Methylene Blue Adsorption Capacity Research Articles

Optimization of activation by peroxidation and photo-assisted peroxidation of biochar produced from sewage sludge

Biochar from biomass, a cost-effective and sustainable alternative to pulverized activated carbon (PAC), often faces limitations in pore size and surface functionality. Hydrogen peroxide (H₂O₂) activation can enhance biochar's surface properties but requires large quantities and high concentrations, increasing production costs. Advanced oxidation methods, such as H₂O₂/UV radiation, can reduce H₂O₂ usage by generating highly reactive hydroxyl radicals (*OH). This study investigates biochar production from activated sewage biosolids using H2O2 activation and H2O2/UV radiation. Optimization was conducted via a central composite rotational design, varying activation parameters activation pH (1.5, 4.0, 7.0, 9.0, and 11.5) and H2O2 concentration (0, 10, 20, 30, and 40 vol), with methylene blue (MB) adsorption capacity as the metric. Characterization was performed using FTIR, SEM, EDS, XRD, and N2 adsorption/desorption techniques. Results indicated optimal biochar activation at pH 11.5 with 20 vol% H2O2. Activation pH was more significant than H2O2 concentration. Desirability curve analysis suggested that optimized parameters did not significantly enhance adsorption capacity, with desirability values at 93.053 %. Overall, H2O2 efficiently increased surface area by degrading the adsorbent, while H2O2/UV effectively removed impurities.

Effect of dissolution for black carbon on the adsorption capacity for methylene blue: Equilibrium, kinetics and thermodynamics

Black carbon was widely researched due to its significant role on the global carbon cycle and contaminant transport, and most people were concerned about the property of the dissolved black carbon from black carbon. In this work, we focused on the research of the residual those of black carbon. Two kinds of black carbon originated from peanut shell and bamboo were prepared and the corresponding residual black carbons were also obtained by the ultrasonic dissolution process. It was found the chemical and structure properties of residual black carbon changed a lot compared to black carbon. Using methylene blue as a target contaminant, the adsorption capacity of methylene blue by the residual black carbon was greater than that of black carbon. The adsorption capacity of black carbon-bamboo for methylene blue increased from 11.1 mg/g to 16 mg/g after the dissolution process, and the adsorption capacity of black carbon-peanut shell for methylene blue increased from 14 mg/g to 23 mg/g. The various influencing factors, such as the pH, initial concentration, temperature and adsorbent dosage, were systematically studied. The black carbons derived from peanut shell before and after the ultrasonic dissolution process both showed greater adsorption capacities for methylene blue. To further elucidate the methylene blue adsorption process, different kinds of isotherm and kinetics models were applied to simulate the experimental data. The results indicated that the Langmuir isotherm model was suitable to all the carbons before and after the ultrasonic dissolution process, and the pseudo-second-order model showed great simulation for the adsorption of methylene blue. In addition, the analysis of the thermodynamic study revealed that the adsorption processes of methylene blue were endothermic and spontaneous. Overall, results obtained from this work revealed the black carbon after been dissolved showed better adsorption capacity for contaminant.

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

AbstractMetal‐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 °C was an exothermic (ΔH<0), and spontaneous (ΔG<0) process.

Synergistic effect of adsorption and photolysis on methylene blue removal by magnetic biochar derived from lignocellulosic biomass

In this study, magnetic biochar was synthesized by doping Fe3O4 onto the biochar surface followed by analysis of its properties. The efficiency of methylene blue (MB) removal through the combined processes of adsorption and photolysis was assessed. The presence of Fe3O4 on the biochar surface was confirmed using Raman spectroscopy and X-ray photoelectron spectroscopy. The magnetic biochar, after MB adsorption, showed a magnetism of 39.50 emu/g leading to a 97.07 % recovery rate. The specific surface area of biochar was higher (380.68 m2/g) than that of magnetic biochar (234.46 m2/g), and the maximum adsorption capacity of MB was higher in the biochar (0.03 mg/g) than that in magnetic biochar (0.02 mg/g) under the optimal conditions for MB adsorption. The MB adsorption experiments using biochar or magnetic biochar were optimally conducted under 10–20 mg/L MB concentration, 1 g biochar dosage, pH 12, 200 rpm rotation speed, 25 °C temperature, and 30 min duration. Under dark conditions, biochar had a higher MB removal rate, at 83.91 %, compared to magnetic biochar, at 78.30 %. Under visible light (λ > 425 nm), magnetic biochar effectively removed MB within 10 min, highlighting the synergistic effect of adsorption and photolysis. MB is physically and chemically adsorbed by the monolayer on the surface of EB and EMB according to adsorption behavior.

Heteroatom doped biochar-aluminosilicate composite as a green alternative for the removal of hazardous dyes: Functional characterization and modeling studies

In this work, a novel nitrogen-doped biochar bentonite composite was synthesized by a single-pot co-pyrolysis method. Batch studies were conducted to evaluate the performance of the developed composite in eliminating synthetic dyes from the aqueous matrix. Energy dispersive X-ray spectroscopy analysis and field emission scanning electron microscopy imaging confirmed the N doping and bentonite impregnation into biochar. X-ray photoelectron spectroscopy analysis revealed that the N atoms were doped interstitially into the carbon matrix of biochar in the form of pyridinic and pyrrolic nitrogen. Simultaneous heteroatom doping and bentonite impregnation reduced the specific surface area to 41.721 m2 g−1 but improved the adsorption capacity of biochar for dye adsorption. Further experimental studies depicted that simultaneous bentonite impregnation and N doping into the biochar matrix is beneficial for direct blue-6 (DB-6) and methylene blue (MB) removal and maximum adsorption capacities of 53.17 mg. g−1 and 41.33 mg. g−1 were obtained for MB and DB-6, respectively, at varying conditions. Adsorption energetics of the dyes with the developed composite portrayed the spontaneity of the process through negative ΔG values. The Langmuir and Freundlich isotherm models fitted the best for MB and DB-6 adsorption. The monolayer adsorption capacity and favourability factor for MB and DB-6 adsorption were calculated to be 54.15 mg. g−1 and 0.217, respectively from the best-fitted isotherms. Based on density functional theory calculations and spectroscopic studies, major interactions governing the adsorption were predicted to be charge-based interactions, π-π interactions, H-bonding, and Lewis acid-base interactions.

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.

Synthesis and application of biochar from agricultural by-products. Effect of pyrolysis temperature on the acid-base properties of biochar

Biochar was synthesized from banana peels using the pyrolysis method in a nitrogen gas environment. The pyrolysis temperature ranged from 100°C to 500°C with a heating rate of 5°C per minute and a pyrolysis time of 1.5 hours. The influence of the pyrolysis temperature on the acid-base properties of the biochar surface was evaluated through characteristic SEM and BET measurements. Boehm titration showed a gradual decrease in the total acid functional groups and an increase in the total base functional groups with the increasing pyrolysis temperature. Methylene Blue (MB) was used as a model substance to investigate the adsorption properties of the synthesized biochar. The Langmuir and Freundlich models were employed to describe the adsorption equilibrium. The kinetics of MB adsorption followed a pseudo-second-order kinetic equation. The adsorption capacity of MB by biological charcoal was influenced by the acid-base properties of the material, indicating the impact of the pyrolysis temperature.

Enhanced photocatalytic regeneration of carboxymethyl cellulose/lignin/ZnO complex hydrogel after methylene blue adsorption

The biodegradable, nontoxic, and renewable carboxymethyl cellulose (CMC) hydrogel has been developed into a green adsorbent. However, the weak chemical interaction limits its adsorption capability and reusability. This work incorporated lignin with complex structure and ZnO nanoparticles with photocatalytic properties into CMC hydrogel beads to improve the removal of methylene blue (MB) through chemical interaction. Scanning electron microscopic images and Fourier-transform infrared spectra confirmed the compatibility between lignin and ZnO nanoparticles as well as the increment of active sites for dye removal. The MB adsorption on CMC hydrogel beads was more significantly affected by the temperate and initial concentration compared to contact time, pH, and adsorbent dosage. The MB adsorption capacity of CMC hydrogel was improved to 276.79 mg/g after incorporating lignin and ZnO nanoparticles. The adsorption followed the pseudo-second-order kinetic model and Langmuir isotherm model, indicating chemical adsorption. After 6 cycles, the adsorption capacity was reduced by about 15 %. The UV irradiation could recover and improve MB adsorption capacity of CMC hydrogel beads containing ZnO nanoparticles due to the introduction of reactive oxygen species.

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 the 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 fibre cell diameters 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 leading to a lower percentage of biochar yield. The feedstock anatomical properties determined biochar characteristics which 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.

Response surface and DFT protocols for improvement of the adsorption process of lignocellulosic-based biomass for the removal of basic dyes

Jatobá-do-cerrado fruit shells, archetypical of lignocellulosic-based biomass, were used as an adsorbent to remove crystal violet (CV) and methylene blue (MB) from water. The adsorbent was characterized using various techniques, and kinetic studies showed dye adsorption followed second-order kinetics. An experimental design investigated the effects of pH and temperature on removal efficiency, with a quadratic model fitting the data best. The results suggest pH influences MB's adsorption capacity more than temperature and at 25 °C and pH 8, MB had a desirability value of 0.89, with 95 % removal efficiency. For CV, temperature had a greater influence, with a desirability value of 0.874 at 25 °C and pH 10, and 95 % removal efficiency. Adsorption isotherm studies revealed maximum adsorption capacities of 123.0 mg·g−1 and 113.0 mg·g−1 for CV and MB, respectively. Experimental thermodynamic parameters indicated an endothermic and spontaneous process which it was supported by quantum chemistry calculations. The protocols developed confirmed the potential for adsorbing CV and MB dyes in water, achieving over 73.1 and 74.4 mg g−1 dyes 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.

Nanofiber films reinforced with biomass extracts and their high efficiency in adsorbing dyes

In this study, polyacrylonitrile (PAN) was used as precursor and calcium Lignesulfonate (CLS) as additive to prepare composite films by electrospinning technology for the adsorption of methylene blue (MB) and Congo red (CR) dyes. The composite films were characterized by Brunauer-Emmett-Taylor analysis, Fourier transform infrared spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy (EDS). The effects of pH value, temperature, concentration and reaction time on adsorption efficiency were investigated. When the content of CLS is 20 wt%, the composite membrane has excellent adsorption performance, and the maximum adsorption capacity of MB and CR are 48 and 23 mg/g.

Optimization of Fe/Ni, Fe/Cu bimetallic nanoparticle synthesis process utilizing concentrated Camellia sinensis extract solution and activity evaluation through methylene blue removal reaction

In this study, we introduce a synthesis process of bimetallic nanoparticles (BNPs) Fe/Ni and Fe/Cu utilizing concentrated Camellia sinenis extract that was optimized with a solvent ratio of ethanol/H2O 4/1 (v/v), a metal ratio of 5/1 (w/w), a total polyphenol content (TPC) in the solution of 12.5 g.l−1, pH = 3–4, 25 °C, and the reaction time ranging from 30 min to 50 min. The structural and morphological characteristics of the resulting materials were determined using several techniques, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive x-ray spectroscopy (EDX), x-ray diffraction (XRD), and x-ray photoelectron spectroscopy (XPS). The maximum removal efficiency of methylene blue (MB) by BNPs Fe/Ni and Fe/Cu materials was found to be 88.60% and 91.06%, respectively, at a concentration of MB = 25 mg.l−1 and 25 °C. According to the results of the kinetic modeling study, the adsorption process of MB on the two BNPs materials followed second-order kinetics, with the maximum adsorption capacities of MB on Fe/Ni and Fe/Cu BNPs being 26.94 mg.g−1and 28.00 mg.g−1, respectively.

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.