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  • 1
    Publication Date: 1995-01-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    Publication Date: 1998-07-23
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Publication Date: 1998-03-26
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 152-159 
    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
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2193-2206 
    ISSN: 0887-624X
    Keywords: multicomponent ; latex ; interpenetrating polymer networks ; IPN ; core/shell ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of novel structured latex particles with interpenetrating polymer network (IPN) cores and glassy SAN shells were developed in an attempt to investigate the feasibility of these polymers as both toughening and damping agents in thermoplastics. The IPN cores were composed of one impact part (polybutadiene based) and one damping part (acrylic based, with Tg around +10°C). The particle morphologies of these polymers were determined by TEM. The glass transitions and mechanical behavior of the polymers were characterized from DMS. The effect of different components on the final core/shell particle morphologies and mechanical properties was studied. The mechanical behavior of core/shell particles with IPN cores was also compared with that of separate core/shell and multilayered core/shell particles. In addition, normal core/shell synthesis (rubbery part first then the glassy part) and inverted core/shell synthesis (glassy part first then the rubbery part) were performed to provide another access for morphology control. It was found that the core/shell latex particles with poly(butyl acrylate) based copolymers are more miscible than poly(ethylhexyl methacrylate)-based copolymers. The high grafting efficiency of poly(butyl acrylate) plays an important role in governing phase miscibility. The latex particles synthesized by the inverted core/shell mode showed higher miscibility than the normal synthesized ones. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2193-2206, 1997
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 197-208 
    ISSN: 1042-7147
    Keywords: Interpenetrating polymer networks ; synthesis ; morphology ; phase diagrams ; poly(methyl methacrylate) ; nomenclature ; simultaneous interpenetrating networks ; phase separation ; metastable phase diagrams ; polyurethane ; gelation ; 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: An interpenetrating polymer network, IPN, is defined as a combination of two or more polymers in network form, at least one of which is polymerized and/or crosslinked in the immediate presence of the other(s). The synthesis, morphology and mechanical properties of recent works are reviewed, with special emphasis on dual phase continuity, and the number of physical entanglements that arise in homo-IPNs. The concepts of phase diagrams are applied, especially to simultaneous interpenetrating network phase separations and gelations. Recent engineering applications are discussed.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 195-195 
    ISSN: 1042-7147
    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
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  • 8
    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: In a model polyurethane/poly(methyl methacrylate) (PU/PMMA) system, the partitioning of unreacted methyl methacrylate monomer (MMA) is studied in the late stages of its polymerization, simulated by incorporating controlled amounts of MMA in otherwise fully cured simultaneous interpenetrating networks (SIN) samples. Glass transitions temperatures (Tg) were determined using dynamic mechanical spectroscopy and differential scanning calorimetry as a function of MMA content of the SINs. The lowering of Tg in each phase due to the plasticization effect of MMA is used to calculate a plasticization coefficient for each phase, finally allowing calculation of the partition coefficient of MMA between the two phases. It is found that the MMA monomer distributes itself almost uniformly across the two phases of the current SIN system, leading to speculation as to the locus of late SIN polymerization. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 2005-2013 
    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 toughness as a function of temperature of polycarbonate modified by blending with core-shell structured latex particles was evalated. Comparisons were made among a commercial core-shell latex (MBS), other core-shell (CS) latexes that incorporated a single component rubbery core, and a new class of interpenetrating polymer network (IPN) core-shell latexes with two elastomers in the core. Notched tensile tests differentiated among the blends in terms of their toughness. The most effective modifier at low temperatures was the commercial MBS latex. The CS latexes produced blends that were only slightly less tough than the MBS blends despite better dispersion of MBS and better adhesion to the matrix. The IPN blends were the least tough at low temperatures; however, at 25°C, a blend with IPN had the highest impact strength. Differences between CS and MBS blends were attributed to differences in the percent of butadiene-containing rubber and the chemical nature of the shell. A comparison among the CS latexes showed that increasing the acrylonitrile content of the shell increased the toughness, and increasing the rubber content or the gel fraction of the core increased the toughness. © 1996 Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 331-346 
    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: Any simultaneous interpenetrating network (SIN) synthesis contains three key events. These are gelation of polymer I, gelation of polymer II, and phase separation of polymer I from polymer II. Metastable phase diagrams of SINs are developed, in which the time occurrence of these three events is represented. A polyurethane/poly(methyl methacrylate) (PU/PMMA) system was chosen as a model. Polymerization kinetics were followed in situ for both PU and PMMA using Fourier Transform Infrared Spectroscopy (FTIR) with the aid of a heated demountable cell. Glass transitions of fully cured samples were determined by dynamic mechanical spectroscopy (DMS) and differential scanning calorimetry (DSC). Phase separation was determined by the onset of turbidity, and gelation of the first gelling polymer was determined by the sudden resistance of the system to flow. As a result, a metastable phase diagram was constructed for the four-component SIN system (the two monomers and their respective polymers) as a tetrahedron in three dimensions with the two monomers and two polymers at the four apexes. Phase separation and gelations of the two polymers are indicated by various surfaces. These surfaces intersect at lines and curves, representing unique conditions of an SIN synthesis, e.g., simultaneous gelation of both polymers, or simultaneous phase separation and gelation of polymer I, etc. These conditions are critical in terms of the development of the SIN morphology, dividing the reaction space into specific regions. Finally, it is shown how the tetrahedron diagram helps visualize the course of the three key events during SIN synthesis, and provides direction for controlling them. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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