Adsorption Of Methylene Blue Dye Research Articles

Sustainable Methylene Blue dye removal with activated carbon from Prosopis juliflora stem

This study addresses the environmental challenge posed by the invasive Prosopis juliflora plant by converting its stem into activated carbon for the adsorption of Methylene Blue dye from water. The goal is to create an effective and sustainable wastewater treatment solution. Prosopis juliflora stems were harvested, cleaned, dried, carbonized, and activated with zinc chloride to create Prosopis Juliflora Stem Activated Carbon. This activated carbon was characterized using Brunauer-Emmett-Teller surface area analysis, Fourier transform infrared spectroscopy, and scanning electron microscope imaging. Results revealed a significant surface area of 158.107 m2/g and the presence of functional groups essential for adsorption processes. Batch adsorption experiments were conducted to determine the efficiency of activated carbon in removing Methylene Blue dye at various dosages and contact times. The highest adsorption efficiencies were 73.5% at 80 min, 90.1% at 60 min, and 90.65% at 50 min for dosages of 80, 100, and 120 mg, respectively. These findings show that Prosopis Juliflora Stem Activated Carbon is highly effective at removing Methylene Blue dye, providing a cost-effective and environmentally friendly method of wastewater treatment.

Methylene Blue Adsorption Using Boric Acid Functionalized Activated Carbon: Kinetics, Isothermal, and Thermodynamic Studies

AbstractIn this study, the activated carbon (AC) was prepared from Sesbania sesban plant stem. Boric acid (H3BO3) was used as an activating agent. During calcination, the optimized temperature was kept upto 500 °C for 2 h. The prepared adsorbents were characterized using various techniques such as FT‐IR, scanning electron microscopy, energy dispersive x‐ray spectroscopy, and thermogravimetric analyzer. The prepared adsorbents were used for the removal of methylene blue (MB) dye adsorption. The adsorption experiments were conducted at different pHs such as (2–11), doses (0.0025–0.020 mg), times (30–300 min), MB initial concentrations (100–600 mg L−1), and temperatures (298–318 K), respectively. The maximum MB uptake capacity of the prepared adsorbent was 1380 mg g−1 under optimized adsorption conditions. Furthermore, the kinetic study is well described by pseudo‐second order, whereas the isothermal study showed the Freundlich isotherm was better followed by the equilibrium data. Based on thermodynamic studies, the negative values of ΔG° and ΔH° revealed that the MB adsorption process is spontaneous and exothermic in nature. However, the negative ∆Sxg° value indicates that solid‐solute interaction decreased randomness in the adsorption systems. The overall studies of AC showed that it was better to remove MB from an aqueous solution.

Preparation and characterization of oat hulls-filled-sodium alginate biocomposite microbeads for the effective adsorption of toxic methylene blue dye

In this work, the performance of oat hull-filled sodium alginate (SA-O) biocomposite microbeads in the adsorptive removal of methylene blue (MB) dye was examined. First, oat hulls were pulverized and biocomposite gels containing different weight ratios of oat hulls (10 %, 20 %, and 30 %, concerning the SA amount) were prepared by dispersing them in SA solution by ultrasonic homogenization method. Finally, gels were cross-linked by dropping into a 2 % CaCl2 solution. The study revealed that the optimal adsorbent dosage was 0.025 g/50 mL, pH was roughly 6–8, and the contact time was 120 min. According to isotherm models, the non-linear Sips and Langmuir model was more appropriate compare to other isotherms from error analysis, with a maximum adsorption capacity of 687.65 mg/g and 757.57 mg/g at 298 K, respectively. Furthermore, the non-linear kinetic data and error analyzes demonstrated that the process followed the pseudo-second-order kinetic. The adsorption process was exothermic (∆H°=−17.71 kJ/mol) and spontaneous (∆G°=−26.23 kJ/mol) at 298 K, based on thermodynamic characteristics. Furthermore, reusability investigations demonstrated that the adsorbent retained its performance with no major changes in characteristics. This work reveals that highly efficient, low-cost, sustainable, and eco-friendly SA-O composites with properties might be useful adsorbents for cationic dye adsorption.

Lemon Peel‐Extracted Recyclable Copper Oxide Nanoparticles for Methylene Blue Dye Adsorption: Optimization, Isotherms, Kinetics, Thermodynamics, and Reusability Study

AbstractResearchers are exploring sustainable methods for synthesizing metal oxide nanoparticles to address wastewater pollution, which poses a global threat to aquatic life and human health. The present research aims to biosynthesize recyclable Lemon peel‐extracted copper oxide nanoparticles (CuO NPs) to remove methylene blue dye via adsorption. Our approach involves a comprehensive range of techniques, such as FTIR, XRD, SEM‐EDX, Zeta potential, and UV‐VIS, to thoroughly characterize the NPs. SEM analysis confirmed that the CuO NPs, with an average size of 64.5 nm and a nearly spherical shape, exhibited a zeta potential value of – 16.34, indicating their relative stability. Optimized conditions for the 92.20% adsorption efficiency for methylene blue dye were pH at 6, contact time of 90 min, 0.06 g of adsorbent dose, 10 ppm dye conc., and Temp. 27 °C. Langmuir 1‐based maximum adsorption capacity (qm) was 617.28 mg/g for CuO NPs. Langmuir 1 and Freundlich are the most suitable isotherm models for experimental data, supporting Physi‐chemisorption and chemisorption as rate‐limiting steps in the exothermic adsorption process. A reusability study of up to three cycles proved the sustainability of the materials.

Electrospinning of Sodium Alginate/Copper Oxide Nanofibrous Composite Membrane and Its Application of Cationic Dye Adsorption

AbstractDye wastewater is becoming one of the most significant sources of water pollution, and its impact on human survival is immeasurable. In this study, we successfully synthesized a nanofiber membrane with environmentally friendly and efficient properties using electrospinning of a mixture of sodium alginate (SA) and copper oxide (CuO) nanoparticles, aimed at effective dye removal. The adsorption performance of the SA/CuO nanofiber membrane was evaluated using the cationic dye methylene blue (MB). The maximum adsorption capacity of the nanofiber membrane was increased significantly with the addition of CuO nanoparticles, reaching a maximum value of 1633.4 mg g−1, almost twice as much as that of pure SA membrane. The adsorption kinetics follows the pseudo‐second‐order model, where chemisorption acts as the rate‐limiting step. The adsorption isotherm data indicate that the adsorption is monolayer. The nanofibrous membranes showed better dye removal under an alkaline environment. After four cycles of adsorption/desorption, the MB removal efficiency remained at 70.1% of the original adsorption capacity. The addition of CuO nanoparticles facilitated the adsorption of MB dyes, while the form of the nanofibrous membrane is easily recoverable and reusable. Therefore, the as‐prepared SA/CuO nanofibrous composite membrane is a potentially favorable adsorbent material for wastewater treatment applications.

Kinetic and thermodynamic study of the adsorption isotherm of methylene blue dye from aqueous solutions by activated carbon

The efficiency of activated carbon in wastewater as a powerful blue dye remover has been studied. In this work, activated carbon manufactured from Sidr leaves was used to adsorb methylene blue dye. The factors affecting adsorption were studied, such as the weight of the adsorbent, temperature, contact time, and initial concentration of the dye, and the optimal conditions for adsorption were determined according to the experimental results. It was evident from the experimental results obtained that the removal efficiency increases with the increase of both the weight of the adsorbent material and the contact time. It was observed that the adsorption process was possible, spontaneous, and exothermic in the temperature range (293-333 K), and this is what determined the thermodynamic variables ΔG°, ΔH°, and ΔS°. The Langmuir, Freundlich, and Timken isotherms were used to examine the experimental equilibrium data. To follow the adsorption process, two logical models were chosen, represented by the Elovage equation and diffusion.

Adsorption Kinetic, Isotherm and Mechanism Study of Xanthate-Modified Neem Leaf Powder as an Efficient Adsorbent for Methylene Blue Dye

Adsorption Kinetic, Isotherm and Mechanism Study of Xanthate-Modified Neem Leaf Powder as an Efficient Adsorbent for Methylene Blue Dye

Adsorption of methyl orange and methylene blue from aqueous solutions on pure bentonite: statistical physical modeling provides an analytical interpretation.

This study investigates the adsorption of methylene blue (MB) and methyl orange (MO) dyes from aqueous solutions using purified Moroccan bentonite, being mainly composed of silica and alumina, in the form of quartz and cristobalite. The temperature controls the adsorption capacity for the kinetics, increasing 5.08% (from 295.1 to 310.1 mg/g) for the MB and 55.47% (from 86.8 to 134.9 mg/g) for the MO. It was discovered that the pseudo-second-order model, with a low Bayesian criterion indicator of 12.72 and R2adj > 0.996, was the best suitable for explaining both systems. The adsorption isotherm, experimental data indicate that both systems follow the Langmuir isotherm. At lower temperatures, 298.15 K 1.22 molecules are adsorbed per site. However, at a higher temperature of 328.15 K, the number of molecules is less than a unit of 0.68. As for MO, the number of molecules remains above 1.4 per site for all the temperatures studied. The endothermic nature of the system is indicated by the observation that the adsorption energy tends to grow for both systems: for the MB, it increases from 18.85 to 21.26 kJ/mol, and for the MO, it increases from 14.83 to 19.01 kJ/mol. Last, thermodynamic functions indicate that maximum entropy is reached around the half-concentration saturation at 25 and 124 mg/L, which is the maximum energetic concentration of the system. The same results were obtained for Gibbs free energy, where the maximum energy found was - 5.39 × 10-18 kJ/mol for the MB and - 1.99 × 10-18 kJ/mol for the MO at 328.15 K.

Advanced nano modification of ecofriendly glauconite clay for high efficiency methylene blue dye adsorption

This research focuses on the utilization of nano glauconite clay as an environmentally friendly sorbent for the removal of cationic dyes, particularly Methylene Blue (MB), from polluted water. The glauconite clay was sourced from the El Gidida region of Egypt and subjected to grinding in a laboratory-type ball mill to ensure homogeneity and increase the active sites available for the adsorption process. The resulting ball milled nano clay (BMNC) was characterized using techniques such as X-ray fluorescence (XRF), Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). The concentration of MB dye was monitored using UV–Vis spectroscopy to assess the adsorption capacity of BMNC under various conditions including pH, time, dose, and temperature. The optimal conditions for the adsorption process were determined to be a pH range of 7–8, a contact time of 60 min, and a dose of 200 ppm, resulting in an adsorption capacity of 128 mg/g. This process demonstrated both low cost and high speed. The adsorption mechanism of MB on the BMNC surface was evaluated through kinetics, adsorption isotherms, and thermodynamics. The experimental data indicated an endothermic, spontaneous, and thermodynamically favourable adsorption process, which was further supported by simulated modelling results using Forcite program. The in-silico data aligned well with the experimental findings. Additionally, the study assessed the interference of salts, metal ions, and other dyes on MB adsorption onto BMNC, showing promising results. These findings strongly support the effectiveness of our sorbent substrate under challenging conditions.

The Effects of Hydrothermal Temperatures on ZnO-Bentonite Composite Synthesis on Adsorption and Photodegradation of Methylene Blue Dye

This study explores the influence of hydrothermal temperatures on the synthesis of ZnO-Bentonite composites and their efficiency in the adsorption and photodegradation of Methylene Blue dye. ZnO nanoparticles were integrated into Na-Bentonite, with composites synthesized at hydrothermal temperatures of 100°C and 200°C. Various characterization techniques such as XRD, FTIR, UV-Vis DRS, TG-DTA and BET were utilized to analyze the structural and thermal properties. The results show that the composite synthesized at 200°C exhibits superior performance, with a maximum adsorption capacity of 120.48 mg/g at 50°C, significantly higher than the 49.26 mg/g achieved by the composite synthesized at 100°C. Moreover, the enhanced crystallinity and increased surface area, as evidenced by a 16 nm crystallite size at 100°C and 22 nm at 200°C, led to improved photocatalytic activity. The research concludes that higher hydrothermal temperatures improve both adsorption and photodegradation efficiency, making the composite synthesized at 200°C more effective for environmental applications.

Waste biomass-based graphene oxide decorated with ternary metal oxide (MnO-NiO-ZnO) composite for adsorption of methylene blue dye

In this study, a novel approach for the removal of methylene blue (MB) dye is effectively illustrated by using biomass based composite adsorbent. The investigation employed areca nut husk (AH) to produce graphene oxide (GO) by a single step calcination method. Thereafter, AH-GO was incorporated by using ternary metal oxide (TMO) via hydrothermal treatment. The developed AH-GO@MnO-NiO-ZnO composite was characterized by various analytical techniques, including FT-IR, XRD, FESEM, HRTEM, BET surface area and Raman spectroscopy which exhibited promising properties for dye adsorption. To study the adsorption efficiency of prepared composite, optimization experiments were performed for adsorbent dose, initial dye concentration and contact time. The optimized parameters during adsorption phenomenon were found to be 0.5g/L of dose, 20mg/L of initial concentration and 180min of time exhibiting removal efficacy of 93.05 ± 0.93%. Moreover, adsorption isotherm and kinetic models were analysed to explore the adsorption behaviour of AH-GO@MnO-NiO-ZnO towards MB dye. The adsorption isotherm and kinetic studies followed Langmuir isotherm model and pseudo-second-order (PSO) model respectively. AH-GO@MnO-NiO-ZnO has demonstrated a maximum adsorption capability of 127.06mg/g. These findings collectively underscore the potential of AH-based adsorbent as a viable, inexpensive, and environment friendly for the treatment of wastewater contaminated with MB dye.

Study of Methylene Blue dye adsorption onto biochar derived from Austrocylindropuntia subulata plant

Abstract The reuse of treated wastewater in drinking water supply and irrigation emerges as a potent solution to address water scarcity. Recent years have witnessed a growing interest in wastewater treatment using ecological, non-toxic, and biodegradable materials. In this study, Austrocylindropuntia subulata was employed for the first time to adsorb a synthetic dye, methylene blue. The feedstock underwent pyrolysis followed by chemical activation using orthophosphoric acid, resulting in the formation of biochar. Characterization through SEM, XRD, and FTIR analyses reveals that the biochar surface possesses functional groups such as alcohol and amide. Microscopic images highlight a diverse array of particle shapes and sizes, along with varying proportions of calcium and carbon in the biochar. Adsorption tests demonstrate that the optimal mass of biochar is 0.5g, ensuring a remarkable 99.8% adsorption of methylene blue dye within a 30 minutes contact time. The findings of this study underscore the compelling adsorbent capabilities of biochar derived from the Austrocylindropuntia subulata plant, suggesting its potential as a valuable resource in wastewater treatment.

Optimization study of methylene blue dye adsorption on Chamaerops humilis fibers biosorption using a central composite design

This research explores the effectiveness of Chamaerops humilis (CH) fibers as a biosorbent for the adsorption of Methylene Blue (MB) dye from aqueous solutions. The fibers were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR). To optimize the dye removal process, a Design of Experiments methodology, specifically Central Composite Design (CCD), was applied. Factors such as solution pH, adsorbent dosage, contact time, and temperature were varied. The CCD analysis identified the optimal conditions for maximum removal efficiency (99.87 %) of a 10 mg/L MB solution, which were: 1.06 g/L of CH fiber dosage, pH 9.6, and a contact time of 60 min. The adsorption process aligned well with a pseudo-second-order kinetic model, and the maximum adsorption capacity of CH fibers was determined to be 9.422 mg/g. Thermodynamic parameters, including Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) changes, were calculated, confirming that the adsorption is spontaneous and endothermic. The study highlights the potential of Chamaerops humilis fibers as an efficient and eco-friendly adsorbent for MB dye removal, offering a sustainable and cost-effective solution for wastewater treatment, particularly in industrial effluent management.

Valorization of the performance of novel and natural sodium alginate/pectin/Portulaca oleracea L. ternary composites in the adsorption of toxic methylene blue dye from the aquatic environment

This research introduces the development of a novel, sustainable, cost-effective, and eco-friendly sodium alginate (SA)-pectin (P) ternary composite, enhanced with Portulaca oleracea L. (PO) additive, which has been thoroughly investigated for its efficacy in removing hazardous methylene blue (MB) dye from wastewater. The selectivity studies using various cationic and anionic dyes were conducted. The composite microbeads that were generated underwent characterization using FTIR-ATR, SEM, XRD, zeta potential, and pHpzc analysis. Subsequently, the most favorable parameters for adsorption, including initial pH (2–12), contact time (0–180 min), adsorbent dosage (0.01–0.20 g), and temperature (298–318 K), were identified. The effect of monovalent and divalent salt concentrations on adsorption process was evaluated. The adsorption data were utilized in several isotherm (Langmuir, Freundlich, D-R, and Temkin) and kinetic (pseudo-first-order and pseudo-second-order) models. According to the Langmuir isotherm model was calculated the adsorption capacity at 298 K is 709.22 mg/g for SA/P/PO30 composite microbeads. The process of adsorption was seen to conform to a pseudo-second-order kinetic model. The results revealed that the process was both exothermic (∆Ho=−10.42kJ/mol) and spontaneous (∆Go=−26.04kJ/molat298K). Moreover, reusability analyses demonstrated that the composite microbeads that were created may be utilized several times, even after the 5th cycle. The results indicate that the developed composite microbeads have the potential to serve as an effective and inexpensive adsorbent for eliminating cationic contaminants from a wastewater.

Examining the influence of sintering temperatures on the efficiency of 3D-printed natural zeolite for methylene blue dye adsorption

Additive manufacturing technology, with its potential for improved material efficiency, cost reduction, and capability to fabricate complex structures, is increasingly being leveraged in environmental engineering applications. This study harnesses this technology for fabricating natural zeolite adsorbents using an extrusion-based 3D printer, examining the influence of different sintering temperatures (300, 600, 900, and 1200 °C) on the adsorbents' properties. The study finds that samples sintered at 300 °C disintegrated in water, while those at 1200 °C underwent melting, changing their shape. Focus was then shifted to samples sintered at 600 °C (3D-Ze-600) and 900 °C (3D-Ze-900), with the former displaying a remarkable methylene blue (MB) adsorption efficiency of 82.5%, significantly higher than the latter's 20.1%. This disparity in adsorption performance is closely linked to the difference in porosity; the 600 °C samples exhibited a notably higher apparent porosity, which was instrumental in their enhanced adsorption capability. In contrast, the 900 °C samples, despite their lower porosity, showed diminished adsorption efficiency. XRD analysis further revealed that the superior performance of the 600 °C samples could be attributed to their preserved crystalline structure, which was altered in the 900 °C samples. These findings highlight the critical role of sintering temperature in determining the structural and functional properties of 3D-printed zeolites, demonstrating their potential as efficient adsorbents in wastewater treatment and offering valuable insights for optimizing the fabrication process for environmental applications.

Poly(methyl methacrylate) functionalized graphene oxide/CuO as nanocomposite for efficient removal of dye pollutants

In this research, the use of a three-component nanocomposite of graphene oxide-methyl methacrylate and copper(II) oxide (PMMA-GO-CuO) was investigated. The aim of synthesizing this nanocomposite is to removal dye pollutants, specifically methylene blue (MB) and methyl orange (MO), which are commonly used in dyeing industries, through adsorption. The study focuses on creating GO-CuO and PMMA-GO-CuO nanocomposites as effective adsorbents. A simple and quick method led to the development of the PMMA-GO-CuO nanocomposite, which shows enhanced physical and chemical properties. Key materials include graphene oxide, methyl methacrylate, and copper(II) oxide nanoparticles. Characterization techniques such as FT-IR, XRD, SEM, and TGA were used to analyze the nanocomposite. Results indicate that dye adsorption is more effective at lower pH levels, suggesting that the PMMA-GO-CuO nanocomposite can efficiently remove dyes from industrial wastewater. The experimental data showed that the Langmuir isotherm model accurately represented the equilibrium adsorption, with maximum capacities of 285.71 mg g−1 for methylene blue and 256.41 mg g−1 for methyl orange, indicating a single layer of adsorption. The kinetics followed a pseudo-second order model, suggesting that the adsorption process involves chemical bonding. Additionally, thermodynamic parameters (ΔG°, ΔH°, and ΔS°) indicated that the adsorption is spontaneous. The adsorption mechanism involves hydrogen bonding, π-π interactions, and electrostatic interactions. This study investigates how factors like pH, temperature, contact time, and dye concentration affect the adsorption of methyl orange and methylene blue dyes. A PMMA-GO-CuO nanocomposite was used, achieving 84% removal of MB and 35% removal of MO from industrial wastewater. This study highlights the promising potential of PMMA-GO-CuO nanocomposite as an effective material for the removal of dye pollutants from industrial wastewater. The results showed that the graphene oxide in the composite is effective for removing cationic dyes due to its negative charge. Further research will focus on the optimization of the synthesis process with the aim of achieving competitive performance of this nanocomposite on a large scale. These findings not only advance the field of nanocomposite materials but also provide a practical solution to an important environmental issue, demonstrating the innovation of the present study in the literature.

Application of Anionic Hydrogels from Date Palm Waste for Dye Adsorption in Wastewater Treatment.

This work aimed to develop an anionic cellulose nanofiber (CNF) bio-adsorbent from date palm tree waste and to investigate its removal efficiency compared to cationic methylene blue dye from contaminated water. Date palm pulp was first prepared from date palm leaves through acid hydrolysis using H2SO4, followed by hydrolysis in a basic medium using KOH, in which the process completely removed the components of hemicellulose, lignin, and silica. To obtain anionic CNF, the resulting pulp was further treated with H2SO4, followed by centrifugation. Biogel formation of the CNF suspension was promoted by sonication, where its removal efficiency of methylene blue dye was studied as a function of dye concentration, temperature, contact time, and pH value. In this work, we investigated two isotherms, i.e., Langmuir and Freundlich. The Langmuir model's consistency with the experimental data suggests that the adsorption of methylene blue dye onto CNF is monolayer and surface-limited. The reported maximum removal efficiency of 5 mg/g at 60 °C indicates the optimal temperature for adsorption in this specific case. Additionally, a pseudo-second-order model and Elovich model were also utilized to obtain a better understanding of the adsorption mechanism, in which we found not just physical adsorption but also an indication of a chemical reaction occurring between methylene blue dye and CNF. According to the results, that pseudo-second-order model's consistency with the experimental data suggests that the adsorption of methylene blue (MB) onto CNF is rate-limiting step involving chemisorption between the two. The study reveals that CNF adsorbents derived from renewable natural waste sources such as date palm leaves can be effective in removing cationic contaminants such as methylene blue dye.

Adsorption of Methylene Blue Dye by Modified Reed Activated Carbon: Adsorption Optimization and Adsorption Performance

Adsorption of Methylene Blue Dye by Modified Reed Activated Carbon: Adsorption Optimization and Adsorption Performance

Comparative performance of fruit peel materials for methylene blue dye adsorption

Comparative performance of fruit peel materials for methylene blue dye adsorption

Methylene blue sorption performance of lignocellulosic peach kernel shells modified with cellulose derivative chitosan as a new bioadsorbent

In this study, adsorption isotherms (Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich) and thermodynamic properties of cationic methylene blue (MB) dye adsorption onto chitosan-coated peach kernel shell waste (CTS-PKSh) from wastewater were investigated. CTS was cross-linked with citric acid (CA) and glutaraldehyde (GA). The adsorbents were characterized by FE-SEM/EDS, FTIR, and particle size distribution. MB adsorption behavior onto the biosorbents was investigated concerning parameters such as adsorbent dosage (0.8–8 g/L), time (0–540 min), pH (3−10), initial dye concentration (50–700 mg/L), and temperature (25–55 °C). The Langmiur qmax and experimentally qe MB adsorption capacities of the new adsorbents were found to be 227.27 and 201 mg/g for CA cross-linked CTS-PKSh (CA@CTS-PKSh) and 111.12 and 96.5 mg/g for GA cross-linked CTS-PKSh (GA@CTS-PKSh), respectively. The results of thermodynamic analysis showed that adsorption was feasible, exothermic, and spontaneous. According to adsorption and recyclability results, CA@CTS-PKSh was more effective for MB removal at a 2 g/L adsorbent dose for an initial dye concentration of 100 mg/L, 25 ± 1 °C, contact time 60 min, and pH 7.