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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 3196-3198 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 24 (1991), S. 759-770 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-882X
    Keywords: Acetobacter xylinum ; native band cellulose ; agar plate medium ; high viscous medium ; cell motion ; physical constraints
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Acetobacter xylinum, which normally produces ribbon-like microfibrils of cellulose I, occasionally synthesizes a band-like cellulose (native band, or NB) having a cellulose II crystal structure with a putative folded-chain structure. In contrast to a previous finding of NB production by a mutant strain of A. xylinum, we found that the wild-type strain also produced NB when incubated on agar plate medium. Incubation of the same strain in liquid media of varying viscosity with the addition of polyethylene glycol (PEG) resulted in the production of normal ribbon at low viscosities and NB at high viscosities. This behaviour was independent of the molecular weight of PEG and there seemed to be a critical level in viscosity for the switching from ribbon production to NB production. These findings strongly suggest that NB production is induced by a low mobility of cells in the culture medium due to physical constraints.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellulose 4 (1997), S. 75-87 
    ISSN: 1572-882X
    Keywords: bacteria, cotton linter ; mercerization ; acidhydrolysis ; leveling-off degree of polymerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Structural changes in never- dried, disintegrated bacteria l cellulose by treatment with aqueous NaOH were examined by electron microscopy, X-ray diffractometry and acid hydrolysis behaviour and compared with those of cotton cellulose. The microfibril kept its fibrillar morphology after treatment with NaOH solutions of less than 9% (w/w), but changed into irregular aggregates when treated with NaOH above 12% (w/w), corresponding to the crystal conversion to cellulose II. The crystallinity of the resulting cellulose II was very low after a brief alkali treatment, but was increased significantly by elongated treatment (up to 10 days). In contrast, cotton cellulose was converted to cellulose II of fairly high crystallinity by alkali treatment of as little as 3 min duration, and the crystallinity did not change with longer treatments. The leveling-off degree of polymerization (LODP) of bacterial cellulose was decreased from 150 to 50 by 18% (w/w) NaOH treatment, while that of cotton linter decreased from 260 to 70. These characteristic differences between cotton linter cellulose and bacterial cellulose can be ascribed to a basic difference in microfibrillar organization in these materials: the microfibrils in cotton cellulose are in close contact with neighbouring microfibrils having opposite polarity, and in bacterial cellulose are isolated from each other and require chain folding to form the antiparallel cellulose II crystal
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cellulose 4 (1997), S. 221-232 
    ISSN: 1572-882X
    Keywords: two crystalline phase system ; synchrotron radiated X-ray diffraction ; time-of-flight neutron diffraction ; cellulose Iα ; cellulose Iβ
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Precise determination of d-spacings and compositional ratio of cellulose Iα and Iβ in various native cellulose samples was successfully carried out by synchrotron-radiated X-ray diffraction and time-of-flight (TOF) neutron diffraction from quasi-powder specimens. X-ray diffraction peaks were separated by the deconvolution method using six types of profile function: Gaussian, Lorentzian, intermediate Lorentzian, modified Lorentzian, pseudo-Voigt, and Pearson VII. In terms of R-factors, the pseudo-Voigt function gave the best fit with the observation, and was used for determination of d-spacings. The numerical results for Valonia cellulose were: dIα (1 0 0) = 0.613 nm; dIβ (1 1 0) = 0.603 nm; dIβ (1 1 0) = 0.535 nm; dIα (0 1 0) = 0.529 nm; Iα content = 0.65. The differences determined between dIα (1 0 0) and dIβ (1 1 0) and between dIβ (1 1 0) and dIα (0 1 0) were similar to those previously reported. Comparison between unresolved peaks for the two types of cellulose samples revealed a small but definite difference between dIα (1 1 0) and dIβ (2 0 0). The TOF neutron diffractometry using deuterated samples confirmed this difference.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-882X
    Keywords: wood cellulose ; two crystalline phase system ; CP/MAS13C NMR ; FT-IR ; electron diffraction ; X-ray diffraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract We have investigated unlignified tension wood and normally lignified wood celluloses inPopulus maximowiczii with particular reference to the composition of two crystalline phases Iα/Iβ (triclinic/ monoclinic). Four independent techniques, which enable us to detect the two phases, CP/MAS13C NMR, Fourier transform infrared microscopy, selected-area electron diffraction, and X-ray diffraction were applied. Because of the low crystallinity of wood celluloses, particularly in the case of celluloses in the lignified cell wall, no single method was decisive enough to be able to determine the composition of the two phases as one can with highly crystalline materials. The Iβ dominant structure (monoclinic crystal type) was, however, preferred for both tension and normal wood celluloses.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1491-1496 
    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 survey by X-ray diffractometry was carried out to confirm the two crystalline phase Iα/Iβ(triclinic/monoclinic) system of native celluloses. We have investigated cellulose samples from 12 different origins and measured the d-spacings with reasonable precision. The samples were then subjected to the hydrothermal annealing that brings the cellulose crystals to the monoclinic type; d-spacings were reevaluated afterward. From the statistical analysis using observed d-spacings, all the cellulose samples were categorized into the two groups that coincide with the two crystalline phase systems: one is the algal-bacterial type rich in triclinic phase and the other is the cotton-ramie type of the monoclinic phase. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of wood science 44 (1998), S. 73-77 
    ISSN: 1611-4663
    Keywords: Heat treatment ; Vibrational properties ; Crystallization ; Atmospheric condition ; Temperature-time condition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Sitka spruce (Picea sitchensis Carr.) wood was heated for 0.5–16.Oh at temperatures of 120°–200°C in nitrogen gas or air. The values for Young's modulus, shear modulus, and loss tangent were measured by free-free flexural vibration tests. X-ray diffractometry was carried out to estimate the crystallinity index and crystallite width. The results obtained are as follows: (1) Density decreased at higher temperatures and longer heating times. The specific Young's modulus, specific shear modulus, crystallinity index, and crystallite width increased during the initial stage and were constant after this stage at 120°C and 160°C, whereas they increased during the initial stage and decreased later when the temperature was high. Loss tangent in the longitudinal direction increased under all conditions, whereas that in the radial direction increased at 120°C and decreased at 160°C and 200°C. (2) From the relation between Young's modulus and moisture content, it can be safely said that Young's modulus is increased by the crystallization and the decrement in equilibrium moisture content, and that crystallization (rather than degradation) is predominant at the initial stage of the heat treatment, whereas the latter is predominant as the heating time increases. (3) It is implied that the specific Young's modulus, specific shear modulus, crystallinity index, and crystallite width decreased more in air than in nitrogen gas because of oxidation in air.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of wood science 44 (1998), S. 310-313 
    ISSN: 1611-4663
    Keywords: Cellulose ; Mercerization ; Ramie ; Swelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Morphological changes of ramie fibers due to swelling in alkali solution were investigated. The observed twisting and changes in the cross-sectional shape of the fibers could be explained as a geometrical alteration caused by lateral expansion of coiling fibrils, as the unmercerized ramie fiber showed an S-helix structure. The fibril angle of ramie fibers was estimated to be 3°. Although the swollen fiber untwisted to some extent on washing with water, the shape of the twisted ribbons as observed by scanning electron microscopy was retained even after drying. Concentrated 8N NaOH produced only a moderate change in morphology, whereas swelling with 3.5N NaOH at 0°C expanded the cross sections about 30 times over the initial ones accompanied by a drastic change in the shape of the fiber.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of wood science 45 (1999), S. 258-261 
    ISSN: 1611-4663
    Keywords: Cellulose microcrystal ; Sulfate ester ; Surface charge ; Viscosity behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Microcrystalline cellulose with minimal surface charge was prepared from softwood kraft pulp via hydrolysis by 4N hydrochloric acid instead of sulfuric acid. To this material, sulfate ester groups as surface charge were introduced by treating with 55% (w/w) sulfuric acid. A treatment at 60°C for 2h gave nearly the same level of surface charge as that of the H2SO4 -hydrolyzed microcrystal. The number of sulfate groups were controlled by changing the H2SO4 treatment conditions. Although the microscopic size and shape of the microcrystalline particles were the same irrespective of the preparation method, the introduction of surface charge drastically reduced the viscosity and removed its time dependence. These changes in viscosity behavior are considered to result from charge-induced dispersion of loose aggregates existing in the initial charge-free microcrystals prepared by HCl hydrolysis.
    Type of Medium: Electronic Resource
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