Comparison of inhibitory roles on nitrite-oxidizing bacteria by hydroxylamine and hydrazine during the establishment
Junkai Zhao1, Shuhan Lei2, Guangwei Cheng3
1School of Water and Environment, Chang'an University, Xi'an 710064, Shaanxi, China; Key Laboratory of Subsurface Hydrology and Ecological Effect in Arid Region (Chang'an University), Ministry of Education, Xi'an 710064, Shaanxi, China.
Abstract:
The inhibitory roles of hydroxylamine (NH2OH) and hydrazine (N2H4) on nitrite-oxidizing bacteria were investigated in a comparative study. The results showed that nitrite accumulation was achieved by adding 5 mg-N/L NH2OH or N2H4 to two parallel sequencing batch reactors, with nitrite accumulation rate reaching 95.83% and 86.58% within 15 days after adopting aeration time control, respectively. Correspondingly, the maximum level of NO in typical cycles caused by NH2OH addition was 0.18 mg-N/L, which was higher than obtained for N2H4. NH2OH or N2H4 showed strong inhibition on Nitrospira and promoted the enrichment of Nitrosomonas, with the effects of NH2OH being more significant. However, nitritation began to deteriorate after the cessation of inhibitors addition. In conclusion, NH2OH was a better inhibitor than N2H4 for Nitrospira. The inhibitory role of NH2OH was primarily related to NO toxicity, while for N2H4 it was attributed to its own toxicity, with NO playing a smaller role.
More Related Videos
Related Concept Videos
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
2° Amines to N-Nitrosamines: Reaction with NaNO2
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Diazonium Group Substitution: –OH and –H
Inorganic Nitrogen Assimilation


