Novel reduced-activation TiVCrFe based high entropy alloys

灰烬 高熵合金 Laves相 五元 材料科学 金属间化合物 微观结构 合金 冶金 相(物质) 热力学 铸造 固溶体 数据库 相图 化学 计算机科学 物理 有机化学
作者
A.W. Carruthers,Boya Li,M. Rigby,L.C. Raquet,R. Mythili,C. Ghosh,Arup Dasgupta,David E.J. Armstrong,Amy S. Gandy,E.J. Pickering
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:856: 157399-157399 被引量:44
标识
DOI:10.1016/j.jallcom.2020.157399
摘要

The conditions inside next-generation nuclear reactors are likely to be extreme. High-performance materials will be required, and there is still great scope for developing new and improved alloys. High-entropy alloys (HEAs) are potential candidates, and it is likely that such alloys will need to be based around low-activation elements that tend to form body-centred cubic structures. Whilst there have been a number of investigations assessing the capability of CALPHAD databases to predict the phases formed in face-centred cubic HEAs, their applicability to less studied systems is not well known. Here, two low-activation HEAs are produced; TiVCrMnFe and Si0.1TiVCr0.5Fe, and their microstructures assessed and compared to CALPHAD predictions. The microstructures of both alloys comprised a C14 Laves phase and a B2 phase following casting, and a C14 Laves phase and a BCC solid solution (A2) phase following holding at 1200 °C, with high proportions of both constituent phases found in each case. It was found experimentally that the Laves phases in both alloys were quaternary intermetallics of Fe, V, Cr and Ti, with Fe, V and Cr likely disordered across the Fe site. These observations were compared with predictions made using four CALPHAD databases. The accuracy of the predictions varied markedly between the databases. It was found that the Laves phase was underpredicted, often severely, by the databases that did not account for the quinary nature of phase. Removing Ti from TiVCrMnFe resulted in an equiatomic VCrMnFe alloy that formed a single BCC phase at 1200 °C.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
烟花应助天涯勿忘归采纳,获得10
2秒前
huiii发布了新的文献求助10
5秒前
竹萧发布了新的文献求助10
6秒前
复杂易形发布了新的文献求助10
6秒前
6秒前
鲁万仇发布了新的文献求助20
8秒前
12秒前
寒冷荧荧完成签到 ,获得积分10
15秒前
五颗星完成签到 ,获得积分10
16秒前
17秒前
冯堆堆发布了新的文献求助20
19秒前
六十变九十完成签到,获得积分10
19秒前
秋白完成签到,获得积分10
20秒前
传统的妖妖完成签到,获得积分20
20秒前
20秒前
一颗奇异果完成签到,获得积分10
23秒前
23秒前
笨笨山芙发布了新的文献求助10
23秒前
猫念初完成签到,获得积分10
24秒前
天涯勿忘归完成签到,获得积分10
24秒前
我谈完成签到,获得积分10
24秒前
HEH完成签到,获得积分10
25秒前
25秒前
Bubu完成签到,获得积分10
26秒前
27秒前
端木落月mc完成签到,获得积分10
28秒前
28秒前
DOC_XIONG应助复杂易形采纳,获得10
29秒前
29秒前
阿白完成签到,获得积分10
30秒前
摸鱼大王在摸鱼完成签到 ,获得积分10
31秒前
ljb完成签到,获得积分10
33秒前
waerteyang发布了新的文献求助10
34秒前
竹萧完成签到,获得积分10
35秒前
天天快乐应助海绵宝宝采纳,获得10
38秒前
qiaoxixi发布了新的文献求助10
40秒前
晚塬完成签到 ,获得积分10
42秒前
十万只皮卡丘完成签到,获得积分10
45秒前
qiaoxixi完成签到,获得积分10
47秒前
fly完成签到,获得积分10
48秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
A Psychological Understanding of Criticism and Mental Health 600
Organizational Behavior 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7750947
求助须知:如何正确求助?哪些是违规求助? 9298459
关于积分的说明 20246492
捐赠科研通 7333169
什么是DOI,文献DOI怎么找? 3309788
关于科研通互助平台的介绍 2461340
邀请新用户注册赠送积分活动 2322324