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

Preparation method of cross-linked amphoteric bagasse xylan

A technology of xylan and bagasse, applied in the field of preparation of cross-linked amphoteric bagasse xylan, achieving high application value

Active Publication Date: 2013-01-16
GUILIN UNIVERSITY OF TECHNOLOGY
View PDF3 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, most of the research on the functional modification of xylan at home and abroad uses xylan from birch, beech, corn cob and other sources as raw materials, and there are few reports on the modification of xylan from bagasse from agricultural and forestry waste.

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
  • Preparation method of cross-linked amphoteric bagasse xylan
  • Preparation method of cross-linked amphoteric bagasse xylan
  • Preparation method of cross-linked amphoteric bagasse xylan

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] (1) Dry bagasse xylan in a vacuum oven at 60°C to constant weight to obtain powdery dry basis bagasse xylan.

[0047] (2) Weigh 12 g of powdery dry-based bagasse xylan and 25 g of deionized water obtained in step (1) into the reactor, stir and mix at room temperature to obtain a xylan suspension with a mass fraction of 32.43%.

[0048] (3) Weigh 0.9g of sodium hydroxide and dissolve it in 6.0mL of deionized water, add it to the xylan suspension obtained in step (2); adjust the pH of the system to 9 with a concentration of 3.0mol / L hydrochloric acid, stir and activate for 1.5 hours .

[0049] (4) Dissolve 1.2g of esterifying agent succinic anhydride in 20mL of ethanol with a volume fraction of 95% to obtain succinic anhydride ethanol solution;

[0050] (5) Weigh 0.1g catalyst 12-tungstophosphoric acid into the system obtained in step (3), control the reaction temperature at 40±2°C, and add the succinic anhydride ethanol solution obtained in step (4) into step (3) in thr...

Embodiment 2

[0060] (1) Dry bagasse xylan in a vacuum oven at 60°C to constant weight to obtain powdery dry basis bagasse xylan.

[0061] (2) Weigh 15 g of powdery dry-based bagasse xylan and 28 g of deionized water obtained in step (1) into the reactor, stir and mix at room temperature to obtain a xylan suspension with a mass fraction of 34.88%.

[0062] (3) Dissolve 1.2g of sodium hydroxide in 15mL of deionized water and add it to the xylan suspension obtained in step (2); adjust the pH of the system to 10 with 3.0mol / L hydrochloric acid, and stir for 1.5 hours to activate.

[0063] (4) Dissolve 2.0 g of esterifying agent succinic anhydride in 40 mL of ethanol with a volume fraction of 95% to obtain succinic anhydride ethanol solution.

[0064] (5) Weigh 0.3g catalyst 12-tungstophosphoric acid into the system obtained in step (3), control the reaction temperature at 60±2°C, add the succinic anhydride ethanol solution obtained in step (4) into step (3) in three batches at intervals of 20 ...

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 discloses a preparation method of cross-linked amphoteric bagasse xylan. By using bagasse xylan as the initial raw material, deionized water as a solvent, 3-chloro-2-hydroxypropyltrimethylammonium chloride as a cationic reagent, succinic anhydride as an anionic reagent, glyoxal as a cross-linking agent and 12-tungstophosphoric acid as a catalyst, the bagasse xylan is subjected to chemical modification by etherification, esterification and cross-linking to obtain the cross-linked amphoteric bagasse xylan. The product has multiple structures and characteristics of anionic xylan, cationic xylan, natural high molecular polymers and the like. After the cross-linking, the alocholic hydroxtyl group of the amphoteric xylan and the multielement functional group of the cross-linking agent form a diether bond or diester bond, or two or more amphoteric xylan molecules form a bridge, thereby forming the multidimensional network structure. Compared with bagasse xylan, the heat stability and hydrophobicity of the cross-linked amphoteric bagasse xylan prepared by the method disclosed by the invention are obviously improved; and compared with the single-modified xylan derivative, the cross-linked amphoteric bagasse xylan has better service performance.

Description

technical field [0001] The invention relates to a preparation method of cross-linked amphoteric bagasse xylan. Background technique [0002] Xylan is widely distributed in nature, second only to fiber, starch and other natural polymer compounds. It is a common component in higher plants and one of the main forms of carbohydrate storage. Its major advantage is Both biodegradable and renewable. Guangxi is an area rich in bagasse in China, and the content of xylan in bagasse is about 30%. With the increasing emphasis on renewable resources and green chemical industry, how to modify the natural xylan extracted from bagasse, introduce new functional groups, and increase and expand the use of xylan has become an important topic of increasing concern. It is a meaningful work to use xylan, a renewable resource, to study new chemical products with better performance and wider use. [0003] At present, most studies on the functional modification of xylan at home and abroad use xyla...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C08B37/00
Inventor 李和平胡杨杨官威杨永哲张垚黄云燕袁金伟
Owner GUILIN UNIVERSITY OF TECHNOLOGY
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