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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 32 (1997), S. 3463-3468 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The in situ polymerization of methyl methacrylate (MMA) with poly(styrene-co-acrylonitrile) (SAN) was studied. The PMMA/SAN in situ polymerization blends obtained were examined by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), tensile tests and scanning electron microscopy (SEM). The blends with compositions of 95/5, 80/20, 70/30, and 60/40 in weight ratios were miscible and had a single phase structure. However, the 90/10 PMMA/SAN in situ polymerization blend obtained was inhomogeneous and had a two-phase structure; polymerization-induced phase separation occurred during the preparation process of the blend. Both tensile strength and elongation at break increase with increasing SAN content up to 30 wt%. The degradation temperature and thermal stability of PMMA increased remarkably on incorporation of SAN up to 30 wt%.
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  • 2
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The results of dynamic mechanical analysis reveal that crosslinked polyester resin (PER)/poly(ethylene oxide) (PEO) blends show a composition dependent glass transition temperature, Tg, which suggests that the blends studied are homogeneous in the amorphous state. The initial dynamic storage modulus, E', decreases with increasing PEO content up to 30 wt% in the blends, whereas E for both the 60/40 and 40/60 PER/PEO blends is close to that for the 80/20 PER/PEO blend and much larger than that for the 70/30 PER/PEO blend. The addition of crystalline PEO has a remarkable effect on the mechanical properties of crosslinked PER. Tensile testing shows that the elongation at break first increases greatly and then decreases slightly, whereas the Young's modulus and the tensile strength first decrease and then increase slightly with increasing PEO content in the blends. The variation of tensile properties was considered to be due to both the plasticization effect and the crystallization effect of PEO in the blends. The impact strength remains almost unchanged with increasing PEO content in the blends studied. No dramatic decrease of thermal stability for PER/PEO blends was observed for the blends with PEO content up to 30 wt%.
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  • 3
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Poly(styrene-co-acrylonitrile) (SAN) was found to be miscible with the tetraglycidylether of 4,4'-diaminodiphenylmethane (TGDDM), as shown by the existence of a single glass transition temperature (T g) over the whole composition range. However, SAN was found to be immiscible with the 4,4′-diaminodiphenylmethane (DDM)-cured TGDDM. Dynamic mechanical analysis (DMA) shows that the DDM-cured TGDDM/SAN blends have two T gs. A scanning electron microscopy (SEM) study revealed that all the DDM-cured TGDDM/SAN blends have a two-phase structure. The fracture toughness K IC of the blends increased with SAN content and showed a maximum at 10 wt% SAN content, followed by a dramatic decrease for the cured blends containing 15 wt% SAN or more. The SEM investigation of the K IC fracture surfaces indicated that the toughening effect of the SAN-modified epoxy resin was greatly dependent on the morphological structures.
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  • 4
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 11 (1990), S. 279-283 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 211-218 
    ISSN: 0887-624X
    Keywords: poly(N-phenyl-2-hydroxytrimethylene amine) ; poly(∊-caprolactone) ; poly-(ethylene oxide) ; poly(vinyl methyl ether) ; polymer miscibility ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new polymer with pendant hydroxyl groups, namely, poly(N-phenyl-2-hydroxytrime-thylene amine) (PHA), was synthesized by a direct condensation polymerization of aniline and epichlorohydrin in an alkaline medium. The new polymer is amorphous with a glass transition temperature (Tg) of 70°C. Blends of PHA with poly(∊-caprolactone) (PCL), as well as with two water-soluble polyethers, poly(ethylene oxide) (PEO) and poly(vinyl methyl ether) (PVME), were prepared by casting from a common solvent. It was found that all the three blends were miscible and showed a single, composition dependent glass transition temperature (Tg). FTIR studies revealed that PHA can form hydrogen bonds with PCL, PEO, and PVME, which are driving forces for the miscibility of the blends. © 1997 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 401-411 
    ISSN: 0887-624X
    Keywords: novolac resin ; poly(ethylene oxide) ; interpolymer complexes ; crosslinkable ; polymer morphology ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crosslinkable interpolymer complexes of novolac resin and poly(ethylene oxide) (PEO) were prepared by mutual mixing ethanol solutions of novolac and PEO. Fourier transform infrared (FTIR) studies revealed that the driving force for the formation of novolac/PEO complex is hydrogen bonding interaction between the hydroxyl groups of novolac and the ether oxygens of PEO. The morphology and thermal properties of the complexes before and after curing were investigated by optical microscopy and differential scanning calorimetry (DSC). It was found that the uncured novolac/PEO complexes had a single composition-dependent glass transition temperature (Tg). The curing with 15 wt % hexamine (HMTA) (relative to novolac content) resulted in disappearing of Tg behaviour for both the neat novolac and the novolac-rich complexes, owing to less mobility of the novolac chain segments. The melting temperature (Tm) and crystallization rate of the HMTA-cured novolac/PEO complexes decreased with increasing novolac content, and no Tm was observed for the cured complexes with PEO content less than 50%. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 401-411, 1998
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3161-3168 
    ISSN: 0887-624X
    Keywords: unsaturated polyester resin ; poly(ethylene oxide) ; polymer blend ; polymer miscibility ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The miscibility and thermal properties of polyethylene oxide(PEO)/oligoester resin (OER) blends and PEO/crosslinked polyester (PER) blends were studied by differential scanning calorimetry (DSC). The effect of quenching process on the crystallization behavior of PEO for these two systems were investigated and discussed in details. It has been found that a single, composition dependent glass transition temperature (Tg) was observed for all the blends, indicating that the two systems are miscible in the amorphous state at overall compositions. From the melting point depression of PEO, the interaction parameter χ12 for PEO/OER blends and that for PEO/PER blends were found to be -1.29 and -2.01, respectively. The negative values of χ12 confirmed that both PEO/OER blends and PEO/PER blends are miscible in the molten state. Quenching process has a greater hindrance on the crystallization of PEO/OER blends than on that of PEO/PER blends. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3161-3168, 1997
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3169-3179 
    ISSN: 0887-624X
    Keywords: unsaturated polyester resin ; poly(ethylene oxide) ; hydrogen-bonding interaction ; polymer blend ; polymer morphology ; crystallization kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrogen-bonding interaction between the two components of the poly(ethylene oxide) (PEO)/oligoester (OER) blends and the PEO/crosslinked unsaturated polyester resin (PER) blends was found to be an important driving force to the miscibility of these polymer blends. Its strength is approximately as strong as the self-association of hydroxyl groups in either the pure OER or the pure PER. The crystallization kinetics and morphology of PEO in PEO/PER blends was remarkably affected by crosslinking. It was found that the overall crystallization rate of PEO in PEO/PER blends is larger than that in PEO/OER blends at the crystallization temperature investigated, which was considered to be the result of nucleation controlling mechanism. With decreasing PEO content, the regular shape of PEO spherulites turns irregular in PEO/OER blends, whereas in PEO/PER blends, the birefrigent spherulites turns into dendritic structures. Raising the crystallization temperature favors the formation of dendritic textures in PEO/PER blends. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3169-3179, 1997
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 315-322 
    ISSN: 0959-8103
    Keywords: poly(N-vinyl-2-pyrrolidone) ; novolac resin ; interpolymer complexes ; polymer blends ; crosslinking ; 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 formation of complexes between poly(N-vinyl-2-pyrrolidone) (PVP) and novolac resin in various solvents was studied. Interpolymer complexes were formed in methanol, ethanol, 2-butanone, cyclohexanone and N,N-dimethylformamide (DMF). However, only polymer blends were obtained in N-methyl-2-pyrrolidone. The nature of the solvent has a profound influence on the degree of interpolymer association. The formation of 1/1 and 2/1 ([novolac]/[PVP]) interpolymer complexes in DMF solution was shown by measurements of reduced viscosity, conductivity and clear point. Differential scanning calorimetry revealed the single-phase nature of both the blends and the complexes of uncured novolac/PVP. The complexes had higher glass transition temperatures than those of the blends with the same composition, and the strength of the interactions between the components in the complex is much higher than that in the blend. The driving force in the formation of the interpolymer complexes between novolac and PVP is the hydrogen-bonding interaction between the hydroxyl of the novolac and the proton-accepting groups of PVP. Both the blends and the complexes were cured with 15 wt% hexamethylenetetramine relative to novolac content. The cured novolac/PVP blends were only partially miscible, but significant amounts of complex still existed in the cured complexes. Fourier transfer infrared spectroscopy revealed that the interaction between the components was rather strong for both the uncured and cured blends.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 2111-2116 
    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: A study has been made of the crystallization behavior of polypropylene (PP) filled with rare earth oxides under isothermal conditions. These rare earth oxides include lanthanum oxide (La2O3), yttrium oxide (Y2O3), and a mixture of rare earth oxides containing 70% Y2O3 (Y2O3-0.70). A differential scanning calorimeter was used to monitor the energetics of the crystallization process from the melt. During isothermal crystallization, dependence of the relative degree of crystallinity on time was described by the Avrami equation. It has been shown that the addition of any of the three rare earth oxides causes a considerable increase in the overall crystallization rate of PP but does not influence the mechanism of nucleation and growth of the PP crystals. The analysis of kinetic data according to nucleation theories shows that the increase in crystallization rate of PP in the composites is due to the decrease in surface energy of the extremity surfaces. The relative contents of the β-form in the composites are somewhat higher than that in the plain PP. However, the contents of the β-form in the plain PP and the composites are all very low relative to those of the β-form and the influence of the formation of the β-form on the crystallization kinetics can be neglected. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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