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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 2 (1979), S. 69-70 
    ISSN: 0935-6304
    Keywords: Gas Chromatography ; Stationary phases, chemical stability in solutions ; SE 30, SE 54 in chloroform or toluene show rapid depolymerization (HCL-, Tetramethylammoniu hydroxide-traces responsible) ; Solutions with decreased molecular weight of silicon phase give decreased film thickness (Hg plug technique) and increased tailing in glass capillary impregnation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 2 (1979), S. 405-410 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Stationary phases of polysiloxane-type degrade in acidic solution ; Several salt traces affect stability at high temperature NaCl on Duran-5O: no effect at 260°C ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of polysiloxanes have been shown to be sensitive to acids when dissolved in chloroform.At 26O°C polysiloxanes were found to degrade under the influence of several compounds used or produced during the preparation of glass capillary columns.
    Additional Material: 6 Ill.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(L-valine) (PLV) belongs to the class of polyamino acids having a bulky side chain. It preferably adopts the β-sheet conformation, although high molecular weight PLV may form an α-helix as well. In the present article we report a detailed study of the phonons and their dispersion for β-PLV and the spectra of oligovalines in relation to its polymeric form. The N-deuterated analogue of β-PLV has also been studied to check the correctness of assignments and force field. Density of states and heat capacity have been obtained. The heat capacity is in very good agreement with the experimental measurements of Roles et al. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 12 (1973), S. 1377-1385 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using Wilson's GF-matrix method as modified by Higgs for infinite helical polymers, dispersion curves and the frequency distribution function have been calculated for poly-L-proline II chain. Infrared spectrum is obtained and a Urey-Bradley force field, which provides best fit with the observed frequencies, is evaluated. The result are discussed from the viewpoint of the conformational characteristics of forms I and II.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 1987-1990 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 657-678 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: On axial extension of polymer melts at constant deformation rates, the development of high-elastic deformation is of predominant importance during the initial period. High-elastic deformation is accompanied by a rise in viscosity and in the modulus of high-elasticity and by retardation of the relaxation processes in the region of large relaxation times. At relatively low deformation rates, the rise in viscosity and high-elasticity modulus and the retardation of relaxation processes may give way to a decrease in viscosity and high-elasticity modulus and acceleration of relaxation processes, so that stationary flow regimes are attained. The transition from strain regimes with increasing viscosity and modulus of high elasticity to those with a decrease of these quantities corresponds to an increase in the rate of accumulation of irreversible deformation. Accordingly, a competing influence due to the orientation effect and to destruction of the network of intermolecular bonds becomes evident while stationary flow is being attained. The orientation effect must be responsible for the retardation of the relaxation processes, whereas rupture of the intermolecular network bonds results in structural relaxation accelerating relaxation processes. In contrast to shearing, during extension the orientation effect is of predominant importance. Hence in stationary flow regimes the viscosity may not only remain independent of the rate of strain, but even increase with it. In this case the contribution of the large relaxation times to the relaxation spectrum increases with increasing stress in stationary flow regimes. The fact that the longitudinal viscosity and the modulus of high elasticity are independent of the stress in stationary flow regimes does not guarantee linearity of the mechanical properties of the polymer in the prestationary stage of deformation when complex changes occur in its relaxation characteristics. At high deformation rates the viscosity and the modulus of high elasticity keep rising with increasing deformation until rupture occurs. Determination of the strength of polystyrene samples vitrified after extension showed that it is due not to the entire degree of extension, but only to the value of accumulated high-elastic deformation. The strength of the vitrified samples is to a first approximation independent of the rate at which the melt was extended.
    Additional Material: 19 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 3271-3277 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 9-Anthranylmethyl hexafluorophosphate-a stable primary carbenium salt-is prepared and characterized by UV, VIS, and NMR spectroscopy and by conductometric measurements in methylene chloride. 9-Anthranylmethyl hexafluorophosphate initiates the polymerization of vinyl and heterocyclic monomers. This initiator has higher reactivity than trityl and diphenylmethyl salts. The initiation mechanism of the polymerization of some monomers is investigated.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1129-1143 
    ISSN: 0887-624X
    Keywords: adsorption ; desorption ; association ; roto-fluorescence ; probe ; polystyrene ; glass-transition ; polymer transitions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fluorescence intensity and residual weight of poly(styrene-co-divinylbenzene) saturated with a 〈 0.003M solution of a intramolecular-rotor-fluorescent probe-molecule in a volatile liquid were monitored simultaneously as the system evaporated at 23°C to virtual dryness. The “breakpoints” in the pattern for fluorescence increase coincided with the “breakpoints” in the kinetics of desorption with respect to the number, αt of residual sorbed volatile molecules per phenyl group in the polymer, showing that both time-studies reflect the same physical changes in the system that occur reproducibly as αt decreases monotonically through α′s and α′g the compositions that signal respectively incipient elimination of volatile molecules immobilized by adsorption to polymer, and incipient transition of the system from the rubbery state to the glassy state. The fluorescence intensity attained its asymptotic limit before αt became equal to αg the composition identified earlier to be that which marks completion of the transition to the glassy state.
    Additional Material: 11 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3283-3292 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initiation of polymerization of α-methylstyrene and p-methoxystyrene with 9-anthranylmethyl salts proceeds by hydride transfer from the monomer to the initiator. As a result, macromonomers with a double bond as head group are formed. These products polymerize and copolymerize by radical and ionic mechanism leading to graft and block copolymers. Styrene and α-caprolactone polymerize with the same initiator by cationation of the monomer. In this case each macromonomer contains one photoreactive anthranylmethyl group which may photodimerize. As a result copolymers of the type A—A or A—B are produced.
    Additional Material: 2 Ill.
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  • 10
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time studies of evaporation from liquid-saturated poly[(Sty)98-co-(DVB)2] particles enmeshed in poly(tetrafluoroethylene) microfibers show that it is possible to distinguish kinetically between volatile sorbed molecules not absorbed to the polymer chain and those that are adsorbed to it. Elimination of the nonadsorbed molecules occurs first, and it follows zero-order kinetics. The subsequent elimination of the residual volatiles, namely the adsorbed molecules, follows first-order kinetics, with a rate constant that remains constant only until the enmeshed microparticles undergo transition from the gel to the glass state. Thereafter, is observed a sequence of up to six independent rate constants in a series of intervals, the durations of which increase exponentially. This is interpreted to mean that after evaporation to the glass transition composition, the total weight of residual adsorbed molecules is given by a linear combination of exponential decay functions for up to six populations of adsorption sites, the rate constants for which reflect the force of association between the sites and the retained molecules.
    Additional Material: 7 Ill.
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