Removal Of Chromium Research Articles

Chromium adsorption efficiency by functional polymeric nanocomposite membrane: A case study for environmental sustainability

AbstractWe have designed and developed nonwoven fabric supported electrospun polymeric nanofibrous‐based membrane for robust filtration system for ecological sustainability of clean water. The fabricated nanocomposites filters were tested for the removal of chromium (VI) toxic heavy metal ions from contaminated feedstock water. The interpenetrating network like morphological structure obtained from pure and composite nanofibers‐based membranes have been thoroughly investigated to understand the structure–properties of highly entangled system. It has been found that incorporating functional moieties onto nanocomposite membranes significantly impacts the absorption efficiency of toxic metals. The pore sizes of the hierarchical geometries have been varied to insight into its impact on flow rate and efficiency of filtration. The strategy of interfacing the multifunctional composite polyethylene terephthalate nanofiber membrane supported on nonwoven fabric to generate heterostructures has found to provide mechanically stable platform for efficient metal ion removal. It has been found by BET surface area analysis that the nanofibers reinforced with functional nanomaterials has controlled pore geometry compared to pristine PET electrospun nanofibers which lead to higher absorption of metal ions. We have highlighted the importance of mechanically stable electrospun polymeric nanofibers membrane‐based mitigation strategies to meet the huge demand of potable water for long‐term environmental sustainability.Highlights Mechanically toughened freestanding nanofibers mat supported on nonwoven fabric. Functionally upgrade nanofibers by incorporation of carbon based nanofillers. Controlled porosity by morphological optimization for removal of contaminates.

Synergistic effects of sulfur vacancies and internal electric fields in FeS/MoS2 heterojunctions: A new approach to photocatalytic chromium removal

Molybdenum disulfide (MoS2) is heralded as an exemplary two-dimensional (2D) functional material, largely attributed to its distinctive layered structure. Upon forming heterojunctions with reducing species, MoS2 displays remarkable photocatalytic properties. In this research, we fabricated a novel heterojunction photocatalyst, FeS/MoS2-0.05, through the integration of FeS with hollow MoS2. This composite aims at the efficient photocatalytic reduction of hexavalent chromium (Cr(VI)). A comprehensive array of characterization techniques unveiled that MoS2 flakes, dispersed on FeS, provide numerous active sites for photocatalysis at the heterojunction interface. The inclusion of FeS seemingly promotes the formation of sulfur vacancies on MoS2. Consequently, this heterojunction catalyst exhibits photocatalytic activity surpassing pristine MoS2 by a factor of 3.77. The augmented activity of the FeS/MoS2-0.05 catalyst is attributed chiefly to an internal electric field at the interface. This field enhances the facilitation of charge transfer and separation significantly. Density functional theory (DFT) calculations, coupled with experimental analyses, corroborate this observation. Additionally, DFT calculations indicate that sulfur vacancies act as pivotal sites for Cr(VI) adsorption. Significantly, the adsorption energy of Cr(VI) species shows enhanced favorability under acidic conditions. Our results suggest that the FeS/MoS2-0.05 heterojunction photocatalyst presents substantial potential for the remediation of Cr(VI)-contaminated wastewater.

Synthesis of eco-friendly polyaniline-zeolite nanocomposite for pollutant remediation: Empowered by robust machine learning algorithm

The present research assesses the synthesis of an eco-friendly polyaniline and zeolite 4A (4 Armstrong) nanocomposite for enhanced adsorption of dye and heavy metal. Zeolite has been synthesized utilizing natural Kutch-sourced Kaolin clay. The materials synthesized were characterized via various instrumental techniques which confirms the formation of the desired materials. The composite exhibits superior performance in removing hazardous pollutants, demonstrating the removal of 98.5 % chromium in 12 min and 99.8% Congo red in 50 min, individually. Furthermore, for simultaneous removal, the composite continued displaying remarkable performance having a removal rate of 99% and 98.5 % for Congo red and chromium, respectively within 50 min, only. The nanocomposite follows the Freundlich isotherm model for chromium removal indicating physisorption and the Langmuir isotherm model for Congo removal signifying chemisorption. Artificial intelligence and machine learning (ML) techniques have been employed on the data set for the simulation of the adsorption percentage of the synthesized adsorbent. Various uncharted data visualizing techniques, including scatter plots, correlation coefficients, and mutual information were applied to explain the correlation between experimental variables. Conventional regression techniques showed poor performance with a high mean squared error (MSE) of 23 and an R2 value of 0.89. However, Bayesian optimization assisted ML model significantly improved the results. The Gaussian process with a polynomial function was the best performer, achieving an R2 value of 0.99 and mean squared error of 0.008. This research highlights the novel synthesis and effectiveness of the adsorbent materials, demonstrating the potential of machine learning in environmental remediation.

Experimental Investigation of Tannery wastewater by Electrocoagulation method

Abstract Treating tannery wastewater poses a significant challenge due to its composition, comprising biogenic materials from hides and a diverse range of organic and inorganic chemicals. Experimental procedures were conducted using an electrochemical reactor employing sacrificial electrodes—mild steel as both anode and cathode—in a unceasing process. Numerous working parameters such as current density and electrolysis duration were examined to achieve optimal reduction in presence of turbidity, total solids, COD, BOD, TDS, and Chromium content. Enhanced reductions in COD, BOD, TDS, and chromium content were observed at higher flow rates. The applied current density also notably impacted the reduction efficiency of COD, BOD, TDS, and chromium content. Investigation into the electro coagulation method employing short cell current (1A) and solvable mild steel electrodes revealed their efficacy compared to aluminium electrodes, particularly in chromium removal, achieving over 90% removal efficiency. However, the use of mild steel electrodes resulted in the formation of a black precipitate characteristic of iron (II) sulphides during the treatment, although effectively reducing effluent coloration. The removal efficiency of chloride, however, remained lower, at less than 12%. A comprehensive discussion on the mechanisms involved in the removal of COD, chromium, total dissolved salts, total solids, chloride and coloration using soluble mild steel electrodes was presented. The predominant role of the electrode was highlighted by treating tannery wastewater with mild steel electrodes, followed by filtration, resulting in removal rates of 68.0% for chemical oxygen demand, 43.1% for chromium, 55.1% for total dissolved salts and 84.3% for coloration, considering initial concentrations of 2850 mg/L, 230 mg/L, 100 mg/L, 100 mg/L, and a 256- fold dilution, respectively.

Development of biochar using herbal industry waste for removal of hexavalent chromium from aqueous solution: Column study

Biochar is an rich source of carbon formed through biomas’s thermal decomposition. There is a lot of scope of interest in developing biochar derived from biomass in various disciplines to address the most significant ecological challenges. In the present study herbal waste collected from herbal processing industry (Bangalore, India). So, this biomass will be no use after the extraction process. Hence, present work mainly concentrates the conversion this herbal waste to biochar (BC). Research highlights the BC was prepared from herbal industry waste using pyrolysis method. The obtained BC used as adsorbent for adsorption of Cr (VI) from aqueous solution. A characterization of BC was performed using XRD, SEM-EDS and FT-IR which confirms the material. The adsorption experiments were carried out using batch and fixed bed column. The experimental studies were carried out at room temperature with initial Cr (VI) concentrations (IC) of 10–120 ppm using an adsorbent dosage (AD) of 0.05–0.55 g, agitation speed of 150 rpm for contact time (CT) 15–165 min and temperature (20–40 °C). Then various parameters for column study like bed height, flow rate and IC were also studied. The maximum removal of Cr (VI) was 88 % found at a pH 2, AD 0.55g, CT 90 min, and IC 100 ppm at 30 °C. For column study: higher removal of Cr (VI) achieved by bed height (BH) of 6 cm and at lower flow rate (FR), of 3 mL/min.

Development of a continuous electrochemical reactor incorporated with waste-derived activated carbon electrode for the effective removal of hexavalent chromium from industrial effluent.

Being a recognized carcinogen, hexavalent chromium is hazardous to both human and environmental health. Thus, it is imperative to regulate and oversee their levels in a variety of industries, including textiles, dyes, pigments, and metal finishing. This study strives to reduce Cr(VI) in wastewater by using capacitive deionization in conjunction with an activated carbon-based electrode and a continuous electrochemical reactor (CER). Activated carbon derived from rubberwood sawdust demonstrated excellent properties, including a high surface area of 1157 m2g-1. The electrical conductivity and mechanical stability of the electrode were enhanced by the incorporation of synthesized expanded graphite (EG) into the AC. Key parameters were optimized via systematic batch electroreduction experiments with an optimal response surface design. The efficacy of the fabricated CER was proved when it successfully reduced Cr(VI) in a 5mg L-1 solution within 15min under optimized conditions, in contrast to the considerably longer durations anticipated by conventional methods. Validation of these findings was done by treating industrial wastewater of 30mg L-1 in the CER. The electroreduction of Cr(VI) followed the Langmuir isotherm with a maximum capacity of 13.491mgg-1 and pseudo-second-order kinetics. These results indicate that the combined use of the modified AC electrode and CER holds potential as a sustainable and economical approach to effectively eliminate Cr(VI) from wastewater.

Radiation reduction modification of sp2 carbon-conjugated covalent organic frameworks for enhanced photocatalytic chromium(VI) removal

A sp2 carbon-conjugated covalent organic framework (BDATN) was modified through γ-ray radiation reduction and subsequent acidification with hydrochloric acid to yield a novel functional COF (named rBDATN-HCl) for Cr(VI) removal. The morphology and structure of rBDATN-HCl were analyzed and identified by SEM, FTIR, XRD and solid-state 13C NMR. It is found that the active functional groups, such as hydroxyl and amide, were introduced into BDATN after radiation reduction and acidification. The prepared rBDATN-HCl demonstrates a photocatalytic reduction removal rate of Cr(VI) above 99% after 60 min of illumination with a solid-liquid ratio of 0.5 mg/mL, showing outstanding performance, which is attributed to the increase of dispersibility and adsorption sites of rBDATN-HCl. In comparison to the cBDATN-HCl synthesized with chemical reduction, rBDATN-HCl exhibits a better photoreduction performance for Cr(VI), demonstrating the advantages of radiation preparation of rBDATN-HCl. It is expected that more functionalized sp2 carbon-conjugated COFs could be obtained by this radiation-induced reduction strategy.

Chromium (VI) removal by magnetite nanoparticles immobilized with extracellular polymeric substances extracted from Lysinibacillus sp. WH.

Magnetite nanoparticles (nano-Fe3O4) and nano-Fe3O4 immobilized with bacterial extracellular polymeric substances (EPSs) extracted from Lysinibacillus sp. WH (Fe3O4/bact) were comparatively studied for the removal of Cr (VI) ions from aqueous solution in batch study. The objectives were to explore the removal of Cr (VI) efficiency by nano-Fe3O4 and Fe3O4/bact under varying bacterial concentrations at a range of acidic pH. Results indicated that 150 ppm Cr (VI) could be effectively removed by 5 g/L of nano-Fe3O4 at pH 4, with the efficiency of 89.2 ± 12%. The equilibrium time, determined by a pseudo-second-order model (R2 = 0.9983), was after 5 h, indicating chemical adsorption. The Cr (VI) removal by the nano-Fe3O4 immobilized with bacterial EPS was effective and steady under a wide range of acidic conditions although bacterial EPS has an alkaline nature. Here, we are the first to demonstrate that Cr (VI) removal efficiency by different concentrations of EPS was not significantly different, suggesting EPS concentration is possibly not the most crucial factor to be optimized for Cr (VI) removal in the future. This study shows the potential application of nano-Fe3O4 immobilized with bacterial EPS for wastewater treatment. PRACTITIONER POINTS: The equilibrium time for magnetite nanoparticles to remove Cr (VI) is 5 h, suggesting chemical adsorption. The Cr (VI) removal efficiency of either magnetite nanoparticles or bacterial EPS is stable under a wide range of acidic conditions. Magnetite nanoparticles immobilized with bacterial EPS extracted from Lysinibacillus sp. WH has a potential application for Cr (VI) removal in wastewater.

Harnessing the chromium reduction potential of Pseudomonas aeruginosa JRHM33: A comprehensive study on bioinformatics, phenotype microarray, and CCD-RSM optimization

Large amounts of wastewater are generated due to overpopulation and industrialization, The bioavailability, toxicity, and permanence of metals make heavy metal contamination a big environmental hazard. In order to maximize chromium (Cr+6) removal efficiency, the current investigation was carried out from industrial wastewater using Pseudomonas aeruginosa JRHM33.35 bacterial strains were discovered based on their physical, and biochemical properties and resistance towards chromium (Cr+6) heavy metal. The most significant bacterial strain JRHM33 found the highest-level of 1000 mg/L of chromium (Cr+6) resistance. The bacterial strain JRHM33, which has 99 % similarity to Pseudomonas aeruginosa, was found using 16 S rRNA sequencing and is employed in subsequent steps. Sequencing and study of conserved domains indicate that JRHM33 contains the laccase gene and belongs to the multicopper oxidase superfamily, which is known for its ability to reduce metal ions. Analysing phenotype microarray (PM) technology sheds light on Pseudomonas aeruginosa JRHM33 metabolic profile of microbial cells. Additionally, a series of process parameter optimizations were tried using the central composite design of response surface methodology (CCD-RSM) in an effort to reduce the amount of chromium (Cr+6) in the effluent as much as possible. At 6.8 pH, 90 min of incubation, inoculum size is 3.8 ml, and agitation is 104 rpm, a maximum 71 % Cr+6 reduction was attained. The model constructed has an R2 score of 0.983 indicates a very statistically significant outcome from the analysis of variance. The experimental outcomes and the predicted results were remarkably similar, according to the validation experiment. Studies have revealed that bacterial strains obtained from effluent containing high levels of metals utilize their inherent capability to change harmful heavy metals into less dangerous or harmless forms.

Intercalation of GO-Ag nanoparticles in cellulose acetate nanofiltration mixed matrix membrane for efficient removal of chromium and cobalt ions from wastewater

Cellulose acetate (CA)/Polyethylene glycol (PEG) blended composite nanofiltration (NF) membrane encompassing graphene oxide-silver (GO-Ag) nanoparticles (NPs) has been successfully synthesized by dissolution casting techniques. The effect of different NP loadings on membrane morphology, surface roughness, hydrophilicity surface charge and permeation flux were evaluated. Owing to Donnon exclusion, steric hindrance, and solution diffusion mechanism, the synthesized modified membranes exhibited excellent rejection rates in the order of Co (II) (99 %) > Cr (VI) (91 %). Furthermore, pure water flux (PWF) of the modified membrane was obtained 660.56 L/m2h which is 78.45 % greater than pristine membrane. Due to its high surface hydrophilicity, surface roughness, and porosity, modified membrane exhibited good antifouling characteristics. The results indicated that the intercalation of GO-Ag NPs with a loading ratio of 0.8 wt% leads to the optimum membrane for Cr (VI) and Co (II) removal. The present work demonstrates the potential application of GO-Ag/CA modified NF mixed matrix membrane for serving as a promising platform for eliminating heavy metal ions in wastewater.

Recent Development in Nanoparticle-Assisted Microbial Fuel Cell for Enhanced Reduction of Chromium.

Chromium metal is a potential toxin released by various industries as by products. Reduction of the same costs an ample amount of manpower and wealth. Alternate, economical, efficient, and sustainable form of chromium reduction while generating electricity is a boon that microbial fuel cell (MFC) has provided to man. It paves way for an attractive technique to process hazardous elements. Nature as well as the type of electrode modulates the efficiency of reduction and power production. Many previously published studies have reviewed chromium removal from effluents as well as through MFCs, but utilization of nanoparticle-based MFC for chromium removal has not been exclusively done before. Hence, the objective of the current review is to provide exclusive study on nanoparticle-assisted MFC for chromium reduction. Reputed published data from the past 5years have been studied meticulously to compare the best outcomes of MFC in chromium removal. Chromium is found to be removed mostly in double-chambered MFC with a maximum removal of 100% when iron is used as an electrode. Removal of the same has led to generation of maximum power of 1965.4 mW m-2 when palladium nanoparticles are used at the electrode. Removal rates of Cr(VI) from a mixture of NiCo2O4, MoS2, and graphite felt in a dual-chamber MFC showed an 8.13% increase after 24h of light exposure. Another efficient setup used MoS2 nanosheets and Alpha-FeOOH nanoparticles in a dual-chamber MFC to completely remove Cr(VI) and achieve a high removal ratio of 91.45%. The current study reviews the recent updates in chromium reduction through MFC and its significance in future as a potential instrument for bioremediation and energy source.

Macroporous lignin adsorbents: A bio-sourced tool kit to defuse the Cr(VI) threat in wastewater

Amino-functionalised (triethylenetetramine) macroporous lignin monoliths were produced by curing an emulsion template containing untreated kraft black liquor with oxirane-crosslinkers. These lignin-based adsorbents were tested for the removal of Cr(VI) from water and synthetic waste water. A one-pot rout for their production is presented and their chemical and physical nature was investigated. Produced monoliths were tested in static and continuous adsorption experiments and chromium removal from water and synthetic wastewater was quantified via UV–vis spectroscopy. The nitrogen content of functionalised lignin monoliths reached up to 5.1 wt%, leading to adsorption capacities of up to 897 mg/g at pH = 2, as compared to non-functionalised lignin monoliths with a maximum adsorption capacity of 117 mg/g. The adsorption capacity of lignin monoliths produced is amongst the highest of bio-based materials presented in the literature.

Effective removal of chromium, copper, and nickel heavy metal ions from industrial electroplating wastewater by in situ oxidative adsorption using sodium hypochlorite as oxidant and sodium trititanate nanorod as adsorbent

Sodium hypochlorite and synthesized sodium trititanate nanorods (Na2Ti3O7, 186 × 1270 nm) were used as the oxidant and adsorbents for in situ oxidative adsorption treatment of actual electroplating wastewaters containing Cr(VI) (2.6‒5.2 mg∙L‒1), Cu2+ (2.7‒5.4 mg∙L‒1), and Ni2+ (0.2705‒0.541 mg∙L‒1) ions at pH of 8.8‒9.1 and 20‒60 °C. The as-synthesized sodium trititanate nanorods were characterized by XRD, HRTEM, N2 adsorption/desorption, SEM, EDX, and Zeta potential techniques. The concentrations of heavy metal ions in wastewaters were analyzed by ICP technique. After in situ oxidative adsorption treatment under the concentrations of 25 g∙L‒1 for sodium hypochlorite and 125 mg∙L‒1 for sodium trititanate nanorods at 60 °C for 5 h, the heavy metal ion concentrations could be reduced from initial value of 2.6 to final value of 1.92 mg∙L‒1 for Cr(VI), 3.6 to 0.17 mg∙L‒1 for Cu2+, and from 0.2705 to 0.097 mg∙L‒1 for Ni2+, respectively. Cr(VI), Cu2+, and Ni2+ ions could be effectively removed by the in situ oxidative adsorption method. The in situ oxidative adsorption processes of Cr(VI), Cu2+, and Ni2+ ions are satisfactorily simulated by the pseudo-second order adsorption kinetics and Langmuir adsorption isotherm, respectively. Adsorption thermodynamics analyses reveal that the oxidative adsorption processes of Cr(VI), Cu2+, and Ni2+ ions are spontaneous and endothermic. The oxidation degree of metal-contained complexes influences the values of thermodynamics functions.

Research and Application of Gangue for the Preparation of Polymerized Aluminum Magnesium Chloride Flocculant

Polymerized aluminum magnesium chloride (PAMC) flocculant was prepared from gangue as a raw material, and the effects of pH, the polymerization time, and the polymerization temperature on the performance of the PAMC were investigated by a one-factor test, based on which, orthogonal experiments (three-factor and two-level) were conducted to optimize the relevant parameters. Meanwhile, FTIR and SEM were used to characterize the polymerized aluminum magnesium chloride, and the sample was applied in printing and dyeing wastewater treatment. The results showed that a pH value of 2.2 and a reaction at 60 °C for 4.5 h were the optimal preparation conditions; the characterization analysis showed that the synthesized product was polymerized aluminum magnesium chloride; the turbidity removal rate of the PAMC for printing and dyeing wastewater was increased by 2.1%, the COD removal rate was increased by 3.1%, the ammonia nitrogen removal rate was increased by 2.1%, and the chromaticity removal rate was increased by 9.2% compared with that of PAC.

Efficient removal of chromate from wastewater using a one-pot synthesis of chitosan cross-linked ceria incorporated hydrous copper oxide bio-polymeric composite

Remediating hexavalent chromium [Cr(VI)] from contaminated water systems is a significant concern due to its harmful effects on human health, aquatic life, and plants. To tackle this issue, scientists have created a chitosan cross-linked hydrous ceria incorporated cupric oxide bio-polymeric composite (CHCCO) by combining chitosan biopolymer with corresponding metal ions using glutaraldehyde as a cross-linker. The composite was characterized using advanced analytical instruments such as FTIR, p-XRD, SEM, XPS, etc. The synthesized composite (CHCCO) was then tested for its efficiency in removing Cr(VI) from synthetic Cr(VI) aqueous samples. The parameters examined included pH, material dose, contact time, concentration, temperature, and co-existing ions. The experimental data showed that the kinetics and equilibrium data fit well with the pseudo-second-order and the Freundlich isotherm models, respectively. Thermodynamic analysis demonstrated that the investigated surface adsorption process is spontaneous and endothermic. Except for the SO42− ion, no other species imparts adverse influence significantly on the reaction. The CHCCO bio-composite surfaces were refreshed using a dilute NaOH (1.0 M) solution and effectively recycled five times for Cr(VI) adsorption, indicating no significant surface activity deterioration. This study highlights the high effectiveness of CHCCO bio-polymeric composites in Cr(VI) remediation and the potential for this technology as an easy-to-use technique for environmental restoration.

Mechanical Enhancement and Water Treatment Efficiency of Nanocomposite PES Membranes: A Study on Akçay Dam Water Filtration Application.

Polymeric membranes are widely used in water treatment because of their ease of fabrication and low cost. The flux and purification performance of membranes can be significantly improved by incorporating appropriate amounts of nanomaterials into the polymeric membrane matrices. In this study, neat poly(ether sulfone) (PES), PES/nano copper oxide (CuO), and PES/nano zinc oxide (ZnO) membranes are fabricated via phase inversion. The pure water flux of the neat PES membrane, which is 355.14 L/m2·h, is increased significantly with the addition of nano-CuO and nano-ZnO, and the pure water fluxes of the nanocomposite membranes vary in the range of 392.65-429.74 L/m2·h. Moreover, nano CuO and nano ZnO-doped PES nanocomposite membranes exhibit higher conductivity, color, total organic carbon, boron, iron, selenium, barium, and total chromium removal efficiencies than neat PES membranes. The membrane surfaces examined by Scanning Electron Microscopy (SEM) after water filtration revealed that those containing 0.5% wt. nano CuO and nano ZnO are more resistant to fouling than the membrane surfaces containing 1% wt. nano CuO and nano ZnO. Based on the results of this study, 0.5% wt. nano ZnO-doped PES membrane is found to be the most suitable membrane for use in water treatment due to its high pure water flux (427.14 L/m2·h), high pollutant removal efficiency, and high fouling resistance. When the mechanical properties of the membranes are examined, the addition of CuO and ZnO nanoparticles increases the membrane stiffness and modulus of elasticity. The addition of 0.5% and 1% for CuO leads to an increase in the modulus of elasticity by 57.95% and 324.43%, respectively, while the addition of 0.5% and 1% for ZnO leads to an increase in the modulus of elasticity by 480.68% and 1802.43%, respectively. At the same time, the tensile strength of the membranes also increases with the addition of nanomaterials.

Simulation of hexavalent chromium removal by electrocoagulation using iron anode in flow-through reactor

An electrocoagulation (EC) model is developed for hexavalent chromium reduction and precipitation, using iron electrodes. Parallel removal mechanisms such as adsorption of chromium on ferrihydrite and direct reduction at the cathode is assumed negligible due to low concentration of Cr(VI). The reaction model presented for batch system represents species complexation, precipitation/dissolution, acid/base, and oxidation-reduction reactions. Batch reactor simulation is verified using experimental data obtained by Sarahney et al. (2012), where the effect of initial chromium concentration, pH, volumetric current density, and ionic strength is considered (Sarahney et al., 2012). The model couples multicomponent ionic transport in MATLAB with chemical reaction model in PHREEQC, as a widely used computational programming tool and a geochemical reaction simulator with comprehensive geochemistry databases. The suggested current density is 0.05−0.3mA/cm2 and the surface to volume ratio in batch reactor is considered 0.017 1/cm. Design parameters are presented for operation of a flow-through hexavalent chromium removal using electrocoagulation by iron electrode to treat Cr(VI) in range of 10–50 mg/L. The operational parameters for a flow-through EC reactor for Cr(VI) removal is suggested to follow 0.05mA/cm2≤3nFeQcCrVIinlet≤0.3mA/cm2.

Effective removal of chromium by adsorption using Delonix regia bark derived activated carbon from aqueous solution: a sustainable approach.

This study introduces a new biosorbent derived from Delonix regia bark-activated carbon to efficiently remove Chromium Cr(VI) metal ions from aqueous systems. The biosorbent was synthesized from the bark powder of the plant species and chemically activated with phosphoric acid. The biosorbent was characterized using FTIR, SEM, and BET to determine its functional properties and structural morphology. The batch adsorption experiments examined the optimal conditions for Cr(VI) metal ion adsorption, identifying that the highest removal efficiency occurred at pH levels of 2. The ideal adsorbent dosage was determined to be 2.5g/L, with equilibrium achieved at a contact time of 60min at the optimal temperature of about 303K for a Cr(VI) metal ion concentration of 20mg/L. Various isotherm models were applied to the adsorption equilibrium values, revealing that the adsorbent had a maximum removal capacity of approximately 224.8mg/g for Cr(VI) metal ions. The adsorption process of Cr(VI) on the DAC biosorbent was best described by the Freundlich isotherm, indicating multilayer adsorption. The kinetic data fit well with the pseudo-second-order model. Thermodynamic parameters suggested that the adsorption process was spontaneous, exothermic, and feasible across different temperatures. Furthermore, the desorption studies showed that the DAC biosorbent can easily be rejuvenated and utilized several cycles with high adsorption capacity. These findings indicate that the developed adsorbent is environmentally friendly and effective for removing Cr(VI) from water systems.

Production of activated carbon from spent coffee grounds (SCG) for removal of hexavalent chromium from synthetic wastewater solutions

In this research, spent coffee grounds (SCG) are converted into a highly valuable porous adsorbent which removes chromium (VI) from wastewater with high efficiency. A set of nine Spent Coffee Ground Activated Carbon (SCG-AC) adsorbent samples were synthesized, by varying key parameters including pyrolysis temperature (400, 600 °C), pyrolysis duration (1 and 2 h), and the impregnation ratio of the activating agent, KOH (ranging from 0:1 to 2:1). Characterizations of these adsorbent samples were conducted by advanced analytical tools including SEM, EDX, XRD, FTIR, TGA, and BET. Furthermore, we carried out adsorption studies, exploring the effects of temperature and dosage variations. Additionally, point zero charge experiments and desorption studies were carried out to further understand the adsorption process. The outcomes of our investigation demonstrate the successful synthesis of these spent coffee ground-derived adsorbents, with a yield of up to 34%. Notably, these adsorbents exhibited high efficiency in extracting chromium (VI) from water, with removal efficiencies ranging from 75% to 100%. The adsorption isotherms revealed the Langmuir model to be the most fitting descriptor of the adsorption behavior. Moreover, a thermodynamics study revealed the process to be endothermic in nature which furthers our understanding of the underlying mechanisms. Importantly, our cost assessment shows the economic advantage of the synthesized adsorbent over commercial counterparts such as zeolite, making it a competitive choice for real-world applications. In summation, the study not only introduces an innovative and sustainable utilization of spent coffee grounds but also delivers an in-depth exploration of the synthesized adsorbent's ability in chromium (VI) removal. Our holistic approach, encompassing thorough experimentation, characterization, and economic evaluation, solidifies the significance of this research in tackling environmental concerns and propelling advancements in wastewater treatment methodologies.

Utilization of thermally treated sludge for the removal of hexavalent chromium from drainage wastewater: a laboratory and field study

Utilization of thermally treated sludge for the removal of hexavalent chromium from drainage wastewater: a laboratory and field study