an introduction to aliphatic and aromatic tph analysis by ... - gcxgc presentation 2015...
TRANSCRIPT
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Scientific Analysis Laboratories Ltd
An Introduction to Aliphatic and Aromatic TPH analysis by two
dimensional GC / FID
David Smith, Technical Director
Scientific Analysis Laboratories Ltd
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Scientific Analysis Laboratories Ltd
Aliphatic and Aromatic TPH – A New Dimension !
● A requirement of environmental fate and risk analysis is the separation of aliphatic from the aromatic hydrocarbons
● Further breakdown to carbon banding chain lengths
● The volatile fraction (C5-C
10) is analysed by GC/MS (headspace), where the aromatics
can be identified and quantified individually and hence separated from the aliphatics using Mass Spectrometry and selected ions
● For years, the separation of aliphatic and aromatic fractions in the extractable fraction (C
10-C
40) has involved the use of a physical bench top separation technique such as Solid
Phase Extraction (SPE)
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TPH CWG
● Measuring the total concentration of petroleum hydrocarbons (TPH) in soil does not give a useful basis for the evaluation of the potential risks to man and the environment
● Hydrocarbon fractions divided into aliphatic and aromatic fractions and supplemented by analysis of single compounds. This will be a much more useful basis for carrying out risk assessments
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Criteria Working Group
The "Total Petroleum Hydrocarbon Criteria Working Group (TPHCWG)" was formed in the USA in 1993 with the goalto develop scientifically defensible information for establishing soil clean up levels that are protective of human health at hydrocarbon contaminated sites. The group had more than 400 participants from the oil industry, consultant, several state governments and the US EPA. The group has published 5 reports encompassing their findings and their recommendations:
Vol-1- Analysis of Petroleum hydrocarbons in Environmental mediaVol-2- Composition of Petroleum mixturesVol-3- Selection of TPH fractionsVol-4- Fraction specific classes and reference concentrationsVol-5- Risk evaluation
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Risk based Approach
Two sites may have TPH measurements of 500 ppm but constituents at one site may include carcinogenic compounds while these compounds may be absent at the other site The risk at a specific site will change with time as contaminants evaporate,dissolve, biodegrade, and become sequestered
A valid correlation between TPH and risk would have to be site- and time-specific, related to a single spill, and, even then, the correlation might not be the same around the periphery of a plume where the rate of compositional change accelerates
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CWG FractionsThe American Petroleum Institute (API) that found it necessary to modify the method slightly to incorporate evaluation of heavierpetroleum fractions. This resulted in a suggestion to prolong the highest fraction (from EC35 to EC44 ), where aromatics and aliphatics are assessed separately, and add an even heavier fraction (EC44+ ) that includes both aliphatics and aromatics
Aliphatic fractions>5 to 6>6 to 8>8 to 10>10 to 12>12 to 16>16 to 21>21 to 35>35 to 44
Aromatic fractions>5 to 7>7 to 8>8 to 10>10 to 12>12 to 16>16 to 21>21 to 35>35 to 44
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CWG Fractions
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Equivalent Carbon Numbers
.The Equivalent Carbon Number, EC, is related to the boiling point of a chemicalnormalized to the boiling point of the n-alkanes or its retention time in a boilingpoint gas chromatographic (GC) column
Hexane contains six carbons and has a boiling point of 69o C. Its equivalent carbon number is six. Benzene, also containing six carbons, has a boiling point of 80o C. Based on benzene’s boiling point and its retention time in a boiling point GC column, benzene’s equivalent carbon number is 6.5
This approach is consistent with methods routinely used in the petroleum industry for separating complex mixtures and is standard for CWG analysis
Note that for molecules with higher relative carbon number indices, the disparity between aliphatic and aromatic hydrocarbons is great (see next two slides)
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Equivalent Carbon Numbers
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Equivalent Carbon Numbers
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Hydrocarbons get into the environment !
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Biodegradation
Biodegradation processes can be very complex: The extent of biodegradation is dependent on many factors including:● The type of microorganisms present● Environmental conditions (temperature, oxygen levels, moisture etc.) ● Predominant hydrocarbon types● Bioavailability of hydrocarbon contaminants n-Alkanes biodegrade rapidly with branched alkanes and single saturated ring compounds degrading more slowly
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Environmental Fate Soil - weathering
Petroleum products released into the environment undergo weathering processeswith time. These processes include:● Evaporation● Leaching (transfer to the aqueous phase) through solution and entrainment (physical transport along with the aqueous phase)
● Chemical oxidation● Microbial degradation (Christensen and Larsen, 1993) The rate of weathering is highly dependent on environmental conditions.For example: gasoline, a volatile product, will evaporate readily in a surfacespill, while gasoline released below 10 feet of clay topped with asphalt will tend to evaporate slowly
Evaporative processes are very important in the weathering of volatile petroleum products, and may be the dominant weathering process for gasoline
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Environmental Fate .
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Environmental Fate – Waters - Leaching
Leaching processes introduce hydrocarbon into the water phase by solubilityand entrainment. Aromatics, and especially BTEX, tend to be the most water soluble fraction of petroleum Petroleum contaminated groundwater tends to be enriched in aromatics relative to other petroleum constituentsRelatively insoluble hydrocarbons may be entrained in water through adsorption into kaolinate particles suspended in the water or as an agglomeration of oil droplets (micro-emulsion)
In cases where groundwater contains only dissolved hydrocarbons, it may NOT be possible to identify the original petroleum product because only a portion of the free product will be present in the dissolved phase. As whole product floats on groundwater, the free product will gradually lose the water-soluble compounds. Whole products have highly distinctive GC fingerprints relative to water-soluble fractions. Groundwater containing entrained product will have a GC fingerprint that is a combination of the free product chromatogram plus enhanced amounts of the soluble aromatics
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Associated Quality in the Analysis
Validation 11x2 by 3 matrices + CRM'sQuality Contol charts – Spiked LRM'sSystem Suitability ControlsOngoing Calibration checks every 19Blanks (reagent blanks method blanks, Trip blanks)Multipoint CalibrationsProficiency Testing Contest / Aquacheck / RTCMCERTSUKAS
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Scientific Analysis Laboratories Ltd
Historical Aliphatic / Aromatic separation technique.
Solid phase extractionSample extracted in organic solventCartridge conditionedAliphatic fraction collectedAromatic fraction collectedConcentrationAnalysis
DrawbacksBreakthroughMore stages for errors to occurReproducibilityInterferencesFraction losses
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Scientific Analysis Laboratories Ltd
What is two dimensional GC and how it works
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What is two dimensional GC and how it works● Separation of complex compounds without the need of bench top techniques such as SPE● Two columns working in series● First column separating by boiling point● Second column separating by polarity● Controlled by a Modulator● Ideal for use with an FID
Advantages over conventional GC
● No physical split, no losses occur and a 100% split is achieved● No 'breakthrough' can occur and variances in SPE cartridges and their
conditioning are a thing of the past, ensuring that data is more consistent,
reliable and reproducible● Multi stage, error prone preparation steps are negated
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What The following slides will show......
● Sets of standards showing how 2 dimensions are better than one
● Real life samples what they look like performed this way
● Comparison of new chromatograms against 'old'
● Examples of interferences encountered in the conventional method and how GCxGC counteracts these
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443743-017 total TPH chromatogram
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443743-017 Cartridge split method
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443743-017
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Aliphatic only
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Ali / Aro Standard
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Aliphatic and Aromatic compounds
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Kerosene
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Diesel
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Lube Oil
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493659-009
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493659-009
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493659-009
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493659-009
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493659-009
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493659-009
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493659-009
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Positioning Standard
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493659-009
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438161-001
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432682-060
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Humic acids
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445758-001 Humic Acids
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All Humic Acids (tail view)
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Mineral oil humic acid mix (tail view)
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Phenolic compounds (tail view)
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Aliphatic and Aromatic TPH analysis by two dimensional GC / FID
●100% recovery●Guaranteed split●More accurate and reliable results●Able to deal with interferences better●Far better chromatographic resolution
Thank you