Felix-Contreras Rafael, de la Vega Olivas Jonathan, Arrieta-Gonzalez Cinthya Dinorah, Chacon-Nava Jose Guadalupe, Rodriguez-Diaz Roberto Ademar, Gonzalez-Rodriguez Jose Gonzalo, Porcayo-Calderon Jesus
Departamento de Ingenieria Quimica y Metalurgia, Universidad de Sonora, Hermosillo 83000, Sonora, Mexico.
Tecnológico Nacional de Mexico/Instituto Tecnológico de Zacatepec, Calzada Instituto Tecnológico 27, Zacatepec 62780, Morelos, Mexico.
Materials (Basel). 2024 Nov 25;17(23):5776. doi: 10.3390/ma17235776.
The study and improvement of the corrosion resistance of materials used in concentrated solar power plants is a permanent field of research. This involves determining their chemical stability when in contact with heat transfer fluids, such as molten nitrate salts. Various studies indicate an improvement in the corrosion resistance of iron-based alloys with the incorporation of elements that show high reactivity and solubility in molten nitrate salts, such as Cr and Mo. This study analyzes the kinetic and thermodynamic aspects of the beginning of the corrosion process of ferritic steels immersed in Solar Salt at 400, 500, and 600 °C. The analysis of the kinetic data using the Arrhenius equation and the Transition State Theory shows that an increase in the Cr/Mo ratio reduces the activation energy, the standard formation enthalpy, and the standard formation entropy. This indicates that its incorporation favors the degradation of steel; however, the results show a reduction in the corrosion rate. This effect is possible due to a synergistic effect by the formation of insoluble Fe-oxide layers that favor the formation of a Cr oxide layer at the Fe-oxide-metal interface, which limits the subsequent oxidation of Fe.
聚光太阳能发电厂所用材料的耐腐蚀性研究与改进是一个长期的研究领域。这涉及确定材料在与传热流体(如熔融硝酸盐)接触时的化学稳定性。各种研究表明,通过加入在熔融硝酸盐中显示出高反应性和溶解性的元素(如Cr和Mo),铁基合金的耐腐蚀性有所提高。本研究分析了铁素体钢在400、500和600℃的太阳能盐中浸泡时腐蚀过程开始的动力学和热力学方面。使用阿累尼乌斯方程和过渡态理论对动力学数据进行分析表明,Cr/Mo比的增加降低了活化能、标准生成焓和标准生成熵。这表明其加入有利于钢的降解;然而,结果显示腐蚀速率降低。这种效应可能是由于形成了不溶性铁氧化物层的协同效应,该层有利于在铁氧化物-金属界面形成Cr氧化物层,从而限制了Fe的后续氧化。