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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 1 (1994), S. 197-203 
    ISSN: 1572-8935
    Keywords: Polymer blend ; Polycarbonate ; PET ; Rubber-toughening ductile-brittle transition temperature
    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 intrinsically impact brittle nature of the PC/PET blends can be effectively toughened by incorporating butylacrylate core-shell rubber. The rubber-modified PC/PET blend possess both excellent low temperature impact properties and reduced notch sensitivity. The ductile-brittle transition temperature of the blend decreases with the increase of rubber content. The presence of rubber in the PC/PET blend does not relieve the strain rate induced yield stress increase. Two separate modes, localized shear yielding and mass hear yielding, work simultaneously in the rubber toughening mechanism. The plane-strain localized shear yielding dominates the toughening mechanism at lower temperature and results in brittle failure. At higher temperature, the planestress mass shear yielding dominates the toughening mechanism and results in ductile failure. The critical plastic zone volume can be used to interpret the observed phenomenon.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8935
    Keywords: Epoxy ; Blend ; Polycarbonate ; Transesterification
    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 PC-DER331 blends are transparent and homogeneous due to the transesterification taking place during hot melting process. This transesterification reaction does not occur or occurs insignificantly during the preparation of PC-DER332 blends. PC is separated from the PC-DER332 melt mixture by slow cooling to room temperature but the mixture remains a single phase by quenching with an ice bath. Two systems of PC-epoxy blends, PC-DER331 blends and PC-DER332 blends are cured by the m-phenylene diamine (MPDA) in a stoichiometric ratio. Curing kinetics have been carried out by differential scanning calorimeter (DSC). The presence of PC accelerates the curing reaction. Infrared spectroscopy (IR) indicates the occurrence of transesterification in the PC-DER331/MPDA blends during curing. The flexural modulus increases with the increase of the PC content while the notched Izod impact strength decreases with the increase of the PC content for all the blending systems. The fracture surfaces of the PC-DER331/MPDA blends are smooth, an indication of a homogeneous morphology. The fracture surfaces of the PC-DER332/MPDA blends are rough, an indication of a heterogeneous morphology.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 6 (1999), S. 259-266 
    ISSN: 1572-8935
    Keywords: Poly(trimethylene terephthalate) ; Melting behavior ; Crystallization ; Differential scanning calorimetry ; Double melting endotherms
    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 crystallization and melting behaviors of poly(trimethylene terephthalate) (PTT) have been studied by differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), and solid-state NMR. At certain crystallization temperatures (Tc) for a given time, the isothermally crystallized PTT exhibits two melting endotherms, which is similar to that of PET and PBT. At higher crystallization temperature (Tc = 210 °C), the low-temperature endotherm is related to the melting of the original crystals, while the high-temperature endotherm is associated with the melting of crystals recrystallized during the heating. The peak temperatures of these double-melting endotherms depend on crystallization temperature, crystallization time, and cooling rate from the melt as well as the subsequent heating rate. At a low cooling rate (0.2 °C/min) or a high heating rate (40 °C/min), these two endotherms tend to coalesce into a single endotherm, which is considered as complete melting without reorganization. WAXD results confirm that only one crystal structure exists in the PTT sample regardless of the crystallization conditions even with the appearance of double melting endotherms. The results of NMR reveal that the annealing treatment increases proton spin lattice relaxation time in the rotation frame, T1ρ H, of the PTT. This phenomenon suggests that the mobility of the PTT molecules decreases after the annealing process. The equilibrium melting temperature (T m o ) determined by the Hoffman-Weeks plot is 248 °C.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 7 (2000), S. 21-28 
    ISSN: 1572-8935
    Keywords: Polypropylene-g-maleic anhydride ; poly(oxyethylene) ; phase behavior ; crystallinity
    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 A family of amphiphilic graft copolymers were prepared from a maleated polypropylene (PP-g-MA) and various crystalline poly(oxyethylene)-segmented amines of 1000 to 3000 molecular weight. Structurally, these copolymers consist of polypropylene (PP) backbone and several crystalline poly(oxyethylene) (POE) pendants in the structure. In the observation of their phase behaviors by using a differential scanning calorimeter (DSC), the interference between the POE segments and PP backbone was found. In a particular case (PP-g-MA/ED-2001), the heat of POE crystallization did not show off in the cooling curve of the DSC, but appeared during the consecutive heating process. Generally, heating and cooling patterns of the DSC analyses showed the shifts of melting and crystallizing temperatures, depending on the length and the termini of POE, from those of the starting materials— PP-g-MA and POE amines. The TGA and optical microscopy observation further supported the DSC analyses.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-8935
    Keywords: Polymer blend ; Reactive compatibilizer ; Compatibility ; ABS ; Nylon 6,6 ; Morphology
    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 Styrene-acrylonitrile-glycidyl methacrylate (SAG) copolymers with various glycidyl methacrylate (GMA) contents have been used to compatibilize the incompatible blends of acrylonitrile-butadiene-styrene (ABS) and nylon 6,6 (N66) by varying the blending sequences. When the epoxy group of SAG copolymer makes contact and reacts with the amine endgroup of N66, the resultant grafted products, SAG-g-N66, tend to reside at interface and act as compatibilizers of the blends. For a SAG copolymer with lower GMA content (SG2), a better compatibilized blend is achieved by sequential blending of the SAG2 with N66 then with ABS. When a higher GMA content SAG (SAG 10) is employed, on the contrary, a better compatibilized blend is obtained by preblending SAG10 with ABS then with N66. A grafted SAG-g-N66 molecule is considered as an effective compatibilizer when it anchors along the interface with the ungrafted SAG, or the SA segments, penetrating into the ABS phase while the branched N66 chains protruding into the N66 phase. The conventional one-step three-component blending usually results in less compatibilized blend than the properly selected sequential blending. The trend of mechanical properties observed closely match the compatibility of the blend in terms of domain size. However, the overall improvement of the resultant mechanical properties of the compatibilized blend over the uncompatibilized one is not substantial.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-8935
    Keywords: Blends ; PP/EPDM ; DBTT ; Plastic zone ; Hysteresis energy
    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 mechanical fracture and ductile-brittle transition (DBT) behavior, hysteresis phenomenon and the plastic zone size of polypropylene (PP) / ethylene-propylene-diene terpolymer (PP/EPDM) blends were investigated by varying EPDM content and notch radius under different temperatures. An increase in test temperature or rubber content in the PP/EPDM blend results in lower yield stress and Young's modulus. The ductile-brittle transition temperature (DBTT) of the notched impact strength decreases with the increase of the EPDM content. However, the DBTT is fairly independent of the notch radius. SEM morphologies of the fracture surfaces indicate that two separate modes, localized and mass shear yielding, work simultaneously in these blends. The plane-strain localized shear yielding dominates the brittle failure at lower temperatures, whereas the plane stress mass shear yielding dominates the ductile fracture at higher temperatures. The presence of EPDM rubber decreases the yield stress of the PP/EPDM blend due to the overlapping stress fields of adjacent particles, resulting in higher hysteresis energy. The relationships among the test temperature, hysteresis loss energy and the size of plastic zone are discussed in detail.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-8935
    Keywords: Epoxy ; Polycarbonate ; Transesterification ; Transamidation
    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 Bisphenol-A polycarbonate (PC) has been incorporated into epoxy resin cured with 4,4′-diaminodiphenyl sulphone (DDS) and 4,4'-diaminodiphenyl methane (DDM). IR spectra reveal that transesterification and transamidation occur between the carbonate group of PC and the hydroxyl group of cured epoxy resin for the DDM-cured system, and that only transesterification occurs for the DDS-cured system. Scanning electron micrographs (SEM) show no evidence of phase separation in these cured systems, which is an indication of full miscibility between the bisphenol-A monomers and PC-oligomers with the copolymer network. The mechanical strength and glass transition temperature (Tg) fluctuate with PC content, whereas the flexural modulus shows a steadily increasing tendency.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 2 (1995), S. 13-20 
    ISSN: 1572-8935
    Keywords: PC/PBT ; Jc ; Hysteresis energy ; ASTM E813-81 ; Fracture toughness
    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 J-Integral fracture mechanics based on an hysteresis approach has been previously demonstrated to be viable and simple experimentally. However, the optimum procedure to construct the J-R curve in terms of regression model and data-window has not yet been well defined. In this study, the fracture toughness of the PC/PBT blend has been investigated using the previously developed hysteresis method by seven regression models and three data-window ranges. The second order polynomial model results in the best data-fitting capability and moreconsistent Jc values than those higher order polynomial models or the linear regression model. The critical J values obtained from this second polynomial model using the same data-window as ASTM E813-81 standard are comparable to those obtained from the ASTM standards. The trend clearly shows thathigher Jc values are obtained when the range of data-window is increased. The close Jc values obtained from this hysteresis method and the ASTM E813-81 indicate that the determined critical displacement from this hysteresis method is indeed the onset of crack initiation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymer research 4 (1997), S. 91-99 
    ISSN: 1572-8935
    Keywords: Polymer blend ; PA6 ; PPE ; Epoxy ; Reactive compatibilizer ; Coupling agent
    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 A commercially available multi-functional epoxy monomer, phenolic novolac epoxy (PNE) resin, has demonstrated to be an effective reactive compatibilizer for the blends of polyamide-6 (PA6) and poly(2,6-dimethyl-1,4-phenylene ether) (PPE). It requires about 1/10 by weight relative to a typical conventional reactive compatibilizer to achieve same level of compatibilization in terms of mechanical property improvements. By acting as a coupler, this multi-functional epoxy can react with PA6 and PPE during melt blending and produces the desirable PA6-co-PNE-co-PPE mixed copolymers at the interface. This in situ-formed copolymer containing PA6 and PPE segments tends to reside at the interface between PA6 and PPE domains to reduce melt interfacial tension and enhance interface adhesion as an efficient compatibilizer of the PA6/PPE blends.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1572-8935
    Keywords: Cyclo olefin copolymer (COC) ; Monomer reactivity ratio ; Solid state NMR ; Spin-lattice relaxation time (T1p C)
    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 In this paper, we report the monomer reactivity on the copolymerization of norbornene and ethylene. The reactivity ratios for ethylene (M1) and norbornene (M2) are 18.5 and 0.035, respectively. Different copolymerization conditions can produce COC with different microstructures. A 13C NMR shift assignment in pentad sequences in copolymers has been obtained. More isolated polynorbornene or a micro-block length can be obtained using a low Zr/Al catalyst/co-catalyst ratio and at a lower NB/ethylene feed ratio. The T1p C decay curve shows two component decays in all resonance peaks. These two component decays come from different norbornene microstructures, while the block and alternative have similar T1p C values.
    Type of Medium: Electronic Resource
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