Molecular sieving behavior of carbonized wood: selective adsorption of toluene from a gas mixture containing α-pinene.

The adsorption properties of wood carbonized at various temperatures were investigated using a mixed gas containing toluene and α-pinene. Hinoki (Chamaecyparis obtusa) samples carbonized at 500°–1100°C were exposed to gas mixtures of toluene and α-pinene at 20°C. The samples carbonized at 500°–700°C only adsorbed toluene, whereas those carbonized at 800°–1100°C adsorbed both toluene and α-pinene. Analysis of the surface structure of the carbonized wood by nitrogen adsorption at liquid nitrogen temperature indicated that the sample carbonized at 700°C had micropores mainly 0.6 nm in diameter and few mesopores, whereas the samples carbonized at 900°C and 1100°C had mesopores and micropores larger than 0.8 nm in diameter. With the sample carbonized at 700°C, the flatshaped toluene molecules could probably penetrate into the narrower pores, 0.8 nm in diameter, whereas the bulky globular-shaped α-pinene molecules could not. Carbonization at temperatures higher than 900°C probably enlarged the pore size and thereby reduced the selectivity of adsorption. The results revealed that wood carbonized below activation temperature has a unique fl at-pore structure that seems to work as a kind of molecular sieving carbon, successfully removing only the harmful volatile organic compound (VOC), toluene, and leaving behind a pleasant aroma of α-pinene in the atmosphere. [ABSTRACT FROM AUTHOR]