TY - JOUR
T1 - On the reactive spark plasma sinterability of ZrB2–SiC–TiN composite
AU - Ahmadi, Zohre
AU - Shahedi Asl, Mehdi
AU - Zakeri, Mohammad
AU - Farvizi, Mohammad
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/7/15
Y1 - 2022/7/15
N2 - In the present research, the influence of TiN addition on the ZrB2–SiC composite was studied. Hereof, TiN-doped ZrB2–SiC composite was manufactured via the route of reactive spark plasma sintering under an applied load of 40 MPa at the peak temperature of 1850 °C for 360 s. Mechanical properties, microstructure evaluation, and sinterability were investigated and compared to the non-doped ZrB2–SiC. X-ray diffraction analysis, thermodynamic appraisal, energy dispersive spectroscopy, and scanning electron microscopy divulged the formation of in-situ h-BN, ZrO2, and ZrN as well as the (Zr,Ti)B2 solid solution in TiN-doped ZrB2–SiC. Comparing the relative density of 95% for the TiN-free sample with the relative density of 94.1% for the sample containing TiN, the addition of TiN increased porosity content owing to the formation of in-situ BN with layered structure. Flexural strength decreased from 460.2 MPa for TiN-free ZrB2–SiC to 435.9 MPa for TiN-doped ZrB2–SiC, due to matrix grain growth and relative density drop. In contrast, indentation fracture toughness and Vickers hardness increased to 6.1 MPa.m1/2 and 29.1 GPa, respectively, as the result of TiN addition.
AB - In the present research, the influence of TiN addition on the ZrB2–SiC composite was studied. Hereof, TiN-doped ZrB2–SiC composite was manufactured via the route of reactive spark plasma sintering under an applied load of 40 MPa at the peak temperature of 1850 °C for 360 s. Mechanical properties, microstructure evaluation, and sinterability were investigated and compared to the non-doped ZrB2–SiC. X-ray diffraction analysis, thermodynamic appraisal, energy dispersive spectroscopy, and scanning electron microscopy divulged the formation of in-situ h-BN, ZrO2, and ZrN as well as the (Zr,Ti)B2 solid solution in TiN-doped ZrB2–SiC. Comparing the relative density of 95% for the TiN-free sample with the relative density of 94.1% for the sample containing TiN, the addition of TiN increased porosity content owing to the formation of in-situ BN with layered structure. Flexural strength decreased from 460.2 MPa for TiN-free ZrB2–SiC to 435.9 MPa for TiN-doped ZrB2–SiC, due to matrix grain growth and relative density drop. In contrast, indentation fracture toughness and Vickers hardness increased to 6.1 MPa.m1/2 and 29.1 GPa, respectively, as the result of TiN addition.
KW - Mechanical properties
KW - Microstructure
KW - Reactive spark plasma sintering
KW - UHTCs
UR - http://www.scopus.com/inward/record.url?scp=85127359515&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2022.164611
DO - 10.1016/j.jallcom.2022.164611
M3 - Article
AN - SCOPUS:85127359515
SN - 0925-8388
VL - 909
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
M1 - 164611
ER -