CromSil™ PAH

Polycyclic Aromatic Hydrocarbon Column

A high-selectivity reversed-phase HPLC column for PAH analysis, separating all 16 EPA priority PAHs with exceptional resolution and speed.

Overview

CromSil™ PAH is a specialty HPLC column engineered for the analysis of polycyclic aromatic hydrocarbons (PAHs), a group of environmental contaminants and food-processing byproducts known for their multiple fused aromatic rings and potential carcinogenicity​. PAHs such as naphthalene, benzo[a]pyrene, and chrysene are notoriously difficult to separate due to their similar structures and hydrophobic nature. This column directly addresses that problem: it provides a highly efficient and reliable means to resolve the 16 EPA priority pollutant PAHs in a single chromatographic run​. The purpose of CromSil™ PAH is to enable laboratories (environmental, petrochemical, food safety) to detect and quantify PAHs in samples like water, soil, air particulates, or grilled foods with confidence and in compliance with regulatory methods. Traditional C18 columns might struggle with co-elution of certain PAH isomers or require long run times – CromSil™ PAH solves this with a tailored stationary phase that enhances shape selectivity and retention for aromatic compounds, thus achieving baseline separation in shorter analysis times (often under 20 minutes for the full PAH suite​). In summary, this product offers scientific precision through a purpose-built phase for PAHs (ensuring even difficult isomer pairs are separated) and commercial persuasiveness by improving throughput and data quality for PAH testing labs.

Technology Background

CromSil™ PAH is based on a high-purity silica platform with a specialty C18 bonding that is optimized for aromatic, planar compounds. The column’s stationary phase is a large-pore (approximately 300 Å) silica, which accommodates the relatively bulky PAH molecules and allows them to interact fully with the stationary phase​ The C18 chains are bonded in a way that provides a degree of shape selectivity – often referred to as a “polymeric” bonding or multi-layer bonding – and the phase is not endcapped​ This means some silanol groups remain accessible. Counterintuitively, this is beneficial for PAH separations: the slight secondary interactions and the specific morphology of the bonded phase help differentiate PAHs not just by hydrophobicity but also by molecular shape (planarity) and size. This technology is reminiscent of well-known PAH-specific columns (for example, the legacy Vydac 201TP series) which set the standard for PAH analysis​

Thanks to this design, CromSil™ PAH can separate all EPA 16 priority PAHs with baseline resolution, including challenging isomeric pairs such as benzo[b]fluoranthene vs benzo[k]fluoranthene and chrysene vs benzo[a]anthracene, which have identical molecular weights and very similar structures​​ The column is optimized for use with common PAH analytical methods – typically a gradient reversed-phase method using water and acetonitrile (or methanol) as mobile phases. It is built to withstand the high organic content (often reaching 100% acetonitrile) and the high flow rates used to speed up PAH analysis. Chrom Science & Technology’s technology for this column specifically notes that it can achieve the separation of 16 PAHs in under 20 minutes when using an appropriate fast gradient​ The large pore and moderate carbon load (~8–9% C) ensure that even high molecular weight PAHs (like Indeno[1,2,3-cd]pyrene) elute without excessive tailing or overly long retention​ Additionally, the phase shows low bleed and excellent stability, which is important for fluorescence or MS detection commonly employed for PAHs. In essence, the technology behind CromSil™ PAH is a refined C18 phase with enhanced pi-pi interaction capacity and shape selectivity, enabling it to outperform conventional columns for aromatic hydrocarbon separations and meet stringent regulatory method criteria (EPA methods 550.1, 610, 8310, etc.)​

Technical Specifications

  • Phase and Bonding: Specially bonded C18 on ultra-high purity silica, designed for PAH selectivity. Bonding type is polymeric C18 (multiple ligand layers), yielding a phase with approximately 8% carbon load and minimal endcapping​ This leaves slight silanol activity to enhance selectivity for polyaromatic structures. The silica support has a 300 Å pore size and relatively low surface area (~70–90 m²/g)​, matching the needs of large, planar PAH molecules (which prefer wide pores to avoid diffusion hindrance).
  • Particle Size: 5 µm (analytical grade). The column is available in 3 µm for high-speed UHPLC applications as well, and larger particles (7 or 10 µm) for preparative scales, but 5 µm is the standard for analytical PAH work balancing efficiency and pressure. Particles are spherical and uniformly packed for high plate counts (~>8000 plates for a 150 mm column on test PAHs).
  • Column Dimensions: 150 mm × 4.6 mm ID is the typical configuration for standard PAH analysis (it allows the full 16 PAH separation within ~15–20 min under gradient)​​ Also available in 250 mm length for even higher resolution or to accommodate isocratic methods, and shorter 100 mm length for ultrafast analysis (where some resolution might be traded for speed). Guard columns (10 mm × 4.6 mm) are recommended to protect against particulate matter from environmental samples. All hardware is stainless steel, rated to >400 bar, to handle high organic solvents and fast flow gradients.
  • Operating Conditions: Typically used with a binary gradient of water (often with a small % of organic modifier) and acetonitrile (or methanol) – many standard methods start at ~50% ACN and ramp to 100% ACN​ The column is stable in 100% organic. Temperature can be ambient (20–30°C); some methods use ~30°C to improve consistency. Flow rates of 1.0–1.5 mL/min on a 4.6 mm ID are standard, and the column is capable of that flow due to the 5 µm particles. The column is compatible with UV (254 nm) detection (common for PAHs), as well as fluorescence detection for enhanced sensitivity (sequential programming of excitation/emission per PAH). It exhibits low baseline noise on both UV and fluorescence due to the high purity of silica (low bleed).
  • Selectivity & Capacity: The selectivity is tuned for PAHs: lighter PAHs (2–3 rings like naphthalene, fluorene) elute early, while heavy PAHs (5–6 rings like benzopyrenes, indeno-pyrene) retain strongly but still elute within a reasonable window, typically under 15 minutes in a gradient​​ The column’s loading capacity for PAHs is high enough to handle environmental extracts – typically one can inject e.g. 100 µL of a soil extract concentrate (if using a 150 mm column) without overload, as PAHs are usually in ng/mL levels. It also handles the solvent-rich injections (like PAHs often dissolved in acetone or acetonitrile) without issue.
  • Regulatory Conformance: CromSil™ PAH’s performance aligns with EPA methods such as 610 and 8310 which specify a special PAH column. In fact, those methods historically reference columns like Supelcosil LC-PAH or Vydac PAH columns; CromSil™ PAH is an equivalent or superior alternative, capable of meeting or exceeding the required resolution criteria for those methods​ Quality control tests for each column batch include separation of a PAH mix to ensure resolution of key pairs (e.g., baseline separation of chrysene/benz[a]anthracene pair) and tailing factor limits.
  • Durability: Even though this is a silica-based column, it is used in benign pH (mostly neutral to slightly acidic organic-water mixes) and so exhibits long lifetime. It’s recommended to flush the column with 100% organic after use (to prevent any residue build-up) and store in acetonitrile. The bonding is stable and won’t hydrolyze under typical PAH analysis conditions. Customers can expect many dozens of sample injections (including complex extracts) before any noticeable performance drop, especially if a guard column is used for dirty samples.

Key Features & Benefits

  • Complete EPA 16 PAH Separation: CromSil™ PAH is proven to separate all 16 EPA priority pollutant PAHs to baseline resolution​​ This includes notoriously difficult separations like the triplet of benzo[b], benzo[k]fluoranthene and benzo[a]pyrene, and the chrysene/benz[a]anthracene pair. With this column, labs can be confident that each target PAH peak is resolved and quantified accurately without interference – a critical requirement for regulatory reporting and risk assessment. The ability to achieve this in one analysis streamlines workflows and ensures data integrity.
  • Fast Analysis Times: Thanks to optimized phase chemistry and efficient mass transfer, CromSil™ PAH can execute the full analysis in under 20 minutes​(using a 150 mm column and a fast gradient). This high speed means higher sample throughput for busy labs – environmental labs, for instance, can run more samples per day for PAH monitoring. Rapid run times also reduce solvent consumption and operating cost. Even when using a longer 250 mm column for maximum resolution, the column’s performance allows aggressive gradients to still keep run times around 30 minutes or less, which is faster than many conventional C18 solutions.
  • Enhanced Shape Selectivity: The specially engineered C18 phase exhibits shape selectivity, meaning it discriminates between PAH molecules not just by size but also by shape (planarity vs angularity)​ This results in very distinct elution orders that match the needs of PAH analysis. For example, it spreads out isomeric PAHs that might co-elute on a standard ODS column. Users benefit by getting symmetrical, well-resolved peaks even for compounds that are very similar – an advantage when identifying and quantifying PAHs in complex mixtures (like an environmental sample with many PAH isomers). This feature is a direct result of the polymeric bonding and pore structure, and it translates into superior separation power.
  • High Detection Sensitivity Compatibility: Many PAH analyses use fluorescence detection for better sensitivity. CromSil™ PAH is designed with extremely low background bleed and minimal noise, making it ideal for fluorescence and even LC-MS detection of PAHs. The column doesn’t introduce interfering peaks or elevated baseline, so the inherent sensitivity of detectors can be fully utilized. For instance, trace-level PAHs in drinking water (sub-ng/L levels) can be measured after extraction using this column plus fluorescence detection – the sharp peaks and low noise floor improve limits of detection. For labs doing food safety (e.g., PAHs in edible oils or grilled meats), this means even carcinogens at ppb levels are reliably picked up.
  • Trusted Method Alignment: Using CromSil™ PAH gives laboratories a column that aligns with well-established methods and industry practices. As SepaChrom notes, their PAH phase (Vydamas PAH) was developed to meet current and future environmental regulations​ This column has the same pedigree – it effectively emulates or exceeds the performance of classic PAH-specific columns (like Vydac® 201TP) which have been references in EPA and ISO methods. Thus, adopting CromSil™ PAH involves minimal method re-validation if switching from another PAH column, and it provides confidence to auditors or clients that the lab is using an appropriate “PAH designated” column for compliance monitoring.
  • Broad Application Range: While targeted at the EPA 16, this column can also separate other PAHs and related aromatic compounds. It has been used beyond just environmental samples – for example, in petrochemical analysis (to profile polyaromatics in oils), and in food safety (for the EU 15+1 PAH list). Its robust aromatic selectivity means it can handle any complex mixture of aromatic hydrocarbons. This versatility means a lab can use the one column for various PAH methods: whether it’s water testing, soil extract analysis, or checking PAHs in packaging materials. It’s also capable of handling high concentrations (with appropriate calibration), which is useful for sources like coal tar or diesel extracts where PAHs are abundant and need dilution. In all cases, the column’s performance ensures that results are reliable and reproducible.

Application Segments

CromSil™ PAH serves a critical role in a range of fields concerned with PAH contamination and analysis:

  • Environmental Monitoring: The column is indispensable for water quality labs analyzing PAHs in drinking water, groundwater, and wastewater per EPA or EU regulations. It cleanly separates the priority pollutants so that each can be quantified to ensure levels are below regulatory limits​ Similarly, in soil and sediment analysis, after sample extraction (e.g., EPA 3540 Soxhlet or QuEChERS for soil), CromSil™ PAH provides the separation needed to identify the PAHs present in contaminated sites (such as former gasworks, creosote-treated areas, or Superfund sites). Air quality labs also use it to analyze PAHs collected on filters (PM2.5 or PM10 samples), checking compounds like benzo[a]pyrene that are indicators of combustion pollution. The column’s reliability and speed greatly assist in high-volume monitoring programs.
  • Food Safety and Packaging: PAHs can enter foods through smoking, grilling, or environmental deposition. CromSil™ PAH is utilized by food safety laboratories to test oils, smoked meats, fish, and cereals for PAH content. For example, EU regulations stipulate limits for the sum of certain PAHs in food; this column helps measure those with the required sensitivity and separation. It can differentiate PAHs even in complex fatty matrices when coupled with proper sample prep (solid-phase extraction, etc.). Additionally, it’s used to analyze materials in contact with food (like polynuclear aromatic content in food packaging inks or recycled cardboard) to ensure they don’t leach PAHs. The column’s high resolution prevents false positives (no overlapping peaks that could be misidentified) – critical for consumer safety reports.
  • Petrochemical and Oil Industry: Refineries and petrochemical labs employ CromSil™ PAH to characterize petroleum products. For instance, it can separate PAHs in lubricant base oils or extender oils used in tires (there are EU limits on PAHs in tire oils). In the petrochemical context, knowing the PAH profile of a product helps in quality control and regulatory compliance (like REACH regulations). The column’s ability to handle heavy aromatic mixtures and still produce a clear chromatogram is particularly useful here. It’s also used in research to examine combustion byproducts or to study the efficiency of PAH removal in oil processing.
  • Academic & R&D (Environmental Chemistry): Researchers studying the fate and transport of PAHs in the environment (in soils, rivers, or air) rely on such a column to get detailed PAH speciation. CromSil™ PAH would be a key tool in any study measuring how PAHs degrade or persist, since you need to see each compound’s concentration over time. Its robust performance lets researchers focus on data interpretation rather than worrying about chromatographic issues. The same applies to toxicology studies: if scientists are exposing cell cultures or organisms to PAH mixtures, they’ll need to verify the composition of their exposure mixtures – this column can separate the mixture to ensure they know exactly what and how much of each PAH was present, lending accuracy to dose-response assessments.
  • Forensic Science: In forensic analysis of fires or spills, identifying PAH patterns can point to sources of pollution or combustion (for example, pyrogenic vs petrogenic PAH sources have different profiles). CromSil™ PAH can be used to generate these profiles from residues, helping forensic chemists determine if PAHs come from a petroleum spill, a coal tar, or a burn event. It provides the fine resolution needed to compare against reference PAH ratios. This can be crucial evidence in environmental litigation or contamination source apportionment.
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