Abstract

The temperature dependence of helium bubble evolution in 316L stainless steel (SS) fabricated by selective laser melting (SLM) has been studied by performing 500 keV helium ion irradiation at temperatures between 350 and 900 °C. The number density of helium bubbles decreased steadily whereas the bubble diameter gradually increased with increasing temperature. The material swelling caused by helium bubbles had no obvious change at the temperature below 800 °C. However, at the maximum temperature of 900 °C, the swelling sharply increased to 0.17% mainly due to the rapidly growing bubble diameter. In particular, heterogeneous nucleation of bubbles occurred in the vicinity of dislocation structures at high temperatures of 700–900 °C, and the formed helium bubbles rapidly grew at the oxide-matrix interface at 900 °C. It was confirmed various intrinsic structures (dislocation structures or oxide particles) differently affected the bubble evolution process. The apparent activation energy (Eact) of helium bubbles determined by the Arrhenius model were used to elucidate the most probable helium bubble evolution mechanisms at various temperatures, as it is an experimentally observed activation energy, which contained information about the activity of helium atoms. It was found that the low-temperature regime with low apparent activation energies (ECbact=0.15eV,ERbact=0.04eV) and high-temperature regime with high apparent activation energies (ECbact=1.50eV,ERbact=0.58eV) favored different helium bubble evolution mechanisms. In the low-temperature regime, helium bubble evolution was controlled by the diffusion of helium atoms via a vacancy mechanism in the SLM 316L SS. On the other hand, the migration and coalescence of helium bubbles also occurred in the high-temperature regime which caused the apparent activation energy of density was higher than the theoretical value of helium atoms diffuse via a replacement mechanism.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call