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  • Articles: DFG German National Licenses  (11)
  • Chemistry  (11)
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  • Articles: DFG German National Licenses  (11)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 843-856 
    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: As an aid in assessing the ability of antioxidant additives to persist in polymers and thus remain effective in protecting against oxidation, the solubility and diffusion coefficient of two antioxidants in branched polyethylene have been determined in this work. A method was developed for this purpose by which the diffusion coefficient and solubility could be determined simultaneously. The method consists of analyzing the concentration profile across a stack of polyethylene sheets through which the antioxidant was allowed to diffuse. The concentration of antioxidants in polyethylene was determined by a thermogravimetric technique which relies directly on the ability of the additives to suppress oxidation reaction. The diffusion coefficients determined showed excellent agreement with values in the literature which were obtained by a radiotracer method. The solubility of the antioxidants in three normal hydrocarbon solvents of varying molecular sizes was also determined by a conventional technique at various temperatures and found to correlate well with their solubility in polyethylene determined by the diffusion method. In particular, the dependence of the solubility on the size of solvent molecules and on temperature agrees well with an equation derived on the basis of the regular solution theory of liquid mixtures.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 318-322 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Physical aging in polystyrene was studied by annealing samples isothermally (at 22°, 57°, and 93°C) for various lengths of time and measuring the changes in the enthalpy and the flexural creep property. The enthalpy decrease reached a constant value after about 10 hours of aging at 93°C, indicating an apparent attainment of equilibrium, whereas the creep behavior continued to change with prolonged aging even after 10 hours. At room temperature it took about a year of aging to induce a measurable change in enthalpy, while the creep behavior showed changes clearly only after hours of aging. These and other items of evidence indicate that the effect of aging on the creep behavior cannot be interpreted solely in terms of the free volume concept. Thus the hope of being able to predict the mechanical properties of aged polymers from the measurement of specific volume or enthalpy alone is not likely to be realized.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 1103-1109 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: The phase transition and phase separation behavior occurring in mixtures containing an A-B block copolymer and an A homopolymer is discussed. With a pure block copolymer an order-disorder transition can be induced by raising the temperature, whereby the ordered lattice of segregated microdomains becomes unstable and gives way to a homogeneous liquid structure. Small amounts of a homopolymer added to a block copolymer can be accommodated in the microdomains consisting of the same type of monomeric units, up to a solubility limit that depends on the relative lengths of the homopolymer and the copolymer block and on the temperature. The order-disorder transition temperature of the block copolymer is also affected by the added homopolymer. At the other extreme of concentration, spherical micelles of block copolymer are formed when a small amount of the copolymer is added in the bulk homopolymer, and the critical micelle concentration again depends on the relative lengths of the molecules and blocks involved and on the temperature. Measurements were made with light scattering and small-angle X-ray scattering techniques to determine the phase behavior of mixtures containing a styrene-butadiene block copolymer and either a polystyrene or a polybutadiene. The resulting phase diagram exhibits a fascinating complexity. Comparison with recent theories treating these phenomena shows that a good agreement is generally obtained on a qualitative or semi-quantitative level, but a quantitative agreement is often not attained.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 15 (1981), S. 209-230 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The mechanical properties of polyethylene components used in prosthesis are altered after fabrication by the sterilization procedure and by the environmental and mechanical aging which occurs after implantation. To assess the importance and extent of these alterations, ultrahigh molecular weight polyethylenes from two sources, Hercules 1900 and RCH 1000C, were subjected to gamma-ray irradiation and aging in serum and argon environments. Changes induced by these treatments in the structural and mechanical parameters have been determined by a variety of experimental techniques. The effect of irradiation is to introduce crosslinks and to increase the degree of crystallinity resulting in changes in the tensile properties in the direction of higher stiffness and reduced ductility. Aging for six months produced similar changes with subtle differences. The results suggest that the initially low degree of crystallinity which results from the sluggish mobility of the very long chain molecules offers the opportunity for significant changes in the properties during use in the long run.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 27-37 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this, the first of a series of four papers, the theory of diffusion control of the gelation in polyfunctional polyadditions is rejected. It is shown experimentally, that the termination step in a model system is unaffected by diffusion control until after gelation. It is shown theoretically that diffusion control of the crosslinking step sets in even later. Investigations by Grün, and by Vaughan, are relevant to this demonstration. Quantitative application of the Stokes-Einstein theory of diffusion confirms the conclusions reached. In the absence of diffusion-controlled crosslinking, alternative causes are examined for observed delays in gelation. These causes are intramolecular cyclization and chain transfer effects. There are well-known mass law effects of dilution in polyfunctional systems. However, progressive dilution with monovinyl monomer in polyaddition does not - in contrast to the effects of inert diluent in polycondensation - favor internal cyclization. The true mass law effects of such dilution can readily be allowed for.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 57-74 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In a polyfunctional polyaddition system, such as methyl methacrylate/ethylene dimethacrylate (MMA/EDMA), the first elementary reaction step to become affected by diffusion control is the termination step. This is true also in absence of EDMA (pure MMA polymerization), but in the presence of EDMA this diffusion control occurs at much lower conversions. It becomes manifest as the usual Trommsdorf effect (over-all rate acceleration), and begins after the gel point. A general statistical kinetic theory is developed for the Trommsdorf effect. Surprisingly, the theory is more readily applied to crosslinked systems such as MMA/EDMA than to linear systems such as MMA alone. This happens because crosslinking causes useful discontinuities both in the viscosity/time curve and in the size distribution curve of the radicals, whose diffusion behavior determines the Trommsdorf effect. The theory divides these radicals by a size barrier into small radicals which freely diffuse and large radicals which are immobilized. A successful termination step is taken to require at least one mobile radical. To assume that all the radicals are mobile, or that all are immobile, is neither sound in theory nor successful in practice. Theory leads to the conclusion that uncrosslinked radicals should be mobile, while those bearing crosslinks are immobilized beyond the gel point. This conclusion determines the rate curve, and no reasonable amendment will make any difference to the theoretical curve. The curve lends itself to reduction to dimensionless form. Experimental plots are successfully brought to mutual coincidence by this reduction, but not into quantitative coincidence with the theoretical curve. This is attributed to incomplete efficacy of the size barrier, in that even pairs of nominally frozen radicals will occasionally succeed in mutual termination. The theoretical rate curve lies closer to experimental results if radical combination rather than disproportionation is the assumed termination mechanism. The rate theory furnishes an improved explanation of kinks, previously observed in rate curves going through a gel point. The success of the treatment confirms the classical network theory of gelation, and the diffusion control theory of the Trommsdorf effect.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 39-56 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The curve governing the viscosity as a function of conversion in the system methyl methacrylate (95% moles)/ethylene dimethacrylate (5% moles) up to the gel point is predicted theoretically. The classical theory of gelation enters critically into the theory. The excellent experimental verification of the curve thus confirms the applicability of the classical theory and the absence of interference by diffusion control. As the gel point is reached at just over 1% conversion, these experiments require further refinements in the viscodilatometric technique used. The reproducibility during the induction period preceding polymerization of the constant initial volume is attested by a standard deviation of 0.5% calculated on the subsequent shrinkage up to the gel point. The standard deviation of the viscosity during the induction period was 1%. The theory of the viscosity/conversion curve makes a correction for nonideal solution behavior, but this is small here. No allowance is required for chain transfer effects or ring formation within a primary polyaddition chain, which are serious obstacles when at tempting to predict the critical conversion absolutely from the classical theory. Formation of rings involving several primary polyaddition chains is neglected, and this seems justified by the agreement between theory and experiment, and by the statistical theory to be given in the fourth paper of this series. The initial intrinsic viscosity of the system is found to be substantially lower than for pure methyl methacrylate polymerization. This reduction can be formally evaluated in terms of a chain transfer constant to ethylene dimethacrylate monomer. However, the value obtained is too high in comparison with suitable model compounds for this monomer, including ethylene diacetate and difumarate. A large part of the reduction in viscosity is, therefore, attributed to the compacting of the primary chains through formation of internal rings of substantial size.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 75-90 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the model nonlinear polyaddition system methyl methacrylate/ethylene dimethacrylate (MMA/EDMA), the plot of the critical conversion against the rate of polymerization is a straight line. This is in accord with the classical theory of gelation, whose vindication is completed in this paper. To account quantitatively for the slope of the line, internal cyclization within the primary polymerization chains must be extensive. Thus of the order of half the pendent vinyls on such a chain fall to the radical on the same chain, in agreement with theoretical prediction on the basis of molecular models. The intercept of the critical conversion plot at zero rate can also be explained in terms of the internal cyclization reaction, while chain transfer makes at most a small contribution. The dependence of the gel point on the proportion ρ of EDMA unsaturation, over a 250-fold range, is satisfactorily accounted for by the classical gelation theory. A statistical theory of internal cyclization suggests that a steady state is approached in the growth of a given radical chain. Pendent vinyls are then lost by cyclization as fast as they are added by polymerization. The limiting number of pendent vinyls on a primary chain is about 1000 ρ. A statistical theory of multiple crosslinking (cyclization involving more than one primary chain) suggests that it is unimportant. The number of pendent vinyls on a giant molecule grows proportionately to the number of primary chains of which it is comprised. Thus multiple crosslinking has little effect on the classical network theory of gelation, but makes a contribution to the parameter introduced into the theory to correct for internal cyclization. The interplay of kinetic and gelation measurements is useful in mechanistic studies of nonlinear polymerization.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 10 (1972), S. 839-841 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 10 (1972), S. 839-841 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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