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  • 1
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: To test the molecular parameters concerning gas sorption in polymers, the concentration of CO2, N2O, CO, N2, CH4 and the noble gases Ne, He in glassy poly(butylene terephthalate) films (PBTP) has been studied gravimetrically with a recording microbalance at 25°C. The sorption isotherms exhibit downward curvature to the pressure axis. As neither solubility nor adsorption can explain the experimental results, analysis was carried out based on the dual-sorption model: gas dissolution and microvoid filling are considered as independent sorption mechanisms. The parameters of the dual-sorption model for the mentioned penetrants are determined. The results indicate that for parameter correlation the Lennard-Jones potential parameters give a rough idea, but size exclusion of gases in small diameter microvoids is proposed and special chemical interactions must be considered.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 7-11 
    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 sorption of CO2 and the noble gases Ne and Ar in semicrystalline glassy poly(butylene terephthalate) (PBTP) films was measured by the gravimetric method with a recording microbalance at 298 K. The sorption of CO2 was found to be significantly higher than that of Ne and Ar. This is attributed to a specific interaction between CO2 and PBTP. The sorption isotherm for CO2 was analyzed by the dual-mode sorption model, while the sorption behaviors for Ne and Ar did not follow this model. Their sorption isotherms can be described by the sorption model developed here for the noble gases in PBTP. A critical adsorption pressure p* that is dependent mainly on the relative size of the frozen microvoids and the noble gas atoms is defined in this model. The Langmuir adsorption for describing the sorption in this gas/polymer system in addition to Henry's solubility happens just above this p*, whereas only Henry's solubility takes place below p*. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 13-20 
    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: Sorption measurements of CO2, Ne, and Ar in poly(butylene terephthalate) (PBTP) films were studied by the gravimetric method with a recording microbalance at 298 K in the pressure range of 1-22 bar. The semicrystalline samples were annealed and oriented at 373 K. The sorption isotherms for CO2 in PBTP films in the glassy state can be well described by the dual-sorption theory. The nonlinear sorption behavior of Ne and Ar can be satisfactorily analyzed using the sorption model developed for noble gases in PBTP. For the undrawn annealed films, it has been found that the increment of crystallinity leads to the reduction of the equilibrium gas concentration. For the oriented films, the gas concentration rises with increasing draw ratio. It appears that the sorption behavior for all tested gases in the oriented PBTP films does not depend on the changes of crystallinity and crystalline morphology under extension. The difference of the critical pressure p* indicates the change in the size of the frozen microvoids existing in the noncrystalline phase, which was altered by annealing and drawing. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 128-134 
    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 method of normalization is used to develop the J-R curve fracture toughness characterization for polymeric materials. This method can develop J-R curves directly from load vs. displacement records without a need for an on-line crack monitoring system. It was used previously to develop J-R curves for metallic materials and is applied here for the first time to polymer materials. Single edge notched bend specimens of rubber toughened nylon 6/6 and rubber toughened amorphous nylon are used in this study. The J-R curves from the method of normalization are compared with the results obtained from the multiple specimen method of ASTM Standard E813. The results show that the method of normalization gives reasonable J-R curves; both methods show agreement over the early J-R curve region. In addition the JIc values are determined for each method and compared. Based on this work it is suggested that the method of normalization could be used as a general test method to develop J-R curves for polymeric materials.
    Additional Material: 10 Ill.
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  • 5
    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: Interactions between anions on one polymer chain with cations on another can lead to compatibilization of otherwise incompatible materials. Thus, if 5 mol% of ∼SO3H groups are attached to polystyrene, and 5 mol% of vinyl pyridine is copolymerized with ethyl acrylate, proton transfer occurs upon mixing, and the pairwise attractive interactions between the resultant ions compatibilize the blend. The same has been observed for the styrene-vinyl pyridine and sulfonated polyisoprene polymer pair. Dynamic mechanical and optical properties are used as a measure of compatibilization.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 304-309 
    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 thermomechanical behavior of poly(bisphenol A carbonate) (PC) undergoing cold-drawing (necking) over a large range of temperature and strain rate has been studied. The cold-drawing of PC has been described from a material particle perspective in terms of true stress and strain relationships. The isothermal draw stress is shown to be a material parameter, and the true stress-strain behavior of necked material above the true drawing stress follows conventional treatment by rubber elasticity. Cold-drawing is described as a double glass transition: first, a transition from an isotropic glass to an isotropic rubber at the yield point, then, on unloading after stretching of a rubbery mesophase, a transition from an oriented rubber to an oriented glass.
    Additional Material: 12 Ill.
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  • 7
    ISSN: 0887-6266
    Keywords: in situ composite ; colloidal approach ; masterbatch ; kaolin ; nylon blends ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel in situ composite comprised of kaolin clay fillers and polyamide 6 (Nylon-6) was synthesized via a colloidal approach by suspending kaolin particles in aqueous caprolactam and then polymerizing the caprolactam under elevated temperature and pressure. This in situ polymerization technique enables the deposition of nylon molecules directly onto the filler surface. It offers a much larger contact surface area for the nylon molecules to interact with the filler particles and enhances filler/matrix interaction through polymer miscibility. The kaolin particles were shown to be uniformly dispersed in Nylon-6 matrix without appreciable agglomeration. In the highly clay-loaded composites such as the 50/50 kaolin/Nylon-6 in situ composite, the deposited nylon molecules probably form a coated layer on the filler particles. This kind of nylon coated fillers may be applied as a reinforcing entity to commercial Nylon-6 or -;66 by improving particle dispersion and melt processability. The 50/50 kaolin/Nylon-6 in situ composites have been used as a masterbatch for blending with commercial Nylon-6 and Nylon-66 to take advantage of their good properties and to reduce cost. Rheology and mechanical properties of the masterbatch/nylon composites have been investigated in comparison with those of the conventional melt-mixed composites. The improvement of rheological and mechanical properties of the in situ composites has been discussed in relation to the composite structure. © 1996 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1761-1768 
    ISSN: 0887-6266
    Keywords: Filled composite ; colloidal polymerization ; kaolin ; Nylon-6 ; in-situ composite ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A mineral-filled in situ composite was prepared by a colloidal approach by first suspending kaolin filler particles in aqueous caprolactam, and then polymerizing caprolactam in situ at high pressure and temperature. The purpose of this colloidal in situ polymerization is to improve particle dispersion and to enhance interaction of the filler to the polymer matrix. X-ray diffraction studies of the in situ kaolin/Nylon-6 composites revealed that the x-ray peak corresponding to the α-crystal form of Nylon-6 diminished with increasing kaolin loading, while the γ-crystal structure became more pronounced. The degree of crystallinity of Nylon-6 remained fairly unchanged with the kaolin loading level in the in situ composites. Calorimetric and dynamic mechanical studies exhibited that the glass transition temperature of the resulting composite increased significantly with increase in kaolin concentration, suggesting strong filler-matrix interaction at the kaolin/Nylon-6 interface. Scanning electron microscopic (SEM) results showed uniform filler dispersion in the in situ composites relative to the conventional melt-mixed composites. Modulus and tensile strength of these in situ composites were found to be distinctively higher than that of the conventional melt-mixed kaolin/Nylon-6 composites. However, as typical for composite materials, drawability and fracture toughness decreased with increasing kaolin loading. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1047-1051 
    ISSN: 0887-6266
    Keywords: polyethylene ; rapid fracture ; slow fracture ; blends ; model copolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resistance to slow crack growth (SCG) was measured in binary blends of high density polyethylene (HDPE) and 5-10% concentrations of model ethylene-butene random copolymers by measuring the time to failure (tf) under a constant stress intensity. An increase of tf with the addition of the copolymer if the copolymer could crystallize and the increase was greater the higher branch density. The copolymer with 117 branches/1000C could not crystallize and therefore its blend had a tf that was less than that of the HDPE. The fracture energies of the blends as determined by their resistance to SCG were compared with the energy by rapid fracture, Jc, as previously measured by Rhee and Crist. It is concluded that SCG is more sensitive to variations in the microstructure than is rapid fracture and that the differences in SCG behavior can be qualitatively explained in terms of the differences in microstructure of the blends. ©1995 John Wiley & Sons, Inc.
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