利用自行研制的激光悬浮区熔设备制备了Al2O3/YAG/ZrO2 三元过共晶自生复合材料. 在过共晶成分下获得了不含初生相的全共晶层片状组织.详细分析了固/液界面形貌形成原因, 并由界面形貌出发阐述了Al2O3/YAG/ZrO2 三元过共晶组织织构化趋势.结果表明, 低凝固速率下, 三元过共晶成分下层片间距大于三元共晶成分下层片间距,而在高凝固速率下则相反, 这主要是由于ZrO2的加入影响了体系的传热及传质条件, 通过经典非规则共晶模型综合分析了传输条件对层片间距的影响.过共晶平均层片间距(λav)与凝固速率(V)满足λavV0.5=14.7 μm1.5s-0.5,符合JH模型. 对于激光加工中经常出现的带状组织形成机理也进行了讨论.
Due to the excellent high temperature mechanical properties, Al2O3/YAG/ZrO2 ternary eutectic in situ composite is considered to be a promising candidate for the material, replacement for nickel based superalloy, of new generation aero space engine turbine blade. The directionally solidified Al2O3/YAG/ZrO2 hypereutectic ceramics are prepared with recently developed laser floating zone melting (LFZM) apparatus. Full eutectic lamellar microstructure, free of primary phase, was obtained with hypereutectic composition. The formation of solid/liquid interface morphology was analyzed in detail. The microstructure texture tendency was explained by combination with interface morphology. The experimental result indicates that, just as the prediction of JH model, average spacing of hypereutectic (λav) agrees with the inverse–square–root dependence on solidification rate (V ) according to λavV 0.5=14.7 μm1.5·s−0.5. In lower solidification rate, the lamellar spacing of hypereutectic is higher than that of eutectic composition, but the situation reverses in higher rate. The main reason of such phenomenon is that the addition of ZrO2 effects the thermal and solute transformation in the melt. The influence of transformation condition on lamellar spacing was analyzed synthetically by using classical irregular growth model. The formation mechanism of banded microstructure, often observed in laser zone melted solidification processing, was also discussed.
[1] Waku Y, Nakagawa N, Wakamoto T, Ohtsubo H, Shimizu K, Kohtoku Y. Nature, 1997; 389: 49
[2] Waku Y, Nakagawa N, Wakamoto T, Ohtsubo H, Shimizu K, Kohtoku Y. J Mater Sci, 1998: 1217
[3] Su H J, Zhang J, Liu L, Fu H Z. Acta Metall Sin, 2008; 44: 457
(苏海军, 张军, 刘林, 傅恒志. 金属学报, 2008; 44: 457)
[4] Su H J, Zhang J, Cui C J, Liu L, Fu H Z. Mater Sci Eng, 2008; A479: 380
[5] Fritsch M, Klemm H. J Eur Ceram Soc, 2008; 28: 2353
[6] Fritsch M, Klemm H, Herrmann M, Schenk B. J Eur Ceram Soc, 2006; 26: 3557
[7] Ochiai S, Ueda T, Sato K, Hojo M, Waku Y, Nakagawa N, Sakata S, Mitani A, Takahashi T. Compos Sci Technol, 2001; 61: 2117
[8] Lee J H, Yoshikawa A, Kaiden H, Lebbou K, Fukuda T, Yoon D H, Waku Y. J Cryst Growth, 2001; 231: 179
[9] Larrea A, Orera V M, Merino R I, Pe˜na J I. J Eur Ceram Soc, 2005; 25: 1419
[10] Oliete P B, Pe˜na J I, Larrea A, Orera V M, Llorca J, Pastor J Y, Mart´?n A, Segurado J. Adv Mater, 2007; 19: 2313
[11] Calderon–Moreno J M, Yoshimura M. J Eur Ceram Soc, 2005; 25: 1365
[12] Pe˜na J I, Larsson M, Merino R I, Francisco I D, Orera V M, Llorca J, Pastor J Y, Mart´?n A, Segurado J. J Eur Ceram Soc, 2006; 26: 3113
[13] Su H J, Zhang J, Cui C J, Liu L, Fu H Z. J Cryst Growth, 2007; 307: 448
[14] Ester F J, Larrea A, Merino R I. J Eur Ceram Soc, 2011; 31: 1257
[15] Kurz W, Fisher D J. Int Met Rev, 1979; (5–6): 177
[16] Lakiza S M, Lopato L M. J Am Ceram Soc, 1997; 80: 893
[17] Echigoya J, Takabayashi Y, Sasaki K. Trans Jpn Inst Met, 1986; 27: 102
[18] Jackson K A, Hunt J D. Aime Met Soc Trans, 1966; 236: 1129
[19] Llorca J, Orera V M. Prog Mater Sci, 2006; 51: 711
[20] Flood S C, Hunt J D. J Mater Sci, 1981; 15: 287
[21] Merino R I, Pe N A J I, Larrea A, de la Fuente G F, Orera V M. Recent Res Devel Mater Sci, 2003; 4: 1
[22] Golubovi´c A, Nikoli´c S, Gaji´c R, Duri´c S, Valˇci´c A. J Serb Chem Soc, 2005; 70: 87
[23] Calderon–Moreno J M, Yoshimura M. Mater Sci Eng, 2004; A375–377: 1250
[24] Magnin P, Kurz W. Acta Metall, 1987; 35: 1119
[25] Liu L, Huang T, Qu M, Liu G, Zhang J, Fu H. J Mater Process Technol, 2010; 210: 159
[26] Oliete P B, Pe˜na J I. J Cryst Growth, 2007; 304: 514
[27] Sola D, Ester F J, Oliete P B, Pe˜na J I. J Eur Ceram Soc, 2011; 31: 1211
[28] Saitou M. J Appl Phys, 1997; 12: 6343
[29] Uhlmann D R, Chalmers B, Jackson K A. J Appl Phys, 1964; 10: 2986
[30] Winegard W C, Majka S, Thall B M, Chalmers B. Can J Chem, 1951; 29: 320