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  • 2015-2019
  • 1965-1969  (1.849)
  • Physics  (1.849)
  • 101
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1785-1809 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Infrared spectroscopic studies have been made of mixed crystals of linear polyethylene and perdeuteropolyethylene. On the basis of normal vibration analyses by Tasumi and Krimm it had been shown that the study of crystal splittings of internal chain modes in such mixed crystals could provide information on the geometry of chain folding. The present results, which include a study of n-paraffin (C36) mixed crystals, confirm these predictions. They show that (110) folding predominates in dilute solution grown crystals, and that this is transformed to (200) folding in melt-crystallized polymer. Folding with adjacent re-entry is favored, a random re-entry model being clearly eliminated.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 102
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A modus operandi is developed for determining the molecular structure of hydroxypropylcellulose (HPC), and characterizing, in quantitative terms, the morphological changes occurring when a water-cast film of the polymer is deformed. This involves the application of the following eleven different physical measurements: wide-angle x-ray diffraction, differential scanning calorimetry, density, melt rheometry, infrared spectroscopy, refractive index, birefringence, sonic modulus, small-angle light scattering, optical and electron microscopy. In addition, a computer was utilized as a mathematical diffractometer. Morphologically, water-cast HPC was observed to have structure at all levels, from the molecular to the supermolecular. The HPC molecule has a backbone of anhydroglucose units twisted into an irregular 31 helix. Intramolecular hydrogen bonding of the poly(propylene oxide) side chains leads to a stiff, rodlike molecule. The molecules are packed into microfibrillar crystallites 470 Å long and 34 Å in diameter. The microfibrils in turn, associate into supermolecular rodlike structures. The structural rearrangements that occur at each morphological level during deformation of HPC film are quantitatively examined and described.
    Zusätzliches Material: 36 Ill.
    Materialart: Digitale Medien
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  • 103
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1329-1355 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Mechanical relaxation has been studied at 0.67 cps in linear polyethylene (LPE) and polytetrafluoroethylene (PTFE) between -190 and -20°C. Specimens were prepared by use of various thermal treatments to produce in LPE a range of crystalline fractions from 0.690 to 0.825 and in PTFE from 0.615 to 0.870. An empirical theory is proposed relating the modulus of the crystalline-amorphous composite solid to the moduli and the volume fractions of the two phases. The empirical theory is shown to be in accord with the bounds of Hill and of Hashin and Shtrikman. The theory is used to determine the magnitudes of the crystalline and amorphous components of the low temperature relaxations in LPE and PTFE from measurements of logarithmic decrement and shear modulus. In PTFE the γ relaxation occurs in the amorphous fraction alone. In LPE the γ relaxation is a composite one, formed from the superposition of a small crystal relaxation and a large amorphous relaxation. For the crystal relaxation in LPE the ratio of relaxed to unrelaxed modulus equals 0.78; for the amorphous relaxation, the ratio equals 0.23. In a specimen of LPE with crystal fraction 0.69 the crystal contribution to the relaxation is 25% of the total. The magnitude of the unrelaxed modulus of the crystal fraction of LPE (modulus of polycrystalline LPE at -190°C) is in reasonable agreement with theoretical calculations of Odajima and Maeda.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 104
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2029-2041 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Drawing of single-crystal mats of linear polyethylene has been investigated. Drawing is possible at temperatures higher than about 90°C. The drawing is accompanied by distinct necking, with a large decrease in the thickness of the mat and a very high maximum draw ratio, sometimes over 30. The maximum draw ratio is approximately proportional to the thickness of the lamellae. This behavior strongly suggests the unfolding of chains during drawing. A change of orientation of crystal axes occurs before necking without change of lamellar orientation. The a axis orients in the drawing direction; the b axis orients perpendicular to the direction of drawing; and the chain axis tilts away from the thickness direction of the mat. The structure of films drawn from mats is characterized by a distinct double orientation of crystals. This biaxial orientation in the drawn films has a high degree of correlation with the orientation of crystal axes observed before necking, and suggests that necking takes place in such a way that the chain tilts gradually about the b axis and ultimately unfolds. The postulate of formation of transitory two-dimensional crystals in necking seems useful in explaining the double orientation in the drawn film. The orientation behavior of crystal axes observed before necking is not always similar to that observed in the deformation of a single crystal. The difference is thought to be due to the effect of forces induced by drawing that act in the direction normal to the lamellae within a mat.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 105
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1811-1818 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A “dual sorption” model has been proposed by Michaels, Vieth, et al. to explain extensive equilibrium sorption data for several gases in some glassy polymers. To explain data on sorption kinetics, it was further postulated that one of the sorption modes immobilizes the gas molecules. Stated mathematically, this model leads to a modified form of Fick's second law. Both normal and desorption time lags for diffusion have been computed here for this model of diffusion in glassy polymers. The computed time lags are shown to be dependent on the boundary concentrations used in permeation. Experimental measurement of these time lags would be a sensitive and critical test to ascertain the validity of this theory.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 106
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1863-1882 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly(methyl methacrylate) tensile bars were prepared containing nearly spherical polytetrafluoroethylene particles in concentrations from one to a thousand particles per gauge length of the bars. Particle diameters varied from 0.0035 to 0.018 in. Exhaustive tensile tests were performed at sufficiently high strain rate to assure brittle fracture and the results analyzed statistically by the theory of extreme values as proposed by Epstein. The results suggested that the polytetrafluoroethylene particles themselves did not act as flaws, but that they intensified the stress field on natural flaws which acted as the origin of fracture. Assuming a Laplace distribution as the underlying distribution of tensile strength (not to be confused with observed distribution of tensile strengths) gave predicted fracture statistics in good agreement with experiment.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 107
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2142-2143 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 108
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1895-1905 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A simple, practical calculation procedure has been developed for predicting the changes in molecular weight distribution of a polymer undergoing random crosslinking and/or degradation. Simulations of the random crosslinking and degradation of narrow and broad Poisson-type distributions have been made. The results agree with those calculated from Kimura's analytical solutions to Saito's general equations after a correction has been made for a mathematical error in Kimura's solution. This method can be applied to determining the probabilities of crosslinking and scission for any arbitrary molecular weight distribution expressed in tabular form. The importance of using narrow distribution samples to estimate crosslinking from changes in molecular weight distribution is graphically demonstrated.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 109
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 27-36 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Silica flocculated with a high molecular weight poly(DMVPMS) contains aggregates that are stable enough to permit size measurement with a Coulter counter. The average size of these aggregates increases up to a critical level of added polymer; the primary particles reappear at higher levels of added polymer. The aggregate size is reduced by continued mixing and the particle size distribution before flocculation is approached. Subsidence rates, equilibrium sediment volumes, and refiltration rates give somewhat different estimates of the degree of flocculation. Additional aggregation beyond that measured by the Coulter counter must be considered in the interpretation of these data. The decrease in floc strength during continued agitation is attributed to a disaggregation of the bridging polymer, to a decrease in the interparticle bonding of the bridging polymer, and to an increase in the surface coverage with polymer.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 110
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 357-375 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The assumed analogy between polymer solutions and polymer-network gels as regards the thermodynamics of swelling - a fundamental assumption implicit in all previous analyses of swelling measurements on gels, aimed at checking the statistical theories of rubber elasticity - is shown in fact to be rather limited. In particular, excluded volume effects, which play a dominant role in both solutions and gels, are quite different in the two types of systems. A new thermodynamic description of swelling equilibria, taking account of differences in excluded volume effects, is given, and analogies and differences between gels and solutions are pointed out.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 111
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 405-410 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Multiphonon contributions to the directional phonon frequency functions are calculated for crystalline polyethylene. These results are compared to previously calculated one-phonon frequency functions.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 112
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 743-745 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 113
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 749-749 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 114
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 763-773 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Triad tacticity data obtained by NMR analysis have previously been interpreted in terms of two basic statistical models in order to elucidate the stereospecific polymerization mechanism. In this paper the characteristics of these two basic models for stereospecific polymerization, the enantiomorphic-sites (EMS) model, and the polymer-end control (PEC) model, are examined and compared. The tacticity values accessible to the two-parameter EMS model, which includes the influence of the chain end unit, are shown to be highly restricted. Only about 20% of the isotacticity versus syndiotacticity plot is accessible to this model. To this extent the consistency of a set of triad tacticity data with the model can be tested. No such tacticity limits are exhibited by the two-parameter PEC model, which includes the influence of the penultimate unit. Any set of tacticity values which can be interpreted in terms of the two-parameter EMS model can also be interpreted in terms of the two-parameter PEC model.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 115
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 809-819 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A novel gas-flow method of measuring the diffusion, solubility, and permeability of gases and vapors in polymer films is described. The specific advantages of this system over the time-lag technique are discussed. Transport data, including activation energies and enthalpies of solutions, for hydrogen and deuterium in poly(vinyl fluoride) are presented, and the effects of the glass transition and of orientation on the observed transport rates are discussed.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 116
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 867-877 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: SynopsisThe diffusion of six solvents in three crosslinked, glassy epoxy polymers is studied. Case II swelling and Fickian sorption are observed as two simple limiting cases. The mechanism of diffusion changes from one limit to another as the nature of the solvent or the crosslink density of the polymer is altered. With mixed solvents, properly chosen, a superposition of Fickian diffusion and case II swelling is observed.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 117
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1005-1019 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements of T1ρ as a function of temperature have been made on three polyethylene oxides (PEO) with molecular weights of 550, 6000, and 2.8 × 106 in order to try to elucidate various problems arising in the interpretation of previous T1 measurements on PEO. In contrast to the T1 measurements, the T1ρ measurements show discontinuities at the melting or softening points of the respective polymers concerned, and also show nonexponential magnetization decay in the case of PEO 6000 and 2.8 × 106, which is presumbly due to the existence of “mobile” and “crystalline” regions, in qualitative agreement with NMR studies and x-ray measurements. Motional correlation frequencies and activation energies have been derived where possible by using the BPP theory adapted to the rotating frame and also the strong collision Slichter-Ailion theory. There is reasonable correlation with other data on motional frequencies where it is available, although the overall situation for the so-called α transition in PEO 6000 and 2.8 × 106 is still not clear. It is suggested that spin-diffusion is an important mechanism for all three polymers; for PEO 550 because it contains CH3 endgroups which act as sinks, and for the other two polymers where the mobile fraction performs the same function.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 118
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1405-1414 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Molecular motions in poly(vinylidene fluoride) were studied by the dielectric technique. Three distinct absorption peaks (αc, αa, and β) were observed in the frequency range from 0.1 cps to 300 kcps and in the temperature range from -66 to 100°C. The molecular mechanisms for these absorptions and their temperature dependence are discussed, and results are compared with x-ray diffraction and the NMR measurements. It is concluded that the αc absorption located at 97°C (1 kcps) is related to molecular motion in the crystalline region. The αa absorption located at -27°C (1 kcps) can be interpreted as due to the micro-Brownian motion of the amorphous main chains. The β absorption located at -47°C (1 kcps) is attributed to local oscillation of the frozen main chains.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 119
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1444-1449 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 120
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1451-1459 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The adiabatic compressibility for two samples (F-1 with DP-3748 and F-2 with DP-2114) of poly(4-vinyl-N-n-butylpyridinium bromide) in aqueous solution has been determined from ultrasonic velocity and density data. The sample (F-1) with the higher degree of polymerization shows comparatively higher velocity and density in solution. However, the evidence for the difference in compressibility is not very decisive. The apparent molal volume ΦV2 and apparent molal compressibility ΦK2 for F-1 are found to be slightly higher than for F-2. In aqueous solution, the decrement of adiabatic compressibility per unit concentration, (β1 - β)/c, is found to be almost constant throughout the entire concentration range, whereas in the presence of excess added electrolyte (1.0M KBr solution), the compressibility decrement shows a decrease with dilution. The latter values are lower than those found in water, since the molecules, in the presence of excess electrolyte, are coiled up more and are less compressible. The ΦV2 and ΦK2 values in water are constant throughout the entire concentration range, as the free counterions formed on dissociation in the dilute region are not solvated and hence contribute little to the compressibility. On the other hand, in the presence of excess KBr (1.0M), the ΦV2 and ΦK2 values show a sharp decrease with increase of polyelectrolyte concentration and finally attain a constant value. This is explained by the fact that because of the formation of a charge-transfer complex between the bromide ion and the polycation, more than the equivalent number of bromide ions is bound, leaving free an equal amount of K+ ions which are solvated and cause the lowering of apparent volumes and compressibilities. Condensation of charges begins at a certain polyelectrolyte concentration, and no further increase of K+ ions is observed. A special situation arises in 0.1M KBr solution. The ΦV2 and ΦK2 values at first increase sharply with increase of polyelectrolyte concentration, but then level off to attain a constant value, at comparatively high concentration. In 2.0% poly(4-vinyl-N-n-butylpyridinium bromide) solution, the concentration of polymer repeat unit (0.08M) is almost equal to the concentration of the added electrolyte (0.1M KBr) used to suppress dissociation. As the polyelectrolyte concentration in 0.1M KBr solution is progressively decreased, more bromide ions are made available for forming the charge-transfer complex with the polycation, leaving the K+ ions free to contribute to the compressibility.
    Zusätzliches Material: 4 Ill.
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  • 121
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1495-1511 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements are reported of the vapor pressures and the heats and volumes of mixing of solutions of poly(ethylene glycol dimethyl ether) in chloroform and in carbon tetrachloride. The measurements have been used to calculate the thermodynamic mixing functions for mixing with zero volume change. These values have been compared with the predictions of the lattice theory of mixtures at three different levels of approximation, viz., the generalized “first approximation” theory of Barker, the “zeroth approximation” theory, and the Flory theory. In the hydrogen-bonding chloroform solutions the Barker theory is more successful than the other forms of the lattice theory. The results have also been used, in conjunction with those for solutions of poly(propylene glycol dimethyl ether) in the same two solvents, to test the ability of the Barker theory to correlate the properties of related systems. Good correlation is found between the two carbon tetrachloride solutions but not between the chloroform solutions. It is probable that the side-chain methyl groups in the propylene oxide repeating unit cause the hydrogen-bonding interaction to be weaker in this polymer than it is in the polymer with the ethylene oxide repeating unit.
    Zusätzliches Material: 5 Ill.
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  • 122
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1559-1575 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Dielectric constant and dielectric loss of copolymers of methyl methacrylate (MMA) with n-butyl methacrylate (nBMA) and isobutyl methacrylate (iBMA) have been measured in the frequency range 30 cps to 1 Mcps at temperatures from 70°K to 370°K. Results lead, together with those of previously published investigations on copolymers of MMA, to the following conclusions. (1) The loss-peak temperature attributed to side-chain relaxation (β peak) of PMMA varies with the comonomer ratio when the comonomer does not have an α-methyl group, but remains almost unchanged for comonomers having an α-methyl group. (2) In both cases, the β peak height of PMMA decreases with increasing ratio of comonomer B and completely vanishes for poly-B, and the loss peak temperature plotted against the fraction of B does not extrapolate to the β peak of poly-B. It is suggested on the basis of the above facts that the moving unit in the side-chain relaxation consists of a single side chain with a segment of the backbone chain and that the change in mobility of the side chain upon copolymerization results from the distortion of the helical structure of the backbone chain due to random distribution of α-methyl groups. Dielectric studies of the low-temperature side-chain relaxation (β2 peak) in PnBMA, poly(n-octyl methacrylate), and poly(n-dodecyl methacrylate) (130°K at 1 kcps) have been made and an interpretation is offered for the molecular nature of this relaxation.
    Zusätzliches Material: 21 Ill.
    Materialart: Digitale Medien
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  • 123
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1627-1638 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new type of long-range interaction between chain segments and solvent molecules in a polymer molecule is introduced. It can be depicted as an “interfacial” free energy, due to the more or less diffuse interface between the interior of a polymer coil and the surrounding solvent. Flory's calculation of the coil expansion α is extended for this effect, by using theoretical approaches developed by van der Waals, Cahn and Hilliard, and Debye for inhomogeneous systems (interfaces). It is found that Flory's equation for α is replaced by: \documentclass{article}\pagestyle{empty}\begin{document}$ \alpha ^5 - \alpha ^3 = 2C_M \psi _1 M^{1/2} \left[ {1 - \left( {\theta /T} \right) + \left( {15/2\alpha ^2 } \right)\left( {\theta /T} \right)\left( {l^2 /\overline {r_0^2 } } \right)} \right] $\end{document} where the last term is due to the “interfacial” free-energy correction. The Debye molecular interaction length l is also found in theories on light scattering of binary mixtures near the critical solution temperature. An important result of this equation is that at T = θ, α is not equal to unity, as before, but somewhat larger, depending on the molar mass of the polymer and the solvent type. A calculation shows that the “interfacial” free energy correction may contribute substantially to the “solvent” effects on the expansion of a polymer molecule at the θ temperature, as has recently been reported in the literature.
    Materialart: Digitale Medien
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  • 124
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1695-1704 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The Hv cloverleaf scattering pattern sometimes found for amorphous polymers can arise from the birefringent region caused by the strain surrounding a void or an inclusion in a polymer. The form of such a pattern may be theoretically explained by extension of a theory due to Goldstein.
    Zusätzliches Material: 6 Ill.
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  • 125
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1735-1744 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The infrared absorption of poly(ethylene glycol) was measured in the molten state. Characteristic bands of the molten state were identified. Normal vibrations and frequency distributions were treated for various conformation models with CH2CH2O repeat units. The infrared absorption peaks of the molten state closely correspond to the frequency distribution peaks of the TGT conformation with gauche O—CH2—CH2—O groups, although infrared bands due to trans O—CH2—CH2—O groups are also observed. Vibrational assignments of the infrared bands and Raman lines were made on the basis of potential energy distributions.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 126
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1761-1773 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Thermogravimetric Analysis (TGA) is finding increasing utility in investigations of the pyrolysis and combustion behavior of materials. Although a theoretical treatment of the TGA behavior of an idealized reaction is relatively straight-forward, major complications can be introduced when the reactions are complex, e.g., in the pyrolysis of cellulose, and when experimental imperfections arise. Consequently, a fairly large number of analytical methods have been proposed for obtaining kinetic parameters from TGA curves. Among the proposed methods are several graphical procedures, mostly involving relatively inaccurate tehniques, such as obtaining slopes on a rapidly changing curve. Included among the proposed procedures is one which permits a linear plot of TGA data. The sensitivity with which such a plot can be used to identify and correct for a variety of experimental complications seems to have escaped even the proponents of the techniques. This paper provides an illustration of the use of this graphical procedure in a hypothetical first-order pyrolysis typical of those occurring in the TGA behavior of cellulose.
    Zusätzliches Material: 10 Ill.
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  • 127
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1819-1833 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Annealed polyethylene single crystals have been degraded with fuming nitric acid, and the molecular weight distribution of the fragments determined by using a gel-permeation chromatograph. Peaks due to chain folding were observed in these distributions as for unannealed single crystals. The peaks moved to lower molecular weight with increasing degradation time. Comparison of the lowest molecular weight peak length after a given degradation time with the low-angle x-ray periodicity before degradation gave information about a disordered surface layer. The thickness of this layer at early states of degradation was dependent solely on annealing temperature, though changes in the layer must have occurred with annealing time, since there was an increase in reaction rate with annealing time. At higher degradation states, the thickness of the layer was dependent solely on the original low-angle periodicity. This has been related to the depth at which some folds are buried beneath the lamellar surfaces. The relevance of these observations to the structure of annealed single crystals is discussed.
    Zusätzliches Material: 8 Ill.
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  • 128
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1955-1964 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The intrinsic viscosity ratio [η]B/[η]L was calculated as a function of average branching density for trifunctionally branched, free-radical polymers. Calculations were made for the g1/2, g3/2, and h3 rules, using realistic distributions of molecular weights and branches. Experimental data on branched poly(vinyl acetate) lay between the curves obtained from the g1/2 and h3 relations.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 129
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2019-2028 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The diffusion studies of several solvents in epoxy polymer reported by Kewi and Zupko in Part I of this series are explained with the solution obtained from the generalized diffusion equation which includes the internal stress contribution. The rate of permeation of a penetrant through a polymer film and the time lag needed to reach steady state are also given for the generalized diffusion equation.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 130
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2043-2050 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: This is the first paper of a series of reports concerning extended-chain crystals of flexible, linear high polymers. The general conditions for crystal growth are discussed. Polymer crystallization is described as a two-step process: nucleation of each crystallizing molecule to a folded-chain conformation, followed by an increase in fold length in a solid-state reorganization step. This reorganization step is enhanced in the case of polyethylene by crystallization at high temperature under elevated pressure. Mechanical deformation during crystallization is also able to produce extended-chain crystals. The most promising method, however, is crystallization during polymerization. Previous work on crystallization of polyethylene under elevated pressure is critically reviewed.
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  • 131
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2091-2097 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Differential thermal analysis and electron microscopy of partially molten, extended-chain polyethylene crystals, grown under elevated pressure, was performed. It could be shown that melting peaks on the low temperature side of the main melting peak are due to narrowly distributed, low molecular weight polymer segregated in extended-chain crystals. Superheating of crystals before melting increased with molecular weight and chain extension. The melting mechanism of extended chain crystals was shown to be a successive peeling off of chains which leaves the chain extension constant up to melting of the last crystal trace.
    Zusätzliches Material: 6 Ill.
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  • 132
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2140-2141 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 133
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 37-45 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The well known procedure of determining the degree of crystallinity by means of measuring the density presupposes the knowledge of both the densities ρc and ρa of the crystalline and of the noncrystalline regions. By combination of small-angle and wide-angle x-ray scattering and of density measurements it can be shown that this method is not justified in the case of drawn polyethylene if the values of ρc and ρa known from isotropic material are used. Both ρc and ρa depend considerably on annealing and drawing conditions. In addition the effective density ρc* of the more densely packed phase in a two-phase structure is much lower than the value ρc calculated from the positions of the x-ray reflections due to a large number of lattice defects. This conclusion is based on the results of three independent sets of experiments: determination of the mean-square fluctuation of density 〈η2〉 by means of x-ray small-angle scattering; x-ray wide-angle measurements of the positions of the crystal reflections and of the halo arising from the noncrystalline regions; and comparison of densities and long periods of samples treated at various annealing temperatures.
    Zusätzliches Material: 4 Ill.
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  • 134
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 123-142 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Isothermal and nonisothermal spherulitic crystallization in even-odd and poly(ω-aminocarboxylic acids) has been studied for a range of fusion conditions and solidification temperatures. The variety of spherulites so formed are classified mainly by optical microscopy. It is found that polyamides with similar types of repeat units generally exhibit similar morphological features under corresponding crystallization conditions. The basic patterns are illustrated in the text. Changes in spherulitic birefringence with temperature are also discussed. In some cases, at temperatures not far below the polymer melting point, platelet-like crystalline aggregates are formed in thin film preparations. These platelets exhibit properties characteristic of single crystals.
    Zusätzliches Material: 19 Ill.
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  • 135
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A general description is given for relations among the optical quantities obtained from fluorescence polarization measurements on bulk polymer stained by fluorescent groups: the moments of distribution of orientations of the fluorescent groups, and those of the structural units of the polymer (chain segments) on which the groups are adsorbed. Two assumptions as to the biaxial symmetry of the bulk polymer and the cylindrical symmetry of the optical anisotropy of the fluorescent element, both for the absorption and emission processes, reduce the intensities of the polarized fluorescence to a 3 × 3 matrix L which is asymmetric (Lij ≠ Lji), as has frequently been observed in experiments. The components of the L matrix are related to those of the J matrix which is so defined as to describe the fourth moments of the distribution of orientations of the structural units on the basis of a random distribution of the rotational angle of the unit about the segment axis. It is found that the use of the method of fluorescence polarization combined with absorption dichroism and/or emission gives the values of the optical anisotropy ratios of the fluorescent unit, and that the effects of the thermal agitation of the structural unit can be separated from the moments of the orientation distribution for the simplest case.
    Zusätzliches Material: 2 Ill.
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  • 136
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 747-748 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 137
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 753-762 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Eight epoxy-diamine networks have been formed, diamines with 2 to 12 methylene groups being used as curing agents. Dynamic mechanical tests revealed four transition regions in the dynamic loss modulus/temperature relationship. Two possible explanations for the relaxation of the glycidyl portion of the structure are proposed. One of the relaxations could be due to the breakdown of hydrogen bonds through the hydroxyl and ether groups. The second could be ascribed to the relaxation of the unbonded glycidyl groups or a second relaxation of the glycidyl groups after the breakdown of the hydrogen bonds.
    Zusätzliches Material: 2 Ill.
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  • 138
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 783-794 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Previous theoretical calculations of elastic constants for cellulose based on force constants for bond stretching and bending of valence angles have yielded axial stiffness values admittedly too low. The present analysis accounts for a hitherto unexamined geometrical effect associated with deformation of interchain hydrogen bonds. To do this, most primary bond deformations are neglected so the resulting calculation gives an upper bound for the axial stiffness. By using two different sets of hydrogen bond force constants, values of 24.6 and 31.9 × 1011 dyne/cm2 were obtained for Young's modulus in the chain direction. These values are very much larger than earlier calculations and experimental determinations from cellulosic fibers, indicating both the importance of the effect considered here and the likelihood of an exact analysis yielding an acceptable result.
    Zusätzliches Material: 6 Ill.
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  • 139
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 423-424 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 140
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The mechanical anisotropy of regenerated cellulose films is investigated, first, on the basis of the theory of infinitesimal elasticity. Fairly good agreement of calculated with observed results is obtained on the basis of orthogonal anisotropy with respect to the machine direction and the transverse and thickness directions of the films. The shear modulus G23 along the film plane and the Poisson ratio v32 are 1.5 times; 102 kg/mm2 and about 0.4, respectively, in the standard dry state. Second, the mechanical anisotropy in three different dry states is analyzed in terms of the degree of biaxial orientation of two kinds of structural units, cellulose II crystallites and noncrystalline chain segments, and their mechanical anisotropy. The calculation for averaging the mechanical anisotropies of these structural units on the basis of the homogeneous strain hypothesis gives results much higher than the experimental data, whereas the calculation on the basis on the homogeneous stress hypothesis gives results rather lower than experiment. As a modification of the two extreme calculations, a different averaging gives considerably better agreement between the calculated and observed results. The mechanical anisotropy in the wet state is further analyzed primarily in terms of the degree of biaxial orientation of noncrystalline chains by a modification of Krigbaum treatment, based on application of the kinetic theory of entropy elasticity for semicrystalline polymers, to anisotropic systems. The calculation gives results, however, much lower than those obtained experimentally, unless the ratio of the end-to-end distance of the noncrystalline chain to its fully stretched length is taken as unusually large. This may be due to underestimation of the contribution of the crystalline phase to terms of the same type as appear in the Krigbaum treatment.
    Zusätzliches Material: 12 Ill.
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  • 141
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 425-427 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 142
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 525-536 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The dynamic shear behavior of four highly amorphous polymers in the unstretched and stretched states (draw ratios 3:1 to 6:1) was investigated with a torsion pendulum at temperatures from 4.2°K to 180-300°K and frequencies from 0.4 to 3.2 cps. The polymers studied were polystyrene, poly(vinyl acetate), poly(vinyl propionate), and poly(isobutyl vinyl ether). Previously unreported loss maxima were found at 48°K (1.5 cps) and 149°K (1.3 cps) for poly(vinyl proplonate), at 10°K (1.0 cps) for poly(vinyl acetate) and at 9°K (1.6 cps) for poly(isobutyl vinyl ether). Uniaxial orientation increased the shear storage modulus G, measured with the torsion axis parallel to the stretch direction and caused changes in the loss peaks which depended on the polymer material studied.
    Zusätzliches Material: 10 Ill.
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  • 143
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 551-561 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Small-angle x-ray scattering studies were made on bulk-crystallized samples and annealed oriented films of TMPS. The temperature dependence of the small-angle scattering was determined over a range of annealing conditions. The effect of sample molecular weight on the small-angle peaks was also studied. The peak intensity, measured at room temperature after annealing, was strongly dependent on the annealing conditions. The position of the peak gradually moved to smaller angles (larger d spacings) as the annealing temperature was raised. Surface free energies were deduced from the melting point dependence of the crystallite size. This surface energy was found to increase with molecular weight in accord with values deduced for spherulite growth rate-temperature dependence.
    Zusätzliches Material: 6 Ill.
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  • 144
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 593-600 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A model is proposed to account for the regular twisting of radial ribbons in certain polymer spherulites. The model assumes that the ribbons have crystallographically regular fold surfaces and that growth of the ribbons is nucleation-controlled. The model leads directly to a possible mechanism of spherulitic growth in some polymers.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 145
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 659-666 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A specimen of linear polyethylene was subjected to isothermal secondary crystallization at a series of temperatures below the primary isothermal crystallization temperature, the melting and primary crystallization stages being held constant throughout the investigation. Dilatometric measurements exhibit an S-character at low values of undercooling Tp - Ts, where Tp and Ts are, respectively, the primary and secondary crystallization temperatures; at larger undercoolings, however, an initial very rapid crystallization is followed by a very slow stage. When corrected for thermal contraction of the polymer, the net degree of secondary transformation is seen to peak at a temperature in the range 109-113°C. The S-character of the isotherms and the peaked temperature variation of degree of transformation lead to the conclusion that a large portion of the secondary crystallization consists of the nucleation and growth of the new crystallites. Johnson-Mehl-Avrami analysis leads to a model of heterogeneous nucleation within the remaining amorphous zones, followed by one-dimensional, diffusion-controlled growth.
    Zusätzliches Material: 4 Ill.
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  • 146
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 675-685 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The strength and extensibility of an unfilled styrene-butadiene rubber vulcanizate were determined in constrained biaxial tension (essentially pure shear) by stretching thinwalled cylindrical specimens in the axial direction with an Instron tester while gas pressure was admitted to maintain constant the outside diameter of a specimen. The rupture stress, λ1b, and the extension ratio, λ1b, in the axial direction and the rupture stress, σ2b, in the circumferential direction were determined at extension rates from 0.0031 to 3.1 min-1 and temperatures from 25 to 90°C. Rupture data in simple tension were also obtained by testing ring specimens under similar test conditions. The time-temperature shift factor, aT, obtained by superposing rupture data at different temperatures, gives a constant activation energy of 35 kcal. Doubly logarithmic plots were prepared showing the dependence of σ1b/λ1b, σ2b, and λ1b from the biaxial tensile tests and of σb/λb and λb from the simple tensile tests on the temperature-reduced extension rate, \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \lambda a_T $\end{document}. (The quantities σ1b/λ1b, σ2b, and σb/λb are rupture stresses based on the dimensions of undeformed specimens.) At equal values of \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \lambda a_T $\end{document}, the extension ratios λ1b and λb are sensibly identical. The ratios σ1b/σb and σ2b/σb, as well as λbσ2b/σb, were obtained from rupture data read from the composite curves at selected values of \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \lambda a_T $\end{document}. Also, similar ratios were derived from stress data at equal extensions in biaxial and simple tension for 1.25 ≤ λ ≤ 3.0, the range comparable to that in which rupture data were obtained. A consideration of the ratios given by both the rupture and the stress data shows that the von Mises failure criterion is not applicable, although the departure is small except at the larger values of λb.
    Zusätzliches Material: 7 Ill.
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  • 147
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1651-1667 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The plastic deformation of poly-4-methylpentene-1 (P4MP1) crystals on a unidirectionally drawn substrate has been investigated by electron microscopy. In addition to cracks spanned by fibrils and buckling perpendicular to the stretch direction, both features found in deformation studies of other polymers, a unique slip mechanism leading to sectorization of P4MP1 crystals is observed; deformation was also found to occur by means of localized lamellar thinning. The exact type of plastic deformation occurring in P4MP1 crystals is found to depend on the orientation of the lamellae with respect to the tensile axis. Some evidence for a periodicity on the fibrils studied is given.
    Zusätzliches Material: 15 Ill.
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  • 148
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1033-1057 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The phenomenon of double melting, as manifested by two characteristic endotherms in the melting region on a differential thermal analysis (DTA) scan, has been studied in nylon 66 and polystyrene as a function of sample treatment by annealing or drawing. A variety of techniques were used in these studies including DTA, x-ray diffraction, electron microscopy, and mechanical testing. It is shown that the two endotherms are not caused by a bimodal crystal size distribution, by recrystallization, by orientation changes, or by phase changes. It is proposed that one endotherm is caused by the melting of foldedchain crystals, while the other is due to the melting of less perfect bundle crystals. This view is well supported by the results, especially by the DTA measurements made at different heating rates. Published data on the thermal behavior of annealed and drawn poly(ethylene terephthalate) and on polyethylene crystallized at various pressures may also be explained on this basis if it is allowed that in polyethylene the chains may be more extended.
    Zusätzliches Material: 15 Ill.
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  • 149
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1165-1186 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The proton spin-lattice relaxation times (T1) of linear polyethylenes (PE) of varying morphology were measured as a function of temperature. The T1 of oriented bulkcrystallized and solution-crystallized material was isotropic, in disagreement with calculations based on a sample dipole pair model. Motion in the non-crystalline regions of the samples is shown to be responsible for the T1 minimum occurring around -20°C. The dependence of T1 at the minimum on the long period reinforces the model of an amorphous fraction composed of disordered lamellar surface layers. The temperature of the T1 minimum and the dependence of T1 on the long period imply that the mobility of these amorphous regions is reduced in cold-drawn and solution-crystallized samples. This mobility irreversibly increases with annealing. In highly relaxed samples the motion of a small portion of the disordered regions is almost liquidlike, as indicated by the presence of a second shorter T1.
    Zusätzliches Material: 12 Ill.
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  • 150
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1987-1994 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The thickness of the interphase layer as a function of time at 160°C has been determined directly in a microheterogeneous polymer mixture, and the layer thickness between two bonded sheets has also been measured by phase-contrast microscopy. Two mixtures of polymers, isotatic polypropylene with polyethylene and poly(vinyl chloride) with polyethylene, were prepared by mixing size-sorted powders in suspension, followed by evaporating the suspension medium and compacting the powdered mixtures. The mutual penetration initially obeyed Fick's second law; then diffusion was retarded and stopped after 15-20 min. An equilibrium state was reached which did not correspond to the classical thermodynamic equilibrium, at which the so-called equilibrium thickness of the interphase layer for the pair isotactic polypropylene-polyethylene was about 28,000 Å and for the pair poly(vinyl chloride)-polyethylene was about 89,600 Å. The equilibrium values can be used as a quantitative criterion for the compatibility of the polymer pairs.
    Zusätzliches Material: 3 Ill.
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  • 151
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1385-1392 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Shear viscosity and dielectric dispersion measurements have been made on a series of concentrated solutions of poly-p-chlorostyrene in toluene, chlorobenzene, and diethylbenzene, as well as on the pure polymer. It is found that the product ηνm/T is nearly temperature-independent in the present range of measurement (30 ≤ νm ≤ 30 ≤ 104 Hz), where νm is the frequency at which the dielectric loss maximum occurs. For the pure polymer, ηνm (200/T) is 1011.5 poise/sec. This leads to a segmental jump distance of 5 Å. Although the results in this range correspond quite well to the concept of a segmental friction constant determined by the matrix viscosity, deviations appear as the apparent energy of activation for viscous flow decreases below 13 kcal/mole. There is reason to believe that these deviations reflect the increasing importance of bond rotation barriers at low matrix viscosity. It is speculated that the damped torsional oscillator interpretation of f0 proposed by Tobolsky will become valid in systems still more fluid.
    Zusätzliches Material: 5 Ill.
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  • 152
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new light-scattering experiment which allows a direct determination of the conformation of macromolecules deformed in flow is described. Light-scattering relationships based on the interference function are developed, and results of an experimental study are detailed. The deformed conformation of high molecular weight polyisobutylene was determined in a Couette-type shear field. Decalin was the solvent. Variables investigated were the shear rate (0 to 600 sec-1), the polymer molecular weight (1.0 × 107 to 1.6 × 107), and the polymer concentration (2.0 × 10-4 to 8.0 × 10-4 g/cc). Conformation variables determined were the orientation of the molecule in the shear field and its maximum and minimum extension ratios in the plane defined by the direction of flow and the direction of the shear rate. The deformation of the macromolecule was found to be markedly discrepant when compared to the dynamic macromolecular models which assume complete coil flexibility, and more closely in agreement with the recent theories of Cerf, developed for nonfree-draining coils which exhibit a finite internal viscosity.
    Zusätzliches Material: 10 Ill.
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  • 153
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1439-1443 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 154
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1473-1481 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The mechanical and dielectric low temperature absorptions of poly(vinyl chloride) (PVC) and several modified PVC's have been studied over the temperature range from -60 to +60°C. with some tests extending to -150°C. and others to +170°C. The results indicate that the low-temperature absorption near -50°C (β2 absorption) decreases in intensity with chlorination, while the absorption at a higher temperature near 0°C (β1 absorption) decreases in intensity with hydrogenation. The apparent activation energies of the β1 and β2 absorptions were calculated to be 16 kcal/mole and 10.7 kcal/mole, respectively. Besides, the β2 absorption markedly decreases in intensity with addition of plasticizer, while the intensity of β1 absorption is not much affected by increasing plasticizer content. From these results, the β1 and β2 processes are concluded to be the results of molecular motion in crystalline and amorphous region in PVC, respectively. For samples of reduced Cl content, another low-temperature absorption was located near -120°C (γ absorption) and attributed to the presence of short sequences of ethylene units. It has also been observed that the temperature location of the high temperature absorption near 100°C (α absorption) shifts linearly to higher temperature with increasing chlorine content and to lower temperature with increasing hydrogen content.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 155
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1513-1523 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Six homologs of the cellulose triester series were found to exhibit, in general, three second-order transitions as determined dilatometrically. A parallel study of torsional modulus versus temperature revealed one glass-rubber transition, which allowed molecular assignment of one of the above. The dependence of the remaining two transition temperatures on length of the ester group permits some speculation with regard to their origin. The glass-rubber and secondary transitions exhibit an inversion for cellulose trivalerate and higher homologs, the two secondary transitions occurring at temperatures higher than the glass-rubber transition. A possible explanation for this anomaly in terms of side-chain crystallization is discussed.
    Zusätzliches Material: 5 Ill.
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  • 156
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1577-1583 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Melting temperatures were observed visually for poly-(2,6-dimethyl-1,4-phenylene oxide) in methylene chloride at nine concentrations (polymer weight fractions ranging from 0.0042 to 0.2362). The data were analyzed upon the assumptions that ΔHu and ΔSu, the molar heat and entropy of fusion per polymer unit, are constant over the temperature range studied, and that a Flory-Huggins chemical potential expression with a concentration-independent pair interaction parameter, χ1 = (0.5 + ψ1) + ψ1Φ/T, satisfactorily describes the polymer unit activity in the binary solutions. Computation gave ΔHu = 1404 cal/mole of units (therefore Δh = 11.7 cal/g), ψ1 = -0.5691, and Φ = 342.4°K. The effect of using various combinations of data points upon the values of these three parameters, as determined by least-squares linear regression treatment of the melting temperature expression, is indicated.
    Zusätzliches Material: 1 Ill.
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  • 157
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1595-1618 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A combination of electron-microscopy, light-scattering, and stress-birefringence studies on chemically crosslinked polyurethanes point toward the existence of rodlike regions (“bundles”), approximately 3000-8000 Å in length and involving about 5% of the volume, in which molecular orientations are correlated. The elastic behavior of these networks - as indeed that of most rubberlike networks - deviates substantially from the Gaussian behavior. The empirical representation of the data in Mooney-Rivlin plots yields C1 and C2 constants which depend on the type of imposed strain. It is thus impossible to identify C1 with the Gaussian behavior and C2 with the deviation there-from. Instead, it is found that the elastic behavior can be adequately described if it is assumed that, as a result of the bundle structure, about 5% of the segments of each chain are not free to assume the normal random-walk configurations. The determination of the number of chains in the network from the elastic behavior remains ambiguous, however, and the behavior upon swelling is not (yet) adequately reproduced by the theory. It is conceivable that in many cases deviations from Gaussian elasticity behavior may be caused by an intermolecular structuring effect, rather than by various minor deficiencies in the Gaussian model for the single chain statistics or by anisotropic excluded volume effects, as has been proposed in the past. In the present case, the amount of bundle structure, as well as the C2/C1 values, increase with the number of urethane couplings per chain, and this suggests that the interaction of the highly polar urethane couplings is responsible for the structuring. In other networks one often finds a dependence of C2/C1 on the previous history of the sample, which suggests that an accidentally trapped order may be responsible for the elastic behavior.
    Zusätzliches Material: 8 Ill.
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  • 158
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1639-1649 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The melting transitions of both crystalline forms of trans-1,4-polyisoprene, as detected by differential thermal analysis, have been identified by attendant studies with optical microscopy and x-ray diffraction. The lower-melting (LM) form melts initially at a temperature which depends upon the crystallization temperature but which, under our experimental conditions, is between 45 and 53°C. If recrystallization is allowed to occur, the apparent final melting point, which depends upon the recrystallization temperature, is about 58°C. The initial melting point of the higher-melting (HM) form, also crystallization temperature-dependent, is upwards of 57°C. Under the most easily accessible experimental conditions, it may be obscured by the final melting of the LM-form. The apparent final melting point of the HM form is approximately 66°C. Conversion of the LM form into the HM form occurs only by fusion and crystallization. No evidence of a solid-solid transition was found. The rate of conversion is governed principally by the rate of nucleation at the conversion temperature. If fusion of the LM form is incomplete, recrystallization of the LM form takes place instead of conversion to the HM form.
    Zusätzliches Material: 9 Ill.
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  • 159
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1995-2004 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Solution characterization measurements indicate that cylization of the polyamic acid from 2,4-diaminoisopropylbenzene and pyromellitic dianhydride (PMDA) to the polyimide can be effected with small change in number-average degree of polymerization. An increase in weight-average molecular weight on conversion to polyimide is attributed to branching side reactions. Inherent viscosities of polyimides from 4,4′-diaminodiphenyl ether and PMDA decreased slowly with time in concentrated (97%) sulfuric acid, probably as a result of hydrolytic cleavage. The zero-time viscosity intercepts were related to both the precursor and the estimated polyimide molecular weight. The latter gave ηinh (c = 0.5% solids) = 2.76 × 10-3M̄0.53w for 60,000 〈 Mw 〈 300,000. The exponent is near the lower limit of 0.5 found in theta solvents. The characteristic ratio of the root-mean-square end-to-end distance of a chain to the square root of its molecular weight is 1.1 Å and the steric factor is 1.1; these results suggest that the unperturbed polyimide chain is almost as extended as an equivalent freely rotating chain, a general feature of long-bonded polymers with p-phenylene rings in the chain backbone.
    Zusätzliches Material: 5 Ill.
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  • 160
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2051-2059 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A report on crystallization of polyethylene at elevated pressures to an extended-chain morphology is presented. The crystals have been characterized by electron microscopy and density determination. Pressure, supercooling (temperature), and crystallization time have been varied to find the best conditions for production of perfect crystals. At 10-30°C supercooling completely crystallized polyethylene was obtained between 4.5 and 7 kb crystallization pressure in 1-8 hr. Analysis of fracture surfaces of samples crystallized for different lengths of time shows an increase in size and number of crystal lamellae and an improvement of extended chain crystals in the early stages of crystallization. A further improvement of the less well crystallized material between the lamellae occurs after 15 min of crystallization time.
    Zusätzliches Material: 5 Ill.
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  • 161
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2099-2113 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Polyethylene crystals of different degrees of perfection were annealed at 5.1 kb pressure for 20 hr at various temperatures and analyzed by electron microscopy, thermal analysis, and density determination. No annealing took place until the temperature was close to the melting point of the starting material. Up to 235°C increasing solidstate annealing was observed. Mixed crystals of up to 0.989 g/cm3 density and 1500 Å thickness in the chain direction could be produced. At slightly higher temperature recrystallization to extended-chain crystals rather than annealing occurred. The annealing process at atmospheric pressure seems to be similar in nature, but takes much longer for comparable perfection. From a comparison of annealing and crystallization it is concluded that polymer crystallization goes through a stage of internally imperfect order during which most of the observed chain extension occurs. Estimates of this outer imperfect layer of a growing crystal place its depth at 30,000 Å.
    Zusätzliches Material: 9 Ill.
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  • 162
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 2141-2142 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 163
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 77-86 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The random depolymerization model of Montroll and Simha for originally homogeneous polymers is derived analytically by utilizing a weight distribution function approach not requiring the use of any approximations. The model is then extended to consider heterogeneous initial chains having an arbitrary chain length distribution. The probabilities for breakage are assumed to be identical for all bonds joining monomeric elements in the system and to be independent of chain length and position in the chain, assumptions also used in the model of Montroll and Simha. An expression is found for estimating the probability of bond breakage.
    Materialart: Digitale Medien
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  • 164
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 113-122 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Differences in structural parameters, shrinkage, and retractive forces have been compared for nylon 66 tire yarns annealed at several temperatures in silicone oil and in air. It is found that significantly different structural changes occur for oil-annealing and air-annealing. Retractive forces measured in hot oil are characterized by a high initial force, followed by a rapid decay and a second, more gradual, increase which is also followed by a decay at sufficiently high temperatures. In heated air, the first, short-term, retractive force is absent. It is postulated that these differences are due to the different rates of heat transfer at gas-solid and at liquid-solid interfaces, and that rapid heat transfer (as in the case of oil-annealing) promotes two mechanisms of molecular change which are characterized by different degrees of structural parameter change, and by different amounts of shrinkage.
    Zusätzliches Material: 5 Ill.
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  • 165
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 163-170 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A resolution index for gel-permeation chromatograph (GPC) columns is defined by the relation log (RI) = αW, where RI is the resolution index, α is the slope of the calibration curve of logarithm of molecular weight against peak position for narrow polymer fractions, and W is the width of the GPC curves for narrow fractions. This resolution index is calculated approximately for several GPC columns individually and in series combinations by using data obtained on narrow fractions of polystyrene. The index increases with number of columns and with flow rate over a limited range of flow rate, does not vary much with solvent, and does not correlate well with plate count obtained with low molecular weight molecules. It is believed that the resolution index provides an improved indication of the performance of GPC columns.
    Zusätzliches Material: 2 Tab.
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  • 166
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 219-229 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The compressibility of polyisobutylene and polystyrene above their glass transition temperature is treated as the sum of two parts; a free-volume compressibility and, as originally suggested by Bridgman, a compressibility of the molecules themselves. Two different models are used to treat the free-volume compressibility, and as a result values for the molecular compressibility are estimated. These are in reasonable agreement with other values in the literature. The magnitude of this “molecular compressibility” is then considered in relation to some existing treatments of intermolecular forces. These suggest that intermolecular contacts are more compressible than covalent bonds, and on this basis the observed levels of molecular compressibility can be explained.
    Zusätzliches Material: 6 Ill.
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  • 167
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 297-307 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The molecular weight distributions of three polydimethylsiloxanes (PDMS) have been determined by gel-permeation chromatography (GPC), by gas-liquid chromatography (GLC), and by precipitation fractionation. The GPC data are greatly improved by correction for band spreading. For a high molecular weight polymer the corrected distribution agrees closely with the theoretical molecular weight distribution calculated from polymerization kinetics.
    Zusätzliches Material: 7 Ill.
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  • 168
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 429-429 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 169
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 515-524 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: An x-ray study of poly(N-butyl isocyanate) (PBIC) was undertaken with the aim of providing the structural information required for the calculation of its ultraviolet absorption spectrum. Well defined diffraction patterns are obtained from powder samples and oriented films of the polymer cast from cyclohexane solution. All the reflections can be satisfactorily indexed in terms of a pseudo-hexagonal unit cell with a = 13.3 Å and c = 15.4 Å. This indexing and the intensity distribution lead to the conclusion that PBIC has a helical structure with a translation of 1.94 Å and a rotation of 135° per monomeric unit (i.e., the c axis corresponds to 8 units in 3 helical turns). In the absence of single-crystal data on closely similar model compounds, a range of possible bond lengths and angles was assumed. The atomic coordinates of the chromophoric group of PBIC were then computed using the restrictions imposed by the helical parameters. From an investigation of all the assumed range of bond lengths and angles, a few closely similar structures having no unacceptably short van der Waals contacts were found. A comparison of calculated and measured densities indicates that there are two molecules per unit cell. Construction of space-filling models of PBIC supports this conclusion.
    Zusätzliches Material: 3 Ill.
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  • 170
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 563-574 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Solution parameters for the polymer poly-γ-trifluoro-propylmethylsiloxamer has been determined in cyclohexyl acetate, methyl hexanoate, and ethyl acetate. Interpretation of data follows the theory of Fox and Flory. In contrast to poly-dimethylsiloxane, an increased steric hindrance to rotation about the siloxane bond occurs as evidenced by the characteristic ratio of root-mean-square end to end dimensions, (r02/r0f2)1/2, found to be 1.90 and 1.96 at 25.0 and 72.8°C, respectively. This increase is considered to be primarily due to nearest-neighbor interaction of the polar substituent on the silicon atom. The relation, [η]θ ∝ M1/2, was observed to hold for this polymer system. The hydrodynamic model appropriate for the polymer is a random coil considerably more permeable to solvent flow than is generally reported for linear polymers. The universal parameter φ was determined to be 1.5 × 1021. The effect of temperature on polymer configuration is indicated to be negligible.
    Zusätzliches Material: 5 Ill.
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  • 171
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 725-733 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The site of chain scission and crosslinking in vulcanized natural rubber irradiated with 4 MeV electrons has been determined by analysis of stress relaxation data. Sulfur and peroxide vulcanizates of different crosslink densities were prepared and the crosslink densities determined from stress-strain measurements. Stress relaxation was measured during irradiation using modified commercial relaxometers. The specimens were maintained in an atmosphere of nitrogen to minimize oxidative side effects. Scission is deduced to take place in the vicinity of crosslinks, since the rate of continuous stress relaxation is independent of crosslink density. Scission may be associated both with crosslinks initially present and with those subsequently introduced by irradiation. Crosslinking by radiation is largely a random process. However, there is a crosslinking reaction dependent to a slight extent on crosslink density as well as a small contribution from random scission reactions. G values for the random reactions are given.
    Zusätzliches Material: 6 Ill.
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  • 172
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 897-907 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly-ε-caprolactone prepared by a dibutylzinc-catalyzed bulk polymerization process was fractionated, and the solution properties of the fractions were studied in benzene and in dimethylformamide. In these solvents at 30°C the Mark-Houwink relations were [η] = 9.94 × 10-5 Mw0.82 and [η] = 1.91 × 10-4 Mw0.73, respectively. The value of KΘ was found to vary from 1.1 to 1.2 × 10-3 when determined by three known extrapolation techniques. Poly-ε-caprolactone chains appear to be quite flexible in solution, and the steric hindrance parameter σ had the low value of 1.37. Root-mean-square end-to-end dimensions were approximated from the experimental data and calculated from the Debye-Bueche and the Kirkwood-Riseman theories.
    Zusätzliches Material: 5 Ill.
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  • 173
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 983-992 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Interferometric studies have been made on cotton fibers as well as on twisted nylon filaments. The results so obtained provide strong evidence that the fibrils in the cotton fiber become less inclined to the fiber axis as one proceeds from the surface to the core. Also, studies on twisted nylon filaments by the fiber refractometer and Becke line techniques indicate that the latter, as practiced in this laboratory, does give values of refractive index which are heavily weighted towards the fiber periphery.
    Zusätzliches Material: 3 Ill.
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  • 174
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1085-1099 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Measurements of infrared absorbance as a function of temperature down to 77°K have been made on poly(ethylene terephthalate). Transitions observed by other techniques such as torsion pendulum measurements are reflected in the infrared measurements by an abrupt change in the slope of the absorbance versus temperature. The infrared measurements are made on bands of known structural origin so the structures contributing to each transition can be determined. The β transition is shown by infrared to be a composite of two peaks with the lower-temperature portion arising from the amorphous regions and the higher-temperature portion from the crystalline regions.
    Zusätzliches Material: 8 Ill.
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  • 175
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1119-1121 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
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  • 176
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1123-1150 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Stress, strain, and birefringence measurements have been carried out on swollen and unswollen networks of ′cis-1,4-polybutadiene polymers. Neither stress-strain nor birefringence-strain relations of unswollen specimens obey the Gaussian network theory, but both can be fitted by the Mooney-Rivlin equation. On the contrary, data on specimens swollen in tetralin, decalin, benzene, and carbon tetrachloride strictly obey the Gaussian network theory. Existing methods for evaluating the temperature coefficient of the unperturbed dimensions, d In 〈r2〉/dT, from the stress-temperature relation are applied to the present data and discussed in some detail. It is concluded that reliable values of d In 〈r2〉/dT are not obtainable from data on unswollen samples because of the pronounced non-Gaussian effect. The value 7.5 Å3 for the optical anisotropy Å3 (an alternative to the stress-optical coefficient) for unswollen specimens is markedly larger than values (5.8 Å3 on the average) for swollen specimens. This is interpreted as due to the shortrange orientational order among polymer segments. The quantities 〈r2〉, ΔΓ, and their temperature coefficients are calculated for both cis-1,4-polybutadiene and cis-1,4-polyisoprene chains, on the basis of the rotational isomeric state approximation for bond rotations. Values of ΔΓ for cis-1,4-polybutadiene calculated using Clément and Bothorel's set of anisotropic bond polarizabilities are in good agreement with observed values for swollen specimens. Those for cis-1,4-polyisoprene obtained using the same set of anisotropic bond polarizabilities are somewhat smaller than observed values for unswollen specimens. This departure is in the direction expected from the behavior of ΔΓ upon swelling (i.e., a decrease in ΔΓ upon swelling).
    Zusätzliches Material: 10 Ill.
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  • 177
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1281-1282 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 178
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1357-1366 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Three types of commercial styrene-acrylonitrile copolymer were fractionated by coacervate extraction and by column-elution techniques. Both methods were studied with two different solvent-nonsolvent pairs. Glass wool was used as the support material in the column. Fractionation by the coacervate extraction method was studied with benzene-triethylene glycol as a solvent-nonsolvent system at 60°C and with dichloromethane-triethylene glycol at 25°C. Column elution was carried out with acetone-methanol as the solvent-nonsolvent system at 30°C, and with dichloromethane-methanol at 20°C. Results of excellent reproducibility were obtained by these two methods. Characterization of fractions involved determination of both the molecular weight and chemical composition. It was established that the fractionation of the samples tested was dependent upon molecular weight only. The two methods described above are compared. Each gives an efficient procedure for fractionation of styrene-acrylonitrile copolymers.
    Zusätzliches Material: 6 Ill.
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  • 179
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 127-138 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 2,5-Dichlorothiophene was polymerized to a solid in 93% yield on treatment with aluminum chloride-cupric chloride in carbon disulfide under mild conditions. The product is believed to be poly-5-chloro-2,3-thienylene on the basis of elemental analysis and infrared and NMR spectral data. Hydrogen chloride was collected in 90% of the theoretical amount. Dimer- and tetramer-type fractions were isolated from the polymer. 2,3,5-Trichlorothiophene underwent an analogous transformation in trichlorobenzene at 90-100°C. Polythienylenes coupled through the 2,3-positions have not been reported previously. The net effect of the reaction is nuclear coupling by dehydrohalogenation. We believe that the mechanism involves cationic polymerization accompanied by loss of hydrogen chloride. 2-Chlorothiophene and thiophene gave products of complex make-up.
    Zusätzliches Material: 3 Ill.
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  • 180
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 201-208 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The unit cell dimensions of isotactic polyvinylcyclopropane were determined, based on crystalline, oriented fiber and film samples. Two structures were found: (1) a hexagonal structure with a = 13.6 Å, c = 6.48 Å, 31 helix, space group P31 and P32, ρ(calc) = 0.9805 g/cm3, ρ(obs) = 0.975 g/cm3; (2) a tetragonal structure with a = 15.21 Å, c = 20.85 Å, 103 helix, space group I4, ρ(calc) = 0.926 g/cm3.
    Zusätzliches Material: 4 Ill.
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  • 181
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 269-281 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The polymerization of styrene initiated by 2,2′-azobisisobutyronitrile has been studied in N,N-dimethylformamide solution at 60°C in the presence of hexakis(N,N-dimethylformamide) iron(III) tetrafluoroborate alone, and also in the presence of added lithium chloride. The presence of Fe(DMF)63+ ions in the polymerizing systems caused retardation, but iron(III) chloro complexes produced well defined inhibition periods. Velocity constants at 60°C for polystyryl radicals towards Fe(DMF)63+, Fe(DMF)5Cl2+, Fe(DMF)4Cl2+, and FeCl4- ions were calculated to be 847, 4.15 × 104, 6.55 × 104, and 3.14 × 104 l./mole-sec, respectively. Values of the initiator efficiency f for most systems investigated ranged from 0.59 to 0.62.
    Zusätzliches Material: 6 Ill.
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  • 182
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 321-332 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A series of aromatic polyimide-co-amides of high thermal stability were synthesized. Low-temperature solution condensation involving aromatic diamines of varying basicity and bifunctional carboxylic acid chlorides containing performed imide rings was empolyed. This approach offers several advantages over the conventional polyamic acid route. The final polymers obtained are linear, soluble, and of high molecular weight. Solution of the final polymers are stable in contrast to polyamic acid solutions, which depolymerize hydrolytically due to the neighboring-group effect. Tough, flexible films were cast from solution and required no heat cure. The properties of one polymer made by the preformed ring approach were compared to its structurally related amide and imide homologs.
    Zusätzliches Material: 4 Ill.
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  • 183
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 363-377 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The thermal degradation of poly(2,6-dimethyl-1,4-phenylene ether) has been investigated to 1000°C in an inert atmosphere. X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry were employed to study the physical changes in the polymer, and vapor-phase chromatography, infrared spectroscopy, and mass spectrometric thermal analysis were used to elucidate the chemical aspects of the degradation process. It was found that degradation occurs in two steps: (1) a rapid exothermic process occurs between 430 and 500°C, leading to the evolution of phenolic products, water, and a black, highly crosslinked residue, and (2) a slower, char-forming process occurs above 500°C, characterized by the evolution of methane, carbon monoxide, and hydrogen. The chars formed in process 2 were found by x-ray analysis to be amorphous. The infrared spectrum of a sample heated to 510°C is nearly identical with that of the starting polymer, indicating that oxidative reactions are not important in the first process. The data for the low-temperature process are consistent with a thermal degradation scheme based on the radical-redistribution reaction of polyphenylene ethers and/or the degradation of o-benzylphenols formed by the thermal rearrangement of o-methyl diphenyl ethers. The char-forming process is best explained by simultaneous operation of the Szwarc mechanism of toluene pyrolysis, producing hydrogen and methane and reactions that cleave the aromatic rings and produce carbon monoxide.
    Zusätzliches Material: 6 Ill.
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  • 184
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 157-172 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Self-protective polyesters were synthesized in two ways: by polymer analog transformations on polymers obtained and by introduction of inhibiting groups into the polymer during synthesis. It is shown that the Fries rearrangement takes place in the aromatic polyesters in the presence of the Friedel-Crafts catalysts and on ultraviolet irradiation as well. Thermogravimetric analysis of the rearranged polymers and investigations of the influence of the ultraviolet irradiation on their properties show that the rearrangement markedly increases the photochemical and thermal stability of the polymers. Photostabilization may also be accomplished by the introduction of inhibiting groups, such as hydroxyl, sulfur, or phosphorus into the polymer molecule.
    Zusätzliches Material: 9 Ill.
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  • 185
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 183-199 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The γ-ray copolymerization of carbon monoxide with cyclic ethers, such as ethylene oxide, phenyl glycidyl ether, 1,3-dioxolane, 2-vinyl-1,3-dioxolane, terahydrofuran, 1,4-dioxane, and acetaldehyde was studied. A yellowish or brownish powdery copolymer was obtained in most of the cases examined. The infrared spectra showed that copolymers containing the ester structural unit were produced in the copolymerization with cyclic ethers which have no vinyl groups, and that a copolymer containing a ketone structure was produced from cyclic ether having vinyl group. It was found that the copolymer with ethylene oxide also had a β-propiolactone ring structure at the chain end or the side chain. The copolymers were confirmed to be partially crystalline from the x-ray diffraction diagrams. Further, a ring-opening polymerizability of the cyclic ether by γ-radiation was discussed. And it was found that as the bond dissociation energy between the carbon-oxygen linkage of the cyclic ether is small, the polymer yield both in the homopolymerization and copolymerization with carbon monoxide is high. A mechanism for the copolymerization is proposed on the basis of the results.
    Zusätzliches Material: 7 Ill.
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  • 186
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 283-296 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ordered heterocycle copolymers of high thermal stability were prepared from aromatic dianhydrides reacted with aromatic diamines containing preformed benzoxazole or benzothiazole units. These ordered benzoxazole-imide and benzothiazole-imide copolymers were prepared in the form of their soluble precursor polyamic-acids, which, after fabrication to desired shapes, were converted to the thermally stable polymer. In general, these polymers are more resistant to air oxidation at elevated temperatures than are simple aromatic polyimides, and their thermoöxidative stability is equal to or greater than that reported for benzoxazole or benzothiazole homopolymers. Unlike the o-hydroxyamide precursors to simple polybenzoxazoles, the amic acid precursors to benzoxazole-imide ordered copolymers do not require temperatures above 300°C to complete ring closure nor inert atmospheres to prevent polymer degradation during ring formation. Excellent self-supporting films and film coatings for metals were prepared. Selected compositions were readily spun to excellent fiber.
    Zusätzliches Material: 4 Ill.
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  • 187
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 333-349 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Poly-2,6-dimethoxystyrene (P26) was used as the polymeric backbone and was obtained by a new synthetic route involving the Wittig reaction. The grafting reaction was studied by polymerizing styrene with stannic chloride as catalyst in the presence of various concentrations of preformed P26 in solution with carbon tetrachloride and nitrobenzene at 60, 45, 30, and 0°C. The product was fractionated with cyclohexane and the fractions were analyzed by ultraviolet absorption spectroscopy and density-gradient ultracentrifugation. The molecular termination constant of P26 at 30°C was 0.106 much larger than the value of 0.016 which had been obtained for poly-p-methoxystyrene at 0°C. The amount of grafting and grafting efficiency generally increased with increasing temperature, contrary to results using the cationic initiation reaction. Anomalous results were obtained at 0°C as the product was no longer completely soluble. The ratio of grafted to ungrafted polystyrene chains was proportional to the concentration of P26 and generally increased with temperature. The grafting reaction was competitive with the normal termination reaction, and the energy of activation of the grafting reaction was estimated to be larger by ca. 7 kcal/mole.
    Zusätzliches Material: 4 Ill.
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  • 188
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 351-362 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The terpolymerization of carbon monoxide, aziridines, and cyclic ethers was carried out by γ-irradiation. A partially crystalline solid copolymer was obtained. The infrared spectrum of the copolymer obtained indicated characteristic peaks due to the secondary amide and ester groups. The results of elementry analysis, infrared spectra, and x-ray diffraction of the copolymer showed that terpolymerization of carbon monoxide, aziridine, and cyclic ether took place by γ-irradiation. 2-Vinyl-1,3-dioxolane was polymerized in the system of carbon monoxide and ethylenimine to give a solid polymer. The infrared spectrum showed characteristics of the secondary amide and dioxolane ring, while no absorption due to carbonyl group of ester was observed. The infrared spectra and results of elementary analysis confirmed that the terpolymerization of carbon monoxide-ethylenimine-2-vinyl-1,3-dioxolane occurred.
    Zusätzliches Material: 9 Ill.
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  • 189
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 409-413 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 190
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 1-2 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 191
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 35-46 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The syntheses of N,N′-divinylureas and some related compounds are reported. Polymerization of these monomers and determination of the structures of the resulting polymers are described. Evidence is presented which supports the tendency of vinylureas to react through their tautomeric form.
    Zusätzliches Material: 1 Tab.
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  • 192
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 55-72 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: New, bifunctional, bridgehead-substituted triptycenes were synthesized and used to prepare a series of triptycene polymers, including polyesters, polyamides, polyurethanes, and a polyoxadiazole. Certain of these partially aliphatic polymers were thermally stable. Clear and colorless films were obtained in some instances.
    Zusätzliches Material: 1 Ill.
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  • 193
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 111-125 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The polymerization of toluene with aluminum chloride and cupric chloride was performed in carbon disulfide and in a neat system. The solvent reaction produced an insoluble, light-brown product which did not melt below 350°C. In the neat system, polymerization was much more vigorous, yielding a dark, purple-brown solid with mp ∼250°C and molecular weight of 634. Infrared, NMR, and ultraviolet spectroscopy, along with elemental analysis and oxidative degradation, indicated that the backbone chain contains o-polyphenylene units with the methyl group situated in the 4-position. Some p-polyphenylene structures may also be present. Evidence for small amounts of benzyl and polynuclear moieties was obtained. The mechanistic aspects are discussed. Our principal conclusions concerning oligomer structure are in disagreement with those of Kuwata.
    Zusätzliches Material: 8 Ill.
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  • 194
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 173-181 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Trialkylboron-oxygen, an active, low-temperature free-radical initiator, has been employed to investigate the effects of very low temperatures on the copolymerizations of vinyl acetate with cis and trans-1,2-dichloroethylenes. The low temperatures favor the propagation rate relative to the transfer rate, such that high molecular weight copolymers containing substantial quantities of 1,2-dichloroethylene can be prepared. The molecular weights of the copolymers depend only on the amounts of 1,2-dichloroethylene in the copolymers, regardless of the isomer which takes part in the copolymerization. Since the double bond of the trans isomer is about six times as reactive as that of the cis isomer, this indicates that the dominating chain transfer reaction occurs by chlorine atom elimination subsequent to the addition of the dichloroethylene unit to the growing free radical chain. It is suggested that a similar chain-transfer mechanism occurs in the polymerization of vinyl chloride, wherein an infrequent head-to-head placement of monomer unit is followed by ejection of a chlorine atom to form an olefinic bond and termination of that growing chain. The presence of the 1,2-dichloroethylene unit in the copolymer increases the glass transition temperature approximately 1°C per weight per cent copolymerized with the vinyl acetate.
    Zusätzliches Material: 4 Ill.
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  • 195
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    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 217-235 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Several α-olefins containing the trifluoromethyl group were prepared and characterized. 4,4,4-Trifluoro-1-butene, 3-trifluoromethyl-1-butene, 5,5,5-trifluoro-1-pentene, and 4-trifluoromethyl-1-pentene were homopolymerized with VCl3-Al(i-Bu)3 catalyst. The trifluorobutenes gave low-melting polymers with low fluorine contents. Polymers obtained from the trifluoropentenes were soluble having moderately high intrinsic viscosities. Copolymerizations of these monomers with their nonfluorinated homologs by the same catalyst system indicated low reactivities of the fluoromonomers. Nuclear magnetic resonance spectra of the fluorinated and nonfluorinated monomers and their respective spectroscopic studies with the catalyst (C5H5)2TiCl2-Al(CH3)3 indicated an electron deficiency of the vinyl group of the fluorobutenes. This was related to the inductive effect of the trifluoromethyl group. The inductive effect of this group was absent in the fluoropentenes and the nonfluorinated monomers. The electron-deficient vinyl group of the fluorobutenes apparently did not allow these monomers to coordinate with the active sites of the catalyst. Polymerization studies of the nonfluorinated monomers, 1-butene, 3-methyl-1-butene, 1-pentane, and 4-methyl-1-pentene, with the catalyst VCl3-Al(Bu)3, were performed in the presence of compounds containing the trifluoromethyl group. Results indicated that this group did not retard the rate of polymerization of these monomers. Evidence is presented to show that a catalytic amount of benzotrifluoride enhanced the rate of polymerization of α-olefins, particularly that of sterically hindered monomers such as 3-methyl-1-butene.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 196
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 237-245 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The photo-oxidation of PVC and its model compounds, the dl- and meso-2,4-dichloropentanes, were studied by high-resolution NMR spectroscopy. The structure, —CHCl—CH2—CO—CH2— was found to be present in PVC after photo-oxidation. Two peaks, which corresponded to the CHCl and CH2 groups next to the carbonyl group, were observed in carbon disulfide-acetone-d5 mixture, at 6.15 and 7.25τ, respectively. From the NMR spectra, the ratio of the CH2 to CHCl protons in PVC and the model compounds were found to increase linearly with the time of photo-oxidation after induction periods. The initial rates of the model compounds were comparable with that of PVC; i.e., 1.6 × 10-2 hr-1, at 30°C. Since similar gaseous products were also detected by mass spectrometry in the initial stage, their photo-oxidation probably assumed the same rate-determining step. According to the results that the dl-2,4-dichloropentane was photo-oxidized 1.5 times faster than the meso-compound, it would be likely that the syndiotactic sequences in PVC might be more easily photo-oxidized than the isotactic sequences.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 197
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 259-264 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Poly(vinyl 2-furylacrylate), a new photosensitive polymer, was prepared, and its photosensitivity was investigated. The polymer cannot be synthesized by the usual procedure, condensation of poly(vinyl alcohol) and 2-furylacrylyl chloride in hot pyridine, but is easily prepared by the aqueous alkaline process, regardless of the degree of polymerization. Poly(vinyl 2-furylacrylate) is remarkably highly photosensitive and is spectrally sensitized by aromatic nitro compounds and aromatic carbonyl compounds. The mechanism of photochemical reaction is considered to involve the dimerization of the furylacrylyl group, and the quantum yield appears to be constant.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 198
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 265-268 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate of tri-o-tolyphosphine-initiated photopolymerization of methyl methacrylate was found to be significantly higher than that for the triphenylphosphine initiated polymerization. The mechanism was shown to be dependent upon the concentration of the initiator. At low concentrations (10-4 mole/l.), an activated complex is the initiating species, while at higher concentrations (above 10-2 mole/l.) homolytic cleavage of the phosphorus-carbon bond is the radical source. Steric inhibition of resonance is advanced as an explanation for the enhanced activity of tri-o-tolylphosphine over triphenylphosphine.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 199
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The chemistry of the titanium(III) chloride(AA)-ethylaluminum dichloride-tetrakis-(dimethylamino)silane system for the polymerization of propylene was studied. A complex of ethylaluminum dichloride with tetrakis(dimethylamino)silane was isolated. It was shown that this complex contains ethylaluminum dichloride and tetrakis(dimethylamino)silane in the ratio of 2:1. This complex with titanium(III) chloride is responsible for the polymerization activity.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 200
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 7 (1969), S. 379-385 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The cupric sulfate-hydrazine system has been used to initiate the aqueous solution polymerization of methyl methacrylate at pH 9.25 in the presence of oxygen. At cupric sulfate concentrations greater than the saturation solubility of cupric hydroxide, hydrazine is adsorbed on, and decomposes on, the surface of the hydroxide. The kinetics of the decomposition are zero-order both in the absence and the presence of monomer. The initiation of the polymerization occurs both at the surface of the cupric hydroxide on to which some monomer is adsorbed and also in solution. Below the saturation solubility of cupric hydroxide, the initiation reaction between cupric ions and hydrazine occurs in solution.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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