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Vaporization of JP-8 Jet Fuel in a Simulated Aircraft Fuel Tank ...

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5.1.2 Isooctane <strong>Fuel</strong> <strong>Vaporization</strong> Test<br />

Figure 5.5 shows results from s<strong>in</strong>gle component fuel vaporization at atmospheric pressure<br />

and reduced ambient temperature. Isooctane be<strong>in</strong>g quite volatile, it was necessary to<br />

allow the fuel to cool for several hours to near 3°F <strong>in</strong> order to obta<strong>in</strong> fuel vapor<br />

concentrations with<strong>in</strong> the FID calibration range <strong>of</strong> 0-4% propane equivalent. Figure 5.5<br />

shows that at the start <strong>of</strong> the test, after cool<strong>in</strong>g, there was very good agreement between<br />

the measured and calculated vapor concentration. As the fuel temperature <strong>in</strong>creased, the<br />

ullage vapor concentration also <strong>in</strong>creased due to <strong>in</strong>creas<strong>in</strong>g vaporization. The fuel vapor<br />

measurement was carried out <strong>in</strong>termittently at some times dur<strong>in</strong>g the test to preserve the<br />

purity <strong>of</strong> the sample, as the test time was almost 2 hours. Dur<strong>in</strong>g the latter part <strong>of</strong> the test<br />

the FID vapor concentration measurements fluctuated at high vapor concentrations above<br />

30,000 ppm. This was later seen <strong>in</strong> other experiments at high vapor concentrations as<br />

well, and was most likely due to some condensation occurr<strong>in</strong>g <strong>in</strong> the sample l<strong>in</strong>es at cold<br />

spots and subsequent vaporization at warmer locations. Consider<strong>in</strong>g the difficulties<br />

<strong>in</strong>volved <strong>in</strong> us<strong>in</strong>g isooctane as the test fuel, the agreement between the measured and<br />

calculated fuel vapor concentrations was considered satisfactory.<br />

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