ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles  (48)
  • Physics  (48)
  • AERODYNAMICS
  • ASTRONOMY
  • ENERGY PRODUCTION AND CONVERSION
  • GEOPHYSICS
  • 1980-1984
  • 1975-1979  (48)
  • 1970-1974
  • 1975  (48)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1269-1274 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Earlier work showed that heating causes poly(diethylsiloxane) to undergo a first-order transition from a semicrystalline solid to a more mobile viscous - crystalline material. The latter is composed of two phases and analogies between polymer and liquid crystal morphology and behavior have been made. The viscous - crystalline phase in PDES appears to be unique since the literature is devoid of other documented examples. In this study, spin - lattice and spin - spin relaxation times were measured over a wide temperature range. They show a glass transition at 138°K, a crystal - crystal transition at 206°K, and a transition around 250°K which results from translational motion of the polymer chains with respect to each other. This motion is observed in the amorphous phase at a lower temperature than in the crystalline phase. Translational motion in the crystalline phase is observed on melting of the crystallites. The spin - spin data permitted monitoring of the molecular motions in each phase and the data suggest that these phases exert some influence on the molecular motions of each other. The viscous - crystalline phase in PDES may represent a unique model for studying and understanding “precrystalline” behavior and structure in amorphous solids.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1201-1214 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Experiments were designed to demonstrate that the chemical potential gradient required for liquid transport through swollen network polymer membranes manifests itself as a concentration gradient and that the rate of transport is independent of how this gradient is established. The fluxes of various liquids through a crosslinked rubber membrane were measured in hydraulic and pervaporation modes of permeation. The pressure applied downstream in the latter act simply to fix the activity of the liquid in the downstream membrane surface. The experiments show the flux is a unique function of this activity, and it does not matter how it is established. Sorption data were used to convert these results into a plot of flux versus concentration differential across the membrane which was analyzed by Fick's law using a model for the concentration dependence of the diffusion coefficient. Measured ceiling fluxes for pervaporation for a number of liquids were found to be the same as those estimated from hydraulic permeation data. A simple mathematical representation for an ideal system is used as a pedagogical device to demonstrate the conclusions.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1945-1957 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been presumed in studies of the orientation of low-density polyethylene and its time dependence that the degree of crystallinity remained constant with elongation and did not vary with time following elongation. This paper represents a test of this hypothesis by several methods. The change in crystallinity accompanying stretching has been followed by a modification of an x-ray method for uniaxial orientation proposed by Ruland in which diffraction peaks are resolved into crystalline and amorphous components and their respective areas are determined by two-dimensional integration over both the Bragg angle and the azimuthal angle of diffraction. The weight-fraction crystallinity is then determined from the ratio of the weighted crystalline area to the total area. There appears to be no significant variation in crystallinity up to 50% sample elongation for both slowly and rapidly stretched samples at room temperature. The dynamic crystallinity change accompanying small amplitude vibration has also been determined by the dynamic x-ray diffraction technique and found to be negligible over a wide range of frequency. The degree of crystallinity has also been evaluated from the absolute infrared absorbance of crystallinity-sensitive bands and has also been found to be independent of elongation at room temperature up to 80% elongation. Changes have also been observed by this method during relaxation at constant length following rapid extension and have also been found to be negligible. These results also indicate negligible changes in rotational isomer population. Consequently, we conclude that changes observed during relaxation and vibration arise from orientational changes rather than changes in the degree of crystallinity.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 977-983 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric behavior of poly(diethyl siloxane) supports the adiabatic calorimetric findings of Beatty and Karasz. In particular, a sub-Tg transition is observed near -180°C at 100 Hz, the glass transition near -135°C at 100 Hz, and a first-order transition near -70°C (crystal-crystal transformation). This glass-transition temperature is the lowest reported polymeric glass transition for polymers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1963-1967 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 2551-2570 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Temperature dependence of solute transport through aqueously swollen polymeric films and membranes can be altered to show even apparent negative activation energies by the use of polymers exhibiting a lower consolute behavior in solution. The principles by which we constructed a host of such polymers are discussed. A solubility rule is presented which predicts that solutes in water will show a lower critical solution temperature if the proper hydrophilic-hydrophobic balance is achieved.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 533-566 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The deformation of polyethylene in terms of structural processes has been investigated by low-and wide-angle x-ray diffraction in the case of low-density and, to a lesser extent, high-density polyethylene. The samples possessed a range of simple textures which enabled the deformation processes to be identified. The results are interpreted in terms of a model of stacks of lamellae which have axes along the original draw direction and which deform by lamellar slip, chain slip, and lamellar separation. In most cases these processes accounted for the macroscopic strain but in some cases discrepancies were observed which could be accounted for by inhomogeneous deformation or by the effects of a distribution of lamellar thicknesses. Attempts were made to identify fibrillar slip, without success. The relative contributions of the various deformation processes are examined as a function of temperature and sample treatment by defining a compliance constant for each process. Below room temperature, the results are consistent with expectations based on the α and β mechanical relaxations, whereas the unusual effects at high temperatures are attributed to gradual melting. The compliance constants are also found to depend on the annealing temperature of the sample, and are used to predict the mechanical anisotropy. The volume changes accompanying lamellar separation are examined. They were less than expected in low-density polyethylene, but satisfactory agreement was obtained in high-density polyethylene. A general relation is suggested between volume changes and the lateral development of the lamellae. Hence in narrow lamellae the interlamellar layer can contract laterally whereas the greater constraints imposed by wide lamellae lead to void formation. Other effects examined include the reversibility of the processes which is most marked in the case of chain slip and which is explained by the presence of restoring forces in the amorphous regions including the fold surface. Finally, the differences between low- and highdensity polyethylene are highlighted, emphasizing the part played in the deformation by the amorphous component.
    Additional Material: 23 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Further stress relaxation experiments, mostly at 50°C, are reported on mixtures of crosslinkable ethylene-propylene terpolymer with saturated ethylene-propylene copolymer (molecular weights 3.6 and 45 × 104) containing up to 50% by weight of copolymer, crosslinked by sulfur to leave the saturated copolymer unattached and free to reptate in the copolymer network. Stress relaxation was measured in small simple elongations (stretch ratio about 1.15) on samples which had been extracted to remove a large part of the unattached copolymer and dried. The relative increase in modulus at long times (104 sec) increased with the proportion extracted; at short times (1 sec), extraction of the lower molecular weight copolymer increased the modulus to about the same extent but extraction of the higher molecular weight copolymer affected it very little. The relaxation modulus of the copolymer extracted from sample 50H (50% copolymer of high molecular weight), obtained by difference, agreed with that for the total copolymer except for a small difference probably attributable to molecular weight selectivity in the extraction. Stress relaxation was measured on sample 50H at six higher elongations up to a stretch ratio of 3. The dependence of stress on time and strain was consistent with an analysis based on the following assumptions: (a) linear additivity of the network and unattached copolymer contributions, (b) strain-time factorization of the stress contributions from the individual components, (c) a strain dependence for the unattached component corresponding to the presence of a Mooney-Rivlin C2 term only, (d) a strain dependence for the network component which does not follow the Mooney-Rivlin equation but is dominated by a simple neo-Hookean term.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 703-714 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress relaxation and moduli of elasticity of the composite system crosslinked poly(2-hydroxyethyl methacrylate) (PHEMA)-glass beads were studied dry and swollen in water to equilibrium state over the temperature range 5-170°C. The moduli of the composites in the dry state increased with increasing filler concentration, while those of the composites measured in the swollen state up to the volume concentration of the filler vf′ ≅ 0.15 decreased. In this respect the composites behaved as porous systems, i.e., as polymers with macroscopic defects. This effect was explained as a consequence of weak filler-matrix interaction. The results were compared with the existing theories of moduli of the composite materials.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1159-1166 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fundamental vibrational frequencies of an isolated chain of trans-1,4-polychloroprene have been calculated. The agreement between the calculated and experimentally observed crystalline frequencies supports the molecular model for the structure of trans-1,4-polychloroprene and the force field employed in the calculations. The results of the normal coordinate analysis indicate that there is essentially no coupling between adjacent translational repeat units of trans-1,4-polychloroprene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...