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Improvement signal to noise ratio
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
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How can I improve the signal to noise ration for UV detector in HPLC system?
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- tom jupille
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Two ways: more signal, or less noise
More signal:
- inject a bigger sample
- use a stronger mobile phase to get your peaks of interest earlier (narrower) in the chromatogram (isocratic)
- use a steeper gradient to make your peaks narrower
- make sure you detect at an absorbance maximum wavelength for your analyte
- use a smaller column diameter (less dilution of the sample during chromatography)
- get a column of higher efficiency (plate number) to give you narrower peaks.
Less noise:
- if your lamp is old, replace it
- make sure your lamp is properly aligned
- make sure your detector cell is clean. Check the cell windows; if they have "solarized", replace them
- make sure your mobile phase is well degassed
- if you are working at short wavelength (near the UV cutoff of your mobile phase), make sure you are using high-purity solvents
- if you are running a gradient, do the "three-blank-gradient" test to find out if contaminated "A" solvent is contributing garbage peaks.
- Re-run the manufacturer's recommended performance qualification test to verify that the detector is, in fact, operating to its specifications.
More signal:
- inject a bigger sample
- use a stronger mobile phase to get your peaks of interest earlier (narrower) in the chromatogram (isocratic)
- use a steeper gradient to make your peaks narrower
- make sure you detect at an absorbance maximum wavelength for your analyte
- use a smaller column diameter (less dilution of the sample during chromatography)
- get a column of higher efficiency (plate number) to give you narrower peaks.
Less noise:
- if your lamp is old, replace it
- make sure your lamp is properly aligned
- make sure your detector cell is clean. Check the cell windows; if they have "solarized", replace them
- make sure your mobile phase is well degassed
- if you are working at short wavelength (near the UV cutoff of your mobile phase), make sure you are using high-purity solvents
- if you are running a gradient, do the "three-blank-gradient" test to find out if contaminated "A" solvent is contributing garbage peaks.
- Re-run the manufacturer's recommended performance qualification test to verify that the detector is, in fact, operating to its specifications.
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
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- Posts: 418
- Joined: Mon Aug 15, 2005 3:06 pm
One more: Reduce your dead volume as much as is practical.
Easy and cheap: Minimize the length and diameter of the tubing from the end of your column to your detector.
Less easy, still pretty cheap: Re-plumb your system with narrower bore tubing and be absolutely positive you don't have any leaks. Also make sure that all of your compression fittings are properly made - no ferrules way out at the end of the tubing. Remove any unnecessary unions, too; I've seen patches in the strangest places.
Cheers!
Easy and cheap: Minimize the length and diameter of the tubing from the end of your column to your detector.
Less easy, still pretty cheap: Re-plumb your system with narrower bore tubing and be absolutely positive you don't have any leaks. Also make sure that all of your compression fittings are properly made - no ferrules way out at the end of the tubing. Remove any unnecessary unions, too; I've seen patches in the strangest places.
Cheers!
http://the-ghetto-chromatographer.blogspot.com/
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