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  • Polymer and Materials Science  (27)
  • Computational Chemistry and Molecular Modeling  (6)
  • 1995-1999  (33)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 46 (1995), S. 405-409 
    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: Corrosion inspection in aircraft constructionThe inspections required on an aircraft during its operational phase are determined largely by the materials and constructions used. Practical experience has shown that corrosion can generally not be prevented on metallic aircraft structures, even if the surface protection systems have been chosen with great care. Constructions and materials used on aircraft and the result types of corrosion are described and the inspection concept is explained on the basis of this. Finally, typical inspection tasks are presented and the measurement results obtained with different NDT methods are presented and discussed.
    Notes: Die erforderlichen Inspektionen an einem Flugzeug in der Nutzungsphase werden wesentlich durch die verwendeten Werkstoffe und Bauweisen bestimmt. Die praktischen Erfahrungen zeigen, daß an metallischen Leichtbaustrukturen Korrosion generell nicht zu verhindern ist, auch bei sorgfältigster Auswahl der Oberflächenschutzsysteme, Luftfahrtspezifische Bauweisen und Werkstoffe und daraus resultierende Korrosionsarten werden vorgestellt. Darauf aufbauend wird das Inspektionskonzept erläutert. Anschließend werden typische Inspektionsaufgaben gezeigt und die Meßergebnisse mit verschiedenen zerstörungsfreien Prüfverfahren dargestellt und diskutiert.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 48 (1997), S. 207-215 
    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: Investigation on stress corrosion cracking of austenitic steels in cold chloride solutionsAt ambient temperatures of about 25°C austenitic chromium nickel steels can suffer stress corrosion in media with a concentration of both hydrogen ions and chloride ions exceeding 1 mol/L or in strongly concentrated chloride solutions. With the aid of constant strain rate testing and with U-bend specimens the parameters of this types of corrosion were investigated. Contrary to the situation with the acid solutions, the reproducibility of test results with the concentrated chloride solution was found to be low. The formation of martensite by cold working was found to be essential. The corrosion susceptibility decreases with increasing nickel content.Stress corrosion takes place within small critical potential ranges without a limit to more positive potentials as this is the case of stress corrosion with hot media. These potential ranges are widened with increasing cold working especially in the case of strongly grinding or cyclic loading in the plastic range.Corrosion cracking was observed with solutions of MgCl2, LiCl, with a less amount with NaCl, but not with ZnCl2. The concentration of chloride ions have an effect for solutions with a given kind of salt, but not for different salt solutions.
    Notes: Bei austenitischen Chrom-Nickel-Stählen kann transkristalline Spannungsrißkorrosion bei 25°C auftreten, wenn sowohl die Wasserstoffionen- als auch die Chloridionen-Konzentration etwa 1 mol/L überschreiten oder wenn stark konzentrierte Chloridlösungen vorliegen. Die Parameter dieser Korrosion wurden mit CERT-Versuchen und mit Bügelproben untersucht. Im Gegensatz zu den sauren Lösungen ist die Reproduzierbarkeit bei den konzentrierten Lösungen gering, wobei im wesentlichen die Bildung von Verformungsmartensit die Korrosionsanfälligkeit bestimmt, die mit ansteigendem Nickelgehalt abnimmt.Die Spannungsrißkorrosion findet in begrenzten Potentialbereichen statt und ist im Gegensatz zu der Spannungsrißkorrosion in warmer Medien zu positiveren Potentialen hin begrenzt. Die Potentialbereiche können mit zunehmender Kaltverformung ausgeweitet werden, wobei eine grobe Schleifbehandlung und zyklische Belastungen im plastischen Bereich die Rißbildung begünstigen.Rißbildung wurde in Lösungen mit MgCl2, LiCl und im geringen Ausmaß auch mit NaCl, nicht aber mit ZnCl2 beobachtet, wobei die Konzentration der Chlorid-Ionen nur innerhalb einer Salzart, nicht aber bei den verschiedenen Lösungen einen erkennbaren Einfluß hat.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 46 (1995), S. 607-607 
    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
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 48 (1997), S. 243-251 
    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: Corrosion of parts used for microelectronics applicationsManifestations of corrosion on parts used in microelectronics occur for different reasons and are frequently described in literature. They are not only caused by operational circumstances but are also favoured by the production process. Investigations have been carried out to ascertain the cause of the failure of several circuit boards used in the operation electronics of the preparation unit for kitchen waste water. During microscopic and electronmicroscopic observations of failed circuit boards, different corrosion types have been found, mainly on the surface of a commonly used Sn-Pb-alloy. Hence, potentiostatic and free-corrosion experiments under laboratory conditions have been performed using the employed Sn-Pb-alloy. In order to simulate the increased concentration of harmful substances at the surface of the boards, the medium used contained a high percentage of the substances found in the surroundings of the unit. From the measured values of current density for different potentials and the observed corrosion on the sample's surface, conclusions as to the reported failure of the electrical operation system have been made. During the experiments under laboratory conditions, manifestations of corrosion similar to those found on the surface of the failed circuit boards have been observed. Based on these results, it seems likely that pitting and selective corrosion of the Sn-Pb-alloy led to the failure of the investigated circuit boards and, therefore, of the operation electronics.
    Notes: Korrosionserscheinungen an Bauteilen der Mikroelektronik treten aus unterschiedlichen Gründen auf und sind in der Literatur beschrieben. Sie werden nicht nur durch die Betriebsumstände hervorgerufen, sondern werden nicht selten auch durch die Fertigung begünstigt. Untersuchungen zum Ausfall mehrerer Platten, die in der Steuerungselektronik einer Fettaufbereitungsanlage für Großküchenabwässer zum Einsatz gekommen sind, wurden durchgeführt. Bei der licht- und elektronenmikroskopischen Betrachtung der ausgefallenen Platine wurden verschiedene Korrosionserscheinungen gefunden, die hauptsächlich an dem eingesetzten Lötwerkstoff auftraten. Aus diesem Grund sind an der als Lötstoff eingesetzten Zinn-Blei-Legierung unter Laborbedingungen potentiostatische Halteversuche und Versuche hei freier Korrosion mit Medien durchgeführt warden, welche die Schadstoffe der Umgebungsluft der Anlage in erhöhten Mengen beinhalten, um damit ein Aufkonzentrieren an den Oberflächen der Platine zu simulieren. Anhand der ermittelten Stromdichte-Werte für verschiedene Potentiale und der Korrosionserscheinungen an den Proben werden Rückschlüsse auf den vorliegenden Schadensfall gezogen. Bei den unter Laborbedingungen durchgeführten Versuchen werden ähnliche Korrosionserscheinungen beobachtet, wie sie an den Bauelementen der ausgefallenen Platinen gefunden wurden. Es wird aufgrund der vorliegenden Ergebnisse Vermutet daß Lochfraß und selektive Korrosion der Sn-Pb-Legierung ursächlich für den Ausfall der untersuchten Platinen der Steuerungselektronik ist.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 283-295 
    ISSN: 0887-6266
    Keywords: thermal field-flow fractionation ; dynamic light scattering ; thermal diffusion ; polystyrene ; binary solvent mixtures ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal diffusion coefficient (Dτ) was determined for three polystyrene standards of different molecular masses in binary mixtures of tetrahydrofuran/dioxane and tetrahydrofuran/cyclohexane of various compositions. The Dτ values were obtained by combining retention data from thermal field-flow fractionation measurements with diffusion data from dynamic light scattering experiments. In agreement with earlier work of Schimpf and Giddings, the thermal diffusion coefficient was found to be virtually independent of the molecular mass of the polymers. In the binary mixtures of tetrahydrofuran and dioxane, both good solvents for polystyrene, the Dτ value was approximately equal to the average of the Dτ values in the pure solvents, weighted according to the mole fractions of the solvents in the mixture. However, for polystyrene in binary mixtures of tetrahydrofuran and cyclohexane this linear behavior of the thermal diffusion phenomenon was not observed. The addition of cyclohexane to tetrahydrofuran has initially only a minor effect on the molecular and thermal diffusion coefficients of the polystyrene standards. Because cyclohexane is a theta solvent for polystyrene, the preferential solvation of polystyrene by tetrahydrofuran could be an explanation for these results. © 1996 John Wiley & Sons, Inc.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 297-308 
    ISSN: 0887-6266
    Keywords: thermal field-flow fractionation ; dynamic light scattering ; diffusion NMR ; thermal diffusion ; polybutadiene/polytetrahydrofuran ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal diffusion coefficient (Dτ) was determined for polybutadiene and polytetrahydrofuran (i.e., polyoxytetramethylene) standards of different molecular masses in various organic solvents. The combination of thermal field-flow fractionation retention data with diffusion data from dynamic light scattering or diffusion NMR experiments yielded the thermal diffusion coefficients. In agreement with earlier work on thermal diffusion of polymers in solution, the thermal diffusion coefficient was found to be independent of the molecular mass of the polymers. However, this work once more indicates that the Dτ value is strongly influenced by the chemical composition of both the polymer and the solvent. © 1996 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 56 (1995), S. 523-531 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dielectric constant of a material is a macroscopic property that measures the reduction of the electrostatic forces between charged plates separated by the material, compared to a vacuum as intermediate material. It is next encountered as a scaling parameter in Coulomb's law for interacting charges, not only in the force, but also in the energy. In deriving the theory for dielectrics, the macroscopic nature is essential: Only then is the basic assumption that the dielectric material is homogeneous and isotropic a valid one. The appearance of the dielectric constant as a simple scaling factor in Coulomb's law has tempted many computational chemists to forget about the macroscopic nature of the dielectric and to apply the screened Coulomb's law between charges, supposedly in a low-dielectric medium such as proteins, in microscopic force fields. Optimization of force fields even led to distance-dependent “dielectric constants.” Another use of the dielectric constant appears in the dielectric continuum reaction field approaches for the computations of solvation energies and solvent effects. The solute is embedded in a cavity surrounded by the dielectric. Specific interactions between solvent molecules and solute are thus neglected. The cavity size and dielectric constants of interior and exterior are optimized for the model. The aim of this article is to show, by means of calculations on interacting point charges embedded in cavities surrounded by dielectrics and microscopic models of “low-dielectric” materials by explicit polarizabilities, that as far as the dielectric “constant” is concerned anything can happen, depending on the nature of the charges, the distance to the cavity boundary, the spatial arrangement of charges, and polarizabilities. Thus, a warning is issued to injudicious use of dielectric models in microscopic calculations. © 1995 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 25 (1997), S. 620-625 
    ISSN: 0142-2421
    Keywords: atomic force microscopy/lateral force microscopy (AFM/LFM) ; atomic resolution ; highly oriented pyrolytic graphite (HOPG) ; computer simulation ; stick-slip processes ; atomic scale friction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Although the atoms in cleavage planes of graphite are arranged in a honeycomb structure, it is well known from experimental work that atomic force microscopy (AFM) yields a hexagonal structure, a phenomenon that has not been understood so far. Here, computer simulations of the atomic-scale imaging process on graphite by AFM are reported, showing that this behaviour can be explained within a simple model of elastic tip-sample interaction. Both the topographic (AFM) images and the friction force or lateral force microscopy (LFM) images were simulated as a function of the scanning direction relative to the graphite lattice and as a function of the cantilever force constant. The scan distortions and the skipped area due to the AFM/LFM imaging process were evaluated. Simulations were performed both in the presence and in the absence of atomic-scale stick-slip processes. It is shown that neither stick-slip processes nor an inequivalence of the A- and B-sites of graphite is necessary to generate a hexagonal AFM image when scanning an atomic honeycomb structure. Rather, the simulations demonstrate that due to the two-dimensional elastic lateral displacement of the cantilever, the potential maxima - which correspond to the positions of the honeycomb lattice - are avoided by the scanning path of the tip apex, resulting in a hexagonal structure of the AFM and LFM images.© 1997 John Wiley & Sons, Ltd.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 16 (1995), S. 1445-1446 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
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  • 10
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Crystal surfaces of the layered dichalcogenide semiconductor rehenium disulphide (ReS2) grown by the vapour-phase transport technique were investigated by combined atomic force microscopy (AFM), lateral (—friction) force microscopy (LFM) and force modulation (—local elasticity) microscopy as well as scanning electron microscopy (SEM). The as-grown crystals exhibit atomically flat surfaces, on which circular islands with a typical diameter of 0.3 μm and a height of 30-50 nm have grown. While AFM only yields the topographic information, the simultaneously recorded lateral force and force modulation images give a clear material contrast, showing that on the islands the lateral forces are higher and the local elasticity is lower than on the bare ReS2 surface. The dependence of both the topographic and the lateral force images on the scanning direction is investigated. The results indicate that during crystal growth a different material, presumably ReBr3, has segregated on the surface of the ReS2 crystals. It is demonstrated that AFM in combination with LFM and force modulation microscopy can provide information on the composition of heterogeneous samples as well as the local mechanical properties of the different components.
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