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Sticker stain is a material defect that results from moisture migration during wood drying, often spoiling the appearance of the surface of wood products. The effect of drying temperatures on the occurrence of surface sticker stain was investigated using Japanese cedar (Cryptomeria japonica D. Don) and three types of stickers (air-dried Japanese cedar, aluminum, and stainless steel) under four drying temperatures (20°C, 50°C, 75°C, and 100°C). At lower drying temperatures, the air-dried wood sticker tended to suppress the occurrence of surface sticker stains, whereas higher temperature or metal stickers produced sticker stains with deep color. However, no definitive relation was shown between the initial moisture content and the extent of sticker stain with deep color regardless of drying temperatures. It was considered that the partial delay of drying happened around the contact area with stickers, especially in cases of metal stickers. It was also found that the use of metal stickers at higher drying temperatures induced depressions in Fourier transform infrared spectra related to the occurrence of hygrothermal conditions.

Since wood chemical components can be depolymerized and modified by weathering, a better understanding of the mechanisms governing these processes in needed to develop effective protection methods for wood surfaces. Unfortunately, very little has been reported about the micro-scale chemical changes in wood, particularly hardwood, during weathering. The purpose of the present work is to determine the degradation behavior of Japanese beech (Fagus crenata Blume) under artificial weathering at the cellular-level. Herein, the structural and micro-distributional changes in wood components during weathering were investigated using micro-Raman spectral and chemical mapping analyses. The Raman spectra showed that weathering facilitated lignin degradation and modification. The degradation behavior of lignin differed depending on the type of wood tissue. The rate of lignin reduction followed a descending order: vessel element > axial parenchyma cell > wood fiber. Raman mapping determined that cellular-level lignin reduction on the surface layers differed for wood species. Although lignin degradation of cedar tracheids proceeded from both the surface and the cell lumen, the lignin in beech fibers degraded according to the depth.

Cryptomeria japonica was treated with 90% pyridinium chloride ([Py]Cl) and 10% water w/w solution at 80 and 120 °C. Most hemicellulose in C. japonica was liquefied and over half the lignin in C. japonica was solubilized after treatments at 80 and 120 °C. However, cellulose was mostly insoluble at 80 °C and partially soluble at 120 °C. The crystal structure of cellulose in the cell walls was retained after treatment at 80 °C for 48 h. The degradation products from the polysaccharides were obtained in different yields. The 90% [Py]Cl and 10% water w/w solution is effective for the treatment of lignocellulosics, such as liquefaction of lignocellulosics and the production of useful low molecular weight compounds.

Changes in the ultrastructure and chemical components, and their distribution in Japanese beech (Fagus crenata), during the ionic liquid 1-ethylpyridinium bromide ([EtPy][Br]) treatment were examined at the cellular level by light microscopy, scanning electron microscopy, and confocal Raman microscopy. Each of the tissues, including wood fibers, vessels and parenchyma cells treated with [EtPy][Br] showed specific morphological characteristics. Furthermore, lignin can be preferentially liquefied and eluted in [EtPy][Br] from the cell walls when compared to polysaccharides. However, the delignification was heterogeneous on the cell walls as lignin maintained a relatively high-concentration at the compound middle lamella, cell corners, inner surface of the secondary wall, and pits after [EtPy][Br] treatment.

The distribution of wood preservative coatings in wood surface layer was assessed at the cellular level using confocal Raman microscopy. Raman images were created based on the fingerprint Raman bands of the different wood polymers and coating components (resin and pigment). The wood cell walls and the distribution of the resin and pigment were clearly visualized at the same time. It was concluded that confocal Raman microscopy is suitable for the evaluation of the microdistribution of wood coatings, providing valuable information for the improvement of wood coating technology.

Three hardwoods of varying vessel arrangement were treated with the ionic liquid, 1-ethyl-3-methylimidazolium chloride ([C2mim][Cl]), which can dissolve cellulose, to investigate its influence on wood tissue morphology. Characterization was carried out by light and scanning electron microscopy. The wood fibers of all species swelled significantly during [C2mim][Cl] treatment. The swelling behavior varied according to wood species and differed from other cell types such as ray parenchyma cells. Morphological changes of the pits also varied between wood species. Treatment with [C2mim][Cl] affects wood tissues differently depending on wood species and cell type. These differences are not due to the vessel arrangement and its presence, but possibly from the chemical component and the microfibril angle of various wood tissues.

The morphological changes in wood tissues of Japanese beech (Fagus crenata) upon treatment with the ionic liquid, 1-ethyl-3-methylimidazolium chloride ([C2mim][Cl]), which can dissolve cellulose, were investigated. Treatment with [C2mim][Cl] induced significant swelling of all wood tissues. However, the swelling behavior of wood fibers was different from that of vessels. Intervascular pits were occluded, and pit membranes in ray-vessel pits were broken after treatment with [C2mim][Cl]. No significant differences in swelling behavior were found between latewood and earlywood, although different morphological changes for latewood and earlywood during [C2mim][Cl] treatment were seen in our previous studies on sugi (Cryptomeria japonica). We have found that the effects of [C2mim][Cl] on Japanese beech tissues are inhomogeneous and different from those found for other wood species.

The morphological and topochemical changes in wood tissues in compression wood of Japanese cedar (Cryptomeria japonica) upon treated with two types of ionic liquids, 1-ethyl-3-methylimidazolium chloride ([C2mim][Cl]) and 1-ethylpyridinium bromide ([EtPy][Br]) were investigated. Compression wood tracheids were swollen by both ionic liquids but their swelling behaviors were different in the types of ionic liquids used. Under the polarized light, we confirmed that crystalline cellulose in compression wood is amorphized by [C2mim][Cl] treatment whereas it changes slightly by [EtPy][Br] treatment. Raman microscopic analyses revealed that [C2mim][Cl] can preferentially liquefy polysaccharides in compression wood whereas [EtPy][Br] liquefy lignin. In addition, the interaction of compression wood with ionic liquids is different for the morphological regions. These results will assist in the use of ionic liquid treatment of woody biomass to produce valuable chemicals, bio-fuels, bio-based composites and other products.