Search Results (46)

To overcome the limitations of insufficient driving force in traditional microbial desalination batteries, this paper constructs a microbial anode-membrane capacitive deionization (B-MCDI) coupling system. For the first time, direct coupling between extracellular electron transfer in Shewanella oneidensis and double-layer adsorption at the MCDI cathode is achieved at the circuit and material levels, realizing self-driven, low-energy desalination. High-specific-surface-area carbon felt is used as the anode, and a stable electrogenic biomembrane (output voltage >400 mV) is formed after directional domestication with Shewanella oneidensis MR-1. Activated carbon is used as the cathode to construct the MCDI electrode. In the three-chamber reactor, the desalination chambers are separated by cation and anion exchange membranes. Under the drive of the bioelectric field, Na⁺ and Cl⁻ selectively permeate into the cathode and anode chambers, respectively, effectively suppressing the co-ion effect. Under optimal operating conditions (external resistance 1000 Ω, initial NaCl concentration 2.0 g/L), the system achieved a cumulative desalination rate of 85.1% after 12 h of operation, with a salt adsorption capacity of 162.1 mg/g, an average desalination rate of 13.51 mg/(g·h), and an energy consumption of only 0.58 kWh/m³. This demonstrates that bioelectric energy can effectively provide targeted power to drive capacitive adsorption and desalination. Under initial NaCl concentrations of 1.0 g/L and 3.0 g/L, the highest desalination rates reached 78% and 68%, respectively. The maximum instantaneous desalination rate occurred within 0.5–1.0 h (64 mg/h under 2.0 g/L conditions), exhibiting a three-stage kinetic characteristic of “fast-slow-equilibrium”. The energy consumption in this study was only 0.51 kWh/m³, further demonstrating the high energy efficiency of bioelectrically coupled MCDI in low-salinity treatment areas. Therefore, this B-MCDI can serve as a theoretically feasible proof-of-concept technology for desalination of brackish water that meets the requirements of self-driven, low-energy consumption, and has promising applications in decentralized water supply systems in areas with limited energy supply or no available electricity. Full article

Chloride-induced corrosion is a major threat to excavated bronze artifacts, yet conventional alkaline desalination requires repeated solution replacement and generates secondary chemical waste. Herein, a series of BiOCl-loaded carbon nanofiber composites (CNFs@BiOCl-X) were prepared by KOH activation followed by hydrothermal growth of BiOCl, aiming to develop regenerable electrodes for chloride removal in capacitive deionization systems. Alkali activation regulated the surface roughness, oxygen-containing functional groups, hydrophilicity, and BiOCl loading of CNFs, while the three-dimensional conductive network helped immobilize BiOCl nanostructures and buffer the volume variation associated with reversible Bi/BiOCl conversion. Electrochemical analyses confirmed the pseudocapacitive chloride-storage behavior of the composites, with ion removal governed by the coupled effects of BiOCl redox activity, charge transfer, and interfacial ion transport. In a fixed-electrode membrane capacitive deionization system, CNFs@BiOCl-2 exhibited the best overall performance, delivering a salt adsorption capacity of 100.44 mg g⁻¹ at 1.4 V and retaining 93.17% of its desalination capacity after 35 cycles at 1.2 V. For flow-electrode capacitive deionization, the higher BiOCl-loading CNFs@BiOCl-5 showed superior utilization of active sites and achieved 94.75% NaCl removal from a 1000 mg L⁻¹ solution within 3 h, with an average desalination rate of 15.48 μg cm⁻² min⁻¹ and an energy consumption of 0.88 kWh kg⁻¹-NaCl. These findings demonstrate that rationally matching BiOCl loading with electrode configuration enables efficient and sustainable chloride management, offering a promising electrochemical strategy for conservation electrolytes and related desalination applications. Full article

Capacitive de-ionization (CDI) holds great promise for water desalination, while the widely used activated carbon (AC) electrodes suffer from a low salt adsorption capacity (SAC) and poor long-term stability due to the co-ion effect and electrode oxidation. Inspired by membrane-based CDI, we deposited polyethyleneimine (PEI), an ion exchange polymer with positive charge and ion selectivity, onto an AC electrode to serve as an anode for addressing these issues. Firstly, compared to traditional AC and commercial AEM-AC, the PEI-doped AC (PDAC) anode delivered a superior SAC of 36.3 mg/g, as the positively charged PEI enhanced electrostatic attraction, suppressed the co-ion effect, and offered extra sites. However, it showed poor cycling stability with 77.1% retention, owing to mass loss and anode oxidation. We further developed an electrode coated with a PEI-based membrane (PMAC), which exhibited a balanced performance with a high SAC of 33.4 mg/g and significantly improved long-term retention of 97.5%. The hydrophilic PEI membrane, strongly adhered to the AC surface, shortened the ion diffusion resistance and effectively prolonged the electrode lifespan. A systematic comparison between AC, AEM-AC, PDAC, and PMAC revealed the mechanism for PMAC’s notable enhancement. These findings establish a framework for designing novel CDI electrodes and advancing sustainable water desalination. Full article

This study compares the operational performance of membrane capacitive deionization (MCDI) and circulation-MCDI (C-MCDI) under symmetric (2/2, 3/3, 4/4 min) and asymmetric (5/2, 5/3, 5/4 min) adsorption/desorption cycles to identify efficient operating conditions at the pilot scale. A pilot system was tested with a NaCl solution of about 1000 mg/L, and 15 consecutive cycles were conducted to evaluate removal efficiency, specific energy consumption (SEC), and stability. MCDI consistently achieved over 90% removal efficiency with SEC below 0.6 kWh/m³ across all modes, maintaining stable performance over 15 cycles. The 2/2 condition provided the shortest cycle time and the highest treated water productivity, making it the most efficient condition for the pilot-scale MCDI tested. C-MCDI showed stronger dependence on operating conditions, with the number of stable cycles ranging from 3 to 7 depending on desorption duration. Nevertheless, the 5/2 condition achieved about 91% removal efficiency with 0.58 kWh/m³ SEC, and its extended adsorption period yielded about 2.5 times more treated water per cycle than the 2/2 case. Overall, this work provides a comparative pilot-scale evaluation of MCDI and C-MCDI, highlighting their advantages, limitations, and potential applications, and offering practical insights for energy-efficient and sustainable desalination strategies. Full article

Polypyrrole, which belongs to the conducting polymer family, has demonstrated profound potential in advanced water purification applications due to its inherent electrical conductivity, environmental stability, and tunable surface chemistry. As a sorbent, PPy exhibits high sorption capacity for aquatic contaminants, including heavy metals, pharmaceutical compounds, and their metabolites, as well as synthetic dyes. The removal efficiency is correlated to a complex interaction mechanism involving electrostatic attractions, redox activity, and π–π stacking. Recent advances have expanded the utility by further developing nanostructured PPy-based (nano)composites, which elevate sorption performance by increasing surface area, mechanical integrity, and selective affinity. In addition, its integration into membrane technologies has enabled the design of an effective filtration system with improved selectivity and regeneration capabilities. Moreover, PPy is effective in electrochemical processes of water treatment, including capacitive deionization and electrochemically assisted sorption, opening novel paths towards energy-efficient pollutant removal. The multifunctionality of PPy as a sorbent material highlights its value as an important material for water treatment, with the capability of extended modification tailored for emerging environmental needs revised in this work. Full article

Amid concurrent pressures on water and material resources, recovering valuable ions like lithium and nutrients from brines and wastewater is a critical tenet of the circular economy. This review provides a critical assessment of electro-driven membranes (EDMs) as a key technology platform for achieving this goal with high energy efficiency. A comprehensive synthesis and analysis of the current state-of-the-art of core EDM technologies, including electrodialysis (ED) and membrane capacitive deionization (MCDI), is presented, focusing the analysis on the performance metrics of specific energy consumption and ion selectivity. The findings reveal that the optimal EDM technology is highly application-dependent, with MCDI excelling for dilute streams and ED for concentrated ones. While significant advances in monovalent selective membranes have enabled lithium recovery, achieving high selectivity between ions of the same valence (e.g., Li⁺/Na⁺) remains a fundamental challenge. Moreover, persistent issues of membrane fouling and scaling continue to inflate energy consumption and represent a major bottleneck for industrial-scale deployment. While EDMs are a vital technology for ion resource recovery, unlocking their full potential requires a dual-pronged approach: advancing materials science to design novel, highly selective membranes, while simultaneously developing intelligently integrated systems to surmount existing performance and economic barriers. Full article

This study presents a sustainable approach for synthesizing high-performance activated carbon from Spirulina Alga through hydrothermal carbonization followed by chemical activation using potassium hydroxide. The resulting activated carbon exhibited a high Brunauer–Emmett–Teller (BET) surface area of 1747 m²/g and a total pore volume of 1.147 cm³/g, with micropore volume accounting for 0.4 cm³/g. Characterization using Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy (SEM-EDS), X-ray Photoelectron Spectroscopy (XPS), and gas adsorption analyses confirmed the presence of hierarchical micro- and mesoporosity as well as favorable surface functional groups. The synthesized carbon was used to fabricate electrodes for membrane capacitive deionization (MCDI) along with cation and anion-selective membranes, which were then tested with saline water (500–5000 ppm) and synthetic hard water (898 ppm of total salts). The salt adsorption capacity (SAC) reached 25 (batch) to 40 (continuous) mg/g, while rapid adsorption rates with average salt adsorption rates (ASARs) values exceeding 10 (batch) to 30 (continuous) mg·g⁻¹·min⁻¹ during early stages were obtained. Batch MCDI experiments demonstrated a higher SAC compared to continuous operation, with non-monotonic trends in SAC observed as a function of feed concentration. Ion adsorption kinetics were influenced by ion valency, membrane selectivity, and pore structure. The specific energy consumption (SEC) was calculated as 8–21 kJ/mol for batch and 0.1–0.5 kJ/mol for continuous process. These performance metrics are on par with or surpass those reported in the recent literature for similar single-electrode CDI configurations. The results demonstrate the viability of using Alga-derived carbon as an efficient and eco-friendly electrode material for water desalination technologies. Full article

Microfluidic techniques have emerged as promising, efficient, cost-effective, and environmentally friendly desalination solutions. By utilizing fluid dynamics at the microscale, these techniques offer precise control over chemical, biological, and physical processes, presenting advantages such as reduced energy consumption, miniaturization, portability, and enhanced process control. A significant challenge in scaling microfluidic desalination for macro applications is the disparity in flow rates. Current devices operate at microliters per minute, while practical applications require liters daily. Solutions involve integrating multiple units on a single chip and developing stackable chip designs. Innovative designs, such as 3D microfluidic chips, have shown promise in enhancing scalability. Fouling, particularly in seawater environments, presents another major challenge. Addressing fouling through advanced materials, including graphene and nanomaterials, is critical to improving the efficiency and longevity of devices. Advances in microfluidic device fabrication, such as photo-patterned hydrogel membranes and 3D printing, have increased device complexity and affordability. Hybrid fabrication approaches could further enhance membrane quality and efficiency. Energy consumption remains a concern, necessitating research into more energy-efficient designs and integration with renewable energy sources. This paper explores various electrochemical-based microfluidic desalination methods, including dialysis/electrodialysis, capacitive deionization (CDI)/electrochemical capacitive deionization (ECDI), ion concentration polarization (ICP), and electrochemical desalination (ECD). Full article

Salinity gradient power (SGP) technologies, including pressure-retarded osmosis (PRO) and reverse electrodialysis (RED), have the potential to be utilized for the purpose of harvesting energy from the difference in salinity between two water streams. One challenge associated with SGP is a reduction in power density due to membrane fouling when impaired water is utilized as a low-salinity water stream. Accordingly, this study sought to explore the feasibility of membrane capacitive deionization (MCDI), a low-energy water treatment technique, as a novel pretreatment method for SGP. Laboratory-scale experiments were conducted to evaluate the impact of MCDI pretreatment on the performance of PRO and RED. The low-salinity water was obtained from a brackish water reverse osmosis (BWRO) plant, while the high-salinity water was a synthetic seawater desalination brine. The removal efficiency of organic and inorganic substances in brackish water reverse osmosis (BWRO) brine by MCDI was estimated, as well as theoretical energy consumption. The results demonstrated that MCDI attained removal efficiencies of up to 88.8% for organic substances and 78.8% for inorganic substances. This resulted in a notable enhancement in the lower density for both PRO and RED. The power density of PRO exhibited a notable enhancement, reaching 3.57 W/m² in comparison to 1.14 W/m² recorded for the BWRO brine. Conversely, the power density of RED increased from 1.47 W/m² to 2.05 W/m². Given that the energy consumption by MCDI is relatively low, it can be surmised that the MCDI pretreatment enhances the overall efficiency of both PRO and RED. However, to fully capitalize on the benefits of MCDI pretreatment, it is recommended that further process optimization be conducted. Full article

The rapid expansion of lithium-ion battery (LIB) markets for electric vehicles and renewable energy storage has exponentially increased lithium demand, driving research into sustainable extraction methods. Traditional lithium recovery from brine using evaporation ponds is resource intensive, consuming vast amounts of water and causing severe environmental issues. In response, Direct Lithium Extraction (DLE) technologies have emerged as more efficient, eco-friendly alternatives. This review explores two promising electrochemical DLE methods: Electrodialysis (ED) and Capacitive Deionization (CDI). ED employs ion-exchange membranes (IEMs), such as cation exchange membranes, to selectively transport lithium ions from sources like brine and seawater and achieves high recovery rates. IEMs utilize chemical and structural properties to enhance the selectivity of Li⁺ over competing ions like Mg²⁺ and Na⁺. However, ED faces challenges such as high energy consumption, membrane fouling, and reduced efficiency in ion-rich solutions. CDI uses electrostatic forces to adsorb lithium ions onto electrodes, offering low energy consumption and adaptability to varying lithium concentrations. Advanced variants, such as Membrane Capacitive Deionization (MCDI) and Flow Capacitive Deionization (FCDI), enhance ion selectivity and enable continuous operation. MCDI incorporates IEMs to reduce co-ion interference effects, while FCDI utilizes liquid electrodes to enhance scalability and operational flexibility. Advancements in electrode materials remain crucial to enhance selectivity and efficiency. Validating these methods at the pilot scale is crucial for assessing performance, scalability, and economic feasibility under real-world conditions. Future research should focus on reducing operational costs, developing more durable and selective electrodes, and creating integrated systems to enhance overall efficiency. By addressing these challenges, DLE technologies can provide sustainable solutions for lithium resource management, minimize environmental impact, and support a low-carbon future. Full article

Membrane capacitive deionization (MCDI) is an electrochemical ion separation process that combines ion-exchange membranes (IEMs) with porous carbon electrodes to enhance desalination efficiency and address the limitations of conventional capacitive deionization (CDI). In this study, a cation-exchange membrane (CEM) embedded with a metal–organic framework (MOF) was developed to effectively separate monovalent and multivalent cations in influent solutions via MCDI. To fabricate CEMs with high monovalent ion selectivity, ZIF-8 was incorporated into sulfonated poly(2,6-dimethyl-1,4-phenylene oxide) (SPPO) at various weight ratios. The resulting membranes were systematically characterized using diverse electrochemical methods. The ZIF-8-embedded CEMs demonstrated a sieving effect based on differences in ion size and hydration energy, achieving excellent permselectivity for monovalent ions. MCDI tests using the prepared CEMs showed a Na⁺ ion removal rate exceeding 99% in Na⁺/Mg²⁺ and Na⁺/Ca²⁺ mixed feed solutions, outperforming a commercial membrane (CSE, Astom Corp., Tokyo, Japan), which achieved a removal rate of 94.1%. These findings are expected to provide valuable insights for advancing not only MCDI but also other electro-membrane processes capable of selectively separating specific ions. Full article

Ensuring the sustainability of a product or a system requires a thorough evaluation of its environmental and socioeconomic impacts. In this context, one of the objectives of the EU-PRIMA SmaCuMed project is to evaluate the socioeconomic and environmental impacts of the Smart Cube system. The Smart Cube was developed for the PV-powered desalination of brackish groundwater with membrane capacitive deionization (MCDI) and low-pressure reverse osmosis (LPRO); it additionally uses smart sensors for controlled irrigation in remote agricultural areas in Morocco, as an example for the North African region. Based on the Life Cycle Sustainability Assessment approach, this paper aims to assess the environmental and economic impacts of the Smart Cube, using Life Cycle Costing (LCC) and Life Cycle Assessment (LCA) analyses for environmental evaluation. Various scenarios have been defined for both environmental and economic assessments. Based on 1 m³ of produced desalinated water, the LCC results showed that, when using the desalination technologies directly connected to the grid, the prices are lower than those obtained when it was supplied by the PV system. This is only due to the very low energy prices from the Moroccan grid (EUR 0.10/kWh). The LCC results showed that LPRO is a more cost-effective option for producing desalinated water, with a lower total cost compared to MCDI. However, LCA results indicated that LPRO has a higher environmental impact compared to MCDI. If higher water production capacity is a priority, MCDI connected to PV is the best choice, with lower carbon emission but higher overall water costs. Full article

In this study, we developed a pilot-scale membrane capacitive deionization (MCDI) system for treating mildly brackish water and examined various operational parameters, including module arrangements, adsorption/desorption times, and flow rates. As we aimed to optimize these parameters to increase total dissolved solids (TDS) removal efficiency, the results revealed that the dual-series mode module arrangement and an adsorption time of 120 s with a flow rate of 10 L/min achieved the highest TDS removal efficiency of 99%. Energy consumption analysis showed that lower flow rates were associated with higher TDS removal efficiencies, highlighting the balance between energy consumption and water quality. This study provides insights into optimizing a pilot-scale MCDI for efficient water supply solutions, offering promise for sustainable and eco-friendly water treatment. Full article

The use of saline water resources in agriculture is becoming a common practice in semi-arid and arid regions such as the Mediterranean. In the SmaCuMed project, the desalination of brackish groundwater (TDS = 2.8 g/L) for the irrigation of Argan trees in Essaouira, Morocco, to 2 g/L and 1 g/L (33% and 66% salt removal, respectively) using low-pressure reverse osmosis (LPRO) (p < 6 bar) and membrane capacitive deionization (MCDI) was tested at pilot scale. MCDI showed 40–70% lower specific energy consumption (SEC) and 10–20% higher water recovery; however, the throughput of LPRO (2.9 m³/h) was up to 1.5 times higher than that of MCDI. In addition, both technologies were successfully powered by PV solar energy with total water costs ranging from EUR 0.82 to EUR 1.34 per m³. In addition, the water quality in terms of sodium adsorption ratio was slightly higher with LPRO resulting in higher concentrations of Ca²⁺ and Mg²⁺, due to blending with feed water. In order to evaluate both technologies, additional criteria such as investment and specific water costs, operability and brine disposal have to be considered. Full article

Another technique for desalination, known as membrane capacitive deionization (MCDI), has been investigated as an alternative. This approach has the potential to lower the voltage that is required, in addition to improving the ability to renew the electrodes. In this study, the desalination effectiveness of capacitive deionization (CDI) was compared to that of MCDI, employing newly produced cellulose acetate ion exchange membranes (IEMs), which were utilized for the very first time in MCDI. As expected, the salt adsorption and charge efficiency of MCDI were shown to be higher than those of CDI. Despite this, the unique electrosorption behavior of the former reveals that ion transport via the IEMs is a crucial rate-controlling step in the desalination process. We monitored the concentration of salt in the CDI and MCDI effluent streams, but we also evaluated the pH of the effluent stream in each of these systems and investigated the factors that may have caused these shifts. The significant change in pH that takes place during one adsorption and desorption cycle in CDI (pH range: 2.3–11.6) may cause problems in feed water that already contains components that are prone to scaling. In the case of MCDI, the fall in pH was only slightly more noticeable. Based on these findings, it appears that CDI and MCDI are promising new desalination techniques that has the potential to be more ecologically friendly and efficient than conventional methods of desalination. MCDI has some advantages over CDI in its higher salt removal efficiency, faster regeneration, and longer lifetime, but it is also more expensive and complex. The best choice for a particular application will depend on the specific requirements. Full article