Regeneration of exhausted adsorbents after PFAS adsorption: A critical review.

The adsorption process efficiently removes per- and polyfluoroalkyl substances (PFAS) from water, but managing exhausted adsorbents presents notable environmental and economic challenges. Conventional disposal methods, such as incineration, may reintroduce PFAS into the environment. Therefore, advanced regeneration techniques are imperative to prevent leaching during disposal and enhance sustainability and cost-effectiveness. This review critically evaluates thermal and chemical regeneration approaches for PFAS-laden adsorbents, elucidating their operational mechanisms, the influence of water quality parameters, and their inherent advantages and limitations. Thermal regeneration achieves notable desorption efficiencies, reaching up to 99% for activated carbon. However, it requires significant energy input and risks compromising the adsorbent's structural integrity, resulting in considerable mass loss (10-20%). In contrast, chemical regeneration presents a diverse efficiency landscape across different regenerants, including water, acidic/basic, salt, solvent, and multi-component solutions. Multi-component solutions demonstrate superior efficiency (>90%) compared to solvent-based solutions (12.50%), which, in turn, outperform salt (2.34%), acidic/basic (1.17%), and water (0.40%) regenerants. This hierarchical effectiveness underscores the nuanced nature of chemical regeneration, significantly influenced by factors such as regenerant composition, the molecular structure of PFAS, and the presence of organic co-contaminants. Exploring the conditional efficacy of thermal and chemical regeneration methods underscores the imperative of strategic selection based on specific types of PFAS and material properties. By emphasizing the limitations and potential of particular regeneration schemes and advocating for future research directions, such as exploring persulfate activation treatments, this review aims to catalyze the development of more effective regeneration processes. The ultimate goal is to ensure water quality and public health protection through environmentally sound solutions for PFAS remediation efforts.

Adsorption of Cu(II) and Ni(II) from Aqueous Solutions Using Synthesized Alkali-Activated Foamed Zeolite Adsorbent: Isotherm, Kinetic, and Regeneration Study.

Water pollution, particularly from heavy metals, poses a significant threat to global health, necessitating efficient and environmentally friendly removal methods. This study introduces novel zeolite-based adsorbents, specifically alkali-activated foamed zeolite (AAFZ), for the effective adsorption of Cu(II) and Ni(II) ions from aqueous solutions. The adsorbents' capabilities were comprehensively characterized through kinetic and isotherm analyses. Alkaline activation induced changes in chemical composition and crystalline structure, as observed via XRF and XRD analyses. AAFZ exhibited a significantly larger pore volume (1.29 times), higher Si/Al ratio (1.15 times), and lower crystallinity compared to ZZ50, thus demonstrating substantially higher adsorption capacity for Cu(II) and Ni(II) compared to ZZ50. The maximum monolayer adsorption capacities of ZZ50 and AAFZ for Cu(II) were determined to be 69.28 mg/g and 99.54 mg/g, respectively. In the case of Ni(II), the maximum monolayer adsorption capacities for ZZ50 and AAFZ were observed at 48.53 mg/g and 88.99 mg/g, respectively. For both adsorbents, the optimum pH for adsorption of Cu(II) and Ni(II) was found to be 5 and 6, respectively. Equilibrium was reached around 120 min, and the pseudo-second-order kinetics accurately depicted the chemisorption process. The Langmuir isotherm model effectively described monolayer adsorption for both adsorbents. Furthermore, the regeneration experiment demonstrated that AAFZ could be regenerated for a minimum of two cycles using hydrochloric acid (HCl). These findings highlight the potential of the developed adsorbents as promising tools for effective and practical adsorption applications.

Impact of polystyrene microplastics on the growth and photosynthetic efficiency of diatom Chaetoceros neogracile.

The increasing prevalence of microplastic pollution in aquatic environments has raised concerns about its impact on marine life. Among the different types of microplastics, polystyrene microplastics (PSMPs) are one of the most commonly detected in aquatic systems. Chaetoceros neogracile (diatom) is an essential part of the marine food web and plays a critical role in nutrient cycling. This study aimed to monitor the ecotoxicological impact of PSMPs on diatoms and observe enzymatic interactions through molecular docking simulations. Results showed that diatom growth decreased with increasing concentrations and exposure time to PSMPs, and the lowest photosynthetic efficiency (Fv/Fm) value was observed after 72 and 96 h of exposure to 200 mg L-1 of PSMPs. High concentrations of PSMPs led to a decrease in chlorophyll a content (up to 64.4%) and protein content (up to 35.5%). Molecular docking simulations revealed potential interactions between PSMPs and the extrinsic protein in photosystem II protein of diatoms, suggesting a strong affinity between the two. These findings indicate a detrimental effect of PSMPs on the growth and photosynthetic efficiency of diatoms and highlight the need for further research on the impact of microplastics on marine microbial processes.

Corrosion by Polythionic Acid in the Oil and Gas Sector: A Brief Overview.

Polythionic acid (PTA) corrosion is a significant challenge in the refinery industry, leading to equipment degradation, safety risks, and costly maintenance. This paper comprehensively investigates the origin, progression, mechanism, and impact of PTA corrosion on various components within refinery operations. Special attention is afforded to the susceptibility of austenitic stainless steels and nickel-based alloys to PTA corrosion and the key factors influencing its occurrence. Practical strategies and methods for mitigating and preventing PTA corrosion are also explored. This paper underscores the importance of understanding PTA corrosion and implementing proactive measures to safeguard the integrity and efficiency of refinery infrastructure.

Effect of Aluminosilicates' Particle Size Distribution on the Microstructural and Mechanical Properties of Metakaolinite-Based Geopolymers.

The present study focused on investigating the differences in properties between calcined and milled aluminosilicates with different particle size distributions. Two types of clay, i.e., kaolin and kaolinitic claystone, were subjected to calcination at 750 °C, and subsequent milling to obtain different fractions with distinct particle size distributions. These fractions were then combined with a potassium alkaline activator and quartz sand in a 50:50 weight ratio to form a geopolymer composite. The geopolymer binders were then characterized using a mercury intrusion porosimeter (MIP), scanning electron microscopy (SEM), and a rotary rheometer. Mechanical tests were conducted on the geopolymer composites prepared from aluminosilicates with varying particle size distributions. The findings indicated that aluminosilicates with a finer particle size distribution exhibited higher levels of dissolved aluminum (10,000 mg/kg) compared to samples with coarser particle size distributions (1000 mg/kg). Additionally, as the particle size distribution decreased, the dynamic viscosity of the geopolymer binders increased, while the average pore size decreased. Finally, the mechanical properties of the geopolymer composites derived from both tested aluminosilicates demonstrated a decline in performance as the mean particle size increased beyond 10 µm.

Post-synthetic thiol modification of covalent organic frameworks for mercury(II) removal from water.

Various materials have been developed for environmental remediation of mercury ion pollution. Among these materials, covalent organic frameworks (COFs) can efficiently adsorb Hg(II) from water. Herein, two thiol-modified COFs (COF-S-SH and COF-OH-SH) were prepared, through the reaction between 2,5-divinylterephthalaldehyde and 1,3,5-tris-(4-aminophenyl)benzene, followed by post-synthetic modification using bis(2-mercaptoethyl) sulfide and dithiothreitol, respectively. The modified COFs showed excellent Hg(II) adsorption abilities with maximum adsorption capacities of 586.3 and 535.5 mg g-1 for COF-S-SH and COF-OH-SH, respectively. The prepared materials showed excellent selective absorbability for Hg(II) against multiple cationic metals in water. Unexpectedly, the experimental data showed that both co-existing toxic anionic diclofenac sodium (DCF) and Hg(II) performed positive effect for capturing another pollutant by these two modified COFs. Thus, a synergistic adsorption mechanism between Hg(II) and DCF on COFs was proposed. Moreover, density functional theory calculations revealed that synergistic adsorption occurred between Hg(II) and DCF, which resulted in a significant reduction in the adsorption system's energy. This work highlights a new direction for application of COFs to simultaneous removal of heavy metals and co-existing organic pollutants from water.

Toxicity Effects of Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) on Two Green Microalgae Species.

Amongst per- and polyfluoroalkyl substances (PFAS) compounds, perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) have a high persistence in physicochemical and biological degradation; therefore, the accumulation of PFOS and PFOA can negatively affect aquatic organisms and human health. In this study, two microalgae species (Chlorella vulgaris and Scenedesmus obliquus) were exposed to different concentrations of a PFOS and PFOA mixture (0 to 10 mg L-1). With increases in the contact time (days) and the PFAS concentration (mg L-1) from 1 to 7, and 0.5 to 10, respectively, the cell viability, total chlorophyll content, and protein content decreased, and the decrease in these parameters was significantly greater in Scenedesmus obliquus. As another step in the study, the response surface methodology (RSM) was used to optimize the toxicity effects of PFAS on microalgae in a logical way, as demonstrated by the high R2 (>0.9). In another stage, a molecular docking study was performed to monitor the interaction of PFOS and PFOA with the microalgae, considering hydrolysis and the enzymes involved in oxidation-reduction reactions using individual enzymes. The analysis was conducted on carboxypeptidase in Chlorella vulgaris and on c-terminal processing protease and oxidized cytochrome c6 in Scenedesmus obliquus. For the enzyme activity, the affinity and dimensions of ligands-binding sites and ligand-binding energy were estimated in each case.

Intercalating negatively charged pillars into graphene oxide sheets to enhance sulfonamide pharmaceutical removal from water.

Herein, novel composite materials were prepared by intercalating functional pillars, i.e., pentafluorobenzene (PFB) and sodium 2,3,4,5,6-pentafluorobenzoate (PFBS), into graphene oxide (GO) sheets. It led to forming size hives and increased availability of intrinsic area of GO. The synthesized materials (GO-PFB and GO-PFBS) were investigated as adsorbents to eliminate sulfadiazine (SD) from aqueous solutions. The adsorption capacities of GO-PFBS (1002.21 µmol/g) and GO-PFB (564.17 µmol/g) were 6.37 and 3.59 times higher than that of GO (157.21 µmol/g), respectively. The adsorption of SD onto GO-PFBS decreased with increasing solution pH. Density functional theory (DFT) results revealed that the SD adsorption onto the adsorbents was exothermic, and the introduction of the carboxylate groups showed lower binding energy. It was found that hydrophobic interaction fully participates in the adsorption process, and the electrostatic complementation of hydrogen bonding further enhances the SD adsorption. Obtained results showed that intercalating functional rigid molecules as pillars to support GO sheets could improve its adsorption behavior.

Improved fractal kinetic model to predict mechanochemical destruction rate of organic pollutants.

Mechanochemical destruction of organic pollutants by high energy milling with inorganic reagents is considered a promising non-thermal technology to detoxify hazardous waste. However, due to complex nature of the physicochemical phenomena involved, pollutant destruction kinetics heavily depends on the used reagents and operating parameters, thus varying case by case. In the present work, a fractal model was validated as flexible tool to interpolate pollutant mechanochemical destruction data satisfactorily. In addition, such model was expanded to estimate the contributions of the inorganic reagent and the pollutant to the overall reaction rate. Specifically, the kinetic constant associated to mechanical activation of the co-milling reagent and that related to pollutant destruction reaction were calculated. Their values resulted to depend only on the specific compound, hence, the tabulated data could be used to predict the pollutant mechanochemical degradation rate for any kind of mixture.

Preparation of magnetic powdered carbon/nano-Fe3O4 composite for efficient adsorption and degradation of trichloropropyl phosphate from water.

Trichloropropyl phosphate (TCPP) as a widely used typical chlorinated organophosphate flame retardant has received significant attention because of its widespread presence in water and negative effects on human health. In this study, a ball-milling method was used to prepare a magnetic powdered carbon adsorbent (PC/nano-Fe3O4 composite) for TCPP removal via adsorption and catalytic degradation. The effect of Fe3O4 content on TCPP adsorption and degradation performance by PC/nano-Fe3O4 composite was investigated. The PC/nano-Fe3O4 composite prepared by high Fe3O4 content (25%) was not favorable for TCPP adsorption and degradation. However, the PC/Fe3O4 containing low Fe3O4 content (10%) had insufficient magnetic separation ability from water. The synthesized PC/nano-Fe3O4 composite with a Fe3O4/PC mass ratio of 1/5 exhibited a maximum adsorption capacity of 2682.1 µg/g as well as a complete TCPP degradation within 3 h in a Fenton-like system. Moreover, the possible break sites of TCPP and its degradation pathway were proposed based on theoretical calculation and experimental analysis. Regeneration studies showed that PC/nano-Fe3O4 composite had high reusability and adsorption capacity in six cycles, while its catalytic performance declined in the multiple reuse cycles. This strategy could be extended to prepare other magnetic powdered adsorbents for organic pollutant adsorption and degradation.

Modelling of hydrogen sulfide fate and emissions in extended aeration sewage treatment plant using TOXCHEM simulations.

Odors due to the emission of hydrogen sulfide (H2S) have been a concern in the sewage treatment plants over the last decades. H2S fate and emissions from extended aeration activated sludge (EAAS) system in Muharram Aisha-sewage treatment plant (MA-STP) were studied using TOXCHEM model. Sensitivity analysis at different aeration flowrate, H2S loading rate, wastewater pH, wastewater temperature and wind speed were studied. The predicted data were validated against actual results, where all the data were validated within the limits, and the statistical evaluation of normalized mean square error (NMSE), geometric variance (VG), and correlation coefficient (R) were close to the ideal fit. The results showed that the major processes occurring in the system were degradation and emission. During summer (27 °C) and winter (12 °C), about 25 and 23%, 1 and 2%, 2 and 2%, and 72 and 73% were fated as emitted to air, discharged with effluent, sorbed to sludge, and biodegraded, respectively. At summer and winter, the total emitted concentrations of H2S were 6.403 and 5.614 ppm, respectively. The sensitivity results indicated that aeration flowrate, H2S loading rate and wastewater pH highly influenced the emission and degradation of H2S processes compared to wastewater temperature and wind speed. To conclude, TOXCHEM model successfully predicted the H2S fate and emissions in EAAS system.

Removal performance and optimisation of pharmaceutical micropollutants from synthetic domestic wastewater by hybrid treatment.

Occurrence of pharmaceutical micropollutants in aquatic environments has been one amongst serious environmental problems. During this study, two reactors, including a sequencing batch reactor (SBR) + powdered composite adsorbent (CA) (first reactor, SBR + CA) and a sequencing batch reactor (second reactor, SBR), were designed to treat synthetic wastewater. Powdered CA was added with a dosage of 4.8 g L-1 to the first reactor. Tap water was contaminated with chemical oxygen demand (COD), ammonia and three pharmaceuticals, namely, atenolol (ATN), ciprofloxacin (CIP) and diazepam (DIA) to produce synthetic wastewater. The SBR + CA illustrated a better performance during synthetic municipal wastewater treatment. Up to 138.6 mg L-1 (92.4%) of COD and up to 114.2 mg L-1 (95.2%) of ammonia were removed by the first reactor. Moreover, optimisation of pharmaceuticals removal was conducted through response surface methodology (RSM) and artificial neural network (ANN). Based on the RSM, the best elimination of ATN (90.2%, 2.26 mg L-1), CIP (94.0%, 2.35 mg L-1) and DIA (95.5%, 2.39 mg L-1) was detected at the optimum initial concentration of MPs (2.51 mg L-1) and the contact time (15.8 h). In addition, ANN represented a high R2 value (>0.99) and a rational mean squared error (<1.0) during the optimisation of micropollutants removal by both reactors. Moreover, adsorption isotherm study showed that the Freundlich isotherm could justify the abatement of micropollutants by using CA better than the Langmuir isotherm.

Computational investigation of N2O adsorption and dissociation on the silicon-embedded graphene catalyst: A density functional theory perspective.

One of the encouraging processes to protect the environment is the catalytic conversion of N2O and other harmful greenhouse gases. Employing heteroatom dopants into the Graphene structure for this conversion is an attractive technique owing to its relatively low price and the very low destructive impacts. DFT was applied to explore fundamental and principal reactions of N2O adsorption and dissociation over the Silicon-embedded Graphene catalyst to contribute to the search for green catalysts in the conversion of toxic gases into less harmful ones. Forming a surface peroxy group O22-, N2O bond cleavage and oxygen atom transfer were theoretically investigated. It is found that the N2O molecule requires +0.52, +0.88 and + 0.4 eV of activation energies through mentioned three reactions, respectively, to adsorb and decompose to N2 and O2. The parallel, lying-atop-011 and flat were stable forms with adsorption energies of -0.20 (-4.65), -0.19 (-4.53) and -0.18 (-4.46) and -0.19 eV (-4.53 kcal/mol), respectively. The achieved outcomes reveal that Silicon-embedded Graphene has a high potential to be used as a more efficient and green catalyst for the catalytic conversion of the air polluting gases in comparison to the Selenium-doped Graphene, Fe+, Manganese-embedded Graphene and Magnesium oxide (MgO) catalysts.

Pesticides in aquatic environments and their removal by adsorption methods.

Although pesticides are widely used in agriculture, industry and households, they pose a risk to human health and ecosystems. Based on target organisms, the main types of pesticides are herbicides, insecticides and fungicides, of which herbicides accounted for 46% of the total pesticide usage worldwide. The movement of pesticides into water bodies occurs through run-off, spray drift, leaching, and sub-surface drainage, all of which have negative impacts on aquatic environments and humans. We sought to define the critical factors affecting the fluxes of contaminants into receiving waters. We also aimed to specify the feasibility of using sorbents to remove pesticides from waterways. In Karun River in Iran (1.21 × 105 ng/L), pesticide concentrations are above regulatory limits. The concentration of pesticides in fish can reach 26.1 × 103 µg/kg, specifically methoxychlor herbicide in Perca fluviatilis in Lithuania. During the last years, research has focused on elimination of organic pollutants, such as pesticides, from aqueous solution. Pesticide adsorption onto low-cost materials can effectively remediate contaminated waters. In particular, nanoparticle adsorbents and carbon-based adsorbents exhibit high performance (nearly 100%) in removing pesticides from water bodies.

Effect of high energy ball milling on organic pollutant adsorption properties of chitosan.

In the present work, chitosan physicochemical transformations that occur during high energy ball milling are investigated and correlated with adsorption capacity of organic pollutants (using azo-dye reactive red 2 as molecular probe). Experimental results reveal that chitosan ball milled for 1 h shows a 70% increase of adsorption capacity, compared to unmilled one, while longer milling time causes a sensible reduction of such capacity. This trend correlates with specific surface area evolution under milling, thus suggesting the primary role of particle comminution in augmenting chitosan adsorption properties. Amorphization of particle surface was found to be marginally relevant for adsorption capacity enhancement. Maximum adsorption capacity (estimated by isothermal equilibrium study) and adsorption rate are augmented by ball milling, with an optimal value found at 1 h milling. Finally, the milled materials were tested to adsorb perfluorooctane sulfonate, obtaining 1.54 mmol g-1 uptake with 1 h milled chitosan. This suggests that chitosan could be used as a cheap expendable material to remove those pollutants, like perfluorooctane sulfonate and the other perfluoroalkyl substances, that deserves destruction and cannot be removed by conventional degradation technologies.

Technologies for the nitrogen oxides reduction from flue gas: A review.

The required energy of the global industry is mostly generated from fossil fuel sources, such as natural gas, gasoline, diesel, oil, and coal. Nitrogen oxides are one of the main air pollutants that are produced from the combustion of fossil fuels in stationary and mobile sources. Development of new technologies to decrease the NOx emission from exhaust gases is essential due to the harmful effect of NOx on the environment and human health. Compared with pre-combustion and combustion methods (with <50% NOx removal efficiency), the post-combustion methods with higher efficiency (above 80%) have attracted more attention in NOx elimination. This review describes the currently used technologies of NOx abatement. Different available post-combustion methods of NOx removal, including selective catalytic reduction (using different types of reducing reagents, including ammonia, hydrogen, hydrocarbons, and carbon monoxide), selective noncatalytic reduction, wet scrubbing, adsorption, electron beam, nonthermal plasma, and electrochemical reduction of NOx, are discussed.

Ultrasound-Assisted Preparation of Chitosan/Nano-Activated Carbon Composite Beads Aminated with (3-Aminopropyl)Triethoxysilane for Adsorption of Acetaminophen from Aqueous Solutions.

A composite chitosan/nano-activated carbon (CS-NAC) aminated by (3-aminopropyl)triethoxysilane (APTES) was prepared in the form of beads and applied for the removal of acetaminophen from aqueous solutions. NAC and APTES concentrations were optimized to obtain a suitable adsorbent structure for enhanced removal of the pharmaceutical. The aminated adsorbent (CS-NAC-APTES beads) prepared with 40% w/w NAC and 2% v/v APTES showed higher adsorption capacity (407.83 mg/g) than CS-NAC beads (278.4 mg/g). Brunauer-Emmett-Teller (BET) analysis demonstrated that the surface area of the CS-NAC-APTES beads was larger than that of CS-NAC beads (1.16 times). The adsorption process was well fitted by the Freundlich model (R2 > 0.95), suggesting a multilayer adsorption. The kinetic study also substantiated that the pseudo-second-order model (R2 > 0.98) was in better agreement with the experimental data. Finally, it was proved that the prepared beads can be recycled (by washing with NaOH solution) at least 5 times before detectable performance loss.

Simulation and computer modeling of asphaltene in different solvents on oil-water interfaces using a molecular dynamic methodology.

Molecular dynamics (MD) simulations were used to study the thermodynamic properties of asphalt binder components, namely asphaltene, and other solvents, such as pentane or toluene, before and after adding pentane or toluene. The two systems were compared by MD simulation under lots of molecules, temperature and pressure to predict their internal energy, structure, and density as a function of time or distance between molecules. Then the simulation results of the two systems were analyzed and compared to determine the influence of different solvents on asphaltene aggregation behavior. The results show that the asphaltenes with pentane or toluene in the two systems have different structure and dynamic characteristics and will produce different precipitation and aggregation characteristics. The aggregation behavior of asphaltene at water - oil interface with or without pentane or toluene was studied. The relationship between the molecular structure and the aggregation of asphaltene in different solvents was investigated.

Cross-linked chitosan/zeolite as a fixed-bed column for organic micropollutants removal from aqueous solution, optimization with RSM and artificial neural network.

Organic micropollutants (MPs) in low concentrations can affect aquatic ecosystems and human health. Adsorption technique is one of the promising methods to remove MPs. Chitosan and zeolites are environmentally friendly and low-cost adsorbents. Thus, removal of organic MPs (such as bisphenol A (BPA), carbamazepine (CBZ), ketoprofen (KTF) and tonalide (TND) from aqueous solution via cross-linked chitosan/zeolite, as a fixed-bed column, was investigated in the current study. Hydraulic retention time was set at 0.8 h pH and concentration of organic MPs ranged from 4 to 8 and 0.50 mg/L to 2.0 mg/L, and they were considered as factors in optimizing the removal of pollutants via response surface methodology (RSM). Approximately 1.4560 mg/L (89.0%) of BPA, 1.4724 mg/L (90.0%) of CBZ, 1.4920 mg/L (91.2%) of KTF and 1.4118 mg/L (86.3%) of TND were removed at 5.1 pH and 1.636 mg/L initial concentration as the optimum removal efficiency on the basis of RSM. Artificial neural network (ANN) was used to optimise removal effectiveness for each MP. The high R2 values and reasonable mean squared errors indicated that ANN optimized MP removal in a logical aspect. Adsorption isotherm studies revealed that organic MP removal through chitosan/zeolite could be explained with Freundlich and Langmuir isotherms.

Preparation of aminated cross-linked chitosan beads for efficient adsorption of hexavalent chromium.

Novel chitosan-based adsorbent (CS-DEO-SP) was successfully prepared by cross-linking and amination using diepoxyoctane (DEO) and spermine (SP) sequentially for the enhanced adsorption of Cr(VI) from aqueous solutions. The optimal CS-DEO-SP beads were prepared with 1.5 mg/L of SP for 5 h at 50 °C. The prepared beads exhibited heterogeneous and porous surfaces. The increased surface area (79.6%), pore volume (86.0%), and pore size (31.2%) of the modified adsorbent evidenced the successful modification of chitosan beads. The adsorption kinetics of Cr(VI) ions onto the prepared CS-DEO-SP beads was well fitted by the pseudo-second-order model (R2 > 0.97), and the adsorption isotherms adapted well with the Freundlich model (R2 > 0.96). The experimental data revealed that the adsorption of Cr(VI) ions on the CS-DEO-SP beads was extremely dependent on solution pH, and the maximum adsorption capacity of 358.1 mg/g was achieved at acidic condition (pH 2.0). After the regeneration of spent CS-DEO-SP beads using 1.0 mol/L NaOH, the adsorption capacity of reused adsorbent gradually declined within five consecutive adsorption cycles. Overall, the prepared CS-DEO-SP beads showed excellent stability in acidic solution and Cr(V) adsorption performance and thus can be used as an efficient adsorbent for eliminating Cr(VI) ions from acidic metal-plating wastewater.