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  • Polymer and Materials Science  (23)
  • Fatigue behavior  (1)
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  • 1
    ISSN: 1572-8935
    Keywords: Fatigue behavior ; C.F./PEEK ; Composites ; Weibull distribution function ; Hygrothermal ; Impact
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The hygrothermal effects on the fatigue behavior of the Carbon/PEEK laminated composites before and after impact damage were examined in this study. The [0/45/90/-45]2s AS-4/PEEK laminated composites were immersed in 80°C hot water for 45, 90 and 200 days,and subjected to falling weight impact with an energy of 8.58 J and then immersed in 80°C hot water for 45 days. It was found that the tensile strength of AS-4/PEEK laminated composites decreased with the increase of exposure period. The injured AS-4/PEEK composites were subjected to a static load and a tensiontension fatigue load at various levels of stress amplitudes. The effect of stress amplitude on the fatigue life was studied. The experimental fatigue life under different stress amplitude tests were estimated by the median rank order statistic cumulative distribution function. Then,the fitting curves for estimated data were analyzed by the Weibull distribution function. The S-N curves for a series of cyclic loads at various survival probabilities were presented. The damage behaviors of composites after fatigue load test were also investigated by scanning electron microscope(SEM). Results indicated the fatigue lives of immersed specimens were shorter than those without hygrothermal effect, the impact damage affects the fatigue life of composite significantly.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 235 (1996), S. 35-45 
    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: Ein Phenolharz-Polyurethan-Copolymeres wurde aus einem Phenolharz, einem geschützten Polyurethan und p-Toluolsulfonsäure hergestellt. Dieses Copolymere weist trotz großer Härte eine gute Verarbeitbarkeit (einschließlich Topfzeit und Reaktivität) auf. Die Synthese des Copolymeren wurde mit IR-Spektroskopie verfolgt. Es wurde gefunden, daß die Isocyanatgruppe des Polyurethans nach Abspaltung der Schutzgruppe mit der Hydroxygruppe des Phenolharzes reagierte. Glasfaserverstärkte Verbundwerkstoffe offenbarten bei SEM-Untersuchungen eine hervorragende Verbindung zwischen Faser und Matrix. Ein Überlappungspeak im DMA-Diagram wies auf Wechselwirkungen zwischen Phenolharz und Polyurethan hin, die die Härte des Phenolharzes verbessern.
    Notes: A phenolic resin/polyurethane copolymer was synthesized by reaction of a phenolic resin, a blocked-polyurethane and p-toluene sulfonic acid. The copolymer provides a good balance between the processability (including pot life, reactivity) and toughness. The reactions that proceeded during the synthesis of the copolymer was investigated by IR spectroscopy. It was found that blocked polyurethane reacted with the hydroxy group of the phenolic resin. Glass fiber-reinforced composites showed excellent bonding between fiber and matrix as revealed by SEM photographs. An overlap peak was found from the DMA diagram; it indicated that an interaction existed between phenolic resin and polyurethane and that improved the toughness of the phenolic resin.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1153-1159 
    ISSN: 0887-624X
    Keywords: hydrophilic ; thermotropic ; liquid crystalline polymers ; block copolyetheresters ; melt polycondensation ; poly (ethylene oxide) segment ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The block copolyetheresters with a hard segment of poly (hexamethylene p,p′-bibenzoate) and a soft segment of poly (ethylene oxide) were prepared by melt polycondensation of dimethyl-p,p′-bibenzoate, 1,6-hexanediol, and polyethylene glycol (PEG) with molecular weights of 400, 1000, 2000, or 4000. These block copolyetheresters were characterized by intrinsic viscosity, GPC, FT-IR, 1H-NMR, and water absorption. The thermotropic liquid crystalline properties were investigated by DSC, polarized microscope, and x-ray diffraction. The block copolyetheresters exhibit smectic liquid crystallinity due to the polyester segment. The transitions are dependent on the molar content and the molecular weight of PEG used. The block copolyetheresters show high water absorption due to the hydrophilic nature of the poly (ethylene oxide) segment. The water absorption increases with increasing PEG content. As the molecular weight of PEG increases, the water absorption increases significantly. The results indicate that the water absorption of the poly (ethylene oxide) segment in the block copolymers is affected by the presence of polyester segments. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3303-3312 
    ISSN: 0887-624X
    Keywords: epoxy ; blend ; polycarbonate ; transesterification ; cyclization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of oxirane with carbonate using quarternary ammonium salts as catalyst has been studied. Curing is caused by the transesterification reaction of the oxirane cycle with the carbonate group that proceeds by an “insertion” mechanism in the stoichiometric system. The ratio of the reactants is two oxirane groups to one carbonate group. In the nonstoichiometric system, the epoxide content is more than the stoichiometric quantity required. A cyclization reaction is followed by the transesterification reaction. To identify the finished products, a model reaction was proposed using diphenyl carbonate and phenyl glycidyl ether which results in the formation of 4-phenoxymethyl-1,3-dioxolane-2-one (PMD). The mechanism of forming the cyclic structure is assumed to proceed through the chain scission of the network in which the molecular chain crosslinked with carbonate group by a transesterification reaction. © 1996 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 220 (1994), S. 133-149 
    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: Die Klebeeigenschaften und das Phasentrennungsverhalten von Polyurethanen aus „weichen“ Poly(oxypropylen)-Einheiten (PPG) und „harten“ Segmenten aus Toluoldiisocyanat (TDI) und 1,4-Butandiol (BD) wurden untersucht. Die Länge der PPG-Weichsegmente (PPG mit MW 700, 1000 bzw. 2000) sowie deren Konzentration (30, 50 and 70 Gew.-%) wurden variiert. Die Isocyanat-Endgruppen dieser PU-Harze wurden mit 2,3-Epoxy-1-propanol zu Glycidyl-Endgruppen umgesetzt. Die Klebeeigenschaften bei der Temperatur flüssigen Stickstoffs folgen dem Phasentrennungsverhalten der Polyurethane. Die Phasentrennung wurde mit DSC-(Enthalpiesprung bei der Glasternperatur) und IR-Messungen (Veränderungen im Bereich der N—H- und C=O- Streckschwingungen) untersucht. Die rnodifizierten PU-Harze weisen neben verbesserter Haftung bei tiefen Temperaturen auch gute Lagerungseigenschaften sowie die Fähigkeit der Härtung bei Raumtemperatur auf.
    Notes: 2,3-Epoxy-1-propanol has been introduced into isocyanate-terminated polyurethane to form glycidyl-terminated polyurethane resins. A series of glycidyl-terminated polyurethanes based on hydroxyterminated poly(oxypropylene) (poly(oxypropylene) glycol, PPG), toluene diisocyanate (TDI), and 1,4-butanediol (BD) was synthesized with various PPG soft segment lengths (MW 700, 1000 and 2000) and soft segment concentrations (30, 50 and 70 wt.-%). The effects of glycidyl-terminated polyurethane on the adhesion properties and the phase separation were investigated. The adhision properties at liquid nitrogen temperature coincide with the phenomenon observed in the phase separation behavior of polyurethane. Differential scanning calorimetry (DSC) and infrared technique (IR) were used to assess the phase separation content. The enthalpy jump at the glass transition temperature (ΔCp) and the unique spectroscopic features in the N—H and C=O stretching regions were applied to characterized the phase separation behavior. It was found that the modified resins do not only show superior adhesion at liquid nitrogen temperature but also exhibit some unique properties, e.g., room temperature curing and good storage stability.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2183-2191 
    ISSN: 0887-6266
    Keywords: epoxy ; blend ; polycarbonate ; transesterification ; transamidation carbamate ; urea ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transamidation reaction converts the carbonate and amine into N-aliphatic aromatic carbamate and urea, causing the equivalent of oxirane and amine nonstoichiometric in the primary cure stage. After postcure, the substitution reaction takes place and results in a more tightly crosslinked structure. Such a higher crosslinking density is responsible for higher Tg, tensile strength, and tensile modulus in the postcure stage than that in the primary and secondary cure stages. This trend is more pronounced in those PC-epoxy blends containing higher molecular weight aliphatic amine or a higher content of PC. This phenomenon is due to the difference in the fraction of amino group of aliphatic amine consumed in the transamidation. PC-epoxy/aliphatic amine blends show minor improvement in the high strain rate Izod impact tests, while toughness improvement for some blends is substantial at low strain rate tensile tests. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2183-2191, 1997
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1721-1729 
    ISSN: 0887-6266
    Keywords: phenolic ; miscibility ; hydrogen bonding ; PEO ; PEG ; PVA ; glass transition temperature ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The specific interaction strength of novolak-type phenolic resin blended with three similar polymers [i.e., poly(ethylene oxide) (PEO), poly(ethylene glycol) (PEG), and poly(vinyl alcohol) (PVA)] were characterized by means of glass transition temperature behavior and Fourier transform infrared (FTIR) spectroscopy. The interassociation formed within phenolic blends with the addition of a modifier not only overcomes the effect of self-association of the phenolic upon blending, but also increases the strength of phenolic blend. The strength of interassociation within the phenolic blend is the function of the hydrogen bonding group of a modifier, in increasing order, is phenolic/PVA, phenolic/PEG, and phenolic/PEO blend, corresponding to the result of “q” value in the Kwei equation. The FTIR result is in agreement with the inference of Tg behavior. In addition, the fact that the specific strength of hydrogen bonding of hydroxyl-hydroxyl is stronger than that of hydroxyl-ether can also be concluded. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1721-1729, 1998
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 46 (1992), S. 949-957 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Unidirectional fiber reinforced blocked polyurethane (PU) composites have been prepared by the pultrusion process. The effects of processing variables on the mechanical properties and dynamic mechanical properties of fiber reinforced PU composites by pultrusion have been studied. The processing variables investigated included pulling rate (in-line speed), die temperature, postcure time and temperature, and filler type and content. The dynamic mechanical properties of the composites produced by the process were studied utilizing dynamic mechanical spectrometer. Results show that the composites possessed various optimum pulling rates at different die temperatures. From the DSC data analysis, swelling ratio, and mechanical properties, the optimum die temperature was determined. It was found that the mechanical properties increase with filler content for various types of filler. The increasing of mechanical properties depends on the optimum postcure temperature and time. However, the properties decreased for longer postcure times since the composite materials were degraded. The glass-transition temperature (Tg) increased slightly and the damping peak (tan δ) was broadened due to fiber reinforcement. The dynamic mechanical moduli (G′, G″) of pultruded PU composites are apparently higher than those of the matrices. The moduli (G′, G″) increase with increasing fiber and filler content, and the damping peak becomes broad. Effect of postcuring on the degree of crosslinking, Tg, and dynamic modulus will be discussed.
    Additional Material: 15 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 759-764 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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 thermokinetic behavior of blocked polyurethane-based composites during the pultrusion of glass-fiber reinforced composites is investigated utilizing a mathematical model accounting for the heat transfer and the heat generation during curing. The equations of continuity and energy balance, coupled with a kinetic expression for the curing system, are solved using a finite difference method to calculate the temperature and conversion profiles in the thickness direction in a rectangular pultrusion die. A kinetic model, dP/ dt = A exp(-E/RT) (1-P)nPm, was proposed to describe the curing behavior of a blocked polyurethane resin. Kinetic parameters for the model were obtained from dynamic differential scanning calorimetry (DSC) scans using a multiple regression technique, which was able to predict the effects of processing variables on the pultrusion. The effects of process variables (e.g., pulling rate, die temperature, and die thickness) on the performance of the pultrusion are also evaluated. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1137-1151 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Glycidol was used to convert the isocyanate-terminated polyurethane prepolymer to glycidyl-terminated polyurethane prepolymer. The modified polyurethane not only offers some distinct advantages over the commercial polyurethane prepolymer, but also enhances the properties of the epoxy resins. The glycidyl-terminated polyurethane modified epoxy resin proved to be superior to conventional epoxy resins in improving impact strength, fracture energy, and adhesion properties. The compatibility of the compounds in this glycidyl-terminated PU/epoxy system was investigated using different preparation procedures. It was found that the synthesized glycidyl-terminated polyurethane prereacted with curing agents, exhibited a lesser degree of phase separation, and can influence the mechanical properties of polymer blends. The results coincide with the phenomena observed in dynamic mechanical analysis and scanning election microscopy. © 1994 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
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