A multifunctional biogenic films and coatings from synergistic aqueous dispersion of wood-derived suberin and cellulose nanofibers.

Here, biogenic and multifunctional active food coatings and packaging with UV shielding and antimicrobial properties were structured from the aqueous dispersion of an industrial byproduct, suberin, which was stabilized with amphiphilic cellulose nanofibers (CNF). The dual-functioning CNF, synthesized in a deep eutectic solvent, functioned as an efficient suberin dispersant and reinforcing agent in the packaging design. The nanofibrillar percolation network of CNF provided a steric hindrance against the coalescence of the suberin particles. The low CNF dosage of 0.5 wt% resulted in dispersion with optimal viscosity (208.70 Pa.s), enhanced stability (instability index of <0.001), and reduced particle size (9.37 ± 2.43 µm). The dispersion of suberin and CNF was further converted into self-standing films with superior UV-blocking capability, good thermal stability, improved hydrophobicity (increase in water contact angle from 61° ± 0.15 to 83° ± 5.11), and antimicrobial properties against gram-negative bacteria. Finally, the synergistic bicomponent dispersions were demonstrated as fruit coatings for bananas and packaging for strawberries to promote their self-life. The coatings and packaging considerably mitigated fruit deterioration and improved their freshness by preventing moisture loss and microbial attack. This sustainable approach is expected to pave the way toward advanced, biogenic, and active food packaging based on widely available bioresources.

Pickering Emulsions and Hydrophobized Films of Amphiphilic Cellulose Nanofibers Synthesized in Deep Eutectic Solvent.

Herein, a dual-functioning deep eutectic solvent system based on triethylmethylammonium chloride and imidazole was harnessed as a swelling agent and a reaction medium for the esterification of cellulose with n-octyl succinic anhydride (OSA). The modified or amphiphilic cellulose nanofibers (ACNFs), synthesized using three different OSA-to-anhydroglucose unit molar ratios (0.5:1, ACNF-1; 1:1, ACNF-2; and 1.5:1, ACNF-3), were further converted into nanofibers with degree of substitution (DS) values of 0.24-0.66. The ACNFs possessed a lateral dimension of 4.24-9.22 nm and displayed surface activity due to the balance of hydrophobic and hydrophilic characteristics. The ACNFs made stable aqueous dispersions; however, the instability index of ACNF-3 (0.51) was higher than those of ACNF-1 (0.29) and ACNF-2 (0.33), which was attributed to the high DS-induced hydrophobicity, causing the instability in water. The amphiphilic nature of ACNFs promoted their performance as stabilizers in oil-in-water Pickering emulsions with average droplet sizes of 4.85 µm (ACNF-1) and 5.48 µm (ACNF-2). Self-standing films of ACNFs showed high contact angles for all the tested DS variants (97.48-114.12°), while their tensile strength was inversely related to DS values (ACNF-1: 115 MPa and ACNF-3: 49.5 MPa). Aqueous dispersions of ACNFs were also tested for coating fruits to increase their shelf life. Coatings improved their shelf life by decreasing oxygen contact and moisture loss.

Highly effective fractionation chemistry to overcome the recalcitrance of softwood lignocellulose.

The efficient fractionation and thus production of individual biomass components are pivotal processes in the biorefinery concept. However, the recalcitrant nature of lignocellulose biomass, especially in the case of softwood, is one of the main obstacles to the wider application of biomass-based chemicals and materials. In this study, the use of aqueous acidic systems in the presence of thiourea was studied for the fractionation of softwood in mild conditions. Despite relatively low temperature (100 °C) and treatment times (30-90 min), notable high lignin removal efficiency (approximately 90 %) was obtained. Chemical characterization and the isolation of minor fraction of cationic, water-soluble lignin indicated that the fractionation proceed via nucleophilic addition of thiourea to lignin, resulting in dissolution of lignin in acidic water in relatively mild conditions. Besides high fractionation efficiency, both fiber and lignin fractions were obtained with bright color, significantly elevating their usability in material applications.

High Oxygen Barrier Polyester from 3,3'-Bifuran-5,5'-dicarboxylic Acid.

An exceptional oxygen barrier polyester prepared from a new biomass-derived monomer, 3,3'-bifuran-5,5'-dicarboxylic acid, is reported. When exposed to air, the furan-based polyester cross-links and gains O2 permeability 2 orders of magnitude lower than initially, resulting in performance comparable to the best polymers in this class, such as ethylene-vinyl alcohol copolymers. The cross-links hinder the crystallization of amorphous samples, also rendering them insoluble. The process was observable via UV-vis measurements, which showed a gradual increase of absorbance between wavelengths of 320 and 520 nm in free-standing films. The structural trigger bringing about these changes appears subtle: the polyester containing 5,5'-disubstituted 3,3'-bifuran moieties cross-linked, whereas the polyester with 5,5'-disubstituted 2,2'-bifuran moieties was inert. The 3,3'-bifuran-based polyester is effectively a semicrystalline thermoplastic, which is slowly converted into a cross-linked material with intriguing material properties once sufficiently exposed to ambient air.

Insights into the role of molar ratio and added water in the properties of choline chloride and urea-based eutectic mixtures and their cellulose swelling capacity.

Eutectic mixtures and deep eutectic solvents (DESs) are promising green media for the pre-treatment of lignocellulose materials. They can be harnessed for the swelling of cellulose and further facilitate cellulose hydrolysis, derivatization, and production of cellulose-based (nano) materials. Several studies indicated that water can take part in the formation of the nanostructure of DES; however, it is still unclear how additional water influences many important properties and functioning of DES, especially when the molar ratio of compounds differs from the eutectic point composition. Here, viscosity, pH, conductivity, solvatochromic and solvatomagnetic solvent parameters, and fiber swelling capacity of choline chloride and urea mixtures demonstrating different molar ratios were investigated in the presence and absence of added water. The participation of water in the formation of molecular clusters with choline chloride and urea was indicated by viscosity, pH, and conductivity measurements. Hydrogen bond acceptor values of aqueous mixtures increased as a function of water content, and the results obtained using both methods were in line, indicating their suitability for the determination of hydrogen bond acidity of aqueous choline chloride-urea mixtures. However, hydrogen bond basicity determined by solvatochromic and magnetic methods exhibited almost opposite trends. The close investigation of the chemical shift of solvatomagnetic probes indicated that the chemical environment of the choline chloride-urea (1 : 2) mixture remained constant until the water content of 30 wt% was in line with previous molecular simulations. When cellulose fibers were treated with mixtures under mixing, the non-ideality of the choline chloride-urea mixture and the absence of water were found to be advantageous; however, aqueous mixtures efficiently increased the diameters of cellulose fibers in the absence of mixing, and water-containing mixtures appeared to be appealing systems for cellulose pretreatments.

Renewable Furfural-Based Polyesters Bearing Sulfur-Bridged Difuran Moieties with High Oxygen Barrier Properties.

With the goal of achieving high barrier with bio-based materials, for example, for packaging applications, a series of novel furfural-based polyesters bearing sulfide-bridged difuran dicarboxylic acid units with high oxygen barrier properties were synthesized and characterized. For the novel poly(alkylene sulfanediyldifuranoate)s, a 11.2-1.9× higher barrier improvement factor compared to amorphous poly(ethylene terephthalate) was observed which places the novel polyesters in the top class among previously reported 2,5-furandicarboxylic acid (FDCA) and 2,2'-bifuran-based polyesters. Titanium-catalyzed polycondensation reactions between the novel synthesized monomer, dimethyl 5,5'-sulfanediyldi(furan-2-carboxylate), and four different diols, ethylene glycol, 1,3-propanediol, 1,4-butanediol, and 1,5-pentanediol, afforded difuran polyesters with high intrinsic viscosities (0.76-0.90 dL/g). These polyesters had good thermal stability, decomposing at 342-363 and 328-570 °C under nitrogen and air, respectively, which allowed processing them into free-standing films via melt-pressing. In tensile testing of the film specimens, tensile moduli in the range of 0.4-2.6 GPa were recorded, with higher values observed for the polyesters with shorter diol units. Interestingly, besides the low oxygen permeability, the renewable sulfide-bridged furan monomer also endowed the polyesters with slight UV shielding effect, with cutoff wavelengths of ca. 350 nm, in contrast to FDCA-based polyesters, which lack significant UV light absorption at over 300 nm.

Fast and Filtration-Free Method to Prepare Lactic Acid-Modified Cellulose Nanopaper.

Dewatering in the preparation of cellulose nanopapers can take up to a few hours, which is a notable bottleneck in the commercialization of nanopapers. As a solution, we report a filtration-free method that is capable of preparing lactic acid-modified cellulose nanopapers within a few minutes. The bleached cellulose nanofibers (CNFs), obtained using a Masuko grinder, were functionalized by sonication-assisted lactic acid modification and centrifuged at 14 000 rpm to achieve a doughlike, concentrated mass. The concentrated CNFs were rolled into a wet sheet and dried in a vacuum drier to obtain nanopapers. The nanopaper preparation time was 10 min, which is significantly faster than the earlier time period reported in the literature (up to a few hours of preparation time). The mechanical properties of nanopaper were comparable to the previous values reported for nanopapers. In addition, the method was successfully used to prepare highly conductive functional nanopapers containing carboxylated multiwalled carbon nanotubes.

A Fast Dissolution Pretreatment to Produce Strong Regenerated Cellulose Nanofibers via Mechanical Disintegration.

This study investigates a fast dissolution and regeneration pretreatment to produce regenerated cellulose nanofibers (RCNFs) via mechanical disintegration. Two cellulose pulps, namely, birch and dissolving pulps, with degree of polymerizations of 1800 and 3600, respectively, were rapidly dissolved in dimethyl sulfoxide (DMSO) by using tetraethylammonium hydroxide (TEAOH) as aqueous electrolyte at room temperature. When TEAOH (35 wt % in water) was added to the pulp-DMSO dispersion (pulp:DMSO and TEAOH:DMSO weight ratios of 1:90 and 1:9, respectively), 95% of the dissolving pulp and 85% of the birch pulp fibers dissolved almost immediately. Addition of water caused the regeneration of cellulose without any chemical modification and only a minor decrease of DP, whereas the crystallinity structure of cellulose transformed from cellulose I to cellulose II. The regenerated cellulose could then be mechanically disintegrated into nanosized fibers with only a few passes through a microfluidizer, and RCNF showed fibrous structure. The specific tensile strength of the film produced from both RCNFs exceeded 100 kN·m/kg, and overall mechanical properties of RCNF produced from birch pulp were in line with reference CNF produced by using extensive mechanical disintegration. Although the thermal stability of RCNFs was slightly lower compared to their corresponding original cellulose pulp, the onset temperature of degradation of RCNFs was over 270 °C.

Aqueous Modification of Chitosan with Itaconic Acid to Produce Strong Oxygen Barrier Film.

In this study, the chemical modification of chitosan using itaconic acid as a natural-based unsaturated dicarboxylic acid was investigated. In an aqueous environment, the amine group of chitosan reacts with itaconic acid to produce a chitosan derivative with pyrrolidone-4-carboxylic acid group. On the basis of the elemental analysis, 15% of the amine groups of chitosan reacted, thus creating modified chitosan with amine and carboxylic acid functionalities. Due to the presence of amine and carboxylic acid groups, the surface charge properties of the chitosan were notably altered after itaconic acid modification. In an aqueous solution, the modified chitosan exhibited zwitterionic properties, being cationic at low pH and turning anionic when the pH was increased over 6.5, whereas the original chitosan remained cationic until pH 9. Furthermore, it was demostrated that the modified chitosan was suitable for the preparation of a self-standing film with similarly high transparency but notably higher mechanical strength and oxygen barrier properties compared to a film made from the original chitosan. In addition, the thermal stability of the modified chitosan film was higher than that of the original chitosan film, and the modified chitosan exhibited flame-retardant properties.

Review: Periodate oxidation of wood polysaccharides-Modulation of hierarchies.

Periodate oxidation of polysaccharides has transitioned from structural analysis into a modification method for engineered materials. This review summarizes the research on this topic. Fibers, fibrils, crystals, and molecules originating from forests that have been subjected to periodate oxidation can be crosslinked with other entities via the generated aldehyde functionality, that can also be oxidized or reduced to carboxyl or alcohol functionality or used as a starting point for further modification. Periodate-oxidized materials can be subjected to thermal transitions that differ from the native cellulose. Oxidation of polysaccharides originating from forests often features oxidation of structures rather than liberated molecules. This leads to changes in macro, micro, and supramolecular assemblies and consequently to alterations in physical properties. This review focuses on these aspects of the modulation of structural hierarchies due to periodate oxidation.

Surface Modification of Cured Inorganic Foams with Cationic Cellulose Nanocrystals and Their Use as Reactive Filter Media for Anionic Dye Removal.

In this work, a surface cationized inorganic-organic hybrid foam was produced from porous geopolymer (GP) and cellulose nanocrystals (CNCs). GPs were synthesized from alkali-activated metakaolin using H2O2 as a blowing agent and hexadecyltrimethylammonium bromide (CTAB) as a surfactant. These highly porous GPs were combined at pH 7.5 with cationic CNCs that had been synthesized from dissolving pulp through periodate oxidation followed by cationization in a deep eutectic solvent. The GP-CNC hybrid foams were employed as reactive filters in the removal of the anionic dye, methyl orange (MO; 5-10 mg/L, pH 7). The effects of a mild acid wash and thermal treatments on the structure, properties, and adsorption capacity of the GPs with CNCs and MO were investigated. The CNCs aligned as films and filaments on the surfaces of the neutralized GPs and the addition of CNCs improved MO removal by up to 84% compared with the reference sample. In addition, CTAB was found to disrupt the attachment of CNCs on the pores and improve adsorption of MO in the GPs with and without CNCs.

Lignin-rich sulfated wood nanofibers as high-performing adsorbents for the removal of lead and copper from water.

Lignin-rich wood nanofibers (WNFs) were investigated as adsorbents for heavy metals. Lignin-free cellulose nanofibers (CNFs) produced from bleached cellulose fibers were used as a reference. Two raw materials were used to produce WNFs: groundwood pulp as industrially produced wood fibers and sawdust as an abundantly available low-value industrial side stream. WNFs and reference CNFs were produced using a reactive deep eutectic solvent to obtain nanofibers with abundant sulfate groups on their surfaces. With a similar amount of sulfate groups, WNFs had a higher adsorbent performance compared to CNFs and, at low metal concentrations (0.24 mmol/l), the removal of both metals was almost quantitate with WNFs. However, it was noted that, at pHs 4 and 5, the sodium present in the buffer solution interfered with the adsorption, leading to lower adsorption capacities compared to the capacity at pH 3. In addition, in the case of lead, the adsorption capacity dramatically decreased at a high metal concertation, indicating that a high lead concentration results in the saturation of adsorption sites of sulfated nanofibers, leading to a decreased adsorption capacity. Nevertheless, it was observed that WNFs had a higher tolerance to high metal concentrations than CNFs.

Carbamation of Starch with Amine Using Dimethyl Carbonate as Coupling Agent.

A one-pot coupling of starch with alkyl amine was studied using dimethyl carbonate (DMC) as the coupling agent. Although reaction occurred without a catalyst (24 h, 70 °C), different catalysts, namely, imidazole, tetramethylguanidine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and combinations thereof were investigated to improve the reaction efficiency. When 20 mol % DBU was used as a catalyst, the degree of substitution (DS) could be improved from 0.05 to 0.15 compared to the noncatalyzed reaction. When the amount of DBU was decreased to 5 mol %, catalytical activity remained, albeit with a slightly lower DS (0.09). Temperature did not have a significant effect on the DS but it could be used to alter the solubility of the product. Based on chemical analysis, the alkyl group was attached to starch by the formation of a carbamate group. As the carbonyl carbon in the carbamate originated from DMC, which, in turn, can be produced from carbon dioxide on an industrial scale, the current study provides a conventional way to utilize carbon dioxide-based chemicals in the functionalization of a natural polymer. DMC is also biodegradable and classified as a nonvolatile organic component, making it an environmentally desirable coupling agent.

Hybrid films of cellulose nanofibrils, chitosan and nanosilica-Structural, thermal, optical, and mechanical properties.

Organic-inorganic hybrid films were fabricated from cellulose nanofibrils (CNF) and nanosilica (5-30% wt) embedded in a chitosan (Chi) biopolymer matrix using a slow evaporation method. The self-standing films exhibited high strength and modulus up to 120 ± 5 MPa and 7.5 ± 0.4 GPa, respectively, which are remarkably high values for biopolymer/chitosan hybrids. Scanning electron microscopy showed that the nanosilica is formed of larger aggregates within the lamellar CNF network structure. This observation was further confirmed using synchrotron-based scanning transmission x-ray microscopy (STXM) with the capability to determine the spatial and chemical distribution analysis of the constituents of films. It is interesting that the thermal stability of the hybrid films improved as the nanosilica content increased. Furthermore, the nanosilica effectively filled the pores in the CNF network, thus decreasing the UV transmission and the visible light transmittance of the films.

Highly Transparent Nanocomposites Based on Poly(vinyl alcohol) and Sulfated UV-Absorbing Wood Nanofibers.

Unbleached lignocellulose fibers were studied for the fabrication of wood-based UV-absorbing nanofibers and were used to produce transparent nanocomposites. Groundwood pulp (GWP) and sawdust were selected as raw materials thanks to their low processing degree of fibers and abundant availability as a low-value industrial side stream. Both materials were first sulfated using a reactive deep eutectic solvent. The sulfated wood and sawdust nanofibers (SWNFs and SSDNFs, respectively) were fabricated using a mild mechanical disintegration approach. As a reference material, sulfated cellulose nanofibers (SCNFs) were obtained from bleached cellulose pulp. Our results showed that both GWP and sawdust exhibited similar reactivity compared with bleached cellulose pulp, whereas the yields of sulfated lignin-containing pulps were notably higher. The diameters of both SWNFs and SSDNFs were approximately 3 nm, which was similar to those of the SCNFs. When 10 wt % of lignin-containing nanofibers were mixed together with poly(vinyl alcohol), the fabrication of nanocomposites with only a minimal decrease in transparency in the visible light spectrum was achieved. Transmission in the UV region, on the other hand, was significantly reduced by SWNFs and SSDNFs, whereas SCNFs had only a minor UV-absorbing property. Although the reinforcing effect of lignin-containing nanofibers was lower compared with that of SCNFs, it was comparable with those of other UV-absorbing additives reported in the literature. Overall, the wood-based UV-absorbing nanofibers could have a valuable use in optical applications such as lenses and optoelectronics.

A fast method to prepare mechanically strong and water resistant lignocellulosic nanopapers.

This study covers a green method to prepare hybrid lignocellulosic nanopapers by combining wood nanofibres (WNFs) and cellulose nanofibres (CNFs). The WNFs and CNFs behave synergistically to compensate for the drawbacks of each other resulting in enhanced hybrid nanopapers. The draining time of hybrid nanopapers was improved by up to 75% over CNF nanopaper, and the mechanical properties, modulus, strength and elongation, were respectively improved up to 35%, 90% and 180% over WNF nanopaper. Additionally, the water resistance of hybrid nanopapers was considerably improved with a water contact angle of 95°; the neat CNF nanopaper had a contact angle of 52°. The morphology of nanopapers, studied by electron microscopy, indicated that lignin acts as a matrix, which binds the nanofibres together and makes them impervious to external environmental factors, such as high humidity. The reported hybrid nanopapers are 100% bio-based, prepared by a simple and environmentally friendly processing route. Reported hybrid nanopapers can be used in novel applications such as gas barrier membranes and printable electronics.

Emulsion Stabilization with Functionalized Cellulose Nanoparticles Fabricated Using Deep Eutectic Solvents.

In this experiment, the influence of the morphology and surface characteristics of cellulosic nanoparticles (i.e., cellulose nanocrystals [CNCs] and cellulose nanofibers [CNFs]) on oil-in-water (o/w) emulsion stabilization was studied using non-modified or functionalized nanoparticles obtained following deep eutectic solvent (DES) pre-treatments. The effect of the oil-to-water ratio (5, 10, and 20 wt.-% (weight percent) of oil), the type of nanoparticle, and the concentration of the particles (0.05⁻0.2 wt.-%) on the oil-droplet size (using laser diffractometry), o/w emulsion stability (via analytical centrifugation), and stabilization mechanisms (using field emission scanning electron microscopy with the model compound-i.e., polymerized styrene in water emulsions) were examined. All the cellulosic nanoparticles studied decreased the oil droplet size in emulsion (sizes varied from 22.5 µm to 8.9 µm, depending on the nanoparticle used). Efficient o/w emulsion stabilization against coalescence and an oil droplet-stabilizing web-like structure were obtained only, however, with surface-functionalized CNFs, which had a moderate hydrophilicity level. CNFs without surface functionalization did not prevent either the coalescence or the creaming of emulsions, probably due to the natural hydrophobicity of the nanoparticles and their instability in water. Moderately hydrophilic CNCs, on the other hand, distributed evenly and displayed good interaction with both dispersion phases. The rigid structure of CNCs meant, however, that voluminous web structures were not formed on the surface of oil droplets; they formed in flat, uniform layers instead. Consequently, emulsion stability was lower with CNCs, when compared with surface-functionalized CNFs. Tunable cellulose nanoparticles can be used in several applications such as in enhanced marine oil response.

Cationization of lignocellulosic fibers with betaine in deep eutectic solvent: Facile route to charge stabilized cellulose and wood nanofibers.

In this study, a deep eutectic solvent (DES [based on triethylmethylammonium chloride (TEMA) and imidazole]) was used as a reaction medium for cationization of cellulose fibers with trimethylglycine (betaine) hydrochloride in the presence of p-Toluenesulfonyl (tosyl) chloride. Cellulose betaine ester with a cationic charge up to 1.95 mmol/g was obtained at mild reaction conditions (four hours at 80 °C). The reaction was further demonstrated in the fabrication of cationic cellulose nanofibers (CCNFs) by a mild mechanical disintegration of cationized cellulose. In addition to CCNFs, cationic wood nanofibers (CWNFs) were produced directly from groundwood pulp (GWP) with a high lignin content (27 w%). Individualized CCNFs and CWNFs had a fiber diameter of 4.7 ±â€¯2.0 and 3.6 ±â€¯1.3 nm, respectively, whereas some larger fiber aggregates (diameter below 200 nm) were also observed, especially in the case of CWNFs.

Recyclable deep eutectic solvent for the production of cationic nanocelluloses.

Deep eutectic solvents (DESs) are potential green systems that can be used as reagents, extraction agents and reaction media. DESs are often biodegradable, easy to prepare and have low toxicity. In this work, a recyclable DES formed from aminoguanidine hydrochloride and glycerol (AhG) was used as a reaction medium and reagent (aminoguanidine hydrochloride) for the production of cationic nanocelluloses. Under mild conditions (i.e., a reaction time of 10 min at 70 °C), dialdehyde celluloses (DACs) with two different aldehyde contents (2.18 and 3.79 mmol g-1) were cationized by AhG DES to form cationic dialdehyde celluloses (CDACs). Both CDACs achieved a similar high charge density of approximately 1.1 mmol g-1. At 80 °C (for 10 min), a very high cationic charge density of 2.48 mmol g-1 was obtained. The recyclability of AhG DES was demonstrated by reusing it five times without decreasing the reaction efficiency. In particular, due to the low consumption of amoniguanidine hydrochloride, high recycling efficiency could be achieved without the use of any additional chemicals. The cationized celluloses, CDACs, were further mechanically disintegrated to obtain cationic nanocelluloses. According to the initial aldehyde content of DACs, the morphology of the nanocellulose could be tailored to produce highly cationic cellulose nanofibrils (CNFs) or cellulose nanocrystals (CNCs). Transmission electron microscopy confirmed that individual CNFs and CNCs with an average width of 4.6 ±â€¯1.1 nm and 5.7 ±â€¯1.3 nm, respectively, were obtained. Thus, the results presented here indicate that the AhG DES is a promising green and recyclable way of producing cationized CNFs and CNCs.

Stereoselectively water resistant hybrid nanopapers prepared by cellulose nanofibers and water-based polyurethane.

Cellulose nanopapers, known for excellent mechanical properties, loses 90% of their stiffness in the wet conditions. In this study, we attempt to improve the wet mechanical properties of cellulose nanopaper by incorporating polyurethane by a novel and ecofriendly method. Water based PU was dispersed along with CNFs in water and hybrid nanopapers were prepared by draining water under vacuum followed by forced drying. These hybrid nanopapers have a gradient interpenetrating structure with PU concentrated towards one side and CNFs towards the other, which was confirmed by scanning electron microscopy, x-ray photoelectron spectroscopy and contact angle measurements. Because of this, the nanopapers are water resistant on one surface (PU rich side) and hydrophilic on the other (cellulose rich side), making them stereoselectively water resistant. When wetted with water on the PU side, the hybrid nanopaper with 10% PU is able to retain 65% modulus; on the other hand, the reference retains only 10% of the modulus. Similar results are seen in the tensile and the yield strength. Additionally, the hybrid nanopapers have higher elongation and improved thermal stability. The reported material is relevant to the applications such as flexible electronics and transparent displays.