Cationic Dye Research Articles

A sustainable approach for the simultaneous removal of cationic and anionic dyes from waste water using multilayer MWCNT, UMCNO, and PVA coated cotton fabrics

A sustainable approach for the simultaneous removal of cationic and anionic dyes from waste water using multilayer MWCNT, UMCNO, and PVA coated cotton fabrics

Light‐Activated Gene Expression System Using a Caging‐Group‐Free Photoactivatable Dye

AbstractOptical regulation of transcription using chemical compounds is an effective strategy to manipulate gene expression spatiotemporally. Conventional caging approaches with photoremovable protecting groups may require intense UV‐light exposure and release potentially toxic byproducts. To address these problems, here we developed a light‐mediated transcriptional regulation system by combining a caging‐group‐free photoactivatable dye PaX560 and a multidrug‐binding transcriptional regulator QacR. The cationic dye generated from PaX560 through traceless photoconversion bound QacR and reduced its repressor function, resulting in transcriptional activation. Importantly, this system allowed transcriptional activation with a large dynamic range under mild visible light exposure and simultaneous detection of the state of the photoactivated effector. This module was integrated into the T7 RNA polymerase expression system to demonstrate light‐activated transcription in vitro and in living cells.

Facile fabrication of a low-cost carboxymethyl cellulose–polyacrylamide composite for the highly efficient removal of cationic dye: optimization, kinetic and reusability

Facile fabrication of a low-cost carboxymethyl cellulose–polyacrylamide composite for the highly efficient removal of cationic dye: optimization, kinetic and reusability

In Situ Preparation of MnO2 on the Catechol/Silane-Coated Polypropylene Nonwoven Fabrics for Effective Removal of Cationic Dyes.

Previous studies have confirmed that MnOx removes heavy metal ions and organic pollutants from water with dual effects of adsorption and oxidation coupling, significantly improving the ability to remove impurities. Nanometal oxides have a highly reactive surface but tend to agglomerate during preparation and are challenging to recycle after use. A common method is to combine nano-MnO2 with Fe3O4 to prepare magnetic materials for easy recycling. Our previous research has confirmed that catechol (CA) and (3-aminopropyl) triethoxysilane (KH550) can be co-deposited on the surface of polypropylene nonwovens to form a stable CK coating under alkaline conditions. In addition, the coating has many active groups, including hydroxyl groups, amino groups, etc. This study further investigates the secondary reactivity of CK coatings. The coordination of catechol groups and metal ions was used to anchor manganese ions to the coating. Meanwhile, the hydroxyl and amino groups were used to reduce manganese ions to Mn4+ in situ to prepare PP-(CK-MnO2). We found that the sample had an excellent decolorization effect on cationic dyes but was limited to anionic dyes. The decolorization mechanism of cationic dyes was further discussed. The results showed that the decolorization of cationic dyes had a dual effect of adsorption and oxidative degradation. Under acidic conditions, its oxidation properties were enhanced. It can be used as a highly effective decolorizing agent for cationic dyes, and the decolorization behavior is consistent with the first-order kinetics. As the pH increases, its oxidation properties gradually decrease. Although the electrostatic adsorption effect was enhanced, the overall decolorization performance was significantly reduced. Recycling experiments have proved that it can maintain >90% removal rate after five cycles. This study also demonstrated that the CK coating has dopamine-like properties, which can coordinate with metal ions to prepare metal-organic hybrid materials.

Beyond the Diffusion Limit: Pre-Associated Ion-Pair Photoinitiating Systems for Radical Photopolymerization.

The pre-association mechanism of an ion-pair Type II photoinitiating system (PIS) acting in the visible range was studied. The choice of a dye as photoinitiator (crystal violet) with an excited state lifetime of 200 ps ensured the absence of dynamical quenching by the borate salts used as coinitiators. In spite of the fact that no diffusional bimolecular quenching can take place, excellent polymerization efficiency was found, underlining the high reactivity of the PIS. A saturation effect is observed when increasing the concentration of borate as a consequence of the pre-association mechanism arising from coulombic interaction between the cationic dye and the anionic coinitiator. The association equilibria of the system were described and the corresponding association constant values were calculated, allowing to quantify the pre-association efficiency. This was further successfully correlated to the observed maximal rates of polymerization. The efficiency of this super-stoichiometric sample with an excess of borate was finally compared to the stoichiometric 1:1 dye:borate ion-pair. It is shown that the pre-association mechanism could lead to much higher efficiency than the stoichiometric ion-pair.

Recycling some byproducts for fabrication of green cement with good mechanical strength and high efficiency for wastewater treatment.

This research aims to produce green cement, as an alternative to traditional cement, with outstanding performance. Five alkali-activated cement pastes were fabricated based on NaOH-activation of slag (GGBFS), bypass (B), and/or silica fume (S). Codes of five pastes are C, C-20B, C-30B, C-10B10S, and C-20B10S, as C is the control paste containing 100% slag. The compressive strength of the fabricated pastes was measured at different curing regimes: Conventional curing for 3 months and autoclave curing at 4bar/153◦C, 7bar/178◦C, and 10bar/198◦C for 4h. XRD, TGA/DTG, SEM/EDX, and BET/BJH techniques were utilized to clarify the phase development, morphological and texture features of the formed alkali-activated composite pastes. Besides, the removal capacity of some pastes for methylene blue and indigo-carmine dyes from aqueous media was evaluated. The results confirmed that C and C10B10S (80%GGBFS + 10%B + 10%S) pastes have significant mechanical properties and distinctive meso-porosity that can remove both anionic and cationic dyes.

Antioxidant and pH-dependent cationic and anionic dye degradation activities of optimum synthesized organic@inorganic Cu hybrid nanoflowers

Antioxidant and pH-dependent cationic and anionic dye degradation activities of optimum synthesized organic@inorganic Cu hybrid nanoflowers

Effect of Washing Temperature on Adsorption of Cationic Dyes by Raw Lignocellulosic Biomass

This study evaluated the potential of using raw Maclura pomifera and wild carob for the treatment of methylene blue (MB) and crystal violet (CV) as part of the search for new, abundant, and cost-effective natural materials applicable for wastewater treatment. Additionally, it explored the impact of washing water temperature on the adsorption performance of these raw organic materials. The physicochemical properties of the materials were characterized using BET, SEM/EDS, and FTIR analyses. The effects of various experimental parameters were investigated through batch adsorption experiments. The results demonstrated that the influence of washing water temperature was material-dependent. For Maclura pomifera, the maximum adsorption capacity of methylene blue and crystal violet decreased from 134.4 and 136.6 mg g−1 for MPC to 67.1 and 90.5 mg g−1 for MPH. In contrast, the adsorption capacities of wild carob biosorbents remained consistent, with the maximum amounts adsorbed for methylene blue and crystal violet by CC, CW, and CH being close, around 78.8 and 98.9 mg g−1, respectively, indicating a minimal effect of washing temperature on this material. The adsorption of both dyes onto the adsorbents was positively affected by increasing the pH, contact time, and initial dye concentration and was negatively affected by increasing adsorbent dose or ionic strength. Adsorption isotherms and kinetics were modeled using various mathematical approaches. The kinetic data were accurately described by a pseudo-second-order model, with a significant contribution from intraparticle diffusion. The Sips and Redlich–Peterson models provided the best fit for the adsorption isotherms of both dyes on the biosorbents. These findings confirm that the selected biomaterials are excellent adsorbents for the removal of cationic dyes.

Preparation and characterisation of chitosan/bacterial Escherichia coli biocomposite for malachite green dye removal: modeling and optimisation of the adsorption process

ABSTRACT Herein, a new biocomposite was obtained by loading a bacterial suspension of Escherichia coli onto a chitosan matrix to produce a unique biocomposite (chitosan – E. coli) with effective properties for biosorption of malachite green dye from water. The physicochemical characteristics of the chitosan – E. coli biocomposite were studied by employing XRD, FTIR, FESEM-EDX and pHpzc. The optimisation of biosorption conditions was achieved using a Box-Behnken Design (RSM-BBD) to assess the effect of variables on the dye removal: biocomposite dose (0.02–0.1 g/100 mL), pH (4–8) and contact time (10–300 min). The optimal conditions for dye removal (84.3%) were achieved with a chitosan – E. coli dose of 0.1 g/100 mL, and a contact time of 160 minutes with a pH of 8. The equilibrium and kinetic experimental findings show the biosorption of malachite green dye by chitosan – E. coli follows the Langmuir and pseudo-second-order models, respectively. The maximum dye adsorption capacity (q max ) of malachite green for the chitosan – E. coli biocomposite was 164.7 mg/g, where the dye adsorption mechanism was attributed to several effects such as hydrogen bonding, n-π interactions, and electrostatic attraction. Thermodynamic analysis indicated that the biosorption process was spontaneous and endothermic, with a positive enthalpy change (ΔH° = 40.9 kJ/mol) and a negative Gibbs free energy (ΔG°) at all tested temperatures. The biocomposite chitosan – E. coli adsorbent exhibits favourable cationic dye adsorption that is anticipated to have utility for remediation of dye effluent in industrial wastewater.

PVA/AMPS hydrogels: Promising adsorbents for wastewater treatment with high efficiency and reusability

AbstractA PVAMPS hydrogel was synthesized through chemical cross‐linking and semi‐interpenetration of Poly (vinyl Alcohol) (PVA) and 2‐Acrylamido‐2‐methyl‐1‐propanesulfonic acid (AMPS) with glutaraldehyde in distilled water. Various ratios of PVA/AMPS, namely PVAMPS‐1 (2:1), PVAMPS‐2 (1:1), and PVAMPS‐3 (1:2), were examined to understand their individual impacts on gel formation. The synthesis of hydrogels was confirmed using FT‐IR and solid‐state 13C NMR spectroscopy. The PVAMPS hydrogels demonstrated high efficiency as a selective adsorbent for removing cationic dyes, such as Methylene Blue, Safranine‐O, and Thionine, from aqueous solutions, with over 90% removal of cationic dyes observed within 18 hours. Regeneration and reusability studies revealed that even after four cycles, the adsorption capacity of the PVAMPS hydrogels remained exceptionally high, with removal rates exceeding 90% for Methylene Blue. However, for Safranine‐O and Thionine, the removal rates dropped to 20% and 23%, respectively, after four cycles. These findings underscore the promising potential of PVAMPS hydrogels for the removal of cationic dyes in wastewater treatment.

Influence of symmetry breaking on the absorption spectrum of crystal violet: from isolated cations at 5 K to room temperature solutions.

We report the resolution of a long-standing puzzle in molecular spectroscopy: the origin of the shoulder in the room temperature solution absorption spectrum of crystal violet (CV) - an archetypal cationic triphenylmethane dye. This was achieved by comparing experimental and theoretical results for CV in solution at room temperature and as an isolated cation in gas-phase at 5 K. The two lowest energy electronically excited states involved in the visible region absorption are degenerate and coupled via a Jahn-Teller (JT) mechanism involving phenyl torsions, making CV particularly sensitive to environmental perturbations. The shoulder is absent in the low-temperature isolated cation spectrum, and vibronic simulations based on time dependent density functional theory (TD-DFT) indicate negligible JT effects under these conditions. Combining vibronic simulations with molecular dynamics, demonstrates that in water and toluene solution at room temperature the shoulder arises mainly from an intermolecular, Jahn-Teller-like symmetry-breaking effect induced by the fluctuating electrostatic potential of the disordered solvent environment, rather than from molecular distortions.

Nanowire-like phosphorus modulated carbon-based iron nanozyme with oxidase-like activity for sensitive detection of choline and dye degradation

Choline is mainly supplemented through food intake, lack of choline would result in diseases like liver cirrhosis, hardening of the arteries, or neurodegenerative disorders. The accurate detection of choline is important for human health. Herein, a novel nanowire-like phosphorus/nitrogen co-doped carbon-based iron nanozyme (Fe-NPC) with outstanding oxidase-like activity was synthesized, and the influence of phosphorus doping on oxidase-like activity was explored. Proper phosphorus doping was found to enhance the oxidase-like activity of Fe-NPC by increasing surface defects, promoting iron loading, and modulating chemical environment of central site. The oxidase-like activity of Fe-NPC was successfully applied to colorimetric-fluorescent dual mode detection of choline, and good linear relationship in the ranges of 3–200 μM were achieved with LODs of 1.95 and 1.50 μM, respectively. The fluorescent detection was constructed based on the fluorescence quenching of silicon quantum dots (Si QDs) by quinone-imine. The quenching mechanism was attributed to FRET due to the large spectra overlap, reduced fluorescence lifetime and proper donor−acceptor distance. The successful application to the detection of choline in milk proved the practicability of the proposed sensing method. The oxidase-like properties of Fe-NPC was further used in the degradation of cationic dye methyl blue, high degradation efficiency of 74 % was achieved within 5 min under optimal conditions, proving the enormous potential of Fe-NPC for application in environment protection.

Fabrication and adsorption characteristics of cuprammonium cellulose-based membranes for removing anionic and cationic dyes

A cotton linter-based source was used to form conjugate electrospun membranes composed of cuprammonium cellulose, polyethylene oxide, and polyacrylonitrile for the removal of the anionic and cationic dyes from aqueous media. The highest removal efficiencies of 94 %, 89.9 %, 87.4 % were achieved for the anionic dyes Congo red (CR), Metanil yellow (MY), and Methyl orange (MO), respectively, and less so on the cationic dyes Crystal violet (CV), and Rhodamine B (RB) were 55.8 % and 15.1 %, respectively. The pseudo-second-order model effectively described the adsorption kinetics for both types of dyes. The composite membrane exhibited adsorption behaviors following the Dubinin-Radushkevich (D-R) isothermal model. Thermodynamics study suggests that the adsorption process was spontaneous except for the RB dye. The activation energy values of CR, MY, MO, CV, and RB dyes were 27.65, 21.17, 11.50, 10.47, and 71.12 kJ/mol, respectively, confirming the physisorption phenomenon for CR, MY, MO, and CV dyes, while chemisorption occurs for RB dyes. This study investigates the potential of a conjugate electrospun membranes as a reusable adsorbent for dye removal. The effects of solution pH, temperature, and dye concentration on adsorption performance were systematically evaluated. The conjugate electrospun membrane efficiency declined by only 10 % after undergoing five adsorption/desorption cycles.

Composite of Hydrolyzed PAN and β-Cyclodextrin Forms a Nanofiber Membrane with an Excellent Removal Effect on Various Cationic Dyes and Copper Ions.

The presence of dyes and heavy metals in wastewater represents a significant environmental and public health hazard, necessitating the development of efficient materials for their removal. In this study, we modified hydrolyzed polyacrylonitrile (PAN-H) and combined it with β-cyclodextrin (β-CD) by using an electrostatic spinning technique to fabricate composite nanofibrous membranes for water treatment applications. The resulting PAN-H/β-CD nanofiber membranes exhibit spindle-shaped fibers and porous structures with a high density of charged functional groups, which significantly enhance their selective adsorption capacity compared to pure PAN fibers. Furthermore, post-treatment with a sodium bicarbonate solution further improved this capacity, resulting in the membranes demonstrating a remarkable adsorption efficiency for cationic dyes. The adsorption process conformed to the Langmuir and pseudo-second-order kinetic models, with maximum adsorption capacities of 216.94 mg/g for methylene blue (MB), 471.59 mg/g for malachite green (MG), 299 mg/g for crystal violet (CV), and 43.95 mg/g for copper ions. The selective adsorption of these positively charged contaminants, particularly cationic dyes and metallic copper, indicates that PAN-H/β-CD membranes have significant potential for the treatment of wastewater containing similar pollutants.

Optimizing catalytic performance: Reduction of organic dyes using synthesized Fe3O4@AC magnetic nano-catalyst

This article presents a sustainable method for the catalytic reduction of both simple and binary dye systems using magnetic activated carbon (Fe3O4@AC) synthesized from almond shells, an agricultural waste biomass. The reduction of methylene blue (MB) and Congo red (CR) was investigated in the presence of NaBH4, and a series of physical-chemical experiments were conducted to elucidate the mechanism of dye conversion and its performance. The results confirmed the successful synthesis of Fe3O4 nanoparticles on the activated carbon surface. The calculated rate constants in a simple system were 0.34 min⁻1 for MB and 0.25 min⁻1 for CR, in the binary system, the Fe3O4@AC catalyst demonstrated enhanced selectivity for the cationic MB dye, attributable to the robust, attractive surface charge. The study aimed to enhance catalytic performance by employing optimization curves generated from a three-level Box-Behnken Design (BBD) simulation. Experimental results indicated that the optimal catalyst dose, dye concentration, and reaction duration were 4–7 mg, 80–120 mg/L, and 5–20 min, respectively. Response surface methodology (RSM) was developed by processing the findings from 17 replicated experiments using a two-quadratic polynomial model, establishing a functional link between the experimental parameters and MB conversion. Optimal conditions for MB conversion were determined to be 7 mg of catalyst, 80 mg/L of MB concentration, and a reaction time of 12.5 minutes, resulting in an estimated conversion rate of 99.99 %. This prediction was validated by experimental findings, with regression analysis confirming a high correlation (R2 > 0.99) between the predicted and observed values. Additionally, the Fe3O4@AC catalyst demonstrated good recyclability and stable performance over three consecutive cycles, maintaining high conversion efficiency without loss of performance. These findings demonstrate that Fe3O4@AC is a viable approach for the rapid and efficient remediation of dyes in water.

Polymeric Adsorbent for the Effective Removal of Toxic Dyes from Aqueous Solutions: Equilibrium, Kinetic, and Thermodynamic Modeling

AbstractThis study investigates the adsorption behavior of anionic (Congo red, Eosin yellow) and cationic (Malachite green) dyes on synthesized TD polymer particles, highlighting the material's potential as an effective adsorbent for industrial wastewater treatment. Key operational parameters, including initial solution's pH, contact time, initial dye concentration, and temperature, were systematically evaluated to determine their influence on adsorption efficiency. The experimental data demonstrated that the Langmuir isotherm provided the best fit for all three dyes, indicating monolayer adsorption with maximum adsorption capacities of 153.8 mg/g for Malachite green, 49.36 mg/g for Congo red, and 227.9 mg/g for Eosin yellow. Kinetic analysis revealed that the adsorption of Malachite green and Congo red followed pseudo‐second‐order kinetics, while Eosin yellow adsorption was better described by the intra‐particle diffusion model. Thermodynamic assessments, including Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°), confirmed the spontaneous and endothermic nature of the adsorption processes for Malachite green and Eosin yellow, contrasting with the exothermic behavior observed for Congo red. These findings underscore the versatility and effectiveness of TD polymer particles in removing both anionic and cationic dyes from aqueous solutions. Further research could explore material optimization and real‐world applications to broaden their utility in sustainable water treatment strategies.

Novel carboxymethyl cellulose-based hydrogel embedded with metal organic framework for efficient cationic dye removal from water

The rGO/CMC/β-CD (RCβ) hydrogel was synthesized from reduced graphene oxide (rGO), β-cyclodextrin (β-CD) and sodium carboxymethyl cellulose (CMC) by radical polymerization. A novel hydrogel adsorbent was created by growing the metal-organic framework (Cu-BTC) in-situ on RCβ hydrogel, which has excellent adsorption capacities for cationic dyes in wastewater. The adsorption parameters such as the amount of adsorbent, pH of solution and adsorption time were optimized through batch adsorption experiments. Under the optimal conditions of pH 6.0, adsorbent dosage of 0.01 g and experimental temperature of 25 °C, Langmuir isothermal model was used to fit the maximum adsorption capacities of methylene blue (MB), crystal violet (CV) and malachite green (MG), which were 892.66, 842.75 and 633.77 mg g−1, respectively. The fitting results of adsorption kinetics revealed that the pseudo-second-order model can describe the adsorption process better. Based on proposed studies, the dye molecules were adsorbed onto RCβ@Cu-BTC hydrogel mainly through electrostatic interaction, hydrogen bonding and π–π interactions. After five cycles, the adsorption efficiency of the RCβ@Cu-BTC hydrogel for MB, CV and MG can still reach 80 %, 77 % and 72 %, which shows that the adsorbent has good adsorption performance. Various adsorption experiments shows that RCβ@Cu-BTC hydrogel has great potential in treating dye wastewater.

Identification of the degree of aging and adsorption behaviors of the naturally aged microplastics

Microplastics (MPs) inevitably experienced various aging processes in nature may exhibit varied and complex interfacial interactions with adjacent species. Therefore, clarifying the possible interfacial interactions between naturally aged MPs and organic pollutants is of great significance to assess the actual behaviors of MPs in the environment. Here several plastic packaging materials after use were employed as the raw materials and representatives of naturally aged MPs, the alteration of surface characteristics, especially the degree of aging and the adsorption properties of MPs for anionic and cationic dyes were investigated. The types and the degree of aging of MPs were identified, and the variation of oxygen-containing functional groups (carbonyl, hydroxyl, and ester groups), the hydrophilicity and surface charge character were characterized. The fitting results of kinetics and isotherm models indicated that the adsorption was mainly multi-layer on heterogeneous surfaces, with hydrogen bonding, electrostatic attraction, polar interaction, and hydrophobic partitioning possibly involving. The hydrogen bond interaction was further confirmed by FTIR spectra. The increased temperature promoted the adsorption of cationic dyes on MPs, and the increased salinity of the solution enhanced the uptake of most of the tested dyes by MPs. This research deepened the understanding on the aging degree of MPs and their interfacial interactions with hydrophilic pollutants, and provided vital information for MPs as pollutant carriers.

Biochar as an Enzyme Immobilization Support and Its Application for Dye Degradation

Wastewaters generated by the textile industry often contain significant amounts of harmful (carcinogenic and mutagenic) cationic dyes, whose efficient removal is of crucial importance. This study investigates the laccase immobilization on biochar obtained from sour cherry stones (SCS-B), as a cost effective adsorbent, and evaluates its application for brilliant green (BG) degradation. The successful immobilization of laccase on biochar was achieved via adsorption and confirmed using scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and Fourier transform infrared spectroscopy (FTIR). An immobilization efficiency of 66% was achieved using 0.274 U/mL of laccase at pH 5 and a temperature of 40 °C. The adsorption kinetics of laccase followed a pseudo-second-order model, indicating that chemical adsorption plays a significant role in the immobilization process. The BG degradation by immobilized system was further optimized by evaluating effects of pH, temperature, dye concentration, and contact time. More than 92% of BG (50 mg/L) was removed within 4 h at pH 5 and temperature of 30 °C. These findings suggest that SCS-B can effectively be used as an enzyme carrier and be further utilized for the removal of emerging pollutants, positioning it as a sustainable solution for wastewater treatment.

Modified gum ghatti based hybrid hydrogel nanocomposite as adsorbent material for dye removal from wastewater

A hybrid hydrogel nanocomposite based on the polysaccharide-gum ghatti, has been made and evaluated as an adsorbent material for wastewater treatment. The nanocomposite is composed of a network of gum ghatti-graft-poly(2-acrylamido-2-methylpropane sulfonic acid) with magnetite nanoparticles embedded within. This functional material Ggh-g-PAMPS/Fe3O4 has been characterized by FTIR, TGA, SEM, EDS, XRD, BET and VSM techniques. The presence of magnetite nanoparticles imparted superparamagnetic property to the adsorbent material enabling its easy separation after use with an external magnet. The characterization data indicated mesoporous nature of the nanocomposite adsorbent with mean pore diameter of 4.9 nm. The nanoparticles imparted high surface area to the adsorbent material the value being 4.7 m2g−1 based on nitrogen adsorption experiments. The suitability of the material as an adsorbent for removal of cationic dyes from water was checked with two cationic dyes namely, rhodamine 6G and methylene blue. The maximum adsorption capacity of the nanocomposite Ggh-g-PAMPS/Fe3O4 towards rhodamine 6G and methylene blue were observed to be 403.2 and 427.8 mg g−1 respectively from their individual solutions of concentration 500 mg L−1. The pH dependence on swelling and surface charge indicated medium of pH of 7.0 as the ideal condition for effective adsorption. Freundlich isotherm model and pseudo second order kinetic model are observed to be the most befitting models to describe adsorption. Further, the thermodynamic studies revealed the adsorption to be a spontaneous and endothermic process. The desorption study portrayed the reusability of the adsorbent material. The excellent adsorption performance and magnetic nature of the developed nanocomposite suggests its potential application as an adsorbent material in wastewater treatment.