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  • 1960-1964  (6)
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Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 863-863 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 44 (1960), S. 369-381 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilatometers were used to measure the volume-temperature curves of seven poly(4-methyl-1-pentene) (PMP) samples between -30 and +270°C., and to measure crystallization rates on one sample between 220 and 236°C. A glass transition temperature of 18-29°C. was found, and the crystalline melting point was found to be 250°C. The value of dV/dT above and below the glass temperature was used to measure the degree of crystallinity. The results indicate that the crystalline PMP is less dense at room temperature than the amorphous polymer. However, because of different rates of expansion, the normal positive volume change on melting is observed. A density value of 0.828 ± 0.002 g./ml. at 20°C. is calculated for the PMP crystal.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The morphology of two n-alkanes (n-C44H90 and n-C82H166, prepared by E. Stenhagen, et al. ) and linear polyethylenes (Ziegler-type of low and Marlex 50 of high molecular weight, respectively), crystallized from dilute solution by slow cooling, have been studied by electron microscopy and small-angle x-ray scattering. A series of solvents were used with cloud points for polyethylene from about 120°C. (poor solvents, e.g., diphenyl ether) to 65-75°C. (good solvents, e.g., tetrachloroethylene). All samples crystallized with basically the same morphology, showing large, thin flakes or lamellac with the chains perpendicular to the plane of the flakes. This involves chain folding for all polyethylenes studied, as proposed by Keller. In most cases, the large flakes were overgrown with or accompanied by diamond- or lozenge-shaped single crystals (as reported by Jaccodine and Till) containing from 2 to about 20 lamellae and developed as pyramids, sometimes as spirals and sometimes as consecutive layers. Isotactic polypropylene crystallized with a similar morphology. The nucleation and growth mechanisms of the large flakes are not clear. They seem to grow without dislocations, while the diamond-shaped crystals seem to form according to Frank's screw-dislocation growth concepts. Crystallization of polyethylene at high temperatures give thicker lamellae (165 A. at 120°C.) than crystallization at low temperatures (103 A. at 60°C.), as measured by small-angle x-ray scattering, regardless of molecular weight. When heated, the lamellae recrystallized to larger thickness. This would imply that the folding length of the polyethylene chains and the related thickness of stable lamellae are primarily a function of the crystallization temperature. The lamellae of n-alkanes showed a thickness which agreed with the extended chain length of each sample within a few angstroms.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 51 (1961), S. 541-549 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The new alpha olefins 2-allyl-p-xylene, 4-allyl-o-xylene, 5-allyl-m-xylene, 4-(o-tolyl)-1-butene and 4-(p-tolyl)-1-butene were prepared. These olefins, in addition to the known ortho, meta and para allyltoluenes, have polymerized, using aluminum alkyl titanium chloride catalyst, to crystalline polymers. Physical properties of these polymers, both as powder and molded sample, have been studied. Melt temperatures (Tm) and glass transition temperatures (Tg) have been determined using differential thermal analysis, dynamic modulus measurements, and dilatometric measurements; observations on the birefringent melting behavior were also noted. The effects of both olefin chain length and substitution of methyl groups in the ortho, meta, and para position, respectively, on the properties of these polymers have been interpreted according to present concepts. The results are in general agreement with corresponding data for isotactic methyl-substituted polystyrenes. Substitution in the ortho position raises both transition temperatures considerably, while meta and para substitution cause only smaller effects.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose triacetate and triethyl cellulose have been crystallized from dilute solution into regular compact lamellar crystals of microscopic size (10-20 μ) and of the same type as the single crystals previously obtained from linear synthetic polymers The shape of the cellulose acetate crystals (pyramids with square base) conforms with the crystal lattice of cellulose triacetate II (pseudo-orthorhombic unit cell) when the chains are at right angle to the base planes. Compact platelike crystals of pure cellulose containing the lattice of cellulose II (mercerized cellulose) have been prepared from aqueous solutions by slow saponification of water-soluble cellulose acetates. At 90°C. the crystals can be grown to a regular diamond (lozenge) shape (15 × 30 μ in cross section) with a lattice order as good as or better than that of purified dried native cotton fiber or bacterial cellulose. The shape of the crystals conforms with the crystal lattice of cellulose II (monoclinic unit cell with the angle 60°) if the chains are a t right angle to the base planes. It is concluded that the crystals of cellulose and cellulose derivatives are single crystals of a structure analogous to that of synthetic polymers. This would require chain folding also for the cellulose molecules. From studies of molecular models of cellulose chains, a 180° fold is considered possible with about four glucose residues-provided the consecutive units are rotated around the glycosidic bonds.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 545-552 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dilatometric data for the glass transition temperature Tg of poly(4-methyl-1-pentene) (PMP) have been extended to more crystalline samples and rendered more precise. Tg is definitely shown to decrease with increasing degree of crystallinity, an effect which tentatively is related to increasing free volume of the amorphous part of the polymer as the less dense crystalline phase increases and pulls apart the polymer chains in the amorphous regions. Tg is determined to be 14 ± 2°C. for 78% crystalline PMP, and 25 ± 2°C., for amorphous polymer. The existence of a higher-order transition at 125 ± 10°C. is confirmed by x-ray measurements and ascribed to transverse chain segment motion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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