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Chitosan quaternary ammonium salt antibacterial fiber, fabric and hygienic product and their preparation processes

A chitosan quaternary ammonium salt and a technology for the preparation process, which can be used in fiber treatment, biochemical fiber treatment, textiles and papermaking, etc., can solve the problems of large differences in polarity, strong crystallinity of chitosan, and failure of synthesis, and achieve antibacterial properties. Improved performance, good cross-linking, good reactivity

Active Publication Date: 2017-02-22
QUANZHOU YALIN NEW MATERIAL TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Wang Xiaohua prepared an antibacterial finishing agent by degrading chitosan and reacting with isocyanate, but the author claimed that chitosan and isocyanate could not react homogeneously, and the synthesis failed
[0006] The current research issues are: 1. Chitosan has general antibacterial properties, and its antibacterial properties need to be improved
2. The polarity difference between chitosan and isocyanate is large, and they cannot be uniformly dispersed with each other, resulting in the agglomeration of the crosslinking agent. The crosslinking performance is general. 3. Chitosan has strong crystallinity. On the interface between the dispersed phase of polysaccharide and the dispersed phase of cross-linking agent, it cannot be deeply immobilized

Method used

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  • Chitosan quaternary ammonium salt antibacterial fiber, fabric and hygienic product and their preparation processes

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] 1. Add methyl ethyl ketone oxime to dry methyl ethyl ketone, and then slowly drop it into isophorone diisocyanate. Preferably, the ratio of mass parts of active hydrogen and -NCO is controlled to be n(H):n(NCO)=0.55:1, and the dropwise addition temperature is controlled not to exceed 40 degrees, then slowly heated to 80 degrees, cooled, and prepared for used for subsequent reactions at room temperature. The product in this step can be referred to as product one, and its degree of reaction can be measured by the di-n-butylamine method.

[0032] 2. Add 100ml of isopropanol, 5 grams of chitosan and appropriate amount of glycidyltrimethylammonium chloride into the three-necked bottle. Preferably, the mass ratio of chitosan and glycidyltrimethylammonium chloride is controlled to be 1:3-4, the reaction temperature is 70-80 degrees, and the time is 5-8 hours, and then it can be suction filtered, Wash thoroughly with ethanol and dry. The product in this step can be referred ...

Embodiment 2

[0035] The main difference between this embodiment and Embodiment 1 is that the chitosan quaternary ammonium salt antibacterial substance is liquid, that is, the chitosan quaternary ammonium salt antibacterial liquid. The chitosan quaternary ammonium salt antibacterial liquid preparation process can be prepared as an antibacterial agent by the process of Example 1, and then according to conventional methods, such as being dissolved in water and stirring to make a liquid chitosan quaternary ammonium salt antibacterial liquid. In addition, the chitosan quaternary ammonium salt antibacterial solution can also adopt the process in Example 1, only correspondingly omitting the steps of dehydration such as drying and drying. Other similarities will not be repeated here.

Embodiment 3

[0037] This embodiment is one of the specific applications of the first embodiment. The chitosan quaternary ammonium salt antibacterial agent (abbreviated as antibacterial agent) is dissolved in water, stirred, and the antibacterial agent is soaked in a ratio of 0.1-1% of the cloth weight and a bath ratio of 7-10, dehydrated, and dried at 90 degrees. Bake at 120 degrees for 30 minutes to get chitosan quaternary ammonium antibacterial fabric (abbreviated as antibacterial fabric). Preferably, the material is completely soaked for half an hour or several hours. The antibacterial performance test was carried out according to the FZ73023 standard, and the antibacterial rate of Escherichia coli was as follows after washing 50 times:

[0038] Sample serial number 1 2 3 Antibacterial rate 55.42 67.44 99.99

[0039]Sample 1 is chitosan and commercially available blocked isocyanate Bayer 3100; sample 2 is that chitosan does not carry out the quaternization of s...

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Abstract

The invention discloses a preparation process of chitosan quaternary ammonium salt antibacterial fiber, comprising: preparing chitosan and epoxypropyltrimethyl ammonium chloride into a chitosan quaternary ammonium salt with certain degree of substitution, reacting methyl ethyl ketoxime terminated isocyanate with the chitosan quaternary ammonium salt to obtain a reactive chitosan quaternary ammonium salt antibacterial agent or chitosan quaternary ammonium salt antibacterial liquid; dissolving the chitosan quaternary ammonium salt antibacterial agent or chitosan quaternary ammonium salt antibacterial liquid in water, and soaking the obtained fiber. The invention also discloses a chitosan quaternary ammonium salt antibacterial fabric and hygienic product and their preparation processes. Quaternary ammonium salt modified chitosan is synthesized herein, single-terminated isocyanate is introduced to the chitosan, the reactive quaternary ammonium salt chitosan has good antibacterial property far better than that of chitosan; by inoculating chitosan to isocyanate reaction groups, good reactiveness is provided; crystallinity of chitosan is decreased through quaternary ammonium salt salifying, it is possible for the isocyanate to react evenly with the fabric, the crosslinking effect is good, the antibacterial property of the fabric can be significantly improved, and the fabric has a promising application prospect.

Description

technical field [0001] The invention relates to a chitosan antibacterial substance, in particular to the specific application of a chitosan quaternary ammonium salt antibacterial substance. Background technique [0002] Chitosan is the product of deacetylation of chitin, and it is the most basic and important derivative of chitin. Chitin, also known as chitin and chitin, is chemically named (1,4)-2-acetamide-2-deoxy-β-D-glucan, and is mainly found in the shells of shrimp, crabs, pupae and insects. And in the cell walls of fungi and algae. The dry shell of arthropods contains about 20-50% chitin. There are three structures of chitin in nature: α, β, γ, among which the most common and common is the α type. The annual biosynthesis of chitin on the earth is billions of tons, and it is a natural polymer compound whose output is second only to cellulose. The structures of chitin and chitosan are as follows: [0003] [0004] In the pharmaceutical industry, surgical sutures...

Claims

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Application Information

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IPC IPC(8): D06M15/03C08B37/08
CPCC08B37/003D06M15/03D06M16/00
Inventor 庄跃林陈江枫
Owner QUANZHOU YALIN NEW MATERIAL TECH
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