Characteristics of bamboo tissue in relation to cooling set

To clarify the effects of tissue and structure of bamboo on its bending properties and set by cooling (bent at 90°C and cooled to 20°C with bending), the effects of set in bast-fiber-rich (B_fib) and parenchyma-cell-rich (B_par) specimens were investigated with regard to their dynamic viscoelastic properties, chemical composition, and recovery from deformation with time. The results are summarized as follows: (1) while no clear effect of the proportion of parenchyma cells and bast fibers on residual set immediately after cooling was found, the relative recovery from the deformation with time for B_fib was larger than that for B_par. (2) Slightly higher lignin content and a-cellulose were seen in B_fib than in B_par. (3) The peak temperature of loss modulus (E″) found for B_par, which was attributable to micro-Brownian motion of lignin, was obviously lower than that for B_fib. This was considered to be due to differences in the degree of condensation of lignin or higher-order structure. From these results, it was deduced that the bastfiber-rich specimen, which showed a higher peak temperature regarding thermal softening of lignin allowing the induction of insufficient thermal-softening in the range of 20° to 90°C, caused a larger recovery from deformation with time. Part of this report was presented at the 56th Annual Meeting of the Japan Wood Research Society in Akita, August 2006     

The effect of lignin on the bending properties and fixation by cooling of wood

To clarify the effects of lignin on the fixation of bending deformation by cooling, cooling set for delignified woods with various lignin residues were investigated to compare with mechanical and dynamic viscoelastic properties. Bending tests showed that steep reductions occurred in the modulus of elasticity and modulus of rupture with delignification during the initial stage of delignification. The dynamic viscoelastic measurements revealed that the peak temperature of tan δ due to micro-Brownian motion of lignin was reduced with delignification, and the peak disappeared in the temperature range of 5°–100°C for the specimens that had lost more than 21% of their weight. On the other hand, no clear change in residual set was found in the range of 0%–15% of weight loss in spite of a marked reduction in lignin content. Subsequently, set decreased steeply for the specimens delignified beyond 15% of weight loss. It was suggested that cooling set is not determined solely by lignin content but is influenced by changes in the quality of lignin due to delignification. Lignin quality affects the balance of the elastic potential to recover from deformation and its viscosity, which is an indication of resistance against flow. Part of this report was presented at the 57th Annual Meeting of the Japan Wood Research Society, Hiroshima, August 2007     

Cooling set and its recovery in water-saturated bamboo under large bending deformation

To clarify the bending properties and cooling set for bamboo under large deformation, the relationship between applied deflection and residual deflection was investigated, and comparison was made with the results of thermal recovery and anatomical changes due to deformation. No clear effect of initial deflection on set measured after a long time was found for wood and bamboo loaded on the epidermis side (Bepi). On the other hand, set for bamboo loaded on the endodermis side (Bendo) increased with deformation level. Recovery from the deformation with time for Bendo was almost complete at around 1000 min after unloading in the three-point bending method. This recovery behavior was not seen for Bepi or wood. It was considered that no failure was caused in the bent specimen, because most of the deformation was completely recovered by reheating to the temperature at which the specimens were deformed before cooling. The recovery from deformation for B_endo loaded by the four-point bending method continued even after 1000 min. From microscopic observations, shearing deformations were seen for Bendo loaded by the three-point bending method. From these results, it can be considered that shearing deformations between the two loaded points effectively contribute to decreased recovery force from deformations for B_endo. Part of this report was presented at the 54th Annual Meeting of the Japan Wood Research Society in Sapporo, August 2004     

Condensation of lignin during heating of wood

Summary The structural change of lignin during heating of wood was investigated quantitatively by a method combining nucleus exchange and nitrobenzene oxidation. Lignin modification during heating was mainly a diphenylmethane type condensation. About 40 and 75% of noncondensed units in protolignins were converted to diphenylmethane type units by heating of dry and wet wood meals up to 220 °C, respectively. On the other hand, during heating of modified lignin (dioxane lignin) various types of modifications in addition to diphenylmethane type condensation occurred. Lignin modification via the diphenylmethane type condensation was proposed as a new route for its utilization.     

Temperature dependences of the dynamic viscoelastic properties of wood and acetylated wood swollen by water or organic liquids

In this study, to summarize the changes of thermal-softening behaviors of wood and acetylated wood due to differences in the kinds of swelling liquids, the following measurements were conducted. Untreated and acetylated wood samples were swollen by various liquids and the temperature dependences of the dynamic viscoelastic properties were measured after the heating and cooling histories were unified among the samples. The results obtained are as follows. Untreated samples swollen by high-polarity liquid had lower peak temperature of tanδ, however acetylated samples had higher peak temperature of tanδ than those of untreated wood. On the other hand, untreated wood samples swollen by low-polarity liquid had higher peak temperature of tanδ, however acetylated samples had lower peak temperature of tanδ than those of untreated wood. The amount of swelling is determined by interaction between wood and liquid due to proton-accepting power and molar volumes of liquid and so on, therefore the peak temperature of tanδ and degree of reduction in dynamic elastic modulus (E´) with increasing temperature were corresponded to the amount of swelling.     

Creep and stress relaxation behavior for natural cellulose crystal of wood cell wall under uniaxial tensile stress in the fiber direction

We investigated the temporal changes in creep and stress relaxation behavior in both microscopic crystalline cellulose and macroscopic strain of wood specimen using Japanese cypress (Chamaecyparis obtusa Endl.) to understand the viscoelastic properties of wood cell walls. Specimens 600 µm in thickness were observed by the X-ray diffraction and submitted to tensile load. The crystal lattice strain of (004) plane and macroscopic strain of specimen were continuously detected during creep and stress relaxation tests. It was found that the creep compliance based on macroscopic strain showed a gradual increase after instantaneous deformation due to loading and then the parts of creep deformation remained as permanent strain after unloading. On the other hand, crystal lattice strain showed a different behavior for macroscopic strain; it kept a constant value after instantaneous deformation due to loading and then increased gradually after a certain period of time. These differences between macroscopic and microscopic levels were never found in the stress relaxation tests in this study. Relaxation modulus at the macroscopic level only showed a decreasing trend throughout the relaxation process. However crystal lattice strain kept a constant value during the macroscopic relaxation process. In addition, the microfibril angle (MFA) of wood cell wall has a role of mechanical behavior at microscopic level; crystal lattice strains were smaller with increasing MFA at both creep and relaxation processes. Creep compliance and stress relaxation modulus at the macroscopic level decreased and increased with increasing MFA, respectively. Our results on the viscoelastic behavior at microscopic level evidenced its dependency on MFA.     

幼竹竹腔施肥对毛竹材性的影响

通过竹腔施肥试验区与对照区毛竹竹材含水率、全干密度、抗弯强度、抗弯弹性模量、顺纹抗剪强度、纤维素、半纤维素、木质素含量等物理、力学、化学性质的分析测定,比较分析了两者竹材材性的变化情况.结果表明,不同浓度施肥处理间有较大差异,而试验与对照之间差异不显著,毛竹增产剂及幼竹竹腔施肥对毛竹竹材材性的影响不大.     

Influence of histories on dynamic viscoelastic properties and dimensions of water-swollen wood

The influences of heating history, cooling method, and cooling set on microstructures and the mechanical properties of water-swollen wood were studied by measuring viscoelastic properties and dimensional changes while elevating temperatures between 20°C and 90°C. Both the viscoelastic properties and dimensional changes of waterswollen wood in the first heating process were quite different from those in the other heating processes. The results revealed that the molecular state of green wood around room temperature was stabilized and could not return to this state if drying or heating was carried out. Cooling methods greatly affected the viscoelastic properties, while they hardly affected dimensional changes when the temperature was elevated. Localized stress in the microstructures of water-swollen wood produced by quenching affected the mechanical properties in the heating process, while external stress less than the proportional limit caused by a cooling set had no effect. This revealed that much greater localized stress linked to the instability of waterswollen wood than the external stress in relation to the cooling set occurred. Part of this report was presented at the 53rd Annual Meeting of the Japan Wood Research Society, Fukuoka, March 2003     

Mechanical properties of wood in an unstable state due to temperature changes,and analysis of the relevant mechanism IV: effect of chemical components on destabilization of wood

In order to investigate the effects of chemical components and matrix structure on the destabilization of quenched wood, we examined the physical and mechanical properties of steam-treated wood, hemicellulose-extracted wood, and delignified wood, which were treated at different levels. For steam-treated and hemicellulose-extracted wood,the relative relaxation modulus of the quenched sample was lower than that of the respective control sample. For delignified wood, the relative relaxation modulus fell with weight loss and reached a minimum value at a certain weight loss, and subsequently increased significantly. The hygroscopicity of all treated samples changed slightly by steaming, whereas increased with removing the component. More-over, the average volumetric swelling per 1% MC at 100% relative humidity (RH) was less than at 75% RH and 93% RH for component-removed wood. It was clear that a void structure existed. As a result, the destabilization evaluated by the fluidity (1 - E _t/E ₀) of steam-treated wood was influenced by the amount of adsorbed water. For component-removed wood, destabilization increased temporarily at lower weight loss because of nonuniform cohesive structure. At high weight loss, destabilization will decreased because capillary-condensed water gathered in the voids and obstructed the motion of adsorbed water. However, the destabilization of all treated wood changed less than that of chemically modified wood.     

Deformation under a repetition of moisturizing and drying of bamboo subjected to a set in bending

The aim of this study was to elucidate the mechanisms of deformation change of bamboo set during bending with repeated moisturizing and drying. Deformation was represented by the set ratio, defined as the camber height normalized by the initial value of the fixed set. Susceptibility to deformation from moisture changes was estimated by the slope of the plot of the set ratio versus the moisture content. The set ratio decreased gradually during the repetition of moisturizing and drying, a property consistent with general wood materials. When the specimens were previously extracted in hot water, the set ratio increased but the slope did not change. On the other hand, a previous thermal treatment at more than 230°C or a set at less than 60°C affected both the set ratio and the slope: The set ratio decreased, and the slope increased. It is known that at 60°C hemicellulose starts to soften and at 230° C thermal degradation occurs. Thus, hemicellulose may play a role in the deformation properties of bamboo set during bending.Part of this report was presented at the 50th annual meeting of the Japan Wood Research Society, April 2000, Kyoto     

Dynamic viscoelastic behavior of wood under drying conditions

In this study heartwood from a Chinese fir [Cunninghamia lanceolata (Lamb.) Hook] plantation was treated using a high-temperature drying (HTD) method at 115°C, a low-temperature drying (LTD) method at 65°C, and freeze vacuum drying (FVD), respectively. The dynamic viscoelastic properties of dried wood specimens were investigated. The measurements were carried out at a temperature range of −120 to 250°C at four different frequencies (1, 2, 5, and 10 Hz) using dynamic mechanical analysis (DMA). We have drawn the following conclusions: 1) the storage modulus E′ and loss modulus E″ are the highest for HTD wood and the lowest for FVD wood; 2) three relaxation processes were detected in HTD and LTD wood, attributed to the micro-Brownian motion of cell wall polymers in the non-crystalline region, the oscillations of the torso of cell wall polymers, and the motions of the methyl groups of cell wall polymers in the non-crystalline region in a decreasing order of temperatures at which they occurred; and 3) in FVD wood, four relaxation processes were observed. A newly added relaxation is attributed to the micro-Brownian motions of lignin molecules. This study suggests that both the HTD and the LTD methods restrict the micro-Brownian motion of lignin molecules somewhat by the cross-linking of chains due to their heating history. __________ Translated from Journal of Beijing Forestry University, 2008, 30(3): 96–100 [译自: 北京林业大学学报]     

Changes of chemical composition and crystalline of compressed Chinese fir wood in heating fixation

The changes in relative crystalline, chemical composition and internal structure of compressed Chinese fir wood after different heating fixations were found strictly related to fixation conditions. The compressed wood powders were fixed either by heating at different temperatures all resulting in a 10% recovery, or by incubating at 180℃ for different periods with subsequent recovery levels. Both X-ray diffraction and infrared absorption of those samples have been measured. Relative crystalline increases at early stage of heating fixation, and then decreased gradually. Hemicellulose and lignin decomposition were induced by the fixation process, especially at 180℃, and lignin was degraded actively. Furthermore, absorbed water was lost after heating, but cellulose did not change markedly. Although different fixation pathways can result in the same recovery level, the major chemical reactions underlying them vary, which is consistent with the difference of fixation mechanisms.     

γ射线辐照处理竹材的动态黏弹性与温度变化的关系

木质材料的动态黏弹性是指在交变的应力、应变作用下发生的滞后现象和力学损耗(徐有明,2006),是影响材料加工利用的重要因素。研究表明:木材在不同的含水率下,或经干燥、压缩等不同处理后,其动态黏弹性均会发生改变(蒋佳荔等,     

三种竹碎料板的物理力学性能比较分析

对三种竹碎料板的物理力学性能进行了比较分析。板材弹性模量：竹席增强竹碎料板〉竹碎料/木纤维复合板〉普通竹碎料板;静曲强度：竹席增强竹碎料板〉竹碎料/木纤维复合板〉普通竹碎料板;吸水率：普通竹碎料板〉竹碎料/木纤维复合板〉竹席增强竹碎料板;吸水厚度膨胀率：普通竹碎料板〉竹碎料/木纤维复合板〉竹席增强竹碎料板;内结合强度：竹碎料/木纤维复合板〉竹席增强竹碎料板〉普通竹碎料板。     

基于弯曲挺度法的缠绕用薄竹篾柔性表征

利用竹材的高柔性制造的竹缠绕复合材料是竹材创新利用的革命性产品。深入研究竹材柔性表征方法、评价指标和内在机理可为定向仿生制备高性能竹缠绕复合材料和优化竹缠绕管道工艺提供理论指导。探索弯曲挺度法表征缠绕用薄竹篾柔性的适用性,比较竹材维管束梯度结构和木材木射线组织微观结构差异对竹、木材柔性的影响机制。结果表明:弯曲挺度法适用于缠绕用薄竹篾的柔性表征,该法可快速、准确地获得不同竹篾薄层的柔度。适宜的测试条件为:跨厚比不小于100,加载角速率为600~1800(°)/min。竹材柔性具有梯度性:从竹黄到竹青,随着纤维比量增加,竹篾(50 mm×5 mm×1 mm)柔度从2.92×10-3 mN-1·m-1降低至1.07×10-3 mN-1·m-1,竹材柔性降低。利用混合定律获得竹材维管束和薄壁细胞的弯曲模量和柔度(厚1 mm)理论值分别为0.365 GPa、28.82 GPa和3.284×10-2 mN-1·m-1、0.42×10-3 mN-1·m-1。在相同含水率、尺寸和密度下,竹、木材比柔度排序为竹黄侧>竹青侧>木材,木材柔性低是横向木射线组织限制其柔性变形所引起的。     

Swelling of acetylated wood II: effects of delignification on solvent adsorption of acetylated wood

To clarify the role of lignin in the affinities of acetylated wood for organic solvents, the effects of delignification on the solvent adsorption of acetylated wood were investigated. Acetylated wood meals rapidly adsorbed organic solvents that were hardly adsorbed by unmodified wood. For nonpolar and low-polarity organic solvents, a clear positive correlation was observed between the amount of adsorption and the lignin content. This indicated that acetylated lignin was responsible for the excellent affinities of acetylated wood for hydrophobic organic solvents. On the other hand, for lower alcohols and water, the amount of adsorption reduced with an increase in the lignin content. It was suggested that the adsorption of such polar solvents was dominated by insufficiently acetylated hydrophilic polysaccharides.     

Effect of moisture content on fatigue behavior in the non-linear region for wood

Summary For oven-dried wood applied non-linear deflection, the temperature rising AT was constant after the initially slight temperature rising, and then arose immediately before fatigue failure. Moreover, there was not the rapid reduction of dynamic stress as observed for moist wood. On the other hand, the process to fatigue failure for various moist wood depended upon the moisture content. For heating vs. moisture content, the heating increased with moisture content up to 13 to 20%, while it decreased gradually above 20%. The processes to fatigue failure at more than 13% moisture content were similar to one another. These results were explained on energy balance between the heating due to flexibility of moist molecules in wood substances and the energy consumption for moisture movement and vaporization. The present results supported the mechanism of fatigue behavior in the non-linear region which was proposed in the previous report.     

Compression behaviors of acetylated wood in organic liquids. Part II. Drying-set and its recovery

Unmodified and acetylated cedar wood specimens were swollen in various liquids and dried under radial compression. Two stress relaxation processes were observed during drying, and the second process observed below the fiber saturation point was responsible for the drying-set and the temporary fixation of compressive deformation. The fixed shape of acetylated wood was partly recovered by soaking it in water and toluene and completely recovered in acetone. The effective shape fixation and recovery of toluene-swollen samples implied that the intermolecular hydrogen bonding was not necessary for the drying-set of acetylated wood. The degree of shape recovery was not explained by initial softening, while the acetylated wood always exhibited greater recoverability than unmodified wood. Although 85% stiffness was lost after large compression set and recovery of unmodified wood, such a stiffness loss was limited to 39% when the acetylated wood was processed with organic liquids. This indicated that the swelling of the hydrophobic region in the acetylated wood was effective in preventing mechanical damage due to large compressive deformation.     

Formation and deposition of pseudo-lignin on liquid-hot-water-treated wood during cooling process

Pseudo-lignin induced by high-severity dilute acid treatment of lignocellulose has been widely studied because of its detrimental effect on enzymatic hydrolysis. However, cooling-induced pseudo-lignin (CIPL) formed during the cooling process after treatment has always been ignored and never been characterized systematically. To investigate the formation and chemistry of CIPL, liquid hot water treatments of poplar wood were conducted. Samples of treated wood and hydrolysate were taken out from digester at various temperatures during the cooling process for characterization. SEM images evidenced a progressive deposition of CIPL on the surface of the treated wood during cooling process with a yield of 19.6 mg/g treated wood. However, the treated wood which was collected isothermally at reaction temperature showed no pseudo-lignin. Variation of organic compounds in hydrolysate from lignocellulose degradation during cooling process revealed that depolymerized lignin and furfural accounted for 80.4 and 10.6 % of CIPL, respectively, while soluble saccharides from carbohydrate hydrolysis were independent from CIPL formation. These findings stress the importance of isothermal separation of treated wood and hydrolysate. Otherwise, CIPL should hinder enzymatic hydrolysis for biofuels production or delignification for cellulosic fiber production.     

Cellular UV-microspectrophotometric investigations on pine wood ( Pinus taeda and Pinus elliottii) delignification during biopulping with Ceriporiopsis subvermispora (Pilát) Gilbn. & Ryv. and alkaline sulfite/anthraquinone tr

Scanning UV-microspectrophotometry was used to investigate the topochemistry of lignin removal from pine wood (Pinus taeda and P. elliottii) chips during biopulping involving wood treatment with Ceriporiopsis subvermispora (Pilát) Gilbn. & Ryv. followed by alkaline sulfite/anthraquinone delignification. A delignification front starting from the lumen towards the compound middle lamella was clearly observed in micrographs recorded from individual cell wall layers of wood samples biotreated for 30 days. Lignin was removed without cell wall erosion. UV-micrographs of wood samples cooked for a short time (90 min pulping) showed that the S2 of biotreated samples are more homogeneously delignified compared to the S2 of the undecayed controls. Similarly, the compound middle lamella and cell corners are also more delignified in biotreated samples. On the other hand, UV-micrographs of samples cooked for a long time (150 min pulping at 170°C) showed that there are no significant differences in the contents of residual lignin retained in the S2 of undecayed and biotreated wood samples.