Preparation method of household antibacterial carpet
An antibacterial carpet and household technology, which is applied in the biochemical treatment of velvet protectant/mothproof agent, textile and papermaking, fiber treatment, etc. Good antibacterial effect, good biocidal effect
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[0018] The invention provides a kind of preparation method of antibacterial agent, comprising the following steps: dissolving cyanuric chloride in acetone, stirring, then dropwise adding the acetone solution of 4-amino-2,2,6,6-tetramethylpiperidine, Adjust the pH value to 7, stir to obtain a mixed solution; heat the mixed solution to 45°C, add dropwise an aqueous solution of N-(2-aminoethyl)pyridinium chloride, react for 1-3 hours, and adjust the pH value to 6. Filter to obtain the antibacterial agent.
[0019] As a preferred solution, the mass ratio of cyanuric chloride to 4-amino-2,2,6,6-tetramethylpiperidine is 90-100:7-8.
[0020] The N-(2-aminoethyl)pyridinium chloride was prepared according to the following method: 2-chloroethylamine hydrochloride, pyridine and water were mixed, stirred and refluxed for 1 hour, extracted with toluene; the aqueous layer was extracted with concentrated hydrochloric acid The pH value was adjusted to 3, then the solvent was evaporated, and ...
Embodiment 1
[0033] Preparation of antibacterial agent:
[0034] Step 1) Synthesis of N-(2-aminoethyl)pyridinium chloride
[0035] In a 25L round bottom flask, 1.16kg of 2-chloroethylamine hydrochloride and 2.77kg of pyridine were mixed, and then 1L of water was added. The mixture was stirred and heated to reflux for 1 hour, then the mixture was cooled to room temperature and extracted three times with 1 L of toluene. Among them, the molar ratio of 2-chloroethylamine hydrochloride:pyridine is 1:3.5. The pH of the aqueous layer was adjusted to 3 with concentrated hydrochloric acid, then the solvent was evaporated and the crude product was obtained using a rotary evaporator under vacuum. After purification with isopropanol, N-(2-aminoethyl)pyridinium chloride was collected by filtration in 92% yield.
[0036] Step 2) Synthesis of triazine-based quaternized N-halamines
[0037] 922.g of cyanuric chloride was dissolved in 1L of acetone and stirred at 10°C for 10 minutes. Then, 78 g of 4-a...
Embodiment 2
[0041] The fabric carpet is dipped into the final solution triazine-based quaternized N-halamine. After 10 minutes of treatment at 70°C, the temperature was raised to 80°C and a small amount of sodium hydroxide was added. The reaction was left for 1 hour, and the fabric was removed, rinsed thoroughly with tap water, and dried at 60°C.
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