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  • Polymer and Materials Science  (284)
  • FLUID MECHANICS AND HEAT TRANSFER  (63)
  • Inorganic Chemistry
  • 1985-1989  (380)
  • 1980-1984
  • 1925-1929
  • 1988  (380)
Collection
Keywords
Publisher
Years
  • 1985-1989  (380)
  • 1980-1984
  • 1925-1929
Year
  • 1
    Electronic Resource
    Electronic Resource
    Crystallinities of copolymers of ethylene and 1-alkenes (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1271-1286 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Random copolymers of ethylene with 1-butene, 1-octene, and 1-octadecene have been prepared using a homogeneous vanadium-based catalyst system. Comonomer contents determined by 13C-NMR analysis of polymer solutions are in the range 1-10 mol%. Crystallinities were estimated by means of density measurements, x-ray diffraction, differential scanning calorimetry, laser Raman spectroscopy, and CPMAS 13C-NMR spectroscopy. The results are compared with those obtained for heterogeneous copolymers of ethylene containing 1-4 mol% 1-butene. As the comonomer content is increased, the crystallinity decreases. The dimension perpendicular to the 110 plane in orthorhombic crystallites decreases linearly with crystallinity. This decrease in crystallite size is accompanied by an increase in the size of the orthorhombic unit cell. For copolymers containing large amounts of 1-octene and 1-octadecene, a second crystalline form appears. Differences in estimates of crystallinity are discussed in terms of looser packing in highly branched copolymers and the extent to which the second crystalline form participates in the phase structure.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1988.090260611
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  • 2
    Electronic Resource
    Electronic Resource
    Thermal behavior of cast polyurethane elastomers (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1803-1815 
    Details
    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: Thermal properties like glass transition temperature (Tg), initial decomposition temperature (idt), integral procedural decomposition temperature (ipdt), and temperature at various % weight loss of a number of polyurethane systems are reported in this paper. Glass transition temperature was determined on TMA, and other thermal properties were determined by thermogravimetry. The experiments were designed to understand various factors such as length of chain extender moiety, flexibility of chain extender units by substitution of ether link in the diol chain, nature of bonds (unsaturation) in the extender unit, and nature of diisocyanates.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070350708
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  • 3
    Electronic Resource
    Electronic Resource
    Consistent values of rate parameters in free radical polymerization systems (1988)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 293-297 
    Details
    ISSN: 0887-6258
    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
    URL: http://dx.doi.org/10.1002/pol.1988.140260704
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  • 4
    Electronic Resource
    Electronic Resource
    Polymer compatibility and interpolymer association in the poly(acrylic acid)-polyacrylamide-water ternary system (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 707-716 
    Details
    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: Polyacrylamide and poly(acrylic acid) form a water-insoluble phase when solutions of the two having concentrations that are not too low are mixed. The insoluble complex contains nearly stoichiometric 1 : 1 ratios of acrylamide and acrylic acid. The phase behavior of the ternary system was studied as a function of the degree of neutralization, α, of poly(acrylic acid). The complex is not formed when α is high. The formation of the complex was studied by measurement of pH increases observed when poly(acrylic acid) was titrated with polyacrylamide to infer a degree of linkage, θ, between the two polymers. A Hill plot of the data showed that the association was cooperative when the molecular weight was high.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070350311
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  • 5
    Electronic Resource
    Electronic Resource
    Thermal degradation of poly(aryl-ether-ether-ketone) (PEEK): A differential scanning calorimetry studyIssued as NRCC No. 28274. (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 1097-1106 
    Details
    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: Differential scanning calorimetry (DSC) has been used to study the crystallization kinetics and thermal characteristics of poly(aryl-ether-ether-ketone) (PEEK) samples heated under a variety of conditions. Samples were heated in nitrogen and air at temperatures between 380 and 420°C for times up to 120 min. The results indicate that as the holding time and temperature of the melt increased, the amount of recrystallizable material decreased, especially when heated in air. Isothermal crystallization kinetics confirmed the presence of a two-stage crystal nucleation and growth process with Avrami exponents of the order of about 2.4 and 1.5 for the first and second processes, respectively. Analysis of the primary crystallization process using the Avrami equation revealed that PEEK samples heated above the melt temperature in air crystallized at a much slower rate than samples heated in nitrogen.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070360510
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  • 6
    Electronic Resource
    Electronic Resource
    Molecular orbital analysis of the XPS spectrum of a fluorine containing polyimide: PMDA-BDAF (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1199-1205 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results of XPS measurements and molecular orbital calculations performed on the fluorine containing polyimide, PMDA-BDAF, are presented. The calculated carbon 1s (C1s) core energy level positions are compared with the level positions inferred from the XPS measurements. Within Koopman's approximation, the observed shape of the main XPS peak is consistent with the calculated distribution of C1s levels under this peak. Comparison of the magnitude of the carbonyl XPS peak intensity with the main peak intensity indicates a carbonyl C1s signal deficiency compared with that expected for “ideal bulk stoichiometry” i.e., for a polymer with no crosslinks or chain terminations. Comparison of data obtained from a grazing emission (surface sensitive) geometry with that obtained from a normal emission geometry, which probes more deeply into the bulk, indicates a signal enhancement of the C1s levels associated with carbon atoms of the CF3 groups as one nears the polymer surface. Such enhancement might be due to either actual differences in chemical composition, or to preferential structural ordering near the polymer surface.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1988.080260420
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  • 7
    Electronic Resource
    Electronic Resource
    Radiation-induced copolymerization of hydrophilic monomers: Synthesis and thermal properties (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 445-455 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced bulk copolymerization of 2-hydroxyethyl methacrylate (HEMA), 2-hydroxypropyl methacrylate (HPMA), and N-vinyl-2-pyrrolidone (NVP) with methacrylic acid (MAA) was studied by using 60Co γ-radiation at a dose rate of 0.16 ± 0.02 M rads/h. The copolymer composition was estimated from the carboxylic acid content and the reactivity ratios were determined by Kelen-Tüdós. In all the systems MAA was found to be the most reactive. The copolymers were characterized by intrinsic viscosity measurements in dimethyl formamide (DMF) at 30 ± 0.1°C. The thermal behavior of the copolymers was evaluated.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1988.080260209
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  • 8
    Electronic Resource
    Electronic Resource
    Photophysics of polymer-bound 2-(2′-hydroxyphenyl)-2H-benzotriazole photostabilizers (1988)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 505-510 
    Details
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1988.140261203
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  • 9
    Electronic Resource
    Electronic Resource
    Effects of ionizing radiation on epoxy, graphite fiber and epoxy/graphite fiber composites. Part I: Surface energy changes (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 245-255 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Surface energy changes of an epoxy based on tetraglycidyl diaminodiphenyl methane (TGDDM)/diaminodiphenyl sulfone (DDS), T-300 graphite fiber, and T-300/5208 (graphite fiber/epoxy) composites have been investigated after irradiation with 0.5 MeV electrons. The surface energy of TGDDM-DDS epoxy increases monotonically with radiation doses up to 1,000 Mrad mainly due to increased concentration of polar groups. IR and ESCA spectral evidence indicates that carbonyl groups are formed, probably from the tertiary hydrogen at the carbon where the —OH group is attached in the cured epoxy. The polarity of the graphite fiber and the graphite fiber/epoxy interface also increases with radiation dose. These results and the roles of oxygen are discussed in connection with mechanical properties of epoxy/graphite fiber composites exposed to ionizing radiation.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1988.090260203
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  • 10
    Electronic Resource
    Electronic Resource
    Effect of ionizing radiation on the dynamic mechanical properties of an epoxy and a graphite fiber/epoxy composite (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 2029-2042 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: TGDDM/DDS epoxy and T300/NARMCO 5208 composite specimens were exposed to 0.5 MeV electrons to dose levels up to 10,000 Mrad, and the effects of radiation on the mechanical properties were characterized using dynamic mechanical analysis (DMA). In nominally cured specimens there remain unreacted epoxide groups because the epoxy system vitrifies during the cure, preventing additional reaction. DMA shows that ionizing radiation continues the reactions of epoxide groups. Also, the ultimate glass transition is shown to decrease monotonically with radiation dose. The room temperature elastic modulus of the epoxy increases slightly with radiation, but at temperatures exceeding 100°C there is a slight decrease with radiation. There is a dynamic loss phenomena associated with the composites, not seen in the epoxy, that is thought to be due to the interphase region between the fiber and the matrix.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1988.090261002
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