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Series editors' preface - Wood Tools

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700 Conservation of Furniture<br />

Many silver polishes contain a tarnish<br />

inhibitor. North (1980) reported that removing<br />

the tarnish layer that had formed after the<br />

application of a tarnish inhibitor required more<br />

effort and resulted in greater removal of silver.<br />

Tarnish inhibitors will fail eventually and the<br />

tarnish that then forms may be uneven. Lins<br />

(1989) found that a film of tarnish inhibitor<br />

resulted in a silver surface that could not be<br />

wetted easily, polished evenly or adequately<br />

lacquered.<br />

Silver dips are usually composed of a<br />

mineral or organic acid (e.g. sulphuric or<br />

formic acid) and a complexing agent such as<br />

thiourea (Brenner, 1953). It should be noted<br />

that silver sulphide has a pK sp of 49.2, which<br />

far exceeds the K f of most chelators with the<br />

metal ion (see section 11.5.5). Thiourea, for<br />

example, binds silver with a K f of only 13.1,<br />

thus the removal of silver sulphide is a result<br />

of acidic conditions rather than chelation.<br />

Although dips will dissolve tarnish, they tend<br />

to leave a rougher, more granular surface with<br />

a larger surface area than polishes (Selwyn<br />

and Costain, 1991). They may be applied to<br />

mounts in situ, using a swab, or mounts may<br />

be removed from the object and immersed.<br />

Contact with silver dip should be minimized<br />

to limit acidic attack of the surface of the<br />

metal. Silver dips have the advantage of being<br />

quick and sometimes avoid the need for<br />

mechanical removal of corrosion products.<br />

However, dips tend to be an all or nothing<br />

process and the ultra clean appearance<br />

produced may not be desirable. In some cases<br />

it may be necessary to use polish after an<br />

object has been dipped. Silver treated with dip<br />

retarnishes more quickly than that cleaned<br />

with polishes.<br />

Reshaping<br />

Silver/copper alloys are metastable. Copper, as<br />

well as unintentional metallic impurities, will<br />

often migrate to the grain boundaries over<br />

time, leading to a loss of malleability called<br />

precipitation hardening. Because of this effect,<br />

it is considered unwise to attempt mechanical<br />

straightening of objects over 100 years old,<br />

and in practice, less time may be needed to<br />

make an object unsuitable for cold reforming.<br />

The techniques of polymer casting and<br />

electrotyping are both suitable for supplying<br />

missing parts on silver objects.<br />

Prevention of tarnish<br />

Given that the primary mechanism for the<br />

formation of tarnish on silver is exposure to<br />

atmospheric pollutants, the exclusion or<br />

absorption of such pollutants should be given<br />

a high priority for furniture that incorporates<br />

silver components.<br />

Coatings<br />

Lacquering is probably the best means of<br />

protecting silver from tarnishing while on<br />

open display in period rooms, houses etc.<br />

Various organic coatings have been used but<br />

many conservators prefer the appearance of<br />

cellulose nitrate lacquers (e.g. Frigilene,<br />

Agateen) on highly polished historic silver.<br />

They level very well and a skilfully lacquered<br />

object cannot be distinguished from an<br />

uncoated piece.<br />

15.3.12 Lead<br />

Lead may be encountered in furniture, for<br />

example in lead linings to urns or wine<br />

coolers, or in the form of lead-based repairs.<br />

Lead is relatively inert. Inorganic acids may<br />

form salts on the surface that stop or slow<br />

further corrosion. Organic acids, particularly<br />

acetic acid, are the chief agents of deterioration<br />

in collections. Organic acid attack will<br />

produce fuzzy white deposits of lead formate<br />

(methanoate), lead acetate (ethanoate) and<br />

ultimately, lead carbonate. Whilst lead carbonate<br />

is considered stable under most circumstances,<br />

lead acetate and formate are not,<br />

because they may convert to lead carbonate.<br />

Care should be taken when removing these<br />

corrosion products, and in the disposal of both<br />

removed material and cleaning materials such<br />

as swabs, as they are a health hazard. Thickett<br />

et al. (1998) considered the risk posed to metal<br />

artefacts by carbonyl pollutants.<br />

Lead was often added to bronze casting<br />

alloys to improve the flow characteristics. Lead<br />

does not form an alloy with bronze, but segregates<br />

out as the metal cools. These lead<br />

pockets or inclusions can be preferentially<br />

attacked by organic acids under some display<br />

and storage conditions.<br />

Lead exposure in the workplace is subject<br />

to health and safety legislation. Protection<br />

measures against exposure are geared towards<br />

reducing escape of lead dust, fumes or vapour

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