Zeolite catalysts as solid solvents in fine chemicals synthesis - 2. Competitive adsorption of the reactants and products in the Friedel-Crafts acetylations of anisole and toluene
Eg. Derouane et al., Zeolite catalysts as solid solvents in fine chemicals synthesis - 2. Competitive adsorption of the reactants and products in the Friedel-Crafts acetylations of anisole and toluene, J CATALYSIS, 194(2), 2000, pp. 410-423
The liquid-phase acetylations of anisole by acetic anhydride and isopropeny
l acetate and that of toluene by acetic anhydride, using zeolites HBEA, HMF
I, and HFAU as catalysts, were carried out under batch conditions using var
ious molar ratios of the reactants without added solvent. Evidence has been
obtained for competitive adsorption effects of the reactants resulting fro
m differences in their adsorption equilibrium constants (AEC). Estimated va
lues of the AEC show that preferential adsorption is in the order toluene <
acetic anhydride (AA) < anisole < isopropenyl acetate (IPA). In all cases,
the acetylation products are adsorbed more strongly than the reactants, bu
t the competitive adsorption of acetic acid and acetone appear to be neglig
ible when AA and IPA are used as acetylating agents, respectively. The effe
ct of dealumination was investigated for the acetylation of toluene by acet
ic anhydride, using HBEA as catalyst. Both the initial and the quasistation
ary-state reaction rates are proportional to Al content, i.e., the number o
f Bronsted sites at low Al content. The rates decrease at high aluminium co
ntent, indicating that competitive adsorption effects are enhanced due to t
he increased zeolite polarity and polarisability. Initial rate constants fo
r the acetylation of anisole, derived by assuming a Langmuir-Hinshelwood mo
del, show that the rate-determining step is most likely to be the reaction
of anisole with an acyl cation equivalent formed by reaction of either acet
ic anhydride or isopropenyl acetate with the zeolite (HBEA). A possible mec
hanism is proposed in which the formation of an acyl cation-zeolite complex
is the initial step. This proposal is based in part on the colour change o
f the zeolite when it is contacted with the reactant mixture and during rea
ction, the colour being attributed to the formation of the zeolite-acyl cat
ion complex. The present work confirms that competitive adsorption effects,
involving both reactants and products, need to be controlled in order to a
chieve maximum catalytic performance when zeolites are used as catalysts in
the liquid phase, (C) 2000 Academic Press.