I. Introduction
Thermochromic (TC) materials respond to changes of temperature by colour change [1]. Organic thermochromic material has become a hot topic because of its low toxicity, high sensitive and functional, especially for the compounds contained with Schiff base structure. Schiff bases in a broad sense have the general formula , where R is an organic side chain. On the Natural Hybrid Orbital, there is lone pair electrons from N atom which endowed it with important implications of biological and chemical. At present, its application domain involves topharmacy [2], catalysis [3], analytical chemistry [4], and corrosion [5] and so on. Along with the unceasing development of Schiff base material, the compounds with adjacent hydroxyl has been studied comprehensively. For example, someone has reported that the thermochromism of salicylideneanilines [6], salicylidene benzylamines [7], and 1-(Naphthalen-l-yliminomethyl)-naphthalen-2-o1 [8]. However, all of those are solid crystalline polymer, salicylaldehayde-ethanolamine Schiff base is liquid and water solubility. According to the literature, the relatively well known medical functionality of salicylaldehayde-ethanolamine [9], very little has been published about its colorimetric characteristics. This paper concerns the kinetic study and thermochromism properties of salicylaldehayde-ethanolamine Schiff base condensation reaction. Special attention was devoted to the thermochromism properties that describe colour hysteresis and the influence of temperatures in excess of the activation temperature on the reversibility of the thermochromic process.