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  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1061-1080 
    ISSN: 0887-6266
    Schlagwort(e): polymer blends ; dilatometry ; free volume ; specific volume ; excess volume ; compressibility ; thermal expansivity ; equation of state ; scaling parameters ; crystallinity ; glass transition ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Melt-miscible polymer blends of poly(ethylene oxide)/atactic poly(methyl methacrylate (PEO/a-PMMA)) were prepared by melt-mixing and characterized by pressure-volume-temperature (PVT) dilatometry in the pressure and temperature range of 0 to 200 MPa and 20 to 200°C, respectively. The PVT data were analyzed in terms of two equations of state (EOS). The empirical Tait EOS was applied in the glassy, semicrystalline, and equilibrium melt state, and the Simha-Somcynsky EOS theory was applied in the equilibrium melt and glassy state. The Simha-Somcynsky EOS theory contains a free volume function. The temperature, pressure, and composition dependence of the free volume fraction h calculated from the Simha-Somcynsky EOS theory was studied. As a function of blend composition we observe that the free volume fraction, thermal expansivity, and compressibility all deviate mainly positively from linearity while the specific volume deviates mainly negatively from linearity. These findings are reconciled with composition-dependent free volume parameters, the free volume and cell volume as well as with self- and cross-interaction parameters derived from the Simha-Somcynsky EOS theory as applied to polymer mixtures. Moreover, the pressure dependence of glass and melting transitions as well as crystallization kinetics have been investigated. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1061-1080, 1998
    Zusätzliches Material: 18 Ill.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 755-761 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation lifetime spectroscopy ; free volume ; transition temperatures ; poly(silylenemethylene)s ; dynamic mechanical analysis ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Amorphous and crystalline poly(silylenemethylene)s with the repeating PhRSiCH2 (R : Me or Ph) units were characterized by positron annihilation lifetime spectroscopy (PALS) to gain insights into the molecular motions of these polymers. The temperature dependence of the ortho-positronium lifetime (τ3) and intensity (I3) was examined from 50 to 470 K for each sample. The glass transition temperature of each polymer was easily distinguished by a change in the slope of τ3 spectrum. Both polymers exhibited a steep drop of I3 at 130-140 K being probably assignable to the transition arising from the motions of phenyl groups, which was almost undetectable by means of differential scanning calorimetry or dynamic mechanical analysis. Several other transitions of these polymers detected by PALS are also discussed. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 755-761, 1998
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 797-803 
    ISSN: 0887-6266
    Schlagwort(e): polynorbornene ; gas separation ; membrane ; free volume ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A study of gas transport properties of novel polynorbornenes with increasing length of an aliphatic pendant group R (CH3—, CH3(CH2)3—, CH3(CH2)5—, CH3(CH2)9—) has been performed. These polymers were synthesized using novel organometallic complex catalysts via an addition polymerization route. This reaction route maintained the bridged norbornene ring structure in the final polymer backbone. Gas permeability and glass transition temperature were found to be higher than those for polynorbornenes prepared by ring-opening metathesis and reported in the literature. It was shown that for noncondensable gases such as H2 and He the selectivity over N2 decreased when the length of the pendant group increased, but remained relatively stable for the more condensable gases (O2 and CO2). The permeability coefficient is correlated well to the inverse of the fractional free volume of the polymers. The more condensable gases showed a deviation from this correlation for the longest pendant group, probably due to an increase of the solubility effect. This polymer series demonstrated a simultaneous increase in permeability and selectivity, uncommon for polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 797-803, 1998
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 861-871 
    ISSN: 0887-6266
    Schlagwort(e): glass transition ; polymer blends ; free volume ; positron annihilation ; composition dependence of Tg ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: High-Vinyl Polybutadiene (HVBD)/cis-Polyisoprene (CPI) blends were characterized by Differential Scanning Calorimetry (DSC) and Positron Annihilation Lifetime Spectroscopy (PALS). A single DSC glass transition temperature Tg is observed, whose composition dependence strongly deviates from additivity, and shows an apparent cusp when the weight fraction of HVBD ≈ 0.75. The free-volume hole size, Vh, and the scaled fractional free volume, hps/C, = I3Vh were determined by PALS from the orthopositronium (o-Ps) intensities, I3, and lifetimes, τ3, over a temperature range encompassing Tg and the temperature at which “positronium bubble” formation occurs. In the glass, Vh and hps/C are smaller for CPI than for HVBD, but the thermal expansion coefficient for hole volume, αf, is larger in the melt for CPI than for HVBD; thus, an iso-hole volume temperature occurs in these blends at Tiso ≈ -34°C. Above and below Tiso, Vh and hps/C each show a negative departure from additivity. A quantitative interpretation of the cusp in the composition dependence of Tg can be obtained, via a modified analysis of Kovacs, using free-volume quantities from PALS, with the ratio of scaling constants CCPI/CHVBD as an adjustable parameter. At high temperatures, the positron bubble size is smaller in CPI than in HVBD. This agrees with the observation that the thermal expansivity of hole volume, and, hence the internal pressure are larger in the equilibrium melt of CPI. The effect of e+-irradiation on the o-Ps intensity was investigated. I3 decreases more rapidly in the melt as T → Tg, and then more slowly in the glass, suggesting that the effect is due to trapping of radical or ionic species which inhibit o-Ps formation. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 861-871, 1998
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 463-471 
    ISSN: 0887-6266
    Schlagwort(e): hydrogel ; free volume ; positron annihilation ; water ; density ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A copolymer of 2-hydroxyethyl methacrylate (HEMA) with 2-ethoxy ethyl methacrylate (EEMA) was synthesized and the molecular mobility, free volume, and density properties examined as a function of composition. These properties were correlated with the equilibrium water uptake in order to determine which of the properties were most influential in causing high water sorption, as these materials are suitable candidates for hydrogel systems. It was found that the polar HEMA repeat unit results in a rigid, glassy sample at room temperature due to the high degree of hydrogen bonding between chains whereas high EEMA content leads to rubbery samples with subambient glass transition temperatures. The free volume properties on the molecular scale measured by positron annihilation lifetime spectroscopy (PALS) showed that higher HEMA content led to smaller, fewer holes and a lower free volume fraction than EEMA. Therefore the high water uptake of HEEMA-containing copolymers is largely related to the high polarity of the HEMA unit compared to EEMA, despite the low content of free volume into which the water can initially diffuse. Trends in density with copolymer composition, as measured on a macroscopic level, differs to that seen by PALS and indicates that the two techniques are measuring different scales of packing. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 463-471, 1998
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1465-1481 
    ISSN: 0887-6266
    Schlagwort(e): poly(phenylene) ; dielectric ; dynamic mechanical ; relaxation ; free volume ; positron annihilation ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The free volume and related mobility properties of substituted poly(p-phenylene) polymers are examined. The techniques used range from positron annihilation, dielectric relaxation, and dynamic mechanical spectroscopy to thermally stimulated currents. Fractional free volume is determined for the samples with different substituted side groups and related to the glass transition temperature. Bulkier groups lead to a greater fractional free volume and lower glass transition temperatures. Comparison of molecular relaxation times using the different characterization techniques demonstrates that there is strong coupling between motion of the main chain and the side groups, on which the dipoles reside. Intermolecular coupling between the main chains at the primary relaxation is shown in this work to be related to the nature of the side chains and resultant free volume, as are the temperature locations of local, secondary relaxations. A qualitative model describing the effect of regiochemistry on the motions and packing of these materials is also proposed. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1465-1481, 1998
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1839-1845 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; polymers ; free volume ; plasticization of polymers ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Positron lifetime measurements in pure polyvinyl chloride (PVC) and in the plasticized PVC have been performed. Tricresyl phosphate was used as a plasticizer. Samples of the PVC were prepared with eight different plasticizer concentrations (from 0 to 35% of the plasticizer in the PVC). All of the measurements were performed in air at room temperature. A conventional fast-slow coincidence lifetime spectrometer was used for the measurements. Mean free volumes radii and fractional free volumes were calculated from the lifetime data. It has been found that the mean free volume radius is in the investigated region of the plasticizer concentrations, a linear function of the concentration of the tricresyl phosphate in the PVC. It seems that a polynomial fit can be used to describe the fractional free volume vs. the plasticizer concentration in the PVC. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1839-1845, 1998
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1513-1528 
    ISSN: 0887-6266
    Schlagwort(e): free volume ; thermal expansion ; positron lifetime measurements ; semicrystalline polymers ; polyethylene ; polytetrafluoroethylene ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Positron lifetime measurements, performed in the temperature range 80-300 K, are reported for polyethylene (PE) and polytetrafluoroethylene (PTFE). The lifetime spectra have been analyzed using the data processing routines LIFSPECFIT and MELT. Two long-lived components appear, which are attributed to pick-off annihilation of ortho-positronium in crystalline regions and at holes in the amorphous phase. The ortho-positronium lifetimes, τ3 and τ4, are used to estimate the crystalline packing density and the size of local free volumes in the crystalline and amorphous phases. The interstitial free volume in the crystals exhibits a weak linear increase with the temperature which is attributed to thermal expansion of the crystal unit cell. In the amorphous phase, the hole volume varies between 0.053 and 0.188 nm3 (PE) and between 0.152 and 0.372 nm3 (PTFE). Its temperature variation may be fitted by two straight lines, the intersection of which is used to estimate a glass transition temperature of Tg = 195 K for both PE and PTFE. The slopes of the free volume in the glassy and crystalline phases with the temperature correlate well with each other. The coefficients of thermal expansion of the hole volume are compared with the macroscopic volume change below and above the glass transition. From this comparison a fractional hole volume at Tg of 4.5 (PE) and 5.7% (PTFE) and a number of 0.73 (PE) and 0.36 (PTFE) × 1027 holes/m3 is estimated. Finally, it is found that the intensity of o-Ps annihilation in crystals shows a different temperature dependence to that in the amorphous phase. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1513-1528, 1998
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1739-1746 
    ISSN: 0887-6266
    Schlagwort(e): block copolymers ; molecular diffusion ; Forced Rayleigh scattering ; free volume ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Forced Rayleigh scattering was used to investigate the diffusion of a photoreactive dye molecule in two homogeneous poly(styrene-b-isoprene) (SI) diblock copolymers with overall molecular weights of approximately 2000. Although diffusion rates were intermediate to TTI transport in homopolymer polystyrene (PS) and polyisoprene (PI), system dynamics appear to be largely dictated in each case by the PI block. The size of the polymer jumping unit, on the other hand, is evaluated from a free-volume analysis of the data, and is found to be governed predominantly by the PS component of the copolymer. The mechanism for tracer diffusion in low-molecular-weight block copolymers appears analogous to transport in a high molecular weight SI diblock copolymer (Mn = 13,600) that has been solvated sufficiently in toluene to be microstructurally disordered. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1739-1746, 1998
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2111-2128 
    ISSN: 0887-6266
    Schlagwort(e): orientation ; physical aging ; free volume ; glass-transition ; dilatometry atactic-polystyrene ; bisphenol A polycarbonate ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: It has recently been demonstrated that hot-drawn samples of bisphenol A polycarbonate (PC) have a 50% higher volume relaxation rate than their isotropic counterpart even though the oriented samples have a lower initial free volume (i.e., higher density).1 In an attempt to better understand this paradox, samples of unaged, hot-drawn PC were characterized thermodynamically and kinetically as a function of orientation. Heat capacity, hole energy, and Tg data indicate that the chain mobility is actually decreasing slightly with orientation, possibly due to the hindered motion brought about by tighter packing, stronger intermolecular bonding, and reduced free volume. Nonetheless, this decrease in localized mobility is in contradiction to the enhanced volume relaxation rates observed for the oriented samples. In contrast, dynamic mechanical data indicate an increase in the relaxation strength of the β-transition (-100°C at 1 Hz) upon stretching for both the stretch and transverse directions. This implies that more segments are actively participating in the relaxation process for the oriented samples even though their individual localized mobility might be slightly lower. The net result is an increase in “effective” mobility for the oriented samples. It is conjectured that the enhanced relaxation strength of the oriented samples is a result of the stretching process somehow activating more of the chains into a higher energy state, and may be related to the physical aging concept of stress-induced rejuvenation/acceleration. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2111-2128, 1998
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
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  • 11
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 3035-3048 
    ISSN: 0887-6266
    Schlagwort(e): epoxy ; absorption ; water ; positron annihilation lifetime spectroscopy ; free volume ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Epoxy resins absorb significant quantities of moisture, typically 1 to 7% by weight for various formulations, which can greatly compromise their physical properties. It is known that polarity of the epoxy is a significant factor in determining the ultimate moisture uptake. However, the contribution from molecular topology still remains vague. In this work, the effects of molecular topology are elucidated by synthesizing novel epoxies where the polarity is maintained constant but the topology is systematically altered. The molecular topology is quantified in part via Positron Annihilation Lifetime Spectroscopy (PALS) in terms of the nanometer-sized voids, or nanovoids, that are also commensurate with typical interchain distances. The nanovoids are separated into their absolute zero and thermally fluctuating fractions by performing PALS measurements over a wide range of temperatures. A strong correlation is observed between the absolute zero hole volume fraction and the ultimate moisture uptake. Although the correlation is clear, the absolute zero hole volume fraction alone is not sufficient to predict the ultimate moisture uptake, and network polarity must also be considered. It is surmised that the role of the nanovoids is to open the epoxy matrix and alleviate steric hindrances that may prevent a water molecule from associating with a polar group. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 3035-3048, 1998
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 12
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 3049-3056 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; free volume ; polysulfone ; CO2 gas exposure ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Positron annihilation lifetime (PAL) spectroscopy has been employed to study subnanometer hole properties in polysulfone (PSF). In this study, hole properties of size, fraction, and distribution of PSF exposed to CO2 are reported. In the PSF/CO2 system, the hole size and fraction significantly increase and the free-volume distribution broadens as a function of CO2 pressure in the range of 0-1000 psi. Hysteresis in hole properties is observed during CO2 sorption/desorption cycle. The high sensitivity of PAL results due to CO2 exposure in PSF is explained in terms of the microstructural changes in the polymer matrix, i.e., filling penetrant and plasticization, gas hydrostatic pressure effect, and creation of free volumes and holes. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 3049-3056, 1998
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 13
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1141-1151 
    ISSN: 0887-6266
    Schlagwort(e): polymer gel ; poly(N-isopropylacrylamide) ; PNIPA ; volume phase transition ; hydrogen bond ; hydrophobic interaction ; free volume ; positronium ; positron annihilation ; methanol-water mixed solvent ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The macroscopic volume shrinkage and swelling of poly(N-isopropylacryl-amide) (PNIPA) gel induced by the compositional change in the methanol-water mixed solvent is correlated to the change in the nanoscopic free volume size and numerical concentration formed in the PNIPA gels. The free volume size and numerical concentration are estimated from the longest component appearing in the positron annihilation lifetime curves. The apparent free volume fraction calculated by the free volume size and numerical concentration, and dispersion of the free volume deduced by the size distribution are utilized to analyze the origin and location of the free volumes. The free volume parameters obtained by analysis of the positron annihilation data show various nanoscopic phases occuring within the PNIPA gels during the volume change, implying the variation of the strength of the interactions among the solvent molecules and the polymer chains of the PNIPA. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1141-1151, 1998
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1737-1746 
    ISSN: 0887-6266
    Schlagwort(e): free volume ; dual mode ; diffusion ; glassy polymer ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The development of a new model for the diffusion of gas molecules in glassy polymers is presented which utilizes concepts from free volume theory and relies on a dual-mode interpretation of sorptive dilation in glassy polymers. Three assumptions are made in the development of the model. First, the free volume available for molecular transport processes is taken as constant below the glass transition temperature. Second, two populations of gas molecules are assumed to exist - one which contributes to the maintenance of an iso-free volume state upon sorptive dilation and one which does not contribute owing to sorption into regions of unrelaxed volume. Third, the former population is assumed to be mobile while the latter is not. The resulting model predicts, at constant temperature, a diffusion coefficient that is independent of solute volume fraction. This is in contrast to the widely used dual-mode sorption model with partial immobilization for gas transport in glassy polymers which leads to a diffusion coefficient that is dependent on solute mole fraction through the molar gas concentration. The new model is used to interpret gas transport data from permeation experiments for carbon dioxide, methane, and ethylene in three polycarbonates. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1737-1746, 1997
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 15
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1855-1868 
    ISSN: 0887-6266
    Schlagwort(e): gas permeability ; permselectivity ; activation energies ; free volume ; polyimides ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Gas transport of helium, hydrogen, carbon dioxide, oxygen, argon, nitrogen, and methane in three soluble poly(phenylene sulfone imide)s based on 2,2-bis(3,4-decarboxyphenyl) hexafluoropropane dianhydride (6FDA) has been investigated. The effects of increasing length of well-defined oligo(phenylene sulfone) units on the gas permeabilities and diffusivities were determined and correlated with chain packing of the polymers. Activation energies of diffusion and permeation were calculated from temperature-dependent time-lag measurements. The influences of the central group in the diamine moiety of 6FDA-based polyimides on physical and gas transport properties are discussed. The incorporation of a long oligo(phenylene sulfone) segment in the polymer backbone decreases gas permeability and permselectivity simultaneously. The decreases in permeability coefficients can be mainly related to decreases in diffusion coefficients. Changing the central group of diamine moiety from —S— to —SO2— leads to a 45-50% decrease in CO2 and O2 permeabilities without appreciable increase in the selectivities. This is considered to be due to the formation of charge transfer complexes. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1855-1868, 1997
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 16
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 771-776 
    ISSN: 0887-6266
    Schlagwort(e): Nafion ; positron annihilation ; free volume ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: We report a new result on positron annihilation studies in acid- and cation-neutralized (Li+, Na+, K+, Rb+, Cs+, UO22+, Ni2+) Nafion membranes using positron lifetime and Doppler-broadened annihilation radiation (DBAR) measurements. The free-volume structure is characterized using a simple quantum mechanical model of positronium (Ps) in a spherical well. Our studies indicate that formation and expansion of clusters is always associated with a change in free-volume structure resulting in smaller free-volume holes. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 771-776, 1997
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 17
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 523-534 
    ISSN: 0887-6266
    Schlagwort(e): polymer solutions ; supercritical fluids ; non-Newtonian viscosity ; free volume ; polydimethylsiloxane ; carbon dioxide ; capillary rheometer ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Viscosity curves were measured for polydimethyl siloxane (PDMS) melts swollen with dissolved carbon dioxide at 50 and 80°C for shear rates ranging from 40 to 2300 s-1, and for carbon dioxide contents ranging from 0 to 21 wt %. The measurements were performed with a capillary extrusion rheometer modified for sealed, high-pressure operation to prevent degassing of the melt during extrusion. The concentration-dependent viscosity curves for these systems are self-similar in shape, exhibiting low-shear rate Newtonian plateau regions followed by shear-thinning “power-law” regions. Considerable reduction of viscosity is observed as the carbon dioxide content is increased. Classical viscoelastic scaling methods, employing a composition-dependent shift factor to scale both viscosity and shear rate, were used to reduce the viscosity data to a master curve at each temperature. The dependence of the shift factors on polymer chain density and free volume were investigated by comparing the shift factors for PDMS-CO2 systems to those obtained by iso-free volume dilutions of high molecular weight PDMS. This comparison suggests that the free volume added to PDMS upon swelling with dissolved carbon dioxide is the predominant mechanism for viscosity reduction in those systems. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 523-534, 1997
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1107-1116 
    ISSN: 0887-6266
    Schlagwort(e): enthalpy relaxation ; conformational energy ; free volume ; glass transition ; side chains ; physical ageing ; Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The enthalpy changes ΔH∞ between a poly(vinyl acetate) glass formed by rapid cooling and the corresponding fully relaxed glass have been estimated at four temperatures below the glass transition. The values obtained were different to those expected by extrapolating liquid behavior below the glass transition and were found to agree well with the predictions of a simple expression for the combined main chain conformational and free volume contributions to enthalpy. Conformational contributions from the side chain alone were also considered but were not required to obtain agreement with experiment. It can be concluded that the side chains remained mobile below the glass transition and do not contribute to the heat capacity discontinuity at Tg. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1107-1116, 1997
    Zusätzliches Material: 6 Ill.
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  • 19
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2145-2151 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; free volume ; relaxation ; local motion of molecule ; micro-Brownian motion ; polyethylene ; polystyrene ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Relaxation processes in polyethylene (PE) and polystyrene (PS) were studied by positron annihilation technique. For PE, above the glass transition temperature, Tg, the size of free volumes and its concentration were increased by the micro-Brownian motion of molecules. For PS, local motions of molecules in backbone chains were found to start above 260 K. However, these local motions were suppressed by an interphenyl correlation. For both PE and PS, below 250-260 K, the formation probability of positronium atoms increased with decreasing temperature. This fact was assigned to the freezing in of the local motions of molecules. For PS, an onset of the local motions of molecules was observed above 100 K. These motions were expected to be associated with liberation of phenyl groups. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 20
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 121-130 
    ISSN: 0887-6266
    Schlagwort(e): self-diffusion ; mutual diffusion ; activation energy ; free volume ; segmental motion ; inverse gas chromatography ; static gradient NMR ; 1,3,5-triisopropylbenzene ; polystyrene ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Self-diffusion coefficients of 1,3,5-triisopropylbenzene (TIB) in binary solutions with polystyrene and ternary mixtures comprised of TIB, toluene, and polystyrene have been measured by static gradient nuclear magnetic resonance (SG-NMR) techniques. These data, as well as mutual-diffusion coefficient data measured by capillary column inverse gas chromatography (CCIGC), have been analyzed here with the Vrentas-Duda free-volume diffusion model. Although both binary and ternary diffusion coefficient data can be accurately correlated with the model, the results contradict those of an earlier investigation, which suggested that TIB diffuses as a single unit in polystyrene solutions. The new data suggest that either: 1) TIB diffuses by piece-wise displacements in polystyrene solutions, or 2) a diffusive activation energy ceiling value has been reached. The implications of both possibilities are discussed in the context of established free-volume principles. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 21
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1189-1195 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; glass transition ; free volume ; polystyrene ; lifetime ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Free volume characteristics in three samples of monodisperse polystyrene were investigated by positron annihilation technique over a temperature range from 300 to 380 K. The number-average molecular weight of the samples ranged from 5730 to 1,524,000. The observed lifetime spectra were resolved into three components, where the longest lifetime, τ3 was associated with the pick-off annihilation of ortho-positronium (o-Ps) trapped by free volumes. The change of the temperature coefficient of τ3 was observed at around 350 K, at which the value of τ3 was a constant value of 2,3 ns for all specimens with different molecular weights. There was no discrete change of τ3 in intensity, which is corresponding to the number of free volumes. The size of free volume at glass transition was evaluated to be 0.l nm3. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 22
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2767-2770 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; positron lifetime ; free volume ; PTFE ; silica ; composites ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Positron annihilation lifetime spectroscopy (PALS) was used to study the microstructure of PTFE/silica composites. The positron lifetimes (τn) and intensities (In) of PTFE and the composites (30-62% silica) were measured at room temperature as a function of specimen thickness. Four lifetime components were found in PTFE and the composites. The longer lifetime components, τ3 = 1.4 ns and τ4 = 4.4 - 4.1 ns, were interpreted to be due to the presence of two different sized free volume cavity distributions within the PTFE/silica composites. A strong silica concentration dependence was found in the bulk intensities (I3b and I4b). The I3b value increased from 13.0% in PTFE to 28.2% in the 62% composite, while the I4b value decreased from 17.5% in PTFE to 4.5% in the 62% composite. The smaller-void size, free volume fraction (τ3I3b) values increased linearly between 0 and 100% silica concentration, while the larger void size, free volume fraction (τ4I4b) values decreased nonlinearly with silica concentration. Since silica has a long lifetime component (τ3 = 1.6 ns), this behavior is ascribed to silica particles occupying the large free volume cavities (370 Å3) in the PTFE/silica composites. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 23
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2979-2985 
    ISSN: 0887-6266
    Schlagwort(e): anisotropy ; free volume ; oriented polymers ; positron annihilation ; correlation ; 2D-ACAR ; polycarbonate ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Two-dimensional angular correlation of annihilation radiation (2D-ACAR) experiments have been performed on an uniaxially oriented polymer, bisphenol-A polycarbonate. The two-dimensional hole structures of unoriented and oriented polymers, determined from the momentum distributions, are found to be spherical and ellipsoidal, respectively. The average hole radii are determined to be 2.9 Å in the unoriented sample and between 2.3 and 3.8 Å in the oriented sample. Applications of the 2D-ACAR method to image the three-dimensional hole structures of polymeric materials are discussed. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 24
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1659-1664 
    ISSN: 0887-6266
    Schlagwort(e): positron annihilation ; free volume ; liquid-crystalline polymer ; nematic ; smectic ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Free volumes in thermotropic side-chain liquid-crystalline polymers were probed by positron annihilation technique. Lifetime spectra of positrons were measured in the temperature range between 130 and -60°C in cooling. For a nematic liquid-crystalline polymer (polyacrylate), the lifetime of ortho-positronium (τ3) was decreased with decreasing temperature above the glass transition temperature (Tg, 21°C) with larger temperature coefficient than that below Tg. The intensity of ortho-positronium (I3) was constant above Tg. These facts mean that the size of the free-volume holes decreased with the decreasing the temperature but the concentration was almost constant in nematic phase. For a smectic liquid-crystalline polymer (poly(p-methylstyrene) derivative), a discontinuous decrease in the value of τ3 and that of I3 were observed at 107°C, which was the transition temperature from smectic to crystalline phase. Such discontinuous changes were not observed for the polyacrylate specimen. This difference was considered to be attributed to the higher-ordered structure of the smectic phase. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 25
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1903-1906 
    ISSN: 0887-6266
    Schlagwort(e): Positron annihilation ; polymers ; free volume ; plasticization of polymers ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Positron lifetimes measurements in pure polyvinyl chloride (PVC) and in the plasticized PVC have been performed. Dioctyl phthalate has been used as a plasticizer. Samples have been prepared of the PVC with eight different plasticizer concentrations (from 0 to 35% of the plasticizer in the PVC). All of the measurements have been performed in air at room temperature. A conventional fast-slow coincidence lifetime spectrometer has been used for the measurements. Mean free volumes radii have been calculated from the lifetime data. It has been found that the mean free volumes radii are in the investigated region of plasticizer concentrations a linear function of the concentration of the dioctyl phthalate in the PVC. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 26
    ISSN: 0959-8103
    Schlagwort(e): miscible blends ; polyesters ; positron annihilation lifetime spectroscopy ; free volume ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Four blend systems (miscible binary polyester blends) have been examined by positron annihilation lifetime spectroscopy (PALS). The ortho-Positronium pick off lifetime, τ3, is related to the mean free volume cavity size in these miscible blends. The measured free volume cavity size for the blends is compared to the size predicted from linear additivity of the homopolymers. A negative deviation from linear additivity is observed for τ3 in each of the blend systems, and this behaviour is interpreted as a contraction of the mean free volume cavity size due to the changes in molecular packing that occur on blending. The consequence of these free volume results for the mechanical properties of miscible polyester blends is discussed and tested for the polycarbonate/Kodar system. The glass transition data suggest weak specific interactions in the blends; however, the mechanical properties are significantly affected by blending.
    Zusätzliches Material: 14 Ill.
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  • 27
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 18-27 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Solid-catalyzed copolymerization reactions of ethylene and α-olefins can produce complex mixtures generally regarded as “polyethylenes” (including linear low-density polyethylene). The selective nature of those catalysts can lead to block-like character in segments of polymer molecules, and these segments are sufficiently dissimilar (from a thermodynamic viewpoint) to allow for the possibility of microphase separation in the melt. Such a molecular-level phase separation would substantially alter the melt rheology, the crystallization process, and hence the mechanical and optical properties of the resulting product. It would, in principle, be identical to those occurring in conventional well-defined block copolymers, allowing the thermodynamic models developed for those systems to be extended to block-like polyolefins.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 28
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 52-63 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Relationships between the rheological, morphological, and tensile properties of an immiscible blend of 25 wt% of a thermotropic liquid crystalline polymer (LCP) with polycarbonate are presented. The shear viscosity of the blend is intermediate between the two constituent materials, and indicates immiscibility in the melt. Extrudate swell behavior is examined and found to be closely related to that of polycarbonate. The morphology of the dispersed LCP phase varies between droplets and oriented fibrils, and is highly correlated with changes in tensile properties. Fibrils are associated with increased tensile modulus, and their development is favored in the elongation flow fields present in the spinline and in the die convergence section. In all cases, blend stiffness is less than that predicted for a continuous fiber-reinforced composite. Enhanced tensile modulus is associated with both extrusion from shorter length dies and increases in spinline draw ratio, with the latter proving the most important in fibril formation.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 29
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 79-91 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: During the last few years, improvements in control strategies became a necessity, with controls being targeted on material properties. The ever-increasing demand for polymer blends spells the need for in-line instrumentation capable of monitoring blend properties such as morphology. Since ultrasonics have proved to be sensitive to properties of multiphase materials, their performance for discriminating blend morphology was explored here. In-line and off-line (static, with no flow) ultrasonic measurements were made on different blends of polystyrene (PS), polyethylene (PE), and polypropylene (PP) for various viscosity ratios, and over the entire range of composition. Blends were compounded on a ZSK-30 Werner & Pfleiderer intermeshing co-rotating twin-screw extruder. In-line ultrasonic measurements were performed on both single-screw and twin-screw extruders. Ultrasonic properties (velocity and attenuation) were found to vary approximately linearly with composition. Mixing rules were evaluated for the description of ultrasonic behavior. For the attenuation measurements, the positive deviations from these rules were found significant. The additional attenuation was attributed to scattering generated by the presence of the minor phase inclusions.
    Zusätzliches Material: 23 Ill.
    Materialart: Digitale Medien
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  • 30
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 92-99 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The phase behavior of polymer blends under simple shear flow has been studied using a custom-designed rheo-optical system consisting of a two-dimensional small-angle light scattering (SALS) device incorporated into a conventional rheometer. Two-dimensional SALS images were gathered for model polymer blend systems with different quiescent phase behavior: polystyrene/polyisobutylene (PS/PIB) that exhibits upper critical solution temperature phase behavior and polystyrene/poly(vinyl methyl ether) (PS/PVME) that shows lower critical solution temperature phase behavior. For the PS/PIB blend, shear-induced phase mixing occurred at a critical shear rate. Below that critical shear rate, the dispersed phase was highly elongated parallel to the flow direction. For PS/PVME blends, a streak scattering pattern was observed even though the sample became optically clear after shearing. We observed, apparently for the first time, the development of a bright-streak pattern from a transient dark-streak pattern for a polymer blend system under shear. Rheo-microscopy studies revealed an intriguing wave pattern that developed coincident with the observation of a streak pattern by SALS. The relationship between the two phenomena has not yet been established.
    Zusätzliches Material: 7 Ill.
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  • 31
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The dispersions of both reactive and nonreactive polymer-polymer blend systems achieved in three different mixers are compared. The dispersions are prepared using an industrial scale twin-screw extruder, a laboratory internal mixer, and a miniature cup and rotor mixer. The morphology development in the three mixers is remarkably similar: The dispersed phase is stretched into sheets and ribbons; these sheets and ribbons then break into cylinders, which subsequently break into droplets via Rayleigh-type instabilities. Drop size distributions can be accurately predicted if we know the size of cylinders formed in the high shear fields of the mixer. There is a significant effect of quenching time on blend morphology - i.e, to properly evaluate mixing, blends must be quenched extremely quickly (well within a minute). Otherwise, we need to consider the morphology development during the quenching time, which may not be relevant to the mixing. There is a uniform shear stress in the miniature mixer, unlike the other mixers, which have varying stress levels. It is shown that a high stress level followed by a lower stress level is required in polymer blending to achieve efficient mixing. In the high stress level, the dispersed phase is stretched into extended shapes, which undergo instabilities and break up upon entering the low stress level. In the miniature mixer, the dispersed phase sees only one stress level, and thus very extended shapes persist at the end of mixing. The final dispersions in the twinscrew extruder and internal mixer at matched maximum shear rates are almost identical. For similar shear rates in the miniature mixer, the final dispersion of reactive blends is comparable to the other mixers. However, the miniature mixer does a poor job in dispersing high viscosity uncompatibilized blends, and the mixing conditions must be altered to obtain efficient mixing.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 32
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 129-136 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Instrumented impact testing and analysis were performed on an interlaminartoughened carbon fiber epoxy composite (Toray 3900-2/T800H) and a conventional (untoughened) epoxy composite (Fiberite 934/T300). Severity of impact was varied by using a wide range of impact energy. The effect of difference in the tup of the impact instrument was discussed. The residual compressive strengths after compact (CAI's) were measured by using a universal mechanical tester. The impact damage and delamination resistance of the toughened and conventional composites were quantitatively compared. At the same impact energy, the extent of damage was much less severe and the CAI was higher for the toughened composite. Relationships between the CAI's, the state of impact damage, and impact energy were investigated. Impact damage mechanisms for these two composites were not exactly the same. The impact damage of the conventional composite exhibited much greater extents of delamination. By contrast, interlaminar delamination in the toughened composite was found to be significantly suppressed, and the impact damage was more dominated by controlled matrix cracking/fiber damage, instead of catastrophic delamination. As a result, the CAI's of the toughened composite exhibited a monotonous decrease with increase in the impact energy and in the linear dimension of extents of damage.
    Zusätzliches Material: 9 Ill.
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  • 33
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 151-156 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Thermal diffusivity of high density polyethylene (HDPE) was studied over a wide range of temperatures (25 to 200°C) by melting powdered HDPE in a cylindrical mold at several pressures (101.3 to 5065 KPa gage) and recording the temperature profiles at several radial positions. The energy equation was solved numerically for cylindrical geometry. The thermal diffusivity of HDPE was fit as a function of temperature, porosity, and pressure.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 34
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 170-172 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: This communication is a theoretical re-examination of the model proposed by Choe and Lee for the nonisothermal crystallization kinetics of semicrystalline polymers.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 35
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 180-183 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Halogenophenol novolac (HPN)-based negative resists exhibit excellent sensitivity and pattern resolution properties. The HPNs act as synergists for crosslinking with other irradiation labile compounds such as naphthoquinone diazide and bisazide vs. hydrogen halide (HX) elimination reaction, resulting in additional crosslinking, probably by aryl radical recombination and/or addition. We describe a new resist formulation based on HPN binder and melamine crosslinker (Cymel 303). In this case the irradiation induced HX elimination additionally catalyzes the melamine crosslinking.
    Zusätzliches Material: 2 Ill.
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  • 36
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 173-179 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The orientational drawing of films from different thermoplastics has been studied. The value of the activation energy of drawing in the regions of forced elasticity (necking), high elasticity, and viscous flow (ΔE1, ΔE2, ΔE3) has been found to vary directly with the activation energy for viscous flow of the melt (ΔEη). Here ΔE1 〈 ΔE2 〈 ΔE3 = ΔEη. Thus Δ Eη characterizes the potential of thermoplastics for orientational drawing under different deformation conditions, since it reflects simultaneously both the intermolecular interaction level and chain flexibility. For maximum chain orientation, the calculated values for the change in the entropy are close to that of the entropy change during crystallization (melting) of the same polymer. The deformation of polymer may be described as a deformation of an entanglement network from the standpoint of classic elasticity theory. Some parameters for an entanglement network were calculated from the results of the drawing experiments. The density of the entanglement network (DEN) depend on the polymer composition: For flexible-chain polymers the DEN is less, for rigid-chain polymers (with coiled chains) it is higher. The DEN affects the maximum (prebreak) drawing ratio: The greater the DEN, the smaller the ratio to which a film can be drawn. At high orientation, the tensile strength of different polymer films tend to be similar, if drawing is not accompanied by crazing.
    Zusätzliches Material: 8 Ill.
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  • 37
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 190-194 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The block copolyetheresters with hard segments of poly(butylene terephthalate) and soft segments of poly(tetramethylene ether) were prepared by a terephthalic acid (TPA) process in the presence of some salts. The preparations of a block copolyetherester under various conditions were first studied in a 1 L stainless steel reactor to find the best method. Then, the preparations of four block copolyetheresters were run in a pilot plant comprising a 200 L polyesterification reactor and a 200 L polymerization reactor under the suitable condition. The presence of some salts reduced the formation of tetrahydrofuran (THF), and also reduced the total reaction time in the pilot plant. The thermal properties and various mechanical properties of the block copolytheresters prepared by the pilot plant were investigated to evaluate the feasibility of this method.
    Zusätzliches Material: 4 Ill.
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  • 38
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 144-150 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The objective of the current paper was to extend the relationships between complex polymer structures and microwave absorptivity that were formulated in the first three papers of this series (1-3). The microwave processing of composite and polymeric blends via a cylindrical resonance wave cavity and a rectangular standing wave applicator is described. These polymeric materials were irradiated in a low power (〈 100W) electric field at 2.45 GHz. Graphite-epoxy laminates were processed in both standing and traveling wave applicators. Rapid heating and curing were achieved in both cases. An observation of significance was that, with proper tuning of the traveling wave device (the precursor of a protable repair tool), it proved to be highly effective in processing. Additionally, a compatible blend of poly(methyl methacrylate) and poly(vinylidene fluoride) was heated in and applicator and the rates of temperature rise were demonstrated to depend upon morphology.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 39
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Mechanical properties of polymers can be described by their stress/strain curves and by their behavior under dynamic mechanical thermal analysis (DMTA). The purpose of this paper is to report such mechanical properties for two unsaturated polycarbosilanes: poly(1, 1-dimethyl-1-sila-cis-pent-3-ene) (I) and poly(1-methyl-1-phenyl-1-sila-cis-pent-3-ene) (II). Tensile strength, elongation at break, modulus, bending modulus, Tg, and tan δ for I, II and for sulfur crosslinked I and II have been measured. The influence of polymer molecular weight, quantity of crosslinking agent, cure time, presence of carbon black filler, the effect of crosshead speed, and frequency on these properties was investigated.
    Zusätzliches Material: 11 Ill.
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  • 40
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 165-169 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The effects of physical aging on the failure behavior of a typical brittle polymer, polystyrene, have been studied. Properties examined were creep rupture lifetimes, fatigue lifetimes, and environmental stress cracking in ethanol. Fractured samples were examined both optically and by scanning electron microscopy to determine the degree of crazing. It was found that a longer physical aging time produced shorter lifetimes in all cases. The main reason for this is the reduction in craze strength caused by a reduced toughness due to physical aging. A long aging time was found to delay craze formation, but once formed, these crazes were much less stable than those formed with a short aging time. The effects of aging are important on failure prediction criteria and on testing methodologies, and the implications are discussed.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 41
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 184-189 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Dielectric and rheological measurements are reported for the cure in a series of mixtures of an epoxy-acrylate with n-butyl methacrylate. The level of the initiator and properties of the epoxy acrylate and n-butyl methacrylate influence the cure characteristics and morphology of the film formed. Analysis of the rheological data indicates that during the curing process, microphase separation occurs within the mixture. The changes in the dielectric relaxation behavior with composition of the completely cured material is also consistent with microphase separation occurring in these resins while they are cured.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 42
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 195-201 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Using low conversion bulk copolymerization experimental data and the apparent rate constant model, the monomer chain cross-transfer rate constants and the cross-termination coefficient were evaluated. It was found that the dependence of the cross-termination coefficient on composition is a function of initiator efficiency and that monomer chain cross-transfer rate constant are relevant for the theoretical estimation of the molecular weights and molecular weight distributions.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 43
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 202-210 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The melt viscosity of thermoplastic starch has been investigated as a function of temperature, moisture content, and processing conditions. The effects of various low molecular weight additives have also been studied. Starch melts exhibit power law behavior over the range of shear rates studied. Melt viscosity decreased with increasing temperature and moisture content (MC). The power law index m increased with increasing temperature. The consistency K decreased with increasing temperature and increasing moisture content. Moisture content during the pelletizing step influenced melt viscosities measured after equilibration to different MCs. All additives studied except glycerol monostearate (GMS) significantly lowered the melt viscosity of starch, some more effectively than water relative to starch with 15% MC. Starch with GMS had viscosities essentially the same as, or slightly higher than, starch/water. This behavior may be due to the presence of unmelted helical inclusion complexes of starch and GMS. Starch formulations at 160°C exhibited melt visocosities similar to an LDPE of melt index 1.8.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 44
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 289-290 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 45
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 291-303 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The phenomenology of yield in bisphenol-A polycarbonate is explored through tensile tests on thin rectangular specimens and through pressure-induced bulging of thin, clamped circular disks. In a tensile test, while the nominal critical stress at which yield initiates and the nominal draw stress at which a stable neck propagates along a specimen depend on the temperature and the strain rate, the ratio of the draw stress to the critical stress is shown to be approximately 0.75 over a temperature range of 22 to 65°C and strain-rates in the range of 10-4 to 100 s-1. Specimens subjected to constant tensile loads between the draw and critical stresses are shown first to creep till stretches on the order of 1.06 are attained and then are shown to undergo stable necking. Tensile tests on thin, wide rectangular specimens show that yielding initiates through shear bands that broaden and intersect to generate necks, which subsequently propagate along the specimen. In pressure-induced bulging of clamped disks, biaxial stretching progresses monotonically under increasing pressures; strain localization does occur near the outer edges of the specimens, however. Heating of a specimen with a substantial stably necked region shows that the temperature-induced recovery of the specimen from its deformed state begins well below the transition temperature Tg of the material, although most of the recovery occurs at Tg.
    Zusätzliches Material: 19 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 46
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 317-330 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Samples of poly(etherether ketone) (PEEK) were subjected to large plastic deformations under uniaxial tension and simple shear by means of a new video-controlled testing method at constant true strain rate. The “equivalent” stress-strain curves obtained under the two loading modes are close at the yield point, but diverge drastically at large strains, with a rapidly increasing hardening in tension and a moderate hardening under simple shear. X-ray diffraction goniometry shows that these contrasting behaviors are associated with the different textures developed in the crystallite orientations. Under tension, the PEEK lamellae are progressively tilted in such a way that the chain axis becomes oriented parallel to the tensile axis; in the other mode, the final chain orientation is near to the shear axis. DSC analyses of deformed samples in both modes are carried out. The results show that the tension loading induces a fragmentation of the thin lamellae, while the shear mode generates less fragmentation. A quantitative model is presented that involves a composite approach: (i) the viscoplastic deformation of the crystalline lamellae, which is controlled by chain slip and transverse slip systems on planes parallel to the c axis, and (ii) the hyperelastic deformation of the amorphous phase, which depends on the affine unfolding of statistically distributed subchains. A discussion of the influence of the CRSS values on the stress-strain curves and textures is developed by means of this model.
    Zusätzliches Material: 19 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 47
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 345-350 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A constitutive equation for nonlinear viscoelasticity is used to model the mechanical response of solid polymers such as polycarbonate. The nonlinearity arises from a reduced time which causes stress relaxation to accelerate with increasing strain. The constitutive equation can account for the occurrence of yield in a homogeneous uniaxial constant strain rate test. The constitutive equation is used in a study of the pure bending of beams. It is assumed that the classical assumption of beam theory is valid, i.e., plane sections remains plane. At each fixed time, the strains vary linearly through the depth of the beam. At a fixed material element the strain varies in time with the curvature. This spatial variation of the strains combined with the nonlinear dependence of the reduced time on strain leads to a significantly different response from that given by traditional beam theory. The implications of this for the bending moment history, stress distributions, and other factors that relate to beam design are discussed.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 48
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995) 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 49
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 385-386 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 50
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 403-410 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Aging experiments using the NIST (National Institute of Standards and Technology) torsional dilatometer have been performed in which the temperature of an isothermally equilibrated epoxy glass was abruptly changed to a new temperature T0 and the evolution of the volume and torsional relaxation responses recorded. The results of down-jump and up-jump experiments were found to differ dramatically. Not only is the normal asymmetry of volume approach to equilibrium found, but the mechanical responses are found to evolve differently from the volume response, contrary to simple free volume models of the physical aging process. It is found that the torsional modulus changes with increasing time after the T-jump. In the case of the down-jump the evolution of the modulus ceases prior to that of the volume of the sample. In the up-jump experiment, the contrary is true, viz., the modulus continues to evolve after the volume has attained its equilibrium value. The implications of this for the description of material behavior are discussed.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 51
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 395-402 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The statistical theory of the birefringence of an individual non-Gaussian elastomer chain is used together with a chain network description of rubber elasticity to develop a relationship among the strain, birefringence, and stress in elastomers, valid for large deformations under generalized strain states. The result is a fully three-dimensional internal variable based constitutive model of rubber elasticity in which measurement of the elastomeric birefringence during straining in one deformation state characterizes the optically anisotropic response of the elastomer. Simultaneous measurement of the stress vs. strain response provides the rubbery modulus and limiting network extensibility properties needed to completely characterize the mechanical anisotropy of the material. Once characterized using the single, large deformation experiment, the birefringence and stress responses of the elastomer in other deformation states may then be predicted without adjusting any model parameters. The theory is compared to experimental studies from the literature of large strain deformations of elastomers in uniaxial tension and compression for which the exhibited birefringence and stress responses of deforming elastomers have been simultaneously recorded.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 52
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 387-394 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Rigid, closed-cell, polyurethane foam consists of interconnected polyurethane plates that form cells. When this foam is compressed, it exhibits an initial elastic regime, which is followed by a plateau regime in which the load required to compress the foam remains nearly constant. In the plateau regime, cell walls are damaged and large permanent volume changes are generated. As additional load is applied, cell walls are compressed against neighboring cell walls, and the stiffness of the foam increases and approaches a value equal to that of solid poyurethane. When the foam is loaded in tension, the cell walls are damaged and the foam fractures. A constitutive theory for rigid polyurethane foam has been developed. This theory is based on a decomposition of the foam in two parts: a skeleton and a nonlinear elastic continuum in parallel. The skeleton accounts for the foam behavior in the elastic and plateau regimes and is described using a coupled plasticity with continuum damage theory. The nonlinear elastic continuum accounts for the lock-up of the foam due to internal gas pressure and cell wall interactions. This new constitutive theory has been implemented in both static and dynamic finite element codes. Numerical simulations performed using the new constitutive theory are presented.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 53
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 426-431 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The nonlinear fracture behavior of polycarbonate is investigated. The feasibility of measurement of the J integral through the optical method of reflected caustics is demonstrated. Significant increase in the crack growth resistance during small amounts of crack extension is observed.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 54
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995) 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 55
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 432-440 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Microllular plastics are cellular polymers characterized by cell densities greater than 109 cells/cm3 and cells smaller than 10 μm. One of the critical steps in the continuous production of microcellular plastics is the promotion of high cell nucleation rates in a flowing polymer matrix. These high nucleation rates can be achieved by first forming a polymer/gas solution followed by rapidly decreasing the solubility of gas in the polymer. Since, in the processing range of interest, the gas solubility in the polymer decreases as the pressure decreases, a rapid pressure drop element, consisting of a nozzle, has been employed as a continuous microcellular nucleation device. In this paper, the effects of the pressure drop rate on the nucleation of cells and the cell density are discussed. The experimental results indicate that both the magnitude and the cell density are discussed. The experimental results indicate that both the magnitude and the rate of pressure drop play a strong role in microcellular processing. The pressure phenomenon affects the thermodynamic instability induced in the polymer/gas solution and the competition between cell nucleation and growth.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 56
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 441-459 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The steady melting of several amorphous and semicrystalline polymers during spin welding is analyzed by solving a simplified set of momentum and energy balance equations, assuming a shear-rate and temperature-dependent viscosity. A numerical model is developed for predicting the flow field and the temperature distribution in the molten film. It is shown that the steady melting rate of the thermoplastic solid is affected by the variable viscosity, by the pressure applied on the parts to be joined, and by a balance between the viscous heat generation in the melt and the convection of colder material into the molten film. The convection of heat in the outflow direction is shown to have a much smaller effect on the melting process.
    Zusätzliches Material: 21 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 57
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 477-482 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Glassy shell-rubbery core polymer particles, 0.1 to 0.2 μm in diameter, increase the plane strain JIC values of 3.175 mm thick polycarbonate from 3.05 kJ/m2 (no particles) to 9.5 kJ/m2 (7.5 phr particles) at 23°C. Some modest decreases in these values are caused by tests at -20°C in samples 9.525 and 3.175 mm thick. If only the particle concentration is varied, JIC increases monotonically to 7.5 phr (by wt), then levels off or decreases slightly at 10.0 phr. The total volume of 1 to 2 μm diameter cavities formed in the matrix by the apparently unbonded particles behaves similarly; cavity volume and JIC are directly related. With increasing particle concentration the tensile modulus is unchanged, the yield stress and strain decrease modestly, the strain at fracture decreases appreciably, and the heat recoverable orientation in the fractured samples decreases. Few cavities are formed. The particles reduce the extent of shear deformation in the tensile samples.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 58
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 483-492 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A mathematical model for a laser-induced photopolymerization process has been developed. This model simulates important aspects of stereolithography, a rapid prototyping process used for the production of three-dimensional plastic parts. The model consists of a set of coupled partial differential equations and considers irradiation, chemical reaction, and heat transfer in a small zone of material exposed to a stationary UV laser source. Numerical techniques are used for an approximate solution of the model equations, and the output includes spatial and temporal variations in the conversion of monomer to polymer, depletion of photoinitiator, and local variations of temperature in and around the region contacted by the laser light. Maximum conversions of approximately 60% and peak temperature rises of approximately 35° C were calculated for the cylindrical exposed region. Results have provided insights concerning laser dwell time, depth penetration, and the uniformity of polymer formed during the stereolithography process.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 59
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 499-505 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The deformation of three types of sulfone polymers - polysulfone (PSF), poly(ether sulfone) (PESF), and polyarylsulfone (PASF) - was performed with a mechanical testing system (MTS). The result and samples were studied using a transmission electron microscope (TEM), a dynamic mechanical analyzer (DMA), and a dielectric thermal analyzer (DETA). Stripes on TEM micrographs for small deformations increase with the fracture toughness (GIc). The activation energy (Ea) of the α-transition was determined from DETA. The results show that both Ea and TEM micrographs can be used to qualitatively estimate the order of GIc of sulfone polymers. An energy model was proposed to explain this phenomenon.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 60
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 419-425 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: We investigate criteria for craze failure at a crack tip and the dependence of craze failure on the molecular weight of the polymer. Our micromechanics model is based on the presence of cross-tie fibrils in the craze microstructure. These cross-tie fibrils give the craze some small lateral load bearing capacity so that they can transfer stress between the main fibrils. This load transfer mechanism allows the normal stress on the fibrils directly ahead of the crack tip in the center of the craze to reach the breaking stress of the polymer chains. We solve for stress field near the crack trip and use it to relate craze failure to the external loading and microstructural quantities such as the craze widening (drawing) stress, the fibril spacing, the molecular weight, and the force to break a single polymer chain. The relationship between energy flow to the crack tip due to external loading and the work of local fracture by fibril breakdown is also obtained. Our analysis shows that the normal stress acting on the fibrils at the crack tip increases linearly as the square root of the craze thickness, assuming that the normal stress distribution is uniform and is equal to the drawing stress acting on the craze-bulk interface. The critical crack opening displacement, and hence the fracture toghness is shown to be proportional to [1-(Me/qMn)]2, where Me is the entanglement molecular weight, Mn is the number average molecular weight of polymer before crazing, and q is the fraction of entangled strands that do not undergo chain scission in forming the craze.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 61
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 471-476 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The JIC values for core-shell-particle-toughened polycarbonate were determined at different temperatures and at 0, 2.5, 5.0, 7.5, and 10.0 phr particle content by six similar methods, using compact tensile specimens. At the 2.5 phr toughener level, the JIC values ranged from 2878 to 6100 J/m2, and at 7.5 phr, they ranged from 6125 to 10,760 J/m2, dependent only upon how the same JI-Δ a data were interpreted. This indicates that more work will be required before a reliable method of JIC measurement that can be applied to tough polymers is achieved.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 62
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 461-470 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Stoichimetric mixtures of a diglycidyl ether of bisphenol A (DGEBA)/ diaminodiphenyl sulfone (DDS) and a DGEBA/meta phenylene diamine (mPDA) were cured using both microwave and thermal energy. Fourier transform infrared (FTIR) was used for the measurement of the extent of cure and thermal mechanical analysis (TMA) was used for the determination of the glass transition temperature (Tg). The cure kinetics of the DGEBA/mPDA and DGEBA/DDS systems were described by an autocatalytic kinetic model up to vitrification in both the microwave and thermal cure. For the DGEBA/mPDA system, the reaction rate constants of the primary amine-epoxy reaction are equal to those of the secondary amine-epoxy reaction, and the etherification reaction is negligible for both microwave and thermal cure. For the DGEBA/DDS system, the reaction rate constants of the primary amine-epoxy reaction are greater than those of the secondary amine-epoxy reaction and the etherification reaction is only negligible at low cure temperatures for both microwave and thermal cure. Microwave radiation decreases the reaction rate constant ratio of the secondary amine-epoxy reaction to the primary amine-epxy reaction and the ratio of the etherification reaction to the primary amine-epoxy reaction. Tg data were fitted to the DiBenedetto model. A master curve and a time-temperature-transformation (TTT) diagram were constructed. The vitrification time is shorter in microwave cure than in thermal cure, especially at higher isothermal cure temperatures. For the DGEBA/mPDA system, the minimum vitrification time is two to five times shorter in the microwave cure than in the thermal cure. For the DGEBA/DDS system, the minimum vitrification time is 44 times shorter in the microwave cure than in the thermal cure.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 63
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 493-498 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A mathematical process model that stimulates important aspects of stereolithography, a rapid prototyping technique used for the production of three-dimensional plastic parts, has been developed. The model consists of a set of coupled partial differential equations and considers irradiation, chemical reaction, and heat transfer in a vat of photomonomer exposed to a moving UV laser source. Laser motion occurs in a straight line (vector path), and the model thus simulates the production of a single strand of plastic. Numerical techniques are used for approximate solution of the model equations, and output includes spatial and temporal variations in conversion of monomer to polymer, depletion of photoinitiator, and variations of temperature along the line of exposed material. The formation of a temperature wave that moves along the line of plastic is observed, together with the fact that the leading edge of the wave is steeper than the trailing edge, i.e., the material heats considerably faster than it cools. The maximum temperature of the wave reaches a pseudo-steady state after a short time. The results have provided useful information concerning the temperature at which the majority of the polymerization occurs; provided information on overall transient temperature behavior; allowed computer prediction of stereolithography working curves (cure depth and cure width vs. laser scan rate); and afforded a means for evaluating the amount of reaction that occurs in the dark period after light exposure.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 64
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The linear viscoelastic behavior of commercial broad-distribution polypropylenes is studied. The samples underwent different controlled peroxide degradation rates, so they exhibit different molecular distributions. The relaxation spectrum is obtained by assuming that it takes the shape of a Log-Normal distribution. It is in agreement with the linear viscoelasticity theory by providing limiting values, contrary to other models. Moreover, the ratio τw/τn which takes place in this law is very useful to distinguish the synthesis differences of the samples when the Melt Flow Index alone cannot.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 65
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 546-554 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The creep characteristics of polycarbonate at elevated temperatures are investigated. The onset of glass transition temperature of polycarbonate is determined. An Arrhenius type relationship is used to describe the creep process and the concept of property retention index as applied to creep is discussed. An attempt is made to construct the master rupture curves for polycarbonate. The onset of glass transition temperature of polycarbonate was placed at around 110°C. It is concluded that the Arrhenius theory and the concept of property retention index are extremely useful in the construction of master rupture curves and that they require further investigation.
    Zusätzliches Material: 21 Ill.
    Materialart: Digitale Medien
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  • 66
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 538-545 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Blends of poly(ethylene 2,6-naphthalate) (PEN) and a liquid crystalline copolyester (LCP), poly(benzoate-naphthoate), were prepared in a twin-screw extruder. Specimens for mechanical testing were prepared by injection molding. The morphology and mechanical properties were investigated by scanning electron microscopy (SEM) and an Instron tensile tester. SEM studies revealed that finely dispersed spherical domains of the liquid crystalline polymer (LCP) were formed in the PEN matrix, and the inclusions were deformed into fibrils from the spherical droplets with increasing LCP content. The morphology of the blends was found to be affected by their composition and a distinct skin-core morphology was found to develop in the injection molded samples of these blends. Mechanical properties were improved with increasing LCP content, and synergistic effects have been observed at 70 wt% LCP content whereas the elongation at break was found to be reduced drastically above 10 wt% of LCP content. This is a characteristic typical of chopped-fiber-filled composites. The improvement in mechanical properties is likely due to the reinforcement of the PEN matrix by the fibrous LCP phase as observed by scanning electron microscopy. The tensile and modulus mechanical behavior of the LCP/PEN blends was very similar to those of the polymeric composite, and the tensile strength and flexural modulus of the LCP/PEN 70/30 blend were two times the value of PEN homopolymer and exceeded those of pure LCP, suggesting LCP acts as a reinforcing agent in the blends.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 67
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 557-563 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The coefficient of dynamic friction is often the controlling factor for solids conveying, pressure generation, and thermal decomposition of a resin in the feed section of a single-screw plasticating extruder. The coefficients of friction are, however, very poorly understood, and the interpretation of the measurements are complicated by the dissipation of frictional energy at the sliding interface. A new instrument was recently built to help understand dynamic friction, and a numerical technique was developed to estimate the interface temperture. Coefficients of dynamic friction for several polyethylene resins are presented in this paper as a function of the surface temperature, pressure, and velocity. The relationship of the data with respect to the extrusion process is discussed.
    Zusätzliches Material: 19 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 68
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 577-586 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A one-dimensional flow model for non-Newtonian liquids inside a dual-cavity slot die is presented. The model is capable of analyzing slot dies of any cavity shape, cavity taper, slot-length variations, and slot-gap variations. The proposed model incorporates a truncated-power-law model for the viscosity of non-Newtonian liquids. According to flow models with power-law approximation for liquid viscosity, the distribution of non-Newtonian liquid through a slot die depends on the slot Reynolds number only. With our model, we find that the zero shear viscosity and the relaxation time of a non-Newtonian liquid have large effects on its distribution. For non-Newtonian liquids which are expected to experience shear-thinning over portion of a slot die, it is concluded that a flow model with a truncated-power-law approximation for liquid viscosity be used to predict the liquid distribution from the die.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 69
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 598-603 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: This paper deals with the residence time distribution (RTD) in a non-intermeshing counter rotating twin screw extruder.The RTDs were measured in three vent zones of the extruder sparately, and in the adjacent zones combined, using a soluble dye as the tracer. Assuming that the RTDs in the adjacent zones are independent of each other, the overall RTD was also calculated using a previously developed statistical theory. The theory has also confirmed the consistency of the present measurements.A predictive RTD model for the non-intermeshing twin screw extruder, based on the flow analysis of the individual screw zones and their statistical superposition, was also developed. The predictions are in good agreement with experiment.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 70
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 619-636 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The flow-induced phase morphological development under different extrusion conditions was studied in terms of the rheological property and interfacial tension of various elastomers and thermoplstics. The interfacial tension for elastomers and thermoplastics was investigated by using a breaking thread method (1-4). We found that the method is suitable for measuring interfacial tension without degradation. The droplet-fibrillation transition phenomenon was observed in various extrudates of fluoroelastomer/polycarbonate blends. The criteria for the flow-induced morphology, in particular the droplet-fibrillation transition, are critically discussed in this paper.
    Zusätzliches Material: 23 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 71
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 637-641 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Results of measurements of the electrical conductivity of low density polyethylene/polypyrrole and polystyrene/polypyrrole composites are reported. It is observed that the electrical conductivity of the composite vs. concentration follows the power law predicted by the percolation theory. The manufacturing process influences the homogeneity of the composite at microscopic scale and thus the percolation threshold. Annealing studies show that the stability of the electrical conductivity of the composite is related to the thermal expansion of the polymers and the relaxation of the polymer chains. The decrease of the electrical conductivity of the composite is attributed to the interruption of the percolation path.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 72
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 648-657 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The compatibilizing effect of a polystyrene-hydrolyzed poly(t-butyl acrylate) diblock copolymer (SBAH) on the phase structure, rheological properties, and mechanical properties of immiscible poly(2,6-dimethyl-1,4-phenylene ether) (PPE) and polyamide-6 (PA) blends was investigated. The SBAH was prepared by sequential anionic polymerization of styrene and t-butyl acrylate, followed by acid-catalyzed hydrolysis of t-butyl acrylate block. Scanning electron micrographs show that the blends exhibit a more regular and finer dispersion when the SBAH of 47% hydrolyzed t-butyl acrylate block is added. By addition of small amount of the block copolymer, the blends show non-Newtonian power-law behavior, and the contribution of storage modulus (G′) to the total response increases. Solubility tests support the formation of graft copolymer by chemical reaction between amine groups of the PA and carboxyl groups of the SBAH. Both modulus and strength are improved about 20% with addition of the 3 wt% SBAH, while the elongation at break decreases notably; thus, the blends fail in a brittle manner.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 73
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 666-672 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The peel force of a PVDF/3-APS/Si joint and a PVDF/3-APS/Al joint can reach the same level by treating the Si substrate with ≥ 0.3% 3-aminopropyltriethoxy silane (3-APS) solution and treating the aluminum substrate with NH3 solution (pH 10.5) first and then with ≥ 3% 3-APS solution. Scanning electron micrographs show that the interfacial adhesion mechanisms of PVDF/3-APS/Si joints and PVDF/3-APS/Al joints are different. In the peel test, the PVDF [poly(vinylidene fluoride)] break surfaces from PVDF/3-APS/Si joints reveal striations on the surface and less plastic deformation. The significant plastic deformation of the PVDF at the break surface may result from the deeper interpenetration of 3-APS with PVDF in the PVDF/3-APS/Al joint than in the PVDF/3-APS/Si joint. The peel force of PVDF film/substrate joint depends on many factors: film thickness, peel rate, concentration of coupling agent, the treatment time of the coupling agent on the substrate, and the substrate pretreatment.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 74
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 693-702 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The morphologies of amorphous polymer blends produced by extrusion were investigated by transmission electron microscopy. Polymers with similar viscosities, i.e. poly(methyl methacrylate) (PMMA), polystyrene (PS), and random copolymers P(SxMMA1 - x) were mixed pairwise, in different compositions. Finely dispersed phase structures were produced in the blends, with domains in the submicron range. The structure patterns were considerably perturbed by the stress fields in the extruder. Domain-matrix and co-continuous morphologies were obtained, in a distribution controlled mainly by the viscosity ratio. Annealing after extrusion led to structure coarsening, whereby the patterns were changed until a steady state was established. Sometimes, matrix inversion was observed.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 75
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 680-692 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Morphology and oxygen permeability studies were carried out for blends of poly(ethylene terephthalate), PET, and poly(ethylene 2,6-naphthalate), PEN, with poly(ethylene-co-vinyl alcohol), EVOH. PET/EVOH blends are seen as a possible substitute for poly(vinylidene chloride)-coated PET packaging films. The effects of several processing parameters such as draw temperature and draw ratio on blend morphology and barrier properties suggest that the morphology of the EVOH phase dictates to a large extent the oxygen permeabilities of these blends. The relationships between morphology and oxygen permeability and explained are explained by consideration of two-phase conduction models. The model of Fricke is found to be a good predictor of the barrier properties of the PET/EVOH system. The oxygen permeability of PET was reduced by a factor of 4.2 with the addition of 20 wt% EVOH and that of PEN by a factor of 2.7 with the addition of 15 wt% EVOH. Water vapor permeabilities and mechanical properties of PET and PEN were only slightly affected by the addition of 15 wt% EVOH.
    Zusätzliches Material: 18 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 76
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995) 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 77
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 722-730 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A modified acetone process for the preparation of aqueous polyurethane (PU) dispersion is investigated. PU dispersions were prepared by polyaddition of isophorone diisocyanate (IPDI) to poly(tetramethylene ether glycol) (PTMG) and dimethylolpropionic acid (DMPA), followed by neutralization of pendant COOH groups with triethylamine (TEA). The resulting prepolymer chain was then extended through reaction with an ethylenediamine (EDA) derivative bearing sulfonate groups. The effect of such preparation conditions as catalyst (dibutyltin dilaurate, DBTDL) concentration, the acetone/PU ratio, phase-inversion temperature, agitation rate, and water-addition rate on the average particle size of aqueous PU anionomer dispersions is systematically studied using fractional factorial design and response surface methodology. Fractional factorial analysis indicates that the effects of the acetone/PU ratio, phase-inversion temperature, water-addition rate as well as the two factor interactions of DBTDL concentration and phase-inversion temperature, of the acetone/PU ratio and phase-inversion temperature, and of acetone/PU ratio and agitation rate are the key variables influencing average particle size of PU dispersions. Empirical models for average particle size are fitted and plotted using central composite experimental design as contour diagrams in order to facilitate examination of the average particle size results. The results show that for a 100 g PU anionomer containing 0.311 wt % COOH and 1.51 wt % SO3H groups, a minimum number-average particle size of the dispersion ∼ 25 nm can be obtained under an acetone/PU ratio, water-addition rate, phase-inversion temperature, catalyst concentration, and agitation rate of 3.65, 2 mL/min, 50°C, 150 ppm and 350 rpm, respectively.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 78
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 733-740 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Nonisothermal crystallization kinetic data obtained from differential scanning calorimetry (DSC) for a poly(ethylene terephthalate) are corrected for the effects of temperature lag between the DSC sample and furnace using the method of Eder and Janeschitz-Kriegl which is based on experimental data alone without resort to any kinetic model. A method is presented for shifting the corrected nonisothermal crystallization kinetic data with respect to an arbitrarily chosen reference temperature to obtain a master curve. The method is based on experimental data alone without reference to any specific form of kinetic model. When the isothermal crystallization kinetic data for the same material are shifted with respect to the same reference temperature, a master curve is also obtained which overlaps to a large extent the corresponding master curve from nonisothermal data. It follows that nonisothermal DSC measurements provide the same crystallization kinetic information as isothermal DSC Measurements, only over a wider range of temperatures. The shift factors obtained from experimental data alone are compared in turn with the corresponding values calculated from the Avrami equation, the Hoffman-Lauritzen expression, and the Nakamura equation as a means of evaluating these models individually. It is concluded that the Avrami equation is very good at describing isothermal crystallization kinetics, the Hoffman-Lauritzen extrapolation of the limited isothermal data to a wide range of temperatures is quite good, and the Nakamura equation yields reliable crystallization kinetic information over a narrower range of temperatures than nonisothermal data alone without using any specific model.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 79
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 754-758 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The effect of hot curing of unsaturated polyester resin on the dynamic relaxation time was studied using dielectric measurements along with two dynamic mechanical measurement methods. It was found that the dynamic response during cure was a material frequency dependent property and did not depend on the measurement method. All relaxation times, measured during cure, by all three measurement methods used, converged to a single equation: τ(t)av=atb where t= curing time, a, b=constants. The increase of the relaxation time during cure followed the same trend as a friction factor, which was found to increase with conversion. The crosslinking density was found to increase slowly with conversion, while the relaxation time increased exponentially. These two different modes of behavior during cure explain the high resolution of dynamic measurements as a cure monitoring tool, which can easily detect small curing changes. This behavior of the relaxation time was explained by the sharp rise of activation energy due to a parallel decrease of free volume at high conversion.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 80
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995) 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 81
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 778-785 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: This paper investigates the effect of matrix ductility on toughness in a carboxyl-terminated butadiene-acryionitrile copolymer (CTBN) toughened diglycidyl ether of bisphenol-A (DGEBA)-piperidine system. Two kinds of epoxides were blended separately into this system to change the matrix ductility. One was a rigid and polyfunctional 4,4′-diaminodiphenol methane (MY720), and the other was a flexible diglycidyl ether of propylene glycol (DER732). The matrix Tg was significantly changed, but without alteration of the microstructure of the dispersed rubbery phase. The result of fracture energy tests reveals that the toughness of the neat epoxy resins increases slightly with the increase in the resin ductility. The toughness of the rubber-modified epoxy resins increases strongly with matrix ductility. Studies on the morphology of the toughened systems and their fracture surfaces indicate that the size of the plastic deformation zone under constant rubbery-phase morphology is determined by the multiple but localized plastic shear yielding. Increasing matrix ductility increases the size of the plastic deformation zone by inducing more extensive shear yielding. In addition, fracture surfaces reveal that as the matrix rigidity is increased, an increasing proportion of the fracture energy is dissipated by rubber cavitation during crack initiation.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 82
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 797-804 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Recently, a model was developed for the nonisothermal crystallization of normal alkanes with chain lengths between 30 and 50. The model was derived based on the fundamental equation of Ozawa for nonisothermal crystallization, the surface nucleation theory, and the growth rate theory for extended chain crystals. In this paper, the proposed model is modified and extended to the case of polymer crystallization. Experimental differential scanning calorimetry data for three isotactic polypropylene resins with different molecular weights are presented at five cooling rates from 2 to 40 K/min. Model predictions are in excellent agreement with the experimental data for the three polymers at low and high supercoolings.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
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  • 83
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 813-822 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The effect of rigid particles on the fracture mode of polymers that yield with necking was analyzed theoretically with a model of regularly arrayed spherical particles. The adhesion between a polymer and particles was assumed to be weak, and particles were assumed to debond from the polymer before necking. A linear decrease in engineering draw stress with an increase in the filler content was derived. An increase in filler content leads to a transition in deformation mechanism. The transition depends on the ability of the polymer to strain-harden. If the ability to strain-harden is insignificant and the engineering fracture stress (strenght) of the polymer is lower than its yield stress, the transition is from ductile to brittle fracture. If the ability to strain-harden is essential and the strength of the unfilled polymer is higher than its yield stress, the transition (ductile-to-ductile) is from neck propagation to uniform ductile yield. The critical filler contents were determined for both transitions from the properties of an unfilled polymer. The ductile-to-ductile transition without embrittlement is possible if the strength of the unfilled polymer is higher than its yield stress. Results for polymers filled by weakly bonded particles were compared with polymers filled by particles that debond after the yield stress.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 84
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 837-851 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Liquid composite molding (LCM) processes such as resin transfer molding (RTM) and structural reaction injection molding (SRIM) have been perceived as high potential processes for the near-net-shape manufacturing of composite parts. This paper addresses two major issues in LCM technology: fiber wetting and void formation during mold filling. Flow visualization experiments were carried out to develop a better understanding of the flow induced voids. The formation and elimination of voids were studied using several liquids and a unidirectional stitched fiberglass mat. Void formation was correlated to capillary number and liquid-fiber-air contact angle.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 85
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 957-967 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Adhesion between two substrates is a complex phenomenon which at present is still not well understood. The important existing adhesion models (electrical, diffusion, thermodynamic adsorption, chemical, etc.) are reviewed in order to try to explain their mechanisms. Thermodynamic adsorption is now believed to be one of the most importnat mechanisms by which adhesion is achieved. Difusion and wetting are kinetic means in attaining good adsorption of a polymer at the interface. In the case of this model (thermodynamic adsorption), the notion of surface energy is developed and the importance of this property in the understanding of adhesion phenomena is emphasized. The methods of determining the surface characteristics of low and high energy solids are presented. The role played by acid-base interactions in adhesion is also mentioned.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 86
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 989-999 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The reaction kinetics of radical chain copolymerization of t-butoxycarbonyl-oxystyrene (TBS) and sulfur dioxide have been studied using a reaction/sampling apparatus that permits accurate determination of the reaction mixture concentrations during polymerization. The results are compared with the styrene-sulfur dioxide copolymerization kinetics. The influence of temperature and reactant concentrations on the polymerization rate and copolymer composition are reported. With increasing reaction temperature, the amount of SO2 incorporated and the molecular weight fo the copolymer are found to decrease. For a constant TBS concentration in the reaction solutio, raising the SO2 concentration causes an increase of SO2 incorporation in the copolymer, up to a maximum SO2 content corresponding to a TBS:SO2 mole ratio of 2:1. However, for a constant SO2 concentration, the amount of TBS incorporated in the copolymer increases with decreasing TBS concentration in the reaction solution. The polymerization rate and copolymer molecular weight increase proportionally with monomer concentration as expected for a normal radical chain polymerization mechanism. Comparison of these findings with various kinetic models for styrene-SO2 copolymerization indicates good agreement with models proposed by Barb (1-3) and Walling (4); however, the data do not agree with the predictions of Matsuda et al. (5) The understanding of the kinetics and reaction mechanism provided in this study will aid in the manufacture of this lithographically important copolymer.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 87
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1011-1015 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: In this paper we investigate a new approach for the automated sorting of post-consumer plastic waste. We show that rapid and relible identification of polymers can eb achieved using a combination of fixed-filter near-infrared spectroscopy and neural network data analysis, and we demonstrate the effectiveness of the proposed method for sorting polyethylene terephthalate, high density polyethylene, and poly(vinyl chloride). Finally, we discuss a proposed compact, rugged instrument based on the new sorting method. Owing to the flexibility gained by incorporating neural networds in our system, thismethod can easily be extended to include additional polymers.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 88
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1037-1045 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The dispersion of titanium dioxide agglomerates within linear low density polyethylene (LLDPE) melts has been investigated by using a cone-and-plate device installed within a temperature controlled oven. Observation of fragment evolution indicates that erosion is the predominant mechanism of dispersion. The erosion rate of titanium dioxide agglomerates in LLDPE was consistenty with the results obtained in previous dispersion studies of titanium dioxide in polydimethyl siloxane (PDMS). The effect of agglomerate dispersion on the optical, tensile, and dynamic mechanical properties of compounds incorporating titanium dioxide was also investigated. Changes in compound properties were correlated with observed morphology changes of agglomerates in order to clarify the effect of dispersion.
    Zusätzliches Material: 15 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 89
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1022-1030 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A dynamic simulation method has been developed of the fracture process of a fiber in a flow field using the particle simulation method proposed i a previous paper. The fiber is modeled with bonded spheres as a fiber model. The flexibility of the fiber model is altered by changing three parameters of the stretching, bending, and twisting constants between adjacent spheres. The stress induced in each bond of the fiber model as a result of deformation is formulated using displacement of the bodn distanc, bond angle, and torsion angle fr each pair of spheres. After deformation, the fiber model fractures at the bond at which the stress surpasses the strength of the fiber. The motion of the fiber model in a flow field is determined by solving the translational and rotational motion equations for individual spheres under the hydrodynamic force and torque exerted on them. The correctness of the method and formulation was verified by comparing the simulated deflection curve of a cantilever beam (with a concentrated load at the end) with the theoretical curve. Good agreement was found in both the deflection and slope of the beam. The fracture process of a fiber after bending deformation in a two-dimensional siimple shear flow was simulated under assumptions of an infinitely dilute system, no hydrodynamic interaction, and a low Reynolds number of a particle. The calculated critical conditions of the flow field for fiber fracture were compared with Forgacs and Mason's theoretical ones. Simulated values of the fracture condition of the fluid shear stress related to the Young's modulus of a fiber agree with theoretical ones over an aspect ratio of 15.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 90
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995) 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 91
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1061-1065 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The choice of photoinitiators is partly governed by the requirement of a high curing speed. Many reactive monomers and efficient photoinitiators have been synthesized and are commercially available. However, improved photoinitiator systems, exhibiting increasingly faster curing speeds and/or increased photosensitivity, are increasingly required. The intrinsic reactivity in the exicited states determines te interest of a given photoinitiator with reference to its efficiency. However, other factors e.g. high molecular absorption coefficients and a broad spectral absorption range, synergistic effects, yellowing, extractability, and th effect on the long-term stability, must be considered as important. An attractive field of research and development is found in the role played by decisive parameters affecting the reactivity of a given structure, such as chemical substitution in well-chosen positions, the character of water solubility, acid release ability, and copolymerization potential. Laser spectroscopy proved a most convenient tool for the real time investigation of the excited state dynamics and the processes involved.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 92
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1069-1076 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Chain extended perfluoroether oligomers were found to be miscible with bisphenol epoxy resins at all concentrations. These were evaluated as modifiers for anhydride cured resin systems, taking advantage of the carboxylic acid functionality at the chain ends. By altering the mixing and curing procedure different two-phases morphologies could be obtained varying from fine co-continuous networks, which produced transparent castings, to opaque systems consisting of precipitated heterogeneous particles. While the Tg and flexural modulus were found to be slightly lower than the control cure resin, the addition of the fluoroligomer modifier produced large increases in flexural strength, ductility, and fracture toughness. Samples with an IPN type morphology were found to exhibit an increase in ductility after aging at 200°C for three weeks proportionally to the concentration of fluoroligomer used.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 93
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1098-1105 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Evaporation behavior of water/solvent blends was estimated using the universal functional activity coefficient, UNIFAC, method. The evaporation rate from a free surface of a waterborne coating, WBC, containing a co-solvent was experimentally determined. These results were used to estimate the evaporation rate from wet films of a WBC containing a variety of co-solvents with a range of initial thickness. Knowing the composition of the WBC during the drying process, the change in the viscosity and the surface tension was determined. The results strongly support the development of a surface tension gradient in the film. It is also suggested that a surface tension gradient would accelerate the leveling of the ribs if a proper co-solvent were employed.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 94
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1113-1116 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The miscibility window of the 50/50 w/w poly(styrene-co-4-vinylphenyl)-dimethylsilanol/poly(n-butyl methacrylate) (ST-VPDMS/PBMA) blends prepared from toluene was studied and determined to be in the VPDMS composition range of 4 to 18 mole% in the copolymers. The observed miscibility window was to be compared to the range of 9 to 34 mole% found for the blends prepared from methyl ethyl ketone which was capable of competing for hydrogen bonding. The fact that the observed miscibility windows are influenced by the choice of solvents illustrates that an equilibrium state of polymer mixing is not always attained in solvent casting films and that caution needs to be exercised in studying polymer miscibility when solvent cast films are used.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 95
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1117-1123 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Double yields, as well as other complex yielding behavior, that are observed during the tensile deformation of the polyethylenes have been studied in a systematic manner. The conditions under which such yielding is observed were established by studying a set of linear polyethylenes and well-characterized ethylene copolymers of narrow molecular weight and composition distributions. A wide range in crystallinity levels were developed and the rate of deformation and the deformation temperature were varied. These experimental results make clear why such complex yielding processes are not always observed. A qualitative explanation, based on the postulate of a partial melting-recrystallization process during deformation, is given that encompasses all of the experimental data.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 96
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1133-1136 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A statistical study of the strength of unmodified and modified uniaxially drawn polypropylene tapes was carried out. The results show that the curve representing the distribution of strength for unmodified tapes reveals seven discrete levels corresponding to microdefects in the form of microcrazes and submicrocrazes. On introduction of modifying additive, three discrete strength levels were observed, corresponding to submicrocrazes. The strength of the modified polypropylene tape increase approximately twice compared to the strength of the initial material. The polyfunctional effect of the additives as artificial nucleators and regulators of the structure leads to an increase of the degree of crystallinity which in turn restrains the submicrocrazes development into microcrazes. The method used could be applied for objective analysis of the tensile characteristics of polymeric materials.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 97
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1145-1154 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The physical aging characteristics of oriented poly(ethylene terephthalate) (PET), have been studied ad functions of storage time and temperature below the glass transition temperature (Tg) of PET. The free volume relaxation, associated with aging, has been characterized by the enthalpy at Tg, as measured by differential scanning calorimetry. The effects of the free volume relaxation on mechanical properties and the mode of failure have been investigated. It has been determined that a correlation exists between the enthalpy of relaxation and the ductile-to-brittle failure transition. Molecular orientation reduces significantly the enthalpy of relaxation, resulting in the disappearance of the ductile-to-brittle transition when highly oriented samples are aged over time. It has been established that a minimum amount of orientation is required to reduce or eliminate the effects of PET aging. Molecular orientation has also been found to reduce craze formation when oriented PET is exposed to a stress-cracking medium at constant stress.
    Zusätzliches Material: 18 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 98
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1155-1160 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: An experimental study of the effect of crystallinity on the light scattering of regenerated cellulose tubular films is reported. Several films were prepared by varying manufacturing conditions, so that thickness and surface roughness were maintained approximately constant and the degrees of crystallinity varied between 38 and 66%. The scattered radiation intensity, measured between 220 and 550 nm decreases with the increasing wavelength. It was demonstrated that for the polymeric films studied, there was excellent agreement between crystallinity and scattering radiation intensity for a given wavelength. It was found that for crystallinity values less than around 57%, scattered radiation intensity decreases with increasing crystallinity, the reverse of that for crystallinity values greater than that percentage.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 99
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: This paper reports on the tensile properties of microcellular foams of three different thermoplastics, since there have been several reports in the literature, but with indefinite conclusions so far, that microbubbles act in a manner similar to rubber particles in toughening thermoplastics. Polystyrene (PS), styreneacrylonitrile copolymer (SAN), and polycarbonate (PC), were selected based on their different intrinsic ductilities. The gas supersaturation technique was used to generate samples with microbubbles. The effect of the presence of microbubbles inside the polymer matrix was separated from the effects of the pressure and thermal history experienced by the samples. Nitrogen gas dissolved into PS, and to a lesser extent into SAN, caused and increase of the tensile toughness, but this increased decayed with time as nitrogen gas diffused out of the samples. Furthermore, microcellularly foamed PS samples showed some limited improvement in terms of tensile toughness after all the nitrogen gas diffused out. SAN and PC showed deterioration of the tensile toughness in the presence of microbubbles.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 100
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1184-1190 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The kinetics of water sorption by starch filled polyolefins has been investigated using blends of commercial starch masterbatch with low density polyethylene (LDPE), high density PE (HDPE), and copolymers of ethylene with methyl acrylate (EMA), ethyl (EEA), AND n-butyl acrylate (EBA). Transient state diffusion coefficients (D) of water in the blends were determined using Fickian analysis of the initial stages of the sorption isotherms. Measured D values were several orders of magnitude lower than values reported for either pure starch of LIDPE by various investigators. Resin effects on D were on the order DHDPE 〈 DLDPE ≪ DEBA 〈 DEEA 〈 DEMA. The resin effects diminished as the starch content increased. The lower magnitude of D in the blends relative to pure LDPE was attributed to the sorption of water by the dry starch particles, in a manner similar to dual-mode sorption in glassy polymers. Copolymer effects were consistent with reduction in crystallinity caused by the comonomers. The dependence of the diffusion coefficient on starch content was not described by mixing models of heterogeneous systems of percolation theory.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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