用户名: 密码: 验证码:
A~2/O耦合生物曝气滤池强化污水脱氮除磷
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:RESEARCH ON ENHANCED NITROGEN AND PHOSPHORUS REMOVAL FROM WASTEWATER BY A~2/O COUPLED BIOLOGICAL AERATED FILTER
  • 作者:殷芳芳 ; 胡恩保
  • 英文作者:YIN Fang-fang;HU En-bao;Zhejiang Tongji Vocational College of Science and Technology;
  • 关键词:A~2/O ; BAF ; 生物脱氮除磷 ; 温度
  • 英文关键词:A2/O;;BAF;;biological nitrogen and phosphorus removal;;temperature
  • 中文刊名:HJGC
  • 英文刊名:Environmental Engineering
  • 机构:浙江同济科技职业学院;
  • 出版日期:2019-06-15
  • 出版单位:环境工程
  • 年:2019
  • 期:v.37;No.252
  • 基金:浙江省水利厅课题(RC1624);; 浙江省2016年度高等教育教学改革项目(Jg20160407)
  • 语种:中文;
  • 页:HJGC201906015
  • 页数:5
  • CN:06
  • ISSN:11-2097/X
  • 分类号:76-80
摘要
为了强化污水脱氮除磷性能,采用厌氧/缺氧/好氧(A~2/O)耦合生物曝气滤池(BAF)组合工艺,考察其对营养盐和有机物去除效果,并进一步探究温度的潜在影响。结果表明:A~2/O耦合BAF能实现有机物和氮、磷的同步深度去除,有机物、TN和TP去除率分别高达90%、85. 2%和93%。温度为15,25,35℃时COD去除率变化不大,基本维持在90%以上,45℃时略低于其他温度。NH_4~+-N去除率随温度的升高呈现上升趋势,NO_2~--N、NO_3~--N去除效果在35℃时最佳,厌氧释磷量和缺氧、好氧吸磷量也在35℃达到最大值。可见,A~2/O耦合BAF系统最佳脱氮除磷温度为35℃。
        In order to strengthen the performance of nitrogen and phosphorus removal from wastewater,the combination of anaerobic/anoxic/aerobic( A~2/O) coupled biological aeration filter( BAF) was used to investigate the removal of nutrients and organic matters,and the potential effect of temperature was further researched. The results showed that: A~2/O coupled with BAF could realize the simultaneous deep removed of organic matters,nitrogen and phosphorus,and the removal rates of organic matters,total nitrogen and total phosphorus were as high as 90%,85. 2% and 93%,respectively. The COD removal rate did not change much at 15 ℃,25 ℃ and 35 ℃,remained substantially above 90%,and at 45 ℃ it was slightly lower than that at other temperature conditions. The removal efficiency of NH_4~+-N increased with the increase of temperature. At 35 ℃,NO_2~--N and NO_3~--N had the best removal effect,and the anaerobic phosphorus release and anoxia and aerobic phosphorus absorption were also at the maximum values. Thus,35 ℃ was the optimal denitrification temperature and phosphorus removal temperature in A~2/O coupled BAF system.
引文
[1] Rahimi Y, Torabian A, Mehrdadi N, et al. Simultaneous nitrification-denitrification and phosphorus removal in a fixed bed sequencing batch reactor(FBSBR)[J]. Journal of Hazardous Materials,2011,185(2/3):852-857.
    [2] Rao Y S, Tyagi R D, Scheible O K, et al. Nitrification,denitrification and phosphorus removal in sequential batch reactors[J]. Bioresource Technology,1997,61(2):151-157.
    [3]李亚静,孙力平.常规A2/O工艺和倒置A2/O工艺处理城市污水比较研究[J].环境工程,2015,33(增刊1):967-970.
    [4]马军,邱立平.曝气生物滤池及其研究进展[J].环境工程,2002,20(3):7-11.
    [5]朱加乐,林燕,王欣泽,等.曝气生物滤池脱氮的研究进展[J].化工进展,2017,36(3):1077-1083.
    [6]马娟,彭永臻,王丽,等.温度对反硝化过程的影响以及pH值变化规律[J].中国环境科学,2008,28(11):1004-1008.
    [7] Kuba T,Loosdrecht M C M V,Heijnen J J. Phosphorus and nitrogen removal with minimal COD requirement by integration of denitrifying dephosphatation and nitrification in a two-sludge system[J]. Water Research,1996,30(7):1702-1710.
    [8]国家环境保护总局《水和废水监测分析方法》编委会.水和废水监测分析方法[M].4版.北京:中国环境科学出版社,2002.
    [9] Sayi-Ucar N,Sarioglu M,Insel G,et al. Long-term study on the impact of temperature on enhanced biological phosphorus and nitrogen removal in membrane bioreactor[J]. Water Research,2015,84:8-17.
    [10] Wei X C,Viadero J R,Bhojappa S. Phosphorus removal by acid mine drainage sludge from secondary effluents of municipal wastewater treatment plants[J]. Water Research,2008,42(13):3275-3284.
    [11] Hao X D,Heijnen J J,Van Loosdrecht M C. Model-based evaluation of temperature and inflow variations on a partial nitrification-ANAMMOX biofilm process[J]. Water Research,2002,36(19):4839-4849.
    [12] Kim J H,Guo X J,Park H S. Comparison study of the effects of temperature and free ammonia concentration on nitrification and nitrite accumulation[J]. Process Biochemistry,2008,43(2):154-160.
    [13]张玲,彭党聪,常蝶.温度对聚磷菌活性及基质竞争的影响[J].环境科学,2017,38(6):2429-2434.
    [14]王亚宜,王淑莹,彭永臻,等.污水有机碳源特征及温度对反硝化聚磷的影响[J].环境科学学报,2006,26(2):186-192.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700