Wood Cell Walls Research Articles

Lightweight, Strong, Hydrostable, Bendable, Rolled‐Up, and Biodegradable Straws Enabled by Nano‐ and Microarchitecture Tuning of the Wood Cell Wall and Molecular Welding Strategy

AbstractPlastic pollution has become a global environmental challenge. Specifically, plastic straws are widely discarded and do not naturally decompose. Paper straws, as alternatives, suffer from weak mechanical strength, poor water/beverage stability, and lack of bendability. Here, an all‐natural plastic substitute is fabricated using a top‐down approach. After lignin is selectively removed from a natural wood slice, the delignified wood is infiltrated with chitosan solution. The chitosan‐infiltrated wood, in its wet state, is highly flexible, moldable, and can be rolled into desired shapes. After drying, strong hydrogen bonds form at the cellulose/chitosan interfaces, making it an all‐natural plastic substitute. By enclosing two sides using a chitosan adhesive, an all‐natural straw is produced with a superior mechanical strength of 242 MPa, higher than polypropylene and paper straws. After baking, the all‐natural straws show high water stability and maintain high mechanical strength in water (136 MPa) and carbonated beverages (71 MPa) for >2 days. A water‐moldable process also creates accordion‐like joints, giving the all‐natural straws superior bendability (120°) and compressibility (50%). The all‐natural straws exhibit high biocompatibility, full biodegradability in 5 months, and high circularity. Overall, the eco‐friendly fabrication of all‐natural straws holds great potential in addressing the ongoing pollution of plastic straws.

Positrons as microprobes to study water-dependent free volume of wood cell walls: a preliminary study

Abstract Positron annihilation lifetime spectroscopy (PALS) was employed to study the water-dependent free volume characteristics of wood cell walls in earlywood and latewood of loblolly pine (Pinus taeda). Measurements were conducted across relative humidity levels (1–80% RH) at room temperature, demonstrating good reproducibility and consistency with polymer science principles. The Tao-Eldrup model was applied to the measured ortho-positronium lifetimes to estimate the mean sizes of free volume elements in wood cell walls. At low relative humidity (below ~ 11%), water absorption resulted in antiplasticization, evidenced by a decrease in mean free volume element sizes. As relative humidity increased, water started acting as a plasticizer, causing the free volume elements to expand. While dry cell walls showed no significant differences in free volume element sizes between earlywood and latewood, earlywood exhibited larger mean free volume element sizes at all higher relative humidity levels. At higher relative humidity levels (above ~ 70% RH), the ortho-positronium lifetimes of cell wall free volume elements overlapped with those of liquid water, indicating PALS cannot provide reliable free volume information at higher cell wall moisture contents. Interpreting the intensity of ortho-positronium annihilation was complicated by the possibility of water inhibiting ortho-positronium formation in wood cell walls.

Hygromechanical deformation of wood cell walls regulated by the microfibril angle

Microfibril angle regulates wood cell wall deformation by influencing moisture diffusion, while hydrogen bonding competition between CNFs and hemicellulose directs water movement.

Lignin hygroexpansion in compression and opposite wood - a molecular dynamics study

Softwood branches develop compression wood (CW) in the lower parts of the branch, while opposite wood (OW) develops on the upper. These wood types differ in structure at several length scales, among others in the chemical composition of their lignin matrix. While OW mostly contains guaiacyl (G) units, CW is known to contain a substantial fraction of 4-hydroxyphenyl (H) lignin. In this study, the impact this difference has on lignin hygroexpansion and interaction with water is studied by the means of atomistic models and molecular dynamics computer simulations of lignin systems at different levels of hydration. It was found that, despite the minor difference in chemical composition, there are differences in swelling, structure and water dynamics. CW lignin is found to have a higher uniaxial swelling coefficient, since the phase separation between lignin and water is more pronounced. This behavior is linked to structural differences, where intermolecular π-π stacking is more common in CW lignin and hydrogen bonding to water more pronounced in OW lignin. These findings are of interest for understanding the role of lignin in CW, and general understanding of moisture interaction with lignin inside wood cell walls.

Detecting Early Degradation of Wood Ultrastructure with Nonlinear Optical Imaging and Fluorescence Lifetime Analysis.

Understanding the deterioration processes in wooden artefacts is essential for accurately assessing their conservation status and developing effective preservation strategies. Advanced imaging techniques are currently being explored to study the impact of chemical changes on the structural and mechanical properties of wood. Nonlinear optical modalities, including second harmonic generation (SHG) and two-photon excited fluorescence (TPEF), combined with fluorescence lifetime imaging microscopy (FLIM), offer a promising non-destructive diagnostic method for evaluating lignocellulose-based materials. In this study, we employed a nonlinear multimodal approach to examine the effects of artificially induced delignification on samples of Norway spruce (Picea abies) and European beech (Fagus sylvatica) subjected to increasing treatment durations. The integration of SHG/TPEF imaging and multi-component fluorescence lifetime analysis enabled the detection of localized variations in nonlinear signals and τ-phase of key biopolymers within wood cell walls. This methodology provides a powerful tool for early detection of wood deterioration, facilitating proactive conservation efforts of wooden artefacts.

Green Nanotechnology of Cell Wall Swelling for Nanostructured Transparent Wood of High Optical Performance.

Transparent wood composites provide new functionalities through active additives distributed at the nanoscale. Scalable nanotechnology includes processing where nanoparticles and molecules are brought into the dense wood cell wall. A novel cell wall swelling step through green chemistry is therefore investigated. Sub-zero centigrade NaOH treatment provides extensive cell wall swelling. Cell wall accessibility is vastly increased so that chemicals can readily impregnate the nanostructured cell wall. Transparent wood with a thickness of up to 15mm can therefore be fabricated. The optical transmittance and the attenuation coefficient are improved since the polymer is distributed inside the cell wall as a matrix for the nanoscale cellulose fibrils. The proposed technology paves the way for scalable wood nanoengineering.

Degradation of logs installed underground for a half century and the microbial communities involved

The use of wood in civil engineering projects is attractive from the perspective of utilizing renewable materials and reducing CO2 emissions. Furthermore, civil engineering presents an appealing opportunity to expand the demand for wood. Wood degradation rates are low in anaerobic environments, such as underground conditions. In this study, the degradation of wood after 55 years in an underground environment was examined by analyzing logs that had been driven underground for a soil stabilization project. Log density was measured and wood cell walls were observed under a microscope to estimate the degree of degradation, and the bacterial and fungal communities living in the sapwood of the logs were examined using a metagenomic approach. The results showed that the wood density was hardly reduced, and that anaerobic cellulolytic bacteria were dominant in the microbial communities in the wood. The degree of wood degradation over 55 years was low, indicating that these logs retained their ground improvement function for at least half a century.

Interconnecting EDOT-Based Polymers with Native Lignin toward Enhanced Charge Storage in Conductive Wood.

The 3D micro- and nanostructure of wood has extensively been employed as a template for cost-effective and renewable electronic technologies. However, other electroactive components, in particular native lignin, have been overlooked due to the absence of an approach that allows access of the lignin through the cell wall. In this study, we introduce an approach that focuses on establishing conjugated-polymer-based electrical connections at various length scales within the wood structure, aiming to leverage the charge storage capacity of native lignin in wood-based energy storage electrodes. We demonstrate that poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) PEDOT/PSS, integrated within the cell wall lumen, can be interfaced with native lignin through the wood cell wall through in situ polymerization of a water-soluble S-EDOT monomer. This approach increases the capacitance of the conductive wood to 315 mF cm-2 at a scan rate of 5 mV s-1, which is seven and, respectively, two times higher compared to the capacitance of conductive wood made with the single components PEDOT/PSS or S-PEDOT. Moreover, we show that the capacitance is contributed by both the electroactive polymers and native lignin, with native lignin accounting for over 70% of the total charge storage capacity. We show that accessing native lignin through in situ creation of electrical interconnections within the wood structure offers a pathway toward sustainable, wood-based electrodes with improved charge-storage capacity for applications in electronics and energy storage.

Fabrication of highly stable and durable wood materials by modification of polyacrylamide (PAM)-glyoxal (GLY)

Facile and efficient protection strategies to improve wood dimensional stability and resistance to mold and termite are urgently needed in the architectural constructional materials market. In this study, polyacrylamide (PAM)-glyoxal (GLY) system impregnation and thermal curing were used to modify Scots pine wood. The results showed that the average anti-swelling efficacy (ASE) of 160-AGE, 160-AGEP, and 200-AGE modified wood was 36.09 %, 26.67 % and 19.00 % in volume, respectively. Compared with the untreated wood, the modified wood exhibited better mold resistance. Furthermore, the modified wood samples show higher termite mortality and lower mass losses, indicating good termite resistance. Among them, the anti-mold efficacy in 200-AGE was 91.10 %, and the termite resistance rating in 160-AGE was 9.2. The modulus of elasticity (MOE) of the modified wood sample was 16–25 % higher than that of the untreated wood. Obtained by infrared spectrum and electron microscope analysis, the acrylamide polymer penetrates into the wood cell cavities and forms polyacrylamide, which is crosslinked to wood cell wall -OH by glyoxal. This study can prove that the polyacrylamide-glyoxal system modifier has great potential as a modifier to improve the mold resistance and dimensional stability of wood.

Dynamic changes of heterogeneous cell wall macromolecules in differentiating conifer xylem using cytochemical localization

Tracing dynamic changes of heterogeneous cell wall components during xylem differentiation is essential for understanding the intricate architecture of wood cell walls at the individual secondary cell wall layer level. Here we employ histochemical- and immunological approaches to visualize the deposition of cellular polymers during xylem differentiation in Pinus bungeana. In axial tracheids, deposition of crystalline cellulose and glucomannan preceded xylan and lignin. Lignification was initiated in primary cell wall corners during development of the S1 layer and intensified with cell wall thickening. Immunofluorescence labeling showed an earlier deposition of glucomannan than xylan with strong presence in S1 layer corner regions at early stages of differentiation. Quantification of immunogold-labeled xylan and glucomannan showed distinct increasing trends during thickening of tracheid wall layers with xylan labeling of the S1 and S2 layers at the S3 stage greater than the S2 stage. Differential cell wall polymer deposition was evident in mature tracheid areas with glucomannan absent in warty layers. Pectins were highly concentrated in unlignified primary cell walls but decreased with axial tracheid wall differentiation. The sequence of polymer deposition in ray cells was similar but lagged behind axial tracheids with ray parenchyma remaining unlignified with thinner cell walls than ray tracheids.

Cellulose consolidated with polyethylene glycol: The nanoscale mechanisms revealed by hybrid Monte Carlo/molecular dynamics modeling

Polyethylene glycol (PEG) consolidation treatment is a widely used conservation strategy for wooden culture relics. However, the consolidation mechanism of PEG is still open to interpretation. PEG-cellulose, the representative component of wood cell wall, interactions are governed by various coupled multi-scale mechanisms which require nano-scale investigation. In this study, a hybrid molecular dynamics and grand canonical Monte Carlo (MD/GCMC) simulation combined with rule of mixture (RoM) analyses are employed to reveal the underlying mechanisms of PEG-induced consolidation. We found that PEG200 reduces moisture adsorption and swelling at museological conditions, confirming its consolidation effect. At high PEG content, a crossover behavior is identified at humid conditions (RH > 80) where excessive sorption and swelling are observed surpassing the untreated sample. The molecular modeling results are found to be consistent with experimental observations. Furthermore, the structural and mechanical properties of the hydrated samples are assessed by examining the porosity distribution, mechanical properties, and hydrogen bonding network. Results indicate mechanical softening induced by PEG treatment. A modified mixture model is proposed based on molecular modeling results that incorporate sorption and swelling coupling, porosity filling and mechanical softening behaviors. Two key mechanisms are identified explaining the consolidation effect of PEG: first, the PEG fills the porosities of amorphous structure thus diminishing sorption sites; second, the polymer structure prohibits PEG from further swelling thus constraining water sorption. The model and theoretical framework can serve as a guide for the design of novel consolidant materials by identifying the key molecular features of an ideal consolidant.

Application risk and value of Cd-enriched poplar wood: Wood properties, leaching characteristics and brown rot resistance

This study investigated the application risk and value of Cd-enriched poplar wood, focusing on its wood properties, leaching characteristics, and brown rot resistance. The results indicated that Cd deposition in cell walls significantly inhibited brown rot fungi, thereby enhancing decay resistance. Furthermore, the extent of improvement in brown rot resistance was linked to wood density: the higher the density of Cd-enriched poplar wood, the stronger its resistance to brown rot. As the Cd concentration increased, the Cd distribution abundance and the wood crystallinity gradually increased. Structural changes were observed, including fluctuating microfibril angle and double wall thickness of fibers and vessels. Cd concentrations exceeding 50 mg/kg altered the chemical composition of the cell walls. The binding form of Cd in wood cell wall showed a trend of bound Cd ＞ free Cd ＞ residual Cd. Cd leaching occurred under cyclic soaking in water, which may lead to secondary contamination. However, under the condition of 75 % relative humidity, Cd leaching was negligible, suggesting potential for safer use in controlled environments. These findings provide valuable insights into the management and application of Cd-enriched wood, especially in contexts where decay resistance is critical or in water-exposed environments.

Combining microscale ATR-FTIR and chemometrics to interpret degradation characteristics of earlywood, latewood, and compression wood in waterlogged archaeological pine wood

Interpreting the degradation characteristics of waterlogged archaeological wood (WAW) is crucial for the conservation of wooden cultural heritage. Generally, multidisciplinary diagnostic methods, including physical, micromorphological, and chemical approaches, are employed to evaluate the preservation state of WAW. However, primarily focused on the sample level, this methodology limits the understanding of the variability in degradation from a detailed perspective. In this paper, we adopted the in-situ microscale attenuated total reflectance Fourier transform infrared (ATR-FTIR) method to investigate the degradation variability in waterlogged archaeological Masson pine (Pinus massoniana) wood excavated from the ancient Chinese shipwreck Nanhai No. 1. Specifically, spectra of earlywood (EW), latewood (LW), and compression wood (CW) were extracted and combined with chemometrics to achieve rapid classification of their degradation levels. The micromorphological features of wood cell walls in conjunction with the ratios of lignin (A1509) and carbohydrate (A1370) peak areas were used to estimate the degradation levels. Unlike recent wood, moderate degradation in CW and severe degradation in EW and LW were classified in archaeological samples. The degradation levels were effectively determined through principal component analysis (PCA) and sparse partial least squares discriminant analysis (sPLSDA). The results suggest that chemometric analysis is a promising method to discern the variable degradation levels of archaeological wood at the tissue level. The methodologies developed in this study provide detailed insights into the degradation characteristics in WAW and improve the accuracy of evaluating the preservation state.

Nanostructured poplar wood via delignification and ammonium dihydrogen phosphate-SiO2 modification towards remarkable flame retardant performance: Synergistic effect and enhanced mechanism

Developing efficient methods to prepare high-performance flame retardant and smoke suppression wood is crucial for the application. Herein, nanostructured poplar wood (DWI-4) with remarkable flame retardant and smoke suppression performance was fabricated by impregnating ammonium dihydrogen phosphate (ADP) and nano-silica (SiO2) into delignified wood (DW-4). With the delignification treatment, lignin was partially removed, and numerous pores and cracks were developed on the cell wall of wood, allowing more ADP-SiO2 particles to be impregnated into wood. As a result, ADP-SiO2 particle was not only anchored in the lumens (pores) of wood, but also was penetrated and embedded into the cell wall, achieving the synergistic modification of the lumen and cell wall of wood. As anticipated, the produced DWI-4 featured outstanding flame retardant and smoke suppression performance. The peak heat release rate (pHRR) of DWI-4 was as low as 38.2 kW m−2, which was only 8 % of that of natural wood (NW). And the total heat release (THR) and total smoke production (TSP) demonstrated reductions of 73.9 % and 64.4 % comparing to NW. Moreover, the compressive strength of DWI-4 increased by 31.4 % comparing to NW. The structure of residual char of DWI-4 was more stable and the gas intensity produced by the combustion of DWI-4 decreased remarkably. Therefore, the synergy of delignification and ADP-SiO2 impregnation significantly enhanced the flame retardant and smoke suppression performance of wood and the enhanced mechanism was revealed. The nanostructured poplar wood with excellent flame retardant and smoke suppression performance was prepared, providing an effective method for the functional improvement of wood and expanding the fields of application.

Role of Lignin in Moisture Interactions of Cellulose Microfibril Structures in Wood

Wood is a complex, multi‐component material with a variety of applications. The properties of wood are especially sensitive to its moisture content and comprehending wood–water interactions is thus paramount. Understanding of the moisture interactions of the wood polysaccharide components, cellulose microfibrils and hemicelluloses, is improving. However, the role of lignin remains less clear. In this work, X‐ray scattering measurements were carried out on delignified spruce undergoing a desorption‐adsorption cycle, and the results were compared to previous data from untreated wood. In addition, a molecular model of the cell wall nanostructure, including the main chemical components, was used to support the experimental results. Based on the small‐angle scattering, delignification affects the arrangement of cellulose microfibrils in the cell wall by increasing their packing distance. Wide‐angle scattering shows that delignification has no substantial effect on the cellulose crystal structure and how it changes with moisture. Both the scattering results and simulations suggest that lignin is a passive, rather than an active participant in the moisture response of microfibril bundles in wood cell walls. Small‐angle scattering from fully wet delignified wood reveals a contribution that can be assigned to aligned nanometer scale pores which close during drying.

A Review on the Effect of Wood Surface Modification on Paint Film Adhesion Properties

Wood surface treatment aims to improve or reduce the surface activity of wood by physical treatment, chemical treatment, biological activation treatment or other methods to achieve the purpose of surface modification. After wood surface modification, the paint film adhesion performance, gluing performance, surface wettability, surface free energy and surface visual properties would be affected. This article aims to explore the effects of different modification methods on the adhesion of wood coating films. Modification of the wood surface significantly improves the adhesion properties of the paint film, thereby extending the service life of the coating. Research showed that physical external force modification improved the hydrophilicity and wettability of wood by changing its surface structure and texture, thus enhancing the adhesion of the coating. Additionally, high-temperature heat treatment modification reduced the risk of coating cracking and peeling by eliminating stress and moisture within the wood. Chemical impregnation modification utilized the different properties of organic and inorganic substances to improve the stability and durability of wood. Organic impregnation effectively filled the wood cell wall and increased its density, while inorganic impregnation enhanced the adhesion of the coating by forming stable chemical bonds. Composite modification methods combined the advantages of the above technologies and significantly improved the comprehensive properties of wood through multiple modification treatments, showing superior adhesion and durability. Comprehensive analysis indicated that selecting the appropriate modification method was key for different wood types and application environments.

Wood Cell Wall Nanoengineering toward Anisotropic, Strong, and Flexible Cellulosic Hydrogel Sensors.

Achieving highly ionic conductive hydrogels from natural wood remains challenging owing to their insufficient surface area and low number of active sites on the cell wall. This study proposes a viable strategy to design a strong and anisotropic wood-based hydrogel through cell wall nanoengineering. By manipulating the microstructure of the wood cell wall, a flexible cellulosic hydrogel is achieved through Schiff base bonding via the polyacrylamide and cellulose molecular chains. This results in excellent flexibility and mechanical properties of the wood hydrogel with tensile strengths of 22.3 and 6.1 MPa in the longitudinal and transverse directions, respectively. Moreover, confining aqueous salt electrolytes within the porous structure gives anisotropic ionic conductivities (19.5 and 6.02 S/m in the longitudinal and transverse directions, respectively). The wood-based hydrogel sensor has a favorable sensitivity and a stable working performance at a low temperature of -25 °C in monitoring human motions, thereby demonstrating great potential applications in wearable sensor devices.

EFFECT OF PHENOL FORMALDEHYDE RESIN IMPREGNATION ON NANODYNAMIC VISCOELASTICITY OF PINUS MASSONIANA LAMB IN WET STATE

We evaluated the effects of phenol formaldehyde (PF) resin modification on Masson pine (Pinus massoniana Lamb.) wood cell wall in wet states. The penetration degree of PF resin into wood cell was determined using confocal laser scanning microscopy (CLSM). The micromechanical properties of PF-modified wood cell walls in wet state were analyzed by quasi-static nanoindentation and dynamic modulus mapping techniques. Results showed that the PF resin significantly affected the static viscoelasticity and nanodynamic viscoelasticity of wood cell walls in oven-dried and wet states. The cell-wall mechanics increased at a PF resin concentration due to the increased bulking effects, such as decreased crystallinity of cellulose. Furthermore, the microfibrillar angle (MFA) of cell walls was lower than that of the control wood cell wall. The cell-wall mechanics of PF resin-modified sample decreased small than control sample in wet states.

Identification of a Fomitopsis pinicola from Xiaoxing’an Mountains and Optimization of Cellulase Activity

Brown-rot fungi are large fungi that can decompose the cell walls of wood; they are notable for their secretion of diverse and complex enzymes that synergistically hydrolyze natural wood cellulose molecules. Fomitopsis pinicola (F. pinicola) is a brown-rot fungus of interest for its ability to break down the cellulose in wood efficiently. In this study, through a combination of rDNA-ITS analysis and morphological observation, the wood decay pathogen infecting Korean pine (Pinus koraiensis Siebold and Zucc.) was identified. Endoglucanase (CMCase) and β-glucosidase were quantified using the DNS (3,5-Dinitrosalicylic acid) method, and the cellulase activity was optimized using a single-factor method and orthogonal test. The results revealed that the wood-decaying fungus NE1 identified was Fomitopsis pinicola with the ITS accession number OQ880566.1. The highest cellulase activity of the strain reached 116.94 U/mL under the condition of an initial pH of 6.0, lactose 15 g·L−1, KH2PO4 0.5 g·L−1, NH4NO3 15 g·L−1, MgSO4 0.5 g·L−1, VB1 0.4 g·L−1, inoculated two 5 mm fungal cakes in 80 mL medium volume cultured 28 °C for 5 days. This laid a foundation for improving the degradation rate of cellulose and biotransformation research, as well as exploring the degradation of cellulose by brown rot fungi.

Production and technical performance of scrimber composite manufactured from industrial low-value wood for structural applications

Development of scrimber composites and other engineered wood products from low-value wood and wood waste provides an effective opportunity to preserve natural resources, minimize waste, and innovate the production of higher-performance, environment-friendly construction materials. In this study, peeler cores, which are the center of poplar logs remaining after the peeling process in the veneer production, were utilized to develop scrimber composites. This study investigated the effects of different resins, including phenol-formaldehyde (PF) and urea formaldehyde (UF), as well as hydrothermal treatments at various temperatures (60 °C and 130 °C), on the physical and mechanical properties of the scrimber composites. Chemical changes in wood components and morphological changes in wood cell walls resulting from hydrothermal treatment were analyzed using Fourier transform infrared spectroscopy and scanning electron microscopy. To clarify how resin type and hydrothermal treatment affect structural performance, several physical and mechanical properties of scrimber composites, including thickness swelling, water absorption, internal bond strength, bending modulus of elasticity, and modulus of rupture, were measured. The test results revealed that hydrothermally treated wood scrims at 130 °C, when bonded with PF resin, produced scrimber composites with superior structural performance.