Metal Adsorbent Research Articles

A robust aerogel incorporated with phthalocyanine-based porous organic polymers for highly efficient gold extraction

The gold recovery from electronic waste liquid is of great significance to the recycling of precious metals and environmental restoration. Adsorption method is the preferred technique for gold recovery, but its expansion and application prospects were often limited by the workability and recyclability of common solid powder adsorbents. Herein, a solid absorbent powder (phthalocyanine-based POP, TD-POP) was integrated into chitosan/polyethyleneimine aerogel (TD-POP@CS/PEI-2) via a facile cross-linking and lyophilization strategy. As expected, TD-POP@CS/PEI-2 possessed outstanding mechanical toughness and stability, demonstrating efficient and specific adsorption for Au (III). The maximum adsorption capacity was 2169 mg g−1, higher than most of the absorbents. TD-POP@CS/PEI-2 aerogel also exhibited fast kinetics (recovery efficiency of 81.3 % within 3 h), good selectivity (recovery efficiency of 98.35 % at 10 times concentration of Al3+, Zn2+, Cu2+ Cd2+, Co2+, Ni2+, Mn2+, and Cr6+ than Au ions) and reusability (eight times). Multiple characterizations revealed the adsorption mechanism, which implied that the excellent adsorption properties of the aerogel were ascribed to the electrostatic attraction between cationic aerogel and AuCl4− anion, coordination interaction between nitrogen-containing active sites and Au (III), and reduction of Au (III) by TD-POP@CS/PEI-2 aerogel. This work provides a valuable and promising strategy to design scalable and sustainable adsorbents for capture precious metals, also promotes the development of integral adsorbent for environmental remediation.

Utilization of rice husk ash as a potential catalyst for diatom growth and adsorbent for heavy metals in aquaculture systems

Many aquaculture environments suffer from significant silicon deficiencies and severe heavy metal contamination, posing substantial risks to both production and safety in aquaculture. This study aimed to assess the release of silicate from rice husk ash (RHA) and its impact on phytoplankton abundance and community composition, which are key factors affecting shellfish growth and survival. Additionally, the capacity of RHA to adsorb mercury (Hg2+) was examined using different modification methods. The results demonstrated that the concentration of dissolved silicate in seawater increased with higher RHA doses, reaching a maximum of 189.77 ± 45.61 μmol L−1 in the high RHA treatment (HR) with 1.0 g L−1 of RHA. Notably, the HR treatment group exhibited a significant increase in chlorophyll-a concentration for nano-phytoplankton (2–20 μm), with an up to eightfold rise in abundance compared to the control group. Moreover, the HR treatment resulted in a maximum diatom abundance of 4217 ± 741.98 cells L−1, benefiting diatom species such as Coscinodiscus sp., Nitzschia sp., and Cyclotella sp. These findings underscore the potential of RHA as a catalyst for diatom growth, which in turn supports the growth of shellfish. Furthermore, no concentrations of mercury (Hg), lead (Pb), cadmium (Cd), arsenic (As), copper (Cu), zinc (Zn), and chromium (Cr) were detected in any of the silicate enrichment treatments, confirming the safety of the RHA. The treatment of RHA with NaOH achieved an impressive removal efficiency of Hg2+, reaching up to 97.41 ± 0.33 %. This study highlights the promising application of agricultural waste RHA as a catalyst for diatom growth and an adsorbent for heavy metals in water systems relevant to aquaculture practices.

An insight into the utilization of high-sulfur green Saudi Arabian petcoke as an ecofriendly sorbent for enhanced simultaneous sequestration of heavy metal ions from industrial wastewaters

Developing effective and green sorbents for the sequestration of water pollutants has increased attention to safe and sustainable water generation. This study aimed to discover a new utilization and the ability of green, high-sulfur Saudi Arabian petcoke (SA-PET) for heavy metal ion uptake. The organic sulfur content and aromatic properties of SA-PET allowed for rapid and improved performance against various metal ions via strong complex formation reactions and cation-π interactions. Also, the effects of different analytical factors were carefully studied and optimized. At pH 6–7, the maximum recovery values of PbII, CuII, CdII, ZnII, MnII, NiII and CoII metal ions were 21.09–95.76%. The experimental results demonstrate single-layer adsorption at the binding sites on the petcoke’s surface, and they are in good agreement with the Langmuir model in explaining the adsorption process, which is driven by electrostatic interactions between the petcoke surface and the studied metal ions. The pseudo-second-order kinetics model fits the adsorption data for all the target metal ions well. Furthermore, the outstanding SA-PET's stability allowed for efficient extractions over the course of 10 successive runs with negligible loss in the metal recovery percentage. With extraction recoveries up to 96.6% and a relative standard deviation less than 5%, SA-PET's efficiency in removing the target metal ions from different industrial wastewater samples gives it excellent promise as a novel green sorbent for detoxifying heavy metals from aquatic life. In conclusions, our findings, SA-PET emerged as a viable substitute for traditional synthetic adsorbents of heavy metals, in keeping with the growing trend toward green adsorbents for more sustainable development.

Comparison of the Effectiveness of Calcined Chicken and Duck Eggshells as Zn Metal Adsorbent Using Atomic Absorption Spectrophotometric

Comparison of the Effectiveness of Calcined Chicken and Duck Eggshells as Zn Metal Adsorbent Using Atomic Absorption Spectrophotometric

Optimization of hydrochar synthesis conditions for enhanced Cd(II) and Pb(II) adsorption in mono and multimetallic systems

The characterisation of hydrochars derived from Sargassum biomass collected along the Mexican Caribbean coast reveals their favourable morphology and chemical composition for incorporating metal ions, including Cd(II) and Pb(II). Among the synthesized materials, HCS-3, produced at 180 °C with a 2 h residence time, exhibited superior yield, specific area, carbon content, and capacity for removing Cd(II) and Pb(II). Adsorption equilibrium studies demonstrate the presence of adsorption processes during Cd(II) and Pb(II) retention on HCS-3, with adsorption capacities slightly exceeding 140 and 340 mg g⁻1, respectively. Notably, HCS-3 shows a greater affinity for Pb(II) over Cd(II) when both elements are present concurrently. The physicochemical analysis through FTIR spectroscopy, functional group analysis, point of zero charge determination, SEM/EDS, and other techniques evidenced that HCS-3 possesses favourable characteristics to serve as a heavy metal adsorbent. These findings underscore the efficacy of hydrochars from Sargassum biomass in removing heavy metals, suggesting their potential as superior adsorbents compared to traditional or novel materials, and advising its possible versatility for other pollutants. Utilizing these hydrochars could mitigate the economic and environmental impact of Sargassum biomass by repurposing it for valuable applications.

Cationite synthesis using anthracene extracted from pyrolysis resin by-products: A sustainable approach for production of efficient metal adsorbent

Keeping sustainable waste management and sustainable economy in view, this study investigated the synthesis of a novel polymethyleneanthracene sulfoacid cationite, derived from anthracene extracted with high efficiency (97 % purity) from pyrolysis resin byproducts (a Ustyurt gas-chemical complex). The successful sulfonation of anthracene yielded a substantial amount of the desired product (22.96 g), with a notable reaction efficiency of 82 %. Infrared spectroscopy confirmed the structure of anthracene and its sulfonated derivative, revealing characteristic absorption bands consistent with those of aromatic compounds. Thermogravimetric analysis revealed the thermal stability of the material at temperatures up to 600 °C. The elemental composition, ascertained through EDS, quantified the elements as carbon (65.43 ± 0.05 %), oxygen (22.44 ± 0.05 %), sodium (4.13 ± 0.01 %), and sulfur (8.00 ± 0.01 %). SEM images revealed a highly porous material structure, which is advantageous for ion exchange applications, particularly metal adsorption. Compared to commercial KU-2–8 cationite, the synthesized material had a lower mass density (650–720 g/dm³), a higher humidity content (62.5 %), and a larger comparative size (4.8 cm³/g). The general static exchange capacitance was 475–490 mg-eqv/g, which is slightly lower than the commercial standard of 500–520 mg-eqv/g. These findings indicate that the synthesized cationite has promising potential for ion exchange applications because of its competitive physical and chemical properties.

The influence of multi-step modification method on the adsorption effect of alkali metal adsorbent in high temperature corrosive environment

In order to mitigate the serious high-temperature corrosion problem caused by gaseous alkali metal salts on the heating surface of boilers, the adsorption effect of kaolinite for alkali metal vapor stood out among many silicon-aluminum-based adsorbents. To improve the adsorption capacity of kaolinite for alkali metal vapor, a novel multi-step modification method was proposed in this reported work. The multi-step modification method consisted of the following four steps, which were pre-intercalation, replacement intercalation, multiple intercalation, and exfoliation, and it was found that the multi-step modification method resulted in the increase of the particle size, the expansion of the interlayer spacing, and the expansion of the porosity structure of kaolinite. The physicochemical analyses showed that the multi-step modification method made it easier to dehydrate kaolinite to produce metakaolinite. In addition, it was found that the multi-step modification method led to the generation of a new crystalline phase of kaolinite, which was formed by the dehydration and condensation of methanol and AlOH groups. It also led to the pre-removal of some of the hydroxyl groups in kaolinite. The insoluble sodium loading capacity of the multi-step modified kaolinite was enhanced by 64.47% and the insoluble potassium loading capacity was enhanced by 29.68% under the adsorption condition of 850 °C for 45 min. Therefore, the multi-step modification method enhanced the alkali metal vapor adsorption capacity of raw kaolinite under high-temperature environment, which laid a certain foundation for subsequent research in this field.

A thorough investigation into the adsorption behavior of sophorolipid-modified fly ash towards compound pollution of lead and tetracycline

Heavy metal ions and antibiotics were simultaneously detected in authentic water systems. This research, for the first time, employed synthesized sophorolipid-modified fly ash(SFA) to eliminate tetracycline(TC) and lead(Pb2+) from wastewater. Various characterization techniques, including SEM-EDS, FTIR, XPS, BET, and Zeta, were employed to investigate the properties of the SFA. The results showed that the sophorolipid modification significantly improved the fly ash's adsorption capacities for the target pollutants. The static adsorption experiments elucidated the adsorption behaviors of SFA towards TC and Pb2+ in single and binary systems, highlighting the effects of different Environmental factors on the adsorption behavior in both types of systems. In single systems, SFA exhibited a maximum adsorption capacity of 128.96 mg/g for Pb2+ and 55.57 mg/g for TC. The adsorption of Pb2+ and TC followed pseudo-second-order kinetics and Freundlich isotherm models. The adsorption reactions are endothermic and occur spontaneously. SFA demonstrates varying adsorption mechanisms for two different types of pollutants. In the case of Pb2+, the primary mechanisms include ion exchange, electrostatic interaction, cation-π interaction, and complexation, while TC primarily engages in hydrogen bonding, π-π interaction, and complexation. The interaction between Pb2+ and TC has been shown to improve adsorption efficiency at low concentrations. Additionally, adsorption-desorption experiments confirm the reliable cycling performance of modified fly ash, highlighting its potential as a cost-effective and efficient adsorbent for antibiotics and heavy metals.

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.

Efficient adsorption of lead and copper from water by modification of sand filter with a green plant-based adsorbent: Adsorption kinetics and regeneration

In this study, pomegranate seed waste (PSW) was added into sand filter (SF) to increase removal efficiency of Lead (Pb(II)) and Copper (Cu(II)) from polluted water. The performance of PSW was compared with activated carbon (AC) as a typical adsorbent. Based on the SEM, EDX, FTIR, XRD, BET and proximate analyses, PSW had porous structure with specific surface area of 2.76 m2/g and active compounds which suggested PSW as an appropriate adsorbent for heavy metals (HMs) adsorption. According to the batch experiments, SF without treatment could only remove 46% and 35% of Pb(II) and Cu(II), respectively. These numbers increased to 88% and 75% for Pb(II) and Cu(II) by adding 3 g/kg PSW to the SF, respectively under the optimal conditions of HMs initial concentrations = 100 mg/L, pH = 7 and contact time = 60 min. The adsorption kinetic and isotherm followed the pseudo-first-order and Langmuir models, respectively indicating that mainly physisorption was involved in the HMs adsorption process of PSW. Based on the column experiments (flow rate = 62.5 mL/min), the Pb(II) and Cu(II) removal increased from 14% to 60% and 10%–55%, respectively after 5 pore volumes (40 min) by adding 3 g/kg PSW to the SF. Breakthrough curves matched better with Thomas mode rather than Adam's Bohart proving Langmuir adsorption isotherm. Our finding suggested modification of SF with PSW is a promising approach for efficient removal of HMs from water.

Carbonate Hydroxyapatite - A Multifunctional Bioceramics with Non-Medical Applications

Carbonate hydroxyapatite is the common derivative of hydroxyapatite found in living systems. It is the building block of most hard tissues, including the teeth and bones. A vast majority of the applications of this versatile material focus on its biomedical applications, which is attributable to its closeness to biological apatites. Hydroxyapatite is a strong precursor to carbonate apatite in nature, and many experiments show that both are similar in a few respects. A significant divergence point is carbonate's obvious impact on its physicochemical properties and concomitant applications. The inclusion of carbonate ions into the lattice of hydroxyapatite results in morphological and physicochemical changes that vary with the method of synthesis and extent of substitution. The unique crystal structure, improved surface area, and porous morphology of carbonate hydroxyapatites also make it useful for catalysis and environmental remediation as adsorbents for heavy metals. This review briefly examines carbonate hydroxyapatite, its synthesis, its modification, and its characterization. It also highlights its biomedical applications while drawing attention to its non-medical potential.

3D Spongin Scaffolds as Templates for Electro-Assisted Deposition of Selected Iron Oxides.

The skeletons of marine sponges are ancient biocomposite structures in which mineral phases are formed on 3D organic matrices. In addition to calcium- and silicate-containing biominerals, iron ions play an active role in skeleton formation in some species of bath sponges in the marine environment, which is a result of the biocorrosion of the metal structures on which these sponges settle. The interaction between iron ions and biopolymer spongin has motivated the development of selected extreme biomimetics approaches with the aim of creating new functional composites to use in environmental remediation and as adsorbents for heavy metals. In this study, for the first time, microporous 3D spongin scaffolds isolated from the cultivated marine bath sponge Hippospongia communis were used for electro-assisted deposition of iron oxides such as goethite [α-FeO(OH)] and lepidocrocite [γ-FeO(OH)]. The obtained iron oxide phases were characterized with the use of scanning electron microscopy, FTIR, and X-ray diffraction. In addition, mechanisms of electro-assisted deposition of iron oxides on the surface of spongin, as a sustainable biomaterial, are proposed and discussed.

Sustainable Lignin-Reinforced Chitosan Membranes for Efficient Cr(VI) Water Remediation.

The pollution of aquatic environments is a growing problem linked to population growth and intense anthropogenic activities. Because of their potential impact on human health and the environment, special attention is paid to contaminants of emerging concern, namely heavy metals. Thus, this work proposes the use of naturally derived materials capable of adsorbing chromium (VI) (Cr(VI)), a contaminant known for its potential toxicity and carcinogenic effects, providing a sustainable alternative for water remediation. For this purpose, membranes based on chitosan (CS) and chitosan/Kraft lignin (CS/KL) with different percentages of lignin (0.01 and 0.05 g) were developed using the solvent casting technique. The introduction of lignin imparts mechanical strength and reduces swelling in pristine chitosan. The CS and CS/0.01 KL membranes performed excellently, removing Cr(VI) at an initial 5 mg/L concentration. After 5 h of contact time, they showed about 100% removal. The adsorption process was analyzed using the pseudo-first-order model, and the interaction between the polymer matrix and the contaminant was attributed to electrostatic interactions. Therefore, CS and CS/KL membranes could be low-cost and efficient adsorbents for heavy metals in wastewater treatment applications.

High adsorption of Cu(II) in novel thiacalix[4]arene/acrylic polymer/diatomite fast fabricated by electron beam irradiation: Controllable microstructures, adsorption performance and mechanism

Chemical grafting of calix[4]arene is a common method to prepare high-performance calix[4]arene adsorbents for heavy metals, however, the chemical grafting process consumes much time and a large amount of heating energy due to the tedious steps. Herein, a thiacalix[4]arene/acrylic polymer/diatomite (TC4A/PAA/diatomite) adsorbent was fast fabricated by electron beam irradiation induced grafting, polymerization and crosslinking technique only in one-pot for the removal of Cu(II) as an important form of heavy metal pollution. Characterization by Fourier transform infrared (FTIR) spectra, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), diffuse reflectance UV–visible spectra and positron annihilation lifetime spectra (PALS) disclosed that the eco-friendly and low-cost TC4A/PAA/diatomite irradiated at 90 kGy namely TC4A/PAA/diatomite (90 kGy) with strong complexing ability owing to many functional groups such as carboxyl, hydroxyl etc in it. The effects of electron beam irradiation dose, initial solution pH, and initial concentration of Cu(II) on the adsorption performance of TC4A/PAA/diatomite were investigated. The isotherm adsorption data of Cu(II) in TC4A/PAA/diatomite (90 kGy) are more suitable for the Langmuir model with the maximum adsorption capacity of 123.30 mg/g. In addition, the bifunctional TC4A/PAA/diatomite (90 k Gy) can efficiently remove Cu(II) and display excellent reusability properties. The adsorption mechanism was further analyzed by FTIR, SEM, X-ray photoelelctron spectroscopy (XPS), diffuse reflectance UV–visible spectra and PALS. This study provides a fast, efficient and eco-friendly synthesis method of calix[4]arene adsorbent, conducing to the design of material innovation. Meanwhile, TC4A/PAA/diatomite (90 kGy) has potential application prospects in the treatment of practical Cu(II) contaminated wastewater.

Modification of Coal Fly Ash Waste into Manganese-Oxide-Coated-Zeolite (MOCZ) to Adsorb Heavy Metal Ions Ni2+

High consumption of coal as a source of electrical energy in Indonesia has resulted in piles of waste from coal burning, namely fly ash, which can damage the environment and harm health. Fly ash contains main oxides, namely silica (SiO2) and alumina (Al2O3), whose components are similar to zeolite, so they can be synthesized into zeolite-like material (ZLM) which can be used as an adsorbent for heavy metal Ni2+. Therefore, this research discussed the characterization of manganese-oxide-coated-zeolite (MOCZ) from fly ash waste as a heavy metal adsorbent. The research procedure consisted of preparation, purification, and activation stage of fly ash to obtain fly ash that is free from impurities, the stage of making sodium silicate and sodium aluminate, and zeolite synthesis. The resulting zeolite was then coated with manganese oxide to expand the surface area of the zeolite and increase the ability of zeolite to adsorb heavy metal Ni2+. The research results showed that fly ash waste that was coated with manganese oxide can adsorb heavy metal Ni2+. The adsorption of the Ni2+ metal ion solution by zeolite with MOCZ modification is in line with the pseudo-second-order kinetic and Langmuir isotherm.

Facile synthesis of a novel, efficient, reusable inorganic adsorbent from volcanic rock powder wastes and its application for the removal of dyes and metals from water

A new, efficient, and reusable inorganic adsorbent (NP.F) was easily synthesized using volcanic rock powder wastes (NP) as a precursor, with the synthesis of NP.F carried out at 550 ºC and with a ratio of NaOH (alkalinizing) and sample NP equal to 1. The samples were used in batch adsorption to uptake Ag+(aq.), Cu2+(aq.), acid green 16 (AG 16), and acid red 97 (AR 97) from aqueous solutions at pH 6.53, 5.98, and 2.3, respectively. NP and NP.F were characterized by different analytical techniques, such as XRD, FTIR, BET, TGA/DTG, etc. The adsorption kinetic carried out at 298 K for dye solutions with concentrations ranging from 50 to 200 mg L−1 and metals from 10 to 100 mg L−1 showed that data fit the pseudo-second-order mathematical model with rapid sorption and process equilibrium was reached after 30 min for dyes and 40 min for metal ions. The Sips model proved adequate to represent the adsorption isotherms of metallic ions and the dye AR 97, while the BET model represented the isotherms of the dye AG 16. The NP.F sample showed notable adsorption capacity for all the contaminants studied; for example, the adsorption capacity of the dye AR 97 was 295 mg g−1, while that of the Ag+ ion was 93 mg g−1. Besides, the adsorption of Cu2+(aq.) ion, dyes AG 16, and AR 97 were endothermic, while the adsorption of Ag+(aq.) was exothermic. Furthermore, even after numerous subsequent adsorption cycles, the NP.F sample maintained a high reusability, suggesting that the sample is qualified to be an adsorbent for removing contaminants from liquid effluents. In conclusion, NP.F could be easily converted into an efficient inorganic adsorbent for colorants and metals.

Highly efficient adsorption and removal of Cd(II) from wastewater by mass synthesis of magnetically functionalized UiO-66 based on its high coordination advantage

The development of heavy metal adsorbent materials that combine high yield and high adsorption capacity is a challenging problem. In this study, we report a novel magnetic adsorbent (Fe3O4@UiO-66-Lcys) for the efficient removal of cadmium from wastewater. Among them, UiO-66 was loaded on the Fe3O4 core by solvothermal method, followed by loading a large amount of L-cysteine (Lcys) on its surface by amidation reaction. The material innovatively achieves a large and uniform loading of functionalized groups on the magnetic core, which is a strategy for targeted removal of heavy metals. The successful synthesis of the materials was confirmed by structural characterization such as FTIR, TGA, and XRD. Excitingly, the composite has excellent adsorption performance, with the maximum adsorption of Cd2+ by Fe3O4@UiO-66-Lcys of 430.89 mg/g at the temperature of 298 K, which is more than five times that of Fe3O4@UiO-66. According to the mechanism analysis, the large amount of –COOH on UiO-66 provided enough sites for the stable grafting of L-cysteine, which exposed a large number of –NH2, –COOH, and −SH groups on the surface of the material, and provided abundant adsorption sites for Cd2+ chelation. In addition, the structure of the adsorbed material remained stable, and the removal rate of Cd2+ was still above 90 % after five times of reuse. Therefore, Fe3O4@UiO-66-Lcys is a good adsorbent for the removal of Cd2+ from wastewater, which provides an idea for the development and creation of high-yield, high-efficiency, and reusable green adsorbents.

Synthesis of Chitosan Silica Membrane from Petung Bamboo (<i>Dendrocalamus asper</i>) Leaves and Its Application as Pb(II) Metallic Adsorbent

Membrane synthesis through a phase inversion method using chitosan and sodium silicate solutions has been conducted. This research aims to characterize the silica chitosan membrane (SCM) of petung bamboo leaves and determine the synthesized product's adsorption capacity for Pb(II) ions. The XRF characterization showed the silica content of petung bamboo leaves with a percentage of 78.03%. SEM analysis before adsorption is around 13.0 μm, and the pore diameter after adsorption is around 9.7 μm. The results of adsorption analysis of Pb(II) metal using AAS showed that the SCM variation A at an initial concentration of 10.0000 ppm Pb(II) metal adsorbed was 9.8101 ppm, and at an initial concentration of 25.0000 ppm Pb(II) metal was 22.3421 ppm. The variation B at an initial concentration of 10.0000 ppm Pb(II) metal adsorbed was 9.8870 ppm and at an initial concentration of 25.0000 ppm Pb(II) metal adsorbed was 23.5806 ppm. The variation C at an initial concentration of 10.0000 ppm Pb(II) metal adsorbed was 9.9639 ppm, and at an initial concentration of 25.0000 ppm Pb(II) metal was 24.1855 ppm. The results of this research conclude that the highest SCM adsorption power is variation C (2%:22.95%) with a percentage of 99.63%.

Efficient Immobilization of heavy metals using newly synthesized magnetic nanoparticles and some bacteria in a multi-metal contaminated soil.

Simultaneous application of modified Fe3O4 with biological treatments in remediating multi-metal polluted soils, has rarely been investigated. Thus, a pioneering approach towards sustainable environmental remediation strategies is crucial. In this study, we aimed to improve the efficiency of Fe3O4 as adsorbents for heavy metals (HMs) by applying protective coatings. We synthesized core-shell magnetite nanoparticles coated with modified nanocellulose, nanohydrochar, and nanobiochar, and investigated their effectiveness in conjunction with bacteria (Pseudomonas putida and Bacillus megaterium) for remediating a multi-metal contamination soil. The results showed that the coatings significantly enhanced the immobilization of heavy metals in the soil, even at low doses (0.5%). The coating of nanocellulose had the highest efficiency in stabilizing metals due to the greater variety of surface functional groups and higher specific surface area (63.86 m2 g-1) than the other two coatings. Interestingly, uncoated Fe3O4 had lower performance (113.6 m2 g-1) due to their susceptibility to deformation and oxidation. The use of bacteria as a biological treatment led to an increase in the stabilization of metals in soil. In fact, Pseudomonas putida and Bacillus megaterium increased immobilization of HMs in soil successfully because of extracellular polymeric substances and intensive negative charges. Analysis of metal concentrations in plants revealed that Ni and Zn accumulated in the roots, while Pb and Cd were transferred from the roots to the shoots. Treatment Fe3O4 coated with modified nanocellulose at rates of 0.5 and 1% along with Pseudomonas putida showed the highest effect in stabilizing metals. Application of coated Fe3O4 for in-situ immobilization of HMs in contamination soils is recommendable due to their high metal stabilization efficiency and suitability to apply in large quantities.

Design, preparation, and performance of different adsorbents based on carboxymethyl chitosan/sodium alginate hydrogel beads for selective adsorption of Cadmium (II) and Chromium (III) metal ions

Developing cost-effective and efficient adsorbents for heavy metals in multicomponent systems is a challenge that needs to be resolved to meet the challenges of wastewater treatment technology. Two adsorbents were synthesized, characterized, and investigated for the removal of Cd2+ and Cr3+ as model heavy metals in their single and binary solutions. The first adsorbent (ACZ) was a nanocomposite formed of O-Carboxymethyl chitosan, sodium alginate, and zeolite. While, the other (ACL) contained ZnFe layered double hydroxides instead of the zeolite phase. Adsorbents were characterized using XRD, FTIR, SEM, and swelling degree analysis. For single heavy metal adsorption isotherms, data for both adsorbents was best fitted and indicated a multilayer adsorption nature. For binary adsorption, Langmuir model with interacting parameters showed the best results compared to other models for both pollutants. For single system, Avrami model was found to be the best model representing the adsorption kinetics data, which indicates that the mechanism of adsorption follows multiple kinetic orders that may change during duration of adsorption process. Numerous interaction mechanisms can occur between the heavy metals and functional groups in the synthesized hydrogels such as NH2, COOH, and OH groups leading to efficient adsorption of metal ions.