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Conventional wastewater treatment of nitrogen (consisting primarily of ammonium and nitrate) uses the twin processes of nitrification to transform ammonium to nitrate, and then the separate denitrification process to transform nitrate to di-nitrogen gas. These processes require two completely different sets of environmental conditions and infrastructures; can use large amounts of energy; may utilize significant quantities of chemicals such as methanol; and require skilled maintenance. The combined construction, operation, and maintenance impacts have resulted in high economic costs. In addition to economic considerations, there are significant environmental impacts associated with the current level of treatment. Nitrate pollution attributed to sewage, fertilizers, and industrial processes has caused widespread environmental damage on a global scale, including some severe societal impacts.
Ammonium removal by zeolite has been used commercially for over 30 years, and ammonium immobilization by zeolite is well documented and highly effective. The process was never popular, however, because of the need to periodically shut down the system to either remove and replace the zeolite, or to artificially regenerate the zeolite (by brine, air-stripping, etc). Traditional zeolite systems merely removed ammonium from solution, and further processes were required to convert it to nitrate or di-nitrogen gas.
The present invention is radically different because the microbial activity ensures the zeolite never becomes saturated and is therefore continually available to keep immobilizing ammonium. The system converts the ammonium to an end product of di-nitrogen gas which is released to the atmosphere. The system is a sustainable bio-zeolite reactor, running at full functionality at all times.
1. Field of the Invention
The present invention is in the field of wastewater treatment. More particularly, the present invention is in the field of nitrogen nutrient removal (ammonium, nitrite and nitrate).
2. Description of Prior Art
U.S. Pat. No. 4,098,690: Describes a process using ion exchange to reduce ammonia content of wastewaters. However the ion exchanger becomes saturated and has to be regenerated by concentrated salt solution and nitrifying bacteria. This requires the process to be shut down for regeneration, and the end-product is nitrate (a pollutant).
U.S. Pat. No. 4,522,727: Describes a process for removing ammoniacal nitrogen from aquaculture systems using zeolite. However the zeolite becomes saturated and has to be regenerated by heating to between 350° C. and 650° C. to strip ammonia. This requires the process to be shut down and the zeolite dried, heated, and re-generated, requiring significant energy.
U.S. Pat. No. 6,080,314: Describes a process using zeolite to remove nitrogen contaminants from septic systems. However the zeolite becomes exhausted and has to be regenerated by cations to displace the ammonia, or by heating, or by nitrifying bacteria. This requires the process to be shut down for regeneration, and the end-product is nitrate (a pollutant), or ammonia gas released by heating processes requiring significant energy.
U.S. Pat. No. 7,452,468: Describes a process of intermittent or continuous feeding of suspended zeolite powder to increase surface area, in conjunction with unspecified biological material. Zeolite volume is fed at ratio of 20 parts per million compared to system volume, and can increase bacterial residence time, nitrification, denitrification and carbonaceous processes. However this process is a performance enhancer for malfunctioning existing systems, not a stand-alone treatment system, not a fixed film zeolite reactor, and does not contain anammox.
Van de Graaf A. A., A. Mulder, P. de Bruijn, M. S. M. Jetten, L. A. Robertson, J. G. Kuenen. 1995. Anaerobic oxidation of ammonium is a biologically mediated process. Applied and Environmental Microbiology, April 1995, 1246-1251.
Van Dongen U., M. S. M. Jetten, M. C. M. van Loosdrecht. 2001. The Sharon-Anammox process for treatment of ammonium rich wastewater. Water Science and Technology, Vol 44 No 1, 153-160.
Van der Star W. R. L., W. R. Abma, D. Blommers, J. Mulder, T. Tokutomi, M. Strous, C. Picioreanu, M. C. M. van Loosdrecht. 2007. Startup of reactors for anoxic ammonium oxidation: Experiences from the first full-scale anammox reactor in Rotterdam. Water Research, 41 (2007), 4149-4163.
The present invention uses zeolite media (or similar alternatives with high cation exchange capacity such as ion exchange resins or synthetic zeolites) to immobilize ammonium by cation exchange. The positively charged ammonium ions (NH4) are attracted to the zeolite because it is negatively charged. The system works with many different types of zeolite, but clinoptilolite is a good choice because it is abundant and preferentially adsorbs ammonium over most other cations. However, the choice of the media will usually be determined by the transport costs—i.e. the closest source. This invention is unique because it uses microbial activity to continually regenerate the zeolite, and forms a self-regenerating system. The micro-organisms colonize the zeolite and ingest the ammonium, thereby continually freeing up the cation exchange sites to immobilize more ammonium—forming a continuous self-sustaining cycle of regeneration.
Depending on conditions the microbial population includes primarily anammox bacteria and nitrifying bacteria, but also includes denitrifying bacteria and archaea:
Anammox—There are several genera of anammox bacteria and many different anammox species—each adapted for different ecological niches. However all anammox “eat” ammonium as their food source, combining ammonium with nitrite to produce di-nitrogen gas, water, and energy per the equation:
NH4+NO2→N2+2H2O*.
Although the combination of nitrite and ammonium is the most advantageous to anammox for energy production, anammox can also combine ammonium and nitrate to form nitrogen gas per the equation:
4NH4+4NO3→4N2+8H2O+2O2*.
(*Note: these are the simplified equations—see References for detailed equations). Examples of anammox bacteria may include, but are not limited to, the following genera: Brocadia, Kuenenia, Anammoxoglobus, Jettenia.
Nitrifiers—Nitrifying bacteria oxidize ammonium to nitrate. However this is a two step process, with nitrite as the intermediate step: NH4→NO2→NO3. The conversion of nitrite to nitrate (i.e. the second step) generally happens quickly, typically within 30 minutes). Examples of nitrifying bacteria may include, but are not limited to, the following genera: Nitrosomonas, Nitrospira, Nitrosococcus, Nitrosolobus (first stage nitrification—NH4 to NO2); and Nitrobacter, Nitrospina, Nitrococcus (second stage nitrification—NO2 to NO3).
Anammox-nitrifier symbiosis—The predominant bacterial activity is the symbiosis between the nitrifiers and the anammox. One of the key features of this invention is the establishment of an extensive oxycline (i.e. boundary between aerated and anoxic zones) allowing bacteria from different zones to exist in close proximity. The first stage of nitrification converts ammonium to nitrite (NH4→NO2). The nitrite then diffuses through the oxycline where anammox combine nitrite with more ammonium to form di-nitrogen gas and water.
Denitrifiers—If BOD is present then denitrifiers can use nitrate as an oxygen source resulting in the conversion of nitrate to nitrogen gas. The importance of denitrification is generally low in this system, but the design can be modified to enhance the role of denitrification. Examples of denitrifying bacteria may include, but are not limited to, the following genera: Thiobacillus, Micrococcus, Paracoccus, Pseudomonas.
Archaea and others—there are several species of archaea that are believed to perform a similar role to anammox, but generally at low ammonium concentrations. Archaea are not well understood or documented but will undoubtedly be present in this system, albeit at low concentrations. Examples of archaea may include, but are not limited to, the following phyla: Crenarchaeota, Euryarchaeota.
Other organisms such as fungi can be present, but they do not generally have a significant role in ammonia removal.
The invention is a green, self-sustaining treatment system with low infrastructure costs and low energy usage. The design focus is to produce a robust system with minimal maintenance requirements. Nitrogen removal can be carried out at any scale, and the process encourages reduced economic, environmental, and societal impacts.
The present invention provides a natural systemic regeneration of the zeolite, and can also directly convert the ammonium to nitrogen gas—this bypasses the conversion of ammonium to nitrate and therefore prevents nitrate pollution. The system described herein optimally has one or more of the following traits:
This invention provides in one instance a system for biologically regenerating zeolite in-situ such that the process is continuous and sustainable, and may run indefinitely without the need for artificial regeneration. The zeolite has two main functions—firstly it immobilizes ammonium ions by cation exchange therefore providing a food source for ammonia-eating bacteria; secondly the ability of zeolite to “wick up” water provides sufficient aeration to oxidize the ammonia optimally, with or without additional or artificial aeration.
The system is set up to provide an environment to encourage the growth of anammox bacteria; high concentrations of nitrifiers and anammox will likely provide the most efficient treatment method. Although the system can work with just nitrifiers and denitrifiers (under high BOD loadings the denitrification process could become significant), the system would continue to function as designed. In most situations, however, the anammox will outcompete the denitrifiers in this system, but both forms of bacteria will be present regardless of which type predominates.
The “action layer” of the system is the oxycline between aerated 201 and non-aerated 202 layers.
Nitrifiers and anammox are in close proximity on their respective sides of the oxycline, enabling some of the nitrite produced by the first stage of nitrification to be used by the anammox before it is converted to nitrate. In this situation the anammox are competing with the second stage denitrifiers for the nitrite, and the more nitrite used by anammox the more efficient system. Below the action layer in the anaerobic/anoxic zone 202 is an environment containing minimal oxygen, where anammox combine ammonium with either nitrite or nitrate that diffuses or percolates down from the action layer. The lower part of the submerged layer 202 serves as an anaerobic polishing layer, as a repository of sludge & particulate matter, and as a water reservoir if the surface level varies through irregular flows etc.
This application claims the benefit of provisional patent application No. 61/738,441, filing date Dec. 18, 2012.
Number | Date | Country | |
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20150151996 A1 | Jun 2015 | US |
Number | Date | Country | |
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61738441 | Dec 2012 | US |