Conexiant
Login
  • The Analytical Scientist
  • The Cannabis Scientist
  • The Medicine Maker
  • The Ophthalmologist
  • The Pathologist
  • The Traditional Scientist
The Analytical Scientist
  • Explore

    Explore

    • Latest
    • News & Research
    • Trends & Challenges
    • Keynote Interviews
    • Opinion & Personal Narratives
    • Product Profiles
    • App Notes

    Featured Topics

    • Mass Spectrometry
    • Chromatography
    • Spectroscopy

    Issues

    • Latest Issue
    • Archive
  • Topics

    Techniques & Tools

    • Mass Spectrometry
    • Chromatography
    • Spectroscopy
    • Microscopy
    • Sensors
    • Data and AI

    • View All Topics

    Applications & Fields

    • Clinical
    • Environmental
    • Food, Beverage & Agriculture
    • Pharma and Biopharma
    • Omics
    • Forensics
  • People & Profiles

    People & Profiles

    • Power List
    • Voices in the Community
    • Sitting Down With
    • Authors & Contributors
  • Business & Education

    Business & Education

    • Innovation
    • Business & Entrepreneurship
    • Career Pathways
  • Events
    • Live Events
    • Webinars
  • Multimedia
    • Video
Subscribe
Subscribe

False

The Analytical Scientist / App Notes / 2013 / Detailed hydrocarbon analysis

Detailed hydrocarbon analysis

07/03/2013

Share

Featured Image
Introduction

Detailed hydrocarbon analysis (DHA) is a separation technique used by a variety of laboratories involved in the petrochemical industry for analysis and identification of individual components as well as for bulk hydrocarbon characterisation of a particular sample. Bulk analysis looks at gasoline composition in terms of PONA components (Paraffins, Olefins, Naphthalenes and Aromatics) and other fuels in the C1-C13 range since this gives an indication of overall quality of the sample.

Logo of peak
The analysis of gasoline for spark ignition components is essential for quality control. Owing to the complex nature of gasoline samples, good resolution between eluents is required and therefore a long column is used (typically 100m). Several methods are routinely used for DHA which differ in their oven temperature ramp rates or in the length of column used. Each method has its advantages and disadvantages since some improve peak resolution of low boiling compounds whereas others provide better resolution of heavier compounds at the end of the chromatogram. The complex nature of the methodology coupled with the use of such a long column means that run times can easily exceed 120 minutes when using helium carrier gas. However, the use of hydrogen can vastly increase run rates because of its efficiency at higher linear velocities. This is a particularly attractive prospect for oil analysis laboratories since faster throughput of sample means increased profitability. The benefits of using hydrogen in terms of improved chromatography combined with the increasing cost of helium along with supply issues means that laboratories switching from helium to hydrogen can become much more profitable whilst maintaining standards of analysis that conform to industry standards.This application note demonstrates a comparison of gasoline analysis using helium carrier gas following ASTM method D67291 and the use of unfiltered hydrogen carrier gas produced by a Peak Scientific Precision Trace hydrogen generator in DHA following ASTM method D6729-1 appendix X22 and demonstrates the improvement in run time whilst maintaining crucial separations between certain components.
Results and Discussion
Detailed hydrocarbon analysis of gasoline showed that the elution time of the last compound in the mixture, n-Pentadecane, could be reduced from 125 minutes to less than 74 minutes by switching carrier gas from helium to hydrogen (figure 1). Despite the difference in analysis times, the PONA analysis showed that quantitative differences were not significantly different when using either carrier gas (table 1). Despite the much higher carrier gas flow rates when using hydrogen carrier gas, critical separations were still achieved in most cases and in certain cases were even improved. Separation of 1-methylcyclopentene and benzene, which is highly regulated analysis because of the importance of the benzene fraction, was actually improved when using hydrogen carrier gas despite the quicker elution times of the compounds with hydrogen as a carrier gas (figure 2). Separation of Toluene and 2,3,3-Trimethylpentane was achieved using helium whereas with hydrogen the two compounds co-eluted (figure 3. To separate these two compounds using hydrogen carrier gas some improvements to the method would need to be made. Separation of Tridecane and 1-methylnaphthalene was achieved equally well using both carrier gases (figure 4).The results of the DHA show that the use of hydrogen as a carrier gas, following ASTM D6729 appendix 2 methodology can vastly reduce analysis times for gasoline analysis whilst providing the necessary resolution required for separations of critical components.
Figure 1Figure 1. Comparison of DHA of total gasoline sample using hydrogen and helium.
Figure 2Figure 2. Comparison of separation of 1-methylcyclopentene and benzene when using hydrogen and helium as carrier gas.
Figure 3.Figure 3. Comparison of separation of Toluene and 2,3,3-Trimethylpentane when using hydrogen and helium as carrier gas.
Figure 4. Figure 4. Comparison of separation of Tridecane and 1-methylnaphthalene when using hydrogen and helium as carrier gas.
Table 2.Table 2. Quantitative results of PONA compounds.

>> Download the full Application Note as PDF

Newsletters

Receive the latest pathologist news, personalities, education, and career development – weekly to your inbox.

Newsletter Signup Image

Explore More in Pathology

Dive deeper into the world of pathology. Explore the latest articles, case studies, expert insights, and groundbreaking research.

False

Advertisement

Recommended

False

Related Content

Extraction of Multiple Mycotoxins From Grain Using ISOLUTE<sup>®</sup> Myco prior to LC-MS/MS Analysis
Extraction of Multiple Mycotoxins From Grain Using ISOLUTE<sup>®</sup> Myco prior to LC-MS/MS Analysis

April 25, 2013

This application note describes a Solid Phase Extraction (SPE) protocol for the extraction of a range of mycotoxins from wheat flour, wheat, maize and barley using ISOLUTE® Myco with LC-MS/MS...

Analysis of 18 Polycyclic Aromatic Hydrocarbons in Soil Using the QuEChERS Method
Analysis of 18 Polycyclic Aromatic Hydrocarbons in Soil Using the QuEChERS Method

April 29, 2013

The use of QuEChERS dispersive SPE as a simple, fast, and quantitative sample preparation method is demonstrated for the GC-MS analysis of 18 polycyclic aromatic hydrocarbons (PAHs) in soil...

Analysis of Low Level Pyrethroid Pesticides in Water
Analysis of Low Level Pyrethroid Pesticides in Water

April 29, 2013

A method for the determination of pyrethroids in water at ultra-low-level concentrations of 0...

Determination of Phthalates in Drinking Water by UHPLC with UV Detection
Determination of Phthalates in Drinking Water by UHPLC with UV Detection

April 29, 2013

To develop an efficient high-performance liquid chromatography (HPLC) method for the simultaneous determination of 19 phthalate compounds in drinking water...

False

The Analytical Scientist
Subscribe

About

  • About Us
  • Work at Conexiant Europe
  • Terms and Conditions
  • Privacy Policy
  • Advertise With Us
  • Contact Us

Copyright © 2025 Texere Publishing Limited (trading as Conexiant), with registered number 08113419 whose registered office is at Booths No. 1, Booths Park, Chelford Road, Knutsford, England, WA16 8GS.