Efficient Sorbent Research Articles

Insights into the performance and mechanism of a reinforced lignocellulosic sorbent fabricated from sawdust biomass for multi-tasking application in enrofloxacin removal and monitoring

Natural lignocellulose-based materials have numerous strengths such as abundance, cheap price and biodegradability, which indicates a brilliant prospect for environmental protection. This work aimed to design an efficient sorbent (NaSS-PSD) by pine sawdust (PSD) for the surveillance and management of enrofloxacin (ENR). In the study, sodium styrenesulfonate (NaSS) was chosen as an effective monomer to ameliorate the performance of PSD by graft copolymerization. The removal of ENR by NaSS-PSD was enhanced in comparison with the ungrafted ones under investigated conditions. Pseudo-second-order and Temkin were the best-fitted models to describe the adsorption behavior. For the first time, NaSS-PSD was employed as a novel extractant of solid-phase extraction (SPE) and dispersive solid-phase microextraction (DSPME) to develop accurate, eco-friendly and economic analytical techniques for trace ENR determination. Good linearity and reproducibility were obtained. The limits of detection were 0.41 μg/L for DSPME-HPLC-DAD technique and 0.15 μg/L for SPE-HPLC-DAD technique. These two methods exhibited satisfying practicability when applied to quantify ENR residue in real waters. The study on interfacial interaction mechanism and preferential binding sites suggested that hydrogen bond and π-π interactions took the primary responsibility. Our work provides a good perspective for tailoring natural lignocellulosic biomass to be alternative adsorbents for emerging pollutants.

An ecofriendly pectin-co-montmorillonite composite hydrogel for the separation of contaminant metal ions from water

The aim of this study was to investigate the synthesis, characterization, and sorption performance of ecofriendly pectin-co-montmorillonite composite hydrogels for the separation of potentially toxic elements (PTEs) from water. Hydrogels were synthesized using an environmentally friendly method, incorporating montmorillonite (MMT) at proportions ranging from 0 to 10 % in the tridimensional pectin (PC) network. The composite hydrogels were characterized by Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Batch sorption studies were conducted to investigate the capacity to separate copper (Cu2+), nickel (Ni2+), manganese (Mn2+), zinc (Zn2+), cadmium (Cd2+), and hexavalent chromium (Cr6+) ions from water. Higher PTE separation efficiencies were found with hydrogels containing 1 % MMT, with greater selectivity for Cu2+ ions. An exhaustive sorption study revealed that the separation process of Cu2+ fits the pseudo-second-order kinetic model and Langmuir isotherm, with maximum sorption capacity (qmax) of ~36.8 mg of hydrogel per g of PTE. This indicates that PC-co-MMT composite hydrogels are efficient alternative sorbents for the selective separation of PTEs from water, with potential application in ecofriendly water purification systems.

Engineered Mg-modified biochar-based sorbent for arsenic separation and pre-concentration

The utilization of biochar as a relatively efficient sorbent or stationary phase for the separation and preconcentration of a wide range of analytes represents an innovative approach in current sample pretreatment methods. Appropriate pre- and post-pyrolysis modification of the input precursor and pyrolysis product, respectively, allows targeted design of the physicochemical properties and sorption characteristics of the resulting sorbent. The present work deals with the preparation of pyrolysis materials based on unmodified cattail leaf biomass (BC) and its Mg-modified analogue (MgBC) by a slow pyrolysis process at 500 °C and a residence time of 1 h in a pyrolysis reactor. Physicochemical characterization of BC and MgBC carried out by pH, total C, N, surface size analysis (SSA), 13C NMR, SEM-EDX and XRD confirmed significant morphological and mineralogical differences between the prepared sorbents. By performing sorption experiments using a model anionic analyte (As) and application of Langmuir isotherm, we found that the predicted maximum sorption capacity of MgBC for As is 13.5-fold higher than that of BC. The sorption process of As by both sorbents is best described by the Sips adsorption isotherm (R2 ≥ 0.995) and a pseudo-nth order kinetic model (R2 ≥ 0.997). The optimum pH for As sorption by BC and MgBC sorbents is in the interval 5–6. The presence of competitive phosphate anions (equimolar concentration of 1:1) in the solution significantly reduces the sorption capacity of MgBC for As by 40% for BC by 70%. The presence of Cl- ions showed no significant effect on the sorption capacity of Bc and MgBC for As. Both sorbents were best recovered using 0.1 mol/L NaOH solution when the desorption efficiency for both sorbents was more than 95%. The MgBC sorbent showed 35% retention of As from the real sample in the model SPE column at a flow rate of 0.12 mL/s. Based on the obtained knowledge, it is evident that biochar-based sorbent prepared from Mg-modified precursor represents an effective sorbent for anionic forms of analytes and opens the possibility of its use also in preconcentration and separation techniques.

Efficient Selective CO2 Composite Sorbent from Amino Acid Ionic Liquids and Silica Gel: 2H NMR Spectroscopy Provides Insight on the CO2-Binding Mechanism and in-Pore Microscopic Viscosity.

A promising CO2 sorbent based on the [Emim][Gly] (1-ethyl-3-methylimidazolium glycinate)/silica gel composite has been studied. CO2 sorption experiments have shown that the optimum loading of [Emim][Gly] ionic liquid in silica gel is 40 wt.%. The 2-step process CO2 binding mechanism in [Emim][Gly] has been proposed based on the results of sorption experiments, 2H NMR spectroscopy and ab-initio calculations. The impact of CO2 on the microscopic viscosity and the dynamical melting of ionic liquid has been thoroughly investigated. 2H NMR spectroscopy has revealed that CO2 strongly binds cation and anion in [Emim][Gly], forcing them to move in a correlated fashion.

A Natural Carbon Encapsulated in Gellan-Based Hydrogel Particles Designed for Environmental Challenges.

This article reports the obtention of a new gellan-based hydrogel linked with Fe3+ and loaded with a natural micro/nanostructured carbon designed as a contaminant's removal from wastewater. Hydrogels are known for their water-retaining properties, high binding capacity, and eco-friendly features. The new material is expected to behave as one cost-effective and efficient sorbent, including natural carbon structures with various functional groups. The encapsulation efficiency ranges between 89% and 95%. The obtained hydrogel particles were characterized using FT-IR spectroscopy and scanning electron microscopy techniques. The hydrogel particles' water stability was evaluated by measuring the transmittance for 10 days, and the capacity to retain water was assessed by determining the swelling degree (Q%). The results showed that hydrogel particles are stable (the transmittance value is higher than 97.8% after 10 days), and their properties are influenced by the cross-linking degree, the amount of the carbon particles encapsulated, and the concentration of gellan. For example, the Q% values and encapsulation efficiency increased when the cross-linking degree, the carbon microstructure quantity, and the gellan concentration decreased. The new hybrid material can retain Pb(II) ions and diclofenac molecules, and could be used in different adsorption-desorption cycles.

Synthesis of Functionalized Pyridine Modified Magnetic Nanoparticles for Utilization in Magnetic Solid-Phase Extraction of Tebuconazole and Propiconazole Followed by Quantification via High-Performance Liquid Chromatography-Ultraviolet Detection.

In the current study, a new magnetic sorbent (Fe3O4@2,6-diamino-4-(3,4-dihydroxyphenyl) pyridine-3,5-dicarbonitrile) was prepared as a new and efficient sorbent to be used in the magnetic solid-phase extraction method to extract tebuconazole and propiconazole as model compounds. In this regard, effective parameters such as pH of the sample solution, desorption volume, ionic strength, extraction time, desorption time, and amount of the magnetic sorbent were optimized using experimental design. In the optimal condition, the linear dynamic ranges for tebuconazole and propiconazole were between 0.5 and 200.0µg/L. Also, the limits of detection, limits of quantification, and relative standard deviations were 0.21-0.14µg/L, 0.49-0.45µg/L, and 1.3%-4.6%, respectively. The estimated enrichment factors for tebuconazole and propiconazole were 22 and 28, respectively. The absolute recovery (AR%) values for tebuconazole and propiconazole were also 67% and 84%, respectively. Finally, the proposed method was used for determination of tebuconazole and propiconazole in cucumber, tomato, orange, and lemon fruits. The obtained result confirmed that the presented method is capable for the analysis of the selected analytes in complicated matrices. In addition, the ARs% were in the range of 67%-84%. The result proved that the presented method can be an alternative to the extraction process of various pesticides.

Surfactant-modified carbon nano-onion-β-cyclodextrin nanocomposite as an efficient sorbent in dispersive solid phase extraction of metoprolol and atenolol from plasma samples prior to HPLC–PDA analysis

Surfactant-modified carbon nano-onion-β-cyclodextrin nanocomposite as an efficient sorbent in dispersive solid phase extraction of metoprolol and atenolol from plasma samples prior to HPLC–PDA analysis

Honeycomb-like porous carbons derived from multistep pyrolysis of artificial humic acids as efficient sorbents for removing diethyl phthalate

The uprecycling of hydrothermal liquid waste-derived artificial humic acids into stable carbon materials is helpful for advancing the development of hydrothermal carbonization technology, but it has rarely been investigated. For the first time, a multistep pyrolysis method was designed to convert artificial humic acids into honeycomb-like porous carbons (PCs). The obtained PCs exhibited a high specific surface area, reaching 1728.55 m2/g, while nonactivation treatment still provided a high value of 1425.14 m2/g. The hightemperature pyrolysis process yielded graphite-like structures and maintained surface functional groups. PCs have been applied as sorbents to remove the emerging plasticizer diethyl phthalate (DEP) in water environments and exhibit promising sorption capabilities (as high as 993.30 mg/g), which are much higher than those reported for other sorbents. The sorption rate was controlled by mass transfer and chemical-like sorption, whereas the sorption capability was controlled mainly by the adsorption process, especially pore filling. Partitioning, hydrogen bonding, pore filling and π–π stacking are possible sorption mechanisms. In addition to the specific surface area, the pore volume is a suitable parameter for assessing the sorption capability. Exogenous dissolved organic matter can affect the sorption of DEP onto PCs through cosorption and coverage of their surface, but its influence is limited. Excellent sorption performance can cover a wide range of pH conditions. The prepared PCs also showed notable reusability and practicality. In this study, an excellent method was proposed for recycling hydrothermal liquid waste and preparing PCs, and the prepared PCs exhibited great potential for environmental remediation.

Exploring the potential of Desert Rose fibers (Adenium obesum) for the remediation of oil-contaminated sites

This work proposes the use of Fibers from the pod of Desert Rose, Adenium obesum (DRF), as an alternative for oil removal in spill scenarios and cleaning of contaminated bird feathers. The sorption capacity of biomass was evaluated through kinetics tests, which were adjusted using the Fractal Linear Driving Force (FL-LDF) model. Additionally, capture stability tests were performed to determine the oil retention capacity of the material. Furthermore, the DRF were tested in the cleaning of bird feathers, and the fibers were characterized using Optical Microscopy (OM), SEM, FTIR and TGA. The DRF demonstrated sorption efficiency, with approximately 13.01 ± 1.87 g/g, 14.59 ± 0.58 g/g and 49.12 ± 2.43 g/g, for diesel oils, 20 W50 mineral oil and petroleum, respectively. It was found that these results were achieved by combining the viscosity with the functional groups identified on the material surface, which strongly contributed to the sorption capacity. The sorption kinetics indicated a fast rate in the first minute of testing for diesel oils and 20 W50. The material was still stable, managing to retain 65 %, 83 % and 78 % and removing from the feathers a total of 82 %, 71 % and 81 % of diesel oils, 20 W50 and petroleum. The biomass presented a hollow cylindrical structure, with the presence of grooves and roughness in some regions of its surface with a thin wall, demonstrating to be an efficient and competitive oil sorbent.

Ultra-efficient removal of aqueous hexavalent chromium by activated biochar nanoparticles derived from squid ink

Biochar have been recognized as efficient and renewable carbon sorbents, which attracted much attention on Cr contamination remediation in wastewater. In this study, we propose a cost-effective one-step strategy to synthesize activated biochar nanoparticles derived from squid ink (AS-BC) for aqueous Cr(VI) removal. The results demonstrated that AS-BC achieved a removal rate of 24.29 h−1 at 700 °C (400-times higher than the unmodified one). This was also a state-of-the-art removal performance for aqueous Cr(VI) compared to other reported materials. AS-BC possessed an enormous specific surface (2408 m2/g at 700 °C) with abundant O- and N-containing groups, condensed aromatic structures, and high electron transfer capacity (3.64 and 2.13 mmol e−/g for EAC and EDC at 700 °C), contributing to the ultra-efficient removal of Cr(VI) by synergistic adsorption and reduction. AS-BC absorbed Cr(VI) in the form of HCrO4− by electrostatic attraction with protonated amine-N and hydroxy (-NH3+ and -OH2+) groups and Cr(III) in the form of Cr3+ by complexation with amine-N and hydroxy groups. With a hydroxy-quinone and conjugated π-electron system, AS-BC served as mediator and shuttle to accelerate electron transfer in Cr(VI) reduction with an electron donor. Therefore, our findings highlight the immense potential of AS-BC biochar nanoparticles represent a potential alternative for high-performance Cr(VI) remediation in wastewater.

Laser-synthesized TiN-based nanoparticles as novel efficient electrostatic nanosorbent for environmental water cleaning

Abstract Dyes used in industries such as textile, paper, and leather are known to be harmful to both human health and aquatic ecosystems, which makes critically important the search of effective and sustainable methods for their removal from wastewater in order to mitigate the detrimental pollution effects. Here, we show that titanium nitride nanoparticles (TiN NPs) synthesized by scalable methods of pulsed laser ablation in liquid ambient (water, acetone and acetonitrile) can serve as extremely efficient sorbents for water decontamination from dye molecules (methylene blue, crystal violet, and malachite green). Our tests show that adsorption of TiN NPs is associated with the electrostatic effect due to a strong negative charge of laser-synthesized TiN NPs and the presence of pores in the NPs. Comprehensive characterization using scanning and transmission electron microscopy, along with Raman spectroscopy, evidenced that the appearance of surface charge is related to the formation of under-stoichiometric TiN (TiN1-x), associated with the predominance of nitrogen vacancies. This study identifies an optimal configuration of vacancy defects that maximizes dye adsorption, with TiN NPs synthesized in water exhibiting superior performance, achieving a dye sorption capacity of 136.5 mg/g at room temperature for methylene blue, which corresponds to best earlier reported values for nanomaterials. This study not only extends the utility of TiN NPs to environmental remediation but also highlights the critical influence of synthesis conditions on their functional properties, offering a pathway towards the design of more effective materials for pollution control.

Removal of aflatoxin M1 in milk using magnetic laccase/MoS2/chitosan nanocomposite as an efficient sorbent

The current study tries to find the impact of the integration of laccase enzyme (Lac) onto magnetized chitosan (Cs) nanoparticles composed of molybdenum disulfide (MoS2 NPs) (Fe3O4/Cs/MoS2/Lac NPs) on the removal of AFM1 in milk samples. The Fe3O4/Cs/MoS2/Lac NPs were characterized by FT-IR, XRD, BET, TEM, FESEM, EDS, PSA, and VSM analysis. The cytotoxic activity of the synthesized nanoparticles in different concentrations was evaluated using the MTT method. The results show that the synthesized nanoparticles don't have cytotoxic activity at concentrations less than 20 mg/l. The ability of the prepared nanoparticles to remove AFM1 was compared by bare laccase enzyme, MoS2, and Fe3O4/Cs/MoS2 composite, indicating that the Fe3O4/Cs/MoS2/Lac NPs the highest adsorption efficiency toward AFM1. Besides, the immobilization efficiency of laccase with a concentration range of 0.5–2.0 was investigated, indicating that the highest activity recovery of 96.8% was obtained using 2 mg/ml laccase loading capacity. The highest removal percentage of AFM1 (68.5%) in the milk samples was obtained by the Fe3O4/Cs/MoS2/Lac NPs at a contact time of 1 h. As a result, Fe3O4/MoS2/Cs/Lac NPs can potentially be utilized as an effective sorbent with high capacity and selectivity to remove AFM1 from milk samples.

Frontiers in environmental cleanup: Recent advances in remediation of emerging pollutants from soil and water

Recent advancements in environmental remediation have significantly improved the treatment of soil and water pollution, yet the complexity and dispersion of emerging pollutants remain major challenges. This review highlights the most promising technologies and strategies in remediation emphasizing their potential to protect ecosystems and human health. In soil remediation, phytoremediation utilizes plants to absorb and immobilize pollutants while bioremediation employs microorganisms to degrade organic contaminants in a sustainable manner. Nanotechnology offers innovative solutions through the use of nanoparticles as efficient sorbents or catalysts. For water remediation, advanced oxidation processes (AOPs) such as photocatalysis and ozonation effectively degrade recalcitrant pollutants enhancing water quality. Biochar and other sorbents present viable options for pollutant removal and membrane technologies like reverse osmosis provide selective purification for diverse applications. The review underscores the importance of multidisciplinary collaboration in advancing remediation technologies. Integrating artificial intelligence and machine learning can further optimize these processes by analyzing complex data and predicting pollutant behavior. As environmental challenges evolve, continuous innovation and research are essential to combat emerging pollutants. This review serves as a call to action for the scientific community to embrace interdisciplinary approaches and cutting-edge technologies to safeguard the environment for future generations.

The N,N,N′,N′-tetraphenylbenzidine-based conjugated hypercrosslinked polymers for adsorping iodine and fluorescence sensing 2,4-dinitrophenol, iodine

Although progress has been made in the development of hypercrosslinked polymers (HCPs) for iodine uptake, their fluorescence performance and fluorescence sensing performance are rare due to the lack of conjugated behavior in common HCPs. Herein, the N,N,N′,N′-tetraphenylbenzidine-based conjugated hyper-crosslinked polymers (conjugated TPB-based HCPs) were efficiently fabricated via a one-step Friedel-Crafts arylation reaction by selecting N,N,N′,N′-tetraphenylbenzidine (TPB) and N,N′-diphenyl-N,N′-di(m-tolyl)benzidine (DPDB) as the basic building blocks and p-dimethoxybenzene (DMB) as an external crosslinker which will lead to the formation of the conjugated structures. The derived TPB-based HCPs (denoted as, TPB-DMB and DPDB-DMB) possessed excellent stability and high surface areas, Their iodine adsorption capacities are up to 4.25 and 3.56 g·g−1. The high iodine adsorption is caused by chemical adsorption. The fully conjugated structure and the 3D aryl network give the conjugated TPB-based HCPs excellent luminescence properties and fluorescence sensing properties for 2,4-dinitrophenol and iodine. The fluorescence sensing mechanisms of the conjugated TPB-based HCPs for DNP and I2 includes photo-induced electron process and the resonance energy transfer process. This study provides a viable approach for the development of highly efficient iodine sorbents and fluorescence sensors of DNP and iodine for addressing environmental issues.

Melt-blown polypropylene nonwoven as an efficient and eco-economic sorbent for pipette tip micro-solid phase extraction for the determination of tyrosine kinase inhibitors

BackgroundThe detection of tyrosine kinase inhibitors (TKIs) in biological fluids is essential due to their critical role in cancer therapy and the variability in individual drug metabolism, which necessitates precise dosing. Traditional methods for analyzing TKIs in biological fluids, such as blood plasma, typically involve complex sample preparation techniques that can be resource-intensive, environmentally burdensome, and not sufficiently sensitive for low-concentration analytes. There is a pressing need for more efficient, economical, and environmentally friendly methods that can enhance sensitivity and throughput without compromising accuracy. ResultsThis study explores the use of melt-blown polypropylene nonwoven (MBPP), commonly found in face masks, as a novel sorbent for pipette-tip micro-solid phase extraction (PT-μSPE). MBPP demonstrated excellent hydrophobicity and significant mesoporous adsorption capacity. An extraction device was fashioned by inserting a segment of MBPP (15 mg) into a 200 μL disposable plastic pipette tip, which was then attached to a 2.5 mL disposable plastic syringe. The MBPP's fabric form removes the need for a frit, allowing the extraction process to be completed in just 3 min through simple plunger manipulation. The method achieved extraction recoveries ranging from 60.5 % to nearly 100 %. Subsequent method validation using liquid chromatography-tandem mass spectrometry (LC-MS/MS) showed satisfactory linearity (coefficient of determination R2 > 0.993), accuracy (relative recoveries: 86.3%–114.8 %), and precision (relative standard deviation: 3.4%–11.3 %), with detection limits between 0.022 and 0.135 ng mL−1. SignificanceThe introduction of MBPP for PT-μSPE represents a significant advancement in the bioanalytical detection of TKIs, offering a highly efficient, cost-effective, and environmentally sustainable method. It compares favorably with existing techniques, offering advantages in terms of cost, environmental impact, and ease of use. This approach has the potential to be widely adopted for routine monitoring of TKIs in clinical settings.

Oyster shell facilitates the green production of nitrogen-doped porous biochar from macroalgae: a case study for removing atrazine from water

Low-cost and green preparation of efficient sorbents is critical to the removal of organic contaminants during water treatment. In this study, the co-pyrolysis of macroalgae and oyster shell was designed to synthesize nitrogen-doped porous biochars for sorption removal of atrazine from water. Oyster shell played a significant role in opening pores in macroalgae-derived biochars, resulting in the surface area of the macroalgae (Enteromorpha prolifera and Ulva lactuca) and oyster shell co-pyrolyzed carbonaceous as high as 1501.80 m2 g−1 and 1067.18 m2 g−1, the pore volume reached 1.04 cm3 g−1 and 0.93 cm3 g−1, and O/C decreased to 0.09 and 0.08, respectively. The sorption capacity of atrazine to nitrogen-doped porous biochars (the Enteromorpha prolifera, Ulva lactuca and oyster shell co-pyrolyzed carbonaceous) reached 312.06 mg g−1 and 340.52 mg g−1. Pore-filling, hydrogen bonding, π-π or p-π stacking and electrostatic interaction dominated the multilayer sorption process. Moreover, the nitrogen-doped porous biochars showed great performance in cyclic reusability, and the Enteromorpha prolifera, Ulva lactuca and oyster shell co-pyrolyzed carbonaceous sorption capacity still reached 246.13 mg g−1 and 255.97 mg g−1, respectively. Thus, this study suggested that it is feasible and efficient to remove organic contaminants with the nitrogen-doped porous biochars co-pyrolyzed from macroalgae and oyster shell, providing a potential green resource utilization of aquatic wastes for environmental remediation.Graphical

Separation of Nd(III) from Nd(III)/Co(II) Mixture Using Poly (Carboxymethyl Cellulose.starch-g-acrylic Acid/Al2O3) Nanocomposite

AbstractThe separation of neodymium from the Nd(III)/Co(II) mixture is crucial for producing high-purity neodymium, which is essential in industries like electronics. A new nanocomposite, Poly(carboxymethyl cellulose.starch-g-acrylic acid/Al2O3), P(CMC-St-g-AA/Al2O3), was prepared and applied for the sorption and separation of Nd(III) from the Nd(III)/Co(II) mixture. This nanocomposite, synthesized with γ-irradiation of 60Co at 35 kGy, was extensively characterized using SEM, FTIR spectroscopy, and TGA-DTA. Parameters affecting neodymium separation were studied, revealing optimal conditions. Kinetic experiments showed agreement with a pseudo-nth-order kinetic model. Isothermal sorption studies indicated multilayer adsorption, with Co(II) and Nd(III) adsorption capacities of 2.781 mg/g and 8.825 mg/g, respectively, at pH 3.0. Thermodynamic analysis confirmed spontaneous and endothermic sorption. Separation factor values peaked at pH 3.0, shaking for 120 min, 0.1 adsorbent dosage, and ambient temperature, highlighting effective Nd-Co separation under these conditions. In conclusion, the comprehensive analysis and successful application of P(CMC-St-g-AA/Al2O3) nanocomposite underscore its potential as a highly efficient and selective sorbent for neodymium separation.

Magnetic biochar conjugated quaternary ammonium salt-constructed hemoperfusion adsorbent for viral removal with rapid and high-performance

Due to variations in virus structures and their high variability, treating viral infections remains challenging. Moreover, developing vaccines and medications for newly emerged viruses demands a significant time investment. Efficient methods are required to prevent dangerous infections caused by unknown pathogens. Hemoperfusion, with its low cost, can effectively remove toxins from the blood quickly, thus achieving therapeutic effects. The core of the hemoperfusion technology lies in the adsorbent. Therefore, the development of a viral adsorbent aiming to combat viruses through hemoperfusion was envisioned, following general principles to effectively save lives and buy time for the research and development of vaccines and medications. Towards this goal, a facile, green, and low-priced magnetic biochar/quaternary ammonium salt (Fe3O4/C-2) was constructed using the hydrothermal carbonization (HTC) method. HIV lentiviruses were used as a model pathogen to quantify the adsorption capacity and elucidate the adsorption mechanism. Benefiting from a macroporous structure and electrostatic interactions, fabricated Fe3O4/C-2 has a high adsorption capacity (965 ng g−1) and strong suppression of infectious activity (99.99%). Moreover, a low hemolysis ratio (<2%), high cell viability (>100%), high activated partial thromboplastin time (APTT) (67.29 s), and low protein adsorption (<5%) indicate outstanding biocompatibility and good anticoagulant activity. Therefore, Fe3O4/C-2 is expected to serve as a simple and efficient pathogen sorbent for viral diseases treatment.

Sorption behavior of strontium and europium ions from aqueous solutions using fabricated inorganic sorbent based on talc

Sorption of Sr(II) and Eu(III) from aqueous solutions was studied using tin molybdate talc sorbent synthesized by the precipitation technique. The synthesized sorbent was characterized using different analytical tools, such as; FT-IR, SEM, XRD, XRF, TGA, and DTA. The sorption studies applied to Sr(II) and Eu(III) include the effects of shaking time, pH, concentrations, and saturation capacity. The sorption of Sr(II) and Eu(III) depends on pH, reaction kinetics obey the pseudo-2nd-order model, and the Langmuir model is better suited for the sorption isotherm. The thermodynamic parameters reflect an endothermic and spontaneous sorption process. Desorption studies showed that 0.1 M HCl was the best desorbing agent for the complete recovery of Sr(II) (96.8%) and Eu(III) (92.9%). Finally, the obtained data illustrates that the synthesized sorbent can be applied and used as an efficient sorbent for the sorption of Sr(II) and Eu(III) from aqueous solutions and can be used as a promising sorbent to remove Sr(II) and Eu(III).

Thermodynamic and CO2 sorption investigations on improved Li3BO3-based sorbents by NaOH addition

The development of new solid sorbents with high carbon capture capacity and good reversible sorption properties is considered a key factor for mitigating CO2 emissions. Tri-lithium borate (Li3BO3) has shown to be a high-capacity CO2 sorbent adequate for an intermediate temperature range (500–650 °C). However, the performance of this sorbent has been little studied in particular at low CO2 concentrations, requiring the introduction of changes in Li3BO3 to make it competitive. Here, highly efficient NaOH-modified Li3BO3 sorbents were synthesized by a simple two-step mechano-thermal method at low temperature using different amounts of NaOH. For the first time, the influence of increasing amounts of an additive on the standard enthalpy change of Li3BO3 as well as on the relation between CO2 pressure and temperature equilibrium was determined. A progressive rise in the standard enthalpy change and a decrease in the equilibrium CO2 pressure at a fixed temperature were observed with the increase in the amount of additive. Moreover, the NaOH addition to Li3BO3 improves its CO2 capture capacity, CO2 absorption rate and stability during carbonation/regeneration cycles. The CO2 capture capacity ranges between 50 wt% and 35 wt% at pure CO2 and 15 % CO2, respectively, for low amounts of NaOH added. Further studies showed that CO2 capture/desorption efficiency is kept high after 20 cycles at 525 °C and 15 % CO2. The improved performance of NaOH-modified Li3BO3 sorbents and the changes in the thermodynamic properties were associated with two factors: the partial substitution of boron by carbon in the Li3BO3 structure, and the formation of Li2CO3-Na2CO3 molten carbonates. Therefore, these NaOH-modified Li3BO3 materials represent attractive CO2 sorbents for moderate temperatures, applicable for post-combustion industrial processes.