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  • Polymer and Materials Science  (30)
  • 2025-2025
  • 1980-1984  (15)
  • 1975-1979  (15)
  • 1
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The influence of weathering and storage in water on the fracture behaviour of glass fibre reinforced polycarbonates was investigated. It was shown, that the stability of adhesion between polymer matrix and glass fibres can be characterized by a multichannel analysis of accoustic emission during a bending test. The interpretation is based on comparisons between accousting emission data, stress-deformations curves and results of scanning electron microscopy.From the dependence of the accoustic emission data and the viscosity ratios on the time of weathering and water storage follows, that the initial decrease of impact resistance an is caused mainly by embrittlement of the polycarbonate matrix. After prolonged exposition to moisture the reduced interfacial bond strength contributes to decreasing impact resistance and flexural modulus.
    Notes: An glasfaserverstakten Polycarbonaten wurde der EinfluR einer Klima- und Was-serlagerung auf das Bruchverhalten untersucht. Dabei wurde nachgewiesen, daf3 sich durch eine Vielkanalanalyse der wahrend eines langsamen Biegeversuchs registrierten Schallemission die Festigkeit der Verbundhaftung zwischen Glasfasern und Polycar-bonatmatrix charakterisieren 1Mt. Die Interpretation stiitzt sich auf einen Vergleich der gemessenen Schallemission mit dem Verlauf der Kraft-Verformungs-Kurven und rasterelektronenmikroskopischen Aufnahmen sowie auf den EinfluB einer Glasfaser-beschlichtung auf die experimentellen Befunde.Aus der Abhangigkeit der Schallemissionswerte und der LOsungsviskositat von der Dauer der Klima- bzw. Wasserlagerung folgt, daR der anfangliche Abfall der Schlag-zahigkeit a,, ubenviegend durch eine Versprodung der Polycarbonatmatrix verursacht wird. Bei langer anhaltender Feuchteeinwirkung tragt dann auch die Lockerung der Verbundhaftung zur Abnahme der Schlagzahigkeit und der Biegefestigkeit bei.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 74 (1978), S. 187-202 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Molecular motions in nylon 6 are studied by thermally stimulated discharge (TSD) techniques. The effect of absorbed water on the relaxation behaviour of nylon 6 is discussed. The γ relaxation process at -145°C is attributed to local segmental motions in the amorphous phase. The intensity of the γ relaxation is reduced and broadened by absorbed water. The molecular origin of the β relaxation process in the temperature range between -80 and -60°C is associated with localized reorientational motions of chain segments involving nonchain-bonded or weakly bonded amide groups. It is quite likely that also rotational rate processes of water molecules bonded to CO-groups contribute to the β process. The intensity increases are due to added water, since associated water molecules are involved with those molecular motions. The α relaxation process at 70°C is associated with large-scale segmental motions at the glass transition. The chain mobility is increased by added water and gives rise to an α peak near 50°C. The α′ relaxation process in the temperature range between 100 and 110°C may either be associated with reorientational motion of stretched chain segments or with the beginning of a crystalline transformation of the γ phase into the monoclinic α form. The temperatures of TSD-peaks correspond to alternating current loss data at a frequency of 5·10-2 Hz.
    Notes: Molekulare Beweglichkeiten in Polyamid-6 wurden mittels der Methode der thermisch stimulierten Entladeströme (TSD) untersucht. Es wurde der Einfluß von Wasser auf die Relaxationsgebiete studiert. Das γ-Dispersionsgebiet mit dem Schwerpunkt um -145°C ist Kettensegmentbewegungen im Amorphen zuzuordnen. Nach Wasseraufnahme wird eine Intensitätsabnahme und Verbreiterung des ß-Dispersionsgebietes beobachtet. Der molekulare Ursprung des sich im Temperaturbereich von -80 bis -60°C ausbreitenden β-Prozesses wird mit lokalen Reorientierungen von CH2-Segmenten verknüpft, die nicht oder nur schwach gebundene Amidgruppen enthalten. Darüber hinaus können Rotationsplatzwechsel an CO-Gruppen gebundener Wassermoleküle zum β-Prozeß beitragen. Nach Wasseraufnahme steigt die Intensität des β-Maximums, da an den Bewegungen dieser Kettenbausteine assoziierte Wassermoleküle teilnehmen. Das α-Dispersionsgebiet bei etwa +70°C stellt den Glasübergang dar, der nach Wasseraufnahme infolge erhöhter Kettensegmentbeweglichkeit schon bei +50°C beobachtet wird. Der α′-Relaxationsprozeß bei 100-110°C kann mit Molekülbewegungen verspannter Kettensegmente oder mit einer beginnenden Kristallumwandlung der γ-Struktur in die monokline α-Form in Verbindung gebracht werden. Die Temperaturen der TSD-Maxima entsprechen Wechselstrom-Verlustdaten einer Frequenz von 5. 10-2 Hz.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 86 (1980), S. 215-224 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: A new method for the simultaneous study of electrical and thermal properties of polymers is proposed. The thermal electrical analysis (TEA) combines the existing techniques of DSC (or DTA) with the electrical method of thermally stimulated discharge (TSD). TEA measurements were carried out with copolymers of methyl methacrylate (PMMA). The molecular origin of the TSD-current at the lower temperature side of the α1-relaxation process (glass transition Tg of the PMMA) is related to the disorientation of small polar segments of the comonomer (α2-relaxation) in the main chain of the PMMA. It can be shown that the TSD-current of the α2-relaxation (T 〉 80°C) increases with increasing comonomer content. This supports the molecular interpretation of the α2-process which is not reflected in the DSC. At higher temperatures frozen in dipoles regain their mobility and show a TSD peak at that temperature which corresponds to the Tg of the PMMA. The TSD ρ-peak at T〉Tg can be attributed to trapped space charges which regain their freedom of motion. The results demonstrate the high resolution and resolving power of the TEA-method. TEA is recommended as an analyzing tool to investigate the relationship between the depolarization of dipoles, carrier transport, trapping of real charges and thermal transitions of polymers.
    Notes: Es wird eine neue Untersuchungsmethode für die gleichzeitige Beobachtung elektrischer und thermischer Eigenschaften von Polymeren dargestellt. Die thermoelektrische Analyse (TEA) verknüpft die bestehenden Techniken der DSC (oder DTA) mit der elektrischen Methode der thermisch stimulierten Entladung (TSD). TEA-Untersuchungen wurden an Copolymeren von Methylmethacrylat (PMMA) oberhalb von Raumtemperatur durchgeführt. Während im DSC-Signal unterhalb der Glastemperatur Tg des PMMA keine Veränderung zu beobachten ist, erkennt man im TSD-Strom bei etwa 80°C das Aufterten einer Schulter (α2-Relaxationsprozeß) auf der Tieftemperaturseite des α1-Maximums (Tg). Da der TSD-Strom linear mit dem Comonomergehalt im Bereich des α2 Relaxationsprozesses ansteigt, wird dieser der Desorientierung von kleinen, polaren Segmenten des Comonomeren in der Hauptkette des PMMA zugeschrieben. Das TSD ρ-Maximum bei T〉Tg kann auf in Haftstellen eingefangene Ladungsträger zurückgeführt werden. Die Ergebnisse lassen erkennen, daß die TEA-Technik eine hohe Empfindlichkeit und Auflösung besitzt und durch ihre gleichzeitige Zuordnung thermischer und elektrischer Größen zu einer Vertiefung der Kenntnisse des elektrischen Leitungsmechanismus und zum Erkennen und Deuten von Relaxationserscheinungen in Hochpolymeren beiträgt.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 5 (1984), S. 57-62 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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  • 5
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyacetylene, (CH)x, has been doped with trimethyloxonium hexachloroantimonate, (CH3)3O+SbCl6-(1), in dichloromethane and acetonitrile. The maximally doped (CH)x films have moderate conductivities [σRT(CH2Cl2) = 10, σRT(CH3CN) = 0.7 Ω-1 cm-1]. Reactions between 1 and (CH)x CH2Cl2 or CH3CN were followed in situ by 1H nuclear magnetic resonance spectroscopy and x-band electron spin resonance spectroscopy. It was found that the reactions in the two solvents are different. In dichloromethane the dopant is SbCl5, which forms from the decomposition of 1, and doping proceeds by electron removal from (CH)x chains. Based on the ESR signal loss, an estimate can be made of the diffusion rate of SbCl5, into the (CH)x fibrils in CH2Cl2; it is found to be ca. 10-17 cm2/s. In acetonitrile the dopant appears to be either CH3CNCH3+, H+, CH3+, or a combination of one or more of these dopants. It is postulated that the CH3CNCH3+, CH+3, and/or H+ dopant covalently binds to the (CH)x chain. X-ray photoelectron spectra show that films doped with excess 1 in both solvents have approximately one SbCl6- per 33 CH units.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 34 (1983), S. 764-764 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0009-286X
    Keywords: betriebsbeanspruchte Bauteile ; Stahl 13 CrMo 44 ; Zeitstandbeanspruchung ; Gefügebeurteilung ; mechanische Eigenschaften ; Zeitstandverhalten ; weitere Verwendbarkeit ; Restlebensdauer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 49 (1977), S. 339-340 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 56 (1984), S. 356-360 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Energy savings in industrial NH3 plant by heat recovery in the waste heat system. Minimization of energy consumption is nowadays a primary goal in the design of NH3 plant. In this context two aspects are particularly important: first, the process steps and their combination must be selected in such a way that the level of energy that has to be supplied to the plant is kept low from the very beginning; second, heat recovery must be optimized by the choice of process conditions and use of appropriate equipment. An industrial NH3 plant built according to these principles can operate at a consumption of as low as 29.5 GJ/t NH3, using proven processes and equipment. The first plant of this new generation with a capacity of 1120 t/d is currently under construction for Canadian Industries Ltd. (CIL) in Canada.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 56 (1984), S. 806-806 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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