TY - JOUR
T1 - Rapid and Facile Organic Ion-Associate Liquid-Phase Extraction and Spectrophotometric Quantification of Nitrite in Environmental Water Samples
AU - Hata, Noriko
AU - Minoshima, Kazuki
AU - Ito, Kei
AU - Kohama, Nozomi
AU - Sazawa, Kazuto
AU - Osada, Sachiko
AU - Okazaki, Takuya
AU - Taguchi, Shigeru
AU - Kuramitz, Hideki
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/3
Y1 - 2025/3
N2 - Nitrite is a health and environmental hazard and pollutes water sources globally, but sensitive, rapid, and facile quantification methods are lacking. Herein, we report a method for extracting and quantifying low-concentration nitrite in surface water using minimal sample and solvent volumes. The nitrite reacted with sulfanilamide and N-1-naphthylethylenediammonium dichloride (NED), yielding an azo dye for extraction into an organic ion-associate liquid phase (IALP) formed in situ using ethylhexyloxypropylammonium and dodecyl sulfate ions. The addition of sodium acetate increased the pH, decreasing the cation charge from +2 to +1, improving extraction efficiency. Further, adding NaCl doubled the IALP volume, reduced the required standing time, and minimally affected absorbance, and adding concentrated HCl to the IALP enhanced the absorbance intensity via dye protonation. Crucially, the method achieved a 30-fold concentration factor compared to traditional pre-treatment methods, even without centrifugation, as well as a limit of detection of 0.09 µg NO2-N/L. Spiked recovery tests with river and seawater samples (93–103%) matched those of established methods. Digital imaging of IALP-extracted lake water yielded a limit of detection of 0.4 µg NO2-N/L. The method is a sensitive, efficient approach for nitrite detection, enabling rapid environmental monitoring via spectrophotometry and digital imaging.
AB - Nitrite is a health and environmental hazard and pollutes water sources globally, but sensitive, rapid, and facile quantification methods are lacking. Herein, we report a method for extracting and quantifying low-concentration nitrite in surface water using minimal sample and solvent volumes. The nitrite reacted with sulfanilamide and N-1-naphthylethylenediammonium dichloride (NED), yielding an azo dye for extraction into an organic ion-associate liquid phase (IALP) formed in situ using ethylhexyloxypropylammonium and dodecyl sulfate ions. The addition of sodium acetate increased the pH, decreasing the cation charge from +2 to +1, improving extraction efficiency. Further, adding NaCl doubled the IALP volume, reduced the required standing time, and minimally affected absorbance, and adding concentrated HCl to the IALP enhanced the absorbance intensity via dye protonation. Crucially, the method achieved a 30-fold concentration factor compared to traditional pre-treatment methods, even without centrifugation, as well as a limit of detection of 0.09 µg NO2-N/L. Spiked recovery tests with river and seawater samples (93–103%) matched those of established methods. Digital imaging of IALP-extracted lake water yielded a limit of detection of 0.4 µg NO2-N/L. The method is a sensitive, efficient approach for nitrite detection, enabling rapid environmental monitoring via spectrophotometry and digital imaging.
KW - azo dye
KW - chloride effect
KW - environmental monitoring
KW - in situ solvent formation
KW - without centrifugation
UR - http://www.scopus.com/inward/record.url?scp=86000804158&partnerID=8YFLogxK
U2 - 10.3390/molecules30051044
DO - 10.3390/molecules30051044
M3 - 学術論文
C2 - 40076270
AN - SCOPUS:86000804158
SN - 1420-3049
VL - 30
JO - Molecules
JF - Molecules
IS - 5
M1 - 1044
ER -