N2O production in a single stage nitritation/anammox MBBR process
N2O production in a single stage nitritation/anammox MBBR process
N2O production in a single stage nitritation/anammox MBBR process
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m<strong>in</strong>imum concentration of 2 mg/l should be ma<strong>in</strong>ta<strong>in</strong>ed (Gray, 2004). The nitrify<strong>in</strong>g rate<br />
<strong>in</strong>creases up to DO levels of 3-4 mg/l, (Metcalf & Eddy). All figures given here yields for<br />
DO concentrations <strong>in</strong> the water bulk phase of activated sludge <strong>process</strong>es, higher DO<br />
concentrations are needed to satisfy the microbial oxygen demand <strong>in</strong> biofilm <strong>process</strong>es.<br />
This s<strong>in</strong>ce the oxygen concentration <strong>in</strong> the biofilm depends on diffusion of oxygen from<br />
the water phase <strong>in</strong>to the biofilm which is further expla<strong>in</strong>ed <strong>in</strong> chapter 2.4.<br />
Both denitrification and <strong>anammox</strong> <strong>process</strong>es are <strong>in</strong>hibited by oxygen. Denitrification has<br />
been observed to be <strong>in</strong>hibited at DO concentrations above 0.2 mg/l (Metcalf & Eddy,<br />
2003) and <strong>anammox</strong> organisms are reversibly <strong>in</strong>hibited by DO concentrations as low as<br />
2 µmole/l or 0.032 mg/l, (Jetten et al., 1998).<br />
2.2.2 Temperature<br />
The temperature impacts the structure of the microbial community and is crucial for<br />
growth and reaction rates <strong>in</strong> the system. Microbial reactions are often dependent on<br />
enzyme-catalysed reactions that <strong>in</strong>crease <strong>in</strong> velocity at higher temperatures. When the<br />
time for a reaction to be catalysed is shortened the metabolism is more active and the<br />
microorganism is allowed to grow faster (Prescott et al., 2005). Temperature does also<br />
impact non viable factors like settl<strong>in</strong>g characteristics, gas solubility and transfer rates<br />
(Gray, 2004).<br />
Nitrification can be operated <strong>in</strong> a temperature <strong>in</strong>terval of 0-40 °C with a temperature<br />
optimum between 30-35 °C (Gray, 2004). Denitrify<strong>in</strong>g bacteria are less sensitive to<br />
temperature than nitrifiers and denitrification can take place <strong>in</strong> a temperature <strong>in</strong>terval<br />
from 2-75 °C with an optimum around 30 °C (Pierzynski et al., 2005)<br />
Anammox bacteria are active <strong>in</strong> temperature range from 6-43 °C with an optimum at 30<br />
̊C (Anammox onl<strong>in</strong>e).<br />
2.2.3 pH and alkal<strong>in</strong>ity<br />
pH, which is the measurement of a solutions acidity or alkal<strong>in</strong>ity, is another important<br />
environmental factor that impacts the growth rate of the microbial community. S<strong>in</strong>ce pH<br />
is def<strong>in</strong>ed as the <strong>in</strong>verse logarithm of H + ions <strong>in</strong> solution a change of one pH unit<br />
corresponds to a tenfold <strong>in</strong>crease <strong>in</strong> the activity of H + ions. Each bacteria species have a<br />
pH growth range and optimum.<br />
Nitrification consumes alkal<strong>in</strong>ity s<strong>in</strong>ce two moles of OH − are used per mole ammonium<br />
oxidised. Nitrification is favoured by mild alkal<strong>in</strong>e conditions with pH optimum <strong>in</strong> the<br />
range of pH 8.0-8.4 (Gray, 2004). The nitrification rate is significantly decl<strong>in</strong>ed by low<br />
pH values