Development of polysulfone-nanohybrid membranes using ZnO-GO composite for enhanced antifouling and antibacterial control

Zinc oxide nanoparticles were well-known for the enhanced antifouling and antibacterial properties which could be beneficial for membrane processes in desalination. The functionalization of ZnO onto graphene oxide nanoplates was targeted for better distribution. Both ZnO and ZnO-GO NPs were synthesized using sol-gel method. The nanoparticles characteristics were checked with XRD, TEM, and FESEM. The nanohybrid membranes were fabricated via wet phase inversion technique and embedded with various percentage of ZnO (1, 2, 3 wt%) and ZnO-GO (0.1, 0.3, 0.6 wt%) nanoparticles. All the membranes with nanoparticles incorporation exhibited improved membrane properties in comparison with the pristine PSF membrane. The best membrane performance was shown in membrane with 2 wt% of ZnO and 0.6 wt% of ZnO-GO. These two membranes presented significantly improved performance such as enhanced hydrophilicity, high permeability and porosity, improved humic acid rejection rate as well as good antifouling and antibacterial control. To an extent, the excellent antimicrobial ability of these nanohybrid membranes appeared as appropriate candidate to contribute or overcome bio-fouling issues in applications such as brackish water or seawater desalination. Hence, ZnO and ZnO-GO NPs were superb nanomaterials in the fabrication of PSF-nanohybrid membranes. The use of GO nanoplates allowed reduction of ZnO composition by up to 5 times while showing similar performances

Adsorption of Congo Red Dye Using Activated Carbon-Fe3O4 Composite

Activated Carbon-Fe3O4 composites were synthesized using co-precipitation method and used in batch experiments to adsorb Congo red dyes. The effect of adsorbent dosage, temperature and initial dye concentration was investigated. Increase in the adsorbent dosage resulted in the increase of dye adsorption capacity and the optimum dose was found to be 2 g/L. Increase in temperature had slightly negative impact on the adsorption which indicated the exhothermic nature of the adsorption process. Initial dye concentration also had significant impact on the adsorption process as the adsorption capacity of the AC- Fe3O4 adsorbents decreased with increase in dye concentrations. Finally, the obtained adsorption data were fitted to Langmuir adsorption isotherm and the maximum adsorption capacity of Activated Carbon-Fe3O4 adsorbent was found to be around 129.87 mg/g. Overall, the results suggested that synthesized AC- Fe3O4 composites exhibit significant potential to be used as an adsorbent for the removal of organic pollutants from aqueous solutions

Impact of combined oil-in-water emulsions and particulate suspensions on ceramic membrane fouling and permeability recovery

The application of crossflow ceramic microfiltration (CFCMF) to the removal of emulsified oil from a simple analogue of raw produced water (PW) arising from oil exploration has been studied. Outcomes relate to surfactant-stabilised oil-in-water (o/w) emulsions both as a discrete emulsion and in combination with a colloidal suspension of particulate solids (bentonite). The impact on both fouling during the filtration cycle and residual fouling of the ZrO2-TiO2 membrane, following aggressive caustic-acid chemical cleaning applied between six sequential 30-min filtration runs, was investigated. Results showed the addition of suspended solids to the o/w emulsion to be extremely deleterious to sustaining both the permeability and selectivity of the membrane. The addition of 1500 mg·L−1 of bentonite to a 10 vol.% emulsion resulted in a permeability decrease of 3.5–5 times over that recorded for the emulsion, and 8–36 times lower than that of the bentonite suspension. Oil passage through the microfiltration membrane (0.45 μm pore size) was concomitantly increased six-fold. Tests performed to assess the cleanability of the membrane demonstrated similar differences between the three feed liquids. The permanent fouling of the membrane by the combined emulsion/suspension reduced its permeability by a factor of 16 over that attained for the emulsion-fouled membrane, or 25 times less than the residual permeability of the membrane challenged with the suspended particles. Moreover, the residual permeability of the emulsion/suspension-fouled membrane was still in decline following the sixth run. The results emphasise the importance of considering possible particle-emulsion interactions in studying membrane filtration of PW analogues

Poly (amido amine) dendrimer based membranes for wastewater treatment - A critical review

Membrane based wastewater treatment technologies in which polymeric membranes are most commonly used have been extensively applied in water/wastewater treatment to help address the issue of water shortage through water/wastewater reclamation and reuse. However, polymeric membranes due to their hydrophobic nature are subject damage caused by accumulation of organic/inorganic fouling during filtration processes, which results in a number of issues such as low water flux and low pollutant rejection. Several strategies have been considered to address these challenges and effectively improve the membrane performances. Alteration of membrane properties strategy using suitable nanofillers such us poly (amido amine) or PAMAM has been largely studied. Herein, research efforts regarding the synthesis and properties of PAMAM along with the synthesis of PAMAM multifunctional nanocomposites were concisely reviewed for the first time. Membrane performance enhancement by incorporation of PAMAM were reviewed and discussed. Results and contributions achieved in the improvement of PAMAM incorporated membranes for the treatment of different types of wastewaters has been reviewed and summarized. Furthermore, perspectives on the current challenges and future research needs in the development and application of PAMAM incorporated polymeric membranes to benefit from the potentials that offer these promising new membrane nanofiller were discussed 2023 The Author(s)This research is made possible by graduate sponsorship research award (GSRA7-1-0510-20046) from Qatar National Research Fund (QNRF). The publication of this article was funded by Qatar National Library. The statements made herein are solely the responsibility of the authors Qatar National Library for funding the Open Access Publication.Scopu

Reaction kinetics of carbon dioxide with aqueous solutions of l-Arginine, Glycine & Sarcosine using the stopped flow technique

The use of amino acids as potential solvents for carbon dioxide (CO2) capture has been considered by a number of researchers. However, very little is known about the kinetics and mechanism of amino acids-CO2 reactions. In this work, we investigate the reactions of three amino acids (l-Arginine, Glycine and Sarcosine) with CO2 in aqueous media using stopped-flow conductivity technique. The experiments were performed at temperatures between 293 and 313K and amino acids concentrations were in the range of 0.05–0.2 molar. The overall rate constants (kov) was found to increase with increased amino acid concentration and solution temperature. Both zwitterion and termolecular mechanisms were used to model and interpret the data. However, the Zwitterion mechanism was found to be the preferred one. From the stopped-flow results at pH around 6, we found that neutral l-Arginine, Glycine and Sarcosine react with CO2(aq) with k(M−1s−1)=2.81×1010exp(−4482.9T(K)), k(M−1s−1)=3.29×1013exp(−8143.7T(K)) and k(M−1s−1)=3.90×1013exp(−7991.0T(K)) respectively. The corresponding activation energies are 37.28kJmol−1, 67.71kJmol−1 And 66.44kJmol−1 respectively. A comparison between the kinetics of the three amino acids showed that Arginine exhibits highest reaction rate with CO2 followed by Sarcosine and then Glycine. The technique and results obtained from this work can be used as strong tools in the development of efficient new solvents for the removal of CO2 from flue and industrial gases.This paper was made possible by an NPRP Grant # 7-1154-2-433 from the Qatar National Research Fund (a member of Qatar Foundation)

An Investigation of the Swelling Kinetics of Bentonite Systems Using Particle Size Analysis

Particles size distribution (PSD) is introduced as a tool for analysis of bentonite aggregation and swelling kinetics. Raw Ca-bentonite was purified using a combined wet sieving and sedimentation processes, followed by thermochemical treatment with Na 2 CO 3 to increase its swelling capacity. The detailed analysis of the PSD shows a strong correlation between the PSD and the swelling process. For the chemically treated raw bentonite, PSD revealed two different peaks representing unswelled and swelled particles along with some aggregates. The swelling is shown to be a kinetically controlled process that depends on time, temperature, and bentonite chemical composition. At the beginning of the chemical treatment, the effect of aggregates was more dominant; therefore, the viscosity did not increase much with particle size. However, the combined chemical and thermal treatment has enhanced the Na-activation process and boosted bentonite swelling. The rheological measurements have shown enhancement in the viscosity and confirmed the PSD findings. The same optimal treatment conditions are obtained from both rheological measurements and PSD analysis. A model is developed based on classical reaction rate kinetics and used to describe the conversion from unswelled to swelled particles. The PSD has a strong correlation with the physical properties of the suspension such as the viscosity. The swelling rate fits a second order model with a rate constant, k, in the range 0.002 to 0.124 h 1 and an activation energy, E, of 87 kJ/mol. PSD analysis together with the developed kinetic model are powerful tools for studying the swelling kinetics of bentonites.Scopu

Adsorption of organic water pollutants by clays and clay minerals composites: A comprehensive review

Clays and clay minerals are inexpensive, non-toxic, and naturally occurring minerals that have been utilized in water remediation as adsorbents. However, clays and clay minerals and those modified with heat, surfactants, acids, or organic-inorganic modifiers exhibit low adsorption capacity and re-generation ability towards organic water pollutants. The development of clays and clay minerals composites has gained considerable attention in recent years due to their enhanced adsorption capacity, ease of recovery from aqueous solution and improved physiochemical properties relative to raw and modified clays and clay minerals. This review aims to assess recent literature on clays and clay minerals composites including bentonite, montmorillonite and kaolinite intercalated with carbonaceous, metals, metal oxides, chitosan and polymeric materials and appraise their adsorption performance towards organic water pollutants. The review examines the effect of the composites' physicochemical properties on the adsorption performance and evaluates the adsorption mechanism as well as regeneration methods. The review also attempts to highlight the current progress in this area by assessing the outcomes of recently published articles and outline the research gaps for future research.This publication was made possible by an Award [GSRA6-2-0516-19029] from Qatar National Research Fund (a member of Qatar Foundation). The contents herein are solely the responsibility of the author[s]. Open access funding is provided by the Qatar National Library.Scopu

Novel Graphene-Zinc Iron Oxide Composite to Enhance Ultrafiltration Membrane Performance for Water Treatment and Desalination

The main target of membrane technologies such as the Ultrafiltration (UF), Nanofiltration (NF) and Reverse osmosis (RO) is to produce better filtration and separation of organic and inorganic substance from water as well as for longer life of the membrane. The phase inversion method is a well-known method to fabricate UF, NF and RO membranes for different application. The UF membrane is widely used in separation of macromolecules from solution as pretreatment stage with higher efficiency in hybrid process. The UF membrane made by pure polymer showed low flux, which affect on process performance of separation. The Polysulphone (PSF) is the most common polymer used in UF membrane which a hydrophobic material is making its surface prone to fouling due to adsorptive mechanism. This limitation of UF membranes have been solved by blended with nanoparticles incorporated membranes which showed significant enhancement on permeability, surface hydrophilicity, mechanical properties and other properties such as the selectivity. The main objective of this study to modify of UF membrane by blended with new composite nano-material for higher rejection of salt and organic substances. The graphene-zinc iron oxide composite as new nano-material was synthesized by sol gel method at low temperature of preparation. The composite was characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) to show the structure, morphology and particle size of nanoparticles. Thermal decomposition was determined using thermogravimetric-differential scanning calorimetry (TGDSC). The results showed that cubic system of zinc iron oxide nanoparticles with 8 nm of crystal size was obtained using XRD. The morphology using TEM showed zinc iron oxide composite graphene as layer of nanoparticles with size lower than 10 nm which confirmed the XRD results. The novel synthesized of zinc iron oxide nanoparticles embedded in graphene incorporated into polysulfone (PSF) with 0.5 wt. % loading which significant impact on the UF membrane properties was investigated. The effect of composite additive on membrane properties was investigated in terms of permeability, hydrophilicity (contact angle), zeta potential, porosity and pore size. However, the membrane cross section, surface, EDX and mapping were also analyzed using FESEM include EDX analyzer. This composite incorporated PSF showed significant improvement in terms of surface hydrophilicity with reduction of about 25% (reduce contact angle from 82 to 62). This improvement confirms by increasing the zeta potential values and surface negatively charge of blended PSF with composite compared to pure PSF membrane. The permeability results showed that significant increased more than two times compared to pure PSF membrane. The phenomenon of permeability increasing was attributed to increase of porosity of blended membrane which becomes lower resistance of water permeation. Generally, the rate of pore production has been reported directly affected by rate of solvent and non-solvent exchange in phase inversion process. However, higher rejections of organic substances such as the dyes and humic acid as well as the salt such as Sodium sulfate (Na2SO4) were maintained using UF at low pressure. This enhancement affects on time and load of process especially when hybrid with Nanofiltration (NF) which can increase of membrane life and reduce of overall process cost. The results of this study will have bigger impact in the future for different application including for water treatment and desalination.qscienc

Mechanical Behavior of a Novel Nanocomposite Polysulphone - Carbon Nanotubes Membrane for Water Treatment

Nowadays, global fresh water shortage is becoming the most serious problem affecting the economic and social development. Water treatment including seawater desalination and wastewater treatment is the main technology for producing fresh water. Membrane technology is favored over other approaches for water treatment due to its promising high efficiency, ease of operation, chemicals free, energy and space saving. Membrane filtration for water treatment has increased significantly in the past few decades with the enhanced membrane quality and decreased membrane costs. In addition to high permeate flux and high contaminant rejection, membranes for water treatment require good mechanical durability and good chemical and fouling resistances. Thus, investigation of the mechanical behavior of water treatment membranes with underlying deformation mechanisms is critical not only for membrane structure design but also for their reliability and lifetime prediction. Compared to ceramic and metallic membranes, polymer membranes with smaller pore size and higher efficiency for particle removal are widely used in seawater desalination with a high applied pressure. However, polymer membranes are mechanically weaker and have lower thermal and chemical stability compared to inorganic membranes. Blending of polymers with inorganic fillers is an effective method to introduce advanced properties to polymer based membranes to meet the requirements of many practical applications. The reinforced polymeric membranes with inorganic fillers can provide desirable mechanical strength as well as mechanical stability. Carbon nanotubes (CNTs) have received considerable attention from academic and industries over the last twenty years. In addition to their excellent electrical and thermal properties, CNTs exhibit outstanding mechanical characteristics due to its instinct mechanical strength and high aspect ratio. For the application of water treatment membranes, CNTs could be the excellent channels for water to go through and therefore, CNTs have proven to be excellent fillers in polymer membranes improving the permeability and rejection properties. In literature, it is reported that the mechanical strength of the polymer membranes was improved with the embedding of CNTs due to reinforcement effect of the more rigid CNTs. The mechanical responses of polymer_CNTs composites depended on the interfacial adhesion between the CNTs and the membrane-based polymer as well as the dispersion and distribution of the CNTs within the polymer matrix. In this study, a vertical chemical vapor deposition reactor was designed in order to synthesize CNTs of high aspect ratio using continues injection atomization. Bundles of high purity (99%) and high quality CNTs were produced by this system. The produced CNTs had diameters ranging from 20 to 50 nm and lengths ranging from 300 to 500 micron (corresponded aspect ratios ranging from 6000 to 25000). A novel polysulphone (PSF) based nanocomposite membrane incorporated with the produced high aspect ratio CNTs was then casted via phase inversion method, at a wide range of CNTs loading (0-5 wt. %), in polysulphone-dimethylformamide solutions using the Philos casting system. The poly(vinylpyrrolidone) was used as pore-forming additive. To demonstrate the effect of nanocomposite morphology on the mechanical behavior of the prepared membranes, a set of control samples consisted of PSF membranes embedded with commercial CNTs at the same CNTs loading, were casted at the same conditions. The commercial CNTs had a lengths of 1 ?m to 10 ?m and outer diameters of 10 nm to 20 nm (corresponded aspect ratios ranging from 50 to 1000), with purity >95% and BET surface area of 156 m2/g. The effects of CNTs content and aspect ratio on morphological, water transport and mechanical properties of the prepared PSF-based porous membranes were investigated. The surface and cross-section morphologies of PSF/CNTs porous membranes were examined using scanning electron microscopy (SEM). The orientation, dispersion and distribution of CNTs within polymer membranes were evaluated for the membrane samples with different CNTs content and CNTs aspect ratio. The average membrane pore size was evaluated by using SEM image analysis software. Uniaxial tensile behavior of the membranes was characterized by means of a universal material testing machine under different testing conditions. Wet specimens were carefully cut from the casted membranes by using a razor blade. Elastic, plastic and failure behaviors of the membranes are analyzed with the impacts of CNTs content and aspect ratio. The macroscopic mechanical behaviors of the membranes are correlated with their strain induced microstructure evolution by using SEM. In this, pore shape evolution, pore and CNTs orientations, neighboring pore interaction, interface between the CNTs and PSF matrix and the failure behavior of the deformed porous membranes were analyzed. The macroscopic stress-strain responses of the membranes were correlated with the microstructure of the studied nanocomposites membranes to provide a better understanding of materials' processing-microstructure-properties relationship.qscienc

Adsorption of 4-Nitrophenol onto Iron Oxide Bentonite Nanocomposite: Process Optimization, Kinetics, Isotherms and Mechanism

Despite its importance in chemical industry, 4-Nitrophenol (4-NP) is a persistent organic pollutant that has serious effects on the ecosystem. In the present study, Box–Behnken design in response surface methodology was used to optimize the adsorption process parameters for the maximum 4-NP removal at 30 ℃ using Fe3O4/Bt NC. The regression model results suggested that the optimum adsorbent dosage, initial concentration, pH and contact time were 0.3182 g, 85 mg/L, 11 and 137.2 min, respectively. The regression model showed an optimum removal of 100%, while 99.5% removal was obtained from batch experiments at the optimum conditions suggested by the regression model, which confirm the model validity. The adsorption data best fitted to Freundlich isotherm model and Pseudo second-order kinetic model suggesting the existence of physical and chemical interaction between the fabricated composite and 4-NP. FTIR analysis suggested that the adsorption mechanism included an electrostatic attraction and the formation of new chemical bonds. Obtained results suggest that Fe3O4/Bt NC can be an effective adsorbent for complete 4-NP removal at the indicated optimum conditions.This research was made possible by an NPRP Grant # 10-0127-170270 from the Qatar National Research Fund (a member of Qatar Foundation). The statements made herein are solely the responsibility of the authors. The author Dina Ewis acknowledged the financial support of QNRF through the Graduate Sponsorship Research Award (GSRA) number GSRA#6-2-0516-19029.Scopu