78 DIY Science: Illustrated Guide to Home Chemistry Experiments
I wasn’t so lucky with another pipette, which was rated to deliver
43 drops/mL but in fact delivered closer to 44 drops/mL, at least
using my dropping technique. Still, once the actual delivery rate
is known, the nominal delivery rate is immaterial. Because I’ve
calibrated them, I can use those pipettes to deliver accurately
known small amounts of liquid reliably.
The number of drops per mL depends on the viscosity of the
liquid. For example, if you calibrate the number of drops per mL
using distilled water, that number is not valid for a more viscous
liquid such as olive oil or concentrated sulfuric acid, nor for a
less viscous liquid such as acetone or methanol. Fortunately,
the viscosity of the dilute aqueous solutions commonly used in
labs does not significantly differ from the viscosity of pure water.
UBISnG A URETTE
A burette is used to transfer solutions while measuring the
volume transferred with high accuracy. Although burettes are
sometimes used to measure and transfer nominal fixed volumes
(called aliquots) of a solution, for example, by transferring 5.0 mL
of a solution to each of several beakers that are to be used in a
subsequent procedure, that function is ordinarily better done using
a volumetric or Mohr pipette.
By far the most common use of a burette is for titration,
a procedure in which a solution (called the titrant) whose
concentration is known very accurately is dispensed by a burette
and reacted with a known volume of another solution of unknown
concentration (called the analyte). By measuring the amount of
titrant needed to neutralize the analyte, you can determine the
concentration of the analyte accurately.
Here is the proper way to use a burette:
- Rinse the inside of a clean burette thoroughly with the
solution it will contain. Allow the solution to run out
through the stopcock. Drain the burette completely.
Repeat the rinse at least once. - Make sure that the outside of the burette is clean and dry,
and then mount it securely to a laboratory stand using a
burette clamp of the proper size. - Fill the burette to above the zero mark, using a graduated
cylinder, small beaker, or other container. Use a funnel if
necessary to prevent spillage. - Run some solution through the stopcock to fill the burette
tip completely, making sure that there are no air bubbles
and that the level of the solution falls to or below the zero
mark. (It’s not necessary to hit the 0.00 mark exactly.) - Record the starting volume. When you complete the
titration, you’ll subtract this starting volume from the
final volume to determine the amount of solution you’ve
added. Read the value by placing your eye at the level of
the solution and reading the value at the bottom of the
meniscus, as shown in Figure 5-10 (which indicates a
reading of about 34.37 mL).
When you complete the titration, empty any remaining solution
into a waste container (using the proper disposal method for
NTE NdpoI vERSUS EqUIvALENCE poINT
The end point of a titration is the point at which the
titration is complete, typically when an added indicator
such as phenolphthalein changes color. (The end point
may also be determined by other methods, such as the
conductivity of the analyte reaching a minimum or the
pH of the analyte reaching 7.00.) The equivalence point
is closely related to but not necessarily identical with the
end point. The equivalence point is the point at which the
number of moles (or equivalents) of titrant exactly equals
the number of moles (or equivalents) of analyte.
Ideally, the end point should exactly equal the equivalence
point, but in the real world they are usually slightly
different. For example, you may titrate a hydrochloric
acid analyte with sodium hydroxide titrant, using
phenolphthalein as an indicator. Phenolphthalein is
colorless in acid solutions, and pink in base solutions, but
no color change occurs until the pH of the solution reaches
about 8.2, well into the basic range.
FIGURE 5-9: Calibrating a disposable pipette