Archive for the ‘Optimizing Applications’ Category

One Stop Shop for Essential Oils Chromatograms

In the past few months, we have collected a variety of chromatograms using two different column phases, and three different column dimension formats. The peak identifications were performed using some standards but mostly from the NIST MS EI spectra library, 2005 edition. Let us know what you think in the comments below. Citronella Java GC_FF1296 […]

Discovering Analyte Breakdown On-Column

I completed my winter internship at Restek and my main task was to expand the Pro-EZGC libraries. So I created a library for Nitrosamines on the Rxi-1301Sil MS and while acquiring data we noticed a foot on a couple of my peaks. I attempted to translate the simulation to a column with the same phase, […]

Pro EZGC Update: Comprehensive 209 compound Library of Brominated Diphenyl Ethers and a New Column Format

While attending Dioxin 2018 in Krakow, I noticed that several academic researchers were studying  the toxicity of specific PBDE congeners not on the standard target compound list for EPA method 1614 (or the EU equivalent). Though PBDE mixtures have been phased out of production and use, the concentrations in the environment have not been declining […]

GC Inlet Liner Selection, Part IV: Liner Volume and Diameter

In parts I and II of this blog series I discussed the various liner configurations available for both split and splitless analyses.  One thing I did not mention was liner volume and inner diameter.  Most of the liners I compared are available in multiple inner diameters.  For the comparisons I did, I used a 4 […]

A closer look at selectivity and tailing: Essential oils and Wax phases

The most common way to analyze essential oils is to use GC with either a FID or MS. The wax-based columns are the number one choice for many users and following up on an excellent blog post by Corby, I wanted to evaluate two wax in Restek inventory: Stabilwax and Rtx-Wax. The essential oil we chose was […]

What impurities are hiding in your monocyclic aromatic solvents?

As we approach the end of the year we are indulging in a bit of nostalgia and most experts agree that reminiscing about the past is a good thing1. It makes us more optimistic and generous. Researchers also noticed that in cold rooms we are more inclined to nostalgize than if we are in a […]

GC Inlet Liner Selection, Part III: Inertness

The inlet liner is the first surface analytes will interact with after introduction into a GC.  It is critical that liners are deactivated, as a number of adverse interactions can occur between analytes and the glass surface.  Deactivations typically involve some type of silanization of the surface to cover active sites inherent in glass, such […]

Amines: Topaz or Base Deactivated Liners?

Amines can be difficult to analyze by GC, since they are active and adsorb to surfaces within the chromatographic system, including the inlet liner and the column.  This leads to loss of compound response, and peak tailing.  While deactivations can help to mitigate these effects, the quality of deactivations varies.  Primary amines are especially difficult, […]

GC Inlet Liner Selection, Part IIB: Split Liners Continued

My colleague, Alan Sensue, asked a couple of great questions in regards to my previous blog post on split liners.  To summarize, he was interested in what happens to responses for the various liners when you change split ratios.  For instance, if you go from a 20:1 split to a 40:1 split, do detected peak […]

GC Inlet Liner Selection, Part II: Split Liners

In the previous installment of this blog series, I discussed liner selection for splitless analyses (GC Inlet Liner Selection, Part I: Splitless Liner Selection).  Today I’d like to discuss liners for split analyses.  During a split injection, the split vent is open and the majority of the flow is vented.  The split ratio, set by […]