Preparation, characterization and surface acid catalytic activity of microporous clays pillared with Al1-xFexOy (x=0.00 to 1.00) oxidic species

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Stathopoulos, V. N.
Ladavos, A. K.
Kolonia, K. M.
Skaribas, S. P.
Petrakis, D. E.
Pomonis, P. J.

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Elsevier

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peer reviewed

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Microporous and Mesoporous Materials

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Montmorillonite was pillared with mixed oxidic species of the form Al1-xFexOy where x = 0.00, 0.05, 0.15, 0.25, 0.50, 0.75 and 100. The pillaring agent was an alkaline solution of the corresponding quantities of metal nitrates so as to obtain a final ratio (Al + Fe)/OH = 1:2. The specific surface area (BET) of the samples dried at 500 degrees C was found to be 230 +/- 10 m(2) g(-1) for x = 0.00 - 0.50 and similar to 139 +/- 8 m(2) g(-1) for x = 0.75-1.00. The XRD results obtained at low angles from samples oriented along the (001) axis showed gallery heights of the heated solids of 16-17 Angstrom for x = 0.00 - 0.50 and 9.9 - 9.8 Angstrom for x = 0.75 - 1.00. The acidity of the samples, checked by TPD of NH3, varied from similar to 12 x 10(17) sites m(-2) (x greater than or equal to 0.25) to similar to 9 x 10(17) sites m(-2) (x less than or equal to 0.75). The acid catalytic activity of the solids was checked using the isopropanol (IPA) decomposition as a probe reaction. The main products observed were propene (selectivity greater than or equal to 80%) and di-iso-propyl ether (DIPE) (selectivity less than or equal to 20%). The apparent activation energies for the TPA conversion were calculated, and the selectivity dependence on temperature was kinetically modelled. From this, a mechanism was derived to account for the reactions of one or two IPA molecules towards propene or DIPE, respectively, and the dependence of the selectivity on the Al/Fe ratio and the acidity of the solids. (C) 1999 Elsevier Science B.V. All rights reserved.

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acid catalysis, acidity, clays, microporous, pillared, montmorillonite, smectites, complexes

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<Go to ISI>://000082838400010
http://ac.els-cdn.com/S138718119900061X/1-s2.0-S138718119900061X-main.pdf?_tid=0477f165fd0514ee0bb7ca141a6b98e7&acdnat=1333035680_9cd23dc2bce74bbc434374513f1a0ba0

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en

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Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας

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