Removal Of Copper Ions Research Articles

Copper Ion Removal by Adsorption Using Fly Ash-Based Geopolymers: Process Optimization Insights from Taguchi and ANOVA Statistical Methods.

The present study aimed to use geopolymer materials synthesized from different fly ashes, which are promising for the adsorption of copper ions from aqueous solutions. The characterization of fly ashes and prepared adsorbents was performed by energy-dispersive X-ray spectroscopy (EDS) analysis, Brunauer-Emmett-Teller (BET) surface area analysis, and Scanning Electron Microscopy (SEM). Taguchi and ANOVA methods were used to predict the effect of different working parameters on copper ion removal by prepared geopolymers. Based on data obtained by the Taguchi method, it was found that the factor most influencing the adsorption process is the type of adsorbent used, followed by the solution pH, the reaction time, the adsorbent dose, and the initial copper ion concentration. The ANOVA results agree with the Taguchi method. The optimal conditions of the adsorption process were: fly ash C modified by direct activation with 2 M NaOH, at 70 °C for 4 h, solution pH of 5, initial pollutant concentration of 300 mg/L, 40 g/L adsorbent dose, and 120 min of reaction time. Copper ion removal efficiency was determined experimentally under optimal conditions, achieving a value of 99.71%.

Efficacy of mesoporous TiO2–ZrO2@g-C3N4 produced using a simple ultrasonic approach for copper ion removal from wastewater

The present study describes ultrasonically produced ternary composite material composed of carbon nitride nanosheets, zirconium, and titanium oxides for elimination of copper ions. The formation of monoclinic ZrO2, anatase TiO2, and g-C3N4 phases with respective crystallite sizes 6, 11, 13 nm were verified by the X-ray diffraction technique. The dispersion of the metal oxides nanoparticles with the graphitic nanosheets, the elemental composition of Zr, Ti, O, C and N, and the characteristic functional groups were verified respectively by TEM, EDX, and FTIR analysis that confirmed the successful formation and composition of the nanocomposite TiO2–ZrO2@g-C3N4 (TZCN). The good porosity of the composite that show a surface area, pore volume, and pore diameter values of 47.42 m2/g, 0.056 cm3 g−1, and 20.3 Å that nominate it for adsorption application. The adsorption capabilities of the nanocomposite were studied for copper ion removal from an aqueous solution, as well as the impacts of pH and starting Cu2+ concentration. The results show that the adsorption process is pH and starting concentration-dependent, with a maximum adsorption capacity of 447.8 mg/g. The Cu2+ adsorption is a monolayer chemisorption process that is well described by the Langmuir adsorption model and follows pseudo-second-order kinetics. Moreover, a plausible mechanism for Cu2+ ion adsorption on the surface of TZCN nanocomposite particles is proposed.

Highly selective and sensitive colorimetric chemosensor using PVA/chitosan ion-imprinted nanofibers for copper ion detection and removal

Herein, a highly efficient colorimetric chemosensor incorporating ion-imprinted electrospun nanofiber was developed for the removal and detection of Cu2+ ions. In this regard, PVA/chitosan composites were used as the polymeric matrix, and 1-(2-pyridylazo)-2-naphthol was employed for complex formation. The prepared naked-eye sensor was characterized using Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, atomic force microscopy, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction analysis, revealing the morphological, structural, and molecular properties of the sensor.The results showed that the colorimetric chemosensor based on copper-imprinted nanofiber (Cu–INF) possesses higher selectivity for Cu2+ compared to interference ions. The selectivity coefficient (k) and relative selectivity coefficient (K′) indicated the selective behavior of Cu–INF in the adsorption of Cu2+ in binary systems including Cu2+/Co2+, Cu2+/Ni2+, and Cu2+/Zn2+.Furthermore, the ion-imprinted nanofiber was used for the preconcentration of copper ions, demonstrating a high adsorption capacity of 128.205 mg g−1 for Cu2+. The equilibrium adsorption isotherm and adsorption kinetics of Cu2+ on Cu–INF followed the Freundlich adsorption isotherm and a pseudo-second-order model, respectively. The developed sensor exhibited a linear detection range of 5 × 10−8 - 2 × 10−7 M with a limit of detection (LOD) of 1.07 × 10−8 M for copper ions. The results indicated satisfactory adsorption and successful detection of Cu2+ at trace concentrations.

Preparation of a fly ash-based porous geopolymer material for copper ion removal

Preparation of a fly ash-based porous geopolymer material for copper ion removal

Synthetic Zeolite from Blast Furnace Slag (BFS) as an effective sorbent for simultaneous removal of Cadmium and Copper ions

The main challenge for remediation of metals contaminated water is the application of a proper, effective, low-cost material for decontamination of hazardous metal. In this study, low-cost zeolite derived from blast furnace slag (Z-BFS) by a facile hydrothermal method was investigated for adsorption of copper (Cu2+) and cadmium (Cd2+) ions from aqueous solutions. Furthermore, the characteristics of the prepared Z-BFS were evaluated via different techniques (FT-IR, XRF, XRD, SEM and EDX). The results showed the complete removal of Cd2+ and Cu2+ ions. Notably, the maximum adsorption capacity of metals had the trend Cu2+ (103 mg/g) > Cd2+ (80 mg/g) within 20 min at pH 5.5 and 2 g Z-BFS/l. The experimental data fit well with the pseudo-second order kinetic model elucidating that chemisorption is the rate determining step. The isotherms of adsorption were satisfactorily described by the Langmuir isotherm model indicating the monolayer adsorption process. The thermodynamic study demonstrated that adsorption process is endothermic. The obtained results from this study show that Z-BFS proves to be a proper candidate adsorbent for the removal of Cd2+ and Cu2+ ions from contaminated water.

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.

Microporous hydrophilic super-oxidized carbons with high surface area for removal of copper ions

Super-oxidized porous carbons produced from reduced graphene oxide have been demonstrated recently to show unique sorption properties. Here we report experiments with identical oxidative treatment applied to four very different types of porous carbon materials with extremely broad range of specific surface area (SSA) ∼350–3400 m2 g−1. It is demonstrated that KOH-activated carbons can be oxidized to the same degree as graphene oxide (GO) while preserving a larger part of SSA. Prolonged oxidation with ammonium persulfate resulted in extraordinary high degree of oxidation with C/O ratio reaching 2.1. Precursor carbons with largest share of micropores are found to be more stable against oxidative treatment, while single-walled carbon nanotubes (SWCNT's) are oxidized to much less extent. While mesopores collapse, micropores survive strong oxidation treatment providing materials with rather narrow pore size distribution and high (for given oxidation degree) BET SSA up to ∼1150 m2 g−1. Super-oxidized porous carbons (SOPC's) show a high abundance of hydroxyl, epoxide, carbonyl, and carboxyl functional groups (similar to GO). As a result of oxidation, the hydrophobic carbons are converted into hydrophilic materials. Characterization shows that many properties of SOPC (e.g. degree of oxidation, type of functional groups, thermal stability etc.) are rather similar to GO, except for three-dimensional porous structure which can be considered an advantage for sorbent applications. SOPC's demonstrate superior sorption capacity for Cu(II) (up to ∼105 mg g−1), which is 8-fold higher than the value for non-oxidized precursor.

Monocomponent Biosorption of Copper Ions (II) onto Nanocrystalline Cellulose from Coconut Husk Fibers

Introduction: Nanocrystalline cellulose (NCC) is one of the most suitable cellulose derivatives for the treatment of wastewater. Various agricultural wastes have been used for the extraction of NCC. Coconut wastes have been widely studied as potential adsorbents for the removal of pollutants, including dyes and heavy metals. Methods: In this work, nanocrystalline cellulose (NCC) was successfully isolated from coconut husk fibers through alkaline pretreatment accompanied by sulfuric acid hydrolysis. Then, the ability of NCC to adsorb Cu2+ from aqueous solution in batch studies was investigated. Results: Results indicated that the optimal hydrolysis parameters were achieved at 50° C for 45 min with 64% sulfuric acid to extract NCC as rod-like particles with diameters between 4-10 nm. The potential of NCC as a biosorbent to remove copper ions (Cu2+) from aqueous solution was investigated in terms of batch mode and maximum adsorption capacity (qm) of 79.491 mg/g of Cu2+. The adsorption efficiency of Cu2+ions increased with an increase in the adsorbent dosage, decreased with an increase in the initial concentration of contaminant, and increased with the contact time. Under optimal conditions, adsorption kinetic followed a pseudo-second-order kinetic model and the adsorption isotherm fitted most closely with the Langmuir model. Conclusion: According to a literature review, NCC from coconut husk fibers has not been used for the adsorption of heavy metals, mainly copper ions. This study shows that NCC from coconut husk fibers can be used as a low-cost and environmentally friendly adsorbent for the removal of Cu2+ from aqueous solutions.

Removal of Copper and Zinc Metal Ions from Industrial Effluents in Continuous Mode using Modified Date Pits

Adsorbents based on agricultural biomass have been subjected to several investigations in recent years owing to their low cost and promising adsorption capabilities. This paper aimed to demonstrate the efficiency of utilizing date pits modified with hydrogen peroxide as agricultural biomass in extracting heavy metals from polluted water in a column continuous flow system. The resulting modified adsorbent (MDP) has a surface area of 278.18 m2/g. The derived adsorbent was investigated under changed operating parameters including the flow rate (4-12) ml/min, pH (4-10), initial metal ion concentration (30-60) mg/L, and temperature (20-50) °C to determine their effect on heavy metals adsorption efficiency. The response surface methodology (RSM) experimental design was utilized to study the primary and combined influence of four key parameters, including (A) initial metal ion concentration, (B) pH solution, (C) solution temperature, and (D) flow rates of the influent, on the metal removing efficiency (Re%). optimization in fact, an analysis of variance (ANOVA) revealed a high coefficient of regression, or R2 > 0.90. Furthermore, the removal efficiency was positively influenced by reducing the initial ion concentration, flow rate, and temperature. in addition, the pH shows maximum effectiveness at a neutral state. In general, Cu (II) adsorption shows a higher affinity to adsorb over the MDP surface compared to Zn (II). The MDP adsorbents exhibited a promising removal efficiency for metal ions and further investigations are needed.

Preparation of a New Heavy Metal Chelating Agent and Its Removal of Copper Ions in Wastewater

In this study, a new type of dithiocarbamate (DTCs) heavy metal chelating agent MF-DTC was prepared by carbon disulfide modified melamine formaldehyde resin prepolymer, and the structure of the chelating agent and chelating products was characterized by infrared, ultraviolet, elemental analysis, thermogravimetry, scanning electron microscopy and other means: the process of chelating agent Cu was studied, and the results showed that MF-DTC chelating agent had a higher adsorption capacity, and compared with the traditional chelating agent SDD and Na2S, it had higher chelating capacity under acidic conditions, it can be directly used to treat heavy metals in acidic wastewater. Moreover, the environmental stability of heavy metals after chelation is high. Heavy metals are not easy to be leached again after treatment.

MOF-derived Co-Al layered double hydroxide modified rice husk biochar nanohybrid for efficient removal of Cu (II) from wastewater

In this study, biochar-derived rice husk (RHB) was modified with Co-Al layered double hydroxide (LDH) derived from Co-based metal-organic framework (ZIF-67) through hydrothermal method to prepare RHB/ZIF-67-derived Co-Al LDH nanohybrid as adsorbent for efficient removal of copper (II) ions from aqueous medium. The nanohybrid was characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy (TEM), energy dispersive X-ray (EDX) spectroscopy, and N2 adorption-desorption. Atomic absorption spectroscopy (AAS) was employed to analyze the concentration of Cu (II) in aqueous solution. In order to investigate the effect of contact time, pH of solution, and adsorbent dose on the removal performance of RHB/ZIF-67-derived Co-Al LDH nanohybrid, batch experimental studies were conducted. The surface adsorption isotherm is well fitted to Langmuir model, and the adsorption mechanism follows the pseudo-second-order kinetic model. In addition, based on the central composite design in the response surface method, the optimal conditions for adsorbent dose, time, pH and initial concentration of Cu (II) are obtained as 2 mg, 3 min, 7 and 50 ppm respectively. In optimal conditions, the nanohybrid shows many advantages including the high removal percent (99.71 %) for Cu (II) ions, excellent adsorption capacity of 1377.94 mg g−1, the ability to reuse for five times, low cost, and compatibility with the environment. The combined properties of RHB and ZIF-67-derived Co-Al LDH provide a large surface area of 849.44 m2 g−1, which increases the contact surface of adsorbent with Cu (II) ions and endows great adsorption performance even in complex environments.

Synthesis of hydroxyapatite/activated carbon composite with bioactivity property and copper ion removal efficiency

Hydroxyapatite/activated carbon composite (HAP/AC) was synthesized via a one-pot method for an adsorption removal of copper ions (Cu2+) in water. The surface area, average pore size and pore volume of HAP/AC were found to be 296.41 m2 g−1, 3.5929 nm and 0.1509 cm3 g−1, respectively. The HAP/AC showed the Cu2+ removal efficiency of 99.68 % with the adsorption capacity of 299.05 mg g−1 at the initial concentration of 300 mg L−1, 50 °C and pH 5. The adsorption capacity of HAC/AC was higher than that of HAP and bare AC. The interaction between Cu2+ and HAP/AC adsorbent was suggested to be complexation, cation exchange, and electrostatic interaction. The adsorption followed the Freundlich isotherm model, indicating a non-uniform distribution of adsorption sites that led to multilayer adsorption with various binding energies. The adsorption kinetics fit well with the Pseudo-second order model with the amount of Cu2+ ions adsorbed at an equilibrium of 357.14 mgg−1. Thermodynamic studies indicated that the adsorption was spontaneous and endothermic with an increase in the randomness at the solid-liquid interface. In addition, the bioactivity test of HAC/AC showed that the growth of the newly-formed apatite increased with soaking time, demonstrating its potential in orthopedic implantology.

Removal and adsorption kinetics of copper(II) ions from aqueous media on activated carbon in dynamic adsorption on a fixed-bed column

Removal and adsorption kinetics of copper(II) ions from aqueous media on activated carbon in dynamic adsorption on a fixed-bed column

Design and characterization of phosphonic acid-functionalized grafted sepiolite nanohybrids and their adsorption studies for removal of copper ions from aqueous solution.

In this study, we synthesized novel, economically efficient phosphonic acid-functionalized grafted sepiolite nanohybrids for selective elimination of copper ions from water. These nanohybrids were prepared by graft polymerization of glycidyl methacrylate onto sepiolite. We utilized free radical graft polymerization to graft glycidyl methacrylate (GMA) onto silanized sepiolite. The nanohybrids obtained exhibited a grafting percentage of 479% at 0.3 g of KPS initiator, 15% GMA monomer, and after 4 h of reaction. In pursuit of selectively removing metal ions from water, the nanohybrid with the highest grafting (PGE3) was chemically treated with phosphoric acid to introduce phosphonic acid groups on it. FTIR, XRD, SEM, CHO analysis, BET, and TGA analysis were utilized to characterize the developed nanohybrids. Batch adsorption studies were carried out using AAS process, examining the impact of pH, adsorbent weight, contact time, adsorbate concentration, and temperature on the adsorption process. Due to the selectivity of phosphonic acid groups towards copper ions, phosphonic acid-functionalized grafted sepiolite nanohybrid (PGE3-P) was used for copper ions removal from its aqueous solution. The maximum adsorption capacity of PGE3-P adsorbents was 134.5 mg/g for copper ions. The data from kinetic studies suggests that the adsorption process of copper ions followed a pseudosecond-order model. Furthermore, Langmuir isotherm proved to be a more fitting model in equilibrium isothermal investigations. The thermodynamic analysis of the data indicates that the adsorption of copper ions by PGE3-P is an endothermic and spontaneous process. The development of this phosphonic acid-functionalized grafted sepiolite nanohybrid adsorbent is a new contribution into the field of adsorption. The developed material can be utilized as selective adsorbent for elimination of other heavy metals from water.

Removal of Iron and Copper Ions and Phenol from Liquid Phase by Membrane Based on Carbonaceous Materials.

The present work reports an effective method for the removal of inorganic and organic pollutants using membranes based on different carbonaceous materials. The membranes were prepared based on cellulose acetate (18 wt. %), polyvinylpyrrolidone as a pore-generating agent (2 wt. %) and activated carbon (1 wt. %). Activated carbons were developed from residues after extraction of the mushroom Inonotus obliguus using microwave radiation. It has been demonstrated that the addition of activated carbon to the membranes resulted in alterations to their physical properties, including porosity, equilibrium water content and permeability. Furthermore, the chemical properties of the membranes were also affected, with changes observed in the content of the surface oxygen group. The addition of carbon material had a positive effect on the removal of copper ions from their aqueous solutions by the cellulose-carbon composites obtained. Moreover, the membranes proved to be more effective in the removal of copper ions than iron ones and phenol. The membranes were found to show higher effectiveness in copper removal from a solution of the initial concentration of 800 mg/L. The most efficient in copper ions removal was the membrane containing urea-enriched activated carbon.

Batch adsorption studies on copper removal from an aqueous solution using natural zeolite: Process optimization

Abstract The ability of natural zeolite to remove copper ions from an aqueous solution was examined. The research aims to optimize adsorption operational variables, which include the amount of zeolite, pH, contact time, and initial heavy metal concentration for copper removal using zeolite. The research was conducted in batch experiments. The ranges of operational conditions are as follows: 0.2 - 1.0 g of zeolite, pH 4 - 8, 2 - 60 minutes of contact time, and 5 - 50 mg/L of initial concentration of copper. The outcomes indicated that the percentage removal of copper using zeolite achieved the best performance at an optimized adsorbent dosage of 1.0 g, a pH of 6, a contact time of 20 minutes with 135 rpm, and an initial copper concentration of 5 mg/L. To sum up, zeolite is an efficient adsorbent that is capable of separating copper from water-based solutions.

Facile preparation of cellulose nanofiber/ZSM-5 zeolite/polyethyleneimine aerogel for selective adsorption of Cu2+ in wastewater

The development of a cost-effective and environmentally friendly adsorbent is essential for effectively removing heavy metals from wastewater. This study presents the preparation of a recyclable cellulose nanofiber (CNF)/ZSM-5 zeolite/polyethyleneimine (PEI) aerogel through chemical crosslinking and freeze-drying techniques. The synthesized aerogel was applied for the highly selective adsorption of Cu2+. The characterization of the as-prepared aerogel indicates that its three-dimensional network porous structure, along with the abundance of active sites, contributes to the effective adsorption of Cu2+. The adsorption capacity was found to be 134.23 mg/g. Furthermore, it was observed that Cu2+ adsorbed by the composite aerogel could be efficiently eluted using 0.2 M EDTA-2Na. The adsorption kinetics and isotherm studies revealed consistency with the pseudo-second-order model and Langmuir model, indicating that the adsorption process was primarily governed by monolayer chemisorption. Mechanism analysis further confirmed that surface complexation, ion exchange, and electrostatic interaction were the primary driving forces behind the excellent adsorption capabilities of the prepared aerogel. Remarkably, the structural integrity and selective adsorption of the composite aerogel remained largely unchanged even after undergoing five sorption-desorption cycles. These findings strongly suggest that the CNF/ZEM-5/PEI composite aerogel holds significant promise for achieving efficient and selective removal of copper ions in wastewater.

BIO-ADSORPTION OF HEAVY METAL ION FROM WATER USING ACTIVATED CARBON

The discharge of effluent polluted with heavy metals have become a growing concern for researchers around the world. This study evaluated the removal efficiency of commercial activated carbon and rice husk activated carbon as adsorbents for the removal of copper ion in water. A nominal size of 1 mm was obtained after sieving the Rice Husk, washed with distilled water, dried in an oven t at 80 ℃ for 12 hours, and pyrolyzed in a furnace at 550 ℃ for 30 minutes. The chars produced were later air-dried and then activated with lemon juice. The Rice Husk Activated Carbon (RHAC) and Commercial Activated Carbon (CAC) purchased from the market were both subjected to the following analyses: bulk density, X-ray Fluorescence (XRF), Brunauer–Emmett–Teller (BET), Scanning Electron Microscope (SEM) and Energy Dispersive X-ray (EDX) in order to characterise the adsorbents and to understand their suitability for the removal of copper ion in water. One of the properties of an adsorbent is large pores which is exhibited by the activated carbons as revealed by the SEM analysis. Likewise, the XRF and EDX analyses confirmed that the adsorbents had larger proportion of Silica (50.1 – 50.25%), Carbon (60.06 – 84.87 wt .%) and Oxygen (15.13 – 21.60 wt. %) which is a property of a good adsorbent. BET analysis showed that the surface areas of the rice husk activated carbon and the commercial activated carbon were 998.35 and 1208.25 m2/g, respectively. The bulk densities of the rice husk activated carbon and the commercial activated carbon were 0.3325 and 0.2812 g/cm3, respectively. The maximum removal efficiency using RHAC was observed at 60 ℃ and 120 minutes at 83.96 and 89.21 %, respectively while for CAC the maximum removal efficiency was observed at 60 ℃ at 84.61 % and 30 minutes at 83.3 %. Initial concentration of 20 mg/l was observed to have the highest removal efficiency for the two activated carbon specimens. The modelled effect of initial concentration, temperature and contact time on removal efficiency yielded R2 values of 1, 0.918; 1,1 and 1,1 respectively for the CAC and RHAC.

Utilization of organic-rich materials for the adsorption of copper ions from aqueous environments

This study investigated the suitability of moss peat and compost as adsorbents for removing copper ions from aqueous systems. Kinetic experiments were conducted at pH 4, 20 °C, and an initial copper ion concentration of 20 mM. Under these experimental conditions, moss peat and compost had a maximum adsorption capacity of 45.8 and 41.9 mg/g, respectively. The kinetic data was assessed using several models, and the data fitted well with the pseudo-second-order model for both adsorbents. Moreover, the analysis of the isotherm data showed that the Langmuir model could fit the data, suggesting that copper ions are chemically adsorbed onto moss peat and compost. The pH value of 4.5 was the most effective for the adsorption of copper ions onto moss peat and compost. At this pH value, the maximum adsorption capacities were 60.0 mg/g for moss peat and 56.9 mg/g for compost. The characterization of moss peat and compost before and after the interaction with copper ions indicated that surface precipitation was the dominant mechanism by which copper ions were removed from aqueous systems. Copper precipitation on the surface of moss peat was higher than that on the surface of compost, and it was found to be 7.7 wt% and 3.8 wt%, respectively. Overall, these findings highlight the potential of using moss peat and compost as effective adsorbents for copper ions in highly contaminated water, particularly industrial and mining effluent.

Salted Dried Bamboo Shoots-Derived Mesoporous Carbon Inherently Doped with SiC and Nitrogen for Capacitive Deionization.

Dried bamboo shoots (DBS) are a natural resource with inherent silica content, which can serve as sacrificial templates for the formation of mesoporous carbon but also promote the generation of silicon carbide (SiC). Building on this, we introduced mesoporous and graphitic carbon/SiC (SiC/BSC) as the CDI electrode for copper ion (Cu2+) removal. Mesoporous carbon electrodes facilitate faster ion transport, diffusion, and electron-transfer pathways. Furthermore, SiC accelerates electron transfer and promotes faradic redox reactions during the charge and discharge processes. Consequently, the synergistic effect of SiC/BSC mesoporous carbon material leads to a promising electrode for Cu2+ capacitive deionization. Leveraging these unique properties, the SiC/BSC electrode material exhibits an outstanding CDI performance of 381.5 mg/g at 1.8 V. This study offers a strategy for the preparation of efficient mesoporous carbon materials as CDI electrodes, specifically tailored for the deionization of Cu2+ ions.