Tuesday, 4 October 2016

Kinetics and Mechanism of Ethyl Acetate Production Using Eco-Benign Solid Catalyst


Esterification reaction generally refers to the formation of esters by the interaction of alcohols and carboxylic acids. Alternatively, it refers to as the process of formation of an ester by the reaction between an alkanol and an acid. It is a reversible process and does not proceed to any appreciable extent in the absence of catalysts or supercritical condition. This process is described as an acidcatalyzed equilibrium synthesis developed by Emil Fischer. It is the simplest pathway among several pathways used in synthesis of esters. When catalysed by a strong acid usuallytetraoxosulphate (VI) acid, the reaction is called Fisher esterification. This important process is one of the most organic reactions in chemical and allied industries visa vis its applications as intermediate in the synthesis of fine chemicals, drugs, perfumes, food preservatives, and also in the production of biodiesels via transesterification. It is widely applied from the preparation of highly specialized esters in the chemical laboratory to the production of millions of tons of commercial ester products. 

Kinetics and Mechanism of Ethyl Acetate Esterification process can be carried out either as a batch or a continuous process. The batch procedure involves a single pot reactor that is filled with the acid and alcohol reactants. The acid catalyst is added and the water removed as the reactionproceeds. This method is most often used in the chemical laboratories, but in a few cases, it is used by industry to make large quantities of esters. Ethyl acetate is a colorless liquid with a characteristic smell.

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