Initial Methylene Blue Concentration Research Articles

Assessment of the adsorption capacity of biochar samples obtained from agricultural biomasses

The study consists of adsorption tests on two samples of biochar, obtained from rice husk and coconut fiber biochar biomass, as well as a sample of charcarbon, both prepared under different conditions: macerated and non-macerated; impregnation with and without HCl and H3PO4; and washing or not with deionized water after impregnation. The test was performed in duplicate, for 30 min, with masses of 0.5 g; 0.3 g; 0.1 g; and 0.05 g, and an initial methylene blue concentration of 0.01 g∙L-1. The study was carried out with the objective of identifying, in the analyzed samples, the material with the greatest adsorption capacity of methylene blue dye, comparing the data with commercial activated carbon. The results identified removal above 70 % in both types of biochars, suggesting the feasibility of application as an adsorbent material to remove organic contaminants. The sample that most closely resembled the removal percentage of commercial activated carbon (98.84 %) was that of biochar obtained from coconut fibers, with 91.71 %. Thus, the research showed promise in studying the application and valorization of biochars, produced from agro-industrial waste, in adsorption processes.

Bio-sorption of methylene blue using Datura stramonium leaves as adsorbent

Present study was accomplished to prospect the viability of using the Datura stramonium leaves powder (DS) as an adsorbent to remove the methylene blue from aqueous solution. The physico-chemical characteristics of the studied adsorbent were examined. The optimum parameters such as contact time, particle size, absorbent dose, initial methylene blue concentration, and pH were investigated by performing batch experiments models. The kinetics and the isotherms adsorption were evaluated by varying the initial concentration and using the optimum parameters. The optimum of contact time is 30min, with a removal capacity of 89.60 %. The optimal adsorbent concentration to reach the maximum removal of methylene blue (89.54 %) is 18 g/L. An initial methylene blue concentration of 50 ppm is ideal to reach the maximum capacity of removal (92.72 %). The optimum particle size is 80 mm. The kinetics of the adsorption process are in accordance with the pseudo-second order model. Experimental values of the adsorption capacity are close proximity to the optimum values predicted by the pseudo-second order model. Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Harkin-Jura and Hasley isotherms were applied to represent the data obtained from the adsorption studies. The highest R2 values were related to Freundlich, Dubinin-Radushkevich and Hasley isotherm models.

Improving Photocatalytic Efficiency with Titanium Dioxide Quantum Dots

Titanium dioxide quantum dots (TiO2-QDs), synthesized using a microwave-assisted method, represent a significant advancement in photocatalysis, particularly in the treatment of environmental pollutants. This study focuses on TiO2-QDs synthesized at 200°C for a duration of 5 minutes, using titanium butoxide as a precursor. Characterization through TEM, XRD, PL, and UV-Vis-DRS analyses revealed uniform quantum dots with an average size of 5.28 nm, a bandgap energy of 3.22 eV, and a crystalline anatase phase, indicative of high photocatalytic activity. Notably, these TiO2-QDs demonstrated exceptional performance in degrading methylene blue (MB) in water, achieving a remarkable treatment efficiency of 97.6% in 120 min, significantly outperforming both conventional titanium dioxide nanoparticles and commercial titanium dioxide materials. The reaction conditions were evaluated based on factors such as catalyst dose, initial MB concentration, and pH. The results indicate that optimal degradation efficiency of MB was achieved at a pH of 7, with a catalyst dose of 0.15 g/L and at a low MB concentration. The efficiency slightly decreased to 94.5% after five reuse cycles, emphasizing its significant reusability and stability. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Cnicus Benedictus roots as a low-cost adsorbent for methylene blue dye removal from aqueous solution: kinetic and equilibrium studies

In this research, Cnicus Benedictus roots powder (CBRP) was utilized as a low-cost adsorbent for removing methylene blue (MB) as a cationic dye from aqueous solution. Characterization of CBRP by Boehm titration method, Fourier transform infrared (FT-IR) and environmental scanning electron microscope (ESEM) indicates the presence of different types of functional groups and a very rough surface filled with cavities, suitable for MB adsorption. The effect of various parameters such as CBRP dose (0.2–2 g/1L), contact time (0–180 min), initial pH (1–10), coexisting anions/cations and the initial MB concentration (100–500 mg L−1) on MB adsorption were examined, the results showed that MB uptake depends on the pH of solution, the electrostatic attraction forces, the formation of H-bonds and π–π interactions are the possible CBRP–MB interaction mechanisms. Adsorption kinetic of MB on CBRP was best represented by linear and non-linear form of the pseudo-second order model. The experimental equilibrium data were best described by linear and non-linear forms of Langmuir and Redlich–Peterson isotherm models (R 2> 0.98) with a maximum MB adsorption capacity of 85.47 mg g−1 at 25 °C, the adsorption efficiency R (%) was greater than 90 (%). MB adsorption-desorption experiments showed the reusability of CBRP for five consecutive cycles. According to the obtained results, CBRP can be used as a natural adsorbent material for cationic dyes removal from aqueous solution.

CARBON-SILICA COMPOSITE AS ADSORBENT FOR REMOVAL OF CATIONIC DYE (METHYLENE BLUE)

The aim of this research was to synthesize carbon-silica composite (CSC) as an adsorbent for cationic dye removal from wastewater. Molasses, a by-product of the sugar industry, was successfully utilized to prepare CSC by sol-gel method with tetraethoxylsilane (TEOS) as silica source. The physicochemical properties of the composites were studied by N2 adsorption, FTIR and TGA. The highest specific surface areas of CSC was 144 m2/g at a molasses/TEOS ratio of 0.8, with a mesopore volume of 83% and average pore width of 9.71 nm. This optimal CSC was evaluated for methylene blue (MB) adsorption using batch experiments under varying adsorption times and initial MB concentrations. Adsorption equilibrium was reached within 14 h and the pseudo-second order equation provided the adequate fit for the kinetic studies, suggesting that dye adsorption was limited by chemisorption. The equilibrium data were best described by the Sips model with a maximum adsorption capacity of 180.22 mg/g. The CSC derived from molasses is considered a potentially promising adsorbent for cationic dye removal in wastewater.

Sugarcane peel ash as a sorbent for methylene blue

Sugarcane peel waste (SPW) modified by combustion was used as a sorbent for methylene blue (MB) in aqueous medium under the influence of parameters such as pH of the medium, initial MB concentrations, contact time, SPW dosage, and temperature using batch experiments. The microstructure of the adsorbent was analyzed using Fourier infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), and X-ray diffractometer (XRD). The quantity (mg/g) of adsorbed MB increased with increased contact time, rise in dye concentration, as well as the solution pH. Similarly, the temperature of the system improved the sorption effectiveness with maximum sorption capacity of 65.4 and 81.2% at 45 °C and 55 °C for USPW and MSPW, respectively. At an initial MB concentration of 100 mg/L, temperature of 45 °C and 55 °C, pH of 4, and reaction times of 80 and 60 min for unmodified sugarcane peel waste (USPW) and modified sugarcane peel waste (MSPW), respectively, optimal MB adsorption of 22.6 and 33.2 mg g-1, respectively, was achieved.

Methylene blue adsorption by chemical-activated Trichanthera gigantea leaf

ABSTRACT This study investigated the potential of NaOH-treated Trichanthera gigantea leaf (TGL) powder as a sustainable, low-cost biosorbent for methylene blue (MB) removal from wastewater. Characterization using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller, and energy-dispersive X-ray spectroscopy (EDX) techniques confirmed favorable morphology, identifying micropores, suitable functional groups, notable surface area, pore volume, and elemental diversity. Batch experiments systematically investigated the influence of operational parameters, including contact time, initial MB concentration (5–35 mg/L), pH (2–10), and biosorbent dosage (2–10 g/L) on adsorption performance. The Langmuir isotherm model best represented the experimental data (R² values of 0.993 and 0.9725), indicating favorable adsorption (RL < 1) and maximum MB adsorption capacities of 0.822 and 0.330 mg/g for treated and untreated TGL, respectively. Statistical analysis (ANOVA) results further identified the most significant factors influencing MB biosorption. These findings highlight the potential of NaOH-treated TGL powder as an effective and eco-friendly solution for removing MB dye from industrial effluents, contributing to sustainable wastewater treatment and environmental protection.

Scale-bridging And Modelling Study of Graphene Shell Composite Adsorption for Dye Removal in Water Treatment

Continuous fixed-bed adsorption is a cost-effective water-treatment method for dye removal. This research examined parameters such as bed heights (5, 7, and 9cm), initial methylene blue (MB) concentrations (10, 15, and 20mg/L), and feed flow rates (8, 10, 12 and mL/min) on fixed-bed adsorption performance. Our findings showed that the performance was improved under longer exhaustion times not only with increasing column bed heights, but also with decreasing initial MB concentrations and feed flow rates. Of note, the Thomas and Yoon-Nelson models accurately described MB adsorption in a fixed-bed column, with R2 values from 0.7525 to 0.9833. Response surface methodology via central composite design optimized column bed heights and feed flow rates on the duration required to achieve 50% of column breakthrough. The coefficient of determination (R2) and analysis of variance demonstrated the significance of the Two Factor Interaction (2FI) model in fitting the actual values. The optimum conditions were determined to be as follows: a bed height of 5cm; a feed flow rate of 8mL/min; and a duration of 54.74min to achieve 50% of column breakthrough. Lastly, a confirmatory test further verified the precision of the proposed optimum conditions with an error of only 0.02%.

Adsorption Capacity and Efficiency of Composite Thin Sheet Made of Chitosan-Activated Carbon on The Adsorption of Methylene Blue

Abstract Methylene blue (MB) is a waste dye produced by textile industries. One way to reduce MB in polluting the environment is using MB adsorbent materials, such as chitosan (CS)-based composites. This research aims to investigate the adsorption capacity and efficiency of chitosan-activated carbon composites (CS-AC), which are in the form of thin sheets, on MB adsorption. The composite was made by manually mixing the chitosan and activated carbon, and then the mixture was poured into a dish and dried at around 50 °C until a dry, thin sheet was formed. The composites were prepared with varying activated carbon mass concentrations (25%, 50%, 75%, and 100% of chitosan mass). The MB adsorption measurements were carried out using UV-Vis spectroscopy. Adsorption capacity and adsorption efficiency increase with increasing activated carbon content, and the composite containing activated carbon mass 100% of chitosan mass shows the highest values, namely 11.51 mg/g and 95.93%, respectively. Furthermore, the values of adsorption capacity and adsorption efficiency are also influenced by the initial MB concentration and mass of the adsorbent. The adsorption capacity increases with increasing initial MB concentration but decreases with increasing adsorbent mass. Adsorption efficiency increases with increasing initial MB concentration and adsorbent mass.

Chitosan‐Carbon Aerogel for Efficient Removal of Methylene Blue Dye: Synthesis, Characterization, Adsorption Mechanism and Antimicrobial Therapies

AbstractChitosan‐carbon aerogel was synthesized via a facile and eco‐friendly method and characterized for its structural and morphological properties. The composite exhibits remarkable adsorption kinetics and a high potential for removing Methylene Blue (MB) dye, attributed to its enhanced surface area, porous structure, and active functional groups. The adsorption capacity of chitosan‐carbon aerogel increased from 38 to 86.8 mg/g as the pH was raised from 2 to 7. The maximum MB adsorption capacity increased from 22 to 632 mg/g as the initial MB concentration increased from 25 to 2000 mg/L. The saturation adsorption capacity of the chitosan‐carbon aerogel was 668 mg/g. After five reuse cycles, the removal efficiency dropped from 89 % to 73.1 %. Antibacterial tests showed that the width of the inhibition zone for S. enterica was 16.2 ± 0.38 mm, indicating similar antibacterial activity for both chitosan and chitosan‐carbon aerogels. These findings underscore the potential of chitosan‐carbon aerogel as a sustainable and cost‐effective solution for dye removal in wastewater treatment.

Box-Behnken design optimization of 2D Ti3C2Tx MXene nanosheets as a microwave-absorbing catalyst for methylene blue dye degradation

The 2D MXene Ti3C2Tx was synthesized from the precursor MAX phase Ti3AlC2 by etching the Al layer using hydrofluoric acid. Different Characterization techniques were employed to investigate the properties of the synthesized Ti3C2Tx. The degradation of methylene blue (MB) dye under microwave irradiation in the presence of the prepared 2D MXene was studied. It was found that the synthesized Ti3C2Tx was an excellent microwave catalyst for MB dye degradation, and results obtained were promising. Using this approach, the dye was almost wholly degraded with a degradation efficiency of 99.85 % in only 10 min without adding any oxidant. The degradation was found to follow the pseudo-first-order kinetic model, and the rate constants obtained varied from 0.10 and reached up to 0.67 min−1. The effect of pH, initial MB concentration and catalyst dosage on the MB dye degradation rate has been studied. It was found that carrying out the reaction at pH values ranging from 2 to 10 did not obviously affect its rate. On the other hand, lower initial MB dye concentrations and higher catalyst dosages significantly increased the degradation rate. The high degradation efficiency was found to be maintained for up to five successive catalytic cycles, ensuring the high stability of the synthesized 2D MXene Ti3C2Tx as a catalyst. Optimization of parameters affecting the degradation process was studied using response surface methodology (RSM). According to the Box-Behnken design, the optimal degradation efficiency (99.92 %) could be achieved by adding 21.24 mg of 2D Ti3C2Tx MXene catalyst and using an initial MB dye concentration of 53.06 ppm (mg/L) during a reaction time of 11.93 min.

Surface decoration of Nb2O5 hollow fibers by graphene oxide for enhanced photocatalytic degradation of methylene blue

AbstractThis paper describes the fabrication of ceramic Nb2O5 hollow fibers covered by a thin graphene oxide (GO) layer using the vacuum‐assisted dip‐coating process for the efficient photocatalysis degradation of methylene blue (MB) under UVC light irradiation. Pristine and GO‐coated Nb2O5 hollow fibers were evaluated for photocatalytic degradation at different initial dye concentrations and pH values. A photodegradation of 66.4% of the dye molecules was achieved using the pristine Nb2O5 hollow fibers at 57.4 ± 0.1 mg mL1, initial MB concentration of 10 mg L−1, and pH of 11. Under the same experimental conditions, the GO‐coated Nb2O5 hollow fibers degraded 100% of the MB molecules. Additionally, the GO‐coated Nb2O5 hollow fibers were successfully reused for four reaction cycles and exhibited suitable long‐term stability. Thus, the proposed ceramic Nb2O5 hollow fibers with a surface decorated by a GO layer presented suitable characteristics for use as a photocatalyst in MB degradation.

Efficient dye removal using manganese oxide-modified nanocellulosic films from sugarcane bagasse

Removing toxic dyes from industrial wastewater is crucial for environmental protection. This research introduced novel composite films of manganese oxide (MnO2)-modified nanocellulose (MCel) and unmodified nanocellulose (Cel) derived from sugarcane bagasse for dye removal. Nanocellulose was extracted from sugarcane bagasse and subsequently transformed into MCel through in-situ MnO2 synthesis. The MCel/Cel composites, with various MCel to Cel ratios, were fabricated into films and evaluated for their efficiency in removing methylene blue (MB). The films were characterized using Fourier transform infrared spectroscopy for functional group analysis, X-ray diffraction for crystallinity, X-ray photoelectron spectroscopy for chemical state analysis, field emission scanning electron microscopy-energy dispersive spectroscopy for morphology and elemental composition, and Thermogravimetric Analysis for thermal behaviors. Adsorption results showed that all MCel/Cel composite films achieved over 97 % removal of MB (initial concentration 100 mg L−1) within 24 h, with convenient adsorbent retrieval after adsorption. The adsorption process followed a pseudo-second order kinetic model and Langmuir adsorption isotherm. The optimal 95:5 MCel/Cel film exhibited a rate constant of 6.16 × 10−4 g mg−1 min−1 and the calculated adsorption capacity of 181.85 mg g−1. These results demonstrate significant potential for wastewater treatment and sustainable waste valorization by converting sugarcane bagasse cellulose into environmentally friendly adsorbents for contaminant removal.

Methylene Blue Degradation Using Non-Thermal Plasma

Methylene blue (C16H18ClN3) dye can be decomposed using non-thermal plasma. However, there is a problem in that the maintenance of electrodes and dielectrics is necessary due to the durability and heat generation problems due to the high temperatures. Therefore, in this study, a comparative experiment was performed between the flat DBD plasma module and the diffuser DBD module under the same conditions. For methylene blue decomposition, the characteristic changes in the air flow rate, ozone production rate, energy consumption rate, and decomposition rate were compared. In the experiment, 7 L water was placed in a 15 L reactor, and measurements were performed for approximately 1 h. We performed the same process by setting the initial methylene blue concentration to 143 mg/L. According to the results, the flat DBD module achieved a decomposition rate of 100% in 40 min, an energy yield of 46.7 g/kWh, and an ozone generation amount of 6.5 g/h. The diffuser DBD module achieved a decomposition rate of 90%, an energy production of 24.6 g/kWh, and an ozone generation of 1.97 g/h in 60 min.

Biosorption of methylene blue by bone meal: experimental and modeling with machine learning and full factorial design

Sorption technologies have been proposed for the treatment of water containing methylene blue (MB), a toxic and persistent pollutant. Despite its environmental risks, the role of process variables in MB removal has not been fully explored through experimental design. The objective of this study is to assess the potential of bone meal powder (BMP), an underexplored agricultural byproduct, as an affordable adsorbent for the removal of MB from water. BMP was subjected to a series of analytical characterization techniques, and its adsorption capacity was evaluated through a comprehensive factorial design, which investigated the effects of biosorbent dosage, solution pH, and initial MB concentration. The study revealed that the highest adsorption level was 14.49 mg g−1, attained under the following conditions: 1 g L−1 BMP, pH 11, and 100 mg L−1 MB. The adsorption equilibrium was reached within 60 min, with a measured capacity (qexp) of 18 mg g−1. Theoretical adsorption isotherms indicated a capacity of 63 mg g−1, which aligned well with the Langmuir model. To predict adsorption outcomes, machine learning models were applied, with multiple linear regression performing best. Optimization of decision trees and neural networks improved accuracy but risked overfitting. FT-IR, XRD, and ICP analyses indicated ion exchange as a significant mechanism of adsorption. In desorption studies, H2SO4 was the most effective agent, achieving 68.72% desorption efficiency. BMP exhibited optimal recyclability for up to four cycles before efficiency declined.

Optimization of methylene blue photodegradation by Cr-PTC[sbnd]HIna/TiO2 composite using box-behnken design application

The Cr-PTCHIna/TiO2 composite synthesized using an isonicotinic acid modulated chromium and perylene-based metal-organic framework (Cr-PTCHIna MOF) and titanium oxide (TiO2) showed promising results for the photodegradation of methylene blue. The composite was synthesized through the solvothermal method with a molar ratio of Cr and Ti of 1:1 mmol. The XRD diffraction patterns of Cr-PTCHIna/TiO2 composite showed sharp peaks at 2θ = 12°, 25°, 27°, 37°, 48°, 54°, 55°, and 62° with crystal sizes of 14.144 nm. The Cr-PTCHIna/TiO2 composite has a band gap energy of 2.02 eV and a rod-shaped morphology with a particle size of 239.16 nm. The Box-Behnken Design (BBD) demonstrated that the composite can achieve an optimum degradation efficiency of methylene blue of 88.55 % under methylene blue initial concentration of 35.7 ppm, pH 6.6, and photocatalyst mass of 0.13 % under 250-watt Mercury lamp irradiation for 2 h.

3D Printed Metal Organic Framework Hydrogel for Dye Adsorption and Gas Sensing

AbstractMetal organic frameworks (MOFs) have tunable chemical structures, orderly pore structures, and modifiable surface functional groups making them a promising material for environmental remediation. However, their rigid powder morphology poses significant challenges for customizing MOF structures with adjustable mechanical properties. Here, we synthesis the stretchable UV‐curable MOF hydrogels through high‐resolution digital light processing 3D printing, and evaluated its adsorption effect on seven common dyesand.The results showed that it had selective adsorption effect on methylene blue (MB), and the adsorption effect increased with the increase of the initial concentration of MB: its adsorption capacity on 6 mgL−1, 12 mgL−1 and 24 mgL−1 MB solution reached 13.55 mgg−1, 26.31 mgg−1 and 50.70 mgg−1 respectively. Compared to powdered MOFs, the 3D‐printed MOF (Cu‐BTC) exhibited superior adsorption for dye and radioactive pollution, with methylene blue adsorption increasing from 8.93 mgg−1 to 25.05 mgg−1 and I2 adsorption from 141.56 mgg−1 to 792.65 mgg−1. Furthermore, the 3D‐printed MOF structure proved easily cleanable with dilute HCl and reusable over five times without degradation. In addition, our study highlighted the suitability of the 3D‐printed MOF for CO2‐sensing devices, demonstrating its broad applicability in environmental remediation and sensing technology.

Novel Efficient and Eco‐Friendly Biosorbent Derived from Ditax (Detarium senegalense) Fruit Hulls for Removal of Cationic Dyes: Adsorption Modeling and Statistical Optimization

AbstractRemediation of wastewater laden with dyes using optimized and less expensive techniques remains a challenge for environmental protection. In the current research work, alkaline activation approach was employed to derive a biosorbent from ditax fruit hulls (DS‐FHB), and its sorption performance was tested on Methylene blue (MB) dye biosorption with optimizing adsorption parameters. Structural and chemical properties of DS‐FHB including crystallinity, morphology, and surface functionality were analysed using XRD, SEM, FTIR technics, and pHPZC determination. Optimization of adsorption parameters using a centered composite design (CCD) from response surface methodology led to achieving a peak dye removal rate of 98.97 %. The optimal conditions were determined as DS‐FHB mass of 0.23 g, pH 7.12, contact time 39.00 min, and initial MB concentration of 69.35 mg/L. The findings demonstrated a strong alignment with both the Langmuir isotherm and pseudo‐second order kinetic model, suggesting their appropriateness in describing the adsorption process of MB onto DS‐FHB. According to the Langmuir isotherm model, the sorption of MB dye onto DS‐FHB occurred by monolayer formation with a maximum dye sorption capacity of 96.453 mg/g. Based on the structural and physico‐chemical properties of DS‐FHB biosorbent, and its adsoption applicability evaluated in the experimental conditions, detax derived‐biosorbent can be proposed as a successful and effective low‐cost biosorbent for removing cationic dyestuffs from aqueous solutions.

High-performance removal of methylene blue dye using porous lignin extracted from sugarcane bagasse by deep eutectic solvent

This study evaluated the ability of triethyl benzyl ammonium chloride/lactic acid deep eutectic solvent extracted lignin (TEBAC/LA-DES-L) to adsorb methylene blue (MB) without additional functional group modification. The structure and morphology of TEBAC/LA-DES-L were characterized using SEM, BET, FT-IR, and TGA techniques. Various factors influencing MB adsorption, such as extraction temperature, solution pH, adsorbent dose, initial MB concentration, adsorption time, and reaction temperature, were investigated. The Redlich-Peterson isotherm displayed a good fit for the experimental data, with a maximum adsorption capacity of 85.16 mg/g. Kinetic analysis suggested that the adsorption process followed the pseudo-second-order model, with adsorption occurring in <100 min on DES-L-4 h. The mechanism of MB adsorption on DES-L-4 h was attributed to electrostatic attraction, hydrophobic interactions, and hydrogen bonding forces. Overall, DES-L-4 h demonstrated high adsorption capacity and rapid adsorption rate, making it a promising adsorbent for effectively removing cationic dyes from wastewater.

Effective removal of different dyes using run-of-mine and processed coal samples

Coal, traditionally utilised solely for combustion, is now being investigated for its potential as an adsorbent in purifying drinking water by eliminating hazardous metal ions. Limited research exists regarding its effectiveness in reducing organic dye levels. Presented here are the outcomes of an extensive investigation into various carbon samples' efficacy as adsorbents for wastewater color removal. Samples of coal sourced from Western Coalfield Limited (WCL) were meticulously processed and characterized, encompassing run-of-mine coal and acid-leached coal. A comprehensive array of techniques, including scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDX), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), and Raman spectroscopy, was employed for coal characterization. Proximate analysis and gross calorific value (GCV) were employed to assess coal's physical attributes. The adsorption behavior of methylene blue (MB) and crystal violet (CV) on coal was scrutinized, varying factors such as contact time, pH, initial MB and CV concentrations, and adsorbent doses. Optimal adsorption parameters for MB were determined as pH 2, initial concentration of 1 ppm, 0.2 g adsorbent dose, and 60 min contact time. For CV, optimal conditions were pH 8, initial concentration of 6 ppm, 0.4 g adsorbent dose, and 45 min contact time. MB adsorption kinetics favored the pseudo-second-order reaction model, with Freundlich isotherms providing a better fit than Langmuir isotherms. Conversely, CV adsorption kinetics favored the pseudo-second-order reaction model, with Langmuir isotherms exhibiting a superior fit compared to Freundlich isotherms.