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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1643-1651 
    ISSN: 0887-6266
    Keywords: polyoxadiazoles ; structural analysis ; cristallinity behavior ; cyclodehydration reaction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new series of poly(ether-alkyl)oxadiazoles of general formula: with m = 3, 4, and 5 has been obtained from the corresponding polyhydrazides through thermal cyclization reaction. The polymers were characterized by infrared spectroscopy, differential scanning calorimetry, wide-angle x-ray analysis, and optical microscopy. The polymers were crystalline, with a crystalline texture and structural parameters strongly dependent on the value of m. The Tm's and Tg's value decreased with increasing number of CH2. © 1994 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0887-6266
    Keywords: polyoxadiazoles ; IR ; structure ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly-ether-aroyl-oxadiazoles (PEODZ) of general formula: are reported.Thermal cyclization of the starting polyhydrazides, infrared, thermal, and structural characterization are discussed as function of the number of methylene spacers in the range 2-12.It is found that the position of melting is strongly dependent upon the number of—CH2—, and that moldable polyoxadiazoles are obtained at × values 〉 7. The spherulitic nature of PEODZ is clearly revealed by thermal-optical microscopy which, together with isothermal crystallizations at the differential scanning calorimeter, gives a close insight into the crystalline organization of such polymers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2025-2035 
    ISSN: 0887-6266
    Keywords: high density polyethylene ; hydrogenated oligo (cyclopentadiene) ; miscibility ; blends ; phase structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The article discusses the influence of an oligomeric resin, hydrogenated oligo (cyclopentadiene) (HOCP), on the morphology and properties of its blends with high density polyethylene (HDPE). HDPE/HOCP blends after solidification contain three phases: the crystalline phase of HDPE and two amorphous phases, one rich in amorphous HDPE and the other in HOCP. DSC thermograms and the loss modulus behaviors show that the γ transition is influenced by HOCP molecules and, in addition to the αc transition of HDPE, there is another transition that is attributed to the HOCP-rich phase. The hypothesis of the two amorphous phases is confirmed by the optical microscopy observations performed on isothermally crystallized blend films. © 1994 John Wiley & Sons, Inc.
    Additional Material: 13 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 33 (1995), S. 1723-1730 
    ISSN: 0887-6266
    Keywords: high density polyethylene ; hydrogenated oligo(cyclopentadiene) ; blends ; phase structure ; stress-strain ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of hydrogenated olio(cyclopentadiene) (HOCP) on tensile mechanical properties of its blends with high density polyethylene (HDPE) has been studied at 20, 80, and 100°C. The nominal stress-strain curves performed at 20°C indicate an increase of the modulus and a conspicuous decrease of the ultimate properties increasing the HOCP content in the blend. Blends with HOCP content 〉 20%-wt are found to be very fragile at 20°C. These behaviors have been related to the presence of the HOCP-rich phase that has the glass transition at about 55°C. At 20°C the HOCP oligomers act as a hardener for the HDPE. The nominal stress-strain curves performed at 80 and 100°C show a strong decrease of the modulus (compared to the value at 20°C), plastic deformation for all the blends tested, and rupture of HDPE and blend samples at the beginning of the cold-drawing. Moreover, the modulus and the ultimate parameters are found to decrease with the composition. The behaviors at 80 and 100°C have been related to several factors: the higher mobility of HDPE molecules at these temperatures compared to that at 20°C; the HOCP-rich phase that is at temperatures higher than its glass transition, and so it acts as a plasticizer for the HDPE; and the decreases of crystallinity and number of entanglements when the HOCP is added to the HDPE component. ©1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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