CA1057430A - Apparatus and process for removing ammonia nitrogen from waste water - Google Patents
Apparatus and process for removing ammonia nitrogen from waste waterInfo
- Publication number
- CA1057430A CA1057430A CA231,116A CA231116A CA1057430A CA 1057430 A CA1057430 A CA 1057430A CA 231116 A CA231116 A CA 231116A CA 1057430 A CA1057430 A CA 1057430A
- Authority
- CA
- Canada
- Prior art keywords
- waste water
- fluidized bed
- ammonia nitrogen
- cellular material
- nitrogen
- 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
Links
- 239000002351 wastewater Substances 0.000 title claims abstract description 110
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title abstract description 58
- 230000008569 process Effects 0.000 title abstract description 55
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000001301 oxygen Substances 0.000 claims abstract description 40
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 40
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 39
- 239000000463 material Substances 0.000 claims abstract description 32
- 230000001413 cellular effect Effects 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 20
- 230000031018 biological processes and functions Effects 0.000 claims abstract description 18
- 244000005700 microbiome Species 0.000 claims abstract description 17
- 239000007787 solid Substances 0.000 claims abstract description 15
- 239000002245 particle Substances 0.000 claims description 68
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 45
- 229910021529 ammonia Inorganic materials 0.000 claims description 19
- 230000005484 gravity Effects 0.000 claims description 14
- 241000894006 Bacteria Species 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000004576 sand Substances 0.000 claims description 4
- 238000000926 separation method Methods 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 239000011324 bead Substances 0.000 claims description 3
- 239000003818 cinder Substances 0.000 claims description 3
- 239000003245 coal Substances 0.000 claims description 3
- 239000002223 garnet Substances 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 238000004064 recycling Methods 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 2
- 229960000510 ammonia Drugs 0.000 claims 1
- 238000004891 communication Methods 0.000 claims 1
- 238000005086 pumping Methods 0.000 claims 1
- 230000012010 growth Effects 0.000 description 26
- 238000011282 treatment Methods 0.000 description 22
- 239000002699 waste material Substances 0.000 description 17
- 229960005419 nitrogen Drugs 0.000 description 11
- 230000001580 bacterial effect Effects 0.000 description 8
- 238000005299 abrasion Methods 0.000 description 6
- 241000902900 cellular organisms Species 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000009434 installation Methods 0.000 description 6
- 238000010899 nucleation Methods 0.000 description 6
- 238000001179 sorption measurement Methods 0.000 description 6
- 229910002651 NO3 Inorganic materials 0.000 description 5
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000005273 aeration Methods 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 230000001276 controlling effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 239000010802 sludge Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000003911 water pollution Methods 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000010865 sewage Substances 0.000 description 3
- 239000003643 water by type Substances 0.000 description 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000011001 backwashing Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000005243 fluidization Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000010808 liquid waste Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000010841 municipal wastewater Substances 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- 125000001477 organic nitrogen group Chemical group 0.000 description 2
- -1 oxy- Chemical class 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241000605159 Nitrobacter Species 0.000 description 1
- 241000605122 Nitrosomonas Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920005372 Plexiglas® Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 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 1
- 230000009471 action Effects 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 239000012237 artificial material Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000010170 biological method Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000001706 oxygenating effect Effects 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/02—Aerobic processes
- C02F3/12—Activated sludge processes
- C02F3/1205—Particular type of activated sludge processes
- C02F3/1215—Combinations of activated sludge treatment with precipitation, flocculation, coagulation and separation of phosphates
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/02—Aerobic processes
- C02F3/12—Activated sludge processes
- C02F3/26—Activated sludge processes using pure oxygen or oxygen-rich gas
-
- Y—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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biodiversity & Conservation Biology (AREA)
- Microbiology (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Biological Treatment Of Waste Water (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A biological process for removing ammonia nitrogen from waste water by forming a fluidized bed of microorganisms attached to a solid particulate carrier, continuously passing waste water to be treated through said fluidized bed, adding oxygen to said fluidized bed, retaining the waste water in the fluidized bed for a sufficient period of time while controlling other necessary parameters to biologically convert substantially all of the ammonia nitrogen to be removed from the waste water to oxidized forms of nitrogen, water and cellular material, and thence withdrawing the biologically converted products from the fluidized bed.
In another form of the invention apparatus is provided for effecting the foregoing process.
A biological process for removing ammonia nitrogen from waste water by forming a fluidized bed of microorganisms attached to a solid particulate carrier, continuously passing waste water to be treated through said fluidized bed, adding oxygen to said fluidized bed, retaining the waste water in the fluidized bed for a sufficient period of time while controlling other necessary parameters to biologically convert substantially all of the ammonia nitrogen to be removed from the waste water to oxidized forms of nitrogen, water and cellular material, and thence withdrawing the biologically converted products from the fluidized bed.
In another form of the invention apparatus is provided for effecting the foregoing process.
Description
~S743~11 ` .
,. , ".
BACKGROUND OF T~E INVENTION
The inven~ion relates to apparatus and , ' ~
process for the biological treatment of liquid wastes employing fluidi~ed beds. In particular, i~ is directed to a process for xemoving ammonia nitrogen from waste watex.
~, Untreated municipal wastes generally contain .
from 2~ to 50 milligrams of ni~rogen per liter, mostly in the form of ammoni5a and organic nitrogen. ~he serious . j - - .
i detrimental environmental effects of these compounds had not , been fully realized until the last decade. With the large amounts o~ fixed nitrogen in the form of ammonia `
' and other compounds that are being introduced into the - i i. I ;- ~. . -biosphere by the large scale use of synthetic fertilizers, ~- -' and with the demands man makes on his environment owing -to population congestion, there definitely appears to be ; an imbalance developing in our ecological system that may have long range consequences for future generations. The -~
presence of such nutrients in natural waters causes ~ ~
fertilization and vegetative growth in the form of algal ;
~ blooms. Such blooms often result in accelerated eutro~hicat-! ion.
Conventional methods of municipal sewase i treatment, chiefly activatcd sludge and trickling ;, .
i filtration are designed to remove solids and oxygen demand~
ing organic material from the waste water. During ~hese .,: ' ~ .
'. ' ~ ~;'; -.
~. '' . , -:: : : : : - : , ., i treatment processes some of the organic nitrogen is converted into the ammonia form. Chemical and physical 'methods such as chlorination and ion exchange have been tried in small scale e-xperime-nts to remove these ammonia compounds from the waste water, but costs have been too prohibitive to attempt these methods of treatment in large scale installations. Although ammonia stripping is economically feasible, it suffers the disadvantages of poor operation or shutdown in winter and the introduction of ammonia into the atmosphere.
Biological methods of treatment have been .; ji ' ~
most frequently used to remove ,ammonia in typical large installations. Oxidation of ammonia nitrogen to nitrate I~nitrogen can be accomplished in an activated sludge ~ -` treatment plant by increasing aeration time in the plant ~from 3 - 6 hours to 10 or more hours. This requires the use of large aeration basins and is often inefficient ~
because of difficulties in controlling the system. This ~ ;
oxidation of ammonia to nitrate, termed nitrification, can also be accomplished by aerating the effluent from the activated sludge treatment process in a separate aeration basin. This facilitates control of the nitrification I~
, process but requires additional aeration basins with an additional aeration time of 3 to 6 hours.
. :
Certain experimental nitrification processes have employed the use of up-flow columns or beds. Such ` ~ packed beds tend to become clogged as solids in the waste water are filtered out and further as attached biota undergo uncontrolled yrowth on the stone media. Such -; . , .. . . . .
., .
~ ` _3_ . . : :
.. . . . .
, ~OS~430 blockage causes insurmountable head losses. These losses ~.
must ~e relieved by frequent and impractical back washing of the bed. Also, detention times in excess of one hour are required.
An example of a prior art system.is described Il in the publication by, St. Amant, P.P. and ilcCarty, P.L. :.
¦¦ "Treatment of High Nitrate Waters", JOURNAL OF AMERICAN
WATER WORKS ASSOCIATION, pp. 6~.9-66:9, 1.969. This ¦ .
publication is concerned with an up-flow denitrificaticn I :
system, which is basically a packed bed of one inch stone, `~
as compared to the present application which is concerned .. with a ~uidized bed of small particles. Hence, the operating ..
s parameters and results are completely different. Another ` . ¦ example of a prior ar~ system is described in the publication .: ~ :
'~ ~ by, Weber, W.J. Jr. and Morris, J.C. "Kinetics of Adsorption in Columns of Fluidized Media", JOURNAL OF ~MERICAN
i WATER WORKS ASSOCIATION, pp. 425,430, 443, 1965. This publi~
' 1 cation teaches the use of an expanded bed c~lumn for a . l physical ad~orption process, i.e, the adsorption of .:~ . organic carbon by porous adsorbent activated . `~ -: ' carbon particles. The process of Weber et al does not ~:.
. . rely upon the use of biological action, as is the case in the :. ; present application. . . ~ -Still another example of prior art systems ;- ~.
~ is the Savage Patent No~ 3,709,364 issued in January `. 1973. The process described in this patent is essentially ~ a'deep bed filter'r which employs a down-flow system.::
:~l ; With this type of system, as the spaces between the .~. . particles.become plugged.with solid.wastes, great.head . .
."' , ~
~4~
'''' ~ '' ' ' ' . ' ~' . ' ' ~.' ' j ~L[)57~L3~ .
. :
.: .
; losses result. Savage recognized this problem and provided means for intermittent back- washing to agitate this filter media and remove suspended solids collected on it. Thus, the Savage system was predicated on different ; principles and employed different parameters as compared to the present application.
,Other related patents and publications in this art include the following~
:~ .
~ United States Patents ,,.: - .
No. 2,676,919 M. Pirnie April, 1954 ` l No. Re 24, 219 M. Pirnie September, 1956 No. 2,834,466 L. Hament May, 1958 No. 2,992,986 W.T. Ingram July, 1961 No. 3,075,828 Tsuneo Kato et al. January, 1963 :, l; , ~ .
- No. 3,173,862 J.S. Clements et al.March, 1965 No. 3,219,577 T.J. Powers November, 1965 No. 3,424,674 P.J. Webber January, 1966 ~.
No. 3,23~,434 W. Albersmeyer Pebruary, 1966 No. 3,371,033 E.D. Simmons et al February, 1968 No. 3,401,113 R.D.Pruessner et al September, 1968 No. 3,543,937 J.M. Choun December, 1970 No. 3,547,816 Horiguchi et al. December, 1970 , , : .
~ ~ Publications ~ ~ :- . .
- Weber, W.J., Jr., Hopkins, C.B. and Bloom, R.Jr., Physiochemical Treatment of Waste Water", Journal Water Pollution Control Federation, Vol. 42, pp.83-89, (1969).
'; ~
.~ . . ~.
:' ' :
~5~
.:
.. . . . . ..
,........ .. ..
Tamblyn, T.A. and Sword, Bryan R., "The Anaerobic Filter for the Denitrification of Agricultural Subsurface Drainage" Paper presented at 24th Annual Purdue Industrial Waste Conference, Lafayette, Indiana on May 7, 1969~ -Beer, Carl, "Evaluation of Anaerobic Denitrification and Processes", Proc. Paper 7211, Seidel, D.F. and Crites, R.W., Ed., (April, 1970).
Castaldi, F. and Jeris, J.S., "Still Wanted: Economical Controlled Denitrification", Water and Wastes En~ineering Vol. 41, 36-38, (June 1971).
.: .
Beer, C., Jeris, J.S. and Mueller, J.A. "Biological Denitrification of Effluents in a Fludiized Granular Bed, Phase I" prepared for New York State Department of ~ `
Environment Conservation, published Manhattan College;
(March 1972).
.
- Weber, W.J., Jr., and Morris, J.C. "Kinetics of Adsorption ~
` in Columns of Fluidized Media" Journal of American ~- -Water Works Association, pp. 425,430, Vol. 443 (1965).
St. Amant, P.P. and McCartyj P.L., "Treatment of High ~' Nitrate Waters", Journal of American Water Works Association pp. 659-662 (1969). ' ;
.. ~ "
McCarty, Perry L. and Haug, Roger T., "Nitrification l with submerged Filters" Journal Water Pollution Con-`~, trol Federation , Vol. 44, No. 11 (~lovember 197~).
;~ j McCarty, Perry L. and Young, James C., "The Anaerobic ; Filter for Waste Treatment", Journa Water Pollution Control Federation, VolO 41, R 160 (1969).
. ' " ~ . .
Weber, W.J., Jr., Friedman, L.D. and Bloom, R.Jr., ~;
"Biologically - Extended Physicochemical Treatment", ~ -Paper presented at 6th International Water Pollution '~ ~ Control Conference at the University of Michigan on June 22, 1972.
' . ~
This article discloses an adsorption process and therefore a porous substrate is necessary, i.e. sand and the l~ke material cannot be employed. There is no build-up of .51udge disclosed and stoichiometric amounts of oxygen are not employed.
:~` ':
: '~
.' ' . - - . . ~ - -. , . :
. ~ . , , - . - .
~5~3~) ~
Accordingly, while the art has recognized the desirability of employing biological organisms to remove ammonia from waste water, it has not succeeded in ,:
providing an inexpensive and highly efficient process for rapidly treating large quantities of waste water.
~ Accordingly, there exists a critical need for a process -~ free of the defects and deficiencies of the prior art to purify waste water.
SUMMARY OF THE INVENTION
.
; Ii is, therefore, a primary object of the invention to provide a relatively inexpensive process , employing biological organisms for oxidizing the ammonia nitrogen content of waste waters to oxidized forms of nitrogen.
As employed in this application the term ~ ;~
~, "waste water" or "liquid waste" includes organic or ; ~
inorganic liquids or mixtures thereof containing biologi- -~` , cally decomposable contaminants and containing the equiva- ;
. :-lent of at least about 10 milligrams per liter of nitrogen , in a reduced form; particularly the ammonia form. Most municipal waste waters and industrial waste waters of equivalent strength fall within the above definition of waste water.
It is another object of the invention to ' reduce the ammonia nitrogen content of waste water -~
'~ employing a fluidized bed of biological organisms and ~ simultaneously controlling the tendency of the bed i ~ i particles to become excessively enlarged by excess biological growth.
It is an additional object to treat waste . ' ' ' : : ' ':
-7~
,.~.,., ., . .. , : , ~0574~30 , water containing significant amounts of suspended solids without effectively reducing the efficiency of the process.
A further object of the invention is to provide an efficient waste treatment process adapted to operate at lower detention times compared to traditional , ~ processes.
The aforementioned and other objects are met in a process for removing ammonia nitrogen from ~ ' waste water by generating a fluidized bed from waste ; ; water and biota,adapted to oxidize ammonia nitrogen by ~' ` use of aerobic biota attached to a solid particulate ~, carrier adapted to be fluidized; then metering sufficient .. . . .
~ ~ amounts of oxygen into the bed to allow the biota to ','~, oxidize the ammonia nitrogen content of the waste water ', ~ passing therethrough and thereafter removing excess bacterial growth formed on said carrier during the pro~
, cess.
~ The term "fluidized bed" as employed herein ~ -`i refers to the flow of a suitable liquid upwardly through ~' 1. ' , .
a bed of suitable sized particles at a velocity sufficiently ~, ' ' high to buoy the particles, to OvercQme the influence ' ,~
,~ of gravity, and to impart to ~hem an appearance of ' , movement within the bed; said bed being expanded to a '", greater depth than when no flow is passing therethrough. '~' The particles travel to different parts of the bed and are imparted with movement within the bed. On the con- ;
l , trary, in an expanded bed as employed in the prior art ,~ systems such as the systems mentioned hereinbefore in '~' .,~
~', connection with the two Weber et al publications and the ', Huether Patent No. 3,658,697, the particles are primarily `'1 substantiallY suspended in a ~iven volume by the water passing therethrough.
~f~ As waste water containing nitrogen in the :, , ~ 8 form of ammonia is passed through the fluidized bed, bacterial growth on the particle~s is accelerated and the bed particle size increases. If unchecked, the bed particles become enlarged and may agglomerate, thus reducing the biological surface area per unit folume of the reactor and the efficiency of the column. Further, the particles tend to be reduced in specific gravity as they enlarge and/or agglomerate and tend to be carried away from the bed. It is a feature of the present process that the excess cellular material or bacterial growth formed on the particles during the process is mechanically removed thereby overcoming the tendency of the particles I ~ ¦
to be carried away in the process effluent. Accordingly, ¦
the term "excess cellular material" as employed herein refers to the excess of such material attached to the particulate carrier beyond that needed for the normal operation of the system.
Employing a fluidized bed for biological treat-ment al~o p~rmits waste water containing substantial amounts of suspended matter to be treated. Such suspended matter readily passes through the fluidized bed. Other types of beds, such as packed beds, are subject to plug-ging and excess pressure losses caused by excess growth and by retention of suspended particulate matter contained i ;
in waste water.
Another substantial advantage of the present fluidized bed process is the unexpected high flow rates and removal efficiencies achieved by the fluidized system.
The process is readily adapted to meet the water and waste water purification needs of municipalities and industry.
~'', , I ' l -9 ll ~L05~30 1 ~
In view of the foregoing r this invention contem-I , plates a new and improved biological process for removing `
; 1 amm,onia nitrogen from waste water which includes i the steps of forming a fluidized bed of microorganisms - 1l attached to a solid particulate carrier, continuously passing waste water to be treated through the fluidized , I bed, adding oxygen to the fluidized bed, and retaining ! the waste water in ~he fluidized bed for a sufficient . j . .. . ............................... .
period of time, while maintaining the fluidized bed at a sufficient temperature, and while maintaining the fluidized bed under aerobic conditions to biologically .. ~ ~, I .
convert substantially all of the ammonia nitrogen to be `I removed from the waste water to oxidized forms of nitrogen, `~including nitrite and/or nitrate nitrogen, water, and j1 cellular material. The process further comprises the ~,steps of continuously withdrawing the oxidized forms of nitrogen and water from the fluidized bed, and removing excess cellular material from the particulate carrier. In ;
il another form of the inVentiQn, apparatus is provided to ; ~ effect the foregoing process.
... ,1 1 . :.
j BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a flow sheet illustrative of the process of the invention with the various processing :.
components shown more or less diagrammatically, and Fig. 2 is a flow sheet illustrative of the process of 1 a second embodiment of the invention.
.. . .
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~l .
. ~ , ., , : . , ~057430 I D~SCRIPTION OF Tll~ PREFERR~D EMBODIMENTS
,j _ I
While applicable to the treatment of any fluid containing ammonia-nitrogen to which bacteria can become acclimated, the present process is most readily adapted for nitrification at secondary waste water treatment faci-1 lities. Designed for complete nitrification of wastewater, the process may also be installed at overloaded conventional trickling filtration plants or activated sludge processing facilities where BOD is being removed ; but where nitrification becomes necessary particularly ; where land availability is limited. It has far-reaching . !
capabilities to augment overloaded treatment systems.
~ Ij For most practical applications, the waste water ¦ I to be treated will contain at least the equivalent of about ;
~' ' 10 milligrams per liter of ammonia nitrogen. Of course, j , the process is able to treat waste water containing less than this amount. I
There must be sufficient oxygen in the feed waste water in order to provide the stoichiometric amount for oxidation of the ammonia to be removed. Pure oxygen or ani , oxygen cor.taining gas, such as air, may be injected into . ~j . . .
the feed preferably prior to entry of the feed into the fluidized bed. If desired, the oxygen may be injected into ~ ;~
-~ the fluidized bed or both into the feed and bed To ~ ~ ~
increase the efficiency of the oxygen transfer, the ; ~ ~1 effluent gases from the fluidized bed can be recycled into the waste water, or the waste water may be recycled to enhance greater oxygen adsorption.
By way of an example of the process, waste ~, water is passed through the up-flow fluidized bed accor-~ .
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; ding to the invention in the presence of appropriate ;:, li ; .
microorganisms which convert am~Zonia nitrogen to oxidized forms of nitrogen, including nitrite and/or nitrate nitro-gen and cellular material. A general equation for the biological phenomenon may be expressed as follows:
C2 + NH3 ~ 2 + Microorganisms-~ N02 and/or NO
H20 ~ Microorganisms Sufficient oxygen must be present to satisfy this stoichiometric minimum in light of the amounts of ammonia `
present in the waste water. Generally, from about 3.0 to about 5.0 milligrams of dissolved oxygen are needed for each milligram of ammonia oxidized. Lesser amounts can be ~ 1 employed; however, the process generally becomes less efficient. If greater amounts are employed, then an excess of oxygen is provided which is unnecessary to the ~;
implementation of the process. In certain instances it will not be possible to accurately determine the ammonia nitrogen in the waste water. Therefore, as a practical measure it is preferable to saturate the waste water as far as practicable with dissolved oxygen. The solubility of pure oxygen is about 40 milligrams per liter at room temperature at atmospheric conditions. I -In order to provide dissolved oxygen in amounts approaching the solubility of pure oxygen it has been found that a fermentor turbine can be efficiently employed. The fermentor turbine has a hollow annular shaft with blades or turbines at the base of the shaft.
Waste wateris passed through a tank into which the fermentor turbine is disposed. Oxygen is passed through the central orifice of the turbine and is broken up into a plurality : ~... . ., ~ .
. :: , .
, ' ' ::
5~436) of tiny bubblcs by ~he spinning blades at the base of the turbine shaft. Other gas transfer devices known in the -art may also be used.
A fluidized bed system is preferably generated by passing ~aste water through an upright column containing microorganisms attached to a particulate carrier or sub-¦ strate. In general, the carriers will be seeded withbacteria from aerobic processes adapted to feed on waste water. Nitrosomonas and nitrobacter, which are naturally found in municipal waste water are particularly I preferred for this purpose.
¦ Suitable carrier material~ for the biota or microorganisms include natural or artificial materials such as coal, volcanic cinders, glass or plastic beads, ~1 sand, alumina, garnet and activated carbon particles. The ~
:!
¦ size of the particles chosen is a function of both specific 1I gravity and surface area. For the most part, the carrier particles are between about 0.2 and about 3 millimeters 1 in diameter. Employing the preferred flow rates of the l ~
¦~ present invention, enhanced results are obtained by bed ,3 :
¦! particles having a diameter of from about 0.4 to about 1.5 millimeters. The above discussion assumes the presence !
of spherical particles, but the particles in most cases would not be spherical. Most preferably, the particles are of a uniform size. While the aforesaid bed carriar materials are illustrative of the preferred substrates, nonetheless other materials, nontoxic to the bacteria, whether natural or synthetic, can be employed.
It has keen found that substantial amounts of ammonia ~3 can be aerobically nitrified in a fraction of bed, sometimes -: in the first few feet adjacent the influent feed. Accordingly, it may be sufficient to provide aerobic conditions for only a fraction of the bed height. 5imilar results are obtained for aerobic removal of B~D. Further, it is within the scope of the invention to carry out the process in this manner.
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; For enhanced ammonia removal, the bed particles preferably have a thin layer of bacteria seeded thereon.
Preferably, the bed particles are first cultured with seed bacteria such as those present in sewage. Seeding is ' provided externally, or yreferably, internally within the ; " .
fluidized bed column. For this purpose the carrier parti-cles are introduced into the column and thereafter waste water which is to be trea~ed is fed through the column. It has been found that seeding is enhanced by recycling all - .
;
or a portion of the flow, controlling the pN and con-< I centrations of NH3 and alkalinity. Seed bacteria or bacteria naturally present in the sewage rapidly grow around the bed particles and become acclimated to the system~ The specific gravity of the seeded particles s I is preferably no less than 1.1 and preferably at least about 1.2 in order to insure that such particles are not carried out of the system during operation of the fluidized , ;I bed. I ;
-` " By way of an example of the operation, waste water, appropriately oxygenated if necessary, enters a l vertical cylindrical column through a distribution manifold , in the column base. A suitable distribution manifold i has a series of spaced apart inlet ports which regulate the flow of waste water through the column. Obviously, a wide assortment of conventional distribution manifold 'I , :
systems could be utilized also.
The pressure of the waste water influent at the point of fluidization varies depending on many factors, including the quantity of bed particles, their specific gravity and the degree of pressurization set in the column~
.i, , ; .
' i , , . I
~05743(~ 1 For the vertical column fluidized bed systems, the oxygen-ated feed is pumped into the column at a rate sufficient 'I
to support the seeded particles in the state of fluidiza-tion as hereinbefore described.
Where waste water contains highly concentrated wastes, microorganisms or occluded solids, it may be desirable to inject the oxygen at greater than atmospheric pressure. At increased pressures larger amounts of oxy-, gen are dissolved in the waste water to satisfy the increasedstoichiometric requirements. For example, amounts as great , ,l as about 150 milligrams of oxygen per liter of waste water , and more can be supplied to the feed at super atmospheric pressure. ~ ;~
In general the flow rate into the col~mn is ~J ¦~ sufficient to provide a fluidized bed according to the invention. Depending upon the size and specific gravity of ~-the bed particles, among other factors, the flow rate ,' is usually at least about 6 gallons per minute per square foot of bed. By adjusting the specific gravity of the ,' bed particles, by employing denser bed particles and !
ii~ the like, the process can be carried out at very high .1 ' ,1 flow rates, possibly even the order of hundreds of gallons per minute per square foot of bed. Commercially, it is desirable to operate at flow rates approaching 100 gallons per minute per square foot of bed. Fluidized beds operating according to the fundamental principles of the present invention have been successfully operated at flow rates of about 25 gallons per minuke per square foot of bed and operations at higher rates are well within present technology as set ~orth herein.
: . .
It has been found that enhanced results are .~ :
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~L0579L3~ ;
obtained, and accordingly, it is preferred to provide a flow rate into the column from about 6 to about 40 gallons per minute per square foot of natural or artificial bed.
Further enhanced results are obtained when the flow rate is from about 8 to about 25 gallons per minute per square foot of bed. Depending upon the specific flow rate selected, the actual dwell time within the column for a volume of waste water can be as little as from about 2 to about 5 minutes. In general, the dwell time within the column is usually under about 30 minutes and most fre-quently less than about 15 minutes per up to about 12 feet of bed height, but the actual dwell time is a function of the size of the reactor. The flow rate iæ preferably adjusted to compensate for the size and specific gravity of the seed particles.
For a given bed, as the flow rate is incre~sed ;~ in order to increase the volume of waste water being `~3 ; treated, the specific bed of microorganism attached ~ particles will increase in height. In order to compensate .
for the tendency of the bed to increase in height at higher : . ~
flow rates, it is desirable to employ additional bed particles or to employ bed particles of higher specific ` gravity.
As the waste water is pumped into the column an area immediately above the distribution manifold may be ;l free of seeded particles although bed particles with sufficient growth may remain. This phenomenon has also been observed during initial seeding periods of the bed but disappeared as seeding of the carrier particles progressed.
' This interface height, then ~the height from the distri-bution manifold to the bottom of the seeded fluidized bed in a vertical column) is a function of the flow rate of the column, the temperature, the specific gravity of the bed particles and the length of time of the seeding ` ' ' - /~' :
......
period as ~ell as the nature of the distribution manifold. I
Practically, this phenomenon has a minimal effect, if any, on the column's efficiency. Generally as flow rate increases interface height increases and conversely as flow rate decreases interface height decreases.
In general~ the pH of the fluidized system will not require external manipulation. If need be, it may be adjusted to fall within the range of from about 5.5 to 9.5. Best results are obtained at a pH from about 6.0 to 9Ø The internal temperature of the fluidized column should be sufficient to permit bacterial activity. For this purpose the bed temperature is from about 5 to about 45 C. The bed temperature will vary with that of the influent waste water and, accordingly, ambient operating temperatures on the order of from about 8 to about 30 C. will be the nominal bed temperatures and are entirely satisfactory.
As the ammonia oxidation reaction proceeds in the fluidized bed, bacteria tend to grow on the surface !
;~ oE the carrier particles. After a time, if unchec~ed, bed particles tend to form thick layers and expand to the extent that they form agglomerates, and/or gelatinous masses. I 1 Should this be permitted to occur, then the surface area -' `~ per unit reactor volume available for biological reaction is great . ~ .
ly reduced and the efficiency of the process is correspondingly reduced. Further, particles tend to be carried out of the fluidized bed as their specific gravity decreases. They aldo tend to entrap or become attached to gas bubbles, such as ,: . . .... . .~:, , ~ , 1057~3(~
oxygen bubble~ from the injected source. The gas bubbles reduce the specific gravity of the particles and tend to carry them away from the bed toward the top of the column where they can collect as an undesirable floc and/or leave the system.
In order to overcome these problems excess bacterial growth is preferably mechanically removed from the particles although chemical and biological means or combinations thereof may be employed to supplement mechani-cal removal. Sufficient growth in the form of a ~hin layer of bacteria must remain on the particles in order to .i , .
` preserve the efficiency of the process. Removing all growth ~, which has been suggested in the prior art for up-flow ` expanded bed process used for treating waste water to re-move carbon by adsorption, des~roys the efficiency of the . ,, present process. In one embodiment, growth is regulated by removing predetermined quantities of bed particles from the column by a valve-controlled outlet port and mechani-cally ~gitating and abrading the particles. Thls operation may be performed in a separate abrasion vessel employing a mixer which resemh-les the rotating knife in a Waring Blender.
The abraded particles are ~hen returned to the bottom of the fluidized bed. Alternately, the particles in ~he abrasion vessel are subjected to the action of compressed air or water sprays to remove excess microorganisms. Other suitable agitation mechanisms and apparatus wiil be apparent to those skilled in the art. After treatment, the abraded particles are metered into the fluidized bed at its base by a suitable inlet port. The withdrawal of measured amounts of bed particles, their cleaning and recyling into :
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Il ~057gL30 . . .
the process can be accomplished without a significant ,1 interference with the continuity of the process.
., , By way of example, in a second embodiment, bed particles are allowed to be carried out in the effluent i from the column into a set-tling tank ~rom which they are pumped into the bottom of the column. Separation of the ~j excess cellular material growth fr,om ~h,_ par~ti,_ulate~carrier ;¦ is effected by the pump. Fig. 1 illustrates this process.
Waste water and air or oxygen is introduced into a flui~
dized bsd column 10 through an inlet port 11 for treatment therein. The treated waste water containing bed particles is ~ :~
¦ exhaus~ed as at 12 from the fluidized bed column 10 into a settling tank 14. Separation of the treated waste water or .!' ,¦ effluent 16 and bed particles 18 occurs in the settling tank.
The separated bed particles are-then pumped back into the j fluidized bed column as indicated at 20. Separation of the growth from the carrier particles occurs by abrasion in a pump 22. When the mixture of the abraded carrier and the ~` !
growth or excess cellular material is pumped back into the column 10, the carrier particles will remain in the column while the excess cellular material will be carrii~d on through the system to the effluent 16.
By way of example, in a third and more preferred ~-emkodiment, the particles are treated in situ in order to remove excess bacterial growth from their outer sur-faces. It has been found that excess bacterial growth is readily removed from floc, agglomerates ard/or bed particles at the top (or downstream side) of the bed, by a sharp rotating blade or flexible agitator. These mechanisms j l ' , ' ' 'j , j . :
- 19 ~
',' ~ :' ' 79~30 .
shear the bacteria from the carrier particle and thereby remove excess growth. The stirrer provides continuous control of the height of the fluidized bed. Other mechanical mixers, ultrasonic devices, bafle plates and other abrasion-type surfaces, or even water or compressed air jets directed upwardly and sidewardly against the column walls to create agitation vortices and the like, as well as other suitable conventional agitating means, can be employed within the column.
Where the bacteria are abraded batchwise to control growth, it has been found that sufficient growth is removed, when the height of the fluidized bed after treatment is reduced on the order of from about 10 to 25 percent of its original expanded length at the same flow rate. At highly elevated or substantially reduced flow rates, the height may be somewhat above or below the afore-said range. For removal of excess growth in situ using the .. .
i' air cleaning method, for example, the flow rate to the . ~ , .
column may be reduced to about 1/3 normal flow (reduction , is dependent on operating flow rate). The bed will settle to a new lower height. Air is injected into the bed to cause abrasion. During and immediately after this abrasion, the removed growth is carried out of the reactor and exhaus-ted from the system. Thereafter, the flow rate may be increased to its normal velocity.
Depending upon the nature of the waste water and the concentration of contaminants, it may prove useful to employ more than one column connectedin series. It has been found practical in many cases to employ the effluent from '' ' .
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105743~
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th~ first column as the influent feed for a second column.
Accordingly, a plural column system may provide enhanced results for treatment of industrial, municipal and other waste waters. In a two col~mn system, ammonia nitrogen is further oxidized by directing ~he effluent from the first co-lumn into the second column as the sole influent, or in combination with fresh sewage. During start-up of the column it has, in certain cases, been found useful to recycle at least a portion of the effluent treated to the column .; , .
in order to promote initial growth of bacteria on the bed carrier particles in situ.
. ! .
By way of example, Fig. 2 shows a somewhat preferred embodiment of the process according to the invention. Waste water is introduced through an inlet pipe 23, valve 24 and inlet port 25 into the Iower portion of cylindrical column 26 through a manifold 28 in the base of the column. Microorganism or biota-seeded bed particles are fluidized by the passage of waste watar thrsugh the column and form a fluidized bed 30. The interface height sf the fluidized bed is indicated at 32j forming a chamber 33 7 ' thereabsve in the column. Treated waste water or effluent is exhausted from the column after passage through the fluidized bed and chamber 33, as at 34. Then the effluent may be passed thrsugh an effluent purifier 35 such as a settling tank or for treatment with flocculants or the like, ~;;
if necessary. Selected portions of the effluent,as xequired, ;~
are recycled through pipe line 36, containing a pump 37, to the influent waste water inlet port 25. This serves the i~
following purposes: (13 to promote growth of the biota or ~
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~057~3~
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microorganisms on the particles during seeding operations;
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BACKGROUND OF T~E INVENTION
The inven~ion relates to apparatus and , ' ~
process for the biological treatment of liquid wastes employing fluidi~ed beds. In particular, i~ is directed to a process for xemoving ammonia nitrogen from waste watex.
~, Untreated municipal wastes generally contain .
from 2~ to 50 milligrams of ni~rogen per liter, mostly in the form of ammoni5a and organic nitrogen. ~he serious . j - - .
i detrimental environmental effects of these compounds had not , been fully realized until the last decade. With the large amounts o~ fixed nitrogen in the form of ammonia `
' and other compounds that are being introduced into the - i i. I ;- ~. . -biosphere by the large scale use of synthetic fertilizers, ~- -' and with the demands man makes on his environment owing -to population congestion, there definitely appears to be ; an imbalance developing in our ecological system that may have long range consequences for future generations. The -~
presence of such nutrients in natural waters causes ~ ~
fertilization and vegetative growth in the form of algal ;
~ blooms. Such blooms often result in accelerated eutro~hicat-! ion.
Conventional methods of municipal sewase i treatment, chiefly activatcd sludge and trickling ;, .
i filtration are designed to remove solids and oxygen demand~
ing organic material from the waste water. During ~hese .,: ' ~ .
'. ' ~ ~;'; -.
~. '' . , -:: : : : : - : , ., i treatment processes some of the organic nitrogen is converted into the ammonia form. Chemical and physical 'methods such as chlorination and ion exchange have been tried in small scale e-xperime-nts to remove these ammonia compounds from the waste water, but costs have been too prohibitive to attempt these methods of treatment in large scale installations. Although ammonia stripping is economically feasible, it suffers the disadvantages of poor operation or shutdown in winter and the introduction of ammonia into the atmosphere.
Biological methods of treatment have been .; ji ' ~
most frequently used to remove ,ammonia in typical large installations. Oxidation of ammonia nitrogen to nitrate I~nitrogen can be accomplished in an activated sludge ~ -` treatment plant by increasing aeration time in the plant ~from 3 - 6 hours to 10 or more hours. This requires the use of large aeration basins and is often inefficient ~
because of difficulties in controlling the system. This ~ ;
oxidation of ammonia to nitrate, termed nitrification, can also be accomplished by aerating the effluent from the activated sludge treatment process in a separate aeration basin. This facilitates control of the nitrification I~
, process but requires additional aeration basins with an additional aeration time of 3 to 6 hours.
. :
Certain experimental nitrification processes have employed the use of up-flow columns or beds. Such ` ~ packed beds tend to become clogged as solids in the waste water are filtered out and further as attached biota undergo uncontrolled yrowth on the stone media. Such -; . , .. . . . .
., .
~ ` _3_ . . : :
.. . . . .
, ~OS~430 blockage causes insurmountable head losses. These losses ~.
must ~e relieved by frequent and impractical back washing of the bed. Also, detention times in excess of one hour are required.
An example of a prior art system.is described Il in the publication by, St. Amant, P.P. and ilcCarty, P.L. :.
¦¦ "Treatment of High Nitrate Waters", JOURNAL OF AMERICAN
WATER WORKS ASSOCIATION, pp. 6~.9-66:9, 1.969. This ¦ .
publication is concerned with an up-flow denitrificaticn I :
system, which is basically a packed bed of one inch stone, `~
as compared to the present application which is concerned .. with a ~uidized bed of small particles. Hence, the operating ..
s parameters and results are completely different. Another ` . ¦ example of a prior ar~ system is described in the publication .: ~ :
'~ ~ by, Weber, W.J. Jr. and Morris, J.C. "Kinetics of Adsorption in Columns of Fluidized Media", JOURNAL OF ~MERICAN
i WATER WORKS ASSOCIATION, pp. 425,430, 443, 1965. This publi~
' 1 cation teaches the use of an expanded bed c~lumn for a . l physical ad~orption process, i.e, the adsorption of .:~ . organic carbon by porous adsorbent activated . `~ -: ' carbon particles. The process of Weber et al does not ~:.
. . rely upon the use of biological action, as is the case in the :. ; present application. . . ~ -Still another example of prior art systems ;- ~.
~ is the Savage Patent No~ 3,709,364 issued in January `. 1973. The process described in this patent is essentially ~ a'deep bed filter'r which employs a down-flow system.::
:~l ; With this type of system, as the spaces between the .~. . particles.become plugged.with solid.wastes, great.head . .
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; losses result. Savage recognized this problem and provided means for intermittent back- washing to agitate this filter media and remove suspended solids collected on it. Thus, the Savage system was predicated on different ; principles and employed different parameters as compared to the present application.
,Other related patents and publications in this art include the following~
:~ .
~ United States Patents ,,.: - .
No. 2,676,919 M. Pirnie April, 1954 ` l No. Re 24, 219 M. Pirnie September, 1956 No. 2,834,466 L. Hament May, 1958 No. 2,992,986 W.T. Ingram July, 1961 No. 3,075,828 Tsuneo Kato et al. January, 1963 :, l; , ~ .
- No. 3,173,862 J.S. Clements et al.March, 1965 No. 3,219,577 T.J. Powers November, 1965 No. 3,424,674 P.J. Webber January, 1966 ~.
No. 3,23~,434 W. Albersmeyer Pebruary, 1966 No. 3,371,033 E.D. Simmons et al February, 1968 No. 3,401,113 R.D.Pruessner et al September, 1968 No. 3,543,937 J.M. Choun December, 1970 No. 3,547,816 Horiguchi et al. December, 1970 , , : .
~ ~ Publications ~ ~ :- . .
- Weber, W.J., Jr., Hopkins, C.B. and Bloom, R.Jr., Physiochemical Treatment of Waste Water", Journal Water Pollution Control Federation, Vol. 42, pp.83-89, (1969).
'; ~
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.:
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Tamblyn, T.A. and Sword, Bryan R., "The Anaerobic Filter for the Denitrification of Agricultural Subsurface Drainage" Paper presented at 24th Annual Purdue Industrial Waste Conference, Lafayette, Indiana on May 7, 1969~ -Beer, Carl, "Evaluation of Anaerobic Denitrification and Processes", Proc. Paper 7211, Seidel, D.F. and Crites, R.W., Ed., (April, 1970).
Castaldi, F. and Jeris, J.S., "Still Wanted: Economical Controlled Denitrification", Water and Wastes En~ineering Vol. 41, 36-38, (June 1971).
.: .
Beer, C., Jeris, J.S. and Mueller, J.A. "Biological Denitrification of Effluents in a Fludiized Granular Bed, Phase I" prepared for New York State Department of ~ `
Environment Conservation, published Manhattan College;
(March 1972).
.
- Weber, W.J., Jr., and Morris, J.C. "Kinetics of Adsorption ~
` in Columns of Fluidized Media" Journal of American ~- -Water Works Association, pp. 425,430, Vol. 443 (1965).
St. Amant, P.P. and McCartyj P.L., "Treatment of High ~' Nitrate Waters", Journal of American Water Works Association pp. 659-662 (1969). ' ;
.. ~ "
McCarty, Perry L. and Haug, Roger T., "Nitrification l with submerged Filters" Journal Water Pollution Con-`~, trol Federation , Vol. 44, No. 11 (~lovember 197~).
;~ j McCarty, Perry L. and Young, James C., "The Anaerobic ; Filter for Waste Treatment", Journa Water Pollution Control Federation, VolO 41, R 160 (1969).
. ' " ~ . .
Weber, W.J., Jr., Friedman, L.D. and Bloom, R.Jr., ~;
"Biologically - Extended Physicochemical Treatment", ~ -Paper presented at 6th International Water Pollution '~ ~ Control Conference at the University of Michigan on June 22, 1972.
' . ~
This article discloses an adsorption process and therefore a porous substrate is necessary, i.e. sand and the l~ke material cannot be employed. There is no build-up of .51udge disclosed and stoichiometric amounts of oxygen are not employed.
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Accordingly, while the art has recognized the desirability of employing biological organisms to remove ammonia from waste water, it has not succeeded in ,:
providing an inexpensive and highly efficient process for rapidly treating large quantities of waste water.
~ Accordingly, there exists a critical need for a process -~ free of the defects and deficiencies of the prior art to purify waste water.
SUMMARY OF THE INVENTION
.
; Ii is, therefore, a primary object of the invention to provide a relatively inexpensive process , employing biological organisms for oxidizing the ammonia nitrogen content of waste waters to oxidized forms of nitrogen.
As employed in this application the term ~ ;~
~, "waste water" or "liquid waste" includes organic or ; ~
inorganic liquids or mixtures thereof containing biologi- -~` , cally decomposable contaminants and containing the equiva- ;
. :-lent of at least about 10 milligrams per liter of nitrogen , in a reduced form; particularly the ammonia form. Most municipal waste waters and industrial waste waters of equivalent strength fall within the above definition of waste water.
It is another object of the invention to ' reduce the ammonia nitrogen content of waste water -~
'~ employing a fluidized bed of biological organisms and ~ simultaneously controlling the tendency of the bed i ~ i particles to become excessively enlarged by excess biological growth.
It is an additional object to treat waste . ' ' ' : : ' ':
-7~
,.~.,., ., . .. , : , ~0574~30 , water containing significant amounts of suspended solids without effectively reducing the efficiency of the process.
A further object of the invention is to provide an efficient waste treatment process adapted to operate at lower detention times compared to traditional , ~ processes.
The aforementioned and other objects are met in a process for removing ammonia nitrogen from ~ ' waste water by generating a fluidized bed from waste ; ; water and biota,adapted to oxidize ammonia nitrogen by ~' ` use of aerobic biota attached to a solid particulate ~, carrier adapted to be fluidized; then metering sufficient .. . . .
~ ~ amounts of oxygen into the bed to allow the biota to ','~, oxidize the ammonia nitrogen content of the waste water ', ~ passing therethrough and thereafter removing excess bacterial growth formed on said carrier during the pro~
, cess.
~ The term "fluidized bed" as employed herein ~ -`i refers to the flow of a suitable liquid upwardly through ~' 1. ' , .
a bed of suitable sized particles at a velocity sufficiently ~, ' ' high to buoy the particles, to OvercQme the influence ' ,~
,~ of gravity, and to impart to ~hem an appearance of ' , movement within the bed; said bed being expanded to a '", greater depth than when no flow is passing therethrough. '~' The particles travel to different parts of the bed and are imparted with movement within the bed. On the con- ;
l , trary, in an expanded bed as employed in the prior art ,~ systems such as the systems mentioned hereinbefore in '~' .,~
~', connection with the two Weber et al publications and the ', Huether Patent No. 3,658,697, the particles are primarily `'1 substantiallY suspended in a ~iven volume by the water passing therethrough.
~f~ As waste water containing nitrogen in the :, , ~ 8 form of ammonia is passed through the fluidized bed, bacterial growth on the particle~s is accelerated and the bed particle size increases. If unchecked, the bed particles become enlarged and may agglomerate, thus reducing the biological surface area per unit folume of the reactor and the efficiency of the column. Further, the particles tend to be reduced in specific gravity as they enlarge and/or agglomerate and tend to be carried away from the bed. It is a feature of the present process that the excess cellular material or bacterial growth formed on the particles during the process is mechanically removed thereby overcoming the tendency of the particles I ~ ¦
to be carried away in the process effluent. Accordingly, ¦
the term "excess cellular material" as employed herein refers to the excess of such material attached to the particulate carrier beyond that needed for the normal operation of the system.
Employing a fluidized bed for biological treat-ment al~o p~rmits waste water containing substantial amounts of suspended matter to be treated. Such suspended matter readily passes through the fluidized bed. Other types of beds, such as packed beds, are subject to plug-ging and excess pressure losses caused by excess growth and by retention of suspended particulate matter contained i ;
in waste water.
Another substantial advantage of the present fluidized bed process is the unexpected high flow rates and removal efficiencies achieved by the fluidized system.
The process is readily adapted to meet the water and waste water purification needs of municipalities and industry.
~'', , I ' l -9 ll ~L05~30 1 ~
In view of the foregoing r this invention contem-I , plates a new and improved biological process for removing `
; 1 amm,onia nitrogen from waste water which includes i the steps of forming a fluidized bed of microorganisms - 1l attached to a solid particulate carrier, continuously passing waste water to be treated through the fluidized , I bed, adding oxygen to the fluidized bed, and retaining ! the waste water in ~he fluidized bed for a sufficient . j . .. . ............................... .
period of time, while maintaining the fluidized bed at a sufficient temperature, and while maintaining the fluidized bed under aerobic conditions to biologically .. ~ ~, I .
convert substantially all of the ammonia nitrogen to be `I removed from the waste water to oxidized forms of nitrogen, `~including nitrite and/or nitrate nitrogen, water, and j1 cellular material. The process further comprises the ~,steps of continuously withdrawing the oxidized forms of nitrogen and water from the fluidized bed, and removing excess cellular material from the particulate carrier. In ;
il another form of the inVentiQn, apparatus is provided to ; ~ effect the foregoing process.
... ,1 1 . :.
j BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a flow sheet illustrative of the process of the invention with the various processing :.
components shown more or less diagrammatically, and Fig. 2 is a flow sheet illustrative of the process of 1 a second embodiment of the invention.
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. ~ , ., , : . , ~057430 I D~SCRIPTION OF Tll~ PREFERR~D EMBODIMENTS
,j _ I
While applicable to the treatment of any fluid containing ammonia-nitrogen to which bacteria can become acclimated, the present process is most readily adapted for nitrification at secondary waste water treatment faci-1 lities. Designed for complete nitrification of wastewater, the process may also be installed at overloaded conventional trickling filtration plants or activated sludge processing facilities where BOD is being removed ; but where nitrification becomes necessary particularly ; where land availability is limited. It has far-reaching . !
capabilities to augment overloaded treatment systems.
~ Ij For most practical applications, the waste water ¦ I to be treated will contain at least the equivalent of about ;
~' ' 10 milligrams per liter of ammonia nitrogen. Of course, j , the process is able to treat waste water containing less than this amount. I
There must be sufficient oxygen in the feed waste water in order to provide the stoichiometric amount for oxidation of the ammonia to be removed. Pure oxygen or ani , oxygen cor.taining gas, such as air, may be injected into . ~j . . .
the feed preferably prior to entry of the feed into the fluidized bed. If desired, the oxygen may be injected into ~ ;~
-~ the fluidized bed or both into the feed and bed To ~ ~ ~
increase the efficiency of the oxygen transfer, the ; ~ ~1 effluent gases from the fluidized bed can be recycled into the waste water, or the waste water may be recycled to enhance greater oxygen adsorption.
By way of an example of the process, waste ~, water is passed through the up-flow fluidized bed accor-~ .
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!l , 0574;~ZO
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; ding to the invention in the presence of appropriate ;:, li ; .
microorganisms which convert am~Zonia nitrogen to oxidized forms of nitrogen, including nitrite and/or nitrate nitro-gen and cellular material. A general equation for the biological phenomenon may be expressed as follows:
C2 + NH3 ~ 2 + Microorganisms-~ N02 and/or NO
H20 ~ Microorganisms Sufficient oxygen must be present to satisfy this stoichiometric minimum in light of the amounts of ammonia `
present in the waste water. Generally, from about 3.0 to about 5.0 milligrams of dissolved oxygen are needed for each milligram of ammonia oxidized. Lesser amounts can be ~ 1 employed; however, the process generally becomes less efficient. If greater amounts are employed, then an excess of oxygen is provided which is unnecessary to the ~;
implementation of the process. In certain instances it will not be possible to accurately determine the ammonia nitrogen in the waste water. Therefore, as a practical measure it is preferable to saturate the waste water as far as practicable with dissolved oxygen. The solubility of pure oxygen is about 40 milligrams per liter at room temperature at atmospheric conditions. I -In order to provide dissolved oxygen in amounts approaching the solubility of pure oxygen it has been found that a fermentor turbine can be efficiently employed. The fermentor turbine has a hollow annular shaft with blades or turbines at the base of the shaft.
Waste wateris passed through a tank into which the fermentor turbine is disposed. Oxygen is passed through the central orifice of the turbine and is broken up into a plurality : ~... . ., ~ .
. :: , .
, ' ' ::
5~436) of tiny bubblcs by ~he spinning blades at the base of the turbine shaft. Other gas transfer devices known in the -art may also be used.
A fluidized bed system is preferably generated by passing ~aste water through an upright column containing microorganisms attached to a particulate carrier or sub-¦ strate. In general, the carriers will be seeded withbacteria from aerobic processes adapted to feed on waste water. Nitrosomonas and nitrobacter, which are naturally found in municipal waste water are particularly I preferred for this purpose.
¦ Suitable carrier material~ for the biota or microorganisms include natural or artificial materials such as coal, volcanic cinders, glass or plastic beads, ~1 sand, alumina, garnet and activated carbon particles. The ~
:!
¦ size of the particles chosen is a function of both specific 1I gravity and surface area. For the most part, the carrier particles are between about 0.2 and about 3 millimeters 1 in diameter. Employing the preferred flow rates of the l ~
¦~ present invention, enhanced results are obtained by bed ,3 :
¦! particles having a diameter of from about 0.4 to about 1.5 millimeters. The above discussion assumes the presence !
of spherical particles, but the particles in most cases would not be spherical. Most preferably, the particles are of a uniform size. While the aforesaid bed carriar materials are illustrative of the preferred substrates, nonetheless other materials, nontoxic to the bacteria, whether natural or synthetic, can be employed.
It has keen found that substantial amounts of ammonia ~3 can be aerobically nitrified in a fraction of bed, sometimes -: in the first few feet adjacent the influent feed. Accordingly, it may be sufficient to provide aerobic conditions for only a fraction of the bed height. 5imilar results are obtained for aerobic removal of B~D. Further, it is within the scope of the invention to carry out the process in this manner.
' :~
. . ,, , .", .,.:
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; For enhanced ammonia removal, the bed particles preferably have a thin layer of bacteria seeded thereon.
Preferably, the bed particles are first cultured with seed bacteria such as those present in sewage. Seeding is ' provided externally, or yreferably, internally within the ; " .
fluidized bed column. For this purpose the carrier parti-cles are introduced into the column and thereafter waste water which is to be trea~ed is fed through the column. It has been found that seeding is enhanced by recycling all - .
;
or a portion of the flow, controlling the pN and con-< I centrations of NH3 and alkalinity. Seed bacteria or bacteria naturally present in the sewage rapidly grow around the bed particles and become acclimated to the system~ The specific gravity of the seeded particles s I is preferably no less than 1.1 and preferably at least about 1.2 in order to insure that such particles are not carried out of the system during operation of the fluidized , ;I bed. I ;
-` " By way of an example of the operation, waste water, appropriately oxygenated if necessary, enters a l vertical cylindrical column through a distribution manifold , in the column base. A suitable distribution manifold i has a series of spaced apart inlet ports which regulate the flow of waste water through the column. Obviously, a wide assortment of conventional distribution manifold 'I , :
systems could be utilized also.
The pressure of the waste water influent at the point of fluidization varies depending on many factors, including the quantity of bed particles, their specific gravity and the degree of pressurization set in the column~
.i, , ; .
' i , , . I
~05743(~ 1 For the vertical column fluidized bed systems, the oxygen-ated feed is pumped into the column at a rate sufficient 'I
to support the seeded particles in the state of fluidiza-tion as hereinbefore described.
Where waste water contains highly concentrated wastes, microorganisms or occluded solids, it may be desirable to inject the oxygen at greater than atmospheric pressure. At increased pressures larger amounts of oxy-, gen are dissolved in the waste water to satisfy the increasedstoichiometric requirements. For example, amounts as great , ,l as about 150 milligrams of oxygen per liter of waste water , and more can be supplied to the feed at super atmospheric pressure. ~ ;~
In general the flow rate into the col~mn is ~J ¦~ sufficient to provide a fluidized bed according to the invention. Depending upon the size and specific gravity of ~-the bed particles, among other factors, the flow rate ,' is usually at least about 6 gallons per minute per square foot of bed. By adjusting the specific gravity of the ,' bed particles, by employing denser bed particles and !
ii~ the like, the process can be carried out at very high .1 ' ,1 flow rates, possibly even the order of hundreds of gallons per minute per square foot of bed. Commercially, it is desirable to operate at flow rates approaching 100 gallons per minute per square foot of bed. Fluidized beds operating according to the fundamental principles of the present invention have been successfully operated at flow rates of about 25 gallons per minuke per square foot of bed and operations at higher rates are well within present technology as set ~orth herein.
: . .
It has been found that enhanced results are .~ :
;
.. , , ~ .
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~L0579L3~ ;
obtained, and accordingly, it is preferred to provide a flow rate into the column from about 6 to about 40 gallons per minute per square foot of natural or artificial bed.
Further enhanced results are obtained when the flow rate is from about 8 to about 25 gallons per minute per square foot of bed. Depending upon the specific flow rate selected, the actual dwell time within the column for a volume of waste water can be as little as from about 2 to about 5 minutes. In general, the dwell time within the column is usually under about 30 minutes and most fre-quently less than about 15 minutes per up to about 12 feet of bed height, but the actual dwell time is a function of the size of the reactor. The flow rate iæ preferably adjusted to compensate for the size and specific gravity of the seed particles.
For a given bed, as the flow rate is incre~sed ;~ in order to increase the volume of waste water being `~3 ; treated, the specific bed of microorganism attached ~ particles will increase in height. In order to compensate .
for the tendency of the bed to increase in height at higher : . ~
flow rates, it is desirable to employ additional bed particles or to employ bed particles of higher specific ` gravity.
As the waste water is pumped into the column an area immediately above the distribution manifold may be ;l free of seeded particles although bed particles with sufficient growth may remain. This phenomenon has also been observed during initial seeding periods of the bed but disappeared as seeding of the carrier particles progressed.
' This interface height, then ~the height from the distri-bution manifold to the bottom of the seeded fluidized bed in a vertical column) is a function of the flow rate of the column, the temperature, the specific gravity of the bed particles and the length of time of the seeding ` ' ' - /~' :
......
period as ~ell as the nature of the distribution manifold. I
Practically, this phenomenon has a minimal effect, if any, on the column's efficiency. Generally as flow rate increases interface height increases and conversely as flow rate decreases interface height decreases.
In general~ the pH of the fluidized system will not require external manipulation. If need be, it may be adjusted to fall within the range of from about 5.5 to 9.5. Best results are obtained at a pH from about 6.0 to 9Ø The internal temperature of the fluidized column should be sufficient to permit bacterial activity. For this purpose the bed temperature is from about 5 to about 45 C. The bed temperature will vary with that of the influent waste water and, accordingly, ambient operating temperatures on the order of from about 8 to about 30 C. will be the nominal bed temperatures and are entirely satisfactory.
As the ammonia oxidation reaction proceeds in the fluidized bed, bacteria tend to grow on the surface !
;~ oE the carrier particles. After a time, if unchec~ed, bed particles tend to form thick layers and expand to the extent that they form agglomerates, and/or gelatinous masses. I 1 Should this be permitted to occur, then the surface area -' `~ per unit reactor volume available for biological reaction is great . ~ .
ly reduced and the efficiency of the process is correspondingly reduced. Further, particles tend to be carried out of the fluidized bed as their specific gravity decreases. They aldo tend to entrap or become attached to gas bubbles, such as ,: . . .... . .~:, , ~ , 1057~3(~
oxygen bubble~ from the injected source. The gas bubbles reduce the specific gravity of the particles and tend to carry them away from the bed toward the top of the column where they can collect as an undesirable floc and/or leave the system.
In order to overcome these problems excess bacterial growth is preferably mechanically removed from the particles although chemical and biological means or combinations thereof may be employed to supplement mechani-cal removal. Sufficient growth in the form of a ~hin layer of bacteria must remain on the particles in order to .i , .
` preserve the efficiency of the process. Removing all growth ~, which has been suggested in the prior art for up-flow ` expanded bed process used for treating waste water to re-move carbon by adsorption, des~roys the efficiency of the . ,, present process. In one embodiment, growth is regulated by removing predetermined quantities of bed particles from the column by a valve-controlled outlet port and mechani-cally ~gitating and abrading the particles. Thls operation may be performed in a separate abrasion vessel employing a mixer which resemh-les the rotating knife in a Waring Blender.
The abraded particles are ~hen returned to the bottom of the fluidized bed. Alternately, the particles in ~he abrasion vessel are subjected to the action of compressed air or water sprays to remove excess microorganisms. Other suitable agitation mechanisms and apparatus wiil be apparent to those skilled in the art. After treatment, the abraded particles are metered into the fluidized bed at its base by a suitable inlet port. The withdrawal of measured amounts of bed particles, their cleaning and recyling into :
. ' ' ' .- .- . , . .,.- .
. .
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Il ~057gL30 . . .
the process can be accomplished without a significant ,1 interference with the continuity of the process.
., , By way of example, in a second embodiment, bed particles are allowed to be carried out in the effluent i from the column into a set-tling tank ~rom which they are pumped into the bottom of the column. Separation of the ~j excess cellular material growth fr,om ~h,_ par~ti,_ulate~carrier ;¦ is effected by the pump. Fig. 1 illustrates this process.
Waste water and air or oxygen is introduced into a flui~
dized bsd column 10 through an inlet port 11 for treatment therein. The treated waste water containing bed particles is ~ :~
¦ exhaus~ed as at 12 from the fluidized bed column 10 into a settling tank 14. Separation of the treated waste water or .!' ,¦ effluent 16 and bed particles 18 occurs in the settling tank.
The separated bed particles are-then pumped back into the j fluidized bed column as indicated at 20. Separation of the growth from the carrier particles occurs by abrasion in a pump 22. When the mixture of the abraded carrier and the ~` !
growth or excess cellular material is pumped back into the column 10, the carrier particles will remain in the column while the excess cellular material will be carrii~d on through the system to the effluent 16.
By way of example, in a third and more preferred ~-emkodiment, the particles are treated in situ in order to remove excess bacterial growth from their outer sur-faces. It has been found that excess bacterial growth is readily removed from floc, agglomerates ard/or bed particles at the top (or downstream side) of the bed, by a sharp rotating blade or flexible agitator. These mechanisms j l ' , ' ' 'j , j . :
- 19 ~
',' ~ :' ' 79~30 .
shear the bacteria from the carrier particle and thereby remove excess growth. The stirrer provides continuous control of the height of the fluidized bed. Other mechanical mixers, ultrasonic devices, bafle plates and other abrasion-type surfaces, or even water or compressed air jets directed upwardly and sidewardly against the column walls to create agitation vortices and the like, as well as other suitable conventional agitating means, can be employed within the column.
Where the bacteria are abraded batchwise to control growth, it has been found that sufficient growth is removed, when the height of the fluidized bed after treatment is reduced on the order of from about 10 to 25 percent of its original expanded length at the same flow rate. At highly elevated or substantially reduced flow rates, the height may be somewhat above or below the afore-said range. For removal of excess growth in situ using the .. .
i' air cleaning method, for example, the flow rate to the . ~ , .
column may be reduced to about 1/3 normal flow (reduction , is dependent on operating flow rate). The bed will settle to a new lower height. Air is injected into the bed to cause abrasion. During and immediately after this abrasion, the removed growth is carried out of the reactor and exhaus-ted from the system. Thereafter, the flow rate may be increased to its normal velocity.
Depending upon the nature of the waste water and the concentration of contaminants, it may prove useful to employ more than one column connectedin series. It has been found practical in many cases to employ the effluent from '' ' .
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105743~
:` :
th~ first column as the influent feed for a second column.
Accordingly, a plural column system may provide enhanced results for treatment of industrial, municipal and other waste waters. In a two col~mn system, ammonia nitrogen is further oxidized by directing ~he effluent from the first co-lumn into the second column as the sole influent, or in combination with fresh sewage. During start-up of the column it has, in certain cases, been found useful to recycle at least a portion of the effluent treated to the column .; , .
in order to promote initial growth of bacteria on the bed carrier particles in situ.
. ! .
By way of example, Fig. 2 shows a somewhat preferred embodiment of the process according to the invention. Waste water is introduced through an inlet pipe 23, valve 24 and inlet port 25 into the Iower portion of cylindrical column 26 through a manifold 28 in the base of the column. Microorganism or biota-seeded bed particles are fluidized by the passage of waste watar thrsugh the column and form a fluidized bed 30. The interface height sf the fluidized bed is indicated at 32j forming a chamber 33 7 ' thereabsve in the column. Treated waste water or effluent is exhausted from the column after passage through the fluidized bed and chamber 33, as at 34. Then the effluent may be passed thrsugh an effluent purifier 35 such as a settling tank or for treatment with flocculants or the like, ~;;
if necessary. Selected portions of the effluent,as xequired, ;~
are recycled through pipe line 36, containing a pump 37, to the influent waste water inlet port 25. This serves the i~
following purposes: (13 to promote growth of the biota or ~
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~057~3~
' ; ~ .
microorganisms on the particles during seeding operations;
(2) to maintain uniform flow where input flow decreases;
(3) to dilute the concentration of ammonia into the bed, if necessary to provide uniform concentration of waste water; (4) to provide more oxygen to the waste water; (5) to permit additional removal of ammonia remaining in the efflu-ent. Oxygen is metered through an inlet pipe 38 and valve 40 into a mixing chamber 41 and then into the waste water inlet port 25 in sufficient amounts to satisfy the biological reaction for the oxidation of the ammonia. The metering of sufficient amounts of oxvgen may be conducted automatically by providing a conventional oxygenating system, such as the UNOX process of Union Carbide, Inc. In some installations, in addition to the oxygen supplied through inlet pipe 3B, or as an alternative thereto, oxygen ls metered through . .~ ;
inlet pipe 42, valve 44 and inlet port 46, direc~ly into the `~ fluidized bed 30. In order-to faoilitate the dissolution ~ of relatively large quantities of oxygen into the waste ; water, the system may be pressurized to several atmospheres of pressure or more. Additionally, effluent gas, if any, may be recycled. Provision can be made for metering in - oxygen in response to the output o~ an oxygen ana yzer (not shown) placed within the bed, in the effluent line or adjacent the feed, if desired.
~uring treatment, bacterial growth on the ~ ;
particles is monitored as a function of bed expansion by a conventional optical device or other type of solids sensor 480 ~hen bed expansion reaches a predetermined height ~whereby the sensor device is activated, the bed particles are regenerated by abrasion or the like to remove excess ~' . , .
.
! ~ ' . , ~ ', ,. .. .
: ~057~i30 growth. A mechanical stirrer assembly 5n is preferably provided at the top of the column to remove excess growth of the cellular material. The stirrer is in the form of sharp rotating blades or is formed from a flexible length of synthetic polymeric material, polyethylene tubing, as desired.
In some installations it is desirable to employ an upwardly-outwardly directed conical portion at the upper end of the Fluidized bed column to reduce the upward flow velocity to prevent the bed particles from being carried off in the eFfluent, among other desirable features. Further, . this feature serves at least as an assisting means for , controlling the growth on the bed particles.
In some installations, the present process can be employed to provide the nitrified feed, or otherwise uti-lized in cooperation with a carbon-denitrif1cation process. ~;
Further, the present process can be utilized to provide ~5 feed for the denitrification process set forth in Canadian patent No. 986,239, issued March 23, 1976.
Further, in some installations, it is possible to employ a plurality of stages in a single fluidized bed column. The first or lowermost stage of the column is ~ maintained in such condition as to remove BOD aerobically, :~ the second stage in the column is maintained in such ' ' '~.:
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~ 23 ~
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~574~ ~
condition as to remove BOD aerobically; the third stage i5 maintained in such condition as to effect nitrification of the waste products; and the fourth stage is maintained in ~uch condition as to effect denitrification of the waste products. Further, various recycle means may be employed to recycle at least a portion of the products through one or more of the stages. All or some of the forgoing stages may be employed in a single fluidized bed column. It should be recognized that it may be possible to carry out more than one of the above processes simultan-eously in a single stage of a multiple system. It will ;`:. !
also be appreciated that the foregoing sequence of stages may be varied, if desired.
; EXAMPLE OF INVENTION
To demonstrate the process a number of tests were made as indicated hereinafter using a 12 foot high, ; by 3 inch diameter Plexiglas~ olumn. Sand of a silica ~ ~
composition of about 0.4 to 0.8 mm size was used upon which ~ - "
to grow the nitrifving organisms. The synthetic waste ``
water was fed into the bottom of the column and taken out at the top. The synthetic waste consis~ed of tap water , to which ammonia and bicarbonate were added as major ingredients, and phosphorus to a lesser degree. During the , test period the height of the fluidized bed was about 5O5 feet, the influent flow was 1800 milliliters/min. and the temperature averaged 21C.
'- ' '. ' ~':
':: ' ' ~ ' . . : : ::
~ 105743~
NITRIFIC~TION TE5T DATA
DISSOLVED 2 pH NITRATE-N NITRITE-N
TEST INF. EEE'. INF. EFF. _NF. EFF. INF. EFF
1 8.4 0.3 7.1 6.6 1.6 4.2 1.7 4.4 2 ~.1 0.4 7.6 6.3 1.6 4.1 0.~ 4.3 ; 3 8.2 0.6 8.0 7.0 0.7 3.3 0.8 3.9
inlet pipe 42, valve 44 and inlet port 46, direc~ly into the `~ fluidized bed 30. In order-to faoilitate the dissolution ~ of relatively large quantities of oxygen into the waste ; water, the system may be pressurized to several atmospheres of pressure or more. Additionally, effluent gas, if any, may be recycled. Provision can be made for metering in - oxygen in response to the output o~ an oxygen ana yzer (not shown) placed within the bed, in the effluent line or adjacent the feed, if desired.
~uring treatment, bacterial growth on the ~ ;
particles is monitored as a function of bed expansion by a conventional optical device or other type of solids sensor 480 ~hen bed expansion reaches a predetermined height ~whereby the sensor device is activated, the bed particles are regenerated by abrasion or the like to remove excess ~' . , .
.
! ~ ' . , ~ ', ,. .. .
: ~057~i30 growth. A mechanical stirrer assembly 5n is preferably provided at the top of the column to remove excess growth of the cellular material. The stirrer is in the form of sharp rotating blades or is formed from a flexible length of synthetic polymeric material, polyethylene tubing, as desired.
In some installations it is desirable to employ an upwardly-outwardly directed conical portion at the upper end of the Fluidized bed column to reduce the upward flow velocity to prevent the bed particles from being carried off in the eFfluent, among other desirable features. Further, . this feature serves at least as an assisting means for , controlling the growth on the bed particles.
In some installations, the present process can be employed to provide the nitrified feed, or otherwise uti-lized in cooperation with a carbon-denitrif1cation process. ~;
Further, the present process can be utilized to provide ~5 feed for the denitrification process set forth in Canadian patent No. 986,239, issued March 23, 1976.
Further, in some installations, it is possible to employ a plurality of stages in a single fluidized bed column. The first or lowermost stage of the column is ~ maintained in such condition as to remove BOD aerobically, :~ the second stage in the column is maintained in such ' ' '~.:
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~ 23 ~
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~574~ ~
condition as to remove BOD aerobically; the third stage i5 maintained in such condition as to effect nitrification of the waste products; and the fourth stage is maintained in ~uch condition as to effect denitrification of the waste products. Further, various recycle means may be employed to recycle at least a portion of the products through one or more of the stages. All or some of the forgoing stages may be employed in a single fluidized bed column. It should be recognized that it may be possible to carry out more than one of the above processes simultan-eously in a single stage of a multiple system. It will ;`:. !
also be appreciated that the foregoing sequence of stages may be varied, if desired.
; EXAMPLE OF INVENTION
To demonstrate the process a number of tests were made as indicated hereinafter using a 12 foot high, ; by 3 inch diameter Plexiglas~ olumn. Sand of a silica ~ ~
composition of about 0.4 to 0.8 mm size was used upon which ~ - "
to grow the nitrifving organisms. The synthetic waste ``
water was fed into the bottom of the column and taken out at the top. The synthetic waste consis~ed of tap water , to which ammonia and bicarbonate were added as major ingredients, and phosphorus to a lesser degree. During the , test period the height of the fluidized bed was about 5O5 feet, the influent flow was 1800 milliliters/min. and the temperature averaged 21C.
'- ' '. ' ~':
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~ 105743~
NITRIFIC~TION TE5T DATA
DISSOLVED 2 pH NITRATE-N NITRITE-N
TEST INF. EEE'. INF. EFF. _NF. EFF. INF. EFF
1 8.4 0.3 7.1 6.6 1.6 4.2 1.7 4.4 2 ~.1 0.4 7.6 6.3 1.6 4.1 0.~ 4.3 ; 3 8.2 0.6 8.0 7.0 0.7 3.3 0.8 3.9
4 8.6 0.7 7.6 7.0 0.7 2.6 0.8 3.2 8.6 0.5 7.4 6.6 1.8 3.6 0.7 4.3 6 9.8 0.8 8.1 7.1 1.8 5.8 0.6 ~.4 7 8.5 0.5 7.6 6 9 0.6 5.5 0.1 0.1 AVERAGE ~.7 0.5 7.6 6.8 1.3 4.2 0.7 3.8 , ~:
l At the flow rate of 9.7 gallons per minute per square '! ~ foot, the detention time in the 5.5 foot fluidized bed was less than 5 minutes. It can readily be seen that oxygen was limiting the process as only 0.5 mg/l was left ~-, in the effluent and if pure 2 had been used re ammonia ' .~.~ . . . ..
'`J~ could have been nitrified. Also, only half or less of ~ the column was seeded during this test period and much . ~ ~ , . .
. ' greater nitrification would be expected for a fully seeded --`~ column. In effect, 6 mg/l of NO2-N ~ NO3-N were pro- ~ `
~` duced in this short time period which is truly signi- ~
-' ficant in light of the long detention periods normally ~ ;
required with prior art processes.
The presently preferred embodiments of the inven~
tion have been described for purposes of explanation. It ; should be understood that modifications ma~ be made therein as will appear evident to those skilled in the art to which ~t ~ ' ' '' ' ' :i , . : ' ,; ' ~:
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~ ~57430 the invention pertains. It is therefore, intended to : , encompass all such changes as fall within the true spirit of the invention.
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l At the flow rate of 9.7 gallons per minute per square '! ~ foot, the detention time in the 5.5 foot fluidized bed was less than 5 minutes. It can readily be seen that oxygen was limiting the process as only 0.5 mg/l was left ~-, in the effluent and if pure 2 had been used re ammonia ' .~.~ . . . ..
'`J~ could have been nitrified. Also, only half or less of ~ the column was seeded during this test period and much . ~ ~ , . .
. ' greater nitrification would be expected for a fully seeded --`~ column. In effect, 6 mg/l of NO2-N ~ NO3-N were pro- ~ `
~` duced in this short time period which is truly signi- ~
-' ficant in light of the long detention periods normally ~ ;
required with prior art processes.
The presently preferred embodiments of the inven~
tion have been described for purposes of explanation. It ; should be understood that modifications ma~ be made therein as will appear evident to those skilled in the art to which ~t ~ ' ' '' ' ' :i , . : ' ,; ' ~:
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~ ~57430 the invention pertains. It is therefore, intended to : , encompass all such changes as fall within the true spirit of the invention.
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Claims (22)
1. A biological process for removing ammonia nitrogen from waste water, which comprises forming a fluidized bed of microorganisms attached to a solid particulate carrier, continuously passing waste water to be treated through said fluidized bed, adding oxygen to said fluidized bed, retaining said waste water in said fluidized bed for a sufficient period of time while maintaining said fluidized bed at a sufficient temperature and while maintaining said fluidized bed under aerobic conditions to biologically convert substantially all of the ammonia nitrogen to be removed from the waste water to oxidized forms of nitrogen, water and cellular material, and continuously withdrawing said oxidized forms of nitrogen and water from said fluidized bed, and removing excess of said cellular material from said particulate carrier.
2. A biological process for removing ammonia nitrogen from waste water, according to claim 1, where-in said step of removing excess of said cellular material from said particulate carrier is effected at the downstream portion of said fluidized bed by rotating a sharp blade or flexible stirrer.
3. A biological process for removing ammonia nitrogen from waste water according to claim 1, wherein said particulate carrier is first cultured with seed bacteria externally of said fluidized bed to form said microorganisms.
-claim page 1-
-claim page 1-
4. A biological process for removing ammonia nitrogen from waste water according to claim 1, wherein said particulate carrier is first cultured with seed bacteria internally of said fluidized bed to form said microorganisms.
5. A biological process for removing ammonia nitrogen from waste water according to claim 1, further comprising the step of continuously recycling at least a portion of said waste water through said fluidized bed.
6. A biological process for removing ammonia nitrogen from waste water according to claim 5 further comprising the step of adding oxygen to said portion being recycled.
7. A biological process for removing ammonia nitrogen from waste water according to claim 1, further comprising passing said waste water to be treated sequen-tially through a series of fluidized beds and biologically processing said waste water in each of the beds accor-ding to the steps of claim 1.
8. A biological process for removing ammonia nitrogen from waste water according to claim 1, wherein said waste water to be processed contains at least about 10 milligrams of ammonia nitrogen per liter and wherein the flow rate of said waste water through said fluidized bed -claim page 2-is upwardly at least about 6 gallons per minute per square foot of fluidized bed, and wherein the dwell time of said waste water in said fluidized bed is less than about 15 minutes per up to 12 feet of bed height, and wherein said carrier has a particle diameter of from about 0.2 to about 3 millimeters and a specific gravity of at least about 1.1.
9. A biological process for removing ammonia nitrogen from waste water according to claim 1, wherein said waste water contains at least up to about 10 milligrams of ammonia nitrogen per liter and the flow rate of said waste water through said fluidized bed is upwardly between about 6 and about 40 gallons per minute per square foot of fluidized bed, and wherein the dwell time of said waste water in said fluidized bed is less than about 15 minutes per up to about 12 feet of bed height, and wherein said carrier has a particulate diameter of from about 0.4 to about 1.5 millimeters and a specific gravity of at least about 1.4 and wherein the pH value of the fluidized bed is between about 505 and about 9.5 and wherein the temperature of the fluidized bed is between about 5° and about 45°C.
10. A biological process for removing ammonia nitrogen from waste water according to claim 1 wherein said particulate carrier is one of a group consisting of coal, volcanic cinders, glass t plastic beads, sand, garnet, activated carbon and alumina.
-claim page 3-
-claim page 3-
11. A biological process for removing ammonia nitrogen from waste water according to claim 1 wherein said oxygen is added to the influent waste water prior to entering the fluidized bed.
12. A biological process for removing ammonia nitrogen from waste water according to claim 1 wherein said oxygen is added directly to the fluidized bed.
13. A biological process for removing ammonia nitrogen from waste water according to claim 1 wherein said oxygen is simultaneously added to the influent waste water prior to entering the fluidized bed and directly to the fluidized bed.
14. A biological process for removing ammonia nitrogen from waste water according to claim 1, wherein from about 3.0 to about 5.0 milligrams of dissolved oxygen are added for each milligram of ammonia to be removed from the waste water.
15. A biological process for removing ammonia nitrogen from waste water, which comprises forming a fluidized bed of microorganisms attached to a solid particulate carrier, continuously passing waste water to be treated through said fluidized bed, adding oxygen to said fluidized bed, retaining said waste water in said fluidized bed for a sufficient period of time while maintaining said fluidized bed at a sufficient temperature and while maintaining said fluidized bed under aerobic conditions to biologically convert substantially all of the ammo-nia nitrogen to be removed from the waste water to oxi--claim page 4-dized forms of nitrogen, water and cellular material, continuously withdrawing said oxidized forms of nitrogen and water from said fluidized bed, and withdrawing from said fluidized bed so said processed waste water together with at least some parti-culate carrier having excess cellular material thereon and passing same to a settling tank, retaining said so processed waste water together with said particulate carrier having excess cellular material thereon in said settling tank for a sufficient .
period of time to allow said particulate carrier having excess cellular material thereon to settle to the bottom of the tank, withdrawing said so processed waste water from the top of said settling tank, withdrawing said particulate carrier having excess cellular material thereon from the bottom of the settling tank and passing it through pumping means to effect separation of the excess cellular material from the particulate carrier, and passing the mixture of particulate carrier and excess cellular material back into the fluidized bed to mix the so separated excess cellular material with the waste water to be treated.
period of time to allow said particulate carrier having excess cellular material thereon to settle to the bottom of the tank, withdrawing said so processed waste water from the top of said settling tank, withdrawing said particulate carrier having excess cellular material thereon from the bottom of the settling tank and passing it through pumping means to effect separation of the excess cellular material from the particulate carrier, and passing the mixture of particulate carrier and excess cellular material back into the fluidized bed to mix the so separated excess cellular material with the waste water to be treated.
16. Apparatus for biologically removing ammonia nitrogen from waste water, the combination comprising an elongated, substantially vertically disposed container, a manifold disposed towards the bottom of said container, -claim page 5-inlet means for said manifold for receiving waste water to be processed, a fluidized bed of microorganisms attached to a solid particulate carrier disposed in said container above said manifold, means for adding oxygen to said flui-dized bed, said fluidized bed being arranged to receive said waste water from said manifold and biologically con-vert substantially all of the ammonia nitrogen to be removed from the waste water to oxidized forms of nitrogen, water and cellular material, outlet means for said con-tainer for continuously withdrawing the so processed waste water, oxidized forms of nitrogen, and means for removing excess cellular material from said particulate carrier.
17. Apparatus for biologically removing ammonia nitrogen from waste water according to claim 16 wherein said means for removing excess cellular material from said particulate carrier is a mechanical stirrer mounted on said container to extend into the upper portion of said fluidized bed.
18. Apparatus for biologically removing ammonia nitrogen from waste water according to claim 16 further comprising a solids sensor means for actuating said means for removing excess cellular material from said particulate carrier when said fluidized bed exceeds a predetermined height.
-claim page 6-
-claim page 6-
19. Apparatus for biologically removing ammonia nitrogen from waste water according to claim 16 further comprising means for interconnecting said inlet means for said manifold with said outlet means for said container in fluid flow communication, and valve means for controlling the flow in said means for interconnecting and pump means for recycling treated waste water through said interconnecting means.
20. Apparatus for biologically removing ammonia nitrogen according to claim 16 wherein said particulate carrier is one of a group consisting of coal, volcanic cinders, glass, plastic beads, garnet, activated carbon and alumina.
21. Apparatus for biologically removing ammonia nitrogen from waste water according to claim 16 wherein said means for adding oxygen to said fluidized bed includes piping means for directly adding oxygen to said fluidized bed.
-claim page 7-
-claim page 7-
22. Apparatus for biologically removing ammonia nitrogen from waste water, the combination comprising an elongated substantially vertically disposed container, a manifold disposed towards the bottom of said container, inlet means for said manifold, a first inlet pipe interconnecting a source of waste water to said inlet means, valve means in said first inlet pipe for controlling the flow therein, a second inlet pipe interconnecting a source of oxygen to said inlet means, said inlet means including a mixing chamber, valve means in said second inlet pipe for controlling the flow therein, a fluidized bed of microorganisms attached to a solid particulate carrier disposed in said container above said manifold to receive a mixture of said waste water and oxygen from said manifold and biologically convert substantially all of the ammonia nitrogen to be removed from said mixture to oxidized forms of nitrogen, water, and cellular material, and outlet means for said container towards the upper end thereof for continuously withdrawing the so processed waste water, oxidized forms of nitrogen, and means for removing excess cellular material from said particulate carrier.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48797274A | 1974-07-12 | 1974-07-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1057430A true CA1057430A (en) | 1979-06-26 |
Family
ID=23937858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA231,116A Expired CA1057430A (en) | 1974-07-12 | 1975-07-09 | Apparatus and process for removing ammonia nitrogen from waste water |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5131063A (en) |
BE (1) | BE831247A (en) |
CA (1) | CA1057430A (en) |
CH (1) | CH616639A5 (en) |
DE (1) | DE2531110A1 (en) |
FR (1) | FR2277780A1 (en) |
GB (1) | GB1520895A (en) |
NL (1) | NL7508305A (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51122946A (en) * | 1975-04-18 | 1976-10-27 | Ebara Infilco Co Ltd | Process for treating sewages |
JPS51122942A (en) * | 1975-04-18 | 1976-10-27 | Ebara Infilco Co Ltd | Process for treating sewage water |
JPS51122941A (en) * | 1975-04-18 | 1976-10-27 | Ebara Infilco Co Ltd | Process for treating sewage water |
JPS5295870A (en) * | 1976-02-06 | 1977-08-11 | Mitsui Eng & Shipbuild Co Ltd | Biochemical nitrification reaction method |
JPS52142859A (en) * | 1976-05-21 | 1977-11-29 | Iida Kousaku | Drain treating method |
JPS53115563A (en) * | 1977-03-18 | 1978-10-09 | Meidensha Electric Mfg Co Ltd | Apparatus for treating sewage |
JPS5473461A (en) * | 1977-11-24 | 1979-06-12 | Inoue Japax Res Inc | Improved device for treating water |
JPS54107156A (en) * | 1978-02-08 | 1979-08-22 | Tokichi Tanemura | Fluidized bed type biological treatment device |
JPS55132695A (en) * | 1979-03-28 | 1980-10-15 | Toyobo Co Ltd | Fluidized bed type waste water treatment |
DE3032882A1 (en) * | 1980-09-01 | 1982-04-15 | Linde Ag, 6200 Wiesbaden | METHOD AND DEVICE FOR BIOLOGICAL WASTE WATER TREATMENT |
GB0124433D0 (en) | 2001-10-11 | 2001-12-05 | Univ Manchester Metropolitan | Improvemnts in or relating to fluid bed expansion and fluidisation |
CN114835255B (en) * | 2022-05-24 | 2023-06-13 | 湖南五方环境科技研究院有限公司 | Composite bioreactor based on iron-carbon carrier and preparation and sewage treatment method thereof |
-
1975
- 1975-07-09 GB GB2893175A patent/GB1520895A/en not_active Expired
- 1975-07-09 CA CA231,116A patent/CA1057430A/en not_active Expired
- 1975-07-10 CH CH905675A patent/CH616639A5/en not_active IP Right Cessation
- 1975-07-11 NL NL7508305A patent/NL7508305A/en not_active Application Discontinuation
- 1975-07-11 JP JP8519075A patent/JPS5131063A/ja active Pending
- 1975-07-11 DE DE19752531110 patent/DE2531110A1/en not_active Withdrawn
- 1975-07-11 BE BE2054457A patent/BE831247A/en not_active IP Right Cessation
- 1975-07-11 FR FR7521831A patent/FR2277780A1/en active Granted
Also Published As
Publication number | Publication date |
---|---|
BE831247A (en) | 1975-11-03 |
CH616639A5 (en) | 1980-04-15 |
NL7508305A (en) | 1976-01-14 |
FR2277780B1 (en) | 1979-07-20 |
JPS5131063A (en) | 1976-03-16 |
FR2277780A1 (en) | 1976-02-06 |
DE2531110A1 (en) | 1976-01-22 |
GB1520895A (en) | 1978-08-09 |
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