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.
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.
Recent Posts
EPH Fractionation & Bottlenecks in the Laboratory
November 4, 2022 at 6:49 PM / by Matt Harden
Anyone familiar with Extractable Petroleum Hydrocarbons (EPH) methods such as those developed by Massachusetts DEP, New Jersey DEP, or one of the other various state agencies that regulate EPHs is familiar with the long and grueling process of fractionation.
The Problem of PFAS: Part 4 - Tracking Contamination
February 3, 2022 at 4:00 PM / by Matt Harden
Welcome to part 4 of our blog series “The Problem of PFAS”. If you are just tuning in, you might want to take a look at the previous blogs of this series as we provided background on the PFAS controversy (Part 1), a review of the regulatory guidelines for monitoring PFAS contamination in the environment (Part 2), and most recently, a look at which analytical method might work the best for your lab (Part 3). If you are up to speed on this series, you should now have a good baseline on what we’ll be discussing today.
Testing for toxic organic contaminants in environmental samples often requires the following three sample preparation steps: 1) Extraction, 2) Concentration, and 3) Analysis. The goal during these three steps is to isolate the contaminants from the sample matrix and concentrate them so they can be detected and quantified. In this blog, I will discuss the importance of understanding how different types of concentration equipment can impact your analyte recoveries and the overall performance of your extraction procedure.
The Problem of PFAS: Part 3 - Which PFAS Method is Right for Me?
September 22, 2021 at 3:55 PM / by Matt Harden
Welcome to part 3 of our blog series “The Problem of PFAS”. If you are just tuning in, you might want to take a look at the previous blogs of this series as we provided background on the PFAS controversy (Part 1) as well as a review of the regulatory guidelines for monitoring PFAS contamination in the environment (Part 2). If you are up to speed on this series, you are now ready to dive deeper into the specific methods for monitoring PFAS in the environment.
How to plan for dirty samples for both extraction and analysis
December 16, 2020 at 9:39 AM / by Matt Harden
When juggling the responsibilities of working in a sample preparation lab as well as working as an analyst, it is very easy to get caught up in a never-ending cycle of samples. There is no situation “more frustrating” then when you have a bunch of wastewater samples that need to be extracted and analyzed ASAP and there is that one sample that is so much more challenging to extract than the others.
Overcoming drying and concentrating bottlenecks in the lab
December 15, 2020 at 11:33 AM / by Matt Harden
Working in an environmental lab requires a lot of concentration, both mentally and for the samples that you are working with. When New England finally begins to thaw and local companies rush to get their samples completed, a bottleneck that is usually experienced is the drying and concentration of so many samples.
When working in a contract lab or any analytical testing lab, you may be prone to periods where it seems like there is never going to be a light at the end of the tunnel, as the samples just keep on coming in.
What are the differences between EPA Method 533 vs 537.1?
December 7, 2020 at 2:02 PM / by Matt Harden