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N2O production in a single stage nitritation/anammox MBBR process

N2O production in a single stage nitritation/anammox MBBR process

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laboratory system might be underestimated. If calibrations have been performed with<br />

an unsaturated <strong>N2O</strong> solution this will give rise to overestimated <strong>N2O</strong> <strong>production</strong>s from<br />

the partial <strong>nitritation</strong>/<strong>anammox</strong> <strong>MBBR</strong>. As po<strong>in</strong>ted out by Kampschreur et al., (2009)<br />

chang<strong>in</strong>g environmental conditions might lead to higher <strong>N2O</strong> emissions and short term<br />

laboratory scale measurements might therefore give over estimated <strong>N2O</strong> emissions.<br />

S<strong>in</strong>ce the <strong>anammox</strong> <strong>process</strong> needs less resources and produces less CO2 than common<br />

nitrogen removal, <strong>anammox</strong> has been po<strong>in</strong>ted out as a more environmental friendly<br />

alternative (Fux and Siegrist, 2004). Kuenen and Robertson, (1994) are call<strong>in</strong>g attention<br />

to that wastewaters <strong>in</strong> the Netherlands generally have a nitrogen content between 40-60<br />

mg/l, each person produces about 150 l/d which gives a nitrogen <strong>production</strong> of 2.2 kg<br />

nitrogen per person and year and that even a small <strong>N2O</strong> <strong>production</strong> correspond<strong>in</strong>g to<br />

0.1% of the nitrogen concentration will result <strong>in</strong> significant <strong>N2O</strong> emissions. Consider<strong>in</strong>g<br />

that the <strong>MBBR</strong> <strong>process</strong> has been found to produce <strong>N2O</strong> correspond<strong>in</strong>g to a m<strong>in</strong>imum of<br />

2% of removed <strong>in</strong>organic nitrogen it has to be further exam<strong>in</strong>ed whether this s<strong>in</strong>gle<br />

<strong>stage</strong> <strong>anammox</strong> <strong>process</strong> is more environmental friendly than common nitrogen removal<br />

<strong>process</strong>es. Even if rather high <strong>N2O</strong> <strong>production</strong> was obta<strong>in</strong>ed <strong>in</strong> this study, experiences <strong>in</strong><br />

pilot scale trials with similar operation modes has given <strong>N2O</strong> <strong>production</strong> as low as 0.2 %<br />

of removed <strong>in</strong>organic nitrogen (Christensson, 2010). Additional research is needed to<br />

determ<strong>in</strong>e if the <strong>N2O</strong> <strong>production</strong> from a full scale <strong>process</strong> would be as high as the<br />

<strong>production</strong> found from the laboratory <strong>MBBR</strong> system. It also has to be determ<strong>in</strong>ed which<br />

bacteria that are responsible for produc<strong>in</strong>g <strong>N2O</strong>, whether the relatively high <strong>N2O</strong><br />

emissions found from the laboratory <strong>MBBR</strong> are due to biofilm structure with oxygen<br />

pore conditions. Amounts of <strong>N2O</strong> emissions have to be further evaluated <strong>in</strong> correlation<br />

to <strong>process</strong> operation and performance. A s<strong>in</strong>gle <strong>stage</strong> biofilm system might not be the<br />

best solution for the partial <strong>nitritation</strong> <strong>anammox</strong> <strong>process</strong> if this <strong>process</strong> design always<br />

gives rise to high <strong>N2O</strong> emissions.<br />

5.3 Measurements with NO2-N biosensor<br />

The biosensor gave results that correlated very well with concentrations obta<strong>in</strong>ed with<br />

LCK 342 at some occasions and the fluctuations <strong>in</strong> NO2-N concentration measured with<br />

the biosensor always showed the same trends as achieved with LCK 342. However the<br />

NO2-N biosensor did not give reliable results at all times <strong>in</strong> use and could never replace<br />

LCK 342 for determ<strong>in</strong>ation of NO2-N concentrations dur<strong>in</strong>g this master thesis work.<br />

Some measurements performed with the biosensor recorded much higher NO2-N<br />

concentrations than obta<strong>in</strong>ed with the Dr. Lange kit. This was probably due to electric<br />

disturbances that caused electric migration which is the transport of a charged body <strong>in</strong><br />

an electric field. Kjær et al., (1999), have shown that this phenomenon can be used to<br />

force negatively charged NO3 − ions over the semi permeable membrane of the<br />

biochamber <strong>in</strong>creas<strong>in</strong>g the ion sensitivity by a factor of more than 10.000. The electric<br />

disturbances can have been caused by other laboratory equipment or s<strong>in</strong>ce the ground<br />

channel on the backside of the piccoameter was used. This ground port has another<br />

47

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