کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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149598 | 456434 | 2012 | 10 صفحه PDF | دانلود رایگان |
Detailed thermodynamic and kinetic study of the aqueous Kolbe–Schmitt synthesis of beta-resorcylic acid has been carried out in a laboratory-scale batch reactor operated under ambient pressure. The dependence of the conversion on partial pressure of carbon dioxide (4 × 10−4 − 1 bar), initial concentration of resorcinol (0.4–0.8 M), initial concentration of potassium bicarbonate (0.4–6 M) and temperature (348–428 K) was studied. The reaction was found to be reversible and exothermic (ΔH = −30.4 kJ/mol). Partial pressure of carbon dioxide does not influence the reaction kinetics when carried out in the excess of potassium bicarbonate (CKHCO3,0/CR,0 > 1). Increase of the initial concentration of potassium bicarbonate accelerates drastically the rate and shifts the equilibrium conversion to higher values. For the first time a reliable kinetic model has been proposed based on two reversible reactions of pseudo first order towards resorcinol and beta-resorcylic acid. The kinetic constants showed Arrhenius dependencies on the reaction temperature with the apparent energies of activation 105 and 125 kJ/mol for the forward and the reversed reactions, respectively. Pre-exponential factors increased with the initial concentration of potassium bicarbonate indicating a complexity of the reaction mechanism involved. The kinetic model was successfully validated against experimental data obtained under high pressure and temperature using a micro-plant. Finally, the model was found consistent with the literature data available for this reaction.
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► Kinetics and thermodynamics of the aqueous Kolbe–Schmitt synthesis were studied.
► The reaction was found to be reversible and exothermic (ΔH = −30.4 kJ/mol).
► A kinetic model has been proposed consistent with experimental and literature data.
Journal: Chemical Engineering Journal - Volumes 200–202, 15 August 2012, Pages 738–747