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Experimental Study of Biodegradation of Ethanol and Toluene Vapors

Experimental Study of Biodegradation of Ethanol and Toluene Vapors

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3.4 <strong>Experimental</strong> Procedures<br />

Figure 3-1 is a schematic <strong>of</strong> the experimental apparatus used throughout this<br />

investigation. Air stripping <strong>and</strong> bioremediation experiments were all performed at 25<br />

ºC in a 3 L, baffled New Brunswick Scientific Bi<strong>of</strong>low III well-mixed bioreactor at a<br />

working volume <strong>of</strong> 1.5 L. One six-blade Rushton impeller was positioned 3.5 cm from<br />

the bottom <strong>of</strong> the vessel. For biodegradation investigations, air was normally supplied<br />

through two, metered inlet streams. All air flowmeters were calibrated using a Wet Test<br />

flowmeter <strong>and</strong> the calibration curves are given in Appendix B (See Figure B-8). In<br />

order to obtain the desired gas inlet concentration <strong>of</strong> ethanol or toluene, one air stream<br />

passed through a bubbler filled with either ethanol or toluene which was maintained in a<br />

water bath at 21.0 ± 0.5 ºC; the other stream by-passed the bubbler. These two air<br />

streams were then mixed downstream <strong>of</strong> the bubbler <strong>and</strong> directly entered the bioreactor.<br />

In this way, the concentration <strong>of</strong> ethanol or toluene entering the bioreactor could be<br />

precisely controlled. In some runs, a third stream was employed which passed through<br />

a second bubbler. Thus, ethanol <strong>and</strong> toluene could be simultaneously added to the<br />

bioreactor. For continuous runs, fresh sterile nutrient media was pumped into the<br />

bioreactor <strong>and</strong> spent fermentation broth was removed at identical flowrates.<br />

3.4.1 Mass Transfer<br />

Mass transfer studies <strong>of</strong> toluene <strong>and</strong> ethanol from contaminated air streams to<br />

the liquid phase, along with oxygen mass transfer studies, were carried out using a<br />

st<strong>and</strong>ard stirred tank bioreactor (model GF0014, Chemap AG, Switzerl<strong>and</strong>). The liquid<br />

volume used was 12 liters <strong>and</strong> the operating temperature was maintained at 25 ± 0.5 o C<br />

for all runs. The general specifications <strong>of</strong> the reactor are presented in Table C-1. The<br />

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