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  • Polymer and Materials Science  (59)
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  • 11
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 173-178 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 14 (1993), S. 539-544 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 13
    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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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 977-988 
    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: In this paper, the synthesis of different catalytic systems based on the reduction of TiCl4 by Grignard compounds has been systematically studied. The catalysts exhibited the highest activities when used in the copolymerization of ethylene with n-hexene. The profile of the kinetic curves also changed when the comonomer was present during polymerization. By thermal analysis and scanning electron microscopy techniques, it could be found that the incorporation of the comonomer to the polymer chain brings about a decrease in the polymer crystallinities and an increase in the porosities of the growing particles. Due to that, the diffusion of the monomer to the catalytic active centers takes place more easily, consequently increasing the polymerization rate. In addition, catalysts control better the morphology (size and shape) of the nascent polymer particles when used for copolymerization.
    Additional Material: 7 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 911-917 
    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: Steady-state and transient shear flow properties of poly(vinyl chloride) and chlorinated polyethylene dissolved in dioctyl phthalate were studied at different temperatures and polymer concentrations. In the case of poly(vinyl chloride)/dioctyl phthalate systems the presence of a sol-gel transition temperature was observed, whereas for chlorinated polyethylene/dioctyl phthalate systems the mechanism of flow was the same in the whole range of temperatures and concentrations. On the basis of the data obtained for both polymer/solution systems, we conclude that the presence of crystallites, rather than hydrogen bonds, determines the rheological behavior of poly(vinyl chloride)/dioctyl phthalate systems.
    Additional Material: 6 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 347-352 
    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: A viscometric method to evaluate the enzymatic resistance of cellulosic ethers is proposed. The method was applied to samples of hydroxyethylcellulose (HEC) with molar substitution between 1.8 and 2.5. The results are discussed in terms of the values of Degree of Substitution and the average unsubstituted primary hydroxyl groups, obtained by high-resolution 13C-NMR of the neat polymers.
    Additional Material: 5 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 2151-2165 
    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: An investigation has been carried out for determining the effect of coupling agents on the mechanical properties of polymer-impregnated mortars. Mortar specimens were impregnated with methyl methacrylate (MMA) monomer and α, α-azobis-isobutyronitrile initiator, and polymerized thermally in water. Three titanate coupling agents, KR-33CS, KR-55, and KR-138s, and one silane coupling agent, the A-174, were used for the investigation. Varying amounts of coupling agent were used in impregnating the mortars in situ or in pretreating the mortars with a solvent system. Bulk polymerization of MMA shows no appreciable influence of the coupling agents in the reaction kinetics; however, with the exception of KR-138S, all polymers obtained in the presence of coupling agents came out as insolble. Similar results were obtained for polymers extracted with acetone from mortars. The mechanical property results show an improvement of properties in mortars containing 5.0 vol% of KR-33CS and A-174 after impregnation in situ. A slightly better improvements of mechanical properties were obtained by pretreating the mortar specimens with acetone or toluene/xylene containing coupling agents. Microscopic observation of the fracture surface showed no noticeable difference in the surfaces prepared with and without coupling agents.
    Additional Material: 4 Ill.
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  • 18
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to clarify the reaction mechanism of the solid-state polymerisation of 1,3,5-trioxane and 1,3,5,7-tetroxane as induced by gamma-radiation, the nascent textures and morphology of poly(oxymethylene) crystals were studied with light and transmission electron microscopy, X-ray scattering and differential thermal analysis techniques. In both cases poly(oxymethylene) crystals with fibrous morphology and “twin-structure” are obtained. The polymerization of 1,3,5,7-tetroxane gives rise to the formation of crystals where the preferred orientation of the polymer chain is the monomer b-axis; however, the fibrils showed ripples perpendicular to the main chain direction at a 70-240Å long period that depends extremely on the polymerization temperature. In the polymerization of 1,3,5-trioxane, POM crystals with 60% of the polymer chains in the direction of the monomer c-axis are obtained. The remaining chains are found in the “twin sub-crystals”. Dark field electron micrographs showed the sub-crystals to be an integral part of the fibrils. The material in the twin direction decreases, when the polymerization temperature or the yields increases; it never amounts to less than 30%. These results and the misfit between the lattices of the monomers and the nascent polymer indicate that the reactions which take place occur according to a simultaneous polymerization and crystallization mechanism through the gasphase. The polymerization process occurs easier at higher temperatures near the monomers' melting point due to the increase of monomer vapor pressure and diffusion processes in the monomer crystals. Molecular models of the chain growth are developed on the basis of the morphological observations.
    Additional Material: 19 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 733-742 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure and morphology of crystalline nylon 3 [poly(β-alanine)] have been studied by electron microscopy and x-ray diffraction. Two clearly defined forms are detected. Form I appears as spherulites made up of ribbonlike lamellae upon crystallization at high temperature from a solution in phenol-butanediol-1,4. They have monoclinic unit cell with a = 9.60 Å, c = 8.96 Å, and β = 122.5°. The hydrogen-bonded planes run parallel to the long dimension of the crystals. Form II is observed when the samples are prepared from formic acid solution at room temperature. A second type of spherulite with a microfibrillar structure is formed in this case. The isolated crystalline structures obtained from Form II appear to grow along the intersheet direction rather than along the hydrogen bond direction, which constitutes anomalous behaviour. Our results for this second form are consistent with an orthorhombic lattice with a = 9.56 Å and c = 7.56 Å. No clear information is obtained on the b dimension of the unit cell (chain axis) in either case. We assume a value of 4.78 Å, which corresponds to fully extended chains. The two forms coexist in films prepared from a formic acid-water solution as well as in samples recovered immediately after polymerization.
    Additional Material: 7 Ill.
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  • 20
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to elucidate the reaction mechanism of the chemically induced solid-state polymerization of 1,3,5,7-tetroxocane, the nascent morphology of poly(oxymethylene), (POM) crystals was investigated. The results show that POM has a lamellar morphology consisting of folded polymer chains. This morphology is different from that of the fibrous morphology obtained by radiation induced solid-state polymerization of 1,3,5,7-tetroxocane. Based on this the reaction takes place according to a crystallization succeeding polymerization mechanism, where the monomer passes through the gasphase to reach the reaction center.
    Additional Material: 10 Ill.
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