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Back Test for Sodium Sulfite | Up Utilitiesman Basic Volume 02 - Manual for electric, plumbing, water and other utilities | Next Test for Total Dissolved Solids |
4. Bring the water in the 150-ml beaker to a boil by
any convenient method.
5. Remove the source of heat and immediately
pour the starch paste into the boiling water while stirring
the solution.
6. Put a crystal of thymol into the starch solution
and stir. After the solution has cooled, pour off any
scum on the surface and transfer 30 ml to the
indicator-dropping bottle.
7. The starch solution loses its sensitivity as an
indicator after a time. Addition of the thymol preserves
it for about 2 weeks. The starch should be dated when
prepared.
In making the sodium sulfite test, proceed as
follows:
1. Transfer 1 ml of hydrochloric acid 3N to a clean,
marked test tube by measuring out 0.5-ml portions with
the dropper of the acid-dropping bottle.
2. From the starch-dropping bottle, transfer 0.5 ml
of starch to the marked test tube.
3. Without disturbing any settled sludge in the
sample, pour enough of the sample into the marked test
tube to bring the level up to the first mark (25-ml). Stir
the mixture in the tube with the plunger end of the
stirring rod.
4. To add the standard potassium iodate-iodide
reagent to the mixture in the marked test tube, have the
marked test tube supported and the stirring rod placed in
the tube, so the reagent can be added with one hand
while the mixture is stirred with the other. Fill the
8-inch dropper with standard potassium iodate-iodide
reagent from the stock bottle by sucking it up with the
rubber bulb. (The dropper must be kept clean and
reserved for this test only.)
5. Add the reagent to the mixture in the marked test
tube, one drop at a time, counting the number of drops
and stirring after each is added until a permanent blue
color, which is not removed by stirring, is obtained. The
standard iodate-iodide reagent reacts with sodium
sulfite in the mixture, and the formation of the
permanent blue color from the action of excess reagent
with the starch shows that the iodate-iodide reagent has
consumed all the sodium sulfite in the mixture.
6. Each drop of iodate-iodide reagent used (except
the last one) indicates 5 ppm of sodium sulfite in the
boiler water sample. To figure the concentration of
sodium sulfite in the boiler water, multiply the total
number of drops of the standard iodate-iodide reagent
used, less one, by 5. For example, when 5 drops were
used, subtract 1 from 5 = 4, 5 x 4 = 20 ppm.
7. Record the results of the test as ppm.
Test for pH
The value of pH indicates the degree of acidity or
alkalinity of a sample. A pH of 7.0 represents the
neutral point; the lesser values denote acidity; the
greater values denote alkalinity. The test is made as
soon as possible after you take the sample. Avoid
exposure to the air as much as possible to reduce
absorption of CO2.
The following equipment is used in making the pH
test of boiler water:
One 2-oz bottle
One 50-ml beaker
Two vials of indicator paper, hydrions C pH 11
to 12
Two vials of indicator paper, hydrions pH 10 to
20
In conducting the test for pH of boiler water,
remove a strip of pH 10 to 12 indicator paper from the
vial and dip it into the sample in the beaker. Keep the
paper immersed for 30 seconds; then remove it. When
the sample does not change the color of the paper or
colors it yellow or light orange, the pH of the sample is
too low and the test is finished. When the paper turns
orange or red, the pH is either satisfactory or too high.
In that case, remove a strip of paper of pH 11 to 12
from the vial and dip it into the sample in the beaker.
Keep the paper immersed for 30 seconds; then remove
it. When the sample does not change the color of the
paper or colors it a light blue, the pH is satisfactory.
When the paper turns deep blue, the pH is higher than
necessary. Blow down or reduce the dosage of caustic
soda (NaOH).
Test for pH of Treated
Condensate
In making a test for pH of treated condensate, take
the sample from a point in the return piping near which
condensation takes place, such as after a trap, or
preferably where the return-line corrosion is known to
occur. The sample must represent water flowing in the
return lines.
Water taken from the return tank,
especially of large installations, generally shows a
higher pH. A sample should not be taken from a
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