Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Beta-caryophyllene-maleic anhydride copolymer as well as preparation method and application thereof

A kind of technology of maleic anhydride and caryophyllene, applied in the field of beta-caryophyllene-maleic anhydride copolymer and preparation thereof, can solve the problems that do not involve beta-caryophyllene-maleic anhydride and the like, achieve mild conditions and operating costs Low, simple post-processing effects

Active Publication Date: 2016-07-27
INST OF CHEM IND OF FOREST PROD CHINESE ACAD OF FORESTRY
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, none of these methods involved β-caryophyllene-maleic anhydride copolymers

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Beta-caryophyllene-maleic anhydride copolymer as well as preparation method and application thereof
  • Beta-caryophyllene-maleic anhydride copolymer as well as preparation method and application thereof
  • Beta-caryophyllene-maleic anhydride copolymer as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Add 10.38 g of β-caryophyllene, 4.90 g of maleic anhydride, 0.584 g of di-tert-butyl peroxide and 30.6 g of cyclohexanone into a 100 ml three-necked flask equipped with a thermometer and a magnetic stirring bar. Under the protection of nitrogen, raise the temperature to 150°C, react for 1 hour, then stop the reaction, pour the reactant into a large amount of methanol, a white precipitate is precipitated, and then perform suction filtration to obtain a white powdery solid. After drying, the measured mass is 11.1g , yield 72.63%. The molecular weight of the copolymer measured by GPC M n for 1404, M w for 3249. Then get 2g copolymer and join in the one-necked flask that the NaOH solution of 5% mass fraction is housed, heat and reflux to transparent, then pour the reactant into a large amount of methanol to separate out a white precipitate, suction filter, and dry to obtain a saponified product. The surface tension of the object was measured, and the results are shown in...

Embodiment 2

[0036] 10.38 g of β-caryophyllene, 4.90 g of maleic anhydride, 0.438 g of di-tert-butyl peroxide and 22.93 g of cyclohexanone were added. Under the protection of nitrogen, the temperature was raised to 145° C., and the reaction was carried out for 1 hour. The other conditions were the same as in Example 1. The quality of the finally obtained copolymer was 11.1 g, and the yield was 79.83%.

Embodiment 3

[0038] 10.38 g of β-caryophyllene, 4.90 g of maleic anhydride, 0.584 g of di-tert-butyl peroxide and 30.57 g of cyclohexanone were added. Under the protection of nitrogen, the temperature was raised to 150° C., and the reaction was carried out for 10 minutes. The other conditions were the same as in Example 1. The quality of the finally obtained copolymer was 9.6 g, and the yield was 62.81%.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a beta-caryophyllene-maleic anhydride copolymer as well as a preparation method and an application thereof. The copolymer contains acid anhydride bonds and is prepared from beta-caryophyllene and maleic anhydride through copolymerization. Beta-caryophyllene and maleic anhydride in the ratio being 4:1-1:6 are dissolved in a solvent or directly subjected to bulk mixing under protection of nitrogen, a radical initiator is added, and then the beta-caryophyllene-maleic anhydride copolymer is obtained through a reaction under a heating condition. The beta-caryophyllene-maleic anhydride copolymer can be widely applied to industries such as paint, cosmetics, food and the like. An anionic surfactant is obtained through saponification of the beta-caryophyllene-maleic anhydride copolymer. The reaction conditions are mild, the process is simple, and industrial production is easy.

Description

technical field [0001] The invention relates to polymer preparation, in particular to a β-caryophyllene-maleic anhydride copolymer and its preparation method and application. technical background [0002] my country's masson pine resin output is large, ranking first in the world. Masson pine resin is distilled to obtain light turpentine, heavy turpentine and rosin. At present, there are many studies on light turpentine and rosin, and there are many industrialized products, but the research on heavy turpentine is still relatively scarce, and there are not many industrialized products, resulting in the price of heavy turpentine has been in a downturn. The main components of heavy turpentine are longifolene and β-caryophyllene. Among them, the content of β-caryophyllene can reach about 19%. The research and utilization of β-caryophyllene is of great significance for improving the refined utilization rate of heavy turpentine. [0003] β-Caryophyllene belongs to bicyclic sesqu...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08F232/08C08F222/06C08F8/42
CPCC08F8/42C08F232/08C08F222/06
Inventor 陈玉湘闵邓昊赵振东卢言菊徐士超毕良武王婧古研
Owner INST OF CHEM IND OF FOREST PROD CHINESE ACAD OF FORESTRY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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