Specific Area Research Articles

Efficient removal of Cr6+ by magnetically modified biochar from aqueous solution:Removal mechanism investigation

The magnetic biochar is prepared by one-pot method using waste wooden building formwork as feedstock in the existence of the FeCl3 for Cr6+ removal form wastewater. Characterization analysis indicates that magnetic biochar exists Fe3O4 with specific surface area of the 333.89–496.35 m2/g, contributing to Cr6+ removal. Cr6+ removal process can be well analyzed by the Pseudo-second order and Hill models with adsorption capacity of 30.41 mg/g. The adsorption process analysis indicates that Cr6+ removal mechanism includes surface complexation, electrostatic attraction, reduction and pore filling. The influence of Fe2+ on Cr6+ removal is analyzed, indicating Fe2+ participation into Cr6+ removal by reduction. The magnetic biochar has excellent reusability after three cycles. The Cr6+ removal process is also investigated using column adsorption experiment, indicating that magnetic biochar has column adsorption amount of the 56.64 mg/g. The economic feasibility of the magnetic biochar is investigated and calculated with the production cost of $2.48/1kg. The waste wooden building formwork is converted into the efficient magnetic biochar for Cr6+ removal from wastewater.

Recent Advancements in the Development of Graphene‐Based Materials for Catalytic Applications

AbstractGraphene, a two‐dimensional material, presents unprecedented opportunities for catalytic applications, attributable to its unique planar structure, outstanding optical transmittance, superior electronic conductivity and mobility, extensive specific surface area, and elevated chemical stability, coupled with its tunability. In recent years, graphene‐based catalysts have garnered significant research attention and interest. This review aims to elucidate recent advancements in the synthesis of graphene‐based catalysts. It encompasses discussions on heteroatom‐doped metal‐free graphene catalysts, graphene composite catalysts (including graphene/metal and graphene/metal oxide composites), and their applications in various catalytic domains such as electrocatalysis, photocatalysis, and catalysis of organic reactions.

Metal-organic frameworks (MOFs) for photoreduction of CO2

In recent decades, human industrialisation has become increasingly advanced, and the quality of life has also improved. Subsequently, the excessive consumption of fossil fuels has caused a series of problems, for example, global environmental warming caused by excessive CO2 emissions. Among numerous CO2 reduction technologies, using solar energy as an energy source for the CO2 photoreduction is considered one of the most prospective technologies. This method not only reduces the amount of CO2, but also enables to converse CO2 into other valuable chemicals, thereby achieving carbon cycling. Metal-organic frameworks (MOFs) are composed of metal ions and organic ligands as three-dimensional porous materials. MOFs have many advantages, including sizeable specific surface area, excellent CO2 absorption capacity and modifiable pore structure, leading to broad application potential in photocatalytic reduction of CO2. This article mainly introduces three aspects: functionalisation and modification of pure MOFs, MOF-based composite materials, and MOF-derived materials, which further improve the CO2 photocatalytic efficiency of MOFs. Furthermore, it includes the analysis of reported examples, discussion and outlook on reaction mechanisms and challenges. At present, the main difficulties faced by MOFs-based photocatalysts lie in their economic feasibility and poor material stability. Therefore, this review aims to help stimulate in-depth research in this area as well as better exert the advantages of MOFs.

Investigating the properties and agronomic benefits of onion peel and chicken feather-derived biochars

Biochar production from unconventional biomass, specifically onion peel (OP) and chicken feathers (CF), was investigated in this study. Two distinct biochars were produced by doping each biomass with the other, with the aim of exploring the synergistic effects of different feedstock combinations on biochar properties. The biochar production process was conducted using a retort heating method and characterized using several techniques. A yield of 36 % was obtained for OP-doped biochar (OP92CF8-BC) and 23 % for CF-doped biochar (F92OP8-BC). Fourier Transform Infrared Spectroscopy analysis revealed characteristic functional groups from cellulose, hemicellulose, and lignin in OP92CF8-BC, while CF92OP8-BC displayed keratin-related peaks. Scanning Electron Microscopy imaging showed surface morphology differences, with OP92CF8-BC exhibiting a rougher and more porous structure compared to CF92OP8-BC. Energy-Dispersive X-ray Spectroscopy analysis confirmed the elemental composition, with OP92CF8-BC having higher carbon, calcium, and sulfur contents and CF92OP8-BC having higher nitrogen and oxygen contents. The biochar had specific surface areas of 342.4 and 200.80 m2/g for OP92CF8-BC and CF92OP8-BC, respectively. According to the results, using biochar treatments-more especially, CF92OP8-BC-can significantly enhance cob weight. This could be good for agricultural productivity. These findings highlight the influence of feedstock composition on the properties of biochar and provide insights for its potential applications in soil amendment and pollutant removal.

Pore evolution and reaction mechanism of coal under the combination of chemical activation and autothermal oxidation

Aiming at the limitation problems such as limited scope, high cost and energy consumption of coal bed penetration enhancement technology by traditional physical and chemical methods, a coal seam methane penetration enhancement method based on the combined action of chemical activation and auto thermal oxidation is proposed from the idea of utilizing the in-situ energy of the coal body. In this paper, N2 and CO2 adsorption, XPS and FTIR methods are used to study the pore structure evolution law and the change characteristics of the reactive structure of coal matrix under the effect of chemically activated autothermal oxidation. The synergistic microporous pore volume of chemical activation and auto thermal oxidation was 48.91 cm3/g−1 × 10-3, which was 28.96 % and 22.7 % higher than chemical activation and auto thermal oxidation respectively; The microporous specific surface area was 162.7 m2/g, which was 38 % and 26.6 % higher than chemical activation and auto thermal oxidation respectively. Activated coals expand and merge holes to a deeper degree after oxidative warming, and the complexity of the pore structure in the coal decreases; Highly reactive radicals in coal pores substantially promote the oxidation of coal structure, enhance the aromatic polymerization reaction of activated coal, and improve the maturity and aromaticity of activated coal, and the oxygen-containing functional groups in activated coal are negatively correlated with the oxidation temperature. The results of this study reveal the potential of the auto thermal oxidation-driven penetration enhancement method under chemical activation for coal seam gas penetration enhancement and extraction.

An Investigation into the Influence of Graphene Content on Achieving a High-Performance TiO2-Graphene Nanocomposite Supercapacitor.

This study presents the synthesis of TiO2-graphene nanocomposites with varying mass ratios of graphene (2.5, 5, 10, 20 wt. %) using a facile and cost-effective hydrothermal approach. By integrating TiO2 nanoparticles with graphene, a nanomaterial characterized by a two-dimensional structure, unique electrical conductivity and high specific surface area, the resulting hybrid material shows promise for application in supercapacitors. The nanocomposite specimens were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Raman microscopy, field-emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM). Additionally, supercapacitive properties were investigated using a three-electrode setup by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) tests. Notably, the TiO2-20 wt. % rGO nanocomposite exhibited the highest specific capacitance of 624 F/g at 2 A/g, showcasing superior electrochemical performance. This specimen indicated a high rate capability and cyclic stability (93 % retention after 2000 cycles). Its remarkable energy density and power density of this sample designate it as a strong contender for practical supercapacitor applications.

Defect formation and growth in metal nanocomposites consisting of Cu nanoparticles embedded in Ni or Al coatings

Fully inorganic or metallic nanocomposite coatings are promising materials for various applications but face limitations in term of their synthesis. A complementary synthesis process, Physical Vapor Deposition combined with magnetron sputtering and plasma-assisted gas-phase aggregation produced Cu nanoparticles embedded in metallic matrix. In this study, the effect of embedded nanoparticles on the matrix structure was investigated. Al and Ni were selected as matrix materials due to their different sputter yields leading to different growth modes film morphologies and difference in surface energy. Depending on the nanocomposite and deposition conditions, defects such as nodular growth were occasionally observed. These growth anomalies originated from the presence of nanoparticles creating new nucleation points for the matrix to grow disturbing the grain growth around it. Key factors responsible for their formation include the surface energy difference between the NPs and the matrix and the geometrical disruption occurring for large NP. In extreme cases with a high concentration of nanoparticles, coatings entirely constituted of nodular defects were produced which can be advantageous for applications needing large specific surface area.

The directions of enhanced activated carbon fibers for iodine capture from humid gas streams: Synergistic mechanisms of microporosity, hydrophobicity, and nitrogen sites

Activated carbon fiber (ACF) is widely used as a critical adsorbent for removing gaseous radioiodine produced during spent fuel reprocessing. However, conventional ACF exhibits a broad pore distribution and high moisture affinity, significantly diminishing their effectiveness in capturing iodine under humid conditions. In this study, we endowed bare ACF with the dual functions of preferentially I2-matched pores (93.62 % microporosity) and hydrophobicity (water contact angle of 132.1°) using a facile method of depositing polydivinylbenzene (PDVB) nanoparticles, overcoming the limitations of traditional modification methods that have a single target. We successfully prepared amine-functionalized hydrophobic ACF (ACF-PDA@PDVB-HMTA) with a high specific surface area (1392 m2/g) by introducing iodine-affinity reactive groups (NH2, CN, and OH). ACF-PDA@PDVB-HMTA exhibited a groundbreaking static adsorption capacity of 1886 ± 56 mg/g for I2 at 96 % relative humidity. Notably, its dynamic iodine adsorption on iodine-water vapor mixed stream was 1873.78 mg/g, which is 66.31 % higher than that of the original ACF (1126.7 mg/g) at real-life conditions of 75 °C and 50 % relative humidity, underscoring the synergistic “1 + 1 + 1 = 3” effect of the three mechanisms. The scalable application of the spray-deposited PDVB approach to other porous carbon materials also yielded exemplary modification results. This synergistic strategy provides a promising solution for improving the overall I2 capture.

Advanced MXene materials: Paving the way for next-generation lithium-sulfur batteries in energy storage

In recent years, lithium-sulfur (Li-S) batteries, with high theoretical energy density and low cost, have become one of the most promising energy storage systems. However, the insulation of sulfur, the "shuttle effect" of polysulfides and volume expansion hinder their practical applications. MXenes have excellent electrical conductivity, high specific surface area, and a strong adsorption capacity for polysulfides, which helps to overcome the shortcomings of traditional Li-S batteries. In this paper, the structure, properties and preparation methods of MXenes are reviewed, and the applications of MXenes in the cathode, separator and anode of Li-S batteries are introduced. Finally, the future directions of MXenes in the field of Li-S batteries are prospected.

One-step synthesis of double-walled NiCo2O4 hollow nanotubes using hollow fiber templates created by airflow-coaxial electrospinning

Metal oxide electrode material NiCo2O4 has significant potential for application as an Electrode material due to its excellent electrochemical performance and environmentally friendly characteristics. This paper utilizes a unique airflow-coaxial electrospinning technique combined with a simple one-step solution reaction to prepare NiCo2O4 nanotubes with a complex double-walled hollow structure. The XPS and XRD results demonstrated the synthesis of the NiCo2O4 materials, while the SEM and TEM results verified the presence of a double-walled hollow structure in the NiCo2O4 nanotubes. The electrochemical performance of the NiCo2O4 double-walled hollow nanotubes is significantly improved compared to those single-layer hollow nanotubes. The maximum specific capacitance of those two kinds of nanotubes is 437.5 F/g and 336.7 F/g under the current density of 1 A/g, respectively. The origin of the electrochemical performance improvement can be attributed to the increased specific surface area and the presence of interlayer ion transport channels in the double-walled hollow structure. The study is very helpful in improving the application prospect of NiCo2O4 material as the electrode material of supercapacitors. Equally important, this study also presents an efficient method to fabricate double-walled hollow nanostructures based on special templates.

Enhanced catalytic performance and antichlorine poisoning over Cu-doped cobalt oxide nanosheets for chlorobenzene oxidation

The degradation of Chlorinated volatile organic compounds (CVOCs) by catalytic oxidation forms toxic products, and catalysts may be poisoned by chlorine at low temperatures. To address this, a Cu-assisted strategy is proposed for enhancing the catalytic degradation of chlorobenzene (CB) over cobalt oxide nanosheets. The Cu-doped Co3O4 catalysts exhibited lower T90 values (temperatures with 90 % conversion) and improved stability compared to the unmodified catalyst. These results were attributed to strong metal-metal interactions between Cu species and cobalt oxide nanosheets, which showed a high specific surface area, reduced binding energy of lattice oxygen, higher surface oxygen concentration, and more surface Co3+ species. These properties promoted low-temperature catalytic activity. In addition, the disappearance of Cu2+ satellite peak after the catalyst is used, indicating that the Cu2+ also contributes to the catalytic activity. Furthermore, the in situ FTIR spectra provided details about the reaction mechanism of CB degradation over Cu-doped cobalt oxide nanosheets. The oxygen vacancy generation and the surface absorption of chlorine-containing intermediates were calculated using density functional theory calculations. This study provides new insight into novel pathways for catalyst design aimed at CB degradation.

Ambient Synthesis of Vanadium-based Prussian Blue Analogues Nanocubes for High-performance and Durable Aqueous Zinc-ion Batteries with Eutectic Electrolytes.

Prussian blue analogues (PBAs) have been widely studied in aqueous zinc-ion batteries (AZIBs) due to the characteristics of large specific surface area, open aperture, and straightforward synthesis. In this work, vanadium-based PBA nanocubes were firstly prepared using a mild in-situ conversion strategy at room temperature without the protection of noble gas. Benefiting from the multiple-redox active sites of V3+/V4+, V4+/V5+ and Fe2+/Fe3+, the cathode exhibited an excellent discharge specific capacity of 200 mA h g-1 in AZIBs, which is much higher than those of other metal-based PBAs nanocubes. To further improve the long-term cycling stability of the V-PBA cathode, a high concentration water-in-salt electrolyte (4.5 M ZnSO4 + 3 M Zn(OTf)2), and a water-based eutectic electrolyte (5.55 M glucose + 3 M Zn(OTf)2) were designed to successfully inhibit the dissolution of vanadium and improve the deposition of Zn2+ onto the zinc anode. More importantly, the assembled AZIBs maintained 55% of their highest discharge specific capacity even after 10000 cycles at 10 A g-1 with superior rate capability. This study provides a new strategy for the preparation of pure PBA nanostructures and a new direction for enhancing the long-term cycling stability of PBA-based AZIBs at high current densities for industrialization prospects.

Influence of preparative parameters on the morphology and reactivity of synthetic hexagonal birnessite

Birnessite is a phyllomangante mineral widely found in surficial environments. Its morphology not only affects its adsorption and oxidation properties but also indicate changes in the climatic conditions of ancient Earth. This study explored how preparative parameters affect the morphology and reactivity birnessite. Synthesized at boiling temperatures, birnessite nanoflowers measured 265 nm with a specific surface area (SSA) of 34.87 m2/g, while at 65 °C, they increase to 2251 nm with a similar SSA of 30.33 m2/g. Lowering KMnO4 or HCl concentrations increased nanoflower size. Reduced concentration of KMnO4 hindered Coulombic forces, fostering a parallel petal arrangement and a higher SSA (59.11 m2/g). Lower concentration of HCl led to perpendicular petals and a reduced SSA (12.33 m2/g). Decreased concentrations of both KMnO4 and HCl reduced initial δ-MnO2 concentration, allowing time for edge-to-edge assembly and nanoflake substrate formation. Subsequently, δ-MnO2 vertically assembled on substrates to form microwalls with SSA of 85.39 m2/g. Organic acids as capping agents disrupted this assembly. Adsorption tests for Cd2+ revealed microwalls achieved 7102 mmol/kg, surpassing original birnessite nanoflowers at 2114 mmol/kg. These results provide insights into the crystallization processes and reactivity of natural birnessite, as well as methods for the controllable synthesis of nanoflowers.

Enhanced Low‐Temperature Oxidation Activity of Cu‐Doped Highly Active Pd‐Based Catalysts

Pd‐based catalysts supported on cerium‐zirconium (CZ) oxygen storage materials (OSM) have emerged as promising candidates for the catalytic oxidation of CH4 and CO. However, achieving efficient and stable treatment of CH4 and CO in exhaust gases with Pd‐based catalysts remains a long‐term challenge. To address this, we propose a straightforward strategy of doping the supports with Cu to enhance the catalytic performance of Pd/Ce0.4Zr0.5La0.1O1.95 catalysts. Performance tests revealed that the catalytic activity of the Cu‐doped catalysts significantly improved, with T90 (CH4) decreasing from 418 to 301 ℃ and T90 (CO) decreasing from 141 to 113 ℃. Notably, the copper‐doped catalysts exhibited enhanced water and sulfur resistance while maintaining excellent thermal stability. The CO conversion decreased by less than 2% after a thermal deactivation experiment lasting over 100 hours. The reduction in particle size and the increase in specific surface area due to copper doping are key factors contributing to the improved total oxygen storage capacity (OSC). The main reasons for the increase in total OSC are likely the reduced particle size and increased specific surface area.

Sustainable 3D-printed cellulose-based biocomposites and bio-nano-composites: Analysis of dielectric performances

The development of cellulose-reinforced biomaterials appears to be an attractive approach for the production of sustainable materials with good mechanical properties. Although 3D printing of cellulose-reinforced biomaterials has become popular, there is very little feedback regarding their use in electrical insulation applications. This study aims to propose bio-nano-composites containing polylactic acid (PLA), microcrystalline (MCC) and nanocrystalline (NCC) cellulose by fused filament fabrication (FFF) for electrical insulation applications. The influence of the 3D printing process, cellulose content and filler size on dielectric properties was investigated. The addition of cellulosic fillers, and considering their high polarity, increased the dielectric constant (ε'), dielectric loss (ε''), as well as the AC electrical conductivity (σAC) of the composites. Cellulosic fillers also increased the crystallization rate of the materials. At equivalent content, the highest polarization potential were observed for NCC-based composites and were attributed to the nanofiller's better dispersion and available specific surface area. Finally, the 3D printing process affects all the measured properties, due to a combined effect (lower crystalline content and voids presence). The porosity rate was measured at 2.5 % for the neat PLA and increased progressively from 3.1 % to 5.8 % for the cellulose-based composites. These findings showed the benefits provided by the FFF technology in the production of cellulose-based biocomposites with good electrical insulation properties, while noting some needed feedback on the thermomechanical properties of such materials.

Modulating porosity and hydrophilicity of granular adsorbent by water-soluble polymers to enhance lithium extraction from ultrahigh Mg/Li ratio brine

The development of granular adsorbents with high adsorption capability and high cycle stability is of great significance for the application in efficiently extracting lithium from salt lake brine. Herein, the structure of granular aluminum-based adsorbents was regulated by adding water-soluble polymer PEG. The results showed that the molecular weight of PEG was closely related to the pore structure and surface hydrophilicity of the granular adsorbents. With the decrease of the molecular weight of PEG, the specific surface area, the average surface pore size, and the hydrophilicity of granular adsorbents increase. The optimized adsorbent PSF-PEG600@AD formed a complex pore structure with surface macropores and internal mesopores as well as excellent hydrophilicity. The mechanical strength and wear resistance are enhanced. This unique porous structure and surface hydrophilicity enable PSF-PEG600@AD rapid adsorption equilibrium in the old brine of Qarhan salt lake with a Mg/Li ratio of 323 within 4 h. The adsorption capacity remains as high as 99.02 % after 10 static adsorption-desorption cycles, showing excellent cyclic stability. This study guides a direction in preparing high-performance granular adsorbents with adjustable pore structure and surface properties.

Synthesis of mesoporous γ-alumina from a low-grade boehmite ore: Effect of thermal/chemical processing order on physico-chemical characteristics of adsorbent and regeneration of used transformer oils

Mesoporous γ-alumina adsorbents were synthesized from a low-grade boehmite ore, using the heat-treatment/acid-leaching (TC) and vice-versa (CT), under 400–600℃, 2–6 M HCl and H2SO4 solutions. The crystallinity of active species, morphology, elemental mapping, specific surface area, gravimetric phase changes, and chemical composition of the samples were characterized. The 0.50–1.00 mm γ-alumina prepared through heating, and followed by acid leaching with HCl (TC sample) presented mesoporous structure with the highest specific surface area of 245.802m2/g, pore volume 0.32773cm3/g, and average pore diameter of 44.3420A0. Using both CT and TC adsorbents, along with a commercial adsorbent, for the regeneration of used transformer oil, the TC adsorbent demonstrated the best performance, resulting in improved oil properties such as viscosity, interfacial tension, total acid number, dielectric dissipation factor, resistivity, and moisture content. Furthermore, the TC adsorbent was affected less by surface attrition and producing fine debris during recovery of oil compared to the commercial one.

Application of Mesoporous Carbon-Based Highly Dispersed K-O2 Strong Lewis Base in the Efficient Catalysis of Methanol and Ethylene Carbonate.

As an atom-economical reaction, the direct generation of dimethyl carbonate (DMC) and ethylene glycol (EG) via the transesterification of CH3OH and ethylene carbonate (EC) has several promising applications, but the exploration of carriers with high specific surface areas and novel heterogeneous catalysts with more basic sites remains a long-standing research challenge. For this purpose, herein, a nitrogen-doped mesoporous carbon (NMC, 439 m2/g) based K-O2 Lewis base catalyst (K-O2/NMC) with well-dispersed strongly basic sites (2.23 mmol/g, 84.5%) was designed and synthesized. The compositions and structures of NMC and K-O2/NMC were comprehensively investigated via Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, N2 adsorption-desorption, CO2 temperature-programmed desorption, and contact angle measurements. The optimal structural configuration and electron cloud distribution of the K-O2/NMC catalyst were simulated using first-principles calculations. The electron transfer predominantly manifested as a flow from K-O to C-O/C-N, and the interatomic interactions between each atom were enhanced and exhibited a tendency for a more stable state after redistribution. Furthermore, the adsorption energies (Eads) of CH3OH at K-O-O and K-O-N sites were -1.4185 eV and -1.3377 eV, respectively, and the O atom in CH3OH exhibited a stronger adsorption tendency for the K atom at the K-O-O site. Under the optimal conditions, the EC conversion, DMC/EG selectivity, and turnover number/frequency were 80.9%, 98.6%/99.4%, and 40.5/60.8 h-1, respectively, with a reaction rate constant (k) of 0.1005 mol/(L·min). Results showed that the heterogeneous K-O2/NMC catalyst prepared herein greatly reduced the reaction cost while guaranteeing the catalytic effect, and the whole system required a lower reaction temperature (65 °C), a shorter reaction time (40 min), and a lower catalyst amount (2.0 wt % of EC). Therefore, K-O2/NMC can be used as a catalyst in different transesterification reactions.

The effect of silicon dioxide on the structural, thermal and transport properties of an organic ionic plastic crystal (n-C4H9)4NBF4

Composite solid electrolytes based on an organic ionic plastic crystal (n-C4H9)4NBF4 with highly dispersed SiO2 with specific surface area of Ss = 324±10 m2/g have been studied for the first time. By methods of X-ray diffraction and differential scanning calorimetry, it was found that the introduction of SiO2 leads to amorphization of the salt. An unusual size effect was observed in the composites: the temperature of the polymorphic transition of the salt shifted from 67 °C to 60 °C, while the melting point did not change. The 0.15(n-C4H9)4NBF4–0.85SiO2 composite was found to possess the highest electrical conductivity (σ = 2∙10–5 S/cm at 150 °C), which is 1.5 orders of magnitude higher than that of the initial salt. Modelling of the concentration dependences of the electrical conductivity of composites using the mixing equation showed that the reason for the increase in electrical conductivity is the formation of an amorphous layer of salt, the electrical conductivity of which is 3 orders of magnitude higher than that of the crystalline phase (n-C4H9)4NBF4. The obtained results can be used for the design of high-performance composites based on organic ionic plastic crystals for application in electrochemical devices.

Highly porous P(DVB-AMPS) copolymer with tailored surface engineering for efficient fluoride capture from water

Surface engineering, especially surface hydrophilicity and active binding sites are crucial for porous polymers in the removal of fluoride ions from water. Herein, a novel P(DVB-AMPS) copolymer with tailored surface engineering was designed through a one-step polymerization method by incorporating diethylene-benzene (DVB) and 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS). AMPS endows abundant active binding sites and provides P(DVB-AMPS) with both hydrophilicity and affinity for fluoride ions, while the monomer DVB acting as a crosslinker, facilitating pore generating. The surface hydrophilicity of P(DVB-AMPS) could be easily tuned by increasing the amounts of AMPS with the contact angle decreased from 126° (PDVB) to 52°. Furthermore, P(DVB-AMPS) material maintains a large specific surface area of 428 m2 · g[Formula: see text] and preserves its highly porous structure. P(DVB-AMPS) exhibits an efficient adsorption capacity (51.9 mg · g[Formula: see text]) and a rapid adsorption rate (6.83 mg · g[Formula: see text] · min[Formula: see text]), which demonstrates competitive performance compared with previous reports. Importantly, the material possesses highly selective adsorption toward fluoride. The excellent adsorption performance of P(DVB-AMPS) is attributed to the high porosity, improved surface hydrophilicity and active binding sites. This work not only provides a new strategy for designing high-performance adsorbents but also offers a novel polymer material for the efficient capture of fluoride ions from water.