Synergistic effect of GO/ZnO loading on the performance of cellulose acetate/chitosan blended reverse osmosis membranes for NOM rejection.

Declining freshwater resources along with their pollution are threatening the life existence on earth. To meet the freshwater demand, one of the most appropriate and possible ways which has been adopted all over the world is to reuse wastewater by removing its impurities. Among many water pollutants, natural organic matter (NOM) is found to be responsible as major precursor for the formation of other pollutants. Removal of NOM from wastewater is being done by using membrane filtration systems incorporated with certain nanofillers to increase membranes efficiency and permeability. In this study, novel nanocomposite reverse osmosis (RO) membranes were prepared using cellulose acetate and chitosan in N,N-Dimethyl formamide. Graphene oxide (GO) nanosheets and zinc oxide (ZnO) in different concentration were loaded to modify the membranes for tuning their RO performance. The confirmation of the functional groups is demonstrated by Fourier transform infrared spectroscopy which revealed the specific peaks indicating the formation of the nano-composite membranes. The surface morphology was studied by scanning electronic microscopy which shows a gradual transformation of the membrane surface from voids-free to macro-voids filled surface up to threshold concentration of GO and ZnO. The thermal properties of GO based membranes were analyzed using thermogravimetric analysis and differential scanning calorimetry. The uniform interaction of the GO and ZnO with polymers induced the remarkable thermal properties of the synthesized membranes. Permeate flux and contact angle measurements were considered to estimate their water content (96%) capacity and NOM rejection (96%) using 0.1 ppm humic acid solution. The permeate flux, NOM rejection and the water content changed directly with GO and inversely with ZnO wt% in the membranes up to GO5 (GO:0.14: ZnO:0.03) whereas the contact angle exhibited the inverse relationship with GO and ZnO concentration in casting solution of the synthesized membranes. Hence it can be concluded that prepared RO membranes are suitable for NOM rejection and recommended for water treatment.

Novel antibacterial polyurethane and cellulose acetate mixed matrix membrane modified with functionalized TiO2 nanoparticles for water treatment applications.

Bacterial contamination is one of the leading causes of water pollution. Antibacterial polyurethane/cellulose acetate membranes modified by functionalized TiO2 nanoparticles were processed and studied. TiO2 nanoparticles were prepared and ultraviolet (UV) irradiated to activate their photocatalytic activity against Escherichia coli (E. Coil) and Methicillin-resistant Staphylococcus aureus (MRSA) bacteria. Functionalized TiO2 nanoparticles were incorporated in flat-sheet mixed matrix membranes (MMMs). These membranes were characterized for their different properties such as morphology, thermal stability, mechanical strength, surface wettability, water retention, salt rejection, water flux, and their antibacterial performance against E. Coil and MRSA was also tested. The activity of nanoparticles against MRSA and E. coli was analyzed using three different concentrations, 0.5 wt%, 1.0 wt% and 1.5 wt% of nanoparticles and 0.5 wt% of TiO2 nanoparticles showed maximum growth of bacteria. The maximum inhibition was observed in membranes with maximum nanoparticles when compared with other membranes. All these characteristics were strongly affected by increasing the concentration of TiO2 nanoparticles in the prepared membranes and the duration of their UV exposure. Hence, it was proved from this analysis that these TiO2 modified membranes exhibit substantial antibacterial properties. The results are supporting the utilization of these materials for water purification purposes.

Alkyl Silica Hybrid Nanowire Assembly in Improved Superhydrophobic Membranes for RO Filtration.

Alkyl silica membranes and wires were synthesized by a sol-gel method, which has the capacity to control the size of the particles or membranes by controlling the reactions. Trimethoxyoctylsilane (C8TMOS) was used as a chemical surfactant; poly(vinylpyrrolidone) (PVP) as an emulsifier, dissolved in butanol for emulsion; and tetraethylorthosilicate (TEOS) as a precursor and a source of silica. An assembly of silica wires was fabricated on glass and cotton substrates by the dip-coating technique. Porous membranes and silica wires were observed using scanning electron microscopy (SEM) images. The contact angles of all of the samples were in the range of 140-154° as measured by ImageJ software, which confirmed the hydrophobic nature of the samples. The contact angle was increased by increasing the amount of the surfactant. Phase changes of silica wires and membranes were investigated by thermogravimetric analysis. Chemical bonds of the sample were studied using Fourier transform infrared (FTIR) spectroscopy. The band gap of silica nanowires was measured to be 3.8-3.4 eV using the UV-visible spectrum and decreased as compared to that of bulk silica. These silica-based porous membranes with enhanced transport properties can be used in filtration and separation techniques. This fabricated hybrid silica membrane showed ∼96% salt rejection within a permeation flux of 3.04 L/m2 h.

Sodium alginate blended membrane with polyurethane: Desalination performance and antimicrobial activity evaluation.

A series of polymeric membranes were synthesized by blending polyurethane with sodium alginate (0.2, 0.4, 0.6, 0.8 and 1.0%). The structural, morphological and thermal properties of the membranes were examined by FTIR, SEM, AFM and TGA, respectively. Performance evaluation (salt rejection and flux) was assessed through reverse osmosis technique (RO). The FTIR spectra of membranes confirmed extensive hydrogen bonding (3350 cm-1). The SEM and AFM analyses supported a progressively rising surface roughness of blended membranes. The hydrophilicity, crosslinking density and thermal stability of the membranes were improved with an increase in alginate content. The capability of salt (NaCl and MgCl2) rejection was improved with alginate up to 0.8%. In addition, the rejection of divalent ions was better than monovalent ions (94 ± 0.96% for NaCl and 98 ± 0.98% for MgCl2). The blended membranes ascertained an effective chlorine resistivity. The antibacterial activity was also promising, which enhanced with the alginate content in the membrane. The sodium alginate blended membrane with polyurethane proved to be an efficient approach to develop the blended membranes with tunable properties for water desalination.

Effect of Varying Amount of Polyethylene Glycol (PEG-600) and 3-Aminopropyltriethoxysilane on the Properties of Chitosan based Reverse Osmosis Membranes.

Chitosan and polyethylene glycol (PEG-600) membranes were synthesized and crosslinked with 3-aminopropyltriethoxysilane (APTES). The main purpose of this research work is to synthesize RO membranes which can be used to provide desalinated water for drinking, industrial and agricultural purposes. Hydrogen bonding between chitosan and PEG was confirmed by displacement of the hydroxyl absorption peak at 3237 cm-1 in pure chitosan to lower values in crosslinked membranes by using FTIR. Dynamic mechanical analysis revealed that PEG lowers Tg of the modified membranes vs. pure chitosan from 128.5 °C in control to 120 °C in CS-PEG5. SEM results highlighted porous and anisotropic structure of crosslinked membranes. As the amount of PEG was increased, hydrophilicity of membranes was increased and water absorption increased up to a maximum of 67.34%. Permeation data showed that flux and salt rejection value of the modified membranes was increased up to a maximum of 80% and 40.4%, respectively. Modified films have antibacterial properties against Escherichia coli as compared to control membranes.

Novel Maleic Acid, Crosslinked, Nanofibrous Chitosan/Poly (Vinylpyrrolidone) Membranes for Reverse Osmosis Desalination.

Fresh and clean water is consistently depleting and becoming a serious problem with rapid increases in population, so seawater desalination technology has captured global attention. For an efficient desalination process, this work proposes a novel, nanofibrous, thin-film composite membrane (NF-TFC) based on the deposition of the nanofibrous active layer of a blend of chitosan (CS) and poly (vinylpyrrolidone) (PVP) crosslinked with maleic acid on a 3-triethoxysilylpropylamine functionalized cellulose acetate substrate. FTIR analysis demonstrated the development of chemical and physical interactions and confirmed the incorporation of functional groups present in the NF-TFC. Scanning electron microscopy (SEM) micrographs depict the fibrous structure of the active layers. The reverse osmosis (RO) desalination characteristics of NF-TFC membranes are elevated by increasing the concentration of the crosslinker in a CS/PVP blend. Cellulose acetate (CA)-S4 attained an optimal salt rejection of 98.3% and permeation flux of 42.9 L/m2h, suggesting that the NF-TFC membranes could be favorable for seawater desalination.

A Review of Biodegradable Natural Polymer-Based Nanoparticles for Drug Delivery Applications.

Biodegradable natural polymers have been investigated extensively as the best choice for encapsulation and delivery of drugs. The research has attracted remarkable attention in the pharmaceutical industry. The shortcomings of conventional dosage systems, along with modified and targeted drug delivery methods, are addressed by using polymers with improved bioavailability, biocompatibility, and lower toxicity. Therefore, nanomedicines are now considered to be an innovative type of medication. This review critically examines the use of natural biodegradable polymers and their drug delivery systems for local or targeted and controlled/sustained drug release against fatal diseases.

Designing of biocompatible and biodegradable chitosan based crosslinked hydrogel for in vitro release of encapsulated povidone-iodine: A clinical translation.

Controlled drug delivery is a prime stratagem for minimizing both the frequency of therapeutic administration as well as systematic side effects with high drug content. One of the extensively studied approaches for controlling medicament delivery is the encapsulation of drug within polymer chains which sluggish the release on the basis of its crosslinked network. Recent advances in biomedical field have led to the fabrication of chitosan (CS) based biocompatible and biodegradable hydrogels for controlled delivery of encapsulated drug. In this study, CS-PVP based hydrogels are fabricated by varying the concentration of 3-glycidyloxypropyl trimethoxysilane (GPTMS) via solution casting technique. Swelling indices of prepared hydrogel samples were determined in different media including distilled water, different pH and electrolyte solutions. FTIR, TGA and WAXRD are conducted to evaluate the structural, thermal and crystalline properties of prepared hydrogels, respectively. Porosity (71%), hydrophilicity (55°) and mechanical properties (97.56 MPa of UTS and 85.23% E%) were investigated for the fabricated samples. Extensively in vitro biodegradation, antimicrobial performance and cytotoxicity were evaluated for these hydrogels. The drug release analysis was carried out to examine the release response of encapsulated iodopovidone at physiological conditions. These results tender a strategy for the design of structural hydrogel with different crosslinking mechanism like physical and covalent interactions. These insights obviate the demand for encapsulation and offer promising and translatable strategies for more effective release of drugs.

Novel N-p-carboxy benzyl chitosan/poly (vinyl alcohol/functionalized zeolite mixed matrix membranes for DMFC applications.

The novel N-p-carboxy benzyl chitosan (CBC)/ poly (vinyl alcohol) (PVA) based mixed matrix membranes (MMMs) filled with surface-modified zeolite have been prepared using the dissolution casting technique. The applicability of prepared MMMs for direct methanol fuel cell (DMFC) was investigated in terms of water uptake, methanol permeation, and proton conductivity by changing filler content (10-50 wt. %). The zeolite was modified by silane coupling agent, 3-mercaptopropyltrimethoxysilane (MPTMS). The resultant modified zeolite (MZ) was incorporated into CBC/PVA blend to obtain mixed matrix PEMs. The functional group, structural properties, morphological and topographical investigation of MMMs were examined using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Scanning electron microscopy (SEM) respectively. The prepared MMMs exhibited a remarkable decrease in methanol permeability of 2.3 × 10-7  cm2/s with C-CPMZ50. The maximum value of proton conductivity of 0.0527 Scm-1, was shown by C-CMPZ10. The prepared PEMs also displayed good stability during long term operating time.

Development of inter-polymeric complex of anionic polysaccharides, alginate/k-carrageenan bio-platform for burn dressing.

A novel approach in fabricating anionic inter-polymeric complex polysaccharide bio-platform with enhanced mechanical, structural and chemical properties for burn wound dressings. This approach implies a facile, insitu method to design soft nano-floral inter-polymeric complexes. In particular, sodium alginate (SA) and kappa-carrageenan (k-Ca) treated silver salt results in nano-floral inter-polymeric complex with self-stability. SEM images depict nano-floral complexes with surface plasmon resonance at 412-425 nm. These were resistant towards Staphylococcus aureus and Escherichia coli bacterium. These nano-floral complexes were then subjected to wound closure diameter and histological analysis. Designed polymeric complexes enhanced exudate absorption thus promotes effective proliferation, the appearance of compact fibrous arrangement and hair follicles i.e. facilitates healing for second-degree burn wound.

Transparent Hydrophobic Hybrid Silica Films by Green and Chemical Surfactants.

Monodispersed and transparent hybrid silica wires were synthesized by the sol-gel method using the chemical surfactant trimethoxyoctylsilane (C8TMOS or C11H26O3Si) and, for the first time, by green surfactants (Nelumbo nucifera/lotus leaf extract). The purpose was to introduce a less toxic, cost-effective, and one-step easy approach to get superhydrophobic silica films. Each of the surfactants was used at two different concentrations to investigate hydrophobicity of the films. Assembly of silica wires was obtained by dip-coating and vacuum filtration methods on glass and cellulose acetate filter paper as substrates, respectively. The water contact angle (CA) up to 154° was measured for hybrid silica films on filter paper, which revealed their superhydrophobicity as compared to hydrophobic behavior of those films coated on a glass substrate with CA up to 135°. Chemical, optical, and structural properties of prepared films were characterized by Fourier transform infrared spectroscopy, UV-vis spectroscopy, scanning electron microscopy, thermogravimetry, and differential scanning calorimetry. The hybrid silica wires prepared displayed good transparency, low surface energy, and superhydrophobicity. These silica assemblies can create outstanding and multifunctional structures with superhydrophobic coatings for waterproof electronic devices, military uniforms, self-cleaning surfaces, etc.

Fractionation of direct dyes using modified vapor grown carbon nanofibers and zirconia in cellulose acetate blend membranes.

In the textile industry, membrane technology has been widely employed for the exclusion of direct dyes. In this research paper, firstly vapor grown carbon nanofibers (VGCNFs) were functionalized with carboxylates group via piranha oxidation, and then series of CA/PEO-PPO-PEO triblock copolymers were prepared by blending with varying weight percentages of modified VGCNFs and Zirconia (ZrO2). The structural morphologies of membranes were visualized by scanning electron microscope (SEM), atomic force microscopy (AFM) and transmission electron microscopy (TEM), which exhibits the dispersity of dual fillers in polymer matrix thus improving the microstructure of resultant membranes. The experimental data indicates that the modified VGCNF and ZrO2 nanoparticles were shown increase hydrophilic character. The direct dyes rejection were successfully after filler addition, which were 96% (for Direct Red), 99% (for Direct Blue) and 93% (for Direct Orange). The membranes showed a better antifouling property even after several washing cycles along with improved biofouling property, both of these properties showed a better membrane life. As an outcome, this research could have been a great potential to be used to treat dyes in textile industry.

Cellulaose acetate based thin film nanocomposite reverse osmosis membrane incorporated with TiO2 nanoparticles for improved performance.

In this work, cellulose acetate (CA) based thin film nanocomposite reverse osmosis (RO) membranes were fabricated using dissolution casting method by optimizing the CA/polyethylene glycol (CA/PEG-400) ratios for improved RO performance. The selectivity of optimized membrane was further enhanced by incorporating TiO2 (0-25 wt.%) nanoparticles. Fourier transform infrared spectroscopy (FTIR), thermogravimetric analyzer (TGA), scanning electron microscopy (SEM) and X-ray diffraction (XRD) were conducted to characterize control and modified membranes for the analysis of functional groups, thermal properties, morphology and structural investigation respectively. CP-2 of CA/PEG-400 (80/20) was selected for further modification with TiO2 nanoparticles. The maximum salt rejection (95.4%) was observed for the membrane having 15% TiO2 nanoparticles. Further escalation of TiO2 concentration resulted in the agglomeration of nanoparticles which subsequently decreased the permeation flux. The test results demonstrated that the modified membranes had higher salt rejection and chlorine resistance, lower degradation profile, successful inhibition of Escherichia coli growth and facilitating permeation flux compared to the control membrane.

The effect of Nanocrystalline cellulose/Gum Arabic conjugates in crosslinked membrane for antibacterial, chlorine resistance and boron removal performance.

In this work, we developed hybrid membranes integrated with Nanocrystalline cellulose (NCC)/Gum Arabic (GuA) conjugates using crosslinked Poly (vinyl alcohol) (PVA) as a matrix phase with the addition of PEO-PPO-PEO block copolymer that insured pore formation. At first, the NCC was prepared from microcrystalline cellulose via acid hydrolysis process. The performance property of hybrid NCC/GuA was measured using boron removal. The results showed that the rejection capability enhanced as compared to the control membranes, especially at 0.1wt% of NCC the selectivity is up to 92.4% with the flux rate of 21.3L/m2.h. Moreover, the GuA in NCC/GuA conjugate significantly enhances the antibacterial activity by hindering the bacterial attachment to the surface as both of them carry the negative charge. Also by providing the active sites responsible for hydrogen bonding thus enhancing the hydrophilic character resulted in increased permeation flux rate. Therefore, the NCC/GuA conjugated membranes have great potentials for boron removal.

Decoration of open pore network in Polyvinylidene fluoride/MWCNTs with chitosan for the removal of reactive orange 16 dye.

Inspired by the hydrophilic, biocompatible, adsorbent properties of chitosan. A simple, adaptable, green synthesis method was developed to prepare a thin film composite membranes using chitosan as a pore decorating material for the removal of anionic dye-Reactive orange 16 (RO-16). The hydrophilic chitosan was used to fill up the porous hydrophobic PVDF substrate, modified by MWCNTs. The dye rejection was carried out through the formation of a strong electrostatic interaction between the cationic group of chitosan surface and the anionic group of RO-16 dye. The dye molecules accumulate on the chitosan surface, thus promoting the higher retention rate. The TFC membranes were evaluated using dead filtration plant. It is found that the modified membranes showed RO-16 rejection up to 91% with optimum permeation flux of 170kgm-2h-1. Furthermore, the presence of chitosan on MWCNT/PVDF substrate provides a hydrophilic character thus decreasing the active sites available for foulant attachment which is confirmed by the fouling study. The CTAB foulant showed an increase in flux rate even after physical flushing. The modification procedure is performed under mild conditions, thus it is helpful to fabricate TFC membrane at a commercial scale.

Novel reverse osmosis membranes composed of modified PVA/Gum Arabic conjugates: Biofouling mitigation and chlorine resistance enhancement.

A novel crosslinked Poly (vinyl alcohol) (PVA) reverse osmosis (RO) thin film membrane conjugated with Gum Arabic (GA) with superb performance and features was synthesized for water desalination. RO membrane desalination parameters, such as hydrophilicity, surface roughness, water permeability, salt rejection, Chlorine resistance and biofouling resistance were evaluated using a dead end RO filtration unit. The incorporation of Pluronic F127 and the conjugation of Gum Arabic improved the overall RO performance of the membranes. This study has shown that the membrane PVA-GA-5 that contains 0.9wt% Gum Arabic provided excellent permeation, salt rejection, Chlorine and biofouling resistance and mechanical strength. The most remarkable result to arise from this research is that the overall RO performance enhancement has been achieved while utilizing PVA/Gum Arabic as a separation layer without the use of a substrate, which eliminates negative effects associated with the use of a substrate like internal concentration polarization.

Fabrication and performance characteristics of tough hydrogel scaffolds based on biocompatible polymers.

Novel silane crosslinked tough hydrogel scaffolds were prepared using chitosan (CS) and polyvinyl alcohol (PVA) to give network structure and scaffolds properties. The influence of crosslinking and PVA concentration on scaffolds were studied. Fourier transform infrared spectroscopy (FTIR) spectroscopy confirmed the presence of incorporated components. Tensile strength (TS) and fracture strain analysis of scaffolds were detected owing to the mutual effect of chemically and physically crosslinked network. Tough hydrogel scaffolds having 90% CS and 10% PVA exhibited TS of 49.18MPa and 10.15% elongation at break. The contact angle is less than 90° exhibited the hydrophilic nature of the scaffold. X-ray diffraction analysis (XRD) indicated the characteristics peaks fitting to CS and PVA and increase in the crystallinity of scaffolds. Cytotoxicity of scaffolds with different human fibroblast cell lines (F121, F192 and F84) for indirect method and human dermal fibroblast cell lines (F121) for direct method was evaluated. This indicated that these biomaterials were non-toxic, viable to the used cell lines, helpful in the growth of these cells and did not discharge toxic material damaging to the living cells.

Self-sterilized composite membranes of cellulose acetate/polyethylene glycol for water desalination.

Cellulose acetate/Polyethylene glycol-600 composite membranes were fabricated by two step phase inversion procedure and modified by in-situ reduction of silver nitrate. FTIR spectra demonstrated the existence of functional groups for bonding of silver with oxygen at 370cm(-1), 535cm(-1). The XRD diffractogram indicates characteristic peaks at 2θ values of 38.10°, 44.30°, 64.40°, and 77.30° which confirm the successful incorporation of silver within matrix of composite membranes. The morphology of composite membranes with appearances of spongy voids was exemplified from the scanning electron microscope. The atomic force microscopy was used to determine the increase in the surface roughness of the membranes. The increase in hydrophilicity, measured through contact angle, is rendered to the embedment of silver. The modification of membranes increased the flux from 0.80 to 0.95L/hr.m(2). The resulting membranes have outstanding ability to fight against gram negative Escherichia Coli and Bacillus Sabtilus. The novel cellulose acetate/polyethylene glycol membranes customized with silver have paved the path for evolution of axenic membranes.

Novel green nano composites films fabricated by indigenously synthesized graphene oxide and chitosan.

Graphene oxide (GO) was indigenously synthesized from graphite using standard Hummers method. Chitosan-graphene oxide green composite films were fabricated by mixing aqueous solution of chitosan and GO using dilute acetic acid as a solvent for chitosan. Chitosan of different viscosity and calculated molecular weight was used keeping amount of GO constant in each composite film. The structural properties, thermal stability and mechanical properties of the composite films were investigated using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and tensile test. FTIR studies revealed the successful synthesis of GO from graphite powder and it was confirmed that homogenous blending of chitosan and GO was promising due to oxygenated functional groups on the surface of GO. XRD indicated effective conversion of graphite to GO as its strong peak observed at 11.06° as compared to pristine graphite which appeared at 26°. Moreover, mechanical analysis confirmed the effect of molecular weight on the mechanical properties of chitosan-GO composites showing that higher molecular weight chitosan composite (GOCC-1000) showed best strength (higher than 3GPa) compared to other composite films. Thermal stability of GOCC-1000 was enhanced for which residual content increased up to 56% as compared to the thermal stability of GOCC-200 whose residue was restricted to only 24%. The morphological analysis of the composites sheets by SEM was smooth having dense structure and showed excellent interaction, miscibility, compatibility and dispersion of GO with chitosan. The prepared composite films find their applications as biomaterials in different biomedical fields.

Conjugation of silica nanoparticles with cellulose acetate/polyethylene glycol 300 membrane for reverse osmosis using MgSO4 solution.

Thermally-induced phase separation (TIPS) method was used to synthesize polymer matrix (PM) membranes for reverse osmosis from cellulose acetate/polyethylene glycol (CA/PEG300) conjugated with silica nanoparticles (SNPs). Experimental data showed that the conjugation of SNPs changed the surface properties as dense and asymmetric composite structure. The results were explicitly determined by the permeability flux and salt rejection efficiency of the PM-SNPs membranes. The effect of SNPs conjugation on MgSO4 salt rejection was more significant in magnitude than on permeation flux i.e. 2.38 L/m(2)h. FTIR verified that SNPs were successfully conjugated on the surface of PM membrane. DSC of PM-SNPs shows an improved Tg from 76.2 to 101.8 °C for PM and PM-S4 respectively. Thermal stability of the PM-SNPs membranes was observed by TGA which was significantly enhanced with the conjugation of SNPs. The micrographs of SEM and AFM showed the morphological changes and increase in the valley and ridges on membrane surface. Experimental data showed that the PM-S4 (0.4 wt% SNPs) membrane has maximum salt rejection capacity and was selected as an optimal membrane.