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Acetic acid was supplied by Sigma and ethanol and ethyl acetate were supplied by Merck. The components were degassed ultrasonically,dried over molecular sieves (type4A,Aldrich),and kept in an inert argon with a maximum water content  of 2*10-6mass fraction. Their mass fraction purities were>99 mass% for acetic acid and>99.8 mass% for methanol,ethanol and ethyl acetate. The water was bidistillated and deionized.
    The catalyst used was an ion-exchange resin Amberlyst 15 supplied by Supelco.The catalyst was washed with ethanol and water to remove impurities and dried at 363.15K. Mean diameter of the resin beads,obtained by scanning electron microscopy, is 7.6*10-3m.
   A Hewlett-Packard 6890GC chromatograph was used to determine the composition of the samples.The gas chromatograph column was HP-FFAP polyethylene glycol TPA equipped with series of connected thermal conductivity and  flame ionization detectors to detect water and the other compounds in the same run.Helium was used as carrier at a flow rate of 6.8 *10-8m-3 s-1 . Injector, detectors and oven temperature were 473.15,503.15 and 423.15K,respectively.To know the composition of these quaternary mixtures it is necessary to have
quaternary patrons of known composition,so 249 quaternary mixtures were prepared by mass and were measured by gas chromatography.
     The experiments were performed in a stirred glass reactor with a volume of 1.5*10-4m 3. The temperature in the reactor was maintained within+0.1K. The acetic acid and the catalyst were heated at reaction temperature,ethanol was heated separately.When temperature reaction is reached,the second reactant  was added to the mixture in the reactor and this was considered  the starting time of the reaction.During each experiment, samples of about 5*10-7m3  were taken and cooled to avoid vaporization before analyzing.
     The homogeneous reactions, esterification or hydrolysis,are catalyzed by the acetic acid.Table1 summarizes the experiments made at 303.15, 323.15 and 353.15K. The duration of each experiment to reach chemical equilibrium is indicated in the third column.

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Acetic acid was supplied by Sigma and ethanol and ethyl acetate were supplied by Merck. The components were degassed ultrasonically,dried over molecular sieves (type4A,Aldrich),and kept in an inert argon with a maximum water content  of 2*10-6mass fraction. Their mass fraction purities were>99 mass% for acetic acid and>99.8 mass% for methanol,ethanol and ethyl acetate. The water was bidistillated and deionized.
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