Ion Exchange Research Articles

Effective Removal of Sr2+ Ions by K2SbPO6/Polyacrylonitrile Composite Microspheres

90Sr is one of the highly radioactive and hazardous nuclides in nuclear waste liquids. The high water solubility and mobility of 90Sr2+ ions make it difficult to effectively remove 90Sr from the complex aqueous environment. Herein, K2SbPO6, a phosphatoantimonate ion exchange material with an excellent removal ability for Sr2+ ions, has been organically granulated with polyacrylonitrile (PAN) by an automated method to form K2SbPO6/PAN composite microspheres. The K2SbPO6/PAN microspheres with radiation resistance exhibit a high maximum adsorption capacity (qmSr) of 131.15 mg g−1 for Sr2+ ions and retain the high removal rate (RSr) in a wide pH range (pH = 3–12). It is important that K2SbPO6/PAN microspheres could efficiently treat Sr2+ ions solutions in a dynamic adsorption manner even at 970 bed volumes (RSr > 81%). This work paves the way for the preparation of low-cost ion exchange materials with the advantages of regular shape and easy operation by a simple and fast method and the practical application of powdered ion exchange materials.

Fast Seawater Desalination Integrated with Electrochemical CO2 Reduction.

Coupling desalination with electrocatalytic reactions is an emerging approach to simultaneously addressing freshwater scarcity and greenhouse gas emissions. However, the salt removal rate in such processes is slow, and the applicable water sources are often limited to those with high salt concentrations. Herein, we show high-performance electrocatalytic desalination by coupling with electrochemical CO2 reduction using a carbon catalyst. A ZIF-8-derived carbon catalyst embedded with Cu nanoparticles delivers a high Faradaic efficiency of 94.3% for CO production at 288 μmol cm-2 h-1. The efficient CO2 electroreduction generates high current densities, which drive fast salt ion transfer across ion exchange membranes. The integrated device enables one of the quickest salt removal rates of 1043.49 μg cm-2 min-1 among various desalination methods. Drinking water can be obtained with an ion removal rate of 99% when natural seawater is used as the water source.

Dynamic kinetic studies of lysozyme removal as protein waste using weak ion exchange nanofiber membranes in flow systems: Linear and nonlinear model analysis

BackgroundThis study explores lysozyme removal using a weak ion exchange nanofiber membrane in a continuous flow system. Understanding removal kinetics is critical for designing, optimizing, and scaling industrial processes. Kinetic models play a crucial role in predicting removal behaviors, including the pseudo-first-order, pseudo-second-order, Elovich, Avrami, and intra-particle diffusion models. Each model provides different insights based on its assumptions, making them suitable for analyzing various removal systems and mechanisms. MethodsThe study investigated the effects of four parameters—removal pH, initial lysozyme concentration, loading flow rate, and the number of membranes stacking layers—on dynamic kinetic binding behavior. Both linear and non-linear kinetic models were employed to analyze experimental results, focusing on removal rates and mechanisms. Significant FindingsAnalysis revealed key insights into removal kinetics. The change in removal pH significantly affected the binding rate and capacity. Higher initial concentrations increased binding rates, while changes in loading flow rate influenced removal rate and capacity. Increasing the number of membrane stacking layers enhanced the removal capacity and increased the pressure drop. These findings underscore the importance of optimizing parameters for efficient removal in biotechnology and wastewater treatment.

Hybrid organic - inorganic filter system for cadmium ions adsorption from aqueous solutions

The study reflects on the problem of heavy metals, namely cadmium, polluting the natural environment. The goal was to select the most efficient adsorber enabling ion exchange between calcium and cadmium in an aqueous environment and subsequently design a material hybrid organic-inorganic, particle-fiber system that adsorbs cadmium from aqueous environments and will be easily included in the technological process. The novelty of this study lies in the use of waste food material – eggshells as a source of biogenic nanoparticles. These are applied to a nanofibrous structure made of polyvinyl butyral in amounts of 8 to 10 %wt by weight by the AC electrospinning. (The experiment was performed with these boundary conditions: temperature was 23°C, and humidity was 42%. The high-electrical voltage amplifier generated a sinusoidal waveform with a frequency of 50 Hz and an amplitude of 32 kV) and were used for ion exchange. In ion exchange, cadmium ions are exchanged with calcium ions based on the principle of chemical similarity of the two elements expressed by the z/r ratio (charge/ radius ratio), the z/r ratio is 2.02 for calcium ions Ca2+ and 2.06 for cadmium Cd2. Separateted nanoparticles of calcium carbonate obtained by burning eggshells (727°C) with dimensions from 100 to 200 nm and a specific surface area of 3.9 m2/g showed the highest adsorption capacity of 99.8%, synthetic calcium carbonate at 71.8%, and ground eggshells the lowest at 25.0%. Designed and laboratory-tested filter system of nanoparticles - nanofibers captures 95.6% and 96.8% of cadmium ions from an aqueous solution within 10 minutes and 90 minutes, respectively, at a concentration of cadmium ions of 10 mg/l, and at several nanoparticles of 0.3 g. The ion exchange is carried out only on the filter surface, and after a specific time, the calcium carbonate nanoparticles are released from the filter probably due to absence of chemical bond between nanoparticles and nanostructures or the low density of the nanofibrous structure. SEM, EDX, FTIR, BET and TGA analysis were used for material evaluation. The adsorption capacity of used nanoparticles and filter adsorbers was evaluated according to residual amounts of cadmium ions in aqueous solutions using ICP-IOS.

Cyclic Removal and Destruction of Per- and Polyfluoroalkyl Substances from Water Using Ion Exchange, Resin Regeneration, and UV/Sulfite Reduction

Ion exchange (IX) can effectively remove per- and poly-fluoroalkyl substances (PFAS) from drinking water sources at ng/L to µg/L levels. However, adsorbed PFAS on spent resins should be further destructed for detoxification. Traditional resin incineration or landfilling may cause secondary pollution to the surrounding environment and cannot achieve resin reuse. This study explored three variations of a PFAS treatment train, aiming to completely defluorinate PFAS with different chain lengths and functional groups at environmentally relevant levels (ng/L) and to reuse the resins and solvents. The optimized treatment train includes IX, resin regeneration with 5wt% NaCl and 60% v/v methanol, distillation of waste regenerant, and advanced reduction by hydrated electrons (eaq−) generated during the ultraviolet/sulfite (UV/sulfite) treatment of still bottoms. Such a treatment train achieved nearly 100% PFAS removal from surface water and groundwater using either PFAS-specific or generic resins, and almost 100% defluorination of PFAS except a few short-chain fluorinated sulfonates and ethers. Regenerated resins had comparable PFAS removal to the pristine resins over three cycles. The generic resins (e.g., Dupont AmberLite™ IRA910) are easier to regenerate and thus are recommended for the treatment train over PFAS-selective resins (e.g., Purofine® PFA694E). Direct heterogenous defluorination on resins loaded with perfluorooctane sulfonate (PFOS) was ineffective, potentially due to the consumption of UV light/eaq− by the resins and insufficient contact between the UV light/eaq− with PFOS on the resin surface. Distillation of the waste regenerant successfully concentrated PFAS in the still bottoms, reduced the waste volume, and removed excess methanol, all essential for effective UV/sulfite treatment. Meanwhile, the produced condensate with high methanol contents and low PFAS levels can be reused for the next regeneration cycle. Findings from this study provide a timely and sustainable solution to the stringent and evolving regulations on PFAS and the resultant production of PFAS-laden resins as hazardous wastes.

High efficiency removal of Cs+ by Fe-Co framework PBAs from radioactive wastewater

The widespread application of nuclear energy has increased the risk of contamination by radionuclide 137Cs. Prussian blue analogues are considered to be excellent materials for the removal of 137Cs from wastewater due to their unique structure. In this work, Cs+ adsorbent for PBAs with Fe-Co framework, potassium iron hexacyanocobaltate (PBAFe), was synthesized by room temperature precipitation method. Systematic structural characterization and performance results of PBAFe showed that it has a specific surface area of 452.8 m2/g and an average pore size of 8.6nm, providing more active sites for Cs+. The adsorption of Cs+ on PBAFe exhibited fast reaction kinetics (within 10min) and high adsorption capacity (82.90mg/g), and the removal rate of Cs+ reached 98.57%. The efficient removal of Cs+ by PBAFe in various real water environments showed its excellent selectivity and potential for practical application. In addition, adsorption mechanism studies showed that the adsorption of Cs+ was achieved by ion exchange with K+ in the PBAFe lattice. PBAFe has the advantages of simple synthesis and good selectivity, and has potential application in the harmless treatment of Cs+ in radioactive wastewater.

Sustainable stabilization/solidification of electroplating sludge using a low-carbon ternary cementitious binder

Electroplating sludge (ES), due to its high dosages of heavy metals (HMs), is classified as hazardous waste, presenting risks to both health and environment. Stabilization/solidification (S/S) technology is extensively applied in ES treatment. This study designs a low-carbon ternary cementitious binder, limestone calcined clay cement (LC3), for S/S treatment of ES and investigates the immobilization mechanism of HMs in the crystalline products and calcium alumino-silicate hydrate (C-A-S-H) within LC3. Results show that CrO42- and Cd2+ are primarily stabilized in aluminate crystalline products by replacing SO42- and Ca2+ in the double-layered plate structure, respectively. The remaining CrO42- is captured by the (SiOOH)2AlCa⁺ groups in C-A-S-H generated from substitution of aluminum tetrahedra to bridging silicon tetrahedra. For positively charged Cd2+, it is mainly stabilized through ion exchange with Ca2+ on the C-A-S-H chains. The pozzolanic reaction of calcined clay increases the Al/Ca and Si/Ca atomic ratios in C-A-S-H, enhancing the immobilization efficiency of C-A-S-H to CrO42- and Cd2+. The synergistic effect of calcined clay and limestone, along with the dissolution of aluminosilicates in calcined clay, changes the structure and composition of hydration products, facilitating the chemical binding of CrO42- and Cd2+ by aluminate products. Moreover, the extra hydration products generated by the pozzolanic reaction and the formation of numerous carboaluminate phases strengthen the physical encapsulation performance to HMs. Regarding actual S/S performance, multi-scale evaluation results show that the designed LC3 binder achieves sustainable S/S of ES with high strength, low carbon emission, low cost, and low energy consumption.

ZnFe-LDH synthesized by seed-induced method to simultaneous enhance arsenic removal, stabilization and sludge reduction

To simultaneously enhance arsenic removal, stabilization and sludge reduction, a seed-induced method was applied to in-stiu synthesize ZnFe-LDH containing arsenic (ZnFe-As-LDH). The optimal seed was determined to be ZnFe-LDH by analyzing the effects of the unseeded system and seed-induced system (FeⅡFeⅢ-LDH, ferrihydrite and ZnFe-LDH). In the ZnFe-LDH seed system, the arsenic removal efficiency increased and the arsenic leaching concentration were drastically reduced by 91.33% under the optimal conditions as the seeds dosage of 2.5g/L, pH 10 and Zn/Fe ratio of 1.5. The addition of seed crystals promoted crystal growth and aggregation and finally regulated the formation of dense bulk LDH with fewer pores and smaller pore sizes. The arsenic removal and stabilization were achieved by converting active arsenic into more stable crystalline bound arsenic through coprecipitation, ion exchange and complexation. The SV30 was reduced by 73.68% and it was due to reduction of unstable surface water and interspace and crystallinity enhancement. The formation pathway of ZnFe-As-LDH by seed-induced was elucidated. The seed-induced method promoted the formation of arsenic-containing ferrihydrite and Zn(OH)2 coprecipitations on the surface of ZnFe-LDH seed, and led to a structural rearrangement to generate ZnFe-As-LDH.

In situ preparation of carbon/zeolite composite materials derived from coal gasification fine slag for removing malachite green: Performance evaluation and mechanism insight

The stockpiling of coal gasification fine slag (CGFS) and the discharge of organic wastewater pose serious environmental threats. The complex synthesis process and limited pollutant removal capacity of CGFS-based adsorbents impede their efficient utilization in organic wastewater purification. In this work, carbon/zeolite composite materials (CZCM) derived from CGFS were prepared in situ using a one-pot method without further crystallization, achieving an ultra-high adsorption capacity (9705 mg/g) and excellent renewability for malachite green (MG). CZCM was identified as a typical mesoporous material with an abundant pore structure, facilitating the migration of MG within the material. Notably, various metal elements (e.g., iron and calcium) and chemical groups (e.g., carboxyl and hydroxyl) from CGFS were retained through this novel preparation method, providing additional adsorption sites and enhancing MG adsorption. The adsorption kinetics and thermodynamics results indicated that physisorption and multilayer adsorption were the primary adsorption modes of MG by CZCM, with the adsorption rate limited by internal diffusion. Furthermore, the adsorption process was found to be exothermic, spontaneous, and entropy-decreasing. Mechanistic investigations revealed that the exceptional adsorption performance of MG by CZCM was primarily attributed to electrostatic attraction and ion exchange, with hydrogen bonding and π-π interactions also playing significant roles. This study provides new insights into the development of CGFS-based adsorbents for organic wastewater treatment, promoting the efficient conversion and practical application of CGFS.

Adsorption characteristics and mechanism of novel ink melanin composite modified chitosan for Cd(II) in water

In this study, chitosan (CS), carboxymethyl chitosan (CMCS), and chitosan quaternary ammonium salt (HACC) were successfully loaded with ink melanin (ME) as efficient adsorbents for Cd(II) removal. The results of batch adsorption experiments and structural characterization showed that the modified CS loaded with ME improved the adsorption capacity of the composites for Cd(II). The pseudo-second-order kinetic and Langmuir equations were better suited to describe the batch adsorption experiments. The adsorption of Cd(II) was chemisorption with desirable adsorption effect when the concentration of the three composites was 0.5 mg/mL and the pH value was neutral. Among them, HACC-ME demonstrated remarkable Cd(II) adsorption performance (107.18 mg/g) and sustained an 85 % efficiency in Cd(II) removal over five adsorption-desorption cycles. Ion exchange, complexation, electrostatic attraction, and hydrophobic interaction were the primary mechanisms for Cd(II) removal. Overall, HACC-ME could be employed as a low-cost and highly efficient new natural adsorbent material for the removal of Cd(II) ions from wastewater. These findings illuminate pathways for the development of efficient and novel natural adsorbent materials for environmental cleanup purposes.

Novel MOF-derived hexagonal starfish-shaped hollow prismatic cone-loaded metal complexes for electrocatalytic water decomposition study

Exploring efficient and stable bifunctional electrocatalysts for oxygen evolution reaction/hydrogen evolution reaction (OER/HER) is an urgent need and challenge for sustainable energy. Non-noble metal-based catalysts have attracted more and more attention due to their low cost and high catalytic performance. The construction of heterostructures is considered to be one of the most promising strategies for revealing the efficient performance for OER and HER. As a result, we prepared a nanomaterial catalyst based on the combination of three non-precious metals, which were simultaneously used for efficient OER, HER and integral water splitting techniques. We first prepared a very novel hollow hexagram star-shaped metal-organic frameworks (MOFs) by a one-step hydrothermal method, then used it as the substrate material, introduced Mo6+ and Fe3+ through ion exchange reaction, and finally formed a composite system of Co3Fe7 and Mo2C through high-temperature calcination, and the product with hexagonal starfish morphology was named as hexagonal starfish-shaped hollow prismatic cone-loaded metal complexes (HSHP-Mo2C/Co3Fe7). Taking advantage of the synergistic effect of the Co3Fe7 site and the Mo2C site, HSHP-Mo2C/Co3Fe7 not only exhibit excellent OER and HER properties, but also exhibit good stability and durability. Specifically, the optimal catalyst HSHP-Mo2C/Co3Fe7-1 shows a Tafel slope of only 46mV dec-1 for OER and 99mV dec-1 fort HER, an overpotential of only 324 and 371mV and the stability is even up to 60h. This work provides a promising strategy for the development of cost-effective, efficient and stable catalysts for energy area.

Predicting ion exchange resin performance for contaminant removal from comingled groundwater plumes

Predicting ion exchange resin performance for contaminant removal from comingled groundwater plumes

Multidimensional octahedron (de) intercalation cathode for aqueous zinc-ion battery

CuS is a suitable material for use in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Nevertheless, the Zn2+ reaction between CuS is challenging due to the high radius and the considerable electrostatic force between the Zn2+ and CuS cathode. In this work, CuS nanosheets were in situ grown on a template surface via the hydrothermal method. The composition, surface morphology, and microstructure were then studied in detail. The zinc storage properties and mechanism were investigated through electrochemical testing, density functional theory and molecular dynamics simulation. The findings demonstrate that CuS nanosheets are formed in situ along the octahedral surface, resulting in the development of multistage structures. The distinctive configuration is capable of efficaciously preventing nanosheet aggregation, augmenting the specific surface area and active site of electrochemical reactions. Furthermore, the formation of a hollow structure through ion exchange reduces the intercalation energy barrier of Zn2+, facilitates rapid ion diffusion, enhances the charge transfer rate, and markedly improves battery performance.

Construction of low-vacancy hexagonal Prussian blue analogues for efficient rubidium recovery

Prussian blue analogues (PBAs) are considered a promising adsorbent for rubidium recovery due to their high ion exchange capacity and selectivity. However, the development of PBAs-based rubidium adsorbents with excellent stability and adsorption capacity is still hindered by the inevitable CN ligand vacancies. Herein, a synthetic strategy is proposed to slow down crystal nucleation and promote the self-repair of crystal defects by incorporating N-doped porous carbon (NPC) as a solid modifier during the synthesis process. As a result, the vacancy content of Zn-PBA-NPC is significantly decreased and large size twinned crystals are produced, which remarkably improves the thermal and acid-base stability. Benefiting from the high content of K+ in the low-vacancy Zn-PBA-NPC, it achieves a high adsorption amount of 199.1 mg/g and rapid adsorption kinetics of just 5 min for Rb+. In addition, it shows good selectivity in the presence of other alkali metal ions. This work not only prepares a high-performance adsorbent for efficient recovery of Rb+, but also facilitates insights into the design and construction of low-vacancy PBAs.

Scaling down recombinant carbonic anhydrase isolation with immobilized metal ion chromatography (IMAC): Harnessing enzymatic carbon dioxide capture and mineralization

BackgroundHuman activities have led to increased atmospheric CO2 levels, raising concerns about climate change. Carbonic anhydrase (CA) enzymes show promise for transforming CO2 into valuable products like calcium carbonate (CaCO3) through mineralization. Purifying and immobilizing CA enzymes on nanofiber membranes enhances their catalytic activity, enabling efficient CO2 conversion and mineralization. MethodsRecombinant CA was purified using immobilized metal affinity chromatography (IMAC), optimizing pH, biomass concentration, flow rate, and loading volume for maximum efficiency. The CA enzyme was then immobilized onto a weak ion exchange nanofiber membrane functionalized with AEA-COOH to create the CA-modified membrane (AEA-COOH-CA), enhancing CO2 conversion and CaCO3 mineralization. Significant findingsOptimal purification conditions (pH 7, 1 % biomass, 0.1 mL/min flow rate, 1.0 mL loading volume) were determined using IMAC. The CA-modified membrane effectively converted CO2 and mineralized CaCO3, demonstrating the potential for environmental CO2 sequestration. The immobilized CA activities of the AEA-COOH-CA nanofiber membranes exhibited 473.42 WAU/g-membrane, corresponding to 7.10 WAU per membrane piece. The CaCO3 precipitation reached 83.90 mg, with a precipitation efficiency of 11.82 mg CaCO3/WAU. These findings underscore the promise of enzymatic carbon capture using CA-modified membranes, offering a sustainable solution for greenhouse gas mitigation.

Ion exchange for enhancing MOF adsorbents performance in humid C2H2/CO2 separation

Ion exchange for enhancing MOF adsorbents performance in humid C2H2/CO2 separation

Red-emitting phosphors NaLiXF6:Mn4+ (X = Ti, Si) for white LEDs with high color rendering index and low correlated color temperature

White light-emitting diodes (WLEDs) are widely used in various lighting applications due to their high brightness and energy efficiency. However, commercial WLEDs, which typically combine YAG:Ce3+ phosphors with blue light-emitting diode chips, often lack red components, resulting in a high correlated color temperature (CCT) and a low color rendering index (CRI). To address this issue, two novel Mn4+-doped red-emitting phosphors, NaLiTiF6 and NaLiSiF6, were synthesized using an ion exchange method. Both phosphors exhibit strong red light with a pronounced zero-phonon line (ZPL) emission under blue light excitation. Optimal photoluminescence emission intensities were observed at Mn4+ concentrations of 6% for NaLiTiF6 and 9% for NaLiSiF6. When the temperature increased from 303 K to 413 K, both phosphors demonstrated outstanding brightness and chromatic stability. Integrated into phosphor-converted light-emitting diodes (pc-LEDs), the device incorporating NaLiTiF6:6%Mn4+ achieved a CRI of 95.1 and a CCT of 3172 K, while the device with NaLiSiF6:9%Mn4+ showed a CRI of 87.9 and a CCT of 3784 K. In addition, the luminous efficacy, CRI, and CCT of both prototype pc-LEDs maintained minimal variation with increasing driving current. These results indicate the stability and suitability of the synthesized phosphors for enhancing the performance of warm WLEDs applications.

Comparison of cost and performance between traditional and green processes for producing bimetallic carbide based oxygen reduction electrocatalysts

Chemical (ion exchange resin) and biomass (water hyacinth leaves) as carbon precursors are adopted to prepare two kinds of bimetallic carbide (Fe2MoC)-based catalytic materials. It is found that, compared with the material that use ion-exchange resin as carbon precursor (N-Fe2MoC-RG), the material that use water hyacinth as carbon precursor (N-Fe2MoC-WHG) has more advantages in cost, environment protection, synthesis simplicity, and catalytic activity for oxygen reduction reaction (ORR). Therein, the N-Fe2MoC-WHG as a cathode catalyst displays a half-wave potential of 0.905 V (vs. RHE) for catalyzing ORR in alkaline media, and gets a high peak power density of 1.52 W cm-2 in alkaline electrolyte membrane fuel cell; moreover, the N-Fe2MoC-WHG displays higher power-density retention or growth rate at lower relative humidity, higher back pressure, higher working temperature and higher catalyst loading, compared with the N-Fe2MoC-RG. The N-Fe2MoC-WHG is one of the most active precious metal-free catalysts reported so far, and its stability is very excellent.

Ultrasonic chemical synthesis of zinc-manganese ferrites with improved magnetic properties

Zinc-Manganese spinel ferrites (Zn1-xMnxFe2O4) are nowadays very attractive magnetic materials for cancer diagnostic and therapy. With the help of intense ultrasonic waves, sonochemical synthesis method was used to prepare stoichiometric and chemically homogenous nanoparticles by varying the manganese content. The crystal structure along with the size and shape of the as-prepared nanoparticles were described using XRD, TEM and FT-IR techniques, while cations distribution was carefully investigated using XPS and Mössbauer spectroscopic techniques and supported with density functional theory calculations. The crystal structure study revealed the presence of a pure single cubic spinel phase, where the unit-cell and the size were observed to decrease as the manganese incorporation was increased with clear indication of cationic redistribution and degree of inversion variations. Due to the very small variation of the total energy between different configurations, the probability of formation of a mixed phase was found to be very high in such a way that the more mixed was the phase, the more stable it was. A relevant fact was the noticed quasi-systematic ionic exchange made possible by the very short reaction times and high energy offered by the ultrasonic waves. For manganese concentrations up to 60%, the systematic ionic process started by incorporating manganese ions into octahedral sites and pushing iron ions to migrate and replace those of zinc in tetrahedral sites. Such an ionic movement was of central importance for the improvement of the magnetic properties due to the establishment of super-exchange interactions. Such an ionic engineering should definitely open the way to promising applications in biomedical imaging.

Characterization and performance of novel carbon-doped aluminum-modified bentonite for cost-effective fluoride removal

Elevated fluoride levels in water pose a critical global health issue, necessitating advanced remediation strategies. This study introduces a novel, cost-effective approach using clay minerals, specifically bentonite, enhanced with carbon-doped aluminum. The resulting composite, carbon-doped aluminum-bentonite (CCDAB), exhibits exceptional fluoride adsorption performance. Detailed structural analyses by SEM, FTIR, BET, and X-ray diffraction reveal successful carbon-doped aluminum integration, which markedly improves fluoride uptake. Adsorption kinetics adhere to pseudo-second-order models, signifying predominant chemical interactions, while the Langmuir isotherm model indicates monolayer coverage. CCDAB achieves a fluoride adsorption capacity of 85.51 mg/g and a removal efficiency of 95.3 %, demonstrating robust performance even in the presence of competing ions. Its efficacy over a broad pH range (3−7) is attributed to its high point of zero charge (pHpzc), which enhances electrostatic interactions. Carbon doping introduces additional active sites, synergistically enhancing fluoride removal alongside aluminum oxide. Thermodynamic analysis confirms that the process is both spontaneous and endothermic. The mechanisms of fluoride removal encompass electrostatic attraction, ion exchange, and surface complexation. This study highlights CCDAB’s promise as a highly effective and economical solution for fluoride contamination in water.