water vapour sorption properties of Sitka spruce determined using a dynamic vapour sorption apparatus

• Published in: Wood science and technology Vol. 44; no. 3; pp. 497 - 514
• Main Authors: Hill, Callum A. S, Norton, Andrew J, Newman, Gary
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Berlin/Heidelberg : Springer-Verlag 01.08.2010; Springer-Verlag; Springer Nature B.V
• Subjects: Adsorption; Biomedical and Life Sciences; Ceramics; Composites; Desorption; Fibers; Food plants; foods; Glass; Glass transition temperature; heat; hysteresis; Hysteresis loops; Isotherms; Kinetics; Life Sciences; Machines; Manufacturing; Natural Materials; Original; Picea abies; Picea sitchensis; plant fibers; Processes; Relative humidity; Sorption; Temperature; Temperature dependence; Temperature effects; Transition temperatures; Vapors; Vegetable fibers; Water vapor; Wetting; wood; Wood Science & Technology; Equilibrium Moisture Content; Desorption Curve; Moisture Content; Fibre Saturation Point; Wood Cell Wall
• ISSN: 0043-7719; 1432-5225
• DOI: 10.1007/s00226-010-0305-y

The water vapour sorption properties of Sitka spruce (Picea abies) have been investigated over a range of temperatures (14.2-43.8°C) using a dynamic vapour sorption apparatus. The sorption kinetics behaviour was evaluated using the parallel exponential kinetics model which has been found to give very accurate fits to the data in studies of foodstuffs or plant fibres, but has not been previously applied to sorption studies with wood. Both the adsorption and desorption kinetics curve can be deconvoluted into a fast and slow exponential process. Under conditions of adsorption, the fast process appears to be associated with the formation of monolayer water (determined using the Hailwood Horrobin model) up to a relative humidity of 20%. Under desorption, there is no clear differentiation between fast and slow processes. The area bounded by the sorption hysteresis loop reduced as the temperature at which the isotherm was measured increased, due to movement of the desorption curve only, with the adsorption curve remaining the same at all temperatures. This behaviour is consistent with sorption processes taking place on nanoporous glassy solids below the glass transition temperature. The heat of wetting was determined from the temperature dependence of the desorption isotherms by using the Clausius-Clapeyron equation, yielding results that are consistent with literature values. However, doubts are raised in this paper as to the applicability of using the Clausius-Clapeyron equation for analyses of this type.