Formation of xylem tissues and secondary cell walls is diminished by severe and consecutive insect defoliation.

PREMISE: Insect defoliation of trees causes unusual changes to wood anatomy and slows radial growth that decreases tree value; however, the characteristics of these anatomical changes in hardwoods remain unclear. The aim of this study was to characterize the anatomy and histochemistry of the wood in trunks of Betula maximowicziana trees after severe insect defoliation. METHODS: Secondary xylem tissues were sampled from trunks that had been defoliated by Caligula japonica at Naie and Furano in central Hokkaido during 2006-2012, then cross-dated and examined microscopically and stained histochemically to characterize anatomical and chemical changes in the cells. RESULTS: White rings with thin-walled wood fibers and greatly reduced annual ring width in the subsequent year were observed in samples from both sites. From these results, the year that the white rings formed was determined, and severe defoliation was confirmed to trigger white ring formation. The characteristics may prove useful to detect the formation year of white rings. Scanning electron microscopy and histochemical analyses of the white rings indicated that the thickness of the S2 layer in the wall of wood fiber cells decreased, but xylan and lignin were still deposited in the cell walls of wood fibers. However, the walls of the fibers rethickened after the defoliation. CONCLUSIONS: Our results suggest that B. maximowicziana responds to a temporary lack of carbon inputs due to insect defoliation by regulating the thickness of the S2 layer of the cell wall of wood fibers. For B. maximowicziana, insect defoliation late in the growing season has serious deleterious effects on wood formation and radial growth.

N-Doped Carbon Fibers Derived from Porous Wood Fibers Encapsulated in a Zeolitic Imidazolate Framework as an Electrode Material for Supercapacitors.

Developing highly porous and conductive carbon electrodes is crucial for high-performance electrochemical double-layer capacitors. We provide a method for preparing supercapacitor electrode materials using zeolitic imidazolate framework-8 (ZIF-8)-coated wood fibers. The material has high nitrogen (N)-doping content and a specific surface area of 593.52 m2 g-1. When used as a supercapacitor electrode, the composite exhibits a high specific capacitance of 270.74 F g-1, with an excellent capacitance retention rate of 98.4% after 10,000 cycles. The symmetrical supercapacitors (SSCs) with two carbon fiber electrodes (CWFZ2) showed a high power density of 2272.73 W kg-1 (at an energy density of 2.46 W h kg-1) and an energy density of 4.15 Wh kg-1 (at a power density of 113.64 W kg-1). Moreover, the SSCs maintained 81.21% of the initial capacitance after 10,000 cycles at a current density of 10 A g-1, which proves that the SSCs have good cycle stability. The excellent capacitance performance is primarily attributed to the high conductivity and N source provided by the zeolite imidazole framework. Because of this carbon material's unique structural features and N-doping, our obtained CWFZ2 electrode material could be a candidate for high-performance supercapacitor electrode materials.

CoP Nanoparticle Confined in P, N Co-Doped Porous Carbon Anchored on P-Doped Carbonized Wood Fibers with Tailored Electronic Structure for Efficient Urea Electro-Oxidation.

Electronic structure optimization and architecture modulation are widely regarded as rational strategies to enhance the electrocatalysts catalytic performance. Herein, a hybridization of ZIF-67-derived CoP nanoparticles embedded in P, N co-doped carbon matrix (PNC) and anchored on P-doped carbonized wood fibers (PCWF) is constructed using a simple simultaneous phosphorization and carbonization strategy. Benefiting from the optimized surface/interface electronic structures, abundant exposed active sites, and outstanding conductivity, the CoP@PNC/PCWF can drive the urea oxidation reaction (UOR) with greater activity and better stability than most recently reported electrocatalysts, in which a potential as low as 1.32 V (vs reversible hydrogen electrode, RHE) is needed to reach 50 mA cm-2 and shows excellent durability. Furthermore, for overall urea splitting, using the CoP@PNC/PCWF electrocatalyst as the anode and commercial Pt/C supported on nickel foam as the cathode, an ultralow cell voltage of 1.50 V (vs RHE) is expected to achieve the 50 mA cm-2 and operate continuously for more than 50 h at 20 mA cm-2 . The reported strategy may shed light on the use of renewable resources to design and synthesize high-performance non-Ni-based phosphides UOR electrocatalysts for energy-saving H2 production.

Mechanical and Hydrothermal Aging Behaviour of Polyhydroxybutyrate-Co-Valerate (PHBV) Composites Reinforced by Natural Fibres.

Biodegradable composites based on poly (3-hydroxybutyrate-co-3-hydroxyvalerate), reinforced with 7.5% or 15% by weight of wood fibers (WF) or basalt fibers (BF) were fabricated by injection molding. BF reinforced composites showed improvement in all properties, whereas WF composites showed an increase in Young's modulus values, but a drop in strength and impact properties. When compared with the unmodified polymer, composites with 15% by weight of BF showed an increase of 74% in Young's modulus and 41% in impact strength. Furthermore, the experimentally measured values of Young's modulus were compared with values obtained in various theoretical micromechanical models. The Haplin-Kardas model was found to be in near approximation to the experimental data. The morphological aspect of the biocomposites was studied using scanning electron microscopy to obtain the distribution and interfacial adhesion of the fibers. Additionally, biodegradation tests of the biocomposites were performed in saline solution at 40 °C by studying the weight loss and mechanical properties. It was observed that the presence of fibers affects the rate of water absorption and the highest rate was seen for composites with 15% by weight of WF. This is dependent on the nature of the fiber. After both the first and second weeks mechanical properties decreased slightly about 10%.

Development of Raw Materials and Technology for Pulping-A Brief Review.

Paper is one of the most significant inventions in human civilization, which considerably advanced global cultural development. Pulping is a key step in the conversion of fiber raw materials into paper. Since its inception, pulping has rapidly evolved, continually adapting to technological advancements. Researchers are constantly investigating various types of raw materials for pulping. In this review, some of the materials employed in pulping are outlined, and the fiber content, pulping method, as well as the strength of wood and non-wood crop straw as pulping raw materials are analyzed and discussed. In addition, this review explores the effects of different materials under various pulping conditions and assesses the future trends in raw material selection for pulping while considering the current global environmental pressures.

Approaching Self-Bonded Medium Density Fiberboards Made by Mixing Steam Exploded Arundo donax L. and Wood Fibers: A Comparison with pMDI-Bonded Fiberboards on the Primary Properties of the Boards.

This study presents an unexplored method to produce formaldehyde-free MDF. Steam exploded Arundo donax L. (STEX-AD) and untreated wood fibers (WF) were mixed at different mixing rates (0/100, 50/50, and 100/0, respectively) and two series of boards were manufactured, with 4 wt% of pMDI, based on dry fibers, and self-bonded. The mechanical and physical performance of the boards was analyzed as a function of the adhesive content and the density. The mechanical performance and dimensional stability were determined by following European standards. The material formulation and the density of the boards had a significant effect on both mechanical and physical properties. The boards made solely of STEX-AD were comparable to those made with pMDI, while the panels made of WF without adhesive were those that performed the worst. The STEX-AD showed the ability to reduce the TS for both pMDI-bonded and self-bonded boards, although leading to a high WA and a higher short-term absorption for the latter. The results presented show the feasibility of using STEX-AD in the manufacturing of self-bonded MDF and the improvement of dimensional stability. Nonetheless, further studies are needed especially to address the enhancement of the internal bond (IB).

Mechanical and Thermal Properties of Wood-Fiber-Based All-Cellulose Composites and Cellulose-Polypropylene Biocomposites.

This article explores wood-fiber-based fabrics containing Lyocell yarn in the warp and Spinnova-Lyocell (60%/40%) yarn in the weft, which are used to form unidirectional all-cellulose composites (ACC) through partial dilution in a NaOH-urea solution. The aim is to investigate the role of the yarn orientation in composites, which was conducted by measuring the tensile properties in both the 0° and 90° directions. As a reference, thermoplastic biocomposites were prepared from the same fabrics, with biobased polypropylene (PP) as the matrix. We also compared the mechanical and thermal properties of the ACC and PP biocomposites. The following experiments were carried out: tensile test, TGA, DSC, DMA, water absorption test and SEM. The study found no significant difference in tensile strength regarding the Spinnova-Lyocell orientation between ACC and PP biocomposites, while the composite tensile strength was clearly higher in the warp (Lyocell) direction for both composite variants. Elongation at break doubled in ACC in the Lyocell direction compared with the other samples. Thermal analysis showed that mass reduction started at a lower temperature for ACC, but the thermal stability was higher compared with the PP biocomposites. Maximum thermal degradation temperature was measured as being 352 °C for ACC and 466 °C for neat PP, and the PP biocomposites had two peaks in the same temperature range (340-474 °C) as ACC and neat PP combined. ACCs absorbed 93% of their own dry weight in water in just one hour, whereas the PP biocomposites BC2 and BC4 absorbed only 10% and 6%, respectively. The study highlights the different properties of ACC and PP reference biocomposites that could lead to further development and research of commercial applications for ACC.

Improving the degree of polymerization of cellulose nanofibers by largely preserving native structure of wood fibers.

The degree of polymerization (DP) of cellulose plays an essential role in unlocking the superior mechanical potential of wood cellulose nanofibrils (CNFs). However, severe degradation of cellulose chains during the chemical pulping is a big challenge to obtain CNFs with high DP. In this work, we tend to improve the DP of wood CNFs by significantly preserving the native structure of wood fibers in an industrial method. Wood sticks are first pretreated with hydrothermal treatment to partially remove hemicellulose, thus leading to an increased porous structure that facilitates the penetration of cooking liquid and lignin removal during delignification, and dilute-alkali-sulfate pulping is then employed to obtain wood fibers with highest viscosity average DP (DPV) of nearly 2400. After that, the as-prepared wood fibers with high DP are separated into CNFs with highest average DPV of 1333. Finally, we demonstrate the potential application of wood CNFs with improved DPV in the fabrication of strong and tough isotropic films and macrofibers.

New Composite Materials Made from Rigid/Flexible Polyurethane Foams with Fir Sawdust: Acoustic and Thermal Behavior.

The aim of this work is to obtain new materials with improved sound absorbing and thermal properties, using rigid or flexible polyurethane foam reinforced with recycled fir sawdust from wood processing as well as by optimizing their mixing ratio. In this respect, we prepared and characterized samples by mixing rigid polyurethane foam (RPUF)/flexible polyurethane foam (FPUF) with 0, 35, 40, 45, and 50 wt% fir sawdust (FS) with grains size larger than 2 mm. The samples were evaluated by cell morphology analysis, sound absorption, and thermal insulation performance. The obtained composite materials containing 50% sawdust have superior acoustic properties compared to those with 100% FPUF in the range of 420-1250 Hz. The addition of 35% and 50% FS in the FPUF matrix led to improved thermal insulation properties and decreased thermal insulation properties in the case of RPUF. The results show that the use of FS-based composites with the FPUF/RPUF matrix for sound absorption and thermal insulation applications is a desirable choice and could be applied as an alternative to conventional synthetic fiber-based materials and as a recycling method of waste wood.

The Effect of Alkaline Treatment on Poly(lactic acid)/Date Palm Wood Green Composites for Thermal Insulation.

In this work, the effect of alkaline treatment on the thermal insulation and mechanical properties of date palm wood fibers (DPWF) and polylactic acid (PLA) green composite was studied. Alkaline treatment was applied to DPWF using two different solutions: sodium hydroxide (NaOH) and potassium hydroxide (KOH), with concentration of 2 vol.%. The fibers were later incorporated into PLA with weight percentages from 10 to 40 wt.%, to form three composite types: PLA with untreated fibers (PLA-UTDPWF), PLA with KOH treated fibers (PLA-KOH), and PLA with NaOH treated fibers (PLA-NaOH). The prepared composites were for use as a green thermal insulation material. The composites were tested to assess the effect of treatment on their physical (density and degree of crystallization), thermal (thermal conductivity, specific heat capacity, thermal diffusivity, thermal degradation, glass transition, and melting temperature), and mechanical properties. Moreover, the composite structural characteristics were investigated using FTIR and SEM analysis. The alkaline treatment significantly increased the crystallinity of the composites, specifically for higher filler loadings of 30 and 40 wt.%. The crystallinity for the 40 wt.% increased from 33.2% for PLA-UTDPWF, to 41% and 51%, for PLA-NaOH and PLA-KOH, respectively. Moreover, the alkaline treatment reduced the density and produced lighter composites than the untreated specimens. For instance, the density of 40 wt.% composite was reduced from 1.43, to 1.22 and 1.30 gcm3 for PLA-NaOH and PLA-KOH, respectively.

Comparison of Melting Processes for WPC and the Resulting Differences in Thermal Damage, Emissions and Mechanics.

The necessity for resource-efficient manufacturing technologies requires new developments within the field of plastic processing. Lightweight design using wood fibers as sustainable reinforcement for thermoplastics might be one solution. The processing of wood fibers requires special attention to the applied thermal load. Even at low processing temperatures, the influence of the dwell time, temperature and shear force is critical to ensure the structural integrity of fibers. Therefore, this article compares different compounding rates for polypropylene with wood fibers and highlights their effects on the olfactory, visual and mechanical properties of the injection-molded part. The study compares one-step processing, using an injection-molding compounder (IMC), with two-step processing, using a twin-scew-extruder (TSE), a heating/cooling mixer (HCM) and an internal mixer (IM) with subsequent injection molding. Although the highest fiber length was achieved by using the IMC, the best mechanical properties were achieved by the HCM and IM. The measured oxidation induction time and volatile organic compound content indicate that the lowest amount of thermal damage occurred when using the HCM and IM. The advantage of one-time melting was evened out by the dwell time. The reinforcement of thermoplastics by wood fibers depends more strongly on the structural integrity of the fibers compared to their length and homogeneity.

Thermoplastic Hybrid Composites with Wood Fibers: Bond Strength of Back-Injected Structures.

Due to their lightweight potential and good eco-balance, thermoplastic hybrid composites with natural fiber reinforcement have long been used in the automotive industry. A good alternative to natural fibers is wood fibers, which have similar properties but are also a single-material solution using domestic raw materials. However, there has been hardly any research into wood fibers in thermoplastic back-injected hybrid composites. This article compares the bond strength of an injection molded rib from polypropylene (PP) and wood fibers to different non-wovens. The non-wovens consisted of wood fibers (spruce) or alternatively natural fibers (kenaf, hemp), both with a polypropylene matrix. Pull-off and instrumented puncture impact tests show that, given similar parameters, the natural and wood-fiber-hybrid composites exhibit very similar trends in bond strength. Further tests using viscosity measurements, microscopy, and computed tomography confirm the results. Wood-fiber-reinforced thermoplastic hybrid composites can thus compete with the natural fiber composites in terms of their mechanical behavior and therefore present a good alternative in technical semi-structural applications.

Lightweight Insulation Boards Based on Lignocellulosic Particles Glued with Agents of Natural Origin.

In this study, the possibility of using adhesives of natural origin for the manufacture of wood fiber-based lightweight panels was investigated. The boards, of a density ranging from 150 to 250 kg/m3, were glued together using commercial urea-formaldehyde resin (control board), solutions of rye flour and potato starch and two types of starch: oxidized and gelatinized. The density and density profile, compressive strength, modulus of elasticity, acoustic properties and thermal conductivity were determined in the produced boards. These studies show that when food components are used as binding agents in the manufacture of lightweight wood fiberboards, the properties obtained can be comparable with those of commercial boards manufactured using synthetic agents.

New composite material based on Kaolinite, cement, TiO2 for efficient removal of phenol by photocatalysis.

Photocatalysis is one of the most important process and was used to eliminate various organic pollutants as phenol in water. In this research study, a new composite containing Kaolinite, cement, and wood fibers modified by titanium oxide TiO2 was elaborated in order to be used in addition of building materials, as photocatalyst for the degradation of phenol. Different kinds and amounts of TiO2 (PC500, P90, and C-TiO2) were immobilized by a simple method inside the composite materials based. The matrix of the hybrid materials was characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), N2 adsorption-desorption (BET), and scanning electron microscope (SEM). These investigations confirmed the dispersion of titania in the new composite materials. The FTIR result has shown that clay particles were successfully treated before their insertion in the composite, by the appearance of two peaks at 2921-2851 cm-1. The XRD results reveal the identification of crystalline phase of TiO2 as anatase. The photocatalytic activity of the composite materials was investigated towards degradation of phenol in aqueous solution under UV light irradiation (369 nm). It has been found that photocatalytic efficiency was significantly enhanced when TiO2 is added. The highest photocatalytic activity has been shown by 3% P90-comp of 41.65% in comparison with 3% PC500 and 3% C-TiO2 which are 29.88% and 22.64 %, respectively. It was shown that the experimental data of kinetic reaction are well fitted by first-order model.

Combining Fiber Enzymatic Pretreatments and Coupling Agents to Improve Physical and Mechanical Properties of Hemp Hurd/Wood/Polypropylene Composite.

Natural fiber/plastic composites combine the low density and excellent mechanical properties of the natural fiber with the flexibility and moisture resistance of the plastic to create materials tailored to specific applications in theory. Wood/plastic composites (WPC) are the most common products, but many other fibers are being explored for this purpose. Among the more common is hemp hurd. Natural fibers are hydrophilic materials and plastics are hydrophobic, therefore one problem with all of these products is the limited ability of the fiber to interact with the plastic to create a true composite. Thus, compatibilizers are often added to enhance interactions, but fiber pretreatments may also help improve compatibility. The effects of pectinase or cellulase pretreatment of wood/hemp fiber mixtures in combination with coupling agents were evaluated in polypropylene panels. Pretreatments with pectinase or cellulase were associated with reduced thickness swell (TS24h) as well as increased modulus of rupture and modulus of elasticity. Incorporation of 5.0% silane or 2.5% silane/2.5% titanate as a coupling agent further improved pectinase-treated panel properties, but was associated with diminished properties in cellulase treated fibers. Combinations of enzymatic pretreatment and coupling agents enhanced fiber/plastic interactions and improved flexural properties, but the effects varied with the enzyme or coupling agent employed. The results illustrate the potential for enhancing fiber/plastic interactions to produce improved composites.

Insight into the Surface Properties of Wood Fiber-Polymer Composites.

The surface properties of wood fiber (WF) filled polymer composites depend on the filler loading and are closely related to the distribution and orientation in the polymer matrix. In this study, wood fibers (WF) were incorporated into thermoplastic composites based on non-recycled polypropylene (PP) and recycled (R-PP) composites by melt compounding and injection moulding. ATR-FTIR (attenuated total reflection Fourier transform infrared spectroscopy) measurements clearly showed the propagation of WF functional groups at the surface layer of WF-PP/WF-R-PP composites preferentially with WF loading up to 30%. Optical microscopy and nanoindentation method confirmed the alignment of thinner skin layer of WF-PP/WF-R-PP composites with increasing WF addition. The thickness of the skin layer was mainly influenced by the WF loading. The effect of the addition of WF on modulus and hardness, at least at 30 and 40 wt.%, varies for PP and R-PP matrix. On the other hand, surface zeta potential measurements show increased hydrophilicity with increasing amounts of WF. Moreover, WF in PP/R-PP matrix is also responsible for the antioxidant properties of these composites as measured by DPPH (2,2'-diphenyl-1-picrylhydrazyl) assay.

Sustainable Development of Hot-Pressed All-Lignocellulose Composites-Comparing Wood Fibers and Nanofibers.

Low-porosity materials based on hot-pressed wood fibers or nanocellulose fibrils (no polymer matrix) represent a new concept for eco-friendly materials with interesting mechanical properties. For the replacement of fossil-based materials, physical properties of wood fiber materials need to be improved. In addition, the carbon footprint and cumulative energy required to produce the material also needs to be reduced compared with fossil-based composites, e.g., glass fiber composites. Lignin-containing fibers and nanofibers are of high yield and special interest for development of more sustainable materials technologies. The present mini-review provides a short analysis of the potential. Different extraction routes of lignin-containing wood fibers are discussed, different processing methods, and the properties of resulting fiber materials. Comparisons are made with analogous lignin-containing nanofiber materials, where mechanical properties and eco-indicators are emphasized. Higher lignin content may promote eco-friendly attributes and improve interfiber or interfibril bonding in fiber materials, for improved mechanical performance.

Wood-Derived Carbon Fibers Embedded with SnO x Nanoparticles as Anode Material for Lithium-Ion Batteries.

Carbon-SnO x composites are obtained by impregnating acetylacetone-treated, delignified wood fibers with tin precursor and successively carbonizing at 1000 °C in 95% argon and 5% oxygen. Scanning electron microscopy and nitrogen sorption studies (Brunauer-Emmett-Teller) show that acetylacetone treatment stabilizes the wood fiber structure during carbonization at 1000 °C and preserves the porous structural features. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy studies show that the small amount of oxygen introduced in inert atmosphere passivates the surface of tin nanoparticles. The passivation process yields thermally and electrochemically stable SnO x particles embedded in carbon matrix. The resultant carbon-SnO x material with 16 wt% SnO x shows excellent electrochemical performance of rate capability from 0.1 to 10 A g-1 and cycling stability for 1000 cycles with Li-ion storage capacity of 280 mAh g-1 at a current density of 10 A g-1. The remarkable electrochemical performance of wood-derived carbon-SnO x composite is attributed to the reproduction of structural featured wood fibers to nanoscale in carbon-SnO x composite and controlled passivation of tin nanoparticles to yield SnO x nanoparticles.

Acoustic Emission-Based Study to Characterize the Crack Initiation Point of Wood Fiber/HDPE Composites.

The crack initiation point can be regarded as a sign of composite failure and plays a vital role in the evaluation of fracture toughness. Wood-plastic composites (WPCs) are viscoelastic materials and the evaluation of fracture mechanism and toughness has a great significance in their applications. Therefore, we used the acoustic emission (AE) technique to measure the crack initiation point of the WPCs and evaluate their fracture toughness. The results show that the novel AE-based methods were more effective than the conventional standard methods for characterization of the crack initiation point. Using the relationship of cumulative AE events with time and load, the critical failure load was quickly determined, and then the critical stress intensity factor and fracture toughness were calculated. The fracture toughness of the WPCs increased with an increase in the wood fiber content.

Compression Strength Mechanisms of Low-Density Fibrous Materials.

In this work we challenge some earlier theoretical ideas on the strength of lightweight fiber materials by analyzing an extensive set of foam-formed fiber networks. The experimental samples included various different material densities and different types of natural and regenerated cellulose fibers. Characterization of the samples was performed by macroscopic mechanical testing, supported by simultaneous high-speed imaging of local deformations inside a fiber network. The imaging showed extremely heterogeneous deformation behavior inside a sample, with both rapidly proceeding deformation fronts and comparatively still regions. Moreover, image correlation analysis revealed frequent local fiber dislocations throughout the compression cycle, not only for low or moderate compressive strains. A new buckling theory including a statistical distribution of free-span lengths is proposed and tested against the experimental data. The theory predicts universal ratios between stresses at different compression levels for low-density random fiber networks. The mean ratio of stresses at 50% and 10% compression levels measured over 57 different trial points, 5.42 ± 0.43, agrees very well with the theoretical value of 5.374. Moreover, the model predicts well the effect of material density, and can be used in developing the properties of lightweight materials in novel applications.