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  • Articles  (1,331)
  • Chemistry  (1,331)
  • 1985-1989  (1,331)
  • 1987  (1,331)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (1,331)
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  • Articles  (1,331)
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  • 1985-1989  (1,331)
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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1021-1034 
    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: Equations are derived that relate the orientation of “pseudo-affine” reoriented structural units after a biaxial deformation to the degrees and the directions of the effective drawings. The connection between these drawing parameters and those externally applied is analyzed in detail. It is shown how a comparison of these two sets of drawing parameters allows conclusions regarding the distribution throughout the material of the stresses that cause the deformation, the inhomogeneity of the deformation, and the role of non-orienting flow during deformation. In particular, the orientation of biaxially drawn poly(ethylene terephthalate) films is investigated, and it is shown what general information can be obtained on the deformation behavior of this material on the basis of these considerations.
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1059-1068 
    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: Scale-up from small laboratory size extruders to large production size extruders is a procedure of great practical importance. Many scale-up rules and theories have been proposed in the past, however it is not always clear how the different scale-up methods will affect extruder performance. A basic analysis of scale-up in plasticating single screw extruders is developed from which the effect of a certain scale-up strategy on extrusion performance can be evaluated in terms of solids conveying, melting, melt conveying, mixing, residence time, heat transfer, power consumption, and specific energy consumption. Various existing scale-up theories are evaluated and compared using the basic analysis. A number of existing scale-up theories have some significant drawbacks, in particular with non-constant specific energy consumption and imbalance between melting rate and pumping rate. Conditions that are desirable to achieve in scale-up are enumerated and ranked in terms of importance. This leads to two new scale-up methods that result in constant mechanical specific energy consumption and high throughput rates. The first scale-up method keeps the specific surface area constant. This scale-up should work well for high values of the Brinkman number. However, at low values of the Brinkman number, the melting rate may be insufficient. The second scale-up method keeps the melting rate at low Brinkman number equal to the pumping rate and, thus, should be useful in cases where the first scale-up method cannot be used.
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987) 
    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
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1128-1136 
    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 plane strain fracture toughness and fracture mechanisms of several tough engineering plastics have been studied and compared with poly(methyl methacrylate) (PMMA), a relatively brittle polymer. The tough polymers all are observed to form a multiple craze zone at the crack tip, which is shown to be the primary source of plane strain fracture toughness in these materials. The multiple craze zone is retained during slow crack growth but is metastable, and at a critical stress intensity and associated crack velocity, the system passes through a transition to a greatly accelerated single craze mode of unstable propagation.
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  • 5
    Electronic Resource
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1148-1155 
    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 optical properties of bisphenol-A polycarbonate resin as described by the complex index of refraction, N = n - ik, are derived by Kramers-Kronig analysis of experimental absorption and reflectance data obtained in the range 40μm ≥ λ ≥ 105 nm. Electronic absorption processes in polycarbonate are characterized by two broad absorption peaks centered at ∼200 and ∼100 nm.
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  • 6
    Electronic Resource
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1182-1186 
    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: Three-layer coextruded blown (either blend or composite) films, made of low-density polyethylene and linear lowdensity polyethylene (1:1 ratio) of identical density, were compared. The tensile properties of both systems are nearly as high as those of the linear polyethylene while high strain rate properties including impact strength and tear resistance of the composite film are superior. Some structural insight was obtained by thermal analysis and thermoelastic measurements. Structure property relationships are discussed in light of the unique behavior, structure, and morphology of linear low-density polyethylene. The two polyethylenes are only compatible to a rather limited extent mainly affecting their blend behavior. However, a strong mutual reinforcement effect was observed.
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  • 7
    Electronic Resource
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1203-1208 
    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: A Viton copolymer containing vinylidene fluoride (VF2) and hexafluoropropylene (HFP), and a terpolymer containing VF2, HFP, and tetrafluoroethylene (TFE) were cross linked using varying amounts of Bisphenol AF to yield two series of fluoroelastomer networks, Stress-strain isotherms in elongation were determined for these samples at several temperatures and at two degrees of swelling with phenyl acetate. Strain-induced crystallization was observed, as evidenced by upturns in the isotherms at high elongations. It appears to be more pronounced in the terpolymer samples, presumably because the TFE units not only can crystallize themselves, but can co-crystallize with the VF2 units. The crystallization was found to persist upon moderate increase in temperature, but was suppressed when the networks were swollen, Thermoelastic (force-temperature) measurements were used to obtain values of the fraction fe/f of the elastic force that is due to energetic effects. Negative values were obtained for both types of samples and, in the case of two samples studied in detail, their magnitudes increased with increase in elongation. The magnitudes were larger and the increases more pronounced in the case of the terpolymer networks, as would be expected from a greater tendency for straininduced crystallization.
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  • 8
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1221-1228 
    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 transesterification reaction of molten ethylene and vinyl alcohol copolymers (EVA), in presence of paraffinic alcohols and basic catalysts, leads to high conversion of the ester groups to secondary alcohol in both discontinuous and continuous processing equipment. Various kinds of alcohols and two different catalysts were used. Sodium methoxide is a powerful catalyst for the equilibrated transesterification reaction, but we also observed side reactions, such as cross-linking with low-molecular-weight alcohols and hydrolysis of the catalyst followed by partial saponification of the EVA. Kinetic studies were performed in the presence of dibutyltin dilaurate, an efficient catalyst without any side reactions. The solubility of the main alcohol reagents was verified by diffusion measurements. The general reaction scheme and the related kinetics, corresponding to a homogeneous system, lead to a fair evaluation of the rate constants.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1252-1257 
    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 mechanical properties of polyurethane-unsaturated polyester interpenetrating polymer networks (IPNs) that were prepared by reaction injection molding (RIM) process were measured with variations In composition, cross-link density, and relative reaction rate. From dynamic mechanical analysis (DMA), it was found that the two component polymers had a good compatibility over the whole composition range. The tensile strengths of the blends were greater than those of the pure components and had a maximum value at 50/50 composition. The modulus of elasticity and surface hardness decreased and the impact strength increased as the polyurethane content was increased, but the changes were not high at low polyurethane content, below 50%. For higher cross-link density, the compatibility was enhanced and the mechanical properties were improved. When the reaction rates of the components were different, some extent of phase separation was found in DMA and the properties were affected adversely.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 487-503 
    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: Tensile properties of polyethertherketone (PEEK) have been studied at 125, 25, and -100°C for thin films prepared with different thermal histories. Initial morphology was controlled by rate of cooling from the melt. Amorphous films resulted from quenching the melt, while semicrystalline films were obtained by cooling the melt at different rates, or by crystallization of the rubbery amorphous state. The films were characterized using density, X-ray scattering, differential scanning calorimetry, and infrared spectroscopy. Scanning electron microscopy was used to examine fracture surfaces. Degree of crystallinity and rate of cooling from the melt affected the tensile properties at all test temperatures. For films with nearly the same degree of crystallinity, those which were more slowly cooled from the melt fractured at the lowest strain. The amorphous films were most tough, drawing to 233% at -100°C and to over 500% at 125°C. Films crystallized from the rubbery amorphous state had stress-strain behavior intermediate between that of the amorphous and melt-crystallized films at all test temperatures. Density measurements on the drawn material indicate that void formation occurs simultaneously with the formation of fibrillar crystals. Necking resulted in density increases for amorphous films, and density decreases for the semicrystalline films.
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  • 11
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 577-606 
    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: Fatigue tests have been conducted on polystyrene bars molded at different pressures and having different post-molding thermal histories. Fatigue crack propagation rates were not sensitive to molding or thermal history but in unnotched bars initiation seemed to happen more quickly in bars aged for long periods at room temperature or annealed at elevated temperature. Fractographic studies showed that initiation occurred at favored sites and that the skin/core morphology affected crack growth. Prolonged storage of polystyrene bars at -85°C promoted significant physical property changes (stiffness and density). These changes appeared to be at least partly reversible with rapid recovery occurring within the first 24 h after restoring to room temperature.
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  • 12
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 641-656 
    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: Chitosan has been prepared from prawn shell and crab shell chitin. The molecular weight of the material derived from prawn shells is higher than that obtained from crab shell. The molecular weight, tensile strength, elongation at the break, and hydrophilic properties of chitosan are extremely dependent on the degree of deacetylation achieved when chitin is hydrolyzed to chitosan. Graft copolymers have been prepared with chitosan and a series of vinyl monomers using both heterogeneous and homogeneous reaction conditions. The hydrophilic properties of chitosan can be modified by blending with poly(vinyl alcohol).
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  • 13
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 693-702 
    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 new technique for quantifying the amount of multimolecular microgel material in water-soluble polymers is described. The enhanced velocity of the large microgels during flow through a 25 μm capillary is the basis for a separation between the microgels and dissolved polymer. With the use of laser-excited fluorescence detection, the arrival of fluorescently-tagged polyacrylamide samples at a downstream location is recorded. The presence of small amounts of microgel has a deleterious effect on the ability to filter polymer solutions. Analysis of samples before and after filtration suggests that a significant amount of microgel material above 8 μm in diameter is present in samples that exhibit poor filterability characteristics. Treatment of a sample with base is found to improve filterability and to decrease the amount of microgel in the sample.
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  • 14
    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: In order to reduce the internal stress in a cured epoxy resin, submicrometer-sized poly(butyl acrylate) (PBA)/poly(methyl methacrylate) (PMMA) core-shell particles having cross-links were dispersed in the resin prior to curing. For the introduction of cross-links, monoethylene glycol dimethacrylate or glycidyl methacrylate monomer was copolymerized. Cross-links in the PBA core reduced the shrinkage of the cured epoxy resin, and cross-links at the PMMA shell produced a strong interaction with the epoxy matrix. The internal stress was reduced effectively by the introduction of cross-links.
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  • 15
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 505-520 
    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 effect of processing conditions on the morphology of polyetheretherketone (PEEK) graphite reinforced composites (APC-2) has been characaterized. Differential scanning calorimetry was utilized to examine the effect of quench rate on recrystallization where a change in mechanism was observed at a rate of 5°C/min. Optical microscopy revealed a decrease in spherulite size and a reduced degree of transcrystallinity at the graphic fiber surface with increasing quench rates. Dynamic mechanical analysis indicated a change in relaxational processes in the Tg region with varying quench rates.
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  • 16
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 533-549 
    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: Penetrant transport through and solute release from continuously swelling polymers is viewed as a process associated with major structural changes in the polymer morphology. Changes in the diffusivities of penetrant and solute reflect a free volume mechanism for transport. The polymer is initially glassy with a uniform dispersion of solute. After the system is placed in contact with a thermodynamically good penetrant, a glassy/rubbery phase transition occurs at a well defined swelling interface. The Fickian equations with concentration-dependent diffusivities and moving boundaries are solved simultaneously in polymer-fixed coordinates. A constitutive relation is used to describe the effect of macromolecular relaxations on the rate of volume expansion as the polymer swells. The penetrant fractional uptake, solute fractional release, sample dimensions, swelling front position, and instantaneous swelling interface number are determined and related to the nature of the swelling process.
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  • 17
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 551-576 
    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: Measurements were made of infinite dilution diffusion coefficients of volatile liquids in amorphous polymers at elevated temperatures, using inverse gas chromatography. The liquids used were benzene, toluene, ethylbenzene, and n-decane. The polymers used were polystyrene and poly(vinyl acetate), and temperatures ranged from 30°C to 120°C above the glass transition temperatures of the polymers. Packed chromatographic columns were used to obtain data of the variation of the plate height with the average gas velocity, which was then used to determine diffusion coefficients with the aid of the van Deemter equation. In the present investigation, we have used different sizes of glass beads (0.3, 0.5, 0.6, and 1.0 mm in diameter), depending on the system temperature and the polymer/solute pair chosen. An attempt was made to correlate on the diffusion coefficient D measured at various temperatures T, using in Dζ as ordinate and 1/[(K22 + T - Tg2)/Tc] (hereafter referred to as the reciprocal of reduced free volume temperature, 1/TRF) as abscissa, in which ζ = M1/2/T1/2cV1/3c, M being the molecular weight, Tc the critical temperature, and Vc the critical volume of the solute, K22 is a free volume parameter of the polymer, and Tg2 is the glass transition temperature of the polymer. It has been found that such plots give rise to two linear regions having different slopes, separated by a critical value of 1/TRF. The critical value of 1/TRF is found to be insensitive to the type of solute and the type of polymer used. We have concluded that the infinite dilution diffusion coefficient of volatile liquids in amorphous polymers is controlled predominatly by the free volume of polymer above a critical value of 1/TRF, but energy effects are significant below the critical value of this parameter. In order to apply the generalized relationships in conjunction with gas chromatographic measurements, the results of this study indicate that, for values of 1/TRF larger than a critical value, which is approximately 4.8, the following expression, In Dζ = α + b/TRF, may be used to predict infinite dilution diffusion coefficients of volatile liquids in amorpous polymers at elevated temperatures, in which α is a constant, independent of the type of solute, and b is approximately a constant for a given polymer in the free volume region, independent of the type of solute. More experimental studies are needed, particularly for temperatures higher than those reported in this study, to corroborate and/or extend the correlations presented here.
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  • 18
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 241-241 
    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
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  • 19
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 289-303 
    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: Dynamic shear experiments in the linear range of deformation and extensional tests at constant strain rate have been carried out on a linear low-density polyethylene (LLDPE) melt and on two branched low-density polyethylene (LDPE) melts with different amounts of long-chain branching. Both the dynamic shear moduli and the tensile stress obey the time-temperature superposition principle. A simple model based on a nonaffine generalized Maxwell model with two relaxation times is proposed to describe the rheological behavior in elongation of these melts. Close agreement between the model and the experimental data can be obtained by adjusting the two relaxation times and the “slip parameter” of entanglements. The variations of these parameters with strain rate and their relationship with molecular structure are discussed.
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  • 20
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 329-351 
    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 kinetics of tetrabutyl titanate catalyzed transesterification of dimethyl terephthalate with poly(tetramethylene ether) glycol of various molecular weight has been studied in the presence and absence of 1,4-butanediol. Detailed analysis of experimental data with a proposed kinetic model indicates that the equal reactivity hypothesis for functional groups is valid within a wide range of experimental conditions studied. It is also found that the reactivity of hydroxyl groups of macrodiols such as poly(tetramethylene ether) glycol is independent of the chain length of the polymer. Effect of various reaction parameters on the transesterification rate and the resulting product composition is also discussed.
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  • 21
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    Journal of Applied Polymer Science 33 (1987), S. 1427-1444 
    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: Filaments of poly(butylene terephthalate) were prepared by melt spinning with take-up velocities in the range 1000-5600 m/min. Two polymers with different molecular weights were used (intrinsic viscosities of 0.75 and 1.0 dL/g). The filaments were characterized using measurements of density, birefringence, shrinkage, thermal properties (differential scanning calorimetry), crystal size, crystalline orientation and phases present (wide angle X-ray diffraction), and tensile mechanical properties. Filaments spun from the 0.75 IV polymer with a mass throughput of 6 g/min at 1000 m/min have essentially amorphous structures, while higher take-up velocities result in α-form crystals or, at the highest take-up velocity, a mixture of α-form and β-form crystals. Only α-form crystals were detected in the higher IV polymer. Crystal size varied with crystallographic direction but generally increased as take-up velocity increased. At the lowest take-up velocities the filaments increased in length during thermal shrinkage measurements. With increasing take-up velocity the shrinkage became positive and continued to increase until reaching a maximum in the range of the highest sprinning speeds. This behavior correlates with the variation of the orientation factors of the amorphous phase. A plateau was observed in stress versus strain curves corresponding to strain-induced transformation from α-form to β-form crystals. The length of this plateau increased with increase of take-up velocity and the α-form crystal content in the sample. Both morphology and physical properties varied with polymer molecular weight and melt spinning conditions.
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  • 22
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    Journal of Applied Polymer Science 33 (1987), S. 1479-1485 
    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 graphic multiple peak resolution method by wide angle X-ray scattering (WAXS) pattern was described and used to estimate the interplanar spacings, crystallinities, and crystalline sizes of eight poly(ethylene terephthalate) (PET) fibers. The values for interplanar spacings of Dacron 54 suggested that the unit cell model by Daubeny et al. was appropriate for Dacron fibers. In general, crystallinities of the eight PET fibers ranged from 44.7% for Dacron 54 to 62% for Dacron 56 with the copolymers in between. Crystallinity by density measurements was determined and compared to that by WAXS in both fabric and ground fiber forms. Crystallinity values for each fiber derived by these three methods were different. For each fiber, crystallinity was lowest by WAXS in the ground fiber form, followed by the density measurement and WAXS in the fabric form.
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  • 23
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    Journal of Applied Polymer Science 33 (1987), S. 1487-1493 
    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: Poly(butadiene-maleic anhydride) was aminated with methoxypropylamine. Although this reaction product (APBM) was easily soluble in water, when APBM was supported on activated alumina, APBM/alumina hybrid materials (HM) removed dodecylbenzenesulfonate (DBS) solutes in water. The effects of the supported amounts and of the initial concentrations of DBS on the removed amounts were studied.
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  • 24
    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: It was studied how to localize carboxyl groups at the particle surface in a preparation of styrene (S)/butyl acrylate (BA)/methacrylic acid (MAA) polymer emulsion. The relative distribution of carboxyl groups in the emulsion was determined by conductometric titration method: in serum, at surface, and inside particle. By seeded (two-stage) emulsion polymerization that S-BA-MAA terpolymer emulsion was first prepared at low pH and then second stage polymerization of S-BA was continued at high pH, S/BA/MAA polymer emulsion particles in which carboxyl groups are localized predominantly at the surface could be prepared.
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  • 25
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    Journal of Applied Polymer Science 33 (1987), S. 1601-1607 
    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: An aromatic polyamide-imide (PAI) film was reinforced with a plain cloth of aromatic polyamide fiber (Du Pont, Kevlar 49). The mechanical properties of the composite film were investigated by examination of the temperature dependencies of tensile dynamic mechanical properties, stress relaxation, and tensile stress-strain behaviors. The softening temperature of the composite film was lower than that of a homogeneous PAI film. At a high temperature, Kevlar fibers may act as a thermal conductor and lower the softening point of the PAI composite. The mechanical properties of the composite film at a high temperature are mostly controlled by the PAI matrix.
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    Journal of Applied Polymer Science 33 (1987), S. 1623-1639 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Stress relaxation measurements in tension have been made on nitrile rubber vulcanizates containing short jute fibers. The effects of strain level, bonding system (silica-resorcinol-hexa), fiber orientation, fiber content, temperature, and prestraining on the rate of stress relaxation have been investigated. Existence of a relaxation mechanism within the first 200 s is reported.
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  • 27
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    Journal of Applied Polymer Science 33 (1987), S. 1649-1661 
    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: In poly(p-phenylene terephthalamide-co-ethylene terephthalate) the rigid segments of p-phenylene terephthalamide are aggregated as crystalline domains above the weight fraction of the rigid segments, 6 wt%. The rigid segments disturb the crystallization of the flexible segments of poly(ethylene terephthalate) (PET) and are preferentially contained in the amorphous phase of the PET segments. The crystallinity of the PET segments decreased with increasing the content of the rigid segments in the copolymers and the glass transition temperature is decreased by the decrease of the crystallinity below the weight fraction of the rigid segments, 6 wt%, in spite of the depression of micro-Brownian motion of the PET segments due to the rigid segments. The values of Young's modulus E, yield stress σy and breaking stress σb for the zone-drawn copolymer were conspicuously increased by the rigid segments contained in it, in comparison with those of the zone-drawn PET homopolymer. Such higher values of E, σy, and σb of the copolymer are originated by greater increases in the orientation of amorphous chains in the copolymer. The rigid segments in the amorphous phase effectively depressed the thermal shrinkage of the zone-drawn and the zone-annealed copolymers.
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  • 28
    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 new, simplified technique for obtaining the kinetic parameters of an autocatalyzed cure reaction from isothermal DSC measurements is presented. The method is appropriate to reactions that have a zero initial rate and relies solely upon characteristics of the exotherm peak with no assumptions being made about the overall reaction order. This technique is illustrated by obtaining the phenomenological cure kinetics of a commercial epoxy film adhesive. The derived kinetic model reproduces the measured isotherms in their entirety. In addition, the predictive capability of the model is demonstrated by comparison with an independent measurement of the adhesive's low temperature curing behavior. Glass transition temperature measurements are also made on partially cured samples and a good correlation with the degree of cure is found.
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    Journal of Applied Polymer Science 33 (1987), S. 1735-1743 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Copolymerization reactions of di-(tri-n-butyltin) itaconate with styrene and methyl methacrylate were carried out in solution at 70°C using 1 mol% azobisisobutyronitrile as a free radical initiator. The copolymer compositions were determined by chemical analysis as well as from 1H-NMR data. The monomer reactivity ratios for copolymerizations of di-(tri-n-butyltin) itaconate with styrene and methyl methacrylate have been found to be r1 = 0.228, r2 = 0.677, and r1 = 0.220, r2 = 1.635, respectively. The sequence distribution of the triad fractions were calculated from reactivity ratios and compared with those obtained from 1H-NMR data.
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    Journal of Applied Polymer Science 33 (1987), S. 1777-1784 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A simple interferometric technique is described for monitoring thickness changes in solution-cast polymer films as they are dried and cured. This paper follows a freshly spun solution of polyamic acid in NMP as it is converted into a cured polyimide film of 6 μm in thickness. The technique is shown to be nearly quantitative despite the effects of thermal expansion and cure-related refractive index changes.
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    Journal of Applied Polymer Science 33 (1987), S. 1829-1834 
    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
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  • 32
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    Journal of Applied Polymer Science 33 (1987), S. 1835-1842 
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    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
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  • 33
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    Journal of Applied Polymer Science 33 (1987), S. 1859-1871 
    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: Poly(starch-g-(1-amidoethylene)) can be formed by aqueous, free radical polymerization of 2-propenamide on lintnerized, potato starch. Initiation is by attack of cerium ions (+IV) on the D-glucopyranosyl units of starch. The reaction produces a water-soluble thickener with molecular properties of the product controlled, in part, by the gel effect induced in virtually all syntheses. Yield of product varies from 38 to 100% with yields of 90-100% being common. Products containing less than 50 wt % sidechain were found to be difficult to dissolve once they were recovered from the synthesis mixture. A sample with a design molecular weight of 0.8 × 106 and 4 grafts per backbone formed 3.9 wt % of a water-insoluble solid in the reaction mixture. The solid, which had a composition similar to that of the reaction mixture, may be the result of selective reaction within the distribution of backbone molecules.
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  • 34
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    Journal of Applied Polymer Science 33 (1987), S. 1933-1941 
    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 variety of crosslinked phenol-, or derivatized phenol-formaldehyde polymers have been synthesized. The phenol derivatives included o- and p-cresol, p-nonylphenol, m-pentadecylphenol, and raw and distilled cashew nutshell liquid. The derivatives were copolymerized with phenol and formaldehyde using sulfuric acid as catalyst to yield novolak-type prepolymers, which were then cured with hexamethylenetetramine. Thermogravimetric analysis was used to evaluate the thermal stability of the cured resins. It was found that the thermal stability of the resins decreased with increasing amounts of cashew nutshell liquid, with distilled cashew resins being slightly more thermally stable than raw cashew resins. The thermal stability of resins containing substituted phenols with alkyl chains was observed to increase from n-pentadecylphenol to cresol to phenol. The trend in thermal stability of the resins may be explained on the basis of alkyl groups being less thermally stable than aromatic rings. The amount of hexamethylenetetramine used to cure the prepolymers also influences the thermal stability of the resins. It appears that a level of 10 to 15% hexamethylenetetramine maximizes the thermal stability of the resin.
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    Journal of Applied Polymer Science 33 (1987), S. 971-983 
    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 synthesis, properties, and polymerization of an acetylene terminated monomer are described. The monomer melts and is thermally polymerized at 150°C and then at 300°C in an air environment. From the liquid stage, the monomer can be fabricated into moldings, castings, and prepregs. As initially cured, the polymer is an insulator. By further thermal processing at elevated temperatures in an inert atmosphere, conductivity can be controllably introduced into the polymer; for example, at 600°C a conductivity of 3.3 (Ω-cm)-1 is obtained. Exposure of these conductive polymers to either boiling water for 1000 h or temperatures 100°C below their maximum process temperature (400-500°C) for 500-800 h did not produce any significant change in conductivity.
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    Journal of Applied Polymer Science 33 (1987), S. 997-998 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Applied Polymer Science 33 (1987), S. 1089-1102 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: In this investigation, experimentally measured radial birefringence profiles are compared to internal stress distributions as predicted by a mathematical model. A direct indicator of the degree of molecular orientation, fiber birefringence, is found to correlate well with the stress distributions as calculated from radial temperature variations. In an initial study of glass fibers, no radial birefringence profiles are found, indicating that any residual stresses present are small. In polystyrene fibers, however, large radial variations in birefringence are observed and are shown to be directly related to the calculated internal stresses.
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    Journal of Applied Polymer Science 33 (1987), S. 1157-1171 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Improved synthesis of polydiallylamine provides ready access to an entire family of amide-functionalized polymers. Complete conversion to the acetamide derivative was attained under mild conditions. Formation of the formamide polymer required harsher conditions and did not give complete functionalization. The formamide polymer displayed typical polyelectrolyte behavior caused by residual amine units. Complexation with iodine and transition metal cations was strong as shown by UV, IR, and 13C-NMR evidence indicating potential of these polymers for trace metal recovery, waste water treatment, and antiseptic formulations.
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  • 39
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    Journal of Applied Polymer Science 33 (1987), S. 1455-1471 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The behaviors of iron, nickel, and zinc dialkyl dithiocarbamates were compared with the corresponding thiuram disulphide in their reaction with cumene hydroperoxide (CHP) at 110°C. The metal complexes exhibit both homolytic and heterolytic processes and transformation products formed during the above reactions and not the initial metal complexes were found to be responsible for the heterolytic decomposition process. However, the nature of the initial transformation products in the case of the iron and nickel complexes differed from those of the corresponding zinc complex. In the former case the corresponding disulfide was shown to be the initial transformation product while there was no evidence for the formation of disulfide in the case of the zinc complex. This difference appears to be responsible for the observed different kinetic behavior of CHP decomposition in the presence of the nickel and iron complexes from that in the presence of zinc. This thiuram disulfide behaves quite differently from the metal complexes in that heterolytic decomposition of hydroperoxide predominates at all molar ratios of the disulphide to the CHP. The hydroperoxide decomposition curves in this case show only one step in contrast to the metal complexes which show a multistep behavior, and this was shown to correspond to the third catalytic stage in the reaction of the metal complexes. Comparison of the rate constant of this step with that of the final step of the metal complexes shows a close resemblance to the case of the iron and nickel and is quite different from that of the zinc complex, confirming the intermediacy of the disulfide in the former cases but not in the latter.
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    Journal of Applied Polymer Science 33 (1987), S. 1517-1523 
    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: Understanding the deformation behavior of an amorphous thermoplastic, e.g., poly(ethylene terephthalate) (a-PET) and one of semicrystallinity, viz., i-PP, can be is of both fundamental and practical importance. Much has been done to study the influence of temperature and strain, but not the influence of deformation conditions on the three-dimensional orientation of many thermoplastic. In this study we consider the incremental effect of hydrostatic pressure and process geometry on strain-induced deformation. a-PET has been free drawn (i.e., no hydrostatic pressure) isothermally on a tenter frame device. The hydrostatic, equibiaxial deformation was achieved by a forging process involving squeezing between two circular plates. These two processes have been carried out at a series of deformation rates, with the three-dimensional refractive index measurements having been made on the PET and i-PP films using a modified Abbe refractometer, as per Samuels. The reported trirefringence measurement provides a sensitive scale for the planar deformation.
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    Journal of Applied Polymer Science 33 (1987), S. 1567-1577 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: An analysis is given of the critical internal pressure P at which a circular debond (“blister”) will grow in size, in terms of the tensile modulus E and thickness t of an adhering layer, and the strength Ga of its adhesion to a rigid substrate. Measurements of blow-off pressure are reported for adhering layers of pressure-sensitive tapes having widely different effective modulus and thickness, and with blisters having a range of diameters. Satisfactory agreement is obtained with the theoretical predictions, suggesting that the theory is basically correct in assuming that relatively thin layers behave like elastic membranes. Attention is drawn to the unusual form of the dependence of the debonding pressure P upon the resistance Et of the layer to stretching and upon the detachment energy Ga: P4 ∝ EtGa3. Even though the adhering layer is assumed to be linearly elastic, the markedly nonlinear (cubic) relation between pressure P and volume V of the blister, or maximum height y, leads to this unusual result. The detachment energy is given by a particularly simple function of the pressure P and maximum deflection y of the blister: Ga = 0.65Py, independent of the stiffness of the adhering layer and diameter of the blister.
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    Journal of Applied Polymer Science 33 (1987), S. 1585-1600 
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    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: Linear viscoelastic properties are found to be a sensitive measure of flow-induced structural changes in a block copolymer. Styrene-butadiene-styrene block copolymer (SBS) with 26% polystyrene (PS) forms a macrostructure in the quiescent state with grains of the order of 1-10 μm. Within each grain, phase separation gives rise to a regular two-phase microstructure with cylindrical PS domains with radius of the order of 200 Å. Large-amplitude oscillatory shear (γ = 4.5) at temperatures between 139 and 181°C was applied to after the grain structure with the objectives of removing the discontinuities at the grain boundaries and of aligning the domains into a continuous ultrastructure. The SBS behaved like a solid (tan δ 〈 1 at low ω) before and like a liquid (tan δ 〉 1) after shear modification. This change expressed itself in the removal of the long relaxation times from the linear viscoelastic spectrum; the intermediate and low relaxation times were not affected by the shear modification. The viscoelastic spectrum slowly recovered during annealing with recovery times of the order of the longest relaxation time of the quiescent structure. Birefringence studies showed that the SBS did not recover into its original grain structure but into a highly oriented domain structure. The discontinuities at the grain boundaries could not be removed completely.
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    Journal of Applied Polymer Science 33 (1987), S. 1675-1682 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: PAN shows two glass transition temperatures. Study of dynamic mechanical properties, especially loss tangent, as a function of temperature enables one to study changes in these temperatures after treatment with a few selected solvents, both for the control as well as thermally treated PAN. Results show that two temperatures behave differently for treatments with different solvents. Aromatic solvents affect lower Tg whereas nonaromatic solvents increase the upper Tg preferentially. Thermomechanical analysis confirms the above results. Such behavior is explained on the basis of interaction of the solvent with two characteristic types of binding types in PAN responsible for two transition temperatures.
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    Journal of Applied Polymer Science 33 (1987), S. 1699-1714 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Mark Houwink coefficients and molecular size parameters are presented for 31 unfractionated samples of polyacrylamide and hydrolyzed polyacrylamide in 0.5M and 1M aqueous NaCl. Polymers investigated include polyacrylamide, plus 10, 20, 50, 70, and 100 mol % poly(sodium acrylate). Their solution characteristics were studied by gel permeation chromatography, intrinsic viscosity, and light scattering techniques. A density function and heterodispersity index was assigned to each polymer sample due to the polydispersity of the molecular weight distributions. This technique improves the intrinsic viscosity-molecular weight correlation for heterodisperse commercially synthesized polymer systems. The intrinsic viscosity of these commercial compounds will yield useful estimates of their molecular weight, in spite of their obvious heterogeneity.
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    Journal of Applied Polymer Science 33 (1987), S. 1745-1761 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Wear behavior correlations with morphology and orientation directions have been established from commercially produced nylon 6 with different draw ratios between 1 and 7 approximately. The wear rate is least in a direction perpendicular to the draw direction for highly drawn samples. It correlates with surface microstructure and the inherent molecular characteristics induced by sample preparation. Well-characterized polymer specimens were used in this investigation.
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    Journal of Applied Polymer Science 33 (1987), S. 1823-1828 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Applied Polymer Science 33 (1987), S. 1843-1848 
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    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
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    Journal of Applied Polymer Science 33 (1987), S. 1849-1852 
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    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
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  • 49
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    Notes: Graft terpolymers of starch, 2-propenamide, and sodium 2-methyl-3-imino-4-oxohex-5-ene-1-sulfonate can be made by cerium-IV-initiated, free-radical polymerization of an aqueous monomer mixture on starch. Synthesis is conducted on aqueous, gelled, lintnerized potato starch at 30°C under a nitrogen atmosphere. Yields range from 50 to 100 wt % and products contain 9-52 wt % starch, 1-51 wt % 1-acidoethylene, and 18-65 wt % sodium 1-(2-methylprop-2N-yl-1-sulfonate)amidoethylene. Repeat unit ratios in the reaction product approximate monomer ratios in the reaction mixture. Fraction of starch grafted in a reaction decreases as the mole fraction of sulfonated monomer in the reaction mixture increases. No proof has been found for grafting of synthetic side chains to starch in monomer mixtures containing only sulfonated monomer. Starch graft copolymers with side chains composed of 1-amidoethylene units and a sulfonated 1-amidoethylene unit derivative, 1-(sodium[2-methylprop-2N-yl-1-sulfonate])amidoethylene, are water-soluble, thickening agents. The rheology of solutions of these copolymers is a function of the ratio of nonsulfonated to sulfonated repeat units in the synthetic chains of the molecule. Aqueous solutions of these products are shear thinning and have power law exponents which decrease 1) with increasing product concentration or 2) as the nonsulfonated to sulfonated repeat unit ratio moves toward 3/1. Limiting viscosity number of product in water decreases with increasing shear rate of measurement or with increasing salt concentration of the solvent. Formulas are derived from the theories of Kirkwood and Flory which show that for copolymers with constant molecular weight, expansion coefficient, and limiting viscosity number increase as the fraction of sulfonate-containing repeat units in the chain increase. This theoretical requirement and the limiting viscosity data for groups of samples prepared under identical synthesis conditions are used to show that molecular weight of the graft copolymer decreases as the fraction of sulfonated repeat units in the copolymer increases. Screen factor measurements show product solutions to be viscoelastic.
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    Journal of Applied Polymer Science 33 (1987), S. 2623-2635 
    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: Geometric requirements, avoidance of boundary conditions, and focus on configurational properties have suggested mean field formulation of the many chain problem using discrete single chain Gaussian partition functions. Mean field account of energetic, combinatorial, and configurational contributions to the free energy provides correct reduction in the limit of remote confinement and avoidance of double counting of interactions. Strong influence of surface adsorption on configurational and global properties of spatial distribution is predicted to occur at lower concentrations. The interplate surface tension has been calculated in decoupled conditions (large separation distances between plates). Numerical results predict an approximate power law dependence of the surface tension on the concentration with exponent ∼ 1.3. Perfectly repulsive boundaries and athermal solvent conditions have been assumed for this calculation.
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    Journal of Applied Polymer Science 33 (1987), S. 2651-2656 
    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: Trimethylammonium-2-hydroxypropyl (TMAHP) derivatives of spruce wood meal (SWM) and holocellulose of this specia were prepared by the reaction of wood meal with 3-chlor-2-hydroxy-propyltrimethylammoniumchloride (CHMAC) in alkaline medium. The TMAHP samples were fractionated and yields and exchange capacity (Q) of individual fractions were compared with beech and aspen fractions obtained under the same conditions. As it is evident from 13C-NMR spectroscopy and GPC analysis the water soluble fraction from TMAHP-SWM consists only of lignin-saccharide degradation products. The NaOH extracts of TMAHP-SWM and TMAHP-holocellulose as well as the water-soluble fraction from TMAHP-holocellulose are polymeric materials. From TMAHP-SWM only 3.1% of alkali-soluble material could be extracted, while from TMAHP-holocellulose 15.7% of water-soluble and 7.9% of alkali-soluble materials were obtained.
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    Journal of Applied Polymer Science 33 (1987), S. 2707-2714 
    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: Grafting of the mixture of acrylamide and acrylic acid onto polyester and polypropylene fibers and mixture of acrylic acid and methacrylic acid onto polypropylene by the radiation method are reported. It is observed that when pure acrylamide was used for grafting, the grafting extent was small, whereas when the mixture was used, the amount of acrylamide content in the copolymer was found to be more than the feed ratios. The results are explained on the basis of chain transfer mechanism. With methacrylic acid and acrylic acid mixtures, the rate of grafting decreased with the increase in the concentration of acrylic acid in the feed ratio, and this has been explained on the basis of the formation of either a 3-dimensional network structure or a highly branched structure involving backbone polymer molecules with acrylic acid, which prevents the diffusion of the monomer from the solution phase to the swollen phase.
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    Notes: Cinnamoyloxymethyl dimethyl vinyl silane was synthesized and bound to a series of commercial polydimethylsiloxane-type copolymers bearing variable amounts of Si—H functions through a hydrosilylation reaction. This reaction was controlled in order to avoid side reactions between the photosensitive unsaturated moiety and the Si—H groups.The photosensitivity of polymeric films was studied by a photoresist test described in previous papers. The results emphasize the role of the molecular weight of the starting copolymer and the percentage of pendant photosensitive groups.
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    Journal of Applied Polymer Science 33 (1987), S. 2249-2252 
    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
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    Journal of Applied Polymer Science 33 (1987), S. 2253-2258 
    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
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    Journal of Applied Polymer Science 33 (1987), S. 1983-1991 
    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 melting temperatures (TM) of hydrogels prepared by chilling aqueous solutions of syndiotacticity-rich poly(vinyl alcohol) (s-PVA) at 0°C were measured rising temperature of gels from the initiative temperature (TI) of 0-70°C (every 10°C). The apparent enthalpies of fusion of a junction ΔH's were estimated from the relation between the logarithm of polymer concentration (log C) and 1/TM. ΔH depended on TI, showing that the melting point of gels depended on a thermal hysteresis. The highest polymer concentration CH in those of the gels which have no melting point above an initiative temperature was determined and ΔH was estimated from the relation between log CH and the reciprocal melting point of the gels with CH, 1/TIM. The ΔH was 15.1 kJ/mol in the range of higher polymer concentrations and 43.9 kJ/mol in the range of lower concentrations.
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    Journal of Applied Polymer Science 33 (1987), S. 2041-2052 
    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 pyrolysis and gaseous combustion of poly(ethylene terephthalate) (PET) incorporating poly(4-bromostyrene), poly(vinyl bromide), and poly(vinylidene bromide) has been studied using thermogravimetry, flammability limit evaluation, and hydrogen bromide (HBr) evolution techniques. The data obtained have been compared with limiting oxygen index (LOI) flammability data to elucidate flame retardation mechanisms. All the organo bromides studied (applied either via topical treatment or radiation grafting) released HBr on pyrolysis which is capable of inhibiting the gas phase combustion reactions. Condensed phase interactions were also detected which were capable of altering the gaseous pyrolysates. Thermal stability considerations suggest that, although the aliphatic bromides are excellent sources of HBr, they are not ideal flame retardants for PET.
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    Journal of Applied Polymer Science 33 (1987), S. 2077-2086 
    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 application of ultraviolet (UV)-curable polymeric coatings provides optical fibers with improved strength, microbending resistance, and long-term durability. To ensure constant optical properties of the glass fibers during their life, fully polymerized coatings are needed. Test methods capable of determining the degree of cure and the consistency of the polymeric materials used are therefore required by the fiber technology. This investigation deals with the description of a calorimetric test method for the direct determination of the prepolymer reactivity and its final degree of cure. The analytical technique uses a modified differential scanning calorimeter (DSC) capable of direct measurements of heat fluxes generated during the UV-activated polymerization of photoinitiated acrylic prepolymers. Finally, the degree of cure and the glass transition temperatures were determined for the polymerized coating also in presence of sorbed moisture.
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    Journal of Applied Polymer Science 33 (1987), S. 2087-2095 
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    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: Several antioxidants alone, and in combination with sulfonated UV absorbers, have been evaluated as photoprotective agents for wool. Mixtures of phenolic antioxidants and sulfonated UV absorbers of the 2-hydroxyphenylbenzotriazole class were found to exhibit synergistic behavior; the most effective UV absorber also gave the strongest synergistic effect with the antioxidants. Of the systems studied, the hindered phenol, calcium bis ((ethyl-(3,5-di-t-butyl-4-hydroxybenzyl)-phosphonate)) (Irganox 1425), when used in conjunction with a sterically hindered benzotriazolesulphonate, afforded wool the best protection against photoyellowing and phototendering in sunlight, behind window glass. Sulfonated derivatives of hindered phenols acted synergistically with UV absorbers when treated fabrics were exposed to an artificial light source, but not when fabrics were exposed to sunlight through glass.
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    Journal of Applied Polymer Science 33 (1987), S. 3019-3036 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The macroscopic order parameter S in the cholesteric liquid crystalline phase of hydroxypropyl cellulose (HPC) and ethyl cellulose (EC) solutions was calculated using refractive index data. Haller's extrapolation approach was used. The S calculated was compared with the S predicted from Doi's theory. The calculated values of S for HPC and EC solutions were in the range of 0.4-0.8 within our experimental range, and agreed with the predicted values of S obtained with Doi's theory. This result suggests that Haller's approach is valid for determining S for liquid crystalline solutions of HPC and EC, despite the scattering of the data at higher temperatures.
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    Journal of Applied Polymer Science 33 (1987), S. 3069-3079 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Some properties of the polyesters treated with such an addition-type chain extender as 2,2′-bis(2-oxazoline) (BOZ) have been investigated. The molecular size distribution and the melting point of the resultant polyesters indicate that BOZ reacts to form linear chain-extended polymers without branching. As for their thermal stabilities, unreacted oxazoline remained in the polymer can act as a heat stabilizer by further reacting with carboxyl terminals of the polymers and by preventing decrease in the molecular weight even in the solid state. On the other hand, BOZ unit incorporated in the polyester chain was relatively thermally unstable compared with the ordinary polyester chain, especially under the polyester melt condition. The polyester treated with BOZ has a rather low carboxyl content, and considerable improvement in the hydrolytic stability has been observed. But unreacted oxazoline groups adversely affected the hydrolytic stability, although the effect was about eight times as small as that of carboxyl groups.
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    Journal of Applied Polymer Science 33 (1987), S. 2263-2264 
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    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
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    Journal of Applied Polymer Science 33 (1987), S. 2267-2267 
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    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
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    Journal of Applied Polymer Science 33 (1987), S. 2353-2368 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The hydrodynamic degradation of high molecular weight poly(acrylamide-co-Na acrylate) in 1M NaCl in porous media flow was studied as a function of polymer concentration in the dilute and semidilute concentration ranges. Porous media rheometry was used to monitor molecular weight changes due to chain scission. At equivalent superficial velocities of flow through a glass bead pack, polymers at dilute concentrations showed greater loss of molecular weight than polymers at semidilute concentrations.
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    Notes: Polymer membranes having cationic charge site, poly(1-alkyl-4-vinylpyridinium iodide-co-acrylonitrile) (alkyl: methyl, butyl, or octyl) were prepared in terms of coulombic interaction for separation of water-ethanol mixtures. The incorporation of cationic charge site into the membrane led to improve not only separation factors (selectivity toward water) but also flux number in the separation of aqueous ethanol solution by pervaporation technique. Target values, which were requested to have from the viewpoint of industrial utilization for separation of aqueous ethanol solution were attained as follows: separation factor toward water over 50 and flux value over 500 g m-2 h-1, through poly(1-methyl-4-vinylpyridinium iodide-co-acrylonitrile) (membrane 3) (quarternized fraction of pyridinium moiety, 89.5%; mol fraction of pyridinium moiety, 0.034) and poly(1-butyl-4-vinylpyridinium iodide-co-acrylonitrile) (membrane 5) (quarternized fraction, 100%; mol fraction of pyridinium moiety, 0.038). It was found that the introduction of cationic charge site into the membrane was one of feasible methods to obtain suitable membranes for water permselective membranes in the separation of water-ethanol mixtures.
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    Journal of Applied Polymer Science 33 (1987), S. 2439-2447 
    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 change in attenuation of longitudinal ultrasonic waves has been measured as a function of frequency and temperature for natural rubber samples loaded with intermediate super abrasion furnace (ISAF) in increasing quantities and vulcanized with N-oxidiethylene benzotriazol sulfunamid (OBTS) after being subjected to natural aging for 5 years. Three relaxation processes, namely α, β, and γ, were noticed. The activation energy for each process was calculated and the results are discussed. Also, the dielectric constant ε′ and dielectric loss ε″ have been investigated for those samples after being immersed in various water media. The measurements were carried out in the frequency range from 100 Hz up to 100 kHz and at room temperature (∼ 28°C). The results are compared with each other and the differences are interpreted.
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    Journal of Applied Polymer Science 33 (1987), S. 2493-2501 
    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: Rheological and mechanical properties of polyvinyl chloride (PVC) compounds vary with the polymer entanglement state at the time of testing. Controlled shearing episodes and thermal histories applied to the compounds produce major property variations. These then relax toward steady-state values at rates which are consistent with diffusion-controlled processes, presumably connected with the development of steady-states in entanglement couplings. Activation energies of 4-7 kcal/mol apply to the proposed re-entanglement processes. Rates of property variation can be altered by the addition of fillers to the compounds, the interactions between polymer and filler being an important factor in this regard. CaCO3 samples with strong affinity for the PVC retard the rate of property variations (i.e., the filler tends to stabilize non-steady-state entanglement couplings). Fillers, surface treated so as not to interact strongly with the polymer, produce lesser effects on relaxation rates. The data indicate the feasibility of controlling both the sensitivity of polymer properties to processing variables, and the rates of property change associated with the attainment of steady-state polymer entanglement morphologies.
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    Journal of Applied Polymer Science 33 (1987), S. 2581-2586 
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    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
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    Journal of Applied Polymer Science 34 (1987), S. 377-393 
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    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: Small but significant numbers of chain scissions occur in a commercial poly(methyl methacrylate) sheet exposed to temperatures between 50 and 125°C. The scission rate is initially high and then levels off to a constant rate. The short-time rate of chain scissions is temperature dependent, while the long-time rate of chain scissions appears to be temperature independent. Four possible sources of random chain scission initiation were considered: (1) the presence of unreacted initiators of polymerization, (2) free radicals generated from additives in the commercial film, (3) weak links in the polymer chain, and (4) free radicals generated from the thermal decomposition of an oxidation product of methyl methacrylate (MMA) monomer. The source most consistent with our results is the one involving free radicals generated from the oxidation product of MMA monomer.
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    Journal of Applied Polymer Science 34 (1987), S. 409-422 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Areas under the linear tan δ-temperature (tA) and linear loss modulus-temperature (LA) curves of the polyacrylate and polymethacrylate homologous series and their interpenetrating polymer networks (IPNs) were investigated. For poly(methyl acrylate), LA values are independent of crosslinking level through 25%, but tA decreases. With increasing side group length, on the other hand, tA remains nearly independent of side group length for both homologous series, having values near 50 and 65 (units of K) for the acrylate and methacrylate series, respectively. However, LA decreases steeply with increasing side group length. A phenomenological treatment of areas is presented in order to explain tA and LA behavior semiquantitatively. Both tA and LA exhibit areas characteristic of the structure of the particular polymers. The homopolymer LA areas are additive in determining the area under the corresponding curve for the IPN. This suggested a group contribution analysis for LA, where each moiety contributes specific values to the area.
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    Journal of Applied Polymer Science 34 (1987), S. 537-548 
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    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: Ternary blends comprising bisphenol-A polycarbonate (PC), the polyhydroxyether of bisphenol-A (Phenoxy), and poly(ε-caprolactone) (PCL) were found to be generally miscible at PCL levels greater than 60% by weight and to show multiple amorphous phases at lower PCL levels. The melting point depression of PCL in the miscible region of the ternary and in the miscible binary blends with PC and Phenoxy was examined to obtain the enthalpic interaction parameters, Bij, for each of the three binary interactions. The parameters associated with the miscible binary blends were negative, as expected, and indicated that PCL interacts more exothermically with Phenoxy than with PC. The parameter associated with Phenoxy/PC interaction was strongly positive as expected from the complete immiscibility shown by these materials. The interaction parameters were used to calculate the locus of compositions for which the heat of mixing is zero. The locus was found to agree well with the observed boundary between miscible and multiphase behavior in the ternary. This suggests that the phase behavior of ternary blends is largely determined by the same enthalpic considerations known to govern the phase behavior of binary blends.
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    Journal of Applied Polymer Science 34 (1987), S. 593-599 
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    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: On heating in DSC, samples of UHMWPE show a single, fairly sharp, melting endotherm which may be increased to a peak temperature of 147°C and 77% crystallinity by annealing at elevated temperatures. An irreversible conversion of nascent to folded crystals, between 134 and 142°C, was observed by heating nascent UHMWPE powder in the calorimeter. In the presence of n-hexatriacontane, the melting endotherm of UHMWPE was depressed and broadened and the conversion of nascent to melt-crystallized polyethylene facilitated on heating. A melt-crystallized mixture of ordinary linear polyethylene (HDPE) and UHMWPE was not resolved on remelting. After annealing this mixture for 12 h at 130°C, HDPE was fractionated and the melting of UHMWPE was sharpened. Crystals of UHMWPE, prepared from dilute solution in xylene, show a single sharp melting endotherm and high crystallinity, but the melting peak is reduced in temperature compared to nascent crystallized powder.
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    Journal of Applied Polymer Science 34 (1987), S. 627-638 
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    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 nondestructive technique based on the photoelastic properties of transparent polymers has been used to monitor the distribution of residual stress components in circular rods of poly(methyl methacrylate) (PMMA). The influence of various thermal histories on these stresses as well as on the molecular birefringence has been determined. The technique has been further simplified to obtain the values of maximum tensile and compressive residual stresses with the help of just two photoelastic measurements. The stresses so obtained are within 10% of the values obtained using detailed experimental measurements and their analysis. The simplified procedure is, therefore, suitable for “on-line” determination of residual stresses in extrusion industry.
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    Journal of Applied Polymer Science 34 (1987), S. 657-676 
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    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 possibility of multiple steady states for a polymer particle is examined for propylene and ethylene, liquid and gas phase polymerizations. It is shown that multiple steady states should not occur in conventional diluent slurry polymerizations, but are always a possibility for gas phase and bulk propylene slurry reactions. Simulations to determine particle temperatures as a function of particle diameter show that polymer melting is predicted immediately upon catalyst injection for many cases in a gas phase reactor and for some cases in bulk polymerization. The practical implications of this result are discussed.
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    Journal of Applied Polymer Science 34 (1987), S. 721-735 
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Both the rate and apparent equilibrium of propane sorption in glassy polystyrene were increased after swelling the polymer by exposure to a highly sorbing vapor. Cyclic sorption experiments revealed that the increase in rate and apparent equilibrium of sorption due to the preswelling treatment decayed only during vacuum aging. The presence of low levels of propane in the polymer during aging, however, appeared to arrest the decay in sorption capacity. These composite results, taken in conjunction with the results of previous work in our laboratory, suggest that the component of the total sorption which resides in nonequilibrium, distended interchain gaps retards the chain motions which otherwise lead to consolidation of the dilated glass.
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    Journal of Applied Polymer Science 34 (1987), S. 737-741 
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    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: Graft copolymerization of methyl methacrylate initiated by ceric ion in aqueous medium on bleached holocellulose was studied at 29°C. It was found that an increase in the concentration of ceric ion and oxidation of the holocellulose with aqueous potassium dichromate solution resulted in increased levels of incorporation of poly(methyl methacrylate) graft copolymer, but were associated with reductions in the efficiency of grafting. Thiol groups were introduced on the holocellulose by treatment with dilute thioglycollic acid solutions at 29°C. The influence on the level of grafting and on the molecular weight of the grafted polymer by the incorporated thiol groups on the substrate was examined.
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    Notes: Based on reactivity ratios reported earlier, a number of copolymers of methyl methacrylate and tri-n-butyltin methacrylate has been prepared. Release of tri-n-butyltin oxide into seawater from the copolymer films has been determined at 30°C as a function of time. The copolymers behave in a typical manner - an initial increase in leaching rate followed by a steady state which is reached after about 60 days. Pigmented copolymer films behave in a similar manner, even though the overall leaching rate is slightly lower. Release rate data are also presented for a typical antifouling paint formulation.
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    Journal of Applied Polymer Science 34 (1987), S. 829-845 
    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 mathematical model which describes conversion and molecular weight development in the homogeneous polymerization of butadiene has been developed. The reaction scheme and derivation of the model equations are included. It was found that a catalyst formation efficiency must be estimated for each polymerization. The correct trends were predicted, although weight-average molecular weight was often underestimated. The model could not fully account for the effect of water concentration.
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    Journal of Applied Polymer Science 34 (1987), S. 881-886 
    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
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  • 80
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: Pure regenerated cellulose fibers and those containing various amounts of phosphorus nitride were pyrolyzed under different conditions in the temperature range of 150-440°C. Easily volatile liquid pyrolysis products, the tar fraction of limited volatility, and the charred residue were determined gravimetrically. The liquid volatiles were analyzed by combined gas chromatography/mass spectrometry for their water content. The tarnfraction and the charred residue were inspected by infrared (IR) spectroscopy. The studies revealed that the phosphorus nitride flame retardant enhances the onset of the pyrolytic decomposition and the release of water at substantially lower temperatures as observed for pure cellulose. The water release favors the carbonization and its extent reduces the formation of levoglucosan as a precursor of easily flammable pyrolysis products. Thus phosphorous nitride must be classified into the water release favoring flame retardants.
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  • 81
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    Notes: Two latex interpenetrating polymer networks, one based on a partially compatible pair and the other based on an incompatible pair of polymers, were prepared by a two-stage emulsion polymerization. To investigate the effect of swelling the first formed polymer particles with the second monomer, the second stage of the synthesis was conducted after allowing the second monomer to be in contact with the seed latex for specified periods of time. Fabricated samples of these interpenetrating polymer networks were subjected to hardness, stress-strain, and dynamic mechanical measurements. The results showed an enhancement in mixing of the two networks in the case of the partially compatible pair and a detectable increase in the level of mixing for the incompatible pair.
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  • 82
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    Journal of Applied Polymer Science 34 (1987), S. 527-536 
    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: Analysis of sequence distribution (SD) in poly(vinyl alcohol-co-vinyl acetate) (p(VA-VAc)) by the iodine complexation method (ICM) was investigated through the formation of a red complex of p(VA-VAc) with iodine-iodide. Differential thermal analysis (DTA) has been known to be a measure of SD and the ICM was also suggested to be valid for the SD analysis. ICM can be applied for samples of p(VA-VAc) rich in VAc-unit content, in which DTA could not be used. Results of SD analysis on p(VA-VAc) by 1 NMR spectra were compared with those from ICM, and excellent agreement was found between data. The ICM can be applied as a convenient screening method for SD of p(VA-VAc) as far as the red-complex formation is concerned, and was shown to have much wider applicable range than the DTA method.
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  • 83
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    Journal of Applied Polymer Science 34 (1987), S. 587-592 
    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 concentration dependence of solvent self-diffusion coefficients is examined near the pure solvent limit. It is shown that it is possible to explain an apparently anomalous concentration dependence for the solvent self-diffusion coefficient at high penetrant mass fractions within the framework of the free-volume theory of transport.
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  • 84
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    Journal of Applied Polymer Science 34 (1987), S. 601-616 
    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 series of bisphenol A dicyanate network polymers with degree of crosslinking varied by addition of 4-cumylphenylcyanate were prepared and characterized by model compound study, infrared spectroscopy, DSC, TGA, and statistical analysis. Laser ablation energy measurements varied from 14 to 18 kJ/g and were found to linearly increase with degree of crosslinking. Comparative ablation energy analysis was made with other aromatic, nonaromatic, linear, and crosslinked polymers.
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  • 85
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    Journal of Applied Polymer Science 34 (1987), S. 617-625 
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    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: Effects of rheological parameters of polyolefin suspension were studied to better understand stirred tank polymerization reactors and their engineering principles. Experimental results have been fitted into a quadratic model. Consistency index and behavior index have been determined as functions of solids concentration, temperature, and particle size.
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  • 86
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    Journal of Applied Polymer Science 34 (1987), S. 677-687 
    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
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  • 87
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    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Bead-shaped, divinylbenzene-cross-linked terpolymers, consisting of hemin (ferri-protoporphyrin IX chloride), styrene, and 2-methyl-5-vinylpyridine, were prepared by suspension polymerization in which all or part of styrene monomer was replaced with divinylbenzene. Analogous terpolymers of the cross-linked and uncross-linked formless types were also prepared by solution polymerization. All the terpolymers obtained were characterized by electron spin resonanance spectroscopy, scanning electron microscopy, and measurement of specific surface area. The characteristic of the adsorption of cyanide ion onto the terpolymer beads was investigated and compared with those adsorbed onto their analogs. The column separation of cyanide ion with the terpolymer beads was carried out to examine the ion-adsorbing capacity. It was found that the suspension polymerization is just appropriate to prepare a cyanide ion exchanger in the form of beads.
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  • 88
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    Journal of Applied Polymer Science 34 (1987), S. 559-569 
    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 effects of composition, molecular weight, and milling temperature on homogeneity, gas permeability, selectivity of oxygen/nitrogen, and mechanical strength of the TPX/siloxane blend membranes were studied. By adjusting the blending conditions and hence controlling the homogeneity, the gas permeability of TPX membrane was significantly improved without loss of oxygen/nitrogen selectivity. The oxygen permeability of 1.57 × 10-8 cm3 (STP) cm/cm2 s cm Hg and the oxygen/nitrogen permeation ratio of 6.92 can be obtained under the condition of TPX (MX-001)/siloxane (75,000 MW) = 9/1 at 65°C milling temperature. This membrane possesses 133 kg/cm2 tensile strength and 92% elongation. The morphology of the blend membranes was studied.
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  • 89
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    Keywords: Chemistry ; Polymer and Materials Science
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    Notes: Observations and conclusions drawn from a model N-methylol reactant system have been used to study formaldehyde release from cotton fabric treated with N,N′-dimethylol-4,5-dihydroxy-ethyleneurea (DMDHEU). Reagent residues produced by DMDHEU in the presence of sodium bisulfate or zinc nitrate were found to be more complex than those formed from the N-methylolpyrrolidone (NMP) reactant system, and the exact nature of some of the residues from DMDHEU could not be established. Zinc nitrate produces higher fixation of DMDHEU on cotton as compared to sodium bisulfate and also reduces formaldehyde release. As is the case with the NMP system, the lower amount of formaldehyde release with zinc nitrate catalyst is believed to be at least partially due to the formation of a complex between the N-methylol reactant, DMDHEU, and zinc nitrate. The C—OCell bonds in both finishes resist acid-catalyzed cleavage but cleavage of the N—C bonds in N-methylol groups (to release formadehyde) in the presence of acid is greater for the DMDHEU system than for the NMP system. Results with the DMDHEU and NMP systems are similar, but because of the complex nature of the products formed in the DMDHEU system it is very difficult to correlated formaldehyde release with specific chemical structures of residues or reactants.
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  • 90
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    Journal of Applied Polymer Science 34 (1987), S. 571-585 
    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 differential equations governing the molecular weight distribution (MWD) in step-growth polymerization are coupled and nonlinear and a large number of them must be solved simultaneously to keep the truncation error low. In this work, these equations have been decoupled so that they can be solved sequentially. The solution of these is independent of the truncation error and there is considerable saving of computation time. To demonstrate the efficiency of the algorithm, the formation of polyethylene terephthalate (PET) in batch reactors with ethylene glycol evaporating has been analyzed. The feed to the reactor is taken as polymer with its oligomers present according to the Flory's distribution. The effect of pressure and temperature of the reactor on the progress of polymerization has been modelled and evaluated. The amount of ethylene glycol distilled, the concentrations of the first five oligomers Q1 to Q5, the number average chain length, and the polydispersity index of the polymer have been determined. It is shown that the reduced pressure and increased temperature reduce the concentration of the condensation product in the reaction mass, thus pushing the polymerization in the forward direction. Lastly the CPU time on Dec 1090 using this algorithm is only 0.40 s compared to about 10 min for similar computations using other existing methods.
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  • 91
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    Journal of Applied Polymer Science 34 (1987), S. 1037-1056 
    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: Gas transport properties in homogeneous blends of PMMA with each of two SAN random copolymers, containing 13.5 and 28% by weight of acrylonitrile respectively, have been measured at 35°C for He, H2, O2, N2, Ar, CH4, and CO2. For all cases, the permeability and diffusion coefficients are higher than that expected from the semilogarthmic additivity rule. On the other hand, the solubility coefficients and the ideal gas separation factors follow this rule well. These results for PMMA/SAN blends differ from those observed recently for other miscible blend systems; however, they agree well with recent theories proposed to describe gas sorption and permeation behavior in polymer mixtures. The composition dependence of gas transport properties observed in PMMA/SAN blends is attributed to the very weak net interactions between PMMA and SAN produced by repulsions between styrene and acrylonitrile units in the SAN random copolymers. Gas transport properties in phase-separated PMMA/SAN blends have also been studied. The phase-separated blends show sorption and permeation properties very similar to the corresponding homogeneous blends which can be explained by an isotropic, interconnected, two-phase model proposed by Kraus and Rollmann. Gas permeabilities for the solution cast PMMA films used here are compared with melt-extruded specimens used previously, and the differences are attributed to molecular orientation.
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  • 92
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    Journal of Applied Polymer Science 34 (1987), S. 1093-1108 
    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: It is well known that cation exchange membranes, having a very thin layer of a cationic polyelectrolyte on the membrane surface, have preferential permselectivity for monovalent cations in a monovelent-divalent cations system. We studied the relationship between preferential permselectivity and molecular structure of the cationic polyelectrolyte. Grafted poly(4-vinyl-N-methylpyridinium-iodide) was used and was compared with poly(4-vinyl-N-methylpyridiniumiodide). The backbone polymers were poly(styrene-co-p-benzylstyrene) and poly(benzyl), onto which 4-vinylpyridine was grafted by anionic polymerization and then quaternized with CH3I. The grafted poly(4-vinyl-N-methylpyridinium-iodide) is effective in making the cation exchange membrane preferentially permselevtive for Na+ - Ca2+ system and is more preferable than poly(4-vinyl-N-methylpyridinium-iodide) in terms of electric resistance of the membrane. However, the relationship between the molecular structure of the cationic polyelectrolyte and the durability of the preferential permselectivity is not clear.
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  • 93
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    Notes: Lignocellulose materials were modified with 3-chlor-2-hydroxypropyltrimethylammoniumchloride, 1,3-bis(3-chlor-2-hydroxypropyl)imidazoliumhydrogensulphate, and 2-chlorethyl-sodiumsulphonate and the flame-retardant properties of materials obtained were studied. The flame-retardant effect was proved using the limited oxygen index (LOI) method and values up to 32.8 vol % of oxygen were determined. The LOI values were higher when the modification was done without using NaOH for activation, but in that case the alkylating groups were not chemically bonded to the material. The NaOH activation was necessary to obtain material with flame-retardant properties stable against washing. No synergistic effects were observed when the material was modified with both nitrogen- and sulfur-containing groups.
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  • 94
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    Journal of Applied Polymer Science 34 (1987), S. 1145-1157 
    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 combination of the laser and optical diffraction analysis provides a powerful tool for the determination of fiber orientation distribution in any paper sheet of basis weight low enough to be translucent to the laser beam. The coherent light beam from the laser is diffracted by the sample. It undergoes a Fourier transform from which the orientation distributions can be calculated. Measurements were made on 14 different samples of various degrees of orientation, including an essentially random handsheet as a control. The cross-direction/machine direction elastic modulus ratios of the samples were found to correlate well with the distribution functions fitted to the orientation data. The correlation curve was S-shaped, with a drastic drop in the modulus ration in the medium range of fiber orientation.
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  • 95
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    Journal of Applied Polymer Science 34 (1987), S. 1199-1208 
    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 new technique of derivative infrared spectroscopy for the study of polymer structure with special reference to cotton cellulose is described. Absorption spectra of cotton cellulose are compared with second deravative spectra. In case of absorption spectra, while determining the wavelength and intensity of a given absorption, in many cases, difficulties arise due to the presence of an interfering band which, as a consequence of overlap, prevents the determination of the above properties. Derivative spectroscopy provides valuable information on structural properties of cellulose. It yields spectra gradient, which facilitates the separation of overlapping absorption bands to resolve and detect absorptions; neither were unresolvable as a consequence either of multiple bands overlap or of low intensity. Hence, the measured wavelength in the second derivative spectra are more precise than the absorption spectra. For fine structural studies of cellulose, derivative spectra may provide more useful information as the absorption bands are more clearly defined.
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  • 96
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    Journal of Applied Polymer Science 34 (1987), S. 1217-1234 
    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 viscoelastic properties of cellulose acylates, its mixed acylates, and (cellulose oligo-oxymethylene ether) acylates (COM acylates) have been meausured in the molten state over wide ranges of frequency and temperature. The log G′ vs. log ω curves as well as the similar curves for the loss modulus G′ at various temperatures for cellulose acylates could not be superposed into respective master curves by use of the time-temperature superposition principle. This is considered to be caused from the orientation of cellulose acylates main chain in the molten state. In the case of cellulose mixed acylates, rheological simplicity was found but this was only the case on selected combinations of acyl groups. Most cellulose acylates, which were introduced oxymethylene chains (OM chains) in between glucopyranose ring and the acyl group, behaved as thermorheologically simple materials in the molten state. When the acyl groups become large, however, it is necessary to introduce long OM chains in order to get thermorheologically simple COM acylates in their molten state. Several studies have been made concerning the behavior of side chains, both the OM and the acyl chains, of COM acylates in the molten state.
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  • 97
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    Journal of Applied Polymer Science 34 (1987), S. 1285-1300 
    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: An investigation has been made into the mechanism of cold drawing in melt-spun poly(ethylene terephthalate) (PET) fibers. An analysis of the cold-drawing behavior using wide-angle x-ray diffraction, orientation measurements, calorimetric and mechanical techniques was performed. The evidence suggests that the cold-drawing process involes stress-enhanced crystallization which occurs in conjuction with incresing orientation of the crystalline and amorphous regions. A degradation in the fiber properties after cold drawing was observed for fibers spun below 1,000 m/min while fibers spun above 1,000 m/min exhibited an improvement in fiber properties with cold drawing. This behavior was explained by the existence of two distinct irreversible deformation micromechanisms for fibers spun below and above 1,000 m/min.
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    Journal of Applied Polymer Science 34 (1987), S. 1325-1327 
    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
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    Journal of Applied Polymer Science 34 (1987), S. 1335-1343 
    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 rheological behavior of high density polyethylenes with very broad molecular weight distribution is studied in the molten state starting from freshly synthesized powders. The complex viscosity increases slowly up to a limiting value as a function of ageing of the polymer and faster when the molten polymer is stirred. The phenomena are explained by an heterogeneous distribution of very high molecular weight nodules in the polymer arising from the synthesis and is proved by the preparation and characterization of polymers presenting the opposite heterogeneity and behavior (very low molecular weight nodules).
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    Journal of Applied Polymer Science 34 (1987), S. 1367-1382 
    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 comprehensive kinetic model using the functional group approach has been proposed for the polymerization of melamine and formaldehyde. The kinetic model is consistent with the basic chemistry of polymerization and involves five rate constants which have been estimated using the experimental data of Tomita. Homogeneous continuous-flow stirred-tank reactors (HCSTRs) have been modelled and the mole balance relations for various functional groups have been written. The performance of HCSTRs is governed by algebraic equations and, for any specified residence time, is found by the method of successive substitution using the Brown's algorithm. The computations show that as long as free formaldehyde is present, the reaction mass would consist predominantly of substituted melamine molecules. However, after formaldehyde is completely reacted, larger oligomers are formed in larger concentrations. On comparison of results with batch reactors, it is found that for the same reaction time HCSTRs yield polymer with higher branching.
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