The use of polymeric material in heavy metal removal from wastewater is trending. Heavy metal removal from wastewater of the industrial process is of utmost importance in green/sustainable manufacturing. Production of absorbent materials from a natural source for industrial wastewater has been on the increase. In this research, polyurethane foam (PUF), an adsorbent used by industries to adsorb heavy metal from wastewater, was prepared from a renewable source. Castor oil-based polyurethane foam (COPUF) was produced and modified for improved adsorption performance using fillers, analyzed with laser-induced breakdown spectroscopy (LIBS). The fillers (zeolite, bentonite, and activated carbon) were added to the COPUF matrix allowing the modification on its surface morphology and charge. The materials were characterized using Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), and thermal gravimetry analysis (TGA), while their adsorption performance was studied by comparing the LIBS spectra. The bentonite-modified COPUF (B/COPUF) gave the highest value of the normalized Pb I (405.7 nm) line intensity (2.3), followed by zeolite-modified COPUF (Z/COPUF) (1.9), and activated carbon-modified COPUF (AC/COPUF) (0.2), which indicates the adsorption performance of Pb²⁺ on the respective materials. The heavy metal ions’ adsorption on the B/COPUF dominantly resulted from the electrostatic attraction. This study demonstrated the potential use of B/COPUF in adsorption and LIBS quantitative analysis of aqueous heavy metal ions.

Global pollution from toxic metal waste has resulted in increased research on toxic metal adsorption. A cellulose acetate–polyurethane (CA–PU) film adsorbent was successfully prepared in this research. The cellulose acetate–polyurethane film adsorbent was prepared with a polycondensation reaction between cellulose acetate and methylene diphenyl diisocyanate. The CA–PU bond formation was confirmed by functional group analysis obtained from Fourier transform infrared (FTIR) spectroscopy. The obtained film was characterized for improved tensile and thermal properties with the addition of methylene diphenyl diisocyanate (MDI). The adsorption ability of the obtained film was evaluated with laser-induced breakdown spectroscopy (LIBS). The best film adsorbent from the LIBS was selected and studied for adsorption isotherm. The FTIR analysis confirmed the formation of the CA–PU bond from the polycondensation between cellulose acetate and the methylene diphenyl diisocyanate. The result showed that the addition of methylene diphenyl diisocyanate (MDI) resulted in the urethane network’s growth. The characterization result showed an improvement in the morphology, thermal stability, and tensile strength of the film. The LIBS studies showed improvement in the adsorption of Pb²⁺ with CA–PU compared with the neat CA. The isotherm studies revealed that Pb²⁺ adsorption by cellulose acetate–polyurethane film adsorbent was heterogeneously dependent on the Freundlich isotherm model (R² = 0.97044). Overall, the polycondensation method proposed by this study enhanced the Pb²⁺ removal, and was comparable to those reported in previous studies.

Hydrogen emission has been studied in laser plasma by focusing a Nd-YAG laser (1,064 nm, 50 mJ, 8 ns) on various types of samples, such as copper plate, zinc plate and glass plate. Several parameters influencing the emission were varied, such as the type of gas (air, nitrogen and helium), gas pressures (ranging from 2 up to 760 Torr) and laser power density. It was found that H_α emission with a narrow spectral width occurs with high efficiency when the laser plasma is produced in the low-pressure region. It was also confirmed that the conventional well-known laser-induced breakdown spectroscopy (LIBS), which usually carried out at atmospheric air pressure, cannot be applied for the analysis of hydrogen as impurity. This specific characteristic of the pressure dependence of hydrogen is interpreted based on our shock wave model, taking account of the fact that the hydrogen mass is extremely light compared to that of the host elements.