Direct determination of Al and Pb in waste printed circuit boards (PCB) by laser-induced breakdown spectroscopy (LIBS): Evaluation of calibration strategies and economic - environmental questions.

Matrix-matching calibration (MMC), two-point calibration transfer (TP CT), one-point and multi-line calibration (OP MLC), single-sample calibration (SSC) and calibration free (CF) were evaluated in order to overcome matrix effects in laser-induced breakdown spectroscopy (LIBS). These calibration strategies were evaluated for direct determination of Al and Pb in waste printed circuit boards (PCB) using direct solids analysis by LIBS. Each strategy has limitations and advantages of its implementation, for the correction of matrix effects, so that it allows elementary determination with adequate accuracy. The MMC and CF proved to be excellent calibration strategies for the determination of strategic (Al) and toxic (Pb) elements by LIBS, with good recoveries (ranging from 80-120%) and low relative standard deviation (RSD%) values. A detailed discussion of the advantages and limitations of each of these five calibration strategies evaluated for LIBS is presented in this study. Lead concentrations in waste PCB samples are 5-12 times higher than established by Directive 2011/65/EU, and the samples analyzed contain between 3 and 55 g kg-1 Al, being an interesting economic and recycling source for this metal.

Multiple response optimization of laser-induced breakdown spectroscopy parameters for multi-element analysis of soil samples.

Laser-induced breakdown spectroscopy (LIBS) is an emerging analytical technique to perform elemental analysis in natural samples independent of their physical state (solid, liquid, or gaseous). Due to its instrumental features, LIBS shows promising potential to perform analysis in situ and in environments at risk. Since the analytical performance of LIBS strongly depends on the choice of experimental conditions, each particular application needs a specific instrumental adjustment. The present study evaluated three LIBS instrumental parameters regarding their influences on signal-to-noise ratio (SNR) of seven elements in soil samples: laser pulse energy, delay time, and integration time gate. A multivariate technique was used due to the significant interaction among the evaluated parameters. Subsequently, to optimize LIBS parameters for each individual element response, a method for multiple response optimization was used. With only one simple screening design, it was possible to obtain a good combination among the studied parameters in order to simultaneously increase the SNR for all analytes. Moreover, the analysis of individual response for elements is helpful to understand their physical behavior in the plasma and also how they are embedded in the sample matrix.

Removal of chromium (III) by using coal as adsorbent.

The adsorption of Cr(III) by two different coal varieties from Lakhra and Thar coalfields (Pakistan) have been studied in batch mode. The effect of adsorbent dose, pH, contact time and agitation speed on the adsorption of Cr(III) by both the coals were investigated. Adsorption equilibrium was achieved in 40-50 min. The Langmuir, Freundlich and Temkin adsorption isotherms were used to elucidate the observed sorption phenomena. The maximum Cr(III) removal was 2.61 mg of Cr(III) per gram of LC (Lakhra coal) and 2.55 mg of Cr(III) per gram of TC (Thar coal) as evaluated from Langmuir isotherm. The heat of sorption was in the range 3.75-3.87 kJ/mol as evaluated from Temkin isotherm. Best results were obtained at pH>5. It is proposed that low rank coals of Pakistan can be used for removal of toxic metals like Cr(III) from industrial effluents/waste waters.

Laser-induced breakdown spectroscopy for quantitative spectrochemical analysis of geological materials: effects of the matrix and simultaneous determination.

A microscopic laser-induced breakdown spectrometer was used to evaluate the analytical matrix effect commonly observed in the analysis of geological materials. Samples were analyzed in either the powder or pressed pellet forms. Calibration curves of a number of iron and aluminum compounds showed a linear relationship between the elemental concentration and peak intensity. A direct determination of elemental content can thus be made from extrapolation on these calibration curves. To investigate matrix effects, synthetic model samples were prepared from various iron and aluminum compounds spiked with SiO2 and CaCO3. The addition of these matrices had a pronounced analytical effect on those compounds prepared as pressed pellets. However, results indicated the absence of matrix effects when the samples were presented to the laser as loose powders on tape and results were compared to certified values, indicating the reliability of this approach for accurate analysis, provided the sample particle diameters are greater than approximately 100 microm. Finally, the simultaneous analysis of two different elements was demonstrated using powders on tape.