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  • 1
    Online Resource
    Online Resource
    Dordrecht : Springer Science + Business Media, Inc
    Keywords: Chemistry ; Chemistry, Organic ; Chemistry, Physical organic ; Chemistry, inorganic ; Polymers ; Biopolymere ; Cellulose ; Polysaccharide ; Lignin ; Thermodynamische Eigenschaft
    Description / Table of Contents: From the reviews:'...This very well written new book is recommended to academic and industrial researchers and specialists interested in green polymers and mainly in their thermal properties...This new and opportune book covers some important properties of green polymers and bio-composites.' (D. Feldman, Concordia University, Montreal, Canada)
    Type of Medium: Online Resource
    Pages: Online-Ressource , v.: digital
    Edition: Online-Ausg. 2005 Springer eBook Collection. Chemistry and Materials Science
    ISBN: 9781402023545
    Series Statement: Hot Topics in Thermal Analysis and Calorimetry 4
    DDC: 620.192
    RVK:
    Language: English
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  • 2
    Online Resource
    Online Resource
    Dordrecht : Springer Netherlands
    Keywords: Chemistry, inorganic ; Chemistry, Organic ; Chemistry, Physical organic ; Polymers ; Chemistry ; Polymer Sciences
    Description / Table of Contents: Characterization of Green Polymers -- Thermal Properties of Cellulose and its Derivatives -- Polysaccharides from Plants -- Lignin -- PCL Derivatives from Saccharides, Cellulose and Lignin -- Environmentallly Compatible Polyurethanes Derived from Saccharides, Polysaccharides and Lignin -- Bio- and Geo-Composites Containing Plant Materials
    Type of Medium: Online Resource
    Pages: Online-Ressource (XI, 311 p, digital)
    ISBN: 9781402023545
    Series Statement: Hot Topics in Thermal Analysis and Calorimetry 4
    RVK:
    Language: English
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 1655-1668 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Strips of amorphous cellulose film were conditioned under wet atmospheres of 80 and 100% relative humidity or heated at 393 K in vacuo for different time intervals. The structural change of these samples was investigated using differential scanning calorimetry (DSC), IR spectrometry, x-ray diffractometry (x-ray), and the density-gradient column method. In the initial stage of conditioning of cellulose samples at a wet atmosphere, it was found that the thermally determined relative volume fraction (α) of the amorphous part of cellulose stays constant while the diffusion coefficient (Dod), calculated from the rate of H → D exchange of OH groups observed in IR, decreases rapidly. This fact seems to show that the rearrangement of cellulose molecules does not occur as a whole but only partly in the vicinity of the OH groups which affect the process of H → D exchange. If large amounts of water are supplied, however, cellulose molecules rearrange freely and provide a crystalline structure, as observed clearly by x-ray. On the other hand, during the heat-treatment of amorphous cellulose, the decrease of α and Dod can be clearly observed by DSC and IR from the initial stage of treatment. Judging from the change of α and Dod, it was inferred that the hydrogen bond formation occurs step by step simultaneously with the rearrangement of cellulose molecules by heat-treatment.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 1265-1274 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The amounts of three different types of water adsorbed on hydrolyzed lignin, which was obtained by acid hydrolysis of softwood meal in 1,4-dioxane containing trace amounts of hydrochloric acid (in the following called DL), and on its derivatives, i.e., methylated and acetylated lignins, were determined by differential scanning calorimetry (DSC). The first type of water is non-freezing water, the glass transition of which was detected by DSC. The second type of water corresponds to a kind of bound water which was detected from a crystallization peak in the vicinity of 225 K (peak II). This peak appeared when the water content exceeded a critical amount of non-freezing water. The third type of water is free water, the crystallization peak (peak I) of which was found at the same temperature as that of pure water. From the enthalpies of crystallization of the above two types of water and the known weight of sorbed water, the amount of bound water in DL was determined to be 0,10 (weight of bound water/weight of dry sample). Furthermore, it was found that bound water breaks hydrogen bonds in DL and decreases its glass transition temperature (Tg) from 425 K to 330 K. The amount of hydroxyl groups, which varies with the degree of methylation or acetylation, was also found to affect the bound water content and inevitaby to decrease T g.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 1875-1884 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phase transition of water sorbed in regenerated cellulose (II), for water contents ranging from 0 to 1,0 (water/dry cellulose, g/g), was investigated by differential scanning calorimetry (DSC). It was found that the amount of water bound to each glucose unit is ca. 3 mol considering that water diffuses only into the amorphous region of cellulose. The increase of this amount by adding excess water to cellulose suggests that the amorphous region of cellulose II increases in the presence of water. The transient state, at a water content ranging from 0,4 to 0,6, where the intermolecular distance expands, is reflected in an intermediate crystallization at a temperature between the crystallization of free water and freezing bound water. Mechanical properties of cellulose II under moist conditions were related to the results obtained by DSC. Further, the strength at break of cellulose II was compared with that of natural cellulose (I). The strength of cellulose II decreases in presence of bound water, whereas that of cellulose I increases. Based on the comparison of the results of DSC and mechanical properties of cellulose I and II, the difference is attributed to the structural change of the amorphous region when water molecules are bound to the hydroxyl groups of cellulose. The defect or internal strain of the amorphous region of cellulose I decreases and the molecular chain is transformed into a more regular arrangement when water molecules break hydrogen bonds. On the other hand, the amorphous chain of cellulose II takes a more released and expanded arrangement in presence of water molecules which break hydrogen bonds in the crystalline region of cellulose II. The decrease of crystallinity was observed by x-ray diffraction.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 196 (1995), S. 99-113 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The formation of freezing water as a function of temperature and time has been studied in polyelectrolytes and in cellulose. In such systems, a portion of the sorbed water is not crystallizable under normal conditions. However, it was observed that in rapidly cooled systems the ratio between freezing and non-freezing water is variable and depends on the annealing temperature. The difference between the saturated concentration of freezable water and the concentration of freezing water which is formed immediately after the rise of the sample's temperature is dependent on the materials geometry. It is assumed that the rise of the annealing temperature above room temperature increases the amount of mobile water which can crystallize. By comparing the measured concentration of freezing water with desorption analysis, the average distance of transportation of mobile water for sodium carboxymethylcellulose was calculated as 8-10 μm.
    Additional Material: 10 Ill.
    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 40 (1990), S. 657-667 
    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: The dynamic viscoelasticity was investigated for isoprene rubber (IR) composites filled with untreated and chemically treated cellulose fibers. Mercerization and benzylation were employed as chemical treatments. Bleached kraft pulp and cellulose powder were used as cellulose fillers. By mixing cellulose fillers, the dynamic modulus E′ of IR composites was improved, especially above the glass transition temperature. Benzylation of cellulose fibers reduced E′ of IR composite, while mercerization increased it. A tan δ peak was observed at about -33°C at 110 Hz along with a shoulder peak at about -16°C for the IR composites. The intensity of the tan δ peak decreased when mixed with cellulose fillers. The shoulder peak next to the main peak could be separated assuming a Gaussian type equation; log E″ = D exp { -C[(1sol;T) - (1/T0)]2} where D is the maximum value of log E″ vs. 1/T curve, T0 is the maximum temperature, and C is a parameter to determine the width of the Gaussian function. From the Arrhenius plot of the frequencies against 1/T0, the apparent activation energies were calculated as 220-235 kJ/mol for the shoulder peak (α1 process) and ca. 180 kJ/mol for the main peak (α2 process). The α2 process is caused by the glass transition of the rubber matrix. The α1 process is assigned as the molecular motion of the rubber matrix strongly restricted by the fiber element.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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: Polyurethane films were prepared by solution casting using a three-component system consisting of polymeric MDI, a propylene oxide-based polyether triol and kraft lignin fractions of different molecular weights. The polyether triol was used as soft segment. The composition of the polyurethanes was varied whereas the NCO/OH ratio was kept constant. The crosslink density increased with increasing molecular weight of the kraft lignin fraction used, which is a result of an increase in functionality of the kraft lignin with increasing molecular weight. Polyurethanes prepared from low molecular weight kraft lignin were found to be more flexible than those prepared from medium and high molecular weight kraft lignin (at lignin contents below 30%). At kraft lignin contents higher than about 30% (which at the NCO/OH ratio used corresponds to a hard segment content of about 70%), rigid and glassy polyurethanes were obtained regardless of the molecular weight of the kraft lignin fraction used.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 9
    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: Polyurethane (PU) films were prepared by solution casting using a three-component system consisting of a low molecular weight fraction of softwood kraft lignin (KL), polyethylene glycol (PEG) of various molecular weights, and crude diphenylmethane diisocyanate (MDI) as starting materials. All films were prepared using a constant NCO/OH ratio. The effects of KL content, PEG content, and molecular weight of PEG on the tensile, thermal, and swelling properties of the PUs were studied. The results showed that the crosslink density Tg and tensile properties were essentially unaffected by variations in the sequence length of the soft segment at a given PEG content. The properties of the PUs were found to depend mainly on the soft/hard segment ratio. The behavior of the glass transition temperature upon changes in the PU composition indicated that the soft and hard segments were extensively mixed.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 198 (1997), S. 883-898 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential scanning calorimetric (DSC) studies were carried out for hydrophobically modified hydroxyethylcellulose (HMHEC)- and hydroxyethylcellulose (HEC)-water systems to examine the binding of water with polymer molecules and the formation of a structure. The amount of freezing-bound water in HMHEC was found to be much less than that in HEC. The above fact suggests that the water-polymer interaction is hindered by the presence of the hydrophobes. The formation of a structure above the melting point of ice was detected by DSC for both systems HMHEC- and HEC-water. Polarizing light micrographs of these two aqueous polymer systems showed the formation of a liquid crystalline state in the same range of temperature. These phenomena were observed in a wider range of water content for HMHEC (Wc 〈4.0) than for HEC (Wc 〈2.5).
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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