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Outdoor performances of a polyurethane varnish and an alkyd-based synthetic varnish coated over chromium-copper-boron (CCB)-impregnated Scots pine (Pinus sylvestris L.) and chestnut (Castanea sativa Mill.) [10 (R) × 100 (T) × 150 (L) mm] were investigated. These varnishes were also applied to the wood surface as sole coatings or impregnated into wood as water-repellent (WR) solutions. Outdoor exposure was performed in the Black Sea region of northern Turkey (41°N, 39.43°E) where humid weather predominates throughout the year and accelerates decomposition of coated wood surfaces. The wood panels were exposed at 45 ° south on their tangential surfaces. After 9 months of exposure to summer, autumn, and the following winter season, the color and glossiness changes of the exposed surface, adhesion of the coating layer to the wood surface, water absorption through the coating layers, mass loss, and the hardness of the board surface were studied. CCB impregnation greatly stabilized the surface color of varnish-coated panels of both wood species. Gradual decreases of adhesion between varnished layers and preimpregnated surfaces were attributed to probable weakening of interactions at the interface of the treated wood and the film layer. A superficial cleaning process of treated wood is suggested to improve glossiness and adhesion. The coated wood surface became harder with time on outdoor exposure until a maximum hardness occurred followed by softening, whereas the uncoated surface softened steadily. Polyurethane varnish yielded a harder surface than synthetic varnish. Mass losses of wood panels after 9 months of exposure were negligible for all treatments compared with the untreated controls, which were

Japanese cedar (Cryptomeria japonica) preheated at 700°C was subsequently heated to 1800°C and characterized by electron microscopy, X-ray diffraction, and micro-Raman spectroscopy. The degree of disorder of carbon crystallites and the amount of amorphous phase decreased considerably with an increase in heat treatment temperature to 1400°C, while carbon crystallites clearly developed above this temperature, showing that the microstructure of carbonized wood undergoes drastic changes around 1400°C. Besides showing the bands for sp 2 -bonded carbon, the Raman spectra showed a shoulder near 1100 cm −1 assigned to sp 3 -bonded carbon. With an increase of heat treatment temperature, the peak position of the Raman sp 3 band shifted to a lower frequency from 1190 to 1120 cm −1 , which is due to the transformation of sp 3 -bonded carbon from an amorphous phase to a nanocrystalline phase. These data showed that the microstructure of carbonized wood from 700° to 1800°C consisted of the combination of sp 2 -and sp 3 -bonded carbon, which is probably due to the disordered microstructure of carbonized wood. It is suggested that the sp 3 -bonded carbon is transformed from an amorphous structure to a nanocrystalline structure with the growth of polyaromatic stacks at temperatures above 1400°C.

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