Simple and sensitive determination of trace nitrite in water by zero-crossing first-derivative synchronous fluorescence spectrometry using 6-amino-1,3- naphthalenedisulfonic acid as a new fluorescent probe

التفاصيل البيبلوغرافية
العنوان: Simple and sensitive determination of trace nitrite in water by zero-crossing first-derivative synchronous fluorescence spectrometry using 6-amino-1,3- naphthalenedisulfonic acid as a new fluorescent probe
المؤلفون: Di Zuo, Run-Ye Yang, Ya-Feng Zhuang, Gui-Ping Cao, Yanhua Wang
المصدر: Analytical and bioanalytical chemistry. 409(19)
سنة النشر: 2016
مصطلحات موضوعية: Detection limit, 010401 analytical chemistry, Analytical chemistry, Hydrochloric acid, 02 engineering and technology, 021001 nanoscience & nanotechnology, Mass spectrometry, 01 natural sciences, Biochemistry, Fluorescence, Spectral line, 0104 chemical sciences, Analytical Chemistry, chemistry.chemical_compound, chemistry, Sodium hydroxide, Nitrite, 0210 nano-technology, Excitation
الوصف: A new fluorescent probe, 6-amino-1,3-naphthalenedisulfonic acid (ANDSA), has been developed for the determination of trace nitrite in different waters. This probe is based on the selective reaction of nitrite with ANDSA in hydrochloric acid solution to form the corresponding diazonium acid in sodium hydroxide solution at room temperature. The diazonium acid produced has high fluorescence intensity at 488 nm (excitation at 367 nm), whereas ANDSA has high fluorescence intensity at 465 nm (excitation at 354 nm). The synchronous fluorescence (Δλ = 121 nm) spectrum and the first-derivative synchronous fluorescence spectrum of diazonium acid greatly overlapped with those of ANDSA. The zero-crossing method was used to measure the first-derivative value (dF/dλ) of the first-derivative spectra, in which physical separation of excess ANDSA was unnecessary. The zero-crossing point was located at 351.2 nm for ANDSA, at which dF/dλ of diazonium acid was proportional to the nitrite concentration. Therefore, dF/dλ at 351.2 nm was selected as the analytical signal. Under the optimized experimental conditions, the signal intensity was linear over a nitrite concentration range of 0.006–0.075 mg L−1, with a correlation coefficient better than 0.9994. The limit of detection was 2.1 μg L−1 for the determination of nitrite by the proposed method. The relative standard deviation of the method for the determination of nitrite in real water samples was below 2.45%, and the corresponding recoveries were between 95.7% and 104.1%. The validity of the proposed method was further confirmed by comparison with the reference method with use of the t test.
تدمد: 1618-2650
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b666fea573196f53b09861acd357f3e
https://pubmed.ncbi.nlm.nih.gov/28573318
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....5b666fea573196f53b09861acd357f3e
قاعدة البيانات: OpenAIRE