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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 6365-6367 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 5108-5110 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1536
    Keywords: Polystyrene(1)/poly(butyl acrylate-methacrylic acid)(2) ; core-shell ; morphology ; latex films ; phase arrangement ; mechanical properties ; differential thermal analysis ; scanning electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polystyrene(1)/poly(n-butyl acrylate-methacrylic acid)(2) structured latex particles were prepared through a two-stage emulsion polymerization procedure, using a polystyrene (PS) latex seed (118 nm), and differentn-butyl acrylate (BA)/methacrylic acid (MAA) ratios. Polymerization kinetics, particle morphology, and MAA location have already been discussed in the first part of this series. In this second part the thermomechanical behavior of films cast from these latexes was studied. Differential Thermal Analysis and Dynamic Mechanical Analysis (DMA) were employed as characterization techniques for the films. Two polymer phases corresponding to polystyrene and a poly(BA-MAA) copolymer were distinguished. Comparison was made to analogous unfunctionalized PS/PBA systems, as a result of which an effect of MAA upon the phase arrangement in the film was found. Scanning Electron Microscopy of film samples and DMA showed that the evolution of the phase arrangement as a result of annealing was strongly dependent on the type of mechanical and heat treatments being applied to functionalized systems. Finally, the thermomechanical behavior of films was related to the structural features of the corresponding latexes, and computer simulation techniques wer eemployed to establish a mechanistic support for these relationships.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1436-2449
    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: Summary A rubbery (CTBN based) thin layer is added onto the surface of glass beads embeded in a DGEBA — DDA matrix. The chemical and the coating processes are described. The existence of a specific relaxation of the interphase is evidenced using viscoelastic measurements. The presence of an other α1 relaxation is discussed.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1536
    Keywords: Polystyrene seed ; poly(butyl acrylate-methacrylic acid) shell ; particle mophology ; location of carboxylic groups ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polystyrene (PS) (1)/Poly(n-butyl acrylate (BA)-methacrylic acid (MAA)) (2) structured particle latexes were prepared by emulsion polymerization using monodisperse polystyrene latex seed (118 nm) and different BA/MAA ratios. Three main aspects have been investigated: i) the polymerization kinetics; ii) the particle morphology as a function of reaction time; iii) the distribution of MAA units between the water phase and the polymer particles. The amount of MAA in the shell copolymer was found to be the main factor controlling the particle shape and morphology. The shape of the structured particles was, generally, non-spherical, and the shape irregularities increased as a particles was, generally, non-spherical, and the shape irregularities increased as a function of reaction time. At the beginning of the second stage reaction, new small particles were observed, which coalesced onto the PS seed as the polymerization proceeded. The distribution of the MAA groups in the latex particles and the serum was analyzed by alkali/back-acid titration, using ionic exchanged latexes. No MAA groups were detected in the latex serum. Due to the lowTg of the BA-MAA copolymers, alkali conductimetric titrations accounted for all the MAA groups on and within the polymer particles. Therefore, for these systems, this method is not only limited to a thin surface layer, as it is often assumed.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1435-1536
    Keywords: Cellulose ; poly(vinyl pyrrolidone) ; polymer blend ; scanning electron microscopy ; dynamic mechanical analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract New polymer blends based on cellulose and poly(vinyl pyrrolidone) (PVP) were obtained using a mixture of N=methyl morpholine N-oxide (NMMO) and dimethylsulfoxide (DMSO) as a common solvent system. Materials are obtained after the removing of NMMO-DMSO in three of their different solvents, namely i) H2O, ii) a mixture 95/5 vol/vol hexamethyl phosphororri amide (HMPA) DMSO and iii) a mixture of 95/5 vol/vol dioxan/water. Scanning electron microscopy techniques were extensively used and lead to the conclusion that all these blends in the composition range 25/75 w/w to 75/25 w/w cellulose/PVP are two-phase systems in which cellulose forms a continuous phase. Preliminary results from calorimetric and dynamic mechanical measurements confirm these observations. Furrthermore, it is shown that using dioxanwater preserves the initial cellulose PVP composition, allowing to get blends with the desired PVP fraction. Although it is not the case with HMPA/DMSO which dissolves a part of PVP, its use leads to assymmetric, porous structures.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1435-1536
    Keywords: PS latexes ; PBA latexes ; polymer blends ; mechanical relaxations, percolation ; coalescence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The emulsion polymerization process allows production of polymer particles with different structural morphologies. Films obtained after coalescence keep some memory of this morphology, but large modifications can occur during coalescence. In the present case, one of the polymers, polystyrene (PS), exhibits a glass temperature (Tg) much higher than the filmification temperature (close to room temperature), while the other one, poly(butyl acrylate) (PBA), has a much lowerTg. Furthermore, it is well known that dynamic mechanical measurements can be very helpful in providing information on the morphology of polymer materials, i.e., on geometrical and topological arrangement of homopolymer domains. At first, this method was used for comparison of two types of films: i) the first one obtained from structured-core (PS)-shell (PBA) particles, ii) the second one obtained from a blend of homopolymer particles (PS and PBA). It appears that the expected core-shell particles lost their geometric structure in the second film. Second, comparison of the predicted dynamic modulus and experimental data shows that i) strong interactions exist between PS nodules unless their coalescence has occured, leading to an abnormally high modulus at room temperature, ii) after achieving their coalescence, PS forms a more or less continuous phase. Both phenomena strongly depend on the particle size and their respective volume fractions.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1435-1528
    Keywords: Key words Cellulose ; N-methylmorpholine N-oxide (NMMO) ; rheology ; processing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Steady-state and dynamic experiments have been performed on solutions containing cellulose dissolved in monohydrate of N-methylmorpholine N-oxide (NMMO). The dependence of the zero-shear viscosity η0, and of the terminal relaxation time τ c , on concentration, average degree of polymerization (DP) and temperature are discussed. The behavior of this semi-rigid, polymolecular polymer in solution differs from that of flexible monodisperse ones. The slope of the plot of log(η0) versus, on the one hand, log(c) at fixed molecular weight (DP)=600, and, on the other hand, log(DP) at fixed concentration (c=5%w/w) are equal to 4.6 and 5 respectively, instead of 3.4 in the concentrated region. Experimental data for the shear modulus were fitted using the classical Doi-Edwards equation with a log normal distribution of relaxation time. This distribution is compared to the distribution of DP.
    Type of Medium: Electronic Resource
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  • 9
    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 microstructure and mechanical properties of polyamide 12/isotactic polypropylene blends with different compositions are studied. It is shown that the injection moulding technique used to process all samples results in a more or less pronounced orientation of macromolecular chains, which in its turn is responsible for a preferential orientation of polymer crystals. At a larger scale, the injection technique is also responsible for the deformation of polyamide domains into ellipsoides when polypropylene is dominant. In contrast, when polyamide is dominant, domains of both polymers are co-continuous in the materials. This feature is discussed on the basis of dynamic mechanical measurements.
    Type of Medium: Electronic Resource
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  • 10
    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 Evolution of a.c. electrical properties under large strain of random nanocomposite materials made of a soft thermoplastic insulating matrix and hard conductive fillers is investigated. The transport properties are directly linked with the macroscopic mechanical strain on the composites during uniaxial tensile test or to the time under relaxation, meaning that the method is suitable for monitoring microstructural evolution of such composites. The real part of the conductivity indicated the breaking of the percolating network, while the imaginary part gave information on the possible “spatial correlation” of the damage events. Two different filler shapes were used, i.e. spherical and stick-like (aspect ratio about 15), leading to quantitatively different results. The microstructural evolution was simulated with the help of a resistance–capacitance (RC) model for the electrical properties and with finite element analysis for the mechanical properties.
    Type of Medium: Electronic Resource
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