Method for preparing sodium diacetate
A technology of sodium diacetate and preparation steps, which is applied in the field of preparation of sodium diacetate, can solve problems such as unstable product quality, difficult recovery of mother liquor, long reaction time, etc., achieve stable product quality, simple and easy operation, and reduce production cost Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
example 1
[0020] First in parts by weight, get 40 parts of PDA medium, 5 parts of glucose solution with a mass fraction of 15%, 16 parts of starch and 2 parts of urea, mix evenly, use phosphoric acid with a mass fraction of 10% to adjust the pH to 4.0, and Sterilize in a sterilizing furnace to obtain a medium, inoculate Aspergillus Usami into the medium according to the inoculum size of 12%; then move the above inoculated medium to a constant temperature incubator, set the temperature at 28°C, and cultivate After 6 days, the culture medium was taken out, and the surface of the culture medium was rinsed with water for 3 minutes, and the eluate was collected to obtain a mycelium suspension; then, according to the solid-to-liquid ratio of 1:2, sodium carbonate and the above-mentioned mycelia suspension were put into a glass In the reaction kettle, use nitrogen to exhaust the air in the glass reaction kettle, irradiate the glass reaction kettle with β rays for 50s, then stir at 120r / min for ...
example 2
[0023] First, in parts by weight, get 43 parts of PDA medium, 8 parts of glucose solution with a mass fraction of 15%, 20 parts of starch and 2.5 parts of urea, mix evenly, use phosphoric acid with a mass fraction of 10% to adjust the pH to 4.3, and Sterilize in a sterilizing furnace to obtain a culture medium, inoculate Aspergillus Usami into the culture medium according to the inoculum size of 14%; then move the above inoculated culture medium to a constant temperature incubator, set the temperature to 30°C, and cultivate After 7 days, the medium was taken out, and the surface of the medium was rinsed with water for 4 minutes, and the eluate was collected to obtain a suspension of mycelium; then, according to a solid-to-liquid ratio of 1:2, put sodium carbonate and the suspension of mycelia obtained above into a glass In the reactor, use nitrogen to exhaust the air in the glass reactor, irradiate the glass reactor with β-rays for 60s, then stir at 120r / min for 1.5h at room te...
example 3
[0026]First in parts by weight, get 45 parts of PDA medium, 10 parts of glucose solution with a mass fraction of 15%, 24 parts of starch and 3 parts of urea, mix evenly, use phosphoric acid with a mass fraction of 10% to adjust the pH to 4.5, and Sterilize in a sterilizing furnace to obtain a culture medium, inoculate Aspergillus Usami into the culture medium according to the inoculum size of 16%; then move the above-mentioned inoculated culture medium to a constant temperature incubator, set the temperature to 32°C, and cultivate After 9 days, the culture medium was taken out, and the surface of the culture medium was rinsed with water for 5 minutes, and the eluent was collected to obtain a suspension of mycelia; after that, sodium carbonate and the suspension of mycelia obtained above were put into a glass with a solid-to-liquid ratio of 1:2. In the reactor, use nitrogen to exhaust the air in the glass reactor, irradiate the glass reactor with β-rays for 70s, then stir at 120...
PUM

Abstract
Description
Claims
Application Information

- R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com