Phosphorylating Tannin in Urea System: A Simple Approach for Enhanced Methylene Blue Removal from Aqueous Media.

Tannin, after lignin, is one of the most abundant sources of natural aromatic biomolecules. It has been used and chemically modified during the past few decades to create novel biobased materials. This work intended to functionalize for the first time quebracho Tannin (T) through a simple phosphorylation process in a urea system. The phosphorylation of tannin was studied by Fourier transform infrared spectroscopy (FTIR), NMR, inductively coupled plasma optical emission spectroscopy (ICP-OES), and X-ray fluorescence spectrometry (XRF), while further characterization was performed by scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX) and thermogravimetric analysis (TGA) to investigate the morphology, composition, structure, and thermal degradation of the phosphorylated material. Results indicated the occurrence of phosphorylation, suggesting the insertion of phosphate-containing groups into the tannin structure, revealing a high content of phosphate for modified tannin (PT). This elevated phosphorus content serves as evidence for the successful incorporation of phosphate groups through the functionalization process. The corresponding PT and T were employed as adsorbents for methylene blue (MB) removal from aqueous solutions. The results revealed that the Langmuir isotherm model effectively represents the adsorption isotherms. Additionally, the pseudo-second-order model indicates that chemisorption predominantly controls the adsorption mechanism. This finding also supports the fact that the introduced phosphate groups via the phosphorylation process significantly contributed to the improved adsorption capacity. Under neutral pH conditions and at room temperature, the material achieved an impressive adsorption capacity of 339.26 mg·g-1 in about 2 h.

Carboxymethyl cellulose/activated carbon/hydroxyapatite composite adsorbent for remediation of methylene blue from water media.

In the present study, activated carbon (AC), activated carbon/hydroxyapatite (AC/HAp), and carboxymethyl cellulose/activated carbon/hydroxyapatite (CMC/AC/HAp) composite adsorbents were prepared to remediation of methylene blue (MB) from water media. The pyrolysis method used the Pine cone as a natural precursor to synthesize AC. FTIR, XRD, Raman, BET, TEM, and SEM-Dot mapping techniques were applied to characterize synthesized adsorbents. Experimental results demonstrated that the maximum removal efficiency of AC, AC/HAp, and CMC/AC/HAp adsorbents under optimum conditions of pH 8, adsorbent dose 1 g/L, contact time 60 min, initial concentration 10 mg/L, and temperature 25 °C was computed to be 98.75, 98.86, and 98.93 %, respectively. Kinetic and equilibrium data were well-fitted with pseudo-second-order and Langmuir models, respectively. The maximum monolayer adsorption capacity of AC, AC/HAp, and CMC/AC/HAp was determined to be 40, 44.248, and 43.86 mg/g, respectively. FTIR results showed that hydrogen bonding and electrostatic interactions are the main mechanisms of the adsorption process. Results of the thermodynamic study showed that the adsorption process is spontaneous and exothermic. Finally, AC, AC/HAp, and CMC/AC/HAp composite adsorbents can be used as promising adsorbents for the remediation of MB from wastewater.

Rapid eco-friendly selective dye removal using modified chitosan-based sponges: Synthesis, characterization, and application.

The ongoing challenge of water scarcity persists alongside a concerning rise in water pollution driven by population expansion and industrial development. As a result, urgent measures are imperative to address the pressing need for a clean and sustainable water supply. In this study, a sustainable and green approach was utilized to prepare four chitosan-based sponges from a chemically modified chitosan with different alkyl chains in aqueous medium and at room temperature. The resulting sponges displayed excellent stability in water with outstanding dye removal efficiency. The adsorption capacity was associated with the alkyl chain length incorporated to the polymer backbone. All sponges displayed a high adsorption capacity of methyl orange (MO) ranges between 238 and 380 mg g-1, while a low capacity were obtained for methylene blue (MB) and Rhodamine B (RB). Competitive adsorption experiments were conducted on binary and ternary mixtures to assess the selective removal of MO from a mixture of dyes in which the separation factor was found to be ranging between 1.6 and 32. The adsorption kinetics isotherms of all sponges followed the pseudo-second-order, and the Langmuir model was found to be more suitable than the Freundlich for the adsorption of MO on the sponges. The chitosan-based sponges showed stable performance, robustness and reusability over 5 adsorption-desorption cycles, indicating their great potential for water treatment applications.

In situ growth of HKUST-1 on electrospun polyacrylonitrile nanofibers/regenerated cellulose aerogel for efficient methylene blue adsorption.

Dyes, as organic pollutants, are causing increasingly severe environmental problems. Metal-organic frameworks (MOFs) are considered promising dye adsorbents; however, their application is limited due to their powder or solid particle forms and limited reusability. Therefore, this study proposes an innovative approach to develop a novel MOF-based composite aerogel, specifically a HKUST-1/polyacrylonitrile nanofibers/regenerated cellulose (HKUST-1/PANNs/RC) composite aerogel adsorbent, for the adsorption of pollutants in water. This adsorbent was successfully prepared using a simple method combining covalent crosslinking, quick freezing, freeze-drying, in-situ growth synthesis, and solvothermal techniques. The HKUST-1/PANNs/RC composite aerogel exhibits a significantly large specific surface area, which is approximately 64 times greater than that of PANNs/RC (10.45 m2·g-1), with a specific surface area of 669.9 m2·g-1. The PANNs serve as a support framework, imparting excellent mechanical properties to the composite aerogel, enhancing its overall stability and recoverability. Additionally, the composite aerogel contains numerous -COOH and -OH groups on its surface, providing strong acid resistance and facilitating interactions with pollutant molecules through electrostatic interactions, π-π conjugation, n-π* interactions, and hydrogen bonding, thereby promoting the adsorption process. Using methylene blue (MB) as a probe molecule, the study results demonstrate that the HKUST-1/PANNs/RC composite aerogel has an adsorption capacity of 522.01 mg·g-1 for MB (25 h), exhibiting excellent adsorption performance. This composite aerogel shows great potential for application in water pollution control.

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 modified of chitosan by TiO2@MWCNT nanohybrid for the efficient removal of organic dyes and antibiotics.

Considering the increase in the discharge of industrial effluents containing dyes and antibiotic resistance as a consequence of increasing the prescription and easy distribution of antibiotic drugs at the global level, designing efficient, biodegradable and non-toxic absorbents is necessary to reduce environmental harm effects. Herein, we present a series of novel eco-friendly ternary hybrid nanocomposite hydrogels CS/TiO2@MWCNT (CTM) composed of chitosan (CS), TiO2, and multiwalled carbon nanotube (MWCNT) for removal of methylene blue (MB) and methyl orange (MO) and common antibiotic ciprofloxacin (CIP) in aqueous medium. The combination of MWCNT and TiO2 improves the physicochemical properties of CS hydrogel and increases the adsorption capacity toward pollutants in the presence of different loadings. CTM hydrogel showed a specific surface area of 236.45 m2 g-1 with a pore diameter of 7.89 nm. Adsorption mechanisms were investigated in detail using kinetic, isotherm, and thermodynamic studies of adsorption as well as various spectroscopic techniques. Adsorption of these pollutants by CTM nanocomposite hydrogel occurred using various interactions at different pHs, which showed the obvious dependence of CTM adsorption capacity on pH. Electrostatic attractions, complex formation, π-π stacking and hydrogen bonds played a key role in the adsorption process. The adsorption of MB, MO, and CIP was fitted with the Langmuir isotherm with maximum adsorption capacities of 531.91, 1763.6, and 1510.5 mg g-1, respectively. CTM had a minor decrease in adsorption strength and showed good structural stability even after 8 adsorptions-desorption cycles. The total cost of producing a 1 kg adsorbent was calculated to be $ 450, which helped us determine the economic feasibility of the adsorbent in large-scale applications.

Selective adsorption of anionic dyes by a macropore magnetic lignin-chitosan adsorbent.

Dyes pollution is well known for their hazardous impacts on human health and the environment. The removal of dyes from wastewater has become an important issue. In this study, magnetic micrometer-sized particles AL-CTS@MNPs were synthesized from alkaline lignin (AL) and chitosan (CTS) by "one-pot method". The adsorbent presented higher selectivity adsorption effect on anionic dyes than amphoteric and cationic dyes, and even no adsorption effect on cationic methylene blue (MB), which showed that the anionic dyes could be better separated from the other two types of dyes. The adsorption isotherms of the dyes were highly consistent with the Langmuir model, and the maximum adsorption capacity was 329.50 mg/g for methyl orange (MO) and 20.00 mg/g for rhodamine B (RhB). AL-CTS@MNPs showed good adsorption of anionic dyes (MO) in the pH range of 3-9. Meanwhile, the adsorbent AL-CTS@MNPs were also characterized, showing rough surface with specific surface areas of 37.38 m2/g, pore diameter of 95.8 nm and porosity of 17.62 %. The particle sizes were ranged from 800 µm to 1300 µm. The electrostatic attraction and π-π* electron donor-acceptor interactions were the main forces between the adsorbent and anionic dyes. While the electrostatic repulsive force between the adsorbent and the cationic dyes resulted in the non-absorption of MB by AL-CTS@MNPs. Subsequently, the adsorbent maintained a removal rate of >95 % after five adsorption-desorption cycles, demonstrating its excellent stability and recoverability. Ultimately, the prepared AL-CTS@MNPs illuminated good prospect on complex components dyes wastewater treatment.

Carrageenan/calcium alginate composite hydrogel filtration membranes for efficient cationic dye separation.

The development of biopolymer-based filtration systems for water remediation applications is an extremely fascinating area of research. In this paper, we developed a biopolymer-based filtration system using sodium alginate (NaAlg) and carrageenan (Car) for the removal of the toxic cationic dye, methylene blue (MB). The membrane's properties were assessed using FTIR, TGA, UTM, FESEM, EDS, XRD, and water uptake, revealing commendable thermomechanical stability (5.79 MPa), good hydrophilicity, and compatibility. The experimental results further revealed that lambda Car/calcium alginate (λ-Car/CaAlg) exhibited superior dye rejection (100%) and flux (11.67 L m-2 h-1) compared to kappa Car/CaAlg (κ-Car/CaAlg) (99.22% and 11.19 L m-2 h-1) and plain alginate (CaAlg) (99.63% and 9.79 L m-2 h-1). The high MB rejection rate was attributed to the sieving mechanism and electrostatic interaction. A rejection rate of 100% was achieved at an initial MB concentration of 10 mg/L, pressure of 0.1 MPa, pH of 7, and temperature of 25°C. Furthermore, the hydrogel membranes demonstrated excellent recyclability over nine cycles, indicating their potential for water treatment applications.

A floating biosorbent of polylactide and carboxylated cellulose from biomass for effective removal of methylene blue from water.

A floating adsorbent bead was prepared from polylactide (PLA) and maleic anhydride (MAH)-modified cellulose in a one-pot process (OP bead). Cellulose was extracted from waste lemongrass leaf (LGL) and modified with MAH in the presence of dimethylacetamide (DMAc). PLA was then added directly into the system to form sorbent beads by a phase separation process that reused unreacted MAH and DMAc as a pore former and a solvent, respectively. The chemical modification converted cellulose macrofibres (55.1 ± 31.5 µm) to microfibers (8.8 ± 1.5 µm) without the need for grinding. The OP beads exhibited more and larger surface pores and greater thermal stability than beads prepared conventionally. The OP beads also removed methylene blue (MB) more effectively, with a maximum adsorption capacity of 86.19 mg⋅g-1. The adsorption of MB on the OP bead fitted the pseudo-second order and the Langmuir isotherm models. The OP bead was reusable over five adsorption cycles, retaining 88 % of MB adsorption. In a mixed solution of MB and methyl orange (MO), the OP bead adsorbed 96 % of the cationic dye MB while repelling the anionic dye MO. The proposed method not only reduced time, energy and chemical consumption, but also enabled the fabrication of a green, effective and easy-to-use biosorbent.

Enhancing Methylene Blue Removal through Adsorption and Photocatalysis-A Study on the GO/ZnTiO3/TiO2 Composite.

This study focuses on synthesizing and characterizing a graphene oxide/ZnTiO3/TiO2 (GO/ZTO/TO) composite to efficiently remove methylene blue (MB) from water, presenting a novel solution to address industrial dye pollution. GO and ZTO/TO were synthesized by the modified Hummers and sol-gel methods, respectively, while GO/ZTO/TO was prepared using a hydrothermal process. The structural and surface properties of the composite were characterized using various analytical techniques confirming the integration of the constituent materials and suitability for dye adsorption. The study revealed that GO/ZTO/TO exhibits an adsorption capacity of 78 mg g-1 for MB, with only a 15% reduction in adsorption efficiency until the fifth reuse cycle. Furthermore, the study suggests optimal adsorption near neutral pH and enhanced performance at elevated temperatures, indicating an endothermic reaction. The adsorption behavior fits the Langmuir isotherm, implying monolayer adsorption on homogeneous surfaces, and follows pseudo-second-order kinetics, highlighting chemical interactions at the surface as the rate-limiting step. The photocatalytic degradation of MB by GO/ZTO/TO follows pseudo-first-order kinetics, with a higher rate constant than that of GO alone, demonstrating the enhanced photocatalytic activity of the composite. In conclusion, GO/ZTO/TO emerges as a promising and sustainable approach for water purification, through an adsorption process and subsequent photocatalytic degradation.

Easy Preparation of Liposome@PDA Microspheres for Fast and Highly Efficient Removal of Methylene Blue from Water.

Mussel-inspired chemistry was usefully exploited here with the aim of developing a high-efficiency, environmentally friendly material for water remediation. A micro-structured material based on polydopamine (PDA) was obtained by using liposomes as templating agents and was used for the first time as an adsorbent material for the removal of methylene blue (MB) dye from aqueous solutions. Phospholipid liposomes were made by extrusion and coated with PDA by self-polymerization of dopamine under simple and mild conditions. The obtained Liposome@PDA microspheres were characterized by DLS and Zeta potential analysis, TEM microscopy, and FTIR spectroscopy. The effects of pH, temperature, MB concentration, amount of Liposome@PDA, and contact time on the adsorption process were investigated. Results showed that the highest adsorption capacity was obtained in weakly alkaline conditions (pH = 8.0) and that it could reach up to 395.4 mg g-1 at 298 K. In addition, adsorption kinetics showed that the adsorption behavior fits a pseudo-second-order kinetic model well. The equilibrium adsorption data, instead, were well described by Langmuir isotherm. Thermodynamic analysis demonstrated that the adsorption process was endothermic and spontaneous (ΔG0 = -12.55 kJ mol-1, ΔH0 = 13.37 kJ mol-1) in the investigated experimental conditions. Finally, the applicability of Liposome@PDA microspheres to model wastewater and the excellent reusability after regeneration by removing MB were demonstrated.

Bifunctional Fe3O4 nanoparticles as magnet and inducer in bioextruded fabrication of starch-based composite with hierarchical pore architecture.

Starch (St) was used as green and renewable matrix (> 80%, db) for the preparation of Zn-St-MOCP/nFe3O4 composite via bioextrusion. Bifunction of Fe3O4 NPs as magnet and pore-inducer was confirmed and could be more homogeneously embedded in the St-based framework with hierarchical porous structure via SEM-EDS mapping. For the nFe3O4-induced microstructure of Zn-St-MOCP/nFe3O4 composite, submicronic pores and nanopores were observed with Fe3O4 NPs onto the inner surface of micron channels. According to the XPS, XRD, FTIR, TGA analyses, it is probably due to the coordination between Fe3+/2+ and Zn2+/hydroxy groups and the recombination of St chains in crystalline/amorphous zones interfered by Fe3O4 NPs. Saturation magnetization value was measured with an excellent separation behavior. Seven kinetic equations were conducted for the fitting of dye adsorption data. Overall, the nFe3O4-assisted bioextrusion strategy is developed for the continuous fabrication of bio-based materials with rapid magnetic separation and hierarchical-pore architecture promising in practical adsorption.

Selective biosorption mechanism of methylene blue by a novel and reusable sugar beet pulp cellulose/sodium alginate/iron hydroxide composite hydrogel.

A cellulose-based sodium alginate/iron hydroxide (C/SA/Fe) composite hydrogel was fabricated by using epichlorohydrin as cross-linking agent as an effective adsorbent for dye. The physicochemical structure of the C/SA/Fe hydrogel was characterized by SEM, FTIR, XRD and TG. The adsorption performance for the removal of methylene blue (MB) was investigated. In addition, the selective adsorption of cationic dye was also studied. The FTIR analysis revealed that the Fe(OH)3 colloidal particles were successfully combined in the cellulose/sodium alginate hydrogel. The modified hydrogel had better adsorption performance, and the maximum adsorption capacity of C/SA/Fe0.5 for MB was 105.93 mg/g according to the fitting results of adsorption isotherm. The kinetic study showed that the adsorption of MB onto C/SA/Fe was more consistent with the pseudo-second-order model, and was dominated by chemisorption mechanism such as ion exchange or electron sharing. The adsorption data fits well with the Langmuir model. Thermodynamics analysis showed that the MB adsorption by C/SA/Fe was exothermic, spontaneous, favorable and feasible. After five adsorption-desorption cycles, the adsorption capacity was almost unchanged. So, the C/SA/Fe hydrogel is a potential material in the field of the recovery of agricultural by-products or other bio-based cellulose, or environmental protection, etc.

Experimental and Theoretical Insights on Methylene Blue Removal from Wastewater Using an Adsorbent Obtained from the Residues of the Orange Industry.

Chemical and thermochemical transformations were performed on orange peel to obtain materials that were characterized and further tested to explore their potential as adsorbents for the removal of methylene blue (MB) from aqueous solutions. The results show the high potential of some of these materials for MB adsorption not only due to the surface area of the resulting substrate but also to the chemistry of the corresponding surface functional groups. Fitting of the kinetic as well as the equilibrium experimental data to different models suggests that a variety of interactions are involved in MB adsorption. The overall capacities for these substrates (larger than 192.31 mg g-1) were found to compare well with those reported for activated carbon and other adsorbents of agro-industrial origin. According to these results and complementary with theoretical study using Density Functional Theory (DFT) approximations, it was found that the most important adsorption mechanisms of MB correspond to: (i) electrostatic interactions, (ii) H-bonding, and (iii) π (MB)-π (biochar) interactions. In view of these findings, it can be concluded that adsorbent materials obtained from orange peel, constitute a good alternative for the removal of MB dye from aqueous solutions.

Intelligent modeling and experimental study on methylene blue adsorption by sodium alginate-kaolin beads.

As tighter regulations on color in discharges to water bodies are more widely implemented worldwide, the demand for reliable inexpensive technologies for dye removal grows. In this study, the removal of the basic dye, methylene blue, by adsorption onto low-cost sodium alginate-kaolin beads was investigated to determine the effect of operating parameters (initial dye concentration, contact time, pH, adsorbent dosage, temperature, agitation speed) on dye removal efficiency. The composite beads and individual components were characterized by a number of analytical techniques. Three models were developed to describe the adsorption as a function of the operating parameters using regression analysis, and two powerful intelligent modeling techniques, genetic programming and artificial neural network (ANN). The ANN model is best in predicting dye removal efficiency with R2 = 0.97 and RMSE = 3.59. The developed model can be used as a useful tool to optimize treatment processes using the promising adsorbent, to eliminate basic dyes from aqueous solutions. Adsorption followed a pseudo-second order kinetics and was best described by the Freundlich isotherm. Encapsulating the kaolin powder in sodium alginate resulted in removal efficiency of 99.56% and a maximum adsorption capacity of 188.7 mg.g-1, a more than fourfold increase over kaolin alone.

Effective adsorption of methylene blue dye from water solution using renewable natural hydrogel bionanocomposite based on tragacanth gum: Linear-nonlinear calculations.

Today, hydrogels opened new windows to the high-tech due to their amazing features. Thus, we applied hydrogel nanocomposite (HNC) made of tragacanth gum (a kind of polysaccharide) and CaCO3 nanoparticles to remove methylene blue dye (MBD) from the water solution. We used nonlinear and linear isotherms and kinetics as well as thermodynamics to uncover the adsorption mechanism. The results showed that the hydrogel could remove 80% of MBD. Besides, the linear form of the pseudo-second-order kinetic model fits well with the results, showing chemical interactions. We found that this process follows both Sips and Redlich-Peterson models by applying nonlinear and linear isotherm models. The maximum adsorption capacities from nonlinear and linear Sips were 1401 and 2145 mg/g, respectively. Based on the thermodynamic equations, the adsorption of MBD onto HNC was physiochemical and exothermic. According to the phenomenological calculations, diffusion from the bulk (or film diffusion, Df = 1.2 × 10-8 cm2/s) is the primary mechanism.

Methylene blue uptake by gum arabic/acrylic amide/3-allyloxy-2-hydroxy-1-propanesulfonic acid sodium salt semi-IPN hydrogel.

In this study, the capacity of methylene blue (MB) uptake from aqueous solution was investigated using acrylic amide-co-3-Allyloxy-2-hydroxy-1-propanesulfonic acid sodium salt/Gum Arabic semi-IPN hydrogel. The semi-IPN hydrogels were prepared by the classical free radical solution technique. The swelling experiments were carried out gravimetrically and the swelling kinetics parameters were calculated. Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) confirmed the semi-IPN hydrogel formation. The MB uptake was studied by the batch technique and the impact of different conditions was investigated. It was found that the obtained semi-IPN hydrogels gave adsorption capacity for the dye within a range of 101-187 mg g-1 at the initial dye concentration of 100 mg/L. The adsorption kinetics (pseudo-first-order and pseudo-second-order) and the adsorption isotherms (Langmuir, Freundlich, and Temkin equations) were tested and the adsorption data was well described by the pseudo-second-order and Freundlich models, respectively. The maximum adsorption capacity calculated by the Langmuir model (R2 = 0.8718) was 655.2 mg g-1. The thermodynamic study indicated the spontaneity and the endothermic nature of MB adsorption. Furthermore, the usability study showed that the prepared adsorbents could be employed repeatedly for successive 5 cycles of adsorption and desorption.

Preparation of poly(sodium 4-styrene sulfonate) grafted magnetic chitosan microspheres for adsorption of cationic dyes.

A novel adsorbent with high adsorption capacity to remove cationic dyes was synthesized. Sodium 4-styrene sulfonate (SSS) was grafted polymerization on the surface of magnetic chitosan microspheres via -NH2/S2O82- surface initiating system, obtaining MCS-g-PSSS microspheres. The grafted microsphere was characterized by Fourier transforms infrared spectroscopy, X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, vibration sample magnetometer and the Brunauer-Emmett-Teller. Cationic dyes were adsorbed by MCS-g-PSSS and methylene blue(MB) was acted as a typical example. The adsorption performance was explored by varying experimental conditions. The results showed the maximal adsorption capacity was 989 mg/g at pH 1 at 25 °C. The pseudo-second order model was found to be applicable for the adsorption kinetics. The adsorption capacity increased with rising temperature and it decreased owing to adding of ions. The adsorption isotherms were the best fitted by Langmuir. MCS-g-PSSS for MB showed high adsorption capacity due to the strong electrostatic interactions and π-π stacking, which was explained by FTIR and XPS and was verified by DFT calculations. The degree of adsorption spontaneity increased with rising the temperature. The grafted MCS-g-PSSS microspheres had high adsorption capacity for various kinds of cationic dyes and excellent for remove MB in the aqueous solution.

Highly Efficient Methylene Blue Dye Removal by Nickel Molybdate Nanosorbent.

Removing methylene blue (MB) dye from aqueous solutions was examined by the use of nickel molybdate (α-NiMoO4) as an adsorbent produced by an uncomplicated, rapid, and cost-effective method. Different results were produced by varying different parameters such as the pH, the adsorbent dose, the temperature, the contact time, and the initial dye concentration. Adsorbent dose and pH had a major removal effect on MB. Interestingly, a lower amount of adsorbent dose caused greater MB removal. The amount of removal gained was efficient and reached a 99% level with an initial methylene blue solution concentration of ≤160 ppm at pH 11. The kinetic studies indicated that the pseudo-second-order kinetic model relates very well with that of the obtained experimental results. The thermodynamic studies showed that removing the MB dye was favorable, spontaneous, and endothermic. Impressively, the highest quantity of removal amount of MB dye was 16,863 mg/g, as shown by the Langmuir model. The thermal regeneration tests revealed that the efficiency of removing MB (11,608 mg/g) was retained following three continuous rounds of recycled adsorbents. Adsorption of MB onto α-NiMoO4 nanoparticles and its regeneration were confirmed by Fourier transform infrared spectroscopy (FTIR) analysis and scanning electron microscopy (SEM) analysis. The results indicated that α-NiMoO4 nanosorbent is an outstanding and strong candidate that can be used for removing the maximum capacity of MB dye in wastewater.

Synthesis, characterization, and selective dye adsorption by pH- and ion-sensitive polyelectrolyte galactomannan-based hydrogels.

Three novel polyelectrolyte galactomannan hydrogels (PGHs) were fabricated by chemically crosslinking quaternary ammonium galactomannan (QAG) and carboxymethyl galactomannan (CMG), and employed for the removal of Congo Red (CR) and Methylene Blue (MB). Physicochemical characterization revealed that the PGHs are chemically and physically crosslinked. The PGHs are pH- and ion-sensitive, and their physical crosslinking can be destroyed by artificial urine; water swelling capacity (100.6-321.9 g/g dry gel) and artificial urine swelling capacity (35.9-80.5 g/g dry gel). The adsorption of CR and MB was studied and found to be pH-dependent and selective. The maximum adsorption capacities of CR and MB on the QAG and CMG gels are 1441 and 94.52 mg/g, respectively, and their adsorption kinetics and isotherm behavior obey the pseudo-second-order kinetics model and Langmuir isotherm model, respectively. The adsorption mechanism is dominated by electrostatic interactions and hydrogen bonding. Further, the PGHs have excellent salt resistance and are reusable.