Advertisement

Surrogate Recovery Calculation

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

2 posts Page 1 of 1
I am trying to figure out how to calculate "surrogate recovery" for EPA 552.3 (haloacetic acids). The method uses an internal standard AND a surrogate (2-bromobutyric acid). The surrogate should tell us how efficient the extraction and methylation steps are. The EPA method, in Sect. 9.7, gives the formula R = (A/B) x 100%, where A = "calculated surrogate concentration for the Field Sample" and B = "fortified concentration of the surrogate". It seems to me that any % recovery boils down to "what you actually got" divided by "what you should have got", times 100. So the A term would be the area of the surrogate peak I actually got on a sample injection, and the B term would be the area of a completely extracted, completely methylated sample of 2-bromobutyric acid. But the EPA method does not explicitly mention or describe running a premethylated sample.
Am I missing something here? Thanks in advance for any comments!

PS. I love this website! This is my first post.
I am trying to figure out how to calculate "surrogate recovery" for EPA 552.3 (haloacetic acids). The method uses an internal standard AND a surrogate (2-bromobutyric acid). The surrogate should tell us how efficient the extraction and methylation steps are. The EPA method, in Sect. 9.7, gives the formula R = (A/B) x 100%, where A = "calculated surrogate concentration for the Field Sample" and B = "fortified concentration of the surrogate". It seems to me that any % recovery boils down to "what you actually got" divided by "what you should have got", times 100. So the A term would be the area of the surrogate peak I actually got on a sample injection, and the B term would be the area of a completely extracted, completely methylated sample of 2-bromobutyric acid. But the EPA method does not explicitly mention or describe running a premethylated sample.
Am I missing something here? Thanks in advance for any comments!

PS. I love this website! This is my first post.
A should be the actual recovery concentration not peak area, the value obtained when comparing the sample to an appropriate standard and B is the theoretical 100% recovery.
So if you spiked at 5ug/ml and recovered 4.1ug/ml you would have an 82% surrogate recovery.
2 posts Page 1 of 1

Who is online

In total there are 79 users online :: 1 registered, 0 hidden and 78 guests (based on users active over the past 5 minutes)
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am

Users browsing this forum: Google Adsense [Bot] and 78 guests

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