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  • Polymer and Materials Science  (37)
  • Analytical Chemistry and Spectroscopy  (17)
  • Chemical Engineering  (13)
  • Capillary electrophoresis  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Configurational entropy of polyethylene and other linear polymers (1966)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 869-880 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The configurational entropy of the polyethylene chain at the melting points calculated in two ways. In both calculations, tetrahedral angles and discrete trans and gauche arrangements of all bonds are assumed, and trans bonds are assumed more stable than gauche by energy U1. First, calculations are made on chains of up to N = 18 bonds, disallowing all configurations having overlapping atoms, and the result is extrapolated to large N. Second, a calculation is made directly for long chains, with overlaps excluded only over every short chain segment. The results are in almost exact agreement, suggesting that the second method can be safely used with other molecules. The calculated configurational entropy is in line with that suggested by the entropy of fusion, assuming the chains to acquire a configurational freedom in the melt which approaches that of independent chains.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1966.160040604
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  • 2
    Electronic Resource
    Electronic Resource
    Equation of state and the thermodynamic properties of liquid polymers: Application of the Hirai-Eyring modelPresented at Symposium on Thermodynamic Properties of Bulk Polymers, National Bureau of Standards, Gaithersburg, Md., March 10-12, 1969. (1970)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1337-1360 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the Hirai-Eyring model for the liquid state is capable of accurately describing the p, V, T behavior of liquid polymers in the temperature range over which measurements are now made, and below. Once the parameter choices necessary to accomplish the fit are made for a particular polymer, the excess thermodynamic functions (differences in properties, liquid less solid) are determined by the same parameters. Above the glass transition temperature Tg the volume, excess enthalpy, and square of the excess entropy are predicted by the model to be essentially linear with temperature, in agreement with experiment. Below Tg, these functions do not remain linear (as is usually assumed in extrapolating the equilibrium behavior to low temperatures), but instead they rapidly approach zero in a continuous way as the temperature is lowered. These remarks apply to glass-forming materials composed of small molecules, as well as to polymers. The “paradox” raised by Kauzmann is thus resolved, and the Gibbs-DiMarzio second-order transition appears to be unnecessary.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1970.160080807
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  • 3
    Electronic Resource
    Electronic Resource
    Viscoelastic properties of branched polyethylene melts (1970)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 455-465 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical properties of branched polyethylenes in the molten state were determined in the frequency range 10-3-10 radians/sec. The materials tested have remarkably similar rheological properties even though they vary greatly in molecular weight and molecular weight distribution. The similarity in properties is attributed to the influence of long chain branching on the relaxation spectra. A mechanistic argument is proposed to relate the observed behavior to molecular entanglement coupling. The concept of entanglement coupling involving long-chain branching leads to the expectation that the quasi-Newtonian and non-Newtonian viscosities of branched polymers may be either greater or less than those of linear polymers of the same species, which have comparable molecular weights. This is borne out by experiment.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1970.160080311
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  • 4
    Electronic Resource
    Electronic Resource
    Dielectric properties of an epoxy resin and its composite I. Moisture effects on dipole relaxation (1986)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 1771-1784 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Dipole relaxation dielectric loss behavior of a fiberglass-epoxy composite has been studied as a function of moisture uptake. A single widely distributed loss peak, centered at -16°C for 10 kHz measurement, is observed in the dry composite. Very low moisture concentrations (〈0.1%) interact with the composite, through either dipole pairing or by inducing chemical changes, to decrease loss intensity. At moisture concentrations from 0.1 to 1.4%, loss peak intensity generally increases with moisture uptake. Over this moisture concentration range water dipoles presumably relax in phase with the epoxy segments or side groups upon which they adsorb. Arrhenius relaxation activation energy decreases, and improved loss peak definition at increasing moisture concentrations is interpreted as indicating resin plasticization by adsorbed moisture. At moisture concentrations above 1.4%, the appearance of a second loss peak suggests formation of a new colloidal or weakly adsorbed moisture phase, as well as the saturation of primary adsorption sites.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1986.070310622
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  • 5
    Electronic Resource
    Electronic Resource
    Capillary gas chromatography/mass spectrometry of cholesteryl esters with negative ammonia chemical ionization (1987)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1987), S. 131-140 
    Details
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mixtures of both synthetic and naturally occurring (human plasma) cholesteryl esters have been examined by capillary gas chromatography/mass spectrometry (GC/MS). A magnetic sector mass spectrometer was used and a variety of ionization modes were assessed with a view to obtaining structural information on intact cholesteryl esters. By employing ammonia as reagent gas, with negative ion scanning, spectra were produced from which the nature of steryl and fatty acyl moieties could be readily deduced. Analyses were performed at an ion source temperature of 300°C in order to maintain the integrity of the gas chromatographic profile. The technique described is of general use for the GC/MS analysis of steryl esters, particularly in conjunction with magnetic sector instruments.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200140307
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    Paper (German National Licenses)
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  • 6
    Electronic Resource
    Electronic Resource
    Physics of polymer surfaces and interfaces. Edited by Isaac C. Sanchez, Butterworth-Heinemann, 1992, 336 pp. (1994)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 1088-1089 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690400623
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  • 7
    Electronic Resource
    Electronic Resource
    Mass transfer in liquid-lithium systems (1960)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 6 (1960), S. 139-144 
    Details
    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 behavior of type-304 stainless steel in a forced-convection closed-loop lithium system was investigated over a wide range of temperatures and velocities. Fundamental information concerning the mechanism for mass transport has been obtained by examining solution and deposition effects along flat plates. The rate-determining process for solution is transport from the solid to the interface, whereas deposition rates are liquid-phase controlled.Liquid-phase mass transfer coefficients were correlated with a maximum deviation of approximately 15% by the use of von Kàrmàn's analysis of the turbulent boundary layer along a flat plate, combined with the Chilton-Colburn empirical modification of the Schmidt group. In contrast no adequate model is available for the prediction of solution rate constants which must be determined experimentally. Mean values of the solution rate constants ranged from 0.154 to 0.750 × 10-5 cm./sec. at temperatures from 510° to 612°C. These values are on the order of 103 smaller than corresponding liquid-phase mass transfer coefficients.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690060127
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  • 8
    Electronic Resource
    Electronic Resource
    Mass transfer with liquid lithium in circular conduits (1961)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 7 (1961), S. 216-220 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Forced convection mass transfer between circular tubes and liquid lithium was experimentally investigated over a range of Schmidt numbers from 40 to 57 and Reynolds numbers from 5,550 to 22,500. Information concerning the mechanism for mass transfer was obtained by measuring local solution and deposition rates as a function of distance along the tubes. Observed entrance effects for the solution process suggest that it involves the parallel mechanisms of diffusion through a solid film and through occluded liquid in grain boundaries. It is indicated that the relative contributions of these processes changes with increasing temperature.A j-factor correlation of existing liquid metal mass transfer data for fully developed conditions in circular conduits is presented and indicates that an exponent of 0.112 for NRe best represents the data. This result agrees well with other studies (9).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690070210
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  • 9
    Electronic Resource
    Electronic Resource
    The rate of glycerol absorption by ion exchange resins (1963)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 283-287 
    Details
    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: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690090229
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  • 10
    Electronic Resource
    Electronic Resource
    Toughening of unsaturated polyester and vinyl ester resins with liquid rubbers (1995)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 35 (1995), S. 1086-1097 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A comprehensive study of toughening unsaturated polyster and vinyl ester resins by addition of liquid rubbers was carried out by considering the effects of cure temperature and gel time on final resin/rubber morphology. The objective was to produce a dispersed rubber phase consisting of particles less than 15 μm in diameter with the addition of limited amounts of rubber, so as not to seriously reduce the modulus and strength of the base resin. A variety of liquid rubbers was used including those based on poly(butadiene acrylonitrile), poly(epichlorohydrin), and two poly(acrylates). Fracture toughness of unmodified and rubber modified materials was measured using the compact tension (CT) test geometry. Significant improvements in fracture toughness were achieved with little to no change in Young's modulus or glass transition temperature. With modest rubber additions, the fracture toughness increased up to 62% for the polyester resin and up to 116% for the vinyl ester resin. In general, fracture toughness increases with increases in volume fraction of rubbery second-phase particles. However, results suggest that two-phase particles may be more effective tougheners than single-phase particles. The toughening mechanism appears to depend on the type of rubbery particle morphology present.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760351304
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