Removal Of Pb Research Articles

Optimization of trypan blue and brilliant green dyes photocatalytic degradation and adsorption of lead(II) and chromium (VI) heavy metal ions by copper sulfide nanoparticles

The use of nanoparticles for to remove organic pollutants and heavy metals is a rapidly expanding field in environmental sciences. However, process optimization for practical, real-world applications is still underexplored. In this work, copper sulfide nanoparticles prepared from a single-source precursor were characterized using SEM, TEM, EDX, FTIR, and UV-visible spectroscopy. The copper sulfide nanoparticles demonstrated high photocatalytic degradation efficiency of trypan blue (TB) and brilliant green (BG) dyes. The as-prepared nanoparticles efficiently removed lead(II) (Pb2+) and chromium(VI) (Cr6+) ions. Response surface methodology (RSM) with a Box-Behnken design (BBD) was employed to optimize reaction time, pH, and nanoparticle dosage. The optimal conditions for TB degradation were pH 10.91, 77.46 minutes, and 4.999 g/L, while for BG, they were pH 3, 70 minutes, and 5 g/L. For Pb2+ removal, optimal conditions were pH 7.06, 100.38 minutes, and 0.94 g/L, and for Cr6+ removal, pH 3.03, 168.20 minutes, and 0.98 g/L. Under these optimal conditions, CuS nanoparticles achieved up to 99.35% degradation for TB, 100% for BG, 100% removal for Pb2+, and 98.54% for Cr6+. ANOVA confirmed the models' significance, with high regression coefficients (R²: 0.9852 for BG, 0.9846 for TB, 0.9980 for Pb2+, and 0.9901 for Cr6+). The CuS photocatalyst remained stable over three reuse cycles, with minimal efficiency reduction (8.88% for TB and 19.01% for BG). This study demonstrates the effectiveness of copper sulfide nanoparticles in environmental remediation and highlights the practicality of using RSM to optimize nanoparticles as efficient materials to remove organic dyes and heavy metal-laden wastewater.

Kenaf Biochar as an Eco‐Friendly Adsorbent for Removal of Cu(II) and Pb(II): Optimal Temperature, Adsorption Models, and Efficiency Evaluation

ABSTRACTThis study examined the adsorption capacities of biochars derived from kenaf (KF‐BCs) for the removal of heavy metals such as Cu(II) and Pb(II). The thermal decomposition temperature (300–750°C) significantly influenced the morphology and composition of KF‐BCs, enhancing their surface area, pore structure, and alkalinity. Among them, kenaf pyrolyzed at 750°C (KF‐750) was the most effective in removing Cu(II) and Pb(II), as validated by kinetic, equilibrium, and isotherm model analyses. Adsorption kinetics revealed that equilibrium was attained after 24 h, with chemisorption governing the process rate. Equilibrium adsorption conformed to the Langmuir and Freundlich models for Cu(II) and Pb(II), respectively. KF‐750 exhibited midrange adsorption capacities for Cu(II) and Pb(II) (23.47 ± 0.3 mg/g and 50.07 ± 0.9 mg/g, respectively), compared with the literature. The thermodynamic assessment revealed an endothermic process with positive ∆H0, indicating that higher temperatures favor metal adsorption. At low pH, adsorption decreased due to electrostatic repulsion, particularly affecting Cu(II). More than 99.8% of Cu(II) and Pb(II) were removed with a 5.00 g/L KF‐750 dose. The cation effect order on KF‐750 was Ca2+ > Mg2+ > Na+ > K+. Overall, KF‐750 demonstrates promising potential as an adsorbent for the efficient heavy metal removal from aqueous solutions, presenting a viable option for environmental remediation.

N-doped nano-casted carbon monolith for Pb (II) removal and photocatalytic degradation of thiamethoxam from aqueous solution.

Single rock-like N-doped carbon monolith (ND-PFCM) was successfully constructed via nanocasting method. Phenol formaldehyde resin was taken as carbon source and nitrogen was incorporated in monoliths through NaNH2 activation. The synthesized monoliths were used for the removal of Pb (II) from aqueous solution. Various characterization techniques, namely Brunauer-Emmett-Teller (BET), Raman spectroscopy, UV-visible diffuse reflectance spectra (DRS) UV-DRS, zeta potential, scanning electron microscopy (SEM), TEM (transmission electron microscopy), TGA (thermogravimetric analysis), and XPS (X-ray photoelectron spectroscopy), were utilized to characterize synthesized monolithic samples. The different parameters such as pH, adsorbent dosage, and time were enquired on the removal efficiency of monoliths toward Pb(II). ND-PFCM exhibited the highest adsorption capacity of 330.03mgg-1 in 180min at pH 6. This is attributed to the fact that the better texture properties and presence of nitrogen functional groups enhance the uptake of Pb (II) ions on the monolith surface. In the kinetic studies, pseudo-second-order model fitted best with the experimental data. Furthermore, the removal of thiamethoxam (TM) from aqueous solution was done by using different weight ratios of ND-PFCM under the visible light. The maximum removal efficiency of 97.35% with rate constant of 0.02085min-1was obtained in 160min. Moreover, monoliths exhibited good reusability for five consecutive cycles. The findings suggest that the synthesized monoliths exhibit characteristics suitable and eco-friendly for sustainable use in water treatment applications.

Photosystem modulation and extracellular silicification in green microalgae: Key strategies for lead tolerance and removal

The escalating contamination caused by lead ions (Pb2⁺) and its harmful effects on all life forms has raised global concerns. Certain microalgae thrive in metal mining sites characterized by low pH and high concentrations of Pb2⁺, which are usually prohibitive for many microorganisms. Little is known about the mechanisms underlying the adaptation of such microalgae to these hostile conditions. In this study, we elucidated the adaptive strategies of the green microalga Micractinium belenophorum strain AUMW, isolated from a lead mining site, and its application for the removal of Pb+2. Results revealed that strain AUMW can efficiently tolerate up to 200 ppm of Pb+2 in an F/2 medium. Further experimental variables were optimized through response surface methodology (RSM), and 99.6 % removal of Pb2⁺ was achieved. Novel adaptive responses of strain AUMW to high levels of Pb2⁺ include: (i) activation of metal-protective response by modulation of quantum yield (Fv/Fm) and non-photochemical quenching (NPQ) of photosystem II; (ii) extracellular silicification encapsulated cells of strain AUMW and altered cell morphology from oval to hexagonal; (iii) silicification prevented intracellular translocation of Pb+2; (iv) silicification boosted adsorption of Pb+2, thus enhanced its removal. This study offers new insights into the protective role of silicification in green microalgae and its potential for the removal of metals from metal-polluted sites, waste from energy storage battery industries, and spent batteries. It also provides a solid base to explore the genetic and metabolic pathways involved in the adaptation of strain AUMW to elevated levels of Pb+2.

Removal of Pb (II) ions using chitosan oligosaccharide/carboxymethyl starch blend crosslinked with glutaraldehyde: a study on batch adsorption

Removal of Pb (II) ions using chitosan oligosaccharide/carboxymethyl starch blend crosslinked with glutaraldehyde: a study on batch adsorption

Polymer-assisted synthesis of ternary magnetic graphene oxide nanocomposite for the adsorptive removal of Cr(VI) and Pb(II) ions

The presence of chromium [Cr(VI)] and lead [Pb(II)] ions in the water bodies have adverse effects on humans and aquatic life. Graphene oxide-based magnetic nanocomposites synthesized in the presence of chitosan (mGO/CS) or polyaniline (mGO/PA) as potential adsorbents for the removal of Cr(VI) and Pb(II) ions. The FTIR (Fourier transform infrared spectroscopy), EDX (Energy dispersive X-ray), XRD (X-ray diffraction) and SEM (Scanning electron microscopy) were employed to investigate the chemical composition, structural, elemental analysis, crystalline size and morphology of the nanocomposites. The FTIR results confirmed the synthesis of the nanocomposites by detecting peaks of specific functional groups. The average crystallite sizes of the mGO, mGO/CS, and mGO/PA nanocomposites were 17, 25, and 23 (nm), respectively, as determined by the Debye-Scherrer equation from the XRD data. Batch adsorption experiments were conducted for Pb(II) and Cr(VI) removal by varying the variables like pH, concentration of metal ions and contact time. The Box Behnken design (BBD) was used to optimize the adsorption parameters. Under the optimum conditions, mGO/CS and mGO/PA showed maximum removal percentages (%R) of 92.36 and 98.7 for Pb(II), and 85.25 and 93.08 for Cr(VI), respectively. The adsorption capacities were 110.84 and 118.44 mg/g for Pb(II), and 87.74 and 111.7 mg/g for Cr(VI) were obtained for mGO/CS and mGO/PA, respectively. The pseudo-second-order kinetic model and Langmuir isotherm fitted well to the experimental data and explain the adsorption mechanism of the nanocomposite materials for both metal ions.

Enhanced performance of amine and thiol chemically modified graphene oxide for effective removal of Hg(II), Pb(II), and Cr(VI) from aqueous solution

This study describes a novel adsorbent with a multidentate ligand that was facilely fabricated by covalently bonding 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole on graphene oxide (AHMT-PRGO). The AHMT-PRGO nano-adsorbent was used for the effective removal of Hg(II), Pb(II), and Cr(VI) from wastewater. The AHMT-PRGO nano-adsorbent was synthesized by a nucleophilic substitution reaction between GO acyl chloride and AHMT chelating ligand in the presence of tetrabutyl-ammonium bromide as a catalyst. The successful modifications were confirmed via several spectroscopic and electron microscopy instrumentations including UV–Vis, FTIR, Raman, XRD, XPS, SEM, and TEM. The maximum adsorption capacities of Hg(II), Cr(VI), and Pb(II) on the AHMT-PRGO nano-adsorbent were 370.0, 136.2, and 109.6 mg/g, respectively, exceeding those of most previously reported adsorbents. Additionally, the equilibrium contact times for Hg(II), Pb(II), and Cr(VI) were 60, 30, and 400 min, respectively. In a mixture of nine heavy metal ions containing 250 ppm of each ion, the AHMT-PRGO nano-adsorbent exhibited high selectivity for Hg(II) ions. Furthermore, the AHMT-PRGO nano-adsorbent showed high stability over five adsorption–desorption cycles. Additionally, the AHMT-PRGO nano-adsorbent was successfully applied to remove heavy metal ions from real water samples. The novelty of AHMT-PRGO lies in the combination of a multidentate ligand for strong and selective binding with the high surface area and stability offered by covalently bonded graphene oxide. This combination offers potential advantages over traditional adsorbents in terms of adsorption capacity, selectivity, and reusability.

Efficient removal of lead from polluted paddy soil by one-pot synthesized Nano-Fe3O4 incorporated stable lignin hydrogel

Lead (Pb) contamination in agricultural soils poses a significant threat to both ecosystems and human health. While nano-Fe3O4 exhibits promising potential for Pb remediation, its practical application in the soil is hindered by its’ biotoxicity, easy aggregation, and the risk of secondary pollution. Thus, this study presents a novel approach wherein Fe3O4 was incorporated into hydrogel via a one-pot synthetic strategy (Fe3O4@LH). This incorporation enhanced the mechanical properties and environmental stability of the hydrogel composites. Based on the mechanical properties, environmental stability, and single-point adsorption results for Pb, we selected Fe3O4@LH-4 for further research. The removal mechanism and the feasibility of employing Fe3O4@LH-4 for Pb removal from paddy soil were investigated through batch adsorption experiments and soil culture studies. Results showed that the adsorption process was primarily governed by swelling adsorption, electrostatic adsorption, ion exchange, precipitation, nanometer effect, and complexation mechanisms. The application of Fe3O4@LH-4 significantly led to the reduction of 16.7 %–25.4 % in soil Pb content, with removal rates escalating alongside increased dosage and application periods of Fe3O4@LH-4. Fitting results of the prediction model indicated that the Pb content in mildly Pb-contaminated soil (186.55 mg/kg) would decrease to be below the risk control standard for soil contamination of agricultural land in China (140 mg/kg) after 112 days of continuous application. Concurrently, cadmium and arsenic contents in the soil decreased by 5.2 %–10.8 % and 7.1 %–16.7 %, respectively. Moreover, the application of Fe3O4@LH-4 positively influenced soil nutrient levels, with total nitrogen and soil organic matter content significant increments of 13.6 %–41.0 % and 4.6 %–16.1 %, respectively. Furthermore, Fe3O4@LH-4 recovery exceeded 88.3 % after a 90-day application period. These findings underscore the potential of Fe3O4 incorporated hydrogel as a promising agent for the sustained removal of heavy metal Pb from paddy soil.

Efficient removal of Pb(II) and Cd(II) ions from wastewater using amidoxime functionalized graphene oxide

AbstractThis study aimed to develop iminodiethylamine oxime graphite oxide (IOGO) through the grafting of iminodiethylamine oxime onto graphene oxide (GO) via amidation and oximation. The primary objective was to investigate the adsorption characteristics of Pb(II) and Cd(II) ions on IOGO. Results demonstrated that IOGO exhibited exceptional adsorption capabilities, reaching maximum adsorption capacities of 798.87 mg/g for Pb(II) and 283.50 mg/g for Cd(II). Remarkably, IOGO maintained its high adsorption performance over five consecutive adsorption cycles. Specifically, the adsorption capacity for Pb(II) remained significantly stable at 480.78 mg/g, exhibiting only an 8.77% decrease. Similarly, the Cd(II) adsorption capacity remained robust at 204.13 mg/g, demonstrating a modest reduction of 10.47%. These findings underscore the feasibility of employing IOGO in repeated adsorption processes, thereby showcasing its potential for practical applications in the removal of heavy metals from aqueous solutions.

Simultaneous Oxidation of Trace Organics and Sorption of Trace Metals by Ferrate (Fe(VI))-Coated Sand in Synthetic Wastewater Effluent.

The increased presence of toxic chemicals in aquatic matrices and their associated health effects raise the need for more effective treatment technologies. The application of Fe(VI), an advanced oxidation treatment agent with disinfecting and coagulating capabilities, is limited by Fe(VI) aqueous instability. Our previous study proposed an Fe(VI)-coated sand media to overcome this constraint and demonstrated that Fe(VI)-coated sand was an effective medium for the treatment of phenolic compounds. In this study, we assessed the potential of the media for treatment of acetaminophen (ACM), benzotriazole (BZT), sulfamethoxazole (SMX), copper (Cu), lead (Pb), and zinc (Zn)-common contaminants found in wastewater effluents-in ultrapure and synthetic wastewater effluent. Fe(VI)-coated sand reactivity was influenced by the solution pH and aqueous chemistry. For example, the removal of Pb improved by 39% in the presence of trace organics, indicating that trace metal removal was enhanced by Fe(III) phases formed during Fe(VI) reactions with trace organics. While oxidation of trace organic compounds increased as pH decreased, trace metal sorption was more favorable at higher pH (i.e., pH 8 and 9). The oxidation efficiency of trace organics by the media was the highest for ACM and SMX while BZT degradation was limited due to formation of Cu-BZT complexes. Batch tests in synthetic wastewater effluent revealed that the presence of divalent cations (i.e., Ca2+ and Mg2+) can catalyze Fe(VI) self-decay and promote Fe(III) production and subsequent trace metal removal; however, oxidation of trace organics was hindered in this matrix. This study highlights the potential for Fe(VI)-coated sand application for the treatment of complex matrices more representative of natural and engineered aquatic systems.

Effective Removal of Pb(II) from Multiple Cationic Heavy Metals—An Inexpensive Lignin-Modified Attapulgite

To develop cost-effective heavy metal adsorbents, we employed water-soluble lignin from black liquor to modify activated attapulgite, resulting in the creation of a novel adsorbent called Lignin-modified attapulgite (LATP). In this study, scanning electron microscopy and Fourier transform infrared spectrometer techniques were utilized to characterize the structural details of LATP. The results revealed that lignin occupies the micropores of attapulgite, while additional functional groups are present on the attapulgite surface. We conducted adsorption tests using LATP to remove five types of heavy metal ions (Cd2+, Pb2+, Zn2+, Mn2+, Cu2+), and it was found that LATP exhibited greater removal mass and binding strength for Pb(II) compared to the other ions. For further investigation, batch experiments were performed to evaluate the adsorptive kinetics, isotherms, and thermodynamics of Pb2+ removal from aqueous solutions using LATP. The results indicated that the adsorption capacity of Pb(II) on LATP decreased with decreasing pH, while the presence of Na+ had no effect on adsorption. The adsorption process reached equilibrium rapidly, and the Langmuir adsorption capacities increased with temperature, measuring 286.40 mg/g, 315.51 mg/g, and 349.70 mg/g at 298 K, 308 K, and 318 K, respectively. Thermodynamic analysis revealed positive values for ΔH0 and ΔS0, indicating an endothermic and spontaneous adsorption process. Furthermore, ΔG0 exhibited negative values, confirming the spontaneous nature of the adsorption. Consequently, LATP demonstrates great potential as an effective adsorbent for the removal of Pb(II). Therefore, LATP shows great potential as an effective adsorbent for the removal of Pb(II) from natural water environments, contributing to the sustainable development of man and nature.

Utilizing triethylenetetramine-functionalized MIP-206 for highly efficient removal of Pb(II) from wastewater

The global concern over heavy metal pollution necessitates urgent measures to safeguard human health and the environment. This study focuses on employing triethylenetetramine (TETA)-functionalized MIP-206-OH (TMIP-206) as an effective adsorbent for removing Pb(II) from wastewater. TMIP-206 was synthesized via a hydrothermal method followed by functionalization with TETA. Kinetic studies demonstrate that lead removal on TMIP-206 conforms to the pseudo-second-order model, indicating an efficient removal process. Experimental results reveal that TMIP-206 aligns with the Langmuir isotherm, exhibiting a maximum removal capacity of 267.15 mg/g for lead ions. The sorption efficiency of TMIP-206 for Pb ions remains stable across six cycles, with a reduction of less than 15%. Optimal adsorption performance is observed at a pH of 6. These findings underscore the potential of TMIP-206 as an alternative for adsorbing Pb(II) from aqueous environments, addressing the global challenge of heavy metal pollution. Future research should explore the scalability and long-term stability of TMIP-206-based adsorbents to enhance their practical applicability in diverse environmental contexts and contribute to broader strategies for mitigating heavy metal contamination.

Application of South African heulandite (HEU) zeolite for the adsorption and removal of Pb2+ and Cd2+ ions from aqueous water solution: Experimental and computational study

The capacity of South African Heulandite (HEU) zeolite to remove Pb2+ and Cd2+ ions from aqueous solution was investigated using batch experiments and molecular simulations studies. The effect of different factors on the adsorption of these ions onto the zeolite was investigated; contact time, initial metal ion concentration and the amount of HEU adsorbent. Molecular simulations was done using Monte Carlo and density functional theory. Experimental results obtained indicate that the maximum adsorption for the two ions occur at pH 5 and after 240 min of contact time. The percent removal based on contact time of Pb2+ and Cd2+ ions from water by the heulandite zeolite were 99.7 and 76.7 %, respectively. The adsorption of two metal ions onto the HEU zeolite follows the Langmuir adsorption isotherm. From the molecular simulation findings, the adsorption of Pb2+ ions onto the HEU window is equidistant from the two adjacent oxygen atoms within the HEU structure while the Cd2+ ion is adsorbed in the upper left side of the 8-ring HEU window. It was observed that the performance of the zeolite can significantly be improved by doping with germanium, aluminum, thallium indium, and sodium cations. These results indicate that the application of HEU zeolite as an adsorbent holds a great promise in heavy metal removal from aqueous solutions.

Utilizing Date Palm Leaf Biochar for Simultaneous Adsorption of Pb(II) and Iodine from Aqueous Solutions

This study addresses the environmental and health hazards posed by Pb(II) and iodine, two significant contaminants. The objective was to explore the adsorption of these substances from aqueous solutions using biochar derived from the leaf midribs of the date palm through a slow pyrolysis process. The pyrolysis was conducted in two stages within a vacuum furnace: initially at 300 °C for 1 h followed by overnight cooling, and then at 600 °C with a similar cooling process. The resulting biochar was characterized for its microstructural features and functional groups using scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy. It exhibited a porous structure with large numbers of pores (20 to 50 μm in size) and functional groups including O-H, C-H, and C=C, which are integral to its adsorption capabilities. For the adsorption studies, a 100 ppm Pb(II) ion solution was treated with varying amounts of biochar (20, 40, 60, and 80 mg) for 24 h. In parallel, iodine adsorption was tested, with biochar quantities ranging from 0.1 to 0.4 g/50 mL. Both treatments were followed by filtration and analysis using atomic absorption spectroscopy to determine the remaining concentrations of Pb(II) and iodine. The study also explored the effect of varying incubation periods (up to 30 h) on iodine adsorption. The results were significant; 100% adsorption of Pb(II) was achieved with the addition of 60 mg of biochar per 10 mL of solution. In contrast, for iodine, a maximum adsorption of 39.7% was observed with 30 mg or 40 mg of biochar per 50 mL. These findings demonstrate the potential of date palm-derived biochar as an effective and sustainable material for the removal of Pb(II) and iodine from contaminated water, offering valuable insights for environmental remediation strategies.

Role of arbuscular mycorrhizal fungi in lead translocation from Bidens pilosa L. plants to soil

Bidens pilosa frequently forms a symbiotic association with arbuscular mycorrhizal fungi (AMF). This plant species can grow in Pb-polluted soils, accumulating Pb in its tissues. The aims of the study were to determine whether Pb accumulated in the tissues of B. pilosa can be transferred to the soil through AMF and to compare the role of AMF communities that have a history of exposure to the contaminant with those that have never been exposed. The experiment combined plants with and without Pb accumulated in their tissues, and inoculated with AMF collected from the rhizosphere of B. pilosa in soils contaminated and not contaminated with Pb. The results showed that AMF participate in the removal of Pb that had entered the plant and release it into the soil, as evidenced by the presence of Pb in the AMF spores and in the glomalin produced by AMF. We propose that Pb accumulation in AMF spores would be a protection mechanism that interrupts Pb uptake by the plant; however, that mechanism would not be fully exploited in detoxification, whereas the production of Pb-enriched glomalin could be an important detoxification mechanism to eliminate Pb already taken up by plants. AMF with a history of Pb exposure achieved only higher rates of root colonization, while AMF without previous exposure showed higher Pb concentration in the spores and higher glomalin production, and successfully removed Pb from both the roots and aboveground parts of the plant. The use of AMF communities not adapted to Pb may be a more effective option for microbe-mediated phytoremediation methods in which detoxification mechanisms are desirable.

Characterization of phosphate modified red mud-based composite materials and study on heavy metal adsorption.

In this paper, Bayer red mud (RM) and lotus leaf powder (LL) were used as the main materials, and KH2PO4 was added to modify the material. Under the condition of high-temperature carbonization, RMLL was prepared and phosphate modified red mud matrix composite (PRMLL) was prepared based on KH2PO4 modification, which can effectively remove Pb2+ from water. The optimum preparation and application conditions were determined through orthogonal experiment: dosage 0.1g, ratio 1:1, and temperature 600 °C. The effects of pH, dosage, and initial concentration on the adsorption of Pb2+ were studied. The pseudo-first-order, pseudo-second-order, and Elovich kinetic models were fitted to the experimental data. It was found that RMLL and PRMLL were more consistent with the pseudo-second-order kinetic model and chemisorption. Langmuir, Freundlich, Timkin, and Dubinin-Radushkevich isothermal adsorption models were used to fit the experimental data. It was found that RMLL and PRMLL were more consistent with Langmuir model. In addition, the maximum adsorption capacity of RMLL and PRMLL was 188.1 mg/g and 213.4 mg/g, respectively. It is larger than the adsorption capacity of their monomers. Therefore, the use of RMLL and PRMLL as the removal of Pb2+ from water is a potential application material.

Valorization of castor seed shell waste as lead adsorbent by treatment with hot phosphoric acid: Optimization and evaluation of adsorption properties

Lead is used in many industries such as refining, mining, battery manufacturing, smelting. Releases of lead from these industries is one of the major public health concerns due to widespread persistence in the environment and its resulting poisoning character. In this work, the castor seed shell (CSS) waste was exploited for preparing a beneficial bio-adsorbent for removal of Pb(II) ions from water. The raw CSS was modified with H3PO4 at different acid concentrations, impregnation ratios, activation times, and temperatures. An optimum adsorption capacity was observed for CSS modified with 2 M acid, 5 mL g−1 solid to liquid ratio, treated at 95 °C for 160 min. Exploiting acid modification, the SEM, XRD, and FTIR analyses show some alterations in functional groups and the surface morphology of the biomass. The impacts of physiochemical variables (initial lead ions concentration, pH, adsorbent dose and adsorption time) on the lead removal percentage were investigated, using response surface methodology (RSM). Maximum removal of 72.26% for raw CSS and 97.62% for modified CSS were obtained at an initial lead concentration (50 mg L−1), pH (5.7), adsorption time (123 min) and adsorbent dosage (1.1 g/100 mL). Isothermal and kinetics models were fitted to adsorption equilibrium data and kinetics data for the modified CSS and the adsorption system was evaluated thermodynamically and from the energy point of view. Isothermal scrutinization indicated the mono-layer nature of adsorption, and the kinetics experimental outcomes best fitted with the pseudo-second-order, implying that the interaction of lead ions and hot acid-treated CSS was the rate-controlling phenomenon of process. Overall, results illustrated that the hot acid-treated biomass-based adsorbent can be considered as an alternative bio-adsorbent for removing lead from water media.

Selective capacitive removal of Pb(II) ions from industrial wastewater using NF/Mn2CoO4@MoO2 electrodes

To achieve targeted removal of Pb2+ from industrial wastewater, a NF/Mn2CoO4@MoO2 composite electrode, synthesised using the hydrothermal method combined with electrodeposition technology, was employed to construct an asymmetric capacitive deionization (CDI) system to selectively electro-adsorb and desorb Pb2+ ions. The electrode exhibited pseudocapacitive characteristics in solutions containing Pb2+, facilitating rapid and reversible redox reactions. The asymmetric CDI system, utilising graphite paper as the positive electrode and NF/Mn2CoO4@MoO2 as the negative electrode, displayed exceptional adsorption performance at 1.4 V for 1 h, decreasing the Pb2+ concentration from 50 ppm to 4 ppb, achieving an adsorption capacity of 156.24 mg g−1, and displaying outstanding cyclic stability. Moreover, the electrode demonstrated preferential adsorption of Pb2+ in mixed solutions containing multiple heavy metal ions, with relative removal coefficients of 4.48 − 19.86 compared with other ions. Analysis of the adsorption mechanism indicated that during the adsorption process, Pb2+ was embedded between MoO2 layers, disrupting the electron cloud symmetry and triggering an oxidation reaction. Octahedral MoO2 then lost electrons and transformed into tetrahedral [MoO4]2-, forming PbMoO4 with embedded Pb2+ between the layers, and achieving effective removal of Pb2+ with high selectivity. Molecular dynamics simulations and density functional theory (DFT) calculations confirmed the high selectivity of the prepared electrode for Pb2+ ions based on stronger binding of Pb2+ to MoO2 than other ions. The electrode has application potential for the capacitive removal of Pb2+ from industrial effluent through CDI technology.

Synthesis and fabrication of magnetically separable phosphate-modified magnetic chitosan composites for lead(II) selective removal from wastewater

To address the urgent need for efficient removal of lead-containing wastewater and reduce the risk of toxicity associated with heavy-metal wastewater contamination, materials with high removal rates and easy separation must be developed. Herein, a novel organic-inorganic hybrid material based on phosphorylated magnetic chitosan (MSCP) was synthesized and applied for the selective removal of lead (II) from wastewater. From the characterization and the experimental results can be obtained that the magnetic saturation strength of MSCP reaches 14.65 emu/g, which can be separated quickly and regenerated readily, and maintains high adsorption performance even after 5 cycles, indicating that the adsorbent possesses good magnetic separation performance and durability. Also, MSCP showed high selective adsorption performance for lead in the multiple metal ions coexistence solutions at pH 6.0 and room temperature, with an adsorption coefficient SPb-MSCP of 78.85%, which was much higher than that of MSC (the SPb-MSC was 11.59%). Additionally, in the single lead system, the sorption characteristics of Pb(II) on MSCP and MCP had obvious pH-responsiveness, and their adsorption capacity increased with the increase of solution pH, reaching the maximal values of 80.19 and 72.68 mg/g, respectively. It is noteworthy that the acid resistance of MSCP with an inert layer coated on the core is significantly improved, with almost no iron leaching from MSCP over the entire acidity range, while MCP has 7.63 mg/g of iron leaching at pH 1.0. Significantly, MSCP exhibited a maximum adsorption capacity of 102.04 mg/g, which matches the Langmuir model at pH 6.0 and 298.15 K, and points to the pseudo-second-order kinetics of the chemisorption process of Pb(II) on MSCP. These findings highlight the great potential of MSCP for Pb(II) removal from aqueous solution, making it a promising solution for Pb(II) contamination in wastewater.

Facile and economic preparation of graphene hydrothermal nanocomposite from sunflower waste: Kinetics, isotherms and thermodynamics for Cd(II) and Pb(II) removal from water

Keeping the need for good water quality and the demand of climatic issues, the sunflower waste was converted into graphene hydrothermal nanocomposite absorbents for the removal of toxic Cd(II) and Pb(II) metal ions from water. The graphene composite materials were studied by scanning (SEM) and transmission electron microscopy (TEM), XRD analysis, TG and DSC, Raman and IR spectroscopy. According to SEM and TEM analysis, the decarbonized materials had a disordered structure with amorphous carbon with a small pore content. During the carbonization process, the pores space was opened due to the removal of amorphous organic matter and the formation of defects; providing a significant number of meso- and micropores. The prepared graphene composite showed 133.33 and 222.22 mg/g Langmuir adsorption of Cd(II) and Pb(II) at pH 6.0, dose 0.33 g/30 mL, initial concentration 300 mg/L, time 30 min and at 45 °C temperature using hydrothermal nanocomposite HTC/graphene oxide absorbent. The obtained results followed the sorption of heavy metal ions in a mixed-diffusion mode with the contribution of a second-order reaction between the active center of the sorbent and the metal ions. The Temkin and Dubinin-Radushkevich model’s parameters and thermodynamic results confirmed endothermic physical interactions among adsorbent and metal ions. This paper is highly useful for managing sunflower waste and purifying water; leading to the present demand for clean water and climatic issues. The production of the effective low-cost nanocomposite using green synthesis technologies (hydrothermal carbonization of raw materials) is highly useful for the removal of Cd(II) and Pb(II) toxic metal ions from water.