Meelapsom Rattapol, Jarujamrus Purim, Amatatongchai Maliwan, Chairam Sanoe, Kulsing Chadin, Shen Wei
Department of Chemistry and Center of Excellent for Innovation in Chemistry, Faculty of Science, Ubon Ratchathani University, Ubon Ratchathani 34190, Thailand.
Department of Chemistry and Center of Excellent for Innovation in Chemistry, Faculty of Science, Ubon Ratchathani University, Ubon Ratchathani 34190, Thailand.
Talanta. 2016 Aug 1;155:193-201. doi: 10.1016/j.talanta.2016.04.037. Epub 2016 Apr 21.
This study demonstrates chromatic analysis based on a simple red green blue (RGB) color model for sensitive and selective determination of mercury(II). The analysis was performed by monitoring the color change of a microfluidic Paper-based Analytical Device (µPAD). The device was fabricated by using alkyl ketene dimer (AKD)-inkjet printing and doped with unmodified silver nanoparticles (AgNPs) which were disintegrated when being exposed to mercury(II). The color intensity was detected by using an apparatus consisting of a digital camera and a homemade light box generating constant light intensity. A progressive increase in color intensity of the tested area on the µPAD (3.0mm) was observed with increasing mercury(II) concentration. The developed system enabled quantification of mercury(II) at low concentration with the detection limit of 0.001mgL(-1) (3 SD blank/slope of the calibration curve) and small sample volume uptake (2µL). The linearity range of the calibration curve in this technique was demonstrated from 0.05 to 7mgL(-1) (r(2)=0.998) with good precision (RSD less than 4.1%). Greater selectivity towards mercury(II) compared with potential interference ions was also observed. Furthermore, the percentage recoveries of spiked water samples were in an acceptable range which was in agreement with the values obtained from the conventional method utilizing cold vapor atomic absorption spectrometer (CVAAS). The proposed technique allows a rapid, simple, sensitive and selective analysis of trace mercury(II) in water samples.
本研究展示了基于简单红绿蓝(RGB)颜色模型的色度分析方法,用于灵敏且选择性地测定汞(II)。该分析通过监测微流控纸质分析装置(µPAD)的颜色变化来进行。该装置采用烷基烯酮二聚体(AKD)喷墨打印制造,并掺杂了未改性的银纳米颗粒(AgNPs),这些银纳米颗粒在暴露于汞(II)时会分解。使用由数码相机和自制的产生恒定光强的灯箱组成的仪器检测颜色强度。随着汞(II)浓度的增加,观察到µPAD上测试区域(3.0mm)的颜色强度逐渐增加。所开发的系统能够对低浓度汞(II)进行定量,检测限为0.001mgL⁻¹(3倍空白标准偏差/校准曲线斜率),且进样量小(2µL)。该技术校准曲线的线性范围为0.05至7mgL⁻¹(r² = 0.998),精密度良好(相对标准偏差小于4.1%)。与潜在干扰离子相比,对汞(II)也具有更高的选择性。此外,加标水样的回收率百分比在可接受范围内,与使用冷蒸气原子吸收光谱仪(CVAAS)的传统方法获得的值一致。所提出的技术能够对水样中的痕量汞(II)进行快速、简单、灵敏且选择性的分析。