Cd Ions Research Articles

PERFORMANCE OF FREE WATER SURFACE FLOW CONSTRUCTED WETLAND FOR LEAD AND CADMIUM IONS REMOVAL USING AZOLLA PINNATA PLANT

Phytoremediation is the ability of some plants to bio accumulate, decompose, or transformation of pollutants in soils, water, or air. In the current study, an effort is made to study the effectiveness of free-floating plants to treat simulated industrial wastewater polluted with Lead and Cadmium ions using Azolla Pinnata plant in a lab condition. Free water surface flow constructed wetland were fed with simulated Cd and Pb ions in different concentrations (5, 10 and 20) mgl-1. Different operating conditions were studied such as; pH, dissolved oxygen, electrical conductivity, temperature, and sodium adsorption ratio to find out the possibility of using treated wastewater for irrigation. Results showed that, Azolla plant had a higher removal efficiency to extract Lead ions (90.1%, 86.67%, and 81.3%) than Cadmium (79.3%, 78.4%, and 69.7%) when the initial concentration is (5, 10, 20) mgl-1 respectively, during 5 days. A slight reducing in pH (8.3 to 7.4) and dissolved oxygen (8.7 to 7.2) mgl-1 observed, all these values mentioned satisfied with the Iraqi standards and World Health Organization. From values of electrical conductivities (250- 750) (µScm-1) and the sodium adsorption ratios (0- 10) it was found that treated wastewater falls into class C2S1 which mean that water has good quality and can be used to irrigate moderately salt-tolerant crops on soils with good permeability.

Chemical modification of Pinus walliichiana sawdust: Application in membrane system for efficient purification of groundwater containing Cd(II) and Ni(II)

In the Sargodha region of Pakistan, the concentrations of Cd(II) and Ni(II) ions are very high as compared to WHO and US EPA standards and may be one of the leading reasons for water-borne diseases in the population of this area. In the current research work, an eco-friendly, low-cost, effective, and reusable filter membrane system is developed. The cellulose sawdust of Pinus walliichiana (PWC) was treated with succinic anhydride to form Pinus walliichiana cellulose succinate (PWCS) and finally converted to sodic form (PWCS-Na) by treating with saturated sodium bicarbonate. The PWCS and PWCS-Na as obtained were characterized using FTIR, pHZPC, SEM, PXRD, and Brunauer–Emmett–Teller (BET) analysis. The BET surface area of the PWCS-Na was found to be 579.5 m2/g. Maximum sorption capacity values in the batch study for Cd(II) (235.2 ± 10.3 mg g−1) and Ni(II) (195.6 ± 15.2 mg g−1) were observed at 298 K, pH 6, sorbent dosage of 30 mg, and metal ion concentration of 70 mg/L. The filter membrane system was designed and employed for the purification of the flowing water system. Theoretical calculations show that 1 L of filter membrane containing 138.0 g of the adsorbent PWCS-Na can purify 532.8 L solution with Cd(II) concentration 70 mg/L and 278.2 L solution of Ni(II) with concentration 70 mg/L. The regeneration study proved the efficient reusability of sorbent after five cycles with a slight change in sorption capacity.

Ternary polymeric beads of chitosan-based polyaniline doped iron oxide used for removal of cadmium and lead ions from water: Kinetic, isotherm and mechanism studies

ABSTRACT In this study, the binary polymeric magnetic beads were synthesized successfully by one-pot polymerization of polyaniline (PA) doped magnetic iron oxide nanoparticles (MNPs) followed by chitosan (CTS) cross-linkage. The newly fabricated ternary magnetic beads (CTS@MPA) were applied to enhance the removal of Pb(II) and Cd(II) ions from the aqueous media. The prepared nanocomposite was characterized using Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and vibrating sample magnetometry (VSM). Adsorption experiments were carried out under optimum conditions. To evaluate the experimental data, the isotherm and kinetic models were conducted. The behavior of adsorption was assessed, and the coefficient of determination values demonstrated that the adsorption process best fitted the Freundlich model due to high values of R2 (0.957 & 0.981). The maximum adsorption capacity was obtained at 150.82 mg.g−1 and 169.21 mg.g−1 for Pb(II) and Cd(II) ions, respectively. Kinetic studies showed that adsorption follows a pseudo-second-order model (R2 = 0.952 & 0.985). Weber-Morris claims that intraparticle diffusion plays a significant role in the adsorption kinetics. Finally, the thermodynamic study is demonstrated, and the adsorption is endothermic, and the mechanism follows a physisorption pattern.

Synthesis of Porous Red Mud/Slag-Based Spherical Geopolymers for Efficient Methylene Blue and Ni2+ Removal from Water.

To reuse red mud and slag wastes as raw materials, a green type of porous spherical red mud/slag-based geopolymer (RSG) was synthesized by utilizing suspension curing and foaming techniques. Because methylene blue (MB) and nickel ion (Ni2+) were common and difficult to treat in wastewater, the adsorption characteristics of MB and Ni2+, as well as the phase and microstructure of the porous RSG spheres prior to and after adsorption, were thoroughly investigated. The porous RSG spheres showed a stable and mesoporous structure with a BET surface area of 31.36 m2/g. The spheres achieved the maximum removal efficiencies of 99.81% (MB) and 99.01% (Ni2+) at dosages of 16 and 10 g/L, respectively. The pseudo-second-order kinetic model and the Langmuir model could match the adsorption data of these spheres, with predicted maximum adsorption capacity (Qmax) values of 19.88 mg/g for MB and 12.39 mg/g for Ni2+, respectively. After three adsorption-desorption cycles, porous RSG spheres demonstrated good recycling capability with removal efficiencies of 98.10% (MB) and 54.60% (Ni2+). The spheres were also effective in adsorbing additional dyes (methyl orange (MO), crystal violet (CV), and malachite green (MG)) and heavy metal ions (Cd2+, Pb2+, Zn2+, and Cu2+). The spheres have potential use in water treatment.

Sugarcane Bagasse Based Adsorbents and their Adsorption Efficacy on Removal of Heavy Metals from Nakuru Industrial Wastewater: Optimization, Kinetic and Thermodynamic Aspects

Currently, researchers are seeking to reduce heavy metal contamination from the environment, using agricultural waste materials like rice husk, groundnuts shells among others. The study focused on the removal of Cu(II), Pb(II), Cd(II), Ni(II), and Cr(III) ions from aqueous solutions and Nakuru industrial wastewater using sugarcane bagasse (NSCB) and valorised bagasse ash (VSCB), as alternative low-cost agricultural waste bio-sorbents. To achieve this goal, sugarcane bagasse was collected from Nzoia sugar industry in western Kenya, while the valorised bagasse was obtained by heating sugarcane bagasse sample in a muffle furnace at 300°C for three hours. Furthermore, batch adsorption studies were performed, and the effects of several factors, i.e. adsorbent particle size, pH, contact time, initial heavy metal ions concentration and temperature were investigated to optimise the removal efficiency of Pb, Cu, Cd, Ni, and Cr. The optimal adsorption conditions were pH of 5.0, adsorbent dosage of 0.1 g and ≤ 150µm particle size, equilibrium time of 60 minutes and at 25 degrees Celcius. The removal kinetics of the metal ions onto both adsorbents fitted well with the pseudo-second-order model. The removal kinetics of the metal ions onto both adsorbents fitted well with the pseudo-second-order model. The adsorption of Pb2+ and Ni2+ onto NSCB fitted better with the Freundlich isotherm model, while Cd2+, Cu2+ and Cr3+ showed better fit for the Langmuir isotherm model. As for VSCB adsorbent, Cr3+ has a better fit with the Langmuir isotherm model whereas Pb2+, Ni2+, Cd2+, and Cu2+ fitted well on the Freundlich isotherm model. Freundlich constant’s (1/n) values and the separation factor (RL) from the Langmuir isotherm model indicate that the metal ions were favourably adsorbed onto the adsorbents. Langmuir isotherm model was used to estimate the maximum adsorption capacities (qmax) for Cu(II), Pb(II), Ni(II), Cd(II), and Cr(III). The negative free energy change (∆G) values revealed that adsorption process of the metal ions onto NSCB and VSCB was spontaneous. Fourier Transform Infrared Spectroscopy (FTIR) was used for characterization studies. Interactions with metal ions caused the frequencies of the active functional groups, –OH, C=O and C=C, on the bio-sorbent surfaces to shift to higher values. Therefore, sugarcane bagasse and valorised bagasse have demonstrated higher potential to remove relatively all selected heavy metals in the industrial wastewater at controlled pH.

Synthesis, Structural Characterization, Optical Properties, and Biological Potency of Co(II), Cu(II), and Cd(II) Complexes With Heterocyclic Thiosemicarbazide Ligand: Insights From Molecular Docking Studies

ABSTRACTA novel heterocyclic thiosemicarbazide ligand, [(Z)‐N‐(2‐oxoindolin‐3‐ylidene)nicotinohydrazide] (H2L), and its Co(II), Cu(II), and Cd(II) metal chelates were synthesized and characterized using a variety of analytical methods, including elemental analysis, FT‐IR, UV–Visible spectroscopy, EI‐mass, fluorescence spectroscopy, X‐ray powder diffraction, and TGA. The structures and geometries of the complexes were determined using these methods as [Co2(H2L)2Cl2(H2O)4]·2H2O, [Cu(H2L)2Cl2(H2O)2]·2H2O, and [Cd(H2L)2Cl2(H2O)2], all having octahedral geometry. The particulate diameters for [Co2(H2L)2Cl2(H2O)4]·2H2O, [Cu(H2L)2Cl2(H2O)2]·2H2O, and [Cd(H2L)2Cl2(H2O)2] were 192.68, 68.48, and 192.74 nm, respectively using Debye–Scherrer equation and FWHM approach. The corresponding FWHM values were 0.0078, 0.0217, and 0.0075, whereas the crystal strain was calculated as (ε) = 0.0018, 0.0056, and 0.0054, and the dislocation density (δ) as 2.69 × 10−5, 2.13 × 10−4, 2.69 × 10−5 Å−2. Quantum chemical calculations for the ligand and its solid metal complexes were carried out utilizing DFT with the DMOL3 module. Furthermore, the optical sensing response of the free ligand H2L to Co(II), Cu(II), and Cd(II) ions was investigated, revealing that the presence of these metal ions enhanced the fluorescence spectra of the ligand. Additionally, the antibacterial effects of these compounds, as well as their cytotoxicity in human cancer cells, were investigated. Compared to its metal complexes, the ligand, H2L exhibits increased antibacterial activity against various bacteria. Tests on HepG‐2 and MCF‐7 cells were conducted to evaluate the compounds' anticancer efficacy against the standard, Doxorubicin. The ligand, H2L, demonstrated greater cytotoxicity against the HepG‐2 cell line than its metal complexes. Docking experiments were conducted to assess the interaction of the ligand and its complexes with HepG‐2 (PDB ID: 2OH4) and MCF‐7 (PDB ID: 3W2S) cells, using the XP glide technique and Schrödinger suite software.

Preparation of Microelectrolysis Filler Using Coal Slag for the Removal of Hazardous Substances in Contaminated Water.

Presently, the utilization of gasification slag in the context of wastewater treatment is constrained. Furthermore, the presence of dye wastewater and wastewater containing hazardous metals represents a significant threat to human health. Accordingly, the present study prepared a microelectrolytic filler (MF) from gasification slag via a high-temperature roasting method and evaluated its degradation performance in water containing organic matter and harmful metal ions. The impact of varying preparation conditions, including initial solution pH and MF dose, on the degradation process was examined. The removal of methyl blue was found to be 92.21% at an initial pH of 2, a reaction time of 300 min and a dosage of 40 g L-1. The removal of Cu(II), Cd(II), and Pb(II) metal ions was 97.32, 96.58, and 99.38%, respectively, at an initial pH of 4, a reaction time of 180 min, and a dosage of 10 g L-1. Following five cycles, the MF process demonstrated continued efficacy in the removal of dyes and heavy metals from the wastewater. A mechanistic analysis revealed that the water treatment process is not a single adsorption process. Instead, it was found that organic macromolecules undergo chain-breaking reactions, while heavy metal ions undergo redox reactions. The wastewater treatment process comprises a number of distinct strategies, including electrochemical reactions, adsorption, flocculation, and precipitation. These findings illustrate the potential of a gasification slag green recycling approach to treat waste with waste, in alignment with the principles of sustainable development.

Adsorption isotherms and removal of lead (II) and cadmium (II) from aqueous media using nanobiochar and rice husk

Removal of Cd(II) and Pb(II) from aqueous solutions is a challenging task and the search for novel adsorbents is underway. This study examined the efficiency of nanobiochar (NB) and rice husk (RH) in the adsorption and removal of Cd(II) and Pb(II) from water. The effect of various physicochemical parameters such as initial pH, initial Cd and Pb concentration, adsorbent dosage, and contact time were tested. SEM/EDX images confirmed the adsorption of Pb and Cd with surface physical and chemical changes. The maximum Pb removal was noted at pH 6 using NB (96%) and at pH 8 for RH (90%), and the maximum Cd removal by NB was recorded at 8 pH (91%) and by RH at pH 6 (87%). The decline in adsorption intensity at lower pH suggested protonation of the adsorbent surface causing cation-cation repulsion. Most of the adsorption occurred within the initial 60 min. A continuous gradual increase in the adsorption with time suggested multilayer formation. Of the three isotherms, the Freundlich model fits the present data best, implying an infinite surface coverage and indicating the potential for multilayer adsorption of Pb and Cd on the surfaces of RH and NB adsorbents. In conclusion, this study highlights the promising potential of NB as a cost-effective adsorbent for the removal of Cd and Pb ions from aqueous solutions.

UV-modified biochar-Bacillus subtilis composite: An effective method for enhancing Cd(II) adsorption from water

The adsorption of Cd(Ⅱ) in sewage by single-modified biochar systems have limitations, whereas composite modification can enhance the efficiency. In this study, reed straw biochar and Bacillus subtilis were used as raw materials. UV radiation was employed to modify the biochar, and subsequently, Bacillus subtilis was loaded onto the biochar by adsorption, creating modified biochar composites. The Cd(II) adsorption performance and removal efficiency of these composites were then investigated. It was characterized by BET, SEM-EDS, FT-IR, XRD and ZETA potential analysis. Adsorption experiments were conducted under varying conditions (initial Cd(Ⅱ) concentration, UV radiation time, initial pH, etc.), with adsorption isotherms and kinetic models used. Results indicated that 24 hours UV radiation significantly enhanced adsorption performance, increasing the biochar’s surface area by 40 % and pore volume by 20 %, and introducing numerous pores and oxygen-containing functional groups to the biochar's surface. Significantly enhancing the saturation adsorption capacity for Cd(II) from 23.98 mg/g to 49.93 mg/g after UV- Modified biochar was loaded with Bacillus. Modified biochar composites performed better compared to single-modified biochar across different initial Cd(Ⅱ) concentrations, particularly in slightly alkaline environments. The primary adsorption mechanisms were chemical adsorption, such as ion exchange and surface precipitation. The synergistic effect of UV radiation and microbial loading significantly enhanced Cd(Ⅱ) adsorption efficiency. This study demonstrates that composite modification is a more efficient method, aiding in the removal of heavy metal ion Cd(Ⅱ) from water.

Indirect detection of lead(II), cadmium(II) and mercury(II) on a microfluidic electrophoresis chip.

Water environments contaminated by heavy metal ions present significant challenges because these pollutants do not degrade naturally, leading to their gradual bioaccumulation in animals and plants, which ultimately poses an insurmountable threat to human health. Therefore, rapid and accurate detection of heavy metal ions in water is of great significance for environmental protection and disease prevention. In this work, we developed a novel method based on microfluidic electrophoresis coupled with indirect chemiluminescence for the immediate detection of Cd(II), Pb(II) and Hg(II) heavy metal ions. The displacement of the Co(II) ions within the chemiluminescence mixture by the above migrating sample cations caused a measurable reduction in the background signal. The results showed that the detection limits of Cd(II), Pb(II) and Hg(II) ions under the best detection conditions were 5.83 × 10-8 M, 5.38 × 10-8 M and 2.09 × 10-8 M, respectively, which were 1-2 orders of magnitude lower than those of the indirect UV method and 1 order of magnitude lower than that of the indirect laser induced detection method. This method can provide a possibility for the rapid detection of multiple heavy metal ions in actual water environments.

Highly sensitive colorimetric detection of Cd(ii) based on silica sol modified with dithizone and cationic surfactant.

The cadmium ion (Cd2+) is highly poisonous and nondegradable and easily bioaccumulates through the food chain. Therefore, it is crucial to develop cost-effective chemical sensors for Cd2+ with fast response time, high selectivity, and very low detection limits. In this study, a colorimetric sensor for the determination of Cd2+ was fabricated by modifying silica sol with dodecyltrimethylammonium bromide (DTAB) and dithizone (DZ). Cd2+ formed a complex with DZ, changing the solution color immediately from purple to orange prior to detection using ultraviolet-visible spectrophotometry and a customized Cd analyzer for the precipitate. Under the optimum conditions, the developed Cd2+ sensor had a linear range of 0.01-0.25 mg L-1, a low limit of detection of 5.0 μg L-1, and outstanding repeatability. This sensor also showed good precision, with the relative standard deviations of less than 2.59% and 3.24% for the intra- and inter-day data, respectively. The proposed colorimetric method was successfully applied to determine Cd2+ in environmental water samples, and the results were comparable to those obtained using standard atomic absorption spectrometry. Moreover, quantitative analysis was conducted using the customized Cd analyzer to estimate the color intensity change, without requiring sophisticated scientific instruments. This colorimetric sensor can be used for the portable, cost-effective, and rapid on-site detection of Cd2+ in environmental water samples.

Carbon-based Nanocomposite Materials for Electrochemical Monitoring of Cadmium Ions

In the present era of science and technology, cadmium poisoning in humans is reported from several parts of the world and now it is a global health problem. Accumulation of cadmium in human organs and tissues, such as the liver, kidney, etc., leads to carcinogenic effects and toxicity to the organ system. Therefore, several efforts are being made to develop a monitoring system for cadmium metal ions in the environment. This review aimed to summarise the different carbon-composite materials-based electrochemical sensors reported to date for cadmium ions detection. The first section of this review provides a brief discussion on the source and harmful effects of cadmium ions, and the rest part includes different carbon (graphite, graphene, graphene oxide, carbon nanotubes, etc.)-based composite nanomaterials reported to date for the electrochemical detection of cadmium ions in different analytes. Carbon-based nanocomposite materials have been found to be very suitable for the detection of Cd(II) ions due to their boosted electron transportation and high surface, leading towards high sensitivity and high selectivity.

Hydroxamate Siderophores Intensify the Co-Deposition of Cadmium and Silicon as Phytolith-Like Particulates in Rice Stem Nodes: A Natural Strategy to Mitigate Grain Cadmium Accumulation.

Sequestration of cadmium (Cd) in rice phytolith can effectively restrict its migration to the grains, but how hydroxamate siderophore (HDS) affects phytolith formation within rice plants especially the fate of Cd and silicon (Si) remains poorly understood. Here, we found that the addition of HDS increased the content of dissolved Si and Cd in soil pore water as well as its absorption by the rice roots during the reproductive growth stage. HDS effectively trapped orthosilicic acid and Cd ions at the third stem nodes of rice plants via hydrogen bonds and chelation interactions, which then rapidly deposited on the xylem cell wall through hydrophobic interactions. Ultimately, Cd was immobilized as phytolith-like particulates in the form of CdSiO3. Field experiments verified that Cd accumulation was significantly reduced by 46.4% in rice grains but increased by 41.2% in rice stems after HDS addition. Overall, this study advances our understanding of microbial metabolites enhancing the instinctive physiological barriers within rice plants.

Dechlorination of Hexachlorobenzene by Ni/Fe Bimetallic Nanoparticles and the Influence of Co-Existing Heavy Metal Ions

Hexachlorobenzene (HCB) is one of the most persistent environmental pollutants of global concern. Ni/Fe nanoparticles, with their small particle size, large surface area, and high reactivity, are a promising candidate for HCB degradation. In this work, we investigated the kinetics and products of the dechlorination of HCB by Ni/Fe nanoparticles and how the presence of heavy metal ions Cd(Ⅱ) and Zn(Ⅱ) influences the reaction. It is found that 400 μg/L HCB can be rapidly removed by 7.5 g/L Ni/Fe nanoparticles and the removal percentage reaches 99% in 48 h. The removal is facilitated by adsorption and sequential dechlorination of HCB, producing PCB, 1,2,3,4-TeCB, and 1,2,3-TCB as the main products, with 1,2,3,5/1,2,4,5-TeCB, 1,2,4-TCB, and 1,2-DCB as the minor products. The addition of heavy metal ions Cd(Ⅱ) and Zn(Ⅱ) does not significantly affect the removal rate of HCB but hinders the adsorption and degradation of the byproducts through competitive adsorption. Additionally, the concentration of both Cd(Ⅱ) and Zn(Ⅱ) decreases rapidly and achieves over 98% removal in 4 h. Our study reveals that Ni/Fe nanoparticles can remove HCB and heavy metals Cd(Ⅱ) and Zn(Ⅱ) concurrently, with the extent of HCB dechlorination reduced compared to that without heavy metal. These findings may inform the application of Ni/Fe nanoparticles in the treatment of water bodies and soil contaminated by both halogenated aromatics and heavy metal.

Utilization of waste PET-derived metal–organic framework grafted polyaniline composite for heavy metal adsorption from aqueous solution

In this research, we used waste polyethylene terephthalate (PET) bottles as a source to develop an iron-based MOF-supported polyaniline (Fe-MOF@PANI) composite, which was then applied for the adsorptive removal of cadmium (Cd(II)) and lead (Pb(II)) ions from aqueous environment. A comprehensive characterization of the Fe-MOF@PANI composite was conducted using several analytical techniques including FTIR, PXRD, SEM, EDX with mapping, and XPS analysis, which provided significant insights into its functionality, crystalline structure, surface morphology, and elemental composition. The synthesized Fe-MOF exhibited a spindle-shaped morphology that was evenly distributed over the surface of the PANI composite, as confirmed by SEM analysis. Additionally, the porous characteristics of the Fe-MOF@PANI composite were proven through BET analysis. The Fe-MOF@PANI composite exhibited remarkable adsorption efficiencies for selected metal cations, achieving adsorption capacities of 143.36 mg/g and 258.59 mg/g for Cd(II) and Pb(II) ions, respectively. The findings of the isotherm and kinetic studies demonstrated that the adsorption process fitted well with Langmuir and pseudo-second-order kinetics, indicating that adsorption of both metal cations occurs in a monolayer formation and includes chemisorption mechanisms, respectively. This research paves the way for further development and application of post-functionalized PET-derived MOF adsorbents to remove Cd(II) and Pb(II) ions from water efficiently.

Electrochemical Detection of Cd2+ and Pb2+ in Wastewater by Amino C-dot-MOF/GCE

Carbon dots(C-dots) and metal-organic frameworks (MOFs) have found widespread applications in sensing, energy storage, and catalysis, yet their utilization in electrochemical sensing remains relatively limited. This study focuses on the preparation of C-dots/UiO-66-NH2 as a modified material on glassy carbon electrodes to detect cadmium and lead ions in water using electrochemical methods. The material was created by utilizing m-phenylenediamine as a C-dots source and amino-functionalized zirconium-based metal-organic frameworks, combining these two popular materials. The presence of amino groups in the structure facilitated the complexation with metal ions, providing an effective interface for metal ion adsorption. Under optimized deposition conditions, C-dots/UiO-66-NH2 demonstrated excellent linearity and low detection limits for metal ions (Cd2+ and Pb2+) within the concentration range of 30 to 180 μg l−1. The limits of detection (LOD) were LOD(Cd) = 2.16 μg l−1 and LOD(Pb) = 1.08 μg l−1 for individual detection, and LOD(Cd) = 2.62 μg l−1 and LOD(Pb) = 1.36 μg l−1 for simultaneous detection. These results highlight the suitability of C-dots/UiO-66-NH2 for the determination of Cd2+ and Pb2+ in water. Furthermore, the C-dots/UiO-66-NH2/GCE sensor exhibited robust immunity to interference and maintained detection stability, showcasing its potential for practical applications.

Heteronuclear coordination polymers with imidazole ligand: Synthesis, characterization and alcohol oxidation activities

Two new heteronuclear Cd(II)/Pd(II) coordination polymers, [Cd2(µ-im)2(Him)4Pd(µ-CN)4]n (1) and [Cd(Him)2Pd(µ-CN)4]n (2) (Him: imidazole), have been synthesized under different conditions and characterized using elemental analysis, thermal analysis, FT-IR and Raman spectroscopy, single-crystal and powder X-ray diffraction techniques.. In 1, the Cd(II) ions are bridged by imidazolate ligands to generate 1D chain structure. Neighbouring 1D chains were linked by [Pd(CN)4]2- ions to form 3D framework. In 2, the metal ions are bridged by cyanide ligands to generate 2D [Cd2Pd2(µ-CN)4]n network. Furthermore, catalytic peroxidative oxidation activity of catalysts 1 and 2 was examined on the oxidation of benzyl alcohol using tertiary-butyl hydroperoxide (t-BuOOH) as the oxygen source. The compound 1 exhibited over 90 % product conversion at 80 °C in 24-hour reaction time. In addition, the catalyst exhibited high selectivity towards benzaldehyde and no over-oxidation product (benzoic acid) was detected.

Immobilization of Pb, Cd, and Cr in contaminated soil around mining areas using Mg/Al LDH-zeolite and evaluation of maize growth

Abstract This study conducted simultaneous adsorption of Pb, Cd, and Cr ions using Mg/Al LDH-zeolite on contaminated soils from lead-zinc and tin mining areas. The optimal conditions were a 3% adsorbent-to-soil ratio, a 30-day incubation period, and 70% soil moisture. Characterization of the materials revealed that Mg/Al LDH-zeolite has superior physicochemical properties to natural zeolite, with a higher surface area and better adsorption capacity. Results indicated significant reductions in exchangeable heavy metal content: in lead-zinc mining area soil, exchangeable Pb decreased from 139.79 mg kg−1 to 10.95 mg kg−1, Cd−1 from 1.518 mg kg−1 to 0.533 mg kg−1, and Cr from 2.636 mg kg−1 to 0.461 mg/kg using Mg/Al LDH-zeolite. In tin mining area soil, exchangeable Pb decreased from 583.97 mg kg−1 to 48.22 mg kg−1, Cd−1 from 0.498 mg kg−1 to 0.122 mg kg−1, and Cr from 106.095 mg kg−1 to 38.038 mg/kg. Maize cultivation on post-adsorption soil showed improved growth performance, with plants exhibiting increased height and ear and reduced heavy metal accumulation in roots, shoots, and grains. Pb, Cd, and Cr concentrations in maize roots decreased significantly, with Pb reducing to 0.113 mg kg−1 in the lead-zinc area and 0.203 mg kg−1 in the tin area, Cd reducing to 0.061 mg kg−1 and 0.037 mg kg−1, respectively, and Cr reducing to 0.036 mg kg−1 and 0.243 mg kg−1 respectively. Mg/Al LDH-zeolite consistently demonstrated higher efficiency in reducing the bioavailability and translocation of heavy metals in maize tissues, confirming its potential as an effective adsorbent for soil remediation. Key mechanisms, including adsorption, surface complexation, ion exchange, precipitation, and structural incorporation, reduce metal mobility and bioavailability.

Efficiency of heat-treated sepiolite in the adsorption of Cd, Zn, and Co from aqueous solutions: A low-cost approach for wastewater treatment

This study investigated the adsorption of Cd, Co, and Zn ions onto unmodified and heat-treated sepiolite, focusing on the effect of contact time, initial pH, and heat pretreatments. Kinetic experiments were conducted in triplicate, and equilibrium experiments indicated that Co2+ had the highest adsorption preference, followed by Zn2+ and Cd2+. The adsorption efficiency for Co2+ significantly increased with higher initial pH, whereas Zn2+ and Cd2+ showed optimal adsorption at lower pH levels. Heat-treated sepiolite at 250 ℃ exhibited a higher surface area and adsorption capacity in comparison with unmodified and 150 ℃-treated sepiolite, which indicated the importance of heat pretreatment. The pseudo-second-order kinetic model better described the adsorption process, and it was confirmed chemisorption as the rate-limiting step. By increasing the contact time, adsorption rates enhanced, with equilibrium achieved within 480 min for all systems. Higher initial solute concentrations led to an increase in adsorption processes, with Co ions consistently showing higher adsorption efficiency in competitive multi-ionic solutions. Adsorption percentages varied with pH and thermal treatment, indicating the importance of these parameters in optimizing sepiolite’s adsorption capacity for heavy metal removal.

Preparation of Mesoporous Analcime/Sodalite Composite from Natural Jordanian Kaolin

In this work, a meso-macroporous analcime/sodalite zeolite composite was produced by a hybrid synthesis process between a complex template method and hydrothermal treatment at 220 °C of naturally abundant kaolinitic-rich clay, using dodecyltrimethylammonium bromide as an organic soft template to enhance the mesoporous structure. The chemical and morphological properties of the developed zeolites composite were characterized using powder X-ray diffraction (PXRD), attenuated total Reflectance–Fourier transform infrared spectroscopy (ATR-FTIR), thermogravimetric analysis (TGA), N2 adsorption/desorption; and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) methods were used to study the morphology, chemical composition and structure of the product. Two types of zeolite particles were obtained:(1) hollow microsphere with an attached analcime icositetrahedron of 30–40 µm in size and (2) sodalite microsphere with a ball-like morphology of 3–4 µm in size. Both N2 adsorption/desorption and surface area data confirmed the high potentiality of the produced zeolite composite to act as an excellent adsorbent to remove inorganic pollutants such as Cu, Cd, Cr, Ni, Zn, and Pb ions, organic pollutants such as dyes, phenolic compounds, and surfactants from water; and their high catalytic activity, especially in the oxidation reaction of volatile organic compounds. The catalytic activity and adsorption ability of the produced analcime/sodalite composite will be tested experimentally in future work.