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Reinvestigation of the kinetics of reduction of bromite by hexacyanoferrate(II) in slightly basic solution

机译:再研究在弱碱性溶液中六氰合铁酸盐(II)还原溴铁矿的动力学

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摘要

The reaction BrO_2~- + 4Fe(CB)_6~(4-) + 2H_2O → Br~- + 4 Fe(CN)_6~(3-) + 4OH~- has been studied by spectrophotometry at 30, 40 and 50 ℃ and both with equivalent amounts of reactants and with an excess of bromite. It follows the kinetic expression (dξ)/(dt) = k_(obs) [BrO_2~-][Fe(CN)_6~(4-)]~2 with k_(obs) = 8.2 M~(-2) s~(-1) at 25 ℃, ΔH~≠ = 66 kJ mol~(-1) and ΔS = -121.7 J K~(-1) mol~(-1). The proposed mechanism is a two-stage process, the first, rate-determining stage being reduction of bromite to hypobromous acid, the second further reduction to bromide. Either stage consists of two bimolecular reactions. The major contribution to the energy barriers comes from electrostatic repulsion between negative ions.
机译:通过分光光度法在30、40和50℃下研究了BrO_2〜-+ 4Fe(CB)_6〜(4-)+ 2H_2O→Br〜-+ 4 Fe(CN)_6〜(3-)+ 4OH〜-的反应以及等量的反应物和过量的溴石矿。它遵循动力学表达式(dξ)/(dt)= k_(obs)[BrO_2〜-] [Fe(CN)_6〜(4-)]〜2,其中k_(obs)= 8.2 M〜(-2)s 〜(-1)在25℃时,ΔH〜≠= 66 kJ mol〜(-1),ΔS= -121.7 JK〜(-1)mol〜(-1)。所提出的机理是一个两阶段的过程,第一个决定速率的阶段是将溴酸盐还原为次溴酸,第二个进一步还原为溴化物。任一阶段均由两个双分子反应组成。对能垒的主要贡献来自负离子之间的静电排斥。

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