An experiment to investigate the potential of a laser-induced plasma method for determining concrete compressive strength was conducted by focusing a Nd:YAG laser on concrete samples with different degrees of compressive strength. This technique was developed in light of the role of the shock wave in the generation of a laser-induced plasma. It was found that the speed of the shock front depends on the hardness of the sample. It was also found that a positive relationship exists between the speed of the shock front and the ionization rate of the ablated atoms. Hence, the ratio of the intensity between the Ca(II) 396.8 nm and Ca(I) 422.6 nm emission lines detected from the laser-induced plasma can be used to examine the hardness of the material. In fact, it was observed that the ratio changes with respect to the change in the concrete compressive strength. The findings also show that the ratio increases with time after the cement is mixed with water.

Taking advantage of the differences between the interactions of transversely excited atmospheric (TEA) CO₂ lasers with metal and with organic powder, a new technique for the direct analysis of food powder samples has been developed. In this technique, the powder samples were placed into a small hole with a diameter of 2 mm and a depth of 3 mm and covered by a metal mesh. The TEA CO₂ laser (1500 mJ, 200 ns) was focused on the powder sample surfaces, passing through the metal mesh, at atmospheric pressure in nitrogen gas. It is hypothesized that the small hole functions to confine the powder particles and suppresses the blowing-off of sample, while the metal mesh works as the source of electrons to initiate the strong gas breakdown plasma. The confined powder particles are then ablated by laser irradiation and the ablated particles move into the strong gas breakdown plasma region to be atomized and excited; this method cannot be applied for the case of Nd:YAG lasers because in such case the metal mesh itself was ablated by the laser irradiation. A quantitative analysis of a milk powder sample containing different concentrations of Ca was successfully demonstrated, resulting in a good linear calibration curve with high precision.

It has been demonstrated that a spectrochemical analysis of carbon using the laser plasma method can be successfully applied to inspect the carbonation of concrete by detecting carbon produced in aged concrete by a chemical reaction of Ca(OH) ₂ with CO ₂ gas in environmental air, turning into CaCO ₃ , which induces degradation of the quality of building concrete. A comparative study has been made using a TEA CO ₂ laser (500–1000 mJ) and a Q-switched Nd– YAG laser (50–200 mJ) to search for the optimum conditions for carbon analysis, proving the advantage of the TEA CO ₂ laser for this purpose. Also, it was clarified that laser irradiation with suitable defocusing conditions is a crucial point for obtaining high sensitivity in the detection of carbon. Practical experiments on the inspection of carbonation were carried out using both a concrete sample that had been intentionally carbonated by exposure to high concentrations of CO ₂ gas and a naturally carbonated concrete sample. As a result, good coincidence was observed between the laser method and the ordinary method, which uses the chemical indicator phenolphthalein, implying that this laser technique is applicable as an in situ quantitative method of inspection for carbonation of concrete.

An experiment was carried out to demonstrate the detection of a hydrogen emission line, $\mathrm{H}\mathrm{I}656.2\mathrm{nm}$ $\left({\mathrm{H}}_{\alpha }\right)$ , in a plasma induced by a $\mathrm{Q}$ -switched $\mathrm{Nd-YAG}$ (YAG, yttrium aluminium garnet) laser in a low pressure gas on various types of samples, such as zinc, a glass slide, and a zircalloy tube. Contribution by surface water could be suppressed by a laser cleaning treatment and the resulting calibration curve obtained for zircalloy tube samples doped with various concentrations of hydrogen ($0$ , $200$ , $540$ , and $960$ ) suggest potential applications to the quantitative analysis of hydrogen. A study of the dynamic process represented by the time profiles of the hydrogen emission, in comparison with those for zinc atomic emission, revealed a specific feature that is related to the small mass of hydrogen. This specific feature can be explained by the shock wave excitation mechanism in terms of new hypothetical process, namely, a mismatch between the movement of ablated hydrogen atoms and the formation of the shock wave.