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  • Chemistry  (38)
  • Biochemistry and Biotechnology  (1)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 1729-1729 
    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
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 335-342 
    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: Linear 1,2-polybutadiene, glass transition temperature (Tg) -18°C, is crosslinked at -10°C, to -20°C by γ irradiation while strained in simple extension, with extension, ratios (λ0) from 1.2 to 2.7. After release, the sample retracts to a state of ease (λs) at room temperature. From equilibrium stress-strain measurements up to a stretch ratio relative to the state of ease (Λ) of 1.2, together with λ0 and λs, the concentration of network strands terminated by trapped entanglements (νN) is calculated. For this purpose, a three-constant Mooney-Rivlin formulation is used, in which the entanglement network is described by Mooney-Rivlin coefficients C1N and C2N, whereas the crosslink networks is described by the coefficient C1x only. The ratio ψN = C2N/(C1N + C2N) is estimated from parallel studies of nonlinear stress relaxation of the uncrosslinked polymer, taking into account the thermal history before and during irradiation. For substantial degrees of crosslinking, i.e., for R0′ = νx/νN 〉 0.4 (where νN is the concentration of network strands terminated by crosslinks), and for λ0 〈 1.8, C2N agrees rather well with the value obtained from stress relaxation of the uncrosslinked polymer in the range of time scale where it is nearly independent of time (1.87 X 105 pascals). The corresponding value of νN is 2.3 × 10-4 moles/cm3, in good agreement with that obtained from viscoelastic measurements of the uncrosslinked polymer in the plateau zone (2.5 × 10-4). However, for R0′ ≅ 0.2, smaller values of C2N and νN are obtained, indicating that for low degrees of crosslinking the entanglements are not completely trapped. Also, for higher values of λ0, C2N and νN turn out to be somewhat smaller. Similar, less extensive results were obtained previously on a 1,2-polybutadiene with somewhat higher vinyl content and a higher Tg. Crosslinked samples of both these polymers were subjected to equilibrium stress-strain measurements in simple elongation from the state of ease at higher strains up to Λ = 1.7. The results agreed closely with calculations from the three-constant Mooney-Rivlin theory.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 267-271 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Linear 1,2-polybutadiene is cross-linked near its glass transition temperature by γ-irradiation while strained in simple extension with a stretch ratio λo. After release, the sample retracts to a state of ease (λs). From λo, λs, and stress-strain measurements in extension from the state of ease, the concentrations of network strands terminated by trapped entanglements (vN) and by cross-links (vx) can be calculated. For vx/vN ≡ R′o 〉 1, retraction to the state of ease is rapid. For R0o ≃ 0.3 or less, retraction is slow and extends over many logarithmic decades of time scale. When an eased sample is stretched to λo where the cross-links do not contribute to stress, the subsequent stress relaxation of the entanglement network toward equilibrium is also very slow if R′o is small. The slow timedependent processes are attributed to a high proportion of untrapped entanglements on dangling branched structures. The concentration of trapped entanglement strands, vN, can also be calculated from the equilibrium stress at λo. The fraction of trapped entanglements agrees rather well with the predictions of the theory of Langley.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 783-790 
    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 diffusion of radioactively tagged n-hexadecane, n-dotriacontane, and a polybutadiene oligomer with molecular weight 1600 has been studied in 12 rubbery polymers. Diffusion coefficients were obtained from the theory for the thin smear method: for n-hexadecane and for n-dotriacontane (with one exception), in the form appropriate for a completely miscible polymer-penetrant pair, and for the oligomer in the form appropriate for slow entry of the penetrant across the penetrant-polymer interface. For the four flexible linear penetrants, n-dodecane, n-hexadecane, n-dotriacontane, and oligomer, the ratios of diffusion coefficients (or translational friction coefficients) are nearly the same in every polymer. It is concluded that these penetrants travel with similar segmentwise motions, although that is not the case with bulkier, more rigid penetrants. For the three normal paraffins, the friction coefficient is approximately proportional to molecular weight, but that for the oligomer is smaller than would be predicted on this basis.
    Additional Material: 3 Ill.
    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 21 (1977), S. 1729-1729 
    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
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 26 (1984), S. 191-193 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 193-202 
    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: A method is outlined for estimation of small degrees of long-chain branching in polymers with moderately narrow molecular weight distribution (M̄w/M̄n 〈1.4). The storage and loss shear moduli, G′ and G″, are measured in dilute solution by the Birnboim-Schrag multiple-lumped resonator and extrapolated to infinite dilution, choosing a suitable solvent viscosity and frequency range such that the data lie in the terminal zone where G′ and G″ are proportional to the second and first powers of frequency, respectively. The intrinsic reduced steady-state shear compliance is determined from these data and corrected for moderate molecular weight heterogeneity (assuming a Gaussian distribution) from knowledge of M̄w/M̄n and the Mark-Houwink exponent a. The resulting value of S2/S12 (where S1 = Στp/τ1, S2 = Σ(τp/τ1)2, the τp's being the relaxation times and τ1 the longest one) is compared with values calculated by the Zimm-Kilb theory as evaluated by Osaki for comb polymers of regular geometry and different numbers of branch points. The method has been illustrated by measurements on four ethylene-propylene copolymers. One containing no termonomer and one containing a saturated termonomer appeared to be linear; two containing unsaturated termonomers showed small degrees of branching. The method appears to be promising for detecting from one to four branch points per molecule.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 773-781 
    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 diffusion of radioactively tagged n-hexadecane, 1,7-heptanediol, and ethylene glycol has been studied in one polar and six nonpolar rubbery polymers. The penetrant-polymer pairs included some in which the two components were miscible in all proportions and some in which they were nearly incompatible (solubility of penetrant in polymer of the order of 1%). The theory for the thin smear method for measuring the diffusion coefficient was evaluated for incompatible pairs with two cases: case 2, when the rate-limiting step is diffusion through the polymer; and case 3, when the rate-limiting step is entry into the polymer across the penetrant-polymer interface. They are easily distinguished experimentally from each other and from case 1, which refers to completely miscible pairs. In examples of case 3, e.g., ethylene glycol with butadiene or styrene-butadiene rubbers, the half-time for saturating the polymer surface in contact with the penetrant was found to be several days at 25°C. The diffusion coefficients, when compared in four hydrocarbon rubbers, of n-hexadecane and 1,7-heptanediol were similar in magnitude even though in each rubber the hexadecane was soluble in all proportions and the diol only very slightly. The diffusion coefficient of ethylene glycol, despite its extreme thermodynamic incompatibility, appeared to be somewhat larger than those of the other penetrants.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 467-476 
    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 diffusion of radioactively tagged n-hexadecane in trace amounts has been studied in 22 random styrene-butadiene (SBR) copolymers with different styrene contents and butadiene microstructures; in several SBR block copolymers with different average block lengths (also diffusion of tagged 1,1-diphenyl ethane); in a triblock SBR copolymer cast from different solvents and also molded at elevated temperature; and in cis-polybutadiene filled to different extents with carbon black, calcium carbonate, and microglass spheres. The diffusion coefficient in random SBR copolymers decreased with increasing content of styrene and/or vinyl configuration and could be correlated with fractional free volume on the basis of linear additivity of the cis, trans, vinyl, and styrene moieties. In SBR block copolymers, the diffusion coefficient increased with increasing average block sequence length. For the triblock copolymer, the diffusion coefficient was approximately the same for samples molded or cast from solvents which are good for polybutadiene, but was far smaller for a sample cast from ethyl acetate, in which the polystyrene domains are probably lamellar. The effect of fillers on diffusion in cis-polybutadiene was compared with calculations on the basis of several theoretical models.
    Additional Material: 4 Ill.
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  • 10
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of activated fibrinogen takes place in two stages. First, the monomer units form intermediate polymers with twice the original cross-section area and about eight times the original length. The polymers have been detected under a variety of conditions between pH 6.1 and 10. The polymerization geometry is believed to be lateral dimerization with a staggered configuration, determined by a pattern of electrical charges. The negatively charged groups, though unidentified, appear to be near histidine residues, as deduced from the dependence of polymerization on pH. The positively charged groups, from this and other evidence, appear to be α-amino groups. Second, the intermediate polymers unite to form the strands of the fibrin network. This association appears to involve nonpolar groups, and the width of the final strands, unlike that of the intermediate polymer, depends markedly on the net charge as determined by the pH.
    Additional Material: 3 Ill.
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