SOLARGAS SYSTEM OPERATED IN MULTIPLE MODES
20180187233 ยท 2018-07-05
Assignee
Inventors
- David FEUSTEL (Berlin, DE)
- Benjamin HERZOG (Berlin, DE)
- Johann BAUERFEIND (Berlin, DE)
- Yannick BOLDT (Berlin, DE)
Cpc classification
C12M29/04
CHEMISTRY; METALLURGY
C12M29/18
CHEMISTRY; METALLURGY
Y02E50/30
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
International classification
C12P39/00
CHEMISTRY; METALLURGY
C12M1/107
CHEMISTRY; METALLURGY
Abstract
The invention relates to a method and a device for producing biogas in a combined fermenter, in the first section (2) of which organic material is produced by phototrophic microorganisms (1) using atmospheric carbon dioxide and oxygen, said organic material being used to produce biomethane by means of methanogens (5) in a second section (4). The fermenter is operated in multiple modes and using special gassing and degassing methods such that an optimal gas supply corresponding to the requirements of the respective microorganisms and preferably also the absorption or the use of atmospheric carbon dioxide is ensured.
Claims
1. A method for producing biogas in a combined fermenter, in which phototrophic microorganisms (1) in a first section (2) produce organic material, in particular glycolic acid from carbon dioxide and oxygen, and secrete it into a medium (3) (production mode) which is fed into a second section (4) in which methanogens (5) produce biomethane and carbon dioxide therefrom under anoxic conditions, characterized in that the medium (3) is degassed to remove oxygen during the transition from the first section (2) to the second section (4) and is regassed with oxygen during return (exchange mode).
2. The method according to claim 1, characterized in that, while contact to the second section (4) is interrupted, the medium (3) is degassed to remove oxygen and is gassed with air from the environment during return; the air is then used by the phototrophic microorganisms (1) for carbon assimilation (regeneration mode); the medium (3) is then degassed to remove air and gassed with oxygen during return.
3. The method according to claim 1 or 2, characterized in that the ratio of carbon dioxide to oxygen in the medium (3) located in the first section (2) is low, preferably 1:800 to 1:3000, in the production mode.
4. The method according to any one of the preceding claims, characterized in that, in the exchange mode, the medium (3) is gassed with a substitute gas, in particular with carbon dioxide or nitrogen, after the oxygen degassing during the transition from the first section (2) to the second section (4), and is degassed to remove the substitute gas during return before the oxygen gassing.
5. The method according to any one of the preceding claims, characterized in that the carbon dioxide is separated from the biogas produced in the second section (4) and is used for carbon dioxide gassing according to claim 4.
6. The method according to any one of the preceding claims, characterized in that filters, in particular hollow fiber contactors, are used for the gassing and degassing, the pore size being less than 0.1 m, preferably less than 0.04 m.
7. The method according to any one of the preceding claims, characterized in that cyanobacteria, preferably biofilm-forming and preferably metabolizing the produced organic material minimally, more preferably less than 10% thereof, in particular Gloeothece 6909, Plectonema boryanum, Anabaena sp. and Nostoc sp., are present as the phototrophic microorganisms (1) in the first section (2).
8. The method according to any one of the preceding claims, characterized in that the methanogens (5) in the second section (4) are a mixture of acetotrophic and hydrogenotrophic archaea, wherein the acetotrophic archaea, in particular Methanosarcina or Synthrophobotulus, split the organic material from the first section (2) into carbon dioxide and hydrogen which is used by hydrogenotrophic archaea, in particular Methanocella paludicola, Methanocella arvoryzae or Methanopyrus kandleri, for biomethane production, and/or are mixed cultures obtained by selection from sediments of lakes and oceans, bovine rumen, intestines of termites and other animals, rice fields, marshes or biogas systems.
9. The method according to any one of the preceding claims, characterized in that inhibitors of intracellular degradation of the organic material and/or intracellular carbon dioxide storage are present in the first section (2).
10. The method according to any one of the preceding claims, characterized in that, in the phototrophic microorganisms (1), the expression and/or the activity of glycolic acid dehydrogenase and/or glycolic acid oxidase are or are being suppressed; carbon dioxide accumulation by carboxysomes and pyrenoids is inhibited; ribulose-1,5-bisphosphate carboxylase/oxygenase and/or glycolic acid phosphate phosphatase are overexpressed; ribulose-1,5-bisphosphate carboxylase/oxygenase type II is expressed; the excretion of organic material, especially of glycolic acid, through the cell membrane is enhanced.
11. A device for producing biogas in a combined fermenter, comprising the following components: a first section (2), which is partially transparent, with phototrophic microorganisms (1) located in a medium (3); a second section (4), which is opaque, with methanogens (5) located in the medium (3) which is exchanged in exchange mode with the first section (2), the oxygen content being reduced; a connecting system (6) between the first section (2) and the second section (4); filters in the connecting system (6) for gassing and degassing the medium (3) which are connected to gas feeds and gas discharges, a biogas discharge (7) from the second section (4); pumps and valves for distributing liquid and gas streams.
12. The device according to claim 11, characterized in that the connecting system (6) comprises a first connecting pipe (8) and a second connecting pipe (9); the connecting system (6) comprises a first cross-connecting pipe (10), interconnecting the first connecting pipe (8) and the second connecting pipe (9); a first filter (11) is a part of the first connecting pipe (8) between the first section (2) and the first cross-connecting pipe (10); a second filter (12) is a part of the second connecting pipe (9) between the first section (2) and the first cross-connecting pipe (10); a third filter (13) is a part of the first connecting pipe (8) between the second section (4) and the first cross-connecting pipe (10); a fourth filter (14) is a part of the second connecting pipe (9) between the second section (4) and the first cross-connecting pipe (10); a second cross-connecting pipe (15) connecting the first section (2) and the first cross-connecting pipe (10); a fifth filter (16) is a part of the second cross-connecting pipe (15) and is connected to an air line (17) with an air filter (18), preferably with a pore size of 0.2 m or less; an oxygen discharge (19), an oxygen feed (20), a substitute gas feed (21) and a substitute gas discharge (22) are present; a substitute gas storage (23) and an oxygen storage (24) are present; a biogas filter (25) is provided as a part of the biogas discharge (7) with a downstream biomethane storage tank (26); the substitute gas storage (23) is connected to the biogas filter (25); a first pump (27) is present as a part of the first cross-connecting pipe (8) between the first section (2) and the first filter (11) and a second pump (28) is present as a part of the second connecting pipe (9) between the first cross-connecting pipe (10) and the second filter (12).
13. The device according to any one of the preceding claims, characterized in that the first section (2) is protected from excessive solar irradiation, in particular that the transparent region (29) of the first section (2) can be gradually darkened.
14. The device according to any one of the preceding claims, characterized in that the phototrophic microorganisms (1) are preferably immobilized on cellulose or a mobile carrier material, in particular gas-permeable gel capsules, and the methanogens (5) are preferably immobilized on activated carbon or a mobile carrier material, in particular gas-permeable gel capsules.
15. The device according to any one of the preceding claims, characterized in that the filters are configured as hollow fiber contactors, in particular having a gas pump (30), a permeate space (31), partitions (32), hollow fibers (33), an inlet space (34) and an outlet space (35).
Description
DESCRIPTION OF THE DRAWINGS
[0042]
[0043]
[0044]
[0045]
[0046]
[0047]
[0048]
DESCRIPTION OF AN EXEMPLARY EMBODIMENT
[0049] In the production mode shown in
[0050] In the exchange mode shown in
[0051] In the transition to the regeneration mode, the valves from the second section (4), a part of the first connecting pipe (8), from the second connecting part (9) and a part of the first cross-connecting pipe (10) are closed according to
[0052] In the regeneration mode, the valves of the sections towards the connecting system (6), as shown in
[0053] In the transition to the production mode, the vales from the second section (4), the first connecting pipe (8), a part of the second connecting pipe (9) and a part of the first cross-connecting pipe (1) are closed according to
[0054] The following non-patent literature has been cited: [0055] Barber, J. 2009Photosynthetic energy conversion: natural and artificial, Chemical Society Reviews 2009 (38), pp. 185-196 [0056] Bauwe, H. 2011Photorespiration: The Bridge to C4 Photosynthesis. In: Agepati S. Raghavendra (ed.) and Rowan F. Sage (ed.): C4 Photosynthesis and Related CO2 Concentrated Mechanisms (Advances in Photosynthesis and Respiration), Springer Netherlands 2011, pp. 81-108 [0057] FHI report of 2011Algennachhaltige Rohstoffquelle fr Wertstoffe und Energie, Fraunhofer Institut fr Grenzflchenund Bioverfahrenstechnik 2011, p. 2 [0058] Bernacchi, S. et al. 2014Process efficiency simulation for key process parameters in biological methanogenesis, AIMS Bioeng. 2014 (1), pp. 53-71 [0059] Blankenship, R. E. et al. 2011Comparing Photosynthetic and Photovoltaic Efficiencies and Recognizing the Potential for Improvement, Science 2011 (332), pp. 805-809 [0060] Carrieri, D. et al. 2015Enhancing photo-catalytic production of organic acids in the cyanobacterium Synechocystis sp. PCC 6803 glgC, a strain incapable of glycogen storage, Microb. Biotechnol. 2015 (8), pp. 275-280 [0061] Dismukes, G. C. et al. 2008Aquatic Phototrophs: efficient alternatives to land-based crops for fuels, Current Opinion in Biotechnology 2008 (19), pp. 235-240 [0062] Doravari, S. et al. 1980Effect of butyl 2-hydroxy-3-butynoate on sunflower leaf photosynthesis and photorespiration, Plant Physiol. 1980 (66), pp. 628-631 [0063] Edenborn, H. M. et al. 1985Glycolate metabolism by Pseudomonas sp., strain S227, isolated from a coastal marine sediment, Marine Biology (88), pp. 199-205 [0064] Egli, C. et al. 1989Monochloro- and dichloroacetic acids as carbon and energy sources for a stable, methanogenic mixed culture, Arch. Microbiol. 1989 (152), pp. 218-223 [0065] Fachverband Biogas PrognoseBranchenzahlenprognose fr die Jahre 2014 and 2015, Fachverband Biogas e. V., June 2014, p. 2 [0066] Friedrich, M. et al. 1991Fermentative degradation of glycolic acid by defined syntrophic cocultures, Arch. of Microbiol. 1991 (156), pp. 398-404 [0067] Friedrich, M. et al. 1996Phylogenetic Positions of Desulfofustis glycolicus gen. nov., sp. nov., and Synthrobotulus glycolicus gen. nov., sp. nov., Two New Strict Anaerobes Growing with Glycolic Acid, Int. J. of Sys. Bact., 1996, pp. 1065-1069 [0068] Gnther, A. et al. 2012Methane production from glycolate excreting algae as a new concept in the production of biofuels, Biores. Tech. 2012 (121), pp. 454-457 [0069] Kurz, W. G. W. et al. 1973Metabolism of glycolic acid by Azotobacter chroococcum PRL H62, Can. J. of Microbiol. 1973 (19), pp. 321-324 [0070] Latifi, A. et al. 2009Oxidative stress in cyanobacteria, FEMS Microbiol. Rev. 2009 (33), pp. 258-278 [0071] Linder, H. 1998Biologie, Schroedel, 21.sup.st ed., 1998, p. 43 [0072] Lorimer, G. H. 1981The carboxylation and oxygenation of ribulose 1,5-bisphosphate; The primary events in photosynthesis and photorespiration. Ann. Rev. Plant Physiol. 1981 (32), pp. 349-383 [0073] MacColl, R. 1998Cyanobacterial phycobilisomes, J. Struct. Biol. 1998 (15), pp. 311-334 [0074] Masukawa, H. et al. 2012Genetic Engineering of Cyanobacteria to Enhance Biohydrogen Production from Sunlight and Water, AMBIO 2012 (41), pp. 169-173 [0075] Miller, A. G. et al. 1989Glycolaldehyde Inhibits CO2 Fixation in the Cyanobacterium Synechococcus UTEX 625 without Inhibiting the Accumulation of Inorganic Carbon or the Associated Quenching of Chlorophyll a Fluorescence, Plant Phys. 1989 (91), pp. 1044-1049 [0076] Moroney, J. V. et al. 1986Glycolate metabolism and excretion by Chlamydomonas reinhardtii, Plant Physiol. 1986 (82), S. 821-826 [0077] Moroney, J. V. et al. 2001Carbonic anhydrases in plants and algae, Plant, Cell & Env. 2001 (24), pp. 141-153 [0078] Nabors, M. W. et al. 2007Botanik, Pearson Studium, 1.sup.st ed., 2007, pp. 221-222 [0079] Renstrm, E. et al. 1989Glycolate metabolism in cyanobacteria. I. Glycolate excretion and phosphoglycolate phosphatase activity, Phys. Plant. 1989 (43), pp. 137-143 [0080] Sari, S. 2010Untersuchung der Dehydrogenierung von NADH/NADPH in isolierten und gereinigten Membranen von drei verschiedenen Cyanobakterienspezies, die in zwei verschiedenen Bedingungen gezchtet wurden, Diplomarbeit, University of Vienna, 2010, p. 8 [0081] Schwab, M. 2007Biogasertrge aus EnergiepflanzenEine kritische Bewertung des Datenpotentials, Kuratorium fr Technik und Bauwesen in der Landwirtschaft e. V. 2007, p. 4 [0082] Stein, J. 1973Handbook of Phycological methods. Culture methods and growth measurements. Cambr. Univ. Press. 1973, pp. 448 et seqq. [0083] Stenberg, K. 1997Three-dimensional structures of glycolate oxidase with bound active-site inhibitors, Prot. Sc. 1997 (6), pp. 1009-1015 [0084] Zelitch, I. 1966Increased Rate of Net Photosynthetic Carbon Dioxide Uptake Caused by the Inhibition of Glycolate Oxidase, Plant Physiol. 1966 (41), pp. 1623-1631