Primary sludge hydrolysis for biological nutrient removal

被引:54
作者
Hatziconstantinou, GJ [1 ]
Yannakopoulos, P [1 ]
Andreadakis, A [1 ]
机构
[1] NATL TECH UNIV ATHENS,WATER RESOURCES DEPT,ATHENS 15780,GREECE
关键词
hydrolysis; primary sludge; fermenter; soluble carbon; nutrient removal;
D O I
10.1016/0273-1223(96)00545-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Primary sludge hydrolysis can enrich primary effluent with the soluble organics which in turn can be a valuable carbon source to subsequent nutrient removal processes. By controlling hydraulic retention time and temperature it is possible to confine the anaerobic digestion of the primary sludge to the acidogenic and acetogenic phase (hydrolysis/fermentation process), and take advantage of the soluble organics produced. This paper presents the results of a research involving bench and pilot scale experiments related to primary sludge hydrolysis. The pilot scale sedimentation tank (4.10 m in diameter, 3.20 m in depth) operated over an expended period of 21 months as a conventional clarifier and following this as a fermenter unit employing sludge recirculation. Parallel to the pilot scale experiments, several batch and continuous flow bench scale experiments were conducted in order to determine the factors controlling the production of soluble organics and the effect of the tatter on the denitrification process. The conclusions drawn were that a) a soluble COD production of the order of 5-6% in terms of sludge TCOD can be expected in a batch fermenter operating with HRT congruent to 2 days at T less than or equal to 20 degrees C, b) in a continuous flow fermenter, combinations of T > 20 degrees C and SRT > 2 should be applied in order to achieve a production of the order of 10%, c) significant soluble carbon production can be achieved in primary sedimentation tanks (over 30% in terms of influent SCOD) when relatively increased SRTs (4 to 5 days) in combination with sludge recirculation are employed, under T > 22 degrees C, and d) increased denitrification performance of the order of 9 mgNOx/g MLSS.hr, can be achieved with hydrolysate as a carbon source. Copyright (C) 1996 IAWQ.
引用
收藏
页码:417 / 423
页数:7
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