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1.
We attempted to measure in situ the tensile elastic moduli of individual component polymers with a three-dimensional (3D) assembly mode in the cell walls of Sugi (Cryptomeria japonica D. Don) without isolating the polymers. To prepare wood tangential slices [50 × 6 × 0.2 mm (L × T × R)] consisting of lignin with a 3D assembly mode in the cell walls, cellulose and hemicellulose were removed using the method of Terashima and Yoshida (2006) to obtain methylated periodate lignin slices. To prepare wood slices consisting of polysaccharide with a 3D assembly mode in the cell walls, lignin was removed using the method of Maekawa and Koshijima (1983) to obtain holocellulose slices. Static tensile test was applied to determine the elastic moduli of 3D lignin and 3D polysaccharide slices. The followings were revealed. The elastic modulus of the 3D lignin slices was 2.8 GPa, regardless of the microfibril angle (MFA) in the slices. The elastic moduli of the 3D polysaccharide slices with MFAs of 14°, 23°, 34°, and 42° were 18, 12, 9, and 4 GPa, respectively. The former shows that the lignin with a 3D assembly mode behaves as an isotropic substance in the cell walls, while the latter suggests that the 3D polysaccharide slice shows marked anisotropic structure in the cell wall. Despite the fact that cellulose content increased after lignin removal, values of substantial elastic modulus of the cell wall slightly decreased regardless of MFA. Following two possible reasons were pointed out for explaining this phenomenon. First, lignin removal caused an artifactual deterioration in the polysaccharide slices at the level of macromolecular aggregate. Second, rigid and fusiform-shaped cellulose crystallites are dispersed in the soft matrix of amorphous polysaccharide, and those are loosely connected to each other by the intermediary of matrix polysaccharide. Those suggest that the rigid cellulose crystallite can optimize its strong mechanical performance in the polysaccharide framework of the wood cell wall in combination with the ligninification.  相似文献   

2.
In order to enlarge the utilization field of wood and decrease the costs of carbon fibers, carbon fiber precursors from liquefied wood were prepared by soaking liquefied wood in a solution containing hydrochloric acid and formaldehyde, after melt-spinning by adding hexamethylenetetramine. The microstructure evolution of the precursor during carbonization was studied by FTIR, X-ray analysis and Raman spectroscopy. The results show that precursors from liquefied wood above 400°C had diffraction peaks corresponding to the (100) crystal plane. When the carbonization temperature reached 500°C, Raman spectroscopy showed the D peak at wave number of 1360 cm–1 and the G peak at 1595 cm–1. By increasing the carbonization temperature, the microstructure of the precursors became more ordered. Although the structure of the precursor changed at 500 and 800°C, the peaks at 1632 and 1454 cm–1 corresponding to the characteristic vibrations of aromatic rings, remained during carbonization. This implies that the precursor from liquefied wood cannot be easily formed into graphite.  相似文献   

3.
The carbonization process causes different physical and chemical transformations to wood, affecting the final properties of the charcoal produced. In Brazil, the cutting and use of Ocotea porosa (Nees & Mart. Ex Nees) L. Barroso is legally prohibited. But the difficulty of identifying the species used to produce charcoal hinders enforcement efforts to protect this and other endangered tree species. The aim of this work was to characterize the anatomy of charcoal made from O. porosa at different temperatures to provide information to facilitate differentiation of the species by the authorities in charge of suppressing illegal commerce. Samples were carbonized by direct heating and final temperatures of 350, 450 and 650 °C, besides a group under a ramp heating regime also with a final temperature of 450 °C. The qualitative characteristics of the O. porosa wood were preserved at the carbonization temperatures studied permitting the use of its anatomical structures for identification of carbonized wood to support control of the illegal trade in charcoal of this species.  相似文献   

4.
Pulverized samples of wood, cedar and eucalyptus were treated with 5 N NaOH solutions at 25–150 °C. Hemicellulose and lignin content in the samples decreased with increasing treatment temperatures, while the recovery of glucose was maintained at nearly 90 %. X-ray diffraction analysis showed that the content of the original cellulose I structure in the samples decreased with increasing temperature, and most of the cellulose in the sample treated at 150 °C was converted to cellulose II by mercerization. Enzymatic hydrolysis of the alkaline-treated samples was carried out at 37 °C using solutions comprising a mixture of cellulase and β-glucosidase. The samples treated at higher temperatures showed better enzymatic degradability. Treatment with an alkaline solution of lower concentration (1 N NaOH) at 150 °C was also used. Despite significant quantities of hemicellulose and lignin being removed, mercerization was not induced. The enzymatic degradability was much lower than that of the sample treated with a 5 N NaOH solution at 150 °C. Thus, treatment with concentrated alkaline solution at high temperature led to not only the removal of hemicellulose and lignin, but also to modification of the cellulose structure, which resulted in high efficiency of enzymatic saccharification of the wood samples.  相似文献   

5.
This article presents an experimental study into thermal softening and thermal recovery of the compression strength properties of structural balsa wood (Ochroma pyramidale). Balsa is a core material used in sandwich composite structures for applications where fire is an ever-present risk, such as ships and buildings. This article investigates the thermal softening response of balsa with increasing temperature, and the thermal recovery behavior when softened balsa is cooled following heating. Exposure to elevated temperatures was limited to a short time (15 min), representative of a fire or postfire scenario. The compression strength of balsa decreased progressively with increasing temperature from 20° to 250°C. The degradation rates in the strength properties over this temperature range were similar in the axial and radial directions of the balsa grains. Thermogravimetric analysis revealed only small mass losses (<2%) in this temperature range. Environmental scanning electron microscopy showed minor physical changes to the wood grain structure from 190° to 250°C, with holes beginning to form in the cell wall at 250°C. The reduction in compression properties is attributed mostly to thermal viscous softening of the hemicellulose and lignin in the cell walls. Post-heating tests revealed that thermal softening up to 250°C is fully reversible when balsa is cooled to room temperature. When balsa is heated to 250°C or higher, the post-heating strength properties are reduced significantly by decomposition processes of all wood constituents, which irreversibly degrade the wood microstructure. This study revealed that the balsa core in sandwich composite structures must remain below 200°–250°C when exposed to fire to avoid permanent heat damage.  相似文献   

6.
Sandwich compression of wood that can control the density and position of compressed layer(s) in the compressed wood provides a promising pathway for full valorization of low-density plantation wood. This study aims at investigating the effects of preheating temperatures (60–210 °C) on sandwich compression of wood, with respect to density distribution, position and thickness of the compressed layer(s). Poplar (Populus tomentosa) lumbers with moisture content below 10.0% were first soaked in water for 2 h and stored in a sealed plastic bag for 18 h, the surface-wetted lumbers were preheated on hot plates at 60–210 °C and further compressed from 25 to 20 cm under 6.0 MPa at the same temperature on the radial direction. The compressed lumbers were characterized in terms of density distribution, position and thickness of compressed layer(s). It was found that depending on preheating temperatures, sandwich compressed wood with three structural modes, namely, surface compressed wood, internal compressed wood and central compressed wood can be formed. Density of the compressed layer(s) in wood increased gradually as a result of the elevated preheating temperatures. Higher preheating temperatures gave rise to bigger distance between compressed layer(s) and the surface, and preheating temperature elevation from 90 to 120 °C contributed to a maximal distance increase of 2.71 mm. In addition, higher preheating temperatures resulted in bigger thickness of compressed layer(s) over 60–150 °C and temperature elevation from 120 to 150 °C lead to the layers integration from two into one. Further temperature elevation over 150 °C reduced the thickness of the compressed layer in wood. SEM scanning suggested that cell wall bucking rather than cell wall crack occurred in compressed layer(s) and transition layer(s).  相似文献   

7.
Hiba (Thujopsis dolabrata) wood was treated with supercritical carbon dioxide (scCO2) at stepwise temperature increments from 50° to 400°C continuously so that extractives (dichloromethane-soluble and -insoluble phases) and solid residues were obtained. The yield of extractives from hiba wood increased with increasing extraction temperature. The volatile compounds in the dichloromethane-soluble phase from scCO2 extraction at 50°C contained only terpenoids. However, the volatile compounds in the dichloromethane-soluble phase from scCO2 extraction at 300°C not only contained terpenoids but also phenols, furans, hydrocarbons, and organic acids. The yield of β-thujaplicin, which is a useful compound in hiba wood, increased with increasing extraction temperature from 50°C to 300°C; the optimal conditions for extracting β-thujaplicin were 300°C and 19.61 MPa. Further study of degradated compounds from the cellulosic and lignic materials of hiba wood after stepwise high-temperature scCO2 treatment above 300°C may provide clues to its efficient use.  相似文献   

8.
The influence of inorganic matter on the pyrolysis of Japanese cedar (Cryptomeria japonica) wood was studied at a gasification temperature of 800°C with demineralization through acid washing. Some influences on the formation of char, tar, and low molecular weight products coincided with results reported at temperatures lower than the gasification temperature. However, the carbonization behavior of the volatile products and the yield of polysaccharide fraction were not able to be explained as a sum of the pyrolysis of cellulose, hemicellulose, and lignin even after demineralization. These results suggest some interactions between wood constituent polymers other than the influence of inorganic matter.  相似文献   

9.
Two common wood flooring materials, taun (Pometia spp.) and cumaru (Dipteryx odorata), were used as investigated objects and comparison was made between the two wood species for their density, microstructure, microfibril angle (MFA), cellulose crystallinity and the main chemical composition. Results showed that the density of cumaru was 0.941 g·cm?3, significantly larger than that of taun, 0.737 g·cm?3. The biggest difference of two wood species in microstructures was fiber cells. Fiber cells of cumaru had dense cell walls, almost no cell lumens; while fiber cells of taun had relatively thin cell walls, with apparent cell lumens. The thickness of fiber cell wall of cumaru and taun were 6.80 and 2.82 µm, respectively, and the former is about 2.5 times thicker than the latter. Measured data of MFA indicated that the average MFA of cumaru was 11.7°, smaller than that of taun, 13.4°. The relative crystallinity of cumaru and taun were 54.0 and 50.8%, respectively. The two wood species had the similar holocellulose contents, but the lignin content of cumaru was higher than that of taun, especially that the content of extractive of cumaru was as twice as that of taun.  相似文献   

10.
A new approach is proposed for the evaluation of the brittleness of heat-treated Styrax tonkinensis wood. Heat treatment made wood more brittle when wood was heated at a higher temperature or for a longer time. The brittleness increased to four times that of the control when wood was heated at 200°C for 12 h. For treatment at 160°C, the increase in brittleness without any change in weight is thought to be possibly caused by the relocation of lignin molecules. At higher temperatures, loss of amorphous polysaccharides due to degradation is thought to become the main factor affecting brittleness. The crystallites that were newly formed after 2 h of treatment showed brittleness that was different from that of the inherent crystallites remaining after 12 h of heat treatment. This inherent crystalline cellulose possibly plays a role in brittleness. There is also the possibility of using color to predict the brittleness of heat-treated wood.  相似文献   

11.
Bamboo was carbonized at different temperatures ranging from 200℃ to 600℃.The dependence of the change of hemicellulose,cellulose,and lignin on the temperature was investigated by means of elemental analysis and Fourier Transform Infrared (FTIR) spectra of the residual solid products.The results showed:(1)Below 200℃,hemicellulose in bamboo wasdecomposed and a large amount of hydroxyl groups are dislocated from hemicellulose and cellulose,accompanied by the evolution of water to escape.(2)200℃-250℃,cellulose in bamboo was brastically decomposed whereas the net structure of lignin keep stable,with the except of the dislocation of methoxyl groups from lignin.(3)250℃-400℃,the net structure of lignin collapse,up to 400℃,followed by that the more position in aryl groups are substituted.(4)For bamboo carbonization,the aromatization of residual carbon has approximately completed at the temperature as high as 600℃.But the fusion of aromatic rings possibly does not occur.  相似文献   

12.
Summary The thermochemical degradation of cork from Quercus suber L. was studied in the temperature range 150°C–450°C in relation to mass loss, chemical composition and the influence on the cellular structure. The degradation of cork is strongly dependent on temperature and mass losses become significant at 200°C (15% of initial dry weight) and increase rapidly for higher temperatures (27% at 250 °C, 49% at 300 °C, 62% at 350 °C) until ashing at 450 °C. The polysaccharides are the most heat sensitive components: at 200 °C, hemicelluloses disappear and cellulose is degraded to a considerable extent. Suberin is more resistant and degradation starts at approx. 250 °C; 300 °C-treated samples only contain 7% suberin.The cellular structure of cork is also significantly influenced by temperature. Upon heating, cells expand and the cell walls stretch, attaining at 250 °C a maximum cell volume increase corresponding to a factor of approximately 2. Above 300 °C, the structure of cell walls is considerably changed and show profound physical damage; in the later stages of pyrolysis, a cellular structure is no longer observed.We are grateful to Mrs. Joaquina Ferreira for her help with the chemical analysis. The research was financially supported by the Junta Nacional de Investigação Científica e Tecnológica (JNICT) and by the Instituto de Ciência e Tecnologia dos Materiais (ICTM)  相似文献   

13.
Antifungal and antitermitic activities of wood vinegar produced from Vitex pubescens were evaluated. Three kinds of wood vinegar were produced at three different pyrolysis temperatures, i.e. at 350, 400 and 450 °C. A PDA dilution method was employed to assay antifungal activity of the vinegars with a white-rot fungus Trametes versicolor and a brown-rot fungus Fomitopsis palustris. Termiticidal activity and repellent effect were evaluated by a no-choice test and a choice test with Reticulitermes speratus and Coptotermes formosanus. All wood vinegars exhibited antifungal activity against both fungi. Wood vinegar of 450 °C had the higher activity than those of 400 and 350 °C. It was assumed that acid component contributed to the increase in controlling the growth of fungal. The wood vinegar exhibited antitermite activity to both R. speratus and C. formosanus workers in the no-choice experiment. However, it needed relatively high concentration to obtain the perfect mortality. For instance, the wood vinegar of 10 % concentration was needed to achieve 100 % mortality against C. formosanus, whereas for R. speratus only 3 % of wood vinegar was required. In the direct-choice experiment, wood vinegar had a significantly repellent effect to both termites at the lowest treating concentration of 10 %.  相似文献   

14.
This study has focused on solute diffusing into cell walls in solution-impregnated wood under conditioning, process of evaporating solvent. The amount of the diffusion is known to be determined by the solute diffusivity and the solute-concentration difference between cell walls and cell cavities. Purpose of this paper was to clarify the effect of temperature only on the solute diffusivity that is directionally related to the thermal vibration of the solute molecule. The cross-cut block of hinoki (Chamaecyparis obtusa), polyethylene glycol (PEG1540), and water was employed as wood sample, solute, and solvent, respectively. The sample impregnated with a 20 mass% solution was conditioned at 20, 35, or 50 °C to finish the solute diffusion evaluated using the dimension of the sample that was conditioned followed by drying in a vacuum. To unify the solute-concentration difference, for all temperatures, the equilibrium moisture content was unified and the solvent-evaporation rate was controlled in three ways during conditioning. The solute diffusivity was higher in order of 35, 50, and 20 °C, which was evaluated by the solute diffusion at the same evaporation rate. It is clarified that the diffusivity increases with increasing the dimension of cell walls rather than with increasing the thermal vibration of solute molecule.  相似文献   

15.
Summary The effects of heating cork in water vapour at 100°C and 300°C are studied and compared with those produced by heating in air at the same temperatures. Dimensional and mass changes were measured and radial compression curves were obtained following various treatments. The 300°C treatments originate a straightening of the originally corrugated cell walls, while the cell wall material undergoes thermal degradation. Larger swellings and larger mass changes are observed in the treatments in water vapour as compared to those in air. The 100°C treatments do not induce degradation and produce reversible changes in technological properties which are simply due to differences in the water content.  相似文献   

16.
The effects of short-term thermomechanical (STTM) densification temperature and pressure on the changes in surface roughness, wettability, mass loss (ML), thickness and density of alder, beech, birch, and pine wood veneer with low moisture content (~5%) were investigated. The anatomical structure of veneers was also observed. Veneer sheets were densified using pressure levels of 4, 8 and 12 MPa at three temperatures: 100°C, 150°C and 200°C for 4 min. The results were compared with those of the non-densified veneers. The obtained results show that STTM densification of veneers similarly to long-term densification of solid wood causes irreversible changes in their properties. The STTM-densified veneer surfaces became smoother and more hydrophobic, ML increased slightly while roughness and thickness values decreased significantly, the cell lumens collapsed and a certain amount of fractures in cell walls developed with increasing densification temperature and pressure. All of the investigated wood species showed higher density values after densification. It was found that an even STTM densification of veneers provides stable properties under normal atmosphere conditions; in particular, the thickness and contact angle values were stable for 24 hours after densification, which is an important consideration for industrial applications.  相似文献   

17.
Summary Samples of Southern Pine (Pinus spp.) charred to 250°, 300°, 350°, 400° or 600°C in a flowing nitrogen atmosphere at rates of 1°, 10° and 50°C/min were examined using the scanning electron microscope to quantify changes in cross-sectional tracheid dimensions. The disappearance of discrete cell wall layers was time-dependent as opposed to strictly temperature-dependent. Tracheid diameters decreased in response to temperature and charring rate. Double cell wall thickness values also decreased in response to charring. This shrinkage was nearly isotropic. Below 300°C, latewood cells were more stable than earlywood cells. Above 300°C, the reverse was true. This was attributed to the probable circumferential arrangement of cellulose, hemicellulose, and lignin within the cell wall. The highest rate of thermal degradation was between 300° and 350°C.The sample material was prepared by F. C. Beall and D. H. Slocum at the University of TorontoThe authors are Assistant Professor of Forestry, Professor of Biological Sciences and Professor of Forestry, respectively, at the University of Missouri-Columbia, Columbia  相似文献   

18.
The morphology of charcoals was investigated by scanning electron microscopy. Charcoal of Quercus variabilis was prepared in an electric furnace under nitrogen gas atmosphere at 400, 600, 800 and 1,000°C. Charring temperature greatly affects the structure of charcoal. In charcoal prepared at 400°C, most of the morphological characteristics remained relatively unchanged with the exception of the cell-wall layering. The cell walls appeared homogenous and glass-like. Above 400°C, there was an increase in cell-wall thinning and volumetric shrinkage with an increase in the charring temperature. These two factors were responsible for most of the observed changes in structure. Fracture surfaces became increasingly rough and disrupted. Vessel elements were increasingly distorted and tyloses disintegrated with increases in temperature. Parenchyma cells exhibited greater shrinkage except at the pits. This resulted in the appearance of distinctive small protuberances over the surface of the parenchyma cells. Rhomboidal calcium crystals were found to be abundant at all the temperatures studied, but at 800 and 1,000°C the crystals had a sponge-like appearance.  相似文献   

19.
We evaluated the antifungal and antitermite activities of wood vinegars produced from oil palm trunk. The wood vinegars were produced at three different pyrolysis temperatures, 350, 400, and 450 °C. Antifungal activities of vinegars were evaluated using a Petri dish bioassay with 0.5, 1.0, and 1.5% (v/v) against a white-rot fungus, Trametes versicolor, and a brown-rot fungus, Fomitopsis palustris. Antitermite activities were tested using a no-choice bioassay method for Coptotermes formosanus with 2.5, 5.0, 7.5, and 10.0% (v/v). All the wood vinegars exhibited antifungal activities against T. versicolor. In particular, the wood vinegar produced at 350 °C resulted in complete inhibition of T. versicolor growth at 1.0 and 1.5%. However, higher concentrations were required to obtain growth inhibition of F. palustris. All the wood vinegars exhibited antitermite activity to C. formosanus workers in the no-choice experiment at relatively high concentrations. For instance, 10% concentration was required to achieve 100% mortality against C. formosanus at all production temperatures. The lowest mass loss of the treated filter paper of 11.75% was obtained with a 350 °C—10.0% combination.  相似文献   

20.
Sugi (Cryptomeria japonlca D. Don) wood powder was carbonized at varying temperatures by a onestep process up to 1000C and a two-step process using wood charcoal as the raw material up to 1600C. This study was conducted to evaluate the adsorptive properties of wood charcoal and discuss the mechanism of its adsorptive function in relation to the physical and anatomical characteristics of wood after carbonization. Anatomical characteristics of carbonized wood materials were directly observed under heating using an environmental scanning electron microscope (ESEM); the cell wall structures were analyzed by high-resolution transmission electron microscope (HRTEM). The largest weight losses were observed at the highest temperatures, in both the one-step and twostep processes but leveled off above 800C. Shrinkages in the tangential, radial, and longitudinal directions increased with carbonization temperature, peaking at 1000C. Direct observations by ESEM showed distinct shrinkage at around 400C. The first trial observations by HRTEM on the changes in the ultrastructure of cell walls of wood charcoals were done, and it was assumed to affect the formation of micropores. Adsorption was found to follow the Langmuir isotherm model. With the one-step carbonization process, the iodine adsorption capacities of the carbonized wood powders increased with increasing carbonization temperature, peaking at 800C, but decreased at higher temperatures. The wood powder carbonized at 1000C with the two-step process showed the highest capacity, but further heating up to 1400C drastically decreased the adsorption. The shrinkage of cells was related to the increases and decreases in its specific surface area. Specific surface area and total pore volume were evidently related to the adsorptive properties.Part of this paper was presented at the Second International Wood Science Seminar, Indonesia, November 6–7, 1998  相似文献   

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