Magnetic Alginate Research Articles

Effect of Structurally Different Magnetic Alginate Nanocomposite Beads on Fenton-Like Oxidation of Direct Dyes

Effect of Structurally Different Magnetic Alginate Nanocomposite Beads on Fenton-Like Oxidation of Direct Dyes

Efficient multifunctional PPy-NTs/PEI@alginate@NiFe2O4 magnetic beads for heavy metals removal: Experimental design and optimization interpretations

A highly effective magnetic nanocomposite alginate beads (PPy-NTs/PEI@Alg@NiFe2O4) were synthesized using alginate as the encapsulation reagent and polypyrrole/polyethylene imine with nano NiFe2O4 as a functional filler to remove toxic Zn2+ and Pb2+ from polluted water. A response surface methodology (RSM) was used to statistically assess the influences of pH and the adsorbent dose on the adsorption performance. PPy-NTs/PEI@Alg@NiFe2O4 magnetic microbeads exhibited the optimal adsorption capacity qe (18.6 mg/g) at pH 6 and a 2 mg/L dose for Zn2+ removal. In comparison, the optimal qe (32.6 mg/g) was reached at pH 4.5 with a 1.5 mg/L dose for Pb2+ remediation. From batch experiments, maximal absorption capacities of 53.3 mg/g and 22 mg/g were achieved for Pb2+ and Zn2+, respectively, at 313 K. The pseudo-second-order kinetic model fitted the results well, suggesting that the chemisorption process regulates adsorption. Isotherm models indicate the presence of homogeneous adsorption sites from the well-fitting to Langmuir isotherm. An investigation of the effects of temperature and thermodynamic considerations revealed the endothermic nature of Zn2+ and Pb2+ absorption. The Fourier transform infrared spectra showed that –NH, –NH2, and –COO− are the main groups in PPy-NTs/PEI@Alg@NiFe2O4 composite beads that were responsible for Zn2+ and Pb2+ removal from polluted water.

Inkjet-based facile fabrication of a copper ferrocyanide-embedded magnetic alginate microadsorbent for highly enhanced cesium removal

For the first time, simple and facile fabrication of a magnetic alginate microadsorbent via piezoelectric inkjet technology was developed for the selective removal of 137Cs via magnetic separation. Through the ejection of an alginate solution containing potassium ferrocyanide and magnetic nanoparticles (MNPs) into a Cu2+ solution via an inkjet device, the fabrication of a copper ferrocyanide-embedded magnetic alginate microadsorbent (CuFC-MAM) with an average size of 39.38 μm was easily achieved in a one-pot fabrication process; here, the Cu2+ ions acted as both a cross-linker for the gelation of alginate and a Cu source for the in situ synthesis of CuFC with potassium ferrocyanide. The Cs adsorption behavior of CuFC-MAM was effectively fitted by the pseudo-second-order kinetic model and Langmuir isotherm. Owing to the increased specific surface area of CuFC-MAM, its pseudo-second-order rate constant and maximum adsorption capacity were 76.54 and 1.486 times greater than those of CuFC-embedded magnetic alginate macroadsorbents fabricated without inkjet devices. Compared with other Cs adsorbents, CuFC-MAM presented the highest maximum capacity and Kd value; these results were attributed to the high content of CuFC in CuFC-MAM (50.15%). In addition, our CuFC-MAM exhibited an excellent removal efficiency of radioactive Cs, exceeding 99% from seawater.

Magnetic alginate microrobots with dual-motion patterns through centrifugally driven flow control

Mobile microrobots have gained increasing attention in biomedical applications because they can be precisely actuated to targeted positions in a tiny space. However, their use in biomedical applications is hindered by the costly and complicated fabrication method. Herein, a facile fabrication method is proposed to produce magnetic alginate microrobots with adjustable dimensions, including teardrop and tadpole shapes, via tunable centrifugally-driven flows. The formation of these microrobots is interpreted by finite element analysis, revealing that the transition between the dripping and jetting regimes of the flow alters the microrobot's shape. The dimensions of the microrobots are quantitatively analyzed based on the flow's extrusion velocity, controlled by nozzle diameters and revolution speeds. Incorporating magnetic nanoparticles into the alginate-based hydrogel enables the microrobots to exhibit distinct motion patterns under a magnetic field. The teardrop-like microrobot can reach a maximum rolling velocity of approximately 2.7 body length s−1 at 2 Hz, while the maximum stick-slip velocity of the tadpole-like microrobot reaches about 0.42 body length s−1 at 5 Hz, comparable to the existing bioinspired magnetic microrobots. These two motion patterns allow the microrobot to overcome obstacles and navigate in vertically constrained environments, respectively. Last, an ultrasound imaging system is deployed to monitor the locomotion and degradation of the microrobots, showing their potential for targeted drug delivery applications.

One-step synthesis of superparamagnetic copper alginate gel microspheres (Cu2+-Alg@Fe3O4) using a compression nebulizer

For the application needs of histidine-rich protein separation, this study proposes to prepare a magnetic adsorbent enriched with copper ions and small particle size. Using a compression nebulizer, the magnetic + sodium alginate solution was broken into micrometer-sized droplets and cross-linked and cured with copper ion solution. The magnetic copper alginate microspheres (Cu2+-Alg@Fe3O4) were obtained with an average particle size of 7.1 μm, a magnetic saturation intensity of 36.9 emu·g−1, and a Cu2+ content of 149.2 mg·g−1.The adsorption equilibrium time of the Cu2+-Alg@Fe3O4 microspheres on bovine hemoglobin(BHb) was 90 min, and the maximum adsorption amount was 4318.5 mg·g−1. The Cu2+-Alg@Fe3O4 microspheres also showed stable and good adsorption performance in five cyclic adsorption experiments.

Magnetic alginate core-shell nanoparticles based on Schiff-base imine bonding for pH-responsive doxorubicin delivery system

This research describes the development of a novel pH-responsive drug delivery system (DDS) based on sodium alginate (SA) and magnetic nanoparticles (MNPs) for cancer treatments. One possible approach to creating a wide variety of functional nanoparticles is to graft functional materials onto magnetite nanoparticles. In this study, we demonstrate the effective alteration of Fe3O4 nanoparticles using the alginate dialdehyde (ADA) group through a Schiff-Base imine reaction toward synthesizing Fe3O4@SiO2@APTMS@ADA (FSA@ADA) nanocarrier (NC). doxorubicin (DOX) as an anticancer drug was loaded (about 93 % drug loading capacities) on the FSA@ADA NC through chemical and physical interactions. doxorubicin (DOX) as an anticancer drug was loaded (about 93 % drug loading capacities) on the FSA@ADA NC through chemical and physical interactions. The synthesized nanocarriers were thoroughly characterized by various techniques, including FT-IR, FE-SEM, EDX-MAP, TEM, XRD, VSM, TGA, and 1HNMR. In vitro DOX release studies showed a pH-dependent manner and its release rate is lower (< 15 %) at 7.4 than pH 5 (about 75 %) over 25 days. Cytotoxicity results showed good biocompatibility for blank FSA@ADA (over about 85 % cell viability), whereas DOX-loaded FSA@ADA NCs had higher cytotoxic effects (IC50 value: ∼6 µg/mL) as a result of the controlled release of DOX into HeLa cells. Results showed that the magnetic core-shell FSA@ADA/DOX NC has the potential to be used as a targeted stimuli-responsive drug for cancer treatment.

Agmatine ligand functionalized magnetic alginate beads for removal of U(VI) ions from solution

In the presented work, magnetic alginate (MA) beads were prepared and activated with epichlorohydrin and then functionalized with agmatine ligands (MA-A). The materials were analyzed by FTIR, SEM, XRD, and BET methods. The adsorption capacity of the MA-A for U(VI) was 451.4 mg/g. The Langmuir isotherm model well described the experimental data for the adsorption of U(VI) ions. The second-order kinetic model data proposed that the adsorption of U(VI) ions preferred the chemisorption mechanism. The adsorption enthalpy of the MA-A beads for U(VI) ions was 35.4 kJ/mol. After seven cycles of use, the adsorption capacity of MA-A beads was not significantly changed for U(VI) ions. Finally, the functionalization of MA beads with agmatine ligand can be a good candidate for applications for environmental technologies to remove metal ions.

Immobilization of Coprinus comatus with magnetic alginate hydrogel microsphere for improving the antioxidant activity of fermentation products

Coprinus comatus is an edible mushroom and its fermented product possesses antioxidant activity. In this study, to further enhance the antioxidant activity and improve the reusability of the strain, calcium alginate hydrogel was used as the carrier for embedding and immobilizing Coprinus comatus. The effects of CaCl2 concentration, sodium alginate concentration, microsphere diameter, and the amount of magnetic particle on the antioxidant activity of fermented products were investigated. The results showed that the magnetic immobilized microsphere prepared by 2.50% CaCl2, 2.00% sodium alginate and 0.50% Fe3O4 had the best fermentation antioxidant activity (EC50 was 0.43 ± 0.01 mg/mL) when the diameter was 5 mm, which increased by 24.56% compared to the initial activity. Besides, the microsphere showed strong reusability, the antioxidant activity was still better than the free strain after being used five times. This study not only enhanced the antioxidant activity of Coprinus comatus fermented product through immobilization, but also provided an effective method for microbial fermentation.

Magnetic alginate supported potassium manganese ferrocyanide for the recovery of uranium from acidic wastewater

Abstract With the rapid development of the atomic energy industry, the demand for nuclear fuel has risen, while the limited resources of uranium mines make it difficult to meet the needs of the future development of nuclear energy. Expanding sources of uranium acquisition is necessary, and the enrichment and recovery of precious uranium from uranium-containing wastewater is invaluable. By synthesizing alginate supported potassium manganese ferrocyanide nanocomposites with magnetic response (KMnFC/MA/Fe3O4), the high efficiency adsorption and separation of uranium in acidic uranium-containing wastewater can be realized conveniently and quickly. The magnetic composite was characterized by a variety of technical means, and the adsorption behavior of the magnetic material on uranium was studied by static adsorption experiments under different environmental conditions. The adsorption kinetics and isotherm of uranium by KMnFC/MA/Fe3O4 were studied by using some common linear adsorption models. The results show that the adsorption rate of KMnFC/MA/Fe3O4 on uranium is fast, and the adsorption equilibrium can be reached within 90 min. The adsorption process conforms to a pseudo-secondary kinetic model and is dominated by chemisorption. The adsorption of uranium by KMnFC/MA/Fe3O4 magnetic material is single molecular layer adsorption, and the maximum adsorption capacity is 425.5 mg g−1 at 35 °C. KMnFC/MA/Fe3O4 is a promising adsorbent in the field of acidic low-concentration uranium wastewater treatment because of its good effect on the treatment of low concentration uranium wastewater, the concentration of uranium in the wastewater reaches the emission standard after treatment and it is easy to be separated magnetically after adsorption.

Injectable Magnetic Hydrogel Filler for Synergistic Bone Tumor Hyperthermia Chemotherapy.

The therapeutic efficacy of bone tumor treatment is primarily limited by inadequate tumor resection, resulting in recurrence and metastasis, as well as the deep location of tumors. Herein, an injectable doxorubicin (DOX)-loaded magnetic alginate hydrogel (DOX@MAH) was developed to evaluate the efficacy of an alternating magnetic field (AMF)-responsive, chemothermal synergistic therapy for multimodality treatment of bone tumors. The prepared hydrogel exhibits a superior drug-loading capacity and a continuous DOX release. This multifunctionality can be attributed to the combined use of DOX for chemotherapy and iron oxide nanoparticle-containing alginate hydrogels as magnetic hyperthermia agents to generate hyperthermia for tumor elimination without the limit on penetration depth. Moreover, the hydrogel can be formed when in contact with the calcium ions, which are abundant in bone tissues; therefore, this hydrogel could perfectly fit the bone defects caused by the surgical removal of the bone tumor tissue, and the hydrogel could tightly attach the surgical margin of the bone to realize a high efficacy residual tumor tissue elimination treated by chemothermal synergistic therapy. The hydrogel demonstrates excellent hyperthermia performance, as evidenced by in vitro cytotoxicity tests on tumor cells. These tests reveal that the combined therapy based on DOX@MAH under AMF significantly induces cell death compared to single magnetic hyperthermia or chemotherapy. In vivo antitumor effects in tumor-bearing mice demonstrate that DOX@MAH injection at the tumor site effectively inhibits tumor growth and leads to tumor necrosis. This work not only establishes an effective DOX@MAH system as a synergistic chemothermal therapy platform for treating bone tumors but also sheds light on the application of alginate to combine calcium ions of the bone to treat bone defect diseases.

In-situ magnetic alginate coated chitosan core@shell beads with excellent performance in simulated and real wastewater treatment: Behavior, mechanisms, and new perspectives

Herein, a new hybrid magnetic core@shell biocomposite was prepared based on an alginate-bentonite core and a chitosan shell layer (mAB@Cs) where magnetic Fe3O4 NPs (50.7 nm) were in-situ generated on the surface via a simple non-thermal co-precipitation approach. The biocomposite has a high ability to magnetically separate and remove organic (ciprofloxacin (CPX)) and seven toxic inorganic (Cu2+, Cd2+, Co2+, Ni2+, Pb2+, Zn2+, and Hg2+) contaminants from simulated wastewater. Experimental results showed a CPX monolayer chemisorption with a Langmuir maximum adsorption capacity of 264.7 mg/g, maintained effectiveness up to the fifth cycle, and high removal rates of heavy metals ranging from 74.89 % to 99.86 % corresponding to adsorption capacities ranging from 12 to 20 mg/g. For a more accurate evaluation, the biocomposite was tested on a real urban wastewater sample (RWW) and it has manifested a noteworthy efficiency in removing a mixture of inorganic pollutants in terms of potassium K+ and orthophosphate phosphorous P-PO43−, and organic matter in terms of biological oxygen demand (BOD) and chemical oxygen demand (COD) with 46 %, 90 %, 84 %, and 64 % removal efficiencies, respectively. On top of this, a high inactivation rate of E. coli of the order of 96 % was recorded, making the prepared magnetic biocomposite adept for the simultaneous removal of emergent wastewater pollutants, from organic, inorganic, to pathogen microorganisms.

Efficient removal of aqueous Pb(II) ions by magnetic alginate composite microcapsules containing canola straw‐derived biochar as the reinforcing fillers

AbstractWith the rapid development of industry, water pollution caused by lead has caused great harm to human health. In this study, alginate is used as a base and blended with biochar to form calcium alginate hydrogel beads with high mechanical properties through ionic cross‐linking. Besides, the material (BC/MCAC) is prepared by the material (C‐γ‐Fe2O3) as a magnetizing agent and to remove lead. Then, a series of batch experiments and material characterizations are performed to evaluate the adsorption process of the material. The results show that the maximum adsorption capacity of BC/MCAC to Pb(II) is 211.6 mg g−1 at pH = 7. The adsorption process is well described by the Langmuir adsorption isotherm and pseudo‐second‐order kinetic model. This indicates that the lead adsorbed by BC/MCAC is a monolayer chemisorption that occurs on a uniform surface. After three regeneration cycles, BC/MCAC is found to retain 82.37% of the lead adsorption capacity and has good regeneration ability. Lead is removed by BC/MCAC mainly through the complexation of oxygen‐containing functional groups, electrostatic interaction, and ion exchange. BC/MCAC allows for more sustainable use of the wastes and is expected to be a new type of lead adsorbent for industrial wastewater.

Phosphate-functionalized magnetic calcium alginate for the engineering remediation of uranium-contaminated water and soil

The increasingly hazardous and radioactive environmental issues arising from the uranium-contaminated water and soil make it urgent to develop high-yield and efficient adsorbents and the green engineering remediation technology, as well as the engineering remediation evaluation. In this work, we successfully synthesis a phosphate-functionalized magnetic calcium alginate hydrogel (MPCA) in batches by using a simple in-situ coprecipitation method. MPCA keeps maximum adsorption proportion of uranium (≥60.01 %) in the mixed multi-nuclide solution, and high adsorption capacity in different natural simulated uranium-contaminated water systems. In the engineering remediation of natural uranium-contaminated soil, MPCA removes 83.9 % of uranium and 99.8 % of radium in muddy water, even removes 92.9 % of uranium in the soil leaching wastewater. This work also validates a promising green engineering linked soil remediation technology, which combines soil leaching and adsorption separation. The remediated soil meets international emission standards, 92.9 % of uranium in the leachate is removed, 93.2 % of adsorbed uranium is desorbed and enriched. In addition, the reuse of adsorbed leachate and desorbed MPCA also minimize the consumption of engineering water and the derived radioactive water pollution.

Removal of lead and cadmium ions from wastewater using magnetic alginate impregnated sulfur

A new adsorbent, magnetic Fe3O4 sulfonated nanoparticle caged alginate microbeads (S.MNPs@Alg), was developed for Cd(II) and Pb(II) ions removal from water, which could be effectively separated from the solution owing to the superparamagnetic property. This adsorbent was characterized using FTIR, FESEM, XRD, SEM, and VSM. The effect of parameters affecting sorption potential including pH, contact time, and adsorbent dosage was carried out. Under the best experimental condition, the Cd(II) and Pb(II) ions removal efficiencies were reported to be over 95%. To understand the nature of the sorption process, adsorption isotherms including Freundlich and Langmuir models were precisely investigated. The process is fitted well with the Langmuir model and the maximum adsorption capacity obtained was 37 mg. g−1 and 85 mg. g−1 for Cd(II) and Pb(II) ions, respectively. The as-prepared S.MNPs@Alg is easy to prepare and effective in the uptake of Cd(II) and Pb(II) ions with a physisorption mechanism, which adsorption rate is limited with the pseudo-second-order model. The adsorbent lost<5% of its removal efficiency in five adsorption–desorption cycles. Finally, the existence of sulfur groups increased adsorption capacity and decrease the toxicity of magnetic nanoparticles (MNPs) and the presence of magnetism part can facilitate the separation of the adsorbent from the solution.

High-Throughput Generation, Manipulation, and Degradation of Magnetic Nanoparticleladen Alginate Core-shell Beads for Single Bacteria Culturing Analysis.

Microbes could be found almost everywhere around us and have significant impacts on our human society. The treatment of microorganisms has long been seen as a complex problem. Till now, most of the genetic and phenotypic information regarding rare species is buried in the bulk microbial colony due to a lack of efficient tools to screen live bacteria. Droplet microfluidics offers a powerful approach to address this problem. However, the interactions among bacteria and their living environment are entirely restricted by the water/oil interfaces in conventional water/oil single emulsion-based microfluidic systems. Here, we demonstrate an oil-mediated all-aqueous microfluidic workflow that can overcome this drawback. In contrast to the previous works, our all-aqueous culturing environment allows cell-cell and cell-environment interactions, thus facilitating the growth of bacteria. Fe3O4 magnetic nanoparticles added into the alginate beads enables on-chip manipulation of the microcapsules. The core-shell structure separately encapsulates bacteria and magnetic particles in the core and shell to avoid contamination. We demonstrate the feasibility of this approach by single bacterium culturing in droplet-templated alginate beads. Finally, a new approach is proposed to degrade the alginate beads for post-treatment. This novel microfluidic workflow can create new opportunities for microbial applications, such as bacteria culturing and screening.

The use of immobilised bacteria cross-linked within magnetic alginate beads enhances the treatment of benzophenone-type UV filter chemicals by the SBR system

Benzophenone-n compounds (BPs) are applied in a broad spectrum of commercial products, one of which is sunscreen. These chemicals are frequently detected in a variety of environmental matrices worldwide, especially water bodies. BPs are defined as emerging contaminants as well as endocrine-disrupting contaminants; thus, it has become necessary to develop aggressive and green treatments to remove BPs. In this study, we used immobilised BP-biodegrading bacteria linked to reusable magnetic alginate beads (MABs). The MABs were added to a sequencing batch reactor (SBR) system to enhance the removal of 2,4-dihydroxybenzophenone (BP-1) and oxybenzone (BP-3) from sewage. The BP-1 and BP-3 biodegrading bacteria in the MABs consisted of strains from up to three genera to allow for efficient biodegradation. The strains used were Pseudomonas spp., Gordonia sp., and Rhodococcus sp. The optimal composition of the MABs consisted of 3% (w/v) alginate and 10% (w/v) magnetite. The MABs resulted in 60.8%–81.7% recovery by weight after 28 days, and there was a continuous release of bacteria. Moreover, the biological treatment of the BPs sewage improved after adding 100 g of BP1-MABs (1:27) and also 100 g BP3-MABs (1:27) into the SBR system at a hydraulic retention time (HRT) of 8 h. Compared with the SBR system without MABs, the removal rates of BP-1 and BP-3 increased from 64.2% to 71.5% and from 78.1% to 84.1%, respectively. Furthermore, the COD removal increased from 36.1% to 42.1%, and total nitrogen increased from 30.5% to 33.2%. Total phosphorus remained constant at 29%. The bacterial community analysis showed that the Pseudomonas population was <2% before the MAB addition, but increased to 56.1% by day 14. In contrast, the Gordonia sp. And Rhodococcus sp. Populations (<2%) remained unchanged throughout the 14-day treatment period.

Size Tunable Fabrication of Magnetic Alginate Microparticles Using Flow Focusing Microfluidics

AbstractThe size tunable formulation of magnetic alginate microparticles (MAMs) using a 3D flow‐focusing microfluidic device is reported. The droplet phase consists of iron oxide nanoparticles (IONPs) in an alginate solution and the continuous phase consists of fluorocarbon oils. The stability of IONP colloids in alginate and calcium ethylenediamine tetraacetic acid solutions using optical microscopy, dynamic light scattering, and zeta potential measurements is studied. These studies suggest that IONPs coated with polyethylene glycol (PEG) are most stable. MAMs using the PEG‐coated IONP colloid are then formulated and it is studied how MAM the average size and coefficient of variance vary as a function of droplet and continuous phase flow rates and viscosities. Droplet and MAM size decrease when the carrier flow rate or viscosity increases, and droplet and MAM size increase when droplet flow rate or viscosity increases. Crosslinking and drying of droplets result in MAMs whose diameter is ≈44% less than the original droplets while maintaining a population coefficient of variance below 8%. Conditions are identified that enable fabrication of MAMs with diameters between 30 and 60 µm with coefficients of variance of ≈6–7%. These results may guide future work exploring the role of MAM size on various applications.

Nd Recovery from Wastewater with Magnetic Calcium Alginate ((1,4)-β-d-Mannuronic Acid and α-L-Guluronic Acid) Hydrogels.

In this study, a magnetic adsorbent material was produced, by environmentally friendly and inexpensive precursor materials, to clean wastewater that may result from primary and secondary rare earth metal (REM) production. Then, the absorption of Nd3+ ions from wastewater was done and this process's kinetic and isotherm models were developed. Thus, the removal of Nd3+ from wastewater with magnetic materials was accomplished, and then, this precious metal was recovered by using different acid media. First, Fe sub-micron particles were successfully produced by the polyol method. To increase the stability of Fe-based particles, their surfaces were covered with an oxide layer, and the average thickness was determined as 16 nm. The synthesized Fe particles were added into the calcium alginate beads and then coated with chitosan to increase the pH stability of the gels. The chemical composition of the gels was determined by Fourier transform infrared spectroscopy, the thermal properties were determined by differential scanning calorimetry, and the magnetic properties were determined by vibrating-sample magnetometer analysis. The magnetic saturation of the hydrogels was 0.297 emu/g. After the production of magnetic calcium alginate hydrogels, Nd3+ ion removal from wastewater was done. Wastewater was cleaned with 94.22% efficiency. The kinetic models of the adsorption study were derived, and isotherm studies were done. Adsorption reaction fitted different kinetic models at different time intervals and the Freundlich isotherm model. The effect of pH, temperature, and solid-liquid ratio on the system was determined and the thermodynamic constants of the system were calculated. After the adsorption studies, Nd3+ ions were regenerated in different acid environments and achieved an 87.48% efficiency value. The removal of Nd3+ ions from wastewater was carried out with high efficiency, the gels obtained as a result of adsorption were regenerated with high efficiency by using acid media, and it was predicted that the gels could be reused. This study is thought to have reference results not only for the removal of REM from wastewater by magnetic adsorption materials but also for the adsorption of heavy metals from wastewater.

Magnetic alginate–carboxymethyl cellulose to immobilize copper nanoparticles as a green and sustainable catalyst for 4-nitrophenol reduction

In the present work, sustainable green catalysts with high activity, and excellent stability were prepared and thoroughly characterized by XRD, FT-IR, BET, VSM, SEM, EDX, HR-TEM, and TGA techniques. The combined sodium alginate (SA) and carboxymethyl cellulose (CMC) biopolymers were functionalized with Fe3O4 nanoparticles to immobilize copper nanoparticles to form Fe3O4@SA–CMC–CuNP nanocomposites in batch experiments. Furthermore, the Fe3O4@SA–CMC–CuNP nanocomposites were utilized as the heterogeneous catalyst for 4-nitrophenol (4-NP) reduction to 4-aminophenol (4-AP) in the presence of NaBH4, and the progress of the catalytic reaction was monitored using UV–visible spectrophotometry. The Fe3O4@SA–CMC–CuNP nanocomposite exhibited much higher catalytic activity for the 4-nitrophenol reduction reaction than individual components Fe3O4 and Fe3O4@SA–CMC. The effect of parameters such as the amount of catalyst was evaluated and 30 mg of the catalyst amount with a 95.0% reduction of 4-nitrophenol for 1.5 min was obtained. The effect of reaction temperature was also investigated to find out the activation energy. The analyses of kinetics and thermodynamics were carried out to understand the catalytic behavior. Furthermore, the catalyst can be separated from the reaction system through the usage of a magnet and recycled up to five times without any loss of activity. Therefore, the development of sustainable green catalyst biopolymer-based nanocomposites is promising for new catalysts in the future for treating organic wastewater.

Cyclodextrin-functionalized magnetic alginate microspheres for synchronous removal of lead and bisphenol a from contaminated soil

Currently, functional materials-based soil remediation focused on the stabilization of heavy metals and organics to inhibit their migration, however, the possible second release of these pollutants caused by soil condition variation attracts broad attention. Herein, β-cyclodextrin functionalized magnetic sodium alginate microspheres (MSA-CDMW) were fast and facilely synthesized through microwave-assisted one-pot method for synchronous detachment of Pb and BPA from contaminated soil. The obtained MSA-CDMW presented wide pH adaptability and fast capture for Pb(II)/BPA with superior adsorption capacity of 369.03/165.37 mg/g. Furthermore, the effects of material dosage and soil pH on the remediation ability of MSA-CDMW were explored in detail. After adding 5% MSA-CDMW into the contaminated soil for 3-round successive remediation (12 h for each round), the amount of extractable Pb and total BPA was simultaneously decreased by 56.30 and 0.78 mg/kg, respectively. Meanwhile, the quantity of exchangeable and carbonate bound Pb was significantly decreased to 7.13% with transformation into relatively stable fractions. A series of characterizations revealed that ion exchange, pore filling, complexation, and electrostatic attraction were responsible for Pb binding, while MSA-CDMW could capture BPA through host-guest interaction by the hydrophobic cavity of β-cyclodextrin. Additionally, recovery and floatation results revealed that the MSA-CDMW could be easily separated from the soil using magnets even at extreme drying and wetting conditions, thus providing a novel, fast, and eco-friendly strategy for effective remediation of heavy metals and organics contaminated soil.