Can I Create a Calibration Curve Using Only Peak Area Data?

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A calibration curve can be created using peak area data from an ion chromatography experiment by establishing two points: one at 0 ppm concentration (zero peak area) and another at 10 ppm concentration (known peak area). This allows for a linear relationship to be plotted. While using peak height is also a viable option, the discussion emphasizes using peak area as instructed. Once the calibration curve is established, unknown concentrations can be determined by solving for x using the known area and gradient. Normalizing the data is suggested, but the primary focus should remain on using peak area for accuracy.
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I've just done an ion chromatography experiment and have normalized my data for a known sample which has a known concentration of 10ppm.

I know that the first large peak is due to F- ions and so the area of the peak is propositional to the concentration of the ion.

Given that I know the area, how can I get the calibration curve just by this information ?
 
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Assume signal would be zero if there were no F- at all, that gives you two pints, enough to draw a straight line.

That's not the best approach in general, but better than nothing.
 
Borek said:
Assume signal would be zero if there were no F- at all, that gives you two pints, enough to draw a straight line.

That's not the best approach in general, but better than nothing.
Thanks, but I'm not sure I fully understand.

This is my current data graph; https://i.gyazo.com/72d8f842cc504e924d1d0f106fb0266a.png
The first large peak corresponds to F- ions.
If I assumed the signal as 0 how would I plot a calibration curve ? Would it be possible for me to choose 2 points on the curve which produce a linear relationship ?Thank you in advance for your help :)
 
You know the area of a peak that correspond to a 10 ppm concentration, yes?

Assume 0 ppm would produce no peak - or a peak of area 0.

That gives you two points for calibration curve - one for 0 ppm concentration and one for 10 ppm concentration.
 
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Borek said:
You know the area of a peak that correspond to a 10 ppm concentration, yes?

Assume 0 ppm would produce no peak - or a peak of area 0.

That gives you two points for calibration curve - one for 0 ppm concentration and one for 10 ppm concentration.
I see, thanks.

To calculate the area, can I normalise my data so that the area under the curve is directly po
Borek said:
You know the area of a peak that correspond to a 10 ppm concentration, yes?

Assume 0 ppm would produce no peak - or a peak of area 0.

That gives you two points for calibration curve - one for 0 ppm concentration and one for 10 ppm concentration.
Thanks. I've managed to do it and used excel to calculate the gradient, in the form y=mx+c
One last question.

If I run a sample with an unknown concentration of F-, if I know the area under the curve (y) and the gradient (m), knowing that c=0, would I just solve for (x) which would be my concentration of F- in the unknown sample ?
 
CannonSLX said:
To calculate the area, can I normalise my data so that the area under the curve is directly po

You lost something here. You can use peak height instead of the area, typically these are related (and in the case of a nice curve - like the one you have - it is quite good approach).

CannonSLX said:
If I run a sample with an unknown concentration of F-, if I know the area under the curve (y) and the gradient (m), knowing that c=0, would I just solve for (x) which would be my concentration of F- in the unknown sample ?

Yes.
 
Borek said:
You lost something here. You can use peak height instead of the area, typically these are related (and in the case of a nice curve - like the one you have - it is quite good approach).
Yes.
We've been told to use area, so would normalising be the right idea for this approach ?
 
If you are told to use area - use area.
 
Borek said:
If you are told to use area - use area.
Thanks for your help :)
 
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