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  • oxidation  (22)
  • Springer  (22)
  • American Geophysical Union
  • 2000-2004  (12)
  • 1980-1984  (10)
  • 1965-1969
  • 1950-1954
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  • Springer  (22)
  • American Geophysical Union
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 14 (1980), S. 263-277 
    ISSN: 1573-4889
    Keywords: oxidation ; Ni-Cr alloys ; two-phase alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Oxidation of the relatively simple, two-phase alloy Ni-70 wt.%Cr in oxygen between 1073 and 1473°K results in the formation of a Cr2O3 scale containing less than O.5 wt.% Ni in solid solution. The oxidation kinetics are irreproducible for an initial period, which is brief at 1073 and 1273°K but much more pronounced at 1473°K, both in duration and degree. This behavior is associated with the failure of the protective Cr2O3 scale. However, after longer periods a compact layer of Cr2O3 becomes established under isothermal conditions and results in a change to more reproducible kinetics, especially at 1073 and 1273°K. Oxidation causes chromium depletion and the formation of a single-phase zone which separates the scale and the two-phase bulk alloy. The depth of Cr2O3 internal oxide coincides with this zone. The oxidation behavior is compared with that of more Ni-rich, single-phase Ni-Cr alloys, with particular reference to the effects of the constitution of the underlying alloy and the integrity of the protective oxide.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 18 (1982), S. 295-314 
    ISSN: 1573-4889
    Keywords: Nickel-manganese alloys ; oxidation ; solid solution scales ; internal oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Ni-Mn alloys containing up to 38% Mn have been oxidized in pure oxygen between 873 and 1273 K and the parabolic rate constants measured. The scale morphologies and oxide compositions are interpreted in terms of modifications to the scale on pure Mn caused by the presence of Ni. The scales are composed predominantly of two layers at all temperatures, giving the sequences of phases alloy/cubic monoxide (Ni, Mn)O/ternary spinel, with the cubic (Ni, Mn)O layer always having the greater thickness. There is limited evidence for a third, very thin, outer layer in the scales on all alloys at 873 K and for Ni-38%Mn at 1073 K, which is tentatively considered to be Mn2O3, giving layers in the order alloy/cubic monoxide/ternary spinel/Mn2O3, by analogy with the scale formed on pure Mn. The distribution of the alloy components in the scale is discussed in relation to the Ni-Mn-O phase diagram and in terms of recent theoretical treatments of solid solution scale formation on binary alloys, as far as the available diffusion data allow. The occurrence of internal and intergranular oxidation and the formation of a Mn-depleted zone coincident with the band of uniform internal oxide are considered briefly.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of peptide research and therapeutics 7 (2000), S. 347-351 
    ISSN: 1573-3904
    Keywords: chromogenic substrates ; oxidation ; Oxone® ; para-nitroanilides ; solid-phase synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new strategy has been developed for the rapid synthesis ofpeptide para-nitroanilides (pNA). The method involves derivatization of commercially available tritylchloride resin(TCP-resin) with 1,4-phenylenediamine, subsequent coupling withdesired amino acids by the standard Fmoc protocol, and oxidationof the intermediate para-aminoanilides (pAA) with Oxone®. This procedure allows easy assembly of the desired para-aminoanilides (pAA) on standard resin and efficient oxidation and purification of the corresponding para-nitroanilides (pNA). The method allows easy access to any desired peptide para-nitroanilides, which are useful substrates for the characterization and study of proteolytic enzymes.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    International journal of peptide research and therapeutics 7 (2000), S. 347-351 
    ISSN: 1573-3904
    Keywords: chromogenic substrates ; oxidation ; Oxone® ; para-nitroanilides ; solid-phase synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new strategy has been developed for the rapid synthesis of peptide para-nitroanilides (pNA). The method involves derivatization of commercially available tritylchloride resin (TCP-resin) with 1,4-phenylenediamine, subsequent coupling with desired amino acids by the standard Fmoc protocol, and oxidation of the intermediate para-aminoanilides (pAA) with Oxone®. This procedure allows easy assembly of the desired para-aminoanilides (pAA) on standard resin and efficient oxidation and purification of the corresponding para-nitroanilides (pNA). The method allows easy access to any desired peptide para-nitroanilides, which are useful substrates for the characterization and study of proteolytic enzymes.
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  • 5
    ISSN: 1572-879X
    Keywords: alkylbenzene ; toluene ; ethylbenzene ; xylene ; mesitylene ; p‐ethyltoluene ; cumene ; p‐cymene ; oxidation ; palladium ; 1,10‐phenanthroline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Only the side‐chain oxidation of alkylbenzenes (R–C6H3–R′–R″ R=H, Me, Et, Pri R′=H, Me; and R″=H, Me) by oxygen (35–50 atm, 200)C° is promoted in the presence of [Pd(phen)(OAc)2].
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 11-12 (2000), S. 359-367 
    ISSN: 1572-9028
    Keywords: zeozyme ; encapsulated complexes ; copper acetate ; copper dimers ; enzyme mimic ; EPR of copper ; tyrosinase ; oxidation ; oxygenase ; tyrosine oxidation ; phenol oxidation ; hydroxylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxygenase mimicking activity of copper acetate dimers in the regioselective ortho-hydroxylation of L-tyrosine to L-dopa is enhanced on encapsulation in zeolite Y. The structure and magnetic properties of the catalytic active site were characterized by EPR spectroscopy. The spectra of this “zeozyme” reveal the presence of (1) copper acetate dimers in the supercages and (2) isolated Cu(II) ions in the sodalite cages of the zeolite. There are significant differences in the EPR spectra of the “neat” and encapsulated complexes: on encapsulation in zeolite, the Cu–Cu exchange coupling constant, −, increases to 310 from 259 cm−1 for the “neat” complex (i.e., by about 19.7%). Simultaneously the Cu–Cu separation in the dimer, estimated indirectly from the exchange coupling constant, shortens to 2.40 Å in the encapsulated state from 2.64 Å in the “neat” complex. There is, hence, a relatively greater overlap of the metal orbitals of the dimer copper atoms inside the restricted confines of the zeolite cages. The consequent, enhanced, trans axial lability of the phenolate and dioxygen ligands promotes the catalytic oxygenase activity of copper acetate dimers on encapsulation in zeolites. A causal relationship between changes in the structural features of an active site on encapsulation in the zeolite and the corresponding catalytic activity has, thus, been established.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 64 (2000), S. 113-118 
    ISSN: 1572-879X
    Keywords: X‐ray photoelectron spectroscopy (XPS) ; scanning electron microscopy (SEM) ; silver ; oxidation ; surface chemical reaction ; NO ; NO x
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The behavior of a AgNO3/Ag2O/Ag “sandwich” upon heating in vacuum was studied by in situ X‐ray photoelectron spectroscopy (XPS) and ex situ scanning electron microscopy (SEM). The AgNO3/Ag2O/Ag “sandwich” was prepared by exposure of a silver foil to a NO : O2 mixture. The upper layer of the “sandwich” consists of AgNO3 crystals of a mean size between 0.1 and 0.4 μm. Heating at 550 K in vacuum results in melting of the AgNO3 crystals. A liquid film of AgNO3, readily wetting the silver, covers the surface. Cooling below the melting point of AgNO3 leads to the agglomeration of silver nitrate to long islands with a size reaching a few tens of micrometers (μm). The possible effects of AgNO3 liquid‐phase formation on surface processes are discussed.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 23 (1982), S. 147-150 
    ISSN: 1432-1041
    Keywords: methaqualone ; debrisoquine ; pharmacogenetics ; metabolism ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The metabolism of methaqualone to the glucuronides of 5 C-monohydroxy metabolites and to the N-oxide has been studied in 2 groups of healthy young adults phenotyped as extensive and poor metabolisers of debrisoquine. No significant interphenotype differences were observed with respect to the excretion of any of the 6 metabolites. It is probable that the genetic regulation of the pathways leading to these metabolites is at a locus other than that which is responsible for the regulation of the oxidation of debrisoquine, guanoxan, phenacetin, phenytoin and sparteine.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 63 (2000), S. 507-515 
    ISSN: 1572-8943
    Keywords: boron carbide ; kinetic modelling ; oxidation ; water vapour
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxidation behaviour of a B4C based material was investigated in a dry atmosphere O2(20 vol.%)-CO2(5 vol.%)-He and also in the presence of moisture H2O (2.3 vol%) as boron oxide is very sensitive to water vapour. The mass changes of samples consisting of a chemical vapour deposit of B4C on silicon nitride substrates were continuously monitored in the range 500–1000°C during isothermal experiments of 20 h. The stability of boron oxide formed by oxidation of B4C was also studied in dry and wet atmospheres to explain the kinetic curves. In both atmospheres, oxidation is diffusion controlled at 700 and 800°C and enhanced by water vapour. At 900°C and higher temperatures, boron oxide volatilisation and consumption by reaction with water vapour modifies the properties of the oxide film and the material is no more protected. At 600°C, B4C oxidation is weak but the process remains diffusion controlled in dry conditions as boron oxide volatilisation is negligible. However, in the presence of water vapour, B2O3 consumption rate is significant and mass losses corresponding to this consumption and to the combustion of the excess carbon are observed.
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  • 10
    ISSN: 1573-4889
    Keywords: ion plating ; steel ; TiAlN coating ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract To improve the high-temperature oxidation resistance of STD61 steels used ashot dies or cutting tools, Ti0.3Al0.2N0.5films were deposited on STD61 steel substrates by arc-ion plating. Thedeposited film consisted of Ti3Al2N2 andTi2N phases. The oxidation characteristics were studied attemperatures ranging from 700 to 900°C in air. The deposited STD61steels displayed excellent oxidation resistance up to 800°C, butexhibited large weight gains and breakaway oxidation at 900°C. Theoxidation products were primarily Fe2O3, TiO, TiO2,and α-Al2O3, the relative amount of each oxidebeing dependent on the oxidation condition. Among various oxides, TiO2and α-Al2O3 were the major oxides at 800°Cfor at least up to 16 hr. However, at a higher temperature or a longeroxidation period, the significant outward diffusion of iron from thesubstrate resulted in the formation of iron oxides, together with otheroxides of Ti and Al.
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