Mechanism of enhanced oxidation ability of dilute nitric acid and dissolution of pure gold in seawater with nitric acid

M. Hojo
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引用次数: 1

Abstract

It has been discovered that dilute nitric acid in reversed micelle systems can oxidize the Br- ion to Br2 and we have proposed that the nitryl (or nitronium) ion NO2+ should be the active species in the oxidation process. Nitration of phenol in reversed micelle systems with dilute nitric acid, CHCl3/CTAC/H2O (2.0 mol dm-3 HNO3 in the 1.0% (v/v) H2O phase), has been performed at 35 oC to obtain 2- and 4-nitrophenols, where CTAC represents cetyltrimethylammonium chloride. In aqueous 2.0 mol dm-3 HNO3 solution accompanied by 4.0 mol dm-3 LiCl (and a small amount of LiBr as the bromide resource), trans-1,4-dibromo-2-butene was successfully brominated to 1,2,3,4-tetrabromobutane. This result is good evidence that the Br- ion can be oxidized to Br2 in dilute nitric acid (2.0 mol dm-3) providing it contains concentrated salts. For chloride salts, the cation effects increased as Et4N+ << Na+ < Li+ < Ca2+ < Mg2+. Even the evolution of Cl2 has been demonstrated from < 2.0 mol dm-3 HNO3 solution containing concentrated LiCl, MgCl2, and CaCl2 as well as AlCl3. The dissolution of precious metals (Au, Pt, and Pd), especially, of gold has been demonstrated in 0.1 - 2 mol dm-3 HNO3 accompanied by alkali metal, alkaline earth metal, and aluminum chlorides. The complete dissolution time of pure gold plate (20±2 mg, 0.1 mm thickness) in 2.0 mol dm-3 HNO3 accompanied by 1.0 mol dm-3 AlCl3 has been shortened remarkably with temperature increase from 15 to 80 oC. The dissolution rate constants, log (k /s-1), of a piece of gold wire (19.7±0.5 mg) in 20 mL of 2.0 mol dm-3 HNO3 accompanied by the metal chlorides, in general, increase with increasing salt concentrations at 40 and 60 oC. The gold can be dissolved in the solution of <1.0 mol dm-3 HNO3 and <1.0 mol dm-3 HCl, i.e. a “dilute aqua regia." We have achieved a total dissolution of five pieces of the gold wire (totally 0.10 g) in 100 mL of the 1:1 mixture between seawater and 2.0 mol dm-3 HNO3 at ca. 100 oC.
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硝酸增强稀硝酸氧化能力及溶解纯金的机理
研究发现,稀硝酸在反胶束体系中可以将Br-离子氧化为Br2,并提出硝基离子NO2+应是氧化过程中的活性物种。苯酚在含有稀硝酸CHCl3/CTAC/H2O(在1.0%(v/v)H2O相中为2.0 mol dm-3 HNO3)的反胶束体系中的硝化反应已在35℃下进行,以获得2-和4-硝基苯酚,其中CTAC表示十六烷基三甲基氯化铵。在2.0mol dm-3 HNO3水溶液中,伴随着4.0mol dm-3 LiCl(和少量LiBr作为溴化物资源),反式-1,4-二溴-2-丁烯成功地溴化为1,2,3,4-四溴丁烷。这一结果很好地证明了Br-离子可以在稀硝酸(2.0mol dm-3)中氧化为Br2,只要它含有浓盐。对于氯化物盐,阳离子效应随着Et4N+<
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