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  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly[sulfadiazinacrylamid] (5) mit 14C-Hauptkettenmarkierung wurde synthetisiert und sein Molekulargewicht viskosimetrisch durch Vergleich mit inaktiven Proben von Poly-[sulfadiazinacrylamid] mit membranosmometrisch ermittelten Molekulargewichten ähnlicher Größe bestimmt.In seinem systemischen Verhalten bei Mäusen zeigte die Verbindung einen polymerspezifisch protahierten Verlauf. Die Ausscheidungsraten des Polymeren waren vernachlässigbar gering, seine Toxizität erheblich. Es wurde im Untersuchungszeitraum in der Leber akkumuliert, aber eine Tumoraffinität zum PC6 Plasmazelltumor bei Mäusen war nicht feststellbar.
    Notes: Poly[sulfadiazineacrylamide] (5), labeled with 14C in the main chain, was synthesized and its molecular weight viscosimetrically determined by comparison with unlabeled samples of poly[sulfadiazineacrylamide] with similar molecular weights which were determined by membrane osmometry.The material showed a polymer-specific prolongation of its systemic behaviour in mice. Rates of excretion of the polymer were negligibly low, whereas the toxicity was considerable. It was concentrated in the liver during the course of the experiment, but no affinity toward the PC6 plasmacytoma in mice could be detected.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 201-214 
    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: The diffusivities of simple gases through a series of polyurethane block copolymers of differing aromatic urethane content and type of soft segment were measured using a quadrapole mass spectrometer as a detecting device. Although an Arrhenius expression generally described the temperature dependence of diffusion in this system, a discontinuity was observed in the Arrhenius plots for some materials, and the discontinuity was found to be related to the onset of the glass transition in the hard domains. Increasing the hard segment content of the materials decreased the diffusivity due to the increase in the activation energy of diffusion. Increasing the soft segment length brought about a decrease in the activation energy with an increase in diffusivity. Polyster urethanes had lower activation energies for diffusion than polyether urethanes of similar hard segment composition. Finally, as the penetrant diameter was increased, a decrease in the diffusivity and an increase in the activation energy was noted.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1040-0397
    Keywords: Glucose ; Biosensor ; Nafion ; Oxygen dependence ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have prepared amperometric glucose sensitive electrodes with a composite active layer consisting of Nafion, glucose oxidase, and carbon-supported platinum particles. A particularly advantageous configuration results from the use of such a film on a gas diffusion electrode. We demonstrate that the gas diffusion electrode configuration enables us to supply oxygen from the back of the electrode, thus providing the capability of operating the sensor independent of dissolved oxygen. The insensitivity to solution oxygen concentration has been demonstrated by monitoring the glucose response of the electrode after extensive deoxygenation of solution. Cast composite layers yield mechanically robust coatings with high enzyme loadings, and thus high sensitivity to glucose. The electrode responds rapidly and is stable over a long period (90% activity after more than half a year) when stored in solution. We have optimized the composition of the sensitive layer with respect to Nafion to C/Pt ratio and enzyme loading.
    Additional Material: 7 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 1 (1959), S. 107-113 
    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: A theoretical treatment is given which predicts the behavior of a foamed elastic material on the basis of a model consisting of a network of thin threads. Two cases are considered: (1) small strains, and (2) finite compressions, when the major part of the deformation of the threads is attributed to buckling. The behavior is given in terms of Young's modulus of the matrix and the density of the foam. Measurements of the load-deformation relations for small tensile strains and finite compressions are described for natural rubber foams prepared from latex. A wide range of density is covered (0.09-0.57), giving a variation of compression hardness of about 100:1. Satisfactory agreement with theory is found for both the cases considered, indicating that the basic concepts of the structure and mode of deformation are correct.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 354-357 
    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: A theoretical treatment is given which predicts the tear strength of a foamed elastic material. The energy required to break a test-piece in simple extension is also calculated, on the assumption that tensile failure occurs by catastrophic tearing from a small nick of a similar size to the largest pore present in the test-piece. The behavior is given in terms of the strength of the matrix, the density of the foam, and the pore size. Measurements of the tear strength, tensile strength, and elongation at break are described for natural rubber foams prepared from latex. A wide range of density is covered (0.09-0.5) giving a variation in tear strength of 9 : 1 and in work-to-break of 24 : 1. Satisfactory agreement with theory is found in both cases, indicating that the basic concepts of the modes of failure are correct. It is concluded that uniformity of pore size is required for maximum strength, and a large average pore size for high tear resistance.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 4 (1995), S. 111-117 
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When randomly branched polymers are grafted to a surface, polymer brushes are the result, similarly as well known in the case of linear grafted polymer chains. These brushes behave, however, special, as severe restrictions in the conformation of individual polymers are present. These restrictions are firstly due to the high degree of branching and secondly to the natural maximum stretching ratio of the branched molecules, that is given by Hmax = aM1/D. a is the typical size of a monomeric unit, D is the spectral dimension and M the total mass of the branched polymer. Brushes cannot exceed this height, and limits on the grafting density as functions of the spectral dimension are investigated. For all thermodynamic situations the minimum area per chain scales as σmin = aM(D - 1)/D.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 7 (1998), S. 59-63 
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this note microgels with and without excluded volume interactions are considered. Based on earlier exact computations on Gaussian mircogels, which are formed by self-crosslinking (with M crosslinks) of polymer chains with chainlength N, Flory type approximations are used to get first insight to their behavior in solution. It is shown that two different types of microgels exist: A special type of branched polymer whose size scales as R ∝ N2/5/M-1/5, instead of R ∝ N1/2. The second type are c*-microgels whose average mesh sizes r are swollen and form self avoiding walks with a scaling law of the form r = a(N/M)3/5.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 7 (1998), S. 241-247 
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A self-consistent field (SCF) theory for the adsorption of polyelectrolyte chains onto oppositely charged spheres is considered. It is demonstrated that the criterion for critical adsorption shows a different behavior for small and large curvature of the surface. Experiments give indeed evidence for the power-law behavior as theoretically predicted for large curvature.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 5 (1996), S. 573-643 
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymer systems are discussed in the framework of the Landau-Ginzburg model. The model is derived from the mesoscopic Edwards Hamiltonian via the conditional partition function. We discuss flexible, semiflexible and rigid polymers. The following systems are studied: polymer blends, flexible diblock and multi-block copolymer melts, random copolymer melts, ring polymers, rigid-flexible diblock copolymer melts, mixtures of copolymers and homopolymers and mixtures of liquid crystalline polymers. Three methods are used to study the systems: mean-field model, self consistent one-loop approximation and self consistent field theory. The following problems are studied and discussed: the phase diagrams, scattering intensities and correlation functions, single chain statistics and behavior of single chains close to critical points, fluctuations induced shift of phase boundaries. In particular we shall discuss shrinking of the polymer chains close to the critical point in polymer blends, size of the Ginzburg region in polymer blends and shift of the critical temperature. In the rigid-flexible diblock copolymers we shall discuss the density nematic order parameter correlation function. The correlation functions in this system are found to oscillate with the characteristic period equal to the length of the rigid part of the diblock copolymer. The density and nematic order parameter measured along the given direction are anticorrelated. In the flexible diblock copolymer system we shall discuss various phases including the double diamond and gyroid structures. The single chain statistics in the disordered phase of a flexible diblock copolymer system is shown to deviate from the Gaussian statistics due to fluctuations. In the one loop approximation one shows that the diblock copolymer chain is stretched in the point where two incompatible blocks meet but also that each block shrinks close to the microphase separation transition. The stretching outweights shrinking and the net result is the increase of the radius of gyration above the Gaussian value. Certain properties of homopolymer/copolymer systems are discussed. Diblock copolymers solubilize two incompatible homopolymers by forming a monolayer interface between them. The interface has a positive saddle splay modulus which means that the interfaces in the disordered phase should be characterized by a negative Gaussian curvature. We also show that in such a mixture the Lifshitz tricritical point is encountered. The properties of this unusual point are presented. The Lifshitz, equimaxima and disorder lines are shown to provide a useful tool for studying local ordering in polymer mixtures. In the liquid crystalline mixtures the isotropic nematic phase transition is discussed. We concentrate on static, equilibrium properties of the polymer systems.
    Additional Material: 28 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2617-2628 
    ISSN: 0887-6266
    Keywords: dibenzylidene sorbitol ; polymer crystal nucleation ; polypropylene ; clarifying agent ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Recent studies have demonstrated that addition of a small quantity of dibenzylidene sorbitol (DBS) to a molten polymer may result in a physical gel if conditions permit the DBS molecules to self-organize into a three-dimensional network composed of highly connected nanofibrils. If the polymer crystallizes, DBS may also serve as a nucleating agent, promoting the formation of spherulites, especially in commercially important polyolefins such as polypropylene. We examine the thermal and mechanical properties, as well as the morphological characteristics, of an isotactic polypropylene copolymer with 3 wt % ethylene upon addition of less than 1 wt % of 1,3:2,4-di-p-methylbenzylidene sorbitol (MDBS). From dynamic rheological measurements, pronounced complex viscosity increases, attributed to MDBS nanofibril network formation, are observed at concentration-dependent temperatures above the melting point of the nucleated copolymer. Transmission electron micrographs of RuO4-stained sections confirm the existence of MDBS nanofibrils measuring on the order of 10 nm in diameter and, at higher concentrations, fibrillar bundles measuring up to about 200 nm across and several microns in length. The addition of MDBS at different concentrations is also found to promote increases in optical clarity, yield strength, tensile strength, and ultimate elongation of modified copolymer formulations. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2617-2628, 1997
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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