Adsorption of toluene with water on zeolitic imidazolate framework-8/graphene oxide hybrid nanocomposites in a humid atmosphere

Water vapor often present in the atmosphere will influence the adsorption of volatile organic compounds (VOCs). The competitive adsorption behavior of toluene and water vapor on synthesized zeolitic imidazolate framework-8 (ZIF-8) and graphene oxide (GO) hybrid composites was investigated in a humid atmosphere. The ZIF-8/GO composites were successfully prepared in a methanol system at room temperature and exhibited tunable nanoscale morphology and surface area, both determined by the GO content. A series of characterization techniques confirmed the formation of strong interactions between ZIF-8 and GO in the synthesized composites. Adsorption experiments demonstrated that the ZIF-8/GO composites with a GO content of 4 wt% had the highest toluene adsorption capacity of 116 mg g⁻¹ at a relative humidity (RH) of 55%, increased by 19% compared with pristine ZIF-8, and the recyclability of the adsorbent was investigated. The results showed that the synthesized ZIF-8/GO composites exhibited a higher toluene uptake capacity than pristine ZIF-8 crystals even at relatively high humidity, indicating that the ZIF-8/GO composites could be effective adsorbents in a humid atmosphere.

ZIF-8/GO composites can be used as efficient and recyclable adsorbents for the removal of toluene with water in a humid atmosphere.     

Functional activated carbon: from synthesis to groundwater fluoride removal

Developing green and functional adsorbents for the removal of inorganic pollutants from industrial wastewater is still a great challenge. Activated carbons (ACs) are promising eco-friendly materials for adsorption applications. This study reports on the preparation and functionalization of AC and its application for fluoride removal from water. Activated carbon was prepared from date stems, and the material was employed as a support for different modifications such as incorporation of Al(OH)₃, in situ dispersion of aluminum particles (Al⁰) and grafting of 3-(aminopropyl)triethoxysilane (APTES). The resulting functional adsorbents were fully characterized by Fourier transform infrared spectroscopy, scanning electronic microscopy, energy dispersive X-ray fluorescence, X-ray diffraction, differential scanning calorimetry and zeta potential analysis. The results evidenced successful surface modifications. All adsorbents had affinity for the removal of fluoride ions (F⁻). The highest F⁻ removal rate was up to 20 mg g⁻¹ for AC-Al(OH)₃. Removal of fluoride ions obeyed Langmuir isotherms and a second-order kinetic model, and reached 99% uptake. The AC-Al(OH)₃ adsorbent was successfully used to treat a groundwater solution contaminated by fluoride ions. These results open an interesting avenue for developing eco-friendly functionalized AC for adsorption applications.

Conversion and surface modification of date stems to obtain a relevant adsorbent to remove fluoride contamination.     

Glauconite clay-functionalized chitosan nanocomposites for efficient adsorptive removal of fluoride ions from polluted aqueous solutions

We herein have developed a mild approach for the fabrication of glauconite clay (G)-modified chitosan (CS) nanocomposites by the combination of a simple blending and crosslinking method. The chitosan was modified with ethylenediaminetetraacetic acid (EDTA), glutaraldehyde (GL), sodium dodecyl sulfate (SDS), and cetyltrimethyl ammonium bromide (CTAB). The as-prepared composites were identified using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), nitrogen physical adsorption (BET), atomic absorption spectrophotometry (AA), and thermal gravimetric analysis (TGA). The adsorption activities of the as-prepared materials were assessed for the removal of fluoride ions from aqueous media using a batch technique. Raw glauconite (G), GL-CS/G, SDS-CS/G, EDTA-GL-CS/G, and CTAB-CS/G adsorbents displayed maximum adsorption capacity values of 1.15, 4.31, 4.55, 6.90, and 9.03 mg g⁻¹, respectively. The adsorption results were well described by employing the pseudo-second-order kinetic and Langmuir isotherm models. The estimated thermodynamic constants indicated that the F⁻ ion adsorption was a spontaneous, physisorption process. Furthermore, the modified chitosan adsorbents are good candidates for the adsorptive elimination of F⁻ ions from aqueous solutions, according to their reusability, high stability, good adsorption capacity, and applicability for actual field water samples.

We herein have developed a mild approach for the fabrication of glauconite clay (G)-modified chitosan (CS) nanocomposites by the combination of a simple blending and crosslinking method.     

Carbon nanotubes/Al2O3 composite derived from catalytic reforming of the pyrolysis volatiles of the mixture of polyethylene and lignin for highly-efficient removal of Pb(ii)

In the present study, the coked catalysts derived from catalytic reforming of the pyrolysis volatiles of polyethylene (PE), lignin (LG) and their mixture were developed as low-cost and environmentally-friendly carbon materials-containing composites to remove heavy metal ions from aqueous solution. The composites were thoroughly characterized by SEM, TEM, XRD, TGA and FT-IR and then their adsorption capability towards Pb(ii) was investigated. It is found that curved cone-shape carbon nanotubes (CNTs) with abundant structural defects and O-containing surface functional groups, such as C–O, C O and –OH, can be obtained from the catalytic reforming of the mixture of PE and LG. The CNT-containing catalyst composite presents a superior adsorption capability towards Pb(ii) when it is employed in Pb(ii) removal. Adsorption isotherm and adsorption kinetics studies show that the adsorption process can be well simulated by the Langmuir isotherm and pseudo-second-order model, demonstrating that the adsorption is subjected to a homogeneous and chemical process. The calculated maximum adsorption capacity is as high as 146.08 mg g⁻¹, which is much higher than most of the adsorbents reported. Moreover, thermodynamic analysis reveals that the adsorption is spontaneous and endothermic. Accordingly, the used catalyst from the catalytic reforming can be developed as a low-cost and highly-efficient adsorbent.

The coked catalysts derived from catalytic reforming of the pyrolysis volatiles of polyethylene, lignin and their mixture were developed as low-cost and high-efficient carbon materials-containing composites to remove heavy metal ions from water.     

Facile preparation of porous organic copolymer based on triptycene and crown ether for efficient organic dye adsorption

There has been great interest in the use of porous polymers to remove organic dyes because of their adjustable surface area and task-specific functionality. We chose a triptycene-based porous polymer to ensure high porosity, and introduced crown ether into the sketch of the copolymer to significantly enhance the affinity for the organic dye molecules. Novel porous organic copolymers of triptycene and crown-ether-15 (POP-TCE-15) were obtained by a simple Friedel–Crafts reaction, and were highly effective in removing organic dyes from aqueous solution. POP-TCE-15 exhibited the best performance, with a maximum adsorption capacity of methylene blue, rhodamine B, and methyl orange of 787.4 mg g⁻¹, 421.9 mg g⁻¹, and 64.8 mg g⁻¹, respectively, which is better than most reported adsorbents. Their adsorption rates and adsorption isotherms were well fitted with pseudo-second-order kinetic models and the Langmuir model. More importantly, POP-TCE-15 can be effectively regenerated and recycled at least 5 times without any loss of adsorption capacity. With a hierarchical porous structure, high surface area, high hydrophobicity, and excellent adsorption capacity for dyes, the POP-TCE polymers could be ideal adsorbents for water purification and treatment.

The novel copolymer POP-TCE-15 displayed extraordinary capacity to adsorb organic dye from water.     

Regeneration performance of clay-based adsorbents for the removal of industrial dyes: a review

The present review covers the regeneration capacity and adsorption efficiency of different adsorbents for the treatment of industrial dyes to control water pollution. Various techniques and materials have been employed to remove organic pollutants from water; however, adsorption techniques using cost-effective, ecofriendly, clay-supported adsorbents are widely used owing to their simplicity and good efficiency. Among all the natural adsorbents, activated carbon has been found to be the most effective for dye adsorption; however, its use is restricted due to its high regeneration cost. Clays and modified clay-based adsorbents are the most efficient clarifying agents for organic pollutants as compared to activated carbon, organic/inorganic, and composite materials. Regeneration is an important aspect to stimulate the adsorption efficiency of the exhausted/spent adsorbent for water treatment. A number of techniques, including chemical treatment, supercritical extraction, thermal, and photocatalytic and biological degradation, have been developed to regenerate spent or dye-adsorbed clays. This review discusses how these techniques enhance the adsorption and retention potential of spent low-cost adsorbents and reflects on the future perspectives for their use in wastewater treatment.

The present review covers the regeneration capacity and adsorption efficiency of different adsorbents for the treatment of industrial dyes to control water pollution.     

Mesoporous TiO2–SiO2 adsorbent for ultra-deep desulfurization of organic-S at room temperature and atmospheric pressure

Ultra-deep desulfurization is a major requirement for upgrading the quality of fuel and power sources for fuel-cells. A series of mesoporous TiO₂–SiO₂ adsorbents were prepared and investigated for ultra-deep adsorption of benzothiophene (BT) and dibenzothiophene (DBT) from model fuel at ambient conditions. The adsorbents were characterized via SEM, XRD, N₂-BET, FT-IR and NH₃-TPD techniques. The results revealed that the adsorbent containing 40 wt% silica achieved the desulfurization efficiency higher than 99% when the initial sulfur concentration in the model fuel was 550 ppm. The high desulfurization performance of the adsorbent was attributed to its large specific surface and surface acidity. It also achieved a high sulfur adsorption capacity of 7.1 mg g⁻¹ in a fixed-bed test, while its static saturated sulfur capacity was 13.7 mg g⁻¹. The order of selectivity towards the adsorption of different organic sulfurs was DBT > BT&DBT > BT. The kinetics of the adsorption of organic sulfur was studied and the results indicated that the pseudo-second order model appropriately fitted the kinetics data. Furthermore, the used adsorbent can be easily regenerated and the desulphurization efficiency of the recovered adsorbent after five regeneration cycles was still maintained at 94.5%.

Ultra-deep desulfurization is a major requirement for upgrading the quality of fuel and power sources for fuel-cells.     

Recent developments in alginate-based adsorbents for removing phosphate ions from wastewater: a review

The huge development of the industrial sector has resulted in the release of large quantities of phosphate anions which adversely affect the environment, human health, and aquatic ecosystems. Naturally occurring biopolymers have attracted considerable attention as efficient adsorbents for phosphate anions due to their biocompatibility, biodegradability, environmentally-friendly nature, low-cost production, availability in nature, and ease of modification. Amongst them, alginate-based adsorbents are considered one of the most effective adsorbents for removing various types of pollutants from industrial wastewater. The presence of active COOH and OH⁻ groups along the alginate backbone facilitate its physical and chemical modifications and participate in various possible adsorption mechanisms of phosphate anions. Herein, we focus our attention on presenting a comprehensive overview of recent advances in phosphate removal by alginate-based adsorbents. Modification of alginate by various materials, including clays, magnetic materials, layered double hydroxides, carbon materials, and multivalent metals, is addressed. The adsorption potentials of these modified forms for removing phosphate anions, in addition to their adsorption mechanisms are clearly discussed. It is concluded that ion exchange, complexation, precipitation, Lewis acid–base interaction and electrostatic interaction are the most common adsorption mechanisms of phosphate removal by alginate-based adsorbents. Pseudo-2^nd order and Freundlich isotherms were figured out to be the major kinetic and isotherm models for the removal process of phosphate. The research findings revealed that some issues, including the high cost of production, leaching, and low efficiency of recyclability of alginate-based adsorbents still need to be resolved. Future trends that could inspire further studies to find the best solutions for removing phosphate anions from aquatic systems are also elaborated, such as the synthesis of magnetic-based alginate and various-shaped alginate nanocomposites that are capable of preventing the leaching of the active materials.

The huge development of the industrial sector has resulted in the release of large quantities of phosphate anions which adversely affect the environment, human health, and aquatic ecosystems.     

Ion-imprinted guanidine-functionalized zeolite molecular sieves enhance the adsorption selectivity and antibacterial properties for uranium extraction

The important properties in the development of adsorbents for uranium extraction from seawater include specific selectivity to uranium ions and anti-biofouling ability in the ocean environment. In this paper, we report a novel strategy for efficient selective extraction of uranium from aqueous solutions and good anti-bacterial properties by surface ion-imprinted zeolite molecular sieves. Guanidine-modified zeolite molecular sieves 13X (ZMS-G) were synthesized and used as the support for the preparation of uranium(vi) ion-imprinted adsorbents (IIZMS-G) by ligands with phosphonic groups. The prepared IIZMS-G adsorbent was characterized via Fourier transform infrared spectroscopy (FT-IR), scanning electronic microscopy (SEM), X-ray diffraction (XRD), and energy dispersive spectroscopy (EDS). The results showed that guanidine groups have been successfully introduced onto the support while its morphology structure was maintained. The adsorption performance and selectivity to U(vi) ions, antibacterial property, and reusability of IIZMS-G were evaluated. The results showed that the maximum adsorption capacity reached 141.09 mg g⁻¹ when the initial concentration of metal ions was 50 mg L⁻¹ at pH 6 and 20 °C. The adsorption process followed the pseudo-second-order kinetic model and Langmuir adsorption isotherm model. The IIZMS-G exhibits an efficient selective adsorption of U(vi) ions from aqueous solutions with competing ions. In addition, the IIZMS-G exhibited excellent inhibitory effects on Escherichia coli and Staphylococcus aureus, and the inhibitory rate was 99.99% and 98.96% respectively. These results suggest that the prepared IIZMS-G adsorbent may promote the development strategy of novel high selectivity and antifouling adsorbents for uranium recovery from seawater.

The important properties in the development of adsorbents for uranium extraction from seawater include specific selectivity to uranium ions and anti-biofouling ability in the ocean environment.     

Al-doped H2TiO3 ion sieve with enhanced Li+ adsorption performance

H₂TiO₃ (HTO) is considered to be one of the most promising adsorbents for lithium recovery from aqueous lithium resources duo to its highest theoretical adsorption capacity. However, its actual adsorption capacity is much lower owing to its unknown structure and incomplete leaching of lithium. After Al is doped into H₂TiO₃ (HTO-Al), the adsorption capacity of HTO-Al is 32.12 mg g⁻¹ and the dissolution of Ti is 2.53%. HTO-Al has good adsorption selectivity, and all the separation factors α are ≫1. Furthermore, HTO-Al also exhibits good cyclic stability and solubility resistance. After 5 cycles, the adsorption capacity remains 29.3 mg g⁻¹ and the dissolution rate is 1.7%. Therefore, HTO-Al has potential application value for recovering Li⁺ from aqueous lithium resources.

H₂TiO₃ (HTO) is considered to be one of the most promising adsorbents for lithium recovery from aqueous lithium resources duo to its highest theoretical adsorption capacity.     

Insight into the synergistic effect on adsorption for Cr(vi) by a polypyrrole-based composite

Polypyrrole-based (PPy) composite are promising candidates for the treatment of water pollution. Adsorption selectivity as well as a large adsorption capacity are two key factors for treating wastewater containing multiple ions. The structure and morphology of the prepared composites were characterized by the FT-IR, XRD and SEM examinations. The results indicate that the Fe₃O₄ and PPy nanosphere coats attapulgite (ATP) closely and evenly. Herein, a novel Fe₃O₄ and ATP doped three-dimensional network structure PPy/Fe₃O₄/ATP composite was demonstrated as an excellent adsorbent to effectively remove Cr(vi). The as-synthesized PPy/Fe₃O₄/ATP composite is suitable for Cr(vi) adsorption in a wide pH range (pH 2–6). Up to a 96.44% removal rate was found with 400 mg L⁻¹ Cr(vi) aqueous solution in 30 min for 0.2 g PPy/Fe₃O₄/ATP adsorbent. Adsorption results showed that Cr(vi) removal efficiency by PPy/Fe₃O₄/ATP decreased with an increase in pH. The removal rate of Cr(vi) had already reached 93.63% in 15 min contact time. Co-existing ions studies exhibit inorganic oxyacid anion and transition metal cation showed negative effects on Cr(vi) removal rate. A chemical rather than a physical adsorption occurred for these adsorbents as revealed by a pseudo-second-order kinetic study. The results of the adsorption isotherms showed that the adsorption process was similar to the Langmuir isotherm adsorption. Furthermore, the PPy/Fe₃O₄/ATP composite exhibited a high stability for Cr(vi) adsorption during recycling tests process. This work may provide some useful guidelines for designing adsorbents with selectivity toward specific heavy metal ions.

Polypyrrole-based (PPy) composite are promising candidates for the treatment of water pollution.     

Preparation of gemini surfactant/graphene oxide composites and their superior performance for Congo red adsorption

Gemini surfactant/GO composites (10-2-10/GO, 12-2-12/GO, and 14-2-14/GO) have been successfully prepared using three gemini surfactants with different tail chain lengths. The morphology and physicochemical properties of the as-synthesized composites were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform-infrared spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The gemini surfactant/GO composites were applied to the adsorption of Congo red dye, and from the experimental data, optimum adsorption conditions, adsorption kinetics, and isotherms were obtained. The removal process was favorable at acidic pH and reached equilibrium in ∼60 min. The results showed that the pseudo-second-order model and the Langmuir adsorption isotherm were a good fit for the adsorption of Congo red onto gemini surfactant/GO composites. Compared with other adsorbents reported in the literature, these composites showed superior Congo red adsorption capabilities, with absorption capacities as high as 2116, 2193, and 2325 mg g⁻¹ for 10-2-10/GO, 12-2-12/GO, and 14-2-14/GO, respectively. Moreover, the adsorption capacities were more than 1000 mg g⁻¹ even for the fifth cycle. The results of the present study substantiate that the gemini surfactant/GO composites are promising adsorbents for the removal of organic dyes in wastewater treatment.

Gemini surfactant/GO composites were prepared for the removal of Congo red dye, and show excellent adsorption capacities and reusabilities.     

Construction of a phosphate-rich polyacrylonitrile fiber surface microenvironment for efficient purification of crystal violet wastewater

Wastewater purification using fibrous adsorbents has received much attention due to their high efficiency, low cost, and recyclability. In this work, phosphate modified polyacrylonitrile fiber (B-PAN_EAPF) was prepared and used to remove cationic dyes. The B-PAN_EAPF showed the best adsorption capacity for crystal violet (CV) when compared with rhodamine B, methyl green, Victoria blue B, methylene blue, and neutral red. The adsorption tests revealed that the fiber possessed high adsorption efficiency and achieved semi-saturated adsorption within 15 min. The maximum adsorption capacity of 354.46 mg g⁻¹ as calculated by the Langmuir adsorption model was higher than many other adsorbents. Furthermore, the B-PAN_EAPF was used to remove 210 mL of CV in a continuous-flow process with a high removal efficiency over 90%. Besides, the phosphate functionalized fiber could easily decrease the concentration of CV to below 0.5 mg L⁻¹ which is below the maximum effluent discharge standard of 15 mg L⁻¹ prescribed in China. It could also be fully recovered and easily separated from the solution to achieve re-use 10 cycles. Moreover, the adsorption mechanism indicated that the adsorption process of the fiber for CV was mainly attributed to electrostatic interaction and hydrogen bonding. In conclusion, the results suggested that the B-PAN_EAPF characterized by its simplicity, efficiency, eco-friendliness, and reusability, could be a promising candidate for CV removal.

A novel recyclable phosphate functionalized polyacrylonitrile fiber shows excellent selectivity and adsorption capacity for crystal violet. It can be used to remove this dye in a flow process with high removal efficiency.     

Hydrogels derived from galactoglucomannan hemicellulose with inorganic contaminant removal properties

The adsorption of Cu(ii), Cd(ii), and Pb(ii) ions onto hydrogels derived from modified galactoglucomannan (GGM) hemicellulose was studied. GGM hemicellulose was modified with methacrylate groups (GGM-MA) to incorporate vinyl groups into the polymeric structure, which reacted later with synthetic monomers such as 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS). The results show that all the synthesized hydrogels were capable of adsorbing contaminating ions with high adsorption efficiency during short periods of time. Furthermore, an increase in the content of GGM-MA generated a hydrogel (H3) with a similar ion adsorption property to the other hydrogels but with a lesser degree of swelling. The H3 hydrogel had an adsorption capacity of 60.0 mg g⁻¹ Cd(ii), 78.9 mg g⁻¹ Cu(ii), and 174.9 mg g⁻¹ Pb(ii) at 25 °C. This result shows that modified GGM hemicelluloses can be employed as renewable adsorbents to remove Cu(ii), Cd(ii), and Pb(ii) ions from aqueous solutions.

The adsorption of Cu(ii), Cd(ii), and Pb(ii) ions onto hydrogels derived from modified galactoglucomannan (GGM) hemicellulose was studied.     

Batch and fixed-bed column studies for selective removal of cesium ions by compressible Prussian blue/polyurethane sponge

In this work, compressible Prussian blue/polyurethane sponges (PB@PUS) for selective removal of cesium ions were prepared via an in situ radiation chemical route. The characterization results indicate that uniform PB nanoparticles were successfully synthesized and well dispersed on the porous skeleton of sponge. Batch and fixed-bed column experiments were detailedly conducted to investigate their adsorption performances. Batch adsorption experiments reveal that PB@PUS exhibited good selective removal property for cesium ions in a wide range of pH, whose maximal adsorption capacity and removal efficiency reached 68.6 mg g⁻¹ and 99%, respectively. The adsorption processes could be described by the Langmuir isotherm adsorption model and pseudo-second-order adsorption kinetic model. The fixed-bed column experiments show that the breakthrough and exhaustion time obviously increased with the decrease of flow rate and initial cesium ions concentration. The breakthrough curves could be well fitted by the Thomas model and Yoon–Nelson model. The theoretical saturated adsorption capacity of PB@PUS-3 calculated from the Thomas model was 68.2 mg g⁻¹. The as-prepared samples were light, stable and compressible, which can be applied in radioactive wastewater treatment.

Compressible Prussian blue/polyurethane sponges for selective removal of cesium ions were prepared and detailedly studied via fixed-bed column/batch adsorption experiments.     

A green l-cysteine modified cellulose nanocrystals biosorbent for adsorption of mercury ions from aqueous solutions

Using a green biosorbent to remove toxic mercury ions from aqueous solutions is a significant undertaking. In the present study, a novel biosorbent, l-cysteine modified cellulose nanocrystals (Lcys-CNCs), was prepared by functionalizing high surface area cellulose nanocrystals with l-cysteine through periodate oxidation and reductive amination reaction. Lcys-CNCs were characterized by FT-IR, ¹³C CP-MAS NMR, elemental analysis, XPS, zeta potential and SEM. As cellulose nanocrystals are the natural nanomaterial, and l-cysteine contains strong mercury chelating groups, Lcys-CNCs show excellent adsorption capacity for mercury ions. The experimental conditions such as pH, contact time, and initial mercury ion concentration are discussed. The pseudo-second order model can describe the removal kinetics of Hg(ii) more accurately than the pseudo-first order model. The adsorption isotherm study of Hg(ii) followed the Langmuir model of monolayer adsorption. The maximum uptake capacity of Lcys-CNCs was determined to be 923 mg g⁻¹. Lcys-CNCs can remove mercury ions with 93% removal efficiency within 5 min from a 71 mg L⁻¹ solution. For Cd(ii), Pb(ii), Cu(ii) and Zn(ii) ions, Lcsy-CNCs can selectively adsorb Hg(ii) ions and the removal efficiency is 87.4% for Hg(ii). This study suggests Lcsy-CNCs are a green and highly efficient biosorbent for adsorption of mercury ions from aqueous solutions.

A green biosorbent, l-cysteine modified cellulose nanocrystals, was successfully synthesized and applied to adsorb mercury ions from aqueous solutions.     

Optimum selective separation of Cu(ii) using 3D ordered macroporous chitosan films with different pore sizes

Although bio-materials are widely used for the adsorption of heavy metal ions, they have low specific surface area, slow adsorption rates, and poor selectivity. To overcome these limitations, in this study, we report a 3D-ordered macroporous ion-imprinted chitosan film (3DOM-IICF); the 3DOM-IICF coupled with a colloidal crystal template and ion imprinting (IIP) technology has been used to absorb copper ions (Cu(ii)) present in water. Moreover, polystyrene (PS) micro-spheres and copper templates were added to form a three-dimensional ordered macroporous structure and ion-imprinted sites, respectively. Finally, the film was formed by drying. Adsorption experiments showed the removal of Cu(ii) from the 3DOM-IICF in an aqueous solution. The 3DOM-IICF exhibited good adsorption performance under neutral conditions of pH = 7.0, and the adsorption efficiency was high. The maximum adsorption capacity of the 3DOM-IICF was 261.31 mg g⁻¹. The adsorption processes were more consistent with the pseudo-second-order kinetic model and the Langmuir isotherm. The 3DOM-IICF exhibits superior selective adsorption of Cu(ii). Moreover, the 3DOM-IICF could be regenerated multiple times, reused as an adsorbent and maintained high adsorption capacity. This kind of imprinted template method has important significance in the selective adsorption of pollutants in bio-materials and is worthy of in-depth research.

3DOM-IICF coupled with colloidal crystal template and ion imprinting technology (IIP) was used to absorb copper ions (Cu(ii)) in water. Added polystyrene (PS) micro-spheres to form a three-dimensional ordered macroporous structure.     

Chitosan-derived three-dimensional porous carbon for fast removal of methylene blue from wastewater

Despite much progress in modifying chitosan as an absorbent for wastewater treatment, it is still difficult for current chitosan-based adsorbents to achieve the desired removal effects towards basic dyes. In this study, chitosan-derived three-dimensional porous carbon (CTC) consisting of large-diameter channels and mesopores was prepared to remove methylene blue (MB) from wastewater. The results indicate that CTC has excellent performance for MB removal, and the maximum adsorption capacity was 925.93 mg g⁻¹ at 318 K. The adsorption isotherm and kinetics models of MB on CTC could be described well by the Langmuir isotherms and the pseudo-second-order rate model. An experiment to study the CTC removal of MB from a flowing aqueous solution was performed using a homemade device. The water treatment rate of CTC reached 250 L g⁻¹ h⁻¹, with high MB removal efficiency (>93.4%). Furthermore, the desorption–adsorption experiments indicate that CTC is also a reusable adsorbent that can be applied to recover MB from wastewater. The obtained CTC is a promising alternative for the current expensive absorbents and provides a concept for designing the three-dimensional (3D) structures of raw materials to improve adsorption capability.

The chitosan-derived three-dimensional porous carbon (CTC) consisting of large-diameter channels and mesopores was prepared by two steps activation and used for the removal of methylene blue (MB) from wastewater.     

Metal–organic frameworks (MOFs) based nanofiber architectures for the removal of heavy metal ions

Environmental heavy metal ions (HMIs) accumulate in living organisms and cause various diseases. Metal–organic frameworks (MOFs) have proven to be promising and effective materials for removing heavy metal ions from contaminated water because of their high porosity, remarkable physical and chemical properties, and high specific surface area. MOFs are self-assembling metal ions or clusters with organic linkers. Metals are used as dowel pins to build two-dimensional or three-dimensional frameworks, and organic linkers serve as carriers. Modern research has mainly focused on designing MOFs-based materials with improved adsorption and separation properties. In this review, for the first time, an in-depth look at the use of MOFs nanofiber materials for HMIs removal applications is provided. This review will focus on the synthesis, properties, and recent advances and provide an understanding of the opportunities and challenges that will arise in the synthesis of future MOFs–nanofiber composites in this area. MOFs decorated on nanofibers possess rapid adsorption kinetics, a high adsorption capacity, excellent selectivity, and good reusability. In addition, the substantial adsorption capacities are mainly due to interactions between the target ions and functional binding groups on the MOFs–nanofiber composites and the highly ordered porous structure.

Metal–organic frameworks (MOFs) are promising and effective materials for removing heavy metal ions from contaminated water owing to their high porosity, remarkable physical and chemical properties, and high specific surface area.     

Removal of Hg(ii) in aqueous solutions through physical and chemical adsorption principles

Adsorption has been the focus of research on the treatment of heavy metal mercury pollution since it is among the most toxic heavy metals in existence. The US EPA has set a mandatory discharge limit of 10 μg Hg L⁻¹ for wastewater and for drinking water a maximum accepted concentration of 1 μg Hg L⁻¹. Physical adsorption and chemical adsorption are the two major mechanisms of adsorption methods used for mercury removal in aqueous sources. The recent decades'' research progress is reviewed to elaborate varieties of adsorption materials ranging from materials with large surface area for physical adsorption to metal oxides for chemical adsorption. Many examples are presented to illustrate the adsorption principles and clarify the relationship between the structure and performance of the adsorbents. The combination of physical adsorption and chemical adsorption gives rise to numbers of potential mercury removal composites. This review demonstrates the adsorption mechanism and the performance of varieties of adsorbents, which would provide a comprehensive understanding on the design and fabrication of new materials for the removal of heavy metal ions in water.

Adsorption has been the focus of research on the treatment of heavy metal mercury pollution since it is among the most toxic heavy metals in existence.