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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 260 (1982), S. 678-684 
    ISSN: 1435-1536
    Keywords: Interpenetrating polymer network ; crosslinked polystyrene ; domain size ; 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
    Description / Table of Contents: Abstract A series of sequential interpenetrating polymer networks, IPN's, of poly(n-butyl acrylate) and polystyrene were prepared. A new equation predicting the domain size in IPN's is summarized and shown to yield agreement with the morphologies observed via scanning electron microscopy. The experimental variables required to determine the domain size include the volume fraction and crosslink level of each polymer, the interfacial tension and the temperature.
    Notes: Résumé Un nouveau modèle thermodynamique prédisant la taille des domaines des réseaux polymères interpénétrés préparés en deux étapes est décrite. Les paramètres influents sont la tension interfaciale et la densité de réticulation des deux polymères, ainsi que la composition. A l'aide de la microscopie électronique à balayage, la théorie a été vérifiée pour le système poly(acrylate den-butyle)/polystyrène.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 583-597 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Millar-type interpenetrating polymer networks (IPNs) are composed of two identical networks. In the present case Millar IPNs of polystyrene/polystyrene were prepared where the crosslinker levels of the two networks differed by a factor of 10. Polymer network I contained 0.4% divinylbenzene (DVB) and polymer network II contained 4% DVB, the polymers having the following weight proportions: 75/25, 50/50, and 25/75. A single polystyrene network containing 2.2% DVB was synthesized for comparison with the 50/50 Millar IPN, both containing the same average amount of crosslinker. The creep behavior of the Millar IPNs was found to be dominated by polymer network I, as were the rubbery moduli and swelling behavior in toluene. These results suggested that polymer I domains are more continuous in space and polymer II domains are less continuous. The Donatelli equation predicted polymer II domain sizes of 60 Å to 100 Å for the Millar IPNs. Electron micrographs of specimens containing 1% isoprene in polymer II offered visual evidence for the segregation of polymer II domains from polymer I, and showed that the polymer II domains were, in fact, less continuous. Polymer II domains varied from about 50 to 100 Å in size, as predicted. These results have implications for gelation processes in general.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 1597-1609 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two crystal modifications have been found for poly(3,3-bisethoxymethyl oxetane) [poly- (BEMO)] by wide-angle x-ray powder diffraction and differential scanning calorimetry, while only one modification has been found for poly(3,3-bisazidomethyl oxetane) [poly(BAMO)]. Melting temperatures for the two polymers were nearly the same, varying from about 70 to about 90°C depending on the thermal treatment; higher crystallization temperatures resulted in higher melting temperatures. The equilibrium melting temperature T*m was found to be 125 and 128°C for poly(BEMO) and poly(BAMO), respectively, by using the Hoffman-Weeks extrapolation procedure. Measurement of the melting-point depression of Poly(BEMO) and poly(BAMO) in dibutyl phthalate yielded enthalpy of fusion values of 2.25 and 12.8 kcal/mol, respectively. The percent crystallinity for poly(BEMO) and poly(BAMO), respectively, was calculated to be 55-60 and 13-30% based on DSC and x-ray analysis.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 259-263 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stress relaxation properties of poly(ethyl acrylate) and polydimethylsiloxane were investigated under conditions where oxidative degradation was minimized. The relaxation observed is thought to result from the continued approach to equilibrium of the network chains with cooperative thermal motion. These elastomers, representing two new classes of polymer, and two new types of crosslinking, were found to behave surprisingly like natural rubber and butadiene-styrene copolymer. Relaxation was found to obey a power law in time, with a negative exponent of 0.22 for both polymers.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 425-427 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1513-1523 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Six homologs of the cellulose triester series were found to exhibit, in general, three second-order transitions as determined dilatometrically. A parallel study of torsional modulus versus temperature revealed one glass-rubber transition, which allowed molecular assignment of one of the above. The dependence of the remaining two transition temperatures on length of the ester group permits some speculation with regard to their origin. The glass-rubber and secondary transitions exhibit an inversion for cellulose trivalerate and higher homologs, the two secondary transitions occurring at temperatures higher than the glass-rubber transition. A possible explanation for this anomaly in terms of side-chain crystallization is discussed.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1501-1514 
    ISSN: 0887-6266
    Keywords: multicomponent ; latex ; interpenetrating polymer networks ; IPN ; core/shell ; damping ; loss area ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The integrals of the linear loss shear modulus vs. temperature (loss area, LA) and linear tan δ vs. temperature (tan δ area, TA) were characterized for various core/shell latex particles with synthetic rubber, poly(butadiene-stat-styrene) [P (Bd/S), 90/10], and interpenetrating polymer networks (IPN) as the cores. The IPN cores were composed of P(Bd/S) (Tg ≃ - 70°C) and an acrylate based copolymer (Tg around 10°C) for potential impact and damping improvement in thermoplastics. Poly(styrene-stat-acrylonitrile) (SAN, 72/28) was the shell polymer for all these polymers. Under the same loading, for both toughening and damping controls, among the IPN core/shell, blend of separate core/shell, and multilayered core/shell polymers, the IPN core/shell polymers were the best dampers. However, the other core/shell polymers also showed higher LA values than P(Bd/S)/SAN core/shell polymer. A comparison of LA values via a group contribution analysis method was made, the effect of particle morphology and phase continuity on damping being studied. Inverted core/shell latex particles (glassy polymer SAN was synthesized first) showed much higher LA and TA values than normal core/shell ones (rubbery polymer was synthesized first). Models for maximum LA and TA behavior are proposed. The damping property was essentially controlled by the phase miscibility and morphology of the core/shell latex particles. The LA values for each peak in these multiphase materials provided some indication of the several fractional phase volumes. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1501-1514, 1997
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1973-1984 
    ISSN: 0887-6266
    Keywords: interpenetrating polymer networks ; simultaneous interpenetrating networks ; IPN ; SIN ; metastable phase diagrams ; epoxy-acrylate ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Simultaneous interpenetrating polymer networks (SINs) based on epoxy/poly(n-butyl acrylate) systems were synthesized at 120°C. The polymerization kinetics were studied both in situ by Fourier Transform Infrared Spectroscopy (FT-IR). Three key events occurred during the polymerization, namely the gelation of the network I, gelation of the network II, and phase separation of one polymer from the other. Thus, metastable phase diagrams describing the relations between the three events were constructed. Three-dimensional tetrahedrons characterizing the four-component system (the two monomers and the two polymers) allow the visualization of these three key events and also define some critical points, for example, the loci of the points where simultaneous gelation of the two networks occurs. The inside of the tetrahedron was also investigated using partially reacted model compounds. These tetrahedrons can be used as guidelines for setting up a synthesis strategy leading to desired morphologies. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1973-1984, 1997
    Additional Material: 11 Ill.
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