Cellulose Composite Films Research Articles

Preparation of pectin/carboxymethyl cellulose composite films via high-pressure processing and enhancement of antimicrobial packaging

This study investigated the impact of high-pressure processing (HPP) treatment on the structure and physicochemical properties of pectin (PEC)/carboxymethyl cellulose (CMC) composite films, along with the development of new active films incorporating emodin as an antibacterial agent. The results showed that 500 MPa/20 min HPP treatment significantly improved the tensile strength (from 45.91 ± 4.63 MPa to 52.24 ± 4.87 MPa) and elongation at the break (from 5.00 ± 1.44 % to 11.72 ± 2.97 %) of the films. It also improved the film's thermal stability and had no significant effect on its thermal degradability. Moreover, emodin was incorporated into the PEC/CMC film-forming solution and subjected to 500 MPa/20 min HPP treatment to investigate the structure, functional properties, optical properties, and antibacterial activity of the film. The emodin caused the film structural alteration, but significantly improved the water vapor barrier properties. It also reduced the film brightness and light transmission. The antibacterial assessment demonstrated that the film's antibacterial activity was correlated positively with increasing emodin content, and the number of viable cells of Staphylococcus aureus decreased by 1.29 log10 CFU/mL, 1.70 log10 CFU/mL, and 1.80 log10 CFU/mL with different levels of EM antimicrobial films after 12 h.

Photon upconversion crystals doped bacterial cellulose composite films as recyclable photonic bioplastics

Biopolymers currently utilized as substitutes for synthetic polymers in photonics applications are predominantly confined to linear optical color responses. Herein we expand their applications in non-linear optics by integrating with triplet-triplet annihilation photon upconversion crystals. A photon upconverting biomaterial is prepared by cultivating Pd(II) meso-tetraphenyl tetrabenzoporphine: 9,10-diphenyl anthracene (sensitizer: annihilator) crystals on bacterial cellulose hydrogel that serves both as host and template for the crystallization of photon upconversion chromophores. Coating with gelatin improves the material’s optical transparency by adjusting the refractive indices. The prepared material shows an upconversion of 633 nm red light to 443 nm blue light, indicated by quadratic to linear dependence on excitation power density (non-linearly). Notably, components of this material are physically dis-assembled to retrieve 66 ± 1% of annihilator, at the end of life. Whereas, the residual clean biomass is subjected to biodegradation, showcasing the sustainability of the developed photonics material.

Agar/carboxymethyl cellulose composite film loaded with hydroxyapatite nanoparticles for bone regeneration

Agar/carboxymethyl cellulose composite film loaded with hydroxyapatite nanoparticles for bone regeneration

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.

In situ growth of curcumin-loaded cellulose composite film for real-time monitoring of food freshness in smart packaging

Visual pH-responsive packaging material is particularly important in food supply chain safety monitoring due to their non-destructive monitoring method and intuitive result. However, it has always been limited by the instability performance of pH-response components and carriers, which further hinders its wide food safety application. To address these challenges, we selected cellulose with remarkable biocompatibility and mechanical properties as the carrier, and high pH-responsive curcumin to develop a smart packaging material (RC/GC composite film) with real-time food safety monitoring. Compared with pure cellulose film, the RC/GC composite film exhibited excellent mechanical properties (4-fold enhancement) and thermal stability (100 °C increasing). Meanwhile, based on the first reported strategy of curcumin in-situ growth during cellulose film formation, the RC/GC composite film exhibited exceptional antioxidant activity (89.2 %), antimicrobial property (91.6 %), and significant pH-responsive sensitivity (within 15 s). This innovative approach offers a new strategy for easy-to-use and effective monitoring of food spoilage in packaging materials.

Waste cotton textile-derived cellulose composite porous film with enhanced piezoelectric performance for energy harvesting and self-powered sensing

Integrating flexible piezoelectric nanogenerators (PENGs) into wearable and portable electronics offers promising prospects for motion monitoring. However, it remains a significant challenge to develop environmentally friendly PENGs using biodegradable and cost-effective natural polymers for mechanical energy harvesting and self-powered sensing. Herein, reduced graphene oxide (rGO) and barium titanate (BTO) were introduced into regenerated cellulose pulp to fabricate a composite porous film-based PENG. The incorporation of rGO not only increased the electrical conductivity of the porous film but also enhanced the dispersibility of BTO. Moreover, the unique pore structure of the composite porous film improved the polarization effect of the air inside the pores, thereby greatly boosting the overall piezoelectric performance. The piezoelectric coefficient of the resulting composite porous film reaches up to 41.5 pC·N−1, which is comparable to or higher than those reported in similar studies. Consequently, the PENG assembled from this cellulose/rGO/BTO composite porous film (CGB-PENG) achieved an output voltage of 47 V, a current of 4.6 μA, and a power density of 30 μW·cm−2, approximately three times the output voltage and ten times the power density of similar studies. This work presents a feasible approach for the fabrication of high-performance cellulose-based PENGs derived from recycled waste cotton textiles.

Development and characterization of pomegranate peel extract-infused carboxymethyl cellulose composite films for functional, sustainable food packaging

Our study explores the development and characterization of carboxymethyl cellulose (CMC)-based composite films integrated with clay particles and pomegranate peel extract (PE), aiming to inspire the films with natural antimicrobial and antioxidant properties for potential applications in food packaging. We conducted a comprehensive examination of the mechanical, barrier, surface, and degradation properties of these composite films, considering the impacts of incorporating clay particles and PE on their overall performance. Our findings reveal that the inclusion of clay particles enhances the mechanical strength and barrier properties of the films, while PE contributes to antioxidant and antibacterial effects. Namely, after the integration of 3 wt% clay, the tensile strength exhibited a remarkable increase of approximately 300%, accompanied by a notable reduction of 60% in water vapor permeability and 30% in oxygen transmission rate. Furthermore, the integration of PE into CMC films promoted antibacterial activity against 2 g-positive bacterial species, Staphylococcus aureus and Listeria monocytogenes. Additionally, we conducted a life cycle assessment (LCA) to quantify the cradle-to-gate environmental impacts of the developed bio-based active films. When normalized to the functional properties of the films, including mechanical and barrier performance, we observed significant benefits, with reductions of up to 59% after the concurrent incorporation of PE and clay nanosheets. Overall, our study underscores the potential of CMC-based composite films augmented with PE as a promising solution for sustainable food packaging, offering enhanced functionality while reducing environmental impact and increasing food safety.

The study of citric acid crosslinked β-cyclodextrin/hydroxypropyl cellulose food preservation film

Abstract In this study, hydroxypropyl cellulose (HPC) was utilized as the raw material, with the addition of β-cyclodextrin (β-CD), citric acid (CA) as the crosslinking agent, and sodium hypophosphite (SHP) as the catalyst to produce hydroxypropyl cellulose/β-CD composite films. The inclusion of β-CD resulted in an increase in the tensile strength of the film, with the maximum value of 13.5 MPa for the 1 % β-CD composite membrane. Additionally, after degradation in soil for 28 days, the degradation ability was significantly enhanced, with the 1.0 % β-CD composite film exhibiting the highest degradation rate of 27.21 %. Furthermore, the water permeability of the composite membrane was improved with the addition of β-CD. Specifically, when the β-CD content was 1.0 %, the water vapor transmission reached its lowest point at 2,445 g* ( m 2 * 24 d ) − 1 ${({m}^{2}\ast 24d)}^{-1}$ . The findings demonstrated that the 1 % β-cyclodextrin/hydroxypropyl cellulose composite film effectively preserved the freshness of strawberries, reducing the weight loss rate by 1.65 % compared to the control group. In conclusion, this research highlights the potential for preparing composite membranes using HPC and β-CD crosslinking, thereby expanding the application of hydroxypropyl cellulose and β-CD in food preservation.

Tough and Elastic Cellulose Composite Hydrogels/Films for Flexible Wearable Sensors.

Cellulose and its composites, despite being abundant and sustainable, are typically brittle with very low flexibility/stretchability. This study reports a solution processing method to prepare porous, amorphous, and elastic cellulose hydrogels and films. Native cellulose dissolved in a water-ZnCl2 mixture can form ionic gels through in situ polymerization of acrylic acid (AA) to poly(acrylic acid) (PAA). The addition of up to 30 vol % AA does not change the solubility of cellulose in the water-ZnCl2 mixture. After polymerization, the formation of interpenetrated networks, resulting from the chemical cross-linking of PAA and the ionic/coordination binding among cellulose/PAA and ZnCl2, gives rise to strong, transparent, and ionically conductive hydrogels. These hydrogels can be used for wearable sensors to detect mechanical deformation under stretching, compression, and bending. Upon removal of ZnCl2 and drying the gels, semitransparent amorphous cellulose composite films can be obtained with a Young's modulus of up to 4 GPa. The rehydration of these films leads to the formation of tough, highly elastic composites. With a water content of 3-10.5%, cellulose-containing films as strong as paper also show typical characteristics of elastomers with an elongation of up to 1300%. Such composite films provide an alternative solution to resolving the material sustainability of natural polymers without compromising their mechanical properties.

Application of fluorescent carbon quantum dots functional modified carboxymethyl cellulose film in toluene gas specific detection

With the increasing consumption of organic solvents in chemical and pharmaceutical industries, the environment pollution of volatile organic compounds (VOCs) has become an urgent problem. Therefore, the rapid-visual detection method is of great significance in the analysis of VOCs. Based on the fluorescence quenching/enhancement mechanism of carbon quantum dots (CQDs), with the help of carboxymethyl cellulose membrane with porous and large specific surface area structure, a series of green CQDs@carboxymethyl cellulose composite film (CQDs@CMC composite film) was prepared in this study. In the typical-targeted pollutants (toluene) detection application, a fluorescence spectroscopy method was established which could achieve the high sensitivity and strong specificity detection. The mainly conclusions were as follows: The fluorescence spectrometric detection method for toluene: A kind of hydrophobic Lmi/Bet CQDs@CMC composite film was prepared and characterized with imidazole/betaine CQDs and porous carboxymethyl cellulose composite film as raw materials. The toluene detection performance was studied, and the recognition mechanism was explored. The results showed that toluene enhanced the fluorescence of Lmi/Bet CQDs@CMC composite film. The fluorescence intensity of composite films was proportional to toluene concentration when the toluene concentration ranged from 200 to 2200 mg/L. The detection limit of toluene was 1.169 mg/L, which provides a theoretical basis for the detection of toluene by fluorescence spectrometry.

Preparation of the double cross-linking carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film for food active packaging application

This paper prepared a new kind of carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film with antibacterial properties. Carbon dots and citric acid were used as cross-linking agents, and polyvinyl alcohol and carboxymethyl cellulose were used as matrices respectively. The mechanical properties, UV shielding performance, thermal stability, antioxidant capability, and antibacterial activities of the carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film were researched. The prepared carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film was applied in the strawberry freshness preservation test. And test results indicated that the carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film could prevent rotting and extend the shelf life of strawberries. This carbon dots-polyvinyl alcohol-carboxymethyl cellulose composite film could be applied in the food active packaging field.

Preparation of benzothiocyanine‐carboxymethyl cellulose composite film and its antimicrobial properties

AbstractCellulose has a wide range of uses. It could be modified to create cellulose‐based hydrophobic materials and cellulose‐based conductive and stable flexible films, but it did not have antibacterial properties and was susceptible to bacterial erosion. In order to improve the utilization of cellulose materials and broaden the application of cellulose materials, cellulose could be given certain antibacterial properties by combining it with antimicrobial agents. This study focused on creating an organic antimicrobial agent, Benzothiocyanine (TCMTB), from CH2ClBr, and then developing a TCMTB‐CMC composite antimicrobial film by combining TCMTB with CMC. The successful synthesis of TCMTB was confirmed through NMR hydrogen spectroscopy testing. By varying the proportions of TCMTB in CMC, three types of composite antimicrobial cellulose film were produced. The study also assessed the impact of TCMTB on the mechanical strength of CMC film and tested the antimicrobial effectiveness of the composite film using the plate counting method. Results showed that the composite film had high inhibition rates, with 96.2% against Escherichia coli and 98.6% against Staphylococcus aureus. To establish a theoretical foundation for its use in seed encapsulation, leather preservation, and other applications.

Free-standing graphene oxide/carboxymethyl cellulose paper-based triboelectric nanogenerator for self-powered motion sensor

Triboelectric nanogenerators (TENG) are innovative energy-harnessing devices that serve as potential power sources for small portable electronics, operating on the principle of electrostatic induction. In this study, we demonstrate the fabrication of paper-like flexible graphene oxide/carboxymethyl cellulose (GO/CMC) composite film and their use as a tribo-positive layer in the TENG with fluorinated ethylene propylene (FEP) film as the tribo-negative layer. The GO/CMC TENG possesses high-energy harvesting performance compared to the bare CMC-based TENG that is due to the increase in surface charge of CMC due to the inclusion of GO sheets, as analyzed using Kelvin probe force microscopy (KPFM). The GO/CMC TENG device demonstrates an output voltage of 97 V and a short-circuit current of 1.2 µA, achieving a peak power of 41.4 µW, notably higher compared to state-of-the-art TENG devices. As a proof-of-concept, we also demonstrated the practical applicability of the GO/CMC TENG in day-to-day life for monitoring the human body motions and to drive portable electric devices, which ensures their candidature towards next-generation self-powered systems.

Antimicrobial topical polymeric films loaded with Acetyl-11-keto-β-boswellic acid (AKBA), boswellic acid and silver nanoparticles: Optimization, characterization, and biological activity

The study examined the antimicrobial and antioxidant potential of pure Acetyl-11-keto-β-boswellic acid (AKBA), boswellic acid (70%) and AKBA loaded nanoparticles as topical polymeric films. The optimized concentration (0.05 % w/v) of pure AKBA, boswellic acid (BA), and AKBA loaded silver nanoparticles were used to study its impact on film characteristics. Carboxymethyl cellulose (CMC), sodium alginate (SA), and gelatin (Ge) composite films were prepared in this study. The polymeric films were evaluated for their biological (antioxidant and antimicrobial activities) and mechanical characteristics such as tensile strength (TS) and elongation (%). Moreover, other parameters including water barrier properties and color attributes of the film were also evaluated. Furthermore, assessments were conducted using analytical techniques like FTIR, XRD, and SEM. Surface analysis revealed that AgNP precipitation led to a few particles in the film structure. Overall, the results indicate a relatively consistent microstructure. Moreover, due to the addition of AKBA, BA, and AgNPs, a significant decrease in TS, moisture content, water solubility, and water vapor permeation was observed. The films transparency also showed a decreasing trend, and the color analysis revealed decreasing yellowness (b*) of the films. Importantly, a significant increase in antioxidant activity against DPPH free radicals and ABTS cations was observed in the CSG films. Additionally, the AgNP-AKBA loaded films displayed significant antifungal activity against C. albicans. Moreover, the molecular docking analysis revealed the inter-molecular interactions between the AKBA, AgNPs, and composite films. The docking results indicate good binding of AKBA and silver nanoparticles with gelatin and carboxymethyl cellulosemolecules. In conclusion, these polymeric films have potential as novel materials with significant antioxidant and antifungal activities.

Cellulose-based separator woven by double-layer-configuration fibers for high S-load Li-S batteries

Lithium-sulfur (Li-S) battery with high theoretical energy density, has been the most promising next-generation energy storage devices. However, the capacity of the high S-loaded cathode decays rapidly due to the shuttling of soluble polysulfide intermediates between the two electrodes, which seriously inhibits its development. In this work, polyacrylonitrile (PAN) and cellulose composite film (PAN@CE) is designed, which is woven by double-layer configuration fiber. The outer layer of fiber is mainly composed of cellulose, and the inner layer is mainly PAN. From DFT calculations and experiments, the double-layer configuration enriched with nitrogen and oxygen groups can effectively inhibit the shuttle of soluble polysulfides. Meanwhile, the interlaced network structure of PAN@CE improves the electrolyte wettability and provides abundance transport paths for ions. In addition, the film also has good thermal stability. Hence, the cycling stability of Li-S batteries with PAN@CE as separator has been greatly improved. Cellulose-based Li-S battery with 9.1 mg S loading and an E/S ratio of 6.2 μL mg−1 is assembled. Its initial area capacity is 5.67 mAh cm−2. After 200 long cycles, the area capacity keeps above 4.0 mAh cm−2.

High-performance triboelectric-electromagnetic hybrid nanogenerator using dual-functional flexible neodymium iron boron/ethyl cellulose (NdFeB/EC) composite films for wind energy scavenging

Triboelectric-electromagnetic hybrid nanogenerator (HNG) with high output performance provides a very promising solution for realizing self-powered microelectronic devices. However, the complex structures and large mass of traditional HNGs make them difficult to prepare and carry. In this study, a rotating HNG based on flexible neodymium iron boron/ethyl cellulose (NdFeB/EC) composite films was designed for wind energy scavenging. A lightweight composite film with triboelectric and ferromagnetic properties, which can significantly reduce the weight of the rotor, was prepared to replace the magnet. Operated at a wind speed of 15.5 m/s, the triboelectric nanogenerator (TENG) unit of the optimized HNG with an interdigitated electrode gap of 2 mm can generate an open-circuit voltage (Voc) and a short-circuit current (Isc) of 55 V and 5.4 μA, respectively. The maximum power of TENG is 99.2 μW under the condition of an external load resistance of 10 MΩ. The corresponding electromagnetic generator (EMG) unit can produce Voc and Isc of approximately 0.16 V and 59.3 μA, delivering an output power of 2.5 μW at a matched loading resistance of 2.3 kΩ. Compared to the individual TENG or EMG units, the HNG exhibited better charging performance. A 470 μF capacitor can charge to 3.4 V within 600 s, and the stored energy can successfully power a commercial soil temperature–humidity meter to work continuously for 75 s and light 30 blue LEDs in parallel. This research is of great scientific significance for developing triboelectric–ferromagnetic dual-functional materials and designing highly integrated and lightweight HNGs.

The improvement of water barrier property in gelatin/carboxymethyl cellulose composite film by electrostatic interaction regulation and its application in strawberry preservation

Gelatin (GL) and carboxymethyl cellulose (CMC) are common natural components for edible films, but their water barrier performance are finite as hydrophilic polymers. In this study, a GL/CMC water barrier film was prepared, characterized and applied. The microstructure results showed that complex coacervation at pH 2.0 and cross-linking effect of sodium benzoate resulted in strong interaction forces and dense structure of this film. Compared with pure GL or CMC film, this novel composite film decreased water vapor permeability by approximately 90%, and possessed applicable water solubility (51.5%) and stronger barrier to oxygen and UV light. Acidic environment and sodium benzoate endowed antibacterial activity. Furthermore, the water barrier coating film decreased water loss by 47.8% and improved overall quality of fresh strawberries stored at 25 °C for 6 d. Therefore, the novel water barrier film based on complex coacervation and cross-linking is promising to control the postharvest quality of perishable berries.

Biodegradable, Strong, and Hydrophobic Regenerated Cellulose Films Enriched with Esterified Lignin Nanoparticles.

The scientific community is pursuing significant efforts worldwide to develop environmentally viable film materials from biomass, particularly transparent, high-performance regenerated cellulose (RC) films, to replace traditional plastics. However, the inferior mechanical performance and hydrophilic nature of RC films are generally not suitable for use as a substitute for plastics in practical applications. Herein, lignin homogenization is used to synthesize high-performance composite films. The esterified lignin nanoparticles (ELNPs) with dispersible and binding advantages are prepared through esterification and nanometrization. In the presence of ELNPs, RC films exhibit a higher tensile strength (110.4MPa), hydrophobic nature (103.6° water contact angle, 36.6% water absorption at 120min, and 1.127×10-12gcmcm-2s-1 Pa-1 water vapor permeability), and exciting optical properties (high visible and low ultraviolet transmittance). The films further display antioxidant activity, oxygen barrier ability, and thermostability. The films completely biodegrade at 12 and 30% soil moisture. Overall, this study offers new insights into lignin valorization and regenerated cellulose composite films as novel bioplastic materials.

Flexible regenerated cellulose composite films with sandwich structures for high-performance electromagnetic interference shielding

Flexible regenerated cellulose composite films with sandwich structures for high-performance electromagnetic interference shielding

Characterization of a Clove Essential Oil Slow-Release Microencapsulated Composite Film and Its Preservation Effects on Blueberry.

In order to extend the shelf life of fruits and vegetables, a sodium alginate-sodium carboxymethyl cellulose composite film loaded with poly(vinyl alcohol) microcapsules was prepared in this paper. The optimal film substrate ratios were obtained after the response surface optimization. Poly(vinyl alcohol) microcapsules were prepared, clove essential oil was loaded into them to investigate the effects of microcapsules on the composite film properties, and the microcapsule composite film with the best overall performance was selected to be applied to blueberry preservation. The results showed that the composite film of 0.84% sodium alginate, 0.25% sodium carboxymethyl cellulose, and 0.56% glycerol presented excellent mechanical properties after adding 1.75% microcapsules. It had a good inhibitory effect on Escherichia coli, Staphylococcus aureus, and Penicillium and had a DPPH clearance rate of 83.78%. The low-temperature bonded composite film could slow down the respiration rate of blueberry, inhibit browning and water loss, effectively maintain the quality of blueberry, and have a significant preservation effect on the anthocyanin and soluble solid content of blueberry. The clove essential oil slow-release microencapsulated composite film can be used for blueberry preservation.