Abiotic Nitrous Oxide (N2O) Production Is Strongly pH Dependent, but Contributes Little to Overall N2O Emissions in Biological Nitrogen Removal Systems

被引:69
作者
Su, Qingxian [1 ]
Domingo-Felez, Carlos [1 ]
Jensen, Marlene Mark [1 ]
Smets, Barth F. [1 ]
机构
[1] Tech Univ Denmark, Dept Environm Engn, DK-2800 Lyngby, Denmark
关键词
AMMONIA-OXIDIZING BACTERIA; NITRIFIER-DENITRIFICATION; DISSOLVED-OXYGEN; HYDROXYLAMINE; NITRITATION; WATER; ACID; MECHANISM; OXIDATION; KINETICS;
D O I
10.1021/acs.est.8b06193
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hydroxylamine (NH2OH) and nitrite (NO2-), intermediates during the nitritation process, can engage in chemical (abiotic) reactions that lead to nitrous oxide (N2O) generation. Here, we quantify the kinetics and stoichiometry of the relevant abiotic reactions in a series of batch tests under different and relevant conditions, including pH, absence/presence of oxygen, and reactant concentrations. The highest N2O production rates were measured from NH2OH reaction with HNO2, followed by HNO2 reduction by Fe2+, NH2OH oxidation by Fe3+, and finally NH2OH disproportionation plus oxidation by O-2. Compared to other examined factors, pH had the strongest effect on N2O formation rates. Acidic pH enhanced N2O production from the reaction of NH2OH with HNO2 indicating that HNO2 instead of N2O- was the reactant. In departure from previous studies, we estimate that abiotic N2O production contributes little (< 3% of total N2O production) to total N2O emissions in typical nitritation reactor systems between pH 6.5 and 8. Abiotic contributions would only become important at acidic pH 5). In consideration of pH effects on both abiotic and biotic N2O production pathways, circumneutral pH set-points are suggested to minimize overall N2O emissions from nitritation systems.
引用
收藏
页码:3508 / 3516
页数:9
相关论文
共 48 条
[1]   Metal-catalyzed anaerobic disproportionation of hydroxylamine.: Role of diazene and nitroxyl intermediates in the formation of N2, N2O, NO+, and NH3 [J].
Alluisetti, GE ;
Almaraz, AE ;
Amorebieta, VT ;
Doctorovich, F ;
Olabe, JA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (41) :13432-13442
[2]   COPPER-CATALYSED OXIDATION OF HYDROXYLAMINE [J].
ANDERSON, JH .
ANALYST, 1964, 89 (105) :357-&
[3]   OXIDATION OF HYDROXYLAMINE BY NITROUS AND NITRIC-ACIDS [J].
BENNETT, MR ;
BROWN, GM ;
MAYA, L ;
POSEY, FA .
INORGANIC CHEMISTRY, 1982, 21 (06) :2461-2468
[4]  
Bonner F. T., 1988, Comments Inorg. Chem., V7, P215
[5]   THE REACTION OF NITROUS ACID WITH HYDROXYLAMINE [J].
BOTHNERBY, A ;
FRIEDMAN, L .
JOURNAL OF CHEMICAL PHYSICS, 1952, 20 (03) :459-462
[6]   FORMATION OF NITROUS-OXIDE AND DINITROGEN BY CHEMICAL DECOMPOSITION OF HYDROXYLAMINE IN SOILS [J].
BREMNER, JM ;
BLACKMER, AM ;
WARING, SA .
SOIL BIOLOGY & BIOCHEMISTRY, 1980, 12 (03) :263-269
[7]   RATES OF NITROUS-OXIDE PRODUCTION IN THE OXIDATION OF HYDROXYLAMINE BY IRON(III) [J].
BUTLER, JH ;
GORDON, LI .
INORGANIC CHEMISTRY, 1986, 25 (25) :4573-4577
[8]  
deGraaf AAV, 1996, MICROBIOL-UK, V142, P2187
[9]   Floc-based sequential partial nitritation and anammox at full scale with contrasting N2O emissions [J].
Desloover, Joachim ;
De Clippeleir, Haydee ;
Boeckx, Pascal ;
Du Laing, Gijs ;
Colsen, Joop ;
Verstraete, Willy ;
Vlaeminck, Siegfried E. .
WATER RESEARCH, 2011, 45 (09) :2811-2821
[10]   Calibration of the comprehensive NDHA-N2O dynamics model for nitrifier-enriched biomass using targeted respirometric assays [J].
Domingo-Felez, Carlos ;
Caldero-Pascual, Maria ;
Sin, Gurkan ;
Plosz, Benedek G. ;
Smets, Barth F. .
WATER RESEARCH, 2017, 126 :29-39