Hydrophobic Properties Research Articles

Harnessing Green Electricity from Food: A Split Black Gram-Based Triboelectric Nanogenerator for a Self-Powered Autonomous Lighting System and Portable Electronics.

Triboelectric nanogenerators (TENGs) represent a promising solution to mounting environmental concerns associated with battery disposal amid the escalating demand for portable electronics. However, prevailing TENG fabrication predominantly relies on nonbiodegradable, nonbiocompatible, and synthetic materials, posing a grave ecological threat. To mitigate this, there is a pressing need to develop eco-friendly and green TENGs leveraging sustainable, naturally occurring materials. This study pioneers the use of split black gram (SBG) as a tribo-positive material for TENGs. SBG's effectiveness as a tribo-positive material stems from its abundance of oxygen-containing functional groups, as confirmed by FTIR analysis, facilitating electron donation during the triboelectric process. SBG offers compelling advantages, including widespread availability, cost-effectiveness, biodegradability, and hydrophobic and adhesive properties due to its richness in starch and protein, positioning it as an optimal choice for eco-conscious TENG manufacturing. The fabrication process of an SBG-TENG is not only economical and facile but also solvent-free, requiring no specialized tools. Demonstrating commendable performance, the SBG-TENG achieves a maximum power density of 15.36 μW/cm2 at 1 MΩ, with an open circuit voltage of 84 V and short circuit current of 28 μA, comparable to recent studies. In practical applications, the SBG-TENG seamlessly integrates with LEDs and portable electronic devices via a full bridge rectifier, successfully powering them postcapacitor charging. Moreover, an autonomous lighting system is developed by embedding the SBG-TENG in a foot mat, enabling wireless light control through human stepping on the mat, introducing power-saving functionality for residential and office environments. In essence, the introduction of the SBG-TENG not only delivers cost-effectiveness but also minimizes the environmental impact by harnessing sustainable energy from food sources.

Long‐time high‐pressure processing of a patatin‐rich potato proteins isolate: impact on aggregation and surface properties

SummaryIn this study, a 4% (w/w) dispersion of a commercial patatin‐rich potato protein isolate (Po‐PI) was pressurised at 400 MPa up to 48 h at 20 °C. Protein aggregation induced by high‐pressure processing (HHP) was followed by dynamic light scattering, intrinsic fluorescence (in‐situ or ex‐situ) or SAXS analysis. Surface properties (surface hydrophobicity and interfacial properties) of the HHP‐induced aggregates were also investigated. A gradual dimer dissociation/protein unfolding was observed under pressure. Po‐PI exhibited a slow relaxation time under pressure. Long‐time HHP (>4 h) induced significant modification of the Po‐PI protein structure with partial non‐reversible unfolding. After 48 h of pressurisation at 400 MPa, large aggregates (160 nm) were obtained and a monomodal distribution in intensity and in number frequency was observed indicating a controlled aggregation. Up to 24 h of pressurisation at 400 MPa, intermediate states were obtained after high‐pressure release. SDS‐PAGE profiles showed that HHP‐induced aggregation of Po‐PI was driven by non‐covalent interactions. All high‐pressure processed dispersions displayed a higher surface hydrophobicity as compared to non‐treated Po‐PI. Po‐PI dispersion treated for 8 h at 400 MPa presented the lowest adsorption rate, the highest final surface tension and formed the most rigid interfacial film. Po‐PI showed resistance to moderate pressure levels (400 MPa) and long pressure application times were required to induce significant protein denaturation/aggregation (≥24 h) and to optimally modify its interfacial properties (8 h).

Enhancing Methane Gas Sensing through Defect Engineering in Ag-Ru Co-doped ZnO Nanorods.

Detection of leaks of flammable methane (CH4) gas in a timely manner can mitigate health, safety, and environmental risks. Zinc oxide (ZnO), a polar semiconductor with controllable surface defects, is a promising material for gas sensing. In this study, Ag-Ru co-doped into self-assembled ZnO nanorod arrays (ZnO NRs) was prepared by a one-step hydrothermal method. The Ag-Ru co-doped sample shows a good hydrophobic property as a result of its particular microstructure, which results in high humidity resistance. In addition, oxygen vacancy density significantly increased after Ag-Ru co-doping. Density functional theory (DFT) calculations revealed an exceptionally high charge density accumulated at the Ru sites and the formation of a localized strong electric field, which provides additional energy for the CH4 reaction with •O2- at the surface at room temperature. Optimized AgRu0.025-ZnO demonstrated an outstanding CH4 sensing performance, with a limit of detection (LOD) as low as 2.24 ppm under free-heat and free-light conditions. These findings suggest that introducing defects into the ZnO lattice, such as oxygen vacancies and localized ions, offers a promising approach to improving the gas sensing performance.

Utilizing Recycled Expanded Polystyrene Plastics to Stabilize Metal–Organic Frameworks for Heterogeneous Catalysis

Polystyrene plastics present significant environmental and human health threats due to their poor recyclability and degradability. However, leveraging their properties to enhance material performance stands out as one of the most effective strategies for mitigating these issues. Here, we have employed recycled expanded polystyrene plastics to manufacture metal–organic framework/expanded polystyrene plastic composites (MOF@EPP) using an adverse solvent precipitation method. This method simultaneously recycles EPPs and safeguards moisture-sensitive MOFs. Due to the exceptional hydrophobic properties of EPPs, HKUST−1@EPP can maintain structural integrity even when immersed in water for 30 days. This method is applicable to other moisture-sensitive MOFs, such as MOF−74(Zn) and MIL−53(Al). The HKUST−1@EPP composite also exhibits desirable heterogeneous catalytic activity in the Knoevenagel condensation reaction between benzaldehyde and acrylonitrile. The conversion rate can reach 94.9% within 4 h at 90 °C and does not exhibit a significant decrease even after six cycles, even in the presence of water. This study not only introduces a novel concept for recycling polystyrene plastics, but also offers a practical strategy for safeguarding moisture-sensitive MOFs.

A Tunable Hydrophilic-Hydrophobic, Stimulus Responsive, and Robust Iridescent Structural Color Bionic Film with Chiral Photonic Crystal Nanointerface.

Bio-inspired in nature, using nanomaterials to fabricate the vivid bionic structural color and intelligent stimulus responsive interface as smart skin or optical devices are widely concerned and remain a huge challenge. Here, the bionic flexible film is designed and fabricated with chiral nanointerface and tunable hydrophilic-hydrophobic by the ultrasonic energy perturbation strategy and crosslinking of the cellulose nanocrystals (CNC). An intelligent nanointerface with adjustable hydrophilic and hydrophobic properties is constructed by the supramolecular assembly using a smart ionic liquid molecule. The bionic flexible film possessed the variable hydrophilic-hydrophobic, stimulus responsive, and robust iridescent structural color. The reflective wavelength and the helical pitch of the film can be easily modulated through the ultrasonic energy perturbation strategy. The bionic flexible film by covalent cross-linking has excellent robustness, good elasticity and flexibility. The tunable brilliant structural color of the chiral nanointerface is attributed to the surface charge change of the CNC photonic crystal, which is disturbed by ultrasonic energy perturbation. The bionic flexible film with tunable structure color has intelligent hydrophilic and hydrophobic stimulus response properties. The chiral bionic materials have potential applications in smart skin, optical devices, bionic materials, robots, anti-counterfeiting, colorful displays, and stealth materials.

A novel potentiometric screen-printed electrode based on crown ethers/nano manganese oxide/Nafion composite for trace level determination of copper ion in biological fluids.

Copper levels in biological fluids are associated with Wilson's, Alzheimer's, Menke's, and Parkinson's diseases, making them good biochemical markers for these diseases. This study introduces a miniaturized screen-printed electrode (SPE) for the potentiometric determination of copper(II) in some biological fluids. Manganese(III) oxide nanoparticles (Mn2O3-NPs), dispersed in Nafion, are drop-casted onto a graphite/PET substrate, serving as the ion-to-electron transducer material. The solid-contact material is then covered by a selective polyvinyl chloride (PVC) membrane incorporated with 18-crown-6 as a neutral ion carrier for the selective determination of copper(II) ions. The proposed electrode exhibits a Nernstian response with a slope of 30.2 ± 0.3mV/decade (R2 = 0.999) over the linear concentration range 5.2 × 10-9 - 6.2 × 10-3mol/l and a detection limit of 1.1 × 10-9mol/l (69.9ng/l). Short-term potential stability is evaluated using constant current chronopotentiometry (CP) and electrochemical impedance spectroscopy (EIS). A significant improvement in the electrode capacitance (91.5 μF) is displayed due to the use of Mn2O3-NPs as a solid contact. The presence of Nafion, with its high hydrophobicity properties, eliminates the formation of the thin water layer, facilitating the ion-to-electron transduction between the sensing membrane and the conducting substrate. Additionally, it enhances the adhesion of the polymeric sensing membrane to the solid-contact material, preventing membrane delamination and increasingthe electrode's lifespan. The high selectivity, sensitivity, and potential stability of the proposed miniaturized electrode suggests its use for the determination of copper(II) ions in human blood serum and milk samples. The results obtained agree fairly well with data obtained by flameless atomic absorption spectrometry.

A high-efficiency clay mineral based organic photocatalyst towards photodegradation of butyl xanthate in mineral processing wastewater

The organic solar cell active layer, well known for excellent visible light response capability, is regarded as a potential candidate for photocatalytic degradation of organic wastewater. However, the poor dispersibility in water due to its hydrophobicity property severely limited the degrading efficiency. In this work, a novel composite photocatalyst PM6:IDT8CN-M/CK2 with a broad visible absorption spectrum and non-toxicity was first synthesized through the intercalation compounding method. A good dispersibility of PM6:IDT8CN-M in wastewater was achieved with the help of rich interlamellar porosity and good hydrophilicity of calcined kaolin. This composite photocatalyst was successfully applied to the SBX photocatalytic degradation in mineral processing wastewater, and the SBX pollutants can be completely degraded within 10 min under the condition of visible light irradiation. Compared with other reported photocatalysts, the photocatalytic degradation efficiency of SBX was dramatically improved by at least seven times. Moreover, PM6:IDT8CN-M/CK2 has remarkable stability, sustaining degradation efficiencies of over 90 % in 60 cycles. Notably, the organic solar cell active layer in PM6:IDT8CN-M/CK2 can achieve carrier rapid separation and transport, enhancing the generation of active oxides (∙O2–, and ∙OH, etc.). At the same time, the large surface area of PM6:IDT8CN-M/CK2 provides a suitable environment for the oxidation reaction of active radicals with SBX to achieve this efficient photocatalytic degradation. Overall, this work not only extends the application scope of organic solar cell active layer, but also develops a high-efficiency SBX removal technique for the treatment of mineral processing wastewater.

Continuous preparation and antibacterial mechanisms of biodegradable polylactic acid/nano-zinc oxide/additives antibacterial non-wovens

Biodegradable polylactic acid (PLA)/nano‑zinc oxide (ZnO)/additives non-woven slices were prepared by melt blending method. The effects of antibacterial agent nano-ZnO, antioxidant pentaerythrityl tetrakis-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate (1010), and chain extender multi-functional epoxy (ADR), on the melt flow rate, mechanical properties, thermal stabilities and micromorphology of the slices were investigated. The melt flow rate decreased from 26.94 g/10 min to 17.76 g/10 min, and the tensile strength increased from 10.518 MPa to 30.427 MPa with the increase of nano-ZnO and additives content. The slices were further spunbonded. The wettability and antibacterial properties of PLA/nano-ZnO/additives antibacterial non-wovens were studied, and the antibacterial action mechanism was clarified. The results showed that the biodegradable PLA/nano-ZnO/additives antibacterial non-wovens were prepared continuously successfully. The prepared non-woven fabrics exhibited good hydrophobicity and antibacterial properties. The mechanism study shows that zinc ion produced by nano-ZnO and photocatalytic reaction make the fabrics have good antibacterial activity at low nano-ZnO content. When nano-ZnO concentration reaches 1.5 wt%, the antibacterial rate against Escherichia coli and Staphylococcus aureus reaches 98.52 % and 98.13 %, respectively.

A Tape-Wrapping Strategy towards Electrochemical Fabrication of Water-Dispersible Graphene.

Graphene has achieved mass production via various preparative routes and demonstrated its uniqueness in many application fields for its intrinsically high electron mobility and thermal conductivity. However, graphene faces limitations in assembling macroscopic structures because of its hydrophobic property. Therefore, balancing high crystal quality and good aqueous dispersibility is of great importance in practical applications. Herein, we propose a tape-wrapping strategy to electrochemically fabricate water-dispersible graphene (w-Gr) with both excellent dispersibility (~4.5 mg/mL, stable over 2 months), and well-preserved crystalline structure. A large production rate (4.5 mg/min, six times faster than previous electrochemical methods), high yield (65.4% ≤5 atomic layers) and good processability are demonstrated. A mechanism investigation indicates that the rational design of anode configuration to ensure proper oxidation, deep exfoliation and unobstructed mass transfer is responsible for the high efficiency of this strategy. This simple yet efficient electrochemical method is expected to promote the scalable preparation and applications of graphene.

Fabrication of hydrophobic surface from zein-based nanostructure and rosin to functionalize cotton textiles

A double-layer hydrophobic coating based on zein nanoparticles (ZNPs) and rosin was successfully developed as a simple and non-toxic process for textile functionalization. The bottom layer of the coating was a highly rough surface formed by the accumulation of zein nanoparticles prepared with an antisolvent method. The top layer was made of rosin to reduce the surface energy. The fabric treated with ZNPs and rosin (ZNPs/R/cotton) exhibited good hydrophobic behavior with a water contact angle (WCA) of 131.5 ± 2.3° and the hydrophobicity was long-lasting. The micromorphology and chemical composition of hydrophobic cotton fabric surface were characterized by scanning electron microscopy (SEM) and infrared spectroscopy (FTIR), respectively. The results demonstrated that zein and rosin deposited on the surface of the fabric to form a rough micro/nano-scale structure. The functional ZNPs/R/cotton retained excellent mechanical properties, air permeability and water vapor permeability. The practical application tests indicated that the fabric displayed good stain resistance ability. Even after 10 soaking cycles and 50 rubbing cycles, the fabric still retained good hydrophobic property with WCAs of 124.7 ± 2.9° and 90.3 ± 3.5°. This work offered a potential method for the clean production of functionalized textiles.

Expanded polystyrene waste valorization as a hydrophobic coating II: packaging application

The application of the expanded polystyrene (EPS) waste to the functional material is still a challenge. The hydrophobic property of polystyrene has a potential to create a superhydrophobic surface. Here, we use expanded polystyrene waste to coat surfaces in two different ways—spray coating and dip coating—to produce superhydrophobic surfaces for food packaging. The ZnO was employed to make the surface rougher. However, the combination of ZnO and EPS waste produces only a hydrophobic surface. For spray coating and dip coating, the maximum water contact angle is 119° and 125° respectively. The scanning electron microscope (SEM) picture reveals many holes that increase the surface's roughness. The hydrophobic surface significantly cuts down on cleaning time. According to the food packaging parameter test mandated by the Indonesian Food and Drug Administration (BPOM) (BPOM regulation No. 20, 2019), the coating complies with heavy metals and ethanol stimulant migration testing requirements for food packaging. However, the migration condition in acetic acid stimulant surpasses the maximum standard. The total migration in 3% acetic acid stimulant (40°C for 10 days) is 22.95 mg/dm2 while the maximum value is 10 mg/dm2.

Investigations on the Impact of a Series of Alkoxysilane Precursors on the Structure, Morphology and Wettability of an Established Zirconium-Modified Hybrid Anticorrosion Sol–Gel Coating

Investigations on the Impact of a Series of Alkoxysilane Precursors on the Structure, Morphology and Wettability of an Established Zirconium-Modified Hybrid Anticorrosion Sol–Gel Coating

Space confinement effect of carbon nanotube-alumina strip support on the Cu-Co catalysts for CO2 methanation

The present work reported the space confinement effect of carbon nanotube-alumina strip (CAS) support on the Cu-Co bimetallic catalyst or the single Cu, Co catalysts for the CO2 methanation. CAS, made by extrusion of nanotubes and Al-based sol and high temperature calcination, was a macroscopic support with sufficient mesopores and hydrophobic property. Cu-Co/CAS catalysts exhibited high catalytic activity for methanation of CO2 (H2/CO2=3:1), where CO2 conversion was 49.62% and CH4 selectivity was 95.98% at temperature as low as 250 ℃ and 1.5 MPa, and showed advantage significantly over those with the supports of individual nanotube or pure Alumina support. The comparison suggested the hydrophobicity of carbon nanotubes can effectively remove water from the metal active sites, enhancing the equilibrium of reverse water gas shift and CO methanation reactions, as compared to alumina support. Additionally, CAS support had a spatial confinement effect that increased the contact time of CO2 or intermediates with the active sites, compared with individual nanotube support. XPS and Raman spectroscopy validated the presence of oxygen vacancies of CAS, promoting the CO2 methanation. H2-TPR results, in combination with DFT calculations, confirmed that the CAS supports enabled the Cu-Co active phase by changing their electronic structures, to possess a strong adsorption activation capacity for H2 at low temperatures with high performance for CO2 methanation.

Titanate-grafted carbon black-facilitated MPLs for advanced proton exchange membrane fuel cells

This study introduces a novel hydrophobic modification for microporous layers (MPLs) in proton exchange membrane fuel cells (PEMFCs), utilizing a chemical grafting method with Titanate coupling agent NDZ-201 on carbon black. This method overcomes the drawbacks of traditional MPLs that use polytetrafluoroethylene (PTFE) and require high-temperature post-processing, which can lead to pore blockage. The treated carbon black exhibits outstanding hydrophobic properties, enhancing both water and gas flow through the cell, thereby significantly boosting its electrochemical capabilities. With an ideal carbon loading of 2 mg cm⁻² for MPL, the cell delivers an impressive peak power density of 1045.8 mW cm⁻². The treatment also increases the contact angle of the carbon black from 65° to 156°, achieving superhydrophobicity through covalent bonding with NDZ-201. This fluorine-free, covalent grafting approach presents a new method for the development of MPLs for PEMFCs, facilitating performance improvement and sustainability. The study highlights the significance of the intricate interplay among various factors, including chemical grafting for hydrophobicity, carbon loading and open pores, affecting fuel cell performance.

Efficient Carbon‐Based Hole‐Conductor‐Free Printable Mesoscopic Perovskite Solar Cells via a Multifunctional Fluorinated Molecule

AbstractBenefiting from their simple and cost‐effective fabrication procedures, printable mesoscopic perovskite solar cells (p‐MPSCs) exhibit substantial potential for large‐scale production. In p‐MPSCs, the thickness of the perovskite filled in the TiO2 and ZrO2 mesoporous layers is ≈3 µm. Therefore, the perovskite crystallization process is more intricate and challenging in the mesoporous structure than the general planar thin film (0.3–0.5 µm). In this work, a multifunctional fluorinated molecule is applied to work as an additive to improve the perovskite crystallization, enhance the device efficiency, and elevate the operational stability. This additive forms robust coordination between its carbonyl groups and uncoordinated Pb2+, thereby effectively passivating defects. The hydrophobic properties of the fluorinated molecule contribute to the device's water‐resistant capability and long‐term operational stability. With these synergistic effects, the power conversion efficiency (PCE) of small‐area cells (0.1 cm2) reaches 20.15% under 1 sun illumination. Large‐area modules (56.4 cm2) are fabricated and exhibit a PCE of 15.41%.

A thermodynamic theory coupling photo-chemo-mechano interactions for light-responsive hydrogel

Light-responsive hydrogel, as a typical functional hydrogel, is composed of crosslinked hydrophilic polymer chains, photosensitive molecules and water. Under illumination, the photosensitive molecules exhibit a transition in hydrophilic/ hydrophobic properties, leading to migration of water molecules and deformation of the hydrogel based on the temporal and spatial distribution of light. In this study, we propose a nonequilibrium thermodynamic framework to study the photo-chemo-mechano behaviors of light-responsive hydrogel. We firstly describe the light propagation in the hydrogel and the photochemical reaction kinetics. New free energy functions to expound the relationship between the photochemical reaction and thermodynamic process are established, and the constitutive equations are derived. Subsequently, we implant the model into a multi-field coupling analysis software, COMSOL, to conduct a spatio-temporal analysis of the hydrogel's response under uniform light exposure. Finally, we simulate the inhomogeneous deformation of light-responsive hydrogel strips under different illumination conditions and compare the results with experiments. The results highlight the importance of the photochemical reaction rate and the redistribution of light field caused by deformation. The present research holds potential for the precise manipulation and optimal design of light-responsive hydrogel in prospective applications, and offers insights for the synthesis of similar materials as well as the design of pertinent devices.

Investigation on production and reaction conditions of sucrose synthase based glucosylation cascade towards flavonoid modification

Enzyme-based glycosylation is of great interest in the context of natural products decoration. Yet, its industrial application is hindered by optimisation difficulties and hard-to-standardise productivities. In this study, five sugar nucleotide-dependent glucosyltransferases from different origins (bacterial, plant and fungal) were coupled with soy sucrose synthase (GmSuSy) to create a set of diverse cascade biocatalysts for flavonoid glucosylation, which evaluation brought new insights into the field. Investigations into co-expression conditions and reaction settings enabled to define optimal induction temperature (25 °C) and uridine diphosphate (UDP) concentration (0.5 mM) for all tested pairs of enzymes. Moreover, the influence of pH and substrate concentration on the monoglucosylated product distribution was detected and analysed. The utilisation of crude protein extracts as a cost-effective source of catalysts unveiled their glycosidase activity against flavonoid glucosides, resulting in decreased productivity, which, to our knowledge, has not previously been discussed in such a context. Additionally, examination of the commercially available EziG immobilisation resins showed that selection of suitable carrier for solid catalyst production can be problematic and not only enzyme’s but also reagent’s properties have to be considered. Flavonoids, due to their complexation and hydrophobic properties, can adsorb on different types of surfaces, including divalent metal ions required for IMAC based immobilisation, necessitating detailed examination of the resins while the catalysis design.

Engineered polymer nanoparticles as artificial chaperones facilitating the selective refolding of denatured enzymes

Molecular chaperones assist in protein refolding by selectively binding to proteins in their nonnative states. Despite progress in creating artificial chaperones, these designs often have a limited range of substrates they can work with. In this paper, we present molecularly imprinted flexible polymer nanoparticles (nanoMIPs) designed as customizable biomimetic chaperones. We used model proteins such as cytochrome c, laccase, and lipase to screen polymeric monomers and identify the most effective formulations, offering tunable charge and hydrophobic properties. Utilizing a dispersed phase imprinting approach, we employed magnetic beads modified with destabilized whole-protein as solid-phase templates. This process involves medium exchange facilitated by magnetic pulldowns, resulting in the synthesis of nanoMIPs featuring imprinted sites that effectively mimic chaperone cavities. These nanoMIPs were able to selectively refold denatured enzymes, achieving up to 86.7% recovery of their activity, significantly outperforming control samples. Mechanistic studies confirmed that nanoMIPs preferentially bind denatured rather than native enzymes, mimicking natural chaperone interactions. Multifaceted analyses support the functionality of nanoMIPs, which emulate the protective roles of chaperones by selectively engaging with denatured proteins to inhibit aggregation and facilitate refolding. This approach shows promise for widespread use in protein recovery within biocatalysis and biomedicine.

Preparation of fluorinated polysiloxane and its application in modified polyacrylates

AbstractPolyacrylate materials are widely used in textile adhesives, functional finishing agents, architectural coatings, and other fields. In order to improve their hydrophobicity and flexibility, a novel fluorinated polysiloxane was prepared by acid catalyzed bulk ring opening reaction with octamethylcyclotetrasiloxane (D4), tetramethyltetravinylcyclotetrasiloxane (), and methyltrifluoropropylcyclotrisiloxane (), and its structure was characterized. Then, as a modified monomer, the fluorinated polysiloxane modified polyacrylates was prepared by miniemulsion polymerization. The effects of fluorinated polysiloxane monomers with different vinyl content and molecular weight on the properties of emulsion, film structure and film hydrophobicity were studied. The results showed that when using fluorinated polysiloxane monomer with Mn = 6235, vinyl content of 0.33 mmol/g, and fluorine content of 7.40 mmol/g for modification, the water contact angle on the surface of the adhesive film reached 100.4°, and the water absorption rate was 8.1%, resulting in the best effect. Used for textile printing, the color fastness to dry and wet friction after fabric printing could reach level 4, and the hand feel was soft.

Effect of post-heat treatment on the UV transmittance, hydrophobicity, and tensile properties of PVA/Uncaria gambir extract blend films

The physical and mechanical properties of biopolymers can be improved by heating technologies. In this research, we improved the properties of Polyvinyl alcohol (PVA)/Uncaria gambir extract (UGE) blend films by post-heating method. After post-heating, the blend film exhibited higher resistance to UV light and improved contact angle performance, while water vapor permeability and moisture absorption decreased. The tensile strength and toughness of the PVA/UGE blend film with a post-heating duration of 40 min were 68.8 MPa and 57.7 MPa, respectively, an increase of 131 % and 127 %, compared to films without post-heating. This facile and cost-effective fabrication method, with environmentally friendly properties, can be applied to biodegradable PVA/UGE blend films to achieve desired properties for optical devices or food packaging materials.