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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1677-1696 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Effect of extrusion conditions, particularly temperature, on the structure development of fibers from poly(ethylene terephthalate) modified with 60 mol% p-hydroxybenzoic acid was investigated. Light microscopy revealed that the structure of the liquid-crystalline fiber was highly dependent on the extrusion temperature: low-temperature-spun fibers exhibited a structure with domains or clusters of crystallites randomly oriented, whereas the fibers spun at high temperatures had a well-developed fibrillar texture. Anisotropy of the fibers, as evidenced by dichroism and by the variation of brightness or darkness of the fibers between crossed polars, was significantly higher for those spun at relatively high temperatures. Scanning electron microscopy revealed that the fibers spun at relatively low temperatures had poorly oriented, nonuniform morphology. Those produced at relatively high temperatures, on the other hand, consisted of well-developed fibrils. X-ray diffraction patterns showed that the molecular orientation increased with increasing extrusion temperature. A model for the development of fiber structure from thermotropic liquid-crystalline polymers is proposed.
    Additional Material: 17 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 3469-3481 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissolution of cellulose in solutions of liquid ammonia and ammonium thiocyanate is discussed. Viscosity measurements on dilute solutions of cellulose in this solvent over a range of shear rates and shear stresses are reported. A four-bulb Ubbelohde suspended level viscometer was used for the measurements. Plots of log [η] versus log M gave Mark-Houwink coefficients of a = 0.95 and K = 6.686 × 10-5 at 25°C for [η] as dl/g. The Bloomfield equation was used to calculate effective bond lengths (b) from limiting viscosity numbers of cellulose in solutions of ammonia/ammonium thiocyanate and Cuene, respectively. Results indicate that cellulose may have similar configurations in both solvents and also that the ammonia solutions are true cellulose solutions. Miscibility of the cell- ulose/ammonia/ammonium thiocyanate solutions with organic solvents, such as glycerol, is also reported. Further, a few interesting characteristics of the liquid ammonia/ammonium salt solutions, discussed briefly, are the convenient boiling point, the rheological behavior, and the relatively high concentration of cellulose obtainable.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 651-670 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissolution process and some solution properties of cellulose in mixtures of liquid ammonia (NH3) and ammonium thiocyanate (NH4SCN) are discussed. The mole fraction ratio of NH3, NH4SCN, and H2O which dissolve cellulose were determined. The effect of temperature on several solution properties was also examined. The temperature coefficient d In [n]/dT for the limiting viscosity number [n] has a value of -1.58 × 10-2 °C-1. This is considered to be rather large but is, in fact, a common occurrence for almost all cellulose derivatives in solution. The values for the Huggins constant K′ showed no systematic trends with temperature. They did, however, suggest the presence of considerable association of the cellulose in solution. Miscibility results of adding the cellulose solutions to organic liquids are also reported.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1511-1520 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: A high molecular weight polyethylene terephthalate was spun into fibers in the speed range from 3,000-7,000 mpm. The effect of modifying threadline dynamics through a combination of enhanced and/or retarding air quenches on the resulting spinning performance, fiber structure, and mechanical properties was examined. Particular combinations of these threadline temperature profile modifications were shown to result in significant improvements in spinning performance and as-spun fiber structure. Extensive characterization of select fiber samples revealed higher orientation and crystallinity, larger crystal dimensions, and greater mechanical properties. These results also demonstrated the ability to provide continued improvement in fiber properties at very high take-up speeds where typically a decline is observed. It is concluded that the threadline temperature profile can be altered in such a way as to significantly enhance the resulting spinning performance and fiber structure over a wide range of take-up speeds.
    Additional Material: 11 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 445-448 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Cellulose xanthate solutions with α-cellulose content from 9 to 14% were obtained and their properties were examined. It has been found that viscoses containing urea are more stable and possess lower viscosity as compared with conventional viscoses. Properties of fibers obtained from viscoses with increased α-cellulose content were discussed. It has also been found that such fibers show higher linear density and their tensile strength depends on the α-cellulose content in the viscose.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 673-680 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C-NMR chemical shifts of a cellulose with a DPw of 23 dissolved in the NH3/NH4SCN solvent system were found to be very similar to those of cellulose dissolved in DMSO (cellulose oligomers), in the LiCl/DMAC system and in the N-methylmorpholine N-oxide/DMSO system. It was concluded from this that cellulose does not react with the NH3/NH4SCN solvent. It was found, however, that glucose reacts with the solvent at C-1 to form β-D-glucopyranosy-lamine. Separation of this compound from the solvent resulted in another compound which was determined to be β,β-di-D-glucopyranosylamine. The compounds β-D-glucopyranosylamine, N-acetyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylamine, β,β-di-D-glucopyranosylamine, α,β-di-D-glucopyranosylamine, 2,3,4,6,2′,3′,4′,6′-octa-O-acetyl-α,β-di-D-glucopyranosylamine were all synthesized and the 13C-NMR chemical shifts of these compounds are reported. It was also found that for the low-DP cellulose sample which was used the reducing end group existed and had reacted with the solvent to form an amine at C-1.
    Additional Material: 14 Ill.
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  • 7
    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.
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  • 8
    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.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 547-556 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This article reports the use of classical light scattering to study cellulose in the NH3/NH4SCN solvent system. Three solvent compositions were used, 27.01 73.0,25.5/ 74.5, and 24.51 75.5 weight ammonia/weight ammonium thiocyanate. The coefficient, (dn/dc)υ, was determined by back calculating using the molecular weight determined by solution viscometry in the solvent system cupriethylenediamine and the classical light-scattering results. Second virial coefficients were found to be similar to those values measured for cellulose in the FeTNa and LiCl/DMAC solvent systems. The characteristic ratios were found to vary with solvent composition with the highest values being at a composition of 25.5/74.5 weight ammonia/ weight ammonium thiocyanate. Persistence lengths were also found to vary with solvent composition with the highest value being 264 × 10-8 cm at solvent composition 25.5/74.5.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 557-563 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This is the second part of a two-part study of the NH3NH4SCN cellulose solvent system. Quasielastic light scattering was used to determine the diffusion coefficients of cellulose in solution and the effective hydrodynamic radius of the dissolved molecules. Additionally, the system was studied using light microscopy to determine the minimum critical volume fraction or liquid crystal formation. Very little change was found in the diffusion coefficients with change in cellulose concentration indicating little interaction between the chains in solution. Values of 7.69 and 2.66 × 108 cm2/s were measured for samples having a degree of polymerization of 153 and 969. The value of the coefficient relating the hydrodynamic volume to the radius of gyration was found to be in the range of 0.33 to 0.53, indicating an extended coil conformation according to the Kirkwood-Riseman theory. The minimum critical volume fractions necessary for liquid crystal formation, υ2′ were 0.039, 0.038, and 0.048 for the three solvent compositions studied. The values calculated for υ2′ based on the measured persistence lengths were much larger than the predicted values, indicating strong deviation from theory or possible aggregation in the system.
    Additional Material: 2 Ill.
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