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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 727 (1983), S. 273-284 
    ISSN: 0005-2736
    Keywords: (Liposome preparation) ; Dimyristoylphosphatidylcholine ; Protein-lipid interaction ; Thermodynamics ; α-Lactalbumin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 205 (1993), S. 140-144 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Thermochimica Acta 238 (1994), S. 1-16 
    ISSN: 0040-6031
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 77-85 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The temperature-concentration diagram for the system atactic polystyrene/trans-decalinSystem. name: trans-decahydronaphthalene. was studied by optical observations and calorimetric investigations. A liquid-liquid demixing interferes with the glass transition of the polymer-solvent system. It results in the solidification of the solution. The binodal, the spinodal and the position of the critical point were investigated for a sample with narrow molecular weight distribution. The formation of different morphologies, based on different cooling processes, is illustrated.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1466-1470 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 fluorescence technique is used to study the mechanism and dynamics of thermoreversible gel formation in concentrated polymer solutions. Two examples of these ordered structures were studied: isotactic polystyrene (iPS) in decalin and syndiotactic poly(methyl methacrylate) (sPMMA) in toluene. iPS can form two types of gels in decalin solutions. Turbid suspensions are formed between 60°C and 130°C. When the solution is quenched beneath 20°C, transparent gels are formed. In the former solution the polymer has a 31 helix structure; in the latter a 121 helix is formed. These structures formed by iPS in decalin solution have different fluorescence spectra. The ratio (Im/Ie) of the intensity of the monomer fluorescence band in the spectrum over the intensity of the excimer emission band is higher in the spectra of transparent gels. The formation of the transparent gels from a solution can be followed by plotting Im/Ie as a function of temperature. The kinetics of the gel formation are studied by following Im/Ie as a function of time at a fixed temperature. sPMMA forms gels in toluene by a mechanism called “conformational gelation.” This mechanism consists of two steps: a fast conformational change followed by a slower aggregation of polymer chains. Both steps were followed by measuring fluorescence of a pyrene label attached to the polymer. The fluorescence lifetime of this probe is sensitive to the polarity of the environment. When the polymer conformation goes from a random coil to an all trans conformation, the environment of the fluorescent label becomes increasingly richer in solvent. This change in polarity is reflected in a change in fluorescence lifetime. The change in fluorescence anisotropy of the label reflects the second step of the mechanism and correlates with the occurrence of chain aggregation.
    Additional Material: 4 Ill.
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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. 241-247 
    ISSN: 0887-6266
    Keywords: thermoreverible gelation ; cooperative interactions ; PVC ; liquid-liquid demixing ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermo reversible gelation of poly(vinylchloride) (PVC) is investigated by calorimetric and optical measurements. In a dynamic heating or cooling scan different thermal transitions are observed. The temperatures of these enthalpic transitions as well as the gel-sol temperatures are dependent upon the fraction of PVC present in the sample and on the solvent quality. After isothermal annealing, supplementary endotherms, formed at a slow rate, are found on heating. The temperature of these isothermally formed endotherms is nearly concentration independent. In a previous paper a model for the gelation of PVC was proposed, based on the formation of cooperative, intermolecular associations possible between subsequent, syndiotactic monomeric units. In this paper it is shown that this gelation mechanism is general and occurs in different solvents. © 1996 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2307-2309 
    ISSN: 0887-6266
    Keywords: polymer solutions ; demixing ; miscibility windows ; Flory-Huggins-Staverman treatment ; acetone/polystyrene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 609-617 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase behavior of poly (vinyl alcohol) dissolved in ethylene glycol and propylene glycol was studied. On cooling a solution in the low concentration range, solidification results from a combination of a liquid-liquid demixing and a crystallization or liquid-solid demixing. This conclusion is based on the results obtained from optical and calorimetric observations and is further supported by the influence of the molecular weight and the solvent quality. It also explains the melting point-crystallization relationship observed after isothermal crystallization of the polymer in presence of the solvent. The mechanism proposed for the thermoreversible gelation of these solution is confirmed.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1891-1900 
    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 thermal behavior in argon of homogeneously synthesized cellulose p-toluenesulfonates (tosylates) with a degree of substitution (DS) ranging from 0.4 to 2.3 was studied by means of thermogravimetry and derivative thermogravimetry from ambient temperature up to 500°C. For comparison, the thermal behavior of the starting celluloses used (pulps, linters, bacterial cellulose) was also examined. The thermal degradation of cellulose tosylates was initiated at lower temperature than cellulose itself and proceeds in two main stages. The temperature of the first one (169 196°C) increases with increasing DS and is independent of the molecular weight. Activation energies calculated following the method of Broido, FTIR, and ultimate analysis as well as mass spectroscopy show that the first stage of degradation is closely associated not only with the scission of tosyl ester groups but also with a partially degradation of the polymer backbone. Further, the temperature-concen-tration diagram for the system cellulose tosylate 20/o-dichlorobenzene was studied by optical observations and calorimetric investigations. A liquid-liquid demixing interferes with the glass transition of the cellulose tosylate-solvent system. It results in the solidification of the solution. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1127-1135 
    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 preparation of porous fibers from the quasi-ternary system poly(methyl methacrylate)/poly(ethyl methacrylate)-1-butanol is based on the combination of different liquid-liquid demixing processes that interfere with the vitrification process. Polymer-polymer demixing takes place at high temperature and interferes at lower temperature with polymer-solvent demixing and the vitrification of some of the formed phases. When these processes take place during extrusion, porous “composite” fibers are obtained. They consist of fibrils of poly(methyl methacrylate) coated with poly(ethyl methacrylate), and these fibrils are separated by micrometer-sized channels that extend along the fiber axis. The formation of these fibers is discussed within the framework of the phase behavior of the quasi-ternary system. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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