It is a big challenge to apply laser induced breakdown spectroscopy (LIBS) to ocean in situ detection, but there are ample opportunities for LIBS development too. In the present work, laboratory investigations of LIBS on natural seawater at different pressures from 0.1 to 40 MPa were carried out. Pressure and laser pulse energy effects on LIBS emission were investigated. The result showed that enhanced LIBS emission can be obtained under elevated ambient pressure conditions. The line broadening of lines increases as a function of pressure. The time resolved LIBS emission results demonstrated that plasma emission is weakly dependent on the ambient pressure during the early stage of plasma and the pressure has a significant influence on the plasma form during plasma evaluation at a later stage of plasma. The obtained results suggested that the LIBS technique has the potential to be developed as an in situ chemical sensing technique for ocean applications.

In recent years, the investigation and exploitation of hydrothermal region and polymetallic mineral areas has become a hot topic. The emergence of underwater vehicle platforms has made it possible for new chemical sensors to be applied in marine in-situ detection. Laser-induced breakdown spectroscopy (LIBS), with its advantages of rapid real-time analysis, sampling without pretreatment, simultaneous multi-element detection and stand-off detection, has great potential in marine applications. In this paper, a newly more compact and lighter underwater LIBS system based on the LIBSea system named LIBSea II was developed and tested both in the laboratory and sea trials. The system consists of a Nd:YAG single-pulse laser at 1064 nm, a fiber spectrometer, optical layout, a power supply module and an internal environment sensor. The system is encapsulated in a pressure vessel (Φ 190 mm × L 588 mm) with an optical window on the end cap. Experimental parameters of the system including laser energy and delay time were firstly optimized in the laboratory. Then, field test of the system in nearshore was performed with various samples, including pure metal and alloy samples as well as a manganese nodule sample from deep sea, to verify the detection performance of the LIBSea II system. In 2019, the system was deployed on a remotely operated vehicle (ROV) of Haima for deep sea trial, and atomic lines of K, Na, Ca and strong molecular bands of CaOH from a carbonate rock sample were obtained for the first time at depths of 1400 m. These results show that the LIBSea II system has great potential to be used in deep-sea geological exploration.

A normalization method for underwater LIBS signals by using a synchronous plasma image is proposed and used for quantitative analysis.

In this study, an ultrasonic nebulizer unit was established to improve the quantitative analysis ability of laser-induced breakdown spectroscopy (LIBS) for liquid samples detection, using solutions of the heavy metal element Pb as an example. An analytical procedure was designed to guarantee the stability and repeatability of the LIBS signal. A series of experiments were carried out strictly according to the procedure. The experimental parameters were optimized based on studies of the pulse energy influence and temporal evolution of the emission features. The plasma temperature and electron density were calculated to confirm the LTE state of the plasma. Normalizing the intensities by background was demonstrated to be an appropriate method in this work. The linear range of this system for Pb analysis was confirmed over a concentration range of 0–4,150ppm by measuring 12 samples with different concentrations. The correlation coefficient of the fitted calibration curve was as high as 99.94% in the linear range, and the LOD of Pb was confirmed as 2.93ppm. Concentration prediction experiments were performed on a further six samples. The excellent quantitative ability of the system was demonstrated by comparison of the real and predicted concentrations of the samples. The lowest relative error was 0.043% and the highest was no more than 7.1%.

The detection of manganese (Mn) in industrial wastewater and seawater plays an important role in pollution monitoring and the investigation of geochemical and biological processes in the ocean. An approach has been introduced in this work to improve the detection sensitivity of Mn in liquids by laser-induced breakdown spectroscopy with a filter paper as solid substrate. The calibration curves of Mn in aqueous solutions were obtained with the detection of a Czerny–Turner spectrometer and an echelle spectrometer, respectively. The results showed that the Czerny–Turner spectrometer equipped with an intensified charge-coupled device (ICCD) had a more sensitive detection of Mn in aqueous solution with this approach. The limit of detection (LOD) for Mn was down to 0.11 mg/L with laser pulse energy of 90 mJ. With the same approach, the compact echelle spectrometer equipped with an ICCD was used to verify the feasibility for rapid onsite detection. The calibration curves for Mn in simulated industrial wastewater and seawater were constructed to calculate relevant LODs. The LODs of Mn were 2.78 mg/L in mixed solutions and 2.73 mg/L in seawater by calculation. Both the calibration curves and LODs were affected slightly by the matrix effect in the experiment. In order to assess the accuracy, a mixed solution including Mn, Cr, Cd, and Cu with known concentrations was determined, and good agreement between the measured and real values were achieved. It demonstrated that this approach has significant potential for rapid onsite detection of Mn and other metal elements in industrial wastewater and seawater.

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