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[Display omitted] Development of polymeric magnetic adsorbents is a promising approach to obtain efficient treatment of contaminated water. However, the synthesis of magnetic composites involving multiple components frequently involves tedious preparation steps. In the present study, a magnetic chitosan-palygorskite (MCP) nanocomposite was prepared through a straight-forward one pot synthesis approach to evaluate its lead (Pb2+) removal capacity from aqueous solution. The nano-architectural and physicochemical properties of the newly-developed MCP composite were described via micro- and nano-morphological analyses, and crystallinity, surface porosity and magnetic susceptibility measurements. The MCP nanocomposite was capable to remove up to 58.5 mg Pb2+ g−1 of MCP from water with a good agreement of experimental data to the Langmuir isotherm model (R2 = 0.98). The Pb2+ adsorption process on MCP was a multistep diffusion-controlled phenomenon evidenced by the well-fitting of kinetic adsorption data to the intra-particle diffusion model (R2 = 0.96). Thermodynamic analysis suggested that the adsorption process at low Pb2+ concentration was controlled by chemisorption, whereas that at high Pb2+ concentration was dominated by physical adsorption. X-ray photoelectron and Fourier transform infrared spectroscopy results suggested that the Pb adsorption on MCP was governed by surface complexation and chemical reduction mechanisms. During regeneration, the MCP retained 82% Pb2+ adsorption capacity following four adsorption–desorption cycles with ease to recover the adsorbent using its strong magnetic property. These findings highlight the enhanced structural properties of the easily-prepared nanocomposite which holds outstanding potential to be used as an inexpensive and green adsorbent for remediating Pb2+ contaminated water. [ABSTRACT FROM AUTHOR]

For human health and environment safety, it is of great significance to develop novel materials with high effectiveness for removal of lead from not only aqueous solutions but also human body and traditional Chinese medicines. Here, functional kiwi peel composite, manganese dioxide decorated kiwi peel powder (MKPP), is proposed for the removal of Pb2+ effectively. The adsorption of Pb2+ in aqueous solution is a highly selective and endothermic process and kinetically follows a pseudo-second-order model, which can reach equilibrium with the capacity of 192.7 mg/g within 10 min. Comprehensive factors of hydration energy, charge-to-radius ratio and softness of Pb2+ make a stronger affinity between MKPP and Pb2+. The possible adsorption mechanism involves covalent bond, electrostatic force and chelation, etc. MKPP can be efficiently regenerated and reused with high adsorption efficiency after five cycles. Besides, MKPP can remove over 97% of Pb2+ from real water samples. MKPP can also alleviate lead poisoning to a certain extent and make the Pb level of TCM extract meet the safety standard. This work highlights that MKPP is a promising adsorbent for the removal of Pb2+ and provides an efficient strategy for reusing kiwi peel as well as dealing with the problem of Pb pollution. • Novel manganese dioxide decorated kiwi peel powder was fabricated. • Interactions for adsorption involved covalent bond, electrostatic force and chelation. • Functional adsorbent showed a satisfactory lead adsorption performance. [ABSTRACT FROM AUTHOR]

In this study, crayfish shell was pyrolyzed at 600 °C to obtain a calcium-rich biochar (CS600). The biochar was saturated with Pb2+ in batch adsorption experiment. Six desorption reagents including HCl, HNO 3 , H 2 SO 4 , NaOH, EDTA and EDTA-2NaCa were then used to desorb Pb2+ from the post-adsorption CS600 to determine the desorption mechanism. Lead adsorption experiments were performed to determine the adsorption capacity of the regenerated CS600. HCl, HNO 3 , EDTA and EDTA-2NaCa presented good desorption effect with desorption rates all over 80%. Most of the regenerated biochars lost their lead adsorption ability due to the destruction of CaCO 3 mineral on their surface. Only the one desorbed by EDTA-2NaCa retained a preferable lead adsorption capacity. EDTA-2NaCa thus is a promising desorption reagent of CS600 for the removal of lead from aqueous solutions. [ABSTRACT FROM AUTHOR]

Biochar derived from soybean straw with AAEMs (alkali and alkaline earth metals) enrichment could efficiently remove heavy metals from contaminated water. In this study, the influences of pyrolysis temperature on the physicochemical property and adsorption performance of soybean straw biochar were investigated. The contributions of different adsorption mechanisms were analyzed quantitatively. The results show that the soybean straw biochar exhibits excellent Pb2+ adsorption performance (157.2–227.2 mg g−1), with an order of BC800 > BC400 > BC600 > BC700 > BC500. The mechanisms of metal ion exchange (37.49%–72.58%) and precipitation with minerals (22.38%–58.03%) mainly control the Pb2+ adsorption, whereas complexation with organic functional groups (OFGs) and cation-Cπ interaction make the less contribution. The order of cation exchange capacity (CEC) is BC400 > BC800 > BC700 > BC600 > BC500, showing a high correlation (0.965) with the contribution of metal ion exchange with AAEMs. Moreover, Ca exhibits the strongest exchange capacity. The contribution of precipitation is consistent with the variation of soluble CO 3 2− content in biochar. These results suggest that soybean straw biochar rich in AAEMs is a prospective adsorbent for Pb2+ elimination. [Display omitted] • Soybean straw biochar rich in AAEMs exhibits excellent Pb2+ adsorption performance. • The adsorption behavior is significantly affected by the pyrolysis temperature. • Metal ion exchange and precipitation with minerals dominate the Pb2+ adsorption. • The CEC and soluble CO 3 2− are key properties governing the adsorption capacity. [ABSTRACT FROM AUTHOR]

For fabricating a membrane with hydrophilic and complexing agent groups, a new dithiocarbamate-based polymer (DTCP) containing dithiocarbamate, thioamide, and ethereal oxygen groups was synthesized and blended in polysulfone (PSF) matrix with 1, 2, 5, and 10 wt% proportion. The membranes were produced by the nonsolvent induced phase separation method. For DTCP characterization, NMR, FTIR, TGA and GPC techniques were used. SEM images show that no morphological change can be seen even in 10 wt% blended membranes. AFM surface images show that the roughness of 5 and 10 wt% membranes extremely increased. The performance of the DTCP/PSF membranes were investigated in the separation of lead ions and Reactive Yellow 39 dye from the contaminated water. The outcomes indicated that by increasing the amount of DTCP up to 10 wt%, the pure water flux, bovine serum albumin flux, and the lead removal increased very efficiently compared to the bare one. Blending of more than 1 wt% DTCP, cause to removal of 99.6% lead ions. The water contact angle decreased by the adding of DTCP, caused to increase fouling resistance. The results of this research shows that the synthesized DTCP can be used as a good additive for improving membrane permeability, anti-fouling and especially heavy metal removal efficiency. • Dithiocarbamate-based polymer (DTCP) were synthesized as a hydrophilic additive. • DTCP was used as complexing agent to improve lead removal efficiency of membrane. • 2 wt% DTCP/PSF membrane showed 99.6% Pb(II) removal with 161 L/m2h.bar permeability. • DTCP enhanced membrane hydrophilicity and antifouling properties. [ABSTRACT FROM AUTHOR]

Hydrochar produced via hydrothermal carbonization of grape pomace was considered as novel sorbent of Pb 2+ from aqueous solution. In order to enhance the adsorption capacity, hydrochar was chemically modified using 2 M KOH solution. Both materials were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray diffraction technique. Batch experiments were performed to examine the effect of sorbent dosage, pH and contact time. Obtained results showed that the KOH treatment increased the sorption capacity of hydrochar from 27.8 mg g −1 up to 137 mg g −1 at pH 5. Adsorption of lead on either of the materials was achieved through ion-exchange mechanism, chemisorption and Pb 2+ -π interaction. The Sips isotherm model gave the best fit with the experimental data obtained for Pb 2+ sorption using activated hydrochar. The adsorption kinetic followed a pseudo second-order model. Thermodynamic parameters implied that the Pb 2+ binding for hydrochar surface was spontaneous and exothermic process. Findings from this work suggest that the hydrothermal carbonization is a promising route for production of efficient Pb 2+ sorbents for wastewater treatment. [ABSTRACT FROM AUTHOR]

In this study, an adsorbent made of alginate (Alg) caged magnesium sulfide nanoparticles (MgS) microbeads were used to treat lead ions (Pb2+ ions). The MgS nanoparticles were synthesized at low temperatures, and Alg@MgS hydrogel microbeads were made by the ion exchange process of the composite materials. The newly fabricated Alg@MgS was characterized by XRD, SEM, and FT-IR. The adsorption conditions were optimized for the maximum removal of Pb2+ ions by adjusting several physicochemical parameters, including pH, initial concentration of lead ions, Alg/MgS dosage, reaction temperature, equilibration time, and the presence of co-ions. This is accomplished by removing the maximum amount of Pb2+ ions. Moreover, the adsorbent utilized more than six times with a substantial amount (not less than 60%) of Pb2+ ions was eliminated. Considering the ability of sodium alginate (SA) for excellent metal chelation and controlled nanosized pore structure, the adsorption equilibrium of Alg@MgS can be reached in 60 min, and the highest adsorption capacity for Pb2+ was 84.7 mg/g. The sorption mechanism was explored by employing several isotherms. It was found that the Freundlich model fits the adsorption process quite accurately. The pseudo-second-order model adequately described the adsorption kinetics. [ABSTRACT FROM AUTHOR]

The current study presents a viable and straightforward method for synthesizing titanium lanthanum three oxide nanoparticles (TiLa) and their decoration onto the ferrous graphene oxide sheets to produce FeGO-TiLa as efficient magnetic adsorbent. Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and vibration sample magnetometer (VSM) were used to evaluate the physical and chemical properties of the produced nanocomposites. The FeGO-TiLa was used to enhance the removal of lead ions from aqueous solution. The FeGO-TiLa nanocomposite exhibited a much higher removal efficiency (93%) for lead ions than pure TiLa nanoparticles (81%) and magnetic graphene oxide (74%). The influence of FeGO-TiLa dosage, contact time, solution pH, solution temperature, and starting quantity on the lead ions was evaluated and adjusted. The investigations demonstrated that a pH 6 with 40 mg adsorbent resulted in >91% removal of lead ions at ambient temperature after 120 min. Isotherm models were used to analyze experimental results, and Langmuir model fitted the data well as compared Freundlich model with a maximum adsorption capacity of 109.89 mg g−1. Kinetic and studies are performed the lead adsorption over FeGO-TiLa follow pseudo-second-order rate. Langmuir and Free energy suggested the lead ions uptake with FeGO-TiLa was monolayer and physical adsorption mechnaism, respectively. Finally, the FeGO-TiLa nanocompoiste can be used as an alternative adsorbent for water remediation. [Display omitted] • Novel titanium lanthanum oxide nanoparticles doped iron graphene oxide was used. • The FeGO-TiLa as magnetic adsorbent was used to enhance the removal of lead from water. • The FeGO-TiLa had a higher removal (93%) for lead than pure LaTiO3 (81%). • Langmuir suggested the lead ions uptake with FeGO-TiLa was a monolayer. [ABSTRACT FROM AUTHOR]

Population explosion, depletion of water resources and prolonged droughts and floods due to climatic change lead to scarcity of pure and hygienic drinking water in most of the developing countries. Recently nanomaterials attained considerable attention as biosorbent for water purification purpose. However difficulties in removing polymeric surfactants and organic solvents used for nanoproduction and instability of the generated nanoparticles limit the scope of this approach in water cleanup. Here, we describe a novel green method for synthesizing polysaccharide nanoparticles in aqueous medium using honey as the capping agent. The highly stable alginate nanoparticles, characterized by various microscopic and spectroscopic techniques, exhibited a maximum uptake capacity of 333 mg g −1 of Pb(II) ions from aqueous solution. The effect of various parameters such as initial metal concentration, pH, contact time, temperature and adsorbent dose on sorption process was investigated in batch mode technique. The maximum removal percentage was 94.81 at 45 °C and at pH 4.5 in 60 min contact time. The biosorption followed Freundlich model indicating multilayer adsorption and pseudo second order kinetics. The mechanism involves both surface adsorption and pore diffusion. The positive values of ΔH°, ∆S° and the negative value of ΔG°, confirmed the endothermic nature, randomness and spontaneity of biosorption process. [ABSTRACT FROM AUTHOR]

In this study, lead removal from aqueous solutions using biochar derived from olive mill solid and liquid wastes has been investigated by applying batch experiments and geochemical modelling. The batch adsorption experiments included the assessment of several key parameters such as the contact time (kinetic), initial concentration (isotherm), pH, adsorbent dose, and the presence of competitive cations, whilst the geochemical modelling focused on the involved adsorption mechanisms using the PHREEQC code. The kinetic studies showed that lead adsorption is a relatively fast process, where intraparticle diffusion is the rate-limiting step. Biochar dose, solution pH and the presence of competitive ions significantly affected the Pb adsorption effectiveness by the biochar. Especially the higher Pb removal percentages were observed in mono-elemental solutions with high biochar dose at mildly acidic solution pH values. The maximum Pb adsorption capacity of biochar was estimated as 40.8 mg g−1 which is higher than various biochars derived from sludge, lignocellulosic and animal biomasses. On the other hand, the geochemical modelling employing the PHREEQC code showed that ion exchange and Pb precipitation are the main reactions controlling its removal from aqueous solutions, whilst surface complexation is insignificant, mainly due to the low surface functional groups on the used biochar. • Utilise olive mill solid waste (OMSW) biochar to remove Pb from aqueous solutions. • Batch sorption experiments described by Elovich kinetic equation and Sips isotherm model. • Modelling sorption process using the PHREEQC code. • Ion-exchange and precipitation were found as the key retention mechanisms of Pb. • OMSW biochar can be applied as a cost-effective and environmentally friendly sorbent. [ABSTRACT FROM AUTHOR]

Abstract: Titanium phosphate (TiP) exhibits preferable sorption toward lead ion in the presence of competing calcium ions at high levels, however, it is present as fine or ultrafine particles and cannot be directly employed in fixed-bed or any flow-through systems due to the excessive pressure drop and poor mechanical strength. In the present study a new hybrid sorbent TiP-001 was fabricated by impregnating titanium phosphate (TiP) nanoparticles onto a strongly acidic cation exchanger D-001 for enhanced lead removal from waters. D-001 was selected as a host material mainly because of the Donnan membrane effect resulting from the immobilized sulfonic acid groups bound on the exchanger matrix, which would enhance permeation of the target metal cation prior to effective sequestration. TiP-001 was characterized by transmission electron micrograph (TEM), X-ray diffraction (XRD), and pH-titration. Batch and column sorption onto TiP-001 was assayed to evaluate its performance as compared to the host exchanger D-001. Lead sorption onto TiP-001 is a pH-dependent process due to the ion-exchange nature, and its sorption kinetics follows the pseudo-second-order model well. Compared to D-001, TiP-001 displays highly selective lead sorption in the presence of competing calcium cations at concentration of several orders higher than the target metal. Fixed-bed sorption of a synthetic feeding solution indicates that lead retention by TiP-001 results in a conspicuous decrease of this toxic metal from 0.50 to below 0.010 mg/L (drinking water standard recommended by WHO). Moreover, its feasible regeneration by dilute HCl solution also favors TiP-001 to be a feasible sorbent for enhanced lead removal from water. [Copyright &y& Elsevier]

Abstract: Spherical silica and zirconia mixed titania and pure titania samples were prepared in presence of cetyltrimethylammonium bromide (CTAB) through controlled hydrolysis of corresponding metal alcoxides. Effect of surfactant amount and calcinations temperature on morphology, surface area and photocatalytic activity is studied using PXRD, SEM, FTIR, Solid state UV–vis spectroscopy and BET surface area. It is well observed that in presence of 2 mol% CTAB, uniform sized spherical oxide particles can be synthesized. However, increasing or decreasing the surfactant amount does not favor the spherical particle formation. Material synthesis in presence of CTAB not only helps in the spherical particle formation but also increases the surface area and visible light absorption. Studies on photocatalytic lead removal with respect to calcination temperature indicate that the calcination at 500 °C is most suitable for the best photocatalytic activity. Mixing of zirconia and silica helps in anatase phase stabilization even at 900 °C calcination. Accordingly low decrease in surface area even at 900 °C calcination is observed. Due to the phase stabilization and higher surface area binary oxide materials showed comparatively better photocatalytic activity even after calcination at 900 °C. So it can be concluded that present synthesis approach can produce uniform sized spherical binary oxide materials with better photocatalytic activity in visible light. [Copyright &y& Elsevier]

Heavy metal ions in aqueous solutions are taken into account as one of the most harmful environmental issues that ominously affect human health. Pb(II) is a common pollutant among heavy metals found in industrial wastewater, and various methods were developed to remove the Pb(II). The adsorption method was more efficient, cheap, and eco-friendly to remove the Pb(II) from aqueous solutions. The removal efficiency depends on the process parameters (initial concentration, the adsorbent dosage of T-Fe3O4 nanocomposites, residence time, and adsorbent pH). The relationship between the process parameters and output is non-linear and complex. The purpose of the present study is to develop an artificial neural networks (ANN) model to estimate and analyze the relationship between Pb(II) removal and adsorption process parameters. The model was trained with the backpropagation algorithm. The model was validated with the unseen datasets. The correlation coefficient adj.R2 values for total datasets is 0.991. The relationship between the parameters and Pb(II) removal was analyzed by sensitivity analysis and creating a virtual adsorption process. The study determined that the ANN modeling was a reliable tool for predicting and optimizing adsorption process parameters for maximum lead removal from aqueous solutions. • ANN model developed for Pb(II) removal from aqueous solutions. • Optimum process window was identified for Pb(II) removal. • Quantitative estimation between adsorption and Pb(II) was established. • A user-friendly standalone ANN model developed to analyze the adsorption process. [ABSTRACT FROM AUTHOR]

Polyacrylic acid capped Fe 3 O 4 – Cu-MOF (i-MOF) hybrid was prepared for rapid and selective lead removal, with 93% removal efficiency, exceptional selectivity, and adsorption capacity of 610 mg/g and 91% of i-MOF hybrid could be easily separated from the contaminated water using magnetic separation. The adsorption process followed a pseudo-second-order model and the adsorption efficiency decreased from 93% to 83% on raising the temperature from 25 °C to 40 °C. The change in equilibrium adsorption capacity with respect to equilibrium adsorbate concentration followed the Langmuir isotherm model. i-MOF had a high selectivity coefficient and removal efficiency for lead ions even when exposed simultaneously with naturally abundant cations (Na(I), Ca(II), Mg(II)). Release of Cu(II) ions from the i-MOF after Pb(II) removal suggested suggested ion-exchange to be the dominant removal mechanism. This new finding for Pb(II) removal with excellent adsorption performance using i-MOF through ion exchange based approach is a viable option for treating lead contaminated water. Image 1 • Successful synthesis of Fe 3 O 4 –Cu-MOF (i-MOF) hybrid. • i-MOF removed 93% Pb(II), with a removal capacity of 610 mg/g. • Ion exchange was the dominant Pb(II) removal mechanism. • Efficient recovery (91%) of i-MOF hybrid using magnetic separation. [ABSTRACT FROM AUTHOR]