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  • oxidation
  • Springer  (73)
  • American Meteorological Society
  • 1995-1999  (47)
  • 1990-1994  (26)
  • 1955-1959
  • 1999  (47)
  • 1990  (26)
Collection
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  • 1995-1999  (47)
  • 1990-1994  (26)
  • 1955-1959
Year
  • 1
    ISSN: 1572-8773
    Keywords: acidophilic ; strain ; oxidation ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Recovery of metal values from sulfide ores by use of acidophilic microorganisms is gaining importance. A number of commercial/pilot plants are setup to find out the techno-economic feasibility of the overall process. The main drawback in the process is the slow kinetics of dissolution of metal values from the sulfide ores. To make the technology e attractive the kinetics should be improved considerably. There are various factors which determine the overall kinetics such as bacterial activity and concentration, iron and sulfur oxidation, oxygen consumption, reactor design and nature of ore. A brief review has been made dealing with the above parameters
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  • 2
    ISSN: 1572-879X
    Keywords: propane ; oxidation ; calcium-based catalysts ; tetrachloromethane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxidation of propane has been investigated in the presence and absence of tetrachloromethane (TCM) on calcium hydroxyapatite (CaHAp), Ca3(PO4)2, CaSO4 and CaO at 723 K. In the absence of TCM, the conversion of C3H8 on CaHAp was 7.7–9.2% during 6 h on-stream while that on Ca3(PO4)2, CaSO4 and CaO was 0.6, 0 and 0.2–0.4%, respectively. The principal products on all catalysts in the absence of TCM were CO and CO2 with small selectivities to C3H6 and C2H4 (both 5–6%) observed on CaHAp. Upon addition of TCM, the selectivity to C3H6 on all catalysts and the conversion of C3H8 on CaSO4 increased while, with increasing time-on-stream, the changes in the conversion and selectivity were dependent upon the nature of the catalysts. XPS and XRD analyses provide evidence for the presence of chlorine in the surface and/or bulk of three of the catalysts, suggesting that chlorinated species on the solids play a role in the selectivity enhancement, but the absence of chlorine from the sulphate demonstrates the dissimilarities of the catalysts in their abilities to sorb and decompose TCM.
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  • 3
    ISSN: 1572-879X
    Keywords: methane ; oxidation ; strontium hydroxyapatite ; lead hydroxyapatite ; tetrachloromethane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxidation of methane has been investigated on lead hydroxyapatite (PbHAp), strontium hydroxyapatite (SrHAp) and their binary mixtures at 873 K. PbHAp showed no activity for the oxidation of methane, while SrHAp produced carbon monoxide selectively at 2–4% conversion. On binary mixtures of the hydroxyapatites the conversion of methane and the selectivity to C2 compounds reached values higher than those of the separate constituents of the mixture. With tetrachloromethane in the feed stream a similar synergistic effect was observed with conversions of methane and selectivities to CH3Cl higher on the binary mixtures than those on either SrHAp or PbHAp. The strontium-containing hydroxyapatite appears to play a crucial role in the activation of methane, while the presence of the lead-containing analogue is apparently required for the minimization of undesirable processes involving methyl radicals.
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  • 4
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    Catalysis letters 7 (1990), S. 241-251 
    ISSN: 1572-879X
    Keywords: Fischer-Tropsch synthesis ; iron based catalysts ; Fe ; Co ; Ru catalysts ; fixed bed reactors ; fluidized bed reactors ; sulfur poisoning ; oxidation ; coke fouling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Because of the decreased profitability of making synthetic fuels, Sasol intends expanding its production of the higher valued chemicals, in particular waxes and olefins. The advantages and disadvantages of using Fe, Co and Ru catalysts are discussed from the point of view of costs, availability, product selectivity, activity and sensitivity to poisons. The loss of activity and selectivity of iron based catalysts in both fixed and fluidized bed reactors is discussed. The main contributing factors are sulfur poisoning, oxidation and coke fouling. In fixed bed reactors sulfur poisoning and “coke” laydown deactivates the front end of the bed while hydrothermal sintering/oxidation deactivates the back end. In fluidized beds the deposition of large amounts of Boudouard carbon doesnot markedly lower the activity. The smaller catalyst particles end up consisting of small iron carbide entities embedded in a matrix of carbon. The larger catalyst particles consist of cores of inert magnetite surrounded by the carbide/carbon matrix. FT reactor development at Sasol is briefly reviewed.
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  • 5
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    Catalysis surveys from Japan 3 (1999), S. 55-60 
    ISSN: 1572-8803
    Keywords: acetic acid ; oxidation ; Pd ; heteropoly acid ; ethylene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new process for acetic acid production by direct oxidation of ethylene which was established and commercialized is described. The catalyst system consisting of Pd and heteropoly acid exhibits excellent activity and selectivity. The addition of Se or Te to the catalyst system is effective to suppress the formation of carbon dioxide. This new process is applicable to a plant of a wide range of size corresponding to the local demand. Because this new process produces little waste water, it is very friendly to the environment.
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  • 6
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    Catalysis letters 57 (1999), S. 109-113 
    ISSN: 1572-879X
    Keywords: superacid ; zirconia ; molybdenum oxide ; methane ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A series of zirconia-supported molybdenum oxide catalysts with different molybdenum loadings prepared using conditions reported to generate “superacidity” have been evaluated for their performance as catalysts for methane oxidation. A marked dependence of Mo content on activity has been observed, with the most active material being that with intermediate molybdenum content. 5 wt% MoO3/ZrO2 compares favourably with ZrxCe1-xO2 for methane combustion. The presence of MoO3 is observed to stabilise the tetragonal polymorph of ZrO2 and, as Mo content is increased, dispersed MoO3 crystallites are formed as evidenced by Raman spectroscopy. Temperature-programmed reduction studies evidence differences in the reduction behaviour of the materials as a function of loading. The results indicate that molybdenum oxide supported on monoclinic zirconia gives rise to the most active catalyst. It is tentatively suggested that the formation of a MoO3 monolayer during reaction may be of importance.
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  • 7
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    Catalysis letters 6 (1990), S. 181-186 
    ISSN: 1572-879X
    Keywords: Metals for catalysis “syngas” ; oxidation ; nickel ; platinum group metals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Partial oxidation of methane to synthesis gas has been carried out over a number of transition metal catalysts under a range of conditions. It is found that the metals Ni, Ru, Rh, Pd, Ir and Pt, either supported on alumina or present in mixed metal oxide precursors, will bring the system to equilibrium. The yield of CO and H2 improves with increasing temperature in the range 650–1050 K, and decreases with increasing pressure between 1 and 20 atm. An excellent yield (∼92%) is obtained with a 4∶2∶1 N2∶CH4∶O2 ratio at 1050 K and atmospheric pressure, with a space velocity of 4×104 hour−1.
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  • 8
    ISSN: 1572-879X
    Keywords: Ultraviolet heterogeneous photocatalysis ; oxidation ; trichloroethylene ; titania ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Kinetics of the gas/solid heterogeneous photocatalytic oxidation of dilute trichloroethylene (TCE) vapors by ultraviolet-illuminated titanium dioxide have been determined using a fixed-bed dynamic photoreactor. Reaction rate dependences on inlet TCE, oxygen and water vapor concentrations were found to consist of both reactant sensitive and insensitive regions. In the reactant sensitive regions, measured limiting apparent reaction rate orders for TCE, oxygen and water vapor are 0.8, 1.7 and — 3, respectively. Water vapor in the reactant stream lowersinitial reaction rates relative to corresponding water free conditions, but is required to sustain photocatalytic activity for extended periods of time.
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  • 9
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    Catalysis surveys from Japan 3 (1999), S. 27-35 
    ISSN: 1572-8803
    Keywords: oxidation ; oxygen ; alkane ; N‐hydroxyphthalimide ; radical catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A practical catalytic method to convert alkanes into the corresponding oxygen‐containing compounds with O2 under mild conditions using N‐hydroxyphthalimide (NHPI) in the presence or absence of a transition metal was developed. Thus, cyclohexane was successfully converted into adipic acid in good conversion and selectivity by a combined catalytic system consisting of NHPI and Mn(acac)2. Lower alkane such as isobutane was converted into t‐butyl alcohol (83%) under 10 atm of air by NHPI‐Co(OAc)2 system. Alkylbenzene such as toluene was oxidized to benzoic acid in high yield (81%) under normal temperature and pressure of dioxygen in the presence of a catalytic amount of NHPI and Co(OAc)2. ESR measurements showed that phthalimide‐N‐oxyl generated from NHPI under dioxygen atmosphere is a key species in this oxidation and functions as a radical catalyst.
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  • 10
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    Journal of solid state electrochemistry 3 (1999), S. 179-186 
    ISSN: 1433-0768
    Keywords: Key words Cathodic protection system ; Carbon ; oxidation ; Composite carbon/polymer anode ; Lifetime
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The suitability of a polymeric composite material for use as part of an anode structure in a cathodic protection system has been examined. The composite material was a conductive blend (volume resistivity typically 1.5 Ω cm) of carbon black in a polyethylene binder. A long operational lifetime for the material demands that the rate of carbon loss must be low. In the work reported here, electrochemical and in situ analytical techniques were employed to characterise the performance of the material over a wide range of anodic current densities in a variety of aqueous electrolytes. The predominant anodic electrochemical reaction on the polymeric material is CO2 formation in acid and neutral solutions, which causes loss of carbon from the surface and the development of a non-conducting layer of polyethylene. The characteristics of the reaction suggest that it occurs via the discharge of H2O. In alkaline pH, however, the anodic reactions are more complex. A high OH− concentration (pH 12 or higher) favours the formation of oxygen rather than CO2, particularly at low anodic potentials. The presence of CO3 2− in the electrolyte catalyses the evolution of oxygen at pH values as low as 9. The electrochemical formation of oxygen always occurs in parallel with the generation of some humic acid in the solution.
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  • 11
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    Microchimica acta 102 (1990), S. 271-276 
    ISSN: 1436-5073
    Keywords: mercaptans ; oxidation ; disulphide ; Chlorobenzotriazole ; potentiometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A simple but accurate potentiometric method for the estimations of mercaptans in 0.01M perchloric acid has been developed, based on their oxidation with 1-Chlorobenzotriazole. Quantitative oxidation solely to the disulphide stage is ensured by using critical amounts of methanol, acetonitrile and potassium iodide. Chloride, mercury(II) and copper(II) interfere. A back-titration procedure can also be used. The oxidation products have been identified.
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  • 12
    ISSN: 1432-072X
    Keywords: Key words Heterologous expression ; Methane ; oxidation ; Methane monooxygenase ; Methanotroph ; Regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The methanotrophs Methylococcus capsulatus (Bath) and Methylosinus trichosporium OB3b contain particulate methane monooxygenase (pMMO) and soluble methane monooxygenase (sMMO) genes. Other methanotrophs such as Methylomicrobium album BG8 and Methylocystis parvus OBBP contain only pMMO genes. Although molecular genetic techniques are poorly developed in methanotrophs, sMMO genes were expressed in methanotrophs normally containing only pMMO genes. This was achieved by conjugation using broad-host-range plasmids containing the native promoter and sMMO genes from Mc. capsulatus (Bath) and Ms. trichosporium OB3b. sMMO genes derived from Ms. trichosporium OB3b were expressed in an active form in Mcy. parvus OBBP and in Mm. album BG8. Therefore, all of the genes required for active sMMO synthesis were contained on the broad-host-range plasmids and were expressed in the heterologous hosts. Constitutive synthesis of pMMO was observed in Mm. album BG8 when grown at high and low copper-to-biomass ratios, while transcription of the recombinant sMMO genes was only observed under growth conditions of low copper-to-biomass ratios. Therefore, the regulatory protein(s) for sMMO synthesis was also present on the plasmid used, or the heterologous host contained a regulatory system for sMMO. Expression of sMMO genes in methanotrophs containing only pMMO will assist further investigations on the expression and regulation of MMO genes in methanotrophs.
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  • 13
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    Journal of thermal analysis and calorimetry 57 (1999), S. 875-881 
    ISSN: 1572-8943
    Keywords: charge transfer ; Kelvin probe ; oxidation ; work function ; zirconia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The extent of the surface charge, that develops during oxidation of zirconia, is determined using work function measurements for both bulk specimen and thin films. The bulk specimen of yttria-doped zirconia (10 mol%) exhibits maxima of the surface electrical effect at 373 and 973 K (130 and 280 mV, respectively) that can be considered in terms of oxygen chemisorption and oxygen non-stoichiometry. Thin film of undoped zirconia exhibits a maximum at 473 K (260 eV). Addition of yttria (10 mol%) to the thin film results in a substantial reduction of the maximum, to about 140 eV, that is shifted up to 600 K.
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  • 14
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    Journal of thermal analysis and calorimetry 57 (1999), S. 473-486 
    ISSN: 1572-8943
    Keywords: cumene ; oxidation ; polymerization ; quinone-amine inhibitors ; solution microcalorimetry ; styrene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The application of solution microcalorimetry was demonstrated on two model examples – inhibited oxidation of cumene and radical polymerization of styrene. From the experimental dependences of the rate of heat release on time, the rate constants k 7 of the interaction of an inhibitor with radicals of substrate (RO 2 . or R.) in oxidation or in polymerization were determined for the set of inhibitors of N-aryl N-(2-quinone) amine series. It was shown that these compounds are weak inhibitors of oxidation of cumene and rather efficient inhibitor of polymerization of styrene.
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  • 15
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    Plasma chemistry and plasma processing 19 (1999), S. 131-151 
    ISSN: 1572-8986
    Keywords: Styrene ; oxidation ; silent discharge ; plasma ; dielectric barrier
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract A silent discharge plasma reactor has been developed to study the oxidation of styrene vapor in argon/oxygen mixtures. A number of analytical techniques were employed to determine the destruction efficiency and to characterize the intermediate products. The destruction efficiency was measured as a function of initial styrene concentration, temperature, and energy density of the plasma. The formation of solid products was observed in most experiments. At low temperature (100°C), the solid deposit was polymeric in nature, while at high temperature (300°C) the solid appeared to be amorphous carbon. A combination of high temperature and high energy density resulted in high destruction efficiency and minimal production of solid films. The destruction efficiency vs. energy density is shown to be more complex than a simple model predicting exponential behavior. Several reasons for the discrepancy are suggested. The “e-folding” energy density for the destruction of styrene is compared to literature values for other organic compounds, measured using similar types of plasma reactors.
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  • 16
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    Plasma chemistry and plasma processing 19 (1999), S. 383-394 
    ISSN: 1572-8986
    Keywords: Nonthermal plasma ; benzene ; Al2O3 ; BaTiO3 ; oxidation ; absorption ; atmospheric pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract The combination of plasma discharge and adsorption was examined for oxidation of dilute benzene in air in a plasma reactor packed with a mixture of BaTiO 3 pellets and porous Al 2 O 3 pellets (i.e., an alumina hybrid reactor). The oxidative decomposition of benzene was enhanced by the benzene concentrating on the Al 2 O 3 pellets. Furthermore, there was a higher selectivity to CO 2 in the products from the hybrid than from a plasma reactor packed with BaTiO 3 pellets alone. The presence of the Al 2 O 3 pellets suppressed the formation of N 2 O.
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  • 17
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    Plasma chemistry and plasma processing 19 (1999), S. 421-443 
    ISSN: 1572-8986
    Keywords: Streamer corona ; NO x removal ; nonthermal plasma ; oxidation ; reduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract In this paper, the NO-to-NO 2 conversion in various gaseous mixtures is experimentally investigated. Streamer coronas are produced with a dc-superimposed high-frequency ac power supply (10–60 kHz). According to NO x removal experiments in N 2 +NO x and N 2 +O 2 +NO x gaseous mixtures, it is supposed that the reverse reaction NO 2 +O→NO+O 2 may not only limit NO 2 production in N 2 +NO x mixtures, but also increase the energy cost for NO removal. Oxygen could significantly suppress reduction reactions and enhance oxidation processes. The reduction reactions, such as N+NO→N 2 +O, induce negligible NO removal provided the O 2 concentration is larger than 3.6%. With adding H 2 O into the reactor, the produced NO 2 per unit removed NO can be significantly reduced due to NO 2 oxidation. NH 3 injection could also significantly decrease the produced NO 2 via NH and NH 2 - related reduction reactions. Almost 100% of NO 2 can be removed in gaseous mixtures of N 2 +O 2 +H 2 O+NO 2 with negligible NO production.
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  • 18
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    Molecular and cellular biochemistry 194 (1999), S. 257-263 
    ISSN: 1573-4919
    Keywords: glycation ; oxidation ; collagen ; diabetes ; free radicals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The present investigation was carried out to understand the effect of metal catalyzed oxidation on glycation and crosslinking of collagen. Tail tendons obtained from rats weighing 200-225 g were incubated with glucose (250 mM) and increasing concentrations of copper ions (5, 25, 50 and 100 μM) under physiological conditions of temperature and pH. Early glycation, crosslinking and late glycation (fluorescence) of collagen samples were analyzed periodically. Early glycation was estimated by phenol sulfuric acid method, and the crosslinking was assessed by pepsin and cyanogen bromide digestion. A concentrationdependent effect of metal ions on the rate of glycation and crosslinking of collagen was observed. Tendon collagen incubated with glucose and 100 μM copper ions showed 80% reduction in pepsin digestion within seven days, indicating extensive crosslinking, whereas collagen incubated with glucose alone for the same period showed only 7% reduction. The presence of metal ions in the incubation medium accelerated the development of Maillard reaction fluorescence on collagen, and the increase was dependent on the concentration of metal ions used. The metal chelator Diethylene triamine penta-acetate significantly prevented the increase in collagen crosslinking by glucose and copper ions. Free radical scavengers benzoate and mannitol effectively prevented the increased crosslinking and browning of collagen by glucose. The results indicate that the metal catalyzed oxidation reactions play a major role in the crosslinking of collagen by glucose. It is also suggested that the prevention of increased oxidative stress in diabetes may prevent the accelerated advanced glycation and crosslinking of collagen.
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  • 19
    ISSN: 1573-4889
    Keywords: oxidation ; segregation ; impurities ; CeO2-coated Fe-20Cr
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interfacial segregation of sulphur and carbon during the oxidation in 1 torr O2 at 1173 K of Fe-20Cr alloy, which was either free of Ce, alloyed with 0.078 wt.% Ce, or sputter-coated with a 4 nm-thick CeO2 layer, was studied using polyatomic SIMS. Oxidation periods were up to 19 hr. During oxidation, sulphur and carbon accumulated at the alloy-oxide interface region of both uncoated and coated alloys. The amount of segregated sulphur did not vary appreciably with time, whereas carbon increased with time. The total amount of segregants was similar for both uncoated and coated alloys, although the scales formed on the sputter-coated alloy maintained adhesion and were about 10 times thinner than those on the uncoated alloys.
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  • 20
    ISSN: 1573-4889
    Keywords: Incoloy 800H ; oxidation ; sulphidation ; ion implantation ; CER
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Coatings, obtained by preoxidation of Incoloy 800H at low PO2 show good sulphidation resistance due to the higher chromia content in the oxide scale. Yttrium-ion implantation of Incoloy 800H has also a beneficial effect on sulphidation, if preoxidation is applied. The reason for this is presumably the segregation of yttrium to grain boundaries of the oxide. Furthermore, the oxidation kinetics of Incoloy 800H are independent of the partial pressure of the oxygen. Mechanical testing of the preformed oxide scale/substrate combinations in air at 600°C by means of constant-extension-rate experiments shows that preoxidation at low partial pressures of oxygen leads to earlier scalecracking.
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  • 21
    ISSN: 1573-4889
    Keywords: oxidation ; sulphur ; manganese ; silicium ; precipitate ; cracks
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation of presulphidized Ni-Cr alloys has been studied by taking into account the influence of the two distinct oxidation mechanisms described in part I of this article. Sulphur enters the Cr2O3 scale (in Ni-34Cr alloys) mainly as S2− species, which at high temperatures increases the V‴Cr content, and hence the oxidation kinetics. Sulphur is randomly distributed in the scale, except at the inner oxide-alloy interface, where intergranular microsulphides are analyzed in the oxide-scale zone. In the case of NiO, NiCr2O4, Cr2O3 oxide multilayers (in a Ni-20Cr alloy), sulphur in the S2− state is distributed in the oxide layers or at Si-precipitate interfaces. Such a distribution leads to crack formation, especially during cooling.
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  • 22
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    Oxidation of metals 33 (1990), S. 301-308 
    ISSN: 1573-4889
    Keywords: Pb-In alloys ; oxidation ; oxide-inversion layer ; Auger analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation of several single-phase Pb-In alloys has been studied in air at room temperature using AES (Auger electron spectroscopy) combined with sputter-depth profiling. Alloy samples with indium composition between 3 and 64 at.% In, which were prepared using a microtome, were oxidized in air. The oxidation of alloys with low In contents was found to be the same as that of Pb-2.9 at.% Sn.1 Increasing the bulk composition of In increased the ratio of oxidized In to oxidized Pb in the oxide mixture, although Pb oxide was observed even on the surface of the oxide for samples up to 64 at.% In. The oxidation behavior of Pb-In alloys can be explained in terms of preferential oxidation of In due to its much greater affinity for oxygen than Pb.
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  • 23
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    Oxidation of metals 34 (1990), S. 47-70 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; angle of incidence ; nickel ; cobalt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The combined erosion-oxidation of cobalt and nickel at 600 and 780°C over a range of particle-impact angles has been studied by using weight change vs. time measurements and extensive morphological and microstructural characterization of exposed specimens. The oxidation process has been found to affect the angular dependence of the degradation rates. The effect is especially significant at low-impact angles where ripples and flakes are developed upon the surfaces of specimens.
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  • 24
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    Oxidation of metals 34 (1990), S. 465-472 
    ISSN: 1573-4889
    Keywords: Al-Mg alloys ; oxidation ; MgO layers ; growth mechanism ; oxide morphology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation of Al-5Mg alloy has been studied at 550°C in dry air. Morphological details of the MgO layers which develop on this alloy during hightemperature oxidation have been studied by scanning electron microscopy (SEM). A localized detachment of the protective, adherent MgO layer was found, which is caused by voids formed by vacancy condensation at the metal-oxide interface. The source of these vacancies was the outward diffusion of Mg through the oxide layer. Continuing growth of these voids was responsible for cracking of oxide ridges and nodules, as well as the growth of new MgO having a “cauliflower” morphology. A model describing the process of the outward diffusion is given.
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  • 25
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    Molecular and cellular biochemistry 95 (1990), S. 177-182 
    ISSN: 1573-4919
    Keywords: periodate ; oxidation ; membrane ; cells ; interleukin-1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Interleukin-1 (IL-1) production by periodic acid (H5IO6)-oxidized human peripheral blood mononuclear (PBMN) cells was assessed by the thymocyte co-mitogenesis assay. Maximum IL-1 levels (∼ 1.2 U/ml) in the conditioned media of PBMN cells were registered within the first 24 hrs post-oxidation, whereas no IL-1 was detected in the media from 24 hrs control cultures. Thymocyte proliferation, driven by periodic acid-induced IL-1, was abolished by an antibody to IL-1alpha and IL-1β. Quantitative analysis of IL-1-containing medium by radioimmunoassay (RIA) indicated that IL-1β comprised about 80% of total IL-1. Partial characterization of H5IO6-induced IL-1β indicated that it was identical to IL-1 produced by lipopolysaccharide-stimulated macrophages. It is concluded that oxidation of human PBMN cells by H5IO6 triggers synthesis and release of IL-1, most of which was in its IL-1β form.
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  • 26
    ISSN: 1573-4889
    Keywords: oxidation ; carbon ; manganese ; nickel ; silicon ; Ni-Cr alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation behavior of Ni-Cr alloys (34 and 20 wt.% Cr) was investigated between 850 and 1200°C in oxygen for a maximum duration of about 70 hr. The oxide-growth mechanism is a diffusion process controlled by either outward diffusion of chromium in Cr2O3 (Ni-34Cr alloy) or by an increase in grain size (Ni-20Cr alloy). In the case of the Ni-34Cr alloy, low values of chromium diffusion were found for the growth of Cr2O3 by taking into account the general equation of Wagner. The influence of impurities (Si, C, Mn, Ni) diffusing from the underlying alloy is analyzed because of their doping effect in the outer oxide scales.
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  • 27
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    Oxidation of metals 34 (1990), S. 23-45 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; high-temperature corrosion ; interactions ; nickel ; cobalt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The combined erosion-oxidation of nickel, cobalt, and the oxides of these metals have been studied at 780°C in air to examine two regimes of interactionnamely, a regime of erosion-enhanced oxidation during which an oxide scale of constant thickness covers metal specimens, and a regime of oxidation-affected erosion that is characterized by a composite surface layer of metal, oxide, and erodent. In the case of cobalt, these two regimes have been documented and the transition from one regime to another described. For the range of conditions examined, only the oxidation-affected erosion regime was observed for nickel due to its lower oxidation rate compared to cobalt.
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  • 28
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    Oxidation of metals 34 (1990), S. 217-228 
    ISSN: 1573-4889
    Keywords: pack Cementation ; titanium aluminides ; activator ; diffusion ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The practical application of titanium aluminide metal-matrix composites (MMCs) at high temperatures requires suitable surface coatings to provide the needed oxidation resistance. Without a coating, the titanium aluminide alloys suffered from rapid oxidation attack at elevated temperatures, particularly under thermal cyclic conditions. The pack-cementation coating process was utilized to aluminize the surface region of a Ti3Al-base alloy to TiAl3, the most oxidation-resistant phase. With the existence of an adherent conversion coating, a thin protective alumina scale formed on the outer surface, and a significant improvement in the corrosion resistance was observed. Excellent coating efficiency and geometric flexibility were demonstrated in this study by the pack-cementation technique. Further development of the cementation process will focus on the elimination of surface cracking in the coating.
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  • 29
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    Oxidation of metals 34 (1990), S. 229-258 
    ISSN: 1573-4889
    Keywords: nickel ; oxidation ; oxygen tracer ; SIMS ; duplex scale
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The effect of oxidation conditions on the penetration of oxygen into growing nickel oxide scales has been examined using oxygen isotope tracers and SIMS analysis. Depth profiles and cross-section images of oxide scales show that the proportion of oxygen penetration is increased as the temperature is reduced. At 600°C, the amount of oxygen tracer transported to the scale-metal interface is considerable, approaching that observed for a conventional “duplex” microstructure. The formation of healing oxide along numerous fissures through the oxide is directly observed in SIMS images. These fissures seem to coincide with grain boundaries in the preexisting oxide. As the oxidation temperature is increased, the oxygen transport becomes less uniform, some regions of the scale showing little or no transport. Reduction in the oxygen pressure reduces the amount of oxygen penetrating the scale.
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  • 30
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    Oxidation of metals 34 (1990), S. 323-333 
    ISSN: 1573-4889
    Keywords: Al-Mg alloys ; oxidation ; high-temperature mechanisms
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Surface-analysis techniques (x-ray photoelectron spectroscopy and Auger electron spectroscopy) and electron microscopy (SEM and TEM) have been used to study the mechanism of steady-state high-temperature oxidation of Al-Mg alloys. Two high-purity alloys containing 0.4 and 2.0 wt.% Mg were heat-treated in dry air at 550°C up to 90 hr. It was found that the oxide layer was composed of MgO and spinel (MgAl2O4), the major constituent being MgO. The molar concentration of MgO decreased with increasing depth, while that of spinel increased. The rate-controlling mechanism for the growth of the oxide layer in the Al-0.4Mg alloy was the solid-state diffusion of Mg in the MgO-spinel constituents. For alloys of higher-magnesium content, the growth of the oxide layer was controlled by solid-state diffusion of Mg through the adherent protective oxide areas and by the transport of Mg vapor across voids formed between the alloy substrate and the oxide layer.
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  • 31
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    Oxidation of metals 33 (1990), S. 1-17 
    ISSN: 1573-4889
    Keywords: Ni-Cr-Al alloys ; alloy microstructure ; oxidation ; refractory-metal additions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation behavior at 1023 and 1123 K in air has been followed for several Ni-Cr-Al ternary alloys and with small additions of refractory elements Nb, Mo, and Ta. Prior to testing, the alloys were characterized by microscopic and microanalytic methods. Microstructural observations have shown that the formation of oxide layers depends on the original microstructure. Discontinuous thermogravimetric tests were used to relate the behavior of different chromium, aluminum, and refractory-element additions, and eventually to service conditions in similar environments in which general oxidation takes place. The addition of refractory elements generally impaired the oxidation resistance.
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  • 32
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    Oxidation of metals 33 (1990), S. 309-320 
    ISSN: 1573-4889
    Keywords: manganese steels ; aluminum coatings ; oxidation ; thermogravimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Austenitic Mn-Al alloys (20–32 W/O Mn, 7–10 Al, 2–3 Si, 1C) were found to have satisfactory oxidation resistance up to 950°C under isothermal conditions in air. Surface enrichment of aluminum is a necessary condition for obtaining an almost pure alumina scale for uses at higher temperatures. Four different Mn-steels were Al-coated by the Capuano electroplating process. In all the steels there was an increase in the hot-oxidation resistance. The best results were obtained with steels containing both Al and Si, and this for temperatures up to 1100°C. No spalling was noticed during rapid cooling of the test pieces. Silicon was found to act as a diffusion barrier to outward iron diffusion. It appears that there is formation of a pure, thin film of alumina from the matrix which interacts with the aluminum diffusing from the superimposed, coating for the formation of good bonds.
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  • 33
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    Molecular and cellular biochemistry 200 (1999), S. 103-109 
    ISSN: 1573-4919
    Keywords: sugar cataract ; dulcitol ; glycation ; oxidation ; pyruvate ; ethyl pyruvate ; attenuation effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Studies describe an attenuation of sugar cataract formation by topical administration of ethyl pyruvate. Cataract formation was induced by feeding young rats a 30% galactose diet. Mature cataracts appeared in about thirty days. Instillation of the eye drops containing 5% ethyl pyruvate decelerated the process significantly. Biochemically, the effect was reflected by lowering in the contents of dulcitol and glycated proteins. The ATP levels were also higher in comparison to the placebo treated group. The effects are hence attributable to the effect of pyruvate in inhibiting dulcitol synthesis and protein glycation, in addition to its antioxidant properties and metabolic support. The use of esterified pyruvate instead of the unesterified pyruvate was preferred because of its greater penetration through the cornea and consequently a higher concentration attained in the aqueous humor.
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  • 34
    ISSN: 1572-9028
    Keywords: ellipsometry ; carbon monoxide ; methane ; palladium ; palladium oxide ; oxidation ; oscillations ; catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Spectroscopic ellipsometry is used to monitor the surface of a thick Pd‐film catalyst during the oxidation of either carbon monoxide or methane. Dense PdO layers form under sufficiently lean conditions (excess oxygen) for both reactions. A stable metal surface exists in the case of CO, but a very porous PdO layer develops in the case of methane, under rich conditions. There is a large hysteresis in the conditions for PdO formation in the case of CO oxidation. Spontaneous oscillations in catalytic activity and Pd‐surface composition occur for both reactions, the higher activities corresponding to O‐atom‐rich or PdO‐rich surfaces for CO or methane oxidation, respectively.
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  • 35
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    Topics in catalysis 8 (1999), S. 45-55 
    ISSN: 1572-9028
    Keywords: Raman spectroscopy ; surface‐enhanced Raman spectroscopy ; oxidation ; synergy effects ; oxygen exchange ; oxidative coupling of methane ; nitric oxide decomposition ; methanol oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Advantages and limitations of laser Raman spectroscopy (LRS) as an in situ vibrational spectroscopy for the study of catalytic materials and surfaces under working conditions are discussed. Measurements can be carried out at temperatures as high as 1200 K in controlled atmospheres. Modern instrumentation permits time resolutions in the sub‐second regime for materials with high Raman cross sections. Transient studies are thus possible. Several examples are presented of in situ LRS studies including the phase analysis of bismuth molybdate and VPO oxidation catalysts, synergy effects and oxygen exchange in Sb2O3/MoO3 oxide mixtures, intermediates in oxidative coupling of methane, NO decomposition on Ba/MgO catalysts, and transient SERS studies of partial oxidation of methanol on Ag single crystal surfaces and of the reduction of oxide overlayers on electrodeposited Rh layers.
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  • 36
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    Oxidation of metals 33 (1990), S. 177-189 
    ISSN: 1573-4889
    Keywords: kinetics ; oxidation ; titanium hydride ; rutile
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation kinetics of titanium-hydride powders were studied in the temperature range of 298–1378 K in air at atmospheric pressure. DTA, DSC, X-ray analysis, and scanning electron microscopy were used. Oxidation was found to take place by TiHxOy oxyhydride phases formation. The oxidation reaction rate at temperatures above 870 K was limited by diffusion of oxygen atoms through a rutile scale formed on the surface. The activation energy and preexponential values of the Arrhenius equation for different interaction stages as well as transformation enthalpies were calculated.
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  • 37
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    Oxidation of metals 33 (1990), S. 157-176 
    ISSN: 1573-4889
    Keywords: Fe-Ni-G-Al-S ; alloys ; Mo and Mn additions ; oxidation ; chromic scales
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Oxidation tests were conducted on a master alloy, Fe-16Ni-(5–8)Cr-3Si-lA1, to which (0–4) wt/o pct Mn and/or Mo were added. Tests were conducted at temperatures ranging from 1073–1273 K for times up to 1000 hr. Additions of Mn resulted in formation of a dual oxide structure and decreased oxidation protection. Addition of Mo significantly improved oxidation protection by formation of an intermetallic Fe(Mo)Si precipitate that eventually formed a protective SiO2 oxide sublayer. Increasing the Cr concentration in an alloy containing both Mn and Mo resulted in a slight increase in weight gain. To first order, the apparent oxidation activation energy for all the alloys was nearly constant, 121 kJ/mol, suggesting that the same mechanism controlled the oxidation for all compositions. The oxidation protection was related to the alloy components and concentration.
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  • 38
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    Oxidation of metals 33 (1990), S. 481-508 
    ISSN: 1573-4889
    Keywords: Fe-Cr-Al-Y ; yttrium ; sulfidation ; oxidation ; diffusion ; mixed gas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The effects of 1 wt. % yttrium addition to an iron-base model alloy, Fe-25Cr-6Al, on the scale formation and breakdown mechanisms in a mixed gas at temperatures 500–700°C were studied. In this environment, the equilibrium gas contained sulfur and oxygen at high and low vapor pressures, respectively. During the exposure, the formation of an alumina scale was favored kinetically on the surfaces of the alloys. The oxide scale formed on the base (Y-free) alloy had a fine-grained structure which exhibited excellent sulfidation/oxidation resistance. However, because of severe segregation along the grain-boundaries of the Y-containing alloy, which resulted in second-phase precipitation rich in Fe and Y, the morphology of the surface oxide on this alloy exhibited a distinction along the wide substrate grain boundaries. These Fe- and Y-rich regions served as short circuits for Fe diffusion from the underlying substrate to the scale/gas interface and, eventually, allowed iron sulfide to form on the oxide scale. With a pre-oxidation treatment, the transient stage from oxidation to sulfidation was prolonged; however, the sulfidation process was not eliminated. Based on thermodynamic calculations, the probable phases forming on the alloy surface in the oxidizing/sulfidizing environment were predicted, and a qualitative model for the corrosion mechanisms was proposed.
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  • 39
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    Oxidation of metals 34 (1990), S. 71-100 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; alloys interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The modes of interaction of erosion and high-temperature oxidation, occurring simultaneously on an alloy surface, have been studied using Ni-30Cr, MA754, Ni-20Al, and Co-22Cr-11Al-0.2Y alloys to examine the influence of chromia and alumina scale formation on the erosion of nickel and cobalt base alloys. The results have shown that, in the presence of a rapidly flowing oxidizing gas stream, the evaporation of volatile metal oxides becomes important at lower temperatures where normally it can be ignored. Otherwise, the erosion and oxidation of alloys parallels the behavior of pure metals but also introduces additional factors derived from lengthening of the period of transient oxidation and modification of concentration profiles in the alloy adjacent to the alloy/scale interface. Higher erosion intensities extend the transient oxidation behavior which adversely affects the formation of protective scales. As with pure metals, the presence of erosion and oxidation together always produced increased rates of degradation.
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  • 40
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    Oxidation of metals 34 (1990), S. 497-528 
    ISSN: 1573-4889
    Keywords: oxidation ; sulfidation ; mixed-gas environment ; oxide-dispersion-strengthened alloy ; yttria addition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract High-temperature oxidation and sulfidation studies were conducted on an oxide-dispersion-strengthened alloy of composition Fe-20Cr-16Ni-4Al-1Y2O3. The oxidation studies were conducted in air and low-PO2 environments over a temperature range of 650–1200°C. Results are also reported on the sulfidation resistance of preformed oxide scales and the influence of reoxidation of preformed sulfide scales. Detailed microstructural results and x-ray diffraction analysis data are presented to substantiate the corrosion behavior of the alloy over the wide range of conditions anticipated in fossil-energy systems. Data are also presented on the corrosion behavior of the alloy in oxygen/sulfur mixed gas atmospheres, and the results are used to compare the corrosion behavior of the present alloy with other chromia- and alumina-forming alloys.
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  • 41
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    Journal of sol gel science and technology 14 (1999), S. 75-86 
    ISSN: 1573-4846
    Keywords: silicon oxycarbide ; BlackglasTM ; ceramic matrix composites ; 29Si NMR ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract BlackglasTM polysiloxane systems produce silicon oxycarbide glasses by pyrolysis in inert atmosphere. The silicon oxycarbides evidence oxidative degradation that limits their lifetime as composite matrices. The present study characterizes bonding rearrangements in the oxycarbide network accompanying increases in pyrolysis temperature. It also addresses the changes in susceptibility to oxidation due to variations in the distribution of Si bonded species obtained under different processing conditions. The study is carried out using 29Si nuclear magnetic resonance (NMR) spectroscopy and a design of experiments approach to model the oxidation behavior. The NMR results are compared with those obtained by thermogravimetric analysis (TGA). Samples pyrolyzed under inert conditions are compared to those pyrolyzed in reactive ammonia environments.
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  • 42
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    Journal of sol gel science and technology 14 (1999), S. 49-68 
    ISSN: 1573-4846
    Keywords: silicon oxycarbide ; oxidation ; silsesquioxane ; preceramic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract We have undertaken a systematic study of the oxidation chemistry for a range of SiOC ceramics derived from silsesquioxane polymeric precursors. This study examines the oxidation for 500 hours at 600, 800, 1000 and 1200°C for four SiOC powders. The material changes upon oxidation were characterized qualitatively by color change and optical microscopy and quantitatively by weight and composition change. In this study we employ a very easy method that uses the weight change upon oxidation and a carbon analysis after oxidation to arrive at the composition of the oxidized SiOC. Combined these qualitative and quantitative techniques have shown that on oxidation at 800 and 600°C the SiOC composition is more rapidly changed to that of silica than oxidation over the same time frame at 1000 or 1200°C. The data indicates that this difference is due to the relative rates of oxidation of the excess carbon versus the Si—C bonds in the SiOC. At lower temperatures initially the carbon oxidation predominates which leads to higher porosity throughout the material and an increase in the surface area with eventually ‘complete’ oxidation to silica. At higher temperatures the Si—C bond oxidation rate is comparable to the rate of oxidation of carbon. This allows a silica-like surface to build up on the SiOC, which slows all subsequent reactions due to the necessity to diffuse O2 in and COx out of the bulk. Under these oxidation conditions materials that originally contain high amounts of excess carbon are more quickly oxidized to silica than those that contain minimal amounts of excess carbon, as confirmed by elemental analysis and optical microscopy. Regardless of the time or temperature of the oxidation conditions no materials were found to be completely stable to oxidation. SiOC materials with low levels of excess carbon showed the best resistance to change upon oxidation.
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  • 43
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    Physics and chemistry of minerals 26 (1999), S. 506-512 
    ISSN: 1432-2021
    Keywords: Key words Anapaite ; Mössbauer spectroscopy ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Mössbauer spectra (MS) of anapaite (Ca2 Fe2+(PO4)2 · 4H2O) and of a sample after being immersed in a 4% H2O2 solution at room temperature (RT) over 12 days (hereafter an4ox) were collected at temperatures in the range 4.2 to 420 K and 11 to 300 K respectively. All MS consist of symmetrical doublets, hence magnetic ordering was not observed. The temperature dependencies of the Fe2+ centre shifts of anapaite and an4ox were analysed with the Debye model for the lattice vibrations. The characteristic Mössbauer temperatures were found as 370 K ± 25 K and 340 K ± 25 K, and the intrinsic isomer shifts as 1.427 ± 0.005 mm/s and 1.418 ± 0.005 mm/s respectively. From the external-field (60 kOe) MS recorded at 4.2 and 189 K for the non-treated sample, the principal component V zz of the electric field gradient (EFG) is determined to be positive and the asymmetry parameter η ≈ 0.2 and 0.4 respectively. The temperature variations of the quadrupole splittings, ΔE Q(T), cannot be interpreted on the basis of the thermal population of the 5 D electronic levels resulting from the tetragonal compression of the O6 co-ordination. The low-temperature linear behaviour of ΔE Q(T) is attributed to a strong orbit-lattice coupling. A field of 60 kOe applied to anapaite at 4.2 K produces magnetic hyperfine splitting with effective hyperfine fields of −136, −254 and −171 kOe along the principal axes Ox, Oy and Oz of the EFG tensor respectively. Additional oxidation treatments in solutions with various H2O2 concentrations up to 20% and subsequent Mössbauer experiments at room temperature, have revealed that the anapaite structure is not sensitive to oxidation since eventually only a small amount of Fe2+ (∼6.5%) is converted into Fe3+.
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    The journal of membrane biology 118 (1990), S. 153-159 
    ISSN: 1432-1424
    Keywords: sulfhydryls ; N-ethylmaleimide ; oxidation ; carbethoxylation ; diethylpyrocarbonate ; hydroxylamine ; sheep red blood cells ; K∶Cl cotransport ; ATP ; GSH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Hydroxylamine, a potent oxidizing agent used to reverse carbethoxylation of histidine by diethylpyrocarbonate, activated Cl-dependent K flux (K∶Cl cotransport) of low K sheep red blood cells almost sixfold. When K∶Cl cotransport was already stimulated by N-ethylmaleimide, hydroxylamine caused an additional twofold activation suggesting modification of sites different from those thiol alkylated. This conclusion was supported by the finding that hydroxylamine additively augmented also the diamide-induced K∶Cl flux (Lauf, P.K. 1988.J. Membrane Biol. 101:179–188) with dithiothreitol fully reversing the diamide but not the hydroxylamine effect. Stimulation of K∶Cl cotransport by hydroxylamine was completely inhibited by treatment with diethylpyrocarbonate also known to prevent K∶Cl cotransport stimulation by N-ethylmaleimide, both effects being independent of the order of addition. Hence, although the effect of carbethoxy modification on K∶Cl flux cannot be reversed by hydroxylamine and thus excludes histidine as the target for diethylpyrocarbonate, our finding reveals an important chemical determinant of K∶Cl cotransport stimulation by both hydroxylamine oxidation and thiol group alkylation.
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  • 45
    ISSN: 1572-8978
    Keywords: Plasma polymers ; oxidation ; XPS ; photoelectron binding energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Technology
    Notes: Abstract The incorporation of oxygen into nitrogen-containing plasma deposited polymers was studied by X-ray Photoelectron Spectroscopy (XPS). As the oxygen content of the plasma polymer increased, the binding energy of the N 1s photoelectrons increased. Conversely, the binding energy of the O 1s photoelectrons was inversely proportional to the nitrogen content of the plasma polymer. The data from a large number of samples all obeyed the same “universal” correlations of photoelectron binding energy versus chemical composition. The data were described by the same curve regardless of whether the oxygen was incorporated rapidly into the thin film during plasma deposition or whether the oxygen was added slowly during spontaneous oxidation of the film in air. This implies that the same thermodynamic principles of radical reactions governed the addition of oxygen to the plasma polymer. The shift in the O 1s and N 1s photoelectron binding energies as a function of chemical composition was used to monitor the proximity of nitrogen and oxygen. By contrasting the experimental data with a simple binomial model which described the random addition of oxygen to a lattice containing carbon and nitrogen, we were able to show that oxygen was preferentially added near nitrogen-containing groups in plasma polymers.
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  • 46
    ISSN: 1573-5036
    Keywords: Gaeumannomyces graminis ; genotypes ; interaction ; manganese ; oxidation ; take-all ; Triticum aestivum ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Take-all is a world-wide root-rotting disease of cereals. The causal organism of take-all of wheat is the soil-borne fungus Gaeumannomyces graminis var tritici (Ggt). No resistance to take-all, worthy of inclusion in a plant breeding programme, has been discovered in wheat but the severity of take-all is increased in host plants whose tissues are deficient for manganese (Mn). Take-all of wheat will be decreased by all techniques which lift Mn concentrations in shoots and roots of Mn-deficient hosts to adequate levels. Wheat seedlings were grown in a Mn-deficient calcareous sand in small pots and inoculated with four field isolates of Ggt. Infection by three virulent isolates was increased under conditions which were Mn deficient for the wheat host but infection by a weakly virulent isolate, already low, was further decreased. Only the three virulent isolates caused visible oxidation of Mn in vitro. The sensitivity of Ggt isolates to manganous ions in vitro did not explain the extent of infection they caused on wheat hosts. In a similar experiment four Australian wheat genotypes were grown in the same Mn-deficient calcareous sand and inoculated with one virulent isolate of Ggt. Two genotypes were inefficient at taking up manganese and were very susceptible to take-all, one was very efficient at taking up manganese and was resistant to take-all, and the fourth genotype was intermediate for both characters. All genotypes were equally resistant under Mn-adequate conditions.
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  • 47
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    Journal of chemical ecology 25 (1999), S. 611-628 
    ISSN: 1573-1561
    Keywords: Terrestrial isopods ; Oniscidea ; Porcellio scaber ; phenolics ; hydrolysis ; oxidation ; detoxification ; hindgut cuticle ; gut microbiota ; hepatopancreatic bacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract When adults of Porcellio scaber fed on litter prior to an artificial diet containing 5% of commercially available tannic acid, 55% of the ingested galloylglucose esters was excreted unchanged, about 25% was hydrolyzed, and 20% was oxidized during the gut passage. After reducing the counts of microorganisms in the gut of P. scaber, the data obtained indicated an important role of ingested platable microorganisms in hydrolyzing gallotannins. Oxidation of phenolics appeared to be mainly due to the endosymbiotic bacteria of the hepatopancreas. Microbial counts in the hindgut were strongly reduced by ingested galloylglucose esters, while gallic acid in the diet (2%) reduced the number of palatable fungi and bacteria less strikingly, and increased the total number of the gut microbiota. Hepatopancreatic bacteria were only slightly affected by ingested tannic acid, since the hepatopancreas contained only few galloylglucose esters. This may be due to the permeability of the hindgut cuticle: the cuticle of the anterior hindgut was freely permeable to gallic acid, while it was nearly impermeable to larger polyphenols. The cuticle of the posterior hindgut was permeable to only about 4% of the gallic acid present in the hindgut lumen. The results are discussed with respect to potentially harmful effects of ingested hydrolyzable tannins and their digestion in Porcellio scaber.
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  • 48
    ISSN: 1573-0867
    Keywords: elemental sulphur ; oxidation ; organic S ; mineralization ; immobilization ; S fertilizers ; semiarid soils ; subtropical region
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The increasing sulphur (S) deficiency in soils of several parts of world has led to the use of fertilizer S, an important factor in enhancing the production and quality of crops. Very limited information is available on the use of elemental sulphur (S0) as a fertilizer, its oxidation into SO42- and transformation into organic S in semiarid subtropical soils. We studied the impact of three temperature regimes on the mineralization of soil organic S, and the oxidation and immobilization of S0 in acidic (pH 4.9), neutral (pH 7.1) and alkaline (pH 10.2) subtropical soils of north-western India. Repacked soil cores were incubated under aerobic conditions (60% water-filled pore space) for 0, 14, 28 and 42 d with and without incorporated S0 (500 μg g-1 soil). Temperature had profound effects on all three soils processes, the rates of mineralization of native soil organic S, oxidation of applied S0 and transformation of S0 into soil organic S being greatest at 36 °C, irrespective of soil pH. Mineralization of native soil organic S (without added S0) resulted in the accumulation of 39, 66 and 47 μg SO42-–S g-1 soil in acidic, neutral and alkaline soil in 42 d period at 36 °C. Of the total mineralization, the majority (62 – 74%) occurred during the first 14 d period. Oxidation rate of added S0 during initial 14 d period at 36 °C was highest in alkaline soil (292 μg S cm-2 d-1), followed by neutral soil ((180 μg S cm-2 d-1) and lowest in acidic soil (125 μg S cm-2 d-1). Of the applied 500 μg S0 g-1 soil, 3.2 – 10.0%, 6.8 – 15.4% and 10.0 – 23.0% oxidized to SO42-, and 13.4 – 28.6%, 16.0 – 29.0% and 14.6 – 29.0% were transformed into organic S in 42 d period in acidic, neutral and alkaline soil, respectively. The results of our study suggest that in order to synchronize the availability of S with plant need, elemental S may be applied well before the seeding of crops, especially in acidic soil and in regions where temperature remains low. Substantial mineralization of native soil organic S in the absence of applied S0 and immobilization of applied S0 into organic S suggest that the role of soil biomass as source and sink could be exploited in long term S management.
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  • 49
    ISSN: 1572-9729
    Keywords: Diphenyl ether ; ligninolytic enzymes ; metabolites ; oxidation ; Trametes versicolor ; white-rot fungi
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The white-rot fungi Trametes versicolor SBUG 1050, DSM 11269 and DSM 11309 are able to oxidize diphenyl ether and its halogenated derivatives 4-bromo- and 4-chlorodiphenyl ether. The products formed from diphenyl ether were 2- and 4-hydroxydiphenyl ether. Both 4-bromo- and 4-chlorodiphenyl ether were transformed to the corresponding products hydroxylated at the non-halogenated ring. Additionally, ring-cleavage products were detected by high perfomance liquid chromatography and characterized by gas chromatography/mass spectrometry and proton nuclear magnetic resonance spectroscopy. Unhalogenated diphenyl ether was degraded to 2-hydroxy-4-phenoxymuconic acid and 6-carboxy-4-phenoxy-2-pyrone. Brominated derivatives of both these compounds were formed from 4-bromodiphenyl ether, and 4-chlorodiphenyl ether was transformed in the same way to the analogous chlorinated ring cleavage products. Additionally, 4-bromo- and 4-chlorophenol were detected as intermediates from 4-bromo- and 4-chlorodiphenyl ether, respectively. In the presence of the cytochrome-P450 inhibitor 1-aminobenzotriazole, no metabolites were formed by cells of Trametes versicolor from the diphenyl ethers investigated. Cell-free supernatants of whole cultures with high laccase and manganese peroxidase activities were not able to transform the unhydroxylated diphenyl ethers used.
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  • 50
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    Journal of thermal analysis and calorimetry 55 (1999), S. 681-690 
    ISSN: 1572-8943
    Keywords: chromia ; Fe-Cr alloy ; gas-solid reaction kinetics ; H2/H2O gas mixtures ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The high-temperature oxidation behavior of a ferritic alloy (SUS 430) in a SOFC environment, corresponding to the anode (H2/H2O gas mixture) and cathode (air) operating conditions, was determined with regard to application of the alloy as a metallic separator material in SOFC. The oxidation kinetics of Fe-16Cr alloy (SUS 430), was studied by thermogravimetry in H2/H2O gas mixtures with pH/pHO=94/6 and 97/3 and in air, in the temperature range 1023-1223 K, for 3.6 up to 1080 ks. It was found that the protective oxide scale, composed mainly of Cr2O3 with uniform thickness and excellent adhesion to the metal substrate, grows in accordance with the parabolic rate law. The dependence of the parabolic rate constant, kp, of the scale on temperature obeys the Arrhenius equation: kp=6.8×10-4 exp (-202.3 kJ mol-1R-1T-1) for H2/H2O gas mixtures with pH/pHO=94/6. The determined kp was independent of the oxygen partial pressure in the range from 5.2×10-22 to 0.21 atm at 1073 K, which means that the rates of growth of the scale on Fe-16Cr alloy in the above-mentioned atmospheres are comparable. The oxidation test results on Fe-16Cr alloy in H2/H2O gas mixtures and air demonstrate the applicability of SUS 430 alloys as a separator for SOFC.
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    Journal of thermal analysis and calorimetry 55 (1999), S. 981-987 
    ISSN: 1572-8943
    Keywords: nickel phosphates ; nickel phosphides ; Ni-P alloys ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract DTA in conjuction with X-ray diffraction analysis with a high-temperature camera and infrared spectroscopy was employed to determine the mechanism of oxidation of Ni-P alloys. Amorphous Ni-P powders were obtained from a nickel(II) sulphate bath as a nickel source and sodium dihydrophosphate(I) as a reducing agent. The crystallization product is composed of two phases: (f.c.c.) Ni and (b.c.t.) Ni3P. The amorphous to crystalline transformation takes place in the temperature range 280–330°C. Ni3P samples were heated from room temperature to 1050°C in air atmosphere at 5°C min−1. It was found that the first stage of oxidation of Ni3P goes through the intermediate phase of Ni12P5 formation to Ni2P. Some exothermic reactions were observed. Heating runs were interrupted after each reaction for crystal structure determination by IR spectrometry. Infrared spectra are reported and it is shown that the structure units present in the amorphous products at about 700°C were the oxoanions PO3 − and P2O7 −. The final products of the oxidation process are NiO and Ni3(PO4)2.
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  • 52
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    International journal of thermophysics 20 (1999), S. 299-308 
    ISSN: 1572-9567
    Keywords: high temperature ; metal ; spectral emissivity ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The normal spectral emissivity and its time variation were measured systematically for a total of thirty kinds of pure metals and alloys at temperatures between 780 and 1200°C. The spectral data were obtained at about 100 wavelengths from 0.55 to 5.3 μm under different environmental conditions including oxidation. The spectral data were stored in a database with supplementary information on the specimens. Clear oscillations of the spectral emissivity with time and wavelength were observed for nickel, Inconel, and SUS444 as surface oxidation progressed, while emissivity variations were rather monotonic for other metals such as titanium, cold-rolled steel, and SUS310S. The surface roughness was measured for all specimens by a contact-type instrument before the measurements, and recorded as supplementary information in the database. The database was built on a personal computer operating system (Windows95) to facilitate the dissemination to researchers and engineers interested in the emissivity of metals. Indexes to the emissivity data are metal name, wavelength, temperature, time, and degree of oxidation represented by an effective thickness of oxide film on the specimen surface.
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    International journal of thermophysics 20 (1999), S. 289-298 
    ISSN: 1572-9567
    Keywords: high temperature ; metal ; spectral emissivity ; oxidation ; radiation thermometer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A system for measuring time variations of the normal spectral emissivity at wavelengths ranging from 0.55 to 5.3 μm was developed and applied to metal specimens in vacuum and oxidizing environments in the temperature range from 780 to 1200° C. The specimen was heated to high temperatures by passing a direct current in a vacuum chamber, and the surface oxidation was controlled by a low-pressure oxidizing gas. The specimen temperature was measured by a single-band (0.9-μm) radiation thermometer viewing at a cavity formed in the specimen from the rear side. The front surface of the specimen was observed by a multiband (112-wavelength) radiation thermometer to measure the normal spectral emissivity. The effective normal spectral emissivity of the specimen cavity was evaluated to be 0.94±0.05 at a wavelength of 0.9 μm in comparison with a metal tube having a small blackbody hole on the rear. The measurement uncertainty of the normal spectral emissivitiy by the system was estimated to be 5 to 10% of the emissivity value in most of the interesting ranges of emissivities, temperatures, and wavelengths.
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  • 54
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    Cellular and molecular neurobiology 19 (1999), S. 533-552 
    ISSN: 1573-6830
    Keywords: benzodiazepines ; cytochromes P450 ; oxidation ; reduction ; conjugation ; drug interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1. The benzodiazepines are among the most frequently prescribed of all drugs and have been used for their anxiolytic, anticonvulsant, and sedative/hypnotic properties. Since absorption rates, volumes of distribution, and elimination rates differ greatly among the benzodiazepine derivatives, each benzodiazepine has a unique plasma concentration curve. Although the time to peak plasma levels provides a rough guide, it is not equivalent to the time to clinical onset of effect. The importance of α and β half-lives in the actions of benzodiazepines is discussed. 2. The role of cytochrome P450 isozymes in the metabolism of benzodiazepines and in potential pharmacokinetic interactions between the benzodiazepines and other coadministered drugs is discussed. 3. Buspirone, an anxiolytic with minimal sedative effects, undergoes extensive metabolism, with hydroxylation and dealkylation being the major pathways. Pharmacokinetic interactions of buspirone with other coadministered drugs seem to be minimal. 4. Zopiclone and zolpidem are used primarily as hypnotics. Both are extensively metabolized; N-demethylation, N-oxidation, and decarboxylation of zopiclone occur, and zolpidem undergoes oxidation of methyl groups and hydroxylation of a position on the imidazolepyridine ring system. Zopiclone has a chiral centre, and demonstrates stereoselective pharmacokinetics. Metabolic drug–drug interactions have been reported with zopiclone and erythromycin, trimipramine, and carbamazepine. Reports to date indicate minimal interactions of zolpidem with coadministered drugs; however, it has been reported to affect the C max and clearance of chlorpromazepine and to decrease metabolism of the antiviral agent ritonavin. Since CYP3A4 has been reported to play an important role in metabolism of zolpidem, possible interactions with drugs which are substrates and/or inhibitors of that CYP isozyme should be considered.
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    Cellular and molecular neurobiology 19 (1999), S. 133-140 
    ISSN: 1573-6830
    Keywords: Na/K-ATPase ; SH groups ; oxidation ; hydrogen peroxide ; hypochlorite ; antioxidants ; carnosine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1. Oxidative modification of Na/K-ATPase from brain and kidney has been studied. Brain enzyme has been found to be more sensitive than kidney enzyme to inhibition by both H2O2 and NaOCl. 2. The inhibition of Na/K-ATPase correlates well with the decrease in a number of SH groups, suggesting that the latter belong mainly to ATPase protein and are essential for the enzyme activity. We suggest that the differences in the number, location, and accessibility of SH groups in Na/K-ATPase isozymes predict their oxidative stability. 3. The hydrophilic natural antioxidant carnosine, the hydrophobic natural antioxidant α-tocopherol, and the synthetic antioxidant ionol as well as the ferrous ion chelating agent deferoxamine were found to protect Na/K-ATPase from oxidation by different concentrations of H2O2. The data suggest that these antioxidants are effective due to their ability to neutralize or to prevent formation of hydroxyl radicals.
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  • 56
    ISSN: 1573-2932
    Keywords: diffusion coefficient ; gaseous oxygen ; mine tailings ; oxidation ; water content
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract To evaluate the effectiveness of soil covers, column experiments were conducted on tailings protected by a three-layer soil cover and tailings directly exposed in the open laboratory for a period of 760 days. Periodic rain application was performed to simulate field conditions, and at four times during the experiments the pore water was completely flushed out of each column for analysis. Profiles of oxygen, temperature, and volumetric water content were measured throughout the experiment, and the post-testing pore water quality was also characterized. A one-dimensional semi-analytic diffusion model was used to simulate oxygen profiles in the uncovered tailings. Modelling performed using the geochemical code MINTEQ showed that in the laboratory, aluminium concentrations in the tailings pore water were controlled by Al(OH)SO4, sulphate by gypsum and Al(OH)SO4and iron by lepidocrocite in the upper half and by ferrihydrite in the lower half. In the field, however, the iron oxyhydroxide minerals formed in the oxidized zone appear to be dissolving. It was found that the cover was effective in preventing significant desaturation of the clay, even over a 150-day drying period. The covered tailings did not oxidize much during the experiments. In the uncovered tailings, oxygen modelling and examination of the geochemistry show that the rate of gross oxidation and the advancement of the oxidation front decreases with time. However, pore water quality is controlled by geochemical processes other than oxidation, as reported in the field.
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  • 57
    ISSN: 1588-2837
    Keywords: V2O5−ZrO2 catalyst ; oxidation ; o-xylene ; temperature stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract It has been established that at high temperatures (above 450°C) the V2O5−ZrO2 catalyst exhibits a higher selectivity in the oxidation ofo-xylene to phthalic anhydride than does the conventional V2O5−TiO2(a) catalyst. The catalyst selectivity is found to increase with respect to partial oxidation ofo-xylene, the valuable by-product maleic anhydride being obtained. Studies by different physicochemical methods have shown that V2O5−ZrO2 undergoes no significant phase and structural changes under high-temperature conditions.
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  • 58
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    Reaction kinetics and catalysis letters 66 (1999), S. 97-104 
    ISSN: 1588-2837
    Keywords: Heterogeneous catalysis ; oxidation ; temperature hysteresis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The temperature hysteresis observed in the oxidation of CO on both supported and unsupported catalysts can be explained by the local overheating of active centers rather than by transitions from one steady state to another.
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  • 59
    ISSN: 1588-2837
    Keywords: Catalyst ; ceramic foam ; molten salt ; Nox ; oxidation ; soot
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Diesel soot is combusted simultaneously by two reactions: combustion with NO2 and combustion with O2 with the aid of a molten salt catalyst. Both reaction pathways should always be considered to avoid misinterpretation of experimental data.
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    Reaction kinetics and catalysis letters 68 (1999), S. 285-289 
    ISSN: 1588-2837
    Keywords: Enthalpy ; chain propagation ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A calculation of the enthalpies of elementary steps of the intra- and intermolecular chain propagation for model oxidation reactions of ethers, esters, ketones and hydrocarbons has been carried out. The heats of the intermolecular and intramolecular transfer of free valence with participation of peroxy radicals and C−H bond of the oxygen-containing compounds are shown to be comparable.
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  • 61
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    Reaction kinetics and catalysis letters 68 (1999), S. 325-330 
    ISSN: 1588-2837
    Keywords: vitrification ; glass structure ; oxidation ; solid phase kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The capture of oxygen molecules by deep traps during oxygen diffusion in butanol glasses has been studied at 77 K as the kinetics of thetert-butyl radical oxidation. Slow glass formation in the samples increases the concentration of deep traps in the matrix. The total value of nonrelaxed free volume has no effect on the concentration of deep traps. It is assumed that trap formation is due to the formation of certain molecular structures below room temperature, most probably, with dissolved gas molecules.
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  • 62
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    Reaction kinetics and catalysis letters 66 (1999), S. 169-175 
    ISSN: 1588-2837
    Keywords: 1,3-pentadiene ; oxidation ; vanadyl ion ; HZMS-5
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Different methods and vanadium compounds have been used to carry out proton exchange of zeolite HZSM-5 by vanadium cations. The catalysts are characterized by specific surface area, XRD, IR spectroscopy and TPD of ammonia. The catalysts’ activity in the oxidation of 1,3-pentadiene and the selectivity to carbonyl compounds are compared.
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    Reaction kinetics and catalysis letters 66 (1999), S. 63-70 
    ISSN: 1588-2837
    Keywords: Non-stationary kinetics ; alkylbenzene ; oxidation ; oxide catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A non-stationary kinetic model for deep oxidation of aromatic hydrocarbons based on the fragmentation theory approach is proposed. The model is simple and provides qualitative adequacy and good quantitative description of experimental results.
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    Reaction kinetics and catalysis letters 68 (1999), S. 237-242 
    ISSN: 1588-2837
    Keywords: Diols ; oxidation ; ozone ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of the oxidation of diols by ozone was investigated by a spectrophotometric method in the temperature interval of 277–304 K. The activation parameters of the reaction were determined.
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    Reaction kinetics and catalysis letters 68 (1999), S. 257-263 
    ISSN: 1588-2837
    Keywords: Alphatic alcohols ; oxidation ; ozone ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of oxidation of aliphatic alcohols by ozone in aqueous solutions was investigated in the temperature interval of 292–317 K. The activation parameters of the reaction were determined. The dissociation energies of CH-bonds of the studied substrates were calculated with the use of the AM1 semiempirical method.
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  • 66
    ISSN: 1588-2837
    Keywords: Heteropoly acids ; dialkylquinones ; preparation ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new method is proposed for synthesis of 2,6-dialkyl-1,4-benzoquinones by oxidation of 2,6-dimethyl and 2,6-di-tert-butylphenols with oxygen in a two-phase “water-organic” system in the presence of P−Mo−V heteropoly acids.
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  • 67
    ISSN: 1588-2837
    Keywords: Mechanism ; oxidation ; methyl phenyl sulfide ; hydrogen peroxide ; titanium-substituted heteropolytungstates ; peroxo complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Acid tetrabutylammonium salts of Ti(IV)-monosubstituted heteropolytungstate, PW11TiO40 5−, show high catalytic acitivity in the oxidation of methyl phenyl sulfide with hydrogen peroxide, while the corresponding tetrabutylammonium salts containing no protons are poor catalysts for this reaction.
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  • 68
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    Reaction kinetics and catalysis letters 66 (1999), S. 245-249 
    ISSN: 1588-2837
    Keywords: Montmorillonite clay ; peroxodiphosphate ; oxidation ; benzylic alcohols
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Clay-supported potassium peroxodiphosphate efficiently oxidizes benzylic alcohols to the corresponding aldehydes without overoxidation to acids. H3P2Og − as the active species.
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  • 69
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    Reaction kinetics and catalysis letters 67 (1999), S. 83-88 
    ISSN: 1588-2837
    Keywords: Manganese/ruthenium catalysts ; oxidation ; alkanes ; tert-butyl hydroperoxide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Di- and trinuclear clusters of manganese and ruthenium were used as catalysts in the oxidation of alkanes in the presence oftert-butyl hydroperoxide as oxidant. The investigations reveal marked differences in the reactivity of the manganese and ruthenium catalysts though structurally they have similar coordination environment. The probable mechanism of hydroxylation in these systems is discussed.
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    Reaction kinetics and catalysis letters 67 (1999), S. 359-364 
    ISSN: 1588-2837
    Keywords: Mechanism ; oxidation ; alkylperoxo complexes of titanium(IV) ; 13C NMR spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Using13C and1H NMR spectroscopy, titanium(IV) alkylperoxo complexes Ti(OOtBu)n(OiPr)4−n with n=1, 2, 3 and 4 were characterized in the reaction of Ti(OiPr)4 withtBuOOH in CH2Cl2 and CDCl3.
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  • 71
    ISSN: 1573-904X
    Keywords: oxidation ; antioxidants ; stability testing ; lovastatin ; simvastatin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of oxidation of the HMG-CoA reductase inhibitors lovastatin, simvastatin, L-157,012, and L-647,318 were studied in an aqueous surfactant solution. A thermally labile free radical initiator was used to attain measurable reaction rates at 40°C and rate constants were determined by measuring oxygen consumption using an oxygen electrode. The stability of the drugs was found to increase in the order lovastatin = simvastatin 〈 L-157,012 〈 L-647,318. The addition of butylated hydroxyanisole (BHA) was found to stabilize the drugs. For the oxidation of lovastatin, the effectiveness of antioxidants increased in the order propyl gallate 〈 BHA 〈 alpha-tocopherol. It is concluded that the stability of oxidizable drugs can be rapidly and conveniently assessed by the techniques described herein.
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    International journal of peptide research and therapeutics 6 (1999), S. 359-369 
    ISSN: 1573-3904
    Keywords: chemotaxis ; inflammation ; oxidation ; post-translational ; S100
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The functional importance of members of the S100 Ca2+-binding protein family is recently emerging. A variety of activities, several of whcih are apparently opposing, are attributed to S100A8, a protein implicated in embryogenesis, growth, differentiation, and immune and inflammatory processes. Murine (m) S100A8 was initially described as a chemoattractant (CP-10) for myeloid cells. It is coordinately expressed with mS100A9 (MRP14) in neutrophils and the non-covalent heterodimer is presumed to be the functional intracellular species. The extracellular chemotactic activity of mS100A8, however, is not dependent on mS100A9 and occurs at concentrations (10−13-10−11 M) at which the non-covalent heterodimer would probably dissociate. This review focuses on the structure and post-translational modifications of mS100A8/A9 and their effects on function, particularly chemotaxis.
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    International journal of peptide research and therapeutics 6 (1999), S. 359-369 
    ISSN: 1573-3904
    Keywords: chemotaxis ; inflammation ; oxidation ; post-translational ; S100
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The functional importance of members of the S100 Ca2+-binding protein family is recently emerging. A variety of activities, several of which are apparently opposing, are attributed to S100A8, a protein implicated in embryogenesis, growth, differentiation, and immune and inflammatory processes. Murine (m) S100A8 was initially described as a chemoattractant (CP-10) for myeloid cells. It is coordinately expressed with mS100A9 (MRP14) in neutrophils and the non-covalent heterodimer is presumed to be the functional intracellular species. The extracellular chemotactic activity of mS100A8, however, is not dependent on mS100A9 and occurs at concentrations (10-13–10-11 M) at which the non-covalent heterodimer would probably dissociate. This review focuses on the structure and post-translational modifications of mS100A8/A9 and their effects on function, particularly chemotaxis.
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