期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 936, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.168219
关键词
High entropy alloy; Small punch testing; Finite element simulation
The suitability of determining the strain rate sensitivity (SRS) of the CoCrFeMnNi high-entropy alloy (HEA) by small punch (SP) testing has been assessed. The stress increased with the displacement rate, while the plastic strain distributions were similar. Casting defects caused a drop in strength and ductility at a higher displacement rate. The strain-rate sensitivity exponent (m) was found to be 0.1387, slightly larger than the value predicted by Finite Element Analysis (FEA). The relationship between experimental and predicted properties from the SP tests showed a high level of agreement for maximum stress properties.
The suitability of determining the strain rate sensitivity (SRS) of the CoCrFeMnNi high-entropy alloy (HEA) by small punch (SP) testing has been assessed at displacement rates ranging from 0.2 to 2 mm center dot min(-1). The stress was found to increase as the displacement rate was raised from 0.2 to 2 mm center dot min(-1), whereas the plastic strain distributions were similar in all cases. However, for a higher displacement rate of 10 mm center dot min(-1), the sample was found to exhibit a drop in strength and ductility attributed to casting defects. The strain-rate sensitivity exponent (m) was found to be 0.1387 whilst the Finite Element Analysis (FEA) simulations predicted a slightly smaller value of 0.1313. This latter value is closer to m = 0.091 obtained from nanoindentation strain rate jump tests since the results are insensitive to the presence of small casting defects. The relationship between the experimental and the empirically derived predicted properties from the SP tests revealed a high level of agreement for maximum stress properties. The properties predicted at 2 mm center dot min(-1) (R-2 = 0.96) offered a stronger fit than at 0.5 mm center dot min(-1) (R-2 = 0.92). (c) 2022 The Authors. Published by Elsevier B.V.
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