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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 241-247 
    ISSN: 0887-624X
    Keywords: ammonia/ammonium thiocyanate solvent ; cellulose ; dissolution mechanism ; conformation ; swelling ; mercerization ; hydrogen bonding ; entropy ; enthalpy ; affinity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a previous article,1 we reported on the interaction of cellulose with NH3/NH4SCN by using solid state CP / MAS 13C-NMR, wide-angle X-ray and other techniques. It appears that during an imposed temperature cycling sequence, specific cellulosic inter- and intramolecular hydrogen bonds are broken as polymorphic conversion and, ultimately, dissolution occurs. Cellulose is converted from the polymorph I to II to III and, finally, to amorphous. We speculate that these changes proceed via transformation of the polymorph conformations of CH2OH from trans-gauche, “tg,” to gauche-trans, “gt,” to gauche-gauche, “gg.” Remarkably, the temperature cycling effectively and rapidly effects these changes, seemingly, by invoking at two different temperatures (22°C and -78°C), a subtle but powerful temperature-related interplay of enthalpic and entropic forces. At the higher of the cycling temperature limits, entropy and van der Waals forces dominate, causing NH3 to partition in favor of the liquid phase. At the lower of the temperature cycling limits, enthalpy dominates and the situation is reversed favoring NH3 partition toward the cellulose, resulting in breakage of inter- and intracellulosic H-bonds by the interpenetrating ammonia to form new H-bonds between cellulose and ammonia, leading ultimately to conformational changes and, ultimately, even dissolution. © 1994 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 229-239 
    ISSN: 0887-624X
    Keywords: ammonia/ammonium thiocyanate solvent ; cellulose ; dissolution mechanism ; solid state CP/MAS 13C-NMR ; X-ray ; conformation ; hydrogen bonding ; ammonia mercerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ammonia/ammonium thiocyanate (NH3/NH4SCN) is an excellent swelling agent and solvent for cellulose, even at a high degree of polymerization. Because polymorphic conversion in cellulose has been a long-standing, perplexing, troublesome problem, we have undertaken to study that mechanism. Solid state CP/MAS 13C-NMR and X-ray analysis proved to be very useful analytical techniques for the task. It appears that during temperature cycling, specific cellulosic inter- and intramolecular hydrogen-bonds are broken as polymorphic conversion proceeds sequentially from the polymorph I to III, and finally at total solvation to amorphous. This proceeds correspondingly via transformation of the polymorph conformations of CH2OH from trans-gauche, “tg,” to gauche-trans, “gt,” to gauche-gauche, “gg.” © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2209-2222 
    ISSN: 0887-6266
    Keywords: poly(1-trimethylsilyl-1-propyne) ; poly(1-phenyl-1-propyne) ; blends ; gas and vapor transport ; NMR ; Maxwell model ; Bruggeman model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Pure gas and hydrocarbon vapor transport properties of blends of two glassy, polyacetylene-based polymers, poly(1-trimethylsilyl-1-propyne) [PTMSP] and poly(1-phenyl-1-propyne) [PPP], have been determined. Solid-state CP/MAS NMR proton rotating frame relaxation times were determined in the pure polymers and the blends. NMR studies show that PTMSP and PPP form strongly phase-separated blends. The permeabilities of the pure polymers and each blend were determined with hydrogen, nitrogen, oxygen, carbon dioxide, and n-butane. PTMSP exhibits unusual gas and vapor transport properties which result from its extremely high free volume. PTMSP is more permeable to large organic vapors, such as n-butane, than to small, permanent gases, such as hydrogen. PPP exhibits gas permeation characteristics of conventional low free volume glassy polymers; PPP is more permeable to hydrogen than to n-butane. In PTMSP/PPP blends, both n-butane permeability and n-butane/hydrogen selectivity increase as the PTMSP content of the blends increases. © 1996 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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