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Matt Harden

EPH Fractionation & Bottlenecks in the Laboratory

December 7, 2020 at 1:38 PM / by Matt Harden

Anyone familiar with EPH methods such as those developed by the Massachusetts or New Jersey Department of Environmental Protection is familiar with the long and grueling process of fractionation.

For those unfamiliar, with EPH or Extractable Petroleum Hydrocarbons it is an extraction that essentially occurs in two distinct parts: the initial extraction & concentration and then the fractionation of that initial extract into the aromatic and aliphatic fractions followed by concentration again. EPH is a method that replaces the TPH (Total Petroleum Hydrocarbons) or 8015 methods and allows for the calculation of specified carbon ranges giving you a more accurate assessment of potential health risks.

The fractionation process can be a particularly frustrating procedure for laboratories that run this methodology. Many labs will not utilize vacuum processing to facilitate this fractionation and will rely on gravity flow of the solvents through the silica gel cartridge. This process does take quite a bit of time and it is driven by manual techniques. For example, if I were to perform a full aqueous extraction for EPH using 8 separatory funnels, it would take me the better part of a day and a quarter to get those 3 quality control and 5 customer samples extracted. The fractionation portion itself would take up more than half of that time and in the end, I would only complete 5 customer samples to be analyzed on the GC FID that day.

Don’t even get me started on having to make sure your solvent measurements are accurate from lot to lot by performing a fractionation check for each new lot of cartridges only to have it fail and prevent any further progress on my work. Another bottleneck in completing extractions was when the fractionation did not work perfectly, and breakthrough of one set of compounds into the wrong fraction occurred and you had to perform a re-fractionation. It was extremely challenging having to run back to the extractions lab and perform the whole fractionation process over again especially when you had deadlines.

So, as you can see fractionation is already a bit of a bottleneck even without the numerous issues with variation of media between different lots of cartridges. To add to that headache, the results from technician to technician may vary meaning that if your normal lab tech is out sick and someone less practiced in the art has to fill in, you may see different results from what you’d expect. As someone who has used a variety of different fractionation cartridges throughout the years, the main thing I want is consistency, so you don’t have to waste any more time on an already laborious process. Out of all the brands I’ve encountered while working in the laboratory, the Biotage ISOLUTE® EPH cartridge has been the Advil to help alleviate my headache.

SPE-EPH Fractionation & Bottlenecks-ISOLUTE-CartridgesWith the ISOLUTE® EPH brand cartridge, I hardly saw a difference in data from when a 3-year veteran fractionated compared to the technician that I just started training 3 weeks earlier. As an added benefit the fractionation checks were a breeze and inspired confidence that each lot of cartridges were consistent and would not cause us to drop whatever we were doing to re-fractionate a failed sample. Even during the best stretches of fractionation with other brands, I still experienced occasional breakthrough and fractionation check issues requiring us to frequently adjust the method. The proprietary blend of silica and alumina in the ISOLUTE® EPH cartridge helped eliminate one of my worst enemies of sample breakthrough and helped to keep the extractions lab moving forward instead of stuck in neutral.

Download our latest technical note including a chemistry data sheet on the ISOLUTE® EPH solid-phase extraction cartridge.

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To watch my webcast on EPH fractionation when using ISOLUTE® EPH cartridges, click the video link below.

 

Topics: EPA Method, Fractionation

Matt Harden

Written by Matt Harden

Matt is an Applications Chemist at Biotage. In his current role, Matt supports the pre-sales and post-sales team, the marketing team, and clients in order to provide customer service for a wide range of solid-phase extraction and evaporation/concentration systems. Matt also helps to research ways of optimizing the extraction processes used for solid-phase extraction and then develop application notes based on that research. Matt received his Bachelor of Science in Biology with a minor in Chemistry from Western New England University and possesses a Master of Healthcare Administration from Mass College of Pharmacy and Health Sciences. In his prior role working in an environmental contract laboratory, he was able to experience the first-hand experience in the manual extraction, concentration, and analysis of a variety of EPA regulated methods such as 608.3, 625.1, 8015, 8081/8082, and 8270D among other methods. Matt also has prior experience in application sciences for a variety of other environmental instrumentation.

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