In this work,three-dimensional(3D)Cf/SiBCN composites were fabricated by polymer infiltration and pyrolysis(PIP)with poly(methylvinyl)borosilazane as SiBCN precursor.The 3D microstructure evolution process of the comp...In this work,three-dimensional(3D)Cf/SiBCN composites were fabricated by polymer infiltration and pyrolysis(PIP)with poly(methylvinyl)borosilazane as SiBCN precursor.The 3D microstructure evolution process of the composites was investigated by an advanced X-ray computed tomography(XCT).The effect of dicumyl peroxide(DCP)initiator addition on the crosslinking process,microstructure evolution,and mechanical properties of the composites were uncovered.With the addition of a DCP initiator,the liquid precursor can cross-linking to solid-state at 120℃.Moreover,DCP addition decreases the release of small molecule gas during pyrolysis,leading to an improved ceramic yield 4.67 times higher than that without DCP addition.After 7 PIP cycles,density and open porosity of the final Cf/SiBCN composite with DCP addition are 1.73 g.cm^(-3)and〜10%,respectively,which are 143.0%higher and 30.3%lower compared with the composites without DCP addition.As a result,the flexural strength and elastic modulus of Cf/SiBCN composites with DCP addition(371 MPa and 31 GPa)are 1.74 and 1.60 times higher than that without DCP addition(213 MPa and 19.4 GPa),respectively.展开更多
Two compositions of CuPd-V system filler alloy were designed for joining the Cf/SiBCN composite. Their dynamic wettability on the Cf/SiBCN composite was studied with the sessile drop method. The CuPd-8 V alloy exhibit...Two compositions of CuPd-V system filler alloy were designed for joining the Cf/SiBCN composite. Their dynamic wettability on the Cf/SiBCN composite was studied with the sessile drop method. The CuPd-8 V alloy exhibited a contact angle of 57° after holding at 1170℃ for 30 min, whereas for CuPd-13 V alloy,a lower contact angle of 28°can be achieved after heating at 1200 ℃ for 20 min. Sound Cf/SiBCN joints were successfully produced using the latter filler alloy under the brazing condition of（1170-1230）℃for 10 min. The results showed that the active element V strongly diffused to the surface of Cf/SiBCN composite, with the formation of V2 C/VN reaction layer. The microstructure in the central part of the joint brazed at 1200 ℃ was characterized by the V2 C/VN particles distributing scatteringly in CuPd matrix. The corresponding joints showed the maximum three-point bend strength of 82.4 MPa at room temperature.When the testing temperature was increased to 600 0 C, the joint strength was even elevated to 108.8 MPa.Furthermore, the joints exhibited the strength of 92.4 MPa and 39.8 MPa at 800 ℃ and 900 ℃, respectively.展开更多
G/SiBCN ceramic composite was joined using Ni-19Cr-10Si （BNi5） and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 ℃ for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the CdSiBCN com- posi...G/SiBCN ceramic composite was joined using Ni-19Cr-10Si （BNi5） and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 ℃ for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the CdSiBCN com- posite, with a contact angle of 13° and 4°, respectively, The microstructures of the brazed joints were investigated by electron-probe microanalysis （EPMA）, and three-point bend test was conducted for the joints at room temperature. When being brazed with BNi5 filler alloy, no evident reaction layer was ob- served at the surface of the joined composite, and the joint microstructure was characterized by Ni2Si matrix with scatteringly distributing mixture compounds of Cr23C6, Ni2Si and CrB. While Ni-Cr-Pd（Si,B） brazing alloy was used, a Cr23C6 reaction layer with a thickness of 11 μm was formed at the surface of the base composite. In the central part of the brazed joint, the phases were composed of Ni（Cr, Si） solid solution and complex compounds including Pd2Si, （Ni,Pd）2Si and Ni-B. The strength of Cf/SiBCN joint brazed with BNi5 filler alloy was 62.9 MPa at room temperature, whereas that with Ni-Cr-Pd（Si,B） filler alloy was at the same level.展开更多
Using liquid poly(methylvinyl)borosilazanes(PMVBSZ)as precursor,carbon fiber reinforced SiBCN matrix composites(C_f/SiBCN)were fabricated by a modified polymer infiltration and pyrolysis(PIP)process.With dicumyl perox...Using liquid poly(methylvinyl)borosilazanes(PMVBSZ)as precursor,carbon fiber reinforced SiBCN matrix composites(C_f/SiBCN)were fabricated by a modified polymer infiltration and pyrolysis(PIP)process.With dicumyl peroxide added as cross-linking agent,the PMVBSZ could be solidified at a low temperature of 120℃,leading to a high ceramic yield of～70%.The cross-linking mechanism and ceramization processes of the precursor were investigated in detail.Moreover,a modified infiltration technology was developed,which improved the efficiency and protected the precursor against moist air during PIP.Consequently,the obtained C_f/SiBCN composites had an oxygen content of around 1.22 wt%.Benefiting from the high ceramic yield and high efficiency of the modified PIP,C_f/SiBCN composites with an open porosity of～10%and uniform microstructure were obtained after only 7 cycles of PIP.The flexural strength and fracture toughness of the derived C_f/SiBCN composites were 371 MPa and 12.9 MPa·m^(1/2),respectively.This work provides a potential route for the fabrication of high performance C_f/SiBCN composites.展开更多
基金the National Key Research and Development Program of China(2016YFB0700202)the Key Research Program of Frontier Sciences,CAS(QYZDY-SSW-JSC031)+1 种基金the National Natural Science Foundation of China(51702341,51872310)the project supported by State Key Laboratory of Advanced Technology for Materials Synthesis and Processing(Wuhan University of Technology,2021-KF-5)are greatly acknowledged.
文摘In this work,three-dimensional(3D)Cf/SiBCN composites were fabricated by polymer infiltration and pyrolysis(PIP)with poly(methylvinyl)borosilazane as SiBCN precursor.The 3D microstructure evolution process of the composites was investigated by an advanced X-ray computed tomography(XCT).The effect of dicumyl peroxide(DCP)initiator addition on the crosslinking process,microstructure evolution,and mechanical properties of the composites were uncovered.With the addition of a DCP initiator,the liquid precursor can cross-linking to solid-state at 120℃.Moreover,DCP addition decreases the release of small molecule gas during pyrolysis,leading to an improved ceramic yield 4.67 times higher than that without DCP addition.After 7 PIP cycles,density and open porosity of the final Cf/SiBCN composite with DCP addition are 1.73 g.cm^(-3)and〜10%,respectively,which are 143.0%higher and 30.3%lower compared with the composites without DCP addition.As a result,the flexural strength and elastic modulus of Cf/SiBCN composites with DCP addition(371 MPa and 31 GPa)are 1.74 and 1.60 times higher than that without DCP addition(213 MPa and 19.4 GPa),respectively.
基金financially supported by the National Natural Science Foundation of China (Grant Nos. 59905022, 50475160 and 51275497)the Aeronautical Science Foundation of China (Grant No. 2008 ZE21005)
文摘Two compositions of CuPd-V system filler alloy were designed for joining the Cf/SiBCN composite. Their dynamic wettability on the Cf/SiBCN composite was studied with the sessile drop method. The CuPd-8 V alloy exhibited a contact angle of 57° after holding at 1170℃ for 30 min, whereas for CuPd-13 V alloy,a lower contact angle of 28°can be achieved after heating at 1200 ℃ for 20 min. Sound Cf/SiBCN joints were successfully produced using the latter filler alloy under the brazing condition of（1170-1230）℃for 10 min. The results showed that the active element V strongly diffused to the surface of Cf/SiBCN composite, with the formation of V2 C/VN reaction layer. The microstructure in the central part of the joint brazed at 1200 ℃ was characterized by the V2 C/VN particles distributing scatteringly in CuPd matrix. The corresponding joints showed the maximum three-point bend strength of 82.4 MPa at room temperature.When the testing temperature was increased to 600 0 C, the joint strength was even elevated to 108.8 MPa.Furthermore, the joints exhibited the strength of 92.4 MPa and 39.8 MPa at 800 ℃ and 900 ℃, respectively.
基金financially supported by the National Natural Science Foundation of China (Contract Nos. 59905022, 50475160 and 51275497)Aeronautical Science Foundation of China (Grant 2008 ZE21005)
文摘G/SiBCN ceramic composite was joined using Ni-19Cr-10Si （BNi5） and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 ℃ for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the CdSiBCN com- posite, with a contact angle of 13° and 4°, respectively, The microstructures of the brazed joints were investigated by electron-probe microanalysis （EPMA）, and three-point bend test was conducted for the joints at room temperature. When being brazed with BNi5 filler alloy, no evident reaction layer was ob- served at the surface of the joined composite, and the joint microstructure was characterized by Ni2Si matrix with scatteringly distributing mixture compounds of Cr23C6, Ni2Si and CrB. While Ni-Cr-Pd（Si,B） brazing alloy was used, a Cr23C6 reaction layer with a thickness of 11 μm was formed at the surface of the base composite. In the central part of the brazed joint, the phases were composed of Ni（Cr, Si） solid solution and complex compounds including Pd2Si, （Ni,Pd）2Si and Ni-B. The strength of Cf/SiBCN joint brazed with BNi5 filler alloy was 62.9 MPa at room temperature, whereas that with Ni-Cr-Pd（Si,B） filler alloy was at the same level.
基金financial supports from the National Key Research and Development Program of China (No. 2017YFB0703200) National Natural Science Foundation of China (No. 51702341)Chinese Academy of Sciences Innovative Funding (No. CXJJ-17-M169)
文摘Using liquid poly(methylvinyl)borosilazanes(PMVBSZ)as precursor,carbon fiber reinforced SiBCN matrix composites(C_f/SiBCN)were fabricated by a modified polymer infiltration and pyrolysis(PIP)process.With dicumyl peroxide added as cross-linking agent,the PMVBSZ could be solidified at a low temperature of 120℃,leading to a high ceramic yield of～70%.The cross-linking mechanism and ceramization processes of the precursor were investigated in detail.Moreover,a modified infiltration technology was developed,which improved the efficiency and protected the precursor against moist air during PIP.Consequently,the obtained C_f/SiBCN composites had an oxygen content of around 1.22 wt%.Benefiting from the high ceramic yield and high efficiency of the modified PIP,C_f/SiBCN composites with an open porosity of～10%and uniform microstructure were obtained after only 7 cycles of PIP.The flexural strength and fracture toughness of the derived C_f/SiBCN composites were 371 MPa and 12.9 MPa·m^(1/2),respectively.This work provides a potential route for the fabrication of high performance C_f/SiBCN composites.
