A novel effective hydration of carbon monoxide in liquid phase by a water-soluble ruthenium complex catalyst at moderate pressures in aqueous medium

• Published in: Applied catalysis. A, General General, 2005-10, Vol.294 (1), p.111-118
• Main Authors: Shukla, Ram S., Bhatt, Sharad D., Thorat, Ravikumar B., Jasra, Raksh V.
• Format: Article
• Language: English
• Subjects: Carbon monoxide; Catalysis; Chemistry; Exact sciences and technology; Formic acid; General and physical chemistry; Hydration; Kinetics; Mechanism; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Thermodynamics
• ISSN: 0926-860X; 1873-3875
• DOI: 10.1016/j.apcata.2005.07.034

A ruthenium-based complex, ethylenediaminetetraacetato ruthenate [Ru-EDTA(H 2O)] − 1 was found to be an efficient homogeneous catalyst to activate carbon monoxide as well as water molecule in hydration of CO. It was investigated at moderate pressures (5–20 atm) and at 10–40 °C for direct conversion of CO to formic acid (FA). In typical catalytic experiments conducted in a pressure reactor of 300 ml capacity, 75 × 10 −3 M of FA was found to be formed at 10 atm CO pressure and 40 °C. The kinetics of the (i) complexation of CO with 1 and (ii) hydration of CO to formic acid reactions were investigated in detail by studying the rate of formation of intermediate Ru-EDTA-CO complex 2 and the rate of formation of FA, respectively as a function of the concentration of the catalyst 1, CO pressure, reaction temperature, ionic strength and pH. The rate of formation of FA was found to be first order with respect to the concentration of 1 and CO pressure, independent of pH and ionic strength, and dependent on temperature, in agreement with the Arrhenius equation. Similar kinetic profile and temperature dependence were observed for formation of complex 2 also. Activation parameters evaluated from temperature dependence were found to be favorable for the formation of 2 and the CO hydration product FA. Based on kinetic and experimental results, a mechanism for the hydration of CO to formic acid is suggested.