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Biodegradable and eco-friendly composite adsorbent was synthesized from modified jute fiber and gelatin and evaluated its efficacy in removing cadmium (Cd2+), lead (Pb2+), and chromium (Cr3+) ions from an aqueous solution. The prepared sample was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and energy dispersive X-ray analyses, which revealed that gelatin successfully intercalated into the microcrystalline cellulose matrix. In batch adsorption studies, the effects of pH, adsorbent dosage, initial metal ions concentration, and temperature on the removal of heavy metal ions were investigated. The adsorption capacity of the composite varied with changing parameters, and the maximum removal efficiency obtained for Cd2+, Pb2+, and Cr3+ was 95%, 88%, and 70%, respectively, at pH 6 with 60 ppm of each metal ions concentration and an adsorbent dosage of 1.0 g L−1. Different functional groups in composite adsorbent facilitated heavy metal ions adsorption. Five error analysis methods were used to evaluate the fit the goodness of the data. The equilibrium adsorption and kinetic data were well-fitted with the Langmuir isotherm model and pseudo-second-order, respectively. Moreover, the thermodynamic study showed that the adsorption was spontaneous, chemisorption, and endothermic. Our work offers a sustainable and biodegradable composite synthesized from modified jute fiber and gelatin for multimetal ions removal from an aqueous, which is an eco-friendly alternative to conventional nonbiodegradable adsorbents with potential environmental risks. [ABSTRACT FROM AUTHOR]

Most galvanic process industries treat their effluents by chemical precipitation methods. Such a method produces an amount of galvanic sludge that is often disposed of inappropriately to the environment, causing major environmental damage. These rejects present high concentrations of toxic metallic ions, such as copper (Cu(II)), lead (Pb(II)), nickel (Ni(II)), and cadmium (Cd(II)). Several alternatives have been proposed to contribute in a cheaper and efficient way to treat these effluents. This study aimed to describe the results obtained in the removal of the concentrations of Cu(II), Ni(II), Cd(II), and Pb(II) ions, present in an aqueous solution, by the use of a hybrid system combining the adsorption and electroflotation processes simultaneously. The adsorbent materials used were two Brazilian soil clays classified as sodium clay (SC) and ferric clay (FC). For the electroflotation process, aluminum, iron, and stainless-steel electrodes were used. The obtained data showed good efficiency in the removal of the four metallic ion concentrations. The best results presented a reduction in the concentration of Cu(II), Ni(II), Cd(II), and Pb(II) ions of 50.11%, 36.71%, 21.59%, and 23.43%, respectively, when it was used the hybrid system formed by the ferrous clay as adsorbent and the aluminum electrode for the electroflotation process. [ABSTRACT FROM AUTHOR]

Removal of heavy metal ions such as cadmium, lead, chromium, and iron from industrial wastewater is one of the most critical environmental problems. In this research, natural and low-cost adsorbents like the tangerine peel, bovine gut, tea waste, and sunflower seed hull were used for adsorption of heavy metals, such as chromium and iron, from contaminated solutions. The effects of environmental factors such as contact time, pH, the amount of adsorbent dose, and the initial concentration of metal ions in synthetic solution were investigated to obtain optimal conditions for the adsorption of heavy metal ions. For separation of chromium metal ion from aqueous solution, tea waste, tangerine peel, bovine gut, and sunflower seeds hull showed adsorption capacity of 85%, 51%, 46%, and 34%, respectively, while for the adsorption of iron (III), the adsorption capacities of tea waste, bovine gut, tangerine peel, and sunflower seeds hull were 96%, 96%, and 87%, respectively. The adsorption isotherms were in decent correlation with the Langmuir and Freundlich isotherm models. The adsorption kinetics of iron and chromium has a proper validation with the pseudo-second-order kinetic model. The BET and FTIR analyses were also reported to investigate the adsorption properties. This study suggests these adsorbents as low-cost and economical materials for the adsorption of chromium and iron ions with a high adsorption rate. [ABSTRACT FROM AUTHOR]

The aim of this study is the valorization of the Moroccan clays (QC-MC and QC-MT) from the Middle Atlas region as adsorbents for the treatment of water contaminated by cadmium Cd (II) ions. The physicochemical properties of natural clays are characterized by ICP-MS, XRD, FTIR, and SEM techniques. The adsorption process is investigated as a function of adsorbent mass, solution pH, contact time, temperature, and initial Cd (II) ion concentration. The kinetic investigation shows that the adsorption equilibrium of Cd (II) ions by both natural clays is reached after 30 min for QC-MT and 45 min for QC-MC and fits well to a pseudo-second-order kinetic model. The isotherm study is best fitted by a Freundlich model, with the maximum adsorption capacity determined by the linear form of the Freundlich isotherm being 4.23 mg/g for QC-MC and 5.85 mg/g for QC-MT at 25°C. The cadmium adsorption process was thermodynamically spontaneous and exothermic. The regeneration process showed that these natural clays had excellent recycling capacity. Characterization of the Moroccan natural clays before and after the adsorption process through FTIR, SEM, XRD, and EDX techniques confirmed the Cd (II) ion adsorption on the surfaces of both natural clay adsorbents. Overall, the high adsorption capacity of both natural clays for Cd (II) ions removal compared to other adsorbents motioned in the literature indicated that these two natural adsorbents are excellent candidates for heavy metal removal from aqueous environments. [ABSTRACT FROM AUTHOR]

Herein, we prepared the L-histidine- (His-) protected silver nanoclusters (Ag NCs) by the microwave synthesis method. The synthesis process was rapid, facile, and environmentally friendly. Under 356 nm excitation, the as-prepared Ag NCs exhibited the blue fluorescence, and the fluorescence emission peak was located at 440 nm. The Ag NCs could successfully detect trace copper (Cu2+) ions in the aqueous solution and the limit of detection (LOD) was as low as 0.6 pM. Interestingly, the Ag NCs showed a different pH-dependent selectivity for both Cu2+ and iron (Fe3+) ions with no responses to other heavy metal ions. Furthermore, the as-fabricated fluorescent sensing system was utilized to detect glutathione (GSH, the LOD was 0.8 nM) by using the "switch-on" fluorescence recovery of Ag NCs through adding glutathione (GSH) to the Cu2+-Ag NCs solution. [ABSTRACT FROM AUTHOR]

This paper presents studying the performance of three types of polyethersulfone (PES) membrane for the simultaneous removal of Co2+ ions, Cd2+ ions, and Pb2+ ions from binary and ternary aqueous solutions. Co2+ ions, Cd2+ ions, and Pb2+ ions with two different initial concentrations (e.g., 10 and 50 ppm) were selected as examples of heavy metals that contaminate the groundwater as a result of geological and human activities. This study investigated the effect of types of PES membrane and metal ions concentration on the separation process. For the binary aqueous solutions, the permeation flux of the PES2 membranes was higher for the separation process of solutions containing 50 ppm of Cd2+ ions and 10 ppm of Co2+ ions (24.7 L/m2·h) and Pb2+ ions (23.7 L/m2·h). All the metals in the binary solutions had high rejection when their initial concentration was lower than the initial concentration of the other metal present in the same solution. Using PES2, the maximum rejection of Cd2+ ions was 61.3% when the initial concentrations were 50 ppm Pb2+ ions: 10 ppm Cd2+ ions and 55.4% for Pb2+ ions when the initial concentrations were 10 ppm Pb2+ ions: 50 ppm Cd2+ ions. For the ternary aqueous solutions, the rejection and the permeation flux of the PES membranes increased with decreasing the heavy metal initial concentration. Using PES2, the maximum permeation flux was 21.6 L/m2·h when the initial concentration of the metals was 10 ppm; and the maximum rejection of the metals obtained at initial concentration of 10 ppm was 50.5% for Co2+ ions, 48.3% for Cd2+ ions, and 40% for Pb2+ ions. The results of the filtration process using PES2 of simulated contaminated-groundwater indicated the efficient treatment of groundwater containing Co2+, Cd2+, and Pb2+ ions. [ABSTRACT FROM AUTHOR]

Herein, by using the green and cheap L-cysteine as the precursor, nitrogen and sulfur codoped carbon dots (NS-CDs) were synthesized via a facile one-step hydrothermal method. The obtained NS-CDs showed the relatively narrow size distributions (2.1~3.9 nm) with the lattice spacing of 0.29 nm, as well as the excitation-dependent photoluminescence (PL) emission activity with the quantum yield (QY) of 18%. More interestingly, the PL intensity of NS-CDs was quenched by the addition of copper or lead ions (Cu2+ or Pb2+), which was shown in the tradition detection method by PL spectra. The NS-CDs exhibited ultrasensitive colorimetric sensing capability for both Cu2+ and Pb2+ by the color variance using naked eyes without any further treating. Two different coupling ways for detecting Pb2+ and Cu2+ were induced by the analysis of the Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). And the as-prepared NS-CDs showed their potential application in the heavy metal ions detection for the wastewater determination. [ABSTRACT FROM AUTHOR]

A more applicable adsorbent was fabricated using industrial wastes such as red mud, fly ash, and riverbed sediments. The heavy metal inside the raw materials created metal hydroxy on the adsorbent surface that offered elevated adsorption capacity for phosphorus. The required equilibrium time for the adsorption is only 10 min. The theoretical maximum adsorption capacity of the adsorbent was 9.84 mg·g−1 inferred from the Langmuir adsorption isotherm. Higher solution pH favored phosphorus adsorption. Kinetics study showed that the adsorption could be better fitted by the pseudo-second-order kinetic model. The presence of coexisting anions had no significant adverse impact on phosphorus removal. The speciation of the adsorbed phosphorus indicated that the adsorption to iron and aluminum is the dominating adsorption mechanism. Moreover, a dynamic adsorption column experiment showed that, under a hydraulic time of 10 min, more than 80% of the phosphorus in the influent was removed and the surplus phosphorus concentration was close to 0.1 mg L−1. The water quality after adsorption revealed its applicability in real treatment. Consequently, the adsorbent synthesized from industrial wastes is efficient and applicable due to the high efficiency of phosphorus removal and eco-friendly behavior in solutions. [ABSTRACT FROM AUTHOR]

Cola-nut leaf is an agricultural waste which was used in this research as biosorbent for the adsorption of Cd2+and Cr6+ from aqueous solutions. The leaves of cola nut were modified using 0.1 M HCl. Modified cola nut leaves biosorbent showed slightly higher percentage sorption than the unmodified leaves, for both heavy metals with increasing contact time, having greater affinity for Cd2+. The equilibrium sorption data was attained using the batch technique with increased pH (9) and increased adsorbent dose (1 g/25 cm3 of adsorbate) and initial metal concentration. The functional group of cola nut leaves before and after adsorption was determined using Fourier Transform Infrared Spectroscopy (FTIR). Kinetics data were best fitted to a pseudo-second-order model. Equilibrium data were better described by the Temkin isotherm model with a multilayer adsorption capacity. The study showed that leaves of cola nut are a promising biosorbent for Cd2+ and Cr6+ which could be utilized for industrial wastewater remediation. [ABSTRACT FROM AUTHOR]

This paper presents the characteristics of fly ash which was modified by 2-mercaptobenzothiazole (MBT) and sodium dodecyl sulfate (SDS) as the surfactants after treating with 1M NaOH solution. The change in morphology, specific surface area, crystal structure, and composition of the unmodified and modified fly ash was evaluated by FTIR, XRD, FESEM, BET, and EDX methods and techniques. The FTIR spectra of modified fly ash showed that there was no chemical reaction between the surfactants and fly ash. The XRD patterns and FESEM images indicated that modified fly ash had zeolite structure with a pore size of about 50 nm. Heavy metal ion adsorption behavior as well as adsorption isotherm models (Langmuir and Freundlich) of Cd2+ and Hg2+ ions of the unmodified and modified fly ash were also investigated and discussed. The amount of adsorbed ions of the modified fly ash was higher than that of the unmodified fly ash. The calculated results from the adsorption data according to the adsorption isotherm models of the above ions displayed that the Langmuir isotherm model was complied for the Cd2+ adsorption process while the Freundlich isotherm model was fitted for the Hg2+ adsorption process. [ABSTRACT FROM AUTHOR]

Egyptian oil shale was investigated as a source of adsorbent for removal of zinc from aqueous solutions. Egyptian oil shale (OS) was used as an adsorbent without any treatment, then thermally activated in absence of air (Carbo-OS), and separately burned to produce ash (OS-ash). Egyptian oil shale was also chemically activated by zinc chloride (ZnCl2-OS) respectively. The present study aims at investigating the removal of Zn2+ ions from an aqueous solution via adsorption and thermal and chemical activation of locally sourced oil shale. Also, the effect of different operation parameters, like heavy metal and sorbent concentration as well as adsorbent's uptake time of heavy metals is studied. It was found that activated oil shale successfully removed high amount of Zn from an aqueous solution. As the adsorbent concentration was increased keeping zinc concentration constant, greater metal removal from the solution was observed. And, as the zinc concentration was increased keeping sorbent concentration constant, higher metal loading per unit weight of the sorbent was achieved. The Langmuir isotherm model fit the experimental data of Zn2+ ions. The results indicated that oil shale could be used to adsorb Zn2+ ions and that thermally activated oil shale resulted in 99% removal for Zn2+. [ABSTRACT FROM AUTHOR]

Treatment of wastewater is becoming a concern of an increasing prominence. Trace amounts of toxic metalloids and heavy metals (HMs) would contaminate large volumes of water. Being present as traces, removal of these ultratrace contaminants from wastewater is challenging. Adsorption of HMs onto raw (RPP) and burnt (BPP) potato peels (PP) is presented in the current treatise. Both adsorbents (RPP and BPP) proved to be efficient in removing Cd(II), Co(II), Cu(II), Fe(II), La(III), Ni(II), and Pb(II) from aqueous solutions. BPP was a more efficient adsorbent compared to RPP. Ecodesign of a model, green adsorbent was structured executing a multivariate approach, design of experiments (DoE). The purpose of using DoE is to maximize the efficiency of BPP (carbonaceous biomass) as a versatile adsorbent. Plackett–Burman design (PBD) was used as a screening phase. Four factors were considered: pH, contact time (CT), heavy metal concentration (HMC), and the adsorbent dose (AD). The Pareto chart of standardized effects shows that the most influential factor is the HMC. These data were confirmed by analysis of variance (ANOVA). Derringer's function was operated to find the best factorial blend that maximizes the adsorption process. The percentage (%) removal of Cd(II), for example, was maximized hitting 100%. Adsorbent surface characterization was performed using FTIR, BET, SEM, TGA/dTG, and EDX analyses. Adsorption was found to be physisorption that follows Temkin isotherm with sorption energy 66 kJ/mole. Adsorption kinetics was found to be pseudo-first-order. Adsorption capacity (qm) for BPP was 239.64 mg/g. The diffusion inside the particles was very limited, while the initial rate of the adsorption was extremely high as shown by the Elovich plot. [ABSTRACT FROM AUTHOR]

The capacities of the p-t-butylcalix[8]arene (abbreviated as H8L) host to extract toxic divalent heavy metal ions and silver from aqueous solution phases containing ammonia or ethylene diamine to an organic phase (nitrobenzene, dichloromethane, or chloroform) were carried out. When the metal ions were extracted from an aqueous ammonia solution, the metal ion selectivity for extraction was found to decrease in the order Cd2+> Ni2+> Cu2+> Ag+> Co2+> Zn2+. When the aqueous phase contained ethylene diamine, excellent extraction efficiencies of 97% and 90% were observed for the heavy metal ions Cu2+ and Cd2+, respectively. Under the same conditions the extraction of octahedral type metal ions, namely, Co2+ and Ni2+, was suppressed. The extraction of transition metal cations by H8L in ammonia and/or amine was found to be pH dependent. Detailed analysis of extraction behavior was investigated by slope analysis, the continuous variation method, and by loading tests. [ABSTRACT FROM AUTHOR]

The present study focuses on the response surface methodology (RSM) for the optimization of lead removal from an aqueous solution by a novel superparamagnetic nanocomposite. A rotatable central composite design and the response surface methodology were used to conduct and to analyze the experiments, respectively. The adsorption process was investigated as a function of the four factors consisting of pH (4.0-6.0), temperature (20°C-60°C), initial lead concentration (10-90 mg/L) and adsorbent dosage (0.2-1.0 g/L). The maximum lead adsorption capacity was obtained to be 124.955 mg/g under the optimal conditions of 5.49, 60°C, 89.08 mg/L, and 0.48 g/L for the solution pH, temperature, initial lead ion concentration, and the adsorbent dosage, respectively. The desirability function was used to find an optimum point where the desired conditions could be obtained. The superparamagnetic nanocomposite could be used as an adsorbent for the removal of toxic heavy metals from water and wastewater. [ABSTRACT FROM AUTHOR]

This paper evaluates the pyrolysis conditions applied during the synthesis of bovine bone char and the effect of these parameters in its adsorption properties for heavy metal removal from aqueous solution at batch reactors. The synthesis route has been analyzed in detail and the surface interactions involved in the adsorption process has been studied and discussed using different characterization techniques, given a special emphasis on X-ray photoelectron spectroscopy (XPS) analysis. A proper selection of the pyrolysis conditions improved the metal uptake of bone chars by 143% where the adsorption capacities ranged from 68.3 up to 119.4 mg/g. The removal performance followed the trend Cd2+ > Zn2+ > Ni2+. However, the multicomponent removal of Zn2+, Cd2+, and Ni2+ ions in both binary and ternary mixtures was a strong antagonistic adsorption process. XPS analysis confirmed that the ion exchange between the calcium, from the hydroxyapatite structure of bone char, and the heavy metals in solution played an important role in the adsorption process. These findings are useful to enhance the efficacy of heavy metal removal from aqueous solution using bone char. [ABSTRACT FROM AUTHOR]

Here we report the sensing properties of the aqueous solution of meso-tetra(N-methyl-4-pyridyl)porphine tetrachloride (1) for simultaneous detection of toxic metal ions by using UV-vis spectroscopy. Cationic porphyrin 1 displayed different electronic absorptions in UV-vis region upon interacting with Hg2+, Pb2+, Cd2+, and Cu2+ ions in neutral water solution at room temperature. Quite interestingly, the porphyrin 1 showed that it can function as a single optical chemical sensor and/or metal ion receptor capable of detecting two or more toxic metal ions, particularly Hg2+, Pb2+, and Cd2+ ions coexisting in a water sample. Porphyrin 1 in an aqueous solution provides a unique UV-vis sensing system for the determination of Cd2+ in the presence of larger metal ions such as Hg2+, or Pb2+. Finally, the examination of the sensing properties of 1 demonstrated that it can operate as a Cu2+ ion selective sensor via metal displacement from the 1-Hg2+, 1-Pb2+, and 1-Cd2+. [ABSTRACT FROM AUTHOR]

This paper describes the effect of surface nanomodification of porous adsorbents. Two commercial activated carbons (ACs), AG-5 and NWC coconut shell based, were used as adsorbents. The adsorbents were modified with carbon nanotubes (CNTs) by chemical vapour deposition. The CNTs were synthesized in the presence of a metal-oxide catalyst prepared using a citrate solgel method. The concentration of metal ions was evaluated by a spectrophotometric method. Experimental results show that the nanomodification of ACs increased their equilibrium adsorption of heavy metals (Ni2+ and Co2+) by 10-30%. Besides, the adsorption behaviour of these metal ions on the standard and nanomodified ACs was determined based on adsorption isotherms. A theoretical description of the adsorption mechanism is presented, and equilibrium constants were calculated. Experimental data on the adsorption of the heavy-metal ions on the nanomodified carbons were successfully fitted to the Langmuir and Freundlich models. [ABSTRACT FROM AUTHOR]

The use of waste biomaterial for the adsorption of heavy metal ions is an economically appealing alternative to conventional metal ion removal methods. In the present work, S. cerevisiae biomass has been shown to be capable of the simultaneous removal of more than 98% of Pb(II) ions, 60% of Zn(II) ions and up to 55% of Cu(II) ions from aqueous solutions in the 10-50 mg/l concentration range. Model equations describing the removal efficiency of each metal ion were determined using Response Surface Methodology (RSM) with respect to operating conditions such as pH, initial metal ion concentration and biomass dosage. Characterization of the metal ion-biomass interactions responsible for biosorption was studied employing zeta potential measurements, BET, FT-IR and EDX techniques; these indicated that the uptake of metal ions by non-living yeast was a surface adsorption phenomenon. The results proved the involvement of an ion-exchange mechanism between the adsorbing metal ions and the cell walls. In the presence of the complete range of metal ions studied, yeast cells were more selective towards Pb(II) ions. [ABSTRACT FROM AUTHOR]