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  • 1
    ISSN: 0935-9648
    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
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0935-9648
    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
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0935-9648
    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
    Additional Material: 5 Ill.
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  • 4
    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: Polyspiroacetal polymers and copolymers derived from pentaerythritol, and glutaraldehyde were prepared and examined for physical properties. Elemental and infrared analyses support the polyspiroacetal structure. X-ray analysis indicates a range of 20-40% crystallinity. Dipentaerythritol was observed to influence in varying degrees the crystallinity, the solubility, and the optimum range of film curing conditions. Resins with more than 25% dipentaerythritol always crosslinked during polymerization. In addition, the variables influencing such resin properties as molecular weight and gelation were examined. Films crosslinked with pyromellitic dianhydride exhibited good flexibility and tensile strength. Moreover, their oxidative thermal stability was only slightly less than that of crosslinked poly(ethylene terephthalate).
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 2003-2023 
    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: At temperatures far below the heat distortion point, the dissipation factor (and therefore power factor) of epoxy resins is comparably low - in the order of 0.001-0.01. Internally flexibilized, polyester-modified resins may have higher loss tangents, in the order of 0.01-0.10, even at room temperature. At temperatures far above the heat distortion point, anhydride curing agents give lower dissipation factors than do amines or acids. With anhydride cures, the higher molecular weight resins investigated cure faster than the lower molecular weight resins, give lower elevated temperature power factors and loss tangents, and are tougher. With any hardener-epoxy resin system, the optimum elevated temperature power factor, weight loss on aging and heat distortion point will probably depend on a close examination of the optimum hardener/resin ratio.With certain anhydride-cured low molecular weight epoxy resin systems, an increased rate of cure and lower elevated temperature power factor may be obtained by use of a small amount of higher molecular weight (polyhydroxy) epoxy resin. Attempts to compare the effect on power factor of changing the hydroxyl groups to less mobile dipoles by acetylation were unsuccessful, since the resulting acetoxy groups changed the cure mechanisms. However studies with resins of different molecular weights indicated that the effect of hydroxyl content on elevated temperature power factor is subordinate to other effects such as the rigidity of the cured resin system, rate of cure and ionic impurities. Acetylation of hydroxyl-containing epoxy resins may inhibit cure with some curing agents, due to side reactions of the resulting acetoxy group with specific hardeners.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. 503-507 
    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 reaction of various dialdehydes and one diketone with pentaerythritol or pentaerythritol-dipentaerythritol mixtures, has produced a series of thermoplastic, Polyspiroacetal resins. These possess molecular weights up to 10,000, solubility in a limited range of solvents, and high melting points. Some of these, with an optimum amount of crosslinking, have produced transparent, tough, flexible films.
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 589-602 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model for case II diffusion into polymers is presented. The addition of stress terms to the Fickian flux is used to produce the characteristics progressive front. The stress in turn obeys a concentration-dependent evolution equation. The model equations are analyzed in the limit of small diffusivity for the problem of penetration into a semiinfinite medium. Provided that the coefficient functions obey two monotonicity conditions, the solvent concentration profile is shown to have a steep front that progresses into the medium. The formulas governing the progression of the front are developed. After the front decays away, the long time behavior of the solution is shown to be a similarity solution as in Fickian diffusion. Two techniques for approximating the solvent concentration and the front position are presented. The first approximation method is a series expansion; formulas are given for the initial speed and deceleration of the front. The second approximation method uses a portion of the long time similarity solution to represent the short time solution behind the front.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1055-1067 
    ISSN: 0887-6266
    Keywords: hydrogels, polyacrylamide, characterization of inhomogeneity in ; polyacrylamide, inhomogeneous hydrogels of ; gels of polyacrylamide in water, physical and structural characteristics of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The physical and structural properties of acrylamide gels have been characterized by osmotic deswelling, mechanical compression, and x-ray scattering. These properties vary considerably with the concentration of the crosslinking agent bisacrylamide, at fixed total monomers concentration (10% wt/wt water). In particular, changes in the properties appear more prominent at a crosslinking level of about 5-6% (wt bisacrylamide/wt monomers). The compression modulus of as-prepared and swollen gels passes through a maximum at this level of crosslinking. The swelling pressure curves can be separated into osmotic and elastic contributions of the gel network. The elastic part exhibits similar behavior to the compression modulus. The scaling of the osmotic part with the gel concentration varies with the degree of crosslinking, changing from 2.33 to 3.09. This indicates that the solvent power of water decreases with increasing crosslinking level, towards Φ conditions. The scattering patterns from the gels have been analyzed as arising from additive contributions from a homogeneous gel matrix, and embedded heterogeneities having a higher crosslinking density. These heterogeneities become much more prominent at the same level of crosslinking about 5-6%. Hysteresis observed in the sorption/desorption behavior of polyacrylamide gel suggests that further irreversible structural changes may occur at water activities lower than probed by osmotic deswelling. © 1992 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 9
    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.
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  • 10
    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
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