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While dispersing graphene in water is a formidable challenge, π–π stacking between graphene oxide (GO) and graphene is known to enable the dispersion of graphene in water.

Superhydrophilic zwitterions on the membrane surface have been widely exploited to improve antifouling properties. However, the problematic formation of a <20 nm zwitterionic layer on the hydrophilic surface remains a challenge in wastewater treatment. In this work, we focused on the energy consumption and time control of polymerization and improved the strong hydrophilicity of the modified polyvinylidene difluoride (PVDF) membrane. The sulfobetaine methacrylate (SBMA) monomer was treated with UV-light through polymerization on the PVDF membrane at a variable time interval of 30 to 300 s to grow a poly-SBMA (PSBMA) chain and improve the membrane hydrophilicity. We examined the physiochemical properties of as-prepared PVDF and PVDF–PSBMAx using numeric analytical tools. Then, the zwitterionic polymer with controlled performance was grafted onto the SBMA through UV-light treatment to improve its antifouling properties. The PVDF–PSBMA120s modified membrane exhibited a greater flux rate and indicated bovine serum albumin (BSA) rejection performance. PVDF–PSBMA120s and unmodified PVDF membranes were examined for their antifouling performance using up to three cycles dynamic test using BSA as foulant. The PVDF-modified PSBMA polymer improved the antifouling properties in this experiment. Overall, the resulting membrane demonstrated an enhancement in the hydrophilicity and permeability of the membrane and simultaneously augmented its antifouling properties.

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Water and electricity shortages constitute a global energy crisis that cannot be ignored. The sun is an unlimited source of energy, and oceans provide abundant water and renewable energy resources. In this study, poly-(vinylidene fluoride) (PVDF)/graphene solar evaporator membranes are fabricated for simultaneous freshwater production and power generation. Graphene addition transformed the PVDF crystal from the α-phase to the piezoelectric self-assembly β-phase. The resulting membrane is used to convert the mechanical energy of waves to electrical energy. The membrane has an output voltage of 2.6 V (±1.3 V) and an energy density of 2.11 Wm −2 for 1 Hz simulated waves, which are higher than values reported in the literature. The stacked graphene and polymer formed a wood-lumens-like mesoporous structure with a photothermal effect. Under one sun illumination, the water production rate is 1.2 kg m −2 h −1 , and the solar-thermal energy conversion efficiency is 84%. Finally, a prototype is built to prove a single evaporator's feasibility that can simultaneously obtain freshwater and generate electricity. Thus, this membrane serves as an ocean wave power generation device that can provide all-weather energy generation, convert stored electrical energy into thermal energy at night and on cloudy days, and continuously provide safe drinking water.

Direct contact membrane distillation (DCMD) has been conducted to treat hydraulic fracturing-produced water using polyvinylidenedifluoride (PVDF) membranes. Tailoring the surface properties of the membrane is critical in order to reduce the rate of adsorption of dissolved organic species as well as mineral salts. The PVDF membranes have been modified by grafting zwitterion and polyionic liquid-based polymer chains. In addition, surface oxidation of the PVDF membrane has been conducted using KMnO4 and NaOH. Surface modification conditions were chosen in order to minimize the decrease in contact angle. Thus, the membranes remain hydrophobic, essential for suppression of wetting. DCMD was conducted using the base PVDF membrane as well as modified membranes. In addition, DCMD was conducted on the base membrane using produced water (PW) that was pretreated by electrocoagulation to remove dissolved organic compounds. After DCMD all membranes were analyzed by scanning electron microscopy imaging as well as Energy-Dispersive X-Ray spectroscopy. Surface modification led to a greater volume of PW being treated by the membrane prior to drastic flux decline. The results indicate that tailoring the surface properties of the membrane enhances fouling resistance and could reduce pretreatment requirements.

The development of science and technology is accompanied by a complex composition of multiple pollutants. Conventional passive separation processes are not sufficient for current industrial applications. The advent of active or responsive separation methods has become highly essential for future applications. In this work, we demonstrate the preparation of a smart electrically responsive membrane, a poly­(vinylidene difluoride) (PVDF)–graphene composite membrane. The high graphene content induces the self-assembly of PVDF with a high β-phase content, which displays a unique self-piezoelectric property. Additionally, the membrane exhibits excellent electrical conductivity and unique capacitive properties, and the resultant nanochannels in the membrane can be reversibly adjusted by external voltage applications, resulting in the tailored gas selectivity of a single membrane. After the application of voltage to the membrane, the permeability and selectivity toward carbon dioxide increase simultaneously. Moreover, atomic-level positron annihilation spectroscopic studies reveal the piezoelectric effect on the free volume of the membrane, which helps us to formulate a gas permeation mechanism for the electrically responsive membrane. Overall, the novel active membrane separation process proposed in this work opens new avenues for the development of a new generation of responsive membranes.