Water Treatment Method for Simultaneous Abatement of Carbon, Nitrogen and Phosphorus, Implemented in a Sequencing Batch Moving Bed Biofilm Reactor
20220017392 · 2022-01-20
Assignee
Inventors
- Aude FOURCANS (Villepieux, FR)
- Philippe ZOZOR (Verneuil Sur Seine, FR)
- Tristan GERMAIN (Castelginest, FR)
- Hugues Humbert (Claye Souilly, FR)
- Romain LEMAIRE (Vernou Sur Brennes, FR)
Cpc classification
Y02W10/10
GENERAL 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
C02F3/307
CHEMISTRY; METALLURGY
C02F3/301
CHEMISTRY; METALLURGY
International classification
Abstract
Water treatment method for simultaneous abatement of carbon, nitrogen and phosphorus, implemented in a sequencing batch moving bed biofilm reactor (SBMBBR) comprising carriers suitable for the development of a biofilm. The method comprises sequences of successive treatments, each treatment sequence comprising:
an initial phase of anaerobic treatment,
said initial phase of anaerobic treatment being followed by at least one aerobic/anoxic cycle consisting of: an aerobic treatment phase so as to obtain an ammonium ion concentration that does not pass below a threshold concentration of ammonium ions; and
a phase in which the biofilm is placed, at least locally, under anoxic conditions, this phase being concomitant with or posterior to said aerobic treatment phase; the threshold concentration of ammonium ions being calculated to allow the development of Anammox microorganisms during the phase in which the biofilm is placed, at least locally, under anoxic conditions.
Claims
1. Water treatment method for simultaneous abatement of carbon, nitrogen and phosphorus, implemented in a sequencing batch moving bed biofilm reactor (SBMBBR) comprising carriers suitable for the development of a biofilm, said method comprising sequences of successive treatments, each treatment sequence comprising: an initial phase of anaerobic treatment, said initial phase of anaerobic treatment being followed by at least one aerobic/anoxic cycle comprising: an aerobic treatment phase so as to obtain an ammonium ion concentration that does not pass below a threshold concentration of ammonium ions; and a phase in which the biofilm is placed, at least locally, under anoxic conditions, this phase being concomitant with or posterior to said aerobic treatment phase; the threshold concentration of ammonium ions being calculated to allow the development of anammox microorganisms during the phase in which the biofilm is placed, at least locally, under anoxic conditions.
2. Method according to claim 1, wherein the threshold concentration of ammonium ions is ≥1 mg N/L.
3. Method according to claim 1 wherein, for each treatment sequence the SBMBBR has a volume exchange ratio (ERV) between 90% and 100%.
4. Method according to any one of claim 1, wherein for each biological treatment cycle, the anaerobic treatment phase lasts from 30 minutes to 5 hours and the at least one aerobic/anoxic cycle lasts from 1 hour to 10 hours.
5. Method according to any one of claim 1, wherein for each cycle of the at least one aerobic/anoxic treatment cycle, the phase in which the biofilm is placed under anoxic conditions is posterior to the aerobic phase, and the ratio between the duration of the aerobic phase and the total duration of the aerobic-anoxic phase is between 0.2 and 0.8.
6. Method according to claim 1, wherein said carriers are capable due to their geometry to remain in close proximity to each other when the aeration intensity is moderate, thus forming local anoxic conditions during an aerobic treatment phase.
7. Method according to claim 1, wherein there is no pre-seeding with anammox microorganisms and denitrifying polyphosphate accumulative organisms (DPAOs).
8. Method according to any one of claim 1, wherein there is no addition of an external source of carbon and/or there is no addition of an external source of metal salts.
9. A method of biologically treating water containing carbon, nitrogen and phosphorus and removing carbon, nitrogen and phosphorus from the water, comprising: directing the water into an SBMBBR containing biofilm carriers; subjecting the water to sequences of successive treatments in the SBMBBR, each treatment sequence comprising: an initial phase of aerobic treatment; after the initial phase of aerobic treatment, subjecting the water in the SBMBBR to at least one aerobic/anoxic cycle comprising: an aerobic treatment phase that maintains an ammonium ion concentration in the water greater than a threshold concentration; and a phase in which the biofilm carriers are maintained, at least locally, under anoxic conditions with this phase occurring in the aerobic treatment phase or after the aerobic treatment phase; and wherein the threshold concentration of ammonium ions is set to allow the development of anammox microorganisms during the phase in which the biofilm carriers are maintained, at least locally, under anoxic conditions.
10. The method of claim 9 wherein the method gives rise to DPAOs and wherein the method includes utilizing the DPAOs to accumulate polyphosphates in the water being treated.
11. The method of claim 10 wherein the method is performed without pre-seeding the water with anammox or DPAO microorganisms.
12. The method of claim 11 wherein the method is carried out without any addition of an external source of carbon or an external source of metal salts.
13. The method of claim 9 wherein the threshold of ammonium ion concentration is set at 1 mg N/L or higher.
14. The method of claim 9 wherein during the phase in which the biofilm carriers are maintained, at least locally, under anoxic conditions, the anammox and DPAO microorganisms transforms NH.sub.4.sup.+NO.sub.2.sup.− and NO.sub.3.sup.− into nitrogen without requiring an external source of carbon and at the same time the DPAOs also remove phosphorus from the water by accumulation.
15. The method of claim 9 wherein in each treatment sequence, the SBMBBR has a volume exchange ratio (ERV) between 90% and 100%.
16. The method of claim 9 wherein for each biological treatment cycle, the anaerobic treatment phase lasts from 30 minutes to 5 hours and at least one aerobic/anoxic cycle lasts from 1 hour to 10 hours.
17. The method of claim 9 wherein said biofilm carriers include a particular geometry that is configured to cause the biofilm carriers to remain in close proximity to each other during aeration in the SBMBBR so as to form local anoxic conditions during the aerobic treatment phase.
Description
LIST OF FIGURES
[0049] The invention, as well as its various advantages, will be more readily understood with the following description of two non-restrictive embodiments thereof, as well as one embodiment of a conventional method that is not part of the invention, with reference to the following figures:
[0050]
[0051]
[0052]
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[0055]
DESCRIPTION OF DETAILED EMBODIMENTS OF THE INVENTION
[0056] Tests were carried out according to two embodiments of the invention and compared to the results obtained by another test implementing the “conventional” method in a SBMBBR that is not part of the invention.
[0057] Test 6.1-Conventional implementation of the “SBMBBR” used for comparison purposes and not being part of the invention.
[0058] For this implementation, “conventional” carriers were used, such as “K5” carriers from Anoxkaldnes™. These carriers are perfectly fluidised when the aeration required to achieve aerobic conditions is applied.
[0059] The “conventional” SBR cycles consists of two phases: an anaerobic phase followed by an aerobic phase.
[0060] The carriers are not seeded with Anammox bacteria before the start of the tests.
[0061] Their oxygen content in the reaction medium during the aerobic phase are maintained at values comprised between 4 and 5 mg O.sub.2/L.
[0062] With reference to
[0063] With reference to
[0064] Test 6.2-Implementation of a method according to the invention with the introduction of an anoxic phase posterior to the aerobic phase.
[0065] For this implementation, “conventional” carriers were used, such as “K5” carriers from Anoxkaldnes™. These carriers are perfectly fluidised when the aeration required to achieve aerobic conditions is applied.
[0066] The carriers were not seeded with Anammox bacteria before the start of the tests. Until day 350, the SBMBBR operates in a conventional manner, with treatment cycles alternating between a 2-hour anaerobic phase and a 6-hour aerobic phase. This period corresponds to a seeding of the biofilm with dephosphating and nitrifying bacteria.
[0067] From day 350, an anoxic phase is added after the aerobic phase. Typically, the duration of the different operating phases is 2 to 3 hours for the anaerobic phase, 4 to 5 hours for the aerobic phase, and 1 to 2 hours for the anoxic phase. The aeration conditions (duration and oxygen content) of the aerobic phase are adjusted to reach an ammonia (NH.sub.4.sup.+) content in the reaction medium greater than or equal to 1 mg N/L before the anoxic phase. The oxygen content in the reaction medium is comprised between 4 and 5 mg O.sub.2/L for the aerobic phase, and 0 mg O.sub.2/L for the anoxic phase.
[0068] With reference to
[0069] With reference to
[0070] Before day 350 and until the implementation of the invention, the number of Anammox bacteria remains low, in the order of 10.sup.8 per m.sup.2 of carrier corresponding to the quantification limit of the analytical method.
[0071] After implementing the invention by adding an anoxic phase posterior to the aerobic phase, where the aeration conditions are adjusted to reach an ammonium ion (NH.sub.4.sup.+) content of more than 1 mg N/L, the number of Anammox bacteria increases progressively to reach 10.sup.11 Anammox bacteria/m.sup.2 of carrier. This number of bacteria is considered high and representative of proven Anammox activity in the biofilm.
[0072] With reference to
[0073] It has therefore been shown that the embodiment with an anoxic phase posterior to the aeration phase is more effective in removing nitrogen than the conventional method. Indeed, after the implementation of the “anoxic” strategy around day 350, the nitrogen removal efficiencies (soluble NGL) increased rapidly and stabilised at 75-80% over more than 200 days (day 450 to day 650). The soluble NGL content at the output of the reactor decreased significantly to less than 15 mg N/L over the same period. Before the implementation of the “anoxic” strategy, the measurements of Anammox bacteria by qPCR did not allow the detection of Anammox bacteria (quantities below the quantification limit in the order of 5.10.sup.8). From the implementation of the “anoxic” strategy around day 350, the quantities increased rapidly and significantly to reach values in the order of 1.10.sup.11. The development and activity of Anammox bacteria largely explain the good nitrogen removal efficiencies.
[0074] 6.3-Implementation of a method according to the invention where the creation of anoxic zones is concomitant with the aerobic phase.
[0075] For this implementation, “corrugated” carriers were used, such as “Z” carriers from Anoxkaldnes™. These carriers favour the creation of local anoxic zones during the aeration phases.
[0076] The implemented operation consists of a 2-hour anaerobic phase followed by a 6-hour aerobic phase. The dissolved oxygen content during the aerobic phase is comprised between 4 and 5 mg O.sub.2/L.
[0077] The “Z” carriers used, due to their geometry, can remain in close proximity to each other, thus forming local anoxic conditions during the aerobic treatment phase.
[0078] With reference to
[0079] With reference to
[0080] With reference to
[0081] With reference to