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  • Chemistry  (60)
  • Physics  (20)
  • Wiley-Blackwell  (80)
  • American Chemical Society (ACS)
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  • Oxford University Press
  • 2010-2014
  • 1980-1984  (59)
  • 1965-1969  (21)
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  • Wiley-Blackwell  (80)
  • American Chemical Society (ACS)
  • American Institute of Physics (AIP)
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  • 11
    Electronic Resource
    Electronic Resource
    Solid state extrusion of ultra high molecular weight polyethylene. Processing and properties (1980)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 555-561 
    Details
    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 techniques of solid state coextrusion and powder extrusion have been employed for the deformation of ultra high molecular weight polyethylene. Chain folded and chain extended morphologies obtained under different crystallization conditions were coextruded within a nylon 11 casing acting as a processing aid at an extrusion draw ratio (EDR) of 5 at ≤ 120°C and 0.20 GPa. The powder was compacted and extruded at ≤ 128°C and 0.23 GPa up to an EDR of 24. The physical and mechanical properties of the extrudates were evaluated and found to be dependent on intial morphology. An extrudate from the chain-folded morphology gave a low modulus of 0.71 GPa, the chain-extended morphology a modulus of 6.7 GPa, and the compacted powder a modulus of 15 GPa.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760200808
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  • 12
    Electronic Resource
    Electronic Resource
    13C NMR characterization of intermolecular interactions for polymers. Part 3. Solvent effect on the blend compatibility of poly(vinyl methyl ether) and polystyrene (1982)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 1109-1116 
    Details
    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 solvent has an influence on the homogeneity of the poly(vinyl methyl ether)-polystyrene, PVME-PS blends Prepared by drying cosolutions. This influence has been analyzed in terms of the competition among polymer-polymer and polymer-solvent interactions. Model solutions have been prepared in which intermoleeular interactions correspond to the interactions in this blend and in some of the cosolutions. These interactions in the model solutions have been detected and identified by applying Rummens' method. The 13C NMR spectra have been determined for PVME and for styrene oligomer dissolved in n-alkanes, cyclohexane, diethyl ether, isopropyl methyl ether, diisopropyl ether, and chloroform, and for PVME dissolved in benzene, toluene, and cumene. The chemical shifts have been plotted against the parameter g2 = [(n22 - 1)/(n22 + 1)]2, where n2 is the refractive index of the solvent. If the structural segment represented by certain carbon and some solvent has an interaction that is stronger than dispersive, the chemical shift for this carbon will deviate from the line formed by its shifts in n-alkane solutions, these deviations indicate characters and intensities of the intermoleeular interactions. Results indicate that cyclohexane exhibits weak interactions with both of the polymers and does not interfere with their mutual interaction, leading to a compatible blend. Results also suggest that benzene and toluene interact in the PVME in the same manner as PS. This leads to a gradual increase of the number of polymer-polymer interactions as the concentration of the polymers is increased by solvent removal, resulting in a compatible blend. Chloroform apparently interacts more strongly with PVME than with PS but interacts strongly enough with both to restrict interaction among the two polymers. As the concentration of polymers in the cosolution is increased, PS forms a separate phase. This leads to an inhomogeneous blend when the solvent is evaporated.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760221710
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  • 13
    Electronic Resource
    Electronic Resource
    A rheological interpretation of torque-rheometer data (1967)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 7 (1967), S. 45-51 
    Details
    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
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760070112
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  • 14
    Electronic Resource
    Electronic Resource
    Microhardness of extruded high density polyethylene fibers (1980)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 393-395 
    Details
    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: High-density polyethylene of high tensile modulus has been produced by solid state extrusion using an Instron capillary rheometer. Microhardness measurements on these ultraoriented fibers have been made to assess their perfection from values of the tensile elastic modulus and shear strength. The microhardness tests were measured using a Vickers square diamond. The microhardness increased with the common temperature for crystallization and extrusion, likely due to improvement in the lateral packing of microfibrils. The variation of microhardness with draw ratio is also illustrated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760200603
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  • 15
    Electronic Resource
    Electronic Resource
    A study of the structural integrity of graphite composite structure subjected to low velocity impactPresented at the 35th Annual Technical Conference, 1980 Reinforced Plastics/Composites Institute, the Society of the Plastics Industry, Inc. (1981)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 493-498 
    Details
    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: An analysis for the transient deflections, bending strains, and interlaminar shear stresses in a simply supported laminated composite plate subject to low velocity impact has been obtained using a series solution of the plate governing equations. Results are presented showing the effect of plate geometry and impact location on damage mode. Computed stresses and strain are compared with impact test data to verify, the analysis.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760210809
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  • 16
    Electronic Resource
    Electronic Resource
    NMR characterization of intermolecular interactions for polymers, IV. Intermolecular interactions of low molecular weight analogues for compatible blends of polystyrene and poly(2,6-dimethyl-1,4-phenylene oxide) (1983)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 650-657 
    Details
    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 intermolecular interaction, IMI, leading to the compatibility of polystyrene, PS, and poly (2,6-dimethyl-1,4-phenylene oxide), PPO, has been identified by analyzing the IMI of the model compounds of low molecular weight; cumene, styrene oligomer, 2,6-dimethyl phenol, and its trimer. The IMI has been detected and identified applying Rummens' method for the analysis of the solvent-induced changes in NMR chemical shifts. The results indicate that the driving force in the formation of the compatible blend of PS and PPO is the π-hydrogen bond between the electrodeficient methyl groups in PPO and π-orbitals in PS. There were no indications that n-hydrogen bonds are formed between ring hydrogens of PS and the oxygen in PPO.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760231203
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  • 17
    Electronic Resource
    Electronic Resource
    Annealing of ultra-oriented high density polyethylene extrudates (1983)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 521-529 
    Details
    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 annealing characteristics of highly-oriented, high density polyethylene (HDPE) fibers extruded at 90°C to constant extrusion draw ratios (EDR) of 5.8 to 30 have been studied using small-(SAXS) and wide-angle (WAXD) x-ray diffraction, differential scanning calorimetry (DSC), thermal shrinkage and tensile tests. The thermal stability in macroscopic properties, such as transparency, sample dimension, and tensile modulus, remarkably increases with the sample EDR. However, the folded chain crystals within microfibrils sensitively reorganize on annealing at ≥ 110°C, even when the macroscopic properties exhibit no significant changes at high EDR's. Although the EDR has a minor effect on the reorganizability of the fold chain crystals, it has a major influence on the SAXS intensity and the extended chain crystalline component detected by WAXD for both unannealed and annealed extrudates. This specific crystalline component has an improved thermal stability and enhances the thermal stability of macroscopic properties at higher EDR. The fibers extruded at 90°C in this study and those prepared at 134°C in a prior study, exhibit significantly different melting behavior after annealing and for long period vs. EDR relationships. These facts combined with the independent observations of the effect of annealing and extrusion temperatures on the consequent long period strongly suggest that annealing during extrusion plays an important role in determining the microstructure of extrudates, especially for extrusion near the ambient melting point of the polymer.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760230908
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  • 18
    Electronic Resource
    Electronic Resource
    Absorption of NH3 by nylon-6 (1982)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 519-520 
    Details
    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
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760220811
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  • 19
    Electronic Resource
    Electronic Resource
    Interfacial polymerization of n-alkyl α-cyanoacrylate homologs (1966)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1617-1623 
    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: The n-alkyl α-cyanoacrylates from methyl through n-octyl exhibit a reverse order of polymerization rate on biological substrates compared to that on water. On water, the lower homologs spread and polymerize rapidly, whereas the higher homologs spread but polymerize slowly. On biological substrates, the lower homologs do not spread or spread slightly and the higher homologs exhibit large spreadabilities and very rapid polymerization rates. Determination of the spreading coefficients for these systems by using the monomers or model compounds confirm the observed spreadabilities. It is proposed that the increased rate of polymerization of the higher homologs on biological substrates may be due to increased catalyst concentrations on these surfaces or to the solubilization of the higher homologs at the interface, making the catalyst sites more available to the monomer. The suggestion is made that if the liquid monomers spread and orient on the substrate and subsequently polymerize, the polymers will maintain the orientation. If such is the case, a technique is available for preparing stereospecific vinyl polymers which may have different spatial configurations depending on the polarity of the liquid substrate upon which they have been allowed to spread and polymerize.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1966.070101101
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  • 20
    Electronic Resource
    Electronic Resource
    Structural characterization of vulcanizates. Part VIII. The N-cyclohexylbenzothiazole-2-sulfenamide-accelerated sulfur vulcanization of natural rubber at 140-180°C. and of synthetic cis-1,4-polyisoprene at 140°C (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 2271-2283 
    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: Vulcanization of natural rubber at 140°C. with a CBS-accelerated sulfur system of conventional type gives rise to a structurally complex network in which the number of sulfur atoms combined per chemical crosslink present increases from 12 to 21 with increasing reaction time. The complexity of the network increases with increasing temperature of vulcanization. Crosslinking of a purified synthetic cis-1,4-polyisoprene proceeds more slowly and yields a slightly more complex network. Despite this overall similarity the natural rubber vulcanizates exhibit considerably higher tensile strengths.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070111114
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