Visit the LabRulez booth at <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/events/871">analytica 2026</a> in Munich, 24. - 27. March 2026! You can find us in Hall A1, Booth A1.506. At the booth, you will be able to explore live demonstrations of how the LabRulez portals work and see selected analytical instruments from our pre-owned marketplace section.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Lab_Rulez_at_Analytica_2026_Floor_plan_55e1057e03.jpg" alt="LabRulez at Analytica 2026: Hall A1 Floor Plan and Booth Location" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Lab_Rulez_at_Analytica_2026_Floor_plan_55e1057e03.jpg 245w," sizes="100vw" width="1516" height="881"><h3>Would you like to learn how the LabRulez portals work?</h3>➡︎ <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/">LabRulezLCMS</a> ➡︎ <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/">LabRulezGCMS</a> ➡︎ <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/">LabRulezICPMS</a><ul><li>A unique online solution for your marketing</li><li>A targeted audience from the analytical chemistry community</li><li>Modern technologies and a unique concept</li><li>Design optimized for most smart devices – PC, mobile, and tablet</li><li>Advanced statistical tools fully available to users</li></ul><h3>Services Offered</h3><h4>News + Company Updates</h4><ul><li>Publish news related to your instrumentation, applications, services, events, job openings, and more</li><li>News is shared both on our portals and across our social media channels</li></ul><h4>Library – All Documents in One Place</h4><ul><li>Applications, posters, presentations, technical articles, brochures, specifications</li><li>Fast and advanced search capabilities</li><li>Over 32,000 documents currently available in our database</li></ul><h4>Webinars</h4><ul><li>Upcoming and on-demand webinars from the field of analytical chemistry</li><li>More than 5,500 webinars covering chromatography, mass spectrometry, and spectroscopy</li></ul><h4>Careers</h4><ul><li>Targeted job listings in analytical chemistry</li><li>Clear filtering by specialization or location</li><li>Increased visibility for job postings</li></ul><h4>Companies</h4><ul><li>Company profile with key information and contacts</li><li>Integration of all your activities on our portal: News, Library documents, Webinars, Upcoming Events, Careers, and mentions by partners or customers</li><li>Connection to your Products listed on LabRulez portals</li></ul><h4>Products and Services</h4><ul><li>Comprehensive overview of instrumental techniques and services</li><li>Targeting the analytical chemistry community and customers in the growing online environment</li></ul><h4>Marketplace</h4><ul><li>Buying and selling pre-owned analytical equipment</li><li>We purchase analytical instrumentation of all brands and ages</li><li>Sell your equipment through LabRulez</li><li>Request and purchase complete systems, modules, or spare parts with warranty and service</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Lab_Rulez_at_analytica_2026_bazar_7edf4a0872.jpg" alt="LabRulez at analytica 2026" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Lab_Rulez_at_analytica_2026_bazar_7edf4a0872.jpg 88w," sizes="100vw" width="1600" height="2844"><h3>What Will Be on Display at Our Booth?</h3>Come and explore selected spare parts and modules from our marketplace section. These include both new, tested, and pre-owned items.<h4><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar">LabRulezLCMS Marketplace</a></h4>Spare parts for LC/MS:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar?category=378">Vacuum turbo pumps for LC/MS</a></li></ul>Spare parts for HPLC:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar?category=397">Degassers for HPLC/UHPLC</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar?category=368&amp;search=valve">Automatic valves for HPLC</a></li><li>HPLC components for Agilent 1100, 1200, and 1260 Infinity II series</li></ul>Consumables:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar?category=377">HPLC lamps</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/bazaar?category=48">HPLC columns</a></li></ul><h4><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/bazaar">LabRulezGCMS Marketplace</a></h4>Spare parts for GC/MS:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/bazaar?category=367&amp;search=turbo">Turbo pumps for GC/MS</a></li></ul>Spare parts for GC:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/bazaar?category=366&amp;search=EPC">EPC modules</a></li></ul>Sample injection<ul><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/bazaar/432">Autosampler 7693A for GC</a></li></ul>Consumables:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/bazaar?category=7">GC columns </a>and selected accessories</li></ul>

LabRulez at analytica 2026

🎤Alex BrodyIn this episode of Concentrating on Chromatography, we sit down with Alex Brody, an organic chemist at Aqua America, to discuss the rigorous analytical methods required for regulated drinking water testing.Alex walks us through the multi-step PFAS detection process using EPA Method 537.1, including extraction, nitrogen blowdown concentration, and LC-MS analysis. He explains why sample preparation and quality control are critical for achieving trace-level detection—and why these methods can't be rushed or simplified, even with new technologies available.We also explore taste and odor investigations, disinfection byproducts, and volatile organic compounds, plus the surprising reality of why regulated labs move slowly when adopting new instrumentation. You'll learn about the quality control checkpoints, peer review processes, and the misconceptions surrounding analytical turnaround times in compliance labs.<h5>Topics Covered:</h5><ul><li>Role of organic chemistry in regulated drinking water labs</li><li>EPA compliance requirements and regulatory bodies (EPA, PA-DEP)</li><li>PFAS detection using Method 537.1 and LC-MS</li><li>The critical importance of nitrogen blowdown sample concentration</li><li>Taste and odor analysis: MIB, Geosmin, and unknown compound identification</li><li>Why regulated methods evolve slowly (validation timelines, approval processes)</li><li>Quality control procedures: calibration checks, matrix spikes, surrogate standards, internal standards</li><li>Automated sample preparation and lab efficiency</li><li>Future PFAS regulations and Method 533 expansion</li></ul><h5>Ideal For:</h5><ul><li>Analytical chemists and environmental lab professionals</li><li>Water utilities and compliance officers</li><li>Chromatography practitioners interested in regulated workflows</li><li>Anyone curious about how drinking water safety is ensured</li></ul><h2>Video Transcription</h2><h3>Ensuring Safe Drinking Water Through Advanced Analytical Chemistry</h3><h4>Insights from a Regulated Water Testing Laboratory</h4>Analytical laboratories responsible for regulated drinking water testing operate under strict compliance frameworks to ensure the delivery of safe and reliable water supplies. In this interview, Alex, an organic chemist at Aqua America, outlines the scope of analytical work conducted in a modern water quality laboratory. The team primarily focuses on the determination of taste- and odor-causing compounds, disinfection byproducts, volatile organic compounds (VOCs), and per- and polyfluoroalkyl substances (PFAS). These analyses rely heavily on GC-MS and LC-MS instrumentation, supported by rigorous maintenance programs to ensure continuous operational performance and data reliability.<h4>Regulatory Compliance and Quality Control in Drinking Water Analysis</h4>Operating as a regulated drinking water laboratory requires adherence to stringent requirements established by agencies such as the U.S. Environmental Protection Agency (EPA) and state-level regulatory bodies. Compliance is driven by extensive quality control protocols integrated into every analytical batch. Typical workflows include calibration verification, matrix spike recovery assessments, internal standard monitoring, and surrogate performance checks. Notably, analytical batches are often limited in sample number to accommodate a substantial proportion of quality control samples, reflecting the critical importance of data defensibility in regulatory reporting.One common misconception is the perceived speed at which results can be delivered. In reality, comprehensive sample preparation, including extraction procedures and validation steps, can extend turnaround times to a full working day or longer. Additionally, validated regulatory workflows impose limitations on the rapid adoption of new analytical technologies, as method modifications must undergo formal evaluation and approval before implementation.<h4>Analytical Strategies for Taste and Odor Investigations</h4>Taste and odor events represent a significant operational challenge for water utilities. Standard targeted methods are routinely applied for compounds such as 2-methylisoborneol (MIB) and geosmin, which are commonly associated with earthy or musty sensory characteristics. When targeted analysis does not reveal the source, laboratories employ broad-scan GC-MS screening combined with spectral library interpretation to identify potential causative compounds. In some cases, sensory evaluation panels complement instrumental analysis, providing preliminary insight into potential treatment-related or environmental influences affecting water quality.<h4>PFAS Monitoring: Methodological Complexity and Trace-Level Sensitivity</h4>PFAS determination represents a rapidly evolving priority in drinking water monitoring. The laboratory currently applies EPA Method 537.1, with efforts underway to expand capabilities through certification for Method 533, thereby broadening analyte coverage. Analytical workflows typically involve solid-phase extraction followed by solvent evaporation using nitrogen-assisted blow-down techniques to achieve the trace-level sensitivity required for regulatory compliance. This concentration step is essential because PFAS compounds remain non-volatile under controlled evaporation conditions, enabling enhanced detection performance upon reconstitution and LC-MS analysis.<h4>Future Directions in Drinking Water Analytics</h4>Looking ahead, the primary technological driver in regulated water analysis is the demand for increasingly lower detection limits and expanded compound coverage. While regulatory frameworks can slow methodological innovation, laboratories continue to pursue efficiency improvements, such as automated sample preparation systems and optimized analytical workflows. These advances support the growing need to process high sample volumes while maintaining the stringent data quality standards required for public health protection.Ultimately, the work performed in regulated drinking water laboratories represents a critical intersection of analytical chemistry, environmental monitoring, and public safety. Continuous methodological refinement, coupled with advances in mass spectrometry and sample preparation technologies, will play a central role in addressing emerging contaminants and ensuring long-term water quality assurance.<blockquote>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.</blockquote><blockquote><h4>Concentrating on Chromatography Podcast</h4>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!You can find Concentrating on Chromatography Podcast in podcast apps:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://open.spotify.com/show/1wZg67rCjoGju4yhqxI3tL">Spotify</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://podcasts.apple.com/tz/podcast/concentrating-on-chromatography/id1788429185">Apple podcast</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://podscan.fm/podcasts/concentrating-on-chromatography">podscan</a></li></ul>and on <a target="_blank" rel="noopener noreferrer" href="https://www.youtube.com/@ChromatographyTalk/videos">YouTube channel</a></blockquote>

Regulated Drinking Water Testing: PFAS Detection, Sample Prep & Real Lab Insights

Anna Vanluchene&nbsp;from UCT Prague’s&nbsp;Department of Chemical Engineering has received a&nbsp;prestigious start-up grant from the Dagmar Procházková Fund. However, she did not receive funding right away. In this interview, she describes how she developed ten versions of her&nbsp;Illuminating Flow&nbsp;project idea (combining photocatalysis with flow reactors for pharmaceutical synthesis). She explains why she considers perseverance to be crucial when applying for grants, how international experience has influenced her approach to team management, and how her research can reduce the chemical industry’s&nbsp;dependence on fossil fuels and imports from China.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_2_5b7d63b8e9.jpg" alt="VŠCHT Prague/Tomáš Balický: I waited two years for a start-up grant and wrote ten versions of my project idea" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_2_5b7d63b8e9.jpg 127w," sizes="100vw" width="1128" height="1387"><h5>What did the Dagmar Procházková Fund grant mean to you?</h5>I&nbsp;consider it to be a&nbsp;great success. It is the first injection of funding that will allow me to ensure full independence for my research endeavour, to start my own research group, and to fund students so I&nbsp;can get started properly.<h5>What have been your previous experiences with grants?</h5>During my doctorate, a cotutelle (international doctorate under dual supervision), I&nbsp;was funded by a&nbsp;grant from the French government. Then I&nbsp;worked at the Academy of Sciences of the Czech Republic (CAS) and received a&nbsp;Marie Skłodowska-Curie Action (MSCA) Postdoctoral Fellowship to go abroad. The idea for my now-funded project was developed about two years ago and, since then, I&nbsp;have gradually developed and adapted the idea for various grant calls. I&nbsp;submitted about ten different versions of the proposal. I&nbsp;did not receive a&nbsp;grant from the Dagmar Procházková Fund last year, but this year, my application was successful.<h5>This probably requires a&nbsp;great deal of patience and perseverance.</h5>Certainly, because the success rates for most grants have been declining for some time. But as a&nbsp;motivational example, I&nbsp;will tell the story of Timothy Noel, a&nbsp;Belgian professor of chemistry living in the Netherlands. He applied for the prestigious European Research Council (ERC) grant, which is among the most sought-after in Europe, seven times. But no failure deterred him and eventually he succeeded and opened the door to potentially massive grant funding. He was already one of the world’s&nbsp;top scientists in the field at that time and openly described his journey on his blog <a target="_blank" rel="noopener noreferrer" href="https://www.noelresearchgroup.com/2022/03/17/my-personal-story-to-obtain-an-erc-grant-7-submissions-4-interviews-and-6-heartbreaks/">blog</a>.<h5>What advice does this convey to other grant applicants and early career researchers?</h5>Start early, read a&nbsp;lot, don’t&nbsp;give up, and—most importantly—apply repeatedly. Learn from rejections and overcome possible frustration from failures. Read blogs and books by successful people, where you will find not only the glorious results of their work, but also the hardships they faced over their entire journeys. Of course, building your team and laboratory is impossible without finances. I&nbsp;myself still hope that I&nbsp;will be able to receive even bigger grants in the future.<h5>How has your international experience influenced your scientific approach?</h5>A&nbsp;lot and on several levels. Different laboratories teach you how to do&nbsp;things differently. You gain varied experience about how different institutions function. You see other people’s&nbsp;positive motivations, their ability to be ambitious without negativity, their involvement in institutional matters, their openness to cooperation with companies (e.g., tech transfers, spin-offs). The most important thing is to broaden your horizons. I&nbsp;see going abroad as a&nbsp;necessity. What I&nbsp;have taken away the most is drive, great support, and the idea that scientific output is not just about metrics, but also about dedication to one’s&nbsp;topic.<h5>What is your Illuminating Flow: Transport Phenomena in Photocatalysis about, in layperson’s&nbsp;terms, and how is it unique?</h5>Most of today’s&nbsp;chemical industry is still based on thermal processes and fossil fuels. Photochemistry enables electrification, where the energy source is photons delivered by LEDs, which can generate electricity from renewable sources. Current research focuses mainly on chemical reactions and their mechanisms, but as a&nbsp;chemical engineer, I&nbsp;focus on designing processes and reactors suitable for industrial use. In batch reactors, light fades rapidly with distance from a&nbsp;source, so much of a&nbsp;reaction mixture is not illuminated. Flow reactors solve this problem, but they bring new challenges such as working with solid catalysts and subsequently scaling up production and achieving higher production rates of the desired chemicals at a&nbsp;given scale.One can imagine a&nbsp;transparent tube with a&nbsp;catalyst on the walls, upon which light shines and through which reactants flow. This project has a&nbsp;unique emphasis on engineering solutions and overall process efficiency.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_3_b978abf25c.jpg" alt="VŠCHT Prague/Tomáš Balický: I waited two years for a start-up grant and wrote ten versions of my project idea" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_3_b978abf25c.jpg 241w," sizes="100vw" width="1228" height="799"><h5>So, were you inspired by a&nbsp;gap in the market to connect photocatalysis with transport phenomena?</h5>Exactly. I&nbsp;combine my areas of expertise: microfluidics, photocatalytic degradation of organic substances (CAS), and synthesis (MSCA Postdoctoral Fellowship). The idea itself is not new, and pharmaceutical companies are very interested in “greener” photochemistry, but in practice, there is often a&nbsp;lack of appropriate engineering solutions and apparatus for industrial use.<h5>What are the practical applications of your work and what substances are you focusing on?</h5>Mainly on pharmaceuticals and on the synthesis of so-called fine chemicals, which are often the building blocks for the production of pharmaceuticals. There is also a&nbsp;geopolitical dimension to this, i.e. less dependence on imports from China and sustainable synthesis in Europe where it makes economic sense.<h5>And what chemicals are you specifically talking about?</h5>For example, building blocks for advanced synthesis, compounds prepared by trifluoromethylation reactions, or products of oxidation reactions with singlet oxygen. At the same time, we focus on reactions that are, in the classical design process, less safe or technologically demanding, where new approaches, such as photochemistry in flow reactors, could be safer and have better process control. Of course, this is not a&nbsp;universal solution for all types of reactions.<h5>The goal of this project?</h5>I&nbsp;plan to start a&nbsp;fully functional laboratory and research team, create high-quality experimental data on selected molecules and based on them, try to build cooperation with industrial partners. Without data, it is impossible to come to companies with just an idea. Within three years, I&nbsp;would like to have results that can be realistically presented and further developed.<h5>What are the main challenges in transport phenomena during photocatalysis?</h5>The methodology for repeatability of experiments in photochemistry is relatively demanding and there are unforeseen obstacles in building apparatus. Also, the scale-up from microliters to a&nbsp;larger scale.<h5>What methodology will you use, and how big are the microreactors and their flow rates?</h5>I&nbsp;have two different directions in methodological design. The first direction involves microreactors the size of a&nbsp;laboratory slide. You make a&nbsp;structure using a&nbsp;laser, and then you have to cast it and make a&nbsp;microreactor. This allows you to quickly adjust the geometry of the reactor. This method is, of course, not applicable in the commercial setting, but it is ideal for studying transport phenomena and precise measurements.The second direction involves reactors that are flow cells. These are already larger, approximately 15 x 15 centimetres, and their flow rates are in the order of millilitres per hour. This is the initial scale that we will further increase during the project.<h5>There is a&nbsp;big difference between a&nbsp;flow rate of microlitres per hour and industrial needs. Will it not work differently in reality?</h5>Our research will focus on studying the phenomena themselves for now, and scaling will be addressed later. In addition, we will combine the experimental data obtained with computer simulations that will help design suitable conditions for a&nbsp;larger scale. For some high-value fine chemicals, these scales, combined with continuous operation or parallelization of reactors, may already be practically usable.<h5>What catalysts will you use and how will you attach them to the reactor walls?</h5>I&nbsp;am focusing on heterogeneous photocatalysis, and we will mainly use graphitic carbon nitride and its more advanced modifications. These are semiconductor materials that can be synthesized relatively easily and are suitable for immobilization on glass reactor walls. A&nbsp;key part of this project is the creation of a&nbsp;stable catalytic layer for long-term flow-through operations. To increase the contact of reactants with the catalyst, we will also consider multiphase modes, for example, gas bubbling, in order to disrupt the otherwise laminar flow.<h5>Why did you choose this field and the Department of Chemical Engineering?</h5>During my postdoc in Belgium, the department had an opening for an Assistant Professor position that caught my attention and I&nbsp;applied for it. I&nbsp;did my undergraduate, graduate, and initial doctoral studies here, and I&nbsp;love the department. I&nbsp;have a&nbsp;Bachelor’s&nbsp;degree in Chemistry.<h5>Are you collaborating with anyone?</h5>We collaborate with BUT Brno focusing on creating layers and immobilizing catalysts on glass, as well as with the Institute of Chemical Process Fundamentals of the Academy of Sciences of the Czech Republic. And as for organic synthesis, we are connected with Ghent University via postdoc internships. At the same time, my colleague Viola Tokárová and I&nbsp;received a&nbsp;Czech Science Foundation grant in cooperation with BUT Brno and Masaryk University, with our part of the project focusing on the use of flow reactors for photochemical reactions and testing the antibacterial properties of photocatalytic materials. And I&nbsp;am writing other grant proposals in which I&nbsp;am trying to build new collaborations.<h5>What does the creation of an independent research group at UCT Prague look like?</h5>I&nbsp;started by renovating the premises that were assigned to me and gradually building my team. It is important for research work to have Ph.D. students; I&nbsp;have already hired one and we will recruit more. In addition to building the group, I&nbsp;will engage in securing further funding for the group, so I&nbsp;will be writing more grant proposals. It is important to think far enough in advance when it comes to prospective funding for a&nbsp;research group.<h5>What type of students are you looking for?</h5>The laboratory and team I&nbsp;are building will be very multidisciplinary, just like the area I&nbsp;am working on. That is why I&nbsp;am looking for students who are attracted to true multidisciplinary research, those who, for example, have knowledge of engineering, but who don’t&nbsp;mind a&nbsp;little bit of pure chemistry. One student in their own right does not have to (and cannot) know every subject, so I&nbsp;will ideally have a&nbsp;team consisting of different people with different research backgrounds. Motivated, DIY-type students who would rather enthusiastically build or invent something themselves than conduct repetitive measurements. Organic or analytical chemists will also find their place here. If this topic is interesting to students in any way, they can definitely contact me. I&nbsp;am also open to interdepartmental cooperation with other UCT Prague Faculties.<h5>How would you describe your path to photocatalysis/chemical engineering?</h5>Studying Chemistry as an undergrad gave me a&nbsp;broad perspective, but I&nbsp;was gradually narrowing my focus and eventually chose engineering. Chemical engineering intrigued me with its logic and was the easiest for me to grasp at the time. But I&nbsp;have always enjoyed working on projects more than the studies themselves. Even during my Bachelor studies, I&nbsp;really enjoyed and was interested in the Professor Štěpánek Group’s&nbsp;projects, where I&nbsp;was doing something completely different than I&nbsp;do&nbsp;now. I&nbsp;only got into photochemistry during my time at CAS and then, during my postdoctoral fellowship, I&nbsp;devoted myself to electrochemistry. My current focus is, thus, a&nbsp;natural interlinking of all these areas. Consequentially, I&nbsp;developed an awareness of the necessity to become independent and return to the department with my own, different research agenda, which, in my opinion, is an important and correct basis for establishing my own research group.<h5>What is the biggest challenge of this project for you?</h5>The transition from being a&nbsp;postdoc to a&nbsp;leadership position is a&nbsp;big change for me and I&nbsp;think it is not talked about enough. It means a&nbsp;shift from my own experimental work to leading a&nbsp;team, planning and delegating tasks, and motivating students. From a&nbsp;practical point of view, one of the main challenges is the transfer of reactions from the microscale to functional systems, the construction of reactors, the immobilization of catalysts, and generally confirming that this direction makes sense in the long term and that it has future potential.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_1_66ac267e06.jpg" alt="VŠCHT Prague/Tomáš Balický: I waited two years for a start-up grant and wrote ten versions of my project idea" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_VSCHT_Praha_Na_startovaci_grant_jsem_cekala_dva_roky_a_napsala_deset_verzi_projektu_1_66ac267e06.jpg 155w," sizes="100vw" width="830" height="839">

I waited two years for a start-up grant and wrote ten versions of my project idea

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The University of Chemistry and Technology, Prague is a natural centre of first-rate study and research in the area of chemistry in Czechia and is one of the country's largest educational and research institutions focused on technical chemistry, chemical and biochemical technologies, material and chemical engineering, food chemistry, and environmental studies.

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Organomation, founded in 1959, designs and manufactures high-quality nitrogen evaporators and extraction systems. Known for innovation and durability, their lab instruments are used globally for efficient sample preparation with strong customer support.

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EST Analytical FLEX 2 Robotic Sampling Platform

The FLEX 2 autosampler streamlines GC/GC-MS workflows with liquid, headspace, and SPME capability, MTX tool change, and Prep Ahead for faster, more reliable VOC analysis.

The FLEX 2 is a versatile GC autosampler designed to handle both sample preparation and sample introduction for GC and GC/MS analysis. Supporting liquid injection, headspace, and SPME, it delivers exceptional accuracy and reproducibility. Its Prep Ahead function improves efficiency by allowing sample preparation during ongoing GC runs, maximizing system utilization and throughput.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/EST_Analytical_FLEX_2_Robotic_Sampling_Platform_3_853e02f151.jpg" alt="EST Analytical: FLEX 2 Robotic Sampling Platform" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_EST_Analytical_FLEX_2_Robotic_Sampling_Platform_3_853e02f151.jpg 168w," sizes="100vw" width="628" height="584"><h4>Key Features</h4><h5>Flexible Sample Preparation with Multi Tool Change (MTX)</h5><ul><li>Automated Multi Tool Change (MTX) enables seamless switching between tools</li><li>Enhances laboratory productivity, accuracy, and safety by reducing manual prep errors</li><li>Supports dilution, reagent addition, and internal standard spiking with precision</li><li>Can operate as a benchtop preparation station for derivatization and extraction steps</li></ul><h5>Liquid Injection Capabilities</h5><ul><li>Injection range: 0.5–10 μL (standard syringe) or 50–500 μL (optional large-volume syringe)</li><li>Supports both standard and large-volume injections (up to 500 μL)</li><li>Programmable injection speed control, from ultra-fast to very slow</li><li>Optional cooled trays available for temperature-sensitive samples</li></ul><h5>Headspace Sampling</h5><ul><li>Injection range: 100–2500 μL (2.5 mL syringe), 100–1000 μL (1.0 mL syringe), or 500–5000 μL (5.0 mL syringe)</li><li>Offers both orbital and oscillating agitation to improve sample consistency</li><li>Six heated vial positions for 2, 10, or 20 mL vials</li><li>Temperature range: ambient to 200 °C</li><li>Shaking: orbital (120–750 rpm) or oscillation (190 Hz)</li></ul><h5>Automated SPME</h5><ul><li>Compatible with both traditional and direct immersion SPME methods</li><li>Heated conditioning station:<ul><li>Fiber: ambient to 350 °C</li><li>Needle: ambient to 150 °C</li><li>Sweep gas port for conditioning</li></ul></li><li>Heated mixing station: ambient to 150 °C, mixing speeds 380–725 rpm</li></ul><h5>Efficiency &amp; Throughput</h5><ul><li>Prep Ahead function allows ongoing sample prep during GC runs</li><li>Fully automates switching between liquid injection, headspace, and SPME with MTX</li><li>Reduces manual workload and preparation errors while improving reproducibility</li></ul><h4>Technical Specifications</h4><ul><li>Compatible Systems: GC and GC/MS platforms</li><li>Injection Modes: Liquid (0.5–500 μL), Headspace (100–5000 μL), SPME (traditional &amp; direct immersion)</li><li>Temperature Ranges: Headspace up to 200 °C, SPME fiber up to 350 °C, SPME needle up to 150 °C</li><li>Agitation: Orbital (120–750 rpm) and oscillating (190 Hz)</li><li>Capacity: Six heated vial positions for 2, 10, or 20 mL vials</li><li>Automation: Multi Tool Change (MTX), Prep Ahead function</li></ul>

EST Analytical LGX-50 for Methane in Water

The EST LGX-50 automates RSK-175 dissolved gas testing in water, boosting throughput, ensuring ASTM/EPA compliance, and reducing manual sample preparation errors.

The LGX-50 automates the preparation of water samples for headspace analysis of dissolved gases such as methane, ethane, and ethene. Traditionally, RSK-175 testing has been labor-intensive and time-consuming, requiring manual vial preparation. The LGX-50 eliminates this step, streamlining workflows and ensuring compliance with EPA Method 5035 and ASTM D8028. By automating dissolved gas extraction, laboratories can boost throughput, reduce errors, and deliver more consistent results for shale gas and environmental testing.<h4>Key Features</h4><h5>Maximized Productivity</h5><ul><li>Fully automates RSK-175 sample processing</li><li>ASTM D8028 compliant for dissolved gas testing</li><li>Holds up to 50 samples for high-throughput operation</li><li>Optical sensors prevent vial misplacement and syringe/elevator errors</li><li>Robust XYZ design ensures reliability and consistent performance</li></ul><h5>Simplified Operation</h5><ul><li>Intuitive, user-friendly software designed for quick setup and operation</li><li>Remote access functionality allows labs to monitor sample progress via the server</li><li>Reduces manual preparation steps, increasing accuracy and reproducibility</li></ul><h4>Technical Specifications</h4><ul><li>Compliance: EPA Method 5035, ASTM D8028</li><li>Capacity: Up to 50 samples per batch</li><li>Target Compounds: Methane, ethane, ethene, and other dissolved gases in water</li><li>Automation: XYZ robotic design with optical sensors for error prevention</li><li>Software: Intuitive, remote-access capable interface</li></ul>

Watrex Helium Saver – intelligent helium savings for GC/MS

Helium Saver™ by Watrex Praha cuts helium use in GC/MS. It auto-switches to nitrogen when idle, prevents manual errors, and lowers costs without sacrificing analytical quality.

An automated device that significantly reduces helium consumption in gas chromatography. It switches between helium and nitrogen according to the set schedule, eliminates errors from manual switching, and lowers operating costs – without compromising measurement quality. Easy configuration via USB, universally compatible with any GC/MS system.&nbsp;Helium Saver™ by <a target="_blank" rel="noopener noreferrer" href="https://watrex.com/?utm_source=labrulez&amp;utm_medium=propagace&amp;utm_campaign=labrulez_produkty">Watrex Praha</a> is an innovative device designed for gas chromatography (GC) and GC/MS systems, providing an efficient answer to the rising costs of helium. Helium is indispensable for GC/MS thanks to its inertness and separation properties, but it is scarce, expensive, and its price continues to increase.&nbsp;<h4>How does Helium Saver™ work?&nbsp;</h4>The device automatically switches between helium and nitrogen according to a user-defined schedule:&nbsp;<ul><li>during measurements, helium is used,&nbsp;</li><li>outside of working hours (e.g., overnight), the system runs on nitrogen,&nbsp;</li><li>before the start of the working day, the chromatograph is automatically flushed with helium, ensuring it is ready for analysis.&nbsp;</li></ul>This process eliminates the need for manual switching, reduces human error, and significantly lowers helium consumption.&nbsp;<h4>Key Benefits&nbsp;</h4><ul><li>Helium and cost savings&nbsp;– consumption of helium reduced by tens of percent.</li><li>No compromise in measurement quality&nbsp;– analyses are always performed under optimal conditions.&nbsp;</li><li>Easy USB configuration&nbsp;– the device connects as a flash drive, settings can be edited in any text editor, no special software required.&nbsp;</li><li>Universal compatibility&nbsp;– easily integrates with any GC/MS system.&nbsp;</li><li>Automatic and manual modes&nbsp;– flexible operation depending on laboratory needs.&nbsp;</li><li>Multi-instrument support&nbsp;– can be configured for multiple gas chromatographs simultaneously.&nbsp;</li></ul><h4>Why choose Helium Saver™?&nbsp;</h4>Helium Saver™ is the ideal choice for laboratories aiming to cut operating costs, increase efficiency, and contribute to more sustainable use of helium – a limited natural resource. The device combines user-friendly operation with intelligent automation, offering a modern solution for everyday laboratory practice.

ARC Polyarc System

A Breakthrough Innovation Revolutionizing GC/FID Technology. The Polyarc System is transforming the way scientists use gas chromatographs with Flame Ionization Detectors.

The Polyarc system has a catalytic microreactor that enhances new and existing gas chromatographs (GCs) with flame ionization detectors (FIDs) by converting all organic compounds to methane molecules prior to their detection by the FID. In doing so, the Polyarc system reduces the need to perform time-consuming calibrations by creating a uniform detector response for truly universal carbon detection.
The Polyarc system gives scientists the capability to determine purity, quantify unknowns, qualify products, investigate, improve development and more in a simple, fast and more economical way that is transforming the industry.
<blockquote>
Available for gas chromatographs (GC) <a href="https://gcms.labrulez.com/products?category=1&amp;manufacturerItems=10">Agilent</a> 5890, 6890, 7820, 7890, 8890, <a href="https://gcms.labrulez.com/products?category=1&amp;manufacturerItems=1">Shimadzu</a> 2030, <a href="https://gcms.labrulez.com/products?category=1&amp;manufacturerItems=3">Thermo Fisher</a>, Varian, Bruker a Scion GC.
</blockquote>
<h3>What is Polyarc?</h3>
The Polyarc is the next evolution of flame ionization detection (FID). The Polyarc converts the FID into a truly universal carbon detector using proprietary catalytic reactions that convert organic molecules to methane immediately prior to detection.
<h3>Why is it important?</h3>
The FID has two main challenges: lack of uniform response and low response to certain compounds. The Polyarc enhances your FID to solve these challenges by giving your FID a uniform response to nearly all organic molecules. The result is more accurate data, improved productivity, lab efficiencies, and the ability to detect more compounds.
<h3>How Does the Polyarc® System Work to Simplify and Improve GC/FID Quantification?</h3>
The Polyarc system has a catalytic microreactor that enhances GC/FIDs by converting all organic compounds to methane molecules prior to detection by the FID. The result?
A universal response for ALL organic molecules.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Polyarc_FID_vs_FID_Response_Factors_0f9c958558/ARC-PolyarcFID-vs-FID-Response-Factors.jpg" alt="ARC: Comaprison of Polyarc/FID vs FID Response Factors.jpg"/>
<h3>The Polyarc System Features an Optimized Design and Seamless Integration</h3>
The Polyarc system is the first commercial technology of its kind. The device uses proprietary technologies including novel catalysts, a specially designed 3D-printed micro reactor, and fast seamless integration into existing equipment.
The optimized internal design and catalyst microstructure maintains separation performance and peak shape while increasing sensitivity and enabling accurate quantification without calibration standards.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Optimalizovany_design_a_specialne_navrzeny_3_D_tisteny_mikroreaktor_Polyarc_70ccedc41e/ARC-Optimalizovany-design-a-specialne-navrzeny-3D-tisteny-mikroreaktor-Polyarc.jpg" alt="ARC: Specially designed 3D-printed micro reactor Polyarc"/>
<h3>Perform Cutting-Edge Chromatography on Any Organic Compound with a Polyarc® System</h3>
Realize a greater breadth of analysis with improved detection of compounds previously invisible or with an extremely low sensitivity by gas chromatography using FID only — while reducing the need for time intensive calibration.
The careful selection and robust catalyst design enables the analysis of a wide variety of compounds including a range of heteroatoms, compounds of various sizes, and samples containing common catalytic poisons (e.g., S).
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Analyza_siroke_skaly_sloucenin_pomoci_Polyarc_systemu_3e18241358/ARC-Analyza-siroke-skaly-sloucenin-pomoci-Polyarc-systemu.png" alt="ARC: Polyarc system enables the analysis of a wide variety of compounds"/>
<h3>How Does the Polyarc System Compare to a Methanizer?</h3>
A conventional methanizer converts CO and CO₂ to methane, allowing low level FID detection of CO and CO₂. The significant advantage of the Polyarc system is that it converts all compounds to methane, allowing not only for the detection of CO and CO₂ , but also millions of other organic compounds.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Srovnani_systemu_Polyarc_s_metanizerem_7df16e09c7/ARC-Srovnani-systemu-Polyarc-s-metanizerem.jpg" alt="ARC: Comparison of the Polyarc System with a metanizer"/>

ARC Jetanizer (Methanizer)

The Jetanizer is the easiest and most robust methanizer.

<h3>What is Jetanizer™?</h3>
The Jetanizer is the easiest and most robust methanizer. A methanizer is a chemical reactor that converts carbon dioxide and carbon monoxide to methane to enable sensitive detection by a flame ionization detector (FID) from &lt;20 ppb to 100%!
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Analyza_CO_2_od_1ppm_do_100_s_pouzitim_GC_jetanizeru_FID_9c922be2e9/ARC-Analyza-CO2-od-1ppm-do-100percent-s-pouzitim-GC-jetanizeru-FID.jpg" alt="ARC: CO₂ analysis from 1ppm to 100% with GC/Jetanizer/FID"/>
<h3>Why is it important?</h3>
<h4>Low-level detection of CO and CO₂ is important in:</h4>
<ul>
<li>catalysis </li>
<li>hydrogen (H₂) purity analysis </li>
<li>dissolved gas analysis (DGA)</li>
<li>greenhouse gas (GHG) analysis, </li>
<li>transformer oil gas analysis (TOGA)</li>
<li>ethylene/propylene monomers analysis </li>
<li>safe entry analysis, and more</li>
</ul>
Traditionally, large nickel-catalyst-filled tube methanizers are used, however, they are prone to frequent failures, and they are difficult and time consuming to operate and maintain. 
<blockquote>
Legacy nickel catalyst methanizers take 2-6 hours to install and replace. Jetanizers take &lt;5 minutes.
</blockquote>
ARC’s Jetanizer solves these challenges by improving response, robustness and ease of installation, by incorporating state-of-the-art catalysts into an FID jet. Moreover, the Jetanizer enables low level &lt;1 ppm formaldehyde analysis by GC avoiding the pitfalls of HPLC analysis of formaldehyde.
<blockquote>
For use with these GC models: <a href="https://gcms.labrulez.com/products?category=1&amp;manufacturerItems=10">Agilent 5890, 6890, 7890, 8890, Intuvo</a>, <a href="https://gcms.labrulez.com/products?category=1&amp;manufacturerItems=1">Shimadzu 2010, 2030 GC</a>.
</blockquote>
<h3>Benefits over Traditional Methanizers</h3>
<ul>
<li>Lower up-front cost</li>
<li>No extra plumbing: minimize fittings and leaks</li>
<li>No extra heater or controller: utilizes heat from FID</li>
<li>FAST installation: Less than 5 minutes</li>
<li>Ability to be used with formaldehyde</li>
<li>Higher sulfur tolerance</li>
<li>Higher catalytic activity = larger linear dynamic range</li>
<li>Free up space on the GC</li>
<li>No toxic metals: The Jetanizer™ does not contain nickel catalysts</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Kalibrace_analyzy_CO_2_s_pouzitim_GC_jetanizeru_FID_2f0b6171fc/ARC-Kalibrace-analyzy-CO2-s-pouzitim-GC-jetanizeru-FID.jpg" alt="ARC: CO₂ analysis calibration with GC/Jetanizer/FID"/>

ARC Precision Split

ARC’s PrecisionSplit device allows scientists and chromatographers to take advantage of the quantitative power of the Polyarc/FID in combination with the mass identification power of the mass spectrometer, all in the same injection in real time.

<h3>Why does my MS need an FID?</h3>
A mass spectrometer (MS) provides valuable qualitative data, but poses several challenges to accurate quantification. Adding a flame ionization detector (FID) in parallel with the MS gives complementary quantitative carbon concentrations with minimal extra effort or equipment. We believe every MS needs an FID companion for quantitative analysis, especially for non-targeted analysis or tentatively identified compounds where quantification is desired.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Precision_Split_6271ed1240/ARC-Precision-Split.jpg" alt="ARC: Precision Split"/>
<h3>The benefits of a MS/FID split:</h3>
<ul>
<li>Virtually eliminate response factor variability</li>
<li>Quantify accurately (better linearity, more consistent response, fewer calibration errors)</li>
<li>Improve sensitivity for poor ionizers with the FID</li>
<li>Save your source!</li>
</ul>
<h3>The Data</h3>
Response factor (RF) variation in the mass spectrometer (i.e., the relative response of the MS to different chemicals) can lead to significant errors in quantification. Two compounds that have the same response/area in the MS can have concentrations that differ more than 100-fold (see <a href="https://www.sciencedirect.com/science/article/pii/S0731708520304283">Jordi et al.</a>). 
As you can see below, the Polyarc/FID split can reduce this response factor variation so that accurate quantification of tentatively identified compounds is possible.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Variance_RF_u_MS_detektoru_8e02773edc/ARC-Variance-RF-u-MS-detektoru.jpg" alt="ARC: RF variation with MS"/>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Variance_RF_s_Polyarc_FID_splittrem_ca7def3cb3/ARC-Variance-RF-s-Polyarc-FID-splittrem.jpg" alt="ARC: RF variation with Polyarc/FID split"/>

ARC ISOTOPE (COMBUSTION REACTOR FOR IRMS)

The World’s First Low Temperature Combustion Reactor for GCC-IRMS

Winner of <a href="https://theanalyticalscientist.com/techniques-tools/tasias-2018-strokes-of-genius">The Analytical Scientist Innovation Awards in 2018</a>, the ARC Isotope was developed for low-temperature combustion of steroids and hydrocarbons for carbon isotope measurements. 
The system easily integrates into existing instrumentation and outperforms conventional combustion reactors.
<h3>GCC-IRMS Chromatograms of steroids and alkanes using the ARC Isotope reactor show excellent performance and operability compared with legacy reactors.</h3>
<h4>Advantages Include:</h4>
<ul>
<li>Excellent Performance</li>
<li>Lower Operating Temperature</li>
<li>Reduced Complexity</li>
<li>Improved Robustness</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_GCC_IRMS_chromatogramy_steroidu_a_alkanu_s_pouzitim_reaktoru_ARC_ISOTOPE_d6299edd7a/ARC-GCC-IRMS-chromatogramy-steroidu-a-alkanu-s-pouzitim-reaktoru-ARC-ISOTOPE.jpg" alt="ARC: GCC-IRMS chromatograms of steroids and alkanes using ARC ISOTOPE reactor"/>
Data provided by Tobias, H.J., et al., Analytical Chemistry, <a href="https://pubs.acs.org/doi/10.1021/acs.analchem.8b05043">Read More</a>

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