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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 1-8 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The alkaline hydrolysis of polyacrylamide in solution is studied viscosimetrically. The viscosity of the solution increases continuously during the course of hydrolysis. The relationship between intrinsic viscosity and the extent of reaction is established, using a series of polyacrylamides with known extents of hydrolysis. The extent of reaction is determined from the observed flowtime, using the relationship between [η] and extent of reaction. The second-order rate constant and the activation energy are in good agreement with those reported in the literature. A four-fold increased reactivity of the amide groups towards hydrolysis is observed at very low extents of hydrolysis.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 969-982 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Partially hydrolysed polyacrylamide samples were used as model polyelectrolytes and the variations of the intrinsic viscosities with the extent of hydrolysis and molecular weight were used to determine the relative applicability of the various macroion expansion theories. Expanison coefficients solely attributable to the presence of electrostatic charges were calculated with reference to the intrinisic viscosities of the parent polyacrylamides, assuming that the polyacrylamide corresponds to the discharged state of the macroion from hydrolysed polyacrylamides. Similarly, total expansions and expansions attributable to long-range interactions were evaluated using the estimated intrinsic viscosities at the theta temperature of the parent polyacrylamide and the hydrolysed sample, respectively. The electrostatic expansion coefficients are independent of molecular weight and the long-range expansion coefficients are almost independent of the extent of hydrolysis at high charge densities. In the absence of closed expressions predicting the variation of the expansion coefficients with the concentration of ionizable groups, equivalent expressions based on different theories were deduced assuming that i2/Cs is proportional to the concentration of ionizable groups where i is the extent of ionization of the polyelectrolyte and Cs is the concentration of the added salt. The variation of the electrostatic expansion coefficient with the charge density could not be represented according to any of the theories on macroion expansion. However, attributing the total expansion to the presence of electrostatic charges alone, the Fixman and Chien-Ishihara theories allow a good representation of the data. At very low charge densities, the expansions due to long-range interference effects also can be accounted for by the Fixman and Chien-Ishihara theories.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 2443-2449 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The deactivation of the catalytic activity of the BuOTiCl3/AlEt2Cl initiated polymerization of styrene in heptane was found to follow a second-order rate law. The varying slopes in the second-order plots observed with varying catalyst concentrations are due to the heterogeneous nature of these colloidally dispersed catalysts. Site poisoning by reversible adsorption of the AlEtCl2 formed, is proposed as the probable reason for the deactivation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 186 (1985), S. 123-129 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The potentiometric behaviour of poly(methacrylic acid) was examined in water/1,4-dioxane mixtures at 25°C. Conformational transitions were observed in about the same range of apparent ionization in the 1,4-dioxane concentration range 0 to 15 vol.-%. Transitions were not observed in the 1,4-dioxane concentration range 20 to 35% and the corresponding Henderson-Hasselbalch plots were found to be linear. Phase separations were observed to occur beyond 40 vol.-% 1,4-dioxane. The free energy of the conformational transition decreased very rapidly with the initial incorporation of 1,4-dioxane but slowly at higher concentrations. Van der Waals methyl-methyl interactions as the cause of the compact form has been inferred. The large increase in intrinsic viscosity observed for the unneutralized poly(methacrylic acid) in a relatively narrow range of composition of the 1,4-dioxane/water mixtures has been ascribed to a solvent induced conformational transition.
    Additional Material: 4 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. 1117-1132 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of polymerization of styrene in heptane was investigated using butoxytitanium trichloride and triethylaluminium/triisobutylaluminium as cocatalysts. A steady state polymerization after an initial period of declining rates lasting for 20 - 60 min was observed. Both the catalysts systems polymerize styrene at a slow rate ( ≈ 10-6 mol · dm-3 · s-1). The steady state rates show a maximum at an [A1] : [Ti] ratio of 1,5 and exhibit a first-order rate law with reference to both the monomer and the catalyst. Addition of triethylamine, an electron donor, greatly influences the rates of polymerization when triethylaluminium is used, whereas in the case of triisobutylaluminium, the rates are not greatly influenced by the presence or absence of triethylamine. The effect of the electron donor on the rates of polymerization can be explained by the competitive complexation of the alkylaluminium and the electron donor at the active site. The overall activation energy of polymerization (44 - 46 kJ · mol-1) is in accord with a coordinated anionic mechanism. An alkylated alkoxytitanium halide species as the chemical entity affecting polymerization is suggested.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 549-557 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Seven unfractionated samples of polyacrylamide have been investigated in 0,12 M NaCl by viscosity, osmotic pressure, and light scattering techniques. Viscosity-molecular weight and 〈,s2〉w-M̄w relationships have been established and the unperturbed dimensions were estimated from the Stockmayer-Fixman relationship.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 2283-2289 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the polymerization of styrene, using H3C(CH2)3OTiCl3/Al(C2H5)2Cl as catalyst, was examined in a vacuum dilatometer. The polymerization rate was found to decrease continuously with time and the initial and overall rates vary linearly with the catalyst concentration, exhibiting a nearly second-order and first-order dependence, respectively, with regard to the monomer. The decrease of the rate with time is attributed to the chemical deactivation of the sites.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 957-967 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Six unfractionated samples of polyacrylamide were hydrolysed to varying extents. The partially hydrolysed polyacrylamides were investigated by viscosity, osmatic pressure and light scattering techniques in 0,12 M NaCl. The molecular weights of the hydrolysed polyacrylamides confirmed the absence of main chain degradation during hydrolysis. Intrinsic viscosities and dimensions increased with increasing extent of hydrolysis. On correlating the intrinisic viscosities with the extent of hydrolysis, a linear relationship between intrinsic viscosities and the square root of the extent of hydrolysis was obtained.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 983-989 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dimensions of partially hydrolysed polyacrylamides with varying molecular weights and extents of hydrolysis determined by light scattering were used to verify the relative applicability of the various macroion expansion theories. Expansions attributable solely to the presence of electrostatic charges were evaluated with references to the dimensions of the polyacrylamides used for hydrolysis. Total expansions and expansions due to long-range interactions were evaluated with reference to the estimated unperturbed dimensions of the strating polyacrylamides and the hydrolysed polyacrylamide samples, respectively. The expansion coefficients obtained from light scattering measurements were higher than those evaluated from intrinsic viscosities. The differences were maximum (30 - 100%) for the total expansion coefficients. Considering the variation of the Flory viscosity constant Φ with molecular weight and charge density, these differences were ascribed to the uncertainty in the applicability of the light scattering method for the determination of the dimensions of polyelectrolytes. However, the variation of the expansion coefficients with the extent of hydrolysis and molecular weight were similar to those of the expansion coefficients obtained from viscosity measurements. The total expansion coefficient was qualitatively in confirmity with the theory of Chien and Ishihara with reference to its dependence on charge density.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 3 (1982), S. 581-584 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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