Full biodegradation plastic for starch ester and preparation method
A technology for biodegradable plastics and starch esters, applied in the field of biodegradable plastics, can solve the problems of low degree of substitution of starch hydroxyl groups, and achieve the effects of excellent mechanical properties, excellent water resistance, and high reaction efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0033] 85 parts of tapioca starch, 5 parts of monopropyl maleate, 2 parts of succinic acid, 0.1 part of sodium tripolyphosphate, 0.05 part of lipase, and 200 parts of water were weighed for later use.
[0034] 1) Mix starch, water and lipase, raise the temperature in the reactor to 80°C, and stir at a constant speed for hydrolysis reaction for 30 minutes.
[0035] 2) The esterification agent succinic acid was added to the reaction kettle, the pressure of the reaction kettle was raised to 1.6Mpa, the temperature was raised to 120°C, and the esterification reaction was carried out under nitrogen protection for 30 minutes to obtain a liquid waxy starch ester.
[0036] 3) Add monopropyl maleate to the reaction kettle, the pressure of the reaction kettle rises to 1.6Mpa, the temperature rises to 120°C, and the polycondensation reaction occurs under nitrogen protection conditions to gradually form colloids. The reaction time is about 20 minutes, and the reaction is complete Finally,...
Embodiment 2
[0041] 90 parts of potato starch, 5 parts of ethyl dilactate, 2 parts of formic acid, 0.2 part of calcium maleate, 0.1 part of high-temperature α-amylase, and 200 parts of water were weighed for later use.
[0042] 1) Mix starch, water, and high-temperature α-starch in a reaction kettle at a temperature of 80°C, and stir at a constant speed for a hydrolysis reaction for 30 minutes.
[0043] 2) Formic acid was added to the reaction kettle, the pressure of the reaction kettle was raised to 2.0Mpa, the temperature was raised to 120°C, and the esterification reaction was carried out under nitrogen protection for 30 minutes to obtain a liquid waxy starch ester.
[0044] 3) Add ethyl dilactate into the reaction kettle, the pressure of the reaction kettle rises to 2.0Mpa, the temperature rises to 120°C, and the polycondensation reaction occurs under nitrogen protection conditions to gradually form colloids. The reaction time is about 20 minutes. After the reaction is complete, Add ca...
Embodiment 3
[0050] 95 parts of corn starch, 4 parts of hydroxybutyraldehyde, 3 parts of acetic anhydride, 0.2 part of epichlorohydrin, 0.1 part of high-temperature α-amylase, and 200 parts of water were weighed for later use.
[0051] 1) Combine starch, water, and high-temperature α-starch in a reaction kettle at a temperature of 80°C, and stir at a constant speed for a hydrolysis reaction for 40 minutes.
[0052] 2) Add acetic anhydride to the reactor, the pressure of the reactor is raised to 2.0Mpa, the temperature is raised to 120°C, and the esterification reaction is carried out under nitrogen protection for 30 minutes to obtain a liquid waxy starch ester.
[0053] 3) Add hydroxybutyraldehyde to the reaction kettle, the pressure of the reaction kettle rises to 2.0Mpa, and the temperature rises to 120°C. Under the condition of nitrogen protection, the polycondensation reaction gradually forms colloids. The reaction time is about 20 minutes. After the reaction is complete, add The epich...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
tensile strength | aaaaa | aaaaa |
tensile strength | 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