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Transparent wood composites (TWs) offer the possibility of unique coloration effects. A colored transparent wood composite (C-TW) with enhanced fire retardancy was impregnated by metal ion solutions, followed by methyl methacrylate (MMA) impregnation and polymerization. Bleached birch wood with a preserved hierarchical structure acted as a host for metal ions. Cobalt, nickel, copper, and iron metal salts were used. The location and distribution of metal ions in C-TW as well as the mechanical performance, optical properties, and fire retardancy were investigated. The C-TW coloration is tunable by controlling the metal ion species and concentration. The metal ions reduced heat release rates and limited the production of smoke during forced combustion tests. The potential for scaled-up production was verified by fabricating samples with a dimension of 180 x 100 x 1 (l x b x h) mm(3)., QC 20240116

Polymer shape-memory aerogels (PSMAs) are prospects in various fields of application ranging from aerospace to biomedicine, as advanced thermal insulators, actuators, or sensors. However, the fabrication of PSMAs with good mechanical performance is challenging and is currently dominated by fossil-based polymers. In this work, strong, shape-memory bio-aerogels with high specific surface areas (up to 220 m2/g) and low radial thermal conductivity (0.042 W/mK) were prepared through a one-step treatment of native wood using an ionic liquid mixture of [MTBD]+[MMP]−/DMSO. The aerogel showed similar chemical composition similar to native wood. Nanoscale spatial rearrangement of wood biopolymers in the cell wall and lumen was achieved, resulting in flexible hydrogels, offering design freedom for subsequent aerogels with intricate geometries. Shape-memory function under stimuli of water was reported. The chemical composition and distribution, morphology, and mechanical performance of the aerogel were carefully studied using confocal Raman spectroscopy, AFM, SAXS/WAXS, NMR, digital image correlation, etc. With its simplicity, sustainability, and the broad range of applicability, the methodology developed for nanoscale reassembly of wood is an advancement for the design of biobased shape-memory aerogels., QC 20230515

TW transparent wood/polymer biocomposite laminates are of interest as multifunctional materials with good longitudinal modulus, tensile strength and optical transmittance. The effect of filling the pore space in wood with a polymer matrix on fracture toughness and crack growth is not well understood. Here, we carried out in-situ fracture tests on neat birch wood and laminates made of four layers of delignified birch veneers impregnated with poly(methyl methacrylate) (PMMA) and investigated crack growth in the tangential-radial (TR) fracture system. Fracture toughness KIc and JIc at crack initiation were estimated, including FEM analysis. SEM microscopy revealed that cracks primarily propagate along the ray cells, but cell wall peeling and separation between the PMMA and wood phases also take place. A combination of in-situ tests and strain field measured by digital image correlation (DIC) showed twice as long fracture process zone of TW laminates compared with neat birch., QC 20230821

Optically transparent wood has been fabricated by structure-retaining delignification of wood and subsequent infiltration of thermo- or photocurable polymer resins but still limited by the intrinsic low mesopore volume of the delignified wood. Here we report a facile approach to fabricate strong transparent wood composites using the wood xerogel which allows solvent-free infiltration of resin monomers into the wood cell wall under ambient conditions. The wood xerogel with high specific surface area (260 m2 g–1) and high mesopore volume (0.37 cm3 g–1) is prepared by evaporative drying of delignified wood comprising fibrillated cell walls at ambient pressure. The mesoporous wood xerogel is compressible in the transverse direction and provides precise control of the microstructure, wood volume fraction, and mechanical properties for the transparent wood composites without compromising the optical transmittance. Transparent wood composites of large size and high wood volume fraction (50%) are successfully prepared, demonstrating potential scalability of the method., QC 20230711

Owing to the hierarchical structure, easy multi-functionalization and favorable mechanical properties, wood could harvest electricity from mechanical energy through piezoelectric behavior. In this work, a scalable method to synthesize wood/ZnO composite with multilayered ZnO morphologies is reported for efficient mechanical energy conversion. The synthesis includes charged wood template fabrication, precursor infiltration, and ZnO hydrothermal growth, resulting in controlled ZnO morphologies and distributions while maintaining the hierarchical structure of the wood. Stereo-digital image correlation (stereo-DIC) investigated the relationship between deformation and piezoelectric performance, which revealed the homogeneous distribution of multilayered ZnO enhance piezoelectric performance. The output voltage of wood/ZnO was 1.5 V under periodic mechanical compression (8–10 N) for 300 cycles, while the output current was 2.91 nA. The scalable synthesis strategy and piezoelectric performance are significant for the design of advanced wood nanocomposites for sustainable and efficient energy conversion systems., QC 20230627

Silk fibroin, a widely used natural biopolymer, presents remarkable flexibility and biodegradability, making it of great interest as a polymer matrix for functional composite materials. Herein, composites of silk nanofibrils and metal-organic framework (MOF) nanosheets were successfully fabricated by a coincubation and coassembly process. Under heat incubation, silk fibroin self-assembled into one-dimensional nanofibrils, while MOF nanosheets simultaneously covered or wrapped on the silk nanofibrils in a water suspension. Transparent composite membranes were obtained from their water suspensions by the solution casting method. The regenerated silk nanofibrils formed a network structure, and the integrated MOF nanosheets (0.1 to 3.0 wt %) endowed the composites with aggregation-induced emission luminogen (AIEgen)-based fluorescence. The fluorescence intensity of the composites was significantly enhanced owing to the interfacial interactions between silk nanofibrils and MOF nanosheets. The composite membranes also offer excellent UV shielding while maintaining optical transparency in the visible spectrum. This work provides an efficient pathway to fabricate luminescent silk protein-based composites for functional materials such as fluorescence sensing and anticounterfeiting., QC 20230704

The nature of mass transport in plants has recently inspired the development of low-cost and sustainable wood-based electronics. Herein, we report a wood electrochemical transistor (WECT) where all three electrodes are fully made of conductive wood (CW). The CW is prepared using a two-step strategy of wood delignification followed by wood amalgamation with a mixed electron-ion conducting polymer, poly(3,4-ethylenedioxythiophene)–polystyrene sulfonate (PEDOT:PSS). The modified wood has an electrical conductivity of up to 69 Sm−1 induced by the formation of PEDOT:PSS microstructures inside the wood 3D scaffold. CW is then used to fabricate the WECT, which is capable of modulating an electrical current in a porous and thick transistor channel (1 mm) with an on/off ratio of 50. The device shows a good response to gate voltage modulation and exhibits dynamic switching properties similar to those of an organic electrochemical transistor. This wood-based device and the proposed working principle demonstrate the possibility to incorporate active electronic functionality into the wood, suggesting different types of bio-based electronic devices., QC 20230713

Nacre-mimicking nanocomposites based on colloidal cellulose nanofibrils (CNFs) and clay nanoparticles show excellent mechanical properties, yet processing typically involves preparation of two colloids followed by a mixing step, which is time- and energy-consuming. In this study, a facile preparation method using low energy kitchen blenders is reported in which CNF disintegration, clay exfoliation and mixing carried out in one step. Compared to composites made from the conventional method, the energy demand is reduced by about 97 %; the composites also show higher strength and work to fracture. Colloidal stability, CNF/clay nanostructure, and CNF/clay orientation are well characterized. The results suggest favorable effects from hemicellulose-rich, negatively charged pulp fibers and corresponding CNFs. CNF disintegration and colloidal stability are facilitated with substantial CNF/clay interfacial interaction. The results show a more sustainable and industrially relevant processing concept for strong CNF/clay nanocomposites., QC 20230424

Eco-friendly materials with superior thermal insulation and mechanical properties are desirable for improved energy- and space-efficiency in buildings. Cellulose aerogels with structural anisotropy could fulfill these requirements, but complex processing and high energy demand are challenges for scaling up. Here we propose a scalable, nonadditive, top-down fabrication of strong anisotropic aerogels directly from wood with excellent, near isotropic thermal insulation functions. The aerogel was obtained through cell wall dissolution and controlled precipitation in lumen, using an ionic liquid (IL) mixture comprising DMSO and a guanidinium phosphorus-based IL [MTBD][MMP]. The wood aerogel shows a unique structure with lumen filled with nanofibrils network. In situ formation of a cellulosic nanofibril network in the lumen results in specific surface areas up to 280 m2/g and high yield strengths >1.2 MPa. The highly mesoporous structure (average pore diameter ∼20 nm) of freeze-dried wood aerogels leads to low thermal conductivities in both the radial (0.037 W/mK) and axial (0.057 W/mK) directions, showing great potential as scalable thermal insulators. This synthesis route is energy efficient with high nanostructural controllability. The unique nanostructure and rare combination of strength and thermal properties set the material apart from comparable bottom-up aerogels. This nonadditive synthesis approach is believed to contribute significantly toward large-scale design and structure control of biobased aerogels., QC 20221019

A concept of transparent “quantum dot glass”(TQDG) is proposed for a combination of a quantum dot(QD)-based glass luminescent solar concentrator (LSC) and itsedge-attached solar cells, as a type of transparent photovoltaics(TPVs) for building-integrated photovoltaics (BIPVs). Differentfrom conventional LSCs, which typically serve as pure opticaldevices, TQDGs have to fulfill requirements as both powergeneratingcomponents and building construction materials. In thiswork, we demonstrate large-area (400 cm2) TQDGs based onsilicon QDs in a triplex glass configuration. An overall powerconversion efficiency (PCE) of 1.57% was obtained with back-reflection for a transparent TQDG (average visible transmittance of84% with a color rendering index of 88 and a low haze ≤3%), contributing to a light utilization efficiency (LUE) of 1.3%, which isamong the top reported TPVs based on the LSC technology with similar size. Most importantly, these TQDGs are shown to havebetter thermal and sound insulation properties compared to normal float glass, as well as improved mechanical performance andsafety, which significantly pushes the TPV technology toward practical building integration. TQDGs simultaneously exhibit favorablephotovoltaic, aesthetic, and building envelope characteristics and can serve as a multifunctional material for the realization of nearlyzero-energy building concepts., QC 20220906

The preparation of wood substrates modified by charged inorganic nanoparticles (NPs) diffusing into the internal cell wall structure is investigated for generating functional properties. The flammability problem of wood biocomposites is addressed. NPs applied from colloidal sols carry charge to stabilize them against aggregation. The influence of charge on particle diffusion and adsorption should play a role for their spatial distribution and localization in the wood substrate biocomposite. It is hypothesized that improved dispersion, infiltration, and stability of NPs into the wood structure can be achieved by charge control diffusion, also restricting NP agglomeration and limiting distribution to the wood cell wall. Cationic and anionic silica NPs of ≈30 nm are therefore allowed to diffuse into bleached wood. The influence of charge on distribution in wood is investigated as a function of initial sol concentration. Transparent wood is fabricated by in situ polymerization of a thiol­ene in the wood pore space. These biocomposites demonstrate excellent flame retardancy with self­extinguishing characteristics. The approach has potential for commercial fabrication of flame retardant transparent composites for glazing and other building applications., QC 20220523

Nanocomposites based on components from nature, which can be recycled are of great interest in new materials for sustainable development. The range of properties of nacre-inspired hybrids of 1D cellulose and 2D clay platelets are investigated in nanocomposites with improved nanoparticle dispersion in the starting hydrocolloid mixture. Films with a wide range of compositions are prepared by capillary force assisted physical assembly (vacuum-assisted filtration) of TEMPO-oxidized cellulose nanofibers (TOCN) reinforced by exfoliated nanoclays of three different aspect ratios: saponite, montmorillonite and mica. X-ray diffraction and transmission electron micrographs show almost monolayer dispersion of saponite and montmorillonite and high orientation parallel to the film surface. Films exhibit ultimate strength up to 573 MPa. Young's modulus exceeds 38 GPa even at high MTM contents (40-80 vol%). Optical transmittance, UV-shielding, thermal shielding and fire-retardant properties are measured, found to be very good and are sensitive to the 2D nanoplatelet dispersion., QC 20220325

Composite polymer hydrogels are of significant interests for high optical transparency and mechanical performance. In this work, a strong and transparent composite hydrogel is developed from a highly mesoporous cellulose network prepared from wood via top-down delignification followed by TEMPO-mediated oxidation and in situ polymerization of PNIPAM. Individualization of cellulose microfibrils inside the wood cell wall is critical for the fabrication of free-standing composite hydrogel with high water content of 94.9 wt% and high optical transmittance of 85.8% with anisotropic light scattering behavior. The composite hydrogel also showed anisotropic mechanical properties with a tensile strength, Young's modulus and toughness of 317 kPa, 5.4 MPa, and 39.2 kJ m- 3 in axial direction, and 152 kPa, 0.31 MPa and 57.1 kJ m- 3 in the transverse direction, respectively. It also showed thermochromic behavior, i.e., reversibly changing between transparent and brightly white by a temperature change between 25 and 40 degrees C, demonstrating great potential for optical applications., QC 20220120

Hot-pressed, binder-free wood fiber (WF) composites can serve as load-bearing and eco-friendly materials, and the comparison of nanoscale fibril reinforcement with microscale wood fibers is of interest. We investigated property differences and interpreted deformation mechanisms with strain field measurements using digital image correlation combined with orthotropic, elastic–plastic finite element model updating predictions. Random-in-plane microfibrillated lignocellulose (MFLC) composites showed better mechanical properties than WF composites due to stronger strain-hardening from lower porosity and better interfibrillar adhesion, provided by the intrinsic lignin-hemicellulose binder. Axially oriented wood fiber composites (O-WF) achieved comparable mechanical properties to random MFLC, with lower values for eco-indicators. The FEM updating method could successfully determine all 4 independent elastic constants from one 45° off-axis experiment, although the plasticity model required two more experiments., QC 20220824

Water-processed nanocomposites based on cellulose nanofibrils (CNF and 2D platelets are sustainable alternatives to nanocomposites from fossil-based polymers. The degree of dispersion of 2D platelets in CNF matrix is critical to mechanical properties, but reduced graphene oxide (RGO) has poor hydrocolloidal stability. This is addressed by forming electrically conductive and strong CNF-RGO nanocomposites by green chemical reduction of wet, vacuum-filtered CNF-GO cakes, taking advantage of the colloidal dispersibility of GO platelets in CNF, as characterized in the solid nanocomposite by SAXS, WAXS and FE-SEM. CNF-RGO nanocomposite with 2 wt% RGO shows a Youngs modulus of 20.4 GPa and tensile strength of 319 MPa, with considerable ductility at 50 % RH. Although CNF-GO shows much higher moisture sorption than CNF-RGO at 90 %RH, the CNF-GO mechanical properties are higher, for thermodynamic reasons, MD simulations predict dry, hydrogen-bonded CNF-GO interfaces even in wet conditions, and this can explain the better performance of CNF-GO., QC 20221128

This review paper provides a recent overview of current international research that is being conducted into the functional properties of cellulose as a nanomaterial. A particular emphasis is placed on fundamental and applied research that is being undertaken to generate applications, which are now becoming a real prospect given the developments in the field over the last 20 years. A short introduction covers the context of the work, and definitions of the different forms of cellulose nanomaterials (CNMs) that are most widely studied. We also address the terminology used for CNMs, suggesting a standard way to classify these materials. The reviews are separated out into theme areas, namely healthcare, water purification, biocomposites, and energy. Each section contains a short review of the field within the theme and summarizes recent work being undertaken by the groups represented. Topics that are covered include cellulose nanocrystals for directed growth of tissues, bacterial cellulose in healthcare, nanocellulose for drug delivery, nanocellulose for water purification, nanocellulose for thermoplastic composites, nanocellulose for structurally colored materials, transparent wood biocomposites, supercapacitors and batteries., QC 20221123

While strong water association with cellulose in plant cell walls and man-made materials is well-established, its molecular scale aspects are not fully understood. The thermodynamic consequences of having water molecules located at the microfibril-microfibril interfaces in cellulose fibril aggregates are therefore analyzed by molecular dynamics simulations. We find that a thin layer of water molecules at those interfaces can be in a state of thermal equilibrium with water surrounding the fibril aggregates because such an arrangement lowers the free energy of the total system. The main reason is enthalpic: water at the microfibril- microfibril interfaces enables the cellulose surface hydroxyls to experience a more favorable electrostatic environment. This enthalpic gain overcomes the entropic penalty from strong immobilization of water molecules. Hence, those particular water molecules stabilize the cellulose fibril aggregates, akin to the role of water in some proteins. Structural and functional hypotheses related to this finding are presented., QC 20230328

Transparent wood (TW) biocomposites combine high optical transmittance and good mechanical properties and can contribute to sustainable development. The safety against fire is important for building applications. Here, a "green" bleached wood reinforcement is impregnated by water soluble and flame-retardant melamine formaldehyde (MF) in a scalable process, for a wood content of 25 vol%. FE-SEM is used for characterization of optical defects and EDX to examine MF distribution at nanoscale cell wall pore space. Curing (FTIR-ATR), mechanical properties, optical transmittance (74% at 1.2 mm thickness) and flame-retardant properties are also characterized (self-extinguishing behavior and cone calorimetry), and scattering mechanisms are discussed. The fire growth rate of transparent wood was less than half the values for neat wood. Transparent wood/MF biocomposites show interesting wood-MF synergies and are of practical interest in building applications. Critical aspects of processing are analyzed for minimization of optical defects., QC 20220530

Nacre-like materials have been extensively studied in the literature for different material system due its capability of balancing strength and toughness [1]. In this material system, weak interfaces between inclusions and matrices are key to allow the crack deflection, and thus, higher toughness is achieved. Over a decade our research group have been able to reproduce nacre-like nanostructure on cellulosic papers as matrix, and montmorillonite clay as nano platelets inclusions [2, 3]. Apart of good functionally in our material system, such as transparency, fire retardance and gas barrier functions, we have also finetuned its recyclability in recent findings. Our objective now is to understand better what is failure mechanism that control our nanostructure and how we can predict the mechanical performance in terms of stiffness, strength and toughness in the macroscopic level.In this presentation, we are going to show micromechanical modelling to estimate the composite modulus of this novel biocomposite, and compare the results to numerical predictions and experimental measurements. Furthermore, we will present our efforts in an atomistic-continuum modelling framework to predict strength and toughness for our nano composite. First, molecular dynamics simulations are performed on our cellulose nanofibrils (CNF) to obtain the stress-strain curve in order to calibration the continuum model. Then, the continuum model containing the calibrated phase field model for fracture in the CNF matrix, and calibrated cohesive zone model at the interfaces will be explored to predict the failure. The advantages and disadvantages of our framework will be addressed, as well as the accuracy of the assumptions in their underlying models. REFERENCES 1. Barthelat, F., Architectured materials in engineering and biology: fabrication, structure, mechanics and performance. International Materials Reviews, 2015. 60(8): p. 413-430. 2. Liu, A., et al., Clay Nanopaper with Tough Cellulose Nanofibe, QC 20230825

Cellulose nanocomposites from cellulose nanofibrils (CNF) has now become a de facto candidate for structural purpose due its good mechanical properties [1]. Unlike synthetic composites, cellulosic composites have advantage of being more cyclable and/or biodegradable [2], in which it is aligned towards the immediate need for sustainable solutions. One branch in the portfolio of cellulose-based materials is the transparent nacre-inspired nanocomposites. Such composites are normally thin films made of fairly uniform CNF matrix with random orientation of fibres, and of montmorillonite (MTM) natural clay as nano inclusions [2, 3]. The MTM inclusions have a plate like-shaped with diameter of roughly 100-400 nm and height of 1-15 nm, and are very well in- plane orientated. Along the thickness of the films, the nanocomposite owns a brick-and-mortar microstructure (please see Figure 1 (a)). This complex nano-microstructure leads to difficulties in predicting the mechanical properties, and that is the main reason those are mainly experimentally measured. In this work, we propose a simplified 2D representative unit cell (UC) of the nanocomposite, shown in Figure 1(b), to understand the porosity detrimental effect in the in-plane elastic modulus of the nanocomposite seen in the ordinary tensile testing. The porous UC has been idealized from experimental observation in the previous studies (e.g. microscopy imaging), and was used in the computation homogenization setting to estimate the effective in-plane elastic modulus of the nanocomposite, and to analyse the stress distribution in the UC. Preliminary results in Figure 2 show that the UC has been able to capture the experimental trend, which is the thicker platelets the lower is the elastic modulus of the composite. More details, such as material modelling, input parameters, comparison with experiments will be discussed in the presentation, as well as advantages and limitations of the study. References [1] Berglund, L.A., Peijs, QC 20230825

Nanostructured wood veneer with added electroactive functionality combines structural and functional properties into eco-friendly, low-cost nanocomposites for electronics and energy technologies. Here, we report novel conducting polymer-impregnated wood veneer electrodes where the native lignin is preserved, but functionalized for redox activity and used as an active component. The resulting electrodes display a well-preserved structure, redox activity, and high conductivity. Wood samples were sodium sulfite-treated under neutral conditions at 165 °C, followed by the tailored distribution of PEDOT:PSS, not previously used for this purpose. The mild sulfite process introduces sulfonic acid groups inside the nanostructured cell wall, facilitating electrostatic interaction on a molecular level between the residual lignin and PEDOT. The electrodes exhibit a conductivity of up to 203 S m−1 and a specific pseudo-capacitance of up to 38 mF cm−2, with a capacitive contribution from PEDOT:PSS and a faradaic component originating from lignin. We also demonstrate an asymmetric wood pseudo-capacitor reaching a specific capacitance of 22.9 mF cm−2 at 1.2 mA cm−2 current density. This new wood composite design and preparation scheme will support the development of wood-based materials for use in electronics and energy storage., QC 20230614

Wood pulp fibres are promising reinforcements for biocomposites due to their renewable resource origin and mechanical properties. An oriented and dense fibre reinforcement structure is beneficial for biocomposite properties. We present a method of modifying fibres (e.g. to increase strain to failure) in pre-formed oriented high-density paper structures intended for biocomposites or as hot-pressed fibre materials. Mildly delignified, well-preserved holocellulose fibres from softwood are used. Cold alkali treatment (hemicellulose removal) and mercerisation (conversion to cellulose II) were carried out successfully on oriented fibre sheets. Controlled anisotropy and sheet density are achieved from untreated and straight fibres in the sheet formation step. High mechanical properties and increased ductility of mercerised sheets were observed, which may be valuable for hot-pressed fibre materials (E ≈ 7.1 GPa, strength of 108 MPa and strain to failure of 5.3%) and biocomposites. In contrast, modified wood pulp fibres were difficult to orient, resulting in higher sheet porosity and weak interfibre bonding., QC 20230524

Functional wood materials often rely on active additives due to the weak piezoelectric response of wood itself. Here, we chemically modify wood to form functionalized, eco-friendly wood veneer for self-powered vibration sensors. Only the piezoelectricity of the cellulose microfibrils is used, where the drastic improvement comes only from molecular and nanoscale wood structure tuning. Sequential wood modifications (delignification, oxidation, and model fluorination) are performed, and effects on vibration sensing abilities are investigated. Wood veneer piezoelectricity is characterized by the piezoresponse force microscopy mode in atomic force microscopy. Delignification, oxidation, and model fluorination of wood-based sensors provide output voltages of 11.4, 23.2, and 60 mV by facilitating cellulose microfibril deformation. The vibration sensing ability correlates with improved piezoelectricity and increased cellulose deformation, most likely by large, local cell wall bending. This shows that nanostructural wood materials design can tailor the functional properties of wood devices with potential in sustainable nanotechnology., QC 20230524

Transparent wood (TW)-based composites are of significant interest for smart window applications. In this research, we demonstrate a facile dual-stimuli-responsive chromic TW where optical properties are reversibly controlled in response to changes in temperature and UV-radiation. For this functionality, bleached wood was impregnated with solvent-free thiol and ene monomers containing chromic components, consisting of a mixture of thermo- and photoresponsive chromophores, and was then UV-polymerized. Independent optical properties of individual chromic components were retained in the compositional mixture. This allowed to enhance the absolute optical transmission to 4 times above the phase change temperature. At the same time, the transmission at 550 nm could be reduced 11−77%, on exposure to UV by changing the concentration of chromic components. Chromic components were localized inside the lumen of the wood structure, and durable reversible optical properties were demonstrated by multiple cycling testing. In addition, the chromic TW composites showed reversible energy absorption capabilities for heat storage applications and demonstrated an enhancement of 64% in the tensile modulus as compared to a native thiol−ene polymer. This study elucidates the polymerization process and effect of chromic components distribution and composition on the material’s performance and perspectives toward the development of smart photoresponsive windows with energy storage capabilities., QC 20210201

The development of large, multifunctional structures from sustainable wood nanomaterials is challenging. The need to improve mechanical performance, reduce moisture sensitivity, and add new functionalities, provides motivation for nanostructural tailoring. Although existing wood composites are commercially successful, materials development has not targeted nano-structural control of the wood cell wall, which could extend the property range. For sustainable development, non-toxic reactants, green chemistry and processing, lowered cumulative energy requirements, and lowered CO2-emissions are important targets. Here, modified wood substrates in the form of veneer are suggested as nanomaterial components for large, load-bearing structures. Examples include polymerization of bio-based monomers inside the cell wall, green chemistry wood modification, and addition of functional inorganic nanoparticles inside the cell wall. The perspective aims to describe bio-based polymers and green processing concepts for this purpose, along with wood nanoscience challenges., QC 20210803

The sustainable development of engineering biocomposites has been limited due to a lack of bio‐based monomers combining favorable processing with high performance. Here, the authors report a novel and fully bio‐based transparent wood biocomposite based on green synthesis of a new limonene acrylate monomer from renewable resources. The monomer is impregnated and readily polymerized in a delignified, succinylated wood substrate to form optically transparent biocomposites. The chemical structure of the limonene acrylate enables diffusion into the cell wall, and the polymer phase is both refractive index‐matched and covalently linked to the wood substrate. This results in nanostructured biocomposites combining an excellent optical transmittance of 90% at 1.2 mm thickness and a remarkably low haze of 30%, with a high mechanical performance (strength 174 MPa, Young's modulus 17 GPa). Bio‐based transparent wood holds great potential towards the development of sustainable wood nanotechnologies for structural applications, where transparency and mechanical performance are combined., QC 20210524

Fire resistance testing of components made of carbon fibre reinforced polymers (CFRP) usually demands intermediate-scale or full-scale testing. A bench-scale test is presented as a practicable and efficient method to assess how different fire protective systems improve the structural integrity of CFRPs during fire. The direct flame of a fully developed fire was applied to one side of the CFRP specimen, which was simultaneously loaded with compressive force. Three different approaches (film, non-woven, and coatings) were applied: paper with a thickness in the range of mu m consisting of cellulose nanofibre (CNF)/clay nanocomposite, nonwoven mats with thickness in the range of cm and intumescent coatings with a thickness in the range of mm. The uncoated specimen failed after just 17 s. Protection by these systems provides fire stability, as they multiply the time to failure by as much as up to 43 times. The reduced heating rates of the protected specimens demonstrate the reduced heat penetration, indicating the coatings' excellent heat shielding properties. Bench-scale fire stability testing is shown to be suitable tool to identify, compare and assess different approaches to fire protection., QC 20211025

Wood is an eco-friendly and abundant substrate and a candidate for functionalization by large-scale nanotechnologies. Infiltration of nanoparticles into wood, however, is hampered by the hierarchically structured and interconnected fibers in wood. In this work, delignified wood is impregnated with gold and silver salts, which are reduced in situ to plasmonic nanoparticles via microwave-assisted synthesis. Transparent biocomposites are produced from nanoparticle-containing wood in the form of load-bearing materials with structural color. The coloration stems from nanoparticle surface plasmons, which require low size dispersity and particle separation. Delignified wood functions as a green reducing agent and a reinforcing scaffold to which the nanoparticles attach, predesigning their distribution on the surface of fibrous "tubes". The nanoscale structure is investigated using scanning transmission electron microscopy (STEM), energy-dispersive spectroscopy (EDS), and Raman microscopy to determine particle size, particle distribution, and structure-property relationships. Optical properties, including response to polarized light, are of particular interest., QC 20210802

Dense polymeric films based on network-forming cellulose nanofibrils (CNFs) have excellent mechanical properties but are limited by moisture sensitivity. Here, interfibrillar effects from CNF surface properties are investigated. TEMPO-oxidized CNFs and two native CNFs are prepared with a similar length and width, to exclude geometrical effects. The CNFs have different surface properties in terms of sorbed hemicellulose content, hemicellulose molar mass, and surface charge. Moisture sorption, structural changes, and mechanical properties at different relative humidities are characterized. The presence of sorbed hemicelluloses in the interfibrillar interphase has favorable effects on the mechanical tensile properties. Surface-charged carboxyls increased moisture sorption and film thickness swelling and reduced the mechanical properties. A comparison with biaxially oriented polyethylene terephthalate films provides a perspective into the structure and properties of CNF films. The present study shows the importance of the interfibrillar interface and interphase region for mechanical film properties, including moisture effects., QC 20210614

2,2,6,6-Tetramethylpiperidin-1-yl oxyl (TEMPO)-oxidized beta-chitin nanofibrils (T-ChNF) are novel nanofibrils of high strength and stiffness and can also enhance the adsorption of chitosan in materials for biomedical applications. This study presents the preparation, structure, and properties of T-ChNF based on squid pens. Our nanofibrils have a zeta potential of -25.3 mV at neutral pH and a carboxylic content of 0.17 mmol/g, making hydrocolloid suspension stable at alkaline and neutral pH. It was demonstrated that positively charged chitosan could be adsorbed on the negatively charged surface of T-ChNF, leading to charge neutralization. The key to strong squid pen T-ChNF is the initial raw squid chitin properties and the high degree of acetylation (DA = 99.9%). The T-ChNF diameter is similar to 4.4 nm, and the length is in the micrometer range. The length and diameter are similar to those of squid pen beta-chitin fibrils prepared under mild conditions. These qualities of fibrils resulted in high-strength (176 MPa) chitin films prepared using the rapid vacuum filtration and drying technique. T-ChNF-based films are ductile, flexible, and transparent., QC 20210601

Holocellulose fibers produced by mild delignification form strong fiber networks, without beating or dry-strength agents. Recently, sequential batch delignification using peracetic acid (PAA) on finely cut wood sticks resulted in high-quality holocellulose fibers. Here, single step PAA delignification is developed for wood chips, which is simpler and can be used for larger fiber batches (400 g) with similar, high yield (60%). Such fibers have 1.4% lignin, 25% hemicelluloses content and well-preserved cellulose and hemicellulose molar mass. The corresponding paper sheet materials with a porosity of ~ 50%, have a Young’s modulus of 9 GPa and a strength of 90 MPa. Holocellulose fibers can now be readily investigated for use in larger scale paper, molded fiber and polymer biocomposite materials applications, or for cellulose nanofibril preparation., QC 20210415

Olive stone is an important biomaterial waste product generated in large amount. As a lignocellulose material, olive stone could be a sustainable resource for biosorbents. In this work, olive stone powder delignification using sodium chlorite (NaClO2) was performed to enhance metal ion adsorption capacity. The influence of the treatment on olive stone powder physical-chemical properties was studied, including specific surface area, surface chemistry, morphology, etc. The white, delignified olive stone powder was applied for metal ions (Fe3+, Cu2+, and Zn2+) adsorption. Olive stone delignification not only increases the accessibility of the olive stone powder but also broadens the applications to materials design with optical functions by the generation of a white powder., QC 20210326

Unbleached lignocellulosic wood fiber materials of low porosity are of great interest as eco-friendly load-bearing materials because their yield is much higher than that for "pure" wood cellulosics. The difference between comparable materials based on lignocellulose fibers or nanocellulose is investigated. The structure, surface area, mechanical properties, moisture sorption, and optical properties of films based on fibers or microfibrillated lignocellulose (MFLC) were characterized as a function of lignin content, and the environmental impact was compared. The modulus and tensile strength of comparable fiber and MFLC films (approximate to 25% porosity) increased up to an optimum lignin content (11-17%) and then decreased at a very high lignin content. Hot-pressed MFLC films with little porosity showed excellent properties, 230-260 MPa strength, 17-20 GPa modulus, and 81 MPa wet strength. The mechanical property values of hot-pressed wood fibers with 25% porosity were also as high as 154 MPa strength and 13.2 GPa modulus, which are higher than those of comparable materials reported in the literature. Because hot-pressed lignocellulose fibers can be readily recycled and show low cumulative energy demand, they are candidates for semistructural engineering materials. MFLC is of great interest for coatings, films, adhesives, and as additives or in high-technology applications., QC 20210325

Lightweight polymer foams from synthetic polymers are commonly used in a wide-spread spectrum of application fields. Their intrinsic flammability coupled with restrictions on flame retardant chemicals poses a severe threat to safety. Here, fire resistant foams comprising biobased components capable of replacing petroleum-based foams are investigated. Cellulose nanofibers are combined with 2D montmorillonite nanoplatelets and a native xyloglucan hemicellulose binder, using a water-based freeze casting approach. Due to the silicate nanoplatelets, these lightweight foams self-extinguish the flame during flammability tests. The limiting oxygen index is as high as 31.5% and in the same range as the best fire-retardant synthetic foams available. In cone calorimetry, the foams display extremely low combustion rates. Smoke release is near the detection limit of the instrument. In addition, the foams are withstanding the penetration of a flame torch focused on one side of the specimen (T on surface 800 °C) and structural integrity is maintained. At the same time, the unexposed side is insulated, as demonstrated by a through-thickness temperature drop of 680 °C cm−1. The results represent a tremendous opportunity for the development of fire-safe foams combining excellent sustainability with multifunctional performance., QC 20220810

Transparent wood (TW), a biocomposite material demonstrating optical transparency in the visible range, has attracted much interest in recent years due to great potential for ecofriendly applications, for instance, in construction industry and functionalized organic materials. Optical properties of TW, including transparency and haze, depend on a particular structure of cellulose-based backbone compound, (mis-)matching of the refractive indices (RIs) between TW compounds, and the polymer matrix. Although there are data of cellulose RIs for various forms of cellulose (fibers, powder, hot-pressed films, etc.), these values might differ from an effective RI of the TW substrate. Herein, a numerical model of light propagation in the TW, based on the real cellular structure in wood, is presented and applied to estimate an effective RI of the delignified wood reinforcement in the experimentally investigated TW material. Ray-tracing and rigorous electromagnetic approaches are compared for modeling light propagation in the TW. Ray tracing demonstrates considerably simplified yet accurate and efficient solutions. The work brings substantial progress toward realistic and practical wood modeling for the purpose of applications, materials design, and fundamental studies., QC 20230511

Part of book ISBN 978-311061938-6 978-311061950-8QC 20230615

Transparent wood (TW) is an interesting polymer biocomposite with potential for buildings and photonics applications. TW materials need to be eco-friendly and readily processed with few defects, for high optical transmittance and low transmission scattering at wide angles (haze). Two wood templates with different lignin-content are impregnated with a new thiol-ene thermoset system. The more eco-friendly bleached wood template results in transparent wood with high optical transmission and much reduced transmission haze, due to strong reduction of interfacial air gaps. Characterization includes template composition, thiol-ene distribution, and polymerization in wood cell wall by EDX and confocal Raman microscopy, also NMR and DSC, tensile testing and FE-SEM fractography for morphology and wood/thiol-ene interface adhesion assessment. The wood template is a true nanocomposite with thiol-ene polymer located inside the nanoporous wood cell wall. Advanced TW applications require not only appropriate wood template modification and careful polymer matrix selection but also tailoring of the process to impregnation and polymerization mechanisms, in order to reduce optical defects., QC 20201229

Highly porous, strong aerogels with anisotropicstructural properties are of great interest for multifunctionalmaterials for applications including insulators in buildings,filters for oil cleanup, electrical storage devices,etc. Contem-porary aerogels are mostly extracted from fossil resources andsynthesized from bottom-up techniques, often requiring addi-tional strategies to obtain high anisotropy. In this work, auniversal approach to prepare porous, strong, anisotropicaerogels is presented through exploiting the natural hierarchicaland anisotropic structure of wood. The preparation comprisesnanoscale removal of lignin, followed by dissolution−regener-ation of nanofibers, leading to enhanced cell wall porosity with nanofibrillated networks occupying the pore space in thecellular wood structure. The aerogels retain structural anisotropy of natural wood, exhibit specific surface areas up to 247 m2/g, and show high compression strength at 95% porosity. This is a record specific area value for wood aerogels/foams and evenhigher than most cellulose-based aerogels for its assigned strength. The aerogel can serve as a platform for multifunctionalcomposites including scaffolds for catalysis, gas separation, or liquid purification due to its porous matrix or as binder-freeelectrodes in electronics. To demonstrate the multifunctionality, the aerogels are successfully decorated with metalnanoparticles (Ag) and metal oxide nanoparticles (TiO2)byin situsynthesis, coated by the conductive polymer(PEDOT:PSS), and carbonized to yield conductive aerogels. This approach is found to be a universal way to prepare highlyporous anisotropic aerogels., QC 20200918

The α-chitin nanofibril is an alternative to nanocellulose as a building-block for strong films and other nanomaterials. The hypothesis of high film strength for films based on mildly treated insect cuticles was tested. Fibrils from the cuticle of Ruspolia differens (a long-horned bush cricket grasshopper locally known as senene) are disintegrated by a mild process, subsequently characterized by transmission electron microscopy, NMR, Fourier transform infrared spectroscopy, and XRD, and used to prepare strong and transparent films. A mild process (with 20% NaOH treatment for 2 weeks and at room temperature) was used to largely remove the strongly bound protein associated with chitin. The purpose was to reduce chitin degradation. The native structure of chitin was indeed well preserved and close to the native state, as is supported by data for degree of acetylation, molar mass, crystallinity, and crystallite dimensions. The diameter of the smallest chitin fibrils was as small as 3-7 nm (average 6 nm) with lengths larger than or around 1 μm. A stable and well-dispersed colloidal chitin fibril suspension in water was achieved. A nanostructured chitin film prepared by filtration showed high optical transmittance (∼90%) and very high tensile strength (220 MPa). The high tensile strength was attributed to the well-preserved chitin structure, high intrinsic fibril strength, and high colloidal stability of the fibril suspension. Strong, transparent insect chitin films offer interesting alternatives to nanocellulose films because of different resource origins, surface chemistries, and potential antimicrobial properties., QC 20200409

Industrial production of low-charge microfibrillated cellulose (MFC) typically results in wide fibril size distributions. This polydispersity influences viscosity, overall colloidal stability, and rheological properties of MFC suspensions and gels in aqueous systems. In this work, a systematic rheological analysis is performed for industrially prepared MFC and fractions of different size distributions. Gel formation and flow characteristics (e.g., shear-thinning) of each fraction are examined under neutral and acidic conditions and compared with the unfractionated MFC suspension. The effects of size, aspect ratio, and surface charge on the rheology of semi-dilute MFC suspensions are discussed. The results demonstrate that particle size and aspect ratio distribution control the viscoelasticity and shear-thinning properties of MFC suspensions. An increased fraction of small diameter nanofibrils, by ex situ addition of the fine particles with high aspect ratio or removal of the coarsest particles (with lower aspect ratio) by fractionation, significantly enhances the storage modulus and the yield stress of the complex mixture, compared to the properties of the coarser fractions. New insights are also reported on the tailoring of the rheology of highly polydisperse fibrillar mixtures, where the rheological contributions of each fraction are discussed. Graphic abstract: [Figure not available: see fulltext.]., QC 20201201

Chemical wood cellulose fiber modification is performed with the purpose to improve compatibility and induce nanofibrillation of fibers during melt compounding of thermoplastic biocomposites. Compounding of well-dispersed cellulose nanocomposites based on biodegradable polymers is challenging and commonly requires separate processes for wood fiber fibrillation into cellulose nanofibrils (CNF), followed by compounding. Here, nanostructured biocomposites based on poly(caprolactone) (PCL) and holocellulose wood fibers (HC) were melt compounded in a single step. Prior to compounding, PCL was grafted from the HC fibers by ring-opening polymerization (ROP) of epsilon CL with three different polymer graft lengths. The grafting was performed by two different methods: the commonly used bulk method and a new approach using acetic acid (AcOH) as the reaction solvent to swell the fiber structure during grafting. Remarkably, AcOH as a swelling solvent resulted in high density of grafts inside the nanostructure and throughout the volume of the HC wood cellulose fibers. As a consequence, more pronounced defibrillation of fibers into CNF during compounding as well as more uniform CNF dispersion in the thermoplastic PCL matrix was observed. In contrast, fibers grafted under bulk conditions showed little grafting and weak reinforcement effects. The Young's modulus and strength of the PCL were improved by almost 60% with the addition of only S wt % fibers, and the toughness was improved by 67%. The results show a close connection between the graft structure and final material properties., QC 20201014

Ramie is a plant whose fibers are used in fabrics. Ramie films are prepared by hot pressing and studied with transmission Mueller-matrix ellipsometry, which provides a complete description of polarizing and depolarizing sample properties. Symmetries of the Mueller matrices imply that the ramie films are linearly birefringent and act as waveplates. The linear birefringence is quantified by the differential decomposition of the Mueller matrices and the materials’ birefringence is found to be of the order of 0.05–0.08 with small dispersion in the visible spectral range. The films exhibit depolarization, which is quantified in terms of the depolarization index and varies from 0.9 in the infrared to 0.25 in the ultraviolet range. The deep understanding of ramie films’ polarization properties will pave the way for applications in optical and photonic devices., QC 20220322

Nanocellulose-based materials and nanocomposites show extraordinary mechanical properties with high stiffness, strength, and toughness. Although the last decade has witnessed great progress in understanding the mechanical properties of these materials, a crucial challenge is to identify pathways to introduce high wet strength, which is a critical parameter for commercial applications. Because of the waterborne fabrication methods, nanocellulose-based materials are prone to swelling by both adsorption of moist air or liquid water. Unfortunately, there is currently no best practice on how to take the swelling into account when reporting mechanical properties at different relative humidity or when measuring the mechanical properties of fully hydrated materials. This limits and in parts fully prevents comparisons between different studies. We review current approaches and propose a best practice for measuring and reporting mechanical properties of wet nanocellulose-based materials, highlighting the importance of swelling and the correlation between mechanical properties and volume expansion., QC 20200715

Materials design of efficient electrochemical micro-reactors is challenging, although hierarchically structured, self-standing electrodes with catalyst arrays offer promise. Herein, catalyst function in compact micro-reactor electrodes is designed by nanostructural tailoring of carbonized wood for efficient water splitting. Specifically, NiFe rod tipped, N-doped graphitic carbon nanocapsule arrays are self-assembled in hierarchical wood, and the benefit of this unique presentation and its promotive effect on accessibility of the catalyst surfaces is apparent. This report also comprises the first wood based micro-reactor electrodes for electrocatalytic water oxidation demonstrating excellent performance. The overpotential for oxygen evolution reaction was as low as 180 mV for 10 mA cm−2 current density and TOFredox was high at a level of 5.8 s−1 (at 370 mV overpotential). This hierarchical electrode can also work as bifunctional catalyst (both as anodic and as cathodic electrode) for total water splitting with a cell potential of 1.49 V for 10 mA cm−2 in alkaline solution, suggestive of their potential also in other electrochemical applications., QC 20200304

Transparent wood (TW) based on delignified birch veneer and thermoplastic poly(methyl methacrylate) (PMMA) is investigated by uniaxial tensile tests and full-field strain analyses based on digital image correlation techniques. TW is considered as a composite of unidirectional fibers (wood veneer) in a matrix (PMMA). Four in-plane elastic constants along the material axes are reported to enable the usage of continuum mechanics and lamination theory. Longitudinal composite strength is as high as 270 MPa at a reinforcement content of only 25 vol%. The failure behavior is interpreted based on strain field development. Strong reinforcement effects were observed from delignified birch veneer. Despite the fragility of delignified veneers, this constituent provides unexpectedly high reinforcement due to the high cellulose content and favorable stress transfer mechanisms., QC 20200518

Here we investigate the relationship between thermomechanical properties and chemical structure of well-characterized lignin-based epoxy resins. For this purpose, technical lignins from eucalyptus and spruce, obtained from the Kraft process, were used. The choice of lignins was based on the expected differences in molecular structure. The lignins were then refined by solvent fractionation, and three fractions with comparable molecular weights were selected to reduce effects of molar mass on the properties of the final thermoset resins. Consequently, any differences in thermomechanical properties are expected to correlate with molecular structure differences between the lignins. Oxirane moieties were selectively introduced to the refined fractions, and the resulting lignin epoxides were subsequently cross-linked with two commercially available polyether diamines (Mn = 2000 and 400) to obtain lignin-based epoxy resins. Molecular-scale characterization of the refined lignins and their derivatives were performed by 31P NMR, 2D-NMR, and DSC methods to obtain the detailed chemical structure of original and derivatized lignins. The thermosets were studied by DSC, DMA, and tensile tests and demonstrated diverse thermomechanical properties attributed to structural components in lignin and selected amine cross-linker. An epoxy resin with a lignin content of 66% showed a Tg of 79 °C from DMA, Young's modulus of 1.7 GPa, tensile strength of 66 MPa, and strain to failure of 8%. The effect of molecular lignin structure on thermomechanical properties was analyzed, finding significant differences between the rigid guaiacyl units in spruce lignin compared with sinapyl units in eucalyptus lignin. The methodology points toward rational design of molecularly tailored lignin-based thermosets., QC 20200617

Recyclable biocomposites based on degradable polymer systems and cellulosic plant fibers are attractive in a sustainable society, because of enhanced polymer properties and also from an end-of-life perspective. Improved understanding is required for how the degradable polymer matrix is affected during compounding in addition to effects from the cellulosic fiber structure and its chemical nature. This work reveals that a poly(ϵ-caprolactone) matrix undergoes localized, heterogeneous polymer degradation in the fiber-matrix interphase region during melt-compounding. The extent of localized degradation correlates with the initial moisture content in the wood cellulose fiber, where moisture content is controlled by different fiber modification methods by PCL-grafting. As an effect, high moisture content results in a destabilized and degraded fiber-matrix interphase. This was found through careful analysis of how the polymer population changed after compounding, using two different methods: molar mass distribution from SEC and end-group concentration from NMR. The results are important not only with regard to fiber/matrix interface compatibility but also to understand fiber modification for improved biocomposites recycling., QC 20200612

Chemical modification of wood cellulose fibers is important for tailored wood-polymer interfaces, reduced moisture sorption, and novel grades of chemical wood pulp. The present study shows how the reaction solvent system influences hydroxyl accessibility during chemical fiber modification. Surface initiated ring-opening polymerization of e-caprolactone from wood cellulose fibers was investigated in a wide range of solvent systems. The hydrogen bond donor strength of the solvent increased graft density and the amount of grafted polycaprolactone (PCL) on the fiber surface, and on nanoscale fibrils inside the fiber. Specifically, the reaction system with acetic acid as a new, green solvent for cellulose grafting increased graft density 24 times compared to bulk polymerization conditions. The results show relationships between solvent properties, hydroxyl accessibility, and grafting results in cellulosic plant fibers. The study clarifies the opportunities provided by controlling the interior of the cellulosic plant fiber cell wall during chemical modification so that the fiber becomes a swollen cellulose nanofibril gel., QC 20200310

Cellulose nanofibrils (CNFs) show high modulus and strength and are already used in industrial applications. Mechanical properties of neat CNF films or CNF-polymer matrix nanocomposites are usually much better than for polymer matrix composite films reinforced by clay, graphene, graphene oxide, or carbon nanotubes. In order to obtain small CNF diameter and colloidal stability, chemical modification has so far been necessary, but this increases cost and reduces eco-friendly attributes. In this study, an unmodified holocellulose CNF (Holo-CNF) with small diameter is obtained from mildly peracetic acid delignified wood fibers. CNF is readily defibrillated by low-energy kitchen blender processing. The hemicellulose coating on individual fibrils in the wood plant cell wall is largely preserved in Holo-CNF. This "native" CNF shows well-preserved native fibril structure in terms of length (similar to 2.1 mu m), diameter (<5 nm), high crystallinity, high cellulose molar mass, electronegative charge, and limited mechanical processing damage. The hemicellulose coating contributes mechanical properties and high optical transmittance for CNF nanopaper, which can otherwise only be achieved with chemically modified CNFs. The CNF nanopaper shows superior mechanical properties with a Young's modulus of 21 GPa and an ultimate strength of 320 MPa. Moreover, hemicellulose imparts recyclability from the dried state. Altogether, this native CNF represents a class of colloidally stable, eco-friendly, low-cost CNF of small diameter for large-scale applications of nanopaper and nanomaterials., QC 20200226

Cellulosic paper products based on sustainable resources are of interest as a replacement for petroleum-based plastics, for example, in packaging applications. Improvements are desired for mechanical performance, recyclability, and possibilities to shape fiber networks into complex geometries. Commercial bleached wood fibers from the kraft process have insufficient mechanical properties for many applications, even with beating and additives. In addition, mechanical properties of paper structures are significantly reduced after recycling. Here, recycling and 3D shaping performance of holocellulose fibers are compared with kraft fibers and investigated in the context of wood fiber tailoring for eco-friendly materials. Holocellulose fibers from wood are prepared by mild peracetic acid delignification for well-preserved nanostructures and hemicellulose content (28 wt %). Paper structures of about 50% porosity are prepared from both types of fibers by vacuum filtration and drying. Mechanical tensile tests are performed, and fracture surfaces are investigated. The effects of recycling on the fiber structure (chemical composition, morphology, and crystallite size in fibers) and mechanical paper properties are reported. 3D-shaping performance is studied using compression molding with a double-curved mold. Holocellulose paper structures showed much better mechanical properties than kraft fiber paper (Young's modulus 10 GPa, ultimate tensile strength 100 MPa), as well as better recycling performance (only 26% decrease in strength after 5 cycles) and 3D formability. The well-preserved cellulose and hemicellulose components are important, as well as the homogeneity of the fiber cell wall nanostructure. This preserves the intrinsic mechanical properties of fibers, reduces hornification effects, and provides strong interfiber adhesion. Furthermore, the water-soluble hemicelluloses present at the cellulose-cellulose interface are able to facilitate recycling and 3D forming., QC 20200217