Copper Adsorption Research Articles

Theoretical Study on Copper Adsorption on Zinc Oxide Surfaces

The study of copper on zinc oxide surfaces is a topic of ongoing research due to the importance of copper as a promoter in the low-temperature synthesis of methanol, the water-gas shift process and methanol steam reforming. The role of zinc oxide in supporting the stabilisation of the copper atoms and promoting the CO2 hydrogenation reaction is multifaceted and involves a range of physical and chemical factors. In this work, we used density functional theory (DFT) calculations to investigate the copper adsorption on zinc oxide surfaces on different sites. Bader charge analysis, adsorption energy and phonon inelastic neutron scattering (INS) associated with most stable systems were calculated and compared with previous theoretical and experimental results. We found that atomic copper adsorption on hollow site of ZnO(111) is the most stable and favourable site for copper adsorption compared to other zinc oxide surfaces. This is due to the strong metal-oxygen interaction between copper and the zinc oxide surface. We concluded that further studies are needed to investigate the catalytic activity of this catalyst under realistic reaction conditions with realistic models of copper supported on zinc oxide.

Adsorption of Copper and Chromium Mixed Solution on N-Doped Biomass-Activated Carbon

N-doped biomass activated carbon was prepared by direct ultrasonic method and redox method. Scanning electron microscopy, energy-dispersive spectroscopy, Brunnauer-Emmett-Teller, X-ray photoelectron spectroscopy, Zeta potential test, and other characterization methods were used to observe the pore structure, surface functional groups, elemental composition and distribution, and surface charged properties of the two samples. The adsorption experiment of Cu(II)/Cr(VI) mixed solution of two samples was carried out, and the influence of pH value, temperature, and concentration on material properties was explored. The results show that the equilibrium time, adsorption rate, and adsorption capacity of Cu(II)/Cr(VI) mixed solution are shorter, faster, and three times larger compared with the adsorption of single Cu(II) solution. The co-adsorption of Cu(ii) and Cr(vi) was observed. The adsorption capacity of Cr(vi) is not affected by the properties of the materials themselves, but increases with the increase of the initial concentration of Cu(II). The adsorption performance of activated carbon modified by redox method is better than that modified by direct ultrasonic method when adsorbing mixed solution of copper and chromium ions.

Selective adsorption of copper by amidoxime modified low-temperature biochar: Performance and mechanism.

Biochars prepared at 300-700°C were functionalized with amidoxime groups to evaluate their selective adsorptive removal capabilities towards Cu(II), Cd(II), and Pb(II). The results show that the amidoxime modification significantly enhanced the the Cu(II) adsorption capacity of the biochar prepared at 300°C (AOBC300) by 1.6 times, reaching 0.61mmol/g. In binary and ternary heavy metal solutions, AOBC300 exhibited preferential adsorption of Cu(II), followed by Pb(II) and Cd(II). High salinity, alkaline earth metal ions, humic substances, and other metal cations had minimal interference on the adsorption of heavy metals by AOBC300. Sample characterization revealed that amidoxime modification reduced the zeta potential and increased the hydrophilicity of the biochar. XPS analysis demonstrated that both N and O atoms of the amidoxime group are involved in the adsorption process, contributing to AOBC300's strong affinity for heavy metal ions. DFT calculations further confirmed the adsorption preference of different heavy metals on AOBC300. This study demonstrates that amidoxime grafting is an effective protocol for refining low-temperature biochar, aimed at efficiently eliminating heavy metals from waste streams.

Extraction of heavy metal ions from aqueous solutions by frame sorbents based on benzene-1,3,5-tricarboxylate (MBTC) and benzene-1,4-dicarboxylates (MB DC) of various metals

Pollution of soils and water sources with heavy metals leads to negative consequences for the environment associated with disruption of ecosystem balance, harm to the health of living organisms and humans. To solve this problem, organometallic frame sorbents capable of efficiently extracting heavy metal ions from aqueous solutions have been synthesized. During the conducted research, the regularities of the adsorption of cadmium, lead, copper, cobalt and nickel ions were studied using synthesized frame sorbents based on benzene-1,3,5-tricarboxylates (MBTC) and benzene-1,4-dicarboxylates (MBDC). The identification analysis performed on diffractograms of CoBTC and NiBTC powders showed the presence of structures [Co3(BTC)2·12H2O] and [Ni3(BTC)2·12H2O]. Unlike NiBTC, NiBDC dicarboxylate crystallizes in triclinic syngony (spatial group P1¯, Z = 1) and corresponds to the crystal structure [Ni3(OH)2(BDC)2··4H2O], the sample of the CuBTC compound crystallizes in cubic symmetry with the space group Fm3¯m (Z = 16) and corresponds to the crystal structure [Cu3(BTC)2·3H2O], and the CuBDC compound has a structure belonging to the monoclinic symmetry. The results of the analysis of isotherms of low-temperature nitrogen adsorption using synthesized MOFs made it possible to determine important textural characteristics of sorbents. It was noted that a strong adsorbate-adsorbent interaction is realized for CoBTC in the micropore region. It is shown that the specific surface area of synthesized sorbents, calculated by the Brunnauer-Emmett-Teller (BET) method, varies widely. Thus, for CoBTC and NiBTC compounds, it was 276.0 and 9.0 m2/g, respectively. The noted differences are due to the presence of a large number of micropores in the sorbent CoBTC. In most cases, the kinetic patterns of the adsorption of heavy metal ions can be described by a pseudo-second-order equation. The only example of the process proceeding according to the kinetic equation of the pseudo-first order is the adsorption of copper ions on the NiBDC sorbent. It is noted that cobalt, nickel and copper ions are better absorbed by sorbents containing the corresponding ions of the same name according to the Paneta-Faience rule. The linear relationship found between the sorption capacity and the logarithm of the ratio of the radius of ions to their electronegativity implies that the mechanism of adsorption of metal ions on MOFs is determined by the physicochemical properties of the ions themselves. The developed organometallic frame compounds can be effectively used in technologies for purification of water resources from toxic heavy metal ions.

Preparation of Magnetic Hemicellulosic Composite Microspheres and Adsorption of Copper Ions.

In this study, the fabrication of magnetic hemicellulosic composite microspheres and the adsorption of copper ions are explored. The microspheres were prepared by the micro-emulsion technique, using Fe3O4 nanoparticles and hemicellulose extracted from wheat straw with the ionic liquid B[mim]Cl as a solvent. Fe3O4 nanoparticles, synthesized through coprecipitation, were evenly encapsulated within the hemicellulosic microspheres. The Fe3O4 nanoparticles measured 10-15 nm in size, while the microspheres had an average diameter of about 20 μm and displayed a saturation magnetization of 35.95 emu/g. The optimal conditions for copper adsorption by the microspheres were found to be a pH of 5.0, a temperature of 323 K, and an initial copper ion concentration of 80 mg/L, resulting in an adsorption capacity of 85.65 mg/g after 24 h. The adsorption kinetics followed a pseudo-second-order model, and the Langmuir isotherm suggested a monomolecular layer adsorption mechanism, with a theoretical maximum capacity of 149.25 mg/g. In summary, the magnetic hemicellulosic microspheres exhibited considerable adsorption potential and favorable recycling capabilities for copper ions.

Adsorption of Copper, Zinc, Chromium and Nickel Using Plantation crop waste as Adsorbents in Contaminated Soil

This study investigates the adsorption behaviour of copper, zinc, chromium and nickel on plantation crops such as Arecanut husk (AH) and Coconut husk (CH) using a batch technique. Key parameters affecting the adsorption phenomenon were contact time, initial metal ion concentration, and temperature. The results showedequilibrium was reached within four hours, with adsorption capacity being temperature-dependent and endothermic. Efficiency of removal was maximumat lower concentrations, while adsorption capacity improved at higher concentration. Freundlich and Langmuir modelsareappropriatefor predicting the adsorption isotherm. At 300C, the maximum adsorption ofCu, Zn, Cr and Ni on AH and CH were 0.95 mg/g,1.27 mg/g, 0.78mg/g, 0.88 mg/g, 1.22mg/g, 1.64mg/g, 1.66mg/g, and 1.69 mg/g respectively. CH exhibited higher removal and adsorption capacities than AH, with zinc showing the strongest adsorption attraction, following the order Cu < Ni < Cr< Zn for plantation croptypes of adsorbents.

Modulated electronic properties of borophene nanoribbons using copper and oxygen atoms

The electronic and optical properties of borophene nanoribbons, influenced by the adsorption of copper (Cu) and oxygen (O) atoms in various configurations, were studied using first-principles calculations. The findings indicated that the most stable configuration, with the minimum adsorption energy of −9.09 eV, was achieved with double-upper center adsorbed double O atoms. By varying the adsorption positions and the number of Cu and O atoms, borophene nanoribbons were successfully tuned to transform into direct and indirect band-gap semiconductors. In particular, borophene nanoribbons with single and double-upper center adsorbed Cu atoms exhibited direct band gaps of 0.083 eV and 0.185 eV, respectively. In contrast, the double-upper center adsorbed double O atoms configuration resulted in an indirect band gap of 0.039 eV. The results further demonstrated that the Fermi levels crossed into the valence band, displaying p-type degenerate semiconductor characteristics for configurations with single and double-upper center adsorbed Cu atoms as well as double-upper center adsorbed double O atoms.

Enhancing kaolin performance through organic molecule modification and assessing its efficiency for lead and copper adsorption

The research aimed to enhance the efficacy of kaolin in water treatment by incorporating diphenylamine (DPA) and to evaluate its effectiveness in adsorbing lead and copper in wastewater in comparison to natural kaolin (Nat-kaolin). This entailed modifying kaolin with DPA to create DPA-kaolin and conducting comprehensive characterization utilizing a range of techniques, including X-ray diffraction analysis (XRD), scanning electron microscope (SEM), energy dispersion X-ray (EDX), thermogravimetric analysis (TGA), differential thermal analysis (DTA), Fourier-transform infrared spectroscopy (FTIR), and Brunauer-Emmett-Teller (BET) analysis. The results demonstrated the successful modification of DPA, as evidenced by an increase in BET-specific surface area of about 25 % (from 66.69 m².g−1 to 71.35 m².g−1), indicating enhanced adsorption capacity. XRD analysis confirmed the composition of the samples, while TGA/DTA indicated changes in water adsorption and dehydroxylation. SEM and EDX illustrated the tubular nature of the clay with a decrease in the amount of Al, about 10.76 %, and the amount of Si, about 10.38 %, on the DPA-kaolin. Notably, the FTIR spectrum of DPA-kaolin showed the presence of new vibration bands at 1248 cm−1, indicating the presence of DPA. In terms of adsorption, the DPA-kaolin exhibited significantly higher maximum adsorption capacities for Pb(II) and Cu(II) compared to the nat-kaolin, with values of 151 µmol/g and 134 µmol/g, respectively.These values were significantly higher than those observed for Nat-kaolin, which demonstrated adsorption capacities of 103 µmol/g for Pb(II) and 91 µmol/g for Cu(II). The adsorption kinetics indicated that the pseudo-second-order kinetic model described the sorption mechanism for both Pb(II) and Cu(II). This was evidenced by the values of R², which were 0.999 and 0.996, respectively. The study provides clear evidence that DPA-kaolin is more effective than Nat-kaolin in removing lead (Pb(II)) and copper (Cu(II)) from wastewater. Through rigorous experimentation, it was observed that DPA-kaolin exhibited notably enhanced adsorption capabilities for both Pb(II) and Cu(II) compared to Nat-kaolin. These findings serve to emphasize the practical importance and potential utility of the modification, offering promising prospects for the development of more efficient wastewater treatment methodologies.

Comprehensive study on copper adsorption using an innovative graphene carbonate sand composite adsorbent: Batch, fixed-bed columns, and CFD modeling insights

This study focused on an innovative graphene carbonate sand composite adsorbent, synthesized from carbonated porous sand and sucrose as raw materials, for the removal of copper ions via the adsorption process. The characteristics of this adsorbent are determined through comprehensive experiments and numerical simulations in batch and fixed-bed column conditions, which has not been extensively explored. Extensive experimentation demonstrated a remarkable 100 % removal efficiency under optimal conditions, which included a copper ion concentration of 3 g/L, a contact time of 10 h, and an adsorbent dosage of 35 g/L. The adsorption kinetics and isotherm results exhibited that the Elovich model (R² = 0.998) and the Langmuir model (R² = 0.996 for linear with qm=123.91 mg g-1, and R² = 0.993 for nonlinear fitting) more effectively described the adsorption of copper onto the adsorbent. In the fixed-bed column studies, among the well-known analytical models, the Log-Gompertz model showed better compatibility (R2 = 0.97∼0.99) between breakthrough curves with experimental results for various copper inlet concentrations. Also, numerical results obtained using computational fluid dynamics and mass transfer simulations with the linear driving force model were successfully validated by experimental results, particularly in the initial and transition zones of the breakthrough curve.

Isotherm, kinetic, and thermodynamic studies of adsorption of copper (II) and nickel (II) ions using low‐cost treated orange peel from aqueous solutions

AbstractThe aim of this study was to utilize processed orange peel waste (TOP) as an adsorbent to remove Cu(II) and Ni(II) ions from aqueous solutions. As a result of systematic experiments to determine the optimal conditions, it was determined that the most suitable conditions for the effective removal of Cu(II) ions were 400 mg/L initial concentration, 100 min contact time, 0.2 g adsorbent dosage, and a solution pH of 5.92. Similarly, the optimal conditions for the removal of Ni(II) ions were determined by systematic experiments to be 300 mg/L initial concentration, 0.2 g adsorbent dosage, 100 min contact time, and a solution pH of 6.19. The systematic experiments also included further investigation of the surface properties of TOP, and promising results were obtained by tests at three different temperatures (298, 308, and 318 K). The adsorption capacities for Cu(II), Ni(II), and Ni(II) were determined as 72.99, 75.18, and 76.33 mg/g, 42.55, 44.44, and 46.29 mg/g, respectively. Further analysis of the adsorption kinetics revealed that the pseudo‐second‐order model accurately represented the experimental data for both ions. Thermodynamic investigations provided strong evidence that the adsorption process of these noble metal ions on TOP is endothermic and spontaneous. The results of this study emphasize that TOP, with its low cost, easy‐to‐use nature, and high adsorption capacity, can be considered a long‐term solution for environmental remediation and water treatment in sustainable engineering applications.

The Development and Evaluation of Biosorbent Composite Spheres for the Adsorption and Quantification of Copper

Separation techniques are employed to treat and preconcentrate samples. Preconcentration commonly employs adsorption due to the wide range of sorbents available. The biosorbent composite has emerged as a highly effective alternative, primarily due to its selectivity for active sites and its impressive adsorption capability. This study aimed to assess and create a spherical biosorbent composite using cellulose acetate and avocado seed. The purpose of this work was to use a biosorbent composite for copper adsorption by flame atomic absorption spectrometry. The copper adsorption follows the Langmuir isotherm, which indicates that it occurs in a monolayer and is homogeneous. Additionally, the adsorption nature is favorable according to the RL factor. The highest capacity for copper adsorption is 0.121 mg g−1. The report describes the methodology and validation process for quantifying copper. The findings demonstrate that the composite biosorbent enables accurate preconcentration and quantification of copper found in decongestants.

Enhanced adsorption and recovery of copper and iron ions from wastewater using waste cellulose-loaded Mg(OH)2 composite

Enhanced adsorption and recovery of copper and iron ions from wastewater using waste cellulose-loaded Mg(OH)2 composite

Improving the wettability and lubrication properties of gallium-based liquid metal through the reaction adsorption of copper and gallium

Gallium-based liquid metal (GLM) is a promising lubricant used in extreme working conditions. In this paper, a copper-containing friction pair (316L-10Cu) is prepared, and the wettability and lubrication properties of GLM are improved by the reaction adsorption of copper and gallium. Compared with 316 L, the contact angle of GLM on 316L-10Cu surface decreases from 153° to 124°. At sliding speeds of 0.01 m/s (boundary lubrication) and 0.05 m/s (mixed lubrication), the friction coefficients of Si3N4/316L-10Cu decreases by 48.5 % and 24.6 % compared to Si3N4/316 L, and the wear rates decreases by 86.5 % and 80.7 %. The improved lubrication performance is attributed to copper doping promoting the adsorption of gallium on the frictional interfaces, and better wetting enhancing the hydrodynamic pressure effect of GLM.

Fundamentals of copper(II) adsorption on phyllosilicate minerals relevant to crud formation in solvent extraction from heap leach liquors

Because of the common presence of different silicate minerals, like kaolinite, montmorillonite and muscovite as gangue minerals in the beneficiation of copper oxide ores, the interaction between copper(II) ions in solution and each of these minerals is a field of strong interest, considering their implications on the aggregation of these minerals in the extreme pH conditions typical of hydrometallurgical unit operations for copper production. After copper adsorption isotherms determination at pH 2 and 4, specific adsorption data were fitted to both Langmuir and Freundlich models. It was found that adsorption is systematically larger at pH 4, and that montmorillonite is the mineral that displays a larger adsorption capacity, as in principle expected by its larger cation exchange capacity, CEC. A good fitting to the Langmuir model was obtained for the three samples, and montmorillonite also appears to conform to Freundlich isotherm predictions, as the tested concentrations of copper(II) do not allow to reach saturation. Furthermore, some desorption is measured for kaolinite and muscovite at the highest copper concentrations, probably because of significant interactions between the adsorbed ions. No such desorption was detected in montmorillonite samples. An XPS analysis of the surfaces of the three minerals suggests that copper adsorption in kaolinite is not associated to a cation exchange process but rather to electrostatic interactions between silica-like faces of the clay. In contrast, ionic exchange of structural calcium (for montmorillonite) or potassium (in the case of muscovite) seems to be the predominant mechanism of Cu(II) adsorption in the other two samples. Electrophoretic mobility determinations agree with this hypothesis: the mobility (always negative, with no traces of charge inversion) decreases in absolute value when kaolinite particles are in contact with solutions of increasing copper concentration at pH 2 or pH 4. On the other hand, the electrophoretic mobility values of muscovite and montmorillonite showed a weak pH and copper concentration dependence, a result that matches well with the ion exchange processes detected in the XPS measurements.

Recycling of water treatment plant sludge for copper adsorption from aqueous solutions

Recent studies have explored various adsorbent materials that are low-cost, available in quantity, and effective for heavy metal removal, one of them is the Water Treatment Plant (WTP) sludge. The study aimed to investigate the potential of recycling Water Treatment Plant sludge into an adsorbent for Cu (II) removal. The sludge adsorbent was carbonized by using a furnace at 600°C for 2 hours. This study was conducted in batch. The adsorbent effectiveness was analyzed by varying the dosage, contact time, and activation of the sludge adsorbent on Cu (II) removal. The adsorption isotherm was analyzed using the Langmuir and Ferundlich models, and the kinetic study used pseudo-first-order and pseudo-second-order model. The results showed the removal efficiency of Cu (II) for both activated and non-activated sludge adsorbents reached 98.6–99.9%. The addition of dosage did not affect the increase in Cu (II) adsorption capacity. Activation of the adsorbent increased the adsorption capacity of Cu (II) with the equilibrium time at 60–90 min, shorter than the non-activated adsorbent at 90–120 min. The adsorption isotherm model for both adsorbent types fitted well to the Langmuir model, indicating the adsorption process occurs in a single layer on a homogeneous surface. The adsorption kinetics followed pseudo-second-order with a high correlation coefficient. Water treatment sludge, an industrial by-product, has the potential to be an effective and low-cost adsorbent material for Cu removal.

Adding Value to Food Waste Hydrothermal Liquefaction: Use of the Aqueous Phase for Compost and the Char for Adsorption of Lead, Copper, and Nitrate

Adding Value to Food Waste Hydrothermal Liquefaction: Use of the Aqueous Phase for Compost and the Char for Adsorption of Lead, Copper, and Nitrate

TiO2-loaded phosphogypsum-modified biochar for the removal of ofloxacin and Cu2+: Performance, mechanisms, and toxicity assessment

The combined contamination of antibiotics and heavy metals usually occurs in aquaculture wastewater and has high ecological toxicity. Currently, most research only focuses on the removal of a single heavy metal or antibiotics, and there is little research on the simultaneous removal of both. Therefore, to effectively treat them, this study prepared TiO2-loaded phosphogypsum-modified biochar (TYBC450) for adsorption and photocatalytic removal of ofloxacin (OFL) and copper (Cu2+). The removal performance and mechanisms of OFL and Cu2+ were explored, and their ecological toxicity was assessed through zebrafish acute toxicity experiments. The results suggested a synergistic effect between OFL and Cu2+. The adsorption efficiencies of TYBC450 for OFL and Cu2+ were 88.16% and 90.87% (the adsorption capacities were 1.75 and 3.65 mg/g, respectively). Bridging, precipitation, and complexation effects were the main co-adsorption mechanisms. The photocatalytic efficiencies of OFL and Cu2+ were 91.23% and 72.09% (the rate constants were 0.0101 and 0.0045 min-1, respectively). OFL acted as a hole-trapping agent, while Cu2+ acted as an electron acceptor, hindering the combination of e- and h+. There were 12 intermediates in the OFL degradation process, which had lower toxicity than the mother organism. Both the cyclic regeneration and actual aquaculture wastewater application tests indicated that TYBC450 had potential application prospects.

Biochar modified by ammonium pyrrolidine dithiocarbamate for high selective adsorption of copper in wastewater

Biochar application in wastewater purification is extremely appealing. Although heteropolysaccharides like Gum Seyal biochar (BC GS500) display great surface area and porosity, the adsorption capacity for Cu (II) was relatively low due to the week-binding surface functional groups. In this work, an innovative modification with the chelating agent ammonium pyrrolidine dithiocarbamate (APDC) capable of selectively and effectively adsorbing Cu (II) was conducted. Gum Seyal biochar was grafted with pyrrolidine dithiocarbamate (C5H8NS2–), amine (–NH2), and imine (–NH) groups using APDC based on the “hard and soft acids and bases theory” (HSAB). Batch studies, along with characterization (FITR, XPS, and SEM-EDS), molecular electrostatic potential (MEP) mapping, and density functional theory (DFT) calculations, were implemented to investigate the adsorption performance and mechanism responsible for selectively adsorptive Cu (II) removal. It was found that Cu (II) adsorption by modified biochar occurred endothermically and spontaneously. The adsorption data at pH 5 matched the pseudo-second-order kinetic model and the Langmuir isotherm (211.24 mg/g). DFT calculations show that modified biochar selectively binds Cu (II) superior to common ions such as Mg (II) and Ca (II) through a unique chelating mechanism. Their performance in real electroplating wastewater was investigated, and the production cost was estimated. It was concluded that the modified biochar (BC APDC) could have high applicable potential for Cu (II)-laden wastewater purification.

The role of chitosan grafted copolymer/zeolite Schiff base nanofiber in adsorption of copper and zinc cations from aqueous media

The objective of this research was to develop and assess chitosan-grafted copolymer/HZSM5 zeolite Schiff base nanofibers for Cu2+ and Zn2+ adsorption from aqueous media. Nanofibers were prepared via electrospinning and characterized using XRD, FTIR, 1H NMR, FESEM, TGA, BET, and XPS. The study evaluated the effect of unmodified HZSM5 and Schiff base functionalization on adsorption capacities. Incorporating 10.0 wt% zeolite Schiff base as the optimum content into the chitosan-grafted copolymer significantly enhanced adsorption, achieving increases of 98.2 % for Zn2+ and 42.2 % for Cu2+. Specifically, Zn2+ adsorption increased from 27.6 to 54.7 mg/g, and Cu2+ from 67.1 to 95.4 mg/g. Factors such as temperature, pH, adsorption time, and initial cation concentration were analyzed. Kinetic studies revealed a double-exponential model, and isotherm analysis indicated a good fit with the Redlich-Peterson model, showing maximum monolayer capacities of 310.1 mg/g for Cu2+ and 97.8 mg/g for Zn2+ (pH 6.0, 240 min, 45 °C). The adsorption thermodynamics indicated a spontaneous and endothermic adsorption. Reusability tests showed minimal capacity loss (4.91 % for Cu2+ and 5.59 % for Zn2+) after five cycles. The nanofiber displayed greater selectivity for Cu2+ over Zn2+ in multi-ion systems and real electroplating wastewater, highlighting its potential for targeted heavy metal removal.

Sodium alginate/banana peels/reduced graphene oxide nanocomposite beads for effective removal of copper and nickel from aqueous solutions

The use of naturally derived nanocomposite beads to remove nickel and copper is gaining more attention due to its relative abundance, low toxicity, and strong affinity toward heavy metals. Most previous studies focus on removing single heavy metals using developed nanocomposite beads. This work prepared sodium alginate/banana peels/reduced graphene oxide nanocomposite beads through simple precipitation using banana peels, reduced graphene oxide, and sodium alginate. The formed nanocomposite beads were characterized and evaluated for the adsorption of nickel and copper from the aqueous phase at neutral pH. The Langmuir isotherm suggests the homogenous adsorption of metals on the surface of the bead. The maximum removal capacity is 85.32 mg/g and 95.79 mg/g for nickel and copper, respectively. This study provides new insight into utilizing banana peels, reduced graphene oxide, and sodium alginate for toxic metal remediation to overcome pollution problems.