Seppo Andersson

Crystallinity of wood and the size of cellulose crystallites in Norway spruce (Picea abies)

X-ray diffraction was used to study variations in the crystallinity of wood and the average thickness and length of the crystallites of cellulose as a function of the number of the year ring in Norway spruce [Picea abies (L.) Karst.]. The crystallinity increased from ring 4 to ring 10 from the pith and was constant after ring 10. The crystallinity of mature wood was about 30% ± 5%. The average thickness and average length of the crystallites were 3.2 ± 0.1 nm and 28 ± 2 nm, respectively; and no systematic variation of these values with the number of the year ring was observed. The mean microfibril angle decreased near the pith but was constant in the mature wood.

Microfibril angle of Norway spruce [Picea abies (L.) Karst.] compression wood: comparison of measuring techniques.

The structure of cellulose, especially the microfibril angles (MFAs), in compression wood of Norway spruce [Picea abies (L.) Karst.] was studied by wide- and small-angle X-ray scattering and polarizing microscopy. On the basis of the X-ray scattering experiments the average MF As of the cell wall layers S2 and S1 of the studied sample are 39‡ and 89‡, respectively; and the average diameter and length of the cellulose crystallites are 2.9 and 20.0nm, respectively. The average of the whole MFA distribution is shown to agree with the one obtained by polarizing microscopy of macerated fibers.

Effect of growth rate on mean microfibril angle and cross-sectional shape of tracheids of Norway spruce

The variation of the mean microfibril angle (MFA) and the shape of the cross-section of lumen with the distance from the pith in fast grown Norway spruce were studied by X-ray scattering and optical microscopy. The samples were from stems of a clone of Norway spruce [ Picea abies (L.) Karst.] grown in a fertile site at Nurmijärvi, southern Finland Both the mean MFA and the circularity index of the lumen of the fast-grown trees decreased more gradually as the distance from the pith increased than those in reference trees grown in a medium fertility site. However, in mature wood the mean MFA reached the same level in fast-grown trees as in reference trees (5°–10°) but the cross-sections of the cells remained more circular in fast-grown trees than in reference trees. The dependence of the mean MFA on the distance from the pith was similar for earlywood and latewood, but the values of the mean MFA of latewood were systematically smaller than those of earlywood. Two different X-ray diffraction geometries were compared from the points of view of biology and data analysis.

X-ray scattering studies of thermally modified Scots pine (Pinus sylvestris L.)

Abstract Wood is thermally modified by heating and steaming in order to change its properties, e.g., to improve the biological resistance and to increase the hardness of wood. The structure of thermally modified Scots pine (Pinus sylvestris) was studied using wide-angle, small-angle and ultra-small-angle X-ray scattering methods. Modification temperatures varied from 100 to 240°C. No marked changes in the microfibril angle distribution were observed. The mass fraction of crystalline cellulose in wood (the crystallinity of wood) and the size of cellulose crystallites increased above 150°C. After modification at 230°C for 4 h the thickness of the cellulose crystallites increased from 3.1 to 3.4 nm. Thermal modification had no effect on the orientation of the voids, but an increase in the porosity of the cell wall was observed. The distance between cellulose crystallites was approximately 4.7 nm in hydrated wood and a decrease in order between microfibrils was observed at 160–200°C.

A physico-chemical characterisation of new raw materials for microcrystalline cellulose manufacturing

A detailed physico-chemical characterisation of potential new cellulose sources (rice husk, hemp stalk, and coniferous needles), and microcrystalline cellulose (MCC) manufactured from them, was made in this work. The length and the width of the cellulose crystallites were determined by wide-angle X-ray scattering (WAXS), crystallinities were studied by means of WAXS and solid state cross polarisation magic angle spinning 13C nuclear magnetic resonance (NMR) spectroscopy, and the packing and the cross-sectional shape of the microfibrils were determined by small-angle X-ray scattering. When MCC was prepared from rice husks and hemp stalks an acceptable yield was obtained. Crystallinities obtained with solid state NMR spectroscopy and WAXS were highest for MCC prepared from hemp stalks, and lowest for rice husk MCC. The crystallite sizes of MCC samples studied in this work varied more than in those MCC samples which were prepared from conventional plant sources, and crystallite size and cellulose crystallinity were related. When taking into account rather high values of specific surface, hemp stalks and rice husks appear as a promising raw materials for MCC production.

The elemental composition, the microfibril angle distribution and the shape of the cell cross-section in Norway spruce xylem

Relationships between the elemental composition, the microfibril angle (MFA) distribution and the average shape of the cell cross-section of irrigated-fertilised and untreated Norway spruce (Picea abies [L.] Karst.) earlywood were studied. Sample material was obtained from Flakaliden, Sweden. The elemental composition was studied by determining the relative mass fractions of the elements P, S, Cl, K, Ca and Mn by X-ray fluorescence and by determining the mass absorption coefficients for X-rays. X-ray diffraction was used to determine the MFA distribution and the average shape of the cell cross-section. The latter was also determined by light microscopy. In transition from juvenile wood to mature wood, a decrease of the mode of the MFA distribution from 13°–24° to 3°–6° was connected to a change in the shape of the cell cross-section from circular to rectangular. The irrigation-fertilisation treatment caused no change in the MFA distribution or in the shape of the cell cross-section, whereas the mass absorption coefficient was higher and the density was smaller in irrigated-fertilised wood. Larger proportion of the elements S, Cl and K, but smaller proportion of the element Mn, were observed due to the treatment. The results indicate that the shape of the cell cross-section or the MFA distribution are not directly linked to the growth rate of tracheids or to the nutrient-element content in the xylem and only show notable changes as a function of the cambial age.

Changes in Nanostructure of Wood Cell Wall during Deformation

The excellent mechanical properties of wood arise from its cellular and cell wall structure. X-ray scattering, ultrasound, and mechanical testing is combined to study the effects of strain on crystalline cellulose in wood. Results for dry and re-moistened softwood samples are reviewed and new results are presented for native, never-dried samples of Silver birch. When softwood is stretched parallel to the cell axis, the mean microfibril angle diminishes significantly in compression wood, but only slightly in clear wood. The cellulose chains in the crystallites elongate and their distance diminishes. In the never-dried Silver birch samples, axial strain caused the mode of the microfibril angle distribution to slightly decrease from the initial value of 14 degrees to 12 degrees. Unlike in softwood, in never-dried birch crystalline cellulose showed auxetic tensile behaviour. The distance of the chains increased and the X-ray Poisson ratio νca was negative, -0.3 ± 0.2. Dehydration of never-dried Silver birch caused no difference to the microfibril angle distribution.

Cellulose structure and lignin distribution in normal and compression wood of the Maidenhair tree (Ginkgo biloba L.)

We studied in detail the mean microfibril angle and the width of cellulose crystals from the pith to the bark of a 15-year-old Maidenhair tree (Ginkgo biloba L.). The orientation of cellulose microfibrils with respect to the cell axis and the width and length of cellulose crystallites were determined using X-ray diffraction. Raman microscopy was used to compare the lignin distribution in the cell wall of normal/opposite and compression wood, which was found near the pith. Ginkgo biloba showed a relatively large mean microfibril angle, varying between 19° and 39° in the S2 layer, and the average width of cellulose crystallites was 3.1-3.2 nm. Mild compression wood without any intercellular spaces or helical cavities was observed near the pith. Slit-like bordered pit openings and a heavily lignified S2L layer confirmed the presence of compression wood. Ginkgo biloba showed typical features present in the juvenile wood of conifers. The microfibril angle remained large over the 14 annual rings. The entire stem disc, with a diameter of 18 cm, was considered to consist of juvenile wood. The properties of juvenile and compression wood as well as the cellulose orientation and crystalline width indicate that the wood formation of G. biloba is similar to that of modern conifers.