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首页> 外文期刊>Journal of Nuclear Materials: Materials Aspects of Fission and Fusion >In-situ TEM study of radiation-induced amorphization and recrystallization of hydroxyapatite
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In-situ TEM study of radiation-induced amorphization and recrystallization of hydroxyapatite

机译:辐射诱导的羟基磷灰石的原位TEM研究和再结晶的羟基磷灰石

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The radiation response of hydroxyapatite, a nuclear waste form candidate, was investigated using 1 MeV Kr2+ and 200 keV electron irradiations combined with in-situ TEM observation. The results showed a remarkable difference in the behavior of nano-crystalline hydroxyapatite under the two different radiation conditions. A crystalline-to-amorphous transformation occurred under the 1 MeV Kr2+ irradiation due to the accumulation of displacement damage, with a critical amorphization dose (Dc) of 2 x 10(14) ions/cm(2) (0.05 dpa) at room temperature. The Dc increased dramatically with temperature due to effective dynamic annealing of radiation-induced defects, such that no amorphization occurred above a critical temperature (Tc) of 545 K. In contrast, under 200 keV electron irradiation, which mainly dissipates its energy through inelastic ionization processes, the pre-amorphized hydroxyapatite exhibited rapid recrystallization, likely due to the bond breaking and reforming at the amorphous-crystalline interface assisted by the ionization. The electron-irradiation induced recrystallization in amorphous hydroxyapatite was extremely sensitive, with a critical electron dose several orders of magnitude lower than most previously reported ceramics. Under concurrent ion and electron irradiations, the materials retained crystalline even at the critical dose of 0.05 dpa, and remained so until the dose reached 0.15 dpa, lending further proof to the enhanced defect recovery by ionizing electrons. The radiation data of hydroxyapatite highlights the material's sensitivity to radiation conditions and its excellent dynamic defect annealing ability. (C) 2018 Elsevier B.V. All rights reserved.
机译:使用1MeV KR2 +和200KeV电子照射研究了羟基磷灰石,核废料表候选候选核废料表候选的辐射响应,与原位TEM观察结合。结果表明,在两个不同的辐射条件下纳米结晶羟基磷灰石的行为差异显着。由于位移损伤的积累,在1meV KR2 +辐射下发生结晶至无定形的转变,在室温下具有2×10(14)离子/ cm(2)(0.05dPa)的临界美态化剂量(DC) 。由于辐射诱导的缺陷的有效动态退火,DC随着温度而显着增加,使得在545k的临界温度(Tc)上没有发生任何态化。相反,在200keV电子照射下,这主要通过非弹性电离来消散其能量。方法,预混物羟基磷灰石表现出快速重结晶,可能是由于通过电离辅助的无定形结晶界面处的粘合和重整的粘合和重整。无定形羟基磷灰石中的电子照射诱导的重结晶是极其敏感的,具有关键的电子剂量,几个数量级低于大多数先前报告的陶瓷。在并发离子和电子照射下,即使在0.05dPa的临界剂量为0.05dPa的临界剂量,仍保持晶体的材料,直至给剂量达到0.15dPa,通过电离电子进一步证明增强缺陷恢复。羟基磷灰石的辐射数据突出了材料对辐射条件的敏感性及其优异的动态缺陷退火能力。 (c)2018年elestvier b.v.保留所有权利。

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