4.6 Article

Spectrophotometric method for determination of aluminium content in water and beverage samples employing flow-batch sequential injection system

期刊

JOURNAL OF FOOD COMPOSITION AND ANALYSIS
卷 41, 期 -, 页码 45-53

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jfca.2015.02.002

关键词

Flow-batch analysis; Sequential injection; Monosegmented flow analysis; Spectrophotometry; Aluminium; Eriochrome cyanine R; Water; Beverage; Food analysis; Food composition; Food safety; Heavy metals in food chain; Food safety and Heavy metals in food chain

资金

  1. Faculty of Science, Mahasarakham University [MSU-SC-2557/006/57]
  2. Mahasarakham University Development Fund
  3. Office of the Higher Education Commission
  4. Ministry of Education
  5. Thailand Research Fund (TRF)
  6. Royal Golden jubilee Ph.D. Program
  7. Center of Excellence on Innovation in Analytical Science and Technology (I-ANALY-ST), Chiang Mai University
  8. Center of Excellence for Innovation in Chemistry (PERCH-CIC)

向作者/读者索取更多资源

A sensitive, precise and reliable flow-batch method for the determination of aluminium (Al) was developed using a sequential injection-monosegmented flow system incorporating a mixing chamber unit. Eriochrome cyanine R (ECR) was used as a chromogenic reagent in the presence of N,N-dodecyltrimethylammonium bromide (DTAB). The Al-ECR complex at pH 6 gave a maximum absorption at 584 nm. In-line single standard calibration and a standard addition procedure were developed employing the monosegmented flow technique. Under the optimum conditions, a linear calibration graph in the range of 0.0075-0.625 mg L-1 Al was obtained with limits of detection and quantitation of 0.0020 and 0.0070 mg L-1, respectively. Relative standard deviations were 0.8 and 1.3% for 0.010 and 0.025 mg L-1 Al (n = 11), respectively. A sample throughput of 24 h(-1) using an in-line standard calibration approach and 6 h-1 using four standard addition levels was achieved. The developed system was successfully applied to water samples and beverage samples. The results agreed well with those obtained from the ICP-AES method. Good recoveries between 85 and 104% were obtained. (C) 2015 Elsevier Inc. All rights reserved.

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