<p><strong>Our Library never stops expanding. What are the most recent contributions to LabRulezGCMS Library in the week of 7th September 2026? Check out new documents from the field of the gas phase, especially GC and GC/MS techniques!</strong></p><blockquote><p><span style="font-size:20px;">👉 </span><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library"><span style="font-size:20px;"><strong>SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT GCMS AND RELATED TECHNIQUES</strong></span></a></p></blockquote><blockquote><p><strong>👉 Need info about different analytical techniques?</strong> Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library"><strong>LabRulezLCMS</strong></a> or <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library"><strong>LabRulezICPMS</strong></a> libraries.</p></blockquote><p>This week we bring you application notes by <strong>Agilent Technologies </strong>and <strong>Shimadzu, </strong>presentation by<strong> MDCW / Los Alamos National Laboratory </strong>and other document by<strong> Thermo Fisher Scientific!</strong></p><h3><strong>1. Agilent Technologies: Quantification of Microplastics in Soil and Sediment Using Dry-Ice-Assisted Fractionation</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_8700_ldir_chemical_imaging_system_5994_9256en_agilent_94102868f0.pdf"><strong>Full PDF for download</strong></a></li></ul><section><div><div><div><div><div><div><p>Microplastics are now widely reported in terrestrial environments, including soil and sediments, raising concerns about soil health and potential human exposure pathways (for example, in agricultural regions).1,2 Microplastics can be classified by polymer type and particle characteristics (size, color, and morphology such as fragments and fibers) and may be primary (manufactured small) or secondary (formed from the breakdown of larger plastic items). In this workflow, microplastics were defined as particles ranging from 1 µm to &lt;&nbsp;1,000 µm.&nbsp;</p><p>Reliable and reproducible quantification remains challenging, limiting comparability between studies and complicating risk assessment and the development of defensible monitoring approaches. Challenges occur across the workflow, from sampling and extraction through to instrumental analysis and reporting, and are exacerbated by environmental heterogeneity, inconsistent reporting, and the limited availability of standard reference materials and routine quality control&nbsp;procedures.&nbsp;</p><p>Conventional soil microplastics workflows typically include drying, density separation and/or flotation, chemical digestion to remove organic matter, and filtration prior to spectroscopic identification.3–5 In this application note, we combined a fast, practical extraction workflow with consistent, automated instrumental analysis by adapting foam fractionation to soil and sediment. Several bubbling strategies (soda water, compressed air, and nitrogen) were evaluated; dry ice was selected because it produced vigorous mixing and stable foam in the presence of a surfactant, enhancing exposure of particles to the foam layer and improving isolation from the matrix.&nbsp;</p><p>All method validation and environmental sample analyses were performed using an Agilent 8700 LDIR chemical imaging system, providing automated particle location, polymer identification, sizing, and counting. A particle-based internal standard was integrated into the workflow as a simple, sample‑specific check on extraction and transfer&nbsp;performance.</p><h4><strong>Results and discussion</strong></h4><h5><strong>Environmental sample overview&nbsp;</strong></h5><p>The workflow was applied to environmental samples from Victoria, Australia, including three soil types (chromosol, dermosol, and hydrosol) and freshwater sediment from three locations. In all samples, the <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/gcms/library?mainauthorItems=10&amp;search=8700%C2%A0LDIR"><strong>8700&nbsp;LDIR</strong></a> provided automated particle identification, sizing, and counting of microplastics following dry-ice-assisted fractionation and density separation. Soil concentrations ranged from 4,360 to 102,000 microplastics kg–1, with acrylonitrile butadiene styrene and polyamide the most frequently detected polymers. Sediment concentrations ranged from 41,400 to 127,000 microplastics kg–1 and were dominated by fragments in the 10 to 50 µm size&nbsp;range.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>This study demonstrates the suitability of the <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/gcms/library?mainauthorItems=10&amp;search=8700%C2%A0LDIR"><strong>Agilent 8700 LDIR chemical imaging system</strong></a> for automated, particle‑based quantification of microplastics in complex soil and sediment matrices. When combined with dry-ice-assisted foam fractionation, the 8700 LDIR provided reliable identification, sizing, and counting of microplastics across a broad size and density range with high&nbsp;repeatability.&nbsp;</p><p>The integration of a particle-based ISTD within the LDIR workflow enabled sample-specific performance assessment, addressing a key limitation in current microplastic methodologies. Application to environmental samples confirmed the robustness of the approach and highlighted the capability of the 8700 LDIR to support high‑confidence, reproducible microplastics analysis for research and routine monitoring applications.</p><h3><strong>2. MDCW / Los Alamos National Laboratory: Discovery-based analysis for chromatographic trends using alteration analysis (ALA) and two-dimensional correlation analysis (2DCOR)</strong></h3><ul><li>Presentation</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/O_1_Freye_10783a9cf3.pdf"><strong>Full PDF for download</strong></a></li></ul><section><div><div><div><div><div><div><p>The presentation focuses on discovery-based analysis of complex chromatographic datasets using <strong>Alteration Analysis (ALA)</strong> and <strong>Two-Dimensional Correlation Analysis (2DCOR)</strong>. The motivation is to avoid manual chromatogram comparison and labor-intensive peak-table processing, especially for GC-TOFMS and GC×GC datasets that can contain billions of data points. Instead, the authors analyze raw data directly and use statistical methods to identify only those features that show meaningful chemical changes across a series of samples.</p><p>ALA provides a quantitative way to detect how individual data points vary across a sample series. It generates three outputs: the <strong>Basic Alteration Map (BAM)</strong> for overall change, the <strong>Synchronous Alteration Map (SAM)</strong> for mainly linear changes, and the <strong>Asynchronous Alteration Map (AAM)</strong> for nonlinear behavior. Validation with simulated datasets showed that ALA can detect relatively small changes and remains effective even for severely overlapping chromatographic peaks. The presentation reports that its performance remains similar to that for isolated peaks down to a resolution of about <strong>Rs 0.3</strong>, and under suitable signal-to-noise and change conditions it can still succeed at resolutions as low as <strong>Rs 0.01</strong>.</p><p>While ALA identifies which signals are changing and the type or magnitude of that change, <strong>2DCOR adds information about how those changes are related to one another</strong>. Synchronous correlation maps describe whether signals change together in the same or opposite direction, while asynchronous maps help establish sequential relationships between changes. Using Noda’s rule, the order in which chemical features respond to an external perturbation can be inferred. The combined ALA–2DCOR workflow therefore provides three key pieces of information: <strong>the significance of a change, the relationship between changing components, and the order in which those changes occur</strong>.</p><p>Extending these methods to GC×GC required additional processing because of chromatographic misalignment and the enormous size of two-dimensional datasets, with GC×GC-HRMS data reaching roughly <strong>80 billion data points</strong>. The solution presented is to divide the chromatographic space into tiles, apply ALA to locate important features, then re-center tiles and use 2DCOR on the relevant regions. In a recent application to <strong>high-explosive aging</strong>, ALA detected more than <strong>250 chemical changes</strong>, providing insight into decomposition behavior where simpler feature-selection approaches such as the F-ratio were insufficient. The authors conclude that combining ALA and 2DCOR offers a practical route for discovering and interpreting chemical trends in highly complex GC-MS and GC×GC datasets.</p><h3><strong>3. Shimadzu: Residual Solvent Analysis in Pharmaceuticals with N2 Carrier Gas Using </strong><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/gcms/library?mainauthorItems=1&amp;search=GC-2060"><strong>Nexis GC-2060</strong></a><strong> and </strong><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/gcms/library?mainauthorItems=1&amp;search=HS-20+NX"><strong>HS-20 NX</strong></a></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_01_01172_en_59d0e341a0.pdf"><strong>Full PDF for download</strong></a></li></ul><h4><strong>User benefits</strong></h4><ul><li>The newly designed FID delivers outstanding sensitivity, ensuring highly accurate and reliable analysis.</li><li>Achieve full compliance with JP and USP guidelines using N2 carrier gas, which is highly affordable and readily available.</li><li>Easily analyzes tert-butyl alcohol and Cyclopentyl methyl ether, the Class 2 solvents added in the ICH Q3C (R8) guideline.</li></ul><p>For the analysis of residual solvents in pharmaceuticals, headspace gas chromatography (HS-GC) is widely used to target Class 1 and Class 2 solvents, in accordance with USP General Chapter &lt;467&gt; and JP18 (Japanese Pharmacopoeia, 18th Edition). These regulatory tests demand high sensitivity and reproducibility. The newly developed FID for the Nexis GC-2060 offers superior detection sensitivity compared to conventional models, enabling highly sensitive analysis. Additionally, due to recent helium supply shortages and rising costs, there is a growing demand for alternative analysis using nitrogen (N2) as a carrier gas.&nbsp;</p><p>This application note presents the analysis of Class 1 and Class 2 water-insoluble samples using the <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/gcms/library?mainauthorItems=1&amp;search=GC-2060"><strong>Nexis GC-2060</strong></a> with N2 carrier gas, compliant with Supplement II to the Japanese Pharmacopoeia. DMSO was used as the sample solvent.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>Using the Nexis GC-2060 with nitrogen (N2) carrier gas, we successfully achieved the analytical precision required by the Japanese Pharmacopoeia (JP18) and USP General Chapter &lt;467&gt;. The HS-GC method delivered excellent S/N ratios and high repeatability for the analysis of residual solvents in waterinsoluble pharmaceutical samples.</p><h3><strong>4. Thermo Fisher Scientific: Measuring and monitoring emissions at data centers: A practical guide to compliance and performance</strong></h3><ul><li>Other document (white paper)</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/datacenter_emissions_wp1802_en_45a9da8df3.pdf"><strong>Full PDF for download</strong></a></li></ul><p>The rapid expansion of data centers, driven by artificial intelligence (AI), cloud computing, and digital infrastructure, is creating unprecedented demand for electrical power. In many regions, utility interconnection delays, transmission constraints, and the need to bring new computing capacity online quickly are driving data center developers to incorporate onsite power generation as part of their energy strategy. Natural gas-fired turbines, reciprocating engines, and other distributed generation assets are increasingly being deployed to supplement or, in some cases, serve as the primary source of power for new facilities.&nbsp;</p><p>As data centers evolve from purely electrical loads into powergenerating facilities, they become subject to a range of air permitting, emissions reporting, and regulatory compliance requirements. Consequently, emissions monitoring has emerged as a critical component of both regulatory compliance and responsible facility operation. Facility owners and operators must balance the need for reliable power generation with increasingly stringent environmental requirements while maintaining operational performance and uptime.&nbsp;</p><p>This white paper provides a practical, technically grounded overview of emissions monitoring strategies for data centers with onsite power generation. It outlines the regulatory landscape, reviews common monitoring approaches, and discusses key system design considerations to help facility owners, operators, engineers, and environmental professionals develop effective compliance strategies while supporting the continued growth of digital infrastructure.</p><h4><strong>Analyzer technology considerations for modern CEMS&nbsp;</strong></h4><p>Gas analyzers form the core of any continuous emissions monitoring system. These instruments rely on well-established measurement principles that are recognized by regulatory agencies worldwide. Chemiluminescence detection (CLD), as described in EPA Method 7E², is widely used for NOx measurement due to its sensitivity, selectivity, and long-term stability. Similarly, non-dispersive infrared (NDIR) technology, as described in EPA Method 10³, is commonly used for carbon monoxide (CO) monitoring. These proven measurement techniques are broadly accepted across federal, state, and local regulatory programs and provide the accuracy and reliability required for emissions compliance applications. Selecting analyzer platforms that are widely deployed and familiar to regulators, testing organizations, and CEMS integrators can further simplify implementation, helping facilities achieve a smoother commissioning process and faster path to compliance.&nbsp;</p><p>Within this context, modern analyzer platforms like the <strong>Thermo Scientific™ 42iQ NO-NO2-NOx Gas Analyzer </strong>and the <strong>Thermo Scientific™ 48iQ CO Gas Analyzer</strong> have been specifically designed to support continuous emissions monitoring applications. These systems deliver high sensitivity, low detection limits, and stable performance across a wide range of operating conditions. Both analyzers can also be configured with optional oxygen (O₂) measurement capability, providing a convenient and cost-effective solution for monitoring NOx , CO, and O₂. This capability is particularly valuable in direct extractive CEMS configurations, where oxygen measurements are often required for emissions correction and reporting.&nbsp;</p><p>Seamless integration with data acquisition and handling systems (DAHS) is another key requirement for a modern CEMS. Analyzer platforms must support reliable data communication and interoperability, enabling consistent reporting and alignment with regulatory requirements.&nbsp;</p><p>Selecting the appropriate analyzer technology is a critical step in CEMS design. A well-designed analyzer solution not only supports compliance, it also contributes to long-term operational efficiency, reduced lifecycle costs, and confidence in emissions data.</p></div></div></div></div></div></div></section></div></div></div></div></div></div></section>

News from LabRulezGCMS Library - Week 37, 2026

News from LabRulezLCMS Library - Week 37, 2026

<p><strong>Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 7th September 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!</strong></p><blockquote><p><span style="font-size:20px;">👉 </span><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library"><span style="font-size:20px;"><strong>SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</strong></span></a></p></blockquote><blockquote><p><strong>👉 Need info about different analytical techniques?</strong> Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library"><strong>LabRulezLCMS</strong></a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library"><strong>LabRulezGCMS</strong></a> libraries.</p></blockquote><p>This week we bring you application notes by <strong>Agilent Technologies, Metrohm </strong>and<strong> Shimadzu </strong>and brochure by<strong> Thermo Fisher Scientific!</strong></p><h3><strong>1. Agilent Technologies: </strong><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=10&amp;search=9500"><strong>Agilent 9500 ICP‑QQQ</strong></a><strong> with m‑Lens for Ultratrace Analysis of High‑Purity Reagents</strong></h3><p><strong>Achieving low backgrounds under hot plasma conditions using ICP-QQQ preset methods&nbsp;</strong></p><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_m_lens_high_purity_reagents_9500_icp_qqq_5994_9062en_agilent_f0e65c4d9b.pdf"><strong>Full PDF for download</strong></a><strong>&nbsp;</strong></li></ul><p>Controlling trace-metal contaminants is essential in both semiconductor reagent analysis and metal‑based materials characterization. High‑purity chemicals such as nitric acid (HNO<sub>3</sub>) and sulfuric acid (H<sub>2</sub>SO<sub>4</sub>), as well as high‑purity metals, require analytical workflows capable of achieving sub‑ppt detection limits (DLs) while maintaining excellent robustness and reproducibility. To meet these needs, the <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=10&amp;search=9500"><strong>Agilent 9500 Triple Quadrupole ICP‑MS (ICP‑QQQ)</strong></a><strong> </strong>equipped with a Dual‑Cell System (DCS)<sup>1</sup> and the optional m‑lens ion optics provides a highly stable platform, enabling low backgrounds and reliable performance under hot plasma conditions.&nbsp;</p><p>The m‑lens is engineered to suppress background signals for elements including easily ionized elements such as Na and K that typically show elevated background equivalent concentrations (BECs) under hot plasma conditions. The 9500 ICP-QQQ with m‑lens is suitable for the analysis of metal digests and other sample types that demand robust performance and low backgrounds.<sup>2</sup></p><p>However, its benefits also extend to low‑matrix, high‑purity reagents, supporting sub‑ppt impurity measurements of simpler matrices.<sup>3&nbsp;</sup></p><p>Agilent’s ICP‑QQQ portfolio allows users to select instruments based on desired DLs and operational objectives. For laboratories seeking the lowest possible DLs, the Agilent 8900 Semiconductor configuration ICP-QQQ equipped with an s‑lens provides exceptional sensitivity, making it suitable for laboratories operating at the extreme limits of ultratrace quantification. The 9500 ICP-QQQ with m‑lens provides robust, high sensitivity measurements, ideal for routine trace level applications. This model is appropriate for labs that may not require the lowest DLs for every element but still demand high‑quality, reproducible data.&nbsp;</p><p>In this study, we evaluated the performance of the 9500 ICP‑QQQ using a method designed specifically for low‑matrix, high‑purity reagents. Using preset methods implemented in the instrument software for ultrapure water (UPW) and for H<sub>2</sub>SO<sub>4</sub> —the UPW method is also applicable to diluted HNO<sub>3</sub> and H<sub>2</sub>O<sub>2</sub> — we analyzed 1% HNO<sub>3</sub> and high purity H<sub>2</sub>SO<sub>4</sub> separately. Sub-ppt DLs and low backgrounds were achieved for target analytes in both matrices. These results confirm that the 9500 ICP‑QQQ with m-lens can be used for ultratrace impurity analysis of semiconductor‑grade reagents, as well as demanding metal‑matrix applications.&nbsp;</p><h4><strong>Experimental</strong></h4><h5><strong>Instrumentation&nbsp;</strong></h5><p>The <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=10&amp;search=9500"><strong>Agilent 9500 ICP-QQQ</strong></a> fitted with the optional m-lens and the Agilent I-AS autosampler were fully controlled using Agilent OpenLab ICP-MS software version 1.1. Designed for ultratrace metal analysis, the sample introduction system comprised a MicroFlow PFA nebulizer with I-AS probe (operated in self-aspiration mode), a temperature-controlled quartz spray chamber, and a quartz torch with a 2.5 mm inner diameter (id) injector. A platinum-tipped sampler cone with copper base and a platinum-tipped skimmer cone with nickel base for m-lens were used.&nbsp;</p><p>The 9500 ICP‑QQQ was operated using five tune modes: no gas, Advanced Helium Mode (AHM), O2 , NH3 , and H2 . For the H2 SO4 samples, additional specialized tunes were prepared for the determination of platinum (Pt) and zinc (Zn) to ensure optimal performance (Table 1). The use of reaction and collision gases enabled effective removal of spectral interferences originating from argon plasma species as well as matrix‑related polyatomic ions. The makeup gas flow rate and the Omega lens voltage parameters were automatically optimized by the preset methods for m-lens, resulting in a stable CeO/Ce ratio that was maintained between approximately 1 and 3%.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>This study evaluated the Agilent 9500 ICP‑QQQ with m‑lens for ultratrace analysis of high‑purity reagents using preset methods for 1% HNO3 and 9.8% H2 SO4 . Sub‑ or singlefigure ppt detection limits and low background equivalent concentrations were achieved for all elements, demonstrating that ultratrace measurements can be easily performed under hot‑plasma conditions. The Dual‑Cell System enabled effective removal of matrix‑related interferences, with Advanced Helium Mode providing an effective approach for the measurement of challenging elements such as Zn in H2 SO4 . The results show that the 9500 ICP‑QQQ with intuitive preset methods can deliver sensitive, low-background data, offering an accessible entry point for laboratories that are new to ultratrace analysis.</p><h3><strong>2. Metrohm: Rapid quality control of fruits and vegetables using NIR spectroscopy</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_nir_141_download_e1bab41aee.pdf"><strong>Full PDF for download</strong></a></li></ul><p>Near-infrared (NIR) spectroscopy has emerged as a powerful, nondestructive analytical technique for quality control in the fruit and vegetable processing industry. This Application Note presents the use of NIR spectroscopy for the rapid monitoring of firmness in apples and °Brix in peaches and crushed tomatoes. These are critical parameters to verify the quality and freshness of various fruits and vegetables. Traditionally measured using destructive methods like penetrometry and refractometry, these fresh produce quality control attributes are critical indicators of ripeness, sweetness, and overall consumer acceptability.</p><h4><strong>EXPERIMENTAL EQUIPMENT</strong></h4><p>All samples were tested with a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=220&amp;search=NIR"><strong>Metrohm near-infrared (NIR) spectrometer.</strong></a> The measurements were done in reflection mode using either a large sample cup or direct measurement (i.e., no holder). Metrohm software was used for all data acquisition and quantification model development.</p><h4><strong>CONCLUSION</strong></h4><p>This Application Note shows that NIR spectroscopy can easily measure firmness in apples, as well as °Brix in peaches and crushed tomatoes. When compared to traditional lab methods (Table 1), NIRS provides a faster, simpler, and nondestructive alternative with excellent accuracy and consistency. All measurements proved to be consistent and fast, helping producers to monitor their fresh fruits and vegetables and deliver high-quality products to consumers.</p><h3><strong>3. Shimadzu: Evaluation of Surface Carbon on Lithium-Ion Battery Cathode Active Materials Using a TOC Analyzer and Infrared/Raman Microscope</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_01_01122_en_b3b0f25211.pdf"><strong>Full PDF for download</strong></a></li></ul><h5><strong>User benefits</strong></h5><ul><li>The TOC solid sample measurement system enables quantitative evaluation of carbon coatings on cathode active material surfaces.</li><li>The AIRsight infrared/Raman microscope enables evaluation of the carbon layer structure.</li><li>Carbon content and structure can be evaluated using a small amount of sample.</li></ul><p>The cathode active materials used in lithium-ion batteries (LiBs) for electric vehicles (EVs) are broadly classified into two categories depending on their application: nickel-based materials (NCM/NCA/NCMA) and phosphate-based materials (LFP: LiFePO4, LMFP: LiFexMn1-xPO4). Nickel-based materials are characterized by high energy density as well as excellent low-temperature and high-power performance, making them indispensable for longrange driving and high-performance vehicle segments. In contrast, phosphate-based materials offer superior safety, long cycle life, and cost advantages, and their use is expanding primarily in standard-range and mass-market segments.</p><p>Because LFP and LMFP compounds are intrinsically low in electronic conductivity, a carbon coating on the surface of the active material is essential to compensate for that limitation and improve performance. Accordingly, quantitative control of carbon content is of great importance. For that type of carbon analysis, the TOC solid sample measurement system (Fig. 1), which combines a TOC-L total organic carbon analyzer with an SSM-5000A solid sample combustion unit, is effective.&nbsp;</p><p>Furthermore, the conductivity of the surface carbon layer is closely related to the degree of graphitization and defect structure of the carbon, making structural evaluation of the carbon layer equally important. The <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=1&amp;search=AIRsight"><strong>AIRsight infrared/Raman microscope</strong></a> (Fig. 2) enablessuch structural evaluation.&nbsp;</p><p>This Application News presents examples of evaluating carbon on the surface of LMFP cathode active materials, with carbon quantitation using a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=1&amp;search=TOC-L"><strong>TOC-L </strong></a><strong>+ </strong><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/icpms/library?mainauthorItems=1&amp;search=SSM-5000A"><strong>SSM-5000A system</strong></a> and carbon layer structure evaluation using the AIRsight infrared/Raman microscope.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>Quantitative analysis of the carbon coating on the LMFP surface was performed using the TOC solid sample measurement system (TOC-L + SSM-5000A), and structural evaluation of the carbon layer was conducted using the AIRsight microscope. In addition, Raman analysis of the LMFP residue after TC analysis was carried out to verify the validity of the carbon quantitation results. The TOC solid sample measurement system (TOC-L + SSM-5000A) is capable of not only TC analysis in solid samples, but also of IC and TOC analysis. Furthermore, by simply changing the software settings, carbon analysis of liquid samples (TOC, TC, and IC) can also be performed using the TOC-L main unit. This system can also be applied to carbon analysis of water-extractable TOC in black mass, lithium extraction solutions, and lithium carbonate, all of which are relevant materialsin lithium-ion battery recycling. The AIRsight is capable of both Raman and infrared measurements. Therefore, in addition to the Raman measurements introduced here, it can be used, with a single microscope system, to evaluate degradation caused by charge and discharge cycles in various battery components, such as negative electrode materials and separators.</p><h3><strong>4. Thermo Fisher Scientific: </strong><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/2002"><strong>Thermo Scientific GS Omni</strong></a><strong> Light Element Analysis in Slurry Process Streams</strong></h3><ul><li>Brochures and specifications</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/CAD_GS_Omni_Light_Element_Analyzer_bf50abdb7e.pdf"><strong>Full PDF for download</strong></a></li></ul><p>The <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/2002"><strong>Thermo Scientific™ GS Omni analyzer</strong></a> provides accurate, real-time elemental analysis of multiple slurry streams for both light and heavy elements. Using the Prompt Gamma Neutron Activation Analysis (PGNAA) technology, the GS Omni analyzer has a distinct advantage over analyzers using X-ray fluorescence (XRF) and Laser induced breakdown spectroscopy (LIBS) by being able to directly measure elements lower than calcium on the periodic table and particle sizes up to 5mm.</p><h4><strong>Benefits&nbsp;</strong></h4><p>The Thermo Scientific GS (Gamma Slurry) Omni analyzer is the latest development of a proven, robust, analyzer that provides direct simultaneous analysis of multiple elements in slurry beneficiation plants.&nbsp;</p><p>The analyzer is available in configurations of 2 to 8 streams. The optimum number of streams is usually dependent on the stream concentrations, elements of interest, required cycle analysis time, plant layout and process control considerations. This elemental analyzer will enable improvements in product quality, recovery and lower production costs.&nbsp;</p><h4><strong>Applications&nbsp;</strong></h4><p>The Thermo Scientific GS Omni analyzer is a powerful measurement tool in the following applications:&nbsp;</p><ul><li>Slurry beneficiation / Light element analysis&nbsp;</li><li>Product quality / Penalty costs&nbsp;</li><li>Tailings management&nbsp;</li></ul><p>Slurries include:&nbsp;</p><ul><li>Iron ore&nbsp;</li><li>Sulphur&nbsp;</li><li>Phosphates&nbsp;</li><li>Copper&nbsp;</li><li>Calcium carbonate&nbsp;</li><li>Magnesium&nbsp;</li><li>Industrial Minerals</li></ul>

News from LabRulezICPMS Library - Week 37, 2026

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Thermo Scientific Syncronis C18 Columns

Achieve repeatable and consistent liquid chromatography (LC) separations using Thermo Scientific™ Syncronis™ C18 columns. 

<p><strong>Achieve repeatable and consistent liquid chromatography (LC) separations using Thermo Scientific™ Syncronis™ C18 columns. Highly pure, high surface area silica and dense stationary phase coverage minimize secondary interactions and ensure robust, high-resolution separations.&nbsp;</strong></p><p>Double end-capping provides extra surface coverage and inertness toward basic compounds. Manufactured and rigorously tested in ISO 9000 facilities, these columns are designed to meet a range of analytical needs including fast method development, quantitative analysis, and quality control.</p><h5><strong>Highly Reproducible Separations</strong></h5><ul><li>Rigorously tested stationary phase bonded to the highest quality silica ensures consistent, predictable LC performance.</li></ul><h5><strong>Excellent Peak Shapes for Enhanced Resolution and Sensitivity</strong></h5><ul><li>Dense surface coverage of silica minimizes secondary interactions and peak tailing</li><li>Double endcapped for extra surface coverage</li></ul><h5><strong>Exceptional Column-to-Column Consistency</strong></h5><ul><li>Manufactured, packed, and tested in ISO-9000-accredited facilities</li><li>Every column individually tested to meet stringent retention, efficiency, and peak symmetry specifications</li><li>Enhanced automated packing process</li></ul><h5><strong>Available in Three Particle Sizes</strong></h5><ul><li>1.7 μm for rapid ultrahigh-performance LC (UHPLC) separations, and 3 μm and 5 μm for more traditional HPLC analysis</li></ul><h4><strong>Specifications</strong></h4><ul><li><strong>Column type:</strong> Reversed Phase</li><li><strong>Endcapped:</strong> yes</li><li><strong>Max. Pressure:</strong> 5800 psi (400 bar)</li><li><strong>Packing Material:</strong> Spherical, Fully Porous, Ultrapure Silica</li><li><strong>Stationary phase:</strong> C18</li><li><strong>USP Type:</strong> L1</li><li><strong>Surface Area:</strong> 320 m<sup>2</sup>/g</li><li><strong>Temperature:</strong> 60°C</li><li><strong>Carbon load: </strong>16%</li><li><strong>Phase:</strong> Reversed Phase</li><li><strong>Pore Size: </strong>100 Å</li><li><strong>pH: </strong>2 to 9</li></ul><h4><strong>Syncronis HPLC and UHPLC Columns</strong></h4><h5><strong>Enter a new world of chromatography</strong></h5><p>When developing a new method, one of the most important goals for the chromatographer is to achieve a consistent, reproducible separation. This makes selecting an HPLC column that offers highly-reproducible results essential to attaining this goal.</p><h5><strong>Features of Syncronis columns</strong></h5><p>Thermo Scientific Syncronis LC columns achieve high levels of consistency and reproducibility through:</p><ul><li>Highly-pure, high-surface-area silica</li><li>Dense bonding and double endcapping</li><li>Stringent manufacturing and testing protocols</li></ul>

Thermo Scientific Syncronis C18 HPLC Columns

Attain repeatable and consistent LC separations for your scale up purification needs with Thermo Scientific™ Syncronis™ C18 reversed phase preparative HPLC columns. 

<p><strong>Attain repeatable and consistent LC separations for your scale up purification needs with Thermo Scientific™ Syncronis™ C18 reversed phase preparative HPLC columns. These preparative HPLC columns have extremely pure, high surface area silica with dense stationary phase coverage to minimize secondary interactions and ensure robust, high-resolution separations. Double endcapping provides additional surface coverage and inertness toward basic compounds. Columns come in a variety of dimensions and an option for XtendedLife hardware which improves column lifetime by maintaining a uniform packed bed.</strong></p><h5><strong>Highly Reproducible Separations</strong></h5><ul><li>Rigorously tested stationary phase bonded to the highest quality silica ensures consistent, predictable LC performance.</li></ul><h5><strong>Enhanced Resolution and Sensitivity</strong></h5><ul><li>Dense surface coverage of silica minimizes secondary interactions and peak tailing.</li><li>Double endcapped for extra surface coverage.<br>C18 (USP L1) selectivity.</li></ul><p><strong>Preparative HPLC Column Hardware Options</strong> - based on column inner diameter (i.d.) and column performance needs.</p><h5><strong>Standard Threaded and Standard Flange Hardware</strong></h5><ul><li>Designed for standard applications, expertly packed and robustly designed to provide versatile products for routine use.</li><li>Standard threaded hardware for column i.d. &lt; 40mm.</li><li>Standard flange hardware for column i.d. ≥ 40mm.</li><li>Standard hardware can be modified on request to be compatible with SFC.</li></ul><h5><strong>XtendedLife Hardware</strong></h5><ul><li>Improves column lifetime by incorporating an internal Dynamic Axial Compression (DAC) system, ensuring the media bed is continuously packed tightly.</li><li>Compatible with SFC and is available in dimensions up to 50mm i.d.</li></ul><p>Preparative Guards are a proven and cost effective way to extend the lifetime of your prep column. Our preparative guard columns require the use of a preparative guard holder.</p><h5><strong>Customer Specific Orders</strong></h5><p>If there is a Thermo Scientific stationary phase you are currently using and would like to obtain in a preparative scale not shown or would like to discuss a specific column dimension, we would be happy to discuss your requirements.<br>Please contact your local sales representative for Customer Specific Orders.<br>Custom built columns are not eligible for returns.</p><h4><strong>Specifications</strong></h4><ul><li><strong>Column type:</strong> Reversed Phase</li><li><strong>Endcapped:</strong> yes</li><li><strong>Max. Pressure:</strong> 4300 psi (295 bar)</li><li><strong>Packing Material:</strong> Spherical, Fully Porous, Ultrapure Silica</li><li><strong>Stationary phase:</strong> C18</li><li><strong>USP Type:</strong> L1</li><li><strong>Surface Area:</strong> 320 m<sup>2</sup>/g</li><li><strong>Temperature:</strong> 60°C</li><li><strong>Carbon load: </strong>16%</li><li><strong>Phase:</strong> Reversed Phase</li><li><strong>Pore Size: </strong>100 Å</li><li><strong>pH: </strong>2 to 9</li></ul><h4><strong>Syncronis HPLC and UHPLC Columns</strong></h4><h5><strong>Enter a new world of chromatography</strong></h5><p>When developing a new method, one of the most important goals for the chromatographer is to achieve a consistent, reproducible separation. This makes selecting an HPLC column that offers highly-reproducible results essential to attaining this goal.</p><h5><strong>Features of Syncronis columns</strong></h5><p>Thermo Scientific Syncronis LC columns achieve high levels of consistency and reproducibility through:</p><ul><li>Highly-pure, high-surface-area silica</li><li>Dense bonding and double endcapping</li><li>Stringent manufacturing and testing protocols</li></ul>

Thermo Scientific Syncronis C8 HPLC Columns

Improve the consistency and reliability of your liquid chromatography (LC) separations using Thermo Scientific™ Syncronis™ C8 LC columns.

<p><strong>Improve the consistency and reliability of your liquid chromatography (LC) separations using Thermo Scientific™ Syncronis™ C8 LC columns. High-purity, high surface area silica and dense stationary phase coverage minimize secondary interactions and deliver reproducible, high-efficiency separations.&nbsp;</strong></p><p>Double end-capping provides extra surface coverage and inertness toward basic compounds. Manufactured and rigorously tested in ISO 9000 facilities, these columns are designed to meet a range of analytical needs including fast method development, quantitative analysis, and quality control where less retention is required than when using a C18 column.</p><h5><strong>Excellent Peak Shapes for Enhanced Resolution and Sensitivity</strong></h5><ul><li>Dense surface coverage of silica minimizes secondary interactions and peak tailing</li><li>Double endcapped for extra surface coverage</li></ul><h5><strong>Exceptional Column-to-Column Consistency</strong></h5><ul><li>Manufactured, packed, and tested in ISO-9000-accredited facilities</li><li>Every column individually tested to meet stringent retention, efficiency, and peak symmetry specifications</li><li>Enhanced automated packing process</li></ul><h5><strong>Lower Hydrophobic Retention</strong></h5><ul><li>Recommended for moderately hydrophobic analytes or for when a less hydrophobic phase provides optimum retention</li></ul><h5><strong>Available in Three Particle Sizes</strong></h5><ul><li>1.7 μm for rapid ultrahigh-performance LC (UHPLC) separations, and 3 μm and 5 μm for more traditional HPLC analysis</li></ul><h4><strong>Specifications</strong></h4><ul><li><strong>Column type:</strong> Reversed Phase</li><li><strong>Endcapped:</strong> yes</li><li><strong>Max. Pressure:</strong> 5800 psi (400 bar)</li><li><strong>Packing Material:</strong> Spherical, Fully Porous, Ultrapure Silica</li><li><strong>Stationary phase:</strong> C8</li><li><strong>USP Type:</strong> L7</li><li><strong>Surface Area:</strong> 320 m<sup>2</sup>/g</li><li><strong>Temperature:</strong> 60°C</li><li><strong>Carbon load: </strong>10%</li><li><strong>Phase:</strong> Reversed Phase</li><li><strong>Pore Size: </strong>100 Å</li><li><strong>pH: </strong>2 to 8</li></ul><h4><strong>Syncronis HPLC and UHPLC Columns</strong></h4><h5><strong>Enter a new world of chromatography</strong></h5><p>When developing a new method, one of the most important goals for the chromatographer is to achieve a consistent, reproducible separation. This makes selecting an HPLC column that offers highly-reproducible results essential to attaining this goal.</p><h5><strong>Features of Syncronis columns</strong></h5><p>Thermo Scientific Syncronis LC columns achieve high levels of consistency and reproducibility through:</p><ul><li>Highly-pure, high-surface-area silica</li><li>Dense bonding and double endcapping</li><li>Stringent manufacturing and testing protocols</li></ul>

Thermo Scientific Syncronis HILIC HPLC Columns

Ensure consistent, predictable separations of polar and hydrophilic analytes with Thermo Scientific™ Syncronis™ HILIC LC Columns. 

<p><strong>Ensure consistent, predictable separations of polar and hydrophilic analytes with Thermo Scientific™ Syncronis™ HILIC LC Columns. Highly pure, high surface area silica and dense stationary phase coverage minimize secondary interactions and deliver reproducible high-resolution separations. The zwitterionic stationary phase results in a neutral, highly polar surface and provides alternative selectivity to C18 columns without ion-pairing or derivatization. The highly organic mobile phases used with Syncronis HILIC phases facilitate efficient desolvation in ESI-MS detection and improved sensitivity.</strong></p><p>Manufactured and rigorously tested in ISO 9000 facilities, these columns are designed to meet a range of analytical needs including fast method development, quantitative analysis and quality control.</p><h5><strong>Highly Reproducible Separations</strong></h5><ul><li>Rigorously tested stationary phase bonded to the highest quality silica ensures consistent, predictable LC performance</li></ul><h5><strong>Excellent Peak Shapes for Enhanced Resolution and Sensitivity</strong></h5><ul><li>Dense surface coverage of silica minimizes secondary interactions and peak tailing</li></ul><h5><strong>Exceptional Column-to-Column Consistency</strong></h5><ul><li>Manufactured, packed, and tested in ISO-9000-accredited facilities</li><li>Every column individually tested to meet stringent retention, efficiency, and peak symmetry specifications</li><li>Enhanced automated packing process</li></ul><h5><strong>Alternative Selectivity</strong></h5><ul><li>Zwitterionic bonded phase enhances retention of polar and hydrophilic analytes</li><li>No need for ion-pair or derivatization</li></ul><h5><strong>Enhanced Sensitivity with MS Detection</strong></h5><ul><li>Highly organic mobile phase facilitates desolvation in ESI-MS</li></ul><h5><strong>Available in Three Particle Sizes</strong></h5><ul><li>1.7μm for rapid ultrahigh-performance LC (UHPLC) separations</li><li>3μm and 5μm for more traditional HPLC analysis</li></ul><h4><strong>Specifications</strong></h4><ul><li><strong>Column type:</strong> HILIC</li><li><strong>Max. Pressure:</strong> 5800 psi (400 bar)</li><li><strong>Packing Material:</strong> Spherical, Fully Porous, Ultrapure Silica</li><li><strong>Stationary phase:</strong> Zwitterionic</li><li><strong>Surface Area:</strong> 320 m<sup>2</sup>/g</li><li><strong>Temperature:</strong> 60°C</li><li><strong>Carbon load: </strong>5%</li><li><strong>Phase:</strong> HILIC</li><li><strong>Pore Size: </strong>100 Å</li><li><strong>pH: </strong>2 to 8</li></ul><h4><strong>Syncronis HPLC and UHPLC Columns</strong></h4><h5><strong>Enter a new world of chromatography</strong></h5><p>When developing a new method, one of the most important goals for the chromatographer is to achieve a consistent, reproducible separation. This makes selecting an HPLC column that offers highly-reproducible results essential to attaining this goal.</p><h5><strong>Features of Syncronis columns</strong></h5><p>Thermo Scientific Syncronis LC columns achieve high levels of consistency and reproducibility through:</p><ul><li>Highly-pure, high-surface-area silica</li><li>Dense bonding and double endcapping</li><li>Stringent manufacturing and testing protocols</li></ul>

Thermo Scientific Dionex IonPac AS11-HC IC Columns

Resolve a large number of inorganic anions and organic acid anions in complex matrices with the Thermo Scientific Dionex IonPac AS11-HC Capillary, Analytical & Guard Column.

<p><strong>Resolve a large number of inorganic anions and organic acid anions in complex matrices with the Thermo Scientific™ Dionex™ IonPac™ AS11-HC Capillary, Analytical &amp; Guard Column. Complex sample matrices such as chemical wastewater effluents and fermentation broth solutions contain a variety of inorganic anions and organic acids. With the high-capacity Dionex IonPac AS11-HC column, you can inject higher concentration samples without column overloading or peak broadening.</strong></p><p>The Dionex IonPac AS11-HC column was specifically designed to resolve analytes in a single run using a hydroxide gradient. The high-capacity column delivers improved separation for monovalent carboxylic acids including: quinate, lactate, acetate, propionate, formate, and butyrate.</p><h5><strong>High Capacity for Higher Resolution</strong></h5><ul><li>Requires longer retention times, but with higher resolution</li><li>Facilitates rapid analysis of organic acids and anions in well-characterized samples</li><li>Ideal for organic acids and anions in complex sample matrices or uncharacterized samples</li><li>Recommended for monovalent and divalent organic acids</li></ul><h5><strong>Reduce Operating Costs With Lower Eluent Requirements</strong></h5><p>The new Dionex IonPac AS11-HC Capillary column is packed with the same material as the equivalent standard bore and microbore versions (providing the same performance as a 4mm and 2mm column) using only 1% of the eluent flow rate, which helps reduce operating costs.</p><p>Use the Thermo Scientific™ Dionex™ IonPac™ ICE-AS1 or ICE-AS6 columns for organic acids in high-ionic-strength samples.</p><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 290 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 290 μeq</li><li><strong>Column Chemistry:</strong> Hydroxide</li><li><strong>For Use With (Application):</strong> Anion Exchange</li><li><strong>Ion Exchange Group: </strong>Alkanol Quaternary Ammonium Ion</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 0 to 14, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS11-HC</li><li><strong>Format:</strong> Standard Bore</li><li><strong>Packing Material: </strong>Ethylvinylbenzene/Divinylbenzene</li></ul>

Thermo Scientific Dionex IonPac AS14 IC Columns

Deliver excellent results for fast isocratic separations of inorganic anions in diverse matrices with the Thermo Scientific Dionex IonPac AS14 Carbon Eluent Anion-Exchange Column.

<p><strong>Deliver excellent results for fast isocratic separations of inorganic anions in diverse matrices with the Thermo Scientific™ Dionex™ IonPac™ AS14 Carbon Eluent Anion-Exchange Column. This universal column for the separation of inorganic anions delivers improved peak resolution and retention of fluoride in applications performed previously with the Dionex IonPac AS4A, AS4A-SC and AS12A columns, however, the Dionex IonPac AS22 Carbonate Eluent Anion-Exchange column, an advanced carbonate eluent column, is recommended for fast analysis of inorganic anions.</strong></p><h5><strong>Fast Separation of Inorganic Anions in Diverse Matrices</strong></h5><ul><li>Compliance monitoring of common anions in drinking water as specified in U.S. EPA Method 300.0 (A)</li><li>Separation of common inorganic anions in 13 min in drinking water, wastewater, food &amp; beverages, scrubber solutions, and other diverse sample matrices</li><li>Superior retention and quantification of fluoride, glycolate, acetate, and formate</li><li>Compatible with a sodium tetraborate gradient to optimize difficult separations</li><li>Solvent compatibility permits easy column cleanup after the analysis of samples with hydrophobic components.</li></ul><h5><strong>Multiple Formats Available for Application Flexibility</strong></h5><ul><li>4x250mm, 2x250mm analytical columns</li><li>4x50mm, 2x50mm guard columns</li><li>Longer 25mm columns facilitate higher resolution separations of more complex sample matrices</li><li>Smaller i.d. columns provide higher mass sensitivity, eluent and reagent conservation and lower operating costs</li></ul><p><i><strong>Note: </strong>Use with the Dionex IonPac AS14 Eluent Concentrate for simple, accurate eluent preparation.</i></p><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 65 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 65 μeq</li><li><strong>Column Chemistry:</strong> Carbonate/Bicarbonate</li><li><strong>For Use With (Application):</strong> Analysis of Fluorides and Other Inorganic Anions</li><li><strong>Ion Exchange Group: </strong>Alkyl Quaternary Ammonium</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 2 to 12, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS14</li><li><strong>Format:</strong> Standard Bore</li><li><strong>Packing Material: </strong>Ethylvinylbenzene/Divinylbenzene</li><li><strong>pH: </strong>2<strong> </strong>to 12</li></ul>

Thermo Scientific Dionex IonPac AS14A IC Columns

Thermo Scientific Dionex IonPac AS14A IC Column is high capacity anion-exchange column for fast isocratic separation of inorganic anions in environmental matrices

<p><strong>Deliver fast isocratic separation of inorganic anions from diverse and complex matrices such as drinking water, wastewater, foods and beverages, and scrubber solutions with the Thermo Scientific™ Dionex™ IonPac™ AS14A Carbon Eluent Anion-Exchange Column. The Dionex IonPac AS14A column meets or exceeds the requirements of U.S EPA Method 300.0 (A). However, the Dionex IonPac AS22 Carbonate Eluent Anion-Exchange column, an advanced carbonate eluent column, is recommended for fast analysis of inorganic anions. For the fastest separation of inorganic anions using a carbonate/bicarbonate eluent, the Dionex IonPac AS22-Fast column is recommended.</strong></p><h5><strong>Fast Separation of Inorganic Anions in Diverse Matrices</strong></h5><ul><li>Compliance monitoring of common anions in drinking water as specified in U.S. EPA Method 300.0 (A)</li><li>Separation of common inorganic anions in 8 min (3 x 150mm format) or 13 min (4 x 250mm format) in diverse sample matrices</li><li>Superior retention and quantification of fluoride</li><li>Compatible with sodium or potassium hydroxide gradient to optimize difficult separations</li><li>Solvent compatibility permits easy column cleanup after the analysis of samples with hydrophobic components.</li></ul><h5><strong>Multiple Formats Available for Application Flexibility</strong></h5><ul><li>4x250mm, 3x150mm analytical columns</li><li>4x50mm, 3x30mm guard columns</li><li>Longer 250mm columns facilitate higher resolution separations of more complex sample matrices</li><li>Shorter 150mm columns produce faster runs of relatively clean matrices</li><li>Smaller i.d. columns provide higher mass sensitivity, eluent and reagent conservation and lower operating costs</li></ul><p><i><strong>Note: </strong>Use with the Dionex IonPac AS14 Eluent Concentrate and the Combined Seven Anion Standard for simple, accurate eluent preparation.</i></p><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 65 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 120 μeq</li><li><strong>Column Chemistry:</strong> Carbonate/Bicarbonate</li><li><strong>For Use With (Application):</strong> Anion Exchange</li><li><strong>Ion Exchange Group: </strong>Alkyl Quaternary Ammonium</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 2 to 11, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS14A</li><li><strong>Format:</strong> Standard Bore</li><li><strong>pH: </strong>2<strong> </strong>to 11</li></ul>

Thermo Scientific Dionex IonPac AS15 IC Columns

Determine trace-level concentrations of inorganic anions and low-molecular-weight organic acids in high-purity water matrices with the Thermo Scientific Dionex IonPac AS15 Capillary, Analytical & Guard Columns.

<p><strong>Determine trace-level concentrations of inorganic anions and low-molecular-weight organic acids in high-purity water matrices with the Thermo Scientific™ Dionex™ IonPac™ AS15 Capillary, Analytical &amp; Guard Columns. Specifically designed for analysis of trace anions in high-purity water matrices used by the semiconductor and power generation industries, the column delivers high sensitivity and superior resolution of early-eluting anions (e.g., fluoride, glycolate, acetate, and formate). The column is optimized for selective at an operating temperature of 30°C, and it is ideal for use with large-loop injections.</strong></p><h5><strong>Available in Multiple Formats</strong></h5><ul><li>Dionex IonPac AS15-5μm (3x150mm) column for high efficiency, fast analysis (15 min)</li><li>Dionex IonPac AS15-9μm (2x250mm, 4x250mm, and 0.4x250mm) columns for higher-capacity applications</li><li>Dionex IonPac AS15 capillary column (0.4x250mm) delivers the performance of the standard bore version but requires only 1% of the eluent flow rate, which helps reduce operating costs</li></ul><h5><strong>For Best Performance</strong></h5><ul><li>Use the Thermo Scientific™ Dionex™ IonPac™ AC15 Concentrator column for ultratrace (part per trillion) analyses</li><li>Use a Dionex eluent generator for simplified eluent preparation</li><li>Use the Thermo Scientific™ Dionex™ Anion Self-Regenerating Suppressor (ASRS™ 300) or the Thermo Scientific™ Dionex™ Anion Capillary Electrolytic Suppressor (ACES™ 300) with the Dionex IonPac AS15 column for eluent suppression</li></ul><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 225 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 225 μeq</li><li><strong>Column Chemistry:</strong> Hydroxide</li><li><strong>For Use With (Application):</strong> Anion Exchange</li><li><strong>Ion Exchange Group: </strong>Alkanol Quaternary Ammonium Ion</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 0 to 14, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS15</li><li><strong>Format:</strong> Standard Bore</li><li><strong>Packing Material: </strong>Ethylvinylbenzene/Divinylbenzene</li></ul>

Thermo Scientific Dionex IonPac AS16 IC Columns

Measure trace perchlorate and other highly polarizable anions quickly and accurately in a variety of water matrices with the Thermo Scientific Dionex IonPac AS16 IC Columns.

<p><strong>Measure trace perchlorate and other highly polarizable anions quickly and accurately in a variety of water matrices with the Thermo Scientific™ Dionex™ IonPac™ AS16 IC Columns . This column simplifies the determination of polarizable anions, including thiosulfate, iodide, thiocyanate, and perchlorate using an isocratic hydroxide eluent. It is ideally suited for determination of trace perchlorate in drinking water in accordance with U.S. EPA Methods 314.0 and 314.1 (Primary Method).</strong></p><h5><strong>Designed for Simple, Sensitive Analysis</strong></h5><ul><li>Easily measure trace concentrations of perchlorate in drinking water, surface water, and ground water matrices using a large-loop injection</li><li>Separate hydrophobic anions (iodide, thiocyanate, and thiosulfate) in less than 20 min</li><li>Ideal for polyvalent anions, including polyphosphates and polycarboxylates</li><li>Ultralow hydrophobicity allows fast analysis of polarizable anions</li><li>Can be used in the second dimension of the 2D-IC method for the analysis of trace perchlorate (sub ppb) in drinking water</li></ul><h5><strong>Available in Multiple Formats</strong></h5><ul><li>Standard bore (4x250mm) and microbore (2x250mm) formats</li></ul><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 170 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 170 μeq</li><li><strong>Column Chemistry:</strong> Hydroxide</li><li><strong>For Use With (Application):</strong> Anion Exchange</li><li><strong>Ion Exchange Group: </strong>Alkanol Quaternary Ammonium Ion</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 0 to 14, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS16</li><li><strong>Format:</strong> Standard Bore</li><li><strong>Packing Material: </strong>Ethylvinylbenzene/Divinylbenzene</li></ul>

Thermo Scientific Dionex IonPac AS17-C IC Columns

Quickly determine common inorganic anions in high-purity water matrices with the Thermo Scientific Dionex IonPac AS17-C column. 

<p><strong>Quickly determine common inorganic anions in high-purity water matrices with the Thermo Scientific™ Dionex IonPac AS17-C column. This low-capacity column is optimized for fast gradient separation of inorganic anions in simple sample matrices. It is also ideal for fast gradient separation of sulfur species, including sulfite, sulfate, and thiosulfate. The Dionex IonPac AS17C column is the recommended replacement for all Dionex IonPac AS17 column anion applications.</strong></p><h5><strong>Make Gradient Separations as Easy as Isocratic Runs</strong></h5><p>The Dionex IonPac AS17-C column is designed to be used in conjunction with the Dionex Eluent Generator. The Dionex Eluent Generator automatically produces potassium hydroxide eluents from water, making gradient separations as easy as isocratic runs. Using the Dionex Eluent Generator under gradient conditions, common inorganic anions can easily be separated in a variety of sample matrices including high purity water, drinking water, wastewater, process streams, and scrubber solutions.</p><h5><strong>Achieve Superior Chromatographic Performance</strong></h5><ul><li>Fast gradient separation of inorganic anions in high purity water matrices</li><li>Easy suppression of hydroxide eluent to a very low background with the Thermo Scientific™ Dionex™ Anion Self-Regenerating Suppressor (ASRS™ 300) for trace level determinations (including fluoride) even with a large loop injection</li><li>Superior retention and quantification of fluoride, acetate, propionate, and formate</li><li>Meets performance requirements specified in U.S. EPA Method 300.0 (A)</li><li>Operates at ambient or elevated temperatures</li><li>Column selectivity is optimized for operating temperature of 30°C to ensure reproducible results</li><li>Compatible with Reagent-Free™ Ion Chromatography (RFIC™) systems</li><li>Compatible with organic solvents to enhance analyte solubility, modify column selectivity, or for effective column clean-up</li></ul><p><strong>Note:</strong><i> The Thermo Scientific™ Dionex™ IonPac™ AS18 column is the recommended hydroxide-selective column for determination of common anions in diverse sample matrices.</i></p><h4><strong>Specifications</strong></h4><ul><li><strong>Anion Exchange Capacity:</strong> 30 μeq</li><li><strong>Crosslinking: </strong>55% DVB</li><li><strong>Column Capacity:</strong> 30 μeq</li><li><strong>Column Chemistry:</strong> Hydroxide</li><li><strong>For Use With (Application):</strong> Anion Exchange</li><li><strong>Ion Exchange Group: </strong>Alkanol Quaternary Ammonium Ion</li><li><strong>Max. Pressure:</strong> 4000 psi (275 bar)</li><li><strong>Solvent Compatibility:</strong> pH 0 to 14, 0 to 100% HPLC Solvents</li><li><strong>Stationary phase:</strong> IonPac AS17-C</li><li><strong>Format:</strong> Standard Bore</li><li><strong>Packing Material: </strong>Ethylvinylbenzene/Divinylbenzene</li></ul>

Products from category HPLC columns - page 7

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