一种基于铂和铑的推力合金的开启强化

A. V. Egoshina, G. B. Slepchenko
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摘要

基于铂族金属的合金中固有的高耐化学性是溶解此类材料时出现许多困难的原因之一。王水溶出法是目前溶解耐蚀合金最有效的方法之一。这种方法的主要缺点是释放有毒气体物质,如亚硝基氯和氮氧化物。为了在不降低系统氧化还原电位的情况下减少释放气体的体积,我们提出了一种将Pt - Rh合金溶解在HCl-HNO3中,并在给定系统氧化还原电位(ORP)值下控制剂量的hno3供应的方法。从hno3 - HCl- Pt和hno3 - HCl- rh体系的电位出发,选择了该体系的电位,分别为0.85 V和0.9 V。同时考虑了PtRh合金的弥散和固有缺陷对合金溶出指标的影响。结果表明,Pt - Rh的解散与铑合金含量15%的盐酸- HNO 3 ORP的恒定值= 0.9 V相比,使用经典的混合物(HCl: HNO 3 = 1:3卷。)提供了一个硝酸消耗减少40%,减少过程的时间,提高采收率的铂和铑,公布的的体积和减轻了1/2氮氧化物(理论计算)。合金的机械活化过程缩短了试样的溶解时间,使试样几乎定量溶解。
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Intensification of opening a thrust alloy based on platinum and rhodium
A high chemical resistance inherent in the alloys based on platinum group metals is one of the reasons for a number of difficulties that arise when dissolving such materials. Nowadays, the dissolution in aqua regia is one of the most effective methods for dissolving corrosion-resistant alloys. The main disadvantage of this method is a release of toxic gaseous substances such as nitrosyl chloride and nitrogen oxides. To decrease the volume of gases thus released without reducing the redox potential of the system, we proposed a method of dissolving a Pt – Rh alloy in HCl-HNO3 with a controlled dosed supply of HNO 3 at a given value of the oxidation-reduction potential (ORP) of the system. The potential of the system has been chosen proceeding from the potential for HNO 3 – HCl – Pt and HNO 3 – HCl-Rh systems and amounted to 0.85 and 0.9 V. The impact of the dispersion and the inherent flaw of PtRh alloys on the dissolution indices of the alloy was also considered. It is shown that the dissolution of a Pt – Rh alloy with a rhodium content of 15 % in HCl – HNO 3 at a constant value of ORP = 0.9 V compared to the use of the classic mixture (HCl:HNO 3 = 1:3 vol.) provides a decrease in nitric acid consumption by 40%, reduction of the process time, increase in the recovery factor for both platinum and rhodium, and a two-fold reduction of the volume of released nitrogen oxides (theoretical calculation). It is also revealed that the process of mechanical activation of the alloy reduces the dissolution time and leads to almost quantitative dissolution of the sample.
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