Tunable Pore Structure Research Articles

Redox Synergy: Enhancing Gas Sensing Stability in 2D Conjugated Metal-Organic Frameworks via Balancing Metal Node and Ligand Reactivity.

Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have emerged as promising candidates in gas sensing, owing to their tunable porous structure and conductivity. Nevertheless, the reported gas sensing mechanisms heavily relied on electron transfer between metal nodes and gas molecules. Normally, the strong interaction between the metal sites and target gas molecule would result poor recovery and thus bad recycling property. Herein, we propose a redox synergy strategy to overcome this issue by balancing the reactivity of metal sites and ligands. A 2D c-MOF, Zn3(HHTQ)2, was prepared for nitrogen dioxide (NO2) sensing, which was constructed from active ligands (hexahydroxyltricycloquinazoline, HHTQ) and inactive transition-metal ions (Zn2+). Substantial characterizations and theoretical calculations demonstrated that by utilizing only the redox interactions between ligands and NO2, not only high sensitivity and selectivity, but also excellent cycling stability in NO2 sensing could be achieved. In contrast, control experiments employing isostructural 2D c-MOFs with Cu/Ni metal nodes exhibited irreversible NO2 sensing. Our current work provides a new design strategy for gas sensing materials, emphasizing harnessing the redox activity of only ligands to enhance the stability of MOF sensing materials.

Efficient adsorption of pesticides by porous organic polymers based on imine/aminal linkages

Porous organic polymers (POPs) are promising materials for pesticide adsorption from wastewater due to their high surface area and tunable porous structure. MPT-TPA-POPs were synthesized in green solvents using inexpensive diamines and dialdehyde monomers to form imine and aminal linkages. This study investigated for the first time the adsorption and removal effects of pesticides Forchlorfenuron (CPPU) and Acetamiprid (ACE) using MPA-TPA-POPs adsorbent. FTIR, SEM, EDS, BET, and XPS analyses were utilized to examine changes in functional groups, morphology, elemental composition, specific surface area, and pore volume of MPT-TPA-POPs before and after CPPU and ACE adsorption. At an initial concentration of 50 mg/L, with a dosage of 0.5 g/L, a pH of 7, a temperature of 298 K, and an adsorption time of 120 min, the maximum removal rates for CPPU and ACE are achieved at 99.94 % and 68.44 %, respectively. The quasi-second-order kinetic and Langmuir isotherm model were deemed more appropriate for accurately describing this adsorption process. Thermodynamically, the adsorption process was observed to be spontaneous and exothermic. Simultaneously, during cyclic adsorption-desorption experiments, the adsorption capacity of MPT-TPA-POPs material showed no significant decline even after six cycles. The findings of this research suggest that MPT-TPA-POPs can act as a green, eco-friendly, cost-efficient, and effective adsorbent for eliminating CPPU and ACE pesticides from water, offering an economically feasible approach to pesticide removal.

Enhanced Hydrogen Peroxide Decomposition in a Continuous-Flow Reactor over Immobilized Catalase with PAES-C.

Due to the specificity, high efficiency, and gentleness of enzyme catalysis, the industrial utilization of enzymes has attracted more and more attention. Immobilized enzymes can be recovered/recycled easily compared to their free forms. The primary benefit of immobilization is protection of the enzymes from harsh environmental conditions (e.g., elevated temperatures, extreme pH values, etc.). In this paper, catalase was successfully immobilized in a poly(aryl ether sulfone) carrier (PAES-C) with tunable pore structure as well as carboxylic acid side chains. Moreover, immobilization factors like temperature, time, and free-enzyme dosage were optimized to maximize the value of the carrier and enzyme. Compared with free enzyme, the immobilized-enzyme exhibited higher enzymatic activity (188.75 U g-1, at 30 °C and pH 7) and better thermal stability (at 60 °C). The adsorption capacity of enzyme protein per unit mass carrier was 4.685 mg. Hydrogen peroxide decomposition carried out in a continuous-flow reactor was selected as a model reaction to investigate the performance of immobilized catalase. Immobilized-enzymes showed a higher conversion rate (90% at 8 mL/min, 1 h and 0.2 g) compared to intermittent operation. In addition, PAES-C has been synthesized using dichlorodiphenyl sulfone and the renewable resource bisphenolic acid, which meets the requirements of green chemistry. These results suggest that PAES-C as a carrier for immobilized catalase could improve the catalytic activity and stability of catalase, simplify the separation of enzymes, and exhibit good stability and reusability.

In situ semi-etching of bimetallic LDH nanosheet arrays into FeNi-LDH/MOF to boost oxygen evolution reaction

The inherent sluggish kinetics of water oxidation is the core issue for electrochemical hydrogen production from water splitting. Metal organic frameworks (MOFs) with tunable porous structures, abundant coordination metal centers and large specific surface area are expected as efficient electrocatalysts. In this paper, FeNi-LDH/MOF composite nanostructures were successfully constructed on carbon cloth (CC) through partially converting iron-nickel layered double hydroxide (FeNi-LDH) into FeNi-MOF (NiFe(CN)5NO) by an in-situ semi-etching method. The MOF nanocrystals in this material are in-situ decorated on the surface of FeNi-LDH nanosheets, providing abundant open active sites and mass transfer channels for electrocatalysis. Thanks to the synergistic effect of the LDH and MOF, as well as the exceptional hierarchical architecture, the FeNi-LDH/MOF/CC as a self-supported electrode exhibits distinguished electrocatalytic OER performance, with a low overpotential of 263 mV@100 mA cm−2 and a small Tafel slope of 50.2 mV dec-1 in 1.0 M KOH. In addition, the catalyst exhibits good durability with almost constant current density during 24 h OER test. This work provides an effective way to design high-performance MOFs-based composite electrocatalytic materials.

Construction of 2D MOF nanosheets with missing-linker defects for enhanced supercapacitor performance

Metal-Organic Frameworks (MOFs) are highly promising as electrode materials for supercapacitor development due to their large specific surface areas and tunable pore structures. Nevertheless, the intrinsic poor conductivity and suboptimal electrochemical performance of MOFs present substantial challenges. Traditional pyrolysis methods often compromise the inherent characteristics of MOFs. Consequently, a reasonable design of the original MOFs is a promising approach to enhancing its performance. This study commenced with pristine two-dimensional (2D) Ni-BTC (BTC = Trimesic acid) and improved their electrical conductivity and active site accessibility by embedding isophthalic acid (IPA) as missing linkers, resulting in defective Ni-BTC/IPA-x. The physicochemical properties of Ni-BTC/IPA were systematically characterized. The results indicate that defects effectively modulate the electronic structure of the metal center, pore structures, and specific surface areas of MOFs, which is conducive to improving supercapacitor performance. Electrochemical measurements reveal that Ni-BTC/IPA-3 exhibits an exceptional specific capacity of 1209 F g−1 at 0.5 A g−1, demonstrating a rate performance of 70.8 %. Furthermore, hybrid supercapacitor (HSC) devices, incorporating the Ni-BTC/IPA-3, possess an energy density of 30 Wh kg−1 at a power density of 1775.8 W kg−1. These HSC devices successfully power multi-colored light-emitting diodes (LEDs), highlighting their significant potential for practical energy storage applications.

Recent progress of covalent organic frameworks in high selective separation of radionuclides

The utilization of nuclear energy power and nuclear weapon tests not only releases large amounts of radionuclides into environment, but also needs 235U as nuclear fuel for nuclear energy generation. Covalent organic frameworks (COFs) have the advantages of tunable porous structures, adjustable active sites and enough special functional groups, which assure the high selective preconcentration of target radionuclides from complex solutions. In this perspective, the selective extraction of radionuclides (U(VI) as representative cationic ion, Tc(VII) as representative anionic ion, I2 as gaseous nuclide and other nuclides) by COFs through sorption, and photocatalytic strategies are described, and the results show the high efficiency of COFs in target radionuclides removal. The perspective and challenges for the real applications of COFs in future are discussed in the end.Graphical

Versatile filter membrane for effective sampling and real-time quantitative detection of airborne pathogens

Construction of air filter membranes bearing prominent collecting and transferring capability is highly desirable for detecting airborne pathogens but remains challenging. Here, a hyaluronic acid air filter membrane (HAFM) with tunable heterogeneous micro-nano porous structures is straightforwardly constructed through the ethanol-induced phase separation strategy. Airborne pathogens can be trapped and collected by HAFM with high performance due to the ideal trade-off between removal efficiency and pressure drop. By exempting the sample elution and extraction processes, the HAFM after filtration sampling can not only directly disperse on the agar plate for colony culture but also turn to an aqueous solution for centrifugal enrichment, which significantly reduces the damage and losses of the captured microorganisms. The following combination with ATP bioluminescence endows the HAFM with a real-time quantitative detection function for the captured airborne pathogens. Benefiting from high-efficiency sampling and non-traumatic transfer of airborne pathogens, the real-world bioaerosol concentration can be facilely evaluated by the HAFM-based ATP assay. This work thus not only provides a feasible strategy to fabricate air filter membranes for efficient microbial collection and enrichment but also sheds light on designing advanced protocols for real-time detection of bioaerosols in the field.

Adsorption studies of tetracycline hydrochloride and diclofenac sodium on NH2-MIL-53(Al/Zr) sodium alginate gel spheres

Metal-organic frameworks are emerging inorganic-organic hybrid materials that can be self-assembled from metal ions and organic ligands via coordination bonds. These materials possess large specific surface area, tunable pore structure, abundant active center, diversity of functional groups as well as high mechanical and thermal stability which promote their applications in adsorption and catalysis studies. In this study, NH2-MIL-53(Al/Zr) was prepared and embedded into sodium alginate gel spheres (NH2-MIL-53(Al/Zr)-SA) and its adsorption properties towards TC and DCF in solution were investigated. According to XRD and FTIR analysis, the structure of the raw material was not changed after making the gel spheres. The maximum adsorption towards TC (pH =3) and DCF (pH =5) reached 98.5 mg·g−1 and 192 mg·g−1, respectively. The process was consistent with Langmuir and Freundlich, suggesting that there was both monolayer and multilayer adsorption which infers the presence of physical adsorption (intra-particle diffusion) and non-homogeneous chemical adsorption. The thermodynamic parameters showed that the adsorption process was a spontaneous entropy increasing reaction. The regeneration rate of spent NH2-MIL-53(Al/Zr)-SA could still reach 99.1 % after three cycles, indicating good regeneration performance. This study can provide a basis for the application of NH2-MIL-53(Al/Zr)-SA in wastewater treatment.

Preparation of tomato peel pomace powder/polylactic acid foams under supercritical CO2 conditions: Improvements in cell structure and foaming behavior

Polylactic acid (PLA) is an eco-friendly material that can help address the problems of petroleum depletion and pollution. Blending renewable biomass materials with PLA to create composite foams with a tunable pore structure, superior performance, and low cost is a green technique for improving the pore structure and mechanical characteristics of single PLA foams. PLA/TP composites were created using melted tomato peel pomace powder (TP), which has a lamellar structure, as a reinforcing agent. Then, the relationship between the vesicle structure, morphology, and properties of the PLA/TP composite foams produced through supercritical CO2 intermittent foaming were investigated. The findings revealed that TP considerably enhanced the rheological characteristics and crystalline behavior of PLA. The PLA/TP composite foam had a better cell structure, compression characteristics, and wettability than pure PLA. The expansion ratio of the PLA/TP composite could reach 18.8, and its thermal conductivity decreased from 174.2 mW/m·K at 100 °C to 57.8 mW/m·K at 120 °C. Furthermore, annealing before foaming decreased the average composite foam blister size from 110.09 to 66.53 μm, and the annealing process also improved compression performance. This study contributes to solving environmental difficulties and creating PLA foams with controlled bubble structures, uniform bubble sizes, and outstanding overall performance.

Large-scale and facile fabrication of phenyl-containing silicone foam materials with lightweight, wide-temperature flexibility and tunable pore structure for exceptional thermal insulation

Silicone foam materials with unique inorganic/organic molecular networks and porous structures are widely used in many emerging fields from aerospace to new energy fields. However, current silicone foam materials still show some limitations, such as the relatively high-density values of >200 mg cm−3, complex fabricating process and difficulty in tailoring pore structure. Herein, we report a large-scale and facile fabricating strategy to prepare phenyl-containing silicone foam materials (PhSiRF) with ultra-lightweight feature, tunable pore structure, and excellent wide-temperature mechanical flexibility. Interestingly, the presence of phenyl groups onto the Si–O–Si backbone tailors the chemical foaming rate probably due to the steric hindrance effect, thus producing tunable pore size distributions in the range of 180–500 μm. Typically, the PhSiRF with 50 % phenyl groups not only shows a very low density of ∼100 mg cm−3, superior to previous silicone foams and composites, but also exhibits wide-temperature flexibility (stable compressive strain of 80 % from −90 to 210 °C) and excellent thermal insulation performance, which outperforms those of conventional polymer foams including polyurethane, polyethylene and melamine foams. Based on the structure observation and theory analysis, the influence of different pore morphological structures on the thermal insulation performance is discussed and demonstrated. Clearly, this work provides a new yet simple method for developing high-performance silicone rubber foam materials for promising thermal insulation applications.

Bimetallic Metal Sites in Metal-Organic Frameworks Facilitate the Production of 1-Butene from Electrosynthesized Ethylene.

Converting CO2 to synthetic hydrocarbon fuels is of increasing interest. In light of progress in electrified CO2 to ethylene, we explored routes to dimerize to 1-butene, an olefin that can serve as a building block to ethylene longer-chain alkanes. With goal of selective and active dimerization, we investigate a series of metal-organic frameworks having bimetallic catalytic sites. We find that the tunable pore structure enables optimization of selectivity and that periodic pore channels enhance activity. In a tandem system for the conversion of CO2 to 1-C4H8, wherein the outlet cathodic gas from a CO2-to-C2H4 electrolyzer is fed directly (via a dehumidification stage) into the C2H4 dimerizer, we study the highest-performing MOF found herein: M' = Ru and M″ = Ni in the bimetallic two-dimensional M'2(OAc)4M″(CN)4 MOF. We report a 1-C4H8 production rate of 1.3 mol gcat-1 h-1 and a C2H4 conversion of 97%. From these experimental data, we project an estimated cradle-to-gate carbon intensity of -2.1 kg-CO2e/kg-1-C4H8 when CO2 is supplied from direct air capture and when the required energy is supplied by electricity having the carbon intensity of wind.

Fabrication of lignosulfonate-derived porous carbon via pH-tunable self-assembly strategy for efficient atrazine removal

Herein, a straightforward protocol was developed for the one-pot synthesis of N-doped lignosulfonate-derived carbons (NLDCs) with a tunable porous structure using natural amino acids-templated self-assembly strategy. Specifically, histidine was employed as a template reagent, leading to the preparation of 10-NLDC-21 with remarkable characteristics, including the large specific surface area (SBET = 1844.5 m2/g), pore volume (Vmes = 1.22 cm3/g) and efficient adsorption for atrazine (ATZ) removal. The adsorption behavior of ATZ by NLDCs followed the Langmuir and pseudo-second-order models, suggesting a monolayer chemisorption nature of ATZ adsorption with the maximum adsorption capacity reached up to 265.77 mg/g. Furthermore, NLDCs exhibited excellent environmental adaptability and recycling performance. The robust affinity could be attributed to multi-interactions including pore filling, electrostatic attraction, hydrogen bonding and π-π stacking between the adsorbents and ATZ molecules. This approach offers a practical method for exploring innovative bio-carbon materials for sewage treatment.

Direct activation and hydrophobic modification of biomass-derived hierarchical porous carbon for toluene adsorption under high humidity

Hierarchical porous starch-based carbon (PSC) with tunable pore structure (surface area 1974 ∼ 2721 m2/g and pore volume 0.80 ∼ 1.74 cm3/g) was prepared through direct activation. Due to its high surface area and large pore volume, PSC shows great potential for volatile organic compounds (VOCs) removal. Water vapor commonly exists along with VOCs and the competitive adsorption between VOCs and water vapor would significantly restrict the VOCs adsorption of PSC under high humidity. To address this issue, hydrophobic porous starch-based carbon composite (PSCC) was also prepared by physically mixing PSC with poly-divinylbenzene (PDVB) for toluene adsorption under high humidity to suppress the influence of water vapor. As relative humidity increased from 0 % to 80 %, the toluene adsorption capacity of PSC-2 decreased by 46 % while PSCC only experienced a decrease of 22 %. PSCC could also maintain its toluene adsorption performance (close to 100 %) after five adsorption–desorption cycles. Theoretical computations were also proved that the addition of PDVB inhibits water vapor adsorption and promotes its desorption, thereby enhancing the toluene adsorption of PSCC under high humidity. This work provides a controllable preparation and facile modification of porous carbon to improve its toluene adsorption under high humidity, offering a great application prospect for VOCs removal.

Preferential Formation of Ethylene via Electrocatalytic CO2 Reduction on Mesoporous Cu2O Nanoparticles: Synergistic Effects of Pore Structure Confinement and Surface Amine

Comprehensive SummaryWe present a facile synthetic strategy to create mesoporous Cu2O nanocrystals with tunable pore structures and surface functional groups of amine derivatives for efficient and preferable electrochemical conversion of CO2 into ethylene. The structural characteristics of these Cu2O nanocrystals can be manipulated using a set of amine derivatives, such as pyridine, 4,4'‐bipyridine, and hexamethylenetetramine, during the oxidative etching process of Cu nanocrystals by bubbling gaseous oxygen in N,N‐dimethylformamide solution. These amine derivatives not only serve as surface functional groups but also significantly affect the resulting pore structures. The synergistic effect of pore structure confinement and surface amine functionalization leads to the superb Faradaic efficiency (FE) of 51.9% for C2H4, respectively, together with the C2H4 partial current density of –209.4 mA·cm−2 at –0.8 V vs. reversible hydrogen electrode (RHE). The relatively high selectivity towards C2H4 was investigated using DFT simulations, where 4,4'‐bipyridine functionalized Cu2O seemed to favor the C2H4 formation with the low free energy of the intermediates. This study provides a feasible strategy to manipulate the pore structure and surface functionalization of mesoporous Cu2O nanocrystals by regulating the oxidative etching process, which sheds light on the rational preparation of high‐performance CO2RR electrocatalysts.

Enhancing Efficiency and Stability in Carbon-Based Perovskite Solar Cells by Double Passivation with Ultralow-Cost Coal-Derived Graphene and Its Derivatives.

Coal-derived carbon nanomaterials possess numerous superior features compared to other classic carbon, such as readily accessible surfaces, tunable pore structure, and facile and precise surface functionalization. Therefore, the controllable preparation of coal-derived carbon nanomaterials is anticipated to be of great significance for the performance improvement and commercialization process of carbon-based perovskite solar cells (C-PSCs). In this study, we successfully synthesized highly stable and commercially valuable graphene oxide (GO) and reduced graphene oxide (rGO) utilizing coal. Compared to traditional methods and commercial graphene, the chemical oxidation and pyrolysis process used in this study is mild and simple, offering the advantages of controlled composition and the absence of other impurities. GO or rGO was incorporated into the top of the SnO2 electron transport layer (ETL) of C-PSCs. Under optimized conditions and ultraviolet-ozone (UVO) irradiation, the ultimate power conversion efficiency (PCE) increased from the unmodified 12.4 to 14.04% (based on rGO) and 15.18% (based on GO), representing improvements of 22 and 31%, respectively. The improved photovoltaic performance is mainly owing to enhanced charge transport capabilities, denser interfacial contacts, improved carrier separation properties, increased conductivity, and abundance of hydrophilic functional groups in GO, which can form more stable hydrogen bonds with SnO2. After being stored at room temperature and ambient humidity for 30 days, the modified, unpacked devices retained 87% of the highest power conversion efficiency (PCE). This study introduces a practical and manageable method to enhance the performance of C-PSCs by using functional carbon nanomaterials derived from coal.

Vapor-induced phase-separation-enabled versatile direct ink writing

Versatile printing of polymers, metals, and composites always calls for simple, economic approaches. Here we present an approach to three-dimensional (3D) printing of polymeric, metallic, and composite materials at room conditions, based on the polymeric vapor-induced phase separation (VIPS) process. During VIPS 3D printing (VIPS-3DP), a dissolved polymer-based ink is deposited in an environment where nebulized non-solvent is present, inducing the low-volatility solvent to be extracted from the filament in a controllable manner due to its higher chemical affinity with the non-solvent used. The polymeric phase is hardened in situ as a result of the induced phase separation process. The low volatility of the solvent enables its reclamation after the printing process, significantly reducing its environmental footprint. We first demonstrate the use of VIPS-3DP for polymer printing, showcasing its potential in printing intricate structures. We further extend VIPS-3DP to the deposition of polymer-based metallic inks or composite powder-laden polymeric inks, which become metallic parts or composites after a thermal cycle is applied. Furthermore, spatially tunable porous structures and functionally graded parts are printed by using the printing path to set the inter-filament porosity as well as an inorganic space-holder as an intra-filament porogen.

Concentration and reaction duration effects on synthesizing ZIF67 derivatives with NH4BF4 and NH4HF2 as efficient active material of energy storage device

Zeolitic imidazolate framework-67 (ZIF67) with large surface area and tunable pore structure is intensively applied as a tailoring target for design active materials. An in-situ tailoring technique is proposed to design ZIF67 derivatives by using structure directing agents (SDA) to induce favorable morphology and composition. Ammonium fluoride is a common SDA for modifying surface properties of active materials. With the same ammonium and similar fluorine-based groups, NH4BF4 and NH4HF2 are priming to play as SDA for synthesizing ZIF67 derivatives. In this study, the synthetic process of ZIF67 derivatives is tailored by varying the precursor concentration and reaction time in systems with NH4BF4 and NH4HF2 as SDA. The precursor concentration plays significant roles in the composition of ZIF67 derivatives. The reaction duration has higher influences on the morphology. The highest specific capacitance (CF) of 1347.0 F/g at 20 mV/s is achieved for the ZIF67 derivative synthesized using low concentration and 18 h, owing to favorable cobalt and nickel hydroxide compositions and two-dimensional sheet-like structure. An energy storage device composed of the optimal ZIF67 derivative and carbon electrodes shows a maximum energy density of 11.96 Wh/kg at 650 W/kg. The excellent cycling stability with CF retention of 83.6% and Coulombic efficiency of 92.0% is obtained after 10000 cycles.

3D Cellulose‐Based Solar Evaporator with Tunable Porous Structures for High Steam Generation

AbstractSolar vapor evaporation have emerged as a promising green technology to harvest fresh water. Achieving high evaporation rates while employing accessible and renewable materials is key focus in this field. Here, a 3D cylindrical‐shaped solar evaporator composed of natural cellulose is fabricated through ice‐templating freezing combined with crosslinking gelation. It demonstrates an evaporation rate of 4.2 kg m−2 h−1 under 1 sun irradiation, and reaches an energy efficiency of 173%, surpassing most reported cellulose/wood‐based evaporators. This enhanced performance is facilitated by absorbing energy from surrounding, possessing connected pores, and reducing the evaporation enthalpy. Moreover, a systematic exploration of the correlation between pore size and evaporation performance reveals that the reduced pore size (several micrometers) does not necessarily result in a higher evaporation rate, despite improving the fluid transportation. The interaction between water and cellulose induces the formation of intermediate water and reduces the evaporation enthalpy by more than 35%. Thus, the final evaporation performance is determined by a synergistic effect involving water transport, hydrophilicity, and vaporization enthalpy. Giving the high evaporation rate achieved, this 3D cellulose‐based solar evaporator presents a promising candidate toward a high‐throughput, eco‐friendly solar steam generation devices, aligning well with the criteria of green and sustainable development.

Nanoporous Silicon Materials Achieved by Electrochemical Method and Applications

Nanoporous materials have attracted extremely intense scientific attraction since the photoluminescence discovery at room temperature because of the quantum confinement effects. It is well known that in addition to the superior photoluminescence, nanoporous silicon materials prepared by the electrochemical method are promising materials for applications in catalysis, chemical, energy storage and biological sensing, due to its high porosity, modifiable surface, biocompatibility and biodegradability, which comprise with tunable optical porous Si structure and the applications such as biosensing, in vivo imaging, gas sensing and solar cells. Therefore, the facile electrochemical methods employed to synthesize the nanoporous materials are marked, especially for nanoporous silicon materials aim to provide the crucial information about the relevant techniques to consider the eco-friendly developments for the future environmental risks to diminish.

Transforming Mining Waste to Wealth: A Novel Process for the Sustainable Recovery and Utilization of Iron Tailings through HCl Leaching and MOFs Absorption

Rapid economic development and increased demand for mineral products in China have led to extensive extraction of various ores, resulting in significant environmental challenges associated with the generation of industrial solid waste, particularly iron tailings. Despite being a major mining nation, China faces issues of wasteful practices, with substantial amounts of valuable elements lost during the processing of iron ore. This study addresses the urgent need for sustainable solutions by proposing an innovative approach for the recovery of valuable elements from iron tailings. The proposed process involves a sequential application of acid leaching, chemical precipitation, and Metal-Organic Frameworks (MOFs) ion adsorption. The pre-treated iron tailings were leached in HCl solution with pH 1.5 at 70 °C for 2 h, and the co-leaching efficiency of 98.1% V, 98.2% Mo, 99.3% Fe, and 98.7% Mg was obtained. Chemical precipitation is then employed to isolate Fe, Mg V, and Mo and promote the formation of targeted compounds, ensuring concentration and purity. The integration of MOF ion adsorption, known for its high surface area and tunable pore structures, provides an efficient platform for selectively capturing and recovering target ions. 97.7% V and 96.3% Mo were selectively extracted from Zirconium 1,4-carboxybenzene metal-organic framework (UiO-66) adsorption system with pH 5.0 at 30 °C for 6 h, and 91.7% V and 90.3% Mo were selectively extracted from 2-methylimidazole zinc salt metal-organic framework (ZIF-8) adsorption system with pH 5 at 30 °C for 6.0 h. This three-stage process offers an efficient method for the recovery of valuable elements from iron tailings.