Evaluation of lignin and dip coating for elemental analysis by thin film microextraction followed by laser-induced breakdown spectroscopy

Separation and preconcentration procedures are often necessary to eliminate interferents, enhance sensitivity, and improve detection limits. Conventional solid-phase extraction (batch) finds extensive applications in the determination of various analytes, particularly in low concentrations and complex matrices such as environmental, food, and biological samples. However, drawbacks include high reagent consumption, time-consuming sample processing and low analytical throughput. To address these issues and promote Green Analytical Chemistry (GAC), novel methods have emerged, with solid-phase and liquid-phase microextraction being notable examples. Thin Film Microextraction (TFME) represents an innovative approach involving a solid support coated with a thin layer of adsorbent material, attached to a rod and immersed in the sample solution. Extracted analytes can be quantified either after desorption (elution) or directly on the thin film. This article aims to explore TFME's potential when combined with Laser-Induced Breakdown Spectroscopy (LIBS) for Cd, Cr and Ni determination using lignin as adsorbent material deposited on a solid substrate by dip coating. Under optimized conditions, limits of detection obtained were 1.76 μg kg⁻¹ (Cd), 5.72 μg kg⁻¹ (Cr), and 3.27 μg kg⁻¹ (Ni). The accuracy of the proposed method was evaluated through the analysis of a certified reference material (ERM® CA713), drinking and tap water.