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  • MgO  (2)
  • 2-chilorophenol  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 51 (1998), S. 183-185 
    ISSN: 1572-879X
    Schlagwort(e): CH4 ; CO2 ; Ni ; MgO ; lattice oxygen ; transient response
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The CO2 reforming of methane over reduced NiO/MgO solid solution catalysts was studied at 800°C by a novel transient method, which couples a broadened pulse of CH4/CO2 with a step change to the carrier gas and/or with a sharp isotopic pulse of either 18O4, CO18 2 or 13CO16 2. The response curves indicated that two kinds of oxygen were formed over the catalysts during reaction: adsorbed oxygen which reacts fast with C species and lattice oxygen which reacts more slowly with C species. One concludes that a redox cycle of lattice oxygen formation through the oxidation of Ni and its reaction with C species takes place on the catalyst surface.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 57 (1999), S. 167-169 
    ISSN: 1572-879X
    Schlagwort(e): CD4 ; CH4 ; GC-MS ; lattice oxygen ; NiO ; MgO ; solid solution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The reaction between methane and the lattice oxygen of a NiO/MgO (1/1.85) solid solution was investigated by an isotopic pulse-GCMS method. During a single-pulse reaction of CH4/CD4 (1/1) with the lattice oxygen, besides CH4, CD4, carbon monoxide and water, very small amounts of CHD3, CH2D2 and CH3D were detected in the exit gas. Because the isotopic kinetic effect (KH/KD) was 1.01, the dissociation of CH4 cannot constitute the rate-determining step. The rate-determining step is the reaction with the lattice oxygen, because of the high stability of the lattice oxygen in the NiO/MgO solid solutions.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 44 (1994), S. 79-86 
    ISSN: 0006-3592
    Schlagwort(e): lignin peroxidase ; Phanerochaete chrysosporium ; white-rot-fungus ; polymers ; immobilization ; 2-chilorophenol ; biodegradation ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: Porous poly(styrene-divinylbenzene) carriers, for the immobilization of white rot fungus Phanerochaete chrysosporium have been prepared by the concentrated emulsion polymerization method. The concentrated emulsion consists of a mixture of styrene and divinylbenzene containing a suitable surfactant and an initiator as the continuous phase, and water as the dispersed phase. The polymerization of the monomers of the continuous phase generated the polymer carrier with a porcus structure. The white rot fungus Phanerochaete chrysosporium has been immobilized on porous poly(styrene-divinylbenzene) carriers and used for the batch production and the repeated batch production of lignin peroxidase in shake cultures based on a carbon-limited medium containing veratryl alcohol. The best results were achieved when a spore inoculum was used for immobilization instead of 1-day-old mycelial pellets, for both the batch production and the repeated batch production. The porous poly(styrene-divinylbenzene) immobilized Phanerochaete chrysosporium and freely suspended mycelial pellets were used as biocatalysts for the degradation of 2-chilorophenol in a 2-L bioreactor. The porous poly(styrene-divinylbenzene) particle (diameter ≅ 0.2 cm) immobilized spores exhibited a much higher activity in the degradation of 2-chlorophenol than the freely suspended mycelial pellets. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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