MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young...MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young’s modulus.The underlying linkage between the structural evolution and the crystallization characteristics of the MCAS system was systematically investigated using molecular dynamics simulation and thermodynamic calculation.The results revealed that Mg^(2+) ions played a dual role,constructing networks through the formation of tricluster oxygens while consuming bridging oxygens(BOs)in a mechanism similar to Ca^(2+) ions.However,despite this dual role,the network connectivity was still decreased with the increase in MgO/(MgO+Al_(2)O_(3))(M/(M+A))and CaO/(CaO+SiO_(2))(C/(C+S))ratios,primarily due to the reduction in BOs.This microscopic structural evolution resulted in a reduction in viscosity and an enhancement of crystallization ability.Furthermore,the remarkable diffusion capability of Mg^(2+) ions,coupled with the increased proportion of 6-coordinated Mg^(2+)ions,unveiled the mechanism underlying the precipitation of MgSiO_(3) and Mg_(2)SiO_(4) crystals,which exhibited high Young’s moduli of 165.23 and 196.67 GPa,respectively.To prevent the precipitation of MgO-rich crystalline phases,it was crucial to maintain the M/(M+A)ratio below 0.42 and the C/(C+S)ratio below 0.16 within the MCAS system.展开更多
为研究真空等离子喷涂Si/Yb_(2)Si_(2)O_(7)/Yb_(2)SiO_(5)环境障涂层试样在涂层受压、涂层受拉时的室温弯曲强度及失效原因,采用超景深三维显微镜、SEM(Scanning Electron Microscope)等方法对喷涂后的试样进行了表征,并测量了涂层孔隙...为研究真空等离子喷涂Si/Yb_(2)Si_(2)O_(7)/Yb_(2)SiO_(5)环境障涂层试样在涂层受压、涂层受拉时的室温弯曲强度及失效原因,采用超景深三维显微镜、SEM(Scanning Electron Microscope)等方法对喷涂后的试样进行了表征,并测量了涂层孔隙率;采用拉伸法测试了涂层的结合强度,并采用三点弯曲试验测试了裸材、涂层受压和涂层受拉时的室温弯曲强度。结果表明:Si/Yb_(2)Si_(2)O_(7)/Yb_(2)SiO_(5)涂层与SiC_(f)/SiC复合材料的结合强度为10.13 MPa,拉伸断裂主要在复材表层发生。计算涂层厚度时,涂层受压样的弯曲强度(503.21 MPa)与裸材(506.79 MPa)基本一致;不计算涂层厚度时,涂层受拉样的弯曲强度(499.77 MPa)与裸材一致;EBC涂层整体具有一定的压缩强度,其整体抗拉强度比复材自身抗拉强度小很多。压涂层时,在载荷增加至接近最大载荷时,复材层间发生破坏,并逐步失效,随后涂层发生飞崩,载荷迅速下降,试验停止;拉涂层时,在载荷很小时(约64 N)涂层就被拉开,随着载荷增加,直至接近最大载荷时,层间发生破坏并逐步失效。弯曲试验时复材的主要失效模式是SiC纤维断裂、复材的SiC基体开裂和复材层间撕裂,复材受拉面产生复材厚度方向的纵向裂纹;复材表层沉积的SiC膜层失效模式主要是开裂和剥落;EBC涂层在受压时的主要失效模式是整体飞崩和开裂,在受拉时,涂层在最大应力处断裂为2部分。本研究对含EBC涂层的SiC_(f)/SiC复材的最大弯曲载荷设计具有参考意义.展开更多
基金support from the National Key R&D Program of China(Grant Nos.2023YFB3709900 and 2023YFB3709903)the National Natural Science Foundation of China(Grant Nos.52174293 and U22A20171)+1 种基金the High Steel Center(HSC)at North China University of TechnologyUniversity of Science and Technology Beijing(USTB).
文摘MgO has been shown to facilitate the precipitation of MgO-rich crystalline phases within the MgO-CaO-Al_(2)O_(3)-SiO_(2)(MCAS)glassy inclusion system,which possesses a high liquidus temperature and a significant Young’s modulus.The underlying linkage between the structural evolution and the crystallization characteristics of the MCAS system was systematically investigated using molecular dynamics simulation and thermodynamic calculation.The results revealed that Mg^(2+) ions played a dual role,constructing networks through the formation of tricluster oxygens while consuming bridging oxygens(BOs)in a mechanism similar to Ca^(2+) ions.However,despite this dual role,the network connectivity was still decreased with the increase in MgO/(MgO+Al_(2)O_(3))(M/(M+A))and CaO/(CaO+SiO_(2))(C/(C+S))ratios,primarily due to the reduction in BOs.This microscopic structural evolution resulted in a reduction in viscosity and an enhancement of crystallization ability.Furthermore,the remarkable diffusion capability of Mg^(2+) ions,coupled with the increased proportion of 6-coordinated Mg^(2+)ions,unveiled the mechanism underlying the precipitation of MgSiO_(3) and Mg_(2)SiO_(4) crystals,which exhibited high Young’s moduli of 165.23 and 196.67 GPa,respectively.To prevent the precipitation of MgO-rich crystalline phases,it was crucial to maintain the M/(M+A)ratio below 0.42 and the C/(C+S)ratio below 0.16 within the MCAS system.
