Rapid urokinase absorption bag
An adsorption bag, urokinase technology, applied in the field of separation and purification, can solve the problems of inconvenient collection and transportation of raw materials, difficult to achieve large-scale production, and the need for pressurized equipment, reducing the collection of raw urine, facilitating large-scale industrial production, cost saving effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0034] (1) Take 50g of absorbent cotton, add 46g of sodium hydroxide, 600ml of water, and stir at 37°C for 2 hours. Then, 60 g of monochloroacetic acid was added and stirred at 75°C for 4 hours. After the reaction product was separated, it was repeatedly rinsed with pure water to neutrality, then rinsed with absolute ethanol for 3 times, and dried in vacuum to obtain modified absorbent cotton fibers.
[0035] (2) Take the raw silica gel, soak it in 300ml 6mol / L hydrochloric acid solution for 4 hours, wash until there is no chloride ion, and dry it at 130°C for 2 hours. Activate 50g of dried silica gel in a muffle furnace at 250°C for 4 hours, add 200ml of toluene and 20g of phenyltrichlorosilane, reflux and stir for 24 hours, filter after the reaction, wash with toluene, acetone and methanol in sequence, and dry to obtain Precursor. Take 50g of precursor silica gel and put it into a beaker, add 200ml of 98% concentrated sulfuric acid, sulfonate at 100°C for 2 hours, filter th...
Embodiment 2
[0038](1) Take 30g of absorbent cotton, add 21.6g of sodium hydroxide, 720ml of water, and stir at 30°C for 3 hours. Then, 108 g of monochloroacetic acid was added and stirred at 70°C for 5 hours. After the reaction product was separated, it was repeatedly rinsed with pure water to neutrality, then rinsed with absolute ethanol for 3 times, and dried in vacuum to obtain modified absorbent cotton fibers.
[0039] (2) Take the raw silica gel, soak it in 500ml 4mol / L hydrochloric acid solution for 5 hours, wash until there is no chloride ion, and dry it at 120°C for 3 hours. Activate 50g of dried silica gel in a muffle furnace at 200°C for 6 hours, add 100ml of toluene and 35g of phenyltrichlorosilane, reflux and stir for 10 hours, filter after the reaction, wash with toluene, acetone and methanol in sequence, and dry to obtain Precursor. Take 50g of the precursor silica gel and put it into a beaker, add 500ml of 98% concentrated sulfuric acid, sulfonate it at 90°C for 5 hours, f...
Embodiment 3
[0042] (1) Take 50g of absorbent cotton, add 200g of sodium hydroxide, 400ml of water, and stir at 40°C for 2 hours. Then add 60 g of monochloroacetic acid and react at 80° C. for 3 hours. After the reaction product is separated, it is repeatedly washed with pure water to neutrality, then washed with absolute ethanol for 3 times, and vacuum-dried to obtain the modified absorbent cotton fiber.
[0043] (2) Take the raw silica gel, soak it in 100ml of 8mol / L hydrochloric acid solution for 3 hours, wash until there is no chloride ion, and dry at 140°C for 1 hour. Activate 50g of dried silica gel in a muffle furnace at 300°C for 2 hours, add 500ml of toluene and 50g of phenyltrichlorosilane, reflux and stir for 40 hours, filter after the reaction, wash with toluene, acetone and methanol in sequence, and dry to obtain Precursor. Take 50g of the precursor silica gel and put it into a beaker, add 350ml of 98% concentrated sulfuric acid, sulfonate it at 110°C for 2 hours, filter thro...
PUM
Property | Measurement | Unit |
---|---|---|
pore size | aaaaa | aaaaa |
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