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Preparation method for chelate ion-exchange fiber

A technology for exchanging fibers and chelating ions, which is applied in the ion exchange of chelates, ion exchange, fiber treatment, etc., and can solve the problems of removal and recovery, lower utilization rate of 5-chloromethyl salicylaldehyde, retention, etc.

Inactive Publication Date: 2012-07-04
HUAIHAI INST OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, during the reaction process between the functional fiber coated with amino resin and 5-chloromethyl salicylaldehyde, not only the tertiary amino group and 5-chloromethyl salicylaldehyde undergo nucleophilic reaction, but also the hydroxyl groups on the surface of the substrate fiber It can undergo nucleophilic reaction with 5-chloromethyl salicylaldehyde, and the microporous capillary action of the substrate fiber and the hydrogen bond of the hydroxyl group on the substrate fiber to 5-chloromethyl salicylaldehyde will retain the 5-chloromethyl salicylaldehyde that has not undergone nucleophilic reaction. Chloromethyl salicylaldehyde, the washing and extraction of post-treatment organic solvents alone cannot completely remove and recycle excess 5-chloromethyl salicylaldehyde that did not participate in the reaction, resulting in 5-chloromethyl salicylaldehyde lower utilization of

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] The preparation method and application of embodiment 1 cotton-polyester blended yarn-1.

[0024] Step 1, preparation of quaternary amino functional resin solution

[0025] Weigh 56 grams of 5-chloromethyl salicylaldehyde and dissolve it in 200 grams of 1,4-dioxane, mix it with dimethylaminoethyl methacrylate / methyl methacrylate / styrene / maleic dioxane Acid anhydride / ethylene glycol dimethacrylate is solution polymerized in 300 grams of 1,4-dioxane according to the mass ratio of 50:15:15:10:10. The amino-based functional resin solution is controlled at a temperature of 20 ~ 25°C, reacted for 2 hours, then raised the temperature to 60-65°C, reacted for 10 hours, cooled to room temperature, and obtained 655 grams of light yellow quaternary amino functional resin solution.

[0026] Step 2, the preparation of quaternary ammonium-based cotton-polyester blended yarn

[0027] Put 100 grams of commercially available 18S natural color cotton-polyester 55 / 45 blended yarn in the q...

Embodiment 2

[0031] Preparation and application of embodiment 2 chelating ion exchange cotton-polyester blended yarn-②

[0032] According to the method and operation steps of Example 1, the thiosemicarbazide in Step 1 of Example 1 was replaced with anthranilic acid to obtain orange-red chelated ion-exchanged polyester-cotton blended yarn-②.

[0033] Take by weighing 10.00 grams of dry chelated ion-exchanged cotton-polyester blended yarn-②, immerse in 2000 milliliters of pH=6 in the 0.02mol / L zinc chloride aqueous solution, after 30 minutes (at this time the chelated ion-exchanged cotton-polyester blended yarn -② from orange red to bright red), use deionized water to wash the chelated ion exchange cotton polyester blended yarn -② to neutral, dry, the weight gain is 1.838 grams, after calculation, the multifunctional chelated ion exchange cotton polyester The retained adsorption capacity of the blended yarn (1) to zinc chloride was 1.351 mmol / g.

Embodiment 3

[0034] Preparation and application of embodiment 3 chelating ion exchange cotton-polyester blended yarn-③

[0035] According to the method and operation steps of Example 1, the thiosemicarbazide in Step 1 of Example 1 was replaced with 2-pyridinecarbohydrazide to obtain light yellow chelated ion exchange polyester-cotton blended yarn-③.

[0036] Take by weighing 10.00 grams of dry chelated ion-exchanged cotton-polyester blended yarn-③, immerse in the 0.02mol / L zinc chloride aqueous solution of 2000 milliliters of pH=6, after 30 minutes (this moment chelated ion-exchanged cotton-polyester blended yarn -③ from light yellow to bright green yellow), use deionized water to wash the chelated ion exchange cotton polyester blended yarn -③ to neutral, dry, the weight gain is 2.032 grams, after calculation, the chelated ion exchange cotton polyester blended yarn The retained adsorption capacity of yarn-③ on zinc chloride is 1.494mmol / g.

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PUM

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Abstract

The invention provides a preparation method for a chelate ion-exchange fiber. The preparation method comprises the following steps: finishing the nucleophilic reaction of amido functional resin and 5-chloromethyl salicylaldehyde in a solution in advance, thereby obtaining a quaternary amine functional resin solution; coating a substrate fiber, thereby obtaining a quaternary amine functional fiber; and performing the condensation reaction of the quaternary amine functional fiber and the amino compound, thereby finally obtaining the chelate ion-exchange fiber with a quaternary amine and salicylaldehyde peptide compound structural unit linked with the surface layer. According to the preparation method, the possibility of reaction between the 5-chloromethyl salicylaldehyde and the substrate fiber is avoided, the physical adsorption of the substrate fiber to the 5-chloromethyl salicylaldehyde is eliminated, and the local reaction selectivity and the use ratio of the 5-chloromethyl salicylaldehyde are increased.

Description

technical field [0001] The invention relates to a chelating ion exchange fiber, in particular to a chelating ion exchange fiber formed by coating the fiber with a chelating resin, and belongs to the field of functional materials. technical background [0002] The existing methods for preparing chelated ion exchange fibers mainly include: one is the chemical modification of the base fiber, so that the base fiber has ion adsorption capacity and ion chelation capacity. However, after the base fiber is chemically modified, some mechanical properties are significantly deteriorated, which affects the processing performance and use performance of the chelated ion exchange fiber. The second is the copolymerization resin spinning of the functional monomer and the second monomer, or the graft copolymerization of the functional monomer to the base fiber. However, most of the functional monomers are complex or expensive in synthesis technology, and the functional resins are difficult t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): D06M15/267D06M13/435D06M11/155D06M13/342D06M13/422B01J45/00
Inventor 斯琴高娃韩桂泉刘霖张田林
Owner HUAIHAI INST OF TECH