scholarly journals Preparation of Sodalite and Faujasite Clay Composite Membranes and Their Utilization in the Decontamination of Dye Effluents

Membranes ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 12
Author(s):  
Abderrazek El-kordy ◽  
Abdelaziz Elgamouz ◽  
El Mokhtar Lemdek ◽  
Najib Tijani ◽  
Salman S. Alharthi ◽  
...  
Keyword(s):  
Fine Particles ◽  
Water Flux ◽  
Nitrogen Adsorption ◽  
Composite Membranes ◽  
Sem Analysis ◽  
Size Exclusion ◽  
Point Of Zero Charge ◽  
Powder Metallurgy Method ◽  
Flow Loop ◽  
Methylene Orange

The present work describes the deposition of two zeolite films, sodalite and faujasite, by the hydrothermal method to tune the mesopores of clay support, which are prepared from a widely available clay depot from the central region of Morocco (Midelt). The clay supports were prepared by a powder metallurgy method from different granulometries with activated carbon as a porosity agent, using uniaxial compression followed by a sintering process. The 160 µm ≤ Φ ≤ 250 µm support showed the highest water flux compared to the supports made from smaller granulometries with a minimum water flux of 1405 L.m−2·h−1 after a working time of 2 h and 90 min. This support was chosen for the deposition of sodalite (SOM) and faujasite (FAM) zeolite membranes. The X-ray diffraction of sodalite and faujasite showed that they were well crystallized, and the obtained spectra corresponded well with the sought phases. Such findings were confirmed by the SEM analysis, which showed that SOM was crystalized as fine particles while the FAM micrographs showed the existence of crystals with an average size ranging from 0.53 µm to 1.8 µm with a bipyramidal shape and a square or Cubo octahedral base. Nitrogen adsorption analysis showed that the pore sizes of the supports got narrowed to 2.28 nm after deposition of sodalite and faujasite. The efficiencies of SOM and FAM membranes were evaluated by filtration tests of solutions containing methyl orange (MO) using a flow loop, which were developed for dead-end filtration. The retention of methylene orange (MO) followed the order: SOM > FAM > 160 µm ≤ Φ ≤ 250 µm clay support with 55%, 48% and 35%, respectively. Size exclusion was the predominant mechanism of filtration of MO through SOM, FAM, and the support. However, the charge repulsion between the surface of the membrane and the negatively charged MO have not been ruled out. The point of zero charge (pzc) of the clay support, SOM and FAM membrane were pHpzc = 9.4, pHpzc = 10.6, and pHpzc = 11.4, respectively. Filtrations of MO were carried out between pH = 5.5 and pH = 6.5, which indicated that the surface of the membranes was positively charged while MO was negatively charged. The interaction of MO with the membranes might have happened through its vertical geometry.

scholarly journals Microcrystalline Cellulose-Blended Polyethersulfone Membranes for Enhanced Water Permeability and Humic Acid Removal

Membranes ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 660
Author(s):  
Amirul Islah Nazri ◽  
Abdul Latif Ahmad ◽  
Mohd Hazwan Hussin
Keyword(s):  
Humic Acid ◽  
Pore Size ◽  
Composite Membrane ◽  
Microcrystalline Cellulose ◽  
Pure Water ◽  
Water Flux ◽  
Composite Membranes ◽  
Size Exclusion ◽  
Inversion Method ◽  
Water Contact

A novel polyethersulfone (PES)/microcrystalline cellulose (MCC) composite membrane for humic acid (HA) removal in water was fabricated using the phase inversion method by blending hydrophilic MCC with intrinsically hydrophobic PES in a lithium chloride/N,N-dimethylacetamide (LiCl/DMAc) co-solvent system. A rheological study indicated that the MCC-containing casting solutions exhibited a significant increase in viscosity, which directly influenced the composite membrane’s pore structure. Compared to the pristine PES membrane, the composite membranes have a larger surface pore size, elongated finger-like structure, and presence of sponge-like pores. The water contact angle and pure water flux of the composite membranes indicated an increase in hydrophilicity of the modified membranes. However, the permeability of the composite membranes started to decrease at 3 wt.% MCC and beyond. The natural organic matter removal experiments were performed using humic acid (HA) as the surface water pollutant. The hydrophobic HA rejection was significantly increased by the enhanced hydrophilic PES/MCC composite membrane via the hydrophobic–hydrophilic interaction and pore size exclusion. This study provides insight into the utilization of a low-cost and environmentally friendly additive to improve the hydrophilicity of PES membranes for efficient removal of HA in water.

scholarly journals Linking defects, hierarchical porosity generation and desalination performance in metal–organic frameworks

2018 ◽  
Vol 9 (14) ◽  
pp. 3508-3516 ◽  
Author(s):  
Weibin Liang ◽  
Lin Li ◽  
Jingwei Hou ◽  
Nicholas D. Shepherd ◽  
Thomas D. Bennett ◽  
...  
Keyword(s):  
Metal Organic Frameworks ◽  
Water Flux ◽  
Composite Membranes ◽  
High Salt ◽  
Salt Rejection ◽  
Hierarchical Porosity ◽  
Metal Organic

The composite membranes with defective metal–organic frameworks (MOFs) show a significant increase in water flux, without compromising the high salt rejection.

A study on the kinetics and thermal properties of polystyrene/diatomite nanocomposites prepared via in situ ATRP

2018 ◽  
Vol 33 (2) ◽  
pp. 180-197 ◽  
Author(s):  
Khezrollah Khezri ◽  
Yousef Fazli
Keyword(s):  
Molecular Weight ◽  
In Situ Polymerization ◽  
Structural Characteristics ◽  
Nitrogen Adsorption ◽  
Linear Increase ◽  
Size Exclusion ◽  
Scanning Calorimetry ◽  
Morphological Studies ◽  
Exclusion Chromatography

Pristine mesoporous diatomite was employed to prepare polystyrene/diatomite composites. Diatomite platelets were used for in situ polymerization of styrene by atom transfer radical polymerization to synthesize tailor-made polystyrene nanocomposites. X-Ray fluorescence spectrometer analysis and thermogravimetric analysis (TGA) were employed for evaluating some inherent properties of pristine diatomite platelets. Nitrogen adsorption/desorption isotherm is applied to examine surface area and structural characteristics of the diatomite platelets. Evaluation of pore size distribution and morphological studies were also performed by scanning and transmission electron microscopy. Conversion and molecular weight determinations were carried out using gas and size exclusion chromatography, respectively. Linear increase of ln ( M0/M) with time for all the samples shows that polymerization proceeds in a living manner. Addition of 3 wt% pristine mesoporous diatomite leads to an increase of conversion from 72% to 89%. Molecular weight of polystyrene chains increases from 11,326 g mol−1 to 14134 g mol−1 with the addition of 3 wt% pristine mesoporous diatomite; however, polydispersity index values increases from 1.13 to 1.38. Increasing thermal stability of the nanocomposites is demonstrated by TGA. Differential scanning calorimetry shows an increase in glass transition temperature from 81.9°C to 87.1°C by adding 3 wt% of mesoporous diatomite platelets.

scholarly journals EVALUATION OF BACTERIAL CELLULOSE-SODIUM ALGINATE FORWARD OSMOSIS MEMBRANE FOR WATER RECOVERY

2018 ◽  
Vol 80 (3-2) ◽  
Author(s):  
Ngan T. B. Dang ◽  
Liza B. Patacsil ◽  
Aileen H. Orbecido ◽  
Ramon Christian P. Eusebio ◽  
Arnel B. Beltran
Keyword(s):  
Contact Angle ◽  
Bacterial Cellulose ◽  
Sodium Alginate ◽  
Water Flux ◽  
Forward Osmosis ◽  
Composite Membranes ◽  
Membrane Thickness ◽  
Water Recovery ◽  
Sem Images ◽  
Salt Rejection

Water resources are very important to sustain life. However, these resources have been subjected to stress due to population growth, economic and industrial growth, pollution and climate change. With these, the recovery of water from sources such as wastewater, dirty water, floodwater and seawater is a sustainable alternative. The potential of recovering water from these sources could be done by utilizing forward osmosis, a membrane process that exploits the natural osmotic pressure gradient between solutions which requires low energy operation. This study evaluated the potential of forward osmosis (FO) composite membranes fabricated from bacterial cellulose (BC) and modified with sodium alginate. The membranes were evaluated for water flux and salt rejection. The effect of alginate concentrations and impregnation temperatures were evaluated using 0.6 M sodium chloride solution as feed and 2 M glucose solution as the draw solution. The membranes were characterized by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and Contact Angle Meter (CAM). The use of sodium alginate in BC membrane showed a thicker membrane (38.3 μm to 67.6 μm), denser structure (shown in the SEM images), and more hydrophilic (contact angle ranges from 28.39° to 32.97°) compared to the pristine BC membrane (thickness = 12.8 μm and contact angle = 66.13°). Furthermore, the alginate modification lowered the water flux of the BC membrane from 9.283 L/m2-h (LMH) to value ranging from 2.314 to 4.797 LMH but the improvement in salt rejection was prominent (up to 98.57%).

scholarly journals Chemically Cross-Linked Graphene Oxide as a Selective Layer on Electrospun Polyvinyl Alcohol Nanofiber Membrane for Nanofiltration Application

Nanomaterials ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 2867
Author(s):  
Myoung Jun Park ◽  
Grace M. Nisola ◽  
Dong Han Seo ◽  
Chen Wang ◽  
Sherub Phuntsho ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Polyvinyl Alcohol ◽  
Self Assembly ◽  
Water Flux ◽  
Composite Membranes ◽  
Cross Linking ◽  
Support Surface ◽  
Eosin Y ◽  
Selective Layer ◽  
Assembly Technique

Graphene oxide (GO) nanosheets were utilized as a selective layer on a highly porous polyvinyl alcohol (PVA) nanofiber support via a pressure-assisted self-assembly technique to synthesize composite nanofiltration membranes. The GO layer was rendered stable by cross-linking the nanosheets (GO-to-GO) and by linking them onto the support surface (GO-to-PVA) using glutaraldehyde (GA). The amounts of GO and GA deposited on the PVA substrate were varied to determine the optimum nanofiltration membrane both in terms of water flux and salt rejection performances. The successful GA cross-linking of GO interlayers and GO-PVA via acetalization was confirmed by FTIR and XPS analyses, which corroborated with other characterization results from contact angle and zeta potential measurements. Morphologies of the most effective membrane (CGOPVA-50) featured a defect-free GA cross-linked GO layer with a thickness of ~67 nm. The best solute rejections of the CGOPVA-50 membrane were 91.01% for Na2SO4 (20 mM), 98.12% for Eosin Y (10 mg/L), 76.92% for Methylene blue (10 mg/L), and 49.62% for NaCl (20 mM). These findings may provide one of the promising approaches in synthesizing mechanically stable GO-based thin-film composite membranes that are effective for solute separation via nanofiltration.

scholarly journals Cross-Linking With Diamine Monomers to Prepare Graphene Oxide Composite Membranes With Varying D-Spacing for Enhanced Desalination Properties

2021 ◽  
Vol 9 ◽  
Author(s):  
Hong Ju ◽  
Jinzhuo Duan ◽  
Haitong Lu ◽  
Weihui Xu
Keyword(s):  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
Water Flux ◽  
Covalent Bond ◽  
Composite Membranes ◽  
Rejection Rate ◽  
High Water ◽  
Cross Linking ◽  
Separation Performance ◽  
X Ray

As a new type of membrane material, graphene oxide (GO) can easily form sub-nanometer interlayer channels, which can effectively screen salt ions. The composite membrane and structure with a high water flux and good ion rejection rate were compared by the cross-linking of GO with three different diamine monomers: ethylenediamine (EDA), urea (UR), and p-phenylenediamine (PPD). X-ray photoelectron spectroscopy (XPS) results showed that unmodified GO mainly comprises π-π interactions and hydrogen bonds, but after crosslinking with diamine, both GO and mixed cellulose (MCE) membranes are chemically bonded to the diamine. The GO-UR/MCE membrane achieved a water flux similar to the original GO membrane, while the water flux of GO-PPD/MCE and GO-EDA/MCE dropped. X-ray diffraction results demonstrated that the covalent bond between GO and diamine can effectively inhibit the extension of d-spacing during the transition between dry and wet states. The separation performance of the GO-UR/MCE membrane was the best. GO-PPD/MCE had the largest contact angle and the worst hydrophilicity, but its water flux was still greater than GO-EDA/MCE. This result indicated that the introduction of different functional groups during the diamine monomer cross-linking of GO caused some changes in the performance structure of the membrane.

scholarly journals Polyvinylamine Membranes Containing Graphene-Based Nanofillers for Carbon Capture Applications

Membranes ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 119 ◽  
Author(s):  
Casadei ◽  
Venturi ◽  
Giacinti Baschetti ◽  
Giorgini ◽  
Maccaferri ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Carbon Capture ◽  
Mechanical Stability ◽  
Composite Membranes ◽  
Sem Analysis ◽  
Gas Permeation ◽  
Separation Performance ◽  
Low Grade ◽  
Atr Spectroscopy ◽  
Few Layer Graphene

In the present study, the separation performance of new self-standing polyvinylamine (PVAm) membranes loaded with few-layer graphene (G) and graphene oxide (GO) was evaluated, in view of their use in carbon capture applications. PVAm, provided by BASF as commercial product named LupaminTM, was purified obtaining PVAm films with two degrees of purification: Low Grade (PVAm-LG) and High Grade (PVAm-HG). These two-grade purified PVAm were loaded with 3 wt% of graphene and graphene oxide to improve mechanical stability: indeed, pristine tested materials proved to be brittle when dry, while highly susceptible to swelling in humid conditions. Purification performances were assessed through FTIR-ATR spectroscopy, DSC and TGA analysis, which were carried out to characterize the pristine polymer and its nanocomposites. In addition, the membranes′ fracture surfaces were observed through SEM analysis to evaluate the degree of dispersion. Water sorption and gas permeation tests were performed at 35 °C at different relative humidity (RH), ranging from 50% to 95%. Overall, composite membranes showed improved mechanical stability at high humidity, and higher glass transition temperature (Tg) with respect to neat PVAm. Ideal CO2/N2 selectivity up to 80 was measured, paired with a CO2 permeability of 70 Barrer. The membranes’ increased mechanical stability against swelling, even at high RH, without the need of any crosslinking, represents an interesting result in view of possible further development of new types of facilitated transport composite membranes.

scholarly journals The influences of polydopamine immersion time on characteristics and performance of polyvinylidene fluoride ultrafiltration membrane

2018 ◽  
Vol 197 ◽  
pp. 09007
Author(s):  
Syawaliah Syawaliah ◽  
Nasrul Arahman ◽  
Medyan Riza ◽  
Sri Mulyati
Keyword(s):  
Polyvinylidene Fluoride ◽  
Water Flux ◽  
Sem Analysis ◽  
Inversion Method ◽  
Asymmetric Structure ◽  
Pvdf Membrane ◽  
Before And After ◽  
Poly Ethylene ◽  
And Performance ◽  
Phase Inversion Method

The Polyvinylidene Fluoride (PVDF) membrane has been prepared by phase inversion method using N,N-dimethylacetamide (DMAc) as solvent and Poly Ethylene Glycol (PEG) as additive. The fabricated membrane was modified by Polydopamine (PDA) coating in concentration of 0.5 mg/ml and immersion times of 2 hours, 6 hours, and 24 hours. The characteristics and performance of the PVDF membranes before and after the modification are studied in this paper. The result of the water flux experiment showed that the PDA-coated PVDF membranes showcased a higher flux than that of pure PVDF membrane. Scanning Electron Microscopy (SEM) analysis confirmed that the membrane had an asymmetric structure consisting of two layers. There was no significant influence on the addition of PDA to the morphology of the pore matrix because the modification was done by surface coating. Fourier Transform Infrared Spectroscopy (FTIR) analysis showed that PDA was successfully introduced on the surface of PVDF membrane with the appearance of O-H from cathecol and N-H peaks at wavenumber range of 3300-3600 cm-1. Modification with PDA increased the mechanical strength of the membrane which affirmed by the results of the tensile and elongation at break evaluation.

Aqueous chemical grafting of modified-PEG onto maghemite nanoparticles: Influence of grafting conditions

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Claire-Hélène Brachais ◽  
Ling Hu ◽  
Diana Hach ◽  
Denis Chaumont ◽  
Aurélien Percheron ◽  
...  
Keyword(s):  
Covalent Bond ◽  
Nitrogen Adsorption ◽  
Average Diameter ◽  
Size Exclusion ◽  
Maghemite Nanoparticles ◽  
Chemical Grafting ◽  
Exclusion Chromatography ◽  
One Step ◽  
Aqueous Conditions ◽  
Xrd And Tem

AbstractThe synthesis of maghemite nanoparticles coated with triethoxysilanemonomethylether- PEG (Si-mPEG), is presented in aqueous conditions, by the “grafting to” process. This procedure is performed in one step, starting from anchored polymer and native nanoparticles. The maghemite nanoparticles obtained were first identified by XRD and the average diameter is about 10 nm according to the Nitrogen adsorption, XRD and TEM techniques. The nature of the catalysts (acetic acid, triethylamine, NH4OH and dibutyl-tin-dilaurate) used for the establishment of the covalent bond between the γ-Fe2O3 particles and the SimPEG, as well as the influence of the temperature and the reaction time, were evaluated on the grafting rate of the particles in water by TGA and FTIR techniques. Using the size exclusion chromatography, SEC technique, we showed that the monomethoxy-PEG was resistant to mild acidic up to strong basic conditions. The best ratio “time/amount of polymer” for the highest grafting rate was the use of tinbased organometallic compound (DBTL) at 80 °C during 48 h. In these conditions, a grafting rate of 54 % is achieved.

scholarly journals Fabrication and Assessment of ZnO Modified Polyethersulfone Membranes for Fouling Reduction of Bovine Serum Albumin

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Tshepo Duncan Dipheko ◽  
Kgabo Philemon Matabola ◽  
Kate Kotlhao ◽  
Richard M. Moutloali ◽  
Michael Klink
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Zno Nanoparticles ◽  
Bovine Serum ◽  
Pure Water ◽  
Water Flux ◽  
Composite Membranes ◽  
Optimal Performance ◽  
Fouling Resistance ◽  
Pure Water Flux

ZnO/PES composite membranes were fabricated by phase inversion method using DMAc as a solvent. The structure of ZnO was investigated using TEM, SEM, XRD, and TGA. TEM images of ZnO nanoparticles were well-defined, small, and spherically shaped with agglomerated nanoparticles particles of 50 nm. The SEM and XRD results were an indication that ZnO nanoparticles were present in the prepared ZnO/PES composites membranes. Contact angle measurements were used to investigate surface structures of the composite membranes. The amount of ZnO nanoparticles on PES membranes was varied to obtain the optimal performance of the composite membranes in terms of pure water flux, flux recovery, and fouling resistance using the protein bovine serum albumin (BSA) as a model organic foulant. The results showed that addition of ZnO to PES membranes improved the hydrophilicity, permeation, and fouling resistance properties of the membranes. Pure water flux increased from a low of 250 L/m2h for the neat membrane to a high of 410 L/m2h for the composite membranes. A high flux recovery of 80–94% was obtained for the composite membranes. The optimal performance of the composite membranes was obtained at 1.5 wt% of ZnO.

Sign in / Sign up

Export Citation Format

Share Document