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Orderly Porous Covalent Organic Frameworks-based Materials: Superior Adsorbents for Pollutants Removal from Aqueous Solutions.

ABSTRACT: Covalent organic frameworks (COFs) are a new type of crystalline porous polymers known for chemical stability, excellent structural regularity, robust framework, and inherent porosity, making them promising materials for capturing various types of pollutants from aqueous solutions. This review thoroughly presents the recent progress and advances of COFs and COF-based materials as superior adsorbents for the efficient removal of toxic heavy metal ions, radionuclides, and organic pollutants. Information about the interaction mechanisms between various pollutants and COF-based materials are summarized from the macroscopic and microscopic standpoints, including batch experiments, theoretical calculations, and advanced spectroscopy analysis. The adsorption properties of various COF-based materials are assessed and compared with other widely used adsorbents. Several commonly used strategies to enhance COF-based materials' adsorption performance and the relationship between structural property and sorption ability are also discussed. Finally, a summary and perspective on the opportunities and challenges of COFs and COF-based materials are proposed to provide some inspiring information on designing and fabricating COFs and COF-based materials for environmental pollution management.

SUBMITTER: Liu X

PROVIDER: S-EPMC8454561 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Crystalline Covalent Organic Frameworks from Triazine Nodes as Porous Adsorbents for Dye Pollutants.

Project description:The development of covalent organic frameworks (COFs) with nodes and spacers, designed to maximize their functional properties, is a challenge. Triazines exhibit better electron affinity than benzene-based aromatic rings; therefore, structures based on 1,3,5-substituted triazine-centered nodes are more stable than those from 1,3,5-benzene-linked COFs. Compared to COFs prepared from flat, rigid sp2 carbon-linked triazine nodes, the O-linked flexible tripodal triazine-based COF demonstrates several unpredictable properties such as an increase in crystallinity and cavity size. In this study, the COF prepared from O-linked flexible 2,4,6-tris(p-formylphenoxy)-1,3,5-triazine serves as an excellent absorbent for removing methylene blue from water. Our results demonstrate that COF is highly stable in water and functions as a robust adsorbent. Its adsorption isotherm is consistent with the Langmuir model and its adsorption kinetics follows a pseudo-second order model. Moreover, the COF was characterized using elemental analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, solid-state ultraviolet-visible spectroscopy, and X-ray diffraction. It exhibited permanent porosity, a high specific surface area (279.5 m2·g-1), and was chemically and thermally stable. Photophysical studies revealed that the COF exhibits a low bandgap energy value of 3.07 eV, indicating its semiconducting nature.

| S-EPMC6941375 | biostudies-literature

Rapid Room-Temperature Preparation of Hierarchically Porous Metal-Organic Frameworks for Efficient Uranium Removal from Aqueous Solutions.

Project description:The effective removal of uranium from an aqueous solution is a highly valuable process for the environment and health. In this study, we developed a facile and rapid method to synthesize hierarchically porous Cu-BTC (RT-Cu-BTC) using a cooperative template strategy. The as-synthesized RT-Cu-BTC exhibited hierarchically porous structure and excellent thermostability, as revealed by X-ray powder diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. Compared with conventional metal-organic frameworks (MOFs) and zeolites, the obtained RT-Cu-BTC exhibited enhanced adsorption capacity (839.7 mg·g-1) and high removal efficiency (99.8%) in the capture of uranium (VI) from aqueous solutions. Furthermore, the conditions such as adsorbent dose, contact time, and temperature in adsorption of uranium (VI) by RT-Cu-BTC were investigated in detail. The thermodynamics data demonstrated the spontaneous and endothermic nature of the uranium (VI) adsorption process. The Langmuir isotherm and pseudo-second-order models could better reflect the adsorption process of uranium (VI) onto RT-Cu-BTC. In addition, the as-synthesized RT-Cu-BTC showed excellent stability in removing uranium (VI) from an aqueous solution. This work provides a facile and rapid approach for fabricating hierarchically porous MOFs to realize a highly efficient removal of uranium (VI) from aqueous systems.

| S-EPMC7466529 | biostudies-literature

Ambient aqueous-phase synthesis of covalent organic frameworks for degradation of organic pollutants.

Project description:The development of a mild, low cost and green synthetic route for covalent organic frameworks (COFs) is highly desirable in order to open the door for practical uses of this new family of crystalline porous solids. Herein, we report a general and facile strategy to prepare a series of microporous or mesoporous COFs by a β-ketoenamine based Michael addition-elimination reaction in aqueous systems at ambient temperature and pressure. This synthesis method not only produces highly crystalline and porous COFs, but also can be carried out with a high reaction rate (only 30 min), high yields (as high as 93%) and large-scale preparation (up to 5.0 g). Furthermore, an Fe(ii)-doped COF shows impressive performance in the oxidative degradation of organic pollutants in aqueous medium. This research thus provides a promising pathway to large-scale green preparation of COFs and their potential application in environmental remediation.

| S-EPMC7066675 | biostudies-literature

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| S-EPMC8623111 | biostudies-literature

Arsenic removal from aqueous solutions using Fe3O4-HBC composite: effect of calcination on adsorbents performance.

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| S-EPMC4072660 | biostudies-literature

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| S-EPMC9056622 | biostudies-literature

Zirconium Component Modified Porous Nanowood for Efficient Removal of Phosphate from Aqueous Solutions.

Project description:Rapid urban industrialization and agricultural production have led to the discharge of excessive phosphate into aquatic systems, resulting in a rise in water pollution. Therefore, there is an urgent need to explore efficient phosphate removal technologies. Herein, a novel phosphate capture nanocomposite (PEI-PW@Zr) with mild preparation conditions, environmental friendliness, recyclability, and high efficiency has been developed by modifying aminated nanowood with a zirconium (Zr) component. The Zr component imparts the ability to capture phosphate to the PEI-PW@Zr, while the porous structure provides a mass transfer channel, resulting in excellent adsorption efficiency. Additionally, the nanocomposite maintains more than 80% phosphate adsorption efficiency even after ten adsorption-desorption cycles, indicating its recyclability and potential for repeated use. This compressible nanocomposite provides novel insights into the design of efficient phosphate removal cleaners and offers potential approaches for the functionalization of biomass-based composites.

| S-EPMC10254632 | biostudies-literature

An Innovative Porous Nanocomposite Material for the Removal of Phenolic Compounds from Aqueous Solutions.

Project description:Energy efficient, low-cost, user-friendly, and green methods for the removal of toxic phenolic compounds from aqueous solution are necessary for waste treatment in industrial applications. Herein we present an interesting approach for the utilization of oxidized carbon nanotubes (CNTs) in the removal of phenolic compounds from aqueous solution. Dried pristine CNTs were stably incorporated in a solid porous support of polydimethylsiloxane (PDMS) facilitating the handling during both oxidation process of the nanomaterial and uptake of phenolic compounds, and enabling their safe disposal, avoiding expensive post-treatment processes. The adsorption studies indicated that the materials can efficiently remove phenolic compounds from water with different affinities towards different phenolic compounds. Furthermore, the adsorption kinetics and isotherms were studied in detail. The experimental data of adsorption fitted well with Langmuir and Freundlich isotherms, and pseudo-second-order kinetics, and the results indicated that the adsorption process was controlled by a two-step intraparticle diffusion model. The incorporation of CNTs in polymeric matrices did not affect their functionality in phenol uptake. The material was also successfully used for the removal of phenolic compounds from agricultural waste, suggesting its possible application in the treatment of wastewater. Moreover, the surface of the material could be regenerated, decreasing treatment costs.

| S-EPMC5977348 | biostudies-literature

Investigation of Cross-Linked Chitosan-Based Membranes as Potential Adsorbents for the Removal of Cu2+ Ions from Aqueous Solutions

Project description:Rapid industrialization has led to huge amounts of organic pollutants and toxic heavy metals into aquatic environment. Among the different strategies explored, adsorption remains until the most convenient process for water remediation. In the present work, novel cross-linked chitosan-based membranes were elaborated as potential adsorbents of Cu2+ ions, using as cross-linking agent a random water-soluble copolymer P(DMAM-co-GMA) of glycidyl methacrylate (GMA) and N,N-dimethylacrylamide (DMAM). Cross-linked polymeric membranes were prepared through casting aqueous solutions of mixtures of P(DMAM-co-GMA) and chitosan hydrochloride, followed by thermal treatment at 120 °C. After deprotonation, the membranes were further explored as potential adsorbents of Cu2+ ions from aqueous CuSO4 solution. The successful complexation of copper ions with unprotonated chitosan was verified visually through the color change of the membranes and quantified through UV-vis spectroscopy. Cross-linked membranes based on unprotonated chitosan adsorb Cu2+ ions efficiently and decrease the concentration of Cu2+ ions in water to a few ppm. In addition, they can act as simple visual sensors for the detection of Cu2+ ions at low concentrations (~0.2 mM). The adsorption kinetics were well-described by a pseudo-second order and intraparticle diffusion model, while the adsorption isotherms followed the Langmuir model, revealing maximum adsorption capacities in the range of 66–130 mg/g. Finally, it was shown that the membranes can be effectively regenerated using aqueous H2SO4 solution and reused.

| S-EPMC10004399 | biostudies-literature

Optimal Synthesis of Novel Phosphonic Acid Modified Diatomite Adsorbents for Effective Removal of Uranium(VI) Ions from Aqueous Solutions.

Project description:The authors synthesized a series of functionalized diatomite-based materials and assessed their U(VI) removal performance. Phosphor-derivative-modified diatomite adsorbents were synthesized by the three-route procedures: polymerisation (DIT-Vin-PAin), covalent (DIT-Vin-PAcov), and non-covalent (DIT-PA) immobilization of the functional groups. The effects of the diatomite modification have been studied using powder XRD, solid state NMR, FTIR spectroscopy, electronic microscopy, EDX, acid-base titrations, etc. The maximum adsorption capacities of DIT-Vin-PAcov, DIT-PA, and DIT-Vin-PAin samples were 294.3 mg/g, 253.8 mg/g, and 315.9 mg/g, respectively, at pH0 = 9.0. The adsorption amount of U(VI) ions using the prepared DIT-Vin-PAin was 95.63%, which is higher compared with that of the natural diatomite at the same concentration. The adsorption studies demonstrated that the phosphonic and hydroxyl groups on the surface of the diatomite played pivotal roles in the U(VI) adsorption. The U(VI) ions as a "hard" Lewis acid could easily form bonds with the "hard" donor P-containing ligands, so that the as-prepared DIT-Vin-PAin sample had excellent adsorption properties. The monolayer adsorption of the analyte on the surface of the raw diatomite and DIT-PA was observed. It was found from the thermodynamic parameters that the uptake of the U(VI) ions by the obtained adsorbents was a spontaneous process with an endothermic effect. Findings of the present work highlight the potential for using modified diatomite as effective and reusable adsorbents for the extraction of U(VI) in the waste, river, and tap waters with satisfactory results.

| S-EPMC10419580 | biostudies-literature

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