Methylene Blue Research Articles

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.

Enhancing photocatalytic water treatment efficiency via nitrogen Self-Doping and Hive-Like Structuring in isotype homojunctions of g-C3N4 generated from Thiourea-Melamine copolymerization

The combination of overpopulation and rapid industrial progress has led to a pronounced increase in water contamination. Photocatalysis emerges as a viable solution for mitigating water pollution, and graphitic carbon nitride (g-C3N4) is considered as a particularly promising photocatalyst due to its advantageous properties, such as low cost, and high chemical stability. Nonetheless, the effectiveness of g-C3N4 is often compromised by its limited surface area and substantial recombination of photogenerated charge carriers. To address these challenges, in this work, we propose a systematic approach to develop photocatalytically efficient surface structures and intimate isotype homojunctions through the copolymerization of various g-C3N4 precursors. A range of photocatalysts, each with distinctly tailored morphologies and homojunctions, was produced and their photocatalytic performance was assessed through the removal efficiencies of model pollutants, bisphenol A (BPA), and methylene blue (MB), with each at a concentration of 10 mg L-1. The enhanced photocatalytic activity observed in the optimized sample is primarily attributed to its significantly increased surface area, which is ten times greater than that of standard g-C3N4, and a marked reduction in charge recombination, which is four times lower, facilitated by the intimate homojunction. Thus, this work will open the door to the synthesis of various highly efficient photocatalysts for application in the photodegradation of diverse pollutants, consequently mitigating adverse environmental effects.

Sulfonate-Bonded Conjugated Microporous Polymer Hollowed-Out Spheres to Capture Fluoroquinolone Antibiotics and Cationic Dyes from Wastewater.

Developing adsorbent materials for the efficient removal of multiple organic pollutants in water is of importance technological significance. In the present work, a kind of conjugated microporous polymer (CMP) with a hollow sphere structure was constructed by applying SiO2 nanoparticles as a template and 1,3,5-triethynylbenzene (TEB) and 2,7-dibromocarbazole (27-DBCZ) as building blocks via the Sonogashira-Hagihara cross-coupling reaction. In order to further improve the dispersibility of the as-resulting CMPs in water, hydrophilic CMPs (H-S-CMPs) were obtained by a sulfonation modification. The adsorption performance of H-S-CMPs on dyes and antibiotics was investigated, which was based on different experimental parameters such as the initial concentration, contact time, temperature, pH, and adsorbent dose. The adsorption isotherm, kinetics, and thermodynamics were also studied, and the possible adsorption mechanism of H-S-CMPs was discussed. The experimental results illustrated that the adsorption process of H-S-CMPs on dyes and antibiotics is more consistent with the Langmuir isotherm model and the pseudo-second-order kinetic model. The maximum adsorption capacities of H-S-CMPs for rhodamine B (RhB), methylene blue (MB), ciprofloxacin, and norfloxacin were 206.2, 324.7, 222.2, and 216.9 mg/g, respectively, which were determined according to the Langmuir isothern model. In addition, the adsorption mechanism of H-S-CMPs may be attributed to the synergistic effects of hydrogen bonding, electrostatic attraction, π-π stacking, and pore filling. After 5 cycles, H-S-CMPs still maintained good stability, and their removal rate of dyes could reach more than 70%. Notably, this polymeric hollow microsphere has been less extensively investigated as an adsorbent for the removal of dyes and antibiotics. As a result, based on the designable flexibility of CMPs and the unique structure of hollow microspheres, the material holds great promise for wastewater treatment in the presence of multiple pollutants.

Two Co(II) Isostructural Bifunctional MOFs via Mixed-Ligand Strategy: Syntheses, Crystal Structure, Photocatalytic Degradation of Dyes, and Electrocatalytic Water Oxidation

The solvothermal reactions involving cobalt ions with 5-methylisophthalic acid (H2MIP) and 1,3-bis(2-methylimidazol)propane (BMIP) yielded two cobalt(II) organic frameworks: {[Co4(MIP)4(BMIP)3]·1/2DMA}n (SNUT-31) and {[Co4(MIP)4(BMIP)3]·(EtOH)2·H2O]}n (SNUT-32) where DMA represents N,N-dimethylacetamide and EtOH signifies ethyl alcohol. Single-crystal X-ray diffraction analyses reveal that SNUT-31 and SNUT-32 possess an isomorphic structure, featuring a unique 2-fold interpenetration of 3D frameworks in a parallel manner. Notably, both SNUT-31 and SNUT-32 demonstrate remarkable performance in electrocatalytic oxygen evolution reactions and exhibit exceptional photocatalytic degradation capabilities against a model comprising three distinct dyes: rhodamine B, methyl orange, and methyl blue.

Underwater superoleophobic and underoil superhydrophobic PDA/Na2SiO3/N-TiO2coated mesh for selective oil/water separation and photocatalytic degradation of methylene blue

Underwater superoleophobic and underoil superhydrophobic PDA/Na2SiO3/N-TiO2coated mesh for selective oil/water separation and photocatalytic degradation of methylene blue

Low cost fabrication of continuous flow optofluidic microreactor for efficient dye degradation using graphene QDs@MOF (Ti) photocatalyst

The optofluidic microreactor, a convergence of optics and microfluidics, offers advanced functionalities that can be pivotal in the rapid assessment of nanocatalysts for tackling environmental contamination issues. This article presents an efficient approach for degrading Methylene blue (MB) dye, commonly used in the textile industry, within a cost-effective polydimethylsiloxane (PDMS) based continuous flow optofluidic microreactor. This microreactor combines graphene quantum dots (QDs) and NH2-MIL-125 (MOF(Ti)) as a highly effective photocatalyst coating within its microchannels. By directly incorporating graphene QDs@MOF(Ti) into the microchannels, the photocatalytic medium is brought into close proximity with the flowing MB dye solutions, thereby reducing the necessary interaction time and enhancing purification efficiency. Furthermore, the findings demonstrate an impressive degradation efficiency of ∼99% for MB dye at a flow rate of 50 μL min−1 under visible light irradiation, achieved in a single pass. Additionally, the microfluidic reactor exhibits prolonged stability of the photocatalyst, enabling its reuse without significant efficiency loss. In addition, a comparative analysis highlights the advantages of microreactor-based photocatalysis over traditional methods. These advancements in the features of the graphene QDs@MOF(Ti) nanocomposite substantiate their demonstrated superiority in degradation efficiency.

Biobased amphoteric aerogel with core-shell structure for the hierarchically efficient adsorption of anionic and cationic dyes

Efficient and simultaneous removal of anionic and cationic dyes from wastewater using low-cost and environmentally-friendly adsorbent is highly required. Herein, the carboxylated cellulose (carboxyl content: 2.97 mmol/g) derived from pomelo peel was extracted by a one-step H2O2/H2SO4-mediated oxidation method. Subsequently, a novel pomelo-peel cellulose/chitosan/sodium alginate (PCS) amphoteric aerogel with a specific core-shell structure was synthesized by multiple physical cross-linking strategies. The shell layer and core layer of the optimized P3CS0.75 aerogel can selectively adsorb cationic dyes and anionic dyes, in which, the theoretical maximum adsorption capacities were 888.27 mg/g and 1816.87 mg/g towards methylene blue (MB) and Congo red (CR), respectively. Especially, the aerogel’s core/shell layer exhibited hierarchical adsorption behavior without overlapping sites even in the binary dye systems. The adsorption performance of obtained amphoteric aerogel remained effective in a wide pH range and under different practical water systems. Moreover, the removal efficiencies for MB and CR were slightly reduced from 90.76 % and 99.66 % to 88.08 % and 91.39 %, respectively, after 5 adsorption-desorption cycles, and the aerogel’s structural integrity was also maintained due to its good compressive strength (487.16 KPa). In addition, the adsorption mechanism of PCS aerogel was investigated using adsorption kinetics, isotherm, thermodynamics, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. It was proved that the adsorption process was endothermic spontaneous-monolayer adsorption driven by electrostatic attraction and hydrogen bonding. Therefore, the prepared biobased aerogel was expected to be a prospective material for removing mixed dyes from wastewater.

საქართველოსა და უცხოეთის ქვეყნების ზოგიერთი საბადოს ბენტონიტების შედარებითი ტექნოლოგიური შეფასება

An assessment of the technological characteristics of bentonites from some deposits in Georgia and foreign countries was carried out. The superiority of Georgian bentonite clays in terms of basic physical and chemical indicators is shown; of the bentonites from foreign countries, the sample from Hungary turned out to be the best. The adsorption capacity of bentonites in relation to methylene blue (MB) has been studied. It has been established that heat treatment at a temperature of 500 0C leads to a decrease in the adsorption activity of bentonites towards MB.

Macroporous material modified efficient silver molybdate composite for effective photocatalytic degradation of dyes

Macroporous banana peel biochar (BBC), silver molybdate (Ag6Mo10O33) and new composite Ag6Mo10O33@BBC were synthesized and characterized. Ag6Mo10O33@BBC was prepared using acid modulator for the first time. The photo degradation efficiency of Ag6Mo10O33@BBC in the degradation of methylene blue (MB) was found to be 95.16 %. The adsorption and degradation properties of the photo catalyst were studied using UV–visible spectroscopic analysis and band gap calculation. The photocatalytic activity favourable properties such as reduced band gap of 2.07 eV and high surface area of 7.28 m2/g of Ag6Mo10O33 was resulted upon compositing it with BBC.

Construction of (001)-TiO2/g-C3N4 heterojunction for enhanced photocatalytic degradation of methylene blue

Construction of (001)-TiO2/g-C3N4 heterojunction for enhanced photocatalytic degradation of methylene blue

Maleic Anhydride-Modified Water Hyacinth for Adsorption of Methylene Blue and Methyl Violet

Removal of toxic pollutants is of the greatest concerns facing wastewater treatment. In this study, a chemical modification method was used to prepare the maleic anhydride-modified water hyacinth (MA-EC) for the removal of methylene blue (MB) and methyl violet (MV) from water. The maleic anhydride-modified water hyacinth biosorbent was characterized and adsorption experiments were conducted. The prepared MA-EC demonstrated considerable adsorptive efficiency toward MV and MB. It was confirmed that the maximum adsorptive capacities were 1373.58 and 434.70 mg/g for MV and MB, respectively. The adsorptive data were also fitted using Langmuir and Freundlich isotherms, and the results showed that the Langmuir isotherm adsorption model could better describe the adsorptive process. Adsorption–desorption cycling experiments demonstrated that the MA-EC adsorbent had good reusability, with adsorptive capacities of 538.88 mg/g for MV and 215.56 mg/g for MB after four cycles of desorption–adsorption.

Multifunctional property of N,N-bis (carboxymethyl) glutamic acid modified biomass material: adsorption and degradation removals of cationic dyes in wastewater

As a common type of pollutants in industrial wastewater, cationic dyes have attracted great attentions. Using biodegradable N,N-di (carboxymethyl) glutamic acid (GLDA) as ligand and corn stalk (CS) as matrix, a novel and green biomass modified material GLDA-CS was successfully prepared. The multifunctional property of GLDA-CS for removing methylene blue (MB), malachite green (MG) and alkaline red 46 (R-46) from wastewater was evaluated. The dyes were removed by the electrostatic adsorption based on the cationic adsorption properties of GLDA-CS. The removal rates of MB, MG and R-46 can quickly reach 90.4%, 96.8% and 94.8% in short time. especially for MG and R-46 even only 20 min. The adsorption capacities of the dyes still remain more than 86.5% of the initial values after 5 cycles. In a heterogeneous system, the dyes were removed by Fenton-like degradation based on the metal chelating property of GLDA-CS. 100% degradation rates of the dyes can be achieved in 35 min under the acidic region. Even if at pH 7, degradation rates are 44.1%, 47.1% and 56.6% higher than those under the conventional homogeneous system, and the degradation rate remained at 83.7% after 5 cycles. Regardless of the adsorption or degradation, GLDA-CS shows strong anti-anion interference ability. The potential mechanisms of adsorption and degradation for the dyes by GLDA-CS were deduced by quantization calculation. It is concluded that the adsorption removal of the dyes by GLDA-CS follows MG > R-46 > MB, and mainly depends on the electrostatic interaction between -COOH in GLDA-CS and -N- in the dye molecules. Based on the degradation mechanism of Fenton-like reaction, the possible active sites of the dyes attacked by free radicals and their possible degradation intermediates were predicted by the calculations of Fukui function.

Preparation of Microelectrolysis Filler Using Coal Slag for the Removal of Hazardous Substances in Contaminated Water.

Presently, the utilization of gasification slag in the context of wastewater treatment is constrained. Furthermore, the presence of dye wastewater and wastewater containing hazardous metals represents a significant threat to human health. Accordingly, the present study prepared a microelectrolytic filler (MF) from gasification slag via a high-temperature roasting method and evaluated its degradation performance in water containing organic matter and harmful metal ions. The impact of varying preparation conditions, including initial solution pH and MF dose, on the degradation process was examined. The removal of methyl blue was found to be 92.21% at an initial pH of 2, a reaction time of 300 min and a dosage of 40 g L-1. The removal of Cu(II), Cd(II), and Pb(II) metal ions was 97.32, 96.58, and 99.38%, respectively, at an initial pH of 4, a reaction time of 180 min, and a dosage of 10 g L-1. Following five cycles, the MF process demonstrated continued efficacy in the removal of dyes and heavy metals from the wastewater. A mechanistic analysis revealed that the water treatment process is not a single adsorption process. Instead, it was found that organic macromolecules undergo chain-breaking reactions, while heavy metal ions undergo redox reactions. The wastewater treatment process comprises a number of distinct strategies, including electrochemical reactions, adsorption, flocculation, and precipitation. These findings illustrate the potential of a gasification slag green recycling approach to treat waste with waste, in alignment with the principles of sustainable development.

Methylene Blue and Blood Transfusion in Hemorrhagic Shock Resuscitation: An Experimental Porcine Study.

Hemorrhagic shock requires immediate treatment to prevent mortality and organ dysfunction. This study evaluates the efficacy of methylene blue (MB) with blood transfusion (BT) as a potential rescue therapy in acute severe bleeding in pigs. Thirty animals were randomly assigned to one of six groups following the induction of fixed-pressure hemorrhagic shock, after reaching a mean arterial pressure (MAP) of 55 mmHg - Group 1 (60 BT: BT after 60 minutes), Group 2 (60 MB: MB infusion after 60 minutes), Group 3 (60 MB + BT: MB and BT after 60 minutes), Group 4 (15 MB + BT: MB and BT after 15 minutes), Group 5 (15 BT + 60 MB: BT after 15 minutes and MB infusion after 60 minutes), and Group 6 (15 MB + 60 BT: MB infusion after 15 minutes and BT after 60 minutes). Hemodynamic and blood gas parameters were meticulously recorded, reversal of the shock was considered when MAP reached 90% of the baseline MAP. Except for Group 2, all groups reverted from the shock. However, groups that received MB in combination with BT, specifically Groups 3 and 4, exhibited statistically significant higher ratios of maximum MAP to baseline MAP. Using MB concomitant with BT allowed the reversal of hemorrhagic shock with higher median arterial pressure levels compared to BT alone or applying MB separately from BT. This suggests that simultaneous application of MB and BT could be a more effective strategy for reversing the effects of severe acute bleeding.

Ex situ and in situ decolorization of the textile dye methylene blue by a cheese whey-microbial fuel cell

ABSTRACT Methylene blue (MB) is a textile dye that can be fatal to aquatic life, plants, and human health when discharged into the environment without treatment. A cheese whey-microbial fuel cell (CW-MFC) is a device that generates electricity from the degradation of cheese whey by microbial activity. The microbial activity of the CW-MFC during electricity production was able to decolorize MB. In this study, 50 ppm of MB was used to evaluate the decolorization capability of bacteria of the CW-MFC. A bacterial consortium present in the bioanode of the CW-MFC showed good MB decolorization in both the ex situ and in situ operations. Ex situ operation performed outside the CW-MFC reactor showed 92.2% MB decolorization within 18 h, while the in situ operation conducted inside the CW-MFC reactor showed 97.1% MB decolorization within the same timeframe. The maximum decolorization performance was achieved at pH 4 and 37 °C. The treated MB exhibited very little or no toxicity in the germination, rooting, and shooting of Oryza sativa compared to the untreated MB. Thus, the CW-MFC can be used as a promising technique to decolorize and remove the toxic effects of MB-contaminated wastewater, and the treated wastewater can be applicable for irrigation purposes.

A study on the influence of metal Ag, Cu, and Fe doping on the morphological, structural, and photocatalytic activity of TiO2 nanostructures

Metal-doped TiO2 nanoparticles (NPs) were elaborated by a sol–gel method using n-butoxide of titanium (IV) as precursors. The resulting NPs were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Raman spectroscopy, and FTIR analysis. The SEM study shows the formation of a spheres-like structure. The EDX analysis proves the presence of Ag, Fe, and Cu on the doped TiO2 NPs. XRD and Raman spectroscopy analysis show that the doping inhibited the phase transformation and stabilized the anatase phase. The photocatalytic activity of prepared TiO2 NPs was evaluated in methylene blue (MB) photodegradation under UV irradiation. The results reveal that the doped TiO2 NPs were more efficient than undoped TiO2 NPs in the degradation of MB. The Cu-doped TiO2 NPs were found to be more efficient in this reaction with a degradation efficiency of about 92.31 % and a kinetic rate constant of about 10−2 min−1. The studies of the reactive species show that the holes are the main reactive species responsible for the photocatalytic oxidation of MB. Furthermore, the reusability studies showed that the photocatalysts are globally stable for the photodegradation of MB.

Preparation of Polyvinyl Alcohol–Chitosan Nanocellulose–Biochar Nanosilver Composite Hydrogel and Its Antibacterial Property and Dye Removal Capacity

In this research, silver-loaded biochar (C-Ag) was acquired from a waste fish scale, and nanocellulose (CNF) was prepared from the waste wheat stalk. Then C-Ag was loaded into chitosan-polyvinyl alcohol hydrogel (CTS-PVA) with CNC as a reinforcement agent, and a novel nanocomposite material was acquired, which could be efficiently applied for antibacterial and dye removal. By plate diffusion analysis, the inhibition areas of C-Ag-CTS-PVA-CNF (C/CTS/PVA/CNF) hydrogel against E. coli ATCC25922, S. aureus ATCC6538, and P. aeruginosa ATCC9027 could reach 22.5 mm, 22.0 mm, and 24.0 mm, respectively. It was found that the antibacterial rate was 100% in the water antibacterial experiment for 2 h, and the antibacterial activity was more than 90% within 35 days after preparation, and the antibacterial rate was more than 90% after repeated antibacterial tests for five times. Through swelling, water adsorption, water loss rate, and water content tests, the hydrogel manifested good moisturizing properties and could effectually block the loss of water and improve the stability of the C/CTS/PVA/CNF hydrogel. The pseudo-first-order and pseudo-second-order models were built, and the adsorption capacity of hydrogel to dye was analyzed, and the dye removal was more consistent with the pseudo-first-order kinetic model. The best removal effect for Congo red was 96.3 mg/g. The C/CTS/PVA/CNF hydrogel had a remarkable removal efficacy on Malachite green, Methyl orange, Congo red, and Methylene blue. As a result, the C/CTS/PVA/CNF hydrogels had robust antibacterial properties and reusability. In addition, the present research developed a facile strategy for effectual dyes removal from the aqueous medium.

Highly efficient Zn(O,S)/Mo(O,S)2 oxysulfide heterostructure photocatalyst for organic pollutant degradation

Environment and energy are presently some of the highest priority topics for mankind that need to be addressed. Organic pollutants are toxic and carcinogenic for human and aquatic life hence their presence in water even in low concentrations can cause serious health problems. Photodegradation of organic pollutants by utilizing oxide-based heterostructure photocatalysts is the promising approach to carry out remediation efficiently ascribed to the advanced optoelectronic and structural superiority of oxide photocatalysts. The Zn(O,S)/Mo(O,S)2 composites were synthesized via a facile solvothermal method at low temperatures. Several methods were used to characterize the composite morphology, structure, electrical conductivity, chemical composition, and optical characteristics. The heterostructured Zn(O,S)/Mo(O,S)2 oxysulfide was employed successfully in the photocatalytic degradation of organic pollutants. Among the as-prepared samples, the 30-ZnMoOS composite catalyst was found to have the highest photodegradation performance on various organic dye pollutants. The photocatalytic activity of the as-synthesized Zn(O,S)/Mo(O,S)2 samples was assessed on the photodegradation of different kinds of organic dyes under visible light irradiation. The photocatalytic degradation efficiency of 30-ZnMoOS composite over 10 ppm neutral red (NR), methylene blue (MB), rhodamine B (Rh B), and methyl orange (MO) was found to be 99.6 %, 99.9 %, 99.5 %, and 98.8 % within 40, 45, 180, and 180 min, respectively, under visible light illumination. In the present photocatalytic system, the superoxide (.O2-) anions, hydroxyl (.OH) radicals, and holes (h+) are proposed to be the direct reactive species causing the photodegradation of organic dyes.

Artificial Neural Network Modeling of the Removal of Methylene Blue Dye Using Magnetic Clays: An Environmentally Friendly Approach

In this study, the effectiveness of Fe3O4-based clay as a cost-effective material for removing methylene blue (MB) dye from aqueous solutions was evaluated. The structural properties of the clay and Fe3O4-based clay were analyzed using SEM, XRF, BET, XRD, FTIR, and TGA techniques. In this research, the effects of various aspects, such as adsorbent amount, contact time, solution pH, adsorption temperature, and initial dye concentration, on the adsorption of Fe3O4-based clay are investigated. The experiments aimed at understanding the adsorption mechanism of Fe3O4-based clay have shown that the adsorption kinetics are accurately described by the pseudo-second order kinetic model, while the equilibrium data are well represented by the Langmuir isotherm model. The maximum adsorption capacity (qm) was calculated as 52.63 mg/g at 25 °C, 53.48 mg/g at 30 °C, and 54.64 mg/g at 35 °C. All variables affecting the MB adsorption process were systematically optimized in a controlled experimental framework. The effectiveness of the artificial neural network (ANN) model was refined by modifying variables such as the quantity of neurons in the latent layer, the number of inputs, and the learning rate. The model’s accuracy was assessed using the mean absolute percentage error (MAPE) for the removal and adsorption percentage output parameters. The coefficient of determination (R2) values for the dyestuff training, validation, and test sets were found to be 99.40%, 92.25%, and 96.30%, respectively. The ANN model demonstrated a mean squared error (MSE) of 0.614565 for the training data. For the validation dataset, the model recorded MSE values of 0.99406 for the training data, 0.92255 for the validation set, and 0.96302 for the test data. In conclusion, the examined Fe3O4-based clays offer potential as effective and cost-efficient adsorbents for purifying water containing MB dye in various industrial settings.

Delamination of MXene using biomolecule: An effective strategy toward the utilization of delaminated MXene as fillers in polymer composites

AbstractWith the emergence of two‐dimensional (2D) materials analogous to graphene, transition metal carbides and carbonitrides with unique desirable characteristics known as MXenes have turned out to be a hot research topic. Recent studies increasingly focus on the structure–property relationships of MXenes and their hybrid formations with other materials. The exfoliation and delamination of MXenes using various agents is gaining attention, while their application in functional composites presents another exciting research direction. However, the exfoliation of multi‐layered MXene into few‐layered nanosheets using bio‐based agents remains underexplored. In this study, tannic acid (TA) is employed as a bio‐exfoliating agent to delaminate Ti3C2Tx MXene, while optimizing the ratio of TA to achieve efficient exfoliation and dye adsorption. The MXene/TA composites demonstrated a maximum adsorption capacity of 187.264 mg/g and a removal efficiency of 93.69% for methylene blue (MB) in water, in accordance with the Langmuir isotherm model. Furthermore, MB adsorption caused MXene to coagulate into floccules, enabling easy removal via filtration. The study highlights the trifold role of tannic acid in MXene as a delaminating, antimicrobial, and adsorption‐enhancing agent, creating a multifunctional MXene‐tannic acid system. It introduces a new class of hybrid materials with effective applications in water purification. Additionally, incorporating this hybrid material into polymers can fine‐tune their properties, leveraging the synergistic effects of the trio to develop high‐performance smart polymer composites for diverse applications.Highlights Synthesis of MXene from Ti3C2Tx Optimization of the delamination efficiency of the biomolecule tannic acid Characterization of tannic acid‐MXene delaminated composites Analysis of the antibacterial efficiency of tannic acid delaminated MXene Investigation of water purification efficiency of delaminated MXene