ISC 2026 - Day 2

<h4><strong>What if you could compress 179 days of grueling laboratory workflow into just 14 hours?</strong></h4><p><strong>In this episode of ‪ChromatographyTalk‬, ‪Organomation‬ General Manager David Oliva sits down with analytical chemist Laura Penabad to discuss her groundbreaking new research in biocatalysis and high-throughput screening. Evolving engineered enzymes typically requires checking thousands of variants—a massive bottleneck when traditional Liquid Chromatography-Mass Spectrometry (LC-MS) runs take minutes per sample. Laura reveals how her team built a modular screening platform that shatters this limitation, running samples 128 times faster than standard methods without sacrificing analytical accuracy.</strong></p><p>Laura breaks down the "orchestra" of technologies making this possible, including coupling nanoliter droplet microfluidics with Cyclic Ion Mobility-Mass Spectrometry (cIM-MS) to separate complex chemical isomers in milliseconds. She also shares the chaotic but triumphant behind-the-scenes stories of her PhD journey—from presenting a "comically bad" early poster at ASMS to recruiting an undergraduate mechanical engineer to build custom automation software from scratch.</p><p>If you are an early-career researcher, a mass spec enthusiast, or curious about the future of synthetic biology and machine learning in chemistry, this episode is packed with invaluable intuition and advice.</p><h3><strong>Video Transcription</strong></h3><h4><strong>From Months to Hours: Droplet Ion Mobility–MS for Biocatalysis Screening</strong></h4><p><strong>High-throughput screening is central to directed enzyme evolution, but conventional analytical workflows can create a difficult compromise: extremely fast screens often provide limited structural information, while techniques such as LC-MS offer much richer chemical insight at the cost of throughput. In a recent interview, analytical chemist Laura described how her work with droplet-based cyclic ion mobility mass spectrometry is helping bridge that gap—providing rapid analysis while retaining the ability to distinguish structurally similar products.</strong></p><p>Her research grew from an initially modest proof of concept into a screening platform capable of analyzing a 96-well plate in roughly ten minutes. The resulting workflow was approximately <strong>128 times faster than a conventional three-minute LC-MS analysis</strong>, opening new possibilities for directed evolution campaigns in which thousands of enzyme variants need to be evaluated.</p><h4>Directed evolution needs better analytical screening</h4><p>Biocatalysis takes advantage of enzymes as highly selective catalysts capable of performing reactions under relatively mild conditions. Directed evolution extends those capabilities by deliberately modifying enzyme sequences, expressing large numbers of variants, screening their activity, and using the best-performing mutants as starting points for subsequent rounds of evolution.</p><p>The process can be repeated multiple times, progressively steering an enzyme toward improved activity, altered substrate specificity, or even chemistry that does not occur naturally.</p><p>But the effectiveness of directed evolution depends heavily on the screening step. The more variants that can be analyzed—and the more useful chemical information that can be collected for each one—the more effectively researchers can explore the enormous sequence space available to an enzyme.</p><p>For Laura, this created a clear analytical challenge: develop a screening platform that was substantially faster than conventional chromatographic analysis without sacrificing the structural discrimination needed for chemically similar products.</p><h4><strong>From an imperfect first experiment to a working platform</strong></h4><p>The project did not begin with a polished high-throughput workflow.</p><p>Laura recalled looking back at her <strong>2023 ASMS poster</strong>, where the early system was still working with standards rather than true isomeric samples. Droplet introduction was slow—around six seconds per droplet—and the signals were far from the ideal reproducible, square, flat-topped profiles expected from replicate droplets.</p><p>Nevertheless, simply producing a droplet signal represented an important first milestone.</p><p>The decisive change came when the project stopped being treated merely as a demonstration that droplet ion mobility–MS could work and instead became a deliberate effort to build a <strong>robust screening platform</strong>.</p><p>Laura approached the problem in modules. First came reliable droplet introduction. Then the ion mobility separation method. Quantification became another independent component. Matrix effects were introduced later, gradually making the system resemble the conditions expected with real screening samples.</p><p>Each layer was tested before another was added.</p><p>This stepwise strategy became one of the central principles of the project: rather than attempting to optimize the entire system simultaneously, individual components were developed, challenged, and then assembled into an increasingly realistic workflow.</p><h4><strong>Finding the middle ground between speed and structural information</strong></h4><p>One of the biggest analytical problems in high-throughput screening is distinguishing products with the same nominal or exact mass.</p><p>Constitutional isomers may contain the same atoms and therefore generate the same mass-to-charge ratio, while differing only in how functional groups are arranged within the molecular structure. Very rapid optical or mass-based screens may therefore struggle to distinguish them.</p><p>Traditional LC-MS can solve many of these problems through chromatographic separation, but a several-minute analysis rapidly becomes impractical when thousands of enzyme variants must be screened.</p><p>Ion mobility offered Laura’s team another option.</p><p>Rather than separating compounds on a chromatographic timescale, ion mobility can differentiate ions according to their gas-phase behavior on a much shorter timescale. In the workflow described in the interview, this created a useful compromise: not the kilohertz throughput possible with some simple screening technologies, but dramatically faster structural differentiation than conventional LC-MS.</p><p>The goal was therefore not simply to achieve the fastest possible screen, but to find a <strong>middle-throughput analytical regime with enough resolving power to answer chemically meaningful questions</strong>.</p><h4><strong>A 96-well plate in about ten minutes</strong></h4><p>That strategy eventually produced one of the most striking results of the project.</p><p>The droplet cyclic ion mobility–MS platform processed a <strong>96-well plate in roughly ten minutes</strong>, while maintaining quantitative results comparable with the conventional LC-MS workflow used for comparison. According to the interview, this represented an approximately <strong>128-fold increase in analysis speed relative to a three-minute LC-MS run</strong>.</p><p>Laura described the successful plate experiment less as a surprise than as confirmation that the modular development strategy had worked.</p><p>Before reaching that point, the workflow had already been challenged through a sequence of increasingly demanding experiments: droplet formation, ion mobility separation, calibration, matrix-containing calibration, and cross-testing analytes at different concentrations. By the time the complete plate was analyzed, each individual part of the analytical system had already been tested under progressively more realistic conditions.</p><h4><strong>What does that speed mean for directed evolution?</strong></h4><p>The impact becomes even clearer when the workflow is considered at the scale of an entire directed-evolution campaign.</p><p>Laura’s manuscript estimated that a <strong>five-round campaign involving 5,000 variants would require approximately 179 days using the conventional LC-MS workflow but only about 14 hours using the new platform</strong>.</p><p>Compressing months of analytical work into less than a day has consequences beyond laboratory productivity.</p><p>It allows researchers to screen more enzyme variants and therefore sample a larger portion of sequence space. But the resulting datasets may also become increasingly valuable for computational approaches.</p><p>Rather than retaining information only about the best-performing enzyme variant, researchers can preserve data describing variants that performed poorly as well as those that succeeded. When genotype and phenotype information remain linked through the well-plate workflow, these larger datasets can potentially provide richer input for machine-learning models designed to guide subsequent rounds of enzyme evolution.</p><p>Faster analysis therefore does more than accelerate an existing experiment—it can change the scale and design of the experiment itself.</p><h4><strong>Balancing ion mobility resolution and signal</strong></h4><p>Increasing cyclic ion mobility separation time can improve resolution, but it also introduces an important trade-off: additional passes can reduce signal.</p><p>Laura optimized this balance experimentally by continuously infusing mixtures containing both isomers and progressively adjusting the ion mobility conditions. After tuning parameters such as wave height and velocity, increasing the separation to <strong>three passes</strong> provided baseline resolution at the high analyte concentrations used during method development.</p><blockquote><p><strong>Concentration, however, also mattered.</strong></p></blockquote><p>At higher ion populations, space-charge effects could broaden peaks and reduce the baseline separation. This meant that the optimal number of passes could not be selected independently of the concentration range required by the final assay.</p><p>Her broader advice for optimization is therefore application-driven: decide first what the analytical method actually needs to accomplish.</p><p>More speed will almost always require sacrificing something—resolution, signal intensity, quantitative precision, or another performance parameter. The key is to identify which compromise the application can tolerate and then optimize the system around that requirement.</p><h4><strong>Solving droplet carryover with a practical compromise</strong></h4><p>Droplet-based workflows present their own engineering challenges, including carryover between neighboring samples.</p><p>In Laura’s system, analytes showed little tendency to partition into the fluorinated oil separating aqueous droplets within the Teflon tubing. The more troublesome carryover occurred closer to electrospray ionization, where a small amount of sample could remain associated with the interface and appear when the next droplet arrived.</p><p>Rather than adding excessive engineering complexity to an already elaborate platform, the researchers adopted a pragmatic solution: a <strong>sacrificial wash droplet</strong> between analytical samples.</p><p>It is an example of a recurring theme throughout the project. The objective was not to construct the theoretically most sophisticated droplet system, but to create a screening workflow that remained sufficiently robust, reproducible, and practical for large numbers of samples.</p><h4><strong>High-throughput analysis also requires high-throughput data processing</strong></h4><p>Accelerating the mass spectrometry experiment created another bottleneck: the data.</p><p>The instrument produced a continuous intensity-versus-time trace rather than a neatly organized well-plate dataset. With small experiments, Laura could manually identify individual droplets and process the results in spreadsheets. That approach quickly became unrealistic as sample numbers increased.</p><p>The solution emerged through collaboration with an undergraduate mentee, Aiden, who helped develop a dedicated software tool for processing the continuous traces.</p><p>Laura defined how the software should behave and how the analytical information should be organized, while Aiden developed the computational implementation. The workflow itself was subsequently adjusted to make automated data processing more reliable—for example, by introducing marker columns that allowed the software to recognize the end of each plate row.</p><p>The resulting tool can accept the acquired traces together with information about plate dimensions and replicates and automatically return parameters including <strong>peak identity, duration, and the corresponding well position</strong>. A later version also generated an automatically populated heat map.</p><p>The experience illustrates how improving analytical throughput often requires simultaneous development of instrumentation, experimental design, and informatics. Making the measurement faster is useful only if the resulting data can be processed at a comparable speed.</p><h4><strong>Mentoring became part of the scientific process</strong></h4><p>The software project also reflects another theme Laura emphasized throughout the interview: the value of mentoring.</p><p>Several younger researchers contributed directly to the development of the final platform. Laura described mentees not simply as additional hands in the laboratory but as scientists capable of proposing their own hypotheses and experimental ideas.</p><p>Working with undergraduate researchers also influenced the way she organized experiments.</p><p>Because their available laboratory time was limited, each task needed to have a clear purpose. That encouraged a more disciplined approach to experimental planning: instead of performing experiments simply because they could be done, the team had to ask which experiment would most efficiently answer the next important question.</p><p>In that sense, mentoring became another mechanism for improving the research itself.</p><h4><strong>The next step: continuous, automated screening</strong></h4><p>Despite the dramatic increase in analytical speed, the current workflow still includes manual operations such as loading tubing and connecting the sample stream to the mass spectrometer.</p><p>The next engineering challenge is therefore automation.</p><p>Laura described ongoing work using the <strong>Venturi effect</strong> to pull samples directly from wells into the droplet system. Building on previous work in the laboratory with 96-well plates, she has already tested this approach with as many as <strong>2,000 samples</strong>.</p><p>The long-term direction is clear: continuous and robust droplet generation, automated handling of thousands of samples, rapid ion mobility separation, mass spectrometric detection, and automated reconstruction of the resulting data into plate-based outputs.</p><p>Combining those elements could move the system closer to the type of large-scale screening required for increasingly ambitious biocatalysis campaigns.</p><h4><strong>Learning mass spectrometry one problem at a time</strong></h4><p>Laura also reflected on the broader experience of developing the platform during her PhD.</p><p>Ion mobility and mass spectrometry initially appeared intimidating, particularly because they combine concepts from analytical chemistry, physical chemistry, separations, instrumentation, and electrical engineering. What eventually changed was not simply learning more facts, but developing the ability to move repeatedly between theory and experiment.</p><p>An unexpected result sends the researcher back to the underlying theory. A better understanding suggests a modified experiment. That experiment creates another observation, gradually building intuition about how the system behaves.</p><p>Her advice to early-career scientists is therefore to accept that this process takes time.</p><p>Advanced analytical techniques may initially appear overwhelming, but understanding develops incrementally through repeated interaction between theory, experimentation, failure, and refinement. Equally important, she emphasized the role of the supportive ion mobility–mass spectrometry community in making a technically demanding field more approachable for young researchers.</p><p>From the first inconsistent droplets to a platform capable of processing thousands of samples, that iterative mindset ultimately shaped the entire project.</p><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>

Droplet Cyclic Ion Mobility Mass Spec: Compressing Months of Enzyme Screening Into Just 14 Hours

ISC 2026 - Day 3

Article

Events

Video

Scientists

Interview

The International Symposium on Chromatography (ISC) represents the oldest conference series focussing on separation science. ISC symposia have been organised since 1956 in each even year. ISC is internationally recognised as one of the premier meeting series for discussion of all modes of chromatography and separation science with a broad coverage of techniques and applications.

International Symposium on Chromatography - (ISC)

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.

Organomation

KNAUER AZURA MWD 2.1L Multiwavelength Detector

KNAUER AZURA® MWD 2.1L is an 8-channel UV/VIS detector with 190–700 nm coverage, LightGuide technology, high sensitivity, and upgradeability to a DAD system.

<p><strong>The KNAUER AZURA® MWD 2.1L is a sensitive 8-channel UV/VIS multiwavelength detector designed for analytical, semi-preparative, and preparative liquid chromatography. Combining excellent performance, user-friendly operation, and affordability, it provides a versatile solution for routine and advanced LC applications.</strong></p><p>The detector features a newly developed optical unit and intelligent temperature management to ensure maximum sensitivity with minimal baseline drift. Optional LightGuide flow cells based on total internal reflection technology maximize light throughput and minimize peak dispersion, resulting in an optimized signal-to-noise ratio. An optional fiber-optic adapter allows physical separation of the flow cell from the detector, increasing safety when handling hazardous, explosive, or toxic materials.</p><p>The <strong>AZURA® MWD 2.1L</strong> can also be upgraded to a full <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/2423"><strong>AZURA® DAD 2.1L diode array detector</strong></a>, protecting future investments and enabling greater analytical flexibility.</p><h3><strong>Key Features</strong></h3><ul><li>Sensitive <strong>8-channel UV/VIS multiwavelength detector</strong></li><li>Wavelength range<strong> from 190 to 700 nm</strong></li><li>Simultaneous monitoring of <strong>up to 8 digital channels</strong></li><li>LightGuide flow cell technology for improved sensitivity and signal-to-noise ratio</li><li>Intelligent temperature management for minimal baseline drift</li><li>Wide selection of analytical, semi-preparative, and preparative flow cells</li><li>Optional fiber-optic adapter for remote flow cell positioning</li><li>Internal holmium filter for wavelength verification</li><li>Integrated leak sensor</li><li>Front-access lamp replacement</li><li>Upgradeable to the AZURA® DAD 2.1L diode array detector</li><li>Compatible with <strong>ClarityChrom®, OpenLAB®, Chromeleon™, PurityChrom®</strong>, and <strong>Mobile Control</strong></li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detector type: </strong>Multiwavelength Detector (MWD)</li><li><strong>Digital channels: </strong>8</li><li><strong>Analog channels:</strong> 4</li><li><strong>Light source: </strong>Deuterium lamp with integrated GLP chip</li><li><strong>Wavelength range: </strong>190–700 nm</li><li><strong>Spectral resolution: </strong>&lt;10 nm (FWHM)</li><li><strong>Slit width: </strong>7.0 nm</li><li><strong>Wavelength accuracy: </strong>±1 nm</li><li><strong>Wavelength repeatability: </strong>±0.1 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±5 µAU at 254 nm</li><li><strong>Drift:</strong> 400 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>100 Hz via LAN</li><li>12.5 Hz via analog output</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Stainless-steel and bio-inert configurations available</li><li>Optional LightGuide total-reflection technology</li></ul><h4><strong>Control and Communication</strong></h4><ul><li>LAN (RJ-45)</li><li>USB service interface</li><li>Analog inputs and outputs</li><li>Mobile Control stand-alone operation</li><li>Full software integration with chromatography data systems</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp identification</li><li>Lamp operating hours</li><li>Lamp ignition count</li><li>Comprehensive GLP reporting</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply:</strong> 100–240 V, 50–60 Hz</li><li><strong>Power consumption: </strong>75 W</li><li><strong>Dimensions (W × H × D):</strong> 361 × 158 × 523 mm</li><li><strong>Weight:</strong> 12.2 kg</li></ul>

KNAUER AZURA VWD 2.1L Variable Wavelength Detector

Flexible UV/VIS detector with up to four wavelengths, conductivity, temperature, and optional pH monitoring. Ideal for HPLC, FPLC, and purification applications.

<p><strong>The KNAUER AZURA® VWD 2.1L is a versatile variable wavelength detector designed for analytical HPLC, FPLC, and purification applications. Combining UV/VIS detection with optional conductivity, temperature, and pH monitoring, it provides exceptional flexibility for a wide range of chromatographic workflows.</strong></p><p>The detector supports simultaneous monitoring of up to four UV/VIS wavelengths across a broad spectral range from 190 to 900 nm. When equipped with KNAUER’s patented <strong>CombiLight flow cell</strong>, it can simultaneously measure UV absorbance, conductivity, and eluent temperature. An optional pH electrode further extends functionality by enabling real-time pH monitoring during chromatographic separations.</p><h3><strong>Key Features</strong></h3><ul><li>Variable wavelength UV/VIS detector <strong>for analytical HPLC and FPLC</strong></li><li>Simultaneous monitoring of <strong>up to 4 UV/VIS wavelengths</strong></li><li>Broad wavelength range from <strong>190 to 900 nm</strong></li><li>Optional conductivity monitoring up to <strong>1000 mS/cm</strong></li><li>Integrated temperature monitoring</li><li>Optional real-time pH measurement</li><li>Compatible with patented KNAUER CombiLight flow cell technology</li><li>Convertible between flow-cell and fiber-optic configurations</li><li>Internal holmium oxide filter for wavelength verification</li><li>Adjustable leak sensor for enhanced operational safety</li><li>Front-access lamp and flow-cell replacement</li><li>Comprehensive GLP functionality with component recognition</li><li>Suitable for analytical, preparative, and purification workflows</li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels:</strong><ul><li>4 × UV/VIS</li><li>1 × Conductivity</li><li>1 × Temperature</li><li>1 × pH</li></ul></li><li><strong>Wavelength range:</strong> 190–900 nm</li><li><strong>Light source:</strong><ul><li>High-brightness deuterium lamp</li><li>Halogen lamp</li><li>Integrated GLP chip</li></ul></li><li><strong>Flow cell:</strong> Not included</li><li><strong>Optional display:</strong> Mobile Control</li></ul><h4><strong>UV/VIS Performance</strong></h4><ul><li><strong>Spectral bandwidth:</strong> 6 nm (FWHM)</li><li><strong>Wavelength accuracy: </strong>±1.5 nm</li><li><strong>Wavelength precision:</strong> 0.4 nm</li><li><strong>Baseline noise: </strong>±7.5 µAU at 254 nm</li><li><strong>Baseline drift:</strong> 200 µAU/h at 254 nm</li><li><strong>Linearity: </strong>&gt;2.5 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>100 Hz (single UV channel)</li><li>5 Hz (four UV channels)</li></ul></li></ul><h4><strong>Conductivity Monitoring</strong></h4><ul><li><strong>Measurement range: </strong>0.1–1000 mS/cm</li><li><strong>Accuracy:</strong> ±2% or ±0.5 mS/cm (whichever is greater)</li></ul><h4><strong>pH Monitoring</strong></h4><ul><li><strong>Measurement range: </strong>pH 0–14</li><li><strong>Accuracy: </strong>±0.1 pH (between pH 2–12)</li></ul><h4><strong>Temperature Monitoring</strong></h4><ul><li><strong>Measurement range</strong>: 1–99 °C</li><li><strong>Accuracy</strong>: ±1.5 °C (4–40 °C)</li></ul><h4><strong>System Functions</strong></h4><ul><li>Internal holmium oxide filter for wavelength verification</li><li>Adjustable leak sensor</li><li>Automatic integration time</li><li>User-selectable time constants:</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp recognition</li><li>Operating hours tracking</li><li>Light source lifetime monitoring</li><li>Flow-cell recognition</li><li>Detailed GLP reporting</li></ul><h4><strong>Maintenance</strong></h4><ul><li>Front-accessible deuterium lamp</li><li>Front-accessible halogen lamp</li><li>Front-accessible flow cell</li><li>Simplified service procedures</li></ul><h3><strong>Applications</strong></h3><ul><li>Analytical HPLC</li><li>FPLC systems</li><li>Protein purification</li><li>Biopharmaceutical analysis</li><li>Process chromatography</li><li>Preparative chromatography</li><li>Method development</li><li>Quality control laboratories</li><li>UV/VIS monitoring of purification processes</li></ul>

KNAUER AZURA UVD 2.1L UV/VIS Detector

Compact and affordable UV/VIS detector for routine HPLC and fast LC applications, featuring 190–750 nm wavelength range and flexible flow-cell options.

<p><strong>The KNAUER AZURA® UVD 2.1L is a cost-effective UV/VIS detector designed for routine HPLC applications, including fast liquid chromatography methods. Combining reliable performance, compact dimensions, and flexible flow-cell options, it provides an ideal solution for analytical and preparative chromatography laboratories seeking dependable UV detection at an attractive price point.</strong></p><p>The detector utilizes a deuterium lamp covering the wavelength range <strong>from 190 to 750 nm</strong> and offers excellent sensitivity and stability for everyday chromatographic analysis. Its smart mechanical design allows quick and easy access to the flow cell, minimizing maintenance time and maximizing instrument uptime.</p><p>A wide range of interchangeable flow cells is available, including stainless-steel and bio-inert versions suitable for analytical, semi-preparative, and preparative LC applications with <strong>flow rates ranging from 10 μL/min up to 10 L/min</strong>. The detector integrates seamlessly into virtually any LC system through LAN communication, analog I/O, and compatibility with leading chromatography software packages.</p><h3><strong>Key Features</strong></h3><ul><li><strong>Cost-effective UV/VIS detector </strong>for routine HPLC applications</li><li>Suitable for fast LC methods</li><li>Wavelength range <strong>from 190 to 750 nm</strong></li><li>Single-channel variable wavelength detection</li><li><strong>Deuterium lamp </strong>with integrated GLP chip</li><li>Compact and robust instrument design</li><li>Easily accessible flow cell for rapid replacement</li><li>Wide selection of interchangeable flow cells</li><li>Compatible with analytical and preparative LC applications</li><li><strong>Flow rates from 10 μL/min up to 10 L/min</strong></li><li>Integrated leak sensor</li><li>Automatic integration time adjustment</li><li>LAN and analog communication interfaces</li><li>Comprehensive GLP functionality</li><li><strong>Compatible with ClarityChrom®, OpenLAB®, Chromeleon™, ChromGate®, PurityChrom®</strong>, and <strong>Mobile Control</strong></li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels:</strong> 1</li><li><strong>Light source: </strong>Deuterium (D₂) lamp with integrated GLP chip</li><li><strong>Wavelength range:</strong> 190–750 nm</li><li><strong>Spectral bandwidth: </strong>11 nm (FWHM)</li><li><strong>Wavelength accuracy:</strong> ±2.5 nm</li><li><strong>Wavelength precision:</strong> 0.3 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±15 µAU at 254 nm</li><li><strong>Drift: </strong>300 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>50 Hz via LAN</li><li>20 Hz via analog output</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Stainless-steel and bio-inert options available</li><li>Suitable for analytical and preparative chromatography</li><li>Flow rates from 10 μL/min to 10 L/min</li></ul><h4><strong>Communication and Control</strong></h4><ul><li>LAN communication</li><li>Analog input/output</li><li>Mobile Control software</li><li>Event control</li><li>Terminal protocol</li></ul><h4><strong>Inputs</strong></h4><ul><li>Error (IN)</li><li>Start (IN)</li><li>Autozero</li><li>0–10 V Analog (IN)</li></ul><h4><strong>Outputs</strong></h4><ul><li>Events 1–3</li><li>+5 V</li><li>24 V Valve</li></ul><h4><strong>Analog Output</strong></h4><ul><li>1 × 0–5 V scalable</li><li>20-bit resolution</li><li>Adjustable offset</li></ul><h4><strong>Programming Functions</strong></h4><ul><li>Timed wavelength programming</li><li>Event programming</li><li>Fraction valve control</li><li>Wake-up functions</li><li>Up to 9 programs</li><li>Up to 50 program lines</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp recognition</li><li>Operating hours tracking</li><li>Lamp operating hours</li><li>Lamp ignition counter</li><li>Detailed GLP reports</li></ul><h4><strong>Safety and Maintenance</strong></h4><ul><li>Integrated leak sensor</li><li>Easy-access flow cell compartment</li><li>Front-access maintenance</li><li>Minimal downtime for service operations</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><strong>Operating temperature:</strong> 4–40 °C</li><li><strong>Humidity:</strong> &lt;90% non-condensing</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply: </strong>100–240 V, 50–60 Hz</li><li><strong>Power consumption: </strong>65 W</li><li><strong>Dimensions (W × H × D):</strong> 361 × 158 × 523 mm</li><li><strong>Weight: </strong>5.9 kg</li></ul><h3><strong>Applications</strong></h3><ul><li>Routine HPLC analysis</li><li>Fast LC methods</li><li>Pharmaceutical quality control</li><li>Food and beverage analysis</li><li>Environmental testing</li><li>Chemical analysis</li><li>Preparative liquid chromatography</li><li>Academic and research laboratories</li></ul>

KNAUER AZURA UVD 2.1S UV Detector

Compact single-wavelength UV detector for routine HPLC applications with 190–500 nm range, flexible flow-cell options, and seamless software integration.

<p><strong>The KNAUER AZURA® UVD 2.1S is a compact, cost-effective single-wavelength UV detector designed for routine HPLC applications. Despite its small footprint, it delivers reliable performance and excellent technical specifications, making it one of the most compact HPLC UV detectors available on the market.</strong></p><p>Equipped with a deuterium lamp covering the <strong>wavelength range from 190 to 500 nm</strong>, the detector is suitable for a broad range of analytical chromatography applications. Its intelligent design provides quick access to the flow cell, enabling fast replacement and simplified maintenance. A wide selection of interchangeable flow cells is available, including bio-inert and stainless-steel versions for analytical and preparative LC applications with <strong>flow rates ranging from 10 μL/min up to 10 L/min</strong>.</p><h3><strong>Key Features</strong></h3><ul><li>Compact single-wavelength UV detector for HPLC</li><li>One of the smallest HPLC UV detectors available</li><li>Wavelength range <strong>from 190 to 500 nm</strong></li><li>Deuterium lamp with integrated GLP chip</li><li>Suitable for routine analytical applications</li><li>Compact AZURA® housing design</li><li>Easily accessible flow cell for rapid replacement</li><li>Wide range of interchangeable flow cells available</li><li>Compatible with analytical and preparative LC applications</li><li><strong>Flow rates from 10 μL/min up to 10 L/min</strong></li><li>Stand-alone operation via front panel</li><li><strong>LAN, RS-232</strong>, and analog communication interfaces</li><li>Compatible with major chromatography data systems</li><li>Available as a module for <strong>AZURA® ASM 2.2L</strong></li><li>Low maintenance requirements</li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels: </strong>1</li><li><strong>Light source:</strong> Deuterium (D₂) lamp with integrated GLP chip</li><li><strong>Wavelength range:</strong> 190–500 nm</li><li><strong>Spectral bandwidth: </strong>13 nm (FWHM)</li><li><strong>Wavelength accuracy: </strong>±3 nm</li><li><strong>Wavelength precision: </strong>0.7 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±20 µAU at 254 nm</li><li><strong>Drift:</strong> 300 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>50 Hz via LAN</li><li>20 Hz via analog output</li><li>10 Hz via RS-232</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Bio-inert and stainless-steel options available</li><li>Suitable for analytical and preparative chromatography</li><li>Flow rates from 10 μL/min to 10 L/min</li></ul><h4><strong>Communication and Control</strong></h4><ul><li>Front panel operation</li><li>Mobile Control software</li><li>Software control</li><li>Event control</li><li>Analog control</li><li>Terminal protocol</li></ul><h4><strong>Interfaces</strong></h4><ul><li>LAN (RJ-45)</li><li>RS-232 (SUB-D 9)</li><li>Multi-pin connector</li><li>Analog interface (RCA connector)</li></ul><h4><strong>Inputs</strong></h4><ul><li>Autozero</li><li>Start (IN)</li><li>Error (IN/OUT)</li><li>0–10 V Analog Input</li></ul><h4><strong>Outputs</strong></h4><ul><li>Error (OUT/IN)</li></ul><h4><strong>Analog Signals</strong></h4><ul><li>Analog wavelength input: 0–10 V</li><li>Analog output: 1 × ±2.5 V scalable</li><li>Resolution: 20-bit</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp operating hours monitoring</li></ul><h4><strong>Display</strong></h4><ul><li>LED display</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><strong>Operating temperature:</strong> 4–40 °C</li><li><strong>Humidity</strong>: &lt;90% non-condensing</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply:</strong><ul><li>Input: 100–240 V</li><li>Output: 24 V DC</li></ul></li><li><strong>Power consumption: </strong>60 W</li><li><strong>Dimensions (W × H × D):</strong> 121 × 129 × 187 mm</li><li><strong>Weight: </strong>1.5 kg</li></ul><h3><strong>Applications</strong></h3><ul><li>Routine HPLC analysis</li><li>Quality control laboratories</li><li>Pharmaceutical analysis</li><li>Food and beverage testing</li><li>Environmental analysis</li><li>Academic research</li><li>Preparative liquid chromatography</li><li>Compact and space-limited laboratory environments</li></ul>

Products from category UV-Vis HPLC detectors from KNAUER - page 1

Related content

ISC 2026 - Day 3

Droplet Cyclic Ion Mobility Mass Spec: Compressing Months of Enzyme Screening Into Just 14 Hours

ISC 2026 - Day 2