover to bulk behavior. The dipolar-correlation effect thus may be suitable for the determination of mean pore diameters in porous materials. © 1996 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 6929-6939 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Diffusion of adsorbate molecules along surfaces of porous media was examined with respect to ordinary and Lévy walk diffusion mechanisms. The orientational structure factor formalism of the "reorientation mediated by translational displacements" (RMTD) mechanism originally derived for ordinary diffusion is generalized to Lévy walks. The two cases can be distinguished experimentally using field-cycling NMR relaxometry. The low-frequency spin-lattice relaxation dispersion is influenced by the dynamics on the surfaces as well as by the surface geometry. The experiments were carried out with polar and nonpolar liquids filled into porous glasses and fine particle agglomerates (ZnO, TiO2). The spin-lattice relaxation dispersion of polar and nonpolar adsorbate species shows dramatic differences, and reflects the limits of "strong" and "weak" adsorption, respectively. The low-frequency behavior is explained by RMTD along the surfaces. At temperatures below the freezing point of the confined liquids, one or two molecular diameter thick surface layers remain unfrozen. Molecular dynamics in the interfacial liquid in these nonfreezing surface layers (NFLs) were also studied. The propagators relevant for RMTD are shown to depend on whether the sample is frozen or not. In the NFL case, an ordinary Gaussian displacement distribution function applies, whereas a Lévy walk surface diffusion process with a Cauchy distribution tends to dominate in the strong-adsorption limit. On a much longer length scale beyond the so-called retention time when diffusion becomes normal, field gradient NMR diffusometry was applied. Confinement of the liquid adsorbate to the pore space or, in frozen samples, to the NFL reduces the diffusion coefficient mainly due to the geometrical restriction. In the case of NFLs, the reduction amounts to one order of magnitude relative to the bulk values. © 1998 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 6501-6509 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: NMR (nuclear magnetic resonance) nutation is treated with respect to demagnetizing-field effects on the evolution of spin coherences. A two-dimensional NMR nutation spectroscopy scheme is suggested consisting of a single radio frequency (RF) pulse and a free-evolution period. The RF pulse amplitude as well as the external magnetic field are assumed to be subject to gradients in the same but otherwise arbitrary direction. Cross peaks are predicted as frequency domain counterparts of multiple echoes. It is suggested to analyze the cross peak shape in terms of distributions of internal gradients arising from magnetic susceptibility inhomogeneities in heterogeneous samples. Furthermore, a pulse scheme solely based on gradients of the RF amplitude is treated resulting in the prediction of multiple rotary echoes as counterparts to the conventional rotary echo. The origin again is evolution in the presence of spatially modulated longitudinal magnetization in the tilted rotating frame. © 1999 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 3708-3713 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In recent years evidence was presented that two radio frequency pulses in combination with suitably matched field gradient pulses produce cross peaks in two-dimensional NMR spectroscopy that reveal all the features of multiple-quantum/single-quantum coherence transfer signals. This experiment was termed CRAZED by Warren et al. Quite amazingly, identical signals were predicted on a purely classical basis. Thus the intriguing question arises whether this means that a classical analog to multiple-quantum coherences exists. In this study we show that this is clearly not the case. Coherence pathways of a purely single-quantum basis are excited anyway and lead independently to superimposed identical signals in parallel. Moreover, the observation of CRAZED signals per se neither disproves the adequacy of the high-temperature approximation, which was questioned in this context, nor proves a strong influence of intermolecular multiple-quantum coherences. However, the indispensable prerequisite for the description of the manifold CRAZED phenomena is that long-range dipolar interactions are taken into account either explicitly or in the continuous-limit form. © 1999 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 846-854 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Chain dynamics in a series of styrene-butadiene rubbers (SBR) was studied with the aid of the dipolar correlation effect (DCE) and field-cycling NMR relaxometry (FCR). The typical time scales of the two techniques are t〉10−4 s and t〈10−3 s, respectively, and therefore complementary. The crosslink density of the polymer networks was varied in a wide range. In order to prevent sinusoidal undulations of the stimulated-echo attenuation curves due to spin exchange between groups with different chemical-shift offsets, the DCE of the samples was examined using a modified radio frequency pulse sequence with additional π pulses inserted in the free-evolution intervals. Residual dipolar couplings can thus be probed in samples where chemical-shift and dipolar interactions are of the same order. The dipolar correlations probed with the DCE in SBR networks turned out to exist on a time scale exceeding 300 ms. The short-time fluctuations (probed by FCR) and the long-time dynamics (probed by DCE) can be approached by power-law dipolar correlation functions with exponents −0.78±0.02 and −1.5±0.1, respectively. The crossover time is in the order of 1 ms. In contrast to FCR, the DCE data strongly depend on the crosslink density but not on the temperature in a range from 30 to 80 °C. On this basis determinations of the crosslink density may be possible as an alternative to the usual mechanical torsion modulus measurements. © 1998 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 6977-6981 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Aqueous suspensions of synthetic saponite clays have been studied using field-cycling NMR relaxometry. The saponite platelets form planar surfaces on which water molecules are adsorbed. As the strong-adsorption limit applies, "bulk mediated surface diffusion" as originally suggested by Bychuk and O'Shaughnessy is expected to occur. That is, within the so-called retention time, adsorbate molecules tend to perform Lévy walks along the surfaces. A corresponding formalism (the "pancake model") is derived and compared with the experimental data. The low-frequency spin-lattice relaxation dispersion can perfectly be described on this basis. The platelet diameter can be estimated from the peculiar adsorbate dynamics on the surfaces in accordance with literature data. © 1999 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 9883-9888 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Based on theoretical considerations [N. F. Fatkullin, Sov. Phys. JETP 72, 563 (1991)], immaterial spin diffusion mediated by flip–flop transitions of dipolar coupled spins on different macromolecules was predicted to influence the diffusion coefficient measured in nuclear magnetic resonance field-gradient experiments. In order to test this hypothesis, we have carried out supercon fringe field proton magnetic resonance diffusometry experiments with polyethylene oxide melts (Mw=438 000) using field gradients of up to 60 T/m. The polymer chains were dispersed in a matrix of deuterated chains of an equivalent molecular mass. The time-dependent segment diffusion coefficients measured in the diluted and undiluted polymer coincided for diffusion times below about 200 ms. However, increasing the diffusion time up to 1 s leads to a reduction of the diffusion coefficient in the deuterated matrix by a factor of about 2 relative to the undeuterated system. The long-time diffusion coefficient measured with long polymer chains, which are subject to interchain spin couplings, is obviously strongly influenced by spin diffusion mediated by flip–flop transitions of dipolar coupled spin pairs. This holds true in spite of the relatively long flip–flop time, which is estimated to be of the order 0.1 s. © 1997 American Institute of Physics.
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