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  • Polymer and Materials Science  (29)
  • Surface physics, nanoscale physics, low-dimensional systems  (10)
  • Superfluidity and superconductivity  (8)
  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1219-1227 
    ISSN: 0887-624X
    Schlagwort(e): 1,2,4-benzenetricarboxylic acid monoesters ; poly(amide-imide) structural regularity ; poly(amide-imide) “one-pot” synthesis ; 13C-NMR spectra of poly(amide-imide) ; phosphorylation reaction ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aromatic processable poly(amide-imide)s have been prepared according to the Yamazaki and Higashi phosphorylation reaction from flexible aromatic diamines and a mixture of isomeric 1,2,4-benzenetricarboxylic acid monoethylesters following a novel “one-pot” procedure. The polymerization was performed in 1-methyl-2-pyrrolidone/LiCl solutions using triphenylphosphite and pyridine as condensing agents to form amide bonds. Cyclization of the intermediate poly(amide-amic ethylester) occurred by eliminating ethanol under the polymerization conditions used, thus leading to the formation of imide rings. The influence of several parameters which regulate the degree of polymerization and the formation of the imide rings, such as reaction temperature, triphenylphosphite/monomers molar ratio, and pyridine concentration was carefully investigated. In particular, the catalytic activity of pyridine in the imidization reaction has been demonstrated. 13C-NMR spectroscopy has been used to show the absence of constitutional regularity in the prepared PAIs thus indicating equal reactivity toward polycondensation of the two different carboxyl groups of the 1,2,4-benzenetricarboxylic acid monoethylesters. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 385-392 
    ISSN: 1042-7147
    Schlagwort(e): polyamides ; poly(etheramide)s ; thermal behavior ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Processable, thermally stable aramides were prepared from multi-ring flexible aromatic diamines and diacids by direct polycondensation at 100°C with the triphenylphosphitel pyridine system in N-methyl-2-pyrrolidone/LiCl. The monomers used are characterized by the presence of all m-, all p-, or m, p-oriented aryloxy groups and, in some cases, by ring substitution with methyl or phenyl groups. The poly(etheramide)s (PEAs) prepared have moderate polymerization degrees (ηinh 0.55-2.74) and their solubility in organic solvents depends on their structural features. Differential scanning calorimetry (DSC), and wide-angle X-ray diffraction analysis revealed a partial crystallinity for “as-polymerized” PEAs derived from p-oriented monomers. The thermal behavior was investigated by DSC, dynamic-mechanical thermal analysis (DMTA) and thermogravimetric analysis (TGA). The glass transition temperatures, as determined by DSC and DMTA, are spread over a wide temperature range, 140-274°C, and depend on the number of aryloxy groups and their catenation as well as on the presence of ring substituents. The TGA results indicate thermal stability (10% weight loss) up to 490°C. Tough, flexible films are produced by solution casting or by compression molding in the case of amorphous PEAs.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 55 (1995), S. 233-246 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The crystallization kinetics of a polyetheretherketone (PEEK)/liquid crystalline polymer (LCP) blend was studied by using differential scanning calorimetry. Nonisothermal runnings were performed on heating and on cooling at different rates. Isothermal crystallization experiments at 315, 312, 310, and 307°C, from the melt state (380°C) were performed in order to calculate the Avrami parameters n and k and the fold surface free energy, σe. Polarized light optical micrographs were also obtained to confirm the Avrami predictions. It was observed that the LCP retarded the PEEK crystallization process and that the PEEK melting temperature decreased with the amount of LCP, but the LCP melting temperature increased with the amount of PEEK. Probably the PEEK improves the perfection of the LCP crystalline domains. A spherulitic morphology in pure PEEK and its blends was predicted by the Avrami analysis; however this morphology was only observed for pure PEEK and for the 80/20 composition. The other compositions presented a droplet and fibrillar-like morphology. The overall crystallization rate was observed to decrease with the crystallization temperature for all compositions. Finally, σe was found to decrease with the increase of LCP in the blends, having unrealistic negative values. Thus, calculations were made assuming σe constant at all compositions. It was observed that δ, the interfacial lateral free energy, decreased but still remained positive. It was concluded that in these blends neither σe nor σ could be considered constant. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 1813-1820 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Random multiblock polyesteramides (PEAs) having polyester (PE) content of 20-50 wt % have been prepared by low-temperature polycondensation using sebacoyl chloride, 1,6-diaminohexane, and telechelic oligomers of L-lactide with Mn = 600-1500. The PEAs were characterized by IR and 1H-NMR spectroscopy, wide-angle X-ray diffraction, and thermal analysis. Only the polyamide segments are able to crystallize, and the crystallinity depends on the composition and architecture of the PEAs. From viscosity and IR measurements it was established that the chain degradation of PEA powders or films suspended in buffer solutions occurs by hydrolysis of the ester linkages. The degradation rate is influenced by pH, PE content, and, to a lesser extent, by crystallinity. © 1992 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1809-1822 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Random polyesteramides with different chemical compositions and block polyesteramides have been prepared by a two-step polycondensation method from adipolyl dichloride, 1,10-decandiol, and 1,6-diaminohexane. A sample of alternating microstructure has been synthesized by melt polycondensation of 1,10-decandiol and preformed bisesteramides. The thermal and viscoelastic behavior has been investigated and related to the chemical composition and chain microstructure. The random copolymers exhibit one transition in the crystalline phase, whereas two transitions are shown by the block copolymers. The viscoelastic behavior suggests that in the amorphous component a partial microsegregation of phase occurs, generating an intermediate structure between a monophasic and a biphasic amorphous system.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 156 (1972), S. 321-324 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 62 (1977), S. 85-90 
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Die Reaktivität verschiedener monomerer Vinylketone bei der radikalischen Copolymerisation mit Methylmethacrylat und Vinylacetat wurden auf der Basis der Taft-Gleichung untersucht. Es ergab sich, daß die relative Reaktivität der Vinylketonmonomeren mit zunehmender Elektronegativität der Substituenten der verschiedenen Vinylketone steigt. Polare und sterische Effekte beeinflussen die Reaktivität nicht.
    Notizen: The reactivity of some monomer vinyl ketones in the radical copolymerization with methyl methacrylate and vinyl acetate was studied on the basis of the Taft equation. It was concluded that the relative reactivities of the vinyl ketones in radical reactions increase with increasing electron-withdrawing nature of the vinyl ketone substituent. Polar and steric effects do not affect the reactivity.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 181 (1980), S. 1339-1348 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Copolyesters derived from adipic acid, trans-3-hexenedioic acid and 1,16-hexadecanediol were prepared and investigated by means of X-ray diffraction and DSC techniques. From the X-ray results an isomorphous replacement of the saturated and unsaturated diacid units has been suggested. The equilibrium melting temperature Tm0 and the heat of fusion ΔHf were slightly dependent on the copolyester composition. The crystallization process was analyzed by means of Hoffman's kinetic crystallization theory for a lamellar type crystal growth. The values of the free energy of formation of a nucleus of critical dimensions φ* and the free energy of folding σe were found to decrease regularly with increasing amount of double bonds, varying from 110 to 83 kJ/mol for Δφ* and from 171 to 127 erg/cm2 for σe. This effect has been interpreted on the basis of an increase of chain flexibility owing to the presence of the trans double bonds.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamic mechanical behaviour of polyamide systems containing different degrees of unsaturation was analyzed. The results do not show any simple relation between unsaturation and mechanical response. Particular attention was given to the α-transition, that is a glass transition, and experimental data suggest that the generally accepted mechanism for this transition requires a more extensive study.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In order to elucidate the relations between morphological habits, thermal behaviour and chemical structure of polymers, aliphatic polyesters with variable amount of trans-double bonds along the backbone chain were crystallized from dilute solutions in 1-propanol and 1-butanol. The crystals were studied with electron microscopy, differential scanning calorimetry, and wide angle X-ray diffraction. The morphology of solution grown single crystals and some thermodynamic quantities such as the equilibrium dissolution and melting temperature and the enthalpy and entropy of fusion are influenced by the percentage of unsaturated comonomer. The thermal behaviour and the X-ray diffraction of these crystals suggest that saturated and unsaturated repeating units are able to cocrystallize.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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