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  • 1
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 52 (1987), S. 3875-3879 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 51 (1986), S. 1786-1790 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 4
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Было проведено жидкофазное восстановление различных замещенных производных нитробензолов, восстановителем служила система муравьиная кислота-триэтиламин, катализатором-Pd (0,6%) на подложке AlPO4/SiO2 (20:80 по весу). Скорость восстановления нитросоединениь, содержащих электроноакцепторный заместитель, больше, чем соответствующая скорость в случае соединений, содержащих электронодонорные заместители.
    Notes: Abstract The liquid phase reduction of different substituted nitrobenzene derivatives with the formic acid-triethylamine system has been carried out by the use of a supported palladium (0,6%) on AlPO4/SIO2 (20:80 weigth) catalyst. The reduction rate of nitrocompounds containing electron-acceptor substituents is much higher than that of electron donor-containing substrates.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 117 (1986), S. 111-121 
    ISSN: 1434-4475
    Keywords: Coumarin ; Basic catalyst ; Barium hydroxide catalyst
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Es wird die Reaktion von Diethylmalonat mit Cumarin unter der katalytischen Wirkung von aktiviertem Bariumhydroxid (C-200) in einem Fest-flüssig-System beschrieben. Es ist keineMichael-Addition zu beobachten. Es tritt eine ungewöhnliche Addition-Eliminierung an der C=O-Bindung des Cumarin ein und die dabei entstehende Verbindung wird erstmals beschrieben. Der Prozeß wird auf der Basis der mikrokristallinen Struktur des Festkörpers, der Natur der aktiven Stellen am Katalysator und der chelierenden Wirkung von Cumarin auf die Gitter-BaII-Ionen erklärt.
    Notes: Abstract The reaction of diethyl malonate and coumarin catalyzed by an activated barium hydroxide catalyst (C-200) in a solid-liquid-system is described. NoMichael addition takes place. An unusual nucleophilic addition-elimination process to the C=O bond of coumarin is observed and the new compound is described the first time. The process is explained by the microcrystalline structure of the solid, the nature of the active sites of the catalyst and the chelating action of coumarin on BaII of the lattice.
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  • 6
    ISSN: 1572-879X
    Keywords: AlPO4 ; AlPO4-Al2O3 ; surface basicity ; Langmuir adsorption ; Knoevenagel condensation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The amount of basic sites of A1PO4-Al2O3 (APA1-A, 5–15 wt% Al2O3) catalysts at two basic strengths was measured by studying the liquid-phase adsorption of two acidic molecules (benzoic acid (BA, pK = 4.2) and phenol (PH, pKa = 9.9) from cyclohexane solutions, through the application of a spectrophotometric method. The data obtained follow the Langmuir adsorption isotherm and the monolayer coverage at equilibrium (at 298 K),X m, is assumed as the amount of basic sites corresponding to the specific pK of the acid used as titrant. The amount of basic sites of any AlPO4-Al2O3 catalyst is higher than that of AlPO4, but lower than that of Al2O3. Besides, an increase in the Al2O3 content from 10 wt% gradually increases the basicity of the APA1-A catalyst. Moreover, calcination at increasing temperatures does not practically affect the surface basicity of APAl-A-5 and APAl-A-10 catalysts. However, for AlPO4 content higher than 10 wt% we observe a decrease in surface basicity, this decrease depends on alumina content, i.e. it is higher as the amount of alumina increases. The basic sites of APAl-A systems catalyze the Knoevenagel condensation ofp-methoxybenzaldehyde and malononitrile at room temperature and in the absence of solvent.
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  • 7
    ISSN: 1572-879X
    Keywords: AlPO4-Al2O3 ; fluoride ion loading ; surface acidity ; cyclohexene conversion ; cumene cracking ; poisoning by bases ; pyridine ; 2,6-dimethylpyridine ; hexamethyldisilazane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Brønsted acid sites on fluoride-modified AlPO4-Al2O3 (2.5 wt% F; APAl-P-2.5F) catalyst are poisoned by the presence of 2,6-dimethylpyridine (DMPY) and hexamethyldisilazane (HMDS), thus decreasing the catalytic activity for cyclohexene and cumene reaction processes, while the effect of pyridine (PY) was scarce. Besides, the drop in activity for cyclohexene conversion was accompanied by a change in reaction selectivity so that hydrogen transfer sites are much more sensitive to base poisoning (getting greater as the poisoning effect increased) than isomerization sites. Moreover, surface trimethylsilyl (TMS) complexes (formed by covalent reaction of HMDS with surface hydroxyls) decomposed and thus, the activity progressively increased at increasing time intervals, thus reaching greater values (at ca. 4 h) than the unpoisoned APAl-P-2.5F catalyst. So, DMPY was more suitable than PY and HMDS for the poisoning of Brønsted acid sites on APAl-P-F catalyst.
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  • 8
    ISSN: 1572-879X
    Keywords: aluminum orthophosphate (AlPO4) ; AlPO4-Al2O3 ; toluene methylation ; methanol ; activity ; selectivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Toluene methylation with methanol over AlPO4 (AP) and AlPO4-Al2O3 (APAl) catalysts, obtained through different methods, was carried out in a continuous down-flow fixed bed reactor. The main products were xylenes (XYL), although trimethylbenzenes (TMB) were also found over APAl catalysts. The benzene and ethylbenzene selectivities increased slightly with time on stream at the expense of XYL and TMB selectivities. Isomer distribution was approximately 50, 24 and 26 mol% foro-, m- andp-XYL, and 72, 27 and 0 mol% for 1,2,3-, 1,2,4- and 1,3,5-TMB. The initial reaction rate constants were higher on APA1 catalysts and, furthermore, APAl catalysts exhibited similar catalytic activities, although those obtained in ethylene or propylene oxide are the most active ones. The same occurs on AP catalysts. Moreover, the changes in catalytic activity are similar to the changes in the acidic characteristics measured, in gas phase, versus pyridine. Furthermore, the activity decreased with time on stream due to coke deposition according to the expressionk = k0 exp(-βt). The rate of deactivation, evaluated from the deactivation coefficients (β), was greater for APAl than for AP catalysts.
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  • 9
    ISSN: 1573-4803
    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 the addition of aluminium orthophosphate (Al/P=1) to sepiolite were investigated with respect to texture, porosity, surface chemistry and catalytic performance. The AlPO4-sepiolite catalysts, containing different weight compositions, were prepared by precipitation of AlPO4 (Al/P=1) with propylene oxide or aqueous ammonia on to commercial natural sepiolite. Sepiolite inhibits the AlPO4 crystallization which is found when pure AlPO4 is calcined at 873 K. The surface acid-basic properties have been studied gas-chromatographically through the irreversible adsorption of organic acids and bases at temperatures in the range 473 to 673 K. In addition, the cyclohexene skeletal isomerization (CSI) acid catalysed test reaction to 1- and 3-methylcyclopentenes (1- and 3-MCP), was used to test catalyst performance. Catalytic activity, as an apparent rate constant, fits the Bassett-Habgood kinetic model for first-order processes. Marked changes were found in their catalytic properties as a function of the preparation method and the AlPO4 to sepiolite ratio. AlPO4 addition induced acidity by increasing the strength of acid sites which resulted in a higher conversion which was accompanied by a greater selectivity for 1-MCP. The incorporation of AlPO4 to sepiolite also inhibited the loss of activity with the prolonged use of the catalyst which was found for reference pure natural sepiolite.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 31 (1986), S. 327-332 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Адсорбция серии нормальных и α-метилированных аренов на родиевых катализаторах, нанесенных на два типа AlPO4, исследована с помощью техники газо-твердой хроматографии. Процесс адсорбции экзотеричен (δHads〉0) и неспонтанен (δGads〈0). Относительные константы адсорбции подчиняются уравнению Павелича-Тафта, в котором обсловливающим влиянием является злектронный эффект алкильного заместителя.
    Notes: Abstract The adsorption of normal and α-methylated series arenes on rhodium supported on two kinds of AlPO4 has been studied by using a gas-solid chromatographic technique. The adsorption process was exothermic (δHads〈0) and non spontaneous (δGads〉0) the relative adsorption constants being fitted to the Pavelich-Taft equation in which the electrical effect of the alkyl substituent is the main influence.
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