High-Performance Ethylene Glycol Sensor Based on Imine Covalent Organic Frameworks

被引:6
|
作者
Liu, Shiwei [1 ]
Zhang, Guojie [1 ]
Zhang, Weiyu [1 ]
Tian, Ning [1 ]
Sun, Qihua [1 ]
Wu, Zhaofeng [1 ,2 ]
机构
[1] Xinjiang Key Lab Solid State Phys & Devices, Urumqi 830046, Peoples R China
[2] Xinjiang Univ, Sch Phys Sci & Technol, Urumqi 830046, Peoples R China
基金
中国国家自然科学基金;
关键词
ethylene glycol sensor; covalent organic frameworks; selectivity; long-term stability; GAS SENSORS; CRYSTALLINE;
D O I
10.3390/nano13243103
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The colorless and odorless ethylene glycol is prone to unknowingly causing poisoning, making preventive monitoring of ethylene glycol necessary. In this paper, scandium (III) trifluoromethanesulfonate was used as a catalyst to successfully prepare covalent organic framework (COF) nanospheres linked by imines at room temperature. The COF nanospheres were characterized by XRD, SEM, TEM, FT-IR, UV-Vis and BET. The results show that COF nanospheres have rough surfaces and a large number of mesoporous structures, which greatly increase the active sites on the surface of the sensing material and enhance the gas sensing performance. The sensing results showed that the prepared imine-conjugated COF nanospheres exhibited a good response-recovery ability for 10 consecutive response-recovery cycles for ethylene glycol at room temperature and had a theoretical detection limit of 40 ppb. In addition, the responses of COF nanospheres to nearly 20 interfering gases, including HCl, HNO3, phenol, formaldehyde and aniline, are relatively low compared to the response to ethylene glycol, indicating that the COF nanospheres have high selectivity towards ethylene glycol. The COF nanospheres show good sensitivity and selectivity for the detection of ethylene glycol, which should be attributed to the large specific surface area, hydrogen bonding interactions, and high defects. This work provides an effective method for the detection of ethylene glycol and expands the application field of COF materials.
引用
收藏
页数:12
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