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1100 ℃水氧环境下Mini-SiCf/BN/SiC的基体/界面/纤维一体化氧化机制

戚芳1, 刘辉1, 吴郑敏1, 陆毅1, 吴雯雯2, 王震1   

  1. 1.乌镇实验室,桐乡 314000;
    2.陕西师范大学 物理学与信息技术学院,西安 710000
  • 收稿日期:2025-06-12 修回日期:2025-08-08
  • 作者简介:戚芳(1996-), 女, 硕士研究生. E-mail: qif@wuzhenlab.com
  • 基金资助:
    国家重点研发计划 (2022YFB3707700)

Matrix/Interface/Fiber Integrated Oxidation Mechanism of Mini-SiCf/BN/SiC under Water Oxygen Environment at 1100℃

QI Fang1, LIU Hui1, WU Zhengmin1, LU Yi1, WU Wenwen2, WANG Zhen1   

  1. 1. Wuzhen Laboratory, Tongxiang 314000, China;
    2. School of Physics and Information Technology, Shaanxi Normal University, Xi'an 710000, China
  • Received:2025-06-12 Revised:2025-08-08
  • About author:QI Fang (1996–), female, Master candidate. E-mail: qif@wuzhenlab.com
  • Supported by:
    National Key R&D Program of China (2022YFB3707700)

摘要: SiCf/SiC复合材料具备耐高温、抗氧化、高强度等特性,在航空航天热防护领域具有重要应用前景。在服役条件下,材料需长期承受热、水、氧等多种环境因素的耦合作用,其失效机理和损伤规律极为复杂。本研究以SiCf/BN/SiC迷你复合材料(Mini-SiCf/BN/SiC)为试材,通过多尺度宏观/微观表征手段,探究其在1100 ℃水氧耦合环境下的循环氧化行为,重点分析基体/界面/纤维一体化氧化机制。结果表明:氧化初期,试材表面的基体在生成无定型SiO2玻璃层,表面相对光滑;随着氧化过程的持续,SiO2结晶度逐渐提高,导致氧化层局部剥落,表面粗糙度(Sa)先减小后增大。XRM分析结果表明,经循环氧化处理后,试材内部产生大量微小缺陷,缺陷数目呈数量级增加(约107倍),小尺寸缺陷主要分布于基体表面,且氧化产物对缺陷起到一定填充作用。试材拉伸性能在循环氧化前后未发生显著变化,分别为(328.47±32.84) MPa和(343.27±35.71) MPa,这表明“强基体-弱界面”的协同氧化增韧机制仍有效。具体而言,平行于纤维轴方向,界面层和附近基体、纤维生成的SiO2和硼硅酸盐玻璃能够填充缺陷;垂直于纤维轴方向,基体内形成的动态“外层多孔可牺牲层-中层致密SiO2-内层SiC基体”三维防护屏障,构成了基体/界面/纤维一体化氧化机制,可显著缓解热-水-氧环境下循环氧化对材料的侵蚀。

关键词: Mini-SiCf/BN/SiC, 循环氧化, 高温水氧环境, 多尺度表征, 氧化机制

Abstract: SiCf/SiC composites exhibit advantages such as high temperature resistance, oxidation resistance, and high strength, making them a "star" candidate material in the field of aerospace thermal protection. Under operational conditions, these materials are subjected to prolonged multiple coupled fields such as heat, water, and oxygen, exhibiting complex failure mechanisms and damage evolution patterns. This study investigated the integrated oxidation mechanism of the matrix/interface/fiber in Mini-SiCf/BN/SiC composites under cyclic oxidation at 1100 ℃ in a water-oxygen coupled environment, by using multi-scale macro/micro characterization techniques. The results showed that during the initial oxidation stage, an amorphous SiO2 glass layer with relatively smooth morphology formed on the material surface. However, with the increase in crystallinity, localized spallation occurred in the oxide layer, causing the surface roughness (Sa) to initially decrease before subsequently increasing. XRM results showed that numerous micro-defects were generated within the material after cyclic oxidation, and the number of defects increased by orders of magnitude (about 107 fold). The majority of these micro-defects were mainly distributed on the matrix surface, and the oxidation products played a certain filling role in these defects. The tensile strength showed no significant variation before ((328.47±32.84) MPa) and after ((343.27±35.71) MPa) cyclic oxidation, indicating the continued effectiveness of the synergistic toughening mechanism of "strong matrix-weak interface". These observations indicate that an integrated oxidation protection mechanism involving the matrix, interface, and fiber is established. This mechanism is predicated on the filling of defects by SiO2 and borosilicate glass generated by the interface layer and adjacent matrix and fibers in the direction parallel to the fiber axis, and the dynamic "outer porous sacrificial layer-middle dense SiO2-inner SiC matrix" three-dimensional protective barrier of the matrix in the direction perpendicular to the fiber axis. This dual-protection system substantially alleviates material degradation under cyclic thermal water oxidative conditions.

Key words: Mini-SiCf/BN/SiC, cyclic oxidation, high temperature water oxygen environment, multi-scale representation, integrated oxidation mechanism

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