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  • Polymer and Materials Science  (36)
  • Gitterdefekte  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Wachstumsdefekte in polymeren Nadelkristallen (1981)
    Springer
    Colloid & polymer science 259 (1981), S. 241-246 
    Details
    ISSN: 1435-1536
    Keywords: Polystyrol ; Nadelkristalle ; Gitterdefekte
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Summary Lattice defects in polymeric needle crystals (shish) were investigated. The length of the crystals depends on preparation conditions and may vary between 0.1μm and severalμm. Density fluctuations exist along the individual needle crystals. The wave length of the fluctuation is controlled by the chemical nature of the polymer and its amplitude by preparation and annealing conditions. The wave length of the density fluctuations may vary from 90 Å to 300 Å. Needle crystals from isotactic polystyrene additionally exhibit (001) grain boundaries. The orientation relationship of adjacent grains along a needle corresponds to a 180° rotation of the lattice around the molecule axes. The molecular nature of that grain boundary is discussed.
    Notes: Zusammenfassung Die Gitterdefekte in polymeren Nadelkristallen (shish) werden untersucht. Die Länge eines Nadelkristalles kann je nach Herstellungsart.zwischen 0.1μm und mehrerenμm variieren. In den einzelnen Nadelkristallen bilden sich längs der Nadelrichtung Dichteschwankungen aus. Die Schwankungslängen hängen in der Hauptsache von der Polymerart ab, während die Amplituden der Schwankung von der thermischen Vorgeschichte abhängen. Die Schwankungslängen sind zwischen 90 Å und 300 Å. In Nadelkristallen aus isotaktischem Polystyrol sind zusätzlich (001)-Korngrenzen vorhanden. Die Orientierung beider Kristallgitter entspricht einer Rotation von 180° um die Molekülachse. Ursachen für diesen Typ von Korngren zen werden diskutiert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01381767
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  • 2
    Electronic Resource
    Electronic Resource
    Temperature dependence of secondary crystallization in linear polyethylene (1969)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 659-666 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 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.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1969.160070405
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  • 3
    Electronic Resource
    Electronic Resource
    Transient effects in the crystallization of polyethylene (1969)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 821-827 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 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, whereas at larger undercooling, 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 about 5°C below Tp. 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.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1969.160070507
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  • 4
    Electronic Resource
    Electronic Resource
    Lamellar and interlamellar structure in melt-crystallized polyethylene. II. Lamellar spacing, interlamellar thickness, interlamellar density, and stacking disorder (1971)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 85-114 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the small-angle scattering power and the degree of crystallinity in melt-crystallized high-density polyethylene have been used to evaluate the “amorphous” density in situ by the relation, \documentclass{article}\pagestyle{empty}\begin{document}$ (2\pi/V)\int_0^\infty {S\tilde g} (S)dS = (\rho_{\rm c} - \rho_{\rm a})^2 \upsilon_{{\rm er}} (1 - \upsilon_{{\rm er}}) $\end{document} where V is the irradiated volume and ḡ(S) is the “slit-smeared” absolute intensity. The amorphous density is a function of sample history and is always higher than the extrapolated melt density. After slit-height correction, and within the experimental error, the ratio of the two observed long periods is 2:1 at all temperatures (25--126°C). The lamellar thickness and the average interlamellar spacing are obtained from the degree of crystallinity and the first corrected long period. At increasing temperatures between 25°C and 110°C, the lamellae become thinner while the interlamellar zone expands by almost half. Over this range the changes are reversible with temperature. Above 110°C, both the lamellae and the interlamellar region expand with temperature. The thickening is partially reversible upon recooling. Other results obtained include measurements of stacking disorder and of microstructural changes with crystallization temperature and with time at ambient temperature.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1971.160090107
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  • 5
    Electronic Resource
    Electronic Resource
    Rapid measurements of elastic modulus and density in polypropylene sheet during aging (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 1579-1584 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: New methods for rapidly obtaining elastic modulus and density measurements during isothermal polymer aging are given. The elastic measurements are performed using a Rockwell hardness tester. In this case, the elastic recovery is measured. Rapid density measurements are performed using a “double drop” density gradient columan method. Here, a fully aged and a freshly quenched specimen are dropped simultaneously into the column. Simultaneous column height differences directly measure the density difference of the two specimens. The results of these two experiments extend previously reported aging measurements to relatively low times of aging. A log (time) law for both properties is found to the smallest times measured.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260513
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  • 6
    Electronic Resource
    Electronic Resource
    Cold-drawing behavior of naturally aged poly(ethylene terephthalate) (1986)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 1631-1643 
    Details
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The cold-drawing behavior of naturally aged poly(ethylene terephthalate) (PET) is investigated and an attempt is made to compare the mechanical behavior of unaged commercial PET and material which has been naturally aged for 11 years. Mechanical, viscometric, DSC and IR measurements are applied. The previously observed unusual ability of fresh PET bristles to be cold drawn up to 15:1 is not achieved for the naturally aged material. This fact is related to chemical cross-linking occurring on the surface of bristles after drawing and thermal treatment. The cross-linked skin is unsoluble, infusible, and uncrystallizable. The natural aging defeats the ability of PET to respond to external treatments which would otherwise change the internal structure. Such a “stabilization” of material properties is a result of the transformation, during natural aging, of the original physical network into a chemical network consisting of covalent bonds.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1986.070310609
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  • 7
    Electronic Resource
    Electronic Resource
    Kinetics of fiber heat treatment. II. Poly(ethylene terephthalate) fibers (1986)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2591-2616 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Microstructural changes occurring during the process of crystallization in as-spun poly(ethylene terephthalate) (PET) have been monitored using wide- and small-angle X-ray scattering, optical birefringence, shrinkage measurements, and specific gravity.Shrinkage and birefringence results show a competition between two processes: chain re-coiling on the one hand and crystallization on the other hand. A consistent correlation among WAXS, SAXS, shrinkage, and birefringence results is demonstrated. SAXS data show a fibrillar morphology. On the basis of WAXS results, the crystallization is envisioned as a two stage process: first, the formation of defective fibrils, and then the formation of more perfect crystals. WAXS results also demonstrate a remelting phenomenon in samples which have experienced positive shrinking.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1986.090241201
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  • 8
    Electronic Resource
    Electronic Resource
    Kinetics of fiber heat treatment. III Poly(butylene terephthalate) fibers (1986)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 2617-2630 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small- and wide-angle X-ray scattering (SAXS and WAXS), shrinkage, and density experiments were performed on poly(butylene terephthalate) fibers which had been isothermally crystallized at different temperatures, and at constant tension, for times ranging from 100 to 1050 ms.A consistent correlation among WAXS, SAXS, and the kinetic results is demonstrated. Shrinkage results show that the crystallization process prevails over the chain-re-coiling process. Density measurements show that the rate of crystallization increases with temperature. Pinhole X-ray photos show that the orientation of the chains within the crystals remains constant with time and temperature. WAXS diffractometer scans show the development of wide-angle Bragg peaks.SAXS shows the development of small-angle Bragg peaks, as the annealing time is increased. The two-lobe arced pattern is the characteristic pattern. The value for long spacing ranged from 100 to 120 Å, increasing with temperature.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1986.090241202
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  • 9
    Electronic Resource
    Electronic Resource
    RHEED investigation of thin tin films on polypropyleneWork supported by the U.S. National Science Foundation, under Grant No. INT-8206731 and by the Bulgarian State Committee on Scientific and Technological Progress. (1987)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 185-193 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thin layers of (25-1000 Å) tin were evaporated onto a highly oriented polypropylene sheet. Two rates of deposition were used: 5 and 20 Å/s. For the more rapid deposition rate, a preferred orientation of tin was found in all cases. Here, the Sn a axis lay parallel to the polymer chain (polymer c axis). The same orientation relationship was found for the slower deposition rate, but only at lower Sn film thicknesses; at the higher film thicknesses, a random orientation of crystallites is found. Scanning electron micrographs show an equiaxed tin grain structure for the case of no preferred orientation and a platelet morphology for the case of preferred orientation, the thin dimension of the platelets lying perpendicular to the polymer chain axis. Although no clearcut evidence either for or against crystallographic epitaxy has been found, a plausible case for geometrical epitaxy is presented.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1987.090250114
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  • 10
    Electronic Resource
    Electronic Resource
    Confinement orientation (1992)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 785-786 
    Details
    ISSN: 0887-6266
    Keywords: crystal orientation induced by confinement ; polypropylene, confinement orientation of ; poly(ethylene oxide) confinement orientation of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1992.090300717
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