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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 331-344 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A quantitative analysis has been made of sorption isotherms and of diffusion data obtained with benzene, acetone, and methanol in ethyl cellulose. The concentration range covered was for volume fractions of penetrant not above 0.1. In this range reproducible measurements were possible. The sorption data show significant departures from the lattice theory of solution. In particular, isotherms tend to curve in the same sense as the Langmuir isotherm; heats of dilution are exothermal; and entropies of dilution are negative. The sign of heats of dilution and the isotherm shapes can be explained if gaps in the polymer provide sorption sites, but the entropy values cannot. An additional ordering or immobilization of the structure around the site, or of penetrant molecules on it, is required. In all these effects it is the nonpolar molecule benzene which shows them most clearly. Diffusion coefficients, D, Arrhenius energies of activation, Ea, and the coefficients D0 in the equation D = D0 exp { -Ea/RT} all depend upon the molecular dimensions of the penetrant. The permeability and D change as the concentration of penetrant increases, except for methanol. These and other aspects of diffusion have been discussed, and compared with results obtained in other polymers.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. 261-275 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The permeabilities and diffusion coefficients of propane, n-butane, and isobutane in stretched peroxide-cured natural rubber have been measured at simple elongations of 0 to 400% in the temperature range 30 to 50°C. To minimize the effect of penetrant on the degree of crystallinity, only regions of low penetrant concentration were chosen. At elongations not sufficient to induce crystallization the permeability did not alter significantly on stretching. At higher elongations the permeability decreased with increasing crystallization. Over a long period of time and at a given temperature the permeability of a crystalline membrane decreased slowly toward an equilibrium value. No such behavior was observed with noncrystalline membranes either stretched or unstretched. Part of the decrease is accounted for by a corresponding slow increase with time in the degree of crystallinity and the remainder is attributed to a partial reorientation or redistribution of the crystallites as the system tends toward an equilibrium state. The data are analyzed in terms of a model in which the crystalline rubber is presented as a rectangular array of small cylindrical crystallites impermeable to penetrant and embedded in an amorphous matrix. To a first approximation the dependence of the permeability on crystallinity and temperature is represented satisfactorily by expressions based on the model. The data indicate that the crystallites may impose slight restrictions on the segmental mobilities in the amorphous regions, but the effect is not pronounced. Some differences between steady and transient state diffusion coefficients are explained in terms of “dead volume” which is present in the steady state of flow to a greater extent than in the transient state.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 315-329 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption and permeation of benzene, acetone, and methanol in and through ethyl cellulose has been investigated from the point of view of hysteresis and time-dependence. The three sorbates are imbibed decreasingly in the order given, at any relative pressure, and so swell the polymer to different extents. The medium is one in which anomalous diffusion is to be expected. The study was made in the lower range of concentrations of penetrant. The initial isotherm of acetone at 50°C. lay below subsequent ones at the same temperature. The higher the temperature the smaller this difference tended to be, while the greater the pressure and so the amount imbibed the greater it became. Eventually “settled” reproducible isotherms were found. If the outgassed polymer, following lower temperature isotherms, was “annealed” at a higher temperature and then cooled again, the initial isotherm at 50°C. was more nearly approached. However, subsequent isotherm determinations at the same temperature again established the “settled” isotherm. Permeation rates were determined as a function of pressure under various treatments. Repeated permeation runs caused the permeability of the polymer to decrease to a “settled” value. This behavior may be ascribed to some orientation of polymer, by mass flow, during permeation. After establishing the settled permeability the polymer was outgassed and “annealed” at a higher temperature, and the permeability at the original temperature then lay below the “settled” value. Benzene, which swelled the membrane more than the other sorbates, showed more pronounced effects of the same kind as acetone. On the other hand methanol, which was least sorbed, showed less pronounced time- and history-dependence. Sorption always occurred more slowly than desorption. The various effects have been discussed in terms of a model of the polymer having rather stiff chains with some semipermanent interchain bonds, but other bonds more easily rearranged. The history-dependent effects can arise at temperatures well above the glass transition usually quoted for ethyl cellulose.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 377-386 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An account has been given of sorption and diffusion of water by ethyl cellulose. In contrast with diffusion coefficients of some other penetrants, those of water decrease with increase of water sorption in the manner previously observed by Rouse for water-polythene systems. The sorption isotherms have the opposite curvature to Langmuir or Freundlich isotherms, and hence also to the isotherms of benzene, C4 and C5 paraffins, or acetone sorbed at low penetrant concentration by the same polymer. The results have been interpreted in terms of cluster formation of water molecules either in preexisting cavities in the polymer or, less probably, in the polymer matrix itself. Visual evidence of cluster formation is provided by the onset of light scattering by the membrane as the relative humidity reaches a critical range. The opacity disappears again as the humidity is decreased.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 15 (1977), S. 565-576 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 2005-2017 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Styrene has been polymerized thermally at 60.5°C, without added initiator, in the presence of ferrocene. An increase in the rate of polymerization was observed, but the degree of polymerization remained constant. Evidence of ferrocene-styrene interaction is presented, and a kinetic scheme involving propagation with styrene in such an interaction state is proposed to account for these findings. Various kinetic parameters defined by this scheme have been evaluated.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 2133-2141 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the AIBN-initiated homopolymerization of vinylferrocene in dioxane has been investigated at 60°C. The rate of polymerization was found to be dependent on the monomer concentration to a power 0.97 and on the initiator concentration to a power 0.42. The overall activation energy for polymerization over the range 50-80°C was 84 kJ/mole. Analysis of polymer molecular weight data gave the chain transfer constant to monomer Cm as 1.2 × 10-2 and analysis of both rate and molecular weight data gave kp/(kt)0.5 as 2.36 × 10-2 dm1.5/mole0.5-sec0.5. Mössbauer and ESR spectra indicated the absence of Fe(III)-containing paramagnetic species in the polyvinylferrocene formed under these conditions.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 2621-2633 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Styrene has been polymerized thermally at 60°C in the presence of low concentrations of vinylferrocene and in the presence and absence of 2,2′-azobisisobutyronitrile (AIBN). The polymerizations were studied in bulk and also in benzene solution. The thermal polymerization of styrene in the presence of ethylferrocene, but without added AIBN or solvent, was also examined. The bulk polymerizations exhibited high initial rates of polymerization followed by a decrease in rate. Initial rates of polymerization for bulk polymerizations in the absence of AIBN have been interpreted by means of a kinetic scheme involving propagation with styrene participating in a specific interaction with the ferrocene derivative and some kinetic parameters associated with this scheme have been evaluated. The decrease in the rate of polymerization is due to the formation of a retarder. The benzene solution polymerizations fitted a simple kinetic scheme and the transfer constant for vinylferrocene with respect to polystyryl radicals Cs, has been evaluated as 1.98 × 10-3.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 533-537 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nylon 66 [poly(hexamethylene adipamide)] and Nomex [poly(m-phenylene isophthalamide)] were metalated by using solutions of sodium in liquid ammonia. Metalation of the Nomex polymer was also carried out by using sodium naphthalene in tetrahydrofuran. The metalated polymers were then reacted with acrylonitrile monomer to yield the corresponding anionic graft copolymers. The heterogeneous nature of these reactions is discussed in relation to the structure of the graft copolymers.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 2879-2885 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relatively high-molecular-weight segmented polyurethanes based on methylene bis(4-phenyl-iso-cyanate), poly(propylene glycol), butane-1,4 diol, and cis-2-butene-1,4 diol have been synthesized and characterized. These unsaturated polyurethanes were successfully grafted using N-vinyl pyrrolidone as monomer and 2,2′-azobisisobutyronitrile as free-radical initiator. However, grafting experiments involving benzoyl peroxide as initiator were unsuccessful. The graft copolymers were isolated from the ungrafted polyurethane and poly(N-vinyl pyrrolidone) by selective solvent extraction. Elemental microanalysis, IR, NMR, thermogravimetric analysis, and equilibrium water sorption measurements were used to characterize the graft copolymers.
    Additional Material: 3 Ill.
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