Speciation of chromium in water samples using microfluidic paper-based analytical devices with online oxidation of trivalent chromium.

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.

Adsorption enrichment integrated with paper-based devices for detection of trace levels of hexavalent chromium in water samples.

In the present study, a sensitive microfluidic paper-based analytical device (µ-PADs) integrated with adsorption enrichment procedure was developed to analyze Cr(VI) in water samples. The affecting factors, including pH and amounts of reagents were optimized. The limit of detection of 0.0015 mg L-1 and linear range of 0.005-2 mg L-1 were achieved with good intra- and inter-day precision of 5.1 and 7.6% RSD, respectively. The results obtained by the proposed method were validated by inductively coupled plasma-optical emission spectrometry (ICP-OES). The recoveries of the present method and ICP-OES were ranged from 96.3 to 109.0‬% and 106.0 to 109.7%, respectively. The two sets of (µ-PADs and ICP-OES) results were in a good agreement as paired t-test indicated no significant differences. The proposed method could be utilized for analyzing trace levels of Cr(VI) in water samples in the absence of conventional analytical instruments.

Microfluidic paper-based analytical devices coupled with coprecipitation enrichment show improved trace analysis of copper ions in water samples.

The present study focused on improving sensitivity to trace levels of Cu(II) by subjecting microfluidic paper-based analytical devices (µ-PADs) to a preconcentration process via coprecipitation using aluminum hydroxide. The experimental conditions were optimized for the pH of the coprecipitation, centrifugation, and amounts of reagents that were deposited onto µ-PADs for the Cu(II) assay. The resultant limit of detection reached as low as 0.003 mg L-1 with a linear range of 0.01-2.00 mg L-1. The relative standard deviations for intra- and inter-day precision were 3.2 and 4.6%, respectively (n = 9). Spiked water samples were analyzed using the µ-PADs after coprecipitation preconcentration. The results were verified by comparing them with those of inductively coupled plasma-optical emission spectrometry (ICP-OES). Recoveries ranged from 97.1 to 104% and from 98.7 to 105% using the present method and ICP-OES, respectively. These results suggest that the simple, highly sensitive, and inexpensive proposed method would be helpful for analyzing trace levels of Cu(II) in water samples in poorly equipped laboratories.

Remote Investigation of Total Chromium Determination in Environmental Samples of the Kombolcha Industrial Zone, Ethiopia, Using Microfluidic Paper-based Analytical Devices.

Microfluidic paper-based analytical devices (µ-PADs) fabricated in Japan were employed for the determination of total chromium (Cr) in water, soil, and lettuce irrigated with wastewater in Ethiopia. The µ-PADs, which were printed by wax printing in Japan, were transported to Ethiopia and prepared for the determination of total Cr by adding appropriate reagents to the pretreatment and detection zones. Soil and lettuce samples were determined by the µ-PADs and a UV-Vis spectrophotometer in Ethiopia. A paired t-test showed that the mean total Cr concentrations determined in the soil and lettuce samples were not significantly different between µ-PADs and UV-Vis spectrophotometric analysis at the 5% level of significance. This implies that the µ-PADs have good accuracy and reliability, and could be employed to monitor Cr in environmental samples. We found that the total Cr concentrations in all soil and lettuce samples were above the permissible limit. Moreover, evaluating Cr contamination level using the geo-accumulation index indicated that the soils were contaminated with Cr moderately to heavily. Thus, the present work successfully demonstrated the potential of remote investigations of pollution in a less-equipped laboratory by transporting the µ-PADs fabricated in another laboratory.