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Cellulose nanocrystals (CNCs) and chitosan (Cht) have been studied extensively for oxygen and water vapour barrier coatings in biodegradable, compostable or recyclable paper packaging. However, rare studies have been performed by using scalable, inexpensive, and fast continuous slot-die coating processes, and none yet in combination with fast' and high-throughput near-infrared (NIR) light energy drying. In this frame, we studied the feasibility of a moderately concentrated (11 wt%) anionic CNC and (2 wt%) cationic Cht coating (both containing 20 wt% sorbitol related to the weight of CNC/Cht), by using plain and pigment pre-treated papers. The effect of coating parameters (injection speed, dry thickness settings) were investigated on coating quantity (dry weight, thickness) and homogeneity (coverage), papers' structure (thickness, grammage, density), whiteness, surface wettability, barrier (air, oxygen and water vapour) properties and adhesion (surface strength). The coating homogeneity was dependent primarily on the suspensions' viscosity, and secondarily on the applied coating parameters, whereby CNCs could be applied at 1–2 times higher injection speeds (up to 80 mL/min) and versatile coating weights, but required a relatively longer time to dry. The CNCs thus exhibited outstanding air (4.2–1.5 nm/Pa s) and oxygen (2.7–1.1 cm3 mm/m2 d kPa) barrier performance at 50% RH and 22–33 g/m2 deposition, whereas on top deposited Cht (3–4 g/m2) reduced its wetting time and improved the water vapour barrier (0.23–0.28 g mm/m2 d Pa). The balanced barrier properties were achieved due to the polar characteristic of CNCs, the hydrophobic nature of Cht and the quantity of the applied bilayer coating that can provide sustainable paper-based packaging. [ABSTRACT FROM AUTHOR]

Purpose: The purpose of this study is to find an applicable solution for the consolidation of petrified paper after disassembling it to complete other stages of treatment. Design/methodology/approach: The samples were subjected to natural aging by being inoculated with Aspergillus niger until they reached the stage of adhesion and petrification. After that, the leaves were separated, and cellulose nanocrystals were applied, then the leaves were subjected to wet thermal aging for 21 days. Digital microscope, scanning electron microscope, mechanical properties measurement, measurement of color change, Fourier transform infrared spectroscopy and pH measurement were used to evaluate the effects of the cellulose nanocrystal on paper. Findings: The results proved that cellulose nanocrystal (5%) successes consolidation of petrified paper Without affecting its natural, mechanical and chemical properties. Originality/value: This study was based on the effectiveness of cellulose nanocrystal in strengthening the petrified papers and testing its effect on the physical, mechanical and chemical paper properties. [ABSTRACT FROM AUTHOR]

Green nanocomposites combining cellulose nanofibrils (CNFs), cellulose nanocrystals (CNCs), and lignin nanoparticles (LNPs) were designed and applied for the first time as ternary protective coatings on cellulosic materials, i.e., substrates mainly composed of cellulose. All the nanostructures were obtained from elephant grass biomass. CNFs and CNCs are less than 10 nm thick and present a filament-like morphology, while LNPs are spheres with an average diameter of less than 100 nm. The use of water-based nanoparticle dispersions is a facile and greener alternative to synthetic varnishes usually based on toxic organic solvents. Moreover, the coatings from renewable sources were chemically stable; showed high compatibility with wood, paper, and fabric; and preserved the roughness and surface morphology of the substrates after application. Moist-heat accelerated aging and UV-shielding assays revealed that the nanocellulose/nanolignin coatings were able to protect the coated cellulosic substrates against degradation. The wettability of nanocomposite-coated substrates could be tailored and reduced to produce hydrophobic surfaces by applying additional layers of water-based carnauba wax nanoparticles, which are also sustainable. Additionally, two-dimensional infrared spectroscopy mapping confirmed the reversibility of the coating application, as the nanocomposite layers could be easily removed from the cellulosic substrates by water-loaded cleaning hydrogels. Therefore, the functional protective coating introduced here represents an environmentally friendly and nontoxic approach for the conservation of cellulosic artifacts in general, including cultural heritage objects based on paper, wood, and fabric. [ABSTRACT FROM AUTHOR]

Nanocellulose has received enormous scientific interest for its abundance, easy manufacturing, biodegradability, and low cost. Cellulose nanocrystals (CNCs) and cellulose nanofibers (CNFs) are ideal candidates to replace plastic coating in the textile and paper industry. Thanks to their capacity to form an interconnected network kept together by hydrogen bonds, nanocelluloses perform an unprecedented strengthening action towards cellulose‐ and other fiber‐based materials. Furthermore, nanocellulose use implies greener application procedures, such as deposition from water. The surface chemistry of nanocellulose plays a pivotal role in influencing the performance of the coating: tailored surface functionalization can introduce several properties, such as gas or grease barrier, hydrophobicity, antibacterial and anti‐UV behavior. This review summarizes recent achievements in the use of nanocellulose for paper and textile coating, evidencing critical aspects of coating performances related to deposition technique, nanocellulose morphology, and surface functionalization. Furthermore, beyond focusing on the aspects strictly related to large‐scale coating applications for paper and textile industries, this review includes recent achievements in the use of nanocellulose coating for the safeguarding of Cultural Heritage, an extremely noble and interesting emerging application of nanocellulose, focusing on consolidation of historical paper and archaeological textile. Finally, nanocellulose use in electronic devices as an electrode modifier is highlighted. [ABSTRACT FROM AUTHOR]

Strongly degraded cellulosic artworks usually need deacidification and consolidation. Alkaline nanoparticles are known to be effective in neutralizing the acidity, while cellulose nanocrystals have the potential to be used as compatible and effective strengthening agents. We have grafted cellulose nanocrystals with oleic acid using a 1′1-carbonyldiimidazole-mediated procedure, to increase their dispersibility in organic solvents, and synthesized Ca(OH) 2 or CaCO 3 nanoparticles via a solvothermal process. Grafted nanocellulose and alkaline nanoparticles were used to prepare ethanol-based "hybrids". Prior to the application, the physico-chemical properties of nanocellulose dispersions and "hybrids" were studied by rheology and small-angle X-ray scattering. Cellulose nanocrystals were effectively grafted and stably dispersed in ethanol. It was shown that the use of ethanol as a dispersing medium, and the addition of alkaline nanoparticles act in a synergistic way, increasing the interactions between grafted cellulose nanocrystals, leading to the formation of clusters. These dispersions are thixotropic, a behavior particularly appealing to conservation purposes, since they can be applied in the liquid state, or, when a more confined application is required, they can be applied in a gel-like state. As a result of the application, an improvement in the mechanical properties of paper and an increase of pH were obtained. [ABSTRACT FROM AUTHOR]

Paper waste is a raw material for a lot of products with different added value. The engineering, economic and environmental aspects of paper waste recycling are analysed for production of composite material, cellulose nanofibers and nanocrystals, bricks with paper components, porous carbon, film of biopolymer, enzymatic sugar and bioenergy: bioethanol, hydrogen and biofuel. Through multicriteria analysis, it was possible to determine the most feasible paper waste recycling product in case of four product groups: egg packaging boxes, cardboard, reused paper, cellulose nanomaterials (nanofibers and nanocrystals). The production of cellulose nanofibres and cellulose nanocrystals has an advantage over egg packaging and cardboard production as well as reusable paper. [ABSTRACT FROM AUTHOR]

Currently, there is an increasing interest in the use of biopolymers in industrial applications to replace petroleum-based additives, since they are abundantly available, renewable and sustainable. Cottonseed protein is a biopolymer that, when used as a modifier, has shown improved performance for wood adhesives and paper products. Thus, it would be useful to explore the feasibility of using cellulose nanomaterials to further improve the performance of cottonseed protein as a paper strength agent. This research characterized the performance of cottonseed protein isolate with/without cellulose nanofibers (CNFs) and cellulose nanocrystals (CNCs) to increase the dry strength of filter paper. An application of 10% protein solution with CNCs (10:1) or CNFs (50:1) improved the elongation at break, tensile strength and modulus of treated paper products compared to the improved performance of cottonseed protein alone. Further analysis using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) indicated that the cottonseed protein/nanocellulose composites interacted with the filter paper fibers, imparting an increased dry strength.

In this review, we summarize the recent progress in thermal conductivity analysis of nanocellulose materials called cellulose nanopapers, and compare them with polymeric materials, including neat polymers, composites, and traditional paper. It is important to individually measure the in-plane and through-plane heat-conducting properties of two-dimensional planar materials, so steady-state and non-equilibrium methods, in particular the laser spot periodic heating radiation thermometry method, are reviewed. The structural dependency of cellulose nanopaper on thermal conduction is described in terms of the crystallite size effect, fibre orientation, and interfacial thermal resistance between fibres and small pores. The novel applications of cellulose as thermally conductive transparent materials and thermal-guiding materials are also discussed. [ABSTRACT FROM AUTHOR]

Well-dispersed Fe 3 O 4 nanoparticles (NPs) were synthesized by a co-precipitation method in the presence of cellulose nano-crystals (CNC) as the template. The thus prepared Fe 3 O 4 NPs were then used as a coating agent for the preparation of conductive paper. Fourier transform infrared spectroscopy (FTIR) results revealed that the Fe 3 O 4 NPs were immobilized on the CNC through interactions between the hydroxyl groups of CNC and Fe 3 O 4 . Scanning transmission electron microscopy (STEM) images showed that the Fe 3 O 4 NPs prepared in the presence of CNC can be dispersed in the CNC network, while the Fe 3 O 4 NPs prepared in the absence of CNC tended to aggregate in aqueous solutions. The conductivity of the Fe 3 O 4 NPs coated paper can reach to 0.0269 S/m at the coating amount of 14.75 g/m 2 Fe 3 O 4 /CNC nanocomposites. Therefore, the thus obtained coated paper can be potentially used as anti-static packaging material in the packaging field. [ABSTRACT FROM AUTHOR]

Cellulose nanofibers have been showing much greater potential to enhance the mechanical and physical properties of polymer-based composite materials. The purpose of this study is to extract the cellulose nanofibers from waste bio-resources; such as waste newspaper and paper sludge. The cellulosic raw materials were treated chemically and physically in order to extract individualized cellulose nanofiber. The combination of acid hydrolysis and following mechanical treatment resulted in the extraction of cellulose nanofibers having diameter of about 40 nm. In order to examine the reinforcing effect of the extracted cellulose nanofibers, fully biodegradable green nanocomposites were fabricated by composing polyvinyl alcohol (PVA) resin with the extracted cellulose nanofibers, and then the tensile tests were conducted. The results showed that the enhancement in mechanical properties was successfully obtained in the cellulose nanofiber/PVA green nanocomposites. [ABSTRACT FROM AUTHOR]

Alkenyl succinic anhydride (ASA) is a reactive sizing agent that can impart good water repellence to paper by decreasing the wettability of the cellulose fibers. However, ASA can undergo hydrolysis, which is detrimental to the ASA sizing efficiency. In order to improve the ASA emulsion stability and ASA sizing efficiency, we used cationically modified cellulose nanocrystals (CNCs) to stabilize the cationic starch-emulsified ASA. Transmission electron microscope observation revealed that ASA droplets were well shielded by both the cationic CNCs and cationic starch, which may be responsible for the improved stabilization of ASA. The Hercules size test sizing degree, contact angle and particle size measurements demonstrated that cationic CNCs-ASA sized paper exhibited improved results in comparison with the control (without cationic CNCs under otherwise the same conditions). Furthermore, the resulting cationic CNCs-ASA system can improve the tensile index and burst index of the sized paper. [ABSTRACT FROM AUTHOR]

Currently, there is an increasing interest in the use of biopolymers in industrial applications to replace petroleum-based additives, since they are abundantly available, renewable and sustainable. Cottonseed protein is a biopolymer that, when used as a modifier, has shown improved performance for wood adhesives and paper products. Thus, it would be useful to explore the feasibility of using cellulose nanomaterials to further improve the performance of cottonseed protein as a paper strength agent. This research characterized the performance of cottonseed protein isolate with/without cellulose nanofibers (CNFs) and cellulose nanocrystals (CNCs) to increase the dry strength of filter paper. An application of 10% protein solution with CNCs (10:1) or CNFs (50:1) improved the elongation at break, tensile strength and modulus of treated paper products compared to the improved performance of cottonseed protein alone. Further analysis using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) indicated that the cottonseed protein/nanocellulose composites interacted with the filter paper fibers, imparting an increased dry strength. [ABSTRACT FROM AUTHOR]

Cellulosic nanomaterials are in the focus of academia and industry to realize light-weight biobased materials with remarkable strength. While the effect is well known, the distribution of these nanomaterials are less explored, particularly for paper sheets. Here, we explore the 3D distribution of micro and nanosized cellulosic particles in paper sheets and correlate their extent of fibrillation to the distribution inside the sheets and subsequently to paper properties. To overcome challenges with contrast between the particles and the matrix, we attached probes on the cellulose nano/microparticles, either by covalent attachment of fluorescent dyes or by physical deposition of cobalt ferrite nanoparticles. The increased contrast enabled visualization of the micro and nanosized particles inside the paper matrix using multiphoton microscopy, X-ray microtomography and SEM-EDX. The results indicate that fibrillary fines enrich at pores and fiber-fiber junctions, thereby increasing the relative bonded area between fibers to enhance paper strength while CNF seems to additionally form an inner 3D network. [ABSTRACT FROM AUTHOR]

Perovskite quantum dots (PQDs) are a competitive candidate for next‐generation display technologies as a result of their superior photoluminescence, narrow emission, high quantum yield, and color tunability. However, due to poor thermal resistance and instability under high energy radiation, most PQD‐based white light‐emitting diodes (LEDs) show only modest luminous efficiency of ≈50 lm W−1 and a short lifetime of <100 h. In this study, by incorporating cellulose nanocrystals, a new type of QD film is fabricated: CH3NH3PbBr3 PQD paper that features 91% optical absorption, intense green light emission (518 nm), and excellent stability attributed to the complexation effect between the nanocellulose and PQDs. The PQD paper is combined with red K2SiF6:Mn4+ phosphor and blue GaN LED chips to fabricate a high‐performance white LED demonstrating ultrahigh luminous efficiency (124 lm W−1), wide color gamut (123% of National Television System Committee), and long operation lifetime (240 h), which paves the way for advanced lighting technology. [ABSTRACT FROM AUTHOR]

Paper‐based electronics has attracted growing interest owing to many advantages of papers including low‐cost, abundance, flexibility, biocompatibility, and environmental friendliness. Despite recent progress in paper electronics, however, development of a high‐performance paper‐based triboelectric nanogenerator (TENG), which is a power‐generating device that converts mechanical energy into electric energy by coupling triboelectrification and electrostatic induction, remains a challenge mainly due to weak electron‐donating tendency of cellulose‐based papers. In this work, highly conductive ferroelectric cellulose composite papers containing silver nanowires and BaTiO3 nanoparticles are fabricated, and their successful application for realizing a large‐area TENG with enhanced electrical output performance is demonstrated. It is found that triboelectric charge generation on the ferroelectric cellulose composite paper can be promoted by simple poling treatment, which significantly enhances TENG performance. The ferroelectric cellulose composite paper–based TENG exhibits an electrical output performance that surpasses those of aluminum‐based and pristine cellulose–based TENGs by more than two times, as well as outstanding output stability without a noticeable degradation in performance during 10 000 cycles of a repeated pushing test. The work demonstrates the great potential of multifunctional cellulose‐based papers for TENG and other self‐powered electronic applications. [ABSTRACT FROM AUTHOR]