Process Safety and Environment Protection Research Group, School of Engineering, The University of Newcastle, Callaghan, New South Wales 2308, Australia.
Inorg Chem. 2012 Feb 20;51(4):2178-85. doi: 10.1021/ic202081z. Epub 2012 Feb 3.
Decomposition of nitrous acid in aqueous solution has been studied by stopped flow spectrophotometry to resolve discrepancies in literature values for the rate constants of the decomposition reactions. Under the conditions employed, the rate-limiting reaction step comprises the hydrolysis of NO(2). A simplified rate law based on the known elementary reaction mechanism provides an excellent fit to the experimental data. The rate constant, 1.34 × 10(-6) M(-1) s(-1), is thought to be of higher accuracy than those in the literature as it does not depend on the rate of parallel reaction pathways or on the rate of interphase mass transfer of gaseous reaction products. The activation energy for the simplified rate law was established to be 107 kJ mol(-1). Quantum chemistry calculations indicate that the majority of the large activation energy results from the endothermic nature of the equilibrium 2HNO(2) ⇆ NO + NO(2) + H(2)O. The rate constant for the reaction between nitrate ions and nitrous acid, which inhibits HNO(2) decomposition, was also determined.
通过停流分光光度法研究了亚硝酸在水溶液中的分解,以解决文献中关于分解反应速率常数的差异。在采用的条件下,限速反应步骤包括 NO(2)的水解。基于已知的基本反应机制的简化速率定律与实验数据非常吻合。该速率常数 1.34×10(-6) M(-1) s(-1) 被认为比文献中的速率常数更准确,因为它不依赖于平行反应途径的速率或气相反应产物的相间传质速率。简化速率定律的活化能被确定为 107 kJ mol(-1)。量子化学计算表明,大部分大的活化能是由于平衡 2HNO(2) ⇆ NO + NO(2) + H(2)O 的吸热性质所致。还确定了抑制 HNO(2)分解的硝酸盐离子与亚硝酸之间的反应速率常数。