Synthesis and characterization of chitosan Schiff base grafted with formaldehyde and aminoethanol: As an effective adsorbent for removal of Pb(II), Hg(II), and Cu(II) ions from aqueous media.

Grafted chitosan materials show the characteristics of high stability, easy separation and recovery, and good heavy metal adsorption capacity, and have received much attention in the adsorption process. Therefore, in this work, novel grafted chitosan-based adsorbent CS-EHBSB@F-AE was prepared by a one-pot reaction of chitosan (CS), 3-ethoxy-4-hydroxybenzaldehyde (EHB), formaldehyde (F) and aminoethanol (F). The microstructure and morphology of the as-prepared composite CS-EHBSB@F-AE were characterized by FT-IR, TGA, DSC, FE-SEM, and BET analyses. The adsorption performance of the as-prepared CS-EHBSB@F-AE composite on Pb(II), Hg(II), and Cu(II) ions from aqueous was investigated using batch experiment and the effects of the initial pH of the solution, contact time, and initial metal ions concentration and temperature on the adsorption efficiency were investigated and discussed. At the best conditions, CS-EHBSB@F-AE exhibited remarkable adsorption capacity of 246.7 mg/g, 203.9 mg/g, and 234.4 mg/g in absorbing Pb(II), Hg(II), and Cu(II), respectively. The adsorption equilibrium and the kinetic studies confirmed that the ions adsorption process fits well with the Langmuir isotherm and pseudo-second-order (PSO) models. Additionally, the adsorption efficiency of Pb(II), Hg(II), and Cu(II) metal ions by the composite CS-EHBSB@F-AE was reduced by increasing the temperature from 298 K to 318 K. In addition, after the sixth ads/des cycles, the as-prepared adsorbent still exhibited high removal efficiency with a decrease in adsorption efficiency of Pb(II) (5.53 %), Hg(II) (15.43 %) and Cu(II) (8.27 %). Finally, we proposed that the ions adsorption by CS-EHBSB@F-AE has happened using the coordination of active groups containing nitrogen and oxygen atoms on the surface of the adsorbent with the Pb(II), Hg(II), and Cu(II) metal ions.

Promoting microalgal biofilm formation by crushed oyster shell-hydroxyapatite layer on micropatterned aluminum coating for heavy metal ions removal.

Microalgal biomass has shown inspiring potential for the heavy metal removal from wastewater, and forming microalgal biofilm is one of the sustainable methods for the microalgal biomass production. Here we report the formation of microalgal biofilm by accelerated colonization of typical algae Chlorella on thermal sprayed aluminum (Al) coatings with biologically modified surfaces. Micro-patterning surface treatment of the Al coatings promotes the attachment of Chlorella from 6.31 % to 17.51 %. Further enhanced algae attachment is achieved through liquid flame spraying a bioactive crushed oyster shell-hydroxyapatite (CaCO3-HA) composite top layer on the micropatterned coating, reaching 46.03-49.62 % of Chlorella attachment ratio after soaking in Chlorella suspension for 5 days. The rapidly formed microalgal biofilm shows an adsorption ratio of 95.43 % and 85.23 % for low concentration Zn2+ and Cu2+ in artificial seawater respectively within 3 days. Quick interaction has been realized between heavy metal ions and the negatively-charged extracellular polymeric substances (EPS) matrix existing in the biofilm. Fourier transform infrared spectroscopy (FTIR) results indicate that both carboxyl and phosphoryl groups of biofilms are crucial in the adsorption of Cu2+ and the adsorption of Zn2+ is due to the hydroxyl and phosphate groups. Meanwhile, the biofilm could act as a barrier to protect Chlorella against the attack of the heavy metal ions with relatively low concentrations in aqueous solution. The route of quick cultivating microalgal biofilm on marine structures through constructing biological layer on their surfaces would give insight into developing new techniques for removing low concentration heavy metal ions from water for environmental bioremediation.

Sustainable grafted chitosan-dialdehyde cellulose with high adsorption capacity of heavy metal.

A novel adsorbent was prepared using a backbone comprising chemically hybridized dialdehyde cellulose (DAC) with chitosan via Schiff base reaction, followed by graft copolymerization of acrylic acid. Fourier transform infrared spectroscopy (FTIR) confirmed the hybridization while scanning electron microscopy (SEM) revealed intensive covering of chitosan onto the surface of DAC. At the same time, energy dispersive X-ray (EDX) proved the emergence of nitrogen derived from chitosan. The X-ray diffraction (XRD) indicated that the crystallinity of the backbone and graft copolymer structures was neither affected post the hybridization nor the grafting polymerization. The adsorbent showed high swelling capacity (872%) and highly efficient removal and selectivity of Ni2+ in the presence of other disturbing ions such as Pb2+ or Cu2+. The kinetic study found that the second-order kinetic model could better describe the adsorption process of (Cu2+, Ni2+) on the graft copolymer. In contrast, the first-order kinetic model prevails for the binary mixture (Pb2+, Ni2+). Moreover, the correlation coefficient values for the adsorption process of these binary elements using Langmuir and Freundlich isotherms confirmed that the developed grafted DAC/chitosan exhibits a good fit with both isotherm models, which indicates its broadened and complicated structure. Furthermore, the grafted DAC/chitosan exhibited high efficient regeneration and high adsorption capacity for Pb2+, Cu2+ and Ni2+.

Design of amphoteric MOFs-cellulose based composite for wastewater remediation: Adsorption and catalysis.

Water pollution remains a serious problem for aquatic organism and human beings. Developing an efficient material which can simultaneously remove and convert pollutants into low or no harmful compounds is an essential issue. Targeting at this goal, a multifunctional and amphoteric wastewater treatment material of Co-MOF and functionalized cellulose-based composite (CMC/SA/PEI/ZIF-67) was designed and prepared. Carboxymethyl cellulose (CMC) and sodium alginate (SA) were selected as support to construct an interpenetrating network structure and made it crosslinked with polyethyleneimine (PEI) for further in situ growth of ZIF-67 with good dispersion. The material was characterized using an appropriate set of spectroscopic and analytical techniques. When applied in the adsorption of heavy metal oxyanions with no adjustment of pH, the adsorbent could completely decontaminate Cr(VI) at both low and high initial concentrations with good reduction rates. The adsorbent maintained good reusability after five cycles. Meanwhile, the cobalt species of CMC/SA/PEI/ZIF-67 can activate peroxymonosulfate to generate high oxidizing substances (such as SO4-· and ·OH- radicals) to degrade cationic rhodamine B dye within 120 min, thus indicating the amphoteric and catalytic nature of our CMC/SA/PEI/ZIF-67 adsorbent. The mechanism of the adsorption and catalytic process was also discussed based with the assistance of different characterization analysis.

Synthesis of Chemically Modified Acid-Functionalized Multiwall Carbon Nanotubes with Benzimidazole for Removal of Lead and Cadmium Ions from Wastewater.

In this work, acid-functionalized multiwalled carbon (MWCNTs-CO2H) nanotube was successfully functionalized with a heterocyclic scaffold, namely benzimidazole, to give novel functionalized multiwalled carbon nanotubes (BI@MWCNTs). Then, FTIR, XRD, TEM, EDX, Raman spectroscopy, DLS, and BET analyses were used to characterize the synthesized BI@MWCNTs. The effectiveness of the adsorption of two heavy metal ions, Cd2+ and Pb2+, in single metal and mixed metal solutions on the prepared material was investigated. Influencing parameters for the adsorption method, for example duration, pH, starting metal concentration, and BI@MWCNT dosage, were examined for both metal ions. Moreover, adsorption equilibrium isotherms fit with the Langmuir and Freundlich models perfectly, while the intra-particle diffusion models provide pseudo-second order adsorption kinetics. The adsorption of Cd2+ and Pb2+ ions onto BI@MWCNTs revealed an endothermic and a spontaneous method with great affinity as a result of the negative values of Gibbs free energy (ΔG) and the positive values of enthalpy (ΔH) and entropy (ΔS). Both Pb2+ and Cd2+ ions were completely eliminated from aqueous solution (100 and 98%, respectively) using the prepared material. Additionally, BI@MWCNTs have a high adsorption capacity and were regenerated in a simple way and reused for six cycles, which make them a cost-effective and efficient absorbent for the removal of such heavy metal ions from wastewater.

Epoxied SiO2 nanoparticles and polyethyleneimine (PEI) coated polyvinylidene fluoride (PVDF) membrane for improved oil water separation, anti-fouling, dye and heavy metal ions removal capabilities.

Epoxied SiO2 nanoparticles and polyethyleneimine (PEI) was used to coating polyvinylidene fluoride (PVDF) membrane for improved anti-fouling, oil water separation, dye and heavy metal ions removal capabilities. Characterization of the modified membrane revealed that the hydrophilic coating layer was applied onto the PVDF substrate successfully. The modified membrane can exhibit a high degree of superhydrophilicity and underwater superoleophobicity. Consequently over 98% of the oil was retained when this membrane was used in oil water separation. The hydrophilic coating layer enhanced the membrane antifouling performance, and its flux recovery rate reached 96.3% after filtration and washing with bovine serum protein solution (BSA). In addition, the modified membrane presented the ability to adsorb organic dyes and heavy metal ions in water and reject them via filtration. Most importantly, the crosslinking reaction between the epoxied SiO2 nanoparticles and PEI imparts a high degree of stability to the coating layer. Thanks to the simple fabrication method and multifunctional performances of the coating layer described in this report, it may be used to modify other substrates.

Polyaniline Modified CNTs and Graphene Nanocomposite for Removal of Lead and Zinc Metal Ions: Kinetics, Thermodynamics and Desorption Studies.

A novel polyaniline-modified CNT and graphene-based nanocomposite (2.32-7.34 nm) was prepared and characterized by spectroscopic methods. The specific surface area was 176 m2/g with 0.232 cm3/g as the specific pore volume. The nanocomposite was used to remove zinc and lead metal ions from water; showing a high removal capacity of 346 and 581 mg/g at pH 6.5. The data followed pseudo-second-order, intraparticle diffusion and Elovich models. Besides this, the experimental values obeyed Langmuir and Temkin isotherms. The results confirmed that the removal of lead and zinc ions occurred in a mixed mode, that is, diffusion absorption and ion exchange between the heterogeneous surface of the sorbent containing active adsorption centers and the solution containing metal ions. The enthalpy values were 149.9 and 158.6 J.mol-1K-1 for zinc and lead metal ions. The negative values of free energies were in the range of -4.97 to -26.3 kJ/mol. These values indicated an endothermic spontaneous removal of metal ions from water. The reported method is useful to remove the zinc and lead metal ions in any water body due to the high removal capacity of nanocomposite at natural pH of 6.5. Moreover, a low dose of 0.005 g per 30 mL made this method economical. Furthermore, a low contact time of 15 min made this method applicable to the removal of the reported metal ions from water in a short time. Briefly, the reported method is highly economical, nature-friendly and fast and can be used to remove the reported metal ions from any water resource.

Activated Biocarbons Obtained from Plant Biomass as Adsorbents of Heavy Metal Ions.

This paper deals with the adsorption of heavy metal ions on the surface of carbonaceous materials obtained via the chemical activation of biomass. Waste plum stones, pine sawdust and horsetail herb were used as the precursors of carbonaceous adsorbents. The effect of the precursor type and preparation procedure on the physicochemical properties of activated biocarbons and their sorption abilities towards Pb(II) and Cu(II) ions have been checked. The obtained micro-mesoporous activated biocarbons were characterized by determination of elemental composition and ash content, the number of surface functional groups and pH of water extracts as well as textural study based on low temperature nitrogen adsorption/desorption and scanning electron microscopy. Additionally, the electrokinetic studies including solid surface charge density and zeta potential determination were performed. Moreover, the adsorption data modelling (equilibrium and kinetics), XPS results analysis and comparison of parameters characterizing electrical double layer formed at the solid-liquid interface enabled the specification of the mechanism of heavy metals binding with the activated biocarbons surface. The maximum adsorption capacity towards copper and lead ions (177.5 and 178.1 mg/g, respectively) was found for plum stone-based activated biocarbon. For all carbonaceous materials, better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. In turn, a better fit of the kinetics data was obtained using the pseudo-second order model.

Data that support the use of agro-industrial residues from orange peel and sugarcane bagasse for the production of carbonaceous structures and their application in the removal of metal ions.

This document contains additional information for the production of activated carbons (AC) and carbon foams (CF) from agroindustrial wastes, orange peel (OP) and sugarcane bagasse (SCB). In particular, a set of data is presented for the characterization of carbonaceous structures (AC and CF) and their application in the removal of metallic ions contained in polluted waters. The adsorbent materials were obtained combining chemical and physical activation processes. Data presented here included characterization of AC and CF using dynamic light scattering (DLS), BET (Brunauer, Emmet and Teller) surface area analysis, Barrett-Joyner-Halenda (BJH) method to assess pore size distribution and zeta potential (ζ) to evaluate electrokinetic potential of carbonaceous structures. In addition, energy dispersive spectroscopy (SEM/EDS) to identify heavy metals on the surface of carbonaceous materials is shown and complementary adsorption capacity data for metal ion removal are presented in the paper. The data can be used as a reference to promote reuse of agroindustrial wastes and provide added value; particularly for the synthesis of carbonaceous structures applied to the water purification.

Insights into the mechanically resilient, well-balanced polymeric membranes by incorporating Rhizophora mucronata derived activated carbon for sustainable wastewater decontamination.

In this study, hydrophilic activated carbon has been prepared and used to synthesize innovative activated carbon/polysulfone mixed matrix membranes (MMMs). These membranes were investigated in terms of membrane morphology, hydrophilicity, antifouling ability, and metal ions rejection. The activated carbon (AC) was prepared from a simple chemical activation method using Rhizophora mucronata propagules, which are rich in aerenchyma cells and possess a high surface area. The hydrophilicity of the MMMs is enhanced by the incorporation of activated carbon, which is confirmed by the measurement of equilibrium water contact angle, water uptake and pure water flux. The optimized concentration of 0.625 wt% activated carbon (A2) incorporated mixed matrix membrane exhibits better rejection efficiencies of 98 ± 0.5%, 99 ± 0.5%, 92 ± 2%, and 44 ± 1% for Pb+2, Cd+2, Hg+2, and F- with the permeate flux of 28.27, 31.88, 33.21, 43.82 L/m2/h, respectively. The fabricated mixed matrix membranes demonstrated an excellent flux recovery ratio and reversible fouling, when filtrating a mixed feed solution containing 200 ppm BSA, 10 ppm Pb+2 and 10 ppm Cd+2. The optimized A2 membrane showed excellent long-term stability up to 120 h without compromising in permeate flux and rejection efficiency. Finally, a numerical investigation using a usual transport model has shown that dielectric exclusion was the most probable mechanism that can physically explain experimental trends.

Metal organic framework UiO-66 incorporated ultrafiltration membranes for simultaneous natural organic matter and heavy metal ions removal.

In this work, a new type of UiO-66 incorporated polysulfone (PSf) ultrafiltration (UF) membranes was fabricated to enhance antifouling properties and heavy metal ions removal efficiency. The UF membranes incorporating different loadings of the UiO-66 filler were prepared via the classical phase inversion process. These membranes unveiled enhanced hydrophilicity, porosity, water uptake, zeta potential, mechanical strength, permeability, and HA removal ratios due to the incorporation of hydrophilic UiO-66 fillers. Particularly, HA rejection ratios were observed to be approximately 93% for all the modified membranes, which was attributed to electrostatic repulsion interactions between the hydrophilic groups of HA and UiO-66. Moreover, the antifouling abilities of the modified membranes were evaluated and found to be much better with a high flux recovery ratio (FRR) of about 88% when compared to the blank PSf membrane (only around 34%). Moreover, the UiO-66 incorporated membranes were highly-effective in the removal of contaminants like heavy metal ions (Sr2+, Pb2+, Cd2+, and Cr6+) and HA at the same time. Overall, the PSf UF membranes incorporating UiO-66 opened up a new avenue to enhance the membrane hydrophilicity, permeability, antifouling properties as well as heavy metal ions removal abilities.

Facile immobilization of ethylenediamine tetramethylene-phosphonic acid into UiO-66 for toxic divalent heavy metal ions removal: An experimental and theoretical exploration.

By the facile immobilization of ethylenediamine tetramethylene-phosphonic acid (EDTMPA) onto the surface and into the defects of UiO-66, a stable and efficient adsorbent named UiO-66-EDTMPA was obtained for the first time. In terms of removing aqueous heavy metal ions (Pb2+, Cd2+, Cu2+), the maximum adsorption capacities of UiO-66-EDTMPA reached 558.67, 271.34 and 210.89 mg/g, which were 8.77 (Pb2+), 5.63 (Cd2+) and 5.19 (Cu2+) times higher than raw UiO-66 respectively. The adsorption behavior of three heavy metal ions on UiO-66 and UiO-66-EDTMPA were investigated and compared through batch control experiments and theoretical studies. The main factors on adsorption progress (i.e., the dosage of EDTMPA, pH, ionic strength, co-existing ions, initial concentration, contact time, temperature) were explored, and the critical characterization (i.e., SEM, TEM, XRD, FT-IR, TG-DTG, XPS, N2 adsorption-desorption test) were performed. Molecular dynamics (MD) simulation (radial distribution functions (RDF) and mean square displacement (MSD)) were also applied to reveal the adsorption behavior. Besides, two new quantum chemical analyses (Hirshfeld surface and independent gradient model (IGM)) were introduced into the interaction analysis between UiO-66 and EDTMPA. The complete results showed that (1) where the hydrogen bond and (vdW) connect EDTMPA to UiO-66. (2) The coordination between O, N atoms of EDTMPA and heavy metal ions (Pb2+, Cd2+, Cu2+) resulted in spontaneous adsorption. (3) The adsorption behavior agreed with Langmuir and pseudo-second-order model, endothermic reaction. In addition, the desorption and reusability study showed promising stable and sustainable performance. This work has some guiding significance for the experimental and theoretical study of removing heavy metal ions from aqueous solutions by MOF or modified MOF materials.

Hybrid capacitive deionization of NaCl and toxic heavy metal ions using faradic electrodes of silver nanospheres decorated pomegranate peel-derived activated carbon.

Capacitive deionization (CDI) is an evolving technology for eradicating salt and toxic heavy metal ions from brackish wastewater. However, traditional CDI electrodes have lower salt adsorption capacity and inadequate adsorption of selective metal ions for long-term operations. Herein, Ag nanospheres incorporated pomegranate peel-derived activated carbon (Ag/P-AC) was prepared and implied to the CDI process for removing NaCl, toxic mono-, di-, and trivalent metal ions. Morphological analysis revealed that the 80-100 nm-sized Ag nanospheres were uniformly decorated on the surfaces of P-AC nanosheets. The Ag/P-AC has a higher specific surface area (640 m2 g-1), superior specific capacitance (180 F g-1 at 50 mV s-1) and a lower charge transfer resistance (0.5 Ω cm2). CDI device was fabricated by Ag/P-AC as an anode, which adsorbed anions and P-AC as cathode for adsorption of positively charged ions at 1.2 V in an initial salt concentration of 1000 mg L-1. An asymmetric Ag/P-AC//P-AC exhibited a maximum NaCl adsorption capacity of 36 mg g-1 than symmetric P-AC//P-AC electrodes (22.7 mg g-1). Furthermore, Pb(II), Cd(II), F-, and As(III) ions were successfully removed from simulated wastewater by using Ag/P-AC//P-AC based CDI system. These asymmetric CDI-electrodes have an excellent prospect for the removal of salt and toxic contaminants in industrial wastewater.

Highly efficient and selectivity removal of heavy metal ions using single-layer NaxKyMnO2 nanosheet: A combination of experimental and theoretical study.

Manganese oxides (MnO2) are widely applied in heavy metal ions removal due to their low-cost, environmental-friendly and biocompatibility. However, the adsorption capacity of MnO2 need to be further improved to satisfy the demand of practical application. Herein, a highly dispersed single layer NaxKyMnO2 nanosheet was synthesized by a facile wet-chemical method with sodium dodecyl sulfonate as surfactant. The high surface specific area, excellent dispersibility and abundant oxygen vacancies endowed NaxKyMnO2 nanosheets with potential in heavy metal ions adsorption. The adsorption experiments results showed that NaxKyMnO2 nanosheets possessed high efficiency and selectivity towards lead ion (Pb2+) with a high adsorption capacity of 2091.8 µmol g-1. The NaxKyMnO2 also showed an excellent reusability with the removal rate of 95.4% for Pb2+ even after five cycles. Moreover, both the theoretical calculation and experimental data illustrated that the single layer NaxKyMnO2 nanosheets possess high selectivity to Pb2+ adsorption.

Composite cryo-beads of chitosan reinforced with natural zeolites with remarkable elasticity and switching on/off selectivity for heavy metal ions.

Combining ion-imprinting technology with pH-dependent adsorptive features of acid- or salt-activated zeolites brings up the opportunity to develop composite polymer materials with 'desired' sorption properties and performances. In this respect, we present here Co2+-imprinted composite cryo-beads with switching on/off selectivity towards the template ions, engineered by selecting the appropriate zeolite-treatment conditions and/or controlling the initial sorption pH values. Co2+ chelating efficiency of all cryo-beads was investigated either at pH 4 or 6 depending on zeolite conditioning strategy. The maximum sorption capacity values of ion-imprinted cryo-beads were from about 5 up to 7 times higher compared with those of non-imprinted ones. Under competitive conditions (Cu2+, Ni2+, Fe2+ and Cd2+ ions), the change of pH value from 4 to 6 resulted in a remarkable quenching of Co2+ selectivity generated by the zeolite shift from the H+-form to the Na+-form. The presence of zeolites within cryogel matrix generated composites with outstanding elasticity that allows the instant recovery of gels after full compression. These results indicate that the cryogel-type composites can be successfully re-used in separation processes for several times without losing their features.

Carboxylated cellulose cryogel beads via a one-step ester crosslinking of maleic anhydride for copper ions removal.

In this study, we developed a one step protocol to prepare highly carboxylated and chemically crosslinked cellulose nanofibril (CNF) cryogel beads using maleic anhydride (MA). Fourier transform infrared spectroscopy (FTIR) and conductometric-potentiometric titration results confirmed the presence of carboxyl groups and ester linkages produced simultaneously during the ring open reaction of MA, yielding a carboxylic content of up to 2.78 mmol/g. The effect of CNF concentration on the morphology and wet mechanical strength of the crosslinked cryogel beads were also investigated, and results suggested that higher CNF concentration yielded a compact network that displayed a maximum compressive stress of 2800 Pa at 60 % strain. In addition, the heavy metal ions (i.e., Cu (II)) removal capacity, kinetics, mechanism as well as the recyclability of the resulted CNF-MA cryogel beads were examined.

Heavy metal removal from water by adsorption using a low-cost geopolymer.

In the present study, a geopolymer from dolochar ash was synthesized and used for the removal of heavy metal ions such as Co(II), Ni(II), Cd(II), and Pb(II) from the aqueous solution through the adsorption process. The geopolymer was characterized by a series of analytical techniques. The XRD pattern revealed the loss of dolochar ash crystallinity on geoploymerization. The peak at 982 cm-1 observed in the FTIR spectrum due to Si-O-Si and Si-O-Al bonds confirmed the formation of geopolymer. BET surface area analyses indicated the mesoporous nature of the sample. The adsorption experiments revealed the higher removal efficiency of the geopolymer in comparison with the feed dolochar ash. The effects of different experimental factors such as pH, temperature, reaction time, and initial concentration of metal ions on metal uptake efficiency were evaluated to optimize the removal efficiency. The maximum removal of 98-99% was achieved when the pH, temperature, and initial metal ion concentration were 7.8, 343 K, and 10 ppm, respectively. The adsorption process followed the pseudo-second-order rate equation and validated the Langmuir adsorption model. Thermodynamic parameters such as ΔH, ΔS, and ΔG confirmed that the process to be spontaneous and endothermic. This geopolymer was found to compete efficiently with many adsorbents reported in the literature for water treatment.

A novel layer-by-layer heterogeneous cation exchange membrane for heavy metal ions removal from water.

A novel layer-by-layer (LbL) cation exchange membrane was prepared for heavy metal ions removal from water via electrodialysis. LBL membranes fabricated by coating of [chitosan-co-activated carbon nanoparticles] layer on polyvinyl chloride-based heterogeneous cation exchange membrane. Betterment in adherence of layers was achieved through glutaraldehyde cross linking. FTIR, FESEM, 3D-surface images and BET analysis were used for LBL membrane characterization. Membrane surface hydrophilicity, flux, membrane potential, transport number, and their permselectivity were studied. FTIR spectra confirm LbL formation decisively. FESEM images and BET analysis demonstrated that coating of second layer on PVC membrane led to a compact structure. LbL membrane showed smoother and more hydrophilic surface compared to pristine membrane. The transport number and permselectivity increased by deposition of second layer whereas sodium flux showed up-down trend. ED experiment showed good ability in heavy metal ions removal for LBL membrane that follows (Cu2+> Ni2+> Pb2+) sequence. EDX analysis showed a competitive adsorption for heavy metal ions on LBL membrane as (Pb2+> Cu2+≥Ni2+). The effect of ultrasonic waves on regeneration of fouled membranes by heavy metals was investigated. The results showed improved performance for the regenerated membrane. Mechanical resistance also improved by utilizing of ACNs in chitosan layer.

Ion-Induced Synthesis of Alginate Fibroid Hydrogel for Heavy Metal Ions Removal.

Design and synthesis of environmentally friendly adsorbents with high adsorption capacities are urgently needed to control pollution of water resources. In this work, a calcium ion-induced approach was used to synthesize sodium alginate fibroid hydrogel (AFH). The as-prepared AFH has certain mechanical strength, and the mechanical strength is enhanced especially after the adsorption of heavy metal ions, which is very convenient for the recovery. AFH exhibited excellent adsorption performances for Cu2+, Cd2+, and Pb2+ ions and displayed very high saturated adsorption capacities (Qe) of 315.92 mg·g-1 (Cu2+), 232.35 mg·g-1 (Cd2+), and 465.22 mg·g-1 (Pb2+) with optimized pH values (3.0-4.0) and temperature (303 K). The study of isotherms and kinetics indicated that adsorption processes of heavy metal ions fitted well with the pseudo-second-order kinetics model and the Langmuir model. Pb2+ was found to have the strongest competitiveness among the three heavy metal ions. Thus, AFH has great application prospects in the field of heavy metal ions removing from wastewater.

Selective heavy metal removal and water purification by microfluidically-generated chitosan microspheres: Characteristics, modeling and application.

Many industrial wastewater streams contain heavy metals, posing serious and irreversible damage to humans and living organisms, even at low concentrations due to their high toxicity and persistence in the environment. In this study, high-performance monodispersed chitosan (CS) microspheres were prepared using a simple microfluidic method and evaluated for metal removal from contaminated water. Batch experiments were carried out to evaluate the adsorption characteristics for the removal of copper ions, one representative heavy metal, from aqueous solutions. The inherent advantages of microfluidics enabled a precise control of particle size (CV = 2.3%), while exhibiting outstanding selectivity towards target ions (adsorption capacity 75.52 mg g-1) and fair regeneration (re-adsorption efficiency 74% after 5 cycles). An integrated adsorption mechanism analytic system was developed based on different adsorption kinetics and isotherms models, providing an excellent adsorption prediction model with pseudo-second order kinetics (R2 = 0.999), while the isotherm was fitted best to the Langmuir model (R2 = 0.998). The multi-step adsorption process was revealed via quantitative measurements and schematically described. Selective adsorption performance of CS microspheres in the present of other competitive metal ions with different valence states has been demonstrated and studied by both experimental and density functional theory (DFT) analysis.