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  • 1
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract At 298.15K, intrinsic viscosity [η] has been measured for poly (vinylpyrrolidone), PVP, samples of different relative molar masses M in pure water and eight different binary solvents. These solvents were water/acetone mixtures having different volume fractions of acetone (ACT). The solvation power of these mixtures showed a cosolvancy effect. The maximum solvation power was found for the mixture containing 0.2 volume fraction of ACT. The value of Kθ=74×10-3 dm3kg-1 was utilized for calculating the unperturbed dimensions, u.d., steric factor, σ, the characteristic ratio, C∞, and the persistence length, ap. Values of 0.666 Ao, 2.28, 10.38 and 8.76 Ao, respectively, were obtained for PVP in theta-solvent. The calculated values of the effective radius (Re), effective unit length (b) and the effective hydrodynamic radius of monomeric unit (ro) showed the complete impermeability of polymer molecules. Some errors in the polymer handbook and CRC, water-soluble synthetic polymers, were demonstrated with its logical corrections.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 26 (1991), S. 237-244 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary A spin labelled poly(decamethylene terephthalate) where the label is covalently bound into the aliphatic chain, has been studied by EPR spectroscopy. The motion of the label is strongly anisotropic at low temperatures, probably due to the extended all-trans conformation of the alkyl chain. The anisotropy of the label rotation decreases with increasing temperature. Two approaches to analyse the spectra at high temperatures are presented.
    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. 1107-1114 
    ISSN: 0887-6266
    Keywords: polyelectrolytes ; conformational change ; water-acetone mixture ; viscosity and conductivity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Samples of a polyelectrolyte poly(methacryloylethyl trimethylammonium methylsulfate), PMETMMS, with molar masses Mw = 22-25 × 106 were examined with viscosity, static light scattering, and conductivity measurements in a water-acetone solvent. Because acetone is a nonsolvent for this polymer the measurements were performed to determine the influence of the solvent composition, the polymer concentration, and the presence of added ions on the conformation of the polyelectrolyte in mixed solvents. The possible influence of a hydrodynamic field on the polymer conformation was also studied. The viscosity of the polymer solutions as a function of polymer concentration, as well as of the solvent composition, was studied using a broad range of shear rates. When the mass fraction of acetone in the solvent, γ, is below 0.5, the solutions show a usual polyelectrolyte behavior. When γ ≥ 0.80, the polymer adopts a compact conformation. This is observed as a decrease of the radius of gyration, Rg, second virial coefficient, A2, the viscosity, and also as a change in the conductivity of the solution. The change in the polymer conformation may be induced also by dilution. When 0.60 ≤ γ 〈 0.80, a gradual decrease in the polymer concentration leads to a sudden decrease of the reduced viscosity, which indicates a decrease in the particle size. The values of Mw measured by static light scattering were constant in all experiments. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1107-1114, 1998
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 55-64 
    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: Styrene has been copolymerized with various bifunctional poly(dimethyl siloxane) cross-linkers having molar masses in the range 200-35,000. Calorimetric and rheological measurements show that the crosslinkers change Tg, Tll, and Texo, as well as melt viscosity and elasticity of polystyrene. These changes are strongly dependent on the molar mass of the crosslinker. Increasing the length of the siloxane crosslinker lowers Tg and melt viscosity, if the molar mass of the crosslinker is in a range 200-2000. Copolymerizing styrene with a bifunctional poly(dimethyl siloxane) having molar mass near 35,000 leads to a phase-separated polymer where polystyrene phase largely retains its original properties.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 2011-2019 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Aqueous solutions of poly(N-vinyl-2-pyrrolidone) are converted to gels by reaction with potassium peroxydisulfate K2S2O8. The degree of crosslinking in the gel fractions depends on the amount of persulfate used. The degree of crosslinking is related to the amount of non-freezing bound water in the gels by means of differential scanning calorimetry in the temperature range from -50°C to + 170°C. The chemical nature of the bonds formed during gelation is studied by 1H and 13C NMR Spectroscopy and by swelling tests. NMR measurements point to the formation of aliphatic sidechains as well as crosslinks in the gelation. The swelling tests give low values for the number of crosslinks, hence the formation of branched chains strongly influences the properties of the gels. In contrast to what was expected no carboxyl groups are found in the gels.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 1099-1106 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Spin-lattice relaxation times (T1) have been measured by 13C NMR for poly(vinyl alcohol), poly(vinyl benzoate), poly(vinyl cinnamate) and poly(vinyl acetate) in dimethyl sulfoxide as a function of temperature and concentration. As expected, T1 increases with increasing temperature and decreases with increasing polymer concentration. The influence of the microstructure (tacticity) of the polymers on the relaxation times is negligible. T1 for the methine carbon of the polymer main chain is observed to serve as a measure of the rigidity and/or mobility of the chain. Assuming isotropic motion of the polymer chains, the activation energies for the protonated carbons were determined using the calculated correlation times.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2141-2152 
    ISSN: 0887-6266
    Keywords: N-isopropylacrylamide ; fluorocarbon-containing comonomers ; linear latices ; microgel ; hydrophobicity and hydrophilicity ; transition heat ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of thermally responsive copolymers of N-isopropylacrylamide (NIPAAM) with a fluorinated hydrophobic comonomer, either hexafluoroisopropylmethacrylate (HFIPMA) or 2,2,3,3,4,4-hexafluorobutylmethacrylate (HFBMA) and a hydrophilic comonomer, methacrylic acid (MAA), were synthesized by emulsion polymerization. The chemical structures of the copolymers were studied by the IR technique. Dynamic light scattering (DLS) showed that aqueous latices of the copolymers exhibited swelling-deswelling changes typical to PNIPAAM; the degree of swelling as well as the temperature at which the polymers collapse depended on the chemical structure of the comonomers. Endotherms related to the contraction of the polymers were studied by differential scanning calorimetry (DSC). A combination of DLS and DSC results revealed that the hydrophobic and hydrophilic units in the copolymers strongly affected the swelling behavior, as well as the local environment of the PNIPAAM chains. The comonomer HFIPMA increased the hydrophobicity of NIPAAM, reduced the swelling, and caused coagulation of the copolymer of NIPAAM and HFIPMA at temperatures above the critical temperature. Hydrophobicity of HFIPMA also affected the rheological properties of the latex. The HFBMA comonomer increased the swelling of the latex particles. Methacrylic acid added into the associating copolymers made the copolymers to show polyelectrolyte behavior with an increase of swelling and a decrease of the enthalpy change upon the collapse. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2141-2152, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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