Group of Applied Instrumental Analysis, Department of Chemistry, Federal University of São Carlos, São Carlos, São Paulo State, 13565-905, Brazil.
Group of Applied Instrumental Analysis, Department of Chemistry, Federal University of São Carlos, São Carlos, São Paulo State, 13565-905, Brazil.
Anal Chim Acta. 2019 Jul 11;1061:42-49. doi: 10.1016/j.aca.2019.02.038. Epub 2019 Mar 4.
Mobile phones are one of the fastest growing types of electronic waste disposed of world-wide. One of the main components in these devices is the LCD (liquid crystal display) panel that contains conductive electrodes made of indium tin oxide. A large amount of In, which is categorized as a critical raw element, has been used to manufacture indium tin oxide films. This study applies laser-induced breakdown spectroscopy (LIBS) for the analysis of LCD samples from mobile phones in order to determine the In content. Both conventional univariate calibration and non-traditional calibration using different transition energies (emission lines), named multi-energy calibration (MEC), were assessed. To evaluate the accuracy of the results, Method EPA 3052 was performed for acid digestion of the samples using microwave-assistance, and the In content was determined by ICP OES. Indium concentrations ranged from 35 to 47 mg kg for all samples evaluated. The results showed the best accuracy for LIBS methods after the spectra were normalized by the carbon line at 193.09 nm. The univariate-LIBS model showed a standard error of calibration (SEC) about 10-fold lower than the samples' concentration, LOD and LOQ of 0.3 and 1.0 mg kg, respectively. MEC proved to be a fast and efficient alternative for direct solid analysis, and In concentrations were determined by LIBS using only two calibration pellets. The LOD and LOQ for MEC-LIBS method were 2.1 and 7 mg kg, respectively.
手机是全球范围内增长最快的电子废物类型之一。这些设备的主要部件之一是含有氧化铟锡(ITO)导电电极的液晶(LCD)显示屏。大量的铟被用于制造 ITO 薄膜,而铟被归类为关键原材料。本研究应用激光诱导击穿光谱(LIBS)分析手机的 LCD 样品,以确定铟的含量。评估了传统的单变量校准和使用不同跃迁能量(发射线)的非传统校准,称为多能量校准(MEC)。为了评估结果的准确性,使用微波辅助酸消解对样品进行了 EPA 3052 方法,并通过 ICP-OES 测定铟的含量。所有评估的样品中,铟的浓度范围为 35 至 47mgkg。结果表明,在对光谱进行归一化处理后,LIBS 方法的准确度最高,其中碳线在 193.09nm 处归一化。单变量 LIBS 模型的校准标准误差(SEC)比样品浓度低约 10 倍,LOD 和 LOQ 分别为 0.3 和 1.0mgkg。MEC 被证明是一种快速有效的直接固体分析替代方法,只需使用两个校准丸即可通过 LIBS 测定铟浓度。MEC-LIBS 方法的 LOD 和 LOQ 分别为 2.1 和 7mgkg。