Search

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 show that RCβ@Cu-BTC hydrogel has great potential in treating dye wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The adsorptive potential of starch nanocrystals (SNCs) was evaluated for the elimination of methylene blue (MB), crystal violet (CV), and malachite green (MG) from aqueous media in single, binary, and ternary dye systems using batch mode experiments. SNCs were extracted using mild acid hydrolysis to remove the amorphous parts of native granular starch, and they were characterized using different physicochemical methods, such as FESEM, XRD, FTIR, BET, TGA, and pH ZPC . The results revealed that the optimal pH for dye removal in both single and mixed dye systems was found to be 9.0. The equilibrium time increased from 5 to 20 min when the system was changed from single to binary, and then further increased to 30 min when the system was changed to ternary. The equilibrium data for single-dye systems exhibited a good fit with the Langmuir isotherm model (R 2  > 0.98, SEE <3.52 mg g -1 ), whereas for binary and ternary dye mixtures, the extended Langmuir model provided an accurate representation of the experimental data (R2 > 0.99, SEE <1.33 mg g -1 ). Among the single, binary, and ternary systems, the highest adsorption capacities were observed for MB, MB in the (MB + MG) binary system, and MB in the (MB + CV + MG) ternary system. The respective adsorption capacities were recorded as 79.55 mg g -1 , 61.91 mg g -1 , and 43.59 mg g -1 . The adsorption of dyes onto the SNCs was inherently spontaneous and endothermic, and adhered to the pseudo-second-order kinetic model in single dye systems as well as mixed dye systems. It can be concluded that the SNCs are capable of being utilized for five consecutive cycles in the adsorption-desorption process for single dye systems and three consecutive cycles for mixed dye systems. This suggests that the SNCs have potential as a sustainable and efficient option for dye removal in mixture systems., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In this paper, a natural Moroccan material from the Nador area in the north east of Morocco was studied as an adsorbent to remove methyl violet 2B dye from aqueous solutions. This material has never been studied before in this region, and it will be used in its raw state. It was collected and characterized by X-ray diffraction, FTIR spectroscopy, scanning electron microscopy, X-ray fluorescence, thermal analysis, N 2 gas adsorption-desorption, pH PZC , and Brunauer-Emmett-Teller (BET). The studies are realized with a 500-µm grain size and 182m 2 /g BET surface area. XRD showed the presence of significant peaks belonging to natural zeolite type clinoptilolite-Ca and minor phases. Several parameters were studied such as contact time, adsorbent mass, initial dye concentration, initial pH solution, the particle size of the material, and temperature. Out of the three isotherm models investigated after 60 min of contact time in the experiments, the Langmuir model gave the best fit to the experimental data (R 2  = 0.99). The results of kinetic and thermodynamic studies revealed that the adsorption process obeyed pseudo-second-order, spontaneous (ΔG° < 0), endothermic (ΔS° > 0). The adsorption of methyl violet 2B dye is chemisorptions and physisorption. The maximum theoretical adsorption capacity was 30.30 mg·g -1 at 23 °C for a particle diameter of 500 µm. The desorption study shows that the material can be desorbed using solvents. The reuse study indicates that the same amount of natural zeolite can be used several times which makes the process efficient and sustainable. The obtained results indicate that the country of Morocco has natural zeolite among its resources and that it can be used as an efficient adsorbent for the removal of dyes., Competing Interests: Declarations. Ethical approval: Not applicable. Consent to participate: Not applicable. Consent to publish: Not applicable. Competing interests: The authors declare no competing interests., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this work, polyvinylidene fluoride (PVDF) intercalated CuFe layered double hydroxides (LDH) membranes were fabricated and investigated for UV-LED/persulfate degradation of methylene blue (MB), crystal violet (CV), methyl orange (MO), and Eriochrome black T (EBT) dyes from water. The PVDF-CuFe membrane exhibited improved heterogeneity, surface functionality (CuO, Fe-O, Cu-O-Fe), surface roughness, and hydrophilicity. The process parameters were optimized by response surface methodology, and maximum MB removal (100%) was achieved within 45.22-178.5 min at MB concentration (29.45-101.93 mg/L), PP concentration (0.5-2.41 g/L) and catalyst dosage (1.84-1.95 g/L). The degradation kinetics was well described by a pseudo-first-order model (R 2  = 0.982) and fast reaction rate (0.029-0.089/min). The MB dye degradation mechanism is associated with HO·/SO 4 •- reactive species generated by Fe 3+ /Fe 2+ or Cu 2+ /Cu + in PVDF-CuFe membrane and PP dissociation. The PVDF-CuFe membrane demonstrated excellent recyclability performance with a 12% reduction after five consecutive cycles. The catalytic membrane showed excellent photocatalytic degradation of crystal violet (100%), methyl orange (79%), and Eriochrome black T (60%). The results showed that UV-LED/persulfate-assisted PVDF-CuFe membranes can be used as a recyclable catalyst for the effective degradation of dye-contaminated water streams., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

In this research, aluminum metal-organic framework encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge (Al-MOF@PIC) was prepared. SEM, FTIR, XPS, XRD, and BET techniques were employed to thoroughly characterize the synthesized material and establish its structure and characteristics. The study discovered that the Al-MOF@PIC is an efficient way to remove dyes, which constitute a significant number of contaminants in industrial wastewater. Subsequently the adsorption of methyl violet 2B (MV-2B) dye, the surface area, pore size, and pore volume of the adsorbent decreased from 1860.68 m 2 /g, 1.62 nm, and 1.52 cc/g to 1426.45 m 2 /g, 1.11 nm, and 0.92 cc/g, individually. This modification suggested that a portion of the MV-2B dye had been removed by adsorption over the adsorbent's pores. The excellent adsorption capacity of the material was further confirmed by batch adsorption tests, which displayed a maximum adsorption capability of 646.76 mg/g for the elimination of MV-2B dye. The high adsorption energy of 26.8 kJ/mol designates that chemisorption is primarily responsible for MV-2B dye adsorption against the sponge adsorbent. The Al-MOF@PIC composite sponge demonstrated exceptional reusability over six cycles, demonstrating its strength and durability. The Al-MOF@PIC composite sponge successfully removes MV-2B from water by pore filling, π-π stacking, hydrogen bonding, and electrostatic interactions, which are the key mechanisms behind the adsorption of the dye pollutant. Its potential for practical applications is further demonstrated using Box Behnken-design (BBD) to optimize the adsorption consequences., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In today's world, major pollutants, such as cationic dyes and heavy metals, pose a serious threat to human health and the environment. In this study, a novel adsorbent was created through the electrospinning of polyvinyl alcohol/polyacrylic acid (PVA/PAA), incorporated with hexagonal boron nitride (hBN) coated with polydopamine (PDA). The integration of hBN and PDA substantially enhanced the adsorption capacity of the PVA/PAA fibers, making them highly effective in adsorbing cationic dyes such as methylene blue and crystal violet, as well as cobalt (II) ions, from contaminated water. The adsorbents were assessed to understand how their adsorption behavior varies with pH, as well as to examine their adsorption kinetics and isotherms. The results indicate that the PVA/PAA-hBN@PDA adsorbent has maximum adsorption capacities of 1029.57 mg/g, 793.65 mg/g, and 62.46 mg/g for methylene blue, crystal violet, and cobalt (II) ions, respectively. This underscores the superior performance of the PVA/PAA-hBN@PDA adsorbent when compared to both the PVA/PAA and PVA/PAA-hBN adsorbents. The adsorption kinetics adhered to a pseudo-second-order model, indicating chemisorption, whereas the Langmuir model implied a monolayer adsorption. Overall, the findings of this study highlight the efficacy of harnessing the synergistic capabilities of hBN and PDA within the PVA/PAA-hBN@PDA adsorbents, providing an efficient and eco-friendly approach to removing cationic dyes and heavy metals from contaminated water, and thereby contributing to a cleaner and safer environment for all., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Mitacs Canada. Nahid Azizi, Reza Eslami reports financial support was provided by Sensofine Inc. Hadis Zarrin reports financial support was provided by Natural Sciences and Engineering Research Council of Canada. Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Toronto Metropolitan University Faculty of Engineering & Architectural Science. Nahid Azizi, Shaghayegh Goudarzi, Reza Eslami reports financial support was provided by Toronto Metropolitan University. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Jatobá-do-cerrado fruit shells, archetypical of lignocellulosic-based biomass, were used as an adsorbent to remove crystal violet (CV) and methylene blue (MB) from water. The adsorbent was characterized using various techniques, and kinetic studies showed dye adsorption followed second-order kinetics. An experimental design investigated the effects of pH and temperature on removal efficiency, with a quadratic model fitting the data best. The results suggest pH influences MB's adsorption capacity more than temperature and at 25 °C and pH 8, MB had a desirability value of 0.89, with 95 % removal efficiency. For CV, temperature had a greater influence, with a desirability value of 0.874 at 25 °C and pH 10, and 95 % removal efficiency. Adsorption isotherm studies revealed maximum adsorption capacities of 123.0 mg·g -1 and 113.0 mg·g -1 for CV and MB, respectively. Experimental thermodynamic parameters indicated an endothermic and spontaneous process which it was supported by quantum chemistry calculations. The protocols developed confirmed the potential for adsorbing CV and MB dyes in water, achieving over 73.1 and 74.4 mg g -1 dyes removal., Competing Interests: Declaration of competing interest Authors declare they have no financial interests., (Copyright © 2024 Elsevier B.V. All rights reserved.)

This study investigates the potential of using Ficus religiosa inflorescence (peepal tree) as an efficient solution for removing crystal violet from simulated and industrial wastewater. Various analyses were conducted to understand the adsorbent's structure, including particle morphology, BET surface area, FTIR, and pH ZPC . The adsorption process was studied under different physicochemical factors such as temperature, concentration, contact time, and pH. Results revealed rapid adsorption, with 94.15% removal efficiency within the first 15 min at neutral pH. The highest observed adsorption capacity was 198.03 mg g -1 , following pseudo-second-order kinetics (R 2  = 0.99), indicating chemisorption. The Langmuir model accurately described the adsorption pathway (R 2  = 0.99), showing monolayer adsorption. Thermodynamic analysis indicated an exothermic, feasible, and spontaneous process with increased entropy. The adsorbent could be easily regenerated using a 1:1 MeOH/H 2 O mixture for up to three cycles, yielding up to 73.86%. Real-time application with industrial effluent containing crystal violet showed up to 44.70% adsorption. The experiments demonstrated reliability with evaluated standard deviations (0.017935-0.000577) and relative standard deviations (0.439-0.673%), confirming statistical reliability. In conclusion, it presents a sustainable and eco-friendly approach for removing crystal violet dye from diverse wastewater sources., (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

To effectively remove Diazinon (DZ), Amoxicillin (AMX), and Crystal Violet (CV) from aquatic environments, a novel granular activated carbon (GAC) modified with Polyethylene glycol 600 (PEG) was created and manufactured. The chemical properties were investigated using a variety of characteristic analyses, including FT-IR, XRD, FESEM, and N2 adsorption/desorption. The effectiveness of GAC-PEG's adsorption for the removal of DZ, AMX, and CV was assessed under a variety of conditions, including a pH of 4-9 for the solution, 0.003-0.05 g doses of adsorbent, 50-400 ppm starting concentration, and a reaction time of 5-25 min. For DZ, AMX, and CV adsorption, the maximum adsorption capacity (Qmax) was 1163.933, 1163.100, and 1150.300 mg g-1, respectively. The Langmuir isotherm described all of the data from these adsorption experiments, and the pseudo-second-order well explains all-adsorption kinetics. Most contacts between molecules, electrostatic interactions, π-π interactions, hydrogen bonding, and entrapment in the modified CAG network were used to carry out the DZ, AMX, and CV adsorption on the GAC-PEG. The retrievability of the prepared adsorbent was successfully investigated in studies up to two cycles without loss of adsorption efficiency, and it was shown that it can be efficiently separated., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Choopani et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

In the study, a novel chitosan biopolymer and 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid (IL)-incorporated sulfonated poly (ether ether ketone) (SPEEK) composite (Ch-IL@SPEEK) was prepared for adsorption of cationic crystal violet (CV) dye. The proposed composite was well characterized by several techniques. CV adsorption performance was examined via batch studies by varying various variables involving adsorbent dosage, contact time pH and temperature. The isotherm results were demonstrated the adsorption characters of the processes were Langmuirian. The maximum adsorption capacity was determined as 77.66 mg g -1 for the composite which was significantly higher than SPEEK (q max  = 45.36 mg g -1 ). The determined equilibrium time of the operated system was 360 min and the kinetic model was assessed as Elovich. At low pHs the protonated surface groups repelled the positively charged CV and the adsorption rate increased with increasing pH. The process is spontaneous and favorable as it proceeds via endothermic interactions. Furthermore, even at the end of 5 successful adsorption cycles, 77.86 % CV removal was obtained. Remarkable efficiencies were also achieved in the removal performance of different organic pollutants. Based on the reported results, Ch-IL@SPEEK composite were exhibited as an impressive adsorbent material for adsorption processes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Ionizing radiation (mainly including gamma ray and electron beam) technology provides a more efficient and ecological option for dye-containing wastewater treatment, which is supported by its successful achievements in industrial-scale applications. However, the degradation pathway of triphenylmethane dyes by radiation technology is still unclear. In this study, crystal violet (CV) was selected as representative cationic triphenylmethane dye, the decolorization and degradation performance by electron beam radiation technology was systematically evaluated. The results showed that CV can be efficiently decolorized and mineralized by radiation, and its degradation kinetics followed the first-order kinetic model. The effect of inorganic anions and chelating agents commonly existed in dye-containing wastewater on CV decolorization and total organic carbon (TOC) removal was explored. Quenching experiments, density functional theory (DFT) calculation and high performance liquid chromatography mass spectrometry (HPLC-MS) analysis were employed to reveal CV decolorization and degradation mechanism and pathway, which mainly included N-demethylation, triphenylmethane chromophore cleavage, ring-opening of aromatic products and further oxidation to carboxylic acid, and mineralization to CO 2 and H 2 O. Additionally, electron beam radiation/PMS process was explored to decrease the absorbed dose required for decolorization and degradation, and the synergetic effect of radiation with PMS was elucidated. More importantly, the findings of this study would provide the support for treating actual dyeing wastewater by electron beam radiation technology., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

In this work, an agar-graphene oxide hydrogel was prepared to adsorb Cd (II) and Methyl Violet (MV) from water. The hydrogel was synthesised and characterised through SEM and EDS. Kinetic, equilibrium and regeneration studies were carried out, in which Langmuir, Freundlich and Sips isotherm models were fitted to the equilibrium experimental data; and regarding the kinetics, studies were conducted by modelling experimental data considering both empirical and phenomenological models. SEM and EDS have shown the composite present a 3D-disordered porous microstructure and that it is mainly constituted of C and O. Sips model fitted well to Cd (II) (R 2  = 0.968 and χ 2  =  0.176) and MV (R 2  = 0.993 and χ 2  =  0.783). The q max values for MV and Cd (II) were 76.65 and 11.70 mg.g -1 , respectively. Pseudo-order models satisfactorily described Cd (II) and MV adsorption kinetics with R 2  > 0.90. Regeneration experiments revealed an outstanding reuse capacity of the adsorbent after three cycles of adsorption-desorption for both Cd (II) and MV. This study evidences the possibility of a feasible adsorbent for Cd (II) and MV removal from water for successive cycles of use.

Nanomaterials are widely employed in wastewater treatment, among which nanoferrites and their composites hold significant prominence. This study adopts a green approach to synthesize zinc ferrite nanoparticles, subsequently integrating them with polyaniline (PANI) to fabricate the ZnFe 2 O 4 -PANI nanocomposite. Characterization of the prepared ZnFe 2 O 4 -PANI nanocomposite was conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopic (SEM) techniques. Using Scherrer's equation, the crystallite size of the synthesized zinc ferrite nanoparticles was found to be 17.67 nm. SEM micrographs of the ZnFe 2 O 4 -PANI nanocomposite revealed that in situ polymerization of ZnFe 2 O 4 with polyaniline transforms the amorphous surface morphology of the polymer into a homogeneous nanoparticle structure. The adsorption of crystal violet (CV) dye onto the surface of the ZnFe 2 O 4 -PANI nanocomposite depends on pH, adsorbent dosage, temperature, concentration levels and duration. The Langmuir adsorption model fitted the data well, indicating adherence to a pseudo-second-order kinetic pattern. Thermodynamic values ΔG°, ΔH° and ΔS° indicated that the adsorption process occurred spontaneously. Advantages and disadvantages of the technique have also been highlighted. Mechanism of adsorption is discussed. From the obtained results, it is evident that the ZnFe 2 O 4 -PANI nanocomposite holds promise as a sorbent for the removal of dye from wastewater., (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

The indirect emission had a negative influence on the ecosystem of enormous amounts of harmful dyes into water. Fe 3 O 4 @Ag-MOF was successfully fabricated to capture Gentine violet (GV)) as a model example of cationic dye from their aqueous solutions was evaluated in this search as a method to eliminate dyes from water contaminants. FTIR, XPS, BET, TGA, SEM, TEM, and XRD have all been used to study this adsorbent in order to determine its structural and chemical characteristics as well as to interpret its binding mechanisms. According to the results of the characterization, the synthesized composite had a size about 45 nm, a surface area of 856.06 m 2 /g, and considerable magnetic characteristics (66.2 emug -1 ). Consequently, we created mesoporous surfaces that had a strong ability to interface and absorb GV dye. It is possible to use the pseudo-second order rate equation to characterize the kinetic profile., while the Langmuir equation fits isotherm models. At pH 9, maximum sorption capacities can reach 1.68 mmol.g -1 . Additionally, the investigations of temperature profiles indicated the endothermic process and Thermodynamic parameters were discovered as, ΔG°, ΔH° and ΔS° The synthesized adsorbent had an interestingly high reusability of > 92 percent up to the sixth cycle. These findings revealed that a mixture of electrostatic interactions, π-π stacking, hydrogen bonds, and pore filling were involved in the GV adsorption mechanism. Fe 3 O 4 @Ag-MOF was successful in demonstrating its effectiveness as a point-of-use colour collection candidate from actual dyeing effluents.

In the presented study, a novel polypyrrole-decorated bentonite magnetic nanocomposite (MBnPPy) was synthesized for efficient removal of both anionic methyl orange (MO) and cationic crystal violet (CV) dyes from contaminated water. The synthesis of this novel adsorbent involved a two-step process: the magnetization of bentonite followed by its modification through in-situ chemical polymerization. The adsorbent was characterized by SEM/EDX, TEM/SAED, BET, TGA/DTA-DTG, FTIR, VSM, and XRD studies. The investigation of the adsorption properties of MBnPPy was focused on optimizing various parameters, such as dye concentration, medium pH, dosage, contact time, and temperature. The optimal conditions were established as follows: dye concentration of C o (CV/MO) at 100 mg/L, MBnPPy dosage at 2.0 g/L, equilibrium time set at 105 min for MO and 120 min for CV, medium pH adjusted to 5.0 for MO dye and 8.0 for CV dye, and a constant temperature of 303.15 K. The different kinetic and isotherm models were applied to fit the experimental results, and it was observed that the Pseudo-2 nd -order kinetics and Langmuir adsorption isotherm were the best-fitted models. The maximal monolayer adsorption capacities of the adsorbent were found to be 78.74 mg/g and 98.04 mg/g (at 303.15 K) for CV and MO, respectively. The adsorption process for both dyes was exothermic and spontaneous. Furthermore, a reasonably good regeneration ability of MBnPPy (>83.45%/82.65% for CV/MO) was noted for up to 5 adsorption-desorption cycles with little degradation. The advantages of facile synthesis, cost-effectiveness, non-toxicity, strong adsorption capabilities for both anionic and cationic dyes, and easy separability with an external magnetic field make MBnPPy novel., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Taking the thiazide cationic dye methylene blue (MB), triphenylmethane cationic dye crystal violet (CV), monoazo cationic dye cationic red 46 (R-46), and polycarboxycyanine cationic dye cationic rosé FG (P-FG) as the research objects, the adsorption behaviors of a self-made corn straw modified adsorbent HQ-DTPA-I for the dyes were investigated in depth. Under optimized conditions, HQ-DTPA-I can quickly adsorb most dyes within 3 min and reach equilibrium adsorption in 15-20 min. The removal rates of HQ-DTPA-I to MB, CV, R-46 and AP-FG can reach 95.28 %, 99.78 %, 99.28 % and 98.53 %, respectively. It also has good anti-interference ability for common ions present in most actual dye wastewater. For six consecutive adsorption-desorption cycles, the adsorption performance of HQ-DTPA-I can still reach 80.17 %, 81.61 %, 90.77 % and 83.48 % of the initial adsorption capacity, indicating good recovery performance. Based on Gaussian density functional theory to calculate its surface potential energy, it is found that the adsorption mechanism of HQ-DTPA-I for the cationic dyes is mainly due to the electrostatic interaction between the carboxyl groups in ligand DTPA and amino groups in dye molecules., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In present study, eco-friendly sulfated cellulose-magnetic biocomposite was successfully synthesized with a simple method from hemp biomass. ATR-FTIR was used to determine chemical changes, while FE-SEM-EDS, STEM, XRD, TG/DTA, and BET techniques were employed to identify changes in morphology, elemental composition, crystal structure, and thermal degradation. Moreover, the saturation magnetization and pHpzc values of the MSHB were also determined. The effectiveness of magnetic sulfated hemp biomass (MSHB) was tested in the removal of cationic dyes from wastewater, including methylene blue (MB), crystal violet (CV), and malachite green oxalate (MGO). The adsorption all three dyes to MSHB, the pseudo-second-order kinetic model and the Langmuir model were determined to be more appropriate, and was endothermic and spontaneous from thermodynamic parameters, too. The maximum MSHB adsorption capacities were found to be 457.6, 509.3, and 1300 mg/g for MB, CV, and MGO at 298 K. With increasing temperature, it also drastically increased in capacity. The outstanding property of the MSHB is that it shows high removal performance wide pH range, even after ten cycles its high removal efficiency is still over 96 % for all three dyes and almost unaffected from dense matrix medium. These results demonstrate that MSHB is remarkable adsorbent for removing cationic dyes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

A major worldwide challenge that presents significant economic, environmental, and social concerns is the rising generation of food waste. The current work used chicken bones (CB) and rice (R) food waste as alternate precursors for the production of activated carbon (CBRAC) by microwave radiation-assisted ZnCl 2 activation. The adsorption characteristics of CBRAC were investigated in depth by removing an organic dye (crystal violet, CV) from an aquatic environment. To establish ideal conditions from the significant adsorption factors (A: CBRAC dosage (0.02-0.12 g/100 mL); B: pH (4-10); and C: duration (30-420), a numerical desirability function of Box-Behnken design (BBD) was utilized. The highest CV decolorization by CBRAC was reported to be 90.06% when the following conditions were met: dose = 0.118 g/100 mL, pH = 9.0, and time = 408 min. Adsorption kinetics revealed that the pseudo-first order (PFO) model best matches the data, whereas the Langmuir model was characterized by equilibrium adsorption, where the adsorption capacity of CBRAC for CV dye was calculated to be 57.9 mg/g. CV adsorption is accomplished by several processes, including electrostatic forces, pore diffusion, π-π stacking, and H-bonding. This study demonstrates the use of CB and R as biomass precursors for the efficient creation of CBRAC and their use in wastewater treatment, resulting in a greener environment.

This work aims to apply the use of food-grade algae (FGA) composited with chitosan-benzaldehyde Schiff base biopolymer (CHA-BD) as a new adsorbent (CHA-BA/FGA) for methyl violet 2B (MV 2B) dye removal from aqueous solutions. The effect of three processing variables, including CHA-BA/FGA dosage (0.02-0.1 g/100 mL), pH solution (4-10), and contact duration (10-120 min) on the removal of MV 2B was investigated using the Box-Behnken design (BBD) model. Kinetic and equilibrium dye adsorption profiles reveal that the uptake of MV 2B dye by CHA-BA/FGA is described by the pseudo-second kinetics and the Langmuir models. The thermodynamics of the adsorption process (ΔG°, ΔH°, and ΔS°) reveal spontaneous and favorable adsorption parameters of MV 2B dye onto the CHA-BA/FGA biocomposite at ambient conditions. The CHA-BA/FGA exhibited the maximum ability to absorb MV 2B of 126.51 mg/g (operating conditions: CHA-BA/FGA dose = 0.09 g/100 mL, solution pH = 8.68, and temperature = 25 °C). Various interactions, including H-bonding, electrostatic forces, π-π stacking, and n-π stacking provide an account of the hypothesized mechanism of MV 2B adsorption onto the surface of CHA-BA/FGA. This research reveals that CHA-BA/FGA with its unique biocomposite structure and favorable adsorption properties can be used to remove harmful cationic dyes from wastewater.

Water pollution caused by dyes is a pressing environmental challenge due to their persistence and difficulty in degradation. Herein, an anionic adsorbent (HS-PAANa) was synthesized by grafting polyacrylic acid (PAA) onto the agricultural waste-hemp stem (HS). The obtained HS-PAANa adsorbent exhibited rapid adsorption kinetics, high adsorption capacity, and a favorable preference for cationic dyes, such as methylene blue (MB) and crystal violet (CV). The experimental data fit well with the pseudo-second-order kinetic model and Langmuir isotherm, demonstrating the efficiency of HS-PAANa in dye removal. Notably, the optimal adsorption capacities of HS-PAANa for MB and CV were found to be 1296.65 mg/g and 1451.43 mg/g, respectively. In the cationic/anionic dyes (MB/MO) binary systems, HS-PAANa exhibited enhanced selective adsorption of cationic dyes (MB), indicating its potential for targeted removal of specific dyes from mixed solutions. Moreover, HS-PAANa adsorption shows an excellent recyclability, after five cycles, HS-PAANa still maintained MB and CV removal rates of 93.85% and 95.08%, respectively. Therefore, the bioadsorbent HS-PAANa exhibits high potential as a highly efficient adsorbent for the effective treatment of cationic pollutants in wastewater., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this study, bamboo waste (BW) was subjected to pyrolysis-assisted ZnCl 2 activation to produce mesoporous activated carbon (BW-AC), which was then evaluated for its ability to remove cationic dyes, specifically methylene blue (MB) and crystal violet (CV), from aqueous environments. The properties of BW-AC were characterized using various techniques, including potentiometric-based point of zero charge (pH pzc ), scanning electron microscopy with energy dispersive X-rays (SEM-EDX), X-ray diffraction (XRD), gas adsorption with Brunauer-Emmett-Teller (BET) analysis, infrared (IR) spectroscopy. To optimize the adsorption characteristics (BW-AC dosage, pH, and contact time) of PBW, a Box-Behnken design (BBD) was employed. The BW-AC dose of 0.05 g, solution pH of 10, and time of 8 min are identified as optimal operational conditions for achieving maximum CV (89.8%) and MB (96.3%) adsorption according to the BBD model. The dye removal kinetics for CV and MB are described by the pseudo-second-order model. The dye adsorption isotherms revealed that adsorption of CV and MB onto BW-AC follow the Freundlich model. The maximum dye adsorption capacities ( q max ) of BW-AC for CV (530 mg/g) and MB (520 mg/g) are favorable, along with the thermodynamics of the adsorption process, which is characterized as endothermic and spontaneous. The adsorption mechanism of CV and MB dyes by BW-AC was attributed to multiple contributions: hydrogen bonding, electrostatic forces, π-π attraction, and pore filling. The findings of this study highlight the potential of BW-AC as an effective adsorbent in wastewater treatment applications, contributing to the overall goal of mitigating the environmental impact of cationic dyes and ensuring the quality of water resources.

Recently, several researchers have been trying to reduce the ecological effects of water pollution by considering the use of biodegradable materials that prevent the generation of secondary pollution in our environment and enable water reuse. Here, new biodegradable hydrogels based on alginate (Alg), gelatin (Gel) and polypyrrole (PPy) were successfully implemented to remove two known highly toxic cationic dyes from wastewater. The design process was performed in two steps: in-situ polymerization of polypyrrole within the Alg/Gel mixture, followed by hydrogel formation. Biocomposites showed promising efficacy for the removal of both basic red 46 (BR46) and crystal violet (CV) dyes from real and demineralized water samples. However, Alg-Gel-PPy hydrogel showed better selectivity for BR46 than for CV as compared to the pristine Alg-Gel hydrogel. Adsorption of both pollutants on biocomposite hydrogel beads followed the Langmuir isotherm and pseudo-second order kinetic models. Besides, the highest adsorption capacities (125 mg g -1 for BR46 and 88.5 mg g -1 for CV) were obtained for the Alg-Gel-PPy hydrogel, compared with those determined for PPy-free hydrogel (103.09 mg g -1 for BR46 and 86.96 mg g -1 for CV) and remained at a satisfactory level for five adsorption-desorption cycles. Finally, the obtained hydrogels showed excellent biodegradability by natural soil microorganisms, with 91 % decomposition., Competing Interests: Declaration of competing interest The authors report no declarations of interest., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Access to clean water is the mandatory requirement for every living being to sustain life. So, membrane-based integrated approach of adsorption and separation technology has recently been preferred by scientists over other conventional techniques, for wastewater treatment. Current research focused on the synthesis of novel imidazolium (A1) based IL, which was further functionalized with hydroxyapatite (HAp; extracted from Labeo rohita scales), to create possible solutions towards environmental remediation. Cellulose acetate (CA) was used for the fabrication of three different ionic liquid membranes. All the synthesized products were characterized by FTIR, XRD and TGA. Two dyes of different nature, i.e., congo red (anionic) and crystal violet (cationic) were selected because of their highly toxic and carcinogenic effects, for batch adsorption experiments. Antibacterial activity of the synthesized membranes was also evaluated against S. aureus. Results of the study revealed that CA-HA1 1:2 acted as the best adsorbent towards the removal of crystal violet, exhibiting removal efficiency of 98% with the contact time of 24 h while in case of congo red adsorption, CA-HA1 (1:2) proved as prime adsorbent with the removal efficiency of 96% for the same preceding contact time. Considering the antibacterial character of the synthesized membranes, CA-A1 (1:1) emerged as very efficient antibacterial agent with the inhibition zone of 50 mm after 48 h. The overall behavior of monolayer and multilayer adsorption was witnessed for both dyes while kinetic studies favored the pseudo-second order reaction for all adsorbents., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The present study is devoted to the removal of crystal violet dye using the synthesized barium alginate/carbon composites abbreviated as BA (barium alginate), BAAC (barium alginate/activated carbon), BASC (barium alginate/starch carbon), and BASSC (barium alginate/starch carbon modified with CTAB). The adsorptive removal of crystal violet as a function of contact time, pH of solution, composite dose, initial dye concentration, and temperature was studied. The uptake of crystal violet (CV) dye for the composites was recorded in the range of 36 mg g -1 to 50 mg g -1 at pH 8.03 ± 0.03 for an equilibrium time of 120 min. The adsorption kinetics and isotherms in compliance with the CV sorption onto BA/carbon composites corroborated the utmost fit of pseudo-second-order and Freundlich isotherm models, respectively. The recycling process was achieved using the barium alginate-treated bead carbons for different initial CV dye concentrations of 10-30 mg L -1 with a scope of zero disposal. The practicability of BA/carbon composites in a groundwater sample spiked with 30 mg L -1 of CV was successfully achieved with a removal efficiency of about 65-74%. Characterization studies for the composites using FTIR, SEM (with EDS), XRD, TGA, and BET were carried out and discussed in the paper., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this study, firstly, the syntheses and characterizations of biobased polyesters with different acid values obtained from the condensation reaction of biobased itaconic acid and polyethylene glycol were investigated. Then, UV curing was applied to form polymeric networks as adsorbent material from these polyesters containing different acids. Fourier transform infrared spectrometry (FTIR), Nuclear Magnetic Resonance Spectroscopy (NMR), X-ray Photoelectron Spectroscopy (XPS), Gel Permeation Chromatography (GPC) and scanning electron microscope (SEM) were used for the characterization of polymeric networks. The effects of the parameters of contact time, initial dye concentration, pH, temperature, amount of adsorbent on adsorption were investigated by batch method. In addition, adsorption equilibrium data were analyzed by Langmuir, Freundlich, Tempkin, Elovich, Redlich-Peterson, Harkin-Jura and Jossens adsorption models. Kinetic and thermodynamic studies were performed at 298, 308, 318 and 328 K and desorption studies were also examined. Comparison studies for the effects of the acid values of the adsorbent materials on the removal of methyl violet (MV) organic pollutant from aqueous solutions were analyzed. According to the pseudo-second-order model, the adsorption capacities were found to be ≥ 357.14 mg/g for the adsorbents. From the thermodynamic data, it was determined that the mechanism was exothermic and spontaneous. As a result of the third reuse, it was found that the adsorbents had a removal efficiency of ≥ 72.36%. According to the results observed the increase in the acidities in the chemical structure of bio-based polymeric networks enhances the adsoption properties., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The current study reports a facile method to fabricate functionalized multi-walled carbon nanotubes and montmorillonite clay mineral-based nanocomposite matrix and its detailed characterization using spectroscopic and morphological techniques. The nanocomposites have been studied for their potential applications in the treatment of contaminated water using batch adsorption studies. The investigations conducted using optical absorption spectroscopic measurements for the adsorption process indicate that the nanocomposite matrix can effectively remove almost 98% of the dye from aqueous solution. The nanocomposites have showed fast and strong adsorption behaviour for the dye with the maximum adsorption capacity (q m ) of ~467.3 mg g -1 in 25 min. The experimental data at equilibrium were also correlated with the theoretical adsorption isotherm and kinetic models. The results demonstrate that the experimental data fits well to the Freundlich adsorption isotherm model and conforms to second-order kinetics. Furthermore, the nanocomposite exhibits good recyclability without any marked decrease in the adsorption performance even after five adsorption cycles of usage which indicates its potential application as reusable adsorbent for the efficient removal of hazardous dyes from contaminated water., (© 2022 John Wiley & Sons Ltd.)

In this study, an environmentally sustainable process of crystal violet, congo red, methylene blue, brilliant green, Pb 2+ , Cd 2+ , and Zn 2+ ions adsorption from aqueous solutions onto amino-modified starch derivatives was investigated. The degree of substitution, elemental analysis, swelling capacity, solubility, and FTIR, XRD, and SEM techniques were used to characterize the adsorbents. The influence of pH, contact time, temperature, and initial concentration has been studied to optimize the adsorption conditions. The amino-modified starch was the most effective in removing crystal violet (CV) (65.31-80.46 %) and Pb 2+ (67.44-80.33 %) within the optimal adsorption conditions (pH 5, 10 mg dm -3 , 25 °C, 180 min). The adsorption of CV could be described by both Langmuir and Freundlich adsorption isotherms, while the adsorption of Pb 2+ ions was better described by the Langmuir isotherm. The pseudo-second order model can be used to describe the adsorption kinetics of CV and Pb 2+ on all tested samples. The thermodynamic study indicated that the adsorption of CV was exothermic, while the Pb 2+ adsorption was endothermic. The simultaneous removal of CV and Pb 2+ from the binary mixture has shown their competitive behavior. Thus, the amino-modified starch is a promising eco-friendly adsorbent for the removal of dyes and heavy metals from polluted water., Competing Interests: Declaration of competing interest There are NO known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Water is the most important resource for life, but it has been greatly exhausted over the past century as a result of the human population and environmentally harmful activities. The excessive quantity of dyes exists in the wastewater produced from the textile industries which is the main reason for serious human health and environmental problems. There are many dye removal techniques, and the most promising one is the adsorption technique. The novelty of this research is using unmodified synthesized hydroxyapatite (HAp) as an adsorbent for the removal of gentian violet (GV) dye from aqueous solutions as there are no sufficient data in the literature about using it in the adsorption of GV dye from aqueous solutions. Unmodified HAp was synthesized by a combined precipitation microwave method. The prepared adsorbent was characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and zeta potential analyses. The kinetic study showed that the pseudo-second-order (PSO) model was the best fitted model with the experimental data. Analysis of adsorption isotherms using different models showed that this adsorption system was better described by the Halsey isotherm with a maximum adsorption capacity ( q max )  of 1.035 mg/g. The effects of experimental factors such as initial solution pH, initial dye concentration, adsorbent dose, and contact time were studied during the investigation of GV dye removal efficiency. The experimental results indicated that the maximum adsorption efficiency (99.32%) of the GV dye using HAp adsorbent was achieved at the following conditions: contact time = 90 min, pH = 12, initial GV dye concentration = 3 mg/L, and adsorbent dose = 1 g/L. The adsorption mechanism of the GV dye using HAp might be explained by the electrostatic interaction between the negatively charged surface of the HAp and the positively charged group of the GV dye. Thermodynamics study was performed on the adsorption process of GV dye from aqueous solutions using the synthesized HAp which revealed that this process was endothermic and spontaneous due to positive values of Δ H and Δ S and negative values of Δ G ., Competing Interests: The authors declare that they have no conflicts of interest., (Copyright © 2023 Dalia A. Ali et al.)

In this study, activated carbon produced from oak cupules (ACOC) was prepared using chemical activation with H 3 PO 4 . ACOC is subsequently used as an adsorbent to facilitate the removal of an acidic dye, naphthol blue black (NBB), and basic dye crystal violet (CV) from aqueous solutions. The ACOC was characterized by FTIR spectroscopy, XRD, and SEM. The adsorption isotherm data fits well with the Langmuir model for NBB and CV. The kinetic models of adsorption of NBB and CV by ACOC were pseudo-first order and pseudo-second order, respectively. Thermodynamic parameters were evaluated and indicated that the adsorption of both dyes onto ACOC was endothermic and spontaneous. The adsorption capacity of ACOC reached 208 mg g -1 for NBB and 658 mg g -1 for CV. ACOC was shown to be a promising adsorbent for the removal of NBB and CV from aqueous solutions.

In the present study, biomass from the Chromolaena odorata plant's stem was activated using sulfuric acid to adsorb crystal violet (CV) dye. The adsorption operation of CV dye was studied considering the effect of variables like pH, initial dye concentration, time, adsorbent dosage, and temperature. The pseudo-second-order equation best fitted the kinetic study. The thermodynamic parameters such as activation energy (9.56 kJ/mol), change in Gibbs energy (81.43 to 96.7 kJ/mol), enthalpy change (6.89 kJ/mol), and entropy change (-254.4 J/mol K) were calculated. Response surface methodology estimated that at pH (4.902), adsorbent dosage (8.33 g/L), dye concentration (82.30 ppm), and temperature (300.13 K) dye removal of 97.53% is possible. FTIR, SEM, XRD, BJH, and BET confirmed adsorption operation. The adsorbent can be reused for 3 cycles effectively. Langmuir isotherm which best fitted the adsorption operation was used for designing a theoretical single-stage batch adsorber for large-scale operation., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this study, cottonwood seeds (CWS) were introduced as a novel, green, and low-cost biosorbents for the removal of crystal violet (CV) dye from aqueous solutions. To illustrate the characteristics of CWS, surface morphology, Fourier-transform infrared spectroscopy, field emission scanning electron microscopes, and energy dispersive X-ray spectroscopy techniques were employed. Important adsorption variables ( i.e. , equilibrium time, solution pH, CWS amount, CV concentration, and temperature) were systematically studied. Maximum CV dye adsorption was observed at pH 10 using 20 mg of the adsorbent. Different adsorption isotherms were investigated, and the results were more accurately consistent with the Langmuir model ( R 2 = 0.992). The maximum capacity of adsorption was 153.85 mg g -1 at 60 min. The kinetic data were examined by different models and a pseudo-second-order model supplied the best correlation between experimental data. Investigated thermodynamic parameters at different temperatures illustrated that the CV adsorption procedure was spontaneous and endothermic with an increase in entropy. The percentage removal and the relative standard deviations for the real sample analysis were in the range of 89-98% and 4.9-9.5%, respectively. High adsorption capacity and low equilibrium time demonstrated that CWS is an impressive biosorbent for dye pollutants uptakes from aqueous solutions and real industrial wastewater samples.

Fallen bamboo leaves ( Bambusa bambos ), hereinafter BL have been designed to be transformed into an efficient and sustainable adsorbent for the removal of crystal violet (CV) dye from wastewater with up to 95% scavenging ability. BL have been characterized by Fourier transform infrared (FTIR) spectra, field emission scanning electron microscopy (FESEM), and zero point charge (pHzpc). The maximum adsorption capacity is 30 mg/g at pH 10. Physico-chemical parameters have been investigated concerning pH, contact time, initial concentration, and coexistent ions. Pseudo-second-order kinetics is followed best ( R 2 =0.999) signifying a chemisorption pathway. Besides, intra-particle diffusion plays a governing role in the film diffusion of crystal violet into the core of the adsorbent. Langmuir isotherm model fits best ( R 2 =0.972) suggesting a uniform, monolayer, and homogeneous adsorption. Regeneration was successful with methanol (65%) and reusability was tested for three cycles and was found to retain activity up to 80%. Analysis of CV containing industrial effluent suggests that a 36.8% reduction is possible with BL. The effect of co-existent ions suggests little influence on the adsorption. Compared to other contemporary and relevant adsorbents, it can be concluded that BL can be exercised for the sustainable decontamination of CV-containing wastewater.

In this study, the biomass of rubber seed pericarp was first treated with sulfuric acid and then its activated carbon was formed by the pyrolysis process. As produced acid-treated activated carbon of chosen biomass was then used for the adsorption of crystal violet (CV) and methylene green (MG) from the colored aqueous solution. The adsorbent was exposed to several characterization methods to know its structural and morphological behaviors before and after CV and MG adsorption. The adsorbent was found to be mesoporous having a surface area of 59.517 m 2 /g. The effect of pH, time, and concentration was assessed while various isotherm and kinetics models were employed to know the adsorption insight. The optimum conditions were at pH 8, within 30 min, 50 mg/L concentration, and 0.06 gm dose. The adsorption data (the maximum adsorption capacity for CV and MG were found to be 302.7 and 567.6 mg/g, respectively) was validated by fitting in a response surface statistical methodology and the positive interactions between the studied factors were found. The adsorption was mainly belonging to the electrostatic attraction of the dye molecules. The study proves that the used adsorbent is economical and an excellent source of treating wastewater.

In this study, the performance of the montmorillonite-filled sodium alginate/gelatin (SA-GEL-MMT) ternary biocomposite microbeads on the adsorptive removal of crystal violet (CV) dye was investigated. Firstly, the composites containing different weight ratios of MMT such as 10 %, 15 %, and 20 % were prepared. The composite beads were cross-linked using a calcium chloride (3%wt/v) solution. To determine the optimum sorption conditions the studies were performed at different parameters namely temperature, pH, contact time, sorbent dose, and dye concentration. From the sorption studies, the maximum capacity of the microbeads was found as 1000.0 mg/g whereas the maximum removal of the dye was 92.1 % at pH = 7 and a temperature of 25 °C. Additionally, the kinetic studies showed that the sorption of the dye followed the pseudo-second-order kinetics. Moreover, the adsorptive removal of the dye occurs spontaneously. This study suggests that the use of SA-GEL-MMT can be highly effective and reusable for the treatment of wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Current work focuses on fabricating a new bio-nano adsorbent of Fe 3 O 4 @inulin nanocomposite via an in-situ co-precipitation procedure to adsorb methyl orange (MO) and crystal violet (CV) dyes from aqueous solutions. Different physical characterization analyses verified the successful fabrication of the magnetic nanocomposite. The adsorbent performance in dye removal was evaluated by varying initial dye concentration, adsorbent dosage, pH and temperature in 5110 mg/L, 0.10.8 g/L, 111 and 283-338 K, respectively. Due to the pH of zero point of charge and intrinsic properties of dyes, the optimum pHs were 5 and 7 for MO and CV adsorption, respectively. The correlation of coefficient (R 2 ) and reduced chi-squared value were the criteria in order to select the best isotherm and kinetics models. The Langmuir model illustrated a better fit for the adsorption data for both dyes, demonstrating the maximum adsorption capacity of 276.26 and 223.57 mg/g at 338 K for MO and CV, respectively. As well, the pseudo-second-order model showed a better fitness for kinetics data compared to the pseudo-first-order and Elovich models. The thermodynamic parameters exhibited that the dye adsorption process is endothermic and spontaneous, which supported the enhanced adsorption rate by increasing temperature. Moreover, the nanocomposite presented outstanding capacity and stability after 6 successive cycles by retaining more than 87% of its initial dye removal efficiency. Overall, the magnetized inulin with Fe 3 O 4 could be a competent adsorbent for eliminating anionic and cationic dyes from water., (© 2022. The Author(s).)

In this study, ex-situ crosslinked gellan gum (GG)/bacterial cellulose (BC) hydrogels have been investigated as good absorbents for the removal of safranin and crystal violet dye pollutants. The preparation involves a cost-effective and easy-to-perform crosslinking procedure, using citric acid (CA) as a green crosslinker. The physicochemical and mechanical properties of the crosslinked hydrogels were examined by FTIR, TGA, SEM, XRD, and unconfined compression analyses. The swelling capacity of the hydrogels as a function of pH was investigated. CA depicted to improve structural stability as a crosslinker. The dye removal capacity of the hydrogels as good adsorbents was explored and showed higher efficiency in the removal of safranin dye as compared to crystal violet with optimum adsorption capacities obtained as 17.57 and 13.49 mg/g, respectively. Adsorption kinetics and isotherm models as well as thermodynamics examined. Results showed the adsorption process well fitted the pseudo 2nd-order kinetic and Langmuir-Freundlich models while temperature dependence study depicted to be exothermic. Furthermore, no significant loss of removal efficiency of the hydrogel adsorbent was observed even after five adsorption-desorption cycles. Based on the revealed results, the prepared hydrogel may serve as an effective adsorbent for the removal of dyes from the aqueous phase., Competing Interests: Declaration of competing interest The authors declare no conflict of interest in the present study., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Natural clay (NC) was employed as a natural adsorbent for the elimination of an azo dye Crystal Violet (CV) from aqueous media. The characterization of the clay was performed by X-ray diffractometry (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM) equipped with an X-ray energy dispersion spectrometer (EDS) and Brunauer-Emmett-Teller (BET) specific surface area analysis. The Box-Behnken design (BBD) was used as a powerful tool to determine the stationary points of the main independent factors: initial CV concentration, initial pH, temperature, and adsorbent dose on the adsorption efficiency. The significance and adequacy of the model were investigated using analysis of variance (ANOVA). The obtained results indicated an optimal dye removal of 99.1% at pH = 3, initial CV concentration of 11.767 mg/L, adsorbent load of 3.075 g/L, and T = 298.0 K. The kinetic study was evaluated using three models: a pseudo-first-order (PFO), a pseudo-second-order (PSO), and an intraparticle diffusion model. The observed kinetics is in excellent agreement with the PSO kinetic model. Therefore, both isotherms Langmuir and Freundlich fitted well the adsorption equilibrium data. The thermodynamic study revealed that the main parameters including (ΔG°, ΔH°, and ΔS°) indicated that the adsorption of CV onto NC was an endothermic and spontaneous process., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The motive of this work is to synthesis aromatic polyimides by a two-step poly condensation process and the prepared aromatic polyamides (APIs) is been used as an effective functionalized adsorbent for the removal of carcinogenic crystal violet (CV) from aqueous medium. The adsorption efficiency of the APIs was enhanced by incorporation different functional moieties (varying aromatic dianhydrides with -O-, -(CF 3 ) 2 -, -(CH 3 ) 2 -) in the polymer structure. The initial and final concentration of CV was measured using UV-Vis spectrometer. The adsorption process was optimized by varying the parameters such as the effect of solution pH, contact time, initial dye concentration, and adsorbent dosage. Kinetics and isotherms of the adsorption system were appraised using data obtained from effect of contact time and initial dye concentration with corresponding empirical modelling techniques respectively. The evaluated results of the adsorption kinetic studies confirmed that the adsorption of API onto CV is followed a pseudo-second-order kinetic model. The adsorption behaviour and their interactions between APIs and CV are well established. The experimental results of this research output could be confirmed that APIs is a very effective adsorbent for the removal of cationic dye from aqueous., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

In the present study, alginate@silver nanoparticles (Alg@AgNPs) bionanocomposite has been fabricated successfully and further explored for the removal of crystal violet (CV) dye from the aqueous solution. The surface morphology of the (Alg@AgNPs) bionanocomposite was characterized by various modern analytical techniques such as SEM-EDX, TEM, FTIR and XRD. The maximum adsorption was observed at optimum condition of (pH 7, adsorbent dose 0.01 g, equilibrium time 240 min and initial concentration 20 mg L -1 ). The maximum monolayer adsorption capacity was found to be 186.93 mg g -1 at 30 °C. The experimental data were further validated by various isotherm models and on the basis of highest correlation coefficient (R 2 , 0.99), Langmuir model was found to be best fitted model. Pseudo-second order kinetic model obeyed best for the experimental data with a highest correlation coefficient (R 2 , 0.99) at all studied temperature. In thermodynamic studies, the positive value of enthalpy change (∆H 0 ) and entropy change (∆S 0 ) confirmed the process to be endothermic and spontaneous in nature. Desorption studies shows that 83 % of the adsorbed CV can be desorbed in first cycle and can be regenerated up to 4th cycle effectively with 0.1 M HCl. Therefore, (Alg@AgNPs) bionanocomposite could be harnessed as a potential adsorbent for the removal of hazardous CV dye from the waste water., (Copyright © 2022. Published by Elsevier B.V.)

A novel fabrication of magnetite (Fe 3 O 4 ) nanochains, surface functionalized with glutathione (GSH), has been attempted through a basic wet reduction method, coalesced with oxidative etching for the removal of crystal violet (CV) and phenol red (PR) from an aqueous solution. The structural and functional characterizations of GSH@Fe 3 O 4 MNPs were performed using SEM-EDX, DLS, XRD, and FTIR. The nanochain-structured adsorbent was found to have an average size of 24 ± 1.29 nm and a zeta potential value of - 6.44 mV. The batch experiments showed that GSH@Fe 3 O 4 MNPs have a brilliant removal efficiency of 97% and 79% for CV and PR dyes, respectively, within a period of 60 min. The influence of different operational parameters like adsorbent dosage, pH, temperature, reaction time, and initial dye concentration on the removal behaviour of the adsorbent was studied in detail. The adsorbate-adsorbent reaction was tested over isotherm models, and the reaction fitted well for Langmuir isotherm with an excellent q max value of 1619.5 mg/g and 1316.16 mg/g for CV and PR dye, respectively. The experimental results were also validated using different reaction kinetics, and it was found that the pseudo-first-order model fits well for PR dye adsorption (R 2 = 0.91), while adsorption of CV dye was in best agreement with the pseudo-second-order kinetic model (R 2 = 0.98). Thermodynamic studies revealed that the adsorption reaction was spontaneous and endothermic in nature. Furthermore, GSH@Fe 3 O 4 MNPs can be reused effectively up to 5 cycles of dye removal. Major mechanisms involved in the adsorption reaction were expected to be electrostatic attraction, hydrogen bonding, and π-interactions. The efficiency of GSH@Fe 3 O 4 MNPs in real water samples suggested that it has a high potential for dye removal from complex aqueous systems and could be used as an effective alternative for remediation of dyes contaminated water., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The discharge of large amounts of effluents contaminated with gentian violet (GV) and phenol red (PR) threatens aquatic flora and fauna as well as human health, which is why these effluents must be treated before being discarded. This study seeks the removal of dyes, using water lily ( Eichhornia crassipes ) as an adsorbent with different pretreatments. PR and GV were analyzed by a UV-visible spectrophotometer. Equilibrium experimental data showed that Freundlich is the best model to fit PR and SIPS for GV, showing that the adsorption process for both dyes was heterogeneous, favorable, chemical (for GV), and physical (for PR). The thermodynamic analysis for the adsorption process of both dyes depends directly on the increase in temperature and is carried out spontaneously. The Pseudo first Order (PFO) kinetic model for GV and PR is the best fit for the dyes having an adsorption capacity of 91 and 198 mg/g, respectively. The characterization of the materials demonstrated significant changes in the bands of lignin, cellulose, and hemicellulose, which indicates that the functional groups could participate in the capture of the dyes together with the electrostatic forces of the medium, from which it be concluded that the adsorption process is carried out by several mechanisms.

The focus of this work was on developing a green, low-cost, and efficient biosorbent based on the biological structure and properties of MT and applying it to the remediation of cationic dyes in dye wastewater. The adsorption performance and mechanism of MT on methylene blue (MB) and crystal violet (CV) were investigated by batch adsorption experiments. The results demonstrated that the highest adsorption values of MT for MB (411 mg/g) and CV (553 mg/g) were greatly higher than the reported values of other biosorbents. In addition, the adsorption behaviors of methylene blue (MB) and crystal violet (CV) by MT were spontaneous exothermic reactions and closely followed the pseudo-second-order (PSO) kinetics and Langmuir isotherm. Further, the depleted MT was regenerated using pyrolysis mode to convert depleted MT into MT-biochar (MBC). The maximum adsorption of Cu 2+ and Pb 2+ by MBC was up to 320 mg/g and 840 mg/g, respectively. In conclusion, this work presented a new option for the adsorption of cationic dyes in wastewater and a new perspective for the treatment of depleted biosorbents.

In this study, hydrochar-based-eggshell was prepared via the subcritical water medium (SCWM) and used as a catalyst in the thermally activated peroxide oxidation (TAPO) approach for crystal violet and dye bathing wastewater degradation. The catalytic activities for the raw eggshell (RES) and hydrochar-based-eggshell (HES) were compared. RES and HES were characterized using a scanning electron microscope (SEM),energy-dispersive X-ray spectroscopy (SEM-EDX), and Fourier transforms infrared spectroscopy (FT-IR). The affecting parameters on the degradation process were optimized using response surface methodology (RSM). The effects of temperature (293-333 K), amount of catalyst (5-25 mg/50 mL), the concentration of H 2 O 2 (0-8 mM), and treatment time (10-70 min) on the TAPO method were investigated using central composite design (CCD). For the crystal violet removal, two models were developed. Both models were significant and can be used to describe the design space. Also, the dye bathing wastewater degradation was described by another developed model, which had a high correlation coefficient (R 2  = 0.97). In general, catalytic activity for HES was higher than RES. The degradation of crystal violet reached 98.10% when a 20 mg HES catalyst and 6 mM H 2 O 2 at 323 K for 55 min were used. While 97% of the color of dye bathing wastewater was removed in 55 min at 323 K using 25 mg of HES and 4 mM H 2 O 2 . This study showed that the hydrolyzed eggshells could be used in the oxidation of crystal violet and dye bathing wastewater by the thermally activated peroxide oxidation method., (Copyright © 2022 Elsevier Inc. All rights reserved.)

In this study, a polysaccharide-based hydrogel microsphere (SFP/SA) was prepared using S. fusiforme polysaccharide (SFP) and sodium alginate (SA). Fourier transform infrared spectroscopy (FT-IR) demonstrated that SFP was effectively loaded onto the hydrogel microsphere. Texture profile analysis (TPA) and differential scanning calorimetry (DSC) showed that, with the increase of SFP concentration, the hardness of SFP/SA decreased, while the springiness and cohesiveness of SFP/SA increased, and the thermal stability of SFP/SA improved. The equilibrium adsorption capacity of SFP/SA increased from 8.20 mg/g (without SFP) to 67.95 mg/g (SFP accounted 80%) without swelling, and from 35.05 mg/g (without SFP) to 81.98 mg/g (SFP accounted 80%) after 24 h swelling. The adsorption of crystal violet (CV) dye by SFP/SA followed pseudo-first order and pseudo-second order kinetics (both with R2 > 0.99). The diffusion of intraparticle in CV dye was not the only influencing factor. Moreover, the adsorption of CV dye for SFP/SA (SFP accounted 60%) fit the Langmuir and Temkin isotherm models. SFP/SA exhibited good regenerative adsorption capacity. Its adsorption rate remained at > 97% at the 10th consecutive cycle while SFP accounted for 80%. The results showed that the addition of Sargassum fusiforme polysaccharide could increase the springiness, cohesiveness and thermal stability of the hydrogel microsphere, as well as improve the adsorption capacity of crystal violet dye.

A novel modified rice husk (MRH) has been prepared for removing cationic dyes in both single system and binary system. SEM-EDS, FT-IR, XRD and XPS were used to characterize the physical and chemical properties of MRH. It showed that the maximum adsorption capacity of MRH for methyl violet (MV) and malachite green (MG) in single system was 154.49 and 996.97 mg g -1 , while in binary system was 530.94 and 408.58 mg g -1 , respectively. The experimental results showed that the pseudo-second-order kinetic model was better to describe the kinetic behavior of MV and MG adsorption. By using double layer adsorption model, we found that the n D for MV adsorption were 2.52, 2.65 and 3.34 at 298, 308 and 318 K, respectively, and the n D for MG adsorption were 4.59, 4.85 and 4.30, respectively. These results illustrated that multiple dye molecules were adsorbed on one adsorption site in non-parallel direction, indicating that the adsorption of dyes is multi-molecular mechanism. Furthermore, synergistic and antagonistic adsorption might be existed simultaneously in binary system. In summary, MRH has been shown well adsorption properties and reusability and our finding might provide a new idea for developing low-cost, efficient and reusable adsorbent to remove dyes from wastewater., (Copyright © 2022 Elsevier B.V. All rights reserved.)

In this work, attapulgite (ATP)-based dual sensitive poly (N-isopropylacrylamide-co-acrylic acid) composite hydrogel, P(NIPAM-co-AA)/ATP, was prepared by free radical polymerization. The prepared composite hydrogel was characterized via methods of scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), zeta potential analysis and Brunauer, Emmett, and Teller (BET) etc. The composite hydrogel showed pH and temperature sensitive behaviour, with lower critical solution temperature (LCST) of 35°C and highest swelling occurred at pH 8.0. The adsorption of methyl violet (MV) can be controlled by the hydrogel responsiveness, and 95.78% of MV can be removed at pH 8.0 and 35°C. The addition of a small amount of ATP (3 Wt%) can improve the swelling ratio and adsorption capacity. Kinetic analysis demonstrated that the experimental data were best fitted to the pseudo-second order model. Isotherm analysis showed that the equilibrium data followed Langmuir model with the adsorption capacity of 168.35 mg g -1 . In addition, the composite hydrogel has high adsorption selectivity for cationic dyes, and MV-loaded hydrogel is easy to regenerate, which can be used for successive adsorption cycles. These results demonstrate that the composite hydrogel has potential application in dye wastewater treatment.

Metal-organic frameworks (MOFs) have received extensive attention in adsorption applications owing to their high surface area. However, some MOFs do not perform well as the extraction medium when used under aqueous conditions. The low hydrostability of MOFs limits the practical application of these materials in solid-phase microextraction (SPME). Here, the fabrication of a water resistance SPME fiber coating is introduced based on the crystal violet (CV)-modified HKUST-1 framework on copper (Cu@HKUST-1@CV). The HKUST-1 was prepared by the in situ growth method, followed by post-synthetic modification of HKUST-1 with the CV layer. The preparation of the modified HKUST-1 was characterized by FESEM, XRD, FTIR, and DFT approaches. The prepared SPME coating was successfully employed for the quantification of anthracene (AN), as a model analyte, in water samples. The limit of detection was 0.8 ng mL -1 . The developed method will open up a new door towards searching for promising materials in SPME applications., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

In this research, an efficient sorbent based on poly(β-cyclodextrin-ester)-functionalized silica-coated magnetic nanoparticles (MNPs-CDP) was prepared and used for magnetic solid-phase extraction of the malachite green (MG) and crystal violet (CV) from water samples prior to their determination by high-performance liquid chromatography-ultra violet detection (HPLC-UV). The synthesized nanoparticles were characterized by the field emission-scanning electron microscopy (FE-SEM) and Fourier transform infrared spectroscopy (FT-IR). Of course, the factors, which could influence the extraction efficiency like pH, sorbent amount, salt content, extraction time, desorption time, eluent type, and volume and sample volume, were optimized by response surface methodology. Then, for both of MG and CV, good linearity (0.1-200 μg L -1 , r 2  ≥ 0.99) was achieved under the optimized conditions. The limits of detection (LODs) and the limits of quantification (LOQs), for both of MG and CV, were 0.03 μg L -1 and 0.1 μg L -1 , respectively. Precision of the method expressed as the relative standard deviations (RSDs) at concentration level of 100 μg L -1 was 5.6 and 4.2 for MG and CV, respectively. Ultimately, usability of proposed method was investigated by analysis of CV and MG in tap water, fish pond water, and the lake water, and the satisfactory recoveries were obtained in the range of 92-100.5%.

The main aim of this study was to ascertain the photocatalytic degradation of organic pollutants present in aqueous phase using fluorescent biogenic ZnS nanocolloids produced from an endophytic fungus Aspergillus flavus. The degradation studies were carried out using different organic pollutants such as methyl violet (MV), 2,4-dichlorophenoxyacetic acid (2,4-D) and paracetamol (PARA) for 120 min, 270 min and 240 min, respectively, at pH varying from 3.0 to 11.0. The results from this study indicate that the degradation efficiency of ZnS nanocolloids for MV, 2,4-D and PARA were 87%, 33% and 51%, respectively, at the optimum concentration of 100 mg/L of the tested organic pollutants. At different time intervals, the samples were analyzed for their chemical oxygen demand (COD) and total organic carbon (TOC) contents. The reduction of COD and TOC were 78% and 74% for MV at 120 min; 55.5% and 57.2% for 2,4-D at 270 min and 47.6% and 44.5% for PARA at 240 min, respectively. The degradation pathway was determined based on the mass spectrum and the intermediates formed; in addition, the interaction between organic pollutants and nanocolloids was also elucidated based on atomic force microscopy (AFM) and fluorescence spectrum., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In this study, a novel biocomposite beads is developed by gelling sodium alginate (ALG) solutions in acid whey (Aw). The formation of alginate-whey biocomposite (ALG-Aw) was confirmed by FTIR analysis where the corresponding spectrum showed the presence of characteristic absorption bands of both ALG and Aw. SEM analysis showed the presence of lactic bacteria immobilized in the alginate matrix leading to the formation of new porous structure. The adsorption properties of adsorbents were evaluated in crystal violet dye (CV) removal from aqueous solutions using a batch adsorption technique. The results showed that the maximum adsorption occurred at pH 6 and for an adsorbent dose of 0.4 g/L. The kinetic of CV removal onto ALG-Aw adsorbent can be described well by the pseudo-second order equation. The equilibrium adsorption data of ALG-Aw followed well the Redlich-Peterson isotherm which is coherent with the calculated R 2 , χ 2 and ARE values. Calculated thermodynamic parameters such as Gibbs free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) shown that adsorption reaction is spontaneous and it is favored at low temperatures. Interactions of CV dye molecules with ALG-Aw composite beads were examined by FTIR and UV-visible DR spectroscopy., (Copyright © 2019 Elsevier B.V. All rights reserved.)