Nitrate nitrogen in water is determined by reacting with phenoldisulfonic acid
to give a yellow color with an absorption maximum at \(410 \mathrm{nm}\). A 100
-mL sample that has been stabilized by adding \(0.8 \mathrm{~mL} \mathrm{H}_{2}
\mathrm{SO}_{4} / \mathrm{L}\) is treated with silver sulfate to precipitate
chloride ion, which interferes. The precipitate is filtered and washed
(washings added to filtered sample). The sample solution is adjusted to
\(\mathrm{pH} 7\) with dilute \(\mathrm{NaOH}\) and evaporated just to dryness.
The residue is treated with \(2.0 \mathrm{~mL}\) phenol disulfonic acid solution
and heated in a hot-water bath to aid dissolution. Twenty milliliters
distilled water and \(6 \mathrm{~mL}\) ammonia are added to develop the maximum
color, and the clear solution is transferred to a 50 -mL volumetric flask and
diluted to volume with distilled water. A blank is prepared using the same
volume of reagents, starting with the disulfonic acid step. A standard nitrate
solution is prepared by dissolving \(0.722 \mathrm{~g}\) anhydrous
\(\mathrm{KNO}_{3}\) and diluting to 1 L. A standard addition calibration is
performed by spiking a separate 100 -mL portion of sample with \(1.00
\mathrm{~mL}\) of the standard solution and carrying through the entire
procedure. The following absorbance readings were obtained: blank, 0.032 ;
sample, 0.270 ; sample plus standard, 0.854 . What is the concentration of
nitrate nitrogen in the sample in parts per million?