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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2623-2634 
    ISSN: 0887-6266
    Keywords: interface ; surface tension ; rheological ; morphology ; polymethylmethacrylate ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Impact modifiers with grafted PMMA shell are used to modify polymethylmethacrylate matrix. The composition of the shell is chosen to enhance the interactions at the modifier/matrix interface and to obtain good dispersion of the impact modifier in order to optimize impact strength of the blend. The degree of interactions at the interface is characterized by the interfacial region where the chains of the matrix mix with those of the shell of the modifier. The deviation of the measured viscoelastic behavior of these blends from that predicted by the emulsion models has been attributed to the formation of the network structure due to the association of matrix chains with the shell of the modifier. It is expected that the network structure will decrease with increasing frequency and, as such, the effective volume of the particle is frequency dependent. This study uses the emulsion models to estimate the larger effective volume of the particle and, therefore, the extent of interaction at the interface. In the blends of this study it can be shown that at low modifier levels the solvent swelling of the modifier shell results in stronger interactions with the matrix; this effect is negated by the aggregation of particles at higher modifier loadings. The interaction of core modifier with the PMMA matrix seems to be similar to that of the core-shell modifier. This would not be expected from the calculated interfacial thickness of approximately 4 nm. It is, therefore, proposed that during melt-processing the core modifier surface was altered due to grafting of the matrix PMMA chains during melt-blending to (BA/St) copolymer of the core modifier thus reducing the interfacial tension. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2623-2634, 1998
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 2305-2318 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have investigated the optical rotatory dispersion of a stereo-irregular polyelectrolyte when neutralized with alkaline and N-tetraalkylammonium hydroxides, both in water and aqueousacetone mixtures.The variations of the optical activity properties during the neutralization can be well related to potentiometric and viscosity measurements. They are interpreted by assuming two kinds of solvation of the chiral centers located on the main chain, to which two partial optical rotary dispersions (ORD) of opposite signs are associated. The observed optical activity changes and specifically the discontinuity occurring in the neutralization range where a conformational transition between a compact structure and a more extended one is initiated, are thus accounted for in terms of the corresponding changes in the state of solvation of chains.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 193-202 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Potentiometric titrations in water of high-molecular-weight partly hydrolyzed polyacrylamides were analyzed by the Lifson - Katchalsky rodlike model. A fair concordance was found between theory and experimental curves with pK0 of acid functions of about 4.75 when 0 〈 τ 〈 0.49. Two methods were derived to calculate the parameter n of the extended Henderson-Hasselbach equation by using a series expansion of pKa vs. α, not yet reported in the literature. A new equation for n was established and comparison between two sets of values of n, obtained by using the theoretical ΔpK curves and series expansion is discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 659-672 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ionization (α) and added salts (NaCl, CaCl2, MgCl2) on the dimensions of commercially available high-molecular-weight polyacrylamides (Mw ≃ 4 × 106), hydrolyzed at various extents (0.04 〈 τ 〈 0.49) and which have been characterized, was investigated by viscosity and light-scattering measurements performed at 25°C. The data point with evidence to the strong dependence of the chain dimensions on the charge density (ατ) and the effect of the nature and concentration of added salts. From a practical point of view it is shown that there is no advantage to using too highly hydrolyzed samples (τ 〉 0.45) in media containing large amounts of salts that lead to precipitation of polymers, especially in the presence of divalent ions.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 77-87 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction between polyelectrolytes and Acridine Orange (AO) has been investigated in the case of poly(acrylic acid) (PAA), poly(methacrylic acid) (PMA), and a polycondensate between 1,3-benzene disulfonyl chloride and L-lysine (PLL) by visible absorption and fluorescence spectroscopy. The influence of both polymer ionization and polymer/dye ratio (P/D) on the spectral behavior of the bound dye has been studied. The stacking tendency of AO is found lower in the presence of PLL under compact conformation (in an ionization range depending on the nature of the counterion) with correlated enhancement of the green fluorescence of the monomeric species of the bound dye. The disappearance of the green fluorescence and the dimerization of bound AO are directly related to the increased flexibility of polyion chains upon ionization. Some analogy is found between the behavior of bound AO in the presence of very compact PLL chains and that reported for AO in the presence of native DNA, which might be due to specific interactions responsible for a kind of “intercalation” of the monomeric bound dye.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 4011-4020 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of polymer conformation, polymer concentration, and added salt concentration on the quantum yield φ of Auramine O (AuO) is discussed in connection with dialysis equilibrium data. The quantum yield per bound dye molecule (φ/q) assumes different values which are related principally to solvation changes in the environment of the binding sites. Binding to globular compact a states results in high φ/q, whereas low φ/q (of the order of magnitude of φ of free AuO) are observed for the binding to expanded solvated b states. The quantum yield of bound AuO is therefore affected by the organic nature of the environment, but shows little or no relation to the amount of bound dye molecules.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1367-1373 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the induced Cotton effects in the visible region of the absorption bands of acridine orange in the presence of a nonstereoregular α-carboxylic polysulfonamide (PLL) can be attributed to stacked bound dye molecules, irrespective of the conformation of the polymer. The existence of an ordered structure seems to be unnecessary for such an induction.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of urea and of dyes on the viscometric behavior of aqueous solutions of PLL has been investigated. The compact structure, which is characteristic of PLL in pure water, is found to disappear progressively as the amount of urea is increased. This is interpreted as due to the destruction in such media of nonelectrostatic interactions responsible for the stabilization of the compact structure of PLL in pure water. In 8M urea, the macromolecular behavior of PLL during the ionization is dependent only on the repulsive interactions between the charged groups. The extension of PLL is then practically independent of the nature of counterions, contrary to what was observed in pure water. In the presence of dye (acridine orange), the compact form of PLL is stabilized, and the dye is found to bind for the two structures of PLL. The analogy between the behavior of Bu4N+ and that of dye is in agreement with the fact the Bu4N+ leads to a stabilization of the compact structure by way of specific interactions between N-tetraalkylammonium counterions and the PLL chain through the structure of water. The hydrodynamic behavior of PLL is in good agreement with data obtained from potentiometric and optical activity measurements.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 327-336 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interaction between 2-p-toluidinylnaphthalene-6-sulfonic acid (TNS), a hydrophobic fluorescent probe, and poly(2-vinylpyridinium) polyions (PVP) has been investigated by fluorescence spectroscopy. Both the effect of the charge and the concentration of PVP on the fluorescence behavior of TNS indicate that interaction between TNS and hydrophobic sites present in the PVP chain is responsible for the observed phenomena. It is shown that PVP which exists with predominant hydrophobic regions leads to TNS fluorescence, but some residual charge must be present to facilitate the penetration of the dye into the hydrophobic regions. Various situations existing in some polyelectrolyte systems are discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2767-2778 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ionization on the potentiometric and viscometric behavior of both poly(methacrylic acid) (PMA) and poly(acrylic acid) (PAA) was investigated in methanol-water mixtures. The potentiometric and viscosity data revealed that the conformational change which takes place for PMA in water gradually disappears with increasing content of methanol in methanol-water mixtures. For mixtures containing 40 and 50% methanol, the behavior of PMA solutions becomes similar to that of PAA, i.e., the discontinuity versus the degree of ionization is no longer detectable and the molecule unfolds regularly upon ionization. The addition of methanol leads to the breakdown of the compact structure of PMA which is stabilized, at low degree of ionization in water, by nonelectrostatic interactions between the methyl groups of PMA.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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