December 26, 2024, 10:45:53 AM
Forum Rules: Read This Before Posting


Topic: Problems with calibration curve. Curve is not linear  (Read 3285 times)

0 Members and 1 Guest are viewing this topic.

Offline sprtfan

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Problems with calibration curve. Curve is not linear
« on: August 23, 2016, 12:38:13 PM »
I made a curve with concentrations at 0.05, 0.1, 0.5, 1, 5, 10, 15, 20 ng/ul in ethyl acetate.  I'm running the samples by GCMS.  I'm not sure the best was to describe the results but there is an obvious curve up starting with the 5 ng/ul standard and have an r^2 of 0.92.  If I break the standards up into groups, (0.05-1) and (5-20), I get an r^2 of 0.995 for both. 
I have made the standards 3 separate times and get the exact same results.  I did reuse my 1mg/ml stock solution each time though.  I use the 1 mg/ml stock to make the 5ng-20ng samples and then use the 5 ng sample to make the rest.  I'm using graduated disposable pipettes to make all of the dilutions.  I do not do this very often but have never had much trouble in the past.  I double checked my calculations and they should all be right.  Could the problem be with the ethyl acetate being volatile? Could I just be consistently making an error while making the dilutions?   Thanks for any insight

Offline Hunter2

  • Sr. Member
  • *****
  • Posts: 2314
  • Mole Snacks: +191/-50
  • Gender: Male
  • Vena Lausa moris pax drux bis totis
Re: Problems with calibration curve. Curve is not linear
« Reply #1 on: August 24, 2016, 08:23:47 AM »
Sometimes you have to use log(c), 1/log(c) and others if the normal values not linear. Which substance are u detecting.

Offline sprtfan

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Re: Problems with calibration curve. Curve is not linear
« Reply #2 on: August 24, 2016, 01:42:13 PM »
Sometimes you have to use log(c), 1/log(c) and others if the normal values not linear. Which substance are u detecting.

Thanks for the reply.  I figured out that the problem was caused by a background ion at a similar mass to the fragment that I was using that was disproportionately increasing the area counts of my lowest calibration points. 

Sponsored Links