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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 164 (1949), S. 787-788 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IN the course of a calorimetric investigation of the thermodynamic properties at low temperatures of the tetra-alkyl compounds of Group 4 elements, we have found that tin tetra-ethyl has an unusually large number of melting points. All these lie in the range 137–147° K. When this substance is ...
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 21 (1986), S. 2159-2168 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Bentonite-based cementitious materials have been formulated and evaluated in terms of their properties for use as cementitious lost-circulation control materials in geothermal wells at temperatures up to 300° C. The formulation which appears to have the highest potential as a new cementitious lost-circulation control material is composed of bentonite, ammonium polyphosphate, borax, magnesium oxide, and water. The appropriate combination of these ingredients results in the formation of slurries with viscosities and thickening times adequate to allow placement. After curing at elevated hydrothermal temperatures, the cement produced was characterized by a compressive strength 〉500 psi (〉3.45 MPa) at 2 h age, a permeability to water 〈2.0×10−4 Darcy, and a linear expansion 〉15%. The reaction compound responsible for the strength development at 300° C was found to be an assemblage of interlocking crystals composed of a grown thin-plate crystal. It was inferred that this microcrystalline cluster is associated with montmorillonite and ammonium polyphosphate-based complex formations.
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  • 3
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The ability of polyelectrolyte macromolecules to suppress the crystal growth of zinc phosphate (Zn · Ph) conversion coatings depends primarily on the functional pendant groups. The extent of segmental chemisorption of macromolecules having carboxylic and sulphonic acid groups on the embryonic crystal faces was found to be considerably higher than that of macromolecules containing amine groups. The reaction products formed by intermolecular reactions between amide groups in polyurethane coatings and carboxylic acid groups on the outermost surface of polyelectrolyte-modified Zn · Ph in Zn · Ph-to-polymer adhesive joint systems played an essential role in developing interfacial adhesive forces. A highly dense precipitation of Zn · Ph derived from a zinc orthophosphate dihydrate-based phosphating solution contributed significantly to reducing the corrosion rate of cold-rolled steel. It also was determined that the presence of an internally diffused polyelectrolyte in the Zn · Ph layers further enhances the resistance to corrosion of Zn · Ph itself.
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  • 4
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract It has been found that the outermost surface sites of polyacrylic acid-complexed crystalline zinc phosphate layers precipitated on cold-rolled steel surfaces act significantly to promote interfacial adhesive bonding to polymeric topcoats. This is the result of electrostatic internal diffusion and segmental chemisorption mechanisms of polyelectrolyte macromolecules either on newly precipitated crystal nuclei or on crystal growth sites during the primary zinc phosphate conversion process. The nature of the polymer-to-polymer chemical bond produced at the polymer-to-complex zinc phosphate precoat interfacial joints plays the key role in the achievement of long-term bond durability upon exposure to chemically corrosive environments. The locus of adhesive loss at the polymer-to-complex zinc phosphate joints after exposure to a hot acid solution was clearly identified to be cohesive failure in the crystalline precoat layers. A stable bond resulted from the formation of an interfacially produced hydrophobic structure by interactions between the polymer and the functional organic species existing on the complex precoat surfaces. The chemisorbed polyelectrolytes also served chemically to couple the organic coating and the inorganic zinc phosphate conversion layer.
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  • 5
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract An anhydrous α-Zn3(PO4)2 phase converted by the dehydration of hydrous zinc phosphate, Zn3(PO4)2·2H2O, crystal coatings in air at a temperature of approximately 300 °C, significantly enhances the corrosion resistance of steel, and also reduces the susceptibility of the crystals to alkaline dissolution. A subsequent α→γ phase transition at approximately 500 °C results in a poor protection behaviour, because of the formation of numerous microcracks on the crystal faces.
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  • 6
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
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  • 7
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A slow muon beam was passed through a thin aluminium foil and the emerging beam was studied for the presence of muonium in the 2S state. The fraction and the velocity distribution of the 2S muonium was determined.
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  • 8
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Muonic hydrogen isotopes (μ− p, μ− d, and μ−t) are simple quantum mechanical systems ideally suited for studies of numerous fundamental phenomena in electroweak and strong interactions as well as in applied areas such as muon chemistry or muon catalyzed fusion. Emission of muonic hydrogen isotopes into vacuum helps to overcome the limitations which are normally imposed on conventional investigations with gaseous and liquid targets. A proof of principle experiment for this new technique was performed at TRIUMF last year. Negative muons with 30 MeV/c momentum were stopped in a thin film of solid hydrogen and produced very low energy μ−d in vacuum. The distribution center of the normal velocity components of emitted μ−d atoms was measured to be ∼1 cm/μs. The yield of μ−d in vacuum is an increasing function of H2 film thickness δ up to a value of δ≥1 mm.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 2137-2155 
    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 nature of the interfacial interactions between functional levulinic-acid-modified furan resin coatings and crystalline zinc phosphate hydrate films deposited on carbon steel surfaces has been systematically investigated. The typical surface topography of the highly crystallized zinc phosphate films was found to be characterized by the presence of a dendritic microstructure array of interlocking triclinic crystals. This structure acts significantly to develop mechanical interlocking bonds with the functional blend polymer which penetrates into the open surface structure of the films. Both the thickness of deposition film and the polar H2O molecules of hydrate at the outermost film surface sites play essential roles in wetting by the functional liquid resin. When the polarized furan polymers spread on the oxide film surfaces, the carboxylate groups derived from the levulinic ester and acid molecules react to form strong hydrogen bonds with the crystallized H2O molecules on the hopeite film. This formation of hydrogen bonding was shown to be a major factor affecting the chemical intermolecular attractions. A formulation consisting of 95 parts furan to 5 parts levulinic acid was found to yield the optimum protective coating. More than 5 parts levulinic acid resulted in the transformation of the characteristics of the polymer film from hydrophobic to hydrophilic.
    Additional Material: 11 Ill.
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  • 10
    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 CaO-SiO2-H2O macromolecular-ionomer complex was found to be formed in the superficial layers of MMA-TMPTMA copolymer composite films made with filler containing hydraulic cement during exposure in an autoclave at temperatures up to 200°C. This complex acted to prevent the hydrothermal deterioration of the original composite films, which is important if the films are used as protective layers on metals. This complex also contributed significantly to hydrophobicity, a low energy surface, and less surface roughness, thereby lowering the intrinsic water permeability of the films. The glass transition temperature Tg and the tensile strength of the complexed films increased with increasing concentration of the cement additive used as a source of Ca2+ metallic ions, but they decreased when the cement concentration became excessive because of the chain enlargement caused by the growth of a large quantity of hydrated macromolecules. Ca2- ions were found to migrate from the cement grains in an aqueous medium and to have a crosslinking function connecting the oxidized metal surfaces and the functional carboxylate groups located in the pendent parts of the polymer molecules. The resultant shear bond strength of metal-to-metal lap joint specimens after exposure for 3 days to water at 150°C was twice as high as that for the samples made without cement.
    Additional Material: 21 Ill.
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