High Adsorption Efficiency Research Articles

Phospholipid Bilayer Inspired Sandwich Structural Nanofibrous Membrane for Atmospheric Water Harvesting and Selective Release.

Atmospheric water harvesting (AWH) has been broadly exploited to meet the challenge of water shortage. Despite the significant achievements of AWH, the leakage of hydroscopic salt during the AWH process hinders its practical applications. Herein, inspired by the unique selective permeability of the phospholipid bilayer, a sandwich structural (hydrophobic-hydrophilic-hydrophobic) polyacrylonitrile nanofibrous membrane (San-PAN) was fabricated for AWH. The hydrophilic inner layer loaded with LiCl could capture water from the air. The hydrophobic microchannels in the outer layer could selectively allow the free transmission of gaseous water molecules but confine the hydroscopic salt solution in the hydrophilic layer, achieving continuous and recyclable water sorption/desorption. As demonstrated, the as-prepared AWH devices presented high-efficient adsorption kinetics from 1.66 to 4.08 g g-1 at 30% to 90% relative humidity. Thus, this work strengthens the understanding of the water transmission process along microchannels and provides insight into the practical applications of AWH.

Analysis of the Efficiency of Landfill Gas Treatment for Power Generation in a Cogeneration System in Terms of the European Green Deal

Climate change and environmental degradation pose a threat to Europe and the world. The mechanism that will address these challenges is the European Green Deal, which envisions transforming the EU into a modern, resourceful, economical and competitive economy, aiming for zero greenhouse gas emissions. Landfill gas generated in a landfill waste deposit poses a threat to the environment and people. In this aspect, its capture, treatment and safe neutralization or use for energy purposes are important. Treatment of landfill gas, which is the fuel for gas engines in cogeneration units, is crucial for their proper operation and the quantity and quality of electricity and heat generated. The purpose of this study was to perform research to determine the hydrogen sulfide content of landfill gas and the actual efficiency of hydrogen sulfide removal from the gas using activated carbon. The tests performed constitute the basis for the reliable operation of gas engines in cogeneration installations and are dedicated mainly to the operators of these installations. Accordingly, three measurement campaigns were carried out, each with 42 measurements, the first for the “raw” gas obtained directly from the landfill, the second for the gas before entering the carbon filter and the third after its treatment. In addition, surface analysis was performed, and the elemental composition of the “fresh” molded activated carbon constituting the filter material was determined using a scanning electron microscope with an EDS system. The results showed a high elemental content of carbon in the test sample at 92.78%, while the efficiency of hydrogen sulfide removal from landfill gas by activated carbon, calculated from the measurements, was 97.05%. The obtained test results confirmed the validity of using impregnated activated carbon to remove hydrogen sulfide from landfill gas and its high adsorption efficiency, which can consequently result in reliable operation of the gas engine in the cogeneration unit and ultimately fit in with the objectives of the European Green Deal. The research results are an incentive for operators of cogeneration installations to systematically examine the quality of landfill gas and the efficiency of biogas purification devices.

High efficiency adsorption of uranium by magnesia-silica-fluoride co-doped hydroxyapatite

Hydroxyapatite has a high affinity to uranium, and element doping can effectively improve its adsorption performance. In this study, magnesia-silica-fluoride co-doped hydroxyapatite composite was prepared by hydrothermal method, and the effect of single-phase and multiphase doping on the structure and properties of the composites was investigated. The results showed that the specific surface area of Mg–Si–F-nHA composites increased by 63.01% after doping. Comparing with nHA, U(VI) adsorption capacity of Si-nHA, Mg–Si-nHA and Mg–Si–F-nHA composites increased by 13.01%, 17.39% and 22.03%, respectively. The adsorption capacity of Mg–Si–F-nHA composite reached 1286.76 mg/g. Adsorbent dosage and pH obviously affected U(VI) adsorption, and the experimental data can be fitted well by PSO and Sips models. The physicochemical characterization before and after adsorption suggested that complexation, ion exchange and precipitation participated in uranium adsorption. In conclusion, different elements doping can effectively improve the uranium adsorption properties of hydroxyapatite composites.

Removal of lead ions (Pb2+) from aqueous solution using chitosan/starch composite material: Experimental and density functional theory findings

AbstractTreatment of wastewater has become vital to prevent environmental pollution in recent years. Adsorption is an easily applicable, low-cost and efficient method and is the subject of this study. In this study, an adsorbent was synthesized to be used in heavy metal removal using chitosan and starch. The composite was characterized by Fourier transform infrared (FTIR) spectrophotometry, X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) analysis. It was determined that the composite had an amorphous and compact structure. Adsorption experiments were carried out under the optimized parameters such as solution pH, concentration, adsorbent amount, equilibrium time, and temperature. It shows that during adsorption, with the increase in pH, the adsorption efficiency and adsorption capacity first increase and then a fluctuation occurs. The highest adsorption efficiency and Q value were reached at pH 3.46 as 78% and 0.038 mol/kg, respectively. Moreover, the adsorption capacity (Q) reached its highest value with a value of 0.067 mol/kg in the presence of 30 mg adsorbent. Equilibrium experiments were validated by the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. To investigate the adsorption mechanism, pseudo-first-order (PFO) and pseudo-second-order (PSO) kinetic models were used. It was determined that the adsorption process followed the D-R isotherm (R2 = 0.99) and PSO (R2 = 0.99). Therefore, the existence of chemical adsorption can be mentioned. Thermodynamic parameters enthalpy (∆H), Gibbs free energy (∆G) and entropy change (∆S) were investigated. The adsorbate-adsorbent interactions were studied by density functional theory (DFT).

Manganese dioxide decorated kiwi peel powder for efficient removal of lead from aqueous solutions, blood and Traditional Chinese Medicine extracts

For human health and environment safety, it is of great significance to develop novel materials with high effectiveness for removal of lead from not only aqueous solutions but also human body and traditional Chinese medicines. Here, functional kiwi peel composite, manganese dioxide decorated kiwi peel powder (MKPP), is proposed for the removal of Pb2+ effectively. The adsorption of Pb2+ in aqueous solution is a highly selective and endothermic process and kinetically follows a pseudo-second-order model, which can reach equilibrium with the capacity of 192.7 mg/g within 10 min. Comprehensive factors of hydration energy, charge-to-radius ratio and softness of Pb2+ make a stronger affinity between MKPP and Pb2+. The possible adsorption mechanism involves covalent bond, electrostatic force and chelation, etc. MKPP can be efficiently regenerated and reused with high adsorption efficiency after five cycles. Besides, MKPP can remove over 97% of Pb2+ from real water samples. MKPP can also alleviate lead poisoning to a certain extent and make the Pb level of TCM extract meet the safety standard. This work highlights that MKPP is a promising adsorbent for the removal of Pb2+ and provides an efficient strategy for reusing kiwi peel as well as dealing with the problem of Pb pollution.

Nano‑selenium functionalized chitosan gel beads for Hg(II) removal from apple juice

The presence of potentially toxic elements and compounds poses threats to the quality and safety of fruit juices. Among these, Hg(II) is considered as one of the most poisonous heavy metals to human health. Traditional chitosan-based and selenide-based adsorbents face challenges such as poor adsorption capacity and inconvenient separation in juice applications. In this study, we prepared nano‑selenium functionalized chitosan gel beads (nanoSe@CBs) and illustrated the synergistic promotions between chitosan and nanoSe in removing Hg(II) from apple juice. The preparation conditions, adsorption behaviors, and adsorption mechanism of nanoSe@CBs were systematically investigated. The results revealed that the adsorption process was primarily controlled by chemical adsorption. At the 0.1 % dosage, the adsorbent exhibited high uptake, and the maximum adsorption capacity from the Langmuir isotherm model could reach 376.5 mg/g at room temperature. The adsorbent maintained high adsorption efficiency (> 90 %) across a wide range of Hg(II) concentrations (0.01 to 10 mg/L) and was unaffected by organic acids present in apple juice. Additionally, nanoSe@CBs showed negligible effects on the quality of apple juice. Overall, nanoSe@CBs open up possibilities to be used as a safe, low-cost and highly-efficient adsorbent for the removal of Hg(II) from juices and other liquid foods.

Construction of defective hydroxyl-rich metal–organic framework for effective capture of borate ion

Developing high-efficiency adsorbents for borate ion still remains up to now. Herein, a facile and green method is used to obtain serial hydroxyl functionalized UiO-66-(OH)2-AA-X (AA, acetic acid; X, AA usage) by using AA as a modulator. The addition of AA can induce the generation of defect units in the adsorbents due to its partial substitution for the organic linkers. It is found that the defect degree as well as the porosity can be neatly regulated by the AA amount. In particular, UiO-66-(OH)2-AA-20 with the most defects exhibits a high adsorption capacity (891.1 mg g−1) towards borate ion, outperforming the most previously reported adsorbents. The adsorption reaches equilibrium at 600 min. The adsorption behavior can be well described by the Langmuir isotherm model and pseudo-second-order model. Besides, UiO-66-(OH)2-AA-20 possesses a wide pH (3–10) tolerance, excellent anti-interference ability, and good reusability. A combination of experimental characterization and density functional theory calculation indicates the free hydroxyl groups serve as the main adsorption sites, and the adsorption-driven forces involve electrostatic, coordination, hydrogen bonds and π–π stacking interactions. On these basis, our work may provide a guideline for constructing high-efficiency defective adsorbents for borate ions via a modulated strategy.

Immobilization of ionic liquids onto chloromethylated polystyrene as a strategy for highly efficient and selective recovery of Au(III) from gold slag and PCBs

The recovery of Au(III) has become a focal point of interest due to its significance in resource utilization and addressing environmental contamination. In this study, [C3NH2Mim]Cl-CMPS and PPh3-CMPS were successfully developed by immobilizing [C3NH2Mim]Cl and triphenylphosphine (PPh3) onto chloromethylated polystyrene beads (CMPS). The adsorbents demonstrated consistently high adsorption efficiency (>95 %) at a wide pH range. The [C3NH2Mim]Cl-CMPS and PPh3-CMPS exhibited exceptional selective adsorption ability for Au(III), and the adsorption process adhered to the PSO and Langmuir model. The adsorption efficiency of Au(III) remained constant after five consecutive cycles, highlighting outstanding reusability performance. Furthermore, as the existence of multiple coexisting metal ions, [C3NH2Mim]Cl-CMPS and PPh3-CMPS could efficiently and selectively capture Au(III) from the gold slag and PCBs lixivium, which is promising for Au recovery in practice.

A Magnetic Reduced Graphene Oxide Nanocomposite: Synthesis, Characterization, and Application for High-Efficiency Detoxification of Aflatoxin B1.

(1) Background: Safety problems associated with aflatoxin B1 (AFB1) contamination have always been a major threat to human health. Removing AFB1 through adsorption is considered an attractive remediation technique. (2) Methods: To produce an adsorbent with a high AFB1 adsorption efficiency, a magnetic reduced graphene oxide composite (Fe3O4@rGO) was synthesized using one-step hydrothermal fabrication. Then, the adsorbent was characterized using a series of techniques, such as SEM, TEM, XRD, FT-IR, VSM, and nitrogen adsorption-desorption analysis. Finally, the effects of this nanocomposite on the nutritional components of treated foods, such as vegetable oil and peanut milk, were also examined. (3) Results: The optimal synthesis conditions for Fe3O4@rGO were determined to be 200 °C for 6 h. The synthesis temperature significantly affected the adsorption properties of the prepared material due to its effect on the layered structure of graphene and the loading of Fe3O4 nanoparticles. The results of various characterizations illustrated that the surface of Fe3O4@rGO had a two-dimensional layered nanostructure with many folds and that Fe3O4 nanoparticles were distributed uniformly on the surface of the composite material. Moreover, the results of isotherm, kinetic, and thermodynamic analyses indicated that the adsorption of AFB1 by Fe3O4@rGO conformed to the Langmuir model, with a maximum adsorption capacity of 82.64 mg·g-1; the rapid and efficient adsorption of AFB1 occurred mainly through chemical adsorption via a spontaneous endothermic process. When applied to treat vegetable oil and peanut milk, the prepared material minimized the loss of nutrients and thus preserved food quality. (4) Conclusions: The above findings reveal a promising adsorbent, Fe3O4@rGO, with favorable properties for AFB1 adsorption and potential for food safety applications.

γ-AlOOH decorated 3D-reduce graphene oxide: An effective adsorbent for removal of methylene blue and ciprofloxacin

Engineering and synthesis of high-efficiency adsorbent is imperative for water purification. Herein, γ-AlOOH nanoflakes were in-situ decorated onto 3D-reduced graphene oxide (3D-rGO) with the intention of augmenting the specific surface area and ameliorating the adsorption capacity of 3D-rGO in virtue of a facile one-step hydrothermal method. The detailed morphological and structural information of γ-AlOOH/3D-rGO nanocomposite were captured via various instruments. γ-AlOOH/3D-rGO exhibited outstanding removal efficiency towards methylene blue (MB) and ciprofloxacin (CIP) due to its abundant mesopores, increased specific surface area and 3D macro structure. The MB model could well describe the MB adsorption behavior and CIP adsorption process can be fitted by the Elovich model. Isotherm fitting results proclaim that MB adsorption and CIP adsorption followed the Langmuir model; and γ-AlOOH/3D-rGO possessed outstanding adsorption for MB and CIP with the maximum adsorption capacity of 930.0889 mg/g at 288 K and 353.9148 mg/g at 318 K, respectively. The MB and CIP adsorption onto γ-AlOOH/3D-rGO should be the results of the joint action of hydrogen bonds, π-π interaction and complexation. γ-AlOOH/3D-rGO also exhibited excellent reusability after five cycles owing to its 3D macro structure.

Harnessing the power of polyethyleneimine in modifying chitosan surfaces for efficient anion dyes and hexavalent chromium removal

In this investigation, synthesis of a surface-functionalized chitosan known as amino-rich chitosan (ARCH) was achieved by successful modification of chitosan by polyethyleneimine (PEI). The synthesized ARCH was characterized by a specific surface area of 8.35 m2 g−1 and a microporous structure, with pore sizes predominantly under 25 nm. The Zeta potential of ARCH maintained a strong positive charge across a wide pH range of 3–11. These characteristics contribute to its high adsorption efficiency in aqueous solutions, demonstrated by its application in removing various anionic dyes, including erioglaucine disodium salt (EDS), methyl orange (MO), amaranth (ART), tartrazine (TTZ), and hexavalent chromium ions (Cr(VI)). The adsorption capacities (Qe) for these contaminants were measured at 1301.15 mg g−1 for EDS, 1025.45 mg g−1 for MO, 940.72 mg g−1 for ART, 732.96 mg g−1 for TTZ, and 350.15 mg g−1 for Cr(VI). A significant observation was the rapid attainment of adsorption equilibrium, occurring within 10 min for ARCH. The adsorption behavior was well-described by the Pseudo-second-order and Langmuir models. Thermodynamic studies indicated that the adsorption process is spontaneous and endothermic in nature. Additionally, an increase in temperature was found to enhance the adsorption capacity of ARCH. The material demonstrated robust stability and selective adsorption capabilities in varied conditions, including different organic compounds, pH environments, sodium salt presence, and in the face of interfering ions. After five cycles of adsorption, ARCH maintained about 60% of its initial adsorption capacity. Due to its efficient adsorption performance, simple synthesis process, low biological toxicity, and cost-effectiveness, ARCH is a promising candidate for future water treatment technologies.

A Comparative study on the Removal of different dyes from aqueous medium using Zinc Ferrite Nanocomposite and Rice Husk Adsorbents

This research aimed to develop simple, inexpensive, and ecologically suitable adsorbents for removing dyes through adsorption. Thus, co-precipitation and in-situ polymerization techniques were utilised to produce polyaniline resulting in the synthesis of Zinc Ferrite Polyaniline Nanocomposite (ZF-PANI NC). Also, Rice Husk (RH) was also used as adsorbent. Scanning electron microscope (SEM) and x-ray diffraction (XRD) experiments were carried out on ZF nanoparticles and ZF-PANI NC. The average grain size of ZF-PANI NC was 13 nm. When compared to RH that had been treated with sodium hydroxide (SHRH), RH seemed more crystalline. However, the crystalline nature of SHRH was slightly enhanced by the adsorptive Reactive Yellow (RY) dye, and the surface of SHRH appears uniform in the SEM images. Rhodamine B (RhB) dye adsorbance’s at known concentrations were measured using a UV–visible spectrophotometer and a calibration curve. Percent removal of RhB dye by ZF-PANI NC over time (0–45 min) and in the presence of various adsorbent doses (0.1–0.5 g) revealed that the percentage of dye removal rose when ZF-PANI NC dose was increased. At room temperature (25 °C), RY dye adsorption on RH and SHRH revealed only 65 % in 40 min, whereas SHRH removed 99 %. ZF-PANI NC was suitable as a reliable and affordable adsorbent for dye remediation from aqueous solution. SHRH and RH both performed better in adsorbing RY dye. A pseudo-2nd order kinetic approach with the Langmuir adsorption isotherm provided the best fit for the results. The low value of ΔG° demonstrated the viability of RY adsorption. SHRH and ZF-PANI NC have high adsorption efficiency compared to RH and ZF.

Novel high-efficient adsorbent based on modified gelatin/montmorillonite nanocomposite for removal of malachite green dye

Shortage of drinking water has gained potential interest over the last few decades. Discharged industrial effluent, including various toxic pollutants, to water surfaces is one of the most serious environmental issues. The adsorption technique has become a widely studied method for the removal of toxic pollutants, specifically synthetic dyes, from wastewater due to its cost-effectiveness, high selectivity, and ease of operation. In this study, a novel gelatin-crosslinked-poly(acrylamide-co-itaconic acid)/montmorillonite (MMT) nanoclay nanocomposites-based adsorbent has been prepared for removing malachite green (MG) dye from an aqueous solution. Modified gelatin nanocomposites were synthesized using a free-radical polymerization technique in the presence and absence of MMT. Various analytical instrumentation: including FTIR, FESEM, XRD, and TEM techniques were used to elucidate the chemical structure and surface morphology of the prepared samples. Using a batch adsorption experiment, Langmuir isotherm model showed that the prepared modified gelatin nanocomposite had a maximum adsorption capacity of 950.5 mg/g using 350 mg/L of MG dye at pH 9 within 45 min. Furthermore, the regeneration study showed good recyclability for the obtained nanocomposite through four consecutive reusable cycles. Therefore, the fabricated gelatin nanocomposite is an attractive adsorbent for MG dye elimination from aqueous solutions.

Performance and mechanism of graphene oxide removal from aqueous solutions by calcite: adsorption isotherms, thermodynamics, and kinetics.

The flow of graphene oxide (GO) into natural water systems can adversely affect water environments and ecosystems. In this study, the adsorption effect of calcite on GO under different conditions was studied using calcite as adsorbent. Meanwhile, characterized by a combination of microscopic experiments, including SEM, TEM, XRD, FTIR, Raman, XPS, and AFM, additional research on the performance and the mechanism of GO sorption by calcite was conducted. The findings indicated that the highest adsorption efficiency was observed at a temperature of 303 K, pH 3, a mass of 90 mg of calcite, with an initial concentration of 60 mg L-1 GO, resulting in a 95% adsorption rate. The adsorption isotherm conformed to the model of Langmuir and Temkin, and it is a heat absorption process dominated by monolayer adsorption. The thermodynamic analysis showed that the adsorption was spontaneous and heat-absorbing. The adsorption kinetics conformed to the pseudo-second-order kinetic model, and the sorption procedure is chemisorption. In conclusion, calcite has a good sorption capacity for GO, which can provide a reference for the removal of GO in the aqueous environment.

Construction of C8/threonine-functionalized mesoporous silica aerogel based on mixed-mode and its adsorption properties for both anionic and cationic dyes

High adsorption and desorption efficiencies for both anionic and cationic dyes are still a challenge for adsorbents to treat dyestuffs wastewater. In this study, the C8/threonine-functionalized mesoporous silica aerogel based on mixed-mode was constructed to overcome the challenge, with properties of hydrophobicity and switchable surface charge of n-octyl and threonine groups. With methylene blue and azophloxine as cationic and anionic dye models, batch tests were conducted. The consequences proofed the adsorption process was efficient and fast, and the highest adsorption quantities for methylene blue and azophloxine were estimated as 274.30 mg/g and 152.43 mg/g, respectively. Additionally, the adsorbent showed good removal efficiency and reusability. The desorption efficiencies exceeded 97% using low concentration HCl or NaOH as eluents. Mechanism investigation proved that adsorption process relied on hydrophobicity and electrostatic interactions. These results instructed that SG-C8/Thr was a promising adsorbent with excellent adsorption and desorption efficiencies for both anionic and cationic dyes.

Arsenic bioremediation in mining wastewater by controllable genetically modified bacteria with biochar

Arsenic (As) is a highly toxic chemical element associated with cardiovascular diseases and diabetes. Using genetically modified microorganisms (GMOs) for arsenic detoxification or removal is taking center stage in recent years. However, the bio-safety issue of GMOs remains an obstacle. In this study, we proposed a bioremediation process to efficiently adsorb arsenic from mining wastewater by combining a controllable GMO with biochar. One metagenomic gene element (ArsR) with high arsenic adsorption efficiency was newly identified from mining wastewater environment. Then the gene was chromosomally integrated into strain Pseudomonas putida KT2440, which is a widely used strain for environmental bioremediation. The growth-regulation genetic circuit coordinating suicide gene expression was deployed onto the genome of strain KT2440. This non-auxotrophic, antibiotic-free and self-controlled programmable circuit was fine-tuned with highly sensitive perceptibility towards arsenic levels below wastewater discharge standard (< 0.50 mg/L), which made the system applicable. A biochar-microorganism coupled recovery strategy was further implemented in mining wastewater treatment, leading to increased arsenic removal capacities, which is ready for use under a circumstance up to 20 mg/L of total arsenic pollution. No more than 1.32 × 10−9 escapee of GMOs was observed in the process, which meets the US NIH guidelines for GMOs release (<10−8). Thus, this study demonstrated the feasibility for arsenic bioremediation by GMOs in industrial wastewater.

Adsorption of Copper and Cadmium from Wastewater Using Chemically Activated Watermelon Peels as Adsorbent

Activated Carbon of high adsorption efficiency and highly active surface properties were prepared from water melon fruits peels by using 1M H2SO4 solution, followed by activation at 300oC for 30 minutes. The adsorption capacity of the activated carbon is considered on the following; the effect of concentration, adsorbent dosage, and contact time. The physicochemical characteristics such as ash content (18.7%), pH(6.72),moisture content (1.82), bulk density(0.36) and conductivity (32.4) were investigated to understand the adsorptive capacity of activated carbon prepared from water melon peels. The adsorptive efficiency of the adsorbent in removing Cadmium and Copper ions from wastewater were compared with Langmuir and Freundlich adsorption isotherm, which proved effective removal efficiency within the range of 91.80 – 99.98 %. On the whole chemically activated watermelon peels should be used in treating our wastewaters, for a cleaner and healthier environment.

Exploring the potential of waste biomass of olive as an additive for layered double hydroxide/polyurethane as an effective and safe agent for the adsorption of drug residues: a bioremediation approach

O-Pom-LDH-PU composite demonstrates high efficiency in cefotaxime adsorption, showing low cytotoxicity, and strong antibacterial activity, presenting a cost-effective, green solution for wastewater treatment, and promising green chemistry potential.

Avaliação do potencial de adsorção de rejeitos de mineração de ferro e seu efeito na germinação de raphanus sativus

ABSTRACT The objective of this work was to evaluate the physicochemical and adsorptive characterization of Fe tailing collected in the district of Brumadinho; and verify its effect on Raphanus sativus germination. The material was collected on the surface layer (0-20 cm) and disintegrated for pH, redox potential – Eh, electrical conductivity – EC, OM, cation exchange capacity – CEC, specific surface area – SSA and functional groups characterization. Adsorption studies were conducted using methylene blue (MB). The results of the adsorption studies were analyzed using kinetic models (Elovich, pseudo-first order – PFO and pseudo-second order – PSO) and isotherm models (Freundlich, Langmuir and Sips). The tailing has an acidic pH (5.60), negative ΔpH (-0.30) and low CEC (1.85 cmolc g-1). A high MB adsorption efficiency (96%) was verified. The Elovich model (0.9248&lt;R2&lt;0.9858) best represented the chemical kinetics, and the Freundlich model best describes the MB adsorption process in the tailing (R2 = 0.9609). The maximum adsorption capacity (qm) was equal to 15.08 mg g-1. The presence of Fe tailing positively influenced the germination of R. sativus seeds (73.8%), but stem and root growth were inferior when compared to seedlings cultivated in compost substrate. It is concluded that the material has favorable cationic adsorption capacity, which can benefit soil fertilization. However, R. sativus development was minor in Fe tailing substrate, probably due to low CEC, OM and nutrient availability.

Fabrication of bimetallic MOF-74 derived materials for high-efficiency adsorption of iodine.

Owing to their high porosity, open metal sites, and huge surface area, metal-organic framework (MOF) materials are commonly employed in iodine adsorption processes. Bimetallic MOFs have drawn a lot of attention since mono-metal MOFs have been unable to keep up with the demand. Bimetallic MOF materials still have drawbacks, including limited adsorption capacity, extended adsorption time, poor stability, and poor selectivity, despite their positive performance in radioactive iodine capture. It has been therefore difficult to develop adsorbents with quick iodine adsorption rates and high iodine adsorption efficiency. This study investigated the adsorption properties of a series of bimetallic MOF-74 materials (Mn-Co-MOF-74, Mn-Zn-MOF-74, and Mn-Ni-MOF-74) for radioactive iodine, as well as their design and synthesis utilizing the reflux approach. It was discovered that the adsorption performance of Mn-Ni-MOF-74 for radioiodine was superior to that of the other two bimetallic MOF-74 materials. Using the bimetallic Mn-Ni-MOF-74 as a precursor, a variety of bimetallic MOF-74 derived carbon compounds (Mn-Ni-CX) were prepared by high-temperature pyrolysis. Simultaneously, the structure of the material and the iodine adsorption characteristics have been thoroughly studied.