Preparation method of long carbon chain dibasic acid
A technology of long-chain dibasic acid and production method, applied in the field of bioengineering, can solve the problems of slow development of downstream products of long-chain dibasic acid, backward production technology and equipment, and inability to meet customer needs, etc. The effect of cultivation process, shortened production cycle and low production cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] Fermentation control conditions:
[0048]Inoculum size: 8%, tank temperature: 25°C, ventilation ratio: 1:0.3vvm, tank pressure: 0.08Mpa, pH: 4.0 before adding alkanes, 6.5 after adding alkanes, culture time: 120 hours.
[0049] Feeding control parameters:
[0050] Alkanes: when the cell growth concentration is greater than (OD 620 ) 0.8, start to add cell regulator and alkane, add cell regulator once and add, control concentration of alkane in the fermentation broth is 3%, stop feeding 20 hours before the end of fermentation.
[0051] Extraction process of fermentation broth:
[0052] The fermented liquid is heated to 70°C by a steam heater and put into the fermented liquid storage tank. Afterwards, add liquid alkali to adjust the pH of the fermented liquid to 8.5 ~, separate the bacteria by membrane filtration, add 0.1% activated carbon to the dibasic acid clear liquid, decolorize at 50°C for 40 minutes, and then filter to obtain the decolorized clear liquid and aci...
Embodiment 2
[0056] Fermentation control conditions:
[0057] Inoculum size: 10%, tank temperature: 30°C, ventilation ratio: 1:0.5vvm, tank pressure: 0.10Mpa, pH: 5.0 before adding alkane, 7.5 after adding alkane, culture time: 140 hours.
[0058] Feeding control parameters:
[0059] Alkanes: when the cell growth concentration is greater than (OD 620 ) 0.8, start to add cell regulator and alkane, add cell regulator once and add, control concentration of alkane in the fermentation broth is 7%, stop feeding 20 hours before the end of fermentation.
[0060] Extraction process of fermentation broth:
[0061] The fermented liquid is heated to 70-90°C by a steam heater and put into the fermented liquid storage tank. Afterwards, add liquid alkali to adjust the pH of the fermentation broth to 9.5, separate the bacteria by membrane filtration, add 0.5% activated carbon to the dibasic acid clear liquid, decolorize at 65°C for 80 minutes, and then filter to obtain the decolorized clear liquid and ...
Embodiment 3
[0065] Fermentation control conditions:
[0066] Inoculum size: 20%, tank temperature: 35°C, ventilation ratio: 1:0.7vvm, tank pressure: 0.12Mpa, pH: 6.0 before adding alkane, 8.5 after adding alkane, culture time: 160 hours.
[0067] Feeding control parameters:
[0068] Alkanes: when the cell growth concentration is greater than (OD 620 ) 0.8, start to add cell regulator and alkane, add cell regulator once and add, control concentration of alkane in the fermentation broth is 10%, stop feeding 20 hours before the end of fermentation.
[0069] Extraction process of fermentation broth:
[0070] The fermented liquid is heated to 70-90°C by a steam heater and put into the fermented liquid storage tank. Afterwards, add liquid alkali to adjust the pH of the fermentation broth to 10.5, separate the bacteria by membrane filtration, add 1.0% activated carbon to the dibasic acid clear liquid, decolorize at 80°C for 120 minutes, and then filter to obtain the decolorized clear liquid a...
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