CA2185137C - Method of operating a sequencing batch reactor - Google Patents

Method of operating a sequencing batch reactor Download PDF

Info

Publication number
CA2185137C
CA2185137C CA 2185137 CA2185137A CA2185137C CA 2185137 C CA2185137 C CA 2185137C CA 2185137 CA2185137 CA 2185137 CA 2185137 A CA2185137 A CA 2185137A CA 2185137 C CA2185137 C CA 2185137C
Authority
CA
Canada
Prior art keywords
reactor
distributor
feed
fill
sludge
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CA 2185137
Other languages
French (fr)
Other versions
CA2185137A1 (en
Inventor
Kin Man Ho
Paul F. Greenfield
Kanthav Anam Subramaniam
Jurg Keller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CRC for Waste Management and Pollution Control Ltd
Original Assignee
CRC for Waste Management and Pollution Control Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CRC for Waste Management and Pollution Control Ltd filed Critical CRC for Waste Management and Pollution Control Ltd
Publication of CA2185137A1 publication Critical patent/CA2185137A1/en
Application granted granted Critical
Publication of CA2185137C publication Critical patent/CA2185137C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F3/00Biological treatment of water, waste water, or sewage
    • C02F3/02Aerobic processes
    • C02F3/12Activated sludge processes
    • C02F3/1205Particular type of activated sludge processes
    • C02F3/1221Particular type of activated sludge processes comprising treatment of the recirculated sludge
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/006Water distributors either inside a treatment tank or directing the water to several treatment tanks; Water treatment plants incorporating these distributors, with or without chemical or biological tanks
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/10Biological treatment of water, waste water, or sewage
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S210/00Liquid purification or separation
    • Y10S210/902Materials removed
    • Y10S210/903Nitrogenous

Abstract

A method of operating a sequencing batch reactor is described in which feed is supplied thereto by distributing feed into settled sludge in the bottom part of the reactor. A sequencing batch reactor having means for supplying feed to the bottom of the reactor is also described.

Description

Z 1 8 ~ 1 ,3 1 O 95124361 ~ PCT/AU95100118 METHOD OF OPERATING A SEQUENCING BATCH REACTOR
TECHNICAL FIELD
This invention relates to wastewater treatment and in particular to tre~tmrnt of w~ltwater using sequencing batch reactors.
S BACKGROUND ART
Meeting the h~creasingly stringent nitrogen (N) and phosphorous (P) effluent standards has had a major impact on the design and operation of wastewater treatment facilities dealing with domestic sewage with their typical unfavourable characteristics. Since the first success in achieving biological P
removal in a continuous full-scale biological N removal plant in the 1970's, incorporation of biological P removal in a biological N removal plant is considered to be a generally achievable objective. Design and operation of biological nutrient removal (BNR) plants are now required to optimise these two parallel but interactive processes to m~imice both nitrogen and phosphorus removal. Design and operation also requires simultaneous control of the ~csoci~tecl sludge bulking problems res~lting from the proliferation of fil~m~,ntous bacteria.
The available BNR processes can be divided into contim-ously and illt~ ltly operated systems. Continuously operated ~yShlllS comprise a number of separate tanks or ponds through which w~ltw~ler and sludge is passed in various ways. Intermittently operated systems use a single reactor or pond, somçtimes separated into zones by baffling, with only one pass of the w~ltwater through the reactor pond. Intermittent processes can therefore be chal~elised bytheir unique repeated sequencing time-oriented operation as collll)aled to the space oriented operation of the continuous processes.
Tntermittçntly operated ~y~ltms can be either fed continltolJcly or intermittently. They can be also subdivided into variable and constant volume systems. The variable volume systems accomplish solid-liquid sep~ tion in the same tank with subsequent withdrawal of the treated effluent (hltell.. illent decant) while the constant volume intermittently operated facilities c,arry that out by a 30 sep~rate in-series secontl~ry clarifier or basin with or without an underflow recycle ~l.l...i~-~, the activated sludge back to the process.
In the operation of intermittently fed sequencing batch reactors (SBR) or seque,ncing batch ponds (subsequently called reactors) a substantial proportion of WO 9S/24361 ~ 1 ~ S l 3 7 PCT/AU95/00118 the cycle time is used for the fill period. During this time, the part of the reactor volume that was discharged at the end of the previous cycle, is replaced by fresh sewage before aeration commences. In BNR operation of these reactors, the fill period is of major importance for the removal of both nitrogen and phosphorus S based nutrients. There are strong indications that good nutrient removal pelrol~llance is dependant on the structure and colllposilion of the biomass flocs in the reactors. Flocs should ideally be of similar size, compact, spherical and without filallle.ltous growth. This encourages simultaneous nitrification-denitrification during aeration periods and ensures good sludge settling plopellies.
10 Several advantages of simultaneous nitrification-denitrification have been reported in the past including reduced requirements for biodegradable carbon (or COD) in the raw wastewater, reduced aeration requirements and part or complete elimin~tion of anoxic reactors or sequences if net nitrate production can be kept at low levels.
Achieving simultaneous nitrification-denitrification is therefore regarded as 15 beneficial both in continuous and intermittent systems.
Existing technology such as the cyclic activated sludge system (CASS) uses so called selectors or contactors which are small volumes in the inflow part of the reactor. In these zones the inflowing feed is mixed with the return activated sludge which is pumped from the reactor bottom or from specific clarifiers. This has two 20 major drawbacks. Firstly, only part of the sludge mass is contacted with the inflowing feed and secontlly, it requires mechanical pumping of the sludge. Thissecond requirement is not only operationally difficult but is likely to have a negative effect on the structure of the sludge flocs due to the ...ecl-~-ic~l stress exerted during the pumping action.
25SU~MARY OF THE INVENI~ON
It is an object of this invention to provide a method of supplying feed to a sequencing batch reactor which allows m~intcn~nre of favourable floc characteri~tics and contributes to improved pelroll,lance of the reactor during periods following the fill period.
30The present inventors have surprisingly found that the manner in which feed is supplied to a sequencing batch reactor can effect floc formation and hence reactor pelrol~ nce In particular, the inventors have found that even distribution of feed into the settled sludge bed can improve reactor pclru~"~nce. This _ ~O 95/24361 218 513 7 PCT/AU95/00118 3 ; .~
improvement is enh~nced by including a non-mixed period into the FILL period of the reactor cycle.
In one aspect, the invention provides a method of supplying feed to a sequencing batch reactor, said method colllylising distributing feed into settled 5 sludge in the lower part of the reactor.
Feed can be distributed via a static distributor or a mobile distributor and can be supplied without mixing of reactor collttl,ts during at least a portion of, or throughout, the reactor fill period.
In a second aspect, the invention provides a sequencing batch reactor 10 COIllyliSillg at least one reactor vessel having feed means, aeration means, decant means and, optionally, mixing means; wherein said feed means colllylises at least one distributor located at the bottom of said reactor vessel.
As in the method accordhlg to the first aspect, the reactor distributor can be a static or mobile distributor. Static distributors typically comprise a manifold 15 suppling a plurality of distributor outlet lines. Alternatively, a static distributor can be a manifold with an e~tcn-led upper surface having a plurality of outlets therein.
Mobile distributors typically comprise a member having a plurality of outlets therein which moves either linearly along the bottom of the reactor vessel or rotates about an axis vertically disposed with respect to the bottom of the 20 reactor.
Other aspects of the invention will become appalGlll from the following detailed descliytion.
BRIEF DESCRIPIION OF THE DRAWINGS
Figure 1 is a ~c~cselltation of the system used for laboratory scale 25 evaluation of the method according to the invention.
Figure 2 presents influent and effluent concelllldlions in a laboratory scale SBR opcrath~g over a 5 month period.
Figure 3 depicts the cyclic pclrollllance of the laboratory scale SBR.
Figure 4 depicts concentration profiles of nitrogen compounds during the 30 non-mixed FILL period of a laboratory scale SBR with respect to reactor height.
Figure 5 depicts phosphorous concentration profiles during the non-mixed FILL period with respect to reactor height of the same SBR the subject of Figure4.

WO 95/24361 21 8 ~ 7~ - PCT/AU95/00118 Figure 6 is a diagrammatic representation of an SBR.
DETAILED DESCRIP~ION OF THE rNVENllON
The following abbreviations are used herein:-BASS batch activated sludge system;
BNR biological nutrient removal;
BPR biological phosphorous removal;
CASS'~ cyclic activated sludge system;
COD chemical oxygen dem~n~l;
DO dissolved oxygen;
F/M food/microorganisl,l ratio;
N nitrogen;
NAS non-agitated sequence;
NH4-N ammonium nitrogen;
NO2-N nitrite nitrogen;
NO3-N nitrate nitrogen;
NOX-N the sum of nitrite nitrogen and nitrate nitrogen;
OUR oxygen uptake rate;
PO4-P phosphate phosphorous;
P phosphorous;
RBCOD readily biodegradable chemical oxygen dçm~n-l;
SBR sequencing batch reactor;
So/Xo ratio of the initial substrate concentration to the initial biomass concentration;
TCOD total chemical oxygen dç~n~nd;
TKN total Kjeldahl nitrogen;
TP total phosphorous.
The term "sequencing batch reactor", abbreviated "SBR", as used in the following description and claims is not nçcçss~.jly restrieted to ~y~lems which are commonly called SBRs and includes any intermittently ope~ated aerobic wa~ vatel 30 treatment system colll~lisillg as a process step settling of sludge within the reactor vessel. The scope of the appended claims is not therefore restricted to SBRs per se and the method of the invention is applicable to any in~çrmittçn~ly operated aerobic wa~l~atcr treatment system co~ sing as a process step settling of sludge within ~ J
0 95t24361 ~ l V ' PCT/AU95/00118 s the reactor vessel.
Seque~sing batch reactors (SBRs) require a non-~gitAtçd (non-mixed and non-aerated) SETTLE period to accomplish solid-liquid separation in the same tank with subsequent withdrawal of the treated effluent (intermittent decant), i.e.
5 variable volume operation. During this non-agitated sequence (NAS), the biomass is allowed to conccllt~ate at the bottom of the reactor and form a clear SUP~ AIA~
It is the çxtcn~ion of this special feature, which can be incorporated in an ope~aling strategy not only for solid-liquid separation but more i..lpo.lalltly for biosorption of the biodegradable organics and rapid environmental changes, which10 makes p~ ...ance of the present reactor system superior to all co..v~llLional SBRs and continuous systems in terms of carbon, carbon and nitrogen, and carbon, nitrogen and phosphorus removal with positive sludge bulking control. This formsthe basis of the present invention.
A typical SBR cycle is divided into five discrete time periods: FILL, 15 REACT, SEITLE, DRAW and IDLE. With further combination of mixed or non-mixed and aerated or non-aerated operation, a total of 12 dirrcrtnt reactions are possible.
The FILL period is the period of feed input into the reactor whe~as the REACI period is a period of reaction without addition of fresh wa~Levvatel. In 20 ~cco-dance with the invention, feed to the reactor during the FILL period is evenly distributed through the settled sludge bl~nkçt.
An SBR cycle is typically within the range of 2 to 24 hours. Ideally, a cycle is less than 8 hours provided that reactor throughput is not colllp~olllised by the shorter cycle time. The following table sets out a typically opelaling ~Llate~y 25 and is based on a 6 hour cycle time.
TABLE I
Typical Operating Strate~y Reaction Sequence Time (h) 1. Non-mixed FILL 1.25
2. Mixed FILL 1.25
3. Aerated mixed REACT 1 1.00 WO 95/24361 ~ 1 8 5 1 3 7 PCT/AU95/00118
4. Non-mixed REACT 0.50
5. Aerated mixed REACT 2 1.50
6. SETTLE 0.33
7. DRAW 0.17
8. IDLE 0.00 TOTAL 6.00 The most hllpoll~,lt non-mixing sequence in iete~ g good process 10 pelrollllance and sludge characteristics is the non-mixed FILL sequence. With an applopliate feeding pattern, interrelated chain reactions leading to excellent process pelrolll,ance with good sludge settling characteristics can be initi~ted The subseque~t non-mixed non-aerated REACT sequences further ensure that these chain reactions proceed in the required direction, çspec;~lly for h~nllling carbon-15 deficient/nutrient-rich wastewaters. In both cases, the concentrated biomass at the bottom of the reactor allows more rapid development of any required environm~nt~l conditions either from anoxic to anaerobic or from aerobic to anoxic.
In the non-mixed FILL sequence, the method according to an embodiment 20 of the invention is to introduce and distribute the incoming wasltwattr through the settled sludge blanket allowing intim~te contact bGl~,en the conce"tlaled biomass and the undiluted incolllillg wa~ valer. Generation of localised high So/Xo ratios and self-adjusting floc loading allows rapid biosorption by the floc-forming bacteria. The enmeshment of the slowly biodegradable particulate COD under 25 anaerobic conditions further allows more RBCOD to be ge"e,ated by fermentation and erlh~nres biological phosphorus removal without incorporating any ~fllllaly sludge prefermentor. This is particularly desirable as the RBCOD concentration of some domestic wastewaters is around 25 to 50 mg L-l.
A second important environmental condition created by such a feeding 30 pattern is the development of a high NH4-N concentration. As the influent wa~l~wal~,r in the method of the invention is slowly fed to the reactor floor without gentlalillg any significant mech~nic~l mixing, the treated effluent in the sludge blanket from the previous cycle is gradually replaced by the influent wastewater.
Furthermore, it was found that the level of biodegradable carbon required for the ~0 95/24361 2~1 8 5 1 3 7 PCT/AU95/00118 denitrification process can be subst~nti~lly reduced by use of the innovative feeding and operational strategy presented in this invention. A ratio of TCOD:TKN below the commonly reported minim~l value of 7 for the influent v~ lt~v~ter was found to be suitable in this situation to achieve a high degree of nitrogen removal. As the 5 TCOD:TKN ratio of domestic wastewater is very often ~10 and frequently <7, this subst~nti~l saving in carbon source provides high potential in achieving future hlcl~asingly stringent effluent standards without any external addition of carbon.
Furthermore, in a single-tank system, i.e. wilholll recycle, m~ g Iow effluent NO3-N concentration in BASS relies on simultaneous nitrification-10 denitrification during the aerated sequence. This process is believed to depend onthe formation of an anoxic fraction within the flocs which relies not only on the bulk DO concentration (0.5 to 3 mg L-'), but more importantly on the floc characteristics .
The activity of the biomass in terms of the OUR or m~ specific 15 growth rate and the floc ~ meter can be controlled by introducing the above-mentioned innovative feeding pattern during the non-mixed FILL with subsequ~nt endogenous anaerobic sludge stabilisation resulting from achieving good simlllt~nloQus nitrification-denillirication. By imposing such altç l.~t;..g feast and famine environments, bacteria in the activated sludge culture capable of rapid 20 enzymatic transport of soluble organic substrates under exogenous an,,erobic conditions, and synchronous multiplication in the presence of molecular oxygen, will be selected. This leads to a high OUR and full restoration of the biosorptive capacity in the endogenous aerobic and anaerobic periods. Filaments which are slower substrate accumulating and incapable of denitrifying and polyP
25 ~c~lmul~ting will be eliminated. Fast growing, starvation-susc~ptihle filamentous org~ni~m~ will also be removed during the ç~tçn-led period of endogenous metabolism. This mode of operation ensures a high OUR especi~lly at the - beginning of the aerobic period and good settling biological flocs of optimal size to facilitate simultaneous nitrification-denitrification of the wastewater.
30 Consequently, simultaneous nitrification-denitrification is enhanced. The resulting pH gradient due to nitrification and rapid uptake of phosphate further enh~nc~
simultaneous nitrification-denitrification even at higher DO concentration.
With successful simultaneous nitrification-denitrification, the reaction WO 95/24361 ~18 S 13 7 ` ~ PCT/AU95/00118 conditions required to achieve biological nitrogen and phosphorus removal changefrom anaerobic/anoxic/aerobic as in continuous BNR systems to anaerobic/aerobic only. This elimin~tes the presently unavoidable and uncontrollable sludge bulking problems due to alternating anoxic-aerobic conditions and the adverse effects on5 biological phosphorus removal caused by the carbon deficiency associated with incomplete denitrification.
It is believed that one of the major advantages the fil~mentous bacteria can have over the floc-forming bacteria is the way of growth of the former in the mixed liquor. The filamentous bacteria grow in profusion beyond the confines of 10 the floc into the bulk medium bridging between flocs or completely in high abundance in the bulk solution. Consequently, they compete well with the floc-forming bacteria in completely mixed systems by having a larger surface area andlower substrate affinity. However, this privilege is no longer available if the feed is directed to the well thickened sludge after a prolonged SETIIE period which is 15 nonn~lly not available in continuous clarifier systems. Another possible çYp!~n~tion of their way of growth is that the environmental conditions inside the floc are unfavourable. Consequently, they tend to extend their structure from the floc particularly to i"tclrG~G with compaction during settling. Forcing them back to the floc during the SEITLE and non-mixed FILL period subst~nti~lly reduces their20 chance of CQInreting with the floc-formers.
The major benefit of this feed system into the reactors, is the i~ nsive contacting of all biomass with the fresh feed stream entering the reactor. A large part of the water in the reactor from the previous cycle is in the supe,llatallt and thelGfole not in contact with the sludge. This is advantageous since the supelllal~nt 25 water often contaills nitrates which can be dehi,llental to the pGlrullllance of the phosphorous removal processes.
This c~nt~cting period also provides a high food/microor~allislll ratio (F/M) which is beneficial for the growth of desirable floc-forming bacteria. Moreover,the presence of readily biodegradable chemical oxygen dcrn~nd (RBCOD) favours 30 the accumulation of internal carbon sources in the phosphorous removing bacteria.
This stored carbon is then used in the phosphate uptake process during the aeration period and therefore facilitates the phosphorous removal process.
A major advantage of the present system is that the whole treatment process o 95/2J361 218 513 7 PCT/AU95/U0118 can be done in one single vessel. The auxiliary equipment needed is also minim~lsince only feed and possibly a draw pump (and clec~ting weir), air blower and a mechanical mixer are needed to operate the reactors. In a minim~l configuration,outflow (draw) can be achieved by a simple overflow me~ and me~h~nic~l S mixing might not be necess~ry in all cases.
C'~...l.~ed to e~icting contim~ous and i.~ BNR plants this design offers subst~nti~lly reduced capital costs, simple operation and, based on the results obtained to date, excellent tre~tm~nt pelr(~ nce in regards to COD, total N and total P. Experiments also show that it can handle very high strength wastewater (N
and P) which is common in industrial tre~tmPnt systems.
Although similar non-mixed fill sequences have been used in sequencing batch reactor cycles prior to this invention, the objectives of the use were dirr~lent and the substantial benefits offered by such a simple modification were ignored.Chiesa et al (Biotechnology and Bioengineering 27, 562-569, 1985) carried out bench-scale studies using the non-mixed FILL sequenre to gc.leldte substrate gradient for their feast/famine population selection in sludge bulking control. In the c;~ lh~ents conducted by Manning and Irvine (Journal of Water Pollution Control Federation, 59(1), 13-18, 1985), the non-mixed FILL sequence was i"col~o,~ted in the control system to minimi~e the contact betv~,~en the biomassand the organic substrates while a mixed dump-FILL sequence was used to develop phosphorus removal sludge. The non-mixed FILL sequence was also trialled by Oomori et al. (Proceedings of the Australian Water and Wastewater Association 13th Federal Convention, pp. 359-363, 1989) as an operating strategyin their pilot studies. Full-scale operation using this reaction sequence included Irvine et al. (Journal of Water Pollution Control Federation, 57(8), 847-853, 1985);
K~tc~llm et al. (Journal of Water Pollution Control Federation, 59(1), 13-18, 1987) and Nielson and Thompson (Journal of Water Pollution Control Federation 60(2), 199-205, 1988). However, none of the prior art describes or hints at supply of feed to the reactor by direct and even distribution to the settled sludge blanket during the non-mixed FILL sequence.
So that the invention may be better understood, non-limiting examples follow.

WO 9S/24361 218 5 1 3 7 j " - ~ PCTIAU95/00118 l~e method of the invention was applied to abattoir (~ ghter house) wa5lt~vdter high in both nutrients and carbon. The feed used in this laboratory-scale study was effluent from an anaerobic pond of an abattoir w~t~ ,ttr system.SThe SBR was operated at room tempe~atul~ (20 + 2C) with an hydraulic retention time and solids retention time of 1.5 days and 20 days l~,s~eclively. The reactor had a volume of 4.5 L and feed was distributed beneath the sludge blanket via a tube tçrmin~ting at the bottom of the reactor vessel near the centre thereof.
The reactor was seeded with sludge from a nitrogen removing clomestic sewage 10treatment plant. The reactor sequence periods are set out in Table II while the physical aspects of the process are shown in Figure 1.
TABLE II
Reactor Sequence Periods Time (h) Reaction SequenceExperimental Phase 1Experimental Phase 2 Non-mixed Fill 2.S 2.5 Aerated mixed React 1 3.0 1.0 Non-aerated mixed React 0 0.5 Aerated mixed React 2 0 1.5 Settle 0.33 0.33 Draw 0.17 0.17 Grab samples of wastewater were collected once every S to 7 days and were 30 stored under anaerobic conditions at 4C. Influent wastewater from a feed drum was intermittently fed to the system at a rate of 400 mL h-', by a variable-speed Masterflex pump. Effluent discharge was by gravity. Mixing was provided by a m~etic stirrer. Diffuser stones were used to distribute air to the reactor. Excess activated sludge wasting was pGlrollned in every cycle at the end of the aerated35 mixed REACT 2 period to m~int~in the sludge age. All operations (i.e. fill, aeration, mixing and effluent discharge) were controlled by an IBM colnpatible 21~5137 _ O9S/24361 ~ PCT/AU95/00118 co. . .ru~cr.
The p~lrollllance of the reactor, as determined from the daily influent TKN
and PO4-P, and effluent NO,-N and PO4-P, iS presented in Figure 2. In Figure 2, the following symbols are used: influent PO4-P, closed circle; influent TKN, 5 closed triangle; efflnerlt NO,-N, open triangle; and, effluent PO4-P, open circle.
After 105 days, the OpClatillg conditions were ~ h~nged slightly, incorporating a 30 min1Jtes non-aerated mixing sequence after one hour of aeration period (Phase 2 of Table II). This was based on an analysis of the cyclic behaviour of the reactor at day 95.
Figure 2 clearly shows that the reactor achieved a very high degree of nutrient removal, particular in respect of PO4-P. Once the BNR system was established, col~;cle~ y low levels of phosphate were recorded in the effluent. For a period of over two months, each daily phosphate measu~lllent was below the detection limit of the analytical method used (ion chromatography) which is at least 15 0.5 mg/L PO4-P. This result could be m7int~ined even under large fluctuations in the influent P conce~l alion reaching 60 mg/L PO4-P in some ~mrles The çfflnent COD and TKN conccntl~lions were belweell 100-200 mg/L and 5-14 mg/L It;s~e~ /ely.
These results show the very high capacity of this system and the stability of 20 the BNR processes once established. It is believed that this stability is based on the development of a particular biomass floc structure which could be essçnti~1 to achieve simultaneous nitrification/denitrification (SND). This enables co..c~ t NO,-N effluent conccllllations below 15 mg/L which in turn is l~e~ss,.~ to achieve complete anaclobic conditions in the FILL period. ~n~equçntly, the P
25 removing olg~ni~ c are not copeli.~g with denitrifiers for the hlcolllillg RBCOD
which results in high carbon accumulation and phosphate release by these micro-o~ The measured SVI values in the reactor reln~ined below 100 mVg at all times, providing further evidence that the flocs in this system are of a colll~acl, dense structure.
The cyclic pelroll,lance of the reactor was ~sessed and the results of this e~ ,.h"ent are pltisellled in Figure 3. Operational conditions were the same as detailed above with the exception that the FILL period co"lplised a 2 hour non-mixed FILL followed by a 30 minute mixed FILL. In Figure 3, plots of NH4-N, WO 95/24361 ~ 1 8 51 3 7 ; PCT/AU9~/00118 .; , :,, ~, .

NO,~-N and PO4-P concentrations are indicated by diamonds, squares and triangles, .,specli~rely.
Figure 3 shows that the high SJXo ratio generated by incorporating a non-mixed FILL sequence at the be~ of a cycle allows simultaneous nitrifi~tion-S de~ irlcation with the in-reactor NO,~-N co.-~ f l~ation being less than S mg~L
during the entire air-on sequences. It can be seen the NO,~-N concentration at the end of the cycle was low which greatly e~h~n~d allae~obic RBCOD uptake and P
release. The highest P04-P in the sludge blanket recorded was 56 mg/L.
However, PO4-P uptake in the presence of DO was rapid and complete çlimin~tion0 of PO4-P was achieved during the second aerated mixed R_ACT (Figure 3).

Experiments were conducted to assess conce~t~dlion profiles over reactor height during the non-mixed FILL period of an SBR. A laboratory scale SBR of 12 L volume was used and the process run with a 18 hour hydraulic retention timeand 20 day sludge age in a tempeldtlJre controlled room (20 + 2C). The w~ltwdler used in this e~. ,i,l,cnt was raw sewage from a domestic sewage llca~ plant. The FILL period was 2.5 hr without mi~ing, Feed was supplied via a tube termin~ting with a T-piece. The arms of which distributed feed evenlyinto the settled sludge at the bottom of the reactor. Other operational conditions were generally as described above in FY~mrle 1. Samples were taken at various times after feeding had been initiated and either at the reactor bottom or from various heights above the reactor bottom.
Results are presented in Figures 4 and 5. In Figure 4, NH4-N (tri~ngles), NO3-N (squares) and NO2-N (diamonds) concc"l,dtions are shown for samples taken 10 min (open symbols), 1 hr 15 min (stippled symbols) and 2 hr 25 min (filled symbols) after feeding. PO4-P concentrations presented in Figure 5 are similarly of samples taken at 10 min (open symbols), 1 hr 15 min (stippled symbols) and 2 hr 25 min (filled symbols) after feeding.
The purpose of the non-mixed FILL sequence is to allow the biomass to thicken to a high co"cc"l,dtion at the bottom of the reactor, with the liquid forming a clear supellldtdnt. The NO,~-N rem~ining from the previous cycle is quickly removed in the sludge blanket due to the high biomass and substrate conce"l,dtion in that part of the reactor (Figure 4). The latter condition results from distributing _, O 95/24361 2 1 8 5 1 3 7 PCT/AU95/00118 the feed at the bottom of the reactor. After establishment of truly anaerobic conditions, instead of anoxic conditions, in the sludge blanket a high anaerobic P
release by the BPR bacteria can be observed (Figure 5).

In this example, an SBR is described in which feed is distributed at the bottom of a reactor vessel. The SBR will be exemplified with lcftl~nce to Figure6 which diagrammatically depicts a pilot SBR plant comprising two 10,000 L
reactor vessels. SBR's conveniently comprise two reactor vessels so that with staggered cycles of operation, supply of wastewater to the SBR is essenti~lly c(!ntinllQus.
Referring to Figure 6, there is shown SBR 1 Co~ liSillg reactor vessels 2 and 3. SBR 1 includes a feed distributor for each vessel. With reference to reactor vessel 2, components of distributor 4 are pump 5, which supplies feed tomanifold 6 mounted above the vessel. Manifold 6 feeds a plurality of drop tubes,one of which is indicated at 7. The drop tubes each tçrrnin~te in a distributor pipe, one of which is indicated at 8. Each distributor pipe includes a plurality of upwardly directed outlets.
It will be appreciated that distributor 9 of reactor vessel 3 co...~ es the same colll~onents as distributor 4.
During a FILL period, feed is delivered to the distributor via the pump.
Feed exiting distributor pipe outlets allows even distribution of the feed through settled sludge in the bottom of a reactor vessel.
It should be appreciated that various other cll~nges and modifications can be made to the embodiments exemplified without departing from the spirit of the invention which is limited only by the scope of the claims appended hereto.

Claims (9)

14
1. A method of operating a sequencing batch reactor having a cycle consisting of FILL, REACT, SETTLE and DRAW periods and optionally an IDLE
period, wherein supply of feed to the sequencing batch reactor comprises evenly distributing the feed throughout settled sludge via a distributor located at the bottom of a reactor vessel comprising said reactor; wherein said feed is supplied without mixing of reactor contents during at least an initial portion of the reactor FILL period, and said distributor is selected from:
(a) a static distributor configured to distribute feed over said vessel bottom; or (b) a mobile distributor capable of moving over said vessel bottom.
2. Method according to claim 1, wherein said distributor is a static distributor.
3. Method according to claim 1, wherein said distributor is a mobile distributor.
4. Method according to claim 1, wherein feed is supplied without mixing of reactor contents during all of the reactor FILL period.
5. Method according to claim 1, wherein said reactor comprises two reactor vessels each having a distributor, aeration means, decant means and, optionally, mixing means.
6. Method according to claim 2, wherein said static distributor comprises a manifold supplying a plurality of distributor outlet lines.
7. Method according to claim 2, wherein said distributor comprises a manifold with an extended upper surface having a plurality of outlets therein.
8. Method according to claim 3, where said mobile distributor comprises a member having a plurality of outlets therein, which member moves linearly along the bottom of said reactor vessel.
9. Method according to claim 3, wherein said mobile distributor comprises a member having a plurality of openings therein, which member rotates about an axis vertically disposed with respect to the reactor vessel bottom.
CA 2185137 1994-03-11 1995-03-10 Method of operating a sequencing batch reactor Expired - Fee Related CA2185137C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AUPM4355A AUPM435594A0 (en) 1994-03-11 1994-03-11 Method of operating sequencing batch reactors
AUPM4355 1994-03-11
PCT/AU1995/000118 WO1995024361A1 (en) 1994-03-11 1995-03-10 Method of operating a sequencing batch reactor

Publications (2)

Publication Number Publication Date
CA2185137A1 CA2185137A1 (en) 1995-09-14
CA2185137C true CA2185137C (en) 2002-01-22

Family

ID=3778971

Family Applications (1)

Application Number Title Priority Date Filing Date
CA 2185137 Expired - Fee Related CA2185137C (en) 1994-03-11 1995-03-10 Method of operating a sequencing batch reactor

Country Status (8)

Country Link
US (1) US5525231A (en)
KR (1) KR100304842B1 (en)
CN (1) CN1098218C (en)
AU (1) AUPM435594A0 (en)
CA (1) CA2185137C (en)
MY (1) MY115342A (en)
NZ (1) NZ282330A (en)
WO (1) WO1995024361A1 (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5853589A (en) * 1996-06-05 1998-12-29 Eco Equipment Fep, Inc. Advanced biological phosphorus removal using a series of sequencing batch reactors
EP0866033A3 (en) * 1997-03-18 2001-07-11 Ken Haggerty Process for the biological treatment of waste water
US6383389B1 (en) 2001-02-15 2002-05-07 United States Filter Corporation Wastewater treatment system and method of control
US6697740B2 (en) 2002-02-19 2004-02-24 William G. Smith Method and system for real-time control of sampling instruments in a batch operation
KR100456409B1 (en) * 2002-05-14 2004-11-10 주식회사 파세코 Fermentability control method of kimchi-refrigerator
MY136835A (en) * 2002-06-28 2008-11-28 Kingsford Environmental H K Ltd Combined activated sludge-biofilm sequencing batch reactor and process
GR20050100268A (en) * 2005-05-31 2006-12-18 Γερασιμος Λυμπερατος Standard reactor for biological removal of nitrogen from liquid waste by avoiding ths production of nitrates
CN100436343C (en) * 2005-12-28 2008-11-26 中国科学院生态环境研究中心 Circulation type double fluid state sewage treatment reactor
US7837955B2 (en) * 2006-03-08 2010-11-23 Unimin Corporation Continuous reactor system for anoxic purification
HU230285B1 (en) 2011-09-19 2015-12-28 UTB Envirotec Környezettechnológiai Zrt. Modified continuos flow sequencing batch reactor and a method for treating waste water
JP5963668B2 (en) * 2012-12-27 2016-08-03 オルガノ株式会社 Wastewater treatment method
KR20160008502A (en) 2013-03-14 2016-01-22 디.시. 워터 앤 수어 오쏘러티 Method and apparatus for maximizing nitrogen removal from wastewater
CN109694132B (en) * 2019-02-23 2021-12-17 何江涛 Sewage treatment method of sequencing batch temperature and pressure control biological membrane
CN115010250B (en) * 2022-01-21 2023-07-07 滁州职业技术学院 Mud-resistant biological anaerobic reactor for sewage treatment
CN114506922B (en) * 2022-03-02 2023-04-25 山东问清环境科技有限公司 Unpowered constant-water-level automatic drainer and drainage method thereof

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4596658A (en) * 1984-01-30 1986-06-24 Mandt Mikkel G Sequencing batch reactor decanter systems
US4755296A (en) * 1985-03-21 1988-07-05 Occidental Chemical Corporation Integrated biological-adsorption process for treating waste water
US4623464A (en) * 1985-03-21 1986-11-18 Occidental Chemical Corporation Removal of dioxins, PCB's and other halogenated organic compounds from wastewater
US4775467A (en) * 1985-09-20 1988-10-04 Calltharp Glen R Reactor piping with pump column
JPS62149399A (en) * 1985-12-24 1987-07-03 Ebara Infilco Co Ltd Treatment of organic sewage
US5013441A (en) * 1988-07-20 1991-05-07 Goronszy Mervyn C Biological nutrient removal with sludge bulking control in a batch activated sludge system
US4883602A (en) * 1988-08-22 1989-11-28 Fluid Dynamics, Inc. Decanting apparatus and method
JPH02284696A (en) * 1989-04-25 1990-11-22 Hitachi Plant Eng & Constr Co Ltd Batch-type activated sludge treating device
US4997557A (en) * 1989-05-19 1991-03-05 Aqua-Aerobic Systems, Inc. Floating, mixing, aerating and decanting unit
US5021161A (en) * 1990-02-16 1991-06-04 Jmo Holding, Inc. Method for the treatment of wastewater
US5126050A (en) * 1990-05-10 1992-06-30 Sbr Technologies, Inc. Granular activated carbon-sequencing batch biofilm reactor (GAC-SBBR)
CA2041329C (en) * 1991-04-26 1994-05-24 Brian H. Topnik Sequencing batch reactors
US5185079A (en) * 1991-05-16 1993-02-09 Iowa State University Research Foundation, Inc. Anaerobic sequencing batch reactor
US5186821A (en) * 1991-09-03 1993-02-16 D. Thomas Murphy Wastewater treatment process with cooperating velocity equalization, aeration and decanting means
JPH05192687A (en) * 1992-01-22 1993-08-03 Inax Corp Batch type sewage treatment
US5205936A (en) * 1992-02-05 1993-04-27 Bio Clear Technology Inc. Sequencing batch reactors
US5395527A (en) * 1993-07-01 1995-03-07 Eco Equipement Fep Inc. Process and apparatus for treating wastewater in a dynamic, bio sequenced manner

Also Published As

Publication number Publication date
KR100304842B1 (en) 2001-11-22
CA2185137A1 (en) 1995-09-14
NZ282330A (en) 1998-08-26
CN1098218C (en) 2003-01-08
CN1143941A (en) 1997-02-26
AUPM435594A0 (en) 1994-03-31
MY115342A (en) 2003-05-31
KR970701676A (en) 1997-04-12
US5525231A (en) 1996-06-11
WO1995024361A1 (en) 1995-09-14

Similar Documents

Publication Publication Date Title
Van Loosdrecht et al. Upgrading of waste water treatment processes for integrated nutrient removal—The BCFS® process
CA2185137C (en) Method of operating a sequencing batch reactor
US6485645B1 (en) Biological process for removing phosphorus involving a membrane filter
CA2083199C (en) Method for the treatment of sewage and installation to be used for this method
EP0603316B1 (en) Method and system for biologically removing nitrogen from wastewater
US5288405A (en) Wastewater treatment with enhanced biological phosphorus removal and related purification processes
US6926830B2 (en) Combined activated sludge-biofilm sequencing batch reactor and process
US5380438A (en) Treatment of wastewater through enhanced biological phosphorus removal
US5543051A (en) Biological phosphorus removal from waste water
WO1998001397A1 (en) Multi-phase dual cycle influent process
KR100436186B1 (en) Municipal Wastewater Treatment Apparatus and Process with a Continuous Feed and Cyclic Aeration
EP0885175A1 (en) System for removing nutrients from wastewater
JP2659167B2 (en) Sewage denitrification dephosphorization method and apparatus
WO2005014485A2 (en) Chemically enhanced primary sludge fermentation method
CA2300719A1 (en) Membrane supported biofilm process
CN101402488B (en) CAST segmenting water feed reinforced denitrification control method
GB2228930A (en) Removal of nitrogen and phosphorus from sewage
EP0849230A1 (en) Dual-stage biological process for removing nitrogen from wastewater
JPS5573398A (en) Biological denitrification and dephosphorization of waste water
EP1112968A1 (en) Soil water activated sludge treating system and method therefor
WO2013041893A1 (en) Modified continuous flow sequencing batch reactor and a method for treating waste water
AU682101B2 (en) Method of operating a sequencing batch reactor
Hayakawa et al. Simultaneous nitrogen and phosphate removal by the intermittent cyclic process
KR100438323B1 (en) High intergated Biological Nutrient Removal System
PL158608B1 (en) Method of and apparatus for treating waste waters containing organic substances, in particular for efficient removal of phosphorus and nitrogen

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed