期刊
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
卷 210, 期 -, 页码 398-404出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2018.08.048
关键词
Diazo-coupling reaction; p-Aminobenzoic acid; Phloroglucinol; Acid medium; Diazonium ion; Azo dye
类别
资金
- National Natural Science Foundation of China [21575115, 21327005, 21665023, 21565021]
- Program for Chang Jiang Scholars, Ministry of Education, China [IRT-16R61, 2017D-01]
- Program of Innovation and Entrepreneurial for Talent, Lanzhou, Gansu Province, China [2014-RC-39]
Immoderate intake of nitrite (NO2-) is deleterious human health and may result in causing dangerous diseases. In this study, nitrite detection system was successfully fabricated based on a unique diazo-coupling reaction of p-Aminobenzoic acid (PABA) and phloroglucinol (1, 3, 5-trihydroxybenzene). Upon the presence of NO2- in an acid medium, p-Aminobenzoic acid could not only form diazonium ion easily but also couple with p-Aminobenzoic acid, and results forming yellow water-soluble azo dye that shows maximum absorption at 434 nm. Under the further accurate determination condition, such as acid concentration, amount of reagents and time required, the naked-eye detection of NO2- showed excellent selectivity in compared with some anions. Especially, diazotization and coupling reaction proposed here is very fast and control of pH and temperature are unnecessary. Moreover, the color is stable for several days and Beer's law is obeyed over a wide range. Reliable detection can be made in the range of 0.05 to 1 p.p.m. of nitrite ion. Detection limit was calculated to be 0.024 p.p.m. (0.521 mu M) by UV-visible spectroscopy and 0.05 p.p.m. (1.091 mu M) by naked-eye. By using an electrochemical method, IR, SEM, and (HNMR)-H-1, the sensing mechanism can be easily verified. More importantly the proposed method was successfully applied for the determination of nitrite in a real water sample. (C) 2018 Elsevier B.V. All rights reserved.
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