Amputation of Remazol brilliant blue dye on crosslinked chitosan hydrogel: Statistical treatment and experimental evaluation.

The primary aim of this research is to comprehensively assess the applicability of chitosan biopolymer towards water treatment application and to enhance its adsorption capacity towards Remazol brilliant blue R-19 dye. This has been achieved through physical modification to obtain the material in hydrogel form and chemical modification by crosslinking it with barbituric acid. The characterization of the resulting Chitosan-barbituric acid hydrogel (CBH) was carried out using various analytical techniques such as SEM-EDX, FT-IR, TGA-DTA, XRD, and BET. CBH was employed as the adsorbent to eliminate R-19 dye from aqueous media. Utilizing response surface methodology (RSM), the parameters were fine-tuned, leading to the achievement of more than a 95% removal for R-19 dye. The adsorption behavior closely adhered to the Langmuir isotherm and pseudo-second-order kinetics. An interesting observation indicated that the rise in temperature leads to rise in adsorption capacity of CBH. The maximum adsorption capacities evaluated at 301.15 K, 313.15 K, 318.15 K, and 323.15 K were 566.6 mg g-1, 624.7 mg g-1, 671.3 mg g-1, and 713.5 mg g-1 respectively, in accordance with the Langmuir isotherm model. Examining the thermodynamics of the adsorption process revealed its spontaneous nature (ΔG = -21.14 to -27.09 kJ mol-1) across the entire temperature range. Furthermore, the assessment of the isosteric heat of adsorption (ΔHads) was conducted using the Clausius-Clapeyron equation, with results indicating an increase in ΔHads from 1.85 to 2.16 kJ mol-1 with temperature rise from 301.15 K to 323.15 K due to augmented surface loading. This suggested the existence of lateral interactions between the adsorbed dye molecules. The potential of adsorbent for regeneration was investigated, demonstrating the ability to reuse the material. Sustainability parameter calculated for synthesis process reflected a notably low E-factor value of 0.32 demonstrated the synthesis is environment friendly.

Process optimization of adsorptive phytoremediation of mutagenic brilliant green dye for health risk management using chemically activated Symplocos racemosa agro-waste.

Textile industries use large amounts of water as well as dyes. These dyes containing water are then discharged into the water bodies causing a significant role in water pollution. Brilliant Green dye contributes to many harmful diseases related to the respiratory and gastrointestinal tract. In this study, Symplocos racemosa (SR) agro-waste was chemically treated with acid (SR-HCl) and base (SR-NaOH) and then used for removing Brilliant Green Dye (BGD) on the batch scale. They were characterized by SEM, EDX, FTIR, XRD, TGA and DSC. Optimized conditions were 30 °C temperature, pH 6, adsorbent dose of 0.10 g/25 ml dye solution, shaking speed of 100 revolutions per minute, initial dye concentration of 50 ppm and 35 min time for shaking adsorbent and dye solution. Adsorption data obtained were analyzed using isotherms. The experimental data was found to fit well with the Langmuir model and the maximum adsorption capacity (qmax) of BGD on the SR, SR-HCl, and SR-NaOH was revealed to be 62.90, 65.40, and 71 mg/g respectively. Kinetic data (pseudo-first-order and pseudo-second-order) were evaluated and adsorption tends to follow the pseudo-2nd-order, which indicated the chemisorption mechanism. The results revealed that Symplocos racemosa agro-waste can be considered as the potential biosorbent.

Theoretical Study of Copper Squarate as a Promising Adsorbent for Small Gases Pollutants.

Copper squarate is a metal-organic framework with an oxo-carbonic anion organic linker and a doubly charged metal mode. Its structure features large channels that facilitate the adsorption of relatively small molecules. This study focuses on exploring the potential of adsorbing small pollutants, primarily greenhouse gases, with additional investigations conducted on larger pollutants. The objective is to comprehend the efficacy of this new material in single and multiple molecular adsorption processes using theoretical methods based on density functional theory. Furthermore, we find that the molecular adsorption energies range from 3.4 KJ∙mol-1 to 63.32 KJ∙mol-1 depending on the size and number of adsorbed molecules. An exception is noted with an unfavorable adsorption energy value of 47.94 KJ∙mol-1 for 4-nitrophenol. More importantly, we demonstrate that water exerts an inhibitory effect on the adsorption of these pollutants, distinguishing copper squarate as a rare MOF with hydrophilic properties. The Connolly surface was estimated to give a more accurate idea of the volume and surface accessibility of copper squarate. Finally, using Monte Carlo simulations, we present a study of adsorption isotherms for individual molecules and molecules mixed with water. Our results point out that copper squarate is an efficient adsorbent for small molecular pollutants and greenhouse gases.

Adsorption of azo dye by biomass and immobilized Yarrowia lipolytica; equilibrium, kinetic and thermodynamic studies.

One of the major environmental problems we have today is dye pollution, primarily caused by the textile industry. This pollution has detrimental effects on aquatic life, soil fertility, and human health. Many microbial biosorbents have been documented in the literature for the removal of a wide range of azo dyes commonly employed in the textile industry. However, Yarrowia lipolytica NBRC1658 is firstly used as both free and immobilized sorbents for the removal of Reactive yellow 18 (RY18), acid red 18 (AR18) and basic blue 41 (BB41) in this study. The effect of experimental conditions such as pH, biosorbent quantity, dye concentration, contact time, and temperature on dye removal capacity are examined. The research findings demonstrate that the adsorption capacity is higher in biomass compared to immobilized cells. The highest adsorption capacities are observed at pH 2 for RY18 and AR18, while pH 9 is optimal for BB41. Increasing the adsorbent dosage and initial concentration significantly improves the adsorption capacity. The Langmuir model best describes the adsorption process, indicating that the dye attaches to the biosorbent in a single layer, with a uniform biosorbent surface. The removal of the dye occurs through a chemical process on the biosorbent surface, as evidenced by the pseudo-second-order kinetic model. According to thermodynamic analysis, higher temperatures promote greater adsorption of dyes. Our study shows the effectiveness of Yarrowia lipolyica NBRC1658 as a biosorbent in the removal of a wide range of industrial dyes.

Removal of fluorouracil from aqueous environment using magnetite graphene oxide modified with γ-cyclodextrin.

Fluorouracil (FU) is a widely utilized antineoplastic medication in the pharmaceutical industry for combating gastrointestinal cancers. However, its presence in wastewater originating from pharmaceutical facilities and hospital effluents has a potential effect on DNA, and cannot be efficiently eliminated through conventional treatment methods. Consequently, the adoption of advanced technologies becomes crucial for effectively treating such wastewater. Accordingly, this study investigated the efficiency of magnetite graphene oxide nanocomposite functionalized with γ-cyclodextrin for removing fluorouracil from aqueous solutions. The magnetite graphene oxide nanocomposite functionalized with γ-cyclodextrin was synthesized via the hydrothermal method. Next, the effect of pH, temperature, adsorbent content, and contact time on the fluorouracil removal efficiency was explored. Ultimately, the experimental data were matched against Langmuir, Freundlich, and Temkin isotherms and Kinetic models. Accordingly, the efficiency of the absorbent used was dependent on the pH, contact time, temperature, and initial concentration of the adsorbent. The results indicated that the maximum removal efficiency for fluorouracil was achieved within the contact time of 45 min and adsorbent content of 0.020 g. In addition, the optimal pH for removing the medicine was 7. The conditions of the adsorption process followed Langmuir isotherm with correlation coefficients of 0.992 and a quasi-second kinetic model with a correlation coefficient of 0.999, with the maximum adsorption capacity of the adsorbent synthesized for the evaluated medicine estimated as 190.9 mg/g. The results showed that the magnetite graphene oxide nanocomposite functionalized with γ-cyclodextrin could be used as an effective and available adsorbent for removing fluorouracil from pharmaceutical wastewater.

Coupling of carboxymethyl starch with 2-carboxyethyl acrylate: A new sorbent for the wastewater remediation of methylene blue.

Textile and printing industries play a vital role in the economy of any country. But the effluents of these industries, which contain toxic Methylene Blue (MB) dye when mixed with fresh water, make it unfit for human health and aquatic life. For the removal of MB, different adsorbents were used, but they were expensive, non-biodegradable or less effective. In this research, novel carboxymethyl starch grafted poly 2-carboxyethyl acrylate (CM-St-g-P2CEtA) was synthesized by reacting carboxymethyl starch with 2-carboxyethyl acrylate. The reaction followed a free radical polymerization mechanism. The structure and properties of CM-St-g-P2CEtA were investigated by advanced analytical techniques. The CM-St-g-P2CEtA was employed for the remediation of Methylene Blue (MB) dye from wastewater. The removal percentage (%R) of MB was checked under different parameters, like different pH levels, different initial concentrations of dye, different adsorbent doses, and different contact times. The results obtained during the experiment were subjected to different adsorption and kinetic models. In the kinetic investigation, the experimental results were best represented by the pseudo-second-order kinetic model due to its high R2 value of 0.999. Similarly, with a regression coefficient (R2) value of 0.947, the Langmuir adsorption isotherm was best represented by the experimental results. The Langmuir adsorption model showed that MB dye was adsorbed on the surface of CM-St-g-P2CEtA in a monolayer pattern. The pseudo 2nd order kinetic model suggested that the adsorption process favored chemisorption mechanism. The CM-St-g-P2CEtA showed maximum percentage removal efficiency (%R) of 99.3% for MB dye.

A study on the role of surface functional groups of metakaolin in the removal of methylene blue: Characterization, kinetics, modeling and RSM optimization.

In this study, thermally activated kaolinite clay is explored as a suitable material for dye removal applications, which gave rise to highly reactive silica species in a broad range of aluminosilicate clusters. Multinuclear NMR studies described it as a short-range network in which Al sites in IV, V, and VI are coordinated, and Si is present mainly as Si(Q4(1Al)). Critical parameters for methylene blue (MB) were determined by the Placket Burman Design (PBD) as initial dye concentration, contact time, adsorbent dosage, pH and size. The % of MB removal studied after optimizing the parameters by central composite design (CCD), based on Response Surface Methodology, was found to be 90%. The adsorption kinetics and thermodynamics were systematically studied and reported by fitting them into different models. The maximum removal of the dye reached 97.8 mg/g according to the Freundlich isotherm, accomplished through chemisorption, following a pseudo-second-order reaction and the process is thermodynamically spontaneous and endothermic. The line spectrum of X-ray photoelectron spectroscopy (XPS) shows the participation of Si, Al, O, Ca and Na of Metakaolin (AK) and nitrogen of MB in the adsorption process. The appropriate stabilization of the N atom of the chromophore on the Si and Al atom in AK resulting from the ionic interaction on the surface is established from an increase in the binding energy of Al and Si. A single bridging oxygen signal at 532.32eVcorresponding to AK after dye adsorption tends to form siloanol/aluminol, and their interaction is lowered to 531.58eV. Regeneration of adsorbent after thermal treatment without loss of efficiency proved.

Effective decontamination of methylene blue from aqueous solutions using novel nano-magnetic biochar from green pea peels.

The conversion of agricultural waste into high-value carbon products has been an attractive area in waste management strategy. This study highlighted the synthesis and effectiveness of green pea peels (GPP), green pea biochar (GPBC), and nano-ferromagnetic green pea biochar (NFGPBC) by the ferrous/ferric co-precipitation synthesis method for eliminating cationic dyes molecules from solutions. The morphological, physicochemical, and structural properties of GPP, GPBC, and NFGPBC were approved by Scanning Electron Microscopy (SEM), Transmission Emission Microscopy (TEM), Energy Dispersive X-ray (EDX), Bruneau Emmett Teller (BET), Fourier Transform Infrared spectroscopy (FTIR), and X-ray Diffraction (XRD) techniques. Vibrating Sample Magnetometry (VSM) analysis confirmed the NFGPBC magnetization performance. The capacity of each adsorbent for methylene blue removal was evaluated at various parameters of material dosage (50-250 mg/150 mL), pH (2-12), initial concentration (50-250 mg/L), contact time (0-90 min) and temperature (20-60 °C). The three developed adsorbent materials GPP, GPBC, and NFGPBC, possessed reasonable BET surface areas of 0.6836, 372.54, and 147.88 m2g-1, and the corresponding monolayer adsorption capacities of 163.93, 217.40, and 175.44 mg/g, respectively. The superior performances of GPBC and NFGPBC were due to their increased surface area compared with the parent green pea peels (GPP). The results from adsorption kinetics studies of all prepared materials were pseudo-second-order and Elovich kinetics models. The thermodynamic parameters exhibited MB sorption's favorability, spontaneity, and endothermic nature. The NFGPBC material experienced Vander Waal forces, electrostatic interaction, hydrogen bonding, and hydrophobic interactions as predominant modes of the solid-liquid interaction. The regeneration, recycling, and reusability of the synthesized GPP, GPBC, and NFGPBC performed at five adsorption cycles revealed that NFGPBC demonstrated excellent cyclical performances attaining a minimum 8.9% loss in capacity due to paramagnetic properties. Thus, NFGPBC is a green, efficient, and eco-friendly material recommended for large-scale production and application in wastewater.

Hydrogel of HEMA, NVP, and Morpholine-Derivative Copolymer for Sulfate Ion Adsorption: Behaviors and Mechanisms.

SO42--containing compounds are widely present in wastewater generated from various industries and mining industries, such as slag leachate, pulp and paper wastewater, modified starch wastewater, etc. When the concentration of SO42- is too high, it will not only be corrosive to metal equipment but also accumulate in the environmental media. Based on this, a novel cationic hydrogel HNM was synthesized in this study by introducing morpholine groups into the conventional hydrogel HEMA-NVP system for the adsorption of SO42- in aqueous solutions. Characterizations by Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS) indicated that morpholine groups had been introduced into the as-synthesizedhydrogels. The scanning electron microscope (SEM) characterization results show that the introduction of morpholine groups changed the surface of the hydrogel from micron-scale wrinkles to nanoscale gaps, increasing the contact area with the solution. The results of static water contact angle (WCA), equilibrium water content (EWC), and SO42- adsorption capacity show that the introduction of morpholine groups not only further improved the equilibrium water content and hydrophilicity of the hydrogel but also greatly improved the SO42- adsorption capacity of the hydrogel, with the maximum SO42- adsorption amount of 21.59 mg/g, which was much higher than that of the hydrogel without morpholine groups of 5.15 mg/g. Further studies found that the adsorption of SO42- on the hydrogel HNM was pH-dependent, and acidic conditions were favorable for the adsorption. Therefore, the introduction of morpholine groups greatly enhanced the ability of conventional HEMA-NVP hydrogels to remove SO42- from aqueous solutions.

Photocatalytic Degradation Studies of Organic Dyes over Novel Cu/Ni Loaded Reduced Graphene Oxide Hybrid Nanocomposite: Adsorption, Kinetics and Thermodynamic Studies.

Nowadays, for environmental remediation, photocatalytic process involving graphene-based semiconductors is considered a very promising oxidation process for water treatment. In the present study, nanocomposite (Cu/Ni/rGO) has been synthesized by Dypsis lutescens leaf extract. Characterization of the sample was carried out by UV-visible spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Different parameters like contact time, nanocatalyst amount, dye concentration, effect of temperature. and pH factor were optimized to examine the maximum removal efficiency for dyes rhodamine B and alizarine R with and without visible light source. In both cases, i.e., with or without light, maximum removal was observed at 20 mg of nanocatalyst for 5 ppm concentration of both dyes at 45 °C temperature and pH 10 for rhodamine B and pH 4 for alizarine R, respectively with a 20 min contact time. Maximum removal of dyes 93% rhodamine B and 91% alizarine R were observed under a tungsten lamp as compared to without a tungsten lamp, i.e., 78% of RhB and 75% of AR from mixture solution of these dyes. To assess the rate of reaction, spontaneity, and nature of reaction thermodynamics, kinetics and adsorption isotherms were studied. Thermodynamic values indicated that both dyes depicted endothermic and spontaneous degradation processes. Isotherm data fitted best to a Freundlich isotherm, while results of kinetic studies of both dyes followed the pseudo 2nd order kinetic equation. In the end, scavenging radical studies concluded that hydroxyl radicals were the main active specie involved in the photocatalytic degradation process, and regeneration experiments resulted that Cu/Ni/rGO nanocomposites were re-utilized for about four times.

A Stable Fe-Zn Modified Sludge-Derived Biochar for Diuron Removal: Kinetics, Isotherms, Mechanism, and Practical Research.

To remove typical herbicide diuron effectively, a novel sludge-derived modified biochar (SDMBC600) was prepared using sludge-derived biochar (SDBC600) as raw material and Fe-Zn as an activator and modifier in this study. The physico-chemical properties of SDMBC600 and the adsorption behavior of diuron on the SDMBC600 were studied systematically. The adsorption mechanisms as well as practical applications of SDMBC600 were also investigated and examined. The results showed that the SDMBC600 was chemically loaded with Fe-Zn and SDMBC600 had a larger specific surface area (204 m2/g) and pore volume (0.0985 cm3/g). The adsorption of diuron on SDMBC600 followed pseudo-second-order kinetics and the Langmuir isotherm model, with a maximum diuron adsorption capacity of 17.7 mg/g. The biochar could maintain a good adsorption performance (8.88-12.9 mg/g) under wide water quality conditions, in the pH of 2-10 and with the presence of humic acid and six typical metallic ions of 0-20 mg/L. The adsorption mechanisms of SDMBC600 for diuron were found to include surface complexation, π-π binding, hydrogen bonding, as well as pore filling. Additionally, the SDMBC600 was tested to be very stable with very low Fe and Zn leaching concentration ≤0.203 mg/L in the wide pH range. In addition, the SDMBC600 could maintain a high adsorption capacity (99.6%) after four times of regeneration and therefore, SDMBC600 could have a promising application for diuron removal in water treatment.

Iron-rich coal fly ash-polydopamine-silver nanocomposite (IRCFA-PDA-Ag NPs): tailored material for remediation of methylene blue dye from aqueous solution.

Water pollution has become one of the most acute environmental problems. One of the pollutants coming to water bodies from industries are dyes, which are harmful to human health, living organisms, and the esthetic appearance of water. Most dyes are toxic, carcinogenic, rarely biodegradable, and highly soluble in water. Therefore, industrial wastewater treatment has become important. Adsorption technique of removal of dyes from water is simple, efficient, and inexpensive as compared to other techniques. Adsorption efficiency depends on the type and surface area of adsorbents. Iron-rich coal fly ash (IRCFA)-Polydopamine (PDA)@ Silver (Ag) nanocomposite was prepared by separating the iron-rich part (IRCFA) from coal fly ash and coated with polydopamine. IRCFA was mixed with 10 mM tris buffer solution containing 1 g dopamine. The prepared IRCFA-PDA was added to an aqueous solution of silver nitrate, heated at 60 °C, and then 30 mL of flower waste extract was added to this solution. Solid IRCFA-PDA@Ag was obtained, and the prepared nanocomposite was used for the removal of methylene blue (MB) dye from water. The nanocomposite used was prepared by a cost-effective method and has high reusability, separability, and fast regeneration ability. The mechanism of removal of MB dye has been discussed in detail.

Efficiency evaluation of titanium oxide nanocomposite membrane in adsorption of chromium from oil effluents.

Reverse osmosis and nanofiltration (NF) are the essential physical separation technologies used to remove contaminants from liquid streams. A hybrid of nanofiltration and forward osmosis (FO) was used to increase the removal efficiency of heavy metals in synthesized oil effluents. Thin-film nanocomposite (TFN) membranes were synthesized by applying surface polymerization on a polysulfone substrate to use in the forward osmosis process. The impact of different membrane fabrication conditions such as time, temperature, and pressure on effluent flux, the effect of different concentrations of the heavy metal solution on adsorption rate and sedimentation rate, the impact of TiO2 nanoparticles on the performance and structure of forward osmosis membranes were investigated. The morphology, composition, and properties of TiO2 nanocomposites made by the infrared spectrometer and X-ray diffraction (XRD) were studied. Kinetic modeling and Langmuir, Freundlich, and Tamkin relationships were used to draw adsorption isotherms and evaluate adsorption equilibrium data. The results indicated that pressure and temperature directly affect water outlet flux, and time affects it indirectly. Evaluating the isothermal relationships revealed that chromium adsorption from the TFN 0.05 ppm membrane and thin-film composite (TFC) membrane follows the Langmuir model with correlation coefficients of 0.996 and 0.995, respectively. The significant removal of heavy metals and the acceptable amount of water flux demonstrated the appropriate potential of the titanium oxide nanocomposite membrane, which can be used as an effective adsorbent to remove chromium from aqueous solutions.

Synthesizing nanoparticles of zinc and copper ferrites and examining their potential to remove various organic dyes through comparative studies of kinetics, isotherms, and thermodynamics.

Nanoparticles of zinc ferrite (ZnFe2O4) and copper ferrite (CuFe2O4) were synthesized, and characterized, and these materials were applied for removal of organic dyes of alizarin yellow R (AYR), thiazole yellow G (TYG), Congo red (CR), and methyl orange (MO) from industrial wastewater through adsorption technique. Synthesis of ZnFe2O4 and CuFe2O4 was achieved through chemical co-precipitation method. These nanomaterials were characterized for physicochemical properties using XRD, FTIR, BET, VSM, DLS, Zeta-potential, and FESEM-EDX analytical instruments. BET surface areas of ZnFe2O4 and CuFe2O4 were 85.88 m2/g and 41.81 m2/g, respectively. Adsorption-influencing parameters including effect of solution pH, adsorbent quantity, initial concentration of dye pollutant, and contact time were examined. Acidic medium of the solution favored higher percentage of removal of dyes in wastewater. Out of different isotherms, Langmuir equilibrium isotherm showed the best fit with experimental data, indicating monolayer adsorption in the treatment process. The maximum monolayer adsorption capacities were found as 54.58, 37.01, 29.81, and 26.83 mg/g with ZnFe2O4, and 46.38, 30.06, 21.94, and 20.83 mg/g with CuFe2O4 for AYR, TYG, CR, and MO dyes, respectively. From kinetics analysis of the results, it was inferred that pseudo-second-order kinetics were fitting well with better values of coefficient of determination (R2). The removal of four organic dyes from wastewater through adsorption technique using nanoparticles of ZnFe2O4 and CuFe2O4 was observed to be spontaneous and exothermic. From this experimental investigation, it has been inferred that magnetically separable ZnFe2O4 and CuFe2O4 could be a viable option in removal of organic dyes from industrial wastewater.

Effective removal of Pb(II) and Ni(II) ions by Bacillus cereus and Bacillus pumilus: An experimental and mechanistic approach.

Herein, we report a bacteria-based strategy as an efficient, reasonable, benign, and promising methodology for remediating heavy metals fed waterbodies. The contemporary study deals with isolating, screening, and characterizing heavy metal resistive bacteria from metal-rich sites. The transcriptome analysis reveals the identity of the isolated species as Bacillus pumilus and Bacillus cereus. Batch studies put forth the bioremoval results in designed conditions of different pH, concentration, dose, and time. The mechanistic actions are drawn using complementary techniques such as Scanning Electron Microscopy (SEM) and Fourier Transform Infrared Spectroscopy (FTIR). The theory of surface adsorption of lead (Pb(II)) and nickel (Ni(II)) is further fostered by the application of adsorption isotherms. The conducted studies establish the bacterial morphological stratagems and multifarious biochemical approaches for countering metallic ions of Pb(II) and Ni(II). The exhibition of significant removal results by the isolated bacterial strains in simulated water samples with remarkable proliferation rates has opened up its favorability for industrial platforms.

Sustainable removal of Cr(VI) using graphene oxide-zinc oxide nanohybrid: Adsorption kinetics, isotherms and thermodynamics.

Metal-based adsorbents are limited for hexavalent chromium [Cr(VI)] adsorption from aqueous solutions because of their low adsorption capacities and slow adsorption kinetics. In the present study, decorated zinc oxide (ZnO) nanoparticles (NPs) on graphene oxide (GO) nanoparticles were synthesized via the solvothermal process. The deposition of ZnO NPs on graphene oxide for the nanohybrid (ZnO-GO) improves Cr(VI) mobility in the nanocomposite or nanohybrid, thereby improving the Cr(VI) adsorption kinetics and removal capacity. Surface deposition of ZnO on graphene oxide was characterized through Fourie Transform Infra-red (FTIR), UV-Visible, X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive Spectroscopy (EDS), and Brunauer-Emmett-Teller (BET) techniques. These characterizations suggest the formation of ZnO-GO nanocomposite with a specific area of 32.95 m2/g and pore volume of 0.058 cm2/g. Batch adsorption analysis was carried to evaluate the influence of operational parameters, equilibrium isotherm, adsorption kinetics and thermodynamics. The removal efficiency of Cr(VI) increases with increasing time and adsorbent dosage. FTIR, FESEM and BET analysis before and after the adsorption studies suggest the obvious changes in the surface functionalization and morphology of the ZnO-GO nanocomposites. The removal efficiency increases from high-acidic to neutral pH and continues to decrease under alkaline conditions as well. Mathematical modeling validates that the adsorption follows Langmuir isotherm and fits well with the pseudo 2nd order kinetics (Type 5) model, indicating a homogeneous adsorption process. The thermodynamics study reveals that Cr(VI) adsorption on ZnO-GO is spontaneous, endothermic, and entropy-driven. A negative value of Gibb's Free Energy represents the thermodynamic spontaneity and feasibility of the sorption process. To the best of our knowledge, this is the first study of Cr(VI) removal from aqueous solution using this hybrid nanocomposite at near-neutral pH. The synthesized nanocomposites prove to be excellent candidates for Cr(VI) removal from water bodies and natural wastewater systems.

Elucidation the influence of design variables on coagulation-flocculation mechanisms in the lab-scale bio-coagulation on toxic industrial effluent treatment.

Bio-coagulants are environmentally friendly substances that have shown potential in removing organic and inorganic contaminants from wastewater from the Imitation Paint Industry. Under the optimized conditions, the use of the three bio-coagulants (of plant origin), Strychnos potatorum, Cactus opuntia and Portunus sanguinolentus (crab) shell (of animal origin) were evaluated, and their removal mechanism was based on kinetic models and adsorption isotherms. The error analysis method was used to find the best isotherm fit. In addition, the kinetic model parameters showed the absence of chemisorption and confirmed the existence of pore diffusion. The interaction between coagulant and pollutant, the type, homogeneity and intensity of the coagulation process, the pollutant absorption capacity of the coagulant were evaluated with the aid of the adsorption isotherm models. From the Pseudo first-order kinetic model an equilibrium pollutant uptake (mg/g) was marked as 598, 554 and 597 for Strychnos potatorum, Cactus opuntia and Portunus sanguinolentus respectively. The better affinity between the pollutants and the bio coagulants were observed through the lower values of Langmuir isotherm constant kL. The adsorption intensity from Freundlich model (nF) were ranged between 1 and 10 for all the listed coagulants, which revealed the physisorption behavior and heterogeneous mechanism of removal. With these results, it would be possible to conduct scale-up studies to adopt the process for practical systems.

Bioremediation potential of Dicentrarchus labrax fish scales for dye-based emerging contaminants by ANN-GA hybrid modeling.

This work investigates the possibility of using scales of sea bass Dicentrarchus labrax as a low-cost material for the adsorptive removal of methylene blue (MB) cationic dye in aqueous solutions. The physical-chemical characterizations of fish scales in natura (FS-in natura) revealed through thermogravimetry that they are composed of inorganic (hydroxyapatite) and organic (collagen) phases in relatively similar amounts. Spectroscopy analyses show that the interactions of MB with FS-in natura occur mainly in the organic phase layer of the adsorbent. The effects of initial MB concentration (5.0 × 10-4 and 5.0 × 10-3 mol L-1) and temperature (25-55 °C) on the adsorption efficiency of FS-in natura were evaluated. FS-in natura at MB concentration (5.0 × 10-3 and 5.0 × 10-4 mol L-1) exhibited the maximum adsorption capacities of 2.2 × 10-3 mol g-1 at 25 °C and 2.8 × 10-5 mol g-1 at 55 °C, respectively. The pseudo-second-order model represented the adsorption kinetics well, and the equilibrium isotherm data were better correlated using the Langmuir equation. The newly developed neural model demonstrated a high predictive capacity with an R-value greater than 0.99 and reduced values for mean squared error, root mean squared error, and mean absolute error equal to 0.003, 0.055, and 0.0348, respectively. The genetic algorithm was used to optimize the experimental conditions of the process. In conclusion, the sea bass scales have promising prospects as a low-cost alternative material for removing cationic dyes from aqueous solutions.

Macro-Reticular Ion Exchange Resins for Recovery of Direct Dyes from Spent Dyeing and Soaping Liquors.

Dyes are a major class of organic pollutants that are well-known for their harmful impact on aquatic life and humans. Several new strategies for removing colours from industrial and residential effluents have recently emerged, with adsorption being the best option. The current study looked at the recovery of direct dyes from aqueous streams for reuse using macro-reticular ion exchange resins (IERs). The investigation includes dyeing single jersey cotton grey textiles with direct dyes from the Isma dye Company in Kafr El Dawar, Egypt. After centrifuging and separating the supernatant liquid, solutions from thirteen different dyes, produced at an average concentration between the wasted and soaping liquor concentrations, were calculated spectrophotometrically from the first dyeing trials. Kinetic data were well fitted with pseudo-second-order rate kinetics. The amounts of dye retained by the anion exchangers increased with a rise in temperature in the case of Strong Base Resin (SBR) and vice versa for Weak Base Resin (WBR). Batch adsorption experiments with SBR and WBR were conducted for each dye, and both Freundlich and Langmuir isotherms were constructed. It was found that adsorption obeyed both isotherms, that monolayer adsorption took place, and that the dye molecular weight, structure, and solubility, as well as the type of anionic resin used, had varying effects on the extent of absorption. The monolayer sorption capacities Q0 determined from the Langmuir isotherm model for the strongly and weakly basic anion exchangers were found to be 537.6 and 692 mg/g for Direct Yellow RL, respectively. As a result, Yellow RL exhibited the greatest adsorption on both SBR and WBR. Orange GRLL, Blue 3B, and Congo Red, on the other hand, were the poorest colours absorbed by the IERs, whereas Blue RL demonstrated good adsorption by SBR and accelerated adsorption by WBR. Most of the dyes may be recovered and reused in this manner.

Impact of the variety on the adsorption of anthocyanins and tannins on grape flesh cell walls.

BACKGROUND: During winemaking, after extraction from the skins, anthocyanins and tannins adsorb onto the pulp flesh cell walls. The present study aimed to quantify the amounts adsorbed and their impact on wine composition, the impact of variety and ethanol on adsorption, and whether the presence of anthocyanins plays a role and impacts tannin adsorption. RESULTS: Anthocyanin and tannin fractions obtained by mimicking winemaking conditions were mixed with fresh flesh cell walls of two varieties: Carignan and Grenache. Adsorption isotherms were measured. Adsorption of tannins was higher with Carignan than with Grenache and decreased when the ethanol content increased. In comparison, anthocyanins were adsorbed in small amounts, and their mixing with tannins had no impact on their adsorption. The differences were related to differences in pulp cell wall composition, particularly in terms of extensins and arabinans. CONCLUSION: Adsorption of tannins, which can reach 50% of the initial amount, depends on the pulp cell wall composition. This needs to be investigated further. © 2021 Society of Chemical Industry.