3D printing of renewable building blocks like cellulose nanocrystals offers an attractive pathway for fabricating sustainable structures. Here, viscoelastic inks composed of anisotropic cellulose nanocrystals (CNC) that enable patterning of 3D objects by direct ink writing are designed and formulated. These concentrated inks are composed of CNC particles suspended in either water or a photopolymerizable monomer solution. The shear-induced alignment of these anisotropic building blocks during printing is quantified by atomic force microscopy, polarized light microscopy, and 2D wide-angle X-ray scattering measurements. Akin to the microreinforcing effect in plant cell walls, the alignment of CNC particles during direct writing yields textured composites with enhanced stiffness along the printing direction. The observations serve as an important step forward toward the development of sustainable materials for 3D printing of cellular architectures with tailored mechanical properties.

In this work, we report the facile synthesis of hydrophobic, flexible, and ultralightweight (ρ sponge ≤ 17.3 mg/cm 3 ) nanocellulose sponges using a novel and efficient silylation process in water. These functional materials with high porosity (≥99%) are easily engineered by freeze-drying water suspensions of nanofibrillated cellulose (NFC), a natural nanomaterial isolated from renewable resources, in the presence of methyltrimethoxysilane sols of various concentrations. Microscopic and solid state nuclear magnetic resonance analyses reveal that the sponges are composed of a three-dimensional cellulosic network of thin sheets and nanofilaments, covered by polysiloxanes. Compared with conventional inorganic porous materials, the silylated NFC sponges display an unprecedented flexibility with a maximal shape recovery corresponding to 96% of the original thickness after 50% compression strain. The sponges also combine both hydrophobic and oleophilic properties and prove to be very efficient in removing dodecane spills from a water surface with an excellent selectivity and recyclability. Finally, the sponges can collect a wide range of organic solvents and oils with absorption capacities up to 100 times their own weight, depending on the density of the liquids. This versatile functionalization method opens up new opportunities for the design of novel advanced functional biomaterials with controlled properties.

A novel amine-based adsorbent for CO₂ capture from air was developed, which uses biogenic raw materials and an environmentally benign synthesis route without organic solvents. The adsorbent was synthesized through freeze-drying an aqueous suspension of nanofibrillated cellulose (NFC) and N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane (AEAPDMS). At a CO₂ concentration of 506 ppm in air and a relative humidity of 40% at 25 °C, 1.39 mmol CO₂/g was absorbed after 12 h. Stability was examined for over 20 consecutive 2-h-adsorption/1-h-desorption cycles, yielding a cyclic capacity of 0.695 mmol CO₂/g.

In the present study, novel bionanocomposite materials with tunable properties were successfully prepared using a poly(lactic acid) (PLA) matrix and acetylated microfibrillated cellulose (MFC) as reinforcing agent. The acetylation of MFC was confirmed by FTIR and (13)C CP-MAS NMR spectroscopies. The grafting of acetyl moieties on the cellulose surface not only prevented MFC hornification upon drying but also dramatically improved redispersibility of the powdered nanofibers in chloroform, a PLA solvent of low polarity. Moreover, we demonstrate that the properties of the resulting PLA nanocomposites could be tailored by adjusting both the acetyl content (Ac%) and the amount of MFC. These nanomaterials showed improved filler dispersion, higher thermal stability, and reduced hygroscopicity with respect to those prepared with unmodified MFC. Dynamic mechanical analysis (DMA) highlighted the reinforcing potential of both the unmodified and the acetylated MFC on the viscoelastic properties of the neat PLA. But more interesting, an increase in the PLA glass transition temperature was detected when using the 8.5% acetylated MFC at 17 wt %, indicating an improved compatibility at the fiber-matrix interface. These findings suggest that the final properties of nanocomposite materials can be controlled by adjusting the %Ac of MFC.

Silica aerogels are amongst the lightest mesoporous solids known and well recognized for their superinsulating properties, but the weak mechanical properties of the inorganic network structure has often narrowed their field of application. Here, the inherent brittleness of dried inorganic gels is tackled through the elaboration of a strong mesoporous silica aerogel interpenetrated with a silylated nanocellulosic scaffold. To this avail, a functionalized scaffold is synthesized by freeze‐drying an aqueous suspension of nanofibrillated cellulose (NFC)—a bio‐based nanomaterial mechanically isolated from renewable resources—in the presence of methyltrimethoxysilane sol. The silylated NFC scaffold displays a high porosity (>98%), high flexibility, and reduced thermal conductivity (λ) compared with classical cellulosic structures. The polysiloxane layer decorating the nanocellulosic scaffold is exploited to promote the attachment of the mesoporous silica matrix onto the nanofibrillated cellulose scaffold (NFCS), leading to a reinforced silica hybrid aerogel with improved thermomechanical properties. The highly porous (>93%) silica‐NFC hybrids displays meso‐ and macroporosity with pore diameters controllable by the NFCS mass fraction, reduced linear shrinkage, improved compressive properties (55% and 126% increase in Young's modulus and tensile strength, respectively), while maintaining superinsulating properties (λ ≤ 20 mW (m K)–1). This study details a new direction for the synthesis of multiscale hybrid silica aerogel structures with tailored properties through the use of alkyltrialkoxysilane prefunctionalized nanocellulosic scaffolds.

International audienceIn this article, we highlight the potential of nanocelluloses, such as cellulose nanocrystals (CNC) and microfibrillated cellulose (MFC), to serve as building blocks for the design of hierarchical functional nanomaterials. Four categories of value-added nanomaterials are envisaged here, namely aerogels, emulsions, templated materials and stimuli-responsive nanodevices. But most importantly, we demonstrate that appropriate functionalization methods are required in order to tailor the nanocellulose surface and further design materials with required characteristics

Cellulose II nanowhiskers (CNW-II) were produced by treatment of microcrystalline cellulose with sulfuric acid by both controlling the amount of H(2)SO(4) introduced and the time of addition during the hydrolysis process. The crystalline structure was confirmed by both XRD and (13)C CP-MAS NMR spectroscopy. When observed between crossed polarizers, the cellulose II suspension displayed flow birefringence and was stable for several months. The CNW-II nanowhiskers were significantly smaller than the cellulose I nanowhiskers (CNW-I) and had a rounded shape at the tip. The CNW-II average length and height were estimated by AFM to be 153 ± 66 and 4.2 ± 1.5 nm, respectively. An average width of 6.3 ± 1.7 nm was found by TEM, suggesting a ribbon-shape morphology for these whiskers. The average dimensions of the CNW-II elementary crystallites were estimated from the XRD data, using Scherrer's equation. A tentative cross-sectional geometry consistent with both XRD and NMR data was then proposed and compared with the geometry of the CNW-I nanowhiskers.

Silica aerogels are excellent thermal insulators, but their brittle nature has prevented widespread application. To overcome these mechanical limitations, silica-biopolymer hybrids are a promising alternative. A one-pot process to monolithic, superinsulating pectin-silica hybrid aerogels is presented. Their structural and physical properties can be tuned by adjusting the gelation pH and pectin concentration. Hybrid aerogels made at pH 1.5 exhibit minimal dust release and vastly improved mechanical properties while remaining excellent thermal insulators. The change in the mechanical properties is directly linked to the observed "neck-free" nanoscale network structure with thicker struts. Such a design is superior to "neck-limited", classical inorganic aerogels. This new class of materials opens up new perspectives for novel silica-biopolymer nanocomposite aerogels.