欢迎登录材料期刊网

材料期刊网

高级检索

用低压化学气相沉积(LPCVD)法,以丙烯(C_3H_6)为碳源,氮气(N_2)为稀释气制备了2.5维连续碳化硅纤维增韧碳化硅(SiC_f/SiC)复合材料的碳界面层,其厚度为~0.1 mm.研究了不同丙烯含量(体积分数,下同)(60%,50%,45%)对碳层形貌、微观结构及SiC_f/SiC力学性能的影响.结果表明:当C_3H_6含量为60%时,热解碳层表面光滑,石磨化度高;当C_3H_6为50%和45%时,碳层粗糙,有很多较大颗粒存在,石磨化度低.3种复合材料的弯曲强度差别不大,分别为303,311和320 MPa.然而,当C_3H_6含量为60%时,材料韧性断裂,断裂功高;为50%和45%时,材料脆性断裂,断裂功低.不同的纤维拔出滑移阻力是SiC_f/SiC断裂行为不同的原因.

Pyrocarbon interlayer of 2.5-dimension silicon carbide fiber reinforced silicon carbide composites was prepared by low pressure chemical vapor deposition (LPCVD) method using propylene as carbon source and nitrogen as diluent gas. The thickness of the interlayer is about 0.1mm. The effects of propylene content (60%, 50%, 45%) on the morphology, microstructure of the carbon coating and the mechanical properties of the composites were studied. The carbon coating has smooth surface, high graphitization degree when the propylene content is 60%; rough surface, low graphitization degree when the content is 50% and 45%. There is little difference between the flexural strength (303, 311 and 320 MPa) of the composites. However composite has a high work of fracture and fractures in a non-catastrophic mode when propylene content is 60%; a low work of fracture and fractures in a catastrophic mode when the content is 50% and 45%. Different interfacial sliding resistances is the reason for the different fracture behaviors of the composites.

参考文献

[1] Carrere N;Martin E;Lamon J .[J].Compos A,2000,31(11):1179.
[2] Jose Perez-Rigueiro;Jose Antonio Celemin;Javier LLorca;Pilar Herrero .Oxidation of BN/Nicalon fiber interfaces in ceramic-matrix composites and its effect on fiber strength[J].Journal of the American Ceramic Society,1999(12):3494-3500.
[3] Miller JH.;Landes JD.;Liaw PK. .Influence of fiber coating thickness on fracture behavior of continuous woven Nicalon((R)) fabric-reinforced silicon-carbide matrix ceramic composites[J].Materials Science & Engineering, A. Structural Materials: Properties, Misrostructure and Processing,2001(1-2 Special Issue SI):49-58.
[4] Kazuya Shimoda;Joon-Soo Park;Tatsuya Hinoki .[J].Composites Science and Technology,2008,28(01):98.
[5] Jean-Marie V;Xavier B;Arnaud M et al.[J].Carbon,2006,44:1833.
[6] 张福勤,黄启忠,黄伯云,巩前明,陈腾飞,熊翔.C/C复合材料石墨化度的喇曼光谱表征[J].无机材料学报,2003(02):361-366.
[7] Williama C .[J].Journal of the American Ceramic Society,1991,74(11):2837.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%