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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985) 
    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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  • 2
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 36-36 
    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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  • 3
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 332-338 
    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 step growth polymerization of RAf type multifunctional monomers (with A reacting with A) in cascades of isothermal, homogeneous, continuous flow stirred tank reactors (HCSTR's) is simulated. It is found that our equations reduce to those of Cozewith, et al. If either f or the molecular weights are large. However, under certain conditions, the low molecular weight correction is significant and the more exact equations of the present work must be used. Several possible start-up strategies are discussed, of which one is amenable to analytical solution. This is the one in which all HCSTR's are filled initially with the steady state feed from the previous reactor and the outputs from any reactor, during its start-up period, are discarded to an ‘off spec’ tank. It is found that for this case, in order to ensure nongelling operation, the mean residence time of any HCSTR must lie below a certain critical value, depending on the value of f and the feed conditions.
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  • 4
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 339-347 
    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: Measurements of the resistance force to a wide range of contact loadings have been performed on poly(methylmethacrylate), polycarbonate, and epoxy specimens. Rigid spherical indenters of 4.5, 9, and 18 mm diameter, as well as cones of various apex angles, were driven into thick specimens at constant velocity over the range 0.005 to 150000 mm/min. The objective of this study was to develop a data base useful for the understanding and analysis of the phenomena involved when polymeric solids are impacted by small hard bodies. Spheres and cones were used because these symmetrical shapes offer the best chance for analysis in terms of viscoelastic extensions of the classical Hertz elastic contact problem. Measurements covered penetration depths from first detection of contact, where the strains are smallest and the material response should most likely be interpretable in terms of linear viscoelastic analysis, to much greater depths where the strains far exceed the yield values. The observations are tabulated, as are the values of parameters that allow the data to be modeled to within experimental error. These parameters fit into a specially developed empirical law designed to facilitate subsequent treatment of the data using Laplace transform methods. An analysis is offered to try to sort out time-dependent force relaxation from depth-dependent force increase during the progress of the penetration. The results of the response at small penetration depths are in broad accord with published relaxation moduli. However, the dependence of force upon indenter geometry does not follow simple expectation.
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  • 5
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 377-388 
    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: Morphological studies have been carried out on a thermotropic liquid crystalline copolyester based on poly(ethylene terephthalate) (PET) and para hydroxybenzoate (PHB) that has been subjected to different types of flow histories. Wide angle X-ray scattering investigations and chemical etching (n-propylamine is the etchant) in conjunction with electron microscopy studies conducted on end gated injection molded plaques of the 60 percent PHB and 80 percent PHB copolyesters indicate that a highly oriented skin region and a less oriented core region is present. Chemical etching studies performed on microtomed layers of end gated and center gated plaques show that the etching is less pronounced in the skin region and is more pronounced in the core. The microtomed layers of the end gated injection molded plaques when analyzed by ESCA indicate the presence of a “PHB rich” skin region and a “PET” rich core region. Biaxial orientation, as denoted by WAXS measurements, is observed when the 60 percent PHB copolyester is squeezed between lubricated parallel plates.
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  • 6
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 406-411 
    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: Test results are presented for a matrix type phase change thermal storage tile module with no surface covering, intended to transfer heat directly to and from room air at small temperature differences. Heat is stored and released by melting and freezing mixtures of fatty acids, which constitute up to half the weight of the tile. The polymeric matrices tested were powders or granules of poly(vinyl chloride) (PVC), poly (vinyl acetate) (PVAc), poly(vinyl alcohol) (PVA), vinyl acetate-vinyl chloride copolymer (VAc-VC), and high density polyethylene (HDPE). The tiles keep their shape and dimensions without any weeping of liquid fatty acid, up to 37 or 51°C, depending on their composition. In the case of PVC and PVA, infrared spectra and differential scanning calorimetry indicate interactions between the polymer and the fatty acids, which may increase the surface tension and allow larger matrix pores before weeping begins. Some of the tiles were reinforced with glass fibers, and others with cellulose fibers. The best mechanical properties were obtained with 5 percent of long (85 to110 mm) glass fibers. Paraffin chloride and antimony trioxide served as satisfactory fire retardants.
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  • 7
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 37-47 
    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 simulation of tubular, high-pressure low-density polyethylene reactors is performed using a comprehensive kinetic scheme which includes branching reactions as well as reactions leading to vinyl and vinylidene group formation. The variation of the physical properties of the reaction mass with position has been accounted for. In addition to predicting the conversions of the monomer and initiator, the temperature, and the number-average molecular weight, this study enables the computation of the polydispersity index and the concentration of vinyl, vinylidene, and methyl groups as a function of position. These have important implications in terms of product properties. Detailed simulations have shown that the steady-state approximation can be used for obtaining the concentrations of the initiator and the polymer radicals. In addition, some simple closure conditions have been established. The effect of multiple intermediate feeds is also investigated and it is found that under certain operating conditions the reactor performance becomes inherently unstable.
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  • 8
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985) 
    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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  • 9
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 75-82 
    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 semiquantitative bubble formation mechanism is presented for the baking of polymer films, utilizing poly(methyl methacrylate) (PMMA)-ethyl acetate (EA) solutions as the model system. It is shown that bubble growth phenomena can he accounted for in terms of the competition between vapor pressure buildup and the rate of vapor dissolution. According to the proposed mechanism, the local pressure buildup of solvent in the polymer film is controlled by the solvent partial pressure above a solution having a planar interface at the corresponding temperature and solvent concentration. This pressure can he estimated by Raoult's law. The vapor dissolution rate, on the other hand, is dominated by the liquid-phase diffusion of the solvent. A method of obtaining the diffusion coefficient as a function of temperature and solvent concentration from isothermal thermogravimetric analysis (TGA) is also given.
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  • 10
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 98-104 
    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 subject of crazing in crystalline polymers is reviewed and specific consideration given to crazing in polypropylene (PP). Tensile tests conducted over a wide spectrum of temperatures and strain rates indicate that, for a given test temperature, there exists a critical strain rate above which crazing is the dominant deformation mode of PP. Similarly, for a given strain rate, there exists a critical temperature which demarcates crazing from shear yielding as the characteristic process of deformation. High deformation rates and low temperatures favor crazing, while low rates and high temperatures favor shear yielding. Crazes in crystalline PP were found to be morphologically similar to those in glassy polymers: high reflectivity, large area-to-thickness ratio, and planarity. They have a higher tendency to bifurcate than those in glassy polymers. Two types of craze fibrils could be identified: those parallel to σ11, and the randomly oriented interconnecting fibrils. It is demonstrated that microtome-trimming at low temperature followed by suitable chemical treatment is an effective technique of sample preparation for SEM examination of craze morphology in crystalline polymers. Further evidence has been provided that crazes in spherulitic polymers do not in general follow an interspherulitie path, but propagate through spherulites. The length of a craze in PP is not restricted to one spherulite diameter, nor does it grow radially.
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  • 11
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 113-117 
    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: Random multiblock copolymers of bisphenol-A-polycarbonate and poly(dimethylsiloxane) were hot-pressed or solvent cast into films which were studied by dynamic mechanical methods over the range 11 to 110 hertz (Hz) and 100 to more than 2200 Hz, respectively. The samples were studied also by differential-scanning calorimetry. The two phases are separated well in spite of the low-molecular weights of the blocks. This separation is altered by thermal history and by the solvent medium when solvent casting is used to prepare the films. The damping properties do not vary greatly with frequency. Damping is greatest near the glass-transition temperatures of the two components. The expansion of the block copolymer with heat appears to be retarded by the polycarbonate phase until the glass transition of that phase is approached.
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  • 12
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 129-156 
    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 singular class of polymer reactions can be caused by mechanical stress. Sufficient storage of mechanical energy to break chemical bonds in the main chain is generally possible only on deformation of polymers of high molecular weight. The corresponding appropriate conditions of high stress may occur in both polymer processing and use. This review summarizes reports of such polymer stress reactions published principally after 1980. The survey is organized by polymer type and by analysis technique.
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  • 13
    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: Blends of polyarylate (PA)-a copolyester of bisphenol A with a mixture of terephthalic/isophthalic acids at 50/50 proportion-and polycarbonate of bisphenol A (PC) were melt mixed into films with a Brabender Plasticorder. The processing produced transreacted mixtures that exhibited a modulus and yield stress with a maximum that is above the linear (very similar to that observed for compatible polymer blends). The elongation at yield did not show any maximum but it is also above linearity.
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  • 14
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 585-588 
    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: Deterministic mathematical models of the Maddock melting mechanism based on analytical and finite-difference solution methods are surveyed and classified according to the key assumptions involved. It has been concluded that the rigid solid bed concept coupled with a consistent non-Newtonian analysis of the melt flow pattern, including cross-channel circulation, leads to superior results. It is suggested that the development of the melting theory for the Maddock mechanism as an engineering analytical tool is virtually complete.
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  • 15
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 264-270 
    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: In an attempt to further understand the flow of polymeric melts through gates in injection molding, the present investigation deals with measurement of pressure drops during isothermal extrusion of fiber-filled and unfilled polystyrene, polypropylene, and polycarbonate melts in short tubes with sudden contraction at high shear rates typical of injection molding. Flow curves for these materials have been determined over a wide range of shear rates at various temperatures by using a capillary rheometer and extruder. Measurements indicate that rheological properties of fiber-filled melts after injection molding differ from those of fresh samples. Moreover, it has been found that decreasing the tube length increases the slope of the curve for pressure drop vs. Volumetric flow rate. Extra pressure losses due to end effects have been determined which show that at high shear rates these losses can reach levels as high as 100 bar, with the effect being higher for the fiber-filled melts. By using a viscoelastic consitutive equation, the extra pressure losses have been separated into entrance and exit losses. Model parameters required for this calculation have been determined from viscosity-shear rate curves for the melts. For various polymers, master curves useful for industrial applications have been constructed for the extra pressure losses.
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  • 16
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 517-520 
    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: Interpenetrating polymer networks (IPN's) can be defined as a combination of two polymers in network form, at least one of which was synthesized and/or crosslinked in the immediate presence of the other. Historically, the science of IPN's began with the papers of J. R. Millar in 1960 on homo-IPN's made from polystyrene, but the first recorded publication is a patent by J. W. Aylsworth in 1914. This latter system was based on phenol-formaldehyde for one network, and sulfur cured natural rubber for the other network. Early academic laboratories interested in IPN's include the Frisch team at Detroit and SUNY, who soon added their former student, Danny Klempner, and Yuri Lipatov's team at the Ukranian SSR Academy of Sciences in the USSR, as well as the author's laboratory. More recent academic teams interested in IPN's include Douglas Hourston at the University of Lancaster, England; Robert Cohen at MIT; S. C. Kim at the Korea Advanced Institute of Science and Technology, Seoul, Korea; G. Meyer and J. M. Widmaier in Strasbourg, France; and many others. Numerous industrial laboratories are interested, noting that about 90 U.S. patients have been granted, most of them in the past ten years. Systems of special interest include the new thermoplastic IPN's, which are really hybrid materials between polymer blends and IPN's, and the IPN-based RIM (reaction injection molding) materials. Other materials include the sequential IPN's and the SIN's, which have both polymers simultaneously polymerized, and the latex IPN's, which often exhibit core-shell characteristics.
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  • 17
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 553-561 
    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: Polymer blends of thermosetting and thermoplastic polymers were developed by properly mixing them in the presence of compatibilizers. Two compatibilizers that are structurally and chemically similar to thermosetting and thermoplastic polymers and a compatibilizer that does not have such similarity were synthesized. Polymer blends of phenol formaldehydepoly(methyl methacrylate) and phenol formaldehyde-polystyrene were prepared by using the compatibilizers, poly(phenol formal dehyde-s-triazine-methyl methacrylate), P(PF-g-MMA), poly(phenol formaldehyde-s-triazine-styrene), P(PF-g-S), and poly (cinnamaldehyde-co-oxy propylene oxy isophthaloyl-cooxy propylene oxy fumaroyl), P(C-g-E). The effects of molecular weight and quantity of the copolymer on the compatibility of the polymer were examined. The optimum compatibility which leads to superior tensile properties of the present blends was observed with P(PF-g-MMA) and P(PF-g-S) copolymers. The superior properties were also found to occur only in the range of the optimum molecular weight and quantity of the copolymer present in the blend. The polymer blends were analyzed by differential scanning calorimetry (DSC) and Electron Microscopy. DSC scans of P(PF-g-MMA) and P(PF-g-S) copolymer blends showed a single Tg whereas the scans of P(Cg-E) copolymer blends showed an additional Tg for unblended thermoplastic fractions. The electron microscopy studies also revealed good compatibility in P(PF-g-MMA) and P(PF-g-S) copolymer blends in which the unblended thermoplastic fractions are negligibly less. The UV-vacuum and heat resistance of the P(PF-g-MMA) and P(PF-g-S) copolymer blends were found to be good.
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  • 18
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    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 824-827 
    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: Sequential interpenetrating networks (IPN's) were obtained from a tetrafunctionally end-linked network [prepared from hydroxyl-terminated poly(dimethylsiloxane) (PDMS) chains having a number-average molecular weight of 21.3 × 103 g mol-1] by swelling it with very short vinyl-terminated PDMS chains (∼450 g mol-1), which were then themselves tetrafunctionally end linked, Simultaneous IPN's were prepared from a mixture of the same two types of PDMS chains, with different end-linking agents and catalysts for the two separate reactions. In elongation studies, both types of IPN's showed upturns in modulus which were similar to those shown by the usual bimodal networks, which are prepared from mixtures of chains having identical end groups, and are thus entirely interconnected. The sequential IPN's have values of the high deformation modulus close to those of the interconnected networks, possibly because their lack of connectivity is compensated for by the stretching of the long chains by the short-chains used to form the second network, Values of the ultimate strength are smaller for the IPN's, thus demonstrating the advantage of direct bonding between the long and short network chains. The simultaneous IPN's, however, have unusually large extensibilities, which makes their energies for rupture comparable to those of the corresponding interconnected bimodal networks.
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  • 19
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    Polymer Engineering and Science 25 (1985), S. 896-902 
    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: Mixtures of 90, 80, and 70 percent by weight bisphenol-A-polycarbonate (PC) and 10, 20, and 30 percent by weight styrene maleic anhydride (SMA) copolymer were melt-blended in a single screw extruder. Differential scanning calorimetry (DCS) and scanning electron microscopy (SEM) were used to determine the miscibility of the blends. The viscosity, as a function of shear rate and temperature, was measured by an Instron capillary viscometer. The notched impact strength as a function of temperature was measured by an Izod impact tester.The results of DSC showed two glass transition temperatures which merged slightly towards each other, indicating marginal miscibility of these blends. There was a decrease in viscosity as the fraction of SMA copolymer was increased. The most significant decrease occurred with the initial addition of SMA copolymer. The viscosity also decreased with increases in temperature. The impact strength of the blends was also dependent on SMA copolymer content. The blends showed six to ten times lower impact strengths at room temperature than the 100 percent polycarbonate. SEM analysis helped to determine the reason why the impact strength was lower for the blends. High magnification showed the presence of SMA copolymer inclusions dispersed throughout the PC matrix. These inclusions, which increased in size as SMA copolymer content was increased, acted as defects in the system.
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  • 20
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    Polymer Engineering and Science 25 (1985), S. 903-908 
    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 impact response of a glass fiber reinforced polypropylene was studied in a 3-point drop-weight impact test between -15 and 85°C and at a constant impact velocity of 2.2 m/s (5 mph). The response is a combination of tension and shear and can be expressed in terms of an apparent modulus, EA: 1 \documentclass{article}\pagestyle{empty}\begin{document}$$\frac{1}{{E_A }} = \frac{1}{{E_{11} }} + \frac{6}{{5G_{12} }}\left({\frac{d}{l}} \right)^2$$\end{document}.Where E11 is the tensile modulus, G12: shear modulus, d: specimen thickness, and l: specimen length.For a 40 weight-percent glass reinforced polypropylene, E11 was found to have a room temperature value of 5.8 GPa, and shear modulus of 0.43 GPa. Both decreased with temperature increase, with the shear modulus showing greater sensitivity to a temperature change. The fracture initiation and propagation energies were relatively independent of temperature. The fracture initiation energy per unit deformed volume was of the order of 1 MJ/m3. The total fracture energy was found to be sensitive to l/d: about 7 MJ/m3 at l/d of 5.3 and about 1.7 MJ/ m3 at l/d of 16.
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  • 21
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    Polymer Engineering and Science 25 (1985), S. 942-946 
    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 new rapidly crystallizing aromatic-aliphatic polyamide has been developed by reacting 4,4′-methylene bis(phenylisocyanate) (MDI) with aliphatic dicarboxylic acids. The polymer has a Tg of 130°C and Tm, of 290°C. Glass reinforced resin shows better flexural creep resistance at high stress levels (3000 psi) at elevated temperatures (75°C) than most reinforced semicrystalline commercial polymers i.e., nylons, thermoplastic polyesters and acetal because of its high Tg. Glass reinforced polyamide can be injection molded on conventional equipment to afford flexural moduli in excess of 1,000,000 psi and HDT's as high as 250°C at 264 psi. Because of the high level of crystallinity these parts will not dissolve or swell in most organic solvents and this aromatic aliphatic polyamide is also far less sensitive to moisture than commercial nylons.
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  • 22
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    Polymer Engineering and Science 25 (1985), S. 968-979 
    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: Capillary flow studies on bulk molding compound (BMC) using an instrumented injection-molding machine are reported. The significance of extensional flow effects with fiber-reinforced materials is emphasized. The extensional flow behavior in converging dies is modeled, and a means of evaluating both extensional and shear viscosity from capillary flow data is proposed. Methods of correcting results for the effect of deformation heating are discussed. The shear and extensional flow behavior of BMC in the temperature region 18 to 58°C can be fitted to a simplified Arrhenius Law.
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  • 23
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    Polymer Engineering and Science 25 (1985), S. 1001-1007 
    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 systematic study of wall effects on the shear viscosity of short glass fiber-filled polypropylene and polystyrene is presented. The dependence of these effects on capillary radius, shear rate, temperature, and polymer matrix is examined. The “true” viscosity curves of these materials (free from wall effects) can be obtained by an extrapolation procedure. Breakage of glass fibers in the high shear-rate processes of extrusion and injection molding lead to an appreciable reduction of the viscosity of these materials and is probably the more important effect to take into account in these processes.
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  • 24
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    Polymer Engineering and Science 25 (1985), S. 1026-1034 
    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: This review is mainly concerned with the conformational changes that depend on the dielectric constants for solvents for chlorinated polybutadienes (Cl-PBD) and their model compounds. The conformational equilibria of the rotational isomers of both meso and racemie 2,3-dichlorobutanes and 3,4-dichlorohexanes as the model compounds are discussed by analyzing infrared and NMR spectra. The solvent effect on the conformational parameter in Cl-PBD is explained by the variation in the conformation of the chlorinated part having polar C-Cl bonds. The matrix method is also described to calculate the temperature and solvent dependences of conformer populations.
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    Polymer Engineering and Science 25 (1985), S. 1055-1055 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 26
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    Polymer Engineering and Science 25 (1985), S. 1074-1080 
    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: Over the past two decades, membrane technology has found application in a variety of industries, ranging from water desalination to gas separations. These new applications have come about because of the availability of high-performance, permselective membranes. A key element in the development of these new membranes has been the discovery of “skinned” or asymmetric membranes. These membranes typically have an effective thickness on the order of 0.1 to 0.2 μm. They are essentially composite structures, consisting of a dense skin supported by a finely porous substrate. We now recognize that an understanding of the mechanism of formation of these asym-metric membranes is available through binary and ternary phase diagrams. Membranes for microfiltration, ultrafiltration, reverse osmosis, and gas separations are now routinely produced by some form of “phase inversion” process, amenable to explanation through phase diagram considerations.
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    Polymer Engineering and Science 25 (1985), S. 1097-1102 
    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: This paper is a sequel to an earlier one on the applicability of classical nucleation theory to second-order transitions in the Ehrenfest sense (1). In each case the approach was to obtain the critical size rc and energy barrier ΔGc for the growth of a nucleus of β-phase in an α-phase matrix by a Maclaurin series expansion of the free-energy-density g = (Gβ - Gα)/vβ as a function of θ (in BC-I) and of ΔP and Δσ in this paper where θ = (T - Tt) is the degree of undercooling and ΔP and Δσ are analogous terms for the hydrostatic pressure shift and tensile stress shift away from the equilibrium transition. The expansion coefficients were determined by the use of thermodynamic relationships. For second-order transitions, rc = 4γvβ Tt/ΔCpθ2, rc = 4γ/Δβ(Δp)2, and rc = 4γ/YαYβ(Δσ)2, respectively, for the three cases. The terms ΔCp, Δβ, and ΔY denote the differences in heat capacity, compressibility, and Young's modulus, e.g., ΔY = Yβ - Yα. The interfacial energy γαβ is denoted by γ. The activation energy barriers for the cases developed in this paper were ΔGc = (16π/3)γ3/(Δβ)2 (Δp)4 and ΔGc = (64π/3)γ3Yα2Yβ2/(ΔY)2(Δσ)4. More complicated expressions are given in the paper for the rc and ΔGc for first-order transitions. In the long run, these expressions may prove more useful than the ones for second-order because of the modifications expressions for the kinetics of transformations.
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    Polymer Engineering and Science 25 (1985), S. 1120-1121 
    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 brief introduction to the theory of block copolymer/homopolymer mixtures is presented. All important effects, such as stretching of the polymer chains, changes in the conformational entropy at an interface, enthalpic and configurational effects, as well as connectedness of the blocks of the copolymer are included in the model.
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  • 29
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    Polymer Engineering and Science 25 (1985), S. 1124-1134 
    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 morphology and mechanical properties of binary blends of nylon 6 (N6), as the major component, and ethylene-methacrylic acid copolymers (E/MAA), as the minor component, have been analyzed. It was found that the methacrylic acid content of the copolymer used as the second component has a profound effect upon the properties of the resulting blends. In particular, with increasing methacrylic acid content, the size of the domains of the E/MAA dispersed phase in the N6 matrix decreased in a regular fashion while the ultimate tensile properties increased regularly. This behavior has been attributed to a series of chemical and physico-chemical interactions taking place between the two components. The interactions are due to the presence of the acid functionality on the copolymer and do not occur when this functionality is absent. Chemical analysis of the blends was performed to confirm that chemical modification took place during the blending process.
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  • 30
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    Polymer Engineering and Science 25 (1985), S. 1164-1170 
    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 copolymer resulting from the polymerization of methyl methacrylate and styrene in the aqueous phase was tested for its mechanical and thermal properties. The usual procedure to obtain such a copolymer is by radical polymerization, but it can be done also by an ionic solution polymerization and in most cases the copolymer obtained has a statistical polymer arrangement. As this polymer is made by a complex mechanism in the presence of zinc chloride and water, it has many interesting features. The polymerization itself in the presence of water has a good industrial appeal as it simplifies considerably the operations as well as eliminates the suspension phase solvent cost. Another feature is the molecular weight distribution; we have two definite nearly monodisperse groups of polymers - one of these groups has an average molecular weight of 107. The thermal properties of the polymers were studied as functions of the polymerization conditions and a mathematical expression was derived relating these factors. The mechanical properties of this, polymer compares favorably to available industrial products.
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    Polymer Engineering and Science 25 (1985), S. 570-576 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An analysis is presented which allows the sheet or film die designer to estimate when inertial and gravitational effects are important. General theoretical equations are developed for end fed dies with arbitrary variation of the cavity cross sectional shape, cavity taper, slot length, and gap over the width. The method assumes viscous flow and a two dimensional approximation for the cavity flow. For fluid flow properties, it is assumed only that the apparent viscosity is a single valued function of the shear rate. In the important special case of constant die geometry and power law fluids, three dimensionless numbers plus the power law index are the parameters controlling the uniformity of flow from the die. Results are presented that illustrate when die orientations with respect to gravity and when fluid inertia are important. When they are not, simple expressions for die inlet pressure and uniformity index are given.
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    Polymer Engineering and Science 25 (1985), S. 589-595 
    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 flow of polymer melts in a rotating disc extruder is analyzed with the development of a mathematical model for drag flow in a contoured rotating disc. The model assumes a fully melted material which exhibits Newtonian flow behavior under isothermal conditions. Flow is evaluated in successive sections of the flow path, and the drag flow component is calculated by assuming a zero pressure gradient by analogy to the analysis of single screw extruder performance. The final expression involves a computer-assisted numerical solution. Results of the drag flow model are presented for three different disc geometries. A mathematical model of negative flow, and a comparison of the results with experimental data will be presented in followup papers.
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    Polymer Engineering and Science 25 (1985), S. 608-617 
    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: Since the cure rate of injection molded thermosets is usually very sensitive to cavity surface temperature, spatial variations in these temperatures can lengthen the necessary cure time for the entire part and cause distortion and residual stress in the molded article. This problem is addressed in the present paper by combining an optimization algorithm with a quasi-steady heat conduction analysis in the mold to determine the heating line positions and operating temperatures that minimize the spatial variation in cavity surface temperature. The method is applied to an example mold for a flat panel of uniform thickness, using two different gate locations. At a one-minute cycle, the optimal designs for each gate location dramatically reduce the variation in cavity surface temperature compared with corresponding results using a conventional heating system. These results are made more significant by the fact that the optimal designs use considerably fewer heating lines. In spite of their simplicity, the optimal designs still have enough flexibility to adjust to a changing cycle without sacrificing uniformity in cavity surface temperature.
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    Polymer Engineering and Science 25 (1985), S. 635-642 
    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 kinetics of acetylene polymerization have been studied as a function of monomer pressure, catalyst aging and concentration, Al/Ti ratio, and temperature. The rate constants of chain propagation and termination and their activation energies have been determined, The Mn of polyacetylene has been obtained using a radioquenching technique, and was found to vary from 500 to 250,000. Wide angle X-ray diffraction showed the polymer to be highly crystalline but the crystallites are disordered. The crystal structures of cis and trans polyacetylene have been obtained from the fiber electron diffraction patterns. The c-axis is the polymer chain axis which is along the fiber axis. The basic morphological entity is the microfibrils of 2 to 3 nm diameter which aggregate to form 20 to 30 nm fibrils.
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    Polymer Engineering and Science 25 (1985), S. 643-651 
    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 tensile crazing and Charpy impact behavior of polypropylene modified with styrene-butadiene copolymer (SBR) and ethylene-propylene-diene monomer (EPDM) was studied. Various rubber particle size distributions were obtained by varying the relative viscosities between rubbery phase and PP matrix. Transmission electron microscopy and computer-aided image analysis were used to provide particle size information. In general, PP blends with smaller rubber particles are tougher and more ductile than those with larger particles, probably because the former represents a more efficient use of rubbery phase in promoting crazing and/or shear yielding. Samples with average particle diameter D̄ ≥ 0.5 μm were found to exhibit pronounced crazing. Within a given sample, no crazes appeared to develop around individual rubber particles with D 〈 0.5 μm. The higher the D, the greater the propensity to form crazes. The behavior of samples with D̄ ≪ 0.5 μm appeared to be dominated by shear yielding; very few crazes could be found. That there exists a critical rubber particle size is explained by the requirement that sufficient stress concentration be maintained to a finite radial distance to permit the initiation and growth of a craze, which requires a finite volume. Small particles, inducing smaller stress-enhanced zones, are therefore not effective in initiating crazes.
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    Polymer Engineering and Science 25 (1985), S. 669-676 
    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 exit flow from a capillary is analyzed with the help of macroscopic mechanical energy and momentum balances. The analysis shows that primary normal stress differences cannot be determined from the exit pressures under the assumption that the flow is viscometric down to the exit. This assumption and the second one (made by Han [9]) that both slit and capillary exit pressures are the same would lead to unacceptable results. Published exit pressure data for polyethylene melts are shown to be unreliable because of large hole-pressure errors in the pressure measurements. Pressure profiles obtained with a thin tube technique for the flow of a poly(isobutylene) solution indicate that the flow does not remain fully developed near the exit. Moreover, it is shown that for this polymer solution the excess viscous dissipation at the exit contributes to approximately 90 percent of the exit pressure.
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    Polymer Engineering and Science 25 (1985), S. 690-697 
    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: Commercial high density polyethylene (HDPE), low density polythylene (LDPE), and linear low density polyethylene (LLDPE) resins were tested at 150, 170, and 190°C in steady state, dynamic, and extensional modes. Within the low rates of deformation \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} = ω ≤ 0.3, the steady state and dynamic functions agreed: η = η′ and N1 = 2G′; at the higher rates, the steady state parameters were larger. The elongational viscosity, ηe, was measured under a constant rate, \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \varepsilon $\end{document}, or stress, σ, condition. In the first case for LLDPE, the transient ηet reached an equilibrium plateau value, ηe. For HDPE, ηet increased up to the break point. For LDPE, stress hardening was recorded. Under constant stress the ηe, could always be determined; its value, within experimental error, agreed with the maximum value of ηet determined in a constant \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \varepsilon$ \end{document} experiment. The maximum strain at break was only ε = 1.5 for HDPE and 3, to 4 for LDPE and LLDPE. The rate of deformation dependence of the η (or η′) and ηn may be discussed in terms of the Trouton ratio, RT = ηe/3η at \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} = ω = \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \varepsilon$ \end{document}: RT ≤ 1.2 for LLDPE, RT ≤ 2.5 for HDPE, and RT ≤ 15 for LDPE. The PE resins were extruded at 190°C through a laboratory extruder equipped with a slit or rod die. The rotational speed of the screw varied from 0 to 90 rpm. Extrusion pressure, output, and energy were measured and correlated with the rheological parameters of the resins.
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    Polymer Engineering and Science 25 (1985), S. 747-750 
    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: Rheo-optical and mechanical property studies with compression molded ultra-high molecular weight polyethylene specimens at different temperatures indicate that their mechanical performance is dependent on the degree of fusion of the powder particles during compression and can be enhanced by heating the polymer powder at temperatures above 220°C. Although the mechanical performance of the compression molded specimens can be improved further by solid-state drawing at a draw ratio 5, the anisotropic morphologies from molded specimen above 220°C have higher initial slope of stress to elongation, strength to break, and an outstanding elastic recovery in compreision to the compression molded specimens at 180°C.
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    Polymer Engineering and Science 25 (1985), S. 758-764 
    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: Recent investigations on interpenetrating polymer networks (IPNs) have included two component IPNs from polyurethanes and poly(methacrylates) and two component IPNs from polyurethanes and epoxies. All the IPNs were prepared by the simultaneous polymerization technique (SIN-IPNs). Two types of IPNs, polyurethane-poly(methyl methacrylate) (PU/PMMA) and polyurethane-poly(methyl methacrylate-methacrylic acid) (PU/PMMA-MAA) were prepared. Improved phase miscibility and decreasing extent of phase separation was observed in both types of IPNs with increasing the NCO/OH ratio, decreasing molecular weight of the polyol in the PU and introduction of charge groups. A comparison was made between full-IPNs, pseudo-IPNs, graft copolymers and related homopolymers from polyurethanes and epoxies. Increased compatibility in full-IPNs and graft copolymers was observed by means of DSC, SEM and was also further substantiated by a shift toward single Tgs as determined by dynamic mechanical spectroscopy. The introduction of opposite charge groups in two-component IPNs from polyurethanes and epoxies led to improved compatibility (no phase separation) and enhanced mechanical properties.
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    Polymer Engineering and Science 25 (1985), S. 782-787 
    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 kinetic model for the rheological behavior of polymeric systems, i.e. the Berkeley kinetic network model, is compared with a generalized transient-network model. It turns out that the Berkeley kinetic network model fits quite well in the framework of the transient-network model. From the point of view of the latter model, however, a number of parameters introduced in the kinetic-network model are not independent constants as was supposed. Since the generalized transientnetwork model is totally based on microscopic assumptions, the parameters in this theory reveal information about the structure, whereas the physical interpretation of the parameters in the kinetic model is vague. Stress predictions of the generalized transient-network model agree with experimental data from a 4 percent solution of polystyrene in arochlor, obtained from literature.
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    Polymer Engineering and Science 25 (1985), S. 807-811 
    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: Experimental data on the effect of the type and amount of surface treating agents on the rheological and mechanical properties of the ferrite-filled styrene-isoprene-styrene systems at high levels of loading has been presented. The viscosities of the treated ferrite systems are found to be lower than the untreated systems, with the extent in reduction depending upon the type and amount of surface treatment. It is also found that surface treatment decreases the tensile strength and percentage elongation in the present filler-matrix system, and the extent of the decrease in viscosity as well as mechanical properties is more in the presence of titanates than with silanes.
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    Polymer Engineering and Science 25 (1985), S. 841-850 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The method proposed by C. E. Turner and J. G. Williams for characterizing the impact resistance of polymers was reanalyzed and a new method has been developed for the study of semi-ductile polymers. In these polymers, the fracture occurs by a set of stable and unstable crack propagation stages. The new model takes into account the first stable stage and the point of instability in order to allow the determination of two fracture energies Ḡst and Ginst. These fracture parameters characterize the material impact behavior. The model has been applied to polyamide 11 and 12. Molding condition and orientation effects on the impact fracture energies are presented.
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    Polymer Engineering and Science 25 (1985) 
    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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    Polymer Engineering and Science 25 (1985), S. 863-863 
    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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    Polymer Engineering and Science 25 (1985), S. 888-895 
    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: Liquid crystalline polymers can be processed to form high strength/modulus materials. In processing these materials, it is apparent that molecular orientation is an important factor in determining the physical strength of the processed materials. In this study a systematic investigation was carried out to determine how a thermotropic copolyester of parahydroxybenzoic acid (PHB) and polyethylene terephthalate (PET) responds to two basic types of flows: shear and extensional flow. This was accomplished by preparing sheared and extended samples under controlled conditions of temperature and flow history. Sheared disks were prepared using a disk and plate geometry of a Rheometrics Mechanical Spectrometer (RMS model 605), while extended ribbons were prepared using a slit die attached to an Instron capillary rheometer. Two copolymerer compositions of 60 mole percent and 80 mol percent PHB were investigated. The sheared disks and extended ribbons were investigated for molecular orientation and morphological textures using wide angle x-ray scattering (WAXS) and scanning electron microscopy (SEM) analysis, respectively. It was found that extensional flow has a greater capacity for orienting such materials than shear flow. Samples annealed at their softening points for 1 minute (240°C for the 60 mole percent PHB/PET copolymer and 300°C for the 80 mole percent PHB/PET copolymer) showed no significant loss of orientation, indicating that once orientation is produced it may remain in the melt for a long period of time. Sheared samples prepared by shearing the sample while cooling showed significantly higher degrees of orientation than those not cooled while being sheared. This may indicate that a minimum stress level exists for the production of orientation in shear flow.
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    Polymer Engineering and Science 25 (1985), S. 923-930 
    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 servo-hydraulic testing system which can simultaneously produce high loads and rapid response is described. This system allows the testing of relatively large plastic specimens, which makes it possible to perform dynamic-mechanical and transient experiments on high modulus materials, specimens routinely molded for tensile testing, and specimens removed from actual processed articles. Such large specimens also permit the use of extensometers directly attached on the gage section, providing important data for the accurate calculations of material properties. Dynamic-mechanical data on poly(methyl methacrylate), glass-filled nylon, and talc filled polypropylene specimens removed from an injection-molded dishwasher tub were obtained to demonstrate the capability of the system. Stress relaxation experiments in the nonlinear range were performed on polycarbonate to illustrate the transient testing capability of the system.
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    Polymer Engineering and Science 25 (1985), S. 947-950 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An expression is presented which can be used to correlate and predict, in an empirical fashion, polymer self-diffusion coefficients in solution over a wide range of concentrations and molecular weights, and whose parameters can be established with a minimal amount of data. Predictions thus made have been found to agree well with the limited amount of available experimental data over the entire concentration-molecular weight spectrum studied to date. This is in marked contrast to other available expressions, whose validity is confined to a narrow range of concentrations and/or molecular weights.
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  • 48
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    Polymer Engineering and Science 25 (1985) 
    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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  • 49
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    Polymer Engineering and Science 25 (1985), S. 987-1000 
    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: For batchwise radical chain solution multicomponent copolymerization, the minimum end time problem for the predetermined monomer conversion and number average molecular weight has been studied by considering the initiator concentration (or feed rate) and temperature as the two control variables. Applying the maximum principle and “unit segment treatment” (by which the co-polymerization can be treated as homo-polymerization in the kinetic analysis), it is found that for initiator addition processes the optimal initiator addition policy is to make the rate of initiation constant for the optimal temperature variation case, and the initiator concentration constant for the isothermal case as in homo-polymerization. For single charge of initiator processes, the optimal initial initiator concentration is such that it should be maintained at the lowest possible value (by which the polymerization is strongly dead-end) for the optimal temperature variation case without chain transfer steps, and at some optimal value (by which the polymerization is near dead-end) for the best isothermal case.
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  • 50
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    Polymer Engineering and Science 25 (1985), S. 32-36 
    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: Interesting phenomena were observed in the polymerization of styrene and ethylene oxide into PEO-PSt-PEO triblock copolymers using potassium naphthalene as initiator and tolusene as a solvent. The relationship between the phenomena and molecular weight of the blocks was studied. The purified and characterized triblock copolymer showed mesomorphic behavior in toluene solution which depolarized polarized light increasingly as the concentration was increased. The structure of the triblock copolymer was also studied by small-angle laser light scattering and by electron microscopy.
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    Polymer Engineering and Science 25 (1985), S. 57-63 
    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 detailed mathematical model for absolute particle-size distribution in continuous emulsion polymerization of styrene monomer is proposed on the basis of the modified population-balance theory. The computer simulation is then performed for styrene polymerization as an example of a nondesorption system. The effects of emulsifier and initiator concentrations as well as mean residence time on the absolute particle-size-distribution function, total concentration of polymer particles, conversion, average number and weight radii, average number of radicals per polymer particle, and polydispersity of radius are simulated by the model proposed.
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    Polymer Engineering and Science 25 (1985), S. 65-69 
    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: Uniaxial tension tests to, the yield point were performed on poly(hexamethylene adipamide) (nylon 6,6) as a function of temperature from 21 to 200°C at a strain rate of 2 min-1. At 21 and 60°C, measurements were also made at strain rates from 0.02 to 8 min-1. Using simple rate theory, reasonable values of activation volume were obtained, but the simple theory is inadequate to determine the activation energy. The yield-strain temperature dependence changes at 160°C as a result of a reversible crystal-crystal transition. Because of this behavior of the yield strain, the yield energy is not a linear function of temperature, as observed for several other polymers.
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    Polymer Engineering and Science 25 (1985), S. 91-97 
    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: In extruding thick polymeric objects such as bars, voids may form as a consequence of fast cooling. As is well known, this phenomenon is due to volume contraction of the inner zone which takes place when the external “shell” is already solidified. Recent experimental results on this effect show the influence of various parameters such as polymer melt viscosity, bar diameter, and operating pressure upon a critical extrusion velocity above which voids are detected. A detailed analysis of the phenomena which are thought to be relevant is presented and compared with the experimental results.
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    Polymer Engineering and Science 25 (1985), S. 105-112 
    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 frequency dependence of the complex-shear modulus of a nonbrominated flame-retardant polycarbonate has been successfully represented from 1 hertz (hz) to 1 gigahertz (ghz) at 190°C using a mechanical analog of the Cole-Cole dielectric analysis. Two sets of retardation times were required centered about 74 msec and 16 μsec. The β value for the short time response was 0.83 and for the longer time response was 0.58. The values of JoN determined from the common point at which the terminal-zone arc and the transition-zone arc touch the Jc″ = 0 axis yields an entanglement molecular weight, Me, of 1470 g/mole.
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    Polymer Engineering and Science 25 (1985) 
    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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  • 56
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    Polymer Engineering and Science 25 (1985), S. 157-163 
    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: Dynamic mechanical properties have been investigated for interpenetrating-network systems based on polyol-cured polyurethanes (PU) and 2 to 1 n-butyl acrylate-n-butyl methacrylate (Ac) networks. The systems were formed simultaneously (SIN) from all of the precursors and reactants for both networks in the same vessel, and sequentially (SIPN) by swelling a precured PU with the reactants that will form the Ac network. If the Ac network is formed after gelation of the PU, the IPNs are transparent and appear to have single T (tan δmax) between those of the homonetworks; visible-phase separation occurs if the Ac is intentionally polymerized prior to PU gelation. Damping curves were lower and broader and the T (tan δmax) and rubber moduli were higher for the SIN than for the SIPN systems. Up to 65 percent Ac, the T (tan δmax) data for both SIN and SIPN fit the Gordon-Taylor equation if a T (tan δmax) for the Ac homonetwork 7°C higher than observed is used, suggesting a higher crosslink density for the Ac network under these conditions. The differences in properties of the SIN and SIPN are assumed to be dependent on sample homogeneity and upon the presence of a tin catalyst in the SIN preparation. This can result in limited Ac-network formation and consequent phase separation before PU gelation has occurred, and the catalyst may also increase the extent of interaction, such as grafting or hydrogen-bond formation between the networks.
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    Polymer Engineering and Science 25 (1985), S. 170-177 
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    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The fatigue behavior of pure poly (vinylchloride) (PVC) and a PVC pipe compound has been investigated. Unnotched S-N lifetime, fatigue-crack growth, and craze/crack-initiation data are presented. The data trends, coupled with direct-microscopic observation, suggest that the unnotched-specimen lifetime in fatigue is dominated by the craze/crack-initiation process. This differs from the observed consistency of crack propagation and specimen-lifetime trends in several other polymers, whose failure can be traced to the initiation and growth to instability of a single dominant craze/crack.
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    Polymer Engineering and Science 25 (1985), S. 182-187 
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    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: Single Kevlar-29 fibers have been subjected to creep loading over a temperature range of 23 to 400°C for which the applied load was 50 percent that of tensile strength at each temperature considered and also subjected to a range of loads at 23°C. It has been shown that strain expressed as a logarithmic function of time describes the experimental results obtained. Up to 70 percent of breaking load, a primary creep mechanism dominates and at higher loads a secondary creep process becomes increasingly important.
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    Polymer Engineering and Science 25 (1985), S. 206-206 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A new method to obtain a rubber-modified polyamide 6 (PA6) directly during the polymerization of the caprolactam (CL) is described. Binary and ternary blends containing ethylene-propylene random copolymers (EPM) and/or a fictionalized EPM rubber (EPM-g-SA) were prepared and their morphology as well as their mechanical properties were investigated as function of composition and reaction conditions. It was found that the morphology of the blends is strongly dependent on the method of preparation. More complex structures are observed in blends obtained with the “Solution” preparation. For a better resolution of the morphology, the smooth ultramicrotomed surfaces were exposed to boiling xylene before SEM (scanning electron microscopy) examination. The rubbery phases are selectively dissolved whereas the PA6 matrix is left. The tensile mechanical properties and the Izod impact behavior are related to the mode and state of dispersion of the rubbery components. The impact properties of ternary PA6/EPM/EPMg-SA (80/18/2) and (80/15/5) blends, prepared during the CL polymerization are comparable to those of similar blends obtained by usual melt mixing procedures.
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    Polymer Engineering and Science 25 (1985), S. 250-255 
    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 deformation behavior that results from falling weight impact testing with flat-headed darts is analyzed in terms of elasticity and plasticity. From a comparison of the time and temperature dependence of the yield stress that is observed during a falling weight test with the same dependences of the yield stress during simple shear tests, it is concluded that the use of flat-headed darts results in strong shear loading. Consequently most of the plastic deformation takes place by shear flow. Of practical interest is that this leads to a simple dependence of the yield stress during the impact test and the impact energy on the plate thickness. Furthermore, for a number of cases this result allows a direct conversion of temperature effects to time effects. In practice this means that it is possible to simulate the impact behavior at very high impact rates simply by performing impact tests at lower temperatures.
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    Polymer Engineering and Science 25 (1985), S. 232-244 
    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: Free-radical polymerization of methyl methacrylate in a tubular reactor has been conducted at above-Tg temperatures. A salient feature of these experiments is the very efficient control of reactor temperature by vapor-liquid equilibrium of the polymerizing mixture via monomer evaporation. The system pressure thus provides a powerful control variable, restricting the temperature in the entire reactor by changing the monomer evaporation rate. In the range of our experimental conditions, the temperature and pressure in the reactor follow the Antoine equation closely. High temperature runs also reduce the length requirement of the reactor. However, molecular weight averages of the products are not impressive, unless slow-burning initiators are used. Modeling of above-Tg reactions has been attempted at two-levels of sophistication. A plug-flow model gives predictions in good agreement with our experimental temperatures and conversion data. The predicted molecular weights are also consistent with the experimentally observed values. However, the more elaborate rheokinctic model suggests that the superficial agreement between model and experiment is due to initiator burn-out, which limits the final conversion to within 40 percent. The liquid layer next to the reactor wall can never be so viscous as to form a stagnant deposit, due to this conversion limitation. The velocity profiles are thus not very much distorted, and a plug-flow model is adequate. With a slow-burning initiator and a sufficiently long reactor, skewing of velocity profile and reactor channeling will eventually emerge. Hence, the rheokinetic model must be evoked to model the system under such conditions.
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    Polymer Engineering and Science 25 (1985) 
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    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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    Polymer Engineering and Science 25 (1985), S. 284-288 
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    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 effect of tension during drying on the structure and mechanics of poly(p-phenylene benzobisthiazole) (PBT) fibers has been investigated. The application of tension during drying on PBT fibers spun from anisotropic solutions of PBT/Polyphosphoric acid (PPA) results in an enhancement of tensile modulus and yield strength with a reduction in strain to break. The alterations in the tensile properties can be attributed to the straightening of the wet fibrillar network and the reduction in the axial compressive stresses which develop during drying. Modifications in the mechanical behavior of PBT fibers through tension drying can be achieved regardless of the initial spin draw ratio of the fiber. Additionally, tension drying provides a means to maximize the potential stiffness of PBT fibers which have a low spin draw ratio. Lastly, these investigations show that in the processing of PBT fibers, preventing the onset of buckling and aligning the wet fibrillar network with tension during drying is more effective in enhancing the tensile properties than straightening the dried buckled fibers.
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    Polymer Engineering and Science 25 (1985), S. 48-53 
    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: Measurements have been made of the recovery of polyethylene samples from bending deformations of varying severity. The amount of spring-back from a severe bend is quite different for different densities (degrees of crystallinity), especially at short times after release, being much greater for lower-density polyethylenes. Short-term spring-back measurements thus afford a simple and rapid means of determining the approximate density. Immediate recovery is small, 5 to 15 percent, and is in rough accord with expectations for elastic-plastic solids. A major protracted recovery process follows. It is accelerated by raising the temperature, in reasonable agreement with the WLF relation for segmental mobility. It is therefore attributed to retarded molecular motions in the amorphous fraction. Final recovery is greater for lower-density materials, but it is incomplete even after very long times or for mild degrees of bending. Thus, some irreversible processes appear to take place, even when bending strains as low as 3 percent are imposed.
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    Polymer Engineering and Science 25 (1985), S. 54-56 
    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: Unsaturated polyesters were prepared by one-stage melt condensation of maleic anhydride, phthalic anhydride, propylene glycol, and poly(ethylene glycol)s with different molecular weight, and the properties of their castings from styrenated resins were investigated. Tensile and flexural properties decrease with the increase of molecular weight of poly(ethylene glycol), but impact strength, elongation, and water absorption have an inverse effect. This study improves the understanding of the effect of chain length of poly(ethylene glycol) in unsaturated polyester on the properties of its castings.
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    Polymer Engineering and Science 25 (1985), S. 698-713 
    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 mathematical model of the dynamics and heat transfer of the film embossing process has been developed. The thermal analysis around the preheat roll is determined from an unsteady, two-dimensional heat conduction equation along with appropriate boundary conditions by neglecting the curvature of the preheat roll and choosing a Lagrangian reference frame. The heat transfer occurring between the preheat roll and the embossing rolls is based on a one-dimensional analysis, including both convective and radiative effects. The deformation occurring in the nip region is analyzed for two different situations. For the case where the surface features are small in comparison with the film thickness, a modified one-dimennsional calendering analysis is given, accounting for the irregular geometry of the embossing roll surface. For the case where the polymer does not make complete contact with the surface of the engraved channel, the local deformation is determined by means of a simple one-dimensional cavity filling model. The required pressure distribution is determined by means of a simple one-dimensional cavity filling model, The required pressure distribution is determined by means of a conventional calendering analysis. The analysis for the case of a Newtonian and power-law model is presented in detail. The model yields qualitatively correct results and is computationally simple.
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    Polymer Engineering and Science 25 (1985) 
    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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    Notes: The physical properties of finished polymer blend composites are, in general, strongly influenced by the heterogeneity of the blend and the distribution of ingredients (especially reinforcement fillers) in each of the polymer phases. In this article, we review and update a processing technology specifically for the processing of multiphase rubber blend compounds in order to produce blend compounds with more desirable properties for practical applications. The basic concept is centered on the controlled-ingredient-distribution mixing (CIDM) process. The improvements in the following properties of rubber blend compounds are discussed: crack growth resistance, heat buildup, oil swelling, covulcanization, green strength, and permeability.
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    Polymer Engineering and Science 25 (1985), S. 778-781 
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    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: This paper reports the effect of humidity and temperature on the adhesive strength of a pressure sensitive adhesive (Flexbond 150) used to bond Mylar films. It has been found that, ill general, the adhesive strength decreases significantly with an increase in temperature. The effect of humidity on the bonding strength, however, was found to be process dependent. The sample preparation conditions, e.g., press weight for the bonding and the press time, are important in determining the humidity effect. The water sorption isotherm A 24°C for the adhesive was also determined. The amount of water sorbed by the adhesive at 95 percent relative pressure was found to be less than one weight percent.
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    Polymer Engineering and Science 25 (1985), S. 804-806 
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    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: Dicyanate Semi-Interpenetrating Polymer Networks (semi IPNs) are made by dissolving a thermoplastic in crosslinking dicyanates and then curing the resulting mixture. The semi IPNs produced are strong, with tensile strengths of 10,000 to 12,000 psi, and flexible, with elongations to break of 10 to 17 percent. Dicyanate semi IPNs also have good thermal stability and the softening temperatures of the IPNs are significantly, higher than those of the corresponding thermoplastics.
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    Polymer Engineering and Science 25 (1985), S. 857-862 
    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: Silane-grafted polyethylene materials are processed in conventional thermoplastic fabrication machines. The shaped articles are then crosslinked in water by the formation of Si-O-Si crosslinks. This paper represents studies on the crosslinking progress in different environments at various temperatures. Molecular orientation is shown to become permanent and mostly irrecoverable even at 150°C, in the silane-grafted solid state crosslinked specimens (the crosslinking temperature in water is well below the polymer melting temperature). These frozen molecular orientations have a significant effect on the tensile properties of the crosslinked materials causing higher yield stresses and lower elongations at break. The thermal and tensile properties of some silane-grafted crosslinked polyethylene samples and peroxide-crosslinked materials are compared and analyzed.
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    Polymer Engineering and Science 25 (1985) 
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    Keywords: Chemistry ; Chemical Engineering
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    Polymer Engineering and Science 25 (1985), S. 931-933 
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    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: Photocurable materials such as photoresists, UV-curable inks and paints, etc., can be analyzed by a variety of techniques. Commonly, these analyses are performed in a discontinuous mode, i.e., samples are exposed to light for varying times and subsequently they are subjected to analysis. Rates of reaction, conversion, etc., are determined from the residual functionalities; in the case of differential scanning calorimetry, these parameters are derived from the residual heat of reaction. In order to determine “photo speed” or sensitivity, a number of exposures of varying duration are necessary to obtain rates of reaction. By combining an exposure unit with a differential scanning calorimeter, the photoreaction can now he observed in situ. Determination of speed or rate of reaction is reduced to a single experiment. As a consequence, effects of wavelength, intensity, temperature, and environment are quickly examined as is demonstrated here for a photoresist. During the second scan residual exotherms can be used to determine reaction extend or formation of new thermally active products. Conversion may be limited if Tg rises during polymerization to exceed exposure temperatures. In addition, the formation of inaccessable functionalities has to be accounted for during evaluation.
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    Polymer Engineering and Science 25 (1985), S. 951-958 
    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: Kinetics of simultaneous interpenetrating networks (SIN) composed of a polyurethane resin (PU) and an unsaturated polyester resin was studied. A differential scanning calorimeter (DSC) was used to monitor the polymerization course. It was found that increasing the polyester content in a PU-polyester SIN enhanced the polymerization of PU due to the “solvent effect” of polyester. On the other hand, increasing the PU content in the SIN retarded the polymerization of polyester due to the “cage effect” of PU. Polymerization sequence of the SIN could be controlled by employing different initiators for polyester reaction. The degree of crosslinking in each SIN component had a significant effect on the dynamics of the SIN formation and on the limiting conversion of the polyester reartion.
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    Polymer Engineering and Science 25 (1985), S. 980-985 
    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: Orifice flow measurements have been performed at high strain rates on bulk molding compound (BMC) using convergent dies. A range of die angles and bore diameters was examined. Two models for flow behavior have been compared. It appears that, with BMC, there is a transition from constrained convergence to convergence with recirculation at a die semiangle of approximately 56 degrees.
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  • 77
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    Polymer Engineering and Science 25 (1985), S. 965-967 
    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: Interest in potential high-performance polymers, leading to characterization and development of the rodlike poly(p-phenylene benzobisoxazoles) (PBO) and poly(p-phenylene benzobisthiazoles) (PBT), has recently been extended to a related group of polymers referred to as AAPBO, ABPBO, AAPBT, and ABPBT. In this study, geometry-optimized CNDO/2 molecular orbital calculations have been carried out on AAPBO and ABPBO model compounds to determine conformational energies as a function of rotation about each type of rotatable bond within the repeat units. For AAPBO, which contains two types of rotatable bonds per repeat unit, the bond between the benzoxazole group and p-phenylene group prefers the coplanar conformation with a barrier to free rotation of 2.1 kcal mol-1, while the bond between the benzoxazole groups prefers a conformation approximately 60 degrees away from coplanarity with a barrier to coplanarity and to free rotation of 3.6 kcal mol-1. For ABPBO, which contains only the former type of rotatable bond per repeat unit, the coplanar conformations were preferred with a barrier to free rotation of 1.6 kcal mol-1. These results are in excellent agreement with the results of both theoretical and experimental studies on the structurally analogous PBO. They are also consistent with the liquid crystalline behavior found for ABPBO but not for AAPBO.
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  • 78
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    Notes: The accurate but complex McAllister model for the melt viscosities (η) of binary polymer blends has been greatly simplified by dropping the terms involving only mole fraction and molecular weight, by switching from mole fraction to mass fraction, and by making the model explicit in dynamic, rather than kinematic, viscosity. The simpler Lecyar model was tested side-by-side with the McAllister in five binary systems and at seven levels of shear rate from 5 to 500 s-1 in each system. For the 35 pairs of curves fitted, the rms standard error of estimate was 0.0945 (In η), for the Lecyar model versus 0.0911 for the McAllister; the difference corresponds to only 0.4 percent additional error in the blend viscosity. Comparison of results in two systems, reported by Carley and Crossan (12) with those of other workers, indicate that the differences among what appear to be comparable, self-consistent data sets are much greater than the within-set errors of rheometric measurement and model fitting.
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    Polymer Engineering and Science 25 (1985) 
    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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  • 80
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    Polymer Engineering and Science 25 (1985), S. 1048-1054 
    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: Blends of poly(2,6-dimethyl-1,4-phenylene oxide) (PMMPO) and poly(4-methylstyrene) (P4MS) were found to be compatible from a variety of experimental methods including calorimetric, density, and mechanical property measurements. Blend property behavior was similar to that widely reported for PMMPO/polystyrene (PS) blends. For each blend composition studied, a single glass transition temperature (Tg) was detected by differential scanning calorimetry. The compositional dependence of blend Tg was equally well represented by the empirical inverse rule of mixtures or by the Couchman thermodynamic expression. Density measurements of molded films suggested a mild excess volume of mixing that was slightly smaller than that observed for blends of PMMPO and PS. As in the case for PMMPO/PS, densification in the solid state may be associated with the observed mechanical property behavior of the PMMPO/P4MS blends. Initial modulus at each blend composition was larger than would be predicted by a simple weighted average of component polymer values. Tensile deformation changed from a ductile to a brittle mode of failure with increasing P4MS composition. The yield stress for ductile compositions and ultimate stress of brittle samples were both higher than found for the corresponding unblended polymers and higher than would be predicted from a simple additive relationship of weighted component properties. Blend impact strength determined by small strain rate tensile tests rapidly decreased to low levels with increasing P4MS composition. This drop in impact strength became more composition sensitive at higher loading rates during multiaxial deformation in an instrumented dart impact tester.
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    Polymer Engineering and Science 25 (1985), S. 1093-1096 
    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 structure formed in the coagulation stage of the spinning process of poly(p-phenylene benzobisthiazole) fiber is studied by electron microscopy. An oriented network of microfibrils with typical fibril diameters of about 80-100Å is observed. We suggest that these microfibrils are the fundamental structural elements of the fiber. Thus, knowledge of the mechanism by which this initial structure is formed may allow for better control of final fiber properties. The relation of structure formation during coagulation to the phase diagram of a rigid polymer solution and to the kinetic mechanism of the phase transition is discussed.
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  • 82
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    Polymer Engineering and Science 25 (1985), S. 1103-1109 
    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 phase transition and phase separation behavior occurring in mixtures containing an A-B block copolymer and an A homopolymer is discussed. With a pure block copolymer an order-disorder transition can be induced by raising the temperature, whereby the ordered lattice of segregated microdomains becomes unstable and gives way to a homogeneous liquid structure. Small amounts of a homopolymer added to a block copolymer can be accommodated in the microdomains consisting of the same type of monomeric units, up to a solubility limit that depends on the relative lengths of the homopolymer and the copolymer block and on the temperature. The order-disorder transition temperature of the block copolymer is also affected by the added homopolymer. At the other extreme of concentration, spherical micelles of block copolymer are formed when a small amount of the copolymer is added in the bulk homopolymer, and the critical micelle concentration again depends on the relative lengths of the molecules and blocks involved and on the temperature. Measurements were made with light scattering and small-angle X-ray scattering techniques to determine the phase behavior of mixtures containing a styrene-butadiene block copolymer and either a polystyrene or a polybutadiene. The resulting phase diagram exhibits a fascinating complexity. Comparison with recent theories treating these phenomena shows that a good agreement is generally obtained on a qualitative or semi-quantitative level, but a quantitative agreement is often not attained.
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    Polymer Engineering and Science 25 (1985), S. 1110-1117 
    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: Polymers are often formulated into detergent products in order to confer properties which facilitate processing and/or storage of the product, or to yield desirable attributes for the end-user. Carbopol resin which consists essentially of polyacrylic acid, is one such polymer. Carbopol resin systems exhibit Bingham-Body-type rheology with measurable yield-value and pronounced shear-thinning at shear stresses above the yield value. These properties render Carbopol resins useful as a thickener and a suspending agent. Interaction with other components in a formulation, however, can radically alter the thickening and suspending properties of Carbopol resins. Phase diagrams of Carbopol resins with other major components of the system can guide the formulator away from areas where undesirable interactions, such as coacervate formation, can occur, and when presented in the form of contour diagrams they quantitatively map the physical properties of interest, enabling the formulator to be guided directly into the composition region which will best satisfy his requirements. The phase diagrams can also predict when different desirable properties cannot be simultaneously achieved and they can define the extent of compromise which may be necessary in formulation of the final product.
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    Polymer Engineering and Science 25 (1985), S. 1145-1147 
    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: Poly(butylene terephthalate)PBT or Poly-1, 4-butanediyl 1, 4-diearboxylate. polycondenses readily in the presence of small amounts of organo-titanium compounds to form progressively higher molecular weight polymers, The reaction is reversible in the presence of the condensation byproduct, 1,4-butanediol. Usually this reaction is carried out in the melt phase, but the viscosity is soon limiting. In the current work the polymerization is carried out in the solid phase just below the melting point of 227°C. The equilibrium constant for this reaction is measured by subjecting the polymer to a nitrogen stream saturated with a controlled quantity of butanediol. The reaction is followed by measuring the change in the number of alcoholic end-groups by infrared spectroscopy. At about 220°C the equilibrium constant is 0.31 (σ = 0.08).
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    Polymer Engineering and Science 25 (1985), S. 1171-1178 
    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: Unprimed sapphire/nylon 6 peel joints (2.13 ± 0.27 Kg/cm) are found to be stronger than sapphire/polyethylene joints (0.06 ± 0.02 Kg/cm). Priming the sapphire with γ-aminopropyl triethoxy silane (γ-APS) improves the strength significantly resulting in adherend failure in the nylon. The rate and extent of degradation is lower with priming. The optimal silane thickness is about 1900 Å, obtained with a 0.3 percent γ-APS solution, for a five day exposure to water at 25°C. Peel joints made with 0.3 percent γ-APS film, both dried at 25°C (standard conditions) and dehydrated at 110°C under vacuum, fail cohesively when exposed at 25°C. Increasing the exposure to 55°C in a second step results in strength degradation only with dehydrated films. Lower joint strengths are obtained with five days exposure as compared to one day exposure. However, if the temperature is raised to 65°C the joints primed with standard dried films now begin to degrade and lose 90 percent of their strength in five days. Further, the nylon 6 peel joints made with a 0.3 percent γ-APS film, dehydrated for three days prior to lamination, show 10 times greater wet strengths than the corresponding PE joints. Failure surface analyses by ESCA and SEM suggest that failure locus due to water degradation is within the γ-APS layer and the failure mode is cohesive. Failure mechanics during testing the wet peel joints may also cause a partial interfacial failure mode. The effects of the silane film thickness, dehydration condition, time, and temperature dependence of the peel strength degradation indicates that the structure of the γ-APS layer plays an important role in the promotion and retention of adhesion with a thermoplastic polymer system capable of limited primary interactions through possible interdiffusion with the silane layer.
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    Polymer Engineering and Science 25 (1985), S. 1035-1040 
    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: This paper presents the results of a testing program carried out on the fracture properties of poly(methyl methacrylate) (PMMA). The objective of the program was to determine the validity of using standard impact test methods to obtain fracture data, as opposed to the more expensive fracture toughness tests. It was found that impact test results may be used to evaluate fracture properties for PMMA with correlation being obtained with fracture toughness test data.
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    Polymer Engineering and Science 25 (1985), S. 1056-1068 
    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: Blends of poly(vinyl chloride) with chlorinated poly(vinyl chloride) (PVC), and blends of different chlorinated poly(vinyl chlorides) (CPVC) provide an opportunity to examine systematically the effect that small changes in chemical structure have on polymer-polymer miscibility. Phase diagrams of PVC/CPVC blends have been determined for CPVC's containing 62 to 38 percent chlorine. The characteristics of binary blends of CPVC's of different chlorine contents have also been examined using differential calorimetry (DSC) and transmission electron microscopy. Their mutual solubility has been found to be very sensitive to their differences in mole percent CCl2 groups and degree of chlorination. In metastable binary blends of CPVC's possessing single glass transition temperatures (Tg) the rate of phase separation, as followed by DSC, was found to be relatively slow at temperatures 45 to 65° above the Tg of the blend.
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  • 88
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    Polymer Engineering and Science 25 (1985), S. 1081-1087 
    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 products of random copolymerizations are heterogeneous in chemical composition, having a distribution of the fraction of each monomer in the copolymer. Polymer molecules with the same composition and molecular weight can be treated as separate components in a polymer blend. The spinodal limit is a simple function of chemical heterogeneity. The equilibrium number of phases, phase volumes, and average composition can be calculated from the condition that the chemical potential of a polymer species is equal in every phase. Phase diagrams are calculated for various hypothetical chemical distributions as well as a distribution characteristic of a random acrylonitrilebutadiene copolymerization to high conversion.
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    Polymer Engineering and Science 25 (1985), S. 1118-1119 
    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 brief overview of the effects of chain length distribution, branching, chemical distribution, and deuterium labeling on phase equilibria is presented.
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    Polymer Engineering and Science 25 (1985), S. 1123-1123 
    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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    Polymer Engineering and Science 25 (1985), S. 1135-1138 
    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 effects of temperature on the specific volumes and thermal expansivities for a range of amorphous polymers, above and below the glass transition temperature, are treated on the basis of the physical properties of polymers. The results are found to be in good agreement with observed data. The analysis of the results shows that the temperature derivative of the zeropressure thermal expansivity of the liquid polymer increases with increasing temperature. The change in the thermal expansivity, Δα = αOL - αOG, decreases with increasing temperature.
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    Polymer Engineering and Science 25 (1985), S. 724-726 
    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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    Polymer Engineering and Science 25 (1985), S. 751-757 
    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 contributions of the cis and trans configurations of the main chain double bonds to the transition temperatures and rheological properties were determined for four well-defined polymaleamides, which were prepared by the room temperature ring-opening, step-growth polymerization reactions of N,N′-bisisomaleimide monomers with bifunctional primary diamines. The polymaleamides were glassy solids, which could be thermally isomerized into related polyfumaramides. The glass transition temperatures of the polyfumaramides, as determined by mechanical spectrometry, are systematically and markedly higher than those of the polymaleamides from which they were derived.
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    Polymer Engineering and Science 25 (1985) 
    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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  • 95
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    Polymer Engineering and Science 25 (1985), S. 797-803 
    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 flow behavior of random copolymers of styrene and butyl methacrylate containing specific carbon blacks varying in surface area were studied at various temperatures and shear rates. Master curves of reduced viscosity as a function of shear rate were prepared for the pure copolymers at 150°C. The superposition required vertical and horizontal shifts, proportional to (aT)-1 and (aT).53, respectively, where aT is the shift factor. With the incorporation of carbon black, the viscous response is non-Newtonian exhibiting a yield stress at increasing filler concentration and surface area. Master curves of viscosity against shear rate were generated at fixed filler loadings and surface areas by using a single horizontal shift factor.
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    Polymer Engineering and Science 25 (1985), S. 828-833 
    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 mechanism underlying fracture of many oriented semicrystalline polymers is hypothesized to be a thermally activated, stress-aided rate process in which the tie chains connecting crystalline units suffer thermomechanical dissociation. Some previous numerical models based on this concept have assumed a Gaussian distribution of tie chain contour lengths which are ruptured progressively by successively higher specimen strains, and have used electron spin resonance (ESR) spectroscopy to obtain the numerical parameters of the distribution. The distribution of tie chain lengths in the intererystalline region is calculated theoretically in this paper, based on minimization of free energy. Our results, although in basic agreement with earlier models, suggest a reinterpretation of some of the ESR findings with regard to molecular fracture processes.
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    Polymer Engineering and Science 25 (1985), S. 851-856 
    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: Properties of a branched polyester ether elastomer have been examined by using two widely differing preparation methods: (1) prepared to final molecular weight by using melt polycondensation (MP) and (2) prepared to an intermediate molecular weight by using melt polycondensation followed by solid phase polycondensation to the final molecular weight (SP). Differences in Tm were attributed to annealing during the SP process and also to apparent changes in monomer sequence distribution in the polymer chains. Crystallization during cooling (DSC) and melt viscosity appeared to be solely a function of molecular weight rather than of preparation history. Molecular weight distribution was exponentially dependent on viscosity average molecular weight for the MP samples, but the distribution was linearly dependent for the SP case which more nearly represents equilibrium conditions. Polymer mechanical properties did not vary much in spite of the pronounced differences observed.
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    Polymer Engineering and Science 25 (1985), S. 875-887 
    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: Since only minor structural rearrangements occur prior to yielding, the axial and off-axis yield stress of a polymer sample is expected to relate to the initial structural state of the material. Samples of uniaxially oriented isotactic polypropylene films with known structural state parameters have been deformed under a uniaxial tensile stress at deformation rates of 20 percent and 100 percent per minute over an angular range from 0 to 90 degrees to the fabrication direction. The axial yield stress data was found to correlate with the initial noncrystalline orientation state of the undeformed sample. The axial and offaxis yield stress data was fit to the Hill equation derived for the application of a uniaxial tensile stress. The experimentally determined coefficients from the best fit of the yield stress data to the Hill equation were related to the measured structural state parameters. These correlations allow prediction of the yield stress of an anisotropic film at any angle to the film symmetry axis from knowledge of the measured structural state parameters alone.
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    Polymer Engineering and Science 25 (1985), S. 909-920 
    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: Based on the concept of entropy of mixing, a new method for determining the degree of mixing of the filler in a polymer matrix has been established. The measurement used in this method is based on a new variable, the effective volume fraction of the filler, φ′, which is a function of the mixing index, A, and the volume fraction of the filler, φ. The mixing index can be determined from the tensile modulus data of filled elastomers. Excellent agreement is obtained between the mixing index and the dispersion of the filler as determined by a morphological study of cryogenically fractured surfaces of filled elastomers. Using the new variable, the effective volume fraction of the filler, useful relationships for the tensile modulus and the ultimate stretch ratio of filled elastomer have been established. Experimental data confirm that these relationships can well describe the effects of concentration and degree of mixing on the two tensile properties of filled elastomers.
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    Polymer Engineering and Science 25 (1985), S. 934-941 
    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 equilibrium phase behavior of the partially miscible system polystyrene-polybutadiene-chloroform was studied at 25°C and 1 atm pressure by using gel permeation chromatography to analyze the conjugate phases. Three narrow molecular weight distribution samples of each polymer were used to provide nine examples of the system for study. The Flory-Huggins theory was used to determine the polymer-polymer interaction parameter χ23, When literature values of the two polymer-solvent interaction parameters χ12 and χ13 were used, the χ23 values generally were found to be negative and to show no distinct concentration dependence. No significant improvement was found when the literature value of only the polybutadiene-chloroform interaction parameter was used to simultaneously generate values of χ23 and χ12. Values of χ23 at the critical point, χ23,cr, were found to increase with increasing polymer concentration.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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