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  • Chemical Engineering  (118)
  • Physics  (46)
  • Atomic, Molecular and Optical Physics  (28)
  • Wiley-Blackwell  (192)
  • National Academy of Sciences
  • 1995-1999  (192)
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  • Wiley-Blackwell  (192)
  • National Academy of Sciences
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1261-1271 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This study clarifies and quantifies factors which increase the ductility of a low-molecular-weight propylene homopolymer having an intrinsic viscosity of 0.89 dl/g. The tensile behavior of homopolymer/ethylene-propylene rubber (EPR) blends was studied from the viewpoint of the associated molecular structure of EPR and its compatibility with the homopolymer. When EPR is “dissolved” in a homopolymer, the glass transition temperature (Tg) of the amorphous phase of a homopolymer was found to shift to a lower temperature, with homopolymer/EPR compatibility being subsequently evaluated using this shift, i.e., Δtg. Results show two conditions are required to improve the ductility of the low-molecular weight propylene homopolymer: ΔTg must be ≥ 3°C and ≥ 30 wt% EPR must be blended with the homopolymer.
    Additional Material: 18 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2597-2605 
    ISSN: 0887-6266
    Keywords: positron annihilation ; open space ; relaxation ; subsurface ; polyethylene ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Open spaces in the subsurface region (〈10 μm) of very low density polyethylene were probed by a monoenergetic positron beam. From measurements of Doppler broadening spectra measurements of the annihilation radiation and the lifetime spectra of positrons as a function of incident positron energy, the size of the open spaces in the region of 0-3 μm was found to be larger than that in the deeper region. This was attributed to the cooperative motion of large segments of molecules which is activated near the surface. After the freezing in of such motions (below 230 K), although the lineshape parameter S in the bulk was almost constant, S in the region of 0-3 μm decreased with decreasing temperature. This discrepancy was associated with the presence of the open spaces with an excess content and the resultant contraction of amorphous structure near the surface. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2597-2605, 1998
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 43 (1997), S. 1091-1099 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Two reversible reactions are involved in YBa2Cu3O6+x formation: a reaction between BaCO3 and CuO forming BaCuO2 and CO2, and a reaction of BaCuO2 with Y2O3 and CuO forming YBa2Cu3O6 which undergoes phase transformation to YBa2Cu3O6+x upon cooling. In-situ isothermal time resolved HT-XRD of a thin film was used to quantify the effect of CO2 on the kinetics of the first reaction. Increased CO2 partial pressure shifts the reactions to higher temperatures. At high CO2 partial pressure (〉2 vol. %), the rate of the first reaction becomes essentially a step process with a very high activation energy. Noninstantaneous nucleation of the reaction products occurs at low CO2 partial pressure (0.5-1%) and temperatures (700°C). The data fit a 2-D diffusion-controlled mechanism with a zero nucleation rate for BaCO3 decomposition and a second-order nucleation rate for YBa2Cu3O6 formation. A comparison of the kinetics of a thin film (10 mm) as determined by HT-XRD with those of a thick sample (2 mm) determined by TG revealed that the transport of CO2 within the sample pores and to the ambient gas significantly affect the decomposition of BaCO3. For example, the formation of YBa2Cu3O6 in a thick precursor layer occurs in the 840 to 940°C range, exceeding by about 200°C that in which it is formed in thin films.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 42 (1996), S. 301-318 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Experiments conducted quantify the macroscopic hydrodynamic characteristics of various scale 2-D bubble columns, which include dispersed and coalesced bubble regimes characterized by two flow conditions (4- and 3-region flow) with coherent flow structures. Hydrodynamic behavior is analyzed based on flow visualization and a particle image velocimetry (PIV) system. Columns operated in the 4-region flow condition comprise descending, vortical, fast bubble and central plume regions. The fast bubble flow region moves in a wavelike manner, and thus the flow in the vicinity of this region is characterized macroscopically in terms of wave properties. In columns greater than 20 cm in width, the transition from the dispersed bubble flow regime to the 4- and then to 3-region flow in the coalesced bubble regime occurs progressively with gas velocities at 1 and 3 cm/s, respectively. The demarcation of flow regimes is directly related to measurable coherent flow structures. The instantaneous and time-averaged liquid velocity and holdup profiles provided by the PIV system are presented in light of the macroscopic flow structure in various 2-D bubble columns. Numerical simulations demonstrate that the volume of fluid method can provide the time-dependent behavior of dispersed bubbling flows and account for the coupling effects of pressure field and the liquid velocity on the bubble motion. Comparison of computational results with PIV results for two different bubble injector arrangements is satisfactory.
    Additional Material: 27 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 43 (1997), S. 3260-3263 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 604-618 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The present study develops a numerical simulation program to predict the transient behavior of fiber orientations together with a mold filling simulation for short-fiber-reinforced thermoplastics in arbitrary three-dimensional injection mold cavities. The Dinh-Armstrong model including an additional stress due to the existence of fibers is incorporated into the Hele-Shaw equation to result in a new pressure equation governing the filling process. The mold filling simulation is performed by solving the new pressure equation and energy equation via a finite element/finite difference method as well as evolution equations for the second-order orientation tensor via the fourth-order Runge-Kutta method. The fiber orientation tensor is determined at every layer of each element across the thickness of molded parts with appropriate tensor transformations for arbitrary three-dimensional cavity space.
    Additional Material: 19 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 281-288 
    ISSN: 0887-6266
    Keywords: side-chain liquid-crystalline polymer membrane ; pervaporation ; benzene/cyclohexane mixture ; state-transformation ; benzene permselectivity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When a benzene/cyclohexane mixture of 10 wt % benzene was permeated through side-chain liquid-crystalline polymer (LCP) membranes by pervaporation at various temperatures, the permeation rate increased with increasing permeation temperature. The LCP membranes also exhibited a benzene permselectivity. The permselectivity for the benzene/cyclohexane mixture through the LCP membrane was different in the glassy, liquid-crystalline, and isotropic states. The LCP membrane had different apparent activation energies for permeation at each state. LCP membrane in the liquid-crystalline state had the highest apparent activation energy of the three states. Results suggest that the benzene permselectivity was influenced by changes in the LCP membrane structure, i.e., a state-transformation. It was found that a balance of the orientation of mesogenic groups and the flexibility of the siloxane chains was very important for benzene permselectivity. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 281-288, 1998
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1857-1872 
    ISSN: 0887-6266
    Keywords: hybrid polymers ; rheology ; reptation ; silsesquioxane polymers ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We report on the viscoelastic behavior of linear thermoplastic nonpolar hybrid inorganic-organic polymers. These materials have been synthesized through copolymerization of an oligomeric inorganic macromer with 4-methylstyrene where the inorganic portion of the material is a well-defined polyhedral oligosilsesquioxane (POSS), R7(Si8O12)(CH2CH2C6H4C=CH2), with R = c-C6H11 or c-C5H9. A series of 4-methyl styrene copolymers with approximately 4, 8, and 16 mol % POSS macromer incorporation were investigated. Rheological measurements show that the polymer dynamics are profoundly affected as the percent of POSS increases. In particular, a high-temperature rubbery plateau develops (where a terminal zone is not observed), despite the fact that the parent poly 4-methylstyrene is unentangled. It is also observed that the thermal properties are influenced as the percent of POSS incorporation increases, with increases in the glass and decomposition temperatures. The results suggest that interchain interactions between the massive inorganic groups are responsible for the retardation of polymer chain motion, a mechanism similar to the “sticky reptation” model conceived for hydrogen-bonded elastomers and developed by Leibler et al. [Macromolecules, 24, 4701 (1991)]. Control over the interchain interactions would also give rise to the observed increases in glass transition and the establishment of a rubbery plateau. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1857-1872, 1998
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1601-1609 
    ISSN: 0887-6266
    Keywords: positron annihilation ; polyethylene ; polypropylene ; polystyrene ; glass transition ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transition and relaxation processes of polyethylene (PE), polypropylene (PP), and polystyrene (PS) were studied by the positron annihilation technique. From measurements of lifetime spectra of positrons as a function of temperature, the lifetime of ortho-positronium, τ3, and its intensity, I3, were found to increase above 260 K for PP. This fact was attributed to a cooperative motion of large segments of molecules above the glass transition temperature, Tg. For PE, above Tg (140 K), the value of τ3 increased, but the temperature coefficient of I3 was negative below 230 K. From this fact, for PE, the molecular motions that cause the glass transition were associated with a rearrangement of molecules by local motions such as kink motions. The discrepancy between the results for PE and PP was attributed to the presence of methyl groups in PP and the resultant suppression of the local motions. For PS (Tg = 340 K), the molecular motions were found to start above 260 K, but those were suppressed by an interphenyl correlation. Detailed annihilation characteristics of positrons in polymers were also discussed. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1601-1609, 1997
    Additional Material: 12 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 699-707 
    ISSN: 0887-6266
    Keywords: side-chain liquid-crystalline polymer ; pervaporation ; benzene/cyclohexane mixtures ; state transformation ; permselectivity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The side-chain liquid-crystalline polymer (LCP) was synthesized by the addition of the mesogenic monomer to poly(methylsiloxane) with Pt catalyst. When the benzene/cyclohexane mixtures were permeated through the LCP membranes by pervaporation at various temperatures, the permeation rate increased with increasing benzene concentration in the feed solution and permeation temperature. Though the LCP membranes exhibited a benzene permselectivity, a mechanism of the permeation and separation for the benzene/cyclohexane mixtures was different in the glassy, liquid-crystalline and isotropic state of the LCP membranes. These results suggested that the permselectivity was fairly influenced by the change of the LCP membrane structure, that is, a state transformation. It was found that a balance of the orientation of mesogenic groups and flexibility of siloxane chains is very important for the permeability and selectivity. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 699-707, 1997
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