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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1285-1294 
    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: High quality packaging films from hydroxyethyl cellulose of low degree of substitution (DS) are being produced commercially in this country and abroad. Increasing demand for this and a variety of other applications requires a rapid and simple production control method for determining hydroxyethyl substitution of cellulose. None of the known analytical methods fulfills these requirements. The present paper describes a method which is based on the relationship between the solubility and the molar hydroxyethyl substitution of hydroxyethyl cellulose. A washed and dried sample of hydroxyethyl cellulose is dissolved in 7% aqueous sodium hydroxide. Methyl alcohol, a nonsolvent, is used to precipitate a fraction of the sample. The turbidity of the equilibrium system is determined and optical density readings are related to molar substitution. The method is most useful in low DS ranges of 2-8% EtO but is susceptile to broader application through adjustment of the composition of the solvent-nonsolvent mixture. Relatively large variations in DP can be tolerated. The molar substitution level of an hydroxyethyl cellulose sample can be obtained in 40 min. by this method, making it a practical production control technique.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 181-192 
    ISSN: 0887-6266
    Keywords: ternary solutions ; solvent quality ; polystyrene-dioctyl phthalate ; light scattering ; Boger fluid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymer solvent interactions in the ternary system high molecular weight polystyrene (HMPS), low molecular weight polystyrene (LMPS), and dioctyl phthalate (DOP) have been characterized by means of intrinsic viscometry (IV), dynamic light scattering (DLS), and static light scattering (SLS). Excluded volume exponents have been extracted from the scaling of intrinsic viscosity and translational diffusivity with polymer molecular weight for a mixed solvent of 13 wt % LMPS/87 wt % DOP. The value of the excluded volume exponent, v = 0.45, indicates that HMPS in the mixed solvent DOP/LMPS has apparently assumed a reduced conformation relative to the theta condition. However, SLS measures of the second virial coefficient (A2) confirm that DOP is a theta solvent at our experimental temperature of 22°C and indicate that the addition of LMPS increases A2. SLS also suggests that neither solvent component is strongly preferentially adsorped into the HMPS coil. Our system then is a mixture of a theta solvent and a good solvent that exhibits poor solvent scaling behavior. We believe this to be the first demonstration of such behavior in a system that does not exhibit appreciable preferential adsorption. We conclude by examining our observations in the context of current descriptions of mixed solvent thermodynamics. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    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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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the thermal decomposition of dimethyl-N-(2-cyano-2-propyl)ketenimine, DKI, in benzene solution over the 61-92°C. range have been investigated by means of proton magnetic resonance spectroscopy for quantitative analysis of reaction mixtures. The NMR equipment used comprised a Varian Model 3311 spectrometer, operating at a fixed radio frequency of 56.445 Mcycles/sec. and equipped with the Model V-K 3506 super-high-resolution field-stabilizing unit and the Model V-K 3507 slow-sweep unit. The kinetic data obtained tally closely with those reported earlier for a nitrometric and ultraviolet spectrophotometric study of the thermal breakdown of 2,2'-azobisisobutyronitrile, AZO, in the same solvent within the 60-80°C. range. Consequently the general mechanism assumed in interpreting the previous results for the AZO decomposition is confirmed. They also agree with all other comparable data available as well as expected. As a natural part of this study, it has been shown that NMR provides reliable and convenient methods of quantitative analysis of reaction mixtures when DKI or AZO is thermally decomposed. One variation of the analytical technique practiced involved comparison of the C13-sidebands in the NMR spectrum of a major constituent of a mixture with the main spectrum from a minor constituent. This was especially valuable for settling the initial purity of the DKI decomposed and the extent to which side products such as isobutyronitrile, methacrylonitrile, and 2,3,5-trimethyl-2,3,5-tricyanohexane were formed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 5 (1984), S. 203-208 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 5 (1984), S. 197-201 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 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 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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  • 8
    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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  • 9
    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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  • 10
    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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