NH2-MIL-53(Al) Metal–Organic Framework as the Smart Platform for Simultaneous High-Performance Detection and Removal of Hg2+

化学 金属有机骨架 检出限 选择性 配体(生物化学) 羧酸盐 发光 吸附 金属 Mercury(编程语言) 荧光 水溶液中的金属离子 无机化学 物理化学 催化作用 立体化学 有机化学 色谱法 生物化学 量子力学 光电子学 受体 程序设计语言 物理 计算机科学
作者
Liang Zhang,Jing Wang,Ting Du,Wentao Zhang,Wenxin Zhu,Chengyuan Yang,Tianli Yue,Jing Sun,Tao Li,Jianlong Wang
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:58 (19): 12573-12581 被引量:165
标识
DOI:10.1021/acs.inorgchem.9b01242
摘要

The worsening pollution due to mercury species makes it inevitable to explore prospective versatile materials, which not only can detect mercury ions (Hg2+) with high sensitivity but also possesses efficient capture and removal ability. In this study, a series of classic organic ligand-based luminescence MOFs materials with high oxidation state central metals (Al3+, Zr4+, Cr3+, Fe3+, and Ti4+) were synthesized and were screened to achieve simultaneously Hg2+ detection and removal through the strong coordination of amino groups or nitrogen centers with Hg2+ and the intrinsic fluorescence intensity of MOFs regulated by the ligand-to-metal charge transfer (LMCT) effect. Among these checked materials, NH2-MIL-53(Al) exhibited the excellent ability for Hg2+ detection with wide response interval (1-17.3 μM), low detection limit (0.15 μM), good selectivity, wide pH adaptation (4.0-10.0), and strong anti-interference ability. Meanwhile, the resultant NH2-MIL-53(Al) possessed an efficient removal capability toward Hg2+, accompanied by a fast uptake kinetics (within 60 min) and large loading capacity (153.85 mg g-1). Furthermore, NH2-MIL-53(Al) also displayed satisfactory stability before and after Hg2+ treatment because of the formation of strong coordination bonds between high oxidation state aluminum (Al3+) and organic carboxylate ligands. Notably, the prepared NH2-MIL-53(Al) had no significant loss of adsorption performance even after being reused four times. All of these superior properties render the smart NH2-MIL-53(Al) nanohexahedron a great potential for simultaneous Hg2+ detection and removal from water.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
wangYJ完成签到,获得积分10
1秒前
莹莹完成签到 ,获得积分10
1秒前
充电宝应助yuyuwei采纳,获得10
1秒前
lili发布了新的文献求助10
3秒前
牛马学生完成签到,获得积分10
3秒前
爆米花应助JM采纳,获得30
3秒前
年年完成签到,获得积分20
3秒前
哭泣绿旋完成签到,获得积分10
4秒前
Ava应助m李采纳,获得10
4秒前
4秒前
Lau完成签到,获得积分20
8秒前
tq完成签到,获得积分10
8秒前
一只羊完成签到 ,获得积分10
8秒前
量子星尘发布了新的文献求助10
9秒前
嘟嘟完成签到 ,获得积分10
9秒前
10秒前
Akim应助李昕123采纳,获得20
10秒前
地理汪汪发布了新的文献求助10
10秒前
11秒前
在水一方应助lili采纳,获得10
11秒前
诺坎普的晚风完成签到,获得积分20
11秒前
13秒前
浮游应助料峭声花采纳,获得10
13秒前
JamesPei应助明白放弃采纳,获得10
14秒前
14秒前
WWW完成签到 ,获得积分10
15秒前
酸酸给酸酸的求助进行了留言
16秒前
18秒前
18秒前
lijiauyi1994发布了新的文献求助10
19秒前
19秒前
lili完成签到,获得积分10
21秒前
Lucas应助vayne采纳,获得10
21秒前
有魅力的沧海完成签到 ,获得积分10
22秒前
科研通AI6应助地理汪汪采纳,获得10
22秒前
lll发布了新的文献求助20
23秒前
所所应助白三采纳,获得10
23秒前
xiaoyao完成签到,获得积分10
24秒前
JiuYu发布了新的文献求助10
24秒前
yang完成签到,获得积分20
24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
The Social Work Ethics Casebook: Cases and Commentary (revised 2nd ed.).. Frederic G. Reamer 1070
Alloy Phase Diagrams 1000
Introduction to Early Childhood Education 1000
2025-2031年中国兽用抗生素行业发展深度调研与未来趋势报告 1000
List of 1,091 Public Pension Profiles by Region 871
Synthesis and properties of compounds of the type A (III) B2 (VI) X4 (VI), A (III) B4 (V) X7 (VI), and A3 (III) B4 (V) X9 (VI) 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5422108
求助须知:如何正确求助?哪些是违规求助? 4537012
关于积分的说明 14155721
捐赠科研通 4453595
什么是DOI,文献DOI怎么找? 2442968
邀请新用户注册赠送积分活动 1434374
关于科研通互助平台的介绍 1411439