Method for strengthening ammonia pretreatment of waste biomass by means of lignin-degrading bacteria
A technology for lignin degrading bacteria and waste biomass, which is applied in the directions of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., to achieve the effects of short treatment time, low cost and simple operation
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Embodiment 1
[0032] (1) The rice straw was crushed and sieved with 60 meshes, washed twice with ultrapure water, and dried at 60°C until constant weight.
[0033] (2) Put lignocellulose in a container of appropriate size, add ammonia solution with a concentration of 0.5% according to the solid-to-liquid ratio of 1:10 (g / ml), let it stand in a constant temperature environment of 160°C for 30 minutes, and then filter and separate to obtain Wet residue A.
[0034] (3) Rinse the wet residue A obtained by filtering and separating with distilled water repeatedly until the pH of the washing liquid is neutral, and dry at 60° C. to a constant weight to obtain dry residue B.
[0035] (4) Inoculate the Cupriavidus basilensis B-8 bacteria stored on the LB solid plate in the LB liquid medium, and culture at 30°C for 18 hours (the optical density at 600nm reaches 0.8-1.0) to obtain Cupriavidus basilensis B-8 The seed liquid of the LB solid culture medium wherein said LB solid medium each composition ra...
Embodiment 2
[0042] (1) The rice straw was crushed and sieved with 60 meshes, washed twice with ultrapure water, and dried at 60°C until constant weight.
[0043] (2) Further place lignocellulose in a container of appropriate size, add ammonia solution with a concentration of 0.5% according to the solid-liquid ratio of 1:10 (g / ml), and stand in a constant temperature environment of 180°C for 30 minutes, then filter and separate Wet slag A was obtained.
[0044] (3) Rinse the wet residue A obtained by filtering and separating with distilled water repeatedly until the pH of the washing liquid is neutral, and dry at 60° C. to a constant weight to obtain dry residue B.
[0045] (4) Inoculate the Cupriavidus basilensisB-8 thalline preserved on the LB solid plate in the LB liquid medium, and cultivate it for 18h at a temperature of 30°C (the optical density at 600nm reaches 0.8-1.0) to obtain Cupriavidus basilensisB-8 Seed liquid; wherein the proportion of each component of the LB solid medium ...
Embodiment 3
[0052] (1) The rice straw was crushed and sieved with 60 meshes, washed twice with ultrapure water, and dried at 60°C until constant weight.
[0053] (2) Put lignocellulose in a container of appropriate size, add ammonia solution with a concentration of 0.5% according to the solid-to-liquid ratio of 1:10 (g / ml), and place it in a constant temperature environment of 200°C for 30 minutes, then filter and separate to obtain Wet residue A.
[0054] (3) Rinse the wet residue A obtained by filtering and separating with distilled water repeatedly until the pH of the washing liquid is neutral, and dry at 60° C. to a constant weight to obtain dry residue B.
[0055] (4) Inoculate the Cupriavidus basilensisB-8 thalline preserved on the LB solid plate in the LB liquid medium, and cultivate it for 18h at a temperature of 30°C (the optical density at 600nm reaches 0.8-1.0) to obtain Cupriavidus basilensisB-8 Seed liquid; wherein the proportion of each component of the LB solid medium is: ...
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