The primary limitations in the widespread use of methane gas to produce energy include the cost of its chemical purification and challenges of handling a gaseous phase stream. One possible mechanism to overcome these limitations is to convert methane to a more readily usable liquid-fuel such as methanol. Currently in the United States, methanol is produced through chemically catalyzed conversion of methane gas. However, the chemical technologies to convert methane to methanol are not the most economical. Additionally, sources of methane such anaerobic digester gas still need purification prior to chemical conversion to methanol.
The United States is investing significant resources to become a leader in bio-based fuels and energy. While ethanol has been of primary focus, it should be noted that other biofuels such as methanol can be also equally if not even more attractive. Methanol is widely used as an additive in gasoline blends, as an electron donor in fuel cells, as a trans-esterfication agent to convert long-chain fatty acids and lipids to biodiesel and as a precursor to synthesize dimethyl ether (DME). In addition, methanol is still one of the most widely used chemicals for enhancing denitrification in wastewater treatment. Most methanol in the United States is produced by chemical oxidation of methane. The chemical catalysis pathway is expensive, energy intensive, and redundant; involving initial oxidation of methane to carbon dioxide and hydrogen and then reduction of carbon dioxide back to methanol.
Methane is typically the primary energy substrate for methane oxidizing bacteria. However, methane oxidizing bacteria oxidize methane completely to carbon dioxide, which again is gaseous and cannot be directly used as a biofuel. On the other hand, ammonia oxidizing bacteria, which “co-metabolize” methane can only partially oxidize it to methanol (and trace amounts of formaldehyde). Based on known genomes of ammonia oxidizing bacteria, they in fact completely lack the capacity to produce carbon dioxide from methane. Additionally, carbon dioxide, which often limits direct combustion of digester gas, is used by ammonia oxidizing bacteria as a growth substrate, i.e., by fixing it to produce more cells. As shown schematically in
The drawings show embodiments of the disclosed subject matter for the purpose of illustrating the invention. However, it should be understood that the present application is not limited to the precise arrangements and instrumentalities shown in the drawings, wherein:
Referring now to
Reactor 102 contains biomass 104. A portion of biomass 104 includes ammonia oxidizing bacteria 116 in wild type and genetically modified forms, which have ammonia monooxygenase enzymes and hydroxylamine oxidoreductase enzymes. In some embodiments, bacteria 116 include at least one or several of N. europaea, N. eutropha, N. oligotropha, Nitrosospira multiformis as well as nitrite oxidizing bacteria, Nitrobacter winogradskyi and Nitrospira spp. as needed.
Referring now to
Fortuitous oxidation of organic compounds is also achieved by ammonia oxidizing bacteria: In addition to oxidizing ammonia, ammonia oxidizing bacteria can also oxidize other non-substrate-organic compounds, including methane and various other hydrocarbons. This is because of the poor substrate specificity of the enzyme ammonia monooxygenase (AMO). The ability of AMO to oxidize methane is thought to be because of its close relation to methane monooxygenase (MMO) from an evolutionary perspective. MMO is used by methane oxidizing bacteria for energy production.
In methods and systems according to the disclosed subject matter, ammonia oxidizing bacteria are preferred over methane oxidizing bacteria to oxidize methane to methanol. Since methane is the primary energy substrate for methane oxidizing bacteria, they oxidize methane completely to carbon dioxide, which cannot be used as a fuel. On the other hand, methane is not the primary energy substrate for ammonia oxidizing bacteria. Ammonia oxidizing bacteria lack the capacity to produce carbon dioxide from methane and instead only oxidize methane partially to methanol, which can be used as a fuel.
Referring again to
Sources of ammonia 106, non-substrate-organic compound 107 including methane 108, and oxygen 110 are fluidly connected to and supplied to reactor 102 via a conduit 118, e.g., pipe, etc. In some embodiments, compound 107 includes hydroxylamine 109 and carbon dioxide.
Control sub-system 112 is connected with reactor 102 and the sources of ammonia 106, compound 107, and oxygen 110. Control sub-system 112 is configured to provide/direct particular amounts of ammonia 106, compound 107, and oxygen 110 such that the ammonia is oxidized using the ammonia monooxygenase enzymes in ammonia oxidizing bacteria 116 to generate hydroxylamine. The hydroxylamine is oxidized using the hydroxylamine oxidoreductase enzymes in bacteria 116 to form nitrite. Finally, methane 108 in compound 107 is partially oxidized using the ammonia monooxygenase enzymes in ammonia oxidizing bacteria 116 to generate methanol 114.
In some embodiments, system 100 includes a methanol collection sub-system 119 having one or more filters 120 for separating methanol 114 from other constituents in reactor 102 and a compartment 122 for storing the methanol.
In some embodiments, system 100 includes a source of reductant 124 such as hydroxylamine in addition to that contained in ammonia 106. Reductant 124 is fluidly connected with reactor 102 via a conduit 126, e.g., piping, etc.
In some embodiments, system 100 includes a sparging sub-system 128 for supplying compound 107 and oxygen 110 to reactor 102 by continuously sparging the compound and the oxygen into biomass 104.
Referring now to
Methods and systems according to the disclosed subject matter enable the harnessing of digester gas into an operationally useful biofuel or external COD source in the form of methanol. Essentially by ‘integrating’ the microbial nitrogen and carbon cycles it is possible to simultaneously address nitrogen pollution (by conversion to nitrite using ammonia oxidizing bacteria) and channeling the methanol that ammonia oxidizing bacteria produce either to biofuel or using it to enhance denitrification of the nitrite thus produced. The production of methanol using autotrophic pathways is significant, since it also achieves biological carbon dioxide fixation. Consequently, the overall greenhouse footprints of wastewater treatment plants are reduced, i.e., by lowering both methane and carbon dioxide release as well as recovering methanol.
Methods and systems according to the disclosed subject matter can be used the conversion of any gaseous stream that contains methane with or without carbon dioxide and liquid streams containing ammonia to the biofuel, methanol, as well as other precursors of longer chain organic compounds (including alcohols and acids). Methods and systems according to the disclosed subject matter can be used to transform anaerobic digesters at wastewater treatment plants, landfills, peatbogs, and marshes, where production of methane is common, into biofuels and sources of biofuels, and thus converting them into biorefineries. Specifically, the methanol and longer chain organic acids and alcohols can be used for the following: 1. external carbon source for denitrification (market size ˜$50 million per year in the US alone); 2. Gasoline additives (Being done in large scale in China); 3. Pre-cursor for biodiesel production (biodiesel is one of the most rapidly growing fuels today); 4. Production of dimethylether (another biofuel); and 5. Precursor chemicals for chemical fuel cells. Methods and systems according to the disclosed subject matter allow for “biological” conversion of methane, a greenhouse gas, into a range of green fuels including methanol, DME and longer chain organic compounds. By using waste sources of methane, the reliance on natural gas is minimized. Waste processing facilities are converted to biorefineries.
Methods and systems according to the disclosed subject matter are completely biological, whereas the closest technologies are chemical. Methods and systems according to the disclosed subject matter also do not require clean methane and can be used to process digester gas, landfill gas, gas from peatbogs and marshes, without any cleaning or dehumidification. Methods and systems according to the disclosed subject matter are more cost effective than competing processes and require significantly less energy and resources for gas clean up. Transportation costs for the biofuels produced are also reduced for some industries such as wastewater treatment, since production is onsite at wastewater treatment plants and landfills.
Although the disclosed subject matter has been described and illustrated with respect to embodiments thereof, it should be understood by those skilled in the art that features of the disclosed embodiments can be combined, rearranged, etc., to produce additional embodiments within the scope of the invention, and that various other changes, omissions, and additions may be made therein and thereto, without parting from the spirit and scope of the present invention.
This application claims the benefit of U.S. Provisional Application No. 61/420,848, filed Dec. 8, 2011 and U.S. Provisional Application No. 61/546,278, filed Oct. 12, 2011, each of which is incorporated by reference as if disclosed herein in its entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US11/63911 | 12/8/2011 | WO | 00 | 12/17/2013 |
| Number | Date | Country | |
|---|---|---|---|
| 61420848 | Dec 2010 | US | |
| 61546278 | Oct 2011 | US |