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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 159-168 
    ISSN: 0887-624X
    Keywords: nylon 6,6 ; water absorption ; NMR microscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The uptake of water by nylon 6,6 [42DB Adipure (trade name of Dupont Canada Inc.)] at 100°C has been monitored by a combination of one-dimensional proton NMR spectroscopy, relaxation time (T1 and T2) measurements and proton microscopic NMR imaging techniques. The relaxation times of the water absorbed into the nylon matrix are very short at room temperature, (T2 〈 1 ms and T1 ≈ 1 s) indicating that the water is located in a highly restricted environment and suggesting that strong interactions exist between the absorbed water and the polymer. The diffusion profiles measured at room temperature indicate that the diffusion of water into nylon 6,6 at 100°C is Case I Fickian diffusion. The spatial dependence of the T2 relaxation time constant and its variation with the water content was also examined. The results reveal that both T2 and T2* decrease toward the center of the sample in samples that have a concentration gradient of sorbed water. In fully saturated samples, no spatial dependence was observed. The overall values of T2 and T2* are also observed to increase as a function of exposure time. An evaluation of the desorption process at room temperature and at 100°C was performed. A continuous, exponentially decreasing solvent profile was observed for the desorption process which again indicates Case I Fickian kinetics. The exchange process of external bulk and atmospheric water with deuterium oxide (D2O) saturated nylon rods has also been studied using the microscopic imaging technique. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 276-283 
    ISSN: 0749-1581
    Keywords: NMR imaging ; Freezing ; Dimethyl sulphoxide ; Cryoprotectant ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NMR microscopic imaging is shown to be an excellent probe of the freezing and thawing phenomena of liquids in heterogeneous chemical systems, and, in addition, is capable of monitoring the freezing-thawing of mixed solvent systems. In the model mixed solvent system Me2SO-water, the chemical shift specific slice selective (C4S) imaging technique is used to obtain the spatial distributions of the concentrations and mobilities of the two individual solvents in test samples. Measurements of relaxation parameters make it possible to choose values of imaging parameters TE and TR to ensure quantitative reliability of the images. Images of test samples generated at various temperatures demonstrate the qualitative relationship between image intensity and the Me2SO-water phase diagram. This series of experiments verifies that NMR microscopic imaging will be a powerful tool for the study of liquids within solid matrices, and in particular of cryoprotectant solvents in biological systems.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 22 (1983), S. 259-275 
    ISSN: 0570-0833
    Keywords: NMR spectroscopy ; Zeolites ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: After outlining the chemical features and properties which make zeolites such an important group of catalysts and sorbents, the article explains how high-resolution solid-state NMR with magic-angle spinning reveals numerous new insights into their structure. 29Si-MAS-NMR readily and quantitatively identifies five distinct Si(OAl)n(OSi)4-n structural groups in zeolitic frameworks (n = 0, 1,….4), corresponding to the first tetrahedral coordination shell of a silicon atom. Many catalytic and other chemical properties of zeolites are governed by the short-range Si, Al order, the nature of which is greatly clarified by 29Si-MAS-NMR. It is shown that, as expected from Pauling's electroneutrality principle and Loewenstein's rule, both in zeolite X and in zeolite A (with Si/Al = 1.00) there are no —Al—O—Al— linkages. In zeolite A and zeolite X with Si/Al = 1.00 there is strict alternation of Si and Al on the tetrahedral sites. Ordering models for Si/Al ratios up to 5.00 (in zeolite Y) may also be evaluated by a combination of MAS-NMR experiments and computational procedures. 29Si-MAS-NMR spectra reveal the presence of numerous crystallographically distinct Si(OSi)4 sites in silicalite/ZSM-5, suggesting that the correct space group for these related porosilicates is not Pnma. 27Al-MAS-NMR clearly distinguishes tetrahedrally and octahedrally coordinated aluminum, proving that, contrary to earlier claims, Al in silicalite is tetrahedrally substituted within the framework. In combination, 29Si- and 27Al-MAS-NMR is a powerful tool for monitoring the course of solid-state processes (such as ultrastabilization of synthetic faujasites) and of gas-solid reactions (dealumination of zeolites with silicon tetrachloride vapor at elevated temperatures). They also permit the quantitative determination of framework Si/Al ratios in the region 1.00 〈 Si/Al 〈 10 000. Since most elements in the periodic table may be accommodated within zeolite structures, either as part of the exchangeable cations or as building units of the anionic framework, there is immense scope for investigation by MAS-NMR and its variants (cross-polarization, multiple pulse and variable-angle spinning) of bulk, surface and chemical properties. Some of the directions in which future research in zeolite science may proceed are adumbrated.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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