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Enamels and enamelling; an introduction to the preparation and ...

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120 ENAMELS AND ENAMELLING.<br />

such event it is easy <strong>to</strong> increase <strong>the</strong> fusibility of <strong>the</strong> product<br />

by <strong>the</strong> aid of borax.<br />

The effect of magnesia is <strong>to</strong> render <strong>the</strong> enamel more readily<br />

distributable over <strong>the</strong> surface <strong>to</strong> which it is applied, <strong><strong>an</strong>d</strong> <strong>the</strong><br />

use of this subst<strong>an</strong>ce is <strong>the</strong>refore particularly advisable when<br />

preparing enamels desired <strong>to</strong> distribute uniformly<br />

on small<br />

articles.<br />

A very import<strong>an</strong>t point in <strong>the</strong> <strong>preparation</strong> of all enamels<br />

is <strong>the</strong> so-called decoloration by me<strong>an</strong>s of oxidising bodies,<br />

added in order <strong>to</strong> convert ferrous oxide in<strong>to</strong> ferric oxide, <strong><strong>an</strong>d</strong><br />

<strong>the</strong>reby diminish <strong>the</strong> pigmentary power exerted by <strong>the</strong><br />

former. It is evident that <strong>the</strong> sole object accomplished by<br />

this treatment is <strong>the</strong> production of enamels with a yellow<br />

tinge, but not perfectly colourless, <strong>the</strong> sole me<strong>an</strong>s of effecting<br />

this latter desideratum being <strong>the</strong> use of perfectly pure, <strong><strong>an</strong>d</strong><br />

<strong>the</strong>refore costly, raw materials.<br />

There is, however, a simple me<strong>an</strong>s whereby enamel masses<br />

from somewhat impure materials c<strong>an</strong> be obtained of a fine<br />

white colour, <strong><strong>an</strong>d</strong> this is by <strong>the</strong> addition of very small qu<strong>an</strong>ti-<br />

ties of fine smalt <strong>to</strong> <strong>the</strong> mass. Like all cobalt <strong>preparation</strong>s,<br />

smalt is capable of imparting a deep blue colour <strong>to</strong> glass, but<br />

<strong>the</strong> shade in this case is complementary <strong>to</strong> <strong>the</strong> yellow tinge<br />

produced by ferric oxide, <strong><strong>an</strong>d</strong> <strong>the</strong>refore <strong>the</strong> one counteracts<br />

<strong>the</strong> o<strong>the</strong>r, <strong>the</strong> result being <strong>to</strong> leave <strong>the</strong> enamel quite white.<br />

Of course this mutual destruction of colour only occurs<br />

when <strong>the</strong> right proportion of <strong>the</strong> two pigmentary bodies is hit<br />

upon ;<br />

for if <strong>an</strong> insufficient amount of smalt be taken, <strong>the</strong><br />

yellow from <strong>the</strong> iron is only<br />

weakened <strong><strong>an</strong>d</strong> still remains<br />

apparent, whilst <strong>an</strong> excess of smalt imparts a bluish (milkwhite)<br />

tinge <strong>to</strong> <strong>the</strong> mass.<br />

The expense of decolorising enamels in this way is a<br />

negligible fac<strong>to</strong>r a minute qu<strong>an</strong>tity of smalt sufficing for a<br />

large batch of enamel mass. All that is necessary<br />

is <strong>to</strong><br />

accurately determine, by several tentative experiments, how

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