Preparation of cellulose carbamate and low-temperature dissolution spinning method of cellulose carbamate
A carbamate and low-temperature dissolving technology, applied in the direction of artificial filaments in cellulose solution, can solve the problems of low solubility and low solubility of cellulose, and achieve the effects of good filtration performance, improved solubility and good mechanical properties
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0025] A kind of preparation method of cellulose carbamate, it comprises the following steps:
[0026] (1) common cotton fiber (i.e. cellulose) and urea with a degree of polymerization between 300-600 are vacuum-dried at 70° C. for 24 hours;
[0027] (2) configuration concentration is the sodium hydroxide solution of 12-16%, gets a certain amount of cellulose and joins the sodium hydroxide solution, the cellulose addition is 5-10% of the sodium hydroxide solution quality, stirs evenly, at 50 Soak for 30-60 minutes at ℃;
[0028] (3) Take out the cellulose and wash it to neutral, and wash it until the water content is 200% to obtain alkalized cellulose, then add a certain amount of urea, the amount of urea added is 50-100% of the cellulose mass, stir evenly, put Heating in an oven at a reaction temperature of 120-140°C, reacting for 2-3 hours and drying to obtain cellulose carbamate.
[0029] A low-temperature solution-spinning method of cellulose carbamate, comprising the fo...
Embodiment 1
[0036] The cellulose and urea were vacuum dried at 70°C for 24 hours. Wherein, the cellulose is ordinary cotton fiber with a degree of polymerization of 300. Prepare 15kg of 16% sodium hydroxide aqueous solution, add 1.5kg of cellulose into the sodium hydroxide aqueous solution, stir evenly, soak at 50°C for 30 minutes, wash the cellulose to neutral after soaking, and obtain water-containing alkalized cellulose 3kg, then add 1.5kg urea and stir evenly, put it in an oven at 137°C and react for 2 hours, then dry until the quality of the reaction product remains unchanged, then pulverize the reaction product cellulose carbamate to obtain cellulose carbamate Ester powder, the particle size of which is 800 mesh.
[0037] Get 1kg of cellulose urethane powder and 10kg of solvent into the mixing tank through a metering pump (i.e. a cellulose meter) and stir for 15 minutes to mix evenly, then feed into a low-temperature co-rotating twin-screw extruder through a metering pump, extrude ...
Embodiment 2
[0043] The cellulose and urea were vacuum dried at 70°C for 24 hours. Wherein, the cellulose is common cotton fiber with a degree of polymerization of 400. Prepare 15kg of 14% sodium hydroxide aqueous solution, add 0.75kg of cellulose into the sodium hydroxide aqueous solution, stir evenly, soak at 50°C for 45 minutes, wash the cellulose to neutral after soaking, and obtain water-containing alkalized cellulose 1.5kg, then add 0.6kg urea and stir evenly, put it in an oven at 120°C for 3 hours and then dry it until the quality of the reaction product remains unchanged, then pulverize the reaction product cellulose carbamate to obtain cellulose carbamate Ester powder, the powder particle size is 600 mesh.
[0044] Get 1kg of cellulose urethane powder and 10kg of solvent into the mixing tank through a metering pump (i.e. a cellulose meter) and stir for 15 minutes to mix evenly, then feed into a low-temperature co-rotating twin-screw extruder through a metering pump, extrude Afte...
PUM
Property | Measurement | Unit |
---|---|---|
degree of polymerization | aaaaa | aaaaa |
stretch ratio | aaaaa | aaaaa |
degree of polymerization | 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