Evaluation of Thin Film Microextraction for trace elemental analysis of liquid samples using LIBS detection

An analytical methodology based in the combination of Thin Film Microextraction with Laser-induced Breakdown Spectroscopy (TFME-LIBS) was investigated, for the first time, for detection of Cu, Cr, Ni and Pb in aqueous solutions. In this methodology, the analytes were extracted in a thin film of adsorbent material deposited on a solid support, which was introduced in the sample to analyse. After extraction, the analytes retained in the adsorbent were analysed by LIBS. In order to obtain adsorbent films useful for the microextraction step, two different experimental procedures for film generation, denoted as Drop Casting Deposition and Mould Deposition, were evaluated. In both cases, graphene oxide was used as adsorbent material. The mould deposition procedure was found to produce more homogeneous graphene oxide layers, leading to more uniform distribution of the adsorbed analytes on the graphene oxide surface. Experimental parameters affecting the TFME procedure, such as the adsorbent amount and extraction time, were studied. Under optimum microextraction conditions, the analytical figures of merit of the proposed TFME-LIBS method were evaluated, leading to limits of detection ranging from 41 mu g kg(-1) and 52 mu g kg(-1). Method trueness, evaluated from the analysis of a real sample of bottle water, led to recovery values about 70%, indicating the existence of strong matrix effects probably due to the presence of major cations in the bottle water. After 50% dilution of the sample with deionized water, recoveries values improved to 100%-108%.

Automated summary

An analytical methodology combining Thin Film Microextraction with Laser-induced Breakdown Spectroscopy (TFME-LIBS) was investigated for the detection of Cu, Cr, Ni, and Pb in aqueous solutions. Experimental results showed that the use of the mould deposition procedure produced more uniform graphene oxide layers, leading to a more even distribution of the adsorbed analytes on the graphene oxide surface.