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  • Polymer and Materials Science  (3,761)
  • SPACE VEHICLES  (1,146)
  • THERMODYNAMICS AND COMBUSTION  (723)
  • 1970-1974  (3,056)
  • 1965-1969  (2,574)
  • 1971  (3,056)
  • 1967  (2,574)
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  • 1970-1974  (3,056)
  • 1965-1969  (2,574)
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  • 101
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The diffusion, sedimentation, and viscosity behavior of native DNA has been studied as a function of molecular weight absolutely determined by diffusion and sedimentation measurements between 106 and 20 × 106 Daltons. Only data for monodisperse subfractions of the polydisperse DNA samples investigated have been compared. They were derived by means of calculations based on individual sedimentation constant distribution and polymer parameters. The inconstancy of these parameters for the semi-rigid DNA molecules over the range of different sub-fractions of the polydisperse samples has been taken into account. A detailed description of the corresponding mathematical background as well as of the diffusion measurements has been given in the two preceding papers. For the homologous series of monodisperse native DNA molecules, three-parameter equations have been determined representing the s0-[η], s0-M, and [η]-M relations as well as the D0-s0 and D0-M interdependence over the entire molecular weight range of interest. Furthermore a simple equation is given describing the molecular weight dependence of the Mandelkern-Flory-Scheraga parameter β in terms of s0 and [η]. The asymptotic value β∞ has been determined, primarily by measurements at finite molecular weights, to be 2.39 × 106, resulting in β values near 2.50 × 106 at M = 108 Daltons. The hydrodynamic properties of our two calf thymus DNA samples of highest molecular weight proved to be influenced by residual protein interactions resulting in a more compact conformation. Further data are given demonstrating the influence of the individual polydispersity of the investigated samples on diffusion constant and molecular weight averages.
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  • 102
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Titration of an aqueous solution of sodium poly-L-glutamate with a strong acid usually produces turbidity and precipitation before the equivalence point is reached. In 1M sodium p-toluenesulfonate and 1M sodium methylcyclohexanesulfonate aggregation was delayed for days to months. In very concentrated tetra-n-butylammonium chloride and bromide the polymeric acid dissolved and could be titrated with NaOH. However, potentiometric titration curves in these solutions did not yield information (by way of plots of apparent pK versus the degree of neutralization) about the helix-to-coil transition of the polymer. It was argued in addition that the apparent pK of a weak polyelectrolyte should not be calculated from titrations in concentrated salt solutions since it is a mixed or composite quantity. It contains not only the effect of the salt on the dissociation of the weak electrolyte but its effect on the activity coefficient of hydrogen ions as well.Circular dichroic spectra were therefore measured a t various degrees of neutralization of poly(L-glutamic acid) in a number of aqueous salt solutions and mixtures of organic solvents with water. It was found that the undissociated polymer in the concentrated methylcyclohexanesulfonate and quaternary ammonium halide solutions had the spectrum of a right-handed α helix. The n → π* band at 222 mμ was used as a measure of the fraction of polymer in the helical conformation. The value of - Δε for the undissociated polyacid in these organic electrolyte solutions was 11.4. By means of this value and a number of assumptions, the fraction of helix (fh) as a function of α, the degree of polyacid neutralization, was calculated for the different solvent mixtures. An empirical equation was used to describe the variation of fh with α, fh = 1/(1 + e-a+bα), in which b represents the degree of cooperativeness of the transition, and a is a measure of the effect of the medium on the onset of the transition. The values of b did not differ very much from one another, suggesting that the cooperativeness of the transition was not sensitive to changes in the medium. On the other hand, the value of a (or its equivalent, the value of α at the halfway point in the transition) was more dependent on the solvent. Comparisons of these results with those of some other workers were made by means of the empirical equation.
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  • 103
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    Biopolymers 10 (1971), S. 411-416 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 104
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    Biopolymers 10 (1971), S. 417-419 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 105
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    Biopolymers 10 (1971), S. 399-410 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of temperature on the binding of 9-aminoacridine and of proflavine to E. coli DNA in 10-3M NaCl solution has been determined by a spectrophotometric technique. The inadequacy of the expression normally used for the determination of the extent of binding is discussed with reference to measurements at temperatures above which dissociation of the double helix occurs. A method of determining the relative extents of binding to native and denatured DNA at elevated temperatures is described.
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  • 106
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    Biopolymers 10 (1971), S. 421-421 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 107
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    Biopolymers 10 (1971), S. 423-423 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 108
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The quantum-mechanical calculations by the PCILO method on the conformation of amino acid residues of proteins have been extended to the valyl, leucyl, and isoleucyl residues. In distinction to the earlier “empirical” computations, the quantum-mechanical results indicate very similar energy contours for the stable conformations of the three residues. Their general outline is also similar to that of the alanyl residue, although reduced by about 25%. Contrary to the “empirical” computations, the present results predict that the region corresponding to the α-helix should be one of great stability for the three residues and in particular for the valyl residue. The quantum-mechanical results are in excellent agreement with the experimental conformations of the aliphatic residues in lysozyme and myoglobin. Their prediction as to the ready availability of the valyl residue in the α-helical conformation agrees moreover with Ptitsyn's statistical evaluation of the participation of this residue in the inner turns of the helical regions in six globular proteins. The maximum conformational space allowed for the aliphatic residues is somewhat smaller than that allowed for the aromatic ones, while the minimum conformational space (region of stability common to all the residues) is similar in both groups.
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  • 109
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    Biopolymers 10 (1971), S. 513-522 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The helix-coil transition of DNA of various base compositions has been followed by measuring the heat capacity and the ultraviolet absorption as a function of temperature through the transition region. The results of these measurements indicate that the transition enthalphy ΔH for a given pH value and salt concentration depends considerably on the base composition of the various DNA samples. The values of the transition enthalpies vary from ΔH = 7.73 kcal/mole base pair (MBP) for 31% GC base pairs to ΔH = 8.52 kcal/MBP for 72% GC base pairs. The results of the heat capacity measurements are discussed in relationship to the theoretical models suggested by various authors. Some peculiarities of the measured heat capacity versus temperature curves are reported. The correlation between these peculiarities and the results of the transcription experiments of DNA is discussed.
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  • 110
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    Biopolymers 10 (1971), S. 711-719 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly-L-histidine (PLH) films at different degrees of protonation were produced mid subjected to infrared spectroscopic investigation (range 4000-650 cm-1). In addition, the N-deuterated film spectra were plotted. The amide II and III bands show that the peptide group is present in the trans form. The amide I and II bands show that at 0% and 50% protonation the PLH occurs as an α-helix and at 100% protonation as a random coil with some ranges in β structure. At 0% and 50% protonation, no hydration water is bound to the backbone. At 0% protonation all NH groups are linked to each other or to water molecules via hydrogen bonds. At 50% protonation NH+ċN bonds form between the imidazole rings. These protons are present in continuous energy level distribution. Such bonds with tunneling protons are extremely polarizable and between these bonds may act proton dispersion forces. The Cl- ions are bonded to the NH groups of the imidazole groups. The hydration water is bonded to the Cl-- ions and to the NH groups. At 100% protonation, hydration water is bonded also to the CO groups of the backbone. The NH groups of the backbone, like those of the rings, endeavor especially in the dry state to bond to the Cl- ions. This leads to a strong steric constraint of the random coil.
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  • 111
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    Biopolymers 10 (1971), S. 721-737 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational transition between the two helical forms I and II of poly-L-proline serves as an experimental model for the study of the kinetic, behavior of cooperative systems. The slow I ⇌ II conversion after a sudden perturbation of the solvent composition was followed polarimetrically. The dependence of the mean relaxation times on chain length and the degree of conversion was compared with Schwarz's theory. In addition, a description of the entire relaxation curves was possible in three special cases: all-or-nothing, small perturbations of the I ⇌ II equilibrium in long chains, and conversions which start off with molecules completely in one or the other conformational state. The mathematical model on which the theory is based contains only one more adjustable parameter than the equilibrium model, but it adapts to the experimental results surprisingly well. The present kinetic results and equilibrium measurements on this system are described by the same values of those parameters which are common to both models. The found value of the rate constant of the propagation step, i.e. the cis ⇌ trans isomerization of a peptide bond at an existing I-II junction, agrees with the rate of isomerization in N,N-dimethylacetamide reported in the literature. The rate of nucleation is up to 105 times smaller than the rate of propagation.
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  • 112
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    Biopolymers 10 (1971), S. 739-751 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The circular dichroism of glycosaminoglycans and ganglioside in distilled water are described, showing two bands in the region of amide and carboxyl transitions. The first, negative hand is common to all polymers and the amino sugar derivatives. The characteristics of the second band depend upon polymer structure. Those containing 4-1-linked amino sugars show a second, positive, resolved band about 190 mμ, while those with 3-1-linked amino sugars show a second, negative band less resolved from the first usually ≤185mμ, but clearly centered at 188mμ for dermatan sulfate. Ultraviolet optical absorption from 300 to ∼183 mμ showed inflection regions around 190 mμ for most compounds.
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  • 113
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of γ-benzyl glutamate NCAs has been investigated. The results indicate that a coil-to-helix transformation is not responsible for the kinetic data. The results were rationalized by assuming formation of polymer aggregates coupled with the stereoselective adsorption of monomer onto growing polymer prior to reaction. From kinetic data a ratio of equilibrium constants for adsorption was determined. Independent data confirmed the assumption that adsorption of monomer onto polymer occurred. Equilibrium constants were evaluated, and their ratio was found to be comparable with that obtained from the kinetic data.
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  • 114
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    Biopolymers 10 (1971), S. 849-863 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A preliminary neutron-scattering study of wet-spun oriented NaDNA samples with various contents of H2O or D2O has been performed to obtain information about the hydration of NaDNA. The preferred orientation was in the direction of the crystallographic c axis. Perpendicular to this direction the samples could be regarded as poly-crystalline. It has been found that the preferred crystallite orientation was also reflected in the water structure. This fact, taken together with the small energy widths of the measured near-elastic peaks indicates that water molecules in the sample are relatively strongly bound to the DNA helix either directly or via other water molecules. Angular distribution measurements of elastically scattered neutrons were performed with the momentum transfer vector directed along and perpendicular to the DNA helix axis. Different Debye-Waller factors were obtained, indicating different water dynamics in the two directions. Comparison between the H2O and D2O measurements suggests that the difference is caused by motions of rotational nature. The shape of the frequency distribution function for the H2O molecules in the NaDNA sample was somewhat similar to that which has been measured in ice.
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  • 115
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    Biopolymers 10 (1971), S. 865-882 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The linear dichroism induced in a solution of electrically anisotropic molecules by a pulsed electric field has been studied. Equations have been obtained which express the dichroism as a function of dipole moment, excess polarizability, field strength, and the angle α between the dipole moment and the transition moment for the absorption band. These expressions have been related to the experimentally observed difference signal in such a way that when the dichroism is measured as a function of field strength the permanent moment, excess polarizability and angle a can be determined.Experiments have been carried out on tobacco mosaic virus (TMV), which is similar in its properties to the theoretical model. The polarizability anisotropy and rotary diffusion constant for the monomer and dimer of TMV have been obtained from these experiments. In addition to the molecular parameters mentioned above, the saturated electric dichroism of the virus was measured as a function of wave length and the presence of an n-π* transition in the tryptophan spectrum was indicated.Further experiments measuring dichroism as a function of pH demonstrated the general denaturation of the virus at high pH (10-11) but also the existence of a stable fraction which is not fragmented even at the high pH involved.
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  • 116
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    Biopolymers 10 (1971), S. 2459-2490 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The binding of Mg ++ to polyadenylate (poly A), Polyuridylate(poly U), and their complexes, poly (A + U) and poly (A + 2U), was studied by means of a technique in which the dye eriochrome black T is used to measure the concentration of free Mg-. The apparent binding constant KX = [MgN]/[Mg++][N], N = site for Mg++ binding (the phosphate group of the nucleotide), was found to decrease rapidly as the extent of binding increased and, at low extents of binding, as the concentration of Na- increased in poly A, poly (A + U), and poly (A + 2U), and somewhat less so in poly U. Kx is generally in the range 104 〉 KX 〉 102. The cause of these dependences is apparently, primarily, the displacement of Na+ by Mg++ in poly U and poly (A + U) on the basis of the similarity of extents of displacement measured in this work and those measured potentiometrically. \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta H'{\rm v}.{\rm H}. = - R(\partial {\rm }\ln Kx/\partial 1/T)_\theta,\theta = \frac{{{\rm Mg}N}}{{N_t }} $$\end{document} was calculated and was found to approach zero as the concentration of Na+ increased. In poly U, poly (A + U), and poly (A + 2U) at low ΔH′ v.H. 〉 0, about + 2 kcal/“mole.” In poly A, also at low salt, ΔH′ v.H. ≈ -4 kcal/“mol” for the initial binding of Mg++, and increases to +2 kcal/“mol” at saturation. This enthalpic variation probably accounts for the anticooperativity in the binding of Mg++ not ascribable to the displacement of Na++.
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  • 117
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    Biopolymers 10 (1971), S. 2581-2590 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High-resolution nuclear magnetic resonance spectra at 100 MHz have been obtained on poly-N-methyl-L-alanine in the chloroform-trifluoroacetic acid system under various conditions of solvent composition. Different spectra are observed for the CH3-Cα, Cα-H, and N-CH3 protons. On the basis of conformational analysis an interpretation of the NMR results was attempted.
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  • 118
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    Biopolymers 10 (1971), S. 2607-2614 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An analysis of optical rotatory dispersion and circular dichroism of RNA is described which leads to an estimate of the degree of base pairing. By the use of new standards for the double-helical parts of the molecule, based on data for two-stranded viral RNA species, a good fit between calculated and observed curves can be achieved. Where data are available the results of analyses of optical rotatory dispersion and circular dichroism in general show satisfactory consistency.
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  • 119
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    Biopolymers 10 (1971), S. 2625-2628 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 120
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    Biopolymers 10 (1971), S. 2645-2648 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 121
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 85-114 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the small-angle scattering power and the degree of crystallinity in melt-crystallized high-density polyethylene have been used to evaluate the “amorphous” density in situ by the relation, \documentclass{article}\pagestyle{empty}\begin{document}$ (2\pi/V)\int_0^\infty {S\tilde g} (S)dS = (\rho_{\rm c} - \rho_{\rm a})^2 \upsilon_{{\rm er}} (1 - \upsilon_{{\rm er}}) $\end{document} where V is the irradiated volume and ḡ(S) is the “slit-smeared” absolute intensity. The amorphous density is a function of sample history and is always higher than the extrapolated melt density. After slit-height correction, and within the experimental error, the ratio of the two observed long periods is 2:1 at all temperatures (25--126°C). The lamellar thickness and the average interlamellar spacing are obtained from the degree of crystallinity and the first corrected long period. At increasing temperatures between 25°C and 110°C, the lamellae become thinner while the interlamellar zone expands by almost half. Over this range the changes are reversible with temperature. Above 110°C, both the lamellae and the interlamellar region expand with temperature. The thickening is partially reversible upon recooling. Other results obtained include measurements of stacking disorder and of microstructural changes with crystallization temperature and with time at ambient temperature.
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  • 122
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 143-160 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Work on two sheet organosilicon polymers, one derived from the mineral chrysotile and the other from the mineral apophyllite, is described. This work provides direct evidence that both these polymers are composed of sheets. In addition, it shows that in the chrysotile-derived polymer the sheets curl into scrolls, and that in the apophyllite-derived polymer the sheets are essentially flat.
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  • 123
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 209-243 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The shear creep and creep recovery behavior of narrow molecular weight distribution polystyrene samples of low molecular weight, 1.1 × 103, 3.4 × 103, and 1.57 × 104 are reported as a function of temperature, near and above the glass temperature. Time-temperature equivalence for the total creep compliance is found to be nonapplicable, and in fact the steady-state recoverable compliance, Je, is a strong function of temperature. The time-scale shift factors for the recoverable compliance are analyzed in the light of free volume theory. Viscosity data are presented for samples with molecular weights between 1.1 × 103 and 6.0 × 105. The temperature dependence of the characteristic time constant ηJe can be explained in terms of free volume concepts whereas that of viscosity η cannot. Effects of residual molecular weight heterogeneity are demonstrated.
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  • 124
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 295-311 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical calculation of the Hv light-scattering patterns for deformed three-dimensional spherulites is presented. Affine deformation is assumed. The optic axis of the scattering element is allowed to lie at an arbitrary angle ß to the radius which is permitted to change in the course of the deformation in a manner that may depend upon the angular location in the spherulite. The consequences of twisting of the optic axis about the spherulite radius are also explored.
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  • 125
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 331-343 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption of polydimethylsiloxane polymers from solution on glass has been studied. The amount of polymer adsorbed depends markedly on the solvent because of specific solvent - surface interactions. The presence of silanol groups in the polymer, particularly as endgroups, markedly increases the amount of polymer adsorbed. Large differences are shown between the adsorption of the commercially available, and fully trimethylsilylated polydimethylsiloxanes of narrow molecular weight distribut on. Possible adsorption mechanisms are discussed.
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  • 126
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 383-384 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 127
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 421-430 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A method is given for the analysis of long-chain branching in polymers by using combined GPC and intrinsic viscosity measurements. A computer program was written to evaluate branching indices by a tabular, iterative method. The method was applied to the evaluation of long-chain branching in low-density polyethylene.
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  • 128
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 431-435 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of stereoregularity on the low-temperature relaxation processes were studied by dynamic mechanical measurements on isotactic and syndiotactic polyisobutyl methacrylates (iso-PiBMA and syn-PiBMA). The α, β, and γ relaxation processes were observed in both stereoregular forms. Both the α, and β loss peaks were at lower temperatures for iso-PiBMA than for syn-PiBMA. The γ loss peak was observed at about -155°C at 30 Hz for both forms, and the apparent activation energy of this process was same for both samples within experimental error (6.7 ± 0.5 kcal/mole). It was reduced from these results that the α and β processes are both considerably influenced by the isotactic configuration but the γ process is not.
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  • 129
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    Journal of Polymer Science: Macromolecular Reviews 5 (1971), S. 385-430 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science: Macromolecular Reviews 5 (1971), S. 431-540 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 15-26 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gelation reaction of acetoguanamine with formaldehyde was investigated in the light of the gelation theory for tetrafunctional amino resins described in the previous paper. The gel time and extents of reaction of formaldehyde, amino groups, and imino groups varied with the molar ratio in the feed, but values of K (the ratio of the rate constant for condensation to that for addition) and k (the ratio of the rate constant for addition of the imino group to that of the amino group) were nearly constant. When the catalyst concentration was increased, the gel time, extents of reaction of each functional group, and the values of K and k varied; in particular K increased markedly. From the results of varying the molar ratio and concentration of acidic catalyst, it was found that the number of methylol groups per molecule of acetoguanamine at the gel point was influenced by the reaction conditions but the number of methylene linkages per molecular of acetoguanamine was nearly constant at about 0.6, regardless of reaction conditions. The number-average molecular weights up to the gel point varied with the reaction conditions, but at the gel point they were all nearly constant at about 385.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 543-555 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Photocurrents developed in polyethylene in the wavelength range 360-180 nm have been measured. The action spectra show features which can be related to the corresponding features in the absorption spectrum, and in addition there is electron injection from the metal electrode at a wavelength determined by the electrode material. The time dependence of the response indicates that a long-lived space charge is formed in the material.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 569-576 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10-5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 577-584 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was previously shown that for a stationary random copolymer of A, B, and C, we have in general p(AB) + p(AC) = p(BA) + p(CA), etc., in place of p(AB) = p(BA) which is valid for a stationary binary copolymer. Here, p(AB) for example, is the probability that a randomly picked pair of consecutive comonomers in the polymer consists of an A followed by a B. For a stationary ternary copolymer produced by a first-order Markovian addition mechanism, we show that PABPBCPCA/PACPCBPBA = k, where k is a constant characteristic of a particular set of three monomers but independent of its composition. Here, PAB is the conditional probability of finding a monomer of B given that its immediate predecessor is an A. We further show that if the individual rate constants of the monomer additions involved take a special form such as used in the Alfrey-Price Q-e scheme, then we have k = 1 irrespective of the kinds of monomers, and in addition we have p(AB) = p(BA), p(AC) = p(CA), etc. Thus, although these latter results were previously proposed by Ham as an alternative basis to supplant the Q-e scheme, they may rather be regarded as mathematical consequences of special assumptions adopted for the form of the individual rate constants. For a stationary random copolymer of four components A, B, C, and D, we have p(AB) + p(AC) + p(AD) = p(BA) + p(CA) + p(DA), etc., in general. For a first-order Markovian four-component copolymer, we show that there are seven different combinations of the conditional probabilities that are constants (k1, k2,…, k1) independent of the monomer composition. Again, if we assume the same special form for the rate constants involved, we find that all the seven constants k1, k2, …, k7 reduce to unity and p(XY) = p(YX) for X,Y, = A, B, C, D.
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    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 717-729 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several copolymers as well as homopolymers of vinylidene chloride and vinyl chloride have been examined by Raman spectroscopy. Probabilities of concentrations of monomer sequences have been calculated from known reactivity ratios. Surface scattering intensities at some frequencies were found to be linearly proportional to specific microstructure concentrations. Normalization of scattering intensities was accomplished using the intensity of the CH2 asymmetric stretching mode at 2926 cm-1, which is common to all samples examined. Good correlation was found for the concentrations of comonomer sequences {B}, {BB}, {BBB}, {AA} and {AAAA} in which A denotes vinylidene chloride and B vinyl chloride.
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    Journal of Applied Polymer Science 15 (1971), S. 247-250 
    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
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    Journal of Applied Polymer Science 15 (1971), S. 327-339 
    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 permeabilities of polyethylene film to vapors of 19 organic compounds at temperatures of 21°C, 38°C, and 49°C were measured by a sorption method. The film was formed into a pouch, which was filled with silica gel, sealed, and suspended in a saturated atmosphere. The permeability was calculated from the steady-state rate of the gain in weight. The permeability data were correlated with the Hildebrand solubility parameters of the organic substances.
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    Journal of Applied Polymer Science 15 (1971), S. 369-379 
    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 creeping flow of a highly viscous incompressible fluid through a circular aperture located in an infinitely wide horizontal plate is analyzed by solving Navier-Stokes equations without inertia terms. Solutions for vertical and radial velocities as well as pressure have been obtained in terms of integral equations with an undetermined Kernal function. This function has been evaluated by assuming several different velocity distributions at the aperture, and the corresponding pressure drop for each case has been calculated. The results show that the pressure loss for a given flow rate goes through a minimum as the assumed velocity profile changes from flat to parabolic. Based on the minimum energy dissipation theorem of Helmholtz, the most appropriate velocity distribution is discussed. Experimental data obtained using sharp-edged orifices are compared with theoretical predictions.
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    Journal of Applied Polymer Science 15 (1971), S. 597-606 
    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: Eastman cellulose acetate membranes (acetyl content = 40%) have been studied by means of dialysis rate experiments with uncharged permeants of selected sizes and shapes. The experimental results show that the high flux membranes exert no molecular size or shape selectivity on the transport of permeants whose molecular weights are less than 1152. The membranes used in desalination, however, are selective as to molecular size and shape. Desalination membranes, therefore, may be useful in separations where differences in size and shape are present.
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    Journal of Applied Polymer Science 15 (1971), S. 641-659 
    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 toughness and stress corrosion cracking characteristics of an epoxy resin (DER 332) hardened with hexahydrophthalic anhydride (HHPA) were investigated. The epoxy was studied in both the bulk and bond form, and its properties were compared with an amine-hardened (tetraethylene pentamine, TEPA) system. The toughness, GIc, of the anhydride system varied less as a function of ratio of hardener-to-resin content and postcure temperature than it did in the TEPA-hardened system. Like the latter, however, its toughness in the bulk and bond forms could not be correlated, but GIc of the joints was dependent on tensile modulus and/or yield strength of the bulk epoxy. Both systems were also toughened in the vicinity of the crack tip by water for short-time loading, but their long-time load carrying capability was reduced by a water environment. The anhydride hardened system was more sensitive to strength loss in water than the amine system. The fracture morphology for the two systems was the same, i.e., fast cracking occurred cohesively near the center of the bond, and slow cracking occurred at the interface.
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    Journal of Applied Polymer Science 15 (1971), S. 715-729 
    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 thermal decomposition behavior of rayon yarn which had been treated with various chlorosilanes and boron-phosphorus compounds was determined at temperatures up to 800°C. It was found that 70% of the available hydroxyl groups in rayon would react with dichlorodiphenylsilane and that the treated yarn had an initial decomposition temperature 125°C higher than that of untreated rayon. The weight loss of the treated yarn at 800°C was dependent on the nature of the chlorosilane and the type of posttreatment used. Alkylchlorosilanes produced higher weight losses than did the arylchlorosilane-treated rayons. Treatment of rayon yarn with bis(chlorodiphenyl-phosphine)decaborane (BCDPD) or dimeric chlorophospha(III)-o-carborane (DCPC) resulted in an increase in the char yield of the pyrolyzed yarns. In the case of untreated rayon, weight retention at 800°C was 20%, whereas the treated yarns yielded boronated residues of 42-53%. Carbon yields as high as 28% were obtained with the BCDPD treatment. This treatment also resulted in substantial improvement in the oxidative stability of rayon at temperatures up to 250°C.
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    Journal of Applied Polymer Science 15 (1971), S. 747-758 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The effect of N-methyl dithiocarbamate substitution on the radiation stability of poly-(vinyl chloride) (PVC) films was studied. PVC containing between 2 and 11 mole-% N-methyl dithiocarbamate (PMD) was irradiated with γ-rays from a 60Co source at 40°C and the evolved gaseous products were measured and analyzed with a mass spectrometer. The apparent G values for gas evolution for PMD decreased remarkably. For example, a G value of 0.28 was obtained for a PMD which contains 11 mole-% dithiocarbamate group compared with a G value of 10.8 for unmodified poly(vinyl chloride). Furthermore, the mass spectrum of the evolved gas from the same PMD sample (PMD-44) with 10 Mrad irradiation showed no hydrogen chloride to be present. The external protection was studied using polymer-blended films of PVC and PMD-44. The stabilization coefficients for internal protection and external protection in polymer blends were calculated. The ESR spectrum of the irradiated PMD-44 showed a strong anisotropy with high g values which differed significantly from the spectrum of the irradiated PVC. A suggested mechanism for radiation protection of PVC against γ-rays irradiation by the N-methyl dithiocarbamate group is discussed.
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    Journal of Applied Polymer Science 15 (1971), S. 811-828 
    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: An attempt has been made to rationalize the variables in the preparation procedure of Loeb-Sourirajan-type reverse-osmosis membranes. The quaternary phase diagram of the system cellulose acetate-acetone-formamide-water was determined and has proved a useful tool in the discussion of membrane structures and properties. A mechanism based on differences in the precipitation rate of the polymer during the membrane formation process has been suggested to explain the observed asymmetry in the membrane structure. The porosity of the membrane has been ascribed to the relative rates of water entering and solvent leaving the cast film. The effects of the casting solution composition, the evaporation time, the wash bath temperature, and the annealing procedure have been studied. X-Ray diffraction and electron microscopy were used to supplement flux and retention data of membranes made from a cellulose acetate-formamide-acetone casting solution.
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    Journal of Applied Polymer Science 15 (1971), S. 889-912 
    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: Large sublimed leaflets of titanium trichloride have been observed over a wide range of magnification both by optical and electron microscopy under conditions such that ethylene polymerization was slow enough so that its progress could be observed in detail. After treatment with triethylaluminum, a network of cracks develops on which polymer grows upon introducing ethylene. Polymer also appears on steps, crushed areas, and cleaved edges but not on as-grown edges. The polymer appearing on lateral surfaces was nodular in character while that growing on basal surfaces was fibrous. The physical properties of these two forms may be different, and methods for favoring one or the other are suggested.
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    Journal of Applied Polymer Science 15 (1971), S. 403-410 
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    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 inhibitory efficiences of antioxidants (phenols and aromatic amines) were determined under irradiation for elucidation of their behavior in photo-oxidation. We determined the ratio of termination rate constant to propagation rate constant and compared the ratio under irradiation with that in the dark. Phenols are classified into two categories with respect to their behavior under irradiation. The first is as antioxidants that have the same ratios under both conditions; the second, as antioxidants that have smaller ratios under irradiation than in the dark. We assumed the smaller ratios to be due to the following: quinones formed via the excited state of phenols by light absorption, in addition to the original phenols, participate in radical capture. Aromatic amines were also classified into two categories relative to their behavior under irradiation.
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    Journal of Applied Polymer Science 15 (1971), S. 419-435 
    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: Cellulose samples modified by iodination, benzhydrylation, and benzhydrylation followed by iodination were pyrolyzed to investigate the potential flame retardance of such treatments. Their effect on crystallinity, rate of thermal degradation, char production, and pyrolysis products was determined. Results indicate that in general the crystallinity index varies inversely with the percentage of substitution, rate of weight loss, and amount of residual char. Although the rates of weight loss of the substituted samples increased from 0.3%/min to 108%/min, depending on the type and percentage of substitution, the overall weight loss pattern of the treated cellulose was similar to that of the untreated samples. Of the three treatments, iodination appears to offer the best flame retardance in that the residual char is increased by a much larger factor for a given weight loss rate. On the other hand, addition of the benzhydryl to the iodinated sample decreases the char. All three treatments drastically reduce the number of degradation products of molecular weights lower than 150; untreated cellulose gave 59 components, whereas the substituted cellulose produced five major compounds: water, acetic acid, furfural, 5-methyl-2-furaldehyde, and 1,5-anhydro-2,3-deoxy-β-D-pent-2-eno-furanose. Of these, water and the furanose derivatives were the major components.
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    Journal of Applied Polymer Science 15 (1971), S. 1365-1375 
    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: If a low-density polyethylene sheet is treated in a corona discharge and subsequently pressed to a similarly treated sheet at 45°C, the bond formed is much stronger than that between similarly pressed but untreated sheets. Several series of observations have indicated that this enhanced autohesion is not due to surface oxidation or to surface crosslinking (CASING). Evidence is presented that the effect may be related to some type of electret formation induced in the polymer sheet by the corona discharge.
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    Journal of Applied Polymer Science 15 (1971), S. 1231-1235 
    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: In order to determine the effect of the molecular structure of short side branches in lowdensity polyethylene upon the physical properties of the resin, a study was carried out in which small amounts of various comonomers were added to an otherwise relatively unbranched polymer. It was found that linear short side branches have about the same effect in decreasing stiffness and increasing toughness as the natural short-chain branches of polyethylene have. However, branches containing a tert-butyl group increased resin toughness more than linear branches while decreasing stiffness by about the same amount. Thus, by adding a small amount of branched, short side branches, it is possible to obtain an optimum balance of physical properties not obtainable from low-density ethylene homopolymer.
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    Journal of Applied Polymer Science 15 (1971), S. 1479-1492 
    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 rapid iteration method has been developed to correct the molecular weight averages calculated from raw GPC data for dispersion. Though simple in its performance, it covers the general case that the instrumental spreading characteristics (Tung's resolution factor h) depend on the elution volume. Moreover, it is irrelevant whether the calibration curve, being the logarithmic plot of the molecular weight versus the elution volume, is linear or not. The method has been applied to a number of well-characterized polystyrene mixtures and yields molecular weight averages which agree with those predicted theoretically. The effect of asymmetry exerted by the dispersion on both molecular weight averages M̄n and M̄w is also discussed.
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    Journal of Applied Polymer Science 15 (1971), S. 1641-1648 
    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: By combining a number of theoretical relationships concerning the effect of molecular weight on melt rheology, an equation may be derived for conversion of melt indexer flow rate to “apparent molecular weight.” In spite of certain evident theoretical shortcomings of this derivation, the method was applied to the determination of the molecular weight of highly crystalline insoluble poly(ethylene sulfide), for which no other method appeared to be satisfactory. When applied to polymer specimens of presumably known molecular weight (e.g., certain ionically initiated specimens), reasonable agreement was found.
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    Journal of Applied Polymer Science 15 (1971), S. 1679-1685 
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    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: Using carbon blacks of constant specific surface area and surface chemical characteristics, but differing in degree of structure, it is shown that tensile strength, elongation at break and rupture energy are functions of the product av2, where v2 is the volume concentration of carbon black and a is a structure dependent factor. Moreover, reductions of failure data to a common effective filler concentration are accomplished with the identical structure factors used earlier in modulus reductions. The values of the structure factors are linearly related to the dibutyl phthalate (DBP) absorption of carbon black, when care is taken to equalize the packing density prior to conducting the DBP test.
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  • 152
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    Notes: The Gram-Charlier series was suggested as an empirical instrument spreading function in the first paper (part I) of this series. In the second paper (part II) of this series, the Fourier transform method was used together with the suggested series to solve Tung's integral equation. In this paper, an alternate method for solving Tung's equation is proposed which eliminates some of the limitations of the Fourier transform method. In the approach used in this study, Tung's integral equation is approximated by a set of linear equations. Since no unique least-squares solution can be computed, a closely related problem whose solution closely approximates the original problem is formulated and solved using singular value decomposition. By avoiding the use of the smallest singular values and forcing the equality of the areas of the corrected and the uncorrected chromatograms, an approximate solution to the original problem is obtained in which the oscillations inherently present due to the ill-posed nature of the problem are filtered out. The performance of the method with the experimental data given in Part II is indicated.
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    Journal of Applied Polymer Science 15 (1971), S. 1729-1736 
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    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 concentric cylinder conductivity cell with guard heaters was constructed and used to determine the thermal conductivity of polymer melts. Thermal conductivity was found to be a linear function of temperature for the melts studied, and the thermal conductivity decreased as the complexity of the polymer chain increased. The polymers studied were a linear polyethylene, branched polyethylene, polypropylene, polystyrene, nylon 6, and nylon 6,10. The measurements are precise to within ±6%.
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    Journal of Applied Polymer Science 15 (1971), S. 1753-1756 
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    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: In an earlier communication1 the preparation of Bisacid A2 was described. This paper describes the attempts at spotting impurities in the products so obtained by subjecting them to thin-layer chromatography. No traces of impurities could be detected since no separation whatever was observed. Infrared spectra of pure Bisacid A2 were found to be identical with the spectrum of Nanu and Boboescu.2 It was also seen that the product obtained by the standard preparation in 70-73% yield with a minimum melting point of 173°C could not be demonstrably improved by esterification and rehydrolysis. Second crops from first mother liquors from the aqueous acetic acid recrystallization of the crude precipitated product of the condensation reaction (as well as ether extracts from these mother liquors) showed that both contained material with phenolic OH groups. These are the inpurities in the crude product which must be completely removed during purification if the final material is to be used for the synthesis of unsaturated polyester resins for ultimate use as crosslinked reinforced plastics, as alkyd varnish bases, or as fiber-forming saturated polyesters and polyamides. The need for adhering to the standard synthetic procedure was confirmed, in particular the need for multistage condensation, giving an effective yield of 70-73% of pure material
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    Journal of Applied Polymer Science 15 (1971), S. 1649-1655 
    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 rheological behavior of the two-phase systems consisting of a polystyrene-in-styrene phase distributed in a rubber-in-styrene phase is shown to exhibit increasing non-Newtonian behavior up to the phase inversion point, as a consequence of its two phase nature. The equation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \frac{\mu }{{\mu _c }} = 2.5\left( {\frac{{\mu _d + a\mu _c }}{{\mu _d + \mu _c }}} \right)\left( {\phi + \phi ^{{\raise0.7ex\hbox{$5$} \!\mathord{\left/ {\vphantom {5 3}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$3$}}} + \phi ^{{\raise0.7ex\hbox{${11}$} \!\mathord{\left/ {\vphantom {{11} 3}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$3$}}} } \right) $$\end{document} is recommended for the prediction of the viscosity of the polymerizing mass up to phase inversion during the production of HIPS by the in situ bulk polymerization of styrene in the presence of dissolved rubber.
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  • 156
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    Journal of Applied Polymer Science 15 (1971), S. 1703-1708 
    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 simple, moderately high shear capillary viscometer which can be used up to a shear rate of 150,0000 sec-1 is described. The use of a twin viscometer arrangement has eliminated the need of elaborate pressure control and adjustment units. Experimental results obtained by use of the viscometer to measure the specific viscosities of a charged colloid at two different shear rates are presented.
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  • 157
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    Journal of Applied Polymer Science 15 (1971), S. 1665-1677 
    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: Membranes of graft copolymers of polyethylene with poly(sodium styrene sulfonate), poly(4-vinylpyridinium methyl bromide), and poly(sodium acrylate) were prepared by using the technique of peroxide grafting. The reverse osmosis characteristics of the membranes were examined as a function of grafting yield. In these membranes, the grafting can be considered as a process of introducing ionic sites, and it depends on the conditions of the grafting reaction, such as monomer concentration and temperature. However, the overall reverse osmosis characteristic is not only dependent on the number of ionic sites introduced but also on the swelling capability of the membrane. Consequently, the salt rejection of grafted membrane of a fixed graft yield depends on the conditions of the grafting reaction. All grafted membranes which have grafting yields above a certain value behave as normal ionic polymer membranes, and their interrelationship of salt rejection and water permeability follow the general dependence found for ionic polymer membranes.
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  • 158
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    Journal of Applied Polymer Science 15 (1971), S. 1709-1715 
    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: Axial stresses generated by polyacrylonitrile filaments heated in air at constant length and length changes of filaments heated at constant load were measured. Fibers subjected to loads less than about 0.1 gpd shrank in the temperature range from about 40°C to 160°C. At about 160°C they began to stretch. Fibers that stretched out again to about their original lengths stiffened temporarily before undergoing a further elongation. At a temperature where the oxidation reaction begins to proceed with appreciable rate, elongation was retarded and finally reversed. Shrinkage was recorded during isothermal heating at 270°C, and a final length was approached when the oxygen content approached about 10 wt-%. The tension generated when the fibers were restrained from shrinking increased as temperature increased to 160°C but dropped in the temperature range of 160° to 250°C. Tension again built up during isothermal oxidation at 270°C. In the case of one of the samples, the tension generated below 160°C exceeded the ultimate tensile strength of the fibers above 200°C. This condition leads to tensile failures when the filaments are heated in a steep thermal gradient. The tensile behavior of the filaments is discussed in terms of the helical molecular model.
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  • 159
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    Journal of Applied Polymer Science 15 (1971), S. 1717-1727 
    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 comparative thermogravimetric study of ten polyimide films of varying composition revealed that thermal and thermo-oxidative stability of the polymers increases directly with increasing imide content. Films degraded more rapidly in air than in vacuo; the insertion of connecting groups within the polymer repeat unit decreased stability in both environments. The effect of inserting “ladder-like” segments in the polymer structure did not enhance resistance to oxidation; but under vacuum, those segments probably operated beneficially in promoting the retention of the carbon-like residue. Infrared spectral measurements showed little loss of imide bands with progressive weight loss in air, indicating unit-by-unit degradation. Conversely, infrared spectra of films heated under vacuum conditions showed that progressive loss of imide bands occurred simultaneously with an increasing development of bands related to carbon-nitrogen double bonds. Dynamic heating under vacuum developed singularly uniform weight loss curves; however, concurrent mass-spectrographic analyses indicated two distinct reactions. Gaseous carbon monoxide and carbon dioxide species accounted for the major weight change, and their periods of maximum evolution occurred at different temperatures for each film. A subsequent minor weight loss period was associated with the liberation of hydrogen cyanide which maximized at the same temperature for all ten films.
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  • 160
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    Notes: The degree of branching of a series of ethylene-vinyl acetate copolymers was found to be strongly dependent upon polymerization temperature. The copolymers were prepared by free-radical polymerization and had low molecular weights and molar ratios of ethylene: vinyl acetate greater than 3:1. Nuclear magnetic resonance and infrared studies showed that copolymers prepared at 150°C were highly branched and had little crystallinity. Branches were mainly alkyl groups on the polymethylene backbone segments. There was no evidence of δ-acetoxyalkyl branches. Long branches originating by intermolecular H abstraction from the acetylmethyl groups were also expected but could not be detected. These results were consistent with an intramolecular “backbiting” mechanism similar to that found in ethylene homopolymerizations. There was little or no participation by the vinyl acetate moiety in the branching scheme. Copolymers prepared at about 90°C had very few long or short branches and were more crystalline. Copolymers prepared between these temperatures had intermediate degrees of branching and crystallinity.
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  • 161
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    Journal of Applied Polymer Science 15 (1971), S. 1769-1775 
    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: Measurements of solubility parameters of a series of chlorinated poly(vinyl chloride) (CPVC) samples were carried out. A maximum value of solubility parameter occurs at a chlorine content of 63-65% and is related to optimum packing.
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  • 162
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    Journal of Applied Polymer Science 15 (1971), S. 1791-1801 
    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 grafting reactions of styrene (St), methyl methacrylate (MMA), and vinyl acetate (VAc) were investigated in the presence of n-butyl acrylate-acrylonitrile copolymer. Results showed that the nature of monomer and initiator were the major factors influencing the grafting activity. The grafting efficiency was 0.87 for St, 0.26 for MMA, and 0.18 for VAc under the most favorable conditions. Acrylic rubber reduced the rate of polymerization, and the retarding effect increased in the order St, MMA, VAc. The chain transfer constants for acrylic rubber were evaluated to be 4.8 × 10-4 for St, 1.27 × 10-3 for MMA, and 1.45 × 10-3 for VAc. The rate of polymerization and the grafting efficiency decreased with increasing acrylonitrile content in acrylic rubber, while the chain transfer constant of St for acrylic rubber remained practically unchanged.
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  • 163
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    Journal of Applied Polymer Science 15 (1971), S. 1819-1835 
    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 change of the mixing state of polybutadiene rubber-polyolefin resin blend resulting from remilling and heat treatment was studied. Polyolfin resins studied here were high-pressure polyethylene, low-pressure polyethylene, and polypropylene. As in case of polybutadiene rubber-general purpose polystyrene resin blend, we made use of the results obtained through hardness and compression modulus measurement and microscopic observation. Even in case of polybutadiene rubber-polyolefin resin blend, the change of mixing state and the softening phenomenon by remilling were observed. The hardening phenomenon by heat treatment of the sample softened by remilling was also observed at high polyolefin resin content. But at low polyolefin resin content, the hardness which had increased once often decreased as the heat treating time increased, and in some cases the nonremilled sample was observed to soften with heat treatment. These phenomena attendant on heat treatment show that the intrinsic nature of a heterogeneous blend system also appears in a microheterogeneous polymer blend system.
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  • 164
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    Journal of Applied Polymer Science 15 (1971), S. 1855-1868 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: A comparison is made of the composition and properties of the different rubber vulcanizate networks obtained by varying the ratio of sulfur to sulfenamide accelerator and by the thermal aging of vulcanizates containing predominantly polysulfide crosslinks. It is concluded that the changes in network structure which can take place, for example, during the service life of natural rubber tires are not the direct cause of failures of the type associated with rubber fatigue at high temperatures. However, a reduction in the total number of crosslinks can accelerate failure by increasing the amount of heat generated during flexing. More stable networks giving improved resistance to fatigue at high operating temperatures are obtained by the use of higher ratios of accelerator to sulfur than are conventionally employed.
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  • 165
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    Journal of Applied Polymer Science 15 (1971), S. 1903-1909 
    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 continuum modification of the bead-spring (elastic dumbbell) theory of dilute solutions of linear macromolecules, recently introduced by Gordon and Schowalter, is used to obtain explicit constitutive equations for the stress and polarizability tensors. The stress constitutive equation, closely related to a semiempirical result obtained earlier by Spriggs, is superior in predictive capability to the constitutive equation obtained from the elastic dumbbell theory. Results are presented for steady shearing flow, large-amplitude oscillatory shearing, and stress relaxation following cessation of steady shearing and are compared with the results of the elastic and rigid dumbbell theories. In general, predictions are similar to those of the rigid dumbbell and thus are in qualitative agreement with experiment.
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  • 166
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    Journal of Applied Polymer Science 15 (1971), S. 1941-1948 
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    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 failure criterion developed by Harwood et al. between energy input to break and hysteresis at break for amorphous rubbers has been related to the fatigue and cut growth properties of the rubber which are based on the tearing energy theory. It is found that the constant K in the hysteresis failure criterion is a function of the cut growth constant G and the inherent flaw size C0. The effect of adding fine particulate fillers to amorphous rubbers on the hysteresis and fatigue properties is considered and shown to be in agreement with the theory.
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  • 167
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    Journal of Applied Polymer Science 15 (1971), S. 2317-2319 
    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
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    Journal of Applied Polymer Science 15 (1971), S. 2321-2333 
    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 computer technique ultimately yielding, from GPC data, both differential and integral molecular weight distributions of macromolecular products with unknown composition and structure has been worked out, based on a “universal” calibration method previously proposed by other authors to calculate average molecular weights. The technique involves as sole assumption the validity of the “universal” calibration for the kind of sample under investigation. The GPC output data are handled through a realtime computer program and punched on paper tape. Together with two experimental parameters of the polymer (average molecular weights, limiting flow number) and the “universal” calibration of the columns set, the tape is used as input for the off-line programming. Examples are presented, showing the accuracy which can be expected.
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  • 169
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    Journal of Applied Polymer Science 15 (1971), S. 2371-2380 
    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 intermolecular cyclization reaction is investigated in highly crosslinked epoxy systems, where diepoxides with different mobilities between terminal epoxy groups were crosslinked with ethylene diamine. Based on the measured values of the Clash-Berg 10-sec modulus in the rubbery region, the correlation between the mobility and the cyclization reactivity of the diepoxides is discussed. The epoxide with higher mobility is found to have a higher rubbery modulus than that with lower mobility, as was expected. This is tentatively explained by the difference in the reactivity of the formation of the 11-membered ring. Dynamic mechanical measurements were also run on a forced vibration apparatus. The higher β-transition peak of the polymer of bisphenol-A diglycidyl ether was interpreted in terms of its higher free volume as well as lower density and lower glassy modulus. The higher modulus in the glassy region of ethylene glycol diglycidyl ether-ethylenediamine was explained on the basis of hydrogen bonding.
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  • 170
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    Journal of Applied Polymer Science 15 (1971), S. 2417-2424 
    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 catalyst comprised of triisobutylaluminum, zinc acetylacetonate, and water was used to prepare homopolymer of epichlorohydrin; copolymers of epichlorohydrin with propylene oxide, ethylene oxide, and allyl glycidyl ether; and terpolymers of epichlorohydrin, propylene oxide, and allyl glycidyl ether and of epichlorohydrin, ethylene oxide, and allyl glycidyl ether. The vulcanizates of these rubbers provide variations of stressstrain and dynamic properties, freeze point, hardness, and solvent resistance depending on the type and amount of comonomer. In general, these rubbers have excellent heat, ozone, and oxidation resistance as well as oil and solvent resistance.
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    Journal of Applied Polymer Science 15 (1971), S. 2453-2460 
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    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: At lower than the glass transition temperature, the cleavage of the molecular chains of extended vulcanized rubbers will occur. The crosslinking density of vulcanized rubbers, which were placed at room temperature for about 4 hr in nitrogen atmosphere, increased about 17% after extension of 200% at -76°C. This may be due to the recombination of cleft chains, and this can be shown by the Maxwellian type of curves between crosslinking density and forced strain. Considering the decreasing proportion of crosslinking density by the radical acceptors included in the rubbers and the fact that crosslinking density increases because of recombination of cleft chains, this was attributed to the recombination of unstable chains produced by the added mechanical stimulus.
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  • 172
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    Journal of Applied Polymer Science 15 (1971), S. 2103-2114 
    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: Terpolymers of ethylene and propylene with 4-phenyl-, 4-o-tolyl, 4-p-tolyl, and 4-(1-naphthyl)-1-butenes were vulcanized with bisbenzylic halides in the presence of highly acidic clays. The halides include bischloromethyldurene, p-bischloromethylbenzene, and p-bisbromomethylbenzene. Since the polymers contain no olefinic unsaturation, the crosslinking is achieved by electrophilic attack of the halide on the pendant aromatic rings. The order of activity is naphthyl 〉 tolyl 〉 phenyl. The new curing system also reacts with olefinic unsaturation. Thus, an EPDM elastomer and SBR rubber, the latter containing both aromatic rings and double bonds, were also readily crosslinked.
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  • 173
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    Journal of Applied Polymer Science 15 (1971), S. 2123-2140 
    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 ultraviolet stability of polyimides and polyamide-imides was determined in both a wet and dry environment. Films have been exposed to these environments for 3000 and 6000 hr, respectively. The polymers are not stable to UV radiation (2900-4000 Å); serious deterioration of the mechanical properties occurs under both wet and dry conditions with the former giving rise to greater damage. The polyamide-imide polymer is more unstable to UV radiation than the two polyimides evaluated; however, it is more resistant to hydrolysis as indicated from rate data obtained from a kinetic analysis of the mechanical property degradation curves. The electrical properties of the polymers are relatively unaffected in the dry environment but begin to deteriorate as the polymer becomes brittle. In the wet environment these properties begin to deteriorate more rapidly. Dissipation factor and dielectric strength are the properties most affected.
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    Journal of Applied Polymer Science 15 (1971), S. 2199-2210 
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    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 pressure-driven transport of liquids employed in reverse osmosis has been shown to occur by a solution-diffusion mechanism in highly swollen polymer membranes. A theory based on this mechanism was successfully used earlier to correlate permeation fluxes for such membranes. Positive confirmation of this theory is provided here by direct measurement of the proposed concentration gradient. A study of the temperature dependence of the liquid diffusion coefficient in the polymer membrane has provided additional evidence of a hydrodynamic regime of diffusion in highly swollen membranes. It is also shown that the proposed ceiling flux in reverse osmosis is equal to the pervaporation flux.
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  • 175
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    Journal of Applied Polymer Science 15 (1971), S. 2219-2236 
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    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: Diene polymers (i.e., polyisoprene, polybutadiene, and butadiene - styrene copolymers) were hydroxylated in tetrahydrofuran by hydroboration with diborane and subsequent alkaline oxidative hydrolysis. The strong, broad infrared absorption of the product at 3340 cm-1 shows the introduction of hydroxyl group. The properties of hydroxylated diene polymers depend upon the extent of hydroxylation. The less hydroxylated polymers are rubbery. As the extent of hydroxylation increases, the product becomes a white thermoplastic which is soluble in alcohol. The hydroboration of diene polymers with diborane is very rapid. However, if the reaction is continued further, the extent of hydroxylation decreases because of side reactions. The results of acetylation and formylation of the hydroxylated products and the grafting of vinyl monomers onto hydroborated diene polymers are also presented.
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    Journal of Applied Polymer Science 15 (1971), S. 2567-2577 
    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: Two slit dies have been designed, having aspect ratios of 10 and 20. Three melt pressure transducers were flush-mounted on the long side of the rectangular slot, along the longitudinal centerline of each die. The dies were then used to measure wall normal stresses along the longitudinal direction of polymer melts flowing through the thin slit. The polymeric materials investigated were high-density polyethylene, low-density polyethylene, polypropylene, and polystyrene. The measurement of wall normal stresses were used to determine the rheological properties of melts, namely, the melt viscosity from the slope of axial pressure profiles and the melt elasticity from exit pressures. The present study shows that the rheological properties determined from the slit rheometer are in good agreement with those from the capillary rheometer reported in the author's earlier papers. Therefore it may be concluded that a slit die also may be used as a means of characterizing polymeric materials by their viscous and elastic properties in the molten state.
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    Journal of Applied Polymer Science 15 (1971), S. 2597-2599 
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    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
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    Notes: The hydrochloride salt of 1,1-dimethyl-1-(2-hydroxypropyl)amine methacrylimide (DHA) was synthesized and shown to readily homo- and copolymerize with styrene to produce soluble polymers containing pendent quaternary ammonium groups. These polymers may be treated with base to provide modified polystyrenes containing pendent aminimide residues. The latter polymers may be thermolyzed in solution or in the solid phase to produce modified polystyrenes containing pendent isocyanate groups. If the thermolysis is carried out in the presence of “isocyanate reactive” moieties, high molecular weight, crosslinked polymers may be synthesized. The reactivity ratios of DHA · HCl with styrene were determined: r1 = 0.33 and r2 = 0.35. The Alfrey-Price Q and e values were also calculated: Q = 0.88 and e = 0.67.
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  • 179
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    Notes: Seven monomers, which varied widely in water solubility and ionic charge, were graft polymerized onto both unswollen starch and starch that had been swollen by heating in water to 60°C. Polymerizations were initiated with ferrous ammonium sulfate hexahydrate-hydrogen peroxide and, where applicable, with ceric ammonium nitrate. Graft copolymers were freed of ungrafted homopolymer by solvent extraction and were characterized by weight percentage of synthetic polymer incorporated in the graft copolymer, molecular weight of grafted branches, and grafting frequency. The influence of starch granule swelling on graft copolymer structure varied with the monomer used and could not be predicted on the basis of water solubility of monomer or its resulting polymer. With acrylonitrile and acrylamide, swollen starch gave higher molecular weight and less frequent grafts than unswollen starch. However, methyl methacrylate, N,N-dimethylaminoethyl methacrylate · HNO3, N-t-butylaminoethyl methacrylate. HNO3, and 2-hydroxy-3-methacryloyloxypropyltrimethylammonium chloride produced less frequent graft of higher molecular weight when starch was unswollen. With acrylic acid, graft molecular weight was independent of starch granule swelling, although grafting was less frequent when swollen starch was used.
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    Journal of Applied Polymer Science 15 (1971), S. 2687-2697 
    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: Investigations of glass transition phenomena were carried out on vinylidene chloride - acrylonitrile copolymers, purified commercial samples of known composition. With a view to analyzing this effect, the following physical parameters were investigated: specific volume Vs,25, Tg, and volume expansion coefficients αL, αg, and Δα. The experimental results were analyzed on the basis of semiempirical and theoretical equations describing transitions to the glassy state. It was found that Tg dependence on weight fraction C2 of acrylonitrile may be described by Wood's equation, with k = 5.88. Applying Gibb's and Kanig's theories as well as relations given by Hirai and Small, the energies associated with intermolecular interactions (A*AB, E0, Eh, CED), and intramolecular interactions (stiffness energy ε) were calculated for copolymers of different composition. The copolymer Tg was found, above all, to depend on the stiffness energy ε, which increases with increasing acrylonitrile content in the copolymer.
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    Journal of Applied Polymer Science 15 (1971), S. 2277-2292 
    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 polymerization (polymer deposition) rate of styrene in an electrodeless glow discharge from styrene vapor and a mixture of styrene vapor and gas (H2, He, A, and N2) was investigated. The rate of polymerization, R, was found to be independent of the discharge power. The rate of polymerization of the pure monomer was found to be proportional to the square of monomer pressure pM. The addition of gas increased the rate of polymerization depending upon the partial pressure of the gas, px, and R can be generally expressed by R = a[pM]2{1 + b[px]}. The value of b is dependent of the type of gas and follows the order of N2, 〉 A 〉 He 〉 H2. The distribution of polymer deposition was found to be nearly independent of the partial pressure of the gas and of the discharge power with N2 and H2 as plasma gas; however, with He and A, the distribution is highly dependent on the partial pressure of the gas and on the discharge power. The study strongly suggests that polymerization occurs in the vapor phase and that the growing polymer radicals deposit on the surface of the discharge vessel, yielding highly crosslinked polymer deposition.
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    Journal of Applied Polymer Science 15 (1971), S. 2303-2315 
    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 mechanical behavior of three kinds of organic foams, each at two different densities, was experimentally investigated under conditions of pulsed one-dimensional strain shock loading. The input pulse width in each experiment was nominally 0.1 μsec, and the input stress level (as referenced to quartz) was varied between 10 and 23 kbar. The materials studied were polyurethane foam at bulk densities of 0.33 and 0.21 g/cc, syntactic foam (phenolic microballoons dispersed in a resin binder) at 0.66 and 0.23 g/cc, and polystyrene bead foam at 0.091 and 0.049 g/cc. Specimen thicknesses varied between 1.0 and 6.5 mm. It was found that the pulse duration was greatly lengthened and that the peak stress was decreased (accounting for both impedance mismatch and attenuation effects) by factors of between about 8 and 500, depending upon the type of foam, its thickness, and its density.
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    Journal of Applied Polymer Science 15 (1971), S. 2357-2369 
    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: Using the Weissenberg rheogoniometer, a technique has been developed which facilitates the measurement of shear stress data and which substantially overcomes the problem of sample loss that normally occurs at high shear rates. Using this technique, the apparent viscosities of PVC pastes based upon four different PVC paste polymers plasticized with dialphyl phthalate have been determined at a number of shear rates up to 9000 sec-1 and the viscosity aging characteristics of these paste polymers have been compared. The effect of several common plasticizers upon PVC paste viscosity and viscosity aging have been studied at shear rates of the order of 10 sec-1 and 1000 sec-1.
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    Journal of Applied Polymer Science 15 (1971), S. 2645-2650 
    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 new synthesis for carboranesiloxane polymers has been discovered. It involves the alcoholysis of the bischlorodimethylsilylcarborane monomers and the generation of the HCl catalyst in situ. Alcoholysis is applicable to the synthesis of most carborane-siloxane polymers, with the probable exception of the SiB-1 homopolymers of the larger carboranes. The attack of the B—H moieties in the carborane cage can be minimized both by the utilization of a tertiary alcohol and by the addition of excess acid when a primary alcohol is employed.
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  • 185
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    Journal of Applied Polymer Science 15 (1971), S. 2439-2445 
    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: Criteria for establishing a universal GPC calibration for poly-1,2-butadiene on the basis of polystyrene standards are considered. The number-average molecular weights of the two polymers are related by a linear expression on the assumption that their respective Mark-Houwink exponents are equal. The coefficient Cn of this expression, determined from GPC and viscosity measurements, remained constant for a considerable range of molecular weights and polydispersities. The applicability of Cn beyond the interval of present measurements is considered on the basis of results in the literature. The results are comparable to those obtained from a universal calibration based on the unperturbed dimension of polymer chains, but do not agree with those obtained from a model based on extended length.
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  • 186
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    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 temperature dependence of the shear modulus G′ and of the damping tan δ of poly-(vinyl chloride), poly(vinylidene chloride), copolymers of vinyl chloride-vinylidene chloride, PVC chlorinated in solution and suspension, and chlorinated polyethylene was measured. Secondary relaxation process of PVC and its derivatives are being explained as vibration of methylene groups polarized by neighboring CCl dipoles. This process, being suppressed by lowering the concentration of the methylene groups in the PVC chain (e.g., by chlorination), remains, however, unaffected by the growth of crystalline content. The achieved results show that in the α-transition region there occurs, in accordance with Andrews' theory, a loosening of the bonds between the CCl dipoles, whereas in the β-transition region a loosening of the weaker bonds among the dipoles of the polarized methylene.
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    Journal of Applied Polymer Science 15 (1971), S. 3109-3116 
    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: Nylon fibers tested in tension at -196°C show ductile strains up to 75%. The ductility is a complicated function of draw ratio, because decreasing work hardening with decreasing draw ratio leads to a point of instability where necking begins. The necks presumably initiate fracture, have the appearnce of cracks, and have been previously seen on fibers drawn in various organic liquids. Recovery experiments showed that molecular motions involved in low temperature deformation differ from those involved in ambient temperature deformation.
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 112-112 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 123-127 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Creep and Creep-Rupture Behaviour of Materials- and the Fundamentals of High Temperature Plasticity. Principles of evaluation methods for creep data (strain vs. time) for technological purposes as well as in fundamental research. Derivation and discussion of equations representing rupture-life and constant strain curves in creep rupture diagrams. Consequences for extrapolation of short-time tests.
    Notes: Prinzipien der Auswerte-Methodik für Kriechmeßdaten (Dehnung als Funktion der Zeit) bei technischer und bei wissenschaftlicher Zielsetzung. Ableitung und Diskussion von Gleichungen für Zeitbruch- und Dehngrenzlinien im Zeitstandschaubild. Konsequenzen für die Extrapolation von Kurzzeittests.
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 127-135 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Thermal aging and endurance of organic insulating materials. The knowledge of the thermal endurance of organic insulating materials is very important for the application in electrical engineering. The change of the values of the properties by thermal aging is, theoretically, described under the assumption being a linear connection to the rules of the kinetic theory of chemical reactions. By this premise it is possible to indicate functions for aging and thermal endurance, being plotted as straight lines in suitable coordinates. In this way the test results can be evaluated better than by conventional means.
    Notes: Die Kenntnis der Grenztemperatur organischer Isolierstoffe ist für deren Anwendung in der Elektrotechnik von großer Wichtigkeit. Die Änderung von Eigenschaftswerten auf Grund einer Wärmebehandlung wird theoretisch beschrieben unter der Annahme, daß ein linearer Zusammenhang mit den Gesetzen der Reaktionskinetik besteht. Unter den getroffenen Voraussetzungen können. Alterungs- und Lebensdauerfunktionen angegeben werden, die sich bei geeigenten Koordinaten als Geradendarstellen lassen. Meßergebnisse können auf diese Weise besser ausgewertet werden als nach herkömmlichen Verfahren.
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  • 191
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 135-144 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Analytical Chemistry used for developing new materials. The development of new materials constantly confronts the analyst with difficult new problems. Of particular importance for this work would be all methods permitting to lay bare the phase interface and to study their structure and perturbations of this structure. The analyst has to solve these problems in close contact with the technologists specializing in this modern technique.
    Notes: Die Entwicklung neuer Werkstoffe stellt den Analytiker vor immer neue diffizile Aufgaben. Insbesondere dürften alle Verfahren, mit denen es gelingt, Phasengrenzflächen freizulegen und ihren Aufbau sowie Störungen in diesem Aufbau zu studieren, für diese Aufgaben von großer Bedeutung sein. Der Analytiker muß diese Aufgaben in engster Fühlung mit den Technologen, die sich dieser modernen Entwicklung verschrieben haben, lösen.
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  • 192
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 113-123 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Cold-Rolled Flat Products of Plain Carbon Mild Steel According to DIN 1623 Sheet 1. Cold-rolled flat products of plain carbon mild steel and among the most important finished products made by iron and steel works and rolling mills as well as being among the most important semi-products for industrial manufacture. Metallurgical and rolling developments during the course of the last twenty years have resulted in considerable improvements in the main cold forming properties of sheet and strip. The chief demand made of manufacturers of cold-rolled flat products is for sheet and strip which has been fully annealed and rerolled for good cold formability. Because of the various stresses on materials in the different forming processes, it is difficult to make a reliable prediction from test results about the behaviour of the material during actual forming operations. The new edition of sheet 1 of DIN 1623 prescribes the conventional test methods and their results as regards ensuring cold formability. The Standard does not include the additional means of using numerical values for vertical anisotropy r, work hardening exponent n and the maximum drawing ratio (ßo)max.
    Notes: Kaltgewalztes Flachzeug aus unlegierten weichen Stählen ist eines der wichtigsten Walzwerksfertigerzeugnisse der Hütten- und Walzwerke und ebenso eines der wichtigsten Halbzeuge für die industrielle Fertigung. Die metallurgische und walztechnische Entwicklung haben vor allem im Verlauf der beiden vergangenen Jahrzehnte zu bedeutsamen Fortschritten hinsichtlich der für die Kaltumformung der Bleche und Bänder wichtigen Eigenschaften geführt. Die wichtigste Forderung der Verarbeiter kaltgewalzten Flachzeugs ist die nach bester Kaltumformbarkeit der rekristallisierend geglühten und nachgewalzten Bleche und Bänder. Dabei ist es wegen der unterschiedlichen Werkstoffbeanspruchung bei den einzelnen Umformungsprozessen schwierig, mit Hilfe von Prüfergebnissen eine zuverlässige Vorhersage des Werkstoffverhaltens bei der betrieblichen Umformung zu machen. Die Neufassung des Blattes 1 der DIN 1623 legt hinsichtlich der Gewährleistung der Kaltumformbarkeit die konventionellen Prüfverfahren und deren Ergebnisse zugrunde. Eine zusätzliche Bewertung unter Verwendung der Zahlenwerte für die senkrechte Anisotropie r, den Verfestigungsexponenten n und das Grenzziehverhältnis (ßo)max ist zur Zeit im Rahmen der Norm nicht angebracht.
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 150-154 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 156-159 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 224-224 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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    Materialwissenschaft und Werkstofftechnik 2 (1971) 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 232-242 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: The formation of austenite on the grain boundary in armcoiron. The austenite formed at the grain boundary of armcoiron showed hardening structure after annealing and quenching. The interpretation of the formation of austenite is possible by evaluation of the hardening structure. The areas of fracture resulting from the size and the distribution of the hardening structure is discussed. It is pointed out, that the area of fracture is a function of the size as well as of the distribution of the hardening structure.
    Notes: Der sich bei (Armco-)Eisen während der Glühung im α- + γ- Mischkristallgebiet an der Korngrenze gebildete Austenit zeigte nach dem Abschrecken Härtegefüge und entsprechende Härtewerte Ein Anlassen auf 500 °C führte zu einer Einformung des Zementits. Die Deutung der Austenitbildung ist nur indirekt über Rückschlüsse aus dem Härtegefüge, das bei Raumtemperatur untersucht werden kann, möglich. Die Wärmebehandlung beeinflußt auch Größe und Verteilung der Härtegebiete. Das Verformungsverhalten unterschiedlich wärmebehandelter Proben wird anhand von Aufnahmen, die mit einem Raster-Elektronenmikroskop gemacht wurden, besprochen.
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 225-232 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Development Trends in High Tensile Weldable Boiler and Pressure Vessel Steels. Increase of dimensions, pressure and temperature of boilers and pressure vessels necessitate the development of high tensile steels. To improve the tensile properties of steels water quenching and tempering (Q. T.) is applied more and more beside the addition of alloying elements.Results of tests on Q. T. micro- and low alloyed pressure vessel steels have been described. In addition to tensile and brittle fracture properties the behaviour of Q. T. Steels in creep tests, fatigue tests and intercrystalline corrosion tests has been reported on.Water quenching and tempering of boiler and pressure vessel steels offers technologically and economically favourable means of development.
    Notes: Die zunehmenden Abmessungen, Drücke und Temperaturen von Dampfkesseln und Druckgefäßen führen notwendigerweise zur Entwicklung höherfester Stähle. Zur Steigerung der Festigkeitseigenschaften wird immer mehr die Wasservergütung herangezogen. Es werden Ergebnisse von Untersuchungen an wasservergüteten mikrolegierten und niedriglegierten Druckbehälterstählen beschrieben. Außer den Festigkeitseigenschaften und der Sprödbruchsicherheit wird das Verhalten wasservergüteter Stähle bei Dauerstandsbeanspruchung, Dauerfestigkeitsbeanspruchung sowie hinsichtlich interkristalliner Spannungsrißkorrosion behandelt.Abschließend ist festgestellt worden, daß die Wasservergütung von Kessel- und Druckbehälterstählen eine technisch und wirtschaftlich günstige Entwicklungsmöglichkeit bietet.
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    Materialwissenschaft und Werkstofftechnik 2 (1971), S. 252-253 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Testing of soft-soldering properties of semi-manufactured metals. Suitable for carrying-out solderability tests of semimanufactured metals, especially of strips or sheets made of copper alloys, a simple apparatus has been developed, which permits the determination of the “critical immersion rate”, i.e. the immersion rate of a specimen with defined dimensions, at which a complete wetting with molten tin still occurs. The results obtained with this apparatus are reproducible and suitable for the assessment of the soft-soldering properties of materials to be soldered.
    Notes: Ein einfaches Gerät für die Prüfung der Lötbarkeit von Halbzeugen, insbesondere Bändern oder Blechen aus Kupferlegierungen, wird beschrieben, das die Bestimmung der “Grenztauchgeschwindigkeit”, d. h. der Tauchgeschwindigkeit einer Probe mit definierten Abmessungen, bei welcher noch eine vollständige Benetzung der metallischen Oberfläche mit Lötzinn erfolgt, ermöglicht. Die mit diesem Gerät erzielbaren Ergebnisse sind reproduzierbar und als Maß für die Verzinnbarkeit zu lötender Werkstoffe geeignet.
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