Mechanical interaction between cellulose microfibril and matrix substance in wood cell wall determined by X-ray diffraction

2005 ◽  
Vol 51 (4) ◽  
pp. 334-338 ◽  
Author(s):  
Kentaro Abe ◽  
Hiroyuki Yamamoto
Cellulose ◽  
2013 ◽  
Vol 20 (2) ◽  
pp. 633-643 ◽  
Author(s):  
Keisuke Toba ◽  
Hiroyuki Yamamoto ◽  
Masato Yoshida

2021 ◽  
Author(s):  
◽  
Stefan James Hill

<p>The mechanical properties of wood allow it to be used for numerous purposes. For most purposes, drying of the wood material from the green state, sawn from the log, is first required. This drying step significantly improves the strength properties of wood. It is therefore clear that moisture in wood plays an important role in determining the bulk mechanical properties. Over the last century, many studies have been carried out to investigate the way in which the water content wood affects the bulk mechanical properties. More recent studies have focused to the individual chemical components that make up wood to understand the observed changes in bulk mechanical properties. Models of the nanostructure of wood contained; cellulose, hemicellulose, and lignin, and the arrangement and location of these components in terms of their mechanical properties was interpreted through what was described as the 'slip-stick' mechanism, by which wood, in its green state, maintained its molecular and mechanical properties under external stresses. This model, while insightful, failed to account for the presence and the role of water in the nanostructure of wood. In this work, synchrotron based X-ray diffraction and NMR studies, have been used to develop a new model, in which water plays a vital role in the determination of the mechanical properties of wood in its green, part-dried, and rewet states. X-ray diffraction showed that changes occur to the molecular packing of cellulose crystallites with change in moisture content, and that these changes begin to occur under mild drying conditions, i.e. drying in air at ambient temperatures. These changes depend on the severity of drying, whether ambient or forced oven drying, and are to some extent reversible. A spin-diffusion model was constructed using dimensions obtained from Xray diffraction, comparisons between predictions and experimental data from an NMR study showed that the location of water was dependent on the moisture history of wood. In the green state, at least some of the water in the wood cell wall forms a layer, between the cellulose crystals and the hemicellulose and lignin matrix. If dried and then rewet, this water associated with the cellulose crystals was not present to the same degree as in the green state, allowing a closer association of the hemicellulose with the cellulose. The effect of this change in water distribution in the wood cell wall on the bulk mechanical wood properties was shown in mechanical testing. The nanostructure of the wood cell wall therefore should be considered to contain cellulose, hemicellulose, lignin and water, where each component contributes, according to its molecular properties, dynamic mechanical properties which are reflected in the bulk material properties.</p>


2021 ◽  
Author(s):  
◽  
Stefan James Hill

<p>The mechanical properties of wood allow it to be used for numerous purposes. For most purposes, drying of the wood material from the green state, sawn from the log, is first required. This drying step significantly improves the strength properties of wood. It is therefore clear that moisture in wood plays an important role in determining the bulk mechanical properties. Over the last century, many studies have been carried out to investigate the way in which the water content wood affects the bulk mechanical properties. More recent studies have focused to the individual chemical components that make up wood to understand the observed changes in bulk mechanical properties. Models of the nanostructure of wood contained; cellulose, hemicellulose, and lignin, and the arrangement and location of these components in terms of their mechanical properties was interpreted through what was described as the 'slip-stick' mechanism, by which wood, in its green state, maintained its molecular and mechanical properties under external stresses. This model, while insightful, failed to account for the presence and the role of water in the nanostructure of wood. In this work, synchrotron based X-ray diffraction and NMR studies, have been used to develop a new model, in which water plays a vital role in the determination of the mechanical properties of wood in its green, part-dried, and rewet states. X-ray diffraction showed that changes occur to the molecular packing of cellulose crystallites with change in moisture content, and that these changes begin to occur under mild drying conditions, i.e. drying in air at ambient temperatures. These changes depend on the severity of drying, whether ambient or forced oven drying, and are to some extent reversible. A spin-diffusion model was constructed using dimensions obtained from Xray diffraction, comparisons between predictions and experimental data from an NMR study showed that the location of water was dependent on the moisture history of wood. In the green state, at least some of the water in the wood cell wall forms a layer, between the cellulose crystals and the hemicellulose and lignin matrix. If dried and then rewet, this water associated with the cellulose crystals was not present to the same degree as in the green state, allowing a closer association of the hemicellulose with the cellulose. The effect of this change in water distribution in the wood cell wall on the bulk mechanical wood properties was shown in mechanical testing. The nanostructure of the wood cell wall therefore should be considered to contain cellulose, hemicellulose, lignin and water, where each component contributes, according to its molecular properties, dynamic mechanical properties which are reflected in the bulk material properties.</p>


The cell-wall structure of the red alga Rhodymenia palmata has been examined by the methods of X -ray diffraction analysis and electron microscopy, including ultra-thin sectioning. The cell wall is shown to consist of numerous lamellae each of which is made up of unoriented, crystalline microfibrils embedded in an amorphous matrix of other cell-wall constituents. The material can be stretched reversibly up to 100% when wet, and the stretching induces orientation of the microfibrils. The ‘∝ cellulose' fraction, which accounts for only 2 to 7 % of the original dry weight, was isolated chemically and was analyzed by means of hydrolysis and paper chromatographic separation of the resulting sugars, and it was found to be composed of approximately equal quantities of glucose and xylose residues. Chemical treatment of the cell wall was found to cause considerable variations in the X -ray diagrams, which are discussed. It is concluded that the microfibrils contain both glucose and xylose residues in approximately equal proportions and that chemical treatment in this case causes changes in crystallinity of the structural component of the wall. The importance of these findings for the meaning of the term cellulose is discussed. The X -ray diagram of older fronds was found to be complicated by the occurrence of extra rings due to the presence of floridean starch, and the highly elastic properties of the thallus enabled the diagrams of the starch and the cell wall to be separated.


Holzforschung ◽  
2017 ◽  
Vol 71 (2) ◽  
pp. 129-135 ◽  
Author(s):  
Yanjun Li ◽  
Chengjian Huang ◽  
Li Wang ◽  
Siqun Wang ◽  
Xinzhou Wang

Abstract The effects of thermal treatment of bamboo at 130, 150, 170, and 190°C for 2, 4, and 6 h were investigated in terms of changes in chemical composition, cellulose crystallinity, and mechanical behavior of the cell-wall level by means of wet chemical analysis, X-ray diffraction (XRD), and nanoindentation (NI). Particularly, the reduced elastic modulus (Er), hardness (H), and creep behavior were in focus. Both the temperature and treatment time showed significant effects. Expectedly, the hemicelluloses were degraded and the relative lignin content was elevated, while the crystallinity of the cellulose moiety was increased upon thermal treatment. The Er and H data of the cell wall were increased after 6 h treatment at 190°C, from 18.4 to 22.0 GPa and from 0.45 to 0.65 GPa, respectively. The thermal treatment led to a decrease of the creep ratio (CIT) under the same conditions by ca. 28%. The indentation strain state (εi) also decreased significantly after thermal treatment during the load-holding stage.


Holzforschung ◽  
2019 ◽  
Vol 73 (7) ◽  
pp. 613-619 ◽  
Author(s):  
Chang-Goo Lee ◽  
Mariko Yamasaki ◽  
Takanori Sugimoto ◽  
Yasutoshi Sasaki

Abstract Synchrotron radiation X-ray diffraction (XRD) was applied to determine the cellulose content in 5-mm-thick sections of the annual rings of Japanese red pine (Pinus densiflora). Recent samples (air-dried in the last few years) and aged samples (250 years old) were investigated; the cellulose content in the S2 layer was measured by the transmission (Trs) method and that in the S1 and S3 layers by the reflection (Ref) method. Measurements were performed in the cellulose (004) Ref plane. The two XRD methods resulted in very different two-dimensional (2D) diffraction patterns, indicating differences in the cellulose characteristics. Azimuthal angle profiles showed cellulose chains measured by the Trs and the Ref methods oriented at about 9° and 75°, respectively, in terms of the longitudinal axis of the specimens. Moreover, 2θ profiles obtained by the Ref method had full-width-at-half-maximum (FWHM) values ≈3.5 times greater than the corresponding Trs profiles, indicating large variations in the cellulose lattice spacing d004. The 250 years of aging had no effect on the cellulose contents.


A general survey of cell-wall structure in the red algae has been carried out using the methods of X -ray diffraction analysis and electron microscopy. The fifteen species all show a similar wall structure consisting of numerous lamellae each of which is made up of random micro-fibrils embedded in an amorphous matrix. The X -ray diagrams obtained from several species are complicated by the existence of crystalline floridean starch, but nevertheless reveal the absence of cellulose I.


1979 ◽  
Vol 27 (4) ◽  
pp. 377 ◽  
Author(s):  
G Scurfield

Light microscopy, scanning electron microscopy, X-ray diffraction and differential thermal analysis have been used to examine the structure and mineralogical make-up of 79 Australian petrified woods. Initiation of petrifaction appears to rely on the provision of a substrate with inherent porosity, with the substrate components chemically rather inert and only slowly degraded at normal temperatures and pressures under conditions probably most often acid and tending to anaerobic, and the pores sufficiently large to allow access of an appropriate mineral in ionic or colloidal form in water. Stages in the process include entry of mineral solution into the wood via splits or checks, cell lumina, and other voids; permeation of cell walls; progressive dissolution of cell wall components beginning largely with lignin and accompanied by a build-up of a mineral framework adequate for maintaining the dimensional stability of the wood; mineral deposition in cell lumina after cell wall replacement as a continuous, intermittent, perhaps separate, but not obligatory event; mineral deposition in voids present or formed by dissolution of intercellular substance as a separate, but not obligatory event; and final lithification involving loss of water and perhaps replacement of one mineral by another.


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