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  • 1985-1989  (9)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 7 (1988), S. 563-566 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 30 (1985), S. 1317-1324 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Das mesophasische Verhalten der folgenden Verbindungen wurde mittels DSC, Röntgendiffraktion und optischer Mikroskopie untersucht: CH3(CH2)4-CO-R-A n -R-CO-(CH2)4-CH3;n=9→14, 16 CH3(CH2)4-CO-R-B n -R-CO-(CH2)4-CH3;n=2, 3A n =-CO-O-(CH2)n-4-O-CO-;B n =-CO-(OCH2CH2)n-O-CO-;R=-O-C6H4-C(CH3)=N-N=(CH3)C-C6H4-O-. Die Verbindungen wurden als Modelle homologer nematogener Polymere mit niedrigem Molekulargewicht angesehen. Alle untersuchten Verbindungen zeigen einen nematischen Mesomorphismus. Analog zu den entsprechenden Polymeren zeigen die sich auf den nematisch-isotropen Phasenübergang beziehenden thermodynamischen Daten eine, wenn überhaupt, sehr reduzierte ungerade-gerade Fluktuation. Diese Daten werden mit denen verglichen, die für sehr ähnliche, sowohl polymère als auch nicht-polymere Verbindungen mit Esterbindungen zwischen den starren und flexiblen Gruppen erhalten wurden, um Beweise für die Zuverlässigkeit der auf dimeren Verbindungen aufbauenden Modelle für polymère Homologe zu erhalten.
    Abstract: Резюме Методами ДСК, рентген офазового анализа и оптической микроско пии исследовано мезофазное поведени е соединений со следу ющей структурой: CH3(CH2)4-CO-R-A n -R-CO-(CH2)4-CH3 n=9→14,16 CH3(CH2)4-CO-R-B n -R-CO-(CH2)4-CH3 n=2, 3A n =-CO-O-(CH2) n−4-O-CO-;B n =-CO-(OCH2CN2) n -O-COR =-O-φ-C(CH3)=N-N=(CH3)C-φ-O- φ=C6H4 Предполагалось, что э ти вещества являются низкомолекулярными модельными соединен иями гомологов жидкокрис таллических полимер ов. Все исследованные соеди нения проявляют жидкокристаллическ ий мезоморфизм. Термодинамические д анные относительно ф азового перехода нематик — из отроп, показывают оче нь пониженную, по аналог ии с соответствующим и полимерами, четную-не четную флуктуацию. Да нные сопоставлены с таков ыми, полученными для подобных полимер ных и не полимерных со единений, содержащих эфирные з венья между жесткими и гибкими гр уппами, для доказател ьства достоверности этих д имерных соединений как моделей полимерн ых гомологов
    Notes: Abstract The mesophasic behaviour of the following compounds has been investigated by DSC, X-ray diffraction and optical microscopy methods: CH3(CH2)4-CO-R-A n -R-CO-(CH2)4-CH3,n=9→ 14, 16 CH3(CH2)4-CO-R-B n -R-CO-(CH2)4-CH3,n=2, 3A n=-CO-O-(CH2)n−4-O-CO-,B n =-CO-(OCH2CH2) n -O-CO-,R=-O-Ø-C(CH3)=N-N=(CH3)C-Ø-O-,Ø=-C6H4 They have been assumed to be low molecular weight models of homologous nematogenic polymers. All the examined compounds exhibit nematic mesomorphism. On complete analogy with the corresponding polymers, the thermodynamic data relative to the nematic-isotropic phase transition show a very reduced, if any, odd-even fluctuation. These data are compared with those obtained for very similar compounds, both polymeric and non-polymeric, containing ester linkages between the rigid and flexible groups, to provide evidence of the reliability of the dimeric compounds as models of the polymeric homologues.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 31 (1986), S. 597-603 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Uniaxial orientierte und unorientierte ataktische Polystyrenproben wurden vor und nach dem Tempern bei 80° mittels DSC untersucht. Mit länger werdender Temperungszeit erscheint in endothermer Peak, dessen Fläche mit der Dauer der Temperungsperiode ansteigt. Die Flächen der endothermen Peaks von orientierten und unorientierten Polymeren unterscheiden sich nicht. Die DSC-Kurve von ungetempertem orientiertem Polystyren zeigt einen exothermen Relaxationseffekt. DSC und Relaxationsuntersuchungen ergaben, daß dieser exotherme Relaxationseffekt unabhängig von der Orientierung der Hauptkette ist und eher einer Probeverdichtung zuzuschreiben ist.
    Abstract: Резюме Проведен ДСК анализ о дноосно ориентирова нных и неориентированных атактических образц ов полистирола до и по сле их отжига при температу ре 80°. При увеличении времени отжига появл яется эндотермическ ий пик, площадь которого уве личивается с увеличением периода отжига. Не наблюдалос ь различий между площадью эндот ермического пика ориентированно го и неориентированн ого образцов полимера. На кривой ДС К ориентированного полистирола, не подве ргнутого отжигу, наблюдается релакса ционная эксзотерма. ДСК и релаксационные исследования показа ли, что релаксационная эксз отерма не зависит от ориентации главной ц епи полимера, а обусло влена скорее уплотнением о бразца.
    Notes: Abstract DSC analysis was performed on uniaxially oriented and unoriented atactic polystyrene samples prior to and after annealing at 80 °C. With increasing annealing times, an endothermic peak appeared, whose area increased with the duration of the annealing period. No difference was found between the endotherm areas for the oriented and the unoriented polymer. The DSC curve of the unannealed oriented polystyrene exhibited a relaxation exotherm. DSC and relaxation studies indicated that this relaxation exotherm was independent of the main chain orientation; it may rather be due to sample densification.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 31 (1986), S. 1375-1375 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    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 24 (1986), S. 1805-1812 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The CO2 solubility in oriented and unoriented atactic polystyrene films has been investigated. Orientation does not change the nature of the sorption process; however, it decreases the level of solubility. Both the Langumir sorption term and the Henry's-law contribution are affected by orientation. The decrease of solubility is correlated with an increase of density due to orientation. A simple experiment has been described to evaluate the depression of the glass transition temperature of polystyrene containing dissolved carbon dioxide.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1334-1337 
    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: The chain orientation, induced by hot drawing, decreases the sorption capacity of polystyrene due to the tighter packing of macromolecules in the oriented material. Density measurements and decay of birefringence indicate that the loss of orientation Is a much more rapid phenomenon than the thermal shrinkage of the polymer.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 1203-1206 
    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: Thermal treatment of amorphous poly(aryl-ether-ether ketone) below the glass transition temperature has been studied. The extent of aging was measured by differential scanning calorimetry. X-ray and Fourier transform infrared spectra were used to study both melt-cast and annealed samples. The effect of the thermal treatment of viscoelastic response was evaluated using creep tests. Aging has been shown to be accompanied by a marked change in the transport properties of the material.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 153-162 
    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: Thermotropic liquid crystal polymers have been modeled as an array of highly ordered polyhedric nematic domains immersed in a less-ordered, nearly isotropic matrix. A function has been defined that expresses the elastic moduli of drawn fibers as a function of orientation and geometry of the nematic domains. When such a material is hot drawn in extension, the domains orient and elongate to produce an orthotropic fibrous phase. Equations are proposed to relate the elastic moduli of the fibers to the draw ratio and the extrusion conditions. Upon annealing of the hot drawn fibers, shrinkage occurs. It is proposed that the shrinkage is the result of a physical transformation from the fibrous state back to the nematic domain structure present before extrusion and drawing. The Avrami equation is used to describe the nucleation and growth processes controlling the shrinkage at constant annealing temperature. The model is shown to correlate experimental data on the elastic properties and the shrinkage of hot drawn PET/PHB60 liquid crystal polymer with the processing conditions.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 244-257 
    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: Blends of polycarbonate (PC) and poly(ethylene terephthalate-co-p-oxybenzoate) (PET/PHB60) were prepared by melt-blending. Physical and/or chemical interactions between the two phases of the system were studied by thermal analysis and infrared spectroscopy. Rheological measurements in shear flow were carried out both in the low and high shear rate regions in the temperature range of the existence of the mesophase. At low liquid crystalline polymer (LCP) content, the blends showed flow curves similar to those of the unfilled PC, while at higher LCP percentages the rheological behavior of the pure LCP was resembled. Moreover, in the whole shear range, the viscosity values of such blends were in between those of the pure polymers. The influence of the addition of 10% LCP on the mechanical properties of the PC was investigated. Fiber-spinning was performed under different experimental conditions, and it was found that opportune drawing conditions are necessary to improve the modulus of the matrix. Morphological analyses of the pure LCP and of the blends were related to the rheological and mechanical behavior of these systems. While the LCP exhibited an elevated dimensional stability, the inclusion of the LCP in PC matrix did not improve the dimensional stability of the blends.
    Additional Material: 25 Ill.
    Type of Medium: Electronic Resource
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