Excellent Adsorption Properties Research Articles

Effective adsorptive removal of heavy metal anion Cr(Ⅵ) and dye cation methylene blue by the novel 2D material TiVCTx MXene

With the increasingly serious industrial pollution, the effective removal of heavy metal ions and organic pollutants from wastewater has become a key issue of environmental protection. In this paper, a new MXene material, TiVCTx, was prepared by in situ etching, and its adsorption capacity of heavy metal anion Cr(Ⅵ) and methylene blue (MB) dye cation was studied. The effect of adsorption time, pH values, temperatures, initial concentrations of adsorbent and adsorbate, interfering ions on the Cr(Ⅵ) and MB adsorption of TiVCTx was systematically investigated. It is found that TiVCTx has excellent Cr(Ⅵ) and MB adsorption property, the adsorption capacity can be as high as 600mg/g and 1430mg/g, respectively. The adsorption experiments revealed that the adsorption process of Cr(Ⅵ) conformed to the Langmuir isotherm model and the Pseudo-second-order kinetic model, which indicated that the Cr(Ⅵ) adsorption was a heat-absorbing monolayer chemisorption. In contrast, the adsorption process of MB is in accordance with the Freundlich isotherm model and the Pseudo-second-order kinetic model, suggesting that the MB adsorption was an exothermic multilayer chemisorption. The results of X-ray electron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) analysis further confirmed that the reductive adsorption and electrostatic adsorption can account for the outstanding Cr(VI) and MB adsorption capacity of TiVCTx, respectively.

PVA-enhanced green synthesis of CMC-based lithium adsorption films

The titanium-based lithium ion sieve (HTO), renowned for its exceptional adsorption performance and cyclic stability, was utilized in addressing the global shortage of lithium resources. However, the recovery and reuse efficiency of HTO in powder form is relatively low, which limits its application in industrial fields. To address this issue, this study utilized carboxymethyl cellulose (CMC) as the principal matrix material, while polyvinyl alcohol (PVA) played a dual function as both matrix and crosslinker, negating the necessity for supplementary crosslinking materials. Employing water as the only solvent, HTO was embedded into the CMC-PVA blended film matrix. It was observed that augmenting the CMC content substantially elevates the adsorptive capability of the film. However, this enhancement comes at the cost of reduced mechanical robustness and diminished stability in solution. Consequently, by balancing the influence of adsorptive capacity and stability through fine-tuning the CMC-to-PVA ratio. Even when HTO powder is encapsulated within the film, the adsorption film retains the excellent adsorption properties of HTO, achieving an adsorption capacity for lithium of 29.21 mg g−1 within 12 h. This study provides an innovative pathway and ideas for the large-scale, low-cost production of sustainable lithium-ion adsorption materials.

Preparation of Loess‐Clay Based Eco‐Friendly Geopolymer for Efficient Removal of Pollutants in Water

AbstractHeavy metals and dyes cause serious harm for water environment, geopolymer materials with the large pores and specific surface area, and easy modification of pore surface have received extensive attention in wastewater treatment. Herein, using loess‐clay (LC) as natural mineral materials, we developed an eco‐friendly geopolymer of loess‐clay (GpLC) with excellent adsorption properties and promotion plant growth was prepared by alkali excitement. Its morphology and structure were exhibited by scanning electron microscopy, Fourier transform infrared spectroscopy, XRD, and Brunauer–Emmett–Teller. Moreover, its adsorption property for removing metal ions and different dyes was measured, and the adsorption kinetics and thermodynamics were investigated. GpLC presented excellent adsorption ability for Pb2+, which the removal rate got to 98.7 %. It had the universality of removing organic pollutants, and the removal rate reached to 98.0 %. It was dominated chemisorption and single‐layer adsorption, which GpLC conformed to quasi‐second‐order adsorption kinetics, and being more consistent with Langmuir isothermal model. Furthermore, it was found that GpLC could promote growth of crops as it contain P and K element with essential element of plants. In summary, it provides insights and strategy for developing a kind of eco‐friendly functional materials with strong adsorption capacity and promoting plant growth, and it is an effective method for reusing loess resources.

New solid phase microextraction fibers with green clay coating via radio frequency magnetron sputtering for detecting low-polar compounds in water samples

BackgroundDeveloping highly sensitive and selective measurement techniques to detect trace compounds in diverse matrices is a significant challenge in analytical chemistry. These techniques must adhere to green chemistry principles by minimizing organic solvent use, simplifying sample preparation, and streamlining process steps. Additionally, there is a growing need for sustainable analytical methods due to increased environmental awareness. The problem addressed in this work is the need for an eco-friendly and efficient method for the extraction and detection of trace organochlorine pesticides in water samples. ResultsWe employed SPME using a novel clay thin film sorbent, deposited on a nickel-titanium alloy wire via magnetron sputtering. Montmorillonite clay was chosen for its excellent adsorption properties and eco-friendly nature, aligning with green chemistry principles. The approach involved coating the SPME fiber with hydrophobic modified montmorillonite clay, followed by silylation. The method was tested for extracting 12 model organochlorine pesticides, including BHC, lindane, and DDT, demonstrating high isolation efficiency. The coated thin film and its silylation modification were characterized using standard spectroscopic techniques, confirming the successful creation of a new adsorbent phase. The direct immersion SPME approach achieved relative recoveries ranging from 65 % to 99 %, with reproducibility (RSD) below 6 %. This method provided low detection limits (10–15 ng L−1) and quantitation limits (32–50 ng L−1). SignificanceOur approach offers an eco-friendly, highly efficient solution for the extraction and detection of trace organochlorine pesticides. The significant improvement in recovery rates and reproducibility, combined with low detection and quantitation limits, underscores the potential of this method to enhance analytical practices in environmental monitoring and public health. Furthermore, the use of sustainable materials and processes aligns with global efforts to reduce environmental impact in analytical chemistry.

SERS Sensor for Acetylcholine Detection Based on Covalent Organic Framework Hybridized Gold Nanoparticles As Nanozymes.

An innovative and potent nanozyme with reductase-like activity was developed by integrating the in situ synthesis of gold nanoparticles (Au NPs) onto the surface of a covalent organic framework (COF). Based on the reductase-like activity of the COF-hybridized Au NPs, this nanozyme could efficiently catalyze the reduction of 4-nitrophenol (4-NPH). Moreover, the prepared nanohybrid was utilized as an excellent surface-enhanced Raman scattering (SERS) substrate for highly sensitive SERS detection by combining the excellent adsorption properties of COFs and the large number of Raman hotspots between the high-density Au NPs. For the first time, 4-NPH was used as an SERS marker to detect the electron receptor acetylcholine (Ach), with high sensitivity; Ach acted as an inhibitor in this catalytic reaction. The linear range of Ach was 1.0 pM to 10 nM, the correlation coefficient was 0.993, the detection limit was approximately 0.3 pM with a signal-to-noise ratio (s/n) of 3, and the acceptable recovery in the serum was 97.2% to 104.5%. The results from this study show that the nanozyme-SERS system has great potential for chemical and bioassay applications.

Development of modified MgO/biochar composite for chemical adsorption enhancement to cleanup fluoride-contaminated groundwater

Fluoride contamination in groundwater has become a global environmental issue. Magnesium oxide (MgO) has demonstrated effectiveness as an adsorbent in treating fluoride pollution in groundwater. However, its use in powder and fine granular form often results in losses during the adsorption process, posing challenges for post-treatment recovery and potentially causing secondary environmental pollution. In this study, two novel fluoride adsorbents [rice husk (RH) and spent coffee grounds (SCG)-based magnesium oxide (MgO) biochar composites (MgO/RH and MgO/SCG)] were developed to cleanup fluoride-polluted groundwater. During the adsorbent synthesis process, RH and SCG biochar were pyrolyzed at 500 °C and modified by calcination using MgO. Both MgO/RH and MgO/SCG surfaces exhibited abundant pore structures and formed MgO crystal phases. Batch experiments results show that when the MgO/RH and MgO/SCG material dosages were 1 g/L, fluoride removal rates reached 80% and 86% respectively. The isotherms and kinetics of fluoride adsorption with MgO/RH and MgO/SCG followed the Langmuir isotherm equation and pseudo-second-order kinetic model. The maximum fluoride adsorption capacities of MgO/RH and MgO/SCG were 63.47 mg/g and 141.98 mg/g, respectively, indicating these materials used mono-layer adsorption mechanism for fluoride adsorption. The addition of MgO into the pores of porous adsorbent materials effectively increased their reactive sites and enhanced the adsorption performance of carbon materials. Particularly, SCG biochar had a richer pore structure than RH biochar, providing a larger contact surface area, facilitating the effective dispersion and doping of MgO into the pores. Therefore, MgO/SCG composite exhibited excellent fluoride adsorption properties in water, indicating the potential for developing a new type of MgO-modified SCG adsorbent material with green prospects. This composite effectively mitigated fluoride contamination, reducing the fluoride concentration in groundwater. Both RH and SCG are agricultural and food waste by-products, thus offering the opportunity to significantly reduce production, operation, and maintenance costs.

Microwave-treated layered graphite for highly efficient solar-powered seawater desalination and wastewater treatment

In the midst of the global water crisis, the ‘waste-to-treasure’ strategy, which includes desalination and wastewater recycling, is proving to be a promising approach. However, existing solar evaporators are hampered by challenges such as low photothermal conversion efficiency and significant heat losses. Here, we present an innovative solution that reduces the band gap of the material and improves the efficiency of light recycling. As a result, the microwave-treated graphite achieves a 15 % reduction in reflectivity and a 9 °C increase in surface temperature. In addition, the integration of this graphite with a hydrogel to modulate the interfacial wettability further optimizes the evaporation efficiency. When exposed to sunlight, the developed cone column evaporator achieves an impressive evaporation rate of 2.91 kg m−2 h−1, which is a significant increase of 663 % over the natural evaporation rate of a 3.5 wt% NaCl solution. Remarkably, no salt deposits were observed on the surface of the evaporator during the tests and the material exhibited excellent adsorption and desorption properties for pollutants, highlighting its potential for sustainable applications. These results provide valuable theoretical and practical insights for the design and development of high-efficiency solar evaporators.

Reusable superhydrophobic fluorinated cellulose-graphene composite aerogels for selective oil absorption

Although some progress had been made in the adsorption of graphene aerogels, more research was needed on their elasticity and recyclability. In this paper, a superhydrophobic fluorinated cellulose and graphene composite aerogel (FCGA) was prepared by a simple two-step impregnation method. Firstly, nano-cellulose was introduced into the graphene aerogel to inhibit the excessive accumulation of graphene lamellae and increase the specific surface area. The surface of the composite aerogel was then impregnated with silanol and fluorinated functional groups by a two-step impregnation method, resulting in a superhydrophobic aerogel with remarkable elasticity. The introduction of cellulose and silane provided the aerogel with excellent elasticity and recovery from cyclic adsorption. The successful grafting of the fluorophobic groups of PFDMS onto the graphene oxide strengthened the framework of the graphene aerogel, making FCGA a good candidate for repeated selective oil absorption. It could be restored to the original height after compression to 50% and 80% strain decompression. FCGA could efficiently absorb oil in water and had a high organic adsorption capacity. And the adsorption capacity of different oils/organic solvents reached 22,480 mg/g∼36,700 mg/g. Its absorption efficiency remained above 98.5% under distillation cycles. Due to its high elasticity, it retained more than 90% of its cyclic adsorption capacity through the squeeze cycle. As a simple, low-cost recovery method, its reusability was already better than most known adsorption elastic materials. The prepared composite aerogel had the advantages of simple preparation, low density (0.014 g/cm3), superhydrophobicity (water contact angle 153.3°), excellent adsorption properties, and recyclability. Therefore, FCGA had a very promising application in circulating selective oil absorption.

Enhanced construction of 3D carbon skeleton through molten salt coupling activation effect for high efficiency capacitive deionization of lead (II) ions removal in wastewater

Efficiently eliminating of highly toxic ultra-dilute lead ions (Pb2+) from wastewater is a challenging task. Capacitive deionization (CDI) technology, based on the electrochemical capacitance mechanism, has emerged as a pivotal approach to address this challenge. In this work, a KNO3-mediated molten salt-coupled activation strategy was proposed to prepare nitrogen-doped hierarchical porous biomass carbon electrode material (3DCF-650-0.2) with a three-dimensional carbon skeleton, which was integrated into a symmetrical CDI device for Pb2+ removal. The 3DCF-650-0.2 electrode exhibited a high specific capacitance of 330.3 F g-1 at a current density of 1 A g-1, with a capacity retention rate of 98.45% after 10,000 cycles at 10 A g-1. Furthermore, the electrochemical adsorption capacity of the CDI device for Pb2+ reached 72.86 mg g-1 (1.2 V, 50 mg L-1), and the CDI device retained a high adsorption capacity of 91.14% after twenty adsorption/desorption cycles. These excellent adsorption properties are attributed to the in-situ activation and gas foaming of KNO3, which favors the production of reasonable pore structure (electric double-layer capacitance) and an appropriate pyrrolic nitrogen doping amount (selective adsorption) in the carbon materials. This work provides insight into the mechanism of the molten salt-coupled activation strategy, offering new ideas for the targeted design of high-performance CDI biomass carbon materials.

Solid‐phase synthesis of silicalite‐1 molecular sieve based on fly ash and its CO2 adsorption performance

AbstractIn this work, an alkali melting‐pickling assisted solid phase synthesis method of S‐1 zeolite molecular sieve with excellent adsorption properties for CO2 was successfully developed by using solid waste fly ash. SiO2 with a purity of up to 97.84% was successfully extracted by using alkaline fusion activation, high temperature calcination and pickling. The CO2 adsorption capacity of the prepared SiO2 was 0.51 mmol/g at 298 K and 1 bar. Silicalite‐1 molecular sieve was prepared by solid phase synthesis method using SiO2 extracted from fly ash as silicon source. The results showed that the prepared Silicalite‐1 had good morphology and relatively high crystallinity. The specific surface area is 623.30 m2/g, and the total pore volume is 0.31 cm3/g. In addition, the adsorption capacity of CO2 was 2.05 mmol/g at 298 K and 1 bar. Compared with the prepared SiO2, the adsorption capacity of CO2 by Silicalite‐1 molecular sieve increased by four times. Moreover, under the test condition of 298 K, it has a high selectivity coefficient for CO2/N2 mixed gas, and after 10 times of adsorption‐desorption cycle tests, the adsorption capacity of Silicalite‐1 molecular sieve for CO2 does not change significantly, and its adsorption rate can still be as high as 89.31%. The results indicate that Silicalite‐1 molecular sieve prepared by solid phase synthesis method has good adsorption selectivity and adsorption–desorption cycle regeneration stability, and can be used in the field of CO2 adsorption, separation and purification. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.

Comparative study of silica-based porous materials in the purification of radioactive wastewater

A significant challenge in the treatment of low-level radioactive wastewater is the effective purification of low-concentration radionuclides. Silica-based adsorbents are advantageous for the deep-purification of low-concentration metal ions. This study investigates three primary types of silica-based adsorbents: functionalized mesoporous silica, various modified zeolites, and mesoporous calcium silicate hydrate (C-S-H). These adsorbents were synthesized and their deep-purification effects on heavy metals and radionuclides were compared. The results indicated that mesoporous silica showed relatively poor adsorption for most metal ions. Zeolites outperformed mesoporous silica, with Zn framework-modified zeolites showing enhanced adsorption for several metal ions. Notably, C-S-H displayed superior adsorption performance, achieving high adsorption capacities for various metal ions and radionuclides. Specifically, at a dose of 0.5 g/L, the adsorption efficiency of C-S-H for numerous radionuclides in nuclear power plant wastewater exceeded 92–99 %, highlighting its potential for practical applications. An in-depth analysis of the physical and chemical structure and the adsorption mechanisms of C-S-H revealed its large mesoporous structure and electrostatic attraction to cations across a wide pH range. Multivalent cations were removed through exchange with Ca2+ in C-S-H, whereas monovalent cations were removed through exchange with Na+ in C-S-H. The cyclic structure of silica-oxygen tetrahedra in C-S-H, which promotes large pore formation and provides abundant ion exchange sites, underpins its excellent adsorption properties. This study offers valuable insights for the selection and application of silica-based materials in radioactive wastewater treatment.

Preparation of porous carbon from hydrothermal treatment products of modified antibiotic mycelial residues and its use in CO2 capture

Antibiotic mycorrhizal residues (AMR) are valuable organic wastes but have become a significant environmental and economic challenge due to their potentially hazardous nature and high treatment costs. In this study, an environmentally friendly and low-cost in situ nitrogen-doped porous carbon material was successfully prepared by hydrothermal carbonisation combined with KOH activation for efficient CO2 capture. The obtained material was systematically characterized and tested, and its physical and chemical properties were analyzed. By adjusting the activation temperature from 600 to 800 °C, the prepared porous carbon materials exhibited different specific surface areas (648.41–1712.72 m²/g), pore volumes (0.310–0.879 cm³/g), and the nitrogen was uniformly distributed in the carbon skeleton. The optimal N-doped porous carbon demonstrated the adsorption capacities of 3.99 mmol g−1 at 25 ℃ and 5.35 mmol g−1 at 0 ℃ under 1 bar. In addition, the prepared adsorbents exhibited excellent CO2/N2 selectivity, high isosteric heat, and good cyclic stability. These excellent CO2 adsorption properties were attributed to the highly developed microporous structure of the materials and the uniformly distributed nitrogen functional groups in the carbon skeleton. Overall, the results highlight the great potential of this class of heteroatom-doped novel carbon materials as selective CO2 adsorbents, providing a practical way to seek efficient CO2 abatement solutions.

Elaboration of fibrous structured activated carbon from olive pomace via chemical activation and low-temperature pyrolysis

The objective of this study is to examine the preparation of activated carbon with a fibrous structure obtained from olive pomace through a chemical activation process using phosphoric acid (H3PO4) as the activating agent under air at a lower temperature. According to the findings, the most effective conditions to achieve high-performance activated carbon were 22 vol% of H3PO4, a 2-h chemical activation impregnation residence time at 50 °C, and a 500 °C pyrolysis temperature for 1 h. Structural analysis revealed that activated carbons possess highly developed textural and structural properties, resulting in an iodine value of 923 mg/g and a specific surface of 1400 m2/g. In addition to its microporosity, the produced carbon exhibits a highly developed fibrous structure, providing excellent adsorption properties. To confirm these results, SEM, FT-IR, XRF, XRD, Raman, and TGA techniques were employed. The fibrous carbon produced will expand the use of renewable carbon materials for removing various types of contaminants, including organic and inorganic pollutants in water, and numerous other industrial applications.

Mesoporous carbon nanospheres doped with rich non-metallic and metallic catalytic active sites: A high-performance electrochemical platform for sensing of chloramphenicol in food samples

The development of a low-cost, accurate sensing strategy for trace levels of chloramphenicol (CAP) residues in food is crucial but remains challenging. In this study, a high-performance electrochemical platform was developed to detect CAP in animal-derived foods using Ni2P embedded N, P-co-doped mesoporous carbon nanospheres (Ni2P@N,P-MCS). The Ni2P@N,P-MCS material, with a unique mesoporous structure and large specific surface area, exhibited excellent adsorption properties. The N, P-co-doped heteroatoms enhanced the electric conductivity and active centers of MCS, facilitating fast mass transport and electron transfer. The introduction of Ni2P increased the active sites and enhanced the electrocatalytic activity. Leveraging these advantages, the electrochemical sensor based on Ni2P@N,P-MCS demonstrated outstanding detection performance with a wide linear range from 0.04 to 250 μM and a low limit of detection of 12 nM. The sensor also showed good reproducibility, stability, and anti-interference properties. Furthermore, the sensor was successfully tested in milk and pork samples, showing satisfactory recovery rates and indicating its feasibility for real sample analysis.

High-effective, convenient and environmental-friendly MOFs-chitosan-glyoxal composite film for ceftizoxime adsorption: Behavior and mechanisms.

In this work, a novel PCN-222-chitosan-glyoxal (PCN@CSG2) composite film was constructed by loading PCN-222 in chitosan substrate, and used for ceftizoxime adsorption. The results demonstrated that the PCN@CSG not only had excellent adsorption properties for ceftizoxime, but also maintained excellent structural properties in harsh environments (strong acids and alkalis), making it have good recycling performance. Specifically, the adsorption kinetics and isotherms investigation demonstrated that the adsorption process followed the pseudo-second-order kinetic model and Freundlich isotherm model respectively, indicating that it was a multilayer process mainly controlled by chemisorption. The PCN@CSG possesses excellent absorptive capacity of 561.7 mg·g-1 and reaches equilibrium rapidly within 60 min, which is attributed to the structural advantages of PCN-222 and chitosan. The amino, carboxyl and hydroxyl functional groups of PCN-222 provide numbers of active sites and cationic chitin greatly promoted the electrostatic adsorption with negative ceftizoxime. In addition, the PCN@CSG has the advantages of renewable and environment-friendly for the biodegradation of chitosan. After five consecutive adsorption-desorption cycles, the removal rate was still higher than 90 %, confirming the excellent reusability of PCN@CSG. This work provided a great prospect for the design and application of shaped-MOFs composite materials for the removal of cephalosporins in environmental water.

Controlled synthesis of NiCoS@Fe6(OH)12(CO3) as efficient electrocatalyst for oxidation reaction in seawater and urea

In today's world, the efficient preparation of clean energy has become a problem for every country. Hydrogen is a very clean and easy to prepare energy source. In this paper, a hybrid materials of (Fe6(OH)12(CO3)) and sulphide (Ni9S8/Co9S8) was demonstrated as a catalytic electrode for efficient oxidation reaction in seawater and urea. The catalysts were prepared by a three-step hydrothermal-sulfuration-hydrothermal reaction, and the layered composites of hydroxides and sulfides were co-grown into nano-arrays, which exposed more reaction centers and shortened the electron transfer path. The three metal cations were also able to demonstrate different corrosion resistance and excellent adsorption properties for different environments, allowing the catalyst to present better electrochemical activity in seawater as well as in urea solution. In the oxidation reaction in urea solution (1 M KOH+0.5 M urea), the required voltage was only 1.33 V at a current intensity of 50 mA/cm2, and in the water oxidation reaction in seawater, the required voltage was only 1.47 V at a current intensity of 50 mA/cm2 for Ni9S8@Co9S8@Fe6(OH)12(CO3). Unfortunately, the durability of the catalyst need to be improved, the current density dropped from 40 mA/cm2 to 35 mA/cm2 and then remained for 12 h. Meanwhile, the comparison of electrochemical performance tests was performed before and after the IT test, it can be clearly seen that the overall performance of Ni9S8@Co9S8@Fe6(OH)12(CO3) decreased after the stability test, which may be related to the shedding of active species from the surface of the catalyst. As you can see through density functional theory (DFT) that Ni9S8 can promote the adsorption energy of urea and Co9S8 lowers the barrier to electron conduction. Many conjectures were made and confirmed in this study, and finally, it is hoped that seawater as well as industrial wastewater can be better utilized for the production of clean energy.

Brazilian bentonite/MgO composites for adsorption of cationic and anionic dyes.

Industrial effluents, especially those containing dyes, have become the main cause of contamination of water resources. In this context, Brazilian bentonite/MgO composites, with excellent adsorptive properties, were prepared and investigated for their effectiveness in removing cationic and anionic dyes from aqueous solutions. The new adsorbents were obtained using Brazilian bentonites and MgO using the mechanochemical method followed by heat treatment (at 700°C for 4h). Different characterization techniques were used for the chemical, mineralogical, thermal, surface, and morphological analysis of the raw clays and the composites. The experimental adsorption isotherms were quantified under different conditions of initial concentration, contact time, pH, adsorbent dosage, and temperature variation to interpret the adsorption mechanism of the crystal violet (CV) and Congo red (CR) dyes. The modeling results were obtained from the empirical Sips equation and Pseudo Second Order (PSO) kinetics, indicating that the adsorption of molecules is a heterogeneous phenomenon that occurs in a monolayer on the surface (ns > 1), with the adsorption rate determined by chemisorption. The composites showed the best removal efficiency performance compared to the raw bentonites, with an increase of 12% for the CV dye and 46% for the CR dye. In addition, the qmax values obtained were 423.02mg/g and 479.86mg/g (AM01). This research underscores the potential of Brazilian bentonite/MgO composites as a promising solution for the removal of cationic and anionic dyes from water, offering hope for future applications in the field of environmental engineering and materials science.

Preparation and characterization of biochar from four different solid wastes and its ampicillin adsorption performance.

The integration of biochar (BC) production from organic waste with ampicillin (AMP), an emerging pollutant, adsorption is a novel and promising treatment approach. In this study, peanut shells, coffee grounds, digestates, and oyster shells were used for BC production. Among these, the use of anaerobic digestate from food waste fermentation to produce extracts for antibiotic adsorption is relatively unexplored. The pyrolysis temperature was determined using thermogravimetric analysis (TGA) and the materials were characterized with BET, SEM, FTIR, and XRD. The TGA results indicate that PSB, CRB, and DSB underwent pyrolysis involving cellulose, hemicellulose, and lignin, whereas OSB underwent crystal formation. Characterization revealed that DSB has more functional groups, a superior mesoporous structure, appropriate O/C ratio, and trace amounts of calcite crystals, which are favorable for AMP adsorption. Adsorption experiments demonstrate that all four materials adhere to the Freundlich and Langmuir isotherm and Elovich kinetic models, indicating predominant physical adsorption, with some chemical adsorption also present. Thermodynamic studies demonstrate that BC is spontaneous during adsorption and is a heat-absorbing reaction. DSB exhibits the strongest AMP adsorption. A 53.81mgg-1 adsorbance was obtained at a dosage of 150mg, pH = 2, and 60°C. This study introduces innovative approaches for managing waste types and provides data to support the selection of suitable solid wastes for the preparation of BC with excellent adsorption properties. Furthermore, it lays the groundwork for future studies aimed at enhancing the AMP treatment efficacy.

Enrichment of deoxynojirimycin in mulberry using cation exchange resin: Adsorption/desorption characteristics and process optimization

Deoxynojirimycin (DNJ) is an α-glucosidase inhibitor with high food values. However, the complex and costly enrichment processes have greatly prevented its application. Herein, this study aimed to propose a simple and efficient enrichment process for DNJ from Morus alba L. extracts using cation exchange resins. The LSI and D113 resins were chosen due to their excellent adsorption and desorption properties. The adsorption characteristics agreed with the pseudo-first-order kinetic model and the Langmuir isotherm model. This adsorption was chemisorption, spontaneous, endothermic and entropy-driven. Furthermore, the concentration and pH of the extracts, desorption solvent, breakthrough and elution curves, sample loading and elution rate were investigated to optimize the enrichment process by resin column chromatography. The results also showed that the purity of DNJ was improved to 44.00 % with a total recovery of 78.21 % using the LSI-D113 combination strategy. This research demonstrated the industrial feasibility of DNJ enrichment using cation exchange resins.

The Phosphonitrilic-derived graphynes as promising adsorbents of greenhouse gases

The new hybrid graphyne-like materials with highly developed specific surface area and excellent greenhouse gas adsorption properties have been described. Inorganic P3N3Cl6 was selected as a building block and 1,4-diacetylene benzene was chosen as a linker for these materials. The chemical structure of P3N3Cl6 allows for creation of three-dimensional materials with the BET surface area ranging from 600 to 1000 m2 g−1 and a pore volume as high as 0.3 cm3 g−1. The obtained materials showed microporous structure and distinctive greenhouse gas adsorption properties. For those materials, CO2 adsorption reached as high as 1.5 mmol g−1, while for N2O ranged from 1.5 to 1.7 mmol g−1, and for CH4 was 0.4 mmol g−1 when adsorption was carried out at 100 kPa and 300 K. Moreover, obtained by the modified Dubinin adsorption model, the maximum adsorption values were 2.5–11 mmol g−1 depending on the type of materials used. This finding suggests that new materials are promising high-pressure adsorbents of greenhouse gases.