The diffusible hydrogen in steel weldments is one of the main reasons that led to hydrogen assisted cracking. In this paper, the results of literatures survey and preliminary tests of the diffusible hydrogen in underwater wet welding joint were presented. A fluid-discharge method of for measuring the diffusible hydrogen in weldment was introduced in detail. Two kinds of underwater welding electrode diffusible hydrogen are 26.5 mL/100g and 35.5 mL/100g by fluid-discharge method, which are high levels. The diffusible hydrogen of underwater welding is higher than atmospheric welding, and the result is closely related to welding material. The best way to control the diffusible hydrogen is adjusting welding material and improving fluidity of slag.

Utilizing renewable energy for green hydrogen production via electrolyzed seawater is a promising technology for the future. However, undesired chlorine evolution and the corrosive nature of seawater are crucial challenges for direct seawater splitting technology. In this work, heterojunctions of CoS₂/FeS₂ encapsulated in N-doped carbon nanocubes (denoted as CoS₂/FeS₂@NC) were designed by proposing the synchronous pyrolysis and vulcanization of polydopamine-coated coordination polymers. Such a synthetic strategy was demonstrated to be effective in increasing the favorable exposure of active sites, moderately regulating electronic structure, and remarkably facilitating charge transfer due to the controllable generation of unique core–shell structures with suitable carbon shells, leading to the excellent bifunctional electrocatalytic performance and enhanced stability of electrocatalysts. As a result, CoS₂/FeS₂@NC can be revealed as a superior water splitting catalyst, possessing a small voltage of 1.75 V and requiring 100.0 mA cm⁻² in 1 M KOH alkaline solution and 1.80 V for alkaline seawater media, with satisfactory long-term stability. This work presents fresh strategies for designing core–shell heterostructures and developing green technology for hydrogen production.

Phosphorus is a key indicator for water quality management due to its role in eutrophication. The variety of phosphorus-containing substances necessitates highly sensitive detection of total phosphorus, particularly through automated methods, to ensure water safety. This study involved the independent development of a sensor featuring an automated in situ detection technique. Utilizing potassium persulfate high-temperature oxidation and phosphorus molybdenum blue spectrophotometry, total phosphorus was monitored in situ via sequential injection technology. Additionally, the detection process and reaction conditions of the sensor were optimized, and a temperature compensation algorithm and turbidity correction were applied to mitigate environmental factors. Under optimal conditions, the sensor demonstrated a detection limit of 1.9 µg/L with a range of 6.5–1000 µg/L in seawater, and 1.2 µg/L with a range of 4.1–2000 µg/L in freshwater. The digestion efficiency for five representative phosphorus-containing substances was found to range from 87.3% ± 1.7% to 103.1% ± 0.6%. Notably, the sensor was deployed for in situ operation at a marine experimental station and online at a river monitoring station. With its integration, low power consumption, and high precision, the sensor enabled long-term unattended monitoring, delivering accurate, stable, and reliable results.