TY - JOUR
T1 - Speciation of chromium in water samples using microfluidic paper-based analytical devices with online oxidation of trivalent chromium
AU - Muhammed, Abdellah
AU - Hussen, Ahmed
AU - Kaneta, Takashi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Numbers JP19H04675 and JP20H02766.
Funding Information:
The authors thank Addis Ababa University Thematic Research Fund for supporting the project titled “Developing Innovative Microfluidic Paper-Based Analytical Devices (μ-PADs): Viable solution for Environmental Monitoring in Ethiopia” at the Center for Environmental Science. A. M. also acknowledges Wollo University and Okayama University for providing him with a Ph. D. study leave and with the opportunity of working for the Ph. D. study, respectively. The authors gratefully thank Division of Instrumental Analysis, Department of Instrumental Analysis & Cryogenics, Advanced Science Research Center, Okayama University for the ICP-OES measurements.
Funding Information:
The authors thank Addis Ababa University Thematic Research Fund for supporting the project titled ?Developing Innovative Microfluidic Paper-Based Analytical Devices (?-PADs): Viable solution for Environmental Monitoring in Ethiopia? at the Center for Environmental Science. A. M. also acknowledges Wollo University and Okayama University for providing him with a Ph. D. study leave and with the opportunity of working for the Ph. D. study, respectively. The authors gratefully thank Division of Instrumental Analysis, Department of Instrumental Analysis & Cryogenics, Advanced Science Research Center, Okayama University for the ICP-OES measurements.
Publisher Copyright:
© 2021, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2021/5
Y1 - 2021/5
N2 - Speciation of chromium (Cr) was demonstrated using microfluidic paper-based analytical devices (μ-PADs) that permit the colorimetric determination of hexavalent chromium (Cr(VI)) and trivalent chromium (Cr(III)) via online oxidation. The μ-PADs consist of left and right channels that allow the simultaneous measurements of Cr(VI) and total Cr based on the colorimetric reaction of Cr(VI) with 1,5-diphenylcarbazide (DPC). For the determination of Cr(VI), a sample solution was directly reacted with DPC in the left channels whereas total Cr was determined in the right channels, which permitted online oxidation in the pretreatment zone containing cerium (IV) (Ce(IV)) followed by a colorimetric reaction with DPC. We found that the online oxidation of Cr(III) proceeded 100% whereas Ce(IV) inhibited the reaction of Cr(VI) with DPC. Therefore, speciation can be achieved by measuring the Cr(VI) and total Cr in the left and right channels followed by the subtraction of Cr(VI) from total Cr. The limits of detection and quantification were 0.008 and 0.02 mg L−1 for Cr(VI) and 0.07 and 0.1 mg L−1 for Cr(III) or total Cr, respectively. The linear dynamic ranges were 0.02–100 mg L−1 and 0.1–60 mg L−1 for Cr(VI) and Cr(III), respectively. The RSDs were less than 7.5%. The results obtained using μ-PADs were in good agreement with those obtained via ICP-OES with recoveries of 92–108% for Cr(III) and 108–110% for Cr (VI) using μ-PADs, and 106–110% for total Cr using ICP-OES. Thus, the μ-PADs could potentially be utilized for the speciation of chromium in developing countries where environmental pollution and the availability of sophisticated instruments are significant problems.
AB - Speciation of chromium (Cr) was demonstrated using microfluidic paper-based analytical devices (μ-PADs) that permit the colorimetric determination of hexavalent chromium (Cr(VI)) and trivalent chromium (Cr(III)) via online oxidation. The μ-PADs consist of left and right channels that allow the simultaneous measurements of Cr(VI) and total Cr based on the colorimetric reaction of Cr(VI) with 1,5-diphenylcarbazide (DPC). For the determination of Cr(VI), a sample solution was directly reacted with DPC in the left channels whereas total Cr was determined in the right channels, which permitted online oxidation in the pretreatment zone containing cerium (IV) (Ce(IV)) followed by a colorimetric reaction with DPC. We found that the online oxidation of Cr(III) proceeded 100% whereas Ce(IV) inhibited the reaction of Cr(VI) with DPC. Therefore, speciation can be achieved by measuring the Cr(VI) and total Cr in the left and right channels followed by the subtraction of Cr(VI) from total Cr. The limits of detection and quantification were 0.008 and 0.02 mg L−1 for Cr(VI) and 0.07 and 0.1 mg L−1 for Cr(III) or total Cr, respectively. The linear dynamic ranges were 0.02–100 mg L−1 and 0.1–60 mg L−1 for Cr(VI) and Cr(III), respectively. The RSDs were less than 7.5%. The results obtained using μ-PADs were in good agreement with those obtained via ICP-OES with recoveries of 92–108% for Cr(III) and 108–110% for Cr (VI) using μ-PADs, and 106–110% for total Cr using ICP-OES. Thus, the μ-PADs could potentially be utilized for the speciation of chromium in developing countries where environmental pollution and the availability of sophisticated instruments are significant problems.
KW - Chromium
KW - Cr(III)
KW - Cr(VI)
KW - Microfluidic paper-based analytical device
KW - Online oxidation
KW - Speciation
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U2 - 10.1007/s00216-021-03274-y
DO - 10.1007/s00216-021-03274-y
M3 - Article
C2 - 33715041
AN - SCOPUS:85102712537
SN - 1618-2642
VL - 413
SP - 3339
EP - 3347
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 12
ER -