Achieving the Lowest Limits of Identification – GC-MS with Cold EI versus Standard EI with High Efficiency Source

Aviv Amirav, Tel Aviv University and Aviv Analytical Ltd.

Executive Summary  

GC-MS sensitivities are specified with octafluoronaphthalene (OFN). However, for many GC-MS users the most important operational parameter is the sample limits of identification. We compared the Aviv Analytical GC-MS with Cold EI with the Agilent 5977B GC-MS with high efficiency ion source (HES) in sample identification. We found that Cold EI far outperforms the 5977B-HES in both detection and identification limits. Cold EI detected and identified thirteen impurity compounds in a given test mixture while the HES standard EI failed to detect most of these impurities and failed to identify any of them. In this article we demonstrate and discuss several Cold EI benefits of superior sensitivity, better identification capability, greater range of compounds amenable for analysis and faster speed of analysis. The graphical abstract figure above demonstrates the absence of impurity peaks in the TIC with HES versus at least thirteen detected peaks in Cold EI in which each peak exhibits a molecular ion and is amenable for trustworthy identification.   

Permethrin Drug Impurity Analysis with GC-MS with Cold EI and the Road to Failure in Such Analysis by GC-MS with Standard EI

Aviv Amirav, Tel Aviv University and Aviv Analytical

Abstract

A Permethrin impurity was successfully analyzed by GC-MS with Cold EI after it failed to be analyzed by GC-MS with standard EI. In this application note we demonstrate and discuss the ways GC-MS with standard EI analysis of relatively large compounds gradually becomes more difficult as the sample compound size is increased due to reduced total ion count signal, reduced molecular ion relative abundance and increased noise. Accordingly, as the analyzed sample compound becomes larger its GC-MS analysis becomes harder in a gradual fashion until it fails. In contrast, GC-MS with Cold EI can analyze twice larger compounds and thus significantly extends the range of compounds amenable for GC-MS analysis.    

Open Probe Fast GC-MS - Real Time Analysis with Separation

Uri Keshet (1), Tal Alon (1,2) , Alexander B. Fialkov (1), and Aviv Amirav (1,2) 

1.   School of Chemistry, Tel Aviv University, Tel Aviv 69978, Israel.  

2.   Aviv Analytical Ltd, 3 Haarad Street, Tel Aviv 69107, Israel  

Abstract 

An Open Probe inlet was combined with a low thermal mass (LTM) ultra fast gas chromatograph (GC) and a mass spectrometer (MS) of a standard GC-MS for obtaining real time analysis with separation. The Open Probe is based on a vaporization oven that is open to room air with an addition of helium purge flow protection that eliminates air leakage into the oven, column and MS ion source. Sample introduction into the Open Probe is as simple as; touch the sample, insert the sample holder into the open probe oven and have the results in 30 s with under a minute ready for next analysis. 

The Open Probe Fast GC-MS revolutionizes the field of real time analysis as it provides several major benefits in comparison with DART, DESI and other ambient ionization methods or MS probes:

• GC separation,
• Library identification
• Absence of ion suppression effects
• Uniform electron ionization response for improved quantitation
• Uses a low cost quadrupole MS (of GC-MS). 

Watch the short video below and keep reading to find out more about the new Open Probe fast GC-MS which was combined with Agilent 7890B GC and 5977 MS and learn about its several demonstrated application and benefits. 

If the video doesn't show, you can click here to see it on Youtube.

What Can be Improved in GC-MS – When Multi Benefits are Transformed into a GC-MS Revolution

Aviv Amirav, Alexander B. Fialkov and Tal Alon, Tel Aviv University and Aviv Analytical

GC-MS vendors typically describe and characterize their systems using a small set of specifications that include octafluoronaphthalene (OFN) signal to noise ratio (SNR), mass range and scan speed. As a result, improvements in GC-MS are often focused on the incremental increase of these few specifications. However, GC-MS is characterized by many additional features and operational parameters that contribute to its performance, and their improvements can make a big impact on the GC-MS analytical capabilities. Many such GC-MS aspects are improved by incorporating the new Cold-EI GC and MS interface and ion source technology and by using "out of the box" thinking. In LC-MS, the biggest revolution was brought not by LC or MS improvements but rather by the development of a new interface and ionization method namely Electrospray. Similarly, Cold EI with its supersonic molecular beams interface and fly-through ion source brings multiple benefits and improvements into GC-MS which can initiate a new GC-MS revolution. This blog post lists 62 GC-MS improvements brought forth by the Cold EI interface and ion source, encompassing any and every important aspect of GC-MS, and explains how the unique features of GC-MS with Cold EI enable these benefits. 

Keep reading to find out how the 5975-SMB GC-MS with Cold EI improves GC-MS not by one or few but by 62 different aspects. When these multiple benefits are combined they are destined to be transformed into the next GC-MS revolution.  

Advanced GC-MS Presentations of Aviv Analytical in Pittcon 2013

Aviv Amirav and Tal Alon, Tel Aviv University and Aviv Analytical, Emails: amirav@tau.ac.il and polaris@tau.ac.il

In the 2013 Pittcon meeting (Philadelphia 17-21 March 2013) Prof. Aviv Amirav and Dr. Tal Alon will present six advanced GC-MS presentations performed mostly with the 5975-SMB GC-MS with Cold-EI. Brief abstracts of these presentations are given below (we will be happy to provide the full presentations upon request). 

We will be happy to meet you at our posters (240-11, 1210-6, 2180-3) or at the lecture halls after our oral presentations (1430-3, 2080-4, 2330-5) to discuss your advanced GC-MS needs and challenging applications, or any other topic.

Keep reading to find out how the Aviv Analytical 5975-SMB GC-MS with Cold EI brings the next GC-MS revolution and largely improves GC-MS performance for a broad range of applications. 

Tetryl Analysis using the 5975-SMB GC-MS with Cold EI

Aviv Amirav, Professor of Chemistry at Tel Aviv University and Director - Aviv Analytical Ltd

Introduction

Tetryl, (2,4,6-Trinitrophenylmethylnitramine, C7H5N5O8) is a sensitive explosive compound used to make detonators and explosive booster charges. Tetryl is produced by slowly mixing dimethylaniline with concentrated nitric acid in the presence of sulfuric acid and due to its simple synthesis it is prone for attempted synthesis by terrorists. Tetryl is a thermally labile explosives that is known to be difficult to analyze by GC-MS due to its degradation at the GC injector and at the GC column to N-methylpicramide through a loss of NO and a gain of hydrogen from the column PDMS film. As a result, the analysis of Tetryl is challenging. 

   

We received a sample of Tetryl that was synthesized by A.I. Explosives, Inspection & Services Company (www.aiexplosives.com) that attempted to follow terrorist's synthetic roots and characterize it via the tetryl synthetic impurities.   

In this post we present the uniquely successful analysis of Tetryl perform with Aviv Analytical's 5975-SMB GC-MS.    

Very Fast Heroin Analysis – The Role of Flow Programming

Aviv Amirav, Professor of Chemistry at Tel Aviv University and Director – Aviv Analytical 

Introduction 

Forensic laboratories are often confronted with a need to analyze hundreds of "white powders" for the presence of drugs of abuse or otherwise to determine their harmless nature. However, a typical "fast" analysis utilizing a standard GC-MS can take 20 minutes (full analysis cycle time including chromatography and cooling back for the initiation of next analysis). Thus, there is a growing need for improved instruments and methods that are capable of much faster analysis cycle times, while retaining good separation and high quality mass spectra for identification purposes.    

Heroin, like many other drugs of abuse, is sold in the streets as a powder mixture which typically contains paracetamol (also named acetaminophen) and caffeine as its major ingredients and a few percents each of 6-monoacetylmorphine (coeluting with some acetylcodeine), heroin, papaverine and noscapine in order of their GC elution times. Thus, a fast street heroin analysis must preserve the proper separation of all its major ingredients while providing full separation of the heroin itself for its quantitation and eluting the last to elute noscapine and anything else that might otherwise contaminate the column. 

In this post we present the details of our rapid analysis of heroin.