Two-Birds-with-One-Stone Synthesis of Hydrophilic and Hydrophobic Fluorescent Carbon Nanodots from Dunaliella salina Biomass as 4-Nitrophenol Nanoprobes Based on Inner Filter Effect and First Derivative Redshift of Emission Band

Author:

Skolariki Thomais A.1ORCID,Chatzimitakos Theodoros G.1ORCID,Sygellou Lamprini2ORCID,Stalikas Constantine D.1ORCID

Affiliation:

1. Laboratory of Analytical Chemistry, Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece

2. Foundation for Research and Technology Hellas/Institute of Chemical Engineering Sciences (FORTH/ICE-HT), Stadiou Str., P.O. Box 1414, 26504 Rio-Patras, Greece

Abstract

4-Nitrophenol (4-NP) has been listed as a priority pollutant and has also been reported as a human urinary metabolite used as a marker to evaluate exposure to certain pesticides. In the work herein, a solvothermal approach is applied to the one-pot synthesis of both hydrophilic and hydrophobic fluorescent carbon nanodots (CNDs), utilizing the halophilic microalgae Dunaliella salina as a biomass precursor. Both kinds of the produced CNDs showed appreciable optical properties and quantum yields, good photostability and they were capable of probing 4-NP by quenching their fluorescence through the inner filter effect. Interestingly, a prominent 4-NP concentration-dependent redshift of the corresponding emission band of the hydrophilic CNDs was noticed, which was further exploited, for the first time, as an analytical platform. Capitalizing on these properties, analytical methods were developed and applied to a variety of matrixes, such as tap water, treated municipal wastewater and human urine. The method based on the hydrophilic CNDs (λex/λem: 330/420 nm) was linear in the range of 0.80–45.0 μM and showed acceptable recoveries (from 102.2 to 113.7%) with relative standard deviations of 2.1% (intra-day) and 2.8% (inter-day) for the quenching-based detection mode and 2.9% (intra-day) and 3.5% (inter-day) for the redshift one. The method based on the hydrophobic CNDs (λex/λem: 380/465 nm) was linear in the range of 1.4–23.0 μM, with recoveries laying within the range of 98.2–104.5% and relative standard deviations of 3.3% and 4.0% for intra-day and inter-day assays, respectively.

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

Reference45 articles.

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2. Pohanish, R.P. (2017). Sittig’s Handbook of Toxic and Hazardous Chemicals and Carcinogens, William Andrew.

3. Chromium(III)-doped carbon dots: Fluorometric detection of p-nitrophenol via inner filter effect quenching;Li;Microchim. Acta,2019

4. US EPA (1998, January 01). Reregistration Eligibility Decision (RED) Paranitrophenol, Available online: https://archive.epa.gov/pesticides/reregistration/web/pdf/2465red.pdf.

5. The separation and determination of nitrophenol isomers by high-performance capillary zone electrophoresis;Guo;Talanta,2004

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