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  • Chemistry  (6)
  • Wiley-Blackwell  (6)
  • American Association for the Advancement of Science
  • American Chemical Society
  • American Journal of Science
  • American Society of Hematology
  • Elsevier
  • Springer
  • 1985-1989  (2)
  • 1980-1984  (2)
  • 1975-1979  (2)
  • 1965-1969
  • 1820-1829
  • 1998
  • 1988  (2)
  • 1984  (2)
  • 1979  (2)
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  • Wiley-Blackwell  (6)
  • American Association for the Advancement of Science
  • American Chemical Society
  • American Journal of Science
  • American Society of Hematology
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  • 1985-1989  (2)
  • 1980-1984  (2)
  • 1975-1979  (2)
  • 1965-1969
  • 1820-1829
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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
    Notes: The polymerization and crystallization of polyoxymethylene obtained by sublimation of trioxane (1,3,5-trioxane) and tetroxane (1,3,5,7-tetroxocane) crystals was investigated. Electron microscopy techniques and thermal analysis were used to characterize the polymer crystals as produced and after annealing. The polyoxymethylene crystals resulting from tetroxane show a regular lamellar folded chain macroconformation similar to those previously reported by polymerization of tetroxane crystals chemically initiated. The polymerization follows a crystallization succeeding polymerization mechanism. Trioxane gives mainly fibrous crystals, showing well oriented electron diffraction diagrams and higher melting points, consisting mostly of extended chains. A “pseudolamellar” morphology was also observed, being established by annealing, that the chain directions are parallel to the edges of the crystals. The strange growing habit seems to be produced by disruption of the electrical field of the trioxane crystals by a water effect. The polymerization seems to follow mainly a simultaneous polymerization and crystallization mechanism. The initiation of the polymerization is in both cases due to the gaseous formaldehyde formed during sublimation.
    Additional Material: 1 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 21 (1979), S. 333-336 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1871-1880 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic viscoelastic measurements on poly(vinyl chloride)/dioctyl phthalate gels have been carried out in parallel-plate shear mode. Two transitions are observed: the well-known gel-sol transition at temperature Tf, which probably corresponds to the beginning of fusion of crystalities, and a transition, at a temperature below Tf, denoted as Ts and corresponding to phase separation. The sub(gel-sol) Ts temperature is manifested as the transition from the first plateau zone to a second plateau in log G' versus temperature plots. Other techniques like polarizing microscopy and DSC measurements are not adequate for the detection of Ts.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1187-1202 
    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 morphologies of the as-produced polyethylenes obtained by slurry polymerization process of ethylene in n-heptane, using heterogeneous conventional and supported Ziegler-Natta catalysts, were investigated. The ability of four different catalytic systems in controlling the size and shape of the nascent polymer particles were tested. The catalytic systems employed were: the original Ziegler type catalyst produced by reduction of TiCl4 with Et2AlCl, the Natta type catalyst TiCl3-AA, the reduced TiCl4 with the metal carbonyls [Mo(CO)6 and Mn2(CO)10], and the supported TiCl4 on three commercial silicas having different surface areas: Davison 951, 952, and also the Dart 1000. It was found that the carriers affect the catalytic activity of the final catalyst and also its kinetic behavior. The supported Ziegler-Natta catalysts control more easily the nascent polymer particles (size, shape, and porosity) than the conventional ones. In addition the morphology of the catalysts and the subsequent polymer particles are closely related to the parent morphology of the silicas used as carriers. Furthermore, the nascent morphology of the polyethylenes obtained with the conventional TiCl4-Et2AlCl catalytic system can be modified by using different |Al|/|Ti| ratios, resulting in more dense, spherical, and bigger polymer particles by increasing this ratio. On the other hand, detailed studies on the texture or arrangement of the polymer particles reveal the existence of mainly two fine morphologies (globular and wormlike), which are the result of the order of the primary or elementary catalyst particles (microspheres and platelets), the force linking them together, and the activity of the polymerization centers placed on their surface.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 18 (1984), S. 643-654 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: On clot-promoting surfaces, intact normal blood or plasma deposits fibrinogen and then supplants it with high molecular weight kininogen (HMWK). On glass, plasma layers of less than about 25 μm thick, while still containing enough fibrinogen to coat the surrounding surfaces, lack sufficient HMWK per surface area to remove this fibrinogen deposit. Thus normal intact citrated plasma allowed to enter the space between a glass slide and a convex lens resting belly-down on the slide will leave a disc of fibrinogen where the thickness of plasma layer was below this “critical height” H. The discs of fibrinogen left by plasma that lacks HMWK pathologically or by activation or dilution, are larger - the required H being greater. The present study shows that plasma dilution (final volume divided by original plasma volume) plotted against H yields a straight line. In preliminary series, the slope of this line increases with the atomic weight of five metals whose oxidized surfaces were used as substrates. In whole blood collected in either heparin or ACD, a circle of platelets adheres to oxidized silicon, anodized tantalum, or glass; this circle is similar in size to the one of fibrinogen left by plasma.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 12 (1988), S. 247-252 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Oxidation/reduction processes occurring in rhodium particles supported on TiO2 have been studied by a combination of XPS and TPR/TPO. Rh(I) and Rh(III) are formed by calcination in excess of O2 at 773k, Rh(III) being favoured for samples with very small metal particles. For samples with particles in the range 2.0-10.0 nm, oxidation up to Rh2O of the whole particles occurs followed by a kinetically controlled growth of a thin Rh2O3 layer at their surface together with the formation of Rh(III) species at the particle/support interface. H2 adsorption at 300 K on the highly oxidized particles (up to Rh2O3) is an activated process which implies reduction of Rh(III) into Rh(I). Further reduction at 373 K leads to Rh(O) formation although some Rh(I) and Rh(III) species still remain unreduced up to T 〉 473 K. A model is proposed to decribe the evolution of these rhodium oxide particles as well as to explain their different behaviour against H2 adsorption at 300 K.
    Additional Material: 6 Ill.
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