Adsorption Of Anionic Dyes Research Articles

Enhanced adsorption of anionic dyes onto NaOH modified green coffee waste biochar: characteristics and performance evaluation

Enhanced adsorption of anionic dyes onto NaOH modified green coffee waste biochar: characteristics and performance evaluation

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.

The feasibility of activated carbon derived from waste seaweed via molten salt activation in a eutectic mixture of ZnCl2-NaCl-KCl for adsorption of anionic dyes

The feasibility of activated carbon derived from waste seaweed via molten salt activation in a eutectic mixture of ZnCl2-NaCl-KCl for adsorption of anionic dyes

Brazilian bentonite/MgO composites for adsorption of cationic and anionic dyes.

Industrial effluents, especially those containing dyes, have become the main cause of contamination of water resources. In this context, Brazilian bentonite/MgO composites, with excellent adsorptive properties, were prepared and investigated for their effectiveness in removing cationic and anionic dyes from aqueous solutions. The new adsorbents were obtained using Brazilian bentonites and MgO using the mechanochemical method followed by heat treatment (at 700°C for 4h). Different characterization techniques were used for the chemical, mineralogical, thermal, surface, and morphological analysis of the raw clays and the composites. The experimental adsorption isotherms were quantified under different conditions of initial concentration, contact time, pH, adsorbent dosage, and temperature variation to interpret the adsorption mechanism of the crystal violet (CV) and Congo red (CR) dyes. The modeling results were obtained from the empirical Sips equation and Pseudo Second Order (PSO) kinetics, indicating that the adsorption of molecules is a heterogeneous phenomenon that occurs in a monolayer on the surface (ns > 1), with the adsorption rate determined by chemisorption. The composites showed the best removal efficiency performance compared to the raw bentonites, with an increase of 12% for the CV dye and 46% for the CR dye. In addition, the qmax values obtained were 423.02mg/g and 479.86mg/g (AM01). This research underscores the potential of Brazilian bentonite/MgO composites as a promising solution for the removal of cationic and anionic dyes from water, offering hope for future applications in the field of environmental engineering and materials science.

The potential of Gd doping as a promising approach for enhancing the adsorption properties of nickel-cobalt ferrites.

The study shows that the addition of gadolinium ions has a significant impact on the structure, morphology, and adsorption properties of Ni-Co spinel ferrite that was synthesized by the sol-gel auto-combustion method. The research also indicates that the higher the Gd content, the greater the increase in the lattice parameter, which suggests that Gd3+ ions uniformly replaced the octahedral Fe3+ ions. The morphology and chemical composition of Gd-doped Ni-Co ferrites have been studied using SEM and EDS. Gd adding to the NiCoFe matrix increases the BET surface area by 50% (from 48 to 72 m2/g) and promotes the formation of mesopores with an average radius from 3.9 to 4.9nm. The pHPZC values of Gd-doped ferrites are in the range of 7.22-7.39, which means that the ferrite surface will acquire a positive charge at natural pH, so this will promote the adsorption of Congo red anionic dye through electrostatic interaction forces. Langmuir, Freundlich, and Dubinin-Radushkevich models were used to explain the mechanism of CR adsorption on the Ni0.5Co0.5GdxFe2-xO4 adsorbent surface. The ionic-covalent parameter has been estimated to describe the surface acid-base properties. Overall, this study highlights the potential of Gd3+ doping as a promising approach for enhancing the adsorption properties of nickel-cobalt ferrites.

In Situ Growth of Nitrogen-Doped Fluorescent Carbon Dots on Sisal Fibers: Investigating Their Selective and Enhanced Adsorption Capabilities for Methyl Blue Dye.

Preparing a biomass adsorbent material with high-absorption performance but low cost plays a vital role in wastewater treatment. In this study, a novel nitrogen-doped sisal fiber-based carbon dots (SF-N-CDs) composite was prepared by directly growing carbon dots (CDs) on sisal fiber (SF) using a microwave method with polyethyleneimine (PEI) as a raw material. The prepared SF-N-CDs were characterized using FTIR, XRD, Contact angle(CA), TGA, XPS, and SEM. The results revealed that the CDs were successfully grown on SF. The adsorption properties of SF-N-CDs were significantly enhanced when they adsorbed methyl blue (MeB) dye. Specifically, the adsorption of MeB by SF-N-CDs was up to 619.7mg/g, which was about 2.6 times higher than that of raw SF. This implied that the introduction of CDs increases the adsorption site, thus enhancing the adsorption capacity. Analysis on kinetics and thermodynamics of MeB adsorption by SF-N-CDs revealed that the adsorption process followed the Langmuir isotherm model and were consistent with both kinetic models. It signifies that the adsorption involves both physical and chemical adsorption processes. Further, the SF-N-CDs maintained a removal rate of 70.9% after six adsorption-regeneration cycles, demonstrating good regeneration performance. Moreover, the SF-N-CDs could selectively separate MeB from a mixture of rhodamine B and saffron T. Consequently, the findings of this study suggest that SF-N-CDs are promising adsorbents for anionic dyes.

Green, sustainable and eco-friendly approach for extraction of silica nanoparticles from Ananas comosus and Saccharum ravannae: a comparative study of dye removal from aqueous solution

ABSTRACT Silica nanoparticles (SiNPs) were extracted in an eco-friendly manner from the crown of Ananas comosus (pineapple, AC SiNPs) and leaves of Saccharum ravannae (weed grass, SR SiNPs). Initial studies were performed to examine the adsorption of various cationic (Methylene blue, MB; Safranin, SA), anionic (Trypan Blue, TB; Eosin yellow, EY), and neutral dyes (Neutral red, NR). The investigation revealed that the maximum removal was achieved at an adsorbent dose of 1 g L−1 at an optimum pH of 7–8, at an equilibrium contact time of ∼15 mins for the dye concentration of 10 mg L−1 at 298 K. Adsorption followed the pseudo-second-order kinetic model and Freundlich isotherm model, indicating multi-layered heterogeneous adsorption. The maximum adsorption capacity (qmax) for MB, SA, and NR was found to be 81.3 mg g−1, 21.74 mg g−1, and 24.75 mg g−1 respectively, for AC SiNPs. The qmax for SR SiNPs was found to be 78.12 mg g−1, 47 mg g−1, and 70 mg g−1 for MB, SA, and NR respectively. Moreover, desorption studies showed that till 4–5 cycles, >90% of the removal efficiency was retained. Thus, the biogenic and non-toxic SiNPs can be a greener, eco-friendly alternative material for dye removal from wastewater.

Selective Adsorption of Anionic Dyes by Graphene Oxide Adsorbent

Selective Adsorption of Anionic Dyes by Graphene Oxide Adsorbent

Enhancing the valorization of pulping black liquors in production effective aerogel–carbon nanostructure as adsorbents toward cationic and ionic dyes

This work deals with promoting the efficiency of removing the cationic and ionic dyes by new aerogel–carbon nanostructures. For cleaner production the rice straw-pulping black liquors, which regards serious environmental risk during routine disposing, is used in preparing the aerogel precursors. These aerogels (AGBs) depend on using pulping black liquor in hybrid with resorcinol and the less carcinogenic formaldehyde butyraldehyde. Black liquors from five pulping processes are used, Elemental, thermogravimetric (TGA and DTG), and FTIR-ATR analyses are used to characterize the carbon precursors. While their adsorption behavior toward cationic and anionic dyes are accessed via iodine-value, adsorption capacity and kinetic models, textural characterization, and SEM. The TGA measurements reveal that AGBs from BLs of neutral sulfite and soda-borohydride pulping reagents have higher activation and degradation energies than other aerogels. In terms of cationic and anionic dyes adsorption as well as textural characterization, the AGB-CNSs surpass that made from BLs. The discarded KOH/NH4OH black liquor is used to synthesize the best aerogel precursor for producing cationic methylene blue dye (MB) adsorbent, where it provides an adsorption capacity 242.1 mg/g. The maximum anionic brilliant blue dye (BB) adsorption capacity, 162.6 mg/g, is noticed by Kraft BL-aerogel-CNSs. These finding data overcome the literature carbon adsorbents based on lignin precursors. All examined CNSs toward MB dye follow the Langmuir adsorption equilibrium; while primarily the Freundlich model for BB dye. The pseudo-second-order kinetic model well fits the adsorption kinetics of investigated AGB-CNSs. The textural characterization and SEM revealed a mixture of mesoporous and micro porous features in the CNSs.

Bio-inspired magnetic chitosan/Iron oxide macromolecules for multiple anionic dyes adsorption from aqueous media

Organic anionic dyes are major water pollutants due to their low degradability caused by complex aromatic structures. Not only do they exert toxic, mutagenic, teratogenic, tumorigenic, and genotoxic effects, but they also decrease fertility and cause irritation to the skin and respiratory system in humans. This long-term toxicity has detrimental effects on aquatic organisms and their surroundings, resulting in an imbalanced ecosystem. In this study, a Cs@Fe3O4 magnetic biosorbent was synthesised to uptake three anionic dyes and characterised for FTIR, BET/BJH, XRD, TGA, VSM, and FESEM analyses. The biosorbent average surface area was confirmed to be 52.6524 m2/g, with average pore sizes of 7.3606 nm and 6.9823 nm for adsorption-desorption processes, respectively. Batch adsorption studies pH values, contact times, temperature, initial dye concentrations, and adsorbent dosages were examined. Several isotherm and kinetic models were studied to determine the adsorption mechanism. The adsorption data of these dyes at equilibrium was observed to match Langmuir's isotherm and pseudo-second-order kinetic models. The thermodynamic study revealed that the adsorption process for these dyes was an exothermic reaction. Maximum adsorption capacities for congo red, methyl orange, and metanil yellow were 117.77 mg/g, 137.77 mg/g, and 155.57 mg/g, respectively. The reusability of recovered Cs@Fe3O4 after dye adsorption was evaluated up to five continuous adsorption-desorption cycles for its possible industrial applications.

CTAB Surfactant Promotes Rapid, Efficient, and Simultaneous Removal of Cationic and Anionic Dyes through Adsorption on Glycerol/Citrate Polyester

The discharge of dye waste by industries has caused environmental impacts on water properties, aquatic species, and human life. The production of eco-friendly materials for dye removal from wastewater has gained increasing interest, particularly through adsorption, as it is an efficient method for removing pollutants. However, the selectivity and limited adsorption capacity of materials for simultaneously adsorbing cationic and anionic dyes make it challenging to address the prevailing dye effluent issue. In this work, a poly(glycerol citrate) polyester was prepared without a solvent, using microwave heating, and was combined with cetyltrimethylammonium bromide (CTAB) to modulate the simultaneous adsorption of cationic (Rhodamine B, RB) and anionic dyes (acid blue 113, AB and acid red 27, AR). The formation of the polyester was successfully confirmed by ATR-FTIR and the thermal properties were evaluated by TGA and DCS. In the presence of CTAB 5 mM, the material removes almost 100% of the dyes, reaching the kinetics equilibrium in 30 min following the Pseudo-second order model. Additionally, dye adsorption on the polyester in the presence of CTAB was described by the Freundlich isotherm model, indicating a heterogeneous polyester surface that promotes a multi-layer adsorption driven by electrostatic interaction and hydrogen bonds. The material showed an adsorption capacity of 73.7 ± 3.2, 82.1 ± 4.4, and 21.2 ± 0.6 mg/g for RB, AB, and AR, respectively. Our results provide evidence that the poly(glycerol citrate)/CTAB has a higher potential for application in wastewater treatment to remove both anionic and cationic dyes.

Efficient adsorption of cationic and anionic dyes using hydrochar nanoparticles prepared from orange peel

Hydrochar nanoparticles biosorbent (HCNPs), derived from orange peel was prepared via an in-situ hydrothermal carbonization method. The HCNPs were tested as an effective biosorbent for removing cationic MB (methylene blue) and anionic MO (methyl orange) dyes. The prepared HCNPs was characterized using FTIR, CHN/O, SEM-EDX, UV–visible, XRD, PZC-titration, BET, and XPS. The biosorbent exhibits a good specific surface-to-volume ratio (28.23 m2/g and 0.069 cc/g, respectively) and mesopores size (2.41 nm). UV–Vis data confirm the graphitic nature of the carbon structures. XPS analysis reveals a high enrichment of multiple oxygen functionalities (including C-OH, C = O, and –COO- groups) on the surface. The optimal initial pHs are 3.0 and 5.0–8.0 for removing MO and MB, respectively. Electrostatic attraction plays a substantial role, with other hydrophobic forces in dye removal and binding. Equilibrium is attained during 60/90 min, with half-biosorption-time (tHST) for MB and MO are 4.72 and 6.71 min, respectively. The highest biosorption capacities are 203.4 mg/g for MB and 113.3 mg/g for MO, closely correlated with physiochemical characteristics. Experimental data follows Langmuir isotherm and PSO kinetic models, indicating monolayer chemisorption on a homogeneous surface. The biosorption process for both dyes is exothermic and spontaneous. HCNPs show high durability over multiple biosorption/desorption cycles using HCl and NaOH (0.1 M) for MB and MO, respectively. These findings highlight the promising potential of HCNPs as efficient biosorbents for removing both anionic and cationic dyes.

Incorporation of copper ion promoted adsorption of anionic dye (Acid Yellow 36) by acrolein-crosslinked polyethyleneimine/chitosan hydrogel: Adsorption, dynamics, and mechanisms

In this study, a novel adsorbent, A-PEI/CS-Cu2+, was developed by crosslinking polyethyleneimine/chitosan hydrogel with acrolein and loading it with copper ions. The adsorption process of A-PEI/CS-Cu2+ on the anionic dye acid yellow 36 (AY36) was investigated by kinetic, isothermal and thermodynamic modeling. It was noteworthy that A-PEI/CS-Cu2+ exhibited rapid adsorption with a 90 % removal rate achieved within just 5 min, which was much faster than the adsorption rate of A-PEI/CS without load of copper ions and showed its potential for rapid adsorption applications. The maximum adsorption capacity for AY36 could reach up to 3114 mg g−1. In addition, the high concentration of saline wastewater was found to have almost no effect on the adsorption reaction in the salt effect test experiment. In five desorption-regeneration cycle experiments, the sample exhibited good recyclability and regeneration performance. The driving force of the adsorption process mainly originated from the electrostatic interaction, hydrogen bonding, and intermolecular interaction, in which the addition of copper ions led to the enhancement of the electrostatic interaction and chelation between A-PEI/CS-Cu2+ and AY36. Overall, the findings suggest the excellent potential of A-PEI/CS-Cu2+ for rapid and efficient adsorption, as well as its suitability for practical applications in wastewater treatment.

Agricultural waste to environmental purifier: Application and mechanism of aminated pomelo peel for adsorption of anionic dyes and Cr(VI)

This study investigated the transformation of an agricultural byproduct, pomelo peel, into an environmental purifier by crosslinking assisted surface amination process and its use in wastewater treatment application. Surface morphology and textural analysis showed that the functionalized surface-amidated pomelo peel (SA-PP) attained a lamellar structure with an average pore size of 6.52 nm and a specific surface area of 7.82 m² g−1. Zeta potential measurements confirmed that SA-PP exhibits a positive surface charge within a pH range of 3–11. This surface characteristic facilitated the effective adsorption of anionic dyes by SA-PP, including amaranth red (Qe = 497.15 mg g−1), methyl orange (Qe = 247.93 mg g−1), bright blue (Qe = 231.53 mg g−1), and lemon yellow (Qe = 116.77 mg g−1), as well as heavy metal ions like hexavalent chromium (Cr(VI),Qe = 193.17 mg g−1). Further investigations on the adsorption of amaranth red and Cr(VI) indicated that SA-PP achieved equilibrium after 30 min. The process followed the pseudo-second-order and Langmuir isotherm models, indicating monolayer adsorption. The adsorption efficacy of SA-PP remained consistent across a wide range of pH levels. After five cycles, SA-PP was able to retain more than 60 % of its adsorption capacity, highlighting its potential as a sustainable, cost-effective, non-toxic, and biodegradable adsorbent for wastewater treatment applications.

Selective adsorption of anionic dyes and carbon dioxide using uncarbonized PVA aerogels incorporated with GO/PANI hybrids

Selective adsorption of anionic dyes and carbon dioxide using uncarbonized PVA aerogels incorporated with GO/PANI hybrids

C.I. Acid Black 1 transfer from dilute solution to perlite framework in organic waste management

Dyes, considered as toxic and persistent pollutants, must be removed from organic wastes prior to their composting and application in sustainable agriculture. Azo dyes, capable of altering the physicochemical properties of soil, are difficult to expel by conventional wastewater treatments. C.I. Acid Black 1 (AB 1), a sulfonated azo dye, inhibits nitrification and ammonification in the soil, lessens the nitrogen use efficacy in crop production and passes substantially unaltered through an activated sludge process. The retention of C.I. Acid Black 1 by raw and expanded perlite was investigated in order to examine the potential effectiveness of this aluminosilicate material toward organic waste cleanup. Dye adsorption proved spontaneous and endothermic in nature, increasing with temperature for both perlites. Expanded perlite having a more open structure exhibited a better performance compared to the raw material. Several of the most widely recognized two-parameter theoretical models, i.e., Langmuir, Freundlich, Temkin, Brunauer–Emmett–Teller (BET), Harkins–Jura, Halsey, Henderson, and Smith, were applied to reveal physicochemical features characterizing the adsorption. The Langmuir, Freundlich, Temkin, BET, Henderson, and Smith equations best fitted experimental data indicating that the adsorption of anionic dye on perlites is controlled by their surface, i.e., non-uniformity in structure and charge. This heterogeneity of surface is considered responsible for promoting specific dye adsorption areas creating dye “islands” with local dye supersaturations.

Fabrication of depth-controlled dimples on polymer microsphere and capturing of nano-sized objects

Polymer microspheres containing submicron-sized surface dimples were prepared through the acid-dissolving removal of silica nanoparticles as templates from the surface of core-shell microspheres, which were prepared by modified suspension polymerization of a silica nanoparticle-dispersed polymerizable monomer mixture (methyl methacrylate and divinylbenzene dispersing). We demonstrated depth control of the dimples on the surface of polymer microspheres and evaluated their capturing properties. The depth of the dimples could be facilely controlled by changing the surface polarity of silica nanoparticles (1 µm) as templates during the synthesis of the core-shell microspheres. The depth of the prepared dimples ranged from 250 to 810 nm, and the gate diameter of the dimple was related to its depth owing to the spherical shape of the template. The inner surfaces of the dimples were evaluated based on the adsorption of cationic and anionic fluorescent dyes. Confocal laser microscopy observations indicated that the inner surfaces of the dimples were densely stained with both fluorescent dyes, whereas the outer surfaces of the microspheres were not stained, suggesting that the inner surfaces of the dimples were more hydrophobic. Silica particles smaller than the gate diameter of the dimple were crammed (or jammed) into the inner space of the dimple, and the captured silica particles did not drop off even after washing with water more than five times. Because the larger silica nanoparticles could not be trapped, the dimples could selectively capture the nanosized objects in their inner space.

Remarkable Adsorption of Anionic Dye on the Supported Magnetic and Non-Magnetic Polymeric Nanocomposites Including Chitosan/Polyacrylamide and Chitosan/Polylactic Acid

Remarkable Adsorption of Anionic Dye on the Supported Magnetic and Non-Magnetic Polymeric Nanocomposites Including Chitosan/Polyacrylamide and Chitosan/Polylactic Acid

Comparative adsorption of cationic and anionic dye by using non-activated Black Plum seed biochar for aquatic phase: Isotherm, kinetic and thermodynamic studies

Industrial dye effluents play a major role in water pollution. Textile and leather industries are one of the important sectors that pollute the water by discharging many harmful cationic and anionic dyes during the dyeing process. This study aims to compare the dye removal efficiency of Black Plum seed biochar for the cationic and anionic dyes. The non-activated biochar was prepared through pyrolysis of Black Plum seed powder at 5700 C. The sample's surface chemistry was understood using various characterization techniques like Field Emission Scanning Electron Microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDS), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Raman-Spectroscopy and Zeta-potential. The experiments were successfully performed by conducting a batch adsorption study at different parameters such as pH, concentration, contact time and temperature. The coefficients of different isotherms and kinetics models were evaluated for non-linear study and the thermodynamic model was also applied. The maximum adsorption capacity was obtained as 42.39 mg/g for Crystal Violet (CV) dye and 6.22 mg/g for Eosin Blue (EB) dye by using the Langmuir isotherm model. Hence, the Black Plum seed biochar (BPSB) has superior adsorption capacity for the cationic dye CV ( removal - 98%) as compared to the anionic dye EB ( removal - 65%) at optimum parameters. Therefore, it is concluded that the BPSB is a natural toxin-free biosorbent and it can be used for the remediation of dyes from industrial wastewater.

One-step fabrication of millimeter-scale hollow vesicles with chitosan /DADMAC/ sodium alginate graft copolymer for enhanced anionic dye adsorption

Hollow vesicles are promising in water treatment due to their unique structure of the membrane and inner cavity. However, the adsorption capacity needs to be improved for targeted pollutants. Herein, millimeter-scale hollow vesicles were prepared with a one-step process of sequential stirring and grafting using chitosan, diallyldimethylammonium chloride, and sodium alginate as raw materials with the purpose of efficient removal of anionic dyes from wastewater. The composite vesicles were characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. The hollow vesicles showed the structure of the cationic membrane and the inner cavity, facilitating the dye adsorption. The adsorption capacity for the anionic dye Reactive Black 5 reached 698.1 mg/g, more than twice that of the binary composite vesicles without graft. The adsorption kinetics and isotherm data coincided with the pseudo-second-order and Langmuir models, respectively, and the adsorption mechanism was monolayer chemisorption. Moreover, the vesicles worked well in wide ranges of environment pH, temperature, and co-existing pollutants. They also possessed excellent cyclic regeneration performance, in which 93 % of the initial adsorption capacity was maintained after four cycles. These results indicate that the millimeter-scale hollow vesicles exhibit broad application prospects for wastewater purification.