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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 749-758 
    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: Differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were used to characterize the morphology of solvent cast hydroxypropyl cellulose (HPC) films. DSC results were indicative of a semicrystalline material with a melt at 220°C and a glass transition at 19°C (T1), although an additional event was suggested by a baseline inflection at about 80°C (T2). Corresponding relaxations were found by DMTA. A secondary relaxation at -55°C was attributed to the interaction between hydroxyl groups of the polymer and residual diluent. The tan δ peak at T2 was found to arise from an organized phase, presumably from a liquid-crystal mesophase formed while in solution. Crosslinking with a diisocyanate increased the peak temperature of the two primary relaxations, and resulted in a more clearly defined peak for the T2 transition. From this behavior it was concluded that both T1 and T2 are similar to glass transitions (Tg's) associated with an amorphous component and a more highly ordered phase (due to a residual liquid crystal superstructure) in the HPC bulk.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 759-772 
    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 series of polyurethane (PU) films was prepared from chain-extended hydroxypropyl lignins (CEHPL). In appearance, these films ranged from brittle and dark brown to rubbery and bronze. The thermal, mechanical, and network properties of these PUs were investigated by DMTA and DSC analysis. All films exhibited single Tg's which varied between -53° and 101°C, depending on lignin content. From swelling experiments, molecular weight between crosslinks (Mc) was determined and found to vary over 2.5 orders of magnitude. The Mc's were related to the change in Tg that accompanied network formation. Stress-strain experiments showed a variation in Young's modulus between 7 and 1300 MPa. Most of the variation in material properties was related to lignin content and to a lesser extent to diisocyanate type, hexamethylene diisocyanate, or toluene diisocyanate. The source of the CEHPL had no effect on the observed properties. From these results it was concluded that the properties of PUs can be controlled and engineered for a wide variety of practical uses.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 21 (1979), S. 1679-1683 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1145-1161 
    ISSN: 0887-6266
    Keywords: cellulose ester fibers spun from liquid crystalline solutions ; liquid crystalline solutions of cellulose acetate/butyrate, morphology of fibers spun from ; morphology of cellulose acetate/butyrate fibers spun from liquid crystalline solutions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fibers were spun from isotropic and anisotropic dimethylacetamide solutions of cellulose esters. Take-up speeds of the dry jet/wet spinning process varied. Water served as the coagulant. The mechanical properties of the fibers increased as spinning progressed from the isotropic to the anisotropic state of the solution. A trade-off in solubility and fiber properties was noted as the butyryl acetyl ratio decreased. Whereas high butyryl content enhances both overall solubility and the formation of liquid-crystalline solutions at lower concentration, it results in lower fiber modulus and strength. Morphology of the fibers depended on the coagulation rate which was influenced by the concentration of the sppinning solution. The level of orientation and crystallinity of the fibers increased somewhat when they were spun from liquid-crystalline solutions. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1105-1114 
    ISSN: 0887-6266
    Keywords: mechanosorptive creep ; ionic interactions ; environmental effects ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose acetate butyrate (CAB) fibers were prepared by spinning from liquid crystalline (LC) solutions containing lithium chloride (LiCl). Ionic interactions were observed between carbonyl oxygen and lithium cation by 13C nuclear magnetic resonance (NMR) spectroscopy. Isotropization of the anisotropic phase by LiCl was found to cause a dramatic rise in the viscosity of LC solutions. The mechanosorptive creep behavior described earlier decreased in the presence of residual LiCl salt, possibly due to the formation of electrostatic interactions between Li+ and CAB backbone. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 201-201 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2045-2054 
    ISSN: 0887-6266
    Keywords: cellulose derivatives ; thermal analysis ; butyric acid ; hexanoic acid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose derivatives with low degrees of substitution (i.e., DS 〈 1.5) often fail to reveal glass transition temperatures (Tg) by virtue of their tenacious adherence to moisture, thus preventing systematic analysis of substituent effects (size and DS) on Tg and Tm transitions. On the other hand, cellulose triesters have Tms that decline with acyl substituent size except when the substituent size becomes very large (i.e., 〉 C6), and they have Tgs within 5-20°C of their Tms. This proximity is unusual for a semicrystalline material, and it interferes with the crystallization process that occurs between Tm and Tg. Triesters of cellulose with mixed acyl substituents (one smaller and one larger) allow not only unambiguous observation of Tgs and Tms but also an adjustable Δ(Tm - Tg) window that depends upon the size and the DS of the larger substituent. The materials studied including cellulose acetate butyrate triesters (DSbu 0.8-2.6), cellulose acetate hexanoate triesters (DShex 0-3.0), and cellulose acetate (DSac 2.44), revealed that only the mixed esters, in which the bulkier acyl group is in the range of DS 0.3-1.0, had a Δ(Tm - Tg) value in excess of 40°C. Although the Tm of cellulose acetate hexanoate declined by ca. 150°C per unit of DShex as DShex rose from 0 to 1, this was only ca. 25°C between DShex of 1 and 3. Frequently observed dual-melt endotherms were attributed to two separate crystal morphologies. ©1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1613-1620 
    ISSN: 0887-6266
    Keywords: cellulose ester ; cellulose esterification ; cellulose acylation ; thermal analysis ; melting point ; glass transition ; side-chain crystallinity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose esters with linear aliphatic acyl substituents ranging in size from C12 (lauric acid) to C20 (eicosanoic acid) were prepared in homogeneous solution (DMAc/LiCl) using a novel synthetic method based on the use of a mixed p-toluenesulfonic/carboxylic acid anhydride. The resulting waxy cellulose esters had a high degree of substitution (DS), between 2.8 and 2.9, and showed little degradation. Thermal analysis of these cellulose derivatives by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) revealed a series of transitions that represented motion by both ester substituents and cellulosic main chain. Broad crystallization and melting transitions attributed to side-chain crystallinity were observed in the range between -19 and +55°C; these side-chain Tm and Tc transition temperatures increased by 10°C per carbon atom of the ester substituent. The Tg of these derivatives increased linearly with increasing substituent size from 94°C for C12 (cellulose laurate) to 134°C for C20 (cellulose eicosanoate). Evidence of “main-chain” crystallization was not observed for these samples, except in the case of peracetylated C12 and C14 esters, which had Tm values of 96°C and 107°C, respectively. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 683-699 
    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 and a cellulose hexanoate ester (DS 0.69) exhibited liquid crystalline behavior in dimethylacetamide/lithium chloride and dimethylacetamide, respectively. The experimentally observed critical volume fraction (Vcp) of cellulose was lower than that predicted by Flory's theory, whereas the experimental and theoretical values of Vcp were within 70% of prediction for cellulose hexanoate. The Vcp value obtained for cellulose hexanoate was lower than that previously reported for cellulose acetate butyrate with a maximum degree of butyration (CAB-3). This indicates that bulky substituents may lower Vcp values. Fibers were spun from isotropic and anisotropic solutions of cellulose and cellulose hexanoate by a dry jet/wet spinning method. There was an increase in mechanical properties through the isotropic to anisotropic transition with moduli reaching 152 g/d (20.8 GPa) for cellulose fibers. The formation of cellulose fibers with high modulus at large extrusion rates and large takeup speeds (draw ratio) is explained with molecular organization prior to coagulation. This unexpected enhancement is attributed to the air gap that exists in the dry jet/wet spinning process. Similar improvements were not observed for cellulose hexanoate fibers. This is explained with incomplete development of liquid crystalline structure at the solution concentrations from which the fibers were spun. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1671-1678 
    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: Tri-O-α-naphthylmethyl cellulose was prepared by homogeneous phase reaction using SO2-diethylamine (DEA)-dimethyl sulfoxide (DMSO) as the solvent system. Observations made by dynamic mechanical spectrometry and by cross-polarized optical microscopy revealed liquid crystalline behavior for the concentrated solutions of tri-O-α-naphthylmethyl cellulose in dimethylacetamide (DMAc). Experimental and calculated (predicted) critical volume fraction of the derivative, Vcp, did not show agreement. It is determined that Vcp is affected by bulky substituents on the cellulose backbone to some extent. © 1993 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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