High temperature corrosion behavior and mechanism of steel slag-based glass ceramic in the eutectic carbonates

IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS
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Abstract

Steel slag-based glass ceramic for thermal energy storage was first fabricated by quenching method, and then their high temperature corrosion behavior in the eutectic carbonates and related mechanism have been investigated using X-ray diffraction,Raman spectroscopy and scanning electron microscope techniques. The results show that holding time has a significant influence on the corrosion layer thickness at 800oC. As the holding time was extended, the thickness of the corrosion layer with obvious cracks tended to increase. Further EDS analyses disclosed that the divided corrosive layers along the extended directions of the cracks should be similar in both the compositions and microstructure. Based on these observations, the possible corrosion mechanism was discussed after defining phase structure of nonstoichiometric (Fe0.35Al0.20Mg0.44) Ca0.96(Fe0.08Si0.70Al0.20)2O6.12 as a combined system of CaMgSi2O6(Di)-CaFe3+AlSiO6(Es)-CaAl2Si2O8(An). Oxygen offered by the molten carbonates salt is regarded to play a critical role in the corrosion process. In an atmosphere rich in oxygen, both Na+ and K+ ions diffused into the diopside can replace Ca2+ and Mg2+, etc. resulting in polyhedral structural reorganization for electrical neutrality. On the other hand, the bonding stability of the cation-oxygen bonds in diopside was proved to be weaker than that in single oxides. These two aspects contribute to the continuous dissolution of Ca2+ and Mg2+, etc. in the molten carbonates salt.

钢渣基玻璃陶瓷在共晶碳酸盐中的高温腐蚀行为和机理
首先采用淬火方法制备了用于热能储存的钢渣基玻璃陶瓷,然后利用 X 射线衍射、拉曼光谱和扫描电子显微镜技术研究了其在共晶碳酸盐中的高温腐蚀行为及相关机理。结果表明,保温时间对 800oC 时的腐蚀层厚度有显著影响。随着保温时间的延长,带有明显裂纹的腐蚀层厚度有增加的趋势。进一步的 EDS 分析表明,沿着裂纹延伸方向划分的腐蚀层在成分和微观结构上应该是相似的。根据上述观察结果,在确定了非全度(Fe0.35Al0.20Mg0.44)Ca0.96(Fe0.08Si0.70Al0.20)2O6.12 相结构为 CaMgSi2O6(Di)-CaFe3+AlSiO6(Es)-CaAl2Si2O8(An) 组合体系后,讨论了可能的腐蚀机制。熔融碳酸盐提供的氧气被认为在腐蚀过程中起着至关重要的作用。在富含氧气的环境中,扩散到透辉石中的 Na+ 和 K+ 离子可以取代 Ca2+ 和 Mg2+ 等离子,从而导致多面体结构重组,实现电中性。另一方面,透辉石中阳离子-氧键的成键稳定性比单一氧化物弱。这两个方面导致 Ca2+ 和 Mg2+ 等在熔融碳酸盐盐中不断溶解。
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来源期刊
Ceramics International
Ceramics International 工程技术-材料科学:硅酸盐
CiteScore
9.40
自引率
15.40%
发文量
4558
审稿时长
25 days
期刊介绍: Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties. Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour. Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.
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