Methylene Blue Adsorption Capacity Research Articles

Fixed-bed adsorption of methylene blue using granular NaX zeolite/attapulgite composite: efficiency, mechanism and reusability of saturated G-NaX/A

A novel granular NaX zeolite/attapulgite (G-NaX/A) composite was developed to address the challenges of high pressure drop in fixed beds with powder synthetic zeolite and low adsorption capacity of natural zeolite. The synthesized G-NaX/A retains the micropores of NaX and the mesoporous of attapulgite. The BET specific surface area reached 481.17 m2/g, and the total pore volume was 0.3549 cm3/g. The G-NaX/A maximum methylene blue (MB) adsorption capacity was 1.56 times that of commercial granular activated carbon (7.41 mg/g). The breakthrough time and adsorption capacity improved with lower influent flow rate and MB concentration and higher pH. Under optimal conditions (flow rate: 150 mL/min, MB concentration: 25 mg/L, pH = 8), it achieved a maximum adsorption capacity of 11.51 mg/g and a breakthrough time of 2.54 h. The adsorption behavior of G-NaX/A was well-fitted by the Yoon–Nelson and Thomas models at different operating conditions. The mechanism studies revealed that MB (cation: C16H18SN3+) removal by G-NaX/A occurred through electrostatic attraction, ion exchange with Na+/Mg2+, surface coordination with ≡Al/SiOH, and surface physical adsorption. The regeneration studies confirmed the reusability potential of G-NaX/A by calcining at 500 °C for 2 h, and significantly improved adsorption capacity reaching about 14.39 mg/g, 16.31 mg/g and 14.07 mg/g across the three adsorption-regeneration cycles respectively. The findings support G-NaX/A technical feasibility, high adsorption capacity and potential for further scaling in fixed bed adsorption studies.

Polydopamine coating for enhanced electrostatic adsorption of methylene blue by multiwalled carbon nanotubes in alkaline environments

The removal of dye molecules in alkaline environments is an issue that should receive increased attention. In this study, the interaction mechanism between polydopamine-modified multiwalled carbon nanotubes (P-MWCNTs) and multiwalled carbon nanotubes (MWCNTs) with the cationic dye methylene blue (MB) in alkaline environments was explained in depth by adsorption, spectroscopy, and density functional theory (DFT). The mechanism of action and dominant forces between the adsorbent and adsorbate were analyzed graphically by introducing energy decomposition analysis (EDA) and an independent gradient model (IGM) into the DFT calculations. In addition, the force distribution was investigated through an isosurface. Moreover, batch adsorption studies were conducted to evaluate the performance of MWCNTs and P-MWCNTs for MB removal in alkaline environments. The maximum MB adsorption capacities of the MWCNTs and P-MWCNTs in solution were 113.3 mg‧g−1 and 230.4 mg‧g−1, respectively, at pH 9. The IGM and EDA showed that the better adsorption capacity of the P-MWCNTs originated from the enhancement of the electrostatic effect by the proton dissociation of polydopamine. Moreover, the adsorption of MB by MWCNTs and P-MWCNTs in alkaline environments was governed by dispersion and electrostatic effects, respectively. Through this study, it is hoped that progress will be made in the use of DFT to explore the mechanism of adsorbent-adsorbate interactions.

Studying the kinetics and removal mechanism of the methylene blue dye in a continuous adsorption process using prepared mesoporous materials

ABSTRACT This study investigated the removal of a typical organic pollutant methylene blue (MB) dye from wastewater by a prepared mesoporous SBA-15 adsorbent in a continuous adsorption system (fixed-bed column). The structural and textural properties of the SBA-15 adsorbent were determined using different characterization techniques. The adsorption of continuous system experiments assessed the bed height effect, initial concentration, and flow rate on a breakthrough curve. The kinetic constants and breakthrough curves were obtained using the Thomas and Yan models. The breakthrough results revealed that SBA-15 has an excellent adsorption efficiency for use in the continuous adsorption system. The findings explain that MB removal achieved the maximum uptake (84 mg/g) at 6 cm of bed height, 0.5 mL/min of flow rate, and 30 mg/L initial concentration of MB. SBA-15 can be efficiently regenerated by calcination and re-employed 5 times in a fixed-bed system without a significant loss in its adsorption capacity of MB from MB solutions. As a result, SBA-15 was determined as the appropriate media to be adsorbent for MB. This study suggests that the prepared SBA-15 is feasible to use effectively for MB removal from the wastewater.

The feedstock anatomical properties determine biochar adsorption capacities: A study using woody bamboos (Bambuseae) and methylene blue as a model molecule

Feedstock characteristics impact biochar physicochemical properties, and reproducible biochar properties are essential for any potential application. However, in most articles, feedstock aspects (i.e., taxonomic name of the species, part of the plant, and phenological phase) are scarcely reported. This research aimed at studying the effect of species and phenological stage of feedstock on the properties of the derived biochars and, thus, adsorption capacities in water treatment. In this study, we analysed the anatomical characteristics of three different woody bamboo species [Guadua chacoensis (GC), Phyllostachys aurea (PA), and Bambusa tuldoides (BT)] in culms harvested at two different phenological phases (young and mature), and statistically correlated them with the characteristics of the six derived biochars, including their adsorption performance in aqueous media. Sclerenchyma fibres and parenchyma cells diameter and cell-wall width significantly differed among species. Additionally, sclerenchyma fibres and parenchyma cell-wall width as well as sclerenchyma fibres cell diameter are dependent on the phenological phase of the culms.Consequently, differences in biochar characteristics (i.e., yield and average pore diameter) were also observed, leading to differential methylene blue (MB) adsorption capacities between individuals at different phenological phases. MB adsorption capacities were higher for biochar produced from young culms compared to those obtained from matures ones (i.e., GC: 628.66 vs. 507.79; BT: 537.45 vs. 477.53; PA: 477.52 vs. 462.82 mg/g), which had smaller cell wall widths and thus gave a lower percentage of biochar yield. The feedstock anatomical properties determined biochar characteristics and thus modulated adsorption capacities.

Facile Fabrication of Hydroxyapatite and Bentonite Encapsulated Biopolymeric Hybrid Composites for Selective Removal of Methylene Blue

AbstractDyeing industries release their hazardous dyeing effluents into the environment which affects the human health and ecosystem. Hence, the removal of dye from waste‐water is mandatory one. In this present study, focus on the fabrication of bio‐clay‐ceramic hybrid composites by dispersing bentonite (BT) clay and ceramic hydroxyapatite (HA) into alginate (Alg) and gelatin (Gel) polymeric matrixes by in‐situ method which gives BTHAAlg and BTHAGel hybrid composites for methylene blue (MB) removal. The various adsorption influencing parameters such as shaking time, adsorbent dosage, pH and initial MB concentration were optimized under batch method. The highest MB adsorption capacities of BTHAAlg and BTHAGel composites were found to be 43.70 and 47.50 mg/g respectively with optimized conditions of 100 mg/L of initial MB concentration, 40 min shaking time and 0.1 g dosages. In pH studies, the high MB adsorption capacity of bio‐clay‐ceramic composites were noticed at pH 11. The characterization techniques like FTIR, SEM and EDAX analysis were performed to find the physico‐chemical properties of bio‐clay‐ceramic composites. The equilibrium data of hybrid composites towards MB adsorption was well fitted with Langmuir isotherm model than D‐R and Fruendlich models because of higher r and low sd values. The negative values of ▵Go at three different temperatures (303, 313 and 323 K) indicate that the spontaneous nature of MB adsorption, while positive values of ΔHo and ΔSo revealed that the MB adsorption onto hybrid composites was endothermic in nature and more randomness occurred at solid/liquid interfaces. In kinetic studies, the MB adsorption onto hybrid composites was well fitted with pseudo‐second‐order and intra‐particle diffusion models. The electrostatic attraction and hydrogen bonding plays a dominant role in MB adsorption onto BTHAAlg and BTHAGel bio‐clay‐ceramic composites. The regeneration studies proposed that the hybrid composites can be reusable upto five cycles. Hence, the developed bio‐clay‐ceramic hybrid composites were act as best adsorbents for MB removal.

Surface enriched ternary hybrid via interfacial polymerization as an effective adsorbent for dye removal

Methylene blue (MB) is a carcinogenic pollutant that can negatively affect both human health and marine life. Developing effective adsorbents for MB removal is therefore crucial for ensuring safe human life and mitigating environmental issues. Herein, we present an interfacial polymerization to synthesize polydopamine assisted multi-walled carbon nanotubes stitched graphene oxide (PDA@MWNTs/GO) as an effective adsorbent for MB removal. Stitching the PDA layer interfacially onto MWNTs/GO effectively prevents disintegration, diminishes agglomeration/restacking issues, and maximizes adsorption sites. The inherent catecholamine functionality within the PDA layer significantly enhances hydrophilicity. These distinctive characteristics endowed the PDA@MWNTs/GO composite with exceptional adsorption capacity for the cationic MB. The effects of MB concentration, pH, and temperature on the dye solution were thoroughly investigated. The results of the adsorption isotherm and kinetics analysis revealed conformity with the Langmuir isotherm model and adherence to the pseudo-second-order kinetic model. Moreover, PDA@MWNTs/GO demonstrated removal efficiency, exceeding 90% after three consecutive cycles of reuse. The adsorption mechanism was driven by electrostatic attraction and π–π stacking. The superior adsorption performance, attributable to the diverse functionalities and high removal efficiency, demonstrates the potential of PDA@MWNTs/GO as an efficient adsorbent for MB and can also function for other cationic dye impurities.

Two‐Dimensional Copper‐Based Metal‐Organic Framework for Efficient Removal of Methylene Blue from Wastewater

Metal‐organic frameworks (MOFs) can effectively remove methylene blue (MB) from wastewater due to their abundant adsorption sites and multi‐level pores. In this paper, a copper‐based MOF: {[Cu·(L)·(H2O)]·(DMF)}n (1) (H2L = 2‐hydroxyterephthalic acid; DMF = N,N‐dimethylformamide), was synthesized by hydrothermal synthesis method. X‐ray single crystal diffraction showed that a two‐dimensional structure was formed by the carboxyl group of L2‐ in 1 took μ2‐η1：η1 bridged two adjacent Cu(II). In this two‐dimensional structure, the coordinated water molecules and hydroxyl group on L2‐ were distributed on the surface of 1. Thus, it had abundant adsorption sites. The transmission electron microscopy (TEM) of copper‐based MOF nano adsorbent showed that the particle diameter of the nano adsorbent prepared by a cell fragmentation apparatus was about 50 nm. The performance of the copper‐based MOF nano adsorbent in adsorbing MB indicated that the optimal adsorbent dosage was 0.20 g/L and the solution pH was 6. Under the optimal experimental conditions, its maximum adsorption capacity for MB was 143.3 mg/g, which was superior to most MOFs adsorbents. The adsorption thermodynamic analysis showed that the copper‐based MOF nano adsorbent at 25 ‐ 45 ℃ was an exothermic (△H < 0) , and spontaneous (△G < 0) process.

Zeolite supported zinc oxide nanoparticles composite: Synthesis, characterization, and photocatalytic activity for methylene blue dye degradation

In the first stage of this study, zinc oxide nanoparticles (ZnO-NPs) were synthesized. The synthesized nanoparticles were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), selected area diffraction (SAED), and X-ray diffraction analyses (XRD). Subsequently, a composite material was obtained by coating ZnO-NPs with zeolite from Rátka, Hungary. The photocatalytic degradation of ZnO-NPs using Hungarian zeolite in the ZnO-Zeolite composite was investigated. The objective was to evaluate the efficacy of the ZnO-Zeolite composite in degrading methylene blue (MB) under ultraviolet-visible spectroscopy (UV). It was observed that the composite materials were influenced by the light source. The degradation rates showed that the ZnO-Zeolite composite with 100 mg L−1 MB achieved the highest photodegradation rate of 96.70 % when exposed to sunlight for 210 min. These findings indicate that the ZnO-Zeolite composite with a 1:5 ratio has the potential to significantly increase the photocatalytic activity, achieving a high yield of 96.70 % compared to raw zeolite. In the last stage of the study, equilibrium, kinetic, and thermodynamic studies were carried out. The photocatalytic maximum adsorption capacity of MB for the ZnO-Zeolite composite was calculated as qm= 41.32 mg g−1. In the adsorption and kinetic studies of the obtained composite, the best results were obtained with the Langmuir adsorption isotherm and pseudo-second-order kinetics. A desorption study has been conducted, and it has been determined that the composite can be reused for up to 7 cycles.

Repurposing cottonseed meal as dye biosorbent

We successfully repurposed cottonseed meal (CSM) into alginate composite hydrogel beads for dye adsorption via a simple and efficient method. The beads entrapped CSM with up to 80 wt%. Effect of CSM on the physiochemical properties of composite hydrogel beads including swelling behaviors, chemical structures, thermal stability, and methylene blue (MB) adsorption capacity, was investigated. Compared to alginate gel beads, the alginate/CSM composite system exhibited a drastic increase in thermal stability and a synergistic effect in dye adsorption capacity, where the dye adsorption capacity was well maintained, despite the inherently lower capacity when used alone. Such synergistic effect appeared to be linked to the reduced size of CSM particles within the gel network, while dye adsorption mechanism was attributed to the electrostatic attraction and hydrogen bonding between the biosorbents and dye. Our current study offers a feasible and cost-effective approach for upcycling CSM as biosorbent for dye decontamination.

Furfuryl-pyridinium-functionalization of flaxseed gum for effective methylene blue removal from aqueous solution

This study describes the modification of flaxseed gum (FSG) via furfural to obtain a furfuryl-pyridinium modified adsorbent (Flax-Py) with improved adsorption characteristics towards methylene blue (MB) versus results obtained for unmodified FSG. Materials characterization was achieved via complementary spectral methods (NMR, XPS, FT-IR, Raman, and XRD) as well as thermogravimetric analysis (TGA) and ζ-potential measurements. Synthetic modification of FSG to yield Flax-Py that led to enriched N-content (2.75 atom-% versus 0.76 atom-% for FSG), and the conversion of furfuryl to pyridinium was incomplete (ca. 50 %), where both moieties were identified. The adsorption isotherms at pH 7 showed that FSG possessed favorably high MB adsorption capacity (ca. 540 mg/g); while Flax-Py was notably lower (167 mg/g). Flax-Py facilitated 100% MB removal at low dye concentrations (1-10 mg/L) versus 50 % MB removal for the FSG bioadsorbent. Further, Flax-Py showed moderate loss of adsorption with MB (ca. 12-16% dye removal) after five regeneration cycles. Flax-Py revealed improved settling characteristics (time, density, gelation, and solubility) that facilitate enhanced phase separation of FSG fractions by circumventing the need for centrifugation. The adsorption mechanism was attributed primarily to H-bonding effects with secondary contributions due to electrostatic interactions (negative ζ-potential above pH 4.2). This study successfully modified FSG to obtain an improved adsorbent (Flax-Py) attaining nearly quantitative MB dye removal at environmentally relevant concentrations (< 15 mg/L).

KMnO4 modified magnetic hydrochar for efficient adsorption of malachite green and methylene blue from the aquatic environment

This study exploited magnetic citrus peel hydrochar (MHC) modified by KMnO4 (MHC/Mn) for the removal of methylene blue (MB) and malachite green (MG). Effects of initial concentration, pH, dosage, temperature, and ion strength on MHC/Mn adsorption properties were investigated. The adsorption kinetics, isotherm, and mechanism were further explored. The results indicated that Fe3O4 was successfully embedded and MnO2 was coated on MHC after modification. The experiment data were well fitted to the pseudo-second-order kinetic model and Langmuir isotherm model. Thermodynamic parameters showed that the adsorption of MHC/Mn to MB is spontaneous and endothermic, and the adsorption of MG is spontaneous and exothermic. The mechanism of MB and MG interaction with MHC/Mn includes electrostatic interaction, hydrogen bond, surface complexation, and π-π interaction. The maximum adsorption capacity of MB and MG calculated were 175.63 mg/g and 1402.17 mg/g. After four adsorption–desorption cycles, the removal rate of MB and MG were 85.11 % and 69.29 %. MHC/Mn is an economical and environmentally favorable adsorbent for the removal of MB and MG in wastewater.

Hydrothermal carbonization of biomass waste and application of produced hydrochar in organic pollutants removal

This novel research, presents the study of utilizing the wild almond shell as biomass waste to fabricate hydrochar using the hydrothermal carbonization (HTC) method based on a central composite design (CCD) with two independent variables (time and temperature) and three responses; productivity, higher heating value (HHV) and norfloxacin (NOR) adsorption capacity. The prepared hydrochar at 200 °C and 8 h was then employed to produce activated carbon (AC) by chemical-thermal activation technique. Hydrochar and AC were characterized using XRD, BET, SEM-EDX, Raman, and FTIR techniques. The pore development, resulting in a rise in the SBET (637.46 m2/g) value occurred after the activation process. Moreover, the results of XRD and Raman analyses revealed a decrease in graphitization degree. The adsorption of norfloxacin, methylene blue (MB), and sunset yellow (SY) by prepared hydrochar and AC were studied to assess the impact of the pH of the solution, initial concentration, temperature, and contact time. The maximum adsorption capacity for NOR, MB, and SY using hydrochar and AC were 85.37, 153.46, 93.35, and 384.1625, 556.465, 264.93 mg/g, respectively. The experimental data for the adsorption of NOR, MB, and SY using hydrochar and AC illustrated a good fit with the PSO model. Besides, the Langmuir and Freundlich models indicated better fitting with empirical data obtained for the adsorption of NOR, MB, and SY, respectively. Thermodynamic study outcomes validated the exothermicity and spontaneity of the adsorption process for both absorbents. This study presents a new opportunity to develop the circular economy by fabrication of sustainable adsorbents with high adsorption capacity for organic pollutants from biomass waste.

Ultrasonic-Assisted Nitrate Anion Incorporation in Triaminoguanidium Chloride Based Covalent Organic Polymer for Methylene Blue Dye Adsorption.

Terephthalaldehyde-triaminoguanidium chloride covalent organic polymer, Te-TGCl COP can facilely be incorporated with NaNO3 by sonication. Te-TGCl COP incorporated with NaNO3 via ultrasonication adsorbs Methylene Blue (MB) dye. Te-TGCl COP alone shows negligible adsorption capacity for MB, however, when treated with NaNO3, its adsorption capacity emerges slightly. Moreover, ultrasonication of the NaNO3 treated COP, Te-TG-NaNO3 COP shows dramatic increase in its adsorption capacity for MB (qe for Te-TGCl COP ≈0 mg g-1; for Te-TG-NaNO3=17.65 mg g-1). Emergence of MB dye adsorption property in Te-TG-NaNO3 COP composite may be attributed primarily to the electrostatic interaction of MB dye molecules with nitrate anions and the sonochemical effect caused fibrous morphological structure of the adsorbent material. The kinetics of MB dye adsorption onto Te-TG-NaNO3 COP composite exhibits an excellent fit for the pseudo-second order model, suggesting the rate-determining step to be chemisorption. Homogeneous monolayer adsorption of MB dye onto Te-TG-NaNO3 COP composite can be suggested as the Langmuir isotherm model seemed to be fitted well.

Assessment of chromite ore wastes for methylene blue adsorption: Isotherm, kinetic, thermodynamic studies, ANN, and statistical physics modeling

This research investigates the adsorption potential of chrysotile and lizardite, two minerals derived from chromite ore wastes, for the uptake of Methylene Blue (MB) dye from waste streams. The characterization of these minerals involves XRD, XRF, FTIR, and SEM. Results confirm the dominance of polymorphic magnesium silicate minerals, specifically chrysotile and lizardite, in the samples. The FTIR spectra reveal characteristic vibration bands confirming the presence of these minerals. The SEM analysis depicts irregular surfaces with broken and bent edges, suggesting favorable morphologies for adsorption. N2 adsorption-desorption isotherms indicate mesoporous structures with Type IV pores in both adsorbents. The Central Composite Design approach is employed to optimize MB adsorption conditions, revealing the significance of contact time, adsorbent mass, and initial MB concentration. The proposed models exhibit high significance, with F-values and low p-values indicating the importance of the studied factors. Experimental validation confirms the accuracy of the models, and the optimum conditions for MB adsorption are determined. The influence of solution acidity on MB uptake is investigated, showing a significant enhancement at higher pH values. Isothermal studies indicate Langmuir and Freundlich models as suitable descriptions for MB adsorption onto chrysotile and lizardite. The maximum adsorption capacities of MB for chrysotile and lizardite were found to be 352.97 and 254.85, respectively. Kinetic studies reveal that the pseudo-first-order model best describes the adsorption process. Thermodynamic analysis suggests an exothermic and spontaneous process. Statistical physics models further elucidate the monolayer nature of adsorption. Additionally, an artificial neural network is developed, exhibiting high predictive capability during training and testing stages. The reusability of chrysotile and lizardite is demonstrated through multiple regeneration cycles, maintaining substantial adsorption potential. Therefore, this research provides comprehensive insights into the adsorption characteristics of chrysotile and lizardite, emphasizing their potential as effiective and reusable sorbents for MB uptake from wastewater.

Preparation of porosity-adjustable porous adsorbent materials derived from coal solid waste

Coal solid waste (CSW) was explored as precursor to prepare porous adsorption material (ACSW) by carbon dioxide activation. The effects of activation method (direct activation and pre-carbonization followed by activation), activation temperature, and activation time were systematically investigated. The burn-off characteristics of the CSW were measured, the ACSW were characterized by field emission scanning electron microscope, gas adsorption instrument and Raman spectrometer, and, in parallel, the adsorption ability was studied using methylene blue (MB) as a typical pollutant. The results showed that compared with direct activation, pre-carbonization reduced the carbon loss, increased the pore volume with pore size less than 1 nm, improved the carbon structural order and increased the MB adsorption performance. In addition, the evolution of the structure of the ACSW strongly depended on the activation temperature and time. With the increase of the activation time, the pore structure evolution underwent three stages: pore forming, expanding, and collapsing. Pore forming mainly involved clearing scattered graphite structures and amorphous carbon. Pore expanding mainly relies on consumption of regular graphite carbon crystal structure. At low temperature of 800 °C, micropores fully developed. As the activation temperature increased to 850–900 °C, pore expansion became apparent, mainly forming pores of 1–5 nm. Moreover, the MB adsorption capacity was positively correlated with the pore volume with pore size less than 5 nm. The burn-off can serve as an indicator for evaluating pore structure and the adsorption performance and when it was ∼25.5 %, the ACSW had the largest pore volume with pore size less than 5 nm and the highest MB adsorption capacity.

Magnetic, Biocompatible and Biodegradable Carboxymethyl Cellulose‐Based Hydrogel for Cationic Dye Adsorption

AbstractEnsuring the availability of water resources that are both clean and safe is crucial for the preservation of environmental health and the well‐being of humans. Here, we fabricated carboxymethyl cellulose‐based hydrogel nanocomposite using acrylic acid (AA) and 2‐acrylamido‐2‐methylpropane sulfuric acid (AMPS) monomers and Fe3O4 nanoparticles through a free radical crosslinking process for adsorption of dyes from contaminated water. The synthesized nanocomposite hydrogel was characterized using various techniques, including TEM, XRD, FTIR, SEM‐EDS, TGA, and AFM analysis. The swelling capacity of samples in an aqueous medium at multiple pH levels and the presence of different salts were investigated. The adsorption efficiency of methylene blue (MB) and crystal violet (CV), emphasizing the effect of hydrogel concentration and the medium's pH, was studied. It was concluded that the hydrogel sample containing 17 % AMPS and 51 % AA had better swelling capacity and dye removal efficiency. The dye adsorption kinetics data were fitted to pseudo‐first and second‐order kinetic models and the Langmuir and Temkin isotherm models. The maximum adsorption capacity for MB and CV was 53.97 and 53.57 mg/g, respectively. It was revealed that the pseudo‐second‐order kinetic model could best describe adsorption (qe=79.2 mg/g for MB and qe=65.8 mg/g for CV). The intra‐particle diffusion model was found to be the rate‐limiting mechanism of dye adsorption. Thermodynamic studies proposed that the adsorption of MB and CV was spontaneous and endothermic. Additionally, magnetic nanocomposite hydrogel‘s reusability up to four successive cycles further determines its probability of adsorption of dyes from wastewater.

Green synthesis of metal nanoparticles from Codium macroalgae for wastewater pollutants removal by adsorption

AbstractAlgae have adsorption properties and reducing agents due to their rich content. In this study, palladium nanoparticles (Pd NP), platinum nanoparticles (Pt NP), and iron oxide nanoparticles (Fe3O4 NP) were prepared from Codium macroalgae using green synthesis. The structure of the synthesized nanoparticles was elucidated by X‐ray diffractometry, Fourier transforms infrared spectroscopy, Brunauer–Emmett–Teller analysis, transmission electron microscopy, ultraviolet‐visible spectroscopy and scanning electron microscopy‐energy dispersive X‐ray spectrometry and their use as nanoadsorbents for the removal of pollutants from aqueous media was investigated in detail. Naproxen (NPX), an anti‐inflammatory drug, and the dyes methylene blue (MB) and cresol red (CR) were selected as pollutants for this study. Batch adsorption experiments were conducted using both real wastewater obtained from the Organised Industrial Zone of Isparta Province and synthetic water samples prepared with tap water from Burdur Province and pure water. Under optimum adsorption conditions, Pd NP showed significant efficiency in the real wastewater sample, with an adsorption capacity of 37.19 and 50.03 mg g–1 for CR and NPX, respectively, within 150 min. In comparison, Pt NP showed an adsorption capacity of 40.01 mg g–1 for MB within the same timeframe. These findings indicate that while Pd NP showed the highest adsorption capacity for both CR and NPX, Pt NP showed the highest adsorption capacity for MB. The Langmuir model and the pseudo‐second‐order equation were more suitable to describe the adsorption behavior of CR, MB, and NPX. In addition, studies on the desorption and reusability of the nanoadsorbents were carried out under the same optimum experimental conditions.

Full utilization of poplar sawdust with chemical-mechanical pretreatment for coproduction of xylooligosaccharides, fermentable sugars and porous carbon materials

In recent decades, one of the major challenges of biorefinery is the full utilization of lignocellulosic components for coproduction of value-added materials. In this context, we proposed an integrated process of acetic acid (AC) pretreatment, Papir Forsknings Institutet (PFI) refining and enzymatic hydrolysis to coproduce xylooligosaccharides, fermentable sugars and lignin-based porous carbon materials. Results showed AC pretreatment (170 ºC, 60 min, 5 w/v % acetic acid and 5% 2-naphthol addition based on dry mass of biomass) resulted in maximum xylooligosaccharids (XOS) yield of 51.08%. The integrated process of AC pretreatment assisted by 2-naphthol-7-sulfonate addition and PFI post-refining led to cellulose hydrolysis yield of 98.20% and lignin-based porous carbon materials with methylene blue adsorption capacity of up to 749.17 mg/g. Moreover, it was found lignin repolymerization inhibitors (i.e. 2-naphthol, 2-naphthol-7-sulfonate) in acid pretreatment helped increase the specific surface area of substrate and decrease surface lignin coverage, which enhanced cellulose accessibility to cellulase enzymes. Moreover, they enhanced lignin detaching during enzymatic hydrolysis, which reduced cellulase aggregation and promoted the ease of cellulose hydrolysis. Results demonstrated an efficient pretreatment strategy to maximize coproduction of xylooligosaccharids, fermentable sugars and lignin materials from lignocellulosic biomass for full utilization.

Construction of 3D-Printed Sodium Alginate/Chitosan/Halloysite Nanotube Composites as Adsorbents of Methylene Blue.

In this study, sodium alginate/chitosan/halloysite nanotube composites were prepared by three-dimensional printing and characterized in terms of morphology, viscosity, thermal properties, and methylene blue (MB) adsorption performance. The high specific surface area and extensively microporous structure of these composites allowed for effective MB removal from wastewater; specifically, a removal efficiency of 80% was obtained after a 60 min treatment at an adsorbent loading of 1 g L-1 and an MB concentration of 80 mg L-1, while the maximum MB adsorption capacity equaled 376.3 mg g-1. Adsorption kinetics and isotherms were well described by quasi-second-order and Langmuir models, respectively. The composites largely retained their adsorption performance after five adsorption-desorption cycles and were concluded to hold great promise for MB removal from wastewater.

Removal of methylene blue using magnetic Na-bentonite composite in aqueous Solutions

The present work focuses on the development of a new magnetic composite material that would be practical and effective for the removal of methylene blue (MB) dye from water. This composite material was chemically prepared from bentonite and iron salts. It was characterized by ATR-FTIR, DRX, SEM and EDS. The adsorption study showed a relatively high adsorption capacity of MB on the composite (86.2 mg/g) and an MB removal efficiency of 100%. In a study of the influence of certain operating parameters, the effect of pH and temperature on MB removal efficiency was found to be negligible. However, the results of the kinetic and thermodynamic study showed that MB adsorption follows the pseudo-second- order and Langmuir model. Of the eluents tested, acetic acid proved to be the most efficient, with an MB desorption efficiency of 90%. The results obtained show that magnetic bentonite is an interesting solution for the removal of dyes in water by adsorption.