Quantifiable consistency. By tracking retention time consistency and peak symmetry across years of production, column performance becomes directly comparable.In chromatography, inconsistent separations are inconvenient and costly.Every unexpected shift in retention time or change in peak shape can trigger a cascade of troubleshooting, reruns, and uncertainty that slows laboratory productivity.On the other hand, when columns perform consistently, laboratories recover valuable time, reduce uncertainty, and maintain confidence in their data. True batch-to-batch consistency means fewer failed validations, fewer investigations, easier audits, and smoother collaboration across global sites.In regulated industries, data integrity underpins every decision, from early development to final release testing, so consistent column performance is a necessity.<h3>Key takeaways</h3><ul><li>Batch-to-batch (U)HPLC column consistency directly influences long-term method performance by stabilizing retention times, preserving peak shape, and supporting reliable validation of pharmaceutical methods.</li><li>Multi-year performance data across thousands of columns shows us how controlled column manufacturing reduces chromatographic variability, supporting reproducible results across column formats, batches, and laboratories.</li><li>Stable (U)HPLC columns minimize revalidation, troubleshooting, and method transfer challenges in regulated workflows, improving analytical efficiency across the product lifecycle.</li></ul><h3>Defining and measuring batch-to-batch (U)HPLC column consistency</h3>A (U)HPLC column is packed with <a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/chromatography/chromatography-learning-center/chromatography-consumables/consumable-types.html">solid-phase particles</a> that <a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/chromatography/chromatography-learning-center/liquid-chromatography-information/hplc-system-components/how-hplc-columns-work.html">separate compounds by chemical structure</a>.If medium composition differs even slightly between manufacturing batches, retention times and peak shapes can change. These differences might seem minor, but in pharmaceutical analysis they can trigger failed validations, unnecessary troubleshooting, and inconsistent data across labs.A recent evaluation of<a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/TG_20762_LC_Hypersil_GOLD_TG_20762_EN_ebcf64d4d6/TG-20762-LC-Hypersil-GOLD-TG20762-EN.pdf"> Thermo Scientific Hypersil GOLD columns</a> examined whether<a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/products?category=48&amp;manufacturerItems=3&amp;search=gold"> these columns </a>perform consistently across years of production. The answer: our results found sustained performance over time.Across roughly 17,500 columns tested over three years, researchers focused on two major indicators of a manufacturer’s column performance:<ul><li>Relative retention time (RRT), which is essentially how consistently compounds elute off the column.</li><li>Peak asymmetry, a reflection of column packing quality and how well peaks “behave.”</li></ul>In a recent technical note: <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/tn_004127_ccs_hypersil_gold_reversed_phrase_reproducibility_tn004127_na_en_d6375a67fb.pdf">Evaluation of batch-to-batch consistency of reversed-phase HPLC columns for long-term method validation</a>, we evaluated three column configurations: a 250 mm × 4.6 mm, 5 μm column; a 150 mm × 4.6 mm, 5 μm column; and 50 mm × 2.1 mm, 5 μm column, using a test mixture of five compounds selected to represent different hydrophobicities.Despite differences in column geometry and media batches, the method produced highly consistent chromatographic performance.The method also achieved RRT relative standard deviation variation of no more than 2.11% for the compounds and kept peak asymmetry within a narrow range of 0.92 to 1.09. This level of control reduces uncertainty from long-term method validation, reinforcing confidence in predictable, reproducible column performance.<h3>Why column stability over time matters</h3>As an experienced analyst, you already know how frustrating <a target="_blank" rel="noopener noreferrer" href="https://www.thermofisher.com/content/lifetech/global/en/home/industrial/chromatography/chromatography-learning-center/liquid-chromatography-information/hplc-method-development-steps.html">method validation</a> can be. You think you’ve nailed the method, only to find the results from run to run. Often, the issue isn’t you. It’s the tools.When your column behaves the same every time, you will see several downstream benefits, such as:1. Improved confidence in data interpretationYou don’t have to keep wondering whether differences in your data are coming from your chemistry or your column.2. Methods stay valid longerPharmaceutical companies must monitor drug purity throughout the product lifecycle, from development to manufacturing to quality control. A column that performs consistently over time makes comparisons straightforward and reliable.3. Method transfer is more reliableLarge companies operate across multiple global sites. When everyone uses columns that behave consistently, transferring methods becomes seamless rather than a months-long headache.A closer look at column performance dataThe published technical note visualizes column performance using clean, simple charts (Figure 1).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_What_Multi_Year_Batch_Data_Reveals_About_U_HPLC_Column_Consistency_18faa4e44c.jpg" alt="Thermo Fisher Scientific: What Multi-Year Batch Data Reveals About (U)HPLC Column Consistency: Figure 1.&nbsp; (Top image) Batch-wise average RRT, normalized by o-Xylene for Hypersil GOLDTM 250 mm x 4.6 mm 5 µm (83 batches). (Bottom image) Average peak asymmetry evaluation of o-xylene Hypersil GOLDTM 250 mm x 4.6 mm 5 µm (83 batches)." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_What_Multi_Year_Batch_Data_Reveals_About_U_HPLC_Column_Consistency_18faa4e44c.jpg 245w," sizes="100vw" width="1000" height="600">These graphs show us:<ul><li>Tight clusters of RRT points across 83 batches, depending on column format.</li><li>Nearly identical behavior between columns of different dimensions, which is a sign of effective manufacturing process controls.</li><li>Peak asymmetry values hovering around 1.0, indicating well-packed columns producing sharp, reliable peaks.</li></ul>This data might not seem glamorous at first glance, but for anyone who’s spent hours troubleshooting peak tailing, drifting retention times, or inconsistent quality control (QC) results, these charts are beautiful.<h3>Why column consistency matters for long-term method performance</h3>In automated LC workflows, a small change in column behavior can affect multiple downstream outputs: integration, peak purity assessment, and calculated assay/impurity results. Over time, this can translate into system suitability failures, drift outside validated ranges, and additional validation or comparability work.Column stability and batch-to-batch reproducibility are therefore critical for sustaining validated methods over time. The multi-batch data presented here demonstrate how controlled manufacturing processes can maintain consistent retention behavior and peak shape over time.To learn how to test your column and determine what data to look for, read our technical note, <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/tn_004127_ccs_hypersil_gold_reversed_phrase_reproducibility_tn004127_na_en_d6375a67fb.pdf">Evaluation of batch-to-batch consistency of reversed phase HPLC columns for long-term method validation</a>.<h3>FAQs</h3><div><div><h5>1. How does batch-to-batch consistency in LC columns affect chromatographic results?</h5>Batch-to-batch consistency has a direct impact on the stability of chromatographic results. When columns are manufactured consistently, retention times remain stable and compounds elute at predictable intervals — run after run and batch after batch. This stability reduces unexpected shifts in selectivity or peak shape, helping analysts distinguish true method-related changes from column-related variability.</div><div><h5>2. How do you measure batch-to-batch consistency in LC columns?</h5>Batch-to-batch consistency is evaluated by applying the same standardized test method to columns produced across multiple manufacturing lots and by comparing key chromatographic performance metrics. Commonly monitored parameters include RRT, which reflects retention stability and peak asymmetry, which indicates packing quality and peak integrity. By tracking these metrics over many batches and extended production periods, manufacturers can quantify variability and ensure controlled, reproducible column performance.</div><div><h5>3. How does batch-to-batch LC column consistency support long-term method validation and transfer between laboratories?</h5>Consistent LC column performance plays an important role in sustaining validated methods over time, particularly in regulated pharmaceutical environments. When column behavior remains stable across production batches, methods are more likely to stay within established acceptance criteria, reducing the need for revalidation or investigation. This stability is especially valuable throughout the product lifecycle, from development through quality control and release testing. Batch-to-batch consistency also facilitates smoother method transfer between laboratories and global sites. When different labs use columns that perform the same way, chromatographic results are more predictable, making transfers faster, more efficient, and less prone to variability-related delays.</div></div><blockquote>Visit us on&nbsp;<a target="_blank" rel="noopener noreferrer" href="https://www.linkedin.com/showcase/72003132/admin/dashboard/">LinkedIn:</a>&nbsp;#UHPLC #ColumnsAndConsumables #pharmaceutical</blockquote>

What Multi-Year Batch Data Reveals About (U)HPLC Column Consistency

Chromatogram-based library searching can provide a fast first identification, but it does not always give analysts the flexibility needed to evaluate alternative candidates, adjust precursor settings, or choose different spectral comparison strategies. In his presentation, James Little of Mass Spec Interpretation Services shows how <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/Chromatogram_Sent_to_Lib_Search_d324bc4118.pdf">transferring chromatogram results into the standard NIST Library Search window</a> can expand the available search options and provide a more detailed view of potential compound matches.The workflow is particularly relevant when an analyst wants to go beyond the single best chromatogram result and investigate alternative library candidates, compare spectra using different scoring approaches, or perform MS/MS searches with greater control over precursor information.<h3>Why move from the chromatogram to Library Search?</h3>The chromatogram view is useful for rapid inspection, but according to the presentation, its library-search functionality is more limited.One of the main differences is that the chromatogram result list displays only the best library result, while the standard Library Search window provides access to alternative candidates. This can be important when several structures produce similar spectra or when the highest-ranked match needs additional scrutiny.The standard Library Search window also provides more control over MS/MS searching. While searches initiated directly from the chromatogram use the precursor information automatically supplied by the chromatogram, the Library Search window allows the user to work with different search modes and modify precursor settings where required.To transfer a component from the chromatogram into Library Search, the workflow shown in the presentation is straightforward: right-click the component of interest and select “Library Search.”<h3>Identity and similarity searches</h3>Once the spectrum has been transferred, the search settings determine how the library comparison is performed.With Identity selected, an MS/MS search can reproduce the type of search performed from the chromatogram. If the “In spectrum” option is enabled, the precursor sent from the chromatogram is used automatically. The option can also be disabled, allowing the analyst to enter a different precursor manually.An additional option is HiRes No Precursor. In this mode, the spectra are compared without restricting the search according to the precursor ion. The presentation highlights this approach as useful for obtaining substructural information, since the comparison is not constrained to entries matching a specified precursor.The Similarity mode provides access to Hybrid Search. Here again, the precursor imported from the chromatogram can be used automatically or replaced by another value. Hybrid Similarity itself is treated separately in the source presentation series, but its availability is one of the reasons for working in the full Library Search environment.<h3>Choosing the right spectral matching method</h3>The Library Search window also provides several ways to score spectral similarity:<ul><li>Full Spectrum Search</li><li>Impurity Tolerant Search (Reverse-Dot)</li><li>Partial Spectrum Search (PSS-Dot)</li></ul>Each is designed for a different analytical situation.<ul><li>Full spectrum matching compares the complete experimental and library spectra and is most appropriate when the acquired spectrum is clean and complete.</li><li>Reverse-Dot matching focuses primarily on whether important peaks from the library spectrum are present in the experimental spectrum. Extra peaks in the measured spectrum that are absent from the library spectrum are not penalized in the same way. This can make the approach more tolerant of chemical background or spectral contamination.</li><li>Partial Spectrum Search addresses the opposite situation. It does not strongly penalize library peaks that are missing from the experimental spectrum and is therefore suited to incomplete spectra, including cases where only a subset of fragment ions is observed, such as some MS/MS or filtered datasets.</li></ul>Although the results table can display multiple similarity metrics, the search method selected before the search begins is important because of the way Presearch operates.<h3>Why Presearch matters</h3>NIST uses a Presearch step to reduce the number of library spectra that require more detailed comparison.This significantly increases search speed, but it also means that spectra removed during Presearch will not appear later in the final results—even if another scoring metric might have ranked them favorably.This is why the presentation emphasizes choosing the appropriate search method before Presearch when Reverse-Dot or Partial Spectrum behavior is important.For example, running a standard Full Spectrum search and then sorting the final result table by Reverse-Dot does not necessarily reproduce the same candidate set that would have been obtained if an impurity-tolerant search had been selected from the beginning. Potentially relevant candidates may already have been excluded during the initial Presearch stage.For routine reviewing, the presentation recommends using the overall NIST Score as the primary sorting criterion, while remembering that specialized searches may require a different search strategy from the outset.<h3>Selecting libraries and mass tolerances</h3>Before running the search, analysts can specify which libraries should be included.The presentation illustrates the Library Search settings where individual spectral libraries can be added or removed from the search. This allows the search space to be tailored to the application rather than automatically searching every available library.For high-resolution MS/MS data, users can also configure mass tolerances for both precursor and product ions.These settings are particularly important because overly broad tolerances may increase the number of irrelevant candidates, while unnecessarily narrow tolerances could exclude valid matches. The appropriate values therefore need to reflect the quality and mass accuracy of the acquired data.The software also provides additional options associated with precursor handling and polarity matching.<h3>Understanding the result scores</h3>Once the search is complete, the result table can be customized to support efficient review.Properties can be added, reordered, resized, and used for sorting. The presentation notes that the results are normally best reviewed initially by Score.Two related measures discussed are the dot product and the NIST Score.The dot product reflects the direct similarity between two spectra based on shared peaks and their intensities. The NIST Score builds on this comparison by applying additional weighting and scaling. According to the presentation, this helps preserve useful matching performance when spectra are incomplete, as may occur with MS/MS or filtered spectral data.Analysts can also sort by Rev-Dot or Partial Spectrum Search (PSS) values. However, the limitations imposed by the initial Presearch still apply: sorting cannot recover candidates that were already removed before the detailed comparison stage.The result interface can also be navigated efficiently using the keyboard arrow keys, and the available display properties can be rearranged according to the analyst’s preferred review workflow.<h3>Additional filters for faster review</h3>The presentation also highlights two useful post-search filters:<ul><li>Best Matching Only</li><li>MS/MS Hit Filter List options</li></ul>Unlike Presearch, these filters are applied after the candidate search has already been completed. They can therefore be switched on and off without permanently removing candidates from the search process.The Best Matching Only option removes many duplicate results and can make the candidate list easier to review.The MS/MS Hit Filter provides additional filtering options for tandem MS results, including parameters related to instrument type and allowed precursor forms.James Little notes that he generally keeps these filters disabled initially and applies them only when needed. This approach preserves the complete search result set during the first review and allows filtering to be introduced later as a tool for improving efficiency.<h3>More flexibility for library-based identification</h3>The main advantage of moving chromatogram results into the full NIST Library Search window is not that the original chromatogram search is incorrect, but that the dedicated search environment gives the analyst more control over how the spectrum is interrogated.It allows alternative candidates to be reviewed, precursor restrictions to be modified, different identity and similarity strategies to be selected, and specialized full-spectrum, impurity-tolerant, or partial-spectrum comparisons to be performed.Just as importantly, the workflow highlights a subtle but important principle in spectral searching: the scoring method used to review results and the method used to generate the candidate set are not necessarily interchangeable. Because Presearch determines which library spectra proceed to detailed evaluation, analysts should choose the search strategy that best reflects the characteristics of their experimental spectrum before beginning the search.Used in this way, the NIST Library Search window can provide a more flexible and transparent workflow for investigating chromatographic components and evaluating MS/MS library matches.

 Searching Normal NIST Search with Chromatogram Results

Is your lab ready for the new academic year? As students and teachers return to the laboratory, now is a great time to prepare your chromatography systems for the semester ahead.Now with 20% total discount on a new <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/999">Clarity Chromatography Software</a> for customers from educational institutions. In addition, customers purchasing a new license for Clarity Chromatography Software will receive a free copy of <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/1000">Clarity Offline Chromatography Software</a>.<blockquote>👉Promotion code: MKT2114The offer is valid through the end of October 2026.</blockquote>The latest version of Clarity Chromatography Software - 10.2 was released in June 2026! <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/article/7512">Read the article HERE.</a>

Back to School: 20% Off Clarity Chromatography Software

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Since 1991 DataApex develops and manufactures chromatography data stations. DataApex is constantly striving to provide users with efficient and up-to-date tools for chromatography data processing.

DataApex

A unique company dedicated to serving science helping our customers drive productivity and accelerate results. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services.

Thermo Fisher Scientific

My main interest is the identification of organic compounds by mass spectrometry in organic mixtures.

James Little/Mass Spec Interpretation Services

Wasson GC O-FID Oxygenated Components in Gasoline Analyzer

Using an Agilent Technologies 8890 with custom Wasson-ECE hardware, this instrument rapidly determines oxygenate components in motor fuels.

Approved for determining oxygenates in gasoline and other motor fuels by ASTM D5599 and EN 1601
The determination of oxygenates in motor fuels is an important mandate of the reformulated fuels program. To meet this goal, the United States Environmental Protection Agency approved the use of Oxygenate Flame Ionization Detector (O-FID) analysis in preference to other analyses currently used by the fuels industry.
<h5>Oxygen Selectivity</h5>
Using an Agilent Technologies 8890 GC with custom Wasson-ECE hardware, this instrument rapidly determines oxygenate components in motor fuels. A single injection is introduced onto a capillary column which separates oxygenate components in boiling point order. A cracking reactor converts hydrocarbons into elemental carbon, and oxygenated compounds into carbon monoxide. A methanizer then further converts the carbon monoxide into methane before eluting to the FID detector.
Because hydrocarbons never make it to the detector, this method completely eliminates problems with hydrocarbon interferences.
<h5>Single GC 8890 Instrument Configurations:</h5>
<ul>
<li>ASTM D5599 or EN1601 - Oxygenates in gasoline and other motor fuels by O-FID.
</li>
<li>O-FID with D3606 - Oxygenates by O-FID per ASTM D5599 and benzene and toluene in motor fuels by FID per ASTM D3606
</li>
<li>O-FID with D4815 - Oxygenates by O-FID per ASTM D5599 and oxygenates by FID per ASTM D4815
</li>
<li>O-FID with D4815 and D3606 - Oxygenates by O-FID per ASTM D5599, oxygenates by FID per D4815, and benzene and toluene by FID per ASTM D3606
</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_O_FID_GC_analyzator_kyslikatych_latek_Ukazkovy_chromatogram_z_O_FI_Du_32e439263e.jpg" alt="Wasson: Example chromatogram from O-FID GC system"/>
<h5>Simple to Use and Operate</h5>
The Wasson-ECE O-FID has been engineered to provide long life and require infrequent service. When replacement of the cracking reactor or methanizer is necessary, the task can be accomplished in under one hour, including instrument equilibration time.
<h5>Precise Analyses</h5>
Repeatibility tests yield relative standard deviations (RSD) of approximately 1% by weight over a series of 10 runs for all major oxygenated components. The O-FID response is linear over four orders of magnitude. An automated injection device is recommended to provide the most reliable means of repeatable injection.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_O_FID_GC_analyzator_kyslikatych_latek_Opakovatelnost_mereni_51c93d3988.jpg" alt="Wasson: GC O-FID Oxygenated Components in Gasoline Analyzer - Repeatibility tests"/>

Wasson-ECE GC RGA Refinery Gas Analyzers

Wasson-ECE Refinery Gas Analyzers (RGA) are an integral part of any HPI lab. 

Wasson-ECE Refinery Gas Analyzers (RGA) are an integral part of any HPI lab. These instruments often carry the heaviest sample loads because of the critical information they provide. RGAs provide valuable information regarding plant operation, unit optimization, and quality control. Our RGA systems are designed for flexibility while maintaining the accurate and repeatable results our clients have come to expect.
As a premier channel partner of Agilent Technologies, Wasson-ECE extends the capabilities of the 8890 Gas Chromatograph to meet key requirements of refinery gas analysis. The Wasson-ECE RGA incorporates our specially designed auxiliary oven, which holds up to five additional rotary valves and six columns, extending the analysis capabilities far beyond traditional methods.
At Wasson-ECE we strive to produce a product that is innovative and state-of-the-art to help our customers overcome their analytical challenges. The flexibility of our RGA systems can ease bench space issues by combining analyses into a single instrument while maintaining an easy to service system with minimal downtime.
<h3>RGA Features</h3>
<ul>
<li>Complete range of analyzers for refinery and other petroleum gases and liquids
</li>
<li>vIncludes method development, selection of valves, and columns** in all configurations
</li>
<li>Dual TCDs and a single FID for the simultaneous analysis of fixed gases and hydrocarbons
</li>
<li>Wasson-ECE Auxiliary Oven which provides a second thermal zone
</li>
<li>Customized reports including calculations for mole %, weight %, or volume %, and calorific value available
</li>
<li>Optional liquid sampling valves or On-board Vaporizer expands the analytical capabilities to liquefied gases
</li>
<li>Optional fourth detector available on all Super RGA configurations
</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_RGA_GC_analyzator_rafinerskych_plynu_Wasson_ECE_Moznosti_konfigurace_RGA_17545e3d4c.jpg" alt="Wasson: Wasson-ECE RGA Configuration Options"/>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_RGA_GC_analyzator_rafinerskych_plynu_Ukazkovy_chromatogram_standardni_RGA_1b72a88528.jpg" alt="Wasson: 383-Standard Refinery Gas Analysis"/>
<h3>Wasson-ECE Super RGA</h3>
Wasson-ECE has the unique ability to add a fourth detector to the GC, building our Super RGA series of analyzers. The additional detector expands the analytical capabilities of the standard RGA to accommodate applications such as sulfurs, oxygenates, heavy hydrocarbons, and trace CO/CO₂. This increased flexibility in configurations can reduce the number of GC’s used in a lab, saving clients valuable bench space and time.
<h5>Performance Guarantee</h5>
From hardware to analysis we stand behind our quoted application. Prior to shipping the instrument, chromatograms are submitted for customer approval. Performance is guaranteed to the clients actual sample, not just a generic standard. Any problems with the application during the first year are covered under warranty for an unparalleled performance guarantee.
<h3>The Wasson-ECE Turn-key Process</h3>
<h5>Sales</h5>
<ul>
<li>Application designed to customer&#39;s requirements</li>
</ul>
<h5>Factory Application</h5>
<ul>
<li>Method development and application setup</li>
<li>Customer samples are run to verify performance</li>
<li>Chromatograms are sent for client approval</li>
<li>Factory acceptance training if desired</li>
</ul>
<h5>Installation</h5>
<ul>
<li>Experienced Wasson Field Service Technician</li>
<li>Analysis of client’s real world samples</li>
<li>Calibration and familiarization</li>
</ul>
<h5>Customer Satisfaction</h5>
<ul>
<li>Follow up after installation</li>
<li>Knowledgeable and responsive service team</li>
<li>Optional preventative maintenance visits or service contracts</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_RGA_GC_analyzator_rafinerskych_plynu_Ukazkove_chromatogramy_Super_RGA_c62a4d715e.jpg" alt="Wasson: Example chromatograms (Super RGA)"/>

Wasson GC DHA Hydrocarbon Expert software

DHA analysis easy and simple. Efficient analysis is now even more efficient. Hydrocarbon Expert software.

Wasson-ECE Dragon DHA is a fast, easy to use application for the detailed hydrocarbon analysis of petroleum products by high efficiency gas chromatography. Dragon DHA uses a convenient, graphical interface to provide a one-screen display for visually observing the chromatogram and manipulating the data calculations in order to obtain the optimum results for analysis and data presentation.
<h3>Dragon DHA Includes:</h3>
<ul>
<li>Quick database creation.
</li>
<li>Fast peak identification and results processing.
</li>
<li>“Unknown” tab lists unidentified peaks in order of concentration.
</li>
<li>“Unknown indexer” takes the user directly to the unknown peak for identification.
</li>
<li>Unique dashboard feature continuously presents the user with all calculated results and instantly recalculates when changes are made.
</li>
<li>Hydrocarbon group-type filtering.
</li>
<li>Full preview and printing of reports.
</li>
<li>Results are bound with chromatographic data for instant retrieval and archiving. 
</li>
<li>Original files and data are never affected (CFR Part 11/ISO 17025).
</li>
<li>Result files are saved as netCDF (.AIA) format files and can be accessed by any third-party application that supports reading .AIA file format.
</li>
<li>Result files work as fully functional reference databases.
</li>
<li>Full reports are stored with results for easy retrieval without reprocessing.
</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_Obrazek_1_Diagram_casti_DHA_chromatogramu_s_identifikovanymi_a_neidentifikovanymi_piky_b50386d9b9.jpg" alt="Wasson: Diagram of the part of the DHA chromatogram with identified and unidentified peaks. Hydrocarbon Expert greatly simplifies the identification of components by comparing the measured chromatogram with a reference."/>
<h3>Wasson-ECE Dragon DHA Software</h3>
Wasson-ECE Instrumentation Dragon DHA software uses integrated chromatographic data from commercial GC data systems, i.e. ChromPerfect, EZ Chrome, ChemStation. In fact, any GC data system capable of AIA (ANDI) file output is compatible with Dragon DHA.
<h3>Chemical and Physical Property Calculations</h3>
<ul>
<li>Vapor pressure</li>
<li>Oxygenate content</li>
<li>Relative density</li>
<li>Average molecular weight</li>
<li>Calculated research octane number</li>
<li>% carbon, % hydrogen</li>
<li>Calculated bromine number</li>
<li>Mass% and vol% multi-substituted ring aromatics</li>
<li>Total boiling point distribution</li>
<li>Wt%, vol%, mole% of group types by carbon number</li>
<li>Wt%, vol%, mole% of individual components</li>
</ul>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Altium_International_Wasson_Obrazek_5_V_software_lze_porovnavat_neomezeny_pocet_signalu_a_reportu_Srovnani_lze_provest_na_jakekoli_urovni_od_shrnuti_dle_skupin_po_vlastni_vypocty_9c06f36d16.jpg" alt="Wasson: An unlimited number of signals and reports can be compared in the software. Comparisons can be made at any level, from group summaries to custom calculations."/>

Wasson Pressurized Liquid Auto-sampler (LS100B)

Wasson-ECE Liquid Auto-Sampler (LS100B) offers laboratory automation for pressurized liquid samples such as liquefied petroleum gas (LPG) and natural gas liquids (NGL).

Wasson-ECE Liquid Auto-Sampler (LS100B) offers laboratory automation for pressurized liquid samples such as liquefied petroleum gas (LPG) and natural gas liquids (NGL).
The LS100B uses inert gases to maintain pressure so that the sample remains in the liquid state at ambient temperature as it passes to the GC for analysis.
The LS100B accommodates up to nine sample cylinders with 1/4 inch tube, VCO, or quick connect fittings. These fittings hold the sample cylinders vertically, ensuring that samples are drawn from the bottom of the cylinder.
<h4>Pressurized Liquid Auto-sampler Features</h4>
<ul>
<li>Purges automatically with carrier gas between each sample run
</li>
<li>Remote-starts the GC and the data recording software such as ChemStation™
</li>
<li>Adds a date/time stamp to all samples
</li>
<li>Holds up to nine 3.5 inch / 8.9 cm diameter sample cylinders
</li>
<li>Works with standard open or floating-piston sample cylinders
</li>
<li>Pauses automatically when it detects that the GC is not running or not ready
</li>
<li>Can interrupt the scheduled sample sequence to process a priority sample
</li>
</ul>

Wasson Dynamic Blender for GC (DB302)

The Dynamic Blender is a portable gas blending device that dilutes a sample or a certified standard with a matrix gas of choice.

Gas chromatography (GC) analyses often include trace level detection of components requiring samples or standards at low concentrations. Some analytes are expensive or difficult to purchase at low levels due to reactivity, adsorption, or high molecular weight. Analyses may also cover a wide concentration range, requiring multi-point calibration.
The Wasson-ECE Dynamic Blender (DB302) provides a simple solution to these calibration needs. The Dynamic Blender is a portable gas blending device that dilutes a sample or a certified standard with a matrix gas of choice. One certified standard with concentrations at the upper limit of the desired calibration curve can be diluted to a lower level (&gt;2 orders of magnitude lower) to create a full calibration curve.
An inert flow path and heated bridge eliminate adsorption and condensation problems when blending gas standards that include sulfur, nitrogen, and other reactive compounds.
An on-board flow controller allows the diluent gas flow to be controlled digitally and samples are fed directly to a gas chromatograph. The Dynamic Blender eliminates the need to purchase and store multiple gas cylinders and provides an easy, cost-effective solution for gas phase calibration needs.
<h4>Dynamic Blender Features</h4>
<ul>
<li>Approximately 100 pre-programmed pure diluent gases and mixtures and twenty user configurable diluent mixture slots.
</li>
<li>Maximum Diluent Pressure of 100 psi (leak tested to this pressure)
</li>
<li>Maximum Temperature of 150°C (operation verified at this temp.)
</li>
<li>Mass Flow Controller Range of 10 – 500 cc/min
</li>
<li>7 μm in-line gas filters (treated) are also provided
</li>
<li>Specially passivated tubing for trace reactive compounds (sulfurs, oxygenates, etc.)
</li>
</ul>
*This treatment is not suitable for samples with pH &gt; 8.0, so please notify your sales representative if you have high pH samples.

Wasson Variable Pressure Sampler (VPS)

The Variable Pressure Sampler (VPS) works in two ways to ensure the precision and accuracy of gas results.

The Variable Pressure Sampler (VPS) works in two ways to ensure the precision and accuracy of gas results. The first method is pressure correction, used to create uniform pressure among all injected samples and the calibration blend. The second method is multi-point calibration, which can deliver a calibration blend to the GC at various pressures.
The VPS pressure correction system performs a multi-step process that ensures samples and calibration blends are at uniform pressures when they are injected.
First, when the calibration blend is run through the GC, the VPS measures and stores the pressure of the calibration blend at the time of injection. Then, as each sample is injected at the stored pressure, the VPS adjusts the pressure of the sample to match the pressure of the calibration blend.
The inject pressure of the sample is reported to Agilent Technologies OpenLAB ChemStation software so calculations and quality control operations can be performed.
Using the VPS, calibration samples can be run at various pressures from a single standard. This decreases overall lab costs while ensuring greater accuracy in results. The multi-point calibration function allows testing for signal linearity at different pressures. With this feature, the user can easily pinpoint the range of pressures which generates the most accurate and meaningful results from the calibration standard.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Wassson_Variable_Pressure_Sampler_VPS_linearity_77314725d6.jpg" alt="Wassson: Variable Pressure Sampler (VPS) - linearity"/>

Wasson LPG Vaporizer (1107)

The LPG Vaporizer uses an innovative, proprietary technique to vaporize liquid samples for injection in an existing GC system.

The LPG Vaporizer uses an innovative, proprietary technique to vaporize liquid samples for injection in an existing GC system. This convenient laboratory system offers flexibility and accuracy for both gas and liquid samples.
The LPG Vaporizer is more convenient than a typical liquid sample valve with more accurate results. All liquid samples are vaporized and run at a constant pressure, eliminating sample density changes that cause errors in liquid phase samples. This ensures sharp, easy-to-read peaks for all samples.
The LPG Vaporizer is built with specially passivated parts for analyzing trace reactive analytes such as sulfurs and oxygenates.
Wasson-ECE&#39;s unique, proprietary vaporization technique produces an even and accurate gas sample. Other vaporizers use tubing with a large volume, causing samples to fractionate when vaporized. This can lead to incomplete sample analysis. The LPG Vaporizer controls the injection volume so that all elements in the liquid sample are vaporized and sent to the GC simultaneously, producing a complete and accurate analysis of the sample.
<h4>LPG Vaporizer Features</h4>
<ul>
<li>Inject liquid and gas samples with a single valve
</li>
<li>High sample throughput
</li>
<li>Purging technique reduces cross-contamination
</li>
<li>Ability to stop sample flow to the GC at any time
</li>
<li>Controlled injection volume
</li>
<li>4 ft. heated bridge from vaporizer to customer&#39;s GC sample valve to prevent sample re-condensing
</li>
</ul>

Wasson Gas Auto-sampler (AS202)

The Gas Auto-sampler (AS202) is a stand-alone device that delivers samples to the GC through a heated bridge, ensuring that samples are injected at the appropriate temperature.

The Gas Auto-sampler (AS202) is a stand-alone device that delivers samples to the GC through a heated bridge, ensuring that samples are injected at the appropriate temperature. The heated pathway is purged with carrier gas between each sample injection, and a vacuum pump ensures an extremely low level of matrix cross-contamination (typically less than 50 ppm).
Samples are loaded into the AS202 oven, which can hold up to twelve 500cc sample cylinders or nine 1L cylinders. The shelves are removable and adjustable and can also be tilted to prevent injection of any residual liquids which then changes the setup to allow for a maximum of eight 500cc or six 1L cylinders.
Samples (1000 psig / 6895 kPa max) are automatically regulated during the purging sequence so the GC injects all samples and calibration blends at atmospheric pressure. The AS202 can also be configured to automate injection of samples that are already at atmospheric pressure.
The table below compares the GC analysis results for 2 mL samples of n-pentane and n-hexane at 100 psig in propane. In the first trial, the sample is sent to the GC from the AS202 at ambient temperature; in the second trial the AS202 heats the samples to 130°C before injection.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Wasson_Wasson_autosampler_pro_plynne_vzorky_Srovnani_vysledku_GC_analyz_f7c0ad0991.jpg" alt="Wasson: Repeatability Comparisons - Heated vs. Unheated"/>

Products focused on GC - page 1

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