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  • Articles  (218)
  • Polymer and Materials Science  (184)
  • Life and Medical Sciences  (28)
  • Computational Chemistry and Molecular Modeling  (6)
  • ASTROPHYSICS
  • 1980-1984
  • 1970-1974  (206)
  • 1940-1944  (12)
  • 1972  (206)
  • 1944  (12)
Collection
  • Articles  (218)
Keywords
Publisher
Years
  • 1980-1984
  • 1970-1974  (206)
  • 1940-1944  (12)
Year
  • 11
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1811-1836 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model for the crystallization kinetics of polymers is outlined and is used to interpret observations of the crystallization of polyethylene at high pressures. This model introduces a distinction between σe the lamellar surface energy which controls the lamellar thickness, and σe′, the surface nucleus surface energy which controls the growth rate. Differential scanning calorimetry and electron microscopy data for several polyethylenes crystallized at pressures of up to 8 kb are presented. From the dependence of lamellar thickness on the crystallization undercooling at 5 kb, it is found that σe increases markedly with pressure leading to the formation of very thick crystals at high pressures. The magnitude of the increase in σe is in agreement with σe values calculated from the dependence of melting temperatures on pressure. The nucleus surface energy σe′ is not expected to vary significantly with pressure, and estimates of growth rates of 5 kb which indicate that the growth rate does not vary significantly with pressure at constant under-cooling confirm this. Fractionation effects and the differences in behavior between different polyethylenes are also discussed.
    Additional Material: 11 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 863-875 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Folded-chain crystals of certain polyamides present some novel diffraction effects due to the small number of repeat units within the lamellar thickness. X-ray diffraction evidence is available in the complete range from low to wide angles. This information is interpreted in terms of the structure factor of an individual lamella together with the lattice factor appropriate for the stacking of lamellae. When due account is taken of the lattice factor, whose effect can be detected even at large angles, three features of the lamellar structure can be deduced. First, the evidence is in favor of the straight-chain stems traversing almost the total thickness of each lamella, implying sharp folds at the lamellar surfaces. Some consequences of this result on the interpretation of data obtained from annealed mats are mentioned. Second, the detailed determination of the stem structure demands that the majority of the folds in nylon 66 lie in the acid group. Third, there are regions of depleted electron density at the lamellar surfaces, though features of the crystal structure are still retained. This indicates the presence of some folds deeper in the crystal than the majority.
    Additional Material: 7 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 11 (1972), S. 2099-2108 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A normal coordinate analysis for cyclic tetra-L-alanine molecule is reported. A comparison of amide modes and other low-frequency vibrations sensitive to conformational changes is made with those in poly-L-alanine. Intramolecular coupling coefficients are calculated using perturbation treatment.
    Additional Material: 3 Ill.
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  • 14
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase structure of a styrene-butadiene-styrene block copolymer (mol. wt. 21 000-98 0000- 21 000) film cast from tetrahydrofuran/methyl ethyl ketone is studied by light scattering. The scattered intensity I corresponding to Vv, Hv, Vh, and Hh polarization directions is measured as a function of scattering angle. From the In I vs sin2 (θ/2) plots the domain sizes are found to be about 0.4 and 1.0 μ. The a values are independent of polarization directions. This proves that the domains are geometrically isotropic. The two sizes correspond to two correlation distances; the smaller value represents the extent of heterogeneity within a spherical domain and the larger valued the inter-domain separation distance.
    Additional Material: 1 Ill.
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  • 15
    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: Sodium cellulosates were prepared by reacting premercerized cotton fabrics with sodium salts of selected alcohols. The degree of conversion to the cellulosate was related to the Taft polar substituent constant, σ*, of the alkoxide R group. Increase in size of the R group in the alkanol series did not decrease the degree of cellulosate formation. The extent of reaction of the cellulosates with 2-chloroethylidiethylamine in tertiary butanol to form diethylaminoethyl cellulose (DEAE-cotton) did not increase with the sodium ion content of the starting cellulosate substrate.
    Additional Material: 2 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 2449-2459 
    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 light-induced degradation of aqueous hydroxypropylmethylcellulose (HPMC; D.S. 1.9) solutions has been investigated under a variety of conditions. The HPMC was sensitized to short-wavelength radiation (〈500 nm) by the addition of sodium nitrite, the degradation being accompanied by increased acidity and the generation of oxides of nitrogen. Addition of eosin dye increased the sensitivity to visible light (〉500 nm), and the effect was considerably more pronounced when strong electron donors were added. Analysis of the shear-viscosity relationship of the solutions, during the degradation, indicated that both chain disentanglement and chain scission occurred but that the primary process was the depolymerization of the cellulose chain. It is proposed that both the dye- and nitrite-induced depolymerizations are a consequence of peroxide attack on the β-glucosidic ether link. The results indicate that, in the case of sodium nitrite addition, the peroxide was generated by the aqueous photolytic decomposition of the nitrite ion. The peroxide formation in the eosin - TEA system was a consequence of leuco-dye production, under the influence of the light, followed by the reduction of traces of dissolved oxygen by this activated dye.
    Additional Material: 4 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 615-626 
    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 effects of the chemical nature, concentration, stability, and location of various additives on the ultraviolet stability of polypropylene are discussed. It is shown that effective stabilizers of thin films do not depend on UV absorption for their protective action, whereas some relatively inefficient additives operate solely as UV screeners. Adequate UV protection was observed when small amounts (∼0.01 wt-%) of effective stabilizers were concentrated in or on the surfaces of commercial films, and the remaining bulk of the film contained only a very low concentration (∼0.01 wt-%) of uniformly blended additive. Previous attempts at demonstrating energy-transfer stabilization of the polymer are discussed with reference to the present data; it is concluded that effective polypropylene stabilizers probably operate by a combination of chromophore quenching, radical scavenging, and hydroperoxide decomposition.
    Additional Material: 2 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 99-106 
    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: Monofilament fibers were spun continuously from the free surface of a pool of molten poly(ethylene terephthalate) without the aid of a spinneret. For take-up velocities in the range of 12 to 400 ft/min, the denier of the filaments produced was an inverse power function of take-up velocity, and the birefringence was an inverse power function of the filament diameter. Production rate and product uniformity were strongly dependent on take-up velocity and surface temperature of the melt pool.
    Additional Material: 8 Ill.
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  • 19
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Ceramic and ceramic composite materials and devices were developed for specific maxillofacial applications. These applications included: (1) Replacement of hard tissue voids in low stress areas with a phosphate-bonded alumina-foamed ceramic and a calcium aluminate-bonded alumina foam; (2) development of porous ceramic-coated metallic devices for stabilization of mandibles with avulsed segments; (3) development of implantable ceramic tooth roots onto which more or less conventional crowns may be mounted.Efforts to date have been rewarding. Using the rhesus monkey for all experimental implant work, incorporation of porous ceramic foam prostheses to eliminate maxillary defects has been accomplished. Also, we have succeeded in stabilizing the mandible where segments of from 3 to 8 mm were removed. Bridging of the gap with new bone occurred within 6 weeks resulting in a total regeneration of the resected area with restoration of normal mandibular function. Finally, implantable tooth roots were developed. Three different surface treatment techniques have been used on a basic high-density alumina core. The first is a high-density matt finish which can only permit a fibrous tissue attachment or bony approximation but no ingrowth. The second is a porous alumina coating intended to permit bone ingrowth. The third is a rough surface consisting of particles of alumina sintered to the surface to maximize the bone/ceramic interface shear strength potential. Implantations of both anterior and posterior tooth roots with all three surface configurations have been successful for periods of up to six months.
    Additional Material: 11 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 79 (1972), S. 293-298 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The relative proliferative capacity of haematopoietic cell populations derived from 22-week-old adult bone marrow and 14-18 day foetal liver has been studied in lethally irradiated syngeneic recipients by means of chromosome markers. Although starting at a disadvantage in terms of the number of colony-forming units (stem cells) injected, the foetal liver-derived populations steadily increased their relative numbers in the myeloid and lymphoid tissues over a period of several weeks until a plateau was reached. It is suggested that stem cells in foetal liver have, on average, a higher intrinsic capacity for self-renewal than do those in bone marrow, and that this capacity falls to the adult level within about ten weeks of transfer.
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