Water Desalination Technique Research Articles

Recent Advances on Geothermal Integrated Water Desalination Techniques and Its Comparison with Other Renewable Resources

Solar radiation plays an important part in the desalination of saline water owing to its abundance in areas with potable water shortage and it also occupies a paramount place in green energy generation due to its simplicity of application. Still distiller is viewed by researchers as a suitable source of potable water because of low cost of fabrication, easy operation and zero emission technology. Studies by researchers are geared towards exploring new models to improve the productivity of solar stills and enhance its production rate is ongoing. The main aspiration of this work is to experiment the consequence of introducing a passive condenser to a modified conventional solar still to enhance its productivity yield. It was observed that the modified passive still distiller coupled with the external condenser gave about 11.85% higher production yield in comparison with the modified conventional still distiller. Daily and accumulated distillate yield for the still distillers have been studied and analyzed. The result of the findings revealed that sawdust padding around the still distillers is recommended to maximize productivity leading to efficient water distillation in regions where that require still distiller usage. This recommendation has been seen to produce the desired result in accessing to potable water within areas where water scarcity prevails. This is suggested to contribute effectively bearing the cost ineffective water desalination technique.

The air humidification-dehumidification (HDH) technique for water desalination can be useful in many water production applications. Researchers from all around the world have examined various implementations of this technology to improve it. The present research investigates the effect of three dehumidifier coolants on the system. These coolants include water, helium, and hydrogen. The impact of these coolants on the parameters of the humidification-dehumidification desalination system will be discussed. The investigation’s parameters are tested at various mass ratios, air flow rates, and air outlet heaters. The results show that when hydrogen is employed as a dehumidifier coolant, the gained output ratio (GOR) achieves its peak of 6.37 in the considered mass ratio range of 2.1 to 3. On the other hand, when hydrogen is utilized as a dehumidifier coolant, the system produces the maximum entropy, with the dehumidifier contributing the most. When the mass ratio changes from 2 to 3, the average entropy generation for the system using hydrogen in the dehumidifier increases by 3.8 and 2.9 times, respectively, compared to the average entropy generation for the system using water and helium. However, when hydrogen is used as a dehumidifier coolant, safety concerns must be addressed, as well as the size and cost of heat exchangers in comparison to water.

ABSTRACTPolyelectrolytes with strong acidic functionality are among the prime sources for water desalination techniques. Poly 2‐acrylamido‐2‐methylpropanesulfonic acid (PAMPS) is one such polymer showing polyelectrolyte characteristics because of highly acidic SO3H group (pKa < 2) and film‐forming characteristics of flexible polymeric chains. Halloysite nanotubes functionalized with polyelectrolytes can be considered for water purification, as halloysite was reported to be efficient in removing dissolved metal salts. These polyelectrolytes can be introduced as a blend with other components, or they can be synthesized via in situ to form flexible membranes. Polymer nano‐filtration membranes with controlled crosslinking were designed as a function of halloysite and AMPS composition using in situ free radical polymerization with other polymers such as polyvinylidene fluoride and polyvinylpyrrolidone to strengthen the polymer matrix. The synthesized membranes were characterized using FTIR, SEM, EDS, TGA, and DTG techniques. Equilibrium water content, contact angle, water flux, salt rejection efficiency, and antifouling studies are also carried out for these membranes in water purification.

Fabrication of PVDF membranes via VIPS-NIPS technique for water desalination: Effect of preparation condition

Abstract In this article, we explore the role of nanotechnology in addressing water scarcity through water desalination. The scope of nanotechnology in water treatment is discussed, emphasizing the potential of 2D nanomaterials such as hexagonal boron nitride (h-BN), graphene, and quantum dots in revolutionizing desalination technologies. Various water desalination techniques, including membrane distillation (MD), solar-powered multi-stage flash distillation (MSF), and multi-effect distillation (MED), are analyzed in the context of nanomaterial applications. The review highlights the energy-intensive nature of conventional water treatment methods and underscores nanomaterials’ potential to enhance efficiency and sustainability in water desalination processes. Challenges facing desalination, such as scalability and environmental impact, are acknowledged, setting the stage for future research directions.

Impact of chloride salts on TBAB/Methane and TBAB/Carbon dioxide semiclathrate hydrates: Application to desalination

Polyaniline/activated carbon composite based flowing electrodes for highly efficient water desalination with single-cycle operational mode

One-step fabrication of soot particle-embedded fibrous membranes for solar distillation using candle burning-assisted electrospinning

Boosted brackish water desalination and water softening by facilely designed MnO2/hierarchical porous carbon as capacitive deionization electrode

Desalination of produced water via CO2 + C3H8 hydrate formation

One of the emerging water desalination techniques relies on the compression of a polyelectrolyte gel. The pressures needed reach tens of bars, which are too high for many applications, damage the gel and prevent its reuse. Here, we study the process by means of coarse-grained simulations of hydrophobic weak polyelectrolyte gels and show that the necessary pressures can be lowered to only a few bars. We show that the dependence of applied pressure on the gel density contains a plateau indicating a phase separation. The phase separation was also confirmed by an analytical mean-field theory. The results of our study show that changes in the or salinity can induce the phase transition in the gel. We also found that ionization of the gel enhances its ion capacity, whereas increasing the gel hydrophobicity lowers the pressure required for gel compression. Therefore, combining both strategies enables the optimization of polyelectrolyte gel compression for water desalination purposes.

Poly-p-phenylene as a novel pseudocapacitive anode or cathode material for hybrid capacitive deionization

Flow-electrode capacitive deionization (FCDI) offers an electrochemical, energy-efficient technique for water desalination. In this work, we report the study of carbon-based FCDI, which consists of one desalination chamber and one salination chamber and applies a carbon nanomaterials-based flow electrode that circulates between the cell anode and cathode, to achieve a fast, continuous desalination process. Five different carbon nanomaterials were used for preparing the flow electrode and were studied for the desalination performance, with properties including average salt removal rate (ASRR), salt removal efficiency (SRE), energy consumption (EC) and charge efficiency (CE) being quantitatively determined for comparation. Different FCDI parameters, including carbon concentration and flow rate of the flow electrode and cell voltage, were investigated to examine the influences on the desalination. Long-term operation of the carbon-based FCDI was evaluated using the optimal results found in the conditions of 1.5 M concentration, 1.5 V cell voltage, and 20 mL min−1 flow rate of electrode and water streams. The results showed an ASRR of 63.7 µg cm−2 min−1, EC of 162 kJ mol−1, and CE of 89.3%. The research findings validate a good efficiency of this new carbon-based FCDI technology in continuous water desalination and suggest its good potential for real, long-term application.

Machine learning modelling of a membrane capacitive deionization (MCDI) system for prediction of long-term system performance and optimization of process control parameters in remote brackish water desalination

Climate change and water overextraction are some of the reasons for a growing global water stress, with seawater desalination being the leading solution worldwide. The state-of-the-art technology for seawater desalination is reverse osmosis (RO), utilizing mechanical pressure to push seawater through membranes, leaving the dissolved species in the brine. However, boron, which is considered toxic in high concentrations, is poorly removed by RO. This is because under normal conditions boron is present as boric acid, a small neutrally-charged compound. The most common technique to overcome this problem includes multiple RO stages combined with chemical dosage of the effluent, ensuring boron is present as borate, a charged species, present in high pH conditions.Capacitive deionization (CDI) is an emerging membraneless technique for water treatment and desalination, based on electrosorption of salt ions into microporous electrodes. Large internally-generated pH gradients develop during CDI operation, and thus CDI can potentially remove boron without chemically adjusting the feed pH. Here, we present a novel theoretical framework predicting the adsorption of boron in micropores, while considering pH-dependent chemical surface groups in the micropores, ion transport in the macropores, and local electrolyte pH. Moreover, we account for association and dissociation reactions of boron-consisting compounds in the electrolyte[1].We analyzed the effects electrodes order have on pH dynamics, where panels a. and b. in the attached figure present spatiotemporal plots of the pH for the case where cathode is placed upstream (panel a., cat-an) and the anode placed upstream (panel b., an-cat). This analysis shows that higher pH in the anode are expected for the an-cat configuration, counter to common-wisdom in the field. Panel c. follows this trend, by presenting the removed boron as a function of scaled flow velocity for both configurations. The results show, both experimentally and theoretically, that an-cat configuration should be preferred. Similarly, we found that an optimum charging voltage exists, even without accounting for parasitic reactions. Moreover, we found that also the discharging voltage significantly affects boron removal. Overall, CDI is a promising technology for boron removal, but a deep theoretical understanding of the problem is crucial towards future optimization.

Anti-biofouling photothermal film for solar steam generation based on oxygen defects rich and haloperoxidase mimic active V6O13

Capacitive deionization is an emerging and rapidly developing electrochemical technique for water desalination across the globe with exponential growth in publications. There are various architectures and materials being explored to obtain utmost electrosorption performance. The symmetric architectures consist of the same material on both electrodes, while asymmetric architectures have electrodes loaded with different materials. Asymmetric architectures possess higher electrosorption performance as compared with that of symmetric architectures owing to the inclusion of either faradaic materials, redox-active electrolytes, or ion specific pre-intercalation material. With the materials perspective, faradaic materials have higher electrosorption performance than carbon-based materials owing to the occurrence of faradaic reactions for electrosorption. Moreover, the architecture and material may be tailored in order to obtain desired selectivity of the target component and heavy metal present in feed water. In this review, we describe recent developments in architectures and materials for capacitive deionization and summarize the characteristics and salt removal performances. Further, we discuss recently reported architectures and materials for the removal of heavy metals and radioactive materials. The factors that affect the electrosorption performance including the synthesis procedure for electrode materials, incorporation of additives, operational modes, and organic foulants are further illustrated. This review concludes with several perspectives to provide directions for further development in the subject of capacitive deionization. PRACTITIONER POINTS: Capacitive deionization (CDI) is a rapidly developing electrochemical water desalination technique with exponential growth in publications. Faradaic materials have higher salt removal capacity (SAC) because of reversible redox reactions or ion-intercalation processes. Combination of CDI with other techniques exhibits improved selectivity and removal of heavy metals. Operational parameters and materials properties affect SAC. In future, comprehensive experimentation is needed to have better understanding of the performance of CDI architectures and materials.

Particle size distribution influence on capacitive deionization: Insights for electrode preparation

Flow capacitive deionization is a water desalination technique that uses liquid carbon-based electrodes to recover fresh water from brackish or seawater. This is a potential second-generation water desalination process, however it is limited by parameters such as feed electrode conductivity, interfacial resistance, viscosity, and so on. In this study, titanium oxide nanofibers (TiO2NF) were manufactured using an electrospinning process and then blended with commercial activated carbon (AC) to create a well distributed flow electrode in this study. Field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and energy dispersive X-ray (EDX) were used to characterize the morphology, crystal structure, and chemical moieties of the as-synthesized composites. Notably, the flow electrode containing 1 wt.% TiO2NF (ACTiO2NF 1 wt.%) had the highest capacitance and the best salt removal rate (0.033 mg/min·cm2) of all the composites. The improvement in cell performance at this ratio indicates that the nanofibers are uniformly distributed over the electrode’s surface, preventing electrode passivation, and nanofiber agglomeration, which could impede ion flow to the electrode’s pores. This research suggests that the physical mixture could be used as a flow electrode in capacitive deionization.