CN102515352A - Method for removing ammonia nitrogen from industrial waste water produced in synthetic ammonia industry - Google Patents
Method for removing ammonia nitrogen from industrial waste water produced in synthetic ammonia industry Download PDFInfo
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 title claims abstract description 64
- 229910021529 ammonia Inorganic materials 0.000 title claims abstract description 30
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 title claims abstract description 30
- 238000000034 method Methods 0.000 title claims abstract description 23
- 239000010842 industrial wastewater Substances 0.000 title abstract description 17
- 239000001301 oxygen Substances 0.000 claims abstract description 26
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 25
- 238000006243 chemical reaction Methods 0.000 claims abstract description 15
- 239000010865 sewage Substances 0.000 claims abstract description 13
- 239000002351 wastewater Substances 0.000 claims description 44
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 238000010992 reflux Methods 0.000 claims description 13
- JVMRPSJZNHXORP-UHFFFAOYSA-N ON=O.ON=O.ON=O.N Chemical compound ON=O.ON=O.ON=O.N JVMRPSJZNHXORP-UHFFFAOYSA-N 0.000 claims description 12
- 239000010802 sludge Substances 0.000 claims description 6
- 238000007034 nitrosation reaction Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000011259 mixed solution Substances 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims 10
- 238000006396 nitration reaction Methods 0.000 claims 5
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 abstract description 8
- 238000004062 sedimentation Methods 0.000 abstract description 7
- 230000003647 oxidation Effects 0.000 abstract description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052799 carbon Inorganic materials 0.000 abstract description 4
- 239000003513 alkali Substances 0.000 abstract description 3
- 238000005265 energy consumption Methods 0.000 abstract description 3
- 230000014759 maintenance of location Effects 0.000 description 14
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 8
- 241000894006 Bacteria Species 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 3
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 238000002306 biochemical method Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001546 nitrifying effect Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
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Abstract
本发明公开了一种合成氨工业废水中氨氮脱除方法,合成氨工业废水依次进入缺氧池、厌氧池、微氧池、好氧池和沉淀池,微氧池中一部分污水回流到厌氧池,好氧池中一部分污水回流到缺氧池,沉淀池中的一部分污水回流到缺氧池的进水端。本发明将缺氧反硝化、厌氧氨氧化、短程硝化反硝化在同一生物处理系统中实现。实现短程硝化反硝化,节省25%的供氧量和40%的有机碳源,缩短反应停留时间,减少容积;实现厌氧氨氧化,降低能耗,防止二次污染;氨氮去除率高,达到99%以上;整个过程碱的消耗量减少,运行费用低。The invention discloses a method for removing ammonia nitrogen from synthetic ammonia industrial wastewater. The synthetic ammonia industrial wastewater enters anoxic pool, anaerobic pool, microoxic pool, aerobic pool and sedimentation pool in turn, and part of the sewage in the microoxic pool flows back into the anaerobic pool. , part of the sewage in the aerobic tank is returned to the anoxic tank, and part of the sewage in the sedimentation tank is returned to the inlet of the anoxic tank. The invention realizes anoxic denitrification, anaerobic ammonium oxidation and short-range nitrification and denitrification in the same biological treatment system. Realize short-range nitrification and denitrification, save 25% of oxygen supply and 40% of organic carbon source, shorten reaction residence time, reduce volume; realize anaerobic ammonium oxidation, reduce energy consumption, and prevent secondary pollution; high ammonia nitrogen removal rate, reaching More than 99%; the consumption of alkali in the whole process is reduced, and the operating cost is low.
Description
技术领域 technical field
本发明涉及一种废水中氨氮的脱除方法,特别是合成氨工业废水中氨氮的脱除方法。 The invention relates to a method for removing ammonia nitrogen in waste water, in particular to a method for removing ammonia nitrogen in synthetic ammonia industrial waste water.
背景技术 Background technique
合成氨工业在生产过程中产生大量含氨氮工业废水,该行业废水具有污染物种类多、可生化性差、碳氮比值低、氨氮含量高等特点。目前,合成氨工业废水普通采用生化方法进行处理,特别是采用以A/O脱氮为代表的生物脱氮工艺。该工艺原理是废水中的氨氮,在好氧的条件下被硝化菌硝化为硝态氮,大量硝态氮回流至缺氧段,在缺氧条件下,通过兼性厌氧反硝化菌作用,以废水中有机物作为电子供体,硝态氮作为电子受体,使硝态氮被还原为氮气,逸入大气从而达到最终脱氮的目的。该工艺中好氧段需要的鼓风空气量大,动力消耗大,而且需要补充的碱量大;缺氧段需要补充大量有机碳源,在合成氨工业废水碳氮比值低的条件下,反硝化速率低,补充有机碳源量大,操作费用高;该工艺脱氮效率低,为了提高脱氮率,必须提高回流比,但高的回流比造成缺氧段富氧化,破坏反硝化环境,降低了反硝化率,同时增加了动能消耗。 The synthetic ammonia industry produces a large amount of ammonia-nitrogen-containing industrial wastewater during the production process. The wastewater in this industry has the characteristics of many types of pollutants, poor biodegradability, low carbon-nitrogen ratio, and high ammonia-nitrogen content. At present, the synthetic ammonia industrial wastewater is generally treated by biochemical methods, especially the biological denitrification process represented by A/O denitrification. The principle of this process is that the ammonia nitrogen in the wastewater is nitrified into nitrate nitrogen by nitrifying bacteria under aerobic conditions, and a large amount of nitrate nitrogen flows back to the anoxic section. Under anoxic conditions, through the action of facultative anaerobic denitrifying bacteria, The organic matter in the wastewater is used as the electron donor, and the nitrate nitrogen is used as the electron acceptor, so that the nitrate nitrogen is reduced to nitrogen gas, which escapes into the atmosphere to achieve the purpose of final denitrification. In the process, the aerobic section requires a large amount of blast air, large power consumption, and a large amount of alkali to be supplemented; the anoxic section needs to supplement a large amount of organic carbon sources. Under the condition of low carbon-nitrogen ratio of ammonia industrial wastewater, denitrification The rate is low, the amount of supplementary organic carbon source is large, and the operating cost is high; the denitrification efficiency of this process is low. In order to improve the denitrification rate, the reflux ratio must be increased, but the high reflux ratio will cause rich oxidation in the anoxic section, destroy the denitrification environment, and reduce The denitrification rate is improved, and the kinetic energy consumption is increased at the same time.
发明内容 Contents of the invention
本发明的目的是提供一种处理效率高,运行费用低、投资小的合成氨工业废水中氨氮脱除方法,它可使该行业废水排放达到国家标准。 The purpose of the present invention is to provide a method for removing ammonia nitrogen in synthetic ammonia industrial wastewater with high treatment efficiency, low operating cost and small investment, which can make the wastewater discharge of this industry reach the national standard.
本发明技术方案包括以下内容:一种合成氨工业废水中氨氮脱除方法,合成氨工业废水依次进入缺氧池、厌氧池、微氧池、好氧池和沉淀池,微氧池中一部分污水回流到厌氧池,好氧池中一部分污水回流到缺氧池,沉淀池中的一部分污水回流到缺氧池的进水端。 The technical scheme of the present invention includes the following contents: a method for removing ammonia nitrogen in synthetic ammonia industrial wastewater, wherein the synthetic ammonia industrial wastewater enters the anoxic pool, the anaerobic pool, the microoxic pool, the aerobic pool and the sedimentation pool in turn, and a part of the sewage in the microoxic pool flows back To the anaerobic tank, part of the sewage in the aerobic tank is returned to the anoxic tank, and part of the sewage in the sedimentation tank is returned to the inlet end of the anoxic tank.
所述合成氨工业废水先进入缺氧池中,与含有硝态氮(NO3 --N)的回流混合液混合进行脱氮反应,以废水中有机物作为电子供体,以硝态氮(NO3 --N)作为电子受体,NO3 --N被还原为氮气(N2)脱除;缺氧池中脱氮之后的废水进入厌氧池中,在厌氧池中与含有亚硝态氮(NO2 --N)的回流水混合进行厌氧氨氧化反应,以废水中的氨氮(NH4 +-N)做电子供体,以亚硝态氮(NO2 --N)为电子受体,将NH4 +-N或NO2 --N转变成N2;厌氧池中含有NH4 +-N的废水进入微氧池中,进行亚硝化反应,把NH4 +-N氧化为NO2 --N,同时微氧池中含有NO2 --N的污水一部分回流到厌氧池;微氧池剩余的含有NO2 --N的废水进入好氧池中,进行硝化反应,NO2 --N被氧化形成NO3 --N,好氧池中含有NO3 --N的废水一部分通过回流到缺氧池进行反硝化脱氮,好氧池中剩余的含有NO3 --N的废水经沉淀池泥水分离后达标排放,沉淀污泥回流到缺氧池。 The synthetic ammonia industrial wastewater first enters the anoxic pool, and is mixed with the reflux mixture containing nitrate nitrogen (NO 3 - -N) for denitrification reaction. The organic matters in the wastewater are used as electron donors, and the nitrate nitrogen (NO 3 - -N) As an electron acceptor, NO 3 - -N is reduced to nitrogen (N 2 ) and removed; the wastewater after denitrification in the anoxic pool enters the anaerobic pool, and in the anaerobic pool, it contains nitrite The reflux water of nitrogen (NO 2 - -N) is mixed for anaerobic ammonium oxidation reaction, the ammonia nitrogen (NH 4 + -N) in the wastewater is used as the electron donor, and the nitrite nitrogen (NO 2 - -N) is used as the electron donor Acceptor, convert NH 4 + -N or NO 2 - -N into N 2 ; the wastewater containing NH 4 + -N in the anaerobic tank enters the micro-aerobic tank for nitrosation reaction, and oxidizes NH 4 + -N At the same time, part of the sewage containing NO 2 - -N in the micro-aerobic pool is returned to the anaerobic pool; the remaining waste water containing NO 2 - -N in the micro-aerobic pool enters the aerobic pool for nitrification. NO 2 - -N is oxidized to form NO 3 - -N, part of the wastewater containing NO 3 - -N in the aerobic tank is returned to the anoxic tank for denitrification and denitrification, and the rest in the aerobic tank contains NO 3 - - The waste water of N is separated from the mud and water in the sedimentation tank and discharged up to the standard, and the sedimented sludge is returned to the anoxic tank.
在缺氧池中的反硝化反应是在PH=7.5-9.2,溶解氧(DO)小于0.5mg/L条件下进行;在厌氧池中的反硝化反应是在PH=7.0-8.5,溶解氧(DO)小于0.2mg/L条件下进行;在微氧池中的反硝化反应是在PH=7.4-8.3,溶解氧(DO)在0.5-1.0mg/L条件下进行;在好氧池中的反硝化反应是在PH=6.5-8.0,溶解氧(DO)在2.0-4.0mg/L条件下进行;混合液回流比为100-300%;缺氧池中水力停留时间是7-14小时;厌氧池中水力停留时间是9-12小时;微氧池中水力停留时间是18-30小时;好氧池中水力停留时间是13-17小时。 The denitrification reaction in the anoxic pond is carried out at PH=7.5-9.2, the dissolved oxygen (DO) is less than 0.5mg/L; the denitrification reaction in the anaerobic pond is at PH=7.0-8.5, the dissolved oxygen (DO) is carried out under the condition of less than 0.2mg/L; the denitrification reaction in the micro-aerobic pool is carried out at PH=7.4-8.3, and the dissolved oxygen (DO) is carried out under the condition of 0.5-1.0mg/L; in the aerobic pool The denitrification reaction is carried out at PH=6.5-8.0, dissolved oxygen (DO) at 2.0-4.0mg/L; the reflux ratio of the mixed solution is 100-300%; the hydraulic retention time in the anoxic pool is 7-14 hours The hydraulic retention time in the anaerobic pool is 9-12 hours; the hydraulic retention time in the micro-aerobic pool is 18-30 hours; the hydraulic retention time in the aerobic pool is 13-17 hours.
本发明的好处是:缺氧反硝化、厌氧氨氧化、短程硝化反硝化在同一生物处理系统中实现。实现短程硝化反硝化,节省25%的供氧量和40%的有机碳源 ,缩短反应停留时间,减少容积;实现厌氧氨氧化,降低能耗,防止二次污染;氨氮去除率高,达到99%以上;整个过程碱的消耗量减少,运行费用低。 The advantage of the invention is that anoxic denitrification, anaerobic ammonia oxidation and short-range nitrification and denitrification are realized in the same biological treatment system. Realize short-range nitrification and denitrification, save 25% of oxygen supply and 40% of organic carbon source, shorten reaction residence time, reduce volume; realize anaerobic ammonium oxidation, reduce energy consumption, and prevent secondary pollution; high ammonia nitrogen removal rate, reaching More than 99%; the consumption of alkali in the whole process is reduced, and the operating cost is low.
采用本发明可将COD为400-800mg/L、NH4+-N为150-450mg/L的氨氮废水降低为COD小于50mg/L,NH4+-N小于5mg/L,总氮小于15mg/L,低于国家一级排放标准。该工艺不仅大大提高了传统合成氨工业废水的脱氮效率,而且降低了运行费用,减少了占地面积。 The present invention can reduce ammonia nitrogen wastewater with COD of 400-800mg/L and NH4 + -N of 150-450mg/L to COD less than 50mg/L, NH4 + -N less than 5mg/L and total nitrogen less than 15mg/L. It is lower than the national first-level emission standard. This process not only greatly improves the denitrification efficiency of traditional synthetic ammonia industrial wastewater, but also reduces operating costs and floor space.
附图说明 Description of drawings
图1为合成氨工业废水中氨氮脱除方法流程图。 Fig. 1 is a flow chart of the ammonia nitrogen removal method in the synthetic ammonia industrial wastewater.
具体实施方式 Detailed ways
实施例1 Example 1
处理水量417m3/h,合成氨工业废水中COD含量约为600mg/L,氨氮含量约为350mg/L。合成氨工业废水先进入缺氧池中,与含有硝态氮(NO3 --N)的回流水混合进行脱氮反应,反硝化脱氮菌以废水中有机物作为电子供体,以硝态氮(NO3 --N)作为电子受体,在PH=7.5-9.2,溶解氧(DO)小于0.5mg/L条件下进行反硝化反应,使NO3 --N被还原为氮气(N2)脱除,缺氧池水力停留时间为12小时;脱氮之后的废水进入厌氧池,在厌氧池中与含有亚硝态氮(NO2 --N)的回流水混合进行厌氧氨氧化反应,以废水中的氨氮(NH4 +-N)做电子供体,以亚硝态氮(NO2 --N)为电子受体,在PH=7.0-8.5,溶解氧(DO)小于0.2mg/L条件下将NH4 +-N或NO2 --N转变成N2,厌氧池水力停留时间为9小时;含有NH4 +-N的废水进入微氧池,进行亚硝化反应,在PH=7.4-8.3,溶解氧(DO)在0.5-1.0mg/L条件下把NH4 +-N氧化为NO2 --N,同时含有NO2 --N的污水一部分回流到厌氧池,回流比为200%,微氧池水力停留时间为20小时;剩余的含有NO2 --N的废水进入好氧池,在PH=6.5-8.0,溶解氧(DO)在2.0-4.0mg/L条件下进行硝化反应,NO2 --N被氧化形成NO3 --N,含有NO3 --N的废水一部分通过回流到缺氧池进行反硝化脱氮,回流比为300%,好氧池水力停留时间为17小时,剩余废水进入沉淀池进行泥水分离,沉淀污泥回流到缺氧池进水端,污泥回流比为80%,处理出水达标排放。系统总的水力停留时间约为58小时,出水水质COD小于50mg/L,NH4+-N小于5mg/L,总氮小于15mg/L。 The treated water volume is 417m 3 /h, the COD content in the synthetic ammonia industrial wastewater is about 600mg/L, and the ammonia nitrogen content is about 350mg/L. The synthetic ammonia industrial wastewater first enters the anoxic tank, and mixes with the reflux water containing nitrate nitrogen (NO 3 - -N) for denitrification reaction. The denitrifying denitrification bacteria use the organic matter in the wastewater as the electron NO 3 - -N) as an electron acceptor, denitrification reaction is carried out under the condition of PH=7.5-9.2, dissolved oxygen (DO) is less than 0.5mg/L, so that NO 3 - -N is reduced to nitrogen (N 2 ) In addition, the hydraulic retention time of the anoxic tank is 12 hours; the wastewater after denitrification enters the anaerobic tank, and is mixed with the return water containing nitrite nitrogen (NO 2 - -N) in the anaerobic tank for anaerobic ammonia oxidation reaction , with ammonia nitrogen (NH 4 + -N) in wastewater as electron donor, nitrite nitrogen (NO 2 - -N) as electron acceptor, at PH=7.0-8.5, dissolved oxygen (DO) is less than 0.2mg NH 4 + -N or NO 2 - -N is converted into N 2 under the condition of /L, and the hydraulic retention time of the anaerobic tank is 9 hours; the wastewater containing NH 4 + -N enters the microaerobic tank for nitrosation reaction. PH=7.4-8.3, dissolved oxygen (DO) oxidizes NH 4 + -N to NO 2 - -N under the condition of 0.5-1.0mg/L, and part of the sewage containing NO 2 - -N is returned to the anaerobic tank, The reflux ratio is 200%, and the hydraulic retention time of the microaerobic pool is 20 hours; the remaining wastewater containing NO 2 - -N enters the aerobic pool, at PH=6.5-8.0, dissolved oxygen (DO) at 2.0-4.0mg/L Nitrification reaction is carried out under the conditions, NO 2 - -N is oxidized to form NO 3 - -N, part of the wastewater containing NO 3 - -N is returned to the anoxic pool for denitrification and denitrification, the reflux ratio is 300%, and the aerobic pool water The retention time is 17 hours. The remaining wastewater enters the sedimentation tank for mud-water separation, and the sedimented sludge returns to the water inlet of the anoxic tank. The sludge return ratio is 80%, and the treated effluent meets the standard discharge. The total hydraulic retention time of the system is about 58 hours, the effluent COD is less than 50mg/L, NH4 + -N is less than 5mg/L, and the total nitrogen is less than 15mg/L.
实施例2 Example 2
处理水量210m3/h,合成氨工业废水中COD含量约为450mg/L,氨氮含量约为250mg/L。合成氨工业废水先进入缺氧池中,与含有硝态氮(NO3 --N)的回流水混合进行脱氮反应,反硝化脱氮菌以废水中有机物作为电子供体,以硝态氮(NO3 --N)作为电子受体,在PH=7.5-9.2,溶解氧(DO)小于0.5mg/L条件下进行反硝化反应,使NO3 --N被还原为氮气(N2)脱除,缺氧池水力停留时间为7小时;脱氮之后的废水进入厌氧池,在厌氧池中与含有亚硝态氮(NO2 --N)的回流水混合进行厌氧氨氧化反应,以废水中的氨氮(NH4 +-N)做电子供体,以亚硝态氮(NO2 --N)为电子受体,在PH=7.0-8.5,溶解氧(DO)小于0.2mg/L条件下将NH4 +-N或NO2 --N转变成N2,厌氧池水力停留时间为9小时;含有NH4 +-N的废水进入微氧池,进行亚硝化反应,在PH=7.4-8.3,溶解氧(DO)在0.5-1.0mg/L条件下把NH4 +-N氧化为NO2 --N,同时含有NO2 --N的污水一部分回流到厌氧池,回流比为150%,微氧池3水力停留时间为25小时;剩余的含有NO2 --N的废水进入好氧池,在PH=6.5-8.0,溶解氧(DO)在2.0-4.0mg/L条件下进行硝化反应,NO2 --N被氧化形成NO3 --N,含有NO3 --N的废水一部分通过回流到缺氧池进行反硝化脱氮,回流比为200%,好氧池水力停留时间为13小时,剩余废水进入沉淀池进行泥水分离,沉淀污泥回流到缺氧池进水端,污泥回流比为100%,处理出水达标排放。系统总的水力停留时间约为54小时,出水水质COD小于50mg/L,NH4+-N小于5mg/L,总氮小于15mg/L。 The treated water volume is 210m 3 /h, the COD content in the synthetic ammonia industrial wastewater is about 450mg/L, and the ammonia nitrogen content is about 250mg/L. The synthetic ammonia industrial wastewater first enters the anoxic tank, and mixes with the reflux water containing nitrate nitrogen (NO 3 - -N) for denitrification reaction. The denitrifying denitrification bacteria use the organic matter in the wastewater as the electron NO 3 - -N) as an electron acceptor, denitrification reaction is carried out under the condition of PH=7.5-9.2, dissolved oxygen (DO) is less than 0.5mg/L, so that NO 3 - -N is reduced to nitrogen (N 2 ) In addition, the hydraulic retention time of the anoxic tank is 7 hours; the wastewater after denitrification enters the anaerobic tank, and in the anaerobic tank, it is mixed with the reflux water containing nitrite nitrogen (NO 2 - -N) for anaerobic ammonia oxidation reaction , with ammonia nitrogen (NH 4 + -N) in wastewater as electron donor, nitrite nitrogen (NO 2 - -N) as electron acceptor, at PH=7.0-8.5, dissolved oxygen (DO) is less than 0.2mg NH 4 + -N or NO 2 - -N is converted into N 2 under the condition of /L, and the hydraulic retention time of the anaerobic tank is 9 hours; the wastewater containing NH 4 + -N enters the microaerobic tank for nitrosation reaction. PH=7.4-8.3, dissolved oxygen (DO) oxidizes NH 4 + -N to NO 2 - -N under the condition of 0.5-1.0mg/L, and part of the sewage containing NO 2 - -N is returned to the anaerobic tank, The reflux ratio is 150%, the hydraulic retention time of the micro-oxygen pool 3 is 25 hours; the remaining wastewater containing NO 2 - -N enters the aerobic pool, at PH=6.5-8.0, dissolved oxygen (DO) at 2.0-4.0mg/ Under the condition of L, the nitrification reaction is carried out, NO 2 - -N is oxidized to form NO 3 - -N, part of the wastewater containing NO 3 - -N is returned to the anoxic tank for denitrification and denitrification, the reflux ratio is 200%, and the aerobic The hydraulic retention time of the pool is 13 hours. The remaining wastewater enters the sedimentation tank for mud-water separation, and the sedimented sludge returns to the water inlet of the anoxic tank. The sludge return ratio is 100%, and the treated effluent meets the standard discharge. The total hydraulic retention time of the system is about 54 hours, the effluent COD is less than 50mg/L, NH4 + -N is less than 5mg/L, and the total nitrogen is less than 15mg/L.
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