Mesoporous silica imprinted carbon dots for the selective fluorescent detection of triclosan

被引:29
作者
Bhogal, Shikha [1 ]
Mohiuddin, Irshad [2 ]
Malik, Ashok Kumar [1 ]
Brown, Richard J. C. [3 ]
Heynderickx, Philippe M. [4 ,5 ]
Kim, Ki-Hyun [6 ]
Kaur, Kuldeep [7 ]
机构
[1] Punjabi Univ, Dept Chem, Patiala 147002, Punjab, India
[2] Panjab Univ, Dept Chem, Sect 14, Chandigarh 160014, India
[3] Natl Phys Lab, Atmospher Environm Sci Dept, Hampton Rd, Teddington TW11 0LW, Middx, England
[4] Ghent Univ Global Campus, CEER, Engn Mat Via Catalysis & Characterizat, 119-5 Songdomunhwa Ro, Incheon 406840, South Korea
[5] Univ Ghent, Fac Biosci Engn, Dept Green Chem & Technol, Coupure Links 653, B-9000 Ghent, Belgium
[6] Hanyang Univ, Dept Civil & Environm Engn, Seoul 04763, South Korea
[7] Mata Gujri Coll, Dept Chem, Fatehgarh Sahib 140407, India
基金
新加坡国家研究基金会;
关键词
Carbon dots; Mesoporous silica; Imprinted polymer; Triclosan; Fluorescent sensor; electron transfer induced mechanism; CDTE QUANTUM DOTS; WASTE-WATER; POLYMER; SENSOR; PROBE; IONS;
D O I
10.1016/j.scitotenv.2022.157289
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A molecularly imprinted fluorescence sensor built as a mesoporous structured silica imprinted layer on the surface of carbon dots (CDs@m-MIP) was employed for the selective detection of triclosan (TRI). The fluorescence of this CDs@m-MIP was affected sensitively and selectively by TRI via an electron transfer-induced fluorescence quenching mechanism with a detection limit of TRI at 1.08 nM(range 1.72-138 nM) under the optimum setup (e.g., pH, response time, and CDs@m-MIP dose). This approach was used successfully to detect TRI in real water samples (e.g., sewage, river, and tap water). The recoveries of TRI were satisfactory in spiked river and tap water (in 94.7-99.5 %). The outcome of this research is thus expected to help develop highly efficient fluorescent sensing systems towards diverse hazardous compounds including TRI.
引用
收藏
页数:10
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