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Chemical Composition and Related Properties of Lime (Tilia cordata Mill.) Bark and Wood as Affected by Tree Growth Conditions
Tilia cordata Mill. is a favourite tree used in urban spaces. For this reason, it is important to know its sensitivity to environmental stress, which is particularly burdensome for vegetation in urban spaces. The aim of the study was to investigate the properties necessary to control the growth of these trees and their subsequent use, i.e., chemical properties (percentage contents of cellulose, holocellulose, lignin, pentosans and substances soluble in NaOH and EtOH) as well as the chemical elements (K, Na, Mg, Ca and Fe, Zn, Cu, Pb, Cd, B, Ni, Cr, Al, As and Hg) and selected hygroscopic properties (hysteresis and sorption isotherms). Trees of Tilia cordata Mill. growing in environments exposed to environmental stress of varying severity were examined. Regardless of the growth conditions, in terms of its chemical composition, bark differs significantly from wood, showing twice the contents of soluble substances in NaOH and lignin and half the content of polysaccharides. Growth conditions clearly affect the range of selected chemical components in bark, e.g., substances soluble in ethanol, cellulose, or lignin. The main inorganic elements in bark and wood are Na, K, Ca, Mg and Zn. In bark, a relationship was found between the content of most chemical elements and differing environmental growth conditions. It was shown that environmental stress influenced the hygroscopic properties of wood and bark, which are a consequence of the percentage of chemical components.
Initial Desorption of Reaction Beech Wood
The research aimed to obtain empirical data for modeling the initial desorption in reaction wood from the cross-section of the green beech (Fagus sylvatica L.) log. Firstly, we analyzed the chemical composition, macro and microscopic structure of tension and opposite wood tissue. Then, the Equilibrium Moisture Content (EMC) was measured by the Dynamic Vapor Sorption method during the initial desorption. The used air parameters were specific for the mild drying schedule of green beech timber (t = 20, 35, and 50 °C, Relative Humidity (RH) ranging from 95 to 0 %). Relationships between the EMC of reaction wood and drying parameters were modeled using the Response Surface Method (RSM). The tests revealed: different hygroscopic properties of tension and opposite wood, the dependence of EMC value on temperature, and differences between EMC values for initial (first) and second desorption. Moreover, it was confirmed that, during initial desorption, the EMCs of reaction wood are significantly higher than reference EMC data. The differences in the EMC value are up to 0.14 kg/kg (for air with RH above 90 %). The presented polynomial model of the initial desorption of reaction beech wood can improve drying schedules for beech sawn timber with a high amount of reaction tissue.
Interlaboratory study of automated sorption measurements in wood: method for correcting systematic errors with the commonly used 0.002% min−1 stop criterion
Abstract Many studies that use an automated sorption balance to determine a water vapor sorption isotherm for wood collect data until the moisture content change is less than or equal to 0.002% min−1 (20 µg g−1 min−1). This stop criterion has been claimed to give errors in equilibrium moisture content (EMC) predictions of less than 0.001 g g−1 but over the past 10 years, studies have shown that the actual errors can be greater than 0.01 g g−1 because the measurements are stopped well before equilibrium is reached. Despite the large errors associated with this stop criterion, it remains popular due to the speed at which isotherms can be measured. This paper utilizes data from a worldwide interlaboratory study on automated sorption balances to develop a correction method for estimating EMC of western larch (Larix occidentalis Nutt.) from the moisture content corresponding to the 20 µg g−1 min−1 criterion. The study uses data from 72 relative humidity absorption steps with hold times of 7–10 days from 21 different laboratories and eight different instrument models. EMC is defined based on the inherent mass stability of automated sorption balances determined in the first part of this interlaboratory study. On average the sorption process is less than 80% complete when the 20 µg g−1 min−1 criterion is reached, resulting in a mean absolute error (MAE) of 0.006 g g−1. The correction equation for estimating EMC reduces the MAE to 0.001 g g−1. The analysis presented in this paper, along with the correction equation, can be considered for certain use cases to reduce systematic errors and shorten measurement times.