Recycling of Waste Toner Powder as Adsorbent to Remove Aqueous Heavy Metals

The removal of Cd²⁺, Zn²⁺ and Ni²⁺ from metal solutions onto waste toner power (WTP) was investigated. The influence of parameters such as pH, contact time, initial metal concentration and adsorbent dosage was studied in batch adsorption experiments. Batch equilibrium experiments showed that the highest removal efficiency for Zn²⁺ and Cd²⁺ occurs at pH 7, while pH 5 is the most suitable for Ni²⁺ removal. The amount of metal removed (mg/g) improved when increasing the initial concentration, and sorption of heavy metals reached equilibrium in 24 h. Metals’ uptake increased with increasing adsorbent dosage. The adsorption isotherms of Zn²⁺, Cd²⁺ and Ni²⁺ onto WTP fit the Langmuir better than the Freundlich model with correlation coefficient R² values ranging from 0.998 to 0.968 and 0.989 to 0.881, respectively. The data showed that the maximum adsorption capacity of heavy metals, a_max, ranged from 2.42 to 1.61 mg/g, from 6.22 to 2.01 mg/g and from 3.49 to 2.56 mg/g for Ni²⁺, Zn²⁺ and Cd²⁺, respectively, with the three WTPs used in this study. This adsorbent can potentially be used to remove metal ions from wastewater.     

Adsorption of Heavy Metals Ions from Mining Metallurgical Tailings Leachate Using a Shell-Based Adsorbent: Characterization,Kinetics and Isotherm Studies

This study defines the optimal parameters that allow the use of waste mollusk shells (WS) to remove heavy metals from three mining and metallurgical leachates. First, the influence of parameters such as pH, contact time, initial metal concentration, adsorbent dose and the presence of co-ions in Cu²⁺, Cd²⁺, Zn²⁺ and Ni²⁺ adsorption was investigated in synthetic solutions. Metal uptake was found to be dependent on the initial pH of the solution, the removal rate increasing with the increase in pH, showing the highest affinity at pH 5–6. The removal efficiency at lower concentrations was greater than at higher values. The competitive adsorption results on bimetallic solutions showed that the adsorption capacity of the sorbent was restricted by the presence of other ions and suppressed the uptake of heavy metals compared to the single adsorption. Cu²⁺ was the metal that most inhibited the removal of Cd²⁺, Zn²⁺ and Ni²⁺. The Langmuir isotherm provided the best fit to the experimental data for Cu²⁺, Cd²⁺ and Zn²⁺ and the Freundlich isotherm, for Ni²⁺. The data showed that the maximum adsorption capacity a_max for Zn²⁺, Cd²⁺ and Cu²⁺, was 526.32 mg g⁻¹, 555.56 mg g⁻¹ and 769.23 mg g⁻¹, respectively. Sorption kinetics data best fit the pseudo-second-order kinetic model. The results obtained in the tests with three mining and metallurgical leachates showed that WS were effective in simultaneously removing several heavy metals ions such as Cu, Ni, Zn, Cd, Ni, As and Se.     

Carbon Derived from Jatropha Seed Hull as a Potential Green Adsorbent for Cadmium (II) Removal from Wastewater

Carbon from jatropha seed hull (JC) was prepared to study the adsorption of cadmium ions (Cd²⁺) from aqueous solutions under various experimental conditions. Batch equilibrium methods have been used to study the influences of the initial metal ion concentration (0.5–50 ppm), dosage (0.2–1 g), contact time (0–300 min), pH (2–7), and temperature (26–60 °C) on adsorption behavior. It has been found that the amount of cadmium adsorbed increases with the initial metal ion concentration, temperature, pH, contact time, and amount of adsorbent. A kinetic study proved that the mechanism of Cd²⁺ adsorption on JC followed a three steps process, confirmed by an intraparticle diffusion model: rapid adsorption of metal ions, a transition phase, and nearly flat plateau section. The experimental results also showed that the Cd²⁺ adsorption process followed pseudo-second-order kinetics. The Langmuir and Freundlich adsorption isotherm models were used to describe the experimental data, with the former exhibiting a better correlation coefficient than the latter (R² = 0.999). The monolayer adsorption capacity of JC has been compared with the capacities of the other reported agriculturally-based adsorbents. It has been clearly demonstrated that this agricultural waste generated by the biofuel industry can be considered a potential low-cost adsorbent for the removal of Cd²⁺ from industrial effluents.     

High Removal Efficiency of Diatomite-Based X Zeolite for Cu2+ and Zn2+

Diatomite-based X zeolite was obtained and its crystallinity, morphology, and interface properties were investigated by XRD, BET, SEM, EDS, and XRF. The obtained X zeolite possessed a unique meso-microporous structure and showed good ion exchange properties for Cu²⁺ and Zn²⁺. The pseudo-second-order model and Langmuir isotherm model can best describe the adsorption kinetics and isotherms of Cu²⁺ and Zn²⁺, respectively. The maximal adsorption capacities of X zeolite for Cu²⁺ and Zn²⁺ were 146 and 195 mg/g at 323 K, respectively. Meanwhile, the adsorption process for Cu²⁺ and Zn²⁺ were chemical adsorption and ion exchange, respectively. Furthermore, the adsorption data turned out to be an endothermic and spontaneous process. Compared with other reported materials, the adsorption capacity of X zeolite synthesized from diatomite was among the highest. Therefore, it could be a promising adsorbent for the disposal of wastewater that contains metal ions.     

Snail Based Carbonated-Hydroxyapatite Material as Adsorbents for Water Iron (II)

Carbonated hydroxyapatite (CHAp) adsorbent material was prepared from Achatina achatina snail shells and phosphate-containing solution using a wet chemical deposition method. The CHAp adsorbent material was investigated to adsorb aqua Fe(II) complex; [Fe(H₂O)₆]²⁺ from simulated iron contaminated water for potential iron remediation application. The CHAp was characterized before and after adsorption using infrared (IR) and Raman spectroscopy. The IR and the Raman data revealed that the carbonate functional groups of the CHAp adsorbent material through asymmetric orientation in water bonded strongly to the aqua Fe(II) complex adsorbate. The adsorption behaviour of the adsorbate onto the CHAp adsorbent correlated well to pseudo-second-order kinetics model, non-linear Langmuir and Freundlich model at room temperature of a concentration (20–100 mg L⁻¹) and contact time of 180 min. The Langmuir model estimated the maximum adsorption capacity to be 45.87 mg g⁻¹ whereas Freundlich model indicated an S-type isotherm curvature which supported the spectroscopy revelation.     

Synthesis and Characterization of Biopolymeric Chitosan Derived from Land Snail Shells and Its Potential for Pb2+ Removal from Aqueous Solution

Pb²⁺ is considered to be a very toxic pollutant in the aquatic environmental media. Biopolymeric chitosan synthesized from snail shell has been studied for its potential to remove heavy metals from aqueous solution. The experiments were conducted in the range of 1–50 mg/L initial Pb²⁺ concentration at 298 K. The effects of pH, adsorbent dosage and contact time on the adsorptive property of the adsorbent were investigated and optimized. The derived chitosan was characterized using Fourier transform infrared spectrometer (FT-IR) and X-ray florescence (XRF). The experimental data obtained were analysed using the Langmuir and Freundlich adsorption isotherm models. The Langmuir model and pseudo second order kinetic model suitably described the adsorption and kinetics of the process with regression coefficients of 0.99 and 1.00, respectively. Sodium hydroxide was a better desorbing agent than hydrochloric acid and de-ionized water. From the results obtained, it is concluded that synthesized biopolymers from land snail shells has the potential for the removal of Pb²⁺ from aqueous solutions.     

Fluoride Bio-Sorption Efficiency and Antimicrobial Potency of Macadamia Nut Shells

This paper presents the potential application of macadamia nut shells (MNS) in the bio-sorption of fluoride and its antimicrobial potency against common pathogens encountered in surface water resources. The efficiency of MNS in the sorption of fluoride was determined using batch mode experiments, while the antimicrobial potency was investigated using the well disc diffusion assay method. The maximum fluoride sorption capacity of 1.26 mg/g was recorded at an initial fluoride concentration of 5 mg/L, adsorbent dosage of 0.5 g/100 mL, contact time of 120 min and initial pH of 6. The adsorption kinetics data were better described with a pseudo second order model, indicating the dominance of the chemisorption mechanisms. The Langmuir adsorption isotherm model described the isotherm data suggesting a monolayered adsorption. The thermodynamic parameters, ∆Gº and ∆Hº, confirmed that F⁻ sorption by MNS is a spontaneous and endothermic process. The bio-sorbent was regenerated for seven continuous cycles when HCl was used as regenerating solution. The antimicrobial studies revealed that MNS has minimal activity towards Escherichia coli, Staphylococcus aureus and Klebsiella pneumoniae. The MNS showed potentials for application in bio-sorption of fluoride. However, the doping of MNS with metal ions is recommended to enhance its anti-microbial potency.     

Sorption of Heavy Metal Ions of Chromium,Manganese, Selenium,Nickel, Cobalt,Iron from Aqueous Acidic Solutions in Batch and Dynamic Conditions on Natural and Synthetic Aluminosilicate Sorbents

Zeolites are materials with known sorption properties. The sorption is thought to progress mainly by ion exchange with Na⁺, K⁺, Mg²⁺, Ca²⁺ or H⁺ from the zeolite exchange sites. The aim of the study was to compare the sorption properties of natural and synthetic zeolites on the example of the removal of selected metals from aqueous acidic solutions. Uptake experiments for selected ions of chromium, manganese, selenium, nickel, cobalt, and iron were performed using the batch and kinetic column methods. The sorption of the individual metal ions in mg per 1g of sorbent was determined for each sorbent. The relative affinity sequence of the examined cations toward the various sorbent was presented. The Langmuir model was used to model the adsorption equilibrium. Vermiculite under 1 mm of diameter (SF), Na-X, and Na-A were proved to be the most suitable for the individual uptake of studied metal ions. It was observed that the behavior of selenium ions differed from the remaining ones which was interpreted that selenium undergoes adsorption in the anionic form. The fixed-bed column studies were performed using Na-A, ensuring the sorption of selenium in the presence of iron(III) ions. The experiments were conducted using Na-X zeolite pre-loaded by Fe(III) as well as unmodified sorbent eluted by an equimolar mixture containing 100 ppm of Fe and Se. Obtained results prove that selenium sorption improves if other metal ions such as iron appear in the acidic solution. That efficient selenium sorption conditions can be applied to remove selenium which was recognized as toxic at higher levels.     

Adsorption of Azo-Dye Orange II from Aqueous Solutions Using a Metal-Organic Framework Material: Iron- Benzenetricarboxylate

A Metal-Organic Framework (MOF), iron-benzenetricarboxylate (Fe(BTC)), has been studied for the adsorptive removal of azo-dye Orange II from aqueous solutions, where the effect of various parameters was tested and isotherm and kinetic models were suggested. The adsorption capacities of Fe(BTC) were much higher than those of an activated carbon. The experimental data can be best described by the Langmuir isotherm model (R² > 0.997) and revealed the ability of Fe(BTC) to adsorb 435 mg of Orange II per gram of adsorbent at the optimal conditions. The kinetics of Orange II adsorption followed a pseudo-second-order kinetic model, indicating the coexistence of physisorption and chemisorption, with intra-particle diffusion being the rate controlling step. The thermodynamic study revealed that the adsorption of Orange II was feasible, spontaneous and exothermic process (−25.53 kJ·mol⁻¹). The high recovery of the dye showed that Fe(BTC) can be employed as an effective and reusable adsorbent for the removal of Orange II from aqueous solutions and showed the economic interest of this adsorbent material for environmental purposes.     

Self-Supported Reduced Graphene Oxide Membrane and Its Cu2+ Adsorption Capability

Graphene stratiform membrane materials have been recently applied to heavy metal removal in aqueous systems via adsorption due to their high mechanical strength, chemical stability, and other properties. We applied reduced graphene oxide (rGO) alone as an adsorbent to remove heavy metal ions from wastewater. Self-supported rGO membrane was prepared using a green reduction method with sodium hydrosulfite. We used the Raman spectra to observe the structure of the rGO membrane. The morphology of the self-supported membrane was measured by a scanning electron microscope. The Cu²⁺ adsorption performance was measured in terms of pH, reaction time, metal ion concentration, and temperature. The maximum Cu²⁺ adsorption capacity of the rGO membrane was found to be 149.25 mg/g. The adsorption process followed a pseudo-second-order kinetic model, and adsorption isotherms were simulated by the Freundlich model.     

Kinetics and Adsorption Isotherms of Amine-Functionalized Magnesium Ferrite Produced Using Sol-Gel Method for Treatment of Heavy Metals in Wastewater

This study is focused on the kinetics and adsorption isotherms of amine-functionalized magnesium ferrite (MgFe₂O₄) for treating the heavy metals in wastewater. A sol-gel route was adopted to produce MgFe₂O₄ nanoparticles. The surfaces of the MgFe₂O₄ nanoparticles were functionalized using primary amine (ethanolamine). The surface morphology, phase formation, and functionality of the MgFe₂O₄ nano-adsorbents were studied using the SEM, UV-visible, FTIR, and TGA techniques. The characterized nanoparticles were tested on their ability to adsorb the Pb²⁺, Cu²⁺, and Zn²⁺ ions from the wastewater. The kinetic parameters and adsorption isotherms for the adsorption of the metal ions by the amine-functionalized MgFe₂O₄ were obtained using the pseudo-first-order, pseudo-second-order, Langmuir, and Freundlich models. The pseudo-second order and Langmuir models best described the adsorption kinetics and isotherms, implying strong chemisorption via the formation of coordinative bonds between the amine groups and metal ions. The Langmuir equation revealed the highest adsorption capacity of 0.7 mmol/g for the amine-functionalized MgFe₂O₄ nano-adsorbents. The adsorption capacity of the nanoadsorbent also changed with the calcination temperature. The MgFe₂O₄ sample, calcined at 500 °C, removed the most of the Pb²⁺ (73%), Cu²⁺ (59%), and Zn²⁺ (62%) ions from the water.     

Effect of Aluminium Powder on Kaolin-Based Geopolymer Characteristic and Removal of Cu2+

This current work focuses on the synthesis of geopolymer-based adsorbent which uses kaolin as a source material, mixed with alkali solution consisting of 10 M NaOH and Na₂SiO₃ as well as aluminium powder as a foaming agent. The experimental range for the aluminium powder was between 0.6, 0.8, 1.0 and 1.2wt%. The structure, properties and characterization of the geopolymer were examined using X-Ray Diffraction (XRD), Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). Adsorption capacity and porosity were analysed based on various percentages of aluminium powder added. The results indicate that the use of aluminium powder exhibited a better pore size distribution and higher porosity, suggesting a better heavy metal removal. The maximum adsorption capacity of Cu²⁺ approached approximately 98%. The findings indicate that 0.8% aluminium powder was the optimal aluminium powder content for geopolymer adsorbent. The removal efficiency was affected by pH, adsorbent dosage and contact time. The optimum removal capacity of Cu²⁺ was obtained at pH 6 with 1.5 g geopolymer adsorbent and 4 h contact time. Therefore, it can be concluded that the increase in porosity increases the adsorption of Cu²⁺.     

Preparation of a Novel Millet Straw Biochar-Bentonite Composite and Its Adsorption Property of Hg2+ in Aqueous Solution

The remediation of mercury (Hg) contaminated soil and water requires the continuous development of efficient pollutant removal technologies. To solve this problem, a biochar–bentonite composite (CB) was prepared from local millet straw and bentonite using the solution intercalation-composite heating method, and its physical and chemical properties and micromorphology were then studied. The prepared CB and MB (modified biochar) had a maximum adsorption capacity for Hg²⁺ of 11.722 and 9.152 mg·g⁻¹, respectively, far exceeding the corresponding adsorption value of biochar and bentonite (6.541 and 2.013 mg·g⁻¹, respectively).The adsorption of Hg²⁺ on the CB was characterized using a kinetic model and an isothermal adsorption line, which revealed that the pseudo-second-order kinetic model and Langmuir isothermal model well represented the adsorption of Hg²⁺ on the CB, indicating that the adsorption was mainly chemical adsorption of the monolayer. Thermodynamic experiments confirmed that the adsorption process of Hg²⁺ by the CB was spontaneous and endothermic. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and a thermogravimetric analysis (TGA) showed that after Hg²⁺ was adsorbed by CB, functional groups, such as the –OH group (or C=O, COO–, C=C) on the CB, induced complexation between Hg and –O–, and part of Hg (ii) was reduced Hg (i), resulting in the formation of single or double tooth complexes of Hg–O– (or Hg–O–Hg). Therefore, the prepared composite (CB) showed potential application as an excellent adsorbent for removing heavy metal Hg²⁺ from polluted water compared with using any one material alone.     

Green Synthesis of Zinc Oxide Nanoparticles Using Red Seaweed for the Elimination of Organic Toxic Dye from an Aqueous Solution

This study aims to produce green zinc oxide nanoparticles (ZnO-NPs) derived from red seaweed (Pterocladia Capillacea) and evaluate their potential to absorb Ismate violet 2R (IV2R) ions from an aqueous solution. UV-vis spectrophotometry, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and a Brunauer–Emmett–Teller surface area analysis (BET) were used to analyze the structural, morphological, and optical features of the synthesized nanoparticles. The change in color of the chemical solution revealed the formation of zinc oxide nanoparticles. The FTIR examination confirmed the synthesis of both Zn and ZnO nanoparticle powder, with a BET surface area of 113.751 m² g⁻¹ and an average pore size of 2.527 nm for the synthesized adsorbent. Furthermore, the maximum removal effectiveness of IV2R was 99% when 0.08 g ZnO-NPs was applied at a pH of 6, a temperature of 55 °C, and a contact time of 120 min. The dye adsorption capacity of the ZnO-NPs was 72.24 mg g⁻¹. The adsorption process was also controlled by the Freundlich adsorption model and pseudo-second-order reaction kinetics. The adsorption of IV2R ions onto the ZnO-NPs could be represented as a nonideal and reversible sorption process of a nonuniform surface, according to Freundlich adsorption isotherms. In addition, the constant values of the model parameters were determined using various nonlinear regression error functions. Moreover, thermodynamic parameters such as entropy change, enthalpy change, and free energy change were investigated; the adsorption process was spontaneous and endothermic. The high capacity of the ZnO-NPs synthesized by red seaweed promotes them as promising substances for applications in water treatment for the removal of IV2R dye from aqueous systems.     

Graphene Oxide@Heavy Metal Ions (GO@M) Complex Simulated Waste as an Efficient Adsorbent for Removal of Cationic Methylene Blue Dye from Contaminated Water

Graphene oxide (GO) was heavily used in the adsorption process of various heavy metal ions (such as copper (Cu) and iron (Fe) ions), resulting in a huge waste quantity of graphene oxide@metal ions complex. In this research, the authors try to solve this issue. Herein, the GO surface was loaded with divalent (Cu²⁺) and trivalent (Fe³⁺) heavy metal ions as a simulated waste of the heavy metal in various removal processes to form GO@Cu and (GO@Fe) composites, respectively. After that, the previous nanocomposites were used to remove cationic methylene blue (MB) dye. The prepared composites were characterized with a scanning electron microscope (SEM), transition electron microscope (TEM), Fourier transmission infrared (FTIR), Raman, and energy-dispersive X-ray (EDS) before and after the adsorption process. Various adsorption factors of the two composites towards MB-dye were investigated. Based on the adsorption isotherm information, the adsorption process of MB-dye is highly fitted with the Langmuir model with maximum capacities (mg g⁻¹) (384.62, GO@Cu) and (217.39, GO@Fe). According to the thermodynamic analysis, the adsorption reaction of MB-species over the GO@Cu is exothermic and, in the case of GO@Fe, is endothermic. Moreover, the two composites presented excellent selectivity of adsorption of the MB-dye from the MB/MO mixture     

Preparation of Amidoxime Polyacrylonitrile Chelating Nanofibers and Their Application for Adsorption of Metal Ions

Polyacrylonitrile (PAN) nanofibers were prepared by electrospinning and they were modified with hydroxylamine to synthesize amidoxime polyacrylonitrile (AOPAN) chelating nanofibers, which were applied to adsorb copper and iron ions. The conversion of the nitrile group in PAN was calculated by the gravimetric method. The structure and surface morphology of the AOPAN nanofiber were characterized by a Fourier transform infrared spectrometer (FT-IR) and a scanning electron microscope (SEM), respectively. The adsorption abilities of Cu²⁺ and Fe³⁺ ions onto the AOPAN nanofiber mats were evaluated. FT-IR spectra showed nitrile groups in the PAN were partly converted into amidoxime groups. SEM examination demonstrated that there were no serious cracks or sign of degradation on the surface of the PAN nanofibers after chemical modification. The adsorption capacities of both copper and iron ions onto the AOPAN nanofiber mats were higher than those into the raw PAN nanofiber mats. The adsorption data of Cu²⁺ and Fe³⁺ ions fitted particularly well with the Langmuir isotherm. The maximal adsorption capacities of Cu²⁺ and Fe³⁺ ions were 215.18 and 221.37 mg/g, respectively.     

Efficient Removal of Nonylphenol Contamination from Water Using Optimized Magnesium Silicate

Nonylphenol (NP) is considered to be an environmentally toxic, endocrine-disrupting chemical that affects humans and ecosystems. Adsorption is one of the most promising approaches for the removal of nonylphenol contamination from water. Herein, in order to design an adsorbent with high adsorption capacity, magnesium silicate with different Mg/Si ratios was successfully synthesized by a sol–gel method at 60 °C. Magnesium silicate with a Mg/Si ratio of 1:6 was found to possess the best adsorption performance, with maximum 4−NP sorption 30.84 mg/g under 25 °C and 0.2 g/L adsorbent dose. The adsorption was negatively affected by increasing adsorbent dose and temperature. The kinetics and isotherm of 4−NP adsorption by Mg/Si were well described by the pseudo−second−order and Sips model, respectively, and behavior was proven to be physisorption−enhanced by a chemical effect. Detailed characterization by XRD, BET, and SEM confirmed that the magnesium silicate possesses an amorphous, mesoporous structure. The study will contribute to the applicability of cheap magnesium silicate for removal of NP contamination in water.     

Removal of Fe2+ and Mn2+ from Polluted Groundwater by Insoluble Humic Acid/Tourmaline Composite Particles

Insoluble humic acid/tourmaline composite particles (IHA/TM) were prepared by combining inorganic tourmaline (TM) with the natural organic polymer humic acid (HA) and carbonizing them at 330 °C to study the removal characteristics and mechanism of Fe²⁺ and Mn²⁺. The results showed that the optimal ratio of TM to IHA is 2:3. When the temperature of the IHA/TM composite particles was 35 °C and the pH was 6, the adsorption of Fe²⁺ and Mn²⁺ by IHA/TM reached equilibrium at 240 min. The optimum dose of the adsorbent was 10 g/L, and the equilibrium adsorption capacities of Fe²⁺ and Mn²⁺ were 5.645 mg/g and 3.574 mg/g, respectively. The process of IHA/TM adsorption of Fe²⁺ and Mn²⁺ in water was spontaneous, endothermic and sustainable, and cooling was not conducive to adsorption. The pseudo-second order kinetic equation can well reflect the adsorption mechanism of IHA/TM on Fe²⁺ and Mn²⁺, and the Langmuir adsorption model better describes the isothermal adsorption behaviour. The material characterisation and adsorption experiments indicate that surface coordination and chemical precipitation are the main mechanisms of Fe²⁺ and Mn²⁺ removal by IHA/TM.     

Kinetics and Thermodynamics Studies for Cadmium (II) Adsorption onto Functionalized Chitosan with Hexa-Decyl-Trimethyl-Ammonium Chloride

A new adsorbent material was obtained by functionalization of chitosan with hexa-decyl-trimethyl-ammonium chloride and tested as an adsorbent for Cd(II) ions. Functionalization is due to the desire to improve the adsorbent properties of the biopolymer used for removal of metallic ions. Obtained material was characterized by FTIR (Fourier Transform InfraRed spectroscopy), SEM (Scanning Electron Microscopy) and EDX (Energy dispersive X-ray Spectroscopy). To prove the Cd(II) adsorption mechanism, we performed adsorption tests determining influence of biopolymer ratio, pH, contact time, temperature and Cd(II) initial concentration. Obtained experimental data were modeled using two kinetics models: pseudo-first-order and pseudo-second-order models. Cd(II) adsorption kinetics was better described by pseudo-second-order model. Further, experimental data were fitted using three different adsorption isotherms: Langmuir, Freundlich and Sips. The studied adsorption process is well described by the Sips adsorption isotherm, when the maximum adsorption capacity value is near the experimental one. Likewise, we evaluated the values of thermodynamic parameters which indicate that the studied process is an endothermic and spontaneous one, being a physical adsorption. Prepared adsorbent materials have a maximum adsorption capacity of 204.3 mg Cd²⁺ per gram at pH > 4.0 and 298 K. In addition, this material was reused for Cd²⁺ recovery for 20 times.     

Zero-Valent Iron Nanoparticles Remediate Nickel-Contaminated Aqueous Solutions and Biosolids-Amended Agricultural Soil

Nickel (Ni⁺²) accumulation in wastewater treatment sludge poses a potential environmental risk with biosolids-land application. An incubation experiment was conducted to evaluate the effect of nanoparticles of zero-valent iron (nZVI) on Ni⁺² sorption in biosolids-treated agricultural soils. Two application rates of biosolids (0, 5%, w/w) and four treatment levels (0, 1, 5, and 10 g/kg) of nZVI were examined, either separately or interactively. The results of this study showed significant differences in Ni⁺² sorption capacity between different nZVI treatments. The initial Ni⁺² concentration in biosolids-amended soil significantly affected Ni sorption in the soil treated with nZVI. The “H-shape” of sorption isotherm in nZVI-treated soil reflects strong interaction between the Ni concentration and the nZVI treatment, while the C-shape of sorption isotherm in biosolids-amended soil without the nZVI treatment indicates intermediate affinity for Ni⁺² sorption. Nickel retention in soil was increased with the increase of nZVI levels. The removal efficiency of Ni⁺² by nZVI from solution was increased with the increase of pH from 5 to 11 and reached a maximum of 99.56% at pH 11 and nZVI treatment of 10 g/kg. The Ni⁺² desorption rate decreased from 92 to 7, 4, and 1% with increasing nZVI treatment levels from 0 to 1, 5, and 10 g/kg, respectively, with a soil Ni⁺² concentration of 50 mg/L. The maximum adsorption capacity (𝑞_max) of 10 g/kg nZVI-treated soil was 333.3 mg/g, which was much higher than those from the other treatments of 0 (5 mg/g), 1 (25 mg/g), and 5 g/kg (125 mg/g). The underlying mechanism for Ni⁺² immobilization using nZVI in an aquatic environment is controlled by a sorption process, reduction of metal ion to zero-valent metal, as well as (co)precipitation. Moreover, increasing the nZVI treatment level in biosolids-amended soil significantly decreased bioavailable Ni⁺² concentrations in the soil.