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  • 1990-1994  (22)
  • 1950-1954  (3)
  • Polymer and Materials Science  (25)
  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 323-328 
    ISSN: 0887-624X
    Schlagwort(e): CF4 plasma ; trimethylolpropane triacrylate ; excited states ; plasma induced polymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The F and CF2-CF2+ excited states have been detected by emission spectroscopy in CF4RF plasmas used for TMPTA polymerization. These excited states are related through electron collision to F and CF2 ground states. The temporal variation of the F and CF2-CF2+ radiative states near the substrate reveals that the F atoms disappear first by incorporation in the monomer during the polymerization phase and, then, by a third body recombination process enhanced by the polymer surface. The CF2-CF2+ radiative states are varying as the inverse of the F states indicating a strong destruction mechanism of CF2 radicals by F atoms.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1155-1161 
    ISSN: 0887-624X
    Schlagwort(e): adsorption ; desorption ; association ; polystyrene ; NMR ; polymer transitions ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Composition-studies were carried out in which samples of films composed of poly(styrene-co-divinylbenzene) particles enmeshed by poly(tetrafluoroethylene) fibers were saturated with dichloromethane and then allowed to evaporate at 23°C to virtual dryness as the 1H-NMR signals and residual weight of sorbed liquid were monitored. The correlations, of 1H-NMR line-widths with the corresponding log of the number, αt of residual sorbed molecules per monomer unit show that sharp changes occur as αt passes through αG the composition that exists when all the liquid not sorbed (i.e., not present within the liquid-saturated particles), has been eliminated, and again as αt passes through αg the composition that exists when the particles attain the rigidity characteristic of the glassy state. Correlation of the corresponding T1 relaxation times with log αt show that sharp changes occur when αt becomes equal first to α′s and then to α′g the compositions that exist respectively when, firstly, all the sorbed liquid not immobilized by adsorption to the polymer chains within the particles has been eliminated, and then when the desorption of immobilized liquid from the chains causes the composition to begin to undergo transition from its rubbery state to its glassy state.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2049-2056 
    ISSN: 0887-624X
    Schlagwort(e): metallocenes ; olefin polymerizations ; Ziegler-Natta catalysts ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Propylene was polymerized with rac-ethylene-bis (1-η5-indenyl)dichlorozirconium/methylaluminoxane in solvents of different polarity. The poly (propylene) formed was separated by solvent extraction; 13C-NMR and DSC measurements were made on the polymer fractions. The poly(propylene) in each solvent fraction has its characteristic molecular weight steric pentad distributions, melting transition temperature, and enthalpy for fusion irrespective of the polymerization medium. The results suggest that the medium dielectric constant does not affect the polymerization rate or the intrinsic stereoselectivity, propagation and chain transfer rates a given catalytic species but can alter the occurrence of steric insertion errors through shifting of distributions of the propagating species producing poly(propylenes) of different stereoregularities. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In the solid phase preparation of synthetic peptide libraries, equimolarity of the resultant peptides in the mixture simplifies the identification of active compounds. Two primary methods for the preparation of combinatorial peptide mixtures are currently used. In the first method, the starting resin is divided into equal aliquots, individual amino acids are coupled to each aliquot, and the resin is then recombined. This process is repeated for each position. However, due to the physical process, each resin bead contains only one peptide sequence. Statistically, for mixtures of longer sequences, an ever-increasing amount of resin is necessary to ensure complete representation of each peptide in the library. Thus, each peptide will be represented in the library if a sufficient number of resin beads are used. In addition, the concentration of each peptide in the library depends on both the number of mixture positions in the library and the amount of resin used. In the second method, mixtures of amino acids are coupled simultaneously at each addition step. The proportion of each amino acid in the reaction mixture is varied inversely to its reaction rate such that, ideally, an equimolar mixture of each peptide is synthesized. An advantage of this method over the previous method is that each peptide is ensured to be represented in the library, although not necessarily in equimolar amounts. It is known that not only do the coupling rates of each amino acid vary, but the coupling rates of individual amino acids also change when coupled to different amino acid resins. Consequently, in order to obtain equimolar peptide mixtures through the use of mixtures of protected amino acids, the ratio of reaction rates of one amino acid over another must be constant irrespective of the resin-bound amino acid. If this premise is true, this method of synthesis offers a significant advantage over the previous method since, theoretically, equimolar peptide libraries could be synthesized. The influence of the resin-bound amino acid on the relative reaction rates of incoming amino acids was investigated in the current study. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 32 (1992), S. 145-159 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Base-stacking and phosphate-phosphate interactions in B-DNA are studied using the finite difference Poisson-Boltzmann equation. Interaction energies and dielectric constants are calculated and compared to the predictions of simple dielectric models. No extant simple dielectric model adequately describes phosphate-phosphate interactions. Electrostatic effects contribute negligibly to the sequence and conformational dependence of base-stacking interactions. Electrostatic base-stacking interactions can be adequately modeled using the Hingerty screening function. The repulsive and dispersive Lennard-Jones interactions dominate the dependence of the stacking interactions on roll, tilt, twist, and propeller. The Lennard-Jones stacking energy in ideal B-DNA is found to be essentially independent of sequence.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2049-2053 
    ISSN: 0887-6266
    Schlagwort(e): empirical gel fraction analysis ; application of Wanxi equation to polyethylenes irradiated in the presence of acetylene and in-vacuo ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Gel fraction data from linear low-density polyethylene (LLDPE) films and high-modulus polyethylene (HMPE) fibers, which had previously failed to give reasonable results when treated with Charlesby-Pinner and Saito-Kang-Dole theory, have been fitted to a modified form of the Wanxi equation. The fitting yields parameters that compare very well with literature values derived by the Wanxi equation, confirming that fracture and cross-linking densities are proportional to a power function (β) of the radiation dose. Extrapolated G(S) values have been obtained from LLDPE using the fit parameters and UV-Vis spectroscopy data. A brief synopsis of the empirical analytical methods available for gel fraction analysis is given. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 581-588 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polyurethanes based on methylene bis(p-phenyl isocyanate), bis(hydroxymethyl) propanoic acid, and poly (tetramethylene oxide) were synthesized, and their morphology and physical properties investigated. The acid polyurethanes exhibited very poor phase separation and mechanical properties, but upon neutralization with alkali metals phase separation improved dramatically and the materials resembled tough elastomers. The choice of cation played a much less important role than hard segment content in determining morphology and properties. Small-angle x-ray scattering patterns of these ionic polyrethanes exhibit two peaks, one characteristic of scattering between the hard and soft domains and the other reflecting scattering from aggregates of ionic groups residing within the hard domains. While ionic aggregation is the primary driving force for phase separation in these materials, their morphology more closely resembles that for nonionic polyurethanes than that for conventional ionomers, because the ionic groups exist in blocks composed primarily of rigid diisocyanate residues.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    ISSN: 0887-6266
    Schlagwort(e): FT-IR ; step-scan interferometry ; 2D-IR ; polyethylene ; rheo-optical characterization ; time-resolved vibrational spectroscopy ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Dynamic mechanical analysis coupled with polarized step-scan FTIR transmission and two-dimensional correlation analysis (2D FTIR) has been used to monitor the submolecular orientational responses of the components of a semicrystalline 50 : 50 blend of low-density polyethylene (LDPE) and perdeuterated high-density polyethylene (d*-HDPE) to a small amplitude uniaxial 23.47 Hz sinusoidal mechanical strain. Perdeuteration of the HDPE component allowed the distinction of its response from that of the LDPE in the blend samples. The experiments were carried out at room temperature. Analysis of the data indicates that the crystalline parts of the two components reorient at different rates, with the functional groups of the high-density portion reorienting faster, in general, than those of the LDPE in response to the mechanical strain. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 625-637 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Three hydrolyzed-starch-polyacrylonitrile (HSPAN) copolymer materials tested as gel-water dispersions in a Brookfield rotating spindle viscometer exhibited velocity slip at solid boundaries and a yield stress. Dispersions with 0.5% HSPAN concentrations were about 20,000 times more viscous than water when the shear stress surpassed the yield stress and viscous power-law flow ensued. The apparent viscosity of an HSPAN gel-water dispersion was reduced by nearly an order of magnitude when tap water was substituted for deionized water. The apparent viscosity of the HSPAN gel-water dispersions decreased by about 30% after the fluid was continuously maintained at a temperature of 80°C for 1 week, and by an order of magnitude or more after 3 weeks under those conditions. In natural convection tests, the yield stress enabled an HSPAN gel-water dispersion to withstand greater temperature differences across a horizontal layer before inception of natural convection than a fluid without one. © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 569-575 
    ISSN: 0887-6266
    Schlagwort(e): polymer blend ; ionomer ; sulfonated polystyrene ; poly(2,6-dimethyl 1,4-phenylene oxide) ; miscibility ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Zinc-neutralized sulfonated polystyrene ionomers (ZnSPS) and poly(2,6-dimethyl 1,4-phenylene oxide) homopolymer (PXE) form miscible blends up to at least 7.8 mol % sulfonation, as measured by thermal and mechanical criteria. The addition of an equal weight of PXE raises the glass transition temperature of ZnSPS by 40-50°C. However, this miscibility is not achieved by eradicating the microdomain structure present in ZnSPS, even though the PXE coils are considerably larger than the spacings between ionic aggregates. Small-angle x-ray scattering indicates that while the average interaggregate spacing is roughly the same in ZnSPS and its 50/50 blend with PXE at a given sulfonation level, the extent of phase separation is reduced upon PXE addition, indicating that more ionic groups are dispersed in the matrix. Factors influencing miscibility in the ZnSPS/PXE materials and related blends are discussed.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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