TY - JOUR
T1 - A Comparative Study of Cyclic Oxidation and Sulfates-Induced Hot Corrosion Behavior of Arc-Sprayed Ni-Cr-Ti Coatings at Moderate Temperatures
AU - Guo, Wenmin
AU - Wu, Yuping
AU - Zhang, Jianfeng
AU - Hong, Sheng
AU - Chen, Liyan
AU - Qin, Yujiao
N1 - Funding Information:
The authors appreciate the financial supports from Fundamental Research Funds for the Central Universities (2013B34414, 2013B22814), National Natural Science Foundation of China (50979028), Natural Key Foundation of Jiangsu Provience (BK2011025) and National 973 Plan Project (2015CB057803).
Publisher Copyright:
© 2015, ASM International.
PY - 2015/6/28
Y1 - 2015/6/28
N2 - The cyclic oxidation and sulfates-induced hot corrosion behaviors of a Ni-43Cr-0.3Ti arc-sprayed coating at 550-750 °C were characterized and compared in this study. In general, all the oxidation and hot corrosion kinetic curves of the coating followed a parabolic law, i.e., the weight of the specimens showed a rapid growth initially and then reached the gradual state. However, the initial stage of the hot corrosion process was approximately two times longer than that of the oxidation process, indicating a longer preparation time required for the formation of a protective scale in the former process. At 650 °C, the parabolic rate constant for the hot corrosion was 7.2 × 10−12 g2/(cm4·s), approximately 1.7 times higher than that for the oxidation at the same temperature. The lower parabolic rate constant for the oxidation was mainly attributed to the formation of a protective oxide scale on the surface of corroded specimens, which was composed of a mixture of NiO, Cr2O3, and NiCr2O4. However, as the liquid molten salts emerged during the hot corrosion, these protective oxides would be dissolved and the coating was corrupted acceleratedly.
AB - The cyclic oxidation and sulfates-induced hot corrosion behaviors of a Ni-43Cr-0.3Ti arc-sprayed coating at 550-750 °C were characterized and compared in this study. In general, all the oxidation and hot corrosion kinetic curves of the coating followed a parabolic law, i.e., the weight of the specimens showed a rapid growth initially and then reached the gradual state. However, the initial stage of the hot corrosion process was approximately two times longer than that of the oxidation process, indicating a longer preparation time required for the formation of a protective scale in the former process. At 650 °C, the parabolic rate constant for the hot corrosion was 7.2 × 10−12 g2/(cm4·s), approximately 1.7 times higher than that for the oxidation at the same temperature. The lower parabolic rate constant for the oxidation was mainly attributed to the formation of a protective oxide scale on the surface of corroded specimens, which was composed of a mixture of NiO, Cr2O3, and NiCr2O4. However, as the liquid molten salts emerged during the hot corrosion, these protective oxides would be dissolved and the coating was corrupted acceleratedly.
KW - arc spray
KW - coating
KW - hot corrosion
KW - oxidation
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U2 - 10.1007/s11666-015-0222-6
DO - 10.1007/s11666-015-0222-6
M3 - Article
AN - SCOPUS:84929956358
SN - 1059-9630
VL - 24
SP - 789
EP - 797
JO - Journal of Thermal Spray Technology
JF - Journal of Thermal Spray Technology
IS - 5
ER -