Determination of Benzene and Toluene in Gasoline by ASTM D3606 on an Agilent 8890 GC with Capillary Columns

Determination of Benzene and Toluene in Gasoline by ASTM D3606 on an Agilent 8890 GC with Capillary Columns

Application Note Energy and Chemicals Determination of Benzene and Toluene in Gasoline by ASTM D3606 on an Agilent 8890 GC with Capillary Columns Author Abstract Ian Eisele Agilent Technologies, Inc. In accordance with ASTM D3606, the concentration of benzene and toluene in finished gasoline was determined on an Agilent 8890 gas chromatograph. This study used capillary columns and a midcolumn backflush with a monitor channel to ease with the setup of the backflush. This Application Note also demonstrates the use of hydrogen as an alternate carrier gas. Introduction with the peaks of interest on the polar The length and internal diameter of analytical column. To prevent this this segment were designed to match The determination of benzene and interference, the use of backflush in this the flow rate of the analytical column, toluene concentrations in gasoline is application is essential to the separation column 2. Since the flows for columns 2 necessary for regulatory and blending of the peaks of interest from the complex and 3 are the same, the effluent from purposes. In 2007, the Environmental matrix of gasoline. column 1 is split equally between the Protection Agency (EPA) published analytical column and the monitor regulations to reduce the emission of Experimental channel. Compounds quickly elute from benzene from mobile sources, which the short segment of fused silica to the included controls on passenger vehicles. Instrumentation second FID. This enables monitoring of The Control of Hazardous Air Pollutants Figure 1 presents a schematic of this compounds eluting from the precolumn from Mobile Sources final rule took configuration. A 30 m HP-1ms Ultra with a very short time delay, simplifying effect in 2011, limiting the annual refinery Inert precolumn is used for the initial the determination of the backflush average for benzene in gasoline to 0.62% separation of hydrocarbons while a time. Using a PSD also allows an by volume.1 60 m DB-WAXetr analytical column easier implementation of a backflush This Application Note follows is used to separate aromatic and configuration, thanks largely to its built-in 3 ASTM D3606-17, Standard Test aliphatic compounds. Between these purge flow. two columns is a purged two-way Method for Determination of Benzene Chemicals and standards and Toluene in Spark Ignition Fuels by splitter with purge gas supplied from a A seven-level calibration standard was Gas Chromatography, procedure A.2 pneumatic switching device (PSD) to purchased from AccuStandard. The This method uses capillary columns allow backflushing. The other outlet from concentration ranges for benzene and in place of the packed columns used the two-way splitter is connected to the toluene were 0.06 to 5% by volume and in procedure B. The use of capillary second FID as a monitor channel. 0.5 to 20% by volume, respectively. The columns provides improved separation The inclusion of the monitor channel internal standard was methyl isobutyl of benzene from oxygenates such as takes some of the guesswork out of ketone (MIBK) at 4% by volume. The ethanol and butanol. A method based on backflushing. This monitor channel, lowest concentration level was used capillary columns also runs the carrier column 3, consists of a very short for the determination of benzene’s gas at a reduced flow rate compared segment of deactivated fused silica. signal-to-noise (S/N). to the packed column method. D3606 procedure B recommends up to 44 mL/min carrier flow, so switching to a capillary column-based method can immediately reduce gas consumption. SSL PSD An 8890 GC was equipped with a mixed-phase column set with midcolumn backflush and two flame ionization detectors (FIDs). Commonly, FID1 backflushing is performed using two segments of the same analytical column, which maintains elution order throughout Column 2 the analysis. Unwanted compounds can be backflushed through the precolumn Column 1 before they enter the analytical column, FID2 offering improved column lifetime and reduced cycle time. In this analysis, compounds that elute after toluene on Column 3 the nonpolar precolumn will interfere Figure 1. Schematic diagram of an Agilent 8890 GC configured for D3606. Column 1 is a 30 m HP-1ms Ultra Inert. Column 2 is a 60 m DB-WAXetr. Column 3 is a short segment of deactivated fused silica. 2 Neat solvents were used to prepare the the method translator was set to a helium to hydrogen carrier gas for backflush timing and resolution mixture speed gain of 1.0 instead of the translate the analytical column. Table 1 shows (>99.99% purity, Sigma-Aldrich). This option. This causes the translation the final translated column flow for mixture was composed of 1% benzene, software to retain the original method’s hydrogen carrier gas. Running with these 20% toluene, 4% MIBK, and 20% ethanol holdup time/void time for the translated parameters resulted in a chromatogram by volume in isooctane. Regular method. Figure 2 demonstrates the with very similar retention times for the unleaded gasoline was purchased from a setup for translating the method from peaks of interest (Figure 3). local gas station. The gasoline samples were prepared by adding 1 mL of MIBK to a 25 mL volumetric flask filled to the mark with the gasoline sample. Results and discussion Method translation ASTM D3606-17 only includes parameters for the use of helium as a carrier gas; however, the use of hydrogen in place of helium as the carrier gas is a quick and easy way to save on gas supply costs. This application is perfectly suited for the use of hydrogen as an alternative carrier gas, and the 8890 GC includes several safety features to reduce the risks of operating with hydrogen as a carrier gas. Agilent GC software includes helpful tools, for example, the method translator. Method translation helps retain elution order when changing column dimensions, outlet pressure, speed of analysis, or carrier gas type. Using this tool to translate a single column method is relatively straight-forward, but with two columns in-series, the method translation requires some extra steps. Successful method translation for a multiple column configuration is best facilitated by working backwards, from the detector to the inlet. The method is first translated for the analytical column, and the resulting head pressure can then be used as the outlet pressure for the precolumn during its translation. Because the goal of this method translation was to maintain the same Figure 2. Method translation for the analytical column, an Agilent DB-WAXetr, from helium carrier gas to elution order and similar retention times, hydrogen carrier gas. 3 Table 1. Method parameters for both helium and hydrogen as carrier gas. ALS Oven Syringe Volume 5 µL 75 °C hold for 8 minutes Gradient 5 °C/min to 85 °C, hold 3 minutes Injection Volume 0.5 µL 40 °C/min to 140 °C, hold 0.4 minutes Wash Solvent Carbon disulfide Column 2 Detector (FID) Inlet (SSL) Heater 250 °C Mode Split Air 400 mL/min Heater On, 250 °C H2 40 mL/min (column + fuel = constant for H2 method) Split Ratio 100:1 Make-up N2 at 25 mL/min Septum Purge 3 mL/min Column 3 Detector (FID) Liner p/n 5190-6168 Heater 250 °C Columns Air 400 mL/min Agilent HP-1ms Ultra Inert, 30 m × 250 µm, 0.5 µm Column 1 H 40 mL/min (column + fuel = constant for H method) (p/n 19091S-633UI) 2 2 Make-up N at 25 mL/min Column 2 Agilent DB-WAXetr, 60 m × 320 µm, 1.0 µm (p/n 123-7364) 2 Column 3 Deactivated fused silica, 0.57 m × 100 µm CFT Device 2-way splitter with Pneumatic Switching Device Column Flow Helium Carrier (mL/min) Hydrogen Carrier (mL/min) Column 1 2 1.25 Column 2 2.7 1.96 Column 3 2.7 1.96 Toluene MIBK Benzene 9.6 10.0 10.4 10.8 11.2 11.6 12.0 12.4 12.8 13.2 13.6 14.0 14.4 Time (min) Figure 3. Overlaid chromatograms of the backflush timing standard running with helium carrier gas (blue) and hydrogen carrier gas (red). 4 Backflushing Performance criteria met the 95% confidence interval The initial backflush time was The performance was very similar for for the applicable concentration ranges determined from the monitor channel’s helium and hydrogen carrier gases of benzene and toluene for six injections signal. An injection of the backflush (Table 2). Benzene was well separated of calibration level 4, containing 0.67% timing and resolution mixture was from ethanol, greatly exceeding the benzene and 5.00% toluene by volume. made, and the time that the toluene resolution requirement of D3606. The The results for benzene and toluene from peak returned to baseline was recorded. calibration curve correlation coefficients locally sourced gasoline samples were This time was used as the starting point for benzene and toluene exceeded also determined to fall within the 95% for optimizing the backflush time. A 0.999 for both carrier gases. The S/N confidence interval specified in D3606 series of injections were made with the for benzene also greatly exceeded the across both carrier gas methods. backflush time consecutively reduced requirements of D3606. The repeatability by 0.02 minutes until the response of toluene began to decrease. The backflush timing from the injection Toluene With backflush just before the decrease in the toluene Without backflush response was used as the method backflush time. Figure 4 compares injections of a gasoline sample with and without backflush. Without backflush, several peaks can be seen to interfere with the peaks of interest. The peaks eluting after toluene are of no interest, Ethanol and backflushing them allows a much MIBK shorter run time.

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