Archive for the ‘Food’ Category

Pesticides are like Siblings – some get along well and some don’t – No. . .Really?

My colleague, Joe Konschnik and I have been asked by many food chemists out there about how much they can trust their pesticides mixes after they combine them into one single larger mixture for calibrating their instrument, or monitoring the accuracy and precision of their method – and rightfully so.  Well, like siblings, sometimes they […]

What dSPE works with spinach in GC-MS/MS analysis? #NationalSpinachDay

Today is a National Spinach Day! What is a better way to celebrate than to talk about spinach analysis? During part 1 of my blog series, I discussed what dSPE was best for celery. I found that most dSPE, with the exception of dSPE containing high amounts of graphitized carbon black (GBC), showed acceptable analyte recovery […]

Choosing the right dispersive SPE for GC-MS/MS analysis of celery

I’ve recently started experimenting with QuEChERS extractions for pesticide analysis. The available options are overwhelming, especially when it comes to dispersive solid phase extraction (dSPE) for the cleanup. For starters, I’ve been looking at the smaller volume dSPE (2 mL, summarized in Table 1), because I didn’t want to waste the raw material, solvents and […]

Trade in Splitless for Split: Faster Speed & More Miles Analyzing 3-MCPD / Glycidyl esters

In my recent work with analysis of 3-MCPD and glycidyl esters, I reviewed the available methods by AOCS and they list splitless or pulsed splitless injection. Splitless injection theoretically transfers all of the sample onto the column, allowing the analyst to achieve trace levels of detection. However, there are limitations. Both splitless hold-time and focusing […]

FAMEs blog part 4: Struggling with using hydrogen for AOCS methods Ce 1j-07 or Ce 1h-05?

This blog a part of a series: part 1, part 2, and part 3 Recently I came across customers’ issue with AOCS method Ce 1h-05 used with hydrogen as a carrier gas and I’ve decided to look more closely into what conditions are suggested for this analysis. While at it, I looked also into conditions of methods […]

FAMEs blog part 3: If I Use a Rt-2560 with my GC-MS will it explode?

This blog a part of a series: part 1, part 2, and part 4 Disclaimer: Do not use non-bonded columns, such as Rt-2560, in GC-MS for routine analysis! If you have the need to run some samples, here is what to expect (i.e. quite a bit of bleed) In my last blog, I talked about how […]

Trans fatty acids analysis part 2: Let’s look at actual samples with incurred TFAs

This blog a part of a series: part 1, part 3, and part 4 In my previous blog, I’ve tried and failed to acquire a sample that contained any trans fatty acids (TFAs). While this is a great news for everyone’s health, the scientist in me was somewhat disappointed. That’s why I first decided to cheat […]

The usage of Reference Standards in MOSH/MOAH Analysis

Abstract The unintended migration of mineral oil compounds into food, e.g from packing materials or from production processes are a raising topic in industry and scientific discussions. For a first screening, an LC-GC/FID method was established in the last years. In collaboration with Axel Semrau, Restek has developed ready to use standards for quantification and […]

The main source of artificial trans fatty acids is banned on June 18, 2018. Are we ready?

This blog a part of a series: part 2, part 3, and part 4 One of the leading causes of deaths in the world is heart disease, accounting for approximately 24% of deaths in the USA in 2015.1 One of the factors linked to cardiovascular diseases is consumption of artificial trans fatty acids (TFAs). Artificial TFAs are […]

Stabilwax Pro-EZGC Library Updated

Recently I blogged about the expansion of Rxi-624 EZGC library, this time I want to focus on an update of Stabilwax. At 462 compounds, this library covers the most searched, such as methanol or xylenes, and requested compounds, such as acetic and formic acid.* Similar to my last blog, I’d like to show you a […]