Dynamic Water Contact Angle Research Articles

Achieving Antibiofouling on Microporous Membranes Prepared with a Green Solvent via Spraying an Aqueous Antifouling Copolymer Solution

This study highlights a comprehensive investigation into the fabrication and characterization of sustainable membranes for antifouling applications. It utilizes γ-valerolactone as a green solvent to obtain microfiltration PVDF membranes, and leverages spray-coating technique to modify these membranes. This research aims to enhance the surface and bulk properties of PVDF membranes while promoting sustainable practices. Chemical analyses of the membranes reveal that the surface and bulk of the membranes were successfully modified. Dynamic water contact angle measurements indicated that a 10 mg/mL coating solution (PVDF_10) resulted in the highest hydrophilicity. Different biofouling tests were conducted using proteins and bacteria. In adhesion tests with BSA, and E. coli, the PVDF_10 membrane demonstrated the highest resistance, reducing adhesion by approximately 83% and 94%, respectively. Additionally, cyclical water/bacterial filtration tests demonstrated that PVDF_10 membrane achieved a higher flux recovery ratio compared to commercial hydrophilic PVDF membranes. The modifications remained stable even after 6 weeks of immersion in water. This study highlights the potential of γ-GVL and the spray-coating technique as environmentally friendly solvents and modification techniques for producing green antifouling PVDF membranes, aligning with sustainable practices and significantly enhancing membrane performance.

Facile and controlled dual-step modification with enhanced anti-fouling performance in polyvinylidene fluoride membranes

Water scarcity and pollution pose significant challenges, necessitating advancements in water treatment technologies. Among various solutions, ultrafiltration membranes, especially those crafted from polyvinylidene fluoride (PVDF), are favored for their mechanical robustness and chemical stability. However, their practical application is often limited by severe membrane fouling due to the inherent hydrophobicity of PVDF. This project introduces a straightforward, controlled method to enhance the anti-fouling properties of PVDF membranes, utilizing a blend of cellulose acetate (CA). The process involves a two-step modification of hydrolysis followed by quaternization, effectively increasing hydroxyl group presence and facilitating subsequent chemical reactions. The optimized membranes achieve a dynamic water contact angle of 0° within 30 s and maintain an electroneutral surface at pH 7.1. With a mean pore size reduction from 28.6 nm to 23.9 nm and an impressive drop in the irreversible fouling ratio from 36.9 % to 0.3 %, these modifications markedly improve the anti-fouling performance. This research demonstrates significant potential for enhancing the functionality of PVDF ultrafiltration membranes through post-fabrication modifications, offering significant benefits for water treatment applications.

A green zwitterionic bi-continuous membranes prepared by dual-bath procedure for mitigating biofouling during bacterial removal from water

This work explores the possibility of forming green microfiltration antifouling membranes based on polyvinylidene fluoride (PVDF) and a zwitterionic copolymer derivative of sulfobetaine methacrylate (SBMA), utilizing gamma-valerolactone (GVL) as the solvent and a mixture of ethanol and water as non-solvents. Efforts were initially focused on adjusting the immersion time of the matrix polymer in alcohol alone to obtain a porous structure, and 15 s were sufficient to achieve a symmetric, open porous morphology. Next, the polymer/copolymer/solvent blend was characterized. While it did not show the characteristics of a fully miscible system, DLS and visual observations revealed the obtaining of a homogeneous (relatively narrow particle size) and transparent to translucent system. Thus, membranes could be cast, and were shown to be stable. The addition of the copolymer maintained the physical characteristics of microfiltration membranes, but an FT-IR analysis revealed its effect on the dominant crystalline polymorph (switching from β to α). The membrane wettability was enhanced in an important extent with a dynamic water contact angle (WCA) gradually falling to < 40° (while the virgin membrane's WCA remained about 138° all test long), and a hydration capacity reaching about 530 mg/cm3 against <10 mg/cm3 for the virgin membrane. It reflected on the antifouling abilities of the membranes as tested using bovine serum albumin, fibrinogen, Escherichia coli, and Stenotrophomonas maltophilia, with relative decreases in adsorption during static tests measured to be 95 %, 70 %, 91 % and 98 %, respectively. Finally, compared to the virgin membrane, the modified membrane featured improved flux recovery (32 % vs. 11 %), significantly higher rejection (98.9 % vs. 89.1 %) and lower irreversible fouling tendency (68 % vs. 89 %) during cyclic water/bacterial solution filtration in dead-end mode, making it potentially suitable for addressing bacterial pollution in wastewater.

Synthesis of liquid EPDM having ultra-low-viscosity for curing at room temperature

A serial of liquid ethylene–propylene–diene rubber (EPDM) with 5-ethylidene-2-norbornene (ENB) contents of 2.0–6.5 mol% were synthesized by using VOCl3 based catalysts. The obtained polymers have much low molecular weight with Mn = 4530–10180 g/mol (PDI = 3.5–7.1), consequently, these EPDMs without solvent have excellent flowability with the viscosity of 2198∼7460 mPa s at 25 °C. And the glass transition temperature as low as −85.9 °C was achieved. Impressively, these liquid EPDMs can be cured at 25 °C after 5 days. NMR analysis suggested that ethyl trichloroacetate acted as activator to chlorinate V(II) species to V(III), but also acted as polymer modifier to provide a chlorinated EPDM, which appeared to be essential for liquid EPDMs curing at low temperature. The dynamic water contact angle results demonstrated that the EPDMs had excellent wettability properties and surface properties. Thus, this work provided a facile way for one-pot synthesis of liquid EPDM containing functional group for curing at room temperature.

Temperature Dependence of the Dynamic Contact Angles of Water on a Smooth Stainless-Steel Surface under Elevated Pressures.

The temperature dependence of the dynamic contact angles (DCAs) of water on a metallic surface remains unclear, especially under elevated pressures. Here in this work, the advancing and receding contact angles (RCAs), as well as the contact angle hysteresis (CAH), of water on stainless-steel 316 (SS316) surfaces were studied using the dynamic sessile drop method for temperatures up to 300 °C and pressures up to 10 MPa. It was found that the temperature dependence of the DCAs exhibits a different pattern as compared to the piecewise linear decline of static contact angles. The advancing contact angle (ACA) remains nearly constant and does not decrease until the temperature becomes close to the saturated temperature. The decrease in ACA is attributed to evaporation, which reduces the advancement of energy barrier. The RCA linearly declines below 120 °C and remains stable above 120 °C. The increasing temperature enhances the pinning effect and changes the droplet receding mode. Under all pressures tested, the CAH demonstrates a "increase-constant-decrease" trilinear relationship with temperature. Furthermore, the mean solid surface entropy and solid-gas interfacial tension of SS316 were estimated to be 0.1152 mJ/(m2·°C) and 61.49 mJ/m2, respectively.

Bioinspired Superhydrophobic Nanocoating Based on Polydopamine and Nanodiamonds to Mitigate Bacterial Attachment to Polyvinyl Chloride Surfaces in Food Industry Environments.

Polyvinyl chloride (PVC) is commonly utilized as a food-contact surface by the food industry for processing and storage purposes due to its durability, ease of fabrication, and cost-effectiveness. Herein, we report a composite coating for the superhydrophobization of PVC without the use of polyfluoroalkyl chemistry. This coating rendered the PVC superhydrophobic, exhibiting a static water contact angle of 151.9 ± 0.7° and a contact angle hysteresis of only 3.1 ± 1.0°. The structure of this composite coating, consisting of polydopamine, nanodiamonds, and an alkyl silane, was investigated by utilizing both scanning electron microscopy and atomic force microscopy. Surface chemistry was probed using attenuated total reflectance-Fourier transform infrared, and the surface wetting behavior was thoroughly characterized using both static and dynamic water contact angle measurements. It was demonstrated that the superhydrophobic PVC was cleanable using a food-grade surfactant, becoming wet in contact with high concentration surfactant solutions, but regaining its nonwetting property upon rinsing with water. It was demonstrated that the coating produced a 2.1 ± 0.1 log10 reduction (99.2%) in the number of Escherichia coli O157:H7 cells and a 2.2 ± 0.1 log10 reduction (99.3%) in the number of Salmonella enterica Typhimurium cells that were able to adsorb onto PVC surfaces over a 24 h period. The use of this fluorine-free superhydrophobic coating on PVC equipment, such as conveyor belts within food production facilities, may help to mitigate bacterial cross-contamination and curb the spread of foodborne illnesses.

Understanding the Intrinsic Water Wettability of Hexagonal Boron Nitride.

The water wettability of hexagonal boron nitride (hBN) has attracted a lot of research interest in the past 15 years. Experimentally, the static water contact angle (WCA) has been widely utilized to characterize the intrinsic water wettability of hBN. In the current study, we have investigated the effect of airborne hydrocarbons and defects on both static and dynamic WCAs of hBN. Our results showed that the static WCA is impacted by defects, which suggests that previously reported static WCAs do not characterize the intrinsic water wettability of hBN since the state-of-the-art hBN samples always have relatively high defect density. Instead, we found that the advancing WCA of freshly exfoliated hBN is not affected by the defects and airborne hydrocarbons. As a result, the advancing WCA on freshly exfoliated hBN, determined to be 79 ± 3°, best represents the intrinsic water wettability of hBN. A qualitative model has been proposed to describe the effect of airborne hydrocarbons and defects on the static and dynamic WCA of hBN, which is well supported by the experimental results. The finding here has important implications for the water wettability of 2D materials.

Synthesis and Characterization of Hydrophobic and Low Surface Tension Polyurethane

Polyurethane is a common polymeric coating, providing abrasion resistance, chemical durability, and flexibility to surfaces in the biomedical, marine, and food processing industries with great promise for future materials due to its tunable chemistry. There exists a large body of research focused on modifying polyurethane with additional functionalities, such as antimicrobial, non-fouling, anticorrosive action, or high heat resistance. However, there remains a need for the characterization and surface analysis of fluoro-modified polyurethanes synthesized with commercially available fluorinated polyol. In this work, we have synthesized traditional solvent-borne polyurethane, conventionally found in food processing facilities, boat hulls, and floor coatings, with polyurethane containing 1%, 2%, and 3% perfluoropolyether (PFPE). Polyurethane formation was confirmed by attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy, with the urethane band forming at 1730 cm−1 and the absence of free isocyanate stretching from 2275–2250 cm−1. X-ray photoelectron spectroscopy (XPS) was used to confirm perfluoropolyether polymerization with an increase in the atomic percentage of fluorine. Wettability and hydrophobicity were determined using a dynamic water contact angle with significant differences in advancing the water contact angle with the inclusion of perfluoropolyether blocks (PU–co–1PFPE 131.5° ± 8.0, PU–co–2PFPE 130.9° ± 5.8, and PU–co–3PFPE 128.8° ± 5.2) compared to the control polyurethane (93.6° ± 3.6). The surface orientation of fluorine supported the reduced critical surface tensions of polyurethane modified with PFPE (12.54 mN m−1 for PU–co–3PFPE compared to 17.19 mN m−1 for unmodified polyurethane). This work has demonstrated the tunable chemical qualities of polyurethane by presenting its ability to incorporate fluoropolymer surface characteristics, including low critical surface tension and high hydrophobicity.

Cellulose nanocrystals-microfibrils biocomposite with improved membrane performance

This study investigates eco-friendly membrane biocomposites derived from biomass, utilizing cellulose microfibrils (CMF) as the main membrane material. Cellulose nanocrystals (CNC), isolated from rice husk, were added as reinforcing fillers in CMF flat sheet membranes. CNC with concentrations of 0%, 10%, 20%, and 30% were employed. Scanning electron microscopy images revealed that CNC influenced the surface profile and the pore structure of the membranes, reducing the porosity by 23%. The empty areas formed by CMF interaction were effectively filled by CNC. This modified membrane resulted in an increase in NaCl rejection of up to 16%. Dynamic water contact angle demonstrated the role of CNC in enhancing permeability, with a shorter spreading time of 13 min. It was also confirmed by the highest flux of 351 L/m− 2h−1 under pure water flux conditions. Mechanical properties were significantly improved, with a 125% increase in tensile strength and a modulus of 329 MPa. The distribution of CNC within the membranes filled pores and enhanced CMF interaction, facilitated by abundant hydroxyl groups in CNC. Overall, this study highlights the potential of eco-friendly membrane biocomposites derived from biomass, offering valuable insights for the development of sustainable and efficient membrane materials.

Enhanced water permeability of hollow fiber composite reverse osmosis membrane using porous α-cellulose/polysulfone hollow fiber membrane as the substrate

The hollow fiber composite (HFC) reverse osmosis (RO) membrane with a special self-supporting structure has attracted a great deal of attention in the fields of separation and purification. However, low permeability is an urgent problem restricting its wide application. A porous polysulfone (PSF) hollow fiber support membrane was fabricated through the dry–wet spinning technique and hydrophilic α-cellulose © powder was incorporated in the PSF membrane matrix to improve the membrane’s water permeability. The HFC RO membrane was prepared via the interfacial polymerization process on the inner surface of the C/PSF support membrane. The membrane morphology and surface hydrophilicity were evaluated through scanning electron microscopy observation and dynamic water contact angle (WCA) measurement. The effects of α-cellulose incorporation on the separation performance of PSF hollow fiber membranes and HFC RO membranes were investigated. The results showed that the surface hydrophilicity and water permeability of the PSF membrane were significantly improved after the introduction of α-cellulose. The WCA of the modified PSF support membrane decreased from 84.6° for the neat PSF membrane to 70.25°, and the pure water flux can reach a maximum value of 102.1 L/(m2 · h) (0.1 Mpa), which was 1.3 times that of the pristine membrane. The HFC RO membrane using the hydrophilic modified PSF membrane as the substrate exhibited an enhanced water flux of 15.6 L/(m2 · h) and, meanwhile, the membrane salt rejection remained above 97.6% (1.0 wt% NaCl aqueous solution, 0.7 Mpa). The HFC RO membrane showed extremely high rejection rates (99%) for different dyes (congo red and methylene blue). No obvious performance deterioration was observed for the HFC RO membrane during continuous vacuum membrane distillation (VMD) experiments for 60 h.

Pectin-nanolignin composite films with water resistance, UV resistance, and antibacterial activity

In this work, pectin-lignin nanoparticle (LNP) composite films were prepared, the physical, antioxidant and antibacterial properties of the films systematically evaluated. The LNP were compatible with the pectin matrix, and the tensile strength (TS) and water contact angle (WCA) of the pectin-based films were enhanced by 164% and 56% at the optimum LNP loading of 3.0% (w/w). The results of dynamic WCA demonstrate the hydrophobic stability of pectin-LNP composite films. Even trace amounts of LNP (1.0%, w/w) were found to significantly improve the mechanical properties (TS improved 67.33%), hydrophobicity (WCA improved 48.83), and water barrier properties (the water vapor permeability decreased by 25.30%) of the pectin-based films. The tight entanglement and strong positive interaction between pectin and LNP promote the formation of dense structures, which is beneficial to the film properties. In addition, all pectin-LNP composite films almost completely shield the UVB (320-275 nm) and UVC (275-200 nm) spectrum, along with most of the UVA (400–320 nm) spectrum, which demonstrates their strong anti-ultraviolet performance. In terms of bioactivity, the addition of LNP significantly enhanced the DPPH radical scavenging ability (maximum boost is 6.33 times) and antibacterial ability (maximum inhibition rate was 78.79 for S.aureus and 47.80% for E.coli) of the pectin film. These results suggest that the pectin-LNP composite film are promising active packaging materials for food preservation/packaging applications.

Dynamic Wetting of Ionic Liquid Drops on Hydrophobic Microstructures.

Ionic liquids (ILs)─salts in a liquid state─play a crucial role in various applications, such as green solvents for chemical synthesis and catalysis, lubricants, especially for micro- and nanoelectromechanical systems, and electrolytes in solar cells. These applications critically rely on unique or tunable bulk properties of ionic liquids, such as viscosity, density, and surface tension. Furthermore, their interactions with different solid surfaces of various roughness and structures may uphold other promising applications, such as combustion, cooling, and coating. However, only a few systematic studies of IL wetting and interactions with solid surfaces exist. Here, we experimentally and theoretically investigate the dynamic wetting and contact angles (CA) of water and three kinds of ionic liquid droplets on hydrophobic microstructures of surface roughness (r = 2.61) and packing fraction (ϕ = 0.47) formed by micropillars arranged in a periodic pattern. The results show that, except for water, higher-viscosity ionic liquids have greater advancing and receding contact angles with increasing contact line velocity. Water drops initially form a gas-trapping, CB wetting state, whereas all three ionic liquid drops are in a Wenzel wetting state, where liquids penetrate and completely wet the microstructures. We find that an existing model comparing the global surface energies between a CB and a Wenzel state agrees well with the observed wetting states. In addition, a molecular dynamic model well predicts the experimental data and is used to explain the observed dynamic wetting for the ILs and superhydrophobic substrate. Our results further show that energy dissipation occurs more significantly in the three-phase contact line region than in the liquid bulk.

Organosilicon-Based Plasma Nanocoating on Crust Leather for Water-Repellent Footwear.

In this study, functional nanocoatings for water-repellent footwear leather materials were investigated by chemical plasma polymerisation by implanting and depositing the organosilicon compound hexamethyldisiloxane (HMDSO) using a low-pressure plasma system. To this end, the effect of monomers on leather plasma deposition time was evaluated and both the resulting plasma polymers and the deposited leather samples were characterised using different experimental techniques, such as: Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). In addition, leather samples were tested by standard tests for color change, water resistance, surface wetting resistance and dynamic water contact angle (DWCA). The resulting polysiloxane polymers exhibited hydrophobic properties on leather. Furthermore, these chemical surface modifications created on the substrate can produce water repellent effects without altering the visual leather appearance and physical properties. Both plasma coating treatments and nanocoatings with developed water-repellency properties can be considered as a more sustainable, automated and less polluting alternative to chemical conventional processing that can be introduced into product-finishing processes in the footwear industry.

Robust superhydrophobic and icephobic surface based on Teflon AF coated multiscale hierarchical ZnO/Cu2O nanostructures

We demonstrate hetero-nanostructured rough surface with solution based hydrophobic coating for robust superhydrophobic (SH) properties. The copper foil was anodically etched to generate Cu2O micro-needles and then ZnO nanorods were grown on Cu2O to create ZnO/Cu2O micro-nano hierarchical rough surface. A thin layer of Teflon AF was applied as a low surface energy coating on the top of the hierarchical surface. These surfaces were characterized for their structural phases using the X-ray diffraction technique and multiscale hierarchical surface morphology was confirmed using FESEM and AFM techniques. Wetting properties like static and dynamic water contact angle (CA) were analyzed using the advancing receding contact angle (ARCA) technique. This surface shows superhydrophobic properties with static CA of 157° and a roll-off angle of 3°. The durability of the SH surfaces was examined by water droplet impact for a range of velocities. The droplet rebounding is consistently seen up to Weber number, We ∼ 220. When the SH surface was cooled to −10 °C, dropwise condensation takes place. In this case, self-propelled jumping of droplets via multiple coalescences of microdroplets was observed. In the freezing rain condition, this surface exhibits poor adhesion to ice formation demonstrating an icephobic property. The surface retains SH properties even to the UVC exposure of about 12 J/cm2. The fabrication of the SH surface involves solution-based processes which are scalable to mass production for applications ranging from enhanced heat conduction to water-repellent coatings.

Water flux enhancement of PVDF membrane by a facile coating method for vacuum membrane distillation

Vacuum membrane distillation (VMD) has received considerable attention from both academia and industry. During VMD, the liquid-vapor interface is supported by a porous hydrophobic membrane to prevent wetting of the membrane pores and allow only vapor to pass through. Therefore, it is advantageous for the production of high-purity water by desalination, and improving the membrane performance has attracted significant attention. In this work, we present a facile method of modifying polyvinylidene difluoride (PVDF) membranes with a fluorine-containing ionic liquid (BPPF6) to improve the membrane hydrophobicity and antiwetting and antifouling properties. The dynamic water contact angle of the membrane increased from 124.5 ± 0.3° to 136.7 ± 0.1°, and the VMD water flux increased by 14.2% for treating 3.5 wt% NaCl aqueous solution at 45 °C.

Impact of an engineered micro-patterned interface on chitosan/glycerol membranes for wound healing

Biomimetic materials are of great significance in wide applications. As a bioactive polysaccharide, chitosan (CS) has attracted much attention in multiple fields. Inspired by the natural shark skin interface, herein, we proposed a methodology to obtain serial biomimetic CS/glycerol membranes via a facile mold casting and solvent evaporation process under mild aqueous conditions. The surface morphology, chemical structures, and physical characteristics of the developed membranes were determined by scanning electron microscopy, Fourier transformed infrared spectroscopy, tensile measurement, water vapor transmission rate, liquid uptake behavior, solubility, and dynamic water contact angle tests. Furthermore, in vitro and in vivo biological assays were performed, including antibacterial ability, hemostatic performance, hemolytic reaction, cytotoxicity evaluation, and contaminated wound healing assessment. Compared with the flat membranes, the micro-patterned CS/glycerol membranes show the higher water-absorbing ability (up to ca. 26-fold@30 min), moderate tensile strength (8.5–14.7 MPa), superior bacteriostasis (84.9% to 98.6% against S. aureus, 84.3% to 99.6% against E. coli), decent hemostat efficacy (within 75.7 s), low hemolysis rates (less than 0.5%), and benign cytotoxicity (84.2% to 98.4% of viability), which favor promoting contaminated wound healing. Thus, the biomimetic micro-patterned membranes improve bioactive performance and show the merits of simple operation, low cost, and easy scale-up. All these properties indicate that the hybrid micro-patterned membrane could be used as a suitable candidate for dermal wound dressings and open up the insights for developing other bionic interfaces in future potential applications.

Silicon carbide microfiltration membranes for oil-water separation: Pore structure-dependent wettability matters

Both the pore size and surface properties of silicon carbide (SiC) membranes are demonstrated to significantly affect their separation efficiency when used for oily water treatment. However, the potential influences of open porosity together with the pore size of SiC membranes on their surface properties and oil-water separation performance have rarely been investigated. In this work, porous SiC ceramic membranes with tunable open porosity and pore size were purposely prepared and selected to systematically study the effect of pore structure-dependent wettability on the oil-water separation performance. The measured pure water flux of selected membranes as a function of open porosity (34–48%) and pore size (0.43–0.67 μm) was well-fitted by using a modified H-P equation. Interestingly, the hydrophilicity of SiC membranes was improved with the increase in open porosity and pore size, as evidenced by the gradually decreased dynamic water contact angle and underwater adhesion of oil droplets. Further, the open porosity of SiC membranes was found to contribute more to the improved surface wettability. As a result, the stable flux of SiC membranes in oil-in-water (O/W) emulsions was increased by 24% with the increased open porosity while the oil rejection rate remained above 90%. This work quantitatively reveals the contributions of the pore structure to the surface wettability of ceramic membranes, and thus provides an effective pathway to improve their performance in oil-water separation.

Starch-Based Composite Films with Enhanced Hydrophobicity, Thermal Stability, and UV-Shielding Efficacy Induced by Lignin Nanoparticles.

Thehighly efficient utilization of lignin is of great importance for the development of the biorefinery industry. Herein, a novel "core-shell" lignin nanoparticle (LNP) with a diameter of around 135 nm was prepared, after the lignin was isolated from the effluent of formic acid fractionation via dialysis. In an attempt to endow composite materials with vital functionalities, the LNP was added to the starch film and the starch/polyvinyl alcohol (PVA) or starch/polyethylene oxide (PEO) composite film. The results showed that the hydrophobicity performance of the synthesized films was enhanced significantly. Specifically, the dynamic water contact angle value of the starch/PVA composite film with 1% (wt) addition of LNPs could be maintained as high as 122° for 180 s; the starch/PEO composite film also achieved an excellent water contact angle above 120°. The addition of LNPs promoted the formation of some rough structures on the film surface, as shown by the scanning electron microscopy images, which could repel the water molecules efficiently and are closely related to the enhanced hydrophobicity of the starch film. What is more, the as-prepared LNP conferred strengthened thermal stability and ultraviolet blocking properties on the starch composite film. The structural combination of the polymer film with LNPs holds the promise for providing advanced functionalities to the composite material with wide applications.

Construction of rough and porous surface of hydrophobic PTFE powder-embedded PVDF hollow fiber composite membrane for accelerated water mass transfer of membrane distillation

The construction of rough and porous hydrophobic membrane surface is expected to overcome the obstacles including low permeate water flux and membrane pore wetting which greatly restrict the development of membrane distillation (MD) technology. In this study, a rough and porous polytetrafluoroethylene (PTFE) powder-embedded polyvinylidene fluoride (PVDF) hydrophobic coating layer was compounded on the outer surface of PVDF hollow fiber support membrane by the dilute solution coating-phase inversion method. PVDF hollow fiber support membrane was fabricated by the dry-jet wet-spinning technique. PTFE powder was directly incorporated in PVDF dilute coating solution and embedded in the porous PVDF coating layer after the nonsolvent induced phase separation (NIPS). The variations of membrane morphology, surface chemical compositions, hydrophobicity and wetting resistance were investigated by scanning electron microscope (SEM), Attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), dynamic water contact angle (WCA) and liquid entry pressure (LEP) analysis. Membrane separation performance including desalination and ionic dyes removal properties was evaluated by VMD experiment. Compared with PVDF hollow fiber support membrane, both the surface hydrophobicity and the water permeability of the PTFE powder-embedded PVDF hollow fiber composite membrane (HFC) had obvious improvement. The surface WCA and permeate water flux increased from 92.6° and 11.3 kg/m2.h for PVDF support membrane to 133.6° and 26.8 kg/m2.h for the PTFE powder-embedded HFC membrane meanwhile NaCl rejection can be maintained above 99.9% (3.5 wt% NaCl aqueous solution at 50 °C and permeate pressure at 31.3 kPa). The separation performance of HFC membrane can remain stable without obvious pore wetting during the continuous MD operation for 36 h. Different from the desalination, porous hollow fiber membrane would adsorb two different charged dyes, Congo red (CR) and methylene blue (MB) to a certain extent, resulting in the decrease of membrane flux and the change of permeate water quality. Finally, the MD separation mechanism of inorganic salt, anionic dye and cationic dye by PTFE powder-embedded HFC membrane was proposed.

Superhydrophobic MS@CuO@SA sponge for oil/water separation with excellent durability and reusability

We present a superhydrophobic material based on commercially melamine sponge (MS) with great durability, recyclability, and excellent sorption performance. The fabrication process of this sponge is facile without using toxic reagents or sophisticated equipment and therefore it is simple to scale up. The CuO layer utilized to give a rough surface of the substrate (MS) was successfully prepared in a commercial microwave to seed copper nucleuses in an alkaline medium. Stearic acid (SA) plays a role as the self-assembled monolayer on the surface of the sponge skeletons. Throughout this study, the properties of the modified sponge were fully characterized, and the changes in wettability were carefully examined. Water contact angle (WCA) measurements revealed the excellent superhydrophobicity of the material with high static WCA of 165.1° and low dynamic WCA of 8°. Furthermore, the as-prepared sponge demonstrated high efficiency in separation (over 99.0%) of different oils from water. Notably, several unique properties of as-modified material were found, consisting of ultrafast sorption capacities of up to 32–52 times of its own weight by using 80 mL of each oil, outstanding reusability with good sorption capacity even after 40 cycles. Even under various harsh environments, the novel materials proved its outstanding durability and ultrafast sorption capacity of oils. The durability, recyclability, and superhydrophobic properties of the novel superhydrophobic sponge provide it a solid basis for oil-water separation applications through an ultrafast sorption capacity of oils as well as quick recovery of the oil by easy squeezing process.