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Series editors' preface - Wood Tools

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suppliers. Careful selection of solvent/s and<br />

delivery systems can greatly increase the specificity<br />

of a cleaning treatment and decrease the<br />

risk to the surface that is to be retained. By<br />

selecting solvents on the basis of, for example,<br />

volatility and relative compatibility to a<br />

surface, the speed and extent of action can be<br />

controlled. Solvents can be used on a wide<br />

range of dirt and surface types and can<br />

penetrate into otherwise inaccessible areas.<br />

Some of their disadvantages are their limited<br />

effect on very polar dirt, toxicity, flammability<br />

and expense. Factors influencing solvent<br />

choice include volatility, viscosity, surface<br />

tension (capillarity), toxicity, flammability and<br />

solubility parameters.<br />

Evaporation rates, vapour pressure and<br />

density<br />

The evaporation rate describes the rate at<br />

which a material will change from liquid to<br />

vapour, at a standard temperature and<br />

pressure, in comparison to the evaporation<br />

rate of a specific known material. The evaporation<br />

rate of a solvent is dependent on the<br />

size of the solvent molecules and the forces<br />

of attraction between them. A homologous<br />

series of compounds only differs from the next<br />

compound in the sequence by the addition of<br />

a CH 2 group, e.g. methane (CH 4), ethane<br />

(C 2H 6), propane (C 3H 8) etc. The smaller the<br />

molecule in any given homologous series, the<br />

lower the boiling point, the higher the vapour<br />

pressure and the faster its evaporation rate.<br />

Van der Waals forces are the predominant<br />

attractive force in hydrocarbon solvents. These<br />

are weak and as a result low molecular weight<br />

hydrocarbons are very volatile (e.g. methane,<br />

ethane and propane). As the molecules<br />

become larger they evaporate more slowly and<br />

when very large, aliphatic hydrocarbons form<br />

solid substances called paraffin waxes. An<br />

aromatic structure induces slight polarity in<br />

otherwise non-polar molecules and results in<br />

a comparative increase in boiling point and<br />

vapour pressure. Alcohols are polar molecules<br />

that also have considerable hydrogen bonding<br />

between them. As a result they are less volatile<br />

than similar-sized hydrocarbons. Hydrogen<br />

bonding is the dominant intermolecular force<br />

in water. Thus even though water is a small<br />

molecule, stronger intermolecular forces mean<br />

that, comparatively, its boiling point is high<br />

Principles of cleaning 513<br />

and its vapour pressure is low. Liquids that<br />

evaporate rapidly may be described as volatile.<br />

The evaporation rate of a single solvent is<br />

dependent on vapour pressure (in turn dependent<br />

on temperature and pressure), surface/<br />

volume ratio and the rate of air flow over the<br />

surface (Wicks et al., 1992).<br />

As a general rule, there is an inverse<br />

relationship between the boiling point of a<br />

solvent and its evaporation rate, i.e. the higher<br />

the boiling point, the lower the evaporation<br />

rate. Evaporation rates are usually expressed<br />

as a ratio and therefore do not have units of<br />

measurement. There are two widely used<br />

standard solvents, diethyl ether (ether) and nbutyl<br />

acetate (nBuAc), which are assigned a<br />

relative value of 1 or 100. Unfortunately, the<br />

scales are not interchangeable. A slow evaporation<br />

rate on the ether scale corresponds to<br />

a high number, i.e. the time a solvent takes to<br />

evaporate is many times that which ether<br />

takes. In contrast, a slow evaporation rate on<br />

the butyl scale corresponds to a low number,<br />

i.e. the evaporation rate is slower than that of<br />

butyl acetate. Evaporation rates may also be<br />

measured in ‘seconds to 90% evaporation’ (see<br />

Table 11.1).<br />

The vapour pressure of a solvent is a<br />

measure of the pressure exerted by its vapour<br />

when the solvent and its vapour are in dynamic<br />

equilibrium, i.e. when the molecules leaving a<br />

liquid to form vapour and those rejoining it are<br />

in equilibrium. Vapour pressure is measured in<br />

a closed vessel and at a standard temperature<br />

and pressure. As a general rule, there is an<br />

inverse relationship between the boiling point<br />

of a solvent and its vapour pressure, i.e. the<br />

higher the vapour pressure, the lower the<br />

boiling point and the faster the evaporation<br />

rate.<br />

Organic solvent vapours are heavier than air<br />

(i.e. their relative vapour density is higher than<br />

air). This is particularly important for ventilation<br />

and when dealing with spillages. Whilst<br />

extraction should draw solvent fumes away<br />

from the conservator, ventilation should be<br />

designed to draw from, and tests for toxic<br />

concentrations may need to be made at, floor<br />

level.<br />

Viscosity<br />

Viscosity describes the resistance to flow of a<br />

liquid. It is a result of the size and shape (e.g.

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