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  • Polymer and Materials Science  (962)
  • 1970-1974  (962)
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Year
  • 1
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 65-79 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the isomorphous relationships existing among five crystalline polyaromatic polymers containing O, S, CH2 bridges, i.e., where Ph is phenyl, is reported. Appropriate series of oligomers corresponding to these polymers have also been prepared in order to investigate how the solid-state properties of the oligomers correlate with those of the polymers. A preliminary x-ray analysis is reported showing that the polymers are actually isostructural.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 1759-1764 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 3255-3269 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical-induced grafting of styrene onto polybutadiene (PBD) in benzene solution at 60°C has been studied. Provided the PBD concentration is kept below about 1.0 monomermole/l. the polymerization of styrene shows normal kinetic behavior. The proportion of polystyrene incorporated as graft is independent of the initiator (benzoyl peroxide) concentration but increases as the ratio of PBD to styrene in the reaction medium increases. Azobisisobutyronitrile produces no graft copolymer in this system. It appears that the reaction leading to graft formation is direct attack of initiator radicals on the rubber, probably by a hydrogen-abstraction reaction.
    Additional Material: 18 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1011-1021 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic analysis of the grafting reaction has shown that, provided rubber radicals are not involved in termination reactions, the observed normal kinetics of styrene polymerization are to be expected. An expression relating the graft fraction with the rubber and monomer concentrations has been derived and its validity verified from the results reported in Part I. The observation that the molecular weight of the ungrafted PBD falls during the reaction has been explained on a theoretical basis.
    Additional Material: 2 Ill.
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  • 6
    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 dynamic-mechanical properties as a function of temperature and the low- and high-speed tensile properties at 23°C have been determined on specimens of conventional suspension-polymerized PVC and of low-temperature-polymerized PVC roll milled and then compression molded at different temperatures. It has been found that the main transition α and the shear modulus above Tα depend on the thermal history and are strongly affected by crystallinity, whereas the dynamic-mechanical spectrum below Tα is not influenced by these parameters. Room-temperature tensile modulus and yield properties are very little affected by processing history and crystallinity. The elongation at break and the fracture energy, on the contrary, increase, at any fixed strain rate, for conventional PVC with milling temperature. The same trend has been found for low-temperature PVC, but the elongation at break-versus-temperature curve is shifted, as a whole, toward higher temperatures by approximately 50°C. Such results are discussed in terms of homogeneity of the specimens, which is controlled by the melting process of the crystallites. Stereoscanning electron micrographs of fracture surfaces appear to substantiate these conclusions.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 139 (1970), S. 115-138 
    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: The macroscopic melting temperatures of oligomer chain molecule crystals depend uniquely on the shape and size of the crystals and the chain conformation of the molecule in the melt. The morphology of the crystals as well as the conformation in the melt are influenced by the specific chemical structure of these molecules. This is quantitatively discussed on the basis of simplifying models of single component systems of n-paraffine, mono- and dicarboxylic acids and two oligomers of the nylon type. In systems which crystallize completely and in extended chain morphologies the melting temperatures can be calculated as a function of the chain length for the different types of oligomers with the same thermodynamical treatment considering only the different conformation of the specific oligomers in the melt. Single component systems with one specified endgroup cannot crystallize completely. These partially crystalline systems can be described in terms of the equilibrium thermodynamics in which additional phenomenological parameters are included reflecting the noncrystalline fraction of the enthalpy of the sample, and the entropy content of the “amorphous” longitudinal border regions of the extended chain crystal.
    Notes: Die makroskopisch meßbare Schmelztemperatur von Kettenkristallen aus oligomeren Ketten hängt definiert von der Gestalt und Größe der Kristalle sowie von der Konformationsfähigkeit der Ketten in der Schmelze ab. Die Morphologie der Kristalle ebenso wie die Konformationsmöglichkeiten der Ketten in der Schmelze werden ihrerseits wesentlich durch die spezielle chemische Struktur der Kettenmoleküle mitbestimmt. Derartige Zusammenhänge werden für homologe Reihen oligomerer Einstoffsysteme der n-Paraffine, der Mono- und Dicarbonsäuren sowie zweier Oligomerer des Nylontyps diskutiert. In Systemen, die vollständig kristallisieren und die allein Kettenkristalle ausbilden (keine Molekülfaltung), kßnnen die Schmelztemperaturen abhängig von der Kettenlänge für verschiedene Oligomer-Typen mit demselben thermodynamischen Formalismus berechnet werden, wenn man nur zusätzlich bestimmte Konformationsmöglichkeiten des Oligomeren in der Schmelze berücksichtigt. Schmelztemperaturen partiell kristallisierter Oligomer-Systeme können thermodynamisch auch beschrieben werden, wenn man geeignete innere Zusatzparameter einführt. Diese Zusatzparameter können in qualitative Beziehung zu Eigenschaften des Molekülbaues gebracht werden.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1061-1084 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic shear modulus and the flow rate through capillaries under constant pressure and under constant velocity of the piston, have been measured for polybutadienes and polyisoprenes of narrow molecular weight distribution with molecular weights ranging, respectively, from 3.8 × 104 to 5.8 × 105 and from 1.06 × 105 to 6.02 × 105. The phenomena of the discontinuous increase of volume flow rate and self-oscillatory flow regime at critical rates of deformation have been considered in detail. It is proposed that these phenomena are due to the induced transition of the polymer from the fluid to the high-elastic state at higher deformation rates. As a result, an inference has been made that polybutadienes and polyisoprenes with a narrow molecular weight distribution in the high-elastic state, behave in certain respects as crosslinked polymers incapable of displaying fluidity. The quantitative relationships among the viscoelastic characteristics measured under dynamic regimes, the parameters determining the critical flow regimes, and the molecular weights of polybutadienes and polyisoprenes have been worked out.
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 6 (1972), S. 59-79 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Advantages of a hollow-fiber hemodialyzer have been well described. The goal of this program was to provide a working model of a noncellulosic hollow fiber artificial kidney with nonthrombogenic blood-contacting surfaces, low blood-priming volume and low pressure drop, a satisfactory rate of urea transport, and high rate of ultrafiltration of water. Also, the reliability and utility of these devices was to be demonstrated through clinical evaluation.
    Additional Material: 9 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 3455-3460 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crosslinking in the styrene-butadiene emulsion copolymerization (21 parts styrene:79 parts butadiene) prior to gelation has been studied by means of partial conversion number-average molecular weights at 5, 15, and 25°C. It is shown that the macromolecular population begins to diminish at progressively lower conversions as the reaction temperature is increased. This is attributed to the relative increase in crosslinking over propagation as the reaction temperature is increased and also to the decrease in mercaptan regulating index with increasing temperature.
    Additional Material: 6 Ill.
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