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Purpose:
Test and analyze outdoor water
samples around the Harper campus
to determine if the levels of
permissibility of the anions meet
the criteria of the EPA.
Ion Chromatography
A sample is injected into the
instrument and goes through a
column. When the sample is in the
column, the ions are separated. Ion
concentration is then measured
through electric conductivity.
Instrument Calibration
The Ion Chromatograph is calibrated by
generating calibration curves for the anions of
interest. Ions are then identified by the time it
takes the ion to get to a detector within the
machine. Methods were generated so that
each ion had a different retention time. For
the Ion Chromatograph, the concentration of
an ion is proportional to the conductivity of
the ions in the solution. The standardized
solutions of the four anions made were used
to create graphs of concentration vs.
conductivity. From these graphs, best fit
equations were obtained to allow us to
calculate the concentration of an ion, given
the conductivity. The calibration was checked
several times throughout the year.
Identification of Anions
0.5g of four different substances were combined with 100mL of water
(H2O) to form four different compounds of stock standard solutions.
These substances were sodium sulfate (NaSO4
2-), sodium chloride
(NaCl-), sodium nitrate (NaNO3
-), and sodium fluoride (NaF-). After,
2mL, 3mL, 5mL, and 10mL of each solution were extracted from the
compounds and placed into 100mL volumetric flasks. Then, 3 vials of
each concentration of each compound will be filled, coming to a total
of 72 vials. Lastly, all 72 vials ran through the machine along with 2
blanks at the beginning and end of the sequence. Blanks are vials filled
with ultra pure deionized water used to detect any abnormalities
within the machine.
Retrieval and Preparation of Outdoor Samples
Using rubber gloves and bottles, we took our water
samples. At the sample site, we filled and emptied the
bottle three times. By doing so, we ensured that the
sample was not contaminated from previous samples taken
using the same bottle. After being acquired, samples were
allowed to settle for about three days. This helped to
prevent any materials found in the samples from blocking
the flow of the Ion Chromatography machine. Then, two
vials of each sample were prepared, coming to a total of 28
vials including the 4 blanks.
Anions Analyzed
Sulfate (SO4
2-), Chloride
(Cl-), Nitrate (NO3
-),
Fluoride (F-)
References
EPA. "Title 35: Environmental Protection Subtitle C: Water
Pollution Chapter I: Pollution Control Board." EPA. EPA, 28 Jan.
2008. Web. 2 May 2011.
<http://www.epa.gov/waterscience/standards/wqslibrary/il/il_5_c
302.pdf>.
Google. Photograph. Palatine. Google. Google. Web. 2 May 2011.
<http://maps.google.com/maps?hl=en&tab=wl>.
National standards
Sulfate 240 mg/L
Chloride 250 mg/L
Nitrate 10 mg/L
Fluoride 15 mg/L
Analysis of Water Using Ion Chromatography
Brittany Bochenko, Ivan Rojas
Dr. Thomas Dowd
Department of Chemistry, Harper College Palatine, IL 60067

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AnalysisofWaterUsingIonChromatographyFINAL-2

  • 1. Purpose: Test and analyze outdoor water samples around the Harper campus to determine if the levels of permissibility of the anions meet the criteria of the EPA. Ion Chromatography A sample is injected into the instrument and goes through a column. When the sample is in the column, the ions are separated. Ion concentration is then measured through electric conductivity. Instrument Calibration The Ion Chromatograph is calibrated by generating calibration curves for the anions of interest. Ions are then identified by the time it takes the ion to get to a detector within the machine. Methods were generated so that each ion had a different retention time. For the Ion Chromatograph, the concentration of an ion is proportional to the conductivity of the ions in the solution. The standardized solutions of the four anions made were used to create graphs of concentration vs. conductivity. From these graphs, best fit equations were obtained to allow us to calculate the concentration of an ion, given the conductivity. The calibration was checked several times throughout the year. Identification of Anions 0.5g of four different substances were combined with 100mL of water (H2O) to form four different compounds of stock standard solutions. These substances were sodium sulfate (NaSO4 2-), sodium chloride (NaCl-), sodium nitrate (NaNO3 -), and sodium fluoride (NaF-). After, 2mL, 3mL, 5mL, and 10mL of each solution were extracted from the compounds and placed into 100mL volumetric flasks. Then, 3 vials of each concentration of each compound will be filled, coming to a total of 72 vials. Lastly, all 72 vials ran through the machine along with 2 blanks at the beginning and end of the sequence. Blanks are vials filled with ultra pure deionized water used to detect any abnormalities within the machine. Retrieval and Preparation of Outdoor Samples Using rubber gloves and bottles, we took our water samples. At the sample site, we filled and emptied the bottle three times. By doing so, we ensured that the sample was not contaminated from previous samples taken using the same bottle. After being acquired, samples were allowed to settle for about three days. This helped to prevent any materials found in the samples from blocking the flow of the Ion Chromatography machine. Then, two vials of each sample were prepared, coming to a total of 28 vials including the 4 blanks. Anions Analyzed Sulfate (SO4 2-), Chloride (Cl-), Nitrate (NO3 -), Fluoride (F-) References EPA. "Title 35: Environmental Protection Subtitle C: Water Pollution Chapter I: Pollution Control Board." EPA. EPA, 28 Jan. 2008. Web. 2 May 2011. <http://www.epa.gov/waterscience/standards/wqslibrary/il/il_5_c 302.pdf>. Google. Photograph. Palatine. Google. Google. Web. 2 May 2011. <http://maps.google.com/maps?hl=en&tab=wl>. National standards Sulfate 240 mg/L Chloride 250 mg/L Nitrate 10 mg/L Fluoride 15 mg/L Analysis of Water Using Ion Chromatography Brittany Bochenko, Ivan Rojas Dr. Thomas Dowd Department of Chemistry, Harper College Palatine, IL 60067