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Series editors' preface - Wood Tools

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76 Conservation of Furniture<br />

cules, the apparent groupings referred to as fibrils<br />

(sub-groupings sometimes termed micro fibrils).<br />

It is the orientation of fibrils which defines<br />

the layering of the secondary wall. Within the<br />

thinner S 1 and S 3 layers, the fibril orientation is<br />

nearly perpendicular to the cell axis, whereas<br />

fibrils within the dominant S 2 layer are oriented<br />

more nearly parallel with the cell axis.<br />

Experimental evidence provides a theoretical<br />

explanation of the arrangement of cellulose<br />

within fibrils. In random areas, called crystallites,<br />

cellulose molecules (or more likely, portions<br />

of cellulose molecules) are aligned into<br />

compact crystalline arrangement. Adjacent<br />

areas where cellulose is non-parallel are called<br />

amorphous regions. The hemicelluloses and<br />

lignin are also dispersed between crystallites<br />

and through the amorphous regions.<br />

Within the fibrils, water molecules cannot<br />

penetrate or disarrange the crystallites. Water<br />

molecules can, however, be adsorbed by<br />

hydrogen bonding in one or more layers to the<br />

exposed surfaces of crystallites and components<br />

of amorphous regions, namely at the sites<br />

of available hydroxyl groups. Such polar groups<br />

of the polysaccharide fractions on exposed wall<br />

surfaces provide the principal active sites for<br />

bonding of adhesives and finishes and for other<br />

chemical reactions with wood.<br />

Because the average length of cellulose molecules<br />

is far greater than the apparent length of<br />

the crystallites, it is concluded that an individual<br />

cellulose molecule may extend through<br />

more than one crystalline region, being incorporated<br />

in crystal arrangement at various<br />

points along its total length. Therefore, within<br />

the fibrillar network, the random end-wise<br />

connection of crystallites would appear to offer<br />

linear strength to the fibril. Since crystallites<br />

would be more readily displaced laterally from<br />

one another due to the intrusion or loss of<br />

water molecules (or other chemicals capable of<br />

entering the fibrils), dimensional response<br />

would be expected perpendicular to the fibril<br />

direction. In summary, the linear organization<br />

of cellulose within the fibrils, the dominance of<br />

the S 2 layer, and the near-axial orientation of<br />

fibrils within the S 2 layer, together provides a<br />

foundation of understanding of the greater<br />

strength and dimensional stability of the cell in<br />

its longitudinal direction. It follows that wood<br />

itself – as the composite of its countless cells –<br />

has oriented properties.<br />

2.4 <strong>Wood</strong>–water relations and<br />

movement<br />

No other area of wood science and technology<br />

is more important to object conservation than<br />

wood–moisture relationships. The moisture<br />

condition of wood is related to properties ranging<br />

from thermal conductivity and strength to<br />

adhesive bonding and fungal development.<br />

However, the most telling influence of moisture<br />

in wood is upon dimensional behaviour.<br />

Solving and preventing the array of problems<br />

related to dimensional movement in wooden<br />

objects begins by recognizing the fundamental<br />

relationships involving wood, moisture and the<br />

atmosphere. It is customary to express the<br />

amount of water in wood as moisture content.<br />

The moisture content (MC) of wood is defined<br />

as the ratio of the weight of water in a given<br />

piece of wood to the weight of the wood when<br />

it is completely dry. The water-free weight of<br />

wood is also referred to as its oven-dry weight,<br />

determined by drying a wood specimen at<br />

100–105 °C until it ceases to lose weight.<br />

Moisture content is expressed as a percent and<br />

is calculated as follows:<br />

MC = Wi – Wod 100/Wod where<br />

MC = moisture content, expressed as a<br />

percentage<br />

Wi = initial weight<br />

Wod = oven-dry weight.<br />

Water exists in wood in two forms, as bound<br />

water and as free water. Water adsorbed and<br />

held within the cell wall by hydrogen bonding<br />

is called bound water. Water in wood in excess<br />

of the fibre saturation point exists as liquid<br />

water in the cell cavities and is called free<br />

water. The fibre saturation point (FSP) is the<br />

moisture condition of wood wherein the cell<br />

walls are completely saturated with bound<br />

water but the cell cavities are devoid of free<br />

water. It is usually expressed as a numerical<br />

value of moisture content and is generally in<br />

the range 25–30%.<br />

The sap contained in living trees is primarily<br />

water, with small amounts of dissolved minerals<br />

and nutrients. <strong>Wood</strong> in living trees is always<br />

above the fibre saturation point, although the<br />

moisture content may vary from slightly above<br />

the fibre saturation point to 200–300%,

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