Kinetics and Mechanism of Redox Reaction of Neutral Red with Nitrite Ion in Aqueous Acidic Medium

I. Ibrahim, S. Idris, A. D. Onu
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Abstract

The kinetics of redox reaction of neutral red, NR+, with nitrite ion, NO2-, was studied in aqueous hydrochloric acid medium under pseudo-first order conditions at 25 ± 1°C, [H+] = 2.0 × 10-3 mol dm-3, I = 0.1 mol dm-3 (NaCl) and λmax = 525 nm. The reaction was first order with respect to [NR+], [NO2-] and [H+]. The reaction displayed a negative Bronsted-Debye salt effect. There was no evidence of the formation of an intermediate complex of significant stability and free radicals are probably not present in the reaction. The observations above, coupled with the result of Michaelis-Menten plot suggests an outer sphere mechanism for the reaction. The reaction obeys the rate law: -d [NR+]/dt = (a + b [H+])[NR+][NO2-]. A plausible mechanism has been proposed for the reaction.
酸性水溶液中中性红与亚硝酸盐离子氧化还原反应动力学及机理研究
在准一级条件下,在25±1℃的盐酸水溶液中,[H+] = 2.0 × 10-3 mol dm-3, I = 0.1 mol dm-3 (NaCl), λmax = 525 nm下,研究了中性红NR+与亚硝酸盐离子NO2-的氧化还原反应动力学。[NR+]、[NO2-]和[H+]均为一级反应。反应表现出负的Bronsted-Debye盐效应。没有证据表明形成具有显著稳定性的中间复合物,自由基可能不存在于反应中。上面的观察,加上Michaelis-Menten图的结果,表明了反应的外球机制。反应遵循速率规律:-d [NR+]/dt = (a + b [H+])[NR+][NO2-]。对该反应提出了一种合理的机理。
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