Abstract

Water vapor sorption is the most fundamental aspect of wood-moisture relations. It is directly or indirectly related to the physical properties of wood and the onset of wood-damage mechanisms. While sorption properties of cellulosic materials have been utilized since antiquity, the time-dependent transition from one moisture content to another (i.e., sorption kinetics) has received much less attention. In this critical review, we present the state-of-the-art of water vapor sorption kinetics in wood. We first examine different experimental methods that have been used to measure sorption kinetics, from the quartz helix vacuum balance beginning in earnest in the 1930s, to automated sorption balances used recently. We then give an overview of experimental observations and describe the physical phenomena that occur during the sorption process, which potentially govern the following kinetics: boundary layer mass transfer resistance, heat of sorption, cell wall diffusion, swelling, and polymer mobility. Finally, we evaluate theoretical models that have been proposed for describing sorption kinetics, considering both experimental data and the physical processes described in the previous section. It is clear that no previously developed model can phenomenologically describe the sorption process. Instead, new models are needed. We conclude that the development of new models will require more than simple gravimetric measurements. In addition to mass changes, complementary techniques are needed to probe other important physical quantities on multiple length scales.

Highlights

  • As a building material, wood is unique in that its strength and stiffness, and even its dimensions, are strongly dependent on moisture

  • Advantages of the vacuum sorption apparatus include the following: mass measurements are made in situ, so the specimen is not disturbed, and multiple specimens can be monitored in parallel; vapor pressure can be changed rapidly and maintained at a stable value; vapor pressure stability is dependent on temperature stability, which has been reported to range from ±0.01 ◦ C [34,35] to

  • This paper summarizes the current state of knowledge of water vapor sorption kinetics

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Summary

Introduction

Wood is unique in that its strength and stiffness, and even its dimensions, are strongly dependent on moisture. Of the total mass of moisture in the wood to the mass of the dry wood; it is not a weight fraction of refers to the change in phase of a water molecule from the vapor phase to a condensed phase in moisture, and moisture contents of over 100% are possible. The sorption process involves the creation or disruption of strong in phase of a water molecule from the vapor phase to a condensed phase in wood (or vice versa). It should be noted that in much of with the wood polymers and “desorption” is the process by which absorbed moisture moves into the wood science literature, the absorption of water vapor is often referred to as “adsorption”.

Overview
Conditioning Chamber
Desiccator with Aqueous Solution
Quartz Helix Vacuum Balance
Automated Vacuum Balance
Automated Continuous-Flow Sorption Balance
Summary of Main Experimental Observations on Sorption Kinetics
Absorption curves measured with a vacuum sorption balance forbalance
Absorption Versus Desorption
Temperature
Physical
External Resistance to Vapor Transfer
Temperature Change
Diffusion of Bound Water within Cell Walls
Dimensional Changes and Associated Stresses
Polymer Mobility
Fickian Diffusion Model
Sorption curves as predicted byby
Swelling Stress Models
Thermally Limited Moisture Transport Model
The model partitions change into “fast”
Conclusions and Perspective on Research Needs
Results

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