Search Results (216)

This study presents a comprehensive numerical simulation and thermal performance analysis of a novel modular floating solar still system, featuring integrated heat-pipe vacuum tube collectors, designed for seawater desalination. This innovative system—subject of International Patent Application WO 2023/062261 A1—not only aims to enhance efficiency and scalability beyond traditional solar stills, but also addresses the significant environmental challenge of concentrated brine discharge inherent in conventional desalination methods. The study evolved from an initial theoretical model to a rigorous dynamic thermal model, validated using real hourly meteorological data from Málaga, Andalusia, Spain. This modelling approach was developed to quantify heat transfer mechanisms and accurately predict system performance. The refined hourly simulation forecasts an annual freshwater production of approximately 174 L per unit. Notably, a preliminary economic assessment estimates the Cost of Produced Water per Litre (CPL) at 0.7509 EUR/litre, establishing a valuable baseline for future optimisation. These findings underscore the critical importance of dynamic hourly simulations for realistic performance prediction and validate the technical and preliminary economic feasibility of this novel approach. The system’s projected output, modular floating design, and significant environmental advantages position it as a promising and sustainable solution for freshwater production, particularly in coastal regions and sensitive marine ecosystems. This work provides a solid foundation for future experimental validation, cost optimisation, and scalable implementation of renewable energy-driven desalination. Full article

In order to improve energy utilization efficiency and the flexibility of resource transfer in oceanic-island-group microgrids, a water–electricity–hydrogen flexible scheduling strategy based on a multi-rate hydrogen-powered ship is proposed. First, the characteristics of the seawater desalination unit (SDU), proton exchange membrane electrolyzer (PEMEL), and battery system (BS) in consuming surplus renewable energy on resource islands are analyzed. The variable-efficiency operation characteristics of the SDU and PEMEL are established, and the effect of battery life loss is also taken into account. Second, a spatio-temporal model for the multi-rate hydrogen-powered ship is proposed to incorporate speed adjustment into the system optimization framework for flexible resource transfer among islands. Finally, with the goal of minimizing the total cost of the system, a flexible water–electricity–hydrogen hybrid resource transfer model is constructed, and a certain island group in the South China Sea is used as an example for simulation and analysis. The results show that the proposed scheduling strategy can effectively reduce energy loss, promote renewable energy absorption, and improve the flexibility of resource transfer. Full article

By adjusting NiCr target power, five CrNiBN coatings with different Ni contents were fabricated on 45 steel by magnetron sputtering with the aim of improving corrosion resistance of CrBN coatings in seawater. The structure and morphology of CrNiBN coatings were characterized by X-ray diffraction and scanning electron microscope, while its electrochemical properties were evaluated by open circuit potential, electrochemical impedance spectroscopy, and potential dynamic polarization. The results demonstrated that Ni incorporation could reduce the surface porosity of CrBN coatings from 16.8% to 7.7% as Ni content increased from 4.35 at% to 19.62 at%. On this basis, when Ni increased from 4.35 at% to 7.28 at%, self-corrosion potential gradually increased, which prompted the CrNiBN coating with 7.28 at% Ni to present the highest charge transfer resistance R_ct of 1.965 × 10⁴ Ω·cm² and the highest polarization resistance R_p of 74.9 kΩ·cm². However, more Ni doping from 12.54 at% to 19.62 at% would decrease self-corrosion potential and trigger oxidation. Consequently, the CrNiBN coatings with Ni content from 12.54 at% to 19.62 at% presented decreasing R_ct and R_p. Even so, the corrosion resistance of the CrNiBN coating was still better than that of CrBN coating indicating an improved corrosion inhibition efficiency by 12.53 times. Full article

The increasing demand for sustainable energy and clean water has prompted the exploration of alternative solutions to reduce reliance on fossil fuels. In this context, hydrogen production through water electrolysis powered by solar energy presents a promising pathway toward a zero-carbon footprint. This study investigates the potential of copper slag, an abundant industrial waste, as a low-cost electrocatalyst for the hydrogen evolution reaction (HER) in contact with saline water such as 0.5 M NaCl and seawater, comparing the electrochemical response when in contact with geothermal water from El Tatio (Atacama Desert). The physicochemical characterisation of copper slag was performed using XRD, Raman, and SEM-EDS to determine its surface properties. Electrochemical evaluations were conducted in 0.5 M NaCl and natural seawater using polarisation techniques to assess the corrosion behaviour and catalytic efficiency of the copper slag electrodes. The results indicate that copper slag exhibits high stability and promising HER kinetics, particularly in seawater, where its mesoporous structure facilitates efficient charge transfer processes. The key novelty of this manuscript lies in the direct revalorisation of untreated copper slag as a functional electrode for HER in real seawater and geothermal water, avoiding the use of expensive noble metals and aligning with circular economy principles. This innovative combination of recycled material and natural saline electrolyte enhances both the technical and economic viability of electrolysis, while reducing environmental impact and promoting green hydrogen production in coastal regions with high solar potential. This research contributes to the value of industrial waste, offering a viable pathway for advancing sustainable hydrogen technologies in real-world environments. Full article

Seawater electrolysis offers a sustainable route for large-scale, carbon-neutral hydrogen production, but its industrial application is limited by the poor efficiency and durability of current electrocatalysts under high current densities. Herein, we synthesized ultrasmall Pt nanoclusters uniformly anchored on FeCoNi phosphide nanosheet arrays, forming a composite catalyst with outstanding hydrogen evolution reaction (HER) performance in alkaline seawater. The catalyst achieves an ultralow overpotential of 17 mV at −10 mA cm⁻², far surpassing commercial Pt/C, and stably delivers industrial-level current densities up to 2000 A m⁻² for over 2400 h with minimal voltage degradation and low energy consumption (4.16 kWh/Nm³ H₂). X-ray photoelectron spectroscopy revealed strong interfacial electronic interactions between Pt and Fe/Co species, involving electron transfer from Pt that modulates its electronic structure, weakens hydrogen adsorption, and enhances both HER kinetics and Pt dispersion. This work presents a scalable and robust catalyst platform, bridging the gap between laboratory research and industrial seawater electrolysis for green hydrogen production. Full article

To achieve efficient prediction and optimization of the energy consumption of ship central cooling systems, this paper first constructed and validated a high-precision multi-physical domain simulation model of the ship central cooling system based on fluid heat transfer principles and the physical network method. Then, simulation experiments were designed using the Box–Behnken design (BBD) method to study the effects of five key parameters—main engine power, seawater temperature, seawater pump speed, low-temperature fresh water three-way valve opening, and low-temperature fresh water flow rate—on system energy consumption. Based on the simulation data, an energy consumption prediction model was constructed using response surface methodology (RSM). This prediction model exhibited excellent goodness of fit and prediction ability (coefficient of determination R² = 0.9688, adjusted R²_adj = 0.9438, predicted R²_pred = 0.8752), with a maximum relative error of only 1.2% compared to the simulation data, confirming its high accuracy. Sensitivity analysis based on this prediction model indicated that main engine power, seawater pump speed, seawater temperature, and three-way valve opening were the dominant single factors affecting energy consumption. Further analysis revealed a significant interaction between main engine power and seawater pump speed. This interaction resulted in non-linear changes in system energy consumption, which were particularly prominent under operating conditions such as high power. This study provides an accurate prediction model and theoretical guidance on the influence patterns of key parameters for the simulation-driven design, operational optimization, and energy saving of ship central cooling systems. Full article

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. Full article

This study systematically investigates for the first time the effects of dual-site co-cultivation on spectral characteristics and trace element enrichment in marine-cultured Akoya pearls from Beihai, China. Akoya pearls were cultured over a one-year period, with the final 40-day stage designated as the terminal phase. During this period, two experimental groups of pearl oysters were established: Group Y remained in Beihai for continued local cultivation and harvest, while Group B was transferred to Weihai, Shandong Province, for terminal-stage farming under different thermal conditions. A series of comparative analyses were performed using Fourier-transform infrared (FTIR) spectroscopy, ultraviolet-visible (UV-Vis) spectroscopy, Raman spectroscopy, X-ray fluorescence (XRF), and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The FTIR results revealed distinct differences between the two groups in the distribution of amide and polysaccharide functional groups, particularly around 1643 cm⁻¹ and 1100 cm⁻¹. The UV-Vis spectra of Group B displayed characteristic absorption bands at 430 nm and 460 nm, associated with the organic matrix of the nacre. Raman spectroscopy further indicated a higher abundance of organic-related vibrational features in Group B. Additionally, both XRF and LA-ICP-MS analyses consistently showed significant differences in the concentrations and distributions of trace elements, particularly copper (Cu), cobalt (Co), and zinc (Zn). The findings demonstrate that the dual-site co-cultivation mode significantly impacts both the organic composition and trace element enrichment patterns in seawater Akoya pearls. This research provides valuable references for optimizing environmental parameters in pearl cultivation processes. Full article

Composite materials have the advantages of high strength and low weight, and are therefore used in many areas. However, in humid and marine environments, mechanical properties may deteriorate due to moisture diffusion, especially in glass fiber reinforced polymers (GFRP) and carbon fiber reinforced polymers (CFRP). This study investigated the damage formation and changes in mechanical properties of single-layer adhesive-bonded GFRP and CFRP connections under the effect of sea water. In the experiment, 0/90 orientation, twill-woven GFRP (7 ply) and CFRP (8 ply) plates were produced as prepreg using the hand lay-up method in accordance with ASTM D5868-01 standard. CNC Router was used to cut 36 samples were cut from the plates produced for the experiments. The samples were kept in sea water taken from the Aegean Sea, at 3.3–3.7% salinity and 23.5 °C temperature, for 1, 2, 3, 6, and 15 months. Moisture absorption was monitored by periodic weighings; then, the connections were subjected to three-point bending tests according to the ASTM D790 standard. The damages were analyzed microscopically with SEM (ZEISS GEMINI SEM 560). As a result of 15 months of seawater storage, moisture absorption reached 4.83% in GFRP and 0.96% in CFRP. According to the three-point bending tests, the Young modulus of GFRP connections decreased by 25.23% compared to dry samples; this decrease was 11.13% in CFRP. Moisture diffusion and retention behavior were analyzed according to Fick’s laws, and the moisture transfer mechanism of single-lap adhesively bonded composites under the effect of seawater was evaluated. Full article

Using direct seawater electrolysis (DSE) for hydrogen production has garnered increasing scientific attention as a promising pathway toward sustainable energy solutions. Given the complex ionic environment of seawater, researchers have proposed a diverse range of strategies aimed at addressing the issue of enhancing the corrosion resistance of anodes, yet no optimal solution has been found so far. Among the emerging approaches, a design using multilayer electrode architecture offers notable advantages by introducing abundant active sites, diverse chemical environments, and robust physical structures. Crucially, these configurations enable the synergistic integration of distinct material properties across different layers, thereby enhancing both electrochemical activity and structural stability in harsh seawater environments. Despite these benefits, a limited understanding of the role played by solid–solid interfaces has hindered the rational design and practical application of such electrodes. This review focuses on the design principles and functional roles of solid–solid interfaces in multilayer anodes for the oxygen evolution reaction (OER) under DSE conditions. In addition, we systematically summarize and discuss the representative fabrication methods for constructing solid–solid interfaces in hierarchically structured electrodes. By screening recent advances in these techniques, we further highlight how engineered interfaces influence interfacial bonding, electron transfer, and mass transport during DSE processes, enhancing the intrinsic catalytic activity, as well as protecting the metallic electrode from corrosion. Finally, current challenges and future research directions to deepen the mechanistic understanding of interface phenomena are discussed, with the aim of accelerating the development of robust and scalable electrodes for direct seawater electrolysis. Full article

This work aims to characterize flow-accelerated corrosion of carbon steel A36 coupons exposed to simulated treated reverse-osmosis seawater under ambient conditions and a Reynolds number range of 6000 to 25,000 using a standard corrosion testing method. The flow behavior in the corrosion compartment and the turbulent parameters were determined by computational fluid dynamics simulation. Using selected flow parameters, complemented with experimental corrosion rate measurements, the oxygen mass transfer coefficients (m_c) and the rate constant for the cathodic reaction (k_c) at the coupon surface were determined. As expected, m_c depends only on the fluid conditions, while k_c is highly influenced by interface resistance, leading to significantly different runs with and without a corrosion inhibitor. The dissimilar fluid flow distribution on intrados and extrados generates irregular corrosion patterns, depending on the angular position of the coupon inside the corrosion compartment. Morphological studies using scanning electron microscopy and atomic force microscopy support simulation results. Full article

This study examines the use of a1 mm-diameter tubular microreactor submerged in a temperature-controlled water bath to activate potassium persulfate (KPS) via thermal, Fe²⁺-catalyzed, and combined thermo-catalytic processes for degrading the persistent textile dye Safranin O (SO). The efficiency of these methods was evaluated under varying conditions, including KPS, dye, and Fe^2⁺ flow rates, solution pH, reactor length, and water matrix quality (deionized water, tap water, seawater, and secondary effluent from a wastewater treatment plant (SEWWTP)) across bath temperatures of 30–80 °C. Total organic carbon (TOC) analysis validated the results. Maximum dye conversion (up to 89%) occurred at 70 °C, with no improvement beyond this temperature, mainly due to radical-radical recombination. Longer reactors (2–6 m) enhanced conversion, though this effect diminished at higher temperatures due to efficient thermal activation. Increasing dye flow rates reduced removal efficiency, particularly above 50 °C, highlighting kinetic and mass transfer limitations. Persulfate flow rate increases improved conversion, but a plateau emerged at 80 °C. At lower temperatures (30–40 °C), Fe²⁺ addition significantly boosted SO conversion in deionized water. Between 40 and 50 °C, conversion rose from 30.27% (0 mM Fe²⁺) to 85.91% (0.2 mM Fe²⁺) at 50 °C. At higher temperatures (60–80 °C), conversion peaked at 70 °C for lower Fe²⁺ concentrations (100% for 0.01–0.05 mM Fe²⁺), but higher Fe²⁺ levels (0.1–0.2 mM) caused a decline above 60 °C, dropping to 68.44% for 0.2 mM Fe²⁺ at 80 °C. Deionized, tap, and mineral water showed similar performance, while river water, secondary effluent, and seawater inhibited SO conversion at lower temperatures (30–60 °C). At 70–80 °C, all matrices achieved efficiencies comparable to deionized water for both thermal and thermo-catalytic activation. The thermo-catalytic system achieved >50% TOC reduction, indicating significant organic matter mineralization. The results were comprehensively analyzed in relation to thermal and kinetic factors influencing the performance of continuous-flow reactors. Full article

The periodate/hydrogen peroxide (PI/H₂O₂) system is a recently developed advanced oxidation process (AOP) characterized by its rapid reaction kinetics, making it highly suitable for continuous-flow applications compared to conventional batch systems. Despite its potential, no prior studies have investigated its performance under flowing conditions. This work presents the first application of the PI/H₂O₂ process in a tubular microreactor, a promising technology for enhancing mass transfer and process efficiency. The degradation of textile dyes (specifically Basic Yellow 28 (BY28)) was systematically evaluated under various operating conditions, including reactant concentrations, flow rates, reactor length, and temperature. The results demonstrated that higher H₂O₂ flow rates, increased PI dosages, and moderate dye concentrations (25 µM) significantly improved degradation efficiency, achieving complete mineralization at 2 mM PI and H₂O₂ flow rates of 80–120 µL/s. Conversely, elevated temperatures negatively impacted the process performance. The influence of organic and inorganic constituents was also examined, revealing that surfactants (SDS, Triton X-100, Tween 20, and Tween 80) and organic compounds (sucrose and glucose) acted as strong hydroxyl radical scavengers, substantially inhibiting dye oxidation—particularly at higher concentrations, where nearly complete suppression was observed. Furthermore, the impact of water quality was assessed using different real matrices, including tap water, seawater, river water, and secondary effluents from a municipal wastewater treatment plant (SEWWTP). While tap water exhibited minimal inhibition, river water and SEWWTP significantly reduced process efficiency due to their high organic content competing with reactive oxygen species (ROS). Despite its high salt content, seawater remained a viable medium for dye degradation, suggesting that further optimization could enhance process performance in saline environments. Overall, this study highlights the feasibility of the PI/H₂O₂ process in continuous-flow microreactors and underscores the importance of considering competing organic and inorganic constituents in real wastewater applications. The findings provide valuable insights for optimizing AOPs in industrial and municipal wastewater treatment systems. Full article

The ballast tank is a critical system for LNG carriers, ensuring structural safety and stability during navigation. When LNG carriers navigate in polar regions, the ballast tank is prone to freezing, which will reduce the efficiency of ballast water circulation. Furthermore, the freezing process generates frost heaving forces that may damage the walls of the ballast tank, shorten the structure’s service life, and disrupt the ship’s normal operations. Therefore, analyzing the freezing process of ballast tanks is essential. This paper focuses on the ballast tank of a polar LNG carrier as the research subject. It assumes that the ballast water is fresh water with unchanging physical properties and takes into account the environmental conditions in polar regions. A numerical simulation model of the freezing process within the ballast tank is established. This study investigates the influence of various environmental parameters on the freezing process and determines the evolution of ice shape in relation to temperature field changes under different environmental conditions. The results indicate that as the ambient temperature decreases, the rate of temperature reduction at the ballast water level accelerates, resulting in a thicker ice layer formed by freezing. Additionally, as the seawater temperature decreases, the rate of temperature decline in the ballast water at the bulkhead is significantly accelerated, leading to an increased rate of ice shape evolution. Furthermore, a reduction in the height of the ballast water level enhances the heat transfer rate of the ballast water, which markedly increases the degree of freezing in the ballast water. Full article

Penaeus monodon (black tiger shrimp) is one of the important shrimp species in aquaculture. Cryopreserving its sperm not only provides technical support for breeding but also effectively prevents the decline of genetic resources, promoting the sustainable development of its aquaculture industry. This study screened different types of diluents, cryoprotectants, and concentrations and explored equilibration time, cooling protocols, and thawing conditions, ultimately determining the optimal cryopreservation protocol for P. monodon sperm. The results showed that the optimal cryopreservation protocol involved using natural seawater as the diluent with 10% dimethyl sulfoxide (DMSO) as the cryoprotectant, in which the sperm suspension and cryoprotectant were mixed at a 1:1 (v/v) ratio and equilibrated at 4 °C for 30 min. Subsequently, cooling was performed using a programmable controlled-rate freezer: the temperature was reduced to −20 °C at −5 °C/min and held for 5 min; then cooled to −80 °C at −10 °C/min and held for 5 min; finally, the temperature was reduced to −180 °C at −20 °C/min. After cooling, the sperm samples were transferred to liquid nitrogen for long-term storage. The results demonstrated that thawing in a 37 °C water bath achieved the highest sperm motility compared to conditions at 27 °C, 32 °C, 42 °C, and 60 °C. After 15 days of liquid nitrogen storage, the sperm survival rate was 53.33 ± 9.18%. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) observations revealed that the sperm structure was intact before freezing, with a rounded head, a distinct acrosomal spike anterior to the head, a concentrated nucleus in the head, dense chromatin, and a smooth cell membrane surface. However, after freezing and thawing, the acrosomal spikes of some sperm were fractured, and the membrane structure was damaged. Enzyme activity analysis showed that during liquid nitrogen storage from 0 to 15 days, the enzyme activity of alkaline phosphatase (AKP) and acid phosphatase (ACP) in sperm gradually increased with significant differences observed compared to day 0 (p < 0.05). The activity of malondialdehyde (MDA) showed a gradual increase at 0, 5, and 10 days, but then decreased at day 15. The enzyme activity of catalase (CAT) showed no significant changes from 0 to 10 days (p > 0.05) but significantly increased on day 15 (p < 0.05). The activity of total superoxide dismutase (T-SOD) showed no significant changes from 0 to 5 days (p > 0.05) but significantly increased from days 10 to 15 (p < 0.05). These findings provide valuable insights into the cryopreservation of P. monodon sperm and will guide the optimization of cryoprotectant combinations and freezing protocols aimed at improving sperm survival rates. Full article