Development of high stability catalysts to facilitate CO2 capture into water - an alternative to monoethanolamine and amine solvents

The aim is to develop a catalysed water-based capture process, avoiding the energy intensive steam stripping steps necessary with amine solvents. The naturally occurring zinc metallo-enzyme carbonic anhydrase/hydratase (CAH) can concentrate CO2 using a reversible hydration/dehydration cycle at neutral pH and at ambient temperatures. Some tripodal complexes of zinc (II)-[zinc-itrilo-tris(2-benzimidazoyl-methyl-6-sulfonic acid, (zinc-L1S), and zinc-tris(2-benzimidazoylmethyl)-amine, (zinc-LI)], and also cadmium (II), cobalt (II) and other metals complexed to these tripodal ligands have been prepared, and show activity that mimics the CAH catalytic process-hydration of CO2 to bicarbonate followed by the reverse dehydration of the bicarbonate to regenerate CO2 in a pH dependent mechanism. The thermal stability of these complex catalysts has been demonstrated by Differential Thermo-Gravimetric (DTG) studies to above 200 °C. A process for fast absorption/desorption is proposed.