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  • 1
    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.
    Type of Medium: Electronic Resource
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  • 2
    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.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1588-2837
    Keywords: AlPO4 ; CrPO4 ; CrPO4−AlPO4 ; surface acidity ; 3,3-dimethyl-1-butene isomerization ; poisoning by bases ; pyridine ; 2,6-dimethylpyridine ; hexamethyldisilazane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The skeletal isomerization of 3,3-dimethyl-1-butene over AlPO4 (Al/P=1), CrPO4 (Cr/P=1), and CrPO4−AlPO4 (CrAlP, 5–10 wt.% AlPO4) catalysts is a first order reaction. Catalytic performance is affected by the precipitation agent. CrPO4 catalysts obtained in propylene oxide-aqueous ammonia showed the highest activity. Moreover, the incorporation of AlPO4 to CrPO4 developed CrAlP catalysts that exhibited increased activity, irrespective of the precipitation method, as compared with both AlPO4 and CrPO4 catalysts. Besides, CrAlP catalysts prepared in propylene oxide-aqueous ammonia were the more active ones.
    Type of Medium: Electronic Resource
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