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  • Chemical Engineering  (9)
  • Analytical Chemistry and Spectroscopy  (5)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 7 (1993), S. 360-362 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The production of carbon clusters (but not fullerenes) from coal-derived material by the use of laser desorption mass spectrometry is described. Benzo(e)pyrene, a standard polynuclear hydrocarbon found in coal tars, also gave carbon clusters despite using low laser power to avoid pyrolysis of target molecules. Positive- and negative-ion spectra of the standard included carbon clusters. These clusters are formed by the laser energy and can be confused with aromatic hydrocarbons of the same nominal masses. They have no relevance for studies of coal structure.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The use of a laser-desorption mass spectrometer to examine a coal liquefaction extract known to contain high-molecular-mass material (from size-exclusion chromatography) has shown the presence of components of molecular mass in excess of 104Da for the first time. The molecules detected differ from each other in molecular mass by a few hundred or a few thousand Da. These preliminary results indicate that the basic coal-structure molecules probably consist of aromatic clusters on a chin, in reasonable agreement with current theories of coal structure.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Molecular masses up to 270 000 u have been observed during matrix-assisted laser desorption mass spectroscopy on a sample of bituminous coal; the major fraction of desorbed ions appeared between m/z values of 800 and 5000. Similar mass distributions have been found in a coal-liquefaction extract and a pyrolysis tar. The highest molecular masses identified in this work far exceed previously reported high molecular masses found in coal-derived products (12 000 u), which were also detected by laser-desorption mass spectrometry.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 21 (1981), S. 285-293 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Measurements to obtain the dynamic moduli G′(ω) and G″(ω) for several polymer liquids were made with the Rheometrics mechanical spectrometer using the eccentric rotating disk (ERD) and the forced oscillation methods. The ERD data were corrected for instrument compliance with the Macosko-Davis formula. Oscillatory results were confirmed in several separate studies including testing of a Newtonian liquid and an elastic solid. Agreement between the two geometries on G′(ω) and G″(ω) was generally good (±5 percent) for |G*| less than 2 × 106 dyne/cm2. If no compliance correction was applied, departures occurred near a |G*| an order of magnitude lower, indicating strongly the need for applying a compliance correction to ERD data for most polymer systems. However, as |G*| approached 107 dyne/cm2 (where compliance corrections of 50 percent or greater occurred), the two geometries yielded results which differed by 20 percent or more. No single variable was found which correlated the departures for different liquids. Nevertheless, the departures were such that values obtained in the two geometries for the plateau modulus of polyethylene, GN0 ≈ 2 × 107 dyne/cm2, agreed within about 10 percent.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 20 (1980), S. 432-440 
    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: Welded joints were made under a range of conditions in polypropylene, glass fiber reinforced polypropylene and poly (methylmethacrylate) bars. Melt flow in the weld was investigated by microscopy and by contact microradiography, and weld strengths were measured by tensile tests. The fracture toughness of the weld zone was determined by tests on double edge notched specimens. The study shows that weld strength is strongly affected by hot plate temperature, heating time and melt flow during welding. Insufficient heating or melt flow results in incomplete bonding. Excessive melt flow produces strong transverse orientation. Both reduce strength, but in different ways, which can be distinguished by fracture mechanics tests.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 33 (1993), S. 303-310 
    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: Pipes of isotactic polybutene-1 (PB) have been exposed to internal water and external air in pressure tests at 105°C. The pipes exposed to different internal pressures exhibited different failure mechanisms, referred to as stages I, II, and III. Samples taken from these pipes have been analyzed by infrared (IR) spectroscopy, wide-angle X-ray scattering (WAXS), size exclusion chromatography (SEC), and differential scanning calorimetry (DSC). IR spectroscopy and WAXS confirmed that thermal oxidation of the amorphous part of the polymer accompanied the onset of stage III. Thermal oxidation led to extensive molar mass reduction and to a significant increase in mass crystallinity and melting peak temperature. Extensive and visible degradation in pipes failing according to stage III was confined to so-called “oxidation spots.” The latter were first formed at the outer wall and propagated inwards, finally constituting approximately 50% of the wall thickness. The antioxidant concentration profiles obtained by DSC were always symmetrical and were successfully adapted to a previously developed model. It was shown that migration of the antioxidant was the dominant loss mechanism, that the diffusion coefficient was constant through the pipe wall, and that the evaporative loss to the external air was marginally greater than the loss to the internal water phase. Chemical consumption of the antioxidant was found to be negligible.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 649-657 
    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: Changes in polymer structure and antioxidant concentration have been systematically studied as functions of temperature, hoop stress, exposure time, and location in pipe wall on pressure tested pipes of medium density polyethylene. The pressure tests have been performed with water as the internal medium and air as the external medium at temperatures in the range 80 to 105°. Infrared spectroscopy shows that oxidation is initiated at the inner wall surface just prior to the onset of the so-called stage III fracture. X-ray diffraction and size exclusion chromatography show that oxidation involves only the amorphous phase and results in a significant molar mass reduction. The near-inner-wall material exhibits a 10% reduction in mass average molar mass before the onset of stage III fracture and thereafter a more dramatic decrease. Oxidation induction time measurements by differential scanning calorimetry show that the antioxidant concentration is almost twice as high in the center of the wall as in the near-inner-wall and outer-wall material of the unexposed pipe, that the loss of antioxidant is anomalously rapid at the beginning of the high temperature exposure, and that the antioxidant concentration profile gradually becomes more skewed towards the outer wall on prolonged exposure. The data presented in this paper are used in a parallel paper for modeling purposes.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 658-667 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper is the first in a series of related papers describing the application of a diffusion/reaction model to the loss of antioxidants from polyolefins in hot-water applications. The model, which is derived in detail, describes the time evolution of antioxidant concentration profiles in the exposed material in terms of adjustable parameters. The parameters describe the rates of diffusion, evaporation, extraction, and chemical reaction of antioxidant. Parameter values are determined by least-squares fitting of the calculated concentration profiles to experimental profiles. The model is applied to a commercial medium density polyethylene pipe material, where antioxidant concentration data from thermal analysis is available for water/air (internal/external) exposure at three temperatures. A comparison of parameter values with literature data is undertaken. The temperature dependence of the parameters is considered and activation energies are compared with literature values. The relative importances of the loss mechanisms are discussed. The effect of boundary conditions on parameter values is considered by application of the model to a limited amount of available data for air/air and water/water exposures. The results indicate that for water/air exposure, extraction by the water phase is the dominating loss mechanism.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The two-scale turbulence concept is recommended for modeling the turbulence in a baffled vessel equipped with a Rushton-type turbine impeller. A three-equation isotropic turbulence model is proposed that employs the balance equations for: the kinetic energy of the large scale vortices; the kinetic energy of the inertial subrange eddies; and the dissipation rate of the small-scale turbulence. The energy transfer rate from the large-scale vortices is prescribed algebraically. Flow patterns are modeled by solving the transport equations for vorticity, stream function, and tangential momentum. The Reynolds stresses are modeled by means of the effective viscosity, based on the three-equation model of turbulence. The calculated profiles of the mean velocity at the tank wall agree with experimental data obtained in the same system by means of a Pitot tube.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A study has been made of the individual film coefficients of mass transfer for two binary liquid-liquid systems of differing physical properties, namely methyl isobutyl carbinol-water and methylethyl ketone-water, in a 4-in. diam. extraction column operated as a spray column and with 1/2-in. Raschig ring packing. The value of Ht for the dispersed phase was found to be a constant, C1 for a given system in a given column. The Ht values for the continuous phase could be correlated by the equation, \documentclass{article}\pagestyle{empty}\begin{document}$$(H_t )_c = C_2 (V_c /V_d )^n $$\end{document} Values of the constants C1, C2, and n are tabulated along with the values found by earlier investigators for other systems and column packings. The Ht values have been reduced to area base coefficients by the expression for droplet surface area proposed by Gaylor and Pratt (3).Presaturation of either phase was found to have no effect on mass transfer rates. There appears to be relatively little difference in the efficiency of spray and packed columns for systems of low interfacial tension, but for high interfacial-tension systems packed columns are considerably more efficient than spray columns.While no definitive correlations for the effect of physical properties are proposed, there are some indications that n is a function of the viscosity ratio of the two liquid phases and that C2 is a function of the 1/4 power of the groups (dΔργ/μ2c)(μc/μa) and (NS c)c. No correlation was found for the effect of physical properties on (Ht)d.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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