BIOLOGICAL AND CHEMICAL PROCESS UTILIZING CHEMOAUTOTROPHIC MICROORGANISMS FOR THE CHEMOSYTHETIC FIXATION OF CARBON DIOXIDE AND/OR OTHER INORGANIC CARBON SOURCES INTO ORGANIC COMPOUNDS, AND THE GENERATION OF ADDITIONAL USEFUL PRODUCTS

• US 20130078690A1
• Filed: 05/12/2010
• Published: 03/28/2013
• Est. Priority Date: 11/06/2008
• Status: Abandoned Application

• Current Assignee: Kiverdi, Inc.
• Original Assignee: Kiverdi, Inc.
• Inventors: Reed, John S.
• Application Number:
  US13/508,472
• Publication Number:
  US 20130078690A1
• Time in Patent Office: Days
• US Class Current: 435/140
• CPC Class Codes: C12N 1/20 Bacteria; Culture media therefor
• CPC Class Codes: C12P 1/04 by using bacteria
• CPC Class Codes: C12P 3/00 Preparation of elements or inorganic compounds except carbon dioxide recovery of carbon dioxides as by-products C12F3/02
• CPC Class Codes: C12P 5/023 Methane
• CPC Class Codes: C12P 7/065 with microorganisms other than yeasts
• CPC Class Codes: C12P 7/08 produced as by-product or from waste or cellulosic material substrate
• CPC Class Codes: C12P 7/16 Butanols
• CPC Class Codes: C12P 7/40 containing a carboxyl group including Peroxycarboxylic acids
• CPC Class Codes: C12P 7/54 Acetic acid vinegar C12J
• CPC Class Codes: C12P 7/649 Biodiesel, i.e. fatty acid alkyl esters
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel
• CPC Class Codes: Y02E 50/30 Fuel from waste, e.g. synthetic alcohol or diesel

Abstract

The invention described herein presents compositions and methods for a multistep biological and chemical process for the capture and conversion of carbon dioxide and/or other forms of inorganic carbon into organic chemicals including biofuels or other useful industrial, chemical, pharmaceutical, or biomass products. One or more process steps utilizes chemoautotrophic microorganisms to fix inorganic carbon into organic compounds through chemosynthesis. An additional feature described are process steps whereby electron donors used for the chemosynthetic fixation of carbon are generated by chemical or electrochemical means, or are produced from inorganic or waste sources. An additional feature described are process steps for the recovery of useful chemicals produced by the carbon dioxide capture and conversion process, both from chemosynthetic reaction steps, as well as from non-biological reaction steps.

Claims

1. A biological and chemical process for the capture and conversion of carbon dioxide and/or other sources of inorganic carbon, into organic compounds, comprising:

introducing carbon dioxide gas, either alone and/or dissolved in a mixture or solution further comprising carbonate ion and/or bicarbonate ion, and/or introducing inorganic carbon contained in a solid phase into an environment suitable for maintaining chemoautotrophic organisms and/or chemoautotroph cell extracts; and

fixing the carbon dioxide and/or inorganic carbon into organic compounds within the environment via at least one chemosynthetic carbon fixing reaction utilizing obligate and/or facultative chemoautotrophic microorganisms and/or cell extracts containing enzymes from chemoautotrophic microorganisms;

wherein where the chemosynthetic carbon fixing reaction is driven by chemical and/or electrochemical energy provided by electron donors and electron acceptors that have been generated chemically and/or electrochemically and/or or are introduced into the environment from at least one source external to the environment.

2. A method according to claim 1, whereby said electron donors include but are not limited to one or more of the following reducing agents:

ammonia;

ammonium;

carbon monoxide;

dithionite;

elemental sulfur;

hydrocarbons;

hydrogen;

metabisulfites;

nitric oxide;

nitrites;

sulfates such as thiosulfates including but not limited to sodium thiosulfate (Na₂S₂O₃) or calcium thiosulfate (CaS₂O₃);

sulfides such as hydrogen sulfide;

sulfites;

thionate;

thionite;

transition metals or their sulfides, oxides, chalcogenides, halides, hydroxides, oxyhydroxides, phosphates, sulfates, or carbonates, in dissolved or solid phases; and

conduction or valence band electrons in solid state electrode materials.

3. A method according to claim 1, whereby said electron acceptors comprise one or more of the following:

carbon dioxide;

oxygen;

nitrites;

nitrates;

ferric iron or other transition metal ions;

sulfates;

or valence or conduction band holes in solid state electrode materials.

4. A method according to claim 1, wherein the fixing step is proceeded by one or more chemical preprocessing steps in which said electron donors and/or said electron acceptors are generated and/or refined from at least one input chemical and/or are recycled from chemicals produced during the fixing step and/or chemicals derived from waste streams from other industrial, mining, agricultural, sewage or waste generating processes.

5. A method according to claim 1, wherein fixing step is followed by one or more process steps in which organic and/or inorganic chemical products of chemosynthesis are separated from a process stream produced during the fixing step and processed to form products in a form suitable for storage, shipping, and sale;

as well as one or more process steps in which cell mass is separated from the process stream and recycled to the environment as and/or collected and processed to produce biomass in a form suitable for storage, shipping, and sale.

6. A method according to claim 1, wherein the fixing step is followed by one or more process steps in which waste products and/or impurities or contaminants are removed from a process stream produced during the fixing step and disposed of.

7. A method according to claim 1, wherein the fixing step is followed by one or more process steps in which any unused nutrients and/or process water left after removal of chemoautotrophic cell mass and/or chemical co-products of chemosynthesis and/or waste products or contaminants of the process stream produced during the fixing step are recycled back into the environment to support further chemosynthesis.

8. A method according to claim 1, wherein the obligate and/or facultative chemoautotrophic microorganisms include one or more of the following:

Acetoanaerobium sp.;

Acetobacterium sp.;

Acetogenium sp.;

Achromobacter sp.;

Acidianus sp.;

Acinetobacter sp.;

Actinomadura sp.;

Aeromonas sp.;

Alcaligenes sp.;

Alcaligenes sp.;

Arcobacter sp.;

Aureobacterium sp.;

Bacillus sp.;

Beggiatoa sp.;

Butyribacterium sp.;

Carboxydothermus sp.;

Clostridium sp.;

Comamonas sp.;

Dehalobacter sp.;

Dehalococcoide sp.;

Dehalospirillum sp.;

Desulfobacterium sp.;

Desulfomonile sp.;

Desulfotomaculum sp.;

Desulfovibrio sp.;

Desulfurosarcina sp.;

Ectothiorhodospira sp.;

Enterobacter sp.;

Eubacterium sp.;

Ferroplasma sp.;

Halothibacillus sp.;

Hydrogenobacter sp.;

Hydrogenomonas sp.;

Leptospirillum sp.;

Metallosphaera sp.;

Methanobacterium sp.;

Methanobrevibacter sp.;

Methanococcus sp.;

Methanosarcina sp.;

Micrococcus sp.;

Nitrobacter sp.;

Nitrosococcus sp.;

Nitrosolobus sp.;

Nitrosomonas sp.;

Nitrosospira sp.;

Nitrosovibrio sp.;

Nitrospina sp.;

Oleomonas sp.;

Paracoccus sp.;

Peptostreptococcus sp.;

Planctomycetes sp.;

Pseudomonas sp.;

Ralstonia sp.;

Rhodobacter sp.;

Rhodococcus sp.;

Rhodocyclus sp.;

Rhodomicrobium sp.;

Rhodopseudomonas sp.;

Rhodospirillum sp.;

Shewanella sp.;

Streptomyces sp.;

Sulfobacillus sp.;

Sulfolobus sp.;

Thiobacillus sp.;

Thiomicrospira sp.;

Thioploca sp.;

Thiosphaera sp.;

Thiothrix sp.;

sulfur-oxidizers;

hydrogen-oxidizers;

iron-oxidizers;

acetogens; and

methanogens;

consortiums of microorganisms that include chemoautotrophs;

chemoautotrophs native to at least one of hydrothermal vents, geothermal vents, hot springs, cold seeps, underground aquifers, salt lakes, saline formations, mines, acid mine drainage, mine tailings, oil wells, refinery wastewater. Coal seams, deep sub-surface;

waste water and sewage treatment plants;

geothermal power plants, sulfatara fields, and soils; and

extremophiles selected from one or more of thermophiles, hyperthermophiles, acidophiles, halophiles, and psychrophiles.

9. A method according to claim 1, wherein said electron donors and/or electron acceptors are generated or recycled using renewable, alternative, or conventional sources of power that are low in greenhouse gas emissions, and wherein said sources of power are selected from at least one of photovoltaics, solar thermal, wind power, hydroelectric, nuclear, geothermal, enhanced geothermal, ocean thermal, ocean wave power, and tidal power.

10. A method according to claim 1, wherein molecular hydrogen acts as an electron donor and is generated through electrolysis of water via a method using at least one of Proton Exchange Membranes (PEM), a liquid electrolytes, high-pressure electrolysis, high temperature electrolysis of steam (HTES);

thermochemical splitting of water via a method using the iron oxide cycle, cerium(IV) oxide-cerium(III) oxide cycle, zinc zinc-oxide cycle, sulfur-iodine cycle, copper-chlorine cycle, calcium-bromine-iron cycle, hybrid sulfur cycle;

electrolysis of hydrogen sulfide;

thermochemical splitting of hydrogen sulfide;

a electrochemical or thermochemical processes known to produce hydrogen with low- or no-carbon dioxide emissions comprising at least one of carbon capture and sequestration enabled methane reforming, carbon capture and sequestration enabled coal gasification, the Kvæ

rner-process and other processes generating a carbon-black product, carbon capture and sequestration enabled gasification or pyrolysis of biomass; and

the half-cell reduction of H⁺ to H₂ accompanied by the half-cell oxidization of electron sources comprising ferrous iron (Fe²⁺) oxidized to ferric iron (Fe³⁺) and/or the oxidation of sulfur compounds wherein the oxidized iron or sulfur is recycled to back to a reduced state through additional chemical reactions with minerals comprising at least one of metal sulfides, hydrogen sulfide, and hydrocarbons.

11. A method according to claim 1, wherein said electron donors are generated from minerals of natural origin selected from one or more of the following:

elemental Fe⁰;

siderite (FeCO₃);

magnetite (Fe₃O₄);

pyrite or marcasite (FeS₂), pyrrhotite (Fe_(1-x)S (x=0 to 0.2), pentlandite (Fe,Ni)₉S₈, violarite (Ni₂FeS₄), bravoite (Ni,Fe)S₂, arsenopyrite (FeAsS), or other iron sulfides;

realgar (AsS);

orpiment (As₂S₃);

cobaltite (CoAsS);

rhodochrosite (MnCO₃);

chalcopyrite (CuFeS₂), bornite (Cu₅FeS₄), covellite (CuS), tetrahedrite (Cu₈Sb₂S₇), enargite (Cu₃AsS₄), tennantite (C₁₂As₄.S₁₃), chalcocite (Cu₂S), or other copper sulfides;

sphalerite (ZnS), marmatite (ZnS), or other zinc sulfides;

galena (PbS), geocronite (Pb₅(Sb,As₂)S₈), or other lead sulfides;

argentite or acanthite (Ag₂S);

molybdenite (MoS₂);

millerite (NiS), polydymite (Ni₃S₄) or other nickel sulfides;

antimonite (Sb₂S₃);

Ga₂S₃;

CuSe;

cooperite (PtS);

laurite (RuS₂);

braggite (Pt,Pd,Ni)S;

FeCl₂.

12. A method according to claim 1, wherein said electron donors are generated from pollutants or waste products selected from one or more of the following:

process gas;

tail gas;

enhanced oil recovery vent gas;

biogas;

acid mine drainage;

landfill leachate;

landfill gas;

geothermal gas;

geothermal sludge or brine;

metal contaminants;

gangue;

tailings;

sulfides;

disulfides;

mercaptans selected from one or more of methyl and dimethyl mercaptan and ethyl mercaptan;

carbonyl sulfide;

carbon disulfide;

alkanesulfonates;

dialkyl sulfides;

thiosulfate;

thiofurans;

thiocyanates;

isothiocyanates;

thioureas;

thiols;

thiophenols;

thioethers;

thiophene;

dibenzothiophene;

tetrathionate;

dithionite;

thionate;

dialkyl disulfides;

sulfones;

sulfoxides;

sulfolanes;

sulfonic acid;

dimethylsulfoniopropionate;

sulfonic esters;

hydrogen sulfide;

sulfate esters;

organic sulfur;

sulfur dioxide and all other sour gases.

13. A method according to claim 1, wherein delivery of reducing equivalents from the said electron donors to the chemoautotrophs for the said chemosynthetic reaction or reactions during the fixing step is kinetically and/or thermodynamically enhanced by one or more of introduction of hydrogen storage materials into the environment in the form of a solid support media for microbial growth that facilitates bringing absorbed or adsorbed hydrogen electron donors into close proximity with the chemoautotrophic organisms;

introduction of electron mediators selected from one or more of cytochromes, formate, methyl-viologen, NAD⁺/NADH, neutral red (NR), and quinones to help transfer reducing power from poorly soluble electron donor comprising H₂ gas or electrons in solid state electrode materials into the chemoautotrophic culture media; and

introduction of electrode materials in the form of a solid growth support media directly into the environment that facilitates bringing solid state electrons into close proximity with the chemoautotrophic organisms.

14. A method according to claim 1, wherein said electron donors are generated within or recycled to the environment through non- or low-carbon dioxide emitting chemical reactions with hydrocarbons selected from one or more of thermochemical reduction of sulfate reaction (TSR) and the Muller-Kuhne reaction for the production of hydrogen sulfide or reduced sulfur;

and methane reforming-like reactions utilizing metal oxides in place of water, the metal oxides selected from one or more of iron oxide, calcium oxide, and magnesium oxide; and

wherein the hydrocarbon is reacted to form solid carbonate with little or no emissions of carbon dioxide gas along with hydrogen electron donor product.

15. A method according to claim 1, wherein said at least one chemosynthetic reaction is performed by chemoautotrophic microorganisms that have been improved, optimized or engineered for the fixation of carbon dioxide and/or other forms of inorganic carbon and the production of organic compounds through methods including one or more of the following:

accelerated mutagenesis, genetic engineering or modification, hybridization, synthetic biology and traditional selective breeding.

16. A method according to claim 1, wherein said at least one chemosynthetic reaction results in the formation of chemicals including at least one of acetic acid, other organic acids and salts of organic acids, ethanol, butanol, methane, hydrogen, hydrocarbons, sulfuric acid, sulfate salts, elemental sulfur, sulfides, nitrates, ferric iron and other transition metal ions, other salts, acids and bases.

17. A method according to claim 1, wherein organic and/or inorganic chemical products are recovered from chemoautotrophic growth medium of the at least one chemosynthetic reaction, and wherein the organic and/or inorganic chemical products are useful as biofuels or as feedstock for biofuel production;

in the production of fertilizers;

as leaching agents for the chemical extraction of metals in mining or bioremediation, and/or as chemicals reagents in industrial or mining processes.

18. A method according to claim 1, wherein biomass and/or biochemicals are produced by the at least one chemosynthetic reaction, and wherein the biomass and/or biochemicals are useful as a biomass fuel for combustion;

as a fuel to be co-fired with fossil fuels;

as a carbon source for large scale fermentations to produce at least one of commercial enzymes, antibiotics, amino acids, vitamins, bioplastics, glycerol, and 1,3-propanediol;

as a nutrient source for the growth of other microbes or organisms;

as feed for animals selected from cattle, sheep, chickens, pigs, and/or fish;

as feed stock for alcohol or other biofuel fermentation and/or gasification and liquefaction processes comprising direct liquefaction, Fisher Tropsch processes, methanol synthesis, pyrolysis, transesterification, or microbial syngas conversions for the production of liquid fuel;

as feed stock for methane or biogas production;

as fertilizer;

as raw material for manufacturing or chemical processes;

as sources of pharmaceutical, medicinal or nutritional substances; and

as soil additives and soil stabilizers.

19. A method according to claim 1, wherein cultures of said chemoautotrophic organisms are maintained the environment, which environment comprises and/or is formed at least in part by a microbial culture apparatus selected from:

airlift reactors;

biological scrubber columns;

bioreactors;

bubble columns;

continuous stirred tank reactors;

counter-current, upflow, expanded-bed reactors;

digesters;

sewage and/or waste water treatment or bioremediation systems;

one or more filters selected from trickling filters, rotating biological contactor filters, rotating discs, and soil filters;

fluidized bed reactors;

gas lift fermenters;

immobilized cell reactors;

membrane biofilm reactors;

mine shafts;

pachuca tanks;

packed-bed reactors;

plug-flow reactors;

static mixers;

tanks;

trickle bed reactors;

vats;

vertical shaft bioreactors;

wells;

caverns;

caves;

cisterns;

lagoons;

ponds;

pools;

quarries;

reservoirs; and

towers.

20. A method according to claim 1, further comprising reacting carbon dioxide with minerals to form a carbonate or bicarbonate product.

21. A method according to claim 1, wherein carbon dioxide is introduced in the introducing step, and wherein the carbon dioxide is dissolved in an aqueous solution.

22. A method according to claim 21, wherein the aqueous solution comprises seawater.

23. A method according to claim 1, wherein a solid phase inorganic carbon compound is introduced in the introducing step, and wherein the inorganic carbon compound is a carbonate mineral.

24. A method according to claim 19, wherein the apparatus comprises a vessel having a base, siding, walls, lining, and top, at least one of the base, siding, walls, lining, and top being constructed out of bitumen, cement, ceramics, clay, concrete, epoxy, fiberglass, glass, macadam, plastics, sand, sealant, soil, steels;

non-steel metals;

metal alloys, stone, tar, wood, and combinations thereof.

25. A method according to claim 1, wherein the electron donors and/or electron acceptors are introduced into the environment from at least one inorganic source or waste source.

26. A method according to claim 20, wherein the minerals comprise oxides or hydroxides.