Hyperbranched ammonium salt type cationic surface active agent and preparation and application
A surfactant and cationic technology, which is applied in the field of hyperbranched ammonium salt cationic surfactant and synthesis, can solve the problems of particle re-aggregation or precipitation, weak adsorption of solid particles, poor system stability, etc., and achieve the goal of promoting homogeneity Formation, good dispersion effect, effect under mild conditions
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0045] 1) Synthesis of hyperbranched ammonium salt cationic surfactants.
[0046] Phenol and oxalic acid, which is 1% by mass percentage based on the total amount of monomers, are added to the reaction flask, and nitrogen protection is introduced, and the temperature is raised to 100° C. under stirring, and styrene is slowly added dropwise (the molar ratio of styrene to phenol is 1: 1.5), reacted for 4 hours, stopped the reaction and cooled to room temperature to obtain 4-phenethylphenol with a yield of 94%.
[0047] Add 4-phenethylphenol and triethylamine with a mass percentage of 4% based on the total amount of monomers into the reaction flask, dissolve in absolute ethanol that is 5 times the total weight of the monomers, and heat up to 80°C under stirring , slowly drop epichlorohydrin (the molar ratio of 4-phenethylphenol to epichlorohydrin is 1:1.1), react for 4h, stop the reaction and cool to room temperature, that is, 1-cyclopropylmethoxy-4- Phenylethylbenzene, yield 90...
Embodiment 2
[0064] Phenol and 1% concentrated phosphoric acid based on the total amount of monomers were added to the reaction flask, and nitrogen protection was introduced, and the temperature was raised to 100°C under stirring, and styrene was slowly added dropwise (the molar ratio of styrene to phenol was 1 : 1.5), reacted for 4h, stopped the reaction and cooled to room temperature to obtain 4-phenethylphenol with a yield of 98%.
[0065] Add 4-phenethylphenol and potassium carbonate with a mass percentage of 4% based on monomers into the reaction flask, dissolve in absolute ethanol that is 5 times the total mass of the monomers, heat up to 80°C under stirring, and slowly drop Add epichlorohydrin (the molar ratio of 4-phenethylphenol to epichlorohydrin is 1:1.1), react for 4 hours, stop the reaction and cool to room temperature to obtain 1-cyclopropylmethoxy-4-phenethyl Benzene, yield 92%.
[0066] Dissolve polyethyleneimine in acetone 5 times the total mass of the monomers, add it to...
Embodiment 3
[0070] Phenol and 1% concentrated nitric acid based on the total amount of monomers were added to the reaction flask, and nitrogen protection was introduced, and the temperature was raised to 100°C under stirring, and styrene was slowly added dropwise (the molar ratio of styrene to phenol was 1 : 1.5), reacted for 5h, stopped the reaction and cooled to room temperature to obtain 4 phenethylphenol with a yield of 98%.
[0071] Add 4-phenethylphenol and potassium hydroxide with a mass percentage of 4% based on the total amount of monomers into the reaction flask, dissolve in absolute ethanol that is 5 times the total weight of the monomers, and heat up to 80°C under stirring , slowly drop epichlorohydrin (the molar ratio of 4-phenethylphenol to epichlorohydrin is 1:1.1), react for 4h, stop the reaction and cool to room temperature, that is, 1-cyclopropylmethoxy-4- Phenylethylbenzene, yield 90%.
[0072] Dissolve polyethyleneimine in acetone 5 times the total mass of the monomer...
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