PVDF Research Articles

Fouling mitigation of microcrystalline cellulose-blended poly(vinylidene fluoride) membranes in protein separation

ABSTRACT Modifications of polymeric membranes are necessary to improve the membrane characteristics. The composite membrane of Poly(vinylidene fluoride)_Microcrystalline cellulose (PVDF_MCC) was prepared using dimethylacetamide/lithium chloride (DMAc/LiCl) as co-solvent to dissolve the MCC in the casting solution. The prepared membrane was characterized by using the FTIR, SEM, contact angle, and the water permeates flux. The improvement of hydrophilicity and pore structure with the incorporation of MCC was observed which led to the increment of the water and permeate flux. Indication from the rheological study suggested that the casting solutions with MCC presented the influence on the composite membrane’s pore structure as a significant viscosity increment was observed. This can be examined from the larger pore and elongated finger-like structure of the membrane morphology compared to the pristine membrane. The rejection rate of the protein increased from 85% to 97% after the incorporation of MCC in the PVDF membrane. The utilization of a low-cost and environmentally friendly additive that MCC has to offer helps to improve the antifouling properties of PVDF membranes for the efficient removal of BSA in water.

One-step fabrication of Polyvinylidene fluoride membranes enriched with electroactive β-Phase for secondary battery separators via simultaneous near infrared radiation and electrospinning

This study reports a one-step fabrication method to prepare polyvinylidene fluoride (PVDF) membranes enriched with electroactive β-Phase in application for secondary battery separator using near infrared radiation (NIR) heated electrospinning techniques. The electrospun PVDF fibrous membranes with NIR heating applied were investigated by various characterizations and measurements. The results present that NIR heating during electrospinning not only increased the β phase content and mechanical strength of the PVDF membranes but also improved the electrochemical performances, suggesting its potential suitability in the battery separator applications.

Preparation of Graphene Oxide (GO) incorporated-Polyvinylidene Fluoride (PVDF) Nanofiltration Membrane with Alkaline Post-Treatment for Textile Wastewater Treatment

The purpose of this research is to study the potential of polyvinylidene fluoride (PVDF) polymer incorporated with graphene oxide (GO), following with the alkaline etching post-treatment process for dye waste water treatment. Its anti-oxidation properties of PVDF, have led to its choice as a host polymer due to its high thermal stability, great organic selectivity, and excellent chemical and mechanical resistance. In addition, the post-treatment with a NaOH solutions of varied concentration ranging from 0 M to 0.2 M for 30 minutes was conducted in alter the morphology of the fabricated membrane with the aim to increase the perm-selectivity of the membranes. Besides, the fabricated membranes were further characterized in terms of the chemical and physical properties using Fourier-Transform Infrared Spectroscopy (FTIR), Contact Angle (CA), Ultraviolet Visible spectroscopy (UV-Vis), Atomic Microscopy (AFM) and Scanning Electron Microscopy (SEM). The experimental results showed that the post-treatment has decreased the membrane flux of dye wastewater. Based on the obtained result, as the concentration of NaOH solution increased, the permeability increased. While the overall dye rejection of the membrane remained of above 90 %.

Improving O₂ Absorption in PVDF Membrane with Cross-Linked Polymer Coatings

Surface modification of polyvinylidene fluoride (PVDF) membranes using various polymers, including chitosan, nylon, dopamine, and EDA, was examined through SEM and FTIR analyses. SEM imaging unveiled the preservation of membrane porosity post-modification, affirming successful polymer integration without pore obstruction. Nylon coatings induced alterations in surface morphology, with enlarged pore apertures and roughened surfaces attributed to formic acid exposure during dissolution. FTIR spectroscopy confirmed the presence of the respective polymers, exhibiting characteristic peaks for each. Notably, membranes coated with EDA exhibited enhanced CO2 absorption flux owing to their inherently hydrophilic nature and larger pore dimensions. Optimization of EDA coating parameters, including deposition time and concentration, revealed a direct correlation between increased EDA deposition and enhanced CO2 absorption flux, emphasizing the significant impact of these parameters on membrane performance in gas absorption. Consequently, tailored surface modifications offer a promising avenue for enhancing membrane functionality in gas separation applications

Enhancing Interfacial Lithiophilicity and Stability with PVDF/In(NO3)3 Composite Separators for Durable Lithium Metal Anodes

Separator modification is a promising method for advancing lithium metal anodes; however, achieving homogeneous lithium-ion flux and uniform plating/stripping processes remains challenging. In this work, we introduce a novel approach by developing a composite separator, termed PVDF-INO, which integrates In(NO3)3 (INO) into polyvinylidene fluoride (PVDF) to create a 12 μm thick layer. This addition significantly enhances the interaction between the separator and the electrolyte, creating a lithophilic matrix that ensures an even distribution of lithium ions. This uniform ion distribution promotes consistent lithium deposition and dissolution, resulting in a durable, dendrite-free lithium metal anode. Moreover, the PVDF-INO separator not only enhances the affinity with electrolytes but also maintains stable lithium-ion flux, which is essential for reliable and safe battery operation. Consequently, it sustains operation over 750 h in a Li||Li symmetric battery configuration, with a low overpotential of just 28 mV. Additionally, full cells equipped with LiFePO4 cathodes and the PVDF-INO separator exhibit superior cycling performance, maintaining a capacity retention of 92.9% after 800 cycles at 1 C. This work paves the way for significant advancements in the field of lithium metal batteries, offering a promising solution to longstanding energy storage challenges.

Instantaneous reduction of inkjet-printed graphene oxide on PVDF nanofibers for high-performance ultralight flexible supercapacitors

As the demand for innovative electronic devices continues to grow, flexible electronic products which offer a solution capable of adapting to various shapes and deformations, are increasingly gaining prominence. This study innovatively uses electrospun polyvinylidene fluoride (PVDF) nanofibers as substrates and employs reactive inkjet printing (RIP) technology to deposit and instantaneously reduce graphene oxide (GO), fabricating ultralight flexible all-solid-state supercapacitors. To verify that PVDF nanofibers as substrates can facilitate the uniform deposition of GO ink during inkjet printing and prevent the dispersion of GO into the internal structure, thereby achieving good capacitive performance with the fewest layers of printing, this study analyzes and compares the capacitive performance differences among 1rGO/PVDF, 3rGO/PVDF, and 5rGO/PVDF samples. The results have been confirmed that the GO ink was effectively instantaneously in-situ reduced by l-ascorbic acid (AA) to rGO by RIP system, and the specific capacitance of 1rGO/PVDF electrode was founded of 83.29 F/g at a current density of 2 A/g from the GCD analysis with a corresponding energy density of 7.5 Wh kg−1 and power density of 1.04 kW kg−1. The 1rGO/PVDF supercapacitor exhibits excellent electrochemical stability, maintaining 93 % efficiency after 4000 charge-discharge cycles at a current density of 2 A/g.

PVDF/Al2O3/Gd2O3 layers splitter with first-order suppression functionality

In the realm of optical component design, the proposed multilayer grating splitter represents a significant breakthrough. For the triple-layered grating in this paper, it combines the outstanding optical properties of polyvinylidene fluoride (PVDF), aluminum oxide (Al2O3), and gadolinium oxide (Gd2O3) to achieve high-efficiency outputs for both the 0th and −2nd orders under secondary Bragg angle incidence conditions. The diffraction efficiencies for both TE and TM polarizations exceed 97%, with energy uniformity surpassing 99%. These results highlight the potential of this design in precision beam control applications. The splitter's performance benefits from the intrinsic material properties and optimally designed structural dimensions, which enhance transparency and thermal stability under operational conditions. Through rigorous design and optimization, including modal methods and simulated annealing algorithms, the device achieves exceptional uniformity in diffraction efficiency, which is crucial for high-resolution spectroscopy and precision optical measurement applications.

Microwave-Assisted Oxidative Degradation of Poly(vinylidene fluoride-co-hexafluoropropylene) Copolymers: Preparation, Characterization, and Reaction Mechanism

Microwave-Assisted Oxidative Degradation of Poly(vinylidene fluoride-<i>co</i>-hexafluoropropylene) Copolymers: Preparation, Characterization, and Reaction Mechanism

Enhanced microwave absorption and mechanical performance of polyvinylidene fluoride thin films embedded with novel activated carbon and manganese ferrite

Enhanced microwave absorption and mechanical performance of polyvinylidene fluoride thin films embedded with novel activated carbon and manganese ferrite

Polyacrylonitrile Based Triblock Copolymer Binder Enabling Excellent Performance toward LiNi0.5Mn1.5O4 and Sulfur Based Batteries.

There is an urgent need for lithium-ion batteries with high energy density to meet the increasing demand for advanced devices and ecofriendly electric vehicles. Spinel LiNi0.5Mn1.5O4 (LNMO) is the most promising cathode material for achieving high energy density due to its high operating voltage (4.75 V vs Li/Li+) and impressive capacity of 147 mAh g-1. However, the binders conventionally used are prone to high potential and oxidation at the cathode side, resulting in a loss of the ability to bond active material and conductive agent integrity. This can lead to severe capacity fading and irreversible battery failure. This study demonstrates that incorporating acrylic anhydride and methyl methacrylate into conventional acrylonitrile through solution polymerization improves the binding energy and voltage resistance. The results indicate that the triblock poly(acrylonitrile-methyl methacrylate-acrylic anhydride) (PAMA) binder has a much higher peeling strength (0.506 N cm-1) compared to its polyvinylidene fluoride (PVDF) counterpart (0.3 N cm-1), making it a more feasible strategy. When assembled with LiNi0.5Mn1.5O4, the PAMA based electrode maintains a capacity retention of 70.7% after 800 cycles at 0.1 C, which is significantly higher than the 33.9% retention of the PVDFbased electrode. This is due to the large number of polar groups, including ─C≡N and ─C═O, on PAMA, which are conducive to adsorbing lithium polysulfide. The S@PAMA electrode is tested and maintained a capacity value of 628.7 mAh g-1 after long-term cycling, confirming its ability to effectively suppress the shuttle effect.

Development of conductive two-dimensional metal-organic frameworks self-cleaning membrane for enhanced antibiotics rejection and sustainable fouling mitigation

In this study, a novel electroactive NF membrane was constructed for ultrafast rejection of antibiotics with high selectivity and self-cleaning by incorporating a conductive two dimensional metal-organic frameworks (Cu-HHTP) into porous polyvinylidene fluoride (PVDF) matrix with facile and scalable non-solvent induced phase inversion strategy. Cu-HHTP membrane showed two orders of magnitude higher permeability (198.4 L m−2 h−1·bar−1) than the commercial and most reported NF membranes without sacrificing rejection toward negatively charged tetracycline (95.4 %), positively charged vancomycin (99.9 %) and neutrally charged valinomycin (99.9 %). Interestingly, loading Cu-HHTP with hydrophilic and porous nature can break the permeability-rejection trade-off effect and the mechanism was due to the improved water channel and pollutants sieving. Furthermore, it has stable antibiotics rejection and high flux recovery rate of 93.9 % for long-term filtration of wastewater over 264 h with low energy consumption of 0.1007 W h/L and without adding chemical cleaning agents, which demonstrated its excellent fouling control and stability. This study may guide the development of advanced self-cleaning NF membranes tailored for removal of small molecular emerging contaminants.

Boosting piezoelectric properties of PVDF nanofibers via embedded graphene oxide nanosheets

Tremendous research efforts have been directed toward developing polymer-based piezoelectric nanogenerators (PENG) in a promising step to investigate self-charging powered systems (SCPSs) and consequently, support the need for flexible, intelligent, and ultra-compact wearable electronic devices. In our work, electrospun polyvinylidene fluoride (PVDF) nanofiber mats were investigated while graphene oxide (GO) was added with different concentrations (from 0 to 3 wt.%). Sonication treatment was introduced for 5 min to GO nanosheets before combined PVDF solution. A comprehensive study was conducted to examine the GO incremental effect. Microstructural and mechanical properties were examined using a scanning electron microscope (SEM) and a texture analyzer. Moreover, piezoelectric properties were assessed via various tests including impulse response, frequency effect, d33 coefficient, charging and discharging analysis, and sawyer tower circuit. Experimental results indicate that incorporation of GO nanosheets enhances piezoelectric properties for all concentrations, which was linked to the increase in β phase inside the nanofibers, which has a significant potential of enhancing nanogenerator performance. PVDF-GO 1.5 wt.% shows a notably higher enhancing effect where the electroactive β-phase and γ-phase are recorded to be boosted to ~ 68.13%, as well as piezoelectric coefficient (d33 ~ 55.57 pC/N). Furthermore, increasing impact force encouraged the output voltage. Also noted that the delivered open circuit voltage is ~ 3671 V/g and the power density is ~ 150 µw/cm2. It was observed that GO of concentration 1.5 wt.% recorded a conversion efficiency of ~ 74.73%. All results are in line, showing better performance for PVDF-GO 1.5 wt.% for almost all concentrations.

Prediction of a Novel Electromechanical Response in Polar Polymers with Rigid Backbones: Contrasting Furan-Derived Nanothreads to Poly(Vinylidene Fluoride).

Syn furan nanothreads have all oxygen atoms arranged on one side of the thread backbone; these polar threads present intriguing opportunities in electromechanical response owing to their rigid ladder-like backbone. We retrained a C/H/O reactive force field to simulate their response to external electric field for both end-anchored individual threads and bulk nanothread crystals, contrasting the results to those for poly(vinylidene fluoride) (PVDF) polymer. Whereas the field induces a length-independent torque in PVDF through backbone rotation about σ bonds, furan-derived nanothreads generate a length-dependent torque by progressively twisting their rigid backbone. This mode of response couples the rotational history of the electric field to axial tension in the anchored thread. In simulations of densely packed syn furan nanothread crystals without anchors, the crystals pole in a field (∼3 GV/m at 300 K) similar to that seen in simulations of PVDF, suggesting that crystals of polar nanothreads can be ferroelectric.

Ytterbium-doping effect on the electrochemical and piezoelectric properties of poly(vinylidene fluoride) films

Abstract The optimal molar ratio of poly(vinylidene fluoride) (PVDF): dimethyl sulfoxide (DMSO) was investigated that promoted the β-phase formation, used during the PVDF film synthesis. The solution cast method was used for doping the PVDF films with 1.5% w/v ytterbium (III) nitrate salt hexahydrate. In general, Yb-doping in PVDF films improves thermal resistance, promotes β-phase formation, modifies the monomer conformation, reduces reversibility to electrochemical processes, and increases the d33 coefficient of piezoelectricity. The β-phase formation caused by Yb-doping alters the internal structures of the trans-gauche-trans-gauche' (TGTG') and all-trans (TTTT) chains inside the polymeric network. The coexistence between the trans-gauche and all-trans structures provides in both films the α-phase and β-phase coexistence. The presence of self-polarized CH2-CF2 dipoles, where the concentration of fluorine remains the same and the CH2 drastically increases after Yb3+ incorporation. The quasi-reversible shape shown in both voltammetry cyclic curves is related to irreversible oxidation and reduction reactions. Yb-PVDF exhibits specific pseudocapacitance values that are 30% higher than those of the PVDF films. Finally, the piezoelectric properties were improved with ytterbium incorporation.

Effect of layered double hydroxide-graphene oxide modifier composition on characteristics of polyvinylidene fluoride based nanocomposite membranes in the separation of Cu2+

This research explored the modified polyvinylidene fluoride (PVDF) nanofiber membranes with a composite of layered double hydroxide (LDH) and graphene oxide (GO) to enhance biofouling resistance. The PVDF/LDH-GO nanocomposite membranes were synthesized via vacuum filtration. FTIR analysis confirmed nanocomposite formation with new peaks indicating the presence of GO and LDH. Variations in the LDH:GO ratio affected the physical, mechanical, and performance properties of the membranes. Based on SEM imaging, the 1:1 LDH: GO ratio exhibited the highest Young's modulus and smallest pore sizes. LDH-GO incorporation increased the mechanical strength, porosity, roughness, hydrophilicity, and pure water permeability of the PVDF membranes. The combination of these factors led to balanced permeability and selectivity values towards Cu2+ solution feeds. LDH-GO was proven effective in modifying the PVDF membrane surface for water treatment and inhibiting biofouling up to 64% against E. coli.

Influence of photothermal nanomaterials localization within the electrospun membrane structure on purification of saline oily wastewater based on photothermal vacuum membrane distillation

Today, synergistic combination of special nanomaterials (NMs) and electrospinning technique has emerged as a promising strategy to address both water scarcity and energy concerns through the development of photothermal membranes for wastewater purification and desalination. This work was organized to provide a new perspective on membrane design for photothermal vacuum membrane distillation (PVMD) through optimizing membrane performance by varying the localization of photothermal NMs. Poly(vinylidene fluoride) omniphobic photothermal membranes were prepared by localizing graphene oxide nanosheets (GO NSh) (1) on the surface (0.2 wt%), (2) within the nanofibers structure (10 wt%) or (3) in both positions. Considering the case 1, after 7 min exposure to the 1 sun intensity light, the highest temperature (∼93.5 °C) was recorded, which is assigned to the accessibility of GO NSh upon light exposure. The case 3 yielded to a small reduction in surface temperature (∼90.4 °C) compared to the case 1, indicating no need to localize NMs within the nanofibers structure when they are localized on the surface. The other extreme belonged to the case 2 with the lowest temperature of ∼71.3 °C, which is consistent with the less accessibility of GO NSh during irradiation. It was demonstrated that the accessibility of photothermal NMs plays more pronounced role in the membrane surface temperature compared to the light trapping. However, benefiting from higher surface temperature during PVMD due to enhanced accessibility of photothermal NMs is balanced out by decrease in the permeate flux (case 1: 1.51 kg/m2 h and case 2: 1.83 kg/m2 h) due to blocking some membrane surface pores by the binder. A trend similar to that for flux was also followed by the efficiency. Additionally, no change in rejection was observed for different GO NSh localizations.

Nano-silica modified with silane and fluorinated chemicals to prepare a superhydrophobic coating for enhancing self-cleaning performance

ABSTRACT Superhydrophobic coatings with excellent self-cleaning performance have attracted significant concerns from researchers. Although various superhydrophobic coatings with prominent superhydrophobic properties have been fabricated, most developed coatings are still inadequate in pipeline scale inhibition applications. In this work, nano-silica (nano-SiO2) was modified by silane coupling of vinyltriethoxysilane (VETS) and 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (PFTS) to prepare a superhydrophobic coating. Organosilicon of PFTS and VETS was grafted onto the surface of SiO2 for preparing the superhydrophobic coating with low surface energy, and the superhydrophobic coating was cured via poly(vinylidene fluoride) (PVDF). The results showed that the contact angle of the prepared silica-based superhydrophobic coating, denoted as VETS-PFTS@SiO2/PVDF, is 159.2°, exhibiting outstanding superhydrophobicity performance. Furthermore, the superhydrophobicity coating also showed satisfactory durability performance in 200 g load wear test after 50 cycles. Importantly, the superhydrophobic coating displayed promising mechanical durability, chemical stability performance, as well as maintained excellent superhydrophobic properties after being placed in water for 3 weeks, indicating the potential for long-term utilization. In the simulated scale inhibition test, it was found that the synthesized coating can also significantly decrease the deposition rate of CaCO3 and successfully enhance its scale inhibition performance.

Enhanced Removal of Cr (VI) by PEI/nFe3O4 Ultrafiltration Membranes Using Peristaltic Pump-Driven Dynamic Adsorption

In this study, Fe3O4 nanoparticles (nFe3O4) were loaded onto polyvinylidene fluoride ultrafiltration membranes and capped with polyethyleneimine in order to form PEI/nFe3O4 ultrafiltration membranes. We used a peristaltic pump as a driver for dynamic adsorption, and the PEI/nFe3O4 ultrafiltration membrane had a good ability to remove hexavalent chromium (Cr(VI)) from wastewater. The full permeate volume of the PEI/nFe3O4 ultrafiltration membrane was maximized at pH 3. Meanwhile, the removal of Cr(VI) from the wastewater reached 98% and reduced to trivalent chromium (Cr(III)). When the initial concentration of Cr(VI) increased, the active sites on the membrane would be filled and the removal efficiency of Cr(VI) would decrease. Meanwhile, the coexisting ions affect the removal efficiency of Cr(VI), and PO43- has a strong negative effect on the removal efficiency. PEI/nFe3O4 ultrafiltration membrane is an effective combination of multifunctional nanomagnetic materials and membrane materials, which can effectively remove hexavalent chromium from wastewater. The study provides a basis for future applications in the environmental remediation of low-concentration chromium-containing wastewater.

Influence of boron incorporated biphasic calcium phosphate on mechanical, thermal, and biological properties of poly(vinylidene fluoride) membrane scaffold

AbstractIn this paper, boron (B)‐doped biphasic calcium phosphate (BCP)/poly(vinylidene fluoride) (PVDF) membrane scaffolds were developed by the combination of non‐solvent induced phase separation and lyophilization processes. In addition, the effects of the synthesized B‐incorporated BCP powders on the properties of the fabricated scaffolds were investigated. The physicochemical and morphological properties of the scaffolds were characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy. The physical properties were evaluated by surface wettability and swelling measurements, whereas the mechanical properties were investigated by tensile strength measurements. The thermal behavior was determined by differential scanning calorimetry, the β‐crystallization ratio was calculated by FTIR, and the β‐phase structure was characterized by X‐ray diffraction. The bioactivity was evaluated in the simulated body fluid, and the cytotoxicity of the scaffolds was also investigated by performing in vitro cell culture experiments. The results showed that the incorporation of B into the PVDF matrix improved the hydrophilicity while reducing the degree of swelling of the scaffolds. Tensile strength was slightly reduced by the powder content, but yet the strength of all scaffolds was mechanically compatible with native bone. Increasing the B content up to 0.5 and 1 wt.% was improved the thermal properties, the β‐crystalline phase fraction, and thus the piezoelectricity. Furthermore, B‐doped BCP/PVDF‐based scaffolds significantly promoted bioactivity, cell viability, and proliferation without cytotoxicity, compared to the PVDF scaffold, depending on the B content. In conclusion, our results indicate that the PVDF‐based composites in the form of membrane scaffolds that support bone growth have the potential to be highly sought‐after candidates in the field of biomedical applications.

Fabrication of Flexible Double‐Gate Organic Thin Film Transistor For Tactile Applications

AbstractIn this work, the development of a flexible Double‐Gate (DG) organic thin film transistor (DG‐OTFT), and its employment is reported for the realization of multimodal tactile sensors. Due to the self‐encapsulation of the stacked DG architecture, highly stable organic transistors are obtained that show almost negligible degradation after 6 months. Moreover, such configuration is also very useful for the development of sensing devices. In the case, one of the two gates is used to bias and set the working point of the devices, whereas the second one is connected to a polyvinylidene fluoride(PVDF)‐capacitor, a pyro/piezoelectric material. It is demonstrated that the charge displacement induced by the PVDF capacitor due to an applied external pressure or due to a temperature variation led to a reproducible variation of the device's output current. Using this approach high‐performing multimodal tactile sensors are obtained with sensitivity to up to 241 nA N−1 and 442 nA °C−1 respectively.