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  • 1990-1994  (16)
  • Polymer and Materials Science  (16)
  • Tetrafluoroethene  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 1129-1138 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The surface tensions (γ) of a branched polyethylene and two side-group liquid-crystalline (lc) polyacrylates were measured in the isotropic, nematic and smectic states by the pendant-drop method. The surface tension vs. Temperature characteristics of the lc polyacrylates studied show anomalous behaviour. The slope in the isotropic state is initially negative but changes its sign near the isotropic-nematic transition. The increase of γ with decreasing temperature is regained in the nematic phase, until at the nematic-smectic transition the surface tension of the lc polymers discontinuously jumps to higher values and shows a very low temperature coefficient. The observed features have been found to be partly in agreement with the results of surface tension measurements on low-molar-mass liquid crystals, which indicates that the surface properties of the lc polymers are governed by the mesogenic side groups.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 1125-1135 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new route of synthesis of liquid-crystalline polymethacrylates was investigated. The synthetic route involved side-group liquid-crystalline polymethacrylates (LCPMA) with a turned ester group between the aromatic rings in the central unit of mesogens (2) as compared with the usual LCPMA (1). For a series of compounds of this type the liquid-crystalline properties were investigated using differential scanning calorimetry, polarizing microscopy and X-ray diffraction techniques. Generally stable smectic phases were found for these isomeric LCPMA. The described synthetic route opens possibilities to form new polymers from a wide field of educts.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 3097-3115 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of the spacer length (n = 2, 6, 8 and 11 methylene groups) on the polymorphism and the ferroelectric properties of liquid crystalline side-group polyacrylates with a 4-[(R)-4-(1-methylheptyloxy)-4′-biphenylyloxycarbonyl]phenoxy moiety was studied. Various molecular weights were obtained from the polymers with n = 8 and n = 11. All the polymers show SmC* phases. A SmC* phase polymorphism was even found for most of the polymers. In some of these SmC* phases, no ferroelectric properties could be measured. The structural differences between the SmC* phases and their influence on the appearance of the ferroelectric properties are not yet clear. However, a SmC̃* phase was put in evidence, revealing a tendency to a chevron-like ordering which may explain the complex SmC* polymorphism of these systems.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 339-351 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization of amorphous poly(phenylene sulfide) was carried out upon annealing in the presence of sorbed CO2 and N2O at pressures of 50 bar. Thermal crystallization at the same pressure allows the comparison of crystallization rates. From the results of IR-spectroscopy, wide angle X-ray diffraction, differential scanning calorimetry and density measurements, it is seen that in the presence of sorbed gas molecules crystallization occurs even at temperatures below the glass transition measured at atmospheric conditions. At a given temperature, gas sorption yields accelerated crystallization. The results, show the considerable plasticizing influence of sorbed gas molecules. From the crystallization rate at sorbed gas conditions the plasticizing ability of the gas may be estimated. That of N2O exceeds that of CO2 by a factor of three. Assuming a simple two-phase model for the crystalline polymer the comparison of heat of melting and density values for t → ∞ allows the conclusion that parts of the noncrystalline volume fraction become less dense by annealing in the presence of sorbed gas molecules. An increased free volume fraction which may be formed in the non-crystalline regions is discussed. It is possible that the remaining lower density results from a hindered relaxation of chain molecules from the dilated state they take due to gas sorption. In this context the influence of decreased mobility of non-crystalline chains is discussed in terms of the “rigid amorphous phase” concept.
    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 193 (1992), S. 3031-3035 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase separation behavior of graft copolymers containing poly(methyl methacrylate) grafts attached to a side-chain liquid-crystalline backbone is described and examined with respect to the share and the length of the grafts. Only copolymers with a low PMMA content show microphase separation. An increasing PMMA content leads to a miscibility of the components.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 431-444 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption behaviour of CO2 and N2 in poly(p-phenylene sulfide), PPS, crystallized in the presence of CO2 and N2O molecules was studied at 298 K in the pressure range of 1-30 bar. The CO2 transport properties of these samples were investigated at the same temperature in the pressure range of 1-20 bar. The temperature dependence of the CO2 transport parameters was examined between 293 and 343 K at a pressure of 5 bar, for the virgin material, thermal and CO2 crystallized specimen only. All measured properties are compared with those of PPS crystallized by annealing at vacuum conditions to a similar degree of crystallinity, and with the virgin, nearly amorphous material. For the samples crystallized in the presence of sorbed gases an increased CO2-solubility was observed. A part of unrelaxed free volume is proposed to remain in the samples after crystallization in presence of sorbed gas molecules. These voids formed under sorbed gas conditions seem to be stable even after removal of the sorbed molecules. The measured diffusion coefficients for CO2 were lower in the samples crystallized in the presence of gas molecules, compared to the virgin sample. This is expected to be due to an increased diffusive resistance by passing the interfaces of the formed voids. Permeability, which is governed by both, diffusion and sorption, undergoes non-uniform changes. An attempt is made to explain this behaviour based on the dual-mode-sorption and dual-mobility model.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric spectroscopy in the microwave regime (106-1010 Hz) is employed to study the molecular dynamics of a set of ferroelectric liquid-crystalline side group polymers with variable spacer length and different molecular weight, and on their low-molecular-weight counter-part. One relaxation process is observed, the β-relaxation, which is assigned to the hindered rotation of the mesogens around their long molecular axis. This librational process is nearly uninfluenced by the molecular weight and depends only slightly on the spacer length. At the smectic-smectic phase transition SA/SC* the β-relaxation does not decrease in its relaxation strength and shows no slowing down of its relaxation rate. This is in pronounced contrast to the common explanation of the origin of ferroelectricity in liquid crystals and requires a new interpretation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 2047-2061 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilute and semidilute solutions of fractions of a liquid-crystalline side-group polymer were investigated by means of size-exclusion chromatography (SEC), static light scattering (LS), density and viscosity measurements. The mass-average molar mass ranged from M̄w = 1 · 105 g · mol-1 to 1,5 · 106 g · mol-1. Large discrepancies were found between the molar mass determined through SEC and through LS. Strong interactions between the mesogenic groups can be assumed by the results of density and LS measurements. Due to the determined characteristic ratio of C∞ = 19,5 a similar chain stiffness as a poly(alkyl methacrylate) of equal length of the side chain is observed. In semidilute solutions an excess low-angle scattering (ExLAS) occurs which increases at higher concentrations. The dependence of the reduced osmotic modulus [M̄w/(RT)](∂π/∂c)T on the parameter x = A2 · M̄W · c was studied.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structural properties of side-group liquid-crystalline polymers with large electronegative space-filling substituents at the mesogenic groups were investigated. The synthesis and characterization of some poly[m-bromo-p-(methacryloyloxyalkyleneoxy)benzoate]s are reported. Their liquid-crystalline properties were investigated using differential scanning calorimetry and X-ray diffraction techniques and were compared to some unsubstituted compounds found in the literature. A general decrease in the phase transition temperatures and in the order of the liquid-crystalline phases for the Br-substituted compounds was observed. It can be concluded that the liquid-crystalline properties of polymers with large side-group substituents at the mesogens can be maintained if long flexible or large electron-rich end groups are introduced.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 329-333 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This paper reports on the synthesis and characterization of graft copolymers built up by amorphous poly(methyl methacrylate) grafts and a side-chain liquid-crystalline backbone. The interest was focussed on the copolymerization behaviour of the liquid-crystalline monomers and styryl-terminated methyl methacrylate macromonomers. The radical polymerization of the liquid-crystalline monomers depends on the liquid-crystalline monomer concentration and on the amount and length of the grafts (macromonomers). The liquid-crystalline backbone is the longer the higher the concentration of the mesogenic monomers itself and the smaller the molecular weight of the macromonomers. Variation of the amounts of grafts yielded a maximum length of the liquid-crystalline backbone at approximately 4 mol-% (for a molecular weight of 7800 of the graft).
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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