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  • Chemistry  (33)
  • Polymer and Materials Science  (15)
  • Astrophysics
  • DOCUMENTATION AND INFORMATION SCIENCE
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  • 1990-1994  (23)
  • 1985-1989  (16)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1817-1827 
    ISSN: 0887-624X
    Keywords: polymer blends ; hydrogen bonding ; miscibility ; phase behavior ; equilibrium constants ; hexafluoroisopropanol groups ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dimensionless equilibrium constants describing the self-association of the hexafluoro-2-alkyl-2-propanol group have been determined from infrared spectroscopic data. Corresponding values of these equilibrium constants for a fully modified polyisoprene containing the hexafluoroisopropanol group (PHFPI) were calculated by taking into account differences in the molar volume of the model and the specific repeat unit of the polymer. Equilibrium constants describing the inter-association of PHFPI with methacrylate, acrylate, and acetoxy type carbonyl groups were obtained from spectroscopic studies of miscible PHFPI blends with poly(n-butyl methacrylate), poly(methyl acrylate), and an ethylene-co-vinyl acetate copolymer containing 70 wt% vinyl acetate. The set of equilibrium constant values were then used to calculate theoretical miscibility windows for the complete range of PHFPI blends with poly(n-alkyl methacrylate)s and four copolymers, ethylene-co-methyl methacrylate, styrene-co-methyl acrylate, ethylene-co-methyl acrylate, and ethylene-co-vinyl acetate. Experimental infrared studies confirm the general validity of the predicted miscibility windows. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1189-1193 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2039-2056 
    ISSN: 0887-624X
    Keywords: blends ; hydrogen bonding ; miscibility ; phase behavior ; equilibrium constants ; fluoropolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Theoretical calculations of miscibility windows for binary polymer blends in which one component is an essentially alternating copolymer of tetrafluoroethylene and vinyl alcohol (FVOH) are reported. FVOH has an inherently low solubility parameter [≈ 6.2 (cal. cm-3)0.5] that is outside the range commonly encountered in miscible polymer blends and thus represents a stringent test of the predictive capabilities of an association model we have used in previous work. The application of this model requires that we determine dimensionless equilibrium constants describing the self-association of a model compound 3,4-pentafluorobutan-2-ol (PFB) at 25°C from infrared spectroscopic data. Analogous equilibrium constants for FVOH were scaled from those of PFB by taking into account differences in the molar volume of the model and the specific repeat of the copolymer (see M. M. Coleman, J. F. Graf, and P. C. Painter: Specific Interactions and the Miscibility of Polymer Blends, Technomic, Lancaster, PA, 1991). Equilibrium constants describing the inter-association of FVOH with ester type carbonyl groups were obtained from spectroscopic studies of miscible blends with poly(ethyl methacrylate). These equilibrium constant values were then used to calculate theoretical miscibility windows for the complete range of blends of FVOH with polymethacrylates, ethylene-co-methyl acrylate, styrene-co-methyl acrylate, and ethylene-co-vinyl acetate copolymers. Experimental results performed in our laboratories confirm the general validity of the predicted miscibility windows. © 1993 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 28 (1986), S. 1241-1249 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Acoustic resonance densitometry (ARD) is reported as a method suitable not only for precise investigations into changes of specific gravity in bioreactor media but also as a technique able to provide an accurate wide range and direct determination of cellular mass in fermentation processes. It is further shown that this method can replace present optical procedures, minimizing dilution errors and operator involvement and is suitable for development as an on-line biomass monitoring system.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 33 (1989), S. 1379-1384 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Acoustic resonance densitometry (ARD) provides a highly reproducible and stable method for on-line measurement of culture biomass density. The technique provides a direct determination of changes in relative density of culture medium and cell mass. At cell concentrations higher than 106 cells mL-1this method can replace cell counts and provide a continuous measure of total cell mass. In cultures of hybridomas or U937 human lymphoma cells, the ARD value correlates well with cell number except when the average cell size changes during culture. It is argued that cell mass determined by ARD rather than cell number should be used as the basis for measurements of specific biological activity.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 994-1002 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Interpenetrating polymer networks (IPNs) of poly(ethylene oxide) (PEO) and a polyether substituted polysiloxane were synthesized containing variations of PEO content (35 and 65% dry network weight) and PEO systematically varied from low to high molecular weight (2,000, 8,000, and 20,000). Biocompatibility was assessed by measureing 111In platelet deposition in a baboon femoral ex vivo shunt. Mass transfer analysis revealed that platelet transport to PEO/polysiloxane surfaces was kinetically limited and correlated with both PEO content and molecular weight. Differences in material performance were noted particularly after the initial 30 min blood contact period. In mid and high PEO molecular weight networks (8,000 and 20,000), reduced platelet deposition was noted with increased PEO content. In materials of high PEO content (65%), mid and high PEO molecular weight samples had significantly lower levels of platelet adsorption than PDMS (60 min; p〈 0.05) or networks of low PEO molecular weight, coded 2K-65 (30 and 60 min; p 〈 0.05). The lowest level of platelet deposition was noted on 20K-65 networks, less than one platelet per 1,000 μm2.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 8 (1985), S. 112-118 
    ISSN: 0935-6304
    Keywords: Gas chromatography, GC ; Fused silica capillary columns ; Packed absorption columns ; Thick liquid phase films ; Natural, refinery, and reactor gas analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A gas chromatographic system consisting of one multiport valve, two (hot-wire and flame-ionization) detectors and two analytical columns (one thick-film capillary and one packed adsorption column) is used for the analysis of gas samples containing a number of inorganic compounds (hydrogen, argon, oxygen, nitrogen, carbon monoxide, and carbon dioxide) and organic compounds. Examples include samples containing hydrocarbons up to n-nonane and benzene and toluene. The system also permits the analysis of more complicated samples containing, for example, alcohols, in addition to hydrocarbons.
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 4 (1992), S. 316-322 
    ISSN: 0899-0042
    Keywords: chiral LC ; drug enantiomers ; modelling ; central composite desire ; optimization ; β-cyclodextrin ; response surface ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The application of a central composite design to the enantiomeric separation of the antifungal drug tioconazole is investigated. The design involves application of a mathematical model to the data to model the response in regions of the factor space not investigated in the experimental design. The significance of the variable terms in the model is assessed statistically and those terms declared not significant are removed from the model. The statistical adequacy of these reduced models is discussed, together with an examination of the prediction errors of the models. Three-dimensional predicted response surfaces for the complete models are presented and the predictive performance assessed. © 1992 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 857-860 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polymer blends of an amorphous polyamide with poly(2vinyl pyridine) (P2VP) are presented. Differential scanning calorimetry results suggest that the system exists as a single phase material as evidenced by a single glass transition temperature. However, as illustrated by light scattering studies, this miscible binary mixture possesses a relatively low, lower critical solution temperature (LCST). Fourier transform infrared (FTIR) spectroscopic investigations indicate that the interactions occur in the blend between the N—H group of the polyamide and the —N: atom of P2VP and that the strength of the Interactions between the components is nearly identical to that occurring in the self-association of the pure amorphous polyamide. Additionally, by monitoring the concentration of “free” carbonyl groups, a quantitative measure of the number of interactions occurring in the blend is obtained.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1801-1822 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this, the first paper in a series on neck formation and steady-state drawing of polymeric fibers and films under uniaxial tension, the emphasis is laid on those aspects of the mechanics of cold drawing that are not sensitive to viscoelastic effects and, therefore, can be treated by use of constitutive assumptions appropriate to elastic materials. It is here shown that a unidimensional theory which has been employed to model the mechanics of slender bars in tension6 can be derived as an approximation for three-dimensional bars and, in a sense which can be made precise, is valid to within an error of the order of the fourth power of the thickness. A particular constitutive equation for incompressible, three-dimensional, elastic materials is explored in detail and is found to yield, for such slender bars as thin fibers and wide (but thin) strips of film, equations of equilibrium whose solutions are in good qualitative accordance with the necks and drawing configurations observed in practice.
    Additional Material: 7 Ill.
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