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  • Wiley-Blackwell  (17)
  • American Association for the Advancement of Science (AAAS)
  • 1995-1999  (17)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 490-496 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: We have derived a new deconvolution formula to obtain the original no-loss XPS spectra, the so-called source function, by taking surface effects into account. With this formula the primary XPS spectra of Au 4d and Au 4f are carried out from the experimental data. The primary excitation spectra are compared to the results derived by Tougaard’s method in which surface effects were neglected. The present result is markedly different from Tougaard’s result, which consists of a tail extending ∽50 eV below the peak. The result reveals that the influence of surface effects on the background removal of the spectra is considerably significant for the energy range ∽50 eV below the peak energy. It is also found that the large tail in Tougaard’s results can be essentially removed when surface effects are considered.
    Additional Material: 7 Ill.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We carry out temperature-dependent lattice dynamics calculations to determine the vibrational normal modes associated with the interbase H-bond breathing motion in several B-DNA copolymers at temperatures from room temperature to the melting temperatures. We take into consideration Raman selection rules and incorporate a simple empirical model of Raman susceptibility in the interbase H bonds in our calculation and compare them to Raman measurements. Our calculations are carried out using empirical force constants that are not further refined to low-frequency spectra. Our calculations show the existence of strong interbase H-bond breathing modes at frequencies and with relative oscillator strengths close to the observed Raman peaks in the range of 60-140 cm-1 for the DNA sequences considered except for one helix. The correlation between the calculated and observed frequencies and oscillator strengths indicates that the observed Raman peaks in the frequency range are likely interbase H-bond breathing modes. We find that these modes exhibit sizable temperature as well as sequence dependence. We show the softening of these modes on approaching thermal denaturation that is also in agreement with the observed behavior in Raman and melting measurements. The sensitivity of the calculation on the empirical model of Raman susceptibility and the possible reasons for the discrepancy between a few calculated values and observations are discussed. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 35 (1995), S. 657-666 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Calculations of the normal mode spectrum of a netropsin-DNA complex, an isolated DNA helix of the same sequence, and a free netropsin molecule were carried out and compared with observations. We find that the frequency of modes of the complex that are primarily vibrations localized to the helix are relatively unchanged from the frequencies found for similar modes of the isolated helix. On the other hand, the frequencies of those modes of the complex that are found to be primarily in the netropsin are found to change significantly in the complex from that of the free netropsin. Further analysis indicates that the changes in the “netropsin modes” are primarily due to the conformational deformation induced in the netropsin by formation of the complex. All the frequencies and shifts in frequency are in good agreement with recent Raman measurements. © 1995 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2613-2620 
    ISSN: 0887-624X
    Keywords: polydimethylsiloxane ; poly(methyl methacrylate) ; block copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Azo group-containing polydimethylsiloxanes (PDMS-ACP), macroazoinitiators, were prepared by polycondensation reaction of 4,4′-azobis-4-cyanopentanoyl chloride (ACPC) with hydroxybutyl-terminated polydimethylsiloxane (PDMS) of varying molecular weights. The activation energy (Ea), activation enthalpy (ΔH
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 1025-1036 
    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 phenomenological model developed describes the steady-state sensing characteristics of a biosensor based on biooxidation of organic solutes by dissolved oxygen. The model is experimentally verified using a recently developed dopamine sensor that enzymatically oxidizes dopamine by polyphenolase in apple tissues. It adequately describes its steady-state sensing characteristics, including the effects of mass of immobilized apple fines in the biofilm, temperature, and pH of the substrate solution. The parameters provide a basis for evaluating the suitability of different bioactive materials or the same bioactive material from different sources for biosensor fabrication. At zero thickness of the membranes and biofilm, the model describes the sensing characteristics of a dissolved oxygen probe in which the oxygen diffusivity through the Teflon membrane is 9.83 × 10-11 m2/s, comparable with a previously reported value. It can also describe the sensing behavior of any nonbiocatalyzed oxidation-related sensor in a two-substrate system simply by replacing the governing faradaic equations for the dissolved oxygen probe with those appropriate to the type of probe used.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 2661-2663 
    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: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Communications in Numerical Methods in Engineering 12 (1996), S. 497-505 
    ISSN: 1069-8299
    Keywords: weight function approach ; edge crack problem ; Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: A fundamental field for the edge crack problem is suggested, and the field is composed of the singular displacement field and the complementary regular field. The boundary displacement of the fundamental field plays the role of the weight function in the edge crack problem. After multiplying the boundary traction in the physical problem with the weight function and performing integration along the boundary, the stress intensity factor at the crack tip is obtainable. Numerical examples are given to demonstrate the use of the suggested weight function approach.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 42 (1997), S. 771-781 
    ISSN: 0006-3525
    Keywords: secondary structure ; CD spectroscopy ; ion channel ; double-helical conformations ; solvent polarity ; conformational change ; polypeptide structure ; nonaqueous solvents ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solvent effects on the far-uv CD spectra of the polypeptide gramicidin have been studied systematically in a series of alcohols of increasing chain length, ranging from methanol to dodecanol. The effects observed are of two types: primary, involving a change in the equilibrium mixture of conformers present, and secondary, involving a shift in the spectral peak positions as a function of solvent polarizability.To quantitate the primary effect, the ratio of the individual conformers present was estimated by deconvolution of the spectra into their component species. For short chain length alcohols, both parallel and antiparallel double helices are found in considerable abundance. As the solvent chain length is increased and its polarity is decreased, the left-handed antiparallel double helical species is favored. For all alcohols with chain lengths of four or more carbon atoms, the ratio of the conformers present remains relatively constant.To quantitatively examine the secondary effect, the magnitudes of the spectral shifts on the dominant conformer (species 3) have been correlated with the dielectric constants and refractive indices of the solvents, thereby indicating what underlying physical properties are responsible for these shifts.This work thus demonstrates that for gramicidin, a flexible polypeptide, the solvent effects on the CD spectra can be resolved into two types: changes due to the mixture of conformers present and shifts in the spectral characteristics. Both effects need to be considered when interpreting CD spectra in terms of secondary structure for this and other polypeptides in nonaqueous solutions. © 1997 John Wiley & Sons, Inc. Biopoly 42: 771-781, 1997
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Communications in Numerical Methods in Engineering 13 (1997), S. 655-663 
    ISSN: 1069-8299
    Keywords: stress intensity factors ; computing compliance method ; Engineering ; Numerical Methods and Modeling
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: For a cracked orthotropic torsion bar, the torsion compliance C is evaluated numerically in this paper. The dependence of the compliance C with respect to the crack length A will give the stress intensity factor at the crack tip. Numerical examples are given to demonstrate the influence of the elastic material constants of orthotropic materials. ©1997 John Wiley & Sons, Ltd.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 585-594 
    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: Several carboxylated poly(butyl acrylate) latices prepared by a semibatch emulsion poly-merization process were characterized in this study. A significant amount of polyelectrolyte was found in the latex product containing 10% AA, designated as AA10. On the other hand, latices containing 0.1% AA (AA0.1), 0.1% MAA (MAAC.1), and 10% MAA (MAA10) showed very low levels of polyelectrolyte in water. Based on the critical flocculation concentration data, it can be concluded that incorporation of 10% AA or 10% MAA into the emulsion polymers can greatly improve the chemical stability of the latex products, especially at higher pH. The data of the pH and conductometric titration experiments show that the MAA unit can be distributed more uniformly in the latex particles in comparision with the AA unit. This result is further confirmed by determination of the Tg's of the emulsion polymers by means of thermally stimulated current (TSC). © 1996 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
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