Super rapid removal of copper,cadmium and lead ions from water by NTA-silica gel

Copper (Cu²⁺), cadmium (Cd²⁺) and lead ions (Pb²⁺) are toxic to human beings and other organisms. In this study, a silica gel material modified with nitrilotriacetic acid (NTA-silica gel) was sensibly designed and prepared via a simple amidation procedure for the removal of Cu²⁺, Cd²⁺ and Pb²⁺ from water. The NTA-silica gels showed rapid removal performances for the three metal ions (Pb²⁺ (<2 min), Cu²⁺ and Cd²⁺ (<20 min)) with relatively high adsorption capacities (63.5, 53.14 and 76.22 mg g⁻¹ for Cu²⁺, Cd²⁺ and Pb²⁺, respectively). At the same concentration of 20 mg L⁻¹, the removal efficiencies of the three metals by the adsorbent ranged from 96% to 99%. The Freundlich and Langmuir models were utilized to fit the adsorption isotherms. The adsorption kinetics for the three metal ions was pseudo-second-order kinetics. The removal performance of the NTA-silica gels increased in a wide pH range (2–9) and maintained in the presence of competitive metal ions (Na⁺, Mg²⁺, Ca²⁺ and Al³⁺) with different concentrations. In addition, the NTA-silica gels were easily regenerated (washed with 1% HNO₃) and reused for 5 cycles with high adsorption capacity. This study indicates that the NTA-silica gel is a reusable adsorbent for the rapid, convenient, and efficient removal of Cu²⁺, Cd²⁺, and Pb²⁺ from contaminated aquatic environments.

A silica gel material modified with nitrilotriacetic acid (NTA-silica gel) was sensibly designed and prepared via a simple method for the super rapid removal of Cu²⁺, Cd²⁺ and Pb²⁺ from water.     

Acetylacetone functionalized magnetic carbon microspheres for the highly-efficient adsorption of heavy metal ions from aqueous solutions

Herein, Acac-C@Fe₃O₄, a magnetic carbon (C@Fe₃O₄) modified with acetylacetone (Acac), was first prepared and used as a solid-phase adsorbent for adsorbing some heavy metal ions from aqueous solution. The adsorbent was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometry (VSM) and BET studies. Some parameters affecting the adsorption and desorption processes were studied in Pb²⁺ solution, including sample pH, contact time, initial concentration, type and connection of the desorption solution. Absorption results showed that removal of Pb²⁺ was 100% under optimal conditions at an initial concentration of 10.0 mg L⁻¹. The adsorption mechanism conformed well to a pseudo-second order kinetic model. The adsorption capacity of the sorbent also showed promising results with Hg²⁺, Cr³⁺, Fe²⁺, Cd²⁺, Mn²⁺, Zn²⁺, Cu²⁺ and Pb²⁺, where maximum adsorption capacities reached 98.0, 151.2, 188.9, 202.2, 286.3, 297.2, 305.1 and 345.3 mg g⁻¹, respectively. The Acac-C@Fe₃O₄ microsphere material was successfully applied to the adsorption of heavy metal ions in aqueous solution.

Herein, Acac-C@Fe₃O₄, a magnetic carbon (C@Fe₃O₄) modified with acetylacetone (Acac), was first prepared and used as a solid-phase adsorbent for adsorbing some heavy metal ions from aqueous solution.     

Selective aptamer conjugation to silver-coated magnetite nanoparticles for magnetic solid-phase extraction of trace amounts of Pb2+ ions

Herein, a novel aptamer-functionalized magnetic adsorbent was developed and combined with magnetic solid-phase extraction (MSPE) for the specific enrichment of Pb²⁺ ions prior to flame atomic absorption spectrometric detection. First, silver-coated magnetite core–shell nanoparticles (Fe₃O₄@Ag MNPs) were synthesized by the chemical reduction of silver ions on the surface of magnetite nanoparticles. After that, the selective DNA aptamer against Pb²⁺ was conjugated on the surface of the synthesized nanoparticles to form aptamer-modified magnetic nanoparticles (Fe₃O₄@Ag-APT). The characterization of the prepared adsorbent was performed through SEM imaging, XRD, FT-IR, EDX, and DRS instruments. The influence of the various experimental parameters on the adsorption and desorption steps in MSPE was investigated via Taguchi experimental design to optimize different parameters. Under the optimized conditions, the Pb²⁺ calibration graph was linear in the range of 33–1000 μg L⁻¹. The relative standard deviation (RSD%) of the method for six replicates containing 100 μg L⁻¹ of Pb²⁺ ions was 0.34%. Furthermore, the limit of detection (LOD) and the limit of quantification (LOQ) were 10 μg L⁻¹ and 33.3 μg L⁻¹, respectively. Finally, the applicability of the proposed method was successfully confirmed by preconcentration and determination of trace amounts of Pb²⁺ ions in tap and seawater samples. We showed a proof of concept for Fe₃O₄@Ag-APT as an efficient bio-adsorbent, offering a promising strategy for the specific binding/removal of toxic heavy metal ions.

Herein, a novel aptamer-functionalized magnetic adsorbent was developed and combined with magnetic solid-phase extraction (MSPE) for the specific enrichment of Pb²⁺ ions prior to flame atomic absorption spectrometric detection.     

Novel magnetically separable anhydride-functionalized Fe3O4@SiO2@PEI-NTDA nanoparticles as effective adsorbents: synthesis,stability and recyclable adsorption performance for heavy metal ions

In this paper, a novel adsorbent, Fe₃O₄@SiO₂@PEI-NTDA, was first prepared by the immobilization of an amine and anhydride onto magnetic Fe₃O₄@SiO₂ nanoparticles with polyethylenimine (PEI) and 1,4,5,8-naphthalenetetracarboxylic-dianhydride (NTDA) for the removal of heavy metal ions from aqueous solutions. The structure of Fe₃O₄@SiO₂@PEI-NTDA was systematically investigated; the results confirmed that amine and anhydride groups were successfully covalently grafted onto the surface of Fe₃O₄@SiO₂, which showed a homogenous core–shell structure with three layers of about 300 nm diameter (Fe₃O₄ core: 200 nm, nSiO₂ layer: 20 nm, and PEI-NTDA layer: 20 nm). The adsorption performance of Fe₃O₄@SiO₂@PEI-NTDA NPs was evaluated for single Pb²⁺ and coexisting Cd²⁺, Ni²⁺, Cu²⁺, and Zn²⁺ ions in an aqueous solution in a batch system. The amine and anhydride groups may have a synergistic effect on Pb²⁺ removal through electrostatic interactions and chelation; Fe₃O₄@SiO₂@PEI-NTDA NPs exhibited preferable removal of Pb²⁺ with maximum adsorption capacity of 285.3 mg g⁻¹ for Pb²⁺ at a solution pH of 6.0, adsorbent dosage of 0.5 g L⁻¹, initial Pb²⁺ concentration of 200 mg L⁻¹ and contact time of 3 h. The adsorption mechanism conformed well to the Langmuir isotherm model, and the adsorption kinetic data were found to fit the pseudo-second order model. Fe₃O₄@SiO₂@PEI-NTDA NPs could be recovered easily from their dispersion by an external magnetic field and demonstrated good recyclability and reusability for at least 6 cycles with a high adsorption capacity above 204.5 mg g⁻¹. The magnetic adsorbents showed high stability with a weight loss below 0.65% in the acid leaching treatment by 2 M HCl solution for 144 h. This study indicates that Fe₃O₄@SiO₂@PEI-NTDA NPs are new promising adsorbents for the effective removal of Pb²⁺ in wastewater treatment.

A magnetically separable adsorbent, anhydride-functionalized Fe₃O₄@SiO₂@PEI-NTDA, was successfully constructed for removal of heavy metal ions from aqueous solution.     

Comparative study on synchronous adsorption of arsenate and fluoride in aqueous solution onto MgAlFe-LDHs with different intercalating anions

In this study, a series of MgAlFe-LDHs (Cl⁻, NO₃⁻, intercalation, and calcined products of a CO₃²⁻ interlayer) was synthesized and used for adsorption of arsenate and fluoride in individual contaminants and coexisting pollutant systems. Effects of various factors such as initial pH of solution, dosage of materials, coexisting ions, contact time, and initial pollutant concentrations were evaluated. Experimental results showed that different intercalating anions had a significant effect on adsorption performance of arsenate and fluoride in water. The adsorption of arsenate and fluoride on MgAlFe-CLDH, MgAlFe–Cl-LDH or MgAlFe–NO₃-LDH can be described by different adsorption isotherm equations. During the simultaneous removal process, arsenate and fluoride competed for adsorption sites of the adsorbent materials, and the fluoride ions had advantages in the competitive adsorption on MgAlFe–Cl-LDH and MgAlFe–NO₃-LDH. MgAlFe–NO₃-LDH was used to adsorb arsenate and fluoride in coexisting pollution systems (the concentration of each pollutant was 2 mg L⁻¹, the adsorbent dosage was 1.5 g L⁻¹). The remaining arsenic concentration was reduced to less than 10 μg L⁻¹ and the remaining fluoride ion concentration to below 20 μg L⁻¹ which meets the World Health Organization''s, EPA''s and China''s drinking water standards for arsenic and fluoride limits. A possible mechanism is discussed with support from further XRD, SEM, and XPS analysis of the materials after their adsorption.

During the simultaneous removal process, arsenate and fluoride competed for the adsorption sites of the adsorbent materials.     

Synthesis of MoS2 nanosheets for mercury speciation analysis by HPLC-UV-HG-AFS

Mercury species have aroused wide concern in the past several decades due to their high toxicity. However, it is still difficult to detect ultra-trace mercury species due to their biochemical transformation in complex samples. To establish a simpler and more sensitive method for pre-concentration and determination of trace mercury species, molybdenum disulfide (MoS₂) nanosheets with sulfur-rich characteristics and enlarged interlayer spacing were prepared by a hydrothermal method coupled with a sonication-assisted liquid exfoliation method and acted as solid-phase extraction adsorbent. The nano-MoS₂ had high adsorption capacity, fast adsorption rate and excellent selectivity towards mercury ions (Hg²⁺), methyl mercury (MeHg⁺) and ethyl mercury (EtHg⁺) in a wide pH range and complex matrices. And it could be easily regenerated by 4 mol L⁻¹ HCl and reused several times. After optimizing HPLC-UV-HG-AFS conditions, a great linearity (1.0–10.0 μg L⁻¹, R² = 0.999 for Hg²⁺, MeHg⁺ and EtHg⁺), lower detection limits (0.017, 0.037 and 0.021 ng mL⁻¹ for Hg²⁺, MeHg⁺ and EtHg⁺, respectively), relative standard deviations (<5%) and addition recoveries of the samples within 82.75–113.38% were observed. In summary, trace inorganic and organic mercury species in environmental and biological samples could be selectively enriched by the prepared nano-MoS₂ and efficiently seperated and detected by HPLC-UV-HG-AFS. The present study will help provide a better strategy for environmental monitoring and health assessment of mercury pollutants.

As-synthesized few-layered molybdenum disulfide nanosheets were used as solid-phase extraction absorbent for ultra-trace mercury speciation analysis by HPLC-UV-HG-AFS.     

Factors governing the competition between group IA and IB cations for monensin A: a DFT/PCM study

The affinity of monensin A to bind monovalent metal cations was evaluated by means of density functional theory (DFT) combined with polarizable continuum model (PCM) computations. The effect of various factors on complex formation between the monensinate A anion and group IA and IB metal ions was assessed. Competition between Na⁺ taken as a reference and monovalent metal cations was estimated using the Gibbs free energy for substituting the ligand-bound Na⁺ with its rival ions in the process [M⁺-solution] + [Mon⁻Na⁺] → [Mon⁻M⁺] + [Na⁺-solution] (M⁺ = Li⁺, K⁺, Rb⁺, Cs⁺, Cu⁺, Ag⁺ and Au⁺). The calculations revealed that the decrease in size of the cations accompanied by an increase of their accepting ability enhances the metal selectivity towards ligand donor atoms. In the gas-phase the affinity of monensinate A decreases in the order Cu⁺ > Li⁺ > Na⁺ > Au⁺ > Ag⁺ > K⁺ > Rb⁺ > Cs⁺. The complex formation can be manipulated by changing the solvent used. The polyether ionophore selectively binds Na⁺ ions in polar solvents but could become Li⁺ or Cu⁺-selective in low-polarity solvents.

The results obtained suggest that the metal selectivity of monensin can be modulated by changing the solvents used.     

Enhancing adsorption capacity and structural stability of Li1.6Mn1.6O4 adsorbents by anion/cation co-doping

Modifying the structure of Li_1.6Mn_1.6O₄ (LMO) to enhance its structural stability and adsorption capacity is an effective method to generate materials to recover Li⁺ ions from mixed solution. Herein, the co-doping of trace non-metal ion (S) and metal ion (Al) into Li_1.6Mn_1.6O₄ (LMO-SAl) is established and shows excellent Li⁺ adsorption capacity and Mn anti-dissolution properties. The adsorption capacity (when [Li⁺] is 6 mmol L⁻¹) is increased from 26.1 mg g⁻¹ to 33.7 mg g⁻¹. This is attributed to improved charge density via substitution of S at O sites, which facilitates the adsorption/desorption process. The Mn dissolution is also reduced from 5.4% to 3.0% for LMO-SAl, which may result from the stronger Al–O bonds compared to Li–O bonds that enhance the structural stability of the LMO. The ion-sieving ability of the co-doped material goes by the order of K_d (Li⁺ > Ca²⁺ > Mg²⁺ > Na⁺ > K⁺), indicating that Li⁺ can be efficiently separated from Lagoco Salt Lake brine. These results predict that lithium ions are effectively adsorbed from brine by the co-doped LMO material, which manifests the feasibility of lithium recovery and provides basic data for further industrial applications of adsorption.

Modifying the structure of Li_1.6Mn_1.6O₄ (LMO) to enhance its structural stability and adsorption capacity is an effective method to generate materials to recover Li⁺ ions from mixed solution.     

Synthesis of Fe3O4@PVBC–TMT nanoparticles for the efficient removal of heavy metals ions

Core–shell magnetic Fe₃O₄@PVBC–TMT (Fe₃O₄@polyvinylbenzyl chloride–trithiocyanuric acid) nanoparticles containing trithiocyanuric acid groups were fabricated and employed for the fast removal of heavy metals from an aquatic environment. The morphology, structure and properties of Fe₃O₄@PVBC–TMT nanoparticles were characterized by a series of modern analytical tools. The adsorption behavior of the Fe₃O₄@PVBC–TMT nanoparticles for heavy metals ions in aqueous solutions was investigated by batch experiments. The maximum removal capacities of the Fe₃O₄@PVBC–TMT nanoparticles toward Mn²⁺, Ni²⁺, Cu²⁺, Cd²⁺ and Pb²⁺ ions were 127.4, 146.6, 180.5, 311.5, and 528.8 mg g⁻¹, respectively. Importantly, it is found that Pb²⁺ ions can be completely and quickly removed by the Fe₃O₄@PVBC–TMT nanoparticles. The equilibrium was established within 6 min, and the removal efficiencies were found to be 99.9%, 99.8% and 99.5% for Pb²⁺ ions at the initial concentrations of 100 mg L⁻¹, 200 mg L⁻¹ and 300 mg L⁻¹, respectively. It is hoped that the core–shell magnetic Fe₃O₄@PVBC–TMT nanoparticles may find application in wastewater treatment.

Core–shell Fe₃O₄@PVBC–TMT nanoparticles were fabricated and served as a valid magnetic adsorbent for the removal of heavy metals ions.     

Co-adsorption of an anionic dye in the presence of a cationic dye and a heavy metal ion by graphene oxide and photoreduced graphene oxide

To investigate the adsorption behavior of contaminants with different adsorbents and co-adsorbates under identical conditions, the adsorption capacities of anionic orange II (OII) dye onto graphene oxide (GO) and photoreduced GO (PRGO) in a single-component system and in the presence of cationic methylene blue (MB) dye as well as heavy metal ion Pb²⁺ were explored. In this work, PRGO was prepared by solar light irradiation of a GO dispersion. GO and PRGO were characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, Raman spectroscopy, atomic force microscopy, scanning electron microscopy, and transmission electron microscopy. The adsorption isotherms of OII, MB, and Pb²⁺ onto GO and PRGO in single and binary systems have been studied and analyzed by the Langmuir model. In the single system, the adsorption capacity of OII on GO can be promoted from 8.4 mg g⁻¹ to 32.5 mg g⁻¹ after solar light irradiation. While the adsorption capacities of MB and Pb²⁺ are not affected by the photoreduction process. In the binary system, a marked synergistic effect for the adsorption of OII has been determined in the presence of both MB and Pb²⁺, where the adsorption capacity of OII on PRGO has been improved from 8.4 mg g⁻¹ to 295 mg g⁻¹ and 105 mg g⁻¹, enhancements of 35- and 12.5-fold, respectively. In contrast, the presence of OII leads to a mildly antagonistic effect on the adsorption of MB and Pb²⁺. These findings show that the adsorption of anionic dyes by graphene-based materials can be strongly improved in the presence of either cationic dyes or heavy metal ions, which will be of great value in practical applications.

The adsorption capacity of graphene oxide (GO) for orange II (OII) can be remarkably enhanced in the presence of methylene blue (MB) and Pb²⁺.     

Simple,selective detection and efficient removal of toxic lead and silver metal ions using Acid Red 94

Toward the goal of detecting toxic elements and removing them from drinking water, we report herein the utilization of Acid Red 94 (AR94) in sensing the hazardous metal ions in water. Among the various examined metal ions (Ag⁺, Pb²⁺, K⁺, Mn²⁺, Zn²⁺, La³⁺, Hg²⁺, Ca²⁺, Cd²⁺, Co²⁺, and Ni²⁺), the UV-visible absorption spectra showed high selectivity and sensitivity for toxic silver and lead metal ions in an aqueous solution. The observed absorption spectral changes and the rapid color changes confirm complex formation between AR94 and both Ag⁺ and Pb²⁺ metal ions. The emission measurements showed the significant fluorescence quenching of the singlet excited state of AR94 in the presence of Ag⁺ and Pb²⁺ metal ions suggesting the formation of an irradiative dye–metal complex under the prevailing experimental conditions. In order to remove the accumulated complexes of AR94 with silver metal ions, safe and harmless mesoporous titanium dioxide was utilized efficiently in removing the complexes with adsorption capacities of 91% at 30 minutes. These findings suggest a simple, fast and efficient method for both detecting silver in water, and removing the formed AR94–metal complexes in water. In addition, AR94 is shown to be a good sensor for the presence of Ag and Pb nanoparticles, NPs, in aqueous solution. The absorption and emission spectra of AR94 showed significant changes that may be rationalized by the strong electromagnetic coupling induced by NPs plasmonic effects. These findings render AR94 a sensitive and selective sensor and a visual indicator for the qualitative and quantitative detection of silver ions, lead ions and their nanoparticles.

Toward the goal of detecting toxic elements and removing them from drinking water, we report herein the utilization of Acid Red 94 (AR94) in sensing the hazardous metal ions in water.     

Electrochemical heavy metal removal from water using PVC waste-derived N,S co-doped carbon materials

The removal of heavy metal contaminants has aroused global attention due to water shortage and the lax control on the discharge of heavy metal pollutants. Capacitive deionization (CDI) has emerged as a robust, energy-/cost-efficient technique for water treatment. Herein, we reported the simple synthesis of N, S-co-doped carbon materials (NS-C) derived from PVC plastic wastes as CDI electrode materials for the efficient removal of heavy metal ions (HMIs). The NS-C exhibited a large specific surface area (∼1230 m² g⁻¹) and contained heavy heteroatom doping (∼4.55 at% N and ∼13.30 at% S). The CDI electrode fabricated using NS-C showed high removal efficiency (94–99%), high capacity (36–62 mg g⁻¹), and good regeneration capability for the adsorption of various kinds of low-concentration heavy metal ions (including Fe²⁺, Co²⁺, Ni²⁺, Cu²⁺, Pb²⁺, and Cd²⁺). Moreover, PVC plastic wastes that are heavily accumulated in the environment and extremely hard to be decomposed and recycled were applied as the carbon source in this study for the fabrication of NS-C, which further rendered the importance of our study in practically treating hazardous waste (HMIs) with waste (PVC plastic wastes) in a clean and efficient way.

N, S-codoped carbon materials derived from PVC plastic wastes were used for electrochemically removing heavy metal pollutants from water.     

Effect of different pyrolysis temperatures on physico-chemical characteristics and lead(ii) removal of biochar derived from chicken manure

Biochar derived from chicken manure, as an effective metal adsorbent, was prepared through a pyrolysis method at different pyrolytic temperatures (200, 400, 600, and 800 °C). The physicochemical characteristics of chicken manure biochar (CMB) and its lead (Pb²⁺) adsorption mechanisms were studied by batch adsorption experiments, DTA/TGA, XRD, SEM-EDS, FTIR and an analysis of the composition of their mineral ash. Results showed that the best-fit for the Pb²⁺ adsorption data was achieved using a Langmuir isotherm and a pseudo-second-order model. The maximum adsorption capacities of Pb²⁺ increased with increasing of pyrolytic temperatures of the CMB, being 180.21, 200.80, 239.59, and 242.57 mg g⁻¹, respectively, for CMB-200, CMB-400, CMB-600 and CMB-200. Although Pb²⁺ adsorption on CMB revealed that adsorption was controlled by multiple mechanisms, (e.g. surface complexation, ion exchange, surface precipitation, electrostatic attraction, physical adsorption, and co-precipitation), the ion exchange and surface precipitation played a dominant role in Pb²⁺ sorption. Using CMB for the removal of Pb from water is proposed as an effective, environmentally protective, novel approach.

Biochar derived from chicken manure, as an effective metal adsorbent, was prepared through a pyrolysis method at different pyrolytic temperatures (200, 400, 600, and 800 °C).     

Theoretical studies on carbon dioxide adsorption in cation-exchanged molecular sieves

The capture and storage of the greenhouse gas, CO₂, has attracted much interest from scientists in recent years. In this work, density functional theory (DFT) was used to study the adsorption of CO₂ in different cation-exchanged molecular sieves. The results show that for the monovalent metal (Li, Na, K, Cu) ion-exchanged molecular sieves (zeolite Y, ZSM-5, CHA and A), the adsorption capacities for CO₂ decrease in the order of Li⁺ > Na⁺ > K⁺ > Cu⁺. Cu⁺-exchanged zeolites are not suitable as adsorbents for CO₂. For the CO₂ adsorption capacities in different zeolites with the same exchanged cation, the adsorption energy decreases in the order of Y > A > ZSM-5 ≈ CHA for Li-exchanged zeolites, and ZSM-5 still has the lowest CO₂ adsorption energy for both Na- and K-exchanged zeolites. In the cation-exchanged Y zeolites with divalent metals (Be, Mg, Ca and Zn), the CO₂ adsorption performance increases in the order of Zn²⁺ < Be²⁺ < Ca²⁺ < Mg²⁺. Thus, Zn²⁺-exchanged zeolites are not suitable as adsorbents for CO₂.

Density functional theory was used to study the adsorption of CO₂ in cation-exchanged zeolite Y, ZSM-5, CHA and A. The adsorption energies and the interactions of cations on various zeolitic topologies towards CO₂ molecule was discussed.     

Preparation of terpyridine-functionalized paramagnetic nickel–zinc ferrite microspheres for adsorbing Pb(ii), Hg(ii), and Cd(ii) from water

A paramagnetic microsphere combining special functional groups may be one kind of the most promising methods for heavy metal adsorption, due to their specific separation capacity, selectivity and reusability. In this study, a novel terpyridine-based magnetic solid-phase adsorbent (TPY-M) is successfully constructed. The paramagnetic Ni_0.25Zn_0.75Fe₂O₄ microsphere (M) is synthesized and applied as a magnetic core, and is functionalized by terpyridine (TPY) groups. The naked magnetic core and TPY-M are characterized by vibration sample magnetism (VSM), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), and Fourier-transform infrared spectroscopy (FT-IR) techniques. Some parameters of the TPY-M samples are evaluated as potential adsorbents for heavy metal ions in various aqueous solutions. The adsorption capacities of TPY-M for Pb(ii), Hg(ii) and Cd(ii) were 64.75 mg g⁻¹, 33.94 mg g⁻¹ and 24.64 mg g⁻¹ under given conditions, respectively. In the case of Pb(ii), some influencing factors on the TPY-M adsorbent are investigated, including the pH, adsorption time, and ion concentrations. The adsorbent can be easily regenerated by HCl solution after use. The adsorbent revealed good adsorption performance in some real water samples.

A paramagnetic microsphere combining special functional groups may be one kind of the most promising methods for heavy metal adsorption, due to their specific separation capacity, selectivity and reusability.     

The use of acrylic yarn modified with amidoxime and carboxylate-containing polymer for lead removal from drinking water

Amidoxime and carboxylate-containing polymer adsorbents derived from acrylic yarn exhibit high adsorption capacity for lead(ii) (Pb²⁺) ions in water. The adsorption process follows pseudo-second-order kinetics and fits the extended Langmuir isotherm model with the maximum adsorption capacity of Pb²⁺ with 238 mg lead per gram of the fiber at room temperature. Endothermic (ΔH° = 20.3 kJ per mole), spontaneous, and with the increase in the entropy of Pb²⁺ adsorption was observed from the thermodynamic studies. Dynamic column adsorption experiments showed that the fiber can process 4.3 L of water spiked with 1 ppm of lead(ii) solution at a flow rate of 4.4 mL per min under the specified conditions. The selectivity of Pb²⁺ with the competitive metal ions showed varying results with highly selective for Pb²⁺ in a binary solution with sodium and calcium and varying degrees of competitiveness with transition metal ions. This efficient and easily prepared fiber adsorbent appears to be a promising new material for the remediation of lead-contaminated aquatic environments and potable waters.

Amidoxime and carboxylate-containing polymer adsorbents derived from acrylic yarn exhibit high adsorption capacity for lead (Pb²⁺) ions in water.     

Tinospora cordifolia derived biomass functionalized ZnO particles for effective removal of lead(ii), iron(iii), phosphate and arsenic(iii) from water

Owing to the vast diversity in functional groups and cost effectiveness, biomass can be used for various applications. In the present study, biomass from Tinospora cordifolia (TnC) was prepared and grafted onto the surface of ZnO particles following a simple method. The TnC functionalized ZnO particles (ZnO@TnC) were characterized and exhibited excellent adsorption properties towards Pb²⁺ (506 mg g⁻¹), Fe³⁺ (358 mg g⁻¹) and PO₄³⁻ (1606 mg g⁻¹) and the Fe³⁺ adsorbed ZnO@TnC adsorbs AsO₂¹⁻ (189 mg g⁻¹); the metal ions and anions were analyzed by ICP and IC. For reuse of ZnO@TnC, a desorption study was successfully carried out using NaOH and EDTA for PO₄³⁻ and Pb²⁺, respectively; Fe³⁺ was further used for adsorption of As(iii). The adsorption fits well with the Langmuir adsorption isotherm model and the adsorption kinetic data are best fitted with a pseudo-second-order equation. The system developed may be useful for treatment of waste water and industrial effluents.

Owing to the vast diversity in functional groups and cost effectiveness, biomass can be used for various applications.     

Metal ion size profoundly affects H3glyox chelate chemistry

The bisoxine hexadentate chelating ligand, H₃glyox was investigated for its affinity for Mn²⁺, Cu²⁺ and Lu³⁺ ions; all three metal ions are relevant with applications in nuclear medicine and medicinal inorganic chemistry. The aqueous coordination chemistry and thermodynamic stability of all three metal complexes were thoroughly investigated by detailed DFT structure calculations and stability constant determination, by employing UV in-batch spectrophotometric titrations, giving pM values (pM = −log[Mⁿ⁺]_free when [Mⁿ⁺] = 1 μM, [L] = 10 μM at pH 7.4 and 25 °C) – pCu (25.2) > pLu (18.1) > pMn (12.0). DFT calculated structures revealed different geometries and coordination preferences of the three metal ions; notable was an inner sphere water molecule in the Mn²⁺ complex. H₃glyox labels [^52gMn]Mn²⁺, [⁶⁴Cu]Cu²⁺ and [¹⁷⁷Lu]Lu³⁺ at ambient conditions with apparent molar activities of 40 MBq μmol⁻¹, 500 MBq μmol⁻¹ and 25 GBq μmol⁻¹, respectively. Collectively, these initial investigations provide insight into the effects of metal ion size and charge on the chelation with the hexadentate H₃glyox and indicate that further investigations of the Mn²⁺–H₃glyox complex in ^52g/55Mn-based bimodal imaging might be worthwhile.

The bisoxine hexadentate chelating ligand, H₃glyox was investigated for its affinity for Mn²⁺, Cu²⁺ and Lu³⁺ ions; all three metal ions are relevant with applications in nuclear medicine and medicinal inorganic chemistry.     

Synthesis,structural characterization and Cu(ii) adsorption behavior of manganite (γ-MnOOH) nanorods

New alternatives for the removal of transition metal ions that present an environmental risk are required. The chemical adsorption of these ions on surfaces with chemisorbent properties represents a promising area of research. In this work, manganite (γ-MnOOH) nanorods were synthesized, with a surface area of 20.22 m² g⁻¹, pore size of 32.18 nm and pore volume of 0.1627 cm³ g⁻¹. After chemical and structural characterization of the manganite sample, it was evaluated as an adsorbent of Cu(ii) from aqueous solution. The equilibrium adsorption data were well fitted by the Langmuir isotherm, and the results indicated that the maximum adsorption capacity of Cu(ii) was 11.926 mg g⁻¹. Cu(ii) ion adsorption on the manganite surface is a spontaneous and exothermic process (ΔG°< 0 and ΔH°< 0). The negative value of ΔS° suggests the stability of the adsorption process without structural change at the manganite–aqueous solution interface. A scheme for chemisorption of Cu(ii) ions on the hydroxylated surface of manganite is proposed.

Manganite (γ-MnOOH) nanorods were synthesized and Cu(ii) adsorption on their hydroxylated surface was a spontaneous process (ΔG° < 0).     

Optimized synthesis of novel hydrogel for the adsorption of copper and cobalt ions in wastewater

Metal ions in wastewater endanger the environment and even human life. In this study, an optimized method was used to synthesize an excellent hydrogel to treat these metal ions. The samples were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA), and applied to treat the Cu(ii) and Co(ii) ions in wastewater. In the adsorption experiment, the influential factors such as pH, adsorption time, adsorbent dosage and concentration of heavy metal ions and regeneration efficiency were evaluated, and the adsorption kinetics, isotherms and thermodynamics were studied. The orthogonal optimization results show that the best condition for synthesis was when the degree of neutralization of acrylic acid (A) was 70%, the quantity of glucose (B) was 0.2 g, the quantity of chitosan (C) was 0.05 g, and the quantity of initiator (D) was 0.03 g. The influence of the four factors was in the order D > B > C > A. The adsorption performance was optimal under neutral conditions and the dosage of 0.02 g adsorbent was chosen as the best. Experiments show that the composite hydrogels exhibited excellent performance under optimal conditions: at 20 °C and pH = 7, the adsorption capacity of 100 mg L⁻¹ of Cu(ii) by 0.01 g hydrogel was 286 mg g⁻¹. The adsorption process of heavy metal ions by hydrogels conforms to pseudo-second-order kinetics and Langmuir isotherm model, which indicate a spontaneous endothermic reaction. Moreover, after five cycles, the removal rates of Cu(ii) and Co(ii) were 81% and 74.8%, respectively.

Metal ions in wastewater endanger the environment and even human life. In this study, an optimized method was used to synthesize an excellent hydrogel to treat these metal ions.