Fumed SiO2 nanoparticle reinforced biopolymer blend nanocomposites with high dielectric constant and low dielectric loss for flexible organic electronics

In the present study, fumed silica (SiO₂) nanoparticle reinforced poly(vinyl alcohol) (PVA) and poly(vinylpyrrolidone) (PVP) blend nanocomposite films were prepared via a simple solution‐blending technique. Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), X‐ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to elucidate the successful incorporation of SiO₂ nanoparticles in the PVA/PVP blend matrix. A thermogravimetric analyzer was used to evaluate the thermal stability of the nanocomposites. The dielectric properties such as dielectric constant (?) and dielectric loss (tan δ) of the PVA/PVP/SiO₂ nanocomposite films were evaluated in the broadband frequency range of 10^?2 Hz to 20 MHz and for temperatures in the range 40–150 °C. The FTIR and UV–vis spectroscopy results implied the presence of hydrogen bonding interaction between SiO₂ and the PVA/PVP blend matrix. The XRD and SEM results revealed that SiO₂ nanoparticles were uniformly dispersed in the PVA/PVP blend matrix. The dielectric property analysis revealed that the dielectric constant values of the nanocomposites are higher than those of PVA/PVP blends. The maximum dielectric constant and the dielectric loss were 125 (10^?2 Hz, 150 °C) and 1.1 (10^?2 Hz, 70 °C), respectively, for PVA/PVP/SiO₂ nanocomposites with 25 wt % SiO₂ content. These results enable the preparation of dielectric nanocomposites using a facile solution‐casting method that exhibit the desirable dielectric performance for flexible organic electronics. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44427.     

Electromagnetic interference shielding properties of graphene quantum-dots reinforced poly(vinyl alcohol)/polypyrrole blend nanocomposites

Graphene quantum dots (GQDs) reinforced poly(vinyl alcohol) (PVA)/polypyrrole (WPPy) nanocomposite films with various GQDs loadings were synthesized using the versatile solvent casting method. The structural and morphological properties of PVA/WPPy/GQDs nanocomposite films were investigated by employing Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. The thermogravimetric analysis revealed enhanced thermal stability of synthesized nanocomposites while enhanced dielectric properties were also observed. The maximum dielectric constant value for PVA/WPPy/GQDs nanocomposite films was observed to be ε = 6,311.85 (50 Hz, 150°C). The electromagnetic interference (EMI) shielding effectiveness (SE) of nanocomposite films was determined in the X-band (8–12 GHz) and Ku-band (12–18 GHz) frequency region. The EMI SE was found to be increased from 0.8 dB for the pure PVA film to 9.8 dB for the PVA/WPPy/GQDs nanocomposite film containing 10 wt% GQDs loading. The enhanced EMI shielding efficiency of nanocomposite films has resulted from the homogenous dispersion of GQDs in PVA/WPPy blend nanocomposites. Thus, the prepared nanocomposites are envisioned to utilize as a lightweight, flexible, and low-cost material for EMI shielding applications.     

Effects of Carbon Nanofiber on Dielectric Properties of PMN/CNFs/EP Composites

A kind of new composite material composed of piezoelectric ceramic lead magnesium niobate-lead zirconate-lead titanate (PMN)/carbon nanofibers (CNFs)/epoxy resin (EP) were prepared by a resin casting method. The effects of carbon nanofibers on dielectric properties of PMN/CNFs/EP composites were investigated in this paper. The concetration of CNFs had significant effects on dielectric constant, dielectric loss, dielectric frequency dependence and dielectric temperature dependence of PMN/CNFs/EP composites. When the content of CNFs increased from 0 to 0.8 wt% of the epoxy resin, the dielectric constant at 1 kHz increased sharply from 13.6 to 158, and the dielectric loss increased from 0.0524 to 2.59. In plots of the dielectric constant against frequency and dielectric loss against frequency, the dielectric constant and dielectric loss reduced dramatically at lower frequency ranging from zero to about 10⁵ Hz, then approach to be stable at frequency higher than 10⁵ Hz. Moreover, as to the effects of temperature on dielectric constant and dielectric loss of PMN/CNFs/EP composites, the dielectric constant of composite increased ranging from 25°C to 160°C, and the dielectric loss of composite also showed increase besides that with CNFs content 0.8 wt%.     

Hydrothermal Synthesis of Polyoxometalate Containing Cobalt Ion,and Its Polyurethane Composites for Dielectric Material Applications

ABSTRACT

Polyurethane (PU) composites were prepared with different diisocyanate and diol compounds by adding cobalt ion-based polyoxometalate (Co-POM) as reinforcement. For the determination of using potential in microelectronic applications, the dielectric behavior and dielectric constant of these PU composites were investigated and compared to pure polyurethane structures. For this aim, firstly, Co-POM with Keggin structure was obtained from ammonium heptamolybdate, 1,10-phenanthroline ligand and a cobalt (II) salt by hydrothermal synthesis technique. Then, polyurethane/Co-POM composites (PU/Co-POM) were prepared with ethylene glycol, nonaromatic diisocyanate and different amounts of Co-POM reinforcement (1%, 3%, 5% and 10%, w/w) by in situ polymerization and mix-blend technique. Obtained PU/Co-POM composites were characterized in detail by infrared spectroscopy, Elemental Mapping, Energy-dispersive X-ray spectroscopy (EDX) and X-ray powder diffraction (XRD) spectroscopy. The surface structure, morphology and roughness of PU/Co-POM composites were investigated by SEM and AFM analysis. The elemental maps of the PU/Co-POM surface were examined by EDX elemental mapping analysis methods. Thermal stability, Tg values and thermal decomposition temperatures of PU/Co-POM structures were determined by different thermal analysis techniques. Thermal analysis results showed that the PU/Co-POM composites are thermally stable up to approximately 200°C and Tg values of synthesized PU composites are seen between 54.72°C and 75.15°C. The dielectric properties and dielectric constants of the PU/Co-POM composites were determined in the frequency range 1 Hz to 1000 kHz at room temperature using impedance analyzer. Dielectric constants of these composites were ranged from 5.50 to 9.26 according to their polarizability and H-bonding ability of PU matrix structure. According to the dielectric measurements, the dielectric constants of the PU/Co-POM structures were significantly decreased compared to the pure PU structures.     

Effect of microstructure on the dielectric properties of poly(vinyl alcohol)–poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonate) composite films

Poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonate) (PEDOT–PSS) was blended with poly(vinyl alcohol) (PVA) to form 0, 10, 20, 30, 40, and 50 vol % PEDOT–PSS/PVA solutions, and their freestanding films were prepared with a simple and cost‐effective solution casting technique at 27 °C in the absence of additives. Field emission scanning electron microscopy images revealed changes in the cocontinuous network to a rodlike morphology in the composite films from 10 to 50 vol % PEDOT–PSS/PVA. The alternating‐current conductivity was found to obey Jonscher's power law. The obtained values of the dielectric constant at 27 °C were relatively high, and a maximum value of 6.7 × 10⁴ at 100 Hz for 40 vol % PEDOT–PSS'/PVA was observed. The dielectric loss attained a maximum value of about 10⁶ at 100 Hz for 40 vol % PEDOT–PSS/PVA. However, a decrease in the dielectric parameters was observed at 50 vol % PEDOT–PSS/PVA because of locally induced strain in the microstructure. The variations in polarization with respect to the applied electric field (P–E) were determined for 50, 100, and 500 Hz at 500 V for the freestanding composite films of lower concentrations up to 20 vol % PEDOT–PSS/PVA. In summary, the dielectric and P–E measurements confirmed that the electrical characteristics changed in accordance to the contribution from both resistive and capacitive sites in the PEDOT–PSS/PVA composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45079.     

Dielectric transition and ferroelectric properties of graphene oxide-barium titanate nanocomposites

Graphene oxide (GO)-barium titanate (BT) composite was prepared through sonication process at room temperature. The temperature dependent dielectric properties and transition of GO with different pellet thickness were studied. Electrical properties of GO-BT composites with different weight percentages of GO and BT (2:1, 1:1 and 1:2) from 30 to 200 °C were investigated. The dielectric constant was calculated as 3701 and 1296 for GO(2)-BT(1) and GO(1)-BT(1) composites respectively which are higher than that of BT at 1 kHz. The improvement of ε' is attributed to the formation of microcapacitors by GO sheets segregated by BT particles. Curie temperature of BT was suppressed in the composites and effect of GO on the dielectric properties of the composite is predominant. The dielectric peaks of GO at 50 and 170 °C were gradually shifted to high and low temperatures respectively with increasing BT content. Furthermore, polarization (P) vs electric field (E) was measured at room temperature specifying the decrease in ferroelectricity of composites from that of BT, indicating the highly conducting nature of these samples. The increasing content of GO in composite leads to decrease in remnant polarization because the introduction of GO would weaken the ferroelectricity of the composite. The present findings suggest that the new composite can be useful for fabrication of flexible electronic devices and high dielectric-based electronic and energy storage devices.     

Solution-processed white graphene-reinforced ferroelectric polymer nanocomposites with improved thermal conductivity and dielectric properties for electronic encapsulation

The recent surge in graphene research has stimulated interest in the investigation of various two-dimensional (2D) nanomaterials, including 2D boron nitride (BN) nanostructures. Among these, hexagonal boron nitride nanosheets (h-BNNs; also known as white graphene, as their structure is similar to that of graphene) have emerged as potential nanofillers for preparing thermally conductive composites. In this work, hexagonal boron nitride nanoparticles (h-BNNPs) approximately 70 nm in size were incorporated into a polyvinylidene fluoride (PVDF) matrix with different loadings (0–25 wt.%). The PVDF/h-BNNP nanocomposites were prepared by a solution blending technique and characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), polarized optical microscopy (POM) and scanning electron microscopy (SEM). In addition, the thermal conductivity and dielectric properties of the nanocomposites were investigated. The incorporation of h-BNNPs in the PVDF matrix resulted in enhanced thermal conductivity. The highest value, obtained at 25 wt.% h-BNNP loading, was 2.33 W/mK, which was five times that of the neat PVDF (0.41 W/mK). The thermal enhancement factor (TEF) at 5 wt.% h-BNNP loading was 78%, increasing to 468% at 25 wt.% h-BNNP loading. The maximum dielectric constant of approximately 36.37 (50Hz, 150 °C) was obtained at 25 wt.% h-BNNP loading, which was three times that of neat PVDF (11.94) at the same frequency and temperature. The aforementioned results suggest that these multifunctional and high-performance nanocomposites hold great promise for application in electronic encapsulation.     

Physicochemical Study of CPOL-701–Glass/Jute Composites

Glass and jute composites (CPOL-701-G and CPOL-701-J) have been fabricated by hand lay-up technique at 50°C under 27.6 MPa pressure for 3–4 h using MEKP and cobalt naphthenate. Both composites possess excellent tensile, flexural and dielectric strengths, volume resistivity and dielectric constant as well as hydrolytic stability against water, 10% aq. HCl and 10% aq. NaCl at 35°C. Cured CPOL-701 appears to be having good thermal stability (206°C) and high values of kinetic parameters. Excellent physicochemical properties of the composites signify their industrial importance.     

An Innovative Approach to the Synthesis of PMMA/PEG/Nanobifiller Filled Nanocomposites with Enhanced Mechanical and Thermal Properties

A facile route was adopted to blend the matrix. The PMMA/PEG blend was reinforced with three types of nanofillers, i.e., pristine MWCNT (P-CNT), amine functionalized MWCNT (PDA-EA-CNT) and nanobifiller i.e. nanodiamond functional MWCNT (PDA-EA-CNT-ND) to yield three different types of nanocomposites i.e. PMMA/PEG/P-CNT, PMMA/PEG/PDA-EA-CNT and PMMA/PEG/PDA-EA-CNT-ND. These nanocomposites were reinforced with nanofiller loading (1 wt. %, 3 wt. %, 5 wt. %, 10 wt. %, 30 wt. % and 50 wt. %) by solution casting method. Structure of composite and nanofillers was confirmed by FTIR. FESEM imaging revealed that nanocomposites have micro porous morphology. At high magnification, distribution of functionalized CNT/ND appears to be protruding out of the polymeric matrix. The TGA result suggests that the thermal stability of the nanocomposites was enhanced in comparison to PMMA due to grafting of filler molecules with PMMA/PEG macromolecules. The DTG results showed that the bifiller nanocomposites (PMMA/PEG/PDA-EA-CNT-ND) exhibited improved thermal stability with T_max (431^°C) as compared to P-CNT and amine functionalized CNT (PMMA/PEG/PDA-EA-CNT) with T_max of 395^°C and 418^°C respectively. XRD results showed fine interaction between filler and the polymeric matrix. As the filler loading was increased the composites showed pronounced XRD peak at 25.9^°, corresponding to (002) reflection of nanotubes. Significant improvement in the mechanical properties of composites was recorded with the reinforcement of fillers as compared to the neat matrix. The most significant improvement in tensile strength and elastic modulus was observed for the bifiller nanocomposites with 5 wt. % PDA-EA-CNT-ND. They showed a tensile strength and elastic modulus of 29.9 MPa and 1474.31 MPa respectively as compared to amine functionalized CNT with tensile strength (25.7) and elastic modulus (1466.99 MPa)and P-CNT with tensile strength(25 MPa) and elastic modulus (1155.75 MPa).     

Simultaneously improved actuated performance and mechanical strength of silicone elastomer by reduced graphene oxide encapsulated silicon dioxide

Herein, graphene oxide (GO)-encapsulated silica (SiO₂) hybrids (GO@SiO₂) were prepared via electrostatic self-assembly of the 3-aminopropyltriethoxysilane (APS)-modified SiO₂ and GO. The as-prepared GO@SiO₂ was introduced into polydimethylsiloxane (PDMS) elastomer to simultaneously increase the dielectric constant (k) and mechanical properties of PDMS. Then, the in situ thermal reduction of GO@SiO₂/PDMS composites was conducted at 180°C for 2 h to increase the interfacial polarizability of GO@SiO₂. As a result, the values of k at 1000 Hz are largely improved from 3.2 for PDMS to 13.3 for the reduced GO@SiO₂ (RGO@SiO₂)/PDMS elastomer. Meanwhile, the dielectric loss of the composites remains low (<0.2 at 1000 Hz). More importantly, the actuated strain at low electric field (5 kV/mm) obviously increases from 0.3% for pure PDMS to 2.59% for the composites with 60 phr of RGO@SiO₂, an eightfold increase in the actuated strain. In addition, both the tensile strength and elastic modulus are obviously improved by adding 60 phr of RGO@SiO₂, indicating a good reinforcing effect of RGO@SiO₂ on PDMS. Our goal is to develop a simple and effective way to improve the actuated performance and mechanical strength of the PDMS dielectric elastomer for its wider application.     

Influence of epoxy addition on the thermal,mechanical, and dielectrical properties of polycyanurate films

In the study, polycyanurate (PCN)/epoxy resin (ER) blends are prepared to enhance the physical properties of cyanate ester resins. The effects of curing schedule and blend composition on their thermal, mechanical, and dielectrical properties of cured PCN/epoxy blend films are examined. FTIR analysis of the cured blend films exhibits the expected cyanurate and oxazolidinone peaks in all blend compositions except the film thermally treated for 1 h in the presence of 1% phenol. TGA results show that the thermal stability decreases with epoxy content in the blend film. From SEM analyses, it is observed that all films have very dense, smooth, and bubble free surface without phase separation. For the pure PCN, the dielectric constants are found to be 3.54–5.91 in the range of 10^?1–10⁷ Hz between 20°C and 200°C. PCN/epoxy blends up to 50% epoxy resin show a good stability of dielectric constant in this frequency band for 200°C, which is close to the dielectric constant of the homopolymerized PCN. Beyond this percentage of epoxy resin, dielectric constants of PCN/epoxy blends greatly increase at low‐frequency region (0.1–10³ Hz) due to the interfacial polarization governed by Maxwell–Wagner–Sillars effect. POLYM. ENG. SCI., 58:820–829, 2018. © 2017 Society of Plastics Engineers     

Effects of the composition ratio,eosin addition,and γ irradiation on the dielectric properties of poly(vinyl alcohol)/glycogen blends

The dielectric relaxation spectra of various poly(vinyl alcohol) (PVA)/glycogen blends and irradiated blend samples with 70 wt % PVA content that were undoped and doped with eosin were measured in extended temperature (30–160°C) and frequency (1 kHz to 1 MHz) ranges. Dielectric relaxation spectroscopy separates different molecular groups of a repeating unit of a polymer with respect to the rate of its orientation dynamics. In the high‐temperature range (>100°C), the σ relaxation, which is associated with the hopping motion of ions in the disordered structure of the biopolymeric material, can be measured. The electric dipole moment and the activation energy of the glass‐transition temperature relaxation process were calculated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and dielectric properties of (Ba0.5Sr0.4Ca0.1)TiO3/polystyrene composites

Polymer composites with polystyrene (PS) as matrix and (Ba_0.5Sr_0.4Ca_0.1)TiO₃ (BSCT) as fillers are prepared by solution casting method. It is found that the dielectric constant of the prepared BSCT/PS composites increases with increasing filler content over the frequency range from 100 Hz to 500 MHz. And the dielectric properties of the composites show a good temperature independency over the range of ?30°C to 80°C. For the composite with 50 vol % filler content, the dielectric constant and dielectric loss are comparable with the literature values reported for other PS composites used for microwave substrate. Several theoretical models are used to compare with the experimental data of the dielectric constant of the composites. The microstructure and thermal properties of the composites were also studied. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41398.     

Dielectric behaviour and sulphur vulcanization of the crosslinked butyl (XL-50) rubber

Dielectric losses of XL-50 vulcanizates were measured at four different frequencies, viz. 500 Hz, 1.0 kHz, 5.0 kHz and 10.0 kHz. The influence of curing temperature (140°, 150° and 160°C) and curing time were also investigated. The cure characteristics were studied with the help of a Monsanto rheometer at 150°, 160° and 170°C. There exists a close relation between the dielectric losses and the state of cure of the sulphur vulcanization. Maximum dielectric loss has been observed at the optimum cure time. Dielectric loss decreases as the curing temperature decreases. Low frequency of measurement is always accompanied by high dielectric loss. Rheometric results have been correlated with the dielectric measurements.     

Calcium copper titanate/polyurethane composite films with high dielectric constant,low dielectric loss and super flexibility

Calcium copper titanate(CCTO)/polyurethane composite films with high dielectric constant, low dielectric loss and super flexibility were fabricated by incorporating CCTO ceramic powders into millable polyurethane elastomer (MPU) matrix using a rubber milling combined with hot compression molding method. The composite films show uniform microstructures and the dielectric constant is as high as 35.2 while the dielectric loss is only 0.041 when CCTO content reaches 40 vol% at 100 Hz and room temperature (RT). Moreover, it is important to note that this film has stable dielectric constant and dielectric loss in a relatively wide temperature range (from 0 °C to 70 °C), which is significantly import to the practice use of electronic devices based on CCTO composites. In addition, the flexibility of the film could be retained even when the CCTO content is up to 40 vol% and the elongation at break of this composite film is as high as 159.1%. Theoretical analysis indicates that the experimental data are in good conformity to the effective medium theory (EMT) model with a derived n = 0.21, suggesting more close association of the dielectric constant with the CCTO filler size and shape.     

Dielectric Behavior of Na0.5Bi0.5TiO3-Based Composites Incorporating Silver Particles

The dielectric properties of Na_0.5Bi_0.5TiO₃ (NBT) -based composites incorporating silver particles prepared by sintering at a low temperature of ∼900°C are reported. The dielectric constant increases with the amount of metal silver particles in the measured frequency range (150 Hz to 1 MHz), and could be enhanced up to ∼20 times higher than that of pure NBT ceramics, which was ascribed to the effective electric fields developed between the dispersed particles in the matrix and the percolation effect. Further investigation revealed that the dielectric constant of the composites has weak frequency and temperature dependence (−50°C to +50°C).     

Elaboration and dielectric property of modified PZT/epoxy nanocomposites

Composites of lead zirconate titanate (PZT) 50 nm nanoparticles and epoxy resins have been produced with various PZT contents from 0 to 20 wt%. The morphology and thermal properties of prepared composites were characterized using scanning electron microscopy and differential scanning calorimetry. The PZT nanoparticles were found to be well dispersed in the epoxy resin matrix. The glass transition temperature (T_g) value of the nanocomposites increases from 164 to 178°C with increasing the PZT weight fraction. The dielectric composites properties dependences were studied via a wide range of frequency from 10 Hz to 100 kHz. The dielectric constant of PZT/epoxy composite was increased from 5.56 to 6.29 (at f = 1 kHz, T = 30°C), respectively to the incorporated PZT amount, and these values are higher than that the dielectric constant of pure cured epoxy resin, ε = 4.86. POLYM. COMPOS., 37:455–461, 2016. © 2014 Society of Plastics Engineers     

Novel dielectric behaviors in PVDF‐based semiconductor composites

Composites of polyvinylidene fluoride (PVDF) filled with different conductive fillers as carbon black (CB), nickel (Ni), zinc (Zn), and tungsten (W), respectively, were prepared at same processing condition. The temperature dependence of dielectric behaviors of composites was studied at wide filler concentration and wide frequency ranges. Results show that there are giant dielectric constants as the concentration of filler is near the percolation threshold. The dielectric constants of all studied composites decrease slowly with increasing of frequency and rise gradually with increasing filler contents in the composites. Two relaxation peak regions of dielectric constant are observed from ?30 to 40°C and from 100 to 150°C, which can be attributed to the contribution of polar effect of PVDF. The CB filled PVDF (CB/PVDF) composites present a lower percolation threshold than other metallic‐filler filled PVDF composites. The maximal dielectric constant was found in the Ni filled PVDF (Ni/PVDF) composite. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation and characterization of graphene oxide/poly(vinyl alcohol) composite nanofibers via electrospinning

Graphene oxide (GO) was well dispersed in poly(vinyl alcohol) (PVA) diluted aqueous solution, and then the mixture was electrospun into GO/PVA composite nanofibers. Electron microscopy and Raman spectroscopy on the as‐prepared and calcined samples confirm the uniform distribution of GO sheets in the nanofibers. The thermal and mechanical properties of the nanofibers vary considerably with different GO filler contents. The decomposition temperatures of the GO/PVA composite nanofiber dropped by 38–50°C compared with pure PVA. A very small loading of 0.02 wt % GO increases the tensile strength of the nanofibers by 42 times. A porous 3D structure was realized by postcalcining nanofibers in H₂. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Polymethylmethacrylate grafting onto polyvinyl alcohol/modified feldspar composites: preparation,properties and structure characterization

The orthogonal experiment design methods were used to select the optimal conditions of preparation for modified feldspar via conventional wet method with silane coupling agent KH570. The optimum scheme was followed by: reaction time 1.5 h, modifier content 8 wt%, pulp density 12 wt%, reaction temperature 70 °C, respectively. Furthermore, polyvinyl alcohol (PVA)/modified feldspar composites were prepared with feldspar coated with silane coupling agent KH570 via solution method. To improve the water resistance of PVA-based composites, polymethylmethacrylate grafted onto PVA/modified feldspar composites (PMMA-g-PVA) was obtained by surface-initiated atom transfer radical polymerization (SI-ATRP). PVA/modified feldspar composites before and after SI-ATRP were characterized by X-ray photoelectron spectroscopy, thermal gravimetric analyzer, X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy, successively. The tensile performance and water resistance of PVA/modified feldspar composites were tested by mechanical test and contact angle, respectively. It was shown that 5 wt% of modified feldspar could significantly improve the tensile strength of PVA-based composites. Moreover, both thermal stability and hydrophobicity for PVA/modified feldspar composites were distinctly enhanced after SI-ATRP. In all, this study provided an effective and feasible method for optimizing interface performance and enhancing the water resistance of PVA-based composites.