Composite Films Research Articles

Dual-gradient MXene/AgNWs/Hollow-Fe3O4/CNF composite films for thermal management and electromagnetic shielding applications

With the increasing prevalence of electronic devices, there is a pressing need for composite films that offer both efficient thermal management and superior electromagnetic interference (EMI) shielding. To address this, we developed a novel composite film featuring a controllable conductive-magnetic dual-gradient structure, composed of cellulose nanofibers (CNF), MXene, silver nanowires (AgNWs), and hollow ferric oxide (Fe3O4). This film was fabricated using a straightforward, cost-effective layer-by-layer vacuum filtration method. Leveraging CNF as the matrix material endows the film with remarkable flexibility. The integration of 2D MXene, 1D AgNWs, and 0D hollow Fe3O4 significantly enhances the film's thermal conductivity through multidimensional particle interactions, achieving a maximum value of 2.92 W/mK. Additionally, the dual-gradient structure of the film-comprising a transition layer and a reflection layer-improves EMI shielding efficiency by balancing high EMI shielding effectiveness with low electromagnetic wave reflection. Specifically, for the dual-gradient configuration (MAF)-25-CNF, the absorption coefficient (A) of electromagnetic waves incident on the low conductivity side reaches 0.23, and the shielding effectiveness reaches 45.8 dB. These findings highlight the potential of MXene/AgNWs/Fe3O4/CNF composite films with a controllable conductive-magnetic dual-gradient structure for applications in electronics, electrical engineering, and wearable technologies.

A New Mechanism for the Inhibition of SA106 Gr.B Carbon Steel Corrosion by Nitrite in Alkaline Water.

The purpose of this study was to investigate the composition of oxide films formed on SA106 Gr.B carbon steel in nitrite solutions at 35 °C for 1000 h. The product of the reduction of nitrite during the corrosion inhibition process was also examined. The X-ray photoelectron spectroscopy results revealed that a thin Fe3O4 film was formed and ammonium ions were adsorbed on the outermost surface of the oxide film. The presence of ammonium ions was also demonstrated by ion chromatography. These results indicate that nitrites are reduced to ammonium ions, which in turn promotes the formation of the protective Fe3O4 film.

Multifunctional 1D/2D silver nanowires/MXene-based fabric strain sensors for emergency rescue

Abstract Monitoring the vital signs of the injured in accidents is crucial in emergency rescue process. Fabric-based sensing devices show a vast range of potential applications in wearable healthcare monitoring, human motion and thermal management due to their wearable flexibility and high sensitivity. Nevertheless, flexible electronic devices for both precise monitoring of health under low strain and motion under large strain are still a challenge in extremely harsh environment. Therefore, development of sensors with both high sensitivity and wide strain range remains a formidable challenge. Herein, a wearable flexible strain sensor with a one-dimensional/two-dimensional (1D/2D) composite conductive network was developed for healthcare and motion monitoring and thermal management by coating 1D silver nanowires (AgNWs) and 2D Ti3C2Tx MXene composite films on nylon/spandex blended knitted fabric (MANS). The MANS strain sensor can simultaneously achieve high sensitivity (gauge factor for up to 267), a wide range of detection (1–115%), excellent repeatability and cycling stability (1000 cycles). The sensor can be utilized for human health monitoring including heartbeat, pulse detection, breathing and various human motion. Moreover, the MANS sensor also has the electrical heating properties and voltage control temperature between 20-110 °C can achieved at low voltage. In addition, the MANS shows hydrophobicity with water contact angle of 137.1°. The MXene/AgNWs composite conductive layer with high sensitivity under low and large strains, electrical thermal conversion, and hydrophobicity has great potential for precisely monitoring health and motion of the injured in emergency rescue in harsh environment.

Asymmetric and mechanically enhanced MOF derived magnetic carbon-MXene/cellulose nanofiber films for electromagnetic interference shielding and electrothermal/photothermal conversion

The prosperity of wearable and microelectronic devices tremendously facilitates to exploit thin and flexible composite films with multifunction. Free-standing MXene films have aroused considerable interest in the fields of electromagnetic interference (EMI) shielding and thermal management because of brilliant electrical conductivity, distinctive layered architecture and remarkable localized surface plasmon resonance effect. Nevertheless, the inferior mechanical strength and potential performance degradation in humid environments seriously constrain their practical applications. In this regard, robust and multifunctional CoNi-MOF-74 derived magnetic carbon/cellulose nanofibers (CNF)-MXene/CNF composite films with Janus architecture were successfully constructed via two-step vacuum-assisted filtration technology. The rational arrangement of functional fillers effectively improves the impedance matching, promoting the incident electromagnetic waves to enter the films for consumption. Constructing double-layered structure could induce the generation of “absorption-reflection-reabsorption” dissipation manner, dramatically enhancing EMI shielding performance. The bi-layered magnetic carbon/CNF-MXene/CNF composite membranes (0.1 mm in thickness) realize a fascinating EMI shielding effectiveness of 68.86 dB and a superior absorption efficiency of 58.82 dB. Meanwhile, the brilliant conductivity and significant localized surface plasmon resonance effect of MXene/CNF layer endow the composite films with excellent electrothermal/photothermal conversion capability, greatly broadening application prospects. The steady temperature of the composite films is as high as 112.9 °C within 10 s under the low driven voltage of 3.0 V and the saturation temperature reaches up to 154.2 °C within 15 s at the light intensity of 1500 W/m2, respectively. Moreover, the plentiful hydrogen bonding interaction and compact interfacial combination jointly enable the composite films to possess robust mechanical flexibility, satisfying the demands in practice. This work supplies a prospective guidance for preparing flexible and multifunctional composite films with Janus architecture, revealing great application potential in wearable and microelectronic devices even under harsh conditions.

Influence of carbon content and irradiation modes on the antibiotic removal from water using VIS-activated TiO2/expanded graphite composite photocatalysts

TiO2/expanded graphite (TiO2/EG) composite films were applied to water treatment for sulfadiazine (SDZ) degradation in a continuous flat plate photochemical reactor. The films were synthesized by sol-gel method and deposited on borosilicate glass by airbrush spray coating technique, forming a TiO2/C heterojunction. Increasing the amount of carbon promoted more efficient photocatalytic removal of SDZ under simulated sunlight, which increased from 9.1% in the absence of carbon to 49.8% for the material containing 7.5% C. From the formation of the TiO2/C heterojunction, morphological modifications, changes in the electronic structure and reduction of the band gap energy were observed. Type-II heterojunction formation was observed. Foreground and background irradiation modes were investigated, and a possible photocatalytic mechanism was proposed. TiO2/7.5 %-EG exhibited the best photocatalytic performance, with the possibility of reuse. The films showed good reusability in the SDZ degradation over 4 photocatalytic cycles. The influence of irradiation modes and the role of oxidizing species were discussed. The results showed that TiO2/EG hybrid films are a promising alternative for practical photocatalytic applications under sunlight.

Room temperature self-healing and high gas barrier properties of elastomer composites incorporated with liquid metal

Flexible electronic devices require stretchable packaging materials that provide a hermetic seal. However, conventional soft materials often exhibit strong gas permeability, making it difficult to achieve stable operation, which requires films with high deformability, self-healing capability, and gas barrier functionality. In this study, a layer by layer (LBL) method was employed to uniformly coat a controllable thickness of liquid metal (LM) onto a designed and synthesized self-healing thermoplastic polyurethane (TPU) film, successfully developing a stretchable gas barrier film (TPU/LM) with high gas barrier properties. The designed polyurethane film significantly enhanced the adhesion of the liquid metal, effectively preventing leakage. The experimental results show that the water vapor transmission rate (WVTR) of the TPU/LM composite film with a thickness of 40 μm is 4.04g/(m2·day). Compared to the film without LM, the gas barrier performance has been improved by approximately 16 times. Additionally, there is a significant enhancement in nitrogen (N2) barrier, with a permeation rate reaching 4.0*10−17 cm3 cm/(cm2·s·Pa), effectively blocking the N2 permeation. This demonstrates the universality of the TPU/LM in gas barrier applications. Furthermore, the TPU/LM film also demonstrated excellent electromagnetic shielding effectiveness. The self-healing capability of the stretchable gas barrier film allows it to recover its initial gas barrier performance after mechanical damage. Humidity-sensitive resistors encapsulated with TPU/LM exhibited stable operation in both air and 90 % humidity environments, confirming the superior barrier properties of the TPU/LM. Generally, the developed TPU/LM is suitable for packaging applications in the next generation of flexible electronic devices.

Photodimerization-Triggered Photopolymerization of Triene Coordination Polymers Enables Macroscopic Photomechanical Movements.

Controlling the packing of olefinic molecules in crystals is essential for triggering solid-state [2 + 2] photocycloaddition reactions and the synthesis of photocontrolled smart materials. Herein, we report the stepwise photodimerization-triggered photopolymerization of two triene coordination polymers (CPs), {[Zn(2-BBA)2(tpeb)]·0.5CH3CN}n (1, 2-HBBA = 2-bromobenzoic acid, tpeb = 1,3,5-tri-4-pyridyl-1,2-ethenylbenzene) and {[Zn(3-BBA)2(tpeb)]·CH3CN)}n (2, 3-HBBA = 3-bromobenzoic acid). Upon irradiation with 420 nm light, each pair of closely packed and parallel olefinic bonds in 1 undergoes a [2 + 2] cycloaddition reaction, which connects two adjacent Z-shaped chains into a ladder-like coordination chain [Zn(2-BBA)2(bpbdpvpcb)0.5]n (1a, bpbdpvpcb = 1,3-bis(4-pyridyl)-2,4-bis(3,5-di(2-(4-pyridyl)vinyl)phenyl]cyclobutene) through single-crystal to single-crystal (SCSC) transformation. After photodimerization from 1 to 1a has occurred, the olefinic bonds that were initially distant are brought in close enough proximity to meet the requirements for a subsequent [2 + 2] cycloaddition reaction. Upon further light irradiation, the neighboring bpbdpvpcb ligands in 1a experience a SCSC photopolymerization based on [2 + 2] photocycloaddition and transform into poly-3b,4,5,5a,8b,9,10a-octahydro-4,5,9,10-tetrapyridyl-2,7-di(2-(4-pyridyl)vinyl)dicyclobuta[e,l]-pyren (poly-otpdpvdcbp). 2 showed similar structural changes under UV light illumination. Under light exposure, single crystals of 1 and 2 with different morphologies exhibit bending, cracking, and jumping photomechanical motions. The composite film (1-PVA) engineered by dispersing crystalline particles of 1 in poly(vinyl alcohol) (PVA) displays interesting light-wavelength-dependent photomechanical motions and can perform photodriven swimming on a liquid surface. This work provides a useful and promising approach to enable photodimerization of those photoinactive olefin pairs embedded in CPs and opens a new route to synthesize organic polymers by using olefinic CP platforms.

Enhancing the mechanical properties of polylactic acid (PLA) composite films using Pueraria lobata root microcrystalline cellulose

To enhance the mechanical properties of polylactic acid (PLA) material, the PLA-based composite films are prepared by using Pueraria lobata (Willd.) Ohwi root microcrystalline cellulose (PRMCC) treated with 3-aminopropyl triethoxysilane (KH550) silane coupling agent as the dispersed phase through solvent casting method. The effects of the concentrations of PRMCC and KH550 as well as the KH550 pretreating condition (ethanol concentration) on the tensile properties of PLA-based composite films are investigated. The PLA-based composite film treated with 5 wt% PRMCC and 18 wt% KH550 (pretreated by 90 % EtOH) exhibits the greatest performance. Its elongation at break value is detected to be 4.0 %, 1.6 times as large as that of pure PLA film. The water absorption of the as-prepared PLA-based composite film is reduced from 0.49 % of the unmodified PLA/PRMCC film to 0.12 %. Moreover, the modified PLA-based composite film has a hydrophobic surface and exhibits good thermal stability. Compared with pure PLA film, the modified PLA-based composite film exhibits improved UV shielding performance with acceptable transparency. Furthermore, after adding poly(butylene adipate-co-terephthalate) (PBAT) to the composite system, the elongation at break of the PLA-based composite film is up to 7.2 %. This research can provide theoretical guidance for enhancing the performance of PLA products.

Modified Chitosan-Based Coating/Packaging Composites with Enhanced Antibacterial, Antioxidant, and UV-Resistant Properties for Fresh Food Preservation.

Chitosan-based biomass packaging materials are a promising material for food preservation, but their limited solubility, antioxidant capacity, UV resistance, and mechanical properties severely restrict their application. In this study, we developed a novel chitosan-based coating/packaging composite (QCTO) using quaternary ammonium salt and tannic acid (TA)-modified chitosan (QCS-TA) and oxidized chitosan (OCS). The introduction of quaternary ammonium salt and TA effectively improves the water solubility and antibacterial, antioxidant, and UV-resistant properties of chitosan. The Schiff-base bond formed between OCS and QCS-TA, along with the TA-mediated multiple interactions, conferred the prepared composite film with good mechanical properties (69.9 MPa tensile strength) and gas barrier performance to water (14.3 g·h-1·m-2) and oxygen (3.5 g·mm·m-2·h-1). Meanwhile, the prepared QCTO composites demonstrate excellent biocompatibility and safety and are applied as coatings for strawberries and bananas as well as packaging films for mushrooms. These preservation experiments demonstrated that the prepared composites are able to effectively reduce weight loss, prevent microbial growth, maintain color, and significantly prolong the shelf life of fresh products (bananas, strawberries, and mushrooms extended shelf life by 6, 5, and 6 days, respectively). Therefore, the developed QCTO coating/packaging film shows great potential for applications in the field of food preservation and packaging.

Bi-functional flexible Ag2Se/Polyvinylidene fluoride composite films for thermal energy conversion and electromagnetic interference shielding by solution 3D printing

Developing bi-functional thermoelectric (TE) and electromagnetic interference (EMI) shielding materials is an effective way for the integrated electronic devices to face the accumulated thermal energy and complicated electromagnetic environment. Herein, flexible Ag2Se/polyvinylidene fluoride (Ag2Se/PVDF) composite films were successfully prepared through solution 3D printing and subsequent annealing treatment. As Ag2Se content increased, both the power factor and average total EMI shielding effectiveness (SET) were boosted. When the mass fraction of Ag2Se was 85 wt%, a power factor of 904.6 μW m−1K−2 at 360 K was achieved for the ASP-85 composite film. Meanwhile, this ASP-85 composite film shown the outstanding SET value of 56.1 dB at 52 μm thickness. Flexible Ag2Se/PVDF composite films displayed the excellent thermal energy conversion and EMI shielding capacity.

Performance Properties and Finite Element Modelling of Forest-Based Bionanomaterials/Activated Carbon Composite Film for Sustainable Future

Thanks to its highly crystalline structure and excellent thermal, optical, electrical and mechanical properties, carbon and its derivatives are considered the preferred reinforcement material in composites used in many industrial applications, especially in the forest and forest products sector, including oil, gas and aviation. Since hydroxyethyl cellulose (HEC) is a biopolymer, it has poor mechanical and thermal properties. These properties need to be strengthened with various additives. This study aims to improve the thermal and mechanical properties of hydroxyethyl cellulose by preparing hydroxyethyl cellulose/activated carbon (HEC/AC) composite materials. With this study, composites were obtained for the first time and their mechanical properties were examined using a 3D numerical modeling technique. The thermal stability of the prepared composite materials was investigated via thermal gravimetric analysis (TGA). The samples were heated from 30 °C to 750 °C with a heating rate of 10 °C/min under a nitrogen atmosphere and their masses were measured subsequently. The mechanical properties of the composites were investigated via the tensile test. The viscoelastic properties of the composite films were determined with dynamic mechanical thermal analyses (DMTA) and their morphologies were examined with scanning electron microscopy (SEM) images. According to the results, the best F3 sample (films containing 3 wt.% activated carbon) had an elastic modulus of 168.3 MPa, a thermal conductivity value of 0.068 W/mK, the maximum mass loss was at 328.20 °C and the initial storage modulus at 30 °C was 206.13 MPa. It was determined that the hydroxyethyl cellulose composite films containing 3 wt.% activated carbon revealed the optimum results in terms of both thermal conductivity and viscoelastic response and showed that the obtained composite films could be used in industrial applications where thermal conductivity was required.

Development of multilayer composite film based on protein‐polysaccharides with the addition of onion waste extracts and their impact on the shallot quality

AbstractAt present, multilayer composite film is attractive in the production of biodegradable films due to its essential film properties. The current study mainly focused on overcoming the problems of poor water barrier and mechanical strength observed in monolayer films (SA‐CMC and G/SA‐CMC) made from gluten (G), sodium alginate (SA), and carboxymethylcellulose (CMC). The film was developed with the addition of onion waste extracts (OWEs), primarily from peel and stalk, to enhance functional properties. The multilayer composite film consists of three layers: an outer layer made of G, an inner layer made of SA, CMC, and a middle layer made of G/SA‐CMC. The developed composite film exhibited improved physical properties (thickness: 0.348–0.629 mm and moisture: 20.889%–21.403%), mechanical properties (tensile strength: 21.943–20.640 MPa), and barrier properties (WVP: 0.212–0.516 g/m.s.Pa × 10−14) compared to monolayer films (SA‐CMC and G/SA‐CMC). The addition of OWEs enhanced the multilayer film's phenolic (20.076 and 36.175 mgGAE/g) and antioxidant activity (73.850% and 42.667%). The study found that the multilayer control film had minimal changes in weight loss (9.75% ± 0.18%) and firmness (6.68 ± 0.64 N) compared to OWEs‐added films (9.93% ± 0.49–10.02% ± 0.14% and 6.61 ± 0.37 to 6.64 ± 0.18 N). However, fresh‐peeled shallot onion packed with control film exhibited higher bacterial counts (6.70 ± 0.42 CFU/g) and yeast and mold counts (5.08 ± 0.20 CFU/g) than those packed with the OWEs‐added film (6.49 ± 0.28–6.56 ± 0.27 CFU/g and 4.75 ± 0.18–4.89 ± 0.21 CFU/g), indicating that OWEs protect the onions from microbial degradation. Overall, the multilayer control film (without OWEs) showed better results for storing the fresh‐peeled shallot onion at 4°C for 21 days.Highlights Onion waste extracts have potent high antioxidant and antimicrobial properties Multilayer film's physical, mechanical, barrier, and functional properties improved Addition of onion waste extracts increased the film's antimicrobial activity Control film showed a better effect for storing fresh‐peeled shallot onion Developed film can store fresh‐peeled shallot onion for 21 days at 4°C.

Structural, morphological, and chemical composition of ternary ZrHfN thin films deposited by reactive co-magnetron sputtering

This study focuses on a deposited ternary zirconium hafnium nitride (ZrHfN) thin film prepared using the reactive co-magnetron sputtering technique. The effect of the nitrogen (N2) flow rate on the films' structural, morphological, and chemical composition was investigated. The gracing-incidence X-ray diffraction (GIXRD) showed that all ZrHfN thin films exhibited a crystalline face-centered cubic structure with a strong (111) orientation. With increasing the N2 flow rate, the film's crystallography changed based on thermodynamic theory. The films demonstrated uniformity and homogeneity in their ternary nitride composition, as confirmed by transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDS) mapping and electron probe microanalyzer (EPMA). Chemical state analysis using X-ray photoelectron spectroscopy (XPS) indicated the presence of both nitride and oxynitride species in all samples. Notably, the atomic concentration of the main elements (Zr, Hf, and N) remained relatively stable over the controlled N2 flow rate range. However, the N2 flow rate played a crucial role in forming hafnium nitride and oxynitride chemical states, whereas it did not significantly influence the Zr phases, dominated by Zr oxides. Additionally, the hardness of the ternary ZrHfN thin films exhibited enhancement comparable to typical ternary nitrides.

Synergistic effects of starch and carrageenan from Kappaphycus alvarezii in composite film formation: Physicochemical and degradable properties

Rising concerns around plastic pollution from single-use plastic (SUPs), especially food packaging, have driven interest in sustainable alternatives. As such, algae biomass has gained attention for bioplastic production due to algae's rapid growth and abundant polysaccharides. This research focuses on extracting carrageenan from Kappaphycus alvarezii, extensively cultivated in Sabah, Malaysia, and utilizing it in combination with starch and glycerol to develop algae-based films. The physicochemical properties and degradation rate of these films were evaluated, revealing that the addition of carrageenan enhanced overall thermal stability meanwhile increasing water solubility, water content but reducing the degradation rate and swelling degree. This is primarily due to the crystalline structures of carrageenan, which provide a more rigid arrangement compared to the network of starch polymers. However, the incorporation of starch into the blends has enhanced the elongation and surface morphology, resulting in more balanced properties. Overall, these carrageenan films displayed impressive thermal, mechanical, and biodegradability characteristics, establishing their viability as substitutes for conventional plastics.

Preparation & characterization of polyvinyl alcohol/thymol blue composites gel and films for low radiation dosimetry

BackgroundExposure to low radiation has been indispensable due to it is necessity in radiography and it is induced potential effects in patients and radiology staff. Hence the measurement and detection became inevitable for radiation practitioners and the patients. The study aimed to present the synthesis of polyvinyl alcohol gel doped with Thymol Blue dye (PVA/TB) as gel and films for low radiation dosimetry. MethodThe polymer was prepared under controlled parameters (PVA 5%, temperature 80 °C, dopped with 0.01, 0.03, 0.05, 0.07, 0.09 mw of TB). The formed gel and films were irradiated with x-ray as: 0, 2, 4, 6, 8, 10 mGy. ResultsGel and films showed color quenching from yellow to light yellow as the radiation dose increased, as well as gradual significant (R2 = 0.97) reduction in optical density for all concentration (0.01, 0.02–0.09 mw of TB). The UV-spectroscope for (PVA/TB0.01mw) gel showed absorbance peaks at λ = 435, 326 and 279 nm, that decreased significantly (R2 = 0.97) as the radiation dose increases. And XRD for (PVA/TB0.01 mw) reveals the crystallinity of PVA at 2 thetas = 19.5° which increased to 40.5% at 10 mGy. FTIR revealed the chemical bonds with relevant intensities (CH (725.1–781 & 3030 cm−1), C – C (883.2 & 1170.6 cm−1), C – O (1063- 1096 cm−1), CH2 (1357.6 cm−1 wagging, 2879.2 cm−1 alkyl stretch), C = C (1623.8–1651.5 cm−1), C = O (1681.6–1683.6 cm−1), C – OH (3288 cm−1)) that decreased as the radiation dose increased and new radiogenic bonds at vibrational bands 1063–1096 cm−1 referring to C – O – C of Polysaccharide's pyranose and at 2125.1 cm−1 for C ≡ C alkenyl). ConclusionBoth forms of PVA/TB films and gel showed feasibility and applicability for radiation detection and measurement.

Inkjet‐Printed Flexible and Transparent Ti3C2Tx/TiO2 Composite Films: A Strategy for Photoelectrically Controllable Photocatalytic Degradation

The 2D Ti3C2Tx MXene has a large specific surface area, abundant functional groups, and low work function, which has potential in the field of photocatalytic materials. However, the manufacturing of controllable films with high photocatalytic properties and desirable transmittance is a challenging task. Herein, low‐cost, large‐scale, and rapid preparation of Ti3C2Tx/TiO2 flexible composite films have been successfully prepared by inkjet printing technology, which can be applied in complex and special environments, as well as in photoelectrically controllable places for photocatalytic performance. With the increase of the anatase TiO2, the transmittance of Ti3C2Tx/TiO2 films increases from 55.37% to 73.27% at 780 nm, corresponding to the square resistance of 1.112–206.496 kΩ sq−1 and the figure of merit of 0.48–0.005. When the amount of anatase TiO2 is 15%, the film has the best photocatalytic effect on methylene blue (MB) dye, reaching 68.94%. After five cycles of testing, the degradation efficiency of MB dye decreases by only 5.68%, showing that the film has good cycling stability. This work provides a new research direction for photoelectrically controllable photocatalytic degradation in complex and special environments.

Fabrication and Application of Tannin Double Quaternary Ammonium Salt/Polyvinyl Alcohol as Efficient Sterilization and Preservation Material for Food Packaging.

Food packaging films play a vital role in preserving and protecting food. The focus has gradually shifted to safety and sustainability in the preparation of functional food packaging materials. In this study, a bisquaternary ammonium salt of tannic acid (BQTA) was synthesized, and the bioplastics based on BQTA and polyvinyl alcohol (PVA) were created for packaging applications. The impact of BQTA on antibacterial effect, antioxidant capacity, opacity, ultraviolet (UV) protective activity, mechanical strength, thermal stability, and anti-fog of the resultant bioplastics was examined. In vitro antibacterial experiments confirmed that BQTA possesses excellent antimicrobial properties, and only a trace amount addition of BQTA in PVA composite film could inhibit about 100% of Escherichia coli and Staphylococcus aureus. Compared to BQTA/PVA bioplastics with pure PVA, the experiment findings demonstrate that BQTA/PVA bioplastics show strong antioxidant and UV protection action and the performance of fruit preservation. It also revealed a small improvement in thermal stability and tensile strength. The small water contact angle, even at low BQTA concentrations, gave BQTA/PVA bioplastics good anti-fog performance. Based on the findings, bioplastics of BQTA/PVA have the potential to be used to create packaging, and they can be applied as the second (inner) layer of the primary packaging to protect food freshness and nutrition due to their antioxidant activity and biocompatibility.

Effects of Film Mulching on Soil Quality, Garlic Yield, and Garlic Quality

To determine the optimal film management technique for garlic planting, this study aimed to investigate the effects of various film cover methods on soil quality and garlic yield in garlic cropping systems. To achieve these goals, trials with different film cover methods were conducted at the Jiangsu Academy of Agricultural Sciences in Nanjing. To investigate the impact of changes in soil quality and garlic yield, we set up four treatments： no film treatment （CK）, black polyethylene film treatment （HPE）, black poly（butylene- adipate-co-terephthalate） （PBAT） with straw composite film treatment （HSJ）, and white PBAT film treatment （BJ） in a garlic cropping system. Our results indicated that specific mulch coverings had a positive effect on both soil quality and garlic yield. The film cover treatments resulted in significant changes in soil physicochemical properties and bacterial and fungal biomasses and indirectly improved soil quality. Compared to that under the no film treatment, the BJ treatment boosted soil quality by 70%, with the most significant impact, followed by that under the HPE and HSJ treatments, with improvements of 52% and 36%. Random forest modeling indicated that soil organic matter and total nitrogen were the most important factors influencing soil quality. The different film covers significantly increased the diameter of garlic bulbs and single quality. The HSJ treatment exhibited the most significant increase in garlic yield, with 46%, 19%, and 6% improvement compared to that in the CK, HPE, and BJ treatments, respectively. Correlation analysis showed that soil quality under film cover was significantly correlated with the starch content of garlic bulbs, garlic diameter, and single quality. This study highlights that selecting the appropriate mulch film aids in the production of garlic and helps to develop farmland that produces both high-quality and high-yield crops.

Construction of ion/electron transfer multi-channels for the composite film electrode from GO and cellulose derived porous carbon in supercapacitor

Due to excellent flexibility and dispersibility, 2D graphene oxide (GO) is regarded as one of the prospective materials for preparing self-supporting electrode material. Nevertheless, the self-stacking characteristic of GO significantly restricts the ion transmission and accessibility in GO-based electrodes, especially in the direction perpendicular to the electrode surface. Herein, a novel composite film was fabricated from GO and 3D porous carbon (PC) through vacuum filtration combined with thermal reduction strategy. The combination of GO and PC not only avoids the self-stacking of GO, but also exposes more active sites for ions in the inner. A massive released nitrogen and oxygen-containing gases during the thermal reduction endows the reduced graphene oxide (RGO) with abundant porous and CC, which contributes to the energy storage in the direction perpendicular to the electrode surface. Besides, the high specific surface area of the prepared composite film is favorable for the storage and release of charge on the electrode surface. Benefiting from the above characteristics, the electrode assembled by the as-prepared film exhibits ultrahigh areal/volumetric specific capacitance in supercapacitor and ZIHCs (Zinc ion hybrid capacitors). This work provides a promising approach for the development of advanced self-supported electrode materials with desirable electrochemical properties.

Amphiphilic colloidal particles/Ca2+ reinforced edible agar nanocomposite film by multiple cross-linking/microphase separation strategies

The agar (AG) film exhibited poor mechanical and water-resistant properties which limited its application for food packaging. The structural modification of AG nanocomposite film greatly impacts their macroscopic properties. In this paper, edible AG nanocomposite films were achieved by incorporating colloidal particles based on conjugates of whey protein isolate (WPI) and alginate oligosaccharides (AOS) as the nanofiller to obtain the micro-phase separation structure and the multiple cross-linking network with the synergistic interactions of the Ca2+ crosslinking. Firstly, WPI-AOS colloidal particles were synthesized through the Wet-heating Maillard reaction. Good compatibility between WPI-AOS colloidal particles and AG was exhibited, resulting in improved mechanical and water-resistant properties of AG composite films. Compared to pure AG film, the tensile strength (TS) of the agar composite film with 10% WPI-AOS colloidal particles increased significantly to 81.87 MPa from 24.02 MPa, and the elongation at break (EAB) also improved to 46.25% from 18.65%. The moisture content (MC), water solubility (WS), and water vapor permeability (WVP) of the AG composite film decreased by 33.1%, 18.0%, and 22.4% respectively. In addition, the multiple cross-linking network hindered the relative sliding between the AG molecular chain, which resulted in improved thermal stability of the composite film. Using soft colloidal particles as nanofillers to fabricate edible films for improving their properties is an effective and promising strategy.