Abstract
The regularities of ethoxylation of benzoic acid derivatives during interaction with polyethylene glycol through mechanochemical solid-phase synthesis in a vibrating apparatus have been studied. The conditions for carrying out mechanochemical reactions to increase the conversion degree of initial reagents into reaction products are analysed. The products of ethoxylation are characterized by IR spectroscopy, acid-base potentiometric titration, tensiometry, and dilatational rheology. It has been established that the degree of starting reagents conversion into ethoxylation products depends on the nature of the substituent and its position in the benzene ring. The degree of conversion into reaction products is higher for ortho-substituted derivatives of benzoic acid. It is shown that the salts of ethoxylated derivatives of benzoic acid exhibit pronounced surfactant properties at the air - solution interface.
Published Version
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