Simultaneous urea hydrolysis, formaldehyde removal and denitrification in a multifed upflow filter under anoxic and anaerobic conditions

被引:48
作者
Garrido, JM [1 ]
Méndez, R [1 ]
Lema, JM [1 ]
机构
[1] Univ Santiago de Compostela, Inst Technol, Dept Chem Engn, Santiago De Compostela 15706, Spain
关键词
multifed upflow filter; denitrification; formaldehyde; nitrous oxide; urea hydrolysis;
D O I
10.1016/S0043-1354(00)00311-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A multifed upflow filter (MUF), working under anoxic or anaerobic conditions, coupled with an aerobic biofilm airlift suspension (BAS) reactor was operated in order to treat a wastewater with high formaldehyde (up to 1.5 g L-1) and urea (up to 0.46 g L-1) concentrations. In the MUF, formaldehyde removal, denitrification and urea hydrolysis took place simultaneously. The MUF was operated at 37 degreesC, at a hydraulic retention time (HRT) ranging from 1 to 0.3 d. An organic loading rate (OLR) of 0.5 kg-formaldehyde m(-3) d(-1) was efficiently eliminated during anaerobic operation and transformed into methane, while a much higher OLR (up to 2 kg-formaldehyde m(-3) d(-1)) was oxidised under anoxic conditions by the nitrite or nitrate From the nitrifying airlift. However, only 80% of urea was hydrolysed to ammonia in an anoxic environment while complete conversion occurred under anaerobic conditions. Moreover, formaldehyde concentrations higher than 50 mg L-1 provoked a loss of efficiency of urea hydrolysis, decreasing to 10% at formaldehyde concentrations above 300 mg L-1 Methane production rate during the anaerobic stage was adversely affected by accumulations of formaldehyde in the reactor causing lower formaldehyde removal efficiency. However, denitrification proceeded properly even at a formaldehyde concentration of 700 mg L-1 in the reactor, although nitrous oxide appears in the off-gas. The COD/N ratios required For complete nitrite and nitrate denitrification with formaldehyde were estimated at 2.1 and 3.5 kg-COD/kg-N, respectively. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:691 / 698
页数:8
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