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  • 1
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Elektrochemische Impedanzspektroskopie als Hilfsmittel für die kontinuierliche Untersuchung der Passivierung und örtlichen Korrosion von AluminiumlegierungenLoch- und Spaltkorrosion von Aluminiumlegierungen sowie Verbundwerkstoffen mit Aluminiumlegierungen kann aufgrund der charakteristischen Veränderungen der Impedanzspektren im Bereich niedriger Frequenzen nachgewiesen werden. Ein Modell der Lochkorrosion, das in diesem Zusammenhang entwickelt wurde, stimmt mit experimentellen Daten überein. Mit Hilfe eines Anpassungsverfahrens wurde eine große Zahl von Daten ausgewertet, die mit Metallproben im Lieferzustand und mit Metallproben nach Passivierung in Certrichloridlösungen erhalten worden waren. Dieses chemische Passivierverfahren liefert Oberflächen mit hoher Beständigkeit gegen örtliche Korrosion. Al 6061, Al/SiC und Al/Graphit zeigten nach Passivierung in Certrichlorid (Behandlungsdauer 1 Woche) nach mindestens einem Monat in 0,5 n NaCl keine Lochkorrosion. Die elektrochemische Impedanzspektroskopie ist demnach ein bequemes Hilfsmittel zur Überwachung von Passivierungs- und Korrosionsprozessen.
    Notes: Pitting and crevice corrosion of Al alloys and Al-based metal matrix composites can be detected by characteristic changes of the impedance spectra in the low frequency region. A pitting model has been developed which is in agreement with the experimental data. A fitting procedure has been used to analyze a large number of data which have been obtained for as-received samples and samples which had been passivated in CeCl3 solutions. This chemical passivation process produces surfaces which are very resistant to localized corrosion. Al 6061, Al/SiC and Al/graphite which had been passivated in CeCl3 for one week did not pit in 0.5 N NaCl for at least one month. Electrochemical impedance spectroscopy (EIS) is a convenient tool for monitoring of the passivation and the corrosion processes.
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1261-1273 
    ISSN: 0887-6266
    Keywords: rod-like polyimide ; poly(amic acid) precursor ; imidization ; residual stress ; intrinsic stress ; thermal stress ; refractive index ; birefringence ; molecular in-plane orientation ; molecular ordering ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A soluble poly(amic acid) precursor solution of fully rod-like poly(p-phenylene pyromellitimide) (PMDA-PDA) was spin cast on silicon substrates, followed by soft bake at 80-185°C and subsequent thermal imidization at various conditions over 185-400°C in nitrogen atmosphere to be converted to the polyimide in films. Residual stress generated at the interface was measured in situ during imidization. In addition, the imidized films were characterized in the aspect of polymer chain orientation and ordering by prism coupling and X-ray diffraction. The soft-baked precursor film revealed a residual stress of 16-28 MPa at room temperature, depending on the soft bake condition: higher temperature and longer time in the soft bake gave higher residual stress. The stress variation in the soft-baked precursor film was not significantly reflected in the final stress in the resultant polyimide film. However, the residual stress in the polyimide film varied sensitively with variations in imidization process parameters, such as imidization temperature, imidization steps, heating rate, and film thickness. The polyimide film exhibited a wide range of residual stress, -7 MPa to 8 MPa at room temperature, depending on the imidization condition. Both rapid imidization and low-temperature imidization generated high stress in the tension mode in the polyimide film, whereas slow imidization as well as high temperature imidization gave high stress in the compression mode. Thus, a moderate imidization condition, a single- or two-step imidization at 300°C for 2 h with a heating rate of 〈 10 K/min was proposed to give a relatively low stress in the polyimide film of 〈 10 μm thickness. However, once a precursor film was thermally imidized at a chosen process condition, the residual stress-temperature profile was insensitive to variations in the cooling process. All the films imidized were optically anisotropic, regardless of the imidization history, indicating that rod-like PMDA-PDA polyimide chains were preferentially aligned in the film plane. However, its degree of in-plane chain orientation varied on the imidization history. It is directly correlated to the residual stress in the film, which is an in-plane characteristic. For films with residual stress in the tension mode, higher stress films exhibited lower out-of-plane birefringence, that is, lower in-plane chain orienta-tion. In contrast, in the compression mode, higher stress films showed higher in-plane chain orientation. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1261-1273, 1998
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 21 (1983), S. 1-11 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5543-5556 
    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 dielectric and optical properties of nitrogen-incorporated polyethylene films fabricated by radio-frequency glow discharge in ethylene-nitrogen (C2H4 - N2) gas mixtures have been measured for various nitrogen concentrations. The results show that the plasma-polymerized films have distinct properties from the ones based on conventional chemical polymerization. The incorporation of nitrogen in polyethylene results in an increase in breakdown strength, dissipation factor, and dielectric constant at frequencies below the optical frequency range, and in a decrease in dark conductivity, and in photoconductivity and extinction coefficient in the optical frequency range. However, the incorporation of nitrogen does not cause significant change in refractive index. The effects of the incorporation of nitrogen in polyethylene are attributed to the shallow acceptor-like traps introduced by incorporated nitrogen.
    Additional Material: 15 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4179-4189 
    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 incorporation of small amounts of a chlorinated hydrocarbon wax into polypropylene (PP) when making mica-PP composites is shown to produce a layer of degraded chlorinated hydrocarbon at the interface between the polymer and the reinforcement. Mica is shown to accelerate the thermal degradation of the chlorinated hydrocarbon, and the chlorinated hydrocarbon, or its degradation products, are shown to react with hydrocarbon analogues of the polymer. As well as modify the chemical nature of the interface, the layer of degraded chlorinated hydrocarbon is shown to modify the morphology of the interface by inhibiting the ability of the mica to nucleate the crystallization of PP from the melt.
    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 21 (1977), S. 1289-1295 
    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 engineering properties of polyurethane-poly(methyl methacrylate) simultaneous interpenetrating networks (SIN's) were evaluated. The hardness behavior reflected the observed phase inversion in the electron-microscopic studies. The maximum ultimate tensile strength was observed at 85% polyurethane-15% poly(methyl methacrylate) IPN and was due to the filler-reinforcing effect of the rigid poly(methyl methacrylate) phase. The ultimate tensile strenght of the 75/25 polyurethane-poly(methyl methacrylate) IPN was higher than that of the corresponding pseudo-IPN's (only one network crosslinked) and the linear blend. The leathery and glassy compositions did not show any reinforcement in the ultimate tensile strength. This indicated that the reinforcement in the ultimate tensile strength was not directly related to interpenetration (by increased physical entanglement crosslinks), but indirectly related by reducing the rigid phase domain sizes and increasing the adhesion between the two phases, thus enhancing the filler-reinforcing effect similar to that observed in a carbon black-filled rubber. The tear strengths of the polyurethane-rich IPN's pseudo-IPN's, and linear blends were found to be higher than that of the pure polyurethane as a combined result of increased modulus and tensile strength. The weight retentions in the thermal decomposition of the IPN's, pseudo-IPN's, and linear blends were higher than the proportional average of the component networks. The results seemed to indicate that this enhancement was related to the presence of the unzipped methyl methacrylate monomer. It was suggested that the monomers acted as radical scavengers in the polyurethane degradation, thus delaying the further reaction of the polyurethane radicals into volatile amines, isocyanates, alcohols, olefins, and carbon dioxide.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 381-391 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A procedure for the preparation of new block copolymers composed of a hydrophobic block of polystyrene, a hydrophilic spacer-block of poly(ethylene oxide) and a bioactive block of heparin was investigated. Polystyrene with one amino group per chain was synthesized by free radical oligomerization of styrene in dimethylformamide, using 2-aminoethanethiol as a chain transfer agent. This amino group was used in the coupling reaction with amino-telechelic poly(ethylene oxide) to produce an AB type diblock copolymer with one amino group per polystyrene (PSt)-poly(ethylene oxide) (PEO) chain. The amino-semitelechelic oligo-styrene was converted into the isocyanate-semitelechelic oligo-styrene using toluene 2,4-diisocyanate and subsequent coupling with H2N-PEO-NH2 afforded AB type block copolymers with terminal amino groups. The coupling of PSt-PEO-NH2 with heparin was performed in a DMF-H2O mixture, first by activating the heparin carboxylic groups with EDC at pH 5.1-5.2 and subsequently reacting the activated carboxylic groups with the amino groups of the PSt-PEO-NH2 at pH 7.5. Depending on the molecular weights of the diblock copolymer used 25-29% w/w heparin was incorporated. These polymers will be further evaluated for their blood-compatibility.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 397-397 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1693-1720 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel procedure for the synthesis of block copolymers composed of a hydrophobic block of polystyrene, a hydrophilic block of poly(ethylene oxide) and a bioactive block of nitrous acid-degraded heparin was developed. Amino-semitelechelic polystyrene was prepared by anionic polymerization of styrene in cyclohexane, using sec-butyllithium as initiator and N-(benzylidene)trimethylsilylamide as terminator. After purification using preparative column chromatography, polystyrene with one amino group per chain and a narrow molecular weight distribution was obtained. The terminal amino group was used in the coupling reaction with amino-telechelic poly(ethylene oxide) using toluene 2,4-diisocyanate to produce amino-semitelechelic polystyrene-poly(ethylene oxide) diblock copolymer (PS-PEO-NH2). The block copolymer was purified by preparative column chromatographic separations and had a narrow molecular weight distribution. Approximately one amino group per chain was found. When methylene 4,4′-diphenyl diisocyanate or hexamethylene diisocyanate were used as coupling agents low yields of PS-PEO-NH2 were obtained. Polystyrene-poly(ethylene oxide)-heparin triblock copolymer was synthesized in a DMF-H20 (40:1, v/v) mixture by a coupling reaction of PS-PEO-NH2 with nitrous acid-degraded heparin, in which aldehyde groups react with the primary amino groups of PS-PEO-NH2 at pH 7 in the presence of NaBH3CN via reductive amination. Using this procedure, 18-32% w/w heparin was incorporated, corresponding to ±1 PS-PEO chain per heparin molecule. These procedures enable the synthesis of well defined heparin containing block copolymers, which will be further evaluated for thier blood compatibility.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3167-3180 
    ISSN: 0887-624X
    Keywords: polybenzimidazole ; polyimide ; blends ; miscibility ; infrared spectroscopy ; poly(amic acid) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The precursor of polybenzimidazole (PBI), poly(3,3′-diamino-4,4′-benzidine isophthalamide) (PDABI), was synthesized from poly(3,3′-dinitro-4,4′-benzidine isophthalamide) (PDNBI) by reduction. With increasing temperature, the NH2 moiety which was protected by SnCl5-1 could cyclize and form PBI. Blends with polyamic acid (LaRC-TPI) were prepared. Clear blend films were prepared at up to 400°C. The IR spectra displayed shifts in the NH stretching band, thereby providing evidence for specific interactions related to the miscibility of their cured blends. © 1993 John Wiley & Sons, Inc.
    Additional Material: 26 Ill.
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