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A novel turn-on fluorescent sensor for the detection of ascorbic acid (AA) has been developed based on the fluorescence resonance energy transfer (FRET) between graphene quantum dots (GQDs) and squaric acid (SQA)-iron(iii). In this assay, iron(iii) can rapidly coordinate with the SQA to produce SQA-iron(iii). The absorbance band of SQA-iron(iii) could be largely overlapped with the emission band of GQDs, thus resulting in the fluorescence resonance energy transfer (FRET)-induced fluorescence quenching of GQDs. Moreover, the fluorescence of GQDs can be sensitively turned on by AA through the oxidation-reduction between iron(iii) and AA. After the transformation of SQA-iron(iii) to SQA-iron(ii), because the absorbance of the solution reduces, the FRET decreases. This FRET-based nanosensor shows high selective and sensitive response in the concentration of AA ranging from 1.0 to 95 μM with the detection limit as lower as 200 nM, which is lower than that of other fluorescent assays. Finally, the proposed sensing system was successfully applied to the direct analysis of AA in the real samples with satisfactory results.

In this work, magnetic fluorescence molecularly imprinted microspheres were prepared for recognition and separation of 4-nonylphenol. The prepared composite was evaluated and characterized in detail by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, fluorescence spectroscopy, fluorescence microscopy, vibrating sample magnetometry, and X-ray diffraction analyses. The results showed that the composite exhibited a uniform spherical shape and a core–shell structure. Moreover, this hybrid had a saturation magnetization value of 4.79 emu g−1, which provided an efficient way to separate toxic pollutants from extreme environments. And, the hybrid had the recognition ability for 4-nonylphenol by the changes of fluorescence signals, owning to the intrinsic fluorescent properties. Furthermore, the imprinting factor (IF) reached 2.37, which proved that many specific recognition sites with respect to the template were generated on the surface of MIPs and outstanding binding affinity and recognition selectivity towards 4-nonylphenol over competitive phenolic compounds.