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  • 1990-1994  (4)
  • 1
    ISSN: 1435-8107
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Cotton seed (Gossypium hirsutum L. cv. “Stoneville 825”), treated with 0, 0.2, 1.0, and 2.0 g active ingredient (a.i.) mepiquat chloride (MC) kg−1, was evaluated for the effect of MC on early plant growth. Emergence rate and total emergence of MC-treated seed and control were similar regardless of germination temperature. However, the number of leaves and squares and the dry weight of leaves, stems, and roots for hydroponically grown cotton plants were significantly lower at lower germination temperatures (15°C for 3 day/30°C for 1 day and 15°C for 4 days) than at higher germination temperatures (30°C for 4 days and 30°C for 3 days/15°C for 1 day). All MC treatments significantly decreased the number of nodes, leaves, and squares, as well as dry weight of leaves, stems, and roots, as compared to control plants at 28 days after emergence. MC seed treatments also significantly reduced plant height and total leaf area compared to controls. Water-use efficiency (WUE) was significantly lower for the 1.0 g a.i. MC treatment than for control plants. In general, the highest rate of MC seed treatment resulted in greater concentrations of calcium, phosphorus, and nitrogen in plant leaves and stems and also in greater concentrations of magnesium, phosphorus, and nitrogen in roots than in controls.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 45 (1994), S. 215-221 
    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: Metal dusting bei niedriglegierten StählenDas metal dusting zweier niedriglegierter Stähle wurde bei 475°C in strömenden CO-H2-H2O-Gemischen bei atmosphärischem Druck und aC 〉 1 untersucht. Die Reaktionsfolge läuft ab wie folgt: 1. Übersättigung mit C, Bildung von Cementit und dessen Zerfall zu Metallpartikeln und Kohlenstoff und 2. zusätzliche Kohlenstoffabscheidung aus der Atmosphäre auf den Metallteilchen. Die Geschwindigkeit der Metallabtragung r1 wurde durch Analyse des Korrosionsproduktes nach den Auslagerungen bestimmt, diese Geschwindigkeit ist zeitunabhängig und praktisch unabhängig von der Umgebung. Die Kohlenstoffabscheidung aus der Atmosphäre wurde mittels Thermogravimetrie bestimmt, die Geschwindigkeit der Abscheidung nimmt linear mit der Zeit zu, dies kann erklärt werden durch die katalytische Wirkung der Metallpartikel, weiterhin sind periodische Änderungen überlagert. Die Geschwindigkeit der Kohlenstoffabscheidung r2 ist proportional zu der Kohlenstoffaktivität in der Atmosphere. Das metal dusting konnte nicht durch eine Erhöhung der Sauerstoffaktivität unterdrückt werden oder durch Voroxidation, selbst unter Bedingungen, bei denen Magnetit stabil sein sollte. Zusätze von H2S jedoch unterdrücken wirksam den Angriff.
    Notes: The metal dusting of two low alloy steels was investigated at 475°C in flowing CO-H2-H2O mixtures at atmospheric pressure and aC 〉 1. The reaction sequence comprises: (1) oversaturation with C, formation of cementite und its decomposition to metal particles and carbon, and (2) additional carbon deposition on the metal particles from the atmosphere. The metal wastage rate r1 was determined by analysis of the corrosion product after exposures, this rate is constant with time und virtually independent of the environment. The carbon deposition from the atmosphere was determined by thermogravimetry, its rate r2 increases linearly with time, which can be explained by the catalytic action of the metal particles - periodic changes are superposed. The rate of carbon deposition r2 is proportional to the carbon activity in the atmosphere. The metal dusting could not be suppressed by increasing the oxygen activity or preoxidation, even if magnetite should be stable. Addition of H2S, however, effectively suppresses the attack.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 44 (1993), S. 89-97 
    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: „Metal dusting“ von HochtemperaturlegierungenMetal dusting, d. h. ein Zerfall in feine Metallpartikel und Kohlenstoff, wurde auf einer Auswahl von chromoxidbildenden Hochtemperaturlegierungen in einer strömenden CO-H2-H2O-Atmosphäre ausgelöst, bei Auslagerungen bei 650°, 600°, 500° und 450°C. Die Werkstoffe waren vorbehandelt worden durch Glühen in Wasserstoff bei 1000°C und Elektropolieren, dies führt zu grobkörnigem Gefüge und geringer Oberflächenverformung, beides ist nachteilig für die Ausbildung einer Cr2O3-Schicht. Der Widerstand gegen metal dusting hängt nur ab von der Fähigkeit, eine schützende Cr2O3-Schicht zu bilden, daher zeigen sich die hoch chromhaltigen ferritischen Stähle als sehr widerstandsfähig, die ferritischen Stähle mit 12-13% Cr waren weniger beständig. Aufgrund des niedrigeren Chromdiffusionskoeffizienten in den austenitischen Stählen waren diese sehr anfällig, insbesondere zwei Legierungen mit etwa 30% Ni (Alloy 800, AC 66). Für Nickelbasiswerkstoffe war das Erscheinungsbild des metal dusting etwas andersartig, aber auch diese wurden unter Grübchenbildung angegriffen. In allen Fällen geht dem metal dusting eine innere Karbidbildung voran, durch die das Chrom gebunden wird, nachdem kann die verbleibende Fe- oder Fe-Ni-Matrix zu dem instabilen intermediären Karbid M3C reagieren, das dann zerfällt zu Metallpartikeln und Kohlenstoff, im Falle der Nickelbasiswerkstoffe ist eine übersättigte feste Lösung von Kohlenstoff in dem Material das Zwischenprodukt.
    Notes: Metal dusting, i.e. disintegration into fine metal particles and carbon, was induced on a selection of chromia forming high temperature alloys in a flowing CO-H2-H2O atmosphere in exposures at 650°C, 600°C, 500°, and 450°C. The materials were pretreated by annealing in H2 at 1000°C and electropolishing, this leads to large grain size and low surface deformation, both is disadvantageous for formation of a Cr2O3 scale. The resistance to metal dusting is only dependent on the ability to form a protective Cr2O3 scale, thus the high Cr ferritic steels proved to be very resistant, the ferritic steels with 12-13% Cr were less resistant. Due to the lower Cr diffusivity in the austenitic steels, these were very susceptible, especially two alloys with about 30% Ni (Alloy 800, AC 66). The appearance of metal dusting was somewhat different for Ni-base materials but they were also attacked under pitting. The metal dusting is preceded in all cases by internal carburization whereby the chromium is tied up, afterwards the remaining Fe or Fe-Ni matrix can react to the instable intermediate carbide M3C which decomposes to metal particles and carbon, in case of Ni-base materials a supersaturated solid solution of carbon is the intermediate.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 21 (1994), S. 665-672 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Layers of the oxides FeO, Fe3O4, Fe2O3, Cr2O3 and Al2O3 were prepared by evaporation of the corresponding metal layers onto a preoxidized Si substrate and oxidation at elevated temperature. The oxidation was conducted under thermodynamically well-defined conditions so that the pure oxide phases noted were obtained. The oxide layer thickness was calculated from the thickness of the initial metal film, which was determined by chemical analysis and from the frequency change of a quartz crystal upon evaporaton. Auger electron spectroscopy depth profiles of the oxide layers were measured during Ar+ sputtering, and the sputter time necessary to reach the interface oxide/substrate was determined. The determination of this sputter time was not very exact, because the transition from oxide to substrate in the profile was rather gradual, owing to the roughness and crystalline character of the oxide layers that causes inhomogeneous sputtering. However, from the sputter time, oxide thickness and ion beam current, the sputter rates were obtained for the oxides noted (in nm μA-1 cm-2 min-1) and were compared to the sputter rate of amorphous Ta2O5, which is generally used as the sputter reference standard. Considerable differences were found. The results will lead to more reliable determinations of oxide scale thicknesses by sputtering.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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