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

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82 ENAMELS AND ENAMELLING.<br />

under examination is fit for our purposes or not. In <strong>the</strong><br />

enamel mass m<strong>an</strong>g<strong>an</strong>ese is converted in<strong>to</strong> silicate, <strong><strong>an</strong>d</strong> as a<br />

rule <strong>the</strong> small qu<strong>an</strong>tity of m<strong>an</strong>g<strong>an</strong>ese present in potash does<br />

not affect <strong>the</strong> properties of <strong>the</strong> enamel.<br />

The alkaline earths lime, chalk, gypsum, dolomite, argil-<br />

laceous limes<strong>to</strong>ne, barytes, wi<strong>the</strong>rite,<br />

etc. are examined in <strong>the</strong><br />

same m<strong>an</strong>ner, by heating in <strong>the</strong> reducing flame <strong><strong>an</strong>d</strong> noting<br />

<strong>the</strong> colour. As, however, m<strong>an</strong>y<br />

of <strong>the</strong>se subst<strong>an</strong>ces are in-<br />

fusible before <strong>the</strong> blowpipe, recourse is had <strong>to</strong> <strong>an</strong>hydrous<br />

borax in order <strong>to</strong> obtain tr<strong>an</strong>sparent samples.<br />

When carbonates are fused along with borax, <strong>the</strong> bead is<br />

at first turbid from <strong>the</strong> accomp<strong>an</strong>ying bubbles of carbon<br />

dioxide liberated by <strong>the</strong> boric acid ; in such event <strong>the</strong> bead<br />

must be maintained in a state of fusion until all <strong>the</strong> gas has<br />

O<br />

escaped <strong><strong>an</strong>d</strong> <strong>the</strong> mass becomes quite clear.<br />

The enamel fluxes borax, boric acid, fluor spar <strong><strong>an</strong>d</strong> cullet<br />

may all be tested for iron in <strong>the</strong> above m<strong>an</strong>ner, all that is<br />

usually necessary being <strong>to</strong> fuse <strong>the</strong>m, without admixture, <strong><strong>an</strong>d</strong><br />

examine <strong>the</strong>ir behaviour alternately in <strong>the</strong> reducing <strong><strong>an</strong>d</strong><br />

oxidising flames.<br />

Testing Silica.<br />

This subst<strong>an</strong>ce, in <strong>the</strong> state of quartz meal <strong><strong>an</strong>d</strong> s<strong><strong>an</strong>d</strong>, is<br />

quite infusible by itself, <strong><strong>an</strong>d</strong> consequently has <strong>to</strong> be fused<br />

with <strong>an</strong> alkali, when tested for impurities, ordinary soda (of<br />

course free from iron) being generally employed on account<br />

of <strong>the</strong> fusibility of its bead. The mixture must be heated<br />

until all <strong>the</strong> carbon dioxide has been driven off, leaving <strong>the</strong><br />

bead quite clear.<br />

If <strong>the</strong> test fail <strong>to</strong> reveal iron in <strong>the</strong> silica or o<strong>the</strong>r sub-<br />

st<strong>an</strong>ce under examination, but leaves <strong>the</strong> bead grey, yellow,<br />

or brownish after heating in <strong>the</strong> reduction flame, this colora-<br />

tion may be due <strong>to</strong> <strong>the</strong> presence of finely divided carbon.<br />

This mav be readily confirmed by reheating <strong>the</strong> bead with <strong>an</strong>

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