Preparing method of compound microorganism agent for papermaking wastewater
A technology of composite microbial bacterial agent and papermaking wastewater, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve problems such as dark black liquor, polluted water sources, health and environmental hazards, and achieve promising prospects Effect
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Embodiment 1
[0044] Step 1. Activate and expand each strain:
[0045] Firstly, Trametes yunzhi, Phanerochaete chrysosporium, Bacillus subtilis, Bacillus pumilus and Pseudomonas alcaligenes were activated on the solid medium plate; then, the liquid medium of each strain was added to different In the Erlenmeyer flask, connect the single colonies on each solid medium to the corresponding Erlenmeyer flask, and cultivate at 28-30℃ until the bacterial cell content in each Erlenmeyer flask reaches 1.0×10 8 -1.0×10 9 Pcs / mL; then add the liquid culture medium of each strain into different fermenters, and connect the bacteria in the triangular flask to the corresponding fermentor, and cultivate the bacteria in each fermentor at 28-30℃ Body content reaches 1.0×10 8 -1.0×10 9 Pcs / mL;
[0046] Step 2. Centrifugal separation and drying to obtain the microbial powder:
[0047] Centrifugal separation of the microbial bacteria liquid obtained by the expansion of the fermenter in step 1, collect the precipitate ...
Embodiment 2
[0051] Step 1. Activate and expand each strain:
[0052] Firstly, Trametes yunzhi, Phanerochaete chrysosporium, Bacillus subtilis, Bacillus pumilus and Pseudomonas alcaligenes were activated on the solid medium plate; then, the liquid medium of each strain was added to different In the Erlenmeyer flask, connect the single colonies on each solid medium to the corresponding Erlenmeyer flask, and cultivate at 28-30℃ until the bacterial cell content in each Erlenmeyer flask reaches 1.0×10 8 -1.0×10 9 Pcs / mL; then add the liquid culture medium of each strain into different fermenters, and connect the bacteria in the triangular flask to the corresponding fermentor, and cultivate the bacteria in each fermentor at 28-30℃ Body content reaches 1.0×10 8 -1.0×10 9 Pcs / mL;
[0053] Step 2. Centrifugal separation and drying to obtain the microbial powder:
[0054] After centrifugal separation of the microbial bacteria liquid obtained by the expansion of the fermentor in step 1, the collected sedi...
Embodiment 3
[0058] Step 1. Activate and expand each strain:
[0059] Firstly, Trametes yunzhi, Phanerochaete chrysosporium, Bacillus subtilis, Bacillus pumilus and Pseudomonas alcaligenes were activated on the solid medium plate; then, the liquid medium of each strain was added to different In the Erlenmeyer flask, connect the single colonies on each solid medium to the corresponding Erlenmeyer flask, and cultivate at 28-30℃ until the bacterial cell content in each Erlenmeyer flask reaches 1.0×10 8 -1.0×10 9 Pcs / mL; then add the liquid culture medium of each strain into different fermenters, and connect the bacteria in the triangular flask to the corresponding fermentor, and cultivate the bacteria in each fermentor at 28-30℃ Body content reaches 1.0×10 8 -1.0×10 9 Pcs / mL;
[0060] Step 2. Centrifugal separation and drying to obtain the microbial powder:
[0061] After centrifugal separation of the microbial bacteria liquid obtained by the expansion of the fermentor in step 1, the collected sedi...
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