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  • Polymer and Materials Science  (11)
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  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Kristallisiert man unter Kompression in einer Richtung einen Film aus schwach vernetztem Polyäthylen, so entstehen in den kristallinen Bereichen einzigartige Kettenorientierungen. Zunächst erfolgt dabei bei relativ geringer Kompression die Orientierung der zur Filmoberfläche parallelen (200)-Kristallebene, danach bei erhöhter Kompression diejenige der (110)-Ebene.Die Dichte der Elementarzelle liegt nahe eins, und die kristallinen Bereiche sind sehr groß, obwohl der Film sehr rasch aus der Schmelze erhalten wurde. Parallel zur Filmoberfläche sind die Kristallite größer als 1500 Å, senkrecht dazu im Bereich 170 - 350 Å. Hieraus und aus zusätzlichen elektronenmikroskopischen Untersuchungen kann man schließen, daß bei solchen Filmen ein neuer Typ lamellarer Struktur vorliegt. Er unterscheidet sich bezüglich der molekularen Ausrichtung erheblich von dem Typ, den man beim Kristallisieren von Polyäthylen unter isotropen Bedingungen erhält.
    Notes: If lightly cross-linked polyethylene films are crystallized from the melt under uniaxial compression, a very unique alignment of the molecular chains in the crystalline phase of the samples appears. The orientation of crystallites in which the (200) crystal plane is located parallel to the film surface first appears at a relatively low degree of compression, and subsequently the orientation in which the (110) crystal plane is located parallel to the film surface follows at higher degrees of compression.Despite the fact that the samples were crystallized from the melt rather rapidly, the unitcell density of the crystalline phase was very close to unity and the size of crystallites was very large. The dimensions of crystallites in the direction perpendicular to the film surface were in a range of 170 - 350 Å but they were as large as more than 1500 Å in the direction parallel to the film surface. Thus it is confirmed in addition by electron microscopic observation that these samples have a new type of lamellar structure in which the molecular alignments are quite different from those for the so-called lamellar structure for polyethylene crystallized under isotropic conditions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1377-1387 
    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 molecular orientation of stretched polyethylene has been estimated separately for the crystalline and amorphous phases by using x-ray and birefringence techniques. It is confirmed that if a hightly crosslinked polyethylene is highly stretched rapidly in the perfectly molten state and cooled to room temperature, a fibrous structure comprised of highly oriented crystallites and almost unoriented relaxed amorphous chains is produced. Some properties such as dynamic mechanical properties and thermodynamic property are discussed in relation to the molecular structure.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 21 (1977), S. 2125-2134 
    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: Some physical and chemical properties of an ionic complex made from the weak polyelectrolytes carboxymethylated poly(vinyl alcohol) (PA) and aminoacetalized poly(vinyl alcohol) (PC) are investigated in comparison with those of another ionic complex made from the strong polyelectrolytes sulfated poly(vinyl alcohol) (PSA) and poly(vinyl alcohol) acetalized with diethoxyethyltrimethylammonium (PTC). It was found that when the complex PC-PA was heated at high temperatures, covalent amide bonding took place, whereas no significant change occurred in the case of the PTC-PSA complex. As a result of these structural changes, the degree of swelling of the PC-PA complex in water was markedly decreased, but that of the PTC-PSA complex was not changed by the treatment. The PC-PA complex was insoluble in water and in 1N HCI and 1N NaOH aqueous solutions even if not heat treated, but the PTC-PSA complex was soluble in such acidic and basic aqueous solutions but not in water if heat treated. The PC-PA and PTC-PSA films exhibited good mechanical properties.
    Additional Material: 3 Ill.
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  • 4
    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: Improvements in physical properties of polyvinyl alcohol fibers were attempted by means of both crosslinking and graft copolymerization. By using the ceric iron redox system on synthetic fibers spun from polymer blends containing polyvinyl alcohol (PVA) and its partially (about 15 mole-%) N-methylolcarbamoylethylated products (PVM) in which the blend ratios were 0/100, 10/90, 15/85, and 20/80 by weight, methyl methacrylate (MMA) was grafted at 30°C. in the aldehyde-free acetone-water system after crosslinking by heat treatment or successive acid treatment. Grafting increases with increasing PVM component. This may be ascribed to the coarsening of the fiber texture caused by polymer blending and the increasing of methylol groups as a reducing agent. Moisture regains decrease with increasing graft fraction, but these appear to be greater than the additive values of backbone and graft polymer. Less shrinkage in boiling water is obtained with the increase of PVM component and grafting; the decreased shrinkage is significant in the acid-treated PVM-PVA fibers, and it reaches a nearly sufficient value at about 50% graft-on. The PVA fibers do not give sufficient shrink-proofing. The inherent tenacity and elongation of the grafted fibers increase slightly with increasing graft-on or denier except at the high grafting above about 100, 150, and 300 in the PVA, acid-treated, and acid-untreated PVM/PVA fibers, respectively; whereas the tensile strength in grams/denier decreases with grafting. Although at high grafting, a destruction in the fiber texture will perhaps occur, the coarser the texture of backbone fiber, the harder the change by grafting. The knot/normal ratios in tensile strength or elongation of the grafted fibers have been retained at above 90%. The elastic recovery of the grafted fibers is considerably improved as compared to the conventional Vinylon fibers. The improvements in the acid-treated and grafted PVM/PVA (20/80) fibers are significantly greater above and below 50% graft-on, especially in the range of lower extension. As expected, the thermosetting property is also appreciably imparted with grafting. In the conventional Vinylon fibers, the formalization for shrink-proofing is usually at a sacrifice of elastic recovery. But MMA grafting in the PVM/PVA fibers gives a fairly good elastic recovery and less shrinkage in addition to thermosetting property, making the most of the characteristics in the longer intermolecular crosslinkages formed between methylol groups or PVA-OH groups and methylol groups.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2741-2751 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: H-type crosslinking and Y-type long-chain branching have been examined for linear polyethylene samples irradiate at different temperatures with 60Co gamma rays in vacuum by solution-state 13C-NMR spectroscopy. In this study, relatively low molecular weight samples were irradiated with doses less than a gel dose in both solid and molten states. Resonance lines associated with H-links and Y-branches have clearly been observed for each irradiated sample and their radiation yields significantly depend on the irradiation temperature and the morphology of the samples. In particular, the G-value for the production of Y-branches is higher than that for H-links at lower temperatures, while the latter is superior to the former at higher temperatures. This may be due to the decrease in the concentration of the primary radicals, which are formed by main-chain scissions and associated with the production of Y-branches, by the recombination with small fragments at higher temperatures. The radiation yields of methyl branches and double bonds are also briefly discussed.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 41 (1990), S. 783-791 
    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 phase transition from cellulose to alkali cellulose (Na-Cell) and the phase structure of Na-Cell have been investigated by CP/MAS 13CNMR spectroscopy. It has been found from the 13CNMR spectra that both crystalline and noncrystalline components of cellulose decrease in resonance intensities in the transition process from cellulose to Na-Cell I, suggesting that the noncrystalline and the crystalline regions of cellulose are converted to Na-Cell simultaneously. The conversion model is considered as follows: The crystalline part imposes some restriction on the swelling of the noncrystalline part of cellulose, but the conversion of both parts to Na-Cell may be possible when the swelling prevails in the whole microfibril as a result of the penetration of the alkaline solution into the crystalline part. Secondly, the 13C spin-lattice relaxation times (T1) have been measured to elucidate the phase structure of Na-Cell. Though two T1 values are obtained for each carbon of Na-Cell except for C6 carbon, Na-Cell has a homogeneous solid structure which is composed of the crystalline regions with a small heterogeneity.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 28 (1990), S. 357-361 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 20 (1976), S. 3365-3374 
    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 crystalline structure of decrystallized cotton, prepared by partial cyanoethylation with the use of sodium hydroxide aqueous solution and acrylonitrile, was examined by x-ray and IR data, in connection with such fabric properties as moisture regain. It was found that the moisture regain of the cotton fabric first increased, passed through a maximum at about 6 mole-% of cyanoethylation, and then slightly decreased with increasing degree of cyanoethylation. The increase of moisture regain in the region of the lower degree of cyanoethylation was well related to the decrease in the crystallinity of cotton. The x-ray diffraction studies revealed that the distension and disorder of the unit cell occurred primarily in the direction perpendicular to the (101) crystal plane as cyanoethylation proceeded.
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1801-1809 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differences in fiber structure between cotton and cuprammonium rayon are studied by a refined broad-line proton NMR analysis of samples swollen with deuterated dimethyl sulfoxide, which has no effect on the spectra but enhances differences in molecular mobility between crystalline and noncrystalline regions. The spectra obtained are decomposed into four components: broad, medium, narrow, and extremely narrow. These components are identified as contributions, respectively, from crystalline and rigid noncrystalline (frozen glassy) material, a noncrystalline glassy component exhibiting local segmental motion, a noncrystalline rubbery component exhibiting liquidlike molecular motion, and protons included in DMSO-d6 as an impurity. The mass fraction of the narrow component in cotton was about 0.01, whereas it was as high as 0.18 in cuprammonium rayon. It is concluded that even in the swollen state, native cellulose is devoid of a liquidlike mobile component, but regenerated cellulose contains a considerable amount of a noncrystalline component involving liquidlike segmental motion of molecules.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 109-120 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Broad-line 1H NMR spectra of linear polyethylene at temperatures in the α-transition range can be analyzed in terms of contributions from the crystalline and noncrystalline components provided molecular motion in the crystalline region is adequately considered. The spectrum of solid n-C32H66 or n-C44H90 prior to melting is used to take account of the contribution of the crystalline region of the polymer to molecular motions. The temperature dependence of the component distribution in the polymer is briefly discussed for a wide range of temperatures, together with previously reported results at low temperatures. The noncrystalline component is in a rigid glassy state at very low temperatures but with rising temperature it transforms to a mobile glassy state with restricted molecular motion, and transforms partially to the rubbery state at high temperature. The crystalline component remains rigid at low temperature, but some molecular motion is associated with it at higher temperatures in the α-transition range.
    Additional Material: 4 Ill.
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