Feasibility Study of Using Bi-mna Metal–Organic Frameworks as Adsorbents for Radioiodine Capture at High Temperature

吸附 热重分析 金属有机骨架 化学吸附 化学 沸石咪唑盐骨架 X射线光电子能谱 材料科学 无机化学 化学工程 物理化学 有机化学 工程类
作者
Young-Eun Jung,Seong-Woo Kang,Man‐Sung Yim
出处
期刊:Industrial & Engineering Chemistry Research [American Chemical Society]
卷期号:60 (16): 5964-5975 被引量:25
标识
DOI:10.1021/acs.iecr.1c00450
摘要

In this study, a bismuth-based metal–organic framework (Bi-MOF) was investigated in its applicability as an iodine adsorbent at high temperatures for possible applications under severe accidents in a nuclear power plant. Bi-mna was selected among Bi-MOF candidates based on its thermodynamic characteristics, which expected to allow chemisorption of iodine by bismuth. Its iodine adsorption performance was compared with zeolitic imidazolate framework-8 and Cu-BTC and other MOFs which were chosen due to their diversity in iodine adsorption mechanisms. Bi-mna was synthesized at the laboratory scale, and the aforementioned three MOFs were tested for iodine adsorption at various temperatures from 350 to 600 K. The adsorption mechanism of Bi-mna was investigated by conducting various analyses including thermogravimetric analysis, X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller. The results showed that Bi-mna has good adsorption performance (700 mg-I/g-adsorbent) while maintaining good thermal stability even at a high temperature (up to 575–600 K). The iodine capture performance of Bi-mna is better, especially at high temperature, in comparison with those of non-MOF adsorbents such as silver-exchanged zeolites and bismuth-embedded SBA-15. Analysis results confirmed that Bi-mna chemically captured iodine by breaking bonds between bismuth and sulfur to form new chemical bonds between iodine and the bismuth in Bi-mna. The results indicate that Bi-mna has the potential to be used in capturing radioiodine at high-temperature environments, such as during nuclear severe accident management. Its use should also be considered as a potential candidate for waste form development.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
一直在笑发布了新的文献求助10
刚刚
1秒前
1秒前
科研通AI2S应助xde的玩偶采纳,获得10
1秒前
DAN发布了新的文献求助10
1秒前
魔刹石完成签到,获得积分10
2秒前
2秒前
直率的惜寒完成签到,获得积分10
2秒前
七七发布了新的文献求助10
3秒前
4秒前
4秒前
重要千青完成签到,获得积分10
4秒前
孤独念柏完成签到 ,获得积分10
5秒前
傅。完成签到 ,获得积分10
5秒前
Yanice_Wan关注了科研通微信公众号
6秒前
桐桐应助bb采纳,获得10
6秒前
小不溜完成签到,获得积分10
7秒前
Dore应助微微采纳,获得20
7秒前
sstt发布了新的文献求助10
8秒前
沉默的羔手完成签到 ,获得积分10
8秒前
xu发布了新的文献求助10
9秒前
隐形曼青应助肉肉的肉采纳,获得10
9秒前
汉堡包应助努力的白痴采纳,获得10
10秒前
江汉小龙完成签到,获得积分10
10秒前
庄默羽发布了新的文献求助10
10秒前
祝一二三四完成签到,获得积分10
10秒前
0055应助dagongren采纳,获得10
11秒前
花花又子完成签到 ,获得积分10
11秒前
zhaiping完成签到,获得积分10
12秒前
Finneen完成签到,获得积分10
12秒前
聂裕铭完成签到 ,获得积分10
13秒前
13秒前
早晚完成签到 ,获得积分10
14秒前
复杂涵柏完成签到,获得积分10
14秒前
时光完成签到,获得积分10
15秒前
简凤银发布了新的文献求助10
15秒前
庞威完成签到 ,获得积分10
15秒前
跳跃仙人掌应助zhouleiwang采纳,获得10
15秒前
科研通AI2S应助kopew采纳,获得10
17秒前
McchainQ发布了新的文献求助10
18秒前
高分求助中
One Man Talking: Selected Essays of Shao Xunmei, 1929–1939 1000
A Chronicle of Small Beer: The Memoirs of Nan Green 1000
From Rural China to the Ivy League: Reminiscences of Transformations in Modern Chinese History 900
Migration and Wellbeing: Towards a More Inclusive World 900
Eric Dunning and the Sociology of Sport 850
Operative Techniques in Pediatric Orthopaedic Surgery 510
The Making of Détente: Eastern Europe and Western Europe in the Cold War, 1965-75 500
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 免疫学 细胞生物学 电极
热门帖子
关注 科研通微信公众号,转发送积分 2911640
求助须知:如何正确求助?哪些是违规求助? 2546862
关于积分的说明 6892826
捐赠科研通 2211796
什么是DOI,文献DOI怎么找? 1175299
版权声明 588140
科研通“疑难数据库(出版商)”最低求助积分说明 575729