Anionic Dyes Research Articles

Efficacy of activated carbon using Salvadora persica stem for remediation of potentially toxic dyes from aqueous solution.

Potentially toxic dyes are introduced mainly to rivers through industrial effluents which have a high risk to human health and aquatic life. Activated carbon (AC) from the stem of Salvadora persica was synthesised to take off toxic industrial dyes from an aqueous solution. KOH was used as the activating agent throughout the preparation process for the AC. The morphology and composition of the prepared AC were studied by various analytical methods. From the overall results, it was found that the prepared AC is highly porous and thermal stability gained around 800 ℃. At room temperature, remediation of the dyes (cationic dye, methyl red and anionic dye, methylene blue) using the adsorption method was carried out to ascertain the impact of time and the quantity of AC on methylene blue (MB) and methyl red (MR) removal. During the initial 60min, equilibrium was attained for the optimum dye concentration (200mg/L). The data for adsorption on the AC obtained at equilibrium were examined by the Langmuir and Freundlich isothermmodels. Both the isotherms accurately predicted the data, with regression values of 0.99 for MR and 0.90 for MB, respectively. The equilibrium adsorption data was also analysed by kinetic models. The adsorption data well fittedin2nd order kinetic model. The results of MB and MR adsorption from solutions have demonstrated that the stem of Salvadora persica is one of the cheap and more eco-friendly options for remediation of toxic dyes from aqueous solutions.

Metal-Free Polydiacetylene-Functionalized Polymer for Photocatalytic Anionic and Cationic Dye Degradation and CO2 Capture

Metal-Free Polydiacetylene-Functionalized Polymer for Photocatalytic Anionic and Cationic Dye Degradation and CO₂ Capture

Optimization of Batch Adsorption Study Parameters of Acid Dyes onto Spent Brewery Grains

The exploration of economical and nature friendly adsorbents for dye elimination from effluent is a promising area of research, driven by the need for sustainable and economically viable solutions. This work deals with the adsorption features of Acid Blue 25 (AB25) and Acid Green 25 (AG25) dyes from aqueous solutions using spent brewery grains (SBG). After brewing process, the obtained residue consists of spent grains. Optimum conditions for AB25 & AG25 removal were found to be at pH 2, adsorbent dosage as 0.8 and 1 g/L of solution respectively and equilibrium time was found to be 60 mins. In order to adjudicate the adsorption process, analysis was carried out with kinetic and isothermal two parameter and three parameter models. The results were discovered to fit most with the pseudo-second-order (R2 = 0.990) for the kinetics and the Langmuir isotherm (R2 = 0.993) for the adsorption isotherms. The isotherms and kinetics verified that SBG had a high value of adsorption capacity. Experiment results pointed out SBG is one of the best adsorbent that eco-friendly, economical, readily accessible, and efficient on the removal of AB25 and AG25 dyes from aqueous solution.

Design of silver-zinc-nickel spinel-ferrite mesoporous silica as a powerful and simply separable adsorbent for some textile dye removal

Silver-zinc-nickel spinel ferrite was prepared by the co-precipitation procedure with the precise composition Ag0.1Zn0.4Ni0.5Fe2O4 for bolstering pollutant removal effectiveness while upholding magnetic properties and then coated with a mesoporous silica layer. The surface characteristics and composition of Ag0.1Zn0.4Ni0.5Fe2O4@mSiO2 were confirmed using EDX, FT-IR, VSM, XRD, TEM, SEM, and BET methods. The surface modification of Ag-Zn-Ni ferrite with a silica layer improves the texture properties, where the specific surface area and average pore size of the spinel ferrite rose to 180 m2/g and 3.15 nm, respectively. The prepared spinel ferrite@mSiO2 has been utilized as an efficient adsorbent for eliminating methyl green (MG) and indigo carmine (IC) as models of cationic and anionic dyes from wastewater, respectively. Studying pH, Pzc, adsorbent dosage, dye concentration, and temperature showed that efficient removal of MG was carried out in alkaline media (pH = 12), while the acid medium (pH = 2) was effective for IC removal. Langmuir isotherm and pseudo-second-order kinetics were found to be good fits for the adsorption data. Both dyes were adsorbed in a spontaneous, endothermic process. A possible mechanism for dye removal has been proposed. The adsorbent was effectively recovered and reused.

Decolorization, degradation, and detoxification of textile dye and efficient hydrogen production by highly-stable MIL-177-LT@NiFe-LDH photoelectrocatalyst: Mechanism and economical studies

Combining organic compounds with inorganic layers leads to the development of innovative organic-inorganic hybrid materials with specific functional properties, opening up possibilities for advanced applications that go beyond current technological limits. In the present study, Ti-MOF (MIL-177-LT) was decorated with NiFe layered double hydroxide (NiFe-LDH) to fabricate a heteroatom electrocatalyst (MIL-177-LT@NiFe-LDH). The synthesized electrode included capable electron transportation, long-term stability, and high specific surface area. Photoelectrocatalytic degradation of the Azo dye (Acid Red 18) from water was studied with respect to the influence of pH, bias potential, temperature, and dye concentration. It was found that hydrogen evolution reaction (HER) has minimized overpotentials, i.e., 130 and 182 mV corresponding to the current densities of 400 and 1000 mA cm−2, respectively. High stability was also observed when a current density of 5000 mA cm−2 was applied to the modified electrode for 500 h. The layered architecture of the MIL-177-LT@NiFe-LDH composite provides high surface points for the degradation of dye molecules and water splitting for HER. The electrocatalyst showed great stability in the degradation process. The experiment was powered by solar cells, reducing the need for electricity and resulting in cost savings. Additionally, the treatment process was analyzed in terms of costs. Therefore, a promising approach is suggested in this study for developing high-performance organic-inorganic hybrid materials with exceptional electrochemical and photocatalytic properties.

Enhanced removal of methylene blue and procion deep red H-EXL dyes from aqueous environments by modified-bentonite: Isotherm, kinetic, and thermodynamic

This study aims to enhance local bentonite's effectiveness in removing methylene blue and procion deep red dyes from aqueous media through organic modification with cetyltrimethylammonium bromide surfactant. Raw and modified bentonites were analyzed using XRF, XRD, FTIR, BET/BJH, and DSC techniques. The modified bentonite showed a crystalline structure and mesoporous morphology with a heterogeneous surface. Optimal adsorption conditions for MB dye were 0.2 g adsorbent dose, 60 min contact time, 60 mg/L initial concentration, and pH 8, achieving a maximum sorption capacity of 6.418 mg/g. For PDR dye, optimal conditions were a 0.125 g adsorbent dose, 40 mg/L initial concentration, 30 min contact time, and acidic pH, with a maximum adsorption capacity of 8.503 mg/g. Isotherm analysis indicated the Langmuir model best fits the adsorption data, suggesting a mono-layer adsorption process. Kinetic investigations revealed that the adsorption follows a pseudo-second-order model, indicating a chemisorption mechanism. Thermodynamic results showed exothermic adsorption for MB and endothermic adsorption for PDR. This work highlights the potential of surfactant-modified bentonite as a cost-effective sorbent for treating polluted aqueous systems, effectively removing both cationic and anionic dyes.

Organic pollutant degradation over highly efficient Mn–Mo(O,S)2 oxysulfide photocatalyst under visible light illumination

Metal oxide semiconductor photocatalysts have received remarkable consideration as a promising technology for environmental remediation and energy conversion. Oxysulfide semiconductors have narrow band gaps which are appropriate for photocatalytic removal of toxic organic pollutants under visible light illumination. For the elimination purpose of these pollutants, Mo(O,S)2, Mn(O,S)2, and Mn–Mo(O,S)2 oxysulfide catalysts containing various Mn contents were synthesized at low temperatures via a simple method. The structural, morphological, electrochemical, compositional, and optical properties of the as-synthesized catalysts were exhaustively characterized. The photocatalytic degradation activity of the bares Mo(O,S)2, Mn(O,S)2, and other Mn–Mo(O,S)2 compositions were evaluated over different types of organic pollutants under visible light illumination. The addition of Mn in Mo(O,S)2 structure improved the photodegradation activity, and Mn–Mo(O,S)2-30 was found to be the best composition with superior photodegradation performance towards the four cationic, anionic, and neutral dyes. The degradation efficiency of 10 ppm of MB, and MO dyes reach 99.7 % and 98.6 %, within 30 and 120 min, respectively. Mn–Mo(O,S)2-30 catalyst also shows a good photodegradation performance on Rh B and NR organic pollutants. According to the recycling test, the catalyst exhibited excellent performance. The photodegradation follows pseudo-first order kinetics with a rate constant of 0.097 and 0.036 min−1 for MB and MO dyes, respectively. The trapping experiment showed that superoxide anion radicals (O2•-) and holes (h+) are the responsible active species for the degradation on MO and MB, respectively. The novelty of using Mn–Mo(O,S)2-30 for various dyes degradation lies in its remarkable catalytic properties.

New Synthetic Non-toxic Mono-azo Acid Dyes with Prominent Antibacterial Properties for Potential Application on Polyamide Fabrics

New Synthetic Non-toxic Mono-azo Acid Dyes with Prominent Antibacterial Properties for Potential Application on Polyamide Fabrics

Formulation of silver phosphate/graphene/silica nanocomposite for enhancing the photocatalytic degradation of trypan blue dye in aqueous solution

Photocatalytic degradation of several harmful organic compounds has been presented as a potential approach to detoxify water in recent decades. Trypan Blue (TB) is an acidic azo dye used to distinguish live cells from dead ones and it's classified as a carcinogenic dye. In this study, silver phosphate (Ag3PO4) nanoparticles and novel Ag3PO4/graphene/SiO2 nanocomposite have been successfully prepared via simple precipitation method. Afterward, their physical properties, chemical composition, and morphology have been characterized using SEM, EDS, TEM, SAED, BET, XRD, FTIR and UV–VIS spectroscopy. The specific surface area of Ag3PO4 and Ag3PO4/G/SiO2 nanocomposite were reported to be 1.53 and 84.97 m2/g, respectively. The band gap energy of Ag3PO4 and Ag3PO4/G/SiO2 nanocomposite was measured to be 2.4 and 2.307 eV, respectively. Photocatalytic degradation of Trypan blue (TB) was studied at different parameters such as pH, catalyst dosage, initial concentration, and contact time. The results showed that, at initial dye concentration of 20 ppm, pH = 2, and using 0.03 g of Ag3PO4/G/SiO2 as a photocatalyst, the degradation percent of TB dye in the aqueous solution was 98.7% within 10 min of light exposure. Several adsorption isotherms such as Langmuir, Freundlich, and Temkin adsorption isotherms have been tested in addition to the photocatalytic degradation kinetics. Both catalysts were found to follow the Langmuir isotherm model and pseudo-second-order kinetic model. Finally, the possible photocatalytic performance mechanism of Ag3PO4/G/SiO2 was proposed.

Exploring the novel environmentally friendly dye degradation mechanism of NiO-Polypyrrole polymer nanocomposites in degrading the organic pollutants under sunlight

<p style="text-align:justify"><span style="font-size:11pt"><span style="line-height:115%"><span style="font-family:Calibri,sans-serif"><span lang="en-AE" style="font-size:12.0pt"><span style="line-height:115%"><span style="font-family:"Times New Roman",serif">According to estimates, around 15-50% of textile dyes fail to adhere to the fabric during the dyeing process, resulting in their discharge into wastewater. This wastewater is often used for agricultural irrigation in impoverished nations which harms plant germination and development. In this study, polymer composites of Polypyrrole (PPy) and nickel oxide (NiO) nanocomposites were synthesized via the hydrothermal method with different concentrations (250 mg, 500 mg, and 75 0mg) and their composite samples were employed as catalysts to degrade the anionic-brilliant blue and the cationic-crystal violet dye under 120 mins of sunlight irradiation. The process of degrading BB and CV dyes utilising nano catalysis was analysed using a pseudo-first-order kinetics model. The findings indicate that the degradation of the anionic dye is more efficient than that of the cationic dye under exposure to sunlight. Hence, the presence of NiO NPs and the NiO-PPy nanocomposite significantly impact their photocatalytic activity in degrading BB and CV dyes, achieving an impressive efficiency of around 96.99% and 89.96% respectively. Moreover, its stability has also been studied for over five cycles.</span></span></span></span></span></span></p>

Eco-friendly sustainable adsorption dyeing of MOF-modified carboxymethyl cellulose fiber fabric using acid dyes

Eco-friendly sustainable adsorption dyeing of MOF-modified carboxymethyl cellulose fiber fabric using acid dyes

Simplified synthesis of bentonite/gelatin and bentonite/sucrose composites for efficient removal of anionic and cationic dyes

Bentonite-gelatin (BT-Ge) and bentonite-sucrose (BT-Su) composites were fabricated using a simple solution mixing method and employed as adsorbents for extracting dyes from aqueous solutions. The structural characteristics of the fabricated composite materials were elucidated using x-ray diffraction, Fourier transform infrared (FTIR) spectroscopy, and thermogravimetric analysis (TGA). The adjustable adsorption capabilities of the developed adsorbents toward methyl red (MR) and methylene blue (MB), representing anionic and cationic dyes, respectively, were examined by varying the mass ratio of bentonite to gelatin and sucrose. The impact of contact time, adsorbent dosage, and pH on the adsorption process of MR and MB onto BT-Ge and BT-Su was investigated. Kinetic data fitting indicated a good agreement with the pseudo-second-order model, with equilibrium typically achieved within 30 min, resulting in 99.69 ± 0.550, 99.56 ± 0.344, 99.90 ± 0.488% removal of MB with BT, BT-Su, and BT-Ge, respectively and 99.50 ± 0.854, 99.50 ± 0.658, and 99.57%±0.501% of MR with BT, BT-Su, and BT-Ge, respectively from the aqueous solutions. Equilibrium data were analyzed using Langmuir and Freundlich isotherm models, with the Langmuir model showing the best fit and indicating a maximum adsorption capacity of 666.66 mg g−1 of MR and 285.71 mg g−1 of MB at 25 °C. These findings underscore the remarkable efficacy of BT-Ge and BT-Su composites in eliminating dyes from wastewater, particularly colored effluents.

Selective Adsorption of Dyes and Fe3+ Sensing via Tb3+ Incorporation in an Anionic Cadmium-Organic Framework.

A three-dimensional (3D) anionic cadmium-organic framework, namely [(CH3)2NH2][Cd1.5(DMTDC)2] ⋅ 2DMA ⋅ 0.5H2O (Cd-MOF; DMA=N,N-dimethylacetamide), was successfully synthesized under solvothermal conditions by using a linear thienothiophene-containing dicarboxylate ligand, 3,4-dimethylthieno [2,3-b]-thiophene-2,5-dicar-boxylic acid (H2DMTDC). Single-crystal X-ray diffraction analysis reveals that Cd-MOF exhibits a 3D anionic framework with pcu α-Po topology, featuring rectangle and rhombus-shaped channels along b- and c- axis direction. Cd-MOF demonstrates selective adsorption of cationic dyes over anionic and neutral dyes. Additionally, Tb3+-loaded Cd-MOF serves as a fast-response fluorescence sensor for the sensitive detection of Fe3+ ions with a low limit of detection (8.90×10-7 M) through fluorescence quenching.

Aloe vera-assisted biogenic synthesis of tunable magnesium oxide nanoparticles for enhanced photocatalytic and antibacterial applications

In this study, magnesium oxide (MgO) nanoparticles (NPs) tuned via doping with transition metal ions, Co2+/Cu2+/Zn2+ have been synthesized biologically using Aloe vera leaf extract as an encapsulating agent. These pure and doped MgO NPs have been characterized by using various physico-chemical characterization techniques. X-ray diffraction (XRD) analysis confirms the formation of face-centered cubic structures of pure and doped MgO NPs with their average crystallite sizes ranging from 8.11-17.83 nm. X-ray photoelectron spectroscopic (XPS) analysis confirmed the presence of doped element in their +2 oxidation state. UV-Visible spectral analysis revealed a significant reduction in band gap energies in nano-dimensions which further gets modified upon doping (1.76 − 4.9 eV). Our findings also demonstrated the engagement of phytochemicals as capping agents in Fourier transform infrared (FTIR) examination. Scanning electron microscopic (SEM) and Transmission electron microscopic (TEM) analysis provided insights into the morphologies and particle sizes. Elemental analysis by Energy dispersive X-ray (EDX) confirms the presence of Co, Cu, and Zn elements in doped MgO NPs. The photocatalytic degradation of dyes has confirmed that Co and Cu doping substantially enhance the photocatalytic activity compared to both undoped and Zn-doped MgO NPs. Furthermore, these nanoparticles demonstrate superior efficiency in degrading the cationic dye Malachite green (MG) compared to the anionic dye Methyl orange (MO). Regarding their antibacterial properties, only Cu doping induces a notable antibacterial effect in MgO NPs, particularly against gram-positive bacteria. Additionally, these nanoparticles exhibit substantial antioxidant activities. These tailored MgO nanoparticles exhibit potential for applications in wastewater treatment.

Adsorption and transport of acid dye through polymer inclusion membrane with Aliquat 336 and TBP

Colour is typically the initial pollutant identified in wastewater. Membrane separation represents a novel approach to separation processes, with expectations of supplanting many traditional separation systems. The aim of this study is to investigate polymer inclusion membranes (PIMs) consisting of tri octyl methyl ammonium chloride as the carrier, tributylphosphate as the modifier, poly-vinyl chloride as the base polymer and 2-Nitro phenyl pentyl ether as the plasticizer for removing an acid dye (Red Erionyl A-3G) from aqueous solution. The dye adsorption on the membrane surface and its transition to the stripping phase was achieved by placing the membrane between two glass cells. Changing the stripping solution ensured both adsorption on the membrane surface and the transfer of all the dye to the stripping stage. Using a mixture of 0.8 M salicylic acid and 0.8 M NaOH, along with stirring at 1000 rpm during the stripping phase, extraction efficiency reached 98% in the feed phase and 53% in the stripping phase. When 1 M NaOH solution was employed as the stripping solution, the membrane absorbed all the dye within 10 minutes, but there was no transition to the stripping phase. The membrane has a durability of 2 days.Graphical abstract

Adsorbent based on MOF-5/cellulose aerogel composite for adsorption of organic dyes from wastewater

Industries persistently contribute to environmental pollution by releasing a multitude of harmful substances, including organic dyes, which represent a significant hazard to human health. As a result, the demand for effective adsorbents in wastewater treatment technology is steadily increasing so as to mitigate or eradicate these environmental risks. In response to this challenge, we have developed an advanced composite known as MOF-5/Cellulose aerogel, utilizing the Pampas plant as a natural material in the production of cellulose aerogel. Our investigation focused on analyzing the adsorption and flexibility characteristics of this novel composite for organic dye removal. Additionally, we conducted tests to assess the aerogel’s reusability and determined that its absorption rate remained consistent, with the adsorption capacity of the MOF-5/cellulose aerogel composite only experiencing a marginal 5% reduction. Characterization of the material was conducted through XRD analysis, revealing the cubic structure of MOF aerogel particles under scanning electron microscopy. Our study unequivocally demonstrates the superior adsorption capabilities of the MOF-5/cellulose aerogel composite, particularly evident in its efficient removal of acid blue dye, as evaluated meticulously using UV–Vis spectrophotometric techniques. Notably, our findings revealed an impressive 96% absorption rate for the anionic dye under acidic pH conditions. Furthermore, the synthesized MOF-5/cellulose aerogel composite exhibited Langmuir isotherm behavior and followed pseudo-second-order kinetics during the absorption process. With its remarkable absorption efficiency, MOF-5/cellulose aerogel composites are poised to emerge as leading adsorbents for water purification and various other applications.

Eco-Friendly Synthesis of Al2O3 Nanoparticles: Comprehensive Characterization Properties, Mechanics, and Photocatalytic Dye Adsorption Study

Metal and metal oxide nanoparticles are gaining traction in inorganic catalysis and photocatalysis, driving the development of eco-friendly methods. This study introduces an eco-friendly and cost-effective approach for synthesizing Al2O3 nanoparticles (NPs) using extracts derived from the leaves of Calligonum comosum L. The primary objective of this investigation is to assess the photocatalytic efficacy of the synthesized catalyst in addressing organic pollutants. The Al2O3 NPs exhibit a spherical morphology with crystalline arrangements, as evidenced by an average crystallite size of 25.1 nm in the XRD analysis. The band gap energy of the Al2O3 NPs is determined to be 2.86 eV. In terms of mechanical properties, the Al2O3 NPs show significant potential in enhancing both flexural and compressive properties, thereby making them a viable choice for improving the mechanical performance of composites. Notably, the Young’s modulus of the hybrid composite (comprising plant material and Al2O3 NPs) exhibits a remarkable increase of 34.4% in flexion and 78.3% in compression compared to the plant material alone. The catalytic performance of the Al2O3 NPs is evaluated using methylene blue (MB) as a cationic dye and Rose Bengal (RB) as an anionic dye. Impressively, the Al2O3 NPs demonstrate degradation efficiencies of 98.2% for MB and 90.5% for RB. The degradation processes occur under solar light irradiation, with a contact time of 120 m, a maintained pH of 7, and a temperature of 25 °C. This study found that Al2O3 nanoparticles are a promising, cost-effective, and environmentally friendly option for water treatment.

Defects-rich MgFe LDH: A high-capacity adsorbent for methyl orange wastewater

Dye pollution is a common pollutant in wastewater that poses a serious threat to human health. Layered double hydroxide (LDH) is a commonly used adsorbent for dye removal. However, its adsorption efficiency is significantly limited by the limited adsorption active sites of the adsorbent. In this paper, a defects-rich MgFe LDH adsorbent for anionic dye wastewater was synthesized by a simple hydrothermal method and alkaline etching. Different analytical techniques, such as XRD, FT-IR, SEM, TEM, XPS, and N2 adsorption-desorption isotherm, were used to verify the chemical composition and surface characteristics of the materials, and the effects of pH, temperature, and contact time on the adsorption effect of methyl orange and the adsorption mechanism were analyzed. Alkaline etching of Al and Zn in the laminate generated defects that expose unsaturated coordination centers and create abundant adsorption sites, which can electrostatically attract and coordinate with dye ions. At 25°C, the adsorption capacity of MgFe LDH with Al etched and MgFe LDH with Zn etched for methyl orange dye reached 1722 mg/g and 1685 mg/g, respectively, much higher than that of MgFe LDH (544 mg/g). This work provides a promising method for the removal of dye wastewater by adsorption and a new idea for the design and development of high-performance dye wastewater adsorbents.

Green hybrid coagulants for water treatment: An innovative approach using alum and bentonite clay combined with eco-friendly plant materials for batch and column adsorption

Textile industries contribute to water pollution through synthetic dye discharge. This study explores the use of natural bio-coagulants to remove acid dyes from wastewater, investigating factors like pH, coagulant dose, dye concentration, contact time, and temperature for optimal results. The optimum pH and coagulants capabilities of (CAAPP, CAAPH, CBAGL, CBAPP and CBAPH) were 3 (49.6 mg/g), 3 (42.5 mg/g), 3 (38.9 mg/g), 4 (35.7 mg/g), 4 (34.1 mg/g), and 4 (29.4 mg/g) respectively, while treating of selected BRF-221 dyes from water solution. The acidic range (3–4) was found to have the best pH for the maximal coagulation, and the optimal dose were found to be 0.05 g/50 mL. The equilibrium was attained within 45–60 min for all coagulants. After 60 min of shaking, the maximum coagulation capacities (21.9, 21.02, 16.5, 27.9, 25.3, and 23.4 mg/g) of several coagulant composites (CAAGL, CAAPP, CAAPH, CBAGL, CBAPP, CBAPH) were determined. The initial BRF-221 dye concentration in the range of 10–200 mg/L was considered as optimum for gaiting maximum elimination of dye using different coagulants. At a dye value of 100 mg/L of BRF-221, maximal coagulation capacities CAAGL (179.19 mg/g), CAAPP (166.06 mg/g), CAAPH (141.60 mg/g), and CBAGL (126.49 mg/g), CBAPP (113.9 mg/g), CBAPH (93.08 mg/g) were attained. The study found 35 °C to be the optimal temperature for maximum acid dye removal using bio-coagulants. Increasing temperature reduced coagulation capacity, indicating an exothermic process. Freundlich and Langmuir isotherms showed suitability for pseudo-first-order and pseudo-second-order kinetics in biosorption. Thermodynamic parameters were assessed for process feasibility. Effective coagulants demonstrated sensitivity to electrolyte variations. In column studies, adjusting parameters achieved maximum coagulation efficiency for removing BRF-221 dyes. The study successfully applied optimal parameters to remove real textile effluents at a practical scale. SEM, FT-IR, BET and XRD characterized coagulants, providing insights into stability and morphology.

Utilization of Biodegradable Nanofiltration Membrane for Efficient Removal of Anionic Textile Dye

Utilization of Biodegradable Nanofiltration Membrane for Efficient Removal of Anionic Textile Dye