Kinetics and Mechanism of Chromium(III) Catalysed Oxidation of Propan-1-ol and Butan-1-ol by Cerium(IV) in Aqueous Sulfuric acid Media

A. Das, S. Mondal, D. Kar, M. Das
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引用次数: 2

Abstract

The kinetics and mechanism of chromium(III) catalysed oxidation of propan-1-ol and butan-1-ol by cerium(IV) in aqueous sulfuric acid media have been studied at different temperatures (30-40° C) under the conditions, [substrate]T(0.025-0.70 mol dm-3) × [CeIV]T (2.5-4.5 × 10-3 mol dm-3) in the presence of [Cr]T = 0.0025-0.07 mol dm-3. At fixed [H+] and [HSO-4 ] the observed rate law conforms to: -d ln[CeIV]/df =kobs =A[S]T[Cr]T/{B + C[Cr]T(D + E[S]T)}, where, A, B, C, D and Ε are constants expressed in terms of different rate constants and equilibrium constants; [S]Tand [Cr]T denote the total substrate (i.e. propan-l-ol or butan-l-ol) and total chromium concentration respectively. The proposed mechanism involves the association of catalyst, substrate and oxidant at some pre-equilibrium steps before the electron transfer step. The overall process is found catalysed by H+ . From the [HSO-4] dependence, Ce(SO4)2 has been found kinetically active.
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硫酸水溶液中铬(III)催化铈(IV)氧化丙-1-醇和丁-1-醇的动力学及机理
在[Cr]T = 0.0025-0.07 mol dm-3的条件下,[底物]T(0.025-0.70 mol dm-3) × [CeIV]T (2.5-4.5 × 10-3 mol dm-3),在不同温度(30-40℃)条件下,研究了铬(III)在硫酸水溶液中催化铈(IV)氧化丙烯-1-醇和丁烷-1-醇的动力学和机理。在固定的[H+]和[HSO-4]下,观察到的速率定律符合:-d ln[CeIV]/df =kobs =A[S]T[Cr]T/{B + C[Cr]T(D + E[S]T)},其中A、B、C、D和Ε是用不同的速率常数和平衡常数表示的常数;[S]和[Cr]T分别表示总底物(即丙醇或丁醇)和总铬浓度。所提出的机理涉及催化剂、底物和氧化剂在电子转移步骤之前的一些预平衡步骤中的结合。整个过程是由H+催化的。从[HSO-4]依赖性来看,Ce(SO4)2具有动力学活性。
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