EU Regulation 396/2005: Pesticide Residue Testing and the Critical Role of QuEChERS Evaporation in Food Safety

<p><strong>Our Library never stops expanding. What are the most recent contributions to LabRulezGCMS Library in the week of 4th May 2026? Check out new documents from the field of the gas phase, especially GC and GC/MS techniques!</strong></p><blockquote><p><span style="font-size:20px;">👉 </span><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library"><span style="font-size:20px;"><strong>SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT GCMS AND RELATED TECHNIQUES</strong></span></a></p></blockquote><blockquote><p><strong>👉 Need info about different analytical techniques?</strong> Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library"><strong>LabRulezLCMS</strong></a> or <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library"><strong>LabRulezICPMS</strong></a> libraries.</p></blockquote><p>This week we bring you application note by<strong> Shimadzu, </strong>presentation by <strong>MDCW / JEOL</strong> and technical note by <strong>Thermo Fisher Scientific!</strong></p><h3><strong>1. MDCW / JEOL: Flow-Modulated GCxGC-QMS Analysis Without Splitting Off the GC Flow</strong></h3><ul><li>Presentation</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/labrulez-bucket-strapi-h3hsga3/O_16_Jensen_11e29d5022.pdf"><strong>Full PDF for download</strong></a></li></ul><section><div><div><div><div><div><div><p>This presentation by Kirk Jensen (JEOL USA) explores the feasibility of performing <strong>flow-modulated comprehensive two-dimensional gas chromatography (GC×GC) coupled with quadrupole mass spectrometry (QMS)</strong> without splitting the GC flow, which is traditionally required to protect MS systems from high carrier gas flows. The core concept builds on GC×GC, where compounds are separated using a primary and secondary column connected via a modulator, significantly increasing separation power compared to one-dimensional GC. The presentation contrasts <strong>thermal modulation</strong> (offering sharper peaks and higher theoretical sensitivity but requiring cryogenic cooling) with <strong>flow modulation</strong>, which avoids cryogens, handles volatile analytes well, and is more flexible, but typically demands higher gas flows that standard MS systems cannot tolerate .</p><p>To address this limitation, the study utilizes the <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?manufacturerItems=24&amp;search=JMS-Q1600GC"><strong>JEOL JMS-Q1600GC</strong></a><strong> UltraQuad quadrupole GC-MS system</strong>, which can accept unusually high carrier gas flows (up to ~20 mL/min), enabling direct coupling with a <strong>SepSolve INSIGHT flow modulator</strong> without splitting the effluent . The analytical setup includes dual GC columns (e.g., Zebron ZB-5MSplus for the first dimension and BPX50 for the second), high secondary flow rates (~25 mL/min), and electron ionization (EI) MS detection. Additional system components include optional FID detection, bleed line control, and ChromeSpace software for data processing . This configuration allows full analyte transfer into the MS, eliminating the need for flow splitting and potentially improving detection efficiency.</p><p>Experimental results demonstrate the applicability of this approach to complex mixtures, including a <strong>pesticide mixture containing over 200 compounds</strong> and real-world samples such as perfumes and fuels. The GC×GC-MS system produced detailed two-dimensional chromatograms with high spectral quality, enabling the correct identification of approximately 120 compounds despite relatively moderate spectral match factors . Comparisons at different flow rates (e.g., 25 vs. 50 mL/min) showed that spectral integrity and compound identification remain robust, indicating that higher flow operation does not significantly compromise MS performance.</p><p>In conclusion, the work demonstrates that <strong>flow-modulated GC×GC-QMS without flow splitting is feasible</strong>, provided that the MS system can tolerate high carrier gas flows. While further optimization is needed (e.g., column selection, inlet pressure, and separation conditions), the approach offers a practical alternative to thermal modulation by eliminating cryogens and simplifying operation. Future work will focus on improving sensitivity, optimizing separations, and exploring alternative carrier gases such as hydrogen to reduce costs and expand applicability</p></div></div></div></div></div></div></section><h3><strong>2. Shimadzu: Detailed Hydrocarbon Analysis by Nexis GC-2030 Using ASTM D6730</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_00863_en_eb633bc741.pdf"><strong>Full PDF for download</strong></a></li></ul><h5><strong>User Benefits</strong></h5><ul><li>Detailed compositional analysis of gasoline in accordance with ASTM D6730 is feasible using the Nexis GC-2030.&nbsp;</li><li>By employing PONAsolution, a PONA/DHA analysis software, laborious identification tasks can be reduced, and quantitation calculations and report generation can be performed automatically.</li></ul><p>ASTM D6730 specifies the analysis of hydrocarbons in gasoline and oxygenates such as ethanol, methyl tert-butyl ether (MTBE), and ethyl tert-butyl ether (ETBE) over a boiling point range up to 225 ̊C. Identification and quantification of individual compounds in gasoline are critically important for refinery process control and product quality assurance. In this application news, we report compositional analysis of gasoline conforming to ASTM D6730 using the <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=1&amp;search=Nexis+GC-2030"><strong>Nexis GC-2030 gas chromatograph</strong></a>. Gasoline typically comprises over 100 hydrocarbons, making identification tasks highly complex; however, PONAsolution, a PONA/DHA analysissoftware,simplifies this process.</p><h4><strong>PONAsolution</strong></h4><p>PONAsolution Ver.6 provides retention index libraries for each relevant standard (ASTM D6730, D6729, D5134, D6733). Identification of n-alkanes automatically corrects the retention times of the remaining several hundred components, thus streamlining the identification process. When only a specific retention region requires adjustment, the two-point identification function is useful (Fig. 1). In the two-point identification procedure, reference and sample chromatograms are compared while assigning corresponding peaks. First, click on an identified component mark in the reference data (Fig. 1, a), then click the matching sample peak (Fig. 1, b). Repeat this for a second pair of peaks. The retention times of components between these two anchor points are then automatically corrected.</p><h4><strong>Conclusion</strong></h4><p>Compositional analysis of gasoline in accordance with ASTM D6730 was performed. The combination of SH PONA Tuning Column and SH-1 PONA main column enabled separation of compounds with closely spaced retention times. Moreover, use of PONAsolution software greatly simplifies complex identification tasks.</p><h3><strong>3. Thermo Fisher Scientific: Fiber optic probes add flexibility to Raman chemical analysis</strong></h3><ul><li>Technical note</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/labrulez-bucket-strapi-h3hsga3/drx3_flex_tech_note_tn54708_bebb56b870.pdf"><strong>Full PDF for download</strong></a></li></ul><p>Fourier Transform Infrared Spectroscopy (FTIR) and Raman Spectroscopy are non-destructive analytical techniques that rely on the interaction of electromagnetic radiation with molecular vibrations to provide information about the chemical composition and structure of a sample. Despite their similarities, there are some distinct differences between the two techniques. In principle, FTIR is based on the absorption of infrared radiation by molecules and measures changes in dipole moment during molecular vibrations. Raman spectroscopy, on the other hand, is based on the inelastic scattering of monochromatic light and measures changes in polarizability during molecular vibrations.&nbsp;</p><p>When applied to bulk chemical analysis, both FTIR and Raman spectroscopy can be used to analyze solids, liquids, and gases, but the nature of Raman spectroscopy lends some unique sampling advantages. Additionally, Raman often requires little to no sample preparation. Presented herein are application examples that highlight some of the sampling advantages of Raman spectroscopy. All the spectral data in this technical note were collected using a <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/products/2238"><strong>Thermo Scientific™ DXR3 Flex Raman Spectrometer</strong></a> equipped with a fiber optic probe. (Fiber optics are readily available for Raman spectroscopy because of the use of visible and NIR light and do not require the exotic materials associated with FTIR fiber optics.) Preliminary tests for all samples were carried out using both 532 nm and 785 nm excitations, and it was determined that the 785 nm laser set gave an overall better balance between fluorescence and Raman scattering efficiency.</p><h4><strong>Summary&nbsp;</strong></h4><p>In this technical note, the analyses of a variety of samples by Raman spectroscopy are demonstrated. All samples were analyzed without sample preparation.&nbsp;</p><ul><li>Precise and localized analysis at the focal point of the Raman-exciting laser allows sampling through glass bottles, blister packaging and plastic containers, which eliminates possible cross contamination and analyst exposure to hazardous materials. The contributions from the packaging and containers depend on the type of container material, the container thickness, and the materials’ chemical compositional complexity, but these contributions can be readily subtracted out when needed.&nbsp;</li><li>Water is a weak Raman scatterer. Raman therefore has reduced water sensitivity, making it a preferred technique for aqueous solution analysis over FTIR. As demonstrated in the analysis of an energy drink, the Raman bands from water can be subtracted from the spectrum of the aqueous solution, leading to the identification of the components of the solution.&nbsp;</li><li>Raman spectroscopy is well suited for the analysis of inorganic materials, especially in identifying the crystal phases and polymorphs, as demonstrated by the analyses of minerals and pigments in a painting.&nbsp;</li><li>Fiber optic probes provide flexibility and ease of maneuverability. This is particularly advantageous when analyzing samples that are difficult to access or manipulate, such as large containers, geological samples and paintings</li></ul><p>The DXR3 Flex has multiple sampling options available. A properly configured fiber-optic probe is arguably the most versatile accessory for the analysis of bulk solids and liquids. The advantages, both from those inherent to Raman spectroscopy and those resulting from the use of fiber optic probe, provide opportunities for a wide variety of different applications when using the DXR3 Flex Raman Spectrometer.</p>

News from LabRulezGCMS Library - Week 19, 2026

<p><strong>🎤Francis Femi Oloy</strong></p><p><strong>In this episode of Concentrating on Chromatography, David speaks with Francis Femi Oloy about using chromatography to uncover hidden pollutants in real-world water systems.</strong></p><p>Femi’s team analyzed polychlorinated biphenyls (PCBs) in six major rivers in southwestern Nigeria — compounds that were banned decades ago but still persist in the environment. Using a workflow that many analytical labs will recognize — liquid–liquid extraction, cleanup, rotary evaporation, nitrogen blowdown, and GC-ECD detection — they quantified 25 PCB congeners at trace levels and linked the results to ecological and human health risk.</p><h4><strong>In this conversation, we cover:</strong></h4><ul><li>Why legacy pollutants like PCBs still show up today</li><li>Choosing GC-ECD vs LC-MS for halogenated compounds</li><li>Liquid–liquid extraction and matrix cleanup strategies</li><li>Why sample concentration is critical for dilute environmental samples</li><li>How rotovap + nitrogen blowdown work together without losing volatile analytes</li><li>Seasonal trends (why wet season levels were higher)</li><li>Translating concentration data into meaningful risk assessments</li></ul><h3><strong>Video Transcription</strong></h3><section><div><div><div><div><div><div><p><strong>Persistent organic pollutants</strong> such as polychlorinated biphenyls (<strong>PCBs</strong>) remain a significant environmental concern despite decades of regulatory restrictions. In this interview, Francais Femi Oloy discusses the environmental and analytical challenges associated with monitoring PCB contamination in rivers of southwestern Nigeria, a rapidly industrializing region where urban growth, industrial activity, agriculture, and dense populations intersect with extensive aquatic systems.</p><p>Oloy explains that his interest in environmental contaminant analysis emerged from observing unexplained health problems and environmental degradation while growing up in Nigeria. This motivated his transition into organic and environmental chemistry, with a focus on identifying pollutants present in drinking water, agricultural soils, and food systems. Southwestern Nigeria, particularly the Lagos region, represents a critical environmental monitoring area due to intense industrial development, shipping activity, and widespread human dependence on rivers for domestic use, agriculture, and fishing.</p><p>Although PCBs are considered “<strong>legacy pollutants</strong>” and are no longer intentionally produced, the interview highlights why they continue to persist in aquatic environments. Old electrical transformers and aging industrial equipment still contain PCB residues, while historical contamination stored in river sediments can become remobilized during flooding, dredging, or sediment disturbance. Because PCBs are hydrophobic and resistant to degradation, they preferentially accumulate in sediments and bioaccumulate through aquatic food chains, creating long-term environmental and human exposure risks.</p><p>A major focus of the discussion centers on the analytical workflow used for PCB determination in environmental water samples. Composite river water samples were collected in amber glass bottles to avoid contamination and photodegradation, preserved with sodium azide to minimize microbial activity, and stored under cooled conditions prior to extraction. The analytical protocol employed <strong>liquid–liquid extraction</strong> using dichloromethane (DCM) and hexane to recover both polar and nonpolar PCB congeners. Oloy emphasizes that liquid–liquid extraction was selected over solid-phase extraction (SPE) because of concerns about congener retention within sorbent materials and clogging issues associated with large-volume environmental samples.</p><p>Following extraction, concentration and cleanup represented critical analytical stages due to the trace-level occurrence and volatility of PCBs. Silica and alumina cleanup procedures were used to remove matrix interferences prior to instrumental analysis. The concentration workflow combined rotary evaporation for bulk solvent reduction with nitrogen blowdown for final volume reduction to less than 1 mL, while carefully avoiding excessive temperature or complete dryness to minimize analyte loss. Oloy repeatedly stresses that improper concentration procedures are among the most common causes of analytical failure in PCB analysis.</p><p>For instrumental determination, the study utilized <strong>gas chromatography coupled with electron capture detection (GC-ECD)</strong> rather than LC-MS or GC-MS. According to Oloy, GC was preferred because PCBs are sufficiently volatile for gas chromatographic separation, while ECD provided superior sensitivity and selectivity for chlorinated compounds at environmentally relevant concentrations. The interview also discusses analytical validation strategies, including the use of surrogate standards to assess <strong>recoveries,</strong> which ranged from approximately <strong>85% to 114%</strong>, and signal-to-noise-based determination of detection limits.</p><p>The study further examined <strong>seasonal variations in PCB concentrations</strong>, revealing <strong>higher levels during the wet season</strong>. This observation was attributed to rainfall-driven runoff from contaminated infrastructure, sediment resuspension, and lower temperatures that reduce volatilization losses. To communicate toxicological relevance beyond simple concentration reporting, the researchers also calculated <strong>toxic equivalency values (TEQs)</strong>, converting mixtures of PCB congeners into biologically meaningful toxicity estimates comparable to dioxin toxicity metrics.</p><p>Beyond environmental monitoring, Oloy highlights broader research interests focused on <strong>pollutant remediation and sustainable environmental protection</strong>. His group is also involved in developing catalytic materials capable of degrading or removing persistent contaminants from environmental systems. Throughout the discussion, he emphasizes that analytical chemistry plays a central role not only in detecting pollutants, but also in enabling prevention, remediation, and long-term environmental management strategies.</p></div></div></div></div></div></div></section><blockquote><p><strong>This text has been automatically transcribed from a video presentation using AI technology. It may contain inaccuracies and is not guaranteed to be 100% correct.</strong></p></blockquote><blockquote><h4><strong>Concentrating on Chromatography Podcast</strong></h4><p>Dive into the frontiers of chromatography, mass spectrometry, and sample preparation with host David Oliva. Each episode features candid conversations with leading researchers, industry innovators, and passionate scientists who are shaping the future of analytical chemistry. From decoding PFAS detection challenges to exploring the latest in AI-assisted liquid chromatography, this show uncovers practical workflows, sustainability breakthroughs, and the real-world impact of separation science. Whether you’re a chromatographer, lab professional, or researcher you'll discover inspiring content!</p><p>You can find <strong>Concentrating on Chromatography Podcast </strong>in podcast apps:</p><ul><li><a target="_blank" rel="noopener noreferrer" href="https://open.spotify.com/show/1wZg67rCjoGju4yhqxI3tL"><strong>Spotify</strong></a></li><li><a target="_blank" rel="noopener noreferrer" href="https://podcasts.apple.com/tz/podcast/concentrating-on-chromatography/id1788429185"><strong>Apple podcast</strong></a></li><li><a target="_blank" rel="noopener noreferrer" href="https://podscan.fm/podcasts/concentrating-on-chromatography"><strong>podscan</strong></a></li></ul><p>and on <a target="_blank" rel="noopener noreferrer" href="https://www.youtube.com/@ChromatographyTalk/videos"><strong>YouTube channel</strong></a></p></blockquote>

Tracking Toxic PCBs in River Water using Gas Chromatography–Electron Capture Detection

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<p><strong>There is a general perception that gas chromatography (GC) and the various forms of detection that are used with this technique have developed to the point where it is now a “mature” technology, but GC practitioners know that there are many new challenges to face and that new solutions are required to overcome longstanding issues.</strong></p>
<p>This virtual symposium, organized by the Chromatographic Society (ChromSoc) and LCGC, will focus on areas of GC where the sample complexity, the requirements for highly accurate measurements, the sensitivity requirements imposed by regulators, and the need to push scientific discovery force GC users to look with fresh eyes on this supposedly “mature” technique. The highly respected international speakers will bring a fresh perspective on almost every aspect of GC in the vapour phase and the virtual symposium will maintain the high reputation that this bi-annual meeting has established over many years.</p>
<h3><strong>Key Learning Objectives:</strong></h3>
<ul>
<li>Modern approaches to achieving ultratrace detection limits in GC and GC–MS are revealed</li>
<li>The use of GC and GCxGC with high-resolution MS for complex sample screening will be discussed</li>
<li>Learn about advanced techniques for sample preparation and enrichment for qualitative and quantitative analysis</li>
</ul>
<h3><strong>Who Should Attend:</strong></h3>
<p>Anyone working with GC who wants to understand the very latest approaches to achieving ultratrace analyte quantitation, sample preparation, and enrichment for complex matrices and reducing error in quantitative GC analysis.</p>
<h3><strong>Agenda:</strong></h3>
<ul>
<li><p><strong>12pm BST = 7am EDT Symposium Introduction</strong> (Tony Taylor, Arch Sciences Group, UK)</p>
</li>
<li><p><strong>12:30pm BST = 7:30am EDT High Resolution GC–MS and GC×GC–MS with Advanced Data Processing for Investigative Compositional Analysis</strong> (Hans-Gerd Janssen, Unilever and Wageningen University, The Netherlands)</p>
</li>
</ul>
<h4><strong>Technology Session 1</strong></h4>
<ul>
<li><p><strong>1:10pm BST = 8:10am EDT Hydrogen Carrier Gas for Fast GC: Choosing the right setup for your GC</strong> (Ed Connor, Product Manager, PEAK Scientific)</p>
</li>
<li><p><strong>1:25pm BST = 8:25am EDT Derivatization and Traceable Quantification—A Match Made in Hell?</strong> (Chris Hopley, LGC’s National Measurement Laboratory, UK)</p>
</li>
</ul>
<h4><strong>Technology Session 2</strong></h4>
<ul>
<li><p><strong>2:05pm BST = 9:05am EDT Low-Pressure Gas Chromatography (LPGC)–The Fast Way to Your Pesticide Analysis</strong> (Dr. Jana Hepner, Applications Scientist, Restek)</p>
</li>
<li><p><strong>2.20pm BST = 9:20am EDT Meeting the Analytical Challenges of Environmental Monitoring for the Water Framework Directive: Quantifying a Drop (or Two) in the Ocean</strong> (John Quick, ALS Environmental, UK)</p>
</li>
</ul>
<h4><strong>Technology Session 3</strong></h4>
<ul>
<li><p><strong>3pm BST = 10am EDT VICI Fast Temperature Programmer Methods and Applications</strong> (Dale Ashworth, Product Manager Analytical Systems, VICI)</p>
</li>
<li><p><strong>3:15pm BST = 10:15am EDT Is the E&amp;L Community Ready to Move Away from Conventional Large Volume Liquid–Liquid Extraction and Solvent Evaporation?</strong> (Mike Hodgson, Baxter, UK)</p>
</li>
</ul>
<h4><strong>Technology Session 4</strong></h4>
<ul>
<li><p><strong>3:55pm BST = 10:55am EDT Raise the Bar of Trace Analysis: Simultaneous high quality target and non-target data are within reach</strong> (Liz Humston-Fulmer, Application Chemist, LECO Corporation)</p>
</li>
<li><p><strong>4:10pm EDT = 11:10am EDT Combining Automated Green and Exhaustive Enrichment Techniques with 1D GC–TOF–MS for Untargeted Aroma Profiling of Food/Beverages and Consumer Products in QA/QC Industrial Laboratories</strong> (Tatiana Cucu, Research Institute of Chromatography)</p>
</li>
<li><p><strong>4:50pm BST = 11:50am EDT Technology Session 5</strong></p>
</li>
<li><p><strong>5:05pm BST = 12:05pm EDT Technology Session 6</strong></p>
</li>
<li><p><strong>5:20pm BST = 12:20pm EDT Panel Discussion</strong></p>
</li>
</ul>


ChromSoc: Advances in Gas Chromatography: A Virtual Symposium

Advances in Gas Chromatography: A Virtual Symposium

<p><strong><a href="https://gcms.cz/products?search=pegasus&amp;manufacturerItems=24&amp;instrumentationItems=3">LECO&#39;s Pegasus®</a> line is designed to take full advantage of the speed of TOFMS analyses without sacrificing the sensitivity you need, and our<a href="https://gcms.cz/library?search=+stayclean&amp;mainauthorItems=24"> StayClean®</a> Ion Source means you never have to slow down to clean out your engine.</strong></p>
<p>The advantages of helium as a carrier gas for mass spectrometers have long been known, but it is a limited natural resource with varied supplies and expenses. On the other hand, hydrogen gas generators can be installed in any lab for a constant supply and, conveniently, increased chromatographic speeds.</p>
<p>Join LECO&#39;s panel of experts for a one-day forum to discuss how to overcome the challenges of switching from helium to hydrogen, the analytical and business impacts of adding hydrogen generators to your lab, and how the resulting mass spectral profiles compare between helium and hydrogen gases.</p>
<h3><strong>Forum Talks</strong></h3>
<h4><strong>Fast GC/Hydrogen Method Transfer Overview &amp; Application Examples</strong></h4>
<p>Helium is a limited natural resource with huge variations in both supply and expense. At the same time, the advantages of hydrogen to achieve increased chromatographic throughput in GC applications is attractive. The transferral of methods to hydrogen carrier gas can be problematic due to limitations and challenges associated with some types of mass spectrometry technology used. In particular, the mass spectral quality and fragmentation, in comparison with that obtained using helium, as well system sensitivity and also, system robustness and acquisition rate are important factors which can differ and negatively affect results. In this study we have investigated the use of a particular type of GC-TOF-MS technology in regards to overcoming these issues. The method transfer approach, technology benefits, and application examples are presented.</p>
<blockquote>
<p><strong>Presenter: Nick Jones an David Benanou</strong></p>
</blockquote>
<h4><strong>Flow Modulated Fast Comprehensive Two-Dimensional Gas Chromatography Combined With Time-of-Flight Mass Spectrometry: A Comparison Between the use of Helium and Hydrogen as Carrier Gas</strong></h4>
<p>The present research is focused on the comparison between the use of hydrogen and helium carrier gases, within the context of flow-modulation fast comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry. All experiments were carried out by using the following column set: low polarity with dimensions 10 m × 0.25 mm ID × 0.25 µm df and medium polarity with dimensions 2 m × 0.10 mm ID × 0.10 µm df. Fundamental gas chromatography parameters (efficiency, resolution) were measured under different experimental conditions, using the two carrier gases. Efficiency was measured in both the first (using C12 alkane) and second (using naphthalene) dimensions; after defining the optimum carrier gas conditions, a sample of diesel was analyzed, with the overall separation evaluated to make final conclusions on the analytical performances. Finally, a comparison was made between mass spectral profiles obtained analyzing fatty acid methyl esters and pesticides.</p>
<blockquote>
<p><strong>Presenter: Peter Q. Tranchida and Luigi Mondello (University of Messina, Messina, Italy)</strong></p>
</blockquote>
<h4><strong>Switch to Fast GC Easily - Theory and Practice</strong></h4>
<p>There a number of ways that the analysis time can be reduced. It all depends on how well the components are separated in the present application. Most easy is to trade in some resolution for speed using higher gas velocities or using a shorter column. If the exact separation must be maintained, a choice has to be made between using hydrogen as carrier gas, or use a smaller ID capillary column (or a combination). What is important is that in the new method, the same chromatogram (and peak elution order) must be obtained. Using the EZGC method translator, you can simply calculate the oven program you need for that. Also, in the ProEZGC chromatogram modeler, you can see the impact of any changed parameter, just using your laptop.</p>
<blockquote>
<p><strong>Presenter: Jaap de Zeeuw (Restek)</strong></p>
</blockquote>
<h4><strong>Advantages of Hydrogen Generators: Usage, Costs, and Safety Made Easy</strong></h4>
<p>Analytical laboratories use a variety of analytical techniques as part of their research and development and quality control of products. Many of these processes require high purity gases, many of which can be produced by gas generators. For a number of reasons, including safety, cost, convenience, and analytical throughput, more and more labs are abandoning hydrogen cylinders in favor of hydrogen gas generators to supply the gases they require for their analyses. During this session, Jean-Marie Casanova will cover analytical and business impacts about implementing Hydrogen gas generators in your lab.</p>
<blockquote>
<p><strong>Presenter: Jean-Marie Casanova (Sales Director, F-DGSi)</strong></p>
</blockquote>


GCMS webinars focusing on Gas Generators, GCxGC - page 1

Designed for Speed: A Fast-GC Forum

Advances in Gas Chromatography: A Virtual Symposium

Related content

Tracking Toxic PCBs in River Water using Gas Chromatography–Electron Capture Detection

EU Regulation 396/2005: Pesticide Residue Testing and the Critical Role of QuEChERS Evaporation in Food Safety

News from LabRulezGCMS Library - Week 19, 2026