CATALITIC INFLUENCE OF COBALT (II) ON THE KINETICS OF CUMENE HYDROPEROXIDE METHIONINE REACTION IN AQUEOUS SOLUTIONS
DOI:
https://doi.org/10.46991/PYSU:B/2008.42.3.112Keywords:
cumene hydroperoxide, cobalt, IR spectroscopy, kinetic lawAbstract
The complexformation of methionine (Met) with cobalt ion in aqueous solutions has been investigated by IR spectroscopy and kinetic methods. It has been shown that two types: 1:1 and 2:1 complexes are formed between the ligande and metal ion. In the system 1:1 complex predominates, which have catalytic activity on the cumene hydroperoxide (CHP) decomposition in aqueous solutions, where a reaction between Met and CHP takes place. The kinetic law of hydroperoxide (ROOH) catalytic decomposition at the presence of [CoMet]2+ complex is found: W0 = –d[ROOH]/dt = Kcat[Co2+]0[Met][ROOH]0 = Keff[ROOH]0. Temperature dependence of Keff is expressed by the following equation: Keff = (1.12 ± 0.05)105exp[(–43000 ± 300)/RT], min–1.
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