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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 24 (1991), S. 1161-1167 
    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 21 (1988), S. 433-435 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 21 (1988), S. 436-441 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 3631-3636 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 7638-7644 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 984-992 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The response of a mesoscopic layered structure to deformation normal to the layers is prevalently accepted to occur by an undulation instability, a model which was developed for and tested extensively in liquid-crystalline systems. This model has been applied to a layered block copolymer melt by theoretical considerations [Z.G. Wang, J. Chem. Phys. 100, 2298 (1994)] and extended to alternating glassy/rubbery layers by simulation and theory [D.J. Read et al., J. Phys. D. 32, 2087 (1999)]. In both cases, an undulation instability at extremely small strain is predicted. In this study we investigate the deformation mechanism of a lamellar block copolymer structure, stretched in the direction perpendicular to the layers, by simultaneous in situ measurements of sample stress and elongation and two dimensional small-angle x-ray scattering, at a strain resolution of 0.5%. Deformed microstructures were also observed ex-situ with scanning probe microscopy. A styrene-butadiene-styrene triblock copolymer of total molecular weight 82 000 g/mol containing 45% styrene, was used. Specimens were deformed at ambient conditions, where the system is characterized as alternating glassy/rubbery layers, at the glass transition temperature (Tg) of polystyrene (PS) where the system is viscoelastic/rubbery and well above the Tg of polystyrene where the system is viscous/rubbery. At ambient temperature, the constraints on the rubbery layers due to covalent bonding to the glassy layers at the interface, do not allow any significant dilation of the layer spacing. The results indicate that the yield point in the mechanical response does not correspond to a critical undulation instability. Rather, the low-strain behavior is dominated by tilting of layers in the vicinity of defects. Deformation of the block copolymer melt, above the Tg of PS, causes the layers to dilate affinely with the macroscopic elongation. The stability of dilated layers with respect to tilting is explained by a model which considers the dominating influence of interfacial tension. The undulation instability is observed only during deformation at about the Tg of PS, in which the system can be described as alternating viscoelastic/rubbery layers. © 2001 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 94 (1990), S. 5308-5312 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 57-64 
    ISSN: 0887-6266
    Keywords: reversible gelation ; rigid polymer ; poly(γ-benzyl-l-glutamate) ; small-angle neutron scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gelation and gel-melting phenomena in semidilute isotropic solutions of poly(γ-benzyl-L-glutamate) (PBLG) in benzyl alcohol were studied by small-angle neutron scattering measurements, using a deuterated solvent, and by cryotransmission electron microscopy. The reversible gels are formed when the solution is cooled below the gelation temperature, and the gels melt upon heating. Hysteresis, of about 15°C, is observed between gelation and melting temperatures. In the isotropic solution, PBLG exists as isolated helices. Gelation is apparent as a large increase in the intensity scattered at low angles, signifying the heterogeneous microstructure of the gel. Direct visualization by electron microscopy of vitrified gel samples shows the formation of a microfibrillar network. The dimension of the observed microfibrils is about 10 nm. Upon melting, microstructural changes appear in a temperature range of about 10°C. The unique feature of the gel melting is that initially only the intensity in the mid-angle range decreases. This is interpreted as thickening of the microstructure due to melting of the thinner microfibrils. The final stage marks the melting of the thicker microfibrils. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1833-1841 
    ISSN: 0887-6266
    Keywords: polymer gels ; topological constraints ; osmotic deswelling ; polyelectrolytes ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Recent data on comparative osmotic deswelling of poly(acrylic acid) gels and solutions shows that the difference between osmotic pressure of the gel and of the solution, Pgel (c, f) - Psolution (c, f), taken at equal polymer concentration (c) and fraction of the ionized acrylic acid monomers (f), changes its sign from negative to positive as the concentration c increases; this effect is enhanced with increasing f whereby it is shifted toward lower concentrations. In order to explain this effect, a model is suggested for the elastic pressure of the gel network which takes into account the effect of topological constraints combined with the effect of network ionization. According to the model, the sign-change of Pgel - Psolution originates from the topological constraints on conformations of the network; the ionization of the network chains enhances this effect and shifts it to the concentration range of the experiment. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1833-1841, 1997
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 809-812 
    ISSN: 1042-7147
    Keywords: emulsion polymerization ; coagulum ; tribromostyrene ; styrene ; copolymers ; 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
    Notes: Coagulum formation in emulsion polymerization of tribromostyrene and also in its copolymerization with styrene has been shown to be due to thermal polymerization. The latter takes place in the monomer reservoirs, even in the absence of radical generating initiators, converting them into sticky particles which then form the undesired coagulum. The coagulum formation phenomenon can thus be remedied by reducing the thermal initiation level through a semi-batch emulsion polymerization method, by lowering the polymerization temperature, and reduction of the collision frequency of monomer/polymer particles.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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