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  • 1
    ISSN: 1572-879X
    Keywords: alcohols ; ethers ; SN2 mechanism ; MTBE ; ETBE
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Reaction of CH3 18OH with16O-containing isobutanol (2-methylpropan-1-ol) over strong acid Nafion-H and Amberlyst-H 35 resin catalysts gave the two distinctly labelled C5 ethers 1-methoxy(16O)-2-methylpropane (also designated as methyl isobutyl ether,16O-MIBE) and 2-methoxy(18O)-2-methylpropane (also designated as methyl tertiary-butyl ether,18O-MTBE). Reaction of CH3CH2 18OH with isobutanol gave the analogously labelled C6 ethers,16O-EIBE and18O-ETBE. These results show that the isobutyl and tertiary-butyl ethers are formed from the alcohols by distinctly different mechanistic pathways, i.e. the former are produced bysurface-catalyzed SN2 reactions that follow Langmuir-Hinshelwood kinetics involving competitive adsorption while the latter arise via carbenium or olefinic intermediates. There is no pathway for isomerization of the two ethers, MIBE and MTBE, under the reaction conditions employed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 11-12 (2000), S. 111-122 
    ISSN: 1572-9028
    Keywords: selective catalytic reduction ; V2O5–WO3/TiO2 catalysts ; V2O5–MoO3/TiO2 catalysts, DeNOx-SCR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A comparison between commercial and model WO3–V2O5/TiO2 and MoO3–V2O5/TiO2 SCR catalysts is considered in this study. The data indicate that WO3 and MoO3 behave as “structural” and “chemical” promoters for the catalysts. MoO3-based catalysts are more active but less selective than WO3–V2O5/TiO2 catalysts in the SCR reaction, although in the presence of water the catalytic performances of the investigated samples are comparable.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 41 (1996), S. 35-39 
    ISSN: 1572-879X
    Keywords: NOx reduction ; selective catalytic reduction ; V2O5-WO3/TiO2 catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reactivity of ternary V2O5-WO3/TiO2 De-NO x catalysts is investigated by transient and steady-state techniques, and results have been compared with those obtained over binary V2O5/TIO2 samples having the same V2O5 loading. The results indicate that the reactivity of the ternary catalysts in the SCR reaction is higher than that of the vanadia-titania samples, and that at low temperatures the SCR reaction occurs via a redox mechanism that involves at first the participation of the catalyst lattice oxygen and then the reoxidation of the reduced sites by gas-phase oxygen. Accordingly, the higher reactivity of the ternary catalysts has been related to their superior redox properties.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-879X
    Keywords: methane coupling ; lanthanum titanate catalysts ; OCM
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reactivity of lanthanum titanate catalysts is investigated in the oxidative coupling of methane (OCM) under lean-oxygen conditions. The catalyst performances are influenced by the catalyst preparation method and by the amounts of the alkali dopant. A transient method was also used to study the mobility of lattice oxygen species under OCM reaction conditions. It is found that (i) in the absence of gas phase oxygen the sample does not possess lattice oxygen species which participate in the reaction; (ii) the alkali doping does not appreciably modify the mobility of lattice oxygen; and (iii) the role of the alkali promoter in the reaction is that of modifying the surface acid/base and oxidizing properties.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-879X
    Keywords: catalytic combustion ; biogas ; ammonia oxidation ; Mn‐substituted hexaaluminate catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reactivity of a Mn‐substituted hexaaluminate catalyst in the catalytic combustion of gasified biomasses‐derived fuels is addressed. The combustion activity of the main fuel components, i.e., CO, H2, C2H4 and CH4, is investigated, along with that of NH3 that is present in the biomasses‐derived fuels. It is found that significant amounts of NOx are formed from ammonia during the catalytic combustion process, but the occurrence of gas‐phase homogeneous reactions involving NH3 and NO in the presence of oxygen strongly reduce NOx formation at high temperatures.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 43 (1997), S. 2559-2570 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The unsteady-state kinetics of NH3 adsorption-desorption and of selective catalytic reduction (SCR) of NO with NH3 were studied over model V2O5/TiO2 and V2O5-WO3/TiO2 catalysts by transient response techniques. Over both catalysts the dynamic experiments could be successfully described by a kinetic model assuming (1) negligible NO adsorption on the catalyst surface; (2) nonactivated NH3 adsorption; (3) a Temkin-type NH3 coverage dependence of the desorption energy; (4) a nonlinear dependence of the SCR reaction rate on the NH3 surface coverage. Thus, the results are supportive of an Eley-Rideal mechanism for the SCR reaction and of a significant heterogeneity for adsorption-desorption process and surface reaction of the catalyst surface. The binary and ternary catalysts exhibit similar acid properties, but different activity in the SCR reaction, possibly related to the superior redox properties of the WO3-containing sample. Over both samples the estimates of the activity energies for NH3 desorption at zero coverage and for the surface reaction of NO with NH3 are similar and in the 23-26 and 14-16 kcal/mol ranges, respectively.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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