对氧磷
纳米复合材料
检出限
降级(电信)
荧光
材料科学
核化学
酶
纳米技术
化学
分析化学(期刊)
色谱法
有机化学
乙酰胆碱酯酶
电信
物理
量子力学
计算机科学
作者
Bo Liu,Meijie Cai,Xiangling Feng,Siyu Lu,Song Lin,Feng Tian
出处
期刊:Carbon
[Elsevier]
日期:2023-06-01
卷期号:209: 118003-118003
被引量:5
标识
DOI:10.1016/j.carbon.2023.118003
摘要
Serial nanocomposites consisting of blue fluorescent carbon dots (B-CDs) and MgO nanoparticles were facilely prepared. Then on-site detection and degradation of ethyl-paraoxon were achieved and evaluated. It was revealed that ethyl-paraoxon was firstly decomposed into p-nitrophenol by MgO. Then, p-nitrophenol could significantly quench the fluorescence of decorated B-CDs due to an inner filter effect (IFE). The [email protected] showed excellent comprehensive performance among the serial [email protected] samples due to its relatively high degradation ability towards ethyl-paraoxon and potent initial fluorescence emission intensity at an excitation wavelength of 360 nm between pH 4 and 10. Finally, based on the IFE, on-site paper sensors via color recognition app on a smartphone were explored compared with a conventional fluorescence spectrometer. Both the quantitative fluorescence intensities and G/B values showed the multi-piecewise linear correlations to ethyl-paraoxon concentration up to 3000 μg/mL in river water with a limit of detection to 0.06 μg/mL and 3.48 μg/mL as well as high recovery rates between 99%-102% and 95%–116%, respectively. The in vitro cytotoxicity and phytotoxicity assessment of the [email protected] revealed dose-dependent effects. Such portable and integrated fluorescent [email protected] nanocomposites on paper arrays show excellent potential in shortening the detection time and reducing the detection cost as a new strategy for the on-site quantitative detection and degradation of ethyl-paraoxon in actual river water.
科研通智能强力驱动
Strongly Powered by AbleSci AI