GC-FPD - peak in blank

Discussions about GC and other "gas phase" separation techniques.

3 posts Page 1 of 1
Hi,

I am running samples on GC-FPD.

My calibration and sample peaks were all tailing so I was suggested to cut the end of the column from the detector and increase the carrier flow rate.

As I was cutting the column I noticed the detector inlet was not in the correct amount so I adjusted for that as well.

After cutting I ran my blank and did a bakeout. I have a total of 3 chromatographs (after column cut) and they all have an unidentified peak that was not present before.

Any suggestions on what I should do next?
I would think it is more on the inlet side of the column. Usually such problems come from high boiling point organics or inorganic materials accumulating in the inlet and the front end of the column, not so much the detector end.

Have you changed injection port liner or remove a few centimeters from the inlet end of the column?
The past is there to guide us into the future, not to dwell in.
Three questions. 1) Sulfur or phosphorous mode? 2) Peak with no injection, just an oven run? 3) Sharp peak, ugly broad peak, what kind of peak?

Best regards,

AICMM
3 posts Page 1 of 1

Who is online

In total there is 1 user online :: 0 registered, 0 hidden and 1 guest (based on users active over the past 5 minutes)
Most users ever online was 1117 on Mon Jan 31, 2022 2:50 pm

Users browsing this forum: No registered users and 1 guest

Latest Blog Posts from Separation Science

Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry