Exploiting an automated microfluidic hydrodynamic sequential injection system for determination of phosphate

被引:21
|
作者
Khongpet, Wanpen [1 ]
Pencharee, Somkid [2 ]
Puangpila, Chanida [1 ]
Hartwell, Supaporn Kradtap [3 ]
Lapanantnoppakhun, Somchai [1 ]
Jakmunee, Jaroon [1 ,4 ,5 ]
机构
[1] Chiang Mai Univ, Fac Sci, Dept Chem, Lab Analyt Instrumentat & Electrochem Innovat, Chiang Mai 50200, Thailand
[2] Ubon Ratchathani Univ, Dept Phys, Fac Sci, Ubon Ratchathani 34190, Thailand
[3] Xavier Univ, Dept Chem, 3800 Victory Pkwy, Cincinnati, OH 45207 USA
[4] Chiang Mai Univ, Fac Sci, Ctr Environm Sci, Chiang Mai 50200, Thailand
[5] Chiang Mai Univ, Fac Sci, Ctr Excellence Innovat Chem, Chiang Mai 50200, Thailand
关键词
Microfluidic; Hydrodynamic sequential injection HSI; Phosphate; Molybdenum blue; Soil; MOLYBDENUM BLUE REACTION; WASTE-WATER; SILICATE; ORTHOPHOSPHATE; PHOSPHORUS; NITRATE; MANIFOLD; SOILS;
D O I
10.1016/j.talanta.2017.09.018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A microfluidic hydrodynamic sequential injection (HSI) spectrophotometric system was designed and fabricated. The system was built by laser engraving a manifold pattern on an acrylic block and sealing with another flat acrylic plate to form a microfluidic channel platform. The platform was incorporated with small solenoid valves to obtain a portable setup for programmable control of the liquid flow into the channel according to the HSI principle. The system was demonstrated for the determination of phosphate using a molybdenum blue method. An ascorbic acid, standard or sample, and acidic molybdate solutions were sequentially aspirated to fill the channel forming a stack zone before flowing to the detector. Under the optimum condition, a linear calibration graph in the range of 0.1-6 mg P L-1 was obtained. The detection limit was 0.1 mg L-1. The system is compact (5.0 mm thick, 80 mm wide x 140 min long), durable, portable, cost-effective, and consumes little amount of chemicals (83 mu L each of molybdate and ascorbic acid, 133 mu L of the sample solution and 1.7 mL of water carrier/run). It was applied for the determination of phosphate content in extracted soil samples. The percent recoveries of the analysis were obtained in the range of 91.2-107.3. The results obtained agreed well with those of the batch spectrophotometric method.
引用
收藏
页码:77 / 85
页数:9
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