A violet light-emitting diode-based gas-phase molecular absorption device for measurement of nitrate and nitrite in environmental water

被引:2
|
作者
Liu, Chuanyu [1 ]
Gao, Shuo [1 ]
Han, Xiaoxuan [2 ,3 ]
Tian, Yong [1 ]
Ma, Jiping [1 ]
Wang, Weiliang [1 ]
Chen, Xu-Wei [2 ,3 ]
Chen, Ming-Li [2 ,3 ]
Zhang, Yanfeng [4 ]
机构
[1] Qingdao Univ Technol, Sch Environm & Municipal Engn, Qingdao 266033, Peoples R China
[2] Northeastern Univ, Res Ctr Analyt Sci, Shenyang 110819, Peoples R China
[3] Northeastern Univ, Coll Sci, Dept Chem, Shenyang 110819, Peoples R China
[4] Intelligent Policing Key Lab Sichuan Prov, Luzhou 646000, Peoples R China
基金
中国国家自然科学基金;
关键词
Gas -phase molecular absorption spectrometry; Nitrite; Nitrate; Violet light -emitting diode; Field measurement; CAPILLARY-ZONE-ELECTROPHORESIS; BIOLOGICAL-FLUIDS; CHROMATOGRAPHY; CHEMILUMINESCENCE; EXPOSURE; NITROGEN; SAMPLES; ACID;
D O I
10.1016/j.saa.2024.124423
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
A simple and sensitive device for the detection of nitrite and nitrate in environmental waters was developed based on visible light gas-phase molecular absorption spectrometry. By integrating a detection cell (DC), semiconductor refrigeration temperature-controlling system (SRTCY), and nitrite reactor into a sequential injection analysis system, trace levels of nitrite and nitrate in complex matrices were successfully measured. A low energyconsuming light-emitting diode (violet, 400-405 nm) was coupled with a visible light-to-voltage converter (TSL257) to measure the gas-phase molecular absorption. To reduce the interference of water vapor, an SRTCY was used to condense the water vapor on-line before the gas-phase analyte entered the DC. The DC was radiatively heated by the SRTCY to avoid water vapor condensation in the light path. As a result, the obtained baseline noise reduced 3.75 times than that of without SRTCY. Under the optimized conditions, the device achieved limits of detection (3 sigma/k) of 0.055 and 0.36 mmol/L (0.77 and 5.04 mg N/L) for nitrite and nitrate, respectively, and the linear calibration ranges were 0.1-15 mmol/L (R2 = 0.9946) and 1-10 mmol/L (R2 = 0.9995), respectively. Precisions of 5.2 % and 9.0 % were achieved for ten successive determinations of 0.3 mmol/L nitrite and 1.0 mmol/L nitrate, and the analytical times for nitrite and nitrate determination were 5 and 13 min, respectively. This method was validated against standard methods and recovery tests, and it was applied to the measurement of nitrite and nitrate in environmental waters. Moreover, a device was designed to enable the field measurement of nitrite and nitrate in complex matrices.
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页数:7
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