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  • Polymer and Materials Science  (658)
  • Life and Medical Sciences  (98)
  • Genetics
  • ASTROPHYSICS
  • Wiley-Blackwell  (756)
  • 1965-1969  (756)
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Keywords
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  • Wiley-Blackwell  (756)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Infrared and nuclear magnetic resonance of maleic anhydride copolymers and their half esters (1968)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 2191-2200 
    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: Infrared and NMR group-type methods for the analysis of the anhydride content of maleic anhydride copolymers such as poly(maleic anhydride-co-α-olefin) and the half ester content of their reaction products with alcohols are described. The infrared analyses are based on the integrated absorptivities of the anhydride carbonyl and the combination of the acid and ester carbonyl. The NMR method is based on the intensities of the various chemically shifted groups in the copolymer. The use of dimethyl sulfoxide as an auxiliary solvent has made the infrared analysis possible.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1968.070121001
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  • 2
    Electronic Resource
    Electronic Resource
    Panel discussion: Present status and perspectives in the study of cytodifferentiation at the molecular level. II. Discussion (1968)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 72 (1968), S. 219-230 
    Details
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jcp.1040720415
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  • 3
    Electronic Resource
    Electronic Resource
    Poly(arylene sulfones) prepared by friedel-crafts reactions (1967)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 1802-1804 
    Details
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1967.150050728
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  • 4
    Electronic Resource
    Electronic Resource
    Chemically reacting systems of the type A + B ⇄ AB. II. Osmometry (1969)
    New York : Wiley-Blackwell
    Biopolymers 7 (1969), S. 5-19 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The osmotic pressure equation for nonideal, associating systems of the type nA +mB ⇄ AnBm, has been derived, by using the assumption yAnBm/yAnyBm = 1. This treatment can also be applied to related associations such as nA + mB ⇄ AB + AB2 + A2B + …. From osmotic pressure experiments on the pure reactants it is possible to obtain the molecular weights (MA and MB) of the reactants and also the virial coefficients (BAA and BBB) of the reactants. The osmotic pressure of a nonreacting mixture of A and B can be calculated from these measurements. It can be used along with osmotic pressure measurements on equilibrium mixtures of A and B to obtain expressions containing the equilibrium constant (or constants) and the cross-virial coefficients (BAB and BBA). Several procedures are described for the evaluation of the equilibrium constant (or constants) and the BAB or BBA terms. It appears that this procedure is a general one which is applicable to associations of the type nA + mB ⇄ AB + A2B + AB2 + …. By correcting for nonideal behavior, one should then be able to apply it to any method available for analyzing ideal associations of the types considered here. In addition it is possible, subject to certain restrictions, to analyze associations of the type 3A + B ⇄ A2 + AB.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1969.360070103
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  • 5
    Electronic Resource
    Electronic Resource
    Some rheological properties of molten polypropylene (1968)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 871-883 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The following measurements were carried out on the melts of two samples of polypropylene, one with a narrow and one with a broad molecular weight distribution: viscosity in steady shear flow, dynamic storage and loss moduli, total normal thrust in cone-and-plate apparatus, and flow birefringence. The validity of various theoretical interrelations between the measured quantities is checked. The influence of molecular weight distribution is qualitatively discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1968.160060507
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  • 6
    Electronic Resource
    Electronic Resource
    Effect of stereosequence length on crystallization kinetics of propylene oxide polymersPresented to the Division of Polymer Chemistry, 150th American Chemical Society Meeting, Atlantic City, N. J., September 1965. (1966)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 715-729 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crystallization kinetics of crystalline fractions of propylene oxide polymers made with different catalysts have been studied by isothermal dilatometric and microscopical measurements. Isothermal microscopical measurements indicate that spherulite growth in these polymers proceeds from predetermined nuclei. The half time for spherulitic appearance is less than, but of the same order as, the half time for complete crystallization. Only by taking this factor into account can the dilatometric data be represented by the Avrami equation. The deviation of the crystallization isotherm from that predicted from the microscopical data using the Avrami theory is attributed to a secondary crystallization process taking place within the spherulite. Crystallization continues long after spherulites completely occupy the available volume in the polymer. By assuming that the secondary crystallization proceeds as a first-order process in the uncrystallized, but crystallizable, portions of the melt, it is shown that the crystallization isotherms can be completely described in terms of four parameters. These are: (1) the time constant for the primary crystallization process; (2) the time constant for nucleation; (3) the time constant for the secondary crystallization process, and (4) the extent of secondary crystallization. The important conclusions of these studies are: the rates of nucleation and of spherulitic growth are far more dependent on temperature than on stereoregularity; the ratio of the rate of the secondary crystallization process to that of the primary crystallization process is almost independent of temperature, but increases with increasing stereoregularity of the polymer.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1966.160040505
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  • 7
    Electronic Resource
    Electronic Resource
    Temperature dependence of the growth rate of spherulites (1968)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 165-180 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spherulitic growth data that exist in the literature for a wide diversity of polymers have been analyzed according to various possible nucleation mechanisms. It is demonstrated that, if allowed a reasonable choice for the equilibrium melting temperature, no unbiased selection of a unique nucleation process can be made. Moreover, a set of universal parameters exists for each of the allowable nucleation processes which enables the data to be represented by a single straight line which encompasses all the polymers. The only quantities specific to a given polymer are the equilibrium melting temperature and the activation energy for transport. The magnitude of the latter quantity is shown to be dependent on the glass temperature of the polymer.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1968.160060109
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  • 8
    Electronic Resource
    Electronic Resource
    The steady flow shear modulus of polymer meltsProd. No. 1277 (1966)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 75-80 
    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: Relaxation times of polyethylene melts have been measured by Aloisio, Matsuoka, and Maxwell. One implication regarding their observations is that the elastic properties of polymer melts must be time-dependent. In particular, the steady-flow shear modulus depends on the strain rate. Some interpretations of data in the literature have been based on concepts in rubber elasticity where the steady-flow modulus is an equilibrium value, independent of strain rate. We have used Pao's theory for viscoelastic flow together with measurements of relaxation times to discuss the strain rate dependence of the steady-flow shear modulus of melts. The existence of a strain rate-dependent shear modulus leads naturally to a nonlinear relation between shear stress and recoverable shear strain. The conclusions regarding the molecular weight dependence of the modulus also differ from interpretations based on rubber elasticity.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1966.070100105
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  • 9
    Electronic Resource
    Electronic Resource
    The influence of intermolecular hydrogen bonding on the flow behavior of polymer melts (1969)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 2721-2733 
    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: The influence of hydrogen bonding on the flow behavior of polymer melts at high shear rate has been investigated using a capillary extrusion rheometer. The systems studied were copolymers of ethylene and acrylic or methacrylic acid. Hydrogen bonding was found to substantially enhance both flow activation energy and viscosity level, as well as the degree of dependence of viscosity on rate of shear. It was also found that hydrogen bonding does not influence the critical shear stress for onset of “melt fracture.” The data support the view that hydrogen bonds act effectively as temporary (quasi-) crosslinks during the short time scales of deformation involved in flow at high shear rates.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1969.070131219
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  • 10
    Electronic Resource
    Electronic Resource
    Raman spectrum of the right-handed α-helix of poly-L-alanine (1969)
    New York : Wiley-Blackwell
    Biopolymers 8 (1969), S. 167-171 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The laser-excited Raman vibrational spectrum of poly-L-alanine has been obtained. The Raman spectrum is compared with the infrared spectrum and vibrational frequencies calculated from normal coordinate analysis. The symmetric modes of the α-helix appear with strong intensity in the Raman spectrum. A large number of skeletal modes are obtained in this Raman spectrum for the first time.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1969.360080203
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