Electrospun Differential Wetting Membranes for Efficient Oil–Water Separation

Separation of low viscous oil from water has attracted immense attention in recent times due to the ever‐increasing amount of oily industrial wastewater discharge and frequent oil spill accidents. Hence, there is a persistent demand for the fabrication of robust oil–water separation membranes. Herein, robust oil–water separation membranes are successfully fabricated by direct electrospinning of poly(vinylidene fluoride‐co‐hexafluoropropylene) and fluorinated polyhedral oligomeric silsesquioxane composite mixture. These hybrid membranes exhibit differential wetting (highly hydrophobic/superoleophilic) behavior for water and oil. The contact angle made by water and low viscous oil (hexane) with the membrane are measured to be 145 and 0° respectively. The nanofiber membranes efficiently separate low viscous oil from water in a single‐step with separation efficiency of nearly 100%. Furthermore, the results demonstrate that the membranes are robust and durable exhibiting differential wettability even after several oil–water separation cycles. The results reveal the potential of their use for real‐time industrial wastewater treatment applications.

     

Cellulose Sponge with Superhydrophilicity and High Oleophobicity Both in Air and under Water for Efficient Oil–Water Emulsion Separation

Oil–water emulsions stabilized by surfactants are fine dispersions of oil in water or of water in oil and difficult to separate which will lead to serious water pollution. A more recent development is the ability to fabricate oleophobic–hydrophilic surfaces in air, which are not easy to construct due to the difference surface tension between water and oil. Herein, a cellulose sponge with multipore structure is fabricated to increase the removal efficiency. Amphiphilic molecular brushes of polyethylene glycol with short perfluorinated end caps (F‐PEG) are grafted on cellulose sponges to solve the contradictory relation of hydrophilicity and oleophobicity and improve oil/water selective wettability and fouling resistance. Besides, stable superhydrophilicity and superoleophobicity under water, corrosive liquids, and high oleophobicity in air conditions are exhibited in the F‐PEG grafted porous cellulose sponges with textured surfaces (F‐g‐CS). And the separation efficiency and rate of F‐g‐CS with surface of nanopores are 99.92% and 180 L m⁻² h⁻¹, while that of micropores are 99.83% and 297 L m⁻² h⁻¹ only under gravity. It is demonstrated that the grafting F‐PEG molecules imparted F‐g‐CS of micropores surface with high flux and separation efficiency simultaneously. Furthermore, antifouling property and collection of water in oil–water mixture without fouling are possessed in F‐g‐CS.

     

Oil–Water Separation Using Superhydrophobic PET Membranes Fabricated Via Simple Dip‐Coating Of PDMS–SiO2 Nanoparticles

The surfaces of commercially available polyester (PET) and polypropylene (PP) are superhydrophobically modified via the deposition of polydimethylsiloxane (PDMS)‐coated SiO₂ nanoparticles (P‐SiO₂) and PDMS binder. The adhesion of P‐SiO₂ is stronger on PET than on PP due to a stronger chemical interaction between PET and PDMS, which is attributed to the higher surface energy of PET than PP. The waterproof ability and oil separation rate of the P‐SiO₂‐coated PET (dip‐PET) membranes are studied as a function of membrane thickness, and the influence of oil viscosity on the oil separation efficiency is investigated. Optimal membrane thickness should be selected in a given environment for the facile oil–water separation and the dip‐PET membrane is chemically stable and can be used repetitively for oil–water separation. Finally, an automated prototype instrument is introduced for the dip‐coating process. It is suggested that our dip‐PET is a promising solution for oil–water separation in real‐world oil‐spill applications.     

Preparation and characterization of nanofiltration membranes fabricated from poly(amidesulfonamide), and their application in water–oil separation

Nanofiltration membranes prepared from selected types of poly(amidesulfonamide) (PASA) targeted to retain either sucrose, raffinose, or β‐cyclodextrin were fabricated in conditions deduced from a chemometric method. Membrane performance was characterized by the permeation of solutions containing 1000 ppm carbohydrates and metal ions. To demonstrate the dependence of the membrane properties on the polymer structure, the separation characteristics of a series of four PASA homopolymers and four PASA copolymers were established. The results allowed us to screen out several promising PASA materials for the NF separation process. In addition, the superiority of the PASA materials, characterized by excellent retention and high flux rate, was evident from the results of a study comparing it with polysulfonamide, poly(ether amide), and commercially available regenerated cellulose. As a means of pollution control, the PASA NF membranes have been proven to be effective in removing oil from oily wastewater. Under an operating pressure of 2–3 psi, a constant flux of 5 L m^?2 h^?1 and 99.6% retention of a solution of 5000 ppm olive oil could be achieved with the PASA membranes over a period of 430 h. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1803–1810, 2003     

Synergetic Effects of Graphene Oxide and Clay on the Microstructure and Properties of HIPS/Graphene Oxide/Clay Nanocomposites

In this paper, double-network structure nanocomposite with improved mechanical and thermal properties were prepared using high-impact polystyrene as a matrix phase, clay and graphene oxide as effective reinforcing fillers through a facile solution intercalation method. The structure and morphology of nanocomposites were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction analysis, and the synergetic effects of clay and graphene oxide on the final properties were investigated using tensile, dynamic mechanical thermal analysis (DMTA) and thermogravimetric analysis (TGA) analysis. Mechanical analysis showed that the combination of graphene oxide and clay exerted a favorable synergistic effect on the tensile modulus and the yield strength of the ternary composite that are greatly improved as compared with neat high-impact polystyrene, high-impact polystyrene/graphene oxide, and high-impact polystyrene/clay binary composites due to the double-network structure formation between the nanofillers as confirmed by the direct morphological observations using transmission electron microscopy and scanning electron microscopy analysis. The viscoelastic behavior showed that storage modulus of ternary composite significantly improvement over than that of the pure matrix, high-impact polystyrene/graphene oxide and high-impact polystyrene/clay while network structure made. TGA and DMTA measurements also demonstrated that thermal stability of high-impact polystyrene matrix modified by graphene oxide and clay slightly enhanced during the creation of dual network structure of graphene oxide and clay. Our data suggest a potential application for the combination of graphene oxide and clay in graphene-based composite materials.     

One‐Pot Route for Fe@Poly(styrene‐co‐divinylbenzene) Foam with Robust Physical/Chemical Stability and Remote Magnetic Driven Capacity for Oil Removal

Magnetic and superhydrophobic materials with robust physical/chemical stability for controllable and remote magnetic driven capacity for oil removal under harsh environments are meaningful for oil–water separation but still a challenge. Herein, an alternative strategy to address this challenge is demonstrated by decorating poly(styrene‐co‐divinylbenzene) (PSDVB) on Fe foam via one‐pot solvothermal method. Different from previous magnetic and superhydrophobic materials, Fe foam is chosen to replace Fe₃O₄ nanomaterials. Thus, complicated preparation procedures and the high cost for Fe₃O₄ nanomaterials can be avoided. Additionally, PSDVB coating provides the whole foam with robust physical/chemical stabilities: i) the surface wettability can be maintained after 50 abrasion cycles or exposed in humid air (relative humidity: 90%) for 14 days, and ii) the surface wettability does not change under different pH solutions (3 < pH < 12) or highly salty solution (NaCl 10 wt%) for 6 h. Besides, outstanding separation efficiency (>99.9%), high durability (>70 times), and excellent oil flux (16 963–75 156 L m^?2 h^?1) can be realized under gravity. Most importantly, the foam continuously removes oil from confine place (on water surface or under water) under magnetic driven force.     

Investigation of the specific interfacial area of a palm oil–water system

Oil–water dispersions have many important applications in the chemical and oleochemical industries. A measure of the specific interfacial area of the dispersed phase provides a direct indication of the quality of the dispersion. In this study, the specific interfacial area for the palm oil–water system was determined using a microscopic technique. The effects of oil volume fraction, agitation speed and temperature on the specific interfacial area have been determined experimentally and an empirical correlation to predict the total specific interfacial area under different operating conditions is proposed. This correlation can be used in the design of reaction and non‐reaction systems using palm oil–water dispersions. Copyright © 2004 Society of Chemical Industry     

Gamma‐radiation initiated synthesis of Psyllium and acrylic acid‐based polymeric networks for selective absorption of water from different oil–water emulsions

Removal of water from the crude petroleum during its extraction and refining process is one of the major problems faced by petroleum industries, so in this study a superabsorbent has been synthesized from Psyllium and acrylic acid based polymers under the influence of gamma radiations using hexamine as a crosslinker. After optimizing various reaction parameters, the optimized superabsorbent has been tested for its selective water absorption capacity from different oil–water emulsions as a function of time, temperature, pH, and NaCl concentration. The synthesized superabsorbent has been found to be highly selective toward water absorption with maximum percent swelling of 8560% in petrol–water emulsion. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Chitosan–Graphene Oxide Composite Membranes for Solid-Phase Extraction of Pesticides

Solid-phase extraction (SPE) coupled to LC/MS/MS analysis is a valid approach for the determination of organic micropollutants (OMPs) in liquid samples. To remove the greatest number of OMPs from environmental matrices, the development of innovative sorbent materials is crucial. Recently, much attention has been paid to inorganic nanosystems such as graphite-derived materials. Graphene oxide has been employed in water-purification processes, including the removal of several micropollutants such as dyes, flame retardants, or pharmaceutical products. Polysaccharides have also been widely used as convenient media for the dispersion of sorbent materials, thanks to their unique properties such as biodegradability, biocompatibility, nontoxicity, and low cost. In this work, chitosan–graphene oxide (CS_GO) composite membranes containing different amounts of GO were prepared and used as sorbents for the SPE of pesticides. To improve their dimensional stability in aqueous medium, the CS_GO membranes were surface crosslinked with glutaraldehyde. The composite systems were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, swelling degree, contact angle, and mechanical measurements. As the GO content increased, a decrease in surface homogeneity, an improvement of mechanical properties, and a reduction of thermal stability of the CS-based membranes were observed. The increased dimensional stability in water, together with the presence of high GO amounts, made the prepared composite membranes more efficacious than the ones based just on CS in isolating and preconcentrating different hydrophilic/hydrophobic pollutants.     

Triple-Networked Hybrid Hydrogels Reinforced with Montmorillonite Clay and Graphene Nanoplatelets for Soft and Hard Tissue Regeneration

Hydrogel is a three-dimensional (3D) soft and highly hydrophilic, polymeric network that can swell in water and imbibe a high amount of water or biological fluids. Hydrogels have been used widely in various biomedical applications. Hydrogel may provide a fluidic tissue-like 3D microenvironment by maintaining the original network for tissue engineering. However, their low mechanical performances limit their broad applicability in various functional tissues. This property causes substantial challenges in designing and preparing strong hydrogel networks. Therefore, we report the triple-networked hybrid hydrogel network with enhanced mechanical properties by incorporating dual-crosslinking and nanofillers (e.g., montmorillonite (MMT), graphene nanoplatelets (GNPs)). In this study, we prepared hybrid hydrogels composed of polyacrylamide, poly (vinyl alcohol), sodium alginate, MMT, and MMT/GNPs through dynamic crosslinking. The freeze-dried hybrid hydrogels showed good 3D porous architecture. The results exhibited a magnificent porous structure, interconnected pore-network surface morphology, enhanced mechanical properties, and cellular activity of hybrid hydrogels.     

Separation of phenol–water mixture by membrane pervaporation using polyimide membranes

Separation of components of aqueous waste streams containing organic pollutants is not only industrially very important but also is a challenging process. In this study, separation of a phenol–water mixture was carried out by using a membrane pervaporation technique with indigenously developed polyimide membranes. The membranes were found to permeate water selectively. The total flux as well as that of the individual components were measured. The effect of lithium chloride modification of polyimide film on total flux was investigated. The total flux obtained with 2% lithium chloride modification was about 3.6 times higher than that obtained with virgin membrane. The effects of different parameters such as feed composition and temperature on flux, and separation factor were determined. With modified membrane, a separation factor as high as 18.0 was obtained for water at 27°C and with 8.0 wt % phenol solution. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 822–829, 2002     

Lipase immobilization on ionic liquid‐modified magnetic nanoparticles: Ionic liquids controlled esters hydrolysis at oil–water interface

Ester hydrolysis at oil–water interface by lipase covalently immobilized on ionic liquid‐modified magnetic nanoparticles was investigated. Magnetic supports with a diameter of 10–15 nm were synthesized by covalent binding of ionic liquids (chain length C₄ and C₈ and anions Cl^?, BF₄^?, and PF₆^?) on the surface of Fe₃O₄ nanoparticles. Lipase was covalently immobilized on Fe₃O₄ nanoparticles using ionic liquids as the coupling reagent. Ionic liquid‐modified magnetic nanoparticle‐grafted lipase preferentially located at the oil–water interface. It has higher catalytic activity than its native counterpart. A modified Michaelis–Menten model was used to elucidate the effect of stirring rate, aqueous–organic phase ratio, total amount of enzyme, and ester chain length. The influences of these conditions on esters hydrolysis at oil–water interface were consistent with the introduction of the ionic liquids interlayer. Ionic liquids could be used to control the oil–water interfacial characteristics during lipase catalyzed hydrolysis, and thus control the behavior of immobilized lipase. © 2011 American Institute of Chemical Engineers AIChE J, 2012     

Studying the Potential Application of Electrospun Polyethylene Terephthalate/Graphene Oxide Nanofibers as Electroconductive Cardiac Patch

Nowadays, engineering‐based cardiac patches aim to accelerate cardiac regeneration in myocardial infarcted tissues. Considering the fundamental role of cardiac electrophysiology in myocardial function, this study aims to investigate graphene oxide (GO) incorporation in the polyethylene terephthalate (PET) nanofibrous scaffold, as a conductive cardiac patch. The PET/GO nanocomposites are prepared using the uniaxial nozzle and coaxial nozzle electrospinning processes and comprehensively evaluated. The morphological observation indicates a uniform beaded free morphology with an average diameter of 147 ± 38 and 253 ± 67 nm for solid and core–shell nanocomposite fibers, respectively. Addition of GO to the PET nanofibers in a concentration of 0.05 wt% remarkably increases the Young modulus of mats from 30 ± 0.03 to 60 ± 0.02 and 69 ± 0.08 MPa for solid and core–shell nanofibers, respectively. Also, the electroconductivity is improved from 0.7 × 10^?6 to 1.175 × 10^?6 and 1.3 × 10^?6 S cm^?1 for solid and core–shell nanofibers, which are in the range of cardiac electroactivity values. PET/GO substrate interestingly supports human umbilical vein endothelial cells’ spreading morphology and cardiomyocyte elongated morphology, mainly where the GO nanosheets are distributed near the surface of nanofibers. In conclusion, the core–shell electrospun PET/GO nanocomposite fibers are suggested as a potential electroactive cardiac patch to improve cardiac cell attachment and proliferation.     

PCL–PEG–PCL triblock copolydiol-based waterborne polyurethane. I. Effects of the soft-segment composition on the structure and physical properties

This article examines the effects of the soft-segment composition on the structure and physical properties of waterborne polyurethane (WBPU) based on polycaprolactone–poly(ethylene glycol)–polycaprolactone (PCL–PEG–PCL) triblock copolydiol as the soft segment. The molecular weight of PEG in the soft-segment composition and soft-segment content (SSC) are varied in this study. The water-vapor permeability (WVP) for the WBPU-coated nylon fabric is also studied. The results showed that the glass transition temperatures (T_g's) of the soft segment decreased and its temperature range (ΔT_g's) narrowed with increase of SSC up to 63 wt % and decrease of the PEG molecular weight. The dynamic mechanical analysis results showed that the α-peak height of the soft segment increased with SSC when the SSC was less than 63 wt %. However, when SSC was more than 63 wt %, the α-peak height became smaller with increasing SSC due to the crystallization of the soft segment. At the same SSC, the number of spherulites was reduced and the spherulites become larger with decrease of the PEG molecular weight. As for the mechanical properties of the WBPU cast film, the breaking stress decreased and the breaking elongation increased with increasing SSC or decreasing PEG molecular weight. For the WBPU-coated nylon fabrics, either higher SSC or higher PEG molecular weight improves the WVP. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65:883–892, 1997     

Preparation of Carbonized Kapok Fiber/Reduced Graphene Oxide Aerogel for Oil-Water Separation

A carbonized composite aerogel was fabricated based on kapok fibers (KFs) and graphene oxide (GO) through hydrothermal and carbonizing reactions. The as-prepared carbonized kapok fiber/reduced graphene oxide (CKF/RGO) aerogel exhibited special features including light weight, fire resistance, stable structure, hydrophobicity, and oleophilicity. The wettability of the KF/GO aerogel was transformed to hydrophobicity after carbonization, which provided the CKF/RGO aerogel with a distinct ability for oil-water separation. The CKF/RGO aerogel was able to adsorb oil liquids up to 110 times of its own weight. The sorption capacity of the CKF/RGO aerogel was still higher than 90 % of the initial sorption capacity after eleven sorption-combustion cycles of n-hexane solvent.     

Synthesis and Bioactivity of Reduced Graphene Oxide/Alumina‐Noble Metal Nanocomposite Flakes

The aim of this study was to describe the modification of the bioactivity of Al₂O₃‐noble metal (Me = Ag, Au, or Pd) composite nanoparticles by the addition of graphene oxide and the formation of a RGO/Al₂O₃‐Me nanocomposite system. The nanocomposite flakes and Al₂O₃‐Me composite nanoparticles were widely characterized. The antibacterial effect was observed only for Al₂O₃‐Ag composite nanoparticles and RGO/Al₂O₃‐Ag nanocomposite flakes, while, in the case of RGO/Al₂O₃‐Ag, a more evident antibacterial effect against Staphylococcus aureus bacteria was observed compared with Al₂O₃‐Ag. In the case of other noble metals (Au, Pd), a slight growth‐stimulating effect was revealed for particular bacterial strains.     

Preparation and oil–water separation evaluations of polypropylene/low‐melt‐point polyester composites reinforced by thermal bonding and one‐step solution immersion

Nonwoven fabrics have been fabricated for oil–water separation, but simplifying the manufacturing processes is still a challenge. In this work, a facile and easily scaled up approach based on thermal bonding and one‐step solution immersion has been successfully developed to prepare nonwoven fabrics with high separation efficiency and flux of oil. Here, polypropylene (PP) and low‐melt‐point polyester (LPET) fibers with a unique sheath–core structure are employed to form PP/LPET nonwoven fabrics. Thermal bonding by hot press and hydrophobic treatment with 1H,1H,2H,2H‐perfluorodecyl‐1‐thiol (PFDT) are used to manufacture oil–water separation nonwoven fabrics. Effects of the ratio of LPET fibers and the concentration of PFDT are discussed in terms of mechanical properties, morphology, surface chemical composition, water contact angle and performance of oil–water separation and flux of the nonwoven fabrics. The results show that the strength of the nonwoven fabrics gradually increases with increasing ratio of LPET fibers. After immersion in PFDT, the nonwoven fabrics show high hydrophobicity with a water contact angle of 143°. They can be used to separate oil–water mixtures. The separation efficiency is 97–99% and the oil flux is 62 364.92 L m^?2 h^?1. This study provides a new prospect for simple introduction of a hydrophobic agent on a nonwoven fabric to achieve various functional oil–water separation materials. © 2020 Society of Chemical Industry