The Natural History of ClaySearle, Alfred B. (Alfred Broadhead)
Science
The Natural History of Clay
Searle, Alfred B. (Alfred Broadhead)
Clay
Providing that wet clay is not heated to a temperature higher than that
of boiling water it appears to undergo no chemical change and on cooling
it will again take up water[15] and be restored to its original
condition except in so far as its colloidal nature may have been
affected by the heating. If, however, the temperature is raised to about
500° C. a decomposition of the material commences and water is evolved.
This water--which is commonly termed 'combined water'--is apparently an
essential part of the clay-molecule and when once it has been removed
the most important characteristics of the clay are destroyed and cannot
be restored. The reactions which occur when clay is heated are complex
and are rendered still more difficult to study by the apparent
polymerization of the alumina formed. Mellor and Holdcroft (29) have
recently investigated the heat reactions of the purest china clay
obtainable and confirm Le Chatelier's view (10) that on heating to
temperatures above 500° C. clay substance decomposes into free silica,
free alumina and water, the two former undergoing a partial
re-combination with formation of sillimanite (Al2O3SiO2) if a
temperature of 1200° C. is reached. Mellor and Holdcroft point out that
there is no critical point of decomposition for clay substance obtained
from china clay, as it appears to lose water at all temperatures, though
its decomposition proceeds at so slow a rate below 400° C. as to be
scarcely appreciable.
[Footnote 15: Some clays are highly hygroscopic and absorb moisture
readily from the atmosphere. According to Seger (7) this hygroscopicity
distinguishes true clay from silt and dust.]
After the whole of the 'combined water' has been driven off, if the
temperature continues to rise, it is found that at a temperature of 900°
C. an evolution of heat occurs. This exothermal point, together with the
endothermal one occurring at the temperature at which the decomposition
of the clay seems to be most rapid, has been found by Le Chatelier,
confirmed by Mellor and Holdcroft, to be characteristic of clay
substance derived from kaolin and china clay, and the two last-named
investigators state that it serves as a means of distinguishing
kaolinite or clayite from other alumino-silicates of similar
composition. These thermal reactions have not, as yet, been fully
studied in connection with plastic clays; with china clay, as already
noted, they probably indicate a polymerization of the alumina set free
by the decomposition of the clay substance, as pure alumina from a
variety of sources has been found by Mellor and Holdcroft to behave
similarly.
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