System and Method of Increasing Methane Production in Anaerobic Digesters

US2022340464A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2022340464-A1
Application numberUS-202217726913-A
CountryUS
Kind codeA1
Filing dateApr 22, 2022
Priority dateApr 26, 2021
Publication dateOct 27, 2022
Grant date

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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A spore germination composition and method to produce a bioaugmentation solution that is added to an anaerobic digester or partially aerobic digester to increase biogas production. A nutrient-germinant composition comprises L-amino acids a phosphate buffer, an industrial preservative, and an optional source of potassium. The composition and spores of one or more Bacillus species are heated to a preferred elevated temperature range of 35° C. to 60° C. for an incubation period of around 20 to 60 minutes to form a bioaugmentation solution that is dispensed to the digester, preferably to the hydrolysis stage of the digester. A dose of bioaugmentation solution is added to the digester around once per day in an amount to provide at least 1000 CFU per mL of the full volume capacity of the digester, which can increase methane production by around 5 to 10% over operation of the digester without the bioaugmentation solution.

First claim

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We claim: 1 . A method of increasing methane production in a digester having a full volume capacity, the method comprising the following steps: heating a nutrient-spore composition to a temperature in a range of around 35° C. to 60° C. at or near a digester; maintaining the temperature of the nutrient-spore composition for an incubation period of around 20 to 60 minutes to form a bioaugmentation solution; dispensing a dose of the bioaugmentation solution to the digester; wherein the nutrient-spore composition comprises: (a) one or more L-amino acids, (b) one or more industrial preservatives, (c) one or more acids or salts of acids, (d) a thickener, and (e) bacteria; wherein the bacteria comprises one or more of Bacillus algicola, Bacillus amyloliquefaciens, Bacillus arseniciselenatis, Bacillus barbaricus, Bacillus circulans, Bacillus coagulans, Bacillus firmus, Bacillus jeotgali, Bacillus krulwichiae, Bacillus licheniformis, Bacillus mycoides, Bacillus mojavensis, Bacillus nealsonii, Bacillus novalis, Bacillus pseudomycoides, Bacillus safensis, Bacillus simplex, Bacillus smithii, Bacillus sonorensis, Bacillus subtilis, Bacillus thermoamylovorans, Bacillus vedderi, Bacillus vallismortis; Bacillus clausii, Bacillus lactis, Bacillus laterosporus, Bacillus laevolacticus, Bacillus lentus, Bacillus polymyxa, Bacillus pumilus, Bacillus megaterium, Bacillus sphaericus , or Bacillus toyonensis in spore form; and wherein the dose of bioaugmentation solution provides bacteria amounts of at least 1000 CFU per mL of the full volume capacity of the digester, even if the digester is operated at less than the full volume capacity. 2 . The method of claim 1 wherein the dose of bioaugmentation solution is dispensed to a hydrolysis stage of the digester. 3 . The method of claim 1 wherein the nutrient-spore composition comprises around 6 to 10% by weight of a nutrient-germinant composition and around 25 to 35% by weight of a spore composition, the method further comprising mixing the nutrient-germinant composition and the spore composition to form the nutrient-spore composition prior to or during the heating step; and wherein the nutrient-germinant composition comprises (1) around 8.9-133.5 g/L total of the one or more L-amino acids; (2) optionally around 7.4-55.8 g/L of potassium chloride; and (3) around 10-36 g/L monosodium phosphate, or around 30-90 g/L disodium phosphate, or around 15-61 g/L Tris base, or around 32.5-97.5 g/L HEPES, or a combination thereof; and wherein the spore composition is a liquid comprising (1) the one or more acids or salts of acids, (2) the thickener, and (3) a spore blend. 4 . The method of claim 3 wherein the spore blend is in a powdered form comprising 60 to 40% of the bacteria and 40 to 60% salt by weight of the spore blend. 5 . The method of claim 4 wherein the one or more acids or salts of acids comprises citric acid and wherein spore composition further comprises (1) around 75-125 g/L of the spore blend, (2) around 1.5-2.5 g/L of a first surfactant, (3) around 1.5-2.5 g/L of a second surfactant, (4) around 2.175-3.625 g/L of the thickener, (5) around 0.75-1.25 g/L of the citric acid, and (6) around 0.75-1.25 g/L of the one or more industrial preservatives. 6 . The method of claim 5 wherein the spore blend comprises at least around 2×10 11 CFUs/g of the bacteria. 7 . The method of claim 5 wherein the first surfactant is polysorbate 80 and the second surfactant is an amphoteric surfactant comprising cocamidopropyl betaine. 8 . The method of claim 7 wherein the thickener comprises xanthan gum. 9 . The method of claim 3 wherein the dose of bioaugmentation solution is dispensed to the hydrolysis stage of the digester and wherein the heating, maintaining, and dispensing steps are periodically repeated to form multiple doses of the bioaugmentation solution that are dispensed to the digester around once per 2 to 24 hours. 10 . The method of claim 9 wherein the digester is an anaerobic digester and the bacteria comprise one or more of Bacillus algicola, Bacillus amyloliquefaciens, Bacillus arseniciselenatis, Bacillus barbaricus, Bacillus circulans, Bacillus coagulans, Bacillus firmus, Bacillus jeotgali, Bacillus krulwichiae, Bacillus licheniformis, Bacillus mycoides, Bacillus mojavensis, Bacillus nealsonii, Bacillus novalis, Bacillus pseudomycoides, Bacillus safensis, Bacillus simplex, Bacillus smithii, Bacillus sonorensis, Bacillus subtilis, Bacillus thermoamylovorans, Bacillus vedderi , or Bacillus vallismortis in spore form and wherein the temperature range is around 38° C. to 50° C. 11 . The method of claim 9 wherein the digester is at least partially aerobic and the bacteria comprise one or more of Bacillus clausii, Bacillus lactis, Bacillus laterosporus, Bacillus laevolacticus, Bacillus lentus, Bacillus polymyxa, Bacillus pumilus, Bacillus megaterium, Bacillus sphaericus , or Bacillus toyonensis in spore form. 12 . The method of claim 3 wherein the nutrient-germinant composition is in a concentrated form and wherein the method further comprises diluting the nutrient-germinant composition to around 4-10% with water prior to or during the mixing step. 13 . The method of claim 1 wherein at least 80% of the bacteria in the bioaugmentation solution are in an activated state when the bioaugmentation solution is dispensed to the digester. 14 . The method of claim 1 wherein the one or more acids or salts of acids comprises citric acid; and wherein the nutrient-spore composition is in a concentrated form comprising (1) around 8.9-133.5 g/L each of the one or more L-amino acids, (2) around 0.8-3.3 g/L total of the one or more industrial preservatives, (3) around 1-5 g/L of the citric acid, (4) 10-30 g/L of a source of potassium, and (5) one or both of (a) around 29-117 g/L NaCl or (b) wherein the nutrient-spore composition has a pH of around 4.5-5.5. 15 . The method of claim 1 wherein the nutrient-spore composition further comprises a source of potassium chloride, monopotassium phosphate, dipotassium phosphate or a combination thereof. 16 . The method of claim 1 wherein the nutrient-spore composition (1) does not include any sources of nitrogen-hydrogen compounds, (2) does not include any chloride compounds other than sodium chloride or potassium chloride and (3) does not include any sugars. 17 . The method of claim 16 wherein the digester is an anaerobic digester and the bacteria comprise one or more of Bacillus subtilis, Bacillus licheniformis, Bacillus pumilus, Bacillus megaterium, Bacillus simplex , and Bacillus amyloliquefaciens. 18 . The method of claim 5 wherein at least 80% of the bacteria in the bioaugmentation solution are in an activated state when the bioaugmentation solution is dispensed to the digester; wherein the dose of bioaugmentation solution is dispensed to the hydrolysis stage of the digester; wherein the nutrient-spore composition does not include any (1) sources of nitrogen-hydrogen compounds, (2) chloride compounds other than sodium chloride or potassium chloride or (3) sugars; and wherein the digester is an anaerobic digester and the bacteria comprise one or more of Bacillus subtilis, Bacillus licheniformis, Bacillus pumilus, Bacillus megaterium, Bacillus simplex , and Bacillus amyloliquefaciens. 19 . The method of claim 5 wherein the nutrient-spore composition does not include any sources of nitrogen-hydrogen compounds. 20 . The method of claim 5 wherein the nutrient-spore composition does not includ

Assignees

Inventors

Classifications

  • Nutrients for stimulating the growth of microorganisms · CPC title

  • C02F11/04Primary

    Anaerobic treatment; Production of methane by such processes · CPC title

  • C02F3/348Primary

    characterised by the way or the form in which the microorganisms are added or dosed · CPC title

  • Consortia of bacteria · CPC title

  • Regulation methods for biological treatment · CPC title

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What does patent US2022340464A1 cover?
A spore germination composition and method to produce a bioaugmentation solution that is added to an anaerobic digester or partially aerobic digester to increase biogas production. A nutrient-germinant composition comprises L-amino acids a phosphate buffer, an industrial preservative, and an optional source of potassium. The composition and spores of one or more Bacillus species are heated to a…
Who is the assignee on this patent?
Nch Corp
What technology area does this patent fall under?
Primary CPC classification C02F11/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Oct 27 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).