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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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The microsensor is connected to a piccoameter that polarises the cathode surface where<br />

the nitrous oxide that diffuses through the silicone membrane is reduced to N2 gas. As<br />

nitrous oxide is reduced at the cathode surface two electrons from the silver anode is<br />

used for each reduced <strong>N2O</strong> molecule. The electron transport gives rise to a current<br />

proportional to the amount of reduced nitrous oxide. The current is registered and<br />

converted to an out signal by the piccoameter. The guard cathode is also polarised to<br />

deplete oxygen <strong>in</strong> the electrolyte which m<strong>in</strong>imizes zero current (Unisense b, 2007).<br />

The nitrous oxide sensor has a measur<strong>in</strong>g range of about 0-1 atmosphere p<strong>N2O</strong> with a<br />

response time less than 10 seconds. The stirr<strong>in</strong>g sensitivity is smaller than 2% and the<br />

out signal is temperature dependent with a temperature coefficient of about 2-3% per<br />

°C. Interference <strong>in</strong> the out signal might occur from electrical noise <strong>in</strong> the surround<strong>in</strong>g<br />

environment (Unisense b, 2007).<br />

2.6.2 Nitrite biosensor<br />

The nitrite biosensor is a nitrous oxide sensor equipped with a replaceable biochamber<br />

(Figure 9a), (Unisense e, 2009). A plastic tube conta<strong>in</strong><strong>in</strong>g a carbon source and a bacterial<br />

culture constitutes the biochamber that is mounted <strong>in</strong> the front of the sensor tip (Figure<br />

9b), (Unisense e, 2009). The biomass <strong>in</strong> the reaction chamber is positioned between the<br />

carbon source required for their growth and an ion-permeable membrane separat<strong>in</strong>g<br />

the microorganisms from the external environment (Unisense c, 2007).<br />

The denitrify<strong>in</strong>g bacterial culture used <strong>in</strong> the biochamber is deficient <strong>in</strong> NO3 − and <strong>N2O</strong><br />

reductase which means that it is only able to reduce NO2 − <strong>in</strong>to <strong>N2O</strong>. As NO2 − diffuses <strong>in</strong>to<br />

the biochamber it is reduced to <strong>N2O</strong> by the biomass (Nielsen et al., 2004). S<strong>in</strong>ce<br />

denitrify<strong>in</strong>g bacteria are facultative aerobic they can use both oxygen and nitrite as<br />

oxidation agent for their respiration (Larsen et al., 1997). Oxygen is used preferential to<br />

nitrite as it results <strong>in</strong> a higher energy yield. This will create a NO2 − reduc<strong>in</strong>g gradient <strong>in</strong><br />

the biochamber with the bacteria closest to the membrane respir<strong>in</strong>g with oxygen. The<br />

NO2 − reduc<strong>in</strong>g capacity of the biosensor will depend on the length of the aerobic zone<br />

result<strong>in</strong>g <strong>in</strong> higher maximum detectable concentrations of NO2 − <strong>in</strong> anaerobic<br />

environments (Larsen et al., 1997).<br />

Produced <strong>N2O</strong> diffuses through the silicone membrane and is reduced at the cathode <strong>in</strong><br />

the transducer part of the biosensor. A piccoameter measures the current aris<strong>in</strong>g from<br />

the electron transport just as <strong>in</strong> the case with the nitrous oxide sensor. The output signal<br />

is proportional to the amount of NO2 − that has been reduced after diffusion <strong>in</strong>to the<br />

biochamber (Unisense c, 2007).<br />

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