Composite microbial agent preparation device and method for river pollution control
A compound microbial agent and preparation device technology, which is applied in the field of river pollution control, can solve the problems of long treatment time, complex components of polluted water, large dosage, etc., achieve efficient treatment and improve the effect of physiological activity function
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Embodiment 1
[0054] Such as figure 1 Shown, a kind of preparation device and method of composite microbial bacterial agent for river pollution control, its preparation device comprises slope culture device 1, shake flask culture device 2, primary seed small tank 3, primary batching tank 4, primary Small seed tank pH regulator 5; secondary seed tank 6, secondary batching tank 7, secondary seed tank pH regulator 8; fermentation tank 9, fermentation tank feed tank 10, fermentation tank pH regulator 11, fermentation tank ingredients Tank 12; liquid packaging device 13, inclined tube sedimentation tank 14, diaphragm pump 15, plate and frame filter press 16, double drum filter press 16, double drum dryer 17, pulverizer 18, solid packaging device 19; sterile filtration Back steam main pipe 20, air main pipe 21 after sterilization filtration.
[0055] The slope culture device 1 is a test tube slope, and there are 6 sets of slopes in total.
[0056] The shaking flask culture device 2 is a triangu...
Embodiment 2
[0077] A method for preparing a compound microbial agent preparation device for river pollution, comprising the steps of:
[0078] 1. Preparation method
[0079] a) Strains
[0080] Pseudomonas pseudoalcaligenes, Nitrobacter, Nitrosococcus, Bacillus subtilis, Clostridium, Lactobacillus curvatus.
[0081] b) Slant 1 strain activation
[0082] Slant 1 seed medium composition: beef extract 1%, peptone 1%, Nacl 0.5%, glucose 0.5%, agar 2% (above is the volume fraction), pH7.2~7.5. Sterilized at 0.1Mpa.30min, and kept at 30°C for 24h.
[0083] Streak inoculation of the preserved strains of the above 6 strains on the slant seed medium of the respective strain test tubes by streak inoculation, and culture at 30~32°C for 18~24h to activate the above 6 strains.
[0084] c) Shake flask 2 culture
[0085] Shake Flask 2 Seed Medium Composition: Glucose 3.0%, (NH 4 ) 2 SO 4 0.5%, K 2 HPO 4 0.2%, corn syrup 2~3%, peanut cake hydrolyzate 2~3%, MgSO 4 ·7H 2 O0.06~0.08%, urea 0.2% ...
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