A text-book of assaying : $b for the use of those connected with mines.Beringer, C. (Cornelius)
Science
A text-book of assaying : $b for the use of those connected with mines.
Beringer, C. (Cornelius)
Assaying
Sometimes it is necessary to draw up a table which will show, without
calculation, the weight of substance equivalent to a given volume of gas
or of solution. The substance used for standardising should be, whenever
possible, a pure sample of the substance to be determined--that is, for
copper assays pure copper should be used, for iron assays pure iron, and
so on; but when this cannot be got an impure substance may be used,
provided it contains a known percentage of the metal, and that the
impurities present are not such as will interfere with the accuracy of
the assay. Including compounds with these, the standard may be
calculated by multiplying the standard got in the usual way, by the
percentage of metal in the compound or impure substance, and dividing by
100. If, for example, the standard 1.008 gram was obtained by using a
sample of iron containing 99.7 per cent. of metal, the corrected
standard would be 1.008×99.7/100 = 1.005.
In volumetric analysis the change brought about must be one in which the
end of the reaction is rendered prominent either by a change of colour
or by the presence or absence of a precipitate. If the end of the
reaction or finishing-point is not of itself visible, then it must be
rendered visible by the use of a third reagent called an indicator.
For example, the action of sulphuric acid upon soda results in nothing
which makes the action conspicuous; if, however, litmus or
phenolphthalein be added the change from blue to red in the first case,
or from red to colourless in the second, renders the finishing-point
evident. Some indicators cannot be added to the assay solution without
spoiling the result; in which case portions of the assay solution must
be withdrawn from time to time and tested. This withdrawal of portions
of the assay solution, if rashly done, must result in loss; if, however,
the solution is not concentrated, and if the portions are only withdrawn
towards the end of the titration, the loss is very trifling, and will
not show-up on the result. The usual plan adopted is to have a solution
of the indicator placed in drops at fairly equal intervals distributed
over a clean and dry white porcelain-plate: a drop or two of the
solution to be tested is then brought in contact with one of these and
the effect noted. Another plan is to have thin blotting-paper, moistened
with a solution of the indicator and dried; a drop of the solution to be
tested placed on this shows the characteristic change. When the assay
solution contains a suspended solid which interferes with the test, a
prepared paper covered with an ordinary filter-paper answers very well;
a drop of the solution to be tested is placed on the filter-paper, and,
sinking through, shows its effect on the paper below.
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account