Culturing method for dominant nitrosation bacterial community
A technology of dominant flora and culture method, applied in biochemical equipment and methods, adding compounds to stimulate growth, microorganisms, etc., can solve the problems of difficult and stable control of DO concentration, long time, and ineffective control, and achieve long-term The effect of stabilizing nitrosation ability, strong bacterial tolerance, and shortening the culture time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] The first stage: the enrichment of nitrifying bacteria, the initial ammonia nitrogen concentration of the culture solution is 150mg / L, and NaHCO is used during the enrichment process 3 The solution adjusts the pH value. Culture conditions: temperature is 24℃, pH is 6.0-7.5, SV30 is 15%-20%, DO is 4mg / L. One cycle per day, water intake time is 20 minutes, aeration is 23 hours, natural sedimentation is 30 minutes, and the supernatant is removed. Then add the same volume of the enriched culture medium as the supernatant, and add the microbial growth promoter A-I at the concentration of 20 mg / L of the promoter in the sewage every time the culture medium is replaced. Follow this process to cycle operation, using GB7479 distillation The titration method detects the ammonia nitrogen concentration in the water. After the ammonia nitrogen is not detected, increase the ammonia nitrogen concentration pre-added to the culture solution by 100 mg / L. After 15 days, a mixed flora with a...
Embodiment 2
[0036] The first stage: the enrichment of nitrifying bacteria. The initial ammonia nitrogen concentration of the culture solution is 150mg / L. During the enrichment process, NaHCO is used 3 The solution adjusts the pH value. Culture conditions: temperature is 24℃; pH is 6.0-7.5; SV is 15%-20%; DO is 4mg / L. One cycle per day, water intake time is 20 minutes, aeration is 23 hours, natural sedimentation is 30 minutes, and the supernatant is removed. Then add the same volume of the enriched culture medium as the supernatant, and add the microbial growth promoter A-II according to the concentration of the promoter in the sewage 25mg / L each time the culture medium is replaced, and the cycle operation is performed according to this process, using GB7479 distillation The titration method detects the concentration of ammonia nitrogen in the water. After the ammonia nitrogen is not detected, increase the concentration of ammonia nitrogen pre-added to the culture solution by 100 mg / L. Afte...
Embodiment 3
[0040] The first stage: the enrichment of nitrifying bacteria. The initial ammonia nitrogen concentration of the culture solution is 150mg / L. During the enrichment process, NaHCO is used 3 The solution adjusts the pH value. Culture conditions: temperature is 24℃; pH is 6.0-7.5; SV is 15%-20%; DO is 4mg / L. One cycle per day, water intake time is 20 minutes, aeration is 23 hours, natural sedimentation is 30 minutes, and the supernatant is removed. Then add the same volume of the enriched culture medium as the supernatant. Each time the culture medium is replaced, the microbial growth promoter A-Ⅲ must be added according to the concentration of the promoter in the sewage 25mg / L, and the cycle operation is carried out according to this process, using GB 7479 Distillation titration method detects the ammonia nitrogen concentration in the water. After the ammonia nitrogen is not detected, increase the ammonia nitrogen concentration pre-added to the culture solution by 100 mg / L. After...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com