Adsorptive removal of phosphate from water with biochar from acacia tree modified with iron and magnesium oxides.

A novel biochar (BC) from Acacia tortilis trees pruning waste was synthesized and tested for the removal of phosphate from aqueous solutions. The BC was prepared by calcination at 600 °C and doped with Fe3O4 and MgO by hydrothermal process. The presence of iron and magnesium ions in the modified BC was confirmed by EDS analysis and X-ray diffraction (XRD) methods. Both unmodified and doped BCs were tested for phosphate removal from synthetic 1-500 ppm aqueous solutions. While the unmodified BC did not show any significant removal of phosphate from aqueous solutions, the modified BC almost completely removed phosphate from water. The enhancement in removal efficiency is due to an increase in the overall surface charge and surface area of BC as a result of doping with Fe3O4 and MgO salts. The average porosity and BET surface area corresponding to the plain BC increased by more than 20% from 322 to 394 m2/g after modification by impregnation with iron oxide and magnesium oxide. The modificaiton of BC with Fe3O4 and MgO nanoparticles was observed to increase the point of zero electric charge (PZC) from pH 3.4 (corresponding to plain BC) to pH 5.3 (corresponding to modified BC). The adsorption process was very fast and a phosphate removal value of 82.5% was reached only after 30 min of adsorption, while the removal efficiency after 4 h of adsorption was 97.5%. The rapid removal efficiency in short contact time is attributed to the high surface area of BC and strong bonding between the modified BC surface and PO43- ions. The highest adsorption capacity was observed to correspond to 98.5 mg/g which was achieved at PO43- concentration of 500 ppm and pH 8.5. Moreover, after fitting the adsorption data onto four of the most widely used adsorption isotherm models, the adsorption of PO43- onto BC can be better described by the Langmuir isotherm model.

Antimicrobial activity of ZnO-Ag-MWCNTs nanocomposites prepared by a simple impregnation-calcination method.

Zinc oxide (ZnO) nanorods and ZnO nanostructures composited with silver (Ag) and multi-walled carbon nanotubes (MWCNTs) have been synthesized by a simple impregnation-calcination method and have been shown to be suitable for use as antimicrobial agents. The preparation method used for composite materials is very simple, time-effective, and can be used for large-scale production. Several analytical techniques, including X-ray diffraction (XRD), scanning electron spectroscopy (SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and Fourier transmission infrared spectroscopy (FTIR), have been used to characterize the prepared ZnO-Ag-MWCNT composite materials. The effects on structural, morphological, and antimicrobial properties of (ZnO)100-x (Ag)x nanocomposites at various weight ratios (x = 0, 5, 10, 30, and 50 wt%) have been investigated. The antimicrobial properties of ZnO composited with Ag nanoparticles and MWCNTs towards both gram-positive and gram-negative bacteria species were studied. The effect of raw MWCNTs and MWCNTs composited with ZnO and Ag on the cell morphology and chemical composition of Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) was studied by SEM and EDS, respectively. It was found that composite materials made of ZnO-Ag-MWCNTs exhibit greater antibacterial activities toward the microorganisms E. coli and S. aureus than ZnO-Ag, which could be beneficial for efficient antimicrobial agents in water and air treatment applications.

Oxidized carbide-derived carbon as a novel filler for improved antifouling characteristics and permeate flux of hybrid polyethersulfone ultrafiltration membranes.

Polyethersulfone (PES) is a widely used polymer for ultrafiltration (UF) membrane fabrication. In the current study, carbide-derived carbon (CDC) oxidized by acid treatment was utilized as a filler to fabricate a novel PES composites UF membranes. The successful oxidation of CDC was validated from presence of oxygen containing functional groups and improved oxygen content, from 5.08 at.% for CDC to 26.22 at.% for oxidized CDC (OCDC). The OCDC PES UF membranes were prepared at different loadings of OCDC between 0.5 and 3.0 wt%. The membrane porosity, pore size and surface free energy found to be improved while a noticeable reduction in water contact angle was observed with OCDC loading implying the improved hydrophilicity of PES membranes. Consequently, the pure water flux found to improve from 151.6 to 569.6 (L/(m2. h)) for the 3.0 wt% modified OCDC membrane (M-3) which is 3.8 folds of the bare PES membrane. The antifouling characteristics were evaluated by humic acid (HA) filtration. The results revealed a significant enhancement in HA rejection with OCDC loading, the highest rejection was 96.8% for M-3 membrane. Additionally, the adsorption capacity of OCDC modified membranes found to decrease with OCDC loading indicating improved rejection of HA from the membrane surface. Moreover, M-3 demonstrated the maximum flux recovery ratio (FRR) of 92.3%. Reusability of the fabricated membranes was evaluated by deionized water/humic acid cycling filtration. The FRR was higher than 86.7% over three cycles of pure water/HA filtration for 140 min, indicated the excellent stability and reusability of the membranes. Overall, the OCDC was an effective filler for enhancing the PES UF membranes antifouling and permeability properties.

XPS, structural and antimicrobial studies of novel functionalized halloysite nanotubes.

A novel robust preparation method based on thermal salt decomposition has been elaborated for synthesis of halloysite nanotubes (HNTs) impregnated with silver and iron oxide nanoparticles. The developed method is simple, time-effective, and can be employed for large scale material fabrication. Different characterization techniques, including X-ray diffraction (XRD), scanning and transmission electron spectroscopy (SEM and TEM) and energy dispersive X-ray spectroscopy (EDS) have been used to characterize the functionalized HNTs composite materials. Surface elemental and chemical state analysis was conducted using X-ray photoelectron spectrometer (XPS). The functionalized HNTs exhibit enhanced total surface area (by 17.5%) and pore volume (by 11%) compare to the raw HNTs calculated by using the Brunauer-Emmett-Teller (BET) method. It was shown that functionalized HNTs possess high antimicrobial properties towards both gram- positive and gram-negative bacteria species. The enhanced surface area and bactericidal properties of functionalized HNTs could be beneficial for employing of the prepared material as low cost filtration media for water treatment applications. Molecular dynamics (FPMD) were performed to obtain insights about possible physiochemical mechanisms for chemical adsorption and on the HNT thermal stability.

A Comparative Analysis of the Effect of Carbonaceous Nanoparticles on the Physicochemical Properties of Hybrid Polyethersulfone Ultrafiltration Membranes.

Numerous studies have been previously reported on the use of nanoscale carbonaceous fillers, such as multi-walled carbon nanotubes (MWCNTs) and graphene oxide (GO), in polymeric ultrafiltration (UF) membranes; however, no insight has been clearly reported on which material provides the best enhancements in membrane performance. In this study, a comparative analysis was carried out to establish a comprehensible understanding of the physicochemical properties of hybrid polyethersulfone (PES) UF membranes incorporated with MWCNTs and GO nanoparticles at various concentrations. The hybrid membranes were prepared via the non-solvent-induced phase separation process and further characterized by field emission scanning electron microscopy and atomic force microscope (AFM). The AFM images showed homogeneous membrane surfaces with a reduction in the membrane surface roughness from 2.62 nm for bare PES to 2.39 nm for PES/MWCNTs and to 1.68 nm for PES/GO membranes due to improved hydrophilicity of the membranes. Physicochemical properties of the hybrid PES membranes were assessed, and the outcomes showed an enhancement in the porosity, pore size, water contact angle, and water permeability with respect to nanoparticle concentration. GO-incorporated PES membranes exhibited the highest porosity, pore size, and lowest contact angle as compared to PES/MWCNTs, indicating the homogeneous distribution of nanoparticles within the membrane structure. PES/MWCNTs (0.5 wt.%) and PES/GO (1.0 wt.%) hybrid membranes exhibited the highest water flux of 450.0 and 554.8 L m-2 h-1, respectively, at an applied operating pressure of 1 bar. The filtration and antifouling performance of the PES hybrid membranes were evaluated using 50 mg L-1 of humic acid (HA) as a foulant at pH = 7. Compared to the bare PES membrane, the MWCNTs and GO-incorporated PES hybrid membranes exhibited enhanced permeability and HA removal. Moreover, PES/MWCNTs (0.5 wt.%) and PES/GO (1 wt.%) hybrid membranes reported HA rejection of 90.8% and 94.8%, respectively. The abundant oxygen-containing functional groups in GO-incorporated PES membranes resulted in more hydrophilic membranes, leading to enhanced permeability and fouling resistance. The antifouling properties and flux recovery ratio were improved by the addition of both nanoparticles. Given these findings, although both MWCNTs and GO nanoparticles are seen to notably improve the membrane performance, PES membranes with 1 wt.% GO loading provided the highest removal of natural organic matter, such as HA, under the same experimental conditions.

Preparation and Characterization of Polysulfone Membranes Reinforced with Cellulose Nanofibers.

The mechanical properties of polymeric membranes are very important in water treatment applications. In this study, polysulfone (PSF) membranes with different loadings of cellulose nanofibers (CNFs) were prepared via the phase inversion method. CNF was characterized through transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The pore morphology, mechanical properties, membrane performance and hydrophilicity of pure PSF membranes and PSF/CNF membranes were investigated. The changes in membrane pore structure with the addition of different CNF contents were observed using SEM images. It was shown that the calculated membrane pore sizes correlate with the membrane water fluxes. The pure water flux (PWF) of fabricated membranes increased with the addition of CNFs into the PSF matrix. It was shown that the optimal CNF loading of 0.3 wt.% CNF improved both the elastic modulus and yield stress of the PSF/CNF membranes by 34% and 32%, respectively (corresponds to values of 234.5 MPa and 5.03 MPa, respectively). This result indicates a strong interfacial interaction between the PSF matrix and the reinforced nanofibers. The calculated compaction factor (CF) showed that the membrane resistance to compaction could be improved with CNF reinforcement. Compared to pure PSF membrane, the hydrophilicity was significantly enhanced with the incorporation of 0.1 wt.%, 0.2 wt.% and 0.3 wt.% CNF, as shown by the water contact angle (WCA) results. It can be concluded that CNFs are homogeneously dispersed within the PSF matrix at CNF loading less than 0.5 wt.%.

Carbide-derived carbon as an extraordinary material for the removal of chromium from an aqueous solution.

In the present work, the adsorptive removal of chromium (Cr) from water by carbide-derived carbon (CDC) was investigated. The morphology and structure of the CDC were characterized by using FTIR, SEM, TEM, XRD, and N2 adsorption-desorption measurements. The effect of adsorption parameters including contact time, initial Cr concentration, temperature, initial solution pH, and CDC dosage was examined on the removal of Cr ions. The kinetic analysis revealed that the experimental data on the removal of Cr ions on CDC is well correlated with the pseudo-second order kinetic model (with R2 > 0.999), while the equilibrium data were fitted by the Redlich-Peterson isotherm model (with R2 > 0.992). The Langmuir and Sips models were also in good compliance with the equilibrium data, indicating a monolayer coverage of Cr ions onto the CDC surface with some heterogeneous active adsorption sites. The CDC revealed a notable Langmuir adsorption capacity of 159.1 mg/g for Cr ions at pH 6 and room temperature. The thermodynamic analysis illustrated that the Cr ions elimination by CDC is a feasible adsorption process and endothermic in nature. After five adsorption/desorption cycles, less than 18% reduction in the adsorption capacity was obtained indicating the stability and reusability of the CDC. Moreover, the CDC demonstrated an excellent potential in removing the Cr ions from real brackish water. According to the adsorption data, both physical and chemical adsorption processes occurred, and the adsorption was mainly controlled by electrostatic interactions with a possible reduction of hexavalent Cr to trivalent Cr at acidic conditions.

A Review on the Modeling of the Elastic Modulus and Yield Stress of Polymers and Polymer Nanocomposites: Effect of Temperature, Loading Rate and Porosity.

Porous polymer-based nanocomposites have been used for various applications due to their advantages, including multi-functionalities, easy and known manufacturability, and low cost. Understanding of their mechanical properties has become essential to expand the nanocomposites' applications and efficiency, including service-life, resistance to different loads, and reliability. In this review paper, the focus is on the modeling of the mechanical properties of porous polymer-based nanocomposites, including the effects of loading rates, operational temperatures, and the material's porosity. First, modeling of the elastic modulus and yield stress for glassy polymers and polymer reinforced by nanofillers are addressed. Then, modeling of porosity effects on these properties for polymers are reviewed, especially via the use of the well-known power-law approach linking porosity to elastic modulus and/or stress. Studies related to extending the mechanical modeling to account for porosity effects on the elastic modulus and yield stress of polymers and polymer-nanocomposites are discussed. Finally, a brief review of the implementation of this modeling into 3D computational methods to predict the large elastic-viscoplastic deformation response of glassy polymers is presented. In addition to the modeling part, the experimental techniques to measure the elastic modulus and the yield stress are discussed, and applications of polymers and polymer composites as membranes for water treatment and scaffolds for bone tissue engineering are addressed. Some modeling results and validation from different studies are presented as well.

Kinetic and thermodynamic investigations of surfactants adsorption from water by carbide-derived carbon.

The objective of the study is to investigate the potential of carbide-derived carbon (CDC) for the adsorptive removal of nonionic t-octylphenoxy poly ethoxy ethanol (TX-100), anionic sodium dodecylbenzene sulfonate (SDBS) and cationic 1-hexadecylpyridinium bromide (HDPB) surfactants from water. The CDC was characterized using TEM, SEM, FTIR, BET, EDS, XPS methods and zeta potential measurements. The effects of adsorption parameters included initial surfactant concentration, contact time, temperature, and pH of the feed solution were evaluated. The adsorption capacity and mechanism were determined by modeling the isotherm, kinetic and thermodynamic data. The kinetics results demonstrated that the adsorption of the surfactant by CDC obeys the pseudo 2nd order model. The thermodynamic results have shown that surfactants adsorption by CDC is an endothermic and spontaneous process. The Sips model agreed with the adsorption isotherm data of SDBS with R2 of 0.987, while both Freundlich and Redlich-Peterson models comply well with adsorption data for TX-100 and HDPB. The hydrophobic and electrostatic interactions were found the dominant mechanisms of the adsorption of the surfactant by CDC. The adsorption capacities of CDC were found to be 442.4, 462.0 and 578.4 mg/g for SDBS, HDPB and TX-100, respectively.

Review of phosphate removal from water by carbonaceous sorbents.

In the last decades, phosphate is considered the main cause of eutrophication and has received substantial attention from the scientific community. Phosphate is a major pollutant that deteriorates water quality, which has been increasing in water resources, primarily due to the increasing global population and corresponding activities. Adsorption technology is amongst the different technologies used to decrease the phosphate levels in water, and has been found to be highly effective even at low phosphate concentrations. Carbonaceous materials and their composites have been widely used for phosphate removal due to their exceptional surface properties and high phosphate sorption capacity. Considering the importance of the topic, this study reviews the reported literature in the field of adsorptive removal of phosphate over various carbon-based adsorbents such as activated carbon, charcoal, graphene, graphene oxide, graphite and carbon nanotubes. Moreover, insights into the adsorption behaviour, experimental parameters, mechanisms, thermodynamics, effect of coexisting ions and the possible desorption processes of phosphate onto modified and unmodified carbonaceous adsorbents are also considered. Finally, research challenges and gaps have been highlighted.

Carbide Derived Carbon (CDC) as novel adsorbent for ibuprofen removal from synthetic water and treated sewage effluent.

PURPOSE: Pharmaceuticals are becoming one of the largest environmental concerns when it comes to the water treatment industry. Increased usage of these chemicals poses a serious risk to ecology and human health due to their leakage into surface waters. In the present study, carbide derived carbon (CDC) was used for the first time as a new adsorbent to remove ibuprofen from synthetic water and wastewater effluent. METHODS: The morphology, chemical composition, surface area and surface charge of the CDC particles were investigated using the transmission electron microscopy, scanning electron microscopy, energy dispersive spectroscopy, Fourier transform infrared spectroscopy, BET analysis and zeta potential measurements. The effects of CDC dosage, temperature, initial pH and agitation speed on the adsorption process were examined by using batch adsorption experiments. Moreover, the adsorption kinetics, thermodynamics, and isotherms were investigated. RESULTS: Adsorption and kinetic equilibrium data demonstrate that the adsorption of ibuprofen onto the CDC obeys the Langmuir isotherm model and the kinetics follow the pseudo-2nd order mechanism. The thermodynamic results reveal that ibuprofen adsorption is endothermic and spontaneous. The ibuprofen removal by CDC was mainly controlled by the electrostatic forces at high pH of the feed solution and by the dispersive interactions in acidic media. The ibuprofen removal is promoted at high temperature, high agitation speed and low pH. The highest adsorption capacity of ibuprofen onto the CDC was 367 mg/g at pH 3. Furthermore, the CDC efficiently removed ibuprofen from spiked treated sewage effluent. CONCLUSIONS: The obtained data indicate that the CDC provides a fast and efficient adsorptive removal of ibuprofen both from a model aqueous solution and treated sewage effluent.

Polysulfone Membranes Embedded with Halloysites Nanotubes: Preparation and Properties.

In the present study, nanocomposite ultrafiltration membranes were prepared by incorporating nanotubes clay halloysite (HNTs) into polysulfone (PSF) and PSF/polyvinylpyrrolidone (PVP) dope solutions followed by membrane casting using phase inversion method. Characterization of HNTs were conducted using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and thermogravimetric (TGA) analysis. The pore structure, morphology, hydrophilicity and mechanical properties of the composite membranes were characterized by using SEM, water contact angle (WCA) measurements, and dynamic mechanical analysis. It was shown that the incorporation of HNTs enhanced hydrophilicity and mechanical properties of the prepared PSF membranes. Compared to the pristine PSF membrane, results show that the total porosity and pore size of PSF/HNTs composite membranes increased when HNTs loadings were more than 0.5 wt % and 1.0 wt %, respectively. These findings correlate well with changes in water flux of the prepared membranes. It was observed that HNTs were homogenously dispersed within the PSF membrane matrix at HNTs content of 0.1 to 0.5 wt % and the PSF/HNTs membranes prepared by incorporating 0.2 wt % HNTs loading possess the optimal mechanical properties in terms of elastic modulus and yield stress. In the case of the PSF/PVP matrix, the optimal mechanical properties were obtained with 0.3 wt % of HNTs because PVP enhances the HNTs distribution. Results of bovine serum albumin (BSA) filtration tests indicated that PSF/0.2 wt % HNTs membrane exhibited high BSA rejection and notable anti-fouling properties.

Antibiofouling Performance by Polyethersulfone Membranes Cast with Oxidized Multiwalled Carbon Nanotubes and Arabic Gum.

Despite extensive research efforts focusing on tackling membrane biofouling, one of the biggest problems associated with membrane technology, there has been little headway in this area. This study presents novel polyethersulfone (PES) membranes synthesized via a phase inversion method at incremental loadings of functionalized oxidized multiwalled carbon nanotubes (OMWCNT) along with 1 wt. % arabic gum (AG). The synthesized OMWCNT were examined using scanning electron microscopy and transmission electron microscopy for morphological changes compared to the commercially obtained carbon nanotubes. Additionally energy-dispersive X-ray spectroscopy was carried out on the raw and OMWCNT materials, indicating an almost 2-fold increase in oxygen content in the latter sample. The cast PES/OMWCNT membranes were extensively characterized, and underwent a series of performance testing using bovine serum albumin solution for fouling tests and model Gram-positive (Bacillus subtilis) and Gram-negative (Escherichia coli) bacterial species for anti-biofouling experiments. Results indicated that the composite PES membranes, which incorporated the OMWCNT and AG, possessed significantly stronger hydrophilicity and negative surface charge as evidenced by water contact angle and zeta potential data, respectively, when compared to plain PES membranes. Furthermore atomic force microscopy analysis showed that the PES/OMWCNT membranes exhibited significantly lower surface roughness values. Together, these membrane surface features were held responsible for the anti-adhesive nature of the hybrid membranes seen during biofouling tests. Importantly, the prepared membranes were able to inhibit bacterial colonization upon incubation with both Gram-positive and Gram-negative bacterial suspensions. The PES/OMWCNT membranes also presented more resilient normalized flux values when compared to neat PES and commercial membrane samples during filtration of both bacterial suspensions and real treated sewage effluents. Taken together, the results of this study allude to OMWCNT and AG as promising additives, for incorporation into polymeric membranes to enhance biofouling resistance.

Performance of Acacia Gum as a Novel Additive in Thin Film Composite Polyamide RO Membranes.

Novel thin film composite (TFC) polyamide (PA) membranes blended with 0.01⁻0.2 wt.% of Acacia gum (AG) have been prepared using the interfacial polymerization technique. The properties of the prepared membranes were evaluated using contact angle, zeta potential measurements, Raman spectroscopy, scanning electron microscopy, and surface profilometer. It was found that the use of AG as an additive to TFC PA membranes increased the membrane's hydrophilicity (by 45%), surface charge (by 16%) as well as water flux (by 1.2-fold) compared with plain PA membrane. In addition, the prepared PA/AG membranes possessed reduced surface roughness (by 63%) and improved antifouling behavior while maintaining NaCl rejection above 96%. The TFC PA/AG membranes were tested with seawater collected from the Arabian Gulf and showed higher salt rejection and lower flux decline during filtration when compared to commercial membranes (GE Osmonics and Dow SW30HR). These findings indicate that AG can be used as an efficient additive to enhance the properties of TFC PA membranes.

Antibacterial Properties of Polysulfone Membranes Blended with Arabic Gum.

Polysulfone (PS) membranes blended with different loadings of arabic gum (AG) were synthesized using phase inversion method and the antibacterial properties of the synthesized membranes were tested using a number Gram-negative (Escherichia coli, Klebsiella pneumonia and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus) bacterial species. It was shown that AG addition to the dope polymer solutions essentially changed porous structure, hydrophilicity and zeta potential of the cast PS/AG membranes. These changes were due to the amphiphilic properties of AG macromolecules that contained negatively charged hydrophilic residues. A pronounced decrease in bacterial attachment was seen in the field emission scanning electron microscopy (FESEM) images for PS/AG membrane samples compared to both commercial (Microdyn-Nadir) and bare PS (without AG) membranes. AG loading dependent trend was observed where the prevention of bacterial colonization on the membrane surface was strongest at the highest (7 wt. %) AG loading in the casting solution. Possible mechanisms for the prevention of bacterial colonization were discussed. Significantly, the inhibition of bacterial attachment and growth on PS/AG membranes was observed for both Gram-positive and Gram-negative bacterial models, rendering these novel membranes with strong biofouling resistance attractive for water treatment applications.

Engineering the Surface and Mechanical Properties of Water Desalination Membranes Using Ultralong Carbon Nanotubes.

In this work, novel polysulphone (PS) porous membranes for water desalination, incorporated with commercial and produced carbon nanotubes (CNT), were fabricated and analyzed. It was demonstrated that changing the main characteristics of CNT (e.g., loading in the dope solutions, aspect ratio, and functionality) significantly affected the membrane properties and performance including porosity, water flux, and mechanical and surface properties. The water flux of the fabricated membranes increased considerably (up to 20 times) along with the increase in CNT loading. Conversely, yield stress and Young's modulus of the membranes dropped with the increase in the CNT loading mainly due to porosity increase. It was shown that the elongation at fracture for PS/0.25 wt. % CNT membrane was much higher than for pristine PS membrane due to enhanced compatibility of commercial CNTs with PS matrix. More pronounced effect on membrane's mechanical properties was observed due to compatibility of CNTs with PS matrix when compared to other factors (i.e., changes in the CNT aspect ratio). The water contact angle for PS membranes incorporated with commercial CNT sharply decreased from 73° to 53° (membrane hydrophilization) for membranes with 0.1 and 1.0 wt. % of CNTs, while for the same loading of produced CNTs the water contact angles for the membrane samples increased from 66° to 72°. The obtained results show that complex interplay of various factors such as: loading of CNT in the dope solutions, aspect ratio, and functionality of CNT. These features can be used to engineer membranes with desired properties and performance.

Removal of Cu(II) in water by polymer enhanced ultrafiltration: Influence of polymer nature and pH.

This study presents an efficient removal of Cu(II) in water using the polymer enhanced ultrafiltration (PEUF) method. Polymer of different molecular weight (MW) (polyethyleneimine (PEI), sodium lignosulfonates (SLS) and dextrans) were investigated to evaluate efficiency in removal of Cu(II) in water by the PEUF method. The decomposition of Cu(II)-polymer complex was also evaluated in order to reuse polymers. Cu(II) complexation depends on the MW of chelating polymer and the pH of feed solution. It was found that the Cu(II) rejection increased with the polymer dosage with high removal of Cu(II) when using PEI and SLS at a 10:20 (mg/mg) ratio ([Cu(II)]:[polymer]). It was found that the maximum chelating capacity was 15 mg of Cu(II) per 20 mg of PEI. The Cu(II)-PEI complex could be decomposed by acid addition and the polymer could be efficiently reused with multiple complexation-decomplexation cycles. A conceptual flow chart of the integrated process of efficient removal of Cu(II) by PEUF method is suggested.

Characterization and Separation Performance of a Novel Polyethersulfone Membrane Blended with Acacia Gum.

Novel polyethersulfone (PES) membranes blended with 0.1-3.0 wt. % of Acacia gum (AG) as a pore-former and antifouling agent were fabricated using phase inversion technique. The effect of AG on the pore-size, porosity, surface morphology, surface charge, hydrophilicity, and mechanical properties of PES/AG membranes was studied by scanning electron microscopy (SEM), Raman spectroscopy, contact angle and zeta potential measurements. The antifouling -properties of PES/AG membranes were evaluated using Escherichia coli bacteria and bovine serum albumine (BSA). The use of AG as an additive to PES membranes was found to increase the surface charge, hydrophilicity (by 20%), porosity (by 77%) and permeate flux (by about 130%). Moreover, PES/AG membranes demonstrated higher antifouling and tensile stress (by 31%) when compared to pure PES membranes. It was shown that the prepared PES/AG membranes efficiently removed lead ions from aqueous solutions. Both the sieving mechanism of the membrane and chelation of lead with AG macromolecules incorporated in the membrane matrix contributed to lead removal. The obtained results indicated that AG can be used as a novel pore-former, hydrophilizing and antifouling agent, as well as an enhancer to the mechanical and rejection properties of the PES membranes.