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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 17 (1984), S. 1718-1723 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Numerische Mathematik 21 (1973), S. 345-349 
    ISSN: 0945-3245
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Summary TheL 2 error in the “nearly zero” quadratic approximate solution to Poisson's equation is shown to be of optimal order. The same method of proof can be used to show that theL 2 error with a space of cubics developed by Ridgway Scott is optimal.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 528-538 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A variety of amphiphilic molecules reversibly and spontaneously self-assemble in aqueous solution forming a polydisperse population of asymmetric aggregates. In binary water/surfactant systems, aggregates may be either oblate or prolate and form corresponding orientationally ordered phases. Such binary systems are modeled using a lattice statistics calculation of the configurational entropy of a polydisperse collection of hard rods and plates, combined with a phenomenological description of aggregate assembly. Using parameter values relevant to micellar surfactant systems, a series of phase diagrams and associated particle size distributions have been computed. Depending upon the competition between rod and plate growth, the concentration dependent transition sequences I→A, I→P, and I→A→P (where I≡isotropic micellar, A≡axial nematic, and P≡planar nematic) are seen. The A→P transition occurs when rod and plate growth are equally favorable and is discussed in detail. Qualitative comparisons are drawn between the calculated phase behavior and experimental results. No stable biaxial nematic phases are predicted for binary systems in the absence of positional order.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 7915-7930 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An approach to the investigation of molecular structures in disordered solids, using two-dimensional (2D) nuclear magnetic resonance (NMR) exchange spectroscopy with magic angle spinning (MAS), is described. This approach permits the determination of the relative orientation of two isotopically labeled chemical groups within a molecule in an unoriented sample, thus placing strong constraints on the molecular conformation. Structural information is contained in the amplitudes of crosspeaks in rotor-synchronized 2D MAS exchange spectra that connect spinning sideband lines of the two labeled sites. The theory for calculating the amplitudes of spinning sideband crosspeaks in 2D MAS exchange spectra, in the limit of complete magnetization exchange between the labeled sites, is presented in detail. A new technique that enhances the sensitivity of 2D MAS exchange spectra to molecular structure, called orientationally weighted 2D MAS exchange spectroscopy, is introduced. Symmetry principles that underlie the construction of pulse sequences for orientationally weighted 2D MAS exchange spectroscopy are explained. Experimental demonstrations of the utility of 2D MAS exchange spectroscopy in structural investigations of peptide and protein backbone conformations are carried out on a model 13C-labeled tripeptide, L-alanylglycylglycine. The dihedral angles φ and ψ that characterize the peptide backbone conformation at Gly-2 are obtained accurately from the orientationally weighted and unweighted 2D 13C NMR exchange spectra. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 2603-2616 
    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: Scaling parameters for two PVT equations of state are evaluated for 11 polymer melt systems using a nonlinear least square fitting algorithm that analyzes all of the experimental data simultaneously. Two different criteria are considered in this evaluation. In the first method, the fitting criterion is the difference between the calculated and experimental volume. In the second method, the criterion is the difference between the calculated and experimental pressure. In both cases, the differences between the scaling parameters obtained using the simultaneous fit procedure and those obtained using the earlier consecutive fit procedure are a few percent, which can have a significant effect in some calculations. In addition to being a more consistent method of evaluating scaling parameters, the simultaneous fit procedure leads to much better agreement between calculated and experimental values, in some cases by a factor of 2.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 983-991 
    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: An algorithm is discussed for determining best-fit scaling parameters in the PVT equation of state of polymer melts from experimental data. The underlying theoretical expressions are those employed in our preceding work. There it was assumed that values of pressure and temperature are known exactly and experimental uncertainty was admitted in the volume solely. This condition is now relaxed to allow for errors in P and T also. The methodology developed involves multiple small nonlinear fitting problems for two or three unknowns at a time. We employ it on the experimental data base in the earlier work, which consists of 11 polymer melts. To these is added ethylene monomer, analyzed earlier by Nies et al. by different methods. The numerical values of the scaling parameters differ by at most a fraction of a percent from those in the earlier computations and enhance the accuracy of fit but slightly. The significant improvement over the consecutive procedure (analysis of atmospheric pressure isobar, followed by isotherms at elevated pressures), seen earlier, continues therefore. The scaling parameters so obtained should represent the ultimate in computational accuracy consistent with a specified experimental accuracy. This may have a bearing ultimately on the issue of modeling molecular characteristics, expressed through the scaling parameters, versus macroscopic properties. Using the parameters determined here, it is shown that the entropy is correlated with the scaling temperature and that the flexibility parameter is related to polymer complexity.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1985-1993 
    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: The method of additive properties was used to calculate the dynamic mechanical relaxation time for a series of polyurethanes. Calculations were also made of density and glass transition temperature. Group contributions for nine component groups were determined. With these group values, the densities of the 12 polymers used to determine the groups were calculated and found to agree with measured values within an average of 0.2%. Calculated glass transition temperatures also agreed with measured values within 0.2%. The relaxation time, defined as a parameter in the Havriliak-Negami equation, was shown to be correlated with the glass transition temperature, allowing relaxation time to also be expressed as an additive property. Calculated logarithms of relaxation times agree with measured values to within 7% over a range of relaxation times covering many decades. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 8
    Publication Date: 1984-09-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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  • 9
    Publication Date: 1984-01-01
    Print ISSN: 0362-546X
    Electronic ISSN: 1873-5215
    Topics: Mathematics
    Published by Elsevier
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  • 10
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